Photocatalytic disinfection of water with Ag–TiO2 nanocrystalline composite

A method of solution impregnation and calcination has been demonstrated for synthesizing nanoparticles of Ag–TiO₂ composite photocatalysts for use in the disinfection of water. Only a small proportion of the TiO₂ surface is covered by nano-islands of Ag corresponding to a loading of 4 wt.% of Ag; thus, most of the TiO₂ surface is available for photocatalytic function. Although the primary particles of both Ag and TiO₂ are in the 10- to 20-nm range, microscopic studies indicate that the primary particles of Ag are deposited on nano-agglomerates of 30- to 70-nm-sized TiO₂. It is seen that the relatively small loading of Ag has not caused any UV–vis spectral shift but has enhanced the rate of photocatalytic antibacterial action of TiO₂, presumably by electron trapping.     

Synthesis of Novel Symmetric Porphyrin Schiff Base Dimers by Solid–Liquid Reaction Methodology

A new convenient solid–liquid condensation reaction procedure for the synthesis of novel asymmetric and symmetric meso‐tetraarylporphyrin and metalloporphyrin Schiff bases is reported. The condensation reaction between β‐formyl porphyrin or metalloporphyrins and aromatic amines was carried out at solid–liquid interface by using neutral alumina powder as a solid support for β‐formyl porphyrin or metalloporphyrins and absolute ethanol as the carrier solvent for aromatic amines. Six different asymmetric porphyrin/metalloporphyrin Schiff bases were synthesized via solid–liquid interface reaction methodology. The same solid–liquid synthetic methodology was applied for the synthesis of six novel symmetric Schiff base porphyrin/metalloporphyrin dimers. The comparison of UV–visible spectra of porphyrin Schiff base monomers and dimers revealed that some degree of electronic perturbation has occurred upon dimerization as the Soret bands of the monomers underwent peak broadening along with red shifts. Column chromatography and crystallization were used to purify the compounds. Fourier transform infrared, UV–visible, elemental analysis, ¹H NMR, and mass spectrometry were used to characterize the newly synthesized compounds.     

Multi-solitons of Thermophoretic Motion Equation Depicting the Wrinkle Propagation in Substrate-Supported Graphene Sheets

The paper addresses the thermophoretic motion (TM) equation, which is serviced to describe soliton-like thermophoresis of wrinkles in graphene sheet based on Korteweg-de Vries (KdV) equation. The generalized unified method is capitalized to construct wrinkle-like multiple soliton solutions. Graphical analysis of one, two, and three-soliton solutions is carried out to depict certain properties like width, amplitude, shape, and open direction are adjustable through various parameters.     

Development of new-generation low-carbon steel: Part II-wear behaviour

A new-generation unalloyed low-carbon steel (containing 0.1?wt.% C) has been recently developed by the research group of the present corresponding author through incomplete austenitisation-based cyclic ice-brine quenching possessing an exceptionally high strength (UTS?=?1.7?GPa) along with elimination of a yield point phenomenon. This is attributed to the evolution of a novel microstructure that consists of fine plate martensite crystals with a dispersion of nano-sized cementite particles and clusters. The present research work is conceived as the Part II of this investigation to establish this new-generation ultrahigh strength low-carbon steel as a unique wear-resistant steel substituting the conventional dual-phase steel along with the readily awaited in-depth correlation between wear mechanism and structural evolution. The wear behaviour of heat-treated steels is investigated against an alumina disc using a pin-on-disc tribometer. The steel subjected to incomplete austenitisation-based cyclic ice-brine quenching exhibits much better wear resistance than conventional dual-phase steel. Dominant microcutting and microploughing abrasion aggravate wear loss, especially at higher load, in dual-phase steel that inherently possesses lower matrix hardness. But, very high-surface hardness is attained in the incomplete austenitisation-based cyclic ice-brine quenched steel by virtue of a significant strain hardening of martensite matrix in between hard nano-sized cementite particles. Besides, the wear rate is not allowed to shoot up even at the highest load through the generation of hard abrasion-resistant tribo-oxide layer of Al₂FeO₄. This envisages an advent of novel wear-resistant steel as a better substitution for the dual-phase steel.     

Effect of ZnO on Photocatalytic Degradation of Rh B and Its Inhibition Activity for C. coli Bacteria

Russian Journal of Applied Chemistry - Zinc oxide (ZnO) nanoparticles have been synthesized by co-precipitation method. The structural properties like average crystallite size, lattice parameters,...     

