Method for refining biologic diesel oil, phospholipid and glycerin by using leftovers of vegetable oil
A technology of biodiesel and scraps, which is applied in the directions of edible phospholipid compositions, biofuels, biological raw materials, etc., can solve the problems of waste of natural resources, environmental pollution, insufficient utilization of scrap resources, etc., and achieves improved conversion rate, emission No pollution, fast response time
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Embodiment 1
[0022] Fully mix 400g of fresh soybean oil scraps (oil bottoms, soap stock mixture) with 40ml saturated salt water, and stir for 10 minutes. Add 800ml of n-hexane and mix thoroughly and then stir for 20 minutes. After centrifugation, it is divided into 3 layers: the upper layer is the organic phase, the middle layer is soap, and the lower layer is the water phase. Take the upper organic phase and rotate it to evaporate, recover the organic solvent, dissolve the concentrate with ether, and then add an appropriate amount of acetone of the same volume, immediately a light yellow precipitate precipitates out. Suction filtration under reduced pressure to collect the filter cake. The filter cake was vacuum-dried at 50°C to obtain 12.8 g of light yellow phospholipid. The filtrate was then rotary evaporated to recover acetone, and the remaining part was neutral oil. Take 100g of the neutral oil obtained by combining multiple extractions and dehydrate it and add it to a 500ml three-n...
Embodiment 2
[0024] Fully mix 400g of fresh rapeseed oil scraps (oil bottoms, soap stock mixture) with 20ml saturated salt water, and stir for 20 minutes. Add 400ml of petroleum ether and mix thoroughly, then stir for 30 minutes. After centrifugation, it is divided into 3 layers: the upper layer is the organic phase, the middle layer is soap, and the lower layer is the water phase. The upper organic phase was rotary evaporated, the organic solvent was recovered, the concentrate was dissolved in ether, and then twice the volume of cold acetone (4°C) was added, and a pale yellow precipitate immediately precipitated out. Suction filtration under reduced pressure to collect the filter cake. The filter cake was vacuum-dried at 40°C to obtain 8.62 g of light yellow phospholipid. The filtrate was then rotary evaporated to recover acetone, and the remaining part was neutral oil. Take 100g of the neutral oil obtained by combining multiple extractions, dehydrate it, and add it to a 500ml three-nec...
Embodiment 3
[0026] Fully mix 400g of fresh cottonseed scraps (oil foot, soap foot mixture) with 60ml saturated salt water, and stir for 10 minutes. Add 400ml of diethyl ether and mix thoroughly and then stir for 30 minutes. After centrifugation, it is divided into 3 layers: the upper layer is the organic phase, the middle layer is the soap, and the lower layer is the aqueous phase. The upper organic phase was rotary evaporated, the organic solvent was recovered, the concentrate was dissolved in ether, and then three times the volume of acetone was added, and a light yellow precipitate was immediately precipitated. Suction filtration under reduced pressure to collect the filter cake. The filter cake was vacuum-dried at 60°C to obtain 11.46 g of light yellow phospholipid. The filtrate was then rotary evaporated to recover acetone, and the remaining part was neutral oil. Take 100g of the neutral oil obtained by combining multiple extractions, dehydrate it, and add it to a 500ml three-neck ...
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