EP2927910A1 - Medium- or high-voltage electrical device - Google Patents

Abstract

The present invention relates to an electrical device (1,20,30) comprising a crosslinked layer (3,4,5,21,22,23,31,32) for surrounding or surrounding an elongate electrically conductive element, characterized in that the crosslinked layer is obtained from a polymer composition comprising: at least one olefin polymer (A), and a crosslinking agent (B) comprising one or more oxazoline functions, the polymer A comprising one or more reactive functional groups capable of reacting with the oxazoline function of the crosslinking agent B.

Description

The present invention relates to an electric device of the electric cable type or accessory for electric cable. It applies typically, but not exclusively, to the fields of low-voltage (in particular less than 6kV), medium-voltage (in particular 6 to 45-60 kV) or high-voltage (especially greater than 60 kV) energy cables. , and up to 800 kV), whether DC or AC.

The energy cables typically comprise a central electrical conductor and at least one electrically insulating layer crosslinked by techniques well known to those skilled in the art, especially peroxide.

The peroxide route tends to be more and more avoided with respect to peroxide decomposition products, presenting disadvantages during the manufacture of the cable, or even once the cable in operational configuration. Indeed, during the crosslinking, the peroxides decompose and form crosslinking by-products such as in particular methane, acetophenone, cumyl alcohol, acetone, tert-butanol, alpha-2 methyl styrene and / or water. The formation of water from cumyl alcohol is relatively slow and can occur after several months or even years once the cable is in operational configuration. The risk of breakdown of the crosslinked layers is thus significantly increased. In addition, if the methane formed during the crosslinking step is not removed from the crosslinked layers, risks related to the explosiveness of methane and its ability to ignite should not be ignored. This gas can also cause damage once the cable is put into service. Even if solutions exist to limit the presence of methane within the cable, such as for example to treat the cable thermally to accelerate the diffusion of methane outside the cable, they become long and expensive when the thickness of the crosslinked layers is important.

By way of example of a crosslinking process which does not use the peroxide route, mention may be made of the document U.S. 4,826,726 who describes a cable heat resistant electrical apparatus comprising an elongated electrical conductor surrounded by a crosslinked layer obtained from a composition comprising an ethylene copolymer comprising an oxirane function, and a polymeric compound as a crosslinking agent, of the ethylene copolymer type and unsaturated dicarboxylic acid anhydride.

However, once said crosslinked composition, the layer obtained does not have optimum properties of tensile strength and elongation at break, especially during the life of the electric cable (see aging).

The object of the present invention is to overcome the drawbacks of the prior art techniques by providing an electrical device, in particular of the electric cable or accessory type for electric cable, comprising a crosslinked layer whose manufacture significantly limits the presence of sub cross-linking products, such as for example methane and / or water, while guaranteeing optimum mechanical properties (tensile strength and elongation at break) during the lifetime of said electrical device.

• au moins un polymère d'oléfine (A), et
• un agent de réticulation (B) comprenant une ou plusieurs fonctions oxazoline,

le polymère d'oléfine (A) comprenant une ou plusieurs fonctions réactives apte(s) à réagir avec la fonction oxazoline de l'agent de réticulation (B).The subject of the present invention is an electrical device, in particular of the electric cable or accessory type for an electric cable, comprising a crosslinked layer capable of surrounding or surrounding an elongated electrically conductive element, characterized in that the crosslinked layer is obtained from a polymeric composition comprising:

• at least one olefin polymer (A), and
• a crosslinking agent (B) comprising one or more oxazoline functions,

the olefin polymer (A) comprising one or more reactive functional groups capable of reacting with the oxazoline function of the crosslinking agent (B).

Thanks to the invention, the crosslinked layer makes it possible to avoid the use of organic peroxide, while at the same time guaranteeing a high level of crosslinking, and secondly very good mechanical properties such as tensile strength and elongation at break according to standard NF EN 60811-1-1, during the life of the electrical device.

In addition, the crosslinked layer of the invention has the advantage of being economical, easy to implement, in particular by extrusion, and easy to manufacture, since it does not require the use of binding degassing processes.

Olefin polymer (A)

The olefin polymer of the invention comprises one or more reactive functional groups capable of reacting with the oxazoline function of the crosslinking agent B, to allow the polymer A to crosslink.

Said reactive function will react directly on the oxazoline function after opening the oxazoline during a rise in temperature.

The reactive function of the polymer A may be chosen from a carboxyl function, a precursor of the carboxyl function, for example an anhydride, an aromatic thiol function, and a phenol function.

Thus, the chemical reaction between the reactive function of the polymer A of the carboxylic functional group and of the oxazoline function of the crosslinking agent B will make it possible to form a stable amide function, covalently bound to an ester function: the ester function originating from the reactive function of the polymer A and the amide function originating from the oxazoline of the crosslinking agent B. This chemical crosslinking reaction can be illustrated as follows, under the action of heat (Δ):

A ₁ symbolizes the structure of the polymer A, and B ₁ symbolizes the structure of the crosslinking agent B.

During this crosslinking reaction, no toxic product is formed.

The polymer A of the invention may comprise at most 20% by weight of reactive function, and preferably at most 10% by weight of reactive function, relative to the total weight of polymer A.

The polymer A of the invention may comprise at least 0.2% by weight of reactive functional group, and preferably at least 1% by weight of reactive function, relative to the total weight of polymer A.

Of course, mixtures of different polymers A may be envisaged in the context of the invention, in particular with different amounts of reactive function.

The olefin polymer A (ie olefin polymer comprising one or more reactive functional groups capable of reacting with the oxazoline function of the crosslinking agent B) is obtained from the polymerization of at least one monomer d olefin, said olefin monomer being preferably an ethylene monomer. In this respect, the olefin polymer A is preferably an ethylene polymer comprising one or more reactive functional groups capable of reacting with the oxazoline function of the crosslinking agent B.

The olefin polymer A may be of the thermoplastic or elastomeric type.

Preferably, the olefin A polymer is of the thermoplastic type, in order to optimize the desired properties, in particular the electrical properties. Thermoplastic polymers conventionally have a readily determinable melting point by Differential Scanning Calorimetry (DSC) according to ASTM D 3418.

The olefin A polymer may have a melt flow index (MFI), known in English under the acronym MFI for "Melt Flow Index" or under the acronym MFR for "Melt Flow Rate", between 0.25 and 20 (limits included), preferably between 0.5 and 15 (inclusive), and even more preferably between 5 and 12 (inclusive), expressed in grams / 10 minutes, according to ASTM D 1238 at 190 ° C / 2 , 16 kg.

The temperature (ie 190 ° C.) and the weight (ie 2.16 kg) mentioned in accordance with ASTM D 1238 respectively refer to the temperature of the sleeve and the die of the measuring apparatus, and to the total mass of the piston with load that presses the material to be measured to push it through the die of said apparatus.

The term "polymer" is understood to mean any type of polymer well known to those skilled in the art, such as, for example, homopolymer, copolymer, terpolymer, block copolymer, etc.

