Studies on preparation and characterization of 3DOM TiO2 and TiO2/SiO2 materials with high photocatalytic ability

In this paper, three-dimensional ordered macroporous (3DOM) TiO₂ and TiO₂/SiO₂ materials were prepared by traditional colloidal-crystal-templating method. The microstructures of samples were analysed by scanning electron microscope, X-ray diffraction analysis, thermogravimetric-differential thermal analysis and nitrogen adsorption/desorption. The results indicated that the microstructures of samples, including three-dimensional ordered macroporous structure and crystalline form, could be adjusted by changing the calcination temperatures. Finally, the samples were used as photocatalysts to decompose methyl orange wastewater under UV-light. Both 3DOM TiO₂ and 3DOM TiO₂/SiO₂ displayed good photocatalytic ability. Moreover, the introduction of Si could increase the transformation temperature of TiO₂ from anatase to rutile, which made 3DOM TiO₂/SiO₂ had better photocatalytic ability than pure 3DOM TiO₂.     

Photocatalytic Properties of Silica-supported TiO2

TiO₂ supported on SiO₂ surface is effective on the recovery of photocatalyst, morphological control, and coating on the substrate. Furthermore, it shows much higher photocatalytic activity than pure TiO₂. The silica support is quite influential on the surface properties of TiO₂ supported on SiO₂. The enhanced photocatalytic activity of TiO₂–SiO₂ could be explained by the effects of surface area, adsorption, band-gap energy and local structure. However, it is difficult to say which one is the most important factor responsible for the photocatalytic property of TiO₂–SiO₂. For example, the reduction of particle size could effect on both of the surface area and band-gap energy. And, Ti–O–Si bonds could modify the band-gap energy and local structure. Therefore, the photocatalytic properties of TiO₂–SiO₂ should be expressed by sum of many factors such as surface area, adsorption, band-gap energy and local structure.     

Direct Solvothermal Formation of Nanocrystalline TiO2 on Porous SiO2 Adsorbent and Photocatalytic Removal of Nitrogen Oxides in Air over TiO2–SiO2 Composites

Solvothermal decomposition of titanium(IV) tert-butoxide (TTB) in toluene at 573 K in the presence of silica gel (SiO₂) with continuous stirring yielded a titanium(IV) oxide (TiO₂)–SiO₂ composite in which agglomerates of nanocrystalline TiO₂ were deposited on the surfaces of SiO₂ particles. Various TiO₂–SiO₂ composites having different TiO₂ contents can be synthesized by changing the ratio of TTB and SiO₂, and the composites had large surface areas corresponding to porous properties of SiO₂. These TiO₂–SiO₂ composites were used for photocatalytic removal of nitrogen oxides in air and their photocatalytic performances were compared with those of other TiO₂–SiO₂ samples prepared by different methods. Solvothermally synthesized 74 wt.%TiO₂–SiO₂ composite exhibited excellent photocatalytic performance (almost stoichiometric removal of NO _x (98%) and very low NO₂ release (0.3%)) attributable to high photocatalytic activity of TiO₂ and high adsorption property of SiO₂. Lesser performance of 74 wt.%TiO₂–SiO₂ composites prepared by other methods suggested that pore-mouth plugging of SiO₂ by TiO₂ and lower level of mixing of TiO₂ and SiO₂ decreased photocatalytic performance of the composites.     

Core@dual‐Shell Nanoporous SiO2–TiO2 Composite Fibers with High Flexibility and Its Photocatalytic Activity

Structural design is of great importance to the performance of photocatalysts in environmental remediation. Therefore, micro/nanofibrous morphology and nanoporous local structures have been found to be beneficial to improve the photocatalytic activity. In this investigation, we report the design and fabrication of flexible and thermal stable nanoporous SiO₂–TiO₂ composite fibers as efficient photocatalysts. Combining electrospinning and modified Stöber techniques, core‐shell and mesoporous SiO₂ fibers with high flexibility were fabricated and employed as the scaffold for supporting TiO₂ nanoparticles. A nanoporous shell of TiO₂ nanoparticles was then muffled over the SiO₂ fibers to form core@dual‐shell SiO₂–TiO₂ composite fibers with hierarchically porous structure, which were conveniently patterned into a nonwoven, recyclable film. This nonwoven film exhibits better photocatalytic activity for Rhodamine B degradation under UV irradiation compared with some other TiO₂‐based materials reported in recent years.     

