Polymer composition

By mixing thermoplastics with thermosets and glass fibers, and optionally additives, a polymer composition is formed with enhanced recycling and mechanical properties, addressing the recycling challenges of epoxy resin and glass fiber compositions.

WO2026027335A1PCT designated stage Publication Date: 2026-02-05BASF SE
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Patent Information

Application Number
PCT/EP2025/070985
Authority / Receiving Office
WO · WO
Patent Type
Applications
Current Assignee / Owner
Priority Date
2024-07-31
Filing Date
2025-07-22
Publication Date
2026-02-05

AI Technical Summary

Technical Problem

The recycling of epoxy resin and glass fiber compositions is challenging due to their strong connection, leading to high energy consumption and difficulty in recycling, resulting in materials often being burned or deposited, with a significant carbon footprint and low recycling content.

Method used

A method involving the use of thermoplastics to mix and heat a composition comprising thermosets, glass fibers, and optional additives, followed by comminution and conversion to form a polymer composition with improved recycling content and mechanical properties.

Benefits of technology

The method increases the recycling content of glass fibers and thermosets while improving mechanical properties and reducing the carbon footprint of the resulting polymer composition.

✦ Generated by Eureka AI based on patent content.

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Abstract

Herein a specific polymer composition, polymer product(s) and method for producing the same are described.
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Description

