Functionalized graphene oxide for Cr (VI) removal: A systematic review of functional groups, mechanisms, and environmental implications

IF 7.9 Q1 ENGINEERING, MULTIDISCIPLINARY
Somayeh Rahdar , Aliakbar Dehghan , Mojtaba Davoudi , Mahmoud Shams
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引用次数: 0

Abstract

Hexavalent chromium Cr (VI) pollution poses significant health and environmental risks, prompting the exploration of graphene oxide (GO)-based adsorbents as a promising removal solution due to their unique properties. This systematic review (2014–2023) examines hexavalent chromium (Cr (VI)) removal using functionalized GO, focusing on the role of surface groups such as amine (-NH₂), carboxyl (-COOH), thiol (-SH), sulfonic (-SO₃H), and metal oxides in enhancing adsorption. Among 53 studies, amine-functionalized GO demonstrated superior efficiency owing to its protonation in acidic conditions, nitrogen's lone electron pair, increased positive surface charge, and expanded interlayer spacing. Carboxyl/hydroxyl groups facilitated ion exchange and Cr (VI)-to-Cr (III) reduction but showed weaker binding tendency. Sulfur-containing groups enabled physical adsorption via complexation but suffers lack of stability in acidic media. Despite limited direct Cr (VI) adsorption, metal oxides enhanced GO’s magnetic properties and stability. Reports indicated the pseudo-second-order model frequently described the adsorption processes, suggesting chemisorption is the rate-limiting step. Besides, depending on the functional groups and operating conditions, thermodynamic analysis revealed that Cr (VI) adsorption could occurs spontaneous, endothermic, or exothermic. Basically, a variety of the key operational parameters i.e. pH, initial concentration, contact time, and temperature, were evaluated for Cr (VI) adsorption on graphene-based adsorbents. The maximum removal efficiencies predominantly occurred in strong acidic condition i.e. pH 2–3, where protonation of functional groups develops strong electrostatic attraction to HCrO₄⁻. Tailoring carbon-based materials through rational functionalization and extending their working pH range toward neutrality warrants further attention in future studies. Within this context, emerging utilities such as machine learning and artificial intelligence offer a promising avenue to fulfill these goals.
功能化氧化石墨烯去除Cr (VI):对官能团、机制和环境影响的系统综述
六价铬铬(VI)污染带来了重大的健康和环境风险,氧化石墨烯(GO)吸附剂由于其独特的性能,促使人们探索其作为一种有前途的去除方案。这篇系统综述(2014-2023)研究了使用功能化氧化石墨烯去除六价铬(Cr (VI)),重点研究了表面基团如胺(-NH₂)、羧基(-COOH)、硫醇(-SH)、磺酸(-SO₃H)和金属氧化物在增强吸附中的作用。在53项研究中,胺官能化氧化石墨烯由于其在酸性条件下的质子化、氮的孤电子对、表面正电荷的增加和层间间距的扩大而表现出优异的效率。羧基/羟基促进离子交换和Cr (VI)到Cr (III)的还原,但结合倾向较弱。含硫基团可以通过络合作用进行物理吸附,但在酸性介质中缺乏稳定性。尽管对Cr (VI)的直接吸附有限,但金属氧化物增强了氧化石墨烯的磁性和稳定性。报告表明,伪二阶模型经常描述吸附过程,表明化学吸附是限速步骤。此外,根据官能团和操作条件的不同,热力学分析表明Cr (VI)的吸附可以自发、吸热或放热进行。基本上,各种关键操作参数,即pH,初始浓度,接触时间和温度,评估了Cr (VI)在石墨烯基吸附剂上的吸附。最大的去除效率主要发生在强酸性条件下,即pH 2-3,官能团的质子化对HCrO₄产生强烈的静电吸引力。通过合理功能化定制碳基材料,并将其工作pH范围向中性扩展,值得在未来的研究中进一步关注。在这种背景下,机器学习和人工智能等新兴实用程序为实现这些目标提供了一个有希望的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Results in Engineering
Results in Engineering Engineering-Engineering (all)
CiteScore
5.80
自引率
34.00%
发文量
441
审稿时长
47 days
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