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Journal of Environmental Sciences 2024年第5期139卷 245-257页

作者： Chaomin Jia Jianbing Wang Huijiao wang Sichao Zhu Xiaohui Zhang Yuxiang wang School of Chemical&Environmental Engineering China University of Mining&Technology-BeijingBeijing 100083China Beijing Polytechnic Beijing 100176China Chinese Society for Urban Studies Beijing 100835China

Water fluoride pollution has caused non-negligible harm to the environment and humans,and thus it is crucial to find a suitable treatment technology.In this study,La-Fe@PTA adsorbent was synthesized for the defluoridation of mine water.The results showed that the optimum conditions for defluoridation by La-Fe@PTA were p H close to 7.0,the initial F-concentration of 10 mg/L,the dosage of 0.5 g/L and the adsorption time of 240 min.Compared with SO_4^(2-),Cl^(-),NO_(3)^(-),Ca^(2+)and Mg^(2+),CO_(3)^(2-)and HCO_(3)^(-)presented severer inhibition on fluoride uptake by La-Fe@PTA.The adsorption process fits well with the pseudo-second-order kinetic model and Freundlich model,and the maximum adsorption capacity of Langmuir model was 95 mg/g.Fixed-bed adsorption results indicated that fluoride in practical fluorinated mine water could be effectively removed from 3.6 mg/L to less than 1.5 mg/L within130 bed volume(BV)by using 1.5 g La-Fe@PTA.Furthermore,the adsorbent still had good adsorption capacity after regeneration,which confirms the great application potential of La-Fe@PTA as a fluoride ion adsorbent.The mechanism analysis showed that La-Fe@PTA adsorption of fluorine ions is a physicochemical reaction driven by electrostatic attraction and ion exchange.

关键词： Adsorption La-Fe@PTA Fluoride ion Mine water Mechanism

Genome-Wide Analysis of the F3′5′H Gene Family in Blueberry(Vaccinium corymbosum L.)Provides Insights into the Regulation of Anthocyanin Biosynthesis

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Phyton-International Journal of Experimental Botany 2023年第9期92卷 2683-2697页

作者： Xiaolan Guo Jinbin Hu Shimei Yang Delu wang Jianbing Wang College of Life Sciences Huizhou UniversityHuizhou516007China College of Forestry Guizhou UniversityGuiyang550025China School of Architecture and Civil Engineering Huizhou UniversityHuizhou516007China Guizhou Institute of Subtropical Crop. Guizhou Academy of Agricultural SciencesXingyi562400China

The F3′5′H gene family plays an important role in regulating anthocyanin biosynthesis,abiotic stress,and hormone signaling.In this study,14 F3′5′H genes were identified from the blueberry genome.The chromosomal distribution,physicochemical properties,F3′5′H domain,conserved motifs,cis-acting elements,and intron/exon compositions were analyzed.The functional prediction analysis of these VcF3′5′Hs indicated that their biological functions included light response and other secondary metabolites.The results of qRT-PCR showed that VcF3′5′Hs(especially VcF3′5′H4)were highly expressed at the ripening stage.Subcellular localization revealed that VcF3′5′H4 may be located in the endoplasmic reticulum.Co-expression analysis showed that the VcF3′5′H gene family was related to anthocyanin.This research provides an overview of the blueberry F3′5′H family and helps verify the role of these genes in regulating anthocyanin biosynthesis.

关键词： Blueberry F3′5′H anthocyanin gene expression co-expression

Enhanced triallyl isocyanurate(TAIC)degradation through application of an 03/UV process:Performance optimization and degradation pathways

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Frontiers of Environmental Science & Engineering 2020年第4期14卷 103-113页

作者： Yapeng Song Hui Gong Jianbing Wang Fengmin Chang Kaijun wang State Key Joint Laboratory of Environment Simulation and Pollution Control School of EnvironmentTsinghua UniversityBeijing 100084China School of Chemical&Environmental Engineering China University of Mining and TechnologyBeijing 100083China

