Preparation of aerochitin‐TiO2 composite for efficient photocatalytic degradation of methylene blue

An aerochitin–titania (TiO₂) composite was successfully synthesized and characterized by Fourier transform infrared spectroscopy, X‐ray diffraction, thermogravimetric analysis, field emission scanning electron microscopy, and N₂ adsorption isotherms. The photocatalytic activity of the composite was investigated on the degradation of the model organic pollutant, methylene blue (MB) dye, under UV irradiation. The aerochitin–TiO₂ composite showed excellent adsorptive and photocatalytic activity with a degradation degree of 98% for MB. The first‐order rate constants for the photodegradation MB by TiO₂ nanoparticles and aerochitin–TiO₂ composite were found to be (3.49 ± 0.04) × 10^?3 and (1.82 ± 0.02) × 10^?2 min^?1. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45908.     

Ceramic tiles coated with Zr-Ag co-doped TiO2 thin film for indoor air purifying and antimicrobial applications

In this study, Zr-Ag co-doped TiO₂ (ZAT) photocatalyst films having varied numbers of layers (1, 2, 3, and 4) have been developed to coat on ceramic tile substrates by sol-gel spin coating technique. The specimens were tested to determine antibacterial activity against Escherichia coli and the capability to degrade gaseous formaldehyde under visible light. X-ray diffraction, ultraviolet and visible absorption spectroscopy, water contact angle, and scanning electron microscopy were applied to characterize the structural and morphological properties of the samples. The photocatalytic reactivity of the nanocomposite films was investigated by the decolorization of methylene blue (MB) dye under visible light irradiation. The results showed that the two-layer ZAT photocatalyst film on ceramic tile exhibited the highest photocatalytic decolorization of MB, with 60.36% efficiency. The ZAT tile had formaldehyde degradation efficiency up to 32.74% within only 6 h under visible light irradiation, higher than that of the bare ceramic tile (4.90%). Additionally, the ZAT thin films could enhance anti-E. coli activity and could be capable of degrading air pollution.     

Water vapor permeability of the polyurethane/TiO2 nanohybrid membrane with temperature sensitivity

A novel thermal‐sensitive polyurethane (TSPU)/TiO₂ nanohybrid membrane was successfully prepared via in situ process and used for controllable water vapor permeation. Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and differential scanning calorimetry (DSC) were employed to reveal the nanohybrid mechanism between TSPU and TiO₂ and the thermal sensitive characteristics of TSPU/TiO₂ nanohybrid membranes. FTIR analysis demonstrates that the highly active nano‐TiO₂ particles produced by the hydrolysis of the nanoprecursor (tetrabutyl titanate) have reacted with the active groups of TSPU. And some new peaks assigned to the Ti? O? C, Ti? C, and Ti? O? Ti bonds occur in the FTIR spectra of TSPU/TiO₂ nanohybrid membrane; these chemical bonds are believed to contribute to the higher mechanical properties of nanohybrid samples. DSC study indicates that nanohybridization does not disrupt the intrinsic phase‐separated structures and thermal‐sensitive characteristics of pure TSPU, the difference in behavior is the phase transition temperature (defined as switch temperature, T_s) of the reversible phase shifting from 50.1 to 53.4°C. SEM analysis shows that the nano‐TiO₂ particles are evenly distributed in TSPU and the size of the nano‐TiO₂ is lower than 100 nm. In addition, the water vapor permeability (WVP) of nanohybrid membrane is found to depend on the TiO₂ content. To be specified, when TiO₂ content is lower than 5.0 wt %, the nanohybrid samples show lower WVP at low temperatures and higher WVP at high temperatures than pure TSPU. Especially, when the temperature exceeds the T_s, for example from 50 to 60°C, the WVP of pure TSPU show improvement by 114%, whereas the WVP of the nanohybrid TSPU with 5.0 wt % TiO₂ content shows improvement by 145%, the latter shows more sensitivity to thermal stimuli. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Synthesis and characterization of interpenetrating polymer network based on sodium alginate and methacrylic acid and potential application for immobilization of TiO2 nanoparticles

