Uranium In Situ Electrolytic Deposition with a Reusable Functional Graphene-Foam Electrode

被引:100
作者
Wang, Chao [1 ,2 ]
Helal, Ahmed S. [1 ,3 ]
Wang, Ziqiang [1 ]
Zhou, Jian [1 ]
Yao, Xiahui [1 ]
Shi, Zhe [1 ]
Ren, Yang [4 ]
Lee, Jinhyuk [1 ]
Chang, Jeng-Kuei [5 ]
Fugetsu, Bunshi [6 ]
Li, Ju [1 ,7 ]
机构
[1] MIT, Dept Nucl Sci & Engn, Cambridge, MA 02139 USA
[2] Tongji Univ, Sch Mat Sci & Engn, Shanghai 201804, Peoples R China
[3] Nucl Mat Author, POB 540, Cairo, Egypt
[4] Argonne Natl Lab, Adv Photon Source, 9700 South Cass Ave, Lemont, IL 60439 USA
[5] Natl Chiao Tung Univ, Dept Mat Sci & Engn, Hsinchu 30010, Taiwan
[6] Univ Tokyo, Inst Future Initiat, Bunkyo Ku, Tokyo 1130032, Japan
[7] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
关键词
electrolytic deposition; extraction capacity; graphene foam; local pH; nuclear energy; reusability; uranium extraction; X-RAY PHOTOELECTRON; INFRARED-SPECTRA; DRINKING-WATER; REMOVING URANIUM; OXIDE; XPS; GROUNDWATER; CATHODE; NUN;
D O I
10.1002/adma.202102633
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nuclear fission produces 400 GWe which represents 11% of the global electricity output. Uranium is the essential element as both fission fuel and radioactive waste. Therefore, the recovery of uranium is of great importance. Here, an in situ electrolytic deposition method to extract uranium from aqueous solution is reported. A functionalized reduced graphene oxide foam (3D-FrGOF) is used as the working electrode, which acts as both a hydrogen evolution reaction catalyst and a uranium deposition substrate. The specific electrolytic deposition capacity for U(VI) ions with the 3D-FrGOF is 4560 mg g(-1) without reaching saturation, and the Coulombic efficiency can reach 54%. Moreover, reduction of the uranium concentration in spiked seawater from 3 ppm to 19.9 ppb is achieved, which is lower than the US Environmental Protection Agency uranium limits for drinking water (30 ppb). Furthermore, the collection electrode can be efficiently regenerated and recycled at least nine times without much efficiency fading, by ejecting into 2000 ppm concentrated uranium solution in a second bath with reverse voltage bias. All these findings open new opportunities in using free-standing 3D-FrGOF electrode as an advanced separation technique for water treatment.
引用
收藏
页数:11
相关论文
共 53 条
[1]   Recent advances in nuclear power: A review [J].
Abu-Khader, Mazen M. .
PROGRESS IN NUCLEAR ENERGY, 2009, 51 (02) :225-235
[2]   STUDIES ON THE HYDROLYSIS OF METAL IONS .10. THE HYDROLYSIS OF THE URANYL ION, UO22+ [J].
AHRLAND, S ;
HIETANEN, S ;
SILLEN, LG .
ACTA CHEMICA SCANDINAVICA, 1954, 8 (10) :1907-1916
[3]   Infrared Spectra and Electronic Structure Calculations for NN Complexes with U, UN, and NUN in Solid Argon, Neon, and Nitrogen [J].
Andrews, Lester ;
Wang, Xuefeng ;
Gong, Yu ;
Kushto, Gary P. .
JOURNAL OF PHYSICAL CHEMISTRY A, 2014, 118 (28) :5289-5303
[4]  
[Anonymous], UR MIN OV UPD DEC 20
[5]   Introduction of amino groups into acid-resistant MOFs for enhanced U(VI) sorption [J].
Bai, Zhi-Qiang ;
Yuan, Li-Yong ;
Zhu, Lin ;
Liu, Zhi-Rong ;
Chu, Sheng-Qi ;
Zheng, Li-Rong ;
Zhang, Jing ;
Chai, Zhi-Fang ;
Shi, Wei-Qun .
JOURNAL OF MATERIALS CHEMISTRY A, 2015, 3 (02) :525-534
[6]   Performance of three resin-based materials for treating uranium-contaminated groundwater within a PRB [J].
Barton, CS ;
Stewart, DI ;
Morris, KS ;
Bryant, DE .
JOURNAL OF HAZARDOUS MATERIALS, 2004, 116 (03) :191-204
[7]   IMPROVED TETRAHEDRON METHOD FOR BRILLOUIN-ZONE INTEGRATIONS [J].
BLOCHL, PE ;
JEPSEN, O ;
ANDERSEN, OK .
PHYSICAL REVIEW B, 1994, 49 (23) :16223-16233
[8]   Highly porous and stable metal-organic frameworks for uranium extraction [J].
Carboni, Michael ;
Abney, Carter W. ;
Liu, Shubin ;
Lin, Wenbin .
CHEMICAL SCIENCE, 2013, 4 (06) :2396-2402
[9]   The application of iron-based technologies in uranium remediation: A review [J].
Chen, Anwei ;
Shang, Cui ;
Shao, Jihai ;
Zhang, Jiachao ;
Huang, Hongli .
SCIENCE OF THE TOTAL ENVIRONMENT, 2017, 575 :1291-1306
[10]   THE INFRA-RED SPECTRA AND STRUCTURES OF SOME HYDRATED URANIUM TRIOXIDES AND AMMONIUM DIURANATES [J].
DEANE, AM .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1961, 21 (3-4) :238-252