Photoassisted mineralization of remazole red F3B over NiO/TiO2 and CdO/TiO2 nanoparticles under simulated sunlight

In this work, a series of titania-supported NiO and CdO materials were synthesized by a modified sol-gel process. The prepared photocatalysts were characterized by X-ray diffraction (XRD), UV-Vis diffuse reflectance spectroscopy (DRS), and transmission electron microscopy (TEM). The activities of titania-supported NiO and CdO photocatalysts for photocatalytic degradation of Remazole Red F3B (RR) dye, under simulated sunlight, were investigated. The photocatalytic mineralization of an RR dye solution over various NiO-x/TiO₂ and CdO-x/TiO₂ photocatalysts under simulated sunlight was investigated. It was worthy noticing that the photocatalytic activity of titania improved using the prepared catalysts. The prepared TiO₂, NiO-5/TiO₂, and CdO-2/TiO₂ photocatalysts exhibited higher photocatalytic activity under simulated sunlight than did commercial TiO₂. The prepared photocatalysts were stable after photocatalytic degradation of the dye. The observed photocatalytic mineralization of the dye was 51 and 71% over NiO-10/TiO₂ and CdO-2/TiO₂ after 180 min of irradiation, respectively. Juxtaposing a p-NiO-5/TiO₂ semiconductor provided a potential approach for decreasing charge recombination. The prepared photocatalystsNiO-5/TiO₂ and CdO-2/TiO₂ are promising composites for the solar detoxification of textile wastewater.     

Photocatalytic activity of metal-decorated SiO<Subscript>2</Subscript>@TiO<Subscript>2</Subscript> hybrid photocatalysts under water splitting

We report the fabrication of a metal-decorated hybrid nanocomposite with TiO₂ encapsulation (Metal/SiO₂@TiO₂, Metal=Pt or Ru) using a simple surface-modification chemical process. Metal nanoparticles capped with polyvinylpyrrolidone were successfully assembled on functionalized SiO₂ via electrostatic interactions, after which a thin layer of TiO₂ was coated on the surface by the sol-gel process to avoid agglomeration of the coated silica spheres. Transmission electron microscopy studies confirmed that the metal nanoparticles were uniformly distributed throughout the surface of the SiO₂ with a thin layer of TiO₂. In addition, X-ray diffraction was employed to ensure the crystal structure of the uniformly coated thin TiO₂ layer. Even after calcination at 500 °C, the structure remained intact, confirming high thermal stability. The photocatalytic activity of the metal-decorated SiO₂/TiO₂ nanocomposites was evaluated using the H₂ evolution reaction. The Metal/SiO₂@TiO₂ catalysts show the photocatalytic water splitting efficiency for H₂ generation (i.e., 0.14% for Pt/SiO₂@TiO₂ and 0.12% for Ru/SiO₂@TiO₂), while there is no generation of H₂ on the Metal/SiO₂ without a coating layer. These results indicate that the anatase crystalline coating layer has good thermal and chemical stability and plays a significant role in photocatalytic H₂ production.     

