CA2863836A1 - Process for preparing higher molecular weight polyisobutylene - Google Patents
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Abstract
The invention relates to the production of isobutylene homopolymers having a weight-average molecular weight of 75,000 to 10,000,000 by means of the polymerization of isobutylene by (a) performing the polymerization at -80°C to -190°C, (b) using optionally halogenated C1 to C5 hydrocarbons as an inert solvent, (c) using a Lewis acid complex as a polymerization catalyst, and (d) performing the polymerization in the presence of at least one reaction accelerator in the form of an ethylenically saturated hydrocarbon compound, which contains an oxygen atom and no proton that can be emitted, and performing the polymerization in the presence of at least one chain length regulator, which contains a tertiary olefinic carbon atom.
Description
PROCESS FOR PREPARING HIGHER MOLECULAR WEIGHT POLYISOBUTYLENE
Description The present invention relates to an improved process for preparing isobutene homopolymers having a weight-average molecular weight of 75 000 to 10 000 000 by polymerization of isobutene in the liquid phase in an inert solvent in the presence of a polymerization catalyst based on Lewis acids.
Efficient preparation processes which satisfy the specification for higher molecular weight polyisobutenes generally entail very low polymerization temperatures. A
typical process for preparing higher molecular weight polyisobutenes is called the "BASF belt process", in which liquid isobutene together with boron trifluoride as a polymerization catalyst and a high excess of liquid ethene are passed onto a continuous steel belt of width from 50 to 60 cm, which is configured in a trough shape by suitable guiding and is present in a gas-tight cylindrical casing. Constant evaporation of the ethene at standard pressure sets a temperature of -104 C. This fully removes the heat of polymerization. The evaporated ethene is collected, purified and recycled. The resulting polyisobutenes are freed of ethene which still adheres and residual monomers by degassing. The polymerization of this type leads to virtually full isobutene conversion.
In the BASF belt process, the polymerization temperature can be controlled easily and reliably owing to evaporative cooling, i.e. as a result of formation of large vapor passages.
However, a disadvantage of the BASF belt process is that, owing to lack of movement of the reaction material on the belt, inadequate mixing of the reaction material and hence no product surface renewal takes place, which can have a disadvantageous effect on the product properties. This leads, for example, to inhomogeneous distribution of the ethene used for evaporative cooling and associated local overheating of the reaction mixture as soon as the ethene has vaporized. In addition, there may be explosive boiling of the reaction mixture when overheated regions and ethene-rich cold regions come into contact with one another, which then leads to soiling of the reactor wall as a result of entrainment of polymerizing reaction mixture. Another disadvantage is that the inhomogeneous temperature distribution causes unwanted broadening of the molecular weight distribution of the polymer, which is associated with unfavorable product properties. A further disadvantage of the BASF
belt process is that the steel belt is subject to wear and thus causes high maintenance costs.
A further disadvantage of the BASF belt process is that the reactor walls and the product
Description The present invention relates to an improved process for preparing isobutene homopolymers having a weight-average molecular weight of 75 000 to 10 000 000 by polymerization of isobutene in the liquid phase in an inert solvent in the presence of a polymerization catalyst based on Lewis acids.
Efficient preparation processes which satisfy the specification for higher molecular weight polyisobutenes generally entail very low polymerization temperatures. A
typical process for preparing higher molecular weight polyisobutenes is called the "BASF belt process", in which liquid isobutene together with boron trifluoride as a polymerization catalyst and a high excess of liquid ethene are passed onto a continuous steel belt of width from 50 to 60 cm, which is configured in a trough shape by suitable guiding and is present in a gas-tight cylindrical casing. Constant evaporation of the ethene at standard pressure sets a temperature of -104 C. This fully removes the heat of polymerization. The evaporated ethene is collected, purified and recycled. The resulting polyisobutenes are freed of ethene which still adheres and residual monomers by degassing. The polymerization of this type leads to virtually full isobutene conversion.
In the BASF belt process, the polymerization temperature can be controlled easily and reliably owing to evaporative cooling, i.e. as a result of formation of large vapor passages.
However, a disadvantage of the BASF belt process is that, owing to lack of movement of the reaction material on the belt, inadequate mixing of the reaction material and hence no product surface renewal takes place, which can have a disadvantageous effect on the product properties. This leads, for example, to inhomogeneous distribution of the ethene used for evaporative cooling and associated local overheating of the reaction mixture as soon as the ethene has vaporized. In addition, there may be explosive boiling of the reaction mixture when overheated regions and ethene-rich cold regions come into contact with one another, which then leads to soiling of the reactor wall as a result of entrainment of polymerizing reaction mixture. Another disadvantage is that the inhomogeneous temperature distribution causes unwanted broadening of the molecular weight distribution of the polymer, which is associated with unfavorable product properties. A further disadvantage of the BASF
belt process is that the steel belt is subject to wear and thus causes high maintenance costs.
A further disadvantage of the BASF belt process is that the reactor walls and the product
2 intake in the downstream workup section (usually an extruder) are not cooled;
since polyisobutylene is highly tacky above its glass transition temperature, this leads to significant coverage of the reactor walls with sticky polymer, which necessitates an increased level of cleaning. A further disadvantage of the BASF belt process is that boron trifluoride present in the recycled ethene stream is highly corrosive at relatively high temperatures, which causes a high level of maintenance in the ethene workup circuit.
A further customary process for preparing higher molecular weight polyisobutenes is the "Exxon slurry process", in which the polymerization is performed at -80 to -85 C in a stirred tank equipped with a cooling jacket which is charged with liquid ethene. The catalyst system used is anhydrous aluminum chloride in methyl chloride. Owing to the very vigorous stirring, the polymer is obtained as a slurry consisting of small droplets which flows via an intermediate vessel into a degassing vessel. Here, the slurry is treated with steam and hot water so that the volatile constituents (essentially unconverted isobutene and methyl chloride) can be removed and sent to reprocessing. The remaining liquid slurry of the polymer particles is worked up by removing catalyst residues, solvent residues and isobutene residues.
In the Exxon slurry process, although intensive mixing and product surface renewal takes place, the polymerization temperature is difficult to control solely by the jacket cooling. Since the polymer cannot completely be prevented from adhering to the reactor and apparatus walls, reactor and apparatus have to be cleaned from time to time.
The BASF belt process and the Exxon slurry process are described in detail in Ullmann's Encyclopedia of Industrial Chemistry, 5th edition, Vol. A21, pp. 555-561, under "polyisobutylenes".
It was an object of the present invention to provide an easily performable, efficient and economically viable process for preparing higher molecular weight isobutene homopolymers, which, with regard to the product parameters to be established, such as molecular weight, polydispersity and residual monomer content, allows reliable control of the polymerization and affords an easily purifiable and efficiently manageable product, in particular one which does not stick prior to workup. Due to the comparatively intense mixing of the reaction mixture, the polymerization should be performed in a customary closed reactor and in the disperse phase in an immiscible fluid or mixed homogeneously in a miscible fluid, i.e. in a suitable solvent or diluent.
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since polyisobutylene is highly tacky above its glass transition temperature, this leads to significant coverage of the reactor walls with sticky polymer, which necessitates an increased level of cleaning. A further disadvantage of the BASF belt process is that boron trifluoride present in the recycled ethene stream is highly corrosive at relatively high temperatures, which causes a high level of maintenance in the ethene workup circuit.
A further customary process for preparing higher molecular weight polyisobutenes is the "Exxon slurry process", in which the polymerization is performed at -80 to -85 C in a stirred tank equipped with a cooling jacket which is charged with liquid ethene. The catalyst system used is anhydrous aluminum chloride in methyl chloride. Owing to the very vigorous stirring, the polymer is obtained as a slurry consisting of small droplets which flows via an intermediate vessel into a degassing vessel. Here, the slurry is treated with steam and hot water so that the volatile constituents (essentially unconverted isobutene and methyl chloride) can be removed and sent to reprocessing. The remaining liquid slurry of the polymer particles is worked up by removing catalyst residues, solvent residues and isobutene residues.
