Polymerization of a purge stream containing 1-octene

Abstract

The present disclosure provides a process. In one embodiment, the process includes providing a purge stream containing octene monomer. The process includes contacting the purge stream with a bis-biphenylphenoxy catalyst under polymerization conditions and producing a bis-biphenylphenoxy copolymer having an absolute weight average molecular weight (Mw) of greater than 1,300,000 g / mol. (Abs) ) and Mw of 1.3 to 3.0 (Abs) / Mn (Abs) and forming an octene polymer having:

Description

[Background technology]

[0001] In the production of ethylene / octene copolymers, ethylene, octene comonomer, and a polymerization catalyst are introduced into a polymerization reactor under suitable reaction conditions (in the presence of a solvent and a chain transfer agent) to obtain a polymerization product stream of ethylene / octene copolymer. The product stream is removed from the reactor. The product stream contains the ethylene / octene copolymer and hydrocarbon species, including unreacted monomer (ethylene), unreacted comonomer (octene), and other related hydrocarbons (hydrogen, ethane, methane, propane, pentane, hexane, and butane). The ethylene / octene copolymer is separated from the solvent, unreacted monomer, and unreacted comonomer by devolatilization. The granular ethylene / octene copolymer is then recovered after pelletization and cooling. After the ethylene / octene copolymer is separated from the product stream, the hydrocarbon species are either recycled to the polymerization reactor or purged from the system.

[0002] Regeneration of purged hydrocarbon species is one of the biggest challenges for large-scale polyolefin production. For example, the conversion of octene comonomer in the polymerization of ethylene / octene copolymers is typically very low, e.g., 10-20%. This means that 80-90% of the octene can pass through the reactor without being converted to polymer.

[0003] Ideally, this octene comonomer would be recycled to the polymerization reactor. While recycling volatile monomers such as ethylene is highly efficient, recycling octene is difficult, especially when other saturated hydrocarbons are present in the product stream. The boiling point of octene is very close to that of other saturated and unsaturated species present in the product stream, making separation of octene difficult. Fresh octene streams also contain other isomers of octene (1-5 wt% octene isomers based on the total weight of octene). Octene isomers typically do not react with ethylene in the polymerization process. As a result, octene isomers aggregate or otherwise "build up" in the continuous recycle of the recycle stream, reducing the efficiency of its recycle as a feed stream. In this way, octene isomers can accumulate to up to 70% of the total recycle stream.

[0004] Therefore, it has been recognized in the art that there is currently a need for a method to utilize the hydrocarbon species of the purge stream without simply discarding them. There is a further need to utilize the octene monomer present in the purge stream. Summary of the Invention

[0005] The present disclosure provides a process. In one embodiment, the process includes providing a purge stream containing octene monomer. The process includes contacting the purge stream with a bis-biphenylphenoxy catalyst under polymerization conditions and producing a bis-biphenylphenoxy copolymer having an absolute weight average molecular weight (Mw) of greater than 1,300,000 g / mol. (Abs) ) and Mw of 1.3 to 3.0 (Abs) / Mn (Abs) and forming an octene polymer having:

[0006] The present disclosure provides a composition. In one embodiment, the composition comprises an octene homopolymer and a solvent. The octene homopolymer has an absolute weight average molecular weight (Mw) greater than 1,300,000 g / mol. (Abs) ) and Mw of 1.3 to 3.0 (Abs) / Mn (Abs) It has. [Brief explanation of the drawings]

[0007] [Figure 1] FIG. 1 is a schematic diagram of a polymerization system according to one embodiment of the present disclosure.

[0008] definition Any reference to the Periodic Table of the Elements is to that published by CRC Press, Inc., 1990-1991. References to element groups in this table are by the new notation for numbering groups.

[0009] For purposes of United States patent practice, the contents of any referenced patent, patent application, or publication are incorporated by reference in their entirety (or the equivalent United States version thereof is so incorporated by reference), particularly with respect to the disclosure of definitions (to the extent not inconsistent with any definitions specifically provided in this disclosure) and general knowledge in the art.

[0010] Numerical ranges disclosed herein include all values ​​from the lower limit to the upper limit, inclusive. Ranges containing explicit values ​​(e.g., 1 or 2, or 3-5, or 6, or 7) also include all subranges between any two explicit values ​​(e.g., the 1-7 range above includes 1-2, 2-6, 5-7, 3-7, 5-6, etc.).

[0011] Unless otherwise stated, implied from the context, or customary in the art, all parts and percentages are by weight and all test methods are current as of the filing date of this disclosure.

[0012] As used herein, the term "blend" or "polymer blend" refers to a blend of two or more polymers. Such blends may or may not be miscible (not phase separated at the molecular level). Such blends may or may not be phase separated. Such blends may or may not contain one or more domain configurations as determined from transmission electron spectroscopy, light scattering, X-ray scattering, and other methods known in the art.

[0013] The term "composition" refers to a mixture of materials that comprise the composition, as well as reaction products and decomposition products formed from the materials of the composition.

[0014] The terms "comprising," "including," "having," and their derivatives are not intended to exclude the presence of any additional component, step, or procedure, whether specifically disclosed or not. For the avoidance of doubt, all compositions claimed through the use of the term "comprising" may include any additional additive, adjuvant, or compound, whether polymeric or not, unless stated to the contrary. In contrast, the term "consisting essentially of" excludes any other component, step, or procedure from the scope of any succeeding description, except those that are not essential to operability. The term "consisting of" excludes any component, step, or procedure not expressly delineated or listed. The term "or," unless otherwise stated, refers to the listed members individually as well as in any combination. The use of the singular includes the use of the plural, and vice versa.

