Preparation of Sn/Fe nanoparticles for Cr (III) detection in presence of leucine, photocatalytic and antibacterial activities.

In this project, Sn-Fe bimetallic nanoparticles were prepared by a facile method. The bimetallic nanoparticles of it could be well established by a field emission scanning electron microscope micrographs. Due to the excellent synergistic influence between Sn-Fe nanoparticles and leucine indicated a great performance for determination of Cr3+. The material was characterized using the XRD, DLS, and zetasizer for theevaluation of crystal structure and morphologyinformation.The potential and effective size of Sn-Fe NPs was -29.10 mV and 30 nm, respectively. Cr3+ ions interaction with the Sn-Fe NPs-leucine probe was carried out in 1 min as response time. The limit of detection of Sn-Fe NPs for Cr(III) colorimetric method was 0.25 nM. The prepared nanoparticles showed impressive photocatalysis efficiency for degradation of MO was about 95.1% in 35 min, thus the prepared nanoparticles may be developed for the detoxification of pollution. The prepared nanoparticles depicted effective antibacterial activity againstC. botulinum and, H. pylori bacteria.

Facile synthesis of gold-silver/copper sulfide nanoparticles for the selective/sensitive detection of chromium, photochemical and bactericidal application.

In this project, bimetallic Au-Agnanoparticles/CuS nanoparticles were prepared via simple hydrothermal methods, which were used as highly efficient material for Cr (III) detection, photocatalytic, and biological process. The Au-Ag/CuS nanoparticles was studied via UV-visible spectroscopy, field-emission scanning electron microscopy, Dynamic light scattering, and X-ray diffraction. The zeta potential and effective size of Au-Ag/CuS nanoparticles was -32.1 mV and 25 nm respectively. The response time of Cr (III) ions interaction was 2 min. The lowest detection of Cr (III) by Au-Ag/CuS nanoparticles was 0.5 nM. The Au-Ag/CuS nano catalyst was applied to decomposition of drug under visible lamp irradiation. The photo degradation response of drug was 100.0% in 30 min irradiation. The particles exhibited excellent antibacterial activities.

Application of response surface methodology to optimize the adsorption performance of a magnetic graphene oxide nanocomposite adsorbent for removal of methadone from the environment.

Magnetic graphene oxide (MGO) nanocomposites have been synthesized by the co-precipitation route. The surface structure of MGO nanocomposites were analyzed by XRD, TEM, SEM, VSM and nitrogen adsorption-desorption instrumental technique. Response surface methodology was used to optimize the removal of methadone by MGO nanocomposites in aqueous solution. Experiments were conducted based on Box-Behnken design (BBD). The influence of three parameters on the removal of methadone was examined using the response surface methodological approach. The significance of independent variables and their interactions were tested by analysis of variance (ANOVA). The optimum pH, adsorbent dose and temperature were found to be 6.2, 0.0098g and 295.7K, respectively. Under these conditions, removal efficiency of methadone was found to be 87.20mg/g.