Method for preparing biodiesel and co-producing triacetin
A technology of glycerol acetate and biodiesel, which is applied in the direction of biofuel, carboxylic acid ester preparation, fatty acid esterification, etc., can solve the problems that do not involve the co-production and utilization of glycerol, a by-product of transesterification, and achieve unique catalytic characteristics and catalytic performance Stable, easy-to-separate effect
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Embodiment 1
[0017] Embodiment 1: 100g high acid value grease (acid value 2.0mgKOH / g), 22.9g methanol and 2.0g ionic liquid (3-sulfonic acid) propyltriethylammonium chloride zincate (wherein 3-sulfonic acid chloride The molar ratio of acid propyltriethylammonium salt to zinc chloride is 1:3), added into the autoclave, heated and stirred, and reacted at 50°C for 12h. After static cooling, the mixture was taken out and allowed to stand for layering and phase separation. The upper layer of biodiesel was neutralized, washed with water and dehydrated to obtain 99.0 g of biodiesel (98.5% yield). The residue obtained after removing methanol and water from the ionic liquid phase of the lower layer is 1: 3.5 according to the molar ratio of glycerin and acetic acid. The by-product acetic acid is reclaimed under pressure, and the gained residue is left to separate phases. The upper strata is glycerol triacetate, and the lower floor is an ionic liquid phase. The yield is 98.0%), and the ionic liquid ...
Embodiment 2
[0019] Embodiment 2: 100g high acid value grease (acid value 15.0mgKOH / g), 69.1g methyl alcohol and 10.0g ionic liquid (3-sulfonic acid) propyltriethylammonium chloroferrate (wherein 3-sulfonic acid chloride The molar ratio of acid propyltriethylammonium salt to ferric chloride is 1:3), added into the autoclave, heated and stirred, and reacted at 140°C for 6h. After static cooling, the mixture was taken out and allowed to stand for layering and phase separation. The biodiesel in the upper layer was neutralized, washed with water and dehydrated to obtain 98.2 g of biodiesel (yield: 97.4%). The residue obtained after removing methanol and water from the lower ionic liquid phase is 1: 5.0 according to the molar ratio of glycerin and acetic acid, and toluene is used as the water-carrying agent. The by-product acetic acid is reclaimed under pressure, and the gained residue is allowed to stand for phase separation. The upper strata is glycerol triacetate, and the lower floor is an i...
Embodiment 3
[0021]Embodiment 3: 100g high acid value grease (acid value 12.5mgKOH / g), 42.2g methyl alcohol and 5.0g ionic liquid (3-sulfonic acid) propyltriethylammonium bromide ferrate (wherein 3-sulfonic acid chloride The molar ratio of acid propyltriethylammonium salt to ferric bromide is 1:2.5), added into the autoclave, heated and stirred, and reacted at 100°C for 10h. After static cooling, the mixture was taken out and allowed to stand for layering and phase separation. The upper layer of biodiesel was neutralized, washed with water and dehydrated to obtain 94.3 g of biodiesel (93.6% yield). The residue obtained after removing methanol and water from the lower ionic liquid phase is 1: 4.0 according to the molar ratio of glycerin and acetic acid, and toluene is used as the water-carrying agent. The by-product acetic acid is reclaimed under pressure, and the gained residue is allowed to stand for phase separation. The upper strata is glycerol triacetate, and the lower floor is an ioni...
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