1、Designation: D664 17a British Standard 4457Designation 177/96Standard Test Method forAcid Number of Petroleum Products by PotentiometricTitration1This standard is issued under the fixed designation D664; the number immediately following the designation indicates the year oforiginal adoption or, in t
2、he case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.This standard has been approved for use by agencies of the U.S. Department of Defense.1. Scope*1.
3、1 This test method covers procedures for the determina-tion of acidic constituents in petroleum products, lubricants,biodiesel, and blends of biodiesel.1.1.1 Test Method AFor petroleum products and lubricantssoluble or nearly soluble in mixtures of toluene and propan-2-ol. It is applicable for the d
4、etermination of acids whosedissociation constants in water are larger than 109; extremelyweak acids whose dissociation constants are smaller than 109do not interfere. Salts react if their hydrolysis constants arelarger than 109. The range of acid numbers included in theprecision statement is 0.1 mgg
5、 KOH to 150 mgg KOH.1.1.2 Test Method BDeveloped specifically for biodieseland biodiesel blends with low acidity and slightly differentsolubility. This test method requires the use of an automatictitrator with automatic endpoint-seeking capability.NOTE 1In new and used oils, the constituents that ma
6、y be consideredto have acidic characteristics include organic and inorganic acids, esters,phenolic compounds, lactones, resins, salts of heavy metals, salts ofammonia and other weak bases, acid salts of polybasic acids, and additionagents such as inhibitors and detergents.1.2 The test method may be
7、used to indicate relativechanges that occur in oil during use under oxidizing conditionsregardless of the color or other properties of the resulting oil.Although the titration is made under definite equilibriumconditions, the test method is not intended to measure anabsolute acidic property that can
8、 be used to predict perfor-mance of oil under service conditions. No general relationshipbetween bearing corrosion and acid number is known.NOTE 2The acid number obtained by this standard may or may not benumerically the same as that obtained in accordance with Test MethodsD974 and D3339. There has
9、not been any attempt to correlate this methodwith other non-titration methods.NOTE 3A few laboratories have made the observation that there is adifference in Test Method D664 results when aqueous versus nonaqueousbuffers are used.1.3 The values stated in SI units are to be regarded asstandard. No ot
10、her units of measurement are included in thisstandard.1.4 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibility of the user of this standard to establish appro-priate safety, health, and environmental practices and deter-mine th
11、e applicability of regulatory limitations prior to use.1.5 This international standard was developed in accor-dance with internationally recognized principles on standard-ization established in the Decision on Principles for theDevelopment of International Standards, Guides and Recom-mendations issu
12、ed by the World Trade Organization TechnicalBarriers to Trade (TBT) Committee.2. Referenced Documents2.1 ASTM Standards:2D974 Test Method for Acid and Base Number by Color-Indicator TitrationD1193 Specification for Reagent WaterD3339 Test Method forAcid Number of Petroleum Productsby Semi-Micro Colo
13、r Indicator TitrationD4057 Practice for Manual Sampling of Petroleum andPetroleum ProductsD4177 Practice for Automatic Sampling of Petroleum andPetroleum ProductsE177 Practice for Use of the Terms Precision and Bias inASTM Test Methods3. Terminology3.1 Definitions:1This test method is under the juri
14、sdiction of ASTM Committee D02 onPetroleum Products, Liquid Fuels, and Lubricants and is the direct responsibility ofSubcommittee D02.06 on Analysis of Liquid Fuels and Lubricants.Current edition approved Dec. 15, 2017. Published March 2018. Originallyapproved in 1942. Last previous edition approved
15、 in 2017 as D664 17. DOI:10.1520/D0664-17A.This test method was adopted as a joint ASTM-IP standard in 1964. ASTM TestMethod D4739 has been developed as an alternative to the base number portion ofD664.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Serv
16、ice at serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.*A Summary of Changes section appears at the end of this standardCopyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-
17、2959. United StatesThis international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for theDevelopment of International Standards, Guides and Recommendations issued by the World Trade Organization Technica
18、l Barriers to Trade (TBT) Committee.13.1.1 acid number, nthe quantity of a specified base,expressed in milligrams of potassium hydroxide per gram ofsample, required to titrate a sample in a specified solvent to aspecified endpoint using a specified detection system.3.1.1.1 DiscussionThis test method
