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In this paper, zinc calcines, sulfuric acid, ferric nitrate nine-hydrate, zinc nitrate hexahydrate, titanium oxide sulfate, sodium hydroxide and ammonia water were selected as raw materials, and the methods of sulfuric acid leaching and chemical coprecipitation were used to prepare purified zinc ferrite, synthetic zinc ferrite, synthetic titanium dioxide and its composite with purified zinc ferrite. And characterized by BET, UVVis and FTIR. The results showed that: SO42- existed in purified zinc ferrite. Purified zinc ferrite, synthetic zinc ferrite and purchased had different specific surface area, pore volume and average pore size. The specific surface area of synthetic zinc ferrite decreased with the increase of calcination temperature. The three kinds of zinc ferrite had good absorption of ultraviolet light and visible light. Purchased ferric acid had the strongest absorption of UV light and synthetic zinc ferrite had the strongest absorption of visible light, and purified zinc ferrite had the absorption of UV light and visible light between the two. The specific surface area of titanium dioxide prepared by chemical coprecipitation method was greatly affected by calcination temperature. With the increase of calcination temperature, the specific surface area decreased from 123.633 to 28.036m2·g-1, and the average pore diameter was less affected by calcination temperature. For the zinc ferrite/titanium dioxide composite prepared by chemical coprecipitation method, a certain amount of purified zinc ferrite was added to facilitate the absorption of visible light by titanium dioxide.

In this paper, sulfuric acid leaching high iron zinc calcine was used to prepare and purify zinc ferrite, high temperature roasting method was used to prepare synthetic zinc ferrite, and sol-gel method was used to prepare TiO2. The properties of the prepared samples ware characterized by XRD, FT-IR, BET, SEM and other methods. The results show that the synthetic zinc ferrite is pure zinc ferrite, and the purified zinc ferrite contains impurities PbSO4. The TiO2 crystal form prepares at the calcination temperature of 300~550°C is basically the same, and the crystal form transformation occurs at the calcination temperature of 550~600°C. TiO2 samples calcines at 400°C (T400) have higher specific surface area, larger total pore volume and average pore diameter. The crystalline degree of synthetic zinc ferrite is high, the micropores on the crystal surface are closed, and the grains bond with each other. The specific surface area, total pore volume and average pore diameter of purified zinc ferrite are larger than those of synthetic zinc ferrite. The effects of specific surface area, pore volume and pore structure on the adsorption capacity and catalytic efficiency are as follows: T400> purified zinc ferrite > synthesized zinc ferrite.

In this paper, the methods of sulfuric acid leaching and chemical coprecipitation were used to prepare products such as purified zinc ferrite, synthetic zinc ferrite, synthetic titanium dioxide and its complex with purified zinc ferrite. The morphology and microstructure of the above samples were characterized and analyzed by XRD and SEM. The results showed that the purified zinc ferrite contained a small amount of ZnO, SiO2, Al2O3 and PbSO4. Its particle size was the largest and the crystallinity was the best, but the surface was not smooth, the particle size distribution was not uniform and there was agglomeration phenomenon. The purchased zinc ferrite had high purity, the smallest particle size and the worst crystallinity. Its surface was smooth, particle size distribution was uniform, and it was loose and porous. The synthetic zinc ferrite had high purity, smooth surface, uniform particle size distribution and obvious agglomeration. The prepared titanium dioxide had no other impurities, good crystallinity, smooth surface and certain agglomeration phenomenon. For the zinc ferrite/titanium dioxide composite, adding a small amount of purified zinc ferrite would change the crystallinity of titanium dioxide, but it had little effect on the grain size of titanium dioxide. The surface was rough, the particle size distribution was not uniform, and there was agglomeration phenomenon.