Catalytic degradation of Acid Orange 7 by H2O2 as promoted by either bare or V-loaded titania under UV light, in dark conditions, and after incubating the catalysts in ascorbic acid

Q1 Materials Science Catalysis Structure & Reactivity Pub Date : 2015-10-02 DOI:10.1080/2055074X.2015.1105618
M. Piumetti, F. Freyria, M. Armandi, G. Saracco, E. Garrone, G. Gonzalez, B. Bonelli
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引用次数: 12

Abstract

Abstract Pure and V-loaded mesoporous titania (with 2.5 wt-% V) were prepared by template-assisted synthesis and compared to commercial titania (Degussa P25), both as such and after vanadium loading. Mesoporous TiO2 occurred as pure anatase nanoparticles with higher surface area (SSA = 150 m2 g−1) than P25 (SSA = 56 m2 g−1). Degradation of the azo dye Acid Orange 7 by H2O2 was used as a test reaction: under UV light, no difference emerged between mesoporous TiO2 and P25, whereas in dark conditions, higher SSA of the mesoporous sample resulted in higher conversions. Under UV illumination, surface V5+ species inhibited photocatalytic activity, by forming inactive V4+ species. Similarly, in dark conditions, V5+ surface species reacted with H2O2, likely yielding ·O2H radicals and reducing to V4+. On the contrary, V-containing catalysts were very active after pretreatment with ascorbic acid, which reduced V5+ species to V3+species, the latter promoting very lively a Fenton-like reaction.
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在紫外光、黑暗条件和抗坏血酸培养条件下,裸钛和载v钛对H2O2催化降解酸橙7的影响
通过模板辅助合成制备了纯V负载介孔二氧化钛(2.5 wt-% V),并与市售二氧化钛(Degussa P25)进行了比较。介孔TiO2以纯锐钛矿纳米颗粒形式出现,其表面积(SSA = 150 m2 g−1)高于P25 (SSA = 56 m2 g−1)。用H2O2降解偶氮染料酸橙7作为测试反应:在紫外光下,介孔TiO2和P25没有差异,而在黑暗条件下,介孔样品的SSA越高,转化率越高。在紫外光照射下,表面V5+通过形成无活性的V4+抑制光催化活性。同样,在黑暗条件下,V5+表面物质与H2O2反应,可能产生·O2H自由基并还原为V4+。相反,含v催化剂经抗坏血酸预处理后具有很强的活性,将V5+还原为V3+, V3+促进了非常活跃的Fenton-like反应。
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来源期刊
Catalysis Structure & Reactivity
Catalysis Structure & Reactivity CHEMISTRY, PHYSICAL-
CiteScore
4.80
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