Recyclate based Thermoforming Composition Field of Invention The present invention concerns upgraded polypropylene polyethylene compositions suitable for thermoforming. Background Mixtures of polypropylene and polyethylene such as found in commercially available recyclates are characterized by limited miscibility. When processing such mixtures into final products, the mechanical and optical properties limit the possible applications to non-demanding ultra-low-cost applications, i.e. not an application such as demanding thermoforming. Particularly, the temperature stability of recyclates is usually inappropriate. The attempt has been made of addressing those issues at least in part by super-complex methods such as described in KR10-2184015 using calcium carbonate and special additives. It is also known from WO20190224129 that a recycled component A, (most) preferably with a MFR of 8 to 12 g/10min can be blended with a virgin polypropylene component B having a (most) preferred MFR2 of 0.3 to 0.5 g/10min. Component B can be a random propylene copolymer. However further compositions addressing the needs such as flowability, stiffness, impact strength, and heat distortion temperature as well as vicat in an even better way are required. There is particularly a need for having high heat distortion temperature and high VICAT for given CRYSTEX C2(CF) and also CRYSTEX IV(SF) values. Summary of the Invention The present invention provides A polypropylene-polyethylene composition having ^ a melt flow rate MFR2 (230°C, ISO1133) of 1.5 to 4.0 g/10min, and ^ a tensile modulus of at least 1300 MPa, (measured according to ISO 527-2); and ^ a crystalline fraction (CF) measured according to Crystex analysis preferably as described in the specification, present in an amount in the range from 90.8 to 93.5 wt.-% with respect to the total weight of the polypropylene-polyethylene composition; and ^ a soluble fraction (SF) measured according to Crystex analysis preferably as described in the specification, present in an amount in the range from 6.5 to 9.2 wt.- % with respect to the total weight of the polypropylene-polyethylene composition; and ^ an intrinsic viscosity of the crystalline fraction [IV(CF)], measured according to Crystex analysis preferably as described in the specification, in the range from 2.3 to 2.9 dl/g; and ^ an intrinsic viscosity of the soluble fraction [IV(SF)], measured according to Crystex analysis preferably as described in the specification of 1.80 dl/g to 2.40 dl/g; and ^ a content of units derived from ethylene in the crystalline fraction [C2(CF)] measured according to Crystex analysis preferably as described in the specification in the range of 3.0 to 4.8 wt.%, whereby said polypropylene-polyethylene composition contains a recyclate fraction. The present invention further provides a process of blending for obtaining a polypropylene-polyethylene composition a) 39 to 70 wt.-%, preferably 49 to 70 wt.-% of a recycled polypropylene- polyethylene blend (A) having ^ a crystalline fraction (CF) measured according to Crystex analysis preferably as described in the specification, present in an amount in the range from 89.0 to 92.0 wt.-% with respect to the total weight of the recycled polypropylene- polyethylene blend (A); and ^ a soluble fraction (SF) measured according to Crystex analysis preferably as described in the specification, present in an amount in the range from 8.0 to 11.0 wt.-% with respect to the total weight of the recycled polypropylene-polyethylene blend (A); and ^ an intrinsic viscosity of the crystalline fraction [IV(CF)], measured according to Crystex analysis preferably as described in the specification, in the range from 1.50 to 1.80 dl/g; and ^ an intrinsic viscosity of the soluble fraction [IV(SF)], measured according to Crystex analysis preferably as described in the specification of 0.80 dl/g to 1.80 dl/g; and ^ a content of units derived from ethylene in the crystalline fraction [C2(CF)] measured according to Crystex analysis preferably as described in the specification in the range of 4.0 to 8.0 wt.%, with b) 30 to 61 wt.-%, preferably 30 to 51 wt.-% of a virgin heterophasic propylene copolymer having ^ a melt flow rate MFR ₂ (230°C, ISO1133) of 0.15 to 0.35 g/10min, and ^ a Young’s modulus of at least 1800 MPa determined in tensile testing according to ISO 527-2 on injection molded multi-purpose specimens prepared in accordance with ISO 527-1; and ^ a content of soluble fraction (SF), measured according to Crystex analysis preferably as described in the specification, within the range from 3.0 to 8.0 wt.- %, and based on the total weight of the virgin heterophasic propylene copolymer; and ^ a total ethylene (C2) content, measured according to Crystex analysis preferably as described in the specification, from 0.5 to 3.0 wt.-% based on the total weight of the virgin heterophasic propylene copolymer; all amounts with respect to the final resulting polypropylene-polyethylene composition. The present invention further concerns a thermoformed article made from the polypropylene-polyethylene composition as described herein. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which the invention pertains. Although, any methods and materials similar or equivalent to those described herein can be used in practice for testing of the present invention, the preferred materials and methods are described herein. In describing and claiming the present invention, the following terminology will be used in accordance with the definitions set out below. Unless clearly indicated otherwise, use of the terms “a,” “an,” and the like refers to one or more. For the purposes of the present description, the term “recyclate fraction”, “recyclate” or “recycled” is used to indicate a material recovered from both post-consumer waste and industrial waste, as opposed to virgin polymers. Post-consumer waste refers to objects having completed at least a first use cycle (or life cycle), i.e. having already served their first purpose; while industrial waste refers to manufacturing scrap, which does not normally reach a consumer. The term “virgin” denotes the newly produced materials and/or objects prior to their first use, which have not already been