EP1368391A1 - Procede de production d'elastomeres en continu - Google Patents

Procede de production d'elastomeres en continu

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Publication number
EP1368391A1
EP1368391A1 EP02708315A EP02708315A EP1368391A1 EP 1368391 A1 EP1368391 A1 EP 1368391A1 EP 02708315 A EP02708315 A EP 02708315A EP 02708315 A EP02708315 A EP 02708315A EP 1368391 A1 EP1368391 A1 EP 1368391A1
Authority
EP
European Patent Office
Prior art keywords
reactors
reactor
elastomers
polymerization
residence time
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP02708315A
Other languages
German (de)
English (en)
Inventor
Thomas Knauf
Josef-Werner Naunheim
Klaus Wiemann
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Lanxess Deutschland GmbH
Original Assignee
Bayer AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bayer AG filed Critical Bayer AG
Publication of EP1368391A1 publication Critical patent/EP1368391A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00—Processes of polymerisation
    • C08F2/04—Polymerisation in solution
    • C08F2/06—Organic solvent
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F36/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F36/02—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
    • C08F36/04—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated

Definitions

  • the present invention relates to a continuous process for the production of elastomers based on conjugated dienes or based on conjugated
  • Reactors is higher than in the first reactor.
  • the object of the present invention is therefore, inter alia. To improve the economy of the previous processes for the preparation of diene polymers, as well as the product quality of the polymers obtained.
  • the present invention therefore relates to a continuous process for the preparation of elastomers based on conjugated dienes or based on conjugated dienes and vinylaromatic compounds or based on alkenes, which is characterized in that the polymerization is carried out in the presence of an inert solvent and in the presence of polymerization catalysts in at least two reactors connected in series, the residence time of the monomers used and of the elastomers formed in the first reactor being set such that the residence time of the monomers used and the elastomers formed in the first reactor at the residence time of the ones used
  • Monomers and the elastomers formed in the remaining reactors is in the range from 1: 1 to 4: 1, the temperature gradient in the first reactor is ⁇ 25 ° C. and the temperature in the individual reactors during the polymerization is in the range from 0 to 140 ° C. .
  • the residence time of the monomers used and the elastomers formed in the first reactor is preferably set such that the residence time of the monomers used and the elastomers formed in the first reactor relative to the residence time of the monomers used and the elastomers formed in the remaining reactors is in the range of 1 : 1 to 3: 1, in particular in the range from 1.1: 1 to 2.5: 1, and very particularly preferably in the range from 1.2: 1 to 2: 1. More than For two reactors connected in series, it is important for the overall residence time ratio that the residence time of the monomers and elastomers in the remaining reactors - this includes the reactors which are connected downstream of the first reactor - is divided in such a way that the claimed ratio always results. The distribution of the respective residence times in the remaining reactors can therefore be chosen as desired, and the most favorable distribution can easily be determined by appropriate preliminary tests.
  • the type of reactors used, the type of catalysts and monomers used play a role in the distribution of the residence times.
  • the process according to the invention it is possible to distribute the residence time of the monomers used and the elastomers formed instead of over a first reactor over a plurality of reactors connected in parallel, which are then to be regarded as the first reactor.
  • a first reactor instead of a first reactor, two or three reactors can be connected in parallel and thus serve as the first reactor.
  • additional reactors are used which are then connected in series.
  • the number of reactors connected in series depends, among other things. from economic considerations of the process and can be 2 to 10, preferably 2 to 7, in particular 2 to 3, additional reactors.
  • the temperature gradient in the first reactor or the first reactors connected in parallel is ⁇ 25 ° C., preferably ⁇ 15 ° C., in particular ⁇ 10 ° C.
  • the temperature gradient is to be understood as the temperature difference in the first reactor which results from the measurement of the temperature at the inlet of the monomers used and at the outlet of the product stream coming from the first reactor or the first reactors, which essentially consists of solvents, elastomers formed and used Monomers.