[0001]240470 1 Polymer compositionThe use of compositions comprising an epoxy resin as thermoset and glass fibres are widely spread. For example,these compositions are used in wind rotor blades, tubes, construction elements, bikes, cars and ships. However, therecycling of these materials is not easy due to the presence and strong connection of the thermoset and the glassfibres, so that after end of life, these compositions are usually burned or deposited. It is also possible to use these compositions as feedstocks for a gasification and the obtained chemical material can be converted to obtain a polymercomposition. However, this process is very energy consuming and the glass fibres can be hardly recycled via this route.For these reasons, there is a demand for recycling this kind of compositions to obtain a polymer composition or productexhibiting:- increased recycling content of the glass fibres,- increased recycling content of the thermoset,- improved mechanical properties, and- decreased product carbon footprint.This object is at least partially solved by a method comprising the steps:- providing:- one or more thermoplastic(s) TP1, and- a composition C1 comprising:- one or more thermoset(s) TS1,- glass fibres GF1, and- preferably one or more additive(s) A1;- preferably comminuting the composition C1;- mixing and heating a mixture M1 comprising:- the one or more thermoplastic(s) TP1,- the composition C1, and- preferably one or more additive(s) A1,to obtain a polymer composition PC1; and- preferably converting the polymer composition PC1 to obtain a product PRF1.The inventors recognized that surprisingly if the one or more thermoplastic(s) TP1 and the composition C1 are mixed and heated, a polymer composition is obtained exhibiting increased recycling content of the glass fibres, increasedrecycling content of the thermoset, improved mechanical properties, and a decreased product carbon footprint.Further, this object is at least partially solved by a polymer composition PC1 or product PRF1, obtainable by or obtainedby the following method:- providing:- one or more thermoplastic(s) TP1, and- a composition C1 comprising: 240470 2 -one or more thermoset(s) TS1,- glass fibres GF1, and- preferably one or more additive(s) A1;- preferably comminuting the composition C1;- mixing and heating a mixture M1 comprising:- the one or more thermoplastic(s) TP1,- the composition C1, and- preferably one or more additive(s) A1,to obtain a polymer composition PC1; and- preferably converting the polymer composition PC1 to obtain a product PRF1.Further, this object is at least partially solved by a polymer composition PC1 or product PRF1 obtainable by or obtainedby a method described herein.Further, this object is at least partially solved by a polymer composition PC1 or product PRF1, preferably obtainableby or obtained by a method described herein, comprising, preferably consisting of:- one or more thermoplastic(s) TP1,- a composition C1, and- preferably one or more additive(s) A1;wherein the composition C1 comprises, preferably consists of,- one or more thermoset(s) TS1,- glass fibres GF1, and- preferably one or more additive(s) A1.In addition, this object is at least partially solved by a use of a composition C1 comprising:- one or more thermoset(s) TS1,- glass fibres GF1, and- preferably one or more additive(s) A1;as a component and / or as an additive, preferably as a reinforcing agent, in a polymer composition PC1 comprising one or more thermoplastic(s) TP1 and / or in a product PRF1 comprising one or more thermoplastic(s) TP1. In a preferred embodiment, the method comprises the step:- comminuting the composition C1. Thus, the mechanical properties are improved.In a preferred embodiment, in the comminuting step, the composition C1 is comminuted to obtain a composition ex- hibiting an average grain size of 0.1 mm or more, preferably 0.2 mm or more, more preferably 0.3 mm or more, more preferably 0.4 mm or more, more preferably 0.5 mm or more, more preferably 0.7 mm or more, more preferably 1.0mm or more, more preferably 2.0 mm or more, more preferably 3.0 mm or more, more preferably 4.0 mm or more, 240470 3more preferably 5.0 mm or more, more preferably 10.0 mm or more; and / or in the comminuting step, the compositionC1 is comminuted to obtain a composition exhibiting an average grain size of 500.0 mm or less, preferably 400.0 mm or less, more preferably 300.0 mm or less, more preferably 200.0 mm or less, more preferably 100.0 mm or less, more preferably 50.0 mm or less, more preferably 25.0 mm or less, more preferably 20.0 mm or less, more preferably 15.0 mm or less, more preferably 10.0 mm or less, more preferably 5.0 mm or less, more preferably 1.0 mm or less. Thus, the mechanical properties are improved. In a preferred embodiment, in the heating step, the mixture M1 is heated to a temperature of 150 °C or more, preferably 200 °C or more, more preferably 210 °C or more, more preferably 220 °C or more, more preferably 230 °C or more,more preferably 240 °C or more, more preferably 250 °C or more, more preferably 260 °C or more, more preferably270 °C or more, more preferably 280 °C or more; and / or in the heating step, the mixture M1 is heated to a temperatureof 400 °C or less, preferably 320 °C or less, more preferably 300 °C or less, more preferably 290 °C or less, morepreferably 280 °C or less, more preferably 270 °C or less, more preferably 260 °C or less, more preferably 250 °C orless, more preferably 240 °C or less, more preferably 230 °C or less. Thus, the mechanical properties are improved. In a preferred embodiment, in the heating step, the mixture M1 is heated for 30 seconds or more, preferably 1 minute or more, more preferably 5 minutes or more, more preferably 20 minutes or more, more preferably 40 minutes or more, more preferably 60 minutes or more, more preferably 120 minutes or more, more preferably 180 minutes or more; and / or in the heating step, the mixture M1 is heated for 5 hours or less, preferably 4 hours or less, more preferably 3 hours or less, more preferably 2 hours or less, more preferably 1 hours or less, more preferably 50 minutes or less, more preferably 30 minutes or less, more preferably 10 minutes or less, more preferably 5 minutes or less. Thus, the mechanical properties are improved. In a preferred embodiment, the method comprises the step:- converting the polymer composition PC1 to obtain a product PRF1.In a preferred embodiment, the method comprises the step:- recycling the product PRF1 to obtain a product PRF1’.In a preferred embodiment, the product PRF1 and / or product PRF1’ is / are selected from:i) building block or monomer; orii) polymer, preferably polymer A, polymer composition, preferably polymer composition A, or polymer product,preferably polymer product A; oriii) cleaning polymer, cleaning surfactant, descaling compound, cleaning biocide or composition or formulationthereof; oriv) agrochemical composition, agrochemical formulation auxiliary or agrochemically active ingredient; orv) active pharmaceutical ingredient or intermediate thereof, pharmaceutical excipient, animal feed additive, humanfood additive, dietary supplements, aroma chemical or aroma composition; or 240470 4vi) aqueous polymer dispersion, preferably polyurethane or polyurethane – poly(meth)acrylate hybrid polymer dis-persion, emulsion, binder for paper and fibre coatings, UV-curable acrylic polymer for hot melts and coatings polyisocyanates, hyperbranched polyester polyol, polymeric dispersant for inorganic binder compositions, un- saturated polyester polyol or 100% curable composition; orvii) cosmetic surfactant, emollient, wax, cosmetic polymer, UV filter, further cosmetic ingredient or composition orformulation thereof; orviii) polymer B, polymer composition B, coating composition, other functional composition, foil, molded body, coatingor coated substrate. In a preferred embodiment, the content of the composition C1 in the polymer composition PC1 and / or product PRF1 and / or product PRF1’ is 1 weight-% or more, preferably 2 weight-% or more, more preferably 5 weight-% or more, more preferably 15 weight-% or more, more preferably 30 weight-% or more, more preferably 40 weight-% or more, more preferably 60 weight-% or more, more preferably 80 weight-% or more, more preferably 90 weight-% or more, more preferably 95 weight-% or more; and / or the content of the composition C1 in the polymer composition PC1 and / or product PRF1 and / or product PRF1’ is 99 weight-% or less, preferably 95 weight-% or less, more preferably 90 weight-% or less, more preferably 50 weight-% or less, more preferably 25 weight-% or less, more preferably 10 weight-% or less; and preferably wherein the content is determined based on identity preservation and / or segregation and / or mass balance and / or book and claim chain of custody models, preferably based on mass balance, preferably the International Sus- tainability and Carbon Certification (ISCC) standard. In a preferred embodiment, the composition C1 comprises 10 weight-% or more, preferably 20 weight-% or more, more preferably 30 weight-% or more, more preferably 40 weight-% or more, more preferably 50 weight-% or more, more preferably 60 weight-% or more, more preferably 70 weight-% or more, more preferably 80 weight-% or more, morepreferably 90 weight-% or more, of one or more thermoset(s) TS1; and / or the composition C1 comprises 99 weight-%or less, preferably 95 weight-% or less, more preferably 90 weight-% or less, more preferably 85 weight-% or less, more preferably 80 weight-% or less, more preferably 75 weight-% or less, more preferably 70 weight-% or less, morepreferably 65 weight-% or less, more preferably 60 weight-% or less, more preferably 50 weight-% or less, more pref-erably 40 weight-% or less, more preferably 30 weight-% or less, more preferably 20 weight-% or less, more preferably10 weight-% or less, of one or more thermoset(s) TS1. Thus, the recycling content of the thermoset is increased andthe mechanical properties are improved.In a preferred embodiment, the composition C1 comprises 10 weight-% or more, preferably 20 weight-% or more, more preferably 30 weight-% or more, more preferably 40 weight-% or more, more preferably 50 weight-% or more, more preferably 60 weight-% or more, more preferably 70 weight-% or more, more preferably 80 weight-% or more, morepreferably 90 weight-% or more, of the glass fibres GF1; and / or the composition C1 comprises 99 weight-% or less,preferably 95 weight-% or less, more preferably 90 weight-% or less, more preferably 85 weight-% or less, more pref- erably 80 weight-% or less, more preferably 75 weight-% or less, more preferably 70 weight-% or less, more preferably 240470 5 65 weight-% or less, more preferably 60 weight-% or less, more preferably 50 weight-% or less, more preferably 40 weight-% or less, more preferably 30 weight-% or less, more preferably 20 weight-% or less, more preferably 10 weight- % or less, of the glass fibres GF1. Thus, the recycling content of the glass fibres is increased and the mechanical properties are improved. In a preferred embodiment, the composition C1 comprises, preferably consists of, the one or more thermoset(s) TS1,the glass fibres GF1, preferably and the one or more additive(s) A1. Thus, the mechanical properties are improved.In a preferred embodiment, the polymer composition PC1 and / or the polymer product PRF1 and / or product PRF1’comprise(s), preferably consist(s) of, the one or more thermoplastic(s) TP1, the one or more thermoset(s) TS1, theglass fibres GF1, preferably and the one or more additive(s) A1. Thus, the mechanical properties are improved. In a preferred embodiment, the one or more additive(s) A1 is / are selected from fibre(s), antioxidating agent(s), stabi- lizer(s), lubricant(s), mineral(s), colorant(s), pigment(s), dye(s), soot, talc, carbon black, bio additive(s), plasticizer(s), flame retardant(s), synergist(s) for flame retardant(s), blowing agent(s), acid scavenger(s), antistatic agent(s), antibac- terial agent(s), nucleating agent(s), and mixtures thereof. Besides the glass fibres GF1, the composition C1, polymercomposition PC1, the polymer product PRF1 and / or product PRF1’ may comprise further fibres, preferably glass fibres.However, preferably the composition C1, polymer composition PC1, the polymer product PRF1 and / or product PRF1’ do not contain further glass fibres, preferably fibres. In a preferred