CO2环境下共热解制备纳米氧化铁金属生物炭及吸附Cr(VI)的研究

Jeong-Yun Jang, Sun Joon Kim
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引用次数: 0

摘要

本研究探讨了在CO 2环境下,将纳米氧化铁(NIO)与咖啡渣(CG)混合在热解过程中对合成气(h2和CO)的生成以及去除水溶液中Cr(VI)的生物炭性能的影响。CG和NIO物理混合;添加NIO时,CG质量保持在1g。根据质量比,将所得溶液命名为NICG1(NIO/CG比=1:1)。与CG单次热解650℃时的合成气产生量(h2 = 0.37 mol %, CO = 0.28 mol %)相比,添加nio基添加剂共热解使合成气产生量增加,在相同温度下,h2和CO的测量浓度分别达到0.99 mol %和0.86 mol %。在pH效应实验中,NICG1在pH = 2的酸性条件下的去除率最高。吸附动力学实验表明,拟二级速率模型适用于NICG1对Cr(VI)的去除。NICG1对Cr(VI)的去除符合Freundlich等温吸附模型(r2 = 0.9807)。综上所述,纳米氧化铁(III)与咖啡渣共热解可以被认为是同时产生合成气(h2和CO)作为燃料(能源)和金属生物炭作为吸附剂的有效资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Study on Preparation of Nano Iron Oxides-Based Metal Biochar Using Co-Pyrolysis in a CO2 Environment and Adsorption of Cr(VI)
This study explored the effects of blending nano iron (III) oxides (NIO) with coffee grounds (CG) in a pyrolytic process under a CO 2 environment on the generation of syngas (H 2 and CO) and biochar properties regarding the removal of Cr(VI) from aqueous solutions. CG and NIO were physically mixed; CG was mass maintained at 1 g while NIO was added. Based on the mass ratio, the resulting solution was named NICG1(NIO/CG ratio=1:1). Compared with the generation amounts of syngas (0.37 mole% H 2 & 0.28 mole% CO) at 650°C from single pyrolysis of CG, co-pyrolysis with NIO-based additives resulted in increased production of syngas, with the measured concentrations of H 2 and CO reaching 0.99 mole% and 0.86 mole% at the same temperature, respectively. During the pH effect experiments, NICG1 demonstrated the highest removal efficiency under acidic conditions with pH = 2. Adsorption kinetic experiments demonstrated that the pseudo-second-order rate model was suitable for assessing the removal of Cr(VI) by NICG1. Furthermore, the removal of Cr(VI) using NICG1 fitted well with the Freundlich isothernm adsorption model (R 2 = 0.9807). In conclusion, co-pyrolysis of blending nano iron(III) oxide and coffee grounds can be considered an efficient resource for simultaneously producing syngas (H 2 and CO) as a fuel (energy resource) and metal-biochar as an adsorbent.
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