Method for preparing biodiesel by microwave solid alkali ester exchange method
A technology of biodiesel and transesterification, applied in biofuels, fatty acid esterification, chemical instruments and methods, etc., can solve the problems of large consumption of catalyst liquid acid or alkali, inability to resist acid and water, complex post-treatment, etc., to achieve high Promote application value, fast response, and convenient operation
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Embodiment 1
[0017] Process and steps in the present embodiment are as follows:
[0018] (1) design determines that the composition and weight percentage of solid catalyst are:
[0019] Copper Sodium Pyrazine Hydroxyethylene Diphosphonate (Na 2 Cu 3 (Pz)(hedp) 2 (H 2 O) 2 ) 94%
[0020] Sodium Hydroxide (NaOH) 6%
[0021] (2) Dissolve copper nitrate with 10 times the amount of water, add 2 times the amount of hydroxyethylene diphosphonic acid and 1 times the amount of pyrazine, stir and then add 8 times the amount of 1M sodium hydroxide. Seal the mixture into a reaction kettle, react at 150°C for 48 hours, filter and dry to obtain copper sodium pyrazine hydroxyethylene diphosphonate as a solid. Grind and sieve the obtained copper sodium pyrazine hydroxyethylidene diphosphonate solid and soak it in sodium hydroxide solution for 24 hours. The concentration of the sodium hydroxide solution is 0.8 mol / L. Then it was stirred and soaked in deionized water for 8 hours, and then baked at 2...
Embodiment 2
[0025] The processes and steps in this embodiment are exactly the same as those in Embodiment 1 above. The difference is: in step (2), dissolve copper acetate with 10 times the amount of water, add 1 times the amount of hydroxyethylene diphosphonic acid and 1 times the amount of pyrazine, and then add 5 times the amount of 1M hydrogen after stirring. sodium oxide. Seal the mixture into a reaction kettle, react at 150°C for 48 hours, filter and dry to obtain copper sodium pyrazine hydroxyethylene diphosphonate as a solid.
[0026] After the transesterification, a sample was taken for gas chromatography detection, and the measured yield of biodiesel was 92.1%.
Embodiment 3
[0028] The processes and steps in this embodiment are exactly the same as those in Embodiment 2 above. The difference is: in step (2), the baking temperature is 300° C., and the baking time is 5 hours. When the biodiesel was prepared in the (3) step, the microwave output power used for the transesterification reaction was 480W.
[0029] After the transesterification, a sample was taken for gas chromatography detection, and the measured yield of biodiesel was 87.2%.
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