embodiment, the composition C1 is obtainable by vacuum infusion or pultrusion or resin transfer mould- ing or filament winding, preferably vacuum infusion, of glass fibres GF0, preferably the fibres GF0 and / or the glass fibres GF1 is / are continuous glass fibres. Thus, the composition C1 is particularly suitable as additive in the polymercomposition and / or the polymer product and the mechanical properties are improved.In a preferred embodiment, the composition C1 comprises glass fibres GF1 exhibiting a length of the average grain size of the composition C1, preferably after comminuting. Thus, the mechanical properties are improved. In a preferred embodiment, the glass fibres GF0 and / or the glass fibres GF1 is / are selected from roving, yarn, textile,preferably non woven textile, woven textile, and multiaxial textile; and mixtures thereof, preferably a textile, more pref-erably a multiaxial textile. Thus, the mechanical properties are improved. In a preferred embodiment, the composition C1 exhibits an average grain size of 0.1 mm or more, preferably 0.2 mm or more, more preferably 0.3 mm or more, more preferably 0.4 mm or more, more preferably 0.5 mm or more, more preferably 0.7 mm or more, more preferably 1.0 mm or more, more preferably 2.0 mm or more, more preferably 3.0 mm or more, more preferably 4.0 mm or more, more preferably 5.0 mm or more, more preferably 10.0 mm or more; and / or the composition C1 exhibits an average grain size of 500.0 mm or less, preferably 400.0 mm or less, more preferably 300.0 mm or less, more preferably 200.0 mm or less, more preferably 100.0 mm or less, more preferably 240470 6 50.0 mm or less, more preferably 25.0 mm or less, more preferably 20.0 mm or less, more preferably 15.0 mm or less, more preferably 10.0 mm or less, more preferably 5.0 mm or less, more preferably 1.0 mm or less, more preferably 0.9 mm or less, more preferably 0.8 mm or less, more preferably 0.7 mm or less, more preferably 0.6 mm or less, more preferably 0.5 mm or less, more preferably 0.4 mm or less, more preferably 0.3 mm or less, more preferably 0.2 mm or less, more preferably 0.1 mm or less. Thus, the mechanical properties are improved. In a preferred embodiment, the composition C1 exhibits a granular shape. Thus, the mechanical properties are im- proved. In a preferred embodiment, the composition C1 is or is derived from waste W1, preferably the waste W1 is post-industrial waste and / or post-consumer waste, more preferably the waste W1 comprises, preferably consists of, windrotor blade(s), tube(s), construction element(s), part(s) of a means of transport; preferably bike, car and / or ship; morepreferably wind rotor blade(s). Thus, the recycling contents of the glass fibres and thermoset are increased, the me-chanical properties are improved and the product carbon footprint is decreased.In a preferred embodiment, the mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s) 10 weight-% or more, preferably 20 weight-% or more, more preferably 30 weight-% or more, more preferably 40 weight-% or more, more preferably 50 weight-% or more, more preferably 60 weight-% or more, more preferably 70 weight-% or more, more preferably 80 weight-% or more, more preferably 90 weight-% or more, of the composition C1;and / or the mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s) 99 weight-% or less,preferably 95 weight-% or less, more preferably 90 weight-% or less, more preferably 85 weight-% or less, more pref- erably 80 weight-% or less, more preferably 75 weight-% or less, more preferably 70 weight-% or less, more preferably 65 weight-% or less, more preferably 60 weight-% or less, more preferably 50 weight-% or less, more preferably 40 weight-% or less, more preferably 30 weight-% or less, more preferably 20 weight-% or less, more preferably 10 weight-% or less, of the composition C1. Thus, the recycling content of the glass fibres and thermoset are increased, themechanical properties are improved and the product carbon footprint is decreased.In a preferred embodiment, the mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s)10 weight-% or more, preferably 20 weight-% or more, more preferably 30 weight-% or more, more preferably 40 weight-% or more, more preferably 50 weight-% or more, more preferably 60 weight-% or more, more preferably 70 weight-% or more, more preferably 80 weight-% or more, more preferably 90 weight-% or more, of one or more ther-moset(s) TS1; and / or the mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s) 99weight-% or less, preferably 95 weight-% or less, more preferably 90 weight-% or less, more preferably 85 weight-% or less, more preferably 80 weight-% or less, more preferably 75 weight-% or less, more preferably 70 weight-% or less, more preferably 65 weight-% or less, more preferably 60 weight-% or less, more preferably 50 weight-% or less, more preferably 40 weight-% or less, more preferably 30 weight-% or less, more preferably 20 weight-% or less, more preferably 10 weight-% or less, of one or more thermoset(s) TS1. Thus, the recycling contents of the thermoset is increased, the mechanical properties are improved and the product carbon footprint is decreased. 240470 7 In a preferred embodiment, the mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s) 10 weight-% or more, preferably 20 weight-% or more, more preferably 25 weight-% or more, more preferably 30 weight-% or more, more preferably 40 weight-% or more, more preferably 50 weight-% or more, more preferably 60 weight-% or more, more preferably 70 weight-% or more, more preferably 80 weight-% or more, more preferably 90weight-% or more, of the glass fibres GF1; and / or the mixture M1 and / or the polymer composition PC1 and / or theproduct PRF1 comprise(s) 99 weight-% or less, preferably 95 weight-% or less, more preferably 90 weight-% or less,more preferably 85 weight-% or less, more preferably 80 weight-% or less, more preferably 75 weight-% or less, more preferably 70 weight-% or less, more preferably 65 weight-% or less, more preferably 60 weight-% or less, more pref- erably 50 weight-% or less, more preferably 40 weight-% or less, more preferably 35 weight-% or less, more preferably30 weight-% or less, more preferably 20 weight-% or less, more preferably 10 weight-% or less, of the glass fibresGF1. Thus, the recycling content of the glass fibres is increased, the mechanical properties are improved and the product carbon footprint is decreased. In a preferred embodiment, the mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s) 10 weight-% or more, preferably 20 weight-% or more, more preferably 30 weight-% or more, more preferably 40 weight-% or more, more preferably 50 weight-% or more, more preferably 60 weight-% or more, more preferably 70 weight-% or more, more preferably 80 weight-% or more, more preferably 90 weight-% or more, of the one or morethermoplastic(s) TP1; and / or the mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s)99 weight-% or less, preferably 95 weight-% or less, more preferably 90 weight-% or less, more preferably 85 weight-% or less, more preferably 80 weight-% or less, more preferably 75 weight-% or less, more preferably 70 weight-% or less, more preferably 65 weight-% or less, more preferably 60 weight-% or less, more preferably 50 weight-% or less, more preferably 40 weight-% or less, more preferably 30 weight-% or less, more preferably 20 weight-% or less, more preferably 10 weight-% or less, of the one or more thermoplastic(s) TP1. Thus, the mechanical properties are improved. In a preferred embodiment, the mixture M1 and / or the polymer composition PC1 and / or the product PRF1 exhibit(s) a ratio (weight-% / weight-%) of the one or more thermoplastic(s) TP1 to the composition C1 of 0.1 or more, preferably 0.2 or more, more preferably 0.3 or more, more preferably 0.4 or more, more preferably 0.5 or more, more preferably0.6 or more, more preferably 0.7 or more, more preferably 0.8 or more, more preferably 0.9 or more; and / or the mixtureM1 and / or the polymer composition PC1 and / or the product PRF1 exhibit(s) a ratio (weight-% / weight-%) of the one ormore thermoplastic(s) TP1 to the composition C1 of 0.9 or less, preferably 0.8 or less, more preferably 0.7 or less,more preferably 0.6 or less, more preferably 0.5 or less, more preferably 0.4 or less, more preferably 0.3 or less, more preferably 0.2 or less, more preferably 0.1 or less. Thus, the recycling content of the glass fibres and thermoset are increased the mechanical properties are improved. In a preferred embodiment, the mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s), preferably consists of, in weight-%: 1 to 98, preferably 20 to 90, more preferably 30 to 80, more preferably 40 to 70 the one or more thermoplastic(s) TP1, 1 to 50, preferably 3 to 40, more preferably 5 to 30, more preferably 10 to 20 the one or more thermoset(s) TS1, 240470 8 1 to 70, preferably 10 to 60, more preferably 20 to 50, more preferably 20 to 40 the glass fibres GF1, and 0 to 50, preferably 1 to 40, more preferably 5 to 30, more preferably 10 to 20 the one or more additive(s) A1. Thus, the mechanical properties are improved. In a preferred embodiment, the mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s), preferably consists of, in weight-%: 1 to 99, preferably 20 to 90, more preferably 30 to 80, more preferably 40 to 70 the one or more thermoplastic(s) TP1, 1 to 80, preferably 15 to 70, more preferably 30 to 60, more preferably 40 to 50 the composition C1, and 0 to 50, preferably 1 to 40, more preferably 5 to 30, more preferably 10 to 20 the one or more additive(s) A1. Thus, the mechanical properties are improved. In a preferred embodiment, the polymer composition PC1 and / or the product PRF1 exhibit(s) an E modulus EMRT of 3000 MPa or more, preferably 4000 MPa or more, more preferably 5000 MPa or more, more preferably 6000 MPa or more, more preferably 7000 MPa or more, more preferably 7500 MPa or more, more preferably 8000 MPa or more,more preferably 8500 MPa or more; and / or the polymer composition PC1 and / or the product PRF1 exhibit(s) an Emodulus EMRT of 15000 MPa or less, preferably 14000 MPa or less, more preferably 13000 MPa or less, more pref- erably 12000 MPa or less, more preferably 11000 MPa or less, more preferably 10500 MPa or less, more preferably 10000 MPa or less, more preferably 9500 MPa or less, more preferably 9000 MPa or less. Thus, the mechanical properties are improved. In a preferred embodiment, the polymer composition PC1 and / or the product PRF1 exhibit(s) a tensile strength at yield sM RT of 10 MPa or more, preferably 30 MPa or more, more preferably 50 MPa or more, more preferably 70 MPa or more, more preferably 90 MPa or more, more preferably 100 MPa or more, more preferably 110 MPa or more, morepreferably 120 MPa or more; and / or the polymer composition PC1 and / or the product PRF1 exhibit(s) a tensile strengthat yield sM RT of 250 MPa or less, preferably 200 MPa or less, more preferably 175 MPa or less, more preferably 150 MPa or less, more preferably 140 MPa or less, more preferably 130 MPa or less. Thus, the mechanical properties are improved.In a preferred embodiment, the polymer composition PC1 and / or the product PRF1 exhibit(s) an elongation at breakeBRT of 0.1 % or more, preferably 0.5 % or more, more preferably 1.0 % or more, more preferably 1.5 % or more,more preferably 2.0 % or more, more preferably 2.2 % or more; and / or the polymer composition PC1 and / or the productPRF1 exhibit(s) an elongation at break eBRT of 70 % or less, preferably 60 % or less, more preferably 50 % or less, more preferably 40 % or less, more preferably 30 % or less, more preferably 20 % or less, more preferably 10 % or less, more preferably 5 % or less, more preferably 4 % or less, more preferably 3 % or less, more preferably 2.5 % or less. Thus, the mechanical properties are improved. In a preferred embodiment, the glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length d0.10length of 10 µm or more, preferably 25 µm or more, more preferably 50 µm or more, more preferably 240470 9 75 µm or more, more preferably 100 µm or more; and / or, preferably and, 1000 µm or less, preferably 750 µm or less, more preferably 500 µm or less, more preferably 250 µm or less, more preferably 200 µm or less, more preferably 150 µm or less, more preferably 110 µm or less. Thus, the mechanical properties are improved. In a preferred embodiment, the glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length d0.50length of 10 µm or more, preferably 100 µm or more, more preferably 200 µm or more, more preferably 250 µm or more, more preferably 290 µm or more; and / or, preferably and, 1000 µm or less, preferably 750 µm or less, more preferably 600 µm or less, more preferably 500 µm or less, more preferably 400 µm or less, more preferably 350 µm or less, more preferably 300 µm or less. Thus, the mechanical properties are improved. In a preferred embodiment, the glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length <50µmlengthof 0.5 % or more, preferably 2.0 % or more, more preferably 2.5 % or more, more preferably 3.0 % or more, more preferably 3.4 % or more; and / or, preferably and, 20 % or less, preferably 15 % or less, more preferably 12 % or less, more preferably 10 % or less, more preferably 5.0 % or less, more preferably 4.0 % or less, more preferably 3.6 % or less. Thus, the mechanical properties are improved. In a preferred embodiment, the glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length <100µmlength of 1 % or more, preferably 5 % or more, more preferably 8 % or more, more preferably 9 % or more, more preferably 9.5 % or more; and / or, preferably and, 50 % or less, preferably 30 % or less, more preferably 20 % or less, more preferably 15 % or less, more preferably 12.0 % or less, more preferably 11.0 % or less, more preferably 10.5 % or less. Thus, the mechanical properties are improved. In a preferred embodiment, the glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length <200µmlength of 1 % or more, preferably 10 % or more, more preferably 18 % or more, more preferably 22 % or more, more preferably 26 % or more; and / or, preferably and, 80 % or less, preferably 60 % or less, more preferably 40 % or less, more preferably 35 % or less, more preferably 32 % or less, more preferably 30 % or less, more preferably 28 % or less. Thus, the mechanical properties are improved. In a preferred embodiment, the glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length d0.10frequencyof 1 µm or more, preferably 25 µm or more, more preferably 35 µm or more, more preferably 38 µm or more, more preferably 41 µm or more; and / or, preferably and, 80 µm or less, preferably 70 µm or less, more preferably 60 µm or less, more preferably 50 µm or less, more preferably 48 µm or less, more preferably 45 µm orless, more preferably 43 µm or less. Thus, the mechanical properties are improved.In a preferred embodiment, the glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length d0.50frequency of 10 µm or more, preferably 100 µm or more, more preferably 125 µm or more, more pref- erably 150 µm or more, more preferably 155 µm or more; and / or, preferably and, 1000 µm or less, preferably 750 µm 240470 10 or less, more preferably 500 µm or less, more preferably 400 µm or less, more preferably 200 µm or less, more preferably 180 µm or less, more preferably 170 µm or less. Thus, the mechanical properties are improved. In a preferred embodiment, the glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length <50µmfrequency of 0.5 % or more, preferably 5.0 % or more, more preferably 10.0 % or more, more preferably 12.0 % or more, more preferably 16.0 % or more; and / or, preferably and, 80 % or less, preferably 45 % or less, more preferably 40 % or less, more preferably 35 % or less, more preferably 25 % or less, more preferably 20 % or less, more preferably 18 % or less. Thus, the mechanical properties are improved. In a preferred embodiment, the glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length <100µmfrequencyof 1 % or more, preferably 15 % or more, more preferably 30 % or more, more preferably 32 % or more, more preferably 35 % or more; and / or, preferably and, 80 % or less, preferably 60 % or less, more preferably 50 % or less, more preferably 45 % or less, more preferably 42 % or less, more preferably 40 % or less, more preferably 37 % or less. Thus, the mechanical properties are improved. In a preferred embodiment, the glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length <200µmfrequency of 5 % or more, preferably 35 % or more, more preferably 50 % or more, more preferably 55 % or more, more preferably 57 % or more; and / or, preferably and, 90 % or less, preferably 80 % or less, more preferably 70 % or less, more preferably 65 % or less, more preferably 61 % or less, more preferably 59 % or less. Thus, the mechanical properties are improved.The thermoset is not particularly limited. In a preferred embodiment, the one or more thermoset(s) TS1 is / are an un-saturated polyester and / or an epoxy resin, preferably an epoxy resin. Thus, the mechanical properties are improved.In a preferred embodiment, the one or more thermoset(s) TS1 is / are obtainable by the reaction of component A com-prising one or more monomer(s) comprising one or more epoxide groups and a component B comprising one or more monomer(s) comprising one or more amine group(s), preferably primary amine group(s). Thus, the mechanical prop- erties are improved.In a preferred embodiment, the decomposition temperature of the one or more thermoset(s) TS1 is / are 200 °C or moreand 800°C or less, preferably 300 °C or more and 700 °C or less, more preferably, 350 °C or more and 600 °C or less, more preferably, 400 °C or more and 500 °C or less. Thus, the mechanical properties are improved. In a preferred embodiment, the mixture M1 and / or the polymer composition PC1 and / or the product PRF1 is / are a dispersion comprising particles PR1 comprising the one or more thermoset(s) TS1, preferably and the glass fibres GF1, more preferably the composition C1, and a phase, preferably a continuous phase, comprising the one or more thermoplastic(s) TP1. Thus, the mechanical properties are improved. 240470 11 In a preferred embodiment, the mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s) particles PR1 comprising, preferably consisting of, the one or more thermoset(s) TS1, preferably and the glass fibres GF1, more preferably the composition C1. Thus, the mechanical properties are improved. In a preferred embodiment, the particle(s) PR1 and / or the glass fibres GF1 and / or the composition C1 are at least partially wrapped by the one or more thermoplastic(s) TP1. Thus, the mechanical properties are improved. In a preferred embodiment, the polymer composition PC1 comprises glass fibre GF1 which are at least partially wrapped by the one or more thermoset(s) TS1. Thus, the mechanical properties are improved. In a preferred embodiment, the mixture M1 and / or the polymer composition PC1 and / or the product PRF1 is not ho- mogeneous. Thus, the mechanical properties are improved. In a preferred embodiment, the composition C1 is a free flowing composition. Thus, the mechanical properties are improved. In a preferred embodiment, the composition C1 comprises a bulk density [g / cm3] of 1.0 or more, preferably 1.5 or more,preferably 2.0 or more and / or the composition C1 comprises a bulk density [g / cm3] of 0.9 or more, preferably 1.1 ormore, preferably 1.3 or more, preferably 1.5 or more. Thus, the feeding and mixing of the composition C1 is simplified. As a consequence, the obtained polymer composition is more homogeneous and thus, the mechanical properties are improved. The glass fibres are not particularly limited. In a preferred embodiment, the glass fibres GF1 are long glass fibres,preferably continuous glass fibres. Thus, the mechanical properties are improved.In a preferred embodiment, the component C1 comprises, preferably consists of, continuous glass fibres GF1, and wherein the continuous glass fibres GF1 are assembled to form a unidirectional and multidirectional glass fibres textile and / or the component C1 comprises, preferably consists of, continuous glass fibres GF1, and wherein the continuous glass fibres GF1 are arranged in one or more textile plie(s), and wherein one or more textile plie(s) of the continuous glass fibres GF1 are assembled to reach a multitude of orientations, preferably wherein the one or more textile plies(s) are two or more textile plies(s), more preferably 2 to 200 textile plies(s), more preferably 3 to 50 textile plies(s). Thus, the mechanical properties are improved. In a preferred embodiment, the glass fibres GF1 in the polymer composition PC1 are isotropically distributed. Thus, the mechanical properties are improved. In a preferred embodiment, the glass fibres GF1 form a textile T1 and wherein the textile T1 is a nonwoven textile. Thus, the mechanical properties are improved. 240470 12 In a preferred embodiment, the glass fibres GF1 in the composition C1 are not woven, knitted, braided, or laid. Thus, the mechanical properties are improved.The one or more thermoplastic(s) TP1 is / are not particularly limited. In a preferred embodiment, the one or more ther-moplastic(s) TP1 is / are selected from polyamide, polypropylene, polyethylene, polyester, styrene, polyvinylchloridePVC, polyoxymethylene POM, polyketone, polyether ether ketone PEEK, polyimide and mixtures thereof, preferably isa polyamide. Thus, the mechanical properties are improved.In a preferred embodiment, the polyamide is selected from PA6, PA 66, PA56, PA 610, PA11, PA12, PA1010, PA1012, PPA, PA46; and mixtures and / or copolymers thereof, preferably PA 6, PA 66; and mixtures and / or copolymers thereof; and mixtures thereof, more preferably is PA 6. Thus, the mechanical properties are improved.In a preferred embodiment, the method is a method for the production of a polymer composition and / or a polymerproduct, preferably wherein the polymer composition and / or polymer product exhibit(s) an increased recycling contentof the glass fibres, an increased recycling content of the thermoset, improved mechanical properties, and / or, preferably and, a decreased product carbon footprint. In a preferred embodiment, the product PRF1 is not a wind turbine blade. In a preferred embodiment, the product PRF1’ is not a wind turbine blade.In a preferred embodiment, the composition C1 is not derived from (a) wind rotor blade(s) and / or wind turbine blade(s).In a preferred embodiment, the one or more thermoplastic(s) TP1 is / are not a foam. Thus, the mechanical propertiesare improved. In a preferred embodiment, the one or more thermoplastic(s) TP1 and / or polymer composition PC1 and / or polymer product PRF1 exhibit(s) a density of 0.4 g / cm3or more, preferably 0.6 g / cm3or more, more preferably 0.8 g / cm3or more, more preferably 1.0 g / cm3or more, more preferably 1.2 g / cm3or more; and / or the one or more thermoplastic(s) TP1 and / or polymer composition PC1 and / or polymer product PRF1 exhibit(s) a density of 2.0 g / cm3or less, preferably1.6 g / cm3 or less, more preferably 1.4 g / cm3 or less. Thus, the mechanical properties are improved.In a preferred embodiment, the composition C1 exhibits a sandwich structure, preferably in which glass fibres GF1form the core and the one or more thermoset(s) TS1, preferably and the one or more additive(s) A1, form(s) the skins. Thus, the mechanical properties are improved. 240470 13In a preferred embodiment, in the composition C1, the glass fibres GF1 are held in the one or more thermoset(s) TS1,preferably and the one or more additive(s) A1, by mechanical anchoring and / or chemical adhesion, preferably by acombination of mechanical anchoring and chemical adhesion. Thus, the mechanical properties are improved.In a preferred embodiment, the composition C1 exhibits a layered structure. Thus, the mechanical properties are im-proved.In a preferred embodiment, the composition C1 exhibits a layered structure, in which glass the glass fibres GF1 arepresent as fabric plies, two or more of the fabric plies are laid up together and the one of more thermoset(s) TS1,preferably and the one or more additive(s) A1, are interpenetrated in the fabric plies and between the fabric plies. Thus,the mechanical properties are improved. Methods and Definitions If not stated otherwise, normal conditions are used and / or applied, e.g., room temperature, preferably 25°C, and 1 bar, preferably 1013.25 mbar. If not further specified, preferably the following methods are used and definitions apply: The average grain size was determined according to DIN 66165-2. The decomposition temperature was measured by thermogravimetric analysis, using a TGA Q5000 (TA Instruments). The temperature was increased up to 600°C with a heating ramp of 10K / min under nitrogen atmosphere. The instru-ment determined the weight loss as a function of temperature.The different phases of the dispersion were determined as follow: confocal microscopy CLSM using scattering and fluorescence signals. The samples were prepared via polishing of the surface and application of Neocarmin®as fluo- rescence contrast material.E modulus EM RT, tensile strength at yield sM RT and the elongation at break eB RT were measured according to ISO527-1 at room temperature (=25°C).The bulk density was measured as follows: A 250 mL measuring cylinder is filled with composition C1 until reachingthe 250 ml mark. The weight of the cylinder is measured empty and filled. The difference gives the weight of a volumeof 250 mL composition C1, this value is multiplied by 4 to give the bulk density [g / cm3]. 