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    • 专利摘要:
    SUMMARY PROCESS FOR PREPARING A MULTIMETHAL PRO-CATALYST, PRO-CATALYST, POLYMERIZING CATALYST, POLYETHYLENE POLYMER, COMPOSITION AND ARTICLE New catalyst compositions, comprising three or more transition metals, are effective in increasing catalytic efficiency, reducing polydispersity, and increase the uniformity of molecular weight distribution when used in olefin and, particularly, polymerizations of linear low density polyethylene (LLDPE). The resulting polymers can be used to form differentiated products including, for example, films that can exhibit improved optical and mechanical properties.
    公开号:BR112013030650B1
    申请号:R112013030650-5
    申请日:2012-05-23
    公开日:2020-06-23
    发明作者:Sylvie Desjardins；Mehmet Demirors；Ellen Donkers；Philip P. Fontaine；Philip P Fontaine；Cristina Serrat
    申请人:Dow Global Technologies Llc；
    IPC主号:
    专利说明:

    History of the Invention Field of the Invention
    The invention relates to Ziegler-Natta catalysts useful for olefin polymerizations. More particularly, it refers to multimetal Ziegler-Natta catalysts, showing efficiency and improved properties in the production of ethylene-based polymers, such as linear low density polyethylene (LLDPE) polymers in particular. Technique History
    Currently, the demand for polyethylene worldwide exceeds the mark of 80 million metric tons per year. Because there is a need for a continuous and significant differentiation of polymeric products in the polyethylene sector, researchers make a lot of efforts to seek changes in the process to produce these new products. One focus involves exploring new catalysts.
    Ziegler-Natta catalysts have been used for many years in the production of a variety of polyethylene, including LLDPE. These catalysts generally include a magnesium halide support and one or two transition metal compounds. Although efficient, these catalysts often result in LLDPE resins with wide polydispersity and undesirably wide short chain branch (SCBD) distribution.
    In the production of LLDPE, ethylene is generally copolymerized with a short chain olefin comonomer (for example, 1-butene, 1-hexene, 1-octene). The resulting polymer is substantially linear, but includes significant numbers of short branches, and these characteristics confer higher tensile strength, greater impact resistance and greater puncture resistance than those of low density polyethylene (LDPE). These improved properties, in turn, mean that thinner (gauge) films can be blown and the product exhibits crack resistance under improved environmental stress. LLDPE is used predominantly in film applications due to its toughness, flexibility and relative transparency. Product examples range from agricultural films, food protection films and bubble wrap to multilayer and composite films. Unfortunately, LLDPE tends to be more difficult to process than LDPE and can also be less tenacious and / or exhibit some less desirable optical properties.
    In view of the above-mentioned deficits in the performance of many known LLDPE polymers, it is desirable to identify process and / or compositional means and methods that can be employed in the production of new and differentiated LLDPE polymers. In addition, it is desirable that these new media and / or methods offer advances in the process and product such as improved catalytic efficiencies, narrower polydispersities, as well as narrower SCBD to achieve improved uniformity of these products. Summary of the Invention
    In a first embodiment, the present invention provides a process for preparing a pro-catalyst comprising (a) reacting a hydrocarbon-soluble organomagnesium compound or its complex, and an active metal or non-metallic halide to form a halogenated magnesium support; (b) contacting the magnesium halide support with a conditioning compound containing an element selected from the group consisting of boron, aluminum, gallium, indium and tellurium, under conditions sufficient to form a conditioned magnesium halide support; (c) contacting the conditioned magnesium halide support and a compound containing, as the first metal, titanium, to form a supported titanium compound; (d) contacting the supported titanium compound and a second metal and a third metal, independently selected from the group consisting of zirconium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum, and tungsten, provided that the second metal and the third metal don't be the same; and as long as the molar ratio of magnesium to a combination of titanium and the second and third metals varies from 30: 1 to 5: 1, under conditions sufficient to form a multimetal pro-catalyst.
    In a second embodiment, the present invention provides a multimetal pro-catalyst obtained according to the process described above in the first embodiment.
    In a third embodiment, the present invention provides a multimetal polymerization catalyst comprising the reaction product of the multimetal pro-catalyst, as described above, and an organometallic cocatalyst.
    In a fourth embodiment, the present invention provides a polyethylene polymer prepared by a process in which ethylene and optionally one or more olefinic comonomers are polymerized in the presence of the trimetallic polymerization catalyst, as described above.
    In yet another aspect, the invention provides an LLDPE polymer with a polydispersity of less than 3.50, optionally a high density fraction of less than 25 weight percent and a molecular weight at a comonomer content ratio (MWCCR) in the range from 0.75 to 1.1.
    In yet another aspect, the invention provides an LLDPE polymer prepared through a process in which the pro-catalyst composition described above is contacted with an organometallic cocatalyst, so that a catalyst is formed; and an olefinic comonomer under conditions such as to form an LLDPE polymer with the properties mentioned above.
    In yet another aspect, the invention provides an article prepared with this LLDPE polymer. Detailed Description of Achievements
    The catalyst compositions of the invention can be defined here as at least trimetallic, but they can also include more than three transition metals, and can thus be defined in a more comprehensive embodiment as multimetallic. These three or more transition metals are specifically selected before the catalyst is produced. Although a wide variety of combinations are possible, all catalysts used in the invention include titanium as an element.
