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Al-SBA-15
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2018 · IF 3.141

Bifunctional Co/Al-SBA-15 Catalyst with Tunable Acidity for Selective Production of Aviation Fuel

Yuan Cai,Xiaofeng Xu,Hu Wang,Lei Wang,Lulu Chen,Rui Li,Jing Ding,Hui Wan,Guofeng Guan

Production of alternative, clean aviation fuel from biomass synthesis gas via Fischer–Tropsch (FT) synthesis has attracted much attention. In this paper, Al-SBA-15 supported cobalt catalysts with different Al/Si ratios were successfully prepared for the production of aviation fuel by FT synthesis. The physical and acidic properties of the Co/Al-SBA-15 catalysts were characterized by XRF, XRD, N2 adsorption–desorption, TEM, H2-TPR, 27Al NMR, NH3-TPD, and Py-FTIR. The formation of long-chain hydrocarbons was inhibited by the ordered mesoporous structure. Fischer–Tropsch activity and selectivity were demonstrated to be affected by the acidity of the Al-SBA-15 supports. The selectivity turned to lighter iso-paraffin products. Co-based catalyst with Al/Si ratio of 0.01 exhibited the highest selectivity (52.4%) for aviation fuel (C8–C18 products) and much higher ratio of iso-paraffin/normal-paraffin (iso/n) (20.2%). This study might provide useful information for the selective production of aviation fuel via FT synthesis.

研究领域: 化学工程 · 能源科学
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FUEL · 2019 · IF 5.128

Hydrodeoxygenation of lignin-derived phenols to produce hydrocarbons over Ni/Al-SBA-15 prepared with different impregnants

Xiangping Li,Jianguang Zhang,Bin Liu,Juping Liu,Chuanbin Wang,Guanyi Chen

Non-noble metal(s)-based mesoporous catalysts are one of the promising catalysts for aqueous phase hydrodeoxygenation of lignin-derived phenols to produce hydrocarbons. In this paper, Ni/Al-SBA-15 was prepared through incipient wetness impregnation method and the performance of eugenol hydrodeoxygenation over Ni/Al-SBA-15 was studied. The effect of incipient wetness impregnant on the performance of eugenol hydrodeoxygenation over Ni/Al-SBA-15 was investigated. The materials were characterized by XRD, N 2 -sorption, TEM, FTIR, Py-FTIR, XRF and ICP-MS. In comparison with the traditional incipient wetness impregnation using water as solvent, the activity of Ni/Al-SBA-15 was significantly improved by using ethanol as solvent during the process of incipient wetness impregnation. For Ni/Al-SBA-15, the quantity of total acid was decreased after loading nickel species which was mainly due to the decrease of Lewis acid sites. The strength of Lewis acid in Ni/Al-SBA-15 prepare with ethanol as impregant was enhanced. The yields of propyl cyclohexane and propylbenzene from aqueous phase hydrodeoxygeation of eugenol over Ni/Al-SBA-15-E were increased. The super catalytic behavior of Ni/Al-SBA-15-E was attributed to the synergistic effect between the stronger Lewis acid sites and the intact framework structure of Ni/Al-SBA-15-E.

CAS / MDL: 7784-27-2 13478-00-7
研究领域: 催化化学 · 可再生能源 · 材料科学
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JOURNAL OF SOLID STATE CHEMISTRY · 2019 · IF 2.291

Effect of organic template removal approaches on physiochemical characterization of Ni/Al-SBA-15 and eugenol hydrodeoxygenation

