 POLYETHYLENE CATALYED BY METALOCENE
专利摘要:
metallocene-catalyzed polyethylene a metallocene-catalyzed polyethylene resin with a multimodal distribution of molecular weight and composition, comprising from 45% by weight to 75% by weight of a low density fraction, said fraction having a density less than or equal to 918 glcm3, measured according to the iso 1183 standard test method at a temperature of 23 ° c, where the density of the polyethylene resin is 0.920-0.945 glcm3, where the om, him, of the polyethylene is 2.8 to 6 in that the melting index mi2 of polyethylene resin from 0.1 to 5 g110 min measured according to the standard test method iso 1133 condition of a temperature of 190 ° c and under a load of 2.16 kg, and where the index of distribution range of strict composition (cdbi) of polyethylene resin is less than 70%, as analyzed by tref analysis (fractionation by elution with temperature gradient). 公开号:BR112014000435B1 申请号:R112014000435-8 申请日:2012-07-06 公开日:2020-03-31 发明作者:Aurélien Vantomme；Pierre Bernard；Jacques Michel；Christopher Willocq；Armelle Sigwald 申请人:Total Research & Technology Feluy； IPC主号:
专利说明:
“POLYETHYLENE CATALYED BY METALOCHENE” FIELD OF THE INVENTION The present invention relates to a polyethylene resin with multimodal distribution of molecular weight and composition, with a greater bimodal preference. The present invention also relates to said polyethylene resin for preparing films. BACKGROUND OF THE INVENTION Polyethylene has been used in the production of various film products, such as bags and packaging. Examples of such products include carry bag applications, fertilizer bags, insulation bags, food packaging, laminating film, etc. Biaxially oriented, fused polyolefin films are generally known in the art and have been used in the production of articles, such as garbage bags, shopping bags, food wraps, and any number of articles that require the orientation of the polymer chain both in machine direction (MD) and the transversal direction (TD) of the film. Although molten films can be processed to achieve biaxial orientation, blown films are generally preferred since they generally require fewer subsequent processing steps to achieve good mechanical properties. Desirable mechanical properties include dart impact, tear resistance, both on the machine and transverse directions, tensile strength, both on the machine and transverse directions, modulus of elasticity, resistance to slow puncture etc. Optical properties that are necessary, namely transparency, are measured under brightness and fog. Adapting the properties of polyolefins, such as polyethylene, to fit a desired applicability is constantly researched. In this particular case, the goal is to have a better balance between mechanical and optical properties. Medium and high density metallocene-catalyzed polyethylene are known to have good optical properties. However, for film applications, they have mechanical properties that can still be improved, namely, dart impact, tear resistance and slow puncture resistance. On the other hand, for example, polyethylene prepared with dual catalysts in the gas phase, or with Ziegler - Natta catalysts, have good mechanical properties, but poor optical properties. Nucleating agents are needed to improve brightness and haze. However, nucleating agents 2/50 are not particularly effective for polyethylene resins. For example, for a 30% haze, a nucleating agent may not improve the haze by less than 25%. Achieving excellent mechanical properties, such as dart impact and / or resistance to slow breaking and / or tear resistance, as well as good optical properties, such as brightness and fog, is an objective of the present invention. Another objective is also to maintain good processability of the polyethylene resin compositions, that is, a high melt strength, to provide a polyethylene resin composition particularly suitable for film applications. SUMMARY OF THE INVENTION According to a first aspect, the present invention provides a metallocene-catalyzed polyethylene resin having a multimodal molecular weight distribution, comprising from 45% by weight to 75% by weight of a low density fraction, said fraction having a density less than or equal to 918 g / cm 3 , measured according to the ISO 1183 standard test method at a temperature of 23 ° C, where the density of the polyethylene resin is 0.920-0.945 g / cm 3 , where M w / M n of the polyethylene is 2.8 to 6 where the melt index MI2 of polyethylene resin of between 0.1 and 5 g / 10 min measured according to the standard test method ISO 1133 Condition D at a temperature of 190 ° C and under a load of 2.16 kg, in which the strict composition distribution amplitude index (CDBI) of polyethylene resin is less than 70%, as analyzed by TREF analysis (fractionation by elution with temperature gradient ). Preferably, the polyethylene resin comprises a fraction having a higher density than the low density fraction, wherein the ratio M w of the low density fraction / M w of the high density fraction is less than 6 and greater than that 2.5; In a second aspect, the present invention also provides a film comprising the metallocene-catalyzed polyethylene resin, according to the first aspect of the invention. In a third aspect, the present invention also provides a process for preparing a metallocene-catalyzed polyethylene resin, according to the first aspect of the invention, wherein said polyethylene resin 3/50 is prepared in at least two reactors connected in series, in the presence of a catalyst system containing metallocene. Preferably, the metallocene-containing system comprises a metallocene selected from a bis-indenyl bridged metallocene or a tetrahydrogenated bis-indenyl bridged metallocene or a mixture of both. In a fourth aspect, the present invention also provides a geo-membrane produced by extrusion of flat sheet, or by extrusion of molten sheet comprising the metallocene-catalyzed polyethylene resin, according to the first aspect of the invention. In a fifth aspect, the present invention also provides a tuft of artificial slit grass or monofilaments comprising metallocene-catalyzed polyethylene resin according to the first aspect of the invention. In the following passages, the different aspects of the invention are defined in more detail. Each aspect thus defined may be combined with any other aspect or aspects, unless expressly stated otherwise. In particular, any characteristic indicated as being preferred or advantageous can be combined with any other characteristic or characteristics indicated as being preferred or advantageous. BRIEF DESCRIPTION OF THE FIGURES Figure 1 represents a graph showing the chemical composition distribution (CCD) of the curves obtained for resin 129 with two ATREF cooling conditions (temper, 6 ° C / h). Figure 2 represents a graph showing the ATREF tempering profiles for resin 129 and 8H resin, and compared to two monomodal mPE (density 0.923 g / cm 3 and 0.934 g / cm 3 ) and bimodal PE GX4081 from Basel !. Figure 3 represents a graph showing the chemical composition distribution (CCD) of the curves obtained for resin 129 and resin 8H, and compared to two monomodal mPE (density 0.923 g / cm 3 and 0.934 g / cm 3 ) and bimodal PE Basell GX4081 with ATREF tempering. Figure 4 represents a graph representing the cumulative weight fraction as a function of SCB / 1000C of resin 129 and resin 8H, and compared to two single-mode mPE (density 0.923 g / cm 3 and 0.934 g / cm 3 ) and bimodal PE GX4081 Basell. 4/50 Figure 5 represents a graph representing the cumulative weight fraction as a function of SCB / 1000C for the low density fraction of resin 129 obtained with two ATREF cooling conditions (temper, 6 ° C / h). DETAILED DESCRIPTION OF THE INVENTION Before the present aspects of the invention are described, it should be understood that this invention is not limited to the specific materials, products, articles or processes described, as these can, of course, vary. It is also to be understood that the terminology used herein is not intended to be limiting, since the scope of the present invention will be limited only by the appended claims. As used herein, the singular forms one, one, and the include both singular and plural references unless the context clearly indicates otherwise. By way of example, a polyolefin ”means a polyolefin or more than one polyolefin. The terms comprising, comprises and constituted by, as used herein, is synonymous with including, includes or containing, contains, and is inclusive or open and does not exclude additional, unquoted members, elements or stages of the method. It will be appreciated that the terms comprising, comprising and consisting of, as used herein include the terms consisting of, consists and consists of ”. The recitation of numeric ranges by periods includes all integers and, where appropriate, the fractions subsumed within that range (for example 1 to 5 may include 1,2, 3, 4 when referring to, for example, a certain number elements, and may also include 1.5, 2, 2.75 and 3.80, when referring to, for example, measurements). The repetition of the end points also includes the end point of the values themselves (for example, 1.0 to 5.0 includes both 1.0 and 5.0). Any numerical range recited here is intended to include all the sub-ranges included therein. All references cited in the present specification are hereby incorporated by reference in their entirety. In particular, the teachings of all references referred to herein are expressly incorporated by reference. According to the first aspect of the invention, a metallocene-catalyzed polyethylene resin is provided with a multimodal distribution of molecular weight and composition, said metallocene-catalyzed polyethylene resin, comprising from 45% by weight to 75% by weight of a low density fraction, said fraction having a density less than or equal to 918 g / cm 3 , for 5/50 example, less than or equal to 916 g / cm 3 , preferably less than or equal to 915 g / cm 3 , preferably less than or equal to 914 g / cm 3 , measured according to the ISO 1183 standard test method, to a temperature of 23 ° C, where the density of the polyethylene resin is 0.920-0.945 g / cm 3 , preferably 0.920-0.940 g / cm 3 , more preferably 0.920-0.936 g / cm 3 ; wherein the M w / M n of the polyethylene is 2.8 to 6.0, preferably 3.0-6.0, preferably 3.0 to 5.0, preferably 3.0-4.0, more preferably between 3.5 and 4.0; wherein the MI2 melt index of polyethylene resin is 0.1 to 5.0 g / 10 min, preferably 0.2-2.0 g / 10 min; as measured according to the ISO 1133 standard test method Condition D at a temperature of 190 ° C and under a load of 2.16 kg; and where the strict composition distribution amplitude index (CDBI) of polyethylene resin is less than 70%, as analyzed by TREF analysis (fractionation by elution with temperature gradient). As used herein, the terms metallocene-catalyzed polyethylene resin, metallocene-catalyzed polyethylene and polyethylene resin composition are synonymous and used interchangeably and refer to a polyethylene produced in the presence of a metallocene catalyst. Preferably, the metallocene-catalyzed polyethylene resin comprises from 50% by weight to 75% by weight of the low density fraction, preferably from 55% to 75% by weight of the low density fraction, based on the total weight of the resin. polyethylene. In a preferred embodiment, the molecular weight of the low density polyethylene fraction is 80-180 kDa. In a preferred embodiment, the CDBI of the low density polyethylene fraction is greater than 80%, preferably greater than 85%, more preferably greater than 90%, as analyzed by TREF under slow cooling conditions (cooling speed of 6 ° C / hour) (also referred to here as classic ATREF). The low density polyethylene fraction can be obtained from metallocene-catalyzed polyethylene resin by fractionating the resin into two fractions with preparative TREF. In one embodiment, the strict composition distribution amplitude index (CDBI) of the polyethylene resin is less than 70%, as analyzed by TREF quench analysis. 