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Scientific Reports · 2021 ·Vol. 11 ·期 1 ·1-9 · IF 4.38

Co-administration of lipopolysaccharide and d-galactosamine induces genotoxicity in mouse liver

Dong Wenjing,Song Erqun,Song Yang

The acute liver injury (ALI) and hepatic fibrosis caused by the co-treatment of lipopolysaccharide (LPS)/ d -galactosamine (D-GalN) have been extensively studied. However, whether LPS/D-GalN are genotoxic has been left unknown. In this study, male mice were divided into eight groups with eight animals in each group. For acute challenge of LPS/D-GalN, the mice in each group received a combination of LPS/D-GalN via intraperitoneal injection at the dose of 25 μg/kg/250 mg/kg, 25 μg/kg/500 mg/kg, or 50 μg/kg/500 mg/kg body weight. An additional group for chronic administration of test compounds was conducted by i.p. injection of LPS/D-GalN (10 μg/kg/100 mg/kg) every other day for 8 weeks. Saline solution (0.9%) and cyclophosphamide (CTX) (50 mg/kg body weight) given by i.p. injection was used as the negative and positive control, respectively. The results of single cell gel electrophoresis (SCGE) assay indicated that acute exposure of the mice to LPS/D-GalN caused severe DNA damage in hepatic cells, but not in the brain, sperm or bone marrow cells, which evidenced the genotoxicity of LPS/D-GalN administrated in combination. Interestingly, the chronic administration of LPS/D-GalN triggered significant genotoxic effects not only in hepatic but also in brain cells, with negative results in sperm and bone marrow cells. Histopathological examination in the liver and brain tissues revealed changes consistent with the SCGE results. The present study indicates genotoxic potential of LPS/D-GalN co-administered in mice, which may serve as an in vivo experimental model for relevant genotoxic study.

CAS / MDL: 1772-03-8 93572-42-0
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JOURNAL OF THE AMERICAN CERAMIC SOCIETY · 2020 ·Vol. 103 ·期 12 ·6847-6859 · IF 3.502

Visible emission and energy transfer in Tb3+/Dy3+ co-doped phosphate glasses

Yan Sun,Fei Yu,Meisong Liao,Juping Ma,Xin Wang,Dongbing He,Weiqing Gao,Jonathan Knight,Lili Hu

In this work, we systematically study the spectroscopic properties of Tb 3+ /Dy 3+ co-doped phosphate glasses in the visible spectral region and explore the sensitization role of Dy 3+ in the enhancement of visible fluorescence of Tb 3+ ions. Judd-Ofelt parameters Ω 2 and Ω 4 /Ω 6 of the phosphate glass as host for Tb 3+ are calculated as 21.60 × 10 -20 cm 2 and 0.73, respectively, based on the measured spectral absorption. Multiple energy transfer (ET) routes from Dy 3+ to Tb 3+ and their efficiencies are characterized, and the enhanced fluorescence properties of Tb 3+ are investigated, including the emission spectral strength and the spontaneous emission lifetime as functions of Dy 3+ doping concentration. The efficient nonradiative ET processes between Dy 3+ and Tb 3+ allow a moderate concentration level of Tb 3+ to achieve favorably stronger spectral absorption at blue and ultraviolet wavelengths. Tb 3+ /Dy 3+ co-doped phosphate glass shows promising potential for phosphors and lasing operation at visible wavelengths.

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CERAMICS INTERNATIONAL · 2020 · IF 3.83

In situ synthesis hydrophobic Co/CoO/C nanofibers with enhanced microwave absorption

Yuchen Zhang,Yongqian Shen,Minmin Dang,Fan Zhang,Xueyan Du

Carbon nanofiber composites could be used as a microwave absorbing candidate owing to its lightweight and dielectric properties . In this work, the carbon-based nanofibers were synthesized using cobalt acetate tetrahydrate (CoAc)/poly (vinyl alcohol) (PVA) as a precursor solution via the electrospinning and vacuum carbonization at 650 °C. Co and CoO were simultaneously introduced into carbon nanofibers (CNFs). The CNFs absorber with an especially low filling ratio of 10% exhibited excellent microwave absorbing properties. The minimum reflection loss (RL) reached −43.57 dB at 10.48 GHz with a matching thickness of 3 mm, and the wideband effective absorption (RL ≤ −10 dB) reached 5.78 GHz (10.94–16.72 GHz) at 2.5 mm. The superior absorption performance of the as-prepared CNFs resulted from the formation of CoO, causing the improvement of impedance matching and interfacial polarization. Besides, the CNFs displayed good hydrophobicity due to the roughened surfaces. These newly synthesized Co/CoO/CNFs might be considered as a prospective candidate for highly efficient microwave absorption materials with a self-cleaning function.

