EP0490946A1 - Copolymeres alpha olefiniques ayant une etroite repartition des masses moleculaires et une large repartition de la composition - Google Patents

Copolymeres alpha olefiniques ayant une etroite repartition des masses moleculaires et une large repartition de la composition

Info

Publication number
EP0490946A1
EP0490946A1 EP19900913408 EP90913408A EP0490946A1 EP 0490946 A1 EP0490946 A1 EP 0490946A1 EP 19900913408 EP19900913408 EP 19900913408 EP 90913408 A EP90913408 A EP 90913408A EP 0490946 A1 EP0490946 A1 EP 0490946A1
Authority
EP
European Patent Office
Prior art keywords
copolymer
ethylene
weight
polymer
polymerization
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Withdrawn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
EP19900913408
Other languages
German (de)
English (en)
Inventor
Charles Cozewith
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.)
ExxonMobil Chemical Patents Inc
Original Assignee
Exxon Chemical Patents Inc
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 Exxon Chemical Patents Inc filed Critical Exxon Chemical Patents Inc
Publication of EP0490946A1 publication Critical patent/EP0490946A1/fr
Withdrawn legal-status Critical Current

Links

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
    • C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
    • C08F210/18—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers with non-conjugated dienes, e.g. EPT rubbers
    • 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
    • C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers

