Degradation of Formaldehyde and Benzene by TiO2 Photocatalytic Cement Based Materials

A novel photocatalytic cement based material was prepared. The distribution of TiO2 on the surface of cement was characterized by scanning electron microscope（SEM） and X-ray diffraction（XRD）, which showed the relationship of photocatalysis and presence of TiO2. TiO2 also had an impact on cement hydration, which was studied by thermal analysis. With 300 W UV illuminations, formaldehyde and benzene were degraded efficiently by the prepared photocatalytic cement based materials. 15wt% TiO2/cement showed the highest degradation efficiency and capability. The results show that formaldehyde and benzene can be degraded within 4 and 9 hours, respectively. Besides, inorganic ions can induce TiO2 agglomeration. As a result, the presence of inorganic ions in cement is unfavorable for degradation. The photocatalytic cement based materials were fabricated and the degradation efficiency of formaldehyde was measured on building roof under sunlight illumination. Formaldehyde in glass chamber can be degraded thoroughly within 10 days.

Structural Characteristics and Photocatalytic Activity of Ambient Pressure Dried SiO2/TiO2 Aerogel Composites by One-step Solvent Exchange/Surface Modification

An ambient pressure synthesis of SiO2/TiO2 binary aerogel was prepared through the low-cost precursors of titanium tetrachloride（TiCl4） and sodium silicate（Na2O·nSiO2）.After gelation,solvent exchange and surface modification were performed simultaneously and the modified gel was finally dried under ambient pressure.Microstructural analyses by transmission electron microscope（TEM） indicate that fabricated SiO2/TiO2 aerogel composite shows similar sponge-like nanostructure as silica aerogel,and the Brunauer-EmmettTeller（BET） analysis shows that the specific surface area of the composite reaches 605 m^2/g,and the average pore size is 9.7 nm.Such binary aerogel exhibits significant photocatalytic performance in this paper for treating model pollutant of methyl orange（MO）,and the decolorizing efficiency of MO is detected as 84.9%after 210 mins exposure to UV light irradiation.Degraded gel suspends in the water so as to separate from solution for reuse,and after 4 times recycling,70%degradation efficiency can be easily reached when composite catalyzed system is exposed for 210 mins under UV irradiation.

Fabrication of WO3/TiO2 Heterostructures for Efficiently Photocatalytic Gaseous Hydrocarbons Degradation:Origin of Photoactivity and Revisit the Role of WO3 Decoration

Efficient oxidation of gaseous small molecular hydrocarbons under mild conditions remains a significant but challenging task to date. Here we report that WO3 decoration can obviously improve the performance of TiO2 （P25） toward the photocatalytic oxidation of several small molecular hydrocarbons （C2H6, C3H8 and C2H4） under simulated solar light irradiation. Among the WO3/TiO2 heterostructures, the 10wt%WO3/TiO2 nanocomposite shows the best photoactivities, which can efficiently oxidize C2H6, C3H8 and C2H4 within 15, 9 and 8 minutes, respectively under simulated sunlight with a light intensity of 200 mW/cm2. By strong contrast, a decreased photoactivity of TiO2 by coupling with WO3 is observed when investigating the performance of photocatalysts toward the degradation of methylene blue （MB） in liquid phase. The opposing effect of WO3 decoration on the performance of TiO2 is thoroughly investigated, and it is found that the improved photoactivities for gaseous hydrocarbon degradation is ascribed to the enhanced oxygen adsorption, resulting from WO3 decoration rather than efficient charge separation within the WO3/TiO2 heterostructures.

Tuning Effect of N_2 on Atmospheric-Pressure Cold Plasma CVD of TiO_2 Photocatalytic Films

To deposit TiO2 films through plasma CVD, the partial pressure ratio of O2 to TIC14 should be greater than the stoichiometric ratio （PO2/PTiCl4 〉 1）. However, this may lead to the formation of powder instead of film on the substrate when using volume dielectric barrier discharge （volume-DBD） at atmospheric pressure. In this study, by adding N2 into the working gas Ar, TiO2 photocatalytic films were successfully fabricated in the presence of excess O2 （PO2/PTiC14 = 2.6） by using a wire-to-plate atmospheric-pressure volume-DBD. The tuning effect of N2 on the deposition of TiO2 film was studied in detail. The results showed that by increasing the N2 content, the deposition rate and particle size of the TiO2 film were reduced, and its photocatalytic activity was enhanced. The tuning mechanism of N2 is further discussed.