Thermodynamic and kinetic stability of synthetic multifunctional rigid-rod beta-barrel pores: evidence for supramolecular catalysis

The lessons learned from p-octiphenyl beta-barrel pores are applied to the rational design of synthetic multifunctional pore 1 that is unstable but inert, two characteristics proposed to be ideal for practical applications. Nonlinear dependence on monomer concentration provided direct evidence that pore 1 is tetrameric (n = 4.0), unstable, and "invisible," i.e., incompatible with structural studies by conventional methods. The long lifetime of high-conductance single pores in planar bilayers demonstrated that rigid-rod beta-barrel 1 is inert and large (d approximately 12 A). Multifunctionality of rigid-rod beta-barrel 1 was confirmed by adaptable blockage of pore host 1 with representative guests in planar (8-hydroxy-1,3,6-pyrenetrisulfonate, KD = 190 microM, n = 4.9) and spherical bilayers (poly-L-glutamate, KD < or = 105 nM, n = 1.0; adenosine triphosphate, KD = 240 microM, n = 2.0) and saturation kinetics for the esterolysis of a representative substrate (8-acetoxy-1,3,6-pyrenetrisulfonate, KM = 0.6 microM). The thermodynamic instability of rigid-rod beta-barrel 1 provided unprecedented access to experimental evidence for supramolecular catalysis (n = 3.7). Comparison of the obtained kcat = 0.03 min(-1) with the kcat approximately 0.18 min(-1) for stable analogues gave a global KD approximately 39 microM3 for supramolecular catalyst 1 with a monomer/barrel ratio approximately 20 under experimental conditions. The demonstrated "invisibility" of supramolecular multifunctionality identified molecular modeling as an attractive method to secure otherwise elusive insights into structure. The first molecular mechanics modeling (MacroModel, MMFF94) of multifunctional rigid-rod beta-barrel pore hosts 1 with internal 1,3,6-pyrenetrisulfonate guests is reported.     

Synthesis, characterisation and mass spectrometric fragmentation of O-(chlorodifluoroacylated) alcohols

An indirect and uncatalysed esterification of chlorodifluoroacetic acid with polyfluoro and hydrocarbon alcohols has been developed. The method which involves the reaction between sodium chlorodifluoroacetate and alcohols in dimethylformamide (DMF) is particularly facile with polyfluorinated alcohols resulting in esters in 71-85% yield. The esters have been characterised on the basis of ¹H and ¹⁹F NMR and mass spectral data. The electron impact (EI) mass spectrometric fragmentation of these polyfluorinated esters have shown some interesting features which have been substantiated by using tandem mass spectrometry.     

Chiral bis(amino alcohol)oxalamide gelators-gelation properties and supramolecular organization: racemate versus pure enantiomer gelation

Four new chiral bis(amino alcohol)oxalamides (1-4: amino alcohol=leucinol, valinol, phenylglycinol, and phenylalaninol, respectively) have been prepared as low-molecular-weight organic gelators. Their gelation properties towards various organic solvents and mixtures were determined and these were then compared to related bis(amino acid) oxalamide gelators. Spectroscopic (FTIR, (1)H NMR) and X-ray diffraction studies revealed that the primary organization motif of (S,S)-1 and racemate 1 (rac-1) in lipophilic solvents involved the formation of inverse bilayers. The X-ray crystal structure of (S,S)-1 also shows this type of bilayer organization. The crystal structure of rac-2 reveals meso bilayers of hydrogen-bonded aggregates. Within the bilayers formed, the gelator molecules are connected by cooperative hydrogen bonding between oxalamide units and OH groups, while the interbilayer interactions are realized through lipophilic interactions between the iBu groups of leucinol. Oxalamide meso-1 lacks any gelation ability and crystallizes in monolayers. In dichloromethane rac-1 forms an unstable gel; this is prone to crystallization as a result of the formation of symmetrical meso bilayers. In contrast, in aromatic solvents rac-1 forms stable gels; this indicates that enantiomeric bilayers are formed. Oxalamide rac-1 is capable of gelling a volume of toluene three times larger than (S,S)-1. A tranmission electron microscopy investigation of rac-1 and (S,S)-1 toluene gels reveals the presence of thinner fibers in the former gel, and, hence, a more compact network that is capable of immobilizing a larger volume of the solvent. The self-assembly of these types of gelator molecules into bilayers and subsequent formation of fibrous aggregates can be explained by considering the strength and direction of aggregate forces (supramolecular vectors) in three-dimensional space.     

Spectrophotometric Determination of Lisinopril in Pure and Pharmaceutical Formulations

An accurate, simple, fast, and cheap spectrophotometric method has been developed for the determination of lisinopril in pharmaceutical pure and dosage forms. The method is based on the reaction of ninhydrin with primary amine present in the lisinopril in the presence of DMF. This reaction produces a greenish blue colored product which absorbs maximally at 600 nm. Beer's law was obeyed in the range of 10–150 μg/mL with molar absorptivity of 4.083 × 10³ L mole^?1 cm^?1. The effects of variables such as temperature, heating time, concentration of color producing reagent, and stability of color were investigated to optimize the procedure. The results are validated statistically. The proposed method was applied to commercially available tablets, and the results were statistically compared with the official potentiometric method.