ASTM D3893-2003(2009) Standard Test Method for Purity of Methyl Amyl Ketone and Methyl Isoamyl Ketone by Gas Chromatography《气相色谱法测定甲基戊基酮和甲基异戊基酮纯度的标准试验方法》.pdf

《ASTM D3893-2003(2009) Standard Test Method for Purity of Methyl Amyl Ketone and Methyl Isoamyl Ketone by Gas Chromatography《气相色谱法测定甲基戊基酮和甲基异戊基酮纯度的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D3893-2003(2009) Standard Test Method for Purity of Methyl Amyl Ketone and Methyl Isoamyl Ketone by Gas Chromatography《气相色谱法测定甲基戊基酮和甲基异戊基酮纯度的标准试验方法》.pdf（5页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D3893 03 (Reapproved 2009)Standard Test Method forPurity of Methyl Amyl Ketone and Methyl Isoamyl Ketone byGas Chromatography1This standard is issued under the fixed designation D3893; the number immediately following the designation indicates the year oforiginal adoption or, in the cas

2、e 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 determination of the purityof methyl amyl ketone and methyl is

3、oamyl ketone. In addition,the method determines total ketones and various impuritieswhich may include acetone, isopropyl alcohol, methyl propylketone, methyl isobutyl ketone, methyl butyl ketone, methylisobutyl carbinol, mesityl oxide, methyl isoamyl ketone, me-thyl butyl carbinol, methyl amyl keton

4、e, and diisobutyl ketone.1.2 Water and acid cannot be determined by this testmethod. They must be determined by other appropriate ASTMprocedures, and the results used to normalize the chromato-graphic data.1.3 For purposes of determining conformance of an ob-served or a calculated value using this t

5、est method to relevantspecifications, test result(s) shall be rounded “off to the nearestunit” in the last right-hand digit used in expressing thespecification limit, in accordance with the rounding-off methodof Practice E29.1.4 The values stated in SI units are to be regarded asstandard. No other u

6、nits of measurement are included in thisstandard.1.5 For hazard information and guidance, see the suppliersMaterial Safety Data Sheet.1.6 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 esta

7、blish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2D1364 Test Method for Water in Volatile Solvents (KarlFischer Reagent Titration Method)D1613 Test Method for Acidity in Volatile Solvents

8、andChemical Intermediates Used in Paint, Varnish, Lacquer,and Related ProductsE29 Practice for Using Significant Digits in Test Data toDetermine Conformance with SpecificationsE180 Practice for Determining the Precision of ASTMMethods for Analysis and Testing of Industrial and Spe-cialty Chemicals33

9、. Summary of Method3.1 A representative specimen is introduced onto a gas-liquid partition column. The separated components are mea-sured in the effluent by a detector and recorded as a chromato-gram. The chromatogram is interpreted by applying componentattenuation and detector response factors to t

10、he peak areas andrelative concentrations are determined by relating the indi-vidual peak responses to the total peak response. Water andacidity are measured by Test Methods D1364 and D1613,respectively, and the results are used to normalize the valuesobtained by gas chromatography.4. Significance an

11、d Use4.1 This procedure is designed to determine the purity of thetwo ketones, methyl isoamyl ketone and methyl amyl ketone,and to obtain the concentration of their various impurities,several of which are critical in the application of these solvents.5. Apparatus5.1 ChromatographAny gas-liquid chrom

12、atographic in-strument having either a thermal conductivity or flame ioniza-tion detector and sufficient sensitivity and stability to obtain for0.01 % impurity in the specimen a recorder deflection of atleast 20 mm at a signal-to-noise ratio of at least 5 to 1. Arecording integrator or computer data

13、 processing system mayalso be used.1This test method is under the jurisdiction of ASTM Committee D01 on Paintand Related Coatings, Materials, and Applications and is the direct responsibility ofSubcommittee D01.35 on Solvents, Plasticizers, and Chemical Intermediates.Current edition approved Dec. 1,

14、 2009. Published December 2009. Originallyapproved in 1980. Last previous edition approved in 2003 as D3893 - 03. DOI:10.1520/D3893-03R09.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume

15、information, refer to the standards Document Summary page onthe ASTM website.3Withdrawn. The last approved version of this historical standard is referencedon www.astm.org.1*A Summary of Changes section appears at the end of this standard.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C

16、700, West Conshohocken, PA 19428-2959, United States.5.1.1 The injection port of the chromatograph must have avolume of at least 1.2 mL to provide for proper vaporization ofthe specimen. The use of a smaller injection port or on-columninjection causes peak broadening and tailing.5.2 ColumnFour and o