    The catalyst compositions can be prepared by starting first with the preparation of a conditioned magnesium halide support. The preparation of a conditioned magnesium halide support begins with the selection of an organomagnesium compound or complex, including an organomagnesium compound. This compound or complex is desirably soluble in an inert hydrocarbon diluent. The concentrations of components are preferably such that when the active halide, such as a metallic or non-metallic halide, and the magnesium complex are combined, the resulting slurry is from about 0.005 to about 0.2 molar (moles / liter) in relation to magnesium. Examples of suitable inert organic diluents include liquefied ethane, propane, isobutane, n-butane, n-hexane, the various isomeric hexanes, isooctane, paraffinic mixtures of alkanes having 5 to 10 carbon atoms, cyclohexane, methylcyclopentane, dimethylcyclohexane, dodecane, industrial solvents composed of saturated or aromatic hydrocarbons, such as kerose, naphtha, and combinations thereof, especially when free of any olefinic compounds and other impurities, and especially those with boiling points in the range of about -50 ° C to about 200 ° C. Also included, as appropriate inert diluents, are ethylbenzene, cumene, decaline and combinations thereof.
    Suitable organomagnesium compounds and complexes may include, for example, C2-C8 magnesium alkyl and aryl, magnesium alkoxides and aryloxides, carboxylated magnesium alkoxides, and carboxylated magnesium aryloxides. Preferred sources of magnesium moieties can include C2-C8 alkyl magnesium and C1-C4 alkoxides. That organomagnesium compound or complex can be reacted with a metal or non-metal halide source, such as chloride, bromide, iodide or fluoride, to prepare a magnesium halide compound under appropriate conditions. Such conditions can include a temperature ranging from -25 ° C to 100 ° C, preferably from 0 ° C to 50 ° C; a time ranging from 1 to 12 hours, preferably from 4 to 6 hours; or both. The result is a magnesium halide based support.
    The magnesium halide support is then reacted with an appropriate conditioning compound containing an element selected from the group consisting of boron, gallium, indium and tellurium, under conditions suitable to form a conditioned magnesium halide support. That compound and the magnesium halide support are then brought into contact under sufficient conditions to result in a conditioned magnesium halide support. Such conditions may include a temperature ranging from 0 ° C to 50 ° C, preferably from 25 ° C to 35 ° C; a time ranging from 4 to 24 hours, preferably from 6 to 12 hours; or both. Without being linked to any mechanism theory, it is suggested that this aging serves to facilitate or increase the adsorption of additional metals on the support.
    After the conditioned support is prepared and properly aged, it is placed in contact with a titanium compound. In certain preferred embodiments, titanium halides or alkoxides, or combinations thereof, can be selected. Conditions may include a temperature in the range of 0 ° C to 50 ° C, preferably 25 ° C to 35 ° C; a time of 3 hours to 24 hours, preferably 6 hours to 12 hours; or both. The result of this step is the adsorption of at least a portion of the titanium compound on the conditioned magnesium halide support.
    Finally, two additional metals, hereinafter referred to as "second metal" and "third metal" for convenience, will also be adsorbed onto the magnesium-based support. The "second metal" and the "third metal" are independently selected from zirconium (Zr), hafnium (Hf), vanadium (V), niobium (Nb), tantalum (Ta), chromium (Cr), molybdenum (Mo), and tungsten (W). These metals can be incorporated into any of a variety of forms known to those skilled in the art, but generally the contact between the conditioned magnesium-based halide support including titanium and the selected second and third metals, for example, in the liquid phase, such as an appropriate hydrocarbon solvent, it will be suitable for ensuring the deposition of additional metals to form what can now be called "pro-catalyst", which is a multimetal pro-catalyst.
    The multimetal pro-catalyst has a specific molar ratio that appears to be an important feature to ensure desirable polymer properties that can be attributed to the catalyst prepared with the pro-catalyst. Specifically, the pro-catalyst desirably exhibits a molar ratio of magnesium to a combination of titanium and the second and third metals ranging from 30: 1 to 5: 1; under conditions sufficient to form a multimetal pro-catalyst. Thus, the total molar ratio of magnesium to titanium ranges from 8: 1 to 80: 1.
    After the pro-catalyst is formed, it can be used to form a final catalyst by combining it with a cocatalyst consisting of at least one organometallic compound, such as an alkyl or haloalkyl aluminum, an alkyl aluminum halide, a Grignard reagent, a alkali metal hydride, alkali metal borohydride, alkali metal hydride, alkaline earth metal hydride, or the like. The formation of the final catalyst for the reaction of the pro-catalyst and the organometallic cocatalyst can be carried out in situ, or shortly before entering the polymerization reactor. Thus, the combination of the cocatalyst and the pro-catalyst can occur under a variety of conditions. Such conditions may include, for example, contacting them under an inert atmosphere, such as nitrogen, argon or other inert gas at temperatures in the range of 0 ° C to 250 ° C, preferably 15 ° C to 200 ° C. In preparing the catalytic reaction product, it is necessary to separate soluble hydrocarbon components from insoluble hydrocarbon components. The time for contact between the pro-catalyst and the cocatalyst may desirably vary, for example, from 0 to 240 seconds, preferably from 5 to 120 seconds. Various combinations of these conditions can be employed.
    After the catalyst compositions of the invention have been prepared, they are suitable for use in olefin polymerizations. In specific embodiments, they are polymerizations in paste (in which the polymer is not dissolved in the carrier) or in solution (in which the temperature is high enough to solubilize the polymer in the carrier), or similar, to prepare LLDPE. In general, this can generally be carried out in a reaction medium, such as an isoparaffin or other aliphatic hydrocarbon diluents, with the olefin, or a combination of olefins, being brought into contact with the reaction medium in the presence of the selected catalyst, preferably as a single catalyst. Conditions can be any appropriate, and a molecular weight regulator, often hydrogen, is often present in the reaction vessel to suppress the formation of undesirably high molecular weight polymers.
