迈向可持续电池回收:模型系统中氨基聚羧酸衍生物配体中镍(II)和钴(II)的选择性解吸

IF 1.5 4区 工程技术 Q3 ENGINEERING, CHEMICAL
M.Sc. Björn Robeck, M.Sc. Katharina Hoff, Dr. Helena Horn
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引用次数: 0

摘要

除其他外,由于对锂离子电池的高需求,所需的临界重金属已成为稀缺资源。因此,能够回收这些材料的有效的再循环过程是非常重要的。采用氨基聚羧酸衍生物配体功能化二氧化硅吸附剂(HSU331)选择性吸附镍(II)和钴(II)。随后,研究了变ph解吸的适宜参数。Co(II)的最大解吸效率在pH = 2.7时达到72%,Ni(II)在pH = - 0.5时达到94%。利用这些结果设计了一种ph移位解吸工艺,以选择性地回收Co(II),并在同时吸附Co(II)和Ni(II)后再生吸附剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Towards Sustainable Battery Recycling: Selective Desorption of Nickel(II) and Cobalt(II) from Amino-Polycarboxylate Derivate Ligands in Model Systems

Towards Sustainable Battery Recycling: Selective Desorption of Nickel(II) and Cobalt(II) from Amino-Polycarboxylate Derivate Ligands in Model Systems

Inter alia due to the high demand for lithium-ion batteries, the required critical heavy metals have become a scarce resource. Consequently, effective recycling processes that enable the recovery of such materials are of high interest. A silica adsorbent functionalized with amino-polycarboxylate derivate ligands (HSU331) was applied in order to selectively adsorb nickel(II) and cobalt(II). Subsequently, suitable parameters for a pH-swing desorption were investigated. Maximum desorption efficiencies for Co(II) were achieved at pH = 2.7 (72 %) and for Ni(II) at pH = −0.5 (94 %). These results were used for the design of a pH-shift desorption process in order to selectively recover Co(II) and regenerate the adsorbent after simultaneous adsorption of Co(II) and Ni(II).

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来源期刊
Chemie Ingenieur Technik
Chemie Ingenieur Technik 工程技术-工程:化工
CiteScore
3.40
自引率
15.80%
发文量
601
审稿时长
3-6 weeks
期刊介绍: Die Chemie Ingenieur Technik ist die wohl angesehenste deutschsprachige Zeitschrift für Verfahrensingenieure, technische Chemiker, Apparatebauer und Biotechnologen. Als Fachorgan von DECHEMA, GDCh und VDI-GVC gilt sie als das unverzichtbare Forum für den Erfahrungsaustausch zwischen Forschern und Anwendern aus Industrie, Forschung und Entwicklung. Wissenschaftlicher Fortschritt und Praxisnähe: Eine Kombination, die es nur in der CIT gibt!
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