19、 expresses the quantityof base as milligrams of potassium hydroxide per gram ofsample, that is required to titrate a sample in a mixture oftoluene and propan-2-ol to which a small amount of water hasbeen added from its initial meter reading in millivolts to ameter reading in millivolts corresponding
20、 to an aqueous basicbuffer solution or a well-defined inflection point as specified inthe test method.3.1.1.2 DiscussionThis test method provides additionalinformation. The quantity of base, expressed as milligrams ofpotassium hydroxide per gram of sample, required to titrate asample in the solvent
21、from its initial meter reading in millivoltsto a meter reading in millivolts corresponding to a freshlyprepared aqueous acidic buffer solution or a well-definedinflection point as specified in the test method shall be reportedas the strong acid number.3.1.1.3 DiscussionThe causes and effects of the
22、so-calledstrong acids and the causes and effects of the other acids can bevery significantly different. Therefore, the user of this testmethod shall differentiate and report the two, when they arefound.4. Summary of Test Method4.1 The sample is dissolved in a titration solvent and titratedpotentiome
23、trically with alcoholic potassium hydroxide using aglass indicating electrode and a reference electrode or acombination electrode. The meter readings are plotted manu-ally or automatically against the respective volumes of titratingsolution and the end points are taken only at well-definedinflection
24、s in the resulting curve. When no definite inflectionsare obtained and for used oils, end points are taken at meterreadings corresponding to those found for aqueous acidic andbasic buffer solutions.5. Significance and Use5.1 New and used petroleum products, biodiesel, and blendsof biodiesel may cont
25、ain acidic constituents that are present asadditives or as degradation products formed during service,such as oxidation products. The relative amount of thesematerials can be determined by titrating with bases. The acidnumber is a measure of this amount of acidic substance in theoil, always under th
26、e conditions of the test. The acid number isused as a guide in the quality control of lubricating oilformulations. It is also sometimes used as a measure oflubricant degradation in service. Any condemning limits mustbe empirically established.5.2 Since a variety of oxidation products contribute to t
27、heacid number and the organic acids vary widely in corrosionproperties, the test method cannot be used to predict corrosive-ness of oil or biodiesel and blends under service conditions. Nogeneral correlation is known between acid number and thecorrosive tendency of biodiesel and blends or oils towar
28、dmetals.6. Apparatus6.1 Manual Titration Apparatus:6.1.1 Meter, a voltmeter or a potentiometer that will operatewith an accuracy of 60.005 V and a sensitivity of 60.002 Vover a range of at least 60.5 V when the meter is used with theelectrodes specified in 6.1.2 and 6.1.3 and when the resistancebetw
29、een the electrodes falls within the range from 0.2 M to20 M. The meter shall be protected from stray electrostaticfields so that no permanent change in the meter readings overthe entire operating range is produced by touching, with agrounded lead, any part of the exposed surface of the glasselectrod
30、e, the glass electrode lead, the titration stand, or themeter.NOTE 4A suitable apparatus could consist of a continuous-readingelectronic voltmeter designed to operate on an input of less than 5 1012A, when an electrode system having 1000 M resistance is connectedacross the meter terminals and provid
31、ed with a metal shield connected tothe ground, as well as a satisfactory terminal to connect the shieldedconnection wire from the glass electrode to the meter without interferencefrom any external electrostatic field.6.1.2 Sensing Electrode, standard pH, suitable for nonaque-ous titrations.6.1.3 Ref
32、erence Electrode, silver/silver chloride (Ag/AgCl)reference electrode, filled with 1M to 3M LiCl in ethanol.6.1.3.1 Combination ElectrodesSensing electrodes mayhave the Ag/AgCl reference electrode built into the sameelectrode body, which offers the convenience of working withand maintaining only one
33、 electrode. The combination electrodeshall have a sleeve junction on the reference compartment andshall use an inert ethanol electrolyte, for example, 1M3MLiCl in ethanol. These combination electrodes shall have thesame response or better response than a dual electrode system.They shall have removab
34、le sleeves for easy rinsing andaddition of electrolyte.NOTE 5A third electrode, such as a platinum electrode, may be usedto increase the electrode stability in certain systems.6.1.4 Variable-Speed Mechanical Stirrer, a suitable type,equipped with a propeller-type stirring paddle. The rate ofstirring
