CsPW/Zr-MCM-41 catalyst prepared in supercritical CO2 environment and application of catalyst
A zr-mcm-41, supercritical technology, used in physical/chemical process catalysts, organic compound/hydride/coordination complex catalysts, molecular sieve catalysts, etc. low selectivity issues
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Embodiment 1
[0044] Synthesis of Zr-MCM-41 (Si / Zr=5) carrier: 9.1ml of zirconium n-propoxide and 22.8ml of ethyl orthosilicate were mixed and stirred to obtain mixed system I for later use; 12.2g of hexadecyltrimethyl Dissolve ammonium chloride in 100ml of deionized water, and then mix with 110ml of 28wt% ammonia solution to obtain mixed system II for later use; add mixed system I dropwise to mixed system II under constant stirring, and stir at room temperature for 2 hours at 500r / min After the gel is formed, transfer the mixed system to a polytetrafluoroethylene-lined hydrothermal synthesis kettle, place it in an oven at 80°C for 40 hours, and then cool it to room temperature; filter the mixed solution in the reaction kettle , the solid part was washed 3 times with deionized water, and then the solid was dried in an oven at 80°C for 10 h; the dried solid was baked in a muffle furnace at 450°C for 3 h to obtain Zr-MCM-41 ( Si / Zr=5) carrier.
[0045] Synthesis of 20wt% cesium phosphotungst...
Embodiment 2
[0048] Synthesis of Zr-MCM-41 (Si / Zr=7) carrier: 6.5ml of zirconium n-propoxide and 22.8ml of ethyl orthosilicate were mixed and stirred to obtain mixed system I for later use; 12.2g of hexadecyltriethyl Dissolve ammonium bromide in 110ml of deionized water, and then mix with 110ml of 28wt% ammonia solution to obtain mixed system II for later use; add mixed system I dropwise to mixed system II under constant stirring, and stir at room temperature for 3 hours at 500r / min After the gel was formed, the mixed system was transferred to a polytetrafluoroethylene-lined hydrothermal synthesis kettle, and placed in an oven at 100°C for 45 hours, then cooled to room temperature; the mixed solution in the reaction kettle was filtered , the solid part was washed 4 times with deionized water, and then the solid was dried in a drying oven at 100 °C for 12 h; the dried solid was placed in a muffle furnace at 500 °C for 4 h to prepare Zr-MCM-41 ( Si / Zr=7) carrier.
[0049] Synthesis of 30wt%...
Embodiment 3
[0052] Synthesis of Zr-MCM-41 (Si / Zr=10) carrier: 4.5ml of zirconium n-propoxide and 22.8ml of ethyl orthosilicate were mixed and stirred to obtain mixed system I for later use; then 12.2g of hexadecyl trimethyl Ammonium bromide was dissolved in 100ml of deionized water, and then mixed with 110ml of 28wt% ammonia solution to obtain the mixed system II for later use; under constant stirring, the mixed system I was added dropwise to the mixed system II, and stirred at room temperature at 500r / min After 4 hours until the gel was formed, the mixed system was transferred to a polytetrafluoroethylene-lined hydrothermal synthesis kettle, and placed in an oven at 80°C for 50 hours, then cooled to room temperature; the mixed solution in the reaction kettle was Filter, wash the solid part with deionized water for 5 times, then place the solid in a drying oven at 100°C for 10 hours; place the dried solid in a muffle furnace at 550°C for 5 hours to prepare Zr-MCM-41 (Si / Zr=10) support.
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