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Superhydrophobic and corrosion-resistant siloxane-modified MgAl-LDHs coatings on magnesium alloy prepared under mild conditions

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International Journal of Minerals,Metallurgy and Materials 2025年第2期32卷 450-463页

作者： Wenxi Zhang Zhangzelong Zhuo Dan Xu Liang Wu Zhihui Xie Chemical Synthesis and pollution control key laboratory of Sichuan Province College of Chemistry and Chemical EngineeringChina West Normal UniversityNanchong 637002China College of Materials Science and Engineering/National Engineering Research Center for Magnesium Alloys Chongqing UniversityChongqing 400044China

We have developed a superhydrophobic and corrosion-resistant LDH-W/PFDTMS composite coating on the surface of Mg *** composite comprised a tungstate-intercalated(LDH-W)underlayer that was grown at low temperature(relative to hydrothermal reaction conditions)under atmospheric pressure and an outer polysiloxane layer created from a solution containing perfluorodecyltrimethoxysilane(PFDTMS)using a simple immersion *** successful intercalation of tungstate into the LDH phase and the following formation of the polysiloxane layer were confirmed through X-ray diffraction(XRD),Fourier transform infrared(FTIR)spectroscopy,and X-ray photoelectron spectroscopy(XPS).The corrosion resistance of the LDH-W film,both before and after the PFDTMS modification,was evaluated using electrochemical impedance spectroscopy(EIS),Tafel curves,and immersion *** results showed that Mg coated with LDH-W/PFDTMS exhibited significantly enhanced corrosion protection compared to the unmodified LDHW film,with no apparent signs of corrosion after exposure to 3.5wt%NaCl solution for 15 ***,the LDH-W/PFDTMS coating demonstrated superior superhydrophobicity and self-cleaning properties against water and several common beverages,as confirmed by static contact angle and water-repellency *** results offer valuable insights into preparing superhydrophobic and corrosion-resistant LDH-based composite coatings on Mg alloy surfaces under relatively mild reaction conditions.

关键词： Mg alloy corrosion coating layered double hydroxide

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Catalyst–Support Interaction in Polyaniline‑Supported Ni_(3)Fe Oxide to Boost Oxygen Evolution Activities for Rechargeable Zn‑Air Batteries

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Nano-Micro Letters 2025年第1期17卷 176-190页

作者： Xiaohong Zou Qian Lu Mingcong Tang Jie Wu Kouer Zhang Wenzhi Li Yunxia Hu Xiaomin Xu Xiao Zhang Zongping Shao Liang An Department of Mechanical Engineering The Hong Kong Polytechnic UniversityHung HomKowloonHong Kong SARPeople’s Republic of China Jiangsu key laboratory of atmospheric environment monitoring and pollution control Jiangsu Collaborative Innovation Center of Atmospheric Environment and Equipment TechnologySchool of Environmental Science and TechnologyNanjing University of Information Science and TechnologyNanjing 210044People’s Republic of China Department of Chemistry The Chinese University of Hong KongMa Lin BuildingShatinHong Kong SAR 999077People’s Republic of China WA School of Mines:Minerals Energy and Chemical Engineering(WASM‑MECE)Curtin UniversityPerthWA 6102Australia Research Institute for Advanced Manufacturing The Hong Kong Polytechnic UniversityHung HomKowloonHong Kong SARPeople’s Republic of China Research Institute for Smart Energy The Hong Kong Polytechnic UniversityHung HomKowloonHong Kong SARPeople’s Republic of China

Catalyst–support interaction plays a crucial role in improving the catalytic activity of oxygen evolution reaction(OER).Here we modulate the catalyst–support interaction in polyaniline-supported Ni_(3)Fe oxide(Ni_(3)Fe oxide/PANI)with a robust hetero-interface,which significantly improves oxygen evolution activities with an overpotential of 270 mV at 10 mA cm^(-2)and specific activity of 2.08 mA cm_(ECSA)^(-2)at overpotential of 300 mV,3.84-fold that of Ni_(3)Fe *** is revealed that the catalyst–support interaction between Ni_(3)Fe oxide and PANI support enhances the Ni–O covalency via the interfacial Ni–N bond,thus promoting the charge and mass transfer on Ni_(3)Fe *** the excellent activity and stability,rechargeable Zn-air batteries with optimum Ni_(3)Fe oxide/PANI are assembled,delivering a low charge voltage of 1.95 V to cycle for 400 h at 10 mA cm^(-2).The regulation of the effect of catalyst–support interaction on catalytic activity provides new possibilities for the future design of highly efficient OER catalysts.