recycled. Virgin materials and recycled materials easily can be differentiated based on absence or presence of contaminants such as limonene content, fatty acid content, polyamide content, polystyrene content, talc content and/or chalk content. “Recyclate fraction” or “recyclate” denote fractions or materials containing residual amounts of limonene, fatty acids, polyamide, polystyrene, talc and/or chalk. “Residual content” denotes a content above the detection limit. A polymer blend is a mixture of two or more polymeric components. It is self explaining that recyclates are nasty mixtures of countless polymers. CRYSTEX analysis yields excellent and quick information as regards the amount of soluble fraction (SF), amount of crystalline fraction (CF), as well as intrinsic viscosities thereof [IV(SF)]; [IV(CF)]. Calibration also allows to provide the amount of units derived from ethylene in the soluble fraction (SF) as well as in the crystalline fraction (CF), i.e. C2(SF) and C2(CF) respectively. Stating “measured according to Crystex analysis preferably as described in the specification” is to be understood as a reference to the experimental section and particularly the test methods. The polypropylene-polyethylene composition according to the present invention preferably has a content of units derived from ethylene measured according to Crystex analysis preferably as described in the specification in the soluble fraction [C2(SF)] of 18.0 to 26.0 wt.%. The polypropylene-polyethylene composition as described herein further has one or more of the following: (i) a content of limonene as determined by using solid phase microextraction (HS-SPME-GC-MS) of from 0.1 ppm to 100 ppm, (ii) a content of fatty acid(s) as determined by using solid phase microextraction (HS-SPME-GC-MS) of 0.1 to 100 ppm (iii) a content of polyamide(s) as determined by IR of 0.001 to 0.5 wt.-%; (iv) a content of polystyrene(s) as determined by IR of 0.05 to 0.8 wt.-%; (v) a content of talc as determined by IR of 0.01 to 0.5 wt.-%; (vi) a content of chalk as determined by IR of 0.01 to 0.5 wt.-%. It goes without saying those contaminants result from the use of the polymers in their “first life”: In other words, features (i) to (vi) indicate recyclate nature. This is particularly true for (i) and (ii) since such contaminants are not used in any virgin material. In a preferred aspect, the polypropylene-polyethylene composition according to the present invention has ^ a tensile modulus of at least 1500 MPa, (measured according to ISO 527-2); and ^ an intrinsic viscosity of the soluble fraction [IV(SF)], measured according to Crystex analysis preferably as described in the specification of 1.95 dl/g to 2.40 dl/g; and ^ a content of units derived from ethylene in the crystalline fraction [C2(CF)] measured according to Crystex analysis preferably as described in the specification in the range of 3.0 to 3.9 wt.%. In yet another preferred aspect, the polypropylene-polyethylene composition according to the present invention has ^ a content of units derived from ethylene in the soluble fraction [C2(SF)] measured according to Crystex analysis preferably as described in the specification of 22.0 to 26.0 wt.%. The polypropylene-polyethylene composition as described herein is preferably obtainable by blending a) 39 to 70 wt.-%, preferably 49 to 70 wt.-% of a recycled polypropylene- polyethylene blend (A) having ^ a crystalline fraction (CF) measured according to Crystex analysis preferably as described in the specification, present in an amount in the range from 89.0 to 92.0 wt.-% with respect to the total weight of the recycled polypropylene- polyethylene blend (A); and ^ a soluble fraction (SF) measured according to Crystex analysis preferably as described in the specification, present in an amount in the range from 8.0 to 11.0 wt.-% with respect to the total weight of the recycled polypropylene- polyethylene blend (A); and ^ an intrinsic viscosity of the crystalline fraction [IV(CF)], measured according to Crystex analysis preferably as described in the specification, in the range from 1.50 to 1.80 dl/g; and ^ an intrinsic viscosity of the soluble fraction [IV(SF)], measured according to Crystex analysis preferably as described in the specification of 0.80 dl/g to 1.80 dl/g; and ^ a content of units derived from ethylene in the crystalline fraction [C2(CF)] measured according to Crystex analysis preferably as described in the specification in the range of 4.0 to 8.0 wt.%, and optionally ^ a percentage of polyethylene melting enthalpy of lower than 2.5 %, preferably lower than 2.1 %; with b) 30 to 61 wt.-%, preferably 30 to 51 wt.-% of a virgin heterophasic propylene copolymer having ^ a melt flow rate MFR2 (230°C, ISO1133) of 0.15 to 0.35 g/10min, and ^ a Young’s modulus of at least 1800 MPa determined in tensile testing according to ISO 527-2 on injection molded multi-purpose specimens prepared in accordance with ISO 527-1, and ^ a content of soluble fraction (SF), measured according to Crystex analysis preferably as described in the specification, within the range from 3.0 to 8.0 wt.- %, and based on the total weight of the virgin heterophasic propylene copolymer, and ^ a total ethylene (C2) content, measured according to Crystex analysis preferably as described in the specification, from 0.5 to 3.0 wt.