FUEL
·
2022
·
IF 8.035
Puxiang Yan,Haiyong Wang,Yuhe Liao,Pengyao Sun,Chenguang Wang
Catalytic valorization of biomass into chemicals and fuels plays a key role in order to achieve net-zero greenhouse gas emissions. Herein, a series of hierarchical ZSM-5 zeolites were synthesized by the post-treatment method to transform furfural alcohol (FAL) to levulinic acid (LA). ZSM-5 obtained from tandem alkaline treatment (0.2 M NaOH) and acid washing (0.1 M HCl), denoted as ZSM-5-OH 0.2 -H, exhibited the highest activity, affording 76.2% LA yield in 9:1 acetone–water mixed solvents at 393 K for 0.5 h. The enhanced adsorption capacity and acid accessibility of FAL on zeolite mediated by the introduction of mesopores, as well as the reduced secondary reactions of the generated LA due to few Al atoms in straight and sinusoidal channels (as confirmed by UV–vis diffuse reflectance), were responsible for the outstanding catalytic performance of ZSM-5-OH 0.2 -H. The structure–activity relationship revealed that regulating the porous structure and Al distribution of ZSM-5 was an effective strategy to enhance its hydrolytic performance of FAL to LA. Moreover, ZSM-5-OH 0.2 -H could be reused for three reaction cycles without significant loss in catalytic activity.
研究领域:
化学工程
·
催化
·
生物质转化
·
可持续化学
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DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2019
·
IF 8.355
Fang Guo,Ping Xiao,Bingyi Yan,Misun Hahn,Yuyu Kong,Wang Zhang,Yuanzhe Piao,Guowang Diao
A novel and simple strategy for one-pot preparation of supramolecular reduced graphene oxide (RGO) hybrid material based on pillar[5]arenes was developed by the redox reaction between graphene oxide (GO) and hydrazide-pillar[5]arene (HP5A, as the reducing agent and stabilizer) in aqueous solution. In this process, no additional reducing agents needed to be added, and no extra modification steps were required after reducing GO. The few-layer RGO-HP5A hybrids fabricated could be dispersed in the water easily and stably. When applied to supercapacitors, this nanocomposite showed a remarkable specific capacitance (331 F·g −1 at 0.5 A·g −1 ) and great rate capability in the three-electrode cell, which benefited from synergistic effect of RGO and HP5A in this nanocomposite. Moreover, the as-prepared symmetric supercapacitor with RGO-HP5A exhibited a high initial capacitance as well as an excellent cycling stability. Thus, the study provided a feasible electrode component for fabrication of supercapacitors with outstanding performance and a potential tool for expanding the development of supramolecular composite in energy storage.
研究领域:
材料科学
·
纳米科技
·
电化学
·
能源存储
·
高分子化学
·
界面化学
✓ 已验证
DOI
高影响因子
CATALYSIS SURVEYS FROM ASIA
·
2025
·
IF 2.3
Zhu Mengxuan,Li Hongqing,Wang Xin,Wang Longyang,Wang Rui,Jiang Heng,Jin Changzi
Design of efficient metal-acid bifunction catalysts is of significance for development of hydroisomerization of linear alkanes. In this study, the spatial configurational construction of Pt-ZSM-5 catalytic system was achieved by fabrication of acidic ZSM-5 zeolite and mesoporous silica core-shell composites equipped with controlled location of Pt sites, which aim to explore the effect of functional sites proximity on isomerization reactivity. A series of characterization techniques such as X-ray diffraction, transmission electronic microscopy, N 2 physical adsorption, NH 3 temperature programmed desorption, X-ray photoelectron spectroscopy and so on had confirmed that the synthesized core-shell bifunctional catalysts with different Pt location possessing similar textural, acid and metal properties. In the catalytic hydroisomerization of n -heptane, however, the catalyst with Pt sites locating at acid zeolite exhibits superior n -heptane conversion and isomerization selectivity, which indicates that proximity of active sites at atomic scale may be more conducive to their synergistic effect when the diffusional limitation from zeolitic channel is minimized. These results had presented new direction for the preparation of efficient bifunctional catalysts in hydroisomerization of linear alkanes.
