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New Applications of Rapid Column Extraction for Methods at SRS. Sherrod L. Maxwell III Savannah River Site. Recent Developments/Applications. Current Actinide Methods Pu/Np/U/Am Sequential methods using TEVA/UTEVA/TRU Resin in F Area Process Lab (alpha, TIMS, ICP-MS)
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New Applications of Rapid Column Extraction for Methods at SRS Sherrod L. Maxwell III Savannah River Site
Recent Developments/Applications • Current Actinide Methods • Pu/Np/U/Am Sequential methods using TEVA/UTEVA/TRU Resin in F Area Process Lab (alpha, TIMS, ICP-MS) • Sequential Pu/Am/ Sr using TRU/SR Resin in Bioassay Lab • New Applications • Sequential column extraction in Bioassay Lab to replace anion resin methods for Pu,Np and U plus enhanced Sr method using cartridge technology • UTEVA for Pu/U removal for Pu/U oxides (Impurity assay) • Actinides in soil using Diphonix Resin-microwave digestion
Bioassay Application • Current methods • Pu-acidified 500 mL samples/evaporated -AG-1 anion resin • U-acidified 50 mL samples/evaporated -AG-1 anion resin • Pu/Am/Sr- 500 mL calcium phosphate/ TRU + SR Resin • Need more efficient, consistent, sequential methods; larger aliquots for special samples
Bioassay ApplicationSherrod L. Maxwell, David J. Fauth, Gerald D. Levi • New Methods • Expand use of calcium phosphate precipitation (500 ml to 1000+ mL) • Enhance vacuum column extraction with cartridge work • Pu (Np when Pu-236 tracer used) on TEVA • U on UTEVA • Pu, (Np)/U using TEVA/UTEVA cartridge technology • Pu, (Np)/Sr using TEVA/Sr cartridge technology
Bioassay Application • Advantages • Faster, more consistency, less acid waste; reduced labor costs; facilitates sequential analysis; better alpha peak resolution • Better detection limit for uranium-500 mL+ sample (vs. current 50 mL sample size) • Cartridge technology more efficient; eliminates large sequential load solutions (evaporation steps)
Challenges • Optimize nitrate levels for Pu, Np on TEVA and U, Sr UTEVA/SR Resin work using cartridges • Achieve adequate Th-228 removal for Pu/U work • Interface with current electroplating practices (Phase II, go to cerium fluoride precipitation)
Bioassay Implementation Status • Final testing near completion • Implementation over next 3 to 4 months • Pu-TEVA • Pu, Np -TEVA • Pu, (Np)-Sr -TEVA/SR Resin • Pu, (Np)-U -TEVA/UTEVA
Sample Preparation • Tracer addition (Pu-242 or Pu-236, U-232) • Routine calcium phosphate precipitation • 3 mmol Ca (120 mg )+ 15 mmol (NH4)2HPO4 • Precipitate/centrifuge/redissolve/ash • Redissolve in 6 mL of 6M HNO3 • Add 2.5 M Al(NO3)3 -scrubbed using UTEVA • 7.5 mL for for Pu, Np or Pu, Np/U • 5 mL for Pu, Np/Sr • Valence adjust Pu and Np: 1; ferrous sulfate 1mL 1.5 M FeSO4. 2; sodium nitrite (1mL of 3M NaNO2)
Sample Preparation (contd.) • Add 16M HNO3 as appropriate to increase acidity of load solution • 1 mL for Pu, Np/U(adjust acidity to 2.5 to 3.5M) • 2 mL for Pu, Np/Sr (adjust acidity to 4.5-5M)
