Catalysis Science & Technology
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2014
·Vol. 4
·期 11
·4010-4019
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IF 4.76
Chao Lin,Kai Tao,Hongbo Yu,Dayin Hua,Shenghu Zhou
Molybdenum-doped mesoporous SBA-15, mesoporous SBA-15-supported MoO3/SBA-15, and traditional silica-supported MoO3/SiO2 were successfully synthesized. Various techniques, such as XRD, TEM, BET, UV-DRS, Raman, XPS and IR, were used to characterize the above obtained materials. The studies of TEM, XRD and BET confirmed that the highly ordered mesoporous structure of SBA-15 was maintained in the doped Mo-SBA-15 whereas supported MoO3/SBA-15 showed a significant reduction in surface area due to the deposition of MoO3 nanoparticles into the SBA-15 channels. XPS studies revealed that a high concentration of Mo5+ species appeared in doped Mo-SBA-15 whereas supported MoO3/SBA-15 and MoO3/SiO2 only contained Mo6+ species. The metathesis reaction of 1-butene and ethene to propene was used to evaluate the catalytic performance of Mo-containing materials. The doped Mo-SBA-15 illustrated a superior catalytic performance over the supported MoO3/SBA-15 and MoO3/SiO2 catalysts. The enhancement of catalytic performance for doped Mo-SBA-15 was assigned to the incorporation of Mo species into the SBA-15 framework. Due to the doping method, Mo-SBA-15 exhibited a well-ordered mesoporous structure, a high surface area, and a high concentration of Mo5+ species, which is beneficial to the catalytic performance for metathesis reactions.
研究领域:
材料科学
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催化化学
✓ 已验证
产品关联
DOI
高影响因子
ChemCatChem
·
2016
·Vol. 8
·期 6
·1199-1207
·
IF 4.724
Lan-Lan Lou,Shanshan Li,Huanling Du,Jiong Zhang,Wenjun Yu,Kai Yu,Shuangxi Liu
Graphical Short support : A short-mesochannel SBA-15 material is applied to the immobilization of a chiral 9-amino epicinchonine iridium catalyst, which exhibit excellent catalytic activity and notably improved enantioselectivity for the asymmetric transfer hydrogenation of aromatic ketones. A short-mesochannel SBA-15 material functionalized with propylthiol groups was prepared by co-condensation and applied to the immobilization of chiral 9-amino epicinchonine. After complexing with [Ir(cod)Cl] 2 (cod=1,5-cyclooctadiene), these mesoporous materials were evaluated as catalysts for the asymmetric transfer hydrogenation of aromatic ketones. Higher enantioselectivities and comparable, or even higher, catalytic activities were achieved compared with the free catalyst. Both the short mesochannel and co-condensation approach for short-mesochannel SBA-15 materials functionalized with propylthiol groups, [SSBA-SH( x )] materials were demonstrated to contribute to the excellent catalytic performance. In addition, the catalyst SSBA-AEC(5)/Ir (AEC=9-amino epicinchonine), with low 3-mercaptopropyltrimethoxysilane (MPTMS) content, showed the best catalytic performance; a high enantiomeric excess of 84 % (homogeneous ee =60 %) along with a conversion of 97 % was achieved within 1 h for asymmetric transfer hydrogenation of acetophenone. Moreover, these immobilized catalysts showed high stability during the reaction and could be recovered for reuse.
研究领域:
材料化学
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催化化学
✓ 已验证
产品关联
DOI
高影响因子
MICROPOROUS AND MESOPOROUS MATERIALS
·
2018
·
IF 3.649
Meng Zhang,Bingxian Chu,Guoying Li,Jianze Xiao,Haowen Zhang,Yujie Peng,Bin Li,Peng Xie,Minguang Fan,Lihui Dong
A series of triethanolamine-modified mesoporous SBA-15 catalysts were synthesized by a facile one-pot process, and used as the catalyst for the synthesis of cyclic carbonates through the cycloaddition of CO 2 with epoxides. The properties of catalysts were characterized by nitrogen adsorption–desorption, elemental analysis (EA), Fourier transform infrared (FT-IR) spectra, Magic angle spinning nuclear magnetic resonance (MAS NMR), X-ray diffraction (XRD), scanning electron microscope (SEM), and transmission electron microscopy (TEM), and the results suggested that triethanolamine (TEA) had been successfully immobilized on SBA-15. It was highly active in the cycloaddition reaction, in which the maximum yield of PC could achieve 93.47% under the conditions as follow: catalyst amount of 0.20 g, reaction temperature of 110 °C, reaction pressure of 2.0 MPa and reaction time of 4 h. Notably, the catalyst can be easily recovered by filtration, and it can be retained most of its catalytic stability and activity after five recycling times. On the basis of the experimental results, the interactions between the catalysts and the substrates were studied by DFT calculations, and the possible mechanism for the reaction was proposed.
