DE1795664C3 - Process for the preparation of aqueous polytetrafluoroethylene dispersions and their use - Google Patents
Process for the preparation of aqueous polytetrafluoroethylene dispersions and their useInfo
- Publication number
- DE1795664C3 DE1795664C3 DE19681795664 DE1795664A DE1795664C3 DE 1795664 C3 DE1795664 C3 DE 1795664C3 DE 19681795664 DE19681795664 DE 19681795664 DE 1795664 A DE1795664 A DE 1795664A DE 1795664 C3 DE1795664 C3 DE 1795664C3
- Authority
- DE
- Germany
- Prior art keywords
- parts
- polytetrafluoroethylene
- dispersion
- aqueous
- colloidal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000006185 dispersion Substances 0.000 title claims 15
- -1 polytetrafluoroethylene Polymers 0.000 title claims 13
- 229920001343 polytetrafluoroethylene Polymers 0.000 title claims 12
- 239000004810 polytetrafluoroethylene Substances 0.000 title claims 12
- 238000000034 method Methods 0.000 title claims 6
- BFKJFAAPBSQJPD-UHFFFAOYSA-N Tetrafluoroethylene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims 6
- 238000004519 manufacturing process Methods 0.000 claims 6
- 230000002429 anti-coagulation Effects 0.000 claims 5
- 239000003146 anticoagulant agent Substances 0.000 claims 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 4
- 150000002148 esters Chemical class 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- 229920000151 polyglycol Polymers 0.000 claims 4
- 239000010695 polyglycol Substances 0.000 claims 4
- UUAGAQFQZIEFAH-UHFFFAOYSA-N Chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 claims 3
- XUCNUKMRBVNAPB-UHFFFAOYSA-N Vinyl fluoride Chemical group FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 claims 3
- 229920001577 copolymer Polymers 0.000 claims 3
- 238000006116 polymerization reaction Methods 0.000 claims 3
- PLLBRTOLHQQAQQ-UHFFFAOYSA-N 8-methylnonan-1-ol Chemical compound CC(C)CCCCCCCO PLLBRTOLHQQAQQ-UHFFFAOYSA-N 0.000 claims 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N Ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 claims 2
- 239000005977 Ethylene Substances 0.000 claims 2
- 239000004440 Isodecyl alcohol Substances 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 2
- 238000001246 colloidal dispersion Methods 0.000 claims 2
- 239000004815 dispersion polymerization Substances 0.000 claims 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 2
- 238000001125 extrusion Methods 0.000 claims 2
- ARUVKPQLZAKDPS-UHFFFAOYSA-L Copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims 1
- 229920000126 Latex Polymers 0.000 claims 1
- 241001182492 Nes Species 0.000 claims 1
- 229940053207 Niacin Drugs 0.000 claims 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N Nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 claims 1
- 239000004721 Polyphenylene oxide Substances 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 239000000701 coagulant Substances 0.000 claims 1
- 230000001112 coagulant Effects 0.000 claims 1
- 238000005345 coagulation Methods 0.000 claims 1
- 230000015271 coagulation Effects 0.000 claims 1
- 238000007334 copolymerization reaction Methods 0.000 claims 1
- 229910000365 copper sulfate Inorganic materials 0.000 claims 1
- 235000014113 dietary fatty acids Nutrition 0.000 claims 1
- 239000003995 emulsifying agent Substances 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 239000000194 fatty acid Substances 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 claims 1
- 238000005755 formation reaction Methods 0.000 claims 1
- 239000011953 free-radical catalyst Substances 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 1
- 239000004816 latex Substances 0.000 claims 1
- 230000004048 modification Effects 0.000 claims 1
- 238000006011 modification reaction Methods 0.000 claims 1
- DFPAKSUCGFBDDF-UHFFFAOYSA-N nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims 1
- 229960003512 nicotinic acid Drugs 0.000 claims 1
- 235000001968 nicotinic acid Nutrition 0.000 claims 1
- 239000011664 nicotinic acid Substances 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- 229920000570 polyether Polymers 0.000 claims 1
- 229920001522 polyglycol ester Polymers 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 238000001556 precipitation Methods 0.000 claims 1
- 238000000926 separation method Methods 0.000 claims 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 238000011105 stabilization Methods 0.000 claims 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N vinyl chloride Chemical group ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Claims (2)
•ind vor allem die als Emulgatoren in Handel erhältlichen Produkte geeignet, vorzugsweise Alkyl- 45 Beispiel
phenol-polyglykoläther, wie Nonylphenol-polyglykol-drive for the production of aqueous polytetrafluoroethylene possible to increase the proportion of a submitted, so modified ^ dispersions by polymerization of tetra- 3 ° decorated seed dispersion up to 25%, without using fuoräthylen in aqueous dispersion with the help of free that a disruptive coagulation occurs. This avoids catalysts which form free radicals and in the presence of the complex separation of coagulate from the initially charged colloidal polytetrafluoroethylene and excellent stabilization of the obtained and anticoagulants, with dispersion being achieved. In particular, the inventively improved, colloidal polytetrafluoroethylene-containing process according to the invention has advantages for the subsequent precipitation of the dispersion, which is stable in aqueous polytetrafluoroethylene dispersions, for use in paste extrusion which is obtained as an anticoagulant: of 2 nes result in a more uniform grain of the precipitated to 60 parts per million parts of the total mixture of product with a further reduced grain diameter used. Preferably, the polyoxyalkylenates 40 ser. The excellent quality of or their esters can thus be used in quantities of 5 to 15 parts per paste extrudate from polytetra million parts of the total mixture modified in this way. Improve even further by fluoroethylene dispersions. the numerous polyalkylates and their esters
• Ind especially suitable as emulsifiers commercially available products, preferably alkyl 45 example
phenol polyglycol ethers, such as nonylphenol polyglycol
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19671720738 DE1720738C (en) | 1967-10-21 | 1967-10-21 | Process for the production of aqueous polytetrafluoroethylene dispersions and their use for the production of paste extrudates |
DE19681795664 DE1795664C3 (en) | 1968-09-20 | Process for the preparation of aqueous polytetrafluoroethylene dispersions and their use |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF0053862 | 1967-10-21 | ||
DE19681795664 DE1795664C3 (en) | 1968-09-20 | Process for the preparation of aqueous polytetrafluoroethylene dispersions and their use |
Publications (3)
Publication Number | Publication Date |
---|---|
DE1795664A1 DE1795664A1 (en) | 1973-04-26 |
DE1795664B2 DE1795664B2 (en) | 1976-01-02 |
DE1795664C3 true DE1795664C3 (en) | 1976-08-26 |
Family
ID=
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