ASTM D4628-2005(2011)e1 Standard Test Method for Analysis of Barium Calcium Magnesium and Zinc in Unused Lubricating Oils by Atomic Absorption Spectrometry《原子吸收光谱法分析未用的润滑油中钡 钙 镁和锌的.pdf

《ASTM D4628-2005(2011)e1 Standard Test Method for Analysis of Barium Calcium Magnesium and Zinc in Unused Lubricating Oils by Atomic Absorption Spectrometry《原子吸收光谱法分析未用的润滑油中钡 钙 镁和锌的.pdf》由会员分享，可在线阅读，更多相关《ASTM D4628-2005(2011)e1 Standard Test Method for Analysis of Barium Calcium Magnesium and Zinc in Unused Lubricating Oils by Atomic Absorption Spectrometry《原子吸收光谱法分析未用的润滑油中钡 钙 镁和锌的.pdf（7页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D4628 05 (Reapproved 2011)1Standard Test Method forAnalysis of Barium, Calcium, Magnesium, and Zinc inUnused Lubricating Oils by Atomic AbsorptionSpectrometry1This standard is issued under the fixed designation D4628; the number immediately following the designation indicates the year o

2、foriginal adoption or, in the 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 Department

3、of Defense.1NOTEUpdated units statement and added research report number editorially in August 2011.1. Scope1.1 This test method is applicable for the determination ofmass percent barium from 0.005 to 1.0 %, calcium andmagnesium from 0.002 to 0.3 %, and zinc from 0.002 to 0.2 %in lubricating oils.1.

4、2 Higher concentrations can be determined by appropriatedilution. Lower concentrations of metals such as barium,calcium, magnesium, and zinc at about 10 ppm level can alsobe determined by this test method. Use of this test method forthe determination at these lower concentrations should be byagreeme

5、nt between the buyer and the seller.1.3 Lubricating oils that contain viscosity index improversmay give low results when calibrations are performed usingstandards that do not contain viscosity index improvers.1.4 The values stated in SI units are to be regarded asstandard. No other units of measurem

6、ent are included in thisstandard.1.5 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 regulatory limitat

7、ions prior to use. Specific warningstatements are given in 3.1, 6.3, and 8.1.2. Referenced Documents2.1 ASTM Standards:2D6299 Practice for Applying Statistical Quality Assuranceand Control Charting Techniques to Evaluate AnalyticalMeasurement System Performance3. Summary of Test Method3.1 A sample i

8、s weighed and base oil is added to 0.25 60.01-g total mass. Fifty millilitres of a kerosine solution,containing potassium as an ionization suppressant, are added,and the sample and oil are dissolved. (WarningHazardous.Potentially toxic and explosive.) Standards are similarly pre-pared, always adding

9、 oil if necessary to yield a total mass of0.25 g. These solutions are burned in the flame of an atomicabsorption spectrophotometer. An acetylene/nitrous oxideflame is used. (WarningCombustible. Vapor harmful.)4. Significance and Use4.1 Some oils are formulated with metal-containing addi-tives that a

10、ct as detergents, antioxidants, antiwear agents, etc.Some of these additives contain one or more of these metals:barium, calcium, zinc, and magnesium. This test methodprovides a means of determining the concentration of thesemetals that gives an indication of the additive content in theseoils.1This

11、test method is under the jurisdiction of ASTM Committee D02 onPetroleum Products and Lubricants and is the direct responsibility of SubcommitteeD02.03 on Elemental Analysis.Current edition approved May 1, 2011. Published August 2011. Originallyapproved in 1986. Last previous edition approved in 2005

12、 as D462805. DOI:10.1520/D4628-05R11E01.2For 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 onthe ASTM website.1Copyright ASTM Inter

13、national, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.5. Apparatus5.1 Atomic Absorption Spectrophotometer.5.2 Analytical Balance.5.3 Automatic Measuring Pipet or Volumetric Class A Pipet,50-mL capacity.5.4 Bottles with Screw Caps,60mL.NOTE 1Suitable volumetric

14、 flasks or plastic bottles may be substi-tuted.5.5 Shaker, Mechanical Stirrer, or Ultrasonic Bath, capableof handling 60-mL bottles.6. Reagents6.1 Base Oil, metal-free, with a viscosity of about 4 cSt at100C. A100 neutral oil which provides good solvency forstandards and additive concentrate is sati

15、sfactory. Highlyparaffinic oils should be avoided.6.2 2-Ethyl HexanoicAcid, which has been determined to befree of interfering metals.6.3 Kerosine, Metal-FreeSee Notes 2-4.(WarningCombustible. Vapor harmful.) Distillation range from 170C to280C at 100 kPa (1 atm). When the kerosine solvent iscontami

16、nated, it may be purified metal-free by running throughattapulgus clay.NOTE 2Solvents other than kerosine, such as xylene MEK and soforth, may be used in this test method, however, the precision data quotedin Section 16 was obtained using kerosine.NOTE 3Metal-free kerosine can be obtained from most

