Petroleum hydrocabon cracking catalyst and production thereof
A cracking catalyst, petroleum hydrocarbon technology, applied in catalyst activation/preparation, physical/chemical process catalyst, molecular sieve catalyst, etc., can solve problems such as poor isomerization selectivity of straight chain hydrocarbons, reduce olefin content, increase content, improve Effect of Catalytic Performance on Isomerization of Linear Olefins
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Embodiment 1
[0044] The silica modified alumina composition provided by the invention is prepared.
[0045] 500 g deionized water and 506.5 g AlCl 3 ·6H 2 16.1 grams of water glass solution (Shandong Aluminum Factory, SiO 2 content of 20.6%), reacted at room temperature for 30 minutes, then added dropwise 1:1 ammonia water (Beijing Chemical Plant, analytically pure) to adjust the pH value until a gel was formed, and its pH value was 4.5. After continuing to stir and heat up to 65°C , stop stirring and age for 1 hour, vacuum filter. The filter cake was reslurried with decationized water at 60°C for 20 minutes and vacuum filtered. So repeated washing 3 times, to obtain the modified composition M 1 . Its chemical composition, physicochemical properties and surface acidity measured by pyridine adsorption infrared spectroscopy are listed in Table 1.
Embodiment 2
[0047] Preparation of the silica-modified alumina composition provided by the invention.
[0048] 500 g deionized water and 475.2 g AlCl 3 ·6H 2 Slowly add 48.2 grams of water glass solution to the solution of O, react at room temperature for 25 minutes, then add 1:1 ammonia water dropwise to adjust the pH value until a gel is formed, and its pH value is 4.8, continue to stir and heat up to 60°C , stop stirring and age for 1.5 hours, vacuum filter. The filter cake was reslurried with 70°C decationized water for 25 minutes and vacuum filtered. So repeated washing 3 times, to obtain the modified composition M 2 . Its chemical composition, physicochemical properties and surface acidity measured by pyridine adsorption infrared spectroscopy are listed in Table 1.
Embodiment 3
[0050] Preparation of the silica-modified alumina composition provided by the invention.
[0051] 500 grams of deionized water and 454.5 grams of AlCl 3 ·6H 2 Slowly add 69.6 grams of water glass solution to the solution of O, react at room temperature for 30 minutes, then add 1:1 ammonia water dropwise to adjust the pH value until a gel is formed, and its pH value is 5.5, continue to stir and heat up to 70°C , stop stirring and age for 1.5 hours, vacuum filter. The filter cake was reslurried with 65°C decationized water for 30 minutes and then vacuum filtered. So repeated washing 3 times, to obtain the modified composition M 3 . Its chemical composition, physicochemical properties and surface acidity measured by pyridine adsorption infrared spectroscopy are listed in Table 1.
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