240470 14The length of the glass fibres was determined as follows: First, the polymer compound comprising the glass fibres waspyrolyzed at 650°C for 1.5 h to obtain the glass fibres. Then, a tip of a spatula (about 5 mg) glass fibres was dispersedin a mixture of 100 mL water and 2 drops of glycerin and transferred to a petri dish, which was placed on the surfaceof an Epson perfection V850 Pro flatbed scanner. Fibres shorter than 21.2 µm cannot be detected due to the limitedresolution of the scanner. Thus, fibres being shorter than 21.2 µm were not considered.Calculation of the values: wherein L50µmlength is the sum of the length (µm) of all fibres GF1 being smaller than 50 µm, andwherein is the sum of the length (µm) of all fibres GF1. wherein L50µmfrequency is the sum of all fibres GF1 being smaller than 50 µm, andwherein the sum of all fibres GF1. wherein L100µmlength is the sum of the length (µm) of all fibres GF1 being smaller than 100 µm, andwherein is the sum of the length (µm) of all fibres GF1. wherein is the sum of all fibres GF1 being smaller than 100 µm, andwherein the sum of all fibres GF1. wherein L200µmlength is the sum of the length (µm) of all fibres GF1 being smaller than 200 µm, andwherein is the sum of the length (µm) of all fibres GF1. wherein is the sum of all fibres GF1 being smaller than 200 µm, andwherein the sum of all fibres GF1. 240470 15 d0.10length: d0.10length = 0.1wherein Llength is the sum of the length (µm) of all fibres GF1.d0.10frequency = maximum length (µm) of 10% of the smallest fibres GF1. wherein is the sum of the length (µm) of all fibres GF1.d0.50frequency= maximum length (µm) of 50% of the smallest fibres GF1. In summary, embodiments and preferred embodiments are the following embodiments. The scope of protection is defined by the claims. The combination of two or more embodiments, e.g.3, 4 or 8 embodiments is further preferred. Definitions and general statements herein preferably also apply for the following embodiments and preferred embodi-ments. In addition, if not stated otherwise, definitions and general statements herein referring the polymer compositionalso apply for the polymer product(s), method and use, and vice versa. Preferably, the steps described in the embodi- ments below are conducted, if present in the claims, in the order of the embodiments below.1. Method comprising the steps, preferably in this order:- providing:- one or more thermoplastic(s) TP1, and- a composition C1 comprising:- one or more thermoset(s) TS1,- glass fibres GF1, and- preferably one or more additive(s) A1;- preferably comminuting the composition C1;- mixing and heating a mixture M1 comprising:- the one or more thermoplastic(s) TP1,- the composition C1, and- preferably one or more additive(s) A1,to obtain a polymer composition PC1; and -preferably converting the polymer composition PC1 to obtain a product PRF1.2. Polymer composition PC1 or product PRF1, obtainable by or obtained by the following method:- providing: 240470 16 -one or more thermoplastic(s) TP1, and- a composition C1 comprising:- one or more thermoset(s) TS1,- glass fibres GF1, and- preferably one or more additive(s) A1;- preferably comminuting the composition C1;- mixing and heating a mixture M1 comprising:- the one or more thermoplastic(s) TP1,- the composition C1, and- preferably one or more additive(s) A1,to obtain a polymer composition PC1; and -preferably converting the polymer composition PC1 to obtain a product PRF1.3. Polymer composition PC1 or product PRF1, preferably according to any one of the preceding embodiments,obtainable by or obtained by a method according to any one of the preceding embodiments.4. Polymer composition PC1 or product PRF1, preferably obtainable by or obtained by a method according to anyone of the preceding embodiments, comprising, preferably consisting of: -one or more thermoplastic(s) TP1,- a composition C1, and- preferably one or more additive(s) A1;wherein the composition C1 comprises, preferably consists of, -one or more thermoset(s) TS1,- glass fibres GF1, and- preferably one or more additive(s) A1.5. Use of a composition C1 comprising:- one or more thermoset(s) TS1,- glass fibres GF1, and- preferably one or more additive(s) A1;as a component and / or as an additive, preferably as a reinforcing agent, in a polymer composition PC1 com- prising one or more thermoplastic(s) TP1 and / or in a product PRF1 comprising one or more thermoplastic(s) TP1.6. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe method comprises the step: -comminuting the composition C1. 240470 177. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, wherein, inthe comminuting step, the composition C1 is comminuted to obtain a composition exhibiting an average grain size of 0.1 mm or more, preferably 0.2 mm or more, more preferably 0.3 mm or more, more preferably 0.4 mm or more, more preferably 0.5 mm or more, more preferably 0.7 mm or more, more preferably 1.0 mm or more,more preferably 2.0 mm or more, more preferably 3.0 mm or more, more preferably 4.0 mm or more, more preferably 5.0 mm or more, more preferably 10.0 mm or more.8. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, wherein, inthe comminuting step, the composition C1 is comminuted to obtain a composition exhibiting an average grain size of 500.0 mm or less, preferably 400.0 mm or less, more preferably 300.0 mm or less, more preferably 200.0 mm or less, more preferably 100.0 mm or less, more preferably 50.0 mm or less, more preferably 25.0 mm or less, more preferably 20.0 mm or less, more preferably 15.0 mm or less, more preferably 10.0 mm or less, more preferably 5.0 mm or less, more preferably 1.0 mm or less.9. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, wherein, inthe heating step, the mixture M1 is heated to a temperature of 150 °C or more, preferably 200 °C or more, more preferably 210 °C or more, more preferably 220 °C or more, more preferably 230 °C or more, more preferably 240 °C or more, more preferably 250 °C or more, more preferably 260 °C or more, more preferably 270 °C ormore, more preferably 280 °C or more.10. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, wherein, inthe heating step, the mixture M1 is heated to a temperature of 400 °C or less, preferably 320 °C or less, more preferably 300 °C or less, more preferably 290 °C or less, more preferably 280 °C or less, more preferably 270 °C or less, more preferably 260 °C or less, more preferably 250 °C or less, more preferably 240 °C or less, more preferably 230 °C or less.11. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, wherein, inthe heating step, the mixture M1 is heated for 30 seconds or more, preferably 1 minute or more, more preferably 5 minutes or more, more preferably 20 minutes or more, more preferably 40 minutes or more, more preferably 60 minutes or more, more preferably 120 minutes or more, more preferably 180 minutes or more.12. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, wherein, inthe heating step, the mixture M1 is heated for 5 hours or less, preferably 4 hours or less, more preferably 3 hours or less, more preferably 2 hours or less, more preferably 1 hours or less, more preferably 50 minutes or less, more preferably 30 minutes or less, more preferably 10 minutes or less, more preferably 5 minutes or less.13. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe method comprises the step: 240470 18 -converting the polymer composition PC1 to obtain a product PRF1.14. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe method comprises the step: -recycling the product PRF1 to obtain a product PRF1’.15. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe product PRF1 and / or product PRF1’ is / are selected from:i) building block or monomer; orii) polymer, preferably polymer A, polymer composition, preferably polymer composition A, or polymer prod-uct, preferably polymer product A; or iii) cleaning polymer, cleaning surfactant, descaling compound, cleaning biocide or composition or formu-lation thereof; or iv) agrochemical composition, agrochemical formulation auxiliary or agrochemically active ingredient; orv) active pharmaceutical ingredient or intermediate thereof, pharmaceutical excipient, animal feed additive,human food additive, dietary supplements, aroma chemical or aroma composition; or vi) aqueous polymer dispersion, preferably polyurethane or polyurethane – poly(meth)acrylate hybrid poly-mer dispersion, emulsion, binder for paper and fibre coatings, UV-curable acrylic polymer for hot melts and coatings polyisocyanates, hyperbranched polyester polyol, polymeric dispersant for inorganic binder compositions, unsaturated polyester polyol or 100% curable composition; or vii) cosmetic surfactant, emollient, wax, cosmetic polymer, UV filter, further cosmetic ingredient or composi-tion or formulation thereof; or viii) polymer B, polymer composition B, coating composition, other functional composition, foil, molded body,coating or coated substrate.16. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe content of the composition C1 in the polymer composition PC1 and / or product PRF1 and / or product PRF1’ is 1 weight-% or more, preferably 2 weight-% or more, more preferably 5 weight-% or more, more preferably 15 weight-% or more, more preferably 30 weight-% or more, more preferably 40 weight-% or more, more preferably60 weight-% or more, more preferably 80 weight-% or more, more preferably 90 weight-% or more, more pref- erably 95 weight-% or more; and / or wherein the content of the composition C1 in the polymer composition PC1 and / or product PRF1 and / or product PRF1’ is 99 weight-% or less, preferably 95 weight-% or less, more preferably 90 weight-% or less, more pref-erably 50 weight-% or less, more preferably 25 weight-% or less, more preferably 10 weight-% or less; and preferably wherein the content is determined based on identity preservation and / or segregation and / or mass balance and / or book and claim chain of custody models, preferably based on mass balance, preferably the International Sustainability and Carbon Certification (ISCC) standard. 240470 1917. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 comprises 10 weight-% or more, preferably 20 weight-% or more, more preferably 30 weight-% or more, more preferably 40 weight-% or more, more preferably 50 weight-% or more, more preferably 60 weight-% or more, more preferably 70 weight-% or more, more preferably 80 weight-% or more, more pref-erably 90 weight-% or more, of one or more thermoset(s) TS1.18. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 comprises 99 weight-% or less, preferably 95 weight-% or less, more preferably 90 weight-% or less, more preferably 85 weight-% or less, more preferably 80 weight-% or less, more preferably 75 weight- % or less, more preferably 70 weight-% or less, more preferably 65 weight-% or less, more preferably 60 weight- % or less, more preferably 50 weight-% or less, more preferably 40 weight-% or less, more preferably 30 weight- % or less, more preferably 20 weight-% or less, more preferably 10 weight-% or less, of one or more thermo- set(s) TS1.19. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 comprises 10 weight-% or more, preferably 20 weight-% or more, more preferably 30 weight-% or more, more preferably 40 weight-% or more, more preferably 50 weight-% or more, more preferably 60 weight-% or more, more preferably 70 weight-% or more, more preferably 80 weight-% or more, more pref- erably 90 weight-% or more, of the glass fibres GF1.20. