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ASTM D3120-06

(Test Method)

Standard Test Method for Trace Quantities of Sulfur in Light Liquid Petroleum Hydrocarbons by Oxidative Microcoulometry

Standard Test Method for Trace Quantities of Sulfur in Light Liquid Petroleum Hydrocarbons by Oxidative Microcoulometry

SCOPE
1.1 This test method covers the determination of sulfur concentration in the range from 3.0 to 1000 mg/kg in light liquid hydrocarbons boiling in the range from 26 to 274°C (80 to 525°F).
1.2 Other materials falling within the distillation range specified in 1.1, but having sulfur concentrations above 1000 mg/kg, may be tested using appropriate dilutions to bring them within the specified limit. In addition, sample types that may be outside the specified distillation range, such as diesels and biodiesels, may be analyzed by this test method.
1.3 The values stated in SI units are to be regarded as the standard. The values given in parentheses are provided for information only. The preferred units are milligrams per kilogram (mg/kg).
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 and health practices and determine the applicability of regulatory limitations prior to use. For specific hazard statements, see Sections 7-9.

General Information

Status
Historical
Publication Date
30-Nov-2006
ICS
75.080 - Petroleum products in general
Technical Committee
D02 - Petroleum Products, Liquid Fuels, and Lubricants
Drafting Committee
D02.03 - Elemental Analysis
Current Stage
Ref Project

Relations

Replaces
ASTM D3120-03a - Standard Test Method for Trace Quantities of Sulfur in Light Liquid Petroleum Hydrocarbons by Oxidative Microcoulometry
Effective Date
01-Dec-2006
Replaced By
ASTM D3120-06e1 - Standard Test Method for Trace Quantities of Sulfur in Light Liquid Petroleum Hydrocarbons by Oxidative Microcoulometry
Effective Date
01-Dec-2006
Referred By
ASTM D7578-20 - Standard Guide for Calibration Requirements for Elemental Analysis of Petroleum Products and Lubricants
Effective Date
01-Dec-2006
Referred By
ASTM D8076-21b - Standard Specification for 100 Research Octane Number Test Fuel for Automotive Spark-Ignition Engines
Effective Date
01-Dec-2006
Referred By
ASTM D5623-19 - Standard Test Method for Sulfur Compounds in Light Petroleum Liquids by Gas Chromatography and Sulfur Selective Detection
Effective Date
01-Dec-2006
Referred By
ASTM D8011-19 - Standard Specification for Natural Gasoline as a Blendstock in Ethanol Fuel Blends or as a Denaturant for Fuel Ethanol
Effective Date
01-Dec-2006
Referred By
ASTM D8291-23 - Standard Test Method for Evaluation of Performance of Automotive Engine Oils in the Mitigation of Low-Speed, Preignition in the Sequence IX Gasoline Turbocharged Direct-Injection, Spark-Ignition Engine
Effective Date
01-Dec-2006
Referred By
ASTM D7807-20 - Standard Test Method for Determination of Boiling Range Distribution of Hydrocarbon and Sulfur Components of Petroleum Distillates by Gas Chromatography and Chemiluminescence Detection
Effective Date
01-Dec-2006
Referred By
ASTM D7467-20a - Standard Specification for Diesel Fuel Oil, Biodiesel Blend (B6 to B20)
Effective Date
01-Dec-2006
Referred By
ASTM D7862-21 - Standard Specification for Butanol for Blending with Gasoline for Use as Automotive Spark-Ignition Engine Fuel
Effective Date
01-Dec-2006
Referred By
ASTM D4806-21a - Standard Specification for Denatured Fuel Ethanol for Blending with Gasolines for Use as Automotive Spark-Ignition Engine Fuel
Effective Date
01-Dec-2006
Referred By
ASTM D7455-19 - Standard Practice for Sample Preparation of Petroleum and Lubricant Products for Elemental Analysis
Effective Date
01-Dec-2006
Referred By
ASTM D6227-18(2023) - Standard Specification for Unleaded Aviation Gasoline Containing a Non-hydrocarbon Component
Effective Date
01-Dec-2006
Referred By
ASTM D7155-20 - Standard Practice for Evaluating Compatibility of Mixtures of Turbine Lubricating Oils
Effective Date
01-Dec-2006
Referred By
ASTM D3246-15 - Standard Test Method for Sulfur in Petroleum Gas by Oxidative Microcoulometry
Effective Date
01-Dec-2006