  • the temperature during the polymerization in the individual reactors is preferably in the range from 10 to 130 ° C., in particular 20 to 120 ° C.
  • the known polymerization reactors can be used as reactors in the process according to the invention, in particular stirred reactors are used.
  • the process according to the invention is carried out in the inert organic solvents known therefor, for example butanes, butenes, pentaes, hexanes, heptanes, methylcyclopentane or cyclohexane.
  • inert organic solvents known therefor, for example butanes, butenes, pentaes, hexanes, heptanes, methylcyclopentane or cyclohexane.
  • Aromatic solvents such as benzene, toluene or ethylbenzene can also be used.
  • the solvents can be used either individually or in a mixture with one another.
  • the amount of solvent used is not critical. The cheapest amount can be determined by appropriate preliminary tests and depends, among other things. on economic considerations.
  • Dienes are used, which are common for the production of appropriate elastomers. Examples include: 1,3-butadiene, isoprene, piperylene, 1,3-hexadiene, 1,3-octadiene and 2-phenyl-1,3-butadiene, preferably 1,3-butadiene and isoprene.
  • the known vinylaromatic compounds which can be copolymerized together with the conjugated diene are also suitable as vinylaromatic compounds.
  • Examples include styrene, p-methylstyrene, ⁇ -methylstyrene, 3,5-dimethylstyrene, vinylnaphthalene, p-tert-butylstyrene, divinylstyrene and diphenylethylene, in particular styrene.
  • the amount of vinylaromatic compounds used is usually 5 to 55% by weight, preferably 10 to 45% by weight, and the amount of conjugated dienes used is correspondingly 45 to 95% by weight. -%, preferably 55 to 90 wt .-%.
  • alkenes such as ethylene and propylene
  • alkenes can also be used in the process according to the invention to build up the elastomers.
  • alkenes such as ethylene and propylene
  • non-conjugated polyenes such as ethylene norbornene, vinylidene norbornene, dicyclopentadiene, 2-methyl-l, 5-hexadiene,
  • Polyenes is usually up to 15% by weight, preferably 10% by weight, the proportion of alkenes correspondingly complements each other to 100% by weight.
  • the amount of ethylene and propylene monomers is generally about 20 to 80 wt .-% (ethylene) and 80 to 20 wt .-% (propylene) in the production of corresponding terpolymers.
  • the process according to the invention can be carried out in the presence of catalysts or initiators known for the polymerization of the monomers mentioned.
  • the process according to the invention is not restricted to a specific catalyst or specific catalysts or a specific catalyst or initiator system. All known Ziegler-Natta catalysts or catalyst systems are therefore also suitable, as are the known anionic initiators.
  • Ziegler-Natta catalysis with appropriate catalysts and anionic polymerization with appropriate initiators are explained in more detail by W. Hoffmann, in Rubber Technologie Handbook, Hanser Publishers (Carl Hanser Verlag) Kunststoff, Vienna, New York, pp. 52-67, 1989 or in Polymer Synthesis, Weg and Wepf Verlag Basel, Heidelberg, New York, 1986, pp. 124-132 and pp. 176-181.
  • Ziegler-Natta catalysts are systems based on titanium, cobalt, vanadium and nickel compounds and systems based on compounds of rare earth metals.
  • the various types of Ziegler-Natta catalysts can be used both individually and as a mixture with one another.
  • Ziegler-Natta catalysts based on rare earth compounds such as cerium, lanthanum, praseodymium, gadolinium or neodymium compounds, which are soluble in hydrocarbons, are preferably used.
  • the corresponding salts of the rare earth metals are particularly preferably used as Ziegler-Natta catalysts, such as neodymium carboxylates, in particular neodymium neodecanoate.
  • the Ziegler-Natta catalysts that can be used also include catalyst systems based on metallocenes, such as described in the following literature:
  • a common Ziegler-Natta catalyst system is based, for example, on cobalt octoate as component A, on diethyl aluminum chloride as component B and on water as component C in systems composed of three components (see further details under US Pat. No. 5,397,851).
  • the above-mentioned Ziegler-Natta catalysts or the catalyst systems based on Ziegler-Natta catalysts with corresponding cocatalysts are, for example — as mentioned — described in W. Hoffmann, Rubber Technology
  • the polymerization of the unsaturated monomers is carried out in the presence of a Ziegler-Natta catalyst, as described in German patent application No. 19951841.6.
  • hal stands for fluorine, chlorine and bromine
  • R represents hydrogen or a vinyl group
  • the Ziegler-Natta catalysts based on rare earth compounds are generally used in the process in amounts of about 0.01 to 1 mmol, preferably 0.03 to 0.2 mmol, based on 100 g of polymer.
  • the amount of catalysts to be used depends in particular on the type of catalysts to be used and the desired rubber properties.
