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ASTM D4007-08

(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
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.
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 D 4006 (API MPMS Chapter 10.2) (Note 1), and sediment by extraction, Test Method D 473 (API MPMS Chapter 10.1), shall be used.
Note 1—Test Method D 4006 (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 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 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
29-Feb-2008
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 D4007-02(2006) - Standard Test Method for Water and Sediment in Crude Oil by the Centrifuge Method (Laboratory Procedure)
Effective Date
01-Mar-2008
Replaced By
ASTM D4007-11 - Standard Test Method for Water and Sediment in Crude Oil by the Centrifuge Method (Laboratory Procedure)
Effective Date
01-Jun-2011
Referred By
ASTM F2709-19 - Standard Test Method for Determining a Measured Nameplate Recovery Rate of Stationary Oil Skimmer Systems
Effective Date
01-Mar-2008
Referred By
ASTM F631-15(2020) - Standard Guide for Collecting Skimmer Performance Data in Controlled Environments
Effective Date
01-Mar-2008
Referred By
ASTM D4177-22e1 - Standard Practice for Automatic Sampling of Petroleum and Petroleum Products
Effective Date
01-Mar-2008
Referred By
ASTM D7666-12(2019) - Standard Specification for Triglyceride Burner Fuel
Effective Date
01-Mar-2008
Referred By
ASTM F2084/F2084M-01(2018) - Standard Guide for Collecting Containment Boom Performance Data in Controlled Environments
Effective Date
01-Mar-2008
Referred By
ASTM F3350-18 - Standard Guide for Collecting Skimmer Performance Data in Ice Conditions
Effective Date
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ASTM F1084-08(2018) - Standard Guide for Sampling Oil/Water Mixtures for Oil Spill Recovery Equipment
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ASTM D4007-08 - Standard Test Method for Water and Sediment in Crude Oil by the Centrifuge Method (Laboratory Procedure)ASTM D4007-08 - Standard Test Method for Water and Sediment in Crude Oil by the Centrifuge Method (Laboratory Procedure)
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REDLINE ASTM D4007-08 - Standard Test Method for Water and Sediment in Crude Oil by the Centrifuge Method (Laboratory Procedure)REDLINE ASTM D4007-08 - 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:D4007–08
Designation: 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* D665 Test Method for Rust-Preventing Characteristics of
Inhibited Mineral Oil in the Presence of Water
1.1 This test method describes the laboratory determination
D1796 TestMethodforWaterandSedimentinFuelOilsby
of water and sediment in crude oils by means of the centrifuge
the Centrifuge Method (Laboratory Procedure)
procedure. This centrifuge method for determining water and
D4006 Test Method for Water in Crude Oil by Distillation
sediment in crude oils is not entirely satisfactory. The amount
D4057 Practice for Manual Sampling of Petroleum and
of water detected is almost always lower than the actual water
Petroleum Products
content. When a highly accurate value is required, the revised
D4177 Practice for Automatic Sampling of Petroleum and
procedures for water by distillation, Test Method D4006 (API
Petroleum Products
MPMS Chapter 10.2) (Note 1), and sediment by extraction,
D5854 PracticeforMixingandHandlingofLiquidSamples
Test Method D473 (API MPMS Chapter 10.1), shall be used.
of Petroleum and Petroleum Products
NOTE 1—Test Method D4006 (API MPMS Chapter 10.2) has been
E969 Specification for Glass Volumetric (Transfer) Pipets
determined to be the preferred and most accurate method for the
3
2.2 API Standards:
determination of water.
MPMS Chapter 8.1 Manual Sampling of Petroleum and
1.2 The values stated in SI units are to be regarded as
Petroleum Products (ASTM Practice D4057)
standard. The values given in parentheses are for information
MPMS Chapter 8.2 Automatic Sampling of Petroleum and
only.
Petroleum Products (ASTM Practice D4177)
1.3 This standard does not purport to address all of the
MPMSChapter8.3 MixingandHandlingofLiquidSamples
safety concerns, if any, associated with its use. It is the
of Petroleum and Petroleum Products (ASTM Practice
responsibility of the user of this standard to establish appro-
D5854)
priate safety and health practices and determine the applica-
MPMS Chapter 10.1 Determination of Sediment in Crude
bility of regulatory limitations prior to use. Specific warning
Oils and Fuel Oils by the Extraction Method (ASTMTest
statements appear in 6.1, 8.3, and A1.5.4.
Method D473)
MPMS Chapter 10.2 Determination of Water in Crude Oil
2. Referenced Documents
by Distillation (ASTM Test Method D4006)
2
2.1 ASTM Standards:
MPMS Chapter 10.4 Determination of Sediment and Water
D95 Test Method for Water in Petroleum Products and
in Crude Oil by the Centrifuge Method (Field Procedure)
Bituminous Materials by Distillation
MPMS Chapter 10.5 Determination of Water in Petroleum
D473 TestMethodforSedimentinCrudeOilsandFuelOils
Products and Bituminous Materials by Distillation
by the Extraction Method
(ASTM Test Method D95)
MPMS Chapter 10.6 Determination of Water and Sediment
in Fuel Oils by the Centrifuge Method (Laboratory Pro-
1
This test method is under the jurisdiction of ASTM Committee D02 on
cedures) (ASTM Test Method D1796)
Petroleum Products and Lubricants and theAPI Committee on Petroleum Measure-
4
2.3 IP Standard:
ment, and is the direct responsibility of Subcommittee D02.02.10 on Sediment and
Water (API MPMS Chapter 10.0).
Methods Book, Appendix B Specification for Methylben-
Current edition approved March 1, 2008. Published April 2008. Originally
zenes (Toluenes)
approved in 1981. Last previous edition approved in 2006 as D4007–02(2006).
DOI: 10.1520/D4007-08.
This test method was issued as a joint ASTM-API-IP standard in 1981.
2 3
For referenced ASTM standards, visit the ASTM website, www.astm.org, or Available from American Petroleum Institute (API), 1220 L. St., NW, Wash-
contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM ington, DC 20005-4070, www.api.org.
4
Standards volume information, refer to the standard’s Document Summary page on Available from Energy Institute, 61 New Cavendish St., London, WIG 7AR,
the ASTM website. U.K., http://www.energyinst.org.uk.
*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 ----------------------
D4007–08
5
2.4 ISO Standard: 5.1.6 Calculate the relative centrifugal force from a mea-
ISO 5272:1979 Toluene for Industrial Use—Specificatio
...