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ASTM D3120-06 - Standard Test Method for Trace Quantities of Sulfur in Light Liquid Petroleum Hydrocarbons by Oxidative MicrocoulometryASTM D3120-06 - Standard Test Method for Trace Quantities of Sulfur in Light Liquid Petroleum Hydrocarbons by Oxidative Microcoulometry
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ASTM D3120-06 - Standard Test Method for Trace Quantities of Sulfur in Light Liquid Petroleum Hydrocarbons by Oxidative Microcoulometry
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Standards Content (Sample)

NOTICE: This standard has either been superseded and replaced by a new version or withdrawn. Contact ASTM
International (www.astm.org) for the latest information.
An American National Standard
Designation:D3120–06
Standard Test Method for
Trace Quantities of Sulfur in Light Liquid Petroleum
1
Hydrocarbons by Oxidative Microcoulometry
This standard is issued under the fixed designation D3120; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision.Anumber in parentheses indicates the year of last reapproval.A
superscript epsilon (e) indicates an editorial change since the last revision or reapproval.
This standard has been approved for use by agencies of the Department of Defense.
1. Scope* D4177 Practice for Automatic Sampling of Petroleum and
Petroleum Products
1.1 This test method covers the determination of sulfur
D6299 Practice forApplying Statistical QualityAssurance
concentration in the range from 3.0 to 1000 mg/kg in light
Techniques to Evaluate Analytical Measurement System
liquid hydrocarbons boiling in the range from 26 to 274°C (80
Performance
to 525°F).
2.2 OSHA Regulations:
1.2 Other materials falling within the distillation range
OSHA Regulations 29 CFR, paragraphs 1910.1000 and
specified in 1.1, but having sulfur concentrations above 1000
3
1910.1200
mg/kg,maybetestedusingappropriatedilutionstobringthem
withinthespecifiedlimit.Inaddition,sampletypesthatmaybe
3. Summary of Test Method
outside the specified distillation range, such as diesels and
3.1 A liquid sample is introduced into a pyrolysis tube
biodiesels, may be analyzed by this test method.
maintained at a temperature between 900-1200°C, having a
1.3 The values stated in SI units are to be regarded as the
flowing stream of gas containing 50-80% oxygen and 20-50%
standard. The values given in parentheses are provided for
inertgas(forexample,argon,helium,etc.)Oxidativepyrolysis
information only. The preferred units are milligrams per
converts the sulfur to sulfur dioxide, which then flows into a
kilogram (mg/kg).
titration cell where it reacts with triiodide ion present in the
1.4 This standard does not purport to address all of the
electrolyte. The triiodide ion consumed is coulometrically
safety concerns, if any, associated with its use. It is the
replaced and the total current (I 3 t) required to replace it is a
responsibility of the user of this standard to establish appro-
measure of the sulfur present in the sample.
priate safety and health practices and determine the applica-
3.2 The reaction occurring in the titration cell as sulfur
bility of regulatory limitations prior to use. For specific hazard
dioxide enters is:
statements, see Sections 7-9.
2 2 1
I 1SO 1H O→SO 13I 12H (1)
3 2 2 3
2. Referenced Documents
The triiodide ion consumed in the above reaction is gener-
2
2.1 ASTM Standards:
ated coulometrically thus:
D1193 Specification for Reagent Water
2 2 2
3I →I 12e (2)
D1298 TestMethodforDensity,RelativeDensity(Specific
3
Gravity), or API Gravity of Crude Petroleum and Liquid
3.3 These microequivalents of triiodide ion (iodine) are
Petroleum Products by Hydrometer Method
equal to the number of microequivalents of titratable SO ion
2
D4052 Test Method for Density and Relative Density of
entering the titration cell.
Liquids by Digital Density Meter
4. Significance and Use
D4057 Practice for Manual Sampling of Petroleum and
Petroleum Products
4.1 This test method is used to determine the concentration
ofsulfurinlightliquidhydrocarbons,gasoline,anddieselsand
their additives, where such concentrations of sulfur can be
1
This test method is under the jurisdiction of ASTM Committee D02 on
detrimental to their production, performance, and use. The
PetroleumProductsandLubricantsandisthedirectresponsibilityofSubcommittee
D02.03 on Elemental Analysis.
measurement of sulfur in the production and final product of
Current edition approved Dec. 1, 2006. Published January 2007. Originally
gasolineanddieselisrequiredforbothregulatorypurposesand
approved in 1972. Last previous edition approved in 2003 as D3120–03a.
2
For referenced ASTM standards, visit the ASTM website, www.astm.org, or
contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM
3
Standards volume information, refer to the standard’s Document Summary page on Available from U.S. Government Printing Office, Superintendent of Docu-
the ASTM website. ments, 732 N. Capitol St., NW, Mail Stop: SDE, Washington, DC 20401.
*A Summary of Changes section appears at the end of this standard.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.
1

