CN1225446C - Process for preparing aromatic carboxylic acid - Google Patents
Process for preparing aromatic carboxylic acid Download PDFInfo
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- CN1225446C CN1225446C CNB01116476XA CN01116476A CN1225446C CN 1225446 C CN1225446 C CN 1225446C CN B01116476X A CNB01116476X A CN B01116476XA CN 01116476 A CN01116476 A CN 01116476A CN 1225446 C CN1225446 C CN 1225446C
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C63/00—Compounds having carboxyl groups bound to a carbon atoms of six-membered aromatic rings
- C07C63/14—Monocyclic dicarboxylic acids
- C07C63/15—Monocyclic dicarboxylic acids all carboxyl groups bound to carbon atoms of the six-membered aromatic ring
- C07C63/26—1,4 - Benzenedicarboxylic acid
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/23—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/25—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring
- C07C51/252—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring of propene, butenes, acrolein or methacrolein
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/255—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of compounds containing six-membered aromatic rings without ring-splitting
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/255—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of compounds containing six-membered aromatic rings without ring-splitting
- C07C51/265—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of compounds containing six-membered aromatic rings without ring-splitting having alkyl side chains which are oxidised to carboxyl groups
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/43—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
- C07C51/44—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation by distillation
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/47—Separation; Purification; Stabilisation; Use of additives by solid-liquid treatment; by chemisorption
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/48—Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
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Abstract
A process for producing an aromatic carboxylic acid under high pressure and high temperature by subjecting an alkylaromatic compound to a liquid phase oxidation by a molecular oxygen-containing gas in the presence of an oxidation catalyst in a reaction solvent comprising an aliphatic carboxylic acid in an oxidizing reactor while recovering the aliphatic carboxylic acid by distillation of the oxidation exhaust gas, in which the recovery of the aliphatic carboxylic acid can be attained efficiently under separation thereof from by-products, such as water and alcohols, with permission of easier waste water treatment, wherein the process comprises proceeding the reaction while removing the water and the alcohol formed by the oxidation reaction by means of membrane-separation.
Description
The present invention relates to the method that a kind of liquid-phase oxidation by alkylaryl compounds prepares aromatic carboxylic acid, this alkylaryl compounds contain one or more substituted alkyls or the part by the groups of molecular oxygen-containing gas oxidation.
Aromatic carboxylic acid is important Essential Chemistry product, especially is used as the starting material of fiber, resin and similar substance.It for example, has been found that in recent years the demand of terephthalic acid increases day by day, because of can be used as the raw material of producing trevira.In order to prepare aromatic carboxylic acid, the general so far method of using is the aromatics experience liquid-phase oxidation that will be replaced by alkyl, this aromatics and molecular oxygen-containing gas are contacted in reaction solvent, this solvent comprises a kind of low aliphatic carboxylic acid, as acetate, reaction is to carry out under the condition that oxide catalyst exists in an oxidation reactor, and said catalyzer is made up of heavy metal compound and bromine-containing compound.In this preparation method, by being conducted in the oxidation reactor as the alky-substituted aromatic compound (as p-Xylol) of raw material, the mixture of forming as the acetate and the catalyzer of reaction solvent, import molecular oxygen-containing gas (as air) simultaneously and impel oxidation, thereby prepare a kind of aromatic carboxylic acid (as terephthalic acid).
In a kind of method that has the people to propose, be condensed at condensing steps from the oxidation reactor expellant gas, the condensation product of formation is imported into distillation tower and distills, and the fraction that contains reaction solvent that obtains is imported oxidation reactor again.A kind of method was also proposed, wherein distillation tower is set to the top connection of reactor, the discharge gas of oxidation is distillated under the heat energy of himself with the recovery reaction solvent, and with (the Japan clear 54-14098B of special permission communique speciallys permit with Japan and discloses flat 6-279353A) in the reaction solvent circulation importing oxidation reactor.In this method, the water of condensation cooling that the cat head distillate gas of discharging from the distillation tower top is condensed the device is discharged the steam that contains in the gas with condensation, and resulting condensation product is back to distillation tower.
In this technology, comprise the discharge gas of oxidation or the distillation of its condensation product, the height of distillation tower should be enough high to reclaim reaction solvent (as acetate), reaction solvent is separated fully, because lower distillation tower height can make a part of reaction solvent move to condensation side in distillation tower with water and alcohol.Because water is to form in oxidizing reaction, a part of condensation product should be discharged from reactive system, can produce unfavorable factor owing to being entrained with reaction solvent etc. in wastewater treatment.
A kind of method has also been proposed in addition, the alphatic carboxylic acid ester that wherein forms in oxidizing reaction (as methyl acetate etc.) is collected by the absorption of washing water, and spent ion exchange resin makes this carboxyester hydrolysis to reclaim corresponding aliphatic carboxylic acid and again as reaction solvent as hydrolyst.Yet it is very difficult separating pure and mild aliphatic carboxylic acid.
The purpose of this invention is to provide a kind of method that is used to prepare the aromatic carboxylic acid, wherein aliphatic carboxylic acid can be separated effectively from byproduct (as water and alcohol) and obtain to reclaim effectively, makes wastewater treatment become easy simultaneously.
