“…The FTIR spectra of all the samples show distinct peaks in the identical position with different intensities. Several IR bands at 3642, 3200–3400, 2905, 1642, 1425, 980, and 872 cm –1 appear to be due to the O–H stretching of calcium hydroxide, ν 1 and ν 2 stretching of the water molecule, H–C stretching of methyl or methylene group, ν 2 bending of the water molecule, ν 3 stretching of carbonate, Si–O stretching of polymeric silicate (C–S–H), and ν 2 stretching of carbonate, respectively. , It is reported elsewhere that the relative peak area ratio (peak area of the product phase and the methyl or a methylene group) could be an indicator of the amount of hydrated product. ,, Previously, the relative peak intensity ratio of the IR bands was measured to predict the amount of limestone formation. , In this study, the peak of the organic moieties (methyl or methylene group) appeared at 2905 cm –1 in the IR spectrum of hydrated cement paste may be due to the treating of cement samples with acetone, is considered as a base peak to yield a relative peak area ratio. ,,,, In fact, this is considered as a platform to compare the IR spectroscopic data of control sample and the hydrogen-rich water based cement sample. Sinha and Rout reported a similar analysis of the FTIR spectral data to compare the removal of hemicelluloses from the jute fiber after mercerization.…”