Xiangping Li,Han Yin,Jianguang Zhang,Juping Liu,Guanyi Chen

Template removing approaches can significantly impact the physiochemical properties of mesoporous molecular sieve materials. In order to better understand the relationship between template removing approaches and the properties of Ni/Al-SBA-15, four kinds of template removing approaches were introduced to remove the organic template from Al-SBA-15, respectively. The structural characteristics of these materials were analyzed by transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray fluorescence (XRF), powder X-ray diffraction (XRD), N 2 -sorption, Fourier transform infrared spectra (FT-IR), infrared spectra of pyridine adsorption (Py-FTIR), magic angle spinning-nuclear magnetic resonance (MAS-NMR), X-ray photoelectron spectroscopy (XPS) and gas chromatography-mass spectrometry (GC-MS). Ni/Al-SBA-15 of which the organic template was removed by two-step calcination method had the maximum specific surface area (619 ​m 2 /g). In contrast, Ni/Al-SBA-15 of which the organic template was removed using solvent extraction approaches had the lowest specific surface area (555 ​m 2 /g). The mesopore diameter of Ni/Al-SBA-15, using electric heating digestion method to remove the template, was significantly increased and the wall thickness was significantly decreased to 11.62 ​nm in comparison with the other samples. The selectivity of products during the process of eugenol hydrodeoxygenation was investigated. High hydrocarbons were obtained during catalytic hydrodeoxygenation over Ni/Al-SBA-15 of which the organic template was removed by using solvent extraction approaches. Compared with direct calcination process, two-step calcination was more effective in removing template and the corresponding catalyst was much more suitable for the hydrodeoxygenation process.

研究领域: 材料科学 · 催化化学
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RSC Advances · 2020 ·Vol. 10 ·期 5 ·2472-2482 · IF 3.119

MnOx dispersed on attapulgite derived Al-SBA-15: a promising catalyst for volatile organic compound combustion

Jie Meng,Fan Fang,Nengjie Feng,Hui Wan,Guofeng Guan

To improve the catalytic activity when utilizing metal oxides for the combustion of VOCs, Mn/Al-SBA-15 catalysts have been successfully synthesized through an emerging wetness impregnation technique involving Mn(NO3)2 on Al-SBA-15, which has been directly prepared from attapulgite by a hydrothermal method. Compared to Mn/SBA-15, which is prepared with TEOS as its silicon source, all the as-prepared Mn/Al-SBA-15 catalysts demonstrated enhanced catalytic performance in the oxidation of toluene. From this research, the 8% Mn/Al-SBA-15 catalyst presented the best catalytic performance, due to the high efficiency resulting from the high chemical valence of Mn4+. When the concentration of toluene was 2000 ppm, and the space velocity was 60 000 mL (g h)−1, 8% Mn/Al-SBA-15 could effectively reduce the T50 and T90 values of toluene to 201 and 278 °C, respectively; while the 8% Mn/SBA-15 catalyst could reduce the T50 and T90 values of toluene to 223 and 298 °C, respectively. A systematic investigation has been conducted to reveal the synergistic effects of Al doping and manganese loading on the enhanced catalytic performance. The experiments showed impressive results, demonstrating that Al doping can not only increase the surface acidity of SBA-15, but it can also be beneficial for achieving a uniform dispersion of MnOx on the surface and in the pores of Al-SBA-15, resulting in the enhancement of the catalytic performance.

CAS / MDL: 64-17-5 79-20-9 78-10-4
研究领域: 环境科学 · 催化 · 化学工程 · 材料科学
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MICROPOROUS AND MESOPOROUS MATERIALS · 2013 · IF 3.365

Tuning the pore structure of plug-containing Al-SBA-15 by post-treatment and its selectivity for C16 olefin in ethylene oligomerization

