BIOCONJUGATE CHEMISTRY
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2021
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IF 4.774
Chunxiao Sui,Rui Tan,Yiwen Chen,Guotao Yin,Ziyang Wang,Wengui Xu,Xiaofeng Li
Metal–organic frameworks (MOFs) derivatives had been widely explored in electronic and environmental fields, but rarely evaluated in the biomedical applications. Herein, Fe–N codoped carbon (FeNC) nanoparticles were synthesized and characterized via facile pyrolysis of precursor ZIF-8 (Fe/Zn) nanoparticles, and their potential applications in tumor therapy were assessed in this investigation both in vitro and in vivo. After PAA (sodium polyacrylate) modification, the FeNC@PAA nanoparticles were able to initiate a Fe-based Fenton-like reaction to generate ·OH and O2 for chemodynamic therapy (CDT) and O2 evolution. Meanwhile, the porphyrin-like metal center in the FeNC@PAA nanoparticles could be used as a photosensitizer for photodynamic therapy (PDT) of tumors, which could be enhanced by O2 generated in CDT. Furthermore, the FeNC@PAA nanoparticles were also found to be effective in photothermal therapy (PTT) with a photothermal conversion efficiency of 29.15%, owing to a high absorbance in the near-infrared region (NIR). In conclusion, the synthesized FeNC@PAA nanoparticles exhibited promising applications in O2 evolution and CDT/PDT/PTT synergistic treatment of tumors.
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高影响因子
CORROSION SCIENCE
·
2020
·
IF 6.479
Junying Hu,Qi Xiong,Longjun Chen,Chenfeng Zhang,Ziqi Zheng,Shuai Geng,Zhi Yang,Xiankang Zhong
The corrosion inhibition of carbon steel in CO 2 -O 2 -containing environment is one of the biggest challenges in flue gas injection for enhanced oil recovery. Herein we report the possibility to use Bis(2-ehylhexyl) phosphate (BEP) to inhibit the corrosion in CO 2 -O 2 -containing solution and simultaneously the inhibition mechanisms are unmasked. The results show that the corrosion is greatly inhibited with 500 ppm BEP in 1 wt% NaCl solution with 0.02 MPa CO 2 and 3 mg/L O 2 . BEP could interact with Fe and corrosion products via the formation of P-O-Fe bond and P-Fe bond to generate a barrier layer, thus, offering a protective performance.
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JOURNAL OF POWER SOURCES
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2020
·
IF 8.247
Ying Wang,Dan Li,Siqi Zhang,Ziye Kang,Haiming Xie,Jia Liu
Although dual redox mediators (RMs) largely promote the discharge capacity and decreases the charge overpotential in Li-O 2 batteries , the shuttle effect leads to a RM degradation and a serious deterioration of Li metal, which results in a poor sustainability. Here, a poly (3,4-ethylenedioxythiophene):poly (styrenesulfonate) (PEDOT:PSS) -decorated separator has been firstly introduced into a dual mixture RMs-involved Li-O 2 system, which restrains the shuttle effect via coulombic interactions. Benefiting from the advantages of as-prepared separator, a cell exhibits an enhanced cycling stability and a good reversibility associated with the Li 2 O 2 formation and decomposition during cell cycling. These results represent a promising progress in the development of an easy-to-operate modified separator for a highly efficient Li-O 2 battery.
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SCIENCE OF THE TOTAL ENVIRONMENT
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2018
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IF 4.61
Sharafat Ali,Izaz Ali Shah,Aziz Ahmad,Javed Nawab,Haiou Huang
In this study, pristine multi-walled carbon nanotubes (MWCNTs) were functionalized by using Ar/O 2 plasma treatment technique, which enhanced adsorptive membrane filtration of zinc ions from water and wastewater. The XPS analysis showed that plasma treatment largely increased the surface oxygen groups content of MWCNTs from 2.78% to 6.79%. This change increased the surface negative charged, dispersion and adsorption properties of MWCNTs without causing any damages to the integrity of the nanotube pattern. Pressure-driven filtration of plasma-treated MWCNT (P-CNT) dispersion formed a stable layer inside the lumen of a hollow fiber membrane. The contact angle analysis demonstrated that after incorporation of P-CNT into the HF membrane increased membrane hydrophilicity. The P-CNT membrane effectively removed almost 100% of zinc from synthetic waters and approximately 80% of zinc from a wastewater effluent by surface complexation reaction. A follow-up regeneration study demonstrated that the adsorptive removal of zinc by the CNT membrane was reversible under selected conditions, thus making it possible to repeatedly use the membrane for long-term zinc filtration. This study suggests that HF membranes modified with P-CNTs possess superb adsorption properties for metal ions , allowing the operation of CNT membranes for water treatment .