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产品关联
DOI
高影响因子
JOURNAL OF SEPARATION SCIENCE
·
2015
·Vol. 38
·期 14
·2387-2393
·
IF 2.737
Jun Yan,Qi-Lei Zhang,Hong-Fei Tong,Dong-Qiang Lin,Shan-Jing Yao
A new hydrophobic charge-induction chromatography resin was prepared with 5-aminobenzimidazol as functional ligand and polyacrylic ester beads as matrix. Adsorption isotherms and adsorption in columns were investigated using human immunoglobulin G and bovine serum albumin as model proteins, and the influence of pH and NaCl concentration was discussed. Results showed that the ligand density was 195 μmol/mL gel, and protein selectivity can be improved by controlling pH and salt addition. An optimized purification process (sample loading at pH 8.0 with 0.2 M NaCl and elution at pH 5.0) was performed to purify human immunoglobulin G from bovine serum albumin containing feedstock, which resulted in human immunoglobulin G purity of 99.7% and recovery of 94.6%. A similar process was applied for the purification of monoclonal antibody from cell culture supernatant, which showed antibody purity of 94.9% and recovery of 92.5%. The results indicated that the new resin developed had comparable performance as Protein A chromatography and would be suitable for antibody purification from complex feedstock.
研究领域:
生物化学
·
蛋白质纯化
·
生物工程
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产品关联
DOI
PubMed
高影响因子
CRYSTENGCOMM
·
2018
·Vol. 20
·期 40
·6319-6327
·
IF 3.304
Yu Shen,Zongzhuang Han,Hang Li,Haichao Li,Gang Wang,Fumin Wang,Xubin Zhang
Hierarchical ZSM-5 zeolite with short-range ordered mesoporosity and hierarchical ZSM-5 zeolite nanorods were obtained via a direct hydrothermal synthesis by the cooperative structure direction of dimethyloctadecyl[3-(trimethoxysilyl)propyl]- ammonium chloride (TPOAC) and tetrapropylammonium hydroxide (TPAOH). Dimethyloctadecyl[3-(dimethoxymethylsilyl)propyl]ammonium chloride (DPOAC) and octadecyltrimethylammonium chloride (OTAC) were also employed as structure directing agents (SDA) to further explore the role of methoxysilyl groups in organosilanes during the formation of hierarchical structure. The prepared materials were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), N2 adsorption–desorption, FT-IR, UV-vis and inductively coupled plasma-optical emission spectroscopy (ICP-OES). The characterization results showed that the use of TPOAC and DPOAC would generate short-range ordered mesopores and irregular mesopores, respectively. Hierarchical ZSM-5 zeolite nanorods with worm-like intracrystalline mesopores could be obtained by adjusting the amount of silicon source. The lack of methoxysilyl groups in OTAC however could lead to phase separation problems. Furthermore, the hierarchical Fe-ZSM-5 zeolite with short-range ordered mesoporosity showed enhanced catalytic activity and stability for the hydroxylation of phenol at room temperature.
研究领域:
材料科学
·
催化化学
✓ 已验证
DOI
高影响因子
Journal of Environmental Chemical Engineering
·
2025
·
IF 7.2
Xu Yue,Sheng Wang,Shudong Wang
ZSM-5 zeolite adsorbents exhibit limited adsorption capacity for volatile organic compounds (VOCs) under high-humidity conditions, constraining their industrial applicability. In this study, a series of hierarchical ZSM-5 zeolites with high silica-to-alumina ratios (SARs) were successfully prepared via a facile acid pretreatment followed by surface methyl grafting. Using toluene as a representative VOC, the adsorption and desorption properties of these samples were assessed through dynamic adsorption breakthrough curves and temperature-programmed desorption (TPD) experiments. It was found that the two-step modification significantly enhanced both the breakthrough time and saturation adsorption capacity of high-SAR ZSM-5 for toluene in the presence of water vapor. AHFS-TZ5 and HCl-TZ5 exhibited superior performance, showing 53.9 % and 59.5 % enhancements in breakthrough time over ZSM-5, respectively. Specifically, the toluene adsorption capacity of AHFS-TZ5 under humid conditions (4 vol% H 2 O) reached 67.38 mg·g −1 , approximately 1.47 times higher than that of the unmodified ZSM-5. However, the hydrophobic -CH 3 groups grafted onto the ZSM-5 surface moderately hindered toluene diffusion due to increased steric hindrance. Additionally, AHFS-TZ5 exhibited excellent regeneration ability after desorption at 180 ºC, retaining 95 % of its initial adsorption capacity. This study provided a promising approach for preparing hydrophobic zeolites, offering a potential solution for efficient VOC adsorption in high-humidity flue gas environments.