    The polymers of the present invention can be homopolymers of C2-C20 alpha-olefins, such as ethylene, propylene or 4-methyl-1-pentene, or they can be ethylene or propylene interpolymers with at least one or more alpha-olefins and / or acetylenically unsaturated C2-C20 monomers and / or C4-C18 diolefins. They can also be ethylene interpolymers with at least one of the above C3-C20 alpha-olefins, diolefins and / or acetylenically unsaturated monomers in combination with other unsaturated monomers. Those skilled in the art will understand that selected monomers are desirably those that do not destroy conventional Ziegler-Natta catalysts. For example, in one embodiment, ethylene or a mixture of ethylene is from about 0.1 to about 20 weight percent (weight%), for example, from about 0.1 to about 15 weight percent, or alternatively, from about 0.1 to about 10% by weight; or alternatively, from 0.1 to about 5 weight percent of 1-hexene, 1-octene, or similar superior olefin, based on the total monomer in the final copolymer, can be successfully polymerized using the process of the invention.
    In the polymerization process employing the aforementioned catalytic reaction product, the polymerization is carried out by adding a catalytic amount of the catalyst composition of the invention to a polymerization reactor containing the selected alpha-olefin monomer, or vice versa. The polymerization reactor is maintained at temperatures in the range of 150 ° C to 300 ° C, preferably at solution polymerization temperatures, for example, from 150 ° C to 250 ° C, for a residence time, in certain non-restrictive embodiments , ranging from 5 minutes to 20 minutes. Longer or shorter residence times can alternatively be employed. It is generally desirable to conduct polymerization in the absence of moisture and oxygen and in the presence of a catalytic amount of the catalytic reaction product that is typically in the range of 0.0001 to about 0.01 milligram-transition metal atoms per liter of diluent. It is understood, however, that the most advantageous catalyst concentration will depend on polymerization conditions, such as temperature, pressure, solvent and the presence of catalyst poisons, and that the range mentioned above is given only for the purpose of illustrating a specific embodiment, but not restrictive.
    The pressures can be, for example, relatively low, for example, from 1.0 to 20.7 MPa (150 to 3000 psig), preferably from 1.7 to 6.9 MPa (250 to 1,000 psig), most preferably from 3.1 to 5.5 MPa (450 to 800 psig). (However, polymerization within the scope of the invention can occur at atmospheric pressures at pressures determined by the capabilities of the polymerization equipment.
    Generally in the polymerization process, a carrier which can be an inert organic solvent or diluent or surplus monomer is generally employed. Generally, care must be taken to avoid over-saturation of the solvent with polymer. If such saturation occurs before the catalyst is depleted, the full efficiency of the catalyst may not be realized. In specific embodiments, it may be preferable that the amount of polymer in the carrier does not exceed 30 percent, based on the total weight of the reaction mixture. It may also be very desirable to stir the polymerization components to obtain the desired levels of temperature control and to increase the uniformity of the polymerization throughout the polymerization zone. For example, in the case of relatively faster reactions with relatively active catalysts, means can be provided to reflux monomer and diluent, if diluent is included, thus removing some of the reaction heat. In any case, suitable means must be provided to dissipate the exothermic heat of polymerization. Thus, the polymerization can be carried out in batches, or in a continuous way, such as, for example, passing the reaction mixture through an elongated reaction tube externally contacted with appropriate cooling medium to maintain the desired reaction temperature, or passing the reaction mixture through a balance reactor or a series of them.
    To increase the catalytic efficiency in the polymerization of ethylene, it may also be desirable to maintain a certain concentration of ethylene in the diluents to ensure stability of the reactor and, preferably, to optimize the catalytic efficiency. In some embodiments, this may include a solvent to ethylene ratio ranging from 1: 2 to 1: 8, preferably from 1: 3 to 1: 5. To achieve this when excess ethylene is fed into the system, some ethylene can be discharged.
    Hydrogen is often used in the practice of the present invention, in order to reduce the molecular weight of the resulting polymer. For the purposes of the present invention, it is beneficial to employ hydrogen in the polymerization mixture in concentrations preferably ranging from 0.001 to 1 mol per mole of monomer. Larger amounts of hydrogen within this range can be useful to produce polymer with generally lower molecular weight. It is generally known to those skilled in the art that hydrogen can be added to the polymerization vessel, either as a monomer stream, or separately from it, before, during or after the addition of the monomer to the polymerization vessel. However, in preferred embodiments, it is highly desirable to ensure that hydrogen is added before or during the addition of the catalyst, in the range of 200,000 to 3 million grams of polymer per gram of Ti, such as, for example, 600,000 to 2 million grams of polymer per gram of Ti.
    The resulting polymer can be effectively recovered from the polymerization mixture by eliminating the unreacted monomer and diluent, when used. No further removal of impurities is necessary. The resulting polymer can contain small amounts of catalytic residue as shown in the examples below and also has a relatively narrow molecular weight distribution. The resulting polymer can also be sieved by melting. After the melting process in the extruder, the molten composition is passed through one or more active sieves, placed in series of more than one, with each active sieve having a micronic retention size of about 2pm to about 400 pm (2 to 4 x 10'5 m), and preferably from about 2 pm to about 300 pm (2 to 3 xm) and most preferably from about 2 pm to about 70 pm (2 to 7 xm), at a flow mass of about 1.0 to about 20 kg / s / m2 (5 to about 100 lb / h / square inch). Such a melting sieve is described in U.S. Patent No. 6,485,662, incorporated herein by reference to the extent that it describes melting sifting.
    The resulting polymer can, in certain particularly preferred embodiments, be prepared in a manner that has properties that include a polydispersity less than 3.50 and an MWCCR less than 1.10, preferably 0.75 to 1.10. The resulting polymer can optionally have a high density fraction of less than 25 weight percent.
