Desalination and Water Treatment
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2024
·
IF 1
Qinglong Luo,Lei Liu,Ruiqiang Dong,Zhongfu Cheng,Mingzhe Dong,Zhijian Wu,Jun Li,Xueli Huang
ABSTRACT The removal of boron from aqueous solution and the enrichment of boron from salt lake have attracted more attention. In this work, organo-inorganic hybrid mesoporous boron adsorbents were synthesized by tris(hydroxymethyl)methyl aminomethane (TRIS) grafted onto the meso-porous SBA-15, SBA-16 and MCM-41, respectively. And the structures are characterized by infrared, scanning electron microscopy, energy-dispersive X-ray, mapping, X-ray diffraction, point of zero charge, and Marvin laser particle size analyzer. The results showed that TRIS was successfully grafted onto SBA-15, SBA-16, and MCM-41. The adsorption isotherm and adsorption kinetics were best fitted with Langmuir model and pseudo-second-order rate equation, respectively. The adsorption capacity of the three adsorbents was 15.28, 15.70 and 14.17 mg/g, respectively. And the same functional group has little influence on the boron adsorption capacity of different carrier adsorbents of the same type (organosilicon material). These adsorbents have highly selective adsorption of boron, and maintain good lifetime after adsorption–desorption for 5 times, and the dissolution loss rate of SBA-16-TRIS after ten cycles was 0.93%.
研究领域:
环境科学
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材料科学
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化学工程
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DOI
高影响因子
CHINESE JOURNAL OF CATALYSIS
·
2015
·
IF 1.964
Huimin Liu,Yuming Li,Hao Wu,Jiaxiong Liu,Dehua He
Organic compounds containing multiple hydroxyl groups, namely α-cyclodextrin and γ-cyclodextrin, were used as additives for promoting Ni dispersion on supported Ni/SBA-15 catalysts. Catalysts prepared using modified and unmodified impregnation methods were characterized using N 2 adsorption-desorption isotherms, X-ray diffraction, transmission electron microscopy, temperature-programmed reduction, and thermogravimetric analysis, and their catalytic performance in the CO 2 reforming of methane (CRM) to syngas was evaluated. The results show that compared with Ni/SBA-15 prepared using a conventional impregnation method, the cyclodextrin-modified catalysts had smaller NiO particles. They also exhibited higher catalytic activity and had stronger ability to resist carbon deposition in the CRM. Mechanistic studies showed that for the unmodified catalysts, Ni 2+ could migrate into the channels of SBA-15 as a result of concentration differences, and the Ni species were sintered during the following thermal treatment processes, and could not be well dispersed. In contrast, various types of complex were formed between Ni(NO 3 ) 2 and the cyclodextrins, and this would be favorable for Ni 2+ being taken into the channels of the SBA-15. The presence of cyclodextrins was beneficial to the mutual isolation of Ni species, and finally resulted in better dispersion of Ni species.
研究领域:
催化
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化学工程
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材料科学
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DOI
高影响因子
Environmental Science-Water Research & Technology
·
2022
·Vol. 8
·期 8
·1763-1776
·
IF 5.819
Di Li,Mingyang Long,Qianqian Zhao,Hongmiao Li,Qi Wen,Fang Song
Nanosized CoTiO3, NiTiO3 and Fe2TiO5 photocatalysts were synthesized by a simple sol–gel method successfully. However, they showed lower photocatalytic activity for the degradation of oxytetracycline hydrochloride under visible light irradiation. After the CoTiO3, NiTiO3 and Fe2TiO5 nanoparticles were loaded in the SBA-15 channels, the photocatalytic activity was enhanced obviously. In order to further enhance the removal efficiency of CoTiO3/SBA-15, NiTiO3/SBA-15 and Fe2TiO5/SBA-15, they were used to activate peroxymonosulfate under visible light irradiation. In particular, CoTiO3/SBA-15 could completely photodegrade oxytetracycline hydrochloride with the assistance of peroxymonosulfate in an hour. The influencing factors on activating peroxymonosulfate to degrade oxytetracycline hydrochloride were investigated in detail. In addition, the electron transfer and peroxymonosulfate activation mechanism for the efficient improvement in the photocatalytic performance were also proposed and proved by radical quenching experiments, electron spin resonance analysis, X-ray photoelectron spectroscopy, transient photocurrent responses and cyclic voltammetry. It was found that the combined activation effects of photogenerated electrons and transition metals on peroxymonosulfate to produce sulfate radicals could enhance the degradation efficiency obviously. This study could provide a new way for the synergetic effect of photocatalysis and peroxymonosulfate activation by transition metal to be used for efficient photocatalytic degradation in the field of antibiotic removal.
