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首页> 外文期刊>International Journal of Electrochemical Science >Synthesis and Characterization of Uncracked IrO2?SnO2?Sb2O3?Oxide Films Using Organic Precursors and Their Application for the Oxidation of Tartrazine and Dibenzothiophene
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Synthesis and Characterization of Uncracked IrO2?SnO2?Sb2O3?Oxide Films Using Organic Precursors and Their Application for the Oxidation of Tartrazine and Dibenzothiophene

机译:使用有机前体的未粘接的IRO2?SB2O3氧化物膜的合成和表征及其用于氧化塔拉嗪和二苯并噻吩的氧化

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A ternary coating film of IrO2?SnO2?Sb2O3 on a Ti substrate was prepared by thermal decomposition in an adapted protocol of the Pechini method to obtain DSA type electrodes. The polymeric precursor mixture was prepared with nonchlorinated salts of iridium, tin, and antimony in different molar proportions. Iridium(III) acetylacetonate, tin(II) acetate, and antimony(III) acetate were used in small amounts to obtain compact, thin, and uncracked oxide films with homogeneous texture compared with a commercial film of Ti|IrO2?SnO2?Sb2O5. The polymeric precursor solution was brushed onto a pretreated titanium substrate and calcined at 500 °C to convert the coating into IrO2?SnO2?Sb2O3. Physical and electrochemical characterization was performed by SEM, EDX, DRX, and cyclic voltammetry. The formation of ternary oxides was explained according to redox reaction mechanisms involving decarboxylation and thermal decomposition. Even though the polymeric precursor solution was deposited by brushing, the oxide films was thin and homogeneous (3.05 ± 0.35 μm thickness). The DSA electrode performance was tested to evaluate the electrochemical oxidation of tartrazine and dibenzothiophene in aqueous and acetonitrile/water media, respectively. All DSAs demonstrated high effectiveness for the decolorization and mineralization of tartrazine (up to 90% and 70%, respectively), mainly by hydroxyl radicals. On the other hand, dibenzothiophene was converted to both dibenzothiophene sulfoxide and dibenzothiophene sulfone by direct electron transfer.
机译:通过在Pechini方法的适应方案中,通过热分解制备Ti衬底上的IRO2αSB2O3的三元涂膜,以获得DSA型电极。将聚合物前体混合物用铱,锡和锑的非氯化盐制备,以不同的摩尔比例制备。铱(III)乙酰丙酮,乙酸锡和乙酸锡和锑(III)乙酸盐以少量使用,与Ti 2的商业膜相比,少量获得具有均匀质地的紧凑,薄的和未包克的氧化膜。将聚合物前体溶液刷涂到预处理的钛基底上并在500℃下煅烧以将涂层转化为IRO2?SB2O3。通过SEM,EDX,DRX和循环伏安法进行物理和电化学表征。根据涉及脱羧和热分解的氧化还原反应机制来解释三元氧化物的形成。即使通过刷涂沉积聚合物前体溶液,氧化膜也薄且均匀(3.05±0.35μm厚)。测试DSA电极性能以分别评价塔拉嗪和二苯并噻吩在水性和乙腈/水介质中的电化学氧化。所有DSA均对塔拉嗪的脱色和矿化(分别高达90%和70%),主要是羟基自由基的高效果。另一方面,通过直接电子转移将二苯并噻吩转化为二苯并噻吩硫氧化物和二苯并噻吩砜。

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