This document is not anASTM standard and is intended only to provide the user of anASTM 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.
An American National Standard
Designation:D4007–02 (Reapproved 2006) Designation:D4007–08
Designation: 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 (e) indicates an editorial change since the last revision or reapproval.
1. 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 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 and health practices and determine the applicability of regulatory
limitations prior to use. For specific precautionary statements, see 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)
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)
MPMS Chapter 10.1 Determination of Sediment in Crude Oils and Fuel Oils by the Extraction Method (ASTM Test Method
D473)
MPMS Chapter 10.2 Determination of Water in Crude Oil by Distillation (ASTM Test Method D4006)
1
This test method is under the jurisdiction ofASTM Committee D02 on Petroleum Products and Lubricants and theAPI Committee on Petroleum Measurement, and is
thedirectresponsibilityofSubcommitteeD02.02.0B/COMQ,D02.02/COMQ,thejointASTM-APICommitteeonSampling,Sediment,Water.StaticPetroleumMeasurement.
Current edition approved Nov.March 1, 2006.2008. Published December 2006.April 2008. Originally approved in 1981. Last previous edition approved in 20022006 as
D4007–02. D4007–02(2006).
ThistestmethodhasbeenapprovedbythesponsoringcommitteesandacceptedbytheCooperatingSocietiesinaccordancewithestablishedprocedures.Thismethodwas
issued as a joint ASTM-API-IP standard in 1981.
2
ForreferencedASTMstandards,visittheASTMwebsite,www.astm.org,orcontactASTMCustomerServiceatservice@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, http://api-ec.api.org.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

