ASTM C1561-2010 Standard Guide for Determination of Plutonium and Neptunium in Uranium Hexafluoride by Alpha Spectrometry《α光谱法测定铀六氟化物中钚和镎的标准指南》.pdf

1、Designation: C1561 10Standard Guide forDetermination of Plutonium and Neptunium in UraniumHexafluoride and U-Rich Matrix by Alpha Spectrometry1This standard is issued under the fixed designation C1561; 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. Scope1.1 This method covers the determination of plutonium andneptunium isotopes in uranium hexa

3、fluoride by alpha spectros-copy. The method can also be applicable to any matrix that maybe converted to a nitric acid system.1.2 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 ap

4、pro-priate safety and health practices and determine the applica-bility of regulatory requirements prior to use.2. Referenced Documents2.1 ASTM Standards:2C787 Specification for Uranium Hexafluoride for Enrich-mentC996 Specification for Uranium Hexafluoride Enriched toLess Than 5 %235UC1163 Practice

5、 for Mounting Actinides for Alpha Spec-trometry Using Neodymium FluorideC1475 Guide for Determination of Neptunium-237 in SoilD1193 Specification for Reagent WaterD3084 Practice for Alpha-Particle Spectrometry of WaterD3648 Practices for the Measurement of Radioactivity3. Terminology3.1 reagent blan

6、kDI water processed the same as thesamples; used in the determination of the minimum detectableactivity.3.2 region-of-interest (ROI)the channels, or region, in thealpha spectra in which the counts due to a specific radioisotopeappear on a functioning calibrated alpha spectrometry system.4. Summary o

7、f Test Method4.1 An aliquot of hydrolyzed uranium hexafluoride equiva-lent to approximately 0.5 g of uranium is converted to an oxalicacid-nitric acid system and the uranium is selectively removedvia solid phase extraction. Plutonium and neptunium arefurther purified by additional solid phase extrac

8、tions. Theplutonium and neptunium are then co-precipitated with neody-mium as the fluorides and counted by alpha spectrometry.4.2 Tracer recoveries using this method are typically be-tween 75 and 90 % for uranium hexafluoride, for differentmatrix (with impurities): 10 %. The resolution of the tracer

9、 istypically less than 40 keV full-width at half-maximum.4.3 The minimum detectable activity will vary with tracerrecovery, sample size, instrument background, and countingefficiency.5. Significance and Use5.1 The method is applicable to the analysis of materials todemonstrate compliance with the sp

10、ecifications set forth inSpecifications C787 and C996.5.2 The method can be used to quantify Pu and Np in U-richmatrix before to recycle them.6. Interferences6.1 Incomplete removal of U-234 from the neptuniumfraction could result in a false positive for the Np-237 analysis.The method has been shown

11、to adequately remove uranium atenrichments up to 5 %. If the method is used for the analysis ofmaterials at greater than 5 % enrichment, a blank consisting ofuranium at the same enrichment as the samples should beanalyzed to show adequate removal of the U-234.6.2 A Pu tracer is used to monitor the c

12、hemical recovery ofthe Np. Spiked analyses should be performed to confirm theappropriateness of this correction; fractionation of Np and Puduring the separation could lead to incorrect test results.7. Instrumentation7.1 Alpha Spectrometry SystemSee Practices D3084 andD3648 for a description of the a

13、pparatus.1This guide is under the jurisdiction of ASTM Committee C26 on Nuclear FuelCycle and is the direct responsibility of Subcommittee C26.05 on Methods of Test.Current edition approved Oct. 1, 2010. Published October 2010. Originallyapproved in 2003. Last previous edition approved in 2003 as C1

14、561-03. DOI:10.1520/C1561-10.2For referenced ASTM standards, visit 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.1Copyright ASTM International, 1

15、00 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.8. Apparatus8.1 Ion Exchange Columns, able to hold a 10 mL resin bedand 15 mL solution washes.8.2 Filter Paper, 0.1 m pore size, 25-mm diameter, com-patible with HF.39. Reagents and Materials9.1 Purity of ReagentsReag