    The polyethylene composition according to the present invention has a density in the range of 0.900 to 0.960 g / cm 3 . All values and individual sub-ranges from 0.900 to 0.960 g / cm 3 are included and described here; for example, the density can be from a minimum limit of 0.900, 0.911, 0.919, 0.923 0.928, or 0.936 g / cm 3 to a maximum limit of 0.941, 0.947 0.954, 0.959, or 0.960 g / cm 3 . For example, the polyethylene composition can have a density in the range of 0.905 to 0.945 g / cm 3 ; or alternatively, the polyethylene composition can have a density in the range of 0.910 to 0.935 g / cm 3 ; or alternatively, the polyethylene composition can have a density in the range of 0.915 to 0.925 g / cm 3 .
    The polyethylene composition according to the invention has a molecular weight distribution (Mw / Mn) (measured according to the conventional GPC method) in the range of 2.6 to 4.2. All values and individual sub-ranges from 2.6 to 4.2 are included and described here; for example, the molecular weight distribution (Mw / Mn) can be from a minimum limit of 2.6, 2.8, 3.0, 3.2, or 3.3, to a maximum limit of 2.8, 3.0, 3.2, 3.3, 3.8 or 4.2. In a non-restrictive example, the polyethylene composition can have a molecular weight distribution (Mw / Mn) in the range of 2.6 to 3.6; or alternatively, the polyethylene composition can have a molecular weight distribution (M „/ Mn) in the range of 2.6 to 3.2.
    The polyethylene composition according to the present invention has a melt index (I2) in the range of 0.1 to 50 g / 10 minutes. All values and individual sub-ranges from 0.1 to 50g / 10 minutes are included and described here; for example, the melt index (I2) can be from a lower limit of 0.1, 0.5, 0.8, 1, 2, 3, 5, 6, 7, or 8 g / 10 minutes, at a maximum limit of 0.5, 0.8, 1, 2, 3, 5, 6, 7, 8 or 10 g / 10 minutes. In a non-restrictive example, the polyethylene composition can have a melt index (I2) in the range of 0.2 to 20 g / 10 minutes; or alternatively, the polyethylene composition can have a melt index (I2) in the range of 0.5 to 5 g / 10 minutes.
    The polyethylene composition according to the present invention has a melt flow ratio (I10 / I2) in the range of 6 to 12. All individual values and sub-ranges of 6 to 12 are included and described herein; for example, the melt flow ratio (I10 / I2) can be from a minimum limit of 6, 7, 8, 9, 10 or 11 to a maximum limit of 7, 8, 9, 10, 11 or 12. For For example, the polyethylene composition can have a melt flow ratio (I10 / I2) in the range of 6 to 10; or alternatively, the polyethylene composition may have a melt flow ratio (I10 / I2) in the range of 6.5 to 8.
    The polyethylene composition according to the present invention has a molecular weight (Mw) in the range of 50,000 to 300,000 daltons.
    The polyethylene composition can have a molecular weight at a density ratio (MWCCR) in the range of 0.75 to 1.10. All values and individual sub-ranges from 0.75 to 1.10 are included and described here; for example, the polyethylene composition can have a MWCCR in the range of 0.75, 0, 80, 0.85, 0, 90, 1.0 or 1.05 to 0, 80, 0.85, 0, 90, 1.0, or 1.1. The polyethylene composition can have a vinyl unsaturation in the range of 0.10 to 0.50 vinyls per thousand carbon atoms present in the main chain of the polyethylene composition. All individual values and sub-ranges from 0.15 to 0.35 are included and described here; for example, the polyethylene composition may have a vinyl unsaturation of less than 0.20 vinyl per thousand carbon atoms present in the main chain of the polyethylene composition; or alternatively, the polyethylene composition may have a vinyl unsaturation of less than 0.30 vinyls per thousand carbon atoms present in the main chain of the polyethylene composition.
    The polyethylene composition can comprise less than 20 weight percent units derived from one or more alpha-olefin comonomers. All individual values and sub-ranges of less than 20 weight percent are included and described here; for example, the polyethylene composition can comprise less than 15 weight percent units derived from one or more alpha-olefin comonomers; or alternatively, the polyethylene composition may comprise less than 12 weight percent units derived from one or more alpha-olefin comonomers; or alternatively, the polyethylene composition may comprise less than 9 weight percent units derived from one or more alpha-olefin comonomers; or alternatively, the polyethylene composition may comprise less than 7 weight percent units derived from one or more alpha-olefin comonomers; or alternatively, the polyethylene composition may comprise less than 5 weight percent units derived from one or more alpha-olefin comonomers; or alternatively, the polyethylene composition may comprise less than 3 weight percent units derived from one or more alpha-olefin comonomers; or alternatively, the polyethylene composition may comprise less than 1 weight percent of units derived from one or more alpha-olefin comonomers; or alternatively, the polyethylene composition may comprise less than 0.5 weight percent units derived from one or more alpha-olefin comonomers.
    Alpha-olefin comonomers typically have no more than 20 carbon atoms. For example, alpha-olefin comonomers may preferably have 3 to 10 carbon atoms, and more preferably 3 to 8 carbon atoms. Representative alpha-olefin comonomers include, but are not limited to, propylene, 1-butene, 1-pentene, 1-hexene, 1-octene, 1-nonene, 1-decene, and 4-methyl-1-pentene. The one or more alpha-olefin comonomers can, for example, be selected from the group consisting of propylene, 1-butene, 1-hexene, and 1-octene; or alternatively, the group consisting of 1-hexene and 1-octene.
