Bi2WO6 nanoparticles anchored on membrane by grafting via in-situ polymerization for the treatment of antibiotic and pesticides wastewater.

Antibiotics, natural organic matter, and pesticides are detected in the ecosystem's domestic water, surface water, and groundwater and are largely applied in pharmaceuticals and agriculture. Polymeric membranes are effectively remove the various pollutants in the water bodies, but fouling is one of the major limitations of commercial membranes. Herein, we modified the polymeric membrane surface with inorganic photocatalytic nanoparticles. In this work, the hydrothermal method is used for the synthesis of Bi2WO6 nanoparticles and as-synthesized nanoparticles grafted onto the various polymeric membranes, including polyetherimide (PEI), cellulose acetate (CA), polyvinylidene fluoride (PVDF), and polysulfone (PSF). The functional group studies confirmed the existence of nanoparticles and hydroxyl groups on the hybrid membrane. Further, finger-like voids, top-surface morphology, and roughness on the membrane surface were validated via Field Emission Scanning Electron Microscopy (FESEM) and Atomic force microscopy (AFM), respectively. The significant rejection of tetracycline, humic acid, and fulvic acid + atrazine was noted with the synthesized membranes in the following order: PVDF (81.1%, 78.8%, 80.6%) > CA (70.1%, 69.3%, 71.7%) > PSF (72.5%, 73.6%, 67.1%) > PEI (75.9%, 65.5%, 63.7%). The photodegradation efficiency of hybrid membranes against tetracycline, humic acid, and fulvic acid + atrazine was observed in the order: PEI (28.5%, 25.8%, 30.2%) < CA (46.5%, 42.4%, 40.5%) < PSF (46.9%, 37.7%, 44.7%) < PVDF (67.7%, 62.1%, 64.3%). These membranes exhibit an outstanding permeate flux recovery ratio to the neat membrane. Therefore, the grafting of Bi2WO6 nanoparticles creates a potential bonding with PVDF membranes than other polymeric membranes, thus exhibiting an outstanding rejection than hybrid and neat membranes.

Development of starch-gelatin complex microspheres as sustained release delivery system.

The starch was isolated from jackfruit seeds and evaluated for its preformulation properties, like tapped density, bulk density, and particle size. The fourier transform infrared (FTIR) analysis was done and compared with that of the commercially available starch which confirmed the properties. Using the various concentrations of jackfruit seed starch, the microspheres were prepared, combining with gelatin by ionotropic gelation technique. The developed microspheres were subjected to analysis of particle size, drug content, entrapment efficiency, and percentage yield. The spectral analysis confirmed the presence of drug and absence of interactions. Scanning electron microscope image showed that the particles were in spherical shape with a rough surface. The in vitro drug release in water for 12 hours proved to be in the range of 89 to 100%. The various kinetic models were applied using release data to confirm the mechanism of drug. It was concluded that the jackfruit starch-gelatin microspheres gave satisfactory results and met pharmacopieal limits.