Evaluation of materials for iodine and technetium immobilization through sorption and redox-driven processes

被引:34
作者
Pearce, Carolyn I. [1 ]
Cordova, Elsa A. [1 ]
Garcia, Whitney L. [1 ]
Saslow, Sarah A. [1 ]
Cantrell, Kirk J. [1 ]
Morad, Joseph W. [1 ]
Qafoku, Odeta [1 ]
Matyas, Josef [1 ]
Plymale, Andrew E. [1 ]
Chatterjee, Sayandev [1 ]
Kang, Jaehyuk [1 ,7 ]
Colon, Ferdinan Cintron [1 ]
Levitskaia, Tatiana G. [1 ]
Rigali, Mark J. [2 ]
Szecsody, Jim E. [1 ]
Heald, Steve M. [6 ]
Balasubramanian, Mahalingam [6 ]
Wang, Shuao [4 ,5 ]
Sun, Daniel T. [3 ]
Queen, Wendy L. [3 ]
Bontchev, Ranko
Moore, Robert C. [1 ,8 ]
Freedman, Vicky L. [1 ]
机构
[1] Pacific Northwest Natl Lab, 902 Battelle Blvd,POB 999, Richland, WA 99352 USA
[2] Sandia Natl Labs, POB 5800, Albuquerque, NM 87185 USA
[3] EPFL Valais Wallis, Lab Funct Inorgan Mat, CH-1951 Sion, Switzerland
[4] Soochow Univ, Sch Radiol & Interdisciplinary Sci RAD X, State Key Lab Radiat Med & Protect, Suzhou 215123, Peoples R China
[5] Soochow Univ, Collaborat Innovat Ctr Radiat Med, Jiangsu Higher Educ Inst, Suzhou 215123, Peoples R China
[6] Argonne Natl Lab, Adv Photon Source, Argonne, IL 60439 USA
[7] Pohang Univ Sci & Technol, Div Adv Nucl Engn, Pohang, South Korea
[8] BayoTech Inc, Albuquerque, NM USA
关键词
Iodate; Pertechnetate; Iron oxides; layered double hydroxides; Bismuth-based materials; Metal organic frameworks; GROUNDWATER; SEDIMENTS; I-129;
D O I
10.1016/j.scitotenv.2019.136167
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Radioactive iodine-129 (I-129) and technetium-99 (Tc-9(9)) pose a risk to groundwater due to their long half-lives, toxicity, and high environmental mobility. Based on literature reviewed in Moore et al. (2019) and Pearce et aL (2019), natural and engineered materials, including iron oxides, low-solubility sulfides, tin-based materials, bismuth-based materials, organoclays, and metal organic frameworks, were tested for potential use as a deployed technology for the treatment of I-129 and Tc-99 to reduce environmental mobility. Materials were evaluated with metrics including capacity for IO3- and TcO4- uptake, selectivity and long-term immobilization potential. Batch testing was used to determine IO3- and TcO4- sorption under aerobic conditions for each material in synthetic groundwater at different solution to solid ratios. Material association with IO3- and TcO4- was spatially resolved using scanning electron microscopy and X-ray microprobe mapping. The potential for redox reactions was assessed using X-ray absorption near edge structure spectroscopy. Of the materials tested, bismuth oxy(hydroxide) and ferrihydrite performed the best for IO3-. The commercial Purolite A530E anion-exchange resin outperformed all materials in its sorption capacity for TcO4-. Tin-based materials had high capacity for TcO4-, but immobilized TcO4- via reductive precipitation. Bismuth-based materials had high capacity for TcO4-, though slightly lower than the tin-based materials, but did not immobilize TcO4- by a redox-drive process, mitigating potential negative re-oxidation effects over longer time periods under oxic conditions. Cationic metal organic frameworks and polymer networks had high Tc removal capacity, with TcO4- trapped within the framework of the sorbent material. Although organodays did not have the highest capacity for IO3- and TcO4- removal in batch experiments, they are available commercially in large quantities, are relatively low cost and have low environmental impact, so were investigated in column experiments, demonstrating scale-up and removal of IO3- and TcO4- via sorption, and reductive immobilization with iron- and sulfur-based species. (C) 2020 Elsevier B.V. All rights reserved.
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页数:12
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