Fabrication of superhydrophilic self-cleaning SiO2–TiO2 coating and its photocatalytic performance

Generally, superhydrophilic self-cleaning coatings are prepared from semiconductors with photocatalytic properties. Organic pollutants attached to the coating surface can be degraded by its photocatalytic performance realizing a self-cleaning goal. Herein, SiO₂–TiO₂ composite particles were fabricated by the hydrolysis and precipitation of TiOSO₄, and SiO₂ microspheres were chosen as carriers, which are inexpensive and environmentally friendly. Then, superhydrophilic self-cleaning SiO₂–TiO₂ coatings were fabricated by spraying the composites on the surfaces of substrates. The morphology, structure and self-cleaning performance of the SiO₂–TiO₂ coating were characterized and tested. The results revealed that nano-TiO₂ was loaded on the surfaces of SiO₂ microspheres uniformly forming a hierarchical micro/nanostructure. The SiO₂–TiO₂ composite particles exhibited excellent photocatalytic degradation performance, and the degradation rate of methyl orange (10 ppm) was more than 98% under UV irradiation for 40 min. Furthermore, the coating prepared with the SiO₂–TiO₂ composite particles exhibited superhydrophilicity. A water droplet spreads completely on the coating surface in 0.35 s, and the contact angle reaches 0°. In addition, rhodamine B (RhB) and methylene blue (MB) on the coating surface can be degraded efficiently under sunlight irradiation. The SiO₂–TiO₂ composite particles can be sprayed directly on the surfaces of concrete, brick, wood, and glass slides. Therefore, the particles showed good adaptability to different substrates. The superhydrophilic property was due to the hydrophilicity of SiO₂ and TiO₂, the hierarchical micro/nanostructure of the SiO₂–TiO₂ composites, and the photoinduced superhydrophilicity of TiO₂. The above experimental results show that the as-prepared superhydrophilic self-cleaning SiO₂–TiO₂ coating has a large application potential.     

Preparation of hydrophobic SiO<Subscript>2</Subscript>@(TiO<Subscript>2</Subscript>/MoS<Subscript>2</Subscript>) composite film and its self-cleaning properties

TiO₂/MoS₂ composite was encapsulated by hydrophobic SiO₂ nanoparticles using a sol–gel hydrothermal method with methyltriethoxysilane (MTES), titanium tetrachloride (TiCl₄), and molybdenum disulfide (MoS₂) as raw materials. Then, a novel dual functional composite film with hydrophobicity and photocatalytic activity was fabricated on a glass substrates via the combination of polydimethylsiloxane adhesives and hydrophobic SiO₂@(TiO₂/MoS₂) composite particles. The influence of the mole ratios of MTES to TiO₂/MoS₂ (M:T) on the wettability and photocatalytic activity of the composite film was discussed. The surface morphology, chemical compositions, and hydrophobicity of the composite film on the glass substrate were investigated by scanning electron microscopy, transmission electron microscopy, X-ray powder diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and water contact angle (water CA) measurements. The results indicated that the composite film exhibited stable superhydrophobicity and excellent photocatalytic activity for degradation of methyl orange (MO) even after five continuous cycles of photocatalytic reaction when M/T was 7:1. The water CA and degradation efficiency for MO remained at 154° and 94%, respectively. Further, the composite film showed a good non-sticking characteristic with the water sliding angle (SA) at about 4°. The SiO₂@(TiO₂/MoS₂) composite consisting of hydrophobic SiO₂ nanoparticles and TiO₂/MoS₂ heterostructure could provide synergistic effects for maintaining long-term self-cleaning performance.     

Synthesis,analysis and characterization of ordered mesoporous TiO2/SBA-15 matrix: Effect of calcination temperature

Mesoporous TiO₂/SBA-15 matrix was prepared by the sol–gel synthesis of TiO₂ in previously prepared SBA-15 particles. Nonionic surfactant was used as liquid template and Na₂SiO₄ as SiO₂ precursor for the synthesis of mesoporous silica SBA-15 with high specific surface area. Different calcination temperature was used for the synthesis and analysis of TiO₂/SBA-15 matrix. The synthesized titania/silica composites were characterized by X-ray diffraction, FTIR, TEM, UV–vis spectroscopy, etc. TEM micrographs showed titania is successfully embedded in SBA-15 channel. Different calcination temperature indicates different size of particle formation and different photocatalytic properties. The activity test indicated that TiO₂/SBA-15 composite prepared by this method had better photocatalytic performance than pure TiO₂. The preparation method and the textural characteristics of mesoporous materials have great influence for the photocatalytic activity.     

