Removal of triclosan and bisphenol A from water by selected natural adsorbents

化学 双酚A 吸附 三氯生 吸附 化学工程 环境化学 活性炭 膨润土 壬基酚 水处理 动力学 色谱法 斜发沸石 2,4-二氯苯酚 双酚 流出物 疏水效应 比表面积 选择性 有机粘土 生物累积 地表水 粉末活性炭处理 三氯卡班 药品和个人护理产品的环境影响 有机化学
作者
H. Lubarsky,T.O. Olanrewaju,S. Shepherd,D.M. Wilkins,D.H. Phillips
出处
期刊:Separation and Purification Technology [Elsevier BV]
卷期号:394: 137281-137281
标识
DOI:10.1016/j.seppur.2026.137281
摘要

Endocrine-disrupting compounds (EDCs) like triclosan (TCS) and bisphenol A (BPA) are persistent micropollutants in aquatic environments that threaten human health and ecosystems through bioaccumulation and disruption of hormonal pathways. Conventional water treatment processes often fail to achieve sufficient removal of these compounds, necessitating the development of efficient adsorptive methods. Rather than introducing new materials , this study compares the adsorption capabilities of four types of commercially relevant natural adsorbents—granular activated carbon (GAC), granular ferric hydroxide (GFH), natural clinoptilolite zeolite, and surfactant-modified bentonite organoclay—chosen for their structural diversity and environmental relevance. All experiments were conducted under identical batch conditions using single-solute systems to enable direct comparison of adsorption behaviour. Batch experiments and characterisation analysis assessed physical properties, sorption efficiency, kinetics, and equilibrium behaviour for TCS and BPA removal. Results revealed that GAC exhibited the most consistent and broad-spectrum removal (>95% for both TCS and BPA), suggesting that adsorption is governed by chemisorption, π–π interactions, and hydrogen bonding, best described by pseudo-second-order kinetics and suitable equilibrium models. Organoclays achieved near-complete TCS removal (up to 99.6%) via surfactant-mediated hydrophobic partitioning but were less effective for BPA (48–67%). GFH displayed remarkable selectivity, removing TCS with >90% efficiency but showing negligible affinity for BPA, reflecting compound-specific surface interactions such as surface complexation rather than non-specific adsorption . Zeolites demonstrated limited capacity, achieving ≤25% TCS removal and no detectable BPA adsorption, constrained by pore size and surface charge. These findings establish compound-specific adsorption mechanisms and selectivity patterns and highlight GAC as the most effective broad-spectrum option, while GFH and organoclays offer selective and potentially cost-effective alternatives. By decoupling surface area, pore structure, surface chemistry, and surface charge under controlled conditions, this study provides a mechanism-oriented comparative framework for adsorbent selection and optimisation in water treatment applications targeting EDCs.
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