Accelerating the(NH_4)_(2)SO_(3) oxidation gives rise to the reclaiming of byproduct, while there are secondary environmental risks from reduction of the coexisted selenium species by sulfite. In this study, a bi-func...Accelerating the(NH_4)_(2)SO_(3) oxidation gives rise to the reclaiming of byproduct, while there are secondary environmental risks from reduction of the coexisted selenium species by sulfite. In this study, a bi-functional Co-SBA-15-SH, were synthesized through Co impregnation and sulfhydryl(-SH) decoration, which can simultaneously uptake Se and accelerate sulfite oxidation efficiently. Meanwhile, the adsorption kinetics and migration mechanism of Se species were revealed through characterization and density functional calculations, with maximum adsorption capacity of 223 mg/g. The inhibition of Se~0 re-emission and poisonous effect of Se on sulfite oxidation was also investigated. Using the findings of this study, the ammonia desulfurization can be improved by enabling purification of the byproduct and lowering the toxicity of effluent by removing toxic pollutants.展开更多
The toxic cyanides in cyanide residues produced from cyanidation process for gold extraction are harmful to the environment.Pyrite is one of the main minerals existing in cyanide residues.In this work,the interaction ...The toxic cyanides in cyanide residues produced from cyanidation process for gold extraction are harmful to the environment.Pyrite is one of the main minerals existing in cyanide residues.In this work,the interaction of cyanide with pyrite and the decyanation of pyrite cyanide residue were analyzed.Results revealed that high pH value,high cyanide concentration,and high pyrite dosage promoted the interaction of cyanide with pyrite.The cyanidation of pyrite was pseudo-second-order with respect to cyanide.The decyanation of pyrite cyanide residue by Na_(2)SO_(3)/air oxidation was performed.The cyanide removal efficiency was 83.9% after 1 h of reaction time under the optimal conditions of pH value of 11.2,SO_(3)^(2-) dosage of 22 mg·g^(-1),and air flow rate of 1.46 L·min^(-1).X-ray photoelectron spectroscopy analysis of the pyrite samples showed the formation of Fe(Ⅲ)and FeSO_(4) during the cyanidation process.The cyanide that adsorbed on the pyrite surface after cyanidation mainly existed in the forms of free cyanide(CN^(-))and ferrocyanide(Fe(CN)_(6)^(4-)),which were effectively removed by Na_(2)SO_(3)/air oxidation.During the decyanation process,air intake promoted pyrite oxidation and weakened cyanide adsorption on the pyrite surface.This study has practical significance for gold enterprises aiming to mitigate the environmental impact related to cyanide residues.展开更多
Oxidation of S（IV） to S（VI） in the effluent of a flue gas desulfurization（FGD） sys- tem is very critical for industrial applications of seawater FGD. This paper reports a pulsed corona discharge oxidation proces...Oxidation of S（IV） to S（VI） in the effluent of a flue gas desulfurization（FGD） sys- tem is very critical for industrial applications of seawater FGD. This paper reports a pulsed corona discharge oxidation process combined with a TiO2 photocatalyst to convert S（IV） to S（VI） in artificial seawater. Experimental results show that the oxidation of S（IV） in artificial seawater is enhanced in the pulsed discharge plasma process through the application of TiO2 coating electrodes. The oxidation rate of S（IV） using Ti metal as a ground electrode is about 2.0x10-4 mol. L 1. min-1, the oxidation rate using TiO2/Ti electrode prepared by annealing at 500 ~C in air is 4.5x 10-4 tool. L-a ~ min-1, an increase with a factor 2.25. The annealing temper- ature for preparing TiO2/Ti electrode has a strong effect on the oxidation of S（IV） in artificial seawater. The results of in-situ emission spectroscopic analysis show that chemically active species （i.e. hydroxyl radicals and oxygen radicals） are produced in the pulsed discharge plasma process. Compared with the traditional air oxidation process and the sole plasma-induced oxidation process, the combined application of TiO2 photocatalysts and a pulsed high-voltage electrical discharge process is useful in enhancing the energy and conversion efficiency of S（IV） for the seawater FGD system.展开更多
