Dataset Information

Equilibrium data for the cross-metathesis of methyl oleate with cinnamaldehyde.

ABSTRACT: Here we present equilibrium data for the cross-metathesis of methyl oleate (MO) with cinnamaldehyde (CA) obtained experimentally from liquid-phase catalytic tests conducted at 323?K. The reaction was carried out in batch reactors, using different reactant molar ratios and the 2nd generation Ru Hoveyda-Grubbs complex as catalyst. Reaction mixtures at the equilibrium were analyzed by gas chromatography. Equilibrium constants were determined by assuming unitary activity coefficients for a cinnamaldehyde/methyl oleate equimolar ratio, and the validity of that approximation was evaluated by calculating the equilibrium conversions for different reactant molar ratios.

SUBMITTER: Nieres PD

PROVIDER: S-EPMC6092456 | biostudies-literature | 2018 Oct

REPOSITORIES: biostudies-literature

ACCESS DATA

Publications

Equilibrium data for the cross-metathesis of methyl oleate with cinnamaldehyde.

Nieres Pablo D PD Trasarti Andrés F AF Apesteguía Carlos R CR

Data in brief 20180731

Here we present equilibrium data for the cross-metathesis of methyl oleate (MO) with cinnamaldehyde (CA) obtained experimentally from liquid-phase catalytic tests conducted at 323 K. The reaction was carried out in batch reactors, using different reactant molar ratios and the 2nd generation Ru Hoveyda-Grubbs complex as catalyst. Reaction mixtures at the equilibrium were analyzed by gas chromatography. Equilibrium constants were determined by assuming unitary activity coefficients for a cinnamald ...[more]

PMID: 30112434

Similar Datasets

Project description:The catalytic performance with high conversion and high selectivity of Ti-based oxide catalysts have been widely investigated. Besides, stability, which is an essential parameter in the industrial process, lacked fundamental understanding. In this work, we combined computational and experimental techniques to provide insight into the deactivation of P25 and TS-1 Ti-based oxide catalysts during the methyl oleate (MO) epoxidation. The considered deactivation mechanisms are fouling and surface oxygen vacancy (OV). The fouling causes temporary catalyst deactivation through active site blockage but can be removed via calcination in air at high temperature. However, in this work, the OV formation plays an important role in the overall performance of the spent catalyst as the deactivated catalyst after regeneration, cannot be restored to the initial activity. Also, the effects of OV in spent catalysts caused (i) the formation of more Ti3+ species on the surface as evident by XPS and Bader charge analysis, (ii) the activity modification of the active region on the catalyst surface as the reduction in energy gap (Eg) occurred from the formation of the interstates observed in the density of states profiles of spent catalyst modeled by the O-vacant P25 and TS-1 models. This reduction in Eg affects directly the strength of Ti-OOH active site and MO bonding, in which high binding energy contributes to a low conversion because the MO needed an O atom from Ti-OOH site to form the methyl-9,10-epoxy stearate. Hence, the deactivation of the Ti-based oxide catalysts is caused not only by the insoluble by-products blocking the active region but also mainly from the OV. Note that the design of reactive and stable Ti-based oxide catalysts for MO epoxidation needed strategies to prevent OV formation that permanently deactivated the active region. Thus, the interrelation and magnitude between fouling and OV formation on catalyst deactivation will be investigated in future works.

Dataset Information

Equilibrium data for the cross-metathesis of methyl oleate with cinnamaldehyde.

Publications

Equilibrium data for the cross-metathesis of methyl oleate with cinnamaldehyde.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure