Application of Rapid and Automated Techniques in Radiochemical Analysis ---Inspirations from NKS-B Rapid-Tech Project. Jixin Qiao

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Application of Rapid and Automated Techniques in Radiochemical Analysis ---Inspirations from NKS-B Rapid-Tech Project Jixin Qiao

NKS-B Rapid-tech project [AFT/B(14)7] Funded by Nordic Nuclear Safety Research (NKS) for 2014-2016 Partners: Jixin Qiao, Kai Xu---DTU Nutech, Technical University of Denmark, Denmark Petra Lagerkvist, Sofia Josson, Stina Holmgren---FOI, CBRN Defence and Security, Sweden Rajdeep Singh Sidhu---IFE, Institute for Energy Technology, Norway Iisa Outola, Pia Vesterbacka, Kaisa Vaaramaa---STUK, Radiation and Nuclear Safety Authority, Finland 2

Project objectives To explore the application of different rapid techniques in determination of radionuclides, thus to improve the analytical efficiency of present radioanalytical methods in the areas of E, W and R. Specific tasks: Identification of current needs and problems in methodology development for rapid determination of 90 Sr and actinides. Identification of individual processes wherein rapid techniques can be potentially applied to improve the analytical efficiency. 3

Our focus No. Rapid techniques 1 Flow injection (FI)/sequential injection (SI) 2 High performance liquid chromatography (HPLC) 3 Vacuum box system 4 On-line detection (FI-ICPMS, HPLC-ICPMS) 5 other effective sample treatment approaches (microwave assisted digestion, alkaline fusion, co-precipitation) 4

Rapid radiochemical analysis Flow/sequential injection chromatographic separation: Flow injection (FI) system: Peristaltic pump Continuous flow Fig. Scheme of a FI system Sequential injection (SI) system: Syringe pump Selection valve Fig. Scheme of a SI system 5

Our focus No. Rapid techniques 1 Flow injection (FI)/sequential injection (SI) 2 High performance liquid chromatography (HPLC) 3 Vacuum box 4 On-line detection (FI-ICPMS, HPLC-ICPMS) 5 other effective sample treatment approaches (microwave assisted digestion, alkaline fusion, co-precipitation) 6

Rapid radiochemical analysis High performance liquid chromatography (HPLC): Advantages: Fully automated Can be connected directly with MS Disadvantages: Only handle small samples Single sample processing High cost HPLC system 7

Our focus No. Rapid techniques 1 Flow injection (FI)/sequential injection (SI) 2 High performance liquid chromatography (HPLC) 3 Vacuum box system 4 On-line detection (FI-ICPMS, HPLC-ICPMS) 5 other effective sample treatment approaches (microwave assisted digestion, alkaline fusion, co-precipitation) 8

Rapid radiochemical analysis Vaccum box: Advantages: Multi-sample processing Easy operation Low cost Flexible Disadvantages: Need human attention Eichrom vaccum box 9

Our focus No. Rapid techniques 1 Flow injection (FI)/sequential injection (SI) 2 High performance liquid chromatography (HPLC) 3 Vacuum box system 4 On-line detection (FI-ICPMS, HPLC-ICPMS) 5 other effective sample treatment approaches (microwave assisted digestion, alkaline fusion, co-precipitation) 10

Rapid radiochemical analysis Alkaline fusion --- Rapid sample pre-treatment techniques for solid samples: Fluxes can be used for alkaline fusion: NaOH Na 2 O 2 NaCO 3 LiBO 2 Others Katanax automatic electric fluxer Busen burner 11

Rapid radiochemical analysis Co-precipitation --- Rapid sample pre-treatment for liquid samples: Carbonates (e.g.,caco 3 ) Oxalates (e.g., CaC 2 O 4 ) Hydroxides (e.g., Fe(OH) 3 ) Oxides (e.g., MnO 2 ) Phosphates (e.g., Ca 3 (PO 4 ) 2, BiPO 4 ) Others (e.g., AMP for Cs) Fe(OH) 3 co-precipitation CaCO 3 co-precipitation CaC 2 O 4 co-precipitation 12

NKS-B Rapid-tech project 2014-2015 Current analytical methods for Sr and actinides were screened among participating institutes. Conclusions: 1) Current application of novel automated techniques in Nordic countries is very limited. 2) There is a need for end users to become more aware of the advantages of improved techniques for radiochemical assays. Example: 90 Sr determination for 45 L seawater (DTU-Nutech routine analysis) 13