    The polyethylene composition can comprise at least 80 weight percent ethylene derived units. All individual values and sub-ranges of at least 80 weight percent are included and described here; for example, the polyethylene composition can comprise at least 88 weight percent of ethylene-derived units; or alternatively, the polyethylene composition can comprise at least 89 percent units derived from ethylene; or alternatively, the polyethylene composition can comprise at least 91 weight percent ethylene derived units; or alternatively, the polyethylene composition can comprise at least 93 weight percent ethylene-derived units; or alternatively, the polyethylene composition may comprise at least 95 weight percent ethylene-derived units; or alternatively, the polyethylene composition can comprise at least 97 weight percent of ethylene-derived units; or alternatively, the polyethylene composition can comprise at least 99 weight percent ethylene-derived units; or alternatively, the polyethylene composition can comprise at least 99.5 weight percent ethylene derived units.
    The polyethylene composition of the present invention is substantially free of any long chain branches, and preferably, the polyethylene composition of the present invention is free of any long chain branches. Substantially free of any long chain branch, as used herein, refers to a polyethylene composition preferably substituted with less than about 0.01 long chain branch per 1000 total carbons, and more preferably, less than about 0.001 branch long chain with 1000 total carbons. Alternatively, the polyethylene composition of the present invention is free of any long chain branches.
    The polyethylene composition can also comprise a value equal to or greater than 1 part by combined weight of at least three remaining metal residues of the multimetal polymerization catalyst per one million parts of polyethylene composition, where such metals are selected from the group consisting of titanium , zirconium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum, tungsten, and their combinations, with each metallic residue present in at least 0.4 ppm, for example, in the range of 0.4 to 5 ppm. All values and individual sub-ranges equal to or greater than 1 ppm are included and described here; for example, the polyethylene composition may also comprise a value equal to or greater than 2 parts by combined weight of at least three remaining metal residues of the multimetal polymerization catalyst per one million parts of polyethylene composition. The at least three metal residues remaining from the multimetal polymerization catalyst in the polyethylene composition of the invention can be measured by X-ray fluorescence (XFR) calibrated to reference standards. The polymeric resin granules were molded by compression at elevated temperature into plates about 0.95 cm (inch) thick for measuring X-rays in a preferred method. At very low concentrations of metal, such as below 0.1 ppm, ICP-AES would be an appropriate method for determining metal residues present in the polyethylene composition of the invention.
    In one embodiment, the polyethylene composition according to the invention, may have 2 or more peaks in an elution temperature-eluted quantity curve determined using the elution fraction method and continuous temperature rise equal to or greater than 30 ° C , where the purging peak, which is below 30 ° C, is excluded.
    The polyethylene composition of the invention can also comprise additional components such as other polymers and / or additives. These additives include, but are not restricted to antistatic agents, color enhancers, dyes, lubricants, fillers, pigments, primary antioxidants, secondary antioxidants, processing aids, UV stabilizers, and combinations thereof. The polyethylene composition of the invention can contain any amount of additives. The polyethylene composition of the invention can comprise from about 0 to about 10 percent by weight combined of such additives, based on the weight of the polyethylene composition of the invention, including such additives. All individual values and sub-ranges from about 0 to about 10 weight percent are included and described herein; for example, the polyethylene composition of the invention can comprise from 0 to 7 percent by weight combined of additives, based on the weight of the polyethylene composition of the invention, including such additives; alternatively, the polyethylene composition of the invention can comprise from 0 to 5 percent by weight of combined additives, based on the weight of the polyethylene composition of the invention, including such additives; or alternatively, the polyethylene composition of the invention can comprise from 0 to 3 percent by weight combined of additives, based on the weight of the polyethylene composition of the invention, including such additives; or alternatively, the polyethylene composition of the invention can comprise from 0 to 2 percent by weight combined of additives, based on the weight of the polyethylene composition of the invention, including such additives; or alternatively, the polyethylene composition of the invention can comprise from 0 to 1 percent by weight combined of additives, based on the weight of the polyethylene composition of the invention, including such additives; or alternatively, the polyethylene composition of the invention can comprise from 0 to 0.5 percent by weight combined of additives, based on the weight of the polyethylene composition of the invention, including such additives. Antioxidants, such as Irgafos ™ 168 and Irganox ™ 1010, can be used to protect the polyethylene composition of the invention from thermal and / or oxidative degradation. Irganox ™ 1010 is tetracis (methylene (3,5-di-ter-butyl-4-hydroxyhydrocinamate) from Ciba Geigy Inc. Irgafos ™ 168 is tris (2,4-di-butylphenyl) phosphite from Ciba Geigy Inc.
    Any conventional ethylene (co) polymerization reaction can be employed to produce the polyethylene composition of the invention. These conventional ethylene (co) polymerization reactions include, but are not restricted to, the pasty phase polymerization process, the solution phase polymerization process, and combinations thereof, using one or more conventional reactors, for example, loop reactors, agitated tank reactors, batch batch reactors, series, and / or any combinations thereof. In one embodiment, the polymerization reactor can comprise two or more reactors in series, parallel or combinations thereof. In one embodiment, the polymerization reactor is a single reactor.
