The electrochemical, dielectric, and ferroelectric properties of Gd and Fe doped LaNiO3 with an efficient solar-light driven catalytic activity to oxidize malachite green dye.

This work investigates the effects of double ion substitution on the ferroelectric, electrochemical, dielectric and photocatalytic properties of Gd and Fe doped La1-yGdyNi1-xFexO3 nanoparticles (NPs). La1-yGdyNi1-xFexO3 was fabricated by facile micro-emulsion path and its properties were studied by thermogravimetric analysis (TGA), X-ray diffraction (XRD), scanning electron microscopy (SEM), Raman scattering, Fourier Transform of Infrared (FTIR), energy dispersive x-rays (EDX) techniques. It has a distorted rhombohedral shape with crystallite size within the range of 17-23 nm. The doped material has a spherical heterogeneous morphology, and its surface area increased with increased doping. The electrochemical (CV, EIS, and I-V), conductivity and dielectric (dielectric constant and low dielectric & tangent loss) properties of La1-yGdyNi1-xFexO3 were dependent on the contents of the dopants (Gd and Fe). The doped material had improved specific capacitance compared to the undoped LaNiO3 due to the synergistic effect of Gd and Fe on the doped materials. The conductivity of Gd and Fe doped LaNiO3 5.16 × 104 Sm-1 was enhanced compared to the undoped LaNiO3 3.52 × 10-2 Sm1. Furthermore, hysteresis loop was used to investigate the coercivity (Hc), saturation magnetization (Ms) and remanence (Mr) of the material. The Ms and Mr values were enhanced with the content of the dopants. The photocatalytic activity (PCA) of the material in degrading malachite green (MG) dye was studied. La1-yGdyNi1-xFexO3 NPs was able to degrade up to 96.4% of the dye under visible light irradiation in 50 min. La1-yGdyNi1-xFexO3 has remarkable dielectric, electrochemical, ferroelectric and photo-catalytic properties and have potential applications in microwave, electrical, electronic, energy storage devices. It is also an active photo-catalyst material for the removal/oxidation of toxic pollutants from the environment.

Kinetics and controlled release of lidocaine from novel carrageenan and alginate-based blend hydrogels.

The controlled release of drug from drug carrier has been a point of concern for the researchers to ensure the bioavailability of drug with reduced side effects. The formulation in this study is based upon biopolymers; carrageenan (CG), sodium alginate (SA) and various molecular weights of polyethylene glycol (PEG), cross-linked with (3-Aminopropyl)triethoxysilane, APTES for the sustained release of model drug (lidocaine). The physicochemical properties of the formulated hydrogel blends include bonding pattern (using Fourier Transform Infra-Red Spectroscopy (FTIR), Thermogravimetric analysis (TGA), X-ray diffraction (XRD), swelling study, antimicrobial activity and morphology of hydrogel films was analyzed by scanning electron microscopy (SEM). The as-prepared hydrogels show an improved cell compatibility against 3T3 cell line as well as cell proliferation and kinetics of drug release showed that these hydrogels are potential for controlled release of lidocaine, a numbing agent. GAP 60 exhibited maximum swelling percent (910%) and was employed to load the drug. By using in vitro model, the drug release was studied in PBS solution. Non-Fickian and other kinetic models (Zero order, Higuchi, Hixson, Korsmeyer Peppas and Baker-Lonsdale) for diffusion were followed in results. The improved properties showed that the formulated hydrogels can easily be used for the sustain drug release studies.

Loading of Cefixime to pH sensitive chitosan based hydrogel and investigation of controlled release kinetics.

