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ASTM D6367-04(2008)

(Specification)

Standard Specification for AMS (α-Methylstyrene)

Standard Specification for AMS (<span class='unicode'>&#x03B1;</span>-Methylstyrene)

ABSTRACT
This specification establishes the requirements for AMS (alpha-Methylstyrene). Sampled specimens shall conform to the following physical and chemical properties: minimum AMS content; maximum phenol content; maximum polymer content; inhibitor content; appearance; and color (Pt-Co units).
SCOPE
1.1 This specification covers AMS (α-Methylstyrene).
1.2 The following applies to all limits in this specification: for purposes of determining conformance with this specification, an observed value or a calculated value shall be rounded off “to the nearest unit” in the last right-hand digit used in expressing the specification limit, in accordance with the rounding-off method of Practice E 29.
1.3 Consult current OSHA regulations, suppliers' Material Safety Data Sheets, and local regulations for all materials used in this specification.

General Information

Status
Historical
Publication Date
30-Jun-2008
ICS
75.080 - Petroleum products in general
Technical Committee
D16 - Aromatic, Industrial, Specialty and Related Chemicals
Drafting Committee
D16.07 - Styrene, Ethylbenzene and C9 and C10 Aromatic Hydrocarbons
Current Stage
Ref Project

Relations

Replaces
ASTM D6367-04 - Standard Specification for AMS (alpha-Methylstyrene)
Effective Date
01-Jul-2008
Replaced By
ASTM D6367-12 - Standard Specification for AMS (&#x03b1;-Methylstyrene)
Effective Date
01-Dec-2012
Referred By
ASTM D7977-23 - Standard Test Methods for Polymer Content of AMS (α-Methylstyrene)
Effective Date
01-Jul-2008

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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NOTICE: This standard has either been superseded and replaced by a new version or withdrawn.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
Designation:D6367 −04(Reapproved2008)
StandardSpecification for
AMS (α-Methylstyrene)
This standard is issued under the fixed designation D6367; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (´) indicates an editorial change since the last revision or reapproval.
1. Scope D3160 Test Method for Phenol Content of Cumene (Isopro-
pylbenzene) or AMS (α–Methylstyrene)
1.1 This specification covers AMS (α-Methylstyrene).
D3437 Practice for Sampling and Handling Liquid Cyclic
1.2 The following applies to all limits in this specification:
Products
for purposes of determining conformance with this
D4590 Test Method for Colorimetric Determination of
specification, an observed value or a calculated value shall be
p-tert-Butylcatechol In Styrene Monomer or AMS
rounded off “to the nearest unit” in the last right-hand digit
(α–Methylstyrene) by Spectrophotometry
used in expressing the specification limit, in accordance with
D5386 Test Method for Color of Liquids Using Tristimulus
the rounding-off method of Practice E29.
Colorimetry
D6144 Test Method forAnalysis ofAMS (α-Methylstyrene)
1.3 Consult current OSHA regulations, suppliers’ Material
Safety Data Sheets, and local regulations for all materials used by Capillary Gas Chromatography
E29 Practice for Using Significant Digits in Test Data to
in this specification.
Determine Conformance with Specifications
2. Referenced Documents 2.2 Other Documents:
OSHA Regulations 29 CFR paragraphs 1910.1000 and
2.1 ASTM Standards:
1910.1200
D1209 Test Method for Color of Clear Liquids (Platinum-
Cobalt Scale)
3. Properties
D2121 Test Methods for Polymer Content of Styrene Mono-
3.1 AMS shall conform to the requirements shown in
mer and AMS (α–Methylstyrene)
Table 1.
4. Sampling
This specification is under the jurisdiction of ASTM Committee D16 on
4.1 Sample the material in accordance with Practice D3437.
Aromatic Hydrocarbons and Related Chemicals and is the direct responsibility of
Subcommittee D16.07 on Styrene, Ethylbenzene and C9 and C10 Aromatic
5. Keywords
Hydrocarbons.
Current edition approved July 1, 2008. Published July 2008. Originally approved
5.1 α-Methylstyrene; AMS; catechol; TBC; tertiary-butyl
in 1999. Last previous edition approved in 2004 as D6367 – 04. DOI: 10.1520/
...