35、 shall be sufficient to produce vigorous agitation withoutspattering and without stirring air into the solution.Apropellerwith blades 6 mm in radius and set at a pitch of 30 to 45 issatisfactory. A magnetic stirrer is also satisfactory.6.1.4.1 If an electrical stirring apparatus is used, it shall be
36、electrically correct and grounded so that connecting or discon-necting the power to the motor will not produce a permanentchange in the meter reading during the course of the titration.6.1.5 Burette, 10 mL capacity, graduated in 0.05 mL divi-sions and calibrated with an accuracy of 60.02 mL. Thebure
37、tte shall have a tip that extends 100 mm to 130 mm beyondthe stopcock and shall be able to deliver titrant directly into thetitration vessel without exposure to the surrounding air orvapors.The burette for KOH shall have a guard tube containingsoda lime or other CO2-absorbing substance.6.1.6 Titrati
38、on Beaker, 250 mL, 125 mL, or suitablecapacity, made of borosilicate glass or other suitable material.6.1.7 Titration Stand, suitable for supporting the electrodes,stirrer, and burette.D664 17a2NOTE 6An arrangement that allows the removal of the beaker withoutdisturbing the electrodes and stirrer is
39、 desirable.6.2 Automatic Titration Apparatus:6.2.1 Automatic titration systems shall be able to carry outthe necessary analyses as prescribed in the method. As aminimum, the automatic titration system shall meet the perfor-mance and specification requirements listed in 6.1 as war-ranted.6.2.2 A dyna
40、mic mode of titrant addition shall be used.During the titration, the speed and volume of the addition shallvary depending on the rate of change of the system. Therecommended maximum volume increment is 0.5 mL and therecommended minimum volume increment is 0.05 mL.6.2.3 Graduated Cylinder50 mL, or di
41、spensing devicecapable of delivering 50 mL 6 0.5 mL.6.2.4 Pipette2.0 mL, Class A.6.2.5 Titration Beaker250 mL, 125 mL, or suitablecapacity, made of borosilicate glass or other suitable material.7. Reagents7.1 Purity of ReagentsReagent-grade chemicals shall beused in all tests. Unless otherwise indic
42、ated, it is intended thatall reagents shall conform to the specifications of the commit-tee on Analytical Reagents of the American Chemical Society,where such specifications are available.3Other grades may beused, provided it is first ascertained that the reagent is ofsufficiently high purity to per
43、mit its use without lessening theaccuracy of the determination.7.1.1 Commercially available solutions may be used inplace of laboratory preparations, provided the solutions havebeen certified as being equivalent.7.1.2 Alternate volumes of the solutions may be prepared,provided the final solution con
44、centration is equivalent.7.2 Purity of WaterUnless otherwise indicated, referenceto water shall be understood to mean reagent water that meetsthe requirements of either Type I, II, or III of SpecificationD1193.7.3 Primary StandardWhere specified, these samples, orsamples of commercially available pr
45、imary standards, are to beused in standardizing the volumetric solutions.7.4 Ethanol. (WarningFlammable and toxic, especiallywhen denatured.)7.5 Lithium Chloride, LiCl.7.6 Lithium Chloride Electrolyte, Prepare a 1M3M solu-tion of lithium chloride (LiCl) in ethanol.7.7 Potassium Hydroxide. (WarningCa
46、uses severeburns.)7.8 Propan-2-ol, Anhydrous, (less than 0.1 % H2O).(WarningFlammable.) If adequately dry reagent cannot beprocured, it can be dried by distillation through a multiple platecolumn, discarding the first 5 % of material distilling overheadand using the 95 % remaining. Drying can also b
47、e accom-plished using molecular sieves such as Linde Type 4A, bypassing the solvent upward through a molecular sieve columnusing one part of molecular sieve per ten parts of solvent.NOTE 7It has been reported that, if not originally inhibited against it,propan-2-ol can contain peroxides. When this o
48、ccurs, an explosion ispossible when the storage of the vessel or other equipment such as adispensing bottle, is near empty and approaching dryness.7.9 Commercial Aqueous pH 4, pH 7, and pH 11 BufferSolutionsThese solutions shall be replaced at regular inter-vals consistent with their stability or wh
49、en contamination issuspected. Information relating to their stability should beobtained from the manufacturer.8. Electrode System8.1 Preparation of ElectrodesWhen a Ag/AgCl referenceelectrode is used for the titration and it contains an electrolytewhich is not 1M3M LiCl in ethanol, replace the electrolyte.Drain the electrolyte from the electrode, wash away all the salt(if present) with water and then rinse with ethanol. Rinseseveral times with the LiCl electrolyte solution. Finally, replacethe sleeve and fill the electrode with the LiCl elect