6/50 In one embodiment, the strict composition distribution amplitude index (CDBI) of the polyethylene resin is at least 30%, as analyzed by TREF quench analysis, preferably at least 35%. In a preferred embodiment, the strict composition distribution amplitude index (CDBI) of polyethylene resin is less than 70% and greater than 30%, as analyzed by TREF quench analysis. In a preferred embodiment, the polyethylene resin comprises a fraction having a higher density than the low density fraction, wherein the ratio M w of the low density fraction / M w of the high density fraction is less than 6 , 0 and greater than 2.5. For example, the M w ratio of the low density fraction / M w of the high density fraction can be less than 6.0 and greater than 2.6, for example, the M w ratio of the low density fraction / M w of the fraction high density can be less than 5.50 and greater than 2.60, for example, less than 5.30 and greater than 2.70. Preferably, the metallocene-catalyzed polyethylene resin has a polydispersity index (PI) of at least 6.5, for example, at least 6.7, for example, at least 6.9, for example at least 7.0. Preferably, the metallocene-catalyzed polyethylene resin has a fat content of less than 0.90, for example, less than 0.85, for example, less than 0.80, for example, less than 0.75. Preferably, the metallocene-catalyzed polyethylene resin has a fat content of greater than 0.35. In one embodiment, the present invention also encompasses a polyethylene resin composition with: - A molecular weight distribution with an M w / M n of 2.8 to 6, preferably 3 to 6, preferably the appearance of the molecular weight distribution curve has the appearance of a monomodal distribution: a single peak and no shoulder visible on the distribution curve; - A density of 0.920-0.945, for example 0.928-0.940 g / cm 3 measured according to the ISO 1183 standard test method at a temperature of 23 ° C; suitable for preparing a film having at least one, preferably two, more preferably all three, of the following mechanical properties: 7/50 - A dart impact (g / pm) measured according to ISO 7765-1, at least equal to the value expressed by the following equation (equation expresses the observed increase in dart impact for the film according to the invention, as density decrease); Dart> 1.4 * 22.9 2 01 + ---------------- (rf-0.918! 5> / | _ | _ e /0.004119 where d is the density in g / cm 3 measured according to ISO 1183, at a temperature of 23 ° C, - An Elmendorf tear resistance (N / mm) in the machine direction, measured according to ASTM D 1922, which is greater than or equal to the value expressed by the following equation (equation expresses tear in the machine direction as a function of the density of) : TearM> 1.3 * (11 5 / λ -) * tan ^^ 0-9-736) ^ θ_θ 0453322 ^ -0.5 * .tJ which d is the density in g / cm 3 measured according to ISO 1183, at a temperature of 23 ° C, and where the atan argument is expressed in radians; - A resistance to slow puncture of at least 65 J / mm, measured according to ASTM D5748; and at least one, preferably two, of the following optical properties: - A brightness of at least 40% measured according to ASTM D - 2457 with an angle of 45 °; - A turbidity of less than 20% measured according to the standard ISO 14782; wherein both mechanical and optical properties are measured in 40 pm blown film thickness prepared with said polyethylene resin composition using a blown film line equipment having a neck in the configuration with an extrusion thread diameter of 45mm, a length-to-diameter ratio of 30, a 120 mm diameter die, and a blowing ratio (BUR) of 2.5, a die opening of 1.4 mm, a freezing line height of 320 mm , and the cooling air to a temperature of 20 ° C. The terms in parentheses for the Dart equation express the dart impact as a function of density for the series of monomodal polyethylene films catalyzed by metallocenes. There is an improvement of at least 8/50 minus 40% with respect to metallocene-catalyzed modomodal polyethylene resin compositions for the density range covered by the invention. As an example, for a density of 0.934 g / cm 3 , a dart impact resistance may be at least 3.5 g / pm and at 0.930 g / m 3 the dart impact force may be above 4 , 5 g / pm measured according to ISO 7765-1. For the Elmendorf tear strength, the expression in parentheses of the equation describes the increased tear resistance in the machine direction as a function of density, compared to monomodal metallocene-catalyzed polyethylene resins. There is an improvement of at least 35% of the Elmendorf tear resistance for the resins according to the invention. As an example, for a density of 0.934 g / cm 3 , an Elmendorf tear resistance in the machine direction is at least 30 N / mm, measured according to ASTM D 1922; In one embodiment, the composition is suitable for preparing a film having: - A dart impact force (g / pm) of at least 1.4 * 2.01 + 22.9 {d -0.91815) / l_ | _ e /0.004119 - Elmendorf tear resistance (N / mm) in the machine direction of at least 1.3 * (115 / π} * ia tan ^ 0.92736), / θ θθ 453322 | j + 0.5 * π and at least one, preferably two, of the following optical properties: - A brightness of at least 40% measured according to ASTM D - 2457 with an angle of 45 °; - A turbidity of less than 20% measured according to the standard ISO 14782. In another embodiment, the composition is suitable for preparing a film having: - A dart impact force (g / pm) of at least 22.9 1.4 * 2.01 + (d-0.91815) / l + e /0.004119 9/50 - A resistance to slow puncture of at least 65 J / mm, measured according to ASTM D5748. and at least one, preferably two, of the following optical properties: - A brightness of at least 40% measured according to ASTM D - 2457 with an angle of 45 °; - A turbidity of less than 20% measured according to the standard ISO 14782 In yet another embodiment, the composition is suitable for preparing a film having: - Elmendorf tear resistance (N / mm) in the machine direction 1.3 * of at least tan (d -0.92736) / /(-0.00453322) + 0.5 * λ - - A resistance to slow puncture of at least 65 J / mm, measured according to ASTM D5748. and at least one, preferably two, of the following optical properties: - A brightness of at least 40% measured according to ASTM D - 2457 with an angle of 45 °; - A turbidity of less than 20% measured according to the standard ISO 14782 Preferably, the composition has an MI2 melt index of 0.1 to 5 g / 10 minutes, measured according to the ISO 1133 condition D standard test method at a temperature of 190 ° C. More preferably, the blown film compositions have an MI2 of 0.2-3.8 g / 10 min, preferably 0.2 to 3 g / 10 min. In one embodiment, the present invention also encompasses a process for preparing the polyethylene resin composition according to the invention, which comprises - a polyethylene fraction A, in a 35 to 45 weight percentage of the polyethylene resin composition, having a melting index of 1.0200 g / 10 minutes and a density of 0.920-0.965 g / cm 3 ; and a fraction B of polyethylene, in a weight percentage between 45 and 75, preferably 55 to 65 of the polyethylene resin composition, having a melting index of 0.01 to 1 g / 10 min and a density of 0.910- 0.918 g / cm 3 , where each fraction is prepared in a reactor other than at least two reactors connected in series, in the presence of a catalyst system 10/50 containing metallocene, preferably said metallocene-containing catalyst system comprising a metallocene selected from a bisindenyl bridged metallocene, a tetrahydrogenated bis-indenyl bridged metallocene or a mixture of both, the polyethylene resin composition having a density from 0.920 to 0.945g / cm 3 , for example 0.928-0.940 g / cm 3 , for example, 0.930-0.936 g / cm 3 , measured according to the ISO 1183 standard test method at a temperature of 23 ° C, a molecular weight distribution, with an M w / M n of 2.8 to 6, preferably 3 to 6, and preferably an MI2 melt index of 0.1 to 5 g / 10 min, preferably 0, 2-4 g / 10 minutes, measured following the ISO 1133 condition D standard test method at a temperature of 190 ° C. The metallocene can be selected from formulas (I) and (II) below. In particular, the invention covers films prepared from this polyethylene resin composition. Preferably, the polyethylene resin composition is a polyethylene resin composition with a molecular weight distribution, i.e., bimodal consisting essentially of polyethylene fractions A and B. Preferably, the metallocene comprises an unsubstituted bis (tetrahydroindenyl) bridge such as ethylene-bis (tetrahydroindenyl) zirconium dichloride and ethylene-bis (tetrahydroindenyl) zirconium difluoride. Preferably, the two reactors in series are two loop reactors, more preferably two suspended loop reactors or two liquid-filled loop reactors, that is, a liquid-filled double loop reactor. Preferably, polyethylene fraction A is produced in the first reactor and polyethylene fraction B is produced in the second reactor. Preferably, the polyethylene fraction A is not degassed. In an alternative embodiment, said polyethylene fraction B is produced in the first reactor and said polyethylene fraction A is produced in the second reactor. Preferably, polyethylene fraction B is degassed, such that fraction A produced in the second reactor is substantially free of comonomer, particularly for polyethylene densities of a fraction greater than 0.960 g / cm 3 . The same conditions and properties of polyethylene resin composition apply to the process for the production of resin. The present invention also encompasses a film that essentially comprises or consists of a polyethylene resin catalyzed by 11/50 metallocene having a multimodal molecular weight distribution, said resin comprises from 45% by weight to 75% by weight of a low density fraction, said fraction having a density less than or equal to 918 g / cm 3 , measured according to the ISO 1183 standard test method at a temperature of 23 ° C, where the density of the polyethylene resin is 0.920-0.945 g / cm 3 , where the M w / M n of the polyethylene is 2.8 to 6 where the melting index MI2 of polyethylene resin between 0.1 and 5 g / 10 min measured according to the standard test method ISO 1133 Condition D at a temperature of 190 ° C and under a load of 2.16 kg, and in which the strict composition distribution amplitude index (CDBI) of polyethylene resin is less than 70%, as analyzed by TREF analysis (fractionation by elution with temperature gradient). In one embodiment, the invention also encompasses the film which essentially comprises or consists of the polyethylene resin composition in which the film has at least one, preferably two, more preferably all three, of the following mechanical properties: - A dart impact force (g / pm) of at least 1.4 * 2.01 + 22.9 M-0.91815) / /11.004119 with dart to be measured according to ISO 7765-1. - Elmendorf tear resistance (N / mm) in the machine direction of at least 1.3 * (115 / j) * α tan 0-0.92736) / /(-0.00453322) + 0.5 * π tear being measured according to ASTM D 1922. - A resistance to slow puncture of at least 65 J / mm, measured according to ASTM D5748 and at least one, preferably two, of the following optical properties: - A brightness of at least 40% measured according to ASTM D - 2457 with an angle of 45 °; - A turbidity of less than 20% measured according to the standard ISO 14782 12/50 in which both mechanical and optical properties are measured in 40 pm blown film thickness prepared with said polyethylene resin composition using a blown film line equipment with a neck in the configuration with an extrusion thread diameter 45mm, a screw length-to-diameter ratio of 30, a 120 mm diameter die, and a blowing ratio (BUR) of 2.5, a 1.4 mm die opening, a freezing line height 320 mm, and the cooling air to a temperature of 20 ° C. In one embodiment, the film has: - A dart impact force (g / pm) of at least 1.4 * 22.9 + (<7-0.91815) / l_ | _ e /0.004119 measured in accordance with ISO 7765-1 and - An Elmendorf tear resistance (N / mm) in the machine direction of at least (115 / ^ -) * fatan ^ / '(í 0.00453322)) + 0.5 *' T measured according to ASTM D 1922. and at least one, preferably two, of the following optical properties: - A brightness of at least 40% measured according to ASTM D - 2457 with an angle of 45 °; - A turbidity of less than 20% measured according to ISO 14782 In another embodiment, the film may have: - A darts impact force of at least 1.4 * 22.93Ό1 + (d-0.91815) //0.004119 measured according to ISO 7765-1 and optionally - A resistance to slow puncture of at least 65 J / mm, measured according to ASTM D5748. and at least one, preferably two, of the following optical properties: - A brightness of at least 40% measured according to ASTM D - 2457 with an angle of 45 °; 13/50 - A turbidity of less than 20% measured according to the standard ISO 14782 In yet another embodiment, the film has: - Elmendorf tear resistance (N / mm) in the machine direction of at least tan (J-0.92736) / / (- 0.00453322) + 0.5 * .