Journal of Water Process Engineering
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2019
·
IF 3.173
Senlin Ma,Xingtao Zuo,Juan Xiong,Cong Ma,Zhongbing Chen
An ozonation process combined with hydrophobic adsorbent high silica ZSM-5 (HSZSM-5) was designed to enhance sulfamethoxazole (SMX) removal and reduce the ozone consumption. The promoted effect of HSZSM-5 on SMX removal was investigated in terms of SMX removal and TOC removal efficiency as well as the ozone consumption. The impacts of pH and CO 3 2− /HCO 3 - were also analyzed. The presence of HSZSM-5 helped to increase the SMX degradation and TOC removal efficiency and their kinetics rate constants. HSZSM-5 adsorption behaviors for SMX and its degradation intermediates were responsible for the findings. Direct ozone oxidation was the main mechanism of SMX removal as HZSM-5 could not contribute to producing H 2 O 2 and •OH. Much higher CO 3 2− /HCO 3 - concentration (≥10 mM) and pH value (>7) were in favor of SMX degradation. HSZSM-5 had a positive contribution to SMX removal. The mass ratio of ozone consumption to the removed SMX reduced to 0.63 g O 3 /g SMX. This system of introducing high silica zeolite in the ozonation/adsorption process is an environmentally and economically sound technology to removal micropollutants.
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JOURNAL OF CATALYSIS
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2019
·
IF 7.723
Rui Chen,Changjun Yang,Quanquan Zhang,Bingguang Zhang,Kejian Deng
A new iron tetra(2,3-bis(butylthio)maleonitrile)porphyrazine (FePz(SBu) 8 ) has been synthesized, then it was loaded on H-ZSM-5 zeolite to obtain a supported biomimetic photocatalyst H-ZSM-5/FePz(SBu) 8 . Using H 2 O 2 as oxidant, the photocatalytic selective oxidation of glucose in water under visible light (λ ≥ 420 nm) irradiation was carried out in presence of H-ZSM-5/FePz(SBu) 8 . Under such conditions, the glucose can be efficiently converted into value-added chemicals such as glucaric acid, gluconic acid, arabinose, glycerol and formic acid . More importantly, in comparison with pure FePz(SBu) 8 and pure H-ZSM-5 zeolite, the H-ZSM-5/FePz(SBu) 8 exhibited a higher photocatalytic activity for glucose oxidation and the formation of glucaric acid was observed only when H-ZSM-5/FePz(SBu) 8 was used, deriving from the synergistic effect between FePz(SBu) 8 and H-ZSM-5 zeolite. Some reaction parameters of glucose oxidation catalyzed by the H-ZSM-5/FePz(SBu) 8 were discussed, such as loading amount of FePz(SBu) 8 , H 2 O 2 :glucose ratio, glucose concentration, and so on. It was demonstrated that the Soret-band of FePz(SBu) 8 contributed more to the visible light photocatalytic activity than the Q-band during the photocatalytic process. The stability of H-ZSM-5/FePz(SBu) 8 during the photocatalytic process was further evaluated by the reusability test. In addition, the generation of reactive oxygen species was determined by electron spin resonance (ESR) technology and scavenger experiments. A possible reaction pathway of glucose oxidation was also discussed.
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ChemSusChem
·
2022
·Vol. 15
·期 13
·e202200233
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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.
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高影响因子
SOLID STATE SCIENCES
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2019
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IF 2.155
Yisong Wang,Tao Du,He Jia,Ziyang Qiu,Yanli Song
ZSM-5 zeolite with high aluminum content (Si/Al = 25) was synthesized and then cation-exchanged with alkali metal , alkaline earth metal , transition metal and rare earth metal cations (Li + , Mg 2+ , Ca 2+ , Cu 2+ , Zn 2+ , La 3+ and Ce 3+ ). Crystal structure and physicochemical properties were characterized by XRD , FTIR , TGA/DTG, XRF and nitrogen adsorption-desorption measurement. CO 2 adsorption isotherms of all samples were recorded approximately 0–120 kPa at 0 °C, 30 °C and 60 °C, and they were all successfully fitted by the Toth model. The N 2 adsorption isotherm presented an approximate straight rising line, and it was perfectly fitted by the Langmuir model. In addition, the CO 2 /N 2 adsorption selectivity, Henry's law constant and the working adsorption quantity were calculated by single component CO 2 and N 2 adsorption testing. Transition metal cations Cu 2+ and Zn 2+ type ZSM-5 had the maximum adsorption quantity of 0 °C (70.24 and 74.38 cm 3 /g), and they had the maximum adsorption selectivity under high pressure and adsorption saturation conditions. The adsorption heat of all ion-exchanged samples was lower than Na-ZSM-5, and it had the approximate value at high loadings (in the range of 15.46–17.65 kJ/mol).
