Photovoltaic module backsheet comprising polyolefin layers
US-2024063320-A1 · Feb 22, 2024 · US
US2017306136A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2017306136-A1 |
| Application number | US-201715644528-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jul 7, 2017 |
| Priority date | Jun 5, 2015 |
| Publication date | Oct 26, 2017 |
| Grant date | — |
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This invention relates to heterophasic copolymers of propylene and an alpha olefin comonomer having a high fill phase content (≧15%), and heterophasic polymerization processes using a single site catalyst system with a support having high average particle size (PS≧30 μm), high surface area (SA≧400 m 2 /g), low pore volume (PV≦2 mL/g), and a mean pore diameter range of 1≦PD≦20 nm.
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1 . A process for polymerization of propylene and a comonomer, comprising: (a) contacting propylene monomer under polymerization conditions with a first catalyst system, comprising a single site catalyst precursor compound, an activator, and a support having an average particle size of more than 30 microns, a surface area of 400 m 2 /g or more, a pore volume of from 0.5 to 2 mL/g, and a mean pore diameter of from 1 to 20 nm (10 to 200 angstroms) as determined by BET nitrogen adsorption, to form a matrix phase of propylene polymer comprising at least 50 mol % propylene and having a porosity of 15% or more as determined by mercury intrusion porosimetry; and (b) contacting an alpha olefin monomer selected from ethylene, C 3 to C 20 alpha olefins, or a combination thereof, including at least one alpha olefin other than propylene, with a second catalyst system under polymerization conditions to form a fill phase for the pores of the matrix, wherein the second catalyst system comprises a metallocene catalyst precursor compound, an activator, and a support, and wherein the second catalyst system comprises, compositionally, the same or different single site catalyst precursor compound as in the first catalyst system, the same or different activator as in the first catalyst system, the same or different support as in the first catalyst system, or any combination thereof. (c) obtaining a heterophasic propylene copolymer composition comprising: A) a matrix phase comprising at least 50 mol % propylene and having: 1) a 1% Secant flexural modulus of at least 1000 MPa, determined according to ASTM D 790 (A, 1.0 mm/min); more than 5 and less than 200 regio defects (defined as the sum of 2,1-erythro and 2,1-threo insertions, and 3,1-isomerizations) per 10,000 propylene units, determined by 13 C NMR; and 3) when comonomer is present, a composition distribution breadth index of 50% or more; and B) a fill phase at least partially filling pores in the matrix phase, wherein the fill phase comprises at least 30 wt % of the heterophasic propylene copolymer composition, based on the total weight of the matrix and fill phases. 2 . The process of claim 1 , wherein the fill phase comprises 35 wt % or more of the heterophasic propylene copolymer composition, based on the total weight of the matrix and fill phases. 3 . The process of claim 1 , wherein the matrix phase has a melting point (Tm, DSC peak second melt) of at least 100° C. 4 . The process of claim 1 , wherein the matrix phase has a median pore diameter less than 165 μm, as determined by mercury intrusion porosimetry. 5 . The process claim 1 , wherein the fill phase comprises a polyolefin having a Tg of −20° C. or less determined by DSC. 6 . The process of claim 1 , wherein the matrix phase has a multimodal molecular weight distribution and an overall molecular weight distribution of 5 or more. 7 . The process of claim 1 , wherein the fill phase of component B) comprises ethylene and from about 3 wt % to 75 wt % of one or more C 3 to C 20 alpha olefins. 8 . The process of claim 1 , wherein the fill phase of component B) has a CDBI of 50% or more. 9 . The process of claim 1 , wherein the heterophasic propylene copolymer composition is particulated and at least 95% by volume of the particles has a particle size greater than about 120 μm. 10 . The process of claim 1 , the heterophasic propylene copolymer composition has: 1) a total propylene content of at least 75 wt %; 2) a total co-monomer content from about 3 wt % up to about 25 wt %; 3) a CDBI of at least 60%; 4) a fill phase content of 35 wt % or more, based on the total weight of the matrix and fill phases; 5) a matrix median pore diameter greater than 6 μm and less than 160 μm, as determined by mercury intrusion porosimetry; 6) at least 50% isotactic pentads; 7) more than 10 regio defects per 10,000 propylene units, determined by 13 C NMR; 8) a 1% Secant flexural modulus of greater than about 300 MPa; 9) a matrix phase having a melting point (Tm, DSC peak second melt) of at least 120° C.; 10) a fill phase having a Tg of −30° C. or less determined by DSC; 11) a heat of fusion (Hf, DSC second heat) of 60 J/g or more; 12) at least 95% by volume having a particle size greater than 150 μm up to 10 mm; 13) a melt flow rate (MFR, ASTM 1238, 230° C., 2.16 kg) from about 0.1 dg/min up to about 300 dg/min; and 14) an Mw (as measured by GPC-DRI) from 50,000 to 1,000,000 g/mol. 11 . A process for polymerization of propylene and a comonomer, comprising: (a) contacting propylene monomer under polymerization conditions with a first catalyst system, comprising a single site catalyst precursor compound, an activator, and a support having an average particle size of more than 30 microns, a surface area of 400 m 2 /g or more, a pore volume of from 0.5 to 2 mL/g, and a mean pore diameter of from 1 to 20 nm (10 to 200 angstroms) as determined by BET nitrogen adsorption, to form a matrix phase of propylene polymer comprising at least 50 mol % propylene and having a porosity of 15% or more as determined by mercury intrusion porosimetry; and (b) contacting an alpha olefin monomer selected from ethylene, C 3 to C 20 alpha olefins, or a combination thereof, including at least one alpha olefin other than propylene, with a second catalyst system under polymerization conditions to form a fill phase for the pores of the matrix, wherein the second catalyst system comprises a metallocene catalyst precursor compound, an activator, and a support, and wherein the second catalyst system comprises, compositionally, the same or different single site catalyst precursor compound as in the first catalyst system, the same or different activator as in the first catalyst system, the same or different support as in the first catalyst system, or any combination thereof. 12 . The process of claim 11 , wherein (1) the polymerization of the alpha olefin monomer in (b) is in the presence of the matrix phase from (a), (2) the polymerization of the propylene monomer with the first catalyst system in (a) is in the presence of the fill phase from (b), or (3) a combination thereof. 13 . The process of claim 11 , wherein the contacting in (a) comprises polymerizing the propylene monomer for a time period, A1, optionally increasing a concentration of hydrogen or other chain termination agent in the polymerization after time period A1 and polymerizing the propylene in the presence of the hydrogen or other chain transfer agent for a time period, A2, wherein a time period A equals the sum of time periods A1 and A2, and the contacting in (b) comprises polymerizing the alpha olefin monomer for a time period, B, after time period A. 14 . The process of claim 13 , wherein time period A2 is greater than zero, wherein time period A1 is at least as long as time period A2, and wherein the concentration of the hydrogen or other chain transfer agent during time period A2 is at least three times greater than the concentration of the hydrogen or other chain transfer agent in time period A1. 15 . The process of claim 13 , wherein the support of the first catalyst system has an average particle size of more than 50 μm, a surface area of less than 1000 m 2 /g, or a combination thereof. 16 . The process of claim 13 , wherein the specific surface area of the support of the first catalyst system is more than 650 m 2 /g and the mean pore diameter is less than 7 nm (70 Å). 17 . The process of claim 16 , wherein the first catalyst system has a bimodal particle size distribution, wherein a larger one of the first catalyst
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