The olefin A polymer may be based on a homopolymer of ethylene or of an ethylene copolymer chosen from high density polyethylenes (HDPE), medium density polyethylenes (MDPE) and low density polyethylenes (LDPE). ), linear low density polyethylenes (LLDPE), and very low density polyethylenes (VLDPE).

According to a first variant, the reactive function of the polymer A can be grafted onto said polymer, or more particularly on the macromolecular chain of the polymer A, which is of the olefin polymer type.

According to this first variant, the polymer A of the invention is a so-called "grafted" polymer. Thus, the polymer A may be an olefin polymer comprising said reactive functions grafted onto the polymer. In other words, the polymer according to the invention may be a polymer comprising at least one reactive function grafted on the macromolecular chain (ie main chain or " backbone ") of said polymer. The ends of the macromolecular chain of the polymer may in turn be grafted or not with said reactive function.

By way of example, mention may be made, as polymer A of the first variant, of grafted polyethylene maleic anhydride.

According to a second variant, the polymer A of the invention may be an olefin copolymer and a monomer bearing the reactive function. In other words, the polymer A may be a copolymer obtained from the polymerization of at least two monomers, one being an olefin and the other being a monomer comprising said reactive function. Said monomer comprising said reactive functional group may be chosen from unsaturated carboxylic acid monomers, comprising in particular a carbon-carbon double bond, such as, for example, the monomers of acrylic acid, methacrylic acid, maleic acid, fumaric acid, crotonic acid, isocrotonic acid, tiglic acid, vinyl acetic acid, 2-pentenoic acid, 3-pentenoic acid, allyl acetic acid, angelic acid, citraconic acid, or mesaconic acid.

By way of example, mention may be made of copolymers of ethylene and of methacrylic acid, or copolymers of ethylene and of acrylic acid.

Terpolymers, or in other words copolymers obtained from three monomers, may also be considered within the scope of the invention. In this case, the polymer A may be a copolymer obtained from the polymerization of three different monomers, the first being an olefin, and the second and third being monomers comprising said reactive function. Said monomers comprising said reactive functional group may be chosen independently from unsaturated carboxylic acid monomers and their derivatives, comprising in particular a carbon-carbon double bond, such as, for example, the monomers of acrylic acid, methacrylic acid, of acid maleic acid, fumaric acid, crotonic acid, isocrotonic acid, tiglic acid, vinyl acetic acid, 2-pentenoic acid, 3-pentenoic acid, allyl acetic acid, angelic acid, citraconic acid, or mesaconic acid.

By way of example, mention may be made of terpolymers of ethylene, methacrylic acid and acrylic acid.

The melting temperature of the polymers A of the present invention may be from 80 to 170 ° C, preferably from 80 to 120 ° C, and preferably from 90 to 115 ° C. The melting temperature of a polymer is conventionally measured at the melting peak of said polymer by differential scanning calorimetry (DSC) with a temperature ramp of 20 ° C./min under a nitrogen atmosphere.

The polymer A of the invention is a polymer that can be shaped by extrusion.

The polymer A of the invention may be of the olefin homopolymer or copolymer type. Preferably, said olefin polymer is a noncyclic olefin polymer.

In the present invention, it will be preferred to use an ethylene polymer (homo- or copolymer of ethylene) or a propylene polymer (homo- or copolymer of propylene).

According to the first variant of the invention, described above, it is possible to use an olefin homopolymer grafted reactive function, or an olefin copolymer grafted reactive function, the reactive function may be preferably a carboxyl function.

According to the second variant of the invention, described above, it is possible to use a copolymer obtained from an olefin monomer and a monomer comprising at least one reactive function.

The polymer composition of the invention may comprise more than 50.0 parts by weight of polymer A per 100 parts by weight of polymer (s) (i.e., polymeric matrix) in the polymer composition; preferably at least 70 parts by weight of polymer A per 100 parts by weight of polymer (s) in said polymer composition; preferably at least 90 parts by weight of polymer A per 100 parts by weight of polymer (s) in said polymer composition, and particularly preferably only one or more polymers A.

In the present invention, the olefin polymer A is preferably not a polyacrylate. More particularly, polymer A does not comprise an ester function of general formula RCOOR '. Indeed, the ester functions are not at all advantageous for the mechanical properties sought in the field of cabling of the invention.

Polyacrylates are typically obtained by the polymerization of acrylic ester (s), especially without the presence of olefin monomer.

In the case where the polyacrylate is obtained without the presence of olefin monomer, the olefin polymer A is very different from the polyacrylate, since the olefin polymer A is obtained by the polymerization from at least one monomer of olefin.

As examples of polyacrylates, mention may be made of alkyl acrylate copolymers.

Polyacrylates therefore all have pendant ester functions on their macromolecular chain, these functions preferably not falling within the scope of the invention.

Indeed, the polyacrylates described above are not at all advantageous for the mechanical properties sought in the field of cabling of the invention.

In a particular embodiment, the polymer composition may comprise less than 10 parts by weight of polyacrylate, and preferably less than 5 parts by weight of polyacrylate, per 100 parts by weight of polymer (s) in the composition. Preferably, the polymeric composition does not include a polyacrylate. More particularly, the device of the invention does not comprise a polyacrylate.

In the present invention, the olefin polymer A is preferably not a polyimide. More particularly, the polymer A does not comprise an imide functional group of general formula (RCO) ₂ NR '. Indeed, the imide functions are not at all advantageous for the mechanical properties sought in the field of cabling of the invention.

In a particular embodiment, the polymer composition may comprise less than 10 parts by weight of polyimide, and preferably less than 5 parts by weight of polyimide, per 100 parts by weight of polymer (s) in the composition. Preferably, the polymeric composition does not comprise polyimide. More particularly, the device of the invention does not comprise polyimide.

On the other hand, the polymer composition may comprise less than 10 parts by weight of fluoropolymer, and preferably less than 5 parts by weight of fluoropolymer, per 100 parts by weight of polymer (s) in the composition. Preferably, the polymer composition does not include a fluoropolymer. More particularly, the device of the invention does not comprise a fluoropolymer.

In the present invention, when we speak of "100 parts by weight of polymer (s)", it is preferentially understood to mean the polymer or polymers different from the crosslinking agent B in the polymer composition (when the crosslinking agent B is in the form of polymer).

Particularly advantageously, the constituent polymer (s) of the polymer composition (ie the polymer matrix) are solely one or more olefin-based polymers.

The polymer composition of the invention may comprise at least 40.0% by weight of polymer (s), and preferably at least 50.0% by weight of polymer (s), relative to the total weight of the polymer composition, thus forming the polymer matrix of the invention. Preferably, the polymer composition of the invention may comprise at most 99.8% by weight of polymer (s), and preferably at most 96.0% by weight of polymer (s), relative to the total weight of the polymer. polymeric composition.

In the present invention, the polymer matrix does not include in particular the crosslinking agent B when it is in the form of a polymer.

Crosslinking agent (B)

The crosslinking agent B of the invention comprises at least two reactive functions intended to react with the reactive function (s) of the olefin polymer A. At least one of these two reactive functions is an oxazoline function. Preferably, the crosslinking agent B can comprise at least two oxazoline functions.