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Catalysts
·
2021
·Vol. 11
·期 6
·710
·
IF 4.146
Linmeng Huo,Tian Wang,Keng Xuan,Lei Li,Yanfeng Pu,Chenxin Li,Congzhen Qiao,Hao Yang,Yan Bai
The adsorption and activation of both CO2and methanol are mainly affected by the distance of the Lewis acid site, Zr4+, and Lewis base, Zr4+/O2−, of the Zr-based catalysts. In this paper, Zr-incorporated SBA-15 (Zr-SBA-15) and Zr-grafted SBA-15 (Zr/SBA-15) catalysts were prepared with different Zr environments, and were analyzed with N2adsorption–desorption isotherms, X-ray diffraction, UV-vis spectra, and XPS. It was proposed that Zr-SBA-15 catalyst with Si-O-Zr-OH and Zr-O-Si-OH structure exhibited non-adjacent sites between Zr4+and Zr4+/O2−, while Zr/SBA-15 catalyst with Zr-O-Zr-OH structure showed neighboring sites between Zr4+and Zr4+/O2−. Furthermore, the Zr/SBA-15 catalyst exhibited good catalytic activity, while no DMC was detected over the Zr-SBA-15 catalyst at the same reaction conditions. For combined in situ infrared and catalytic performance, it was indicated that the methanol and CO2could be activated to form DMC, only when the Zr4+and Zr4+/O2−sites existed and were adjacent to each other in the Zr-O-Zr-OH of Zr/SBA-15 catalyst.Keywords:dimethyl carbonate;in situ FTIR spectra;ZrO2-grafted SBA-15;Zr-incorporated SBA-15;carbon dioxide
研究领域:
催化化学
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环境科学
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DOI
高影响因子
Reaction Kinetics Mechanisms and Catalysis
·
2018
·Vol. 125
·期 2
·923-936
·
IF 1.515
Shiwei Wang,Qibao Wang
Ytterbium triflate was immobilized on SBA-15 via chemical grafting and co-condensation and the catalytic performance of the immobilized ytterbium triflate for the selective conversion of glucose into lactic acid was investigated in this paper. The characterization results showed that ytterbium triflate was immobilized on SBA-15 successfully. It was found that the immobilized ytterbium triflate catalyst can catalyze the transformation of glucose into lactic acid effectively. The 58.01% yield of lactic acid was obtained from glucose at 200 °C. The HPLC analysis results of the products showed that the glyceraldehyde might act as an intermediate for the formation of lactic acid during the reaction. The immobilized ytterbium triflate catalyst was recycled for more than five times without noticeable loss in activity.
研究领域:
生物化学
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催化化学
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DOI
高影响因子
MICROPOROUS AND MESOPOROUS MATERIALS
·
2016
·
IF 3.349
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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高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
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2020
·
IF 4.939
Zhang Haocui,Xiao Zhourong,Yang Mei,Tian Yajie,Li Guozhu,Zhang Xiangwen,Liu Guozhu
As the only H 2 resource on aircraft from the steam reforming of the jet fuels on board, catalytic steam reforming of JP-10 (one of Jet fuels) over nickel-based catalyst Ni/SBA-15 were first carried out in a fixed bed tube reactor to produce hydrogen on-site or on board. A series of Ni/SBA-15 catalysts with different Ni content (3, 5, 8 and 10.8 wt%) were prepared by a modified incipient wetness impregnation method with addition of sucrose as ligand. And the effect of operation conditions of temperature (630–700 °C), nickel loading, liquid hour space velocity (LHSV = 5, 10, 15 ml/g cat ·h), steam to carbon molar ratio (S/C = 3, 5) on the catalytic activity and selectivity was investigated. It was found that 8Ni/SBA-15 was the optimal catalyst for steam reforming of JP-10 even with a higher LHSV and fuel gas concentration, and approximately 100% conversion of JP-10 with over 80% selectivity to hydrogen under the recommended experimental conditions of 680 °C, S/C of 5, LHSV of 10 ml/g cat ·h. The catalytic activity of 8Ni/SBA-15 dropped slowly to 84% after 6.5 h in the stability test and the carbon deposited was less with just 6% mass loss from TGA measurement (coke deposition rate 0.01g C /g cat h), which ascribed to possible reasons including confine effect of mesochannel of SBA-15, strengthened structure of mesochannels due to embeded Ni particles, and higher temperature to suppress the main carbon producing reaction.