In the Exxon slurry process, although intensive mixing and product surface renewal takes place, the polymerization temperature is difficult to control solely by the jacket cooling. Since the polymer cannot completely be prevented from adhering to the reactor and apparatus walls, reactor and apparatus have to be cleaned from time to time.
The BASF belt process and the Exxon slurry process are described in detail in Ullmann's Encyclopedia of Industrial Chemistry, 5th edition, Vol. A21, pp. 555-561, under "polyisobutylenes".
It was an object of the present invention to provide an easily performable, efficient and economically viable process for preparing higher molecular weight isobutene homopolymers, which, with regard to the product parameters to be established, such as molecular weight, polydispersity and residual monomer content, allows reliable control of the polymerization and affords an easily purifiable and efficiently manageable product, in particular one which does not stick prior to workup. Due to the comparatively intense mixing of the reaction mixture, the polymerization should be performed in a customary closed reactor and in the disperse phase in an immiscible fluid or mixed homogeneously in a miscible fluid, i.e. in a suitable solvent or diluent.
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3 The polymerization of isobutene to give higher molecular weight isobutene homopolymers in customary closed reactors in solvents or diluents is also known from other documents as well as the Exxon slurry process described. For instance, DE-A 2 061 289 discloses an isobutene polymerization process in which isobutene is polymerized between 0 C and -160 C in an In the monograph "Polymerization and Polycondensation Processes, Advances in Chemistry The literature article "Fundamental Studies on Cationic Polymerization IV ¨
Homo- and Co-polymerizations with Various Catalysts" by J. P. Kennedy and R. G. Squires in Polymer 6, catalysis in alkyl chloride solvents at -30 C to -146 C in the presence of isoprene to give higher molecular weight polyisobutene. Reaction accelerators are not used.
The object of the present invention is achieved by a process for preparing isobutene (b) using, as an inert solvent, one or more Ci to C8 hydrocarbons or one or more halogenated Ci to 08 hydrocarbons or a mixture thereof and
Homo- and Co-polymerizations with Various Catalysts" by J. P. Kennedy and R. G. Squires in Polymer 6, catalysis in alkyl chloride solvents at -30 C to -146 C in the presence of isoprene to give higher molecular weight polyisobutene. Reaction accelerators are not used.
The object of the present invention is achieved by a process for preparing isobutene (b) using, as an inert solvent, one or more Ci to C8 hydrocarbons or one or more halogenated Ci to 08 hydrocarbons or a mixture thereof and
4 (c) using, as a polymerization catalyst, a Lewis acid complex based on boron trifluorid, on iron halides, on aluminum trihalides or on aluminum alkyl halides or a Lewis acid in combination with organic sulfonic acids as initiators, and additionally (d) performing the polymerization in the presence of at least one reaction accelerator in the form of an ethylenically saturated hydrocarbon compound comprising at least one oxygen atom and no abstractable proton, and/or (e) performing the polymerization in the presence of at least one chain length regulator comprising at least one tertiary olefinic carbon atom.
In a preferred embodiment, measures (d) and (e) are both performed.
In the context of the present invention, isobutene homopolymers are understood to mean those polymers which, based on the polymer, are composed of isobutene to an extent of at least 98 mol%, preferably to an extent of at least 99 mol%.
For the use of isobutene, or of the isobutenic monomer mixture as the monomer to be polymerized, suitable isobutene sources are, more particularly, pure isobutene which generally comprises at most 0.5% by volume of residual impurities such as 1-butene, 2-butenes, butane, water and/or Ci- to 04- alkanols. However, it is also possible in principle to use isobutenic technical C4 hydrocarbon streams, for example, C4 raffinates, C4 cuts from isobutane dehydrogenation, 04 cuts from steamcrackers and from FCC crackers (fluid catalyzed cracking), provided that they have been substantially freed of 1,3-butadiene present therein. Suitable technical 04 hydrocarbon streams comprise generally less than 500 ppm, preferably less than 200 ppm, of butadiene. The isobutene from such technical C4 hydrocarbon streams is polymerized here substantially selectively to the desired isobutene homopolymer without incorporation of significant amounts of other 04 monomers into the polymer chain. Typically, the isobutene concentration in the technical 04 hydrocarbon streams mentioned is in the range from 40 to 60% by weight. However, the process according to the invention can in principle also be operated with isobutenic C4 hydrocarbon streams which comprise less isobutene, for example, only 10 to 20% by weight.
The isobutenic monomer mixture may comprise small amounts of contaminants such as water, carboxylic acids or mineral acids without any critical yield or selectivity losses. It is appropriate to the purpose to avoid accumulation of these impurities by removing such , =
harmful substances from the isobutenic monomer mixture, for example, by adsorption on solid adsorbents such as activated carbon, molecular sieves or ion exchangers.
The Lewis acid complexes which are to be used as a polymerization catalyst according to
In a preferred embodiment, measures (d) and (e) are both performed.
In the context of the present invention, isobutene homopolymers are understood to mean those polymers which, based on the polymer, are composed of isobutene to an extent of at least 98 mol%, preferably to an extent of at least 99 mol%.
For the use of isobutene, or of the isobutenic monomer mixture as the monomer to be polymerized, suitable isobutene sources are, more particularly, pure isobutene which generally comprises at most 0.5% by volume of residual impurities such as 1-butene, 2-butenes, butane, water and/or Ci- to 04- alkanols. However, it is also possible in principle to use isobutenic technical C4 hydrocarbon streams, for example, C4 raffinates, C4 cuts from isobutane dehydrogenation, 04 cuts from steamcrackers and from FCC crackers (fluid catalyzed cracking), provided that they have been substantially freed of 1,3-butadiene present therein. Suitable technical 04 hydrocarbon streams comprise generally less than 500 ppm, preferably less than 200 ppm, of butadiene. The isobutene from such technical C4 hydrocarbon streams is polymerized here substantially selectively to the desired isobutene homopolymer without incorporation of significant amounts of other 04 monomers into the polymer chain. Typically, the isobutene concentration in the technical 04 hydrocarbon streams mentioned is in the range from 40 to 60% by weight. However, the process according to the invention can in principle also be operated with isobutenic C4 hydrocarbon streams which comprise less isobutene, for example, only 10 to 20% by weight.
The isobutenic monomer mixture may comprise small amounts of contaminants such as water, carboxylic acids or mineral acids without any critical yield or selectivity losses. It is appropriate to the purpose to avoid accumulation of these impurities by removing such , =
harmful substances from the isobutenic monomer mixture, for example, by adsorption on solid adsorbents such as activated carbon, molecular sieves or ion exchangers.
The Lewis acid complexes which are to be used as a polymerization catalyst according to
5 measure (c) and are based on iron halides, on aluminum trihalides or on aluminum alkyl halides, and Lewis acids which are to be used as a polymerization catalyst in combination with organic sulfonic acids as initiators, are described in detail in WO
2012/072643 A2, explicit reference being made here thereto. The iron halide, aluminum trihalide and aluminum alkyl halide complexes mentioned comprise, as well as the Lewis acid, a donor in the form of an organic compound having at least one ether function or a carboxylic ester function. This combination of Lewis acids, especially of boron trifluoride, iron halides, aluminum trihalides or aluminum alkyl halides, with organic sulfonic acids as initiators comprise at least one organic sulfonic acid of the general formula Z-S03H in which Z is a CI-Cm-alkyl radical, Cl-C20-haloalkyl radical, C5-C8-cycloalkyl radical, C6-C20-aryl radical or a C7-C20-aralkyl radical; a typical organic sulfonic acid of this kind is methanesulfonic acid.