[0015] An "ethylene-based polymer" is a polymer that contains greater than 50 weight percent (wt%) polymerized ethylene monomer (based on the total amount of polymerizable monomers) and may optionally contain at least one comonomer. Ethylene-based polymers include ethylene homopolymers and ethylene copolymers (meaning units derived from ethylene and one or more comonomers). The terms "ethylene-based polymer" and "polyethylene" may be used interchangeably.

[0016] As used herein, the term "1-octene" has the molecular formula CH 16 1-octene is an unsaturated hydrocarbon α-olefin having the unsaturation in the alpha position. 1-octene has the molecular structure (A) shown below. [ka]

[0017] As used herein, the term "octene isomers" refers to isomers of the molecular formula CH 16 where the unsaturation (double bond) is not in the alpha position. In other words, the term "octene isomer" refers to any octene excluding 1-octene. Non-limiting examples of octene isomers include cis-2-octene, trans-2-octene, cis-3-octene, trans-3-octene, and combinations thereof, as well as cis-4-octene, trans-4-octene, branched octene isomers, and combinations thereof.

[0018] An "octene-based polymer" is a polymer that contains greater than 50 weight percent (wt%) polymerized octene monomer (based on the total amount of polymerizable monomers), and optionally at least one comonomer different from octene (C 2~7 α-olefin and / or C 9~12The octene-based polymer may contain octene homopolymers and octene copolymers (meaning units derived from octene and one or more comonomers). The terms "octene-based polymer" and "polyoctene" may be used interchangeably.

[0019] A "polymer" is a compound prepared by polymerizing monomers, whether of the same or different types, that provide multiple and / or repeating "units" or "mer units" that, in polymerized form, constitute the polymer. Thus, the general term polymer encompasses the term homopolymer, which is commonly used to refer to a polymer prepared from only one type of monomer, and the term copolymer, which is commonly used to refer to a polymer prepared from at least two types of monomer. It also encompasses all forms of copolymers, e.g., random, block, etc. The terms "ethylene / α-olefin polymer" and "octene / α-olefin polymer" refer to the aforementioned copolymers prepared from polymerizing ethylene or octene with one or more additional polymerizable α-olefin monomers, respectively. While polymers are often referred to as "made with" one or more specific monomers, "based on" a particular monomer or monomer type, "containing" a particular monomer content, etc., it should be noted that in this context, the term "monomer" is understood to refer to the polymerized residue of a particular monomer, not to the unpolymerized species. Generally, polymers herein are referred to in terms of "units" that are the polymerized form of the corresponding monomers. Test Method Gel Permeation Chromatography (GPC)

[0020] The chromatography system consisted of a Polymer Char (Valencia, Spain) GPC-IR high-temperature GPC chromatograph equipped with an internal IR5 infrared detector (IR5). The autosampler oven compartment was set to 160 °C, and the column compartment was set to 150 °C. The columns used were four Agilent "Mixed A" 30 cm 20-micron linear mixed-bed columns and a 20 μm precolumn. The chromatography solvent used was 1,2,4-trichlorobenzene containing 200 ppm butylated hydroxytoluene (BHT). The solvent source was nitrogen sparged. The injection volume used was 200 microliters, and the flow rate was 1.0 milliliters / minute.

[0021] The GPC column set was calibrated using 21 narrow molecular weight distribution polystyrene standards ranging from 580 to 8,400,000. The standards were prepared as six "cocktail" mixtures with at least a 10-fold separation between individual molecular weights. The standards were purchased from Agilent Technologies. The polystyrene standards were prepared at 0.025 grams in 50 milliliters of solvent for molecular weights ≥ 1,000,000 and 0.05 grams in 50 milliliters for molecular weights < 1,000,000. The polystyrene standards were dissolved at 80°C with gentle agitation for 30 minutes. A third-order polynomial was used to fit each polystyrene equivalent calibration point.

[0022] Total plate counts for the GPC column set were performed using decane (prepared at 0.04 g in 50 milliliters of TCB and dissolved for 20 minutes with gentle agitation). Plate counts (Equation 2) and symmetry (Equation 3) were determined for a 200 microliter injection according to the following equations:

number

number

[0023] Samples were prepared in a semi-automated fashion using Polymer Char's "Instrument Control" software. Samples were targeted at 2 mg / mL weight, and the solvent (containing 200 ppm BHT) was added via a Polymer Char high-temperature autosampler to a septa-capped vial pre-sparged with nitrogen. Samples were dissolved at 160°C for 2 hours with "slow" shaking.

[0024] Mn (GPC) , Mw (GPC) , and Mz (GPC) was calculated based on GPC results using Polymer Char's GPCOne™ software, the internal IR5 detector (measurement channel) of the Polymer Char GPC-IR chromatograph according to Equations 4-6 using the baseline-subtracted IR chromatogram at each equally spaced data collection point (i) and the polystyrene equivalent molecular weight obtained from the narrow standard calibration curve at point (i) from Equation 1.

number

[0025] To monitor deviations over time, a flow rate marker (decane) was introduced into each sample via a micropump controlled by a Polymer Char GPC-IR system. This flow rate marker (FM) was used to linearly calibrate the pump flow rate (flow rate (apparent)) of each sample by RV-matching the respective decane peak in the sample (RV (FM sample)) with the decane peak in the narrow standard calibration (RV (FM calibrated)). Any change in time of the decane marker peak is thus assumed to be related to a linear shift in the flow rate (flow rate (effective)) throughout the run. To facilitate the highest accuracy of the RV measurement of the flow rate marker peaks, a least-squares fitting routine is used to fit the peaks in the flow rate marker concentration chromatogram to a quadratic equation. The first derivative of the quadratic equation is then used to determine the true peak position. After calibrating the system based on the flow rate marker peaks, the effective flow rate (relative to the narrow standard calibration) is calculated as shown in Equation 7. Processing of the flow rate marker peaks is performed via Polymer Char's GPCOne™ software. For acceptable flow correction, the effective flow rate should be within ±1% of the apparent flow rate.

