Photocatalytic degradation of VOCs from air stream using Mo:TiO2/GAC nanocomposites

Modification of TiO2 is one of the techniques used to enhance its photodegradation efficiency and to make it visible-light-active. In this study, Mo-doped TiO2 nanoparticles were synthesized using a fast sol-gel technique, and then coated on granular activated carbon (GAC) as both substrate and adsorbent to obtain Mo:TiO2/GAC composite. The fabricated composite was characterized using powder XRD, SEM, EDAX, FTIR, and BET analysis. Then the composite was applied to photodegrade volatile organic compounds (VOCs) under both UV and visible light irradiation. The characterization results showed high crystallinity and purity. Mo:TiO2/GAC composite had higher photodegradation efficiency compared with bare TiO2 and bare GAC. Moreover, studying operational parameters showed that the optimum condition for photodegradation efficiency of VOCs was at flowrate of 1 l/min, VOCs concentration of 20 ppm, and light intensity of 400 and 600 W/m2 for UV and visible light respectively. The results suggest that Mo:TiO2/GAC is a visible-light-active composite and can be acceptably used to decompose VOCs under visible light with adequate efficiency and without the generation of harmful by-products such as O3 as compared with UV.

One-Step Preparation of RGO/Fe3O4-Fevo4 Nanocomposites As Highly Effective Photocatalysts Under Natural Sunlight Illumination

The study used a one-step hydrothermal method to prepare Fe3O4-FeVO4 and xRGO/Fe3O4-FeVO4 nanocomposites. XRD, TEM, EDS, XPS, DRS, and PL techniques were used to examine the structurally and morphologically properties of the prepared samples. The XRD results appeared that the Fe3O4-FeVO4 has a triclinic crystal structure. Under hydrothermal treatment, (GO) was effectively reduced to (RGO) as illustrated by XRD and XPS results. UV-Vis analysis revealed that the addition of RGO enhanced the absorption in the visible region and narrowed the band gap energy. The photoactivities of the prepared samples were evaluated by degrading methylene blue (MB), phenol and brilliant green (BG) under sunlight illumination. As indicated by all the nanocomposites, photocatalytic activity was higher than the pure Fe3O4-FeVO4 photocatalyst, and the highest photodegradation efficiency of MB and phenol was shown by the 10%RGO/Fe3O4-FeVO4. In addition, the study examined the mineralization (TOC), photodegradation process, and photocatalytic reaction kinetics of MB and phenol.

GC/MS screening of buckthorn phytochemicals and their use to synthesize ZnO nanoparticles for photocatalytic degradation of malachite Green dye in water

Zinc oxide nanoparticles (ZnO NPs) were biosynthesized. According to GC/MS analysis, chalcone; the main phytochemical; is probably complexed with Zn ions that are then oxidized to ZnO NPs by atmospheric O2 during heating. The ZnO NPs were characterized by TG, FTIR, XRD, FESEM, TEM, eEDAX, and BET surface area analysis. Sphere-like ZnO NPs were formed with 11 nm mean crystallite size, 5.2 m2 g−1 surface area, and 0.02 cm3 g−1 total pore volume. The synthesized ZnO showed excellent photocatalytic degradation (96.5±0.24% in 1 hour at 25 °C) of malachite green (MG) in aqueous solutions under UV light at optimum conditions; pH 10, MG initial concentration of 20 mg L−1, and ZnO dose of 1.5 g L−1. Also, ZnO showed very good reusability (92.9± 0.2% after 5 runs). The experimental data obeyed pseudo-first-order kinetics (R2=0.92). The photocatalysis process is dependent on the following species in the order: OH. > electron/positive hole pairs > O2.−. Moreover, photodegradation efficiency decreased in the presence of CO32−, HCO3−, and Cl−, but increased in the presence of NO3−, and SO42− ions. Thus, the green synthesized ZnO NPs can be applied as an efficient photocatalyst for the removal of MG from aqueous media.