-% based on the total weight of the virgin heterophasic propylene copolymer, all amounts with respect to the final resulting polypropylene-polyethylene composition. Recycled polypropylene-polyethylene blends (A) as required are commercially available. It is further possible to screen several commercial recyclate products and to prepare intermediate blends in order to meet the requirements. The recycled polypropylene-polyethylene blend (A) is obtained from recycled waste stream of either recycled post-consumer waste or post-industrial waste, such as for example from the automobile industry, or alternatively, a combination of both. It is particularly preferred that the polypropylene-polyethylene blend (A) consists of recycled post-consumer waste and/or post-industrial waste. In one aspect the polypropylene-polyethylene blend (A) may be a polypropylene (PP) rich material of recycled plastic material that comprises significantly more polypropylene than polyethylene. Recycled waste streams, which are high in polypropylene can be obtained for example from the automobile industry, particularly as some automobile parts such as bumpers are sources of fairly pure polypropylene material in a recycling stream or by enhanced sorting. The polypropylene rich material may be obtained by selective processing, degassing and filtration and/or by separation according to type and colors such as NIR or Raman sorting and VIS sorting. It may be obtained from domestic waste streams (i.e. it is a product of domestic recycling) for example the “yellow bag” recycling system organized under the “Green dot” organization, which operates in some parts of Germany. Preferably, the polypropylene-polyethylene blend (A) is obtained from recycled waste by means of plastic recycling processes known in the art. Polypropylene-polyethylene blends (A) as used herein are commercially available, e.g. from Corepla (Italian Consortium for the collection, recovery, recycling of packaging plastic wastes), Resource Plastics Corp. (Brampton, ON), Steinbeis PolyVert, Plastics and Recycling (AT), Vogt Plastik GmbH (DE), Mtm Plastics GmbH (DE) etc. None exhaustive examples of polypropylene rich recycled materials include: Dipolen®PP, Purpolen®PP (Mtm Plastics GmbH), Kruplene-C PP (Steinbeis PolyVert), Systalen PP (Systec Plastics GmbH), Axpoly® recycled polypropylene pellets (Axion Ltd) and PolyPropylene Copolymer (BSP Compounds). A particularly suitable polypropylene- polyethylene blend (A) is “Kruplene-C chalk white 10.1-15.0” which may also be marketed as “Steinbeis rPP” or “Steinbeis rPP C chalk white 10.1-15.0” by Steinbeis Polyvert. Virgin heterophasic propylene copolymers as blend partner required herein are also commercially available. A preferred virgin heterophasic propylene copolymer is Borealis BA2000. It is particularly preferred that said virgin heterophasic propylene copolymer has a Charpy notched impact strength (1eA) (non-instrumented, ISO 179-1 at +23 °C) of at least 27 kJ/m². Preferentially the Charpy notched impact strength (1eA) (non- instrumented, ISO 179-1 at +23 °C) is within the range of 28 to 34 kJ/m². The preferred polypropylene-polyethylene composition as described above is obtainable by blending a) 39 to 70 wt.-%, preferably 49 to 70 wt.-% of a recycled polypropylene- polyethylene blend (A) having ^ a crystalline fraction (CF) measured according to Crystex analysis preferably as described in the specification, present in an amount in the range from 89.0 to 90.7 wt.-% with respect to the total weight of the recycled polypropylene- polyethylene blend (A); and ^ a soluble fraction (SF) measured according to Crystex analysis preferably as described in the specification, present in an amount in the range from 9.3 to 11.0 wt.-% with respect to the total weight of the recycled polypropylene- polyethylene blend (A); and ^ an intrinsic viscosity of the soluble fraction [IV(SF)], measured according to Crystex analysis preferably as described in the specification of 1.60 dl/g to 1.80 dl/g; and ^ a content of units derived from ethylene in the crystalline fraction [C2(CF)] measured according to Crystex analysis preferably as described in the specification in the range of 4.0 to 4.7 wt.%, and optionally ^ a percentage of polyethylene melting enthalpy of lower than 2.1 %; with b) 30 to 61 wt.-%, preferably 30 to 51 wt.-% of a virgin heterophasic propylene copolymer having ^ a melt flow rate MFR2 (230°C, ISO1133) of 0.15 to 0.35 g/10min, and ^ a Young’s modulus of at least 1800 MPa determined in tensile testing according to ISO 527-2 on injection molded multi-purpose specimens prepared in accordance with ISO 527-1; and ^ a Charpy notched impact strength (1eA) (non-instrumented, ISO 179-1 at +23 °C) of at least 27 kJ/m², and ^ a content of soluble fraction (SF), measured according to Crystex analysis preferably as described in the specification, within the range from 3.0 to 8.0 wt.- %, and based on the total weight of the virgin heterophasic propylene copolymer; and ^ a total ethylene (C2) content, measured according to Crystex analysis preferably as described in the specification, from 0.5 to 3.0 wt.-%, all amounts with respect to the final polypropylene-polyethylene composition. It will be appreciated by those skilled in the art that with respect to the recyclate, i.e. polypropylene-polyethylene blend (A), a) a relatively high amount of crystalline fraction (CF) measured according to Crystex analysis preferably as described in the specification, present in the range from 89.0 to 90.7 wt.-% with respect to the total weight of the recycled polypropylene-polyethylene blend (A); together with b) a rather higher intrinsic viscosity of the soluble fraction [IV(SF)], measured according to Crystex analysis preferably as described in the specification of 1.60 dl/g to 1.80 dl/g; together with c) a rather low content of units derived from ethylene in the crystalline fraction [C2(CF)] measured according to Crystex analysis preferably as described in the specification in the range of 4.0 to 4.7 wt.% are beneficial. Moreover, the polypropylene-polyethylene blend (A) has a percentage of polyethylene melting enthalpy of lower than 2.5 %, preferably lower than 2.1 %, most preferably lower than 2.0 wt.-%. It further will be appreciated by those skilled in the art that said virgin heterophasic propylene copolymer as used herein is featured by a relatively low content of soluble fraction (SF), measured according to Crystex analysis preferably as described in the specification, within the range from 3.0 to 8.0 wt.-%, and is further featured by a relatively low total ethylene (C2) content, measured according to Crystex analysis preferably as described in the specification, from 0.5 to 3.0 wt.-%. In a further preferred aspect, the polypropylene-polyethylene compositions as described herein are further characterized by the following inequations: -1.96 * C2(CF) [in wt.-%] + 12.13 * IV(SF) [in dl/g] > 96 and/or -0.32 * C2(CF) [in wt.-%] + 9.5 * IV(SF) [in dl/g] > 151.5 In yet a further aspect, the present invention concerns a process of blending for obtaining a polypropylene-polyethylene composition a) 39 to 70 wt.