Grain Size and Wettability of TiO_2/SiO_2 Photocatalytic Composite Thin Filing

The uniform transparent TiO2/SiO2 photocatalytic composite thin films are prepared by sol-gel method on the soda lime glass substrates, and characterized by UV-visible spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), BET surface area, FTIR spectroscopy and X-ray photoelectron spectroscopy (XPS). It was found that the addition of SiO2 to TiO2 thin films can suppress the grain growth of TiO2 crystal, increase the hydroxyl content on the surface of TiO2 films, lower the contact angle for water on TiO, films and enhance the hydrophilic property of TiO2 films. The super-hydrophilic TiO2/SiO2 photocatalytic composite thin films with the contact angle of 0((o) under bar) are obtained by the addition of 10%-20% SiO2 in mole fraction.

Enhanced Photoelectric Property of Mo-C Codoped TiO2 Films Deposited by RF Magnetron Cosputtering

Mo-C codoped TiO2 films were prepared by RF magnetron cosputtering. Ultraviolet-visible spectroscopy, atomic force microscopy, X-ray photoelectron spectroscopy, energy dispersive X-ray Analysis and X-Ray Diffraction were used to study the influences of codoping on energy gap, surface morphology, valence states of elements, ions content and crystal structure, respectively. The concentration of photogenerated carriers was measured by studying photocurrent density, while catalytic property was evaluated by observing degradation rate of methylene blue under visible light. A Mo-doped TiO2 film, whose content of Mo had been optimized in advance, was prepared and later used for subsequent comparisons with codoped samples. The result indicates that Mo-C codoping could curtail the energy gap and shift the absorption edge toward visible range. Under the illumination of visible light, codoped TiO2 films give rise to stronger photocurrent due to smaller band gaps. It is also found that Mo, C codoping results in a porous surface, whose area declines gradually with increasing carbon content. Carbon and Molybdenum doses were delicately optimized. Under the illumination of visible light, sample doped with 9.78at% carbon and 0.36at% Mo presents the strongest photocurrent which is about 8 times larger than undoped TiO2 films, and about 6 times larger than samples doped with Mo only.

Photocatalytic oxidation of nitric oxide from simulated flue gas by wet scrubbing using ultraviolet/TiO_2/H_2O_2 process

Nitric oxide(NO) from flue gas is hard to remove because of low solubility and reactivity. A new technology for photocatalytic oxidation of NO using ultraviolet(UV)/TiO2/H2O2 process is studied in an efficient laboratory-scale reactor. Effects of several key operational parameters on NO removal efficiency are studied, including TiO2 content, H2O2 initial concentration, UV lamp power, NO initial content, oxygen volume fraction and TiO2/H2O2 solution volume. The results illustrate that the NO removal efficiency increases with the increasing of H2O2 initial concentration or UV lamp power. Meanwhile, a lower NO initial content or a higher TiO2/H2O2 solution volume will result in higher NO removal efficiency. In addition, oxygen volume fraction has a little effect.The highest NO removal efficiency is achieved at the TiO2 content of 0.75 g/L, H2O2 initial concentration of 2.5 mol/L, UV lamp power of 36 W, NO initial content of 206×10-6 and TiO2/H2O2 solution volume of 600 m L. It is beneficial for the development and application of NO removal from coal-fired flue gas with UV/TiO2/H2O2 process.

