Enhanced Photoactivity of V鈭扤 Codoped TiO2 Derived from a Two-Step Hydrothermal Procedure for the Degradation of PCP鈭扤a under Visible Light Irradiation
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文摘
A new route to synthesize V-doped and V鈭扤 codoped titania nanocatalysts using a novel two-phase hydrothermal method applied in hazardous PCP鈭扤a decomposition was reported. The physicochemical properties were characterized, indicating that the crystallite surface area increased after both first hydrothermal (FH) V impregnation and second hydrothermal (SH) N implantation, whereas mesoporous framework shrinkage and enlargement resulted from FH and SH, respectively. ICP and EPR demonstrated that SH did not alter V content, but rather it induced paramagnetic V4+ increase. The V species was enhanced from the inner to the catalyst surface with V5+ as the dominant mode and the N dopant existed with substitutional nitrogen as the main structure. The optical red shift by low vanadium implantation was ascribed to the V2p state, mainly from V4+ species in the matrix. After SH incorporation, the substitutional N1s state, interstitial N鈭扥 state, and concomitant NOx were responsible for the strong visible absorption of V鈭扤鈭扵iO2. The photodegradation rates of PCP鈭扤a by the remodified catalysts after SH were much larger than that of the mono-V-TiO2 precursors fabricated in FH. SHNV02, SHNV05, and SHNV10 exhibited 2.4, 1.6, and 3.1 times promotion toward PCP鈭扤a decomposition, respectively. Moreover, other variations and the synergetic effects after two-phase treatments were adequately discussed and proven to be useful in facilitating photocatalytic promotion. This work provided a strategy for obtaining further enhancement of the synthesized catalyst by second-step modification to achieve the deep removal effect of contaminants.

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