Another object of the present invention provides a kind of method that is used to prepare aromatic carboxylic acid, wherein the alphatic carboxylic acid ester that forms in reactive system is carried out hydrolysis effectively to reclaim useful composition.
It is as follows that the present invention prepares the method for aromatic carboxylic acid:
(1) a kind of method for preparing aromatic carboxylic acid, in the oxidation reactor under the High Temperature High Pressure, make alkyl aromatic compound in reaction solvent, carry out liquid phase oxidation reaction with molecular oxygen-containing gas, there is oxide catalyst in the reaction, said reaction solvent comprises a kind of aliphatic carboxylic acid, and described method comprises:
When reaction is carried out by divided thin film from removing water and the alcohol that in oxidizing reaction, forms.
(2) as said method in above-mentioned (1), wherein this method comprises the steps:
Make alkyl aromatic compound carry out liquid phase oxidation reaction with molecular oxygen-containing gas in the oxidation reactor under the High Temperature High Pressure in reaction solvent, have oxide catalyst in the reaction, said reaction solvent comprises a kind of aliphatic carboxylic acid,
The oxidizing reaction waste gas that to discharge from oxidation reactor imports distillation tower, perhaps oxidizing reaction waste gas is imported the oxidizing reaction off-gas condenser and the gained condensation product is imported distillation tower, in distillation tower, oxidizing reaction waste gas or condensation product are distilled, the distillation fraction that will contain reaction solvent simultaneously is back in the oxidation reactor, gas by cooling distillation cat head in condenser condenses to form condensation product it, to condensation product carry out divided thin film from, water and alcohol arrive permeate side by film permeation, and aliphatic carboxylic acid is still stayed the enriched material side and obtain recovery.
(3) as above-mentioned (2) said method, wherein this method also comprises an absorption step, and this step comprises the discharge gas of condensing steps and absorption liquid are contacted absorbing alphatic carboxylic acid ester, and the absorption liquid that will so obtain offers membrane separation step.
(4) as above-mentioned (2) said method, wherein this method also comprises an absorption step, this step comprises oxidizing reaction off-gas condenser expellant gas and a kind of absorption liquid is contacted absorbing alphatic carboxylic acid ester, and the absorption liquid that will so obtain offers membrane separation step.
(5) any one said method in above-mentioned (2) to (4), wherein this method also comprises a hydrolysing step, comprise condensation product and/or absorption liquid and/or divided thin film are contacted with hydrolyst decomposing alphatic carboxylic acid ester from penetrant and/or enriched material, and the hydrolysate that obtains is conducted to membrane separation step.
(6) any one said method in above-mentioned (1) to (5), wherein divided thin film is from being to use a kind of reverse osmosis membrane to carry out.
(7) any one said method in above-mentioned (4) to (6), wherein hydrolyst is a kind of ion exchange resin.
(8) above-mentioned (1) any one said method in (7), wherein condensation product all or part of through divided thin film from and enriched material is back to distilation steps.
(9) any one said method in above-mentioned (1) to (8), wherein divided thin film is from carrying out in a plurality of separation phases.
Fig. 1 is the schema of the embodiment of the present invention's method of preparing terephthalic acid.
Fig. 2 is the schema of another embodiment of the present invention's method of preparing terephthalic acid.
Fig. 3 is the schema of another embodiment of the present invention's method of preparing terephthalic acid.
Fig. 4 is the schema of another embodiment of the present invention's method of preparing terephthalic acid.
Fig. 5 is the schema of another embodiment of the present invention's method of preparing terephthalic acid.
Implement preferred embodiments of the present invention
According to the present invention, the water and the alcohol of leaving away and generating by divided thin film when oxidizing reaction is carried out except that in the reaction.For aliphatic carboxylic acid (as acetate) is separated effectively with as reaction solvent from by product (as the water and the alcohol of reaction generation), preferably distilation steps and membrane separation step are combined here.Only realize that if separate the ratio that just height of distillation tower need be designed is higher as previously mentioned by distilling.On the other hand, if only separate by divided thin film from realizing that separation efficiency is lower like this, thereby the multistage divided thin film of needs from.Yet, realize the separation of the overwhelming majority by using highly lower distillation tower, and separate from product of distillation low concentration by divided thin film, just can realize high efficiency separation by bantam like this.
The starting material that prepare aromatic carboxylic acid as the method according to this invention by oxidation, can use aromatics as described below, this aromatics has one or more substituted alkyls or partial oxidation alkyl group (hereinafter being sometimes referred to as oxidable raw material).A kind of like this aromatics is also polynuclear compound of monocyclic compound both.As the substituted alkyl group, can be that carbonatoms is the alkyl of 1-4, as methyl, ethyl, n-propyl group and sec.-propyl.As the alkyl group of partial oxidation, can be aldehyde radical, acyl group, carboxyl and hydroxyalkyl.
The specific examples of alky-substituted aromatic hydrocarbon comprises have 2-4 the alkyl dialkyl benzene or the polyalkylbenzene of (carbonatoms is 1-4), as m-Diisopropylbenzene, p-Diisopropylbenzene, a cymene, p-cymene, m-xylene, p-Xylol, Three methyl Benzene and tetramethyl-benzene; Dialkyl group naphthalene or many alkylnaphthalenes with 2-4 alkyl (carbonatoms is 1-4) are as dimethylnaphthalene, diethyl naphthalene and isopropyl naphthalene; And the many alkyl biphenyls with 2-4 alkyl (carbonatoms is 1-4), as dimethyl diphenyl.
