IP Library Granted Patent US 11,932,746
Granted Patent B2
US 11,932,746 · App. 15/039,849 · Granted Mar 19, 2024

Composition

Inventors: Jonathan Hill (Trafford Park, GB); Siren Tan (Trafford Park, GB); Christopher Rider (Trafford Park, GB)
Assignee: SI Group, Inc.
C08K5/005B29B7/88B29C48/022B29C48/154C08K5/0025C08K5/13C08K5/14C08K5/36C09K15/14H01B3/30H01B7/2813H01B13/148B29K2995/0005B29K2995/0007B29L2031/3462C08K2201/014
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Quick Facts
Patent No.
US 11,932,746
App. No.
15/039,849
Granted
Mar 19, 2024
Kind
B2
Abstract

The present invention relates to stabilising compositions, particularly stabilising compositions which can be used to stabilise insulation or semi-conductive compositions, such as are used for electrically insulating wires and cables. The stabilising composition comprises: a first stabilising component comprising at least one fully hindered phenolic antioxidant; a second stabilising component comprising at least one partially hindered phenolic antioxidant; and a third stabilising component comprising at least one sulphur-containing antioxidant.

Claims (14)

1. A stabilising composition for a polyethylene homopolymer or copolymer, comprising:

a. a first stabilising component consisting of one or more of C13-C15 linear and branched alkyl esters of 3-(3′5′-di-t-butyl-4′-hydroxyphenyl) propionic acid;

b. a second stabilising component consisting of 6-tert-butyl-2-methylphenol; and

c. a third stabilising component consisting of ditridecylthiodipropionate;

wherein the stabilising composition has a melting point of about 30C or lower, at atmospheric pressure of 101.325 kPa, and

wherein

the first stabilising component (a) is present in an amount ranging from about 25% to about 29% by weight of the stabilising composition,

the second stabilising component (b) is present in an amount ranging from about 14% to about 25% by weight of the stabilising composition,

the third stabilising component (c) is present in an amount ranging from about 50% to about 57% by weight of the stabilising composition.

2. The stabilising composition according to claim 1 , further comprising at least one low-hindered phenolic antioxidant and/or at least one non-hindered phenolic antioxidant.

3. The stabilising composition according to claim 1 further comprising octadecyl3-(3′,5′-di-t-butyl-4′-hydroxyphenyl) propionate; N,N′-hexamethylene bis[3-(3,5-di-t-butyl-4-hydroxyphenyl)propionamide]; C9-C11linear and branched alkyl esters of 3-(3′,5′-di-t-butyl-4′-hydroxyphenyl)propionic acid; butylated hydroxytoluene; 2,6-di-tertiary -butyl-4-sec-butylphenol; 2,6-di-tertiary-butyl-4-nonylphenol; tetrakismethylene(3,5-di-t-butyl-4-hydroxyhydrocinnamate) methane; 1,3,5-tris(3,5-di-t-butyl-4-hydroxybenzyl) isocyanurate; 1,2-bis (3,5-di-t-butyl-4-hydroxyhydrocinnamoyl)hydrazine; 2, 2′thiodiethylene bis [3(3,5 -di-t-butyl-4-hydroxyphenyl)propionate]; 1,3,5-trimethyl-2,4,6-tris(3,5-di-t-butyl-4-hydroxybenzyl)benzene; butylated hydroxytoluene; or mixtures of two or more thereof.

4. The stabilising composition according to claim 1 further comprising 2,4-bis(n-octylthiomethyl)-6-methylphenol; pentaerythritol tetrakis ((β-laurylthiopropionate); dilauryl-3,3′-thiodipropionate; distearyl-3,3′-thiodipropionate; 2, 2′thiodiethylene bis[3(3,5-di-t-butyl-4-hydroxyphenyl)propionate]; dimyristyl thiodipropionate; distearyl-disulfide; or mixtures of two or more thereof.

5. The stabilising composition according to claim 1 wherein the stabilising composition is food contact compliant.

6. The stabilising composition according to claim 1 further comprising 2-(1,1-dimethylethyl)-4,6-dimethyl-phenol; 6-tert-butyl-2-methylphenol; 4,6-di-tert-butyl-2-methylphenol, 2-tert-butyl-4-methylphenol; 2-tert-butyl-5-methylphenol; 2,4-di-tert-butyl phenol; 2,4-di-tert-pentylphenol; triethyleneglycol-bis-[3-(3-t-butyl-4-hydroxy-5-methyl phenyl)propionate]; 1,3,5-tris(4-t-butyl-3-hydroxyl-2,6-dimethylbenzyl)-1,3,5-triazine -2,4,6-(1H, 3H, 5H)-trione; 2,2′-ethylidenebis[4,6-di-t-butylphenol]; 2,2′methylenebis(6-t-butyl-4-methylphenol); or mixtures of two or more thereof.

Assignments (10)
RELEASE OF SECURITY INTEREST Recorded Dec 30, 2025
From: ALTER DOMUS (US) LLC, AS COLLATERAL AGENT
To: SI GROUP, INC.
Reel/Frame 074136/0039 →
ASSIGNMENT OF SECURITY INTEREST IN PATENTS [REEL 068968/FRAME 0001] Recorded Dec 24, 2024
From: JPMORGAN CHASE BANK, N.A.
To: ALTER DOMUS (US) LLC
Reel/Frame 069770/0736 →
RELEASE OF SECURITY INTEREST Recorded Nov 1, 2024
From: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
To: SI GROUP, INC.; ADDIVANT USA, LLC; SI GROUP USA (USAA), LLC (F/K/A ADDIVANT USA, LLC)
Reel/Frame 069290/0057 →
SECURITY INTEREST Recorded Sep 19, 2024
From: SI GROUP, INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 068968/0001 →
SECURITY INTEREST Recorded Sep 19, 2024
From: SI GROUP, INC.
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 068968/0024 →
MERGER Recorded Feb 16, 2023
From: SI GROUP USA (USAA), LLC
To: SI GROUP, INC.
Reel/Frame 062719/0326 →
CORRECTIVE ASSIGNMENT TO CORRECT THE MERGER AND CHANGE OF NAME SHOULD BE CORRECTED TO CHANGE OF NAME PREVIOUSLY RECORDED ON REEL 050635 FRAME 0880. ASSIGNOR(S) HEREBY CONFIRMS THE AMENDED AND RESTATED CERTIFICATE OF FORMATION OF ADDIVANT USA LLC. Recorded Oct 22, 2019
From: ADDIVANT USA LLC
To: SI GROUP USA (USAA), LLC
Reel/Frame 050784/0361 →
MERGER AND CHANGE OF NAME Recorded Oct 3, 2019
From: ADDIVANT USA, LLC; SI GROUP USA (USAA), LLC
To: SI GROUP USA (USAA), LLC
Reel/Frame 050635/0880 →
SECURITY INTEREST Recorded Nov 16, 2018
From: SI GROUP, INC.; ADDIVANT USA, LLC
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 048822/0965 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2016
From: HILL, JONATHAN; TAN, SIREN; RIDER, CHRISTOPHER
To: ADDIVANT USA LLC
Reel/Frame 040246/0001 →