Possibility to Use Hydrothermally Synthesized CuFeS<Subscript>2</Subscript> Nanocomposite as an Acceptor in Hybrid Solar Cell

Here we have approached the plausible use of CuFeS₂ nanocomposite as an acceptor in organic–inorganic hybrid solar cell. To produce CuFeS₂ nanocomposite, hydrothermal strategy was employed. The room-temperature XRD pattern approves the synthesized material as CuFeS₂ with no phase impurity (JCPDS Card no: 37-0471). The elemental composition of the material was analyzed from the TEM-EDX data. The obtained selected area electron diffraction (SAED) planes harmonized with the XRD pattern of the synthesized product. Optical band gap (4.14 eV) of the composite from UV–Vis analysis depicts that the synthesized material is belonging to wide band gap semiconductor family. The HOMO (? 6.97 eV) and LUMO (? 2.93 eV) positions from electrochemical study reveal that there is a possibility of electron transfer from MEH-PPV to CuFeS₂. The optical absorption and photoluminescence spectra of MEH-PPV:CuFeS₂ (donor:acceptor) composite were recorded sequentially by varying weight ratios. The monotonic blue shifting of the absorption peak position indicated the interaction between donor and acceptor materials. The possibility of electron transfer from donor (MEH-PPV) to acceptor (CuFeS₂) was approved with photoluminescence analysis. Subsequently, we have fabricated a hybrid solar cell by incorporating CuFeS₂ nanocomposite with MEH-PPV in open atmosphere and obtained 0.3% power conversion efficiency.     

Poly(ethylene oxide)‐g‐gellan polysaccharide nanocarriers for controlled gastrointestinal delivery of simvastatin

Herein, a novel gellan polysaccharide‐based amphiphilic copolymer was synthesized for the development of simvastatin‐loaded micellar nanoparticles. The nanoparticles were explored for their controlled drug release and improved pharmacodynamic potentials. The copolymer was characterized by Fourier transform infrared spectroscopy (FTIR) and elemental analysis. The onset of copolymer micellization was detected by fluorescence spectroscopy. Simvastatin was loaded into micellar particles by solvent evaporation method and the particles were then characterized by microscopic and light scattering techniques. The physical state of drug was studied by X‐ray diffraction analysis. Pharmacodynamic assessment of the micellar preparations was done on rabbit models. The copolymer formed micellar nanoparticles in water. Critical micellar concentration was 9.12mg/l. The micellar particles (426.8–912.6nm) entrapped a maximum of 18.86% drug. Higher negative zeta potential indicated physical stability of micellar systems. A simple diffusion mechanism was operative in the event of comparatively faster drug release in pH6.8 phosphate buffer solution. No significant drug‐copolymer interaction was traced by FTIR spectroscopy. The amorphization of drug into micellar particles reduced LDL‐cholesterol level by ～45% in hyperlipidemic rabbits and this was about 2.5 times higher than pure drug dispersion. Copolymer micellar nanoparticles of simvastatin could control cholesterol level in hyperlipidemic rabbits and thus had potential in drug delivery applications. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42399.     

Modeling and experimental studies on single particle coal devolatilization and residual char combustion in fluidized bed

Single particle devolatilization followed by combustion of the residual coal char particle has been analyzed in a batch-fluidized bed. The kinetic scheme with distributed activation energy is used for coal devolatilization while multiple chemical reactions with volume reaction mechanism are considered for residual char combustion. Both the models couple kinetics with heat transfer. Finite Volume Method (FVM) is employed to solve fully transient partial differential equations coupled with reaction kinetics. The devolatilization model is used to predict the devolatilization time along with residual mass and particle temperature, while the combined devolatilization and char combustion model is used to predict the overall mass loss and temperature profile of coal. The computed results are compared with the experimental results of the present authors for combustion of Indian sub-bituminous coal (15% ash) in a fluidized bed combustor as well as with published experimental results for coal with low ash high volatile matter. The effects of various operating parameters like bed temperature, oxygen mole fraction in bulk phase on devolatilization time and burn-out time of coal particle in bubbling fluidized bed have been examined through simulation.     

Coalescence of bubbles and stability of foams in aqueous solutions of Tween surfactants

Coalescence of air bubbles and stability of foams in aqueous solutions of Tween 20, 40, 60 and 80 are reported in this work. Adsorption of the surfactants at air–water interface was studied by measuring the surface tension of the surfactant solutions. The surface tension profiles were fitted using a surface equation of state derived from the Gibbs and Langmuir adsorption equations. The critical micelle concentration and surface tension at this concentration were determined. The effect of surfactant concentration on coalescence of air bubbles at flat air–water interface was studied. The role of steric force on coalescence time was investigated. The coalescence time distributions were fitted by the stochastic model. The mean values of the distributions were compared with the predictions of seven film-drainage models. Stability of foams was analyzed by the Ross–Miles test. The initial and residual foam heights were measured at different surfactant concentrations. The stability of foams was compared with the coalescence time of the bubbles.     

