JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2025
·
IF 9.7
Yu Wang,Qilin Zhao,Qi Fang,Jian Sun,Yan Du,Haji Akber Aisa
Enzyme cascades have attracted widespread attention owing to the exceptional specificity and efficient signals transduction, however, constrained by the high cost and limited stability of bio-enzymes. In this study, a novel mimic multienzyme nanoreactor (GOx@MAF-7(Fe), i.e. GMF) was developed through a one-step encapsulation of glucose oxidase (GOx) into a metal azolate framework, MAF-7(Fe). Benefiting from the synergistic effect of GOx and the exceptional peroxidase-like (POD) activity of MAF-7(Fe), GMF enabled a robust cascade catalytic reaction for colorimetric sensing. The unique structural and functional properties of MAF-7(Fe) not only facilitated efficient enzyme immobilization but also enhanced the stability of GOx, outperforming free enzymes in terms of storage and thermal tolerance. The GMF-based platform demonstrated high sensitivity and selectivity in glucose response. More importantly, by integrating α-glucosidase (α-Glu) into a three-enzyme cascade system, a colorimetric assay was successfully developed for α-Glu activity with a detection limit of 0.25 mU/mL, surpassing most existing methods. This platform was further applied for α-Glu inhibitor screening, with acarbose as a model inhibitor, and achieved precise quantification of inhibition efficiency (IC 50 = 60.06 nM). This work not only establishes a versatile and efficient sensing platform for diabetes-related biomolecule detection but also pioneers a novel strategy for enzyme immobilization and multienzyme cascade construction, opening new avenues for multifunctional material design in biomedical research.
研究领域:
生物化学
·
材料科学
·
医学检测
✓ 已验证
产品关联
DOI
PubMed
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2020
·
IF 16.683
Yingguang Zhang,Muyan Wu,Yifei Wang,Yu Ho Kwok,Wending Pan,Wai Szeto,Haibao Huang,Dennis Y.C. Leung
The particular role of fluorine (F) doping in the photocatalytic activity of nanocrystalline titanium dioxide (TiO 2 ) towards toluene degradation was systematically studied. TiO 2 nanosheet catalysts doped with different amounts of F − (denoted by F-TiO 2 ) were synthesized by hydrothermal method. For comparison, calcination was performed on the catalyst to remove F - . The photocatalytic oxidation (PCO) of toluene over F-TiO 2 was found to be much higher than those of TiO 2 and commercial P25 under the irradiation of vacuum ultraviolet (VUV) light, with a high toluene degradation efficiency of about 90 %. Moreover, the toluene degradation efficiency increased to 96 % with the addition of only 1 wt.% α-MnO 2 nanowires, and the residual ozone (O 3 ) in the system can be completely eliminated. In addition, four different substrates were explored for catalyst coating to facilitate the operation and minimize catalyst loading, which can provide a promising strategy for practical volatile organic compounds (VOCs) abatement in industrial applications.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
高影响因子
Journal of Environmental Sciences
·
2019
·
IF 3.556
Shanshan Su,Yuyang Liu,Wei He,Xianchun Tang,Wei Jin,Yaping Zhao
Persulfate activation has been applied as one of the efficient advanced oxidation processes (AOPs) to remediate polluted environments. In this study, a novel α-FeOOH anchored by graphene oxide (GO)-carbon nanotubes (CNTs) aerogel (α-FeOOH@GCA) nanocomposite activated persulfate system (α-FeOOH@GCA + K 2 S 2 O 8 ) was applied for decolorization of Orange II (OII). The decolorization of OII was remarkably enhanced to a level of ~ 99% in this system compared with that of pristine α-FeOOH (~ 44%) or GO-CNTs (~ 18%). The enhanced catalytic activity of α-FeOOH@GCA was due to the formation of a heterojunction by α-FeOOH and GO-CNTs as confirmed by the presence of Fe–O–C chemical bonds. The degradation intermediates of OII were comprehensively identified. The proposed degradation pathway of OII begins with the destruction of the conjugated structures of OII by the dominant reactive oxygen species , surface-bound SO 4 •− . The decolorization efficiency of OII by the α-FeOOH@GCA activated persulfate system decreased from the first to third cycle of recycling. Ultraviolet (UV) irradiation or introduction of a small amount of Fe 2+ could restore the activation of this system. The results show that the α-FeOOH@GCA persulfate activation system promises to be a highly efficient environmental remediation method for organic pollutants .