This document is not an ASTM standard and is intended only to provide the user of an ASTM standard an indication of what changes have been made to the previous version. Because
it may not be technically possible to adequately depict all changes accurately, ASTM recommends that users consult prior editions as appropriate. In all cases only the current version
of the standard as published by ASTM is to be considered the official document.
Designation:D6367–99 Designation: D 6367 – 04 (Reapproved 2008)
Standard Specification for
AMS (a-Methylstyrene)
This standard is issued under the fixed designation D 6367; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (´) indicates an editorial change since the last revision or reapproval.
1. Scope
1.1 This specification covers AMS (a-Methylstyrene).
1.2 The following applies to all limits in this specification: for purposes of determining conformance with this specification, an
observed value or a calculated value shall be rounded off “to the nearest unit” in the last right-hand digit used in expressing the
specification limit, in accordance with the rounding-off method of Practice E 29.
1.3 Consult current OSHA regulations, suppliers’ Material Safety Data Sheets, and local regulations for all materials used in
this specification.
2. Referenced Documents
2.1 ASTM Standards:
D 1209 Test Method for Color of Clear Liquids (Platinum-Cobalt Scale)
D 2121Test Method for Polymer Content of Styrene Monomer and a-Methylstyrene Test Methods for Polymer Content of
Styrene Monomer and AMS (Methylstyrene)
D 3160 Test Method for Phenol Content of Cumene (Isopropylbenzene) or AMS (a-Meththylstyrene) (Methylstyrene)
D 3437 Practice for Sampling and Handling Liquid Cyclic Products
D 4590 Test Method for Colorimetric Determination of p-tert-Butylcatechol inp-tert-Butylcatechol In Styrene Monomer or
AMS (a-Methylstyrene)(Methylstyrene) by Spectrophotometry
D 5386 Test Method for Color of Liquids Using Tristimulus Colorimetry
D 6144Standard Test Test Method for Analysis of AMS (a-Methylstyrene) by Capillary Gas Chromatography
E 29 Practice for Using Significant Digits in Test Data to Determine Conformance with Specifications
2.2 Other Documents:
OSHA Regulations, 29CFR, paragraphs 1910.1000 and 1910.1200 OSHA Regulations 29CFR paragraphs 1910.1000 and
1910.1200
3. Properties
3.1 AMS shall conform to the requirements shown in
Table 1.
4. Sampling
4.1 Sample the material in accordance with Practice D 3437.
5. Keywords
5.1AMS;a-Methylstyrene
This specification is under the jurisdiction ofASTM Committee D16 onAromatic Hydrocarbons and Related Chemicals and is the direct responsibility of Subcommittee
D16.07 on Styrene, Ethylbenzene, and C and C Aromatic Hydrocarbons.
9 10
Current edition approved Jan. 10, 1999. Published March 1999.
This specification is under the jurisdiction ofASTM Committee D16 on
...

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ASTM D6367-21(Specification)
Standard Specification for AMS (α-Methylstyrene)

ABSTRACT
This specification establishes the requirements for AMS (alpha-Methylstyrene). Sampled specimens shall conform to the following physical and chemical properties: minimum AMS content; maximum phenol content; maximum polymer content; inhibitor content; appearance; and color (Pt-Co units).
SCOPE
1.1 This specification covers AMS (α-Methylstyrene).  
1.2 The following applies to all limits in this specification: for purposes of determining conformance with this specification, an observed value or a calculated value shall be rounded off “to the nearest unit” in the last right-hand digit used in expressing the specification limit, in accordance with the rounding-off method of Practice E29.  
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 Consult current OSHA regulations, suppliers’ Safety Data Sheets, and local regulations for all materials used in this specification.  
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ASTM D6809-20a(Guide)
Standard Guide for Quality Control and Quality Assurance Procedures for Aromatic Hydrocarbons and Related Materials

SIGNIFICANCE AND USE
5.1 Quality Control and Quality Assurance practices are important for the optimum operation of testing laboratories using D16 methods for aromatic hydrocarbons and related materials. Quality procedure guidelines, like those described in this document or other suitably correct QA/QC-related reference, can be useful to optimally perform these methods.
SCOPE
1.1 This guide contains non-mandatory Quality Assurance/Quality Control (QA/QC) activities that may be referenced in standards maintained by ASTM Committee D16 on Aromatic Hydrocarbons and Related Materials.  
1.2 This guide does not purport to address all of the issues that may be pertinent to an active QA/QC process.  
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.

