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Locally Enhanced Flow and Electric Fields Through a Tip Effect for Efficient Flow‑Electrode Capacitive Deionization

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Nano-Micro Letters 2025年第2期17卷 1-17页

作者： Ziquan Wang Xiangfeng Chen Yuan Zhang Jie Ma Zhiqun Lin Amor Abdelkader Maria‑Magdalena Titirici Libo Deng College of Chemistry and environmental Engineering Shenzhen UniversityShenzhen 518060People’s Republic of China Research Center for environmental Functional Materials College of Environmental Science and EngineeringTongji University1239 Siping RoadShanghai 200092People’s Republic of China Department of Chemical and Biomolecular Engineering National University of SingaporeSingapore 117585Singapore Department of Engineering Faculty of Science and TechnologyBournemouth UniversityTalbot CampusFern BarrowPooleEngland BH125BBUK Institut de Chimie de Nice UniversitéCôte d’AzurUMR CNRS 727228 Av.Valrose06108 NiceFrance Department of Chemical Engineering Imperial College LondonSouth Kensington CampusExhibition RdLondon SW72AZUK

Low-electrode capacitive deionization(FCDI)is an emerging desalination technology with great potential for removal and/or recycling ions from a range of ***,it still suffers from inefficient charge transfer and ion transport kinetics due to weak turbulence and low electric intensity in flow electrodes,both restricted by the current ***,a new tip-array current collector(designated as T-CC)was developed to replace the conventional planar current collectors,which intensifies both the charge transfer and ion transport *** effects of tip arrays on flow and electric fields were studied by both computational simulations and electrochemical impedance spectroscopy,which revealed the reduction of ion transport barrier,charge transport barrier and internal *** the voltage increased from 1.0 to 1.5 and 2.0 V,the T-CC-based FCDI system(T-FCDI)exhibited average salt removal rates(ASRR)of 0.18,0.50,and 0.89μmol cm^(-2) min^(-1),respectively,which are 1.82,2.65,and 2.48 folds higher than that of the conventional serpentine current collectors,and 1.48,1.67,and 1.49 folds higher than that of the planar current ***,with the solid content in flow electrodes increased from 1 to 5 wt%,the ASRR for T-FCDI increased from 0.29 to 0.50μmol cm^(-2) min^(-1),which are 1.70 and 1.67 folds higher than that of the planar current ***,a salt removal efficiency of 99.89%was achieved with T-FCDI and the charge efficiency remained above 95%after 24 h of operation,thus showing its superior long-term stability.

关键词： Flow-electrode Capacitive deionization Current collector Tip effect Desalination

Adsorption of arsenate and arsenite from aqueous solutions by cerium-loaded cation exchange resin

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Journal of Rare Earths 2012年第6期30卷 563-572页

作者：何宗良田森林宁平 faculty of environmental science and Engineering Kunming University of Science and Technology

The removal of arsenic from water and wastewater is obligatory. Resin is one of the most effective adsorbents for the removal of arsenic. In order to improve the adsorption capacity of resin, a new cerium-loaded cation exchange resin arsenic adsorbent was prepared by impregnating cerium into the cation exchange resin. Batch adsorption experiments under various conditions, such as time, temperature, pH and with coexisting ions were carried out to evaluate the adsorption characteristics of cerium-loaded resin in the removal of As（V） and As（III） from aqueous solutions. The results showed that the adsorption kinetics of As（V） and As（III） obeyed a pseudo second-order kinetic model and the adsorption rate constants were 0.3159 and 0.5215 ***-1-min-1, respectively. The adsorption of As（V） followed the Freundlich adsorption isotherm model and the adsorption isotherm data for As（III） fitted well to the Langmuir equation model. The adsorption capacities were 1.0278 mg/g for As（V） and 2.5297 mg/g for As（Ill）. Both the adsorption of As（V） and As（Ill） were found to be pH sensitive and the optimum pH was found to be 5-6. Except for the phosphate ion, the coexisting anionics, such as nitrate, chlorate, sulphate and carbonate, showed no remarkable effect on As（V） and As（ill） adsorption. The desorption and regeneration study showed that the adsorption capacity of Ce-loaded resin for As（V） and As（Ill） could be restored to 97.80% and 69.61%, respectively, using 0.5 moFL sodium hydroxide solution.