Aromatics with substituted alkyl of one or more partial oxidation is that wherein one or more as mentioned above substituted alkyls are the compound of aldehyde radical, acyl group, carboxyl and hydroxyalkyl by partial oxidation.Its concrete example comprises 3-tolyl aldehyde, 4-tolyl aldehyde, a toluic acid, to toluic acid, 3-carbamoyl benzoate, 4-carbamoyl benzoate and 2-methyl-6-formyl-naphthalene.They both can use separately, also can two or more unite use.
The method according to this invention, a kind of heavy metal compound and a kind of bromine compounds are used as catalyzer.These examples for compounds are as shown below: as the heavy metal in the heavy metal compound for example cobalt, manganese, nickel, chromium, zirconium, copper, lead, hafnium and cerium.They both can use separately, also can two or more be used in combination, the combination of wherein preferred cobalt and manganese.
For such heavy metal compound, can be acetate, nitrate, acetylacetonate compound, naphthenate, stearate and bromide, wherein preferred acetate.
For bromine compounds, both can be molecular bromine; Also inorganic bromine compounds is as hydrogen bromide, Sodium Bromide, Potassium Bromide, cobaltous bromide and Manganese dibromide; Organbromine compound also is as methyl bromide, methylene bromide, methenyl bromide, bromobenzene, bromo toluene, ethylene dibromide, tribromoethane and tetrabromoethane.They both can use separately, also can two or more be used in combination.
The ratio of bromine atoms and heavy metal atom is in the catalyzer of being made up of heavy metal compound and bromine compounds according to the present invention: with respect to every mole of heavy metal bromine atoms is the 0.05-10 mole, is preferably the 0.1-2 mole.The common consumption of this catalyzer is counted 10-10 with the concentration of heavy metal, and 000ppm (weight) is preferably 100-5,000ppm (weight).
In the method according to the invention, in order to prepare aromatic carboxylic acid, make oxidable raw material (aromatics) in oxidation step, liquid-phase oxidation take place in reaction solvent with molecular oxygen-containing gas, said reaction solvent comprises a kind of lower alphatic carboxylic acid, and reaction is to carry out under the condition that said in the above oxide catalyst exists in an oxidation reactor.
As for molecular oxygen-containing gas, for example can be oxygen and air, because air is easy to obtain thereby uses usually air.The amount of the oxygen-containing gas that is added in the reaction is above aromatics (as oxidable raw material) is oxidized to the required amount of aromatic carboxylic acid.When air was used as molecular oxygen-containing gas, the flow of the air that infeeds in reactive system was 2-20Nm with respect to 1 kilogram of aromatics (as oxidable raw material)
3, be preferably 2.5-15Nm
3
The specific examples that is used as the lower alphatic carboxylic acid of reaction solvent can be acetate, propionic acid and butyric acid.Lower alphatic carboxylic acid both can be used alone as reaction solvent, also can mix as reaction solvent with water.The specific examples of reaction solvent comprises acetate, propionic acid, butyric acid and composition thereof, and the mixture of they and water.In above-mentioned example, the mixture of preferred acetate and water, especially the amount of water is the 1-20 weight part with respect to the acetate of 100 weight parts, is preferably the 5-15 weight part.
The temperature that oxidizing reaction is carried out generally between 100-250 ℃, is preferably 150-220 ℃.The pressure of oxidizing reaction remains on any pressure on the pressure of liquid phase for making reactive system.
By carrying out oxidizing reaction in the above described manner, can obtain and the corresponding aromatic carboxylic acid of aromatics (as oxidable raw material).As the specific examples of aromatic carboxylic acid, can be aromatic dicarboxilic acid, as terephthalic acid, m-phthalic acid, 2,6-naphthalene dicarboxylic acids and 4,4 '-diphenyl dicarboxylic acid; The fragrant tricarboxylic acid, as trimellitic acid and 1,3, the 5-benzenetricarboxylic acid; And aromatic polycarboxylic acids, as 1,2,4,5-pyromellitic acid etc.
The method of aromatic carboxylic acid produced according to the present invention can be used for preparing aromatic dicarboxilic acid, perhaps is used for preparing insoluble or is insoluble in the aromatic carboxylic acid of reaction solvent, in particular for the preparation terephthalic acid.
The aromatic carboxylic acid of Xing Chenging (as terephthalic acid) can come out to form slurries with crystal settling like this, slurries is discharged and pass through solid/liquid separation with the recovery crystal from oxidation reactor, thereby obtain raw product, as thick terephthalic acid.
In the crystal of resulting raw product, also contain impurity, impurity comprises the intermediate product of oxidizing reaction, so raw product also will pass through purifying step, comprise the dissolving raw product, carry out oxide treatment, reduction is handled and is made target product (being terephthalic acid) crystallization, thereby must be to the crystalline slurries that contain product.By collect crystal from slurries, the target product after just can being purified is as the purified terephthalic acid.
