Physico-analytical Studies on Salicylaldehyde Thiosemicarbazone Complexes

In this study the complexes of salicylaldehyde thiosemicarbazone with Pd, Cu and Ru were prepared. The prepared complexes were characterized by spectroscopic, element and thermal analyses and D.C. conductivity measurement. The antimicrobial activity of all the prepared compounds against gram-positive, gram-negative and fungi was studied. From these studies, it has been obtained that the ligand is bonded to the metals through O, N and S, but to palladium in [Pd(H2L2)]Cl2 only through N and O. Biological studies confirm that the organic effect on both gram-positive and gram-negative bacteria is very weak and their complexes have no effect on fungi, but Cu-complex has strong influence on both types of bacteria.     

Synthesis and antimicrobial activities of new water‐soluble bis‐quaternary ammonium methacrylate polymers

New methacrylate monomers containing pendant quaternary ammonium moieties based on 1,4‐diazabicyclo‐[2.2.2]‐octane (DABCO) were synthesized. The DABCO group contains either a butyl or a hexyl pendant group comprising the hydrophobic segment of the monomers and one tether group to the methacrylate moiety. The monomers were homopolymerized in water by using 2,2′‐azobis(2‐methylpropionamide) dihydrochloride (V‐50) as an initiator. The monomers and polymers were characterized by elemental analysis, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), FTIR, and ¹³C‐NMR. The antimicrobial activities of the corresponding small molecules (bis‐quaternary ammonium monocarboxylates) and polymers were investigated against Staphylococcus aureus and Escherichia coli. Although the small molecules did not show any antimicrobial activity, the polymers were moderately effective against both Gram‐positive and Gram‐negative bacteria. The minimum inhibitory concentration (MIC) values of the polymers with butyl and hexyl hydrocarbon chains against S. aureus and E. coli were found to be 250 and 62.5 μg/mL, respectively. The minimum bactericidal concentration (MBC) value for the polymer with the butyl group was higher than 1 mg/mL, whereas the MBC value for the polymer with hexyl group was found to be 62.5 μg/mL. Thus, an increase of the alkyl chain length from 4 to 6 significantly increased the antimicrobial activity of the polymer. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 635–642, 2004     

Isolation of a yeast,Trichosporon cutaneum,able to use low molecular weight phenolic compounds: application to olive mill waste water treatment

This study deals with the degradation of phenolic compounds in olive oil mill waste; a highly polluting material in olive oil‐producing countries because of its abundance and the toxicity of its phenolic compound content. This investigation confirms the ability of an isolated yeast, identified as Trichosporon cutaneum, to degrade phenolic compounds extracted from olive mill waste water (OMW). The yeast was adapted to the OMW by an enrichment culture. The results of this biotransformation were a decrease in the phenolic content and hence a reduction in the phytotoxic effects of the effluent after the yeast treatment. The kinetic growth of the isolated yeast on phenol over a range of concentrations (0.3–3.0 g dm^?3) was studied. The ability of the strain to assimilate simple monomeric phenols and alkyl phenols, at a concentration of 1 g dm^?3, in a synthetic liquid medium used as the sole carbon source was investigated in a batch culture. The aromatic ring cleavage pathway occurred in the yeast through catechol oxidation. Using various concentrations of ethyl acetate extract from OMW as the sole carbon source, the yeast exhibited growth on the substrate up to 7 g dm^?3 equivalent of phenols. A significant reduction of COD after the treatment of the OMW extract by the yeast isolate was noticed. The removal of phenol and COD exceeded 80% of the original loading after 8 days of treatment, for extracts containing initial COD in the range 19 to 72 g dm^?3. Copyright © 2004 Society of Chemical Industry     

Raman spectroscopic study of CdS,PVA composite films

A new material, which can be used in solar energy utilization, is obtained here by adding different weights of poly(vinyl alcohol) (PVA) to the semiconducting material CdS. The effect of this addition was studied by using FT‐Raman spectrometer (based on 1500 mW Nd : YAG laser at 1064 nm), UV–Vis‐IR (190–800 nm) spectrophotometer, and X‐ray diffractometer. Our experimental results indicated the appearance of several new Raman bands, which have not existed in both CdS and PVA. Some of the bands which are already existing in the Raman spectra of PVA showed an unexpected systematic increase in their intensities after the addition of CdS to the matrix. On the other hand, some of the new Raman bands appeared in special concentrations of PVA only, whereas some of the Raman bands of CdS were found to disappear after adding PVA. Finally, shifts in some bands associated with random increase in their intensities after adding PVA to CdS was detected in the FT‐Raman analysis. The experimental evidence given here might be attributed to the occurrence of new bonds, indicating that the produced mixture is a new material. The assignment of the new bands as well as an interpretation of the obtained variations is given here. Our X‐ray diffraction data confirmed the interpretation introduced here. Moreover, the UV–Vis spectra confirmed the existence of new absorption bands in the Visible region. The I‐V characteristic curve was measured for a selected concentration of the new composite material, showing a remarkable increase in the values of the conduction current of about two orders of magnitude as compared with the pure PVA material. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1984–1992, 2004     

