WO2004056756A1 - Verfahren zur kontinuierlichen herstellung von isocyanaten - Google Patents
Verfahren zur kontinuierlichen herstellung von isocyanaten Download PDFInfo
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- WO2004056756A1 WO2004056756A1 PCT/EP2003/014185 EP0314185W WO2004056756A1 WO 2004056756 A1 WO2004056756 A1 WO 2004056756A1 EP 0314185 W EP0314185 W EP 0314185W WO 2004056756 A1 WO2004056756 A1 WO 2004056756A1
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- phosgene
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C263/00—Preparation of derivatives of isocyanic acid
- C07C263/10—Preparation of derivatives of isocyanic acid by reaction of amines with carbonyl halides, e.g. with phosgene
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C263/00—Preparation of derivatives of isocyanic acid
- C07C263/18—Separation; Purification; Stabilisation; Use of additives
- C07C263/20—Separation; Purification
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C265/00—Derivatives of isocyanic acid
- C07C265/14—Derivatives of isocyanic acid containing at least two isocyanate groups bound to the same carbon skeleton
Definitions
- the invention relates to a process for the preparation of aromatic or aliphatic isocyanates.
- aromatic isocyanates these are preferably methylene di (phenyl isocyanate) (MDI) and tolylene diisocyanate (TDI), and in the case of the aliphatic hexamethylene diisocyanate (HDI) and isophorone diisocyanate (IPDI) or others.
- the aim of the present invention is to develop a two-stage or multi-stage process which gives isocyanates with very high chemical yields and high space-time yields with low phosgene holdup.
- the reaction between organic amine and phosgene is carried out in two or more stages, in an inert solvent, preferably toluene, chlorobenzene, dichlorobenzene or mixtures of the latter, and with an excess of phosgene, characterized in that a reduction of the Pressure takes place and the first phosgenation stage comprises a static mixer, preferably a nozzle, the second stage comprises a residence time apparatus and the third stage comprises a (reaction) column.
- the pressure upstream of the nozzle is preferably 3-70 bar, preferably 15-45 bar.
- the residence time reactor of the second stage is preferably operated at a pressure of 2.5-35 bar, preferably 15-35 bar.
- the first stage reactor usually a static mixer
- the reactor of the third phosgenation stage usually a column, preferably a reaction column, is preferably operated at a pressure of 2-20 bar, preferably 3.5-16 bar.
- pressure is released to the pressure of the third stage reactor by means of a valve or other suitable device. If necessary, a natural pressure drop is sufficient to reduce the pressure.
- a (reaction) column as described, for example, in WO 99/54289 (DE 19817691) is preferably used as the third stage reactor. It is known to produce isocyanates from amines and phosgene. Depending on the type of amines, the reaction is carried out either batchwise or continuously, either in the gas phase or in the liquid phase (W. Siefken. Liebigs Ann. 562, 75 (1949)). The continuous production of organic isocyanates by reaction of primary organic amines with phosgene has been described many times and is carried out on an industrial scale (see, for example, Ullmann's Encyclopedia of Industrial Chemistry, Volume 7 (Polyurethanes), 3rd revised edition, Carl Hanser Verlag, Kunststoff-Vienna, Pp.
- aromatic isocyanates TDI tolylene diisocyanate
- MDI methylene diphenyl diisocyanate
- PMDI polymethylene polyphenylene polyisocyanate
- HDI hexamethylene diisocyanate
- IPDI isophorone diisocyanate
- the first phosgenation stage is usually carried out in a mixing device, preferably a nozzle.
- the second stage of phosgenation comprises both the decomposition of the carbamoyl chloride to the desired isocyanate and hydrogen chloride and the phosgenation of the amine hydrochloride to the carbamoyl chloride.
- the temperature of the second phosgenation stage is generally higher than that of the first.
- Mixing elements can basically be divided into dynamic mixers such as stirrers and turbines and static mixers, rotor-stator systems such as Kenics mixers, shish kebab mixers, SMV mixers and jet mixers such as nozzles or T mixers (Che. Ing. Tech. MS 1708/88, Progress. Ver.technik 23, 1985, 373, Ind. Eng. Chem. Res. 26, 1987, 1184).
- dynamic mixers such as stirrers and turbines and static mixers
- rotor-stator systems such as Kenics mixers, shish kebab mixers, SMV mixers and jet mixers such as nozzles or T mixers
- Known mixing units include, in particular, nozzles such as ring slot nozzle (DE 1792660), ring hole nozzles (DE 3744001), smooth jet mixing nozzles (EP 0065727), fan jet nozzles (DE 2950216), angular jet chamber nozzles (DD 300.168), three-flow nozzles (DD 132340n) (counterflow valve PS 1146872), dynamic nozzles (FR 69428), Venturi mixing nozzles (DE-AS 1175666).
- Inline mixers US 3321283
- centrifugal or reaction mixing pumps EP 0291819)
- tubular reactors US 3226410
- microstructure mixers EP 0928785
- CA 832432 describes the use of sound waves for mixing.
- EP 0830894 describes a mixer reactor for phosgenation of primary amines, in which the inlet for one substance in the axis of the mixing chamber and the inlet for the (at least one) other substance in the form of a plurality of rotationally symmetrical nozzles arranged in relation to the axis of the mixing chamber is formed, each of these nozzles has a displaceable in the direction of the nozzle axis bolt, which can free the nozzle from adhering solids.
- DD 132340 describes a process for the phosgenation of amines to mono-, di- and polyisocyanates under pressure and elevated temperature in the presence of a uniform solvent, an amine-monochlorobenzene mixture and a phosgene-monochlorobenzene mixture being divided into several substreams being fed in parallel to a reactor, a portion of the phosgene-monochlorobenzene mixture being passed centrally and around this central stream of the amine-monochlorobenzene mixture, which in turn is enclosed by a phosgene-monochlorobenzene mixture.
- the polyamine-monochlorobenzene mixture is fed, for example, in a ring at 150 ° C.
- phosgenation reactor Before entering the reactor, the mixture is rotated by an appropriate swirl device.
- a phosgene-monochlorobenzene mixture heated to 150 ° C. is fed into the reactor as the reactant.
- the relative speed between the two reactants is approximately 15 m / s.
- Isocyanates are prepared from the corresponding amines by phosgenation in stirred tanks (for example DE-OS 1468445), in stirred tank cascades (DE-PS 844896), in reaction columns or reaction columns filled with packing elements (for example WO 99/54289) or in unfilled columns (for example Ull anns Encyclopedia of Industrial Chemistry, 4th edition (1977), pages 351 ff).
- a cycle mode of operation is also implemented by using loop reactors in order to create sufficient dwell time for complete conversion with a limited reaction volume (or holdup).
- Isocyanate synthesis is often carried out in the first stage at a very low temperature and in the second at a significantly higher temperature in a residence time apparatus. This procedure is often referred to as cold-hot phosgenation and is described, for example, in W. Siefken, Liebigs Analen der Chemie 562 (1949), page 96.
- a suspension of the intermediates carbamoyl chloride and amine hydrochloride is prepared at low temperature, especially at 0 ° C or room temperature, but at most 60 ° C, which is then converted to the isocyanate in a residence time apparatus at higher temperatures, in particular in the range between 100-200 ° C becomes.