In distilation steps, advantageously the discharge gas with oxidation imports the distillation tower (high pressure distillation tower) that links to each other with the oxidation reactor top, the heat that utilizes oxidizing reaction to discharge is realized distillation procedure, the condensation product that forms in the oxidizing reaction off-gas condenser simultaneously also can carry out distillation procedure in distillation tower, wherein the discharge gas of oxidation imports distillation tower (atmospheric distillation tower) through condensation with condensation product.In both cases, the fraction that contains reaction solvent is collected in the bottom of distillation tower and is back to oxidation reactor, and distillation tower top distilled contains the top discharge of the gas of water vapour and noncondensable gas from distillation tower.Distillation tower can be the distillation tower that is independent of oxidation reactor, as disclosed among the clear 54-14098B of Japan special permission communique, or the distillation tower that directly links to each other with the oxidation reactor top, as Japan specially permit disclose among the flat 6-279353A disclosed.Distillation tower can be a plate tower, is preferably packing tower, and described packing tower preferably has the device of collection fine solid particles (as the aromatic carboxylic acid crystal), for example is arranged on one or more solid matter catch traies of the bottom of packing tower.
Distillation tower is preferably built by this way: a plurality of attached towers are connected in turn, make from attached tower section the preceding expellant gas after the attached tower section that links to each other in turn in proceed distillation, to be back to attached the preceding tower section at the overhead product in the attached tower section in back, wherein being in an emergency during shut-down operation, the optimum seeking site that overhead product is discharged from system is the middle part between attached tower, in case the reduction of the concentration of the reaction liquid in the oxidation reactor and temperature.
By using such distillation tower to make the discharge gas distillation of oxidation, or the condensation product of discharging from the oxidizing reaction off-gas condenser is distilled, wherein the discharge gas of oxidation is through concentrating, and the fraction of carrying secretly in the discharge gas of oxidation that contains reaction solvent is recycled to oxidation reactor.Except reaction solvent, these fractions also comprise unreacted alkyl-aromatic compounds, the aromatic carboxylic acid that is generated and catalyzer etc., and all there is and is collected in the bottom of distillation tower in they with enrichment stage, and from being circulated to oxidation reactor here.In these compositions, solid matter (as aromatic carboxylic acid crystal and catalyzer) and high boiling composition are collected in the bottom of distillation tower, and reaction solvent (as lower boiling aliphatic carboxylic acid) is discharged in higher relatively position.
These fractions so can be back to oxidation reactor again, also can be by the liquid fraction retrieving arrangement being arranged on the bottom of distillation tower, the position recovery lower from distillation tower has the acetate of higher concentration, thereby the fraction that will so reclaim is as aromatic carboxylates's liquid-absorbant, and the slurries that wash reclaiming from oxidation reactor as washings pass through the crystal that obtains after the solid-liquid separation.When reaction stops owing to emergency situation, go out such fraction, can prevent a large amount of withdrawing fluids and import oxidation agent again and the situation of diluting reaction solution from system recoveries.
In enrichment step, the cat head of discharging from the distillation tower top distillates the gas water cooling that is cooled condenser, become condensation product so that be contained in the vapor condensation of discharging in the gas.Condenser can be made of the device of solid memder, or is made of the device that is subdivided into a plurality of attached members again.The temperature of condensation is the temperature that steam can be condensed, and wherein alphatic carboxylic acid ester was both condensable can not be condensed yet.Resulting condensation product or all be directed at membrane separation step, perhaps part is conducted to membrane separation step and makes a part be back to distillation tower.
In membrane separation step, partly or entirely condensation product carries out divided thin film from so that water and byproduct (as alcohol) are penetrated into the permeate side of film, and aliphatic carboxylic acid is concentrated in the enriched material side, thereby they are separated.Separating film for realizing this separation purpose can adopt reverse osmosis membrane.Employed reverse osmosis membrane can be: polymeric amide, aromatic polyamides, polyacrylonitrile, polypropylene, poly-inclined to one side 1,1-difluoroethylene, fluorinated ethylene propylene, polyvinyl alcohol, polyester, polyimide, polysulfones, polyethers inkstone, rhodia, cellulose ester, triacetyl cellulose, polyethers urate, polypiperic azamide, poly-furans (polyfurane) and polymine, wherein preferred reverse osmosis membrane is crosslinked aromatic polyamides.Separating film can be any alternative configuration, comprises plane formula, tubulose, spirrillum and hollow fiber.Use divided thin film from realizing separating the difference that is based on molecular dimension, ionic activity etc., the permeable membrane that is suitable for adopting can make water and byproduct (as alcohol) be penetrated into permeate side, and aliphatic carboxylic acid is concentrated in the enriched material side.The ratio that this film penetrates alphatic carboxylic acid ester is 20%, and the ratio that is retained in the enriched material side is 80%.Can realize that divided thin film is from, but preferred a plurality of stage with the single stage.