    The polymers produced by the present invention can include a wide variety of products including, in specific embodiments, LLDPE, but also high density polyethylenes (HDPE), plastomers, medium density polyethylene, proppropylene and polypropylene copolymers. For these and other applications, articles can be prepared showing improved overall quality due to the narrower polydispersity and narrower molecular weight distribution of the polymer in relation to density. Useful forming operations for polymers may include, but are not limited to, film, sheet, tube and fiber extrusion and coextrusion, as well as blow molding, injection molding and rotary molding. Films include blown or coextruded or laminated films useful as retractable film, cling film, stretch film, sealant film, oriented film, snack / snack packaging, reinforced bags, grocery bags, baked and frozen food packaging, packaging for medical use, industrial ceilings, film applications in agriculture, and membranes, for example, applications in contact with food and without contact with food. Fibers include cast spinning operations, solution spinning and cast blown fiber operations for use in woven and non-woven forms for the manufacture of filters, diaper fabrics, medical apparel and geotextiles. Extruded items include tubing / probe for medical use, coatings for wires and cables, geomembranes and coatings for wells. Molded items include monolayer and multilayer constructions in the form of bottles, tanks, large hollow articles, rigid containers for food and toys. Examples
    Two samples of the catalysts of the invention are prepared using the protocols presented below (Examples 1 and 2) and three samples of catalysts not of the invention are prepared using their protocols (Comparative Examples A-C). All five catalysts are then used for the preparation of LLDPE polymer in solution polymerization, and then the LLDPE polymer is used in the preparation of blown film. The test is conducted both on the LLDPE polymer and on the blown film, as previously described. Example 1
    To 800 ml of MgCl2 (0.20 M in ISOPAR ™ E) was added (C2Hs) A1C12 (40 ml of a 1.0 M solution in hexane). (ISOPAR ™ is a registered trademark of ExxonMobil Chemical. ISOPAR ™ E is a colorless isoparaffinic fluid). The resulting mixture is allowed to stir overnight at room temperature. TiCl4 solutions (16 ml of 0.25 M solution in ISOPAR ™) and VOC13 (32 ml of a 0.25 M solution in ISOPAR ™) are mixed and then added to the magnesium / aluminum suspension, followed by a Zr solution (TMHD) 4 (bis (2,2,6,6-tetramethyl-3, 5-heptanedionate) zirconium, 8 ml of a 0.25M solution in ISOPAR ™ E). The resulting mixture is allowed to stir overnight to complete aging of the pro-catalyst. Example 2
    To 800 ml of MgCla (0.20 M in ISOPAR ™) A1C12 (C2Hs) is added (24 ml of a 1.0 M solution in hexane). The resulting mixture is allowed to stir overnight at room temperature. The TiCl4 solutions (16 ml of a 0.25 M solution in ISOPAR ™ E) and VOCI3 (32 ml of a 0.25 M solution in ISOPAR ™ E) are mixed and then added to the magnesium / aluminum suspension, followed by a solution of Hf (TMHD) 4 bis (2,2,6,6-tetramethyl-3,5-heptanedionate) hafnium, 8 ml of a 0.25 M solution in ISOPAR ™ E). The resulting mixture is allowed to stir overnight to complete aging of the pro-catalyst. Comparative Example A
    To 800 ml of MgC12 (0.20 M in ISOPAR ™ E) is added (C2H5) A1C12 (48 ml of a 1.0 M solution in hexane). The resulting mixture is allowed to stir overnight at room temperature. A solution of Ti (OiPr) 4 (titanium isopropoxide, 48 ml of a 0.25 M solution in ISOPAR ™ E) is then added to the magnesium / aluminum suspension. The resulting mixture is allowed to stir overnight to complete aging of the pro-catalyst. Comparative Example B
    To 800 ml of MgC12 (0.20 M in ISOPAR ™ E) is added (C2Hs) A1C12 (32 ml of a 1.0 M solution in hexane). The resulting mixture is allowed to stir overnight at room temperature. A solution of TiCI4 (16 ml of a 0.25 M solution in ISOPAR ™ E) is then added to the magnesium / aluminum suspension. The resulting mixture is allowed to stir overnight to complete aging of the pro-catalyst. Comparative Example C
    To 800 milliliters (ml) of MgC12 (0.20 M in ISOPAR ™ E) was added (C2Hs) A1C12 (32 ml of a 1.0 M solution in hexane). The resulting mixture was allowed to stir overnight at room temperature. Solutions of titanium chloride (16 ml of a 0.25 M solution in ISOPAR ™ E) and VOCI3 (32 ml of a 0.25 M solution in ISOPAR ™ E) are mixed and then added to the magnesium / aluminum suspension. The resulting mixture is allowed to stir overnight to complete aging of the pro-catalyst.
    Each of the catalysts previously prepared is then used in the preparation of LLDPE polymer using the typical solution polymerization method. In this method, three feeds - ethylene, hydrogen and octene - are conducted at a rate as shown in Table 1 previously mentioned in a polymerization zone maintained at a temperature of 185 ° C. The three flow rates are adjusted to produce a copolymer with a target I2 of 1.0 and a density of 0.920 g / cm 3 .
    As shown in Table 1, Examples 1 and 2 show improved catalytic efficiency (EFF) when compared to that of Comparative Examples A and B. Examples 1 and 2 also show significantly narrower polydispersity (PDI less than 3.5, Table 1 ) compared to the Comparative Examples, and also lower molecular weight at a density ratio (Mw of high density fraction to M „of low density fraction, Table 2).
    The weight and number average molecular weights (Mn and Mw, respectively) and polydispersity (Mw / Mn) of the polymers are determined by Gel Permeation Chromatography (GPC). The column and carousel compartments are operated at 140 ° C. The columns are 4 columns of 10 microns PL Gel Mixed B. The solvent is 1,2,4-trichlorobenzene. The samples are prepared at a concentration of 0.1 g of polymer in 50 ml of solvent. The chromatographic solvent and the sample preparation solvent contain 200 ppm of butylated hydroxytoluene (BHT). The two sources of solvent are sparged with nitrogen. The samples are stirred for 2 hours at 160 ° C. The injection volume is 100 pl and the flow rate is 1.0 mL / min. Gel permeation chromatography (GPC)
    The weight and number average molecular weights (Mn and Mw, respectively) and the polydispersity (Mw / Mn) of the polymers are determined using Gel Permeation Chromatography (GPC). The chromatographic system consists of a Model PL-210 and Model PL-220 high temperature chromatograph from Polymer Laboratories. Data collection is performed using Viscotek software (Housten, TX) TriSEC version 3 and a Viscotek DM400 4-Channel Data Manager. The system is equipped with an online solvent degassing device from Polymer Laboratories.