According to measure (c), the polymerization catalyst used, however, is preferably a complex of boron trifluoride and a proton source. Suitable proton sources of this kind, which assume the function of an activator or moderator in the catalyst complex, are in particular ethers, especially C1- to C4-dialkyl ethers such as diethyl ether, and alcohols, especially low molecular weight monohydric aliphatic alcohols. In a particularly preferred embodiment, the polymerization catalyst used is a complex of boron trifluoride and a to Cralkanol, e.g.
methanol, ethanol, n-propanol or isopropanol. The proton sources used may also be mixtures of the ethers and/or alcohols mentioned.
The boron trifluoride and the proton source may be premixed and added to the polymerization reactor already as an active complex. Alternatively, however, the boron trifluoride [in gaseous or liquid form or in an inert solvent or diluent, for example dissolved in an inert solvent according to measure (b)] and the proton source may also be supplied separately to the polymerization medium.
The amount of polymerization catalyst to be used is guided substantially by the type of catalyst and by the reaction conditions, especially the reaction temperature and the desired molecular weight of the polymer. It can be determined on the basis of a few sample tests for the respective reaction system. In general, the polymerization catalyst is used in amounts of 0.0001 to 1% by weight, especially 0.0005 to 0.5% by weight, in particular 0.001 to 0.1% by weight, based in each case on the Lewis acid content or boron trifluoride content in the catalyst complex and on isobutene used.
2012/072643 A2, explicit reference being made here thereto. The iron halide, aluminum trihalide and aluminum alkyl halide complexes mentioned comprise, as well as the Lewis acid, a donor in the form of an organic compound having at least one ether function or a carboxylic ester function. This combination of Lewis acids, especially of boron trifluoride, iron halides, aluminum trihalides or aluminum alkyl halides, with organic sulfonic acids as initiators comprise at least one organic sulfonic acid of the general formula Z-S03H in which Z is a CI-Cm-alkyl radical, Cl-C20-haloalkyl radical, C5-C8-cycloalkyl radical, C6-C20-aryl radical or a C7-C20-aralkyl radical; a typical organic sulfonic acid of this kind is methanesulfonic acid.
According to measure (c), the polymerization catalyst used, however, is preferably a complex of boron trifluoride and a proton source. Suitable proton sources of this kind, which assume the function of an activator or moderator in the catalyst complex, are in particular ethers, especially C1- to C4-dialkyl ethers such as diethyl ether, and alcohols, especially low molecular weight monohydric aliphatic alcohols. In a particularly preferred embodiment, the polymerization catalyst used is a complex of boron trifluoride and a to Cralkanol, e.g.
methanol, ethanol, n-propanol or isopropanol. The proton sources used may also be mixtures of the ethers and/or alcohols mentioned.
The boron trifluoride and the proton source may be premixed and added to the polymerization reactor already as an active complex. Alternatively, however, the boron trifluoride [in gaseous or liquid form or in an inert solvent or diluent, for example dissolved in an inert solvent according to measure (b)] and the proton source may also be supplied separately to the polymerization medium.
The amount of polymerization catalyst to be used is guided substantially by the type of catalyst and by the reaction conditions, especially the reaction temperature and the desired molecular weight of the polymer. It can be determined on the basis of a few sample tests for the respective reaction system. In general, the polymerization catalyst is used in amounts of 0.0001 to 1% by weight, especially 0.0005 to 0.5% by weight, in particular 0.001 to 0.1% by weight, based in each case on the Lewis acid content or boron trifluoride content in the catalyst complex and on isobutene used.
6 The proton source can be used in a substoichiometric, stoichiometric or superstoichiometric amount in relation to the boron trifluoride. Typical molar ratios of proton source to boron trifluoride are in the range from 0.3:1 to 3:1, especially 0.5:1 to 2:1, in particular 0.7:1 to 1.3:1 (based in each case on one proton equivalent of the proton source). Just like the amount of reaction accelerator according to measure (d) and of chain length regulator according to measure (e), it is also possible for the amount of proton source according to measure (c) to influence the establishment of the molecular weight to be achieved in the isobutene homopolymer and also to serve for controlled establishment of the molecular weight thereof.
The isobutene homopolymers prepared by the process according to the invention preferably have a weight-average molecular weight (Mw) of 150 000 to 8 000 000, especially of 250 000 to 6 000 000, in particular of 400 000 to 5 000 000. Alternatively, they preferably have a number-average molecular weight (Me) (determined by gel permeation chromatography) of 25 000 to 2 000 000, more preferably of 45 000 to 1 500 000, especially of 55 000 to 1 000 000, in particular of 65 000 to 750 000.
In general, the isobutene homopolymers prepared by the process according to the invention have a polydispersity (PDI = Mw/Me) of 2 to 20, especially of 3 to 15, in particular of 5 to 10.
According to measure (a), the polymerization process according to the invention is performed in the liquid polymerization medium at temperatures of -80 C to -190 C. In a preferred embodiment, it is performed at temperatures close to the lower limit of the abovementioned temperature range, specifically at -130 C to -190 C, in particular at less than -160 C to -185 C, especially at -165 C to -180 C, in a typical procedure at -168 C to -173 C. In an alternative preferred embodiment, the process is performed at temperatures of -100 C to -150 C, preferably at -105 C to -147 C, in particular at -110 C to -140 C, especially at -115 C
to -135 C, in a typical procedure at -120 C to -130 C. The controlled low polymerization temperatures have an advantageous effect on the product properties. The temperature establishment in the precooling of the starting materials used, especially of the isobutene, can under some circumstances likewise influence the course of the polymerization and the results achieved; the isobutene to be used is cooled typically to temperatures of -70 C to -140 C, especially to -70 C to -100 C.
The reaction medium is advantageously cooled to the abovementioned temperatures by external cooling. In a preferred embodiment, therefore, measure (a) is executed by bringing the polymerization medium to the required low temperature and keeping it there during the polymerization by means of a separate cooling circuit. The separate cooling circuit, which in
The isobutene homopolymers prepared by the process according to the invention preferably have a weight-average molecular weight (Mw) of 150 000 to 8 000 000, especially of 250 000 to 6 000 000, in particular of 400 000 to 5 000 000. Alternatively, they preferably have a number-average molecular weight (Me) (determined by gel permeation chromatography) of 25 000 to 2 000 000, more preferably of 45 000 to 1 500 000, especially of 55 000 to 1 000 000, in particular of 65 000 to 750 000.
In general, the isobutene homopolymers prepared by the process according to the invention have a polydispersity (PDI = Mw/Me) of 2 to 20, especially of 3 to 15, in particular of 5 to 10.
According to measure (a), the polymerization process according to the invention is performed in the liquid polymerization medium at temperatures of -80 C to -190 C. In a preferred embodiment, it is performed at temperatures close to the lower limit of the abovementioned temperature range, specifically at -130 C to -190 C, in particular at less than -160 C to -185 C, especially at -165 C to -180 C, in a typical procedure at -168 C to -173 C. In an alternative preferred embodiment, the process is performed at temperatures of -100 C to -150 C, preferably at -105 C to -147 C, in particular at -110 C to -140 C, especially at -115 C
to -135 C, in a typical procedure at -120 C to -130 C. The controlled low polymerization temperatures have an advantageous effect on the product properties. The temperature establishment in the precooling of the starting materials used, especially of the isobutene, can under some circumstances likewise influence the course of the polymerization and the results achieved; the isobutene to be used is cooled typically to temperatures of -70 C to -140 C, especially to -70 C to -100 C.
The reaction medium is advantageously cooled to the abovementioned temperatures by external cooling. In a preferred embodiment, therefore, measure (a) is executed by bringing the polymerization medium to the required low temperature and keeping it there during the polymerization by means of a separate cooling circuit. The separate cooling circuit, which in
7 terms of design is usually implemented as an outer cooling jacket around the polymerization reactor, is generally operated with liquid nitrogen or liquefied air as the coolant.