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Catalysis Science & Technology
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2022
·Vol. 12
·期 21
·6437-6443
·
IF 6.177
Xingyu Lu,Ke Qi,Di Wang,Xueya Dai,Wei Qi
2,5-Furandicarboxylic acid (FDCA) is a high-value platform molecule that can replace the fossil derivative terephthalic acid in the synthesis of important chemicals. FDCA can be synthesized from the oxidation of the biomass derivative 5-hydroxymethylfurfural (HMF). In this study, we loaded Cu-based catalysts with different morphologies and chemical states on carbon paper, and it was found that the Cu nanocrystalline/carbon paper catalyst with a thin and scattered dendrite structure (Cu(NSD)/CP) exhibits the best performance for the electrooxidation of HMF (96% yield and 100% selectivity for FDCA), which is attributed to the fact that the Cu0 and Cu1+ species in the catalyst are easily oxidized in situ to Cu2+ species, showing high catalytic activity during the reaction process. This paper highlights the importance of the identification of active sites and the rational design of catalysts based on structure–function relations.
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Redox Biology
·
2025
·
IF 11.9
Xiaoyue Lai,Xiaoqin Wan,Xinyu Bao,Qingyuan Yang,Wei Zhang,Yan Tan,Xiaoshi Cai,Ziyang Wang,Yujie Li,Chun Liu,Zhongfang Deng,Pan Zheng,Dingyuan Tian,Ming Chen,Hongjun Yin,Gang Xu,Qi Huang,Zhihui Zhang,Hongmei Xia,Fang Deng
Hypoxia leads to decreased synthesis of 5-Methoxytryptophan (5-MTP) in pulmonary microvascular endothelial cells by downregulating Asmt level via Hif1α induced NF-κB p50 nuclear translocation. 5-MTP can reduce the localization of Prdx6 to lysosomes and increase its protein level by reducing its lysosomal degradation through interacting with Prdx6-S32, without affecting its function of clearing lipid peroxides (LPOs), thus improving the lipid peroxidation and rescuing VE-cadherin level and endothelial barrier function.
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ACS Synthetic Biology
·
2025
·
IF 3.9
Jing Wu,Ziqian Xiao,Yuhui Du,Minglan Luo,Jiacheng Zhang,Pei Guo,Zhipeng Chen,Binyuan Yang,Tingjian Chen
Aptamer-based sensors (aptasensors) have been extensively employed in biosensing and diagnostics. However, the broader application of aptasensors fabricated with DNA and RNA aptamers has been limited due to the intolerance of DNA and RNA to nucleases in biological fluids. A majority of sugar-modified nucleic acids, in particular 2’-F and 2’-OMe-modified nucleic acids, demonstrate a remarkable resistance to nuclease degradation and thus hold great potential in the development of more stable aptamers and aptasensors. In this work, employing enzymes including a laboratory-evolved polymerase for 2’-modified nucleic acids, we carried out systematic evolution of ligands by exponential enrichment (SELEX) experiments to obtain 2’-F/OMe-RNA aptamers for Bacillus cereus 5/B/6 metallo-β-lactamase (B. cereus 5/B/6 MBL), a crucial marker of many penicillin-resistant strains. Three aptamers composed of 2’-OMe-A, 2’-F-U, 2’-F-C, and 2’-OMe-G nucleotides (Apt-FUC1, Apt-FUC2, and Apt-FUC3) have been obtained and systematically characterized. All of them exhibited excellent target binding affinities, with equilibrium dissociation constant (Kd ) values of 95.9, 70.0, and 81.3 nM, and outstanding biological stability. Combining FAM-labeled Apt-FUC1, Apt-FUC2, and Apt-FUC3 with graphene oxide (GO), which could quench the fluorescence of FAM, we successfully constructed three sensitive and biologically stable 2’-F/OMe-RNA aptasensors for B. cereus 5/B/6 MBL, with the limit of detection (LOD) values of 0.38, 0.27, and 0.29 nM. Moreover, these three aptasensors all demonstrated good specificity for target detection in biological samples. This work has established a streamlined strategy for generating stable 2’-F/OMe-RNA aptamers and aptasensors, which should broaden the application of sugar-modified nucleic acids in biosensing and diagnostics.
