Preparation of Bentonite Supported Nano Titanium Dioxide Photocatalysts by Electrostatic Self-assembly Method

Electrostatic self-assembly method （ESAM） was used to prepare bentonite supported-nano titanium dioxide photocatalysts. The materials were characterized by X-ray diffraction （XRD）, fourier transform infrared spectroscopy （FT-IR） and scanning electron microscopy （SEM）. Methyl orange was used to estimate the photocatalytic activity of the materials. The effects of the calcination temperature and silane dosage on the photocatalytic activity of the samples were investigated. The experimental results show that the bentonite facilitates the formation of anatase and restrains the transformation of anatase to rutile. Part of nano-size TiO2 particles insert into the galleries of bentonite. The photocatalysts exhibit a synergistic effect of adsorption and photocatalysis on methyl orange. Photocatalysts prepared by ESAM method exhibit higher photocatalytic activity and better recycle ability than those of the traditional method.

The Promoting Effect on the Activities ofFe Doped TiO_2 Photocatalysts

The particles of titanium-iron (Ti/Fe) complex with different Fe contents were prepared by means of the sol-gel method and used as a photocatalyst. The activity of the catalyst was investi- gated as a function of the Fe content during the liquid-phase oxidation of tetracycline, which showed an enhancement at the low Fe content. The XRD, Raman, XPS, and UV-Vis absorp- tion spectra indicated that the crystalline structure of the Ti/Fe complex particles changed from anatase phase to rutile phase when the Fe content increased. The isolated Fe203, Fe304, FeO species were observed and Fe3+ ions were highly dispersed in the TiO2 matrixes, then Ti-O-Fe species were formed. These species increased the surface defects of the Ti/Fe particles. Also, ac- tive hydroxyl radicals could be generated in the catalytic transformation, which led to the higher activity of the catalyst than bare Ti02 for the degradation of tetracycline.

Cu/TiO_(2) Photocatalysts for CO_(2) Reduction: Structure and Evolution of the Cocatalyst Active Form

Extensive work on a Cu-modified TiO_(2) photocatalyst for CO_(2) reduction under visible light irradiation was conducted. The structure of the copper cocatalyst was established using UV-vis diff use refl ectance spectroscopy, high-resolution transmis- sion electron microscopy, X-ray absorption spectroscopy, and X-ray photoelectron spectroscopy. It was found that copper exists in different states (Cu 0 , Cu^(+) , and Cu^(2+) ), the content of which depends on the TiO_(2) calcination temperature and copper loading. The optimum composition of the cocatalyst has a photocatalyst based on TiO_(2) calcined at 700℃ and modified with 5 wt% copper, the activity of which is 22 μmol/(h·g cat ) (409 nm). Analysis of the photocatalysts after the photocatalytic reaction disclosed that the copper metal on the surface of the calcined TiO_(2) was gradually converted into Cu_(2) O during the photocatalytic reaction. Meanwhile, the metallic copper on the surface of the noncalcined TiO_(2) did not undergo any trans- formation during the reaction.

Preparation of V-doped TiO_2 Photocatalysts by the Solution Combustion Method and Their Visible Light Photocatalysis Activities

A series of nanocrystalline V-doped （0.0-3.0 at.%） TiO2 catalysts have been successfully prepared by the one-step solution combustion method using urea as a fuel. The obtained powders were characterized by XRD, SEM, Raman, XPS and UV-Vis DRS. The effects of V doping concentration on the phase structure and photocatalytic properties were investigated. XRD, Raman, and XPS show that V doping diffuses into TiO2 crystal lattice mainly in the form of V5＋ and causes a phase transition from anatase to mille. V doping can widen the light absorption range of TiO2, with the absorption threshold wavelength shifting from 425 to 625 nm. The photocatalytic activity of V-doped TiO2 powders were evaluated by the photocatalytic degradation of methyl orange （MO） under visible light irradiation. It is found that V doping enhances the photoeatalyilc activity under visible light irradiation and the optimal degradation rate of MO is about 95.8% with 1.0 at% V-doped TiO2.

New Preparation Method of Visible Light Responsive Titanium Dioxide Photocatalytic Films

We report a new and simple preparation method of the visible light responsive Titanium dioxide (TiO2) photocatalytic films using sol-gel method and ultraviolet light (UV) irradiation. Proposed films were prepared on fused silica plates using titanium tetra-isopropoxide, urea, 2-methoxyethanol, water and UV irradiation. The 650°C-annealed films were carbon-containing anatase type TiO2, not carbon-doped ones. The prepared films absorbed visible light with wavelengths longer than 400 nm. Also, organic dyes were effectively photodegradated by visible light irradiation in the presence of these films.

