Journal Article10.1002/APP.20165
Synthesis and degradation behavior of poly(propylene carbonate) derived from carbon dioxide and propylene oxide
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TL;DR: In this paper, the degradation mechanism of poly(propylene carbonate) (PPC) membranes was correlated with the sample morphologies, FTIR, and 1H-NMR spectra.
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Abstract: High molecular weight and regular molecular structure poly(propylene carbonate) (PPC) was successfully synthesized from carbon dioxide and propylene oxide. The PPC copolymer structure was an exact alternating copolymer as evidenced by the 13C-NMR technique. Degradative behavior of the PPC was conducted by soil burial and buffer solution immersion (pH = 6) tests, respectively. The results showed that the weight loss of soil buried in PPC films increased more slowly than that immersed in the buffer solution after 6-month exposure. However, the weight loss of sample immersed in the buffer solution increased rapidly during the first 2 months and reached a value of 4.59%. Water sorption measurement also revealed that the PPC membranes immersed in buffer solution were more hydrophilic than those in soil burial tests. The degradation mechanism of PPC membranes was correlated with the sample morphologies, FTIR, and 1H-NMR spectra. The SEM morphologies were consistent with the weight loss and water sorption measurements. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1840–1846, 2004
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Citations
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A quest for polycarbonates provided via sustainable epoxide/CO2 copolymerization processes
TL;DR: In this article, the authors highlight advances in copolymerization of carbon dioxide and epoxides (oxiranes) to produce polycarbonates, focusing on starting materials that have been generated from renewable feedstocks including straight-chain alkylene oxides, cyclohexadiene oxide, and limonene oxide.
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Functional Polycarbonates from Carbon Dioxide and Tailored Epoxide Monomers: Degradable Materials and Their Application Potential
Abstract: Aliphatic polycarbonates synthesized from carbon dioxide (CO2) and epoxides are resource‐saving, highly biocompatible and biodegradable polymers. Since the discovery of the copolymerization of epoxides and CO2 in 1969 by Inoue et al., this has become an important and useful technology for the large‐scale utilization of CO2 in chemical synthesis, employing mainly propylene oxide, and cyclohexene oxide (CHO). Only in recent years, functionalized polycarbonates have become an emerging topic with a broad scope of potential applications. This review summarizes synthetic routes and properties of numerous functionalized polycarbonates synthesized from CO2 and functional epoxide monomers. Implications for new materials and possible applications, for instance for pharmaceutical purposes and membranes are reviewed. Besides polycarbonates based on oxirane and CHO derivatives, particular emphasis is placed on the manifold synthetic approaches and postpolymerization modifications of glycidyl ether based polycarbonates. Not only functionalized linear polycarbonates are presented but also a variety of novel polycarbonate architectures, e.g., star and hyperbranched polymers.
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Structural characterization and thermal and mechanical properties of poly(propylene carbonate)/MgAl-LDH exfoliation nanocomposite via solution intercalation
TL;DR: In this article, a solution intercalation of polypropylene carbonate (PPC) into the galleries of organic modified double hydroxide (OMgAl-LDH) in cyclohexanone has been studied by Fourier transform infrared spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), selected area electron diffraction, and thermogravimetric analysis.
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