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JOURNAL OF POROUS MATERIALS · 2015 ·Vol. 23 ·期 2 ·529-537 · IF 1.108

Rapid synthesis of tunable-structured short-pore SBA-15 and its application on CO2 capture

Ma Beibei,Zhuang Linzhou,Chen Shuixia

The well-ordered hexagonal short-pore SBA-15 (SSBA-15) has been successfully synthesized via an energy-efficient process under the microwave-hydrothermal condition, in which the formation duration [stirring duration (ripening step) and microwave-hydrothermal treatment duration (aging step)] has been greatly decreased from 48 h for conventional hydrothermal treatment to <2 h. The extension of the ripening duration led to the evidently improved uniformity and regularity of particles while the increase of aging duration resulted in less intrawall pores and more structural mesopores. The optimal condition to get highly ordered SSBA-15 in this work was the duration of 2 h for both steps, and the SSBA-15 obtained was composed of cuboid-like particles, whose pore length was ca. 450 ± 50 nm and pore size was around 10 nm. The SSBA-15 was modified with different amine agents to prepare solid amine adsorbent, the obtained adsorbents showed considerable CO 2 adsorption ability, indicating that this fast-prepared SSBA-15 can be a promising support of CO 2 adsorbents.

CAS / MDL: 124-18-5 78-10-4
研究领域: 材料科学 · 环境科学
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JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY · 2018 ·Vol. 316 ·期 1 ·49-59 · IF 1.181

Granulation of short channel SBA-15 adsorbent and application for the removal of U(VI) by packed column

Ji Guojia,Zhu Guiru,Wang Xingjun,Wei Yulin,Wu Hui,Yuan Junsheng,Gao Congjie

In order to reduce the loss of particles during the cycling operation, a technology for the granulation of short channel SBA-15 adsorbent was developed. The adsorption behavior of obtained granules was studied under various factors including initial pH value, contact time in different initial concentration and acid stability by batch experiments. A continuous packed column loaded with granules was performed to remove U(VI) from aqueous solution. The uranium concentration was highly enriched than feed solution. The granules packed in column exhibited excellent reusability through cycling test. The result showed promising application prospect in the uranium extraction from aqueous solution.

CAS / MDL: 9002-86-2
研究领域: 材料科学 · 环境科学 · 核化学
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CHINESE JOURNAL OF CHEMICAL ENGINEERING · 2021 · IF 3.171

Coupling effect of bifunctional ZnCe@SBA-15 catalyst in 1,3-butadiene production from bioethanol

Zheng Wang,Sijia Li,Shengping Wang,Jiaxu Liu,Yujun Zhao,Xinbin Ma

A series of bifunctional ZnCe@SBA-15 catalysts with different Zn/Ce ratios were prepared by a solid-state grinding strategy and used in the conversion of ethanol to 1,3-butadiene (ETB). For the supported metal oxides, ZnO serves as the active sites for the dehydrogenation of ethanol, and CeO 2 promotes the aldol-condensation reaction. Based on the results of Py-FTIR and NH 3 -TPD, it suggests that the yield of 1,3-butadiene is positively correlated with the number of weak Lewis acid sites on the catalyst surface, given their benefit for aldol-condensation reactions. The catalyst with an optimal Zn/Ce ratio of about 1:5 has the highest concentration of weak Lewis acid. Coupling with the ZnO sites, it contributes to a 98.4% conversion of ethanol and a 45.2% selective of 1,3-butadiene under relatively mild reaction conditions (375 °C, 101.325 kPa, and 0.54 h −1 ).

CAS / MDL: 10196-18-6
研究领域: 催化化学 · 可再生资源化学
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FUEL · 2016 · IF 3.611

Catalytic adsorptive desulfurization of model diesel fuel using TiO2/SBA-15 under mild conditions

