Patent classifications
C07C29/84
DEVICE FOR DISTILLATION DECOLORIZATION AND PURIFICATION OF ALCOHOL AND METHOD FOR PURIFICATION IN MALTOL PRODUCTION
Disclosed is a device for distillation decolorization and purification of alcohol in maltol production. The device comprises a rectification column, an alkali hydrolysis kettle and an alkali hydrolysis rectification column. An upper outlet of the rectification column is connected to an inlet of the alkali hydrolysis kettle, an outlet of the alkali hydrolysis kettle is connected to an inlet of the alkali hydrolysis rectification column, and an upper outlet of the alkali hydrolysis rectification column is connected to an inlet of a finished product tank. Further disclosed is a method for distillation decolorization and purification of alcohol in maltol production. A product processed by the solution of the present application has a high purity.
DEVICE FOR DISTILLATION DECOLORIZATION AND PURIFICATION OF ALCOHOL AND METHOD FOR PURIFICATION IN MALTOL PRODUCTION
Disclosed is a device for distillation decolorization and purification of alcohol in maltol production. The device comprises a rectification column, an alkali hydrolysis kettle and an alkali hydrolysis rectification column. An upper outlet of the rectification column is connected to an inlet of the alkali hydrolysis kettle, an outlet of the alkali hydrolysis kettle is connected to an inlet of the alkali hydrolysis rectification column, and an upper outlet of the alkali hydrolysis rectification column is connected to an inlet of a finished product tank. Further disclosed is a method for distillation decolorization and purification of alcohol in maltol production. A product processed by the solution of the present application has a high purity.
Systems and methods for rehabilitating alcohol
An assembly for rehabilitating alcohol, including a pressure controllable chamber, a cooler in thermal communication with the pressure controllable chamber, a liquid inlet port in fluidic communication with the pressure controllable chamber, a liquid outlet port in fluidic communication with the pressure controllable chamber, and a gas outlet port in fluidic communication with the pressure controllable chamber. The assembly further includes a partial vacuum source in fluidic communication with the gas outlet port for establishing a partial vacuum in the pressure controllable chamber, and a liquid collection vessel in fluidic communication with the liquid outlet port. The residence time from when a liquid is flowed into the pressure controllable chamber until the liquid exits the chamber is no more than sixty seconds. The partial vacuum is insufficient to evaporate an ethanol solution during residence time in the pressure controllable chamber.
Systems and methods for rehabilitating alcohol
An assembly for rehabilitating alcohol, including a pressure controllable chamber, a cooler in thermal communication with the pressure controllable chamber, a liquid inlet port in fluidic communication with the pressure controllable chamber, a liquid outlet port in fluidic communication with the pressure controllable chamber, and a gas outlet port in fluidic communication with the pressure controllable chamber. The assembly further includes a partial vacuum source in fluidic communication with the gas outlet port for establishing a partial vacuum in the pressure controllable chamber, and a liquid collection vessel in fluidic communication with the liquid outlet port. The residence time from when a liquid is flowed into the pressure controllable chamber until the liquid exits the chamber is no more than sixty seconds. The partial vacuum is insufficient to evaporate an ethanol solution during residence time in the pressure controllable chamber.
METHOD FOR MANUFACTURING 1,3-BUTYLENE GLYCOL, AND 1,3-BUTYLENE GLYCOL PRODUCT
Provided is a method capable of manufacturing 1,3-butylene glycol having a high potassium permanganate test value. A method for manufacturing 1,3-butylene glycol, which is a method for obtaining purified 1,3-butylene glycol from a crude reaction liquid containing 1,3-butylene glycol, the method including: a dehydration step of removing water by distillation; a high boiling substance removal step of removing a high boiling point component by distillation; and a product distillation step of obtaining purified 1,3-butylene glycol, wherein in the product distillation step, a product column is used in which a liquid feed having a 1,3-butylene glycol concentration of 97% or higher, an acetaldehyde content of 500 ppm or lower, and a crotonaldehyde content of 200 ppm or lower is distilled under a condition of a reflux ratio of higher than 0.1, and a liquid concentrated with acetaldehyde and crotonaldehyde is distilled off from above a feed plate, and 1,3-butylene glycol is extracted from below the feed plate.
