Process for continuously recovering (meth)acrylic acid and apparatus for the process

US9962625B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9962625-B2
Application numberUS-201414903206-A
CountryUS
Kind codeB2
Filing dateJul 21, 2014
Priority dateJul 22, 2013
Publication dateMay 8, 2018
Grant dateMay 8, 2018

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Abstract

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This disclosure relates to a method for continuous recovery of (meth)acrylic acid and an apparatus used for the recovery method. The method of continuous recovery of (meth)acrylic acid according to the present invention may remarkably reduce the amount of extraction solvent used and energy consumption of the total process, and minimize polymerization of (meth)acrylic acid in the recovery process, thus enabling stable recovery of (meth)acrylic acid and operation of a continuous process.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method for continuous recovery of (meth)acrylic acid, comprising: an absorption process wherein a mixed gas including (meth)acrylic acid, organic by-products, and vapor, which is produced by a synthesis reaction of (meth)acrylic acid, is contacted with water to obtain a (meth)acrylic acid aqueous solution; an extraction process wherein the (meth)acrylic acid aqueous solution obtained through the absorption process is contacted with an extraction solvent in an extraction column to obtain a (meth)acrylic acid extract solution and a raffinate solution; and a distillation process wherein a feed including the (meth)acrylic acid extract solution obtained through the extraction process is distilled to obtain (meth)acrylic acid, wherein the absorption process is conducted in a packed column type of (meth)acrylic acid absorption tower, a weight ratio of the extraction solvent to the (meth)acrylic acid aqueous solution fed to the extraction column is greater than 0.3 and less than 1.0, and the raffinate solution obtained through the extraction process is fed to at least one point corresponding to 10 to 30% below the uppermost part based on the total height of the column packing within the (meth)acrylic acid absorption tower. 2. A method for continuous recovery of (meth)acrylic acid, comprising: an absorption process wherein a mixed gas including (meth)acrylic acid, organic by-products, and vapor, which is produced by a synthesis reaction of (meth)acrylic acid, is contacted with water to obtain a (meth)acrylic acid aqueous solution; an extraction process wherein the (meth)acrylic acid aqueous solution obtained through the absorption process is contacted with an extraction solvent in an extraction column to obtain a (meth)acrylic acid extract solution and a raffinate solution; and a distillation process wherein a feed including the (meth)acrylic acid extract solution obtained through the extraction process is distilled to obtain (meth)acrylic acid, wherein the absorption process is conducted in a multistage tray type of (meth)acrylic acid absorption tower, a weight ratio of the extraction solvent to the (meth)acrylic acid aqueous solution fed to the extraction column is greater than 0.3 and less than 1.0, and the raffinate solution obtained through the extraction process is fed to at least one point corresponding to 10 to 30% below the uppermost stage of the multistage trays present within the (meth)acrylic acid absorption tower based on the total number of stages within the multistage tray type of (meth)acrylic acid absorption tower. 3. The method for continuous recovery of (meth)acrylic acid according to claim 1 , wherein the extraction solvent is a hydrophobic solvent having a boiling point of 10 to 120° C. 4. The method for continuous recovery of (meth)acrylic acid according to claim 1 , wherein the extraction solvent is at least one selected from the group consisting of benzene, toluene, xylene, n-heptane, cycloheptane, cycloheptene, 1-heptene, ethyl-benzene, methyl-cyclohexane, n-butyl acetate, isobutyl acetate, isobutyl acrylate, n-propyl acetate, isopropyl acetate, methyl isobutyl ketone, 2-methyl-1-heptene, 6-methyl-1-heptene, 4-methyl-1-heptene, 2-ethyl-1-hexene, ethylcyclopentane, 2-methyl-1-hexene, 2,3-dimethylpentane, 5-methyl-1-hexene, and isopropyl-butyl-ether. 5. The method for continuous recovery of (meth)acrylic acid according to claim 1 , wherein the extract solution obtained through the extraction process includes 30 to 60 wt % of (meth)acrylic acid, 30 to 60 wt % of an extraction solvent, 3 to 10 wt % of water, and a remaining amount of organic by-products. 6. The method for continuous recovery of (meth)acrylic acid according to claim 1 , wherein the raffinate solution obtained through the extraction process includes (meth)acrylic acid in a content of 15 wt % or less. 7. The method for continuous recovery of (meth)acrylic acid according to claim 1 , wherein the synthesis reaction of (meth)acrylic acid is an oxidation reaction of at least one compound selected from the group consisting of propane, propylene, butane, isobutylene, and (meth)acrolein in the presence of a gas phase catalyst.

Assignees

Inventors

Classifications

  • B01D3/143Primary

    by two or more of a fractionation, separation or rectification step · CPC title

  • Acrylic acid; Methacrylic acid · CPC title

  • by liquid-liquid treatment · CPC title

  • by change of the physical state, e.g. crystallisation · CPC title

  • C07C51/44Primary

    by distillation · CPC title

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What does patent US9962625B2 cover?
This disclosure relates to a method for continuous recovery of (meth)acrylic acid and an apparatus used for the recovery method. The method of continuous recovery of (meth)acrylic acid according to the present invention may remarkably reduce the amount of extraction solvent used and energy consumption of the total process, and minimize polymerization of (meth)acrylic acid in the recovery proces…
Who is the assignee on this patent?
Lg Chemical Ltd
What technology area does this patent fall under?
Primary CPC classification B01D3/143. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue May 08 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).