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New Extraction Methods for Actinides in Urine at SRS Sherrod L. Maxwell III and David Fauth Savannah River Site.

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Presentation on theme: "New Extraction Methods for Actinides in Urine at SRS Sherrod L. Maxwell III and David Fauth Savannah River Site."— Presentation transcript:

1 New Extraction Methods for Actinides in Urine at SRS Sherrod L. Maxwell III and David Fauth Savannah River Site

2 Recent Applications New Column Extraction Applications at SRS –UTEVA method for Pu/U removal for Pu/U oxides (Impurity assay) –New UTEVA method for Pu and U-Isotope Dilution Mass spectrometry in mixed oxides (strip Pu separately using 3M HNO3-0.2MHF) –Actinides in soil using Diphonix Resin-microwave digestion –Sequential column extraction in Bioassay Lab for Pu, Np, Am, U plus enhanced Sr method using cartridge technology –Pu, Am in fecal samples using Diphonix Resin-microwave digestion and TEVA+TRU Resin

3 Actinides in Urine Current Urine Methods –Pu-acidified 500 mL samples/evaporated -anion resin –U-acidified 50 mL samples/evaporated -anion resin –Pu/Am/Sr- 500 mL calcium phosphate/ TRU + SR Resin Need more efficient, consistent, sequential methods with better Th-228 removal; larger aliquots for special urine samples

4 Bioassay Urine Methods New Methods –Expand use of calcium phosphate precipitation (500 ml to 1000+ mL) –Improve Th-228 removal –Enhance vacuum column extraction with cartridge work –Pu (Np when Pu-236 tracer used) on TEVA Resin –Pu, Np, U, Am using TEVA/TRU column or cartridge technology –Pu, Np, U, Am, Sr using TEVA/TRU +SR columns or cartridge technology

5 Bioassay Application Advantages –Faster, more consistency, less acid waste (0.9 L vs. 6 L per batch); reduced labor costs; 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)

6 Bioassay Implementation Status Implementation over next 3 to 6 months Pu, Np-TEVA -implemented-10/99 Pu, Np, Sr -TEVA /SR cartridge or column Pu, Np, Am -TEVA+TRU cartridge or column Pu, Np, Sr, U,Am -TEVA+TRU cart. + SR column (add 2nd small TEVA column to ensure complete Th-228 removal)

7 Challenges Optimize nitrate levels for Pu, Np on TEVA and Sr on SR Resin work using cartridges Achieve adequate Th-228 removal for Pu/U work –successful with second 1 ml TEVA column Interface with current electroplating practices/evaluate cerium fluoride ppt Improved Pu stripping from TEVA Resin (NH 4 I or Ti +3) Ensure adequate Pu, Np reduction w/o Fe +2 to enable TRU cartridge below TEVA for urine samples

8 Sample Preparation Tracer addition (Pu-242 or Pu-236, U-232, Am-243) Routine calcium phosphate precipitation –3 mmol Ca (120 mg )+ 15 mmol (NH 4 ) 2 HPO 4 Precipitate/centrifuge/redissolve/ash TEVA+TRU: Pu, Np, Am, U, Sr –Redissolve in 6 mL of 5M to 6M HNO 3 –Add 6 mL of 2 to 2.5 M Al(NO 3 ) 3 -scrubbed using UTEVA –after valance adj., no additional acidity adjustment needed TEVA+SR: Pu, Np, Sr –Redissolve in 5 mL of 5M HNO 3 –Add 5 mL of 2 to 2.5 M Al(NO 3 ) 3 -scrubbed using UTEVA –after valance adj., add 3 mL 16M HNO 3 (adjust acidity to 4.5M )

9 Sample Preparation (contd.) Valence options to adjust Pu and Np for TEVA: A.1) Add 1 mL 1.5M ferrous sulfate + 1 mL 1.5M ascorbic acid, wait 3 min. 2) Add 1 mL 3.5M to 4M sodium nitrite For TRU cartridge below TEVA (no iron added) : B. 1) Add 0.5 mL 1.5M sulfamic acid, 2mL 1.5M ascorbic acid, wait 3 to 5 min. 2) 2 mL 4 M sodium nitrite, ensuring excess nitrite