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INORGANIC CHEMISTRY COMMUNICATIONS
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2025
·
IF 5.4
Tursunjan Aydan,Nuermaimaiti Yimamu,Ding Kaize,Yao Zhengzheng,Guan Qingqing
Metal-organic frameworks (MOFs), particularly UiO-66, offer advantages in biomass catalytic conversion due to their good thermal stability, tunable porosity and abundant active sites. However, agglomeration limits their catalytic efficiency. To address this, a series of acid-base bifunctional UiO-66-type catalysts supported on biochar (BC) was developed in green solution through a one-pot method. BC prepared by pyrolyzing cotton stalks (CS) under N 2 atmosphere at high temperature and activated before use. The physico-chemical properties of materials were studied by various characterization methods, and their catalytic performance for converting cellulose to 5-hydroxymethylfurfural (5-HMF) in [BMIM]Cl ionic liquid was evaluated. Reaction parameters such as catalyst type, catalyst loading, temperature and time were optimized. Under the optimized conditions, achieving a 5-HMF yield of 46.58 %. The BC-supported catalyst NH 2 -UiO-66-SO 3 H/BC exhibited significantly higher catalytic activity than its unsupported counterpart and increased the 5-HMF yield by 23.78 %. This performance improvement is attributed to the grafted sulfonic/amino groups, which enhance the catalytic performance by improving the dispersion of UiO-66 upon the introduction of BC. This work demonstrates biochar-supported UiO-66 as an effective strategy for enhancing catalytic efficiency in sustainable biomass valorization to platform chemicals.
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CANADIAN JOURNAL OF CHEMICAL ENGINEERING
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2025
·
IF 1.9
Xudong Wang,Yanyang Wu,Tianyou Wang,Bin Wu,Kui Chen,Lijun Ji
M-cresol and p-cresol, typically produced as mixtures in industrial processes, are crucial chemical intermediates. However, their separation is challenging due to their similar structures and properties. ZSM-5 zeolite has shown potential as an adsorbent for separation, while the performance is yet to be improved. In this study, ZSM-5-F(x) was synthesized via hydrothermal method, incorporating F − ions during the synthesis process. The adsorption behaviour of m-cresol and p-cresol on ZSM-5-F(x) was investigated through static experiments, with ZSM-5-F(8) demonstrating the highest selectivity (9.01). Both ZSM-5-F(0) and ZSM-5-F(8) were characterized using XRD, scanning electron microscopy (SEM), and Brunauer-Emmett-Teller (BET) techniques. In addition, the introduction of F − ions increased the material's electronegativity, as demonstrated by the change in zeta potential from 53.22 to −45.93 mV. Single-component adsorption of m-cresol or p-cresol on ZSM-5-F(0) and ZSM-5-F(8) respectively were investigated in detail. The adsorption of m-cresol on ZSM-5-F(8) showed a non-monotonic phenomenon with a significant decrease after 0.06 mol/L. The thermodynamic parameters including Δ G , Δ H , and Δ S were calculated accordingly. All the values |Δ G |, |Δ H |, and |Δ S | of both components on ZSM-5-F(8) were greater than those on ZSM-5-F(0), suggesting that the introduction of F − ions facilitated the adsorption. Competitive adsorption experiments on both ZSM-5-F(0) and ZSM-5-F(8) were conducted at 298.2 K. The results indicated that the selectivity α p/m on ZSM-5-F(8) increased with increasing initial concentration and laid between 13 and 14. After seven consecutive regeneration cycles, the selectivity (α p/m ) only decreased to 13. This study suggests that ZSM-5-F(8) could be a promising adsorbent for m-cresol and p-cresol in industrial applications.
