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FUEL · 2022 · IF 8.035

Introducing mesopore and regulating Al distribution for improving catalytic performances of ZSM-5 in furfuryl alcohol to levulinic acid

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
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2019 · IF 8.355

One-pot synthesis of hydrazide-pillar[5]arene functionalized reduced graphene oxide for supercapacitor electrode

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
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ACS Sustainable Chemistry & Engineering · 2022 · IF 9.224

Nano-H-ZSM-5 with Short b-Axis Channels as a Highly Efficient Catalyst for the Synthesis of Ethyl Levulinate from Furfuryl Alcohol

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
✓ 已验证 DOI 高影响因子
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CATALYSIS SURVEYS FROM ASIA · 2025 · IF 2.3

Spatial Configurational Construction of Pt-ZSM-5 Bifunctional Catalysts for Hydroisomerization of n-Heptane

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.

✓ 已验证 产品关联 DOI 高影响因子
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CRYSTENGCOMM · 2018 ·Vol. 20 ·期 40 ·6319-6327 · IF 3.304

Cooperative structure direction of organosilanes and tetrapropylammonium hydroxide to generate hierarchical ZSM-5 zeolite with controlled porous structure

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
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2023 · IF 4.2

Boosting the Production of Glycolic Acid from Formaldehyde Carbonylation via the Bifunctional PdO/ZSM-5 Catalyst

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
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ChemSusChem · 2022 ·Vol. 15 ·期 13 ·e202200233 · IF 9.14

Reductive Amination of 5-Hydroxymethylfurfural to 2,5-Bis(aminomethyl)furan over Alumina-Supported Ni-Based Catalytic Systems

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
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FOOD CHEMISTRY · 2018 · IF 4.946

Simultaneous quantification of free amino acids and 5′-nucleotides in shiitake mushrooms by stable isotope labeling-LC-MS/MS analysis

Meng Dong,Lei Qin,Jia Xue,Ming Du,Song-Yi Lin,Xian-Bing Xu,Bei-Wei Zhu

Evaluation of free amino acids (FAAs) and nucleotides in various food matrices has been a widely studied topic in recent years. Here, a fast and efficient strategy for the simultaneous analysis of 20 FAAs and six 5′-nucleotides, using stable isotope labeling-liquid chromatography coupled with tandem mass spectrometry (SIL-LC-MS/MS) is proposed. The method was validated with respect to selectivity, linearity, limits of detection (LOD) and quantification (LOQ), recovery, precision, and stability. LOQs of most FFAs were lower than 1 ng/mL, and 5′-nucleotides were in the range of 5–20 ng/mL. FAAs and 5′-nucleotides in ten shiitake mushrooms from different cultivate areas were further analyzed. Results showed that the contents of cytidine 5′-monophosphate, adenosine 5′-monophosphate, lysine, threonine, arginine were significantly different. Principal component analysis showed clear discrimination of origins, seasons and species. Thus, the proposed method is suitable for the fast discrimination of species and geographical origins of shiitake mushrooms.

研究领域: 食品科学 · 分析化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF CHEMICAL RESEARCH · 2016 · IF 0.661

Synthesis, Characterisation and Acetylcholinesterase-Inhibition Activities of 5-benzyl-1,3,4-thiadiazol-2-amine Derivatives

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
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2019 · IF 3.131

Preparation of degradable magnetic temperature- and redox-responsive polymeric/Fe3O4 nanocomposite nanogels in inverse miniemulsions for loading and release of 5-fluorouracil

Feng Gao,Xinlei Wu,Die Wu,Jianxing Yu,Jun Yao,Qi Qi,Zhihai Cao,Qinmin Cui,Yifang Mi

