Tuning alkylation reactions with temperature in near-critical water
β Scribed by Karen Chandler; Charles L. Liotta; Charles A. Eckert; David Schiraldi
- Publisher
- American Institute of Chemical Engineers
- Year
- 1998
- Tongue
- English
- Weight
- 754 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0001-1541
No coin nor oath required. For personal study only.
β¦ Synopsis
Quantitative kinetics for the alkylation reactions of phenol and p-cresol with tert-butyl alcohol in near-critical water as a function of temperature are reported. The reaction products of the alkylation reactions were ortho-and para-substituted phenols, which are used extensively as antioxidants in numerous polymer systems. A new experimental reaction apparatus was designed, constructed, and successfilly operated to allow pressure control and sampling of the reaction .lystems, which provided rate constants in the temperature range 250 -300Β°C. Additionally, activation energies and heats of formation were calculated fvom the temperature dependence of the rate constants, and orthosubstitution was found to be exothermic whereas para-substitution was found to be endothermic. These results demonstrate that product distribution of the alkylation reactions could be tuned with temperature to produce specific products.
π SIMILAR VOLUMES
Due to mode coupling, the fluctuations in near-critical liquids with temperature gradients differ from equilibrium ones at Ε½ . length-scales r ) r . The mode coupling radius r decreases when the reduced temperature Β΄s T y T rT decreases at mc mc c c Ε½ . a constant temperature gradient, and may coin
## Abstract Aromatic amines were prepared in good yields by a novel reduction of aromatic nitro compounds with tellurium metal in nearβcritical water at 275Β°C.