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Highly selective capture of palladium from acidic solution by sulfur-functionalized porous carbon microspheres: performance and mechanism
Environmental Science: Nano ( IF 5.8 ) Pub Date : 2024-11-15 , DOI: 10.1039/d4en00738g
Mingyue Wang, Ruiwen Liang, Lanchao Kou, Xiukun Cao, Dezhi Chen

Efficient recovery of palladium (Pd) from waste sources is of paramount importance due to its limited natural reserves and potential environmental hazards. Herein, a carbon sorbent, namely sulfur-functionalized porous carbon microspheres (SPCMs), was used to selectively capture Pd(II) from acidic solution. SPCMs exhibited high efficiency for the adsorption separation of Pd(II) from 0.5 M to 6 M HNO3 solution. The adsorption kinetics of Pd(II) matched well with the pseudo-second-order model. The adsorption reached equilibrium after 130 minutes and the adsorption capacity of Pd(II) was 79.3 mg g−1 in 1 M HNO3 solution. The Freundlich isotherm model exhibited a better description of the Pd(II) adsorption, suggesting that the Pd(II) adsorption is a multilayer adsorption process. SPCMs showed a high selectivity for the capture of Pd(II) in simulated acidic wastewater with 26 metal ions, and the selectivity increased with the increase of HNO3 concentration. The adsorption capacity per US dollar of Pd(II) by SPCMs from HNO3 solution is much higher than those of previously reported sorbents, exhibiting a high economic viability of SPCMs for Pd(II) capture from acidic solution. The adsorbed Pd(II) could be desorbed using 1.0 M thiourea and 0.1 M HNO3, and the SPCM sorbent maintained a high adsorption capacity after five adsorption–desorption cycles. Characterization and theoretical calculations revealed that the adsorption of Pd(II) on the SPCM sorbent is dominated by the coordination of [Pd(NO3)2] with O/S containing groups and some of the Pd(II) is reduced to Pd(0). The excellent adsorption performance of SPCMs provides a feasible and low-cost strategy for the selective recovery of Pd(II) from acidic wastewater.

中文翻译:


硫功能化多孔碳微球从酸性溶液中高选择性捕获钯:性能与机理



由于钯 (Pd) 的自然储量有限且存在潜在的环境危害,因此从废物源中有效回收钯 (Pd) 至关重要。在此,使用碳吸附剂,即硫官能化多孔碳微球 (SPCM) 从酸性溶液中选择性捕获 Pd(II)。SPCM 对 0.5 M 至 6 M HNO3 溶液中 Pd(II) 的吸附分离表现出高效率。Pd(II) 的吸附动力学与准二级模型匹配良好。吸附在 130 分钟后达到平衡,Pd(II) 在 1 M HNO3 溶液中的吸附容量为 79.3 mg g-1。Freundlich 等温线模型对 Pd(II) 吸附表现出更好的描述,表明 Pd(II) 吸附是一个多层吸附过程。SPCMs 对 26 个金属离子模拟酸性废水中 Pd(II) 的捕获表现出高选择性,并且选择性随着 HNO3 浓度的增加而增加。SPCM 从 HNO3 溶液中吸附每美元 Pd(II) 的容量远高于以前报道的吸附剂,表现出 SPCM 从酸性溶液中捕获 Pd(II) 的高经济可行性。吸附的 Pd(II) 可以使用 1.0 M 硫脲和 0.1 M HNO3 进行解吸,并且 SPCM 吸附剂在 5 次吸附-解吸循环后仍保持较高的吸附容量。 表征和理论计算表明,Pd(II) 在 SPCM 吸附剂上的吸附主要由 [Pd(NO32] 与含有 O/S 的基团的配位决定,并且一些 Pd(II) 被还原为 Pd(0)。SPCMs 优异的吸附性能为从酸性废水中选择性回收 Pd(II) 提供了一种可行且低成本的策略。
更新日期:2024-11-15
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