ASTM D5827-2009(2015) 8564 Standard Test Method for Analysis of Engine Coolant for Chloride and Other Anions by Ion Chromatography《采用离子色谱法分析氯化物和其它阴离子的发动机冷却剂的标准试验方法》.pdf

《ASTM D5827-2009(2015) 8564 Standard Test Method for Analysis of Engine Coolant for Chloride and Other Anions by Ion Chromatography《采用离子色谱法分析氯化物和其它阴离子的发动机冷却剂的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D5827-2009(2015) 8564 Standard Test Method for Analysis of Engine Coolant for Chloride and Other Anions by Ion Chromatography《采用离子色谱法分析氯化物和其它阴离子的发动机冷却剂的标准试验方法》.pdf（6页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D5827 09 (Reapproved 2015)Standard Test Method forAnalysis of Engine Coolant for Chloride and Other Anionsby Ion Chromatography1This standard is issued under the fixed designation D5827; the number immediately following the designation indicates the year oforiginal adoption or, in the c

2、ase 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.1. Scope*1.1 This test method covers the chemical analysis of enginecoolant for chloride ion by high-

3、performance ion chromatog-raphy (HPIC). Several other common anions found in enginecoolant can be determined in one chromatographic analysis bythis test method.1.2 This test method is applicable to both new and usedengine coolant.1.3 Coelution of other ions may cause interferences for anyof the list

4、ed anions. In the case of unfamiliar formulations,identification verification should be performed by either orboth fortification and dilution of the sample matrix with theanions of interest.1.4 Analysis can be performed directly by this test methodwithout pretreatment, other than dilution, as requir

5、ed by thelinear ranges of the equipment. Table 1 indicates severalapplicable anions and approximate detection limits.1.5 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.6 This standard does not purport to address all of thesaf

6、ety 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 limitations prior to its use.2. Referenced Documents2.1 ASTM Standards:2D1193 Specification for Rea

7、gent WaterD1176 Practice for Sampling and Preparing Aqueous Solu-tions of Engine Coolants orAntirusts for Testing PurposesE691 Practice for Conducting an Interlaboratory Study toDetermine the Precision of a Test MethodE177 Practice for Use of the Terms Precision and Bias inASTM Test Methods3. Summar

8、y of Test Method3.1 A small volume of working sample is prepared bydilution of the sample with the method eluant. This dilutedsample is filtered and pumped through two ion exchangecolumns and a suppressor and into a conductivity detector. Ionsare separated based on their affinity for exchange sites

9、of theresin with respect to the resins affinity for the eluant. Thesuppressor increases the sensitivity of the method by bothincreasing the conductivity of the analytes and decreasing theconductivity of the eluant. The suppressor converts the eluantand the analytes to the corresponding hydrogen form

10、 acids.Anions are quantitated by integration of their response com-pared with an external calibration curve and are reported asmilligrams per litre (mg/L).4. Significance and Use4.1 This test method provides for the qualitative and quan-titative determination of common anions in engine coolant inthe

11、 milligrams per litre to low percent range and requires onlya few millilitres or microlitres of sample per test, with resultsavailable in less than 30 min.Acceptable levels of chloride andother anions vary with manufacturers blending specificationsand applicable ASTM minimum or maximum specification

12、s.5. Interferences5.1 Interferences can be caused by substances with similarretention times, especially if they are in high concentrationcompared to those of the analyte of interest. Sample dilutionwill be used to minimize or solve most interference problems.5.2 A water dip (solvent system peak) can

13、 cause interfer-ence with some integrators. This is eliminated by dilution withthe eluant if the sample dilution factor is 49 + 1 (v/v) or greater.Below this dilution, it is best to add a spike of eluantconcentrate to the sample such that the sample is not dilutedsignificantly and the resulting test

14、 solution matches the eluantused in the system. One method is the addition of 100 L of100X eluant concentrate to 10.0 mL of sample or standard.1This test method is under the jurisdiction of ASTM Committee D15 on EngineCoolants and Related Fluids and is the direct responsibility of SubcommitteeD15.04

15、 on Chemical Properties.Current edition approved May 1, 2015. Published June 2015. Originallyapproved in 1995. Last previous edition approved in 2009 as D5827-091. DOI:10.1520/D5827-09R15.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at service

16、astm.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 19428-2959. United S

17、tates15.3 Method interferences can be caused by the contamina-tion of glassware, eluant, reagents, etc. Great care must betaken to ensure that contamination, especially by chloride, iskept at the lowest possible levels.5.4 Pre-rinsing of the sample preparation containers withdeionized water is manda

18、tory.5.5 The use of latex gloves is highly recommended toprevent contamination.6. Apparatus6.1 Analytical Balance, capable of weighing accurately to0.0001 g.6.2 Ion ChromatographAnalytical system with all re-quired accessories including syringes, columns, suppressor,gasses, and detector. Column life

