Cable comprising crosslinked layer obtained from polymer composition

US11636959B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11636959-B2
Application numberUS-201916408622-A
CountryUS
Kind codeB2
Filing dateMay 10, 2019
Priority dateMay 10, 2018
Publication dateApr 25, 2023
Grant dateApr 25, 2023

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A cable is provided having at least one elongated conductor surrounded by at least one cross-linked layer, said layer being obtained from a polymer composition comprising a polymer, a crosslinking agent, and an amine as co-crosslinking agent, wherein said amine has a nucleophilic value (N) of 14 or more.

First claim

Opening claim text (preview).

The invention claimed is: 1. A cable comprising: at least one elongated conductor surrounded by at least one cross-linked layer, said layer being obtained from a polymer composition having a polymer, a crosslinking agent, and an amine as co-crosslinking agent, wherein said amine is a tertiary amine with a nucleophilic value (N) of 16 or more, wherein the crosslinking agent in the polymer composition is a polycarboxylic acid; wherein the polymer is [a polymer containing one or several carboxyl group(s) or] a polymer containing one or several epoxy group(s); wherein the polymer composition comprises the tertiary amine in an amount of from 0.1 parts by weight or more to 1 parts by weight or less, with respect to 100 parts by weight of the polymer; and wherein the polymer composition comprises the crosslinking agent in an amount of from 0.5 parts by weight or more to 5 parts by weight or less, with respect to 100 parts by weight of the polymer. 2. The cable according to claim 1 , wherein the amine is at least one selected from: monocyclic or bicyclic amine selected from 1,4-diazabicyclo[2.2.2]octane (DABCO), quinuclidine, piperidine, N-methylpiperidine, pyrrolidine, and N-methylpyrrolidine; guanidines selected from 1,5,7-Triazabicyclo[4.4.0]dec-5-ene (TBD), and 1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyrimidine (TBN); or monocyclic or bicyclic amidine bases including 1,5-diazabicyclo[4.3.0]non-5-ene (DBN). 3. The cable according to claim 1 , wherein the polycarboxylic acid is selected from: a′) aliphatic compounds selected from the group consisting of adipic acid, azelaic acid, citric acid, dodecanoic acid, itaconic acid, malic acid, maleic acid, sebacic acid, succinic acid, succinic anhydride; b′) cyclic compounds selected from the group consisting of 1,4-cyclohexanedicarboxylic acid, cis-4-cyclohexene-1,2-dicarboxylic acid; c′) aromatic compounds selected from the group consisting of 1,3,5-benzenetricarboxylic acid, isophthalic acid, phthalic acid, terephthalic acid, trimellitic acid, phthalic anhydride, and trimellitic anhydride; d′) polymers containing two or more carboxyl groups or maleic anhydrides in main chain, branch or terminal of the polymer and having molecular weight of 10,000 g/mol or less; or e′) a mixture of two or more selected from said a′) to d′). 4. The cable according to claim 1 , wherein the polymer composition further comprises an organometallic compound. 5. The cable according to claim 4 , wherein said organometallic compound is selected from the group consisting of dibutyltin dilaurate and bismuth-based carboxylate. 6. The cable according to claim 1 , wherein it is an electric power cable. 7. The cable according to claim 1 , wherein said selection of said crosslinking agent and said tertiary amine as co-crosslinking agent results in a crosslinking speed that is faster than using a polyamine as crosslinking agent and an amine having a nucleophilic value more than 16 as co-crosslinking agent or faster than using said crosslinking agent and an amine having a nucleophilic value less than 16 as co-crosslinking agent. 8. The cable according to claim 1 , wherein said selection of said crosslinking agent and said tertiary amine as co-crosslinking agent results in a crosslinking degree that is higher than using a polyamine as crosslinking agent and an amine having a nucleophilic value more than 16 as co-crosslinking agent or higher than using said crosslinking agent and an amine having a nucleophilic value less than 16 as co-crosslinking agent. 9. The cable according to claim 1 , wherein said at least one cross-linked layer is used as any one of an insulating layer, a semi-conductive layer, and a coating or sheath layer in said cable, said at least one cross-linked layer being halogen free. 10. The cable according to claim 1 , wherein the polymer has a molecular weight of greater than 5,000 g/mol. 11. The cable according to claim 1 , wherein the polymer has a molecular weight of 1,000,000 g/mol or less. 12. The cable according to claim 1 , wherein said polymer containing one or several epoxy group(s) contains from 0.1% by weight or more to 30% by weight or less, based on the total weight of the polymer, of repeating units comprising said epoxy groups. 13. The cable according to claim 1 , wherein said tertiary amine is bicyclic.

Assignees

Inventors

Classifications

  • Three-membered rings · CPC title

  • use in electrical wires or wirecoating · CPC title

  • Non-saturated polyesters derived from polycarboxylic acids and polyhydroxy compounds, in which at least one of the two components contains aliphatic unsaturation · CPC title

  • Ethylene vinyl acetate copolymers · CPC title

  • H01B3/441Primary

    from alkenes · CPC title

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What does patent US11636959B2 cover?
A cable is provided having at least one elongated conductor surrounded by at least one cross-linked layer, said layer being obtained from a polymer composition comprising a polymer, a crosslinking agent, and an amine as co-crosslinking agent, wherein said amine has a nucleophilic value (N) of 14 or more.
Who is the assignee on this patent?
Nexans
What technology area does this patent fall under?
Primary CPC classification H01B3/441. Mapped technology areas include Electricity.
When was this patent published?
Publication date Tue Apr 25 2023 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 5 related publications on this page (citations in our corpus or others sharing the same primary CPC).