The polymerization is performed generally at a pressure of 500 mbar to 5 bar, especially at a pressure of 800 mbar to 2 bar. Most advantageously and also most economically viably, the polymerization reactor is operated at or close to ambient pressure (standard pressure). A
slightly elevated pressure can bring advantages in the case of some of the possible inert solvents. Even though a mode of operation of the polymerization at elevated pressure is possible in principle, higher pressures, especially those over 5 bar, generally do not bring any additional advantages.
According to measure (b), particular inert solvents or mixtures of such inert solvents are used in the liquid polymerization medium. The term "inert solvents" shall be understood here to mean not just fluids in which isobutene dissolves homogeneously in a liquid phase but also fluids with which isobutene is immiscible and is present in the dispersed form. Suitable inert solvents of this kind are firstly C1 to 08 hydrocarbons, preferably C1 to 05 hydrocarbons, especially C2 to 04 hydrocarbons, which are typically saturated or monoethylenically unsaturated and generally have a linear or lightly branched structure. If they are ethylenically unsaturated, they must not of course themselves polymerize under the reaction conditions of the present invention; they normally have only primary and/or secondary olefinic carbon atoms. Typical examples of such Ci to C8 hydrocarbons are methane, ethane, ethene, propane, propene, n-butane, isobutane, n-pentane, 2-methylbutane, 2,3-dimethylbutane, 2-methylpentane, 3-methylpentane, 3-ethylpentane, 2,2-dimethylpentane, 2,3-dimethylpentane, 2,4-dimethylpentane, 2-methylhexane, 3-methylhexane, 3-ethyl-methylpentane, 2,2-dimethylhexane, 2,3-dimethylhexane, 3,3-dimethylhexane, 4-methylheptane, 2,2,3-trimethylpentane and 3-methylheptane. Other suitable inert solvents of this kind are halogenated Ci to 08 hydrocarbons, preferably halogenated Ci to hydrocarbons, especially fluorinated and/or chlorinated Ci to C8 or Ci to 05 hydrocarbons such as methyl chloride, methyl fluoride, difluoromethane, dichloromethane, fluoroethane, 1-fluoropropane, 1,1,1,2,3,3,3-heptafluoropropane, octafluoropropane or 1-fluorobutane;
particularly useful here are perfluorinated Ci to 08 or Ci to 05 hydrocarbons or those Ci to C8 or Ci to 05 hydrocarbons in which at least half of the hydrogen atoms have been replaced by fluorine atoms. It is also possible to use mixtures of Ci to C8 or Ci to 05 hydrocarbons, mixtures of halogenated Ci to C8 or Ci to C5 hydrocarbons or mixtures of one or more Ci to 08 or Cl to CS hydrocarbons and one or more halogenated Ci to 08 or C1 to 05 hydrocarbons.
In a preferred embodiment, as measure (b), the inert solvent used is ethane, ethene, propane, propene, n-butane, isobutane or a mixture thereof.
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The polymerization is performed generally at a pressure of 500 mbar to 5 bar, especially at a pressure of 800 mbar to 2 bar. Most advantageously and also most economically viably, the polymerization reactor is operated at or close to ambient pressure (standard pressure). A
slightly elevated pressure can bring advantages in the case of some of the possible inert solvents. Even though a mode of operation of the polymerization at elevated pressure is possible in principle, higher pressures, especially those over 5 bar, generally do not bring any additional advantages.
According to measure (b), particular inert solvents or mixtures of such inert solvents are used in the liquid polymerization medium. The term "inert solvents" shall be understood here to mean not just fluids in which isobutene dissolves homogeneously in a liquid phase but also fluids with which isobutene is immiscible and is present in the dispersed form. Suitable inert solvents of this kind are firstly C1 to 08 hydrocarbons, preferably C1 to 05 hydrocarbons, especially C2 to 04 hydrocarbons, which are typically saturated or monoethylenically unsaturated and generally have a linear or lightly branched structure. If they are ethylenically unsaturated, they must not of course themselves polymerize under the reaction conditions of the present invention; they normally have only primary and/or secondary olefinic carbon atoms. Typical examples of such Ci to C8 hydrocarbons are methane, ethane, ethene, propane, propene, n-butane, isobutane, n-pentane, 2-methylbutane, 2,3-dimethylbutane, 2-methylpentane, 3-methylpentane, 3-ethylpentane, 2,2-dimethylpentane, 2,3-dimethylpentane, 2,4-dimethylpentane, 2-methylhexane, 3-methylhexane, 3-ethyl-methylpentane, 2,2-dimethylhexane, 2,3-dimethylhexane, 3,3-dimethylhexane, 4-methylheptane, 2,2,3-trimethylpentane and 3-methylheptane. Other suitable inert solvents of this kind are halogenated Ci to 08 hydrocarbons, preferably halogenated Ci to hydrocarbons, especially fluorinated and/or chlorinated Ci to C8 or Ci to 05 hydrocarbons such as methyl chloride, methyl fluoride, difluoromethane, dichloromethane, fluoroethane, 1-fluoropropane, 1,1,1,2,3,3,3-heptafluoropropane, octafluoropropane or 1-fluorobutane;
particularly useful here are perfluorinated Ci to 08 or Ci to 05 hydrocarbons or those Ci to C8 or Ci to 05 hydrocarbons in which at least half of the hydrogen atoms have been replaced by fluorine atoms. It is also possible to use mixtures of Ci to C8 or Ci to 05 hydrocarbons, mixtures of halogenated Ci to C8 or Ci to C5 hydrocarbons or mixtures of one or more Ci to 08 or Cl to CS hydrocarbons and one or more halogenated Ci to 08 or C1 to 05 hydrocarbons.
In a preferred embodiment, as measure (b), the inert solvent used is ethane, ethene, propane, propene, n-butane, isobutane or a mixture thereof.
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8 In an alternative preferred embodiment, as measure (b), the inert solvent used is 1,1,1,2,3,3,3,-heptafluoropropane, octafluoropropane or a mixture thereof.
The weight ratio of isobutene to the inert solvents according to measure (b) in the polymerization reactor is generally 1:0.1 to 1:50, preferably 1:0.1 to 1:40, in particular 0.1:1 to 1:20, especially 1:0.5 to 1:10.
According to measure (d), the polymerization is performed in the presence of one or more reaction accelerators. Such a reaction accelerator is a compound which, under the selected polymerization conditions, influences and thus controls the catalytic activity of the boron trifluoride in the desired manner. Such reaction accelerators are saturated hydrocarbon compounds which comprise at least one oxygen atom, preferably as an ether oxygen atom or as part of a carbonyl function. In a preferred embodiment, as measure (d), the polymerization is performed in the presence of at least one reaction accelerator selected from ketones, aldehydes, ethers, acetals and hemiacetals. Typically, such reaction accelerators are low molecular weight compounds having 1 to 40, especially having 1 to 16 and in particular having 1 to 8 carbon atoms; the structure thereof may be open-chain or cyclic; they may be aliphatic, aromatic or heteroaromatic in nature.
Typical representatives of such reaction accelerators are ketones such as acetone, butanone, cyclohexanone, acetophenone or benzophenone, aldehydes such as formaldehyde, trioxane, paraformaldehyde, acetaldehyde, propionaldehyde, butyraldehyde, benzaldehyde, cyclohexylaldehyde or glyoxal, dialkyl ethers such as dimethyl ether, diethyl ether or di-n:butyl ether, cyclic ethers such as tetrahydrofuran or dioxane, and acetals and hemiacetals which are obtainable by reaction of the abovementioned ketones and aldehydes with alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, sec-butanol or tert-butanol. Very particular preference is given to using formaldehyde as such a reaction accelerator.
