D02.04 - Hydrocarbon Analysis

SIGNIFICANCE AND USE
5.1 A knowledge of the hydrocarbon composition of the middle distillates, including the biodiesel blends is useful in following the effect of changes in process variables, diagnosing the source of plant upsets, and in evaluating the effect of changes in composition on product performance properties. The total aromatics content and polycyclic aromatics content are also important to evaluate the quality of diesel fuels/biodiesel blends. It requires an appropriate analytical method to make such determinations for diesel fuel/biodiesel blends production process and quality control.  
5.2 This test method provides a comprehensive analytical strategy for the determination of the total aromatics contents, polycyclic aromatics contents and the detail hydrocarbon composition of diesel fuel/biodiesel blends to ensure compliance with certain specifications or regulations.  
5.3 Test Method D2425 is applicable to the determination of the detailed hydrocarbon composition in middle distillates, however, the pre-separation procedure of elution chromatography is time-consuming and not eco-friendly. By combining with the separation procedures described in Test Method D8144, the dual column GC-MS system proposed in this method can determine the total aromatic hydrocarbon contents, polycyclic aromatic hydrocarbon contents and detailed hydrocarbon composition of diesel fuel/biodiesel blends simultaneously. The content of FAME in biodiesel blends can also be determined by GC. It is demonstrated to be time-saving and eco-friendly for the quality control of diesel fuel and biodiesel blends.
SCOPE
1.1 This test method covers an analytical scheme using the gas chromatography/mass spectrometry (GC-MS) to determine the hydrocarbon types present in middle distillates 170 °C to 365 °C boiling range, 5 % to 95 % by volume as determined by Test Method D86, including biodiesel blends with up to 20 % by volume of fatty acid methyl ester (FAME). The detailed hydrocarbon composition, total aromatic hydrocarbon and polycyclic aromatic hydrocarbon contents can be determined. The hydrocarbon types include: paraffins, noncondensed cycloparaffins, condensed dicycloparaffins, condensed tricycloparaffins, alkylbenzenes, indans or tetralins, or both, CnH2n-10 (indenes, etc.), naphthalenes, CnH2n-14 (acenaphthenes, etc.), CnH2n-16 (acenaphthylenes, etc.), and tricyclic aromatics. The content of FAME in biodiesel blends can also be determined by GC.  
1.2 The values stated in acceptable SI units are to be regarded as the standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The determination of class group composition of aviation turbine fuels is useful for evaluating quality and expected performance, as well as compliance with various industry specifications and governmental regulations.
SCOPE
1.1 This test method is a standard procedure for the determination of total aromatic, monoaromatic and diaromatic content in aviation turbine fuels using gas chromatography and vacuum ultraviolet detection (GC-VUV).  
1.2 Concentrations of compound classes and certain individual compounds are determined by percent mass or percent volume.  
1.2.1 This test method is developed for testing aviation turbine engine fuels having concentration test results ranging from 0.487 % to 27.876 % by volume total aromatic compounds, 0.49 % to 27.537 % by volume monoaromatics and 0.027 % to 2.523 % by volume diaromatics.
Note 1: Samples with a final boiling point greater than 300 °C that contain triaromatics and higher polyaromatic compounds are not determined by this test method.  
1.3 Individual hydrocarbon components are not reported by this test method, however, any individual component determinations are included in the appropriate summation of the total aromatic, monoaromatic or diaromatic groups.  
1.3.1 Individual compound peaks are typically not baseline-separated by the procedure described in this test method, that is, some components will coelute. The coelutions are resolved at the detector using VUV absorbance spectra and deconvolution algorithms.  
1.4 This test method has been tested for aviation turbine engine fuels including synthetic alternative jet fuels. This test method may apply to other hydrocarbon streams boiling between hexane (68 °C) and heneicosane (356 °C), but has not been extensively tested for such applications.  
1.5 Units—The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Knowledge of the concentration of benzene may be required for regulatory use, control of gasoline blending, and/or process optimizations.
SCOPE
1.1 This test method covers the quantitation in liquid volume percent of benzene and toluene in finished motor and aviation spark ignition fuels by gas chromatography. This test method has two procedures: Procedure A uses capillary column gas chromatography and Procedure B uses packed column gas chromatography. Procedures A and B have separate precisions.  
1.2 The method has been evaluated for benzene using a D6300-compliant Interlaboratory Study (ILS), with the lowest and highest ILS sample concentration means as follows: (1) Procedure A between 0.12 % and 5.2 % by volume and (2) Procedure B between 0.10 % and 5.0 % by volume.  
1.3 The method has been evaluated for toluene using a D6300-compliant Interlaboratory Study (ILS), with the lowest and highest ILS sample concentration means as follows: (1) Procedure A between 0.4 % and 19.7 % by volume, and (2) Procedure B between 2.0 % and 20.0 % by volume.  
1.4 For reporting, the lowest and highest concentration ranges for benzene and toluene for Procedure A of this test method per Practice D6300 see 13.2.  
1.5 For reporting, the lowest and highest concentration ranges for benzene and toluene for Procedure B of this test method per Practice D6300 see 25.2.  
1.6 For benzene by Procedure A, the following oxygenated fuels are included in the working range: (1) ethanol up to 20 % by volume (E20); (2) methanol up to 10 % by volume (M10). Fuels M85 and E85 were excluded.  
1.7 For benzene by Procedure B the following oxygenated fuels are included in the working range: (1) ethanol up to 20 % by volume (E20); (2) methanol up to 10 % by volume (M10). Fuels M85 and E85 were excluded.  
1.8 For toluene by Procedure A the following oxygenated fuels were included in the working range: (1) ethanol up to 20 % by volume (E20); (2) M85 and E85.  
1.9 For toluene by Procedure B the following oxygenated fuels are included in the working range: (1) ethanol up to 20 % by volume (E20); (2) M85 and E85.  
1.10 Procedure A uses MIBK as the internal standard. Procedure B uses sec-butanol as the internal standard. The use of Procedure B for fuels containing blended butanols requires that sec-butanol be below the detection limit in the fuels as sec-butanol is an internal standard. For Procedure B, an alternative separation column set described in the annex (A2.3, Annex Approach B) uses MEK as the internal standard when butanols may be blended into gasolines.  
1.11 This test method includes a between method bias section for benzene based on Practice D6708 bias assessment between Test Method D3606 Procedure B and Test Method D5769. It is intended to allow Test Method D3606 Procedure B to be used as a possible alternative to Test Method D5769. The Practice D6708 derived benzene correlation equation is applicable for benzene measurements in the reportable range from 0.06 % to 2.76 % by volume as reported by Test Method D3606 Procedure B (see 27.2.1). The correlation complies with EPA’s Performance Based Measurement System (PBMS).  
1.12 Correlation equations are included in the between test methods bias section 14.2.1 of Procedure A to convert Procedure A to the Procedure B volume percent values for benzene and toluene. The correlations are applicable in the concentration ranges of 0.07 % to 5.96 % by volume for benzene and 0.36 % to 20.64 % by volume for toluene as reported by Procedure A.  
1.13 The values stated in SI units are to be regarded as standard. The values given in parentheses are for information only.  
1.14 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use...

SIGNIFICANCE AND USE
5.1 Gas chromatography with sulfur selective detection provides a rapid means to identify and quantify sulfur compounds in various petroleum feeds and products. Often these materials contain varying amounts and types of sulfur compounds. Many sulfur compounds are odorous, corrosive to equipment, and inhibit or destroy catalysts employed in downstream processing. The ability to speciate sulfur compounds in various petroleum liquids is useful in controlling sulfur compounds in finished products and is frequently more important than knowledge of the total sulfur content alone.
SCOPE
1.1 This test method covers the determination of volatile sulfur-containing compounds in light petroleum liquids. This test method is applicable to distillates, gasoline motor fuels (including those containing oxygenates) and other petroleum liquids with a final boiling point of approximately 230 °C (450 °F) or lower at atmospheric pressure. The applicable concentration range will vary to some extent depending on the nature of the sample and the instrumentation used; however, in most cases, the test method is applicable to the determination of individual sulfur species at levels of 0.1 mg/kg to 100 mg/kg.  
1.2 The test method does not purport to identify all individual sulfur components. Detector response to sulfur is linear and essentially equimolar for all sulfur compounds within the scope (1.1) of this test method; thus both unidentified and known individual compounds are determined. However, many sulfur compounds, for example, hydrogen sulfide and mercaptans, are reactive and their concentration in samples may change during sampling and analysis. Coincidently, the total sulfur content of samples is estimated from the sum of the individual compounds determined; however, this test method is not the preferred method for determination of total sulfur.  
1.3 The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units are provided for information only and are not considered standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The composition of the oil included in rubber compounds has a large effect on the characteristics and uses of the compounds. The determination of the saturates, aromatics, and polar compounds is a key analysis of this composition.  
5.2 The determination of the saturates, aromatics, and polar compounds and further analysis of the fractions produced is often used as a research method to aid understanding of oil effects in rubber and other uses.
SCOPE
1.1 This test method covers a procedure for classifying oil samples of initial boiling point of at least 260 °C (500 °F) into the hydrocarbon types of polar compounds, aromatics and saturates, and recovery of representative fractions of these types. This classification is used for specification purposes in rubber extender and processing oils.  
Note 1: See Test Method D2226.  
1.2 This test method is not directly applicable to oils of greater than 0.1 % by mass pentane insolubles. Such oils can be analyzed after removal of these materials, but precision is degraded (see Appendix X1).  
1.3 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. Specific warning statements are given in 6.1, Section 7, A1.4.1, and A1.5.5.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Specification D1655 provides a maximum permissible concentration (5.7 mg/L) of MDA in aviation turbine fuel. This test method will allow the quantification of MDA in aviation turbine fuels. The MDA additive is used for fuel thermal stability control and to reduce fuel degradation caused by the presence of trace metals (copper in particular) in aviation fuels.
SCOPE
1.1 This test method covers the determination of the metal deactivator additive (MDA) content of aviation turbine fuels. The specific MDA determined and used to develop this test method is N,N′-disalicylidene-1,2-propanediamine. Other MDAs have not been tested by this test method.  
1.1.1 This test method specifically covers the determination of uncomplexed MDA content in aviation turbine fuel. MDA is a chelator of divalent metal ions, and the MDA-metal ion complexed species content of aviation turbine fuel will not be accounted for by this test method.  