Microstructural and photocatalytic characterization of cement-paste sol-gel synthesized titanium dioxide

ABSTRACT A routte for the in paste synthesis of TiO2 loaded cement is described. TiO2 sols are blended with fresh cement paste as an alternative process to add photocatalytic functionality to cement. The modification of cement paste structure after the addition ofTiO2 sols is analyzed by XRD, SEM and TGA. As a particular microstructural feature, TiO2 containing calcium silicate hydrate （C-H-S） particles are identified as networking centers ofa C-S-H gel fiber matrix. The increase of the TiO2 sol concentration induces a decrease of pore size and an increase in the specific surface area in the cement composites. The photocatalytic activity of the TiO2/cement system is evaluated from the degradation of Methylene Blue （MB） under UV irradiation, monitored through the absorbance at 665 nm. The results show that, although TiO2 phases reveal no long range order structure, the cement paste exothermal treatment in presence of hydrate products and alkaline conditions leads to a photocatalytic composite. Such new cement matrix may be twofold advantageous since it additionally promotes the formation of C-S-H gel, main determinant of cement mechanical properties.

Influence of supports on photocatalytic degradation of phenol and 4-chlorophenol in aqueous suspensions of titanium dioxide

The photocatalytic degradation of phenol and 4-chlorophenol （4-CP） in aqueous suspensions with the use of titanium dioxide （TiO2 ） under UV irradiation was examined. The effects of different supporting materials mixed physically with TiO2 were studied to achieve maximum degradation efficiency. Among the three supports, namely activated carbon （AC）, silica （SiO2 ） and zeolite （ZSM-5）, all exhibited paramount efficiency for degradation of phenol and 4-CP and was better than TiO2 alone. The optimum concentration was found to be 50 mg for all supporting materials. The efficiency order of the three supports was as follows： AC 〉 ZSM-5 〉 SiO2 , respectively. Whilst, the degradation of phenol and 4-CP was improved from 70.6% to 87.6% and 80.6% to 89.7%, respectively, within 120 min photocatalysis in the presence of optimal amount of AC. The degradation was also comparatively enhanced in the presence of cheaper rice husk and the activity was closed to ZSM-5 and lower than AC.

Surface modification of polypropylene non-woven fibers with TiO_2 nanoparticles via layer-by-layer self assembly method:Preparation and photocatalytic activity

Polypropylene（PP） meltblown fibers were coated with titanium dioxide（Ti O2） nanoparticles using layer-by-layer（Lb L） deposition technique. The fibers were first modified with 3layers of poly（4-styrenesulfonic acid）（PSS） and poly（diallyl-dimethylammonium chloride）（PDADMAC） to improve the anchoring of the Ti O2 nanoparticle clusters. PDADMAC, which is positively charged, was then used as counter polyelectrolyte in tandem with anionic Ti O2 nanoparticles to construct Ti O2/PDADMAC bilayer in the Lb L fashion. The number of deposited Ti O2/PDADMAC layers was varied from 1 to 7 bilayer, and could be used to adjust Ti O2 loading. The Lb L technique showed higher Ti O2 loading efficiency than the impregnation approach. The modified fibers were tested for their photocatalytic activity against a model dye, Methylene Blue（MB）. Results showed that the Ti O2 modified fibers exhibited excellent photocatalytic activity efficiency similar to that of Ti O2 powder dispersed in solution. The deposition of Ti O23 bilayer on the PP substrate was sufficient to produce nanocomposite fibers that could bleach the MB solution in less than 4 hr.Ti O2-Lb L constructions also preserved Ti O2 adhesion on substrate surface after 1 cycle of photocatalytic test. Successive photocatalytic test showed decline in MB reduction rate with loss of Ti O2 particles from the substrate outer surface. However, even in the third cycle, the Ti O2 modified fibers are still moderately effective as it could remove more than 95% of MB after 8 hr of treatment.

Photocatalytic parameters and kinetic study for degradation of dichlorophenol-indophenol (DCPIP) dye using highly active mesoporous TiO_2 nanoparticles

