Development of heterogeneous acid catalysts produced from the carbonization ofMiscanthusxgiganteusfor the esterification of butyric acid to butyl butyrate with n-butanol

2015 ◽  
Vol 91 (7) ◽  
pp. 2076-2084 ◽  
Author(s):  
Francesco Severini ◽  
Thomas Flannelly ◽  
Daniel O' Nolan ◽  
James J Leahy ◽  
Witold Kwapinski
Author(s):  
F. N. Bedretdinov ◽  
T. V. Chelyuskina

In the present work, an analysis of the mutual arrangement of a number of iso-manifolds in the concentration tetrahedron formed by the components of the separated mixture and an additional substance, an extractive agent, was carried out to estimate the possibility of separating three-component mixtures containing biazeotropic constituents by extractive rectification. The objects of research were four-component systems formed by ternary constituents (butyl propionate (BP) - propionic acid (PA) - butyl butyrate (BB), butyl propionate - propionic acid - butyric acid (BA), butyl butyrate - butyric acid -butyl propionate, butyl butyrate - butyric acid -propionic acid) of the commercially important BP-PA-BB-BA system, and the extractive agent sulfolane. Using the results of the computational experiment based on mathematical model NRTL-HOC we obtained complete data on the vapor-liquid equilibrium in binary, three- and four-component systems. The structures of liquid-vapor phase diagrams were obtained, and thermodynamic-topological analysis of all four-component systems was carried out. The mutual arrangement in the concentration tetrahedron of manifolds of relative volatility (equal to 1) of the components, reflecting the evolution of pseudo-azeotropes in sections with a constant concentration of the extractive agent; pseudo-ideal manifolds along which the activity coefficients of the components of the base (separated) mixture are equal to each other; isothermo-isobaric manifolds generated by Bancroft points in binary azeotropic constituents were determined. We established that it is possible to separate the studied three-component mixtures by extractive rectification using sulfolane.


2013 ◽  
Vol 130 ◽  
pp. 793-797 ◽  
Author(s):  
Venkata K.S. Pappu ◽  
Victor Kanyi ◽  
Arati Santhanakrishnan ◽  
Carl T. Lira ◽  
Dennis J. Miller

Author(s):  
Alex L. Bagdasarian ◽  
Stasik Popov ◽  
Benjamin Wigman ◽  
Wenjing Wei ◽  
woojin lee ◽  
...  

Herein we report the 3,5bistrifluoromethylphenyl urea-catalyzed functionalization of unactivated C–H bonds. In this system, the urea catalyst mediates the formation of high-energy vinyl carbocations that undergo facile C–H insertion and Friedel–Crafts reactions. We introduce a new paradigm for these privileged scaffolds where the combination of hydrogen bonding motifs and strong bases affords highly active Lewis acid catalysts capable of ionizing strong C–O bonds. Despite the highly Lewis acidic nature of these catalysts that enables triflate abstraction from sp<sup>2</sup> carbons, these newly found reaction conditions allow for the formation of heterocycles and tolerate highly Lewis basic heteroaromatic substrates. This strategy showcases the potential utility of dicoordinated vinyl carbocations in organic synthesis.<br>


2020 ◽  
Author(s):  
Alex L. Bagdasarian ◽  
Stasik Popov ◽  
Benjamin Wigman ◽  
Wenjing Wei ◽  
woojin lee ◽  
...  

Herein we report the 3,5bistrifluoromethylphenyl urea-catalyzed functionalization of unactivated C–H bonds. In this system, the urea catalyst mediates the formation of high-energy vinyl carbocations that undergo facile C–H insertion and Friedel–Crafts reactions. We introduce a new paradigm for these privileged scaffolds where the combination of hydrogen bonding motifs and strong bases affords highly active Lewis acid catalysts capable of ionizing strong C–O bonds. Despite the highly Lewis acidic nature of these catalysts that enables triflate abstraction from sp<sup>2</sup> carbons, these newly found reaction conditions allow for the formation of heterocycles and tolerate highly Lewis basic heteroaromatic substrates. This strategy showcases the potential utility of dicoordinated vinyl carbocations in organic synthesis.<br>


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