Reference of 453-20-3, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.453-20-3, Name is 3-Hydroxytetrahydrofuran, molecular formula is C4H8O2. In a article£¬once mentioned of 453-20-3
Vapor-phase reaction of polyols over copper catalysts
The vapor-phase reaction of triols and diols was performed over copper metal catalysts. Triols, such as 1,2,3-propanetriol (glycerol) and 1,2,3- and 1,2,4-butanetriols, were dehydrated to afford corresponding hydroxyketones, while 1,2-propanediol was dehydrogenated to form hydroxyacetone. Supported copper as well as pure copper metal was an effective catalyst for the dehydration of glycerol to produce hydroxyacetone under inert conditions. In hydrogen flow, however, copper catalyzed the hydrogenation of hydroxyacetone as well as hydrogenolysis to produce ethylene glycol. Alumina-supported copper showed the highest catalytic activity with hydroxyacetone selectivity of >90 mol% at ambient pressure of nitrogen and 250 C. Copper metal provides an active site for the dehydration of glycerol. We propose a reaction mechanism for the dehydration of glycerol to form hydroxyacetone.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 453-20-3
Reference£º
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem