JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2022
·
IF 9.965
Qian Wang,Weiwang Qiu,Mengna Li,Na Li,Xiaoran Li,Xiaohong Qin,Xueli Wang,Jianyong Yu,Faxue Li,Liqian Huang,Dequn Wu
Diabetic wound treatment remains a major challenge due to the difficulties of eliminating bacterial biofilm and relieving wound hypoxia . To address these issues simultaneously, a multifunctional Dex-SA-AEMA/MnO 2 /PDA (DSAMP) hydrogel platform was developed with excellent biocompatibility and porous structure. The hydrogel could absorb the exudate, maintain humidity and permeate oxygen, which was prepared by encapsulating polydopamine (PDA) and manganese dioxide (MnO 2 ) into Dex-SA-AEMA (DSA) hydrogel by UV irradiation . With the addition of PDA , the DSAMP hydrogel was proved to eliminate the biofilm after NIR photodynamic therapy (PTT, 808 nm) irradiation at 54 °C. Furthermore, in order to mitigate hypoxia wound microenvironment, MnO 2 nanoparticles were added to convert the endogenous hydrogen peroxide (H 2 O 2 ) into oxygen (O 2 , 16 mg L −1 ). The diabetic wound in vivo treated by DSAMP hydrogel was completely healed on 14 days. It was revealed that the DSAMP hydrogel possessed a great potential as dressing for diabetic chronic wound healing.
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BIOELECTROCHEMISTRY
·
2022
·
IF 5.76
Yanjing Yun,Zhisong Lu,Xiaodan Jiao,Peng Xue,Wei Sun,Yan Qiao,Yang Liu
Relationship between mycotoxin-induced hormesis and reactive oxygen species (ROS) has not been systematically investigated due to the lack of an effective analysis method. To monitor cellular release and intracellular level of O 2 ·− , carboxymethyl cellulose-Mn 3 (PO 4 ) 2 nanocomposite was synthesized to fabricate an electrochemical biosensor, which selectively detects O 2 ·− over the range of 57.50 nM ∼ 2.95 μM (R 2 = 0.99) with the sensitivity of 78.67 μA μM −1 cm −2 and the detection limit of 8.47 nM. Transient exposure to zearalenone (ZEA) induces the enhancement on cell viability, immediate O 2 ·− release from cells, and reduction of intracellular O 2 ·− level. After post-treatment culture, intracellular O 2 ·− initially increases to a high level and then decreases to the normal level. Concurrently, the ZEA-induced hormesis disappears. Based on the findings, we propose a mechanism, involving the ROS release, increase of succinate dehydrogenase activity and recovery of intracellular ROS, to explain the occurrence and disappearance of hormesis in intestinal porcine enterocytes.
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JOURNAL OF MEMBRANE SCIENCE
·
2023
·
IF 9.5
Hongyong Zhao,Ting Song,Xiaoli Ding,Ruyi Cai,Xiaoyao Tan,Yuzhong Zhang
Membrane technology for O 2 /N 2 separation is a mature industrial unit. Membranes with excellent permeation-separation performance are still one of the critical requirements. The cobalt-based compounds have been well known for their good affinity for O 2 , which can facilitate O 2 transfer and improve the O 2 /N 2 selectivity in membranes. The cobalt-based compounds, moreover, have a magnetic responsive effect, which can lead to a further improvement in O 2 /N 2 separation under a magnetic field. A class of PIM-1 mixed matrix membranes (MMMs), containing cobalt-based ionic liquid (CILs)@polyarylate (aromatic polyester) (PAR) (core-shell) composite nanospheres (CILs@PAR (c-s) CNPs), were prepared. Chemical compositions of CILs@PAR (core-shell) CNPs were determined by Fourier transform infrared spectroscopy (FTIR). Morphologies and structures of CILs@PAR (core-shell) CNPs were observed by transmission electron microscopy (TEM). Gas adsorption properties of CILs@PAR (core-shell) CNPs were tested. Thermal properties of the (CILs@PAR (c-s) CNPs)/PIM MMMs were investigated by simultaneous thermal analysis (TGA-DSC). Gas permeation-separation performances of the (CILs@PAR (c-s) CNPs)/PIM MMMs were also reported. Compared with the original PIM-1 membrane, the (CILs@PAR (c-s) CNPs)/PIM MMMs display higher O 2 /N 2 selectivity because of cobalt-based ionic liquid as O 2 carrier, coupled with a reduction in O 2 permeability. With increasing the content of the CILs@PAR (c-s) CNPs, the O 2 /N 2 selectivity increases, and the O 2 permeability decreases. It is also found that, as a magnetic field on the MMMs, the O 2 /N 2 selectivity further increases; and it increases more, as a higher content of CILs@PAR (c-s) CNPs. Therefore, the (CILs@PAR (c-s) CNPs)/PIM MMMs exhibit excellent O 2 /N 2 selectivity of ∼5 coupled with good O 2 permeability of ∼140 Barrer under a 180 mT magnetic field and show great potential for air separation.