Pu-Recoveries Using TEVA/UTEVA Resin 500 mL urine sample/ Pu-242 tracer= 1.25 dpm %Recovery (microprecipitation) % Recovery (Electroplating* ) 1) 110 1) 84.4 2) 93.3 2) 72.4 3) 92.6 3) 69.3 4) 95.2 4) 69.6 5) 101.5 5) 79.8 6) 99.3 6) 84.5 7) 97.7 7) 79.1 8) 115.4 8) 85.5 9) 107.9 9) 84.8 10) 106.8 Avg. = 102% Avg. = 79% *Add 4 mL 0.02M H2SO4 to enhance F removal during solution cleanup
U Recoveries Using TEVA/UTEVA Cartridge 500 mL urine sample / U-232 tracer= 0.582 dpm % Recovery (Electroplating*) 1) 77.1 2) 84.5 3) 95.5 4) 75.9 5) 73.5 6) 71.1 7) 65.0 8) 74.7 9) 88.0 10) 106.2 Avg. = 81% * Used 0.02MHCl-0.02MHF instead of 0.02M H2SO4 for electroplating
Sr Recoveries using TEVA/Sr Cartridge • 500 mL urine sample Sr-90 spiked in samples: 206 dpm Measured dpm % Recovery 180 87.4 179 87.9 189 91.7 179 86.9 19795.6 Avg 185 89.7 Sr-90 Spiked after precipitation: Measured: % Recovery 215 104% 216 105%
Pu/U Removal for Impurity AssaySherrod L. Maxwell, Sheldon. T. Nichols, Vernon Jones, Maureen Schilb Background • AG MP-1 Anion Resin for Pu Removal prior to ICP-AES of impurities in metal/oxides to removal spectral interference: • Problem: at least partial retention of Au, Ag, Pt, Ir, Pd, Nb, Tl, La, Ce and Ta on resin • Increased need to analyze mixed Pu/U materials requiring Pu/U removal • UTEVA Resin offers improved impurity recovery and removes Pu and U
UTEVA Removal of Pu and U • UTEVA Resin (diamylamylphosphonate) • Recovers all impurities except Au* • Zr, Ta, Hf, Nb require dilute HF in column load solution • Handles Pu, U or Pu/U mixtures • Large 10 mL columns remove 200 mg or more of Pu/U * Au done by dilute HCL-HF cation method
UTEVA Pu/U Removal Method • Load solution: 10 mL 8 M HNO3-0.04M HF • Column Rinse: 14 mL 8M HNO3 (optional with HF) (no HF in rinse to enhance Pu retention; still adequate recovery of Zr, Ta, Hf, Nb; may increase HF with U only to increase Ta, etc., balancing Si background at ICP-torch due to HF) • Adjust to 25 mL in graduated tube • Pu/U recovery from resin: 20 mL 0.1M HCl-0.05M HF • Status: In Use
Analysis of CRM-124 Uranium Oxide Standards Element Measured Ref. Prepared Value/ %Difference (ppm) dc arc range (ppm) Al 102 105 (81-120) -3% Be 11.6 12.5 (10-17) -7% Cr 55.4 52 (50-64) +6% Mg 52.4 51 (37-86) +3% Mo 53.7 50 (30-50) +7% Na 230 200 (189-252) +15% Ni 106 102 (92-158) +4% V 24.2 25 (23-30) -3% W 105 100 (86-95) +5% Zn 110 102 (75-115) +8% Zr 108 100 (67-100) +8% measured = single solution analyzed once by ICP-AES and ICP-MS
Actinide Recovery Method for Large Soil SamplesSherrod L. Maxwell and Sheldon. T. Nichols • Eliminate sample matrix using Diphonix Resin (load in HCL-HF) • Microwave Diphonix Resin to release actinides • Apply sequential actinide analysis using TEVA/UTEVA+ TRU Resins, followed by Am-REE on TEVA Resin • Successfully applied to 10 gram soil fusions/leaches
Summary • New implementation of rapid column methods in bioassay lab will result in significant time/cost savings • New use for UTEVA resin improves impurity analysis for Pu/U oxides/metals • Diphonix resin eliminates matrix problems with large soil samples