WO2000009467A1 - Verfahren zur herstellung von aldehyden und/oder alkoholen oder aminen - Google Patents
Verfahren zur herstellung von aldehyden und/oder alkoholen oder aminen Download PDFInfo
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- WO2000009467A1 WO2000009467A1 PCT/EP1999/005967 EP9905967W WO0009467A1 WO 2000009467 A1 WO2000009467 A1 WO 2000009467A1 EP 9905967 W EP9905967 W EP 9905967W WO 0009467 A1 WO0009467 A1 WO 0009467A1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/60—Preparation of compounds containing amino groups bound to a carbon skeleton by condensation or addition reactions, e.g. Mannich reaction, addition of ammonia or amines to alkenes or to alkynes or addition of compounds containing an active hydrogen atom to Schiff's bases, quinone imines, or aziranes
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J10/00—Chemical processes in general for reacting liquid with gaseous media other than in the presence of solid particles, or apparatus specially adapted therefor
- B01J10/002—Chemical processes in general for reacting liquid with gaseous media other than in the presence of solid particles, or apparatus specially adapted therefor carried out in foam, aerosol or bubbles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/0053—Details of the reactor
- B01J19/006—Baffles
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/24—Stationary reactors without moving elements inside
- B01J19/2455—Stationary reactors without moving elements inside provoking a loop type movement of the reactants
- B01J19/246—Stationary reactors without moving elements inside provoking a loop type movement of the reactants internally, i.e. the mixture circulating inside the vessel such that the upward stream is separated physically from the downward stream(s)
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/26—Nozzle-type reactors, i.e. the distribution of the initial reactants within the reactor is effected by their introduction or injection through nozzles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/49—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
- C07C45/50—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00051—Controlling the temperature
- B01J2219/00074—Controlling the temperature by indirect heating or cooling employing heat exchange fluids
- B01J2219/00087—Controlling the temperature by indirect heating or cooling employing heat exchange fluids with heat exchange elements outside the reactor
- B01J2219/00103—Controlling the temperature by indirect heating or cooling employing heat exchange fluids with heat exchange elements outside the reactor in a heat exchanger separate from the reactor
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00051—Controlling the temperature
- B01J2219/00074—Controlling the temperature by indirect heating or cooling employing heat exchange fluids
- B01J2219/00105—Controlling the temperature by indirect heating or cooling employing heat exchange fluids part or all of the reactants being heated or cooled outside the reactor while recycling
- B01J2219/0011—Controlling the temperature by indirect heating or cooling employing heat exchange fluids part or all of the reactants being heated or cooled outside the reactor while recycling involving reactant liquids
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00162—Controlling or regulating processes controlling the pressure
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00761—Details of the reactor
- B01J2219/00763—Baffles
- B01J2219/00765—Baffles attached to the reactor wall
- B01J2219/00777—Baffles attached to the reactor wall horizontal
Definitions
- the present invention relates to a process for the preparation of aldehydes and / or alcohols or optionally amines by the reaction of olefins with carbon monoxide and hydrogen in the presence or absence of ammonia or a primary or secondary amine in the presence of a catalyst which is homogeneously soluble in the reaction medium and contains at least an element selected from cobalt, rhodium or ruthenium in the presence or absence of a ligand containing phosphorus, arsenic, antimony or nitrogen at elevated temperature and pressure using a nozzle orbital reactor.
- Aldehydes are essentially formed by the hydroformylation of olefins with cobalt carbenyl compounds or rhodium or ruthenium carbonyl complexes which are homogeneously soluble in the reaction medium, generally rhodium carbonyl complexes, which are modified in their reactivity and selectivity with a ligand containing phosphorus, arsenic, antimony or nitrogen. generated.
