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改性聚苯乙烯纳米塑料在生物质衍生活性炭上的吸附:球磨活化研究

Adsorption of modified polystyrene nanoplastics on biomass-derived activated carbons: A study of ball mill activation.

作者信息

Sanz-Santos Eva, Álvarez-Montero Ariadna, Gómez-Avilés Almudena, Belver Carolina, Bedia Jorge

机构信息

Chemical Engineering Department, Universidad Autónoma de Madrid, Campus Cantoblanco, Madrid, 28049, Spain; Department of Chemical, Energetic and Mechanical Technology, Universidad Rey Juan Carlos, Móstoles, 28933, Spain.

Chemical Engineering Department, Universidad Autónoma de Madrid, Campus Cantoblanco, Madrid, 28049, Spain.

出版信息

J Environ Manage. 2025 Sep;391:126654. doi: 10.1016/j.jenvman.2025.126654. Epub 2025 Jul 19.

Abstract

This study focuses on synthesizing activated carbons using lignin and sawdust as precursors, with FeCl employed as an activating agent, aimed at adsorbing of modified polystyrene nanoparticles. The impact of ball milling during the impregnation process was evaluated, revealing that the best results were obtained with a milling time of 10 min. This method resulted in activated carbons with enhanced porosity compared to those synthesized without milling. However, extending the milling time adversely affected the performance, likely due to heat generated by friction in the ball mill, which caused excessive dehydration and impeded the proper carbonization process. The activated carbons demonstrating the best performance were L-10 (derived from lignin) with a BET surface area of 1258 m g, and S-10 (derived from sawdust) with 1072 m g. The materials exhibited high adsorption capacities of 70.08 and 65.77 mg g for polystyrene nanoparticles (PSNPs) with L-10 and S-10 carbons, respectively. These results align with the higher surface areas of the adsorbent materials, emphasizing the crucial role of porosity in adsorption efficiency. Notably, the pore sizes of the activated carbons were smaller than the diameter of the PSNPs, minimizing diffusion effects and concentrating adsorption activity on the external surfaces. In addition, the adsorption process was governed by electrostatic interactions, with additional contributions from π-π interactions between the aromatic structures of the activated carbon and the benzene rings of the polystyrene. When examining polystyrene nanoparticles modified with amino and carboxyl groups, L-10 and S-10 exhibited higher affinity for amine-functionalized polystyrene while showing repulsion toward carboxyl-functionalized polystyrene.

摘要

本研究聚焦于以木质素和锯末为前驱体、以氯化铁为活化剂合成活性炭,旨在吸附改性聚苯乙烯纳米颗粒。评估了浸渍过程中球磨的影响,结果表明,球磨10分钟可获得最佳效果。与未进行球磨合成的活性炭相比,该方法得到的活性炭孔隙率更高。然而,延长球磨时间会对性能产生不利影响,这可能是由于球磨过程中摩擦产生的热量导致过度脱水,阻碍了正常的碳化过程。表现最佳的活性炭是L-10(源自木质素),其BET表面积为1258 m²/g,以及S-10(源自锯末),其BET表面积为1072 m²/g。对于聚苯乙烯纳米颗粒(PSNPs),L-10和S-10活性炭的吸附容量分别高达70.08和65.77 mg/g。这些结果与吸附剂材料较高的表面积相符,强调了孔隙率在吸附效率中的关键作用。值得注意的是,活性炭的孔径小于PSNPs的直径,从而将扩散效应降至最低,并使吸附活性集中在外表面。此外,吸附过程受静电相互作用控制,活性炭的芳香结构与聚苯乙烯的苯环之间的π-π相互作用也起到了额外作用。在研究用氨基和羧基修饰的聚苯乙烯纳米颗粒时,L-10和S-10对胺功能化聚苯乙烯表现出更高的亲和力,而对羧基功能化聚苯乙烯表现出排斥作用。

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