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ASTM D4007-11(2016)

(Test Method)

Standard Test Method for Water and Sediment in Crude Oil by the Centrifuge Method (Laboratory Procedure)

Standard Test Method for Water and Sediment in Crude Oil by the Centrifuge Method (Laboratory Procedure)

SIGNIFICANCE AND USE
4.1 The water and sediment content of crude oil is significant because it can cause corrosion of equipment and problems in processing. A determination of water and sediment content is required to measure accurately net volumes of actual oil in sales, taxation, exchanges, and custody transfers. It is not anticipated that this test method, which is written with a dedicated laboratory facility in mind, is likely to be used in field test rooms or sample rooms due to safety concerns for proper ventilation and handling.  
4.2 This test method may not be suitable for crude oils that contain alcohols that are soluble in water. In cases where the impact on the results may be significant, the user is advised to consider using another test method, such as Test Method D4928 (API MPMS Chapter 10.9).
SCOPE
1.1 This test method describes the laboratory determination of water and sediment in crude oils by means of the centrifuge procedure. This centrifuge method for determining water and sediment in crude oils is not entirely satisfactory. The amount of water detected is almost always lower than the actual water content. When a highly accurate value is required, the revised procedures for water by distillation, Test Method D4006 (API MPMS Chapter 10.2) (Note 1), and sediment by extraction, Test Method D473 (API MPMS Chapter 10.1), shall be used.  
Note 1: Test Method D4006 (API MPMS Chapter 10.2) has been determined to be the preferred and most accurate method for the determination of water.  
1.2 The values stated in SI units are to be regarded as 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 and health practices and determine the applicability of regulatory limitations prior to use. Specific warning statements appear in 6.1, 8.3, and A1.5.4.

General Information

Status
Historical
Publication Date
31-May-2016
ICS
75.040 - Crude petroleum
Technical Committee
D02 - Petroleum Products, Liquid Fuels, and Lubricants
Drafting Committee
D02.02 - Hydrocarbon Measurement for Custody Transfer (Joint ASTM-API)
Current Stage
Ref Project

