ASTM F1500-1998(2014) Standard Test Method for Quantitating Non-UV-Absorbing Nonvolatile Extractables from Microwave Susceptors Utilizing Solvents as Food Simulants《利用溶剂作为食品模拟物定性测定.pdf

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1、Designation: F1500 98 (Reapproved 2014)Standard Test Method forQuantitating Non-UV-Absorbing Nonvolatile Extractablesfrom Microwave Susceptors Utilizing Solvents as FoodSimulants1This standard is issued under the fixed designation F1500; the number immediately following the designation indicates the

2、 year oforiginal 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.1. Scope1.1 This test method is applicable to complete microwav

3、esusceptors.1.2 This test method covers a procedure for quantitatingnon-UV-absorbing nonvolatile compounds which are extract-able when the microwave susceptor is tested under simulateduse conditions for a particular food product.1.3 The values stated in SI units are to be regarded asstandard. No oth

4、er units of measurement are included in thisstandard.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 o

5、f regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2E260 Practice for Packed Column Gas ChromatographyE682 Practice for Liquid Chromatography Terms and Rela-tionshipsE685 Practice for Testing Fixed-Wavelength PhotometricDetectors Used in Liquid ChromatographyF874 Test Me

6、thod for Temperature Measurement and Pro-filing for Microwave SusceptorsF1317 Test Method for Calibration of Microwave OvensF1349 Test Method for Nonvolatile Ultraviolet (UV) Ab-sorbing Extractables from Microwave Susceptors3. Terminology3.1 Definitions of Terms Specific to This Standard:3.1.1 micro

7、wave susceptorpackaging materials that, whenplaced in a microwave field, are designed to interact with thefield and provide substantial heat to the package contents.3.1.2 nonvolatile extractablesthose chemical specieswhich released from microwave food packaging under simu-lated use conditions and ar

8、e detected using an applicablenonvolatile extractables method.4. Summary of Test Method4.1 Nonvolatile extractables are determined by subjecting asample of the susceptor material to microwave heating undersimulated use conditions. The sample is washed with solventscovering a range of polarities. The

9、 solvent washes are com-bined and the solvents evaporated just to dryness. The residueis redissolved in a measured quantity of chloroform and thesample split for gravimetric or other analyses, such as HPLC orIR. For the gravimetric determination, a measured portion ofthe sample is filtered and evapo

10、rated and the residue weighed.For other analyses, the remainder of the sample is evaporatedand may be reconstituted in dimethylacetamide prior to injec-tion (see Test Method F1349 for quantitation of UV-absorbingnonvolatiles by HPLC), or treated appropriately prior toexamination by other chromatogra

11、phic or spectroscopic meth-ods.5. Significance and Use5.1 This test method was developed to measure non-UV-absorbing nonvolatile extractables that may be present andmigrate from a microwave susceptor material during use. Itmay be a useful procedure to assist in minimizing the amountof non-UV-absorbi

12、ng nonvolatile extractables either throughsusceptor design or manufacturing processes.5.2 Supplementation of this procedure with other analyticaltechnologies such as high-pressure liquid chromatography,supercritical fluid chromatography, or infrared or other formsof spectroscopy may provide the anal

13、yst with additionalinformation regarding the identification of the components ofthe non-UV-absorbing nonvolatile extractables in the suscep-tor.1This test method is under the jurisdiction of ASTM Committee F02 on FlexibleBarrier Packaging and is the direct responsibility of Subcommittee F02.15 onChe

14、mical/Safety Properties.Current edition approved April 1, 2014. Published April 2014. Originallyapproved in 1994. Last previous edition approved in 2008 as F1500 98(2008).DOI: 10.1520/F1500-98R14.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at

15、 serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States16. Apparatus and Reagents6.1 Microwave Oven, 700 6

16、35 W, no turntable, calibratedin accordance with Test Method F1317.6.2 Extraction Cell, Waldorf, described in Test MethodF1349.NOTE 1If the cell is not equipped with a PTFE gasket, cut a gasketring to match the size of the sleeve from a116 -in. PTFE sheet. Use of thegasket between the sleeve and the

17、 sample reduces damage to the sample.6.3 Microwave Temperature Measurement System.6.4 Temperature Probe, high temperature.6.5 Beaker, 400-mL borosilicate glass.6.6 Hexane, analytical reagent grade or better.6.7 Acetonitrile, analytical reagent grade or better.6.8 Methylene Chloride, analytical reage

18、nt grade or better.6.9 Chloroform, analytical reagent grade or better.6.10 Dimethylacetamide, HPLC grade or better.6.11 Methanol, analytical reagent grade or better, dried overanhydrous sodium sulfate.6.12 Distilled Water.6.13 Nitrogen, grade suitable for solvent evaporation pur-poses.6.14 Rotary Ev

