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SOLID STATE SCIENCES · 2018 · IF 1.861

Immobilization of trypsin onto large-pore mesoporous silica and optimization enzyme activity via response surface methodology

Jianyi Liu,Yan Liu,Dianxin Jin,Minjia Meng,Yinhua Jiang,Liang Ni,Zhanchao Liu

Tannic-acid-templated large pore mesoporous silica nanoparticle (LMSN) was synthesized using one-pot procedure and the external surface was further modified with APTES (LMSN-N) to immobilize trypsin. After modification, trypsin was difficult to be immobilized on the outer surface of the LMSN due to the electrostatic repulsion. Naturally, study of the trypsin immobilized in the interior pores could be implemented solely. Meanwhile, the activity of immobilized trypsin was optimized by response surface method (RSM), and the ANOVA was employed to explore the interaction between independent variables. The maximum enzyme activity (12.28 U/mg) was obtained under a certain condition that the quality of T-LMSN-N-272 was 153 μg, the pH was 7.9, and the temperature was 40.4 °C. Simultaneously, the immobilized enzyme was proved to possess better thermal stability, storage stability and recycling performance than free enzyme.

研究领域: 生物化学 · 材料科学 · 酶工程
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ELECTROCHIMICA ACTA · 2014 · IF 4.086

Nitrogen-containing mesoporous carbon cathode for lithium-oxygen batteries: The influence of Nitrogen on oxygen reduction reaction

Hongjiao Nie,Yining Zhang,Wei Zhou,Jing Li,Baoshan Wu,Tao Liu,Huamin Zhang

The direct effect of nitrogen content and various nitrogen species on oxygen reduction reaction (ORR) activities in non-aqueous lithium-oxygen (Li-O 2 ) batteries are systematically investigated. Mesoporous carbon (MC) with various nitrogen species is prepared through heat treatment of N-containing precursor under different temperature. The effect of the heat treatment temperature on the performance of carbon materials in Li-O 2 battery is investigated. The bonding state of nitrogen atoms is found to have a significant effect on the ORR activity. The ORR activity in Li-O 2 battery is proved to be dependent on the quaternary N content while the total N content in the carbon material does not play a crucial role in the ORR process.

研究领域: 电化学 · 能源材料 · 纳米材料 · 电催化 · 锂离子电池
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MATERIALS LETTERS · 2018 · IF 2.687

Synthesis of mesoporous hydroxyapatite via a vitamin C templating hydrothermal route

Huan Zhou,Ying Yang,Mengmeng Yang,Wenjie Wang,Yaping Bi

Mesoporous hydroxyapatite is widely applied in biomedical and environmental fields due to its high surface area and adsorption capacity. In current work a one-step hydrothermal method to synthesize mesoporous HA was developed with the assistance of a cost-effective template vitamin C. It was observed the pore size and morphology of hydrothermally synthesized HA were correlated to applied solution composition. A combination of calcium hydroxide, orthophosphate, and vitamin C can finally result in mesoporous rod-like HA nanoparticles with surface area of 88 m 2 .g −1 and pore size of 15.7 nm on average. The mesoporous HA exhibited enhanced adsorption of model drug doxorubicin in comparison to conventionally synthesized HA as expected. Consequently, this work provides new pathway to prepare mesoporous HA with advantages of economy and convenience.

研究领域: 生物材料学 · 纳米医学 · 药剂学 · 环境科学 · 生物无机化学
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MICROPOROUS AND MESOPOROUS MATERIALS · 2012 · IF 3.285

Structural and thermal stability of mesoporous alumina synthesized by Al-based coordination polymer

Yi Liu,Hai-Xiao He

Mesoporous alumina with a narrow pore size distribution is synthesized by direct thermolysis of Al-based coordination polymer. By applying the appropriate thermolysis temperature, both high surface area and large pore volume are obtained with the collapses and elimination of the 1,4-benzenedicarboxylate linkers of Al-based coordination polymer. This new class of mesoporous alumina display better adsorption properties and higher thermal stability, which retain mesoporous properties and high surface area after calcination in 900   °C. This thermolysis method provides a new approach to synthesize mesoporous alumina with high thermal stability by using coordination polymers.

