COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2023
·
IF 5.2
Chen Li,Ketong Song,Chunxiao Hao,Wanting Liang,Xiaoyun Li,Wenjin Zhang,Ying Wang,Yuefei Song
A novel anti-fouling cation exchange membrane (CEM) of sulfonated polybenzimidazole (S-PBI) was fabricated by the polymer bulk grafting modification of poly (4,4′-diphenyl ether-5,5′-bibenzimidazole) with sodium styrene sulfonate . FTIR, TGA , XPS, SEM and AFM were used to characterize membrane properties and the results showed that the ion exchange capacity and hydrophilicity of S-PBI increased with increased degrees of grafting and the electric resistance decreased accordingly. When the mass ratio of O-PBI/SSS was 1:4, the electric resistance of S-PBI-4.0 was 4.5 Ω·cm 2 , while the ion exchange capacity was 2.3 meq/g. The ED experiment with the S-PBI-4.0 membrane exhibited good desalination rate (>96 %), high current efficiency (80.73 %) and low energy consumption (1.13 kW·h/kg), which were very close to the results of a commercial CEM (Neosepta CMX). What's more, because of its good hydrophilicity, the S-PBI-4.0 membrane had better anti-fouling ability than Neosepta CMX, which was manifested as less resistance increase after membrane fouled by bovine serum albumin and smaller resistance after membrane cleaned by deionized water . These results demonstrate that the S-PBI-4.0 membrane is an appropriate candidate CEM and helpful to expand the application of ED in high-salinity organic industrial wastewater treatment .
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高影响因子
Journal of Cleaner Production
·
2022
·
IF 11.072
Xiaoman Li,Xiaolan Guo,Jiliang Niu,Jialiang Lin,Jianhua Cheng,Yongyou Hu,Yuancai Chen,Weiqiu Wen
The accumulation of antibiotics in the environment has caused worldwide concern and photocatalytic processes have shown attractive prospects for the elimination of antibiotics due to its sustainability, cleanliness and efficiency. In this study, a series of self-assembled hollow tubular Zn–In–S photocatalysts (Zn-doped In 2 S 3 , ZnIn 2 S 4 , and ZnS/ZnIn 2 S 4 ) were first designed by one-step sulfidation of Zn/In-MOFs. The as-synthesized microtubular structured Zn–In–S exhibited high surface area(107.61–127.26 m 2 /g), high porosity(0.25–0.52 cm 3 g −1 ) and high degradation rate(≥86%) towards tetracycline within 120 min. Moreover, the photoelectric properties and photocatalytic performance were dependent on the existence of Zn species. Particularly, the optimized hollow microtubular ZnS/ZnIn 2 S 4 composites exhibited ultrahigh photocatalytic degradation rate (>90%) within 1 h solar light irradiation. The kinetic constant reached 0.0379 min −1 , which was 2.96, 2.02, and 5.65 times higher than In 2 S 3 , ZnIn 2 S 4 , and ZnS respectively. The ultrahigh photocatalytic degradation efficiency originated from the formation of direct Z scheme heterojunction between ZnIn 2 S 4 and ZnS. The unique heterojunction enabled the effective separation of electron-hole pairs and the production of highly reactive oxidants (•OH, •O 2 − , h + ). Density functional theory(DFT) demonstrated a higher charge density near the Fermi level and higher affinity towards O 2 molecules, which contributed to the efficient interfacial charge mobility and O 2 activation. The work provides guidance for the modulation of ternary catalysts to maximize the virtues of photocatalytic activity .
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BIOSENSORS & BIOELECTRONICS
·
2023
·
IF 12.6
Wanru Li,Haiyan Wei,Nianlu Li,Shunyu Li,Yaru Liu,Ranran Liu,Wei Zou,Peishan Hu,Zhihu Zhang,Cuijuan Wang
Rapid detection of diquat (DQ) is essential in clinical diagnosis and rescue. Here, we developed a fast, simple-yet-practical detection strategy for the reliable identification and quantification of DQ in biological fluids. Based on surface-enhanced Raman spectroscopy (SERS), point-of-care detection was realized under the acidic condition with gold nanoparticles as the substrate. Under optimal experimental conditions, the detection limits of the strategy were 17.5 ppb and 1.99 ppm in human urine and gastric juice, respectively. High specificity and selectivity of the SERS strategy were demonstrated using common pesticides and coexisting biological substances. The method was also used to detect biofluids from 5 patients and urine samples from 10 healthy volunteers . The results were in high agreement with spectrophotometric and clinical liquid chromatography-mass spectrometry methods. The volume of urine samples required for this technique is merely 20 μL, and no preparation of the samples is required. Compared to traditional methods used in clinical settings, SERS-based methods are capable of real-time measurements that accurately provide rapid detection and response in non-laboratory settings, with great potential for on-site and point-of-care testing.
