Fabrication and synergistically enhanced photocatalytic activity of ternary kaolinite, TiO2, and Al2O3 (K65T30A5) nanocomposite for visible-light-induced degradation of methylene blue and remazol red dye.

The ternary photocatalyst ((Al2Si2O5 (OH)4/TiO2/Al2O3) composites (where w/w = 65, 30, and 5 wt%) denoted K65T30A5 were successfully synthesized and examined for their efficiency in removing cationic (Methylene Blue, MB) and anionic (Remazol Red, RR) dye from aqueous medium under visible-light irradiation. A series of nanocomposites with varied wt% of kaolinite, TiO2, and Al2O3 were prepared through sonication followed by calcination at 600 °C. X-ray diffraction (XRD) analysis confirmed the crystallinity of the synthesized materials and established their average crystal size to be 83.87 nm. The morphological structure, composite molecule, and surface properties of the resulting K65T30A5 were characterized using FTIR, FE-SEM, and EDS analyses to confirm the successful fabrication of the nanocomposite. FTIR and EDS elemental mapping analyses confirmed the presence of Al, Si, Ti, and O elements in the nanocomposites. The composites exhibited photocatalytic behaviour across the UV-visible spectra, with values varying from the ultraviolet to the visible region with a sharp increase in reflectance at 510 nm. Near-complete degradation of MB (97.66 %) was achieved within 90 min at pH 9 and a 10 mg/L dye concentration, while RR removal reached 90.66 % within 120 min at pH 3.5 and the same dye concentration under visible light irradiation. The catalyst exhibited robust stability, retaining its efficiency by removing 85.09 % of MB and 80.21 % of RR dye after three reuse cycles. The composite catalyst discussed in this study emerges as a promising material for straightforward fabrication techniques, featuring a high percentage of kaolinite and proving to be a cost-effective solution for large-scale water and wastewater treatment processes.

Highly Efficient Water Oxidation Photoanode Made of Surface Modified LaTiO2 N Particles.

An improved variation of highly active/durable O2 -evolving LaTiO2 N powder-based photoelectrode has been fabricated by pre-cleaning the powder with mild polysulfonic acid and by homogeneous deposition of CoOx co-catalyst aided by microwave annealing. The treatment in aqueous solution of poly(4-styrene sulfonic acid) results in removal of surface LaTiO2 N layers, forming fine pores in the crystallites. The CoOx co-catalyst by microwave deposition in Co(NH3 )6 Cl3 /ethylene glycol homogeneously covers the particle surface. The LaTiO2 N powder is fabricated into particle-transferred electrodes on Ti thin film supported on solid substrate. The modified LaTiO2 N grains on the electrode serve as a highly active O2 -evolving photoanode achieving 8.9 mA cm-2 of the photocurrent density at 1.23 V versus reversible hydrogen electrode (RHE) in 0.1 m NaOH (pH 13) under solar-simulator irradiation Airmass 1.5 Global (AM 1.5G). The activity has been much improved, compared with conventional LaTiO2 N treated in mineral acid or with CoOx deposited by impregnation. The new electrode also exhibits better durability in fixed-potential chronoamperometric tests under AM 1.5G irradiation.

A review on technologies and their usage in solid waste monitoring and management systems: Issues and challenges.

In the backdrop of prompt advancement, information and communication technology (ICT) has become an inevitable part to plan and design of modern solid waste management (SWM) systems. This study presents a critical review of the existing ICTs and their usage in SWM systems to unfold the issues and challenges towards using integrated technologies based system. To plan, monitor, collect and manage solid waste, the ICTs are divided into four categories such as spatial technologies, identification technologies, data acquisition technologies and data communication technologies. The ICT based SWM systems classified in this paper are based on the first three technologies while the forth one is employed by almost every systems. This review may guide the reader about the basics of available ICTs and their application in SWM to facilitate the search for planning and design of a sustainable new system.

Synergistic enhanced photocatalytic and photothermal activity of Au@TiO2 nanopellets against human epithelial carcinoma cells.

The photocatalytic and plasmonic photothermal cancer cell-killing activity of the metallic Au-capped TiO(2) (Au@TiO(2)) composite colloidal nanopellets has been investigated on HeLa cells under UV-visible (350-600 nm) light irradiation. The Au@TiO(2) composite nanopellets with the uniform Au-capped TiO(2) structure were successfully synthesized by simple reduction of HAuCl(4) on the surface of TiO(2) nanoparticles. The morphological structure and surface properties of Au@TiO(2) were characterized by using UV-visible absorption spectroscopy, TEM, SEM, XPS, EDX and XRD analyses. The formation of hydroxyl radicals (˙OH) was confirmed by photoluminescence (PL) spectra. The photocatalytic and photothermal cell-killing activity of the Au@TiO(2) nanopellets was found to vary with the molar ratio of Au to TiO(2). The direct involvement of the metal particles in mediating the electron transfer from the photoexcited TiO(2) under the band gap excitation is considered to carry out the efficient photocatalytic reaction on the cells. The plasmonic absorption spectra of Au@TiO(2) suspensions were also measured for the evaluation of photothermal cell killing. The charge separation, the interfacial charge-transfer and photothermal activity promoted the photocatalytic-photothermal cancer-cell killing more than TiO(2) alone. The cytotoxic effect of Au@TiO(2) nanopellets with low concentration of gold (TiO(2) : Au molar ratio > 1 : 1) was found to be 100%, whereas that of the commercial TiO(2) (P25) was ca. 50%. The comparative study of the cell viability using Au alone and TiO(2) alone revealed that the synergistic effect of photocatalytic hydroxyl radical formation and Au-plasmonic photothermal heat generation plays a vital role in the cancer cell killing. A plausible mechanism was also proposed for photocatalytic cancer cell killing based on the obtained results.

Plasmon-induced photothermal cell-killing effect of gold colloidal nanoparticles on epithelial carcinoma cells.

Gold colloidal nanoparticles were prepared by the liquid laser ablation of a gold metal plate in water and also by the citrate reduction of HAuCl(4).4H2O. The gold colloidal nanoparticles with the plasmonic band strongly absorb light, which is converted to the photothermal energy. This photothermal energy gives a cytotoxic effect on epithelial carcinoma cells. Interestingly, we found that the size and shape of the nanoparticles are changed by light during the photothermal process in vitro. The cervical carcinoma cell line (HeLa cell) was incubated with the colloidal gold nanoparticles and then exposed to continuous visible light at 400-600 nm with UV- and heat-cutoff filters. The distinct cell-killing effect was observed by this procedure. In the absence of the gold colloidal nanoparticles, only a small amount of cells were photothermally destroyed.