SCHEDULED MAINTENANCE
Kinetics and adsorption calculations: insights into the MgO-catalyzed detoxification of simulants of organophosphorus biocides†
*ab
Eduardo H.
Wanderlind,
*cd
Felipe S. S.
Schneider,
c
Giovanni F.
Caramori,
c
Renato L. T.
Parreira,
e
Abstract
We report the targeted decomposition of the organophosphate methyl paraoxon by means of its transesterification with 1-propanol catalyzed by magnesium oxide. Catalyst characterization by energy dispersive X-ray fluorescence (EDXRF), nitrogen adsorption/desorption measurements (BET and BJH methods), and temperature programmed desorption of CO2 (CO2-TPD) showed that the employed MgO presents properties favorable for the methyl paraoxon adsorption and transesterification to occur. A thorough kinetic investigation showed that rate enhancements up to 3 × 106-fold can be achieved in comparison with the spontaneous propanolysis of the substrate, and that the material can be used in additional cycles without loss of catalytic activity, with the catalyst recovery achieved through a simple washing procedure. Energies for adsorption of 1-propanol and methyl paraoxon onto a MgO model surface were obtained by density functional theory calculations, which showed that the latter displays a stronger affinity for the catalyst surface, and that the reaction should proceed with methyl paraoxon and 1-propanol molecules juxtapositioned at adjacent Mg2+ sites, with nucleophilic and electrophilic centers ca. 2.4 Å away from each other. Additionally, MgO also promoted rate enhancements up to 5 × 104-fold in the propanolysis of a further range of representative phosphate triesters, and in most of the cases the final transesterified products are trialkyl phosphates structurally related to a family of flame-retardants. The results thus provide insights into the development of novel systems for the targeted conversion of organophosphorus compounds into value-added products by employing simple, highly efficient, and low-cost metal oxide catalysts.
Please wait while we load your content...
