Sorption of carbamazepine by commercial graphene oxides: A comparative study with granular activated carbon and multiwalled carbon nanotubes

被引:107
作者
Cai, Nan [1 ]
Larese-Casanova, Philip [1 ]
机构
[1] Northeastern Univ, Dept Civil & Environm Engn, Boston, MA 02115 USA
基金
美国国家科学基金会;
关键词
Graphene; Carbamazepine; Endocrine disrupting compounds; Sorption processes; Freundlich isotherm; Water treatment; MOLECULARLY IMPRINTED POLYMERS; ENDOCRINE DISRUPTING COMPOUND; DRINKING-WATER TREATMENT; AQUEOUS-SOLUTION; WASTE-WATER; ADSORPTION CHARACTERISTICS; PIMEPHALES-PROMELAS; ORGANIC-CHEMICALS; CATIONIC DYES; BISPHENOL-A;
D O I
10.1016/j.jcis.2014.03.038
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hypothesis: Graphene nanosheet materials represent a potentially new high surface area sorbent for the treatment of endocrine disrupting compounds (EDCs) in water. However, sorption behavior has been reported only for laboratory graphene prepared by a laborious and hazardous graphite exfoliation process. A careful examination of commercially available, clean, high-volume produced graphene materials should reveal whether they are appropriate for sorbent technologies and which physicochemical properties most influence sorption performance. Experiments: In this study, three commercially available graphene oxide powders of various particle sizes, specific surface areas, and surface chemistries were evaluated for their sorption performance using carbamazepine and nine other EDCs and were compared to that of conventional granular activated carbon (GAC) and multi-walled carbon nanotubes (MWCNTs). Findings: Sorption kinetics of carbamazepine on graphene oxide powders was rapid and reversible with alcohol washing, consistent with pi-pi interactions. The various sorption extents as described by Freundlich isotherms were best explained by available surface area, and only the highest surface area graphene oxide (771 m(2)/g) out-performed GAC and MWCNTs. Increasing pH caused more negative surface charge, a twofold decrease in sorption of anionic ibuprofen, a onefold increase in sorption of cationic atenolol, and no change for neutral carbamazepine, highlighting the role of electrostatic interactions. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:152 / 161
页数:10
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