Highly active mesoporous TiO_2 of about 6 nm crystal size and 280.7 m^2/g specific surface areas has been successfully synthesized via controlled hydrolysis of titanium butoxide at acidic medium. It was characterized by means of XRD（X-ray diffraction）, SEM（scanning electron microscopy）, TEM（transmission electron microscopy）, FT-IR（Fourier transform infrared spectroscopy）, TGA（thermogravimetric analysis）, DSC（differential scanning calorimetry） and BET（Brunauer–Emmett–Teller） surface area. The degradation of dichlorophenol-indophenol（DCPIP） under ultraviolet（UV） light was studied to evaluate the photocatalytic activity of samples. The effects of different parameters and kinetics were investigated. Accordingly, a complete degradation of DCPIP dye was achieved by applying the optimal operational conditions of 1 g/L of catalyst, 10 mg/L of DCPIP, pH of 3 and the temperature at 25 ± 3°C after 3 min under UV irradiation. Meanwhile, the Langmuir–Hinshelwood kinetic model described the variations in pure photocatalytic branch in consistent with a first order power law model.The results proved that the prepared TiO_2 nanoparticle has a photocatalytic activity significantly better than Degussa P-25.

Reaction mechanism and metal ion transformation in photocatalytic ozonation of phenol and oxalic acid with Ag^+/TiO_2

Photocatalytic ozonation of phenol and oxalic acid （OA） was conducted with a Ag^＋/TiO2 catalyst and different pathways were found for the degradation of different compounds. Ag^＋ greatly promoted the photocatalytic degradation of contaminants due to its role as an electron scavenger. It also accelerated the removal rate of OA in ozonation and the simultaneous process for its complex reaction with oxalate. Phenol could be degraded both in direct ozonation and photolysis, but the TOC removal rates were much higher in the simultaneous processes due to the oxidation of hydroxyl radicals resulting from synergetic effects. The sequence of photo-illumination and ozone exposure in the combined process showed quite different effects in phenol degradation and TOC removal. The synergetic effects in different combined processes were found to be highly related to the properties of the target pollutants. The color change of the solution and TEM result confirmed that Ag＋ was easily reduced and deposited on the surface of Tit2 under photo-illumination, and dissolved again into solution in the presence of ozone. This simple cycle of enrichment and distribution of Ag^＋ can greatly benefit the design of advanced oxidation processes, in which the sequences of ozone and photo-illumination can be varied according to the needs for catalyst recycling and the different properties of pollutants.

Preparation of TiO2 microspheres with flower-like morphology through a water-in-oil emulsion route assisted by solvothermal treatment

Mesoporous TiO2 microspheres with flower-like morphology, high specific surface area, and high- crystallinity primary crystalline-phase of anatase have been prepared through a water-in-oil emulsion synthesis route assisted by solvothermal treatment. The as-prepared powder microspheres, as well as their precursor, were characterized by various techniques. Thermogravimetry and differential thermal analysis indicated that the optimal sintering temperature of the TiO2 precursor was 550 ℃. Field emission scanning electron microscopy, laser particle size analysis, and X-ray diffractionjointly confirmed that the precursor powder with a spherical structure and main particle sizes ranging from 3 to 20 μm had the same primary crystalline-phase as the TiO2 microspheres obtained from the calcination of the precur- sor at 550 ℃ for 4 h. The specific surface area of the TiO2 microspheres was approximately 123.6 m2/g according to the Brunauer-Emmett-Teller （BET） nitrogen adsorption results. Compared with the com- mercial TiO2 powder （P25）, the resulting TiO2 microspheres exhibited a higher photocatalytic activity. Based on the experimental results, a rational mechanism was proposed to elucidate the formation of the TiO2 microsoheres.

Review of the progress in preparing nano TiO_2: An important environmental engineering material

TiO2 nanomaterial is promising with its high potential and outstanding performance in photocatalytic environmental applications, such as CO2 conversion, water treatment, and air quality control. For many of these applications, the particle size, crystal structure and phase, porosity, and surface area influence the activity of TiO2 dramatically. TiO2 nanomaterials with special structures and morphologies, such as nanospheres, nanowires, nanotubes, nanorods, and nanoflowers are thus synthesized due to their desired characteristics. With an emphasis on the different morphologies of TiO2 and the influence factors in the synthesis, this review summarizes fourteen TiO2 preparation methods, such as the sol-gel method, solvothermal method, and reverse micelle method. The TiO2 formation mechanisms, the advantages and disadvantages of the preparation methods, and the photocatalytic environmental application examples are proposed as well.

