Edible wild fungus oil
A wild fungus and wild fungus technology, applied in the field of edible oil, can solve the problems of destroying the special flavor of wild fungus, small wild fungus origin, loss of nutrients, etc. Effect
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Embodiment 1
[0014] Example 1: Select and dry 100kg matsutake, crush it into 70-mesh bacterial powder, put the bacterial powder into the extraction kettle for extraction, heat and pressurize the extraction kettle, control the temperature at 40-45°C, and the pressure at 35 Mpa. After stabilization, the supercritical carbon dioxide is introduced, the supercritical carbon dioxide penetrates into the wild bacterial cells, the oil and fat-soluble components in the cells seep out, dissolve into the supercritical carbon dioxide, and enter the No. 1 separation kettle with low temperature and pressure for a separation. The temperature is controlled at 35-40°C and the pressure is 5 Mpa. The oil and fat-soluble components dissolved in supercritical carbon dioxide are separated, and the supercritical carbon dioxide with a part of oil and fat-soluble components enters the No. 2 separation tank with a lower temperature, and the remaining The fat and fat-soluble components are separated, and the car...
Embodiment 2
[0016] Embodiment 2, select and dry boletus 100kg, pulverize into 75 purpose bacterium powder, bacterium powder is put into extraction kettle, heat and pressurize in the extraction kettle, temperature is controlled at 40-45 ℃, pressure 35 Mpa, After the pressure is stabilized, introduce supercritical carbon dioxide, supercritical carbon dioxide penetrates into the wild bacterial cells, the oil and fat-soluble components in the cells seep out, dissolve into supercritical carbon dioxide, and enter the No. 1 separation kettle with low temperature and pressure for one time Separation, the temperature is controlled at 35-40 ° C, the pressure is 5 Mpa, the oil and fat-soluble components dissolved in supercritical carbon dioxide are separated, and the supercritical carbon dioxide with a part of oil and fat-soluble components enters the No. 2 separation kettle with a lower temperature , the remaining oil and fat-soluble components are separated, and the carbon dioxide returns to the su...
Embodiment 3
[0019] Example 3. Select and dry 100kg of Ganoderma lucidum, crush it into 80-mesh bacterial powder, put the bacterial powder into the extraction kettle, heat and pressurize the extraction kettle, the temperature is controlled at 40-45°C, and the pressure is 35 Mpa. After stabilization, the supercritical carbon dioxide is introduced, the supercritical carbon dioxide penetrates into the wild bacterial cells, the oil and fat-soluble components in the cells seep out, dissolve into the supercritical carbon dioxide, and enter the No. 1 separation kettle with low temperature and pressure for a separation. The temperature is controlled at 35-40°C and the pressure is 5 Mpa. The oil and fat-soluble components dissolved in supercritical carbon dioxide are separated, and the supercritical carbon dioxide with a part of oil and fat-soluble components enters the No. 2 separation tank with a lower temperature, and the remaining The fat and fat-soluble components are separated, and the carbon ...
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