Be penetrated into permeate side from, the unnecessary byproduct composition that produces in the oxidizing reaction (as water and alcohol, for example methyl alcohol) by permeable membrane by condensation product being carried out divided thin film, thereby reached isolating effect.Aliphatic carboxylic acid (as acetate) as reaction solvent is retained in the enriched material side, and concentrates therein.If only separating of acetate and water undertaken by distillation, because the boiling point of water approaches the boiling point of acetate, thereby employed distillation tower should have very high height.Yet, by divided thin film from, they since the difference of molecular dimension and ionic activity can easily separate.If it is incomplete separating, divided thin film is from carrying out in the multistage.
Resulting penetrant can be handled so that water and byproduct (as alcohol) are separated in suitable tripping device, and the water of separating can be discharged from system, perhaps is used as washings and washs prepared aromatic carboxylic acid.Enriched material is back to oxidation step again, wherein is preferably the top that part or all of condensation product is back to distillation tower and is beneficial to distillation.
By the condensing temperature of restriction in the condensing steps, alphatic carboxylic acid ester is condensed or transfers to a side of discharging gas.If alphatic carboxylic acid ester will be transferred to discharge gas, in absorption step,, gas and absorption liquid can in absorption liquid, absorb alphatic carboxylic acid ester by being contacted.As absorption liquid, can make water, also can use acetate.Absorption liquid can so be directed at membrane separation step, also can be hydrolyzed through hydrolysing step earlier before it is directed at membrane separation step.
In hydrolysing step, condensation product and/or absorption liquid and/or penetrant and/or enriched material (by divided thin film from being produced) are contacted, so that the alphatic carboxylic acid ester hydrolysis with hydrolyst.Under the situation that adopts atmospheric distillation tower, preferably make the whole penetrant generation hydrolysis of divided thin film from middle generation.As for hydrolyst, can adopt ion exchange resin, preferred highly acid Zeo-karb, especially the macroreticular type of H-type, but also can use by the catalyzer that acid or alkali are formed.
Alphatic carboxylic acid ester will be broken down into corresponding pure and mild aliphatic carboxylic acid, and hydrolysate passes through divided thin film as mentioned above from can separatedly coming.The penetrant that to separate through membrane separation step or enriched material be by hydrolysis treatment, resulting hydrolysate in film separation phase subsequently, carry out divided thin film from; Perhaps enriched material is back to oxidation step,, forms condensation product and be conducted to membrane separation step then through distillation, with this realize divided thin film from.
According to the present invention, can not only realize oxidizing reaction, and the water that forms in the reaction and alcohol also can be by divided thin film from removing, thereby objective carboxylic acid can be from byproduct of reaction (as water and byproduct, as alcohol etc.) in separate effectively and be recovered, also make wastewater treatment become easy simultaneously.
By will distill and divided thin film from combining, even the height of employed distillation tower is not high, aromatic carboxylic acid also can be separated effectively from byproduct of reaction (as water and byproduct, as alcohol etc.) and be recovered, and also makes wastewater treatment become easy simultaneously.
By combining absorption step, alphatic carboxylic acid ester can reclaim from discharge gas through condensing steps.By making alphatic carboxylic acid ester generation hydrolysis reaction, be improved by membrane separation step separation aliphatic carboxylic acid and alcoholic acid efficient.Here, hydrolysing step and membrane separation step are combined make aliphatic carboxylic acid from ethanol, separate easily.In addition, by absorption step and hydrolysing step and membrane separation step are combined, the alphatic carboxylic acid ester that is present in the discharge gas of oxidation can be recovered and be effectively utilized, and has improved the efficient that aliphatic carboxylic acid is separated from ethanol simultaneously.
The technical scheme of invention
By the embodiment of the method that is used to prepare terephthalic acid the present invention is described below with reference to accompanying drawings.
The schema of Fig. 1-3 respectively illustrates the embodiment that the present invention uses the high pressure distillation tower.Fig. 4,5 schema have shown that the present invention uses each embodiment of atmospheric distillation tower.In Fig. 1-3,1 represents oxidation reactor, and the top of oxidation reactor directly links to each other with distillation tower 2 (high pressure distillation tower).3 is condensers, and 4 and 5 all is water cooler, and 6 is absorption towers, and 7 is pumps.8 and 8a represent film separating device respectively with separating film 9 or 9a.10 and 10a represent hydrolysis container respectively with catalyst layer 11 or 11a (forming by ion exchange resin respectively).
In preparing the method for terephthalic acid, embodiment is shown in the schema among Fig. 1-3, in oxidation reactor 1, add the raw material of p-Xylol by pipeline L1 as alkyl-aromatic compounds, add acetate as reaction solvent, add heavy metal compound and bromine compounds as catalyzer, provide air as molecular oxygen-containing gas by pipeline L2 to it, under High Temperature High Pressure, carry out liquid-phase oxidation to form terephthalic acid.Resulting terephthalic acid crystal settling comes out to form slurries and reclaims by pipeline L3.
In Fig. 1, the discharge gas of oxidation is directed at distillation tower 2 under High Temperature High Pressure, and realizes distillation procedure by packing layer 12.Most of solvent and raw material (p-Xylol) are distilled out together, and the fraction that is contained in the catalyzer in the discharge gas of oxidation and contains these compositions (solvent and raw material) is back to oxidation reactor 1.The discharge gas that contains some acetate and lower boiling byproduct (as methyl alcohol etc.) is imported into condenser 3 and cools off, acetate, water, methyl alcohol and other byproduct formation condensation product that is condensed.Part methyl acetate (alphatic carboxylic acid ester) also here is condensed.
