Preparation method of hydrocarbon fuel
A hydrocarbon fuel, load-type technology, which is applied in the preparation of liquid hydrocarbon mixtures, chemical instruments and methods, biological raw materials, etc., can solve the problems of increased cost and high reaction temperature
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[0023] The invention discloses a method for preparing hydrocarbon fuel, which comprises the following steps:
[0024] In the presence of hydrogen, the oil and the supported ruthenium-based catalyst are dissolved in an organic solvent, and the oil is subjected to a hydrodeoxygenation reaction in a closed reaction vessel to obtain hydrocarbon fuels. The supported ruthenium-based catalyst is TiO 2 as a catalyst carrier.
[0025] In the present invention, the oil is vegetable oil and / or animal oil, more preferably, one or more selected from the following ingredients: rapeseed oil, rice bran oil, corn oil, soybean oil, sunflower oil, hemp seed oil, Olive oil, coconut oil, peanut oil, mustard oil, cottonseed oil, tallow, lard, whale oil, and fish oil. The main components of the above oils are mixed fatty acid triglycerides, and there are also very small amounts of triglycerides, such as various fat-soluble celluloses (VA, VD, VE and VK), pigments (chlorophyll, carotenoids, etc.) )...
Embodiment 1
[0037] Ruthenium chloride is placed in water, stirred for a certain period of time so that the ruthenium chloride is fully dispersed, and an aqueous ruthenium chloride solution is obtained;
[0038] Calcined pretreated TiO 2 The carrier is impregnated into the ruthenium chloride aqueous solution, fully impregnated at room temperature overnight, then dried at 60°C, and finally calcined in a muffle furnace at 300°C to obtain a supported ruthenium-based catalyst.
Embodiment 2
[0040] Add ethyl stearate and the supported ruthenium-based catalyst prepared by embodiment 1 in the 50ml reactor, the consumption of this loaded ruthenium-based catalyst is 10% of raw material, after dissolving with n-hexane, pour into described reactor 3.0 MPa hydrogen gas was introduced, the reaction temperature was 200° C., the liquid product was obtained after reacting for 17 hours and then cooled to room temperature, and the yield of hydrocarbon fuel was greater than 95%.
[0041] The liquid product prepared by the present embodiment is analyzed by gas chromatography, and the results are as follows: figure 1 As can be seen from the figure, the liquid product is mainly hydrocarbons of C17 and C18, without the peak of ethyl stearate, which proves that the reaction is relatively complete.
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