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CHEMICAL ENGINEERING JOURNAL
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2013
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IF 3.473
Xiaofeng Xu,Peng Liao,Songhu Yuan,Man Tong,Mingsen Luo,Wenjing Xie
A novel Pd-based electro-Fenton process has recently been developed to degrade organic contaminants in wastewaters and groundwater. However, the high cost of Pd catalyst limits the application of this process. In this study, Cu supported on bamboo charcoal (Cu/C) was synthesized to evaluate the feasibility of substituting Pd catalysts. Using phenol as a probe organic contaminant, the performance of Cu/C catalyst was evaluated for the electro-Fenton degradation of phenol in a typical undivided electrolytic system. The electrochemical degradation of phenol in the presence of Cu/C was significant, following a pseudo-first-order kinetics with rate constant ( k 1 ) of 0.008 min −1 . The addition of Fe 2+ remarkably enhanced the degradation ( k 1 = 0.012 min −1 ). H 2 O 2 and OH were validated as the reactive oxidizing species (ROSs), and OH was the main ROS contributing to phenol degradation. The as-synthesized Cu/C consisting of Cu, CuO and Cu 2 O could catalyze the production of H 2 O 2 from chemisorbed H 2 and O 2 as well as the decomposition of H 2 O 2 to OH. Particularly, the addition of Fe 2+ facilitated the transformation of H 2 O 2 to OH. Phenol degradation increased with increasing the current from 5 to 50 mA and decreased with the further increase to 100 mA. The degradation improved with the increase in Cu loadings and the decrease in solution pH. The presence of NaNO 3 , Na 2 SO 3 or Na 2 S inhibited the degradation, while the presence of NaCl increased the degradation. Although the activity of Cu/C is much lower than that of Pd/C for phenol degradation, the cost of Cu/C is much lower.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2025
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IF 9
Yunxiang Bai,Xinxue Qiu,Deqiang Chen,Junwei Zheng,Liangliang Dong,Chunfang Zhang
Magnetic mixed matrix membranes (MMMs) show great potential for enhancing O 2 /N 2 separation efficiency by leveraging the inherent magnetic property differences between O 2 (paramagnetic) and N 2 (diamagnetic). However, one of the major challenges is the establishment and precise control of magnetic channels between magnetic fillers and polymer matrix. To address this issue, herein, ZIF-8 wrapped Fe 3 O 4 nanoparticles (Fe 3 O 4 @ZIF-8) were synthesized using a step-by-step assembly method, and then integrated into polymer of intrinsic microporosity (PIM-1) matrix to develop MMMs with well-defined magnetic channels for O 2 /N 2 separation. In comparison with Fe 3 O 4 , Fe 3 O 4 @ZIF-8 nanoparticles exhibited significantly enhanced compatibility with the polymer matrix, thereby facilitating uniform dispersion and improving interfacial adhesion. Gas permeation experiments revealed that the magnetic PIM-1/Fe 3 O 4 @ZIF-8 MMMs demonstrated enhanced O 2 /N 2 separation performance due to the combined effects of magnetic responsiveness and the presence of ZIF-8 magnetic channels. Under a magnetic field strength of 56mT, the magnetic MMM with a 4 wt% loading of Fe 3 O 4 @ZIF-8 exhibited optimal O 2 /N 2 separation performance with O 2 permeability of 710 Barrer and O 2 /N 2 selectivity of 3.64. These values represented a significant improvement of 42% and 24%, respectively, compared to pure PIM-1 membrane. Moreover, the simultaneous improvement of permeability and selectivity enabled the achievement of Robeson’s 2008 upper bound for O 2 /N 2 separation, underscoring the great potential of Fe 3 O 4 @ZIF-8 nanoparticles for designing magnetic MMMs with favorable structural attributes and exceptional separation efficiency.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2024
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IF 9.4
Shengqi Ding,Liang Wu,Xianxia Yuan