CAS / MDL: 9002-89-5
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2020 · IF 4.939

Co/VN heterostructure coated with holey interconnected carbon frameworks as bifunctional catalysts

Tianlun Cen,Lijun Qiu,Zhifeng Ye,Xiaomin Peng,Yiyi Liu,Dingsheng Yuan

The development of transition-metal electrocatalyst is of great importance to bring down costs and enhance performance for fuel cells and water splitting. The multiple efforts have been concentrated on bifunctional electrocatalysts toward hydrogen evolution reaction (HER) and oxygen reduction reaction (ORR). Only a few works reach desirable durability and performance levels. Here, Co/VN heterostructure with rational porous structure is formed in response to the sensible cobalt and vanadium ratio. Owing to synergistic interaction of holey interconnected structure with large surface area of 57 m 2  g −1 and abundant interfaces between Co and VN phases, Co/VN@NC presents superior bifunctional electrocatalytic performance towards both HER and ORR. Co/VN@NC drives the reaction with low overpotential η 10 of 96 mV and Tafel slope of 82 mV dec −1 along with outstanding stability for HER. Furthermore, Co/VN@NC obtains an onset potential (0.954 V) and half-wave potential (0.796 V) with superior methanol tolerance and durability for ORR.

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SURFACE ENGINEERING · 2020 · IF 2.433

Preparation of Co–P–TiO2 nanocomposite coatings via a pulsed electrodeposition process

Zhen He,Di Cao,Yuxin Wang,Li Yin,Muhammad D. Hayat,Harshpreet Singh

A series of Co–P–TiO2 nanocomposite coatings were prepared via pulsed electrodeposition technique. TiO2 nanoparticles were embedded into the coating matrix using TiO2 sol. The phase constituents of nanocomposites were identified using X-ray diffraction. The surface morphology of nanocomposites was obtained through scanning electron microscopy. Wear tests and corrosion tests were conducted to determine the coating performance. Electrochemical characterization was performed by electrochemical impedance spectroscopy analysis. The nanocomposite coatings made via conventional pulse electrodeposition had a relatively ordered surface morphology and enhanced mechanical behaviour, which is associated with the increased strengthening effect of embedded nanoparticles. When applying a pulse reverse current, the Co–P–TiO2 nanocomposite coating had improved corrosion resistance owing to its smooth and uniform surface morphology.

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JOURNAL OF MATERIALS SCIENCE · 2020 ·Vol. 55 ·期 24 ·10878-10895 · IF 3.553

Tough, high-strength PDAAM-co-PAAM hydrogels synthesized without a crosslinking agent

Qiao Liyuan,Liu Cheng,Liu Chengde,Cheng Xitong,Li Yizheng,Wang Chenghao,Jian Xigao

Hydrogels find a variety of uses across various fields, but their development might be limited by their high-cost, toxic chemical crosslinking and complicated reactions. To address these issues, we developed a tough, high-strength hydrogel of polydiacetone acrylamide-co-poly(acrylamide), prepared using acrylamide, diacetone acrylamide (DAAM) and ammonium persulfate in a one-step reaction. The multiple physical crosslinking networks endow hydrogel with excellent overall properties given appropriate DAAM levels. The tensile modulus, fractured strain, fractured stress and toughness of the developed D 1 A 9 hydrogel are, respectively, as high as 0.15 MPa, 21 mm/mm, 0.71 MPa and 7 MJ/m 2 . Its compressive modulus under a strain of 80% is 0.088 MPa, while its shear modulus at a shear frequency of 100 Hz is 0.071 MPa. At the same time, D 1 A 9 hydrogel exhibits a high self-recovery efficiency of 50% during two continuous cyclic tensile tests, with the efficiency increasing to 65% for hydrogel incubated at 50 °C for 2 h. Finally, cytocompatibility and excellent drug-releasing behavior of the hydrogel make it a candidate for biomedical use.

