ASTM D6866-2006a Standard Test Methods for Determining the Biobased Content of Natural Range Materials Using Radiocarbon and Isotope Ratio Mass Spectrometry Analysis《使用放射性碳和同位素比率质谱.pdf

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1、Designation: D 6866 06aStandard Test Methods forDetermining the Biobased Content of Natural RangeMaterials Using Radiocarbon and Isotope Ratio MassSpectrometry Analysis1This standard is issued under the fixed designation D 6866; the number immediately following the designation indicates the year ofo

2、riginal adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon (e) indicates an editorial change since the last revision or reapproval.1. Scope*1.1 These test methods do not address environmental im-pact, p

3、roduct performance and functionality, determination ofgeographical origin, or assignment of required amounts ofbiobased carbon necessary for compliance with federal laws.1.2 These test methods are applicable to any product con-taining carbon-based components that can be combusted in thepresence of o

4、xygen to produce carbon dioxide (CO2) gas.1.3 These test methods make no attempt to teach the basicprinciples of the instrumentation used although minimumrequirements for instrument selection are referenced in theReferences section. However, the preparation of samples forthe above test methods is de

5、scribed. No details of instrumentoperation are included here. These are best obtained from themanufacturer of the specific instrument in use.1.4 Currently, there are no ISO test methods that areequivalent to the test methods outlined in this standard.1.5 This standard does not purport to address all

6、 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 of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2D 883 Terminology Rel

7、ating to Plastics3. Terminology3.1 The definitions of terms used in these test methods arereferenced in order that the practitioner may require furtherinformation regarding the practice of the art of isotope analysisand to facilitate performance of these test methods.3.2 Terminology D 883 should be

8、referenced for terminol-ogy relating to plastics. Although an attempt to list terms in alogical manner (alphabetically) will be made as some termsrequire definition of other terms to make sense.3.3 Definitions:3.3.1 dpmdisintegrations per minute. This is the quantityof radioactivity. The measure dpm

9、 is derived from cpm orcounts per minute (dpm = cpm bkgd / counting efficiency).There are 2.2 by 106dpm / uCi (14,17).33.3.2 dpsdisintegrations per second (rather than minute asabove) (14,17).3.3.3 scintillationthe sum of all photons produced by aradioactive decay event. Counters used to measure thi

10、s asdescribed in these test methods are Liquid ScintillationCounters (LSC) (14,17).3.3.4 specific activity (SA)refers to the quantity of radio-activity per mass unit of product, that is, dpm per gram (14,17).3.3.5 automated effciency control (AEC)a method usedby scintillation counters to compensate

11、for the effect ofquenching on the sample spectrum (14).3.3.6 AMS facilitya facility performing Accelerator MassSpectrometry.3.3.7 accelerator mass spectrometry (AMS)an ultra-sensitive technique that can be used for measuring naturallyoccurring radio nuclides, in which sample atoms are ionized,accele

12、rated to high energies, separated on basis of momentum,charge, and mass, and individually counted in Faraday collec-tors. This high energy separation is extremely effective infiltering out isobaric interferences, such thatAMS may be usedto measure accurately the14C/12C abundance to a level of 1 in10

13、15. At these levels, uncertainties are based on countingstatistics through the Poisson distribution (8,9).3.3.8 background radiationthe radiation in the naturalenvironment; including cosmic radiation and radionuclides1These test methods are under the jurisdiction of ASTM Committee D20 onPlastics and

14、 are the direct responsibility of Subcommittee D20.96 on Environmen-tally Degradable Plastics and Biobased Products.Current edition approved Oct. 15, 2006. Published October 2006. Originallyapproved in 2004. Last previous edition approved in 2006 as D 6866 - 06.2For referenced ASTM standards, visit

15、the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.3The boldface numbers in parentheses refer to the list of references at the end ofthis standard.1*A

16、 Summary of Changes section appears at the end of this standard.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.present in the local environment, for example, materials ofconstruction, metals, glass, concrete (2,4,7,8,14-19).3.3.9 bio

17、based contentthe amount of biobased carbon inthe material or product as a percent of the weight (mass) of thetotal organic carbon in the product (1).3.3.10 coincidence circuita portion of the electronicanalysis system of a Liquid Scintillation Counter which acts toreject pulses which are not receive

18、d from the two Photomul-tiplier Tubes (that count the photons) within a given period oftime and are necessary to rule out background interference andrequired for any LSC used in these test methods (7,14,17).3.3.11 coincidence thresholdthe minimum decay energyrequired for a Liquid Scintillation Count

