The catalyst and the using method thereof that are used for the high stability of producing acetic acid by carbonylation method
Technical field:
The present invention is used for catalyst and the using method thereof that the low pressure carbonylation is produced acetic acid, belongs to the catalytic reaction engineering technical field.
Background technology:
Acetic acid is a kind of important Organic Chemicals, be mainly used in products such as producing VAM, aceticanhydride, acetates and monochloroacetic acid, it is the important source material of synthetic fibers, adhesive, medicine, agricultural chemicals and dyestuff, also be good organic solvent, purposes is very widely also arranged in industries such as plastics, rubber, printing.
Twentieth century end of the sixties, the rhodium carbonyl-iodine catalyst system (US 3 769 329) of the solubilities that are used for acetic acid synthesis from methanol carbonylation that the people reported such as F.E.Paulik of U.S. Monsanto company; Because methanol carbonylation there are higher catalytic activity and selectivity, and the reaction condition gentleness, make research and suitability for industrialized production that methanol carbonyl is combined to obtain breakthrough.Passed through the development of decades, the low pressure methanol carbonylation method has become most important synthetic method in the acetic acid industry production.
In carbonylation of methanol synthesis process route, the research of catalyst is an important content.Purpose is to study active high, and good stability is easy to reclaim, and has the novel catalyst system of homogeneous phase and heterogeneous two class catalyst advantages concurrently.Research for many years mainly concentrates on these several aspects of base metal, part, carrier and auxiliary agent, and the purpose of its research is to improve existing activity of such catalysts and stability, reaches the raising reaction rate, increases the purpose of acetic acid productive rate.
In the process of methanol carbonylation, be the catalytic performance of center active specy in order to improve with the rhodium, can transform the structure of catalyst itself.Adopt [RhCl (CO) CPEt3] 2 as people such as J.Rankin, with space-time yield STY (product of moles/liter. hour) bring up to 9.2 (Chem.Commun by 5.0 of [Rh (CO) 2Cl] 2,1997.1835), C.A.Carraz etc. select bidentate type phosphine rhodium complex for use, its STY reaches 13.7 (Chem.commun.2000,1277).In order to make rhodium complex catalyst that better dissolubility be arranged in reaction medium, adding some in the reaction system also is the important content of research work to the material that catalytic reaction has facilitation.This class additive is generally some metal salt compounds.In numerous additive, lithium iodide is one of maximum and the most successful example of report, and BP company adopts lithium compound as auxiliary agent, and rhodium concentration is 640ppm in the reaction medium, and during lithium concentration 5340ppm, its STY is 8 (US 6 130 355).
The rhodium catalyst less stable that Monsanto technology is used when reaction temperature surpasses 200 ℃, just begins to decompose inactivation; When low carbon monoxide pressure of tension and low hydroiodic acid concentration, easily generate the rhodium triiodid precipitation, destroy the synthetic acetic acid reaction of carbonylation.Therefore in process of production except that needs are kept the dividing potential drop of high carbon monoxide, also need add excessive hydrogen iodide, so just greatly increase corrosiveness production equipment to keep the stability of rhodium catalyst.
The industrial exemplary of significantly improving production technology by adding the inorganic salts co-catalyst is a Hoechst Celanese company.The said firm has obtained to be undertaken by the Monsanto carbonylic synthesis technology permission of commercial size production of acetic acid in 1978, and it has been carried out a series of improvement.Early 1980s, the said firm has developed the Processes for Producing Acetic Acid of the low water content of independent intellectual property right, and this technology has been improved the production process of acetic acid widely.The main feature of this technology is promptly by adding inorganic salt compounded of iodine to a higher content, and (US 5001259, EP055618) to reach the effect that improves activity of such catalysts and stability.
Summary of the invention
The objective of the invention is to propose a kind of catalyst of novel producing acetic acid by carbonylation method of the Celanese of being different from technology.The characteristics of this catalyst are not add lithium iodide or only adding under the situation of lithium iodide of lower content, still having excellent stability and activity.
The catalyst that the present invention proposes is the catalyst that a kind of low pressure carbonylation of high stability is produced acetic acid, it is characterized in that: this catalyst is major catalyst with the rhodium, mixture with iodomethane or iodomethane and lithium iodide is a co-catalyst, is stabilizing agent with the ionic liquid; Ionic liquid stabilizer is 1,3-dialkylimidazolium phosphate dialkyl ester ([RR ' im] [DRP]), and R wherein, R ' is the alkyl of carbon number between 1-5, R and R ' are identical or different.
The using method of described catalyst is characterized in that: produce acetic acid by the carbon monoxide carbonylation; The temperature of reaction is controlled at 170-230 ℃, and pressure is controlled at 2.0-4.0MPa; Whole reaction system is hereinafter referred to as liquid reaction medium; 1, the percentage by weight of 3-dialkylimidazolium phosphate dialkyl ester in liquid reaction medium is 0.1-5.0%; The water percentage by weight is 1.0-9.0% in the described liquid reaction medium, and the methyl acetate percentage by weight is 0.1-15.0%, and the iodomethane percentage by weight is 6.0-20.0%, and the lithium iodide percentage by weight is 2.0-16.5%, and all the other are acetic acid; Rhodium catalyst is 200-1800ppm in the concentration of pure rhodium in liquid reaction medium.
