Gas chromatographic determination of pyrolysis products from poly(2-hydroxyethyl methacrylate)

Perovskite Pattern Formation by Chemical Vapor Deposition Using Photolithographically Defined Templates

“…However, further degradation of the copolymer film results in the formation of other functional groups for effective nucleation at 255 °C, in which complicated degradation mechanisms can be involved to form a variety of functional groups. 43,44 Figure 3e further confirms that the 235 °C condition is a "sweet-spot" for selective PbI 2 deposition. PbI 2 domains were not observed in the PGN square, where the symmetric distributions from the center were discovered from the other temperature conditions, due to the surface diffusion of adsorbed species from PGN to Si.…”

Effects of pH, ionic strength, and applied voltage on migration of dental monomers in an organic matrix

“…Neither BisGMA nor TEGDMA showed an electromigration and HEMA showed a small amount of electromigration. When HEMA degrades, it splits into methacrylic acid and ethylene glycol [34]. The highly mobile acidic species in the HEMA lane may be due to small amounts of methacrylic acid.…”

Effect of the crosslinking degree and the nickel salt load on the thermal decomposition of poly(2-hydroxyethyl methacrylate) hydrogels and on the metal release from them

“…In this case, the degradation products are of low molecular weight and their composition depends on the chemical structure of the side chain of the polymer [23][24][25][26][27]. When the side chain of the polymer is hydrophilic the formation of cyclic anhydrides is prevented, this is the case of PHEMA polymers [22,28]. The thermal degradation studies of PHEMA by pyrolysis [29] showed that the main degradation products were 2-hydroxyethyl methacrylate (HEMA) and ethylene dimethacrylate (EDMA).…”