-%, preferably 49 to 70 wt.-% of a recycled polypropylene- polyethylene blend (A) having ^ a crystalline fraction (CF) measured according to Crystex analysis preferably as described in the specification, present in an amount in the range from 89.0 to 92.0 wt.-% with respect to the total weight of the recycled polypropylene- polyethylene blend (A); and ^ a soluble fraction (SF) measured according to Crystex analysis preferably as described in the specification, present in an amount in the range from 8.0 to 11.0 wt.-% with respect to the total weight of the recycled polypropylene- polyethylene blend (A); and ^ an intrinsic viscosity of the crystalline fraction [IV(CF)], measured according to Crystex analysis preferably as described in the specification, in the range from 1.50 to 1.80 dl/g; and ^ an intrinsic viscosity of the soluble fraction [IV(SF)], measured according to Crystex analysis preferably as described in the specification of 0.80 dl/g to 1.80 dl/g; and ^ a content of units derived from ethylene in the crystalline fraction [C2(CF)] measured according to Crystex analysis preferably as described in the specification in the range of 4.0 to 8.0 wt.%, with b) 30 to 61 wt.-%, preferably 30 to 51 wt.-% of a virgin heterophasic propylene copolymer having ^ a melt flow rate MFR2 (230°C, ISO1133) of 0.15 to 0.35 g/10min, and ^ a Young’s modulus of at least 1800 MPa determined in tensile testing according to ISO 527-2 on injection molded multi-purpose specimens prepared in accordance with ISO 527-1; ^ a content of soluble fraction (SF), measured according to Crystex analysis preferably as described in the specification, within the range from 3.0 to 8.0 wt.- %, and based on the total weight of the virgin heterophasic propylene copolymer; and ^ a total ethylene (C2) content, measured according to Crystex analysis preferably as described in the specification, from 0.5 to 3.0 wt.-% based on the total weight of the virgin heterophasic propylene copolymer; all amounts with respect to the final resulting polypropylene-polyethylene composition. Blending will be usually done by use of an extruder in the presence of a stabilizer package such as known in the art. In the process said virgin heterophasic propylene copolymer preferably has a Charpy notched impact strength (1eA) (non- instrumented, ISO 179-1 at +23 °C) of at least 20 kJ/m². All ranges as discussed above with respect to the composition also hold for the process. The virgin heterophasic polypropylene copolymer shall be described in more detail in the following. The virgin heterophasic propylene copolymers comprise as polymer components a polypropylene matrix (M) and an elastomeric copolymer (EPC). In one embodiment, the least one heterophasic propylene copolymer (HECO) includes a propylene homopolymer (PPH) as (semicrystalline) matrix and a propylene-ethylene rubber as elastomeric propylene copolymer (EPC). The polypropylene matrix (M) is preferably a random propylene copolymer or a propylene homopolymer, the latter being especially preferred. The expression “propylene homopolymer relates to a polypropylene that consists of more than 99.5 wt.-%, preferably of more than or at least of 99.7 wt.-% of propylene units. In a preferred embodiment only propylene units are detectable in the propylene homopolymer. The elastomeric propylene copolymer (EPC) comprises units derived from propylene and ethylene and/or C4 to C20 alpha-olefins, more preferably from ethylene and/or C4 to C10 alpha-olefins and most preferably from ethylene, C4, C6 and/or C8 alpha- olefins, e.g. ethylene and, optionally, units derived from a conjugated diene. The virgin heterophasic propylene copolymer preferably has a total ethylene (C2) content, measured according to Crystex analysis preferably as described in the specification, from 0.5 to 3.0 wt.-%, more preferably from 0.9 to 2.5 wt.-%, most preferably from 1.0 to 2.0 wt.-%. The virgin heterophasic propylene copolymer preferably has a content of soluble fraction (SF), measured according to Crystex analysis preferably as described in the specification, within the range 3.0 to 8.0 wt.-%, more preferably 4.0 to 7.0 wt.-%, and most preferably 5.0 to 6.0 wt.-% based on the total weight of the virgin heterophasic propylene copolymer. The soluble fraction (SF) of the virgin heterophasic propylene copolymer preferably has an ethylene content (C2(SF)), measured according to Crystex analysis preferably as described in the specification, in the range from 10.0 to 30.0 wt.-%, more preferably in the range from 15.0 to 25.0 wt.-%, and most preferably in the range from 18.0 to 22.0 wt.-%. The soluble fraction (SF) of the virgin heterophasic propylene copolymer (HECO-1) preferably has an intrinsic viscosity (iV(SF)) of not more than 4.0 dl/g, more preferably in the range of 3.0 to 4.0 dl/g, even more preferably in the range of 3.2 to 3.9 dl/g, such as 3.5 dl/g. The crystalline fraction (CF) of the virgin heterophasic propylene copolymer (HECO-1) preferably has an ethylene content (C2(CF)), measured according to Crystex analysis preferably as described in the specification, in the range from 0.1 to 2.0 wt.-%, more preferably in the range from 0.2 to 1.0 wt.-%, and most preferably in the range from 0.3 to 0.5 wt.-%. It is to be understood that the present polypropylene polyethylene composition may comprise not only one, but two virgin heterophasic propylene copolymers with different melt flow rates. This allows for an adjustment of the melt flow rate of the final polyolefin composition. The at least one virgin heterophasic propylene copolymer has an impact strength (ISO179-1, Charpy 1eA +23°C) of at least 17 kJ/m ² , more preferably at least 19 kJ/m ² , still more preferably of at least 20 kJ/m ² , in particular in a range between 15 and 40 kJ/m ² , more particular in a range between 17 and 38 kJ/m ² , even more particular in a range between 20 and 36 kJ/m ² . The virgin heterophasic propylene copolymer may have a tensile Young’s modulus measured according to ISO 527-2 of at least 1800 MPa, preferably at least 1830 MPa, like in the range of 1800 to 2100 MPa, preferably in the range of 1830 to 2050 MPa. The virgin heterophasic propylene copolymer (Heco-1) may preferably have a Yield strength of 30-40 MPa, more preferably of 33-37 MPa and independent thereof preferably a strain-at-break of 40-50 %, more preferably of 44-46%. The present invention further concerns a thermoformed article made from polypropylene-polyethylene composition as described herein. Again all preferred aspects and ranges as disclosed for the composition also hold for the thermoformed article. The thermoformed article made from polypropylene-polyethylene composition as described herein preferably contains the polypropylene-polyethylene composition in an amount of at least 97.0 wt.