- DE 949227 describes a cold-hot phosgenation process for the continuous production of isocyanates by reacting amines with phosgene in the liquid phase in the presence of a solvent, characterized in that in the cold phosgenation a solution or slurry of the amine in an inert solvent with liquid phosgene or Solution of phosgene in an inert solvent is brought together continuously and without external cooling in a mixing device with intensive stirring and the reaction mixture thus obtained is then subjected to hot phosgenation.
- Turbomixers and centrifugal pumps and generally mixing devices with mechanically moving parts are claimed as the mixing device.
- the residence time in the mixing device is a few seconds to a minute.
- DE 949228 describes a cold-hot phosgenation process for the continuous production of mononuclear aromatic diisocyanates (for example tolylene diisocyanate), a suspension being continuously prepared from the amine on which the isocyanate is based and the total amount of the solvent used in the phosgenation, this suspension continuously with phosgene in the cold, the reaction product then continuously through one or more vertical or inclined pipes, so-called phosgene towers, in which the material, if necessary with supply of gaseous phosgene, to which the phosgenation temperature is heated, and then the solution is freed from dissolved phosgene by gassing with a dry inert gas stream in a column.
- mononuclear aromatic diisocyanates for example tolylene diisocyanate
- O-Dichlorobenzene was used as solvent.
- the cold phosgenation is carried out at 0 ° C. in a stirred tank, then the reaction mixture is preheated to 30 ° C., and finally at 170 ° C. in two phosgenation towers connected in series in the hot phosgenation reaction to give the isocyanate.
- Gaseous phosgene is introduced at the foot of the second phosgene tower.
- the hydrogen chloride / phosgene / solvent mixture drawn off at the top in the two phosgene towers is partially condensed in the respective top condenser of the respective phosgene tower and returned to the sump.
- the non-condensable portion of phosgene and chlorine-hydrogen is fed to a phosgene / hydrogen chloride separation system or to destruction.
- the liquid and completely through-phosgenated reaction product leaving the second phosgene tower runs into a bubble cap column and is freed from the dissolved phosgene by stripping with a nitrogen stream in countercurrent.
- the vapors drawn off at the top are fed to a condenser and the condensed solvent is returned to the top of the column.
- the reaction product is drawn off in the solvent and fed to the distillation.
- a cold-hot phosgenation is also described in DE 952086.
- the hot phosgenation is carried out in vertical reaction towers filled with Raschig rings or other packing elements.
- Cold phosgenation is carried out at 0 ° C and hot phosgenation with an increasing temperature profile from 120 ° C to 160 ° C.
- the circulated solvent is fed to the cold phosgenation stage, not at the lower end of the reaction towers.
- the dilution of the reaction product of the cold phosgenation brings the advantage of a solution with a lower viscosity instead of a viscous suspension of carbamoyl chloride and amine hydrochloride.
- DE 2058032 also describes cold-hot phosgnation.
- the hot phosgenation is carried out in horizontally lying tubular reactors at temperatures of up to about 200 ° C., characterized in that the reaction mixture from the cold phosgenation in the hot phosgenation stage with constant mechanical mixing with a slowly increasing temperature profile. is reacted to.
- Cold phosgenation takes place at a temperature of 0 ° C.
- US 2908703 describes a two-stage process for the preparation of aromatic isocyanates, in which the first reaction step is carried out at a temperature of 60-0 ° C., preferably 70-85 ° C., with chlorobenzene as solvent, and the second reaction step is carried out at a temperature, high enough to decompose the intermediate to the isocyanate.
- a solution of amine in an organic solvent, preferably chlorobenzene or o-dichlorobenzene, and gaseous phosgene are simultaneously introduced into a stirred and heated reactor, so that a saturated phosgene solution is formed and the phosgene excess is at least 50% of the stoichiometric amount of phosgene for the amine phosgene.
- the process described can also be carried out continuously by carrying out the first reaction step in a first and the second in a second reactor.
- the reaction is usually carried out at normal pressure.
- the concentration of the amine in the organic solvent is 2-20% by weight, preferably 5-10% by weight. Higher concentrations lead to the formation of by-products, especially ureas and polyureas.
- DE 2153268 describes a process for continuous cold phosgenation of organic primary amines by reaction with a solution of phosgene in an inert solvent in a multistage, non-self-priming centrifugal pump.
- the centrifugal pump simultaneously conveys the reaction mixture thus obtained to the subsequent hot phosgenation stage.
- the inlet temperature into the pump is -105 ° C to + 25 ° C for the phosgene solution and 50 to 100 ° C for the amine solution.
- the outlet temperature of the reaction mixture is 50 to 110 ° C.
- the concentration of the amine solution is 5 to 40% by weight, that of the phosgene solution 20-65% by weight.
- the amount of phosgene is at least 1 mol, preferably 1.5-3 mol, per mol of amine group.
- EP 0716079 describes the influence of pressure and temperature on the reaction and the excess of phosgene. The lowering of the excess of phosgene at higher temperatures is generally countered by an increased reaction pressure.
- DE-OS 1768439 describes a process for the continuous production of organic isocyanates which is characterized by the combination of high temperature above 180 ° C. and high pressure of 20 to 150 atm and high phosgene concentration in the reaction area. The amount of amine introduced is 2.5 times to 5.5 times the stoichiometric amount. Due to the extremely high pressure and the very high temperature, acceptable space-time yields can still be achieved. The residence time of the reactants in the reaction zone is 5-60 s.
- the preferred solvent is chlorobenzene.
- the disadvantage of the process is the reduced yield and quality due to the increased formation of by-products, especially urea, due to the high temperature.
- large-scale printing equipment is very expensive and problematic because of the high toxicity of the phosgene.
- Carrying out the reaction between amine and phosgene at high pressure also has the disadvantage that, according to Henry's law, the concentration of hydrogen chloride in the liquid phase is increased in addition to the phosgene.
- amine hydrochlorides are undesirable because their phosgenation is very slow according to the current teaching and is therefore the rate-determining step of the overall reaction. This leads to very long dwell times and phosgene holdups.
- EP 0065727 describes a process with a nozzle and tubular reactor.
- the invention relates to a process for the continuous production of organic mono- and polyisocyanates in a one-step reaction by continuously combining solutions of primary mono- or polyamines in inert organic solvents with excess amounts of phosgene dissolved in an inert organic solvent at pressures of 10 to 1000 bar. preferably 25 to 150 bar, and temperatures of 120 to 300 ° C, preferably 150 to 250 ° C in a mixing room and optionally a downstream reaction zone with continuous workup, the excess phosgene solution used continuously in a mixing room and the Amine component used is injected using a smooth jet nozzle.
- the smooth jet nozzle essential for the process has a clear diameter of 0.1-30 mm.
- the molar ratios of phosgene to amino groups are 2: 1 to 30: 1, preferably 3: 1 to 18: 1.
- the post-reaction zone can be a tubular reactor, a tube bundle reactor or, for example, a cascade of stirred tanks.
- the average residence time in the mixing vessel and in the downstream reaction zone is between 5 seconds and 5 minutes.
- the reaction mixture leaving the after-reaction zone is expanded in one or more stages to atmospheric pressure in a pressure relief vessel, as a result of which a temperature drop of 50-150 ° C. occurs.