关键词： arsenic pollution cerium resin arsenate arsenite adsorption rare earths

Photodegradation of 17α-ethynylestradiol in dissolved humic substances solution：Kinetics,mechanism and estrogenicity variation

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Journal of environmental sciences 2017年第4期29卷 196-205页

作者： Dong Ren Bin Huang Dan Xiong Huan He Xiangqi Meng Xuejun Pan faculty of environmental science and Engineering Kunming University of Science and Technology

17α-Ethynylestradiol（EE2） in natural waters may cause adverse effects on organisms due to its high estrogenic potency. Laboratory studies were performed to study the effects of a local humic acid（LHA）, fulvic acid（LFA） and Aldrich humic acid（AHA） on the photochemical behavior and estrogenic potency of EE2. Here photolytic experiments demonstrated that pure aqueous EE2 could undergo direct and self-sensitized photodegradation at a global rate of 0.0068 hr^-*** rate of EE2 in 5.0 mg/L dissolved humic substances（DHS） was determined to be 0.0274, 0.0296 and 0.0254 hr^-1 for LHA, LFA and AHA, respectively. Reactive oxygen species（ROS） and triplet dissolved humic substances（^3DHS＊） scavenging experiments indicated that the promotion effect of DHS on EE2 photodegradation was mainly aroused by the reactions of HOU（35%–50%）,~1O2（〈10%） andDHS＊（22%–34%）. However, the photodegradation of EE2 could also be inhibited when DHS exceeded the threshold of 10 mg/L. Three hydroxylation products of EE2 were identified using GC–MS and their formation pathways were also proposed. In vitro estrogenicity tests showed that EE2 was transformed into chemicals without estrogenic potency. These findings could extend our knowledge on the photochemical behaviors of steroid estrogens in sunlit natural waters.

关键词： 17α-Ethynylestradiol Photodegradation Dissolved humic substances Reactive oxygen species Estrogenic potency

Metal loaded zeolite adsorbents for hydrogen cyanide removal

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Journal of environmental sciences 2013年第4期25卷 808-814页

作者： Ping Ning Juan Qiu Xueqian Wang Wei Liu Wei Chen faculty of environmental science and Engineering Kunming University of Science and Technology

Metal （Cu, Co, or Zn） loaded ZSM-5 and Y zeolite adsorbents were prepared for the adsorption of hydrogen cyanide （HCN） toxic gas. The results showed that the HCN breakthrough capacity was enhanced significantly when zeolites were loaded with Cu. The physical and chemical properties of the adsorbents that influence the HCN adsorption capacity were analyzed. The maximal HCN breakthrough capacities were about the same for both zeolites at 2.2 mol of HCN/mol of Cu. The Cu2p XPS spectra showed that the possible species present were Cu2O and CuO. The Nls XPS data and FT-IR spectra indicated that CN- would be formed in the presence of Cu＋/Cu2＋ and oxygen gas, and the reaction product could be adsorbed onto Cu/ZSM-5 zeolite more easily than HCN.

关键词： hydrogen cyanide zeolite removal

Effect of zinc and cerium addition on property of copper-based adsorbents for phosphine adsorption

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Journal of Rare Earths 2010年第4期28卷 581-586页

作者：宁平易红宏余琼粉唐晓龙杨丽萍叶智青 faculty of environmental science and Engineering Kunming University of Science & Technology

A series of copper-based activated carbon (AC) adsorbents were prepared in order to investigate the effect of Zn, Ce addition on Cu-based AC adsorbent for phosphine (PH3) adsorption removal from yellow phosphorous tail gas. N2 adsorption isotherm and X-ray diffrac-tion (XRD) results suggested that the addition of Zn could increase the adsorbent ultramicropores, decrease the adsorbent supermicropores and the adsorbent average pore diameter. Therefore it enhanced the PH3 adsorption capacity. Appropriate amoun...

关键词： Cu-based adsorbent zinc cerium phosphine adsorption removal rare earths

Effect of Fe/Cu/Ce loading on the coal-based activated carbons for hydrolysis of carbonyl sulfide

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Journal of Rare Earths 2010年第2期28卷 205-210页

作者：宁平于丽丽易红宏唐晓龙李华王红妍杨丽娜 faculty of environmental science and Engineering Kunming University of Science and Technology

Fe/Cu/Ce modified coal-based activated carbon(AC) was prepared by the sol-gel method,and the effect of Fe/Cu/Ce on catalytic properties of Fe/AC,Fe-Cu/AC and Fe-Cu-Ce/AC was investigated in the hydrolysis of carbonyl sulfide(COS) at 50 °*** surface properties were evaluated by means of nitrogen adsorption and were characterized by using scanning electron microscopy(SEM),X-ray diffracto-metry(XRD) and X-ray photoelectron spectroscopy(XPS).The catalytic activities results showed that addition of Cu and Ce...