Xiaoling Ren,Guang Miao,Zhiyong Xiao,Feiyan Ye,Zhong Li,Haihui Wang,Jing Xiao

This study investigates catalytic adsorptive desulfurization (CADS) of model diesel fuel using TiO 2 /SBA-15 under mild conditions. The TiO 2 /SBA-15 was prepared by a facile incipient wetness impregnation method and characterized by N 2 adsorption and X-ray diffraction. The CADS referred to ADS performance were evaluated in a batch reactor. High desulfurization uptake of 12.7   mg/g was achieved at low sulfur concentration of 15   ppmw-S by TiO 2 /SBA-15 under CADS, which was two-magnitude higher than that under ADS without the in-situ catalytic oxidation of dibenzothiophene. Kinetic results suggested that the CADS equilibrium over TiO 2 /SBA-15 was reached fast in 0.5   h. In the CADS–TiO 2 /SBA-15 system, the TiO 2 loading, cumene hydroperoxide/dibenzothiophene ratio and CADS temperature were optimized to be 10   wt%, 2, and 35   °C, respectively. Furthermore, desulfurization tests in 5 consecutive CADS-regeneration cycles suggested that the bi-functional TiO 2 /SBA-15 can be regenerated by acetonitrile washing followed with oxidative air treatment. The CADS–TiO 2 /SBA-15 mechanism went through the oxidation of DBT to oxidized DBTO 2 over TiO 2 /SBA-15 by cumene hydroperoxide, which was followed by the adsorption of the oxidized DBTO 2 over TiO 2 /SBA-15. The superior desulfurization uptake at low sulfur concentration range, fast adsorption kinetics, excellent regenerability, operation at mild conditions, and facile and low-cost adsorbent synthesis make the CADS–TiO 2 /SBA-15 system an effective and economic desulfurization approach for ultra-clean fuel production.

CAS / MDL: 80-15-9
研究领域: 化学工程 · 材料科学 · 环境科学
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Journal of Materials Chemistry A · 2015 ·Vol. 3 ·期 18 ·9789-9798 · IF 7.443

Efficient removal of lead from highly acidic wastewater by periodic ion imprinted mesoporous SBA-15 organosilica combining metal coordination and co-condensation

Rong He,Weiming Li,Dayi Deng,Wensen Chen,He Li,Chaohai Wei,Youwen Tang

In order to develop a highly efficient method for direct removal of lead from acidic wastewater (pH 2.0), we introduce a novel highly ordered Pb2+ imprinted mesoporous silica (PbIMS) SBA-15 combining co-condensation and functionalized iminodiacetic acid (IDA). Fourier transform infrared spectroscopy (FTIR) and energy-dispersive X-ray (EDX) analysis provided the components of PbIMS. The solid-state 13C NMR spectra demonstrated the successful embedment of IDA in the mesoporous silica. Furthermore, X-ray photoelectron spectroscopy (XPS) analysis confirmed that Pb2+ was coordinated by the N atom and carboxyl O atom of IDA. The results of transmission electron microscopy (TEM), small angle X-ray diffraction (XRD) and N2 adsorption–desorption measurement confirmed that the PbIMS preserved a highly ordered hexagonal P6mm mesostructure. The Brunauer–Emmett–Teller (BET) surface area was 762 m2 g−1. The saturated adsorption capacity of PbIMS toward lead reached up to 103 mg g−1 at pH 2.0, which was greater even than that of the simply modified SBA-15 by IDA at pH 4.5. The values of selectivity coefficients of PbIMS for six competing metal ions ranged from 67.3 to 12.7. The adsorption of Pb2+ reached equilibrium within 7 min. The adsorption efficiency of PbIMS was above 93% after six extraction–stripping cycles. The investigation conducted with real samples of strongly acidic wastewater demonstrated the ability of PbIMS to efficiently remove lead below the current China regulatory standard.

研究领域: 环境科学 · 材料科学
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Journal of Environmental Chemical Engineering · 2022 · IF 7.968

Highly active and stable Cu-MnO/SBA-15 catalyst for hydrogenation of acetic acid to ethanol: Experimental and DFT studies

Xiuqin Dong,Jianhang Tian,Junwei Lei,Yifei Chen

Copper as a non-noble metal catalyst has great prospects in the hydrogenation of acetic acid to ethanol. In this paper, Cu-MnO/SBA-15 catalysts with highly catalytic performance and stability were prepared. The mechanism was elucidated by experiments and DFT calculations . The Cu and MnO were coexistent on reduced x Cu y Mn/SBA-15. Appropriate Cu/Mn ratio was beneficial for increasing the Cu surface area and reducing the size of Cu. The rate-controlled step was found and the MnO could effectively lower the difficulty of acetaldehyde formation by dioxyethylidene. DFT calculations indicated that the formation of ethyl acetate at the Cu-MnO interface was largely prevented. The optimal catalytic hydrogenation activity was obtained for 9Cu1Mn/SBA-15, with the conversion of acetic acid and selectivity of ethanol of 99.9% and 90.1%, respectively. The catalytic activity could remain within 72 h which was more stable than the original Cu-based catalyst.

