التفاصيل البيبلوغرافية
| العنوان: |
Solvent effect in H-BEA catalyzed cyclohexanol dehydration reaction. |
| المؤلفون: |
Li, Sha, Chen, Huimin |
| المصدر: |
Journal of Chemical Physics; 6/21/2024, Vol. 160 Issue 23, p1-6, 6p |
| مصطلحات موضوعية: |
DEHYDRATION reactions, SOLVENTS, MOLECULAR dynamics, BRONSTED acids, DIOXANE, UNIT cell |
| مستخلص: |
The solvent effect on H-BEA catalyzed cyclohexanol dehydration was investigated in water, dioxane, and cyclohexanol. The dynamic evolution of the Brønsted acid site of zeolite and its interaction with reactant molecules in different solvents were explored with ab initio molecular dynamics simulations, providing reliable configuration sampling to obtain configurations at equilibrium. Solvent profoundly changes the adsorption as well as the dehydration reaction of cyclohexanol in H-BEA, where the reaction is determined to follow the E2 mechanism in water and dioxane but the E1 mechanism in cyclohexanol untill saturation uptake. Near saturation uptake, all three solvents significantly reduce the cyclohexanol dehydration rates in H-BEA. Cyclohexanol loading also dramatically affects the kinetics of the dehydration reaction, displaying an overall decreasing trend with a local minimum present at intermediate loading of 6 molecules per unit cell, which is a result of the entropic effect associated with greater freedom of motion of the transition state. Rigorous quantification of enthalpy and entropy contributions to cyclohexanol adsorption and activation shed light on the solvent effect of zeolite-catalyzed alcohol dehydration. [ABSTRACT FROM AUTHOR] |
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| قاعدة البيانات: |
Complementary Index |
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