19、aporator, or equivalent.6.15 Weighing Boat, aluminum, formed by shaping alumi-num foil into a round boat approximately 1.5 cm in diameter.6.16 Filter, 0.45 m, compatible with chloroform.6.17 Round-Bottom Flask, 250 mL, with neck to fit rotaryevaporator.6.18 Vial, 20 mL.6.19 Heat Lamp, 125 W, or equi

20、valent.6.20 Boiling Stones.6.21 Watchglass, 8.5 or 9.0-cm diameter.7. Sampling7.1 The sample of microwave susceptor selected for extrac-tion should be representative of the entire susceptor.7.2 The sample should be undamaged, that is, laminationintact, uncreased (unless this is the normal configurat

21、ion) andunaltered.7.3 Carefully cut a circular portion of the susceptor largeenough to fit the Waldorf cell with the top threaded sleeveremoved. Be sure the sample is cut large enough to fill theentire bottom of the cell. Carefully trim away any frayed edgesbefore testing.7.4 Preclean the susceptor

22、to remove dust and fibers byblowing a stream of nitrogen over the surface for a fewseconds, or by gently brushing the surface with a camel hairbrush.8. Procedure8.1 Calibrate the microwave oven in accordance with TestMethod F1317 to ensure that it is 700 6 35 W.8.2 Determine the sample test conditio

23、ns by using themethod for temperature profiling of microwave susceptors inuse in accordance with Test Method F874.8.3 Place the precut susceptor sample into the bottomsection of the Waldorf cell. Carefully place the polytetrafluo-roethylene polymer (PTFE) gasket on top of the susceptor toprevent tea

24、ring when the cell sleeve is threaded in. Thread thetop sleeve of the cell into the bottom section of the cell,trapping the susceptor sample securely between the gasket andthe bottom of the cell.8.4 Carefully insert a temperature probe (6.4) through thesmall temperature probe port opening of the cel

25、l and ensurethat it maintains good contact with the susceptor surface. Inserta second probe onto a different area of the susceptor in thesame way.8.5 Place 50 mL of distilled water and a boiling chip into a400-mL beaker and place the beaker in the center rear of theoven. Place a watchglass over the

26、opening of the Waldorf cell.8.6 Place the Waldorf cell in the center of the microwaveoven, and microwave the sample on high power for the timedetermined during the temperature profiling procedure.8.7 Compare the temperature profiles obtained in 8.6 withthose obtained from the susceptor in contact wi

27、th product. Ifthe two profiles are in reasonable agreement, proceed to 8.8,otherwise repeat 8.3 through 8.6, using more or less water inthe beaker to adjust the profile appropriately.8.8 Without removing the sample, watchglass, or fiber opticprobes from the cell, allow the sample to cool for 5 min.8

28、.9 Remove the temperature probe(s) from the cell. Rinsethe bottom of the watchglass covering the Waldorf cell with 20mL of hexane, pouring the solvent into the cell. Swirl thesolvent in the cell for 10 s, then pour it into a 250-mLroundbottom flask. Repeat using a second 20-mL aliquot ofhexane.8.10

29、Repeat 8.9 using two 20-mL aliquots of methylenechloride.8.11 Repeat 8.9 using two 20-mL aliquots of acetonitrile.8.12 Repeat 8.9 using two 20-mL aliquots of methanol.8.13 Using a rotary evaporator with a water bath tempera-ture of 50C, reduce the volume of the combined solvents inthe round-bottom f

30、lask to approximately 10 mL. Transfer theremaining solvent to a 20-mL vial. Rinse the roundbottom flaskwith two 1 mL portions of acetonitrile and combine with thecontents of the vial.8.14 Apply a gentle stream of nitrogen to the solvent in thevial. Apply gentle heat as necessary to expedite evaporat

31、ion.Evaporate just to dryness, avoiding any heating after all thesolvent is evaporated.8.15 Pipet 10 mL of chloroform into the vial. Swirl withgentle heating to dissolve the residue in the vial.8.16 Dry a clean aluminum weigh boat by placing under aheat lamp for 5 min. Allow to cool and weigh, recor

32、ding thisweight as “tare.” Filter 8 mL of the chloroform solutionF1500 98 (2014)2through the 0.45-m filter into the tared weigh boat and rinsethe filter with a further 1 mL of chloroform.8.17 Place the weigh boat under the heat lamp and evapo-rate the solvent to a constant weight (60.5 mg). Record t

33、hisweight in milligrams as “A.”8.18 Repeat 8.9 to 8.17 using solvents which have not beenexposed to a susceptor. Record the final weight in milligramsafter evaporation as“ B.”8.19 Evaporate the remaining 2 mL of chloroform solutionfrom 8.15 to dryness. At this point the residue may beredissolved in