- the gas and liquid phases are separated in the expansion vessel. Chlorobenzene or o-dichlorobenzene are used as preferred solvents.
- GB 827376 describes a continuous process for the preparation of aromatic isocyanates by reaction of an amine in free form in a solvent or as a salt easily suspended in this solvent, which is easily decomposed to the amine, and a solution of phosgene in an inert solvent at a pressure of greater than 3 * 10 5 Pa, the reactants being introduced simultaneously with mixing into the lower end of a vertical tubular reactor in which the reaction products rise rapidly to the upper end.
- the liquid phase is collected in a container from which it is removed to isolate the isocyanate.
- This container can be a phase separator, which is operated under the same pressure, communicates via an overflow pipe with the liquid outlet and a throttle valve in the Has liquid outlet.
- the liquid separated off in the container is fed to a column which is operated under atmospheric or excess pressure and elevated temperature, as a result of which residual phosgene and hydrogen chloride are separated off overhead in gaseous form.
- the excess phosgene is condensed out (preferably with cooling water) from the hydrogen chloride / phosgene mixture separated off in the container, and the hydrogen chloride separated off in this way is expanded and removed.
- the reactants are fed to the tubular reactor with a common or two separate pumps or else mixed in a Venturi mixing nozzle, preferably with separate inlets for the two reactants, and introduced from there into the tubular reactor.
- the temperature described in the tubular reactor is 80-200 ° C, the pressure is greater than 3 * 10 5 Pa, maximum the vapor pressure of the reaction mixture and preferably 15-20 * 10 5 Pa.
- US 3226410 describes a continuous process for the preparation of aromatic isocyanates by mixing a stream of an aromatic amine into a phosgene stream in a tubular reactor at Reynolds numbers greater than 2100 (preferably 5000-2000000) and temperatures of 60-90 ° C., preferably 80-85 ° C. , described.
- the amount of phosgene is at least 1 mol, preferably 6 to 12 mol, per mol of amine.
- the reaction solution is then, optionally after preheating, transferred to a second reactor, in particular a kettle or a column, which has a temperature of 110 to 135 ° C., preferably 110 to 120 ° C.
- the amine concentration is 2 to 25% by weight, preferably 5 to 10% by weight, the phosgene concentration 10 to 100% by weight, preferably 10 to 60% by weight.
- the pressure at which the phosgene stream is transferred to the tubular reactor is 50-170 psig; the pressure of the amine stream must be higher to prevent back mixing.
- the liquid phase containing isocyanate, solvent, relatively small amounts of by-products, hydrogen chloride and phosgene dissolved in the solvent is drawn off from the second reactor, separately from the gas phase containing hydrogen chloride, solvent, phosgene and traces of the isocyanate.
- Chlorinated hydrocarbons which are inert and have a lower boiling point than the isocyanate are used as solvents. Chlorobenzene is particularly preferred.
- the second reactor at a pressure of 45 psig or higher, is followed by a retention tank and a buffer vessel, from which level control is carried into a column for removing excess phosgene.
- Phosgene, hydrogen chloride and solvent are taken overhead and returned to the phosgene container.
- the bottom product consisting of isocyanate and solvent, is preferably carried out in one stage in the solvent separation by distillation.
- the separated from the isocyanate Solvent is used to absorb the remaining phosgene from the hydrogen chloride stream.
- the phosgene drawn off in the second reactor and in the buffer tank is condensed in two stages and returned to the phosgene tank.
- the uncondensed phosgene / hydrogen chloride mixture is fed into a phosgene absorber, to which the solvent obtained in the solvent separation is applied.
- the unabsorbed gas mainly hydrogen chloride, is then reacted with water in an absorber to form aqueous hydrochloric acid.
- the tubular reactor is said to be constructed as a "plug flow" reactor without deflections, pockets or other internals which can create dead zones in order to prevent solids from settling out.
- the high Renolds numbers and the design of the reactor as a straight tube should lead to the liquid constantly flushing the walls of caking.
- DE 952086 describes a process for the preparation of isocyanates from primary amines or their salts and phosgene, characterized in that the reaction partners in hot phosgenation in the presence of a solvent or diluent are continuously heated from below by an upright or inclined one Pipe conducts. After passing through this first reaction tube, a second, likewise upright, reaction tower can optionally be added to complete the reaction with the addition of further phosgene.
- the advantage of vertical reaction towers, which are filled with Raschig rings or other packing elements to prevent rapid outgassing, is that the rate of isocyanate formation is increased due to the higher phosgene concentration at the lower entry point of the reactants, which is caused by the adjusts the hydrostatic pressure of the liquid column.
- O-Dichlorobenzene is mentioned as the solvent.
- the process is a two-step process with cold phosgenation as the first step and hot phosgenation as the second step. Cold phosgenation is carried out at 0 ° C and hot phosgenation with an increasing temperature profile from 120 ° C to 160 ° C.
- Disadvantages of this method are, on the one hand, the basic weak points of cold / hot phosgenation and, on the other hand, the low pressure that can be achieved. Pressure vessels and control valves can be used to set significantly higher pressures and thus phosgene concentrations in the liquid phase.
- Another disadvantage is the packing used in the tubular reactors, since the solid intermediate products carbamoyl chloride and amine hydrochloride that are formed and precipitated during cold phosgenation are easy to use. blockage and thus lead to low availability of the system.
- DE 2058032 describes a process for the preparation of isocyanates from amines and phosgene in the presence of an inert solvent, the reaction mixture being treated in the cold phosgenation at temperatures of 0 ° C. and then reacted in the hot phosgenation at temperatures of up to about 200 ° C. , wherein the reaction mixture from the cold phosgenation in the hot phosgenation stage is passed through a horizontally extending reaction chamber with constant mechanical mixing with a slowly increasing temperature profile.
- a horizontally lying tube is claimed as the heatable reaction vessel for the hot phosgenation, through which a shaft with tube devices extends in the longitudinal direction and which has separately heatable sections of a jacket heating.
- a natural evaporation evaporator can be arranged at the end of the tubular reactor.
- An arrangement of three U-shaped interconnected reaction tubes is also described (system of communicating tubes). Cold phosgenation is carried out in the first, vertical tube, hot phosgenation in the horizontal tube and degassing, that is the removal of hydrogen chloride and phosgene from the reaction mixture, is carried out in the second vertical tube.
- DE 2747524 describes a continuous process for the production of aromatic isocyanates, in which so much heat is supplied to the reactor that added phosgene does not lead to cooling and, consequently, to caking of the intermediate carbamoyl chloride on the reactor wall.
- a plug flow reactor is described which consists of two coaxial tubes into which the two reactants amine and phosgene are introduced in countercurrent, isolated from each other, in an inert organic solvent and mixed at the end of the inner tube. The backmixing in the loading zone is switched off, which minimizes the formation of by-products.
- the temperature is controlled with a steam jacket to prevent the mixing zone from becoming clogged with the intermediate product carbamoyl chloride.
- Temperatures of 90-140 ° C are required, in general temperatures of 90-200 ° C are given. However, the initial temperature is 60-90 ° C. Practical considerations determine the upper limit of the temperature. 2 atm is given as a convenient pressure.
- the amine concentration in the inert solvent is 2 to 20%, preferably 5 to 10%. Dichlorobenzene is preferred as the inert solvent.