1.2 This test method is divided into two procedures: (1) Procedure A uses a semi-portable capillary-liquid chromatography system (Capillary-HPLC) that may be used in the field or laboratory; (2) Procedure B uses a standard laboratory version of liquid chromatography (Conventional-HPLC). Procedures A and B have separate precisions.  
1.3 The test method has an interim repeatability determined in accordance with Practice D6300. Based on the mean values of the samples used in the interim repeatability study, Procedure A is applicable in the range of 0.50 mg/mL to 10.0 mg/mL; the range for Procedure B is 0.60 mg/mL to 9.6 mg/mL. Higher concentrations can be determined by dilution, but the precision of the test method has not been determined.  
1.3.1 An extended interlaboratory study (ILS) will be conducted in the future to determine the full repeatability and reproducibility and the final applicable concentration ranges.  
1.3.2 The test method applies to MDA in petroleum-based aviation fuels and Synthetic Aviation Fuels (SAF). However, for the interim precision, a petroleum-based aviation fuel was used. Future ILS will include petroleum-based and SAFs. The test method is applicable to aviation fuels conforming to Specification D1655.  
1.4 Appendix X2 indicates other additives that have been verified to not interfere with the analysis of this test method.  
1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 A knowledge of the hydrocarbon composition of process streams and petroleum products boiling within the range of 160 °C to 343 °C (320 °F to 650 °F) is useful in following the effect of changes in process variables, diagnosing the source of plant upsets, and in evaluating the effect of changes in composition on product performance properties.  
5.2 A test method to determine total cycloparafins and low level aromatic content is necessary to meet specifications for aviation turbine fuel containing synthesized hydrocarbons.
SCOPE
1.1 This test method covers an analytical scheme using the mass spectrometer to determine the hydrocarbon types present in conventional and synthesized hydrocarbons that have a boiling range of 160 °C to 343 °C (320 °F to 650 °F), 5 % to 95 % by volume as determined by Test Method D86. Samples with average carbon number value of paraffins between C12 and C16 and containing paraffins from C10 and C18 can be analyzed. Eleven hydrocarbon types are determined. These include: paraffins, noncondensed cycloparaffins, condensed dicycloparaffins, condensed tricycloparaffins, alkylbenzenes, indans or tetralins, or both, CnH 2n-10 (indenes, etc.), naphthalenes, CnH2n-14  (acenaphthenes, etc.), CnH 2n-16 (acenaphthylenes, etc.), and tricyclic aromatics.  
Note 1: This test method was developed on Consolidated Electrodynamics Corporation Type 103 Mass Spectrometers. Operating parameters for users with a Quadrupole Mass Spectrometer are provided.  
1.2 This test method is intended for use with full boiling range products that contain no significant olefin content.
Biodiesel (FAME components) could interfere with the separation of the sample and the characteristic mass fragments of FAME compounds are not defined in the procedure.
Hydrocarbons containing tertiary carbon fragments, sometimes found in synthetic aviation fuels, will interfere with the characteristic mass fragments of paraffins and result in a false, elevated cycloparaffin content.
Note 2: “No significant olefin content” for this method means D1319.  
1.3 The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units are provided for information only and are not considered standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For a specific warning statement, see 11.1.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The analysis of trace oxygenates in automotive spark-ignition engine fuel has become routine in certain areas to ensure compliance whenever oxygenated fuels are used. In addition, test methods to measure trace levels of oxygenates in automotive spark-ignition fuel are necessary to assess product quality.
SCOPE
1.1 This test method covers the determination of trace oxygenates in automotive spark-ignition engine fuel. The method used is a multidimensional gas chromatographic method using 1,2-dimethoxy ethane as the internal standard. The oxygenates that are analyzed are: methyl-tertiary butyl ether (MTBE), ethyl-tertiary butyl ether (ETBE), diisopropyl ether (DIPE), methanol, tertiary-amyl methyl ether (TAME), n-propanol, i-propanol, n-butanol, i-butanol, tert-butyl alcohol, sec-butyl alcohol, and tert-pentanol. Ethanol is usually not measured as a trace oxygenate since ethanol can be used as the main oxygenate compound in finished automotive spark-ignition fuels such as reformulated automotive spark-ignition fuels. The concentration range of the oxygenates covered in the ILS study was from 10 mg/kg to 2000 mg/kg. In addition this method is also suitable for the measurement of the C5 isomeric alcohols (2-methyl-1-butanol, 2-methyl-2-butanol) present from the fermentation of ethanol.  
1.2 The ethanol blending concentration for which this test method applies ranges from 1 % to 15% by volume. Higher concentrations of ethanol coelute with methanol in the analytical column. Lower levels of ethanol, similar to the other oxygenate, can be calibrated and analyzed also. If higher ethanol concentrations are expected, the window cutting technique can be used to avoid ethanol from entering the analytical column and interfere with the determination of the other oxygenates of interest. Refer to Appendix X1 for details.  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3.1 Alternative units, in common usage, are also provided to increase clarity and aid the users of this test method.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The boiling range distribution of FAMES provides an insight into the composition of product related to the transesterification process. This gas chromatographic determination of boiling range can be used to replace conventional distillation methods for product specification testing with the mutual agreement of interested parties.  
5.2 Biodiesel (FAMES) exhibits a boiling point rather than a distillation curve. The fatty acid chains in the raw oils and fats from which biodiesel is produced are mainly comprised of straight chain hydrocarbons with 16 to 18 carbons that have similar boiling temperatures. The atmospheric boiling point of biodiesel generally ranges from 330 °C to 357 °C. The Specification D6751 value of 360 °C max at 90 % off by Test Method D1160 was incorporated as a precaution to ensure the fuel has not been adulterated with high boiling contaminants.
SCOPE
1.1 This test method covers the determination of the boiling range distribution of fatty acid methyl esters (FAME). This test method is applicable to FAMES (biodiesel, B100) having an initial boiling point greater than 100 °C and a final boiling point less than 615 °C at atmospheric pressure as measured by this test method.  
1.2 The test method can also be applicable to blends of diesel and biodiesel (B1 through B100), however precision for these samples types has not been evaluated.  
1.3 The test method is not applicable for analysis of petroleum containing low molecular weight components (for example naphthas, reformates, gasolines, crude oils).  
1.4 Boiling range distributions obtained by this test method are not equivalent to results from low efficiency distillation such as those obtained with Test Method D86 or D1160, especially the initial and final boiling points.  
1.5 This test method uses the principles of simulated distillation methodology. See Test Methods D2887, D6352, and D7213.  
1.6 The values stated in SI units are to be regarded as standard. The values given in parentheses are for information only.  
1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Heat capacities obtained by this method are those at atmospheric pressure. However, because the temperature range is low, the calculated values are similar to saturated liquid heat capacities in the temperature-pressure range required for most engineering design.
SCOPE
1.1 This test method covers the calculation of liquid heat capacity, Btu/lb · °F (kJ/kg · K), at atmospheric pressure, of petroleum fuels for which distillation data may be obtained in accordance with Test Method D86 without reaching a decomposition point prior to obtaining 90 % by volume distilled.  
1.2 This test method is not applicable at temperatures less than 0 °F (−18 °C) and greater than 60 °F (16 °C) above the volumetric average boiling point of the fuel.  
1.3 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not considered standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The boiling range distribution of light and medium petroleum distillate fractions provides an insight into the composition of feed stocks and products related to petroleum refining process, This gas chromatographic determination of boiling range can be used to replace conventional distillation methods for control of refining operations. This test method can be used for product specification testing with the mutual agreement of interested parties.  
5.2 This test method extends the scope of boiling range determination by gas chromatography to include light and medium petroleum distillate fractions beyond the scope of Test Method D2887 (538 °C) and below Test Method D6352 (700 °C).  
5.3 Boiling range distributions obtained by this test method are theoretically equivalent to those obtained by true boiling point (TBP) distillation (see Test Method D2892). They are not equivalent to results from low efficiency distillation such as those obtained with Test Method D86 or D1160.
SCOPE
1.1 This test method covers the determination of the boiling range distribution of petroleum products. This test method is applicable to petroleum distillates having an initial boiling point greater than 100 °C and a final boiling point less than 615 °C at atmospheric pressure as measured by this test method.  
1.2 The test method is not applicable for analysis of petroleum distillates containing low molecular weight components (for example, naphthas, reformates, gasolines, crude oils). Materials containing heterogeneous components (for example, alcohols, ethers, acids or esters) or residue are not to be analyzed by this test method. See Test Methods D7096, D2887, D6352, or D7169.  
1.3 This test method uses the principles of simulated distillation methodology.  
1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Test methods to determine oxygenates, benzene, and the aromatic content of gasoline are necessary to assess product quality and to meet new fuel regulations.  
5.2 This test method can be used for gasolines that contain oxygenates (alcohols and ethers) as additives. It has been determined that the common oxygenates found in finished gasoline do not interfere with the analysis of benzene and other aromatics by this test method.
SCOPE
1.1 This test method covers the quantitative determination of oxygenates: methyl-t-butylether (MTBE), di-isopropyl ether (DIPE), ethyl-t-butylether (ETBE), t-amylmethyl ether (TAME), methanol (MeOH), ethanol (EtOH), 2-propanol (2-PrOH), t-butanol (t-BuOH), 1-propanol (1-PrOH), 2-butanol (2-BuOH), i-butanol (i-BuOH), 1-butanol (1-BuOH); benzene, toluene and C8–C12 aromatics, and total aromatics in finished motor gasoline by gas chromatography/Fourier Transform infrared spectroscopy (GC/FTIR).  
1.2 This test method covers the following concentration ranges: 0.1 % to 20 % by volume per component for ethers and alcohols; 0.1 % to 2 % by volume benzene; 1 % to 15 % by volume for toluene, 10 % to 40 % by volume total (C6–C12) aromatics.  
1.3 The method has not been tested by ASTM for refinery individual hydrocarbon process streams, such as reformates, fluid catalytic cracking naphthas, etc., used in blending of gasolines.  
1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Some glycol/antifreeze dilution of in-service engine oil is normal under typical operating conditions. However, excessive glycol dilution can lead to decreased performance, premature wear, or sudden engine failure. This test method provides a means of quantifying the level of glycol based antifreeze dilution, allowing the user to take necessary action.
SCOPE
1.1 This test method covers the determination of glycol based antifreeze for in-service engine oil by derivative headspace/gas chromatography.  
1.2 Sample is derivatized in-situ directly in a headspace sampling vial prior to vapor phase extraction and injection into a gas chromatograph.  