研究领域: 材料科学 · 无机化学 · 纳米材料 · 多孔材料 · 热分析
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JOURNAL OF CHEMICAL AND ENGINEERING DATA · 2018 · IF 2.196

A Novel Amino and Carboxyl Functionalized Mesoporous Silica as an Efficient Adsorbent for Nickel(II)

Li Zhang,Fangxiang Song,Yonggui Wu,Liang Cheng,Jin Qian,Shuai Wang,Qianlin Chen,Yan Li

In this study, the as-prepared spherical mesoporous silica was modified by amino and cyano groups via grafting, and the amino and carboxyl functionalized adsorption materials (MSS@NH2@COOH) were obtained after cyano group hydrolysis. The introduction of amino and carboxyl groups increases the surface active sites of the materials. The materials were characterized by SEM, TEM, XRD, N2 adsorption/desorption, XPS, etc. BET analysis revealed the amino and carboxyl functionalized mesoporous silica maintained their mesostructure nature and its specific surface area was 113 m2·g–1. TG-DTA and FT-IR confirmed effective grafting on the surface of mesoporous silica with functionalized groups. The simulated wastewater of Ni(II) was carried out to test the adsorption properties of the materials, and several influential factors (pH, initial nickel ion concentration, adsorbent dose) were discussed. The saturated adsorption capacity increased clearly from 46.55 mg·g–1 of MSS to 125.57 mg·g–1 of MSS@NH2@COOH. Even recycling three times, the removal rate of Ni(II) ions using MSS@NH2@COOH as an adsorbent could still be over 75%. Adsorption isotherms, kinetics, and thermodynamics of adsorption were taken to clarify the adsorption process. This newly developed adsorbent material does exhibit good reusable performance and effective removal of the heavy metal ions of Ni(II).

CAS / MDL: 108-67-8
研究领域: 环境科学 · 材料科学
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INDUSTRIAL CROPS AND PRODUCTS · 2022 · IF 6.449

Eggplant biomass based porous carbon for fast and efficient dye adsorption from wastewater

Zhi Liu,Xiaohai Huang,Yi Miao,Bing Gao,Yiling Shi,Jianghui Zhao,Soon Huat Tan

Adsorption techniques have been successfully applied in water purification for their simplicity, efficiency, and negligible byproducts. Porous carbon materials are effective dye adsorbents but have relatively low adsorption efficiency, slow adsorption rate, and high production cost, all of which need to be addressed for conducive practical applications. Herein, natural eggplant-based porous carbon materials (EPCMs) have been studied and successfully constructed to perform with high efficiency and fast rate of removal of dyes from wastewater. The hierarchical pore structure and well-developed mesoporous had a total pore volume of 0.6379 cm 3 /g and a maximum specific surface area of 516.0060 m 2 /g, which contributed to the high efficiency of adsorption (100%). The complete adsorption of Rhodamine B (basic and cationic dyes) solution within 25 min demonstrated its fast and high adsorption performance. The EPCMs also showed its efficiency in the absorption of various dyes, including methyl orange (acidic and anionic dye), methylene blue (basic and cationic dyes), and Yuan’qing B (reactive dye). Furthermore, the EPCMs were tested with actual wastewater from a production-based factory and recorded excellent removal effects as well, suggesting its prospective expansion for industrial applications. Therefore, this eggplant biomass-based porous carbon provides a promising approach for fast and highly efficient wastewater purification from dye-based contaminations.