Synergistic effect of sorption and photocatalysis on the degree of dye removal in single and multicomponent systems on ZnO-SnO2

The paper presents the photodegradation process of one-, two- and three-component dye mixtures by ZnO-SnO2 nanoparticles. After 60 min of running the processes, the dye removal efficiencies of 76.44, 72.69, 62.43, 77.00 and 92.46% for MB, RB, TB, MO and YQ degradation, respectively, were obtained. For binary and ternary systems, dye removal efficiencies for all cases exceeded 70%. When the binary and ternary dye mixtures were tested, the photodegradation efficiencies of ZnO-SnO2 were similar to those of the single mixtures, indicating that this material could be used in industrial applications in the future. The focus of the study was to investigate the effect of sorption on photodegradation efficiency and the presence of both cationic and anionic dyes on their degradation efficiency under UV light. The significance of the effect of sorption on the degradation efficiency allowing the interaction of the catalyst with the dyes removed was confirmed. The main factor influencing sorption and consequently photocatalysis was the nature of the dye. It was confirmed that the positively charged ZnO-SnO2 surface effectively sorbs the dyes and causes their degradation.

Synthesis of Ag decorated TiO2 nanoneedles for photocatalytic degradation of methylene blue dye

Water pollution due to the discharge of industrial effluents such as dyes is a serious concern that requires a potential remedy. In this context, photocatalysis is a potent and ecofriendly strategy to degrade these toxic water effluents. In this study, a novel approach to prepare TiO2 nanoneedles decorated with Ag nanoparticles is reported. The sample was prepared using modified photodeposition and was annealed at 400 °C. The X-ray diffraction (XRD) revealed that TiO2 in anatase phase with the presence of Ag were prepared successfully. The corresponding crystalline size of TiO2 and Ag were 6.86 nm and 3.94 nm, respectively. The scanning electron microscopy (SEM) showed that the prepared TiO2 exhibited nanoneedles structure decorated with Ag nanoparticles. The prepared sample exhibited impressive photocatalytic performance toward degrading of 50 ppm Methyl Blue (MB) in the presence of UV irradiation. Using catalyst dose of 4 mg the photodegradation efficiency (PDE) reached to 98.7% after 50 min of UV irradiation. This improved photocatalytic activity is attributed to high catalytic activity and surface area of the synthesized Ag decorated TiO2 nanoneedles.

Synthesis and Characterization of Manganese-Modified Black TiO2 Nanoparticles and Their Performance Evaluation for the Photodegradation of Phenolic Compounds from Wastewater

The release of phenolic-contaminated treated palm oil mill effluent (TPOME) poses a severe threat to human and environmental health. In this work, manganese-modified black TiO2 (Mn-B-TiO2) was produced for the photodegradation of high concentrations of total phenolic compounds from TPOME. A modified glycerol-assisted technique was used to synthesize visible-light-sensitive black TiO2 nanoparticles (NPs), which were then calcined at 300 °C for 60 min for conversion to anatase crystalline phase. The black TiO2 was further modified with manganese by utilizing a wet impregnation technique. Visible light absorption, charge carrier separation, and electron–hole pair recombination suppression were all improved when the band structure of TiO2 was tuned by producing Ti3+ defect states. As a result of the enhanced optical and electrical characteristics of black TiO2 NPs, phenolic compounds were removed from TPOME at a rate of 48.17%, which is 2.6 times higher than P25 (18%). When Mn was added to black TiO2 NPs, the Ti ion in the TiO2 lattice was replaced by Mn, causing a large redshift of the optical absorption edges and enhanced photodegradation of phenolic compounds from TPOME. The photodegradation efficiency of phenolic compounds by Mn-B-TiO2 improved to 60.12% from 48.17% at 0.3 wt% Mn doping concentration. The removal efficiency of phenolic compounds from TPOME diminished when Mn doping exceeded the optimum threshold (0.3 wt%). According to the findings, Mn-modified black TiO2 NPs are the most effective, as they combine the advantages of both black TiO2 and Mn doping.

