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采用组合方法提高亚硝基 - R - 盐在智能手机电池锂生物浸出回收中测定Co(II)的选择性。

Enhancing the Selectivity of Nitroso-R-Salt for the Determination of Co(II) in Lithium Bioleaching Recovery of Smartphone Batteries Using a Combinatorial Methodology Approach.

作者信息

Ricart David, Dorado Antonio David, Baeza Mireia, Lao-Luque Conxita

机构信息

Department of Mining, Industrial and ICT Engineering, Escola Politècnica Superior d'Enginyeria de Manresa, Universitat Politècnica de Catalunya, Avinguda de les Bases de Manresa 61-73, 08240 Manresa, Spain.

GENOCOV Research Group, Department of Chemistry, Faculty of Science, Edifici C-Nord, Universitat Autònoma de Barcelona, Carrer dels Til·lers, 08193 Bellaterra, Spain.

出版信息

Nanomaterials (Basel). 2025 Aug 16;15(16):1264. doi: 10.3390/nano15161264.

Abstract

The selectivity of the colorimetric method for Co(II) determination using the nitroso-R-salt (NRS) in samples with complex matrices has been improved. Interferences caused by Cu(II), Fe(II), Fe(III), Mn(II), Al(III) and Ni(II) ions, which were present in the bioleach ate of lithium-ion batteries, have been solved through the sequential addition of masking agents: acetate, fluoride, ethylenediaminetetraacetic acid (EDTA), and strong acids (HSO). The absorbance of the NRS-Co(II) complex was typically measured at 525 nm, but it was also studied at 550 nm due to minimal interferences observed at 550 nm. The sequence of the masking agent's addition showed a significant influence on the interference effect. The optimal sequence was sample, acetate-acetic acid buffer solution with dissolved fluoride, NRS, EDTA and HSO. The proposed method demonstrated robust performance at 550 nm, with a relative standard deviation (RSD) around 2%, and good accuracy (RV% around 100%). The limit of detection (LoD) was 0.1 mg L and the limit of quantification (LoQ) was 0.3 mg L. The linear range extended up to 15 mg L (R = 0.998). Real samples analyzed using the optimized method showed no significant differences when compared to results from atomic absorption spectroscopy, confirming its reliability.

摘要

使用亚硝基 - R - 盐(NRS)测定复杂基质样品中钴(II)的比色法的选择性得到了提高。通过依次添加掩蔽剂:乙酸盐、氟化物、乙二胺四乙酸(EDTA)和强酸(HSO),解决了锂离子电池生物浸出液中存在的铜(II)、铁(II)、铁(III)、锰(II)、铝(III)和镍(II)离子引起的干扰。NRS - 钴(II)络合物的吸光度通常在525 nm处测量,但由于在550 nm处观察到的干扰最小,也在550 nm处进行了研究。掩蔽剂添加顺序对干扰效果有显著影响。最佳顺序是样品、含有溶解氟化物的乙酸盐 - 乙酸缓冲溶液、NRS、EDTA和HSO。所提出的方法在550 nm处表现出稳健的性能,相对标准偏差(RSD)约为2%,准确度良好(回收率约为100%)。检测限(LoD)为0.1 mg/L,定量限(LoQ)为0.3 mg/L。线性范围扩展至15 mg/L(R = 0.998)。使用优化方法分析的实际样品与原子吸收光谱法的结果相比没有显著差异,证实了其可靠性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3815/12389291/cc5fe107ea67/nanomaterials-15-01264-g001.jpg

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