The crosslinking agent B of the invention may be a polymeric compound or a non-polymeric compound. Preferably, the crosslinking agent is different from the polymer A.

The oxazoline function is a function whose general formula (I) is as follows:

B ₁ symbolizes the structure of the crosslinking agent B which carries at least one of this oxazoline function.

B ₁ can therefore be the macromolecular chain of a polymer or a non-polymeric compound of the aliphatic or aromatic type.

The oxazoline function can be covalently attached to B ₁ by a carbon unit, an ether unit, an ester unit, a urethane unit, a nitrogen, phosphorus or sulfur type heteroatom.

R1, R2, R3 and R4 may be independently selected from hydrogen and alkyl. Preferably, R1, R2, R3 and R4 are hydrogens.

When the crosslinking agent of the invention is of the "non-polymeric" type, it does not result from the covalent linking of a large number of identical or different monomer units, and preferably it does not result from covalent linking of at least two identical or different monomer units.

In a first embodiment in which the crosslinking agent is a polymeric compound, the crosslinking agent is a copolymer functionalized with oxazoline functions. By way of example, mention may be made of the copolymer marketed by Nippon Sokubai under the reference Epocros.

In a second embodiment in which the crosslinking agent is a nonpolymeric compound, the crosslinking agent comprises at least two oxazoline functions.

Non-polymeric compound comprising two oxazoline functions, bis-oxazoline, such as for example 2,2 '- (1,3-phenylene) bis (2-oxazoline) (1,3-PBO), 2 , 2 '- (1,4-phenylene) bis (2-oxazoline) (1,4-PBO) or 2,2' - (2,6-pyridylene) bis (2-oxazoline) (pybox).

When the non-polymeric crosslinking agent comprises more than two oxazoline functions, there may be mentioned, for example, compounds comprising three oxazoline functions, such as 2,2 ', 2 "- (1,3,5-phenylene) -tris- 2-oxazoline or 2,2 ', 2 "- (1,2,4-phenylene) -tris-5-methyl-2-oxazoline.

The oxazoline function of the crosslinking agent (B) is able to react with the reactive function of the polymer to allow crosslinking of the olefin polymer (A).

The crosslinking agent is preferably in powder form in order to facilitate its dosing during its extrusion processing.

Conventionally, the crosslinking kinetics relative to the crosslinking agent, and more particularly the opening of the oxazoline ring, is a function of the temperature of the reaction medium. For example, the crosslinking can be carried out at temperatures of at least 70 ° C, preferably between 70 and 120 ° C, and preferably between 80 and 100 ° C, these temperatures being particularly well adapted for the implementation of the polymer composition of the invention by extrusion.

A temperature below 70 ° C can be used, but the crosslinking will be relatively slow.

A temperature above 200 ° C. at a pressure greater than atmospheric pressure, for a few minutes, may also be used for the crosslinking of the polymer composition of the invention, for example a temperature of between 250 and 350 ° C. , especially at a pressure of 10 bar. These conditions are those typical of crosslinking conditions using a continuous line of vulcanization ("CV line"), in particular a steam or nitrogen line, for the production of cable.

Preferably, the crosslinking agent B has a melting point higher than the melting temperature of the polymer A. The melting temperature of the crosslinking agent B is conventionally measured at the melting peak of said crosslinking agent by differential scanning calorimetry analysis. (DSC) with a temperature ramp of 10 ° C / min under a nitrogen atmosphere.

• du 2,2'-(1,3-phenylene)bis(2-oxazoline) (1,3-PBO) est d'environ 148°C ;
• du 2,2'-(1,4-phenylene)bis(2-oxazoline)(1,4-PBO) est d'environ 242°C ; et
• du 2,2'-(2,6-pyridylene)bis(2-oxazoline) (pybox) est d'environ 157°C.

For example, the melting temperature:

• 2,2 '- (1,3-phenylene) bis (2-oxazoline) (1,3-PBO) is about 148 ° C;
• 2,2 '- (1,4-phenylene) bis (2-oxazoline) (1,4-PBO) is about 242 ° C; and
• 2,2 '- (2,6-pyridylene) bis (2-oxazoline) (pybox) is about 157 ° C.

The polymer composition according to the invention may comprise a sufficient amount of crosslinking agent B in order to carry out the crosslinking of the polymer A.

The polymer composition according to the invention may comprise at most 20.0 parts by weight of crosslinking agent B per 100 parts by weight of polymer (s) in the composition, and preferably at most 15.0 parts by weight of crosslinking agent B per 100 parts by weight of polymer (s) in the composition.

The polymer composition according to the invention may comprise at least 0.1 parts by weight of crosslinking agent B per 100 parts by weight of polymer (s) in the composition, and preferably at least 5 parts by weight of agent crosslinking B per 100 parts by weight of polymer (s) in the composition.

In the present invention, when we speak of "100 parts by weight of polymer (s)", it is preferentially to mean the polymer or polymers different from the crosslinking agent B (when the crosslinking agent B is in the form of polymer).

The polymer composition of the invention may comprise at most 20% by weight of crosslinking agent B, relative to the total weight of the polymer composition.

The polymer composition of the invention may comprise at least 0.1% by weight of crosslinking agent B, relative to the total weight of the polymer composition.

Polymer composition charged

The polymer composition of the invention may further comprise one or more fillers.

The filler of the invention may be a mineral or organic filler. It can be chosen from a flame retardant filler and an inert filler (or non-combustible filler).

By way of example, the flame-retardant filler may be a hydrated filler, chosen in particular from metal hydroxides such as, for example, magnesium dihydroxide (MDH) or aluminum trihydroxide (ATH). These fire-retardant fillers mainly act physically by decomposing endothermically (eg water release), which has the effect of lowering the temperature of the crosslinked layer and to limit the propagation of flames along the electrical device. In particular, we speak of flame retardancy properties, well known under the Anglicism " flame retardant".

The inert filler can be, for its part, chalk, talc, clay (e.g., kaolin), carbon black, or carbon nanotubes.

The charge may also be an electrically conductive charge chosen in particular from carbonaceous charges. By way of example, there can be mentioned as electrically conductive filler carbon blacks, graphenes, carbon nanotubes.

According to a first variant, the electrically conductive filler may be preferred to obtain a crosslinked layer called "semiconductor", and may be introduced into the polymer composition in an amount sufficient to make the semiconductor composition, this amount varying according to the type electrically conductive charge selected. By way of example, the appropriate amount of electrically conductive filler may be from 8 to 40% by weight in the polymer composition for carbon black; and may be from 0.1 to 5% by weight in the polymer composition for carbon nanotubes.

According to a second variant, the electrically conductive filler may be preferred to obtain a so-called "electrically insulating" crosslinked layer, and may be used in small quantities to improve the dielectric properties of an electrically insulating layer, without it becoming semi-transparent. conductive.

The polymer composition may comprise at least 1% by weight of filler (s), preferably at least 10% by weight of filler (s), and preferably at most 50% by weight of filler (s), relative to the weight total of the polymer composition.

