Gao Yu, Liu Ying, Zhao Xu, Liu Xinchao, Sun Qina, Jiao Tifeng
State Key Laboratory of Metastable Materials Science and Technology, Hebei Key Laboratory of Heavy Metal Deep-Remediation in Water and Resource Reuse, School of Environmental and Chemical Engineering, Yanshan University, Qinhuangdao 066004, China.
Molecules. 2025 Apr 13;30(8):1743. doi: 10.3390/molecules30081743.
Chromium-containing wastewater poses severe threats to ecosystems and human health due to the high toxicity of hexavalent chromium (Cr(VI)). Although iron oxide nanoparticles (IONPs) show promise for Cr(VI) removal, their practical application is hindered by challenges in recovery and reuse. Herein, a novel three-dimensional porous nanocomposite, cyst shell biochar-supported iron oxide nanoparticles (ACSC@ IONP), was synthesized via synchronous pyrolysis of Fe-impregnated cyst shells (ACSs) and in situ reduction of iron. The optimized composite C@Fe-3, prepared with 1 mol/L Fe and pyrolyzed at 450 °C for 5 h, exhibited rapid removal equilibrium within 5-10 min for both Cr(VI) and total chromium (Cr(total)), attributed to synergistic reduction of Cr(VI) to Cr(III) and adsorption of Cr(VI) and Cr(III). The maximum Cr(total) adsorption capacity was 110.1 mg/g at pH 2, as determined by the Sips isothermal model for heterogeneous adsorption. Competitive experiments demonstrated robust selectivity for Cr(VI) removal even under a 64-fold excess of competing anions, with an interference order of SO > NO > Cl. Remarkably, C@Fe-3 retained 65% Cr(VI) removal efficiency after four adsorption-desorption cycles. This study provides a scalable and eco-friendly strategy for fabricating reusable adsorbents with dual functionality for chromium remediation.
含铬废水因六价铬(Cr(VI))的高毒性而对生态系统和人类健康构成严重威胁。尽管氧化铁纳米颗粒(IONPs)在去除Cr(VI)方面显示出潜力,但其实际应用受到回收和再利用方面挑战的阻碍。在此,通过对负载铁的囊壳(ACSs)进行同步热解和铁的原位还原,合成了一种新型三维多孔纳米复合材料——囊壳生物炭负载氧化铁纳米颗粒(ACSC@IONP)。用1 mol/L铁制备并在450℃热解5小时得到的优化复合材料C@Fe-3,对Cr(VI)和总铬(Cr(total))在5 - 10分钟内表现出快速的去除平衡,这归因于Cr(VI)协同还原为Cr(III)以及对Cr(VI)和Cr(III)的吸附。根据用于非均相吸附的Sips等温模型测定,在pH 2时最大Cr(total)吸附容量为110.1 mg/g。竞争实验表明,即使在竞争阴离子过量64倍的情况下,对Cr(VI)的去除仍具有强大的选择性,干扰顺序为SO > NO > Cl。值得注意的是,C@Fe-3在四个吸附 - 解吸循环后仍保留65%的Cr(VI)去除效率。本研究提供了一种可扩展且环保的策略,用于制备具有双重功能的可重复使用吸附剂以修复铬污染。