Method for hydrocarbon preparation through high-grade fatty acid ester hydrogenation
A fatty acid ester, advanced technology, applied in the field of deoxygenation of advanced fatty acid esters to hydrocarbons, can solve the problems of low C-C bond hydrogenolysis cracking activity, low performance of hydrodecarbonylation/hydrodecarboxylation, etc., and achieve the goal of improving decarboxylation selectivity Effect
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Embodiment 1
[0033] CeO 2 The carrier is prepared by the template method, specifically: prepare a 0.1mol / L cetyltrimethylammonium bromide (CTAB) solution, and prepare a certain amount of 0.1mol / L according to n(CTAB) / n(Ce)=0.8 Ce(NO 3 ) 3 ·6H 2 O solution. The CTAB solution was quickly added to the Ce(NO 3 ) 3 ·6H 2 O solution, and stirred rapidly for 20min. At a slightly slower stirring speed, 25% ammonia solution was slowly added dropwise to the above mixed solution until the pH=11, and the stirring was continued for 2 h. The resulting light yellow mixture was placed in a round-bottomed flask, kept in a water bath at 90°C for 4 days, after the mixture was cooled to room temperature, it was suction-filtered, washed alternately with absolute ethanol and distilled water until no Cl was detected in the filtrate. - and NO 3 - ion so far. The cleaned samples were dried in air atmosphere at 120°C for 12h. Then calcined at 500°C for 3h in flowing air to obtain a cerium oxide carrier....
Embodiment 2
[0036] Catalyst preparation process is the same as embodiment 1, and difference is to weigh 2.753 grams of Ni (NO 3 ) 2 ·6H 2 O and 1.089 g NH 4 h 2 PO 4 Made into an aqueous solution, the prepared catalyst is CeO 2 load Ni 2 P Catalyst C-2. Catalyst C-2 was passivated in the same manner as in Example 1 and set aside. The nickel content in catalyst C-2 was 9.6% by weight.
Embodiment 3
[0038] Catalyst preparation process is the same as embodiment 1, difference is weighing 2.753 gram Co(NO 3 ) 2 ·6H 2 O and 1.634 g NH 4 h 2 PO 4 Made into an aqueous solution, the prepared catalyst is CeO 2 Supported CoP catalyst C-3. Catalyst C-3 was passivated in the same manner as in Example 1 and set aside. The cobalt content in catalyst C-3 was 9.7% by weight.
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