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在温和条件下,无贵金属的 Cu/TiO 纳米复合材料上超快速和深度脱溴四溴二苯醚。

Ultrarapid and Deep Debromination of Tetrabromodiphenyl Ether over Noble-Metal-Free Cu/TiO Nanocomposites under Mild Conditions.

机构信息

Key Laboratory of Catalysis and Materials Science of the State Ethnic Affairs Commission and Ministry of Education, College of Resources and Environmental Science , South-Central University for Nationalities , Wuhan 430074 , People's Republic of China.

School of Chemistry and Chemical Engineering , Huazhong University of Science and Technology , Wuhan 430074 , People's Republic of China.

出版信息

Environ Sci Technol. 2018 Oct 16;52(20):11743-11751. doi: 10.1021/acs.est.8b03202. Epub 2018 Sep 27.

Abstract

Fast and deep debromination of polybrominated diphenyl ethers (PBDEs) under mild conditions is a challenge in the field of pollution control. A strategy was developed to achieve it by exploiting Cu/TiO composites as a noble-metal-free catalyst. Toward the debromination of 2,2',4,4'-tetrabromodiphenyl ether (BDE47) as a typical PBDE, the use of Cu/TiO as a catalyst and hydrazine hydrate (NH·HO) as a reducing agent yielded a degradation removal of 100% and a debromination efficiency of 87.7% in 3 s. A complete debromination of BDE47 at 1500 mg L was possible by successively adding NH·HO. A debromination pathway involving active H atom species was proposed for the catalytic transfer hydrogenation (CTH) of PBDEs according to the identified degradation intermediates. A mechanism was further clarified by density functional theory calculations: electrons are delivered from NH·HO to the metallic Cu atom via a coordination of N in NH·HO with Cu atoms. The electron-trapped Cu atom interacts with adsorbed BDE47 to form a transition complex, and then the debromination of this complex occurs on the surface of Cu nanoparticles due to the hydrogen donation of NH·HO through the CTH process. The new method provides a highly efficient method to remove brominated pollutants.

摘要

在温和条件下快速深度脱溴多溴二苯醚(PBDEs)是污染控制领域的一个挑战。通过利用 Cu/TiO 复合材料作为无贵金属催化剂来开发一种实现这一目标的策略。在以 2,2',4,4'-四溴二苯醚(BDE47)作为典型 PBDE 的脱溴研究中,使用 Cu/TiO 作为催化剂和水合肼(NH·HO)作为还原剂,在 3 秒内实现了 100%的降解去除率和 87.7%的脱溴效率。通过连续添加 NH·HO,可以在 1500 mg L 的条件下实现 BDE47 的完全脱溴。根据鉴定出的降解中间体,提出了一种涉及活性 H 原子物种的催化转移氢化(CTH)脱溴途径。通过密度泛函理论计算进一步阐明了机理:电子通过 NH·HO 中的 N 与 Cu 原子的配位从 NH·HO 传递到 Cu 原子。电子捕获的 Cu 原子与吸附的 BDE47 相互作用形成过渡复合物,然后由于 NH·HO 通过 CTH 过程提供氢,该复合物在 Cu 纳米颗粒表面发生脱溴。该新方法提供了一种高效去除溴化污染物的方法。

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