An interpenetrating polymer network (IPN) based on the sodium alginate (A) and partially neutralized poly(methacrylic acid) (MAA) was prepared by free radical polymerization followed by additional cross‐linking of sodium alginate with calcium ions. Obtained material (A/MAA IPN) was characterized by FTIR spectroscopy, thermogravimetric analysis, scanning electron microscopy, and rheological measurements. Swelling behavior of synthetized IPN has been also investigated. TiO₂ nanoparticles (TiO₂ NPs) were immobilized onto A/MAA IPN by dip‐coating method and obtained TiO₂/IPN nanocomposite was used for removal of the methylene blue (MB) from aqueous solution. The photodegradation (under illumination) and sorption (in the dark) processes for dye removal were monitored through decrease of dye concentration in the solution by UV/VIS spectrometer. The TiO₂/IPN nanocomposite sorbed approximately 93% of the MB from a 10 mg L^?1 MB solution in the dark, but no degradation occurred. Likewise, more than 93% of dye was removed after 8 h of illumination. However, after 24 h of illumination, the samples were discolored indicating that dye molecules were successfully degraded. Thus, the TiO₂/IPN nanocomposite could be utilized in the photodegradation–sorption process for the abatement of pollutants in water. POLYM. ENG. SCI., 55:2511–2518, 2015. © 2015 Society of Plastics Engineers     

Experimental analysis and optimization of the synthesizing property of nitrogen‐modified TiO2 visible‐light photocatalysts

BACKGROUND: The aim of this study was to investigate improvement of the photocatalytic activity of visible‐light driven nitrogen‐modified TiO₂ (N‐TiO₂) powder toward methyl blue (MB) and direct blue‐86 (DB‐86) dyes. The Taguchi method with an L₉ orthogonal array was applied to plan the synthesis parameters, i.e. nitrogen sources, nitrogen source concentrations, stirring time and calcined temperatures. 95% confirmation experiments were undertaken to verify the effectiveness of the Taguchi method. RESULTS: All N‐TiO₂ photocatalysts were shifted toward the visible light region with the optical band gap (Eg). Nitrogen source concentrations were significant parameters for the photocatalytic decolorization rate constants (k values). In comparison with pure TiO₂, the photodecolorization behavior of N‐TiO₂ toward DB‐86 was superior with a reaction rate constant of 1.68 × 10^?3 min^?1, and a 4 h photodecolorization efficiency of 34%. CONCLUSION: The Taguchi method was reported to alter the surface properties of commercial Degussa P25 TiO₂, which could then be used as a visible‐light driven photocatalyst. The visible‐light‐driven photocatalyst was investigated to determine material characteristics. Greater photodecolorization of MB and DB‐86 dye pollutants using optimally‐prepared N‐TiO₂ under visible light irradiation was successfully obtained. Copyright © 2011 Society of Chemical Industry     

Synthesis of TiO2−xNy/Ag‐PbMoO4 Composite and Their Photocatalytic Activity Under Simulated Solar Light Irradiation

TiO_2?xN_y/Ag‐PbMoO₄ composite were synthesized by sonochemical method. The results revealed that the band‐gap energy absorption edge of TiO_2?xN_y/Ag‐PbMoO₄ composite was shifted to a longer wavelength as compared to TiO₂, TiO_2?xN_y, PbMoO_4, and Ag‐PbMoO₄. The TiO_2?xN_y/Ag‐PbMoO₄ composite showed the enhanced photocatalytic activity for degradation of indigo carmine dye (ICD) under simulated solar light irradiation. The TiO_2?xN_y/Ag‐PbMoO₄ composite exhibited the highest percentage (95.4%) of degradation of ICD and the highest reaction rate constant (0.0244 min^?1) in 2 h. The results suggested that a good combination of Ag and TiO_2?xN_y nanoparticles has great influence on the photocatalytic behavior of PbMoO₄.     

