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Co3O4 co-doped TiO2 nanoparticles were prepared by a low temperature thermal method and their functional relationships with metal ions was investigated using solid phase extraction. The analytical potential of Co3O4 co-doped TiO2 nanoparticles was studied for the selective extraction of lead using inductively coupled plasma-optical emission spectrometry. The selectivity of Co3O4 co-doped TiO2 nanoparticles was investigated toward different metal ions, including Cd(II), Co(II), Cr(III), Cu(II), Fe(II and III), Hg(II), La(III), Mn(II), Ni(II), Pb(II), Pd(II) and Y(III). Data obtained from the selectivity study showed that Co3O4 co-doped TiO2 nanoparticles have the highest selectivity toward Pb(II). The uptake capacity for Pb(II) was experimentally calculated to be 114.05 mg g−1. Moreover, adsorption isotherm data of Pb(II) on Co3O4 co-doped TiO2 nanoparticles fit well with the Langmuir adsorption isotherm, strongly supporting that the adsorption process was mainly as a monolayer on Co3O4 co-doped TiO2 nanoparticle surfaces.
Amorphous iron nanoparticles (Fe NPs) possess manifold applications in biomedical field owing to their unique physiochemical properties. Herein, a feasible green synthesis of Fe NPs is described employing choline chloride (ChCl) and sucrose (SR) based deep eutectic solvent (DES) as a stabilizing as well as capping agent. Stabilized Fe NPs were attained using precursors like ferric chloride hexahydrate (FeCl3.6H2O) and ferrous chloride tetrahydrate (FeCl2.4H2O) via co-precipitation method with potassium hydroxide (KOH) as a reducing agent. UV–Visible diffuse reflectance spectroscopy (UV-DRS) demonstrated characteristic broad absorption around 400–600 nm which illustrates the emergence of nanoparticles. Micrographs of the prepared material examined by electron microscopies (SEM, TEM), depicts spherical with size ranging from 80 to 180 nm. This was further reinforced with dynamic light scattering (DLS) technique. Low magnetization value demonstrated the superparamagnetic behaviour of the amorphous Iron nanoparticles which is notable for biomedical applications such as magnetic hyperthermia and localized drug delivery. Additionally; the characterized Fe NPs degrades rhodamine B (Rh B), a carcinogenic dye upto 96.06% within 30 min under UV light illumination, thus evidencing its usage by scientific community as suitable nanomaterial for dye removal from contaminated water samples. Antibacterial studies of the amorphous Fe NPs showed maximum zone of inhibition and activity index against waterborne pathogens Staphylococcus aureus, Micrococcus luteus, Proteus mirabilis, Klebsiella pneumonia and Escherichia coli. The obtained results showed that the Fe NPs are capable of inhibiting the growth of both Gram positive and Gram negative bacterial pathogens. Furthermore, cytotoxic effects of amorphous Fe NPs against HCT 116 and CCL 241 cancer cells exhibit dose dependent antiproliferation. The results proved that the amorphous Fe NPs can endure as a potential entrant for waste water management and treatment of cancer.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.