Electrocatalysts with appropriate electron coupling toward LiO 2 intermediates can exhibit superior oxygen reduction/evolution reaction kinetics in Li-O 2 batteries (LOBs). In this work, a charge redistribution strategy has been developed by constructing NiS/MoS 2 heterostructure nanosheet self-assembled hollow microspheres with an internal electric field to regulate the interaction with LiO 2 and then improve the electrochemical performance of LOBs. Density functional theory calculations and physicochemical characterizations reveal that the difference of work functions between NiS and MoS 2 promotes the electron redistribution in heterointerface via built-in electrical field, leading to increased electron density of interfacial Ni atom, thereby enhancing its electron coupling toward LiO 2 intermediates and promoting one-electron oxygen reduction/oxidation reaction kinetics. As a result, the NiS/MoS 2 -based LOBs exhibit evidently higher discharge capacity and much better cycling performance than the batteries using NiS and MoS 2 . This work provides a reliable charge redistribution strategy induced by build-in electric field to design efficient catalysts for LOBs.
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Small
·
2024
·
IF 13
Qixin Shi,Yingqun Nian,Yang You,Ziyan Li,Yunqi Li,Ran Zhao,Zhengzhi Chen,Tianhang Huang,Bing Hu
Edible bioplastics offer a possible approach with great potential to address the challenges of plastic and microplastic crisis and the issue of food waste. In the present study, in situ, induction of fibrillation of legume proteins within chitosan matrix is found to form edible bioplastic films with a high CO 2 /O 2 selectivity coefficient of ≈130. Desirable mechanical properties, including a high elongation at break of ≈230%, are realized to fabricate shopping bags, which can be filled with 5 kg of fruits. An atmosphere with a high CO 2 content and low O 2 concentration is spontaneously achieved after strawberries are packaged with the films and ≈85% of the fruits are edible after 9 days. The contents of CO 2 in the equilibrium state and the percent of edible fruits are positively correlated with the CO 2 /O 2 selectivity of the films. By comparison of the edible bioplastic films made from mung bean protein (MP) and pea protein (PP), the fibrillation capability of legume proteins and the heterogeneity in polydisperse diameters of the protein fibrils and chitosan are demonstrated to make great contributions to the dense microstructure, leading to the strong mechanical properties and high gas selectivity of the films. The structure-property relationship is elucidated for high-performance bioplastics films.
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JOURNAL OF THE EUROPEAN CERAMIC SOCIETY
·
2024
·
IF 5.8
Bei Ren,Ziqian Meng,Bixian Zhang,Sihao Jian,Chufei Cheng,Jiadong Hou,Ruixin Hao,Bo Li,Yang Miao,Chao Ma,Weihua Ji
High-entropy fluorite oxide ceramics are promising candidates for spacecraft applications due to their excellent high-temperature thermal-mechanical properties. In this work, four kinds of high-entropy fluorite oxide ceramics ((ZrHfCeYEr) (1-x)/5 Ti x )O 2-δ (HEFOs, x = 0, 0.025, 0.05, 0.075) with different Ti 4+ contents were successfully synthesized through solid-state reaction method with conventional sintering. They all exhibited phase stability when annealed at 1500 ℃ for 20 h. When the content of Ti 4+ was increased to x = 0.075, the thermal conductivity reduced to1.34 W·m −1 ·K −1 at 1100 ℃, and the hardness and elastic modulus increased to 14.01 GPa and 205.70 GPa, respectively. Furthermore, the cyclic thermal shock resistance of HEFOs at different temperatures was investigated. The initial flexural strength reached 219.03 MPa when the content of Ti 4+ was increased to x = 0.075. After 60 thermal shock cycles at 1200 ℃ and 1500 ℃, the residual strength ratios were 97.56 % and 83.36 %, respectively. The results of this study establish the foundation for future applications of high-entropy fluorite oxide ceramics in spacecraft hot-end components.