关键词： Catalyst-support interaction Supported catalysts Heterointerface Oxygen evolution reaction Zn-air batteries

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Seasonal variations, temperature dependence, and sources of size-resolved PM components in Nanjing, east China

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Journal of environmental Sciences 2022年第11期34卷 175-186页

作者： Mingjie Xie Wei Feng Shuyan He Qin’geng Wang Collaborative Innovation Center of atmospheric environment and Equipment Technology Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution ControlSchool of Environmental Science and EngineeringNanjing University of Information Science&TechnologyNanjing 210044China State key laboratory of pollution control and Resources Reuse School of the EnvironmentNanjing UniversityNanjing 210023China

Size-segregated ambient particulate matter(PM) samples were collected seasonally in suburban Nanjing of east China from 2016 to 2017 and chemically speciated. In both fine( 2.1 μm, PM>2.1) PM, organic carbon(OC) accounted for the highest fractions(26.9% ± 10.9% and 23.1% ± 9.35%) of all measured species, and NO3-lead in average concentrations of water-soluble inorganic ions(WSIIs). The size distributions of measured components were parameterized using geometric mean diameter(GMD). GMD values of NO_(3)^(-), Cl^(-), OC, and PM for the whole size range varied from 2.1μm in warm seasons, which was due to the fact that the size distributions of semi-volatile components(e.g., NH4NO3, NH4Cl, and OC) had a dependency on the ambient *** OC, elemental carbon(EC), and elements, NH_(4)^(+), NO_(3)^(-), and SO_(4)^(2-)exhibited an increase trend in GMD values with relative humidity, indicating that the hygroscopic growth might also play a role in driving seasonal changes of PM size distributions. Positive matrix factorization was performed using compositional data of fine and coarse particles, respectively. The secondary formation of inorganic salts contributing to the majority(> 70%) of fine PM and 20.2% ± 19.9% of speciated coarse PM. The remaining coarse PM content was attributed to a variety of dust sources. Considering that coarse and fine PM had comparable mass concentrations, more attention should be paid to local dust emissions in future air quality plans.

关键词： Particulate matter Size distribution Seasonal variation Semi-volatility Source apportionment

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Effect of sulfate on Cu(Ⅱ)sorption to polymer-supported nano-hydrated ferric oxides:Experimental and modeling studies

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Chinese Journal of Chemical Engineering 2021年第5期34卷 319-326页

作者： Wenxiang Ni Luyang Yang Xiaolin Zhang Hui Qiu Collaborative Innovation Center of atmospheric environment and Equipment Technology Jiangsu Key Laboratory of Atmospheric Environment Monitoring and PollutionControlSchool of Environmental Science and EngineeringNanjing University of Information Science&TechnologyNanjing 210044China State key laboratory of pollution control and Resource Reuse School of the EnvironmentNanjing UniversityNanjing 210023China

Incorporating of hydrous ferric oxide(HFO)inside porous supports with large sizes has become an effective way to decontaminate the water from heavy *** anions like sulfate are usually present in high concentrations in water,and might greatly affect adsorption behavior of hybrid ***,a polymer-based HFO-CPS was fabricated by encapsulating nano-HFO inside a chloromethylated polystyrene polymer(CPS)and the reactivity of HFO-CPS with Cu(Ⅱ)was evaluated in the presence of sulfate *** complexation theory was firstly employed to describe the effect of sulfate on Cu(Ⅱ)adsorption edges of hybrid HFO-CPS,where constant capacitance model(CCM)was *** available weak adsorption site Fe_((2))OH of hybrid HFO-CPS was found to decrease from 20% Fe to 5% Fe,which might be caused by the pore plugging effect after HFO *** the assumption that a ternary complex was formed,the effect of sulfate on Cu(Ⅱ)adsorption by HFO-CPS were successfully described by CCM using the optimized Fe_((2))OH site under different sulfate concentrations(1 or 10 mmol·L^(-1))and Cu/Fe ratios(0.0042 or 0.0252).It is confirmed that the formation of FeOHCuSO4 ternary surface complexes played an important role in enhancing Cu(Ⅱ)adsorption on HFO-CPS in the presence of sulfate.

关键词： Iron oxides Polymer Sulfate Adsorption Ternary complex

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Theoretical insights of the pharmaceutical compound fluoxetine in water:Role in direct photolysis and indirect photolysis by free radicals

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Journal of environmental Sciences 2024年第8期142卷 269-278页

作者： Ying Lu Se Wang Yifan Shen School of environmental Science and Engineering Collaborative Innovation Center of Atmospheric Environment and Equipment TechnologyJiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution ControlNanjing University of Information Science and TechnologyNanjing 210044China

The frequent detection of pharmaceutical compounds in the environment has led to a growing awareness,which may pose a major threat to the aquatic *** this study,photodegradation(direct and indirect photolysis)of two different dissociation states of fluoxetine(FLU)was investigated in water,mainly including the determination of photolytic transition states and products,and the mechanisms of indirect photodegradation with·OH,CO_(3)^(*-)and NO_(3)^(*).The main direct photolysis pathways are defluorination and C–C bond *** addition,the indirect photodegradation of FLU in water is mainly through the reactions with·OH and NO_(3)^(*),and the photodegradation reaction with CO_(3)^(*-)is relatively difficult to occur in the water *** results provide a theoretical basis for understanding the phototransformation process of FLU in the water environment and assessing its potential risk.

