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萘和菲在核桃壳基活性炭上的竞争吸附及理论计算验证

Competitive adsorption of naphthalene and phenanthrene on walnut shell based activated carbon and the verification theoretical calculation.

作者信息

Wu Zhansheng, Sun Zhonghai, Liu Pengyun, Li Qing, Yang Renpeng, Yang Xia

机构信息

School of Environmental and Chemical Engineering, Xi'an Polytechnic University Xi'an 710048 P. R. China

School of Chemistry and Chemical Engineering, Shihezi University Shihezi 832003 China.

出版信息

RSC Adv. 2020 Mar 13;10(18):10703-10714. doi: 10.1039/c9ra09447d. eCollection 2020 Mar 11.

Abstract

Walnut shell based activated carbon (WAC) was prepared microwave-assisted KOH activation. The adsorption behaviors towards naphthalene (NAP) and phenanthrene (PHE) over WAC were studied, both in single- and binary-compound systems. Characterization results reveal the excellent microporous structure of WAC, with a micropore specific surface area of 438.5 m g. The functional groups of walnut shell precursor surface were activated through microwave irradiation. In both systems, the pseudo-second-order model can better describe the adsorption kinetic data of PAHs over WAC at all experimental conditions. Mass transfer mechanism analysis shows that film diffusion was the rate-limiting step during the adsorption process. The adsorption amount of PAHs on WAC decreased as pH values increased, and the equilibrium data can be fitted by the Freundlich isotherm model well. In binary-component systems, the presence of PHE prominently restrained the adsorption towards NAP, and the Sheindorf-Rebhun-Sheintuch (SRS) model can fully fit the adsorption equilibrium experimental values of PAHs over WAC. In addition, the preferential adsorption behavior of PHE over WAC also was confirmed by theoretical calculations. The π-π complex between the active sites on the WAC surface and π-electrons of benzene rings from PAHs may play a major role in competitive adsorption. These results indicated that WAC was a potentially low-cost adsorbent for PAH elimination.

摘要

采用微波辅助氢氧化钾活化法制备了核桃壳基活性炭(WAC)。研究了WAC在单组分和双组分体系中对萘(NAP)和菲(PHE)的吸附行为。表征结果显示WAC具有优异的微孔结构,微孔比表面积为438.5 m²/g。核桃壳前驱体表面的官能团通过微波辐射得以活化。在两个体系中,准二级模型均能更好地描述所有实验条件下多环芳烃在WAC上的吸附动力学数据。传质机理分析表明,膜扩散是吸附过程中的限速步骤。多环芳烃在WAC上的吸附量随pH值升高而降低,平衡数据能很好地用Freundlich等温线模型拟合。在双组分体系中,菲的存在显著抑制了对萘的吸附,Sheindorf-Rebhun-Sheintuch(SRS)模型能完全拟合多环芳烃在WAC上的吸附平衡实验值。此外,理论计算也证实了菲在WAC上的优先吸附行为。WAC表面活性位点与多环芳烃苯环π电子之间的π-π络合作用可能在竞争吸附中起主要作用。这些结果表明WAC是一种潜在的低成本多环芳烃去除吸附剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d50/9050373/75fdc4303448/c9ra09447d-f1.jpg

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