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Bio- and mineral acid leaching of rare earth elements from synthetic phosphogypsum Paul

作   者:
Antonick, Paul J.Hu, ZhichaoFujita, YoshikoReed, David W.Das, GauravWu, LiliShivaramaiah, RadhaKim, PaulEslamimanesh, AliLencka, Malgorzata M.Jiao, YongqinAnderko, AndrzejNavrotsky, AlexandraRiman, Richard E.
作者机构:
Lawrence Livermore Natl Lab Phys & Life Sci DirectorateOLI Syst IncUniv Calif DavisRutgers State Univ Mat Sci & EngnSuite 301 Cedar Knolls 607 Taylor Rd ID 83415 USA Biosci & Biotechnol Div Idaho Falls Davis Piscataway CA 95616 USA CA 94550 USA NJ 08854 USA LivermoreIdaho Natl Lab Peter A Rock Thermochem Lab Biol & Chem Proc Dept 240 Cedar Knolls Rd NJ 07927 USA
关键词:
BioleachingRare earth recoveryBiohydrometallurgyMineral acid leaching
期刊名称:
The Journal of Chemical Thermodynamics
i s s n:
0021-9614
年卷期:
2019 年 132 卷
页   码:
491-496
页   码:
摘   要:
Leaching of six individual rare earth (yttrium, cerium, neodymium, samarium, europium, and ytterbium) doped synthetic phosphogypsum samples using a suite of lixiviants was conducted. The lixiviants chosen for this study were phosphoric acid, sulfuric acid, gluconic acid, and a "biolixiviant" consisting of spent medium containing organic acids from the growth of the bacterium Gluconobacter oxydans on glucose. The biolixiviant had a pH of 2.1 and the dominant organic acid was determined to be gluconic acid, present at a concentration of 220 mM. The leaching behaviors of the studied lixiviants were compared and rationalized by thermodynamic simulations. The results suggest that at equivalent molar concentrations of 220 mM the biolixiviant was more efficient at rare earth element (REE) extraction than gluconic acid and phosphoric acid but less efficient than sulfuric acid. Unlike the organic acids, at pH 2.1 the mineral acids failed to extract REE, likely due to different complexation and kinetic effects. (C) 2019 Elsevier Ltd.
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