Definitions

  • This invention is directed toward novel alpha olefin copolymers having a narrow molecular weight distribution (MWD) and a broad compositional distribution (CD), and a process for making same.
  • MWD molecular weight distribution
  • CD compositional distribution
  • Ethylene-propylene copolymers are important commercial products. Two basic types of elastomeric ethylene-propylene copolymers are commercially available. Ethylene-propylene copolymers (EPM) are saturated compounds requiring vulcanization with free radical generators such as organic peroxides. Ethylene-propylene terpolymers (EPDM) contain a small amount of non-conjugated diolefin, such as dicyclopentadiene, 1,4-hexadiene or ethylidene norbornene, which provides sufficient unsaturation to permit vulcanization with sulfur. Such polymers that include at least two monomers, i.e. EPM and EPDM, will hereinafter be collectively referred to as copolymers.
  • EPM Ethylene-propylene copolymers
  • EPDM Ethylene-propylene terpolymers
  • elastomeric copolymers have outstanding resistance to weathering, good heat aging properties and the ability to be compounded with large quantities of fillers and plasticizers resulting in low cost compounds which are particularly useful in automotive and industrial mechanical goods applications.
  • Typical automotive uses are tire sidewalls, inner tubes, radiator and heater hose, vacuum tubing, weather stripping and sponge doorseals and Viscosity Index (V.I.) improvers for lubricating oil compositions.
  • Typical mechanical goods uses are for appliance, industrial and garden hoses, both molded and extruded sponge parts, gaskets and seals and conveyor belt covers. These copolymers also find use in adhesives, appliance parts as in hoses and gaskets, wires and cable and plastics blending.
  • elastomeric EPM and EPDM copolymers find many and varied uses. It is known that the properties of such copolymers which make them useful in a particular application are, in turn, determined by their composition and structure. For example, the ultimate properties of an EPM or EPDM copolymer are determined by such factors as composition, compositional distribution, sequence distribution, molecular weight, and molecular weight distribution (MWD) .
  • EPM and EPDM copolymers are a function of the catalyst system and polymerization process used to produce them.
  • Elastomeric olefin copolymers may be produced at relatively low polymerization temperatures and pressures by means of the so called Ziegler catalysts which comprise a transition metal compound used in combination with a metal alkyl. More specifically, catalyst systems based on a combination of a vanadium compound, an aluminum alkyl or aluminum alkyl halide and, in some cases, a halogen-containing organic compound which serves as a polymerization promoter are known in the art.
  • U.S. Patent 4,540,753 relates to ethylene copolymers with narrow molecular weight distribution (MWD) and a narrow intermolecular composition distribution (Inter-CD).
  • the catalyst system used in this reference comprises a hydrocarbon-soluble vanadium compound having the formula:
  • the catalyst components are premixed in the premixing device and aged for 1-50 seconds.
  • the inlet temperature of the reaction mixture is about -50o to 150oC.
  • Inter-CD defines the compositional variation, in terms of ethylene content, among polymer chains. It is expressed as the minimum deviation (analogous to a standard deviation) in terms of weight percent ethylene from the average ethylene composition for a given copolymer sample needed to include a given weight percent of the total copolymer sample which is obtained by excluding equal weight fractions from both ends of the distribution. The deviation need not be symmetrical. When expressed as a single number for example 15% Inter-CD, it shall mean the larger of the positive or negative deviations.
  • G.B. Patent 902,385 teaches a process of preparing a copolymer of ethylene and higher 1-olefin that is essentially homogeneous as to its composition using a catalyst system based on VOY n and AIR 3 where Y is alkoxide or acetyacetonate group, and n is 2 or 3, and R is a hydrocarbon radical.
  • Y is alkoxide or acetyacetonate group
  • n is 2 or 3
  • R is a hydrocarbon radical.
  • a mixture of carbon tetrachloride and an inert organic liquid solvent or carbon tetrachloride alone is used as the solvent for the copolymerization reaction.
  • Temperature is within the range of from 0°C to 125°C, more preferably from 25°C to 80°C.
  • a molar ratio of Al/V is from 3 to 8.
  • U.S. Patent 3,000,866 teaches ethylene copolymers with about 20% ethylene units by weight and at least 25% alpha-olefin units by weight and about 0.5% to 10% of dicyclopentadiene units by weight.
  • the catalyst system used in this disclosure is made by mixing vanadium tetrachloride or vanadium oxytrichloride with (R) 3 Al or (R) 2 AlX. The polymerization is conducted by contacting ethylene and dicyclopentadiene in a solution of tetrachloro ethylene with the said catalyst system at temperatures between about 20oC to 100°C.
  • the polymerization is carried out in the presence of a halogenated hydrocarbon compound such as chloroform, methylene chloride or a mixture thereof.
  • the polymerization is carried out at temperatures of from -80°C to +125°C.
  • U.S. Patent 3,301,834 relates to a process for the polymerization of ethylene and for the copolymerization of ethylene with other ethy lenically unsaturated hydrocarbons.
  • the catalyst system comprising vanadium compounds (VOCl 3 or VCl 4 ) and organoaluminum compounds is formed in the presence of a halogenated compound such as benzotrichloride.
  • the ratio of halogenated compound to vanadium compound is preferably from 10:1 to 100:1.
  • the molar ratio of V/Al generally is 1:3 to 1:30, but higher ratios up to 1:3000 are disclosed to be operable.
  • the polymerization temperature range is from room temperature to about 150°C.
  • U.S. Patent 3,349,064 also relates the same catalyst system as that defined in U.S. Patent 3,301,834 except that the halogenated promoter is a group of unsaturated carboxylic compounds containing at least 4 halogen atoms, at least 2 of which are attached to doubly bonded carbon atoms and at least l of which is attached to a singly bonded carbon atom alpha to the double bond (e.g., 2, 2, 3, 4, 5, 5-hexachlorocyclopentene).