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CERAMICS INTERNATIONAL
·
2023
·
IF 5.2
Siyuan Li,Cuiwei Li,Huaiming Jia,Guangjin Chen,Kepi Chen,Linan An
In this paper, a series of (Ce 0.2 Zr 0.2 Ti 0.2 Sn 0.2 Y 0.2- x Ca x )O 2-δ ( x = 0∼0.2) high-entropy of compositionally-complex ceramics were prepared using solid-state reaction method. The results showed that the content of Ca 2+ had significant effects on the phase composition, microstructure and properties of the prepared materials. As Ca 2+ content increased, single-phase fluorite was easier to form. When x ≤ 0.05, materials contained dual-phase of fluorite and pyrochlore structures. When x ≥ 0.075, the prepared materials showed single-phase fluorite structure, which indicated that high-entropy fluorite ceramics (HEFCs) could be prepared under this condition. When Ca 2+ content increased from 0.075 to 0.2, grain size of HEFCs decreased, and relative density decreased from 95.7 % to 78.6 %. Thermal conductivity of these HEFCs varied from 1.87 W m −1 K −1 to 1.60 W m −1 K −1 , which was lower than 8YSZ. As Ca 2+ content increased, both size disorder and mass disorder increased too leading to low thermal conductivity. The results indicate that the prepared HEFCs are promising for thermal insulation applications.
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CHEMOSPHERE
·
2021
·
IF 7.086
Wei Zhou,Xiaoxiao Meng,Jihui Gao,Fei Sun,Guangbo Zhao
s Hydrogen peroxide (H 2 O 2 ) electrosynthesis from 2-electron O 2 reduction reaction (2eORR) is widely regarded as a promising alternative to the current industry-dominant anthraquinone process. Design and fabrication of effective, low-cost carbon-based electrodes is one of the priorities. Many previous work well confirmed that hydrophilic carbon-based electrodes are preferable for 2eORR. Here, we proposed a strategy of hydrophilicity-hydrophobicity regulation. By using commercially available graphite felt (GF) as electrodes, we showed that both hydrophilic GF, hydrophobic GF, and Janus GF yielded significantly higher H 2 O 2 production, which is 7.3 times, 7.6 times, and 7.7 times higher than the original GF, respectively. Results showed that currents and stirring rates affect the H 2 O 2 yields. The enhancement of hydrophilic GF is due to the incorporation of oxygen-containing functional groups, while the hydrophobic and Janus GF comes from the locally confined O 2 bubbles, which built a gas-liquid-solid interface inside GF and thus enhance the H 2 O 2 formation kinetics. Finally, the effectiveness of the hydrophilicity-hydrophobicity regulation concept was tested in Electro-Fenton process by removing typical dyes and antibiotics. This work supply an effective but facile strategy to enhance the performance of carbon-based electrodes towards 2eORR by regulating the micro-environment of electrodes.
