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核壳普鲁士蓝类似物@聚间苯二胺作为高效过一硫酸盐活化剂用于降解罗丹明 B,同时减少金属浸出。

Core-shell Prussian blue analogues@ poly(m-phenylenediamine) as efficient peroxymonosulfate activators for degradation of Rhodamine B with reduced metal leaching.

机构信息

School of Resource and Environmental Science, Key Laboratory for Biomass-Resource Chemistry and Environmental Biotechnology of Hubei Province, Wuhan University, Wuhan 430072, PR China.

School of Resource and Environmental Science, Key Laboratory for Biomass-Resource Chemistry and Environmental Biotechnology of Hubei Province, Wuhan University, Wuhan 430072, PR China.

出版信息

J Colloid Interface Sci. 2019 Jan 15;534:586-594. doi: 10.1016/j.jcis.2018.09.074. Epub 2018 Sep 22.

Abstract

Herein, Prussian blue analogues@poly(m-phenylenediamine) nanoparticles (PBA@PmPDs) with well-defined core-shell structure were synthesized. The successful coating of poly(m-phenylenediamine) (PmPD) on the surface of FeCo [Co(CN)] (Fe-Co-Co PBA) was confirmed by SEM, TEM, XRD, TGA, FT-IR and XPS. The catalytic performance of Fe-Co-Co PBA@PmPDs was evaluated by activation of peroxymonosulfate (PMS) for degradation of Rhodamine B (RhB), the effects of different influence factors on the RhB degradation efficiency were investigated, including PMS concentration, temperature, initial solution pH, and co-existing inorganic salts. Cobalt ions leaching and stability of the catalysts were studied, Co ions concentration dissolved into the solution from the solid catalysts at 60 min is reduced by half after the Fe-Co-Co PBA is coated with PmPDs. The RhB removal efficiency is higher than 90% even after four cycles and the nanoparticles still maintain the core-shell structure, indicating that Fe-Co-Co PBA@PmPDs is stabile and reusable. Radical quenching experiments and electron paramagnetic resonance spectra indicate that both SO and OH are generated during the PMS activation process and SO is the dominant reactive species. In virtue of its superior catalytic activity, excellent reusability and stability, low metallic ion leaching, Fe-Co-Co PBA@PmPDs could be a promising catalyst for the remediation of contaminated water.

摘要

本文合成了具有明确核壳结构的普鲁士蓝类似物@聚间苯二胺纳米粒子(PBA@PmPDs)。SEM、TEM、XRD、TGA、FT-IR 和 XPS 证实了成功地在 FeCo[Co(CN)](Fe-Co-Co PBA)表面包覆了聚间苯二胺(PmPD)。通过活化过一硫酸盐(PMS)降解罗丹明 B(RhB)评估了 Fe-Co-Co PBA@PmPDs 的催化性能,研究了不同影响因素对 RhB 降解效率的影响,包括 PMS 浓度、温度、初始溶液 pH 值和共存无机盐。研究了钴离子浸出和催化剂的稳定性,Fe-Co-Co PBA 包覆 PmPDs 后,60 分钟内从固相中溶解到溶液中的 Co 离子浓度降低了一半。即使经过四个循环,RhB 的去除效率仍高于 90%,并且纳米粒子仍保持核壳结构,表明 Fe-Co-Co PBA@PmPDs 稳定且可重复使用。自由基猝灭实验和电子顺磁共振谱表明,在 PMS 活化过程中同时生成了 SO 和 OH,并且 SO 是主要的反应性物质。由于其优异的催化活性、良好的可重复使用性和稳定性、低金属离子浸出率,Fe-Co-Co PBA@PmPDs 可能是一种有前途的受污染水修复催化剂。

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