Triallyl isocyanurate(TAIC,C12H15N3O3)has featured in wastewater treatment as a refractory organic compound due to the significant production capability and negative environmental impact.TAIC degradation was enhanced when an ozone(O3)/ultraviolet(UV)process was applied compared with the application of an independent O3 process.Although 99%of TAIC could be degraded in 5 min during both processes,the O3/UV process had a 70%mineralization rate that was much higher than that of the independent O3 process(9%)in 30 min.Four possible degradation pathways were proposed based on the organic compounds of intermediate products identified during TAIC degradation through the application of independent 03 and O3/UV processes.pH impacted both the direct and indirect oxidation processes.Acidic and alkaline conditions preferred direct and indirect reactions respectively,with a pH of 9 achieving maximum Total Organic Carbon(TOC)removal.Both CO32-and HCO3-decreased TOC removal,however only CO32-negatively impacted TAIC degradation.Effects of Cl-as a radical scavenger became more marked only at high concentrations(over 500 mg/L Cl-).Particulate and suspended matter could hinder the transmission of ultraviolet light and reduce the production of HO·accordingly.

关键词： Triallyl isocyanurate O3/UV Advanced oxidation processes(AOP) Degradation pathway

Research progress of CO_(2) capture and mineralization based on natural minerals

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International Journal of Minerals,Metallurgy and Materials 2024年第6期31卷 1208-1227页

作者： Chenguang Qian Chunquan Li Peng Huang Jialin Liang Xin Zhang Jifa wang Jianbing Wang Zhiming Sun School of Chemical and Environmental Engineering China University of Mining and Technology(Beijing)Beijing 100083China Shanghai Construction Building Material Technology Group Shanghai 200080China

Natural minerals,such as kaolinite,halloysite,montmorillonite,attapulgite,bentonite,sepiolite,forsterite,and wollastonite,have considerable potential for use in CO_(2) capture and mineralization due to their abundant reserves,low cost,excellent mechanical prop-erties,and chemical stability.Over the past decades,various methods,such as those involving heat,acid,alkali,organic amine,amino sil-ane,and ionic liquid,have been employed to enhance the CO_(2) capture performance of natural minerals to attain high specific surface area,a large number of pore structures,and rich active sites.Future research on CO_(2) capture by natural minerals will focus on the full utiliza-tion of the properties of natural minerals,adoption of suitable modification methods,and preparation of composite materials with high specific surface area and rich active sites.In addition,we provide a summary of the principle and technical route of direct and indirect mineralization of CO_(2) by natural minerals.This process uses minerals with high calcium and magnesium contents,such as forsterite(Mg_(2)SiO_(4)),serpentine[Mg_(3)Si_(2)O(OH)_(4)],and wollastonite(CaSiO_(3)).The research status of indirect mineralization of CO_(2) using hydro-chloric acid,acetic acid,molten salt,and ammonium salt as media is also introduced in detail.The recovery of additives and high-value-added products during the mineralization process to increase economic benefits is another focus of future research on CO_(2) mineralization by natural minerals.

关键词： natural mineral carbon dioxide capture modification composite material carbon dioxide mineralization

Adsorptive removal of antibiotics from water using magneticion exchange resin

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Journal of Environmental Sciences 2017年第2期29卷 111-117页

作者： Tianyue wang Xun Pan Weiwei Ben Jianbing Wang Pin Hou Zhimin Qiang Key Laboratory of Drinking Water Science and Technology Research Center for Eco-Enuironmental SciencesChinese Academy of SciencesBeijing 100085China School of Chemical and Enuironmental Engineering Beijing CampusChina University of Mining and TechnologyBeijing 100083China Foreign Economic Cooperation Office Ministry of Environmental ProtectionBeijing 100035China

The occurrence of antibiotics in the environment has recently raised serious concern regarding their potential threat to aquatic ecosystem and human health. In this study, the magnetic ion exchange（MIEX） resin was applied for removing three commonly-used antibiotics, sulfamethoxazole（SMX）, tetracycline（TCN） and amoxicillin（AMX） from water.The results of batch experiments show that the maximum adsorption capacities on the MIEX resin for SMX, TCN and AMX were 789.32, 443.18 and 155.15 μg/m L at 25°C,respectively, which were 2–7 times that for the powdered activated carbon. The adsorption kinetics of antibiotics on the MIEX resin could be simulated by the pseudo-second-order model（R^2= 0.99）, and the adsorption isotherm data were well described by the Langmuir model（R^2= 0.97）. Solution p H exhibited a remarkable impact on the adsorption process and the absorbed concentrations of the tested antibiotics were obtained around the neutral p H.The MIEX resin could be easily regenerated by 2 mol/L Na Cl solution and maintained high adsorption removal for the tested antibiotics after regeneration. Anion exchange mechanism mainly controlled the adsorption of antibiotic and the formation of hydrogen binding between the antibiotic and resin can also result in the increase of adsorption capacity. The high adsorption capacity, fast adsorption rate and prominent reusability make the MIEX resin a potential adsorbent in the application for removing antibiotics from water.

