Instructional-Designed Strategy for Massive Multiplayer Online M-learning

Khalid, Mohd Firdaus; Kameyama, Wataru

doi:10.1109/itme.2008.4743973

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Cited by 3 publications

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“…[5][6][7] Thus it is this weak peroxide linkage (-O-O-) that undergoes cleavage during electron transfer reactions. [8][9][10][11][12][13][14][15] However, such peroxocompounds are exceptionally sensitive to the traces of metal-ions as has been observed in trace metal-ion catalysis in large number of reactions of peroxo acids.…”

Section: 4mentioning

confidence: 99%

The Kinetics and Mechanism for the Oxidation of Nicotinic Acid by Peroxomonosulfate in Acidic Aqueous Medium

Agrawal¹,

Sailani²,

Gupta³

et al. 2012

Journal of the Korean Chemical Society

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ABSTRACT. The kinetics of oxidation of nicotinic acid by peroxomonosulfate (PMS) has been studied in acetate buffers. Stoichiometry of the reaction corresponds to the reaction of one mole of the oxidant with a mole of nicotinic acid. N→O product has been confirmed both by UV visible and IR spectroscopy. The reaction is second order viz. first order with respect to each reactant. Activation parameters have also been evaluated. A plausible reaction mechanism is mentioned and the derived kinetic rate law accounts for experimental observations.

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