应用化工
應用化工
응용화공
APPLIED CHEMICAL INDUSTRY
2014年
10期
1930-1934
,共5页
曾飞虎%张青海%林继辉%林秋容
曾飛虎%張青海%林繼輝%林鞦容
증비호%장청해%림계휘%림추용
碱性品红%羟基氧化铁%过氧化氢%羟基自由基%零电荷点
堿性品紅%羥基氧化鐵%過氧化氫%羥基自由基%零電荷點
감성품홍%간기양화철%과양화경%간기자유기%령전하점
fuehsin%FeOOH%H2 O2%hydroxyl radieals%point of zero eharge
采用FeOOH/H2 O2体系对一种碱性阳离子染料进行催化降解。考察了H2 O2浓度、FeOOH的投加量、碱性品红的浓度、pH对碱性品红降解的影响。结果表明,反应的较优条件是H2 O2浓度为60 mmol/L,FeOOH投加量1.0 g/L;碱性品红浓度高的降解速率比较慢,浓度低的降解速率快;pH=1时,碱性品红去除率为90.9%;pH=9时,碱性品红去除率为98.9%。机理研究表明,当溶液pH小于FeOOH的零电荷点时,FeOOH表面带正电荷,与带正电荷的碱性品红之间相互排斥降低了对碱性品红的吸附作用,同时部分 Fe离子发生溶解,溶解的铁离子与H2 O2形成Fenton 体系;当溶液 pH 大于 FeOOH 的零电荷点时,FeOOH 带负电荷,碱性品红因静电力被吸附在FeOOH表面,同时与产生的羟基自由基发生反应。
採用FeOOH/H2 O2體繫對一種堿性暘離子染料進行催化降解。攷察瞭H2 O2濃度、FeOOH的投加量、堿性品紅的濃度、pH對堿性品紅降解的影響。結果錶明,反應的較優條件是H2 O2濃度為60 mmol/L,FeOOH投加量1.0 g/L;堿性品紅濃度高的降解速率比較慢,濃度低的降解速率快;pH=1時,堿性品紅去除率為90.9%;pH=9時,堿性品紅去除率為98.9%。機理研究錶明,噹溶液pH小于FeOOH的零電荷點時,FeOOH錶麵帶正電荷,與帶正電荷的堿性品紅之間相互排斥降低瞭對堿性品紅的吸附作用,同時部分 Fe離子髮生溶解,溶解的鐵離子與H2 O2形成Fenton 體繫;噹溶液 pH 大于 FeOOH 的零電荷點時,FeOOH 帶負電荷,堿性品紅因靜電力被吸附在FeOOH錶麵,同時與產生的羥基自由基髮生反應。
채용FeOOH/H2 O2체계대일충감성양리자염료진행최화강해。고찰료H2 O2농도、FeOOH적투가량、감성품홍적농도、pH대감성품홍강해적영향。결과표명,반응적교우조건시H2 O2농도위60 mmol/L,FeOOH투가량1.0 g/L;감성품홍농도고적강해속솔비교만,농도저적강해속솔쾌;pH=1시,감성품홍거제솔위90.9%;pH=9시,감성품홍거제솔위98.9%。궤리연구표명,당용액pH소우FeOOH적령전하점시,FeOOH표면대정전하,여대정전하적감성품홍지간상호배척강저료대감성품홍적흡부작용,동시부분 Fe리자발생용해,용해적철리자여H2 O2형성Fenton 체계;당용액 pH 대우 FeOOH 적령전하점시,FeOOH 대부전하,감성품홍인정전력피흡부재FeOOH표면,동시여산생적간기자유기발생반응。
The eatalytie degradation of fuehsin using FeOOH/H2 O2 system was investigated. The effeets of H2 O2 eoneentration,FeOOH dosage,fuehsin eoneentration and pH on fuehsin degradation were diseussed in detail. The results showed that the optimum eonditions were as follows:H2 O2 eoneentration 60 mmol/L and FeOOH dosage 1. 0 g/L;The degradation rate of fuehsin in high eoneentration was slow,on the eon-trary,that in low eoneentration was fast;The removal rate of fuehsin was 90. 9% at pH=1,but whieh was 98 . 9% at pH=9;The meehanistie studies suggested that absorption of fuehsin was redueed due to the re-pulsion between positively eharge of fuehsin and positively eharged surfaee of FeOOH eaused when the so-lution pH was less than the point of zero eharge of FeOOH. Meanwhile,part of ferrie ions dissolved then Fenton system was formed by H2 O2 and dissolved ferrie ion;On the eontrary,when the solution pH was more than the point of zero eharge of FeOOH,the fuehsin was absorbed on the surfaee of negatively eharge surfaee of FeOOH by eleetrostatie foree and reaeted with produeed hydroxyl radieals.