Photocatalytic performance of Ru doped anatase mounted on silica for reduction of carbon dioxide

Ru doped anatase supported on silica was prepared by solid-state dispersion method and examined for the photocatalytic reduction of carbon dioxide in aqueous medium at ambient conditions. To assist in interpreting the photocatalytic behaviour of Ru-TiO₂/SiO₂, reference systems consisting of Ru doped TiO₂ and TiO₂ supported on SiO₂ were also analyzed and the conditions were optimized. Ru/TiO₂ photocatalysts with metal loadings of 0.1, 0.3, 0.5 and 1.0 wt% were prepared by impregnation method and a series of TiO₂/SiO₂ catalysts with low TiO₂ (1, 3, 5 and 10 wt%) contents were prepared by solid-state dispersion method. The photocatalysts were characterized using X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), UV–vis DRS, FT-IR and Raman spectroscopy. The results showed that TiO₂ particles with Ru ions have higher photocatalytic activity than undoped TiO₂ and the optimum Ru loading was found to be 0.5 wt%. Nevertheless, the yield increased notably when TiO₂ was supported on SiO₂. This strong enhancement suggests that in 10 wt% TiO₂/SiO₂ the efficiency of charge separation is strongly influenced through the presence of TiOSi bridging bonds. On the contrary, Ru-TiO₂/SiO₂ has no significant improvement in activity over TiO₂/SiO₂ except that it shows nearly quadruple times higher activity for the formation of methanol than Ru/TiO₂. The difference in the photocatalytic activity is related to its physico-chemical properties.     

Preparation of oriented SiO32− doped TiO2 film and degradation of methylene blue under visible light irradiation

SiO₃^2? doped TiO₂ films with oriented nanoneedle and nanorectangle block structure has been firstly synthesized by hydrothermal synthesis method. The prepared samples are characterized, X-ray diffraction (XRD) results demonstrate that the SiO₃^2? doped TiO₂ films are rutile and brookite phases. The scanning electron microscope (SEM) analysis reveals that the quantity of O₂ affects the morphology of the SiO₃^2? doped TiO₂ films (SiTiA films prepared with unmodified substrate). The SiO₃^2? doped TiO₂ films (SiTiB films prepared with modified substrate) display two layers, one is porous structure, the other is nanoneedle structure. UV–vis, IR, transmission electron microscopy (TEM) and energy-dispersive X-ray (EDX) microscopy all prove that SiO₃^2? have been doped in the TiO₂ crystal structure. They have remarkable red shift and higher photocatalytic activity of degradation of methylene blue than P-25 under visible light (λ > 420 nm) irradiation. Besides, photocatalytic activity of the film is stable during 4 times recycling.     

Room Temperature Photocatalytic Oxidation of Carbon Monoxide Over Pd/TiO2–SiO2 Catalysts

The photocatalytic oxidation of carbon monoxide over TiO₂–SiO₂ and Pd/TiO₂–SiO₂ catalysts was studied. The catalyst samples were synthesized by using sol–gel technique coupled with hydrothermal treatment and all samples were hydrothermally treated before calcination in air. The catalyst samples were characterized by XRD, BET and DRIFTS techniques. The photocatalytic activity of the samples was determined by using circulated batch photoreactor coupled with in line gas transmission FTIR cell charged with 2,000 ppm carbon monoxide in air initially over 0.5 g of catalyst sample under 33 W (254 nm) irradiation power. XRD and BET results confirmed the presence of anatase phase and the decrease on the crystallite size of TiO₂ with SiO₂ addition which yield higher surface area and better dispersion of TiO₂ over mesoporous SiO₂. DRIFTS results indicated the presence of surface hydroxyls coordinated to Ti⁴⁺ and Si–O–Ti sites. All samples containing 10–90 % TiO₂ over SiO₂ exhibited significant photo oxidation activity at room temperature. The photocatalytic oxidation rate of carbon monoxide is favored by SiO₂ addition due to high surface area, better dispersion of TiO₂ particles and higher surface defects. The addition of PdO improves the photocatalytic activity significantly and the synergy between the TiO₂ and PdO phases.     