Synthesis and photocatalytic properties of lanthanum doped anatase TiO_2 coated Fe_3O_4 composites

A composite photocatalyst （La/TiO2/Fe3O4） with a lanthanum doped TiO2 （La/TiO2） shell and a magnetite core was prepared by coating photoactive La/TiO2 onto a magnetic Fe3O4 core. The morphological, structural, and optical properties of as-prepared samples were charac-terized by transmission electron microscopy （TEM）, X-ray diffraction （XRD） and UV-vis absorption spectroscopy. The effect of lanthanum content on the photocatalytic properties was studied, and the result revealed that 0.15 mol% La/TiO2/Fe3O4 exhibited the highest photoactiv-ity. The photocatalytic properties of the prepared photocatalyst under UV and visible light were investigated in aqueous solution using methyl orange （MO） as a target pollutant. The results showed that the prepared photocatalyst was activated by visible light and used as an ef-fective catalyst in photooxidation reactions. In addition, the possibility of cyclic usage of the prepared photocatalyst was also confirmed. Moreover, La/TiO2 was tightly bound to Fe3O4 and could be easily recovered from the medium by a simple magnetic process.

Preparation and characterization of in-site regenerated TiO_2-ACFs photocatalyst

In-site regenerated titanium dioxide-activated carbon fibers （TiO2-ACFs） photocatalyst was prepared by the sol-gel method. De-tailed surface and structural characterization of the TiO2-ACFs photocatalyst was carried out. The photoactivity of TiO2-ACFs under ultra-violet irradiation was compared with original ACFs and pure TiO2 by the degradation of methylene blue aqueous solution. The degradation efficiency by the TiO2 （5wt%）-ACFs sample is much higher than that by TiO2 and ACFs. The results show that the photocatalysis by TiO2-ACFs is a six-step process. The adsorption-transfer-photocatalysis rate of TiO2-ACFs is higher than the adsorption-photocatalysis rate of TiO2, so the photocatalysis rate of the TiO2-ACFs system is higher than that of TiO2 photocatalyst.

A visible light-responsive iodine-doped titanium dioxide nanosphere

I-doped titanium dioxide nanospheres （I-TNSs） were synthesized via a two-step hydrothermal synthesis route, their potential for the efficient utilization of visible light was evaluated. The prepared anatase-phase I-TNSs had a bimodal porous size distribution with a Brunauer-Emmett-Teller surface area of 76 m2/g, a crystallite size of approximately 14 nm calculated from X-ray diffraction data, and a remarkable absorption in the visible light region at wavelengths 〉 400 nm. The photocatalytic activity of the samples was evaluated by decoloration of Methyl Orange in aqueous solution under visible light irradiation in comparison to the iodine-doped TiO2 （I-TiO2）. The I-TNSs showed higher photocatalytic efficiency compared with I-TiO2 after irradiation for 180 rain even though the latter had a much greater surface area （115 m2/g）. It was concluded that the surface area was not the predominant factor determining photocatalytic activity, and that the good crystallization and bimodal porous nanosphere structure were favourable for photocatalysis.

Preparation and characterization of nitrogen-doped titanium dioxides

A type of high visible-light active titanium oxinitride(TiO2-xNx) powder was prepared by a simple proc-ess:the calcination of the hydrated titanium dioxide at the atmosphere of ammonia-argon using a tu-bular electric furnace at high temperatures. The hydrated titanium dioxide was synthesized as the precursor of TiO2-xNx using titanic acid as raw material,which came from sulfate technique of produc-ing titanium white. The effects of temperature and reaction time on the nitrogen content,grain size and crystal structure were studied. The visible-light activity and photocatalysis capability of the powder were also investigated.

Preparation and visible-light photocatalytic property of nanostructured Fe-doped TiO_2 from titanium containing electric furnace molten slag

Nanostructured Fe-doped titanium dioxide was synthesized from titanium containing electric furnace molten slag （TCEFMS） by using an alkali fusion, followed by a hydrolyzation-acidolysis-cMcination route. The effects of Mkali/slag mass ratio, calcinating temperature, calcinating time, and water/slag mass ratio on the extraction efficiency and purity of products were systematically studied in this paper. It is indicated that the best extraction efficiency of nanostructured Fe- doped titanium dioxide is 99.35%, when the molten slag is calcinated at 700℃ for 1 h with the mass ratio of alkali/molten slag of 1.5：1. The influence of alkali/slag mass ratio on the photocatalytic activity of final products was evaluated by the photodegradation of methyl blue under visible light irradiation. A maximum photodegradation efficiency of 88.12% over 30 min was achieved under the optimum conditions.

Antibacterial Properties of V-doped Titanium-bearing Blast Furnace Slag Prepared at Different Calcination Temperatures

Perovskite-type V-doped titanium-bearing blast furnace slag (VTBBFS) photocatalyst was prepared by high-temperature solid phase method.The influence of calcination temperature on the photocatalytic and antibacterial properties of VTBBFS was studied in details.Its composition and microstructure were evaluated by X-ray diffractometer,ultraviolet-visible absorption spectrometer,Fourier transform infrared spectrometer and scanning electron microscope.The antibacterial properties of VTBBFS to Candida albicans were investigated by flask oscillation method.The results showed that the optical absorption and antibacterial properties of VTBBFS were the best with 10%(ω) doping of vanadium,prepared at 800℃ for 2 h,and its sterilization rate was close to 100% to Candida albicans (ATCC10231).The minimum inhibitory and minimum bactericidal concentrations were 25 and 50 mg/mL.When the concentration was 0.2 μg/mL,the catalyst had the least toxic toxicity.

