Method for synthesizing CoAPO-41 molecular sieve
A technology of coapo-41 and molecular sieve, which is applied in the direction of molecular sieve compounds, molecular sieve characteristic aluminum phosphate, molecular sieve and alkali-exchanged phosphate, etc., can solve the problem of orifice or channel blockage, shorten the crystallization time, and inhibit carbon deposition and deactivation , Mild and acidic effect
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specific Embodiment approach 1
[0023] Specific embodiment one: a kind of method for synthesizing CoAPO-41 molecular sieve described in this embodiment is specifically carried out according to the following steps:
[0024] 1. Preparation of initial gel: Weigh 85% phosphoric acid, secondary deionized water, pseudoboehmite, di-n-butylamine and cobalt nitrate by weighing 85% phosphoric acid Mix evenly with secondary deionized water to obtain a reaction system. Under the stirring condition of a rotating speed of 800r / min~1000r / min, add pseudo-boehmite, di-n-butylamine and cobalt nitrate to the reaction system in sequence, and stir for 20min ~40min to get the initial gel;
[0025] The mass ratio of 85% phosphoric acid to secondary deionized water is 1:(3.5~4.5); the mass percentage is the mass of 85% phosphoric acid and pseudo-boehmite The ratio is 1:(0.5~0.7); the mass ratio of phosphoric acid and di-n-butylamine in the described mass percentage is 1:(1.5~2.0); the described mass percentage is 85% The mass rat...
specific Embodiment approach 2
[0030] Specific embodiment two: the difference between this embodiment and specific embodiment one is: Al in the pseudo-boehmite described in step one 2 o 3 The mass percent composition of cobalt nitrate described in step one is 71.3%; The mass percent composition of cobalt nitrate described in step one is 99%; The mass percent composition of di-n-butylamine described in step one is 99%. Others are the same as in the first embodiment.
specific Embodiment approach 3
[0031] Embodiment 3: This embodiment is different from Embodiment 1 or Embodiment 2 in that: in step 2, the crystallization is carried out at a temperature of 170° C. to 190° C. for 12 hours to 24 hours. Others are the same as in the first or second embodiment.
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