Flame-retardant polycarbonate molding materials ii
US-2015307705-A1 · Oct 29, 2015 · US
US12552904B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12552904-B2 |
| Application number | US-202017637838-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 27, 2020 |
| Priority date | Sep 4, 2019 |
| Publication date | Feb 17, 2026 |
| Grant date | Feb 17, 2026 |
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The invention relates to a polyphosphazene produced by a method comprising the steps a) and b): a) converting an in particular cyclical phosphazene by means of phenol in the presence of a base; b) further converting by means of a special aromatic diphenol in the presence of a base, wherein the molar ratio of phenol used to cyclical phosphazene used is in the range from 3.5:1 to 1:1. The invention also relates to a method for producing the polyphosphazene and to a molding compound containing the polyphosphazene and a thermoplastic polymer.
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The invention claimed is: 1 . A polyphosphazene produced by a process comprising the steps a) and b): a) reaction of a cyclic phosphazene of formula (1) wherein k is a natural number between 1 and 10 with phenol in the presence of a base; and b) further reaction with an aromatic diphenol of formula (2) wherein R 1 and R 2 independently of one another represent H or C 1 - to C 8 -alkyl and X represents a single bond, C 1 - to C 5 -alkylene, C 2 - to C 5 -alkylidene, C 5 - to C 6 -cycloalkylidene, —O—, —SO—, —CO—, —S—, or —SO 2 — in the presence of a base, wherein the molar ratio of employed phenol to the employed cyclic phosphazene of formula (1) is in the range from 3.5:1 to 1:1, and wherein the molar ratio of employed phenol to the employed aromatic diphenol of formula (2) is in the range from 3:1 to 1:1. 2 . The polyphosphazene as claimed in claim 1 , characterized in that the phosphazene has a swelling factor Q = a - b b of 1 to 15 after storage for 3 days in chloroform, wherein a is the mass of the swollen polyphosphazene and b is the mass of the unswollen polyphosphazene. 3 . The polyphosphazene as claimed claim 1 , characterized in that the base employed in steps a) and b) is selected from 1,8-diazabicyclo[5.4.0]undec-7-ene, N,N-diethylethanamine, and 1,5,7-triazabicyclo[4.4.0]dec-5-ene. 4 . The polyphosphazene as claimed in claim 1 , characterized in that the polyphosphazene has a glass transition temperature determined by differential scanning calorimetry of 70° C. to 150° C. 5 . The polyphosphazene as claimed in claim 1 , characterized in that the employed cyclic phosphazene of formula (1) is a compound having a trimer proportion (k=1) of 60 to 100 mol % based on the cyclic phosphazene of formula (1). 6 . The polyphosphazene as claimed in claim 1 , characterized in that 2,2-bis(4-hydroxyphenyl) propane is used as the aromatic diphenol according to formula (2). 7 . A molding compound containing a thermoplastic polymer and a polyphosphazene as claimed in claim 1 . 8 . The molding compound as claimed in claim 7 , characterized in that the thermoplastic polymer is a polyester, polycarbonate, vinyl (co) polymer, polyamide or mixtures thereof. 9 . The molding compound as claimed in claim 7 , characterized in that the polyphosphazene is present in a proportion of 2% to 20% by weight. 10 . A molded article containing a molding compound as claimed in claim 7 . 11 . The polyphosphazene as claimed in claim 1 , characterized in that in step a) the base is added in a molar ratio of 0.8:1 to 1.2:1 based on phenol and in step b) in a molar ratio of 0.8:1 to 1.2:1 based on the OH groups of the diphenol. 12 . The polyphosphazene as claimed in claim 1 , wherein the molar ratio of employed phenol to the employed aromatic diphenol of formula (2) is in the range from 3:1 to 1.2:1. 13 . The polyphosphazene as claimed in claim 1 , wherein the molar ratio of employed phenol to the employed aromatic diphenol of formula (2) is in the range from 2:1 to 1.2:1.
Compositions of polycarbonates; Compositions of derivatives of polycarbonates · CPC title
Polyphosphazenes · CPC title
Cyclic phosphazenes [P=N-]n, n>=3 · CPC title
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