Arjun Maity

Composite nanofibers prepared from metallic iron nanoparticles and polyaniline: High performance for water treatment applications

Presented here is a simple preparation of metallic iron nanoparticles, supported on polyaniline nanofibers at room temperature. The preparation is based on polymerization of interconnected nanofibers by rapid mixing of the aniline monomer with Fe(III) chloride as the oxidant, followed by reductive deposition of Fe(0) nanoparticles, using the polymerization by-products as the Fe precursor. The morphology and other physico-chemical properties of the resulting composite were characterized by scanning and transmission electron microscopy, Brunauer-Emmett-Teller method, X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and vibrating-sample magnetometry. The composite fibers were 80-150 nm in diameter and exhibited the expected ferromagnetic behavior. The composite rapidly and efficiently removed As(V), Cr(VI), and also Congo red dye, from aqueous solutions suggesting their usefulness for removal of toxic materials from wastewater. The composite fibers have high capacity for toxin removal: 42.37 mg/g of As(V), 434.78 mg/g of Cr(VI), and 243.9 mg/g of Congo red. The fibers are easily recovered from fluids by exploiting their ferromagnetic properties.

Single stage batch adsorber design for efficient Eosin yellow removal by polyaniline coated ligno-cellulose.

Polyaniline-coated lignin-based adsorbent (PLC) was synthesized and used for uptake of reactive dye eosin yellow (EY) from aqueous solution. The adsorption capability of the adsorbent was found to be more effective than the unmodified adsorbent (LC). In particular, the adsorption capability of the PLC was effective over a wider pH range. This could be owing to its higher point of zero charge, which is more favorable for the uptake of the anionic dye. Adsorption isotherm models suggested a monolayer adsorption was predominant. The mean free energy of adsorption (E(DR)) was found to have values between 8 and 16 kJ mol(-1) which suggests that an electrostatic mechanism of adsorption predominated over other underlying mechanisms. The adsorption process was also found to be spontaneous, with increasing negative free energy values observed at higher temperatures. Chemisorption process was supported by the changes in enthalpy above 40 kJ mol(-1) and by the results of desorption studies. This new adsorbent was also reusable and regenerable over four successive adsorption-desorption cycles. The single stage adsorber design revealed that PLC can be applicable as an effective biosorbent for the treatment of industrial effluents containing EY dye.

Sonocatalytic rapid degradation of Congo red dye from aqueous solution using magnetic Fe0/polyaniline nanofibers

Nano-sized magnetic Fe0/polyaniline (Fe0/PANI) nanofibers were used as an effective material for sonocatalytic degradation of organic anionic Congo red (CR) dye. Fe0/PANI, was synthesized via reductive deposition of nano-Fe0 onto the PANI nanofibers at room temperature. Prepared catalyst was characterized using HR-TEM, FE-SEM, XRD, FTIR instruments. The efficacy of catalyst in removing CR was assessed colorimetrically using UV-visible spectroscopy under different experimental conditions such as % of Fe0 loading into the composite material, solution pH, initial concentration of dye, catalyst dosage, temperature and ultrasonic power. The optimum conditions for sonocatalytic degradation of CR were obtained at catalyst concentrations=500mg.L-1, concentration of CR=200ppm, solution pH=neutral (7.0), temperature=30°C, % of Fe0 loading=30% and 500W ultrasonic power. The experimental results showed that ultrasonic process could remove 98% of Congo red within 30min with higher Qmax value (Qmax=446.4 at 25°C). The rate of degradation of CR dye was much faster in this ultrasonic technique rather than conventional adsorption process. The degradation efficiency declined with the addition of common inorganic salts (NaCl, Na2CO3, Na2SO4 and Na3PO4). The rate of degradation suppressed more with increasing salt concentration. Kinetic and isotherm studies indicated that the degradation of CR provides pseudo-second order rate kinetic and Langmuir isotherm model compared to all other models tested. The excellent high degradation capacity of Fe0/PANI under ultrasonic irradiation can be explained on the basis of the formation of active hydroxyl radicals (OH) and subsequently a series of free radical reactions.