  • lithium metal-containing initiators are used as anionic initiators in the process according to the invention.
  • examples include n-butyllithium, sec-butyllithium, tert-butyllithium, n-propyllithium, isopropyllithium, ethyllithium, cyclohexyllithium, phenyllithium and 2-naphthyllithium, especially n-butyllithium.
  • the anionic initiators are usually used in the process according to the invention in amounts of 0.1 to 15 mmol, preferably 0.2 to 10 mmol, based on 100 g of polymer.
  • alkali metal compounds are also used.
  • the alkali metal compounds can be selected from alkali metal compounds of the following general formulas:
  • R 1 , R 2 , R 3 , R 4 and R 5 are an alkyl group, a cycloalkyl group, an alkenyl group, an aryl group or a partially substituted group thereof having up to 16 C atoms, and
  • M is Na, K, Rb or Cs.
  • alkali metal compounds of the formula R * M are compounds such as methyl sodium, ethyl potassium, n-propyl rubidium, ethyl cesium, t-butyl sodium, t-amyl potassium, n-hexyl rubidium, 4-methyl cyclohexyl sodium, 3-hexenyl potassium, 2,5-decadienyl rubidium, 4,6-di-n-butyldecyl sodium, phenyl potassium, benzyl sodium or 4-tolyl potassium.
  • Alkali metal compounds of the formula R 2 OM which can be used are alkali metal salts of mono- or polyhydric alcohols or phenols, such as the sodium, potassium, rubidium or cesium salts of methyl alcohol, ethyl alcohol, n-propyl alcohol, isopropyl alcohol, t-butyl alcohol, t-amyl alcohol, n-hexyl alcohol, cyclohexyl alcohol,
  • alkali metal compound of the formula R 3 COOM the alkali metal salts of mono- or polyvalent carboxylic acids, such as the sodium, potassium, rubidium or cesium salts of lauric acid, myristic acid, palmitic acid, stearic acid, arachic acid, linoleic acid,. Linolenic acid, phenylacetic acid, benzoic acid, sebacic acid,
  • Phthalic acid or 1,8,16-hexadecantoloyl carboxylic acid can be used.
  • alkali metal compounds of the formula R 4 R 5 NM the alkali metal salts of secondary amines, such as the sodium, potassium, rubidium or cesium salts of dimethylamine, di-n-butylamine, methyl-n-hexylamine, di (3-hexenyl) amine, diphenylamine or dibenzylamine can be used.
  • secondary amines such as the sodium, potassium, rubidium or cesium salts of dimethylamine, di-n-butylamine, methyl-n-hexylamine, di (3-hexenyl) amine, diphenylamine or dibenzylamine can be used.
  • the alkali metal-containing alcohols such as the sodium, potassium, rubidium or cesium salts of methyl alcohol, ethyl alcohol, n-propyl alcohol, isopropyl alcohol, tert-butyl alcohol, tert-amyl alcohol, n-hexyl alcohol, are preferably used in the process according to the invention , Cyclohexyl alcohol, butyl alcohol, phenol or 1-naphthol.
  • the potassium salt of tert-amyl alcohol is very particularly preferably used.
  • the alkali metal compounds are usually used in an amount such that the molar ratio of initiator containing lithium metal or other anionic initiators to alkali metal compounds is about 1: 0.005 to 1: 0.25.
  • modifiers such as ethers and / or aminic compounds, eg tertiary amines, which are able to control the vinyl content in the polymer chain.
  • ether compounds or aromatic compounds particular mention should be made of: triemylamine, pyridine, tetramethylethylene diamine (TMEDA), bis (dimethylaminoethyl) ethane, tetrahydrofuran (THF), diethyl ether, diphenyl ether, anisole, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, ethylene glycol ethyl, tert-butyl ether 2,2-bis (2-oxolanyl) propane or oligomeric oxolanylalkanes.
  • TEZA tetramethylethylene diamine
  • THF tetrahydrofuran
  • diethyl ether diphenyl ether
  • anisole ethylene glycol dimethyl ether
  • ethylene glycol diethyl ether ethylene glycol ethyl
  • the optimal amount of modifiers to be used can easily be determined by appropriate preliminary tests and depends on the desired content of vinyl groups in the polymer chain. Quantities from approx. 0.005 to are usual
  • a preferred embodiment of the process according to the invention can, for example, be designed in such a way that the monomers, for example the conjugated dienes or the conjugated dienes and the vinylaromatic compounds, together with a Ziegler-Natta catalyst or an anionic initiator and the solvent in approximately equal parts in two first reactors connected in parallel are metered in and the polymerization in two further reactors connected in series is completed.
  • the residence time ratio between the first reactors connected in parallel and the subsequent reactors connected in series will be set so that it is in the range of approximately 1.5: 1 and a temperature gradient in the first reactor of ⁇ 10 ° C. is established.
  • the polymerization in the reactors is carried out at temperatures in the range from about 20 to 120 ° C., depending, inter alia, on the catalysts, solvents, reactor types and monomers used. After the end of the polymerization reaction, the polymer obtained is worked up and isolated in a customary and known manner.