CAS / MDL: 10031-43-3 10377-66-9
研究领域: 催化化学 · 理论化学
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Frontiers in Chemistry · 2025 · IF 4.2

Heterogeneous Fenton-like CuO-CoOx/SBA-15 catalyst for organic pollutant degradation: synthesis, performance, and mechanism

Jinwei Li,Yifei Wei,Qiang Liu,Huanhuan Guan,Chengchun Jiang,Xiaohui Sun

In this study, CuO-CoOx/SBA-15 catalysts were successfully synthesized via ultrasonic impregnation, and their performance in degrading nitrobenzene within a Fenton-like system was investigated. The catalyst materials were characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), inductively coupled plasma mass spectrometry (ICP-MS), scanning electron microscopy (SEM), transmission electron microscope(TEM) and energy-dispersive X-ray spectroscopy (EDS). The CuO-CoOx/SBA-15 catalysts featured well-distributed CuO-CoOx nanoparticles within the mesoporous SBA-15 support. Compared to CuO/SBA-15 and Co3O4/SBA-15 catalysts with similar microstructures, the CuO-CoOx/SBA-15 catalysts exhibited Cu-Co dual active centers and a higher abundance of redox-active sites. During catalytic degradation, H2O2 was continuously activated on the catalyst surface through efficient Cu+/Cu2+ and Co2+/Co3+ redox cycles. The experimental conditions (initial pH, catalyst dosage, and H2O2 dosage) were optimized, resulting in 99% nitrobenzene removal over a wide pH range (3.0–9.0). The primary mechanisms for the oxidation and subsequent removal of nitrobenzene in the CuO-CoOx/SBA-15-H2O2 system were identified as reactions with hydroxyl radicals (·OH).

研究领域: 环境科学 · 催化化学
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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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ENERGY & FUELS · 2013 · IF 2.853

Adsorptive Removal of Carbon Dioxide Using Polyethyleneimine Supported on Propanesulfonic-Acid-Functionalized Mesoporous SBA-15

Jie Liu,Dandan Cheng,Yue Liu,Zhongbiao Wu

One-step synthesized sulfonic-acid-functionalized SBA-15 (denoted as αSSBA-15) impregnated with polyethyleneimine (PEI) was used for CO2 capture in this study. The resulted sorbents were characterized via a range of analytical techniques, including transmission electron microscopy (TEM), 29Si magic angle spinning (MAS) nuclear magnetic resonance (NMR), infrared (IR), thermogravimetry–differential scanning calorimetry (TG–DSC), etc. Experimental results showed that the incorporation of propanesulfonic acid groups into the inner structure of the silica support had brought dramatic improvement in CO2 adsorption capacity, of which PEI/5SSBA-15 showed the highest CO2 adsorption amount. The main reason of this increased capacity could be attributed to the enhanced CO2 diffusion into bulk networks of PEI polymers because of its better dispersion in the pores of support, where the extended propanesulfonic acid groups on the inner surface could spatially disperse the subsequent loaded PEI molecules. Furthermore, the PEI/5SSBA-15 also exhibited superior stable cyclic adsorption/desorption performance compared to PEI/SBA-15, especially after 5 cycles. This was assumed because the enhanced surface acidity of PEI/5SSBA-15 anchored the NH2/NH groups through acid–base interaction, reducing the loss of active sites.

CAS / MDL: 100587-95-9
研究领域: 材料科学 · 环境科学
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ANALYTICAL AND BIOANALYTICAL CHEMISTRY · 2014 ·Vol. 407 ·期 2 ·509-519 · IF 3.578

Molecularly imprinted polymers based on SBA-15 for selective solid-phase extraction of baicalein from plasma samples

He Hongliang,Gu Xiaoli,Shi Liying,Hong Junli,Zhang Hongjuan,Gao Yankun,Du Shuhu,Chen Lina