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ASTM D189-24(Test Method)
Standard Test Method for Conradson Carbon Residue of Petroleum Products

SIGNIFICANCE AND USE
5.1 The carbon residue value of burner fuel serves as a rough approximation of the tendency of the fuel to form deposits in vaporizing pot-type and sleeve-type burners. Similarly, provided alkyl nitrates are absent (or if present, provided the test is performed on the base fuel without additive) the carbon residue of diesel fuel correlates approximately with combustion chamber deposits.  
5.2 The carbon residue value of motor oil, while at one time regarded as indicative of the amount of carbonaceous deposits a motor oil would form in the combustion chamber of an engine, is now considered to be of doubtful significance due to the presence of additives in many oils. For example, an ash-forming detergent additive may increase the carbon residue value of an oil yet will generally reduce its tendency to form deposits.  
5.3 The carbon residue value of gas oil is useful as a guide in the manufacture of gas from gas oil, while carbon residue values of crude oil residuums, cylinder and bright stocks, are useful in the manufacture of lubricants.
SCOPE
1.1 This test method covers the determination of the amount of carbon residue (Note 1) left after evaporation and pyrolysis of an oil, and is intended to provide some indication of relative coke-forming propensities. This test method is generally applicable to relatively nonvolatile petroleum products which partially decompose on distillation at atmospheric pressure. Petroleum products containing ash-forming constituents as determined by Test Method D482 or IP Method 4 will have an erroneously high carbon residue, depending upon the amount of ash formed (Note 2 and Note 4).  
Note 1: The term carbon residue is used throughout this test method to designate the carbonaceous residue formed after evaporation and pyrolysis of a petroleum product under the conditions specified in this test method. The residue is not composed entirely of carbon, but is a coke which can be further changed by pyrolysis. The term carbon residue is continued in this test method only in deference to its wide common usage.
Note 2: Values obtained by this test method are not numerically the same as those obtained by Test Method D524. Approximate correlations have been derived (see Fig. X1.1), but need not apply to all materials which can be tested because the carbon residue test is applied to a wide variety of petroleum products.
Note 3: The test results are equivalent to Test Method D4530, (see Fig. X1.2).
Note 4: In diesel fuel, the presence of alkyl nitrates such as amyl nitrate, hexyl nitrate, or octyl nitrate causes a higher residue value than observed in untreated fuel, which can lead to erroneous conclusions as to the coke forming propensity of the fuel. The presence of alkyl nitrate in the fuel can be detected by Test Method D4046.  
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 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.  
1.4 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.  
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ASTM D3326-07(2024)(Practice)
Standard Practice for Preparation of Samples for Identification of Waterborne Oils

SIGNIFICANCE AND USE
4.1 Identification of a recovered oil is determined by comparison with known oils selected because of their possible relationship to the particular recovered oil, for example, suspected or questioned sources. Thus, samples of such known oils must be collected and submitted along with the unknown for analysis. It is unlikely that identification of the sources of an unknown oil by itself can be made without direct matching, that is, solely with a library of analyses.
SCOPE
1.1 This practice covers the preparation for analysis of waterborne oils recovered from water. The identification is based upon the comparison of physical and chemical characteristics of the waterborne oils with oils from suspect sources. These oils may be of petroleum or vegetable/animal origin, or both. Seven procedures are given as follows:    
Sections  
Procedure A (for samples of more than 50 mL volume containing significant quantities of hydrocarbons with boiling points above 280 °C)  
8 to 12  
Procedure B (for samples containing significant quantities of hydrocarbons with boiling points above 280 °C)  
13 to 17  
Procedure C (for waterborne oils containing significant amounts of components boiling below 280 °C and to mixtures of these and higher boiling components)  
18 to 22  
Procedure D (for samples containing both petroleum and vegetable/animal derived oils)  
23 to 27  
Procedure E (for samples of light crudes and medium distillate fuels)  
28 to 34  
Procedure F (for thin films of oil-on-water)  
35 to 39  
Procedure G (for oil-soaked samples)  
40 to 44  
1.2 Procedures for the analytical examination of the waterborne oil samples are described in Practice D3415 and Test Methods D3328, D3414, and D3650. Refer to the individual oil identification test methods for the sample preparation method of choice. The deasphalting effects of the sample preparation method should be considered in selecting the best methods.  
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. Specific caution statements are given in Sections 6 and 32.  
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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ASTM D445-24(Test Method)
Standard Test Method for Kinematic Viscosity of Transparent and Opaque Liquids (and Calculation of Dynamic Viscosity)