Relations

Replaces
ASTM D4007-11e1 - Standard Test Method for Water and Sediment in Crude Oil by the Centrifuge Method (Laboratory Procedure)
Effective Date
01-Jun-2016
Referred By
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01-Jun-2016
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ASTM F1084-08(2018) - Standard Guide for Sampling Oil/Water Mixtures for Oil Spill Recovery Equipment
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01-Jun-2016
Referred By
ASTM F3350-18 - Standard Guide for Collecting Skimmer Performance Data in Ice Conditions
Effective Date
01-Jun-2016
Referred By
ASTM D7666-12(2019) - Standard Specification for Triglyceride Burner Fuel
Effective Date
01-Jun-2016
Referred By
ASTM F2709-19 - Standard Test Method for Determining a Measured Nameplate Recovery Rate of Stationary Oil Skimmer Systems
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01-Jun-2016
Referred By
ASTM F2084/F2084M-01(2018) - Standard Guide for Collecting Containment Boom Performance Data in Controlled Environments
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ASTM D4177-22e1 - Standard Practice for Automatic Sampling of Petroleum and Petroleum Products
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ASTM D4007-11(2016) - Standard Test Method for Water and Sediment in Crude Oil by the Centrifuge Method (Laboratory Procedure)ASTM D4007-11(2016) - Standard Test Method for Water and Sediment in Crude Oil by the Centrifuge Method (Laboratory Procedure)
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REDLINE ASTM D4007-11(2016) - Standard Test Method for Water and Sediment in Crude Oil by the Centrifuge Method (Laboratory Procedure)REDLINE ASTM D4007-11(2016) - Standard Test Method for Water and Sediment in Crude Oil by the Centrifuge Method (Laboratory Procedure)
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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: D4007 − 11 (Reapproved 2016)
Manual of Petroleum Measurement Standards (MPMS), Chapter 10.3
Standard Test Method for
Water and Sediment in Crude Oil by the Centrifuge Method
1
(Laboratory Procedure)
This standard is issued under the fixed designation D4007; 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 (´) indicates an editorial change since the last revision or reapproval.
1. Scope BituminousMaterialsbyDistillation(API MPMSChapter
10.5)
1.1 This test method describes the laboratory determination
D473TestMethodforSedimentinCrudeOilsandFuelOils
of water and sediment in crude oils by means of the centrifuge
by the Extraction Method (API MPMS Chapter 10.1)
procedure. This centrifuge method for determining water and
D665Test Method for Rust-Preventing Characteristics of
sediment in crude oils is not entirely satisfactory. The amount
Inhibited Mineral Oil in the Presence of Water
of water detected is almost always lower than the actual water
D1796Test Method for Water and Sediment in Fuel Oils by
content. When a highly accurate value is required, the revised
the Centrifuge Method (Laboratory Procedure) (API
procedures for water by distillation, Test Method D4006 (API
MPMS Chapter 10.6)
MPMS Chapter 10.2) (Note 1), and sediment by extraction,
D4006Test Method for Water in Crude Oil by Distillation
Test Method D473 (API MPMS Chapter 10.1), shall be used.
(API MPMS Chapter 10.2)
NOTE 1—Test Method D4006 (API MPMS Chapter 10.2) has been
D4057Practice for Manual Sampling of Petroleum and
determined to be the preferred and most accurate method for the
Petroleum Products (API MPMS Chapter 8.1)
determination of water.
D4177Practice for Automatic Sampling of Petroleum and
1.2 The values stated in SI units are to be regarded as
Petroleum Products (API MPMS Chapter 8.2)
standard.
D4928Test Method forWater in Crude Oils by Coulometric
1.2.1 Exception—The values given in parentheses are for
Karl Fischer Titration (API MPMS Chapter 10.9)
information only.
D5854Practice for Mixing and Handling of Liquid Samples
1.3 This standard does not purport to address all of the
of Petroleum and Petroleum Products (API MPMS Chap-
safety concerns, if any, associated with its use. It is the
ter 8.3)
responsibility of the user of this standard to establish appro- E969Specification for Glass Volumetric (Transfer) Pipets
3
priate safety and health practices and determine the applica-
2.2 API Standards:
bility of regulatory limitations prior to use. Specific warning
MPMS Chapter 8.1Manual Sampling of Petroleum and
statements appear in 6.1, 8.3, and A1.5.4.
Petroleum Products (ASTM Practice D4057)
MPMS Chapter 8.2Automatic Sampling of Petroleum and
2. Referenced Documents
Petroleum Products (ASTM Practice D4177)
2
2.1 ASTM Standards:
MPMSChapter8.3MixingandHandlingofLiquidSamples
D95Test Method for Water in Petroleum Products and
of Petroleum and Petroleum Products (ASTM Practice
D5854)
MPMS Chapter 10.1Determination of Sediment in Crude
1
This test method is under the jurisdiction of ASTM Committee D02 on
Oils and Fuel Oils by the Extraction Method (ASTMTest
Petroleum Products, Liquid Fuels, and Lubricants and the API Committee on
Method D473)
Petroleum Measurement and is the direct responsibility of Subcommittee D02.02
/COMQ the joint ASTM-API Committee on Hydrocarbon Measurement for
MPMSChapter10.2DeterminationofWaterinCrudeOilby
Custody Transfer (Joint ASTM-API). This test method has been approved by the
Distillation (ASTM Test Method D4006)
sponsoring committees and accepted by the Cooperating Societies in accordance
MPMS Chapter 10.4Determination of Sediment and Water
with established procedures.
in Crude Oil by the Centrifuge Method (Field Procedure)
CurrenteditionapprovedJune1,2016.PublishedJuly2016.Originallyapproved
ɛ1
in 1981. Last previous edition approved in 2011 as D4007–11 . DOI: 10.1520/
MPMS Chapter 10.5Determination of Water in Petroleum
D4007-16.
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 American Petroleum Institute (API), 1220 L. St., NW,
the ASTM website. Washington, DC 20005-4070, www.api.org.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States
1

---------------------- Page: 1 ----------------------
D4007 − 11 (2016)
Products and Bituminous Materials by Distillation be capable of maintaining the temperature within these limits
(ASTM Test Method D95) and operate safely if there is a flammable atmosphere.
MPMS Cha
...