19、er to detect a radioac-tive event. The ability to set that threshold is a requirement ofany LSC used in these test methods (14,17).3.3.12 contemporary carbona direct indication of therelative contributions of fossil carbon and “living” biosphericcarbon can be expressed as the fraction (or percentage

20、) ofcontemporary carbon, symbol fC. This is derived from fMthrough the use of the observed input function foratmospheric14C over recent decades, representing the com-bined effects of fossil dilution of14C (minor) and nucleartesting enhancement (major). The relation between fCand fMisnecessarily a fu

21、nction of time. By 1985, when the particulatesampling discussed in the cited reference the fMratio haddecreased to ca. 1.2 (8,9).3.3.13 chemical quenchinga reduction in the scintillationintensity (a significant interference with these test methods)seen by the Photomultiplier Tubes (PMT, pmt) due to

22、thematerials present in the scintillation solution that interfere withthe processes leading to the production of light. The result isfewer photons counted and a lower efficiency (4,7,17).3.3.14 chi-square testa statistical tool used in radioactivecounting in order to compare the observed variations

23、in repeatcounts of a radioactive sample with the variation predicted bystatistical theory. This determines whether two different distri-butions of photon measurements originate from the samephotonic events. LSC instruments used in this measurementshould include this capability (14,17,27).3.3.15 cock

24、tailthe solution in which samples are placedfor measurement in a LSC. Solvents and Scintillators (chemi-cals that absorbs decay energy transferred from the solvent andemits light (photons) proportional in intensity to the depositedenergy) (4,7,14,17).3.3.16 decay (radioactive)the spontaneous transfo

25、rma-tion of one nuclide into a different nuclide or into a differentenergy state of the same nuclide. The process results in adecrease, with time, of the number of original radioactiveatoms in a sample, according to the half-life of the radionuclide(8,14,17).3.3.17 discriminatoran electronic circuit

26、 which distin-guishes signal pulses according to their pulse height or energy;used to exclude extraneous radiation, background radiation,and extraneous noise from the desired signal (14,17,18,32).3.3.18 effciencythe ratio of measured observations orcounts compared to the number of decay events which

27、 oc-curred during the measurement time; expressed as a percentage(14,17).3.3.19 external standarda radioactive source placed adja-cent to the liquid sample in to produce scintillations in thesample for the purpose of monitoring the samples level ofquenching. Required with Method (A) (14,17).3.3.20 f

28、igure of merita term applied to a numerical valueused to characterize the performance of a system. In liquidscintillation counting, specific formulas have been derived forquantitatively comparing certain aspects of instrument andcocktail performance and the term is frequently used tocompare efficien

29、cy and background measures (14,17,20).3.3.21 fluorescencethe emission of light resulting fromthe absorption of incident radiation and persisting only as longas the stimulation radiation is continued (14,17,25).3.3.22 fossil carboncarbon that contains essentially noradiocarbon because its age is very

30、 much greater than the 5730year half-life of14C (8,9).3.3.23 half-lifethe time in which one half the atoms of aparticular radioactive substance disintegrate to another nuclearform. The half-life of14C is 5730 years (8,14,25).3.3.24 intensitythe amount of energy, the number ofphotons, or the numbers

31、of particles of any radiation incidentupon a unit area per unit time (14,17).3.3.25 internal standarda known amount of radioactivitywhich is added to a sample in order to determine the countingefficiency of that sample. The radionuclide used must be thesame as that in the sample to be measured, the

32、cocktail shouldbe the same as the sample, and the Internal Standard must beof certified activity (14,17).3.3.26 modern carbonexplicitly, 0.95 times the specificactivity of SRM 4990b (the original oxalic acid radiocarbonstandard), normalized to d13C = 19 % (Currie, et al., 1989).Functionally, the fra

33、ction of modern carbon equals 0.95 timesthe concentration of14C contemporaneous with 1950 wood(that is, pre-atmospheric nuclear testing). To correct for thepost 1950 bomb14C injection into the atmosphere (9), thefraction of modern carbon is multiplied by 0.93 (as of the year2004).3.3.27 noise pulsea

34、 spurious signal arising from theelectronics and electrical supply of the instrument(14,17,21,29).3.3.28 phase contactthe degree of contact between twophases of heterogeneous samples. In liquid scintillation count-ing, better phase contact usually means higher counting effi-ciency (14,17).3.3.29 pho

