Study on photocatalytic performance for hydrogen evolution over CdS/M-MCM-41 (M = Zr, Ti) composite photocatalysts under visible light illumination

A series of CdS/M(x)-MCM-41 (M = Zr, Ti, x stands for molar ratio of M/Si) photocatalysts were preprared by hydrotherm, ion-exchange and sulfidation process. The catalysts were characterized by X-ray diffraction, UV-vis spectra and N₂ adsorption-desorption isotherm et al. The characterization results shown that Zr or Ti was successfully doped into the mesoporous of MCM-41, and CdS was also successfully incorporated into such modified mesoporous. The results of photocatalytic performance for hydrogen production shown that CdS/Zr(0.005)-MCM-41 and CdS/Ti(0.02)-MCM-41 had the highest hydrogen evolution activity in triethanolamine aqueous solution under visible light (λ > 430 nm) irradiation, which can be explained by the diffusion velocity of the reactants and resultants and the protection which MCM-41 provided for CdS.     

Photocatalytic activity of Ag–TiO2-graphene ternary nanocomposites and application in hydrogen evolution by water splitting

TiO₂-graphene (P25-GR, PG) nanocomposite was fabricated with P25 and graphite oxide through a hydrothermal method, and then Ag nanoparticles (Ag NPs) was assembled in P25-GR (Ag-P25-GR, APG) under microwave-assisted chemical reduction. The prepared samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), transmission electron microscopy (TEM), photoluminescence spectrum (PL), UV–vis absorption spectrum (UV–vis) and Raman spectrum, respectively. The results showed that Ag NPs were well dispersed on the surface of PG with metallic state. The ternary Ag-P25-GR (APG) nanocomposites possessed the extended light absorption range and more efficient charge separation properties compared to binary P25-GR (PG). Methylene blue photodegradation experiment proved that surface plasmon resonance (SPR) phenomenon had an effect on photoreaction efficiency. The corresponding hydrogen evolution rate of APG prepared with 0.002 M AgNO₃ solution was 7.6 times than pure P25 and 2.7 times than PG in the test condition. The improved photocatalytic performance can be attributed to the presence of GR and SPR effect, leading to the longer lifetime of photo-generated electron–hole pairs and faster interfacial charge transfer rate. This work indicates that the photoactivity of ternary GR-based nanocomposites is superior to the binary one. We expected our work could give a new train of thought on exploration of GR-based nanocomposites.     

A comparative study of the effect of Pd-doping on the structural,optical, and photocatalytic properties of sol–gel derived anatase TiO2 nanoparticles

Pd-doped anatase TiO₂ nanoparticles were synthesized by a modified sol–gel deposition technique. The synthetic strategy is applicable to other transition and post-transition metals to obtain phase-pure anatase titania nanoparticles. This is important in the sense that anatase titania forms the most hydroxyl radicals (compared to other polymorphs like rutile, brookite, etc.) for better photocatalytic performance. XRD and Raman data confirm the phase-pure anatase formation. Doping of Pd²⁺ into Ti⁴⁺ sites (for substitutional doping) or interstitial sites (for interstitial doping) creates strain within the nanoparticles and is reflected in the XRD peak broadening and Raman peak shifts. This is because of the ionic radii difference between Ti⁴⁺(∼68 pm) and Pd²⁺(∼86 pm). XPS data confirm the formation of high surface titanol groups at the nanoparticle surface and a large number of loosely bound Ti³⁺–O bonds, both of which considerably enhance the photocatalytic activity of the doped nanoparticles. A comparative study with other metal doping (Ga) shows that TiO₂: Pd nanoparticles have more Ti³⁺–O bonds, which enhance the charge transfer rate and hence improve the photocatalytic activity compared to other transition and post-transition metal-doped titania nanostructures.     

One-dimensional spindle-like BiVO4/TiO2 nanofibers heterojunction nanocomposites with enhanced visible light photocatalytic activity

One-dimensional spindle-like BiVO₄/TiO₂ nanofibers heterojunction nanocomposites with high visible light photocatalytic activity have been successfully obtained by combining the electrospinning technique and solvothermal method. The as-obtained products were characterized by field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), UV–vis spectra and photoluminescence (PL) spectra. The results revealed that spindle-like BiVO₄ nanostructures were successfully grown on TiO₂ nanofibers. Photocatalytic tests showed that the BiVO₄/TiO₂ nanofibers heterojunction nanocomposites showed enhanced visible light photocatalytic activity than that of pure TiO₂ nanofibers, which might be attributed to the effective photogenerated electrons-holes separation based on the photosynergistic effect of the BiVO₄/TiO₂ heterojunction. Moreover, the BiVO₄/TiO₂ nanofibers heterojunction nanocomposites could be easily recycled without any decrease of the photocatalytic activity.     

