Federal Research Center Boreskov Institute of Catalysis, Akad. Lavrentieva Ave. 5, Novosibirsk 630090, Russia.
Novosibirsk State University, Pirogova Str. 2, Novosibirsk 630090, Russia.
Dalton Trans. 2023 Jun 27;52(25):8756-8769. doi: 10.1039/d3dt00830d.
The mesoporous MgAlO support is promising for the design of efficient and stable to coking catalysts for natural gas and biofuel reforming into syngas. This work aims at doping this support with transition metal cations (Fe, Cr, Ti) to prevent the incorporation of Ni and rare-earth cations (Pr, Ce, Zr), loaded by impregnation, into its lattice along with providing additional sites for CO activation required to prevent coking. Doped MgAlMeO (Me = Fe, Ti, Cr) mesoporous supports prepared by the one-pot evaporation-induced self-assembly method with Pluronic P123 triblock copolymers were single-phase spinels. Their specific surface area varies in the range of 115-200 m g, decreasing to 90-110 m g after successive addition of the supporting nanocomposite active component 10 wt% PrCeZrO + (5 wt% Ni + 1% Ru) by impregnation. Mössbauer spectroscopy for iron-doped spinels confirmed the spatially uniform distribution of Fe cations in the lattice without clustering being mainly located at the octahedral positions. Fourier-transform infrared spectroscopy of the adsorbed CO molecules was performed to estimate the surface density of metal sites. In methane dry reforming, the positive effect of MgAlO support doping was observed from both a higher turn-over frequency as compared with the catalyst on the undoped support as well as the highest efficient first-order rate constant for the Cr-doped catalyst as compared with published data for a variety of Ni-containing catalysts based on the alumina support. In the reaction of ethanol steam reforming, the efficiency of catalysts on the doped supports is comparable, while exceeding that of Ni-containing supported catalysts reported in the literature. Coking stability was provided by a high oxygen mobility in the surface layers estimated by the oxygen isotope heteroexchange with CO. A high efficiency and coking stability were demonstrated in the reactions of methane dry reforming and ethanol dry and steam reforming in concentrated feeds for the honeycomb catalyst with a nanocomposite active component on the Fe-doped MgAlO support loaded on the FeCrAl-alloy foil substrate.
介孔 MgAlO 载体有望设计出用于天然气和生物燃料重整制合成气的高效且抗结焦催化剂。本工作旨在通过掺杂过渡金属阳离子(Fe、Cr、Ti)来防止浸渍负载的 Ni 和稀土阳离子(Pr、Ce、Zr)掺入其晶格中,并提供用于 CO 活化的额外位阻以防止结焦。采用 Pluronic P123 嵌段共聚物一锅蒸发诱导自组装法制备的掺杂 MgAlMeO(Me=Fe、Ti、Cr)介孔载体均为单相尖晶石。其比表面积在 115-200 m²/g 范围内变化,在浸渍负载 10 wt% PrCeZrO+(5 wt% Ni+1% Ru)支撑纳米复合材料活性组分后,降至 90-110 m²/g。对铁掺杂尖晶石的穆斯堡尔光谱证实,Fe 阳离子在晶格中空间均匀分布,没有团聚,主要位于八面体位置。吸附 CO 分子的傅里叶变换红外光谱用于估计金属位的表面密度。在甲烷干重整中,与未掺杂载体上的催化剂相比,观察到 MgAlO 载体掺杂的积极效果,即更高的周转频率,以及与基于氧化铝载体的各种含 Ni 催化剂的已发表数据相比,Cr 掺杂催化剂的最高有效一级反应速率常数。在乙醇蒸汽重整反应中,掺杂载体上催化剂的效率相当,而超过文献报道的含 Ni 负载催化剂。通过 CO 与氧同位素的异核交换估计表面层中氧的高迁移率,提供了结焦稳定性。在富含甲烷、乙醇干重整和蒸汽重整的反应中,负载在 FeCrAl 合金箔基底上的 Fe 掺杂 MgAlO 载体上的纳米复合材料活性组分的蜂窝状催化剂表现出高效和抗结焦稳定性。