检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:魏健[1,2] 邓雪娇[1,3] 宋永会[1,2] 肖书虎[1] 徐东耀[3]
机构地区:[1]中国环境科学研究院城市水环境研究科技创新基地,北京100012 [2]北京师范大学水科学研究院,北京100875 [3]中国矿业大学(北京)化学与环境工程学院,北京100083
出 处:《环境工程学报》2013年第7期2529-2535,共7页Chinese Journal of Environmental Engineering
基 金:国家"水体污染控制与治理"科技重大专项(2012ZX07202002);中法国际合作项目(2010DFB90590-03);国家自然科学基金资助项目(21107103)
摘 要:以Ti金属网为阴极,Ti基RuO2涂层形稳电极为阳极,采用外加H2O2和Fe2+的方式,研究了电-Fenton氧化预处理干法腈纶生产废水的工艺,考察了H2O2投加量、Fe2+投加量、pH值和电流强度等因素对污染物降解过程的影响,分析了废水可生化性和污染物变化规律。结果表明,电-Fenton法可以有效降解废水中有机污染物,使废水COD迅速降低,在初始pH值为3.0,Fe2+投加量为5.0 mmol/L,H2O2投加量为60.0 mmol/L,电流强度0.2 A的条件下,反应120 min后COD去除率可以达到44.0%以上;反应过程中H2O2的投加方式对电-Fenton法的处理效果具有明显影响,H2O2分6次投加可以使COD去除率由一次性投加时的44.8%提高至54.1%;处理后废水的BOD5/COD由0.29升高至0.68;GC-MS结果表明,经电-Fenton法预处理后,废水中多数芳香族化合物和特征污染物能被有效降解。An electro-Fenton oxidation process using Ti sheet as cathode and RuO2/Ti as anode was established for the pretreatment of dry-spun acrylic fiber manufacturing wastewater. The effects of initial pH value, c(H2O2), c(Fe2+) and current intensity on the removals of organic pollutants were investigated. The variations of biodegradability and organic pollutants were also analyzed. The results showed that the organic pollutants were degraded efficiently and the COD removal efficiency reached above 44.0% under the optimized conditions with initial pH value of 3.0, c(H2O2) of 60.0 mmol/L, c(Fe2+) of 5.0 mmol/L and current intensity of 0.2 A. The feeding mode of H2O2 had significant influence on COD removal efficiency: the removal efficiency was 44.8% if all the H2O2 were fed in one time, while it would reach 54.1% if the total H2O2 was divided into 6 portions and fed by 6 times. The BOD5/COD ratio increased from 0.29 to 0.68 after 240 min treatment. GC-MS analysis showed that most of the aromatic and other typical organics were degraded in the electro-Fenton process.
关 键 词:腈纶废水 电-FENTON 可生化性 GC—MS
分 类 号:X703[环境科学与工程—环境工程]
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.14