Effects of SiO2 addition on TiO2 crystal structure and photocatalytic activity

A series of TiO₂–SiO₂ mixtures – having the following stoichiometry Ti_1?xSi_xO₂, with x = 0, 0.1, 0.3 and 0.5 atoms per formula unit – were prepared by using precursor oxides and fired at three temperatures (900, 1000 and 1200 °C). The modifications in the structure and, consequently, on the photocatalytic activity, induced by the addition of SiO₂ into the TiO₂ powder, were thoroughly investigated by using various analytical techniques: X-ray powder diffraction, electron microscopy (FE-SEM and TEM), XPS, FT-IR, DRS and BET analysis. The results underlined as essentially no solid solution occurs between the two crystalline end-members. Nevertheless, silica addition caused a retarding effect on anatase-to-rutile phase transformation and on the crystallite growth.The photocatalytic activity of the powders was assessed in gas phase and the results were explained by taking into account the anatase and rutile relative amounts in the samples, their crystallite size, the surface hydroxyl groups adsorbed on the photocatalysts and the surface area of the mixtures.     

Engineering an ultrathin amorphous TiO2 layer for boosting the weatherability of TiO2 pigment with high lightening power

TiO₂ pigments are typically coated with inert layers to suppress the photocatalytic activity and improve the weatherability. However, the traditional inert layers have a lower refractive index compared to TiO₂, and therefore reduce the lightening power of TiO₂. In the present work, a uniform, amorphous, 2.9-nm-thick TiO₂ protective layer was deposited onto the surface of anatase TiO₂ pigments according to pulsed chemical vapor deposition at room temperature, with TiCl₄ as titanium precursor. Amorphous TiO₂ coating layers exhibited poor photocatalytic activity, leading to a boosted weatherability. Similarly, this coating method is also effective for TiO₂ coating with amorphous SiO₂ and SnO₂ layers. However, the lightening power of amorphous TiO₂ layer is higher than those of amorphous SiO₂ and SnO₂ layers. According to the measurements of photoluminescence lifetime, surface photocurrent density, charge-transfer resistance, and electron spin resonance spectroscopy, it is revealed that the amorphous layer can prevent the migration of photogenerated electrons and holes onto the surface, decreasing the densities of surface electron and hole, and thereby suppress the photocatalytic activity.     

P123 assisted morphology-engineered and hierarchical TiO<Subscript>2</Subscript> microspheres for enhanced photocatalytic activity

In this study, hierarchical titanium dioxide (TiO₂) microspheres with controlled morphology derived from calcination treatment of hierarchical titanate microspheres were fabricated. The obtained hierarchical TiO₂ microspheres with diameters of 1 to 2 µm were composed of polycrystalline anatase nanosheets with thickness of 10 nm. The morphology was manipulated by simply adjusting the molar ratio of tetrabutyl titanate/P123. At a low molar ratio of 17.04, TiO₂ microspheres composed of a large number of nanosheets closely packed together were obtained. At a high molar ratio of 34.08, TiO₂ hybrid architectures with polycrystalline anatase hierarchical microspheres and single-crystal anatase mesoporous (approximately 5 nm) nanospheres were obtained. Investigations on evolution formation revealed that P123 played a key role in the formation of a well-defined hierarchical structure. The photocatalytic performances of the obtained samples were investigated by the degradation of methylene blue and papermaking wastewater. When compared with commercial P25, the obtained hierarchical TiO₂ microspheres exhibit superior photocatalytic activity, high degradation efficiency, and good reproducibility. The product with hybrid architectures exhibited the highest photocatalytic activity. The chemical oxygen demand and the chroma removal rate of papermaking wastewater achieved 85.5 and 100%, respectively, after 12 h of photodegradation.     

