介孔材料
热液循环
对偶(语法数字)
联轴节(管道)
材料科学
水热合成
化学工程
模板方法模式
纳米技术
化学
催化作用
复合材料
有机化学
艺术
文学类
工程类
作者
Yufan Mo,Chunxia Che,Zhixin Li,X.B. Zhao,Kailong Liu,Bo Yang,Xiang-Dong Ren,Luis Alberto Estudillo‐Wong,Jiazhong Zang,Guan Jun,Yongjun Feng
标识
DOI:10.1021/acs.iecr.4c02529
摘要
Maintaining an optimized pore structure of the spherical alumina support after hydrothermal treatment is crucial for catalytic efficiency, as the pore structure is intricately linked to the dispersion of catalytically active components and the diffusion of reactants. In this work, a unique mesoporous–macroporous spherical γ-Al2O3 material (γ-Al2O3-CD) with a reduced amount of surface hydroxyl groups was successfully synthesized to address pore blockages and enhance hydrothermal stability. Dodecane and hydrophilic-modified activated carbon were used as dual-template agents and, as a result, γ-Al2O3-CD exhibits a distinctive mesoporous–macroporous structure, which is beneficial for specific surface area and stability. The mercury intrusion porosimetry (MIP) specific surface area is measured to be 256 m2·g–1, with a considerable pore volume of 0.62 mL·g–1 and an impressive porosity of 58.4%. In contrast, untreated γ-Al2O3 possesses only a specific surface area of 204 m2·g–1 and a pore volume of 0.40 mL·g–1. Additionally, the abundant pore structure greatly facilitates precursor dehydration, leading to the formation of γ-Al2O3. Remarkably, the γ-Al2O3 content in γ-Al2O3-CD reaches an impressive 70.7%, with a chemical shift of μ2-OH at 1.31 ppm, resulting in a decreased number of surface hydroxyl groups and ultimately enhanced hydrothermal stability. Even after a 120 h hydrothermal treatment, the MIP specific surface area remains virtually unchanged at 255 m2·g–1.
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