Controlled/living polymerization of 2‐(diethylamino)ethyl methacrylate and its block copolymer with tert‐butyl methacrylate by atom transfer radical polymerization

Polymerization of 2‐(diethylamino)ethyl methacrylate (DEAEMA) via homogeneous atom transfer radical polymerization under various reaction conditions is described. The effects of the initiators and solvents were examined. With 1,1,4,7,10,10‐hexamethyl triethylenetetramine/copper(I) chloride/p‐toluenesulfonyl chloride as the ligand/catalyst/initiator system in methanol, poly(DEAEMA) with a polydispersity index as low as 1.07 was synthesized. Kinetic studies demonstrated the polymerization was very well controlled and exhibited the living characteristic of the process. Well‐defined block copolymers of DEAEMA and tert‐butyl methacrylate (tBMA) were successfully synthesized. The copolymers could be synthesized with equally good results by starting with either p(DEAEMA) or p(tBMA) as the macroinitiators. However, only the macroinitiators terminated with chlorine should be used. The corresponding macroinitiators with bromine as a transferable group did not yield well‐defined copolymers. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 2688–2695, 2003     

Impact of micelles on the biocidal efficiency in a diesel–water interface

Biodegradation occurs in the diesel/water interface in petroleum product pipelines. The microbial contamination can result in inhibitor/fuel degradation, leading to unacceptable levels of turbidity, filter plugging, storage tank corrosion and stored product souring. Therefore, selection of the biocide/inhibitor plays an important role in the transportation of petroleum products through pipelines. Three biocides (cationic and nonionic) were employed to study the biodegradation in a diesel‐water interface. The biocidal efficiency against degradation of diesel was examined by employing Fourier‐transform infrared (FTIR) spectroscopy, nuclear magnetic resonance (NMR) spectroscopy and gas chromatography mass spectrometry (GC‐MS) techniques. Bronopol (2‐bromo‐2‐nitro‐propane‐1, 3‐diol) was found to have higher bactericidal efficiency than N‐cetyl‐N,N, N‐trimethyl ammonium bromide (CTAB) and cetyl pyridinum bromide (CPB). But the cationic biocides (CTAB and CPB) showed good biocidal efficiency at the interface. The data are explained in terms of a model that postulates the formation of a ‘micelle’ at the diesel‐water interface. Copyright © 2007 John Wiley & Sons, Ltd.     

Spectral and electrochemical investigation of 1,8-diaminonaphthalene upon encapsulation of p-sulfonatocalix[4]arene

The ligand salt, Me₆[14]diene·2HClO₄ (L·2HClO₄) was prepared by condensation of acetone and ethylene diamine in the presence of perchloric acid. On reduction of this diene ligand salt, L·2HClO₄ with sodium borohydride, the two isomeric ligands, ‘tet-a’ and ‘tet-b’ were produced. The ligands, on reaction with ZnX₂ (X=Cl, ClO₄, NO₃ or CH₃COO) and ZnSO₄ produced the corresponding complexes. These complexes have been characterized on the basis of elemental analyses; IR, UV–Vis and ¹H-NMR spectroscopies; magnetic and conductance data. Based on these data, all of the complexes of the diene ligand L, as well as the perchlorate complexes of all of the ligands attained a square-pyramidal arrangement, whereas the complexes of ‘tet-a’ and ‘tet-b’, with X=NO₃, Cl or CH₃COO and with ZnSO₄ salt, were octahedral. Moreover, all complexes were monometallic except the nitrato complex, [(ZnL)₂(µ-NO₃)](ClO₄)₃ which is bimetallic. The structure of [(ZnL)₂(µ-NO₃)](ClO₄)₃ has been confirmed by X-ray crystallography. In this complex the zinc centres lie within a N₄O donor set, with the four nitrogen donors from L and one of the oxygen atom stemming from the bridging NO₃. The complexes show different electrolytic behavior in different solvents. The antibacterial activities of the ligands and complexes towards different phytopathogenic bacteria have been investigated.     

Experimental study of thermal performance and pressure drop on a solar air heater with different orientations of arc-shape rib roughness

Journal of Thermal Analysis and Calorimetry - An exhaustive experimental investigation was carried out for the thermal performance of artificially roughened solar air heaters (SAHs) under the...     