1.3 The chemistry of the derivatization is unique to the detection of the molecules of ethylene glycol and 1,2-propylene glycol. 1,3-propylene glycol could also be detected but is not used in any known anti-freeze at this time. Other coolant analyses are beyond the scope of this test method.  
1.4 The derivatization process does not affect glycol breakdown products such as glycolate and formate and hence the presence of these compounds in the oil will not be quantified.  
1.5 The test method concentration range is from 50 µg/g to 1000 µg/g. Lower levels are possible by method modifications. Higher levels are possible through sample dilution.  
1.6 Units—The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 ASTM standard gas chromatographic methods for the analysis of petroleum products require calibration of the gas chromatographic system by preparation and analysis of specified reference mixtures. Frequently, minimal information is given in these methods on the practice of calculating calibration or response factors. Test Methods D2268, D2427, D2804, D2998, D3329, D3362, D3465, D3545, and D3695 are examples. The present practice helps to fill this void by providing a detailed reference procedure for calculating response factors, as exemplified by analysis of a standard blend of C6 to C11 n-paraffins using n-C12 as the diluent.  
5.2 In practice, response factors are used to correct peak areas to a common base prior to final calculation of the sample composition. The response factors calculated in this practice are “multipliers” and prior to final calculation of the results the area obtained for each compound in the sample should be multiplied by the response factor determined for that compound.  
5.3 It has been determined that values for response factors will vary with individual installations. This may be caused by variations in instrument design, columns, and experimental techniques. It is necessary that chromatographs be individually calibrated to obtain the most accurate data.
SCOPE
1.1 This practice covers a procedure for calculating gas chromatographic response factors. It is applicable to chromatographic data obtained from a gaseous mixture or from any mixture of compounds that is normally liquid at room temperature and pressure or solids, or both, that will form a solution with liquids. It is not intended to be applied to those compounds that react in the chromatograph or are not quantitatively eluted. Normal C6 through C11  paraffins have been chosen as model compounds for demonstration purposes.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The determination of the boiling point distribution of crude oils and vacuum residues, as well as other petroleum fractions, yields important information for refinery operation. These boiling point distributions provide information as to the potential mass percent yield of products. This test method may provide useful information that can aid in establishing operational conditions in the refinery. Knowledge of the amount of residue produced is important in determining the economics of the refining process.
SCOPE
1.1 This test method covers the determination of the boiling point distribution and cut point intervals of crude oils and residues by using high temperature gas chromatography. The amount of residue (or sample recovery) is determined using an external standard.  
1.2 This test method extends the applicability of simulated distillation to samples that do not elute completely from the chromatographic system. This test method is used to determine the boiling point distribution through a temperature of 720 °C. This temperature corresponds to the elution of n-C100.  
1.3 This test method is used for the determination of boiling point distribution of crude oils. This test method uses capillary columns with thin films, which results in the incomplete separation of C4-C8 in the presence of large amounts of carbon disulfide, and thus yields an unreliable boiling point distribution corresponding to this elution interval. In addition, quenching of the response of the detector employed to hydrocarbons eluting during carbon disulfide elution, results in unreliable quantitative analysis of the boiling distribution in the C4-C8 region. Since the detector does not quantitatively measure the carbon disulfide, its subtraction from the sample using a solvent-only injection and corrections to this region via quenching factors, results in an approximate determination of the net chromatographic area. A separate, higher resolution gas chromatograph (GC) analysis of the light end portion of the sample may be necessary in order to obtain a more accurate description of the boiling point curve in the interval in question as described in Test Method D7900 (see Appendix X1).  
1.4 This test method is also designed to obtain the boiling point distribution of other incompletely eluting samples such as atmospheric residues, vacuum residues, etc., that are characterized by the fact that the sample components are resolved from the solvent.  
1.5 A correlation between boiling range distribution results from Test Method D2892, and the weight percentage data determined via this method, is presented in Appendix X2.  
1.6 This test method is not applicable for the analysis of materials containing a heterogeneous component such as polyesters and polyolefins.  
1.7 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not considered standard.  
1.8 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. Specific warning statements are given in Section 8.  
1.9 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The determination of WPPO composition is useful in optimization of process variables, diagnosing unit performance, and in evaluating the effect of changes in waste plastic composition on WPPO performance properties.  
5.1.1 Aromatics and olefin hydrocarbon type analysis, including sub-classes, may be useful for evaluating suitability of WPPO as a feedstock for further processing.
SCOPE
1.1 This test method covers a standard procedure for the determination of hydrocarbon types (saturates, olefins, styrenes, aromatics and polyaromatics) of waste plastic process oil (WPPO) from chemical or thermal processes using gas chromatography and vacuum ultraviolet absorption spectroscopy detection (GC-VUV).  
1.1.1 This test method is applicable for plastic recycling and circular schemes including wide range density material from polyethylene and polypropylene.  
1.1.2 The test method is applicable to waste plastic process oil having a final boiling point of 545 °C or lower at atmospheric pressure as measured by this test or Test Method D2887. This test method is limited to samples having a boiling range greater than 36 °C, and having a vapor pressure sufficiently low to permit sampling at ambient temperature.  
1.1.3 WPPOs with initial boiling points less than nC5 (36 °C) and final boiling point less than nC15 (271 °C) may be analyzed by Test Method D8369.  
1.1.4 Appendix X3 is applicable to waste plastic process oils that are predominantly hydrocarbons in the boiling range of pentane, nC5 (36 °C) to tetrahexacontane, nC64 (629 °C).  
1.2 Concentrations of group type totals are determined by percent mass or percent volume. The applicable working ranges are as follows:    
Total Aromatics  
%Mass  
1 to 50  
Monoaromatics  
%Mass  
1 to 50  
Diaromatics  
%Mass  
1 to 15  
Tri-plus aromatics  
%Mass  
0.5 to 5  
PAH  
%Mass  
0.5 to 15  
Saturates  
%Mass  
5 to 99  
Olefins  
%Mass  
1 to 80  
Conjugated diolefins  
%Mass  
0.2 to 5  
Styrenes  
%Mass  
0.2 to 5The final precision concentration ranges will be defined by a future ILS.  
1.2.1 Saturates totals are the result of the summation of normal paraffins, isoparaffins, and naphthenes.  
1.2.2 Aromatics are the summation of monoaromatic and polyaromatic group types. Polyaromatic totals are the result of the summation of diaromatic and tri-plus aromatic group types.  
1.2.3 Olefin totals are the result of the sum of mono-olefins, conjugated diolefins, non-conjugated diolefins, and cyclic olefins.  
1.2.4 Styrenes totals are the sum of styrene and alkylated styrenes. Styrenes are classified separately, neither as aromatic nor olefin.  
1.3 Waste plastic process oil containing mixed plastic types such as polyethylene terephthalate PET and polyvinyl chloride or other material may yield compounds including hetero-compounds that are not speciated by this test method.  
1.4 Individual components are typically not baseline separated by the procedure described in this test method. The coelutions are resolved at the detector using VUV absorbance spectra and deconvolution algorithms.  
1.5 This test method may apply to other process oils from sources such as tires and bio-mass boiling between pentane (36 °C) and tetratetracontane (545 °C), but has not been extensively tested for such applications.  
1.6 Units—The values stated in SI units are to be regarded as standard. No other units of measurement, other than the boiling point of normal paraffins (°F) in Table 2 and Table X.3.1, are included in this standard.  
1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.8 This international standard was developed in accordance with internationally recognized pri...

SIGNIFICANCE AND USE
5.1 The boiling range distribution of petroleum fractions provides an insight into the composition of feedstocks and products related to petroleum refining processes. The gas chromatographic simulation of this determination can be used to replace conventional distillation methods for control of refining operations. This test method can be used for product specification testing with the mutual agreement of interested parties.  
5.2 Boiling range distributions obtained by this test method are essentially equivalent to those obtained by true boiling point (TBP) distillation (see Test Method D2892). They are not equivalent to results from low efficiency distillations such as those obtained with Test Method D86 or D1160.  
5.3 Procedure B was tested with biodiesel mixtures and reports the Boiling Point Distribution of FAME esters of vegetable and animal origin mixed with ultra low sulfur diesel.
SCOPE
1.1 This test method covers the determination of the boiling range distribution of petroleum products. The test method is applicable to petroleum products and fractions having a final boiling point of 538 °C (1000 °F) or lower at atmospheric pressure as measured by this test method. This test method is limited to samples having a boiling range greater than 55.5 °C (100 °F), and having a vapor pressure sufficiently low to permit sampling at ambient temperature.
Note 1: Since a boiling range is the difference between two temperatures, only the constant of 1.8 °F/°C is used in the conversion of the temperature range from one system of units to another.  
1.1.1 Procedure A (Sections 6 – 14)—Allows a larger selection of columns and analysis conditions such as packed and capillary columns as well as a Thermal Conductivity Detector in addition to the Flame Ionization Detector. Analysis times range from 14 min to 60 min.  
1.1.2 Procedure B (Sections 15 – 23)—Is restricted to only 3 capillary columns and requires no sample dilution. In addition, Procedure B is used not only for the sample types described in Procedure A but also for the analysis of samples containing biodiesel mixtures B5, B10, and B20. The analysis time, when using Procedure B (Accelerated D2887), is reduced to about 8 min.  
1.2 This test method is not to be used for the analysis of gasoline samples or gasoline components. These types of samples must be analyzed by Test Method D7096.  
1.3 The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units are provided for information only and are not considered standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The aniline point (or mixed aniline point) is useful as an aid in the characterization of pure hydrocarbons and in the analysis of hydrocarbon mixtures. Aromatic hydrocarbons exhibit the lowest, and paraffins the highest values. Cycloparaffins and olefins exhibit values that lie between those for paraffins and aromatics. In homologous series the aniline points increase with increasing molecular weight. Although it occasionally is used in combination with other physical properties in correlative methods for hydrocarbon analysis, the aniline point is most often used to provide an estimate of the aromatic hydrocarbon content of mixtures.
SCOPE
1.1 These test methods cover the determination of the aniline point of petroleum products and hydrocarbon solvents. Test Method A is suitable for transparent samples with an initial boiling point above room temperature and where the aniline point is below the bubble point and above the solidification point of the aniline-sample mixture. Test Method B, a thin-film method, is suitable for samples too dark for testing by Test Method A. Test Methods C and D are for samples that may vaporize appreciably at the aniline point. Test Method D is particularly suitable where only small quantities of sample are available. Test Method E describes a procedure using an automatic apparatus suitable for the range covered by Test Methods A and B.  
