摘要
以偶氮染料橙黄G(OG)为目标污染物,研究Fe2+分别催化H2O2、S2O82-、H2O2-S2O82-降解0.1 mmol/LOG Fe2+/H2O2体系,[Fe2+]=1 mmol/L,pH=3,[H2O2]0=10 mmol/L,降解30 min OG脱色率为96%,随着pH值增大和[H2O2]0>10 mmol/L,OG脱色率减小,呈线性变化。Fe2+/S2O82-体系,随着S2O82-初始浓度增加OG脱色率增大,随着pH值增大OG脱色率减小,呈非线性变化。Fe2+/H2O2-S2O82-体系,pH=3,[H2O2]0=2 mmol/L,[S2O82-]0>10 mmol/L时OG脱色率持续增大。Fe2+/H2O2-S2O82-体系矿化率最高。利用乙醇和硝基苯作为分子探针,采用分子探针竞争实验鉴定该体系中产生的SO4.和OH.。
The oxidative degradation of 0.1 mmol/L orange G（OG） in Fe2＋/H2O2、Fe2＋/S2O82-、 Fe2＋/H2O2-S2O82-was studied.In the Fe2＋/H2O2 reaction,under the optimum condition（pH=3,[H2O2]0=10 mmol/L and [Fe2＋]0=1 mmol/L）,OG degradation in aqueous solutions with initial concentration of 0.1 mmol/L reached 96% within 30 min.However,retardation was observed if H2O2 was overdosed.Such retardation was not observed in the Fe2＋/S2O82-system,but a nonlinear increment of removal efficiency was identified.Degradation of OG was enhanced with increasing S2O82-initial concentration but decreased at the presence of hydroxyl ion.In the aqueous system of initial pH value of 3,the optimal operation condition of Fe2＋/H2O2-S2O82-was determined to be H2O2concentration 2 mmol/L.OG degradation increased with increasing dosage of persulfate.Furthermore,it was experimentally found that the Fe2＋/H2O2-S2O82-process on the other hand showed the best mineralization in OG degradation.The sulfate free radical and hydroxyl free radical produced in the system were determined by molecular probes（ethanol and nitrobenzene） methods,and the reaction mechanism of producing sulfate free radical in the Fe2＋/H2O2-S2O82-system was discussed.
出处
《化工进展》
EI
CAS
CSCD
北大核心
2012年第10期2330-2334,共5页
Chemical Industry and Engineering Progress
基金
广东省首批"节能减排"重大专项(2008A080800003)
关键词
硫酸根自由基
橙黄G
过硫酸钠
过氧化氢
sulfate radical
orange G
sodium persulfate
hydrogen peroxide