Development of mesoporous titanium dioxide hybrid poly(vinylidene fluoride) ultrafiltration membranes with photocatalytic properties

A photocatalytic activity ultrafiltration membrane (UFM) was prepared by the blending of a poly(vinylidene fluoride) (PVDF) polymer with mesoporous titanium dioxide (M‐TiO₂) particles via the phase‐inversion method. The microstructure of the membrane and Ti element distribution were characterized by scanning electron microscopy and energy‐dispersive X‐ray spectroscopy. Their properties were also determined by thermogravimetric analysis, differential scanning calorimetry, Fourier transform infrared spectroscopy, tensile stress tests, contact angle tests, bovine serum albumin retention, water flux, and permeation flux. When the M‐TiO₂ concentration reached 1 wt %, the thermal stability, mechanical properties, hydrophilicity, flux, and antifouling performance of the M‐TiO₂/PVDF UFM were improved to an optimal value with the M‐TiO₂ particles successfully entrapped and evenly distributed throughout the PVDF polymer matrix. Compared with the P25‐modified PVDF UFM (1 wt %), the M‐TiO₂‐modified PVDF UFM (1 wt %) exhibited better photocatalytic activity and wonderful stability in the UV photocatalytic degradation of the organic dye Rhodamine B. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43427.     

Enhanced photocatalytic activity of highly transparent superhydrophilic doped TiO2 thin films for improving the self-cleaning property of solar panel covers

Undoped and metal doped nanocrystalline TiO₂ transparent thin films were synthesized on glass substrates via sol-gel/dip-coating method. TiO₂ thin film coatings can be applied to the surfaces of solar panels to impart self-cleaning properties to them. The structural and optical properties of few nanometer-thick films were characterized by XRD, SEM, CA, AFM, XPS, and UV–Vis spectrophotometry techniques. The stoichiometric TiO₂ films crystallized in anatase phase, with a particle size of ～100 nm, which were uniformly distributed on the surface. The prepared films with a roughness of ～1–5 nm, increased the hydrophilicity of the glass surface. Reducing the amount of Ti precursor (X) favored the improvement of film quality. To improve the photocatalytic activity of the TiO₂ thin film, it was doped with Ni, Cd, Mo, Bi and Sr metal ions. The effect of metal doping on the photocatalytic activity of the films was investigated using the degradation process of methylene blue (MB) dye as the model contaminant. Among the prepared coatings, the Sr–TiO₂ film showed the highest efficiency for MB degradation. It increased the dye degradation efficiency of the films under both UV and Vis lights. The kinetic investigations also showed that the degradation of MB by TiO₂ and M ? TiO₂ films obeyed the pseudo-first order kinetics.     

Preparation and characterization of a novel activated carbon‐supported N‐doped visible light response photocatalyst (TiO2−xNy/AC)

A photocatalyst, TiO_2?xN_y/AC (activated carbon (AC) supported N‐doped TiO₂), highly active in both the Vis and UV range, was prepared by calcination of the TiO₂ precursor prepared by acid‐catalyzed hydrolysis in an ammonia atmosphere. The powders were characterized by diffuse reflectance spectroscopy, scanning electron microscopy, X‐ray diffraction, N₂ adsorption, Fourier transform infrared spectroscopy and phenol degradation. The doped N in the TiO₂ crystal lattice creates an electron‐occupied intra‐band gap allowing electron‐hole pair generation under Vis irradiation (500–560 nm). The TiO_2?xN_y/AC exhibited high levels of activity and the same activity trends for phenol degradation under both Vis and UV irradiation: TiO_2?xN_y/AC calcined at 500 °C for 4 h exhibited the highest activity. The band‐gap level newly formed by doped N can act as a center for the photo‐generated holes and is beneficial for the UV activity enhancement. The performance of the prepared TiO_2?xN_y/AC photocatalyst revealed its practical potential in the field of solar photocatalytic degradation of aqueous contaminants. Copyright © 2007 Society of Chemical Industry     

Synthesis,physical properties,and characterization of starch‐based blend films by adding nano‐sized TiO2/poly(methyl metacrylate‐co‐acrylamide)