关键词： Fluoxetine Photochemical mechanism Direct photolysis Free radical reaction DFT

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Crystal Structure and Theoretical Energy Gap of 2-(2-((4-(Pyridin-2-yl)pyrimidin-2-yl)disulfanyl)pyrimidin-4-yl)pyridinium Hexafluorophosphate

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Chinese Journal of Structural Chemistry 2017年第2期36卷 229-235页

作者：陶涛赵煚珖曹晖 Jiangsu key laboratory of atmospheric environment monitoring and pollution control Collaborative Innovation Center of Atmospheric Environment and Equipment TechnologySchool of Environmental Science and Engineering Nanjing University of Information Science &Technology

The crystal structure of 2-（2-（（4-（pyridin-2-yl）pyrimidin-2-yl）disulfanyl）pyrimidin-4-yl）pyridinium hexafluorophosphate was obtained by X-ray single-crystal diffraction. This molecule crystallizes in monoclinic P2/c space group with a=6.219（1）, b=13.103（2）, c=13.059（2） , β=97.567（2）°, Z=2, the final R=0.0525 and w R=0.1434. The title compound was prepared successfully from 1,2-bis（4-（pyridin-3-yl）pyrimidin-2-yl）disulfane（BPPD）. TD-DFT computational studies on energy gaps and UV-Vis spectra of BPPD and the title compound have been carried out for comparisons. The resultant HOMO-LUMO gap of the BPPD compound is 4.45 e V, while that for the corresponding hexafluorophosphate salt is much smaller at 2.46 e V, which are in agreement with their UV-Vis absorptions.

关键词： resultant monoclinic pyrimidine torsion assembly conjugated octahedral salts heterocyclic tetra

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Microphysical Characteristics of Sea Fog over the East Coast of Leizhou Peninsula, China

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Advances in atmospheric Sciences 2013年第4期30卷 1154-1172页

作者：赵丽娟牛生杰张羽徐峰 Jiangsu key laboratory of atmospheric environment monitoring and pollution control School of Atmospheric Physics Nanjing University of Information Science and Technology Zhanjiang Meteorological Bureau Guangdong Ocean University

Microphysical properties of sea fog and correlations of these properties were analyzed based on the measurements from a comprehensive field campaign carried out from 15 March to 18 April 2010 on Donghai Island （21°35″N, 110°32″5′E） in Zhanjiang, Guangdong Province, China. There were four types of circula- tion pattern in favor of sea fog events in this area identified, and the synoptic weather pattern was found to influence the microphysical properties of the sea fogs. Those influenced by a warm sector in front of a cold front or the anterior part of low pressure were found to usually have a much longer duration, lower visibility, greater liquid water content, and bigger fog droplet sizes. A fog droplet number concentration of N≥1 cm-a and liquid water content of L≥0.001 g m-a can be used to define sea fogs in this area. The type of fog droplet size distribution of the sea fog events was mostly monotonically-decreasing, with the spectrum width always being 〉20 μm. The significant temporal variation of N was due in large part to the number concentration variation of fog droplets with radius 〈3 μm. A strong collection process appeared when droplet spectrum width was 〉10 μm, which subsequently led to the sudden increase of droplet spectrmn width. The doln- inant physical process during the sea fog events was activation with subsequent condensational growth or reversible evaporation processes, but turbulent mixing also played an important role. The collection process occurred, but was not vital.

关键词： microphysical property microphysical correlation fog droplet size distribution the South China Sea

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^(18)F-Labeling techniques for positron emission tomography

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Science China Chemistry 2013年第12期56卷 1682-1692页

作者： LI Ying Jiangsu key laboratory of atmospheric environment monitoring & pollution control Chemistry Department School of Environmental Science & Engineering Nanjing University of Information Science & Technology

Much research effort has been made to understand various biological processes at levels of molecules using molecular imaging techniques. Because of great sensitivity, high resolution, and rapid detection, positron emission tomography （PET） imaging is becoming one of the most used imaging techniques for medical diagnose and pre-clinical studies. Here we provide a review on molecular imaging and PET imaging. An introduction is also provided on ~SF-fluorine labeling techniques for the preparation of PET imaging probes. A summary and comparison of currently available ~SF-fluorine labeling methods is provided. The per- spectives for 18F-fluorine labeling techniques are also given.