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ASTM D2892-23(Test Method)
Standard Test Method for Distillation of Crude Petroleum (15-Theoretical Plate Column)

SIGNIFICANCE AND USE
5.1 This test method is one of a number of tests conducted on a crude oil to determine its value. It provides an estimate of the yields of fractions of various boiling ranges and is therefore valuable in technical discussions of a commercial nature.  
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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1.1 This test method covers the procedure for the distillation of stabilized crude petroleum (see Note 1) to a final cut temperature of 400 °C Atmospheric Equivalent Temperature (AET). This test method employs a fractionating column having an efficiency of 14 to 18 theoretical plates operated at a reflux ratio of 5:1. Performance criteria for the necessary equipment is specified. Some typical examples of acceptable apparatus are presented in schematic form. This test method offers a compromise between efficiency and time in order to facilitate the comparison of distillation data between laboratories.
Note 1: Defined as having a Reid vapor pressure less than 82.7 kPa (12 psi).  
1.2 This test method details procedures for the production of a liquefied gas, distillate fractions, and residuum of standardized quality on which analytical data can be obtained, and the determination of yields of the above fractions by both mass and volume. From the preceding information, a graph of temperature versus mass % distilled can be produced. This distillation curve corresponds to a laboratory technique, which is defined at 15/5 (15 theoretical plate column, 5:1 reflux ratio) or TBP (true boiling point).  
1.3 This test method can also be applied to any petroleum mixture except liquefied petroleum gases, very light naphthas, and fractions having initial boiling points above 400 °C.  
1.4 This test method contains the following annexes and appendixes:  
1.4.1 Annex A1—Test Method for the Determination of the Efficiency of a Distillation Column,  
1.4.2 Annex A2—Test Method for the Determination of the Dynamic Holdup of a Distillation Column,  
1.4.3 Annex A3—Test Method for the Determination of the Heat Loss in a Distillation Column (Static Conditions),  
1.4.4 Annex A4—Test Method for the Verification of Temperature Sensor Location,  
1.4.5 Annex A5—Test Method for Determination of the Temperature Response Time,  
1.4.6 Annex A6—Practice for the Calibration of Sensors,  
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1.4.8 Annex A8—Practice for Conversion of Observed Vapor Temperature to Atmospheric Equivalent Temperature (AET),  
1.4.9 Appendix X1—Test Method for Dehydration of a Sample of Wet Crude Oil, and  
1.4.10 Appendix X2—Practice for Performance Check.  
1.5 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.  
1.6 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.  
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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.  
5.2 The quality of crude oil is related to the amount of sulfur present. Knowledge of the vanadium and nickel concentration is necessary for processing purposes as well as contractual agreements.  
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1.1 This test method covers the quantitative determination of total vanadium and nickel in crude and residual oil in the concentration ranges shown in Table 1 using X-ray fluorescence (XRF) spectrometry.  
1.2 Sulfur is measured for analytical purposes only for the compensation of X-ray absorption matrix effects affecting the vanadium and nickel X-rays. For measurement of sulfur by standard test method use Test Methods D4294, D2622 or other suitable standard test method for sulfur in crude and residual oils.  
1.3 This test method is limited to the use of X-ray fluorescence (XRF) spectrometers employing an X-ray tube for excitation in conjunction with wavelength dispersive detection system or energy dispersive high resolution semiconductor detector with the ability to separate signals of adjacent and near-adjacent elements.  
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1.1 This guide covers a summary of the water and sediment determination methods from the API MPMS Chapter 10 for crude oils. The purpose of this guide is to provide a quick reference to these methodologies such that the reader can make the appropriate decision regarding which method to use based on the associated benefits, uses, drawbacks and limitations.  
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5.1 Most often determined trace elements in crude oils are nickel and vanadium, which are usually the most abundant; however, as many as 45 elements in crude oils have been reported. Knowledge of trace elements in crude oil is important because they can have an adverse effect on petroleum refining and product quality. These effects can include catalyst poisoning in the refinery and excessive atmospheric emission in combustion of fuels. Trace element concentrations are also useful in correlating production from different wells and horizons in a field. Elements such as iron, arsenic, and lead are catalyst poisons. Vanadium compounds can cause refractory damage in furnaces, and sodium compounds have been found to cause superficial fusion on fire brick. Some organometallic compounds are volatile which can lead to the contamination of distillate fractions, and a reduction in their stability or malfunctions of equipment when they are combusted.  
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ASTM D8045-17(2023)(Test Method)
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5.1 Crude oils and oil sands bitumen contain naturally occurring acidic species. Acidity of crude oil has been implicated in corrosion of distribution and process systems. The relative amount of these materials can be determined by titrating with bases. The acid number is a measure of this amount of acidic substance in the oil under the conditions of the test.  
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SCOPE
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Standard Test Method for Determination of Intrinsic Stability of Asphaltene-Containing Residues, Heavy Fuel Oils, and Crude Oils (n-Heptane Phase Separation; Optical Detection)

