Preparation method of high-flash demulsifier
A high-flash point demulsifier and high-pressure reactor technology, applied in the direction of dehydration/demulsification by chemical methods, can solve problems such as poor hydrophilicity, production, storage, transportation and on-site safety risks of demulsifiers, and achieve good low-temperature demulsification. The effects of milk properties, good hydrophilic and lipophilic properties, and strong surface activity
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[0019] (1) Preparation of intermediates: add 0.2-0.5 parts by weight of catalyst potassium hydroxide and 1-2 parts by weight of glycerin as an initiator in a stainless steel autoclave, vacuumize and fill with nitrogen at 20-30°C Replace the air in the kettle three times each time, raise the temperature to 110-130°C, feed 97.5-110.5 parts by weight of propylene oxide, and control the reaction pressure to 0.3-0.5 MPa, and then reduce the pressure after 2-2.5 hours until the pressure does not change anymore , to obtain an intermediate;
[0020] (2) Preparation of ethylene oxide and propylene oxide block copolyether: add 0.2 to 0.3 parts by weight of catalyst potassium hydroxide and 15 to 20 parts by weight of potassium hydroxide prepared in step (1) into a stainless steel autoclave The intermediate was evacuated and filled with nitrogen three times respectively, dehydrated in vacuum at -0.15Mpa pressure and 100°C for 2 to 3 hours, introduced 79.7 parts by weight of ethylene oxide...
Embodiment 1
[0026] The present invention is realized through the following steps:
[0027] (1) Preparation of intermediates: Add 0.2 parts by weight of catalyst potassium hydroxide and 1 part by weight of initiator glycerin into a stainless steel autoclave, vacuumize and fill with nitrogen three times at 20°C to replace the inside of the autoclave The air was heated up to 110°C, 97.5 parts by weight of propylene oxide was introduced, and the reaction pressure was controlled to be 0.3MPa, and after 2 hours, the pressure was reduced until the pressure no longer changed, and the intermediate was obtained;
[0028] (2), preparation of ethylene oxide and propylene oxide block copolyether: add 0.23 parts by weight of catalyst potassium hydroxide and 15 parts by weight of the intermediate prepared by step (1) into the stainless steel autoclave, pump Vacuum and nitrogen filling three times respectively, vacuum dehydration at -0.15Mpa pressure, 100°C temperature for 2 hours, feed 79.7 parts by wei...
Embodiment 2
[0033] The present invention is realized through the following steps:
[0034] (1) Preparation of intermediates: Add 0.35 parts by weight of catalyst potassium hydroxide and 1.5 parts by weight of initiator glycerin into a stainless steel autoclave, vacuumize and fill with nitrogen three times at 25°C to replace the inside of the autoclave The air was heated up to 120°C, 104 parts by weight of propylene oxide was introduced, and the reaction pressure was controlled to be 0.4MPa. After 2.25 hours, the pressure was reduced until the pressure did not change, and the intermediate was obtained;
[0035] (2), preparation of ethylene oxide and propylene oxide block copolyether: add 0.25 parts by weight of catalyst potassium hydroxide and 17.5 parts by weight of the intermediate prepared by step (1) into the stainless steel autoclave, pump Vacuum and nitrogen filling three times respectively, vacuum dehydration at -0.15Mpa pressure, 100°C temperature for 2.5 hours, feed 79.7 parts by ...
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