研究领域:
环境科学
·
材料化学
·
吸附分离
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大气污染控制
·
多孔材料
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产品关联
DOI
高影响因子
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2023
·
IF 4.2
Xuemin Cao,Kun Zhang,Yu Wang,Peng He
The carbonylation of formaldehyde offers a promising, cost-effective, and environmentally friendly method for synthesizing glycolic acid, a crucial monomer in biodegradable plastics. This study highlights the development and optimization of a bifunctional PdO/ZSM-5 zeolite catalyst for this process. Investigations via various spectroscopic techniques reveal that Pd species, predominantly in the form of PdO, enhance the CO activation, thereby boosting the formaldehyde carbonylation reaction rate significantly. The optimal catalytic performance was observed with a Pd-loading of 2 wt %. Notably, excessive Pd loading was found to impede the catalytic performance by overoccupying acid sites, thereby reducing its capacity to activate formaldehyde. The concurrent activation of formaldehyde and CO at the Brønsted acid site and the PdO site, respectively, through a Langmuir–Hinshelwood mechanism is key to the enhanced catalytic performance. These findings underscore the importance of CO activation in improving the formaldehyde carbonylation process, offering vital insights for catalyst optimization.
研究领域:
催化化学
·
化学合成
·
环境化学
·
高分子科学
✓ 已验证
DOI
高影响因子
JOURNAL OF CHEMICAL RESEARCH
·
2016
·
IF 0.661
Hui-Long Zhu,Yu-Wei Liu,Wei-Wei Liu,Fu-Jun Yin,Zhi-Ling Cao,Juan Bao,Meng Li,Ling-Yan Qin,Da-Hua Shi
Four 5-benzyl-1,3,4-thiadiazol-2-amine derivatives were synthesised from phenylacetic acid derivatives. The structures of the 5-benzyl-1,3,4-thiadiazole derivatives were characterised by NMR spectroscopy and X-ray crystallography. The acetylcholinesterase-inhibition activities were also tested. Among the four compounds, 5- (4-bromobenzyl)-1,3,4-thiadiazol-2-amine showed the best acetylcholinesterase-inhibition activity with an IC50 of 49.86 μM. The docking study performed with AUTODOCK demonstrated that this compound could interact with the catalytic active site of acetylcholinesterase.
研究领域:
药物化学
·
生物化学
·
结构生物学
✓ 已验证
DOI
高影响因子
ChemSusChem
·
2022
·Vol. 15
·期 13
·e202200233
·
IF 9.14
Zuojun Wei,Yuran Cheng,Hao Huang,Zhihe Ma,Kuo Zhou,Yingxin Liu
Graphical Simply the best : 14 Secondary metals and 6 catalytic supports are screened to fabricated Ni-based 10NiMn(4 : 1)/γ-Al 2 O 3 catalyst with improved activity and stability for the reductive amination of 5-hydroxymethylfurfural to 2,5-bis(aminomethyl)furan, which is attributed to the electron transfer effect between active Ni particles and the well-dispersed MnO x on the γ-Al 2 O 3 support. Mono- and bimetallic Ni-based catalysts were prepared by screening 6 supports and 14 secondary metals for reductive amination of 5-hydroxymethylfurfural (5-HMF) into 2,5-bis(aminomethyl)furan (BAMF), among which γ-Al 2 O 3 and Mn were the best candidates. By further optimization of the reaction conditions at 0.4 g catalyst loading for 0.5 g substrate of 5-HMF and 160 °C of reaction temperature, 10Ni/γ-Al 2 O 3 and 10NiMn(4 : 1)/γ-Al 2 O 3 achieved the highest BAMF yields of 86.3 and 82.1 %, respectively. Although the BAMF yield values were comparable with that over Raney Ni, the turnover frequencies based on the initial BAMF yield and unit weight of Ni for 10NiMn(4 : 1)/γ-Al 2 O 3 , 10Ni/γ-Al 2 O 3 , and Raney Ni were calculated as 0.41, 0.09, and 0.04 h −1 , respectively. X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy showed that the existence of MnO x well dispersed on the γ-Al 2 O 3 support and its electron transfer effect with Ni particles on the surface of the support contributed to the high efficiency and better recyclability for the five-time reused 10NiMn(4 : 1)/γ-Al 2 O 3 catalyst.
