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MOLECULES · 2024 ·Vol. 29 ·期 16 ·3779 · IF 4.2

Zirconium Phosphate-Pillared Zeolite MCM-36 for Green Production of γ-Valerolactone from Levulinic Acid via Catalytic Transfer Hydrogenation

Pan Hou,Haopeng Su,Keyan Jin,Qiang Li,Wenfu Yan

γ-valerolactone (GVL), derived from biomass, is a crucial platform compound for biofuel synthesis and various industrial applications. Current methods for synthesizing GVL involve expensive catalysts and high-pressure hydrogen, prompting the search for greener alternatives. This study focuses on a novel zirconium phosphate (ZrP)-pillared zeolite MCM-36 derivative catalyst for converting levulinic acid (LA) to GVL using alcohol as a hydrogen source. The incorporation of ZrP significantly contributes to mesoporosity and greatly enhances the acidity of the catalysts. Additionally, we employed31P MAS NMR to comprehensively investigate the influence of phosphorus species on both the acidity and the catalytic conversion of LA to GVL. By adjusting the Zr-to-P ratios, we synthesized catalysts with enhanced acidity, achieving high conversion of LA and selectivity for GVL. The catalyst exhibited high recyclability, showing only minor deactivation over the course of five cycles. Furthermore, the catalyst was successfully applied to the one-pot conversion of furfural to GVL, showcasing its versatility in biomass conversion. This study highlights the potential of the MCM-ZrP1 catalyst for sustainable biomass conversion and offers insights for future research in renewable energy technologies.

CAS / MDL: 111-49-9 13520-92-8
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NEW JOURNAL OF CHEMISTRY · 2025 · IF 2.5

γ-Cyclodextrin metal-organic framework enhanced the bioavailability of vitexin in rats by increasing solubility and inhibiting re-crystallization

Qinghua Ni,Qiao Chen,Haixia Xu,Wenjun Wang,Zhongping Yin,Qing-Feng Zhang

γ-Cyclodextrin metal-organic frameworks (γ-CD-MOFs) were prepared by using γ-CD and KOH as the raw materials. The γ-CD-MOFs showed a cubic shape with particle size in the range of 400~700 nm and Langmuir surface area of 406.88 m2/g. The γ-CD-MOFs were used as the carrier of vitexin through adsorption in methanol, and the loading capacity was 34.9 mg/g. XRD showed that vitexin lost its crystal structure and FTIR showed vitexin had secondary interaction with the carrier. The structure of γ-CD-MOFs collapsed quickly in water, thereby rapidly releasing the loaded vitexin. Through the carrier, the water solubility of vitexin was increased from 31.79 μg/mL to 581.78 μg/mL in simulated gastric fluid at 37 oC, which was increased by about 18.3 times. Meanwhile, the presence of γ-CD inhibited the re-crystallization of vitexin and maintained its supersaturated status through formation of complexes. A pharmacokinetic study showed that the oral bioavailability of vitexin was enhanced by 1.99 times in rats through γ-CD-MOFs carrier.

CAS / MDL: 3681-93-4
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Foods · 2025 ·Vol. 14 ·期 15 ·2733 · IF 5.1

Dual Bioconversion Strategy: Synergistic Germination and Lactobacillus Fermentation Engineering for a γ-Aminobutyric Acid-Enriched Beverage from Brown Rice

Di Yuan,Shan Zhang,Bin Hong,Shan Shan,Jingyi Zhang,Dixin Sha,Shiwei Gao,Qing Liu,Shuwen Lu,Chuanying Ren

