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    • 3. 发明专利
    • PRODUCTION OF SESAME LIGNAN
    • JPH10120695A
    • 1998-05-12
    • JP31538796
    • 1996-10-22
    • BIZEN KASEI KKKADOYA SESAME MILLS
    • ISHIHARA TAKAFUMIOKADA KAZUYOSHI
    • C07G1/00C08H7/00
    • PROBLEM TO BE SOLVED: To efficiently produce a sesame lignan, having various physiological activities such as lowering actions on cholesterol and preventing actions on drunken sickness, useful as a healthy food, etc., and having high safety at a high concentration by carrying out the direct molecular distillation of a sesame oil. SOLUTION: Various sesame oils such as roasted oil, roasted and refined oil and raw pressed and refined oil are used as a raw material sesame oil and the direct molecular distillation thereof is carried out by using a falling film type molecular distilling machine at 150-270 deg.C temperature at 3wt.% sesamin content, various physiological activities such as lowering actions on cholesterol and preventing actions on drunken sickness, capable of greatly expecting usefulness as a healthy food, etc., and used by crystallization and tableting with a suitable excipient, carrier or additive or formation into a granule and formulating in confectioneries, bread, sprinklings, paste products or edible oils, dressings, mayonnaise, etc.
    • 6. 发明专利
    • EXTRACTING METHOD OF ANIMAL OR PLANT EXTRACT BY CELL MEMBRANE FREEZING DESTRUCTION
    • JPH0810503A
    • 1996-01-16
    • JP17982194
    • 1994-06-27
    • BIZEN KASEI KK
    • ISHIHARA TAKAFUMI
    • B01D11/02
    • PURPOSE:To efficiently produce a high purity extract by treating a tissue of an animal or a plant containing water at a specific temp. for a specific time sufficient for destructing the cell membrane, extracting an extract with a solvent, and next, removing the solvent from the extracted solution. CONSTITUTION:The tissue of animal or plant as it is or cutted into pieces of adequate size is treated at a sufficient temp for a necessary time for completely freezing the water in the tissue cell and destructing the cell wall. That is, the tissue, if necessary cutted into the pieces of 1-5mm size, is frozen at -15-(-25) deg.C until the raw materials are completely frozen. The time therefor is usually 48hr or above through it changes with the quality and quantity of the raw materials. Next, the frozen tissue is extracted with a hydrophilic solvent, preferably water or an alcoholic solvent, by a conventional method. For example, in the case of using a shucked oyster as the raw material, the shucked oyster is frozen at about -20 deg.C and is extracted with water as the extracting solvent at about 100 deg.C for 50-80min under stirring by heating with a jacket. Next, the extracted material is filtered, evacuated and condensed.