17、ne half m of 3.2-mm stainless steeltubing packed with 80 to 90-mesh acid-washed, base-washed,and silanized diatomaceous earth support coated with 10.0 %20 000 molecular weight polyethylene glycol and a 8.33 %phenyl methyl (50:50) silicone. A capillary column, capable ofthe required separation may al

18、so be used.5.3 Specimen Introduction SystemAny system capable ofintroducing a representative specimen onto the column. Micro-liter syringes have been used successfully.5.4 RecorderA recording potentiometer with a full-scaledeflection of 1 mV, full-scale response time of1sorless, andsufficient sensit

19、ivity and stability to meet the requirements of5.1.6. Reagents and Materials6.1 Carrier Gas, appropriate to the type of detector used.Helium or hydrogen may be employed with thermal conduc-tivity detectors and nitrogen, helium, or argon with flameionization detectors. The minimum purity of the carri

20、er gasused should be 99.95 mol %. An oxygen removal system isrecommended for the carrier gas.6.1.1 WarningIf hydrogen is used, take special safetyprecautions to ensure that the system is free of leaks and thatthe effluent is vented properly.6.2 Column Materials:6.2.1 Liquid Phase20 000 molecular wei

21、ght polyethyl-ene glycol and phenyl methyl (50:50) silicone.6.2.2 Solid SupportAcid-washed, base-washed, and si-lanized diatomaceous earth, 80 to 90 mesh.6.2.3 SolventsMethylene chloride, reagent grade.6.2.4 Tubing MaterialThe stainless steel tubing must beof uniform internal diameter and must be cl

22、ean. Wash theinside of the tubing with methylene chloride, then water, andfinally methyl alcohol and blow dry with nitrogen.6.3 Standards for Calibration and IdentificationStandardsamples of all components are needed for establishing identi-fication by retention time and for calibration for quantita

23、tivemeasurements. In most cases, the pure compounds required forcalibration cannot be purchased and must be purified bydistillation before use.7. Preparation of Column7.1 Place 50 g of the solid support, 80 to 90 mesh, in a largeevaporating dish. Dissolve 12.5 g of the polyethylene glycol inabout 40

24、 mL of methylene chloride and add to the solidsupport. Add additional methylene chloride to wet and coverthe solid support. Evaporate the methylene chloride in a fumehood with gentle stirring and under a gentle stream of nitrogen.7.2 Place 50 g of the solid support in a large evaporatingdish. Dissol

25、ve 10 g of the phenyl methyl silicone in about 40mL of methylene chloride and add to the solid support. Addadditional methylene chloride to wet and cover the solidsupport. Evaporate the methylene chloride in a fume hood withgentle stirring and under a gentle stream of nitrogen.7.3 Add 12 g of the pa

26、cking prepared in 7.1 and 12 g of thepacking prepared in 7.2 to a small glass bottle or beaker andmix well. The mixture is used as the column packing material.7.4 Column PreparationThe method used to pack thecolumn is not critical provided that the finished columnproduces the required separation of

27、all of the components to bedetermined.8. Calibration and Standardization8.1 ChromatographInstall the column in the chromato-graph and adjust the operating parameters as directed in Table1. Allow sufficient time for the instrument to reach equilibriumas indicated by a stable recorder baseline.8.2 Det

28、ermine the retention time of each component byinjecting small amounts either separately or in known mix-tures. The components should elute close to the typicalretention times given in Table 1 and the chromatograms shouldclosely approximate those shown in Fig. 1 and Fig. 2.8.3 The area under each pea

29、k of the chromatogram isconsidered a quantitative measure of the corresponding com-pound. The relative area is proportional to concentration if thedetector responds equally to all the sample components. Theresponse to different components is generally significantlydifferent for both flame ionization

30、 and thermal conductivitydetectors. This difference in detector response may be cor-rected by use of relative response factors obtained by injectingand measuring the response of pure components or knownblends. For accurate determination of the impurities, prepareand analyze a known blend containing

31、the impurities inconcentrations that approximate the maximum specificationlimit. Calculate the response factors relative to unity for themajor ketone.9. Procedure9.1 Introduce a representative specimen into the chromato-graph using sufficient material to ensure a minimum 10 %recorder deflection for

32、a 0.1 % concentration of impurity at themost sensitive setting of the instrument.TABLE 1 Instrument Conditions and Retention TimesTemperature, C:Column, isothermal 100Injection port 170Detector block 210Carrier gas HeliumFlow rate, mL/min 25MethylAmylKetoneMethylIsoamylKetoneRelative retention times