Growing demand for plant-based nutraceuticals drives the need for innovative bioprocessing strategies. This study developed an integrated approach combining germination and Lactobacillus-mediated fermentation to produce a γ-aminobutyric acid (GABA)-enriched functional beverage from brown rice. Systematic screening identified an optimal rice cultivar for germination. Sequential enzymatic liquefaction and saccharification were optimized to generate a suitable hydrolysate. Screening of 13 probiotic strains revealed that a 10-strainLactobacillus–Bifidobacteriumconsortium maximized GABA synthesis (12.2 mg/100 g). Fermentation parameters were optimized to 0.25% monosodium glutamate, 4% inoculum, 10 μmol/L pyridoxine hydrochloride, 37 °C, and 24 h. The resulting beverage achieved significantly elevated GABA concentrations while exhibiting low fat (0.2 g/100 g), reduced caloric content (233.6 kJ/100 g), and high viable probiotic counts (2 × 108CFU/g). This strategy demonstrates significant potential for the scalable production of multifunctional, plant-based nutraceuticals with targeted bioactive components.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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INDUSTRIAL CROPS AND PRODUCTS · 2024 · IF 5.6

One-pot cascade process for efficient upgrading of furfural to γ-valerolactone over adjustable Lewis-Brønsted bi-acidic catalyst

Jiarong Qiu,Yi Liu,Jingwen Zhang,Ben Zhou,Qiyue Yang,Liangqing Zhang,Jianfeng Chen,Bingshu Wang,Lu Lin,Xianhai Zeng

A series of zirconium phosphate (ZrP) loaded H-beta-25 zeolite (i.e., ZrP@HB) multifunctional composite catalysts were synthesized by a simple co-precipitation method, and the one-pot upgrading for the transfer hydrogenation of furfural to γ-valerolactone (GVL) was systematically investigated through various characterizations and catalytic evaluation experiments. Comparative characterization analysis of the ZrP@HB-X(Y) catalysts showed that the ZrP@HB-4(4) catalyst has uniform distribution of elements, exhibiting a large specific surface area and hierarchical mesoporous/microporous structure. Fourier transform infrared spectroscopy of pyridine (Py-FTIR) and NH 3 temperature-programmed desorption characterizations indicated the presence of Lewis and Brønsted acid sites, as well as weak, moderate, and strong acid sites in the ZrP@HB-4(4) catalyst. It was confirmed by X-ray photoelectron spectroscopy and FTIR that the main reason for Lewis and Brønsted acid sites formation is the presence of P-O-Zr, P-O-H, and HB zeolite on the ZrP@HB-4(4) catalyst. The HB zeolite as well as Zr and P ratio, can be easily adjusted to efficiently regulate the acidity strength and Lewis and Brønsted acid sites of the ZrP@HB-X(Y) catalysts. The catalytic experiments demonstrated that the physicochemical properties of the ZrP@HB-4(4) catalyst mentioned above significantly enhance the GVL production. Notably, Lewis and Brønsted acid sites as well as transition metal sites of Zr in the ZrP@HB-4(4) catalyst were identified as the main factors that enhance the yield of the target product. By optimizing the reaction conditions, the yield of GVL could be as high as 88.16%. Reusability experiments demonstrate that the ZrP@HB-4(4) catalyst possesses excellent stability. Using levulinic acid as the substrate, the yield of GVL reached 93.92%, suggesting its potential versatility.

CAS / MDL: 7722-76-1 108-29-2
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BIOCONJUGATE CHEMISTRY · 2020 · IF 4.031

A New γ-Glutamyltranspeptidase-Based Intracellular Self-Assembly of Fluorine-18 Labeled Probe for Enhancing PET Imaging in Tumors

Siqin Ye,Shijie Wang,Dingyao Gao,Ke Li,Qingzhu Liu,Bainian Feng,Ling Qiu,Jianguo Lin