SIGNIFICANCE AND USE
5.1 Many petroleum products, and some non-petroleum materials, are used as lubricants, and the correct operation of the equipment depends upon the appropriate viscosity of the liquid being used. In addition, the viscosity of many petroleum fuels is important for the estimation of optimum storage, handling, and operational conditions. Thus, the accurate determination of viscosity is essential to many product specifications.
SCOPE
1.1 This test method specifies a procedure for the determination of the kinematic viscosity, ν, of liquid petroleum products, both transparent and opaque, by measuring the time for a volume of liquid to flow under gravity through a calibrated glass capillary viscometer. The dynamic viscosity, η, can be obtained by multiplying the kinematic viscosity, ν, by the density, ρ, of the liquid.  
Note 1: For the measurement of the kinematic viscosity and viscosity of bitumens, see also Test Methods D2170 and D2171.
Note 2: ISO 3104 corresponds to Test Method D445 – 03.  
1.2 The result obtained from this test method is dependent upon the behavior of the sample and is intended for application to liquids for which primarily the shear stress and shear rates are proportional (Newtonian flow behavior). If, however, the viscosity varies significantly with the rate of shear, different results may be obtained from viscometers of different capillary diameters. The procedure and precision values for residual fuel oils, which under some conditions exhibit non-Newtonian behavior, have been included.  
1.3 The range of kinematic viscosities covered by this test method is from 0.2 mm2/s to 300 000 mm2/s (see Table A1.1) at all temperatures (see 6.3 and 6.4). The precision has only been determined for those materials, kinematic viscosity ranges and temperatures as shown in the footnotes to the precision section.  
1.4 The values stated in SI units are to be regarded as standard. The SI unit used in this test method for kinematic viscosity is mm2/s, and the SI unit used in this test method for dynamic viscosity is mPa·s. For user reference, 1 mm2/s = 10-6 m2/s = 1 cSt and 1 mPa·s = 1 cP = 0.001 Pa·s.  
1.5 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.  
1.6 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.  
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ASTM D3415-98(2024)(Practice)
Standard Practice for Identification of Waterborne Oils

SIGNIFICANCE AND USE
4.1 Oil from one crude oil field is readily distinguishable from another, and differences in the makeup of oils from the same crude oil field can often be observed as well. Refined oils are fractions from crude oil stocks, usually derived from distillation processes. Two refined oils of the same type differ because of dissimilarities in the characteristics of their crude oil feed stocks as well as variations in refinery processes and any subsequent contact with other oils mixed in during transfer operations from residues in tanks, ships, pipes, hoses, and so forth. Thus, all petroleum oils, to some extent, have chemical compositions different from each other.  
4.2 Identification of a recovered oil is determined by comparison with known oils selected because of their possible relationship to the particular recovered oil, for example, suspected sources. Thus, samples of such known oils must be collected and submitted along with the unknown for analysis. Identification of the source of an unknown oil by itself cannot be made without comparison to a known oil. The principles of oil spill identification are discussed in Ref (1).4  
4.3 Many similarities (within uncertainties of sampling, analysis and weathering) will be needed to establish the identity beyond a reasonable doubt. The analyses described will distinguish many, but not all samples. Examples of weathering of various classes of oils are included in Ref (2).  
4.4 This practice is a guide to the use of ASTM test methods for the analysis of oil samples for oil spill identification purposes. The evaluation of results from analytical methods and preparation of an Oil Spill Identification Report are discussed in this practice. Other analytical methods are described in Ref (3).  
4.5 A quality assurance program for oil spill identification is specified.
SCOPE
1.1 This practice covers the broad concepts of sampling and analyzing waterborne oils for identification and comparison with suspected source oils. Detailed procedures are referenced in this practice. A general approach is given to aid the investigator in planning a program to solve the problem of chemical characterization and to determine the source of a waterborne oil sample.  
1.2 This practice is applicable to all waterborne oils taken from water bodies, either natural or man-made, such as open oceans, estuaries or bays, lakes, rivers, smaller streams, canals; or from beaches, marshes, or banks lining or edging these water systems. Generally, the waterborne oils float on the surface of the waters or collect on the land surfaces adjoining the waters, but occasionally these oils, or portions, are emulsified or dissolved in the waters, or are incorporated into the sediments underlying the waters, or into the organisms living in the water or sediments.  
1.3 This practice as presently written proposes the use of specific analytical techniques described in the referenced ASTM standards. As additional techniques for characterizing waterborne oils are developed and written up as test methods, this practice will be revised.  
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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ASTM D6708-24(Practice)
Standard Practice for Statistical Assessment and Improvement of Expected Agreement Between Two Test Methods that Purport to Measure the Same Property of a Material