- Hydroformylation is the reaction of olefins with H 2 / CO mixtures, commonly referred to as synthesis gas, to form aldehydes according to equation (1)
- the area of the hydroformylation reactions also includes the so-called hydrogenating hydroformylation, in which the aldehyde formed in the hydroformylation step is hydrogenated in situ in the hydroformylation reactor from the hydroformylation catalyst to the corresponding alcohol, and the so-called aminating hydroformylation.
- hydrogenating hydroformylation in which the aldehyde formed in the hydroformylation step is hydrogenated in situ in the hydroformylation reactor from the hydroformylation catalyst to the corresponding alcohol
- aminating hydroformylation so-called aminating hydroformylation.
- heterogeneous hydroformylation catalysts can also be used, the use of complexes of these elements which are homogeneously soluble in the hydroformylation medium has become established in industrial use of the hydroformylation reaction.
- Cobalt, rhodium, palladium or ruthenium carbonyl compounds are usually used, and these Compounds are preferred in their reactivity and chemoselectivity by complexing with ligands containing phosphorus, arsenic, antimony or nitrogen.
- the hydroformylation is usually carried out at elevated temperature, the preferred temperature ranges depending on the type of hydroformylation catalyst used.
- a general distinction is made between 3 types of hydroformylation, namely high-pressure hydroformylation, which are carried out at temperatures of generally 140 to 200 ° C. and at a pressure of 100 up to 600 bar, the medium-pressure hydroformylation, which is generally carried out at temperatures from 120 to 180 ° C and in the pressure range from 30 to 100 bar, and the low-pressure hydrofomylation, at which temperatures in general from 60 to 130 ° C and a pressure of 1 up to 30 bar is used.
- catalysts are preferably used for these different hydroformylation processes, specifically in the high-pressure process under the reaction conditions used, carbonyl compounds or hydrocarbonyl compounds not modified with additional organic ligands, preferably cobalt or rhodium, which are among the
- the individual catalysts used in the various hydroformylation processes differ not only in their hydroformylation activity but also in their chemoselectivity, i.e. in their property to preferentially form a certain one of the isomeric hydroformylation products shown in equation (1) and in their property to have other catalytic activities in addition to the hydroformylation activity, which may be more or less desirable depending on the olefin to be hydroformylated and the desired hydroformylation product.
- Such hydrogenation activity of the hydroformylation catalysts is also desirable, for example, in the aminating hydroformylation of olefins, the imine or enamine formed from the resulting aldehyde and a primary or secondary amine present in the reaction medium being hydrogenated in situ to the desired amine.
- Another catalytic side activity of some hydroformylation catalysts is the isomerization of double bonds, for example of olefins with internal double bonds to ⁇ -olefins and vice versa.
- Cobalt carbonyl complexes modified with phosphorus-containing ligands have e.g. not only hydroformylation activity but are also very effective as hydrogenation catalysts, which is why, depending on the CO / H ratio used in the synthesis gas used for the hydroformylation, the aldehydes formed in the hydroformylation of the olefins with such cobalt catalysts are hydrogenated in whole or in part to the corresponding alcohols, so that Depending on the reaction conditions used, alcohols or aldehyde / alcohol mixtures are formed (cf. B. Cornils in J. Falbe, New Syntheses with Carbon Monoxide, Springer Verlag, Berlin [1980] pp. 1-181)
- Reaction liquid in the hydroformylation reactor can be of considerable importance for the economy of the process. Because of its special procedural features, this applies in particular to medium-pressure and low-pressure hydroformylation processes, the improvement of which is the subject of the present invention.
- n-butyl aldehyde and isobutyl aldehyde are formed in the hydroformylation of propene.
- n- and iso-products obtained from the hydroformylation of certain olefins have a different demand for the respective n- and iso-products obtained from the hydroformylation of certain olefins. Efforts are therefore made to generate these isomeric aldehydes in a specific n / iso ratio which corresponds to the need for the individual isomers.
- the n / iso ratio can be influenced to a certain extent by setting certain reaction parameters in the hydroformylation reactor.