The catalyst that the present invention proposes is a kind of catalyst that the low pressure carbonylation is produced acetic acid that is used for of high stability, and this rhodium complex is the activated centre, is co-catalyst with the mixture of iodomethane or itself and lithium iodide, is stabilizing agent efficiently with ionic liquid.Wherein ionic liquid stabilizer is 1,3-dialkylimidazolium phosphate dialkyl ester ([RR ' im] [DRP], wherein R, R ' is the alkyl of carbon number between 1-5, and R and R ' can be the same or different, for example, 1-butyl-3-methylimidazole dimethyl phosphate salt, i.e. [Bmim] [DMP].The use amount of [RR ' im] [DRP] is the 0.1-5.0% of reaction medium gross weight, is preferably 0.5-2.5%.The rhodium carbonyl activated centre of catalyst is specially dicarbapentaborane diiodo-rhodium, and the content of rhodium carbonyl in reaction system is preferably 600-1000ppm in rhodium 200-1800ppm.The content of iodomethane in reaction system is 6.0-20.0%, is preferably 11.0-16.0%.The content of lithium iodide in reaction system is 2.0-16.5%, is preferably 6.5-12.5%.When not adding lithium iodide, can not influence the stability of catalyst.This catalyst is when being used for carbonylation production acetic acid, and the employing methyl acetate is a raw material, and medium is the mixture of acetic acid, methyl acetate and water.Water content is controlled at 1.0-9.0% in the reaction system, is preferably 2.0-5.0%, and methyl acetate content is controlled at 0.1-15.0%, is preferably 2.5-7.5%, and the remaining reaction medium is an acetic acid.The temperature of methanol carbonylation is controlled at 170-230 ℃, is preferably 185-195 ℃.The gross pressure of reactor will be controlled at 2.0-4.0MPa, is preferably about 2.5-3.5MPa.
Poor stability is an open defect of original carbonylation of methanol catalyst, mainly be because original catalytic active center is a dicarbapentaborane diiodo-rhodium anion structure, this structure is under reaction condition, especially unstable under the flash conditions, generate the rhodium triiodid precipitation easily, cause the reduction of production capacity, even the pipeline of obstruction production equipment causes stopping production; Because adopting ionic liquid is stabilizing agent, the stability of this catalyst obviously is better than Monsanto carbonylation of methanol catalyst.The Meng Shan reactivity of the used catalyst of methanol carbonylation process counts about 8mol/ (Lh) with space-time yield (STY), composition and reaction condition through the control catalyst, this activity of such catalysts can reach more than the 30mol/ (Lh), through further optimizing, the potentiality on the activity provide wide space for existing expanding production of commercial plant.Methanol carbonylation itself is a reaction that selectivity ratios is higher, and side reaction mainly is that water and reaction of carbon monoxide generate hydrogen and carbon dioxide owing to contain a certain amount of water in the reactor.The hydrogen that generates is also relatively more active, and it can participate in reaction and generate other accessory substance, such as methane, and acetaldehyde etc.This catalyst be owing to can drop to the water content in the reaction system a quite low level, thereby can improve the selectivity of reaction greatly.
Having of lithium iodide is beneficial to the methyl acetate that keeps higher concentration in the reaction system, can reduce the water content in the process units like this, thereby reduce system loading greatly, not only saved energy consumption, and can also increase the production capacity of equipment greatly.A large amount of lithium iodide co-catalysts are the main improvement with respect to Monsanto house journal technology (i.e. BP technology afterwards) of the AO Plus technology of Celanese company.The use of lithium iodide co-catalyst has improved production efficiency greatly, but the too high meeting of content of iodine brings the increase of iodine consumption in the production, increased production cost to a certain extent, the present invention adopts the ionic liquid stabilizer of ad hoc structure, can not add the consumption of lithium iodide or reduction lithium iodide.
The specific embodiment
Reactor is controlled at the certain reaction temperature, and under agitation, carbon monoxide is blasted reactor by distribution device in gas-fluid, for the carbon monoxide pressure of tension that makes the reactor upper space remains on certain level, need discharge gas continuously from the top of the vapor space of reactor, and control the gross pressure of reactor simultaneously.Utilize a liquid level in the liquid-level controller conditioned reaction device, discharge liquid reacting product continuously, and be transported in the flash vessel.Flash vessel comes back to reactor after iodomethane is separated, and to keep wherein certain iodomethane content, remainder enters the acetic acid separated purification system in downstream, obtains acetate products.Send back in the reactor after the material of flash vessel bottom is discharged, this strand material mainly is acetic acid and mixture of catalysts.Continue each component concentrations in the analysis reactor, and control the concentration range that each component in the reactor is in setting by the turnover logistics.
