基于 Cr-M(M = Zr、La、Fe)的沸石催化剂将丙烷氧化脱氢为烯烃的 CO2 氧化反应

Catalysts Pub Date : 2024-06-07 DOI:10.3390/catal14060370
Mingqiao Xing, Ning Liu, Chengna Dai, Biaohua Chen
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引用次数: 0

摘要

二氧化碳氧化脱氢丙烷(CO2-ODHP)不仅有利于烯烃的生产,还有利于二氧化碳的排放控制,因此近年来备受关注。本文通过浸渍法制备了一系列单金属(Cr)和双金属(Zr、La、Fe)改性 ZSM-5 沸石。研究发现,双金属改性 ZSM-5 的 C3H8 和 CO2 转化率远高于单金属改性 Cr3%-ZSM-5 (Cr3%-Z5),尤其是 Cr3%Zr2%-ZSM-5 (Cr3%Zr2%-Z5)的活性(65.4%)和烯烃产率(1.65 × 103 μmol-gcat-1 h-1)最高。研究人员进行了各种表征,包括 XRD、N2 吸附-解吸、H2-TPR、拉曼、XPS、HAAD-STEM 和 TEM。结果表明,Zr 不仅有利于提高 Cr 的氧化还原能力,还有助于负载 Cr 物种的表面分散,这两点是 Cr3%Zr2%-Z5 具有优异活性的主要原因。为进一步提高 CO2-ODHP 催化性能,制备了一系列不同(ZSM-5/SBA-15)质量比的 Cr3%-ZSM-5@SBA-15-n 复合沸石催化剂(Cr3%-ZS-n,n = 0.5、2、6、16),筛选出最佳质量比为 6。在此基础上,进一步制备了 Cr3%Zr2%-ZS-6 化合物,并最终获得了更高的 CO2-ODHP 活性(76.9%)和烯烃产率(1.72 × 103 μmol-gcat-1 h-1)。最后,利用原位傅立叶变换红外光谱进一步研究了 CO2-ODHP 的反应机理,发现该反应遵循 Mars-van Krevelen 机理,即 CO2 通过生成多齿碳酸盐参与反应。Cr6+ 构成活性位点,在二氢反应后被还原成 Cr3+,然后被 CO2 进一步氧化成 Cr6+,形成多齿碳酸盐,从而使活性物种 Cr6+ 循环。此外,在布氏酸位点(有利于 C-C 键断裂)的辅助下,还产生了 C2H4 和 CH4。
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CO2 Oxidative Dehydrogenation of Propane to Olefin over Cr-M (M = Zr, La, Fe) Based Zeolite Catalyst
CO2 oxidative dehydrogenation of propane (CO2-ODHP), being not only favorable for olefin production but also beneficial for CO2 emission control, has recently attracted great attention. Here, a series of single metal (Cr) and bimetal (Zr, La, Fe) modified ZSM-5 zeolites were prepared via an impregnation method. It was found that the bimetal modified ZSM-5 possessed much higher C3H8 and CO2 conversion than that of monometallic modified Cr3%-ZSM-5 (Cr3%-Z5), especially for Cr3%Zr2%-ZSM-5 (Cr3%Zr2%-Z5), which displayed the highest activity (65.4%) and olefin yield (1.65 × 103 μmol·gcat−1 h−1). Various characterizations were performed, including XRD, N2 adsorption-desorption, H2-TPR, Raman, XPS, HAAD-STEM, and TEM. It was revealed that Zr not only favored an improvement in the redox ability of Cr, but also contributed to the surface dispersion of loaded Cr species, constituting two major reasons explaining the superior activity of Cr3%Zr2%-Z5. To further improve CO2-ODHP catalytic behavior, a series of Cr3%-ZSM-5@SBA-15-n composite zeolite catalysts with diverse (ZSM-5/SBA-15) mass ratios were prepared (Cr3%-ZS-n, n = 0.5, 2, 6, 16), which screened out an optimum mass ratio of six. Based on this, the Cr3%Zr2%-ZS-6 compound was further prepared, and it eventually achieved even higher CO2-ODHP activity (76.9%) and olefin yield (1.72 × 103 μmol·gcat−1 h−1). Finally, the CO2-ODHP reaction mechanism was further investigated using in situ FTIR, and it was found that the reaction followed the Mars–van Krevelen mechanism, wherein CO2 participated in the reaction through generation of polydentate carbonates. The Cr6+ constituted as the active site, which was reduced to Cr3+ after the dihydrogen reaction, and was then further oxidized into Cr6+ by CO2, forming polydentate carbonates, and thus cycling the reactive species Cr6+. Additionally, assisted by a Brönsted acid site (favoring breaking of the C-C bond), C2H4 and CH4 were produced.
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