- n / iso ratio of the aldehyde product produced in the hydroformylation with Rh / TPP catalysts is significantly influenced by the ratio of the carbon monoxide and triphenylphosphine concentration [CO] / [TPP] in the reaction liquid.
- CO carbon monoxide
- RZA Space-time yield
- the hydroformylation reactor Since the chemical composition of the reaction liquid changes in the technical operation of the hydroformylation process due to the formation of the hydroformylation products and by-products, such as high boilers of different chemical compositions, and the absorption capacity of such reaction mixtures for the dispersed bubbles of the reaction gas is not known at every operating point, it can in extreme cases, the hydroformylation reactor overflows due to an excessively high volumetric total part in the reaction liquid, to avoid which the hydroformylation reactor is engineered with a larger volume than would be necessary for capacity reasons.
- EP-A 188 246, EP-A 423 769 and WO 95/08525 propose the use of stirrers or gassing stirrers or the use of the reaction gas streams introduced into the reaction liquid to mix the reaction liquid.
- gas distributors are used, the size, number and position of which in the reactor depend on the size of the reactor.
- the heat of reaction is removed using internal, external or external heat exchangers.
- hydroformylation creator is strongly exothermic and its selectivity, as explained above, is sensitive to concentration gradients and temperature inhomogeneities in the liquid reaction medium, thorough mixing of the reaction liquid must be ensured, otherwise there is a risk that the stable operating range of the reactor, for example due to local overheating is left, with the result of loss of yield and selectivity.
- bubble columns are used to carry out the hydroformylation reaction in industry.
- the reaction gases are introduced at the lower end of the bubble column through a gas distributor, which ensures that the reaction gases are dispersed in the reaction liquid in order to increase the mass transfer area.
- the fine gas bubbles rise according to their lower density in the reaction liquid, causing the reaction liquid to is mixed.
- some of the gases from the gas bubbles diffuse through the gas / liquid interface into the reaction liquid, where they react in dissolved form in the hydroformylation reaction.
- the bubble column is operated by a correspondingly adjusted supply of the reaction gases at a relatively low volumetric gas fraction e G , the length of the liquid column in the bubble column leads to the formation of [CO] concentration gradients and temperature inhomogeneities with the described disadvantageous consequences on yield and Selectivity.
- a high volumetric gas fraction required for the ideal mixing of the reaction liquid a large part of the available reaction space is uselessly occupied by the gas bubbles, as a result of which the RZA drops.
- EP-A 254 180 to introduce part of the reaction gases into the reaction liquid via different feeds at different heights of the reactor designed as a bubble column. This measure reduces the [CO] gradient from usually 10% to 2%.
- DE-A 2810644 relates to the use of a flooded reactor, ie a reactor whose entire volume is filled by the reaction liquid, for hydroformylation reactions in which the liquid and gaseous reactants are fed into the lower part of the reactor and inside a tubular one in the reactor Guide element, the lower and upper ends of which are located at a distance from the reactor base and the reactor cap, respectively, are guided into the upper part of the reactor.
- the upward flow of the reaction liquid is reversed so that it flows downward in the space between the wall of the guide member and the reactor wall, where it is redirected into a flow flowing upward inside the guide member when it hits the reactor bottom or suitable deflection devices.
- Part of the reaction mixture is continuously removed for product isolation at a removal point in the lower part of the reactor, which is attached in such a way that practically only reaction liquid is removed from the downward flowing flow.
- the volumes of the reactor rooms with upward or downward flow are approximately the same size.
- the reaction rate in the high-pressure hydroformylation catalyzed with cobalt carbonyls is many times lower than in the low-pressure hydroformylation catalyzed with rhodium carbonyl ligand complexes.
- the aim of the application of the reactor construction described in DE-A 2810644 is to increase the residence time of the reaction liquid by increasing the distance traveled by the reaction liquid in the reactor in order to achieve a higher olefin conversion. The avoidance of gradient formation is not addressed in DE-A 2810644.