Highly selective molecularly imprinted mesoporous silica polymer (SBA-15@MIP) for baicalein (BAI) extraction was synthesized using a surface molecular imprinting technique on the SBA-15 supporter. Computational simulation was used to predict the optimal functional monomer for the rational design of SBA-15@MIP. Meanwhile, high adsorption capacity was obtained when a suitable yield of molecularly imprinted polymers (MIPs) layer was grafted onto the surface of SBA-15. Characterization and performance tests of the obtained polymer revealed that SBA-15@MIP possessed a highly ordered mesoporous structure, reached saturated adsorption within 60 min, and exhibited higher sorption capacity to the target molecule BAI compared with non-imprinted mesoporous silica polymer (SBA-15@NIP) and SBA-15. Finally, SBA-15@MIP was successfully applied to solid-phase extraction (SPE) coupled with high-performance liquid chromatography and ultraviolet detection (HPLC-UV) for the determination of trace BAI in plasma samples. Mean recoveries of BAI through the molecularly imprinted solid-phase extraction (MISPE) sorbent, non-imprinted solid-phase extraction (NISPE) sorbent, and SBA-15 solid-phase extraction (SBA-15-SPE) sorbent were 94.4, 22.7, and 10.7 %, respectively, and the relative standard deviations were 2.9, 2.6, and 3.6 %, respectively. These results reveal that SBA-15@MIP as a SPE sorbent has good applicability to selectively separate and enrich trace BAI from complex samples. Synthesis procedure of SBA-15@MIP

CAS / MDL: 2530-85-0
研究领域: 分析化学 · 材料科学
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2022 · IF 7.139

Supporting high-loading Ni on SBA-15 as highly active and durable catalyst for ammonia decomposition reaction

Ze-Wei Wu,Jing Xiong,Cun-Wen Wang,Yuan-Hang Qin

Although supported Ni is generally considered the most active non-noble metal catalyst for decomposing NH 3 to produce CO x -free H 2 , its activity is not sufficient. Herein, supporting high-loading Ni on SBA-15 is explored to alleviate the low intrinsic activity issue of Ni. SBA-15 supports with tunable textual properties are synthesized to support Ni catalyst for NH 3 decomposition. Characterization shows that Ni catalyst with a loading close to 40 wt% supported on SBA-15 with the largest specific surface area (Ni/SBA-15-80) exhibits a NH 3 decomposition performance much better than those reported on other Ni-based NH 3 decomposition catalysts, resulting from its favorable textural properties and high Ni loading. In addition, Ni/SBA-15-80 shows excellent catalytic stability, with no activity degradation over an 80-h NH 3 decomposition test. This work reveals the importance of textural properties of support and Ni loading to NH 3 decomposition performance and can provide a new idea for synthesizing high-performance NH 3 decomposition catalysts.

研究领域: 材料科学 · 催化化学
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NANOTECHNOLOGY · 2020 ·Vol. 31 ·期 37 ·375603 · IF 3.551

Efficient synthesis of sub-5 nm Ag nanoparticles by the desorption effect of supercritical CO2 in SBA-15

Guoyue Qiao,Qinqin Xu,Aiqin Wang,Dan Zhou,Jianzhong Yin

Herein, the desorption effect of supercritical CO2 (scCO2) was utilized to obtain sub-5 nm Ag nanoparticles (NPs) with a high Ag loading in SBA-15. The size of the Ag NPs decreased from 3.54 ± 0.79 nm (Ag loading of 25.3 wt.% wt.%) to 2.38 ± 0.68 (Ag loading of 10.5 wt%) nm by changing the depressurization curve from 0.1 MPa min−1 (20–14 MPa) to 3 MPa min−1 (20–12 MPa). Meanwhile, the intensity of the crystalline Ag characteristic peaks was obviously higher than the latter sample from the x-ray diffraction (XRD) patterns. However, compared with the adsorption kinetics of the two precursors of AgNO3 and Cu(NO3)2 on SBA-15, under the same deposition and depressurization conditions, when the two depositional systems used water as a co-solvent, the time taken to reach the adsorption equilibrium of Ag+ on the supports was longer than the time taken by Cu2+, which existed in the water as [Cu(H2O)4]2+. The surface of SBA-15 was hydrophilic, and then the interaction of Ag+ and the surface was weaker compared with Cu2+, making Ag+ highly dispersed on the surface under the scCO2 desorption effect. After calcination, the size of the Ag NPs decreased, but the morphology of CuO was mainly characterized by nanorods (NRs). Moreover, by comparing the experiments of wetness impregnation, the dispersion ability of the bulk scCO2 of the reactor was inefficient for Ag+ adsorbed on the channels in the depressurization process.

研究领域: 材料科学 · 化学工程
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