ASTM D4742-2008e1 Standard Test Method for Oxidation Stability of Gasoline Automotive Engine Oils by Thin-Film Oxygen Uptake (TFOUT)《用氧化薄膜吸收法对汽车发动机油氧化稳定性的标准试验方法》.pdf

《ASTM D4742-2008e1 Standard Test Method for Oxidation Stability of Gasoline Automotive Engine Oils by Thin-Film Oxygen Uptake (TFOUT)《用氧化薄膜吸收法对汽车发动机油氧化稳定性的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D4742-2008e1 Standard Test Method for Oxidation Stability of Gasoline Automotive Engine Oils by Thin-Film Oxygen Uptake (TFOUT)《用氧化薄膜吸收法对汽车发动机油氧化稳定性的标准试验方法》.pdf（9页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D4742 081Standard Test Method forOxidation Stability of Gasoline Automotive Engine Oils byThin-Film Oxygen Uptake (TFOUT)1This standard is issued under the fixed designation D4742; the number immediately following the designation indicates the year oforiginal adoption or, in the case of

2、 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.1NOTEUpdated units statement in 1.3 and improved figure quality editorially in November 2009.1. Scope*1.1 T

3、his test method evaluates the oxidation stability ofengine oils for gasoline automotive engines. This test, run at160C, utilizes a high pressure reactor pressurized with oxygenalong with a metal catalyst package, a fuel catalyst, and waterin a partial simulation of the conditions to which an oil may

4、 besubjected in a gasoline combustion engine. This test methodcan be used for engine oils with viscosity in the range from 4mm2/s (cSt) to 21 mm2/s (cSt) at 100C, including re-refinedoils.1.2 This test method is not a substitute for the engine testingof an engine oil in established engine tests, suc

5、h as SequenceIIID.1.3 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.3.1 ExceptionPressure units are provided in psig, anddimensions are provided in inches in Annex A1, because theseare the industry accepted standard and the

6、apparatus is builtaccording to the figures shown.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 and health practices and determine the applica-bility of re

7、gulatory limitations prior to use. For specificwarning statements, see Sections 7 and 8.2. Referenced Documents2.1 ASTM Standards:2A314 Specification for Stainless Steel Billets and Bars forForgingB211 Specification for Aluminum and Aluminum-AlloyBar, Rod, and WireD664 Test Method for Acid Number of

8、 Petroleum Productsby Potentiometric TitrationD1193 Specification for Reagent WaterD2272 Test Method for Oxidation Stability of Steam Tur-bine Oils by Rotating Pressure VesselD4057 Practice for Manual Sampling of Petroleum andPetroleum ProductsE1 Specification for ASTM Liquid-in-Glass Thermometers3.

9、 Terminology3.1 Definitions of Terms Specific to This Standard:3.1.1 break pointthe precise point of time at which rapidoxidation of the oil begins.3.1.2 oxidation induction timethe time until the oil beginsto oxidize at a relatively rapid rate as indicated by the decreaseof oxygen pressure.3.1.3 ox

10、ygen uptakeoxygen absorbed by oil as a result ofoil oxidation.4. Summary of Test Method4.1 The test oil is mixed in a glass container with three otherliquids that are used to simulate engine conditions: (1)anoxidized/nitrated fuel component (Annex A2), (2) a mixture ofsoluble metal naphthenates (lea

11、d, copper, iron, manganese, andtin naphthenates (Annex A3), and (3) Type I reagent water.4.2 The glass container holding the oil mixture is placed ina high pressure reactor equipped with a pressure gauge. Thehigh pressure reactor is sealed, charged with oxygen to apressure of 620 kPa (90 psig), and

12、placed in an oil bath at160C at an angle of 30 from the horizontal. The high pressurereactor is rotated axially at a speed of 100 r/min forming a thinfilm of oil within the glass container resulting in a relativelylarge oil-oxygen contact area.NOTE 1A pressure sensing device can be used in place of

13、a pressuregauge.1This test method is under the jurisdiction of ASTM Committee D02 onPetroleum Products and Lubricants and is the direct responsibility of SubcommitteeD02.09.0G on Oxidation Testing of Engine Oils.Current edition approved Oct. 15, 2008. Published November 2008. Originallyapproved in 1

14、988. Last previous edition approved in 2002 as D474202a. DOI:10.1520/D4742-08E01.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page

15、 onthe ASTM website.1*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.4.3 The pressure of the high pressure reactor is recordedcontinuously from the beginning of the tes

16、t and the test isterminated when a rapid decrease of the high pressure reactorpressure is observed (Point B, Fig. A1.2). The period of timethat elapses between the time when the high pressure reactor isplaced in the oil bath and the time at which the pressure beginsto decrease rapidly is called the

17、oxidation induction time and isused as a measure of the relative oil oxidation stability.5. Significance and Use5.1 This test method is used to evaluate oxidation stabilityof lubricating base oils with additives in the presence ofchemistries similar to those found in gasoline engine service.Test res