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BIORESOURCE TECHNOLOGY
·
2025
·
IF 9
Fangyuan Zhou,Zhiyu Xiang,Hongke Zhang,Quan Bu,Wanbin Zhu,Wei Hu,Hongliang Wang
5-Hydroxymethylfurfural (HMF), regarded as a vital link between bio-refining and petrochemical refining, demonstrates significant potential to produce sustainable chemicals, fuels, and materials. However, its reliance on food-grade sugars as feedstock limits economic feasibility. This study demonstrates that sweet sorghum juice, rich in fructose, glucose, and sucrose, is an ideal, low-cost raw material for HMF production. Using HCl as catalyst, fructose in sweet sorghum juice was fully converted, yielding over 90% HMF in 80/20 (v/v) acetone/ water solvent system, with more than 85% of glucose retained for recycling. When AlCl 3 was used as catalyst, all sugars were efficiently converted, yielding over 70% HMF. Impurities in the pretreated juice did not impede sugar conversion but did partially neutralize the acidic catalyst. Techno-economic analysis revealed that utilizing sweet sorghum juice as feedstock produces HMF at a minimum selling price of $1909 per ton, a 39.6% reduction compared to fructose-based.
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Reaction Chemistry & Engineering
·
2025
·
IF 3.1
Wei Qi,Yuqi Chen,Liangzhi Li,Xin Ju,Hongwei Chen,Lishi Yan
The catalytic conversion of fructose to 5-hydroxymethylfurfural (5-HMF) in ternary deep eutectic solvent (DES)/methyl isobutyl ketone (MIBK) biphasic system at mild temperatures (50~70 ℃) was investigated in this work. The ternary DES consists of choline chloride (ChCl), benzene sulfonic acid (BSA) and ethylene glycol (EG) were physiochemical characterized by FT-IR and 1H NMR. The ternary DES(ChCl-BSA-EG)/MIBK biphasic system (ChCl/BSA/EG=2:1:1) resulted in 82.0% 5-HMF yield and 96.2% corresponding selectivity at 60 °C for 2 h. The kinetic analysis further revealed that the rate constant of fructose dehydration (k1) was much higher than the rate constant of 5-HMF conversion (k2). The calculated ratio of k1/k2 was 16.1. The proposed reaction mechanism suggested that the synergetic effect of the three components of ternary DES facilitates the elimination of water molecules from fructose and the formation of 5-HMF, while the MIBK extraction phase suppress the byproducts of 5-HMF as well. The present work provides a green and sustainable pathway for 5-HMF production with high yield and high selectivity at mild temperatures.
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INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
·
2025
·Vol. 26
·期 8
·3648
·
IF 4.9
Pize Xiao,Wei Mao,Zhiming Wu,Huimin Gao,Chutong Ling,Jinghong Zhou
A sustainable and efficient approach for converting carbohydrates into 5-hydroxymethylfurfural (HMF) via heterogeneous catalysis is crucial for effectively utilizing biomass. In this study, we synthesized a series of CrX-polyphenol-formaldehyde resin (PTF) catalysts, which are composites of Cr-doped phenolic-resin-based hydrothermal carbon, using a chelation-assisted multicomponent co-assembly strategy. The performance of the synthesized catalysts was assessed through various analytical techniques, including scanning electron microscopy, transmission electron microscopy, thermogravimetric analysis, X-ray photoelectron spectroscopy, pyrolysis–Fourier transform infrared spectroscopy, and Brunauer–Emmett–Teller analysis. Cr incorporation into the catalysts enhanced the total and Lewis acidities. Notably, the optimized catalyst, designated as Cr0.6-PTF, achieved an effective glucose conversion into HMF, yielding a maximum of 69.5% at 180 °C for 180 min in a saturated NaCl solution (NaClaq)/dimethyl sulfoxide (2: 18) solvent system. Furthermore, Cr0.6-PTF maintained excellent catalytic activity and a stable chemical structure after nine cyclic reactions, resulting in a 63.8% HMF yield from glucose. This study revealed an innovative approach for utilizing metal-doped phenolic resin hydrothermal carbon to transform glucose into platform chemicals.
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危险品化学品经营许可证（带存储）