COLLOID AND POLYMER SCIENCE
·
2014
·Vol. 293
·期 1
·109-123
·
IF 2.41
Liu Yan,Chen Rui,Yuan Dandan,Liu Zhanchao,Meng Minjia,Wang Yun,Han Juan,Meng Xiangguo,Liu Fangfang,Hu Zhaoyong,Guo Wenlu,Ni Liang,Yan Yongsheng
Highly thermal-responsive magnetic Sr(II)-imprinted polymer (Sr(II)-TMIIP) was successfully synthesized as a potential effective adsorbent for selective removal of Sr(II) in aquatic environments. First, magnetic polyethyleneimine-loaded mesoporous SBA-15 (Fe 3 O 4 @PEI-SBA-15) was prepared via a simple polymer-mediated self-assembly method. Then, the surface of Fe 3 O 4 @PEI-SBA-15 was endowed with reactive vinyl groups through modification with 3-(methacryloyloxy)propyl trimethoxysilane (MPS). With the aid of vinyl groups, free radical polymerization of N -isopropylacrylamide (NIPAM), methacrylic acid (MAA), and N , N ′-methylenebisacrylamide (BIS) in the presence of Sr(II) was performed with 2,2′-azobisisobutyronitrile (AIBN) as initiator, which provided a desired imprinted layer coating onto Fe 3 O 4 @PEI-SBA-15. The as-prepared Sr(II)-TMIIP was characterized by Fourier transmission infrared spectra (FT-IR), X-ray diffractometer (XRD), thermogravimetric analysis (TGA), scanning electron microscope (SEM), transmission electron microscope (TEM), vibrating sample magnetometer (VSM), UV, and N 2 adsorption–desorption techniques. The results showed that the Sr(II)-TMIIP exhibited thermal stability, temperature and magnetic sensitivity ( M
s = 10.34 emu/g), and ordered mesoporous structure. Batch mode adsorption studies were conducted to investigate the specific binding kinetics, adsorption equilibrium, and selective recognition ability of Sr(II)-TMIIP. Adsorption equilibrium experiments showed that the adsorption amount strongly depended on temperature and reached a maximum around the lower critical solution temperature (LCST). Regeneration experiments indicated that repeated adsorption and desorption by temperature swings were possible. Compared with the nonimprinted polymer (NIP), the Sr(II)-TMIIP had good temperature response and excellent selectivity and reusability, making it possible in applying for Sr(II) separation and controlled release.
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ACS Applied Materials & Interfaces
·
2025
·
IF 8.2
Xiao Dan Sun,Zhangxin Duan,Jingjing Song,Hanxing Yang,Kai Yan,Zhenhua Tian,Dangge Gao,Jianzhong Ma
Carcinogen Cr(VI) is reduced efficiently into Cr(III) by a photocatalyst, but the produced Cr(III) is difficult to transfer from the photocatalytic active site. The “two birds with one stone” strategy is proposed to realize the in situ growth of ZnIn2S4 nanoplates on SBA-15 and the creation of separated active sites, in which ZnO loading on the porous SBA-15 nanorod was used as a zinc source. Obtained samples ZnIn2S4/SBA-15 (ZIS/SBA) showed the redshift of the absorption band and better separation of photoinduced carriers than pristine ZnIn2S4, due to its smaller size and S defect. All of the Cr(VI) was reduced to Cr(III) by the ZIS/SBA sample during the photocatalytic process, which was 2 times higher than pristine ZnIn2S4. Moreover, 92.8% of Cr(III) was adsorbed simultaneously during photocatalysis due to the electrostatic interaction from SBA-15. In addition, the ZIS/SBA sample showed good recycling stability after 5 times cycles, providing a new strategy for the in situ growth of ZnIn2S4 on the surface of porous materials and a novel way for the simultaneous removal of Cr(VI) and Cr(III) during photocatalysis.
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INDUSTRIAL CROPS AND PRODUCTS
·
2025
·
IF 6.2
Siyu Zhou,Wanni Liu,Dongqi Liu,Xian Shi,Kai Huang,Feng Jiang,Hui Gao,Haian Xia,Ying Guan,Siquan Xu
Efficient catalytic conversion of cellulose into 5-hydroxymethylfurfural (HMF) remains challenging and arouses concern. In this study, iron phosphate (FePO 4 ) was embedded into the SBA-15 mesoporous silica matrix as an available active phase via ultrasound-assisted implantation, and then the abundant silanol nests were utilized to graft sulfonic acid groups to construct an innovative FeP@SBA-15-S catalyst. Through a systematic analysis of the characteristics of crystal, texture, element valence, acidity, hydrophilicity, etc., it was reflected that FeP@SBA-15-S catalyst gave the active FePO 4 component porosity and exhibited bifunctional acidity. Without pretreatment and other acid additives, FeP@SBA-15-S catalyzed cellulose under optimal conditions provided a desired HMF yield of 52 %. More meaningfully, the cellulose and hemicellulose components in native wheat straw could be catalyzed simultaneously by FeP@SBA-15-S catalyst, yielding 61 % HMF and 60 % furfural in one-pot. The cyclability evaluation showed that the FeP@SBA-15-S catalyst still had considerable activity after six continuous runs, with a slight loss in activity attributed to the leaching of active components and pore coverage. A clear catalytic pathway was summarized by GC-MS and 13 C NMR spectrum as cellulose undergoing glucose monomer ring opening, isomerization to fructose, fructose ring closure and final dehydration, and the by-products were also detected as mainly C 3 -C 23 fragments and oligomers.
