| Autor: |
Al Khulaifi RS; Department of Chemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia., AlShehri MM; Department of Chemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia., Al-Owais AA; Department of Chemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia., Algarni TS; Department of Chemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia., Saeed WS; Department of Chemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia., Badjah-Hadj-Ahmed AY; Department of Chemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia., Aouak T; Department of Chemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia. |
| Abstrakt: |
In this work, the isothermal decomposition of poly(methyl methacrylate) synthesized in bulk by the radical route of methyl methacrylate in the presence of azobisisobutyronitrile as the initiator was carried out and monitored for the first time with the DART-Tof-MS technique at different temperatures. Nuclear magnetic resonance (NMR) analysis revealed a predominantly atactic microstructure, and size-exclusion chromatography (SEC) analysis indicated a number average molecular weight of 3 × 10 5 g·mol -1 and a polydispersity index of 2.47 for this polymer. Non-isothermal decomposition of this polymer carried out with thermogravimetry analysis (TGA) showed that the weight loss process occurs in two steps. The first one starts at approximately 224 °C and the second at 320 °C. The isothermal decomposition of this polymer carried out and monitored with the DART-Tof-MS method revealed only one stage of weight loss in this process, which begins at approximately 250 °C, not far from that of the second step observed in the case of the non-isothermal process conducted with the TGA method. The results obtained with the MS part of this technique revealed that the isothermal decomposition of this polymer regenerates a significant part of methyl methacrylate monomer, which increases with temperature. This process involves radical chain reactions leading to homolytic chain scissions and leading to the formation of secondary and tertiary alkyl radicals, mainly regenerating methyl methacrylate monomer through an unzipping rearrangement. Although they are in the minority, other fragments, such as the isomers of 2-methyl carboxyl, 4-methyl, penta-2,4-diene and dimethyl carbate, are also among the products detected. At 200 °C, no trace of monomer was observed, which coincides with the first step of the weight loss observed in the TGA. These compounds are different to those reported by other researchers using TGA coupled with mass spectrometry in which methyl isobutyrate, traces of methyl pyruvate and 2,3-butanonedione were detected. |
