期刊文献+
共找到6篇文章
< 1 >
每页显示 20 50 100
Arsenic removal in copper electrolyte:A review and future prospects
1
作者 MA Jun DUAN Ning +2 位作者 XU Fu-yuan JIANG Lin-hua XIAO Ke 《Journal of Central South University》 2025年第5期1736-1759,共24页
Copper is a strategic metal that plays an important role in many industries.In copper metallurgy,electrolytic refining is essential to obtain high-purity copper.However,during the electrolytic refining process,impurit... Copper is a strategic metal that plays an important role in many industries.In copper metallurgy,electrolytic refining is essential to obtain high-purity copper.However,during the electrolytic refining process,impurities such as arsenic are introduced into the electrolyte,which significantly affect the subsequent production and quality of copper products.This paper first discusses the sources,forms,and transformation pathways of arsenic in copper electrolyte during the electrolytic process,then reviews various arsenic removal technologies in detail,including electrowinning,adsorption,solvent extraction,ion exchange,membrane filtration,and precipitation.Particular emphasis is placed on electrowinning,which is the most widely used and mature among these arsenic removal techniques.The paper evaluates these methods based on arsenic removal efficiency,cost effectiveness,technical maturity,environmental friendliness,and operation simplicity.In addition,the paper explores future trends in copper electrolyte purification,focusing on waste reduction at source,resource utilization,intelligent digitalization,and innovations in materials and processes.This review aims to provide researchers and practitioners with a comprehensive and in-depth reference on arsenic removal methods in copper electrolytes. 展开更多
关键词 arsenic removal removal techniques electrolyte purification copper electrorefining ELECTROWINNING
在线阅读 下载PDF
Aerobic biodegradation of di-n-butyl phthalate by Xiangjiang River sediment and microflora analysis 被引量:3
2
作者 周洪波 林峰 +4 位作者 胡培磊 金德才 任洪强 赵晶 邱冠周 《Journal of Central South University》 SCIE EI CAS 2009年第6期948-953,共6页
Di-n-butyl phthalate (DBP),one of phthalate acid esters (PAEs),was investigated to determine its biodegradation rate using Xiangjiang River sediment and find potential DBP degraders in the enrichment culture of the se... Di-n-butyl phthalate (DBP),one of phthalate acid esters (PAEs),was investigated to determine its biodegradation rate using Xiangjiang River sediment and find potential DBP degraders in the enrichment culture of the sediment. The sediment sample was incubated with an initial concentration of DBP of 100 mg/L for 5 d. The biodegradation rate of DBP was detected using HPLC and the degraded products were analyzed by GC/MS. Subsequently,the microbial diversity of the enrichment culture was analyzed by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). The results reveal that almost 100% of DBP is degraded after merely 3 d,generating two main degraded products:mono-butyl phthalate (MBP) and 9-octadecenoic acid. After a six-month enrichment period under the pressure of DBP,the dominant family in the final enrichment culture is clustered with the Comamonas sp.,the remaining are affiliated with Sphingomonas sp.,Hydrogenophaga sp.,Rhizobium sp.,and Acidovorax sp. The results show the potential of these bacteria to be used in the bioremediation of DBP in the environment. 展开更多
关键词 BIOREMEDIATION di-n-butyl phthalate SEDIMENT polymerase chain reaction-restriction fragment length polymorphism microbial diversity
在线阅读 下载PDF
Degradation of chlorothalonil by ultrasonic irradiation:Kinetics and impact factors 被引量:2
3
作者 郭洪光 高乃云 +2 位作者 黎雷 金玄雄 陈喆 《Journal of Central South University》 SCIE EI CAS 2011年第4期1068-1073,共6页