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高影响因子
JOURNAL OF CATALYSIS
·
2024
·
IF 6.5
Ruoyuan Li,Aixia Li,Junhua Li,Yao Wang,Zhiming Liu
Selective catalytic reduction of NO x by CO (CO-SCR) in the presence of O 2 is challenging because in this process CO is prone to being oxidized by O 2 , thus inhibiting NO x reduction by CO. Furthermore, SO 2 typically leads to the deactivation of the CO-SCR catalyst. Herein, a significant promoting effect of SO 2 on Ir/SiO 2 catalyst for the CO-SCR of NO x in the presence of O 2 is reported. In-situ X-ray Absorption Fine Structure (XAFS) and X-ray photoelectron spectroscopy (XPS) analysis showed that SO 2 does not affect the chemical nature of Ir 0 under reaction conditions. However, SO 2 can be oxidized to sulfate and deposit on the catalyst surface. In situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) analysis demonstrated that the presence of SO 2 can inhibit the CO + O 2 reaction, thus leaving more CO available to reduce NO x over the active Ir 0 sites. As a result, the reduction of NO x is remarkably promoted even in the presence of O 2 and SO 2 .
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Catalysis Science & Technology
·
2020
·Vol. 10
·期 21
·7378-7385
·
IF 5.721
Mengna Ding,Fengyan Shi,Huijuan Zhu,Yuping Yang,Jiahui Zhong,Liulin Luo,Yuning Huo,Hexing Li
A hybrid Cu2O/TiO2 composite loaded on a Cu mesh (Cu2O/TiO2@Cu mesh) was developed via a supercritical solvothermal route. A uniformly distributed Cu2O/TiO2 p–n hetero-junction was stably coated on a Cu mesh, benefiting the visible-light harvesting. In comparison to electrochemistry and visible-light photocatalysis, the photoelectrochemistry process on the photoanode of the Cu2O/TiO2@Cu mesh presented improved bacterial inactivation activity for Acinetobacter baumannii. By means of the main active species of ˙O2− radicals, the photoelectrocatalytic process on the Cu2O/TiO2@Cu mesh also realized complete leakage of K+ ions, much stronger mineralization of the cell membrane and more efficient elimination of the self-recovery function, finally leading to cell death. In comparison, the electrochemistry process only led to the leakage of K+ ions without inactivation of bacteria, and the visible-light photocatalysis process induced partial leakage of K+ ions and cell mineralization after the death of most bacteria.
研究领域:
环境科学
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材料科学
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微生物学
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光电催化
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ENVIRONMENTAL SCIENCE & TECHNOLOGY
·
2025
·
IF 11.3
Hao Liu,Siqing Cheng,Jianjun Chen,Xiaoping Chen,Shangchao Xiong,Fang Huang,Houfeng Liu,Junhua Li,Chuanzhi Sun
Mitigating industrial nitrous oxide (N2O) emissions is critical for climate action, yet developing efficient low-temperature N2O decomposition catalysts under O2-containing conditions remains challenging. The weak oxygen–support interaction leads to unsatisfactory N2O decomposition performance in the supported Co3O4/CeO2 catalyst. This study aims to enhance the electronic oxide–support interaction in the Co3O4/CeO2 catalyst through Zn doping, thereby improving its catalytic performance for N2O decomposition under O2-rich conditions. The results demonstrate that, in the presence of 5% O2, the activation energy of the catalyst sharply decreases from 117.5 to 60.4 kJ·mol–1 after Zn doping (Co2.4Zn0.6O4/CeO2). Additionally, the doped catalyst exhibits strong durability to the O2 + H2O + NOx impurity gas components. Advanced spectral characterization and density functional theory calculations reveal that Zn doping modulates the geometry and electronic structure of active cobalt sites, optimizing the adsorption and activation capabilities of N2O molecules. This study elucidates the mechanism of N2O decomposition over the catalysts and establishes a clear structure–activity relationship between the atomic-scale configuration of active sites and their performance. These findings provide critical insights for designing efficient supported oxide catalysts through targeted doping strategies and offer new perspectives for developing highly efficient and low-energy N2O decomposition catalysts.
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