18、ults on some ASTM reference oils have been found tocorrelate with sequence IIID engine test results in hours for a375 % viscosity increase.3The test does not constitute asubstitute for engine testing, which measures wear, oxidationstability, volatility, and deposit control characteristics of lubri-c

19、ants. Properly interpreted, the test may provide input on theoxidation stability of lubricants under simulated engine chem-istry.5.2 This test method is intended to be used as a benchscreening test and quality control tool for lubricating base oilmanufacturing, especially for re-refined lubricating

20、base oils.This test method is useful for quality control of oxidationstability of re-refined oils from batch to batch.5.3 This test method is useful for screening formulated oilsprior to engine tests. Within similar additive chemistry andbase oil types, the ranking of oils in this test appears to be

21、predictive of ranking in engine tests. When oils havingcompletely different additive chemistry or base oil type arecompared, oxidation stability results may not reflect the actualengine test result.5.4 Other oxidation stability test methods have demon-strated that soluble metal catalyst supplies are

22、 very inconsistentand they have significant effects on the test results. Thus, fortest comparisons, the same source and same batch of metalnaphthenates shall be used.NOTE 2It is also recommended as a good research practice not to usedifferent batches of the fuel component in test comparisons.6. Appa

23、ratus6.1 High Pressure Reactor, glass sample container, alumi-num insert, pressure gauge, thermometer, test bath and acces-sories are shown in Figs. 2-3 and described in Annex A1.NOTE 3It is reported in literature3that the oxidation high pressurereactor can be modified from the Test Method D2272 oxi

24、dation highpressure reactor by insertion of an aluminum cylinder.3Ku, C. S. and Hsu, S. M., “A Thin Film Uptake Test for the Evaluation ofAutomotive Lubricants,” Lubrication Engineering , 40, 2, 1984, pp. 7583.FIG. 1 Schematic Drawing of Oxidation Test ApparatusD4742 08126.2 Precision Pressure Gauge

25、A certified precision pres-sure gauge is used to accurately control the oxygen feed to thehigh pressure reactor. The gauge has a sufficient range toencompass 0 to 650 kPa or more (; 90 psig) required by thetest method with division 2.0 kPa (; 0.5 psig) or better toenable readings to be made to 2.0 k

26、Pa (; 0.25 psig).7. Reagents7.1 Purity of ReagentsReagent grade chemicals shall beused in all tests. Unless otherwise indicated, it is intended thatall reagents shall conform to the specifications of the Commit-tee onAnalytical Reagents of theAmerican Chemical Society.47.2 Purity of WaterUnless othe

27、rwise indicated, referencesto water shall be understood to mean distilled water meetingrequirements of reagent water as defined by Type I of Speci-fication D1193.7.3 Acetone,CH3COCH3.(WarningExtremely flam-mable. Irritating to skin, eyes, and mucous membranes.)7.4 Air, containing 2000 ppm nitrogen d

28、ioxide, NO2(com-mercially available compressed gas mixture, certified within65 %). (WarningNitrogen dioxide is poisonous.)7.5 Hexane,C6H14, Practical Grade or other suitable hydro-carbon solvent. (WarningExtremely flammable. Harmful ifinhaled. May produce nerve cell damage. Skin irritant onrepeated

29、contact. Aspiration hazard.)7.6 Isopropyl Alcohol,CH3CH(CH3)OH. (WarningFlammable. Eye irritant. Vapors narcotic.)7.7 Oxygen.(WarningOxygen vigorously acceleratescombustion.)7.8 Potassium Hydroxide, Alcohol Solution (1.5 %)Dissolve 12 g of potassium hydroxide (KOH) pellets in 1 L of99 % isopropyl al

30、cohol. (WarningPotassium hydroxide iscorrosive.)8. Materials8.1 Fuel ComponentThe fuel component is an oxidizednitrated gasoline fraction. This component may be prepared inaccordance with the procedures described in Annex A2. (See8.2 and Note 4.) (WarningFuel component is extremelyflammable. Vapors

31、harmful if inhaled. Skin irritant on repeatedcontact. Aspiration hazard.)8.2 Soluble Metal Catalyst MixtureThis catalyst5,6is amixture of soluble metal catalysts (lead, copper, iron, manga-nese, and tin). The catalyst may be prepared according to theprocedures described in Annex A3. (See 8.2 and Not

32、e 4.)(WarningLead and manganese naphthenates are known tobe poisonous, but all naphthenates should be handled with care.Naphthenates are also flammable.)NOTE 4With some catalyst chemicals, reactivity can be a problem.This can be curtailed by storing in a refrigerator at approximately 5C. The4Reagent

33、 Chemicals, American Chemical Society Specifications, AmericanChemical Society, Washington, DC. For Suggestions on the testing of reagents notlisted by the American Chemical Society, see Annual Standards for LaboratoryChemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeiaand Na