关键词： carbonyl sulfide activated carbons metal oxides rare earths

Introduction manner of sulfate acid for improving the performance of SO_4^(2–)/CeO_2 on selective catalytic reduction of NO by NH_3

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Journal of Rare Earths 2016年第7期34卷 667-674页

作者：宋忠贤张秋林宁平刘昕樊洁黄真真 faculty of environmental science and Engineering Kunming University of Science and Technology College of environmental science and Engineering Hunan University

A series of sulfated CeO2 catalysts were synthesized by impregnation and sol-gel methods and used for selective catalytic reduction （SCR） of NOx by NH3. The results showed that the sulfated CeO2 catalysts prepared by sol-gel method showed excellent catalytic activity at 150-50 ℃, and more than 90% NOx conversion was obtained at 232-450 ℃ with a gas hourly space velocity of 60000 h-1. The catalysts were characterized by X-ray diffraction （XRD）, N2 adsorption, Raman, thermogravimetry （TG）, H2-tem- perature-programmed reduction （H2-TPR） and Py-infrared spectroscopy （Py-IR）. The excellent SCR performance was associated with the surface acidity and the micro-structure. The introduction of sulfate acid into CeO2 could increase the amount of BrOnsted and Lewis acid sites over the catalysts, resulting in the improvement of the low temperature activity. The sulfated CeO2 catalysts prepared by sol-gel method possessed lower crystallization degree, excellent redox property and larger specific surface areas, which were responsible for the superior SCR performance.

关键词： sulfated CeO2 selective catalytic reduction surface acidity micro-structure rare earthsO

Activity and hydrothermal stability of CeO_2–ZrO_2–WO_3 for the selective catalytic reduction of NO_x with NH_3

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Journal of environmental sciences 2016年第4期28卷 168-177页

作者： Zhongxian Song Ping Ning Qiulin Zhang Hao Li Jinhui Zhang Yancai Wang Xin Liu Zhenzhen Huang faculty of environmental science and Engineering Kunming University of Science and Technology College of environmental science and Engineering Hunan University

A series of CeO2–ZrO2–WO3（CZW）catalysts prepared by a hydrothermal synthesis method showed excellent catalytic activity for selective catalytic reduction（SCR）of NO with NH3 over a wide temperature of 150–550℃.The effect of hydrothermal treatment of CZW catalysts on SCR activity was investigated in the presence of 10% *** fresh catalyst showed above 90% NOx conversion at 201–459℃,which is applicable to diesel exhaust NOx purification（200–440℃）.The SCR activity results indicated that hydrothermal aging decreased the SCR activity of CZW at low temperatures（below 300℃）,while the activity was notably enhanced at high temperature（above 450℃）.The aged CZW catalyst（hydrothermal aging at 700℃ for 8 hr）showed almost 80% NOx conversion at 229–550℃,while the V2O5–WO3/TiO2 catalyst presented above 80% NOx conversion at 308–370℃.The effect of structural changes,acidity,and redox properties of CZW on the SCR activity was *** results indicated that the excellent hydrothermal stability of CZW was mainly due to the CeO2–ZrO2 solid solution,amorphous WO3 phase and optimal *** addition,the formation of WO3 clusters increased in size as the hydrothermal aging temperature increased,resulting in the collapse of structure,which could further affect the acidity and redox properties.

关键词： CeO2–ZrO2–WO3 Hydrothermal stability Solid solution Acidity

Influence of calcination temperature on selective catalytic reduction of NO_x with NH_3 over CeO_2-ZrO_2-WO_3 catalyst

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Journal of Rare Earths 2015年第7期33卷 726-735页

作者：李军燕宋忠贤宁平张秋林刘昕李昊黄真真 faculty of environmental science and Engineering Kunming University of Science and Technology College of environmental science and Engineering Hunan University

A series of CeO2-ZrO2-WO3 catalysts for the selective catalytic reduction （SCR） of NO with NH3 were prepared by hydrothermal method. The influence of calcination temperature on the catalytic activity, microstructure, surface acidity and redox behavior of CeO2-ZrO2-WO3 catalyst was investigated using various characterization methods. It was found that the CeO2-ZrO2-WO3 catalyst calcined at 600 ℃ showed the best catalytic performance and excellent N2 selectivity, and yielded more than 90% NO conversion in a wide temperature range of 250-500 ℃ with a space velocity （GHSV） of 60000 131. As the calcination temperature was increased from 400 to 600 ℃, the NO conversion obviously increased, but decreased at higher calcination temperature. The results implied that the higher surface area, the strongest synergistic interaction, the superior redox property and the highly dispersed or amorphous WO3 species contributed to the excellent SCR activity of the CeO2-ZrO2-WO3 catalyst calcined at 600℃.

关键词： CeO2-ZrO2-WO3 selective catalytic reduction calcination temperature amorphous synergistic interaction rare earths