Device and method for preparing single-walled carbon nanotubes through extensible floating catalytic cracking
A single-walled carbon nanotube, floating catalytic cracking technology, applied in the fields of carbon nanotubes, chemical instruments and methods, nanocarbons, etc., can solve the problem of difficult to break through the daily production capacity of kilogram-scale single-walled carbon nanotubes, and uncontrollable product collection continuity. and other problems to achieve the effect of maintaining uniformity and reducing load
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Embodiment 1
[0082] The carrier gas was preheated to 280 °C to open the catalyst pretreatment unit, and the temperature of the product synthesis unit was raised to 900 °C; then, ferrocene was injected into the catalyst pretreatment unit with a total volume of 0.5L through the powder feeder, and the catalyst auxiliary thiophene was injected at the same time. The preheated carrier gas is mixed with catalyst and catalyst assistant and sent to the catalyst pretreatment unit, wherein the iron / sulfur molar ratio in the catalyst and catalyst assistant is controlled to be 1:8. The carbon source mixed gas is introduced into the reaction chamber with a volume of 25L to carry out the synthesis reaction. The generated product enters the product collection unit with the gas through the connecting pipeline, and the final product is obtained by filtration and separation.
[0083] The carbon source mixed gas comprises carbon source gas 10% methane, the reducing gas volume is 32% hydrogen and 2% water vapor...
Embodiment 2
[0087] The difference between the device and the process method in Example 1 is that the carrier gas is preheated to 400°C, and the product synthesis unit is heated to 1170°C;
[0088] The total volume of the catalyst pretreatment unit is 8L, and the volume of the reaction chamber is 400L;
[0089] The product collection unit obtains the final product by moving the scraper.
[0090] The carbon source mixed gas comprises carbon source gas 12% methane, reducing gas 35% hydrogen and 5% carbon monoxide mixed gas, water vapor is 3%, and the rest is nitrogen inert gas. The carbon source mixture is preheated to 430°C.
[0091] The included angle of the accelerating monomers of the catalyst pretreatment unit adopts three sets of equal ratios of 1:2:3 combined accelerating units to be nested in a non-closed conical structure, the included angles are 5, 10, and 15 degrees respectively, and the distance is 15mm. Using tungsten high temperature resistant material, the gas velocity at t...
Embodiment 3
[0094] The difference between the device and the process method of Example 2 is that the carrier gas is preheated to 660°C and the product synthesis unit is heated to 1370°C;
[0095] The total volume of the catalyst pretreatment unit is 18L, and the volume of the reaction chamber is 2000L;
[0096] Described iron / sulfur ratio is controlled to be 1:5;
[0097] The collection unit obtains the final product by means of cyclone separation.
[0098] The carbon source mixed gas comprises carbon source gas 15% methane, reducing gas 50% hydrogen, water vapor 5%, and the rest is nitrogen inert gas. The carbon source mixture is preheated to 480°C.
[0099] The included angle of the accelerating monomers of the catalyst pretreatment unit adopts 6 groups of equal ratios of 1:2:3 combined accelerating units to be nested in a non-closed conical structure, the included angles are 10, 20, and 30 degrees respectively, and the distance is 45mm. Using graphite high temperature resistant mat...
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