A kind of method of 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] 50 g of hydrogen-type mordenite with a silicon-aluminum ratio of 4:1 was calcined at 550° C. for 5 hours in an air atmosphere in a muffle furnace, and a part of the powder samples were pressed into tablets and crushed into 20-40 meshes for activity testing. Weigh 10 g of the hydrogen-type mordenite sample, put it into a stainless steel reaction tube with an inner diameter of 8.5 mm, activate it with nitrogen gas at normal pressure and 300 °C for 1 hour, and then bubble it with nitrogen gas liquid, will Blow into hydrogen-type mordenite, treat for 2 hours, and then blow with nitrogen for 1 hour, then drop to 250 ° C, pass through carbon monoxide: dimethyl ether: Slowly increase the pressure to the reaction pressure of 2MPa, control the reaction space velocity GHSV=1000h -1 , using gas chromatography to detect and analyze the tail gas online, and calculate the conversion rate of dimethyl ether and the selectivity of methyl acetate. The reaction results are shown in Ta...
Embodiment 2
[0042] The experimental procedure is the same as in Example 1, the silicon-alumina ratio of the hydrogen-type mordenite is changed to 6: 1, and the pre-absorbed alicyclic organic amine on the catalyst is changed to The alicyclic organic amine in the feed gas is replaced by The rest of the 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-type mordenite is changed to 60: 1, and the pre-absorbed alicyclic organic amine on the catalyst is changed to The alicyclic organic amine in the feed gas is replaced by the molar ratio of 1:1 The rest of the experimental steps are consistent with Example 1, and the reaction results are shown in Table 1.
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