  • the use of VCl 4 , TEA and hexachlorocylocpentadiene is described in example 6.
  • the molar ratio of promoter to vanadium compound is preferably from 10:1 to 100:1.
  • U.S. Patent 3,489,729 relates to a method of making EPDM polymer by using the catalyst system comprising R 3 Al organo-aluminum compounds and vanadium compounds having formula VOY n , together with halogen-containing compounds such as hydrogen chloride, elemental chlorine, benzyl chloride, or t-butyl chloride.
  • the temperature for the polymerization is -100 to 200°F.
  • the molar ratio of organoaluminum compound to vanadium compound is in the range of 3/1 to 20/1.
  • the amount of active halogen-containing compound based on vanadium compound is 1 to 30 mols per mol of vanadium compound.
  • BE Patent 592,247 teaches a process for preparing copolymer of ethylene with alpha-olefins whose molecular weight depends on the amount of halogenated alkanes used.
  • Triisobutyl aluminum ([(CH 3 ) 2 CH 2 ] 3 AI) , vanadium tetrachloride (VCl 4 ) and carbon tetrachloride (CCl 4 ) may be used as a catalyst system.
  • GB Patent 1,059,865 relates to the polymerization of ethylene, or ethylene together with one or more olefin monomers.
  • TEA, CCl 4 , CHCl 3 , and vanadium di-isopropyl salicylate are used as the catalyst system.
  • the breadth of the intermolecular compositional distribution (CD) and molecular weight distribution (MWD) of polymers such as prepared by the above referenced disclosures are largely a function of the particular catalyst system employed to prepare the polymer.
  • Such catalyst systems generally yield polymers with either narrow CD and narrow MWD or broad CD and broad MWD.
  • ethylene copolymers (EPM or EPDM) having a broad CD and at the same time a narrow MWD are not believed to have been disclosed in the art.
  • EPM or EPDM ethylene copolymers
  • Such elastomers are especially useful in that they possess novel combinations of properties such as excellent green strength and processability which leads to superior performance in a number of applications.
  • the present invention is directed toward novel elastomeric copolymers of ethylene and at least one other alpha-olefin monomer which copolymers have an intermolecular compositional distribution (CD), as hereinafter defined, such that at least about 25% by weight of the polymer differs from the mean ethylene content of the polymer by at least plus or minus 5 wt % ethylene, and have a relatively narrow molecular weight distribution (MWD) such that the weight average molecular weight (Mw) of the polymer divided by the number average molecular weight (Mn) of the polymer is not greater than about 5.0.
  • CD intermolecular compositional distribution
  • copolymers of this invention which are characterized by exceptional green strength and good processing properties, may be prepared using a catalyst system comprising: a) a vanadium compound with a valence of 3 or more; b) a triorgano aluminum compound; and
  • the catalyst system allows for efficient polymerization of high quality polymer products and at generally higher polymerization temperatures of up to about 140°C to yield higher molecular weight polymer products which are essentially free of gel, and which possess excellent green strength and processability.
  • intermolecular compositional distribution defines the compositional variation among polymer chains in terms of ethylene content as compared with the mean ethylene content of the copolymer as a whole.
  • the CD is expressed by first determining the mean ethylene content of the copolymer sample by a suitable test such as described in ASTM D-3900. Next, the copolymer sample is dissolved in solvent such as hexane and a number of fractions of differing composition are precipitated by the addition of incremental amounts of a liquid such as isopropanol in which the copolymer is insoluble. Generally, from about 4-6 fractions are precipitated in this way and the weight and ethylene content of each fraction are determined after removing the solvent.
  • the mean composition of the copolymer as a whole is 50 weight percent ethylene, D o is about 41 cumulative %, B o is about 56 cumulative %, and B o minus D o is therefore about 15%.
  • about 85% of the copolymer has an ethylene content which is greater by plus or minus 5% than the mean ethylene content of 50% of the copolymer as a whole. This exemplifies a broad compositional distribution within the scope of this invention.
  • MWD Molecular weight distribution
  • Mw/Mn Molecular weight distribution
  • MWD can be measured by gel permeation chromotography (GPC), for instance, using a Waters 150 gel permeation chromatograph equipped with a Chromatix KM-6 on-line light scattering photometer. The system is used at 135°C with 1,2,4 trichlorobenzene as mobile phase. Showdex (Showa-Denko America, Inc.) polystyrene gel columns 802, 803 804 and 805 are used.
  • the elastomeric polymer of this invention comprises ethylene-containing elastomeric polymers that have been copolymerized with one or more higher alpha olefins and optionally a diene monomer.
  • the terms "elastomeric” or “elastomer” are defined to mean that when they are crosslinked, they are capable of recovering from large deformations quickly and forcibly. Free from diluents, the crosslinked polymers retract within one minute to less than 1.5 times their original lengths after being stretched at 18°C-29°C to twice their lengths and held for one minute before release.
  • elastomers are "substantially amorphous", and when that term is used to define the ethylene containing elastomeric polymers of this invention, it is to be taken to mean having a degree of crystallinity less than 25%, preferably less than about 15%, and more preferably less than about 10% as measured by means known in the art.
  • the three major known methods of determining crystallinity are based on specific volume, x-ray diffraction, and infrared spectroscopy.
  • Another well-established method, based on measurement of heat content as a function of temperature through the fusion range, is differential scanning calorimetry. It is known that these independent techniques lead to good experimental agreement.