研究领域:
环境科学
·
化学工程
✓ 已验证
DOI
高影响因子
GREEN CHEMISTRY
·
2017
·Vol. 19
·期 20
·4838-4848
·
IF 9.125
Gang Wang,Yiming Xu,Suojiang Zhang,Zengxi Li,Chunshan Li
A one-pot synthesis of α,β-unsaturated esters from unactivated esters and aldehydes using strong bases, such as sodium alkoxide and potassium tert-butoxide, was reported. However, the ionic liquid (IL) catalyzed probase method for producing α,β-unsaturated esters was not reported until now. In this work, a series of ILs with fluoride anions were firstly prepared and used as catalysts in combination with the probase N,O-bis(trimethylsilyl) acetamide (BSA) for the α,β-unsaturated esters synthesis. This process could also be promoted through the introduction of another IL with Lewis acid sites. The yield and selectivity of the product could reach up to 84.2% and 95.0%, respectively, when [Bmim]F was used in combination with [Bmim]Cl/AlCl3 (the molar fraction of AlCl3 is 0.67). The mechanism investigation through GC-MS indicates that BSA would convert into onium amide, which acted as a strong base for α-H abstraction, with the catalysis of [Bmim]F. Meanwhile, [Bmim]Cl/AlCl3 played an important role in the condensation step between enolates and aldehydes. On the basis of mechanism insights, kinetic and thermodynamic studies were also carried out for a better understanding of this new route.
研究领域:
有机化学
·
催化化学
✓ 已验证
DOI
高影响因子
Catalysis Science & Technology
·
2015
·Vol. 6
·期 6
·1693-1700
·
IF 5.426
Zhixin Zhang,Yehong Wang,Min Wang,Jianmin Lu,Chaofeng Zhang,Lihua Li,Jingyang Jiang,Feng Wang
We herein report the oxidative C–C coupling of ketones and primary alcohols to produce α,β-unsaturated ketones in the absence of base additives. This cascade synthetic reaction was conducted at 150 °C in 12 h using a heterogeneous CeO2 catalyst. The conversion of acetophenone reached 74% with 89% selectivity to chalcone. A correlation between the CeO2 crystal plane and catalytic performance is established as the catalytic activities decrease in the sequence of (110) > (111) > (100). Characterization using Raman spectroscopy, CO2 temperature-programmed desorption (CO2-TPD), and in situ active site-capping tests has shown that the unusual catalysis of the CeO2 catalyst is attributed to the coexistence of basic and redox active sites. These sites synergistically catalyze the oxidation of alcohols to aldehydes and the aldol condensation to ketones. Moreover, the CeO2 catalyst can be reused several times after calcination to remove the surface-adsorbed substances.
研究领域:
化学
·
催化科学
✓ 已验证
DOI
高影响因子
ACS Applied Materials & Interfaces
·
2025
·
IF 8.2
Haozhang Xu,Guoan Xi,Wei Chen,Yin Hu,Jun Xia,Weiguo Song,Changyan Cao,Yanhong Zeng,Dan Zhou
The development of hydrogenation catalysts with high performance and stability could decrease the byproducts and simplify the follow-up process in the industrial process. Optimizing supported catalysts through support improvement is a feasible approach to balance effectiveness and cost. In view of this, cubic perovskite NaNbO3 was modified with organosiloxane to form a heterophase junction support consisting of amorphous silica and NaNbO3 crystal. On the basis of this, the supported Ru catalyst displayed superior performance for α-pinene hydrogenation with almost complete conversion, cis-pinane selectivity, and good stability. The relationship between the structure and performance of the catalyst was systematically investigated by comprehensive experiments and multiple characterization technologies. Due to the formation of the heterophase junction, the surface hydrophobicity, specific surface area, and electron properties of the catalyst were optimized, leading to the good dispersity of the catalyst in the hydrogenation mixture and excellent adsorption and charge transfer ability, which should account for the unique performance of the catalyst, as confirmed by a series of experiments, characterizations, and DFT calculations. This work proposes an effective approach to optimize the surface structure and electronic properties of the catalysts through constructing crystallized and amorphous heterophase junction support, which is theoretically significant for the design and development of cost-effective heterogeneous hydrogenation catalysts.