---------------------- Page: 1 ----------------------
NOTICE: This standard has either been superseded and replaced by a new version or withdrawn. Contact ASTM
International (www.astm.org) for the latest information.
D3120–06
NOTE 1—Take care not to use excessive stirring and possibly da
...

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1.1 This test method covers the determination of solvent extractables in petroleum waxes.  
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1.1 This test method covers the determination of the color of refined oils such as undyed motor and aviation gasoline, jet propulsion fuels, naphthas and kerosine, and, in addition, petroleum waxes and pharmaceutical white oils.  
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1.3 The values stated in inch-pound units or in SI units and which are not in parentheses are to be regarded as the standard. The values given in parentheses are for information only.  
Note 2: Oil tubes and apparatus used in this test method have traditionally been marked in inches, (the tube is required to be etched with 1/8 in. divisions.) The Saybolt Color Numbers are aligned with inch, 1/2 in., 1/4 in., and 1/8 in. changes in the depth of oil. These fractional inch changes do not readily correspond to SI equivalents and in view of the preponderance of apparatus already in use and marked in inches, the inch/pound unit is regarded as the standard. However the test method does use SI units of length when the length is not directly related to divisions on the oil tube and Saybolt Color Numbers. The test method uses SI units for temperature.  
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Standard Practice for Calculating Viscosity of a Blend of Petroleum Products

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5.1 Predicting the viscosity of a blend of components is a common problem. Both the Wright Blending Method and the ASTM Blending Method, described in this practice, may be used to solve this problem.  
5.2 The inverse problem, predicating the required blend fractions of components to meet a specified viscosity at a given temperature may also be solved using either the Inverse Wright Blending Method or the Inverse ASTM Blending Method.  
5.3 The Wright Blending Methods are generally preferred since they have a firmer basis in theory, and are more accurate. The Wright Blending Methods require component viscosities to be known at two temperatures. The ASTM Blending Methods are mathematically simpler and may be used when viscosities are known at a single temperature.  
5.4 Although this practice was developed using kinematic viscosity and volume fraction of each component, the dynamic viscosity or mass fraction, or both, may be used instead with minimal error if the densities of the components do not differ greatly. For fuel blends, it was found that viscosity blending using mass fractions gave more accurate results. For base stock blends, there was no significant difference between mass fraction and volume fraction calculations.  
5.5 The calculations described in this practice have been computerized as a spreadsheet and are available as an adjunct.3
SCOPE
1.1 This practice covers the procedures for calculating the estimated kinematic viscosity of a blend of two or more petroleum products, such as lubricating oil base stocks, fuel components, residual fuel oil with kerosene, crude oils, and related products, from their kinematic viscosities and blend fractions.  
1.2 This practice allows for the estimation of the fraction of each of two petroleum products needed to prepare a blend meeting a specific viscosity.  
1.3 This practice may not be applicable to other types of products, or to materials which exhibit strong non-Newtonian properties, such as viscosity index improvers, additive packages, and products containing particulates.  
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 Logarithms may be either common logarithms or natural logarithms, as long as the same are used consistently. This practice uses common logarithms. If natural logarithms are used, the inverse function, exp(×), must be used in place of the base 10 exponential function, 10×, used herein.  
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ASTM D4952-23(Test Method)
Standard Test Method for Qualitative Analysis for Active Sulfur Species in Fuels and Solvents (Doctor Test)

SIGNIFICANCE AND USE
5.1 Sulfur present as mercaptans or as hydrogen sulfide in distillate fuels and solvents can attack many metallic and non-metallic materials in fuel and other distribution systems. A negative result in the doctor test ensures that the concentration of these compounds is insufficient to cause such problems in normal use.
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1.1 This test method covers and is intended primarily for the detection of mercaptans in motor fuel, kerosine, and similar petroleum products. This method may also provide information on hydrogen sulfide and elemental sulfur that may be present in these sample types.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
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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.

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  • Standard
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    English language
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