Journal of Materials Chemistry B
·
2021
·Vol. 9
·期 15
·3401-3411
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IF 6.331
Ming Wang,Miao Li,Yunli Wang,Yiran Shao,Yingchun Zhu,Shiping Yang
Hydroxyapatite (HA) has attracted wide attention for medical application due to its biocompatibility and bioactivity. However, the infection problems of HA remain among the leading reasons for implantation failure. Thus, it is urgent to endow HA biomaterials with antibacterial activity. Herein, the high antibacterial activity was achieved by introducing trace Mn3+ and H vacancy couples in HA through a facile heat-treatment strategy in air. The theoretical results indicated that Mn3+ was preferentially substituted for the Ca(2) site in the HA structure with a charge-compensating H vacancy appearing at the adjacent OH− site. The antibacterial tests showed that Mn-HA possessed antibacterial activity towards both E. coli and S. aureus with trace Mn content at the ppm level, and implied that Mn3+ and centers may play an important role in the antibacterial process. The Mn3+ and couples in Mn-HA, serving as oxidative and reductive centers respectively, could then collectively participate in the CoQ/CoQH2 redox cycling and synergistically facilitate the accumulation of CoQ˙− and ROS radicals. This enhanced ROS production was the main factor to endow Mn-HA with efficient antibacterial activity. Moreover, the in vitro bioactivity assay showed that Mn-HA materials exhibited enhanced osteogenic activity and good biocompatibility. Therefore, this work not only provides a feasible method to control the oxidation state of Mn elements in HA, but also proposes a novel trace Mn3+-doped HA for potential applications in tissue engineering.
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LIQUID CRYSTALS
·
2014
·
IF 2.349
Fafu Yang,Jin Yuan,Congcong Li,Hongyu Guo,Xiaoyun Yan
Series of triphenylene derivatives with multiple NH groups 3a, 3b, 4a, 4b, 5a and 5b were designed and synthesised by simple procedures in high yields. Their structures were confirmed by Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR), mass spectrometry (MS) and elemental analysis. Their mesophase behaviours were studied by differential scanning calorimetry, polarising optical microscopy and X-ray diffraction. The triphenylene derivatives 3a and 3b with two NH groups and triphenylene derivatives 4a and 4b with three NH groups possess excellent mesomorphic properties. Compounds 4a and 4b exhibited wider mesophase than compounds 3a and 3b. Triphenylene derivatives 5a and 5b with five NH groups have no mesomorphic properties. These results suggested the units of hydrogen bonds played the crucial roles on mesomorphic properties and acylthiosemicarbazide group with three NH groups was a good functional group for producing excellent mesomorphic properties.
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Evidence-based Complementary and Alternative Medicine
·
2013
·
IF 1.722
Huiqing Lv,Xiaoping Zhang,XueZhi Chen,Zhijun Xie,Changfeng Hu,Chengping Wen,Kezhi Jiang
Background. Ficus pandurata H. (Moraceae) is widely used in traditional Chinese medicine as a healthy food condiment or a medicine for treatment of various diseases including inflammation. Objective. The purpose of the present study is to investigate the phytochemical compositions and antioxidant and anti-inflammatory activities of crude water (FPW) and ethanolic extracts (FPE) from Ficus pandurata H. Methods. Phytochemical compositions were identified by a high-performance liquid chromatography-electrospray ionization-mass spectrometry method (HPLC-ESI-MS). The antioxidant activities were evaluated by diphenylpicrylhydrazyl (DPPH) and hydroxyl radical assays, and the anti-inflammatory activities were evaluated by paw edema and levels of inflammatory mediator TNF-α and PGE2 in monosodium urate (MSU) crystal-induced rats. Results. Six compounds were identified by HPLC-MS method, and abundance of phenolics was found in FPE. The FPE showed concentration-dependent-significant scavenging of DPPH and hydroxyl radicals with IC50 values 118.4 and 192.9 μg/mL, respectively. The FPE treatment significantly inhibited the paw edema and the production of TNF-α and PGE2 in MSU crystal-induced rats. Conclusion. The FPE exerted stronger antioxidant and anti-inflammatory activities which may be attributed to its high phenolic content.
