利用蜂窝状掺氮碳纳米片快速去除全氟辛酸(PFOA):竞争污染物/水基质选择性吸附全氟辛酸的机理

IF 7.4 Q1 ENGINEERING, ENVIRONMENTAL
Lingyu Chen, Kuanchang He, Wei Li, Dongmei Ma, Xiaodong Xin, Gang Wang, Qian Liu, Lihui Yang, Faliang Cheng, Sihao Lv, Defeng Xing
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引用次数: 0

摘要

最近,碳基吸附剂被认为是高效去除全氟辛酸(PFOA)的先进材料;然而,人们对全氟辛酸在竞争污染物/水基质中的选择性吸附仍缺乏基本的了解。本文报告了一种新型蜂窝状掺氮碳纳米片(HL-NC@Ni-800)材料,用于快速吸附 PFOA。PFOA 的选择性吸附归因于:(i) 有利的立体阻碍作用使 PFOA 被快速稳定地吸附;(ii) 蜂窝状介孔结构提供了丰富的吸附位点;(iii) PFOA 阴离子与镍阳离子之间的静电吸引作用;(iv) PFOA 尾部与氮功能基团之间的疏水效应;(v) 路易斯酸碱效应。因此,PFOA 从竞争污染物(如 1,4-二恶烷和磺胺甲噁唑)中的去除率分别为 94.6% 和 89.6%,从水基质(如无机阴离子)中的去除率为 ∼84-94% ,从真正的高盐度海水中的去除率为 75.6-78.4% 。计算得出的 HL-NC@Ni-800 对 PFOA 的最大吸附容量(qm)飙升至 184.89 mg-g-1。此外,不同立体构象的 PFOA 在 HL-NC@Ni-800 上的热力学吸附为其对 PFOA 的高效吸附性能提供了理论解释。这项研究为全氟辛酸高效吸附剂的合成方法提供了一种新的策略,同时也阐明了全氟辛酸对竞争污染物/水基质选择性吸附的机理,为设计更高效的吸附剂处理全氟辛酸污染水提供了指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fast Perfluorooctanoic Acid (PFOA) Removal with Honeycomb-like Nitrogen-Doped Carbon Nanosheets: Mechanisms for the Selective Adsorption of PFOA over Competing Contaminants/Water Matrix

Fast Perfluorooctanoic Acid (PFOA) Removal with Honeycomb-like Nitrogen-Doped Carbon Nanosheets: Mechanisms for the Selective Adsorption of PFOA over Competing Contaminants/Water Matrix
Carbon-based adsorbents have been recently identified as advanced materials for the efficient removal of perfluorooctanoic acid (PFOA); however, the fundamental understanding of the selective adsorption of PFOA over competing contaminants/water matrix is still lacking. Herein, a novel honeycomb-like nitrogen-doped carbon nanosheet (HL-NC@Ni-800) material was reported for the rapid adsorption of PFOA. The PFOA selective adsorption was attributed to (i) favorable steric hindrance that allowed rapid and stable PFOA adsorption, (ii) abundant adsorption sites provided by the honeycomb-like mesoporous structure, (iii) electrostatic attraction between the PFOA anion and nickel cation, (iv) hydrophobic effect between the PFOA tail and nitrogen functional groups, and (v) Lewis acid–base effect. Consequently, PFOA was efficiently removed from the competing contaminants such as 1,4-dioxane and sulfamethoxazole by 94.6 and 89.6%, respectively, as well as the water matrix such as inorganic anions by ∼84–94% and real high-salinity seawater by 75.6–78.4%. The calculated maximum adsorption capacities (qm) of HL-NC@Ni-800 for PFOA soared to 184.89 mg·g–1. In addition, the thermodynamically favorable adsorption of PFOA with different steric conformations on HL-NC@Ni-800 provided theoretical explanations for its high-efficiency adsorption performance toward PFOA. This study provides a novel strategy for the synthesis method of efficient adsorbents for PFOA and also elucidates the mechanistic understandings of PFOA selective adsorption over competing contaminants/water matrix, for guiding the design of more efficient adsorbents to treat PFOA-contaminated water.
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来源期刊
ACS ES&T engineering
ACS ES&T engineering ENGINEERING, ENVIRONMENTAL-
CiteScore
8.50
自引率
0.00%
发文量
0
期刊介绍: ACS ES&T Engineering publishes impactful research and review articles across all realms of environmental technology and engineering, employing a rigorous peer-review process. As a specialized journal, it aims to provide an international platform for research and innovation, inviting contributions on materials technologies, processes, data analytics, and engineering systems that can effectively manage, protect, and remediate air, water, and soil quality, as well as treat wastes and recover resources. The journal encourages research that supports informed decision-making within complex engineered systems and is grounded in mechanistic science and analytics, describing intricate environmental engineering systems. It considers papers presenting novel advancements, spanning from laboratory discovery to field-based application. However, case or demonstration studies lacking significant scientific advancements and technological innovations are not within its scope. Contributions containing experimental and/or theoretical methods, rooted in engineering principles and integrated with knowledge from other disciplines, are welcomed.
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