ASTM E611-2008(2015) 5083 Standard Test Methods for Low Concentrations of Diethlyene Glycol in Ethylene Glycol by Gas Chromatography《采用气相色谱法测定乙烯中低浓度二甘醇的标准试验方法》.pdf

《ASTM E611-2008(2015) 5083 Standard Test Methods for Low Concentrations of Diethlyene Glycol in Ethylene Glycol by Gas Chromatography《采用气相色谱法测定乙烯中低浓度二甘醇的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM E611-2008(2015) 5083 Standard Test Methods for Low Concentrations of Diethlyene Glycol in Ethylene Glycol by Gas Chromatography《采用气相色谱法测定乙烯中低浓度二甘醇的标准试验方法》.pdf（8页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: E611 08 (Reapproved 2015)Standard Test Methods forLow Concentrations of Diethlyene Glycol in Ethylene Glycolby Gas Chromatography1This standard is issued under the fixed designation E611; the number immediately following the designation indicates the year oforiginal adoption or, in the

2、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.1. Scope*1.1 These test methods are intended primarily for theanalysis of mixtures of ethylene and d

3、iethylene glycols inwhich the diethylene glycol concentration is 0.1 % or less.Both test methods should be applicable to higher concentra-tions of diethylene glycol, but precision and bias estimateshave been obtained only for 0.05 to 0.1 % diethylene glycol.NOTE 1Test Methods E202 describe another g

4、as chromatographic testmethod applicable to mixtures of ethylene, diethylene, and triethyleneglycols and mixtures of propylene, dipropylene, and tripropylene glycolsin which one of the glycols is the principal component and the other twoare present in concentrations of 0.1 to 1 % each.NOTE 2Test Met

5、hod E2409 describes another gas chromatographictest method for the determination of glycol impurities in mono-, di-, tri-and tetraethylene glycol (MEG, DEG, TEG and TeEG) in the range of 5to 3000 g/g.1.2 The two test methods are given as follows:SectionsTest Method ANonderivative Method 5 to 13Test

6、Method BDerivative Method 14 to 221.3 Review the current Material Safety Data Sheets (MSDS)for detailed information concerning toxicity, first aidprocedures, and safety precautions for chemicals used in thisstandard.1.4 The values stated in SI units are to be regarded asstandard. No other units of m

7、easurement are included in thisstandard with the exception of foot-pound units for apparatusdescriptions.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

8、 health practices and determine the applica-bility of regulatory limitations prior to use. For a specificwarning statement, see 15.1.5.2. Referenced Documents2.1 ASTM Standards:2D1193 Specification for Reagent WaterE180 Practice for Determining the Precision of ASTMMethods for Analysis and Testing o

9、f Industrial and Spe-cialty Chemicals (Withdrawn 2009)3E202 Test Methods for Analysis of Ethylene Glycols andPropylene GlycolsE2409 Test Method for Glycol Impurities in Mono-, Di-, Tri-and Tetraethylene Glycol and in Mono- and DipropyleneGlycol(Gas Chromatographic Method)2.2 Other Document:Manufactu

10、rers instruction manuals of gas chromatograph3. Significance and Use3.1 Either test method may be used to determine theconcentrations of diethylene glycol in ethylene glycol. Theconcentrations of the components are obtained by a normal-ization technique, based on the assumption that all componentsar

11、e eluted under the conditions used. If all components shouldnot be eluted, the calculated concentrations will be erroneouslyhigh, with the major component showing the most significantabsolute error. Since water is not detected by these procedures,the results are on a water-free basis. Water may be d

12、eterminedin accordance with the applicable sections of Test MethodsE202 and the gas chromatographic results corrected for thewater concentration.3.2 Both test methods are currently in industrial use. TestMethodAis the simpler of the two test methods because it doesnot require the preparation of deri

13、vatives prior to gas chro-matographic analysis. The results obtained by Test Method Aare slightly more accurate than those obtained by Test MethodB. With respect to precision there is no significant differencebetween the two test methods. Test Method B has beenreported to be suitable also for the an

14、alysis of a wide variety ofglycol ethers, but this use is beyond the scope of this standard.1These test methods are under the jurisdiction of ASTM Committee E15 onIndustrial and Specialty Chemicalsand are the direct responsibility of SubcommitteeE15.02 on Product Standards.Current edition approved J

15、une 1, 2015. Published June 2015. Originallyapproved in 1977. Last previous edition approved in 2008 as E61108. DOI:10.1520/E0611-08R15.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume in

16、formation, refer to the standards Document Summary page onthe ASTM website.3The last approved version of this historical standard is referenced onwww.astm.org.*A Summary of Changes section appears at the end of this standardCopyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Consh

17、ohocken, PA 19428-2959. United States14. Purity of Reagents4.1 Reagent grade chemicals shall be used in all tests.Unless otherwise indicated, it is intended that all reagents shallconform to the specifications of the Committee on AnalyticalReagents of the American Chemical Society, where suchspecifi