τ measured according to ASTM D 1922 and - A resistance to slow puncture of at least 65 J / mm, measured according to ASTM D5748. and at least one, preferably two, of the following optical properties: - A brightness of at least 40% measured according to ASTM D - 2457 with an angle of 45 °; - A turbidity of less than 20% measured according to the standard ISO 14782 The film may be a cast or blown film. The invention also covers the process for preparing the films. The same conditions apply and the properties as for the composition of the polyethylene resin. Finally, the invention also encompasses the use of the polyethylene resin composition according to the invention to prepare films, in particular fused films and blown films. The term multimodal refers to the multimodal molecular weight distribution of a polyethylene resin, which has two or more distinct populations but possibly overlapping polyethylene macromolecules each with different average molecular weights. A bimodal polyethylene will have two fractions of polyethylene A and B. The bimodal polyethylene resin composition in the present invention preferably has an apparent monomodal molecular weight distribution, which is a molecular weight distribution curve, with a single peak and not shoulder. The composition of polyethylene resin, preferably obtained by mixing at the level of polyethylene particles in which different polyethylene fractions can be obtained by using two reactors, under different polymerization conditions and transferring the first fraction to the second reactor, or that is, the reactors are connected in series. The two reactors can be operated in the comonomer / hydrogen mode of reverse configuration (also described here as 14/50 reverse), in which a first fraction of low molecular weight (high melt index), high density polyethylene is produced in the first reactor and a second fraction of high molecular weight (low melt index), of polyethylene low density is produced in the second reactor. In this case, the first fraction of polyethylene does not need to be degassed before being transferred to the second reactor. Polyethylene fraction A is preferably substantially free of comonomer, particularly for densities of a fraction A of at least 0.960 g / cm 3 . This is in opposition to the direct configuration, in which the first high molecular weight, low density polyethylene fraction B is produced in the first reactor and the second low molecular weight A fraction, high density polyethylene is produced in the second reactor, wherein in this case, the first fraction B of polyethylene, is preferably degassed, in order to remove substantially all unpolymerized comonomer and thus for said second fraction A to be substantially free of comonomer, particularly for densities of a fraction A of at least 0.960 g / cm 3 . The polyethylene resin composition according to the invention is prepared in the presence of a catalyst system containing metallocene. The metallocene comprises a bridged bis-indenyl and / or a bridged tetrahydrogenated bis-indenyl catalyst component. The metallocene is selected from one of the following formulas (I) or (II): 15/50 where each R is the same or different and is independently selected from hydrogen or XR'v where X is chosen from Group 14 of the Periodic Table (preferably carbon), oxygen or nitrogen and each R 'is the same or different and is chosen from hydrogen or a hydrocarbil of 1 to 20 carbon atoms and v +1 is the valence of X, preferably, R is a hydrogen atom, methyl, ethyl, n - propyl, iso - propyl, n - butyl, tert-butyl group; R is a structural bridge between the two indenyls or tetrahydrogenated indenyls to confer stereo rigidity comprising a C1-C4 alkylene radical, a dialkyl germanium, silicon or siloxane, or an alkylphosphine or amine radical, Q is a hydrocarbyl radical having from 1 to 20 carbon or halogen atoms, preferably Q is F, Cl or Br, and M is a transition metal in Group 4 of the Periodic Table or vanadium. Each indenyl or indenyl tetrahydro component can be substituted with R, in the same way or differently from each other in one or more positions of any of the fused rings. Each substituent is chosen independently. If the cyclopentadienyl ring is substituted, its substituent groups should not be so bulky, so as to affect the coordination of the olefin monomer to the metal M. Any XR'v substituents on the cyclopentadienyl ring are preferably methyl. More preferably, at least one, and more preferably both, the cyclopentadienyl rings are not substituted. In a particularly preferred embodiment, the metallocene comprises an unsubstituted bridged bis - indenyl and / or tetrahydrogenated bis indenyl, ie all R groups are hydrogen. More preferably, the metallocene comprises a bridged bis-tetrahydrogenated indenyl. More preferably, the metallocene is ethylene bis (tetrahydroindenyl) zirconium dichloride or ethylene bis (tetrahydroindenyl) zirconium difluoride. Metallocenes give polyethylene a very high regular incorporation over all chain lengths, therefore the 16/50 comonomer distribution is quite narrow ie the low density fraction strict composition distribution (CDB!) Index is preferably above 50%, more preferably above 70%, preferably above 75%, even more preferably greater than 80%. This can be measured by TREF analysis. The active catalyst system used for the polymerization of ethylene comprises the catalyst component described above and a suitable activating agent that has an ionizing action. Suitable activating agents are well known in the art: they include aluminum alkyl aluminoxane or boron-based compounds. Preferably, the activating agent is selected from alkyl aluminum, more preferably from one or more of TIBAL, TEAL or TNOAL More preferably, the activating agent is TIBAL. Optionally, the catalyst component can be supported on a support. Preferably, the support is silica, modified silica alumina, a modified silica, for example, MAO modified silica or a fluorinated silica support. The polymerization of high density polyethylene produced with metallocene can be carried out in gases, solution or in the suspension phase. Suspension polymerization is preferably used to prepare the polyethylene resin composition, preferably in a sludge loop reactor or in a continuously agitated reactor. The polymerization temperature ranges from 20 to 125 ° C, preferably 55-105 ° C, more preferably from 60 to 100 ° C and more preferably 65-98 ° C and the pressure ranges between 0.1 and 10 MPa, from preferably 1 to 6 MPa, more preferably 2-4.5 MPa, for a period of between 10 minutes to 6 hours, preferably 1 to 3 hours, more preferably 1 to 2.5 hours. A double loop reactor is preferably used to carry out the polymerization. More preferably, the two reactors in series are preferably a sludge or double reactor filled with circular liquid in which each mesh is operated under different conditions in order to produce the polyethylene resin composition. As described above, the dual circuit reactor can be operated with the reverse configuration or the direct configuration. In one embodiment, the low melt index, low density fraction (fraction B) has a density of at least 0.910 g / cm 3 , of 17/50 preferably at least 0.912 g / cm 3 and at most 0.918 g / cm 3 , more preferably at most 0.916 g / cm 3 , even more preferably at most 0.914 g / cm 3 . More preferably, it is about 0.915-0.918 g / cm 3 . Fraction B has an Ml melt index of at least 0.01 g / 10 min, preferably at least 0.05 g / 10 min, more preferably at least 0.1 g / 10 min, and even more preferably at least 0.2 g / 10 min and at most 1 g / 10 min, more preferably at most 0.8 g / 10 min, even more preferably at most 0.6 g / 10 min . More preferably, the M1 is 0.2 to 0.5 g / 10 min. The polyethylene fraction B, is present in a weight percentage between 45 and 75, preferably 55 to 65 of the polyethylene resin composition, preferably 5763, more preferably 58-62. The density of the high density fraction (A) is linked to that of the low density fraction (B) through the following expression: d = W A * d A + ( -W A ) * d B where W A represents the fraction by weight of fraction A, d A is the density of fraction A, d B is the density of fraction B, and in that the sum of both fractions A and B, by weight, (W A + W B ) is 1. In one embodiment, the high density fraction (A) has a low molecular weight. In one embodiment, the high melt index, highest density fraction (fraction A) has a density of at least 0.920g / cm 3 , at least 0.927g / cm 3 , preferably at least 0.930g / cm 3 , for example, at least 0.940 g / cm 3 , more preferably at least 0.942 g / cm 3 · even more preferably at least 0.945 g / cm 3 and at most 0.965 g / cm 3 , more preferably at most 0.962 g / cm 3 and even more preferably at most 0.960. More preferably, it is about 0.927-0.958 g / cm 3 . Fraction A has an Ml melt index of at least 0.5 g / 10 min, preferably at least 0.8 g / 10 min, more preferably at least 1 g / 10 min, even more preferably at least 5 g / 10 min and more preferably at least 10 g / 10 min and at most 200 g / 10 min, more preferably at most 155 g / 10 min, even more preferably at most 100 g / 10 min. More preferably, the M1 is 0.8-100 g / 10 minutes. Polyethylene fraction A is present in a 35 to 45 weight percent of the polyethylene resin composition, preferably 37-43, more preferably 38-42. The melt index and fraction density in the second reactor was determined using the following formula: 18/50 μM / final = wt% 1stx LogMIlst + iví% 2nd x LogM12nü density ^ = wt% 1st x density 1st + wt% 2nd x density 2nd where - final meaning polyethylene resin - 1st means the fraction of polyethylene produced in the first reactor - 2nd means the fraction of polyethylene produced in the second reactor, downstream from the first reactor. The weight average molecular weight (M w ) of the second fraction (B) can be determined using the following formula: M w B = (M w - W A * M wA ) / (1 - W A ), based on the additive rule for mixtures of miscible polyethylene of similar molecular weight distribution (for example, in the present case, D ( Mw / Mn) can be between 2.3 and 2.7), with M w being the M w of the final resin. M w = W A * M wA + (1 -W a ) * MW b This mixing rule is as described in LA Utracki and B. Schlund in Polym. Eng. I know. 27, 1512 (1987). The average number of molecular weight M r of fraction B can be calculated from M we by dividing the value by 2.6. The polyethylene resin composition according to the invention has a density of 0.920-0.945 g / cm 3 , for example, 928-0.940 g / cm 3 , preferably 0.930-0.938 g / cm 3 , more preferably 0.932-0.936 g / cm 3 , more preferably 0.932-0.934 g / cm 3 . The type and amount of comonomers used to prepare the copolymers useful with the invention will determine the density of the copolymer. Examples of comonomers that can be used to prepare the resin composition of the invention include alpha-olefins having 3 to 12 carbon atoms, in particular propylene, butene, hexene and octene. Preferably hexene is used. A person skilled in the art of preparing copolymers will know how to vary the monomer feed for any specific production unit to achieve a specified density. The polyethylene resin composition preferably has an MI2 melting index from 0.1 to 5, from 0.1 to 4 g / 10 minutes, preferably from 0.2 to 4.0 g / 10 min, even more preferably 0.3 to 3.0 g / 10 min, following the standard test method ISO 1133 condition D at a temperature of 190 ° C. These are ranges for polyethylene resin compositions particularly suitable for film applications. 