35、tomultiplier tube (PMT, pmt)the device in theLSC that counts the photons of light simultaneously at twoseparate detectors (29,32).3.3.30 pulsethe electrical signal resulting when photonsare detected by the Photomultiplier tubes (14,17,18,32).3.3.31 pulse height analyzer (PHA)an electronic circuitwhi

36、ch sorts and records pulses according to height or voltage(14,17,18,32).3.3.32 pulse indexthe number of afterpulses following adetected coincidence pulse (used in three dimensional or pulseheight discrimination) to compensate for the background of aliquid scintillation counter performing (14,18,29,3

37、2).D 6866 06a23.3.33 quenchingany material that interferes with theaccurate conversion of decay energy to photons captured by thePMT of the LSC (2,4,7,14,15,17,20).3.3.34 regionregions of interest, also called windowand/or channel in regard to liquid scintillation counters. Refersto an energy level

38、or subset specific to a particular isotope(4,14,18,21,29).3.3.35 scintillation reagentchemicals that absorbs decayenergy transferred from the solvent and emits light (photons)proportional in intensity to the decay energy (4,14,29).3.3.36 solventin scintillation reagent, chemical(s) whichact as both

39、a vehicle for dissolving the sample and scintillatorand the location of the initial kinetic energy transfer from thedecay products to the scintillator; that is, into excitation energythat can be converted by the scintillator into photons(4.14,17,29).3.3.37 standard count conditions (STDCT)LSC condi-

40、tions under which reference standards and samples arecounted.3.3.38 three dimensional spectrum analysisthe analysis ofthe pulse energy distribution in function of energy, counts perenergy, and pulse index. It allows for auto-optimization of aliquid scintillation analyzer allowing maximum performance

41、.Although different Manufacturers of LSC instruments callThree Dimensional Analysis by different names, the actualfunction is a necessary part of these test methods (14,17,18).3.3.39 true beta eventan actual count which representsatomic decay rather than spurious interference (10,11).3.3.40 flexible

42、 tube crackerthe apparatus in which thesample tube (Break Seal Tube) is placed (5,6,10,11).3.3.41 break seal tubethe sample tube within which thesample, copper oxide, and silver wire is placed.4. Significance and Use4.1 Presidential (Executive) Orders 13101, 13123, 13134,Public Laws (106-224), AG AC

43、T 2003 and other LegislativeActions all require Federal Agencies to develop procedures toidentify, encourage and produce products derived from bio-based, renewable, sustainable and low environmental impactresources so as to promote the Market Development Infrastruc-ture necessary to induce greater u

44、se of such resources incommercial, non food, products. Section 1501 of the EnergyPolicyAct of 2005 (Public Law 10958) and EPA40 CFR Part80 (Regulation of Fuels and Fuel Additives: Renewable FuelStandard Requirements for 2006) require petroleum distribu-tors to add renewable ethanol to domestically s

45、old gasoline topromote the nations growing renewable economy, with re-quirements to identify and trace origin.4.2 Method A utilizes Liquid Scintillation Counting (LSC)radiocarbon (14C) techniques to quantify the biobased contentof a given product with maximum total error of 15 % count,which is assoc

46、iated with sample preparation and actual count-ing. This test method is based on LSC analysis of CO2cocktails after collecting the CO2in a suitable absorbingsolution.4.3 Method B utilizes Accelerator Mass Spectrometry(AMS) and Isotope Ratio Mass Spectrometry (IRMS) tech-niques to quantify the biobas

47、ed content of a given product withpossible uncertainties of 1 to 2 % and 0.1 to 0.5 %, respec-tively. Sample preparation methods are identical to Method A,8.28.5. Method B diverges after 8.5 and rather than LSCanalysis the sample CO2remains within the vacuum manifoldand is distilled, quantified in a

48、 calibrated volume, transferred toa quartz tube, torch sealed. Details are given in 12.7-12.10. Thestored CO2is then delivered to an AMS facility for finalprocessing and analysis.4.4 Method C uses LSC techniques to quantify the biobasedcontent of a product. However, whereas Method A uses LSCanalysis

49、 of CO2cocktails, Method C uses LSC analysis ofsample carbon that has been converted to benzene. This testmethod determines the biobased content of a sample with amaximum total error of 63 % (absolute).4.5 Although MethodsAand C are less sensitive than that ofusing AMS/IRMS, they have two distinct advantages: (1)lower costs per evaluation, and (2) much higher instrumentavailability worldwide. Benzene synthesis is the preferredmethod to be used when sample size is not an issue. Indeed,LSC is the most widely used measurement for14C determ

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