- the rate of the hydroformylation reaction is kinetically controlled in a wide range of parameters, ie the rate of mass transfer from the gas phase to the liquid phase does not have a limiting effect on the rate of reaction of the hydroformylation under the hydroformylation conditions customarily used .
- the RZA increases as the volumetric gas fraction e G decreases.
- the volumetric gas fraction e G cannot be reduced arbitrarily, since the limit is exceeded at some point where the speed of the substance - transition from the gas phase to the liquid phase becomes limiting for the reaction rate of the hydroformylation reaction.
- the boundary between kinetic and mass transfer-influenced control of the reaction rate of the hydroformylation reaction is fluid. It is complex in terms of the type of mechanical power input into the reaction liquid, the specific phase interface between gas and reaction liquid, expressed in m 2 / m 3 , and the physical properties shadow depending on the reaction system. An exact advance calculation has not yet been successful.
- the reaction according to FIG. 1 is carried out in a reactor 1, comprising the reactor body 2 and at least one circulation line 3, as well as supply and discharge devices for the reactants and the reaction discharge, the reactor body 2, preferably being made from a calming space below the baffle plate 7 continuously removes a portion of the reaction liquid via at least one circulation line 3 and wherein a jet is generated with at least one nozzle 5 located in the upper part of the reactor body 2 and generates a downward flow in at least one guide element 6 mounted in the reactor, the impingement device in the form of a baffle plate 7, after impinging on at least one guide element or guide elements 6, is deflected into a flow flowing upwards in the space 8 between the reactor body 2 and the relevant guide element 6, in the reactor body 2 at least one guide member 6 is attached so that
- Reaction liquid and at least one nozzle 5 assigned to this guide element 6 is located in an approximately concentric position with respect to the cross-sectional area of this guide element 6,
- the reactor 1 which can be used in the process according to the invention generally comprises a pressure-stable reactor body 2 and at least one circulation line 3.
- the cross-sectional shape of the reactor body 2 is in principle not critical for the feasibility of the process according to the invention and can be triangular, square, square, rectangular, diamond-shaped, trapezoidal, be pentagonal, hexagonal, polygonal, elliptical or circular, preferably it is circular.
- part of the reaction liquid is continuously removed from the reactor body 2, which has been filled with the reaction liquid up to the level of the liquid level 9, during operation, via the circulation line 3, and at least one nozzle fitted in the upper part of the reactor 5 supplied, for which purpose a pump 4 integrated in the circulation line 3 can advantageously be used.
- one or more heat exchangers 12 for heating and / or cooling the reaction liquid can also be installed in the circulation line 3.
- the reaction liquid can be removed at any height of the reactor body 2; the reaction liquid is preferably removed from a flow-reduced zone at the lower end of the reactor body 2.
- a pump 4 which is able to pump gas / liquid mixtures, for example a side channel pump.
- the content of dispersed gas bubbles in the withdrawn reaction liquid generally depends on the location of the withdrawal, it is generally much higher in the areas of the reactor with high flow than in the flow-reduced zone at the lower end of the reactor, i.e. below the baffle where it can be practically neglected.
- the nozzle 5 is mounted in the upper part of the reactor body, preferably in the head space 10 filled with reaction gases, so that its nozzle tip is in the operating state in the region or below the liquid level but above a guide member 6 assigned to the nozzle 5.
- any nozzle construction suitable for generating a liquid jet can be used as the nozzle 5, in a particularly preferred embodiment.
- the nozzle 5 is designed as a two-substance nozzle with which the reaction gas is sucked in by the liquid jet generated in the nozzle, mixed into it and dispersed with it in the reaction liquid in the form of fine gas bubbles.
- the nozzle 5 is assigned a guide element 6 which is open at the top and bottom and which has the same cross-sectional shape of the reactor body but can also be different from the latter.