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ACS Catalysis
·
2020
·
IF 12.35
Mo Zhang,Zheng Li,Xing Xin,Junhao Zhang,Yeqin Feng,Hongjin Lv
Selective production of value-added platform chemicals from renewable biomass feedstocks and their derivatives has attracted tremendous attention with high potential in addressing global problems of energy and sustainability. In this work, a lead-halide perovskite (MAPbBr3, MA = methylammonium) is utilized as a photocatalyst for selective oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-diformylfuran (DFF) using atmospheric O2 upon visible-light irradiation. Under minimally optimized conditions, the photocatalytic conversion of HMF in acetonitrile solvent reaches 100% with a DFF selectivity of over 90%, achieving an overall furanic carbon yield of over 96%. A detailed catalytic mechanism was proposed based on various spectroscopic and experimental results, revealing that the atmospheric O2, photogenerated electrons (e–), holes (h+), •O2–, and 1O2 species together play crucial roles in the effective and selective photo-oxidation of HMF to DFF. In addition, our present photocatalytic system is also applicable for photo-oxidation of benzyl alcohol with approximately 100% conversion and benzaldehyde selectivity, providing insights for future exploration of the present catalytic system.
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ELECTROCHIMICA ACTA
·
2020
·
IF 6.215
Mingjie Sun,Shuai Guo,Ziling Wang,Lu Zou,Bo Chi,Jian Pu,Jian Li
It is crucial to design effective cathode catalysts for high performance of Li–O 2 batteries (LOBs). Herein, porous LaCo 0.6 Ni 0.4 O 3 nanofibers decorated with ultrafine Co 3 O 4 nanoparticles (Co 3 O 4 @LCN NFs) are designed and employed as cathode catalyst for LOBs. The X-ray photoelectron spectroscopy measurement results suggested that uniform dispreading of Co 3 O 4 nanoparticles on LCN NFs surface could largely increase the surface chemisorbed oxygen, resulting in enhanced catalytic activity. Furthermore, with the assistance of Co 3 O 4 nanoparticles, Co 3 O 4 @LCN NFs can significantly facilitate O 2 adsorption and diffusion, Li 2 O 2 nucleation/decomposition and the formation of tiny sheet-like Li 2 O 2 , thereby achieving a low charge overpotential. A high specific capacity of 11,288 mA h g −1 , a low charge voltage plateau of 3.72 V at first cycle and excellent cycle stability of 116 cycles at 1000 mA g −1 are obtained for LOBs with Co 3 O 4 @LCN NFs.
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2020
·
IF 16.683
Yanbin Wang,Di Meng,Xu Zhao
Visible-light-driven H 2 O 2 production from O 2 reduction is an eco-friendly strategy and attracts increasing attentions. In this study, KOH modified graphitic carbon nitrides (CNKx) were constructed through the thermolysis of melamine-cyanuric acid supramolecular-complex in the presence of KOH. The BET specific surface area of CNK 0.2 with porous structure was 92 m 2 g −1 . The photocatalyst was characterized by XPS, ESR and element analysis and the analysis suggested that nitrogen vacancy was created in the framework of g-C 3 N 4 . Photoluminescence (PL) spectra indicated that the recombination of photogenerated electrons and holes was efficiently suppressed. ζ-potential revealed that more negative charge on the surface of CNK 0.2 , which promoted the adsorption of O 2 and accelerated the photocatalytic H 2 O 2 production. ESR experimental and radical quenching results illustrated that superoxide radical (O 2 - ) was the primary intermediate during the O 2 reduction process, suggesting the O 2 reduction pathway by CNK 0.2 was the sequential two-step single-electron reduction.
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ACS Omega
·
2021
·
IF 3.512
Shuangping Xu,Wenqiang Ma,Hailiang Zhou,Yushu Zhang,Hongge Jia,Jingyu Xu,Pengfei Jiang,Xintian Wang,Wenwen Zhao
The synthesis of poly(methyhydrosiloxane) (PMHS) and N,N′-bis(3-allyl)pyromellitic diimide was optimized for O2/N2 separation. The membrane exhibits excellent mechanical and thermal properties and shows an O2/N2 selectivity of up to 4.44 with an O2 permeability of 31.0 Barrer; compared with polydimethylsiloxane (PDMS) and pure polyimide (PI) membranes, the separation selectivity shows a 107% increase for PDMS, and the permeation shows a 660% increase for pure PI. The obtained results were well above the ones reported on the literature for similar conditions opening the door for the preparation of a stable polysiloxane (PMHS-I) gas separation membrane with extraordinary O2/N2 separation performance.