According to another characteristic of the invention, and in order to guarantee an electrical device known as HFFR for the Anglicism " Halogen-Free Flame Retardant ", the electrical device, or in other words the elements that make up said electrical device, does not include / preferably include no halogenated compounds. More generally speaking, a so-called halogen-free or "halogen-free" device. These halogenated compounds may be of any kind, such as, for example, fluorinated polymers or chlorinated polymers such as polyvinyl chloride (PVC), halogenated plasticizers, halogenated mineral fillers, etc.

additives

The composition may typically additionally comprise additives in an amount of 0.1 to 20% by weight in the polymer composition.

• des agents de protection, tels que des antioxydants, des anti-UV, des anti-cuivre, des agents anti-arborescences d'eau,
• des agents de mise en oeuvre, tels que des plastifiants, des lubrifiants, des huiles,
• des agents compatibilisants,
• des agents de couplage,
• des retardateurs de grillage,
• des pigments
• des catalyseurs de réticulation,
• des agents modifiant la vitesse de réticulation ;
• et un de leurs mélanges.

The additives are well known to those skilled in the art and can be chosen for example from:

• protective agents, such as antioxidants, anti-UV, anti-copper, anti-tree water agents,
• processing agents, such as plasticizers, lubricants, oils,
• compatibilizing agents,
• coupling agents,
• roasting retardants,
• pigments
• crosslinking catalysts,
• agents that modify the rate of crosslinking;
• and one of their mixtures.

More particularly, the antioxidants make it possible to protect the composition of the thermal stresses generated during the steps of manufacturing the device or operating the device.

• les antioxydants phénoliques à encombrement stérique tels que le tetrakisméthylene(3,5-di-t-butyl-4-hydroxy-hydrocinnamate) méthane, le octadecyl 3-(3,5-di-t-butyl-4-hydroxyphényle)propionate, le 2,2'-thiodiéthylène bis[3-(3,5-di-t-butyl-4-hydroxyphényle) propionate], le 2,2'-Thiobis(6-t-butyle-4-méthylephénol), le 2,2'-méthylenebis(6-t-butyle-4-méthylphénol), le 1,2-Bis(3,5-di-t-butyle-4-hydroxyhydrocinnamoyl) hydrazine, et le 2,2'-oxamido-bis[éthyl 3(3,5-di-t-butyle-4-hydroxyphényle) propionate] ;
• les thioéthers tels que le 4,6-bis(octylthiométhyle)-o-crésol, le bis[2-méthyle-4-{ 3-n-alkyle (C12 ou C14)thiopropionyloxy}-5-t-butylphényle]sulfide et le thiobis-[2-t-butyl-5-méthyle-4,1-phénylène] bis [3-(dodecyltio)propionate] ;
• les antioxydants à base de soufre tels que le Dioctadecyl-3,3'-thiodipropionate ou le Didodecyl-3,3'-thiodipropionate ;
• les antioxydants à base de phosphore tels que les phosphites ou phosphonates comme par exemple le Tris(2,4-di-t-butyl-phényle)phosphite ou le Bis(2,4-di-t-butylphényle) pentaerythritol diphosphite ; et
• les antioxydants de type amine tels que les phénylènes diamines (IPPD, 6PPD...), les diphénylam ines styrènés, les diphénylam ines, les mercapto benzimidazoles et le 2,2,4-trimethyl-1,2 dihydroquinoline polymérisé (TMQ), ce dernier type d'antioxydant étant particulièrement préféré dans la composition de l'invention.

The antioxidants are preferably chosen from:

• hindered phenolic antioxidants such as tetrakismethylene (3,5-di-t-butyl-4-hydroxy-hydrocinnamate) methane, octadecyl 3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate, 2,2'-thiodiethylene bis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate], 2,2'-thiobis (6-t-butyl-4-methylphenol), 2 , 2'-methylenebis (6-t-butyl-4-methylphenol), 1,2-Bis (3,5-di-t-butyl-4-hydroxyhydrocinnamoyl) hydrazine, and 2,2'-oxamido-bis [ethyl 3 (3,5-di-t-butyl-4-hydroxyphenyl) ) propionate];
• thioethers such as 4,6-bis (octylthiomethyl) -o-cresol, bis [2-methyl-4- {3-n-alkyl (C 12 or C 14) thiopropionyloxy} -5-t-butylphenyl] sulfide and the thiobis- [2-t-butyl-5-methyl-4,1-phenylene] bis [3- (dodecyltio) propionate];
• sulfur-based antioxidants such as Dioctadecyl-3,3'-thiodipropionate or Didodecyl-3,3'-thiodipropionate;
• phosphorus-based antioxidants such as phosphites or phosphonates, for example Tris (2,4-di-t-butyl-phenyl) phosphite or bis (2,4-di-t-butylphenyl) pentaerythritol diphosphite; and
• amine antioxidants such as phenylenediamines (IPPD, 6PPD, etc.), diphenylamines styrene, diphenylamines, mercapto benzimidazoles and polymerized 2,2,4-trimethyl-1,2 dihydroquinoline (TMQ), the latter type of antioxidant being particularly preferred in the composition of the invention.

• un grade dit « standard » avec un faible degré de polymérisation, c'est-à-dire avec un taux de monomère résiduel supérieur à 1% en poids et ayant une teneur en NaCl résiduelle pouvant aller de 100 ppm à plus de 800 ppm (parties par million massiques) ;
• un grade dit « à haut degré de polymérisation » avec un haut degré de polymérisation, c'est-à-dire avec un taux de monomère résiduel inférieur à 1% en poids et ayant une teneur en NaCl résiduelle pouvant aller de 100 ppm à plus de 800 ppm ;
• un grade dit « à faible teneur en sel résiduel » avec une teneur en NaCl résiduelle inférieure à 100 ppm.

TMQs can have different grades, namely:

• a so-called "standard" grade with a low degree of polymerization, that is to say with a residual monomer level greater than 1% by weight and having a residual NaCl content ranging from 100 ppm to more than 800 ppm ( parts per million mass);
• a so-called "high degree of polymerization" grade with a high degree of polymerization, that is to say with a residual monomer content of less than 1% by weight and having a residual NaCl content ranging from 100 ppm to more 800 ppm;
• a so-called "low residual salt" grade with a residual NaCl content of less than 100 ppm.

TMQ antioxidants are preferably used when the polymer composition comprises electrically conductive fillers.

The type of stabilizer and its level in the composition of the invention are conventionally chosen as a function of the maximum temperature experienced by the polymers during the production of the mixture and during their preparation. in particular by extrusion, as well as according to the maximum duration of exposure to this temperature.

The crosslinking catalysts are intended to assist in crosslinking. The crosslinking catalyst may be selected from Lewis acids; Brönsted acids; and tin catalysts such as dibutyltin dilaurate (DBTL).

Crosslinking rate modifying agents may react with the oxazoline function to form a modified oxazoline function. They may be polyfunctional molecules comprising at least three functions chosen independently from carboxylic, phenolic and aromatic thiol functions.

The reticulated layer and the electrical device

In the present invention, the crosslinked layer can easily be characterized by determining its gel level according to ASTM D2765-01.

More particularly, said crosslinked layer may advantageously have a gel level, according to ASTM D2765-01 (xylene extraction), of at least 50%, preferably at least 70%, preferably at least 80% by weight. %, and particularly preferably at least 90%.