  • polybutadienes produced by the process according to the invention using Ziegler-Natta catalysts or catalyst systems contain, depending on
  • Type of the catalysts used a halogen content of less than 400 ppm, preferably 300 ppm, in particular 200 ppm, a content of transition metal ions of less than 250 ppm, preferably 150 ppm, in particular 100 ppm, an ash content of less than 0.15, preferably 0.12, in particular 0.1% by weight and have a content of cis-1,4 bonds in the polymer of> 96%, preferably> 97%, in particular> 98%.
  • polybutadienes When using Ziegler-Natta catalysts or catalyst systems based on titanium, polybutadienes are obtained which have a cis 1,4-content in the polymer of about 92 to 93%.
  • the elastomers produced according to the invention can be vulcanized in a known manner. They can be used for the production of all kinds of rubber articles, preferably for the production of tires or tire components or of golf balls. It is also possible, particularly in the case of polybutadiene, to use this for the production of "high impact polystyrene” (HIPS).
  • HIPS high impact polystyrene
  • the method according to the invention makes it possible to produce elastomers which have an extremely low content of undesired by-products and by-products and thus have an excellent product quality. An additional, complex cleaning of the elastomers obtained can therefore be omitted.
  • the method according to the invention can be regarded as extremely economical. Examples
  • NdBR neodymium polybutadiene
  • the processes described in the individual examples below were carried out in a continuous manner in a plurality of stirred reactors connected in series under adiabatic conditions.
  • the total volume of the reactors was 80 m 3 .
  • the total conversion of butadiene in the polymerization was quantitative.
  • the polymerization was carried out under inert conditions with hexane as the solvent. Both the solvent used and the monomer used (1,3-butadiene) had been dried beforehand and metered into the reactors in this form.
  • the butadiene concentration in the solvent was 18.5%.
  • the reactors, ie the plant were each run with a load of 71 butadiene h. After the end of the polymerization, the polybutadiene obtained was separated from the solvent in a conventional manner, worked up accordingly and dried.
  • the catalyst system used in all examples was neodymium versatate (NdV) in combination with ethyl aluminum sesquichloride (EASC) and diisobutyl aluminum hydride (DIBAH).
  • the amount of catalyst system used or used can be seen from the examples below.
  • the polymerization was carried out at temperatures from 60 to 90 ° C. (first reactor) and 70 to 120 ° C. (remaining reactors). Comparative example
  • the comparative example was carried out in such a way that the residence time of the butadiene used in the first reactor was 1: 3 compared to the residence time of the butadiene used and the polybutadiene formed in the remaining reactors.
  • the temperature gradient in the first reactor was: 11 ° C.
  • the catalyst consumption of neodymium versatate was 0.13 phr, of EASC 0.048 phr and of DIBAH 0.15 phr.
  • a polybutadiene After complete conversion of the 1,3-butadiene used, a polybutadiene was obtained which had a cis 1,4-content of 96%, a metal ion (neodymium) content of 280 ppm, an ash content of 0.16% by weight and a chlorine content of 440 ppm. After a runtime of only 1 month, the reactors had to be switched off and cleaned due to gelling.
  • the polymerization of the butadiene was carried out in an analogous manner to that in the comparative example, with the difference that the residence time ratio was 1: 1 and a temperature gradient of 10 ° C. was set in the first reactor.
  • the consumption of neodymium versatate was 0.05 phr, EASC 0.0185 phr and DIBAH 0.15 phr during the polymerization.
  • a polybutadiene with a cis-1,4 content of 97.5% with a metal ion (Nd) content of 140 ppm and an ash content of 0.11% by weight was obtained.
  • the chlorine content was 220 ppm.
  • the service life of the reactors was 6 months, ie after 6 months the reactors were switched off and cleaned.
  • the polymerization of the butadiene was carried out analogously to the previous examples.
  • the residence time ratio was 1.5: 1.
  • the consumption of neodymium versatate was 0.035 phr, EASC 0.0092 phr and DIBHA 0.14 phr.
  • the service life of the reactors was 12 months.
  • Example 1 In the present comparative example, four reactors were connected in series. In Example 1 according to the invention, two reactors were connected in parallel (first
  • Example 2 Reactor
  • three reactors were connected in parallel, followed by one reactor in series.
  • a total of four reactors were also in use.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Polymerisation Methods In General (AREA)
  • Graft Or Block Polymers (AREA)