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.
´1
Designation: D4007 − 11 D4007 − 11 (Reapproved 2016)
Manual of Petroleum Measurement Standards (MPMS), Chapter 10.3
Standard Test Method for
Water and Sediment in Crude Oil by the Centrifuge Method
1
(Laboratory Procedure)
This standard is issued under the fixed designation D4007; 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
ε NOTE—Referenced Documents and API information was editorially corrected in July 2013.
1. Scope*Scope
1.1 This test method describes the laboratory determination of water and sediment in crude oils by means of the centrifuge
procedure. This centrifuge method for determining water and sediment in crude oils is not entirely satisfactory. The amount of
water detected is almost always lower than the actual water content. When a highly accurate value is required, the revised
procedures for water by distillation, Test Method D4006 (API MPMS Chapter 10.2) (Note 1), and sediment by extraction, Test
Method D473 (API MPMS Chapter 10.1), shall be used.
NOTE 1—Test Method D4006 (API MPMS Chapter 10.2) has been determined to be the preferred and most accurate method for the determination of
water.
1.2 The values stated in SI units are to be regarded as standard. The values given in parentheses are for information only.
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 and health practices and determine the applicability of regulatory
limitations prior to use. Specific warning statements appear in 6.1, 8.3, and A1.5.4.
2. Referenced Documents
2
2.1 ASTM Standards:
D95 Test Method for Water in Petroleum Products and Bituminous Materials by Distillation (API MPMS Chapter 10.5)
D473 Test Method for Sediment in Crude Oils and Fuel Oils by the Extraction Method (API MPMS Chapter 10.1)
D665 Test Method for Rust-Preventing Characteristics of Inhibited Mineral Oil in the Presence of Water
D1796 Test Method for Water and Sediment in Fuel Oils by the Centrifuge Method (Laboratory Procedure) (API MPMS Chapter
10.6)
D4006 Test Method for Water in Crude Oil by Distillation (API MPMS Chapter 10.2)
D4057 Practice for Manual Sampling of Petroleum and Petroleum Products (API MPMS Chapter 8.1)
D4177 Practice for Automatic Sampling of Petroleum and Petroleum Products (API MPMS Chapter 8.2)
D4928 Test Method for Water in Crude Oils by Coulometric Karl Fischer Titration (API MPMS Chapter 10.9)
D5854 Practice for Mixing and Handling of Liquid Samples of Petroleum and Petroleum Products (API MPMS Chapter 8.3)
E969 Specification for Glass Volumetric (Transfer) Pipets
3
2.2 API Standards:
MPMS Chapter 8.1 Manual Sampling of Petroleum and Petroleum Products (ASTM Practice D4057)
MPMS Chapter 8.2 Automatic Sampling of Petroleum and Petroleum Products (ASTM Practice D4177)
MPMS Chapter 8.3 Mixing and Handling of Liquid Samples of Petroleum and Petroleum Products (ASTM Practice D5854)
1
This test method is under the jurisdiction of ASTM Committee D02 on Petroleum Products, Liquid Fuels, and Lubricants and the API Committee on Petroleum
Measurement and is the direct responsibility of Subcommittee D02.02 /COMQ the joint ASTM-API Committee on Hydrocarbon Measurement for Custody Transfer (Joint
ASTM-API). This test method has been approved by the sponsoring committees and accepted by the Cooperating Societies in accordance with established procedures.
Current edition approved June 1, 2011June 1, 2016. Published August 2011July 2016. Originally approved in 1981. Last previous edition approved in 20082011 as
ɛ1
D4007D4007 – 11 –08. DOI: 10.1520/D4007-11E01.10.1520/D4007-16.
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 Standards
volume information, refer to the standard’s Document Summary page on the ASTM website.
3
Available from American Petroleum Institute (API), 1220 L. St., NW, Washington, DC 20005-4070, www.api.org.
*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

---------------------- Pa
...