The crosslinked layer of the invention may be selected from an electrically insulating layer, a semiconductor layer, a stuffing element and a protective sheath. The device of the invention may of course comprise combinations of at least two of these four types of crosslinked layer. The crosslinked layer of the invention may be the outermost layer of the electrical device.

In the present invention, the term "electrically insulating layer" a layer whose electrical conductivity can be at most 1.10 ^-9 S / m (siemens per meter) (at 25 ° C).

When the crosslinked layer of the invention is an electrically insulating layer, the polymer composition of the invention can comprise at least 70% by weight of polymer A, relative to the total weight of the polymer composition, thus forming the polymer matrix of the invention.

In the present invention, the term "semiconductor layer" means a layer whose electrical conductivity can be at least 1.10 ^-9 S / m (siemens per meter), preferably at least 1.10 ^-3 S / m. and preferably may be less than 1.10 ³ S / m (at 25 ° C).

When the crosslinked layer of the invention is a semiconductor layer, the polymer composition of the invention may comprise an electrically conductive filler in an amount sufficient to render the crosslinked layer of the semiconductor invention.

The crosslinked layer of the invention may be an extruded layer or a molded layer, by methods well known to those skilled in the art.

The electrical device of the invention may be an electric cable or an accessory for an electric cable.

According to a first embodiment, the device according to the invention is an electrical cable comprising said crosslinked layer surrounding said elongated electrically conductive element.

When the electrical device is an electrical cable, the crosslinked layer is preferably an extruded layer by techniques well known to those skilled in the art.

The crosslinked layer of the invention can surround the elongated electrically conductive element according to several variants.

According to a first variant, the crosslinked layer may be in direct physical contact with the elongated electrically conductive element. We speak in this first variant of low voltage cable.

• une première couche semi-conductrice entourant l'élément électriquement conducteur,
• une couche électriquement isolante entourant la première couche semi-conductrice, et
• une deuxième couche semi-conductrice entourant la couche électriquement isolante.

According to a second variant, the crosslinked layer may be at least one of the layers of an insulating system comprising:

• a first semiconductor layer surrounding the electrically conductive element,
• an electrically insulating layer surrounding the first semiconductor layer, and
• a second semiconductor layer surrounding the electrically insulating layer.

We speak in this second variant of medium or high voltage cable.

According to a second embodiment, the device according to the invention is an accessory for an electric cable, said accessory comprising said crosslinked layer.

The accessory is intended to surround or surround the elongated electrically conductive element of an electrical cable. More particularly, said accessory is intended to surround or surrounds an electric cable, and preferably it is intended to surround or surround at least one end of an electric cable. The accessory may be in particular a junction or a termination for an electric cable.

The accessory may be typically a hollow longitudinal body, such as for example a junction or termination for electric cable, wherein at least a portion of an electric cable is intended to be positioned.

The accessory comprises at least one semiconductor element and at least one electrically insulating element, these elements being intended to surround one end of an electric cable. The semiconductor element is well known for controlling the geometry of the electric field when the electric cable, associated with said accessory, is energized.

The crosslinked layer of the invention may be said semiconductor element and / or said electrically insulating element of the accessory.

When the accessory is a junction, the latter makes it possible to connect together two electrical cables, the junction being intended to surround or then surrounding at least in part these two electric cables. More particularly, the end of each electrical cable to be connected is positioned inside said junction.

When the device of the invention is a termination for an electric cable, the termination is intended to surround or at least partly surrounds an electric cable. More particularly, the end of the electrical cable to be connected is positioned within said termination.

When the electrical device is an accessory for an electric cable, the crosslinked layer is preferably a layer molded by techniques well known to those skilled in the art.

In the present invention, the elongate electrically conductive element of the electrical cable may be a metal wire or a plurality of twisted or unreinforced metal wires, in particular made of copper and / or aluminum, or one of their alloys.

1. i. extruder la composition polymère autour d'un élément électriquement conducteur allongé, pour obtenir une couche extrudée, et
2. ii. réticuler la couche extrudée de l'étape i.

Another subject of the invention relates to a method of manufacturing an electric cable according to the invention, characterized in that it comprises the following steps:

1. i. extruding the polymer composition around an elongate electrically conductive member to provide an extruded layer, and
2. ii. crosslink the extruded layer of step i.

Step i can be performed by techniques well known to those skilled in the art, using an extruder.

In step i, the extruder output composition is said to be "non-crosslinked", the temperature as well as the processing time within the extruder being optimized accordingly.

By "non-crosslinked" is meant a layer whose gel level according to ASTM D2765-01 (xylene extraction) is at most 20%, preferably at most 10%, preferably at most 5%. %, and particularly preferably 0%.

At the extruder outlet, an extruded layer is thus obtained around said electrically conductive element, which may or may not be directly in physical contact with said electrically conductive element.

Prior to step i, the constituent compounds of the polymer composition of the invention may be mixed, in particular with the polymer A in the molten state, in order to obtain a homogeneous mixture. The temperature within the mixer may be sufficient to obtain a polymer A in the molten state, but is limited to prevent the opening of the oxazoline function of the crosslinking agent B, and therefore the crosslinking of the polymer A. Then, the homogeneous mixture is granulated, by techniques well known to those skilled in the art. These granules can then feed an extruder to perform step i.

During step i of extrusion and / or the preliminary mixing step, the operating temperature within the extruder and / or the mixer may be classically greater than or equal to the melting temperature of the extruder. crosslinking agent B, especially knowing that the melting temperature of the polymer A is preferably lower than the melting temperature of the crosslinking agent B.

As a result, the crosslinking agent B can be mixed particularly homogeneously with the polymer A.

• égale à celle de la température de fusion de l'agent de réticulation B, ou bien
• au plus égale à la température de fusion de l'agent de réticulation B additionnée de 10°C, et de préférence au plus égale à la température de fusion de l'agent de réticulation B additionnée de 5°C,

sachant notamment que la température de fusion du polymère A est de préférence inférieure à la température de fusion de l'agent de réticulation B.In a particularly preferred embodiment, during the extrusion stage i and / or the preliminary mixing step, the operating temperature within the extruder and / or the mixer can advantageously be:

• equal to that of the melting temperature of the crosslinking agent B, or
• at most equal to the melting temperature of the crosslinking agent B supplemented with 10 ° C., and preferably at most equal to the melting temperature of the crosslinking agent B plus 5 ° C.,

especially since the melting temperature of the polymer A is preferably lower than the melting temperature of the crosslinking agent B.

As a result, the crosslinking agent B can be homogeneously mixed with the polymer A, while significantly limiting, if not avoiding, any reaction of the crosslinking agent B with the polymer A.

By way of example, mention may be made of 1,3-PBO which has a melting point of about 148 ° C. As a result, the maximum extrusion and / or mixing temperature is preferably at most 158 ° C.

Step ii may be carried out thermally, for example by means of a continuous vulcanization line ("CV line"), a steam tube, a bath of molten salt, a furnace or a thermal chamber, these techniques being well known to those skilled in the art.