关键词： molecular imaging positron emission tomography 18F-fluorine/fluoride specific activity radiochemical yield

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Molten-salt synthesis and composition-dependent luminescent properties of barium tungsto-molybdate-based solid solution phosphors

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Chinese Physics B 2016年第2期25卷 482-488页

作者：贺香红叶招莲关明云连宁孙建华 School of Chemistry and environmental Engineering Jiangsu University of Technology Jiangsu key laboratory of atmospheric environment monitoring and pollution control (AEMPC) School of Environment Science and EngineeringNanjing University of Information Science and Technology

Pr^（3＋）-activated barium tungsto-molybdate solid solution phosphor Ba（Mo_（1-z）W_z）O_4：Pr^（3＋）is successfully fabricated via a facile molten-salt approach. The as-synthesized microcrystal is of truncated octahedron and exhibits deep-red-emitting upon blue light excitation. Powder x-ray diffraction and Raman spectroscopy techniques are utilized to investigate the formation of solid solution phosphor. The luminescence behaviors depend on the resulting composition of the microcrystals with fixed Pr^（3＋）-doping concentration, while the host lattices remain in a scheelite structure. The forming solid solution via the substitution of [WO_4] for [MoO_4] can significantly enhance its luminescence, which may be due to the fact that Ba（Mo_（1-z）W_z）O_4：Pr^（3＋）owns well-defined facets and uniform morphologies. Owing to its properties of high phase purity,well-defined facets, highly uniform morphologies, exceptional chemical and thermal stabilities, and stronger emission intensity, the resulting solid solution phosphor is expected to find potential applications in phosphor-converted white lightemitting diodes（LEDs）.

关键词： molten-salt barium tungsto-molybdate microcrystals solid solution deep-red-emitting

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Contrasting trends of PM2.5 and surface-ozone concentrations in China from 2013 to 2017

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National Science Review 2020年第8期7卷 1331-1339页

作者： Yonghong Wang Wenkang Gao Shuai Wang Tao Song Zhengyu Gong Dongsheng Ji Lili Wang Zirui Liu Guiqian Tang Yanfeng Huo Shili Tian Jiayun Li Mingge Li Yuan Yang Biwu Chu Tuukka Pet?j? Veli-Matti Kerminen Hong He Jiming Hao Markku Kulmala Yuesi Wang Yuanhang Zhang State key laboratory of atmospheric Boundary Layer Physics and atmospheric Chemistry (LAPC) Institute of Atmospheric Physics Chinese Academy of Sciences Institute for atmospheric and Earth System Research University of Helsinki China National environmental monitoring Center (CNEMC) Anhui Institute of Meteorological Sciences State key Joint laboratory of environment Simulation and pollution control Research Center for Eco-Environmental Sciences Chinese Academy of Sciences Center for Excellence in Regional atmospheric environment Institute of Urban Environment Chinese Academy of Sciences State key Joint laboratory of environment Simulation and pollution control School of Environment Tsinghua University State key Joint laboratory of environmental Simulation and pollution control College of Environmental Sciences and Engineering Peking University

Although much attention has been paid to investigating and controlling air pollution in China, the trends of air-pollutant concentrations on a national scale have remained unclear. Here, we quantitatively investigated the variation of air pollutants in China using long-term comprehensive data sets from 2013 to 2017, during which Chinese government made major efforts to reduce anthropogenic emission in polluted regions. Our results show a significant decreasing trend in the PM2.5concentration in heavily polluted regions of eastern China, with an annual decrease of ～7% compared with measurements in 2013. The measured decreased concentrations of SO2, NO2and CO（a proxy for anthropogenic volatile organic compounds） could explain a large fraction of the decreased PM2.5concentrations in different regions. As a consequence, the heavily polluted days decreased significantly in corresponding regions. Concentrations of organic aerosol,nitrate, sulfate, ammonium and chloride measured in urban Beijing revealed a remarkable reduction from 2013 to 2017, connecting the decreases in aerosol precursors with corresponding chemical components closely. However, surface-ozone concentrations showed increasing trends in most urban stations from 2013 to 2017, which indicates stronger photochemical pollution. The boundary-layer height in capital cities of eastern China showed no significant trends over the Beijing–Tianjin–Hebei, Yangtze River Delta and Pearl River Delta regions from 2013 to 2017, which confirmed the reduction in anthropogenic emissions. Our results demonstrated that the Chinese government was successful in the reduction of particulate matter in urban areas from 2013 to 2017, although the ozone concentration has increased significantly, suggesting a more complex mechanism of improving Chinese air quality in the future.

关键词： air pollution clean-air action particulate matter surface ozone China chemical composition

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