γ-Glutamyltranspeptidase (GGT) is a cell -membrane-associated enzyme which has been recognized as a promising biomarker for the diagnosis of many malignant tumors. Herein, we rationally designed a fluorine-18 labeled small-molecule probe, [18F]γ-Glu-Cys(StBu)-PPG(CBT)-AmBF3 (18F-1G), by applying a biocompatible CBT-Cys condensation reaction and ingeniously decorating it with a GGT-recognizable substrate, γ-glutamate (γ-Glu), for enhancing PET imaging to detect GGT level of tumors in living nude mice. The probe had exceptional stability at physiological conditions, but could be efficiently cleaved by GGT, followed by a reduction-triggered self-assembly and formation of nanoparticles (NPs) progressively that could be directly observed by transmission electron microscopy (TEM). In in vitro cell experiments, 18F-1G showed GGT-targeted uptake contrast of 2.7-fold to that of 18F-1 for the detection of intracellular GGT level. Moreover, the higher uptake in GGT overexpressed HCT116 tumor cells (∼4-fold) compared to GGT-deficient L929 normal cells demonstrated that 18F-1G was also capable of distinguishing some tumor cells from normal cells. In vivo PET imaging revealed enhanced and durable radioactive signal in tumor regions after 18F-1G coinjecting with 1G, thus allowing real-time detection of endogenous GGT level with high sensitivity and noninvasive effect. We anticipated that our probe could serve as a new tool to investigate GGT-related diseases in the near future.

✓ 已验证 DOI PubMed 高影响因子
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ACS ES&T Water · 2021 · IF 0

Continuous Catalytic Ozonation of Antibiotics Using Mn and Cu Oxides on γ-Al2O3 Pellets in a Micropacked Bed Reactor

Qiang Cao,Fengyan Lou,Na Liu,Jisong Zhang,Lidong Wu

Today, the Al2O3-supported catalyst in the heterogeneous catalytic ozonation system attracts attention due to its stable structure and relatively high surface activity. Herein, Mn and Cu oxides loaded on γ-Al2O3 pellets were prepared using an impregnation method to improve the removal efficiency in a micropacked bed reactor (μPBR). The effects of the initial pH, the ratio of O3 to chemical oxygen demand (COD), and HO• scavenger on the catalytic performance were investigated. Experimental results showed that the MnO2/γ-Al2O3 and CuO/γ-Al2O3 catalysts exhibited excellent catalytic performance. The COD removal efficiencies were 86.3% for CuO/Al2O3, 76.9% for MnO2/Al2O3, 71.6% for Al2O3, and 35.8% for ozone alone within 71 s. Compared with those of batch reactors, the apparent degradation rate constant of COD with prepared catalysts in a μPBR increased by 2–3 orders of magnitude. In addition, the CuO/γ-Al2O3 catalyst maintained a relatively stable activity in the continuous flow test for a long time (100 h). Finally, some typical antibiotics were treated by catalytic ozonation in a μPBR. The removal efficiencies of these antibiotics and COD reached approximately 100.0% and 62.9–87.8% within 71 s, respectively. Thus, the continuous catalytic ozonation system with the CuO/γ-Al2O3 catalyst based on μPBRs could be a promising pathway for the treatment of industrial wastewater with antibiotics.

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RSC Advances · 2020 ·Vol. 10 ·期 29 ·17154-17162 · IF 3.119

MOF-derived (MoS2, γ-Fe2O3)/graphene Z-scheme photocatalysts with excellent activity for oxygen evolution under visible light irradiation

Ang Li,Yuxiang Liu,Xuejun Xu,Yuanyuan Zhang,Zhichun Si,Xiaodong Wu,Rui Ran,Duan Weng

Constructing Z-scheme heterojunctions is considered as an effective strategy to obtain catalysts of high efficiency in electron–hole separation in photocatalysis. Unfortunately, suitable heterojunctions are difficult to fabricate because the direct interaction between two semiconductors may lead to unpredictable negative effects such as electron scattering or electron trapping due to the existence of defects which causes the formation of new substances. Furthermore, the van der Waals contact between two semiconductors also results in bad electron diffusion. In this work, a MOF-derived carbon material as a Z-scheme photocatalyst was synthesized via one-step thermal treatment of MoS2 dots @Fe-MOF (MIL-101). Under visible light irradiation, the well-constructed Z-scheme (MoS2, γ-Fe2O3)/graphene photocatalyst shows 2-fold photocatalytic oxygen evolution activity (4400 μmol g−1 h−1) compared to that of γ-Fe2O3/graphene (2053 μmol g−1 h−1). Based on ultraviolet photoelectron spectrometry (UPS), Mott–Schottky plot, photocurrent and photoluminescence spectroscopy (PL) results, the photo-induced electrons from the conduction band of γ-Fe2O3 could transport quickly to the valence band of MoS2 via highly conductive graphene as an electron transport channel, which could significantly enhance the electron–hole separation efficiency as well as photocatalytic performance.