[0026] Flow rate (effective) = Flow rate (apparent) * (RV(FM calibrated) / RV(FM sample)) (Equation 7) Triple Detector GPC (TDGPC)

[0027] The chromatographic system, running conditions, column set, column calibration and calculation and distribution of conventional molecular weight moments were performed according to the methods described in Gel Permeation Chromatography (GPC).

[0028] For the determination of viscometer and light scattering detector offsets from the IR5 detector, a systematic approach for the determination of multiple detector offsets was performed in a manner consistent with that published by Balke, Mourey et al. (Mourey and Balke, Chromatography Polym. Chpt 12, (1992)) (Balke, Thitiratsakul, Lew, Cheung, Mourey, Chromatography Polym. Chpt 13, (1992)) using Polymer Char's GPCOne™ software to optimize triple detector log (MW and IV) results from broad, single-polymer polyethylene standards (Mw / Mn > 3) against narrow standard column calibration results from a narrow standard calibration curve.

[0029] Absolute molecular weight data were obtained using Polymer Char's GPCOne™ software in a manner consistent with that published by Zimm (Zimm, BH, J. Phys., 16, 1099 (1948)) and Kratochvil (Kratochvil, P., Classical Light Scattering from Polymer Solutions, Elsevier, Oxford, NY (1987)). The total injected concentration used in determining the molecular weight was obtained from the mass detector area and mass detector constant derived from a suitable linear polyethylene homopolymer or one of the polyethylene standards of known weight average molecular weight. Calculated molecular weights (using GPCOne™) were obtained using the light scattering constant derived from one or more of the polyethylene standards described below and a refractive index concentration coefficient (dn / dc) of 0.104. Generally, the mass detector response (IR5) and light scattering constant (determined using GPCOne™) should be determined from a linear polyethylene standard with a molecular weight of approximately 120,000 g / mol. Viscometer calibration (determined using GPCOne™) can be accomplished using methods described by the manufacturer, or alternatively, using published values ​​of suitable linear standards. A viscometer constant (obtained using GPCOne™) is calculated that relates the specific viscosity area (DV) and injected mass for the calibration standard to its intrinsic viscosity. The chromatographic concentration is assumed to be low enough to avoid the need to address second virus count effects (concentration effects on molecular weight).

[0030] Absolute weight average molecular weight (Mw (Abs) ) is obtained (using GPCOne™) by dividing the Light Scattering (LS) area integrated chromatogram (factored by the light scattering constant) by the mass recovered from the mass constant and the mass detector (IR5) area. The molecular weight and intrinsic viscosity responses are linearly extrapolated (using GPCOne™) at the chromatographic end where the signal-to-noise is low. The other respective moments, Mn (Abs) and Mz (Abs)is calculated according to the following equations 8-9:

number

number

[0031] Residual amount of catalytic metals. The "residual amount" of catalytic metals (Ti, Hf, Zr, and Ge) was 0 ppm or greater than 0 ppm to less than 300 ppm, as determined by mass balance based on the amount of catalyst added and the amount of polymer formed during the reaction. Results are reported in parts per million (ppm).

[0032] Viscosity. Viscosity was measured using an Anton Paar MCR102 equipped with a CC27 cylinder measuring system and a C-ETD300 heating system using the viscosity steady-state method at shear rates of 0.01 to 100 [1 / s]. Approximately 20 mL of sample was added to the measuring cup and then heated to 100°C. The measuring system was then lowered into the sample until it reached 0.0 mm. This was done over a period of time such that the force did not reach 15 Newtons (N). Once the measuring system reached 0.0 mm, the sample together with the measuring system were held at 100°C for 10 minutes to allow the temperature to equilibrate. The results were reported in millipascal seconds (mPas). mPa·s ) will be reported. DETAILED DESCRIPTION OF THE INVENTION

[0033] The present disclosure provides a process. In one embodiment, the process includes providing a purge stream comprising octene monomer. The process includes contacting the purge stream with a bis-biphenylphenoxy catalyst under polymerization conditions. The process provides a polymer having an absolute weight average molecular weight (Mw) of greater than 1,300,000 g / mol. (Abs) ) and Mw of 1.3 to 3.0 (Abs) / Mn (Abs) forming an octene polymer having

[0034] The process includes providing a purge stream. The purge stream comprises or otherwise contains octene monomer. As used herein, a "purge stream" is one of several fractions separated or otherwise recovered from the effluent exiting the polymerization reactor after the polymerization reaction has occurred. The liquid effluent exiting the polymerization reactor contains a solid (particulate) polymer product, which is removed. A recycle stream is also removed from the effluent, which is further processed and returned to the polymerization reactor. The purge stream is the stream remaining after (i) the polymer product has been recovered from the effluent and (ii) the recycle stream has been separated from the effluent. The purge stream contains unreacted olefin monomer and other hydrocarbons (hereinafter referred to as "hydrocarbon species") utilized during the polymerization reaction. It will be understood that the purge stream is free of, or substantially free of, solid polymer product.

[0035] In one embodiment, the purge stream is the effluent from a polymerization reactor in which ethylene is copolymerized with octene. The purge stream contains hydrocarbon species consisting of unreacted octene monomer and other hydrocarbons.

