Method used for producing methyl acetate
A technology of methyl acetate and dimethyl ether, which is applied in the field of preparing methyl acetate through carbonylation of dimethyl ether, can solve the problems of short life, poor catalyst stability, and restricted application, and achieve the effect of prolonging life and improving stability
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Embodiment 1
[0040] 50g of hydrogen-type mordenite with a silicon-to-aluminum ratio of 4:1 was calcined at 550°C in an air atmosphere of a muffle furnace for 5 hours, and a part of the powder samples were taken into tablets and crushed into 20-40 meshes for activity testing. Weigh 10g of the hydrogen-type mordenite sample, put it into a stainless steel reaction tube with an inner diameter of 8.5mm, activate it with nitrogen at normal pressure and 300°C for 1 hour, and then bubbling with nitrogen Liquid, will Blow into the hydrogen-type mordenite, treat for 2 hours, then purge with nitrogen for 1 hour, then drop to 250°C, and pass in carbon monoxide: dimethyl ether: Slowly increase the pressure to the reaction pressure of 2MPa, control the reaction space velocity GHSV=1000h -1 , Use gas chromatography to detect and analyze the tail gas online, calculate the conversion rate of dimethyl ether and the selectivity of methyl acetate, the reaction results are shown in Table 1.
Embodiment 2
[0042] The experimental procedure is the same as in Example 1. The silicon-to-alumina ratio of the hydrogen mordenite is changed to 6:1, and the alicyclic organic amine pre-adsorbed on the catalyst is changed to Alicyclic organic amine in the feed gas is replaced by The remaining experimental steps are consistent with Example 1, and the reaction results are shown in Table 1.
Embodiment 3
[0044] The experimental procedure is the same as in Example 1. The silicon-aluminum ratio of the hydrogen mordenite is changed to 60:1, and the alicyclic organic amine pre-adsorbed on the catalyst is changed to The alicyclic organic amine in the feed gas is replaced with a molar ratio of 1:1 The remaining experimental steps are consistent with Example 1, and the reaction results are shown in Table 1.
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