On Structure and Secondary Linkages in Polymers Based on Glycidyl Azide Polymer and Diisocyanate

Polymers based on glycidyl azide polymer (GAP) and isocyanate present molecular structures dependent on NCO/OH molar ratio and diisocyanate reactivity. In this study, GAP polymers are obtained from a reaction with aromatic (toluene diisocyanate, TDI) or aliphatic (isophoranediisocyanate, IPDI) diis...

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Main Authors: Christiane Bueno Dall´'Agnol, Rita de Cássia Lazzarini Dutra, Milton Faria Diniz, Lucas Sousa Madureira, Silvana Navarro Cassu
Format: Article
Language:English
Published: Instituto de Aeronáutica e Espaço (IAE) 2024-02-01
Series:Journal of Aerospace Technology and Management
Subjects:
Online Access:https://jatm.com.br/jatm/article/view/1321
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author Christiane Bueno Dall´'Agnol
Rita de Cássia Lazzarini Dutra
Milton Faria Diniz
Lucas Sousa Madureira
Silvana Navarro Cassu
author_facet Christiane Bueno Dall´'Agnol
Rita de Cássia Lazzarini Dutra
Milton Faria Diniz
Lucas Sousa Madureira
Silvana Navarro Cassu
author_sort Christiane Bueno Dall´'Agnol
collection DOAJ
description Polymers based on glycidyl azide polymer (GAP) and isocyanate present molecular structures dependent on NCO/OH molar ratio and diisocyanate reactivity. In this study, GAP polymers are obtained from a reaction with aromatic (toluene diisocyanate, TDI) or aliphatic (isophoranediisocyanate, IPDI) diisocyanates, varying the NCO/OH molar ratio from equimolar to 2.5. The increment in NCO/OH molar ratio increases the gel fraction in GAP/TDI polymers up to 90 wt%, along with a progressive growth in their glass transition temperature (Tg), which rises 10 °C from NCO/OH equimolar to 2.5. In opposition, in the GAP/IPDI polymers, the maximum gel fraction is 20 wt%, and the Tg value practically does not change in NCO excess. Infrared spectroscopy shows the predominant presence of urethane groups in polymers containing up to 2.0 NCO/OH molar ratio; however, at 2.5, urethane and allophanate characteristic bands are present in both polymers. That reactivity is controlled by chemical kinetics since the activation barrier of the reaction between the GAP and TDI is 10 kcal.mol‑1 lower than in the corresponding reaction with the IPDI. This difference results from the sum of the higher hyperconjugative interactions, approximately 65%, and the lower steric hindrance, about 35%, in the activated complex containing the TDI.
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spelling doaj.art-5dfad81822b74b78b0a13bbf4f684efc2024-02-19T20:27:03ZengInstituto de Aeronáutica e Espaço (IAE)Journal of Aerospace Technology and Management2175-91462024-02-0116On Structure and Secondary Linkages in Polymers Based on Glycidyl Azide Polymer and DiisocyanateChristiane Bueno Dall´'Agnol 0Rita de Cássia Lazzarini Dutra1Milton Faria Diniz2Lucas Sousa Madureira3Silvana Navarro Cassu4Departamento de Ciência e Tecnologia Aeroespacial – Instituto Tecnológico de Aeronáutica – Programa de Pós-Graduação em Ciências e Tecnologias Espaciais – São José dos Campos/SP – Brazil | Departamento de Ciência e Tecnologia Aeroespacial – Instituto de Aeronáutica e Espaço – Divisão de Propulsão – São José dos Campos/SP – Brazil.Departamento de Ciência e Tecnologia Aeroespacial – Instituto Tecnológico de Aeronáutica – Programa de Pós-Graduação em Ciências e Tecnologias Espaciais – São José dos Campos/SP – Brazil Departamento de Ciência e Tecnologia Aeroespacial – Instituto de Aeronáutica e Espaço – Divisão de Propulsão – São José dos Campos/SP – Brazil.Departamento de Ciência e Tecnologia Aeroespacial – Instituto de Aeronáutica e Espaço – Divisão de Propulsão – São José dos Campos/SP – Brazil.Departamento de Ciência e Tecnologia Aeroespacial – Instituto Tecnológico de Aeronáutica – Programa de Pós-Graduação em Ciências e Tecnologias Espaciais – São José dos Campos/SP – Brazil | Departamento de Ciência e Tecnologia Aeroespacial – Instituto de Aeronáutica e Espaço – Divisão de Propulsão – São José dos Campos/SP – Brazil. Polymers based on glycidyl azide polymer (GAP) and isocyanate present molecular structures dependent on NCO/OH molar ratio and diisocyanate reactivity. In this study, GAP polymers are obtained from a reaction with aromatic (toluene diisocyanate, TDI) or aliphatic (isophoranediisocyanate, IPDI) diisocyanates, varying the NCO/OH molar ratio from equimolar to 2.5. The increment in NCO/OH molar ratio increases the gel fraction in GAP/TDI polymers up to 90 wt%, along with a progressive growth in their glass transition temperature (Tg), which rises 10 °C from NCO/OH equimolar to 2.5. In opposition, in the GAP/IPDI polymers, the maximum gel fraction is 20 wt%, and the Tg value practically does not change in NCO excess. Infrared spectroscopy shows the predominant presence of urethane groups in polymers containing up to 2.0 NCO/OH molar ratio; however, at 2.5, urethane and allophanate characteristic bands are present in both polymers. That reactivity is controlled by chemical kinetics since the activation barrier of the reaction between the GAP and TDI is 10 kcal.mol‑1 lower than in the corresponding reaction with the IPDI. This difference results from the sum of the higher hyperconjugative interactions, approximately 65%, and the lower steric hindrance, about 35%, in the activated complex containing the TDI. https://jatm.com.br/jatm/article/view/1321AllophanateGAPHiperconjugative interaction Steric hindrance
spellingShingle Christiane Bueno Dall´'Agnol
Rita de Cássia Lazzarini Dutra
Milton Faria Diniz
Lucas Sousa Madureira
Silvana Navarro Cassu
On Structure and Secondary Linkages in Polymers Based on Glycidyl Azide Polymer and Diisocyanate
Journal of Aerospace Technology and Management
Allophanate
GAP
Hiperconjugative interaction
Steric hindrance
title On Structure and Secondary Linkages in Polymers Based on Glycidyl Azide Polymer and Diisocyanate
title_full On Structure and Secondary Linkages in Polymers Based on Glycidyl Azide Polymer and Diisocyanate
title_fullStr On Structure and Secondary Linkages in Polymers Based on Glycidyl Azide Polymer and Diisocyanate
title_full_unstemmed On Structure and Secondary Linkages in Polymers Based on Glycidyl Azide Polymer and Diisocyanate
title_short On Structure and Secondary Linkages in Polymers Based on Glycidyl Azide Polymer and Diisocyanate
title_sort on structure and secondary linkages in polymers based on glycidyl azide polymer and diisocyanate
topic Allophanate
GAP
Hiperconjugative interaction
Steric hindrance
url https://jatm.com.br/jatm/article/view/1321
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