SUN Yu, GAO Xinhua, MA Qingxiang, FAN Subing, ZHAO Tiansheng, ZHANG Jianli. Effect of surface modification of Fe/g-C3N4 catalyst on the product distribution in CO hydrogenation[J]. Journal of Fuel Chemistry and Technology, 2024, 52(1): 19-28. DOI: 10.1016/S1872-5813(23)60378-0
Citation: SUN Yu, GAO Xinhua, MA Qingxiang, FAN Subing, ZHAO Tiansheng, ZHANG Jianli. Effect of surface modification of Fe/g-C3N4 catalyst on the product distribution in CO hydrogenation[J]. Journal of Fuel Chemistry and Technology, 2024, 52(1): 19-28. DOI: 10.1016/S1872-5813(23)60378-0

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 \rmC_2^=-\rmC_4^=\;s \;\rmof 32.37% and an O/P value of 3.23.
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