Farah Kanwal

Effect of crosslinker feed content on catalaytic activity of silver nanoparticles fabricated in multiresponsive microgels

We investigated the effect of crosslinking density of poly(N-isopropyl acrylamide-co-acrylic acid) microgels on catalytic activity of silver nanoparticles fabricated hybrid microgels. Multiresponsive poly(N-isopropyl acrylamide-co-acrylic acid) microgels with 2, 4, 6 and 8 mole percentage of N,N-methylene-bis-acrylamide were synthesized by emulsion polymerization. These microgels were characterized by dynamic light scattering and were used as microreactors to synthesize silver nanoparticles. Hybrid system was characterized by ultraviolet-visible spectroscopy. The catalytic activity of hybrid microgels with different crosslinker content was compared by studying the reduction of pnitrophenol as a model reaction. Kinetics of reaction was monitored by spectrophotometry. The value of the apparent rate constant decreases from 0.568 to 0.313min−1, when content of crosslinker are increased from 2 to 8 mole percentage respectively. This decreases in value of apparent rate constant is due to increase in diffusional barrier offered by high crosslinking of polymer network at high mole percentages of N,N-methylene-bis-acrylamide.

ISOTHERMAL AND THERMODYNAMICAL MODELING OF CHROMIUM (III) ADSORPTION BY COMPOSITES OF POLYANILINE WITH RICE HUSK AND SAW DUST

The adsorption of Cr (III) from water by polyaniline composites with rice husk and saw dust of Eucalyptus camaldulensis has been investigated in this study. The surface of adsorbents was characterized by FT-IR. Effect of various operational conditions like agitation time, initial pH, adsorbent dose, particle size of composites and temperature were studied in batch mode. The suitability of the data was confirmed by Langmuir and Freundlich isotherms. Thermodynamic studies showed that adsorption of Cr (III) on these composites occur spontaneously. Rice husk and saw dust modified the morphology of polyaniline by preventing its aggregation and improving its adsorption capacity.

Synthesis, characterization and fabrication of copper nanoparticles in N-isopropylacrylamide based co-polymer microgels for degradation of p-nitrophenol

Abstract 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.

Cobalt and nickel nanoparticles fabricated p(NIPAM-co-MAA) microgels for catalytic applications

Abstract In this research work, multi-responsive poly(N-isopropylacrylamide-co-methacrylic acid) copolymer microgels were synthesized via emulsion polymerization in aqueous medium. Then, nickel and cobalt nanoparticles were fabricated within these microgels by in situ reduction of metal ions using sodium borohydride (NaBH4) as a reducing agent. Fourier transform infrared spectroscopy was used to characterize these microgels. The pH sensitivity of these copolymer microgels was studied using dynamic light scattering technique (DLS). DLS studies revealed that the hydrodynamic radius of these microgels increased with the increase in pH of the medium at 25°C. The catalytic activity of hybrid microgels for the reduction of p-nitrophenol (4-NP) to p-aminophenol (4-AP) was investigated by UV-visible spectrophotometery. The value of apparent rate constant of reaction was found to change linearly with catalyst dosage. The nickel-based hybrid system was found to be five times more efficient as a catalyst compared to the cobalt-based hybrid system for the reduction of 4-NP to 4-AP in aqueous medium.

Removal of Chromium(III) Using Synthetic Polymers, Copolymers and their Sulfonated Derivatives as Adsorbents

This study is concerned with the development of some synthetic polymers, copolymers and their sulfonated derivatives as adsorbents. The effectiveness of these adsorbents in removing Cr(III) from aqueous solution was evaluated by batch technique. The influence of different experimental parameters on removal process such as solution pH, contact time, adsorbent dose, Cr(III) concentration and temperature were evaluated. Adsorption equilibrium was achieved in 20 to 30 min. at pH > 5. The Langmuir, Freundlich and Temkin adsorption isotherms were used to elucidate the observed sorption phenomena. The maximum Cr(III)37.8 mg/gram of PS(polystyrene) and 37.2 mg/g of SAN (styrene/acrylonitrile copolymer) was removed as evaluated from Langmuir isotherm while the heat of sorption was in the range 0.21–7.65 kJ/mol as evaluated from Temkin isotherm. It can be concluded that PS developed in this study exhibited considerable adsorption potential for application in removal of Cr(III) from aqueous media as compared to its copolymers and other derivatives used in this study.