  • the tendency of a particular combination of catalyst system and monomers to produce blocky, random, or alternating monomer sequence distribution in the polymer can be characterized by the product of the reactivity ratios defined for the given monomers under the specific reaction conditions encountered. If this product is equal to 1.0, the sequence distribution will be perfectly random; the more the product is less than 1.0, the more the monomers will approach alternating sequence; and, the more the product is greater than 1.0, the more the monomers will tend to have a blocky sequence distribution.
  • the segments of a polymer which crystallize are linear segments which have a number of identical (both by chemical make-up and stereo-specific orientation) units in a row. A combination of such segments are said to yield blocky polymer.
  • the ethylene-containing elastomeric polymers of this invention accordingly, have a reactivity ratio product less than 2.0, preferably less than about 1.5, and more preferably less than about 1.25, and are substantially amorphous.
  • copolymers in accordance with the present invention are comprised of ethylene and at least one other copolymerizable alpha-olefin.
  • alpha-olefins include those containing 3 to 18 carbon atoms, e.g., propylene, butene-1, pentene-1, hexene-1, etc.
  • Alpha-olefins of 3 to 6 carbons are preferred due to economic considerations, and they are generally present in the copolymer within the range of about 10 to 90 percent by weight, more preferably from about 15 to about 70 percent by weight most preferably 20 to about 70 percent by weight.
  • the most preferred copolymers in accordance with the present invention are those comprised of ethylene and propylene or ethylene, propylene and a diene.
  • copolymers of ethylene and higher alpha-olefins such as propylene often include other copolymerizable monomers.
  • Typical of these other monomers may be non-conjugated dienes such as the following non-limiting examples: a straight chain acyclic dienes such as
  • d multi-ring alicyclic fused and bridged ring dienes such as: tetrahydroindene ; methyltetrahydroindene; dicyclopentadiene; bicyclo-(2,2,1)-hepta2,5-diene; alkenyl, alkylidene, cycloalkenyl and cycloalkylidene norbornenes such as 5-methylene-2-norbornene (MNB) , 5-ethylidene-2-norbornene (ENB) , 5-propyl-2-norbornene,
  • dienes containing at least one of the double bonds in a strained ring are preferred.
  • the most preferred diene is 5-ethylidene-2-norbornene (ENB).
  • ENB 5-ethylidene-2-norbornene
  • the amount of diene (wt. basis) in the the copolymer may be from about 0% to 20% with 0% to 15% being preferred. The most preferred range is 0% to 10%. Where the diene is present, it is generally present at a minimum level of about 1 weight percent.
  • the most preferred copolymer in accordance with the present invention is ethylene-propylene or ethylene-propylene-diene.
  • the average ethylene content of the copolymer may be as low as about 10% on a weight basis.
  • the preferred minimum is about 25%.
  • a more preferred minimum is about 30%.
  • the maximum ethylene content may be about 90% on a weight basis.
  • the preferred maximum is about 85%, with the most preferred being about 80%.
  • a further unexpected characteristic of the copolymer of this invention is the broad compositional distribution of the optionally included non-conjugated diene.
  • copolymer having typically narrow MWD will also be expected to have a narrow compositional distribution of non-conjugated diene.
  • the copolymer of this invention containing non-conjugated diene will thus exhibit a compositional distribution such that the diene content of at least about plus or minus 20% of the polymer differs from the mean value of incorporated non-conjugated diene by at least plus or minus 0.5 weight percent diene.
  • a typical curve representing this compositional distribution appears in the upper portion of Figure 1.
  • the molecular weight of copolymer made in accordance with the present invention can vary over a wide range.
  • the preferred minimum is about 10,000.
  • the most preferred minimum is about 20,000.
  • the maximum weight average molecular weight may be as high as about 12,000,000.
  • the preferred maximum is about 1,000,000, with the most preferred maximum being about 750,000.
  • Copolymers prepared in accordance with the present invention exhibit a broad CD with at least about 25% of the polymer differing from the mean ethylene content by ⁇ 5% ethylene, and a relatively narrow molecular weight distribution within the range of from about 2 to 5, evaluated as described above.
  • Copolymers having the most superior green strength and processing properties are those having a CD breadth ranging from about 40% to about 80% of the polymer differing from the mean ethylene content by ⁇ 5% and (M w /M n ) of from greater than about 2.0 up to about 4.5.
  • novel copolymers of this invention are produced using a catalyst system comprising: a) a hydrocarbon soluble, non-supported vanadium
  • the vanadium component of the catalyst system may have the general formulas
  • X is halogen, preferably chlorine
  • Y is an organic substituent selected from the group consisting of an alcoholate, carboxylate, ketonate or diketonate having up to 10 carbon atoms
  • a and b may range from 0 to 3 with the proviso that the sum of a and b is 2 or 3
  • c and d may range from 0 to 4 with the proviso that the sum of c and d is 3 or 4.
  • Preferred vanadium compounds for the purposes of this invention include:
  • R is a hydrocarbon radical preferably having from about 1 to 10 carbon atoms.
  • R preferably represents an aliphatic, alicyclic or aromatic hydrocarbon radical such as ethyl (Et), phenyl, isopropyl, butyl (Bu), propyl, n-butyl, i-butyl, t-butyl, hexyl, cyclohexyl, octyl, naphthyl and so forth.
  • Non limiting and illustrative examples of preferred vanadium compounds are vanadyl tetrahalides and trihalides, alkoxy halides and alkoxides, such as VCl 4 , VOCl 3 , VOCl 2 (OEt) , VOCl 2 (OBu) , VO(OBu) 3 and VO(OC 2 H 5 ) 3 .
  • the most preferred vanadium compounds are the chlorinated compounds such as VOCl 3 , VCl 4 and VOCl 2 (OR).
  • the triorgano aluminum component of the catalyst system has the formula AlR 3 wherein R is a hydrocarbon radical having one to ten carbon atoms as defined above with respect to he vanadium compounds.
