ACS Applied Materials & Interfaces
·
2025
·
IF 8.2
Shuai Wang,Yuqi Chen,Shuyan Zheng,Yanan Yuan,Kexin Du,Min Cui,Yue Wu,Ping Li,Wei Hu,Jingui Wang,Yingshu Guo,Zexing Wu,Yanli Zhao
The incorporation of sp-hybridized nitrogen arisen from graphdiyne (GDY) into the catalyst structure significantly improves the electrocatalytic efficiency of zinc–air batteries by modulating the electronic properties of the active sites, thereby accelerating reaction kinetics and enhancing conductivity. This work highlights the efficacy of the Co–N-GDY catalyst, where sp-N moieties in GDY serving as anchoring centers for cobalt species, which demonstrates exceptional performance in the oxygen reduction reaction, achieving a half-wave potential of 0.85 V, along with high oxygen evolution reaction performance that surpasses that of commercial Pt/C + IrO2-based batteries. The Co–N-GDY catalyst also exhibits commendable cycling stability with minimal fluctuation in voltage difference, indicating its suitability for practical applications in advanced energy storage systems. These findings underscore the importance of developing cost-effective and durable M–N–C catalysts to enhance the commercial viability and sustainability of zinc–air battery technology.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2022
·Vol. 47
·期 47
·20561-20571
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IF 7.139
Tianyu Ai,Jing Li,Shuai Nie,Yansheng Yin,Jinlin Lu,Shuo Bao,Ling Yan
Transition elements doping metal oxide is of great significance for developing gas sensors with high performance. To achieve this goal, α-Fe 2 O 3 rod and Mn-doped α-Fe 2 O 3 polyhedrons are successfully synthesized by a facile N, N-dimethylformamide assisted hydrothermal method and characterized by several physical techniques. The morphology of α-Fe 2 O 3 is evolved by introducing Mn elements. The performance of the α-Fe 2 O 3 rod and Mn-doped α-Fe 2 O 3 polyhedrons as H 2 gas sensors are studied and compared. The Mn/α-Fe 2 O 3 -5 polyhedrons sensor exhibit the best performance at optimum operating temperature of 300 °C. The response and recovery times are 10 s/24 s for H 2 with a concentration of 200 ppm, which is much faster in contrast to those recently reported H 2 gas sensors. Furthermore, α-Fe 2 O 3 rod and Mn-doped α-Fe 2 O 3 polyhedrons show abnormal n-p transition sensing behavior with the change of operating temperature. This work provides a facile method for synthesizing α-Fe 2 O 3 based sensing materials for various sensors applications.
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RSC Advances
·
2015
·Vol. 5
·期 26
·19859-19864
·
IF 3.84
Junjun Li,Lin Zhang,Jin Gu,Yuping Sun,Xiaosheng Ji
To retain the hydroxyl group of poly(vinyl alcohol) (PVA), ammonium persulfate (APS) was used to initiate the polymerization of hydrogen on the PVA chain. Rather than hydroxyl-based cross-linking, the generated PVA macromolecule radicals were cross-linked with N,N′-methylene bisacrylamide (MBA) to prepare PVA membranes. The PVA membranes were shown to be successfully cross-linked via FT-IR characterization, as well as measurements of swelling degree and gel fraction. With increasing the content of cross-linker, the swelling degree of the membranes decreased, and the gel fraction increased. The pervaporation performance of the membrane was investigated by separating 95 wt% ethanol aqueous solutions. The cross-linked PVA membrane containing 0.5 wt% cross-linker yielded a high permeate water content (99 wt%) and a total flux of 353 g m−2 h−1 at 40 °C. As the feed temperature increased, the total flux increased, while the permeate water content decreased. The cross-linked membrane exhibited good durability over long-term operation.
