Bharath G, Rambabu K, Morajkar Pranay P, Jayaraman Raja, Theerthagiri Jayaraman, Lee Seung Jun, Choi Myong Yong, Banat Fawzi
Department of Chemical Engineering, Khalifa University, P.O. Box 127788, Abu Dhabi, United Arab Emirates.
Department of Chemical Engineering, Khalifa University, P.O. Box 127788, Abu Dhabi, United Arab Emirates.
J Hazard Mater. 2021 May 5;409:124980. doi: 10.1016/j.jhazmat.2020.124980. Epub 2020 Dec 25.
In recent years, substantial progress has been made towards developing effective catalysts for the hydrogenation of CO into fuels. However, the quest for a robust catalyst with high activity and stability still remains challenging. In this study, we present a cost-effective catalyst composed of MoS nanosheets and functionalized porous date seed-derived activated carbon (f-DSAC) for hydrogenation of CO into formic acid (FA). As-fabricated MoS/f-DSAC catalysts were characterized by FE-SEM, XRD, Raman, FT-IR, BET, and CO-TPD analyses. At first, bicarbonate (HCO) was successfully converted into FA with a high yield of 88% at 200 °C for 180 min under 10 bar H atmosphere. A possible reaction pathway for the conversion of HCO into FA is postulated. The catalyst has demonstrated high activity and long-term stability over five consecutive cycles. Additionally, MoS/f-DSAC catalyst was effectively used for the conversion of gaseous CO into FA at 200 °C under 20 bar (CO/H = 1:1) over 15 h. The catalyst exhibited a remarkable TOF of 510 h with very low activation energy of 12 kJ mol, thus enhancing the catalytic conversion rate of CO into FA. Thus, this work demonstrates the MoS/f-DSAC nanohybrid system as an efficient non-noble catalyst for converting CO into fuels.
近年来,在开发用于将CO氢化为燃料的有效催化剂方面取得了重大进展。然而,寻求一种具有高活性和稳定性的坚固催化剂仍然具有挑战性。在本研究中,我们提出了一种由MoS纳米片和功能化多孔枣籽衍生活性炭(f-DSAC)组成的经济高效催化剂,用于将CO氢化为甲酸(FA)。通过FE-SEM、XRD、拉曼、FT-IR、BET和CO-TPD分析对制备的MoS/f-DSAC催化剂进行了表征。首先,在10 bar H气氛下,于200°C反应180分钟,碳酸氢盐(HCO)成功转化为FA,产率高达88%。推测了HCO转化为FA的可能反应途径。该催化剂在连续五个循环中表现出高活性和长期稳定性。此外,MoS/f-DSAC催化剂在20 bar(CO/H = 1:1)下于200°C有效地用于气态CO转化为FA,反应时间超过15小时。该催化剂表现出510 h的显著TOF,活化能非常低,为12 kJ mol,从而提高了CO转化为FA的催化转化率。因此,这项工作证明了MoS/f-DSAC纳米杂化体系是一种将CO转化为燃料的高效非贵金属催化剂。