The partial condensation thing so is back to distillation tower 2, and wherein a part is collected device 13 collections and discharges by pipeline L4, is sent to the concentration compartments 14 of film separating device 8 after supercooler 4 coolings under the pressurize that pump 7 applies.Impelled by film 9 from, the low-molecular-weight composition of nonionic (as water and methyl alcohol) by divided thin film and to be infiltrated into permeate chamber L5.Penetrant is discharged by pipeline L5, and enriched material is back to the top of distillation tower 2 by pipeline L6.
Import water cooler 5 from the top expellant gas of condenser 3 by pipeline L7, after being cooled, water cooler 5 imports absorption tower 6 again, cooled gas is by packing layer 16, here and from the absorption liquid of pipeline L8 contact, be absorbed in the absorption liquid thereby will discharge methyl acetate contained in the gas.Having removed methyl acetate discharge gas afterwards discharges by pipeline L9.The absorption liquid that has absorbed methyl acetate flows through pipeline L10, and flows in pipeline L4 together with condensation product, so resulting mixture is conducted to film separating device 8.According to the different separation performancies of employed film, methyl acetate or stay the enriched material side perhaps is penetrated into permeate side by separating film, all can be hydrolyzed by suitable technology in both cases.
In the technical scheme of Fig. 2, the hydrolysis container 10 that contains catalyst layer 11 is set at the top of water cooler 5.In this embodiment, contained methyl acetate is hydrolyzed to methyl alcohol and acetate by hydrolysis container 10 from the cooled discharge gas that water cooler 5 is discharged.In absorption tower 6, be recovered by gas is contacted, still be retained in the acetate and the methyl acetate of flowing through in the gas of hydrolysis container 10 with the water that is provided by pipeline L8.When hydrolysate by pipeline L10 with when the condensation product of pipeline L4 enters film separating device 8 together, acetate is retained in the enriched material side, and methanol crossover is to permeate side.Thereby, even in absorption tower 6 with under the situation of acetate as absorption liquid, can reclaim acetate equally and it is delivered to distillation tower 2.Consistent among other structure and operating process and Fig. 1.
In the embodiment of Fig. 3, all enter condenser 3 from distillation tower 2 expellant gas and also here cool off by pipeline L7.Resulting condensation product and the absorption liquid that has absorbed methyl acetate in absorption tower 6 are mixture together and import film separating device 8 by pipeline L10, by divided thin film from various compositions are separated, i.e. acetate, water and methyl alcohol.The part methyl acetate still is retained in the enriched material side, and other parts are penetrated into permeate side.
Penetrant is imported among the hydrolysis container 10a, and here methyl acetate is hydrolyzed to acetate and methyl alcohol by catalyst layer 11a.Hydrolysate in film separating device 8a through divided thin film from, wherein acetate is stayed the enriched material side, the first alcohol and water is penetrated into permeate side.Enriched material in film separating device 8 and 8a is added in together and is directed at hydrolysis container 10 by pipeline L6, the methyl acetate reaction that is hydrolyzed here, and foldback is got back to the top of distillation tower 2 then.In acetate and methanol eddy cycle period to oxidation reactor, the circular treatment of the discharge gas of simultaneous oxidation, acetate and methyl alcohol is separated from one another coming in film separating device 8.
In the embodiment of Figure 4 and 5, the top of oxidation reactor 1 links to each other with an atmospheric distillation tower (as distillation tower 2), a middle oxidizing reaction off-gas condenser 3a and reducing valve 18 of inserting.Distillation tower 2 links to each other with condenser 3.Oxidizing reaction off-gas condenser 3a links to each other with water cooler 5 and absorption tower 6.
For the device by Figure 4 and 5 prepares terephthalic acid, in reactor 1, infeed the raw material of p-Xylol by pipeline L1 as alkyl-aromatic compounds, infeed acetate as reaction solvent, infeed heavy metal compound and bromine compounds as catalyzer, air-supplied by pipeline L2 simultaneously as molecular oxygen-containing gas, liquid phase oxidation reaction takes place under High Temperature High Pressure and form terephthalic acid.The terephthalic acid of Xing Chenging comes out to form slurries with crystal settling and reclaims by pipeline L3 like this.
In the embodiment of Fig. 4, the discharge gas of oxidation imports oxidizing reaction off-gas condenser 3a by pipeline L11 and here is cooled under High Temperature High Pressure.Part condensation product so is back to oxidation reactor 1, and other parts import distillation tower by pipeline L12 through reducing valve 18, and distills by reboiler 17 heating.Import water cooler 5 from oxidizing reaction off-gas condenser 3a expellant gas by pipeline L13, be sent to absorption tower 6 here after cooling off, in the absorption tower, contact during at it, owing to sorption is removed methyl acetate by packing layer 16 with absorption liquid by pipeline L8 input.The resulting discharge gas of methyl acetate that do not contain is by outside the pipeline L9 discharge system.The absorption liquid that has absorbed methyl acetate mixes to pipeline L12 and condensation product by pipeline L10 and is imported into distillation tower 2.