Abstract

La présente invention concerne un procédé de production d'élastomères en continu à partir de diènes conjugués ou à partir de diènes conjugués et de composés vinylaromatiques ou à partir d'alcènes, la polymérisation s'effectuant en respectant des temps de séjour donnés des monomères utilisés et des élastomères obtenus dans les réacteurs, tout en respectant des gradients de température donnés dans le premier réacteur. Les élastomères obtenus grâce au procédé de l'invention se caractérise en particulier par une teneur limitée en ions métalliques, une teneur limitée en cendres, et une teneur élevée en liaisons cis-1,4 dans le polymère. De plus, le procédé de l'invention s'avère particulièrement économique.
EP02708315A 2001-02-07 2002-01-25 Procede de production d'elastomeres en continu Withdrawn EP1368391A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE10105401A DE10105401A1 (de) 2001-02-07 2001-02-07 Kontinuierliches Verfahren zur Herstellung von Elastomeren
DE10105401 2001-02-07
PCT/EP2002/000795 WO2002062860A1 (fr) 2001-02-07 2002-01-25 Procede de production d'elastomeres en continu

Publications (1)

Publication Number Publication Date
EP1368391A1 true EP1368391A1 (fr) 2003-12-10

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EP02708315A Withdrawn EP1368391A1 (fr) 2001-02-07 2002-01-25 Procede de production d'elastomeres en continu

Country Status (12)

Country Link
US (1) US6521720B2 (fr)
EP (1) EP1368391A1 (fr)
JP (1) JP4727905B2 (fr)
KR (1) KR20030072620A (fr)
CN (1) CN1229402C (fr)
BR (1) BR0206965B1 (fr)
CA (1) CA2437291C (fr)
DE (1) DE10105401A1 (fr)
HK (1) HK1065053A1 (fr)
MX (1) MXPA03007046A (fr)
TW (1) TWI287023B (fr)
WO (1) WO2002062860A1 (fr)

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JP6751095B2 (ja) 2015-01-28 2020-09-02 株式会社ブリヂストン コールドフロー耐性の向上したシス−１，４−ポリジエン
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KR102213173B1 (ko) * 2017-06-07 2021-02-05 주식회사 엘지화학 연속식 중합에 의한 공액디엔계 중합체의 제조방법
KR102154046B1 (ko) * 2017-10-26 2020-09-09 주식회사 엘지화학 연속식 중합에 의한 공액디엔계 중합체의 제조방법
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See references of WO02062860A1 *

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US6521720B2 (en) 2003-02-18
CN1229402C (zh) 2005-11-30
CN1491241A (zh) 2004-04-21
DE10105401A1 (de) 2002-08-22
CA2437291C (fr) 2009-09-01
JP4727905B2 (ja) 2011-07-20
BR0206965B1 (pt) 2010-12-14
HK1065053A1 (en) 2005-02-08
KR20030072620A (ko) 2003-09-15
MXPA03007046A (es) 2004-05-24
CA2437291A1 (fr) 2002-08-15
WO2002062860A1 (fr) 2002-08-15
BR0206965A (pt) 2004-03-09
TWI287023B (en) 2007-09-21
JP2004522839A (ja) 2004-07-29
US20020107339A1 (en) 2002-08-08

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