Process method for preparing ethyl tert-butyl ether
A technology of ethyl tertiary butyl ether and process method, which is applied in the directions of adding unsaturated compounds to prepare ether, ether preparation, chemical instruments and methods, etc., can solve the problems of reduced activity, loss of dissolution, poor stability, etc. High, easy to operate, good stability
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preparation example Construction
[0026] In the preparation process of the above-mentioned titanium-based composite oxide, the reaction time is 3h-24h, preferably 5h-20h, and most preferably 6h-12h. The drying temperature is 100°C to 180°C, preferably 100°C to 160°C, and most preferably 100°C to 120°C. The drying time is 8h-24h, preferably 6h-16h, most preferably 8h-12h. The calcination temperature is 400°C to 600°C, preferably 400°C to 550°C, and most preferably 400°C to 500°C. The roasting time is 8h-24h, preferably 8h-20h, most preferably 8h-16h.
[0027] The formed titanium-based composite oxide support is impregnated in a heteropolyacid solution according to a conventional impregnation method. The immersion time is 6h-24h, preferably 6h-16h, most preferably 8h-12h. The impregnated product is dried at 100°C~160°C for 6h~12h, preferably at 100°C~140°C for 6h~10h, most preferably at 100°C~120°C for 8h~10h. The impregnated product is roasted at 350℃~650℃ for 8h~24h, preferably at 400℃~550℃ for 8h~16h, mos...
Embodiment 1
[0030] A certain amount of aluminum nitrate and a certain amount of titanium tetrachloride are prepared into aqueous solution a, potassium hydroxide alkaline solution b is prepared, and solution b is added dropwise to a under normal temperature and stirring, and the reaction is 10h to obtain a white paste After washing, filtering, drying at 120°C for 10h, extruding into strips according to conventional methods, and then calcining at 500°C for 8h to obtain a titanium-based composite oxide carrier.
[0031] A certain amount of phosphomolybdic acid was dissolved in deionized water, and the above shaped and calcined catalyst carrier was immersed in the heteropoly solution for 8 hours. The catalyst was obtained, and the physical properties of the catalyst are shown in Table 1.
[0032] The etherification of isobutene and ethanol was carried out in a stainless steel fixed-bed reactor of Φ18mm×1200mm, and 30ml of the above-mentioned catalyst was loaded into the reactor. The top and b...
Embodiment 2
[0034] Other conditions are the same as in Example 1, except that the consumption of aluminum nitrate and phosphomolybdic acid is changed, the catalyst composition is shown in Table 1, and the reaction result is shown in Table 2.
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