A pore-array intensified tube-in-tube microchannel(PA-TMC),which is characterized by high throughput and low pressure drop,was developed as a gas–liquid contactor.The sulfite oxidation method was used to determine th...A pore-array intensified tube-in-tube microchannel(PA-TMC),which is characterized by high throughput and low pressure drop,was developed as a gas–liquid contactor.The sulfite oxidation method was used to determine the oxygen efficiency(φ)and volumetric mass transfer coefficient(k_(L)a)of PA-TMC,and the mass transfer amount per unit energy(ε)was calculated by using the pressure drop.The effects of structural and operating parameters were investigated systematically,and the twophase flow behavior was monitored by using a charge-coupled device imaging system.The results indicated that the gas absorption efficiency and mass transfer performance of the PA-TMC were improved with increasing pore number,flow rate,and number of helical coil turns and decreasing pore size,row number,annular size,annular length,and surface tension.Theφ,εand k La of PA-TMC could reach 31.3%,1.73×10^(-4) mol/J,and 7.0 s-1,respectively.The Sherwood number was correlated with the investigated parameters to guide the design of PA-TMC in gas absorption and mass transfer processes.展开更多
We report the synthesis of ordered mesoporous ceria(mCeO_(2))with highly crystallinity and thermal stability using hybrid polymer templates consisting of organosilanes.Those organosilane-containing polymers can conver...We report the synthesis of ordered mesoporous ceria(mCeO_(2))with highly crystallinity and thermal stability using hybrid polymer templates consisting of organosilanes.Those organosilane-containing polymers can convert into silica-like nanostructures that further serve as thermally stable and mechanically strong templates to prevent the collapse of mesoporous frameworks during thermal-induced crystallization.Using a simple evaporation-induced self-assembly process,control of the interaction between templates and metal precursors allows the co-self-assembly of polymer micelles and Ce^(3+)ions to form uniform porous structures.The porosity is well-retained after calcination up to 900℃.After the thermal engineering at 700℃ for 12 h(mCeO_(2)-700-12 h),mCeO_(2) still has a specific surface area of 96 m^(2) g^(−1) with a pore size of 14 nm.mCeO_(2) is demonstrated to be active for electrochemical oxidation of sulfite.mCeO_(2)-700-12 h with a perfect balance of crystallinity and porosity shows the fastest intrinsic activity that is about 84 times more active than bulk CeO_(2) and 5 times more active than mCeO_(2) that has a lower crystallinity.展开更多
文摘Accelerating the(NH_4)_(2)SO_(3) oxidation gives rise to the reclaiming of byproduct, while there are secondary environmental risks from reduction of the coexisted selenium species by sulfite. In this study, a bi-functional Co-SBA-15-SH, were synthesized through Co impregnation and sulfhydryl(-SH) decoration, which can simultaneously uptake Se and accelerate sulfite oxidation efficiently. Meanwhile, the adsorption kinetics and migration mechanism of Se species were revealed through characterization and density functional calculations, with maximum adsorption capacity of 223 mg/g. The inhibition of Se~0 re-emission and poisonous effect of Se on sulfite oxidation was also investigated. Using the findings of this study, the ammonia desulfurization can be improved by enabling purification of the byproduct and lowering the toxicity of effluent by removing toxic pollutants.
基金financially supported by the National Natural Science Foundation of China(No.52274348)the Major projects for the“Revealed Top”Science and Technology of Liaoning Province,China(No.2022JH1/10400024)the National Key Research and Development Program of China(No.2018YFC1902002).
文摘The toxic cyanides in cyanide residues produced from cyanidation process for gold extraction are harmful to the environment.Pyrite is one of the main minerals existing in cyanide residues.In this work,the interaction of cyanide with pyrite and the decyanation of pyrite cyanide residue were analyzed.Results revealed that high pH value,high cyanide concentration,and high pyrite dosage promoted the interaction of cyanide with pyrite.The cyanidation of pyrite was pseudo-second-order with respect to cyanide.The decyanation of pyrite cyanide residue by Na_(2)SO_(3)/air oxidation was performed.The cyanide removal efficiency was 83.9% after 1 h of reaction time under the optimal conditions of pH value of 11.2,SO_(3)^(2-) dosage of 22 mg·g^(-1),and air flow rate of 1.46 L·min^(-1).X-ray photoelectron spectroscopy analysis of the pyrite samples showed the formation of Fe(Ⅲ)and FeSO_(4) during the cyanidation process.The cyanide that adsorbed on the pyrite surface after cyanidation mainly existed in the forms of free cyanide(CN^(-))and ferrocyanide(Fe(CN)_(6)^(4-)),which were effectively removed by Na_(2)SO_(3)/air oxidation.During the decyanation process,air intake promoted pyrite oxidation and weakened cyanide adsorption on the pyrite surface.This study has practical significance for gold enterprises aiming to mitigate the environmental impact related to cyanide residues.
