锰
浸出(土壤学)
化学
冶金
无机化学
材料科学
地质学
土壤科学
土壤水分
作者
Zhiyuan Zeng,Bin Li,Yuntao Zheng,Jiehui Hu,Peng Li,Dianwen Liu,Shengming Xu
标识
DOI:10.1002/ange.202514318
摘要
Abstract Silver is an increasingly scarce resource, necessitating green leaching methods for low‐grade ores. Conventional cyanidation, however, suffers from extreme toxicity and environmental hazards that make it unsustainable. We report a nontoxic synergistic leaching system based on oxalic acid and cyano‐functionalized branched quaternary ammonium salts. Under mild conditions, this one‐step method enables efficient and selective leaching of lattice‐confined silver from polymetallic manganese–silver ore, with recoveries exceeding 90%. Kinetic studies reveal a two‑stage process, with an initial rapid dissolution of exposed manganese oxides releasing silver followed by a slower breakdown of the iron matrix to liberate encapsulated minerals. The core breakthrough is the discovery that AgCl combines with chloride anions from the quaternary ammonium salt to form a unique inorganic helical chain structure. The stability of this helical assembly is attributed to an ordered CH…Cl − H‐bonded network. Spectroscopic characterization and theoretical calculations confirm that this network undergoes an energetically favorable reconstruction that overcomes the high lattice energy of AgCl. This finding demonstrates that the cooperative effect of weak H‐bonds can dissociate covalently stabilized solids. Our study thus provides an innovative strategy for sustainable silver metallurgy and introduces a new paradigm of H‐bond‐directed metallurgical design.
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