Sen Lin,Lei Shi,Hongpeng Zhang,Na Zhang,Xianfeng Yi,Anmin Zheng,Xuebing Li

Al-SBA-15 containing plug structures inside straight channels have been hydrothermally synthesized through a one-step synthesis strategy in an environmentally friendly acid-free medium. The effects of steaming, alkali, and acid post-treatments on the structural properties were investigated by powder X-ray diffraction (XRD), nitrogen adsorption–desorption at 77   K, transmission electron microscopy (TEM), scanning electron microscopy (SEM), FT-IR spectrum, 27 Al MAS NMR, and inductively coupled plasma (ICP) analyses. The presence of the plugs can significantly enhance structural stability against steaming or alkali post-treatments. Acid post-treatment can be a very simple and convenient technique for adjusting the textural properties of plug-containing Al-SBA-15, and especially for optimizing the accessibility to active sites. Acid post-treatment at the low temperatures of 313 and 323   K results in the formation of a larger specific surface area (905   m 2 /g) and pore volume (0.94   cm 3 /g) through an “open door” effect in the plugs, without eliminating any of the plugs from the channels. In particular, nearly half of the secondary micropores on the pore walls were preserved. In contrast, raising the acid post-treatment temperature further to 333 and 343   K caused a “closed doors” effect through the blockage of pores in the plugs by the extracted fragments. After loading with nickel, the catalyst exhibited a higher yield of C 10+ olefins in ethylene oligomerization , and more importantly, after steaming and acid post-treatments at higher temperatures, the samples showed shape selectivity for the C 16 olefin.

CAS / MDL: 7784-27-2 1310-73-2
研究领域: 材料科学 · 催化化学
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MICROPOROUS AND MESOPOROUS MATERIALS · 2016 · IF 3.349

Direct synthesis and characterization of pore-broadened Al-SBA-15

Shiyou Xing,Pengmei Lv,Junying Fu,Jiayan Wang,Pei Fan,Lingmei Yang,Zhenhong Yuan

A series of pore-broadened Al-SBA-15 samples were synthesized using a direct hydrothermal method . The effects of aluminum incorporation, assembling temperature, and co-solvent (1,3,5-trimethylbenzene (TMB)) content were investigated by low-angle XRD , N 2 adsorption and desorption isotherm analysis, SEM, TEM , NH 3 -TPD, FTIR, pyridine-IR, and 27 Al NMR. The results indicated that aluminum incorporation (Si/Al ratio = 10) increased the pore size of SBA-15 from 5.66 to 10.13 nm. A small pore size of 6.55 nm was observed at a low assembling temperature of 30 °C, attributing to the inadequate stretching of the molecular template. An increased pore size of 8.45 nm was obtained at an assembling temperature of 60 °C because of the partial hydrophobization of the hydrophilic groups , whereas a high temperature of 70 °C resulted in the generation of least ordered pores. The hydrophobic co-solvent TMB showed a significant broadening level as a result of its effective fusion into the hydrophobic micelle cores. A highly ordered pore framework with a pore size of 18 nm was obtained at a TMB/P 123 ratio of 0.25, which was found to be optimum. More or less TMB led to the generation of mesocellular silica-aluminum foams with a complete loss of regularity. The 27 Al NMR results showed that aluminum was mostly tetrahedrally coordinated. The NH 3 -TPD and pyridine-IR detection results indicated that a number of weak and medium acid sites (as Bronsted and Lewis acid sites) existed in Al-SBA-15 pore-broadened by TMB.

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RENEWABLE ENERGY · 2020 · IF 6.274

Investigation on catalytic hydrodeoxygenation of eugenol blend with light fraction in bio-oil over Ni-based catalysts

Guanyi Chen,Juping Liu,Xiangping Li,Jianguang Zhang,Han Yin,Zhenping Su

In this work, HZSM-5, Al-SBA-15 and Al-SBA-15/HZSM-5 were adopted as supporting materials for the nickel-based catalysts used in hydrodeoxygenation process. Incipient wetness impregnation method was employed to load nickel species onto these materials. The physicochemical characterization was carried out using advanced instruments. The effect of composition of nickel-based catalysts on hydrodeoxygenation (HDO) reaction was studied. Support materials of nickel-based catalyst have a significantly impact on HDO activity. The highest selectivity (67.9%) of propyl-cyclohexane was obtained over nickel based Al-SBA-15/HZSM-5 catalyst, and nearly all the eugenol was completely hydrodeoxygenated after reaction. The impact of light fractions existed in bio-oil on phenols upgrading process was investigated. The conversion of eugenol mixed with light fractions reached nearly 100% for all the reactions. Eugenol mixed with light fractions as reactant could reduce ring break reaction during hydrodeoxygenation process. The selectivity of alkanes remained nearly unchanged after adding ethylene glycol into the reactant. However, the selectivity of propyl-cyclohexane was significantly decreased by mixing furfural or acetic acid with eugenol as reactant.