Bis(4-methylpiperidine-1-carbodithioato)-lead(II) and Bis(4-benzylpiperidine-1-carbodithioato)-lead(II) as Precursors for Lead Sulphide Nano Photocatalysts for the Degradation of Rhodamine B

Bis(4-methylpiperidine-1-carbodithioato)-lead(II) and bis(4-benzylpiperidine-1-carbodithioato)-lead(II) were prepared and their molecular structures elucidated using single crystal X-ray crystallography and spectroscopic techniques. The compounds were used as precursors for the preparation of lead sulphide nano photocatalysts for the degradation of rhodamine B. The single crystal structures of the lead(II) dithiocarbamate complexes show mononuclear lead(II) compounds in which each lead(II) ion coordinates two dithiocarbamato anions in a distorted tetrahedral geometry. The compounds were thermolyzed at 180 ℃ in hexadecylamine (HDA), octadecylamine (ODA), and trioctylphosphine oxide (TOPO) to prepare HDA, ODA, and TOPO capped lead sulphide (PbS) nanoparticles. Powder X-ray diffraction (pXRD) patterns of the lead sulphide nanoparticles were indexed to the rock cubic salt crystalline phase of lead sulphide. The lead sulphide nanoparticles were used as photocatalysts for the degradation of rhodamine B with ODA-PbS1 achieving photodegradation efficiency of 45.28% after 360 min. The photostability and reusability studies of the as-prepared PbS nanoparticles were studied in four consecutive cycles, showing that the percentage degradation efficiency decreased slightly by about 0.51–1.93%. The results show that the as-prepared PbS nanoparticles are relatively photostable with a slight loss of photodegradation activities as the reusability cycles progress.

Rhodamine B Photodegradation in Aqueous Solutions Containing Nitrogen Doped TiO2 and Carbon Nanotubes Composites

In this work, new results concerning the potential of mixtures based on nitrogen doped titanium dioxide (TiO2:N) and carbon nanotubes (CNTs) as possible catalyst candidates for the rhodamine B (RhB) UV photodegradation are reported. The RhB photodegradation was evaluated by UV–VIS absorption spectroscopy using samples of TiO2:N and CNTs of the type of single-walled carbon nanotubes (SWNTs), double-wall carbon nanotubes (DWNTs), multi-wall carbon nanotubes (MWNTs), and single-walled carbon nanotubes functionalized with carboxyl groups (SWNT-COOH) having various concentrations of CNTs. The best photocatalytic performance was obtained for sample containing TiO2:N and 2.5 wt.% SWNTs-COOH, when approx. 85% of dye removal was achieved after 300 min. of UV irradiation. The reaction kinetics of RhB aqueous solutions containing TiO2:N/CNT mixtures followed a complex first-order kinetic model. The TiO2:N/CNTs catalyst induced higher photodegradation efficiency of RhB than TiO2:N due to the presence of CNTs, which act as adsorbent and dispersing agent and capture the photogenerated electrons of TiO2:N hindering the electron–hole recombination.

Synthesis, Characterization and Photodegradation Studies of Copper Oxide–Graphene Nanocomposites

In this work, a simple hydrothermal method was employed to prepare a pristine sample of copper oxide (CuO) and three samples of copper oxide–graphene nanocomposites (CuO-xG) with x = 2.5, 5, and 10 mg of graphene. The synthesized samples were characterized using X-ray powder diffractometry (XRD), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), Fourier-transform infrared spectroscopy (FTIR) and ultraviolet–visible (UV-Vis) spectroscopy. The XRD patterns of CuO-xG nanocomposites exhibited the diffraction peaks related to the crystal planes of monoclinic CuO and hexagonal graphite. The surface morphology of the prepared samples was investigated using FESEM images. EDX analysis was used to investigate the chemical composition of the synthesized samples. FTIR spectroscopy identified the vibrational modes of the covalent bonds present in the samples. The allowed direct optical bandgap energy was calculated for all prepared samples using UV-Vis absorption spectra. The small bandgap of CuO-xG nanocomposites indicates their potential use as an effective photocatalyst in the presence of visible light. Photocatalytic activity of the samples was explored for the degradation of methylene blue (MB) dye contaminant under visible light irradiation. The results showed that the CuO-5G sample has the highest photodegradation efficiency (~56%).