1,3-BUTYLENE GLYCOL PRODUCT AND METHOD FOR PRODUCING 1,3-BUTYLENE GLYCOL
A high-purity 1,3-butylene glycol product is provided, which is colorless and odorless (or almost colorless and odorless), unlikely to cause coloration and odor over time, and, besides, unlikely to cause an acid concentration increase over time also in a state containing water. A 1,3-butylene glycol product in which at least one of a content of methyl vinyl ketone, a content of acetone, a content of butylaldehyde, a content of acetaldol, a content of a compound represented by Formula (1) below, a content of a compound represented by Formula (2) below, a content of a compound represented by Formula (3) below, and a total content of a compound represented by Formula (4) below and a compound represented by Formula (5) below, is less than 8 ppm.
METHOD FOR MANUFACTURING 1,3-BUTYLENE GLYCOL, AND 1,3-BUTYLENE GLYCOL PRODUCT
Provided is a method capable of manufacturing high-purity 1,3-butylene glycol having a high potassium permanganate test value, a very low content of low boiling point components, and a high initial boiling point with a high recovery rate.
The method for manufacturing 1,3-butylene is a method for obtaining purified 1,3-butylene glycol from a crude reaction liquid containing 1,3-butylene glycol. In a dehydration column used in a dehydration step, a liquid feed containing 1,3 butylene glycol and water with an acetaldehyde content of 1000 ppm or lower and a crotonaldehyde content of 400 ppm or lower is distilled under a condition of a reflux ratio of higher than 0.3, and a liquid concentrated with a low boiling point component containing water is distilled off from above a feed tray. In a product column used in a product distillation step, a liquid feed containing 1,3-butylene glycol with an acetaldehyde content of 500 ppm or lower and a crotonaldehyde content of 200 ppm or lower is distilled under a condition of a reflux ratio of higher than 0.1.
METHOD FOR MANUFACTURING 1,3-BUTYLENE GLYCOL, AND 1,3-BUTYLENE GLYCOL PRODUCT
Provided is a method capable of manufacturing high-purity 1,3-butylene glycol having a high potassium permanganate test value, a very low content of low boiling point components, and a high initial boiling point with a high recovery rate.
The method for manufacturing 1,3-butylene is a method for obtaining purified 1,3-butylene glycol from a crude reaction liquid containing 1,3-butylene glycol. In a dehydration column used in a dehydration step, a liquid feed containing 1,3 butylene glycol and water with an acetaldehyde content of 1000 ppm or lower and a crotonaldehyde content of 400 ppm or lower is distilled under a condition of a reflux ratio of higher than 0.3, and a liquid concentrated with a low boiling point component containing water is distilled off from above a feed tray. In a product column used in a product distillation step, a liquid feed containing 1,3-butylene glycol with an acetaldehyde content of 500 ppm or lower and a crotonaldehyde content of 200 ppm or lower is distilled under a condition of a reflux ratio of higher than 0.1.
1,2-ALKANEDIOLS AND A PROCESS FOR THEIR PRODUCTION
Suggested are 1,2-alkanediols of formula (I) HOCH.sub.2—CH(OH)—R.sup.1 in which R.sup.1 stands for an alkyl radical having 3 to 10 carbon atoms, said diols being substantially free of lactones and/or peroxides.
1,2-ALKANEDIOLS AND A PROCESS FOR THEIR PRODUCTION
Suggested are 1,2-alkanediols of formula (I) HOCH.sub.2—CH(OH)—R.sup.1 in which R.sup.1 stands for an alkyl radical having 3 to 10 carbon atoms, said diols being substantially free of lactones and/or peroxides.