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PROGRESS IN ORGANIC COATINGS
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2017
·
IF 2.858
Fei Gao,Jiancheng Cao,Qibo Wang,Ren Liu,Shengwen Zhang,Jingcheng Liu,Xiaoya Liu
A series of ultraviolet (UV)-curable self-healing polyurethane (PU) oligomers were synthesized by incorporating different contents of 2-ureido-4[1H]-pyrimidone and polycarbonate diols (PCDL) with different molecular weights at the end of PU chains. The structure of the oligomers were determined through Nuclear magnetic resonance ( 1 H NMR) and Fourier transform infrared spectroscopy. The PU oligomers were used to produce UV-curable self-healing coatings, the properties of which were investigated and the properties of the coatings with different functionality were studied. The results revealed that the performance of the coating was higher when a higher molecular weight of PCDL was used and With functionality increasing, the crosslinking density of the coating ascends, resulting in higher self-healing temperature and upper pendulum hardness and gloss of the coating. To balance the self-healing ability and mechanical properties of the coating, a series of coating formulations were designed by adding different types and amounts of active diluents. Double bond conversion, thermostability, and self-healing ability were investigated to determine the effect of active diluents on coating performance. The results demonstrated that the resultant coating have excellent adhesion, gloss, and thermostability. Coatings prepared used all types of active diluents had favorable self-healing ability, except for that prepared using 2-acryloyloxymethyl-2-ethyltrimethylene diacrylate. Excellent self-healing and mechanical properties were obtained when 20 w.t.% of triethoxylated trimethylolpropane triacrylate was used.
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JOURNAL OF PHYSICS D-APPLIED PHYSICS
·
2025
·Vol. 58
·期 20
·205501
·
IF 3.2
Fan Li,Chuansheng Zhang,Yi Luo,Xiaoxiao Kong,Cheng Zhang,Boxue Du,Tao Shao
Hexagonal boron nitride (h-BN) has emerged as a critical thermal management material in electrical insulation systems due to its superior thermal conductivity and dielectric properties. Nevertheless, suboptimal filler-matrix interfacial compatibility hinders both thermal conductivity enhancement and dielectric performance in composites. This study introduces an innovative plasma bubble treatment strategy, utilizing the discharge within bubbles to simultaneously achieve h-BN exfoliation and surface hydroxylation. By producing plasma in a 3% H2O2 solution with Ar/O2 mixed gas, hydroxyl groups are successfully grafted onto h-BN surfaces. This surface modification improves the silane grafting efficiency with KH560, resulting in improved filler dispersion within the epoxy resin (EP) and the introduction of deep charge traps in interfacial regions. Under 9.77 W discharge power, composites containing 20 wt% h-BN treated for 10 min exhibits optimal performance characteristics. The modified composite attains a 327% thermal conductivity of pure EP while showing superior dielectric properties with a 12.4% increase in breakdown strength relative to untreated composite. These findings present an effective surface engineering approach for developing high-performance polymer composites for electrical insulation applications.
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CERAMICS INTERNATIONAL
·
2025
·
IF 5.6
Jie Zhou,Siyuan Jin,Ruizhi Wu,Xiaochun Ma,Mengyao Pang,Zhe Yu,Guixiang Wang,Jinghuai Zhang,Boris Krit,Sergey Betsofen,Vitalii Neshchimenko,Buzikov Ruslan,Min Qiu,Yurong Yang,Jiaming Chen
Microarc oxidation (MAO) coatings incorporating hexagonal boron nitride (h-BN) nanoparticles were synthesized on Mg-Li alloys. The effects of h-BN nanoparticle concentration on the structure, phase composition, and tribological properties of the MAO coatings were systematically investigated. The results indicate that the addition of h-BN nanoparticles induces the formation of protrusions on the coating surface, varied in size and distribution with the concentration of h-BN particles. The protrusions are advantageous for enhancing the wear resistance of the coating, owing to the effective reduction of the contact area and the lubricating impact of the released h-BN particles during wear. The thickness and hardness of the coating contained h-BN particles are significantly elevated. At an optimal h-BN concentration of 7 g/L, the composite coating exhibits the lowest average coefficient of friction (COF = 0.59) and the minimum wear rate (W = 2.6 × 10 −6 mm 3 /N·m), thereby demonstrating superior tribological performance.