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ASTM D8252-23(Test Method)
Standard Test Method for Vanadium and Nickel in Crude and Residual Oil by X-ray Spectrometry

SIGNIFICANCE AND USE
5.1 This test method provides a rapid and precise elemental measurement with simple sample preparation. Typical analysis times are approximately 4 min to 5 min per sample with a preparation time of approximately 1 min to 3 min per sample.  
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5.2 This test method corresponds to the standard laboratory distillation efficiency referred to as 15/5. The fractions produced can be analyzed as produced or combined to produce samples for analytical studies, engineering, and product quality evaluations. The preparation and evaluation of such blends is not part of this test method.  
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Note 1: Defined as having a Reid vapor pressure less than 82.7 kPa (12 psi).  
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SCOPE
1.1 This test method covers the determination of acidic components in crude oil and petroleum products including waxes, bitumen, base stocks, and asphalts that are soluble in mixtures of xylenes and propan-2-ol. It is applicable for the determination of acids whose dissociation constants in water are larger than 10–9; extremely weak acids whose dissociation constants are smaller than 10–9 do not interfere. The values obtained by this test method may not be numerically equivalent to other acid value measurements. The range of KOH acid numbers included in the precision statement is 0.1 mg/g to 16 mg/g.  
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. Some specific hazards statements are given in Section 7 on Safety Precautions.  
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 D5863-22(Test Method)
Standard Test Methods for Determination of Nickel, Vanadium, Iron, and Sodium in Crude Oils and Residual Fuels by Flame Atomic Absorption Spectrometry

SIGNIFICANCE AND USE
5.1 When fuels are combusted, metals present in the fuels can form low melting compounds that are corrosive to metal parts. Metals present at trace levels in petroleum can deactivate catalysts during processing. These test methods provide a means of quantitatively determining the concentrations of vanadium, nickel, iron, and sodium. Thus, these test methods can be used to aid in determining the quality and value of the crude oil and residual oil.
SCOPE
1.1 These test methods cover the determination of nickel, vanadium, iron, and sodium in crude oils and residual fuels by flame atomic absorption spectrometry (AAS). Two different test methods are presented.  
1.2 Procedure A, Sections 8–14—Flame AAS is used to analyze a sample that is decomposed with acid for the determination of total Ni, V, and Fe.  
1.3 Procedure B, Sections 15–20—Flame AAS is used to analyze a sample diluted with an organic solvent for the determination of Ni, V, and Na. This test method uses oil-soluble metals for calibration to determine dissolved metals and does not purport to quantitatively determine nor detect insoluble particulates. Hence, this test method may underestimate the metal content, especially sodium, present as inorganic sodium salts.  
1.4 The concentration ranges covered by these test methods are determined by the sensitivity of the instruments, the amount of sample taken for analysis, and the dilution volume. A specific statement is given in Note 1.  
1.5 For each element, each test method has its own unique precision. The user can select the appropriate test method based on the precision required for the specific analysis.  
1.6 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard, unless specifically stated. Other units that appear in this standard are included for information purposes only or because they are in embedded pictures that cannot be edited.  
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 8.1, 9.2, 9.5, 11.2, 11.4, and 16.1.  
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.

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ASTM
ASTM D8003-22(Test Method)
Standard Test Method for Determination of Light Hydrocarbons and Cut Point Intervals in Live Crude Oils and Condensates by Gas Chromatography

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.