Factors on degradation of chlorothalonil(CLT) in water by high frequency ultrasonic irradiation were investigated.The effects of initial concentration of chlorothalonil,dosages of tertiary butyl alcohol,humic acid and... Factors on degradation of chlorothalonil(CLT) in water by high frequency ultrasonic irradiation were investigated.The effects of initial concentration of chlorothalonil,dosages of tertiary butyl alcohol,humic acid and initial pH value on degradation of chlorothalonil,as well as the reaction mechanism were studied.The results reveal that chlorothalonil could be effectively degradated by ultrasonic irradiation.The reaction constant value kapp decreased from 0.014 1 to 0.010 2 min-1 with the initial concentration increasing from 50 to 400 μg/L during 180 min irradiation.Tertiary butyl alcohol had negative effect on chlorothalonil degradation,while lower concentration of humic acid promoted the sonolysis,and kapp declined with the further concentration increasing.The kapp varied little when the pH value ranged from 3.10 to 10.28.It may be concluded that mechanical and pyrolysis process played main roles on the degradation of chlorothalonil in ultrasonic irradiation rather than ·OH attack.The electrical energy per order(EEo) values for sonolysis degradation of CLT were also calculated to evaluate the cost of the process. 展开更多
关键词 ultrasonic irradiation CHLOROTHALONIL KINETICS impact factors
在线阅读 下载PDF
Removal of lead(II) from aqueous solutions by activated carbon developed from surplus sludge 被引量:1
4
作者 蒋柱武 王学江 宁薛 《Journal of Central South University》 SCIE EI CAS 2014年第9期3568-3574,共7页
Activated carbon(AC) was prepared from surplus sludge using chemical activation method with the assistance of ZnCl2. The influences of process parameters on the AC's specific surface area and adsorption capacity f... Activated carbon(AC) was prepared from surplus sludge using chemical activation method with the assistance of ZnCl2. The influences of process parameters on the AC's specific surface area and adsorption capacity for Pb2+ were examined to optimize these parameters. The optimal conditions for the preparation of AC were determined to be activation temperature of 500 °C, activation time of 1 h, impregnation ratio of 1:1(solid-to-liquid volume) with the 30% ZnCl2 solution(mass fraction), giving the BET surface area of 393.85 m2/g and yield of 30.14% with 33.45% ash. Also, the pyrolysis temperature was found to be the most important parameter in chemical activation. FTIR spectra provided the evidence of some surface structures such as C=C and C—O—C. In the adsorption studies, a rise in solution pH led to a significant increase in adsorption capacity when the pH value varied from 3.0 to 7.0, and the optimal pH for removal of Pb2+ was 7.0. It was observed that the pseudo-second-order equation provided better correlation for the adsorption rate than the pseudo-first-order and the Langmuir model fitted better than the Freundlich model for adsorption isotherm. The adsorption capacity of AC to Pb2+ was 11.75 mg/L at solution pH 7.0, the equilibrium time 480 min and 25 °C. Moreover, the adsorption process is endothermic according to the value of enthalpy change. 展开更多
关键词 sludge-based activated carbon surplus sludge preparation Pb^2+ adsorption
在线阅读 下载PDF
某铅锌冶炼污染场地基于多源信息的重金属稳定化修复及其评价 被引量:1
5
作者 郭小品 李业勋 +6 位作者 左小永 徐业勤 苗进辉 张恒勇 姚佳斌 徐则林 付融冰 《Journal of Central South University》 SCIE EI CAS CSCD 2024年第4期1207-1216,共10页
冶炼污染场地土壤中多重金属复合污染的特征增大了对土壤的修复和最终利用的难度。本研究深入调查了某铅锌冶炼场地土壤重金属污染特征,针对性地制定多种联合稳定化修复方案,采用高精度混合装备添加药剂,实施稳定化修复工程。结果表明,C... 冶炼污染场地土壤中多重金属复合污染的特征增大了对土壤的修复和最终利用的难度。本研究深入调查了某铅锌冶炼场地土壤重金属污染特征,针对性地制定多种联合稳定化修复方案,采用高精度混合装备添加药剂,实施稳定化修复工程。结果表明,Cd、Pb、Zn和As是场地土壤中最主要的重金属污染物,其中Cd、Pb、As的超标率分别为75.80%、76.43%、88.54%。重金属的分布模式与土壤理化性质、污染物迁移路径、水文地质条件、地层岩性、冶炼工艺、厂区功能布局等密切相关。土壤重金属污染主要来源于冶炼粉尘、废渣和废水排放等冶炼活动。稳定化工程效果显示,在药剂与土壤混匀程度不低于90%时,采用无机混合药剂与TJ400螯合剂的组合方案,对土壤稳定化处理7 d后,土壤中Cd、Pb和As同步稳定化效果最好。本研究结果可对多金属重污染场地土壤的稳定化修复提供实践指导。 展开更多
关键词 铅锌冶炼场地 多金属污染土壤 多源信息 稳定化药剂 稳定化工程
在线阅读 下载PDF
冻融及耦合酸化作用下土壤中重金属的浸出性及其机制解析
6
作者 付田雨 李捷 付融冰 《Journal of Central South University》 SCIE EI CAS CSCD 2024年第4期1197-1206,共10页
冻融与不同pH溶液的耦合作用下土壤中重金属浸出行为尚缺乏研究。本研究采用TCLP测试评估了冻融及耦合酸化处理前后土壤中重金属的浸出毒性,并采用孔隙(颗粒)与裂隙图像识别与分析系统(PCAS)和地球化学模拟软件(PHREEQC)分别探究土壤矿... 冻融与不同pH溶液的耦合作用下土壤中重金属浸出行为尚缺乏研究。本研究采用TCLP测试评估了冻融及耦合酸化处理前后土壤中重金属的浸出毒性,并采用孔隙(颗粒)与裂隙图像识别与分析系统(PCAS)和地球化学模拟软件(PHREEQC)分别探究土壤矿物颗粒的微观结构和矿物学演化特征。结果表明,经过30次冻融循环后,As、Cd、Cu、Mn、Pb和Zn的最大浸出浓度分别为0.22 mg/L、0.61 mg/L、2.46 mg/L、3.08 mg/L、29.36 mg/L和8.07 mg/L。在冻融和酸化的耦合作用下,土壤颗粒的孔隙度增加了4.79%。孔隙和裂缝的演化所引起的颗粒结构破坏证实了这一结果。在冻融作用下,土壤颗粒的各向异性增加,而在冻融与酸化的耦合作用下,土壤颗粒的各向异性降低。SEM-EDS、PCAS量化和PHREEQC模拟的结果表明,重金属的释放机制不仅与矿物颗粒的微观结构演化特征有关,还受质子腐蚀以及矿物的溶解和沉淀的影响。这些结果将为季节性冻土地区污染场地土壤修复评价提供重要参考。 展开更多
关键词 污染土壤 重金属浸出性 冻融循环 酸化 孔隙(颗粒)与裂隙图像识别与分析系统(PCAS) PHREEQC软件
在线阅读 下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部