Understanding the Interactions between Soft Segments in Polyurethanes: Structural Synergies in Blends of Polyester and Polycarbonate Diol Polyols
There are no previous studies on the interactions between polyols of different nature as a model for understanding the interactions between soft segments in PUs. In this study, different blends of two polyols of different natures (polyester—PE, and polycarbonate diol—CD) and similar molecular weight...
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Format: | Article |
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MDPI AG
2023-11-01
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Series: | Polymers |
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Online Access: | https://www.mdpi.com/2073-4360/15/23/4494 |
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author | Yuliet Paez-Amieva José Miguel Martín-Martínez |
author_facet | Yuliet Paez-Amieva José Miguel Martín-Martínez |
author_sort | Yuliet Paez-Amieva |
collection | DOAJ |
description | There are no previous studies on the interactions between polyols of different nature as a model for understanding the interactions between soft segments in PUs. In this study, different blends of two polyols of different natures (polyester—PE, and polycarbonate diol—CD) and similar molecular weights were prepared and their structural, thermal, surface, viscoelastic, and self-adhesion properties were assessed. Different experimental techniques were used: infrared spectroscopy (ATR-IR), differential scanning calorimetry (DSC), X-ray diffraction, thermal gravimetric analysis (TGA), and plate–plate rheology. PE showed a larger number of structural repeating units and a higher number of polar groups than CD, but the carbonate–carbonate interactions in CD were stronger than the ester–ester interactions in PE. The blending of CD and PE imparted synergic structural properties, particularly in the blends containing less than 50 wt.% PE, they were associated with the disrupt of the carbonate–carbonate interactions in CD and the formation of new ester–carbonate and hydroxyl–carbonate interactions. CD + PE blends with less than 50 wt.% PE exhibited higher glass transition temperatures, a new diffraction peak at 2θ = 24°, one additional thermal degradation at 426–436 °C, and a less-steep decline of the storage moduli. Furthermore, the different interactions between the polyol chains in the blends were also evidenced on their surface properties, and all CD + PE blends showed self-adhesion properties which seemed related to the existence of ester–carbonate and carbonate–carbonate interactions. |
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institution | Directory Open Access Journal |
issn | 2073-4360 |
language | English |
last_indexed | 2024-03-09T01:44:33Z |
publishDate | 2023-11-01 |
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series | Polymers |
spelling | doaj.art-f71e2312abfa4dafa50afe3a0383be0b2023-12-08T15:24:11ZengMDPI AGPolymers2073-43602023-11-011523449410.3390/polym15234494Understanding the Interactions between Soft Segments in Polyurethanes: Structural Synergies in Blends of Polyester and Polycarbonate Diol PolyolsYuliet Paez-Amieva0José Miguel Martín-Martínez1Adhesion and Adhesives Laboratory, University of Alicante, 03080 Alicante, SpainAdhesion and Adhesives Laboratory, University of Alicante, 03080 Alicante, SpainThere are no previous studies on the interactions between polyols of different nature as a model for understanding the interactions between soft segments in PUs. In this study, different blends of two polyols of different natures (polyester—PE, and polycarbonate diol—CD) and similar molecular weights were prepared and their structural, thermal, surface, viscoelastic, and self-adhesion properties were assessed. Different experimental techniques were used: infrared spectroscopy (ATR-IR), differential scanning calorimetry (DSC), X-ray diffraction, thermal gravimetric analysis (TGA), and plate–plate rheology. PE showed a larger number of structural repeating units and a higher number of polar groups than CD, but the carbonate–carbonate interactions in CD were stronger than the ester–ester interactions in PE. The blending of CD and PE imparted synergic structural properties, particularly in the blends containing less than 50 wt.% PE, they were associated with the disrupt of the carbonate–carbonate interactions in CD and the formation of new ester–carbonate and hydroxyl–carbonate interactions. CD + PE blends with less than 50 wt.% PE exhibited higher glass transition temperatures, a new diffraction peak at 2θ = 24°, one additional thermal degradation at 426–436 °C, and a less-steep decline of the storage moduli. Furthermore, the different interactions between the polyol chains in the blends were also evidenced on their surface properties, and all CD + PE blends showed self-adhesion properties which seemed related to the existence of ester–carbonate and carbonate–carbonate interactions.https://www.mdpi.com/2073-4360/15/23/4494polyester polyolpolycarbonate diol polyolpolyols blendssoft segmentsester–carbonate interactionsself-adhesion |
spellingShingle | Yuliet Paez-Amieva José Miguel Martín-Martínez Understanding the Interactions between Soft Segments in Polyurethanes: Structural Synergies in Blends of Polyester and Polycarbonate Diol Polyols Polymers polyester polyol polycarbonate diol polyol polyols blends soft segments ester–carbonate interactions self-adhesion |
title | Understanding the Interactions between Soft Segments in Polyurethanes: Structural Synergies in Blends of Polyester and Polycarbonate Diol Polyols |
title_full | Understanding the Interactions between Soft Segments in Polyurethanes: Structural Synergies in Blends of Polyester and Polycarbonate Diol Polyols |
title_fullStr | Understanding the Interactions between Soft Segments in Polyurethanes: Structural Synergies in Blends of Polyester and Polycarbonate Diol Polyols |
title_full_unstemmed | Understanding the Interactions between Soft Segments in Polyurethanes: Structural Synergies in Blends of Polyester and Polycarbonate Diol Polyols |
title_short | Understanding the Interactions between Soft Segments in Polyurethanes: Structural Synergies in Blends of Polyester and Polycarbonate Diol Polyols |
title_sort | understanding the interactions between soft segments in polyurethanes structural synergies in blends of polyester and polycarbonate diol polyols |
topic | polyester polyol polycarbonate diol polyol polyols blends soft segments ester–carbonate interactions self-adhesion |
url | https://www.mdpi.com/2073-4360/15/23/4494 |
work_keys_str_mv | AT yulietpaezamieva understandingtheinteractionsbetweensoftsegmentsinpolyurethanesstructuralsynergiesinblendsofpolyesterandpolycarbonatediolpolyols AT josemiguelmartinmartinez understandingtheinteractionsbetweensoftsegmentsinpolyurethanesstructuralsynergiesinblendsofpolyesterandpolycarbonatediolpolyols |