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ASTM
ASTM D4310-22a(Test Method)
Standard Test Method for Determination of Sludging and Corrosion Tendencies of Inhibited Mineral Oils

SIGNIFICANCE AND USE
5.1 Insoluble material may form in oils that are subjected to oxidizing conditions.  
5.2 Significant formation of oil insolubles or metal corrosion products, or both, during this test may indicate that the oil will form insolubles or corrode metals, or both, during field service. However, no correlation with field service has been established.
SCOPE
1.1 This test method covers and is used to evaluate the tendency of inhibited mineral oil based steam turbine lubricants and mineral oil based anti-wear hydraulic oils to corrode copper catalyst metal and to form sludge during oxidation in the presence of oxygen, water, and copper and iron metals at an elevated temperature. The test method is also used for testing circulating oils having a specific gravity less than that of water and containing rust and oxidation inhibitors.  
Note 1: During round robin testing copper and iron in the oil, water and sludge phases were measured. However, the values for the total iron were found to be so low (that is, below 0.8 mg), that statistical analysis was inappropriate. The results of the cooperative test program are available (see Section 16).  
1.2 This test method is a modification of Test Method D943 where the oxidation stability of the same kinds of oils is determined by following the acid number of oil. The number of test hours required for the oil to reach an acid number of 2.0 mg KOH/g is the oxidation lifetime.  
1.3 Procedure A of this test method requires the determination and report of the weight of the sludge and the total amount of copper in the oil, water, and sludge phases. Procedure B requires the sludge determination only. The acid number determination is optional for both procedures.  
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 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. For specific warning statements, see Section 7 and X1.1.5.  
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
ASTM D4929-22(Test Method)
Standard Test Method for Determination of Organic Chloride Content in Crude Oil

SIGNIFICANCE AND USE
5.1 Organic chlorides do not occur naturally in crude oil. When present, they result from contamination in some manner, such as disposal of chlorinated solvent used in many dewaxing pipeline or other equipment operations.  
5.1.1 Uncontaminated crude oil will contain no detectable organic chloride, and most refineries can handle very small amounts without deleterious effects.
5.1.1.1 Most trade contracts specify that no organic chloride is present in the crude oil.  
5.1.2 Several pipelines have set specification limits at  
5.1.2.1 To ensure Eq 3).  
5.1.3 Organic chloride present in the crude oil (for example, methylene chloride, perchloroethylene, etc.) is usually distilled into the naphtha fraction. Some compounds break down during fractionation and produce hydrochloric acid, which has a corrosive effect. Some compounds survive fractionation and are destroyed during hydro-treating (desulfurization of the naphtha).  
5.2 Other halides can also be used for dewaxing crude oil; in such cases, any organic halides will have similar impact on the refining operations as the organic chlorides.  
5.3 Organic chloride species are potentially damaging to refinery processes. Hydrochloric acid can be produced in hydrotreating or reforming reactors and the acid accumulates in condensing regions of the refinery. Unexpected concentrations of organic chlorides cannot be effectively neutralized and damage can result. Organic chlorides are not known to be naturally present in crude oils and usually result from cleaning operations at producing sites, pipelines, or tanks. It is important for the oil industry to have common methods available for the determination of organic chlorides in crude oil, particularly when transfer of custody is involved.
SCOPE
1.1 The procedures in this test method cover the determination of organic chloride (above 1 μg/g organically-bound chlorine) in crude oils, using either distillation and sodium biphenyl reduction, distillation and microcoulometry, or distillation and X-ray fluorescence (XRF) spectrometry.  
1.2 The procedures in this test method involve the distillation of crude oil test specimens to obtain a naphtha fraction prior to chloride determination. The chloride content of the naphtha fraction of the whole crude oil can thereby be obtained. See Section 6 regarding potential interferences.  
1.3 Procedure A covers the determination of organic chloride in the washed naphtha fraction of crude oil by sodium biphenyl reduction followed by potentiometric titration.  
1.4 Procedure B covers the determination of organic chloride in the washed naphtha fraction of crude oil by oxidative combustion followed by microcoulometric titration.  
1.5 Procedure C covers the determination of organic chloride in the washed naphtha fraction of crude oil by X-ray fluorescence spectrometry.  
1.6 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.6.1 The preferred concentration units are micrograms of chloride per gram of sample, though milligrams of chloride per kilogram of sample is commonly used for Procedure C.  
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.

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