18、cations are available.4Other grades may be used, pro-vided it is first ascertained that the reagent is of sufficientlyhigh purity to permit its use without lessening the accuracy ofthe determination.4.2 Unless otherwise indicated, references to water shall beunderstood to mean Type II or III reagent

19、 water conforming toSpecification D1193.TEST METHOD ANONDERIVATIVE METHOD5. Summary of Test Method5.1 The sample is injected into a gas chromatographiccolumn. The components are separated as they pass throughthe column with helium carrier gas, their presence in theeffluent is detected by a flame ion

20、ization detector, and recordedas a chromatogram. The areas under the peaks due to thesample components are corrected by applying appropriatecalibration factors to obtain the composition of the sample ona weight percentage basis.6. Apparatus6.1 Gas Chromatographic Instrument having the followingminim

21、al characteristics (see Table 1).6.1.1 Sample Injection Port, with heater characteristicsnecessary for operation at 210C.6.1.2 Column Oven, capable of isothermal operation at168C.6.1.3 Detector, of conventional flame ionization type, ca-pable of operating at 168C. A conventional thermal conduc-tivit

22、y detector can be used, but sensitivity will be reduced andwater may be detected as a peak eluting with the pressure peakdue to sample injection, depending upon the concentration ofwater. The precision and bias statements in Section 13 are forflame ionization detectors.6.1.4 Recorder, 0 to 1-mV rang

23、e, that 1-s full scale deflec-tion with a chart speed of approximately 1.3 cm/min or otherconvenient speed that will produce a satisfactorychromatogram, and an attenuator switch to change the recorderrange as required to keep the chromatogram on scale.NOTE 3On instruments using electronic integratio

24、n the attenuationfeature is not required.6.1.5 Column, 50 in. long,316 in. in outside diameter with awall thickness of 0.030 in. for copper or 0.020 in. for stainlesssteel construction; packed with 10 % polyethylene glycol onorange calcinated diatomite with dimethyldichlorosilane,DMCS, 60/80 mesh.6.

25、1.6 Microsyringe, 10-L capacity.6.1.7 Copper or Stainless Steel Tubing,316 in. in outsidediameter with a wall thickness of 0.030 in. for copper or 0.020in. for stainless steel.NOTE 4The copper tubing should be sealed, refrigeration grade. If theseal has been broken, clean the copper tubing with an a

26、cetone wash anddry with nitrogen before filling. Stainless steel tubing should be pre-washed with successive volumes of 10 % HCl, distilled water, acetone,methylene chloride, and dried with nitrogen.7. Reagents and Materials7.1 Air, compressed.7.2 Orange Calcinated Diatomite withDimethyldichlorosila

27、ne, 60/80 mesh.7.3 Ethylene Glycol and Diethylene GlycolSee Section 9for purity requirements.7.4 Helium (He).7.5 Hydrogen (H2).7.6 Methylene Chloride (Dichloromethane) (CH2Cl2).7.7 Polyethylene Glycol, 20 000 molecular weight.8. Preparation of Chromatographic Column8.1 Dissolve 20 g of the polyethyl

28、ene glycol in approxi-mately 200 mL of CH2Cl2with gentle warming to aid solution.Add 180 g of orange calcinated diatamite withdimethyldichlorosilane, DMCS, and sufficient CH2Cl2to form4Reagent Chemicals, American Chemical Society Specifications, Am. ChemicalSoc., Washington, DC. For suggestions on t

29、he testing of reagents not listed by theAmerican Chemical Society, see Analar Standards for Laboratory Chemicals, BDHLtd., Poole, Dorset, U.K., and the United States Pharmacopeia and NationalFormulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville, MD.TABLE 1 Instrument Parameters, Method AN

30、onderivativeInstrument Varian Aerograph. Model 204, equipped with flame ionization detectorsAStrip-chart recorder 0-1 mV rangeChart speed12 in. (12.7 mm)/minColumn 50 in. (1270 mm) of316-in. (4.8-mm) outside diameter copper orstainless steel tubing packed with 10 % polyethylene glycol.20 000 molecul

31、ar weight, on Chromosorb G, DMCS, 60/80 meshColumn temperature 168CCarrier gas helium at 100 mL/minHydrogen flow rate 40 mL/minAir flow rate 400 mL/minInjection port temperature 210CDetector block temperature 168CSample size 2LInjection time 28 sAThe parameters in this table apply to a Varian Aerogr

32、aph, Model 204, manufactured by Varian Div., 611 Hansen Way, Palo Alto, CA 94303. Any similar instrument maybe used for this method with appropriate modifications of the parameters.E611 08 (2015)2a slurry, and mix well, making certain that all particles arewetted. Evaporate the CH2Cl2by heating gent