1.2 These test methods also cover the determination of the mixed aniline point of petroleum products and hydrocarbon solvents having aniline points below the temperature at which aniline will crystallize from the aniline-sample mixture.  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4 WARNING—Mercury has been designated by many regulatory agencies as a hazardous substance that can cause serious medical issues. Mercury, or its vapor, has been demonstrated to be hazardous to health and corrosive to materials. Use caution when handling mercury and mercury-containing products. See the applicable product Safety Data Sheet (SDS) for additional information. The potential exists that selling mercury or mercury-containing products, or both, is prohibited by local or national law. Users must determine legality of sales in their location.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. Specific warning statements are given in Section 7.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The absorbance of liquids and the absorptivity of liquid and solids at specified wavelengths in the ultraviolet are useful in characterizing petroleum products.
SCOPE
1.1 This test method covers the measurement of the ultraviolet absorption of a variety of petroleum products. It covers the absorbance of liquids or the absorptivity of liquids and solids, or both, at wavelengths in the region from 220 nm to 400 nm of the spectrum.  
1.2 The use of this test method implies that the conditions of measurement—wavelength, solvent (if any), sample path length, and sample concentration—are specified by reference to one of the examples of the application of this test method in the annexes or by a statement of other conditions of measurement.  
1.3 Examples of the application of this test method are the absorptivity of refined petroleum wax, and the absorptivity of USP petrolatum.  
1.4 The values stated in SI units are to be regarded as the standard. The values stated in Fahrenheit, feet, and inches, indicated in parentheses, are for information only.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For specific warning statements, see 7.3.1, 7.3.3, and 13.4.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The determination of compound types by mass spectrometry requires, in some instances, a preliminary separation of the petroleum sample into representative aromatics and nonaromatics fractions, as in Test Methods D2425, D2786, and D3239. This test method provides a suitable separation technique for this application.
SCOPE
1.1 This test method covers the separation and determination of representative aromatics and nonaromatics fractions from hydrocarbon mixtures that boil between 232 °C and 538 °C (450 °F and 1000 °F). Alternative procedures are provided for the separation of 2 g or 10 g of hydrocarbon mixture.  
Note 1: Some components may not be eluted from the chromatographic column for some types of samples under the conditions used in this method.
Note 2: Test Method D2007 is an alternative method of separating high-boiling oils into polar compounds, aromatics, and saturates fractions.  
1.2 An alternative procedure is provided to handle samples boiling below 232 °C (450 °F), but whose 5 % point is above 178 °C (350 °F) as determined by Test Method D2887. This procedure is given in Appendix X1.  
1.3 The values stated in acceptable SI units are to be regarded as the standard. The values given in parentheses are provided for information purposes only.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 A knowledge of the composition of hydrocarbon refinery streams is useful for process control and quality assurance.  
5.2 Aromatics in gasoline are soon to be limited by federal mandate. This test method can be used to provide such information.
SCOPE
1.1 This test method covers the determination of paraffins, naphthenes, and aromatics by carbon number in low olefinic hydrocarbon streams having final boiling points of 200 °C or less. Hydrocarbons with boiling points greater than 200 °C and less than 270 °C are reported as a single group. Olefins, if present, are hydrogenated and the resultant saturates are included in the paraffin and naphthene distribution. Aromatics boiling at C9 and above are reported as a single aromatic group.  
1.2 This test method is not intended to determine individual components except for benzene and toluene that are the only C6 and C7 aromatics, respectively, and cyclopentane that is the only C5 naphthene. The lower limit of detection for a single hydrocarbon component or group is 0.05 % by mass.  
1.3 This test method is applicable to hydrocarbon mixtures including virgin, catalytically converted, thermally converted, alkylated and blended naphtha.  
1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4.1 The abbreviation for SI unit “coulomb” is “C”.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  Specific precautionary statements are given in Section 8 and Table 1.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Knowledge of the boiling point distribution of stabilized crude oils is important for the marketing, scheduling, and processing of crude oil in the petroleum industry. Test Method D7169 and IP 545 purport to give such a distribution in crude oils, but are susceptible to significant errors in the light ends portion of the distribution as well as in the mass recovery of the whole crude oil due to the interference imposed by the diluent solvent. This test method allows for more accurate determination of the front end of the boiling point distribution curve, in addition to providing important C1 to C9 (nonane) component level information, and more accurate mass recovery at C9 (nonane).
SCOPE
1.1 This test method specifies a method to determine the boiling range distribution of hydrocarbons in stabilized crude oil up to and including n-nonane. A stabilized crude oil is defined as having a Reid Vapor Pressure equivalent to or less than 82.7 kPa. The results of this test method can be combined with those from Test Method D7169 and IP 545 to give a full boiling point distribution of a crude oil (see Appendix X3).  
1.2 The values stated in SI units are to be regarded as the standard. The values given in parentheses are provided for information purposes only.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method for naphthalene hydrocarbons is one of a group of tests used to assess the combustion characteristics of aviation turbine fuels of the kerosene boiling range. The naphthalene hydrocarbon content is determined because naphthalenes, when burned, tend to have a relatively larger contribution to a sooty flame, smoke, and thermal radiation than single ring aromatics.
SCOPE
1.1 This test method covers the determination, by ultraviolet spectrophotometry, of the total concentration of naphthalene, acenaphthene, and alkylated derivatives of these hydrocarbons in jet fuels. This test method is designed to analyze fuels containing not more than 5 % of such components and having end points below 315 °C (600 °F). The range of concentrations used in the interlaboratory test programs which established the precision statements for this test method was 0.08 % to 5.6 % by volume. This test method determines the maximum amount of naphthalenes that could be present.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For specific warning statements, see 8.1 and 8.2.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The carbon distribution and ring content serve to express the gross composition of the heavier fractions of petroleum. These data can be used as an adjunct to the bulk properties in monitoring the manufacture of lubricating oil base stocks by distillation, solvent refining or hydrogenation, or both, and in comparing the composition of stocks from different crude sources. Furthermore, the data can often be correlated with critical product performance properties.
SCOPE
1.1 This test method covers the calculation of the carbon distribution and ring content (Note 1) of olefin-free petroleum oils from measurements of refractive index, density, and molecular weight (n-d-M).2 This test method should not be applied to oils whose compositions are outside the following ranges:  
1.1.1 In terms of carbon distribution—up to 75 % carbon atoms in ring structure; percentage in aromatic rings not larger than 1.5 times the percentage in naphthenic rings.  
1.1.2 In terms of ring content—up to four rings per molecule with not more than half of them aromatic. A correction must be applied for oils containing significant quantities of sulfur.  
Note 1: The composition of complex petroleum fractions is often expressed in terms of the proportions of aromatic rings (RA), naphthene rings (RN), and paraffin chains (CP) that would comprise a hypothetical mean molecule. Alternatively, the composition may be expressed in terms of a carbon distribution, that is, the percentage of the total number of carbon atoms that are present in aromatic ring structures (% CA), naphthene ring structures (% CN), and paraffin chains (% Cp).  
1.2 The values stated in SI units are to be regarded as the standard.  
1.2.1 Exception—The values in parentheses are for information only.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method determines methane (nC1) to hexane (nC6), cut point carbon fraction intervals to nC24 and recovery (nC24+) of live crude oils and condensates without depressurizing, thereby avoiding the loss of highly volatile components and maintaining sample integrity. This test method provides a highly resolved light end profile which can aid in determining and improving appropriate safety measures and product custody transport procedures. Decisions in regards to marketing, scheduling, and processing of crude oils may rely on light end compositional results.  
5.2 Equation of state calculations can be applied to variables provided by this method to allow for additional sample characterization.
SCOPE
1.1 This test method covers the determination of light hydrocarbons and cut point intervals by gas chromatography in live crude oils and condensates with VPCR4 (see Note 1) up to 500 kPa at 37.8 °C.
Note 1: As described in Test Method D6377.  
1.2 Methane (C1) to hexane (nC6) and benzene are speciated and quantitated. Samples containing mass fractions of up to 0.5 % methane, 2.0 % ethane, 10 % propane, or 15 % isobutane may be analyzed. A mass fraction with a lower limit of 0.001 % exists for these compounds.  
1.3 This test method may be used for the determination of cut point carbon fraction intervals (see 3.2.1) of live crude oils and condensates from initial boiling point (IBP) to 391 °C (nC24). The nC24 plus fraction is reported.  
1.4 Dead oils or condensates sampled in accordance with 12.1 may also be analyzed.  
1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.5.1 Exception—Where there is no direct SI equivalent such as tubing size.  
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Knowledge of the individual component composition (speciation) of gasoline fuels and blending stocks is useful for refinery quality control and product specification. Process control and product specification compliance for many individual hydrocarbons can be determined through the use of this test method.  
5.2 This test method is adopted from earlier development and enhancement.4,5,6,7 The chromatographic operating conditions and column tuning process, included in this test method, were developed to provide and enhance the separation and subsequent determination of many individual components not obtained with previous single-column analyses. The column temperature program profile is selected to afford the maximum resolution of possible co-eluting components, especially where these are of two different compound types (for example, a paraffin and a naphthene).  
5.3 Although a majority of the individual hydrocarbons present in petroleum distillates are determined, some co-elution of compounds is encountered. If this test method is utilized to determine bulk hydrocarbon group-type composition (PONA), the user of such data should be cautioned that some error will be encountered due to co-elution and a lack of identification of all components present. Samples containing significant amounts of olefinic or naphthenic, or both, constituents above octane may reflect significant errors in PONA-type groupings.  
5.4 If water is or is suspected of being present, its concentration is determined by the use of Test Method D1744. Other compounds containing oxygen, sulfur, nitrogen, and so forth may also be present, and may co-elute with the hydrocarbons. When known co-elution exists, these are noted in the test method data tables. If determination of these specific compounds is required, it is recommended that test methods for these specific materials be used, such as Test Method D4815 and D5599 for oxygenates, Test Method D5580 for aromatics, and Test Method D5623 for sul...
SCOPE
1.1 This test method covers the determination of individual hydrocarbon components of spark-ignition engine fuels and their mixtures containing oxygenate blends (MTBE, ETBE, ethanol, and so forth) with boiling ranges up to 225 °C. Other light liquid hydrocarbon mixtures typically encountered in petroleum refining operations, such as blending stocks (naphthas, reformates, alkylates, and so forth) may also be analyzed; however, statistical data was obtained only with blended spark-ignition engine fuels.  