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高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2019
·
IF 4.175
Bolong Jiang,Tianhan Zhu,Hua Song,Feng Li
The Fe-doped Ni 2 P/Fe-SBA-15 was prepared by the temperature programmed reduction method at a relative low temperature of 673 K. The effect of Fe on the catalytic performance for benzofuran (BF) hydrodeoxygenation (HDO) and dibenzothiophene (DBT) hydrodesulfurization (HDS) were investigated. The catalysts were characterized by means of X-ray diffraction (XRD), N 2 adsorption-desorption, inductively coupled plasma mass spectrometry (ICP-MS), X-ray photoelectron spectroscopy (XPS), temperature-programmed desorption of ammonia (NH 3 -TPD), and transmission electron microscope (TEM) and CO uptakes. The results indicate the incorporation of Fe into SBA-15 contributes to the exposure of smaller Ni 2 P particles (5.6 nm) with an uniform dispersion, along with enhancement of weak and medium acid strengths . Compared with Ni 2 P/SBA-15, the Fe-doped Ni 2 P/Fe-SBA-15 exhibited a much higher BF conversion of 91.7% with an improved total deoxygenated product yield of 83.3%. The excellent HDO performance of Ni 2 P/Fe-SBA-15 can be ascribed to the exposure of highly-dispersed smaller Ni 2 P particles. Meanwhile, the improved dehydration of 2-EtPh to EB and the high deoxygenated product selectivity can be attributed to the enhanced acidity. As compared to the Ni 2 P/SBA-15, the Fe-doped Ni 2 P/Fe-SBA-15 showed a higher DBT HDS activity of 96.3% with the BP formation at a great proportion of 90.3%, indicating that DBT was mainly transformed through the desulfurization pathway during HDS.
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高影响因子
Natural Products and Bioprospecting
·
2024
·Vol. 14
·期 1
·1-16
·
IF 4.8
Yang Ya-Ya,Jing Shun-Li,Shao Jia-Li,Chen Ji-Xuan,Zhang Wei-Feng,Wan Si-Yuan,Shen Yu-Ping,Yang Huan,Yu Wei
Functionalized mesoporous materials have become a promising carrier for enzyme immobilization. In this study, Santa Barbara Amorphous 15 (SBA-15) was modified by N-aminoethyl- γ -aminopropyl trimethoxy (R). R-SBA-15 was employed to purify and immobilize recombinant β -glucosidase from Terrabacter ginsenosidimutans (BgpA) in one step for the first time. Optimum pH of the constructed R-SBA-15@BgpA were 7.0, and it has 20 ℃ higher optimal temperature than free enzyme. Relative activity of R-SBA-15@BgpA still retained > 70% at 42 ℃ after 8-h incubation. The investigation on organic reagent resistance revealed that the immobilized enzyme can maintain strong stability in 15% DMSO. In leaching test and evaluation of storage stability, only trace amount of protein was detected in buffer of the immobilized enzyme after storage at 4 ℃ for 33 days, and the immobilized BgpA still maintained > 50% relative activity. It also demonstrated good reusability, with 76.1% relative activity remaining after fourteen successive enzymatic hydrolyses of epimedin A to sagittatoside A. The newly proposed strategy is an effective approach for the purification and immobilization of BgpA concurrently. In addition, R-SBA-15@BgpA was demonstrated to have high efficiency and stability in this application, suggesting its great feasibility and potential to produce bioactive compounds such as secondary glycosides or aglycones from natural products. Graphical Abstract
研究领域:
生物化学
·
酶工程
·
材料科学
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产品关联
DOI
PubMed
高影响因子
MICROPOROUS AND MESOPOROUS MATERIALS
·
2022
·
IF 5.876
Yi Liu,Yuhang Hu,Jiarong Zhang,Jingsheng Zhou,Zhengkun Zhang,Li Wang,Jinglai Zhang
Immobilized ionic liquids are one of the most popular catalysts for the cycloaddition of carbon dioxide (CO 2 ) and epoxides with some distinguished advantages. However, the harsh reaction condition, especially for the high reaction pressure, is still the obstacle for its large-scale application. A series of amino-functionalized pyrazolium ionic liquids are grafted on SBA-15 in this work. Among them, SBA-15-APMPzBr(20) exhibits the best catalytic activity achieving 97.6% product yield under 0.5 MPa CO 2 pressure at 100 °C by using 100 mg SBA-15-APMPzBr(20) for 10 h. No solvent is added in the catalytic system. Moreover, SBA-15-APMPzBr(20) exhibits the good recyclability and generality. Its excellent catalytic performance is attributed to the contribution from both immobilized ionic liquids and the SBA-15 supporter. Besides the mesoporous feature, the hydroxyl groups in SBA-15 promote the ring-opening of substrate, which is testified by the experimental measurements and density functional theory calculations.