  • R is a hydrocarbon radical having one to ten carbon atoms as defined above with respect to he vanadium compounds.
  • suitable R groups include methyl, ethyl, i-butyl, hexyl and phenyl.
  • Preferred compounds are trialkyl aluminum compounds, including triethyl, tri isobutyl and tri n-hexyl aluminum. It is important for the purposes of this invention that the aluminum compound is free of halogen, i.e., that aluminum alkyl halides not be used. Catalytic activity is markedly reduced using these latter compounds.
  • halogenated polymerization promoter is a key feature of the present invention.
  • a certain range of halogen substituent reactivity toward the catalyst is required to give the proper balance of catalyst activity and properties of the copolymer product. If the reactivity is too low, catalyst efficiency is reduced, while if it is too high, undesirable side reactions occur which are deleterious to catalyst performance.
  • Cooper T.A Cooper, Journ. Am. Chem. Soc., 95, 4158 (1973), the disclosure of which is incorporated herein by reference, has defined in Table 1 an organic halide activity index based on the ability of the halide to oxidize VCl 2 (py) 4 to V(III) under standard conditions. For example, CCl 4 is assigned a reactivity of 1 in tetrahydrofuran at 20°C, and other listed halogenated organic compounds have reactivities of from about 0.02 to greater than 200 relative to CCl 4 .
  • organic halides as defined in the above referenced article with a Cooper Index ranging from about 0.01 up to about 30 are suitable promoters for the purposes of this invention.
  • Most preferred promoters meeting this criteria are selected from the group consisting of carbon tetrachloride, hexachloroethylene, benzyl bromide, benzyl chloride and 2,3-or 1,3-dichloropropylene.
  • vanadium component of the catalyst system is both not hydrocarbon insoluble and not supported on an inert or hydrocarbon insoluble support. Vanadium Catalyst systems that are hydrocarbon insoluble or deposited on inert supports are not typically useful for the preparation of elastomeric copolymers of ethylene according to the procedures of this invention.
  • the polymerization in accordance with this invention may be carried out either in solution or in suspension, but solution polymerization is preferred to avoid problems of reactor fouling.
  • the process may be carried out as a batch process or a continuous process, although continuous flow stirred tank reactors are preferred, and at normal atmospheric pressure or under elevated or reduced pressures.
  • the polymerization may also be carried out using a series of two or more continuous flow stirred tank reactors or equivalents thereof. Normally, pressures of 1-10 atmospheres are preferred.
  • the polymerization may be carried out at temperatures in the range of about 60 to about 140°C, as well as the more common temperatures within the range of about 10 to 60°C.
  • Preferred polymerization temperatures for the purposes of this invention lie in the range of from about 40 to 120oC, more preferably from about 55 to 100°C.
  • Solvents used in the process include one or a mixture of hydrocarbons such as pentane, hexane, benzene, toluene, xylene, cyclo hexane and the like.
  • Diluents useful for a suspension process are propane, butane or a mixture of the liquefied monomers useful in accordance with this invention.
  • the solvent will also be a solvent for the vanadium catalyst compound.
  • the polymerization reaction should be conducted in the absence of oxygen, carbon dioxide, water and other materials which have a deleterious effect on the catalyst activity.
  • the catalyst and halogenated promoter may be combined prior to contact with the monomers, or dilute solutions of these components may be introduced separately into the reactor. It is preferred for the purposes of this invention that the vanadium catalyst and alkyl aluminum are introduced separately into the reactor and allowed to react to form the active catalyst in the presence of the monomers, since catalyst activity may suffer if the catalyst components are premixed. Also, it is preferable not to premix the promoter and alkyl aluminum since undesirable side reactions might occur.
  • Polymer molecular weight may be controlled by the introduction of known chain transfer agents such as hydrogen gas or diethyl zinc.
  • chain transfer agent such as hydrogen gas or diethyl zinc.
  • the quantity of chain transfer agent introduced into the reactor ranges from about 0.1 to about 100 moles per mole of vanadium catalyst.
  • chain branching suppressors including Lewis Bases such as NH 3 , pyridine and Si(OEt) 4 to the reactor along with the catalyst components.
  • the preferred molar ratio of such suppressors ranges from about 1:2 to 10:1 with respect to the quantity of the vanadium catalyst employed.
  • the average residence time of the reactants in the reactor generally ranges from about 5 minutes to about 2 hours or more.
  • the polymer product can be conventionally recovered from the effluent by coagulation with a nonsolvent such as isopropyl alcohol or n-butyl alcohol, acetone, or the polymer can be recovered by stripping the solvent with heat or steam.
  • a nonsolvent such as isopropyl alcohol or n-butyl alcohol, acetone
  • An antioxidant can be incorporated in the polymer during the recovery procedure, such as phenyl-beta-naphthylamine; di-tert-butylhydroquinone, triphenyl phosphite, heptylated diphenylamine,
  • the amount of the vanadium catalyst employed in the present invention is relatively low as compared with prior art processes not employing a promoter.
  • the amount of vanadium catalyst ranges from about 0.02 to about 0.5 millimoles per liter of solvent solution, with levels of from about 0.05 to about 0.5 millimoles being most preferred.
  • the molar amounts of vanadium catalyst and aluminum compound added to the reaction medium should provide a molar ratio of aluminum to vanadium (Al/V) of at least about 10 and not greater than about 250. Preferred such ratios range from about 15 to 50.
  • the amount of halogenated organic promoter used with respect to the vanadium compound may generally range in the promoter/V molar ratio of between about 5 to about 250. It is desirable that the promoter/V ratio be not substantially higher than the Al/V ratio, and preferred ratios range from about 5 to about 50.