During the distillation of distillation tower 2, be back to oxidation reactor 1 after contained most reaction solvents (being acetate) rectifying in the discharge gas of oxidation.The overhead product that contains surplus acetate and lower boiling byproduct (as methyl alcohol etc.) imports condenser 3 by pipeline L14, makes residual acetic acid, water vapour, methyl alcohol and the cooling of other byproduct here and forms condensation product.Here, a part of methyl acetate (a kind of alphatic carboxylic acid ester) also is condensed.
Condensation product so is sent in the concentration compartments 14 of film separating device 8 under pump 7 applied pressures, goes into permeate chamber 15 thereby the low-molecular-weight material of nonionic (as water and methyl alcohol) carries out divided thin film by permeable membrane 9 from laggard.Penetrant is discharged by pipeline L5, and condensation product is back to the top of distillation tower 2 by pipeline L6.
In the embodiment of Fig. 5, the hydrolysis container 10 with catalyst layer 11 is set at pipeline L5 and has upward saved water cooler 5.In this set, the penetrant that from film separating device 8, comes out by hydrolysis container 10 time, methyl acetate generation hydrolysis with which, the resulting hydrolysate that contains methyl alcohol and acetate is back to the top of distillation tower 2.
Embodiment
Below, will the present invention be described by embodiment.In these embodiments, unless stated otherwise, % and ppm are all by weight.
The comparative example 1
In oxidation reactor shown in Figure 1, p-Xylol is oxidized with the preparation terephthalic acid under 190 ℃ and 1.2Mpa.The discharge gas of oxidation distills in distillation tower 2, is condensed to 160 ℃ in condenser 3.The cat head of distillation tower 2 distillates gas and contacts with a kind of absorption liquid (flow is the water of 10kg/hr) down to absorb methyl acetate wherein at 35 ℃ in resorber 6, the absorption liquid of resulting 50kg/hr and mix from the condensation product (55kg/hr) of condenser is outside the mixed solution discharge system with the 105kg/hr that obtains.Mixed solution contains 1.5% acetate, the methyl acetate of 2650ppm and the methyl alcohol of 1040ppm.The methyl alcohol that contains 0.1ppm (volume) acetate, 1020ppm (volume) methyl acetate and 106ppm (volume) from the absorption tower expellant gas.
Embodiment 1
Comparative example 1 method is made the following changes, the condensation product of the 205kg/hr that comes out from condenser 3 and from the absorption tower absorption liquid of 6 50kg/hr that come out mixes, the mixed solution of the 25kg/hr that obtains under pressure rises to 4.9Mpa, be admitted to film separating device 8 carry out divided thin film from, wherein the enriched material of 150kg/hr is back to distillation tower 2, outside the penetrant discharge system of 105kg/hr.As for separating film, can adopt the reverse osmosis membrane SU-820 (trade mark, Toray Industries, the product of Inc.) that forms by the synthetic film of crosslinked polyamide.Penetrant contains 0.3% acetate, the methyl acetate of 303ppm and the methyl alcohol of 1010ppm.Contain the acetate of 0.1ppm (volume), the methyl acetate of 1530ppm (volume) and the methyl alcohol of 305ppm (volume) from the absorption tower expellant gas.
The device of Fig. 2 is operated as follows, speed with 50kg/hr is delivered to absorption tower 6 with absorption agent water, the hydrolyzed liquid of the 90kg/hr that will obtain after hydrolysis from the water of the absorption of hydrolysis container 10 mixes with condensation product from the 205kg/hr of condenser 3, the mixing liquid of resulting 29kg/hr in film separating device 8, carry out divided thin film from, wherein the enriched material of 150kg/hr is back to distillation tower 2, outside the penetrant discharge system of 145kg/hr.Hydrolyst by the storng-acid cation exchange resin of macroreticular type (Amberlist 15, trademark, of Japan Organo Co. Ltd.) constitutes.Other step is identical with embodiment 1, and penetrant contains the methyl alcohol of 0.5% acetate, 550ppm methyl acetate and 1700ppm.The methyl alcohol that from the expellant gas of absorption tower, contains acetate, 103ppm (volume) methyl acetate and the 1100ppm (volume) of 0.5ppm (volume).
Embodiment 3
The device of Fig. 3 is operated as follows, absorption agent water is sent to absorption tower 6 with the flow velocity of 10kg/hr, and the condensation product after being absorbed arrives hydrolysis container 10 and 10a by pump 7 flow velocity with 900kg/hr when pressure rises to 7.8Mpa by film separating device 8 and 8a.Enriched material through film separating device 8 and 8a pools together with the flow velocity of 650kg/hr and 145kg/hr respectively, resulting mixture is back to distillation tower after by hydrolysis container 10, and is outside the penetrant of 105kg/hr is exhausted from system from the flow velocity that film separating device 8a discharges.Other step is identical with embodiment 2.Penetrant contains 0.1% acetate, 50ppm methyl acetate, 2010ppm methyl alcohol.Contain the acetate of 0.1ppm (volume), methyl acetate and 1050ppm (volume) methyl alcohol of 212ppm (volume) from the absorption tower expellant gas.
