1、Designation: F1884 04 (Reapproved 2018)Standard Test Methods forDetermining Residual Solvents in Packaging Materials1This standard is issued under the fixed designation F1884; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the yea
2、r 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 covers determination of the amount ofresidual solvents released from within a packaging material
3、contained in a sealed vial under a given set of time andtemperature conditions and is a recommended alternative forTest Method F151.1.2 This test method covers a procedure for quantitatingvolatile compounds whose identity has been established andwhich are retained in packaging materials.1.3 The anal
4、yst should determine the sensitivity and repro-ducibility of the method by carrying out appropriate studies onthe solvents of interest. The analyst is referred to Practice E260for guidance.1.4 For purposes of verifying the identity of or identifyingunknown volatile compounds the analyst is encourage
5、d toincorporate techniques such as gas chromatography/massspectroscopy, gas chromatography/infrared spectroscopy orother suitable techniques in conjunction with this test method.1.5 Sensitivity of this test method in the determination ofthe concentration of a given retained solvent must be deter-min
6、ed on a case by case basis due to the variation in thesubstrate/solvent interaction between different types ofsamples.1.6 This test method does not address the determination oftotal retained solvents in a packaging material. Techniquessuch as multiple headspace extraction can be employed to thisend.
7、 The analyst is referred to the manual supplied with theGC-Autosampling system for guidance.1.7 The values stated in SI units are to be regarded as thestandard.1.8 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibility of the use
8、r of this standard to establish appro-priate safety, health, and environmental practices and deter-mine the applicability of regulatory limitations prior to use.1.9 This international standard was developed in accor-dance with internationally recognized principles on standard-ization established in
9、the Decision on Principles for theDevelopment of International Standards, Guides and Recom-mendations issued by the World Trade Organization TechnicalBarriers to Trade (TBT) Committee.2. Referenced Documents2.1 ASTM Standards:2E177 Practice for Use of the Terms Precision and Bias inASTM Test Methods
10、E260 Practice for Packed Column Gas ChromatographyE691 Practice for Conducting an Interlaboratory Study toDetermine the Precision of a Test MethodF151 Test Method for Residual Solvents in Flexible BarrierMaterials (Withdrawn 2004)33. Terminology3.1 Definitions:3.1.1 ream3000 ft2= 278.7 m2= 27.87106c
11、m2.3.1.2 retained solventsthose chemical species, which areretained by packaging material and can be detected in theheadspace of sealed sample vials under conditions of elevatedtemperature.4. Summary of Test Method4.1 Retained volatile organic solvents are determined bysubjecting the packaging mater
12、ial to elevated temperatures in aheadspace sampling system with subsequent gas chromatogra-phy of the headspace and detection using a suitable detectiondevice such as a flame ionization detector (FID).4.2 Volatile components can then be quantified by compari-son with standards of known concentration
13、.4.3 Qualitative analysis may be carried out on a gas chro-matograph (GC) coupled to an appropriate detector capable of1This test method is under the jurisdiction ofASTM Committee F02 on PrimaryBarrier Packaging and is the direct responsibility of Subcommittee F02.15 onChemical/Safety Properties.Cur
14、rent edition approved March 1, 2018. Published April 2018. Originallyapproved in 1998. Last previous edition approved in 2011 as F1884 04(2011).DOI: 10.1520/F1884-04R18.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annua
15、l Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.3The last approved version of this historical standard is referenced onwww.astm.org.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United S
16、tatesThis international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for theDevelopment of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to
17、Trade (TBT) Committee.1compound detection / identification, such as a mass spectrom-eter or infrared detector.5. Significance and Use5.1 This test method is intended to measure volatile organiccompounds that are emitted from packaging materials underhigh-temperature conditions.5.2 This test method m
18、ay be useful in assisting in thedevelopment and manufacture of packaging materials havingminimal retained packaging ink/adhesive solvents.5.3 Modification of this procedure by utilizing appropriatequalitative GC detection devices such as a mass spectrometerin place of the flame ionization detector m