- a tubular reactor is also the preferred apparatus in the process described in 5 WO 96/16028 for the production of isocyanates with isocyanate as solvent.
- WO 96/16028 describes a continuous, one-step process in which the primary amine, optionally dissolved in an inert, organic solvent, with phosgene, which is 10-60% by weight in the isocyanate,
- the temperature of the first stage is usually 40 to 150 ° C, preferably 60 to 130 ° C, particularly preferably 90 to 120 ° C.
- nozzles are used as static mixers for the first stage.
- a column in particular a reaction column with predominantly ⁇ 10 theoretical plates, is particularly preferably used in addition to stirring machines and cascade tanks. It is particularly advantageous here to operate them in countercurrent.
- the bottom temperature of the column is preferably 80 to
- the column head pressure is preferably 1.0 to 4.7 at (Ü), particularly preferably 2.0 to 3.7 at (Ü).
- a disadvantage of this process is that the amine hydrochloride phosgenation and the carbamoyl chloride decomposition are carried out in one and the same reactor, which leads to longer residence times and higher phosgene holdups.
- US 3544611 describes a process for the production of organic isocyanates at high pressure of 10 to 50 bar. Surprisingly, it was found that carrying out the reaction at higher pressures of at least 10 atm leads to higher yields of isocyanate. Furthermore, the hydrogen chloride / phosgene separation is facilitated by higher pressures.
- the first reaction step of isocyanate production the reaction between amine and phosgene to the intermediate product carbamoyl chloride, is carried out in a loop reactor (mixing circuit).
- the second reaction step the decomposition of the carbamoyl chloride to the isocyanate, takes place in a reaction column downstream of the mixing circuit, a hydrogen chloride / phosgene mixture being obtained at the top of the column.
- phosgene is condensed out in two stages.
- the condensed phosgene is returned to the top of the column.
- Phosgene is removed from a liquid discharge in the rectifying section of the column and fed back to the reaction (the mixing circuit).
- the residual phosgene is removed from the reaction mixture, which is removed at the bottom of the reaction column, in a further column. In the latter, phosgene is taken overhead, condensed in two stages analogously to the first column and returned to the mixing circuit for the reaction. The reaction to the isocyanate is completed in the reaction column.
- DE 3736988 describes a continuous process for the preparation of organic mono- or polyisocyanates in a one-step reaction by reacting the amine dissolved in an organic solvent with phosgene dissolved in an organic solvent in a reaction column at a temperature below 150 ° C.
- the reaction mixture is continuously passed through the reaction column from bottom to top.
- the reaction column has at least 10 chambers separated from one another by perforated plates.
- the concentration of the amine in the inert solvent is 5-40% by weight, preferably 7-20% by weight.
- Preferred solvents are chlorobenzene or dichlorobenzene or mixtures thereof.
- Phosgene is used as a 30-65% by weight, preferably 40-65% by weight, solution in the inert solvent.
- the equivalent ratio of amine to phosgene is 1: 1.5 to 1: 7, preferably 1: 2 to 1: 5.
- the temperature at the top of the column is preferably 70-130 ° C, particularly preferably 90-125 ° C, maximum 150 ° C.
- the average residence time in the reaction column is a maximum of 120 minutes, preferably a maximum of 60 minutes.
- the pressure in the column is 1.2-3 bar abs, preferably 1.5-2.5 bar abs.
- DE 3744001 also uses a perforated plate column with> 10 perforated plates, preferably 20-50 perforated plates, with a residence time of max. 120 minutes, preferably a maximum of 60 minutes, and liquid velocities of 0.05-0.4 m / s, preferably 0.1-0.4 m / s, and gas velocities of 2-20 m / s, preferably 3.5-10 m / s, suggested.
- the horizontally installed perforated floors form 10-50 chambers.
- the top temperature of the reaction column is below 150 ° C, preferably 70-130 ° C, particularly preferably 90-125 ° C.
- the top pressure of the column is 1.2-3 bar (abs.), Preferably 1.5-2.5 bar (abs.).
- a mixing nozzle is required for the first phosgenation stage.
- EP 0291819 describes a two-stage process for the preparation of isocyanates after cold-hot phosgenation, a mixer with a rotor disk being used for cold phosgenation, and preferably using phosgene towers for hot phosgenation.
- the phosgene towers are operated at normal pressure or slightly positive pressure of up to 1.5 atm. It is particularly advantageous to let the cold phosgenation reaction mixture leaving the mixing device enter a heatable tower continuously from above or below and to complete the reaction by adding heat.
- Several towers can be connected in series or a combination of towers and boilers can be used to set a specific temperature profile.
- organic isocyanates from primary organic amines and phosgene are continuously produced in an inert organic solvent in one or more reaction vessels containing fillers, through which co-current flows, in the so-called transition flow.
- the transition flow consists of an amine-containing, liquid organic phase and a phosgene-containing gas phase.
- the reaction takes place at reaction temperatures between 50 and 220 ° C. If the conversion is incomplete, the reaction mixture is circulated several times through the column filled with packing.
- a disadvantage of this process is the high susceptibility to clogging of the packed column, which is caused by solids such as carbamoyl chloride, amine hydrochloride, which are deposited on the packed beds. Urea is caused.
- packed columns are characterized by a high pressure drop, which results in high bottom temperatures and thus a high thermal load on the reaction mixture and the isocyanate formed, resulting in increased by-product formation and reduced yield.
- reaction of phosgene and amine is carried out in a loop reactor or circulation reactor, in which, in addition to the feed streams from amine and phosgene, optionally in
- reaction mixture a solvent, at least part of the reaction mixture is recycled. This dilution by recycling the reaction mixture formed is mainly used for temperature control or better heat dissipation for setting lower temperatures.
- the reaction between amines and phosgene is very exothermic.
- the dwell times are 10 to 180 minutes.
- the molar ratio of amine to phosgene is such that 1 to 10 mol, preferably 1.3 to 4 mol, of phosgene are present in the reaction mixture per amino group.
- EP 0150435 further developed. The process of continuous
- DE 3403204 describes a process for the continuous production of organic isocyanates, preferably polyisocyanates, by reacting organic amines, preferably polyamines, with
- the phosgene is circulated together with the solvent in a tubular circulation line and the amine is mixed into it (mixing circuit).
- the dwell time in the first stage is 30-120 minutes and in the second stage 10-120 minutes.
- Ortho-dichlorobenzene is chosen as the solvent.
- the reaction pressure is preferably at least 1.8-14 * 10 5 Pa, preferably 4.2 * 10 5 Pa or 3.5 * 10 5 Pa.
- the reaction temperature is preferably 102-130 ° C and for toluenediamine preferably 90-120 ° C.
- the phosgene excess is 50-200%, preferably 70%.
- reaction mixture is removed again for the pumping circuit or partially discharged for the solvent separation and pure recovery of the isocyanate.
- the solvent is condensed out in a condenser and returned to the reservoir.
- the preferred pressures in the pump line are 5-20 pounds per square inch.
- the amine concentration in the solvent is 5-30% by weight, the amount of phosgene is at least 1.25 mol per amino group of the amine.
- the preferred solvent is ortho-dichlorobenzene.