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JOURNAL OF MATERIALS SCIENCE · 2020 ·Vol. 55 ·期 27 ·13216-13231 · IF 3.553

Electrospun Mg/poly(lactic-co-glycolic acid) composite scaffold for urethral reconstruction

Huang Liqu,Wang Xianli,Zhang Yue,Cheng Zhaojun,Xue Feng,Guo Yunfei,Deng Yongji,Chu Chenglin,Tao Li,Bai Jing

Hypospadias is a common congenital malformation of the male urogenital system. As a recently arisen reconstruction method for hypospadias, polymer tissue engineering urethral scaffold often results in necrosis and other complications due to the lack of bioactivity. To improve the bioactivity of polymer, in this work, we prepared biodegradable Mg/poly(lactic-co-glycolic acid) (PLGA) composite nanofiber scaffolds by electrospun with 3, 6, and 9 wt.% of micron-scale Mg particles. The mechanical properties of the PLGA scaffold gradually decrease with the addition of Mg particles but still at an acceptable level. On the other hand, these composite scaffolds show very good biocompatibility and promotional bioactivity, namely non-cytotoxicity, gradual proliferation enhancement, and good adhesion state of human adipose stem cells (HADSCs) on the scaffold surface. Besides, through quantitative real-time polymerase chain reaction (qRT-PCR) test, different genes expression levels of human umbilical vein endothelial cells (HUVECs) were also gradually up-regulated with the increase in Mg content. The present results indicate that Mg containing PLGA scaffolds might not only have the potential to promote tissue regeneration related to urethral repair, but also stimulate endothelial cells to achieve vascularization and anti-inflammatory functions. Consequently, considering both the mechanical properties and bioactivity for clinical demand, the Mg/PLGA composite scaffolds with suitable Mg contents are promising for the regeneration of defective urethral tissues.

CAS / MDL: 920-66-1
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2020 ·Vol. 27 ·期 21 ·26810-26816 · IF 3.056

Defected graphene as effective co-catalyst of CdS for enhanced photocatalytic activities

Chen Ying,Wang Yue,Zhou Xiaohan,Zhao Yang,Peng Wenchao

Synthesis of highly efficient photocatalysts for energy and environment catalysis is still a big challenge in the materials field. Cadmium sulfide (CdS) is a promising visible light-driven photocatalyst, which can be composited with co-catalysts to increase its photo-activity and stability. In this study, a kind of graphene material with abundant structure defects (D-rGO) is synthesized by a two-step annealing process with nitrogen-doped rGO (N-rGO) as an intermediate. The high-temperature annealing could remove the doped heteroatoms to form structure defects with five or seven carbon atoms. The D-rGO is then used as co-catalyst for the modification of CdS nanoparticles, and enhanced photocatalytic activities could be obtained. A large hydrogen evolution rate of 102.7 μmol h −1 g −1 is achieved, which is also effective for 4-nitrophenol reduction with a rate constant of 0.168 min −1 . The novel CdS/D-rGO composite contains no noble metals and could be used as multi-functional photocatalysts, thus should has great potential in the photocatalysis field.

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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2020 · IF 5.162

Kinetics of partially depolymerized lignin as co-curing agent for epoxy resin

Zhengyi Zhang,Jiaoman Li,Yan Zhang,Zhenfu Jin

Lignin, which is crosslinked by ether and carbon‑carbon linkages, is a highly branched polymer consisting of phenyl propane units. And owing to the abundant phenolic hydroxyl groups and its structural heterogeneous characteristics, lignosulfonate, considered as a renewable aromatic macropolymer, can be used as co-curing agent in EP thermoset systems. In this study, kinetics of lignosulfonate (LS) and partially depolymerized lignosulfonate (DLS) as co-curing agents for applications to EP thermoset were discussed with the differential scanning calorimetry (DSC) measurement. The activation energy ( E a ) and dynamic modeling of curing reaction were obtained by the methods of non-isothermal kinetic analysis reported by Kissinger and Ozawa. The glass transition temperature ( T g ) was determined by DSC and mechanical properties of epoxy resins were carried out using the Universal Testing Machine. The LS dropped the exothermic peak temperature and E a of curing reaction of EP thermoset. Those of DLS were more active than the higher molecular weight lignosulfonate. The EP thermoset cured with DLS (EP-DLS) exhibited much higher reactivity, and the curing reaction could be occurred at lower temperature. The T g of EP-DLS has risen by 10 °C compared with the case without lignosulfonate. The tensile strength , elongation at break and impact strength of EP-DLS rose by 28.7%, 52.5% and 53.5%, respectively, than those of the epoxy resin cured with LS (EP-LS).Molecular weight of lignosulfonate could be an important factor of the curing reaction of EP thermoset. The high performance EP thermoset could be obtained by partially depolymerized lignin as co-curing agents.