Biosorptive removal of cationic dye from aqueous system: a response surface methodological approach

In this study, response surface methodology (RSM) was employed for the removal of methylene blue (MB) from aqueous solution using neem (Azadirachta indica) bark dust (NBD) as a bioadsorbent. The influence of various process parameters namely initial concentration (500–1,000 mg L^?1), bioadsorbent dose [0.20–1.50 g (100 mL)^?1], pH (5–12), and stirring rate (250–650 rpm) was taken as an input parameter. A total of 29 biosorption experimental runs were carried out employing the detailed conditions designed by RSM based on the Box–Behnken design (BBD). Response surface plots were studied to determine the interaction effects of main factors and optimum conditions of process. Regression analysis showed good fit of the experimental data to the second-order polynomial model with coefficient of determination (R ²) value of 0.9760 and model F value of 40.68. The predicted R ² value is 0.8979. In addition, results reported in this research demonstrated the feasibility of employing NBD as bioadsorbent for MB removal.     

Highly dispersed platinum nanoparticles on graphitic carbon nitride: A highly active and durable electrocatalyst for oxidation of methanol,formic acid and formaldehyde

Finding efficient electrocatalyst for oxidation of small organic molecules such as methanol (CH₃OH), formic acid (HCOOH), formaldehyde (HCHO) etc. is essential for the development of their respective direct fuel cells. We report here highly dispersed platinum nanoparticles (PtNPs) on carbon nitride (CN_x) were successfully synthesized by the ultrasound mediated sodium borohydride reduction of H₂PtCl₆ in presence of CN_x nanosheets. This platinum–carbon nitride (Pt/CN_x) composite exhibited superior electrocatalytic activity towards oxidation of CH₃OH, HCOOH and HCHO in acid media. The mass activity, onset potential, tolerance to carbon monoxide (CO) poisoning and long term durability for the catalytic oxidation of CH₃OH, HCOOH, HCHO on Pt/CN_x catalyst in acid media is much higher than that of commercial Pt/C catalyst. The mass activity of Pt/CN_x catalyst at ～0.64 V (forward scan) is 310 mA/mg_Pt which is 2.7 time higher than that of commercial Pt/C for methanol oxidation. The electrooxidation of HCOOH on Pt/CN_x occurs via dual mechanism with greatly enhanced oxidation through dehydrogenation pathway in comparison with commercial Pt/C. The mass activity on Pt/CN_x at 0.3 V (vs. NHE) is 25 times higher than that of Pt/C for oxidation of HCOOH. The superior catalytic activity and durability of this Pt/CN_x catalyst can be attributed to high dispersion of PtNPs and strong catalyst support interaction.     

Economic value and environmental impact (EVEI) analysis of biorefinery systems

The selection of product portfolios, processing routes and the combination of technologies to obtain a sustainable biorefinery design according to economic and environmental criteria represents a challenge to process engineering. The aim of this research is to generate a robust methodology that assists process engineers to conceptually optimise the environmental and economic performances of biorefinery systems. A novel economic value and environmental impact (EVEI) analysis methodology is presented in this paper. The EVEI analysis is a tool that emerges from the combination of the value analysis method for the evaluation of economic potential with environmental footprinting for impact analysis. The methodology has been effectively demonstrated by providing insights into the performance of a bioethanol plant as a case study. The systematisation of the methodology allowed its implementation and integration into a computer-aided process engineering (CAPE) tool in the spreadsheet environment.     

Synthesis and characterization of gelatin based polyester urethane scaffold

For tissue engineering purpose two gelatin based polyester urethane scaffolds of different compositions were prepared from lactic acid, polyethylene glycol 400 (PEG 400) and characterized by FTIR, XRD for their mechanical and morphological properties using SEM and optical microscopic analyses. Degradation and swelling studies of gelatin based polyester urethane scaffolds in phosphate buffer saline (PBS) were performed. Human keratinocyte cells were cultured within these scaffolds, which showed good cell adherence and proliferation.     

A novel endonuclease from kinetoplastid hemoflagellated protozoan parasite Leishmania

A nuclease activity has been purified from the nuclei-kinetoplast fraction of Leishmania. This enzyme, termed endonuclease M (Endo M), is shown by electrophoresis in a denaturing polyacrylamide gel to be associated with a single polypeptide of molecular mass 52 kDa. Physical analysis of the enzyme indicates that it has a sedimentation coefficient S20,w of 4.5S, a Stoke's radius of 32.5 A, and a native molecular mass of 53 kDa. The final Mono Q purified Endo M possesses both DNase and RNase activities. It acts as an endonuclease by introducing random single-stranded nicks into the supercoiled DNA molecules, that often leads to its linearization due to nicking at the opposite strands, and subsequent degradation of the DNA with further incubation. Single-stranded DNA is twice preferred to double-stranded DNA as substrate. Single-stranded RNA is also degraded rapidly and is competitive as a substrate with single-stranded DNA. RNA:DNA hybrids, however, are largely resistant to the Endo M digestion.