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ACS Sustainable Chemistry & Engineering
·
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.
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FUEL
·
2023
·
IF 7.4
Yibo Zhang,Wei Wang,Chunlai Liu,Peihang Shen,Zelong Liu,Jianglei Hu,Fengwei Shi
In this work, we successfully synthesized a novel composite (HPW@MOF-199/SBA-15C, PMS-15C) in which MOF-199 encapsulated HPW catalyst (named HPW@MOF-199) was confined in SBA-15C, which is the carboxy-functionalized SBA-15. Physicochemical properties of the composites PMS-15C were systemically characterized by N 2 adsorption–desorption isotherms, wide-angle and low-angle XRD, XPS, FT-IR, SEM, and TEM. The results exhibited that HPW@MOF-199 had been successfully synthesized and embedded into the SBA-15C pores by COOH on the surface of SBA-15C. Meanwhile, the composites PMS-15C exhibited high activity and excellent reuse properties in the esterification reaction of acetic acid and ethanol, and no evidence of aggregation, leaching, or inactivation of HPW@MOF-199 during repeated use. The good dispersion of HPW within the MOF-199 cage and the interaction between HPW@MOF-199 and SBA-15C may be responsible for the good catalytic activity as well as the high stability of PMS-15C.
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JOURNAL OF APPLIED PHYSICS
·
2020
·Vol. 127
·期 11
·
IF 2.286
Xu Xiang,Zou Yu,He Junjie,Zeng Yanning,Yu Caili,Zhang Faai
Mesoporous silica nanoparticles/polymer hybrid materials were prepared via metal-free surface-initiated atom-transfer radical polymerization (SI-ATRP). Self-synthesized mesoporous SBA-15 with surface hydroxyl groups was modified with (3-aminopropyl)-triethoxysilane, followed by anchoring of the ATRP initiator α-bromoisobutyryl bromide onto the surface via amide reaction. The SI-ATRP of methyl methacrylate was then carried out with fluorescein (FL) as a photocatalyst and trimethylamine (TEA) as an electron donor under irradiation with blue light. Thus, polymer chains grew directly from mesoporous walls. The hybrid materials were characterized by gel permeation chromatography, N 2 adsorption/desorption measurements, and thermogravimetric analysis. The effects of the ligand/photocatalyst molar ratios, solvent, and the monomer/initiator molar ratios on grafting density, molecular weight, and molecular-weight distribution were investigated. The results show that a higher TEA/FL ratio led to a higher reaction rate and better controllability of the polymerization but also to a lower grafting density. These properties were also affected by the solvent. With an increasing monomer/initiator molar ratio, the grafting rate, molecular weight, and grafting density exhibited increasing trends.
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ACS Sustainable Chemistry & Engineering
·
2020
·
IF 7.632
Junhua Zhang,Yao Liu,Shibo Yang,Junnan Wei,Liang He,Lincai Peng,Xing Tang,Yonghao Ni
Biorefinery for the purpose of producing biofuels, chemicals, and materials has received much attention. Furfural alcohol (FOL) and levulinate ester (LE) are important biomass-derived platform chemicals, and they are produced from sugar-based furfural (FAL). Unfortunately, the two products are often obtained separately in different reaction systems, which is undesirable; furthermore, it is of significant practical interest to control their selectivity so that the desired product can be accumulated in high yields. Herein, we present an efficient method for the highly selective conversion of FAL to FOL or isopropyl levulinate (IPL) in a one pot system using isopropanol as the hydrogen source and ZrO2@SBA-15 as a bifunctional catalyst with both Lewis acid and Brønsted acid sites. Under optimized reaction conditions, high yields of FOL and IPL in up to 90.4% and 87.2%, respectively, were obtained. Based on the experimental results, a kinetic model describing the catalytic conversion of FAL into FOL and IPL process has been established, which has a good correlation (R2 > 0.92) between the measured and predicted data. The developed kinetics can provide an effective tool to monitor the process and tailor the process conditions to obtain the desired product.
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JOURNAL OF CATALYSIS
·
2020
·
IF 7.888
Jichang Lu,Jian Fang,Zhizhi Xu,Dedong He,Siyou Feng,Yubei Li,Gengping Wan,Sufang He,Hua Wu,Yongming Luo
Supported MoS 2 based materials are widely used as heterogeneous catalysts. In this work, we propose a rapid and facile method (ultrasound-induced impregnation assisted by microwave thermal treatment) to synthesize mesoporous silica (SBA-15)-supported, few-layer, ordered and K-promoted MoS 2 nanosheets with different K/Mo ratios. The prepared catalysts are characterized by various physical and chemical techniques. Their catalytic performance is evaluated by methyl mercaptan (CH 3 SH) synthesis from CO/H 2 /H 2 S. The results show that our catalysts exhibit a much higher CO conversion and selectivity to CH 3 SH than the catalysts prepared using the conventional impregnation and reported in the literature. The good performance arises because of two main factors: MoS 2 nanosheets of only 2–4 layers and K promotion. Experimental characterizations and (density functional theory) calculations show that the former is the typical nano-size effect, and the latter stabilizes C S bonds when activating COS molecules.
