Photochemical Reactions in Supramolecular Assemblies of Gels: Dimerizations and Polymerizations via Pericyclic Reactions

Gel state reactions offer new direction for the reactivity of the organic molecules or metal‐organic materials upon photoirradiation with shorter reaction times and high yields compared to solid and solution states. The restricted molecular movement among the molecules in the soft solids control the stereoselectivity of the photoproducts in the gel state reactions. To date, most of the strategies based on self‐assembly have been demonstrated in the solid state, in particular for [2+2] reactions of olefins and polymerization reactions of diacetylenes via 1,4 addition. The soft materials are of emerging materials in recent days given their many applicative day‐to‐day aspects. This review gives a glimpse of recent reports on pericyclic reactions in the gel state that are designed based on the self‐assembly concept. Also it highlights how such reactions accompany the physical changes in the structure of the gels and stereo controlled products with high yields.     

Distribution of technetium in PUREX process streams

Extraction of technetium has been carried out from the aqueous medium containing nitric acid under different experimental conditions to investigate its extraction behaviour in 30% tri-n-butyl phosphate in n-dodecane. In order to study the distribution behaviour of technetium in different streams of PUREX process, experiments were carried out under process conditions. The distribution of technetium was also studied using anion-exchange resin. Based on these results, the path of technetium in the PUREX process streams has been established which will be useful in the development of an advanced PUREX flow-sheet for containment and isolation of technetium in an environmental friendly fuel cycle.     

Emulsifier‐free emulsion polymerization of acrylonitrile: Effect of in situ developed Cu(II)/glycine chelate complex initiated by monopersulfate

The catalytic effect of various Cu(II) salts and Cu(II) chelate complexes of certain amino acids on the emulsion polymerization of acrylonitrile in the absence of added emulsifier was investigated in experiments. The CuSO₄/glycine chelate complex was chosen for a detailed kinetic study of acrylonitrile polymerization. The polymerization was studied at varying concentrations of initiator, monomer, Cu(II), glycine, solvents, and TiO₂ over a temperature range of 30–60°C. The overall activation energy and the viscosity average molecular weight of the polymer were computed. From the kinetic and spectrophotometric studies, the mechanism of KHSO₅ decomposition by the Cu(II)/glycine complex and initiation of polymerization was suggested. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 2785–2790, 1999     

An XPS Study with Depth Profiling for the Surface Oxide Layer Formed on Aluminides Produced on Superalloy 690 Substrates

Superalloy 690 substrates containing mainly Cr and Ni aluminides on the uppermost surface, formed by atmospheric plasma spraying and heat treatment, were oxidized at 1273 K in air for 2 h. Quantitative X-ray photoelectron spectroscopy (XPS) analyses indicated that the outermost surface layer formed on aluminides is composed of ~ 21.0 at.% Al⁺³ (as Al₂O₃), 17.0 at.% Al⁰ (elemental aluminium), 1.4 at.% Cr⁺³ (as Cr₂O₃) and 60.5 at.% O (in Al₂O₃ and Cr₂O₃ and also includes oxygen contaminant). Surface sputtering for 5 min exhibited splitting of Cr2p_3/2 peak into a doublet comprising Cr⁺³ (0.9 at.%) and Cr⁰ (0.4 at.%) with the presence of 1.15 at.% Ni⁰ in the surface layer that mainly contained ~ 37.3 at.% Al⁺³, 7.3 at.% Al⁰ and 52.9 at.% O. Surface sputtering for 15 min indicated surface composition similar to surface sputtered for 5 min but with a marked reduction in ratio of Al⁺³/Al⁰ (32.2 at.% Al⁺³/11.90 at.% Al⁰) in the surface layer.     

Investigation of Pt and Pd Modified WO<Subscript>3</Subscript> and ZnO Based Thin Film Sensors for Ethanol Sensing

Ethanol sensors based on different WO₃ and ZnO structures are studied in the present work. The XRD and SEM processes are used to characterize the sensing layer’s surface morphology which reveals the presence of nanoparticle in sensing layer. Further reducing the nanoparticle diameter by the addition of palladium (Pd) and platinum (Pt) for both the sensors (ZnO and WO₃) gives good results on sensitivity, operating temperature, response time and recovery time. Nanoparticle diameter for undoped WO₃, Pd-modified WO₃ and Pt-modified WO₃ based sensors is 11.8, 6 and 5.4 nm, whereas nanoparticle diameter for undoped, Pd-modified and Pt-modified ZnO based sensors is 20, 14 and 11 nm, respectively. Analysis of dynamic response of the sensors when exposed to different concentrations of ethanol vapour (from 500 to 10,000 ppm) and various temperatures indicate the improvement in sensitivity up to 77.2% for WO₃ and 74.6% for ZnO based sensors.     

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.     

Structural correlation to magnetodielectricity and coercivity at room temperature in multiferroic Bi0.7Ba0.3−xPbxFeO3

We report an interesting structural correlation to the static dielectric constant (?₀), magnetodielectric (MD) response and coercivity at room temperature for Bi_0.7Ba_0.3?xPb_xFeO₃ at x = 0, 0.05, 0.10 and 0.15, above which a structurally single-phase material could not be achieved. The Pb doping leads to a ～2.4 times increase in ?₀. The Fe–O–Fe bond angle increases and approaches 180° with the Pb doping, which is associated with a considerable decrease in coercivity. Interestingly, the MD response is correlated with the average Bi–Fe bond length. This structural correlation is crucial for understanding the origin of moderately high MD response and improving the effects of this for technological applications.     

Influence of Nano Silica on Mechanical and Durability Characteristic of Mortar made by Partial Replacement of Natural Fine Aggregate with Recycled Fine Aggregate

Silicon - To implement sustainability concepts in the construction industry, the possibility of utilizing the recycled fine aggregate obtained from the crushing of coarse aggregate debris of...     

Establishment of a stable Amaranthus tricolor callus line for production of food colorant

This study aimed at demonstrating the effects of fermentation time (24, 48, 72, 96, and 120 h) and water activity (0.943, 0.970, and 0.985) on the production of cellulolytic enzymes by solid-state fermentation of purple mombin (Spondias purpurea L.) residue using Aspergillus niger. The fermentation was carried out at 35°C and the enzyme production was measured as endoglucanase and total cellulose activities. The optimum condition for endoglucanase was water activity 0.974 and 93.8 h of fermentation, reaching a production of 3.21 U/g of residue; whereas for total cellulase it was 0.958 and 79.4 h achieving 12.1 U/g of residue. Fermentation time had a greater effect on the endoglucanase activity, while water activity had a more significant influence on the total cellulase activity. Endoglucanase had optimum activity at temperature of 50°C and pH 5.0. Although cellulase total optimum activity was also at pH 5.0, the maximum activity was at 60°C.