    The column and carousel compartments are operated at 140 ° C. The columns used are 4 columns of 10 microns 4PL Gel Mixed-B. The solvent used is 1,2,4-trichlorobenzene. The samples are prepared at a concentration of 0.1 g of polymer in 50 ml of solvent. The chromatographic solvent and the sample preparation solvent contain 200 ppm of butylated hydroxytoluene (BHT). The two sources of solvent are sparged with nitrogen. The samples are stirred for 2 hours at 160 ° C. The injection volume used is 100 pL and the flow rate is 1.0 mL / min. Calibration of the GPC column set is conducted with polystyrene standards with narrow MWD with molecular weights ranging from 580 to 8,400,000 g / mol, purchased from Polymer Laboratoris (Shropshire, UK). Data reduction is carried out with Viscotek TriSEC software. The peak molecular weights of the polystyrene standard are converted to molecular weights of polyethylene using the method described in Williams, T., and Ward, IM, "The Construction of Polyethylene Calibration Curve for Gel Permeation Chromatography Using Polyestyrene Fractions", J. Polym . Sci. Polym. Lett. 6, 621 (1968): M polyethylene = A (Polystyrene) B where M is the molecular weight, A has a value of 0.4316 and B is equal to 1.0. Calculations of equivalent molecular weight of polyethylene are performed using Viscotek TriSEC Version 3.0 software. CEF Method
    The comonomer distribution analysis is conducted with Elution and Crystallization Fractionation (CEF). The method includes first combining ortho-dichlorobenzene (ODCB) with 600 ppm of butylated hydroxytoluene (BHT) antioxidant used as a solvent. The samples are prepared using an automatic sampler at 160 ° C for 2 hours under agitation at 4 mg / mL). The injection volume is 300 microliters. The temperature profile used for CEF is as follows: crystallization at 3 ° C / min from 110 ° C to 30 ° C; thermal equilibrium at 30 ° C for 5 minutes; and elution at 3 ° C / min from 30 ° C to 140 ° C. The flow rate during crystallization is 0.052 ml / min and during elution 0.50 ml / min. The data is collected at a data point / second.
    I2 índice de fluxo de fundido de acordo com ASTM D1238; dg/min (190ºC, 2,16 kg) I10 índice de fluxo de fundido testado de acordo com ASTM D1238; dg/min (190ºC, 10 kg) Relação de fluxo de fundido I10/I2 calculada a partir dos índices de fluxo de fundido I10 e I2 Densidade testada de acordo com ASTM D792 Método B; g/cm3 PDI = peso molecular médio ponderal/peso molecular médio numérico The CEF column is loaded with 125 pm ± 6% acid-washed glass beads with 0.32 cm (") stainless steel tubing. The injection volume is 2.06 ml. Column temperature calibrations are conducted using a mixture of linear polyethylene Standard Reference Material NIST 1475a (1.0 mg / mL) and Eicosane (2 mg / mL) in ODCB The temperature is calibrated by adjusting the elution heating rate so that the NIST linear polyethylene 1475a has a peak temperature at 101.0 ° C and Eicosane has a peak temperature at 30.0 ° C. The CEF column resolution is calculated with a mixture of NIST 1475a linear polyethylene (1.0 mg / ml) and hexacontane (> 97.0% purity, 1 mg / ml). A reference line separation of hexacontane and polyethylene NIST 1475a is obtained. The area of hexacontane (from 35.0 ° C to 67.0 ° C) up to NIST 1475a area from 67.0 ° C to 110.0 ° C is determined to be 50:50, with the amount of soluble fraction below 35 ° C being less than 1.8% by weight. in 6.0.

    I2 melt flow index according to ASTM D1238; dg / min (190ºC, 2.16 kg) I10 melt flow index tested according to ASTM D1238; dg / min (190ºC, 10 kg) Melt flow ratio I10 / I2 calculated from melt flow indexes I10 and I2 Density tested according to ASTM D792 Method B; g / cm 3 PDI = weight average molecular weight / number average molecular weight
    % HD calculation
    The high density fraction% HD is determined from the CEF graph, calculated as the weight fraction (W) of the polymer eluting between temperature (T) from 93 ° C to 110 ° C:
    MWCCR calculation
    The molecular weight of the comonomer content ratio (MWCCR) is defined as the average Mw of a low density fraction (eluting from 60 ° C to 70 ° C in the CEF graph for copolymers with densities greater than 0.910 g / cm 3 and eluting from 30 ° C to 60 ° C in the CEF graph for copolymers with densities less than 0.910 g / cm 3 ) divided by the global Mw of the copolymer, as determined using GPC.
    For copolymers with a density greater than 0.910 g / cm 3 :
    For copolymers with a density less than 0.910 g / cm 3 :
    Samples of LLDPE polymer beads prepared for Examples 1 and 2 and Comparative Examples A-C are subjected to analysis by neutron activation. Approximately 3.5g of the polymer is transferred to pre-cleaned 2-drachma polyethylene bottles. Standard aliquots of Al, Mg, Ti, V, Hf and Zi standards are prepared from their standard solutions (National Institute of Standards and Technology (NIST), SPEX CertiPrep Group traceable standard solutions) and also placed in polyethylene bottles of 2 drachmas. Each vial is diluted with milli-Q Pure water to 6 ml and the vials are thermally sealed. The samples and standards are then analyzed after standard NAA procedure, Global-SOP-OllOl.01 for the data elements, using the Mark I TRIGA ™ nuclear reactor. (TRIGA ™ is a trademark of General Atomics).
    For analysis of Al, Mg, Ti, Hf, Zr and V, the samples are transferred to non-irradiated flasks before gamma spectroscopy. The reactions and experimental conditions used for each element are described in Table 2. Elemental concentrations are calculated using CANBERRA ™ software (Canberra ™ is a brand of Canberra, a company of the Areva Group) and standard comparative technique, and the results are shown in Table 3.