Synthesis of α-In 2 Te 3 thin films from In/Te bilayer by Si ion irradiation

In this work, In/Te bilayer thin films were prepared using sequential thermal evaporation method and subsequently irradiated using swift heavy ions (SHIs) of 100 MeV silicon (Si) with different fluences (1×10¹³ to 5×10¹³/cm²). The inter-diffusion of In and Te layers was highly controlled by SHI irradiation and the In₂Te₃ formation capability was compared with that of the conventional annealing method. The structural as well as optical properties of a post-sintered SHI-irradiated In/Te bilayer were investigated using X-ray diffraction (XRD) measurements and UV–visible spectroscopy, respectively. We found that irradiated samples showed single-phase In₂Te₃ under post-annealed conditions at 150 °C unlike that prepared using the conventional thermal annealing method, which showed mixed phases under similar conditions. This confirms the effective inter-diffusion in bilayer films by SHI irradiation toward the formation of single-phase In₂Te₃. The estimated optical band gap energy was found to be 1.1±0.5 eV and strongly corroborated the XRD results. In addition, the estimated refractive index (n) value of the SHI-irradiated sample (～3.3) was higher than that of the sample obtained through the conventional annealing method (～2.8). This proves that SHI offers a highly compact nature even at low temperatures. This work has a wide scope for achieving single-phase alloyed films through bilayer mixing by SHI irradiation.     

Energetic,exergetic and enviro-economic analysis of parallel pass jet plate solar air heater with artificial roughness

Journal of Thermal Analysis and Calorimetry - In this work, the thermal performance of single-pass double-duct jet plate solar air heater with various designs of artificial roughness is analyzed by...     

Determination of overall kinetic constants for mediated electrochemical oxidation of phenol from CO<Subscript>2</Subscript> measurements

Mediated electrochemical oxidation is the latest achievement in environmental electrochemistry for the complete oxidation of organic pollutants. Transition or inner transition elements in an acid medium are usually employed as the mediator-electrolyte combination. The organic pollutants upon oxidation are completely converted to carbon dioxide and water. Since the oxidizing ability of the medium is so vigorous, the changes in the reactant concentrations or intermediates formed are usually difficult to analyze, but the product formed (CO₂) can be measured and quantified in most of the cases. Therefore, in MEO reactions the kinetics can be followed either by monitoring the oxidant concentration changes or by measuring the product concentrations. In real applications the oxidant is regenerated continuously in situ and, hence, the oxidant concentration is maintained throughout the system. Therefore, in continuous organic feeding reactions, the product CO₂ could be monitored and kinetics could be followed. We report in this paper a simple procedure for the calculation of the overall kinetic constants for the destruction of phenol from CO₂ measurements. The procedure is based on the summation of the difference between the total amounts of organic added to the system and reacted to obtain CO₂ evolution patterns. The CO₂ patterns were then fitted with the experimental results to obtain the overall kinetic constants. Thermodynamic parameters have been obtained for phenol destruction from the overall kinetic constants.     

Siloxanes with pendent naphthalene diimides: synthesis and fluorescence quenching

Cyclic siloxanes with pendent naphthalene diimide groups were synthesized via hydrosilylation to form amorphous electron-accepting compounds. Photophysical measurements and >99.9% fluorescence quenching of well-known p-type polymers by the siloxanes demonstrate that these siloxanes form a new class of highly efficient n-type materials that provide some control over intermolecular interactions.     

Supramolecular complex of [60]fullerene-grafted polyelectrolyte and surfactant: mechanism and nanostructures

Water-soluble, pH-responsive mono- and di-[60]fullerene end-capped poly(acrylic acid)s (PAA-C60 and C60-PAA-C60) were synthesized using the atom transfer radical polymerization technique. Isothermal titration calorimetry, dynamic light scattering, UV-vis spectroscopy, and transmission electron microscopy were employed to study the supramolecular complexation between fullerene end-capped PAAs and nonionic surfactant, polyethylene glycol (9-10) tert-octylphenyl ether, also known as Triton X100 (TX100) at different pH values. At pH < 4, TX100 bound specifically to C60 domains driven by hydrophobic and pi-pi interactions between TX100 and fullerene molecules. The binding was exothermic, and the magnitude of the interaction decreased gradually with increasing pH. The amount of polymer-bound TX100 was proportional to the fullerene content, which was approximately 1.3 and approximately 2.5 mM for 5 mM (concentration of carboxylic groups) PAA-C60 and C60-PAA-C60, respectively. Morphological transformations resulting in the formation of polymer/surfactant complex (PSC) precipitates in the course of binding were observed for both polymers. The PSC of PAA-C60 possessed a dense spherical structure, whereas the PSC of C60-PAA-C60 possessed a lamellar stacking structure. The PSC precipitates resolubilized in excess amounts of TX100 to form stable aggregates.     

Biocidal effects of photocatalytic semiconductor TiO2

Photocatalytic action of the commercial TiO₂ was the subject of study on the destruction of the microbes within the biofilms. The TiO₂ powder was characterized by X-ray diffraction (XRD) for identifying its type and the particle size was determined. The biofilm was allowed to form over TiO₂ coatings over glass slides irradiated with polychromatic light for different time durations and distances. It indicates that a five-fold decrease in bacterial count due to the formation of H₂O₂ at TiO₂/biofilm interface. The formation of H₂O₂ at the TiO₂/biofilm interface is estimated and it does not destroy the entire bacterial population within the biofilm. Bacterial killing effect is supported by FT-IR analysis.