An innovative conductometric measurement technique using a nonconventional but high-performance (high-precision, high-resolution, rapid response features for online graphic display) in house-built pulsating conductivity monitoring instrument has been deployed to study the kinetic behavior during the reaction of ethyl acetate and NaOH. A laboratorymade constant temperature reaction bath with the facility of continuous stirring of solution for homogeneous mixing was used to carry out experiments at desired solution temperatures. Rate constants of the saponification reaction in the temperature range at various temperatures (30-55 • C) were determined, and the results were compared with the reported values. Although the reported data exhibit wide scatter, our data are in agreement with some of the literature data. From these data, thermodynamic parameters such as activation energy, activation enthalpy, activation entropy, and activation free energy have been evaluated. With the introduction of this novel conductometric measurement technique, the determination of rate constants at various solution temperatures becomes much simpler and faster. C 2011 Wiley Periodicals, Inc. Int J Chem Kinet 43: [648][649][650][651][652][653][654][655][656] 2011
Utilization of recycled polypropylene obtained from post-consumer products and fly ash particles, obtained as a by-product from thermal power plants, has environmental as well as economical benefits for society. A valuable addition can be made to these waste materials by converting them into composite materials. In this study, an attempt has been made to develop a composite material from RPP and fly ash in 1 : 1 weight ratio, using two types of coupling agents. A silane coupling agent (VTMO) and a maleated polypropylene (Epolene G 3003) were used as the coupling agents. The composites were characterized for their flexural properties, water absorption behavior, and thermal degradation behavior. There was a significant improvement in properties when VTMO was used as the coupling agent compared to Epolene.
The reactions of the tridentate hydrazone ligand, N′-[1-(pyridin-2-yl)ethylidene]acetohydrazide (HL), obtained by condensation of 2-acetylpyridine with acetic hyadrazide, with copper nitrate trihydrate in the presence of thiocyanate, or with CuCl2 produce two distinct coordination compounds, namely a one-dimensional helical coordination chain of [CuL(NCS)]n (1) units, and a doubly chlorido-bridged dinuclear complex [Cu2L2Cl2] (2) (where L=CH3C(O)=N–N=CCH3C5H4N). Single-crystal X-ray structural determination studies reveal that in complex 1, a deprotonated hydrazone ligand L− coordinates a copper(II) ion that is bridged to two neighbouring metal centres by SCN− anions, generating a one-dimensional helical coordination chain. In complex 2, two symmetry-related, adjacent copper(II) coordination entities are doubly chlorido-bridged, producing a dicopper entity with a Cu⋅⋅⋅Cu distance of 3.402 (1) Å. The two coordination compounds have been fully characterised by elemental analysis, spectroscopic techniques including IR, UV–vis and electron paramagnetic resonance, and variable-temperature magnetic studies. The biological effects of 1 and 2 on the viability of human colorectal carcinoma cells (COLO-205 and HT-29) were evaluated using an MTT assay, and the results indicate that these complexes induce a decrease in cell-population growth of human colorectal carcinoma cells with apoptosis.
In the title compound, [CuCl2(C9H11N3O)], the CuII atom is in a distorted square-pyramidal CuCl2N2O coordination geometry. The tridentate acetohydrazide ligand chelates in a meridional fashion. The chloride ligand in the axial position forms a long Cu—Cl distance of 2.4892 (9) Å. In contrast, the Cu—Cl distance from the equatorial chloride ligand is much shorter [2.2110 (7) Å]. Intermolecular N—H⋯Cl and C—H⋯Cl hydrogen bonds link the complexes into a three-dimensional network.
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