Pre-concentration and preliminary Ca removal 45 L seawater Add 85 Sr tracer and 1g SrCl 2 H 2 O Adjust ph to 8-10 with 25% NH 3 H 2 O.Heat to boiling. Add 40 ml 25% HN 3 H 2 O and 1-1.5 L 2 M (NH 4 ) 2 CO 3. Stir with stick and stand overnight 15-20 hr SrCO 3 Precipitate Dissolve with 1 L of 4 M HNO 3. Wash the container with 0.5 L of H 2 O twice. Add 10 mg of Fe 3+. Heat to boiling. Add 250-300 ml 6 M NaOH to ph=10, then add 350 ml 6 M NaOH to 0.2 M NaOH and centrifuge. Heat to boiling. Add Na 2 CO 3 to 50g/L. Stir and heat under 250 C for 1h. Stay overnight and centrifuge Supernatant SrCO 3 precipitate 3-5 hr 15-20 hr Total: 2 d 14

Further Ca removal and purification Add 4 ml 8 M HNO 3 to dissolve the sample. Add 150 ml 65% HNO 3 and 30 ml of fuming HNO 3 and centrifuge. Add 4 ml water, 60 ml 65% HNO 3 and 15 ml of fuming HNO 3 and centrifuge. Repeat two times. Dissolve the precipitate in 50 ml water, add 5 mg Fe 3+ and NaOH to ph=10, centrifuge. SrCO 3 precipitate Sr(NO 3 ) 2 precipitate Sr(NO 3 ) 2 precipitate 3-5 hr Supernatant Add Y 3+ carrier and 1 mg Ba carrier, take a part of the solution to measure by NaI detector for Sr chemical yield. Stand over 3 weeks for the in-growth of Y. Sr-Y solution 0.5-1 hr + 3 weeks Total: 1 d + 3 w 15

Y purification Sr-Y solution Add 25% NH 3 H 2 O to ph>10, heat for a while and centrifuge. Supernatant Precipitate 3-5 hr > 24 hr Acidify and evaporate to certain volume for storage GM beta counting for 90 Y Total: 16 DTU 2 dnutech, Technical University of Denmark Dissolve with 20 ml 0.7 M HNO 3, Add 5 mg Sr carrier and 25% NH 3 H 2 O to ph>10, centrifuge. Supernatant Dissolve with 20 ml 0.3 M HNO 3. Add 5 mg Ba 2+ and 2 mg Sr 2+ carrier, add 1 ml 2 M H 2 SO 4, centrifuge. Precipitate Supernatant 25% NH 3 H 2 O to ph>10, centrifuge. Repeat the BaSO 4 and Y(OH) 3 precipitation Y(OH) 3 Precipitate Add 5 drops 6 M HNO 3 and 20 ml 8% H 2 C 2 O 4, stir and heat. Filter the Y 2 (C 2 O 4 ) 3 and wash with 2 ml water and alchol for two times. Y 2 (C 2 O 4 ) 3 Precipitate

Performance evaluation and potential improvement Advantages Robust, high applicability, high precision and accuracy, relatively low LOD (5 mbq) Disadvantage Item Detailed problem Possible solution Low safety factor Low efficiency (Analytical turnover >5 days excluding 3-week ingrowth of 90Y ) highly toxic chemical (NH 4 ) 2 CO 3 noxious and corrosive fuming nitric Repeated Sr(NO 3 ) 2 precipitation Long waiting time for 90 Y ingrowth CaC 2 O 4 co-precipitation, room temp. Repeated application of NaOH for removal of Ca Application of Sr resin Direct counting of 90 Sr by LSC High labor intensity Manual operation Flow/sequential injection 17

Sequential injection unit HC R1 R2 R3 R4 SV-1 S1 S2 1 S3 2 10 3 9 S4 4 5 SV-2 8 S5 7 WS 6 AIR S6 R6 R5 S9 S8 S7 3 4 1 2 5 SV-3 6 10 9 8 7 SP 1 2 3 4 5 6 7 8 9 Chromatographic columns Carrier (H 2 O) 2 3 4 5 1 10 SV-4 9 6 8 7 EF1 EF2 1 EF3 2 10 3 SV-5 WS 9 EF4 EF9 4 8 EF5 EF8 5 7 6 EF7 EF6 Automatically handle 9 samples! Work overnight! Qiao, J. X., Hou, X. L., Roos, P., Miró, M. Analytica Chimic Acta. 2011. 18

Flow injection unit PP S2 S1 R1 R2 R3 R4 R8 SV-1 R5 WS AIR R7 R6 S3 S4 1 2 3 4 Columns WS WS WS WS E3 E4 E1 E2 Simultaneously handle 4 samples! Qiao, J. X., Shi, K. L., Hou, X. L., Nielsen, S., Roos, P. Environmental Science & Technology. 2013. 19

Conclusions More efforts are needed to improve the application of automated and rapid techniques in radiochemical analysis More support from NKS or other foundations for future projects More communication and collaboration among Nordic and international labs 20

Thank you! 21