16、ent grade chemicals shall beused in all tests. Unless otherwise indicated, it is intended thatall reagents shall conform to the specifications of the Commit-tee on Analytical Reagents of the American Chemical Society,where such specifications are available.49.2 Purity of WaterUnless otherwise indica

17、ted, referencesto water shall be understood to mean reagent water as definedin Specification D1193.9.3 Ammonium Oxalate (0.1M)Dissolve 12.4 g ammo-nium oxalate in approximately 500 mL of water and dilute to1L.9.4 Ascorbic Acid Solution (Saturated)Add ascorbic acidto 2M nitric acid while stirring unt

18、il no more ascorbic acid willdissolve. Prepare fresh when needed for use.9.5 Ethanol, ethyl alcohol, absolute (200 proof), denatured.9.6 Hydrochloric Acid (HCl), specific gravity 1.19, concen-trated.9.7 Hydrochloric Acid, 9MAdd 750 mL concentrated HClto 100 mL of water, dilute to a final volume of 1

19、 L.9.8 Hydrochloric Acid, 4MAdd 333 mL of concentratedHCl to 500 mL of water; dilute to a final volume of 1 L.9.9 Hydrochloric Acid, 1.5MAdd 125 mL of concentratedHCl to 500 mL of water; dilute to a final volume of 1 L.9.10 Hydrochloric Acid, 1MAdd 83 mL of concentratedHCl to 500 mL of water; dilute

20、 to a final volume of 1 L.9.11 Hydrofluoric Acid (HF), concentrated HF, minimumassay 48 %.9.12 Iron (III) Nitrate (10 mg Fe/mL)Dissolve 18.0 g ofFe(NO3)39H2O in 250 mL of water.9.13 Neodymium Chloride (10 mg Nd/mL)Add 25 mLconcentrated HCl to 1.17 g neodymium oxide and heat at100C until dissolved. A

21、llow solution to cool and dilute to 100mL with water.9.14 Neodymium Chloride (100 g Nd/mL)Dilute 1 mL ofthe 10 mg Nd/mL solution to 100 mL with water.9.15 Nitric Acid (HNO3), concentrated nitric acid, specificgravity 1.42.9.16 Nitric Acid (3M)Add 188 mL concentrated nitricacid to 500 mL of water; di

22、lute to a final volume of 1 L.9.17 Nitric Acid (2M)Add 125 mL of concentrated nitricacid to 500 mL of water; dilute to a final volume of 1 L.9.18 Oxalic Acid in 1M HCl (0.1M)Dissolve 12.6 g oxalicacid dihydrate in 500 mL of 1M HCl; dilute to a final volumeof 1 L with 1M HCl.9.19 Oxalic Acid in 2M HN

23、O3(0.1M)Dissolve 12.6 goxalic acid dihydrate in 500 mL of 2M HNO3; dilute to a finalvolume of 1 L with 2M HNO3.9.20 Pu-236 or Pu-242 Tracer, traceable to a national orinternational standard.9.21 Sodium Nitrite (100 mg/mL)Dissolve 500 mgNaNO2in 5 mL water. Prepare fresh when using.9.22 Extraction Chr

24、omatography Resin, containingoctylphenyl-N,N-di-isobutyl carbamoylphosphine oxide(CMPO) dissolved in tri-n-butyl phosphate (TBP) as theimmobilized extractant.5,69.23 Extraction Chromatography Resin, containing diamylamylphosphonate (DAAP) as the immobilized extractant.7,810. Calibration and Standard

25、ization10.1 The alpha spectrometry units should be calibrated forenergy, resolution and efficiency according to the manufactur-ers instructions. The background counting rate for the instru-ment should be measured at a frequency determined by theuser. See Practices D3084 and D3648 for additional info