Step ii thus makes it possible to obtain a crosslinked layer, in particular having a gel level, according to ASTM D2765-01, of at least 40%, preferably at least 50%, preferably at least 60%, and particularly preferably at least 70%.

At the extruder outlet, the extruded composition in the form of a layer around the electrically conductive element can then be subjected to a sufficient temperature and for a sufficient time, in order to obtain the desired crosslinking, by reacting the reactive functions of the polymer A with open oxazoline functions. An extruded and crosslinked layer is then obtained.

1. i. mouler la composition polymère destinée à entourer un élément électriquement conducteur allongé, pour obtenir une couche moulée, et
2. ii. réticuler la couche moulée de l'étape i.

Another subject of the invention relates to a method of manufacturing an accessory for an electric cable, characterized in that it comprises the following steps:

1. i. molding the polymeric composition for surrounding an elongated electrically conductive member to provide a molded layer, and
2. ii. crosslink the molded layer of step i.

Step i may be carried out by techniques well known to those skilled in the art, in particular by molding or extrusion-molding.

Prior to step i, the constituent compounds of the polymer composition of the invention may be mixed as described above for the manufacture of a cable.

Step ii may be carried out thermally, for example using a heating mold, which may be the mold used in step i.

Stage ii thus makes it possible to obtain a crosslinked layer, in particular having a gel level, according to ASTM D2765-01, of at least 40%, preferably at least 50%, preferably at least 60%, and particularly preferably at least 70%.

In the mold, the composition of step i can then be subjected to a sufficient temperature and for a sufficient time, in order to obtain the desired crosslinking, by the reaction of the reactive functions of polymer A with the open oxazoline functions. A molded and crosslinked layer is then obtained.

In the present invention, the crosslinking temperature and the crosslinking time of the extruded and / or molded layer used are in particular functions of the thickness of the layer, the number of layers, the presence or absence of a crosslinking catalyst, etc.

Those skilled in the art can easily determine these parameters by following the evolution of the crosslinking by determining the gel level according to ASTM D2765-01 to obtain a crosslinked layer.

When an extruder is used, the temperature profile of the extruder and the extrusion rate are parameters on which the skilled person can also play to ensure the achievement of the desired properties.

Other features and advantages of the present invention will become apparent in the light of the description of non-limiting examples of an electric cable according to the invention and of an accessory for an electric cable according to the invention, made with reference to the figures.

The figure 1 is a schematic cross-sectional view of an electric cable according to a preferred embodiment according to the invention.

The figure 2 is a schematic view of an electrical device according to the invention, comprising a junction in longitudinal section, this junction surrounding the end of two electrical cables.

The figure 3 is a schematic view of an electrical device according to a first embodiment of the invention, comprising a longitudinal sectional termination, this termination surrounding the end of a single electrical cable.

For the sake of clarity, only the essential elements for understanding the invention have been shown schematically, and this without respect of the scale.

Medium or high voltage power cable 1, shown in FIG. figure 1 comprises an elongate central conductive element 2, in particular made of copper or aluminum. The energy cable 1 further comprises several layers arranged successively and coaxially around this conductive element 2, namely: a first semiconductor layer 3 called "internal semiconductor layer", an electrically insulating layer 4, a second layer Semiconductor semiconductor layer external ", a metal screen 6 for grounding and / or protection, and an outer protective sheath 7.

The electrically insulating layer 4 is an extruded and crosslinked layer obtained from the polymer composition according to the invention.

The semiconductor layers are also extruded and crosslinked layers, obtainable from the polymer composition according to the invention.

The presence of the metal screen 6 and the outer protective sheath 7 is preferred, but not essential, this cable structure being as such well known to those skilled in the art.

The figure 2 represents a device 101 comprising a junction 20 partially surrounding two electrical cables 10a and 10b.

More particularly, the electric cables 10a and 10b respectively comprise an end 10'a and 10'b, intended to be surrounded by the junction 20.

The body of the junction 20 comprises a first semiconductor element 21 and a second semiconductor element 22, separated by an electrically insulating element 23, said semiconductor elements 21, 22 and said electrically insulating element 23 surround the ends 10 ' a and 10'b respectively electric cables 10a and 10b.

This junction 20 makes it possible to electrically connect the first cable 10a to the second cable 10b, in particular thanks to an electrical connector 24 disposed at the center of the junction 20.

At least one of the elements selected from the first semiconductor element 21, the second semiconductor element 22 and said electrically insulating element 23 may be a crosslinked layer as described in the invention.

The first electrical cable 10a comprises an electrical conductor 2a surrounded by a first semiconductor layer 3a, an electrically insulating layer 4a surrounding the first semiconductor layer 3a, and a second semiconductor layer 5a surrounding the electrically insulating layer 4a.

The second electrical cable 10b comprises an electrical conductor 2b surrounded by at least a first semiconductor layer 3b, an electrically insulating layer 4b surrounding the first semiconductor layer 3b, and a second semiconductor layer 5b surrounding the electrically insulating layer 4b .

These electric cables 10a and 10b may be those described in the present invention.

At said end 10'a, 10'b of each electrical cable 10a, 10b, the second semiconductor layer 5a, 5b is at least partially stripped so that the electrically insulating layer 4a, 4b is at least partially positioned inside. of the junction 20, without being covered with the second semiconductor layer 5a, 5b of the cable.

Inside the junction 20, the electrically insulating layers 4a, 4b are directly in physical contact with the electrically insulating element 23 and the first semiconductor element 21 of the junction 20. The second semiconductor layers 5a, 5b are in direct physical contact with the second semiconductor element 22 of the junction 20.

The figure 3 represents a device 102 comprising a termination 30 surrounding a single electrical cable 10c.

More particularly, the electric cable 10c comprises an end 10'c, intended to be surrounded by the termination 30.

The body of the termination 30 comprises a semiconductor element 31 and an electrically insulating element 32, said semiconductor element 31 and said electrically insulating element 32 surround the end 10'c of the electric cable 10c.

At least one of the elements selected from the semiconductor element 31 and the electrically insulating element 32 may be a crosslinked layer as described in the invention.

The electrical cable 10c comprises an electrical conductor 2c surrounded by a first semiconductor layer 3c, an electrically insulating layer 4c surrounding the first semiconductor layer 3c, and a second semiconductor layer 5c surrounding the electrically insulating layer 4c.

This electric cable 10c may be that described in the present invention.

At said end 10'c of the electric cable 10c, the second semiconductor layer 5c is at least partially stripped so that the electrically insulating layer 4c is at least partially positioned inside the terminal 30, without being covered by the second semiconductor layer 5c of the cable.

Inside the termination 30, the electrically insulating layer 4c is directly in physical contact with the electrically insulating element 32 of the termination 30. The second semiconductor layer 5c is in direct physical contact with the semiconductor element. conductor 31 of the junction 30.

Examples of polymeric compositions according to the invention, to obtain an electrically insulating crosslinked layer

• 70-99.8% by weight of polymer A,
• 0.2-20% by weight of crosslinking agent B,
• 0-4% by weight of a crosslinking catalyst,
• 0-5% by weight of an antioxidant,
• 0-20% by weight of an oil,
• 0-5% by weight of an anti-tree water agent, and
• 0-5% by weight of agent for modifying the rate of crosslinking.