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PubMed
高影响因子
CHIRALITY
·
2023
·Vol. 35
·期 4
·247-255
·
IF 2
Yan He,Mengdi Qin,Mo Li,Defu Zhi,Baocheng Tian,Feng Qin
Flurbiprofen axetil (FA) is a prodrug of flurbiprofen (FP), and it is hydrolyzed to the active FP by carboxylesterase in plasma after intravenous injection. The pharmacological action of FP is closely related to its chirality, and S-FP shows better analgesic effects than R-FP. Therefore, it is of great significance to compare the in vivo pharmacokinetic behaviors of R-FP and S-FP. In this study, we designed a sensitive high performance liquid chromatography–tandem mass spectrometry method and used CHIRALPAK-IG3 column for chiral separation to quantify the concentrations of R-FP and S-FP in rat plasma. The results show that this method can accurately and effectively analyze the contents of R-FP and S-FP in plasma. In addition, the systemic exposure was approximately 3.09-folds for the S-FP compared with the R-FP following intravenous administration of the FA to rats at a single dose of 4.5 mg/kg. More importantly, the clearance rate of S-FP is significantly smaller than that of R-FP. Therefore, the development of S-FA injectable emulsion for clinical treatment of postoperative pain is very necessary.
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高影响因子
MOLECULES
·
2023
·Vol. 28
·期 1
·340
·
IF 4.6
Jingqi Sun,Limin Jia,Xuwei Chen
Glutathione S-transferases (GSTs) are important type-II detoxification enzymes that protect DNA and proteins from damage and are often used as protein tags for the expression of fusion proteins. In the present work, octa-aminopropyl caged polyhedral oligomeric silsesquioxane (OA–POSS) was prepared via acid-catalyzed hydrolysis of 3-aminopropyltriethoxysilane and polymerized on the surface of graphene oxide (GO) through an amidation reaction. Glutathione (GSH) was then modified to GO–POSS through a Michael addition reaction to obtain a GSH-functionalized GO–POSS composite (GPG). The structure and characteristics of the as-prepared GPG composite were characterized using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), thermogravity analysis, and surface charge analysis. The specific binding interactions between glutathione and GST gave GPG favorable adsorption selectivity towards GST, and other proteins did not affect GST adsorption. The adsorption behavior of GST on the GPG composite conformed to the Langmuir isotherm model, and the adsorption capacity of GST was high up to 364.94 mg g−1under optimal conditions. The GPG-based solid-phase adsorption process was applied to the extraction of GST from a crude enzyme solution of pig liver, and high-purity GST was obtained via SDS-PAGE identification.Keywords:octa-aminopropyl caged polyhedral oligomeric silsesquioxane (OA–POSS);graphene oxide (GO);glutathione S-transferases (GST);adsorption;solid-phase extraction
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Journal of Cleaner Production
·
2022
·
IF 11.072
Xincheng Jiang,Yanyan An,Yaoyao Huang,Wei Ding,Manli Sun,Hong Li,Huaili Zheng
The residual antibiotics in the environment will pose a threat to the environment and human health. Thus, it is imperative to develop a smart water treatment material to remove and detect antibiotics from aqueous environment simultaneously. In this study, magnetic Cu–Ni–S@Ni foam was synthesized by liquid phase vulcanization method to in-situ load Cu–Ni–S nanostructures on the surface of Ni foam. The novelty of this material is the combination of adsorption-flocculation technology and semi-quantitative detection technology. Batch experiments showed that Cu–Ni–S@Ni foam has a high removal rate of norfloxacin (NOR) (96.92%), wide pH adaptability (pH = 4.0–10.0) and strong ion interference resistance (0.1–100 mmol/L). According to the Langmuir isotherm , the removal capacity can reach 417.4 mg/g at 25 °C, which is much higher than that of other water treatment agents reported in most studies. Characterization analysis indicated that the main removal mechanisms are surface complexation, cation bridging, electrostatic attraction , precipitation and flocculation . Transmission FTIR detection experiments showed that NOR on Cu–Ni–S@Ni foam has easily recognizable FTIR fingerprints; the intensity of characteristic peaks roughly reflects the concentration information of NOR to some extent. This semi-quantitative detection method, requiring simple operation without the fabrication of KBr tablet, has a wide linear range (5–100 mg/L) and a low limit of detection (4.6 mg/L). Therefore, Cu–Ni–S@Ni foam can be used for simultaneous removal and semi-quantitative detection of NOR in wastewater. It has potential application value in wastewater treatment and water quality monitoring.