19、ay provide identifi-cation of volatile organics of unknown identity.6. Interferences6.1 Gas ChromatographyBecause of the potentially largenumber of chemical species that can be analyzed using thismethodology, not all species will be resolved from one anotheron a particular GC column under a given se
20、t of conditions.Techniques available to the analyst to verify the identity ofchemical species being quantitated include retention timecomparisons using alternate GC conditions or using an alter-nate GC column. Good judgment in the interpretation ofchromatographic results is always important. Refer t
21、o PracticeE260 for guidance.6.2 ApparatusBecause this method is designed for detect-ing trace quantities of organic compounds, contaminants canlead to misinterpretation of results. Preparing apparatus prop-erly and carrying out blank determinations is essential tominimize this possibility.TEST METHO
22、D A7. Apparatus and Reagents7.1 Gas chromatograph equipped as follows:7.1.1 FID Detector, compatible with capillary columns.7.1.2 Injector, split/split-less compatible with capillary col-umns.7.1.3 Column, DB-5, 30m, 0.25 mm ID, 1 m filmthickness, Cat. No. 1225033, or 0.32 mm, Cat. No.1235033.4A sho
23、rt piece of deactivated fused silica columnmay be placed between the injector and the column to serve asa guard column.7.1.4 Peak Area Integration System, compatible with GCsystem in use. Alternately, a chart recorder and hand integra-tion can be used.7.1.5 Auto sampler is recommended.7.2 Standard S
24、olutions, consisting of the organic solventmixture of interest, at concentrations that simulate the expectedretention levels. 4-Heptanone may be added to the solutions foruse as an internal standard as described in Practice E260.7.2.1 An example of a working standard is listed below. Thestandard use
25、d will vary based on the solvents present in thesample to be tested. The quantities shown in the table willresult in roughly equivalent size peaks due to differences indetector response. If the solvents are mixed neat, adding 1 Lper gram of material in the headspace vial provides a goodstarting poin
26、t for calibration.7.2.2 If desired, water may be used as the diluent for thestandard. The solvents are diluted in 1 L of water, typically 2mL of the resulting solution is added per gram of sample in theheadspace vial for calibration. 2 mL of 20 l/L of 4-heptanonecontaining solution in water can be u
27、sed as an internalstandard.NOTE 1Water will change the partition coefficient between the sampleand retained solvents.Solvent L/L g/mLMethanol 120 94.96Ethanol 80 63.142-Propanol 60 47.13n-Propanol 60 48.21Methylethyl ketone 40 32.20Ethylacetate 40 36.082-Propylacetate 20 17.08Benzene 10 8.76Methylis
28、obutylketone 20 16.02Toluene 10 8.70Heptanone 20 16.427.3 Vials, 20 mL. To ensure against extraneous peaks in thegas chromatographic traces, wash vials thoroughly and dry ina 125C air oven for a minimum of 4 h before using.7.4 Vial Crimp Caps.7.5 Septa, Teflon/Silicone. To ensure that the septa are
29、freeof volatiles, condition the septa in a vacuum oven at 130C for16 h.7.6 Crimping Tool for Vials.4,57.7 Syringe2 mL gas tight with valve.4,6Store syringe in90C oven between uses.7.8 4-Heptanone.4,77.9 For Manual Injection OnlyHot air oven and heatresistant gloves.8. Instrument Setup8.1 Set up the
30、gas chromatographic system per the manu-facturers recommendations and as follows:8.1.1 Injector Temperature250C.8.1.2 Detector Temperature250C.8.1.3 Column Temperature:8.1.3.1 Initial 40C for 4 min.8.1.3.2 ProgramAdjust temperature program to give aretention window of at least 15 min to ensure optim
31、umseparation of solvents.4The sole source of supply of the apparatus known to the committee at this timeis J. and W. Scientific, Cat. No. 122-5033 and Cat. No. 123-5033. If you are awareof alternative suppliers, please provide this information to ASTM Headquarters.Your comments will receive careful
32、consideration at a meeting of the responsibletechnical committee, which you may attend.5The sole source of supply of the apparatus known to the committee at this timeis Cat. No. 33280, Supelco Inc., Bellefonte, PA 16823.6The sole source of supply of the apparatus known to the committee at this timei
33、s Cat. No. 050034, Alltech, 2051 Waukegan Rd., Deerfield, IL 60015.7The sole source of supply of the apparatus known to the committee at this timeis Cat. No. 10, 174-5, Aldrich, 940 W. St. Paul Ave., Milwaukee, WI 53233.F1884 04 (2018)28.1.4 Attenuation or sensitivity, or both, set to give adetector
34、 response of 40 % or more of full scale on the recorderor integrator of the expected internal standard and standardsample response. See Practice E260 for guidance.8.2 Set up autosampler, if used, to heat vials for 20 min at90C before autoinjection.9. Calibration Procedure9.1 Standard Curve:9.1.1 Pre