- US 3574695 describes an improved continuous process for the production of organic isocyanates.
- the residence times can be shortened by treating the product from the first reaction zone in the second with at least 0.75 mol of phosgene per equivalent of organic amine which was added in the first reaction zone.
- the dwell time in this two- th reaction zone is 5-45 minutes at a temperature of at least 130 ° C.
- a gaseous mixture of hydrogen chloride and phosgene and a liquid solution of the organic isocyanate in the solvent are drawn off continuously from the second reaction zone.
- GB 1034285 describes a continuous process for the preparation of organic isocyanates by reaction of phosgene with a primary polyamine in the presence of an inert organic solvent, the reactants being fed separately into one another and brought into contact in a tubular reactor, and through which a tubular reactor Mix of the same solvent, the reaction mixture and of phosgene is recycled.
- An interconnection of two cylindrical containers, between which the reaction mixture is circulated, or an annular tubular reactor can be used as the reactor.
- the reaction mixture can be stirred using stirrers.
- the temperature in the tubular reactor is 8-50 ° C.
- the pressure is atmospheric or slightly above.
- the concentration of the primary polyamine added in the solvent is 2-20% by weight.
- the amount of phosgene added to the pumping stream is 5 to 20 mol phosgene per mol amine groups in the added polyamine solution.
- Chlorobenzene or ortho-dichlorobenzene is used as the inert organic solvent.
- GB 1212249 describes a process for the preparation of isocyanates in which, in the first stage, an excess of phosgene is reacted with a forward-mixed film of the amine in an inert solvent. A cylindrical tube is considered suitable for producing this film.
- JP 57-048954 describes a process for the preparation of organic isocyanates in which the solution of a primary amine is fed shortly before the feed point of a static mixer which is located in a circulation reactor. A solution of phosgene in organic isocyanate circulates in the circulation reactor.
- the low temperatures in the first stage and the high temperatures in the second stage are energetically disadvantageous in the loop reactor or mixing circuit processes. Since the reaction between see an organic amine and phosgene is strongly exothermic, must be cooled strongly in the first step in order to maintain the desired reaction temperature. The second reaction, the decomposition of the carbamyol chloride to the isocyanate, is clearly endothermic, so that in the second stage the reaction mixture has to be heated again.
- reaction mixture is circulated at a temperature of 60-100 ° C. in a bubble column.
- the process described is carried out at slightly reduced or slightly increased pressure, generally at 0.5-5 bar, preferably at 1-3 bar.
- EP 0570799 describes a process in which the reaction between amine and phosgene to form the isocyanate is carried out in the gas phase.
- Gas phase phosgenation is known for the production of aliphatic diisocyanates (EP 0289840), aromatic diisocyanates (EP 0570799), cyclic diisocyanates (EP 1078918) and triisocyanates (EP 0749958).
- EP 0749958, EP 0676392 and EP 0289840 describe processes for the production of aliphatic di- and triisocyanates by gas phase phosgenation, in which the mixing of the rectands by means of nozzles or a combination of nozzle and annular gap between nozzle and tube at the entry into the described tube reactor he follows.
- a key criterion for mixing is a Reynolds number of RE> 4700 in the tube.
- a jet mixer is specified in EP 0570799 for the production of aromatic diisocyanates by gas phase phosgenation.
- DE 1192641 describes a process for the preparation of isocyanates by reacting primary aromatic or araliphatic amines with phosgene in the presence of solvents and then heating the reaction mixture, using the isocyanate as solvent, which is to be prepared in the reaction.
- DE 100 27 779 claims a process for the preparation of isocyanates by reacting amines with phosgene, in which the isocyanate is used as solvent and the reaction is carried out in a reaction column, the condensed phase at the bottom of the reaction column in whole or in part is fed back into the reinforcement line of the reaction column.
- the theoretical number of plates of the reaction column is 5-60.
- the temperature is -20 ° C to 300 ° C and the absolute pressure 0.2-60 bar.
- US 2683160 describes a process for the preparation of aromatic isocyanates in which gaseous phosgene and a solution of an aromatic amine in a chlorinated aromatic hydrocarbon as solvent simultaneously with a solution of the desired isocyanate in the above. Solvents are given. The solution of the desired isocyanate in the solvent is kept at the boiling point of the solvent, i.e. at a temperature between 130 ° C and 300 ° C, the solution boiling under reflux. The by-product hydrogen chloride and excess, unreacted phosgene are continuously removed via the reflux condenser. The excess phosgene is at least 50%, preferably 80 to 100% of the stoichiometric amount. The amine concentration in the solvent is 5 to 30%, preferably 8 to 12%. The reaction is carried out in a single apparatus which is stirred well and heated sufficiently.
- DE 2252068 describes a process for the production of organic isocyanates from amine and phosgene, the amine preheated to a temperature below its decomposition temperature at superatmospheric pressure first with preheated phosgene in the presence of an excess of an organic isocyanate as solvent at such temperatures and pressures implemented that the reaction takes place in a homogeneous, liquid phase and then in a second stage the internally formed organic carbamoyl chloride is thermally split at a lower pressure.
- the first reaction stage is carried out adiabatically.
- the reaction components are fed in at temperatures in the range of 120-180 ° C.
- the temperature of the reaction mixture at the outlet is kept at 180-250 ° C and the pressure at 100-300 atm.
- the residence time of the components in the first reaction zone should be 5-150 seconds.
- the second reaction stage is carried out isothermally.
- the feed temperature is 120-250 ° C, the pressure 3-30 atm.
- the dwell time is 3-30 minutes.
- the isocyanate drawn off from the second stage is cooled to 50-80 ° C. before being recycled.
- US 3801518 describes a process for the preparation of tolylene diisocyanate with an increased acidity of 0.03-0.3% by weight. This is done by phosgenation of toluenediamine and subsequent residence of the reaction product in a phosgene atmosphere at 100-200 ° C for a period of at least 0.08 hours, preferably 0.08 hours to 2 hours.
- GB 1196008 describes a continuous process for the preparation of aromatic mono- or diisocyanates by phosgenation of the corresponding amines in an organic solvent at a temperature of 120-200 ° C. in two coupled reaction vessels, the phosgene excess being 5-20% in comparison to the calculated stoichiometric amount.
- the aim of the present invention is to develop a two-stage or multi-stage process which gives isocyanates with very high chemical yields and high space-time yields with low phosgene holdup.
- the second reaction the phosgenation of the amine hydrochloride
- High pressures are therefore favorable for this reaction because high pressures imply high phosgene concentrations in the liquid phase.
- elevated temperatures are favorable for achieving high space-time yields.
- DE 3323882 describes a continuous process for the hot phosgenation of amine hydrochloride suspended in solvents or mixtures thereof with carbamoyl chloride with excess phosgene at a temperature between 80 ° C. and 200 ° C., preferably between 100 ° C. and 180 ° C.
- the process is characterized in that the solids are retained in the reactor with the aid of a suitable separation device and the isocyanate formed in the solvent during the reaction is continuously withdrawn from the reactor.
- the solids are preferably separated off using a filter.
