2021
DOI: 10.1016/j.jlp.2021.104452
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Evaluating time to maximum rate (TMR) and self-accelerating decomposition temperature (SADT) of self-polymerizing vinyl acetate monomer

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Cited by 5 publications
(2 citation statements)
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“…Industrially, VAM should be distilled to remove the inhibitors increasing the conversion of VAM polymerization. In terms of reaction heat, VAM is more stable, with a substantially lower enthalpy change than polyvinyl acetate (∆ H c = 1095.41–1156.64 J g −1 ) [ 26 ]. The earliest onset temperature for 100 mass% VAM was 93.5 °C, and its concentration increased thermal stability for the VAM solution.…”
Section: Resultsmentioning
confidence: 99%
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“…Industrially, VAM should be distilled to remove the inhibitors increasing the conversion of VAM polymerization. In terms of reaction heat, VAM is more stable, with a substantially lower enthalpy change than polyvinyl acetate (∆ H c = 1095.41–1156.64 J g −1 ) [ 26 ]. The earliest onset temperature for 100 mass% VAM was 93.5 °C, and its concentration increased thermal stability for the VAM solution.…”
Section: Resultsmentioning
confidence: 99%
“…Additionally, the 2nd reaction order gave the highest VAM–PVAc polymerization rate [ 28 , 29 ]. Cheng et al [ 26 ] proposed a self-heating model of VAM self-sustaining decomposition with a first-order reaction. The polymerization rate of VAM–PVAc obeyed an nth order reaction as follows: where k is a rate constant as an exponential function of temperature, k 0 is an Arrhenius rate constant, R is an ideal gas constant (8.314 J mol −1 °C −1 ), E a is the activation energy, and [C VAM ] is the concentration of VAM.…”
Section: Resultsmentioning
confidence: 99%