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11 Pu, Np on TEVA RESIN (URINE)

12 TEVA Pu Tracer Recoveries 500 mL urine sample/ Pu-242 tracer= 1.25 dpm / One TEVA Column Fe+AA/+NO 2 %Recovery (CeF 3 microprecipitation) % Recovery (Electroplating* ) 1)1101) 84.4 2) 93.32) 72.4 3)92.63) 69.3 4) 95.24)69.6 5) 101.55) 79.8 6) 99.36) 84.5 7) 97.7 7) 79.1 8) 115.48) 85.5 9) 107.99) 84.8 10)106.810)77.0 11)101.611) 82.5 12)102.6 Avg. =102.0% Avg. = 79.0 *Add 4 mL 0.02M H2SO4 to enhance F removal during solution cleanup for plating

13 TEVA- Np Spike Recoveries 500 mL urine sample/ Np-237 spike= 1.40 dpm Single TEVA column Valence adj. : Fe+AA/+`NO2 % Np-237 Recovery (electroplating) 1)101.6 2) 99.5 3)71.3 4) 104.5 5) 85.8 6) 78.3 7) 85.9 8) 81.3 9) 77.8 10)75.3 11)91.9 12) 105.3 Avg. =88.2%

14 Pu, Np/Am, U, Sr on TEVA/TRU RESIN (URINE)

15 Pu on TEVA RESIN (URINE or FECAL) (2nd Column to Remove all Th-228)

16 TEVA (w/ 2nd Col.) -Pu Tracer Recoveries 500 mL urine sample/ Pu-242 tracer= 1.25 dpm With 2nd 1 mL TEVA Column to ensure complete Th-228 removal when U- 232 added 1+2: Fe+AA/+NO 2 3-7: SA+AA/NO2 %Recovery (CeF 3 microprecipitation) % Recovery (Electroplating* ) 1)93.21) 66.0 2) 90.02) 75.4 3)84.13) 72.7 4) 90.04)71.0 5)86.0 Avg. =89.3% 6)80.9 7)73.0 Avg. = 75.0%

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19 TRU Resin -Am Tracer Recoveries 500 mL urine sample/ Am-243 tracer= 1.55 dpm / TRU cartridge after TEVA SA+AA/+NO 2 / load TEVA and TRU at same time/remove TRU cart./elute Am % Am-243 Recovery (Electroplating* ) 1) 93.2 2) 92.1 3)107.4 4) 70.3 5)102.4 6)103.0 7)100.2 8)103.3 9)102.6 10)94.7 Avg. =96.9%

20 TRU Resin-U Tracer Recoveries 500 mL urine sample/ U-232 tracer= 0.554 dpm / TRU cartridge after TEVA SA+AA/+NO 2 / load TEVA and TRU at same time/remove TRU cart./elute U % U-232 Recovery (Electroplating* ) 1) 97.9 2) 74.1 3)85.6 4) 102.9 5)90.6 6)83.1 7)57.7 8)81.0 9)80.4 10)93.3 Avg. =84.7%

21 Pu/Sr On TEVA/SR RESIN (URINE)

22 TEVA-Pu/Sr Cartridge Recoveries 500 mL urine sample Sr-90 spiked in samples: 206 dpm Measured dpm % Sr-90 Spike Recovery 171 83.0 17283.5 15575.2 16077.7 17384.0 16077.7 15977.2 Avg 164.379.8 Sr-90 Spiked after precipitation: Measured dpm% Sr-90 Spike Recovery 18489.3% 18891.3% Avg 186 90.3 %

23 Summary New implementation of rapid column methods in bioassay lab will result in significant time/cost savings Pu and Np together with Pu-236 tracer Better Th-228 removal using 2nd 1 mL TEVA col. when U-232 tracer added Pu, Np and Sr on TEVA+Sr cartridge Pu, Np and Am, U on single two stage TEVA-TRU column with Sr-90 on SR Resin after evaporation


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