26、rma-tion.11. Procedure11.1 Uranium Removal:11.1.1 Pipette an aliquot of hydrolyzed UF6sample equiva-lent to 0.05 to 0.5 g uranium into a beaker. Add the Pu tracerto the sample and evaporate to dryness. Add 10 mL concen-trated nitric acid and evaporate to dryness. This operation maybe repeated to rem

27、ove fluoride. Option: Neptunium-239 can beadded as an independent tracer for the Np-237; see GuideC1475 for its use.11.1.2 Prepare 2 DAAP extraction columns per sample byadding resin slurried in water to the column.Allow the water todrain to obtain a 10 mL bed volume. Condition the columns byadding

28、15 mL of the oxalic acid in 2M nitric acid solution.Allow the solution to pass through the columns.11.1.3 Dissolve the sample residue in the beaker above byadding 15 mLof the oxalic acid in 2M nitric acid solution. Heatgently to complete the dissolution. Add the sample to the firstof the extraction

29、columns and collect the load solution in aclean beaker.Add an additional 15 mL of the oxalic acid in 2Mnitric acid solution to the column and collect the rinsate in thesame beaker.NOTE 1The column retains the U; Pu and Np will pass through in theload and rinse solutions.11.1.4 Add the combined solut

30、ions from the two stepsabove to the second DAAP extraction column. Collect the load3The Gelman Metricel filter has been found to be acceptable.4Reagent Chemicals, American Chemical Society Specifications, AmericanChemical Society, Washington, DC. For suggestions on the testing of reagents notlisted

31、by the American Chemical Society, see Analar Standards for LaboratoryChemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeiaand National Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.5Horwitz, E. P., Chiarizia, R., Dietz, M. L., Diamond, H., and Nelson, D.,

32、 “Separation and Preconcentration of Actinides from Acidic Media by ExtractionChromatography,” Analytica Chemica Acta, 281, 1993, pp. 361-372.6TRU resin from EIChroM Industries, Darien IL, USA, has been found to beacceptable.7Horwitz, E. P., Dietz, M. L., Chiarizia, R., Diamond, H., Essling, A. M.,

33、andGraczyk, D., “Separation and Preconcentration of Uranium from Acidic Media byExtraction Chromatography,” Analytica Chemica Acta, 266, 1992, pp. 25-37.8U-TEVAresin from EIChroM Industries, Darien IL, USA, has been found to beacceptable.C1561 102solution in a clean beaker. Rinse the column with 15

34、mL of theoxalic acid in 2M nitric acid solution and collect in the samebeaker.11.1.5 Evaporate the combined solution from above todryness. Add 10 mL of concentrated nitric acid to the beakerand evaporate to dryness.NOTE 2Elute the uranium from the DAAP columns by adding 40 mLof 0.1M ammonium oxalate

35、. Dispose of the eluant containing the uraniumaccording to site specific disposal procedures.11.2 Preparation of Plutonium and Neptunium for Count-ing:11.2.1 Dissolve the residue from above in 10 mL of 3Mnitric acid by gently heating. Add 1 mL of the 10 mg Fe/mLsolution and 2.5 mL of the saturated a

36、scorbic acid solution tothe sample.NOTE 3The ascorbic acid reduces the Fe from +3 to +2; the Fethen serves to reduce the Pu from +4 to +3 and the Np from +5 to+4.NOTE 4Hydroxylamine chlorhydrate can be used instead of ascorbicacid.NOTE 5It is possible to work without Fe when only Pu is necessary.11.