Chitosan (biopolymer) and polyvinyl pyrolidone (PVP) with aminopropyletriethoxy silane (cross linker) based hydrogels were prepared and tested for controlled drug release. The drug release and kinetics were studied as a function of pH. Formulations were characterized by Fourier Transform Infrared (FTIR) and Thermogravimetric (TGA) analysis and TAP 32 hydrogel formulation was the most stable and hydrogel samples showed promising antibacterial activity against E. coli strain. The maximum swelling (4386%) was observed for TAP 32 formulation in distilled water, which was decreased with the concentration of ions. The diffusion exponent (n) values of all hydrogel formulations were recorded to be <0.5, which is an indication of Quasi-Fickian diffusion. The maximum swelling was observed at pH 2 and decreased at higher pH. The pH sensitivity of hydrogels found to be promising for their use in drug delivery, which was tested for cefixime drug. Drug release of 81.6% was observed for the period of 12 h in a simulated gastric fluid (SGF). The values of R2 for zero order, first order, Higuchi, Hixson, Korsmeyer-Peppas and Baker-Lonsdale were 0.97, 0.9818, 0.99, 0.99, 0.88 and 0.80, respectively. The hydrogels based on chitosan and PVP revealed potential for controlled cefixime drug release in gastric pH medium.

Fabrication of novel carrageenan based stimuli responsive injectable hydrogels for controlled release of cephradine.

Kappa carrageenan was used to prepare hydrogels having novel compositions with poly(vinyl alcohol) (PVA) and a crosslinker (3-aminopropyl)triethoxysilane (APTES). FTIR was used to confirm the structure and composition of hydrogels. The swelling behavior of hydrogels was studied under different conditions of pH and electrolytic aqueous media. The most efficient swelling result (200%) was observed by the sample containing a low fraction of crosslinker. It also showed different swelling responses in different pH solutions that made it suitable for drug delivery. Thermogravimetric analysis (TGA) illustrated that with the increase in crosslinker amount, the stability of hydrogel was increased. The biodegradation analysis of the hydrogels exhibited the break down by various enzymes into small chain polysaccharides that further broke down in the metabolic pathways. It was revealed that all the hydrogel samples showed strong antibacterial activity against S. aureus and a little against E. coli. Cephradine was used as a model drug and its in vitro release was studied in simulated intestinal fluids (SIF). This release account of the cephradine demonstrated that the release of the drug increased as the time and pH increased, reaching its maximum amount of 85.5% after 7.5 h.

Stimuli responsive biopolymer (chitosan) based blend hydrogels for wound healing application.

Stimuli responsive chitosan (CS) and poly (N-vinyl-2-pyrrolidone) (PVP) have attained hydrogel properties in the presence of 74% neutralized poly acrylic acid (PAA) which can be exploited for wound healing applications. The FTIR spectra confirmed the presence of all specific functional groups and the developed interactions in the hydrogels. The thermal analysis explained that the hydrogel samples are thermally more stable than individual chitosan and PVP. The antimicrobial analysis revealed that all the samples show antibacterial activity against E. coli and the biodegradation analysis is performed to confirm the hydrogels degradation. The hydrogels showed enhanced responsive swelling behavior against different media depending upon the amount of PVP. The %age swelling in water is decreased with the increase in the amount of PVP. The most considerable swelling behavior is observed against pH, as they manifested low swelling at acidic pH and high swelling at neutral pH while at pH 8, the prominent values are obtained. This distinctive behavior of hydrogels and their biocompatibility made them pertinent to drug delivery and their release profile is examined spectrophotometrically using silver sulfadiazine (antibiotic for burnt wounds) showed 91.2% of drug release for a period of 1 h in phosphate buffer saline (PBS) in a consistent and controlled manner.

Cu nanoparticles synthesis using biological molecule of P. granatum seeds extract as reducing and capping agent: Growth mechanism and photo-catalytic activity.

In view of extended applications of nanoparticles, the nanoparticles synthesis is an extensive research field and green synthesis is one of the co-friendly methodologies. Plant extract mediated synthesis of nanoparticles has gained much attention in current decade. In current investigation, copper nanoparticles (CuNPs) were prepared using P. granatum seeds extract (biological molecules) from copper(II) chloride salt. The synthesized CuNPs were characterized by UV-vis spectroscopy, X-ray diffraction measurements (XRD), scanning electron microscopy (SEM), Energy Dispersive X- Ray Spectroscopy (EDX), Fourier transform infra-red spectroscopy (FTIR) and atomic force microscopy techniques. The CuNPs formation occurred through reduction of metal ions followed by nucleation. The size of the CuNPs was in the range of 40-80nm (average particle size was 43.9nm) with semi spherical shape and uniformly distribution. Photocatalytic activity was evaluated by degrading methylene blue dye (150mg/L) at various CuNPs doses (10mg/L-100mg/L). The synthesized CuNPs showed excellent PCA for the degradation of methylene blue (MB) under solar light irradiation and up to 87.11% degradation was achieved. The oxidative degradation mechanism for MB was proposed. In view of efficient PCA, the use of biological molecules of P. granatum seeds extracts for the synthesis of CuNPs.

