IP Library Granted Patent US 9,884,961
Granted Patent B2
US 9,884,961 · App. 15/033,986 · Granted Feb 6, 2018

Phosphazene flame retardant polycarbonate compounds

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Quick Facts
Patent No.
US 9,884,961
App. No.
15/033,986
Granted
Feb 6, 2018
Kind
B2
Abstract

A non-halogenated flame retardant polycarbonate compound is disclosed. The compound comprises a polycarbonate, a non-halogenated, non-migrating, non-plasticizing flame retardant adduct. The compound can achieve a UL 94 rating of V-0 at a thickness of at least 3.2 mm and otherwise achieves no dripping/igniting of the cotton indicator during that test. The adduct is formed from an allyl-functional phenoxyphosphazene and a hydride-functional polysiloxane.

Claims (38)

1. A flame retardant polycarbonate compound, comprising:

(a) polycarbonate homopolymer or copolymer,

(b) a crosslinked phosphorous-containing silicone formed without solvent from an allyl-functional phenoxyphosphazene derivative and a hydride-functional siloxane.

2. The compound of claim 1 , wherein the hydride-functional siloxane comprises a homopolymer or copolymer of methyl hydrosiloxane moieties, and/or hydride terminated poly-disubstituted siloxanes, which optionally contain phenyl and other alkyl substitution, in linear, cyclic, or oligomeric configuration.

3. The compound of claim 1 , wherein the polycarbonate is a combination of linear polycarbonate and branched carbonate.

4. The compound of claim 1 , wherein the hydride functional siloxane is poly(methyl hydrosiloxane) homopolymer or methylhydrosiloxane-dimethylsiloxane copolymer, or both, in which the percentage of methylhydrosiloxane and/or hydride terminal poly-dimethyl siloxane moieties can range from about 1 to about 99 weight percent.

5. The compound of claim 1 , further comprising talc.

6. The compound of claim 1 , further comprising a second non-halogenated flame retardant.

7. The compound of claim 6 , wherein the second non-halogenated flame retardant is selected from the group consisting of bisphosphate esters, polyphosphonates, polyphosphazenes, and combinations thereof.

8. The compound of claim 1 , wherein the reaction of the allyl-functional phenoxyphosphazene derivative and a hydride-functional siloxane occurs in situ during melt mixing with the polycarbonate via hydrosilylation with a platinum catalyst.

9. The compound of claim 8 , wherein the compound when injection molded and tested at a thickness of 3.2 mm passes the dripping/igniting portion of UL 94 test.

10. The compound of claim 9 , wherein the allyl-functional phenoxyphosphazene comprises

(a) cyclic phosphazenes of Formula (1)

wherein m is an integer of 3 to 25, two R 1 groups are the same or different and each represents a phenyl group substituted with at least one group selected from the class consisting of alkyl groups having 1 to 6 carbon atoms and an allyl group or an unsubstituted phenyl group, or a hydroxy substituted phenyl or

(b) straight-chain phosphazenes of Formula (2)

wherein n is an integer of 3 to 1000, R 1 is as defined above, X represents a group —N=P(OR 1 ) 3 or a group —N=P(O)OR 1 , and Y represents a group —P(OR 1 ) 4 or a group—P(O)(OR 1 ) 2 or

combinations thereof.

11. The compound of claim 1 , further comprising adhesion promoters; biocides; anti-fogging agents; anti-static agents; bonding, blowing or foaming agents; dispersants; fillers or extenders; smoke suppressants; impact modifiers; initiators; lubricants; micas; colorants; plasticizers; impact modifiers; processing aids; release agents; silanes; titanates; zirconates; slip or anti-blocking agents; stabilizers; stearates; ultraviolet light absorbers; viscosity regulators; waxes; catalyst deactivators; or combinations of them.

12. The compound of claim 1 , wherein the polycarbonate homopolymer is a mixture of a branched polycarbonate of virginal source, recycled source, or both, and a linear polycarbonate of virginal source, recycled source, or both and wherein the polycarbonate copolymer is polyphosphonate-co-carbonate.

13. The compound of claim 11 , wherein the compound has ingredients in amounts expressed in weight percent:

Polycarbonate Matrix

  50-99.9

Allyl functional phenoxyphosphazene

0.1-25 

Hydride-functional Polysiloxane

0.1-25 

Platinum Catalyst Complex (1-2.5% Platinum)

0.01-1  

Optional Non-Halogenated Char Former

0-2

Optional Talc

0-9

Optional Non-Halogenated Flame Retardant

 0-10

Optional Other Additives

 0-5.

14. A shaped article made from the compound of claim 1 , wherein the shaping occurs by extrusion, molding, calendering, thermoforming, and additive manufacturing.

15. A method of using the compound of claim 1 , comprising the step of shaping the compound into an article designed to resist combustion or molten dripping in the presence of flame.

Assignments (5)
RELEASE OF SECURITY INTERESTS IN PATENTS RECORDED AT REEL 041373, FRAME 0454. Recorded Jun 24, 2025
From: WELLS FARGO CAPITAL FINANCE, LLC, AS ADMINISTRATIVE AGENT
To: AVIENT CORPORATION (F/K/A POLYONE CORPORATION); COLORMATRIX HOLDINGS, INC.; GSDI SPECIALTY DISPERSIONS, INC.
Reel/Frame 071708/0258 →
SECURITY AGREEMENT Recorded Jun 12, 2025
From: AVIENT CORPORATION; COLORMATRIX HOLDINGS, INC.; COLORMATRIX GROUP, INC.
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 071574/0571 →
PATENT SECURITY AGREEMENT (TERM) Recorded Jun 12, 2024
From: AVIENT CORPORATION; COLORMATRIX HOLDINGS, INC.
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 067699/0676 →
CHANGE OF NAME Recorded Jul 13, 2020
From: POLYONE CORPORATION
To: AVIENT CORPORATION
Reel/Frame 053197/0141 →
SECURITY INTEREST Recorded Feb 24, 2017
From: POLYONE CORPORATION; COLORMATRIX HOLDINGS, INC.; GSDI SPECIALTY DISPERSIONS, INC.; POLYONE DESIGNED STRUCTURES AND SOLUTIONS LLC
To: WELLS FARGO CAPITAL FINANCE, LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 041373/0454 →