✓ 已验证 DOI PubMed 高影响因子
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SCIENCE OF THE TOTAL ENVIRONMENT · 2020 · IF 6.551

γ-ray induced formation of oxygen vacancies and Ti3+ defects in anatase TiO2 for efficient photocatalytic organic pollutant degradation

Caifeng Zhao,Yahui Yang,Lin Luo,Sai Shao,Yiji Zhou,Ying Shao,Faqi Zhan,Jian Yang,Yaoyu Zhou

Oxygen vacancies and Ti 3+ defects in anatase TiO 2 have attracted great attention to address the insufficient optical absorption and photoinduced charge-carrier separation in photocatalysis . In this study, we demonstrate a superficial and innovative approach for synthesizing anatase TiO 2 nanoparticles with abundant oxygen vacancies via γ-ray irradiation reduction at room temperature. X-ray photoelectron spectroscopy (XPS) and electron paramagnetic resonance (EPR) confirm that oxygen vacancies and Ti 3+ defects can be quantitatively and extensively obtained by merely regulating the irradiation dosage. Photoelectrochemical measurements suggest that oxygen vacancies and Ti 3+ defects promoted the separation of electron-hole pairs and then enhanced the photocatalytic degradation performance for organic pollutant. In comparison with TiO 2 (no irradiation), the sample (49.5 kGy irradiation) exhibited a 20.0-fold enhancement in visible-light decomposition of phenol. In addition, the results of scavenge experiments and mechanism analysis revealed that O 2 − are the dominant active species. The excited electrons generated at the conduction band and oxygen vacancy level of TiO 2−x -49.5 conspicuously contributes to generate much more ·O 2 − species. This novel study shows at room temperature, the γ-ray approach of irradiation leads to faster formation and quantification of oxygen vacancies in the semiconductor materials .

✓ 已验证 DOI PubMed 高影响因子
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PARTICLE & PARTICLE SYSTEMS CHARACTERIZATION · 2017 ·Vol. 34 ·期 3 ·1600430 · IF 4.474

Monodisperse Polypyrrole Nanoparticles Prepared via γ-Ray Radiolysis of Water: An Efficient Near-Infrared Photothermal Agent for Cancer Therapy

Jie Wang,Jielin Rong,Zhong Fang,Mozhen Wang,Anila Asif,Qichao Wu,Xiao Zhou,Xuewu Ge

Biosafe nanoparticles with strong near-infrared (NIR) light photothermal conversion effect can bring effective hyperthermia as one of the promising approaches in cancer therapy. In this work, a new facile and green preparation method of polypyrrole (PPy) nanoparticles based on 60 Co γ-ray radiation on a simple air-saturated strong acidic aqueous solution of pyrrole (pH ≤ 1) is studied. According to the MCAP-FACSIMILE simulation on the concentrations of the radiolysis products of water at the presence of H + and O 2 , the main strong oxidative radiolysis products · OH and H 2 O 2 rapidly induce the polymerization of pyrrole. The size of the prepared PPy nanoparticles is about several tens of nanometers and can be controlled by the pH, the concentration of the stabilizer poly(vinyl alcohol), and the absorbed dose rate (the amount of energy absorbed per unit mass of the irradiated material within per unit of time). The PPy nanoparticles show rapid and remarkable NIR (808 nm) photothermal conversion efficiency up to 40.1% in water. Furthermore, the in vitro and in vivo experiments confirm that the prepared PPy nanoparticles exhibit enough strong NIR photothermal effect in tumor cells (4T1 and HeLa) and show a promising prospect as the NIR photothermal agent for the future cancer therapy.