The above is the basic procedure of reaction system in the continuous reaction apparatus.This flow process is suitable for the acetic acid industry process units, also can be fit to pilot-plant and mold trial device.As long as can keep the steady running of reaction system, just enough be used for the performance of evaluate catalysts.We form different catalyst system and catalyzings emphatically, and different working condition is discussed the influence of catalyst performance.In order more clearly to illustrate technology contents of the present invention, further do some description especially exemplified by several embodiment, but it should be noted that the following examples only constitute explanation of the present invention, and be not construed as limiting the invention.
The reference example:
Catalyst reactor consists of rhodium carbonyl (in rhodium) 450ppm, iodomethane 19wt%, and methyl acetate 10wt%, water 0.5wt%, all the other are acetic acid; 230 ℃ of control reaction temperatures, reaction pressure 3.0MPa.The activity of carbonylation is 6.5mol/ (Lh), and the reaction back finds that a large amount of Powdered rhodium triiodid precipitations is arranged.This reaction just begins to carry out up to 230 ℃.Proof is in the existence of water that does not have high level or lithium iodide, and the stability of this catalyst and activity are all very poor.
Embodiment 1
Catalyst reactor consists of rhodium carbonyl (in rhodium) 450ppm, iodomethane 19wt%, and ionic liquid [Bmim] [DMP] is 5wt%, methyl acetate 11wt%, water 0.5wt%, all the other are acetic acid; 250 ℃ of control reaction temperatures, reaction pressure 3.0MPa.The activity of carbonylation is 10mol/ (Lh), does not find any precipitation after the reaction.This stability that proves this reacting middle catalyst is better.
Embodiment 2
Catalyst reactor consists of rhodium carbonyl (in rhodium) 450ppm, iodomethane 19wt%, and ionic liquid [Mmin] [DMP] is 5wt%, methyl acetate 10wt%, water 0.5wt%, all the other are acetic acid; 250 ℃ of control reaction temperatures, reaction pressure 3.0MPa.The activity of carbonylation is 10mol/ (Lh), does not find any precipitation after the reaction.This stability that proves this reacting middle catalyst is better.
Embodiment 3
Catalyst reactor consists of rhodium carbonyl (in rhodium) 800ppm, iodomethane 15wt%, and ionic liquid [Bmim] [DBP] is 5wt%, methyl acetate 8wt%, water 3wt%, all the other are acetic acid; 180 ℃ of control reaction temperatures, reaction pressure 2.5MPa.The activity of carbonylation is 17.6mol/ (Lh), does not find any precipitation after the reaction.This stability that proves this reacting middle catalyst is with better active.
Embodiment 4
Catalyst reactor consists of rhodium carbonyl (in rhodium) 1000ppm, iodomethane 11wt%, and ionic liquid [EEim] [DEP] is 5wt%, methyl acetate 2.5wt%, water 8wt%, all the other are acetic acid; 180 ℃ of control reaction temperatures, reaction pressure 3.5MPa.The activity of carbonylation is 25.8mol/ (Lh), does not find any precipitation after the reaction.
Embodiment 5
Catalyst reactor consists of rhodium carbonyl (in rhodium) 1000ppm, iodomethane 8wt%, and ionic liquid [Emim] [DMP] is 2wt%, methyl acetate 5wt%, water 3wt%, all the other are acetic acid; 190 ℃ of control reaction temperatures, reaction pressure 3.0MPa.The activity of carbonylation is 23.5mol/ (Lh), does not find any precipitation after the reaction.
Embodiment 6
Catalyst reactor consists of rhodium carbonyl (in rhodium) 1000ppm, iodomethane 8wt%, and lithium iodide 2wt%, ionic liquid [Bmim] [DMP] is 0.5wt%, methyl acetate 10wt%, water 4wt%, all the other are acetic acid; 185 ℃ of control reaction temperatures, reaction pressure 3.0MPa.The activity of carbonylation is 22.7mol/ (Lh), does not find any precipitation after the reaction.
Embodiment 7
Catalyst reactor consists of rhodium carbonyl (in rhodium) 1000ppm, iodomethane 8wt%, and lithium iodide 16wt%, ionic liquid [Bmim] [DMP] is 1wt%, methyl acetate 2wt%, water 2wt%, all the other are acetic acid; 170 ℃ of control reaction temperatures, reaction pressure 5.0MPa.The activity of carbonylation is 20.4mol/ (Lh), does not find any precipitation after the reaction.
Embodiment 8
Catalyst reactor consists of rhodium carbonyl (in rhodium) 1800ppm, iodomethane 8wt%, and lithium iodide 16wt%, ionic liquid [Bmim] [DMP] is 1wt%, methyl acetate 9wt%, water 2wt%, all the other are acetic acid; 170 ℃ of control reaction temperatures, reaction pressure 3.0MPa.The activity of carbonylation is 38.5mol/ (Lh), does not find any precipitation after the reaction.