34、tional Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.5The sole source of supply of the catalyst known to the committee at this timeis Tannas Co., 4800 James Savage Rd., Midland, MI 48642.6If you are aware of alternative suppliers, please provide this information toASTM Internat

35、ional Headquarters. Your comments will receive careful consider-ation at a meeting of the responsible technical committee,1which you may attend.FIG. 2 Pressure versus Time Diagram of the Oxidation TestFIG. 3 Schematic Drawing of an Assembled Vessel, AluminumInsert, and Glass Sample ContainerD4742 08

36、13catalyst chemicals remain effective up to six months after the septum ispunctured if they are stored as noted above.NOTE 5It is recommended that each new batch of fuel or metalcatalyst be correlated with a standard reference oil, in accordance withgood laboratory practices.8.3 Liquid Detergent (In

37、dustrial Strength).8.4 Silicone Stopcock Grease.9. Preparation of Apparatus9.1 Glass Sample ContainerRinse the glass sample con-tainer with hexane or other suitable hydrocarbon solvent. Cleanthe glass container with hot detergent solution and water. Rinsethe container with acetone. Blow the containe

38、r dry with cleancompressed air.NOTE 6A clean glass sample container is important for obtainingrepeatable results. Thorough cleaning of the glass sample can be accom-plished by (1) hexane rinse, (2) acetone soak for 15 min, (3) hot detergentsolution and water soak for 4 h, (4) acetone rinse, and (5)

39、hexane rinse. Aclean glass sample container is important for obtaining repeatable results.NOTE 7A segmented glass sample container has been found suitableto prevent premature mixing of the catalyst components.9.2 Cleaning of High Pressure ReactorWash the inside ofthe high pressure reactor, aluminum

40、insert, lid, and inside withhot detergent solution and water. Rinse the inside of the stemwith isopropyl alcohol and blow dry with clean compressed air.If the high pressure reactor, insert, lid, or inside of the stememits acidic odor after simple cleaning, wash with 1.5 %alcoholic potassium hydroxid

41、e (KOH) solution, and repeat thecleaning procedures.9.3 Cleaning of High Pressure Reactor StemIt is recom-mended to periodically disassemble, inspect, and clean the highpressure reactor stem. Rinse the inside of the stem withisopropyl alcohol and blow dry with clean compressed air.After cleansing, i

42、t is recommended to insert a dry pipe cleanerinto the transducer line opening for removal of potentialresidue buildup.NOTE 8It is recommended to replace the O-rings when reassemblingthe pressure transducers.9.4 To obtain a representative sample of stocks of uniformpetroleum products, follow Practice

43、 D4057.9.5 Cleaning of Catalyst SyringesIndividual catalyst sy-ringes are to be used for each catalyst component. They are tobe thoroughly cleaned and dried prior to each use. (See AnnexA4 for recommended procedure.)10. Procedure10.1 Weighing and Mixing Sample and Catalyst Compo-nents:10.1.1 Weigh t

44、he clean glass sample container to the nearestmg.10.1.2 Weigh 1.500 6 0.001 g of oil sample into thecontainer.10.1.3 Add 0.060 6 0.001 g each of both the fuel compo-nent and the soluble metal catalyst mixture.10.1.4 Add 0.030 6 0.001 g of distilled water (Type I) to theglass sample container.10.1.5

45、Just prior to inserting the glass sample container intothe high pressure reactor, thoroughly mix the catalyst compo-nents within the sample container by hand-rotation (approxi-mately five rotations) and proceed immediately to 10.2. Delaymay result in variation of results.10.2 High Pressure Reactor C

46、harging and AssemblyImmediately and rapidly assemble the high pressure reactor asshown in Fig. 1.10.2.1 Put the aluminum insert into the high pressurereactor followed by the glass sample container and the TFE(tetra-fluoroethylene) plastic cover disk.10.2.2 Place the stainless hold-down spring on top

47、 of theTFE disk and the glass sample container.NOTE 9The stainless steel hold-down spring not only holds down theTFE cover disk but, more importantly, prevents the glass sample containerfrom slipping inside the high pressure reactor with consequent poorresults.10.2.3 Apply a thin coating of silicone

48、 stopcock grease tothe O-ring high pressure reactor seal located in the gasketgroove of the high pressure reactor lid to provide lubrication.10.2.4 Insert the lid into the high pressure reactor.10.2.5 Place and tighten the cap on the high pressure reactorto lock down the lid in the high pressure rea

49、ctor.10.2.6 Attach the high pressure oxygen hose and purge thehigh pressure reactor twice at about 620 kPa (90 psig) ofoxygen to remove the air originally present in the high pressurereactor.NOTE 10It is advisable to avoid releasing the oxygen too rapidly bydecreasing the pressure to atmospheric in no less than one minute to avoidpossible foaming and overflow of the sample from the glass samplecontainer.10.2.7 Charge the high pressure reactor to 620 kPa (90 psig)oxygen at 21C using an in-line precision pressure gauge tomonitor the high