In the reported work, wool fabric was coated with epoxy resin by hand layup method to fabricate wool-epoxy composites. Hydrophobic nanosilica used as a filler improve their mechanical characteristics. The physico-mechanical properties of composites were analyzed using various analytical techniques. surface morphology examined aid Scanning Electron Microscope. biodegradability developed determin...

four amidine nr2b-selective nmda receptor antagonists, n-( 2-methoxy benzyl) -3-phenyl-acrylamidine, n-[diduterio(2-methoxyphenyl) methyl]-3-phenyl-acrylamidine, n-benzyl-3-phenyl-acryl amidine and n-[diduterio(phenyl)methyl]-3-phenyl-acrylamidine, all fourlabeled with carbon-14 in the 1-position, have been synthesized as part of 5-step sequence fromba14co3.

Cement-based materials are ubiquitous in almost all built environment. In spite of this, little is known about the formation and the role played by the silicate chains always present in the cement nanostructure. By means of first principles simulations we provide compelling evidence on the pivotal role played by certain ionic species in the formation of the silicate chains inside the cementitio...

The effect of alkyl substituents on the C-phenyl and/or the N-Phenyl ring of benzophenylhydroxamic acid on their molecular structure and hydrogen bonding has been investigated. The predominant configuration in CHCl3 is determined by steric and electronic effects. Substituents on the C-phenyl ring favor the cis configuration, while substituents in the N-phenyl ring favor a trans c...

two modified methods for assaying sodium diclofenac were developed by gc and hplc. diclofenac was converted into methyl ester derivative by methyl iodide in acetone. the ester was extract and subjected to glc with flame ionization detector. %5 se-30/chrom w-hp (80-100 mesh) was used as a column in gc. for reversed phase hplc, the mobile phase was methanol and water (55-45). the separation was p...

reaction between aromatic aldehydes and 3–methyl-1-phenyl-2-pyrazoline-5-one catalyzed by nano-sio2/hclo4 in water under reflux provided a simple and efficient route for the synthesis of 4-((5-hydroxy-3-methyl-1-phenyl-1h-pyrazol-4-yl)(aryl)methyl)-3-methyl-1-phenyl-1h-pyrazol-5-ol derivatives in high yields.