Catalyst for pressurized oxidative coupling of methane to prepare ethylene and its prepn.
An oxidative coupling and catalyst technology, applied in physical/chemical process catalysts, metal/metal oxide/metal hydroxide catalysts, chemical instruments and methods, etc., can solve the problem of increasing reaction pressure, catalytic activity and selectivity decline , unfavorable operation and other problems, to achieve the effect of high content of active components
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Embodiment 1
[0012] Embodiment 1: measure 1ml Mn (NO 3 ) 2 (50%wt), diluted with 20ml of distilled water, heated to 80°C and added to 10.5g of SiO that had been heated to 80°C while stirring 2 , dried at 110°C; weighed 0.53g Na 2 WO 4 Dissolve in 20ml of distilled water, heat to 80°C and add to SiO that has been heated to 80°C while stirring 2 And dry; Weigh 3.38g of dibutyltin dilaurate and dissolve in 20ml of methanol, stir and add to SiO which has been heated to 80°C 2 , baked in an oven at 110°C for 16 hours, transferred to a muffler furnace at 550°C, baked in air for 4 hours, raised the temperature to 850°C and baked for 8 hours to prepare the catalyst. The catalytic performance data of the catalyst are as follows:
[0013] Catalyst Temperature Pressure Methane Stream CH 4 / CH 4 Turn to C 2+ Choose C 2+ receive
[0014] Loading g ℃ MPa Velocity L / h O 2 Conversion rate% Selectivity% Rate%
[0015] 0.4 700 0.6 0.78 4 25.5 60.8 15.5
[0016] 0.4 750 0.6 0.78 4 31.6 71....
Embodiment 2
[0022] Embodiment 2: get 3.0ml Mn (NO 3 ) 2 (50%wt), 1.59g Na 2 WO 4 , diluted with 40ml distilled water, impregnated in 31.5g SiO 2 Above, the method is the same as Example 1. Then use 40ml of toluene solution containing 8.32g dibutyltin dilaurate to impregnate SiO 2 superior. The drying and roasting of the catalyst are the same as in Example 1. Implemented in methane oxidative coupling results are as follows:
[0023] Catalyst Loading Temperature Pressure Methane Flow CH 4 CH 4 C 2+ Choose C 2+ receive
[0024] g ℃ MPa Velocity L / h / O 2 Conversion selectivity %
[0025] Rate% %
[0026] 0.4 730 0.6 0.89 8 20.0 75.5 15.1
Embodiment 3
[0027] Embodiment 3: get 1.0ml Mn (NO 3 ) 2 (50%wt), 0.53g Na 2 WO 4 , diluted with 20ml distilled water, impregnated in 10.5g SiO 2 Above, the method is the same as Example 1. When impregnating the active component Sn, 20ml containing 1.54g SnSO 4 10% methanol in water. The drying and roasting of the catalyst are the same as in Example 1. The evaluation results for methane oxidative coupling are as follows:
[0028] Catalyst Loading Temperature Pressure Methane Flow CH 4 CH 4 C 2+ Choose C 2+ receive
[0029] g ℃ MPa Velocity L / h / O 2 Conversion selectivity %
[0030] Rate% %
[0031] 0.4 720 0.6 1.11 4 30.2 61.3 18.5
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