- the guide member 6 preferably has the same cross-sectional shape as the reactor body 2, is advantageously circular, and in the case of the simplest embodiment of the method according to the invention is preferably attached in the central position in the interior of the reactor body via conventional fastening devices.
- the shape of the guide element 6 corresponds to that of an open tube, which is why it is also referred to below as a plug-in tube.
- the guide element 6 is advantageously arranged in the reactor body with respect to the nozzle 5 such that the nozzle tip 11 is located in the center, that is to say in an approximately concentric position, preferably in an exactly concentric position, with respect to the inner cross-sectional area of the guide element 6.
- the upper end of the insertion tube 6 is advantageously below the liquid level 9 of the reaction liquid at a distance a from the nozzle tip 11.
- the distance a can be varied depending on the energy input of the liquid jet generated by the nozzle 5, in general it is 0.1 to 0.8 times, preferably 0.2 to 0.4 times the inside diameter of the reactor.
- the lower end of the insertion tube 6 is generally at a distance b above the reactor base 13 or, in the case of the preferred use of a deflection device 7, which can be configured, for example, as a baffle plate, at a distance b from this deflection device 7.
- the size of the distance b can be in wide ranges can be varied, and should only be large enough so that the liquid flow can leave the insertion tube 7 unhindered.
- the distance b is 0.15 to 1.2 times, preferably 0.3 to 0.6 times the inner diameter of the reactor.
- the deflection device 7 is expediently installed at a certain distance from the reactor base 13, this distance in principle being arbitrary.
- the space between the deflection device 7 and the reactor bottom 13 is also filled with reaction liquid and is with the reaction liquid above the deflection device 7, for example above a passage between the deflection device 7 and the wall of the reactor body 2 or via passages in the deflection. Device 7 in intimate contact. If, according to a preferred embodiment of the process according to the invention, part of the reaction liquid is removed through the circulation line 3 from a flow-reduced zone in the lower part of the reactor body 2, this is advantageously done via a removal point which is located in the space between the deflection device 7 and the reactor base 13.
- the insertion tube 6 is dimensioned such that the ratio of its inner cross sectional area to the total inner cross sectional area of the reactor body 2, which is calculated from its inner diameter D, is generally 0.03 to 0.6, preferably 0.06 to 0.4 and is particularly preferably 0.1 to 0.36.
- their inside cross-sectional area is designed such that the ratio of the sum of the inside cross-sectional areas of these insertion tubes 6 to the total inside cross-sectional area of the reactor body 2 lies in the aforementioned ranges.
- the ratio of the length L of the insertion tube 6 to its inside diameter d is generally 3 to 40, preferably 4 to 20 and particularly preferably 6 to 12.
- the gaseous reactants i.e. the synthesis gas and, if appropriate, gaseous olefins, and, if desired, inert gases mixed with these gaseous reactants, as well as the liquid reactants, i.e. the olefin, optionally in liquefied form and catalyst solution, and, if desired, solvents for the hydroformylation reaction, can be reacted to the reactor 1 in principle be fed to any point of the reactor 1.
- the gaseous reactants are preferably introduced below the baffle plate 7 (stream 14).
- gaseous inflows can also be introduced, for example, into the head space 10 and at various points along the reactor, as is indicated by the flows 15 and 16. This becomes particularly important when the gaseous streams are stripping gas. It is also conceivable to introduce a gas stream, in particular if the gases involved in the reaction, via a two-component nozzle. The same applies to liquid inflows. Preferred places here are stream 20 or addition via a two-component nozzle (stream 18).
- the liquid phase is preferably taken from the reactor as a partial stream (stream 21) from the pump circuit (3). Other places are also conceivable.
- the gaseous phase is preferably withdrawn from the head space (10) via stream (11) from the reactor. Other possibilities, for example below the baffle plate (17) ' , are also conceivable.
- the fill level H remains constant.