19/50 More particularly, tubular film compositions have an MI2 of 0.1-4 g / 10 minutes, more preferably 0.1 to 3.0 g / 10 min. More preferably, the fused film compositions have an MI2 of 2.5 to 5 g / 10 min, more preferably 2.5 to 4.0 g / 10 min. The polyethylene resin composition of the present invention preferably has a multimodal, preferably a bimodal molecular weight distribution, with an apparent monomodal molecular weight distribution, which is a molecular weight distribution curve, with a single peak and not shoulder. The polyethylene resin composition has an extended molecular weight distribution curve due to the bimodal molecular weight composition. In a preferred embodiment, the polyethylene resin compositions of the present invention are bimodal in the composition as measured by TREF analysis. TREF analysis can be performed as described in Wild et al. J. Poli. Sci., Poly. Phys. Ed. Vol. 20, (1982), 441 or U.S. Patent No. 5,008,204). TREE profiles were obtained in analytical mode (ATREF) using two cooling conditions: tempering and 6 ° C / h (classic ATREF). TREF was also operated in the preparative mode (PTREF) to obtain low density and higher density fractions. TREF analysis can be performed with the polymer TREE instrument by CHAR (Valencia, Spain). TREF profiles can be obtained using the following conditions: ATREF cooling (analytical TREF): dissolution in 1,2,4 - trichlorobenzene (TCB) at 160 ° C for 1 h, detector (DRI differential retraction index), injection of the solution in the ATREF column at about 30 ° C. Heating rate from 2 ° C / min to 130 ° C. Concentration of 0.05% by weight. Classic ATREF: a 0.05 wt% polyethylene solution was prepared as described for the 160 ° C quenching TREF and was injected into the ATREF column and allowed to cool slowly (to 6 ° C / h) between 100 and 30 ° C. In order to calibrate the elution temperature with SCB (short chain branching) (determined by NMR), samples of known SCB and narrow distribution of comonomer composition (with CDBI> 90%) were analyzed using TREE and this allowed to derive a T elution -SCB calibration curve. Using the cumulative PE elution distribution curve as a function of SCB, the CDBI (strict composition distribution amplitude index) was calculated as taught in WO 93/03093 p. 18-19 and in Figure 17. The clear distinction between low density species (fraction with density <0.918 g / cm 3 ) and species of 20/50 higher density were seen with a marked bimodal character of the SCB distribution profile. Preferably, the strict composition distribution amplitude index (CDBI) of polyethylene resin is less than 70%, preferably below 68%, as analyzed by TREF quenching, and the CDBI of the low density polyethylene fraction is greater than 70%, preferably greater than 75%, more preferably greater than 80%, as analyzed by TREE. The w / M n of the composition is 2.8 to 6, for example 3 to 6, preferably 2.8-5.5, more preferably 2.9-5.0, more preferably 2.9-4, 6, even more preferably 3.0-4.5. The density is measured according to the ISO 1183 standard, at a temperature of 23 ° C. The MI2 melt index and high load HLMI melt index are measured by the ISO 1133 Condition D standard test method, respectively, under a load of 2.16 kg and 21.6 kg and at a temperature of 190 ° C. The molecular weight distribution is defined by the ratio M w / M n of the average molecular weight M w the average molecular weight in number M n , as determined by gel permeation chromatography (GPC). The polyethylene resin composition according to the invention has particular rheological properties. The resins according to the invention exhibit an increase in the zero cut viscosity. The increase in zero-cut viscosity is linked to agheo which is a quantification of the amount of long chain branching (LCB) as probed by rheological techniques. g rheo can be determined according to the disclosure, in WO 2008/113680: M ^ SEC) Mjr ^ MWD'SCB) where M w (SEC) is the average molecular weight obtained from size exclusion chromatography, expressed in kDa, as described above, and where M w (η 0 , MWD, SCB) is determined according to the following: Μ η . (Η 0 , MWD, SCB) = exp (1.7789 + 0.199769 LnM tl + 0.209026 (Ln) + 0.955 (ln p) - 0.00756 i (LnM.) (Ln) + 0.02355 (In WH 21/50 P density is measured in g / cm3 and measured according to ISO 1183, at a temperature of 23 ° C, Zero shear viscosity η 0 in Pa.s is obtained from a frequency sweep experiment combined with a creep test, in order to extend the frequency range of displacement values of 10 4 s 1 or less, and having the usual assumption of equivalence of angular frequency (rad / s) and shear rate. Zero shear viscosity q 0 is estimated by fitting with Carreau - Yasuda flow curve (η - W), at a temperature of 190 ° C, obtained by oscillatory shear rheology in ARES - G2 equipment (manufactured by TA Instruments) in the domain of linear viscoelasticity. Circular frequency (W in rad / s) ranges from 0.05-0.1 rad / s to 250-500 rad / s, typically 0.1-250 rad / s, and the shear strain is typically 10%. In practice, the creep experiment is carried out at a temperature of 190 ° C under a nitrogen atmosphere, with a stress level such that after 1200 s the total deformation is less than 20%. The device used is an AR - G2 manufactured by TA Instruments. PI (polydispersity index) determined by rheological methods provides a second measurement of polydispersity molecular weight. polydispersity index (PI) was determined at a temperature of 190 ° C using parallel ARES G2 rheometer plates marketed by the TA instrument (USA), operating at an oscillation frequency that increases from 0.1 rad / sec to about 300 rad / s. From the passage module, PI can be derived by means of the equation: PI = 106 / Gc where Gc is the crossing module, which is defined as the value (expressed in Pa) where G '= G, in that G is the storage module and G is the loss module. The polyethylene resin compositions according to the invention also have good processability and high melt strength. Melting resistance increases as MI2 decreases and as fat decreases. In one embodiment, the polyethylene resins of the invention have a grease below 0.9, and have greater resistance to melting than other bimodal resins with gas close to 1 (linear PE). Improved processability of the resins of the invention can also be identified by the high SR ratio (HLMI / MI2) which reflects the increased thinning behavior by cutting the resins present. Both high PI values and low gr heo contribute to an advanced shear thinning behavior. This processing can also be measured for the resins of the present invention, in part, by its ability to be 22/50 processed at an extrusion pressure relatively comparable to the MI2 value, despite its high molecular weight. Desirably, the polyethylene resin compositions have sufficient melt strength to allow processing at the applicable extrusion pressures. The polyethylene resin composition of the present invention can contain additives, in particular, additives suitable for injection blow molding, such as, for example, processing aids, release agents, anti-slip agents, primary and secondary oxidants, light stabilizers, anti-UV agents, acid scavengers, flame retardants, fillers, nanocomposites, lubricants, anti-static, nucleating / clarifying additives, antibacterial agents, plasticizers, dyes / pigments / dyes and their mixtures. Illustrative pigments or dyes include titanium dioxide, carbon black, cobalt oxides, aluminum, such as cobalt blue and chromium oxides, such as chromium oxide green. Pigments such as ultramarine blue, blue phthalocyanine and red iron oxide are also suitable. Specific examples of additives include lubricants and mold release agents such as calcium stearate, zinc stearate, SHT, antioxidants such as Irgafos 168 ™, Irganox 1010 ™, and Irganox 1076 ™, anti-slip agents, such as erucamide , light stabilizers, such as Tinuvin 622 ™ and Tinuvin 326 ™, and agents such as Milliken HPN20E ™ nucleation. An overview of the additives that can be used in the stretch blow injection of molded articles of the present invention can be found in Plastics Additives Handbook, ed. H. Zweifel, 5th edition, 2001, Hanser Publishers. FILM APPLICATIONS The polyethylene resin composition according to the invention is particularly suitable for film applications, that is, for preparing films. In particular, it provides a good balance in both mechanical and optical properties. Compared to commercial grades, the mechanical properties are as good, if not better, with the advantage that the films obtained with this metallocene-catalyzed polyethylene are particularly transparent, that is, low fog. Accordingly, the present invention also encompasses a film comprising the metallocene-catalyzed polyethylene resin according to the first aspect of the invention. 23/50 Accordingly, the present invention also relates to a film comprising a metallocene-catalyzed polyethylene resin, said resin having a multimodal molecular weight distribution, wherein said resin comprises from 45% by weight to 75% by weight of a low density fraction, said fraction having a density less than or equal to 918 g / cm 3 , measured according to the ISO 1183 standard test method at a temperature of 23 ° C; wherein the density of the polyethylene resin is 0.920-0.945 g / cm 3 ; where the M w / M n of the polyethylene is 2.8 to 6; where the MI2 melting index of polyethylene resin between 0.1 and 5 g / 10 minutes, measured according to the standard test method ISO 1133 Condition D at a temperature of 190 ° C and under a load of 2.16 kg , and in which the strict composition distribution amplitude index (CDBI) of polyethylene resin is less than 70%, as analyzed by TREF analysis (fractionation by elution with temperature gradient). In particular, the films according to the invention preferably have an excellent dart force / resistance impact and / or excellent tear resistance both on the machine and optionally transverse directions and / or excellent resistance to slow breaking, at the same time, with much good optical properties, namely fog and / or brightness. In one embodiment, said film has a dart impact force (g / pm) measured according to ISO 7765-1, which is at least equal to the value expressed by the following equation Dart> 1.4 * 2.01 + 22.9 ((7-0.91815) /] + e /(1.004119 where d is the density in g / cm 3 as measured according to the ISO 1183 standard test method at a temperature of 23 ° C. Preferably, the film has an impact force of hair darts 1.3 * less (115 / ττ) * ^ α tanp ^ 0.92736) ^ 0.00453322)] + 0 - 5 * - T J for densities of d between 0.920 and 0.945 g / cm 3 . For example, for resin with a density of 0.930 g / cm 3 , the phyme may have a dart impact resistance of a value of at least 4.5 g / pm measured according to ISO 7765-1, for example For example, a dart impact resistance of at least 4.75 g / pm, preferably at least 5 g / pm, more preferably at least 5.5 g / pm. In one embodiment, said film has an Elmendorf tear resistance in the machine direction (N / mm), measured according to ASTM D 1922, which is greater than or equal to the value expressed by the following equation: TearM> 1.3 * (d- 0.92736) / / (- 0.00453322) where d is the density in g / cm 3 , as measured using the ISO 1183 standard test method at a temperature of 23 ° C, and where the argument of atan is expressed in radians. Preferably, the film has an Elmendorf tear resistance in the machine direction of at least 1.3 * ίιις / Ui r fU-0.92736) / j (115 / t) ^ atan ^ /(-0.00453322)) + 0.5 * for densities between 0.920 and 0.945 g / cm 3 . For example, for a resin that has a density of 0.930 g / cm 3 , the film may have an Elmendorf tear resistance in the machine direction of at least 38 N / mm, preferably at least 40 N / mm, measured from according to ASTM D 1922. In one embodiment, the film has a slow puncture resistance of at least 65 J / mm, measured according to ASTM D5748, more preferably a slow puncture resistance of at least 70 J / mm, more preferably at least 75 J / mm. In one embodiment, the film has a brightness of at least 40% measured according to ASTM D-2457 with an angle of 45, more preferably, a brightness of at least 45%, preferably at least 50%. In one embodiment, the film has a gloss less than 20% measured according to ISO 14782, more preferably a gloss less than 19%, preferably less than 17%, more preferably less than 16%. Examples of articles and products that can desirably be prepared using polyethylene resin compositions can include blown films and fused films. Blown films can include, for example, films used as geoliners, that is, in the soil, linings used to prevent contamination of groundwater in the surrounding soil and by materials found in leaching, for example, the collection of waste and chemical dumps . Other blown film applications include garment bags and / or liners, bread bags, bag making and the like. Polyethylene resin compositions can be used 25/50 in a wide variety of thicknesses and as one or more layers of a multilayer film structure. In other embodiments they can be used as a coating or can, like films, be coated or subjected to fluorination or other treatments to increase their barrier potential for these and other uses. Films are also suitable for use in or as articles designed for packaging, in particular food packaging, construction, insulation, and as laminating films, etc. Any known film blowing line equipment can be used to prepare molten films comprising the resin composition of the present invention, for example, Macchi ® 's COEX FLEX ®. The process parameters that can be used are well known to the person skilled in the art, depending on the desired application of the film. For example: The diameter of the die can vary from 50 to 2000 mm. For example, 50 millimeters would be used for film applications, for example, smaller bags for example for medical purposes, and on the other hand 2,000 millimeters would be used for larger applications, such as agricultural film applications. The blowing ratio (BUR) can be from 1 to 5. The slit die can be 0.8-2.6 mm. The flow rate can be 10 kg / h to 2,000 kg / h. The extrusion screw can have a diameter of 30 mm to 150 mm. Preferably, the screw is a barrier screw. The resin composition can also be used to prepare molten films. Typical film equipment is provided by Dolci, SML etc. Once again, the expert would know how to execute the cast film line to obtain the best possible results. Preferably, the film is 10 pm to 500 pm thick, more preferably 10 to 100 pm, more preferably 10 to 75 pm. The polyethylene resin composition according to the invention can be used to prepare the films, which are monolayer or multilayer. Preferably, the film is monolayer. The monolayer film can be prepared from the polyethylene resin composition according to the invention in combination with other resins, such as LDPE, that is, the film comprises the polyethylene resin composition according to the invention. More preferably, the monolayer film is prepared essentially from the polyethylene resin composition according to the invention, that is, the film essentially consists of the polyethylene resin composition according to the invention. 