  • Catalyst, cocatalyst, promoter, and diene monomer were prepared as dilute solutions in hexane and each was pumped separately into the reactor via metering pumps. H 2 was also added to the reactor to control polymer molecular weight, and in some cases NH 3 was added to suppress any tendency for long chain branching. Temperature in the reactor was controlled by circulating water through a jacket. Iso-propyl alcohol was added to the polymer solution exiting the reactor to terminate polymerization, and the solution was added to boiling water to remove solvent and monomers. The wet polymer was then dried on a hot rubber mill to yield the final product. Polymerization rate was measured by determining the weight of polymer produced in a fixed period of time.
  • Polymer ethylene content was determined by ASTM D3900. Ethylidene norbornene content was measured by infrared based on the height of the 1690 cm -1 band. Mooney viscosity was determined by ASTM D1646. The compositional distribution (CD) and molecular weight distribution (MWD) of the polymer were determined as described above.
  • the CD was determined by cutting a sample of the finished copolymer into small pieces and adding the pieces to hexane to give a concentration of about lg/lOOcc. This mixture was then stirred gently at 22°C for 48 hours, or until equilibrium is reached. The mixture is then poured through a fine mesh stainless steel screen to recover any insoluble polymer, which is dried, weighed and analyzed for composition. Isopropanol is then slowly added to the solution until precipitated polymer first appears. This polymer is recovered on a screen, dried, weighed and also analyzed for composition. Additional isopropanol is added incrementally to the remaining solution to precipitate four to six fractions in total, all of which are recovered as described previously.
  • the final isopropanol-hexane solution is then evaporated to dryness to yield a final polymer fraction.
  • a plot is prepared of weight percent composition vs cumulative weight percent polymer as described above and as illustrated in Figure 1.
  • a polymerization was conducted by the process described above with a VCl 4 -triethyl aluminum (TEA) catalyst system with CCl 4 as a promoter at a temperature of 75°C .
  • NH 3 was also added to the reactor at a NH 3 /V molar ratio of 1: 1.
  • Hexane feed rate was 2500 g/hr. All other polymerization conditions are given in Table 1. The polymerization went smoothly giving high monomer conversion and high catalyst activity.
  • Polymer fractionation by the process described above gave the cumulative composition curve shown in Figure 1.
  • Polymer species were present that ranged from at least 65.5 wt% ethylene to at least 35.5 wt% ethylene. From this figure it can be determined that about 44% the polymer had an ethylene content 5% higher than the mean of 50%, while about 41% of the polymer had an ethylene content 5% less than the mean. Thus, the CD of this polymer is 85%. Mw/Mn for this polymer was 3.0.
  • This example illustrates the use of the VOCl 3 /TEA catalyst system with CCl 4 promoter at a polymerization temperature of 75oC.
  • NH 3 was added to the reactor at NH 3 /V molar ratio of 1:1.
  • Hexane flow rate was 2500 g/hr.
  • catalyst activity was high and monomer conversions were good.
  • About 65% of the polymer has an ethylene content ⁇ 5% greater than the mean value.
  • Mw/Mn for this polymer was 3.8.
  • This run illustrates the use of benzyl chloride as a promoter with the VCl 4 /TEA catalyst system.
  • Benzyl chloride has a Cooper reactivity index of .05.
  • An NH 3 /V molar ratio of 1:1 was used and the hexane flow rate was 2500 g/hr.
  • the composition distribution of the polymer was such that 64 wt% of the polymer has an ethylene content ⁇ 5% greater than the mean value.
  • Mw/Mn for the polymer is 3.1.
  • This example illustrates the use of various promoters with the VOCl 3 /TEA catalyst system at 75°C polymerization temperature.
  • the hexane feed rate was 2500 g/hr and the other polymerization conditions are as shown in Table 1.
  • the promoters used are indicated below:
  • Benzoyl chloride has a Cooper Index of 40. Large amounts of insoluble polymer were produced and steady-state operating data could not be obtained.
  • trichlorotoluene was used as a promoter with the VOCI 3 -TEA catalyst system.
  • Trichlorotoluene has a Cooper Index of 40.
  • Polymerization conditions and results are shown in Table 1. Hexane feed rate was 2500 g/hr. In the copolymerization runs, 7A and 7B, catalyst activity was very high. GPC analysis of the copolymer produced in run 7B indicated a broad, bimodal MWD, with a low MW mode shifted to a Mn of 251 and a high MW mode with an Mn of 31,000. Mw/Mn for polymer 7B was 80.
  • Vanadium tris-hexanoate was prepared by reacting VCl 3 with hexanoic acid. A terpolymerization was carried out with this catalyst and TEA cocatalyst with CCl 4 as the promoter. Polymerization results are shown in Table 2. Hexane feed rate was 3030 g/hr and a NH 3 /V ratio of 0.65 was used. The compositional distribution was broad with 77% of the polymer greater than ⁇ 5 wt% ethylene from the mean. Mw/Mn was 4.3.
  • Vanadium chloride bis hexanoate was prepared by the reaction of VCl 3 with 2 moles of hexanoic acid . A polymerization was carried out with this catalyst and TEA cocatalyst with CCl 4 as the promoter. As shown by the results in Table 2 , catalyst activity was good. The polymer had an Mw/Mn of 4 . 0 and 72% of the polymer differed from the mean composition by greater than ⁇ 5 wt% ethylene.
  • Example 15 The polymerization procedure described in Example 15 was used except that the polymerization was carried out in two 7.6 liter volume stirred tank reactors connected in series. Catalyst, solvent and monomers were fed to the first reactor, and the product stream entered the second reactor to which additional monomers dissolved in hexane solvent were added. Polymerization conditions are given in Table 3.
  • the catalyst system was VCl 4 /TEA with CCL 4 as promoter. Hexane feed to the two reactors was 29.9 and 4.45 kg/hr respectively. Runs A and B are essentially similar except that additional ethylene was fed to the second reactor in Example 16B.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