High Dielectric Constant Study of TiO2-Polypyrrole Composites with Low Contents of Filler Prepared by In Situ Polymerization

TiO2/polypyrrole composites with high dielectric constant have been synthesized by in situ polymerization of pyrrole in an aqueous dispersion of low concentration of TiO2, in the presence of small amount of HCl. Structural, optical, surface morphological, and thermal properties of the composites were investigated by X-ray diffractometer, Fourier transform infrared spectroscopy, field-emission scanning electron microscopy, and thermogravimetric analysis, respectively. The data obtained from diffractometer and thermal gravimetric analysis confirmed the crystalline nature and thermal stability of the prepared composites. The dielectric constant of 5 wt% TiO2 increased with filler content up to 4.3 × 103 at 1 kHz and then decreased to 1.25 × 103 at 10 kHz.

Novel Method to Synthesize Highly Conducting Polyaniline/ Nickel Sulfide Nanocomposite Films and the Study of Their Structural, Magnetic, and Electrical Properties

In this paper, a systematical investigation on a novel, facile, and inexpensive single-step chemical route has been used for the preparation of highly conducting polyaniline/nickel sulfide (PANI/NiS) magnetic nanocomposite films at room temperature. First, the nickel sulfide nanoparticles with particle size in the range of 45-70 nm were synthesized using nickel chloride as a precursor, and then PANI nanocomposite films were prepared by dispersing different weight percentages of NiS (0%-5%) in the monomer using nebulizing technique with nitrogen gas as a driving force for monomer atomization. These novel grown films were then characterized for their microstructure, magnetic, and conducting properties by X-ray diffraction analysis, vibrating sample magnetometer, scanning electron microscopy, and two-point probe method. This technique has successfully resulted in good quality, highly conducting, ferromagnetic, uniform, well adherent, and porous nanostructure films.

Advancing Dielectric and Ferroelectric Properties of Piezoelectric Polymers by Combining Graphene and Ferroelectric Ceramic Additives for Energy Storage Applications

To address the limitations of piezoelectric polymers which have a low dielectric constant andto improve their dielectric and ferroelectric efficiency for energy storage applications, we designed and characterized a new hybrid composite that contains polyvinylidene fluoride as a dielectric polymer matrix combined with graphene platelets as a conductive and barium titanite as ceramic ferroelectric fillers. Different graphene/barium titanate/polyvinylidene fluoride nanocomposite films were synthesized by changing the concentration of graphene and barium titanate to explore the impact of each component and their potential synergetic effect on dielectric and ferroelectric properties of the composite. Results showed that with an increase in the barium titanate fraction, dielectric efficiency ofthe nanocomposite was improved. Among all synthesized nanocomposite films, graphene/barium titanate/polyvinylidene fluoride nanocomposite in the weight ratio of 0.15:0.5:1 exhibited thehighest dielectric constant of 199 at 40 Hz, i.e., 15 fold greater than that of neat polyvinylidene fluoride film at the same frequency, and possessed a low loss tangent of 0.6. However, AC conductivity and ferroelectric properties of graphene/barium titanate/polyvinylidene fluoride nanocomposite films were enhanced with an increase in the graphene weight fraction. Graphene/barium titanate/polyvinylidene fluoride nanocomposite films with a weight ratio of 0.2:0.1:1 possessed a high AC conductivity of 1.2 × 10−4 S/m at 40 Hz. While remanent polarization, coercive field, and loop area of the same sample were 0.9 μC/cm2, 9.78 kV/cm, and 24.5 μC/cm2·V, respectively. Our results showed that a combination of graphene and ferroelectric ceramic additives are an excellent approach to significantly advance the performance of dielectric and ferroelectric properties of piezoelectric polymers for broad applications including energy storage.