关键词： Sulfamethoxazole Tetracycline Amoxicillin Antibiotics MIEX resin Adsorption

Treatment of coking wastewater using oxic-anoxic-oxic process followed by coagulation and ozonation

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Carbon Resources Conversion 2019年第2期2卷 151-156页

作者： Jianbing Wang Yuxian Ji Fengyuan Zhang Dongliang wang Xuwen He Chunrong wang School of Chemical and Environmental Engineering China University of Mining and Technology-BeijingBeijing 100083China

An oxic-anoxic-oxic(O-A-O)system followed by coagulation and ozonation processes was used to study the treatment of coking wastewater.In the O-A-O process,the removals of NH4+-N,total nitrogen and COD were 91.5-93.3%,91.3-92.6%and 89.1-93.8%,respectively when employing hydraulic residence times of 60 h for the biochemical system.High removal of NH4+-N was obtained due to the placement of an aerobic tank in front of A-O system which can mitigate the inhibitory effect of toxic compounds in coking wastewater on nitrifying bacteria.Addition of methanol into the anoxic reactor greatly increased the removal of total nitrogen,indicating that denitrifiers can hardly use organic compounds in coking wastewater as carbon source for denitrification.COD values of the effluent from the O-A-O system were still higher than 260 mg/L even with a prolonged time of 160 h mainly due to the high refractory properties of residual compounds in the effluent.The subsequent coagulation and ozonation processes resulted in the COD removal of 91.5%-93.3%and reduced the relative abundance of large molecular weight(MW)organics(>1 kDa)from 55.8%to 20.93%with the ozone,PAC and PAM dosages of 100,150 and 4 mg/L respectively.Under these conditions,the COD value and concentration of polycyclic aromatic hydrocarbons in the final effluent were less than 80 and 0.05 mg/L,respectively,which meet the requirement of the Chinese emission standard.These results indicate that the combined technology of O-A-O process,coagulation and ozonation is a reliable way for the treatment of coking wastewater.

关键词： Coking wastewater Activated sludge process Coagulation Ozonation Nitrification-denitrification

Developing high-quality g-C_(3)N_(4) film electrode for the photoelectrocatalytic degradation of methylene blue in water

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Chinese Chemical Letters 2023年第3期34卷 175-180页

作者： Yanxi Gong Jianbing Wang Zikun Cheng Zhiyuan Han Xu Zhao Buyu Chai Yuanchun Han China University of Mining and Technology-Beijing Beijing 100083China Research Center for Eco-Environment Sciences Chinese Academy of SciencesBeijing 100085China

Developing a high-quality photoelectrode for photoelectrochemical applications is still an ongoing challenge. In this study, we prepared the g-C_(3)N_(4) film on the indium tin oxide(ITO) glass through conventional coating, liquid-based growth, in-situ calcination, and vapor deposition methods, respectively. These electrodes were characterized and used as photoanodes to degrade methylene blue(MB) in water. Among these methods, the in-situ calcination method was most appropriate for preparing the continuous and organized g-C_(3)N_(4) film electrodes with uniform g-C_(3)N_(4) coverage and strong adhesion to the ITO substrate.It also had the highest activity in the photocatalytic(PC), electrochemical(EC), and photoelectrocatalytic(PEC) degradation processes of MB. In the PEC reaction, at an applied potential of 1.0 V and a light intensity of 0.96 W/cm^(2), the removal rate of MB was 62.5%, which was much higher than those in the PC and EC reactions. The high degradation rate was due to the synergistic effect of PEC degradation, wherein the PC and EC reactions promote and optimize each other. In the PC reaction, MB was degraded by-CH_(3) elimination, while the EC degradation pathway mainly included the conversion of sulfhydryl into sulfoxide and the opening of the central aromatic ring. Both methyl loss and aromatic ring opening occurred in the PEC reaction. Moreover, some monocyclic compounds were formed, and MB showed more complete degradation in the PEC reaction.