37、2.2 Prepare one CMPO-TBP extraction column persample by loading 2 mL of resin per column.9Condition thecolumn by adding 5 mL of 3M nitric acid to the column andallowing it to drain completely through.11.2.3 Add the sample to the column and allow it to passthrough the column. Rinse the column with 5

38、mL of 3M nitricacid. Discard all the rinses.11.2.4 Add 0.1 mL of the 100 mg/mL sodium nitritesolution to 5 mL of 2M nitric acid and swirl to mix. Add thissolution to the column.NOTE 6The sodium nitrite oxidizes the Pu from +3 to +4.11.2.5 Rinse the column with 10 mL of 2M nitric acid.11.2.6 Rinse th

39、e column, in succession, with 5 mL 9M HCl(crossover solvent), 10 mL 4M HCl (elutes Am) and 35 mL1.5M HCl (elutes Th). Discard all the rinses.11.2.7 Place a PTFE beaker under the column. Elute theplutonium and neptunium by adding 15 mL of the oxalic acidin 1M HCl solution.11.3 Preparation for Countin

40、g:NOTE 7Refer to Test Method C1163 for additional guidance.11.3.1 Add 0.5 mL of the 100 g Nd/mL solution and 1 mLof concentrated HF to the Np and Pu fraction from above andmix. Allow the sample to sit for 30 min.11.3.2 Place a 0.1 m, 25-mm diameter filter on a vacuumflask. Rinse the filter first wit

41、h ethanol and then with water.11.3.3 Pour the sample through the filter. After the samplesolution has passed through the filter rinse the filter with waterand then with ethanol, allowing each solution to pass com-pletely prior to the next one. Remove the filter from the flaskand dry under a heat lam

42、p.11.3.4 Count the sample in a calibrated alpha spectrometrysystem for an appropriate amount of time.11.3.5 Confirm the removal of uranium by examining theU-238 region of the alpha spectrum. If detectable uraniumremains the Np-237 must be corrected for the U-234 in thesame region, or the sample shou

43、ld be re-extracted.NOTE 8Alternatively, electrodeposition can be used (refer to elec-trodeposition guide).12. Calculations12.1 Calculation of Tracer Yield:Y 5 Gt2 Bt! / E At! (1)where:Y = chemical yield,Gt= gross counts per second in the Pu tracer ROI,Bt= background counts per second in the Pu trace

44、r ROI,E = detector counting efficiency (cps/dps), andAt= activity of the Pu tracer in Bq (dps).12.2 Calculation of Activity:The following equation is used to calculate the activity in thesample including any possible reagent blank:Ai5 Gi2 Bi! / Gt2 Bt!# At/ ABi W!# (2)where:Ai= activity of isotope o

45、f interest in Bq per gram U(Pu-238, Pu-239+240, Np-237),Gi= gross counts per second in the analyte ROI,Bi= background counts per second in the analyte ROI,ABi= abundance of alpha decay in ROI, expressed as afraction, andW = weight of U analyzed, g.Additional calculations, including reagent blank sub

46、traction,can be found in Practice D3084.12.3 Calculation of Minimum Detectable Activity:MDAi5 4.65 SB1 2.71! / E Y T ABi W! (3)where:MDA = minimum detectable activity (Bq/g),SB= standard deviation of the reagent blank counts, andT = counting time, s.13. Keywords13.1 alpha spectrometry; neptunium; pl

47、utonium; uraniumhexafluoride9The prepacked TRU column available from EIChroM Industries has beenfound to be acceptable.C1561 103APPENDIX(Nonmandatory Information)X1.X1.1 This method does not have sufficient data to bequalified as a Standard Method for ASTM but is offered as aGuide for those wishing

48、options for the analysis of Pu and Npin UF6. At present there are no Certified Reference Materialsavailable from the national standards bodies to provide acomplete Precision and Bias statement, however the informa-tion below is offered as an example of data produced followingthis Guide.X1.2 Twenty s

49、amples of UF6were spiked at the 0.01 Bq/g(0.27 pCi/g) level with Np-237 and with Pu-239 and analyzedto give an indication of the precision and bias. The relativestandard deviation of the 20 results was determined to be 15 %and 14 % for Np-237 and Pu-239, respectively, as an indicationof precision. The percent recovery was 103 % and 98 % forNp-237 and Pu-239, respectively, as an indication of bias.ASTM International takes no position respecting the validity of any patent rights asserted in connection with any i