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Electrochemical oxidation of represe...
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Kim, Jaeshin.
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Electrochemical oxidation of representative inorganic and organic contaminants in an in situ electrochemical reactor.
紀錄類型:
書目-語言資料,印刷品 : Monograph/item
正題名/作者:
Electrochemical oxidation of representative inorganic and organic contaminants in an in situ electrochemical reactor./
作者:
Kim, Jaeshin.
面頁冊數:
179 p.
附註:
Adviser: Gregory V. Korshin.
Contained By:
Dissertation Abstracts International67-02B.
標題:
Engineering, Environmental. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3207819
ISBN:
9780542560293
Electrochemical oxidation of representative inorganic and organic contaminants in an in situ electrochemical reactor.
Kim, Jaeshin.
Electrochemical oxidation of representative inorganic and organic contaminants in an in situ electrochemical reactor.
- 179 p.
Adviser: Gregory V. Korshin.
Thesis (Ph.D.)--University of Washington, 2006.
The results of this research considerably improve the understanding of the mechanisms that govern the EC generation of reactive species and in situ environmental oxidations in EC reactors.
ISBN: 9780542560293Subjects--Topical Terms:
783782
Engineering, Environmental.
Electrochemical oxidation of representative inorganic and organic contaminants in an in situ electrochemical reactor.
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This study was focused on the investigation of indirect electrochemical (EC) oxidation of selected environmentally important species (arsenite, phenol, nonylphenol and natural organic matter (NOM)) in an EC reactor equipped with a Co-PbO2 anode and a stainless steel cathode. The EC production of hydroxyl radicals was determined to be of fundamental importance for in situ EC oxidations. Ozone in such systems is apparently formed a result of interactions between EC-generated OH· radicals and molecular oxygen rather than via direct EC oxidation of water to O3. O 3 and OH· formation was quantified using indigotrisulfonate and p-chlorobenzoic acid (pCBA). The current yield of hydroxyl radicals (alpha OH·) increased from 0.1 to 0.5% as the current density was increased from 5 to 50 mA/cm2. The value of alpha OH· was not affected by variations of pH (range 5 to 9) and/or total carbonate concentration (range 0 to 2 mM). In addition to OH· and O3, free chlorine was generated by EC oxidation of chloride ion. The yield of EC-generated chlorine was strongly correlated with the Cl- concentration.
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The pathways and kinetics of the EC oxidation of arsenite and phenolic compounds were examined. Arsenite was oxidized by several EC-produced oxidants, but phenol and nonylphenol were oxidized almost exclusively by hydroxyl radicals. The consumption of OH· radicals in the oxidation of the phenols caused the yields of ozone to decrease, due to the suppression of reactions between OR and dissolved oxygen. The EC oxidation of phenol and nonylphenol was partially reversible due to the formation of benzoquinone intermediates that could be reduced by cathodically generated species. The formation of such intermediates was not discernible for NOM. The EC oxidation of NOM was accompanied by the breakdown of the aromatic structures in NOM molecules and formation of low molecular weight aldehydes and carboxylic acids whose speciation was similar to that seen in the oxidation of nonylphenol.
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