Nickel nanoparticle synthesis using Camellia Sinensis as reducing and capping agent: Growth mechanism and photo-catalytic activity evaluation.

Recently, the biosynthesis of nanoparticle attracted the attention of scientific community due to its simplicity, ease and eco-friendly nature. In the present study, Camellia Sinensis (C. Sinensis) leaves extract was employed for the synthesis of nickel nanoparticles (NiNPs). The fabricated NiNPs were characterized by scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX) and X-ray diffraction techniques. The photocatalytic activity (PCA) was evaluated by degrading crystal violet (CV) dye. The NiNPs size was in the range of 43.87-48.76nm, spherical in shape and uniformly distributed with magnetization saturation of 0.073 emu/g. The NiNPs showed promising PCA under solar light irradiation. At optimized conditions, up to 99.5% CV dye degradation was achieved. Results revealed that biosynthesis can be adopted for the synthesis of NiNPs in nano-size range since it is simple, cost effective and eco-friendly in nature versus physico-chemical methods.

Photosensitization of TiO2 nanofibers by Ag2S with the synergistic effect of excess surface Ti3+ states for enhanced photocatalytic activity under simulated sunlight.

TiO2 nanofibers, with mean diameter ~200 nm, were fabricated by electrospinning and successfully photosensitized with low bandgap Ag2S nanoparticles of 11, 17, 23 and 40 nm mean sizes, with corresponding loading of 4, 10, 18 and 29 wt.% Ag2S, respectively. 17 nm Ag2S@TiO2 nanofibers exhibited optimal activity in the photodegradation of methylene blue under simulated sunlight with pseudo-first order rate constant of 0.019 min-1 compared to 0.009 min-1 for pure TiO2 nanofibers. In spite of greater visible-light absorption and reduced bandgap, larger than 17 nm Ag2S nanoparticles exhibited sluggish photodegradation kinetics probably due to less photo-induced carriers generation in TiO2 and reduced electron injection rates from the larger sized Ag2S into TiO2. Furthermore, a UV-O3 surface treatment induced excess Ti3+ surface states and oxygen vacancies which synergistically enhanced the photodegradation rate constant to 0.030 min-1 for 17 nm Ag2S@TiO2 sample which is ~70% better than the previously reported for Ag2S/TiO2 hierarchical spheres. This was attributed to the efficient charge separation and transfer driven by increased visible-light absorption, bandgap narrowing and reduced electron-hole recombination rates. The present study demonstrate the potential utilization of Ag2S@TiO2 nanofibers in filtration membranes for removal of organic pollutants from wastewater.

Equilibrium, thermodynamics, and kinetic sorption studies for the removal of coomassie brilliant blue on wheat bran as a low-cost adsorbent.

The sorption studies of coomassie brilliant blue (CBB) from aqueous solution have been carried out on wheat bran (WB). Coomassie brilliant blue on wheat bran was used to study the adsorption behavior under various parameters such as pH, dosage amount, and contact time. It was observed that under optimized conditions up to 95.70% dye could be removed from solution onto WB. Langmuir and Freundlich adsorption isotherms were used to elaborate the results. Freundlich model was found to be fitted well and favored multilayer adsorption. The Freundlich constants n and KF were determined as 0.53 and 2.5 × 10(-4). Thermodynamic parameters such as ΔG, ΔH, and ΔS studied were taking into account, showed spontaneous and favorable reaction for coomassie brilliant blue on wheat bran. The maximum adsorption capacity q(m) was found to be 6.410 mg/g. The investigations show that non treated WB is a low-cost adsorbent for the removal of dyes from textile industry effluents.