The purpose of this study was to improve the physical properties and to expand the application range of starch‐based blend films added nano‐sized TiO₂/poly(methyl methacrylate‐co‐acrylamide) (PMMA‐co‐AM). Starch‐based blend films were prepared by using corn starch, polyvinyl alcohol (PVA), nano‐sized PMMA‐co‐AM, nano‐sized TiO₂/PMMA‐co‐AM particles, and additives, i.e., glycerol (GL) and citric acid (CA). Nano‐sized PMMA‐co‐AM was synthesized by emulsion polymerization and TiO₂ nanoparticles were also prepared by using sol–gel method. Nano‐sized TiO₂/PMMA‐co‐AM particles were synthesized by wet milling for 48 h. The morphology and crystallinity of TiO₂, nano‐sized PMMA‐co‐AM and TiO₂/PMMA‐co‐AM particles were investigated by using the scanning electron microscope (SEM) and X‐ray diffractometer (XRD). In addition, the functional groups of the TiO₂/PMMA‐co‐AM particles were characterized by IR spectrophotometry (FTIR). The physical properties such as tensile strength (TS), elongation at break (%E), degree of swelling (DS), and solubility (S) of starch‐based films were evaluated. It was found that the adding of nano‐sized particles can greatly improve the physical properties of the prepared films. The photocatalytic degradability of starch/PVA/nano‐sized TiO₂/PMMA‐co‐AM composite films was evaluated using methylene blue (MB) and acetaldehyde (ATA) as photodegradation target under UV and visible light. The degree of decomposition (C/C₀) of MB and ATA for the films containing TiO₂ and CA was 0.506 and 0.088 under UV light irradiation and 0.586 (MB) and 0.631 (ATA) under visible light irradiation, respectively. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Sonocatalysis and Photocatalysis in Ba0.5Sr0.5TiO3 ceramics

The photocatalytic, sonocatalytic, and sono-photocatalytic performances of Ba_0.5Sr_0.5TiO₃ (BST) ceramic (synthesized through solid-state reaction route) were investigated for the degradation of an organic dye named methylene blue (MB). The as-prepared BST ceramic powder was characterized using a scanning electron microscope, X-ray diffraction, X-ray photoelectron, and Raman spectroscopy techniques. The optical energy band gap of BST ceramic was found to be ∼3.17 eV. BST has shown significant catalytic activity following sonocatalysis and photocatalysis processes, i.e, ∼48% and ∼65% in 3 h, respectively. The synergic effect of the sonocatalysis and photocatalysis processes had shown an excellent degradation of 81% in 3 h. To determine the reactive species responsible for the degradation of MB dye, a scavenger test was also performed using isopropyl alcohol (IPA), ethylenediaminetetraacetic acid (EDTA), and benzoquinone (BQ) scavengers. The degree of MB dye degradation was quantified by a phytotoxicity test on “Vigna radiata” seeds. Furthermore, the potentiality of BST ceramic was explored for water cleaning applications while irradiating it to solar radiation in real-time conditions.     

Rutile-TiO2: Post heat treatment and its influence on the photocatalytic degradation of MB dye

Photocatalytic degradation of hazardous Methylene blue (MB) attracts greater concern as it is the dominant effluent of textile industry that is mixing with the ground water resources. In this regard, we have explored the possibility for an efficient optimization of MB dye degradation using rutile TiO₂. We have studied the post heat treatment of faceted Rutile TiO₂ nano crystallites synthesized by sol-gel method, which was carried out towards understanding the generation of surface states and its role on the dye degradation. The phase purity and its morphological structures were confirmed by XRD, Raman analysis, FESEM and HRTEM. The XPS analysis reveals the passivation of Ti³⁺ defect upon high temperature treatment above 600 ?C and also found generating surface defect states which are evidenced from the photoluminescence study. An EPR investigation clearly reveals the distributed presence of electron and hole trap states in the faceted R–TiO₂ nano crystallites. Corresponding EIS measurement of flat band potential of the electrochemical interface between R–TiO₂/NaCl shows the upward band bending of R–TiO₂ favourable for the improved charge transfer between R–TiO₂ to Methylene blue (MB) dye. The consolidated results indicate that the high temperature treatment passivates the Ti³⁺ defects and promotes the generation of surface defects that favourably enhances the photocatalytic performance of MB dye from 63% to 90%. The details are discussed in this paper.     