17、laboratorysupply houses, but should be tested for metal content before using.NOTE 4Satisfactory results have been obtained in this test method byusing Baker “kerosine” (deodorized) which has typical initial and endboiling points of 191C and 240C, respectively, and a typical composi-tion of 96.7 volu

18、me % saturates, 0.1 volume % olefins, and a maximumof 3.2 volume % aromatics. If the kerosine used by an operator deviatesappreciably from this composition, there may be significant error.6.4 Oil-Soluble Metal Compounds,3stock standard blend inbase oil. A 0.25 6 0.01-g portion of this stock standard

19、 blenddiluted with 50 mL of the potassium ionization suppressantsolution (see 6.5) shall yield a reading of 0.5 6 0.1 absorbanceunits for each of the elements barium, calcium, magnesium,and zinc using a minimum of scale expansion or burnerrotation. The concentrations of the metal should be blendedac

20、curately to three significant figures. The actual concentra-tions should be chosen to conform to the optimum workingrange of the particular instrument being used, but as a guideone cooperator used 0.4 % barium, 0.03 % calcium, 0.03 %magnesium, and 0.06 % zinc. The stock standard blend shouldbe heate

21、d and stirred to ensure a homogeneous solution.NOTE 5In addition to the calibration standards identified in 6.4,single-element or multielement calibration standards may also be preparedfrom materials similar to the samples being analyzed, provided thecalibration standards to be used have previously

22、been characterized byindependent, primary (for example, gravimetric or volumetric), andanalytical techniques to establish the elemental concentration masspercent levels.6.5 Potassium Ionization Suppressant Solutioncontainingan oil-soluble potassium compound in kerosine at 2.0 6 0.1 gpotassium/litre

23、of solution.NOTE 6The actual potassium concentration needed varies with thesource of potassium and perhaps the instrumental conditions as well. Todetermine the needed concentration, atomize solutions containing 0, 500,3Oil soluble metal compounds found satisfactory for this test method areavailable

24、from National Institute of Standards and Technology, Office of StandardReference Materials, Washington, DC 20234.FIG. 1 Plot Graphs for Barium and CalciumD4628 05 (2011)121000, 1500, 2000, 2500, and 3000 ppm potassium with 25 ppm bariumand 5 ppm calcium in each. Plot graphs of barium and calcium abs

25、orbanceversus potassium concentration as shown in Fig. 1. The minimumconcentration of potassium needed is that above the knee for both thebarium and calcium curves.6.6 Working StandardsFreshly prepared by weighing intosix 60-mL bottles (1) 0.25, (2) 0.20, (3) 0.15, (4) 0.10, (5) 0.05,and (6)0gofstoc

26、k standard blend (see 6.4) to three significantfigures and add 0.0, 0.05, 0.10, 0.15, 0.20, and 0.25 6 0.01 gof base oil, respectively. Add 50 mL of potassium ionizationsuppressant solution (see 6.5) to each bottle and shake or stir todissolve.NOTE 7Many modern AAS instruments can store up to 3 or 4

27、calibration standards in memory. In such cases, follow the manufacturersinstructions, ensuring that the unknown samples absorbance is in thelinear part of the calibration range used.6.7 Quality Control (QC) Samples, preferably are portionsof one or more liquid petroleum materials that are stable and

28、representative of the samples of interest. These QC samplescan be used to check the validity of the testing process asdescribed in Section 16.7. Sampling7.1 Shake the sample thoroughly before sampling to ensureobtaining a representative sample.8. Preparation of Apparatus8.1 Consult the manufacturers

29、 instructions for the opera-tion of the atomic absorption spectrophotometer. The presenttest method assumes that good operating procedures arefollowed. Design differences between spectrophotometersmake it impractical to specify the required manipulations indetail here. (WarningProper operating proce

30、dures are re-quired for safety as well as for reliability of results. Anexplosion can result from flame blow-back unless the correctburner head and operating sequence are used.)8.2 For the barium determination, fit the barium hollowcathode lamp and set the monochromator at 553.6 nm. Makefine adjustm

31、ents to the wavelength setting to give maximumoutput. Using the correct burner head for acetylene/nitrousoxide, set up the acetylene/nitrous oxide flame. On instrumentswhere applicable, adjust the gain control to set this maximumat full scale, when aspirating standard (6)in6.6.8.3 Aspirate at about

32、2.5 to 3 mL/min a standard bariumsolution into the flame. Make adjustments to the height andangle of the burner and to the acetylene flow rate to givemaximum absorption. Make sure that standard (6)in6.6 stillgives zero absorbance by making adjustments, if necessary.9. Calibration (Barium)9.1 Aspirat

33、e standard (1)in6.6. With a minimum of scaleexpansion or burner rotation, obtain a reading of 0.5 6 0.1 onthe absorbance meter or alternative readout device.9.2 Aspirate the standards of 6.6 sequentially into the flameand record the output (or note the meter deflections). Aspiratethe solvent alone a

