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1995
DOI: 10.1016/0040-6031(95)02262-z
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Thermogravimetry/Fourier transform infrared coupling investigations to study the thermal stability of melamine formaldehyde resin

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Cited by 129 publications
(78 citation statements)
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“…This can be related to different chemistries of both precursors and formation of large polymers as a result of melamine decomposition by heat treatment. [46] While preoxidation increased the relative amounts of pyrrole/pyridone and pyridinic nitrogen in the melamine derived samples, in ureatreated samples a significant increase was noticed for pyridinic groups and pyridine N-oxide in comparison with the nonpreoxidized samples. The amount of quaternary nitrogen significantly decreased for both melamine-and urea-treated preoxidized samples.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…This can be related to different chemistries of both precursors and formation of large polymers as a result of melamine decomposition by heat treatment. [46] While preoxidation increased the relative amounts of pyrrole/pyridone and pyridinic nitrogen in the melamine derived samples, in ureatreated samples a significant increase was noticed for pyridinic groups and pyridine N-oxide in comparison with the nonpreoxidized samples. The amount of quaternary nitrogen significantly decreased for both melamine-and urea-treated preoxidized samples.…”
Section: Resultsmentioning
confidence: 99%
“…This might be linked to the differences in the chemistries of the interactions of precursors with oxygen-containing surface functional groups and in the mechanisms of their pyrolysis. [46,48] One can hypothesize that less five-member-rings nitrogen groups in S-UO were due to specific interactions of small molecules of urea with oxygen groups via hydrogen bonding, limiting the urea-urea interactions owing to the spatial distance. These interactions could be also responsible for high contents of pyridine-N-oxides and pyridinic nitrogen in these carbons.…”
Section: Resultsmentioning
confidence: 99%
“…In the temperature range starting at 424 °C the resin undergoes extensive degradation. Devallencourt et al [19] assumed that the resin progressively deaminates forming cyameluric structures in the range of 410 °C -525 °C with evaporation of HCN and CH 3 CN. Above 660 °C the MF resin undergoes extensive degradation with production of HCN, CO, CO 2 [19].…”
Section: Characterisation Of the Input Materialsmentioning
confidence: 99%
“…In two partially cured MF resins (microcapsules' shell material) the weight loss did not occur as distinctively on the account of differences in the chemical structure between partially cured and non-cured MF resin. Thermal stability of MF resins was studied in detail by Manley and Higgs [32] and Devallencourt et al [33]. For Melapret NF 70/M the first significant weight loss occurs at the temperature around 160°C, which can be attributed to evaporation of methanol, formaldehyde and water during curing reactions.…”
Section: Thermal Stability Of Microcapsulesmentioning
confidence: 99%
“…At these temperatures ammonia, formaldehyde and other volatile decomposition products are released. The nonvolatile residue contains -NH-bridges between melamine rings as well as different cyameluric structures [33]. In isolated cured MF resins the decrease of weight starts already below 100°C, presumably as a result of adsorbed water on MF resin.…”
Section: Thermal Stability Of Microcapsulesmentioning
confidence: 99%