33、ly over a steambath in a fume hood until the mixture is dry. Frequent stirringof the slurry during the drying operation is necessary to obtaina uniform coating. The use of a vacuum rotary evaporator willshorten the time required for drying.8.2 Screen the dried packing through a 50-mesh (300-mscreen

34、opening) and an 80-mesh (180-m screen opening)screen to remove any lumps and fines. Fill a 127-cm section1.4-cm outside diameter copper or stainless steel tubing withthe screened packing retained on the 80-mesh screen. Gentlyvibrate the tubing during packing to ensure uniform packing.Use borosilicat

35、e glass wool for plugs in the ends of the column.Columns packed using vacuum or by blowing the packing intothe tubing are generally unsatisfactory.8.3 Condition the column prior to use by placing the columnin the chromatograph in accordance with 10.1, but do notconnect the column to the detector. Pa

36、ss helium through thecolumn at 100 mL/min during the conditioning.9. Calibration Factors9.1 In order to obtain the composition of the sample in termsof mass percent, multiply the areas associated with the com-ponents by an appropriate calibration factor. These factors areobtained from mixtures of kn

37、own composition, and should bedetermined for each apparatus. The calibration factors may beobtained using standards prepared from “hearts cuts” from thedistillation of each of the glycols, or from commercial gradesof each glycol as described in the following test methods. Forhighest accuracy, use gl

38、ycols obtained from “hearts cuts.”Check the calibration factors periodically or whenever there isevidence of a change in the column or instrument.9.2 Calibration Method 1:9.2.1 Purify the commercial grade of each glycol needed bycareful fractionation in glass at reduced pressure, discardingthe first

39、 30 % and retaining the next 30 % as the “hearts cuts.”Analyze these fractions as described in Section 10 to be surethey are free of other homologues of the glycol.9.2.2 Prepare a standard mixture of these glycols whosecomposition approximates that of the glycol to be analyzed.The composition of the

40、 standard should be known to thenearest 0.001 %. Correct the composition for any water presentusing the equation in 11.2.4. Determine the water content asdescribed in the applicable section of Test Methods E202.9.2.3 Obtain at least two chromatograms of the standardmixture as described in Section 10

41、 and calculate the averagearea percent for each of the glycols present in accordance with11.2.1. Do not include any areas associated with the pressurepeak in calculating the area percentages. Using the weightpercentages in the standard mixture and the average areapercentages, calculate the factor fo

42、r diethylene glycol asdescribed in 11.1.1.Assume a calibration factor of unity for theethylene glycol in the base ethylene glycol standard mixture.9.3 Calibration Method 2:9.3.1 For routine analyses, high-purity, commercial gradesof each glycol may be used. If the gas chromatographicanalysis as desc

43、ribed in Section 10 indicates that the concen-tration of the ethylene glycol in the diethylene glycol to beadded to the base ethylene glycol in the standard mixture doesnot exceed 0.2 area %, the concentration of the impurity isinsignificant at the concentration levels included in the scope ofthis t

44、est method. The base ethylene glycol should contain lessthan 0.05 area % diethylene glycol.9.3.2 Prepare a standard mixture of the glycols whosecomposition approximates that of the glycol to be analyzed.The composition of the standard mixture should be known tothe nearest 0.001 %. Correct the compos

45、ition for any waterpresent using the equation in 11.2.4. Determine the watercontent as described in the applicable section of Test MethodsE202. If the concentrations of the ethylene glycol in thediethylene glycol added to the base ethylene glycol in thestandard mixture does not exceed 0.2 area %, th

46、e concentrationof the impurity is insignificant at the concentration levelsincluded in the scope of this method. The base ethylene glycolshould contain less than 0.1 area % diethylene glycol.9.3.3 Obtain at least two chromatograms of the standardmixture and of the base ethylene glycol in accordance

47、with10.2 and calculate the average area percent for each of theglycols present in accordance with 11.2.1. Do not include anyareas associated with the pressure peak in calculating the areapercentages. Using the mass percent of diethylene glycol addedto the ethylene glycol and the average area percent

48、ages for theglycols calculate the calibration factor for the diethylene glycolin accordance with 11.1.2. Assume the calibration factor ofunity for the ethylene glycol in the base ethylene glycol and thestandard mixture.10. Procedure10.1 Mount the column in the chromatograph, and adjustthe operating

49、conditions in accordance with the parametersgiven in Table 1 (see Note 5). Allow sufficient time for theinstrument to reach equilibrium as indicated by a stable baseline on the chart at the maximum sensitivity setting to be used.NOTE 5The instrument parameters given in Table 1 were developedfor the indicated instrument. The use of other instruments will probablyrequire some adjustment of column temperature, helium flow rate, etc., toachieve retention times similar to those in Table 2. Adjust the parametersso that symmetrical, sharp peaks with satisfactory re