19、 and performance are en-hanced by the use of a two-eluant channel gradient pump, ifavailable.6.3 Guard Column, for protection of the analytical columnfrom strongly retained constituents. Better separations areobtained with additional plates.6.4 Anion Separator Column, capable of producing analytesep

20、aration equivalent to or better than that shown in Fig. 1.6.5 Anion Suppressor DeviceMicro membrane suppressoror equivalent. A cation exchange column in the hydrogen formhas been used successfully, but it will periodically need to beregenerated as required, being indicated by a high backgroundconduc

21、tivity and low analyte response.6.6 Conductivity Detector, low volume (2 L) and flow,temperature compensated, capable of at least 0 to 1000 S/cmon a linear scale.6.7 Integrator or Chromatography Data System Software,capable of obtaining approximately the same detection limitsas are listed in Table 1

22、.6.8 Drying Oven, controlled at 105, 150, and 600 6 5C.6.9 Desiccator.7. Reagents7.1 Purity of ReagentsReagent grade or higher puritychemicals shall be used for the preparation of all samples,standards, eluants, and regenerator solutions. Unless otherwiseindicated, it is intended that all reagents c

23、onform to thespecifications of the Committee on Analytical Reagents of theAmerican Chemical Society, where such specification areavailable.3Other grades may be used, provided it is firstascertained that the reagent is of sufficiently high purity topermit its use without lessening the accuracy of the

24、 determi-nation.7.2 Purity of WaterUnless otherwise indicated, referencesto water shall be understood to mean reagent water as definedby Type II of Specification D1193. It is recommended that allwater be filtered through a 0.2-m filter. For eluant preparation,degas the water by sparging with helium

25、or vacuum degassingand sonication.7.3 Eluant Buffer Stock SolutionSodium bicarbonate(NaHCO3) 1.5 mM and sodium carbonate (Na2CO3) 1.2 mM.Dissolve 2.5203 6 0.0005 g of NaHCO3and 2.5438 6 0.0005gofNa2CO3in reagent water in a 1000-mLTypeAvolumetricflask and dilute to 1 L. Dilute 100.0 mL of this stock

26、solutionto 2000 mL in a 2-L Type A volumetric flask with degassedreagent water. The pH of the stock solution is 10.1 to 10.3(based on pKacalculation). The eluant solution used may bedifferent if other system or analytical columns are used.7.4 Stock Bromide SolutionDry approximately2gofsodium bromide

27、 (NaBr) for6hat150C and cool in adesiccator. Weigh and dissolve 1.2877 g of the dried salt inreagent water and dilute to 1 L (1.00 mL = 1.00 mg bromide).3Reagent Chemicals, American Chemical Society Specifications, AmericanChemical Society, Washington, DC. For suggestions on the testing of reagents

28、notlisted by the American Chemical Society, see Analar Standards for LaboratoryChemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeiaand National Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.TABLE 1 Analytes and Minimum Detection LimitsAnalyte Detection L

29、imit, mg/LAChloride (Cl)2.0Nitrite (NO2)5Bromide (Br) 4.0Nitrate (NO3)71o-Phosphate (HPO4)220.0Sulfate (SO4)28.0Oxalate (C2O4)212.0ADetermined using 100-L sample volume. Sample diluted 99 + 1 (v/v) withchromatographic eluant 30-S/cm full scale, suppressed conductivity detection.Dionex AS4ASC column

30、with AG4ASC guard columns. Other systems will requireMDL determinations using chosen dilution factors, eluants, columns, and detector.FIG. 1 Sample RunChloride Peak at 1.7 minD5827 09 (2015)27.5 Stock Chloride SolutionDry approximately2gofsodium chloride (NaCl) for1hat600C and cool in adesiccator. W

31、eigh and dissolve 1.6485 g and dilute to 1 L withreagent water (1.00 mL = 1.00 mg Cl).7.6 Stock Formate SolutionDry approximately2gofsodium formate (NaHCO2) at 105C for 6 h and cool in adesiccator. Weigh and dissolve 1.4775 g of the salt in reagentwater and dilute to 1 L (1.00 mL = 1.00 mg formic ac

32、id).7.7 Stock Glycolic Acid SolutionWeigh and dissolve1.0000 g of the solid acid in reagent water and dilute to 1 L(1.00 mL = 1.00 mg glycolate).7.8 Stock Nitrate SolutionDry approximately2gofso-dium nitrate (NaNO3) for 24 h at 105C and cool in adesiccator. Weigh and dissolve 1.3707 g and dilute to

33、1 L withreagent water (1.00 mL = 1.00 mg NO3).7.9 Stock Nitrite SolutionDry approximately2gofso-dium nitrite (NaNO2) for 24 h in a desiccator containingconcentrated sulfuric acid (relative density of 1.84). Weigh anddissolve 1.4998 g and dilute to 1 L with reagent water (1.00mL = 1.00 mg NO2). Refri