26/50 In a multilayer film, the polyethylene resin composition according to the invention can be used in one or more layers, either alone or in combination with other resins. Dart impact resistance, Elmendorf tear resistance and slow puncture resistance are mechanical properties that can be important for polyethylene films, depending on your application. The polyethylene resin composition used to prepare films can also exhibit a similar or even improved dart impact force when compared to prior art polyethylenes of comparable density. For example, the F50 dart impact resistance of the film prepared with the resin composition according to the invention can be at least 180g (which is the weight of the hammer required to break the film of 50% of the samples - F50) , preferably at least 190 g, more preferably at least 200 g, even more preferably at least 210 g, more preferably at least 216 g, as measured on a 40 µm thick film. Thus, the dart impact force (expressed in grams per pm of film thickness, g / pm) of the film prepared with the resin composition according to the invention can be at least 1.45 * 2.01 + 1.4 * 22.9 22.9 (rf — 0.91815} /, ,, /0.004119 1 1 fc 'J preferably at least (</•0.91815} / J /0.004119 more preferably, at least 1.5 * The F50 dart impact resistance is measured according to ISO 7765-1, method A (hammer diameter 38.1 mm, drop from height cm) at 23 ° C with 50% humidity. F50 dart impact resistance is measured at 40 pm thick blown film prepared using blown film line equipment that has a collar in configuration with the 45mm extrusion spindle diameter, a length to screw diameter ratio of 30, a diameter of 120 mm and die, a blowing ratio (BUR) of 2.5, a die opening of 1.4 mm, a freezing line height of 320 mm, and the cooling air at a temperature of 20 ° C. Tear resistance Elmendorf was measured in the machine direction (MD) and in the transverse direction (TD). In the direction of the machine, resistance to 27/50 tear of the film prepared with the resin composition according to the invention can be at least 1.3 * Γ (115 / .τ) * ^ α tan ^ J θ ' 2 ' 0 <0 0453322)) + ° · 5 * ' τ ) N / mm (ie average Elmendorf tear strength in N per mm of film thickness), preferably at least 1.35 * (11 5 /, t) * (a lan (<>. 92736 ^ θ J + 0.5 * .r) N / mm, more preferably at least. , Hr / -0.92736) / Ί tar /4-0.00453322)/ 0,5 π J The tear resistance of film Elmendorf prepared with the resin composition according to the invention, in the transverse direction is preferably at least 170 N / mm, preferably 180 N / mm, even more preferably at least 190 N / mm, and more preferably, at least 200 N / mm. Tear resistance can be up to 220 N / mm or 210 N / mm in the transverse direction. Elmendorf tear strength measurements were performed according to the ASTM D 1922 standard, a 40 pm thick blown film prepared using a blown film equipment line that has a collar in configuration with the 45mm extrusion spindle diameter, a length to screw diameter ratio of 30, a die diameter of 120 mm, a blowing ratio (BUR) of 2.5, a die opening of 1.4 mm, a freezing line height of 320 mm, and the cooling air to a temperature of 20 ° C. The resistance to slow puncture of the film prepared with the resin composition according to the invention can be at least 65 J / mm of film thickness, preferably at least 67 J / mm, more preferably at least 70 J / mm, even more preferably at least 72 J / mm, and most preferably at least 75 J / mm. The resistance to slow puncture can be up to 110 J / mm, preferably up to 100 J / mm or 95 J / mm. These measurements were made according to ASTM D5748, that is, with a force of 200 N, a diameter of the puncture rod of 0.75 in, a preload of 0.1 N, a drilling speed of 10 inches / minute, carried out at an ambient temperature of around 23 ° C, on a blown film having a thickness of 40 pm prepared using a blown film line equipment that has a narrowing configuration 28/50 inward with an extrusion screw diameter of 45mm, a length to screw diameter ratio of 30, a die diameter of 120 mm, a blowing ratio (BUR) of 2.5, a die opening 1.4 mm, a freezing line height of 320 mm, and the cooling air to a temperature of 20 ° C. Brightness and fog are significant optical properties for polyethylene films. The polyethylene resin composition can be used to produce films that exhibit less than about 20% fog, preferably less than 19%, more preferably less than 17%, even more preferably less than 16%, more preferably less than 15%. This can be achieved without using any clarity-enhancing agents, i.e., nucleating agents. (In any case, polyethylene nucleating agents do not improve fog much., For example, nucleation can improve a mist from 30% to at least 25%). Thinner films exhibit much less haze, which equates to greater clarity / transparency. However, even films that are thicker have demonstrated better fog values, while still retaining other mechanical properties. % Fog is measured according to ISO 14782, here with a thickness of 40 pm. Gloss performance is also very good for films produced with the inventive polyethylene resin composition, measuring at least 40% for a film thickness of 40 pm. The brightness is preferably at least 45%, more preferably at least 46%. The brightness can be up to 65%, or up to 64%. Brightness here is measured according to ASTM D-2457 at an angle of 45 °. It can be measured with reflectometers, for example, a Byk-Gardner microBright reflectometer. Both brightness and mist are measured in 40 pm thick blown film prepared using a blown film line equipment that has an inward narrowing configuration with an extrusion screw diameter of 45mm, a length to screw diameter ratio of 30, a diameter of 120 mm and die, a blowing ratio (BUR) of 2.5, a die opening of 1.4 mm, a freezing line height of 320 mm, and the cooling air at a temperature of 20 ° C. GEOMEMBRAN APPLICATIONS The present invention also encompasses geomembranes produced by extrusion of flat sheets or by extrusion of molten sheet 29/50 comprising metallocene-catalyzed polyethylene resin according to the first aspect of the invention. In particular, the present invention encompasses a geomembrane comprising a metallocene-catalyzed polyethylene resin having a multimodal molecular weight distribution, comprising from 45% by weight to 75% by weight of a low density fraction, said fraction having a density less than or equal to 918 g / cm 3 , measured according to the ISO 1183 standard test method at a temperature of 23 ° C; wherein the density of the polyethylene resin is 0.920-0.945 g / cm 3 ; where the M w / M n of the polyethylene is 2.8 to 6; where the MI2 melting index of polyethylene resin between 0.1 and 5 g / 10 minutes, measured according to the standard test method ISO 1133 Condition D at a temperature of 190 ° C and under a load of 2.16 kg , and in which the strict composition distribution amplitude index (CDBI) of polyethylene resin is less than 70%, as analyzed by TREF analysis (fractionation by elution with temperature gradient). Accordingly, the present invention provides applications for geomembranes produced by extrusion of flat sheets or by extrusion of sheets blown with a polyethylene resin according to the first aspect of the invention. In one embodiment, the fixed extrusion sheet is preferred. The methods used to prepare geomembranes can be by extrusion of flat sheets or extrusion of molten sheets. In both methods, an extruder can be used. The pellets can be fed into the extruder, for example, by a screw system, which can then be heated, placed under pressure and formed into a hot plastic mass before reaching the die. Since the components are in the hot plastic state, they can be formed into either a flat sheet of a dove tail or a cylindrical sheet which is subsequently cut and folded out to form a flat sheet. In the flat sheet extrusion process, the hot plastic mass is fed into a lofted tail mold and exits through a straight horizontal slit. Depending on the width of the die, one or more extrusion machines may be required to feed the hot plastic mass into the die. High-quality metal lubricants, placed in front of the gap, are used to control the thickness and quality of the leaf surface. These rollers are capable of sustaining pressure and temperature variations without deformation and they are connected to coolants. The rollers are designed to control the thickness of the variation sheet below 3% over the entire width. 30/50 A third bearing can be used to further cool the sheet and to improve the surface finish. The surface finish of the sheet is directly proportional to the quality of the roll surface. The uniformly cooled finished material is then fed along support rollers to be wrapped in a core tube and wound. In the melt extrusion process, the hot plastic is fed into a slowly rotating spiral die to produce a cylindrical sheet. The cooled air is blown into the center of the cylinder to create sufficient pressure to prevent it from collapsing. The plate cylinder is fed vertically: it is then closed because it is flattened on a series of rollers. After the cylinder is folded together, the sheet is cut and opened to form a flat surface and then rolled up. The annular groove through which the cylinder sheet is formed is adjusted to control the thickness of the sheet. Automatic thickness control is available on modern plants. Cooling is carried out by cold air blown into the center of the cylinder and then during the rolling process. Coextrusion allows the combination of different materials for a single multi-layer sheet. The geomembrane may additionally contain customary additives well known to those skilled in the art, such as, for example, carbon black. These additives can be present in amounts generally between 0.01 and 10% by weight based on the weight of the polyethylene. For example, the geomembrane can comprise from 1 to 4% by weight of carbon black, for example 2 to 3% by weight. GRASS WIRE APPLICATIONS The present invention also concerns yarns with the polyethylene resin according to the invention, in particular for cutting the film and monofilaments suitable for tufting on artificial turf or also known as artificial turf. The present invention also encompasses tufts of artificial slit grass or monofilaments comprising metallocene-catalyzed polyethylene resin, according to the first aspect of the invention. In particular, the present invention encompasses a yarn, and preferably an artificial grass comprising a metallocene-catalyzed polyethylene resin having a multimodal molecular weight distribution, comprising from 45% by weight to 75% by weight of a low fraction density, said fraction having a density less than or equal to 918 g / cm 3 , measured according to the ISO 1183 standard test method at a temperature of 23 ° C; where the density 31/50 of the polyethylene resin is 0.920-0.945 g / cm 3 ; where the M w / M n of the polyethylene is 2.8 to 6; where the MI2 melting index of polyethylene resin between 0.1 and 5 g / 10 minutes, measured according to the standard test method ISO 1133 Condition D at a temperature of 190 ° C and under a load of 2.16 kg , and in which the strict composition distribution amplitude index (CDBI) of polyethylene resin is less than 70%, as analyzed by TREF analysis (fractionation by elution with temperature