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EN
Poly(N-isopropylacrylamide-co-acrylic acid) [P(NIPAM-co-AAc)] microgels were synthesized by precipitation polymerization. Copper nanoparticles were successfully fabricated inside the microgels by in-situ reduction of copper ions in an aqueous medium. The microgels were characterized by Fourier Transform Infrared Spectroscopy (FT-IR) and Dynamic Light Scattering (DLS). Hydrodynamic radius of P(NIPAM-co-AAc) microgel particles increased with an increase in pH in aqueous medium at 25 °C. Copper-poly(N-isopropylacrylamide-co-acrylic acid) [Cu-P(NIPAM-co-AAc)] hybrid microgels were used as a catalyst for the reduction of 4-nitrophenol (4-NP). Effect of temperature, concentration of sodium borohydride (NaBH4) and catalyst dosage on the value of apparent rate constant (kapp) for catalytic reduction of 4-NP in the presence of Cu-P(NIPAM-co-AAc) hybrid microgels were investigated by UV-Vis spectrophotometry. It was found that the value of kapp for catalytic reduction of 4-NP in the presence of Cu-P(NIPAM-co-AAc) hybrid microgel catalyst increased with an increase in catalyst dosage, temperature and concentration of NaBH4 in aqueous medium. The results were discussed in terms of diffusion of reactants towards catalyst surface and swelling-deswelling of hybrid microgels.
EN
Pakistan Poly(N-isopropylacrylamide-co-methacrylic acid) microgels [p(NIPAM-co-MAAc)] were synthesized by precipitation polymerization of N-isopropylacrylamide and methacrylic acid in aqueous medium. These microgels were characterized by dynamic light scattering and Fourier transform infrared spectroscopy. These microgels were used as micro-reactors for in situ synthesis of copper nanoparticles using sodium borohydride (NaBH4) as reducing agent. The hybrid microgels were used as catalysts for the reduction of nitrobenzene in aqueous media. The reaction was performed with different concentrations of catalyst and reducing agent. A linear relationship was found between apparent rate constant (kapp) and amount of catalyst. When the amount of catalyst was increased from 0.13 to 0.76 mg/mL then kapp was increased from 0.03 to 0.14 min−1. Activation parameters were also determined by performing reaction at two different temperatures. The catalytic process has been discussed in terms of energy of activation, enthalpy of activation and entropy of activation. The synthesized particles were found to be stable even after 14 weeks and showed catalytic activity for the reduction of nitrobenzene.
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