降级(电信)
污染物
钴
碳纳米管
环境化学
化学工程
化学
碳纤维
总有机碳
材料科学
无机化学
纳米技术
有机化学
计算机科学
复合材料
电信
复合数
工程类
作者
Juan Yang,Lei Zhao,Yuxing Sun,Zilong Zhang,Sheng Wang,Guangming Zhou,Jingdong Peng
标识
DOI:10.1016/j.jwpe.2024.105910
摘要
By confining the metal nanoparticles within the carbon nanotubes, it is feasible to inhibit their aggregation and leaching while preserving their catalytic activity. In this study, a low cobalt leaching nanomaterial (Co@CNT-3) was developed using cobalt nanoparticle-modified carbon nanotubes (CNTs) derived from a porous morphology-controlled imidazolate molecular sieve framework (ZIF-67). This nanomaterial effectively activates PMS for the efficient degradation of organic pollutants. In this unique structure, exhibited excellent catalytic activity due to the synergistic interaction between ZIF-67-derived Co NPs and CNT-3. The removal of methylene blue (MB) reached >99 % within 20 min after the addition of peroxomonosulfate (PMS) and showed good catalytic activity in a wide pH range (3.0–11.0) and common anions (Cl− SO42− H2PO4− HCO3−) in the aqueous environment. The cobalt ion leaching rate of Co@CNT-3 in solution is only 0.01 mg/L. Through X-ray photoelectron spectroscopy (XPS), quenching and electron paramagnetic resonance (EPR) experiments, it was found that Co nanoparticles are the main catalytic active center, and a non-radical mechanism dominated by singlet oxygen (1O2) is proposed. This study provides a simple strategy for the synthesis of high-efficiency catalysts with low cobalt ion leaching.
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