研究领域: 化学工程 · 能源科学
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MICROPOROUS AND MESOPOROUS MATERIALS · 2021 · IF 5.455

High efficiency Al modified mesoporous SBA-15 catalyst for biomass-derived γ-valerolactone decarboxylation to butene

Haibiao Yu,Xiu Jia,Peng Wang,Ying Xiong,Weijun Shan,Congge Zhang,Zhimeng Song

A series of x wt%Al-SBA-15 catalysts prepared by modified wetness impregnation was investigated for γ-valerolactone (GVL) decarboxylation to butene . It was found that the impregnation of Al species not only remained the ordered mesoporous structure of parent SBA-15, but also created large amounts of Brønsted and Lewis acid sites on the surface of catalyst. The considerable amount of solid acid sites and the suitable Brønsted/Lewis acid ratio endowed 2.23 wt%Al-SBA-15 catalyst an excellent catalytic performance. Under the optimized conditions, the GVL conversion and butene yield can reach 99.8% and 96.6% at 320 °C, respectively. Mechanism studies indicated that the decarboxylation of γ-protonated PEA controlled speed of the whole reaction. Moreover, the catalytic activity of regenerated 2.23 wt%Al-SBA-15 catalyst was satisfactory after eight cycle tests, and the butene yield could still reach 92.2%.

CAS / MDL: 108-29-2
研究领域: 催化化学 · 生物质转化 · 材料科学
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CHINESE JOURNAL OF CHEMICAL ENGINEERING · 2017 · IF 1.174

Preparation of Ni2P/Al-SBA-15 catalyst and its performance for benzofuran hydrodeoxygenation

Tianhan Zhu,Hua Song,Xueya Dai,Hualin Song

The Al-doped Ni 2 P/Al-SBA-15 catalyst with high hydrodeoxygenation (HDO) activity was synthesized by temperature programmed reduction at a relatively low reduction temperature of 400   °C. The as-prepared catalyst was characterized by X-ray diffraction (XRD), H 2 temperature-programmed reduction (H 2 -TPR), X-ray photoelectron spectroscopy (XPS), transmission electron microscope (TEM), NH 3 temperature programmed desorption (NH 3 -TPD), N 2 adsorption–desorption and CO uptake. The effect of Al on benzofuran (BF) HDO performance was investigated. The result indicates that the incorporation of Al into the SBA-15 support can promote the formation of much uniform, smaller, highly dispersed Ni 2 P particles on the catalyst. The Al also contributes to suppress the enrichment of P and promote more exposed Ni sites on the surface. In addition, the incorporation of Al can enhance the acid strength. The total deoxygenated product yield over Ni 2 P/Al-SBA-15 reached 90.3%, which is an increase of 19.4%, when compared with that found for Ni 2 P/SBA-15 (70.9%).

CAS / MDL: 7791-20-0
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CELLULOSE · 2019 ·Vol. 26 ·期 15 ·8301-8312 · IF 3.917

Effect of nickel loading approaches on the structure and hydrodeoxygenation performance of Ni/Al-SBA-15

Li Xiangping,Liu Juping,Zhang Jianguang,Liu Bin,Ma Wenchao,Wang Chuanbin,Chen Guanyi

Lignocellulosic biomass-derived bio-oil is considered as a promising renewable biofuel. In this paper, incipient wetness impregnation method, ammonia grafting method and direct synthesis method were employed as nickel loading methods for the preparation of Ni/Al-SBA-15 catalysts. The effects of these nickel loading approaches on the structure and hydrodeoxygenation performance of Ni/Al-SBA-15 were studied. The structure of Ni/Al-SBA-15 was significantly influenced by the nickel loading methods, including the specific surface area, the pore volume, the wall thickness and so on. Nickel loading methods also affected the actual nickel content of nickel-based catalysts. Unsuccessful loading of nickel species was observed during the preparation of Ni/Al-SBA-15 using direct synthesis method. The conversion of eugenol and selectivity of products after hydrodeoxygenation in n -dodecane over Ni/Al-SBA-15 catalysts were investigated. Results showed that the conversion of eugenol nearly reached 100% for all the reaction, but the composition of product was significantly different when using different Ni/Al-SBA-15 as hydrodeoxygenation catalyst. The reaction pathway of eugenol hydrodeoxygenation in n -dodecane was also speculated in this paper. Graphic Effects of nickel loading approaches on the structure and hydrodeoxygenation performance of Ni/Al-SBA-15 were investigated. For the liquid phase hydrodeoxygenation of eugenol to hydrocarbon, catalysts prepared by ammonia grafting method exhibited the highest catalytic activity.

