Polysulfone copolymer with excellent heat resistance and chemical resistance, and method for preparing same
US-2017240708-A1 · Aug 24, 2017 · US
US12098244B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12098244-B2 |
| Application number | US-202017594169-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 3, 2020 |
| Priority date | Apr 5, 2019 |
| Publication date | Sep 24, 2024 |
| Grant date | Sep 24, 2024 |
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The invention relates to a process for producing semi-aromatic polyethers based on an aliphatic diol, to semi-aromatic polyethers based on an aliphatic diol obtained by said process, and to the use of said semi-aromatic polyethers based on an aliphatic diol for manufacturing membranes, manufactured parts and coatings.
Opening claim text (preview).
The invention claimed is: 1. A semi-aromatic polyether based on an aliphatic diol of formula I: wherein Ar originates from a dihalogenated aromatic or heteroaromatic compound selected from dihalogenated aromatic sulfones, dihalogenated aromatic ketones, dihalogenated benzonitriles, dihalogenated diazenes, bis(halophenyl)oxadiazoles, dihalogenated nitrobenzenes, dihalogenated benzoylnaphthalenes and dihalogenated pyridines; R originates from an aliphatic diol; X is a chlorine; n is an integer between 2 and 100, with n being determined by size-exclusion chromatography; provided that R does not originate from isosorbide, cyclohexanedimethanol, tetramethylcyclobutanediol, or cis-1,5-cyclooctanediol when Ar originates from a 4,4′-halodiphenyl sulfone, and that R does not originate from isosorbide when Ar originates from a 4,4′-dihalobenzophenone; wherein the semi-aromatic polyether based on an aliphatic diol contains residual silicon content of between 10 and 1,000 ppm, said residual silicon content being determined by combustion/ion chromatography coupling. 2. The semi-aromatic polyether based on an aliphatic diol according to claim 1 , wherein R originates from an aliphatic diol selected from linear aliphatic diols and branched aliphatic diols. 3. The semi-aromatic polyether based on an aliphatic diol according to claim 1 , wherein R originates from a 1,4:3,6-dianhydrohexitol. 4. The semi-aromatic polyether based on an aliphatic diol according to claim 1 , wherein its polydispersity index is between 1.5 and 5. 5. The semi-aromatic polyether based on an aliphatic diol according to claim 1 , wherein its number-average molecular weight is greater than or equal to 5,000 g/mol, said number-average molecular weight being measured by size-exclusion chromatography in dimethylformamide at 70° C. with a flow rate of 0.7 mL/min and with polystyrene calibration. 6. The semi-aromatic polyether based on an aliphatic diol according to claim 1 , wherein it has a glass transition temperature of greater than 100° C. 7. The semi-aromatic polyether based on an aliphatic diol according to claim 1 , wherein it contains a residual fluorine content of less than 100 ppm, said residual fluorine content being determined by combustion/ion chromatography coupling. 8. The semi-aromatic polyether based on an aliphatic diol according to claim 1 , wherein it contains a residual chlorine content of between 100 and 10,000 ppm, said residual chlorine content being determined by combustion/ion chromatography coupling.
Aromatic polyethers · CPC title
Monomer containing functional groups not involved in polymerisation · CPC title
containing ketone groups, e.g. polyarylethylketones, PEEK or PEK · CPC title
Sugars or saccharides used as initiators · CPC title
Polyethersulfones · CPC title
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