34、2 mL of dimethylacetamide with gentle heating,filtered through a 0.45-m filter and injected onto an HPLCsystem operated in accordance with Test Method F1349. (SeePractices E260, E682, and E685 for further information regard-ing HPLC set-up and use.) Other sample preparation schemescan be developed f

35、or specific applications involving otherchromatographic or spectroscopic techniques. The analystshould take the steps necessary to ensure that a representativesample of the residue is obtained, and that the analytes have notbeen degraded by the sample preparation scheme chosen.9. Calculation9.1 Calc

36、ulate total nonvolatile extractable as follows:Total nonvolatile extractable mg/in.2! 5 A 2 tare 2 B! 3108.3 38where:A = weight from 8.17,B = weight from 8.18,tare = weight from 8.16,8.3 = square inches of susceptor exposed in Waldorf cell,8 = volume of solvent evaporated, and10 = total volume of sa

37、mple.10. Precision and Bias10.1 Six laboratories participated in a collaborative study ofnonvolatiles recovered from a bilaminate PETE/adhesive/paperboard susceptor construction obtained from a singlesource. Duplicate analyses were performed at heating times of2 and 5 min using water loads specific

38、to the individualmicrowave ovens. Participants were asked to evaluate threeextraction procedures: Test Method F1349 using Miglyol 812in place of corn oil; Test Method F1349 on extracts from adough similar to a pizza crust consisting of 10:40:50 (w/w/w)Miglyol 812 + water + low-protein flour; and thi

39、s procedure.Each laboratory was supplied with bilaminate susceptors,Miglyol 812 and flour from single lots, and appropriatestandard materials for HPLC quantitation. Table 1 lists thestatistical results for the determination of diethyleneglycoldibenzoate (DEGDB) and polyethylene terephthalate trimer(

40、PETE) migrating from the susceptors, normalized to correctfor the various sample areas used by individual collaborators.NOTE 2UV quantitation was used to establish the test methodsvalidity because of the lack of other widely available detection methods.Precision for non-UV-absorbing compounds is exp

41、ected to be similar forthis procedure.10.2 Since no absolute method is available for comparison,no statement regarding bias can be made for this test method.11. Keywords11.1 extractables, nonvolatile; extractables, non-UV absorb-ing; extraction cell, Waldorf; food simulant, corn oil; foodsimulant, d

42、ough; food simulant, Myglyol; food simulant,solvents; HPLC; microwave; microwave susceptors; Myglyol;nonvolatiles; susceptor; susceptors, microwave; temperaturemeasurement, microwaveASTM International takes no position respecting the validity of any patent rights asserted in connection with any item

43、 mentionedin this standard. Users of this standard are expressly advised that determination of 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 commi

44、ttee and must be reviewed every five years andif not revised, either reapproved or withdrawn. Your comments are invited either for revision of this standard or for additional standardsand should be addressed to ASTM International Headquarters. Your comments will receive careful consideration at a me

45、eting of theresponsible technical committee, which you may attend. If you feel that your comments have not received a fair hearing you shouldmake your views known to the ASTM Committee on Standards, at the address shown below.This standard is copyrighted by ASTM International, 100 Barr Harbor Drive,

46、 PO Box C700, West Conshohocken, PA 19428-2959,United States. Individual reprints (single or multiple copies) of this standard may be obtained by contacting ASTM at the aboveaddress or at 610-832-9585 (phone), 610-832-9555 (fax), or serviceastm.org (e-mail); or through the ASTM website(www.astm.org)

47、. Permission rights to photocopy the standard may also be secured from the ASTM website (www.astm.org/COPYRIGHT/).TABLE 1 Statistical Results for Determination of DEGDBand PETE Migrating From SusceptorsAnalyte/MatrixAmount Extracted, g/in.2Average SlabSrSrCoV,%SRSRCoV,%DEGDB, 2 minDough 13.88 3.82 2

48、.93 21 4.81 35Miglyol 812 42.20 12.79 22.46 53 25.85 61Test MethodF150043.25 4.57 14.09 32 14.81 34DEGDB, 5 minDough 24.15 7.27 8.17 34 10.93 45Miglyol 812 86.26 21.82 24.54 28 32.84 38Test MethodF150085.10 8.70 32.08 38 33.24 39PETE, 2 minDough 1.70 0.56 1.38 81 1.49 87Miglyol 812 54.33 7.46 16.06 30 17.71 33Test MethodF15008.29 1.35 3.14 38 3.42 41PETE, 5 minDough 3.31 1.82 2.04 62 2.73 82Miglyol 812 88.56 2.93 13.90 16 14.20 16Test MethodF150015.65 1.89 6.10 39 6.39 41Gravimetric2min5min254729711869059435811146224585F1500 98 (2014)3