基金supported by National Natural Science Foundation of China(Nos.20836008,21076188,20976158 and 21076189)the National Key Technology Research and Development Program of the Ministry of Science and Technology of China(No.2008BAC32B06)the Zhejiang Provincial Natural Science Foundation of China(No.LY12B07001)
文摘Oxidation of S（IV） to S（VI） in the effluent of a flue gas desulfurization（FGD） sys- tem is very critical for industrial applications of seawater FGD. This paper reports a pulsed corona discharge oxidation process combined with a TiO2 photocatalyst to convert S（IV） to S（VI） in artificial seawater. Experimental results show that the oxidation of S（IV） in artificial seawater is enhanced in the pulsed discharge plasma process through the application of TiO2 coating electrodes. The oxidation rate of S（IV） using Ti metal as a ground electrode is about 2.0x10-4 mol. L 1. min-1, the oxidation rate using TiO2/Ti electrode prepared by annealing at 500 ~C in air is 4.5x 10-4 tool. L-a ~ min-1, an increase with a factor 2.25. The annealing temper- ature for preparing TiO2/Ti electrode has a strong effect on the oxidation of S（IV） in artificial seawater. The results of in-situ emission spectroscopic analysis show that chemically active species （i.e. hydroxyl radicals and oxygen radicals） are produced in the pulsed discharge plasma process. Compared with the traditional air oxidation process and the sole plasma-induced oxidation process, the combined application of TiO2 photocatalysts and a pulsed high-voltage electrical discharge process is useful in enhancing the energy and conversion efficiency of S（IV） for the seawater FGD system.
基金supported by National Key Research and Development Program(No.2016YFD0501402-04)National Natural Science Foundation of China(Nos.21776179,21621004)the Program for Changjiang Scholars and Innovative Research Team in University(No.IRT_15R46)。
文摘A pore-array intensified tube-in-tube microchannel(PA-TMC),which is characterized by high throughput and low pressure drop,was developed as a gas–liquid contactor.The sulfite oxidation method was used to determine the oxygen efficiency(φ)and volumetric mass transfer coefficient(k_(L)a)of PA-TMC,and the mass transfer amount per unit energy(ε)was calculated by using the pressure drop.The effects of structural and operating parameters were investigated systematically,and the twophase flow behavior was monitored by using a charge-coupled device imaging system.The results indicated that the gas absorption efficiency and mass transfer performance of the PA-TMC were improved with increasing pore number,flow rate,and number of helical coil turns and decreasing pore size,row number,annular size,annular length,and surface tension.Theφ,εand k La of PA-TMC could reach 31.3%,1.73×10^(-4) mol/J,and 7.0 s-1,respectively.The Sherwood number was correlated with the investigated parameters to guide the design of PA-TMC in gas absorption and mass transfer processes.
基金J H is grateful for the financial support from National Science Foundation(CEBT-1705566)The HR-TEM studies were performed using the facilities in the UConn Thermo Fisher Scientific Center for Advanced Microscopy and Materials Analysis(CAMMA).Low-magnification TEM and SEM images were obtained at the Biosciences Electron Microscopy Facility at the University of ConnecticutThis work was also partially supported by the Green Emulsions Micelles and Surfactants(GEMS)Center of the University of Connecticut.
文摘We report the synthesis of ordered mesoporous ceria(mCeO_(2))with highly crystallinity and thermal stability using hybrid polymer templates consisting of organosilanes.Those organosilane-containing polymers can convert into silica-like nanostructures that further serve as thermally stable and mechanically strong templates to prevent the collapse of mesoporous frameworks during thermal-induced crystallization.Using a simple evaporation-induced self-assembly process,control of the interaction between templates and metal precursors allows the co-self-assembly of polymer micelles and Ce^(3+)ions to form uniform porous structures.The porosity is well-retained after calcination up to 900℃.After the thermal engineering at 700℃ for 12 h(mCeO_(2)-700-12 h),mCeO_(2) still has a specific surface area of 96 m^(2) g^(−1) with a pore size of 14 nm.mCeO_(2) is demonstrated to be active for electrochemical oxidation of sulfite.mCeO_(2)-700-12 h with a perfect balance of crystallinity and porosity shows the fastest intrinsic activity that is about 84 times more active than bulk CeO_(2) and 5 times more active than mCeO_(2) that has a lower crystallinity.