gradient). Polyethylene for slit film and monofilaments for artificial grass can additionally. contain usual additives well known to those skilled in the art, such as antioxidants, stabilizers, processing aids, fillers, flame retardants, colored pigments or the like. These additives can be present in amounts generally between 0.01 and 15% by weight based on the weight of the polyethylene. The yarn (film slit and monofilaments) are suitable for use on artificial lawns or grasses, including synthetic sports surfaces. The film or monofilament slit or the like, according to all aspects of the present invention, can typically be in stretched form. The slit of film or monofilaments or the like, can have a stretch ratio in the range of 1: 3 to 1: 8, preferably 1:03 - 1:06, more preferably 1:03 - 01:04. EXAMPLES The following illustrates the concept of the invention, but in no way limits the scope of the invention. The following polymerizations were carried out in a double circuit reactor, comprising two reactors of RX1 and Rx2 to obtain G to M polyethylene resin compositions according to the invention. The polymerizations were carried out at a temperature of 95 ° C under a pressure of about 40 bars, with a residence time of about 66 min in Rx1 and at a temperature of 83 ° C under a pressure of about 40 bars, with a residence time of about 35 min in Rx2 using an ethylene-bis (tetrahydroindenyl) metallocene catalyst system of zirconium dichloride, with triisobutylaluminum (TIBAL) as the activating agent. The following polymerizations were carried out in a dual circuit reactor, comprising two reactors of RX1 and Rx2 to obtain compositions of polyethylene resin 8G, 8H, according to the invention. The polymerizations were carried out at 32/50 at a temperature of 83 ° C under a pressure of about 40 bars, with a residence time of about 64 min in Rx1 and at a temperature of 83 ° C under a pressure of about 40 bars, with a time of residence of about 34 min in Rx2 using a metallocene catalyst system ethylene-bis (tetrahydroindenyl) of zirconium dichloride, with triisobutylaluminum (TIBAL) as the activating agent. The following polymerizations were carried out in a double circuit reactor, comprising two reactors of RX1 and Rx2 to obtain compositions of polyethylene resin 127, 128, 129, according to the invention. The polymerizations were carried out at a temperature of 90 ° C under a pressure of about 40 bars, with a residence time of about 1.7 hours in Rx1 and at a temperature of 83 ° C under a pressure of about 40 bars , with a residence time of about 0.64 hours in Rx2 using an ethylene-bis (tetrahydroindenyl) metallocene catalyst system of zirconium dichloride, with triisobutylaluminum (TIBAL) as the activating agent. Information on the physical properties of the resin compositions can be found in Table 1a and Table 3. Information on the polymerization conditions in Rx1 and Rx2 can be found in Tables 1b and 1c, respectively. The molecular weight (M n (numerical average molecular weight), M w (average molecular weight by weight) and M z (average molecular weight z)) and molecular weight distributions of d 'were determined by size exclusion chromatography ( SEC) and determined by gel permeation chromatography (GPC). Briefly, a GPCV 2000 - Waters was used: 10 mg of polyethylene sample was dissolved at 160 ° C in 10 ml of trichlorobenzene for 1 hour. Injection volume: about 400 pi, sample preparation and automatic injection temperature: 160 q C. Column temperature: 145 ° C. The detector temperature: 160 ° C. Two Shodex AT-806MS columns (Showa Denko) and one HT6E Styragel (Waters) were used with a flow rate of 1 ml / min. Detector: infrared detector (28003000 centimeter-1). Calibration: narrow polystyrene (PS) standards (commercially available). Calculation of molecular weight Mi of each fraction of eluted polyethylene is based on the Mark-Houwink ratio (Iog10 (M PE ) = 0.965909 - Iog10 (M PS ) 0.28264) (cut at the low molecular weight end to M PE = 1000). The average molecular weights used in establishing weight / molecular properties relationships are the average number (M n ), the average weight (M w ) and the average z (M z ) of molecular weights. These averages are defined by 33/50 following expressions and form M are determined, calculated: yxiT Σ * 1 '·' Σ · / m „= ---- = —- = —-—! i1 VN f MJ, V Λ J There; Then ,, = 4 ----- = J ----- = J _-- v ^ AçAÍ. ^ Af, VAf ; / / X v jv ^ There; v jf ; there; v to ^ there; There- = ------ r = 4 ------ = J ---- v V, Af- VíTAí Vh ; THERE; . I · · f < 1 Here Ni and Wi are the number and weight, respectively, of molecules with molecular weight Mi. The third representation in each case (rightmost) defines how to obtain these averages of SEC chromatograms, hi is the height (from the baseline) of the SEC curve in the elution fraction and Mi is the molecular weight of the species of elution in this increment. The MI2 melt index and high load HLMI melt index are measured by the ISO 1133 Condition D standard test method, respectively, under a load of 2.16 kg and 21.6 kg and at a temperature of 190 ° C. polydispersity index (PI) was determined at a temperature of 190 ° C, using a parallel plate rheometer model ARES-G2 sold by TA instrument (USA), operating at an oscillation frequency that increases from 0.1 rad / sec to about 300 rad / sec. From the passage module, PI can be derived by means of the equation: PI = 10 6 / Gc where Gc is the crossing module, which is defined as the value (expressed in Pa) where G '= G, where G is the storage module and G is the loss module. The CDBI (the strict composition distribution amplitude index) is a measure of the distribution amplitude of the copolymer composition, with respect to the level of comonomer incorporated in the polymer, this reduction in the crystallinity of domains made from such polymeric chains by means of a short side chain branching in relation to the crystalline homopolymer. This is described, for example, in WO 93/03093. CDBI is defined as the percentage, by weight, or mass fraction of copolymer molecules that have a comonomer content of ± 25% of the average total molar comonomer content, that is, the percentage of 34/50 comonomer molecules with a comonomer content is within 50% of the average comonomer content. CDBI was determined from the accumulated SCB distribution obtained by TREF (increasing temperature eluting fraction) analysis (tempering or slow cooling conditions). TREF analysis was performed using a Polymer Char TREE instrument (Valencia, Spain). TREF conditions were as follows. Hardening-ATREF (analytical TREF): a solution of 1 mg / ml of polyethylene resin in 1-2-4 trichlorobenzene (TCB) was obtained by dissolving at 160 ° C for one hour. The solution was injected into the ATREF column at about 30 ° C with a flow rate of 0.5 ml / min. The precipitated polyethylene column was then eluted at a heating rate of 2 ° C / min to 130 ° C. The flow rate was 0.5ml / min during the elution step. Classic ATREF: a 0.05% (0.5 mg / ml) solution of polyethylene was prepared as described for the 160 ° C quenching TREF and was injected into the ATREF column and allowed to cool slowly (to 6 ° C / h) from 100 to 30 ° C. The flow rate during heating from 30 ° C to 120 ° C was 0.4 ml / min and the heating rate was 1 ° C / min. PTREF (preparative TREF): The sample (about 6 g) was dissolved in xylene at 130 ° C at a concentration of 1 g / 100 ml. The hot solution (stabilized with 1000 ppm Irganox 1010) was loaded into the glass tube of the PTREF device at a temperature of 130 ° C. The PTREF column was then cooled at a rate of 2.4 ° C / h to 30 ° C (42 h). After precipitation of the polyethylene on the column filling, the low density fraction was recovered by heating to a temperature that is guided by classic ATREF in TCB: the separation temperature is approximately equal to the ATREF temperature corresponding to a level of SCB that will give a density of about 0.92 g / cm 3 (SCB 10/1000 C) of less than 10 ° C (as PTREF is done in non-TCB xylene). This corresponds to this PTREF device at 77 ° C. After 30 minutes at the chosen temperature, the first fraction was then obtained by connecting the column to a recovery tank, through which the solvent was pumped at 10 mUmin. The higher density fraction was then obtained by elution at 100 ° C, under conditions similar to those used for the first fraction. Both eluted fractions were precipitated in methanol, filtered through PTFE filters and dried. Column dimensions (ATREF): 150x3.9 mm (WxD), 1.8 ml internal volume, DRI detector (differential refractive index), geometric column resolution: heating rate (° C / min) * The volume load (ml) / flow rate (ml / min): 35/50 3.6 ° C / column. The loading volume was about 0.8 x column volume (80% packaging material). For ATREF temper, the column's geometric resolution was 5.76 ° C / column. Calibration for SCB (elution temperature SCB) was established for each condition using several monomodal MPE resins (compositional distribution index width, CDBI,> 94%) by classic ATREF) density, 9230.955 g / cm 3 synthesized with the same comonomer and system catalyst such as the polyethylene resin according to this invention. Figure 1 shows Chemical Composition Distribution (CCD) curves obtained for resin 129 with two ATREF cooling conditions (temper, 6 ° C / h). For comparison, the comparative example of a monomodal polyethylene resin, catalyzed by metallocene obtained with the same catalyst system was tested. The bimodal character of resin 129 was apparent as a TREF tempered shoulder and as two well-separated peaks for slow-cooling TREF (classical TREF). Figure 2 shows ATREF profiles for resin 129 and resin 8H, and compared to two monomodal mPE (density 0.923 g / cm 3 and 0.934 g / cm 3 ) and bimodal PE GX4081 from Basell. The ATREF profiles were bimodal for resin 129 and 8H. Bimodal PE resin GX4081 exhibits a skewed CCD curve in the high SCB direction with no clear sign of bimodality under ATREF attenuation conditions. For the two monomodal MPE resins, a large monomodal peak was observed and the SCB weight fraction calculated from ATREF monomodal MPE tempering resins (9.2 / 1000 C and C 4.4 / 1000 to 0.923 and 0.934 g / cm 3 , respectively) agreed with the NMR values. After converting the temperature axis to the SCB axis (Figure 3), the amount of HDPE crystals (seen as SCB = 0) was very high for GX4081 and no peak was observed for the remaining resins. This means that the amount of co-crystallized was low and very large. The resin 129 exhibited a clear bimodal composition (shoulder) and the measurement of eluted crystals was narrower than for GX4081. The 8H resin exhibited a clear bimodal composition distribution. Without being limited by theory, it is believed that, in order to have good mechanical properties, the peaks corresponding to LLDPE and HDPE must be well separated (this will give a low CDBI) and for good optical properties, co-crystals must be formed within a narrow range of crystallization temperature (which corresponds to the elution temperature or apparent SCB). 