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多氯二苯并对二恶英/呋喃在氮掺杂生物炭上吸附增强的密度泛函理论研究。

PCDD/F adsorption enhancement over nitrogen-doped biochar: A DFT-D study.

机构信息

State Key Laboratory of Clean Energy Utilization, Zhejiang University, Hangzhou, 310027, PR China.

State Key Laboratory of Clean Energy Utilization, Zhejiang University, Hangzhou, 310027, PR China.

出版信息

J Environ Manage. 2023 Oct 15;344:118611. doi: 10.1016/j.jenvman.2023.118611. Epub 2023 Jul 13.

Abstract

Polychlorinated dibenzo-p-dioxin/furans (PCDD/F) have a great threat to the environment and human health, resulting in controlling PCDD/F emissions to regulation far important for emission source. Considering 2,3,4,7,8-pentachlorodibenzo-p-furan (PeCDF) identified as the most contributor to international toxic equivalent, 2,3,4,7,8-PeCDF can be considered as the target molecule for the adsorption of PCDD/F emission from industries. With the aim to in-depth elucidate how different types of nitrogen (N) species enhance 2,3,4,7,8-PeCDF on the biochar and guide the specific carbon materials design for industries, systematic computational investigations by density functional theory calculations were conducted. The results indicate pristine biochar intrinsically interacts with 2,3,4,7,8-PeCDF by π-π electron donor and acceptor (EDA) interaction, six-membered carbon rings of PeCDF parallel to the biochar surface as the strongest adsorption configuration. Moreover, by comparison of adsorption energy (-150.16 kJ mol) and interaction distance (3.593 Å) of pristine biochar, environment friendly N doping can enhance the adsorption of 2,3,4,7,8-PeCDF on biochar. Compared with graphitic N doping and pyridinic N doping, pyrrolic N doping biochar presents the strongest interaction toward 2,3,4,7,8-PeCDF molecule due to the highest adsorption energy (-155.56 kJ mol) and shortest interaction distance (3.532 Å). Specially, the enhancing adsorption of PeCDF over N doped biochar attributes to the enhancing π-π electron EDA interaction and electrostatic interaction. In addition, the effect of N doping species on PeCDF adsorbed on the biochar is more than that of N doping content. Specially, the adsorption capacity of N doping biochar for PCDD/F can be improved by adding pyrrolic N group most efficiently. Furthermore, pyrrolic N and pyridinic N doping result in the entropy increase, and electrons transform from pyrrolic N and pyridinic N doped biochar to 2,3,4,7,8-PeCDF molecule. A complete understanding of the research would supply crucial information for applying N-doped biochar to effectively remove PCDD/F for industries.

摘要

多氯二苯并对二恶英/呋喃(PCDD/F)对环境和人类健康构成巨大威胁,因此控制 PCDD/F 排放以达到法规要求对于排放源来说至关重要。鉴于 2,3,4,7,8-五氯二苯并对二恶英(PeCDF)被确定为国际毒性当量的最主要贡献者,2,3,4,7,8-PeCDF 可以被视为从工业中吸附 PCDD/F 排放的目标分子。为了深入阐明不同类型的氮(N)物种如何增强生物炭对 2,3,4,7,8-PeCDF 的吸附,并指导针对工业的特定碳材料设计,通过密度泛函理论计算进行了系统的计算研究。结果表明,原始生物炭通过π-π电子供体和受体(EDA)相互作用与 2,3,4,7,8-PeCDF 发生内在相互作用,PeCDF 的六元碳环与生物炭表面平行是最强的吸附构型。此外,通过比较原始生物炭的吸附能(-150.16 kJ/mol)和相互作用距离(3.593 Å),环境友好的 N 掺杂可以增强 2,3,4,7,8-PeCDF 在生物炭上的吸附。与石墨 N 掺杂和吡啶 N 掺杂相比,吡咯 N 掺杂生物炭对 2,3,4,7,8-PeCDF 分子表现出最强的相互作用,因为其吸附能最高(-155.56 kJ/mol),相互作用距离最短(3.532 Å)。特别地,N 掺杂生物炭对 PeCDF 的增强吸附归因于增强的π-π电子 EDA 相互作用和静电相互作用。此外,N 掺杂物种对吸附在生物炭上的 PeCDF 的影响大于 N 掺杂含量的影响。特别地,通过最有效地添加吡咯 N 基团,可以提高 N 掺杂生物炭对 PCDD/F 的吸附容量。此外,吡咯 N 和吡啶 N 的掺杂导致熵增加,电子从吡咯 N 和吡啶 N 掺杂的生物炭转移到 2,3,4,7,8-PeCDF 分子。对这项研究的全面了解将为应用 N 掺杂生物炭有效去除工业 PCDD/F 提供关键信息。

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