RESUMEN
Easily accessible robust synthesis of metallic nanoparticles (NPs) and their colloidal stabilization via successive surface functionalization with desired molecules are crucial for catalytic applications. In this research, tannic acid (TA)-functionalized bismuth (Bi)-based novel NPs were prepared via a simple in situ aqueous reduction of Bi3+ ions for the catalytic reduction of azo groups. The synthesis, morphology, and structure of Bi/TANPs were confirmed through spectroscopic, electron microscopic and X-ray diffraction analyses. The Bi/TANPs comprise Bi, carbon, oxygen and sodium as building components and possess a high negative surface charge of -58 mV, colloidal dispersity, thermal stability and crystalline structure. The Bi/TANPs are almost spherical shaped with an average diameter of 33 nm. The surface of the catalyst is mesoporous with a high specific surface area of 267 m2 g-1. The designed Bi/TANPs exhibit pH-specific affinity for azo dye molecules and reduced azo moieties in the presence of aqueous NaBH4 without requiring any hydrogen gas supply. The catalytic reduction efficiencies of Bi/TANPs against methylene blue and Congo red are almost 100%. These reduction reactions are very fast owing to the presence of TA moieties on the catalyst surface, which facilitate direct electron transfer to azo groups, and follow a pseudo-first-order kinetic model. The catalyst is mechanically recyclable, and shows a minimal loss (<3%) of its initial efficiency until the fifth cycle. This study not only developed an efficient catalyst for the remediation of azo dye-contaminated water, but also offers novel insights into the synergistic effects of TA and glycerin on the reduction mechanism of aqueous Bi3+ ions and the concomitant colloidal stabilization of Bi NPs.
RESUMEN
Drug conjugated iron oxide magnetite (Fe3O4) nanoparticles are of great interest in the field of biomedicine. In this study, vancomycin (Van) conjugated magnetite (Fe3O4) nanoparticles were envisioned to capture and inhibit the growth of bacteria. Hydrophobic Fe3O4 nanoparticles were synthesized by using co-precipitation of ferrous (Fe2+) and ferric (Fe3+) ions following a surface modification step with oleic acid as stabilizers. Thereafter, a ligand exchange technique was employed to displace oleic acid with hydrophilic dopamine (DOPA) molecules which have a catechol group for anchoring to the iron oxide surface to prepare water dispersible nanoparticles. The surface of the resulting Fe3O4/DOPA nanoparticles contains amino (-NH2) groups that are conjugated with vancomycin via a coupling reaction between the -NH2 group of dopamine and the -COOH group of vancomycin. The prepared vancomycin conjugated Fe3O4/DOPA nanoparticles were named Fe3O4/DOPA/Van and exhibited a magnetic response to an external magnetic field due to the presence of magnetite Fe3O4 in the core. The Fe3O4/DOPA/Van nanoparticles showed bactericidal activity against both Gram positive Bacillus subtilis (B. subtilis) and Streptococcus and Gram-negative bacteria Escherichia coli (E. coli). Maximum inhibition zones of 22 mm, 19 mm and 18 mm were found against B. subtilis, Streptococcus and E. coli respectively. Most importantly, the vancomycin conjugated nanoparticles were effectively bound to the cell wall of the bacteria, promoting bacterial separation and growth inhibition. Therefore, the prepared Fe3O4/DOPA/Van nanoparticles can be promising for effective bacterial separation and killing in the dispersion media.