Sorption isotherms, kinetic and optimization process of amino acid proline based polymer nanocomposite for the removal of selected textile dyes from industrial wastewater

In this article, adsorption and kinetic studies were carried out on three textile dyes, namely Reactive Blue 222 (RB 222), Reactive Red 195 (RR 195) and Reactive Yellow 145 (RY 145). The dyes studied in a mixture were adsorbed under various conditions onto PRO-BEN, a bentonite modified with a new cationic proline polymer (l-proline-epichlorohydrin polymer). The proline polymer was characterized by 1H NMR, Fourier transform infrared spectroscopy (FT-IR), dynamic light scattering (DLS) and TEM. The PRO-BEN composite was characterized by FT-IR, dynamic light scattering (DLS) (zeta potential), TEM imaging, SEM/EDX and X-ray photoelectron spectroscopy (characterize the binding energy). During adsorption studies, factors involving pH, temperature, the initial concentrations of the dyes and the quantity of PRO-BEN used during adsorption were established. The results revealed that the adsorption mechanism was categorized by the Langmuir type 1 isotherm. The adsorption data followed the pseudo-second order kinetic model. The intraparticle diffusion model indicated that adsorption did not only depend on the intraparticle diffusion of the dyes. The thermodynamic parameters verified that the adsorption process was spontaneous and exothermic. The Gibbs free energy values indicated that physisorption had occurred. Successful adsorption of dyes from an industrial effluent was achieved. Desorption studies concluded that PRO-BEN desorbed the dyes better than alumina. This can thereby be viewed as a recyclable remediation material. The PRO-BEN composite could be a cost efficient alternative towards the removal of organic dyes in wastewater treatment.

Development of a reduced-graphene-oxide based superparamagnetic nanocomposite for the removal of nickel (II) from an aqueous medium via a fluorescence sensor platform

Reduced-graphene-oxide based superparamagnetic nanocomposite (GC) was fabricated and applied for the remediation of Ni(II) from an aqueous medium. The as-prepared GC was extensively characterized by Raman, TEM, AFM, SEM-EDX, SQUID, and BET analyses. Quantitative immobilization of Ni(II) in an aqueous solution by the fluorescent sensor platform of GC was explored at varying pH, doses, contact times, and temperatures. The pseudo-second-order kinetics equation governed the overall sorption process at optimized pH of 5 (±0.2). The superior monolayer sorption capacity was 228mgg(-1) at 300K. Negative ΔG(0) indicated the spontaneous sorption nature, whereas the positive ΔH(0) resulted from an increase in entropy (positive ΔS(0)) at the solid-liquid interface during the endothermic reaction. The lower enthalpy agreed with the relatively high regeneration (approximately 91%) of the GC by 0.1M HCl, because of the formation of stable tetrahedral complex. The physisorption was well corroborated by calculated sorption energy (EDR ∼7kJmol(-1)) and the nature of the Stern-Volmer plot of the fluorescence-quenching data with reaction time. The GC played a pivotal role as a static fluorescent sensor platform (fluorophore) for Ni(II) adsorption. Magnetic property also indicated that GC could be easily separated from fluids by exploiting its superparamagnetic property.

Synthesis, nanostructure evaluation and tunable anomalous 3D hopping transport of manganese ferrite encapsulated poly[3,4-(ethylenedioxy)thiophene] decorated graphene layer

A straightforward novel synthetic approach of manganese ferrite encapsulated poly[3,4-(ethylenedioxy)thiophene] nanocomposite decorated on a graphene layer (NIPG) is engineered assisted by dodecyl benzene sulphonic acid as surfactant. NIPG is characterized by Raman, TG, SEM, EDX, AFM, TEM etc. The temperature-induced (50 to 300 K) I–V characteristics and conductivity are scrutinized for NIPG and the structure–property relationship for electrical transport is also demonstrated. Varying loading of manganese ferrite nanoparticle and graphene significantly improve the order of conductivity even in a low temperature regime due to development of charge carriers such as polaron, bipolaron etc. in the band structure. An anomalous 3D Mott variable range hopping mechanism provides a complete framework to comprehend transport in NIPG.

Synthesis and magnetic properties of highly dispersed tantalum carbide nanoparticles decorated on carbon spheres

The decoration of carbon spheres (CS) by highly dispersed tantalum carbide nanoparticles (TaC NPs) was achieved, for the first time by a unique carbothermal reduction method at 1350 °C for 30 min under reduced oxygen partial pressure. TaC NPs decorated CS composites were then extensively characterized by powder X-ray diffraction and electron microscopy techniques. The composite spheres were approximately 0.8–1 μm in diameter with an average size of 41 nm for the TaC NPs located at the surface. Transmission electron microscopy and Raman analysis showed the formation of the graphene layer at the outer surface of the TaC NPs. An anomalous ferromagnetic response with a spin-glass like behavior has been observed at low temperature in the dc magnetization study with complete suppression of the superconducting response. For ease of synthesis and high reproducibility, this technique opens a new paradigm in the preparation of carbon sphere supported high melting metal carbide nanoparticles for various technological purposes.