Fe/g-C3N4 催化剂表面改性对 CO 加氢产物分布的影响

Q3 Energy
Yu SUN, Xinhua GAO, Qingxiang MA, Subing FAN, Tiansheng ZHAO, Jianli ZHANG
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引用次数: 0

摘要

采用 H2O2/NH3-H2O 预处理尿素热缩合制备的氮化碳(g-C3N4),并以其为载体,通过浸渍法获得 Fe/g-C3N4 催化剂。研究了改性前后催化剂在 CO 加氢过程中的催化性能。结合 XRD、SEM、TEM、FT-IR、TG、CO2-TPD、CO-TPD、H2-TPR、接触角测量、N2 物理吸附和解吸等详细表征,研究了表面预处理对 Fe/g-C3N4 催化剂质构性质和 CO 加氢产物分布的影响。结果表明,各种预处理技术对催化剂的质构特性和催化性能有显著影响。制备的 g-C3N4 具有典型的蜂窝状结构,与高度分散的铁具有很强的相互作用。改性前后的材料都具有亲水性,而用 H2O2 和 NH3-H2O 处理后亲水性增强。用 H2O2 处理可增强表面羟基。NH3-H2O 处理可改善表面氨基,促进 CO 吸附,并促进 Fe(NCN)相的形成。所有预处理催化剂的表面碱性都得到了增强。两步修饰催化剂 Fe/AM-g-C3N4 的水气变换(WGS)反应活性较低,CO 加氢中 CO2 的选择性降低到 11.61%。由于 Fe/AM-g-C3N4 的碱性增强,烯烃的二次加氢能力受到抑制,从而获得了更高的烯烃选择性(C= 2-C= 4 为 32.37%,O/P 值为 3.23)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of surface modification of Fe/g-C3N4 catalyst on the product distribution in CO hydrogenation

Carbon nitride (g-C3N4) prepared using thermal condensation of urea was pretreated by H2O2/NH3·H2O and used as support to obtain Fe/g-C3N4 catalyst via impregnation method. The catalytic performance of the catalysts both before and after modification was investigated in CO hydrogenation. Combining detailed characterizations, such as XRD, SEM, TEM, FT-IR, TG, CO2-TPD, CO-TPD, H2-TPR, contact angle measurement, and N2 physical adsorption and desorption, we investigated the effects of surface pretreatment on the texture properties of Fe/g-C3N4 catalysts and the product distribution of CO hydrogenation. The results demonstrate that various pretreatment techniques have significant influences on the textural properties and catalytic performance of the catalysts. The prepared g-C3N4 with a typical honeycomb structure has strong interaction with highly dispersed Fe. Both before and after modification, the materials are hydrophilic, and the hydrophilicity is increased after treatment with H2O2 and NH3·H2O. Treatment with H2O2 enhances surface hydroxyl groups. NH3·H2O treatment improves surface amino groups, promotes CO adsorption, and facilitates the formation of Fe(NCN) phase. The surface basicity of all pretreated catalysts is enhanced. The water gas shift (WGS) reaction activity of the two-step modified catalyst Fe/AM-g-C3N4 was lower, and the CO2 selectivity in CO hydrogenation was reduced to 11.61%. Due to the enhanced basicity of Fe/AM-g-C3N4, the secondary hydrogenation ability of olefins was inhibited to obtain higher olefin selectivity with C= 2–C= 4 of 32.37% and an O/P value of 3.23.

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来源期刊
燃料化学学报
燃料化学学报 Chemical Engineering-Chemical Engineering (all)
CiteScore
2.80
自引率
0.00%
发文量
5825
期刊介绍: Journal of Fuel Chemistry and Technology (Ranliao Huaxue Xuebao) is a Chinese Academy of Sciences(CAS) journal started in 1956, sponsored by the Chinese Chemical Society and the Institute of Coal Chemistry, Chinese Academy of Sciences(CAS). The journal is published bimonthly by Science Press in China and widely distributed in about 20 countries. Journal of Fuel Chemistry and Technology publishes reports of both basic and applied research in the chemistry and chemical engineering of many energy sources, including that involved in the nature, processing and utilization of coal, petroleum, oil shale, natural gas, biomass and synfuels, as well as related subjects of increasing interest such as C1 chemistry, pollutions control and new catalytic materials. Types of publications include original research articles, short communications, research notes and reviews. Both domestic and international contributors are welcome. Manuscripts written in Chinese or English will be accepted. Additional English titles, abstracts and key words should be included in Chinese manuscripts. All manuscripts are subject to critical review by the editorial committee, which is composed of about 10 foreign and 50 Chinese experts in fuel science. Journal of Fuel Chemistry and Technology has been a source of primary research work in fuel chemistry as a Chinese core scientific periodical.
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