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POLYMER
·
2025
·
IF 4.5
Huiling Huang,Shengqi Cui,Xiaoqing Song,Zhonglin Luo,Biaobing Wang
It is still a great challenge to achieve flame retardant epoxy resin (EP) without sacrificing its transparency and mechanical properties. In the present work, A P/N/S containing sulfonamide compound (DPPBSA) was synthesized and adopted to improve the fire safety of transparent epoxy resin. With the incorporation of 5 wt% DPPBSA, the EP composite presented UL-94 V-0 rating and 35.4% of LOI value, its peak of heat release rate and total heat release were also reduced by 51.0% and 40.8% as compared with the pure EP, respectively. The improved flame retardancy was attributed to the comprehensive flame retardant effect of the P, N, and S elements. In the condensed phase, much continuous and denser char layers with greater graphitization degree were formed during the combustion. In the gas phase, the pyrolysis of the DPPBSA released dilution gases and P-containing free radical scavengers. Moreover, the EP composite containing 5 wt% DPPBSA displayed almost comparable tensile strength and transparency with the pure EP.
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RSC Advances
·
2026
·Vol. 16
·期 21
·19213-19224
·
IF 6.1
Jingdong Nong,Zhonghua Sun,Weiyou Zhou,Zhong Wu,Junfeng Qian,Qun Chen,Mingyang He
A series of Cu-modified Ni–Al2O3 catalysts with various Cu/Ni ratios (xCu/Ni–Al2O3) were prepared, and systematically characterized using BET, XRD, SEM, H2-TPR, H2-TPD, TG, and XPS. The catalyst exhibited excellent catalytic performance in the selective hydrogenation of N,N-dimethylaniline to N,N-dimethylcyclohexylamine in a continuous fixed-bed reactor. When the Cu/Ni molar ratio was 0.1, the active components were highly dispersed on the Al2O3 support, which possessed a high specific surface area and well-developed porous structure. Furthermore, the catalyst demonstrated strong hydrogen desorption capacity and enhanced thermal stability. Synergistic electronic interactions between Ni and Cu improved the adsorption and activation of both reactant and H2 molecules. The incorporation of Cu near the Ni active sites effectively modulated the selectivity toward the desired product N,N-dimethylcyclohexylamine. Under the optimal reaction conditions: H2 pressure of 5 MPa, reaction temperature of 130 °C, liquid hourly space velocity 0.1 h−1 and hydrogen-amine volume ratio of 5500 : 1, the 0.1Cu/Ni–Al2O3 catalyst achieved superior performance, with a N,N-dimethylaniline conversion rate of 99.5% and a selectivity for N,N-dimethylcyclohexylamine of 97.6%.
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INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
·
2023
·Vol. 24
·期 2
·1274
·
IF 5.6
Yuanhang Zhao,Hong Zhang,Lihua Hong,Xinying Zou,Jiazhuo Song,Rong Han,Jiawen Chen,Yiyan Yu,Xin Liu,Hong Zhao,Zhimin Zhang
Dental caries, particularly secondary caries, which is the main contributor to dental repair failure, has been the subject of extensive research due to its biofilm-mediated, sugar-driven, multifactorial, and dynamic characteristics. The clinical utility of restorations is improved by cleaning bacteria nearby and remineralizing marginal crevices. In this study, a novel multifunctional dental resin composite (DRC) composed of Sr-N-co-doped titanium dioxide (Sr-N-TiO2) nanoparticles and nano-hydroxyapatite (n-HA) reinforcing fillers with improved antibacterial and mineralization properties is proposed. The experimental results showed that the anatase-phase Sr-N-TiO2nanoparticles were synthesized successfully. After this, the curing depth (CD) of the DRC was measured from 4.36 ± 0.18 mm to 5.10 ± 0.19 mm, which met the clinical treatment needs. The maximum antibacterial rate againstStreptococcus mutans(S. mutans) was 98.96%, showing significant inhibition effects (p< 0.0001), which was experimentally verified to be derived from reactive oxygen species (ROS). Meanwhile, the resin exhibited excellent self-remineralization behavior in an SBF solution, and the molar ratio of Ca/P was close to that of HA. Moreover, the relative growth rate (RGR) of mouse fibroblast L929 indicated a high biocompatibility, with the cytotoxicity level being 0 or I. Therefore, our research provides a suitable approach for improving the antibacterial and mineralization properties of DRCs.Keywords:dental resin composite;dental caries;secondary caries;titanium dioxide;antibacterial property;remineralization
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INTERNATIONAL JOURNAL OF THERMOPHYSICS
·
2023
·Vol. 44
·期 4
·1-25
·
IF 2.2