The Assembly of TiO2 Nanoparticles into Micrometer‐Sized Structures,Photocatalytically Active Under UV and Vis Light

Micrometer‐sized structures consisting of TiO₂ nanoparticles were prepared using the sol–gel technique in combination with the structure‐directing agent triethanolamine (TEA). The interaction of the TEA with the hydrolyzed sol–gel products led to the formation of TEA titanate complexes, which then enabled the assembly of sol–gel‐precipitated nanosized powders. A subsequent thermal treatment of these powders resulted in the formation of micrometer‐sized structures consisting of TiO₂ anatase and rutile nanoparticles. To characterize the prepared powders, FTIR spectroscopy, XRD analysis, the Brunauer‐Emmett‐Teller method (s_BET), UV–Vis spectrometry and electron microscopy (FE‐SEM, and TEM) were employed. The photocatalytic degradation of the azo dye known as methylene blue was monitored under UV and Vis irradiation and showed that the micrometer‐sized structures consisting of TiO₂ nanoparticles exhibited a similar photocatalytic activity to submicrometer‐sized structures consisting of TiO₂ nanoparticles prepared without TEA.     

Synthesis of Octa(maleimidophenyl) silsesquioxane–SiO2/TiO2 Hybrid Nanocomposites: Adsorption Behavior for the Removal of an Organic Methylene Blue Dye and Antimicrobial Activity against Pathogens

In this study, a sol–gel process was used to prepare hybrid nanocomposite consisting of octa(maleimidophenyl) silsesquioxane-silica/titania (maleimide–POSS (polyhedral oligomeric silsesquioxanes)–SiO₂/TiO₂) to use in methylene blue (MB) adsorption and as an antibacterial agent. The structure, surface, and morphological characteristics were confirmed through Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and transmission electron microscopy. The optical and thermal stabilities were studied by conducting UV–visible and thermogravimetric analysis–differential scanning electron calorimetry analysis. The experimental results showed a maximum dye adsorption capacity of 92% achieved using 0.5?g of hybrid nanocomposite after 2.5?h at pH 9. We also investigated the effect that the adsorbent dosage, pH, and contact time had on the removal efficiency of the MB dye in aqueous solution. The recycling experiment showed a good adsorption capacity of the MB dye, even after five repeated cycles. Furthermore, the hybrid nanocomposite was tested against pathogenic bacteria, such as Bacillus cereus, Lactobacillus, Escherichia coli, and Pseudomonas aeruginosa. The nanocomposite was observed to be highly sensitive to E. coli, B. cereus, and P. aeruginosa, as confirmed by the size of the zone inhibition.     

Preparation of nano‐TiO2/polystyrene hybride microspheres and their antibacterial properties

This study provided a facile method to prepare nano‐TiO₂/polystyrene hybride microspheres in ethanol solution. The formation of titanium dioxide (TiO₂) nanoparticles and hybrid microspheres were verified by FTIR, SEM, transmission electron microscopy, thermogravimetric analysis, and X‐ray powder diffraction. Monodispersed colloid TiO₂ nanoparticles with small particle sizes were obtained, and the average particle size could be effectively controlled from about 10 nm. The antibacterial activity of the organic microspheres and hybride microspheres was also investigated against Escherichia coli. They were able to efficiently inhibit the growth and the multiplication of E. coli under the UV. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Photodegradation of methylene blue with a titanium dioxide/polyacrylamide photocatalyst under sunlight