研究领域:
催化化学
·
材料科学
✓ 已验证
DOI
PubMed
高影响因子
ACS Sustainable Chemistry & Engineering
·
2022
·
IF 9.224
Yafei Li,Shiqing Wang,Shunxin Fan,Babar Ali,Xiaocheng Lan,Tiefeng Wang
For the ethanolysis of biomass-derived furfuryl alcohol (FA) to value-added ethyl levulinate (EL), the development of an efficient solid acid catalyst is very important for industrial application with high FA concentration. Herein, a H-ZSM-5 catalyst with nano b-axis channels (NB-H-ZSM-5) was synthesized and used for the conversion of FA. Detailed catalyst characterization proved that the NB-H-ZSM-5 catalysts (Si/Al = 25∼125) with ∼70 nm b-axis channels were successfully prepared. The NB-H-ZSM-5 catalyst with Si/Al = 75 showed the highest activity. Its structural characteristics allowed for fast diffusion of reactants and products and full utilization of active sites, which endowed it with higher activity compared to commercial H-ZSM-5 (C-H-ZSM-5). Its moderate acidity effectively inhibited the polymerization of FA even at a high FA concentration of 20 wt %. The spent catalyst was easily regenerated by coke burn-off to give a good recyclability. Furthermore, based on the proposed reaction network, a method of physically mixing the NB-H-ZSM-5 (75) catalyst with a small amount of Amberlyst-15 was proposed to further increase the EL yield from 64.7 to 82.1% at an FA concentration of 6 wt %.
研究领域:
催化化学
·
可再生资源化学
·
材料科学
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DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2020
·
IF 9.038
Yimin Cai,Seraj A. Ansari,Kuirong Fu,Beichen Zhu,Haoyang Ma,Lixi Chen,Steven D. Conradson,Song Qin,Haiying Fu,Prasanta K. Mohapatra,Lihua Yuan,Wen Feng
Selective extraction of highly radiotoxic actinides(III) is an important and challenging task in nuclear wastewater treatment . Many proposed ligands containing S or P atoms have drawbacks including high reagent consumption and possible secondary pollution after incineration. The present work reports five novel pillar[5]arene-based extractants that are anchored with picolinamide substituents of different electronic nature by varying spacer. These ligands reveal highly efficient separation of actinides(III) over lanthanides(III). Specifically, almost all of these ligands could extract Am(III) over Eu(III) selectively at around pH 3.0 (SF Am/Eu > 11) with fast extraction kinetics. Variation of the pyridine nitrogen basicity via changing para-substitution leads to an increase in the distribution ratios by a factor of over 300 times for Am(III) with an electron-withdrawing group compared to those with an electron donating group. Investigation of complexation mechanism by slope analysis, NMR, IR, EXAFS , and DFT techniques indicates that each ligand binds two metal ions by pyridine nitrogen and amide oxygen. Finally, these ligands do not show obvious decrease in both extraction and separation ability after being exposed to 250 kGy absorbed gamma radiation . These results demonstrate the potential application of pillar[5]arene-picolinamides for actinide(III) separation.
研究领域:
化学
·
核废料处理
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产品关联
DOI
PubMed
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2025
·
IF 9.7
Hongke Li,Yunlei Zhang,Yiran Liu,Qinghua Xia,Maobin Wei,Wen Guan,Fang Wang,Yao Chen
Production of high value-added 2,5-furandicarboxylic acid (FDCA) from 5-hydroxymethylfurfural (HMF) is a promising alternative to petroleum derivate of terephthalic acid. However, it is still challenging to construct efficient and easily available catalysts suitable for green production process of FDCA under base-free conditions. Herein, a natural clay mineral sepiolite supported AuPd bimetallic catalysts with varied bimetallic ratio were developed and employed for aerobic oxidation of HMF to produce FDCA under alkali-free hydrothermal conditions. Au 1.2 Pd 1 /sepiolite catalyst showed the best catalytic performance with 100% HMF conversion and 98.4% FDCA yield. The key to excellent catalytic performance benefited from synergistic effect between hydroxy-rich surface property of natural sepiolite support and the positive role of AuPd bimetallic sites in the tandem oxidation of aldehyde and hydroxyl groups. The localized electron transfer between AuPd nanoparticles and carriers was investigated by density functional theory calculations. The bimetal promoted the formation of electron-rich interfaces, modulated the local electron redistribution at the interface, and enhanced the adsorption and activation of O 2 , HMF, and the reacted formed intermediates. This work presents a promising strategy for green synthesis of FDCA as well as offers a facile way for the high-value usage of nanofibrous clay mineral.
研究领域:
化学工程
·
材料科学
·
环境科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）