研究领域: 环境科学 · 材料科学 · 化学工程 · 环境污染治理 · 吸附技术
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Nano Energy · 2014 · IF 10.211

Hierarchical mesoporous Li2Mn0.5Fe0.5SiO4 and Li2Mn0.5Fe0.5SiO4/C assembled by nanoparticles or nanoplates as a cathode material for lithium-ion batteries

Xiaolei Jiang,Huayun Xu,Jing Liu,Jian Yang,Hongzhi Mao,Yitai Qian

Hierarchical mesoporous Li 2 Mn 0.5 Fe 0.5 SiO 4 consisted of nanoparticles or nanoplates has been successfully synthesized for the first time by a hydrothermal method . Their carbon-coated composites are obtained by a heat treatment in the presence of citric acid. These composites were characterized by powder X-ray diffractometry, scanning and transmission electron microscopy , Raman spectroscopy , and thermogravimetric analysis . The lithium storage capacity and cycling performance of the optimized Li 2 Mn 0.5 Fe 0.5 SiO 4 /C composite are greatly enhanced when tested as a cathode material in lithium-ion batteries (LIBs). It exhibits a discharge capacity of 125   mAh   g −1 after 60 cycles at a rate of 0.1   C. This superior electrochemical property could be ascribed to high purity and mesoporous structure of Li 2 Mn 0.5 Fe 0.5 SiO 4 , which greatly enhances the electronic conductivity as well as the diffusion coefficient of lithium ions .

研究领域: 材料科学 · 电化学 · 能源存储 · 纳米材料 · 固体化学
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DALTON TRANSACTIONS · 2012 ·Vol. 41 ·期 28 ·8567-8574 · IF 3.838

Luminescent hybrid materials of lanthanide β-diketonate and mesoporous host through covalent and ionic bonding with anion metathesis

Qiu-Ping Li,Bing Yan

Luminescent mesoporous materials were prepared by performing an anion metathesis reaction on ionic liquid modified SBA15, which has imidazolium chloride bridging units. The lanthanide β-diketonate complex anion was successfully anchored onto the SBA15 framework after the anion metathesis reaction. The resulting materials were characterized by FTIR, TEM, TGA, small-angle X-ray powder diffraction (SAXRD) and nitrogen adsorption–desorption isotherms. The photoluminescent properties of these materials were investigated in detail, and the results reveal that these hybrid mesoporous SBA15, prepared through this preparation approach, present favorable photoluminescent behavior such as high luminescent quantum efficiencies and long luminescent lifetimes.

研究领域: 材料化学 · 无机化学 · 光功能材料 · 纳米材料科学
✓ 已验证 DOI 高影响因子
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SENSORS AND ACTUATORS B-CHEMICAL · 2016 · IF 4.758

Mesoporous silica-deoxycholate synergistic substrate, a novel room temperature phosphorescence-sensing platform

Jun Qin,Xiaomei Li,Yunfeng Bai,Feng Feng,Qiliang Pan,Jianguo Zhao

A novel mesoporous silica-deoxycholate (MS-NaDC) synergistic substrate was developed for room-temperature phosphorescence (RTP) sensing and analysis. The substrate exhibited rapid and strong RTP-inducing ability toward 9-bromophenanthrene (9-BrP). The formation mechanism of MS-NaDC synergistic substrate was analyzed and demonstrated. Five MSs with pore size range of 2.73–18.58   nm were synthesized and investigated, and the MS designated as LPMS2 was selected for its rapid RTP protection and good stability in dispersions. RTP in the presence of MS-NaDC substrate also shows good thermostability. Assistant inducers, such as cyclohexane, can be used together for further RTP enhancement. Finally, 9-BrP holds a fairly wide linear concentration range of 2   nM–3   μM, and a detection limit of 0.5   nM. All the results demonstrated the feasibility and application potential of the MS-NaDC substrate in RTP.

研究领域: 分析化学 · 材料科学 · 生物传感器 · 纳米医学 · 分子探针 · 环境监测
✓ 已验证 DOI 高影响因子
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CHINESE JOURNAL OF POLYMER SCIENCE · 2015 ·Vol. 33 ·期 7 ·976-987 · IF 1.835

Enhanced ultraviolet resistance of polypropylene random copolymer filled by ZnO-supported mesoporous zeolite

