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Boreskov Institute of Catalysis of the Siberian Branch of Russian ...

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PP-IV-31PHOTOCATALYTICAL ACTIVITY OF HEAT-RESISTANTTITANIUM DIOXIDE ALLOYED WITH ANION IMPURITIESSedneva T.A., Lokshin E.P., Kalinnikov V.T.<strong>Institute</strong> <strong>of</strong> Chemistry and Technology <strong>of</strong> Rare Elements and Mineral Raw Materials RAS(Kola Science Centre), Apatity, Murmansk Regione-mail: sedneva@chemy.kolasc.net.ruIt is known that photocatalytical systems on <strong>the</strong> basis <strong>of</strong> TiO 2 are capable, when exposedto UV radiation, <strong>of</strong> providing an environmentally friendly, reagentless decomposition <strong>of</strong>organic and bacterial contamination <strong>of</strong> air in flow-type reactors. For effluent purification,especially in regions with fairly intense daylight illumination, more promising areaccumulation tanks with periodically regenerated photocatalyst [1-3].The conventional photocatalyst applied worldwide is TiO 2 <strong>of</strong> P25 brand produced byDegussa. As is current practice, <strong>the</strong> electric conductivity and, consequently, photocatalyticactivity (PCA), are increased by alloying TiO 2 with donor substitutional impurities. In P25,this impurity is OH – whose content, proceeding from loss on ignition, corresponds to aconcentration <strong>of</strong> about 7.8·10 20 cm –3 , which exceeds conventional concentrations by an order<strong>of</strong> magnitude. However, in P25 <strong>the</strong>y are distributed unevenly since it contains 10-20% <strong>of</strong>rutile. It can be surmised that <strong>the</strong> rutile PCA is not maximally possible.The work aims at creating effective and <strong>the</strong>rmally stable photocatalysts on <strong>the</strong> basis <strong>of</strong>nano-size powders alloyed with TiO 2 anion impurities.The samples were obtained by low-temperature hydrolysis <strong>of</strong> titanium salts in ammoniawater containing weighed amounts <strong>of</strong> F – or PO 3– 4 anions. Thermal treatment was carried outat 60-1150 °C. The resulting samples were characterized relatively unalloyed ones (Cl) byBET, XPA and SEM microscopy. Their PCA was assessed by <strong>the</strong> level <strong>of</strong> degradation <strong>of</strong>brightly-red ferroine (FEK-56 PM) reduced in daylight.The even distribution <strong>of</strong> alloying ions in <strong>the</strong> resulting anatase (XPA) in quantities <strong>of</strong>1÷7·10 20 аt·сm –3 sustains a developed surface (250-50 m 2·g –1 ) <strong>of</strong> <strong>the</strong> alloyed samples up to <strong>the</strong>calcination temperature <strong>of</strong> 700-900 °C.The PCA <strong>of</strong> alloyed TiO 2 increases in <strong>the</strong> impurity series Cl – 3–, PO 4 and F - , beingcomplexly affected both by impurity content and treatment temperature. As shown by SEM,<strong>the</strong> decisive effect on <strong>the</strong> forming morphology is that <strong>of</strong> <strong>the</strong> nature <strong>of</strong> <strong>the</strong> anion. The F-surface<strong>of</strong> <strong>the</strong> samples is homomorphous and highly dispersive up to <strong>the</strong> temperature <strong>of</strong> rutilization.In <strong>the</strong> region <strong>of</strong> 400-500 °C <strong>the</strong> PCA diminishes probably due to restructuring <strong>of</strong> fluorinatedanatase (according to XPA). The PCA <strong>of</strong> F – 3–and PO 4 modified TiO 2 did not change in <strong>the</strong>450

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