Method for synthesizing NU-88 molecular sieves
A NU-88 and molecular sieve technology, which is applied in the direction of molecular sieve compounds, molecular sieve characteristic silicates, molecular sieves and alkali exchange compounds, etc., can solve the problems of high cost, energy and material consumption, and large time consumption of double quaternary ammonium salt templates , to achieve the effect of overcoming incomplete reaction of raw materials, avoiding waste and ineffective consumption, and avoiding time consumption
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Embodiment 1
[0067] Under stirring conditions, mix 25.2g of N-methyl-4-piperidone and 23mL of absolute ethanol, and then drop 20g of 1,3-dibromopropane into the above mixture at a rate of 5 drops / second. Pre-reaction at ℃ for 4 hours to obtain the pre-reaction product A1. The molar ratio of 1,3-dibromopropane, N-methyl-4-piperidone and solvent ethanol is 1:2.25:4.07.
[0068] The pre-reaction product A1, 12.086g NaAlO 2 solution, 27.229g of tetraethylammonium hydroxide solution (TEAOH), 10.19g of 30% by weight NaOH solution were dissolved in an appropriate amount of deionized water, mixed evenly, and under stirring conditions, 40g of white carbon black was slowly added to form a milky white colloid The mixture to be crystallized, its molar composition is SiO 2 :Al 2 o 3 : Na 2 O:TEAOH:A1:H 2 O=100:3.3:12:10:15:4000, continue to stir for 1h, transfer to a 1L high-pressure reactor with mechanical stirring, stir and crystallize at 120°C for 2 days, then raise the temperature to 160°C and...
Embodiment 2
[0071]Synthesize NU-88 molecular sieve according to the method of Example 1, the difference is that under stirring conditions, 22.4g of N-methyl-4-piperidone and 32mL of ether were mixed, and then 20g of 1,3-dibromopropane was mixed with 4 drops / Add it dropwise to the above mixed solution at a speed of 2 seconds, and pre-react at 35°C for 12 hours to obtain the pre-reaction product A2. The molar ratio of 1,3-dibromopropane, N-methyl-4-piperidone and solvent ether is 1:2:3.18. The molecular sieve raw powder B2 was obtained by replacing A1 with the pre-reaction product A2. Its XRD spectrum was consistent with that of Example 1. The relative crystallinity and synthesis cost were calculated and listed in Table 1.
Embodiment 3
[0073] Synthesize NU-88 molecular sieve according to the method of Example 1, the difference is that under stirring conditions, 23.52g of N-methyl-4-piperidone was mixed with 27mL of deionized water, and then 20g of 1,3-dibromopropane was mixed with 5 Add it dropwise to the above mixture at a rate of drop / second, and pre-react at 55°C for 48 hours to obtain the pre-reaction product A3. The moles of 1,3-dibromopropane, N-methyl-4-piperidone and solvent water The ratio is 1:2.1:15.5. The molecular sieve raw powder B3 was obtained by replacing A1 with the pre-reaction product A3. Its XRD spectrum was consistent with that of Example 1. The relative crystallinity and synthesis cost were calculated and listed in Table 1.
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