1.2 Based on the cooperative study results, individual component concentrations and precision are determined in the range from 0.01 % to approximately 30 % by mass. The test method may be applicable to higher and lower concentrations for the individual components; however, the user must verify the accuracy if the test method is used for components with concentrations outside the specified ranges.  
1.3 This test method also determines methanol, ethanol, t-butanol, methyl t-butyl ether (MTBE), ethyl t-butyl ether (ETBE), and t-amyl methyl ether (TAME) in spark ignition engine fuels in the concentration range from 1 % to 30 % by mass. However, the cooperative study data provided insufficient statistical data for obtaining a precision statement for these compounds.  
1.4 Although a majority of the individual hydrocarbons present are determined, some co-elution of compounds is encountered. If this test method is utilized to estimate bulk hydrocarbon group-type composition (PONA), the user of such data should be cautioned that some error will be encountered due to co-elution and a lack of identification of all components present. Samples containing significant amounts of naphthenic (for example, virgin naphthas) constituents above n-octane may reflect significant errors in PONA-type groupings. Based on the gasoline samples in the interlaboratory cooperative study, this test method is applicable to samples containing less th...

SIGNIFICANCE AND USE
5.1 This test method is intended for use as a guide in cases in which an experimental determination of hydrogen content is not available. Table 1 shows a summary for the range of each variable used in developing the correlation. The mean value and its distribution about the mean, namely the standard deviation, is shown. This indicates, for example, that the mean density for all fuels used in developing the correlation was 783.5 kg/m3  and that two thirds of the samples had a density between 733.2 kg/m3 and 841.3 kg/m3, that is, plus and minus one standard deviation. The correlation is most accurate when the values of the variables to be used in the equation are within one standard deviation of the mean, but is useful up to two standard deviations of the mean. The use of this correlation may be applicable to other hydrocarbon distillates similar to aviation fuels, but only limited data on nonaviation fuels were included in the correlation.  
5.2 Hydrogen content is required to correct gross heat of combustion to net heat of combustion. Net heat is used in aircraft calculation because all combustion products are in the gaseous state, but experimental methods measure gross heat.
SCOPE
1.1 This test method covers the estimation of the hydrogen content (mass percent) of aviation gasolines and aircraft turbine and jet engine fuels.  
1.2 This test method is empirical and is applicable to liquid hydrocarbon fuels that conform to the requirements of specifications for aviation gasolines or aircraft turbine and jet engine fuels of types Jet A, Jet A-1, Jet B, JP-4, JP-5, JP-7, and JP-8.  
Note 1: The procedure for the experimental determination of hydrogen in petroleum fractions is described in Test Methods D1018, D3701, D5291, and D7171.
Note 2: The estimation of the hydrogen content of a hydrocarbon fuel is justifiable only when the fuel belongs to a well-defined class for which a relationship among the hydrogen content and the distillation range, density, and aromatic content has been derived from accurate experimental measurements on representative samples of that class. Even in this case, the possibility that the estimates may be in error by large amounts for individual fuels should be recognized. The fuels used to establish the correlation presented in this test method are defined by the following specifications:    
Fuel  
Specification  
Aviation gasolines  
D910  
Aircraft turbine and jet engine fuels  
JP-4 and JP-5  
MIL-DTL-5624  
JP-7  
MIL-DTL-38219  
JP-8  
MIL-DTL-83133  
Jet A and Jet A-1  
D1655  
Miscellaneous hydrocarbons  
No. 2 Diesel fuel  
Kerosene distillates (similar to Jet A)  
Miscellaneous (includes thinners, gasoline fractions, and unidentified blends)  
Special production fuels (commercial products of nearly pure hydrocarbons
and special high-temperature fuels (HTF) produced for Air Force tests.  
Pure hydrocarbons  
1.3 The values stated in SI units are to be regarded as the standard.  
1.3.1 Exception—The values given in parentheses are for information only.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 For the middle distillates whose boiling range is between 170 °C and 400 °C by such distillation methods like Test Method D2887, Procedure A can separate and determine the content of total aromatics and total nonaromatics by SPE and GC analysis of the resulting fractions. The determination of the total content of saturates and aromatics in petroleum middle distillates is useful to investigate the effects of petroleum processes on production of various finished fuels.  
5.2 The total aromatics content and polycyclic aromatics content are important to characterize the quality of diesel fuels. This test method is demonstrated to be time-saving and eco-friendly by reducing the amount of reagent consumption and avoiding the necessity of solvent evaporation step as required, for example, in such Test Method D2549.  
5.3 The determination of detailed hydrocarbon composition by mass spectrometry requires a preliminary separation of the sample into representative aromatics and nonaromatics, as in Test Method D2425, where Test Method D2549 is used to separate the distillate fuel. The SPE fractionation procedure described herein may provide a suitable fractionation alternative approach for these mass spectrometric types of methods.  
5.4 Biodiesel is a blendstock commodity primarily used as a value-added blending component with diesel fuel. Procedure B can provide a separation and determination technique to monitor the FAME content for FAME biodiesel blends.
SCOPE
1.1 This test method covers the separation and determination of representative aromatics, nonaromatics, and fatty acid methyl ester (FAME) fractions in middle distillates that boil between 170 °C and 400 °C, including biodiesel blends with up to 20 % by volume of FAME, by solid phase extraction and gas chromatography.  
1.2 This test method provides two procedures, A and B. Procedure A is applicable to the petroleum-based middle distillates fuel, and Procedure B is applicable to the biodiesel blends with up to 20 % by volume of FAME.  
1.3 This test method is applicable to middle distillates samples with aromatics content ranging from 5 % to 50 % by mass and biodiesel blends with FAME content in the range of 0.5 % to 20 % by volume. This test method may apply to concentrations outside these ranges, but the precision has not been determined.  
1.4 For Procedure B, biodiesels in the form of fatty acid ethyl ester (FAEE) can also fully elute into the FAME fraction, and they have the similar FID (flame ionization detector) relative response factors with that of FAME. The determined content of FAME fractions are the sum of concentrations of FAME and FAEE by this test method (see 3.2.5).  
1.5 From the investigation results obtained for FAME determination, the low concentrations of monoglycerides (usually less than 0.5 % by mass in biodiesel blends) are not detectable under the gas chromatographic (GC) condition of this test method and will not interfere with the determination of FAME by Procedure B. As a result, biodiesel blends, conforming to the requirements of Specification D7467, containing up to 20 % by volume of biodiesel blendstock meeting the requirements in Specification D6751, typically contain concentrations of monoglycerides of less than 0.1 % by mass. The diglycerides and triglycerides, if present, are not detected under the GC condition of this test method due to their higher boiling points.
Note 1: If a sample is suspected of containing an abnormal FAME biodiesel feedstock than specified in Specification D6751, for example, a sample contaminated with vegetable oil with a high level of total triglycerides, the content of mono-, di-, or tri-glycerides in the isolated FAME fraction may be determined using Test Method D6584. Samples containing biodiesels with a high amount of glycerides than specified in Specification D6751 may contaminate the GC column and not recommended for this test method.  
1.6 The values stated in a...

SIGNIFICANCE AND USE
5.1 This practice covers a series of methods offered to aid users in calibrating U-tube density meters to provide a measure of density and an associated expanded uncertainty. The reference density, as obtained from either an equation of state (EOS) or CRM has an uncertainty that arises from the uncertainty of the measurements of temperature, pressure, and also the chemical purity of the substance studied (origin) or for that matter of the certified reference material. This uncertainty results in an additional uncertainty for the density of these samples. Because the measurements made with U-tube density meters are not absolute, the uncertainty with which the instrument calibration is determined is directly related to the uncertainty of the density obtained.
SCOPE
1.1 This practice outlines procedures for the calibration of U-tube density cells. It is applicable to instruments capable of determining fluid density at temperatures in the range –10 °C to 200 °C and pressures from just greater than the saturation pressure to 140 MPa. The practice refers to density cells as they are utilized to make measurements of fluids primarily in the compressed-liquid state. Examples of substances for which the density can be determined with a calibrated U-tube density meter include: crude oils, gasoline and gasoline-oxygenate blends, diesel and jet fuels, hydraulic fluids, and lubricating oils.  
1.2 This practice specifies a procedure for the determination of the expanded uncertainty of the density measurement.  
1.3 This practice pertains to fluids with viscosities  
1.4 4 The values listed in SI units are regarded as the standard, unless otherwise stated. The SI unit for mass density is kilograms per cubic metre (kg·m-3) and can be given as grams per cubic centimetre (g·cm-3).  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
4.1 The flash point temperature is one measure of the tendency of the test specimen to form a flammable mixture with air under controlled laboratory conditions. It is only one of a number of properties that must be considered in assessing the overall flammability hazard of a material.  
4.2 Flash point is used in shipping and safety regulations to define flammable and combustible materials. Consult the particular regulation involved for precise definitions of these classifications.  
4.3 Flash point can indicate the possible presence of highly volatile and flammable materials in a relatively non-volatile or non-flammable material.  
4.4 In cases where Test Method D2887 data are available, that is, for determination of boiling range distribution or calculation of other physical properties, this test method provides a calculation method for flash point without performing an additional analysis. Table 1 shows the ranges for the IBP, 5 %, and 10 % results for each equation.  
4.5 In the case where the flash point of a fuel has been initially established, the calculated flash point is useful as a flash point check on subsequent samples of that fuel, provided its source and mode of manufacture remain unchanged.
SCOPE
1.1 This test method covers the calculated flash point formula, which represents a means for directly estimating the flash point temperature of distillate fuels from Test Method D2887 data. The value computed from the equation is termed the “calculated flash point.” The calculated flash point formula is applicable to diesel fuel samples based on a correlation to Test Method D93 over the range from 47 °C to 99 °C, and to jet fuel samples based on a correlation to Test Method D56 and Test Method D3828 over the range from 35 °C to 67 °C.  
1.2 The calculated flash point formula is valid for diesel and jet fuels with an IBP between 90 °C and 162 °C (194 °F and 324 °F), Test Method D2887 5 % recovery temperature between 136 °C and 207 °C (277 °F and 405 °F), and Test Method D2887 10 % recovery temperature between 142 °C and 222 °C (288 °F and 432 °F). For each flash point test method (Test Method D56, Test Method D93, and Test Method D3828) a separate equation has been established. See 4.4 for a detailed overview of the simulated distillation IBP, 5 %, and 10 % ranges per equation.  
1.3 A calculated diagnostic parameter, not exceeding a given threshold value, is a prerequisite for acceptance of the calculated flash point.  
