Cu-MOF-derived Cu nanoparticles decorated porous N-doped biochar for low-temperature H2S desulfurization

烟气脱硫 生物炭 热解 吸附 硫黄 硫化氢 化学工程 多孔性 材料科学 纳米颗粒 核化学 无机化学 化学 冶金 纳米技术 有机化学 复合材料 工程类
作者
Lingwen Song,Yi Yuan,Yuan Wang,Tian C. Zhang,Ge He,Shaojun Yuan
出处
期刊:Fuel [Elsevier]
卷期号:368: 131682-131682 被引量:3
标识
DOI:10.1016/j.fuel.2024.131682
摘要

Hydrogen sulfide (H2S) is a highly toxic and corrosive gas that poses significant risks to human health and the environment. Therefore, the development of an adsorbent capable of efficiently purifying H2S at room temperature remains a challenging task. In this study, a novel composite adsorbent with a specific surface area of 434 m2·g−1 was fabricated by modifying porous N-doped biochar with Cu nanoparticles (Cu/NBC) derived from Cu-MOFs for low-temperature desulfurization of H2S. The effect of pyrolysis temperature and the doping ratio of Cu-MOFs to biochar on the desulfurization performance of H2S for the as-prepared Cu/NBC was comprehensively investigated. Experimental results indicated that the desulfurization capability of the optimized Cu/NBC-600-1 adsorbent (synthesized at a pyrolysis temperature of 600 °C and a doping ratio of 1:1) was significantly affected by the desulfurization conditions, and the optimal conditions were determined to be at 25 °C, with 20 % oxygen content and 70 % relative humidity. Under the optimized conditions, the Cu/NBC-600-1 adsorbent exhibited a high H2S removal capacity of 158.28 mg·g−1, which was about 3.8 times higher than that of the pristine N-doped biochar. The desulfurization mechanism of the Cu/NBC composite was demonstrated to involve reactive adsorption and catalytic oxidation, resulting in the formation of elemental sulfur and copper sulfides as the main products. This study not only provides a promising approach to modify porous biochar with MOF derivatives, but also offers an effective strategy to remove low concentration H2S at room temperature.
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