Examples of polymer compositions according to the invention, to obtain a semiconducting crosslinked layer

• 55-98% by weight of polymer A,
• 0.2-20% by weight of crosslinking agent B,
• 0-4% by weight of a crosslinking catalyst,
• 8-40% by weight of an electrically conductive filler of the carbon black type, with 0-5% by weight of carbon nanotubes,
• 0-5% by weight of an antioxidant,
• 0-20% by weight of an oil, and
• 0-5% by weight of agent for modifying the rate of crosslinking.

Characterization of the mechanical properties of uncharged electrically insulating compositions

Table 1 below collects uncharged polymer compositions, the amounts of the compounds are expressed as percentages (%) by weight in the polymer composition.

The polymer matrix in these polymer compositions comprises a single olefin A polymer (A1, A2, A3 or A4).

The compositions C1 to C6 are in accordance with the invention, while the composition Ref1 corresponds to a reference composition. <b><u> Table 1 </ u></b> compositions Polymer A1 (% by weight) Polymer A2 (% by weight) Polymer A3 (% by weight) Polymer A4 (% by weight) Agent B (% by weight) Catalyst (% by weight) Ref1 100 0 0 0 0 0 C1 94.0 0 0 0 6.0 0 C2 90.0 0 0 0 10.0 0 C3 93.0 0 0 0 6.0 1.0 C4 0 94.0 0 0 6.0 0 C5 0 0 94.0 0 6.0 0 C6 0 0 0 94.0 6.0 0

• Polymère A1 est un copolymère d'éthylène et d'acide méthacrylique, commercialisé par la société Dupont sous la référence Nucrel^® 0910. Ce copolymère comprend environ 8,6 % en poids de fonctions carboxyles, a une température de fusion (i.e. état fondu) de l'ordre de 100°C, et a un indice de fluidité de 10 en gramme/10 minutes, selon la norme ASTM D 1238 à 190°C/2,16 kg.
• Polymère A2 est un copolymère d'éthylène et d'acide acrylique, commercialisé par la société Dow sous la référence Primacor^® 3150. Ce copolymère comprend environ 3,0 % en poids de fonctions carboxyles, a une température de fusion (i.e. état fondu) de l'ordre de 104 °C, et a un indice de fluidité de 11 en gramme/10 minutes, selon la norme ASTM D 1238 à 190°C/2,16 kg.
• Polymère A3 est un copolymère d'éthylène et d'acide acrylique, com m ercialisé par la société Dow sous la référence Primacor^® 3340. Ce copolymère comprend environ 6,5 % en poids de fonctions carboxyles, a une température de fusion (i.e. état fondu) de l'ordre de 101 °C, et a un indice de fluidité de 9 en gramme/10 minutes, selon la norme ASTM D 1238 à 190°C/2,16 kg.
• Polymère A4 est un copolymère d'éthylène et d'acide acrylique, commercialisé par la société Dow sous la référence Primacor^® 3440. Ce copolymère comprend environ 9,7 % en poids de fonctions carboxyles, a une température de fusion (i.e. état fondu) de l'ordre de 98 °C, et a un indice de fluidité de 10 en gramme/10 minutes, selon la norme ASTM D 1238 à 190°C/2,16 kg.
• Agent B est l'agent de réticulation 1,3-PBO ayant une température de fusion de l'ordre de 148°C.
• Catalyseur est un catalyseur de réticulation du type DBTL, commercialisé par la société Solvay Padanaplast, sous la référence Catalyst CT/5.

The origin of the compounds of Table 1 is as follows:

• Polymer A1 is a copolymer of ethylene and methacrylic acid, sold by DuPont under the reference Nucrel ^® 0910. This copolymer comprises about 8.6% by weight of carboxyl groups, has a melting temperature (ie melt) of the order of 100 ° C, and has a melt index of 10 gram / 10 minutes, according to ASTM D 1238 at 190 ° C / 2.16 kg.
• Polymer A2 is a copolymer of ethylene and acrylic acid, commercially available from Dow under the reference Primacor ^® 3150. This copolymer comprises about 3.0% by weight of carboxyl groups, has a melting temperature (ie melt) of the order of 104 ° C, and has a melt index of 11 gram / 10 minutes, according to ASTM D 1238 at 190 ° C / 2.16 kg.
• Polymer A3 is a copolymer of ethylene and acrylic acid, com m ercialisé by Dow under the reference Primacor ^® 3340. This copolymer comprises about 6.5% by weight of carboxyl groups, has a melting temperature (ie state melted) of the order of 101 ° C, and has a melt index of 9 gram / 10 minutes, according to ASTM D 1238 at 190 ° C / 2.16 kg.
• A4 polymer is a copolymer of ethylene and acrylic acid, commercially available from Dow under the reference Primacor ^® 3440. This copolymer comprises about 9.7% by weight of carboxyl groups, has a melting temperature (ie melt) of the order of 98 ° C, and has a melt index of 10 gram / 10 minutes, according to ASTM D 1238 at 190 ° C / 2.16 kg.
• Agent B is the 1.3-PBO crosslinking agent having a melting temperature of the order of 148 ° C.
• Catalyst is a crosslinking catalyst of the DBTL type, sold by Solvay Padanaplast under the reference Catalyst CT / 5.

The compositions summarized in Table 1 are implemented as follows.

In a first step, for each composition (C1 to C6), the crosslinking agent B is mixed with the polymer A in the molten state, in a single-screw Brabender type extruder.

The length of the screw is 475 mm, and its diameter is 19 mm (i.e. L = 25D).

The temperature profile of the extruder is shown in Table 2 below. <u> Table 2 </ u> compositions Speed (m / min) Zone 1 introduction (° C) Zone 2 (° C) Zone 3 (° C) Zone 4 at the extruder outlet (° C) Ref1 0.8 148 158 165 164 C1 1.03 149 166 164 160 C2 1.03 149 166 164 160 C3 1.07 166 182 178 186 C4 1.03 145 157 164 168 C5 1.03 145 157 164 168 C6 1.03 145 157 164 168

The speed shown in Table 2 is the extrusion speed.

The compositions of Table 1 are thus extruded into a ribbon layer, according to the extrusion characteristics mentioned in Table 2. The thickness of the ribbons is 2.0 mm.

Of course, the extrusion may advantageously be carried out in a layer surrounding an elongated electrically conductive element to form a cable, but the characterization of the mechanical properties (electrically insulating compositions not loaded according to the invention) in ribbon form is sufficient.

At the exit of the extruder, the extruded layers C1 to C6 in ribbon form are not crosslinked, and have a gel level of the order 0%.

Since the extruded layer Ref1 does not comprise a crosslinking agent, it can not be crosslinked.

In a second step, the extruded layers C1 to C6 are crosslinked by heat input.

According to a first variant (V1), the extruded layers C1 to C3 in the form of a ribbon are crosslinked at a temperature of at least 90 ° C. for several hours, in particular for 24 hours. More particularly, the C1 to C3 extruded layers are crosslinked for 6 hours at 95 ° C. and then for 18 hours at 115 ° C., at atmospheric pressure, using a standard oven marketed by Heraeus.