-% with respect to the article, more preferably at least 98.0 wt.-%, and most preferably at least 98.5 wt.-%. Experimental Section The following Examples are included to demonstrate certain aspects and embodiments of the invention as described in the claims. It should be appreciated by those of skill in the art, however, that the following description is illustrative only and should not be taken in any way as a restriction of the invention. Test Methods a) CRYSTEX Determination of Crystalline and soluble fractions and their respective properties (IV and Ethylene content) The crystalline (CF) and soluble fractions (SF) of the polypropylene (PP) compositions as well as the comonomer content and intrinsic viscosities of the respective fractions were analyzed by use of the Crystex (crystallisation extraction) method. Potential instruments that can be used are Crystex QC or Crystex 42 (Polymer Char; Valencia, Spain). Details of the technique and the method can be found in literature (Ljiljana Jeremic, Andreas Albrecht, Martina Sandholzer & Markus Gahleitner (2020) Rapid characterization of high-impact ethylene–propylene copolymer composition by crystallization extraction separation: comparability to standard separation methods, International Journal of Polymer Analysis and Characterization, 25:8, 581- 596) The crystalline and amorphous fractions are separated through temperature cycles of dissolution at 160°C, crystallization at 40°C and re-dissolution in 1,2,4- trichlorobenzene at 160°C. Quantification of SF and CF and determination of ethylene content (C2) are achieved by means of an integrated infrared detector (IR4) and for the determination of the intrinsic viscosity (IV) an online 2-capillary viscometer is used. IR4 detector is a multiple wavelength detector measuring IR absorbance at two different bands (CH3 stretching vibration (centred at app. 2960 cm ^-1 ) and the CH stretching vibration (2700-3000 cm ^-1 ) that are serving for the determination of the concentration and the Ethylene content in Ethylene-Propylene copolymers. IR4 detector is calibrated with series of 8 EP copolymers with known Ethylene content in the range of 2 wt.-% to 69 wt.-% (determined by 13C-NMR) and each at various concentrations, in the range of 2 and 13mg/ml. To encounter for both features, concentration and ethylene content at the same time for various polymer concentration expected during Crystex analyses the following calibration equations were applied: Conc = a + b*Abs(CH) + c*(Abs(CH))² + d*Abs(CH3) + e*(Abs(CH3)² + f*Abs(CH)*Abs(CH ₃ ) (Equation 1) CH3/1000C = a + b*Abs(CH) + c* Abs(CH3) + d * (Abs(CH3)/Abs(CH)) + e * (Abs(CH3)/Abs(CH))² (Equation 2) The constants a to e for equation 1 and a to f for equation 2 were determined by using least square regression analysis. The CH3/1000C is converted to the ethylene content in wt.-% using following relationship: Wt.-% (Ethylene in EP Copolymers) = 100 - CH3/1000TC * 0.3 (Equation 3) Amount of Soluble fraction (SF) and Crystalline Fraction (CF) are correlated through the XS calibration to the “Xylene Cold Soluble” (XCS) quantity and respectively Xylene Cold Insoluble (XCI) fractions, determined according to standard gravimetric method as per ISO16152. XS calibration is achieved by testing various EP copolymers with XS content in the range 2-31 Wt.-%. A linear calibration curve is used. Intrinsic viscosity (IV) of the parent EP copolymer and its soluble and crystalline fractions are determined with a use of an online 2-capillary viscometer and are correlated to corresponding IV’s determined by standard method in decalin according to ISO 1628-3. Calibration is achieved with various EP PP copolymers with IV = 2-4 dL/g. The determined calibration curve is linear. The samples to be analyzed are weighed out in concentrations of 10mg/ml to 20mg/ml. To avoid injecting possible gels and/or polymers which do not dissolve in TCB at 160°C, like PET and PA, the weighed out sample was packed into a stainless steel mesh MW 0,077/D 0,05mmm. After automated filling of the vial with 1,2,4-TCB containing 250 mg/l 2,6-tert-butyl-4- methylphenol (BHT) as antioxidant, the sample is dissolved at 160°C until complete dissolution is achieved, usually for 60 min, with either constant stirring or gentle shaking. To avoid sample degradation, polymer solution is blanketed with the N2 atmosphere during dissolution. A defined volume of the sample solution is injected into the column filled with inert support where the crystallization of the sample and separation of the soluble fraction from the crystalline part is taking place. This process is repeated two times. During the first injection the whole sample is measured at high temperature, determining the IV[dl/g] and the C2[wt.-%] of the PP composition. During the second injection the soluble fraction (at low temperature) and the crystalline fraction (at high temperature) with the crystallization cycle are measured (Wt.-% SF, Wt.