Synthesis of structured triglycerides from peanut oil with immobilized lipase

Structured triglycerides (ST) that contain medium- and long-chain fatty acids were synthesized by lipase-catalyzed interesterification between tricaprylin and peanut oil. To select appropriate enzymes, we investigated nine commercial lipase preparations for their ability to hydrolyze pure triglycerides as well as natural oils. Three microbial lipases from Rhizomucor miehei (RML), Candida sp. (CSL), and Chromobacterium viscosum (CVL) gave good results, and immobilized preparations were used in the interesterification. RML gave the highest yields of ST (73%, 40°C), although its hydrolytic activity toward triolein was low. As the temperature was raised to 50°C, the yield of ST increased to 79%. After 120 h reaction time, remaining activities were high for CSL (71%), moderate for CVL (48%), and low for RML (20%). Parts of this paper were presented as a poster at the Biochemical Engineering Conference IX, May 1995, Davos, Switzerland.     

Parallel query processing with zigzag trees

In this article, we describe our approach to the compile-time optimization and parallelization of queries for execution in DBS3 or EDS. DBS3 is a shared-memory parallel database system, while the EDS system has a distributed-memory architecture. Because DBS3 implements a parallel dataflow execution model, this approach applies to both architectures. Using randomized search strategies enables the exploration of a search space large enough to include zigzag trees, which are intermediate between left-deep and right-deep trees. Zigzag trees are shown to provide better response time than right-deep trees in case of limited memory. Performance measurements obtained using the DBS3 prototype show the advantages of zigzag trees under various conditions.     

Adsorption and desorption dynamics of associative polymers onto particulates of titanium dioxide,alumina and quartz

The authors have been investigating the adsorption and desorption dynamics of nonionic water soluble polymers on inorganic particles. The influence of the nature of polymers with and without associating hydrophobic end groups, the nature of adsorbents [TiO₂, Al₂O₃ (neutral, acid and basic), and SiO₂], polymer concentrations, linear velocity of fluids, and mutual diffusion of polymer molecules on the patterns of adsorption and desorption distribution of polymer concentrations are shown. The model polymer is a nonionic polyurethane polymer based on ethylene oxide. The polymer's structure is R-O-(DI-PEO)₆-DI-O-R (R is C₁₆H₃₃, DI is isophorone diisocyanate, and PEO is CARBOWAX^TM with a molecular weight of 8200). The phenomenological models of association and dissociation kinetics of associative polymers are suggested. The half-lives of clusters into adsorption and desorption layers are estimated. It is shown that heats of desorption of associative polymers are dependent essentially on heats of dissociation of clusters.     

Measurement of thermophysical properties of polyester cured with styrene in the range 300–450 K

A pulse method for the simultaneous determination of thermal diffusivity, α, specific heat capacity, C_p, and thermal conductivity, λ, are measured for a series of curing of polyester and styrene in the presence of 10, 20, and 30% carbon black in the temperature range 300–450 K. The results show a dependence of the above-mentioned properties on temperature and composition. The mechanism of heat transfer through the specimens is also discussed. © 1993 John Wiley & Sons, Inc.     

Crosslinking of elastomers upon ageing: a kinetic approach based on crystallinity changes followed by DSC

It was observed that crosslinking reactions resulting both from peroxide decomposition or photoageing at wavelengths longer than 300 nm involve a drastic decrease of the crystallinity of some dienic elastomers, such as polybutadienes (rich in cis 1,4 and 1,2 microstructures) and polycyclo‐octene. By comparing precisely the rate of decomposition of dicumyl peroxide and that of the crystallinity decrease, it was possible to show that the kinetics of crystallinity loss observed upon ageing can be identified with that of the crosslinking of elastomers. The results indicate that the crosslinking process can be followed directly by DSC measurement of the crystallization/melting cycle. © 2003 Society of Chemical Industry