- DE 2404773 describes a process for the preparation of mono-, di- and / or polyisocyanates from organic primary amines and phosgene, the primary amines being mixed with at least 3 mol of phosgene per amino group in the absence of a solvent, the reaction mixture simultaneously reacting to a average particle size of 1-100 microns is crushed, and the resulting suspension of carbamic acid chloride and amine hydrochloride in phosgene at temperatures from 100 to 180 ° C, preferably 120 to 160 ° C and pressures of 14 to 55 bar, preferably 21 to 41 bar in the corresponding isocyanates transferred.
- the process is a two-stage process, in the first stage the starting materials primary amine and phosgene at temperatures from -30 ° C. to 60 ° C., preferably 0-50 ° C., at normal pressure or preferably at elevated pressure, in particular at 14 to 55 bar, mixing and at the same time crushing the particles to an average particle size of 1 to 100 ⁇ m, preferably 1 to 50 ⁇ m.
- the amine is added to the phosgene as a liquid, melt or optionally as a powder.
- Various mixing and crushing devices are described.
- the second stage comprises the reaction of amine hydrochloride with phosgene to carbamoyl chloride and its decomposition into isocyanate and hydrogen chloride in a pressure vessel at temperatures of 100-180 ° C, preferably 120 to 160 ° C, and pressures of 14-55 bar, preferably 21 to 41 bar.
- This process is technically very complex and not economical.
- DE-OS 156844 also describes a phosgenation of an amine hydrochloride suspension, which is carried out in a multi-stage stirred tank cascade at elevated temperature.
- the main disadvantage of a cascade of stirred tanks is the high phosgene holdup.
- the invention thus relates to a process for the preparation of polyisocyanates by reacting organic amines with phosgene, characterized in that the reaction takes place in at least three stages, the first stage in a mixing device, the second stage in at least one residence time apparatus and the third stage is carried out in at least one material separation apparatus and the pressure in each subsequent stage is lower than in the previous stage.
- the reaction between organic amine and phosgene is carried out in three or more stages, in an inert solvent, preferably toluene or chlorobenzene, dichlorobenzene or mixtures thereof, and with an excess of phosgene, the pressure being reduced over each of the stages.
- the first phosgenation stage comprises a static mixer, preferably a nozzle.
- the pressure upstream of the nozzle is preferably 3 to 70 bar, in particular 15 to 45 bar.
- the pressure difference across the nozzle is at least 0.5 bar.
- the temperature in the first stage is preferably 80 to 190 ° C., in particular 90 to 150 ° C.
- the second stage comprises one or more residence time devices, preferably a residence time device, which is operated at a pressure of 2.5 to 35 bar, preferably 15 to 35 bar. Behind the nozzle, pressure is released from the second stage by means of a fitting or other suitable device. However, the natural pressure loss of the nozzle can also be used to reduce the pressure.
- the first stage reactor can also be integrated into the second stage reactor.
- a mixing nozzle can be immersed in the gas phase or preferably in the liquid phase of the second reactor, i.e. are wholly or partly in it. It is also possible to discharge the nozzle into the gas or preferably the liquid phase of the second stage reactor using a pipeline, a dip tube or an insertion tube.
- the temperature of the second stage is 80 to 190 ° C, preferably 90 to 150 ° C.
- the reactor type for the second stage tubular reactors, stirred tanks, non-stirred residence devices, phase separation devices and other devices come into consideration.
- the reactor can also be provided with a pumping circuit, which in turn can contain a heat exchanger for adjusting the reactor temperature.
- a heat exchanger for adjusting the reactor temperature.
- the liquid phase is preferably level-controlled and the gas phase is depressurized into the reactor in the third stage.
- the gas phase mainly comprising phosgene, hydrogen chloride and optionally solvent
- the residence time reactor of the second stage can be characterized by larger dimensions and volumes, which can be disadvantageous from a cost or safety point of view, such as phosgene holdup at high pressure.
- the reactor of the second stage can also by two or more identical or different reactors and reactor types can be connected in parallel or, if necessary, also in series to influence the dwell time spectrum.
- the reactor of the third stage of the process according to the invention is operated at a pressure of 2 to 20 bar, preferably at 3.5 to 16 bar. After the residence time reactor of the second stage, pressure is released to the pressure of the third reactor via a fitting or other suitable device. If necessary, a natural pressure drop can also be used.
- the pressure of the subsequent stage should be chosen so that it is lower than that of the previous stage.
- the temperature of the third stage is 80 to 190 ° C.
- a column in particular a reaction column, as described for example in WO 99/54289, is used as the reactor type for the third reactor.
- the bottom temperature is 80 to 190 ° C and the head temperature 50 to 120 ° C.
- the column used as the third stage reactor can also be used to remove the excess phosgene from the reaction mixture.
- the third stage reactor like the second stage reactor, may also be disadvantageously large. In this case, the reactor of the third stage can also be realized by two or more identical or different columns which are connected in series.
- the bottom discharge from the reaction column is worked up using the customary methods for removing any phosgene still present and for separating off the solvent.
- the raw TDI is then subjected to high boiler removal and pure distillation. Phosgene, hydrogen chloride and, if appropriate, solvent are separated off from the vapors of the reaction column and, if appropriate, the residence time reactor of the second stage and, if appropriate, recycled.
- Preferred solvents are chlorinated aromatic hydrocarbons such as dichlorobenzene, chlorobenzene, trichlorobenzene or mixtures thereof, aromatic or aliphatic hydrocarbons such as toluene, xylene, benzene, pentane, hexane, heptane, octane, cyclohexane, biphenyl, ketones such as 2-butanone, methyl isobutyl ketone, Esters such as diethyl isophthalate, ethyl acetate, butyl acetate, nitriles such as acetonitrile and sulfolane are used.
- chlorinated aromatic hydrocarbons such as dichlorobenzene, chlorobenzene, trichlorobenzene or mixtures thereof
- aromatic or aliphatic hydrocarbons such as toluene, xylene, benzene, pentane, hexane, h
- the advantage of the process according to the invention lies in particular in the fact that, in contrast to the processes customary according to the prior art, the two reaction steps 1) phosgenation of the amine hydrochloride to carbamoyl chloride and 2) decomposition of the carbamoyl chloride to isocyanate and hydrogen chloride partly or entirely in separate stages or reactors are carried out, with the mutually independent setting of the optimum pressure and temperature for the respective reaction and the choice of the cheapest reactor design in each case very high chemical yields, very high space-time yields and at the same time a very low one Phosgene holdup can be achieved.
- the synthesis can be carried out adiabatically or isothermally. Due to the different apparatus design, the conditions of the two reactions are optimally taken into account.
- phosgenation of the amine hydrochloride requires high pressures, low pressures are advantageous for the decomposition of the carbamoyl chloride. Furthermore, shorter residence times can be selected for the phosgenation of the amine hydrochloride than for the decomposition of the carbamoyl chloride, which significantly reduces the overall phosgene holdup. Furthermore, the removal of the gaseous hydrogen chloride formed, in particular by stripping, is advantageous for the decomposition of the carbamoyl chloride, because this favorably shifts the carbamoyl chloride-isocyanate equilibrium to the side of the desired isocyanate. This can be taken into account by choosing a (reaction) column as the optimal reactor design.