33、,major component = 1.00Air 0.04 0.05Acetone 0.14 0.18Isopropyl alcohol 0.18 0.23Methyl propyl ketone 0.31 0.38Methyl isobutyl ketone 0.35 0.45Methyl butyl ketone 0.51 0.64Methyl isobutyl carbinol 0.61 0.77Mesityl oxide 0.65 0.83Methyl isoamyl ketone 0.73 1.00Methyl butyl carbinol 0.82 1.02Methyl amy

34、l ketone 1.00 1.16Diisobutyl ketone 1.04 1.25D3893 03 (2009)2NOTE 1The best separation of the impurities has been obtained withspecimen sizes of 1 or 2 L.9.2 Using the same conditions as for component identifica-tion and standardization, record the peaks of all components atattenuation settings that

35、 provide optimum peak heights.10. Calculation10.1 Measure the area of all peaks (Note 2) and multiplyeach area by the appropriate attenuation factor to express thepeak areas on a common basis. Apply the appropriate detectorresponse to each component to obtain the corrected peakresponse. Calculate th

36、e weight percent composition by divid-ing the individual corrected component areas by the totalcorrected area. Make corrections to account for water andacidity present as determined by the ASTM methods given in2.1.NOTE 2Peak areas may be determined by any method that meets theprecision limits given

37、in Section 12. For best results determine peak areasby electronic integration.10.2 Calculate the weight percent of each component asfollows:Weight % 5AB3 100 2 C! (1)where:A = corrected peak response,B = sum of corrected peak responses, andC = sum of water and acidity in weight percent.10.3 Calculat

38、e the total ketones concentration by summingthe weight percent of all ketones detected.11. Report11.1 Report the total ketone content, purity, and quantity ofthe various impurities to the nearest 0.01 %. Duplicate runs forthe total ketone and purity values that agree within 0.15 %absolute are accept

39、able for averaging (95 % confidence level).Duplicate runs for the impurities that agree within 0.03 %absolute are acceptable for averaging.FIG. 1 Typical Chromatogram of Methyl Amyl KetoneD3893 03 (2009)312. Precision and Bias412.1 PrecisionThe precision statements are based upon aninterlaboratory s

40、tudy in which one operator in five laboratoriesanalyzed in duplicate on two different days one sample of eachof the following ketones of the average composition shown inTable 2. The results were analyzed in accordance with PracticeE180. The within-laboratory and between-laboratories stan-dard deviat

41、ions were found to be as shown in Table 3. Basedupon these standard deviations, the following criteria should beused for judging the acceptability of results at the 95 %confidence level.12.1.1 RepeatabilityTwo results, each the mean of dupli-cates, obtained by the same operator on different days sho

42、uldbe considered suspect if they differ by more than as shown inTable 4.4Supporting data have been filed at ASTM International Headquarters and maybe obtained by requesting Research Report RR: D01-1043.FIG. 2 Typical Chromatogram of Methyl Isoamyl KetoneTABLE 2 Average Compositions of Samples Used i

43、nPrecision DeterminationMethylIsoamylKetone(MIAK)MethylAmylKetone(MAK)Total ketones 99.66 99.76MIAK 99.0 .MAK . 99.11Isopropyl alcohol (IPA) 0.06 0.06Mesityl oxide (MO) 0.12 .Methyl isoamyl carbinol (MIAC) 0.11 .Methyl isobutyl carbinol (MIBC) . 0.04D3893 03 (2009)412.1.2 ReproducibilityTwo results,

44、 each the mean of du-plicates, obtained by operators in different laboratories shouldbe considered suspect if they differ by more than as shown inTable 4.12.2 BiasBias cannot be determined for this test methodbecause there is no available material having an acceptedreference value.13. Keywords13.1 g

45、as chromatography; methyl amyl ketone (MAK);methyl isoamyl ketone (MIAK); purity; solventsSUMMARY OF CHANGESCommittee D01 has identified the location of selected changes to this standard since the last date of issue(D3893 - 99) that may impact the use of this standard.(1)Added reference to Practice

46、E29 in 1.3 of the Scope section. (2) Added Practice E29 to list of Referenced Documents.ASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentionedin this standard. Users of this standard are expressly advised that determination of

47、 the validity of any such patent rights, and the riskof infringement of such rights, are entirely their own responsibility.This standard is subject to revision at any time by the responsible technical committee and must be reviewed every five years andif not revised, either reapproved or withdrawn.

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