کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
231682 | 1427448 | 2009 | 7 صفحه PDF | دانلود رایگان |
Thermolysis of sulfate turpentine was studied in the pressure range of 40–280 atm. The conversion kinetics of main turpentine components (α-pinene, 3-carene) and their isomerization products (limonene, alloocimenes, pyronenes) was investigated and compared with the conversion kinetics of these compounds in supercritical ethanol. Thermodynamic parameters ΔH¯#, ΔS¯# and ΔG¯# of the reversible reaction “α-pinene-[TS]” were estimated, the observed discrepancies being interpreted in the context of transition state theory. The thermolysis rate of α-pinene as a turpentine component was compared to that in a supercritical diluted solution of ethanol versus pressure. The rate of α-pinene conversion was shown to depend on the density of working medium.
Thermolysis of sulfate turpentine was studied in the pressure range of 40–280 atm. The conversion kinetics of main turpentine components (α-pinene, 3-carene) and their isomerization products (limonene, alloocimenes, pyronenes) was investigated and compared with the conversion kinetics of these compounds in supercritical ethanol. Thermodynamic parameters ΔH¯#, ΔS¯# and ΔG¯# of the reversible reaction “α-pinene-[TS]” were estimated, the observed discrepancies being interpreted in the context of transition state theory. The thermolysis rate of α-pinene as a turpentine component was compared to that in a supercritical diluted solution of ethanol versus pressure. The rate of α-pinene conversion was shown to depend on the density of working medium.Figure optionsDownload as PowerPoint slide
Journal: The Journal of Supercritical Fluids - Volume 48, Issue 2, March 2009, Pages 139–145