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5.1 This test method describes a sensitive method for estimating the intrinsic stability of an oil. The intrinsic stability is expressed as S-value. An oil with a low S-value is likely to undergo flocculation of asphaltenes when stressed (for example, extended heated storage) or blended with a range of other oils. Two oils each with a high S-value are likely to maintain asphaltenes in a peptized state and not lead to asphaltene flocculation when blended together.  
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1.2 This test method is applicable to residual products from thermal and hydrocracking processes, to products typical of Specifications D396 Grades No. 5L, 5H, and 6, and D2880 Grades No. 3-GT and 4-GT, and to crude oils, providing these products contain 0.5 % by mass or greater concentration of asphaltenes (see Test Method D6560).  
1.3 This test method quantifies asphaltene stability in terms of state of peptization of the asphaltenes (S-value), intrinsic stability of the oily medium (So) and the solvency requirements of the peptized asphaltenes (Sa).  
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.

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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 D8150-22(Test Method)
Standard Test Method for Determination of Organic Chloride Content in Crude Oil by Distillation Followed by Detection Using Combustion Ion Chromatography

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 less than 1 μg/g organic chlorides in the whole crude, and less than 5 μg/g in the light naphtha, based on the yield of naphtha being 20 % of the original sample.
5.1.2.1 To ensure less than 1 μg/g organic chloride in the crude oil, the amount measured in the naphtha fraction shall be less than 1/f (where f is the naphtha fraction calculated with Eq 1). For example, a crude oil sample with 1 μg/g of organic chloride but a 10 % yield of naphtha would create a naphtha containing 10 μg/g organic chloride. Further, a crude containing 1 μg/g of organic chloride but a 40 % yield of naphtha would create a naphtha containing 2.5 μg/g organic chloride. Due to the difference in naphtha yields, the impact on refining operations can be significantly different.
5.1.2.2 Since crude oil deposits worldwide exhibit different yields of naphtha, the working range of detection for this method shall cover a broad range, possibly as high as 50 μg/g in a naphtha fraction.  
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 ...
SCOPE
1.1 This test method covers the determination of organic chloride (above 1 μg/g organically-bound chlorine) in crude oils, using distillation and combustion ion chromatography.  
1.2 This test method involves 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 The test procedure covers the determination of organic chloride in the washed naphtha fraction of crude oil by combustion ion chromatography. Other halides can be determined but are not included in the precision statement of the test method.  
1.4 The values stated in SI units are to be regarded as standard. The preferred concentration units are micrograms of chloride per gram of sample.  
1.4.1 Exception—The values given in parentheses are for information only.  
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.  
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision ...

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