Process for preparation of methacrylic acid and methacrylic acid esters

一种甲基丙烯酸酯、甲基丙烯酸的技术,应用在甲基丙烯酸的制备领域,能够解决没有教导回收甲基丙烯酸等问题

Inactive Publication Date: 2014-05-28
EVONIK ROEHM GMBH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The disadvantage of membrane filtration is that, in general, large volumes of water (often using the wastewater itself) are required to flush out components that do not pass through the filter
However, recovery of methacrylic acid from waste oil is not taught in any of these documents

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0201] Example 1 describes how Figure 4 part of the method shown. 82.1% by weight of MAA, 14.3% by weight of various and partially unknown high boilers (dimeric and oligomeric MAA, maleic acid, terephthalic acid, citraconic acid, polymer etc.) and 3.6% by weight of inhibitors (mainly hydroquinone) and the first aqueous phase containing 0.6% by weight of MAA and 5.0% by weight of high-boiler compounds isolated from the first extraction unit A3 at a ratio of 1:80 The ratio of the high boiler phase to the first aqueous phase is combined in the merging unit R. The concentrations in the resulting combined phase were measured to be 1.6% by weight of MAA and 5.1% by weight of high boilers. The combined phases are extracted in a second separation unit B with n-hexane. 4.9% by weight of MAA was produced in the organic phase, compared to 3.9% by weight of MAA in the comparative case when the first aqueous phase was not combined with the high boiler phase.

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PUM

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Abstract

The invention relates to a process for preparation of at least one of methacrylic acid and a methacrylic acid ester, comprising process steps: a1) gas phase oxidation of at least one C4 compound to obtain a reaction phase comprising methacrylic acid; a2) quenching of the reaction phase to obtain a crude aqueous phase comprising methacrylic acid; a3) extraction of at least a part of the methacrylic acid from the crude aqueous phase comprising methacrylic acid into an organic solvent to obtain a crude organic phase comprising methacrylic acid and a first aqueous phase, wherein the first aqueous phase comprises components: i. at least 65 wt.%, preferably in the range of from 65 wt.% to 99.9 wt.%, more preferably in the range of from 70 wt.% to 99.8 wt.% water, yet more preferably in the range of from 75 wt.% to 99 wt.%, more preferably in the range of from 76 wt.% to 98.5 wt.%, more preferably in the range of from 77 wt.% to 98 wt.%, even more preferably in the range of from 78 wt.% to 97.5 wt.%, even more preferably in the range of from 79 wt.% to 95 wt.%, yet more preferably in the range of from 80 wt.% to 90 wt.% water, based on the total weight of the first aqueous phase, and ii. not more than 35 wt.%, preferably in the range of from 0.1 wt.% to 35 wt.%, preferably in the range of from 0.2 wt.% to 30 wt.%, more preferably in the range of from 1 wt.% to 25 wt.%, yet more preferably in the range of from 1.5 wt.% to 24 wt.%, more preferably in the range of from 2 wt.% to 23 wt.%, even more preferably in the range of from 2.5 wt.% to 22 wt.%, even more preferably in the range of from 5 wt.% to 21 wt.%, yet more preferably in the range of from 10 wt.% to 20 wt.% of at least one organic compound, based on the total weight of the first aqueous phase, wherein the sum of the weight amounts of i. and ii. is 100 wt.%; a4) separation and optionally purification of at least a part of the methacrylic acid from the crude organic phase comprising methacrylic acid; a5) optionally, esterification of at least a part of the methacrylic acid obtained in step a4); b) separation of at least a part of the water comprised in the first aqueous phase obtained in step a3) from at least a part of at least one component ii. to obtain a second aqueous phase and an organic phase, wherein the organic phase comprises at least one component ii., and wherein the second aqueous phase is depleted in at least one component ii. compared to the first aqueous phase; c) optionally, separation of at least a part of at least one organic compound from the second aqueous phase obtained in process step b) to obtain a third aqueous phase; d) optionally, separation of at least a part of at least one component ii from the organic phase obtained in process step b), to a process for treatment of an aqueous phase comprising at least one organic compound, and a device for production of at least one of methacrylic acid and a methacrylic ester.

Description

technical field [0001] The invention relates to a process for the production of methacrylic acid, a process for the production of methacrylate esters and a process for the treatment of an aqueous phase comprising at least one organic compound. Background technique [0002] Methacrylic acid (MAA) and methacrylates, such as methyl methacrylate (MMA) and butyl methacrylate, are used in a wide variety of applications. The industrial production of methacrylic acid takes place in particular by heterogeneously catalyzed gas-phase oxidation of isobutene, tert-butanol, methacrolein or isobutyraldehyde. The gaseous reaction phase thus obtained is converted into an aqueous solution of methacrylic acid by cooling and condensation, optionally separated from low-boiling substances such as acetaldehyde, acetone, acetic acid, acrolein and methacrolein, and then introduced into a solvent extraction column , to extract and separate methacrylic acid using a suitable extractant, such as a shor...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07C51/42C07C51/43C07C51/44C07C51/48C07C67/08C07C69/54C07C57/04C07C57/07B01D9/00B01D11/00
CPCB01D9/0013B01D9/0036B01D9/0045C07C1/20C07C29/10C07C51/252C07C51/42C07C51/48C07C67/08C07C67/58C07C57/04C07C69/54C07C31/04C07C11/09C07C51/43C07C51/44
Inventor H·舍费尔T·巴尔多夫
Owner EVONIK ROEHM GMBH
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