School of Environmental & Chemical Engineering, Dalian Jiaotong University, Dalian, 116021, China.
School of Environmental & Chemical Engineering, Dalian Jiaotong University, Dalian, 116021, China; Key Lab of Eco-restoration of Regional Contaminated Environment (Shenyang University), Ministry of Education, Shenyang, 110003, China.
Environ Pollut. 2024 Dec 15;363(Pt 1):125050. doi: 10.1016/j.envpol.2024.125050. Epub 2024 Oct 4.
The inherent properties of exposed facets of iron minerals played key roles in heterogeneous reactions at the mineral interface, and the addition of co-catalysts has been elucidated to further enhance the reactions for contaminants degradation. Here, synergistic Fenton-like catalytic reactivity of different hematite dominant exposed facets ({001}, {012}, {100}, and {113}) with nano boron carbide (BC) was revealed. In 5 h, as compared with the cumulative •OH in the BC/HO system (96.9 μM), while that in the {001}/BC/HO system was decreased by 19.6%, those in the {012}/BC/HO, {100}/BC/HO, and {113}/BC/HO systems were increased by 53.8%, 75.9%, and 84.0%, respectively. Significantly, {113}/BC/HO system exhibited strong capability for degradation of a broad spectrum of organic pollutants, including typical phenol, endocrine disruptor (bisphenol A), antibiotic (sulfanilamide), dyes (Rhodamine B and methylene blue), and pesticide (atrazine). During the Fenton-like reactions, higher synergy factor, Fe(III)/Fe(II) cycling rate, and amount of Fe-O-B bond in the {113}/BC/HO system were shown than those in other systems, thus exhibiting its desirable catalytic performance for •OH production and pollutants oxidation. Iron species and X-ray photoelectron spectroscopy (XPS) analyses indicated that B-B bond and interfacial suboxide boron (e.g., B-O) could provide electrons to facilitate Fe(III) reduction for boosting the Fe(III)/Fe(II) cycling. Density functional theory (DFT) results demonstrated the formation of Fe-O-B bond on hematite {113}, {100}, and {012} facets, which were beneficial to the breakage of O-O bond of bound HO molecule and thus improved the generation of •OH. This study emphasized the essential role of BC in developing tailored hematite facets as a contaminant remediation substrate, and provided important insights into the design of efficient heterogeneous Fenton-like systems.
铁矿物暴露晶面的固有性质在矿物界面的非均相反应中起着关键作用,添加共催化剂已被阐明可以进一步增强污染物降解反应。在这里,揭示了不同赤铁矿优势暴露晶面({001}、{012}、{100}和{113})与纳米碳化硼(BC)的协同类芬顿催化反应活性。在 5 小时内,与 BC/HO 体系中的累积•OH(96.9 μM)相比,BC/HO 体系中•OH 的累积量减少了 19.6%,而{001}/BC/HO、{012}/BC/HO、{100}/BC/HO 和{113}/BC/HO 体系中的•OH 累积量分别增加了 53.8%、75.9%和 84.0%。值得注意的是,{113}/BC/HO 体系表现出降解广谱有机污染物的强大能力,包括典型的苯酚、内分泌干扰物(双酚 A)、抗生素(磺胺嘧啶)、染料(罗丹明 B 和亚甲蓝)和农药(莠去津)。在类芬顿反应中,{113}/BC/HO 体系表现出更高的协同因子、Fe(III)/Fe(II)循环速率和 Fe-O-B 键数量,优于其他体系,因此表现出良好的•OH 生成和污染物氧化催化性能。铁物种和 X 射线光电子能谱(XPS)分析表明,B-B 键和界面亚氧化硼(例如 B-O)可以提供电子,促进 Fe(III)还原,从而促进 Fe(III)/Fe(II)循环。密度泛函理论(DFT)结果表明,在赤铁矿{113}、{100}和{012}晶面上形成了 Fe-O-B 键,有利于断裂结合 HO 分子的 O-O 键,从而提高了•OH 的生成。本研究强调了 BC 在开发定制赤铁矿晶面作为污染物修复基质方面的重要作用,并为设计高效的非均相类芬顿体系提供了重要见解。