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 comprises 99 weight-% or less, preferably 95 weight-% or less, more preferably 90 weight-% or less, more preferably 85 weight-% or less, more preferably 80 weight-% or less, more preferably 75 weight- % or less, more preferably 70 weight-% or less, more preferably 65 weight-% or less, more preferably 60 weight- % or less, more preferably 50 weight-% or less, more preferably 40 weight-% or less, more preferably 30 weight- % or less, more preferably 20 weight-% or less, more preferably 10 weight-% or less, of the glass fibres GF1.21. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 comprises, preferably consists of, the one or more thermoset(s) TS1, the glass fibres GF1, preferably and the one or more additive(s) A1.22. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe polymer composition PC1 and / or the polymer product PRF1 and / or product PRF1’ comprise(s), preferablyconsist(s) of, the one or more thermoplastic(s) TP1, the one or more thermoset(s) TS1, the glass fibres GF1,preferably and the one or more additive(s) A1.23. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe one or more additive(s) A1 is / are selected from fibre(s), antioxidating agent(s), stabilizer(s), lubricant(s), 240470 20 mineral(s), colorant(s), pigment(s), dye(s), soot, talc, carbon black, bio additive(s), plasticizer(s), flame retard- ant(s), synergist(s) for flame retardant(s), blowing agent(s), acid scavenger(s), antistatic agent(s), antibacterial agent(s), nucleating agent(s), and mixtures thereof.24. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 is obtainable by vacuum infusion or pultrusion or resin transfer moulding or filament winding, preferably vacuum infusion, of glass fibres GF0.25. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe fibres GF0 and / or the glass fibres GF1 is / are continuous glass fibres.26. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 comprises glass fibres GF1 exhibiting a length of the average grain size of the composition C1, preferably after comminuting.27. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe glass fibres GF0 and / or the glass fibres GF1 is / are selected from roving, yarn, textile, preferably non woven textile, woven textile, and multiaxial textile; and mixtures thereof, preferably a textile, more preferably a multi-axial textile.28. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 exhibits an average grain size of 0.1 mm or more, preferably 0.2 mm or more, more prefer- ably 0.3 mm or more, more preferably 0.4 mm or more, more preferably 0.5 mm or more, more preferably 0.7 mm or more, more preferably 1.0 mm or more, more preferably 2.0 mm or more, more preferably 3.0 mm or more, more preferably 4.0 mm or more, more preferably 5.0 mm or more, more preferably 10.0 mm or more.29. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 exhibits an average grain size of 500.0 mm or less, preferably 400.0 mm or less, more preferably 300.0 mm or less, more preferably 200.0 mm or less, more preferably 100.0 mm or less, more pref- erably 50.0 mm or less, more preferably 25.0 mm or less, more preferably 20.0 mm or less, more preferably 15.0 mm or less, more preferably 10.0 mm or less, more preferably 5.0 mm or less, more preferably 1.0 mm or less, more preferably 0.9 mm or less, more preferably 0.8 mm or less, more preferably 0.7 mm or less, more preferably 0.6 mm or less, more preferably 0.5 mm or less, more preferably 0.4 mm or less, more preferably 0.3 mm or less, more preferably 0.2 mm or less, more preferably 0.1 mm or less.30. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 exhibits a granular shape. 240470 2131. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 is or is derived from waste W1.32. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe waste W1 is post-industrial waste and / or post-consumer waste.33. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe waste W1 comprises, preferably consists of, wind rotor blade(s), tube(s), construction element(s), part(s) ofa means of transport; preferably bike, car and / or ship; more preferably wind rotor blade(s).34. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s) 10 weight-% or more, preferably 20 weight-% or more, more preferably 30 weight-% or more, more preferably 40 weight-% or more, more preferably 50 weight-% or more, more preferably 60 weight-% or more, more preferably 70 weight-% or more, more preferably 80 weight-% or more, more preferably 90 weight-% or more, of the composition C1.35. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s) 99 weight-% or less,preferably 95 weight-% or less, more preferably 90 weight-% or less, more preferably 85 weight-% or less, more preferably 80 weight-% or less, more preferably 75 weight-% or less, more preferably 70 weight-% or less, more preferably 65 weight-% or less, more preferably 60 weight-% or less, more preferably 50 weight-% or less, more preferably 40 weight-% or less, more preferably 30 weight-% or less, more preferably 20 weight-% or less, more preferably 10 weight-% or less, of the composition C1.36. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s) 10 weight-% or more, preferably 20 weight-% or more, more preferably 30 weight-% or more, more preferably 40 weight-% or more, more preferably 50 weight-% or more, more preferably 60 weight-% or more, more preferably 70 weight-% or more, more preferably 80 weight-% or more, more preferably 90 weight-% or more, of one or more thermoset(s) TS1.37. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s) 99 weight-% or less,preferably 95 weight-% or less, more preferably 90 weight-% or less, more preferably 85 weight-% or less, more preferably 80 weight-% or less, more preferably 75 weight-% or less, more preferably 70 weight-% or less, more preferably 65 weight-% or less, more preferably 60 weight-% or less, more preferably 50 weight-% or less, more preferably 40 weight-% or less, more preferably 30 weight-% or less, more preferably 20 weight-% or less, more preferably 10 weight-% or less, of one or more thermoset(s) TS1. 240470 2238. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s) 10 weight-% or more, preferably 20 weight-% or more, more preferably 25 weight-% or more, more preferably 30 weight-% or more, more preferably 40 weight-% or more, more preferably 50 weight-% or more, more preferably 60 weight-% or more, more preferably 70 weight-% or more, more preferably 80 weight-% or more, more preferably 90 weight- % or more, of the glass fibres GF1.39. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s) 99 weight-% or less,preferably 95 weight-% or less, more preferably 90 weight-% or less, more preferably 85 weight-% or less, more preferably 80 weight-% or less, more preferably 75 weight-% or less, more preferably 70 weight-% or less, more preferably 65 weight-% or less, more preferably 60 weight-% or less, more preferably 50 weight-% or less, more preferably 40 weight-% or less, more preferably 35 weight-% or less, more preferably 30 weight-% or less, more preferably 20 weight-% or less, more preferably 10 weight-% or less, of the glass fibres GF1.40. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s) 10 weight-% or more, preferably 20 weight-% or more, more preferably 30 weight-% or more, more preferably 40 weight-% or more, more preferably 50 weight-% or more, more preferably 60 weight-% or more, more preferably 70 weight-% or more, more preferably 80 weight-% or more, more preferably 90 weight-% or more, of the one or more thermo- plastic(s) TP1.41. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s) 99 weight-% or less,preferably 95 weight-% or less, more preferably 90 weight-% or less, more preferably 85 weight-% or less, more preferably 80 weight-% or less, more preferably 75 weight-% or less, more preferably 70 weight-% or less, more preferably 65 weight-% or less, more preferably 60 weight-% or less, more preferably 50 weight-% or less, more preferably 40 weight-% or less, more preferably 30 weight-% or less, more preferably 20 weight-% or less, more preferably 10 weight-% or less, of the one or more thermoplastic(s) TP1.42. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe mixture M1 and / or the polymer composition PC1 and / or the product PRF1 exhibit(s) a ratio (weight- % / weight-%) of the one or more thermoplastic(s) TP1 to the composition C1 of 0.1 or more, preferably 0.2 or more, more preferably 0.3 or more, more preferably 0.4 or more, more preferably 0.5 or more, more preferably0.6 or more, more preferably 0.7 or more, more preferably 0.8 or more, more preferably 0.9 or more.43. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe mixture M1 and / or the polymer composition PC1 and / or the product PRF1 exhibit(s) a ratio (weight- 240470 23 % / weight-%) of the one or more thermoplastic(s) TP1 to the composition C1 of 0.9 or less, preferably 0.8 or less, more preferably 0.7 or less, more preferably 0.6 or less, more preferably 0.5 or less, more preferably 0.4 or less, more preferably 0.3 or less, more preferably 0.2 or less, more preferably 0.1 or less.44. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s), preferably consists of, in weight-%: 1 to 98, preferably 20 to 90, more preferably 30 to 80, more preferably 40 to 70 the one or more thermoplastic(s) TP1, 1 to 50, preferably 3 to 40, more preferably 5 to 30, more preferably 10 to 20 the one or more thermoset(s) TS1, 1 to 70, preferably 10 to 60, more preferably 20 to 50, more preferably 20 to 40 the glass fibres GF1, and 0 to 50, preferably 1 to 40, more preferably 5 to 30, more preferably 10 to 20 the one or more additive(s) A1.45. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s), preferably consists of, in weight-%: 1 to 99, preferably 20 to 90, more preferably 30 to 80, more preferably 40 to 70 the one or more thermoplastic(s) TP1, 1 to 80, preferably 15 to 70, more preferably 30 to 60, more preferably 40 to 50 the composition C1, and 0 to 50, preferably 1 to 40, more preferably 5 to 30, more preferably 10 to 20 the one or more additive(s) A1.46. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe polymer composition PC1 and / or the product PRF1 exhibit(s) an E modulus EM RT of 3000 MPa or more, preferably 4000 MPa or more, more preferably 5000 MPa or more, more preferably 6000 MPa or more, more preferably 7000 MPa or more, more preferably 7500 MPa or more, more preferably 8000 MPa or more, more preferably 8500 MPa or more.47. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe polymer composition PC1 and / or the product PRF1 exhibit(s) an E modulus EMRT of 15000 MPa or less, preferably 14000 MPa or less, more preferably 13000 MPa or less, more preferably 12000 MPa or less, more preferably 11000 MPa or less, more preferably 10500 MPa or less, more preferably 10000 MPa or less, more preferably 9500 MPa or less, more preferably 9000 MPa or less.48. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe polymer composition PC1 and / or the product PRF1 exhibit(s) a tensile strength at yield sM RT of 10 MPa or more, preferably 30 MPa or more, more preferably 50 MPa or more, more preferably 70 MPa or more, more preferably 90 MPa or more, more preferably 100 MPa or more, more preferably 110 MPa or more, more pref- erably 120 MPa or more.49. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe polymer composition PC1 and / or the product PRF1 exhibit(s) a tensile strength at yield sM RT of 250 MPa or less, preferably 200 MPa or less, more preferably 175 MPa or less, more preferably 150 MPa or less, more preferably 140 MPa or less, more preferably 130 MPa or less.50. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe polymer composition PC1 and / or the product PRF1 exhibit(s) an elongation at break eB RT of 0.1 % or more, preferably 0.5 % or more, more preferably 1.0 % or more, more preferably 1.5 % or more, more preferably 2.0 % or more, more preferably 2.2 % or more.51. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe polymer composition PC1 and / or the product PRF1 exhibit(s) an elongation at break eBRT of 70 % or less, preferably 60 % or less, more preferably 50 % or less, more preferably 40 % or less, more preferably 30 % or less, more preferably 20 % or less, more preferably 10 % or less, more preferably 5 % or less, more preferably 4 % or less, more preferably 3 % or less, more preferably 2.5 % or less.52. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length d0.10length of 10 µm or more, preferably 25 µm or more, more preferably 50 µm or more, more preferably 75 µm or more, more preferably 100 µm or more; and / or, preferably and, 1000 µm or less, preferably 750 µm or less, more preferably 500 µm or less, more preferably 250 µm or less, more preferably 200 µm or less, more preferably 150 µm or less, more preferably 110 µm or less.53. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length d0.50length of 10 µm or more, preferably 100 µm or more, more preferably 200 µm or more, more preferably 250 µm or more, more preferably 290 µm or more; and / or, preferably and, 1000 µm or less, preferably 750 µm or less, more preferably 600 µm or less, more preferably 500 µm or less, more preferably 400 µm or less, more pref-erably 350 µm or less, more preferably 300 µm or less.54. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length <50µmlengthof 0.5 % or more, preferably 2.0 % or more, more preferably 2.5 % or more, more preferably 3.0 % or more, more preferably 3.4 % or more; and / or, preferably and, 20 % or less, preferably 15 % or less, more preferably 12 % or less, more preferably 10 % or less, more preferably 5.0 % or less, more preferably 4.0 % or less, more preferably 3.6 % or less. 2555. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length <100µmlength of 1 % or more, preferably 5 % or more, more preferably 8 % or more, more preferably 9 % or more, more preferably 9.5 % or more; and / or, preferably and, 50 % or less, preferably 30 % or less, more preferably 20 % or less, more preferably 15 % or less, more preferably 12.0 % or less, more preferably 11.0 % or less, more preferably 10.5 % or less.56. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length <200µmlengthof 1 % or more, preferably 10 % or more, more preferably 18 % or more, more preferably 22 % or more, more preferably 26 % or more; and / or, preferably and, 80 % or less, preferably 60 % or less, more preferably 40 % or less, more preferably 35 % or less, more preferably 32 % or less, more preferably 30 % or less, more pref- erably 28 % or less.57. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length d0.10frequencyof 1 µm or more, preferably 25 µm or more, more preferably 35 µm or more, more preferably 38 µm or more, more preferably 41 µm or more; and / or, preferably and, 80 µm or less, preferably 70 µm or less, more preferably 60 µm or less, more preferably 50 µm or less, more preferably 48 µm or less, more preferably 45 µm or less, more preferably 43 µm or less.58. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length d0.50frequency of 10 µm or more, preferably 100 µm or more, more preferably 125 µm or more, more preferably 150 µm or more, more preferably 155 µm or more; and / or, preferably and, 1000 µm or less, preferably 750 µm or less, more preferably 500 µm or less, more preferably 400 µm or less, more preferably 200 µm or less, more pref- erably 180 µm or less, more preferably 170 µm or less.59. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length <50µmfre-quencyof 0.5 % or more, preferably 5.0 % or more, more preferably 10.0 % or more, more preferably 12.0 % or more, more preferably 16.0 % or more; and / or, preferably and, 80 % or less, preferably 45 % or less, more preferably 40 % or less, more preferably 35 % or less, more preferably 25 % or less, more preferably 20 % or less, more preferably 18 % or less.60. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length <100µmfre- quency of 1 % or more, preferably 15 % or more, more preferably 30 % or more, more preferably 32 % or more, 240470 26 more preferably 35 % or more; and / or, preferably and, 80 % or less, preferably 60 % or less, more preferably 50 % or less, more preferably 45 % or less, more preferably 42 % or less, more preferably 40 % or less, more preferably 37 % or less.61. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe glass fibres GF1 in the polymer composition PC1 and / or the product PRF1 exhibit a fibre length <200µmfre- quency of 5 % or more, preferably 35 % or more, more preferably 50 % or more, more preferably 55 % or more, more preferably 57 % or more; and / or, preferably and, 90 % or less, preferably 80 % or less, more preferably 70 % or less, more preferably 65 % or less, more preferably 61 % or less, more preferably 59 % or less.62. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe one or more thermoset(s) TS1 is / are an unsaturated polyester and / or an epoxy resin, preferably an epoxyresin.63. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe one or more thermoset(s) TS1 is / are obtainable by the reaction of component A comprising one or moremonomer(s) comprising one or more epoxide groups and a component B comprising one or more monomer(s) comprising one or more amine group(s), preferably primary amine group(s).64. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe decomposition temperature of the one or more thermoset(s) TS1 is / are 200 °C or more and 800°C or less,preferably 300 °C or more and 700 °C or less, more preferably, 350 °C or more and 600 °C or less, more preferably, 400 °C or more and 500 °C or less.65. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe mixture M1 and / or the polymer composition PC1 and / or the product PRF1 is / are a dispersion comprising particles PR1 comprising the one or more thermoset(s) TS1, preferably and the glass fibres GF1, more prefer- ably the composition C1, and a phase, preferably a continuous phase, comprising the one or more thermo- plastic(s) TP1.66. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe mixture M1 and / or the polymer composition PC1 and / or the product PRF1 comprise(s) particles PR1 com- prising, preferably consisting of, the one or more thermoset(s) TS1, preferably and the glass fibres GF1, more preferably the composition C1.67. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe particle(s) PR1 and / or the glass fibres GF1 and / or the composition C1 are at least partially wrapped by the one or more thermoplastic(s) TP1. 240470 2768. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe polymer composition PC1 comprises glass fibre GF1 which are at least partially wrapped by the one or more thermoset(s) TS1.69. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe mixture M1 and / or the polymer composition PC1 and / or the product PRF1 is not homogeneous.70. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 is a free flowing composition.71. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 comprises a bulk density [g / cm3] of 1.0 or more, preferably 1.5 or more, preferably 2.0 or more.72. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 comprises a bulk density [g / cm3] of 0.9 or more, preferably 1.1 or more, preferably 1.3 or more, preferably 1.5 or more.73. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe glass fibres GF1 are long glass fibres, preferably continuous glass fibres.74. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe component C1 comprises, preferably consists of, continuous glass fibres GF1, and wherein the continuous glass fibres GF1 are assembled to form a unidirectional and multidirectional glass fibres textile.75. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe component C1 comprises, preferably consists of, continuous glass fibres GF1, and wherein the continuous glass fibres GF1 are arranged in one or more textile plie(s), and wherein one or more textile plie(s) of the continuous glass fibres GF1 are assembled to reach a multitude of orientations, preferably wherein the one or more textile plies(s) are two or more textile plies(s), more preferably 2 to 200 textile plies(s), more preferably 3 to 50 textile plies(s).76. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe glass fibres GF1 in the polymer composition PC1 are isotropically distributed.77. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe glass fibres GF1 form a textile T1 and wherein the textile T1 is a nonwoven textile. 240470 2878. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe glass fibres GF1 in the composition C1 are not woven, knitted, braided, or laid.79. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe one or more thermoplastic(s) TP1 is / are selected from polyamide, polypropylene, polyethylene, polyester,styrene, polyvinylchloride PVC, polyoxymethylene POM, polyketone, polyether ether ketone PEEK, polyimide and mixtures thereof, preferably is a polyamide.80. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe polyamide is selected from PA6, PA 66, PA56, PA 610, PA11, PA12, PA1010, PA1012, PPA, PA46; and mixtures and / or copolymers thereof, preferably PA 6, PA 66; and mixtures and / or copolymers thereof; and mix- tures thereof, more preferably is PA 6.81. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe method is a method for the production of a polymer composition and / or a polymer product, preferably wherein the polymer composition and / or polymer product exhibit(s) an increased recycling content of the glassfibres, an increased recycling content of the thermoset, improved mechanical properties, and / or, preferably and, a decreased product carbon footprint.82. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe product PRF1 is not (a) wind rotor blade(s) and / or wind turbine blade(s).83. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe product PRF1’ is not (a) wind rotor blade(s) and / or wind turbine blade(s).84. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 is not derived from (a) wind rotor blade(s) and / or wind turbine blade(s).85. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe one or more thermoplastic(s) TP1 is / are not a foam.86. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe one or more thermoplastic(s) TP1 and / or polymer composition PC1 and / or polymer product PRF1 exhibit(s) a density of 0.4 g / cm3or more, preferably 0.6 g / cm3or more, more preferably 0.8 g / cm3or more, more preferably 1.0 g / cm3or more, more preferably 1.2 g / cm3or more. 240470 2987. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe one or more thermoplastic(s) TP1 and / or polymer composition PC1 and / or polymer product PRF1 exhibit(s) adensity of 2.0 g / cm3 or less, preferably 1.6 g / cm3 or less, more preferably 1.4 g / cm3 or less.88. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 exhibits a sandwich structure, preferably in which glass fibres GF1 form the core and theone or more thermoset(s) TS1, preferably and the one or more additive(s) A1, form(s) the skins.89. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, wherein, inthe composition C1, the glass fibres GF1 are held in the one or more thermoset(s) TS1, preferably and the oneor more additive(s) A1, by mechanical anchoring and / or chemical adhesion, preferably by a combination of mechanical anchoring and chemical adhesion.90. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 exhibits a layered structure.91. Method, polymer composition PC1 and / or use according to any one of the preceding embodiments, whereinthe composition C1 exhibits a layered structure, in which glass the glass fibres GF1 are present as fabric plies,two or more of the fabric plies are laid up together and the one of more thermoset(s) TS1, preferably and the one or more additive(s) A1, are interpenetrated in the fabric plies and between the fabric plies.Examples The invention is further illustrated by the following examples:(A1) Polyamide 6 (PA6) (Ultramid® B27E; BASF SE)(B1) Composition C1 (obtained from shredded wind rotor blade (glass fibre content 68 weight-%)The compounds given in Table 1 were compounded with a Xplore micro-compounder twin-screw extruder (at 80 rpmwith a housing temperature of 260°C and a residence time of 3 min). After compounding, test specimens were formedusing a Xplore injection moulding machine and then measured. The results are also summarized in Table 1. 240470 30Table 1: Contents and results of examples 1 and 2Example 1 Example 2Compound A1 weight-% 100 56Compound B1 weight-% - 44E modulus EM RT MPa 2980 8960Tensile strength at yield sM RT MPa 63 124Elongation at break eB RT % 71 2.2Fibre content in polymer composition PC1 weight-% - 32.3Fibre length d0.10length µm - 106Fibre length d0.50length µm - 296Fibre length <50µmlength % - 3.5Fibre length <100µmlength % - 10Fibre length <200µmlength % - 27Fibre length d0.10frequency µm - 42Fibre length d0.50frequency µm - 159Fibre length <50µmfrequency % - 17Fibre length <100µmfrequency % - 36Fibre length <200µmfrequency % - 58