34、fter each standard.9.3 Determine the net absorbance of each standard. If thespectrophotometer output is linear in absorbance, the netabsorbance is given by the difference between the absorbancefor the standard or sample solution and the absorbance for thesolvent alone. If the spectrophotometer outpu

35、t is proportionalto transmission (that is, to light intensity) then the net absor-bance is given by log10d0/d1, where the deflections are d0when solvent alone is aspirated and d1when the standard orsample solution is aspirated.9.4 Plot the net absorbance against the concentration (mg/50mL suppressan

36、t solution) of barium in the standards to give acalibration curve.NOTE 8The calibration curve may be automatically calculated by theinstrument software and displayed by way of the instrument computerterminal, making actual plotting unnecessary.9.5 Calibration must be carried out prior to each group

37、ofsamples to be analyzed and after any change in instrumentalconditions, as variation occurs in the instrument behavior.Readings may also vary over short times from such causes asbuildup of deposits on the burner slot or in the nebulizer. Thus,a single standard should be aspirated from time to time

38、duringa series of samples to check whether the calibration haschanged (a check after every fifth sample is recommended).The visual appearance of the flame also serves as a usefulcheck to detect changes of condition.9.6 Determine the slope and intercept for barium based onthe calibration curve develo

39、ped. The values will be used todetermine barium concentrations of samples to be tested.Ensure that the regression coefficient is at least 0.99 for barium,otherwise the laboratory needs to re-calibrate for barium whenthis criteria is not satisfied.10. Procedure (Barium)10.1 Weigh the sample to three

40、significant figures into a60-mLbottle. The sample mass is chosen to give an absorbancereading of 0.2 to 0.5. Add base oil to make 0.25 6 0.01 g totalmass. Add 50 mL of potassium suppressant solution, see 6.5,and dissolve. The maximum sample size to be used is 0.25 g,and the minimum is 0.05 g.10.1.1

41、To hazy samples add 0.25 6 0.01 mL of 2-ethylhexanoic acid and shake. If this clears up the haze, the analysisis run, and the dilution error is corrected by multiplying thefound results by 1.005. If the sample remains hazy, the sampleis not suitable to be analyzed by this test method.10.2 Samples yi

42、elding absorbances greater than 0.5 evenwith the minimum sample size can be accurately diluted withnew base oil to a suitable concentration. Make sure the newsolution is homogeneous before proceeding as instructed in10.1.10.3 Aspirate the sample solution and determine the absor-bance, aspirating sol

43、vent alone before and after each reading.11. Calculation (Barium)11.1 Read from the calibration curve the concentration, C,corresponding to the measured absorbance.C = concentration of barium in the diluted sample solution,mg/50 mL of suppressant solution.11.2 Calculate the barium content of the oil

44、s in percent massas follows:D4628 05 (2011)13Barium, % mass 5CD10W(1)where:W = grams of sample/50 mL,C = milligrams of metal/50 mL, andD = dilution factor if dilution was necessary in 10.2.NOTE 9If the calibration curve is linear, the concentration may bedetermined by an equation instead of a calibr

45、ation curve.12. Calcium Determination12.1 Repeat Sections 7 through 10 replacing referencesmade to barium with calcium using the following conditions:12.1.1 Acetylene/nitrous oxide flame,12.1.2 Calcium hollow cathode lamp, and12.1.3 Analytical line 422.7 nm.13. Magnesium Determination13.1 Repeat Sec

46、tions 7 through 10 replacing referencesmade to barium with magnesium using the following condi-tions:13.1.1 Acetylene/nitrous oxide flame,13.1.2 Magnesium hollow cathode lamp, and13.1.3 Analytical line 285.2 nm.14. Zinc Determination14.1 Repeat Sections 7 through 10 replacing referencesmade to bariu

47、m with zinc using the following conditions:14.1.1 Acetylene/nitrous oxide flame,14.1.2 Zinc hollow cathode lamp, and14.1.3 Analytical line 213.9 nm.NOTE 10Although this test method has been described for thedetermination of four elements on a single sample, the sequence ofoperations in analyzing sev

48、eral samples should also be considered.Aspiration of a sample to determine its absorbance is very quick.Changing wavelength setting and lamps takes longer. Thus, it is mosteconomical to make measurements at a single wavelength on a series ofsamples and standards before changing conditions.15. Report

49、15.1 Report concentrations greater than 0.1 % to threesignificant figures.15.2 Concentrations between 0.0050.1 % barium and0.0020.1 % zinc, calcium, and magnesium are reported to twosignificant figures.15.3 Concentrations less than the lower limits in 15.2 shallbe reported as less than the appropriate lower limit.16. Quality Control16.1 Confirm the performance of the instrument or the testprocedure by analyzing a quality control (QC) sample (see6.7).16.1.1 When QC/Quality Assurance (QA) protocols arealready established in the testing facility, these