- the excess phosgene can also be removed at the same time. This is not absolutely necessary in this stage, but can also be carried out in a further stage. Removing hydrogen chloride in the second stage residence reactor, on the other hand, would be very disadvantageous since, together with the hydrogen chloride, this would also remove the phosgene required for the phosgenation of the amine hydrochloride. Evaporating phosgene also led to a cooling of the reaction mixture, which could lead to massive precipitation of solid carbamoyl chloride and amine hydrochloride.
- the fast reaction between amine and phosgene to carbamoyl chloride and hydrogen chloride as well as to amine hydrochloride requires high pressures for good chemical yields due to low by-product formation as reaction conditions of the first and second stage in order to achieve high phosgene concentrations in the liquid phase and thus high phosgene excesses.
- good mixing is required, ie a static mixer, preferably a nozzle, should be used as the apparatus. Height Admission pressures in front of the nozzle allow high pressure losses via the nozzle and thus the introduction of large mixing energies.
- Dissolved amine hydrochloride and very small amine hydrochloride particles react surprisingly very quickly with phosgene in the second stage residence reactor and therefore do not require a long residence time.
- High phosgene concentrations are advantageous here. Higher pressures do not adversely affect the phosgenation of the amine hydrochloride, so that high phosgene concentrations in the liquid phase can preferably be set by higher pressures.
- a pipe reactor, a stirred tank, a non-stirred residence time apparatus, a phase separation apparatus or another residence time apparatus are particularly suitable as apparatus. Heatable versions of these apparatuses are also advantageous in order to compensate for any temperature drops caused by the endothermic decomposition of the carbamyl chloride.
- the reaction of the third stage is a pressure-dependent equilibrium reaction. It is shifted favorably to the side of the desired isocyanate by low pressures. Since this reaction does not require any phosgene, the low phosgene concentrations in the liquid phase, which are characteristic of low pressures, do not interfere, on the contrary, they lead to a low phosgene holdup in the reactor of the third stage, which is favorable from a safety point of view.
- the phosgene holdup can thus be significantly reduced overall in the process, but possibly also in the individual apparatus, in comparison to a stirred tank cascade or a reaction tower.
- the phosgenation of the amine hydrochloride does not have to be completed in the second stage, and the decomposition of the carbamoyl chloride can also begin in the second stage.
- the high pressure required for the phosgenation of the amine hydrochloride causes a low conversion of the carbamoyl chloride to the isocyanate and thus long residence times.
- a high phosgene concentration and long residence times in turn mean a very high phosgene holdup. This is also the case at safety-critical high pressures and temperatures.
- the process can be carried out in all stages at elevated temperature and, if appropriate, isothermally.
- high space-time yields and thus low phosgene holdups and smaller apparatuses with higher chemical yields are achieved, especially in comparison to classic cold / hot phosgenation.
- Avoiding the cooling of the reaction mixture in the first stage and subsequent reheating in the second stage and the subsequent stages also saves a considerable amount of energy.
- long residence times which can only be achieved in part by the cycle mode (loop reactors), can be avoided.
- the circulatory procedure also has a lower phosgene holdup than, for example, a stirred tank cascade, but is characterized by the increased formation of by-products, especially ureas.
- the amine or isocyanate concentration must be kept low, which leads to very low space-time yields.
- the temperatures and pressures used are partly dependent on the amine used.
- the excess phosgene to be used and residence times in the individual apparatus depend on the amine used.
- the excess phosgene should be with diphenyl methane diisocyanates (MDI) and / or polyphenylene polymethylene polyisocyanates (PMDI) or mixtures of these two are at least 100% of the stoichiometric use, for tolylene diisocyanate (TDI) at least 300% of the stoichiometric use, and for hexamethylene diisocyanate (HDI) and isophorone diisocyanate (IPDI) are also at least 300% of the stoichiometric use.
- MDI diphenyl methane diisocyanates
- PMDI polyphenylene polymethylene polyisocyanates
- HDI hexamethylene diisocyanate
- IPDI isophorone diisocyanate
- the dwell time in the first stage is naturally very short and defined by the design of the apparatus.
- the average residence time in the second stage residence apparatus can be between one second and 30 minutes. Average residence times of 30 seconds to 10 minutes are preferred, and average residence times between 2 and 7 minutes are particularly preferred.
- the mean residence time in the apparatus of the third stage depends on the number of separation stages or trays, the weir height, the bottom volume, the load on the column, and other process parameters. It is preferably a maximum of 1 hour.
- the amine concentration in the inert solvent also depends on the amine used and on the solvent. In the case of diphenylmethane diamine (MDA) and / or polyphenylene-polymethylene-polyamines (PMDA) or mixtures of these two, it can be 5-50% by weight, preferably 25-40% by weight, for toluenediamine (TDA) 5-50% by weight %, preferably 15-30% by weight, in the case of hexamethylene diamine (HDA) 5-50% by weight, preferably 15-30% by weight and isophorone diisocyanate (IPDI) also 5-50% by weight, preferably 15 -30% by weight.
- the phosgene concentration in the inert solvent can be 0-70% by weight, preferably 10-50% by weight.
- the same solvent is preferably used as for the amine. There is also no need for a solvent at all.
- a solution of 0.73 kg / h toluenediamine (TDA) in 3.3 kg / h chlorobenzene was reacted in a mixing nozzle with 6.2 kg / h phosgene at a temperature of 110 ° C.
- the pressure drop across the nozzle was 6 bar.
- the reaction mixture was directly in a tubular reactor heated with a double jacket as a residence apparatus with a residence time of 2 minutes at a temperature of 110 ° C. and a pressure of 15 bar abs. relaxed.
- the discharge from the tubular reactor was released into a bubble cap column (reaction column) via a control valve.
- the bottom temperature of the reaction column was 150 ° C, the top pressure 3.5 bar abs.
- tion mixture was directly in a tubular reactor as a residence apparatus with a residence time of 10 seconds at a temperature of 120 ° C and a pressure of about 15 bar abs. relaxed.
- the discharge from the tubular reactor flowed directly into a bubble tray column.
- the bottom temperature of the reaction column was 150 ° C.
- the residence time reactor was a stirred tank which was brought to a temperature of 140 ° C. via the double jacket.
- the stirrer speed was 1000 revolutions per minute.
- the nozzle was also placed outside the residence time reactor and the discharge of the nozzle was led directly into the liquid phase via an insertion tube.
- An expansion into the gas phase led to somewhat lower yields of tolylene diisocyanate (TDI).
- TDI tolylene diisocyanate
- the 5 liquid phase is level-controlled and the gas phase is driven under pressure from the residence time reactor into a bubble cap column (reaction column).
- the stirred kettle was abs in the pressure range between 2.5 and 35 bar. operated.
- the average residence time of the liquid phase (regulated by the level) was up to 30 minutes.
- the stirred tank was also operated with an external loop with a heat exchanger (pump circuit with gear pump).
- the bottom temperature of the reaction column is 110 ° C., the top pressure 3.5 bar abs.
- a mixture 5.0 kg / h
- phosgene 4.0 kg / h, 20% by weight
- hydrogen chloride 0.85 kg / h
- Toluene diisocyanate (1.0 kg / h, 19% by weight), chlorobenzene (3.1 kg / h, 59% by weight), phosgene (1.15 kg / h, 22% by weight), hydrogen chloride ( 0.02 kg / h, 0.3 wt .-%) and small amounts of high boilers (0.02 kg / h, 0.4 wt .-%) deducted.