36/50 In Figure 4, the cumulative distribution (same resins as in Figure 3) are needed to calculate the CDBI, as taught in W093 / 03093 (p. 18-19 and Figure 17) are shown. The CDBI values computed from the cumulative distribution are shown in Table A. TABLE A Resin CDBI (%) TREF temper 129 42 GX4081 20 single-mode mPE density 0.934 g / cm 3 75 8H 66 single-mode mPE density 0.923 g / cm 3 93 From Figure 1, it is evident that the low density fraction of resin 129 is narrow (CDBI> 90%). In effect, from the low density fraction recovered (52%), an ATREF quench was conducted and from its cumulative distribution curve, a CDBI of 89.6% was derived. ATREF in the classic mode in which the low density fraction gave a CDBI of 98% (Figure 5, Table 2). g rheo is determined according to the disclosure, in WO 2008/113680: M (SEC) e. (PE) = ---------------------- Mjj ^ .MWD.SCB) Where M w (SEC) is the average molecular weight obtained from size exclusion chromatography, expressed in kDa, as described above, and where M w (ηΟ, MWD, SCB) is determined according to the following: M K. (Q 0 , MWD, SCB) = exp (.1.7789 + 0.199769LnM H + 0.209026 (Ln η () ) + 0.955 (In p) - 0.007561 (LnM 7 } {Ln / (! ) + 0.02355 ( ln M ; ) 2 ) The value of Mw (ηΟ, MWD, SCB) was determined by dynamic rheological analysis (RDA) and is equal to Mw (SEC) for linear PE (PE without LCB). Zero shear viscosity is proportional to Mw (SEC) to end power of 3.4th (in our case, to about 3.6 to power). Corrections due to molecular weight distribution and short chain branching (SCB) are used to describe zero shear viscosity as a function of molecular weight (SEC). Therefore, this is why 37/50 that, beside zero shear viscosity, Mn and Mz, as well as ρ (density, d) appear in the relative expression Mw (ηθ, MWD, SCB) determined by rheology to zero shear viscosity. For linear PE, g rheo is equal to 1.0 +/- 0.05. If, at a given value Mw (SEC), zero-cut viscosity increases above that of a linear PE, then g rheo will be less than 1. P density is measured in g / cm3 and measured according to ISO 1183, at a temperature of 23 ° C. Zero shear viscosity ηθ in Pa.s is obtained from a frequency sweep experiment combined with a creep test, in order to extend the frequency range of displacement values of 10-4 s-1 or less, and having the usual assumption of equivalence of angular frequency (rad / s) and shear rate. Zero shear viscosity ηθ is estimated by fitting with Carreau-Yasuda flow curve (η-W), at a temperature of 190 ° C, obtained by oscillatory shear rheology in ARESG2 equipment (manufactured by TA Instruments) in the domain of linear viscoelasticity . Circular frequency (W in rad / s) ranges from 0.05-0.1 rad / s to 250-500 rad / s, typically 0.1-250 rad / s, and the shear strain is typically 10%. In practice, the creep experiment is carried out at a temperature of 190 ° C under a nitrogen atmosphere, with a stress level such that after 1200 of the total deformation it is less than 20%. The device used is an AR-G2 manufactured by TA Instruments. The polyethylene resin compositions were transformed into 40 mM thick blown films using blown film line equipment from Macchi R. having an inward narrowing configuration with a screw extrusion diameter of 45 mm, the length of a screw diameter ratio of 30, a die diameter of 120 mm, and a blowing ratio (BUR) of 2.5, a die opening of 1.4 mm. a freezing line height of 320 mm, and the cooling air at a temperature of 20 ° C. The mechanical and optical properties can be found in Tables 3 and Table 4, compared to prior art commercial resins: Lupolen GX 4081 (from Basell), Borstar FB 2310 (from Borealis), 1018CA (from Exxon), HF513 monomodal Cr-catalyzed polyethylene (Total Inputs), Marlex D350 (Chevron Phillipps) and a mPE monomodal (Total Inputs), also prepared with an ethylene-bis (tetrahydroindenyl) -zirconium containing metallocene catalyst system. and resin 780B and 780D (Total Inputs), which are medium density bimodal polyethylene prepared with ethylenebis (tetrahydroindenyl) zirconium in a double circuit reactor. The results show that the compositions 38/50 of polyethylene resin according to the invention has a better balance of optical and mechanical properties. Lupolen GX 4081 (from Basell) and Borstar FB 2310 (from Borealis), for example, have good mechanical properties, but very low brightness and high fog, while single-mode mPE has very high brightness and low fog, but mechanical properties that are not so suitable for certain film applications. In addition, for Lupolen GX 4081, processing is worse (higher extrusion pressure, less stability). The resins of the invention however retain very good mechanical properties, such as tear strength, puncture resistance, slow and dart impact resistance, at the same time, with very good optical properties. This was made possible (without being theoretically limited) by increasing the proportion of low density, high molecular weight fraction in the resin composition prepared using catalytic systems based on bisindenyl or bistetrahydroindenyl metallocene. It should be noted that particularly surprisingly, the slow bore for the polyethylene resin composition according to the invention was greater than for the monomodal equivalent. using the same catalyst, although the opposite was actually expected. It has also been observed that the polyethylene resin compositions according to the invention are also easily processable due to their high melt strength. Also less neck-in was observed during the blowing of the films. GEOMEMBRANES Stress breaking strength was assessed after the complete notched Creep test (FNCT), measured according to ISO 16770. The test uses a rod-shaped sample with the following mm dimension 90x6x6 with a notch depth of 1 mm, to determine the resistance of the material to brittle fractures caused by long term, low level of tensile stress. The test according to the ISO 16770 standard test method requires that the samples be placed in a surfactant solution, selected here as a 2% Maranyl solution, at a temperature of 50 ° C, for an extended period of time, and be subjected to a tensile tension equal to 9 MPa. The results for the mean failure time are shown in Table 5. The results were compared with two comparative resin (a) a monomodal metallocene-catalyzed polyethylene (mPE1) having an MI2 of 0.2 g / 10 min and a density of 0.933 g / cm3, and (b) a monomodal metallocene-catalyzed polyethylene (mPE2) Having an MI2 of 1.0 g / 10 min and a density of 39/50 0.934 g / cm3. mPE1 is normally used in geomembrane applications with acceptable properties. Resistance to crack stress for mPE1 and mPE2 was assessed following the single point notched constant tension load (SPNCTL). The test used a bell-shaped mute notched specimen to determine the material's resistance to brittle fractures caused by long-term, low-level stress stress. The test according to the standard test method ASTM D 5397 requires that the samples be placed in a surfactant solution, selected here as an Ipegal 10% solution, at a temperature of 50 ° C, for an extended period of time, and be subjected to a tensile stress equal to 15% of the yield strength of the material. In the field of geo-membrane applications, failure may not occur before at least 400 hours of exposure. mPE1 failed the test with an SPNCTL of less than 400 hours, while mPE2 showed an SPNCTL of over 400 hours. In view of these FNCT results for mPE1 and mPE2, by extrapolation, the current resins must have good SPNCTL behavior, thus showing their suitability for geomembrane application. GRASS WIRE. Resins I and M were tested on a Compact Oerlikon Barmag line (Oerlikon Barmag, Germany), and compared to a monomodal metallocene A resin. The comparative resin characteristic A is shown in Table 6. The wires were prepared and tested using the following conditions: - Revenue: 6% by weight of one MB BASF color / UV (Sicolen 90010365) + 1% by weight of Viba PPA (733E); - Titre: 2000 dtex monofilaments - 4 * 12 filaments emerging from a spinneret. - The extrusion was carried out at T °: 190/220 ° C and at 230 ° C in the die section. - T ° water cooling bath: 35 ° C. - 3 stretching in air furnaces - Melt fracture was assessed by touch, when the wire was completely smooth to the touch, a score was NOT assigned. When the thread was completely rough the score was YES. Intermediate roughness received YES / NO. 40/50 The results are shown in Table 7. Compared to resin A, the present resins have been found to improve maximum speed without melting fracture and reasonable pressures. Compared to resin A, the resins present are capable of allowing a decrease in the die pressure of about 5% by 20%, and a delay in the appearance of the melting fracture on the threads. The present resins can be executed at a higher speed, such as a + 50% increase in speed compared to resin A (100 m / min vs 67 m / min). 41/50 TABLE 1a | C6 (weight%) 4.7 CO 3.9 CO 5.9 6.6 4.4 CMIn (Mw)) z ) > Φ19 82.5 83.7 81.8 87.2 i1 06 85.7 109.5 109.6I s 94.1 83.4 CXI LD CO ID P·-. CO CM COCD p ~~ ^ yCO <= Q I CM THE «- cm ’ CD CD co ’ CDCO T5 LO CM CM CM CM CMCM CM CM CM CM Ç The' Φ CM 0 Φ _ CM ooCO s Q -Μ CO THE' CO THE' CO CM CD THE w dCO co CO CO CO CO CM CM CM CO CO The σ> CD CD CD CD CD CD CD 0) CD CD Ό> 0) ό THE THE THE THE The d d d The THE R * co CXI O COCD ps_. CO Ό C SÈ S ’ 60 THE80 9Ό 8Ό CM d co d 0.6 XT 0.6 CM p2 CXIXd (X co s + co LT) COThe' crρ ^ _ - CD CO CO CO CMco Thes T ~ 3ρ · ^ IDco CM CD LD CD co co COCM CO»Y ’T - <y CO CO cm ’ co cm ’ S'. X (Ο The CO co CD THE CD . The co 00 The Φ *** '.CD CO p ~ _ COpH ^ p ^ co The LDΦ Q CXJ CD The" CO co ’ oo ’ LD cm ’ CD co " II w- 1 T CM CM CM CM LD CDco CM Τ— 7— i— ’- Ί-- 1--- ι— T-- 1--- 1- T " ω ^ -. ρ »» co co The CM 00 co CD P*-. Ί ç ΦQ COCO co CD 9.5 CO ID d 6’6 2.5 4.7THEΞ 2 • <y THE'xj · THE' LO CD ^ y LD ^ p φΦ Ό II to ΦCO T2 «Ε CO p ^ CO LD p ^ _ CM CO LD CM CO ^ y <ΰ _Q S2r ι 'r— T ““ T T ç shut upder •S σ> ό 0.9 CDTHE 0.9 CD d 0.9 6'0 (DThe ~ 0.9 60 6Ό Μ— It's the 6 XI ο co CO THE' CM co CM CMLD CO LDCO ο The THE THE The THE THE THE THE The THE ç "THE The 'S' ό THE THE THE d d d d d d dat the ω Ε AND Φ S CM CM CM CM co CM ’’ T co CM CM CM ω to CLTHE' THE' ^ y cosy ^ y 'y · ^ y ^ y φ ω Φ ίΛ .— px_ &) CO CM CM00 LD ID IDΦ φ CO co 00 CM 1 CO co CO C3Φ3 Q θ ' • ^ y CO CD CD ID d , - CD d d _Q to ü.z> co CM CM CM CM THE' ^ y • M-ΦLO ID CD CD ^ y CDP"_ p ^ _ P"_ d 73 φ CO THE)CD THE LD THE 00 ^ y ^ y ^ y The THE ç Q co " co " I --- ·, - CM Q> CO CD CD CD d The Q. Ξξ T - T ~ 1 - Φ AND Φ Ό · Ζ ( 1 <5 'Φ TheΦ 0-QAND ιφ Ε LO co THE CMCO THE CD LD LD LD to CM LO LD co CD CD CD co CM LD LD ID ç at ® XΦCD CD CD CD 05 CD CD CD CD CD CD Φu crQ S' THE d THE d d d d d d d d ΌTHE Φ ç ιφ ο THE ID The THE THE_ The_2 xCMTHECO 2.0 CO O 8.0 THE THE 7.4 00od 6.0 6.0 0'9 The73 ro ll cr CM LO T— CD CD T - CM CM CM CM co dog ο «'φ Icul to Φcn <= ίζΓ CO coThe Ω ω Φ Φ> The t QC, Ε CD CO CM CXITheTHE Φ φ Ό ΌCD _ —3l000 ΞΕ oo CM7— CMT— CM1- 2 42/50 TABLE 1b Rx1 Reaction conditions H2 / C2OG0.001 0.001 L00O Τ-Ο ο ό what is T- Ο 1- o o o o o o o o q ο ο ο ο oÓ Ô o o o o ’ C6 / C2 OG60Ό 0.09 Τ-Ο 00 ο Ô <o o d 00 LO 7- T— the CDq CO CD Ή- 7— oÔ Ô O Ô d o hydrogen(H2) Off-gas VOL% 0.01 0.01 0.01 ο ο TheThe Ί- o o o o o ο ο O o o o o o o o d o ’o’ o ’ Hexene (C6) Off-gas sPThe ω Φ 0.54 0.54 0.63 οLO ο co co Ô LO CO CO O h-LO CM Xf CO CM CM ^d <- d d d d Ethylene (C2)Off-gas 1 Weight% 5.87 5.93 5.74 CO ο có CMd co co LO o io oCM in CD The CDd d d cm ’d d isobutane 0) 60 60 60 ο co the co o o oo o oΟ Ο O 1- ΤΟ LO LO CM CM CM Hydrogen feed Normal liter / h 25.5 31.2 37.0 οd co TheCD co o o o θ Qd d d m οLO Ο LO m LO LOTj · 7— cm 'st Hexene feed kg / h 0.28 0.28 Οό LO CM ο d CD Ο OCM CM qqqO 00 ”3- CO CO CM Power supplyethylene kg / h 22.0 22.5 22.5 LOCM CM LOCMCM LO CD cd θ’D d Ο Ο OCMt-7-7 ^ 7—7—CM CM CM CO CO CO Tibal ppm 313 302 313 m CD CM CM O CO CM CO with O 7- 7- with CD with co-co - 'T Composition of the resin of the inventionCD z —I / n _ Γ- · CD 00 - 0 T CM CM CM CO 00 7— 7— 7— 43/50 TABLE 1c <n C Oτ5 c o oc othe fú Φ CCCM X02 C6 / C21.32 1.50 1.59 1.71 1.30 1.29 96Ό 1.06 S6’0 0.95 0.93 hydrogenOff-gas VOL% THE THE THE THETHE THE THE THE THE THE Hexene Off-gas Weight % 6.33 7.17 CO 7.40 6.50 5.53 3.30 3.95 4.879 4.77 4,747 Off-gas ethylene Weight % CT) co 4.26 4.33 5.00 4.30 3.48 3.72 5.12 4.99 5.12 isobutane 15) to 45 THE 45 LO to IO IO 3430 3545 3430 Hydrogen feed Normal liter / hCO m LO COCM CM 1195 845 1200 Hexene feed6.55 6.55 6.70 7.20 7.20 7.00 3.70 3.70 559 562 Io Ethylene feed JZ CM CM CM CM 32 CM 29 I 03 CM 4299 | CO O CM xt 4299 Tibal E CL CL 208 194 204 194 208 208 208 194 CM 20 CM Composition of the resin of the invention0 l 2 0 CO 8H CM 129 128 44/50 TABLE 2 CDBI determination H 29 DBI pelet6 2 DBI fraction Rx2M 8 CDBI pelets determined by ATREF temper CDBI fraction Rx2 determined by classical ATREF (cooling rate of 6 ° C / hour), of the fraction obtained by Rx2 PTREF 45/50 2 19218 00LO00 225314 LO 2.6 0.933 0.8 89’0 12.04 5.50.04 1.95 THE CO σ> LO co CXJ LO o σ> 00 o00 CO σ> CD The CD CXI CXJCO00 TheThe 89 '-1 CXJ 00 orCXJ The B B 03CXJ CDB 7-- LO The 7— CO o CO COCONUTS0) 00 CD CD CXI 00 bCXJ The dog CXJ 00 CXJcxi B B B Cxj LOB 7-- 00 CXJLO o CD CXJ CXJ σ>0) -χΓ CO 03 7— CO with LO o The THE"J ç 00 7—cxj THE t— B Ί ---CXJ LOThe 7 “ CD CD σ> lo CXJ CO 03cxJ o CO0003CD CXJCXJ.0303 The δ__ CXI 00 CXJ 00 cxj THE The B 037 “ LOB T " CDThe co CO00 7--CXJ CXJ coCXI 03 03 CD Γ—δ * ζΓThe CDο CXJ coCO Cxj THE THE B COCXJ LOThe 7--X TheV οΦ cg 0000LO σ>co CD LO00 r ^. 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CO ω .Ε φ Ό Q_ Ex The ex rrt ω Ό CLΦ Q -J 'CD Ό -Φ Q αζ Ό Φ 'φ 0 'Φ CD Φ CD Φ σ>S 2 LU 2 2 2 Η co 2 z 2 0 5 5 2 ® 2 ® 47/50 Table 4 - Resin composition and film properties 00 CXJ T - 0.955 42 16.47 40.35 26 0.914 44.07 114.58 2.84 23.4 COCONUTS T—CD^ = · 3.6 129 0.955 CXJ 16.47 40.35 26 0.913 51.16 133.03 3.30 24.7 σ> 224 3.8 c j1- 0.955 CXJ 16.47 40.35 26 0.912 44.73 116.30 2.88 σ>CO CXJ 84.4 σ> CO T - 3.5 8H 0.929 CO 16.81 001- 23.8 0.915 62.58 162.71 3.95 28.4 109.6 280 CD00 000 0.930 ΙΌr— 18.06 44.240.917 59.92 155.79 3.52 29.6 109.5 272 poop 780D 0.944 43 17.20 42.14 23.2 0.927 52.82 137.33 la.36 CXJ 96.4 239 3.5 780B 0.948 00 21.20 51.94 σ> 0.924 48.16 125.20 • 2.41 30.8 93.7 σ>1-CXJ 3.0g / cm3 xP o '·· * OJTHE 03Q g / 10min g / cm3 kDa QMn (kDa) | ra QS s Mz (kDa) D (Mw / Mn) High density fraction density(HDF) HDF weight Mn HDF Mw HDF MI2 HDF Low density fraction density (LDF) LDF Mn LDF Mw LDF Mw / HDF Mw GPC pelet 48/50 2.3 0.931 0.7 IAIN 0.67 8.27 DART 5.90 54.10 194.00 c iCXI cxi 0.930 0.5 IAJN 0.57 9.69 7.30 54.40 o LO o o ex 0.930I THE IAIN 0.62 8.1 6.30 63.70 the CDCO cn t 2.6 0.921 0.3 17 0.48 96'6 the ex Theo 'LO o co to 'coΊ-- 2.5 0.922 0.3 Ί-- 0.40 10.01 Ther—T " the coconut The 2.5 0.934 0.5 20 0.33 10.87 2.90 ooc T T - TheTheΊ-- 2.3 0.934 d σ>Ί— 0.30 7.84 3.45 Themrex the oCD ex1- D '(Mz / Mw) g / cm3 ! g / 1 Orrin g / 10min106 / Gc (Pa-1) ANDThe.cn ! N / mm N / mm Dart / thickness Elmendorf MD average / thickness Elmendorf TD average / thicknessdensity MI2 HLMI grheo CL 49/50 TABLE 5 129 0.932 0.5 > 433 single-mode mPE2ref KO 0.934 THE COt— single-mode mPE1: ref OK 0.933 0.2 COIt's theΌ MI2 (g / 10min) Failure time (h) Q Q O CL Oσ>sc j Φ 0Ό ω CÕ ω φ Ε 00 φ Φ Ο σ> D CL 0) ο toΦΦCXCXJ ο <£>0) THE CCQC Ο ' 1 ' 51.8 OJX CCΦ 0Φ 0 ω LO C ο Ε 00 Φ φ Ο CD 0 0 0) THE ΦΌρ‘Φ πΕ COCO φ * ρ σ> Ό 0C σι ο C J X (XCM ÇΕ ο Ύ “ oõ 2 σ> ο _ο CÜ οX QCCXJ 10 min CDσι Ο φ C co φ £ Ε1203Α 50/50 TABLE 7 Fusion fracture IAIIS YEA YEANOT NOT YES NO YEA NOT NOT YES NOPressure measured in the die (bar) 128 145 166 1 106 co CO 145 102 CO T - T - 129 NM Max speed line (m / min) CD 80 100 120 <S 80 100 120 <O 80 100 120 Experiment reference 1" > > > > V7 > > THET—Resin 1203A 1203A 1203A 1203A 12031 12031 12031 12031 1203M 1203M 1203M 1203M 1/5