TiO<Subscript>2</Subscript>–SiO<Subscript>2</Subscript> composite nanoparticles containing hindered amine light stabilizers encapsulated by MMA–PMPM copolymers

TiO₂–SiO₂ composite nanoparticles containing hindered amine light stabilizers (HALSs) were prepared by encapsulation of commercially available TiO₂–SiO₂ nanoparticles using methyl methacrylate (MMA) and 1,2,2,6,6-pentamethyl-4-piperidyl methacrylate (PMPM) copolymers through mini-emulsion polymerization. The Fourier transform infrared spectral analysis (FTIR) showed that the hindered amine light stabilizer PMPM was incorporated into the TiO₂–SiO₂/P(MMA-co-PMPM) composite nanoparticles. The X-ray photoelectron spectroscopy analysis (XPS) showed that the surface of TiO₂–SiO₂ nanoparticles was enriched with HALS moieties. The formation of P(MMA-co-PMPM) random copolymers on the surface of TiO₂–SiO₂ nanoparticles was determined by differential scanning calorimetry (DSC), and the percentage of the chemically grafted P(MMA-co-PMPM) coverage on the TiO₂–SiO₂ nanoparticles surface was 40.9 wt% determined by thermogravimetric analysis (TGA), which revealed that the TiO₂–SiO₂ nanoparticles were successfully encapsulated by MMA–PMPM copolymers. Scanning electron microscopy analysis indicated that the TiO₂–SiO₂/P(MMA-co-PMPM) composite nanoparticles were mainly homogeneous spherical shape particles, with an average size of about 90 nm. Rhodamine B (Rh.B) photocatalytic degradation study revealed UV-shielding characteristics for TiO₂–SiO₂/P(MMA-co-PMPM) composite nanoparticles and showed a remarkable decrease in photocatalytic activity of TiO₂–SiO₂ nanoparticles. These results indicated that TiO₂–SiO₂/P(MMA-co-PMPM) composite nanoparticles may be promising light stabilizers with covalent functionalization of polymeric HALS, which has little photocatalytic activity, and can be introduced into the weathering-resistant polymer materials to improve their application properties.     

Synthesis, characterization and enhanced photocatalytic activity of TiO2/SiO2 nanocomposite in an aqueous solution and acrylic-based coatings

In this study, TiO₂/SiO₂ nanocomposites were synthesized via a sol-gel route by adding tetraethylorthosilicate (TEOS) to a solution containing different molar ratios of Degussa P25 TiO₂ nanoparticles. FTIR, TGA, EDAX and XRD techniques were used to characterize the modified nanoparticles. Photocatalytic activity of the nanoparticles in an aqueous solution and into the acrylic based coating was evaluated using colour coordinate data measurements, SEM analysis, gloss measurements and FTIR spectroscopy, in the presence of Rhodamine B (Rh.B) dyestuff, as a pollutant model, before and after exposure to the UVA (340 nm) irradiation and compared to their unmodified counterparts.The results showed that silica grafting effectively reduced the photocatalytic activity of the TiO₂ nanoparticles as evidenced by absorption spectra and colour changes of Rh.B aqueous solutions during the UVA irradiation. The results revealed the effectiveness of sol-gel route for preparation of TiO₂/SiO₂ nanocomposites. The optimum result was obtained with 1% molar ratio of TiO₂:TEOS. Addition of TiO₂/SiO₂ nanocomposites into the acrylic based coating revealed reduction of photo-degradation of Rh.B compared to untreated nanoparticles. Finally, inclusion of TEOS treated TiO₂ nanoparticles into the aqueous organic coatings, provides photocatalytic property and as a result, it can possibly be considered for self-cleaning coatings.     