L'invention concerne de nouveaux copolymères d'éthylène et au moins un nouveau alpha oléfinique. Lesdits copolymères ont une répartition intermoléculaire de la composition (CD) telle qu'au moins environ 25 % en poids du polymère soit différent du contenu moyen en éthylène du polymère par au moins environ 5 % en poids d'éthylène, ainsi qu'une distribution des masses moléculaires (MWD) relativement étroite afin que la masse moléculaire (Mw) moyenne en poids du polymère divisée par la masse moléculaire (Mn) moyenne en nombre ne soit pas supérieur à environ 5,0. Ces polymères , caractérisés par une résistance en vert exceptionnelle et par de bonnes propriétés de transformation, peuvent ètre préparés au moyen d'un système catalyseur qui comprend: a) un composé de vanadium dont la valence est d'au moins 3; b) un composé de triorganoaluminium; et c) un promoteur organique halogéné et spécifique utilisé en quantités catalytiques. Le système catalyseur permet une polymérisation efficace des produits polymères de haute qualité à des températures de polymérisation généralement plus élevées allant jusqu'à environ 140 °C afin de donner des produits polymères à masse moléculaire plus élevée qui sont essentiellement dépourvus de gels et qui possèdent une résistance en vert et une transformabilité excellentes.
EP19900913408 1989-09-06 1990-09-04 Copolymeres alpha olefiniques ayant une etroite repartition des masses moleculaires et une large repartition de la composition Withdrawn EP0490946A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US40395389A 1989-09-06 1989-09-06
US403953 1989-09-06