- chlorobenzene 3.1 kg / h, 59% by weight
- phosgene (1.15 kg / h, 22% by weight
- hydrogen chloride 0.02 kg / h, 0.3 wt .-%)
- small amounts of high boilers (0.02 kg / h, 0.4 wt .-%) deducted.
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Abstract
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Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
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DE50313194T DE50313194D1 (de) | 2002-12-19 | 2003-12-13 | Verfahren zur kontinuierlichen herstellung von isocyanaten |
JP2004561288A JP4324558B2 (ja) | 2002-12-19 | 2003-12-13 | イソシアネートの連続製造方法 |
US10/539,802 US7851648B2 (en) | 2002-12-19 | 2003-12-13 | Method for the continuous production of isocyanates |
ES03789262.7T ES2353005T5 (es) | 2002-12-19 | 2003-12-13 | Método para la producción continua de isocianatos |
AU2003293871A AU2003293871A1 (en) | 2002-12-19 | 2003-12-13 | Method for the continuous production of isocyanates |
AT03789262T ATE484492T1 (de) | 2002-12-19 | 2003-12-13 | Verfahren zur kontinuierlichen herstellung von isocyanaten |
EP03789262.7A EP1575904B2 (de) | 2002-12-19 | 2003-12-13 | Verfahren zur kontinuierlichen herstellung von isocyanaten |
MXPA05006058A MXPA05006058A (es) | 2002-12-19 | 2003-12-13 | Metodo para proteccion continua de isocianatos. |
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DE10260082A DE10260082A1 (de) | 2002-12-19 | 2002-12-19 | Verfahren zur kontinuierlichen Herstellung von Isocyanaten |
DE10260082.1 | 2002-12-19 |
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US (1) | US7851648B2 (de) |
EP (1) | EP1575904B2 (de) |
JP (1) | JP4324558B2 (de) |
KR (1) | KR101032936B1 (de) |
CN (1) | CN1312123C (de) |
AT (1) | ATE484492T1 (de) |
AU (1) | AU2003293871A1 (de) |
DE (2) | DE10260082A1 (de) |
ES (1) | ES2353005T5 (de) |
MX (1) | MXPA05006058A (de) |
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JP2006022098A (ja) * | 2004-07-07 | 2006-01-26 | Bayer Materialscience Ag | 第一級アミンの断熱的ホスゲン化によるポリイソシアネートの製造方法 |
KR101186693B1 (ko) | 2005-04-08 | 2012-09-27 | 헌트스만 인터내셔날, 엘엘씨 | 스파이럴 믹서 노즐, 2개 이상의 유체를 혼합하는 방법 및이소시아네이트 제조 방법 |
EP1890998A2 (de) * | 2005-05-30 | 2008-02-27 | Huntsman International Llc | Verfahren für die zubereitung von polyisocyanaten der diphenylmethan-serie |
EP1890998A4 (de) * | 2005-05-30 | 2011-09-07 | Huntsman Int Llc | Verfahren für die zubereitung von polyisocyanaten der diphenylmethan-serie |
WO2007031444A1 (de) * | 2005-09-13 | 2007-03-22 | Basf Se | Verfahren zur herstellung von isocyanaten |
JP2009507886A (ja) * | 2005-09-13 | 2009-02-26 | ビーエーエスエフ ソシエタス・ヨーロピア | イソシアナートの製造方法 |
US8546605B2 (en) | 2005-09-13 | 2013-10-01 | Basf Aktiengesellschaft | Process for the preparation of isocyanates |
RU2445155C2 (ru) * | 2006-06-26 | 2012-03-20 | Байер Матириальсайенс Аг | Непрерывный способ получения изоцианатов |
EP1873142A1 (de) * | 2006-06-26 | 2008-01-02 | Bayer MaterialScience AG | Verfahren zur kontinuierlichen Herstellung von Isocyanaten |
US7547801B2 (en) | 2006-06-26 | 2009-06-16 | Bayer Materialscience Llc | Process for the continuous preparation of isocyanates |
DE102007061688A1 (de) | 2007-12-19 | 2009-06-25 | Bayer Materialscience Ag | Verfahren und Mischaggregat zur Herstellung von Isocyanaten durch Phosgenierung primärer Amine |
EP2077150A1 (de) | 2007-12-19 | 2009-07-08 | Bayer MaterialScience AG | Verfahren und Mischaggregat zur Herstellung von Isocyanaten durch Phosgenierung primärer Amine |
US8318971B2 (en) | 2008-03-01 | 2012-11-27 | Bayer Materialscience Ag | Process for preparing methylenediphenyl diisocyanates |
DE102008012037A1 (de) | 2008-03-01 | 2009-09-03 | Bayer Materialscience Ag | Verfahren zur Herstellung von Methylen-diphenyl-diisocyanaten |
EP2096102A1 (de) | 2008-03-01 | 2009-09-02 | Bayer MaterialScience AG | Verfahren zur Herstellung von Methylen-diphenyl-diisocyanaten |
WO2011067369A1 (de) | 2009-12-04 | 2011-06-09 | Basf Se | Verfahren zur herstellung von isocyanaten |
US8835673B2 (en) | 2009-12-04 | 2014-09-16 | Basf Se | Process for preparing isocyanates |
WO2012065927A1 (de) | 2010-11-17 | 2012-05-24 | Basf Se | Verfahren zur herstellung von methylendiphenyldiisocyanat |
US8907124B2 (en) | 2010-11-17 | 2014-12-09 | Basf Se | Process for preparing methylenedi(phenyl isocyanate) |
WO2012160072A1 (de) | 2011-05-24 | 2012-11-29 | Basf Se | Verfahren zur herstellung von polyisocyanaten aus biomasse |
US8933262B2 (en) | 2011-05-24 | 2015-01-13 | Basf Se | Process for preparing polyisocyanates from biomass |
WO2021122625A1 (de) | 2019-12-18 | 2021-06-24 | Covestro Deutschland Ag | Verfahren zur herstellung von di- und polyisocyanaten der diphenylmethanreihe |
WO2022048930A1 (en) | 2020-09-01 | 2022-03-10 | Basf Se | Process for producing isocyanates |
Also Published As
Publication number | Publication date |
---|---|
ATE484492T1 (de) | 2010-10-15 |
US7851648B2 (en) | 2010-12-14 |
CN1729168A (zh) | 2006-02-01 |
CN1312123C (zh) | 2007-04-25 |
US20060252960A1 (en) | 2006-11-09 |
AU2003293871A1 (en) | 2004-07-14 |
EP1575904A1 (de) | 2005-09-21 |
EP1575904B1 (de) | 2010-10-13 |
JP2006510692A (ja) | 2006-03-30 |
DE10260082A1 (de) | 2004-07-01 |
EP1575904B2 (de) | 2013-09-04 |
MXPA05006058A (es) | 2005-08-16 |
KR20050089055A (ko) | 2005-09-07 |
ES2353005T5 (es) | 2014-01-09 |
PT1575904E (pt) | 2010-11-09 |
ES2353005T3 (es) | 2011-02-24 |
DE50313194D1 (de) | 2010-11-25 |
JP4324558B2 (ja) | 2009-09-02 |
KR101032936B1 (ko) | 2011-05-06 |
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