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华 中 农 业 大 学 学 报 第 39 卷
环境污染物降解过程中的作用机制还需要进一步的 [ 8 ] ZENGL , MCKINLEYJW.De g radationof p entachloro p henol
完善.对于此项研究工作, 我们认为还有以下几个 ina q ueoussolution b y audibleGfre q uenc y sonol y tic ozonation
[ J ] .Journalofhazardousmaterials , 2006 , 135 : 218G225
方面需要解决:
[ 9 ] DINGX , WANG S , SHEN W , etal.Fe@Fe 2O 3p romotedelectroG
1 ) 活性氧物种产生方法的优化.当前活性氧物
chemicalmineralizationofatrazineviaatriazinonrin go p enin g
种产生方法众多, 但是容易受二次污染、 效率低、 工 mechanism [ J ] .Waterresearch , 2017 , 112 : 9G18.
序复杂等条件限制, 因此, 开发绿色、 高效、 便捷的活 [ 10 ] HUANGX , HOU X , JIAF , etal.AscorbateG p romotedsurface
性氧物种产生新方法十分重要. ironc y cleforefficienthetero g eneousFentonalachlorde g radaG
2 ) 活性氧物种的定量检测.活性氧物种作为一 tionwithhematitenanocr y stals [ J ] .ACSa pp liedmaterials&
interfaces , 2017 , 9 ( 10 ): 8751G8758.
类反应活性高的中间体, 极易在自然环境条件下猝
[ 11 ] NOSAKA Y , NOSAKA A Y.GenerationanddetectionofreacG
灭, 其寿命十分短暂.在反应过程中捕获和检测这
tiveox yg ens p eciesinp hotocatal y sis [ J ] .Chemicalreviews ,
些含量极少的活性氧物种往往十分困难, 对其进行 2017 , 117 ( 17 ): 11302G11336.
准确的定量检测也十分困难.这需要我们研究开发 [ 12 ] FENTON HJH , JACKSON HJ.Oxidationof p ol y h y dricalcoG
holsinp resenceofiron [ J ] .Journalofthechemicalsociet y ,
出更灵敏的活性氧物种检测手段.
3 ) 多种活性氧物种协同降解机制的研究.在高 transactions , 1894 , 65 : 899G910.
[ 13 ] LI H , SHANGJ , YANG Z , etal.Ox yg envacanc yassociated
级氧化技术去除污染物过程中, 其中活性氧物种的
surfaceFentonchemistr y : surfacestructurede p endenth y droxG
生成过程相对比较复杂, 活性氧物种的产生往往不 y lradicalsg enerationandsubstratede p endentreactivit y [ J ] .
是单一的, 而是多种活性氧物种同时产生, 活性氧物 Environmentalscience & technolo gy , 2017 , 51 ( 10 ): 5685G
种中间也发生了相互转化.因此, 在研究活性氧物 5694.
种降解作用机制时, 仅考虑一种活性氧物种是不全 [ 14 ] MU Y , AIZ , ZHANG L.Phos p hateshiftedox yg enreduction
p athwa yonFe@Fe 2O 3coreGshellnanowiresforenhancedreG
面的.研究多种活性氧物种协同降解机制更能模拟
activeox yg ens p eciesg enerationandaerobic4Gchloro p henol
实际污染物处理过程.
de g radation [ J ] .Environmentalscience&technolo gy , 2017 , 51
( 14 ): 8101G8109.
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