[0036] In one embodiment, the purge flow comprises: (i) 20 to 50 wt. %, or 30 to 40 wt. % of 1-octene monomer; (ii) 10% to 50% by weight, or 20% to 40% by weight, of a hydrocarbon solvent; and (iii) 10% to 70%, or 20% to 60%, or 30% to 50% by weight of octene isomers (excluding 1-octene), where the weight percentages are based on the total weight of the purge stream.

[0037] In one embodiment, the process includes removing ethylene that may be present in the purge stream. The purge stream is sparged with nitrogen gas to ensure that ethylene is not present in the purge stream. The purge stream is free or substantially free of ethylene monomer. That is, the amount of ethylene contained is from 0% by weight, or from greater than 0% by weight to less than 0.01% by weight, based on the total weight of the purge stream. The purge stream includes: (i) 20 to 50 wt. %, or 30 to 40 wt. % of 1-octene monomer; (ii) 10% to 50% by weight, or 20% to 40% by weight, of a hydrocarbon solvent; (iii) 10% to 70% by weight, or 20% to 60% by weight, or 30% to 50% by weight of octene isomers (excluding 1-octene), and (iv) zero, or substantially zero, ethylene monomer. Note that the weight percent figures are based on the total weight of the purge stream. It is understood that components (i) through (iv) add up to 100 weight percent of the purge stream.

[0038] The process involves contacting the purge stream with a bis-biphenylphenoxy catalyst under polymerization conditions. As used herein, "polymerization conditions" are the temperature, pressure, reactant concentrations, solvent selection, chain transfer agent (CTA), reactant mixing / addition parameters, and other conditions within a polymerization reactor that promote reaction between the reagents and formation of the resulting product (i.e., octene polymer or polyoctene). The polymerization can be carried out in a batch or continuous process in a tubular reactor, stirred autoclave reactor, continuous stirred tank reactor, gas-phase polymerization reactor, slurry-phase polymerization reactor, loop reactor, isothermal reactor, fluidized bed gas-phase reactor, and combinations thereof.

[0039] The purge stream is contacted under polymerization conditions with a bis-biphenylphenoxy catalyst (or interchangeably referred to as "BBP"), which is a metal-ligand complex having the structure shown in formula (I): [ka] During the ceremony, M is a metal selected from zirconium or hafnium, the metal being in the +2, +3, or +4 formal oxidation state; n is an integer of 0 to 3, and when n is 0, X does not exist; each X is independently a monodentate ligand which is neutral, monoanionic, or dianionic, or two X together form a bidentate ligand which is neutral, monoanionic, or dianionic, and X and n are selected such that the metal-ligand complex of formula (I) as a whole is neutral; Each Z is independently O, S, N (C1 to C 40 ) hydrocarbyl, or P(C1-C 40 ) hydrocarbyl, O is O (oxygen atom), L is (C1~C 40 ) hydrocarbylene or (C1-C 40 ) heterohydrocarbylene, where (C1-C 40 ) Hydrocarbylene has a moiety containing a linker skeleton of 1 to 10 carbon atoms that connects the two Z groups (to which L is attached) in formula (I), or (C1 to C 40 ) Heterohydrocarbylene has a moiety containing a linker skeleton of 1 atom to 10 atoms connecting the two Z groups in formula (I), and (C1-C 40 Each of the 1 to 10 atoms of the 1 to 10 atom linker backbone of the heterohydrocarbylene is independently a carbon atom or a heteroatom, and each heteroatom is independently O, S, S(O), S(O), Si(R C )2, Ge(R C )2, P(R C ), or N(R C ) and each R C is (C1~C 30 ) hydrocarbyl or (C1-C 30 ) heterohydrocarbyl, Each R 1~16 is (C1~C 40 ) hydrocarbyl, (C1-C 40) heterohydrocarbyl, Si(R C )3, Ge(R C )3, P(R C )2, N(R C )2, OR C , S.R. C , NO2, CN, CF3, R C S(O), R C S(O)2, (R C )2C=N,R C C(O)O, R C OC(O), R C C(O)N(R), (R C )2NC(O), a halogen atom, a hydrogen atom, and combinations thereof.

[0040] The bis-biphenylphenoxy catalyst of the structure of formula (I) can be made catalytically active by contacting the metal-ligand complex with an activating cocatalyst or by combining the metal-ligand complex with an activating cocatalyst.

[0041] Non-limiting examples of activating cocatalysts suitable for use herein include alkylaluminums, polymeric or oligomeric alumoxanes (also known as aluminoxanes), neutral Lewis acids, and non-polymeric, non-coordinating, ion-forming compounds (including the use of such compounds under oxidizing conditions). Combinations of one or more of the foregoing activating cocatalysts and techniques are also contemplated. The term "alkylaluminum" refers to monoalkylaluminum dihydrides or dihalides, dialkylaluminum hydrides or halides, or trialkylaluminums. Examples of polymeric or oligomeric alumoxanes include methylalumoxane, methylalumoxane modified with triisobutylaluminum, and isobutylalumoxane.