关键词： Graphitic carbon nitride Photoelectrochemical activity Methylene blue Degradation pathway Synergistic effect

Structural design of the fluted shaped charge liner using multi-section optimization method

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Defence Technology(防务技术) 2023年第7期25卷 249-262页

作者： Shengjie Sun Jianwei Jiang Shuyou wang jianbing Men Mei Li State Key Laboratory of Explosion Science and Technology Beijing Institute of TechnologyBeijing 100081PR China Tangshan Research Institute Beijing Institute of TechnologyTangshan 063000HebeiPR China

Spin effect of the small diameter shaped charge results in the centrifugal stress during the jet stretching process. Consequently, the jet scatters, which deceases the jet penetration capability. In the present study, a multi-section method was proposed to design the spin-compensation liner. The spincompensation rate(SCR) of the liner was defined as the specific angular velocity that a fluted liner can offset. Based on the plain stress theory, SPH numerical method was applied to study the converging process of the 2D fluted structure. The spin-compensation mechanism of the fluted structure was illustrated. Then, nine cross sections were chosen along the liner axis equidistantly. On each of the section, a 2D fluted structure was designed to offset a given initial angular velocity. After, the optimized fluted structures were integrated into a 3D fluted liner. Jet appearances of the normal liner and the fluted liners under different initial angular velocities were compared, which verifies the practicality of the multi-sectional method. The multi-section optimization method provides a new efficient method of designing the shaped charge liner for a specific usage.

关键词： Fluted liner Spin-compensation SPH Structural optimization

Redox flow batteries based on insoluble redox-active materials.A review

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Nano Materials Science 2021年第1期3卷 17-24页

作者： Xiao wang Jingchao Chai jianbing“Jimmy”Jiang Department of Chemistry University of CincinnatiP.O.Box 210172CincinnatiOH45221-0172United States

The ever-increasing demand for energy has stimulated the development of economical non-fossil fuels.As representative of clean energy,solar and wind have been identified as the most promising energy sources due to their abundance,cost efficiency,and environmental friendliness.The intrinsic intermittent of the clean energy leads to the urgent requirements large-scale energy storage technique.Redox flow batteries(RFBs)are attractive technology due to their independent control over energy and power.Insoluble redox-active flow battery is a new type of electrochemical energy storage technology that disperses redox-active particles in the electrolyte.Compared with traditional flow batteries,insoluble flow batteries have advantages of large energy density and are very promising in the development of large-scale energy storage systems.At present,three types of insoluble flow batteries have been explored:slurry-based flow batteries,metal/slurry hybrid,and redox-mediator-assisted flow batteries.This Review summarizes the research progress of insoluble flow batteries,and analyzes the key challenges from the fundamental research and practical application perspectives.

关键词： Membrane Redox flow battery Redox mediator Slurry

Catalytic wet air oxidation of phenol with functionalized carbon materials as catalysts:Reaction mechanism and pathway

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Journal of Environmental Sciences 2014年第8期26卷 1741-1749页

作者： Jianbing Wang Wantao Fu Xuwen He Shaoxia Yang Wanpeng Zhu School of Chemical and Environmental Engineering Beijing CampusChina University of Mining and Technology School of Environment Tsinghua University

The development of highly active carbon material catalysts in catalytic wet air oxidation（CWAO）has attracted a great deal of attention. In this study different carbon material catalysts（multi-walled carbon nanotubes,carbon fibers and graphite） were developed to enhance the CWAO of phenol in aqueous solution. The functionalized carbon materials exhibited excellent catalytic activity in the CWAO of phenol. After 60 min reaction,the removal of phenol was nearly100% over the functionalized multi-walled carbon,while it was only 14% over the purified multi-walled carbon under the same reaction conditions. Carboxylic acid groups introduced on the surface of the functionalized carbon materials play an important role in the catalytic activity in CWAO. They can promote the production of free radicals,which act as strong oxidants in CWAO. Based on the analysis of the intermediates produced in the CWAO reactions,a new reaction pathway for the CWAO of phenol was proposed in this study. There are some differences between the proposed reaction pathway and that reported in the literature. First,maleic acid is transformed directly into malonic acid. Second,acetic acid is oxidized into an unknown intermediate,which is then oxidized into CO2 and H2O. Finally,formic acid and oxalic acid can mutually interconvert when conditions are favorable.

关键词： Catalytic wet air oxidation,Phenol,Carbon materials,Radical,Reaction pathway