Visible photocatalytic activity and photoelectrochemical behavior of TiO2 nanoparticles modified with metal porphyrins containing hydroxyl group

TiO₂ nanoparticles modified with 5-(p-hydroxylphenyl)-10,15,20-triphenylporphyrin (HTPP), 5-(p-hydroxylphenyl)-10,15,20-triphenylporphyrin zinc (ZnHTPP) and trans-dichloro-5-(p-hydroxylphenyl)-10,15,20-triphenylporphyrin tin (SnHTPP) were prepared in order to improve the visible photocatalytic activity of TiO₂ nanoparticles. The photocatalytic activity of the modified TiO₂ nanoparticles was investigated by carrying out the photodegradation of methyl orange in aqueous solution under visible light irradiation. The TiO₂ nanoparticles modified with SnHTPP show the highest visible photocatalytic activity with a degradation ratio of 86% of methyl orange after 180 min irradiation among three catalysts. This result indicates that the central metal ions in porphyrins can significantly influence the sensitization efficiency of porphyrins. In addition, the photoelectrochemical behavior of the modified TiO₂ nanoparticles was examined and related to their photocatalytic activity. Finally, the photocatalytic mechanism was discussed preliminarily.     

The dependence of the photocatalytic activity of TiO2/carbon nanotubes nanocomposites on the modification of the carbon nanotubes

Nanostructural TiO₂/modified multi-wall carbon nanotubes photocatalysts were prepared by hydrolysis of Ti(iso-OC₃H₇)₄ providing chemical bonding of anatase TiO₂ nanoparticles onto oxidized- or amino-functionalized multi-wall carbon nanotubes (MWCNT). The processes of functionalization of the MWCNT and the deposition of TiO₂ influence the photocatalytic activity of the synthesized nanocomposites. The phase composition, crystallite size, and the structural and surface properties of the obtained TiO₂/modified-MWCNT nanocomposite were analyzed from XRD, FEG-SEM, TEM/HRTEM and FTIR data, as well low temperature N₂ adsorption. In the photocatalytic study, the TiO₂/oxidized-MWCNT catalyst showed the highest and the TiO₂/amino functionalized-MWCNT catalysts somewhat lower degradation rates, indicating that the enhancement of photocatalysis was supported by the more effective electron transfer properties of the oxygen- than amino-containing functional groups, which support the efficient charge transportation and separation of the photogenerated electron-hole pairs.     

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.     

Synthesis of ternary zinc spinel oxides and their application in the photodegradation of organic pollutant

Ternary zinc spinel oxides such as Zn₂SnO₄, ZnAl₂O₄ and ZnFe₂O₄ were synthesized and characterized, and their activities in the photodegradation of phenol molecules were investigated. Zn₂SnO₄, ZnAl₂O₄ and ZnFe₂O₄ powders were synthesized by hydrothermal, metal–chitosan complexation and solvothermal routes, respectively. The face-centered cubic spinel structure of each material was confirmed by powder X-ray diffractometry (XRD) and its porous structure by N₂ adsorption–desorption isotherms. The characterization of spinels was complemented with Fourier transform infrared spectroscopy (FTIR) and X-rays fluorescence (XRF), revealing the formation of spinel structures with high purity. The photocatalytic activity in the degradation of phenol was observed only with Zn₂SnO₄ oxide. Mineralization degree of phenol molecules by Zn₂SnO₄ photocatalyst determined by total organic carbon analysis (TOC) reached 80% at 360 min under sunlight.     

A Review of Dehydration of Various Industrial Sludges

Wastewater characteristics and sludge generation potential of point source categories are reviewed critically. Novel industry-specific sludge dewatering/drying solutions necessary to establish a sustainable model are examined through a detailed literature survey. Knowledge of sludge properties is one of the most critical issues needed to design dewatering/drying equipment. This study focuses on industrial wastewater/sludge characterization. In addition, a comprehensive review of current drying models and technologies is also presented. A summary of the results derived from a novel thin-film-based photonic sludge dewatering/drying study is outlined as an alternative approach for industrial sludge control. Sludge was dried in a tubular quartz reactor (TQR), the inner surface of which was coated with a TiO₂ thin film. The TQR was irradiated with UV A, UV B, and UV C lamps. The consumed and generated energy fluxes through endergonic and exergonic reactions driven by photolysis and photocatalysis were investigated. In addition, the variations in sludge dewatering/drying characteristics were also examined and compared with conventional methods to evaluate the energy requirements.