Photocatalytic TiO2 films and membranes for the development of efficient wastewater treatment and reuse systems

In order to develop efficient photocatalytic TiO₂ films and membranes for application in water and wastewater treatment and reuse systems, there is a great need to tailor-design the structural properties of TiO₂ material and enhance its photocatalytic activity. Through a simple sol–gel route, employing self-assembled surfactant molecules as pore directing agents along with acetic acid-based sol–gel route, we have fabricated nanostructured crystalline TiO₂ thin films and TiO₂/Al₂O₃ composite membranes with simultaneous photocatalytic, disinfection, separation, and anti-biofouling properties. The highly porous TiO₂ material exhibited high specific surface area and porosity, narrow pore size distribution, homogeneity without cracks and pinholes, active anatase crystal phase, and small crystallite size. These TiO₂ materials were highly efficient in the decomposition of methylene blue dye and creatinine, destruction of biological toxins (microcystin-LR), and inactivation of pathogenic microorganisms (Escherichia coli). Moreover, the photocatalytic TiO₂ membranes exhibited not only high water permeability and sharp polyethylene glycol retention but also less adsorption fouling tendency. Here, we report results on the synthesis, characterization, and environmental application and implication of photocatalytic TiO₂ films and membranes.     

BiOCl and TiO2 deposited on exfoliated ZnCr-LDH to enhance visible-light photocatalytic decolorization of Rhodamine B

A series of novel TiO₂-BiOCl-ZnCr-Ex composites for use as photocatalysts were synthesized via a facile solvothermal process using an exfoliated ZnCr-LDH (ZnCr-Ex) and depositing BiOCl and TiO₂ sequentially on the surface of ZnCr-Ex. The composites were characterized by XRD, TEM, SEM-EDS and UV–vis diffuse reflectance spectroscopy. In these composites, the BiOCl nanosheets were deposited first on the surfaces of ZnCr-Ex and then the TiO₂ nanoparticles were dispersed on the surface of BiOCl-ZnCr-Ex material as were seen from SEM and TEM analyses. The photocatalytic degradation of Rhodamine B (RhB) indicated that the TiO₂-BiOCl-ZnCr-Ex composite showed much higher visible-light photocatalytic activity for degradation of RhB than TiO₂ alone, BiOCl alone or the BiOCl-ZnCr-Ex by itself. The possible mechanisms of photocatalytic activity were discussed. Moreover, the present composite photocatalysts exhibited satisfactory re-usability for at least three cycles. Because of the facile synthesis process, higher photocatalytic activity under visible light irradiation and satisfactory re-usability of these composites, they can be touted as potential catalysts for degradation of organic pollutants in wastewater treatment.     

Preparation and characterization of high-surface-area titanium dioxide by sol-gel process

One of the important ways to improve photocatalytic efficiency is to prepare catalyst with enhanced surface area. In this work, titanium dioxide (TiO₂) nanoparticles having enhanced surface area were synthesized under the interference of SiO₂. The mixed oxide, SiO₂-TiO₂ (10% mol% Si), was prepared by a sol-gel procedure using titanium tetra-n-butoxide as Ti-precursor. The commercial SiO₂ nanoparticles were added into the TiO₂ sols after hydrolysis. After condensation and calcination heat treatment, the SiO₂-TiO₂ nanoparticles were obtained. To achieve the purpose of obtaining the high-surface-area TiO₂, the SiO₂ was removed subsequently by aqueous NaOH solution. The TiO₂ products were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), electron spectroscopy for chemical analysis (ESCA), and by N₂ adsorption-desorption isotherm. A fine mesoporous structure was formed for as-prepared TiO₂ after calcination at 400^°C and the average pore diameter was about 7 nm. The porous TiO₂ products possess mixing phases of anatase and rutile. Phase transformation from anatase to rutile occurred when the samples were calcined. The phase transition temperature is sensitive to the silicon content. The particle size of ～43 nm remained constant upon calcinations from 500 to 700^°C. The specific surface area was increased up to 66% compared to regular TiO₂ samples that were prepared by the similar sol-gel procedure. The porous TiO₂ nanostructures exhibited enhanced photocatalytic performance to decompose methylene blue under UV irradiation.