Method for deoxygenation of esters
A technology for esters and ester compounds, applied in the field of hydrodeoxygenation of organic compounds, can solve the problems of combustion deactivation, expensive precious metal catalysts, etc., and achieve the effect of high conversion rate
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Embodiment 1
[0049] Methyl laurate using the aforementioned H 2 S-Fe 3 o 4 Catalyst hydrogenation, under the conditions of 280°C and 320°C, hydrogen pressure of 9MPa, methyl laurate / catalyst ratio of 1 / 2 (weight), reacted for 1 hour. The conversion rate of methyl laurate was analyzed by GC-MS spectrum, and the results are shown in Table 1.
Embodiment 2
[0057] Methyl laurate using H 2 S-Fe 3 o 4 Catalyst hydrogenation, three-factor two-level experiments based on reaction temperature, pressure and time, each with four groups of experiments, hydrogenation conditions: methyl laurate / catalyst = 1 / 2 (weight), catalyst: H 2 S-Fe 3 o 4 , hydrogen environment. Carrying out methyl laurate conversion and product selectivity analysis by GC-MS spectrum (results are shown in Table 2), it can be seen that alkanes are the main products, and the longer the reaction time is, the more favorable the formation of alkanes can be. By prolonging the contact time between the catalyst and the reactants, a higher alkanes yield can be obtained at a lower reaction temperature and pressure.
[0058] Table 2. Methyl laurate conversion rate and hydrogenation product selectivity.
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Embodiment 3
[0066] Octanoic acid methyl ester (C 7 h 15 COOCH 3 ) using H 2 S-Fe 3 o 4 Catalyst hydrogenation, under the conditions of 280°C and 320°C, hydrogen pressure of 9MPa, methyl octanoate / catalyst ratio of 1 / 2 (weight), react for 1 hour. The conversion rate of octanoic acid methyl ester was analyzed by GC-MS spectrum, and the results are shown in Table 4.
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