Liang Ximei,Yang Jian,Meng Xianyang,Wu Jiangtao
A vibrating-wire apparatus was used to measure liquid density and viscosity simultaneously under high-temperature conditions. Densities and viscosities were measured along 11 isotherms at temperatures from (298.15 to 548.15) K and pressures up to 10 MPa for n -dodecane, and over a temperature range of (303.15 to 548.15) K and at equilibrium pressures up to about 6 MPa for carbon dioxide + n -dodecane. The estimated combined expanded uncertainties are 0.24 % for density and 2.2 % for viscosity with a confidence level of 0.95 ( k = 2). In addition, experimental density and viscosity data were correlated with the modified Tait equation and Tait–Andrade equation, respectively, and comparisons with literature data were made. With regard to n -dodecane, the equations present both literature data and our experimental results with deviations almost within 0.2 % for density, and 3.0 % for viscosity. For simplicity, the experimental data of carbon dioxide + n -dodecane were correlated using these two Tait-like equations directly without considering the mole fraction of CO 2 . Both correlations describe our measured data of carbon dioxide + n -dodecane almost within 0.2 % for density and 1 % for viscosity. Graphical Abstract
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2022
·
IF 9.136
Shengnan Lu,Yonghou Xiao,Qidong Zhao,Wenkai Zhao,Gaohong He
Deep desulfurization from fuel has gradually become a research hotspot with enhancing requirements of environmental protection. CPO-27-Ni was considered as one of promising adsorbents towards adsorption desulfurization by virtue of its prodigious high pore volume and high specific surface area. However, the dominant microporous channels in traditional CPO-27-Ni hinder the diffusion of thiophene sulfide and its derivatives with relatively large molecular size, which limits its desulfurization efficiency. Herein, we proposed a strategy to reasonably construct defective CPO-27-Ni with micro-mesoporous structure using N , N -dimethyloctadecylamine (DMA18) as a template, aim at improving the diffusion efficiency by introducing meso -pores. Different amounts of DMA18 were introduced to synthesize defective CPO-27-Ni (DMA18-C- X ) by solvothermal method, and DMA18-C-0.5 (the mole ratio of added DMA18 to Ni 2+ was 0.5) exhibited a satisfactory desulfurization performance. The dynamic breakthrough adsorption capacities of dibenzothiophene, benzothiophene and thiophene over the DMA18-C-0.5 were remarkably promoted, which were as high 3.79, 6.45 and 9.29 times as the traditional CPO-27-Ni, respectively. The crystal structure of CPO-27-Ni was not altered after adding template agent DMA18, while a uniform distribution of mesopores appeared. The largest mesopore attained a size of 2.8 nm, which effectively promoted the full exposure of more unsaturated Ni 2+ active sites and enhanced the interaction between Ni 2+ active sites and sulfides, resulting in strengthened adsorption desulfurization performance. This method of introducing proper defects to construct mesopores in MOFs provides some useful references for preparing high-efficiency desulfurization adsorbents.
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COMBUSTION SCIENCE AND TECHNOLOGY
·
2022
·
IF 2.133
Fanggang Zhang,Yilun Liang,Juan Wang
Nano-sized Co3O4 is an effective catalyst for fuel oxidation due to its high capacity of oxygen storage, and it is thus frequently applied in improving the oxidation performance of hydrocarbon fuels. In our present work, attempts were made to study the catalytic performance of Co3O4 for the oxidation of liquid fuels over a wide temperature range. Neat n-decane and n-decane/1,2,4-trimethylbenzene mixtures were chosen because they are typical liquid hydrocarbon fuels. The evidences from this study suggest that the temperatures of both fuel ignition and full conversion are significantly decreased by Co3O4 catalyst. CO2 is the only product detected in the catalytic oxidation, which also proves the complete oxidation of the liquid fuels. Furthermore, to explore the possible reaction pathways on the catalyst surface, temperature-dependent and time-dependent in situ DRIFTS were employed to identify surface species and analyze catalytic mechanism. Various surface intermediates including bidentate, monodentate carbonate species, carboxylate species and molecular adsorbed n-decane have been observed. The experimental results indicate that n-decane oxidation over Co3O4 proceeds via the Mars-van Krevelen mechanism where lattice oxygen plays a critical role in the fuel oxidation.
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APPLIED SURFACE SCIENCE
·
2022
·
IF 7.392
Qian Zhang,Si Chen,Zhi Huang,Yanying Liu,Jun-ming Hong
Nitrogen atom doping can effectively improve the electrocatalytic performance of graphene materials, and different nitrogen species play various roles. At present, high calcination temperature is commonly used to promote the production of graphitic N. To realize the oriented low-temperature doping of nitrogen atoms in graphene structure, we used O 3 -annealing method in this study to successfully prepare high-content graphitic N doped graphene oxide at 200 °C. Characterization results revealed that O 3 -annealing method can effectively promote the doping of N and O atoms. In addition, O 3 -annealing creating large amount defects for graphene, which directionally promoted the formation of graphitic N (reach 96.82%), which positively affected the improvement of material electrocatalytic properties. The results of bisphenol A (BPA) electrocatalytic degradation by O 3 -5 min-60 °C NGO showed that the degradation efficiency of BPA can reach 100% in 50 min under optimal conditions. The main active substances, namely O 2 − and 1 O 2 were probably generated from the edge oxygen functional groups (O-C=O and C=O) of the materials. BPA underwent a series of reactions, and was finally mineralized to CO 2 and H 2 O. This study provides a new strategy for the directional preparation of high content graphitic N doped graphene oxide for practical application.
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SYNTHETIC COMMUNICATIONS
·
2022
·
IF 1.937
Jinchen Yang,Ling Chen,Yibo Dong,Jinli Zhang,Yangjie Wu
ABATRACTA direct approach to N,N′-disubstituted urea/thiourea from the self-condensation reactions of isothiocyanates in water has been developed. This access tolerated a wide range of functional groups on the aromatic ring, providing a practical and environment-friendly process to N,N′-disubstituted urea/thiourea in moderate to excellent yields from safe and easily available starting materials. A plausible mechanism of the desulfurization self-condensation reaction for urea was also proposed and the role of di-tert-butyl peroxide (DTBP) and copper catalyst in the present strategy was demonstrated with the help of ESI mass spectrometry of intermediate studies.
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BIOORGANIC & MEDICINAL CHEMISTRY
·
2016
·
IF 2.923
Honglei Xie,Yiqun Li,Changlin Bai,Ruifeng Wang,Chunchi Liu,Chenzhou Hao,Bin Lin,Maosheng Cheng,Dongmei Zhao
Epidemiological studies have identified that the risk of cardiovascular events increases due to the decreased levels of high density lipoprotein-cholesterol and the elevated levels of low density lipoprotein-cholesterol. Herein, we report a novel series of N , N -3-phenyl-3-benzylaminopropionanilide derivatives, which were identified as potent cholesteryl ester transfer protein (CETP) inhibitor. The initial lead compound L10 (IC 50 8.06 μM) was found by pharmacophore-based virtual screening (Dong-Mei Zhao et al., Chin. Chem. Lett. 2014 , 25 , 299). After systematic structure variation and biological testing against CETP, two different series were identified as scaffolds for potent CETP inhibitors. One is N , N -3-phenyl-3-benzylaminopropanamide derivatives, which were investigated in our previous paper ( Bioorg. Med. Chem. 2015 , doi: http://dx.doi.org/10.1016/j.bmc.2015.12.010 ). The most potent compound HL16 in that series has the IC 50 of 0.69 μM. The other series is N , N -3-phenyl-3-benzylaminopropionanilide derivatives, which was investigated in current study. Further optimization of the structure–activity relationship (SAR) resulted in H16 (IC 50 0.15 μM), which was discovered as a potent CETP inhibitor in vitro by BODIPY-CE fluorescence assay . In addition, the results of pharmacodynamics studies showed that H16 exhibited both favorable HDL-C enhancement and LDL-C reduction in vivo by hamster. It also has an excellent stability in rat liver microsomal.
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