The reaction accelerators mentioned can usually be used in an advantageous manner together with one or more medium molecular weight alcohols, especially monohydric aliphatic, cycloaliphatic or araliphatic alcohols, in particular 04 to 010 alcohols, e.g. n-butanol, isobutanol, sec-butanol, tert-butanol, n-pentanol, n-hexanol, n-octanol, 2-ethylhexanol, n-decanol, 2-propylheptanol, cyclohexanol or benzyl alcohol. Firstly, such medium molecular weight alcohols ¨ similarly to the low molecular weight alcohols used as a proton source according to measure (c) ¨ act as activators or moderators in the catalyst complex, but usually with weaker activating action; secondly, they function as solvents for the reaction
The weight ratio of isobutene to the inert solvents according to measure (b) in the polymerization reactor is generally 1:0.1 to 1:50, preferably 1:0.1 to 1:40, in particular 0.1:1 to 1:20, especially 1:0.5 to 1:10.
According to measure (d), the polymerization is performed in the presence of one or more reaction accelerators. Such a reaction accelerator is a compound which, under the selected polymerization conditions, influences and thus controls the catalytic activity of the boron trifluoride in the desired manner. Such reaction accelerators are saturated hydrocarbon compounds which comprise at least one oxygen atom, preferably as an ether oxygen atom or as part of a carbonyl function. In a preferred embodiment, as measure (d), the polymerization is performed in the presence of at least one reaction accelerator selected from ketones, aldehydes, ethers, acetals and hemiacetals. Typically, such reaction accelerators are low molecular weight compounds having 1 to 40, especially having 1 to 16 and in particular having 1 to 8 carbon atoms; the structure thereof may be open-chain or cyclic; they may be aliphatic, aromatic or heteroaromatic in nature.
Typical representatives of such reaction accelerators are ketones such as acetone, butanone, cyclohexanone, acetophenone or benzophenone, aldehydes such as formaldehyde, trioxane, paraformaldehyde, acetaldehyde, propionaldehyde, butyraldehyde, benzaldehyde, cyclohexylaldehyde or glyoxal, dialkyl ethers such as dimethyl ether, diethyl ether or di-n:butyl ether, cyclic ethers such as tetrahydrofuran or dioxane, and acetals and hemiacetals which are obtainable by reaction of the abovementioned ketones and aldehydes with alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, sec-butanol or tert-butanol. Very particular preference is given to using formaldehyde as such a reaction accelerator.
The reaction accelerators mentioned can usually be used in an advantageous manner together with one or more medium molecular weight alcohols, especially monohydric aliphatic, cycloaliphatic or araliphatic alcohols, in particular 04 to 010 alcohols, e.g. n-butanol, isobutanol, sec-butanol, tert-butanol, n-pentanol, n-hexanol, n-octanol, 2-ethylhexanol, n-decanol, 2-propylheptanol, cyclohexanol or benzyl alcohol. Firstly, such medium molecular weight alcohols ¨ similarly to the low molecular weight alcohols used as a proton source according to measure (c) ¨ act as activators or moderators in the catalyst complex, but usually with weaker activating action; secondly, they function as solvents for the reaction
9 accelerators. When aldehydes or ketones are used as reaction accelerators, the abovementioned medium molecular weight alcohols, and also some of the low molecular weight alcohols mentioned, can form acetals or hemiacetals or ketals (ketone acetals) therewith, and these likewise act as reaction accelerators. If formaldehyde is used as a reaction accelerator, it is possible to use a corresponding alcoholic solution, e.g.
formaldehyde in isobutanol. If medium molecular weight alcohols of this kind are used, the weight ratio thereof relative to the reaction accelerator is generally 0.05:1 to 15:1, but preferably 0.1:1 to 5:1, especially 0.5:1 to 2.5:1, in particular 0.75:1 to 1.5:1.
The reaction accelerator itself is normally used in amounts of 0.0001 to 1% by weight, preferably 0.0003 to 0.75% by weight, especially 0.0005 to 0.5% by weight, in particular 0.001 to 0.1% by weight, based in each case on isobutene used.
According to measure (e), the polymerization is performed in the presence of at least one chain length regulator, which is normally an ethylenically unsaturated system and comprises one or more tertiary olefinic carbon atoms ¨ optionally in addition to one or more primary and/or secondary olefinic carbon atoms. Usually, such chain length regulators are mono- or polyethylenically unsaturated hydrocarbons having 5 to 30, especially having 5 to 20 and in particular having 5 to 16 carbon atoms; the structure thereof may be open-chain or cyclic.
Typical representatives of such chain length regulators are isoprene (2-methyl-1,3-butadiene), 2-methyl-2-butene, diisobutene, triisobutene, tetraisobutene and 1-methylcyclohexene. In a preferred embodiment, as measure (e), the polymerization is performed in the presence of isoprene and/or diisobutene as chain length regulators.
Diisobutene (isooctene) is typically understood to mean the isomer mixture of 2,4,4-trimethyl-1-pentene and 2,4,4-trimethy1-2-pentene; the individually used 2,4,4-trimethy1-1-pentene and 2,4,4-trimethy1-2-pentene isomers also of course likewise act as chain length regulators according to measure (e). Through the amount of the chain length regulators used in accordance with the invention, it is possible in a simple manner to adjust the molecular weight of isobutene homopolymers obtained: the higher the amount of chain length regulators, the lower the molecular weight will generally be. The chain length regulator typically controls the molecular weight by being incorporated into the polymer chain at an earlier or later stage and thus leading to chain termination at this site.
The chain length regulator is used normally in amounts of 0.0001 to 2% by weight, especially 0.0005 to 1% by weight, in particular 0.001 to 0.5% by weight, based in each case on isobutene used.
The process according to the invention for preparing isobutene homopolymers ¨
including the subsequent workup steps ¨ can be performed batchwise or continuously.
The polymerization reactors used for the process according to the invention may in principle 5 be all batchwise or continuous reactor types suitable for such liquid phase polymerizations, for example stirred tanks, stirred tank cascades, kneaders, extruders, tubular reactors or loop reactors.
It is advantageous to perform the process according to the invention at high conversions, if at
formaldehyde in isobutanol. If medium molecular weight alcohols of this kind are used, the weight ratio thereof relative to the reaction accelerator is generally 0.05:1 to 15:1, but preferably 0.1:1 to 5:1, especially 0.5:1 to 2.5:1, in particular 0.75:1 to 1.5:1.
The reaction accelerator itself is normally used in amounts of 0.0001 to 1% by weight, preferably 0.0003 to 0.75% by weight, especially 0.0005 to 0.5% by weight, in particular 0.001 to 0.1% by weight, based in each case on isobutene used.
According to measure (e), the polymerization is performed in the presence of at least one chain length regulator, which is normally an ethylenically unsaturated system and comprises one or more tertiary olefinic carbon atoms ¨ optionally in addition to one or more primary and/or secondary olefinic carbon atoms. Usually, such chain length regulators are mono- or polyethylenically unsaturated hydrocarbons having 5 to 30, especially having 5 to 20 and in particular having 5 to 16 carbon atoms; the structure thereof may be open-chain or cyclic.
Typical representatives of such chain length regulators are isoprene (2-methyl-1,3-butadiene), 2-methyl-2-butene, diisobutene, triisobutene, tetraisobutene and 1-methylcyclohexene. In a preferred embodiment, as measure (e), the polymerization is performed in the presence of isoprene and/or diisobutene as chain length regulators.
Diisobutene (isooctene) is typically understood to mean the isomer mixture of 2,4,4-trimethyl-1-pentene and 2,4,4-trimethy1-2-pentene; the individually used 2,4,4-trimethy1-1-pentene and 2,4,4-trimethy1-2-pentene isomers also of course likewise act as chain length regulators according to measure (e). Through the amount of the chain length regulators used in accordance with the invention, it is possible in a simple manner to adjust the molecular weight of isobutene homopolymers obtained: the higher the amount of chain length regulators, the lower the molecular weight will generally be. The chain length regulator typically controls the molecular weight by being incorporated into the polymer chain at an earlier or later stage and thus leading to chain termination at this site.