- the volume of the drained liquid is only replaced by gas.
- the gas is sucked out of the head space via the nozzle and carried away by the downward flow.
- the gas that is conveyed downwards in the insertion tube rises again in the gap space.
- the nozzle (5) draws gas from the headspace until the liquid level touches the nozzle mouth.
- the reactor is thus able to internally pump gas in the circuit.
- the baffle plate (17) suppresses the entrainment of gas bubbles in the external pump circuit.
- the gas can be completely displaced from the circulating flow.
- regulation of the gas content is possible.
- the gas content in the external space (8) which is accessible via the pressure measuring points P / 1 and P / 2, can be used for the control.
- a prerequisite for the formation of the two-phase circulating flow is that the flow speed in the plug-in tube is greater than the rate of rise of the dispersed gas phase.
- the internally circulated liquid flow is many times larger than the volume flow of the jet.
- the internally promoted circulating gas flow can be a multiple of the gas flows supplied from the outside. Concentration and temperature gradients in the liquid phase are reduced very strongly.
- the reactor can thus be in the entire volume
- the reactor to be used according to the invention offers a number of advantages which are particularly important for hydroformylation, such as:
- Adjustable and controllable gas content - high space-time yield large internal circulation flows and therefore flat gradients no external gas circulation (circulating gas compressor) decoupling of gas content and feed gas flows high mass transfer rate between liquid and gas high power inputs possible simple cooling via external circuit high CO conversion
- reaction conditions of the hydroformylation or the aminating hydroformylation are well known from the specialist literature. More specifically, B. Cornils in J. Falbe, New Syntheses with Carbon Monoxide, Springer Verlag, Berlin [1980] pp. 1-181. As a rule, the hydroformylation or aminating hydroformylation to be carried out according to the invention is carried out as in M. Beller, B. Cornils, CD. Frohning, CW Kohlpainter, J. Mol. Catal. A, 104 (1995) 17-85.
- hydroformylatable olefins are suitable as starting materials, in particular aliphatic olefins having 2 to 20 C atoms, preferably ⁇ -olefins or internal linear olefins having 2 or 4 to 20 C atoms.
- FIG. 2 A continuous mini-plant, which is shown schematically in FIG. 2 and is explained below, was used for the experiments in the following example. Of course, plant details that are not required to illustrate the method according to the invention were not included in FIG. 2 for reasons of clarity.
- the plant could be operated either with a mechanically stirred autoclave (R) as the reactor or with a reactor (G) to be used according to the invention.
- the autoclave behaves as in an ideally mixed stirred tank reactor.
- olefin or CO / H 2 mixture is fed into the calysator + high boiler recycle stream and alternatively via line (3) either via line (5) into the gas circulation reactor (G) to be used according to the invention or into the stirred tank reactor (R) initiated.
- the hydroformylation output from the reactor was passed via line (6/9 or (8/9) after depressurization and separation of the liquid phase from excess synthesis gas in the pressure cutter (A) via line 10 of a distillative workup (consisting of flash (F) and Sambay evaporator ( D))
- the bottom from the distillative separation was returned to the hydroformylation stage via line 15.
- the exhaust gas is removed via line 11, the unreacted olefins via line 12 and the aldehydes formed via line 14.
- a continuous experiment was carried out in a gas circulation reactor (G) to be used according to the invention with a total volume of 5 4.35 l.
- the gas circulation reactor accounts for 3.6 l, the pump circulation 0.75 1. Due to the large circulation volume, the pump circulation must be counted among the active reactor volumes.
- the catalyst-containing sump was returned to the reactor via line 15.
- the rhodium concentration in the reactor was approximately 120 ppm.
- the ligand / rhodium ratio was 120: 1 (mol / mol).
- the high boilers formed under the reaction conditions were used as solvents
- a circulation rate of 145 kg / h was pumped through line (7) through a 1.8 mm diameter nozzle into the
- the gas content in the reactor was set to 10%, which corresponds to a gas volume of 0.345 l, and was kept constant.