研究领域:
催化化学
·
材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
MICROCHIMICA ACTA
·
2025
·Vol. 192
·期 6
·1-11
·
IF 5.3
Chen Yun-Ting,Han Jing-Wen,Yu Zi-Wei,Yang Ruo-Yu,Wu Mei-Juan,Huang Pin-Fang,Liu Meng-Meng
A decentralized electrochemical immunosensor was developed using a smartphone and a portable electrochemical workstation. The system employs a gold nanoflower-modified screen-printed carbon electrode (AuNFs/SPCE) for the sensitive measurement of adalimumab (ADL) in human serum via antigen‒antibody recognition. Scanning electron microscopy, X-ray photoelectron spectroscopy, and atomic force microscopy were used to investigate the AuNFs/SPCE. Compared with the bare SPCE, the AuNFs/SPCE has a 1.47-fold larger specific surface area, which enhances the capture efficiency of ADL for signal amplification. Electrode modification and antigen‒antibody assembly processes are characterized by cyclic voltammetry and electrochemical impedance spectroscopy. The immunosensor achieves excellent electrochemical properties by optimizing experimental conditions, which improves the signal-to-noise ratio and thus the analytical performance. Under the best experimental conditions, the immunosensor has a quantitative range of 0.05‒4 μg/mL in diluted human serum with a detection limit of 9.1 ng/mL, which is consistent with the effective therapeutic window of ADL in clinical settings. The prepared electrodes maintain 10-day stability, while with high reproducibility at different ADL concentrations. High recoveries in the range 94.08‒108.6% are obtained in human serum samples. Furthermore, ADL in the serum samples was measured by both ELISA and the developed sensor. Pearson and Bland‒Altman analyses revealed a consistent trend between the two methods. Therefore, this immunosensor is a promising tool for the point-of-care (POC) measurement of ADL in clinical samples, providing valuable insights for personalizing ADL dosing regimens in clinical practice. Graphical
研究领域:
生物医学工程
·
临床检验
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2024
·Vol. 31
·期 13
·20621-20636
·
IF 0
Yin Bingjie,Li Jingying,Guo Wei,Dong Haoqing,Zhang Guangshan,Xin Yanjun,Zhang Guodong,Chen Qinghua
Polycyclic aromatic hydrocarbons (PAHs) in soil are potentially harmful to human health. However, the use of photocatalysis technology to treat soil contaminated with PAHs remains challenging. Therefore, TiO 2 /α-FeOOH composite photocatalyst has been synthesized by hydrothermal method and sol–gel method and applied to photocatalytic degradation of fluoranthene in soil. The morphology, elements, crystal structure, optical properties, electrochemical characteristics, and photocatalytic activity of TiO 2 /α-FeOOH have been characterized. Results showed that TiO 2 is tightly fixed on the surface of α-FeOOH, and TiO 2 /α-FeOOH had higher photocatalytic activity on photocatalytic degradation of fluoranthene in soil under simulated sunlight. The degradation efficiency of TiO 2 /α-FeOOH is 3.0 and 4.8 times higher than that of TiO 2 and α-FeOOH, respectively. This is attributed to enhanced photocatalytic ability by enhancing the transfer capacity of electrons and holes and broadening the spectrum absorption range. The highest degradation efficiency was achieved when the pH of the soil is neutral, the ratio of water/soil is 10:1, and the dosage of catalyst is 50 mg/g. In addition, it was proved that •O 2 − , h + , and 1 O 2 are the main active substances in the photocatalysis of TiO 2 /α-FeOOH. The possible mechanism of a Z-type electron transfer structure was also proposed. The degradation products of fluoranthene were detected, and the degradation pathway was deduced.
研究领域:
环境科学
·
材料科学
·
催化
·
土壤修复
·
纳米技术
✓ 已验证
DOI
ACS Applied Materials & Interfaces
·
2020
·
IF 8.758
Yingying Yin,Lei Zhu,Xiao Chang,Jinwei Xue,Shifan Yu,Xiaofang Li,Qingzhong Xue
Designing and constructing a stable water-retention layer acting as the isolation between the oil and membrane surface holds great significance for solving the membrane fouling problems in oil/water separation, including common layered oil/water mixtures, immiscible oil-in-water emulsions, and even high-viscosity crude oil-in-water emulsions. Inspired by the self-cleaning property of sea urchin thorns, a bioinspired anti-oil-fouling hierarchically structured membranes decorated with urchin-like α-FeOOH particles was successfully prepared via the layer-by-layer (LBL) self-assembly method, maintaining numerous effective micro-nanopores. The hierarchical structured membrane exhibited superior superhydrophilicity/underwater superoleophobicity, high water-retention ability, and preferable anti-oil-fouling properties. Furthermore, the biomimetic membrane with controllable pore sizes could not only separate common layered oil/water mixtures but also effectively separate immiscible surfactant-stabilized oil-in-water emulsions of both low-viscosity crude oil and high-viscosity crude oil with an ultrahigh water flux up to 2598.4 L m–2 h–1 and an outstanding separation efficiency of 98.5%, revealing its promising prospect in oily wastewater treatment.