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高影响因子
JOURNAL OF THE EUROPEAN CERAMIC SOCIETY
·
2022
·
IF 6.364
Zexuan Sui,Yan Sun,Yue Jing,Ci Wang,Yao Zhu,Sen Qian,Jing Ren,Jianzhong Zhang
We report the first study on in-situ co-growth of biphasic CsPbBr 3 and Zn-Cd-S quantum dots (QDs) in borosilicate glass , and provide explicitly evidence of their morphology and nanoscale distribution. Such biphasic QDs co-doped nano-glass composites show unique green and red dual-band emissions. By changing the thermal heating scheme, the fluorescence intensity ratio (FIR) and thus the apparent color can be widely adjusted. The FIR can be also fine-tuned simply by varying the excitation wavelength. Based on the FIR, a self-calibrated X-rays dosimeter is constructed, which also possesses a good thermal stability. Although the X-rays induced scintillation weakening occurs, it can be readily recovered by post-thermal-annealing.
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Catalysis Science & Technology
·
2023
·Vol. 13
·期 3
·898-909
·
IF 5
Haohui Gu,Feng Liang,Xiaohan Wang,Shuaibing Wu,Gongye Lv,Haijun Zhang,Shaowei Zhang,Lilin Lu,Zhijun Dong
The design of heterojunction photocatalysts is regarded as a very effective method to solve the high recombination rate of photogenerated charge carriers for CO2 photoreduction into hydrocarbons, and interface engineering is urgently required to achieve high efficiency. Herein, graphitic carbon nitride (g-C3N4, CN) was uniformly grown on the surface of nitrogen-doped rutile TiO2 (NT) nanorods by in situ deposition, and a NT@CN core/shell step-scheme (S-scheme) heterojunction system composed of NT nanorods and g-C3N4 was synthesised. The as-synthesised heterojunction containing 55 wt% g-C3N4 delivered the highest CO2 photoreduction activity (33.35 μmol g−1 for CO) without additional cocatalysts or external sacrificial agents, which was 7.1 times higher than that of bare NT nanorods. This improved CO2 reduction activity was attributable to the large surface area and impactful S-scheme heterostructure, which imparted the catalyst with sufficient visible-light harvesting ability, promoted the segregation and transformation of the photoinduced charge pairs, and enhanced the redox ability of the carriers. Concurrently, the NT@CN photocatalyst exhibited excellent reusability and stability. This work offers a new basis for designing and preparing rutile TiO2-based S-scheme heterojunctions with enhanced CO2 reduction performance.
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2023
·
IF 4.5
Fangfang Shi,Zhengchu Zhang,Yongjie Xu,Chao Yang,Jianhui Qiu,Jiachi Liao,Limin Zang
Developing sustainable carbon materials from biomass for supercapacitors is a promising solution to alleviate energy and environmental pressures. In this paper, novel N/S co-doped carbon nanosheets derived from sugarcane processing by-products are proposed. Flexible and binder-free electrodes based on carbon felt and sulfonated potassium fulvic acid were prepared by a simple impregnation-carbonization method. The maximum areal specific capacitance, power density and energy density of the symmetric supercapacitor are 409.9 mF cm −2 (1 mA cm −2 ), 0.92 mW cm −2 and 184.5 μWh cm −2 , respectively. The operating voltage of the device increases to 1.8 V by using LiCl electrolyte. After 10,000 cycles, the capacitance remains 90 % of its initial value. Besides, the device possesses good flexibility, which can be bent at different angles and has a capacitance retention of 92.3 % after 5000 bending cycles. The supercapacitor is of great significance for the recovery of crop processing by-products to prepare flexible electronic devices.