TiO_2-loaded activated carbon fiber:Hydrothermal synthesis,adsorption properties and photo catalytic activity under visible light irradiation

TiO2-loaded activated carbon fibers （ACF） were prepared by a hydrothermal method. The samples were characterized by scanning electron microscopy （SEM）, X-ray diffraction （XRD）, Fourier transform infrared （FTIR） spectrometry and UV-vis diffuse reflectance spectra （DRS）. SEM images showed that the TiO2 nanoparticles were deposited on the surface of ACF, and the particle size and loading amount of TiO2 were varied by changing the initial concentration of tetrabutyl titanate （TBOT）. The results of an ash experiment showed that the loading amounts of TiO2 were 18.4%, 43.3%, 52.5%, 75.1%, and 91.1% for initial concentrations of TBOT of 0.07,014, 0.21,0.28, and 0.35 tool/L, respectively, Physical interactions played an important role in the formation of TiO2/ACF composite fibers that absorb UV and visible light. Compared with those of ACF, improved adsorption and photocatalytic activity toward Rhodamine B （RhB） were observed for TiO2/ACF composite fiber. The Rhodamine B could be removed efficiently by TiO2/ACF composite fibers, and the TiO2 loading amount had a significant effect on the photocatalytic activity of TiO2/ACF composite fibers.

Carbon nanotubes/TiO_2 nanotubes composite photocatalysts for efficient degradation of methyl orange dye

A series of carbon nanotubes/TiO2 nanotubes （CNTs/TNTs） composite photocatalysts were successfully prepared by incorporation of CNTs in HNO3 washing process. These photocatalysts were characterized by XRD, N2 physical adsorption, UV-vis diffuse reflectance spectroscopy, TEM and Raman spectroscopy, respectively, and their photocatalytic activities were tested by using methyl orange （MO） as a model compound. Also, the effects of amount of CNTs incorporated, calcination temperature and amount of catalyst on the photocatalytic activity of the composite photocatalyst were systematically investigated. The results show that the CNTs/TNTs composite exhibits much higher photocatalytic activity than that of the TNTs or CNTs alone.

In situ synthesis of CNTs/Fe-Ni/TiO_2 nanocomposite by fluidized bed chemical vapor deposition and the synergistic effect in photocatalysis

Carbon nanotube （CNTs）/Fe-Ni/TiO2 nanocomposite photocatalysts have been synthesized by an in situ fluidized bed chemical vapor deposition （FBCVD） method. The composite photocatalysts were characterized by XRD, Raman spectroscopy, BET, FESEM, TEM, UV-vis spectroscopy, and XPS. The results showed that the CNTs were grown in situ on the surface of TiO2. Fe（Ⅲ） in TiO2 showed no chemical changes in the growth of CNTs. Ni（Ⅱ） was partly reduced to metal Ni in the FBCVD process, and the metal Ni acted as a catalyst for the growth of CNTs. The photocatalytic activities of CNTs/Fe-Ni/TiO2 decreased with the rise of the FBCVD reaction temperature. For the sample synthesized at low FBCVD temperature （500 ℃）, more than 90% and nearly 50% of methylene blue were removed under UV irradiation in 180 min and under visible light irradiation in 300 min, respectively. The probable mechanism of synergistic enhancement of photocatalysis on the CNTs/Fe-Ni/TiO2 nanocomposite is proposed.

Fabrication of a superamphiphobic coating by a simple and flexible method

A facile and flexible method to prepare raspberry-like nanoparticles that can be used as a superamphipho- bic coating is reported. Anatase TiO2 nanoparticles were chosen as the core because of their irregular morphology and photocatalytic performance. Anatase TiO2 nanoparticles were surrounded tightly by tiny functional fluoride-silica nanoparticles via the hydrolysis-condensation reaction of tetraethoxysi- lane and IH, 1H, 2H, 2H-perfluorodecyl triethoxysilane. The obtained Si-F@TiO2 nanoparticles can be sprayed or dipped directly onto various substrates. The coated film exhibited quite good liquid resistance, even when subjected to water jetting and sand abrasion. The photocatalytic effect of the coated anatase TiO2 with respect to formaldehyde was also studied and discussed. This method will provide more opportunities and fast access to practical applications in surface, environmental, and energy engineering.