研究领域:
材料科学
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催化化学
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
COMPOSITES PART B-ENGINEERING
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2020
·
IF 7.635
Beibei Ma,Rijia Lin,Hui He,Qinghua Wu,Shuixia Chen
Hydrothermal is common process for synthesizing well-ordered mesoporous silica, however, it costs time and energy simultaneously. To improve the efficiency of synthesis process, it is necessary to propose a facile synthesis strategy with less time and energy requirement. In this study, an innovative non-hydrothermal method using NH 3 ∙H 2 O as catalyst after ripening step is developed to prepare SBA-15 with short mesochannels (SSBA-15) for the first time. The synthesis period of SSBA-15 framework was extremely shortened within 40 min under the optimized conditions (30 min of ripening step and 25% of NH 3 ∙H 2 O concentration), while obtained material exhibits well-ordered hexagonal pore structure and fine particle morphology of SSBA-15 (pore length of 250 ± 50 nm and mesopore size of 9.8 nm). This method can also be employed to synthesize conventional SBA-15 successfully. Moreover, the application of SSBA-15 as support of solid amine adsorbents on CO 2 adsorption and well-fitting of experimental CO 2 adsorption data with Avrami and intraparticle diffusion models reveal that the adsorbents combine the advantages of micro-mesoporous structure, short mesochannel and amine reagents (high affinity of CO 2 ), resulting in enhanced molecular diffusion, fast adsorption kinetics and high CO 2 adsorption capacity . Notably, the solid amine adsorbents exhibited excellent regeneration ability during ten adsorption-desorption cycles. This work opens up new opportunities in efficient preparation of materials that require hydrothermal process.
研究领域:
材料科学
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环境工程
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化学工程
✓ 已验证
产品关联
DOI
高影响因子
ACS Sustainable Chemistry & Engineering
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2022
·
IF 9.224
Yu Yin,Chunhui Ma,Wei Li,Sha Luo,Zhanshuo Zhang,Shouxin Liu
Facilitated isomerization of cellulose hydrolysis intermediate glucose without unexpected byproducts, which is the rate-determining step in the production of high-value-added biofuels, enables the efficient production of 5-hydroxymethylfurfural (5-HMF) from cellulose. In this work, considering the essential role of the acidity control and shape selectivity of a zeolite catalyst, a NiO-loaded mesoporous NiO/poly(vinyl pyrrolidone) (PVP)-phosphotungstic acid (HPA)@SBA-15 nanoreactor was prepared. This SBA-15 nanoreactor with a pore size of 5.47 nm reduced the concentration of byproducts formic acid (FA) and levulinic acid (LA) through shape selection for intermediates. Well-defined NiO nanoparticles (Ni-to-carrier mass ratio was 1:1) provided the NiO/PVP-HPA@SBA-15 nanoreactor a high Lewis acidity of 99.29 μmol g–1 for glucose catalytic isomerization, resulting in an increase in total reducing sugar (TRS) yield by 5 times. Such a nanoreactor remarkably improved the reaction efficiency of 5-HMF production from cellulose (a 5-HMF selectivity of 95.81%) in the 1-butyl-3-methylimidazolium chloride ([BMIM]Cl)/valerolactone (GVL) biphasic system.
研究领域:
化学工程
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催化
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纳米技术
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生物燃料
✓ 已验证
产品关联
DOI
高影响因子
ACS Nano
·
2024
·
IF 15.8
Qingyun Kang,Xiaofang Zhang,Qianyue Feng,Lin Zhang,Mingyu Chu,Chaoran Li,Panpan Xu,Muhan Cao,Le He,Qiao Zhang,Jinxing Chen
Hydro-depolymerization presents a promising avenue for transforming plastic waste into high-value hydrocarbons, offering significant potential for value-added recycling. However, a major challenge in this method arises from kinetic limitations due to insufficient hydrogen concentration near the active sites, requiring optimal catalytic performance only at higher hydrogen pressures. In this study, we address this hurdle by developing “hydrogen bubble catalysts” featuring Ru nanoparticles within mesoporous SBA-15 channels (Ru/SBA). The distinctive feature of Ru/SBA catalysts lies in their capacity for physical hydrogen storage and chemically reversible hydrogen spillover, ensuring a timely and ample hydrogen supply. Under identical reaction conditions, the catalytic activity of Ru/SBA surpassed that of Ru/SiO2 (no hydrogen storage capacity) by over 4-fold. This substantial enhancement in catalytic performance provides significant opportunities for near atmospheric pressure hydro-depolymerization of plastic waste.
研究领域:
材料科学
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环境科学
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化学工程
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催化
✓ 已验证
DOI
PubMed
高影响因子
APPLIED ORGANOMETALLIC CHEMISTRY
·
2019
·Vol. 33
·期 6
·e4874
·
IF 3.259
Yingpeng Huo,Jiwen Hu,Shudong Lin,Xingming Ju,Yanlong Wei,Zhenzhu Huang,Yangfei Hu,Yuanyuan Tu
Reported herein is an easy-to-prepare novel heterogeneous catalyst of platinum complexes bearing binary ligands of bidentate naphthalenolimine and cyclo-1,5-octadiene that are anchored onto mesoporous silica SBA-15. The presence of the binary ligands not only stabilized the platinum, but also enabled the platinum atoms to form nanoclusters with diameters of ca 1 nm, and led to high platinum loading (8.69 wt%). Moreover, the platinum catalyst exhibited high catalytic activity towards hydrosilylation of terminal alkenes and styrene with silanes under mild and solvent-free conditions, with excellent regioselectivity.
研究领域:
催化
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材料科学
·
无机化学
✓ 已验证
产品关联
DOI
高影响因子