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高影响因子
NEW JOURNAL OF CHEMISTRY
·
2023
·Vol. 47
·期 8
·3745-3757
·
IF 3.3
Litao Jia,Pei Yu,Ying Dong,Yonglei Xing,Juan Peng,Gang Ni,Xiaoyong Jin
The decomposition efficiency of refractory organic pollutants depends strongly on the characteristics of the photoanode semiconductors in the photoelectrocatalytic (PEC) process. The selection of superior materials with excellent PEC efficiency is a challenge in the practical application of PEC oxidation technology. Herein, a novel S-Co3O4/Bi2WO6 heterojunction photoanode was fabricated using a simple hydrothermal procedure. Compared with Bi2WO6 nanoflowers, the as-prepared S-Co3O4/Bi2WO6 photoanode had a large electroactive surface area, low charge transfer resistance, strong light absorption ability, and high separation efficiency for induced photogenerated electron/hole pairs (e−/h+). This relies on the fact that S doping not only controls the morphology of Co3O4 but also changes its intrinsic electronic structure to improve the interlayer polarization. Notably, the Z-scheme heterojunction formed by the combination of S-Co3O4 and Bi2WO6 not only enhances the e−/h+ separation efficiency but also results in a stronger redox ability than that of pure Bi2WO6. In addition, reactive species trapping experiments and electron spin resonance tests demonstrated that the S-Co3O4/Bi2WO6 photoanode plays a dominant role in the degradation of tetracycline (TC) by ˙O2− and ˙OH radicals. Therefore, the prepared S-Co3O4/Bi2WO6 photoanode exhibits better PEC performance than Co3O4, S-Co3O4 and Bi2WO6 in the degradation of TC. The optimized S-Co3O4/Bi2WO6 composite showed a degradation rate of 87.4% in 30 mg L−1 TC solution. This work provides a new strategy for the construction of efficient photoelectroanodes.
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Small
·
2023
·
IF 13.3
Pengpeng Jia,Yu Zou,Jiang Jiang
Development of wound dressing with robust antibacterial and repair-promoting activity has always been an urgent biomedical task during the past years. The therapeutic effect of current hydrogel dressings containing single bioactive agent like nanoparticle or gas is still unsatisfactory for the treatment of infected wound. Herein, a CuS/NO co-loaded hydrogel (CuS/NO Gel) is proposed, which is constructed by sequential polymerization, reduction, and S-nitrosylation of CuS hybrid hydrogel with disulfide bonds. These CuS/NO Gel patches show good mechanical stability, high photothermal activity and excellent biocompatibility. When being applied to treat infected wound, CuS/NO Gel can not only eliminate infection effectively by the synergistic effect of mild photothermal heating and boosted NO release in infection phase, but also promote vascularization and collagen deposition due to the synchronous supply of Cu ion nutrients and low concentration NO signaling molecules in wound repair phase. Compared to hydrogel dressings with individual active agent (CuS Gel or NO Gel), CuS/NO Gel exhibits better antibacterial and repair-promoting activity both in vitro and in vivo. Therefore, this CuS/NO Gel holds great promise in the future clinical treatment against infected wound.
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高影响因子
RSC Advances
·
2023
·Vol. 13
·期 50
·35689-35694
·
IF 3.9
Huandi Hou,Ting Wang,Baohuan Wang,Wenting Guo,Xiang Miao,Xin Liang
Co–Mo–S based catalysts have promising applications in both the hydrogen evolution reaction (HER) and hydrodesulfurization (HDS). Herein, Co–Mo–S catalyst and Co–Mo–S catalyst with and without NaBH4 modification have been successfully synthesized by a simple hydrothermal synthesis method. Co–Mo–S catalysts with NaBH4 modification show better catalytic activity towards both HDS and the HER. The phase purity, morphology, crystal structures and electron valence distribution of the catalysts with and without NaBH4 modification were studied by experimental characterizations and theoretical calculations. The catalysts without NaBH4 modification are mostly 2H-MoS2, while the catalysts without NaBH4 modification have 1T-MoS2, and 1T-MoS2 is exposed to more active sites, which will be conducive to the results of HDS performance of the catalyst. DFT calculations investigated the required activation energies of 1T-MoS2 and 2H-MoS2 for HDS and HER, respectively. The activation energy required for both HDS and H2 generation of 1T-MoS2 is significantly lower than that for the 2H-MoS2 structure.
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高影响因子