-% C2, IV). b) Amount of “iPP”, “PVC”, “PA”, “PET”, “PS” and “PE” determination by Transmission Infra-Red spectroscopy Sample preparation: All calibration samples and samples to be analyzed are prepared in similar way, on molten pressed plates. Around 2 to 3 g of compounds to be analyzed are molten at 190°C. Subsequently, for 20 seconds 60 to 80 bar pressure is applied in a hydraulic heating press. Next, the samples are cooled down to room temperature in 40 second in a cold press under the same pressure, in order to control the morphology of the compound. The thickness of the plates are controlled by metallic calibrated frame plates 2,5 cm by 2,5 cm, 100 to 200 μm thick (depending MFR from the sample); two plates are produced in parallel at the same moment and in the same conditions. The thickness of each plate is measured before any FTIR measurements; all plates are between 100 to 200 μm thick. To control the plate surface and to avoid any interference during the measurement, all plates are pressed between two double-sided silicone release papers. In case of powder samples or heterogeneous compounds, the pressing process would be repeated three times to increase homogeneity by pressed and cutting the sample in the same conditions as described before. Spectrometer: Standard transmission FTIR spectroscope such as Bruker Vertex 70 FTIR spectrometer is used with the following set-up: • a spectral range of 4000-400 cm ^-1 , • an aperture of 6 mm, • a spectral resolution of 2 cm ^-1 , • with 16 background scans, 16 spectrum scans, • an interferogram zero filling factor of 32 • Norton Beer strong apodisation. Spectrum are recorded and analysed in Bruker Opus software. Calibration samples: As FTIR is a secondary method, several calibration standards were compounded to cover the targeted analysis range, typically from: • 0,2 wt.-% to 2,5 wt.-% for PA • 0,1 wt.-% to 5 wt.-% for PS • 0,2 wt.-% to 2,5 wt.-% for PET • 0,1 wt.-% to 4 wt.-% for PVC The following commercial materials were used for the compounds: Borealis HC600TF as iPP, Borealis FB3450 as HDPE and for the targeted polymers such RAMAPET N1S (Indorama Polymer) for PET, Ultramid® B36LN (BASF) for Polyamide 6, Styrolution PS 486N (Ineos) for High Impact Polystyrene (HIPS), and for PVC Inovyn PVC 263B (under powder form). All compounds are made at small scale in a Haake kneader at a temperature below 265°C and less than 10 minutes to avoid degradation. Additional antioxidant such as Irgafos 168 (3000 ppm) is added to minimise the degradation. Calibration: The FTIR calibration principal is the same for all the components: the intensity of a specific FTIR band divided by the plate thickness is correlated to the amount of component determined by 1H or 13C solution state NMR on the same plate. Each specific FTIR absorption band is chosen due to its intensity increase with the amount of the component concentration and due to its isolation from the rest of the peaks, whatever the composition of the calibration standard and real samples. This methodology is described in the publication from Signoret and al. “Alterations of plastic spectra in MIR and the potential impacts on identification towards recycling”, Resources, conservation and Recycling journal, 2020, volume 161, article 104980. The wavelength for each calibration band is: • 3300 cm ^-1 for PA, • 1601 cm ^-1 for PS, • 1410 cm ^-1 for PET, • 615 cm ^-1 for PVC, • 1167 cm ^-1 for iPP. For each polymer component i, a linear calibration (based on linearity of Beer-Lambert law) is constructed. A typical linear correlation used for such calibrations is given below: where xi is the fraction amount of the polymer component i (in wt.-%) Ei is the absorbance intensity of the specific band related to the polymer component i (in a.u. absorbance unit). These specific bands are, 3300 cm ^-1 for PA, 1601 cm ^-1 for PS, 1410 cm ^-1 for PET, 615 cm ^-1 for PVC, 1167 cm ^-1 for iPP d is the thickness of the sample plate Ai and Bi are two coefficients of correlation determined for each calibration curve No specific isolated band can be found for C2 rich fraction and as a consequence the C2 rich fraction is estimated indirectly, ^ଶ ^^^^ ^^^ ^^ ^ௌ ^ா் ா^^ ^^^ ^^^^^ ௧^^^ The EVA, Chalk and Talc contents are estimated “semi-quantitatively”. Hence, this renders the C2 rich content “semi-quantitative”. The following bands are used to estimate the EVA, Chalk and Talc contents: EVA: band centred at 607 cm ^-1 Chalk : band centred at 1798 cm ^-1 Talc : band centred at 3676 cm ^-1 In addition, the presence of titanium di-oxide, TiO2 and Carbon Black are reported. Their quantifications are not feasible with FTIR. For each calibration standard, wherever available, the amount of each component is determined by either ¹ H or ¹³ C solution state NMR, as primary method (except for PA). The NMR measurements are performed on the exact same FTIR plates used for the construction of the FTIR calibration curves. c) Quantification of microstructure by NMR spectroscopy Quantitative nuclear-magnetic resonance (NMR) spectroscopy was used to quantify the ethylene content of the polymers. Quantitative ¹³ C{ ¹ H} NMR spectra were recorded in the solution-state using a Bruker Avance Neo 400 NMR spectrometer operating at 400.15 and 100.62 MHz for ¹ H and ¹³ C respectively. All spectra were recorded using a ¹³ C optimised 10 mm extended temperature probehead at 125°C using nitrogen gas for all pneumatics. Approximately 200 mg of material was dissolved in approximately 3 ml of 1,2- tetrachloroethane-d ₂ (TCE-d ₂ ) along with approximately 3 mg BHT (2,6-di-tert-butyl- 4-methylphenol CAS 128-37-0) and chromium-(III)-acetylacetonate (Cr(acac) ₃ ) resulting in a 60 mM solution of relaxation agent in solvent as described in G. Singh, A. Kothari, V. Gupta, Polymer Testing 2009, 28(5), 475. To ensure a homogenous solution, after initial sample preparation in a heat block, the NMR tube was further heated in a rotatory oven for at least 1 hour. Upon insertion into the magnet the tube was spun at 10 Hz. This setup was chosen primarily for the high resolution and quantitatively needed for accurate ethylene content quantification. Standard single-pulse excitation was employed without NOE, using an optimised tip angle, 1 s recycle delay and a bi-level WALTZ16 decoupling scheme as described in Z. Zhou, R. Kuemmerle, X. Qiu, D. Redwine, R. Cong, A. Taha, D. Baugh, B. Winniford, J. Mag. Reson.187 (2007) 225 and V. Busico, P. Carbonniere, R. Cipullo, C. Pellecchia, J. Severn, G. Talarico, Macromol. Rapid Commun.2007, 28, 1128. A total of 6144 (6k) transients were acquired per spectra. Quantitative ¹³ C{ ¹ H} NMR spectra were processed, integrated and relevant quantitative properties determined from the integrals. All chemical shifts were indirectly referenced to the central methylene group of the ethylene block (EEE) at 30.00 ppm using the chemical shift of the solvent. This approach allowed comparable referencing even when this structural unit was not present. Characteristic signals corresponding to the incorporation of ethylene were observed (as described in Cheng, H. N., Macromolecules 1984, 17, 1950) and the comonomer fraction calculated as the fraction of ethylene in the polymer with respect to all monomer in the polymer: fE = ( E / ( P + E )) The comonomer fraction was quantified using the method of W-J. Wang and S. Zhu, Macromolecules 2000, 331157, through integration of multiple signals across the whole spectral region in the ¹³ C{ ¹ H} spectra. Integral regions were slightly adjusted to increase applicability across the whole range of encountered comonomer contents. The mole percent comonomer incorporation was calculated from the mole fraction: E [mol%] = 100 * fE The weight percent comonomer incorporation was calculated from the mole fraction: E [wt.