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A string of niobium-iron composite oxides with varying Nb/Fe ratios and calcination temperatures were produced and utilized to remove mixed contaminants (500 ppmv chlorobenzene and 500 ppmv toluene in air), and the structure/texture of catalytic materials were systematically characterized. The findings of the structure-performance study revealed that the physicochemical qualities of Nb 2 O 5 -Fe 2 O 3 were greatly enhanced than pure metal oxide. The presence of iron oxide hindered the crystallization of niobium oxide, which aided in the uniform dispersion of niobium-iron components into each other. Forming FeNbO 4 at Nb/Fe molar ratio of 1/2 effectively improved the thermal stability of catalyst, withstood short-time thermal shock below 850 °C. The formation of niobium-iron composite oxides improved the specific surface area, optimized the pore size distribution, increased surface acid centers, enhanced reduction/oxidation cycle, and promoted metal-metal interaction for the Nb-Fe-O catalysts. At 320 °C, the catalytic degradation efficiency of 1Nb2Fe-500 could approach 90% for chlorobenzene and 85% for toluene, and it could sustain this efficiency for at least 80 h without evident deactivation, with a high CO 2 selectivity of 86%. Furthermore, the Nb-Fe-O catalysts met the environmentally benign and low-cost requirements for environmental catalysis. [Display omitted] • The Nb-Fe composite oxides were synthesized and structure/texture were characterized. • The formation of FeNbO 4 was an important factor affecting the catalyst activity. • 1Nb2Fe-500 exhibited high performance for eliminating mixture of C 6 H 5 Cl and C 6 H 5 CH 3. • The 1Nb2Fe-500 catalyst could withstand thermal shock below 800 °C. [ABSTRACT FROM AUTHOR]

Transition metal doped WO 3 mixed oxides (named as W-M-O, M = Nb, Fe, Cr, Cu, Ti or Sn, respectively) with high structure stability were synthesized by modified sol-gel method using citric acid as organic crosslinking agent, and were evaluated for catalytic elimination of low-concentration toluene, monochlorobenzene and 1,2-dichloroethance with high toxicity and relatively stable molecule structure, as the typical examples for the pollutants of various volatile organic compounds (VOCs). Results of the structure-property-performance relationship research showed that mesoporous structure and nanocrystalline/amorphous state were formed, and binary metal components were dispersed into each other, which contributed to promoting the metal/metal electron interaction and adjusting the physicochemical properties of mixed metal oxides. The sequence of apparent catalytic activity for toluene degradation was: W–Nb–O＞W–Fe–O＞W–Cr–O, W–Cu–O＞W–Ti–O＞W–Sn–O＞WO 3 , and the sequence for monochlorobenzene degradation was: W–Nb–O＞W–Fe–O＞W–Cr–O, W–Ti–O＞W–Cu–O＞W–Sn–O＞WO 3. There existed cooperative catalytic effect: mesopore and surface acid sites of catalysts facilitated adsorption, activation and breakage of the C-X bond, and then redox sites of catalysts promoted deep oxidation of a series of reaction intermediates to transform into CO 2 and H 2 O. Especially, the optimized W–Nb–O catalyst deserved more attention, since it represented remarkable catalytic activity, selectivity and durability for three typical VOCs degradation along with good resistance to water vapor and corrosion of HCl. [Display omitted] • WO 3 based transition metal mixed oxides were prepared by modified sol-gel method. • Interaction between WO 3 and MO x affected the properties of mixed oxides. • WO 3 –Nb 2 O 5 displayed the best catalytic performance for VOCs elimination. • Cooperative catalytic effect was observed in WO 3 –Nb 2 O 5 catalyst system. [ABSTRACT FROM AUTHOR]