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一步自组装 Fe-生物炭复合材料增强过硫酸盐活化降解苯酚:不同活性位引发的自由基/非自由基机制。

One-step self-assembly of Fe-biochar composite for enhanced persulfate activation to phenol degradation: Different active sites-induced radical/non-radical mechanism.

机构信息

School of Resources and Environment, Northeast Agricultural University, Harbin, 150030, China.

Heilongjiang Academy of Land Reclamation Sciences, Harbin, 150030, China.

出版信息

Chemosphere. 2023 May;322:138168. doi: 10.1016/j.chemosphere.2023.138168. Epub 2023 Feb 16.

Abstract

Persulfate (PS) activation by nanoscale zerovalent iron (nZVI) is promising for water purification, while is limited due to its easy agglomeration and oxidation. Herein, nZVI encapsuled in carbon matrix shell was synthesized via one-step carbothermal reduction. The core-shell structure effectively inhibited oxidation and agglomeration of nZVI core, and graphitized porous structures facilitated phenol binding with maximal adsorption capacity of 117.10 mg/g achieved by nZVI-BC. Both reactive oxygen species (SO, O•H, O and O) and electron transfer process resulted in phenol decomposition. Owing to diversified active sites, the nZVI-BC/PS system could completely degrade phenol degradation within short time, and exhibited great adaptation to extensive pH range (3.0-9.0) and coexisting substances. Additionally, the nZVI-BC/PS system could maintain over 85% removal of phenol after three recycles or 50 days of storage, and was highly-efficient to different water environments, thus proposing rational design of iron-carbon catalyst with potential in water treatment.

摘要

过硫酸盐(PS)通过纳米零价铁(nZVI)的活化有望用于水净化,但由于其易团聚和氧化而受到限制。本文通过一步碳热还原法合成了封装在碳基质壳中的 nZVI。核壳结构有效地抑制了 nZVI 核的氧化和团聚,而石墨化多孔结构有利于酚类物质的结合,使 nZVI-BC 的最大吸附容量达到 117.10mg/g。活性氧物种(SO、O•H、O 和 O)和电子转移过程均导致了苯酚的分解。由于具有多样化的活性位点,nZVI-BC/PS 体系能够在短时间内完全降解苯酚,并且对广泛的 pH 值范围(3.0-9.0)和共存物质具有很好的适应性。此外,nZVI-BC/PS 体系在三次循环或 50 天储存后仍能保持超过 85%的苯酚去除率,对不同的水环境也具有高效性,因此为水处理中铁-碳催化剂的合理设计提供了思路。

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