[0042] Non-limiting examples of Lewis acid activators (cocatalysts) include those having 1 to 3 (C1-C3) groups, as described herein. 20In one embodiment, the Group 13 metal compound includes a tri((C1-C) hydrocarbyl substituent. 20 )hydrocarbyl)-substituted aluminum, tri((C1-C 20 )hydrocarbyl)-boron compounds, tri((C1-C 10 ) alkyl) aluminum, tri((C6-C 18 )aryl)boron compounds and their halogenated (including perhalogenated) derivatives. In further embodiments, the Group 13 metal compound is tris(fluoro-substituted phenyl)borane, tris(pentafluorophenyl)borane. In some embodiments, the activating cocatalyst is tetrakis((C1-C 20 ) hydrocarbyl borate or tri((C1-C 20 )hydrocarbyl)ammonium tetrakis((C1-C 20 )hydrocarbyl)borates (e.g., bis(octadecyl)methylammonium tetrakis(pentafluorophenyl)borate). As used herein, the term "ammonium" refers to a ((C1-C 20 ) Hydrocarbyl N(H)3 + , or N(H)4 + The nitrogen cation (C1 to C 20 When two or more hydrocarbyls are present, they may be the same or different.

[0043] A non-limiting example of a combination of neutral Lewis acid activators (co-catalysts) is a tri((C1-C4) alkyl)aluminum and a tri((C6-C 18)aryl)boron compounds, particularly tris(pentafluorophenyl)borane. Other embodiments include mixtures containing such neutral Lewis acid mixtures with polymeric or oligomeric alumoxanes, and combinations of a single neutral Lewis acid, particularly tris(pentafluorophenyl)borane, with polymeric or oligomeric alumoxanes. The molar ratio of (metal-ligand complex):(tris(pentafluorophenylborane):(alumoxane) [e.g., (Group 4 metal-ligand complex):(tris(pentafluorophenylborane):(alumoxane)] is 1:1:1 to 1:10:100, and in other embodiments, 1:1:1.5 to 1:5:30.

[0044] The bis-biphenylphenoxy catalyst having the structure of formula (I) can be activated by combining it with one or more cocatalysts, such as cation-forming cocatalysts, strong Lewis acids, or combinations thereof, to form an active catalyst composition. Suitable activating cocatalysts include polymeric or oligomeric aluminoxanes, particularly methylaluminoxane, as well as inert, compatible, non-coordinating, ion-forming compounds. Exemplary suitable cocatalysts include modified methylaluminoxane (MMAO), bis(hydrogenated tallow alkyl)methyltetrakis(pentafluorophenyl)borate(1<->)amine (i.e., [HNMe(C 18 H 37 )2][B(C6F5)4] and combinations of both.

[0045] One or more of the foregoing activating cocatalysts may be used in combination with one another. In one embodiment, the cocatalyst is a mixture of tri((C1-C4)hydrocarbyl)aluminum, tri((C1-C4)hydrocarbyl)borane, or ammonium borate with an oligomeric or polymeric alumoxane compound. The ratio of the total number of moles of the one or more metal-ligand complexes of Formula (I) to the total number of moles of the one or more activating cocatalysts is 1:10,000 to 100:1. In some embodiments, this ratio is at least 1:5000; in other embodiments, it is at least 1:1000 and no more than 10:1; and in other embodiments, it is no more than 1:1. When alumoxane is used alone as the activating cocatalyst, it is preferred that the number of moles of alumoxane used be at least 100 times the number of moles of the metal-ligand complex of Formula (I). When tris(pentafluorophenyl)borane is used alone as the activating cocatalyst, in some other embodiments, the ratio of the number of moles of tris(pentafluorophenyl)borane used to the total number of moles of the one or more metal-ligand complexes of Formula (I) is from 0.5:1 to 10:1, from 1:1 to 6:1, or from 1:1 to 5:1. The remaining activating cocatalysts are generally used in a molar amount approximately equal to the total molar amount of the one or more metal-ligand complexes of Formula (I).

[0046] In one embodiment, the bis-biphenylphenoxy catalyst having the structure of Formula (I) comprises a metal M that is zirconium.

[0047] The process comprises contacting the purge stream with a bis-biphenylphenoxy catalyst of formula (I) under polymerization conditions and producing a bis-biphenylphenoxy copolymer having an absolute weight average molecular weight (Mw) of greater than 1,300,000 g / mol. (Abs) ) and Mw of 1.3 to 3.0 (Abs) / Mn (Abs) and forming an octene polymer having:

[0048] The process involves avoiding or otherwise excluding a titanium-containing catalyst and / or a titanium-containing cocatalyst from the contacting step.

[0049] In one embodiment, the bis-biphenylphenoxy catalyst is a metal-ligand complex having the following structural formula (V): [ka] where Ge is germanium, Me is a methyl group, tBu is a t-butyl group, and iPr is an isopropyl group. The process comprises contacting the purge stream under polymerization conditions with a bis-biphenylphenoxy catalyst of formula (V) and producing an octene polymer: (i) Mw of more than 1,300,000 to 12,000,000 g / mol, or 1,400,000 to 10,000,000 g / mol, or 1,400,000 to 9,000,000 g / mol, or 1,500,000 to 8,000,000 g / mol (Abs) and, (ii) Mw of 1.3 to 3.0, or 1.4 to 2.9, or 1.5 to 2.8, or 2.1 to 2.7, or 2.2 to 2.6 (Abs) / Mn (Abs) and, (iii) forming an octene polymer having a residual amount of zirconium and a residual amount of germanium.

[0050] The process involves avoiding or otherwise excluding a titanium-containing catalyst and / or a titanium-containing cocatalyst from the contacting step.

[0051] In one embodiment, the bis-biphenylphenoxy catalyst is a metal-ligand complex having the following structural formula (VI): [ka] where Me is a methyl group and tBu is a t-butyl group. The process comprises contacting the purge stream under polymerization conditions with a bis-biphenylphenoxy catalyst of formula (VI) and producing an octene polymer, (i) Mw of more than 1,300,000 to 12,000,000 g / mol, or 1,400,000 to 10,000,000 g / mol, or 1,400,000 to 9,000,000 g / mol, or 1,500,000 to 8,000,000 g / mol (Abs) and, (ii) Mw of 1.3 to 3.0, or 1.4 to 2.9, or 1.5 to 2.8, or 2.1 to 2.7, or 2.2 to 2.6 (Abs) / Mn (Abs) and, (iii) forming an octene polymer having a residual amount of zirconium.