1.4 The diagnostic parameter MSPEX (Mean Summed Prediction Error) checks the sample compliance, based on reconstruction of TIBP, T5 %, and T10 % of the sample, via a calculation procedure. A value for MSPEX not exceeding the threshold level of 1.9 °C is a prerequisite for accepting the calculated flash point, CFP.
Note 1: It is important to note that calculated flash point results, at this time, are not recognized by regulatory organizations in verifying conformance to applicable regulations.
Note 2: The calculated flash point derived from simulated distillation data depends upon the accuracy of determination of the IBP temperature and the 5 % and 10 % recovery temperatures.
Note 3: If the user's specification requires a defined flash point test method other than this test method, neither this test method nor any other test method should be substituted for the prescribed test method without obtaining comparative data and an agreement from the specifier.  
1.5 The values stated in SI units are to be regarded as the standard.  
1.5.1 Exception—The values given in parentheses are for information only.  
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.7 This international standard was developed in acc...

SIGNIFICANCE AND USE
5.1 The determination of group type composition of diesel fuel is useful for evaluating quality and expected performance. Aromatics and polyaromatics, in particular, are related to combustion characteristics, cetane number, energy content, lubricity, water solubility and exhaust emissions.  
5.1.1 Aromatic hydrocarbon type analysis may be useful for evaluating refinery processes.  
5.1.2 The ability to determine aromatics content in the presence of FAME may be useful to users of diesel fuel.
SCOPE
1.1 This test method covers a standard procedure for the determination of group type totals of aromatic, polyaromatic, and FAME content in diesel fuel using gas chromatography and vacuum ultraviolet absorption spectroscopy detection (GC-VUV).  
1.1.1 Polyaromatic totals are the result of the summation of diaromatic and tri-plus aromatic group types. Aromatics are the summation of monoaromatic and polyaromatic group types. FAME content is the result of summation of individual fatty acid methyl esters.  
1.1.2 This test method is applicable for renewable diesel fuels from hydrotreated vegetable oil (HVO) or animal fat, gas to liquid (GTL) diesel, light cycle oil, wide boiling range aromatic solvents and biodiesel blends.  
1.2 Concentrations of group type totals are determined by percent mass or percent volume. The applicable working ranges are as follows:    
Total Aromatics %Volume  
0.088 to 77.000  
Total Aromatics %Mass  
0.104 to 79.451    
MonoAromatics %Mass  
0.076 to 67.848    
Diaromatics %Mass  
0.027 to 34.812    
Tri-plus aromatics %Mass  
0.45 to 6.77    
PAH %Mass  
0.028 to 41.586    
FAME %Volume  
1.08 to 21.67  
1.3 Diesel fuel containing biodiesel, (FAME, that is, fatty acid methyl esters including soy methyl esters, rapeseed methylesters, tallow methylesters and canola methylesters) can be analyzed by this test method. The FAME component completely elutes from the analytical column independent of feedstock.  
1.4 Individual hydrocarbon components are not reported by this test method; however, any individual component determinations are included in the appropriate summation of the totals of aromatic, polyaromatic, monoaromatic, diaromatic, tri-plus aromatic, or FAME groups.  
1.4.1 Individual components are typically not baseline-separated by the procedure described in this test method. The coelutions are resolved at the detector using VUV absorbance spectra and deconvolution algorithms.  
1.5 This test method may apply to other hydrocarbon streams boiling between heptane (98 °C) and triacontane (450 °C), but has not been extensively tested for such applications.  
1.6 Units—The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method provides accurate biobased/biogenic carbon content results to materials whose carbon source was directly in equilibrium with CO2 in the atmosphere at the time of cessation of respiration or metabolism, such as the harvesting of a crop or grass living in a field. Special considerations are needed to apply the testing method to materials originating from within artificial environments with non-natural levels of 14C or if the biofeed was grown over the course of several years such as trees and contains “bomb-carbon.” Application of these test methods to materials derived from CO2 uptake within artificial environments is beyond the present scope of this standard.  
5.2 This method uses LSC techniques to quantify the biobased content of a liquid hydrocarbon fuels using sample carbon that has been unmodified. It is designed to be able to incorporate into a refinery laboratory to support biofeed and petroleum coprocessing or blending operations to determine the biocarbon content of the intermediate or finished products. The test results can then be used for optimizing internal parameters or reporting to regulatory agencies.  
5.3 The use of this method requires that a pure petroleum-based sample can be generated that has a similar matrix to each product or stream to be analyzed. For example, gasoline and diesel have very different matrices and will likely require the use of different background measurements for each. Refer to 10.2 for how to determine if the same background sample can be used for more than one product/stream.
SCOPE
1.1 This test method covers quantitatively determining biocarbon content of liquid hydrocarbon fuels with a focus on those produced in a typical petroleum refinery using liquid scintillation counting (LSC). The method is designed to generate analogous results as Test Method D6866 Method C, for low quench samples, without the need of benzene synthesis. The purpose is to be able to use the produced data to report biocarbon content of refinery products to regulatory agencies and monitor refinery operation. The method does not address regulatory reporting or fuel performance.  
1.2 The method is needed to support refinery operations when bio-feeds are co-processed with petroleum within a reactor with a focus on samples with 100 % biocarbon or less (not for 14C labeled species). It allows refineries to report the biocarbon content of refinery products to regulatory agencies such as the Environmental Protection Agency (EPA) or California Air Resources Board (CARB) to comply with regulatory statutes such as The Renewable Fuel Standard (RFS) or Low Carbon Fuel Standard (LCFS).  
1.3 This test method is applicable to any liquid fuel product, petroleum based (pure hydrocarbon), biobased (such as renewable diesel or those that can contain oxygenates such as ethanol), or blends, that contain 1 % to 100 % by mass biocarbon where an instrument background can be experimentally determined using a sample of similar matrix that contains no measurable carbon-14.  
1.4 This test method makes no attempt to teach the basic principles of the instrumentation used although minimum requirements for instrument selection are referenced in Refs (1-11).2 However, the preparation of samples for the above test methods is described. No details of instrument operation are included here. These are best obtained from the manufacturer of the specific instrument in use.  
1.5 Pre-Requisite Requirements For Method Execution—This test method uses artificial carbon-14 (14C) within the method. Great care shall be taken to prevent laboratory contamination of the elevated 14C. Once in the laboratory, artificial 14C can contaminate a variety of laboratory surfaces that can lead to artificially high sample biocarbon measurements. If vigorous cleaning attempts to remove the artificial 14C from a laboratory are unsuccessful, instrumentation and sample preparation may have to be moved to a ne...

SIGNIFICANCE AND USE
5.1 Density is a fundamental physical property that may be used in conjunction with other properties to characterize the quality of crude oils.  
5.2 The density or relative density of crude oils is used for the conversion of measured volumes to volumes at the standard temperatures of 15 °C or 60 °F and for the conversion of crude mass measurements into volume units.  
5.3 The application of the density result obtained from this test method, for fiscal or custody transfer accounting calculations, may require measurements of the water and sediment contents obtained on similar specimens of the crude oil parcel.
SCOPE
1.1 This test method covers the determination of the density, relative density, and API gravity of crude oils that may be handled in a normal fashion as liquids at test temperatures between 15 °C and 35 °C utilizing either manual or automated sample injection equipment. This test method applies to crude oils with high vapor pressures provided appropriate precautions are taken to prevent vapor loss during transfer of the sample to the density analyzer.  
1.2 This test method was evaluated in interlaboratory study testing using crude oils in the 0.75 g/mL to 0.95 g/mL range. Lighter crude oil may require special handling to prevent vapor losses.  
1.3 The values stated in SI units are to be regarded as standard. Other units of measurement are included in this standard. The accepted units of measurement of density are grams per millilitre and kilograms per cubic metre.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. Specific warning statements are given in 7.4, 7.5, and 7.6.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Test methods to determine benzene and the aromatic content of gasoline are necessary to assess product quality and to meet fuel regulations.  
5.2 This test method can be used for gasolines that contain oxygenates (alcohols and ethers) as additives. It has been determined that the common oxygenates found in finished gasoline do not interfere with the analysis of benzene and other aromatics by this test method.
SCOPE
1.1 This test method covers the determination in volume percent of benzene, toluene, other specified individual aromatic compounds, and total aromatics in finished motor gasoline, including gasolines containing oxygenated blending components, by gas chromatography/mass spectrometry (GC/MS). Precision is calculated for benzene, toluene and total aromatics.  
1.2 This test method has been evaluated using a D6300-compliant Interlaboratory Study (ILS), with the lowest and highest ILS sample averages listed as follows: benzene, 0.09 % to 4.00 %; toluene, 1.0 % to 13.0 %; and total (C6 to C12) aromatics, 10.0 % to 42.0 %. The ILS study did not test the method for individual hydrocarbon process streams produced in a refinery, such as reformates, fluid catalytic cracked naphthas, and so forth, used in the blending of gasolines.  
1.3 Results are reported to the nearest 0.01 % for benzene and 0.1 % for the other aromatics by liquid volume. The Report Section (14) describes the applicable reporting ranges of this test method.  
1.4 This test method includes a between test method bias section for spark-ignition engine fuel benzene reporting based on Practice D6708 assessment between Test Method D5769 and Test Method D3606 as a possible Test Method D5769 alternative to Test Method D3606. The Practice D6708 derived correlation equation is only applicable for blended fuels with benzene results concentration range from 0.05 % to 2.50 % by volume as measured and reported by Test Method D5769.  
1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to its use.  
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Biodiesel is a blendstock commodity primarily used as a value-added blending component with diesel fuel.  
5.2 This test method is applicable for quality control in the production and distribution of diesel fuel and biodiesel blends containing FAME.
SCOPE
1.1 This test method covers the determination of the content of fatty acid methyl esters (FAME) biodiesel in diesel fuel oils. It is applicable to concentrations from 1.00 % to 20 % by volume (see Note 1). This procedure is applicable only to FAME. Biodiesel in the form of fatty acid ethyl esters (FAEE) will cause a negative bias.
Note 1: Using the proper ATR sample accessory, the range may be expanded from 1 % to 100 % by volume, however precision data is not available above 20 % by volume.  
1.2 The values stated in SI units of measurement are to be regarded as the standard. The values given in parentheses are for information only.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Density is a fundamental physical property that can be used in conjunction with other properties to characterize both the light and heavy fractions of petroleum and petroleum products.  
5.2 Determination of the density or relative density of petroleum and its products is necessary for the conversion of measured volumes to volumes at the standard temperature of 15 °C.
