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Melamine formaldehyde: curing studies and reaction mechanism
by
Abdala, Ahmed A
, Merline, Dyana J
, Vukusic, Sulafudin
in
639/638/455/303
/ 639/638/455/941
/ 639/638/455/958
/ 639/638/455/959
/ Biomaterials
/ Bioorganic Chemistry
/ Bridges (structures)
/ Chemistry
/ Chemistry and Materials Science
/ Chemistry/Food Science
/ Crosslinking
/ Curing
/ Differential scanning calorimetry
/ Formaldehyde
/ Melamine
/ Methylene
/ original-article
/ Polymer Sciences
/ Resins
/ Surfaces and Interfaces
/ Thin Films
2013
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Melamine formaldehyde: curing studies and reaction mechanism
by
Abdala, Ahmed A
, Merline, Dyana J
, Vukusic, Sulafudin
in
639/638/455/303
/ 639/638/455/941
/ 639/638/455/958
/ 639/638/455/959
/ Biomaterials
/ Bioorganic Chemistry
/ Bridges (structures)
/ Chemistry
/ Chemistry and Materials Science
/ Chemistry/Food Science
/ Crosslinking
/ Curing
/ Differential scanning calorimetry
/ Formaldehyde
/ Melamine
/ Methylene
/ original-article
/ Polymer Sciences
/ Resins
/ Surfaces and Interfaces
/ Thin Films
2013
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Melamine formaldehyde: curing studies and reaction mechanism
by
Abdala, Ahmed A
, Merline, Dyana J
, Vukusic, Sulafudin
in
639/638/455/303
/ 639/638/455/941
/ 639/638/455/958
/ 639/638/455/959
/ Biomaterials
/ Bioorganic Chemistry
/ Bridges (structures)
/ Chemistry
/ Chemistry and Materials Science
/ Chemistry/Food Science
/ Crosslinking
/ Curing
/ Differential scanning calorimetry
/ Formaldehyde
/ Melamine
/ Methylene
/ original-article
/ Polymer Sciences
/ Resins
/ Surfaces and Interfaces
/ Thin Films
2013
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Melamine formaldehyde: curing studies and reaction mechanism
Journal Article
Melamine formaldehyde: curing studies and reaction mechanism
2013
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Overview
Melamine formaldehyde (MF) resin was synthesized by the reaction between melamine and formaldehyde under alkaline condition in tetrohydrofuran medium with 1:3 melamine to formaldehyde molar ratio. The synthesized resins were characterized by differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR) and thermal gravimetric analysis (TGA). Curing and reaction mechanism was studied by thermal and spectroscopic analysis. Two exothermic peaks were observed in the DSC analysis indicating a two-step crosslinking reaction process was correlated to TGA analysis. FTIR studies at different temperatures explained the two-stage curing mechanism which is concurring with the DSC data. At a temperature range of 140–160 °C, reversible demethylolation is dominating to the crosslinking reaction. At temperature >160 °C, the crosslinking reaction dominates. On the basis of DSC and FTIR data, a possible crosslinking reaction route was derived and explained. The first stage of curing is the conversion of methylol groups to primary amine and the second stage is the crosslinking of methylol groups to the final product, methylene bridges. The thermal stability of the methylol groups, methylene bridges and the triazine ring, as well as the evaporation of effluents at different stages of curing, are also discussed based on combined TGA and DSC results.
Curing studies and reaction mechanism of MF resin was studied by thermal and spectroscopic tools comparing DSC and FTIR studies explains the two-stage thermal curing mechanism. The first step of thermal curing at temperature range of 140–160 °C is the reverse reaction of methylol groups to melamine and second step occurring at temperature >160 °C is the crosslinking of methylol groups to the final product, methylene bridge. Hence, by the mutual agreement of DSC and FTIR studies, a possible reaction route was derived for the thermal curing process. The DSC–TGA thermogram supports the two-step process of the cure reaction by exhibiting two peaks in the same temperature region.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
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