[0052] The process involves avoiding or otherwise excluding a titanium-containing catalyst and / or a titanium-containing cocatalyst from the contacting step.

[0053] The present disclosure provides a composition. In one embodiment, a composition is provided, the composition comprising: (i) an absolute weight average molecular weight (Mw) greater than 1,300,000 g / mol; (Abs) ) and Mw of 1.3 to 3.0 (Abs) / Mn (Abs) The composition further comprises an octene homopolymer having the formula (II). The octene homopolymer contains titanium in an amount of 0 ppm or more, or more than 0 ppm and less than 10 ppm. The composition also comprises (ii) a solvent.

[0054] The octene homopolymer is dissolved in a solvent. The solvent is a linear, branched, or cyclic C4-C 14 , or C6~C 12 Aliphatic hydrocarbons. Non-limiting examples of suitable aliphatic hydrocarbon solvents include butane, pentane, hexane, heptane, octane, nonane, decane, undecane, dodecane, tridecane, tetradecane, pentadecane, hexadecane, and combinations thereof.

[0055] In one embodiment, the composition comprises an octene homopolymer dissolved in a solvent, the octene homopolymer being polymerized using a catalyst of formula (I), or formula (V), or formula (VI), wherein the octene homopolymer has one, some, or all of the following properties: (i) Mw of more than 1,300,000 to 12,000,000 g / mol, or 1,400,000 to 10,000,000 g / mol, or 1,400,000 to 9,000,000 g / mol, or 1,500,000 to 8,000,000 g / mol (Abs) and / or (ii) Mw of 1.3 to 3.0, or 1.4 to 2.9, or 1.5 to 2.8, or 2.1 to 2.7, or 2.2 to 2.6 (Abs) / Mn (Abs) and / or (iii) residual amounts of zirconium, or greater than 0 ppm, or between 1 and less than 300 ppm, or between 10 and 200 ppm, or between 15 and 180 ppm, or between 20 and 170 ppm, or between 30 and 160 ppm; and / or (iv) residual amounts of germanium, or greater than 0 ppm, or 1 to less than 300 ppm, or 10 to 200 ppm, or 12 to 150 ppm, or 14 to 130 ppm, or 14 to 125 ppm; and / or (v) Titanium from 0 ppm or more to less than 10 ppm.

[0056] In one embodiment, the composition comprises (i) 10 to 50 wt. % of an octene homopolymer, (ii) 0 to 70 wt. % of an octene isomer, and (iii) 90 to 10 wt. % of a solvent, the amounts of components (i), (ii), and (iii) combined totaling 100 wt. % of the composition.

[0057] In one embodiment, the composition comprises: (i) 10% by weight, or 20% by weight, or 30% by weight to 40% by weight, or 50% by weight of an octene homopolymer; (ii) 0 wt.%, or 10 wt.%, or 25 wt.% to 50 wt.%, or 75 wt.% of octene isomers; (iii) 90% by weight, or 80% by weight, or 70% by weight to 60% by weight, or 50% by weight of a solvent, wherein the amounts of (i), (ii), and (iii) together equal 100% by weight of the composition.

[0058] In one embodiment, the composition comprises: (i) 25 or 30% to 35% by weight of an octene homopolymer; (ii) 30 or 35 wt. % to 40, or 45, or 50 wt. % of an octene isomer; and (iii) 10 or 15% to 20 or 25% by weight of a solvent, the amounts of (i), (ii), and (iii) together totaling 100% by weight of the composition.

[0059] In one embodiment, the composition comprises from 80 or 85 wt % to 90 or 95 wt % of octene homopolymer and from 20 or 15 wt % to 10 or 5 wt % of solvent, the amounts of octene homopolymer and solvent together making up 100 wt % of the composition.

[0060] In one embodiment, the composition comprises: (i) 35 to 45 wt. % of an octene homopolymer; (ii) 65 to 55 wt. %, and the total amount of (i) and (ii) equals 100 wt. % of the composition; The composition is 2.9014*10 +05 mPa·s ~3.573*10 +07 mPa·s It has a viscosity of

[0061] By way of example, and not limitation, some embodiments of the present disclosure will now be described in detail in the following examples. [Example]

[0062] The catalysts used in the comparative samples (CS) and inventive examples (IE) are provided in Table 1 below. [Table 1] A. Polymerization Using a Purge Stream

[0063] FIG. 1 is a schematic diagram of a process for the polymerization of ethylene and octene. Ethylene monomer, octene comonomer, solvent, and catalyst are fed to a reactor. The resulting ethylene / octene copolymer is recovered, a recycle stream is reintroduced into the reactor, and a purge stream is separated from the ethylene and octene polymerization process. The purge stream contains 20-50 wt. % 1-octene, 10-70 wt. % octene isomers, and 10-50 wt. % ISOPAR-E, based on the total weight of the purge stream. ISOPAR-E is commercially available from Exxon Chemical Co. 8~12 It is an aliphatic solvent.

[0064] The purge streams used to generate either the comparative samples (CS) and the inventive examples (IE) are provided below: Purge Stream A: 45 wt. % 1-octene, 45 wt. % octene isomers, and 10% ISOPAR-E, based on the total weight of Purge Stream A; and Purge Stream B: 37 wt. % 1-octene, 46 wt. % octene isomers, and 17% ISOPAR-E, based on the total weight of Purge Stream B.