SCOPE
1.1 This test method covers the determination of the density, relative density, and API Gravity of petroleum distillates and viscous oils that can be handled in a normal fashion as liquids at the temperature of test, utilizing either manual or automated sample injection equipment. Its application is restricted to liquids with total vapor pressures (see Test Method D5191) typically below 100 kPa and viscosities (see Test Method D445 or D7042) typically below about 15 000 mm2/s at the temperature of test. The total vapor pressure limitation however can be extended to >100 kPa provided that it is first ascertained that no bubbles form in the U-tube, which can affect the density determination. Some examples of products that may be tested by this procedure include: gasoline and gasoline-oxygenate blends, diesel, jet, basestocks, waxes, and lubricating oils.  
1.1.1 Waxes and highly viscous samples were not included in the 1999 interlaboratory study (ILS) sample set that was used to determine the current precision statements of the method, since all samples evaluated at the time were analyzed at a test temperature of 15 °C. Wax and highly viscous samples require a temperature cell operated at elevated temperatures necessary to ensure a liquid test specimen is introduced for analysis. Consult instrument manufacturer instructions for appropriate guidance and precautions when attempting to analyze wax or highly viscous samples. Refer to the Precision and Bias section of the method and Note 9 for more detailed information about the 1999 ILS that was conducted.  
1.2 In cases of dispute, the referee method is the one where samples are introduced manually as in 6.2 or 6.3, as appropriate for sample type.  
1.3 When testing opaque samples, and when not using equipment that is capable of automatic bubble detection, proper procedure shall be established so that the absence of air bubbles in the U-tube can be established with certainty. For the determination of density in crude oil samples use Test Method D5002.  
1.4 The values stated in SI units are regarded as the standard, unless stated otherwise. The accepted units of measure for density are grams per millilitre (g/mL) or kilograms per cubic metre (kg/m3).  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For specific warning statements, see 3.2.1, Section 7, 9.1, 10.2, and Appendix X1.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Benzene is a compound that endangers health, and the concentration is limited by environmental protection agencies to produce a less toxic gasoline.  
5.2 This test method is fast, simple to run, and inexpensive.  
5.3 This test method is applicable for quality control in the production and distribution of spark-ignition engine fuels.
SCOPE
1.1 This test method covers the determination of the percentage of benzene in spark-ignition engine fuels. It is applicable to concentrations from 0.1 % to 5 % by volume.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The aromatic hydrocarbon content of motor diesel fuels is a factor that can affect their cetane number and exhaust emissions.  
5.2 The United States Environmental Protection Agency (USEPA) regulates the aromatic content of diesel fuels. California Air Resources Board (CARB) regulations place limits on the total aromatics content and polynuclear aromatic hydrocarbon content of motor diesel fuel, thus requiring an appropriate analytical determination to ensure compliance with the regulations. Producers of diesel fuels will require similar determinations for process and quality control. This test method can be used to make such determinations.  
5.3 This test method is applicable to materials in the boiling range of motor diesel fuels and is unaffected by fuel coloration. Test Method D1319, which has been mandated by the USEPA for the determination of aromatics in motor diesel fuel, excludes materials with final boiling points greater than 315 °C (600 °F) from its scope. Test Method D2425 is applicable to the determination of both total aromatics and polynuclear aromatic hydrocarbons in diesel fuel, but is much more costly and time consuming to perform.  
5.4 Results obtained by this test method have been shown to be statistically more precise than those obtained from Test Method D1319 for typical diesel fuels, and this test method has a shorter analysis time.3 Results from this test method for total polynuclear aromatic hydrocarbons are also expected to be at least as precise as those of Test Method D2425.
SCOPE
1.1 This test method covers the determination of the total amounts of monoaromatic and polynuclear aromatic hydrocarbon compounds in motor diesel fuels and blend stocks by supercritical fluid chromatography (SFC). The range of aromatics concentration to which this test method is applicable is from 1 % to 75 % by mass. The range of polynuclear aromatic hydrocarbon concentrations to which this test method is applicable is from 0.5 % to 50 % by mass.  
1.2 This test method includes relative bias for Test Method D5186 versus Test Method D1319 and Test Method D6591 versus Test Method D5186 for diesel fuels. The applicable ranges of the correlation ranges are presented in the Relative Bias section. The correlations are applicable only in the stated ranges and only to diesel fuels.  
1.3 This test method and correlations were developed for diesel samples not containing biodiesel; the presence of biodiesel will interfere with the results. The correlation equations are only applicable between these concentration ranges and to diesel fuels that do not contain biodiesel.  
1.4 The values stated in SI units are to be regarded as standard. The values stated in inch-pound units are for information only.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Accurate quantitative compositional information on hydrocarbon types can be useful in determining the effects of processes in the production of various finished fuels. Producers may require additional determinations such as n-paraffins, i-paraffins, naphthenes, and aromatics for process optimization. This information also may be useful for indicating the quality of fuels and for assessing the relative combustion properties of finished fuels. This test method can be used to make such determinations.
SCOPE
1.1 This test method covers the quantitative determination of total n-paraffins, total i-paraffins, total naphthenes (cycloparaffins), total one ring (1R) and total two ring plus (2R+) aromatic hydrocarbons in hydrocarbon liquids having a boiling point between 36 °C and 343 °C by GCxGC (flow modulated comprehensive two-dimensional gas chromatography). The method has been applied to aviation turbine fuels and is applicable to other low olefinic fuels in the stated boiling point range.  
1.2 This test method has an interim precision. An expanded full interlaboratory study is to be completed in    
Hydrocarbon Type  
Lower limit
(mass percent)  
Upper limit
(mass percent)  
Total i-paraffins  
22.0  
24.3  
Total n-paraffins  
19.0  
21.9  
Total naphthenes (cycloparaffins)  
34.3  
36.7  
Total one ring aromatics  
18.7  
21.8  
Total two ring plus aromatics  
0.5  
1.9  
1.3 This test method is applicable to other group type concentration ranges, to other hydrocarbon types such as selected individual components, for example, benzene, toluene, or n-paraffins by carbon number, or to other hydrocarbon streams; however, precision has not been determined at this time. A future ILS will include a variety of sample types and extend the reporting.  
1.4 This test method is not intended to determine unsaturated hydrocarbons, such as olefins, content which may interfere with the cycloparaffins; this test method is applicable to samples with D1319.  
1.5 This test method is not intended to determine FAME (fatty acid methyl esters). For such applications, Test Method D7797, IP 585, or equivalent test methods are available.  
1.6 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.7 This standard test method does not mandate or describe a specific software package for data processing and display. Any commercially available GCxGC software used for data processing and display shall meet the requirements for the calculation of the results. Appendix X1 provides some guidelines.  
1.8 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.9 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 In gasoline blending, the determination of organic oxygenated compounds is important. Alcohols, ethers, and other oxygenates are added to gasoline to increase the octane number and to reduce tailpipe emissions of carbon monoxide. They must be added in the proper concentration and ratios to meet regulatory limitations and to avoid phase separation and problems with engine performance or efficiency.  
5.2 This test method provides sufficient oxygen-to-hydro-carbon selectivity and sensitivity to allow determination of oxygenates in gasoline samples without interference from the bulk hydrocarbon matrix.
SCOPE
1.1 This test method covers a gas chromatographic procedure for the quantitative determination of organic oxygenated compounds in gasoline having a final boiling point not greater than 220 °C and oxygenates having a boiling point limit of 130 °C. It is applicable when oxygenates are present in the 0.1 % to 20 % by mass range.  
1.2 This test method is intended to determine the mass concentration of each oxygenate compound  present in a gasoline. This requires knowledge of the identity of each oxygenate being determined (for calibration purposes). However, the oxygen-selective detector used in this test method exhibits a response that is proportional to the mass of oxygen. It is, therefore, possible to determine the mass concentration of oxygen contributed by any oxygenate compound in the sample, whether or not it is identified. Total oxygen content in a gasoline may be determined from the summation of the accurately determined individual oxygenated compounds. The summed area of other, uncalibrated or unknown oxygenated compounds present, may be converted to a mass concentration of oxygen and summed with the oxygen concentration of the known oxygenated compounds.  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Ethers, alcohols, and other oxygenates can be added to gasoline to increase octane number and to reduce emissions. Type and concentration of various oxygenates are specified and regulated to ensure acceptable commercial gasoline quality. Drivability, vapor pressure, phase separation, exhaust, and evaporative emissions are some of the concerns associated with oxygenated fuels.  
5.2 This test method is applicable to both quality control in the production of gasoline and for the determination of deliberate or extraneous oxygenate additions or contamination.
SCOPE
1.1 This test method covers the determination of ethers and alcohols in gasolines by gas chromatography. Specific compounds determined are methyl tert-butylether (MTBE), ethyl tert-butylether (ETBE), tert-amylmethylether (TAME), diisopropylether (DIPE), methanol, ethanol, isopropanol, n-propanol, isobutanol, tert-butanol, sec-butanol, n-butanol, and tert-pentanol (tert-amylalcohol).  
1.2 Individual ethers are determined from 0.20 % to 20.0 % by mass. Individual alcohols are determined from 0.20 % to 12.0 % by mass. Equations used to convert to mass percent oxygen and to volume percent of individual compounds are provided. At concentrations 10 % by volume olefins, the interference may be >0.20 % by mass. Annex A1 gives a chromatogram showing the interference observed with a gasoline containing 10 % by volume olefins.  
1.3 This test method includes a relative bias correlation for ethanol in spark-ignition engine fuels for the U.S. EPA regulations reporting based on Practice D6708 accuracy assessment between Test Method D4815 and Test Method D5599 as a possible Test Method D4815 alternative to Test Method D5599. The Practice D6708 derived correlation equation is only applicable for ethanol in fuels in the concentration range from 2.28 % to 14.42 % by mass as measured by Test Method D4815. The applicable Test Method D5599 range for ethanol is from 2.16 % to 14.39 % by mass as reported by Test Method D5599.  
1.4 Alcohol-based fuels, such as M-85 and E-85, MTBE product, ethanol product, and denatured alcohol, are specifically excluded from this test method. The methanol content of M-85 fuel is considered beyond the operating range of the system.  
1.5 Benzene, while detected, cannot be quantified using this test method and shall be analyzed by alternate methodology (see Test Method D3606).  
1.6 The values stated in SI units are to be regarded as standard. Alternate units, in common usage, are also provided to increase clarity and aid the users of this test method.  
1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The quantitative determination of olefins in spark-ignition engine fuels is required to comply with government regulations.  