Facile Preparation and Visible-light Photocatalysis Enhancement of N-Doped β-TiO_2 Nanobelts

A facile preparation of nitrogen-doped β-TiO2（N-doped β-TiO2） nanobelts and their visible-light photocatalytic activity were reported.The preparation of N-doped β-TiO2 nanobelts consisted of cation-exchange between layered sodium titanate nanobelts and NH 4 ＋ in aqueous solution at room temperature and subsequent calcination in air.Such a calcination treatment is beneficial to the formation of monoclinic N-doped β-TiO2 nanobelts.Various measurement results indicate that not only were the nitrogen atoms doped into the lattice of β-TiO2 nanobelts resulting in a strong visible-light absorption,but also a large number of defects were caused by them in the lattice,increasing the stability of β-TiO2.The photocatalysis enhancement of N-doped β-TiO2 nanobelts for the photodegradation of Rhodamine B was demonstrated.

Preparation and characterization of (metal, nitrogen)-codoped TiO_2 by TiCl_4 sol-gel auto-igniting synthesis

The nitrogen-doped and （metal, nitrogen）-codoped TiO2 photocatalysts （metal = Ag, Ce, Fe, La） were synthesized by sol-gel auto-igniting synthesis （SAS） with the complex compound sol of TiCl4-NH4NO3-citri acid-metal nitrate- NH3.H20 as a precursor. The products were characterized by means of XRD, XPS, and UV-Vis diffuse reflectance spectra, and their photocatalytic activity was investigated under visible light. It was found that all the synthesized powders showed good absorption for visible light, and that the radius and alterable valence states of doping metallic cations played important roles on their photocatalytic activity. These results were discussed in detail.

Synthesis,characterization,and theoretical study of N,S-codoped nano-TiO_2 with photocatalytic activities

Nitrogen and sulfur doped titanium dioxide photocatalysts were prepared by the sol-gel method.The products were characterized by X-ray diffraction （XRD）,transmission electron microscopy （TEM）,and UV-visible diffuse reflectance spectra （DRS）.Photocatalytic activities of the samples were investigated on the degradation of methyl orange （MO）.The effect of the dopants on the electronic structure of TiO2 was studied by the first-principles calculations based on the density functional theory （DFT）.The orbital hybridization resulted in energy gap narrowing and electronic delocalization in the crystal of doped TiO2.Mobile electrons of varied energetic states could offer enhanced electron transfer,together with optical absorption improvement.The results show that the doping elements of N and S play a cooperative role in the modification of electronic structure,which enhances the photocatalytic performance.The experimentally observed absorption edges of N-doped TiO2,S-doped TiO2,and N,S-codoped TiO2 are 420,413,and 429 nm,respectively,which can be explained by the theoretical calculation results.

N-TiO_(2)/聚丙烯复合熔喷非织造材料的制备及其光催化性能

为制备具有光催化功能的聚丙烯(PP)熔喷非织造材料,首先通过溶胶-凝胶法制备氮掺杂二氧化钛(N-TiO_(2))光催化剂,然后采用超声浸渍的方法将N-TiO_(2)均匀负载在PP熔喷非织造材料表面得到N-TiO_(2)/PP复合熔喷材料,并对其结构和性能进行表征和分析,通过自由基捕获实验确定光催化机制。结果表明:N掺杂量为1%的N-TiO_(2)的颗粒大小均匀,粒径约为10 nm,在30 min暗吸附和90 min光照条件下,其光催化降解亚甲基蓝(MB)的效率最佳,达到98%;将该N-TiO_(2)负载在PP熔喷非织造材料表面后,可包裹在PP纤维表面,当负载量超过30 mg后出现团聚现象;负载量为30 mg的N-TiO_(2)/PP复合熔喷材料的光催化降解性能最优,在30 min暗吸附和90 min光照条件下,对亚甲基蓝(MB)的降解效率达到98%;在光激发下N-TiO_(2)会产生超氧自由基和羟基自由基,二者共同降解MB。

Enhanced photocatalytic activity of (La, N) co-doped TiO_2 by TiCl_4 sol-gel autoigniting synthesis

（La, N） co-doped TiO2 photocatalysts were synthesized using TiC14 sol-gel autoignidng synthesis （SAS） starting from a complex compound system of TiCl4-La（NO3）3-citric acid-NH4NO3-NHyH2O, in which the （La, N） co-doped process was accompushed in the formation of TiO2 nanocrystals. The prepared samples were characterized by using X-ray diffraction （XRD）, X-ray photoemission spectroscopy （XPS） and UV-vis diffuse reflectance spectra. The results indicated that nitrogen and lanthanum were incorporated into the lattice and interstices of titania nanocrystals, which resulted in narrowing the band gap and promoting the separation of photoexcited hole-electron pairs, respectively, and showing expected red-shifts and enhanced photocatalytic activity under visible light. The mechanism on nitrogen doping and enhancement in photocatalyfic activity of （La, N） co-doped titania by SAS was discussed in detail.