    The interference correction is conducted for the interference of aluminum with magnesium, using the CANBERRA ™ software. Table 2
    The polymers produced in Examples 1 and 2 and Comparative Examples A-C are also processed via the blown film extrusion process on a Collin triple layer film line. The blown film line consists of three groove feed extruders with single thread threads (25:30:25 mm). The length / diameter ratio for all threads is 25: 1. The blown film line has a 60 mm die with a double edge air ring cooling system. The matrix has an opening of 2 mm. The films are blown with a blowing ratio of up to 2.5 and an ice line height of 17.78 cm (7 inches). The film thickness is 50 µm (2 mils) and the useful width of the films is about 23.5 cm. Table 3.
    The products of this protocol are correspondingly labeled as Examples 3 and 4 and Comparative Examples D-F. The films are then tested and the results recorded in Table 3. Table 3
    Resist. Dart impact A, according to ASTM D1709, using a 3.81 cm (1.5 ") diameter dart head, with a maximum drop of 66.04 cm (26").
    Tear resistance MD and CD: Elmendorf test, according to ASTM D1922, based on an electronic tear resistance tester from Thwing-Albert.
    Opacity: according to ASTM D1003; measurements made on a Haze Gard instrument from BYD-Gardner Company.
    Brightness at 20 and Brightness at 40 °: according to ASTM D2457.
    Table 3 shows significantly better optical properties, particularly Brightness at 20 and Brightness at 40, obtained with the trimetallic catalyst of Examples 3 and 4 of the invention, in comparison with Comparative mono and bimetallic D-F catalysts. This improvement can be attributed to the reduced polydispersity and molecular weight in a density ratio found in the polymers prepared with the catalysts. Example 4 also shows improved Dart A impact resistance, making the combination of Dart A impact and optical improvements, while maintaining Elmendorf dart resistance as an attractive option for some applications.
    权利要求:
    Claims (11)
    [0001]
    Process for preparing a multimetal pro-catalyst, characterized by the fact that it comprises:
    (a) reacting a hydrocarbon-soluble organomagnesium compound or its complex and an active non-metallic or metallic halide to form a halogenated magnesium support;
    (b) contacting the magnesium halide support with a conditioning compound containing an element selected from the group consisting of boron, aluminum, gallium, indium and tellurium, in sufficient conditions to form a conditioned magnesium halide support;
    (c) contacting the conditioned magnesium halide support and a compound containing, as the first metal, titanium, to form a supported titanium compound;
    (d) contacting the supported titanium compound and a second metal and a third metal independently selected from the group consisting of zirconium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum and tungsten, provided that the second metal and the third metal are not equals; and as long as the molar ratio of magnesium to a combination of titanium and the second and third metals varies from 30: 1 to 5: 1, under conditions sufficient to form a multimetal pro-catalyst.
    [0002]
    Multimetal pro-catalyst, characterized by the fact that it is obtained according to the process, as defined in claim 1.
    [0003]
    Pro-catalyst, according to claim 2, characterized in that the molar ratio of magnesium to titanium varies from 8: 1 to 80: 1.
    [0004]
    Multimetal polymerization catalyst, characterized by the fact that it comprises the reaction product of the multimetal pro-catalyst, as defined in claim 2, and an organometallic cocatalyst.
    [0005]
    Polyethylene polymer, characterized by the fact that it is prepared through a process in which ethylene and, optionally, one or more olefinic comonomers, are polymerized in the presence of the multimetal polymerization catalyst, as defined in claim 4.
    [0006]
    Polymer, according to claim 5, characterized by the fact that it has a polydispersity (PDI) of less than 3.5, and a MWCCR in the range of 0.75 to 1.10.
    [0007]
    Polymer according to either of claims 5 or 6, characterized in that it comprises a value equal to or greater than 1 part by combined weight of at least three remaining metallic residues of the multimetal polymerization catalyst per one million parts of polyethylene polymer , and such metals are selected from the group consisting of titanium, zirconium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum, tungsten and their combinations, and each said residual metal is present at least 0.4 ppm. or
    [0008]
    Polymer according to any one of claims 5 or 6, characterized in that said polyethylene has the following properties:
    (a) a density in the range of 0.900 to 0.960 g / cm 3 ; or
    (b) a melting index (I2) in the range of 0.1 to 50 g / 10 minutes; or
    (c) a melt flow ratio (I10 / I2) in the range of 6 to 10.
    [0009]
    Polymer according to either of claims 5 or 6, characterized in that said polyethylene has the following properties: (a) a density in the range of 0.900 to 0.960 g / cm 3 ; or (b) a melting index (I2) in the range of 0.1 to 50 g / 10 minutes; (c) a melt flow ratio (I10 / I2) in the range of 6 to
    [0010]
    Composition, characterized in that it comprises polyethylene polymer, as defined in any one of claims 5 or 6, and one or more polymers or one or more additives.
    [0011]
    Article, characterized by the fact that it comprises the polyethylene polymer, as defined in any of claims 5 or 6.
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    法律状态:
    2018-04-03| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|
    2019-10-22| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]|
    2020-04-14| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|
    2020-06-23| B16A| Patent or certificate of addition of invention granted|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 23/05/2012, OBSERVADAS AS CONDICOES LEGAIS. |
    优先权:
    申请号 | 申请日 | 专利标题
    US201161491924P| true| 2011-06-01|2011-06-01|
    US61/491,924|2011-06-01|
    PCT/US2012/039140|WO2012166469A1|2011-06-01|2012-05-23|Multi -metallic ziegler - natta procatalysts and catalysts prepared therefrom for olefin polymerizations|
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