2023
DOI: 10.1039/d2ra05710g
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Biodegradable isocyanate-free polyurethane films via a noncatalytic route: facile modified polycaprolactone triol and biobased diamine as precursors

Abstract: Synthesis of isocyanate free polyurethanes was executed via catalyst free condition by polyaddition of biodegradable cyclic carbonate from polycaprolactone triol and sustainable diamines formed from linalool and isosorbide diamine by chemical approach.

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Cited by 6 publications
(8 citation statements)
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“…From Figure b, the aminolysis of polyurethane is confirmed by the induced smooth broad peak at 22.5°, and sharp crystalline peaks at 21.9 and 23.9° confirm the perfect blending of PCL. The PU and PU/PCL films confirm the amorphous nature of polyurethane at 20.4° as a broad valley; after the modification with PCL, the amorphous nature of PU changed into semicrystalline at 21.9 and 23.5°, as shown in Figure S2, due to the presence of PCL. Thus, the XRD analysis proves that the material has not undergone a complete loss of its nature; rather, there is clear evidence of a slight shift in its crystalline nature.…”
Section: Resultsmentioning
confidence: 65%
“…From Figure b, the aminolysis of polyurethane is confirmed by the induced smooth broad peak at 22.5°, and sharp crystalline peaks at 21.9 and 23.9° confirm the perfect blending of PCL. The PU and PU/PCL films confirm the amorphous nature of polyurethane at 20.4° as a broad valley; after the modification with PCL, the amorphous nature of PU changed into semicrystalline at 21.9 and 23.5°, as shown in Figure S2, due to the presence of PCL. Thus, the XRD analysis proves that the material has not undergone a complete loss of its nature; rather, there is clear evidence of a slight shift in its crystalline nature.…”
Section: Resultsmentioning
confidence: 65%
“…Furthermore, the XRD patterns of the crafted PBU, showcased in Figure 2d, mirror the diffraction patterns frequently seen in other urethane-based polymer films, predominantly characterized by a singular, expansive peak around 2θ = 20°. 36 The DA reaction emerges as a cornerstone in the curing mechanism of PBU within the scope of this research. As elucidated in Figure 2e, the DA reaction, in essence, represents a cycloaddition process.…”
Section: ■ Results and Discussionmentioning
confidence: 98%
“…Diving into the C 1s XPS spectrum deconvolution for the PBU, peaks indicative of C–C, C–H, and C–O bonds manifest at 285.28 and 286.5 eV, aligning harmoniously with the observations from the FT-IR spectra (as seen in Figure c). Furthermore, the XRD patterns of the crafted PBU, showcased in Figure d, mirror the diffraction patterns frequently seen in other urethane-based polymer films, predominantly characterized by a singular, expansive peak around 2θ = 20° . The DA reaction emerges as a cornerstone in the curing mechanism of PBU within the scope of this research.…”
Section: Resultsmentioning
confidence: 99%
“…[156] We have recently reported the isocyanate and catalyst free one-pot synthesis of biodegradable NIPU films by polyaddition of cyclic carbonate of polycaprolactone triol with biodegradable/sustainable diamines, hexamethylene diamine/isosorbide diamine and terpene-based linalool diamine to form NIPU films as represented in Scheme 70. [171]…”
Section: Chemistryselectmentioning
confidence: 99%