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CHEMICAL ENGINEERING JOURNAL
·
2021
·
IF 13.273
Lehui Ren,Mei Chen,Jinxing Ma,Yang Li,Zhiwei Wang
In this study, a novel reactive electrochemical membrane (REM) made of Pd-loaded porous Ti was prepared to achieve ultrafast and efficient oxidation of trace antibiotics sulfamethoxazole (SMX) under anodic polarization. At a current density of 0.5 mA/cm 2 , the percentage removal of SMX by the REM was 96.3% in flow-through mode, with the energy cost ( i.e. , the electrical energy per order of removal, 1.34 Wh/m 3 ) being much lower than the flow-by mode (125.76 Wh/m 3 ) under the same operating condition. Quenching experiments and electron spin resonance spectra demonstrated that singlet oxygen ( 1 O 2 ) was the main reactive oxygen species in the REM system, playing a vital role in SMX degradation. Results of this study indicated that 1 O 2 was mainly generated on the anode via Pd–O 2 interaction that directly activated oxygen, rather than the evolution of 1 O 2 precursors ( e.g ., O 2 − and H 2 O 2 ). The constantly high electrochemical removal of SMX (88.5–91.9%) from actual surface water demonstrated that the matrix effect on the process performance was minimal in realistic applications, highlighting this novel REM to be a viable way to remove trace organic contaminants from surface water.
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RSC Advances
·
2019
·Vol. 9
·期 29
·16288-16295
·
IF 3.049
Shu-ying Zhen,Hai-tao Wu,Yan Wang,Na Li,Hao-sen Chen,Wei-li Song,Zhen-hua Wang,Wang Sun,Ke-ning Sun
Herein, hollow porous CuO–CuCo2O4 dodecahedrons are synthesized by using a simple self-sacrificial metal–organic framework (MOF) template, which resulted in dodecahedron morphology with hierarchically porous architecture. When evaluated as a cathodic electrocatalyst in lithium–oxygen batteries, the CuO–CuCo2O4 composite exhibits a significantly enhanced electrochemical performance, delivering an initial capacity of 6844 mA h g−1 with a remarkably decreased discharge/charge overpotential to 1.15 V (vs. Li/Li+) at a current density of 100 mA g−1 and showing excellent cyclic stability up to 111 charge/discharge cycles under a cut-off capacity of 1000 mA h g−1 at 400 mA g−1. The outstanding electrochemical performance of CuO–CuCo2O4 composite can be owing to the intrinsic catalytic activity, unique porous structure and the presence of substantial electrocatalytic sites. The ex situ XRD and SEM are also carried out to reveal the charge/discharge behavior and demonstrate the excellent reversibility of the CuO–CuCo2O4 based electrode.
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Journal of Materials Chemistry A
·
2019
·Vol. 8
·期 1
·259-267
·
IF 10.733
Congcong Dang,Yu Wang,Biao He,Weibin Zhang,Feng Dang,Hongchao Wang,Yong Du
Searching for highly efficient and low cost electrocatalysts is an urgent challenge to provide high capacity and long cycle life Li–O2 batteries (LOBs). In this work, the highly efficient electrocatalytic properties of MoSi2 were first demonstrated using particles prepared by a solid–state reaction method. The surface was activated, playing a dominant role in the electrocatalytic performance. After acid etching to remove SiO2 impurities arising from the surface oxidation, MoSi2 exhibited excellent bifunctional electrocatalytic properties for LOBs. Mo6+ on the surface contributed to the initial low overpotentials of 0.45 V (3.2 V for the OER and 2.75 V for the ORR) and transformed into Mo4+ for a long cycle life. As a consequence, outstanding rate capabilities of 12 708 mA h g−1 at 100 mA g−1 and 10 794 mA h g−1 at 800 mA g−1, and excellent cycle durability of 215 and 90 cycles at a limited capacity of 1000 mA h g−1 at 200 and 500 mA g−1, respectively, were obtained for the MoSi2 cathode.
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