SIGNIFICANCE AND USE
5.1 This practice can be used to determine if a constant, proportional, or linear bias correction can improve the degree of agreement between two methods that purport to measure the same property of a material.  
5.2 The bias correction developed in this practice can be applied to a single result (X) obtained from one test method (method X) to obtain a predicted result ( Y^) for the other test method (method Y).
Note 5: Users are cautioned to ensure that  Y^ is within the scope of method Y before its use.  
5.3 The between methods reproducibility established by this practice can be used to construct an interval around  Y^ that would contain the result of test method Y, if it were conducted, with approximately 95 % probability.  
5.4 This practice can be used to guide commercial agreements and product disposition decisions involving test methods that have been evaluated relative to each other in accordance with this practice.  
5.5 The magnitude of a statistically detectable bias is directly related to the uncertainties of the statistics from the experimental study. These uncertainties are related to both the size of the data set and the precision of the processes being studied. A large data set, or, highly precise test method(s), or both, can reduce the uncertainties of experimental statistics to the point where the “statistically detectable” bias can become “trivially small,” or be considered of no practical consequence in the intended use of the test method under study. Therefore, users of this practice are advised to determine in advance as to the magnitude of bias correction below which they would consider it to be unnecessary, or, of no practical concern for the intended application prior to execution of this practice.
Note 6: It should be noted that the determination of this minimum bias of no practical concern is not a statistical decision, but rather, a subjective decision that is directly dependent on the application requirements of the users.
SCOPE
1.1 This practice covers statistical methodology for assessing the expected agreement between two different standard test methods that purport to measure the same property of a material, and for the purpose of deciding if a simple linear bias correction can further improve the expected agreement. It is intended for use with results obtained from interlaboratory studies meeting the requirement of Practice D6300 or equivalent (for example, ISO 4259). The interlaboratory studies shall be conducted on at least ten materials in common that among them span the intersecting scopes of the test methods, and results shall be obtained from at least six laboratories using each method. Requirements in this practice shall be met in order for the assessment to be considered suitable for publication in either method, if such publication includes claim to have been carried out in compliance with this practice. Any such publication shall include mandatory information regarding certain details of the assessment outcome as specified in the Report section of this practice.  
1.2 The statistical methodology is based on the premise that a bias correction will not be needed. In the absence of strong statistical evidence that a bias correction would result in better agreement between the two methods, a bias correction is not made. If a bias correction is required, then the parsimony principle is followed whereby a simple correction is to be favored over a more complex one.
Note 1: Failure to adhere to the parsimony principle generally results in models that are over-fitted and do not perform well in practice.  
1.3 The bias corrections of this practice are limited to a constant correction, proportional correction, or a linear (proportional + constant) correction.  
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ASTM D6749-24(Test Method)
Standard Test Method for Pour Point of Petroleum Products (Automatic Air Pressure Method)

