Optimized spacer layer thickness for plasmonic-induced enhancement of photocurrent in a-Si:H

Journal of Nanoparticle Research - Plasmonic interfaces consisting of silver nanoparticles of different sizes (50–100&;nbsp;nm) have been processed by the self-assembled dewetting...     

Catalytic carbonylation for the synthesis of chemical intermediates

Chemistry related to three catalytic carbonylation reactions is discussed. Synthesis of diphenylurea from nitrobenzene, aniline, and CO gives isolated yields above 98% at 100–120 °C and 15–60 bar of CO in the presence of a palladium (II) complex, PPh₃ and NEt₄Cl. Experimental evidence was provided to prove a new reaction stoichiometry and involvement of a carbamoyl intermediate. In carbonylation of HCHO over ion exchange resin catalysts, reaction temperature, time, pressure, and solvent were important variables to obtain high yields of methyl glycolate. Carbonylation of isobutylphenylethanol at 120°C and 40 bar of CO in the presence of PdCl₂−PPh₃−HCl gives 98% yield of α-(4-isobutylphenyl) propionic acid (ibuprofen). Each catalyst component had a definite role that is indispensable for an efficient overall reaction.     

Sodium p‐nitro­benzoxasulfamate monohydrate

The title compound, alternatively named sodium 6‐nitro‐3H‐1,2,3‐benzoxa­thia­zole 2,2‐dioxide monohydrate, Na⁺·C₆H₃­N₂O₅S^?·H₂O, consists of chains of NaO₇ units, with the seven donor‐O atoms coming from two water mol­ecules and five p‐­nitro­benzoxasulfamate anions. The seven‐coordinate geometry around the Na⁺ ion is described as monocapped trigonal prismatic, but with a large distortion from ideal geometry. Each triangular face is defined by one O atom each from a water mol­ecule, a nitro group and a sulfonyl group. An O atom from a sulfonyl group caps one of the square faces of the trigonal prism in an unsymmetrical fashion. The water mol­ecules and one sulfonyl O atom are involved in bridging adjacent units, as is the nitro group of the anion. The sulfamate ions adopt an antiparallel alignment between the NaO₇ units and are connected to each other by C—H?O and π–π interactions. The three‐dimensional crystal structure is stabilized by a network of strong O—H?N hydrogen bonds.     

New 3-hydroxyflavone derivatives for probing hydrophobic sites in microheterogeneous systems

Nine new 3-hydroxyflavone derivatives as fluorescent molecular sensors having two well-separated emission bands were synthesized. These sensors can occupy well-determined locations and orientations in macromolecular ensembles, such as micelles due to their finely-tuned designs. These polarity-sensitive dyes can incorporate into the anhydrous hydrophobic core of aqueous micelles.     

Plasma Induced Graft Polymerization of Three Hydrophilic Monomers on Nylon 6,6 Fabrics for Enhancing Antistatic Property

In this study, three hydrophilic monomers; 2-acrylamido-2-methyl-1-propanesulfonic acid, 2-hydroxyethyl methacrylate, diallyldimethylammonium chloride (DADMAC) were selected and their performance as an antistatic finish on nylon 6,6 fabrics was investigated. A non-thermal, high density atmospheric pressure plasma was used to graft polymerize the monomers on nylon 6,6 fabrics. Fabrics were first treated with solutions of monomer in water, air dried and then treated with helium plasma to graft polymerize the monomer on the fiber surface. Surface resistivity values were measured before and after soxhlet extraction with water. Results showed that the DADMAC monomer provided better antistatic properties to fabrics. Further studies with DADMAC monomer were made; effects of plasma post exposure time, plasma pre-exposure time, plasma power, concentration of the monomer and existence of a crosslinker were investigated. Higher plasma power, higher concentration of the monomer and longer post exposure times all gave better antistatic properties to the nylon 6,6 fabrics. Acid dye staining, UV–Vis and FT-IR measurements were conducted and results confirmed a grafted poly-DADMAC layer on the fabric surface.     

The Effect of Selenium Supplementation on the NMR Proton Relaxation Time T1 in Plasma

Selenium has been identified as an essential dietary trace e1ementQ)which is a component of glutathione peroxidase (GSH-Px)(₂)and a cytochrome C-like protein(₃), The enzyme,the four subunits of which each contain one atom of selenium in the form of selenocysteine, the selenium containing active centre being amenable to chemical modification, catalyses the reduction of H,O,and organic hydroperoxides to water.In this way GSH-Px plays an important role in the protection of the cell from oxidative stresses such as the superoxide anion,organic hydroperoxides and H₂O₂     

Combustion characteristics and kinetic analysis of Turkish crude oils and their SARA fractions by DSC

In this study, two Turkish crude oils from southeastern part of Turkey and their saturate, aromatic, resin fractions were analyzed by differential scanning calorimetry (DSC). The experiments were performed at three different heating rates (5, 10, 15 °C min^?1) under air atmosphere. Two different reaction regions were observed from DSC curves due to the oxidative degradation of crude oil components. In the first reaction region, it was deduced that the free moisture, volatile hydrocarbons were evaporated from the crude oils, light hydrocarbons were burned, and fuel was formed. The second reaction region was the main combustion region where the fuel was burned. From DSC curves, it was observed that as the sample got heavier, the heat of the reaction increased. Saturates gave minimum heat of reaction. As the heating rate increased, shift of peak temperatures to high values and extended reaction region intervals were observed. The kinetic analysis of the crude oils and their fractions were also performed using ASTM E-698 and Borchardt and Daniels methods, respectively. Activation energy values of the crude oil samples and the fractions’ high-temperature oxidation region were close to each other and varied between 67 and 133 kJ mol^?1 in ASTM and 35 and 154 kJ mol^?1 in Borchardt and Daniels methods, respectively.     

Chemical modification of silica gel with synthesized Schiff base hydrazone derivative and application for preconcentration and separation of U(VI) ions from aqueous solutions

Schiff base hydrazone derivative (HL) sorbent was synthesized according to the literature to be used in the adsorption and preconcentration of U(VI) ions from aqueous solution and it was exposed to immobilization, and new solid support material was obtained. For this purpose, Schiff base hydrazone derivative (HL) was chemically bonded to silica gel surface immobilized 3-aminopropyl trimethoxysilane, then analyzed by Fourier transform infrared, Brunauer–Emmett–Teller, scanning electron microscopy and elemental analysis. The influence of the solution pH, amount of sorbent, contact time, temperature, foreign ion effect and initial U(VI) concentration was investigated. The maximum U(VI) uptake capacity was found to be 8.46 mg/g.