Publications by authors named "N G Renganathan"

Generation of solid wastes due to industrialization and urbanization results in dumping of wastes in landfills causing contamination of soil, air, and water. One of the important solid wastes is construction and demolition wastes generated during destruction of engineering structures. These wastes reduce the percolation of rain water that recharges the underground water level table and affects the integrity of the environment.

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The diminution of the natural sources in the form of dredging the riverbanks and blasting the mountain ranges has always dented the balance of the ecosystem which in turn results in disasters as well at times. This alarming situation accelerates the global warming, threatens the biota life in riverbanks, diminishes the ground water level, harms the aquatic life, and affects the growth of agriculture. This study is an attempt to synthesis fine aggregates from the industrial byproducts, namely, fly ash and GGBS through the process of geopolymerization.

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To overcome the scarcity of river sand and dumping of construction and demolition wastes, the fine recycled aggregate (FRA) collected from C&D wastes is being utilized as a replacement to river sand. Many earlier studies reported that the higher water absorption of fine recycled aggregate and weak interfacial transition zone (ITZ) resulted in the development of the concrete with less strength and durability requirements. This study surmounts the above two factors through pre-saturation and a two-stage mixing approach (TSMA) technique.

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Melaminium perchlorate monohydrate (MPM), an organic material has been synthesized by slow solvent evaporation method at room temperature. Powder X-ray diffraction analysis confirms that MPM crystal belongs to triclinic system with space group P-1. FTIR and FT Raman spectra are recorded at room temperature.

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Single crystals of melaminium bis (trichloroacetate) dihydrate have been grown successfully by slow evaporation solution growth technique at room temperature. Single crystal X-ray diffraction analysis reveals that the compound crystallizes in monoclinic system with non -centrosymmetric space group C2 with lattice parameters a=17.70 Å, b=8.

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