Publications (1)

Publication Number Publication Date
EP0490946A1 true EP0490946A1 (fr) 1992-06-24

Family

ID=23597548

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19900913408 Withdrawn EP0490946A1 (fr) 1989-09-06 1990-09-04 Copolymeres alpha olefiniques ayant une etroite repartition des masses moleculaires et une large repartition de la composition

Country Status (5)

Country Link
EP (1) EP0490946A1 (fr)
JP (1) JPH05500080A (fr)
AU (1) AU6337690A (fr)
CA (1) CA2065302A1 (fr)
WO (1) WO1991003505A1 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL9400758A (nl) * 1994-05-06 1995-12-01 Dsm Nv Werkwijze voor de bereiding van een hoogmoleculair polymeer uit etheen, alfa-olefine en eventueel dieen.
US8497330B2 (en) 1997-12-08 2013-07-30 Univation Technologies, Llc Methods for polymerization using spray dried and slurried catalyst
US6242545B1 (en) 1997-12-08 2001-06-05 Univation Technologies Polymerization catalyst systems comprising substituted hafinocenes
IT1302259B1 (it) * 1998-09-24 2000-09-05 Enichem Spa Procedimento per la preparazione di copolimeri ep(d) m a ristrettadistruzione dei pesi molecolari.

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB902385A (en) * 1959-10-14 1962-08-01 Hercules Powder Co Ltd Improvements in or relating to copolymerization process
US3349064A (en) * 1962-09-28 1967-10-24 Hercules Inc Polymerization and copolymerization of ethylene using halogen-containing promoters
GB1059865A (en) * 1964-07-30 1967-02-22 Shell Int Research Ethylene polymerisation and copolymerisation
US4540753A (en) * 1983-06-15 1985-09-10 Exxon Research & Engineering Co. Narrow MWD alpha-olefin copolymers
US4786697A (en) * 1983-06-15 1988-11-22 Exxon Research & Engineering Co. Molecular weight distribution modification in a tubular reactor
JPH0696655B2 (ja) * 1985-08-02 1994-11-30 エクソン・ケミカル・パテンツ・インク 加工性の良いエチレンプロピレンエラストマー

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9103505A1 *

Also Published As

Publication number Publication date
CA2065302A1 (fr) 1991-03-07
JPH05500080A (ja) 1993-01-14
AU6337690A (en) 1991-04-08
WO1991003505A1 (fr) 1991-03-21

Similar Documents

Publication Publication Date Title
US4789714A (en) Molecular weight distribution modification in tubular reactor
US4786697A (en) Molecular weight distribution modification in a tubular reactor
US4882406A (en) Nodular copolymers formed of alpha-olefin copolymers coupled by non-conjugated dienes
US4016342A (en) Process and product
US4716207A (en) Nodular copolymers comprising narrow MWD alpha-olefin copolymers coupled by non-conjugated dienes
US4540753A (en) Narrow MWD alpha-olefin copolymers
EP1113028B1 (fr) Procédé pour la préparation de polymères d'oléfines ayant des ramifications à longues chaînes
US5191042A (en) Process for preparing alpha-olefin copolymers having a narrow MWD and broad compositional distribution
US4959436A (en) Narrow MWD alpha-olefin copolymers
US6465584B1 (en) Elastomeric copolymer and process for the preparation thereof
EP0059034B1 (fr) Procédé de production de copolymères d'éthylène avec des alpha-oléfines
US5013801A (en) Molecular weight distribution modification in a tubular reactor
JP4033950B2 (ja) 残留塩素含有量が低いエチレンプロピレン共重合体の製造法
EP0490946A1 (fr) Copolymeres alpha olefiniques ayant une etroite repartition des masses moleculaires et une large repartition de la composition
EP1339788B1 (fr) Composition polymere, processus de preparation de cette composition et elements moules de cette composition
US4031300A (en) High molecular weight, high unsaturation isobutylene-cyclopentadiene copolymers
AU585938B2 (en) Olefin copolymers coupled by dienes
US4978720A (en) Olefinic chlorosilane and olefinic halide functional group containing polymers and method of forming the same
AU579446B2 (en) Molecular weight distribution modification
EP0235381B1 (fr) Copolymères caoutchouteux d'éthylène-alpha-oléfines
EP0792296B1 (fr) Procede pour la preparation d'un copolymere semblable a du caoutchouc
AU599627B2 (en) Copolymers of olefinic chlorosilanes and/or halides
US9574033B1 (en) Process for continuously making high molecular weight tetrapolymer for use in anti-vibration applications
US3845159A (en) Tetrapolymer of ethylene/c3-c12 alpha-monoolefin/maleic anhydride/c6-c22 nonconjugated diene
EP0202060B1 (fr) Utilisation d'un silicate pour réprimer la ramification de chaînes pendant la préparation de caoutchouc EPDM

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19920323

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): BE DE ES FR GB IT NL

17Q First examination report despatched

Effective date: 19931228

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 19960131