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INTERNATIONAL JOURNAL OF ENERGY RESEARCH
·
2020
·Vol. 44
·期 14
·11564-11582
·
IF 3.741
Wei Liu,Hong Yuan
Summary Hydrogen is considered an ideal energy carrier. However, the use of fossil fuels to produce hydrogen depletes natural resources and causes environmental problems. Therefore, there is an urgent need to find alternative raw materials and technologies for the production of hydrogen. Waste cooking oil (WCO) is a renewable energy source that has emerged as a potential raw material for hydrogen production. This study describes the production of hydrogen and carbon nanotubes (CNTs) by catalytic cracking of a WCO model compound (WCOMC) performed in a lab-scale fixed bed using Ni-Co/SBA-15 catalysts. The phase, structure and reduction properties of the catalyst were analysed by using different characterisation methods. The effects of the nickel-cobalt metal content and the reaction temperature on both the hydrogen production and the quality of the CNTs were investigated. The deposited carbonaceous products were characterised to analyse their external appearance, internal structure, oxidation stability and graphitisation degree. The results indicated that the catalyst containing 20% Ni and 30% Co showed the highest activity. When reaction temperature was 800°C, the instantaneous volume fraction of hydrogen was close to 43.5 vol% and the content of hydrogen in the gas product was close to 66.5 vol%. A few multi-walled CNTs having a small diameter and some CNTs with an open-topped structure were deposited on 10%Ni-40%Co/SBA-15 and 30%Ni-20%Co/SBA-15, respectively. Thermogravimetric analysis and Raman spectroscopic analysis indicated that all CNTs showed high oxidation stability and a high degree of graphitisation.
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JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY
·
2018
·Vol. 93
·期 10
·3028-3034
·
IF 2.587
Wei Chen,Yong Sun,Juan Du,Zhihao Si,Xing Tang,Xianhai Zeng,Lu Lin,Shijie Liu,Tingzhou Lei
BACKGROUND 5-(Aminomethyl)-2-furanmethanol (AMF), used widely in medicinal chemistry, is usually synthesized by the reductive amination of furfural or 5-hydroxymethylfurfural (HMF) with ammonia. However, a challenging task when synthesizing this furyl primary amine is to enhance the selectivity of the product due to its high nucleophilicity. Conventional measures have used excessive liquid ammonia and precious metal catalysts. Usually, the molar ratio of ammonia to substrate is up to 30:1. This study employed aqueous ammonia to synthesize AMF by the direct reductive amination of HMF using the non-noble metal Ni/SBA-15 catalyst. RESULTS The Ni/SBA-15 catalyst displayed higher catalytic selectivity in the reductive amination of HMF to AMF compared to other precious metal catalysts, such as Ru/C, Pd/C and Pt/C. The AMF yield of 89.8% was obtained at the relatively mild reaction temperature of 100 °C for 4 h. After the fifth cycle, an acceptable decrease in catalytic activity with 74.2% yield of AMF was observed. CONCLUSION An improved process was developed for preparing AMF by the reductive amination of HMF with aqueous ammonia using the non-noble Ni/SBA-15 catalyst. The high selectivity of nickel catalyst is attributed mainly to the moderate catalytic activity. Moreover, a small amount of water enhanced the yield of AMF by promoting the formation of ammonium ions to prevent the further side reaction of AMF with HMF. Results of recycling experiments and analyses showed that agglomeration, loss and oxidization of nickel species together with carbon deposition were responsible for the slight deactivation of the catalyst. © 2018 Society of Chemical Industry
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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.
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FOOD CHEMISTRY
·
2017
·
IF 4.529
Hongwu Wang,Yanqing Liu,Su Yao,Peijie Zhu
In this work, a highly selective molecular imprinted polymer (SBA-15@MIP) was prepared using dicyandiamide (DCD) as the template molecule and mesoporous silica SBA-15 as the carrier. The resulting polymers were characterized by scanning electron microscopy and FT-IR spectra. A highly ordered mesoporous nanostructure was observed for the fabricated polymer. The performance tests showed that the adsorption capacity of SBA-15@MIP for DCD was higher than those of non-imprinted mesoporous silica polymer (SBA-15@NIP) and SBA-15. SBA-15@MIP was successfully used as the solid-phase extraction (SPE) sorbent coupled with HPLC for trace DCD determination in bovine milk and milk powder. Under selected conditions, a favorable linearity between 1 μg/mL and 100 μg/mL was obtained and the detection limit was estimated to be 0.08 μg/mL (bovine milk) and 0.10 μg/mL (milk powder). These results indicated that SBA-15@MIP could be used as an efficient SPE adsorbent for enrichment of DCD in bovine milk and milk powder.
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