화학공학소재연구정보센터
Journal of Physical Chemistry A, Vol.109, No.16, 3550-3557, 2005
Mechanisms and kinetics of noncatalytic ether reaction in supercritical water. 1. Proton-transferred fragmentation of diethyl ether to acetaldehyde in competition with hydrolysis
Noncatalytic reaction pathways and rates of diethyl ether in supercritical water are determined in a quartz capillary by observing the liquid- and gas-phase H-1 and C-13 NMR spectra. The reaction is investigated at two concentrations (0.1 and 0.5 M) in supercritical water at 400 degrees C and over a water-density range of 0.2-0.6 g/cm(3), and in subcritical water at 300 and 350 degrees C. The neat reaction (in the absence of solvent) is also studied for comparison at 0.1 M and 400 degrees C. The ether is found to decompose through (i) the proton-transferred fragmentation to ethane and acetaldehyde and (ii) the hydrolysis to ethanol. Acetaldehyde from reaction (i) is consecutively subjected to the unimolecular and bimolecular redox reactions: (iii) the unimolecular protontransferred decarbonylation forming methane and carbon monoxide, (iv) the bimolecular self-disproportionation producing ethanol and acetic acid, and (v) the bimolecular cross-disproportionation yielding ethanol and carbonic acid. Reactions (ii), (iv), and (v) proceed only in the presence of hot water. Ethanol is produced through the two types of disproportionations and the hydrolysis. The proton-transferred fragmentation is the characteristic reaction at high temperatures and is much more important than the hydrolysis at densities below 0.5 g/cm3. The proton-transferred fragmentation of ether and the decarbonylation of aldehyde are slightly suppressed by the presence of water. The hydrolysis is markedly accelerated by increasing the water density: the rate constant at 400 degrees C is 2.5 x 10(-7) S-1 at 0.2 g/cm(3) and 1.7 x 10(-5) s(-1) at 0.6 g/cm(3). The hydrolysis becomes more important in the ether reaction than the proton-transferred fragmentation at 0.6 g/cm(3). In subcritical water, the hydrolysis path is dominant at 300 degrees C (0.71 g/cm(3)), whereas it becomes less important at 350 degrees C (0.57 g/cm(3)). Acetic acid generated by the self-disproportionation autocatalyzes the hydrolysis at a higher concentration. Thus, the pathway preference can be controlled by the water density, reaction temperature, and initial concentration of diethyl ether.