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Journal of Energy Chemistry
·
2023
·
IF 13.1
Yuzhu Qian,Hongrui Wang,Xinni Li,Ting Song,Yong Pei,Li Liu,Bei Long,Xiongwei Wu,Xianyou Wang
The development of insertion-type anodes is the key to designing “rocking chair” zinc-ion batteries. However, there is rare report on high mass loading anode with high performances. Here, {001}-oriented BiOCl nanosheets with Sn doping are proposed as a promising insertion-type anode. The designs of cross-linked CNTs conductive network, {001}-oriented nanosheet , and Sn doping significantly enhance ion/electron transport, proved via experimental tests and theoretical calculations (density of states and diffusion barrier). The H + /Zn 2+ synergistic co-insertion mechanism is proved via ex situ XRD, Raman, XPS, and SEM tests. Accordingly, this optimized electrode delivers a high reversible capacity of 194 mA h g −1 at 0.1 A g −1 with a voltage of ≈0.37 V and an impressive cyclability with 128 mA h g −1 over 2500 cycles at 1 A g −1 . It also shows satisfactory performances at an ultrahigh mass loading of 10 mg cm −2 . Moreover, the Sn-BiOCl//MnO 2 full cell displays a reversible capacity of 85 mA h g −1 at 0.2 A g −1 during cyclic test.
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JOURNAL OF THE EUROPEAN CERAMIC SOCIETY
·
2023
·
IF 5.7
Yage Li,Shuaibing Wu,Feng Liang,Gongye Lv,Yu Tian,Haijun Zhang,Yong Liu,Guoqi Liu
Rod-like h-BN with an average diameter of 2 µm was synthesized at a relatively low temperature of 1200 °C through a catalytic pyrolysis precursor strategy using boric acid and melamine as starting materials, and Co(SO 3 NH 2 ) 2 ·4 H 2 O as a catalyst precursor. Subsequently, novel low-carbon Al 2 O 3 -C refractories were prepared via a replacement of the graphite with the as-synthesized rod-like h-BN. When 1 wt% h-BN rods were added to replace graphite, after 3 h coking at 1400 °C, the cold modulus of rupture, cold compressive strength , oxidation resistance , and thermal shock resistance of the specimen were increased by 16.4%, 24.8%, 31.2%, and 52.2%, respectively, compared with these of the control specimen. Moreover, the introduction of h-BN rods in the matrix enhanced the non-wetting ability of the refractory with molten slag, thus the rod-like h-BN modified low carbon refractory presented better slag corrosion resistance with reference to the specimen without h-BN rods.
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PROGRESS IN ORGANIC COATINGS
·
2020
·
IF 4.469
Hongyi Shi,Weiqu Liu,Chunhua Liu,Maiping Yang,Yankun Xie,Shuo Wang,Fengyuan Zhang,Liyan Liang,Ke Pi
Herein, h-BN powders were sonicated in an aqueous solution of polyethylenimine (PEI) to simultaneously exfoliate and functionalize h-BN nanosheets with Lewis acid-base interaction. The structure and morphology of PEI modified h-BN nanosheets (PEI-BNNSs) were characterized by FTIR, TGA, AFM and TEM. The as-prepared PEI-BNNSs were served as anticorrosive nanofillers for waterborne epoxy (EP) coatings on Q235 carbon steel. The corrosion behaviors of EP and PEI-BNNSs/EP coating systems in 3.5 wt % NaCl aqueous solution were evaluated by electrochemical workstation. It is worth noting that the protection efficiency (PE) values of 1 wt % PEI-BNNSs/EP and 2 wt % PEI-BNNSs/EP coating systems are as high as 99.99 % compared to EP coating systems. Moreover, the impedance modulus (|Z| f = 0.01 Hz ) of the 1 wt % PEI-BNNSs/EP coating system was 3–4 orders of magnitude higher than the EP coating after 90 days of immersion. The electrochemical results revealed that PEI-BNNSs can significantly enhanced the corrosion resistance of waterborne epoxy coatings.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2022
·
IF 7.139
Qu Tang,Xiaobo Zhou,JinXia Liu,Mingmin Wu,Haiwei Ji,Qi Wang,Guo Li,Hui Cong,Yuling Qin
The use of Formic acid as an alternative to fossil fuels is promising, both from economical and ecological standpoints, and has received great of attention owing to its inherently superiority in recent decades. Nevertheless, efficient and low-cost solid catalyst for formic acid dehydrogenation at room temperature still constitutes a biggish challenge. Moreover, comparing to increase the catalytic performance of catalysts, very little attention payed to the kinetic mechanism of dehydrogenation reaction because of the lack of effective characterization artifice. Here, the as-prepared Ni@Pd nanoparticles by a sequential reduction process can be useful catalyst for formic acid decomposition at room temperature without a promoter. Thanks to the effective catalyst and isotope distribution technique, preliminary mechanistic results firstly reveal that hydrogen is obtained via a H-atom recombination on isolated sites after the proton exchange randomly between activated H and solvent.
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RESOURCES CONSERVATION AND RECYCLING
·
2021
·
IF 10.204
Liming Yang,Genping Yi,Bo Wang,Penghui Shao,Yufa Feng,Yanbiao Liu,Kai Yu,Fuqiang Liu,Lingling Liu,Xubiao Luo,Shenglian Luo
Simultaneous recovery and value-added conversion of hazardous heavy metal ions from complex wastewater sources is of great significance yet challenging. Herein, we demonstrate that highly toxic antimonite Sb(III) could be effectively recovered from antimony (Sb) mine flotation wastewater and converted into high-value-added metallic Sb using a novel facile atomic H* enhanced electrochemical reduction avenue coupled with thermal reduction by H 2 gas. The high production of atomic H* generated from the electrochemical cathode with an optimum reduction potential of –1.2 V vs . Ag/AgCl, which is lower than the Sb(III) reduction potential of –1.0 V, might be attributable to the superior Sb recovery capabilities. Furthermore, the metallic Sb concentration at –1.2 V was 14.43 times greater than at –1.0 V due to the strong reductivity of atomic H*. In addition, Sb(III) removal efficiency was found to be as high as 98.52%, with a metallic Sb recovery rate of up to 1.67 mg min –1 . The efficiency of Sb(III) recovery was demonstrated throughout a wide pH range, with metallic Sb being the main product, independent of the presence of multiple coexisting ions. Economic analysis also indicated that treating Sb mine flotation wastewater per ton may yield a net profit of $40.09. This research contributes to the advancement of an atomic H* enhanced electrochemical technology for high-valued heavy metal recovery from complex heavy metal-polluted wastewater.
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DALTON TRANSACTIONS
·
2020
·Vol. 50
·期 3
·1060-1068
·
IF 4.174
Run-Ze Yuan,Peng-Fei Cui,Shu-Ting Guo,Guo-Xin Jin
Herein, we describe the synthesis of tetraphenylphosphonium o-carboranyl dithiocarboxylate (Ligand 1) and methyldithiocarboxyl-o-carborane (Ligand 2). The complexes [Cp*M(o-C2B10H11CS2)Cl] (M = Ir (3); Rh (4)) and [Cp*M(o-C2B10H11CS2)2] (M = Ir (5); Rh (6)) have been synthesized based on Ligand 1. The selective B–H bond activation of Ligand 2 has also been explored, leading to the synthesis of the B–H activated complex [Cp*Ir(o-C2B10H10CS2CH3)Cl] (7) and four of its substituted derivatives (8, 9, 10 and 11). All of these compounds have been characterised through single-crystal X-ray diffraction, NMR, IR spectroscopy and elemental analysis.
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