[0065] The purge stream is collected, purged with nitrogen, filtered through molecular sieves, and stored in a nitrogen-filled glove box.

[0066] For the comparative sample (CS), polymerization was carried out using Ziegler-Natta catalyst (ZN) in a 40 mL vial charged with 12 mL of purge flow, 4 μmol of catalyst (ZN), and 5 equivalents (eq) of EtAl (as an activator) at a temperature of 23–25 °C over a 12-h period. The solvent and unreacted octene isomers were then removed under vacuum. CS5 was polymerized in the same manner, except that the solution temperature was maintained at -35 °C for 48 h during the polymerization.

[0067] For the inventive examples (IE1-14), polymerizations were carried out using bis-biphenylphenoxy catalyst (either BBP1 or BBP2) with a 12 mL purge flow, 4 μmol of catalyst, and 1.2 equivalents of (RN(H)MeB(CF) (where R is hydrogenated tallow alkyl (C 14~18 The reaction is carried out in a 40 mL vial charged with octene isomers (C14-C16 alkyl) (CAS number 200644-82-2) at 23-25°C for 12 hours. The solvent and unreacted octene isomers are then removed under vacuum.

[0068] The polymerization results are reported in Table 2 below.

[0069] The properties of the resulting octene homopolymer are provided in Table 2 below. [Table 2] 1 The amount of residual catalyst metal present in the octene homopolymer (ppm), based on the total weight of the octene homopolymer. 2 The polymerization was carried out at -35°C.

[0070] Table 2 shows that polymerization of 1-octene from the purge stream using a ZN catalyst at room temperature (CS1-4) yielded polyoctenes with molecular weights ranging from 1,500,000 to 1,900,000 g / mol and broad molecular weight distributions (Mw / Mn) ranging from 6.94 to 8.97. Lowering the polymerization temperature to -35°C (CS5) resulted in significantly higher molecular weights.

[0071] When the inventive catalysts BBP1 and BBP2 were used (IE1-IE14), the molecular weight of the polyoctene was significantly higher, exceeding 1,300,000 g / mol, and in particular in the range of 1,400,000 to 8,600,000 g / mol when 1-octene was polymerized from the purge stream at room temperature. Only inventive examples IE1-IE14 were high molecular weight polyoctene (greater than 1,300,000 g / mol) obtained with a narrow molecular weight distribution (1.3 to 3.0, especially 1.42 to 2.09). The resulting high molecular weight polyoctene was titanium-free or otherwise titanium-free. Inventive examples IE1-IE14 yielded high molecular weight polyoctene containing residual zirconium, and inventive examples IE1-IE12 yielded high molecular weight polyoctene containing residual zirconium and residual germanium.

[0072] The present disclosure is not limited to the embodiments and examples contained herein, but is expressly intended to include portions of the embodiments and modified forms of those embodiments, including combinations of elements of different embodiments, to the extent that they fall within the scope of the following claims. It should be noted that the present invention includes the following aspects. [Aspect 1] providing a purge stream comprising octene monomer; contacting said purge stream with a bis-biphenylphenoxy catalyst under polymerization conditions; Absolute weight average molecular weight (Mw) greater than 1,300,000 g / mol (Abs) ) and Mw of 1.3 to 3.0 (Abs) / Mn (Abs) and forming an octene polymer having: [Aspect 2] 2. The process of embodiment 1, comprising contacting the purge stream with a bis-biphenylphenoxy catalyst represented by formula (I): [ka] (In the formula, M is a metal selected from zirconium or hafnium, said metal being in a +2, +3, or +4 formal oxidation state; n is an integer of 0 to 3, and when n is 0, X does not exist; each X is independently a monodentate ligand which is neutral, monoanionic, or dianionic, or two X together form a bidentate ligand which is neutral, monoanionic, or dianionic, and X and n are selected such that the metal-ligand complex of formula (I) as a whole is neutral; Each Z is independently O, S, N(C 1 ~C40 ) hydrocarbyl, or P(C 1 ~C 40 ) hydrocarbyl, O is O (oxygen atom), L is (C 1 ~C 40 ) hydrocarbylene or (C 1 ~C 40 ) heterohydrocarbylene, wherein said (C 1 ~C 40 ) hydrocarbylene has a moiety containing a linker skeleton of 1 to 10 carbon atoms that connects the two Z groups (to which L is attached) in formula (I), or 1 ~C 40 ) heterohydrocarbylene has a moiety containing a linker skeleton of 1 atom to 10 atoms that connects the two Z groups in formula (I), and the (C 1 ~C 40 ) Each of the 1 to 10 atoms of the 1 to 10 atom linker backbone of the heterohydrocarbylene is independently a carbon atom or a heteroatom, and each heteroatom is independently O, S, S(O), S(O) 2 , Si(R C ) 2 , Ge(R C ) 2 , P(R C ), or N(R C ) and each R C is (C 1 ~C 30 ) hydrocarbyl or (C 1 ~C 30 ) heterohydrocarbyl, Each R 1~16 is (C 1 ~C 40 ) hydrocarbyl, (C 1 ~C 40 ) heterohydrocarbyl, Si(R C ) 3 , Ge(R C ) 3 , P(R C ) 2 , N(R C ) 2 , OR C , S.R. C , NO 2 , C.N., C.F. 3 、R C S(O), R C S(O) 2、(R C ) 2 C=N, R C C(O)O, R C OC(O), R C C(O)N(R), (R C ) 2 is selected from NC(O), a halogen atom, a hydrogen atom, and a combination thereof. [Aspect 3] 20 to 50 wt. % of 1-octene; 10 to 50 wt. % of a solvent; 3. The process of any one of claims 1 to 2, comprising providing a purge stream consisting of: 10 to 70 wt. % octene isomers. [Aspect 4] removing ethylene present in said purge stream prior to said contacting; providing a purge stream comprising 0 to less than 0.01 wt. % ethylene. [Aspect 5] The process of any one of embodiments 1-4, comprising contacting the purge stream with a bis-biphenylphenoxy catalyst represented by formula (V):