CAS / MDL: 103-83-3
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2020 · IF 16.683

Dual-atom Ag2/graphene catalyst for efficient electroreduction of CO2 to CO

Yifan Li,Chang Chen,Rui Cao,Ziwei Pan,Hua He,Kebin Zhou

Electrochemical reduction of CO 2 into value-added carbon compounds offers a promising strategy to mitigate global warming, but present challenges for chemistry due to the poor selectivity and stability of electrocatalysts. In this work, we report a dual-atom Ag 2 /graphene catalyst featuring well-defined AgN 3 -AgN 3 active site for CO 2 electrochemical reduction. This dual-atom catalyst can drive CO 2 reduction reaction at a potential as high as -0.25 V, and exhibit excellent CO Faradic efficiency up to 93.4 % with a current density of 11.87 mA cm −2 at -0.7 V and long-term stability, far surpassing the single-atom Ag 1 /graphene and the traditional silver nanoparticle catalysts. DFT calculations reveal that the dual-atom Ag site lowers the barrier for the formation of *COOH by stabilizing the *CO 2 through the concomitant interactions with the C and an O atom of CO 2 , resulting in excellent catalytic performance.

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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2021 · IF 8.128

One-dimensional Ni@Co/C@PPy composites for superior electromagnetic wave absorption

Yuxin Bi,Mingliang Ma,Zijian Liao,Zhouyu Tong,Yan Chen,Rongzhen Wang,Yong Ma,Guanglei Wu

The conductive networks for electron hopping and migration constructed by one-dimensional (1D) composite absorbers are highly desirable to improve the electromagnetic (EM) wave attenuation capacity. Herein, the Ni@Co/C@polypyrrole (PPy) composites integrating the advantages of component and microstructure were fabricated. The addition of Co/C and PPy effectively optimized the impedance matching and improved the EM attenuation. Under the comprehensive impacts of multiple reflections/scattering, conduction loss and interface polarization, the Ni@Co/C@PPy composites showed superior EM wave absorption with the reflection loss (RL) value of −48.76 dB and the effective absorption bandwidth (EAB) of 5.10 GHz at a corresponding thickness of 2.0 mm. The largest EAB could reach 5.54 GHz (7.24–12.78 GHz) at the thickness of 2.2 mm. This work provides a great reference for fabricating 1D novel EM wave absorption materials.

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APPLIED SURFACE SCIENCE · 2021 · IF 6.707

Dual heteroatoms co-doping strategy of graphene-based dielectric loss electromagnetic absorbent

Zhihao Sun,Zhaoqian Yan,Anran Li,Kaicheng Yue,Lanling Zhao,Lei Qian

In this paper, the modulation of microwave absorption performance through diatomic co-doping was systematically investigated. N, S co-doped reduced graphene oxide (NS-rGO) and S, B co-doped rGO (SB-rGO) were obtained by one-pot hydrothermal reaction and freeze-drying. The experimental results and theoretical calculations suggested that the charge distribution of N, B and S heteroatoms with adjacent C atoms obviously changed, which effectively regulated the electronic transmission and polarization state, and accordingly affected the dielectric response. Besides, compared to N-rGO and B-rGO, impedance matching characteristics and electromagnetic attenuating capability of NS-rGO and SB-rGO were significantly enhanced due to the synergistic regulation of pyrrolic N, pyridinic N, -CBO 2 -, B-C 3 and -C-SO 2 -C- bonds. NS-rGO exhibited the minimum reflection loss (RL min ) of −52 dB at 10 GHz under an ultra-low loading of 2 wt%, and its effective absorption bandwidth (EAB, below −10 dB) ranged from 7 GHz to 18 GHz in the thickness of 2.0–3.8 mm. SB-rGO also exhibited the RL min of −54.2 dB at 11.8 GHz under an ultra-low loading of only 1.5 wt%, and the EAB of 12 GHz (6–18 GHz) in the thickness of 2.0–3.8 mm. This work offers a deep insight into the relationship among dual atoms co-doping, dielectric performance and microwave absorption property.

CAS / MDL: 1313-84-4
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