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Copolymerization of $CO_{2}$, propylene oxide, and itaconic anhydride with double metal cyanide complex catalyst to form crosslinked polypropylene carbonate
| Content Provider | Scilit |
|---|---|
| Author | Luo, Liang Wang, Wen-Zhen Wang, Li Li, Lei-Lei Zhang, Yi-Le Zhao, Sai-Di |
| Copyright Year | 2021 |
| Abstract | In this study, a high-activity Zn–Co double metal cyanide complex was synthesized and used to catalyze the ternary polymerization of carbon dioxide, propylene oxide, and itaconic anhydride to produce a new class of polypropylene carbonates characterized by excellent performance and low ether content. The number average molecular weight of the terpolymer was as high as 2.14 × 105 g·mol−1, and the polydispersity index was as high as 1.58. In the case of PPCIAn3, the 5% weight loss temperature increased by 70°C, the total weight loss temperature increased by 100°C, the tensile strength increased by 6.6 MPa, and the elongation at break decreased to 14.5% with respect to traditional polypropylene carbonate. The apparent efficiency of the catalyst was as high as 45.79 gpolymer/gcatalyst, indicating its high catalytic activity. 1H-NMR spectrometry, gel permeation chromatography, differential scanning calorimetry, thermogravimetric analysis, and in situ Fourier-transform infrared spectroscopy were used to characterize the polymerization process and the structural properties of the obtained terpolymers. |
| Related Links | https://www.degruyter.com/document/doi/10.1515/epoly-2021-0082/pdf |
| Ending Page | 868 |
| Page Count | 15 |
| Starting Page | 854 |
| ISSN | 21974586 |
| e-ISSN | 16187229 |
| DOI | 10.1515/epoly-2021-0082 |
| Journal | e-Polymers |
| Issue Number | 1 |
| Volume Number | 21 |
| Language | English |
| Publisher | Walter de Gruyter GmbH |
| Publisher Date | 2021-01-01 |
| Access Restriction | Open |
| Subject Keyword | E-polymers Ternary Copolymerization Carbon Dioxide Double Metal Cyanide Complex Terpolymerization Green Chemistry Journal: e-Polymers, Vol- 21 |
| Content Type | Text |
| Resource Type | Article |