权利要求:
Claims (18) [1] 1. Metallocene-catalyzed polyethylene resin characterized by having a multimodal molecular weight distribution, comprising from 45% by weight to 75% by weight of a low density fraction, said fraction has a density less than or equal to 918 g / cm 3 , measured according to the ISO 1183 standard test method at a temperature of 23 ° C; wherein the density of the polyethylene resin is 0.9200.945 g / cm 3 ; where the M w / M n of the polyethylene is 2.8 to 6; where the melt index MI2 of polyethylene resin from 0.1 to 5 g / 10 minutes, measured according to the standard test method ISO 1133 Condition D at a temperature of 190 ° C and under a load of 2.16 kg; where the strict composition distribution amplitude index (CDBI) of polyethylene resin is less than 70%, as analyzed by TREF analysis (fractionation by elution with temperature gradient; and in which the polyethylene resin has a g r heo less than 0.80, which g r heo can be determined according to: MJSEC) * '* e M w ^ 0 , MWD, SCB) where Mw (SEC) is the weighted average molecular weight obtained from size exclusion chromatography expressed in kDa, and where Mw (ηθ, MWD, SCB ) is determined according to the following: M h . (/ 7 0 , MWD, SCB) exp (1.7789 + 0.199769LnM „+ 0.209026 (Lnη 0 ) + 0.955 (] np) - 0.W15 (A (LnM z ) (Lnf ^) + 0.02355 ( ln M _) 2 ) where the density p is measured in g / cm3 and measured according to ISO 1183 at a temperature of 23 ° C, and where the zero shear viscosity ηθ in Pa.s is obtained from a frequency sweep experiment combined with a fluency experiment to extend the frequency range to values less than 10-4 s-1 or less, and Petition 870190133120, of 12/13/2019, p. 19/23 [2] 2/5 assuming the usual hypothesis of equivalence of angular frequency (rad / s) and shear rate, and in which the zero shear viscosity ηΟ is estimated by adjusting the curved Carreau-Yasuda flow (η-W) to a temperature of 190 ° C, obtained by oscillatory shear rheology in ARES-G2 equipment in the domain of linear viscoelasticity and in which the circular frequency (W in rad / s) varies from 0.05-0.1 rad / s to 250-500 rad / s, and the shear stress is typically 10%, and where the creep experiment is performed at a temperature of 190 ° C under nitrogen atmosphere with a stress level such that, after 1200s, the total stress is less to 20%. 2. Metallocene-catalyzed polyethylene resin according to claim 1, characterized in that the M w of the low density polyethylene fraction is 80-140 kDa. [3] 3. Metallocene-catalyzed polyethylene resin according to claim 1 or 2, characterized in that the strict composition distribution amplitude index (CDBI) of the polyethylene resin is at least 30%, as analyzed by TREF analysis (Fractionation) elution with temperature gradient). [4] 4. Metallocene-catalyzed polyethylene resin according to any one of claims 1 to 3, characterized by the fact that the CDBI of the low density polyethylene fraction, as analyzed by TREF using a cooling rate of 6 ° C / hour is over 80%. [5] Metallocene-catalyzed polyethylene resin according to any one of claims 1 to 4, characterized in that the polyethylene resin comprises a fraction having a higher density than the low density fraction, wherein the M w ratio of the low density / M w of the highest density fraction is less than 6 and greater than 2.5. [6] 6. Metallocene-catalyzed polyethylene resin according to any one of claims 1 to 5, characterized in that the polyethylene resin has a polydispersity index (PI) of at least 6.5, wherein the Petition 870190133120, of 12/13/2019, p. 20/23 3/5 referred to a polydispersity index is determined at a temperature of 190 ° C using parallel plate rheometer model ARES-G2, and operating at an oscillation frequency that increases from 0.1 rad / sec to 300 rad / sec, and where PI can be derived from the crossing module using the equation: PI = 10 6 / Gc where Gc is the crossing module which is defined as the value, expressed in Pa, where G '= G, in that G is the storage module, and where G is the loss module. [7] 7. Metallocene-catalyzed polyethylene resin according to any one of claims 1 to 6, characterized in that the polyethylene resin has a g r heo of less than 0.75, where g r heo can be determined according to: grheo ( PE ) = M W (SEC) M w (y 0 , MWD, SCB) where M w (SEC) is the average molecular weight obtained from size exclusion chromatography, expressed in kDa, and where M w (no, MWD, SCB) is determined according to the following: M Jj] 0 , MWD, SCB) = exp (L7789 + 0.199769LnM n + 0.209026 (L «η ϋ ) + 0.955 (ln p) - 0.007561 (LnM z ) (Lnp 0 ) + 0.02355 (lnAÇ) 2 ) where density p is measured in g / cm 3 and measured according to ISO 1183, at a temperature of 23 ° C, and where the zero shear viscosity nO in Pa.s is obtained from a sweeping experiment frequency combined with a creep test, to extend the frequency range to values less than 10-4 s-1 or less, and having the usual assumption of equivalence of angular frequency (rad / s) and cut-off rate, and in that the zero shear viscosity nO is estimated by fitting with a Carreau-Yasuda (nW) flow curve, at a temperature of 190 ° C, obtained by oscillatory shear rheology on ARES-G2 equipment in the linear viscoelasticity domain, and in that the circular frequency (W in rad / s) ranges from 0.05-0.1 rad / s to 250-500 rad / s, and the Petition 870190133120, of 12/13/2019, p. 21/23 4/5 shear strain is typically 10%, and in which the creep experiment is carried out at a temperature of 190 ° C under nitrogen atmosphere, with a stress level such that after 1200 of the total strain is less than 20%. [8] Metallocene-catalyzed polyethylene resin according to any one of claims 1 to 7, characterized in that the polyethylene resin has a fat content of more than 0.35. [9] 9. Film characterized by comprising the metallocene-catalyzed polyethylene resin as defined in any one of claims 1 to 8. [10] 10. Film according to claim 9, characterized in that said film has a resistance to the impact of the dart (g / pm), measured according to the ISO 7765-1 standard, which is at least equal to the value expressed by the following equation: Dart> 1.4 * where d is the density in g / cm 3 as measured using the ISO 1183 standard test method at a temperature of 23 ° C. [11] 11. Film according to claim 9 or 10, characterized in that said film has an Elmendorf tear resistance in the machine direction (N / mm), measured according to ASTM D 1922, which is greater than or equal to the value expressed by following equation: 0.00453322) J + 0.5 * ^ where d is the density in g / cm 3 , measured according to the ISO 1183 standard test method at a temperature of 23 ° C, and where the atan argument is expressed in radian. [12] Film according to any one of claims 9 to 11, characterized in that said film has a resistance to Petition 870190133120, of 12/13/2019, p. 22/23 5/5 slow drilling of at least 65 J / mm, measured according to ASTM D5748. [13] 13. Film according to any one of claims 9 to 12, characterized in that said film has a brightness of at least 40% measured according to ASTM D-2457 at an angle of 45 °. [14] 14. Film according to any of claims 9 to 13, characterized in that said film has a turbidity of less than 20% measured in accordance with ISO 14782. [15] 15. Process for the preparation of a metallocene-catalyzed polyethylene resin as defined in any one of claims 1 to 8, characterized in that said polyethylene resin is prepared in at least two reactors connected in series, in the presence of a catalyst system containing metallocene. [16] 16. Process according to claim 15, characterized in that the metallocene-containing catalyst system comprises a metallocene selected from a bridged bisindenyl metallocene or a tetrahydrogenated bis-indenyl bridged metallocene or a mixture of both. [17] 17. Geo-membrane produced by extrusion of flat sheet or extrusion of molten sheet, characterized in that it comprises metallocene-catalyzed polyethylene resin as defined in any one of claims 1 to 8. [18] 18. Tufts of slit or monofilament synthetic grass, characterized in that it comprises metallocene-catalyzed polyethylene resin as defined in any one of claims 1 to 8.
类似技术:
公开号 | 公开日 | 专利标题 BR112014000435B1|2020-03-31|POLYETHYLENE CATALYED BY METALOCENE EP1613797B1|2013-03-06|Monofilaments or stretched tapes from metallocene-produced polyethylene BR112012022194B1|2020-04-14|polymer composition based on ethylene, manufactured article, thermoplastic formulation and polymerization process WO2008089978A1|2008-07-31|Multimodal medium density polyethylene polymer composition EP2619357B1|2019-08-28|Artificial grass KR20090087880A|2009-08-18|Resin composition for production of high tenacity slit film, monofilaments and fibers WO2008113566A2|2008-09-25|Fibres, tapes or filaments comprising a polyethylene composition EP3635040B1|2020-10-14|Polyethylene fabric, and backing and artificial turf made therefrom JP6006887B2|2016-10-12|Random propylene copolymer for bottles with good optical properties JP5987120B2|2016-09-07|Random propylene copolymer for bottles with good optical properties and low hexane content ES2744081T3|2020-02-21|Polyethylene composition for artificial grass thread JP2004238774A|2004-08-26|Flexible yarn and artificial turf made thereof JP4792741B2|2011-10-12|Easy tear film KR20210023003A|2021-03-04|Polyethylene Resin Composition for Artificial turf fiber, and Artificial turf fiber using the same
同族专利:
公开号 | 公开日 PT2729525T|2020-01-16| HUE046972T2|2020-04-28| US10053522B2|2018-08-21| WO2013007619A1|2013-01-17| TWI460221B|2014-11-11| DK2729525T3|2020-01-02| BR112014000435A2|2017-02-14| CN103781838A|2014-05-07| EP2729525A1|2014-05-14| CN103781838B|2016-04-06| EP2729525B1|2019-10-09| US20140127427A1|2014-05-08| TW201311799A|2013-03-16| PL2729525T3|2020-04-30| CA2839965C|2020-02-25| EA027509B1|2017-08-31| WO2013007619A9|2013-03-07| CA2839965A1|2013-01-17| EA201490227A1|2014-04-30| ES2764413T3|2020-06-03|
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法律状态:
2018-04-03| B06F| Objections, documents and/or translations needed after an examination request according art. 34 industrial property law| 2019-09-17| B06U| Preliminary requirement: requests with searches performed by other patent offices: suspension of the patent application procedure| 2020-01-28| B09A| Decision: intention to grant| 2020-03-31| B16A| Patent or certificate of addition of invention granted|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 06/07/2012, OBSERVADAS AS CONDICOES LEGAIS. |
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申请号 | 申请日 | 专利标题 EP11173375.4|2011-07-08| EP11173375|2011-07-08| EP11173376.2|2011-07-08| EP11173376|2011-07-08| EP11184554.1|2011-10-10| EP11184553|2011-10-10| EP11184554|2011-10-10| EP11184553.3|2011-10-10| EP12171379|2012-06-08| EP12171379.6|2012-06-08| PCT/EP2012/063217|WO2013007619A1|2011-07-08|2012-07-06|Metallocene-catalyzed polyethylene| 相关专利
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