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Synthesis, structural characterization and catalytic application of citrate-stabilized monometallic and bimetallic palladium@copper nanoparticles in microbial anti-activities

In this research work, copper (Cu), palladium (Pd) and their bimetallic palladium@ copper (Pd@Cu) nanoparticles were synthesized using trisodium citrate as a stabilizing agent using the known chemical reduction method. The synthesized Cu, Pd and Pd@Cu nanoparticles were characterized by the ultravio...

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Bibliographic Details
Published in:International journal of nanomedicine 2017-01, Vol.12, p.8735-8747
Main Authors: Ullah, Inayat, Khan, Khakemin, Sohail, Muhammad, Ullah, Kifayat, Ullah, Anwar, Shaheen, Shabnum
Format: Article
Language:English
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Summary:In this research work, copper (Cu), palladium (Pd) and their bimetallic palladium@ copper (Pd@Cu) nanoparticles were synthesized using trisodium citrate as a stabilizing agent using the known chemical reduction method. The synthesized Cu, Pd and Pd@Cu nanoparticles were characterized by the ultraviolet-visible spectroscopy, scanning electron microscopy and X-ray diffraction spectroscopy, respectively. The different volumes of trisodium citrate were used for the stability of synthesized monometallic Cu, Pd and bimetallic Pd@Cu nanoparticles. The synthesized Cu, Pd and their bimetallic Pd@Cu nanoparticles were used as catalysts for the reduction of 4-nitrophenol in the presence of NaBH . The bimetallic Pd@Cu nanoparticles had efficient catalytic activities with a high rate constant (1.812 min ) as compared to monometallic Cu (0.3322 min ) and Pd (0.2689 min ) nanoparticles, respectively. The correlation coefficient ( 2) was found to be 0.99 for these three nanoparticles. Meanwhile, the effect of Cu, Pd and bimetallic Pd@Cu nanoparticles was checked on the physiology of specific different micro-organism strains. The bimetallic Pd@Cu nanoparticles reported the maximum resistance at maximum level the growth of bacterial strain and had observed a smooth antibacterial graph than the monometallic analogs.
ISSN:1178-2013
1176-9114
1178-2013
DOI:10.2147/IJN.S145085