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高影响因子
MICROPOROUS AND MESOPOROUS MATERIALS
·
2025
·
IF 4.7
Yuhang Huang,Pingwei Yang,Shaokai Sun,Liyun Mao,Yunyun Zhou,Ying Liu,Juanjuan Peng,Lingzhi Zhao
Porous silica materials can serve as hemostats, offering a promising approach to promote the coagulation speed. The pore structure of porous silica is a critical property, which may influence the hemostatic effectiveness, though its exact role in the hemostasis process remains unclear. Given that the key structural parameters of porous silica, including pore size, surface area, and pore volume, exhibited strong interrelationships that significantly influence each other, we prepared porous silica with pore sizes ranging from 2.5 to 50 nm to study their hemostatic effects by both in vitro and in vivo assessments. The results demonstrated that the mesoporous material MCM-41 with small pore size (2.5 nm) and high specific surface area exhibited superior contact activation capability to the coagulation pathway. In contrast, the macroporous siliceous foam (MSF) with large pore size (50 nm) and large pore volume showed enhanced absorption of blood cells and proteins. The mesoporous SBA-15 with pore size of 5.3 nm displayed intermediate properties between the two materials. The in vivo experiments showed that among the three kinds of porous silica, the MCM-41 provided the highest pro-coagulant capacity in the tail transection rat model with minor bleeding, and the MSF performed the best hemostatic effect in the femoral artery injury rat model with spurting hemorrhage. Our study elucidates the role of pore structure of porous silica as hemostats, which may give hint to the design of such materials.
研究领域:
生物医学工程
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材料科学
·
血液学
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产品关联
DOI
高影响因子
ACTA PHYSICO-CHIMICA SINICA
·
2025
·
IF 13.5
Chengxiao Zhao,Zhaolin Li,Dongfang Wu,Xiaofei Yang
Covalent triazine frameworks (CTFs) represent an attractive family of metal-free visible light-responsive covalent organic frameworks (COFs), possessing promising characteristics such as large specific surface area, rich nitrogen content, permanent porosity, and high thermal and chemical stability for photocatalytic hydrogen production via water splitting. Nevertheless, the majority of CTFs are confronted with difficulty in chemical synthesis and generally suffer from low electric conductivity and severe photogenerated charge carrier recombination during photocatalytic hydrogen evolution reaction (HER). The hydrogen-evolving performance highly depends on the structure of π-conjugated CTFs and the synthetic methods, and controlled synthesis of well-defined nanostructures is still highly challenging. In this work, we report the organic acid-catalyzed synthesis of porous CTF nanoarchitectures templated by mesoporous silica molecular sieve SBA-15 with a highly ordered hexagonal structure. The SBA-15 templated CTF-S2 nanorods exhibited a substantial increase in photocatalytic HER efficiency, with an impressive 14-fold enhancement compared to the micro-sized bulk CTF-1 (4.1 μmol h −1 ). This remarkable improvement in the photocatalytic HER over SBA-templated CTF-S2 nanostructure is attributed to the extended visible light absorption, accelerated charge carrier transfer and the optimized band structure.
研究领域:
材料科学
·
能源化学
·
纳米技术
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产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）