Claims

1. 240470 31 Claims1. Method comprising the steps:- providing:- one or more thermoplastic(s) TP1, and- a composition C1 comprising:- one or more thermoset(s) TS1,- glass fibres GF1, and- preferably one or more additive(s) A1;- preferably comminuting the composition C1; and- mixing and heating a mixture M1 comprising:- the one or more thermoplastic(s) TP1,- the composition C1, and- preferably one or more additive(s) A1,to obtain a polymer composition PC1.

2. Method according to claim 1, wherein, in the heating step, the mixture M1 is heated to a temperature of 150 °Cor more, preferably 200 °C or more, more preferably 210 °C or more, more preferably 220 °C or more, more preferably 230 °C or more, more preferably 240 °C or more, more preferably 250 °C or more; and / or 400 °C or less, preferably 320 °C or less, more preferably 300 °C or less, more preferably 290 °C or less, more preferably 280 °C or less, more preferably 270 °C or less, more preferably 260 °C or less.

3. Method according to claim 1 or 2, wherein, in the heating step, the mixture M1 is heated for 30 seconds or more,preferably 1 minute or more; and / or 5 hours or less, preferably 4 hours or less, more preferably 3 hours or less, more preferably 2 hours or less, more preferably 1 hours or less, more preferably 50 minutes or less, more preferably 30 minutes or less, more preferably 10 minutes or less, more preferably 5 minutes or less.

4. Method according to any one of the preceding claims, wherein the composition C1 is obtainable by vacuuminfusion or pultrusion or resin transfer moulding or filament winding, preferably vacuum infusion, of glass fibres GF0; wherein the fibres GF0 and / or the glass fibres GF1 is / are continuous glass fibres; and / or wherein the composition C1 comprises glass fibres GF1 exhibiting a length of the average grain size of thecomposition C1, preferably after comminuting.

5. Method according to any one of the preceding claims, wherein the composition C1 exhibits an average grainsize of 0.1 mm or more, preferably 0.2 mm or more, more preferably 0.3 mm or more, more preferably 0.4 mm or more, more preferably 0.5 mm or more, more preferably 0.7 mm or more, more preferably 1.0 mm or more; and / or 500.0 mm or less, preferably 400.0 mm or less, more preferably 300.0 mm or less, more preferably 200.0240470 32 mm or less, more preferably 100.0 mm or less, more preferably 50.0 mm or less, more preferably 25.0 mm or less, more preferably 20.0 mm or less, more preferably 15.0 mm or less, more preferably 10.0 mm or less, more preferably 5.0 mm or less.

6. Method according to any one of the preceding claims, wherein the composition C1 is or is derived from wasteW1, preferably wherein the waste W1 comprises, preferably consists of, wind rotor blade(s), tube(s), construc-tion element(s), part(s) of a means of transport; preferably bike, car and / or ship; more preferably wind rotorblade(s).

7. Method according to any one of the preceding claims, wherein the mixture M1 and / or the polymer compositionPC1 comprise(s), preferably consist(s) of, in weight-%:1 to 99, preferably 20 to 90, more preferably 30 to 80, more preferably 40 to 70 the one or more thermoplastic(s) TP1, 1 to 80, preferably 15 to 70, more preferably 30 to 60, more preferably 40 to 50 the composition C1, and 0 to 50, preferably 1 to 40, more preferably 5 to 30, more preferably 10 to 20 the one or more additive(s) A1.

8. Method according to any one of the preceding claims,wherein the one or more thermoset(s) TS1 is / are an unsaturated polyester and / or an epoxy resin, preferably anepoxy resin; and / or wherein the one or more thermoplastic(s) TP1 is / are selected from polyamide, polypropylene, polyethylene,polyester, styrene, polyvinylchloride PVC, polyoxymethylene POM, polyketone, polyether ether ketone PEEK, polyimide and mixtures thereof, preferably is a polyamide.

9. Method according to any one of the preceding claims, wherein the mixture M1 and / or the polymer compositionPC1 is / are a dispersion comprising particles PR1 comprising the one or more thermoset(s) TS1, preferably and the glass fibres GF1, more preferably the composition C1, and a phase, preferably a continuous phase, com- prising the one or more thermoplastic(s) TP1.

10. Method according to any one of the preceding claims, wherein the method comprises the step(s):- converting the polymer composition PC1 to obtain a product PRF1, and / or- recycling the product PRF1 to obtain a product PRF1’.

11. Method according to any one of the preceding claims, wherein the product PRF1 and / or product PRF1’ is / areselected from: i) building block or monomer; orii) polymer, preferably polymer A, polymer composition, preferably polymer composition A, or polymer prod-uct, preferably polymer product A; or240470 33 iii) cleaning polymer, cleaning surfactant, descaling compound, cleaning biocide or composition or formu-lation thereof; or iv) agrochemical composition, agrochemical formulation auxiliary or agrochemically active ingredient; orv) active pharmaceutical ingredient or intermediate thereof, pharmaceutical excipient, animal feed additive,human food additive, dietary supplements, aroma chemical or aroma composition; or vi) aqueous polymer dispersion, preferably polyurethane or polyurethane – poly(meth)acrylate hybrid poly-mer dispersion, emulsion, binder for paper and fibre coatings, UV-curable acrylic polymer for hot melts and coatings polyisocyanates, hyperbranched polyester polyol, polymeric dispersant for inorganic binder compositions, unsaturated polyester polyol or 100% curable composition; or vii) cosmetic surfactant, emollient, wax, cosmetic polymer, UV filter, further cosmetic ingredient or composi-tion or formulation thereof; or viii) polymer B, polymer composition B, coating composition, other functional composition, foil, molded body,coating or coated substrate.

12. Method according to any one of the preceding claims, wherein the content of the composition C1 in the polymercomposition PC1 and / or product PRF1 and / or product PRF1’ is 1 weight-% or more, preferably 2 weight-% or more, more preferably 5 weight-% or more, more preferably 15 weight-% or more, more preferably 30 weight- % or more, more preferably 40 weight-% or more, more preferably 60 weight-% or more, more preferably 80 weight-% or more, more preferably 90 weight-% or more, more preferably 95 weight-% or more; and / or wherein the content of the composition C1 in the polymer composition PC1 and / or product PRF1 and / or product PRF1’ is 99 weight-% or less, preferably 95 weight-% or less, more preferably 90 weight-% or less, more pref-erably 50 weight-% or less, more preferably 25 weight-% or less, more preferably 10 weight-% or less; and preferably wherein the content is determined based on identity preservation and / or segregation and / or mass balance and / or book and claim chain of custody models, preferably based on mass balance, preferably the International Sustainability and Carbon Certification (ISCC) standard.

13. Method according to any one of the preceding claims, wherein the method is a method for the production of apolymer composition and / or a polymer product, preferably wherein the polymer composition and / or polymer product exhibit(s) an increased recycling content of the glass fibres, an increased recycling content of the ther-moset, improved mechanical properties, and / or, preferably and, a decreased product carbon footprint.

14. Polymer composition PC1 or product PRF1, preferably obtainable by or obtained by a method according to anyone of the preceding claims, comprising, preferably consisting of: -one or more thermoplastic(s) TP1,- a composition C1, and- preferably one or more additive(s) A1;wherein the composition C1 comprises, preferably consists of, -one or more thermoset(s) TS1,240470 34 -glass fibres GF1, and- preferably one or more additive(s) A1.

15. Use of a composition C1 comprising:- one or more thermoset(s) TS1,- glass fibres GF1, and- preferably one or more additive(s) A1;as a component and / or as an additive, preferably as a reinforcing agent, in a polymer composition PC1 com-prising one or more thermoplastic(s) TP1 and / or in a product PRF1 comprising one or more thermoplastic(s) TP1.

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