In-situ synthesis and photocatalytic properties of ilmenite-based potassium titanate composites
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1.College of Vanadium and Titanium, Panzhihua University, Panzhihua 617000 , China ;2.Vanadium and Ti-tanium Resource Comprehensive Utilization Key Laboratory of Sichuan Province, Panzhihua 617000 , China ;3.Sichuan Provincial Engineering Laboratory of Solar Technology Integration, Panzhihua 617000 , China ;4.State Key Testing Laboratory of Vanadium & Titanium, Panzhihua 617000 , China

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TF125;TF823

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    Abstract:

    In this paper, titanium concentrate and anhydrous potassium carbonate were used as raw materials to synthesize potassium ferrite composites in situ by oxidation roasting process. The roasted products prepared at different roasting temperatures were characterized and their photocatalytic degradation performance was evaluated. The phase composition, valence state, spectral absorption and microscopic morphology of the roasted products were characterized by XRD, XPS, UV-Vis and SEM. The results show that the calcined product after oxidation roasting is mainly composed of potassium ferrite, potassium titanate and potassium titanium ferrite. Potassium ferrite and potassium titanate are unevenly attached to the surface of potassium titanium ferrite crystal; iron and titanium exist in the form of Fe3+ and Ti4+, respectively; When the calcination temperature is 750℃, 850℃ and 950℃, the band gaps of the synthesized potassium titanate composites are 1.25eV, 1.15eV and 1.45eV, respectively; photocatalytic performance test results show that with the increase of calcination temperature, the photocatalytic degradation performance of calcined products for methylene blue first increases and then decreases, and the potassium titanoferrite composites at 850℃ reach the optimum, up to 98.3%; when methyl orange is used as a pollutant, the degradation effect of calcined products is better with the increase of calcination temperature, and the degradation rate can reach 56.6% at 1000℃.

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彭文静,吴恩辉,李军,等.钛铁矿基钛铁酸钾复合材料的原位合成及其光催化性能研究[J].中国有色冶金,2024,53(6):41-49.

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  • Received:September 16,2024
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  • Online: December 21,2025
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