- the desired selectivity to the linear isomer was achieved by varying the CO / H ratio in the fresh gas.
- the load was 450 g / (h propylene (99.3%, remainder propane). After starting up the plant, a propylene conversion of 84% was achieved with a selectivity to aldehydes of 95% with an n content of 87% was based on the total volume
- a circulation rate of 145 kg / h was conveyed into the reactor through line (7) using a pump.
- the gas content in the reactor was set at 2% and kept constant.
- the Gas volume was thus only about 0.07 l.
- the gas content based on the total volume was thus about 6% smaller than in example 1.
- the desired selectivity to the linear isomer was achieved by varying the CO / H 2 ratio in the fresh gas.
- the load was 450 g / h of propylene (99.3%, remainder propane). After starting up the plant, the same propylene conversion as in Example 1 was measured within the scope of the measurement accuracy and the same selectivity to aldehydes with 95%. Despite the lower gas content, the CO partial pressure did not change and the n portion of 87% was reached again.
- a continuous test was carried out in a 2.5-1 stroke autoclave with internal cooling (available liquid volume 1.7 l). After removal of excess olefin in the flash and removal of the reaction product on a Sambay evaporator, the catalyst-containing bottoms were returned to the reactor.
- the rhodium concentration in the reactor was approximately 100 ppm.
- the ligand / rhodium ratio was 120: 1 (mol / mol).
- the high boilers formed under the reaction conditions were used as solvents. CO / H 2 in a ratio of 1: 1 was used, the pressure (20 bar) and the temperature (105 ° C) were kept constant.
- the load was 250 g / h propene (99.3%, remainder propane). After starting up the plant, a propylene conversion of 80% was achieved with a selectivity to aldehydes of 92% with an n content of 88%.
- the RZA was only 125 g (lh) due to the large, uncontrollable gas content.
Abstract
Description
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Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT99942870T ATE234802T1 (de) | 1998-08-14 | 1999-08-13 | Verfahren zur herstellung von aldehyden und/oder alkoholen oder aminen |
JP2000564922A JP2002522518A (ja) | 1998-08-14 | 1999-08-13 | アルデヒドおよび/またはアルコールまたはアミンの製造法 |
DE59904660T DE59904660D1 (de) | 1998-08-14 | 1999-08-13 | Verfahren zur herstellung von aldehyden und/oder alkoholen oder aminen |
US09/762,425 US6642420B1 (en) | 1998-08-14 | 1999-08-13 | Method for producing aldehydes and/or alcohols or amines |
EP99942870A EP1114017B1 (de) | 1998-08-14 | 1999-08-13 | Verfahren zur herstellung von aldehyden und/oder alkoholen oder aminen |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19836807.0 | 1998-08-14 | ||
DE19836807A DE19836807A1 (de) | 1998-08-14 | 1998-08-14 | Verfahren zur Herstellung von Aldehyden und/oder Alkoholen oder Aminen |
Publications (1)
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EP (1) | EP1114017B1 (de) |
JP (1) | JP2002522518A (de) |
KR (1) | KR100580423B1 (de) |
CN (1) | CN1165506C (de) |
AT (1) | ATE234802T1 (de) |
DE (2) | DE19836807A1 (de) |
ES (1) | ES2194500T3 (de) |
MY (1) | MY124357A (de) |
TW (1) | TW541298B (de) |
WO (1) | WO2000009467A1 (de) |