SIGNIFICANCE AND USE
5.1 The pour point of a petroleum product is an index of the lowest temperature of its utility for certain applications. Flow characteristics, like pour point, can be critical for the correct operation of lubricating systems, fuel systems, and pipeline operations.  
5.2 Petroleum blending operations require precise measurement of the pour point.  
5.3 Test results from this test method can be determined at either 1 °C or 3 °C intervals.  
5.4 This test method yields a pour point in a format similar to Test Method D97/IP 15 when the 3 °C interval results are reported. However, when specification requires Test Method D97/IP 15, do not substitute this test method.
Note 2: Since some users may wish to report their results in a format similar to Test Method D97/IP 15 (in 3 °C intervals), the precision data were derived for the 3 °C intervals. For statements on bias relative to Test Method D97/IP 15, see 13.3.1.  
5.5 This test method has better repeatability and reproducibility relative to Test Method D97/IP 15 as measured in the 1998 interlaboratory test program (see Section 13).
SCOPE
1.1 This test method covers the determination of pour point of petroleum products by an automatic apparatus that applies a slightly positive air pressure onto the specimen surface while the specimen is being cooled.  
1.2 This test method is designed to cover the range of temperatures from −57 °C to +51 °C; however, the range of temperatures included in the (1998) interlaboratory test program only covered the temperature range from −51 °C to −11 °C.  
1.3 Test results from this test method can be determined at either 1 °C or 3 °C testing intervals.  
1.4 This test method is not intended for use with crude oils.
Note 1: The applicability of this test method on residual fuel samples has not been verified. For further information on the applicability, refer to 13.4.  
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.

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ASTM D1500-24(Test Method)
Standard Test Method for ASTM Color of Petroleum Products (ASTM Color Scale)

SIGNIFICANCE AND USE
4.1 Determination of the color of petroleum products is used mainly for manufacturing control purposes and is an important quality characteristic, since color is readily observed by the user of the product. In some cases, the color may serve as an indication of the degree of refinement of the material. When the color range of a particular product is known, a variation outside the established range may indicate possible contamination with another product. However, color is not always a reliable guide to product quality and should not be used indiscriminately in product specifications.
SCOPE
1.1 This test method covers the visual determination of the color of a wide variety of petroleum products, such as lubricating oils, heating oils, diesel fuel oils, and petroleum waxes.  
Note 1: Test Method D156 is applicable to refined products that have an ASTM color lighter than 0.5.
Note 2: The color of some dyed products may extend outside color range defined by the glass reference standards employed in the testing procedure. Furthermore, samples used to determine the precision and bias did not include dyed products.
Note 3: It is up to the user to determine the suitability of this test method for their dyed products.  
1.2 This test method reports results specific to the test method and recorded as “ASTM Color.”  
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.

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ASTM
ASTM D6300-24(Practice)
Standard Practice for Determination of Precision and Bias Data for Use in Test Methods for Petroleum Products, Liquid Fuels, and Lubricants

SIGNIFICANCE AND USE
5.1 ASTM test methods are frequently intended for use in the manufacture, selling, and buying of materials in accordance with specifications and therefore should provide such precision that when the test is properly performed by a competent operator, the results will be found satisfactory for judging the compliance of the material with the specification. Statements addressing precision and bias are required in ASTM test methods. These then give the user an idea of the precision of the resulting data and its relationship to an accepted reference material or source (if available). Statements addressing determinability are sometimes required as part of the test method procedure in order to provide early warning of a significant degradation of testing quality while processing any series of samples.  
5.2 Repeatability and reproducibility are defined in the precision section of every Committee D02 test method. Determinability is defined above in Section 3. The relationship among the three measures of precision can be tabulated in terms of their different sources of variation (see Table 1).  
5.2.1 When used, determinability is a mandatory part of the Procedure section. It will allow operators to check their technique for the sequence of operations specified. It also ensures that a result based on the set of determined values is not subject to excessive variability from that source.  
5.3 A bias statement furnishes guidelines on the relationship between a set of test results and a related set of accepted reference values. When the bias of a test method is known, a compensating adjustment can be incorporated in the test method.  
5.4 This practice is intended for use by D02 subcommittees in determining precision estimates and bias statements to be used in D02 test methods. Its procedures correspond with ISO 4259 and are the basis for the Committee D02 computer software, Calculation of Precision Data: Petroleum Test Methods. The use of this practice replaces that of Re...
SCOPE
1.1 This practice covers the necessary preparations and planning for the conduct of interlaboratory programs for the development of estimates of precision (determinability, repeatability, and reproducibility) and of bias (absolute and relative), and further presents the standard phraseology for incorporating such information into standard test methods.  
1.2 This practice is generally limited to homogeneous petroleum products, liquid fuels, and lubricants with which serious sampling problems (such as heterogeneity or instability) do not normally arise.  
1.3 This practice may not be suitable for products with sampling problems as described in 1.2, solid or semisolid products such as petroleum coke, industrial pitches, paraffin waxes, greases, or solid lubricants when the heterogeneous properties of the substances create sampling problems. In such instances, consult a trained statistician.  
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.

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