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    姬国钊

    • 副教授     博士生导师   硕士生导师
    • 性别:男
    • 毕业院校:昆士兰大学
    • 学位:博士
    • 所在单位:环境学院
    • 办公地点:西部校区环境学院B713
    • 联系方式:0411-84706206
    • 电子邮箱:guozhaoji@dlut.edu.cn

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    Alkaline Thermal Treatment of Cellulosic Biomass for H-2 Production Using Ca-Based Bifunctional Materials

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    论文类型:期刊论文

    第一作者:Zhao, Ming

    通讯作者:Zhao, X (reprint author), Tsinghua Univ, Sch Environm, Beijing 100084, Peoples R China.; Zhao, X (reprint author), China Agr Univ, Coll Water Resources & Civil Engn, Beijing 100083, Peoples R China.

    合写作者:Cui, Xiaomin,Ji, Guozhao,Zhou, Hui,Vuppaladadiyam, Arun K.,Zhao, Xiao

    发表时间:2019-01-07

    发表刊物:ACS SUSTAINABLE CHEMISTRY & ENGINEERING

    收录刊物:SCIE

    卷号:7

    期号:1

    页面范围:1202-1209

    ISSN号:2168-0485

    关键字:Cellulosic biomass; Alkaline thermal treatment; Hydrogen production; Bifunctional materials

    摘要:Hydrogen production from cellulosic biomass not only provides a sustainable approach to cope with the growing demand for energy but also facilitates the relief of environmental burden. In this study, we developed a series of Ca-based bifunctional materials (Ca(OH)(2) and Ni composites) for alkaline thermal treatment (ATT) of cellulose to produce high purity hydrogen at moderate temperatures (350-450 degrees C). Ca(OH)(2) served predominantly as a CO2 carrier and a H2O donor, and enlarged the surface area of the materials to improve H-2 production. However, excess Ca(OH)(2) tended to cover Ni particles and block pore structures resulting in a suppressed H-2 production. Ni promoted tar cracking and enhanced H-2 production, but the surface area of catalyst decreased with an increment in Ni, which suppressed H-2 generation. The yield of hydrogen was improved at elevated temperature. The maximum hydrogen yield, 34.5 mmol.g(-1) with 77% volume fraction, was obtained by adopting a molar ratio of cellulose:Ca(OH)(2):Ni as 1:6:2 at 450 degrees C for 10 min. GC-MS analysis results of tar products revealed that Ca(OH)(2) promoted primary pyrolysis of cellulose, and Ni promoted the decomposition of furan ring derivatives. The reaction temperature affected the distribution rather than the composition of the tar products.