An examination of the H/D isotope substitution effect on selectivity and activity in the cavitating ultrasound hydrogenation of aqueous 3-buten-2-ol and 1,4-pentadien-3-ol on Pd-black
An H/D isotope effect study of the (H2 versus D2) hydrogenation of the aqueous substrates 3-buten-2-ol (3B2OL) and 1,4-pentadien-3-ol (14PD3OL) was performed using Pd-black catalyst. Either H2O or D2O solvents were employed (for alcohol H/D isotope substitution). Two experimental processing conditions of cavitating ultrasound (CUS) and stirred/silent (SS) methods were used. Products formed include 2-butanol and 2-butanone for the former, and 3-pentanol and 3-pentanone for the latter. The observed selectivity and pseudo-first order reaction rate coefficients (e.g., activity) to these products enabled a mechanistic interpretation of the various reaction conditions to be proposed. Experiments utilized a 50 mL batch reactor maintained at 298 K, employed 5.4 atm of H2 or D2 gas, while seven aliquots were collected during the course of the reaction. We have utilized 1-propanol as an inert dopant in all experiments to enable the rapid onset of cavitation in the CUS systems as described earlier [R.S. Disselkamp et al., J. Catal., 227, 552 (2004)]. The following conclusions were noted. First, the activity of the CUS compared to SS processing were ~100-fold larger. Second, variable catalyst loading experiments for stirred/silent D2 hydrogenation processing indicated that mass transfer of hydrogen gas to the Pd-surface played a role such that higher catalyst loading reduced surface D-atom concentrations and reduced saturated alcohol formation (e.g., via reduced H-addition to surface alkyl radicals). Third, for CUS processing the ketone selectivities for experiments employing water compared to D2O indicated that 3B2OL were twice as large, whereas for 14PD3OL they were comparable. This suggests, somewhat surprisingly, that for 3B2OL enol tautomerization to ketone is a slow, and possibly rate-controlling, process. Finally, again for CUS processing, the similarity in ketone selectivities (all ~17%) for H2 compared to D2 hydrogenation for both 3B2OL and 14PD3OL suggest that both H/D isotopes have rapid surface diffusion and hence give rise to nearly equal selectivies. Restated, the thermal or cavitating ultrasound activation is much greater than the surface H/D diffusion barrier.
- Research Organization:
- Pacific Northwest National Lab. (PNNL), Richland, WA (United States)
- Sponsoring Organization:
- USDOE
- DOE Contract Number:
- AC05-76RL01830
- OSTI ID:
- 884819
- Report Number(s):
- PNNL-SA-46414; IECRED; TRN: US200616%%135
- Journal Information:
- Industrial and Engineering Chemistry Research, 45(11):4015-4018, Vol. 45, Issue 11; ISSN 0888-5885
- Country of Publication:
- United States
- Language:
- English
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