34、gerate and prepare weekly becausenitrite is oxidized easily.7.10 Stock Oxalic Acid SolutionWeigh and dissolve1.4002 g of oxalic acid dihydrate (C2H2O42H2O) in reagentwater and dilute to 1 L (1.00 mL = 1.00 mg oxalic acid).7.11 Stock Phosphate SolutionWeigh and dissolve 1.4330g of potassium dihydroge

35、n phosphate (KH2PO4) and dilute to1 L with reagent water (1.00 mL = 1.00 mg PO43).7.12 Stock Sulfate SolutionDry approximately2gofanhydrous sodium sulfate (Na2SO4)for1hat105C and coolin a desiccator. Weigh and dissolve 1.4790 g and dilute to 1 Lwith reagent water (1.00 mL = 1.00 mg SO42).7.13 Suppre

36、ssor Solution for Membrane Suppressor0.025N H2SO4. Carefully add 13.7 mL of reagent sulfuric acid(relative density of 1.84) to approximately 500 mL reagentwater in a 1-Lvolumetric flask. Dilute to 1000 mLwith reagentwater. Dilute 100 mL of this concentrate to 2000 mL withreagent water for the final

37、working suppressor solution.7.14 StabilityStandard stock solutions are stable for atleast one month when stored at 4C. Fresh nitrite and phos-phate standards must be prepared weekly.8. Sampling8.1 Collect the sample in a scrupulously clean glass orpolyethylene bottle in accordance with Practice D117

38、6. Collectat least 100 mL of sample.9. Calibration and Standardization9.1 Analyze each standard solution separately to determinethe analytes retention time.9.2 Set the chromatograph up in accordance with the con-ditions specified in Table 2 and Fig. 2. The use of otherequipment, eluants, or flows re

39、quires calculation of suitabledilution factors and instrument settings that permit the analystto obtain the resolution and detection limits given in Fig. 1 andTable 1, respectively.9.3 Prepare concentrations of chloride at 0.08, 0.4, 0.8, and4.0 mg/L from the stock solution. All final solutions shou

40、ld bemade with eluant as described in 5.2. Calibrate the ionchromatograph with at least five levels of the analyte, startingnear but above the minimum detection limit (MDL) and furtherdefining the working range in samples subsequent to dilution.These chloride analyte examples reflect a dilution of 9

41、9 + 1(v/v) with eluant. If it is desirable to calibrate for another anionspecies, these may be combined in the preceding five calibra-tion standards once the retention times have been establishedindividually. Concentrations of these other anions in thecalibration solutions must bracket the expected

42、range for thesespecies and include a level near the MDL for each species.NOTE 1Ion chromatography equipment other than that described inthis test method may require that standards be prepared at higher or lowerlevels.9.4 Analyze a blank containing only the eluant as describedin Section 10.9.5 A mid-

43、range standard must be used to verify theresolution of anions, regardless of a desire to quantitate all ofthem.9.6 Analytical curves must be established at only onedetector scale setting in order to prevent a change of slopeaffecting the analytical curve.9.7 The analytical calibration curve and an e

44、luant blankshall be verified daily prior to the analysis of samples to verifythe system resolution, calibration, and sensitivity.9.8 The analytical calibration curve, analyte retention timesand resolution, and an eluant blank shall be verified subsequentto a change of the system eluant.9.9 Condition

45、s:Column: ion chromatography Flow: 2 mL/minDetector: see 6.6 Suppressor flow: 2 mL/minEluant: see 7.3 Sample loop: 50 LNOTE 2If a gradient pump is available, refer to Fig. 2 for an exampleof a step gradient that has proven successful for cleaning the column ofstrongly retained species such as polyph

46、osphates and molybdate, whichwould otherwise elute in subsequent runs.NOTE 3The sample loop volume will vary based on the columncapacity, sensitivity, and other factors. Refer to ion chromatographyequipment manuals and column information for machine-specific details.10. Procedure10.1 Set the ion chr

47、omatograph up in accordance with themanufacturers instructions.TABLE 2 Chromatographic ConditionsAnalyte Peak No. Retention Time, minChloride 2A1.7Nitrite 3 2.1Bromide 4 3.3Nitrate 5 3.7Phosphate 6 7.7Sulfate 7 10.5Oxalate 8 13.3AFluoride, acetate, formate, and glycolate will all elute before chlori

48、de, and poorresolution of these species often precludes the quantitation of any, or all four, ofthem.D5827 09 (2015)310.2 Equilibrate the system by pumping eluant for 15 to 30min, until a stable baseline is obtained. Sample preparation isusually performed by 99 + 1 (v/v) dilution with eluant.10.3 Fl

49、ush the injection loop with 2 to 3 mLof sample usinga 10-mL disposable plastic syringe fitted with a 0.2-m syringefilter.410.4 Start the chromatographic run in accordance with themanufacturers instructions.10.5 At least one duplicate and one fortified coolant samplemust be analyzed with each batch of ten or fewer samples.Results must be recorded in the laboratory manual. Thefortified sample is to be prepared by addition of a mixedanalyte mid-range standard. Addition of 100 L of fortificationstandard solution to 10 mL of prepared