According to a second variant (V2), the extruded layers C1 to C3 in the form of a ribbon are crosslinked at a temperature of 70.degree. C. for several hours, in particular for 117 hours, at atmospheric pressure, using a standard oven. marketed by Heraeus.

According to a third variant (V3), the extruded layers C4 to C6 in the form of ribbon are, in turn, crosslinked at a temperature of 280 ° C for a few minutes, especially for 5 minutes. More particularly, the extruded layers C4 to C6 are crosslinked for 3 minutes at 280 ° C. under 0 bar, then for 2 minutes at 280 ° C. under 10 bar, at room temperature. using a conventional heating press. They are then cooled for 2 minutes under 10 bar.

• le taux de gel réalisé selon la norme ASTM D2765-01 avec une extraction au xylène,
• les résultats des tests de résistance à la traction réalisés selon la norme NF EN 60811-1-1,
• les résultats des tests d'allongement à la rupture réalisés selon la norme NF EN 60811-1-1, et
• les résultats de fluage à chaud sous charge et de rémanence, selon la norme NF EN 60811-2-1.

Table 3 below shows:

• gel level achieved according to ASTM D2765-01 with xylene extraction,
• the results of the tensile strength tests carried out according to standard NF EN 60811-1-1,
• the results of elongation at break tests carried out according to standard NF EN 60811-1-1, and
• the results of hot creep under load and remanence, according to standard NF EN 60811-2-1.

The standard NF EN 60811-2-1 describes the measurement of the hot flow of a material under load. The corresponding test is commonly designated by the Anglicism "Hot Set Test". It concretely consists of ballasting one end of a test piece of material with a mass corresponding to the application of a stress equivalent to 0.2 MPa, and placing the assembly in an oven heated to 200 +/- 1 ° C. a duration of 15 minutes. At the end of this period, the hot elongation under load of the test piece, expressed in%, is recorded. The suspended mass is then removed, and the test piece is kept in the oven for another 5 minutes. The remaining permanent elongation, also called remanence, is then measured before being expressed in%. It is recalled that the more a material is crosslinked, the longer the values of elongation and remanence will be low. It is also specified that in the case where a test piece breaks during the test, under the combined action of the mechanical stress and the temperature, the test result would then logically be considered a failure.

In the present invention, the tensile strength is preferably at least 12.5 N / mm ² , and the elongation at break is preferably at least 200%, these mechanical properties being determined according to the standard NF EN 60811-1-1.

In the present invention, the hot elongation under load is preferably less than 175%, and the remanence is preferably less than 15%, these properties being determined according to standard NF EN 60811-2-1. <b><u> Table 3 </ u></b> compositions Ref1 C1 C2 C3 Cross-linking: Variant V1 Frost rate (%) 0 93 93 92 Tensile strength (N / mm ² ) 24.5 22.1 21.1 19.8 Elongation at break (%) 499 257 263 236 Elongation at break (%) under load Failure 20 10 20 Remanence (%) Failure 0 0 0 compositions C1 C2 C3 Crosslinking: Variant V2 Tensile strength (N / mm ² ) 28.2 28.8 22.7 Elongation at break (%) 347 339 263 Elongation at break (%) under load 10 15 10 Remanence (%) 0 0 0 compositions C4 C5 C6 Cross-linking: Variant V3 Frost rate (%) 92 93 96 Tensile strength (N / mm ² ) 18.8 18.2 18.8 Elongation at break (%) 383 222 193 Elongation at break (%) under load 20 10 10 Remanence (%) 0 0 0

It is clear that the layers of the invention are perfectly crosslinked, while having very good mechanical properties such as tensile strength and elongation at break, the latter being greater than 200%.

Claims (21)

Electrical device (1,20,30) comprising a crosslinked layer (3,4,5,21,22,23,31,32) for surrounding or surrounding an elongated electrically conductive element, characterized in that the crosslinked layer is obtained from a polymer composition comprising: at least one olefin polymer (A), and a crosslinking agent (B) comprising one or more oxazoline functions,
the polymer A comprising one or more reactive functional groups capable of reacting with the oxazoline function of the crosslinking agent B. Device according to claim 1, characterized in that the polymer composition comprises more than 50 parts by weight of polymer A per 100 parts by weight of polymer (s) in the composition. Device according to claim 1 or 2, characterized in that the polymer A is not a polyacrylate. Device according to any one of the preceding claims, characterized in that the polymer A is not a polyimide. Device according to any one of the preceding claims, characterized in that the reactive function is a carboxyl function. Device according to any one of the preceding claims, characterized in that the polymer A comprises at most 20% by weight of reactive function relative to the total weight of the polymer A. Device according to any one of the preceding claims, characterized in that the polymer A is an olefin polymer comprising said reactive functions grafted onto the macromolecular chain of said polymer. Device according to any one of the preceding claims, characterized in that the polymer A is an olefin copolymer and a monomer bearing the reactive function. Device according to claim 8, characterized in that the polymer A is a copolymer of ethylene and acrylic or methacrylic acid. Device according to any one of the preceding claims, characterized in that the polymer composition comprises at least 40% by weight of polymer A relative to the total weight of the polymer composition. Device according to any one of the preceding claims, characterized in that the crosslinking agent is a polymeric compound or a non-polymeric compound. Device according to claim 11, characterized in that the polymeric compound is a copolymer functionalized with oxazoline functions. Device according to claim 11, characterized in that the nonpolymeric compound comprises at least two oxazoline functions. Device according to Claim 13, characterized in that the non-polymeric compound is chosen from 2,2 '- (1,3-phenylene) bis (2-oxazoline), 2,2' - (1,4-phenylene) bis (2-oxazoline) and 2,2 '- (2,6-pyridylene) bis (2-oxazoline). Device according to any one of the preceding claims, characterized in that the composition comprises less than 10 parts by weight of fluoropolymer per 100 parts by weight of polymer (s) in the composition. Device according to any one of the preceding claims, characterized in that the crosslinked layer is chosen from a layer electrically insulating, a semiconductor layer, a stuffing element, and a protective sheath. Device according to any one of the preceding claims, characterized in that it is an electric cable (1) comprising said crosslinked layer surrounding the elongated electrically conductive element (2). Device according to claim 17, characterized in that the crosslinked layer is an extruded layer. Device according to claim 17 or 18, characterized in that it comprises a first semiconductor layer (3) surrounding the elongated electrically conductive element (2), an electrically insulating layer (4) surrounding the first semiconductor layer ( 3), and a second semiconductor layer (5) surrounding the electrically insulating layer (4), the crosslinked layer being at least one of these three layers. Device according to any one of claims 1 to 16, characterized in that it is an accessory (20,30) for electric cable, intended to surround or surrounding an elongated electrically conductive element of an electric cable, comprising the crosslinked layer (21,22,23,31,32). A method of manufacturing an electric cable (1) according to any one of claims 17 to 19, characterized in that the method comprises the following steps: i. extruding the polymer composition around the elongate electrically conductive member, to obtain an extruded layer, and ii. crosslink the extruded layer of step i.

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