This work reports the synthesis of novel degradable magnetic temperature- and redox-responsive polymer/Fe 3 O 4 nanocomposite nanogels (NCGs) through inverse miniemulsion polymerization and their potential application as nanocarriers for controlled drug delivery. Surface of Fe 3 O 4 magnetic nanoparticles (MNPs) were vinyl-modified with 2-isocyanatoethyl methacrylate . Poly( N -vinylcaprolactam) (PNVCL)/Fe 3 O 4 NCGs were prepared via inverse miniemulsion polymerization by using a disulfide-containing cross-linker. The Fe 3 O 4 MNPs were chemically attached to the polymer matrix of NCGs, offering a good structural integrity of NCGs in aqueous systems. The PNVCL/Fe 3 O 4 NCGs not only inherited the good superparamagnetism of Fe 3 O 4 MNPs, but also displayed a reversible temperature-responsiveness as well as marked redox-responsiveness. The release behavior of a model anticancer drug 5-fluorouracil from the PNVCL/Fe 3 O 4 NCGs could be conveniently tuned by the external temperature, redox condition of media, or their combination. The prepared PNVCL/Fe 3 O 4 NCGs displayed a low cytotoxicity, holding a great potential in functioning as magnetic guiding nanocarriers for controlled drug delivery.

研究领域: 生物材料学 · 药物递送系统 · 高分子化学
✓ 已验证 DOI 高影响因子
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Journal of Environmental Chemical Engineering · 2021 · IF 5.909

Optimization of TiO2/ZSM-5 photocatalysts: Energy band engineering by solid state diffusion method with calcination

Xu Duan,Jian Yang,Guang Hu,Chen Yang,Yangfan Chen,Qingcai Liu,Shan Ren,Jiangling Li

In this work, based on a type of energy band engineering strategy as calcination , TiO 2 /ZSM-5 hybrids for photodegradation of methyl orange (MO) in water under UV light have been developed via a facile solid state diffusion method. Effects of varied calcination temperatures on TiO 2 /ZSM-5 hybrids have been systematically characterized including XRD , FT-IR, SEM, TEM , EDX mapping, BET, PL , EIS , UV–vis DRS, active species trapping experiments and Mott-Schottky curves. It was found that the calcination temperature influenced photocatalytic activity , typically on physicochemical properties of materials and adjustment for the energy gap and band position of TiO 2 . The XRD analysis revealed that hybridization of ZSM-5 kept the crystal phase of TiO 2 as anatase unchanged with the high-rising calcined temperature. The optimum sample calcined at 450 °C named as Z-T (450) presented nearly 99% degradation rate for MO, owing to optimal uniform distribution, highest specific surface area and best charge separation/transfer efficiency. The FT-IR comparison result that the functional groups and peak strength of the used catalyst were alike as before, showed the stability of photocatalyst . Adoption of calcination strategy does provide not only a clean, low-cost and highly efficient path to approach the complete degradation of azo dyes , but also a chance for photocatalytic technology to fulfill the implementation in industrial applications.

研究领域: 材料科学 · 环境化学 · 物理化学 · 催化化学 · 纳米材料 · 光催化技术
✓ 已验证 DOI 高影响因子
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CATALYSIS LETTERS · 2022 ·Vol. 153 ·期 6 ·1743-1755 · IF 2.936

Preparation of a Novel Composite Material Aluminum-Based MOF(DUT-5)/Bi2MoO6 for Degradation of Tetracycline

Zhou Yi,Yao Tiantian,Tan Yawen,Chen Yongbo,Chen Zhiyue,Zhang Jin

In this study, a novel composite DUT-5/Bi 2 MoO 6 (DUT-5/BMO) photocatalytic material was prepared by two-step hydrothermal method for the first time. The materials were characterized by SEM, XPS, etc. Studies have shown that material with a new n–n heterojunction structure can quickly degrade tetracycline. DUT-5 was embedded between the Bi 2 MoO 6 nanosheets, which promotes the photogenerated electrons from DUT-5 flows to Bi 2 MoO 6 , thereby reducing the recombination rate of photo-generated electron–hole pairs. The BET results show that the composite material has a larger specific surface area than the monomer Bi 2 MoO 6 . It can provide more active sites. After 60 min of visible light irradiation, the photocatalytic degradation efficiency of TC with 15% DUT-5/BMO reached 84.22%, which is 5.37 and 2.12 times higher than that of pure DUT-5 and Bi 2 MoO 6 , ·O 2 − and h + were the main active substances in the photocatalysis process. In addition, DUT-5/BMO composites show excellent stability and recyclability in 5 times cyclic experiments. In conclusion, DUT-5/BMO has good stability in the environment, and can be used for environmental remediation without pollution. Graphical

研究领域: 环境科学 · 材料科学 · 化学工程 · 纳米技术
✓ 已验证 DOI 高影响因子
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