The chain length regulator is used normally in amounts of 0.0001 to 2% by weight, especially 0.0005 to 1% by weight, in particular 0.001 to 0.5% by weight, based in each case on isobutene used.
The process according to the invention for preparing isobutene homopolymers ¨
including the subsequent workup steps ¨ can be performed batchwise or continuously.
The polymerization reactors used for the process according to the invention may in principle 5 be all batchwise or continuous reactor types suitable for such liquid phase polymerizations, for example stirred tanks, stirred tank cascades, kneaders, extruders, tubular reactors or loop reactors.
It is advantageous to perform the process according to the invention at high conversions, if at
10 all possible at full conversion or near full conversion, for example at a conversion of the isobutene used to the desired product of 85% to 100%, especially of 90% to 100%. However, it is also possible ¨ especially in continuous mode ¨ to perform the process according to the invention with partial conversion, for example at a conversion of the isobutene used to the desired product of 10% to 85%, especially of 30% to 60%. In a preferred embodiment, the polymerization conditions for the process according to the invention are selected such that the isobutene used is converted in the polymerization reactor with a conversion of at least 90%, especially of at least 95%, in particular of at least 99%, to isobutene homopolymers having a weight-average molecular weight of 75 000 to 10 000 000.
In an advantageous execution of the process according to the invention, the isobutene feedstock or an isobutenic hydrocarbon mixture is premixed in a separate vessel together with the proton source, especially a C1- to C3-alkanol, and together with one or more reaction accelerators, especially selected from ketones, aldehydes, ethers, acetals and hemiacetals, and/or one or more chain length regulators, especially selected from isoprene and diisobutene, and added in the polymerization reactor to the inert solvent which comprises the boron trifluoride and has been cooled to polymerization temperature. It is also particularly advantageous to cool this mixture prior to addition to the polymerization reactor. This isobutenic mixture is added to the polymerization reactor such that the external cooling allows the desired polymerization temperature to be kept constant. Rapid and complete mixing of the isobutene into the continuous phase is crucial for effective temperature control and hence for the success of the process.
Evaporating nitrogen from the external cooling can then either be liquefied again in a closed circuit or ¨ without needing to undertake purification ¨ passed into the environment. In the case of renewed liquefaction of the recycled nitrogen stream, the low temperature of the evaporated nitrogen can be utilized advantageously and thus recovered. If the recycling is omitted, the refrigeration energy of the gaseous nitrogen can be utilized for other cooling purposes, for example for the cooling of the degassed end product.
In an advantageous execution of the process according to the invention, the isobutene feedstock or an isobutenic hydrocarbon mixture is premixed in a separate vessel together with the proton source, especially a C1- to C3-alkanol, and together with one or more reaction accelerators, especially selected from ketones, aldehydes, ethers, acetals and hemiacetals, and/or one or more chain length regulators, especially selected from isoprene and diisobutene, and added in the polymerization reactor to the inert solvent which comprises the boron trifluoride and has been cooled to polymerization temperature. It is also particularly advantageous to cool this mixture prior to addition to the polymerization reactor. This isobutenic mixture is added to the polymerization reactor such that the external cooling allows the desired polymerization temperature to be kept constant. Rapid and complete mixing of the isobutene into the continuous phase is crucial for effective temperature control and hence for the success of the process.
Evaporating nitrogen from the external cooling can then either be liquefied again in a closed circuit or ¨ without needing to undertake purification ¨ passed into the environment. In the case of renewed liquefaction of the recycled nitrogen stream, the low temperature of the evaporated nitrogen can be utilized advantageously and thus recovered. If the recycling is omitted, the refrigeration energy of the gaseous nitrogen can be utilized for other cooling purposes, for example for the cooling of the degassed end product.
11 As an alternative to liquid nitrogen or liquefied air, it is also possible when working within the range of a polymerization temperature of -100 C to -150 C to work with other external coolants, for example based on halogenated hydrocarbons.
The isobutene homopolymers which have a weight-average molecular weight of 75 000 to 000 000 and are prepared in the process according to the invention are worked up typically by discharging the product from the polymerization reactor and ¨
optionally after a suitable pretreatment ¨ by thermal purification of the product. The discharge is 10 advantageously effected at very low temperatures. The discharge from the reactor can be undertaken, for example, with the aid of a mechanical discharge device such as a discharge screw. In a preferred embodiment, which is of significance especially in the case of industrial scale execution of the process according to the invention, the isobutene homopolymers obtained in the polymerization reactor are discharged from the polymerization reactor at temperatures of less than -80 C and subjected to a thermal purification process at temperatures of more than +80 C.
The thermal purification after the discharge of the product from the polymerization reactor is advantageously effected, in the case of industrial scale execution of the process according to the invention, by use of one or more extruders. In this case, the isobutene homopolymers are heated to temperatures of more than 80 C, especially more than 100 C. The mechanical action of the extruder shafts and of any internals in the extruder constantly renews the inner surface for better degassing of the volatile constituents in the product, such as residual monomers and solvents. The degassing and the purification of the product can be facilitated by applying a vacuum; more particularly, a pressure of less than 700 mbar is employed for this purpose, especially of less than 200 mbar and in particular of less than 100 mbar.
It is possible in principle to use all customary single-shaft and twin-shaft and multishaft extruders for the thermal purification of the isobutene homopolymers obtained.
In the case of twin-shaft and multishaft extruders, the shafts may work in a corotatory or contrarotatory manner. The shafts in single-shaft and multishaft extruders are normally equipped with kneading and/or conveying elements. These apparatuses are generally self-cleaning. The shaft speeds are generally in the range from 10 to 500, and especially from 15 to 350 revolutions per minute. In a specific design, the shafts may be configured as screw shafts whose channels intermesh and whose internal shaft diameter is preferably constant over the entire length. Preferred construction materials for the extruders described are steels or stainless steels. It is also advantageous to introduce an inert gas, for example nitrogen, into one or more segments of the extruder in order to promote the degassing operation.
=
The isobutene homopolymers which have a weight-average molecular weight of 75 000 to 000 000 and are prepared in the process according to the invention are worked up typically by discharging the product from the polymerization reactor and ¨
optionally after a suitable pretreatment ¨ by thermal purification of the product. The discharge is 10 advantageously effected at very low temperatures. The discharge from the reactor can be undertaken, for example, with the aid of a mechanical discharge device such as a discharge screw. In a preferred embodiment, which is of significance especially in the case of industrial scale execution of the process according to the invention, the isobutene homopolymers obtained in the polymerization reactor are discharged from the polymerization reactor at temperatures of less than -80 C and subjected to a thermal purification process at temperatures of more than +80 C.
The thermal purification after the discharge of the product from the polymerization reactor is advantageously effected, in the case of industrial scale execution of the process according to the invention, by use of one or more extruders. In this case, the isobutene homopolymers are heated to temperatures of more than 80 C, especially more than 100 C. The mechanical action of the extruder shafts and of any internals in the extruder constantly renews the inner surface for better degassing of the volatile constituents in the product, such as residual monomers and solvents. The degassing and the purification of the product can be facilitated by applying a vacuum; more particularly, a pressure of less than 700 mbar is employed for this purpose, especially of less than 200 mbar and in particular of less than 100 mbar.
It is possible in principle to use all customary single-shaft and twin-shaft and multishaft extruders for the thermal purification of the isobutene homopolymers obtained.