研究领域:
材料科学
·
环境工程
·
生物仿生学
✓ 已验证
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2023
·Vol. 35
·期 1
·1-13
·
IF 2.8
Sun Qin,Yang Wanchun,Hu Zhongyu,Jia Gaozhi,Wang Yangyang
Copper pastes are widely used in metallization of ceramic surfaces but are limited by poor oxidation resistance, high resistivity, and low bonding strength. In this work, the 30Bi 2 O 3 –55B 2 O 3 –15ZnO glass powder was prepared by the melt-quenching method. A copper paste containing the glass powder and formic acid-treated copper microparticles was used for metallization of α -Al 2 O 3 ceramic surface. The copper thick films were obtained by low-temperature sintering after screen printing. The effects of the glass powder contents on resistivities and shear strengths of the copper films on α -Al 2 O 3 ceramic substrate were analyzed. The microstructures of the copper thick films and the interfacial bonding mechanism on the α -Al 2 O 3 ceramic surface were investigated in detail. The copper thick film with 10-wt% 30Bi 2 O 3 –55B 2 O 3 –15ZnO glass and sintered at 650 °C for 20 min exhibited a low resistivity (3.38 ± 0.94 µΩ cm) and a high shear strength (35.24 ± 1.2 MPa). ZnAl 2 O 4 and Bi 2 B 4 O 9 were detected on the edges of the copper film near the interface, which enhanced interfacial binding between the copper thick films and the α -Al 2 O 3 ceramic substrate. These results demonstrated that the low-temperature sintering copper paste containing 30Bi 2 O 3 –55B 2 O 3 –15ZnO glass was effective for α -Al 2 O 3 ceramic surface metallization.
研究领域:
材料科学
·
陶瓷
·
冶金学
·
电子封装
✓ 已验证
DOI
高影响因子
Frontiers in Energy Research
·
2022
·
IF 3.858
Baimoldina Adel,Papadikis Konstantinos,Konysheva Elena Yu.
The incorporation of mono-sized particle catalysts in real industrial systems for biomass conversion is a significant challenge, hence the impact of individual α-Fe2O3 catalysts with varying non-ideal spherical sizes of 54 nm (FS054), 221 nm (FS221), and ∼2 µm (FSm002) as well as dual-sized mixtures (FS054-FS221 and FS221-FSm002) were considered in the catalytic upgrading of pinewood pyrolysis vapors. The size variation of the α-Fe2O3 catalyst revealed a substantial effect on the product distribution. Although the yield of phenols shows a decrease by almost a factor of two irrespective of the catalyst particle size, the FS221 catalyst demonstrates the most potent effect on reducing phenols through decarboxylation reactions. Considering the role of the catalyst on the individual phenolics, the FS221 catalyst reveals higher selectivity towards the reduction of 2-methoxyphenol, isoeugenol, and eugenol, whereas the application of FS054 catalysts displays a stronger impact on the decrease of creosol and other phenols. Both FS054 and FS221 catalysts showed the highest effectiveness in reducing the relative yield of 2-methoxy-4-vinylphenol. Applying a dual-size mixture (FS054-FS221) shows a synergetic effect, simultaneously decreasing the content of phenols, acids, and aldehydes followed by a strong CO2 release attributed to competitive decarbonylation reactions of aldehydes. The appearance of γ-Fe2O3 small fraction was revealed in the powders with mono-(FS221) and dual particle size (FS054-FS221 and FS221-FSm002), whereas the FS054 and FSm002 catalysts demonstrate good chemical and phase stability.
研究领域:
化学工程
·
材料科学
·
能源与燃料
✓ 已验证
DOI
高影响因子
MACROMOLECULES
·
2025
·
IF 5.2
Ziyuan Zhou,Binghua Wang,Changyu Shen,Bin Zhang
Previous research studies on isotactic polypropylene (iPP) have shown that the ratio of growth rate β to α phase (Gβ/Gα) exceeds 1 when the crystallization temperature (Tc) is between the lower and upper critical temperature limits (Tc** ∼ 100 °C and Tc* ∼ 141 °C, respectively), due to the faster surface kinetics of β-iPP. However, in this work, we observed that when the film thickness (d) decreases from 24 to 9 nm, the temperature interval of Gβ/Gα > 1 narrows and even disappears, as Tc* gradually shifts to lower temperatures while Tc** remains constant. This is presumably because, as d decreases, the width (wd) of the depletion zone of β-iPP expands more significantly than that of α-iPP, resulting in slower diffusion toward the growth front of β-iPP. Consequently, Gβ decreases more than Gα as d diminishes, leading to a reduction in the value of Gβ/Gα, especially at higher Tc, where Gβ/Gα becomes less than 1. Moreover, we found that the diffusion activation energy (Eaβ) of β-iPP is consistently greater than that of α-iPP (Eaα) at a given d, and the gap between Eaα and Eaβ increases as d decreases. This further highlights that the slower diffusion process for β-iPP progressively becomes the main factor affecting the difference between Gα and Gβ as d diminishes.
研究领域:
材料科学
·
高分子物理
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）