Hydrogels containing TiO₂ nanoparticles (NPs) have photocatalytic properties and degrade pollutants under light. In this study, a polyacrylamide (PAAm) hydrogel was synthesized with TiO₂ P25 NPs as the initiator, acrylamide as a monomer, and N,N′‐methylene bisacrylamide as a crosslinker in aqueous media under sunlight. Fourier transform infrared spectroscopy, thermogravimetric analysis, scanning electron microscopy, and transmission electron microscopy were applied to characterize the TiO₂/PAAm hydrogel. The effects of different synthetic conditions, such as the initiator concentration, crosslinker, and dilution, on swelling were investigated. The maximum swelling of the TiO₂/PAAm hydrogel was 45 g/g in the hydrogel synthesized with optimum conditions by 0.2% TiO₂. The photocatalytic degradability of the hydrogel was investigated with methylene blue (MB) as the pollutant target. Also, the effects of the pH and MB concentration were studied. Under optimum conditions, 95.00% of the MB was degraded by the TiO₂/PAAm photocatalyst after 5 h of irradiation under sunlight. The comparison of the results with those of the TiO₂ P25 powder showed that the TiO₂ NPs had better activity than the hydrogel, but unlike the hydrogel, the activity of these NPs decreased in each recycling time because of the aggregation of NPs. Finally, the hydrogel was recycled seven times without a considerable reduction in the degradation efficiency. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43386.     

Niobium‐Doped Titania Photocatalyst Film Prepared via a Nonaqueous Sol‐Gel Method

Niobium‐doped Titanium dioxide (Nb:TiO₂) transparent films were successfully deposited on glass substrates using a non‐aqueous sol‐gel spin coating technique. The effect of Nb concentration on the structural and photocatalytic properties of Nb:TiO₂ films was studied using X‐ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM), and UV visible spectroscopy. The films with 12 at.% (atomic percent) Nb doped TiO₂ showed excellent photocatalytic activity through 97.3% degradation of methylene blue (MB) after 2 h of UV irradiation.     

TiO<Subscript>2</Subscript>-mediated photoelectrochemical decoloration of methylene blue in the presence of peroxodisulfate

Nanosized TiO₂ films on stainless steel were prepared by electrophoretic deposition and characterized by X-ray diffraction analysis and photo-voltammetry. The decoloration of methylene blue (MB) dye was used as a test reaction for the evaluation of photoelectrocatalytic activity of the prepared TiO₂ coatings. The influence of applied potential and potassium peroxodisulfate on the rate of MB decoloration was investigated. The possible mechanisms of MB oxidation under various experimental conditions are discussed.     

Photoelectric catalytic degradation of methylene blue by C60-modified TiO2 nanotube array

Fullerene (C₆₀)-modified TiO₂ nanotube array (TNA) was prepared by the electrophoresis deposition technique. The as-prepared samples showed the high efficiency for the photoelectric catalytic (PEC) degradation of nonbiodegradable azodyes methylene blue (MB). The highest PEC activity of C₆₀-modified TNA (TNA/C₆₀) was achieved at a lower bias potential (4.0 V), which was 2.3 times of the highest activity of TNA at 5.0 V. The high PEC activity came from the synergetic effect between C₆₀ and TiO₂, which promoted the charge separation, influenced the charge distribution of the electrical double layer and reduced the impedances of the Helemholtz and depletion layers. Moreover, the oxidation of MB was a quick process during the PEC degradation, and the process began with the oxidation of the dimethylamino group, which was different from the photocatalytic (PC) process began with the oxidation of S atom; MB was mineralized completely during PEC degradation.     

Superhydrophilic Cu-doped TiO2 thin film for solar-driven photocatalysis

Nanosized Cu-doped TiO₂ film was prepared by the sol–gel spin coating technique. XPS analysis showed that Cu atoms had been successfully doped into TiO₂ lattice, which hence modified the surface chemical composition. As a result, the Cu-doped TiO₂ thin film possessed a superhydrophilic surface with a water contact angle (WCA) only 5.1° and exhibited excellent anti-fogging behavior. The Cu-doped TiO₂ thin film also exhibited a much better photocatalytic activity than the reference TiO₂ thin film, as evaluated by the degradation of 10 mg/L methylene blue (MB) solution under simulated solar-driven irradiation.