The comparative example 2
In oxidation reactor shown in Figure 4, p-Xylol is oxidized with the preparation terephthalic acid under 190 ℃ and 1.2Mpa.The discharge gas of oxidation is cooled with condensation under 120 ℃ in oxidizing reaction off-gas condenser 3a.Expellant gas is cooled to 40 ℃ in water cooler 5 from oxidizing reaction off-gas condenser 3a, and the absorption liquid that constitutes with the water (40 ℃) that by flow velocity is 10kg/hr in absorption tower 6 contacts to absorb methyl acetate wherein, the absorption liquid of resulting 210kg/hr and mix from the condensation product of the 465kg/hr of condenser 3a, the mixed solution of resulting 685kg/hr carries out distillation procedure by reflux ratio 4 in distillation tower 2, outside the distillate of the 105kg/hr that discharges from cat head is exhausted from system.Liquid effluent contains 1.5% acetate, 1.6% methyl acetate and 0.1% methyl alcohol.Contain 0.1ppm (volume) acetate, 500ppm (volume) methyl acetate and 30ppm (volume) methyl alcohol from the absorption tower expellant gas.
Embodiment 4
Comparative example 2 method makes the following changes, the condensation product of discharging from condenser 3 rise to import under the pressure of 4.9Mpa film separating device 8 carry out divided thin film from, discharge from system thereby the condensation product of 525kg/hr is back to the penetrant of distillation tower 2 and 105kg/hr.As for separating film, can adopt the reverse osmosis membrane SU-820 (trade mark, Toray Industries, the product of Inc) that forms by the synthetic film of crosslinked polyamide.Penetrant contains the methyl alcohol of 0.3% acetate, 0.3% methyl acetate and 0.08%.Contain 0.1ppm (volume) acetate, 700ppm (volume) methyl acetate and 50ppm (volume) methyl alcohol from the absorption tower expellant gas.
Claims (9)
1, a kind of method for preparing aromatic carboxylic acid, comprising in the oxidation reactor under the High Temperature High Pressure, making alkyl aromatic compound in reaction solvent, carry out liquid phase oxidation reaction with molecular oxygen-containing gas, be reflected under the oxide catalyst existence and carry out, said reaction solvent comprises a kind of aliphatic carboxylic acid, and comprises: when reaction is carried out by divided thin film from removing water and the alcohol that in oxidizing reaction, forms.
2, the described method of claim 1, wherein this method further comprises the steps:
The oxidizing reaction waste gas that to discharge from oxidation reactor imports distillation tower, perhaps oxidizing reaction waste gas is imported the oxidizing reaction off-gas condenser and the gained condensation product is imported distillation tower, in distillation tower, oxidizing reaction waste gas or described condensation product are distilled, the distillation fraction that will contain reaction solvent simultaneously is back in the oxidation reactor
Gas by cooling distillation cat head in condenser make its condense with form condensation product and
To condensation product carry out divided thin film from, make water and alcohol by film permeation to permeate side, and aliphatic carboxylic acid is still stayed the enriched material side and obtain reclaiming.
3, as the said method of claim 2, wherein this method also comprises an absorption step, and this step comprises that the discharge gas that makes condensing steps contacts with absorption liquid with the absorption alphatic carboxylic acid ester, and the liquid that will so absorb is provided to membrane separation step.
4, as the said method of claim 2, wherein this method also comprises an absorption step, this step comprises contacts with the absorption alphatic carboxylic acid ester oxidizing reaction off-gas condenser expellant gas with a kind of absorption liquid, and the liquid that will so absorb is provided to membrane separation step.
5, as each described method of claim 2 to 4, wherein this method also comprises a hydrolysing step, comprise condensation product and/or absorption liquid and/or divided thin film are contacted with hydrolyst decomposing alphatic carboxylic acid ester from penetrant and/or enriched material, and resulting hydrolysate is conducted to membrane separation step.
6, any one said method in the claim 1 to 4, wherein membrane separation step uses a kind of reverse osmosis membrane to carry out.
7, the said method of claim 5, wherein hydrolyst is a kind of ion exchange resin.
8, any one said method in the claim 1 to 4, wherein condensation product all or part of through divided thin film from and enriched material is back to distilation steps.
9, any one said method in the claim 1 to 4, wherein said divided thin film is from carrying out with a plurality of separation phases.
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JP2000077833 | 2000-03-15 | ||
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KR (1) | KR100404935B1 (en) |
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JP2004089882A (en) * | 2002-08-30 | 2004-03-25 | Mitsubishi Heavy Ind Ltd | Separation apparatus for mixture, separation method using the same and method for producing aromatic carboxylic acid |
JP2015160829A (en) * | 2014-02-27 | 2015-09-07 | 三菱化学株式会社 | Method of producing terephthalic acid |
CN109096089A (en) * | 2018-08-28 | 2018-12-28 | 天津市昊永化工工程有限公司 | The preparation method and its device of terephthalic acid (TPA) |
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2001
- 2001-03-07 KR KR10-2001-0011785A patent/KR100404935B1/en active IP Right Grant
- 2001-03-12 TW TW090105684A patent/TW593261B/en not_active IP Right Cessation
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KR20010091930A (en) | 2001-10-23 |
TW593261B (en) | 2004-06-21 |
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