In the case of twin-shaft and multishaft extruders, the shafts may work in a corotatory or contrarotatory manner. The shafts in single-shaft and multishaft extruders are normally equipped with kneading and/or conveying elements. These apparatuses are generally self-cleaning. The shaft speeds are generally in the range from 10 to 500, and especially from 15 to 350 revolutions per minute. In a specific design, the shafts may be configured as screw shafts whose channels intermesh and whose internal shaft diameter is preferably constant over the entire length. Preferred construction materials for the extruders described are steels or stainless steels. It is also advantageous to introduce an inert gas, for example nitrogen, into one or more segments of the extruder in order to promote the degassing operation.
=
12 The process according to the invention has the advantage that the isobutene homopolymers obtained have only a low solubility in the solvent used (hydrocarbons and/or halogenated hydrocarbons) ¨ and this is especially true at low temperatures ¨ and hence precipitate out substantially in solid form. This precipitated solid has no tendency whatsoever to stick at the low temperatures used, and so the crude product can be discharged and processed further without difficulty since nowhere in the intake region of the product from the reactor into the workup section do temperatures exceed the glass transition temperature of the polymer.
The examples which follow are intended to illustrate the present invention without restricting it.
Examples 1 to 12 A 1 liter three-neck flask with mechanical stirrer, inlet tube for dry, gaseous nitrogen for inertization, a thermocouple for temperature monitoring and a coolable dropping funnel was inertized with the aid of liquid nitrogen (in a Dewar flask positioned around the flask) and then cooled to -100 C. Subsequently, 300 ml of liquid propane was initially charged in the flask under a nitrogen atmosphere and 0.1 g of gaseous boron trifluoride was introduced.
The Dewar flask under the flask stood on a height-adjustable lab jack.
Variation of the fill level in the Dewar flask allowed the desired polymerization temperature T to be established without difficulty.
94.0 g (1.68 mol) of liquid isobutene were introduced into the dropping funnel cooled with dry ice (approx. -78 C) or liquid nitrogen (approx. -130 C). Subsequently, the amounts of methanol, isobutanol, formaldehyde (which had been freshly produced from paraformaldehyde and was present dissolved in the methanol/isobutanol mixture) and diisobutene specified below in each case were metered in and mixed with the isobutene in the dropping funnel.
After the attainment of the desired polymerization temperature T in the flask, the dropwise addition of the dropping funnel contents was commenced while stirring. Each droplet reacted immediately and a fine solid was obtained to an increasing degree. The desired reaction temperature T was kept constant over the entire dropwise addition time by raising or lowering the Dewar flask by means of the jack and adding more liquid nitrogen.
The examples which follow are intended to illustrate the present invention without restricting it.
Examples 1 to 12 A 1 liter three-neck flask with mechanical stirrer, inlet tube for dry, gaseous nitrogen for inertization, a thermocouple for temperature monitoring and a coolable dropping funnel was inertized with the aid of liquid nitrogen (in a Dewar flask positioned around the flask) and then cooled to -100 C. Subsequently, 300 ml of liquid propane was initially charged in the flask under a nitrogen atmosphere and 0.1 g of gaseous boron trifluoride was introduced.
The Dewar flask under the flask stood on a height-adjustable lab jack.
Variation of the fill level in the Dewar flask allowed the desired polymerization temperature T to be established without difficulty.
94.0 g (1.68 mol) of liquid isobutene were introduced into the dropping funnel cooled with dry ice (approx. -78 C) or liquid nitrogen (approx. -130 C). Subsequently, the amounts of methanol, isobutanol, formaldehyde (which had been freshly produced from paraformaldehyde and was present dissolved in the methanol/isobutanol mixture) and diisobutene specified below in each case were metered in and mixed with the isobutene in the dropping funnel.
After the attainment of the desired polymerization temperature T in the flask, the dropwise addition of the dropping funnel contents was commenced while stirring. Each droplet reacted immediately and a fine solid was obtained to an increasing degree. The desired reaction temperature T was kept constant over the entire dropwise addition time by raising or lowering the Dewar flask by means of the jack and adding more liquid nitrogen.
13 Once the entire dropping funnel contents have been added dropwise, the contents of the flask were allowed to thaw, in the course of which the propane solvent (boiling point: -42 C) evaporated. Subsequently, the crude product which had become tacky at room temperature was removed and it was freed of the residual solvent by heating in a drying cabinet (temperature: 160 C at 30 mbar, duration: 2 h). Thereafter, it was possible to determine the analytical data of the isobutene homopolymer obtained.
The table below indicates the temperatures, the amounts used and the analytical data of the products obtained in each case.
Example No. 1 2 3 4 5 6 Polymerization temp. T -170 C -170 C -170 C -170 C -170 C -lsobutene precooling -78 C -78 C -78 C -130 C -130 C -130 C
Amount of methanol 0.15 ml 0.15 ml 0.15 ml 0.15 ml 0.15 ml 0.15 ml Amount of isobutanol 0.05 ml 0.05 ml 0.05 ml 0.05 ml 0.05 ml 0.05 ml Amount of formaldehyde 0.05 g 0.05 g 0.05 g 0.05 g 0.05 g 0.05 g Amount of diisobutene 0.01 ml 0.02 ml 0.05 ml 0 ml 0.01 ml 0.05 ml Molecular weight Mw 824000 796000 483000 5157000 3831000 2055000 Molecular weight Mn 123000 117000 68000 586000 421000 Polydispersity D 6.7 6.8 7.1 8.8 9.1 9.3 Example No. 7 8 9 10 11 12 Polymerization temp. T -150 C -140 C -130 C -120 C -110 C -lsobutene precooling -78 C -78 C -78 C -78 C -78 C -78 C
Amount of methanol 0.15 ml 0.15 ml 0.15 ml 0.15 ml 0.15 ml 0.15 ml Amount of isobutanol 0.05 ml 0.05 ml 0.50 ml 0.50 ml 0.05 ml 0.05 ml Amount of formaldehyde 0.05 g 0.05 g 0.05 g 0.50 g 0.50 g 0.50 g Amount of diisobutene 0.01 ml 0.01 ml 0.01 ml 0.01 ml 0.01 ml 0.01 ml Molecular weight Mw 823000 811000 803000 803000 766000 715000 Molecular weight Mr, 121000 121000 110000 103000 88000 73000 Polydispersity D 6.8 6.7 7.3 7.8 8.7 9.8
The table below indicates the temperatures, the amounts used and the analytical data of the products obtained in each case.
Example No. 1 2 3 4 5 6 Polymerization temp. T -170 C -170 C -170 C -170 C -170 C -lsobutene precooling -78 C -78 C -78 C -130 C -130 C -130 C
Amount of methanol 0.15 ml 0.15 ml 0.15 ml 0.15 ml 0.15 ml 0.15 ml Amount of isobutanol 0.05 ml 0.05 ml 0.05 ml 0.05 ml 0.05 ml 0.05 ml Amount of formaldehyde 0.05 g 0.05 g 0.05 g 0.05 g 0.05 g 0.05 g Amount of diisobutene 0.01 ml 0.02 ml 0.05 ml 0 ml 0.01 ml 0.05 ml Molecular weight Mw 824000 796000 483000 5157000 3831000 2055000 Molecular weight Mn 123000 117000 68000 586000 421000 Polydispersity D 6.7 6.8 7.1 8.8 9.1 9.3 Example No. 7 8 9 10 11 12 Polymerization temp. T -150 C -140 C -130 C -120 C -110 C -lsobutene precooling -78 C -78 C -78 C -78 C -78 C -78 C
Amount of methanol 0.15 ml 0.15 ml 0.15 ml 0.15 ml 0.15 ml 0.15 ml Amount of isobutanol 0.05 ml 0.05 ml 0.50 ml 0.50 ml 0.05 ml 0.05 ml Amount of formaldehyde 0.05 g 0.05 g 0.05 g 0.50 g 0.50 g 0.50 g Amount of diisobutene 0.01 ml 0.01 ml 0.01 ml 0.01 ml 0.01 ml 0.01 ml Molecular weight Mw 823000 811000 803000 803000 766000 715000 Molecular weight Mr, 121000 121000 110000 103000 88000 73000 Polydispersity D 6.8 6.7 7.3 7.8 8.7 9.8
Claims (14)
1. A process for preparing isobutene homopolymers having a weight-average molecular weight of 75 000 to 10 000 000 by polymerization of isobutene in the liquid phase in an inert solvent in the presence of a polymerization catalyst based on Lewis acids, which comprises, in a polymerization reactor, at the same time (a) performing the polymerization at temperatures of -80°C to -190°C, (b) using, as an inert solvent, one or more C1 to C8 hydrocarbons or one or more halogenated C1 to C8 hydrocarbons or a mixture thereof and (c) using, as a polymerization catalyst, a Lewis acid complex based on boron trifluoride, on iron halides, on aluminum trihalides or on aluminum alkyl halides or a Lewis acid in combination with organic sulfonic acids as initiators, and additionally (d) performing the polymerization in the presence of at least one reaction accelerator in the form of an ethylenically saturated hydrocarbon compound comprising at least one oxygen atom and no abstractable proton, and/or (e) performing the polymerization in the presence of at least one chain length regulator comprising at least one tertiary olefinic carbon atom.