5.2 Knowledge of the total olefin content provides a means to monitor the efficiency of catalytic cracking processes.  
5.3 This test method provides better precision for olefin content than Test Method D1319. It also provides data in a much shorter time, approximately 20 min following calibration, and maximizes automation to reduce operator labor.  
5.4 This test method is not applicable to M85 or E85 fuels, which contain 85 % methanol and ethanol, respectively.
SCOPE
1.1 This test method provides for the quantitative determination of total olefins in the C4 to C10 range in spark-ignition engine fuels or related hydrocarbon streams, such as naphthas and cracked naphthas. Olefin concentrations in the range from 0.2 % by liquid-volume or mass to 5.0 % by liquid-volume or mass, or both, can be determined directly on the as-received sample whereas olefins in samples containing higher concentrations are determined after appropriate sample dilution prior to analysis.  
1.2 This test method is applicable to samples containing alcohols and ethers; however, samples containing greater than 15 % alcohol must be diluted. Samples containing greater than 5.0 % ether must also be diluted to the 5.0 % or less level, prior to analysis. When ethyl-tert-butylether is present, only olefins in the C4 to C9 range can be determined.  
1.3 This test method can not be used to determine individual olefin components.  
1.4 This test method can not be used to determine olefins having higher carbon numbers than C10.
Note 1: Precision was determined only on samples containing MTBE and ethanol.  
1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 A knowledge of the hydrocarbon components comprising a petroleum naphtha, reformate, or alkylate is useful in valuation of crude oils, in alkylation and reforming process control, in product quality assessment, and for regulatory purposes. Detailed hydrocarbon composition is also used as input in the mathematical modeling of refinery processes.  
5.2 Separation of naphtha components by the procedure described in this test method can result in some peaks that represent coeluting compounds. This test method cannot attribute relative concentrations to the coelutants. In the absence of supporting information, use of the results of this test method for purposes which require such attribution is not recommended.
SCOPE
1.1 This detailed hydrocarbon analysis (DHA) test method covers the determination of hydrocarbon components paraffins, naphthenes, and monoaromatics (PNA) of petroleum naphthas as enumerated in Table 1. Components eluting after n-nonane (bp 150.8 °C) are determined as a single group.  
1.2 This test method is applicable to olefin-free (D1319 or D6839. The hydrocarbon mixture must have a 98 % point of 250 °C or less as determined by Test Method D3710 or D7096 or equivalent.  
1.3 Components that are present at the 0.05 % by mass level or greater can be determined.  
1.4 This test method may not be completely accurate for PNA above carbon number C7; Test Method D5443 or D6839 may be used to verify or complement the results of this test method for carbon numbers >C7.  
1.5 Detailed hydrocarbon components in olefin containing samples may be determined by DHA Test Methods D6729, D6730, or D6733.  
1.6 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. Specific warning statements are given in Section 8.  
1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The presence of impurities in ETBE product can have a deleterious effect upon the value of ETBE as a fuel additive. Oxygenate and olefin contents are of primary concern. This test method provides a knowledge of the composition of ETBE product. This is useful in the evaluation of process operations control, in the valuation of the product, and for regulatory purposes.
SCOPE
1.1 This test method covers the determination of the purity of ethyl tert-butyl ether (ETBE) by gas chromatography. It also provides a procedure to measure impurities in ETBE such as C4 to C12 olefins, methyl, isopropyl and tert-butyl alcohols, methyl sec-butyl and methyl tert-amyl ethers, acetone, and methyl ethyl ketone.  
1.2 This test method is not applicable to the determination of ETBE in gasoline.  
1.3 Water cannot be determined by this test method and shall be measured by a procedure such as Test Method D6304 and the result used to normalize the chromatographic values.  
1.4 Most of the impurities in ETBE are resolved by the test method, however, some co-elution is encountered.  
1.5 This test method is inappropriate for impurities that boil at temperatures higher than 180 °C or for impurities that cause poor or no response in a flame ionization detector, such as water.  
1.6 The values stated in SI units of measurement are preferred and used throughout the standard. Alternate units, in common usage, are also provided to improve clarity and aid the user of this test method.  
1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method provides sufficient PCB data for many regulatory requirements. While the most common regulatory level is 50 ppm (dry weight corrected), lower limits are used in some locations. Since sensitivities will vary for different types of samples, one shall demonstrate a sufficient method detection limit for the matrix of interest.  
5.2 This test method differs from Test Method D4059 in that it provides for more sample clean-up options, utilizes a capillary column for better pattern recognition and interference discrimination, and includes both a qualitative screening and a quantitative results option.
SCOPE
1.1 This test method2 covers a two-tiered analytical approach to PCB screening and quantitation of liquid and solid wastes, such as oils, sludges, aqueous solutions, and other waste matrices.  
1.2 Tier I is designed to screen samples rapidly for the presence of PCBs.  
1.3 Tier II is used to determine the concentration of PCBs, typically in the range of from 2 mg/kg to 50 mg/kg. PCB concentrations greater than 50 mg/kg are determined through analysis of sample dilutions.  
1.4 This is a pattern recognition approach, which does not take into account individual congeners that might occur, such as in reaction by-products. This test method describes the use of Aroclors3 1016, 1221, 1232, 1242, 1248, 1254, 1260, 1262, and 1268, as reference standards, but others could also be included. Aroclors 1016 and 1242 have similar capillary gas chromatography (GC) patterns. Interferences or weathering are especially problematic with Aroclors 1016, 1232, and 1242 and may make distinction between the three difficult.  
1.5 This test method provides sample clean up and instrumental conditions necessary for the determination of Aroclors. Gas chromatography (GC) using capillary column separation technique and electron capture detector (ECD) are described. Other detectors, such as atomic emission detector (AED) and mass spectrometry (MS), may be used if sufficient performance (for example, sensitivity) is demonstrated. Further details about the use of GC and ECD are provided in Practices E355, E697, and E1510.  
1.6 Quantitative results are reported on the dry weights of waste samples.  
1.7 Quantification limits will vary depending on the type of waste stream being analyzed.  
1.8 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.9 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.10 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Free and bonded glycerin content reflects the quality of biodiesel. A high content of free glycerin may cause problems during storage, or in the fuel system, due to separation of the glycerin. A high total glycerin content can lead to injector fouling and may also contribute to the formation of deposits at injection nozzles, pistons, and valves.
SCOPE
1.1 This test method covers the quantitative determination of total monoglyceride, total diglyceride, total triglyceride, and free and total glycerin in B-100 methyl esters by gas chromatography. The range of quantitation for monoglyceride is 0.009 % to 0.77860 % by mass, for diglyceride is 0.092353 % to 0.54475 % by mass, and for triglyceride is 0.00092857 % to 1.3881 % by mass. The range of quantitation for free glycerin is 0.0005714 % to 0.019533 % by mass and for total glycerin from 0.0090714 % to 0.42767 % by mass. This procedure is not applicable to vegetable oil methyl esters obtained from lauric oils, such as coconut oil and palm kernel oil.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method is used for specification analysis of high-purity n-heptane and  isooctane, which are used as ASTM Knock Test Reference Fuels. Hydrocarbon impurities or contaminants, which can adversely affect the octane number of these fuels, are precisely determined by this method.
SCOPE
1.1 This test method covers and provides for the analysis of high-purity (greater than 99.5 % by volume) n-heptane and isooctane (2,2,4-trimethylpentane), which are used as primary reference standards in determining the octane number of a fuel. Individual compounds present in concentrations of less than 0.01 % can be detected. Columns specified by this test method may not allow separation of all impurities in reference fuels.  
1.2 The values stated in SI units are to be regarded as the standard.  
1.2.1 Exception—The values given in parentheses are for information only.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Leakage of aqueous engine coolant into the crank case weakens the ability of the oil to lubricate. If ethylene glycol is present, it promotes varnish and deposit formation. This test method is designed for early detection to prevent coolant from accumulating and seriously damaging the engine.
SCOPE
1.1 This test method covers the determination of ethylene glycol as a contaminant in used engine oil. This test method is designed to quantitate ethylene glycol in the range from 5 mass ppm to 200 mass ppm.  
1.2 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For specific warning statements, see Section 7.  
Note 1: A qualitative determination of glycol-base antifreeze is provided in Test Methods D2982. Procedure A is sensitive to about 100 ppm.  
1.3 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The presence of impurities in MTBE product can have a deleterious effect upon the value of MTBE as a gasoline additive. Oxygenate and olefin contents are of primary concern. This test method provides a knowledge of the composition of MTBE product. This is useful in the evaluation of process operations control, in the valuation of the product, and for regulatory purposes.  
5.2 Open tubular column gas chromatography with a flame ionization detector, used by the test method, is a technique that is sensitive to the contaminants commonly found in MTBE, and a technique that is widely used.
SCOPE
1.1 This test method covers the determination of the purity of methyl tert-butyl ether (MTBE) by gas chromatography. It also provides a procedure to measure impurities in MTBE such as C4 to C12 olefins, methyl, isopropyl and tert-butyl alcohols, methyl sec-butyl and methyl tert-amyl ethers, acetone, and methyl ethyl ketone. Impurities are determined to a minimum concentration of 0.02 % by mass.  
1.2 This test method is not applicable to the determination of MTBE in gasoline.  
1.3 Water cannot be determined by this test method and must be measured by a procedure such as Test Method D1364 and the result used to normalize the chromatographic values.  
1.4 A majority of the impurities in MTBE is resolved by the test method, however, some co-elution is encountered.  
1.5 This test method is inappropriate for impurities that boil at temperatures higher than 180 °C or for impurities that cause poor or no response in a flame ionization detector, such as water.  
1.6 The values stated in SI (metric) units of measurement are preferred and used throughout the standard.  
1.6.1 Exception—Alternate units, in common usage, are also provided to improve clarity and aid the user of this test method.  
1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Methanol is used in production of crude oil to prevent formation of gas hydrates. The presence of residual methanol in crude oils can lead to costly problems in refinery operations.
SCOPE
1.1 This test method covers the determination of methanol in crude oils by direct injection multidimensional gas chromatography in the concentration range of 15 ppm (m/m) to 900 ppm (m/m). The pooled limit of quantification (PLOQ) is 15 ppm (m/m).  
1.2 This test method is applicable only to crude oils containing less than or equal to 0.1 % (v/v) water.  
1.3 This test method has not been tested with crude oil samples that are solid or waxy, or both, at ambient temperatures.  
1.4 The values stated in SI units are to be regarded as standard. Alternate units, in common usage, are also provided to increase clarity and aid the users of this test method.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.