-%] = 100 * ( fE * 28.06 ) / ( (fE * 28.06) + ((1-fE) * 42.08) ) d) Heat Deflection Temperature (HDT) ISO 75 – method B: The HDT was determined according to ISO 75 method B on specimens of 80 mm ×10 mm × 4 mm. Test specimens were injection moulded according to ISO 19069-2. The specimen were loaded in a three point bending set-up. The specimens are loaded aiming to an outer fibre stress of 0.45 MPa. The temperature is raised with a constant heating rate of 120 °C/h until an outer fibre strain reached 0.2 %. That temperature corresponding this deformation is the heat deflection temperature. e) Vicat Softening Temperature (Method A - 50) The Vicat softening temperature (VST) test was conducted according to ISO 306 method A50 using a load of 10 N and a heating rate of 50 °C /h. The test specimens had a dimension of 10 mm × 10 mm × 4 mm. Type B bars (ISO 20753) 80 mm x 10 mm x 4 mm were injection moulded according to ISO 19069-2. The specimens were milled from the centre of Type B bars to the final dimensions. f) Production of multipurpose specimens (MPS) and Charpy Type 1 specimen All MPS were produced via injection molding according to ISO 3167 (Plastics — Multipurpose test specimens) and ISO 19069-2 (Plastics — Polypropylene (PP) moulding and extrusion materials — Part 2: Preparation of test specimens and determination of properties) on an Engel Victory 60 (Engel, Austria). Specimens were conditioned at 23 °C and 50 % relative humidity for at least three days. After conditioning, these specimens were used for tensile testing. Type 1 specimens for Charpy notched impact testing were prepared via injection moulding according to ISO 19069-2:2016 and also conditioned at 23 °C and 50 % relative humidity for at least three days before testing. g) Melt flow rate (MFR) The MFR measurements were conducted at 230 °C and with 2.16 kg on a Zwick/Roell Mflow melt flow indexer (Zwick Roell, Germany) according to ISO 1133-1 (Plastics - Determination of the melt mass-flow rate (MFR) and melt volume-flow rate (MVR) of thermoplastics - Part 1: Standard method). Cuts were made every 3 mm piston movement. The time between cuts was measured and each extrudate was weighted on an ABS 220-4 electronic balance (Kern & Sohn, Germany). The extrapolation to 10 minutes calculated the MFR in g/10 min for each cut. For each material, one measurement was conducted. Within one measurement, 6 cuts were made and used for the calculation of average values and standard deviations. h) Density The density measurements were conducted according to ISO 01183-1 (Plastics - Methods for determining the density of non-cellular plastics - Part 1: Immersion method, liquid pycnometer method and titration method) with a Sartorius CPA 225D lab balance (Sartorius, Germany). Samples were cut from the sprue-sided shoulders of multi-purpose specimens (MPS). In the first step, the respective sample was weighed dry, measuring its mass in air (m _S,A ). In the second step, the sample was immersed in deionized water with added detergent and put below a buoyancy cage which was connected to the scale, enabling the measurement of the sample buoyancy (mS.IL) without the need of a sinker. A wire was used to free the sample of air bubbles and the temperature of the immersion liquid was recorded for the calculation of its density (ρIL). The sample density was calculated according to following formula with measurement apparatus correction variables A and B: For each material, five samples, each cut from an individual MPS, were used for the calculation of average values and standard deviations. i) Differential scanning calorimetry (DSC) DSC tests were carried out on a Perkin Elmer differential scanning calorimeter DSC 8500 (PerkinElmer, USA). Samples were cut from shoulders of injection molded multi-purpose specimens and encapsuled in perforated aluminum pans. The average sample weight was around 5 mg. The procedure consisted of a first heating, subsequent cooling, and a second heating phase, each in the temperature range of 0 °C to 200 °C with a constant heating/cooling rate of 10 K/min with nitrogen as purge gas and a flow rate of 20 ml/min. The DSC measurements were accomplished to determine the melting peak in the second heat-up phase which is characteristic for the semi-crystallinity achieved under controlled cooling in the DSC device. To determine the melting enthalpy, the area of the melting peak was integrated. Due to the normalization of the heat flux via the specimen mass the thermogram can be shown as normalized heat flux (W/g) over time (s) and the area of the peak (W/g * s) will calculate to W*s/g or J/g normalized melting enthalpy. For each material, five samples, each cut from an individual MPS, were used for the calculation of average values and standard deviations. Measurements were made according to ISO 11357- 1 (Plastics – Differential scanning calorimetry (DSC) – Part 1: General principles) and ISO 11357-3 (Part 3: Determination of temperature and enthalpy of melting and crystallization). In short, the area of the melting peak in the second heating run was integrated. The percentage of polyethylene melting enthalpy is calculated as follows: Percentage of PE melting enthalpy (%) = 100 * PE melting enthalpy / (PE melting enthalpy + PP melting enthalpy). j) Oxidation induction temperature (T _OX ) A differential thermal analysis (DTA) instrument of the type DSC 