change

change

Claims

1. providing a purge stream comprising octene monomer; contacting said purge stream with a bis-biphenylphenoxy catalyst under polymerization conditions; Absolute weight average molecular weight (Mw) greater than 1,300,000 g / mol （Ａｂｓ） ) and Mw of 1.3 to 3.0 （Ａｂｓ） / Mn （Ａｂｓ） and forming an octene polymer having:

2. 2. The process of claim 1, comprising contacting the purge stream with a bis-biphenylphenoxy catalyst represented by formula (I): 【Chemistry 1】 (In the formula, M is a metal selected from zirconium or hafnium, said metal being in a +2, +3, or +4 formal oxidation state; n is an integer from 0 to 3, and when n is 0, X is absent; each X is independently a monodentate ligand which is neutral, monoanionic, or dianionic, or two X together form a bidentate ligand which is neutral, monoanionic, or dianionic, and X and n are selected such that the metal-ligand complex of formula (I) as a whole is neutral; Each Z is independently O, S, N(C １ ~C ４０ ) hydrocarbyl, or P(C １ ~C ４０ ) hydrocarbyl, O is O (oxygen atom), L is (C １ ~C ４０ ) hydrocarbylene or (C １ ~C ４０ ) heterohydrocarbylene, wherein said (C １ ~C ４０ ) hydrocarbylene has a moiety containing a linker skeleton of 1 carbon atom to 10 carbon atoms connecting the two Z groups (to which L is attached) in formula (I), or １ ~C ４０ ) heterohydrocarbylene has a moiety containing a linker skeleton of 1 atom to 10 atoms connecting the two Z groups in formula (I), １ ~C ４０ ) each of the 1 to 10 atoms of the 1 to 10 atom linker backbone of the heterohydrocarbylene is independently a carbon atom or a heteroatom, and each heteroatom is independently O, S, S(O), S(O) ２ , Si(R Ｃ ) ２ , Ge(R Ｃ ) ２ , P(R Ｃ ), or N(R Ｃ ) and each R Ｃ is (C １ ~C ３０ ) hydrocarbyl or (C １ ~C ３０ ) heterohydrocarbyl, Each R １～１６ is (C １ ~C ４０ ) hydrocarbyl, (C １ ~C ４０ ) heterohydrocarbyl, Si(R Ｃ ) ３ , Ge(R Ｃ ) ３ , P(R Ｃ ) ２ , N(R Ｃ ) ２ , OR Ｃ , S.R. Ｃ , NO ２ , C.N., C.F. ３ , R Ｃ S(O), R Ｃ S (O) ２ , (R Ｃ ) ２ C=N, R Ｃ C(O)O,R Ｃ OC(O), R Ｃ C(O)N(R), (R Ｃ ) ２ NC(O), a halogen atom, a hydrogen atom, and a combination thereof.

3. 20 to 50 wt. % of 1-octene; 10 to 50 wt. % of a solvent; 3. The process of claim 1 or 2, comprising providing a purge stream consisting of: 10 to 70 wt. % octene isomers.

4. removing ethylene present in said purge stream prior to said contacting; providing a purge stream comprising 0 to less than 0.01 wt. % ethylene.

5. 5. The process of any one of claims 1 to 4, comprising contacting the purge stream with a bis-biphenylphenoxy catalyst represented by formula (V): 【Chemistry 2】

6. 5. The process of any one of claims 1 to 4, comprising contacting the purge stream with a bis-biphenylphenoxy catalyst represented by formula (VI): 【Transformation 3】

7. Absolute weight average molecular weight (Mw) of greater than 1,300,000 g / mol to 9,000,000 g / mol （Ａｂｓ） ) and Mw of 1.3 to 3.0 （Ａｂｓ） / Mn （Ａｂｓ） wherein the octene homopolymer contains a residual amount of zirconium in an amount of more than 0 ppm to less than 300 ppm and a residual amount of titanium in an amount of 0 ppm to less than 10 ppm, and the zirconium and titanium are derived from a polymerization catalyst for the octene homopolymer; A method for making a composition comprising:

8. 8. The method of claim 7, wherein the octene homopolymer contains a residual amount of germanium in an amount greater than 0 ppm and less than 300 ppm.

9. The composition comprises: (i) 10 to 50 wt. % of said octene homopolymer; (ii) 0 to 70 wt. % of an octene isomer; and (iii) 90 to 10 wt. % of said solvent, wherein the amounts of (i), (ii), and (iii) together make 100 wt. % of the composition.

10. The composition comprising: 80 to 95 wt. % of said octene homopolymer; 9. The method of claim 7 or 8, comprising: 20 to 5% by weight of said solvent.

11. The composition comprises: (i) 35 to 45 wt. % of said octene homopolymer; (ii) 65 to 55 wt. % of said solvent, wherein the amounts of (i) and (ii) together total 100 wt. % of said composition; The composition has a viscosity of 2.9014 ＊ 10 ＋０５ mPa・s~3.573 ＊ 10 ＋０７ 9. The method according to claim 7 or 8, wherein the composition has a viscosity of 0.05 to 0.15 mPa·s.

Images