Thermal decomposition characteristics of poly[diethyl‐2‐(methacryloyloxy)ethyl phosphate] using thermogravimetric analysis/mass spectrometry

Abstract

Abstract The thermal decomposition of poly[diethyl 2‐(methacryloyloxy)ethyl phosphate] (PDMP) by free‐radical polymerization was studied by the combination of pyrolysis‐gas chromatography/mass spectrometry (Py‐GC/MS) with thermogravimetric analysis/mass spectrometry (TG/MS), in which the former identified directly the compositions of the evolved gases and the latter could further obtain real‐time evolution curves of pyrolysates. A decomposition of PDMP was a two‐stage process: The dominant mechanism of the first stage was initialized by hydrolysis at the phosphate ester linkage to evolve hydroxyethyl methacrylate (HEMA), triethylphosphate, and ethanol as major products; then, subsequently, the dominant mechanism of the second stage was a main‐chain random scission to form acetaldehyde and water as major products along with carbonization of about 24% char yield of a solid residue at 600°C. Therefore, the reaction of phosphate groups into the backbone of polymeric materials could provide better flame retardancy. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 821–830, 2002