2. The process according to claim 1, wherein measures (d) and (e) are both performed.
3. The process according to claim 1 or 2, wherein, as measure (a), the polymerization is performed at temperatures of less than -160°C to -185°C.
4. The process according to claim 1 or 2, wherein, as measure (a), the polymerzation is performed at temperatures of -110°C to -140°C.
5. The process according to claims 1 to 4, wherein measure (a) is executed by bringing the polymerization medium to the required low temperature and keeping it there during the polymerization by means of a separate cooling circuit.
6. The process according to claims 1 to 5, wherein, as measure (b), the inert solvent used is ethane, ethene, propane, propene, n-butane, isobutane or a mixture thereof.
7. The process according to claims 1 to 5, wherein, as measure (b), the inert solvent used is 1,1,1,2,3,3,3-heptafluoropropane, octafluoropropane or a mixture thereof.
8. The process according to claims 1 to 7, wherein, as measure (c), the polymerization catalyst used is a complex of boron trifluoride and a proton source.
9. The process according to claim 8, wherein, as measure (c), the polymerization catalyst used is a complex of boron trifluoride and a C1- to C4-alkanol.
10. The process according to claims 1 to 9, wherein, as measure (d), the polymerization is performed in the presence of at least one reaction accelerator selected from ketones, aldehydes, ethers, acetals and hemiacetals.
11. The process according to claims 1 to 10, wherein, as measure (e), the polymerization is performed in the presence of isoprene and/or diisobutene as chain length regulators.
12. The process according to claims 1 to 11, wherein the polymerization conditions are selected such that the isobutene used is converted in the polymerization reactor with a conversion of at least 90% to isobutene homopolymers having a weight-average molecular weight of 75 000 to 10 000 000.
13. The process according to claims 1 to 12, wherein the isobutene homopolymers obtained in the polymerization reactor are discharged from the polymerization reactor at temperatures of less than -80°C and subjected to a thermal purification process at temperatures of more than +80°C.
14. The process according to claim 13, wherein the thermal purification process is executed using one or more extruders.
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| US20130102748A1 (en) * | 2011-10-21 | 2013-04-25 | Hannah Maria Koenig | Process for preparing isobutene homopolymers or copolymers |
| US10889534B2 (en) | 2015-07-10 | 2021-01-12 | Uop Llc | Alkylation processes using liquid Lewis acid catalysts |
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|---|---|---|---|---|
| CN107522816B (en) * | 2017-09-26 | 2021-07-09 | 青岛瑞林材料科技有限公司 | Method for synthesizing high cis-diene polymer |
| CN107522817A (en) * | 2017-09-26 | 2017-12-29 | 青岛瑞林材料科技有限公司 | A kind of preparation method of high-cis polydiene hydrocarbon |
| CN107652381B (en) * | 2017-09-26 | 2021-07-09 | 青岛瑞林材料科技有限公司 | Preparation method of high cis-diene polymer |
| CN107501472A (en) * | 2017-09-26 | 2017-12-22 | 青岛瑞林材料科技有限公司 | A kind of synthetic method of high-cis diene polymer |
| CN107602747B (en) * | 2017-09-26 | 2021-01-12 | 青岛瑞林材料科技有限公司 | Synthesis method of high cis-polydiene |
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| GB590595A (en) * | 1944-03-14 | 1947-07-23 | Standard Oil Dev Co | Improved process and apparatus for the polymerisation of iso-olefins |
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| FR2117121A5 (en) * | 1970-12-12 | 1972-07-21 | Basf Ag | |
| SU478022A1 (en) * | 1973-12-07 | 1975-07-25 | Предприятие П/Я А-7942 | The method of regulating the process of low-temperature polymerization of isobutylene |
| DE3332629A1 (en) * | 1983-09-09 | 1985-03-28 | Hermann Berstorff Maschinenbau Gmbh, 3000 Hannover | METHOD AND DEVICE FOR POWDERING POLYMERS |
| DE3404764A1 (en) * | 1984-02-10 | 1985-08-14 | Basf Ag, 6700 Ludwigshafen | METHOD FOR POLYMERIZING ISOBUTYLENE |
| US4946899A (en) * | 1988-12-16 | 1990-08-07 | The University Of Akron | Thermoplastic elastomers of isobutylene and process of preparation |
| WO2000011040A1 (en) * | 1998-08-25 | 2000-03-02 | Nippon Petrochemicals Company, Limited | Process for producing butene polymer |
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| DE102005048698A1 (en) * | 2005-10-11 | 2007-04-12 | Basf Ag | Production of polyisobutene, preferably of high molecular weight, involves polymerization by contacting isobutene droplets with Lewis acid containing halogen as catalyst using inert diluent, preferably as lower liquid reservoir zone |
| WO2007113196A1 (en) | 2006-04-05 | 2007-10-11 | Basf Se | Process for preparing high molecular weight isobutene homopolymers by polymerization in an apparatus with mixing and conveying properties |
| CN101602823B (en) * | 2008-06-13 | 2011-04-20 | 中国石油化工股份有限公司 | Cationic polymerization initiation system and application thereof |
| EP2646478A2 (en) | 2010-11-30 | 2013-10-09 | Basf Se | Production of isobutylene homopolymer or copolymer derivatives |
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- 2013-02-15 WO PCT/EP2013/053042 patent/WO2013120984A1/en active Application Filing
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- 2017-07-21 JP JP2017141991A patent/JP2017186577A/en not_active Withdrawn
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20130102748A1 (en) * | 2011-10-21 | 2013-04-25 | Hannah Maria Koenig | Process for preparing isobutene homopolymers or copolymers |
| US9458262B2 (en) * | 2011-10-21 | 2016-10-04 | Basf Se | Process for preparing isobutene homopolymers or copolymers |
| US10889534B2 (en) | 2015-07-10 | 2021-01-12 | Uop Llc | Alkylation processes using liquid Lewis acid catalysts |
Also Published As
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| CN104136470B (en) | 2016-08-24 |
| KR20140122757A (en) | 2014-10-20 |
| EP2814851A1 (en) | 2014-12-24 |
| JP2017186577A (en) | 2017-10-12 |
| KR101974337B1 (en) | 2019-05-02 |
| MY168940A (en) | 2019-01-10 |
| JP2015507069A (en) | 2015-03-05 |
| CN104136470A (en) | 2014-11-05 |
| SG11201403863YA (en) | 2014-10-30 |
| CA2863836C (en) | 2020-06-30 |
| WO2013120984A1 (en) | 2013-08-22 |
| SG10201606861XA (en) | 2016-10-28 |
| JP6234382B2 (en) | 2017-11-22 |
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