Li Mei,Li Gu,Zhang Zi-shou,Dai Xin,Yang Yue-wen,Mai Kan-cheng

To enhance the ultraviolet resistance of ZnO based polymer materials, ZnO-supported mesoporous zeolite (M-ZnO) was prepared and characterized by atomic absorption spectroscopy and scanning electron microscopy. The ultraviolet resistance, crystallization behavior and melting characteristics of ZnO and M-ZnO filled PPR composites were compared by FTIR spectra and differential scanning calorimetry. The ultraviolet resistance of M-ZnO filled PPR composites is higher than that of ZnO filled PPR composites, indicating higher ultraviolet resistance of M-ZnO than that of ZnO. The crystallization temperatures of mesoporous zeolite filled PPR were higher than those of M-ZnO and decreased with increasing UV-irradiation time. But the crystallization temperatures of M-ZnO filled PPR composites were not influenced by UV-irradiation time. The ZnO supported on the surface of zeolite is effective in enhancing the ultraviolet resistance of ZnO based polymer materials.

研究领域: 高分子材料科学 · 功能复合材料 · 材料老化与稳定性 · 纳米复合材料 · 聚合物改性
✓ 已验证 DOI 高影响因子
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MATERIALS LETTERS · 2013 · IF 2.224

Synthesis of fibrous monodisperse core–shell Fe3O4/SiO2/KCC-1

Kejie Yu,Xuebin Zhang,Hongwu Tong,Xiangyan Yan,Shaomin Liu

Fibrous monodisperse core–shell structured Fe 3 O 4 /SiO 2 /KCC-1 nanoparticles were synthesised successfully through a surfactant-templated microemulsion formation process. The structure and morphology of the synthesised nanoparticles were investigated by scanning electron microscopy , transmission electron microscopy , superconducting quantum interference device susceptometer, X-ray diffraction, thermogravimetric analysis and N 2 adsorption/desorption. These nanoparticles showed monodisperse spherical morphology, high magnetism , good thermal stability , large surface area , direct channels, easily accessible large pores and narrow size distribution. A mechanism for the synthesis of these nanoparticles was proposed and explained. Adsorption experiments indicated that the as-prepared materials had good adsorption capacity for dye and could perform a fast transfer of molecules, indicating its promising application in purification of industrial wastewater, drug delivery and so on.

研究领域: 纳米医学 · 材料科学 · 环境工程 · 生物材料 · 药剂学 · 胶体与界面化学
✓ 已验证 DOI 高影响因子
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2016 ·Vol. 41 ·期 39 ·17462-17470 · IF 3.205

Enhanced hydrogen desorption properties of LiBH4–Ca(BH4)2 by a synergetic effect of nanoconfinement and catalysis

Bing Zhai,Xuezhang Xiao,Wenping Lin,Xu Huang,Xiulin Fan,Shouquan Li,Hongwei Ge,Qidong Wang,Lixin Chen

NbF 5 and eutectic 0.68LiBH 4 –0.32Ca(BH 4 ) 2 were successively infiltrated into highly ordered mesoporous carbon (CMK-3) to obtain a LiBH 4 –Ca(BH 4 ) 2 –NbF 5 @CMK-3 composite. A synergetic effect of nanoconfinement and catalysis on hydrogen desorption properties of the composite was achieved. The onset desorption temperature of LiBH 4 –Ca(BH 4 ) 2 –NbF 5 @CMK-3 is dramatically lower than 120 °C compared with that of as-milled LiBH 4 –Ca(BH 4 ) 2 or LiBH 4 –Ca(BH 4 ) 2 @CMK-3. A hydrogen amount as high as 13.3 wt% can be released within 250 min for LiBH 4 –Ca(BH 4 ) 2 –NbF 5 @CMK-3, compared with only 10.4 wt% for pure LiBH 4 –Ca(BH 4 ) 2 , in which nanoconfinement and catalysis both make some contribution. The cycling hydrogen desorption performance of the composite becomes better likewise due to the addition of NbF 5 . Further microstructure analysis reveals that F − tended to bind with Ca 2+ to form CaF 2 , whereas Nb compound is believed to catalyze the whole system in the form of Nb-based boride (NbB 2 ).

研究领域: 材料科学 · 能源化学 · 纳米科技 · 储氢材料 · 物理化学
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