35、pare blanks by heating a sample of the packagingmaterial of interest (enough sample can be prepared at one timefor several analysis runs) in a vacuum oven at 90C for 24 h.Remove the blanks and store in a closed container. Blanksshould be cut to the same relative size as the sample prior toheating in
36、 the vacuum oven.9.1.2 To prepare a calibration standard place a blank (cut toappropriate size) in the 20 mL headspace vial and add theappropriate amount of standard solvent mix to the vial.Immediately cap and crimp the vial with the Teflon side of theseptum toward the vial. It is suggested that bla
37、nks be fortifiedat five different concentrations along with an unfortified blankbe prepared for calibration. See Practice E260 for guidance.9.2 Manual Injection:9.2.1 If using a syringe and hot air oven, heat each vial for20 min at 90C. Ensure that the syringe is heated to at least90C before taking
38、headspace samples from the vials forinjection into the chromatograph.NOTE 2When handling the hot syringe be sure that hands areadequately protected. Fill the gas tight syringe with 1 mL of air, closevalve and insert the needle through the septum into the preheated vial.Open valve, inject the air int
39、o vial. Draw12 mL of gas from vial intosyringe, inject back into vial. Repeat 2 times. Draw exactly 1 mL of gasinto syringe and close valve. Insert needle into injector of GC and inject.NOTE 3Consistent technique from injection to injection of standardsand sample is required. This step should take n
40、o more than 30 s.9.3 Automated InjectionThe recommended method of in-jecting the headspace gas into the GC is use of an automatedheadspace sampling system where the vials are heated to 90Cfor 20 min and then the headspace of each vial is automaticallyinjected onto the GC column.9.4 Repeat the proced
41、ure for all five calibration standardsand the blank.9.5 Construct a standard calibration curve from the dataobtained using standard techniques as defined in Practice E260.NOTE 4Longer heating times may be used if it is deemed necessary toensure that the solvent in the headspace of the vial has total
42、ly equilibratedwith the sample.10. Sampling10.1 Samples should be taken in such a manner as torepresent the entire web. The analyst should cut several layersdeep into a roll of packaging material, discarding the outerlayers, to ensure the sampling is representative of the entireroll. Samples should
43、be taken from the left, center and rightside of the web.NOTE 5Consideration should also be given when sampling rollswithin a production lot to ensure uniformity within the production run.10.2 Samples should be taken and handled in such a way asto minimize loss of solvent from the sample between the
44、timethe sample is taken, cut and loaded into the sample vial. Takingsamples at press side, cutting and loading into vials immedi-ately is the preferred method.Alternately, full web samples canbe collected at press side and placed in a sealed container(samples can also be wrapped tightly in foil) for
45、 transport to thelab for cutting and loading into vials.10.3 When taking samples from roll stock, discard the first8 to 10 layers before taking samples from the next 30 to 40layers to ensure that the samples are representative of the entireroll.10.4 When possible, samples should have 100 % ink cov-e
46、rage in the area selected for testing. Selecting an area with100 % ink coverage will ensure that the testing will elucidate aworst case. Using a sample area with representative inkcoverage may also be considered.10.5 The sample size is dictated by the thickness of thesample and the ease of filling t
47、he vial. The sample size willvary from 5 to 50 in.2Typically, the vial will be less than 20 %full by volume. Alternately the ratio of the weight of thesample in grams to the volume of the vial in millilitres shouldnot exceed 1 to 10. In the case of a 20-mL sample vial, theweight of the sample should
48、 not exceed 2 g.10.6 The preferred method of cutting samples is the use ofa punch press or die.10.7 Add the appropriate amount of internal standard (ifused) to the vial.10.8 Immediately cap and crimp the vial with the Teflonside of the septa toward the vial.11. Procedure11.1 Manual Injection:11.1.1
49、For those using the syringe, place the sample (vial) ina forced air oven at 90C for 20 min.NOTE 6Longer heating times may be used if it is deemed necessary toensure that the solvent in the headspace of the vial has totally equilibratedwith the sample.NOTE 7When handling the hot syringe be sure that hands areadequately protected. Fill the preheated gas-tight syringe with 1 mLof air,close valve and insert the needle through the septum into the aboveconditioned vial. Open valve, inject the air into vial. Draw12 mL of gasfrom vial into syringe, in