✓ 已验证 DOI 高影响因子
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FUEL · 2023 · IF 7.4

Effect of carbon modifier on characteristics and catalytic properties of zeolite–carbon hybrid supported Zr towards γ-valerolactone production

Zhongdi Liu,Rui Zhang,Huai Liu,Junhua Zhang,Yong Sun,Naya Li,Lincai Peng

Developing efficient and stable solid functional materials for the catalytic upgrading of biomass-based platform furanic molecules is of great significance to produce value-added chemicals and biofuels. We herein report β-zeolite (β)/biobased carbon hybrids supported Zr species towards the cascade conversion of furfural into γ-valerolactone (GVL) with high activity and favorable stability. The role and importance of carbon modifier were highlighted. The cellulose (CEL) modified Zr/β-CEL catalyst was found to be uniquely effective, leading to an increase of GVL yield from 49.3% to 81.1%. Catalyst characterizations revealed that the structural integrity of β was largely preserved using CEL as the carbon modifier, accompanied by the increased mesopore volume and pore size for better accessibility of active sites and diffusion of reactants. Simultaneously, the presence of CEL offered an appropriate ratio of Lewis and Brønsted acid sites due to the well incorporation and dispersion of Zr species, which ensured the successive transfer hydrogenation and ring-opening reactions. Kinetic studies demonstrated the positive effect of CEL modification on reducing the apparent activation energy and thereby facilitating the GVL formation. More importantly, Zr/β-CEL with enhanced structural stability also exhibited markedly higher recyclability compared with the pristine Zr/β. The understanding on the roles of carbon modifier can be employed to optimize the physicochemical properties of zeolite-based catalysts for roundly improving the catalytic reactivity of biomass-related compounds.

✓ 已验证 DOI 高影响因子
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RSC Advances · 2013 ·Vol. 3 ·期 26 ·10277-10284 · IF 2.562

Conversion of biomass-derived ethyl levulinate into γ-valerolactone via hydrogen transfer from supercritical ethanol over a ZrO2 catalyst

Xing Tang,Lei Hu,Yong Sun,Geng Zhao,Weiwei Hao,Lu Lin

A green and efficient process was developed for the conversion of biomass-derived ethyl levulinate (EL) into γ-valerolactone (GVL) using supercritical ethanol as the hydrogen donor and the reaction medium over low-cost and eco-friendly ZrO2 catalysts, which were prepared by the precipitation method and characterized by BET, SEM, XRD, FT-IR, TGA-DTA, TPD-NH3 and TPD-CO2. The results indicated that amorphous ZrO2 with a high specific surface area and a large number of acid–base sites exhibited the highest catalytic activity, an excellent GVL yield of 81.5% with 95.5% EL conversion was achieved at 523 K over 3 h. In addition, combined with the results of poisoning experiments, a plausible mechanism of catalytic transfer hydrogenation (CTH) via a six-membered ring transition state was also presented.

✓ 已验证 DOI 高影响因子
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RSC Advances · 2018 ·Vol. 8 ·期 2 ·724-731 · IF 2.936

Mechanism and effect of γ-butyrolactone solvent vapor post-annealing on the performance of a mesoporous perovskite solar cell

Jun Luo,Ren Zheng Qiu,Zhi Sheng Yang,Yan Xiang Wang,Qi Feng Zhang

In this paper, γ-butyrolactone (GBL) solvent vapor post-annealing (SVPA) on CH3NH3PbI3 thin films is reported, aiming to improve the complete transformation of PbI2 and increase the grain size of the CH3NH3PbI3 crystal, thus boosting the performance of mesoporous CH3NH3PbI3 perovskite solar cells (PSCs). The influence of GBL SVPA on the microstructure of perovskite layers and performance of PSCs was studied. The short circuit current density (Jsc) of the devices significantly increased, yielding a high efficiency of 16.58%, which was 27.05% higher than that of thermally annealed films. A model was derived to explain the effect of GBL SVPA on PSCs. The perovskite films prepared by this method present several advantages such as complete transformation of PbI2 to CH3NH3PbI3, high crystallinity, large grain size, and fewer grain boundaries than those prepared without GBL SVPA. This improvement is beneficial for charge dissociation and transport in hybrid photovoltaic devices.

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