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US7321068B2 (en) | 2003-12-09 | 2008-01-22 | Basf Aktiengesellschaft | Method for producing tricyclodecandialdehyde |
KR100960763B1 (ko) * | 2002-01-17 | 2010-06-01 | 바스프 에스이 | 탄소수 2 내지 6의 올레핀의 히드로포르밀화 방법 |
US10315975B2 (en) | 2015-07-10 | 2019-06-11 | Basf Se | Method for the hydroformylation of 2-substituted butadienes and the production of secondary products thereof, especially ambrox |
US10647651B2 (en) | 2015-10-12 | 2020-05-12 | Basf Se | Hydroformylation process for producing 1,6-disubstituted hexane derivatives |
US10941092B2 (en) | 2017-06-13 | 2021-03-09 | Basf Se | Hydroformylation process for producing 1,6-hexanediol derivatives |
FR3117891A1 (fr) * | 2020-12-23 | 2022-06-24 | IFP Energies Nouvelles | Reacteur gaz/liquide d’oligomerisation comprenant une conduite centrale |
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- 1999-08-13 WO PCT/EP1999/005967 patent/WO2000009467A1/de active IP Right Grant
- 1999-08-13 DE DE59904660T patent/DE59904660D1/de not_active Expired - Lifetime
- 1999-08-13 AT AT99942870T patent/ATE234802T1/de not_active IP Right Cessation
- 1999-08-13 ES ES99942870T patent/ES2194500T3/es not_active Expired - Lifetime
- 1999-08-13 EP EP99942870A patent/EP1114017B1/de not_active Expired - Lifetime
- 1999-08-13 JP JP2000564922A patent/JP2002522518A/ja active Pending
- 1999-08-13 CN CNB998096792A patent/CN1165506C/zh not_active Expired - Lifetime
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100960763B1 (ko) * | 2002-01-17 | 2010-06-01 | 바스프 에스이 | 탄소수 2 내지 6의 올레핀의 히드로포르밀화 방법 |
US7196230B2 (en) | 2002-03-11 | 2007-03-27 | Union Carbide Chemicals & Plastics Technology Corporation | Phosoxophite ligands and use thereof in carbonylation processes |
US7294729B2 (en) | 2002-10-15 | 2007-11-13 | Union Carbide Chemicals & Plastics Technology Corporation | Bis-chelating ligand and use thereof in carbonylation processes |
US7321068B2 (en) | 2003-12-09 | 2008-01-22 | Basf Aktiengesellschaft | Method for producing tricyclodecandialdehyde |
US10315975B2 (en) | 2015-07-10 | 2019-06-11 | Basf Se | Method for the hydroformylation of 2-substituted butadienes and the production of secondary products thereof, especially ambrox |
US10647651B2 (en) | 2015-10-12 | 2020-05-12 | Basf Se | Hydroformylation process for producing 1,6-disubstituted hexane derivatives |
US10941092B2 (en) | 2017-06-13 | 2021-03-09 | Basf Se | Hydroformylation process for producing 1,6-hexanediol derivatives |
FR3117891A1 (fr) * | 2020-12-23 | 2022-06-24 | IFP Energies Nouvelles | Reacteur gaz/liquide d’oligomerisation comprenant une conduite centrale |
WO2022136012A1 (fr) * | 2020-12-23 | 2022-06-30 | IFP Energies Nouvelles | Procede d'oligomerisation dans un reacteur gaz/liquide comprenant une conduite centrale |
Also Published As
Publication number | Publication date |
---|---|
EP1114017A1 (de) | 2001-07-11 |
ATE234802T1 (de) | 2003-04-15 |
JP2002522518A (ja) | 2002-07-23 |
KR100580423B1 (ko) | 2006-05-16 |
CN1312785A (zh) | 2001-09-12 |
DE19836807A1 (de) | 2000-02-17 |
KR20010072453A (ko) | 2001-07-31 |
ES2194500T3 (es) | 2003-11-16 |
EP1114017B1 (de) | 2003-03-19 |
DE59904660D1 (de) | 2003-04-24 |
CN1165506C (zh) | 2004-09-08 |
US6642420B1 (en) | 2003-11-04 |
TW541298B (en) | 2003-07-11 |
MY124357A (en) | 2006-06-30 |
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