研究领域: 催化化学 · 可再生能源 · 生物质转化 · 材料科学
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Catalysis Science & Technology · 2020 ·Vol. 10 ·期 8 ·2443-2451 · IF 5.721

Highly-efficient Ru/Al–SBA-15 catalysts with strong Lewis acid sites for the water-assisted hydrogenation of p-phthalic acid

Cong Mao,Jingwei Zheng,Babasaheb M. Matsagar,Ranjith Kumar Kankala,Tansir Ahamad,Yucheng Yang,Kevin C.-W. Wu,Xueqin Zhang

Ruthenium nanoparticles supported onto aluminum-doped mesoporous silica catalysts (Ru/Al–SBA-15) are fabricated using hydrothermal and impregnation methods for catalysis application. The Ru/Al–SBA-15-3 catalyst at a Si/Al molar ratio of 3 exhibited excellent catalytic performance for the hydrogenation of p-phthalic acid with high conversion efficiency (100.0%) and cis-isomer selectivity (84.0%) in water. Moreover, this system displays exceptional stability and recyclability through preserving the conversion efficiency, as well as a cis-isomer selectivity of 90.2 and 83.3%, respectively, after reusing it fourteen times. Such an exceptional system can also be ideal for the hydrogenation of aromatic dicarboxylic acids and their ester derivatives in water. Strong Lewis acid sites due to doped Al species play significant roles in the hydrogenation reaction. Moreover, isotope labeling studies indicated that water molecules effectively participated in the hydrogenation reaction. Hydrogen and water contributed half of the hydrogen atoms for this hydrogenation reaction. In the end, a plausible mechanistic pathway for the hydrogenation of p-phthalic acid using the Ru/Al–SBA-15-3 catalyst in water is proposed.

研究领域: 催化化学 · 材料科学 · 有机化学
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INDUSTRIAL CROPS AND PRODUCTS · 2022 · IF 6.449

Regulating aromatic hydrocarbon components from catalytic pyrolysis of corn cob lignin with a tailored HZSM-5@Al-SBA-15 hierarchical zeolite

Shaoqing Wang,Zhihe Li,Weiming Yi,Peng Fu,Xueyuan Bai

Catalytic pyrolysis of corn cob lignin were preformed using a tailored HZSM-5 @Al-SBA-15 hierarchical zeolite for the production of value-added aromatic hydrocarbon. Resulted showed that the highly ordered two-dimensional p6mm mesoporous shell could uniformly form on the surface of HZSM-5 core phase. The porosity and acidity of the HZSM-5 @Al-SBA-15 could be tailored by adjusting the TEOS/HZSM-5 mass ratio in the synthesis process. The aromatic hydrocarbon components regulated due to pre-cracking and enhanced diffusion via the mesoporous shell, as well as the retained shape-selectivity of the HZSM-5 core. Herein, the relative content of MAHs reached 45.02% with fewer poly-aromatic hydrocarbons (PAHs) of 25.91% when the TEOS/HZSM-5 mass ratio of 1.0. However, the length of the diffusion path had a certain impact on the anti-coking behavior. The catalytic stability of the hierarchical zeolites was also improved, with less coke formation than HZSM-5 alone. This work demonstrates that using a tailored hierarchical zeolite to regulate aromatic hydrocarbon components is feasible, and provide a reference for the practical application of agricultural crop wastes.

研究领域: 能源与环境科学 · 化学工程
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