4000 (PerkinElmer, USA) was utilized to characterize the oxidation induction temperature (dynamic OIT) according to ISO 11357-6 (Plastics – Differential scanning calorimetry (DSC) – Part 6: Determination of oxidation induction time (isothermal OIT) and oxidation induction temperature (dynamic OIT)). Samples were cut from shoulders of injection molded MPS and encapsuled in perforated aluminum pans. The average sample weight was around 5 mg. A single heating step between 23 °C and 300 °C was performed with a heating rate of 10 K/min with synthetic air as purge gas and a flow rate of 20 ml/min. The point of intersect of the slope before oxidation and during oxidation gives the onset of oxidation or the oxidation induction temperature in °C. For each material, five samples, each cut from an individual MPS, were used for the calculation of average values and standard deviations. k) Tensile properties The mechanical properties (Young’s modulus, yield strength and strain at break) were examined with a universal testing machine Zwick AllroundLine Z020 (Zwick Roell, Germany) equipped with a multi-extensometer at 23 °C. Test parameters and MPS were used according to ISO 527-1 (Plastics – Determination of tensile properties – Part 1: General principles) and ISO 527-2 (Part 2: Test conditions for moulding and extrusion plastics) with a traverse speed of 1 mm/min for Young’s modulus determination until a strain of 0.25 % and after that 50 mm/min until failure. For each material five MPS were tested for the calculation of average values and standard deviations. l) Charpy notched impact strength Impact tests were conducted according to ISO 179-1 (Plastics – Determination of Charpy impact properties – Part 1: Non-instrumented impact test) on a Zwick/Roell HIT25P pendulum impact tester (Zwick Roell, Germany) with injection molded specimens (see information below). After pretests to determine the suitable pendulum size, appropriate pendulums were chosen for testing each respective material. Notches were produced with a Leica RM2265 microtome (Leica, Germany) and measured on an Olympus SZX16 stereomicroscope (Olympus, Japan). Test conditions were 23 °C with edgewise notched specimens with 0.25 mm notch-radius (1eA). For each material ten specimens were tested for the calculation of average values and standard deviations. m) Limonene Measurement Limonene quantification was carried out using solid phase microextraction (HS- SPME-GC-MS) by standard addition. 50 mg ground samples were weighed into 20 mL headspace vials and after the addition of limonene in different concentrations and a glass-coated magnetic stir bar. The vial was closed with a magnetic cap lined with silicone/PTFE. Micro capillaries (10 pL) were used to add diluted limonene standards of known concentrations to the sample. Addition of 0, 2, 20 and 100 ng equals 0 mg/kg, 0.1 mg/kg, 1mg/kg and 5 mg/kg limonene, in addition standard amounts of 6.6 mg/kg, 11 mg/kg and 16.5 mg/kg limonene were used in combination with some of the samples tested in this application. For quantification, ion-93 acquired in SIM mode was used. Enrichment of the volatile fraction was carried out by headspace solid phase microextraction with a 2 cm stable flex 50/30 pm DVB/Carboxen/PDMS fibre at 60°C for 20 minutes. Desorption was carried out directly in the heated injection port of a GCMS system at 270°C. GCMS Parameters: Column: 30 m HP 5 MS 0.25*0.25 Injector: Splitless with 0.75 mm SPME Liner, 270°C Temperature program: -10°C ( 1 min) Carrier gas: Helium 5.0, 31 cm/s linear velocity, constant flow MS: Single quadrupole, direct interface, 280°C interface temperature Acquisition: SIM scan mode Scan parameter: 20-300 amu SIM Parameter: m/Z 93, 100 ms dwell time n) Total free fatty acid content Fatty acid quantification was carried out using headspace solid phase micro-extraction (HS-SPME-GC-MS) by standard addition. 50 mg ground samples were weighed in 20 mL headspace vial and after the addition of limonene in different concentrations and a glass coated magnetic stir bar the vial was closed with a magnetic cap lined with silicone/PTFE.10 µL Micro-capillaries were used to add diluted free fatty acid mix (acetic acid, propionic acid, butyric acid, pentanoic acid, hexanoic acid and octanoic acid) standards of known concentrations to the sample at three different levels. Addition of 0, 50, 100 and 500 ng equals 0 mg/kg, 1 mg/kg, 2 mg/kg and 10 mg/kg of each individual acid. For quantification ion 60 acquired in SIM mode was used for all acids except propanoic acid, here ion 74 was used. GCMS Parameter: Column: 20 m ZB Wax plus 0.25*0.25 Injector: Split 5:1 with glass lined split liner, 250°C Temperature program: 40°C ( 1 min) @6°C/min to 120°C, @15°C to 245 °C (5 min) Carrier: Helium 5.0, 40 cm/s linear velocity, constant flow MS: Single quadrupole, direct interface, 220°C inter face temperature Acquisition: SIM scan mode Scan parameter: 46-250 amu 6.6 scans/s SIM Parameter: m/z 60,74, 6.6 scans/s Experiments Commercially available polypropylene-polyethylene blends (A) were used. Table 1 provides an overview of the polypropylene-polyethylene blends (A) #1, #2 and #3. Table 1: Overview of polypropylene-polyethylene blends (A) The commercially available virgin heterophasic propylene copolymer (Borealis HECO BA2000) had a MFR ₂ of 0.23 g/10min; a Young’s modulus of 1850 MPa, and Charpy NIS (23°C) of 33 kJ/m², a total amount of ethylene of 1.35 wt.-% and an amount of 5.6 wt.-% CRYSTEX soluble fraction. An overview is given in Table 2. Table 2: properties of virgin heterophasic propylene copolymer The commercially available polypropylene-polyethylene blends (A) #1 to #3 were blended with said commercially available virgin heterophasic propylene copolymer, whereby all blends were compounded with 0.15 wt.-% Irganox 1010 and 0.15 wt.-% Irgafos 168. Table 3 reports the amounts used for the compositions. Table 3: Overview of compositions Table 4 reports parameters as measured on the resulting compositions. Table 4: Overview of compositions as obtained It can be seen that surprisingly high Vicat and particularly high HDT values were obtained for the inventive compositions. Examples IE1, IE3, IE4, and IE5 further showed excellent tensile moduli.