Resistance of polyfluorinated complete esters of polyhydric alcohols to thermal oxidation: Comparison with nonfluorinated analogs
摘要:
Complete esters of pentaerythritol, trimethylolpropane, and 2,2-dimethyl-1,3-propanediol with polyfluorinated carboxylic acids were prepared by esterification. As determined by differential thermal gravimetric analysis in air, the resistance of the esters to thermal oxidation decreases in going from pentaerythritol derivatives to those of trimethylolpropane and then to those of 2,2-dimethyl-1,3-propanediol. The compounds synthesized surpass their nonfluorinated analogs in the resistance to thermal oxidation.
Synthesis and GC-MS study of fluorinated esters derived from thrimethylolpropane
作者:M. G. Pervova、V. E. Kirichenko、T. I. Gorbunova、A. Ya. Zapevalov、V. I. Saloutin
DOI:10.1134/s1070363208090107
日期:2008.9
Zol-gel process was used to synthesize equilibrium mixtures of mono-, di-, and trimester derived from trimethylolpropane and perfluorocarboxylic acids. The elution order of the components of the mixtures from a weakly polar HP-5 column was established. The mass spectra of the synthesized compounds were studied. The GC-MS parameters of the products were compared with the respective parameters of their nonfluorinated analogs. The characteristics of the fluorinated esters have features determined by the esterification degree and the nature of the perfluoroalkyl groups, due to which these compounds can be identified in mixtures.
Resistance of polyfluorinated complete esters of polyhydric alcohols to thermal oxidation: Comparison with nonfluorinated analogs
作者:T. I. Gorbunova、S. M. Sorokina、A. Ya. Zapevalov、V. I. Saloutin
DOI:10.1134/s1070363206110223
日期:2006.11
Complete esters of pentaerythritol, trimethylolpropane, and 2,2-dimethyl-1,3-propanediol with polyfluorinated carboxylic acids were prepared by esterification. As determined by differential thermal gravimetric analysis in air, the resistance of the esters to thermal oxidation decreases in going from pentaerythritol derivatives to those of trimethylolpropane and then to those of 2,2-dimethyl-1,3-propanediol. The compounds synthesized surpass their nonfluorinated analogs in the resistance to thermal oxidation.