FI65790C - Flexibla och/eller i organiska loesningsmedel loesliga p-oxibenzoylsampolyestrar laempliga foer press- och ytbelaeggningsprodukter - Google Patents

Flexibla och/eller i organiska loesningsmedel loesliga p-oxibenzoylsampolyestrar laempliga foer press- och ytbelaeggningsprodukter Download PDF

Info

Publication number: FI65790C
Authority: FI; Finland
Prior art keywords: ratio; polyester; mixed; structural unit; meta
Prior art date: 1978-11-09

Application number

FI793407A

Other languages

English (en)

Finnish (fi)

Swedish (sv)

Other versions

FI65790B (fi

FI793407A7 (fi

Inventor

Roger S Storm

Original Assignee

Dart Ind Inc

Priority date (The priority date 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 date listed.)

1978-11-09

Filing date

1979-10-31

Publication date

1984-07-10

1979-10-31 Application filed by Dart Ind Inc filed Critical Dart Ind Inc

1980-05-10 Publication of FI793407A7 publication Critical patent/FI793407A7/fi

1984-03-30 Publication of FI65790B publication Critical patent/FI65790B/fi

1984-07-10 Application granted granted Critical

1984-07-10 Publication of FI65790C publication Critical patent/FI65790C/fi

Links

229920000728 polyester Polymers 0.000 claims description 81
229920000642 polymer Polymers 0.000 claims description 26
238000000576 coating method Methods 0.000 claims description 22
229920001343 polytetrafluoroethylene Polymers 0.000 claims description 18
239000004810 polytetrafluoroethylene Substances 0.000 claims description 18
-1 polytetrafluoroethylene Polymers 0.000 claims description 17
239000011248 coating agent Substances 0.000 claims description 16
239000003960 organic solvent Substances 0.000 claims description 12
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 8
125000004430 oxygen atom Chemical group O* 0.000 claims description 7
229910052717 sulfur Inorganic materials 0.000 claims description 7
239000000758 substrate Substances 0.000 claims description 2
125000004434 sulfur atom Chemical group 0.000 claims 6
239000006223 plastic coating Substances 0.000 claims 1
230000003678 scratch resistant effect Effects 0.000 claims 1
239000000047 product Substances 0.000 description 30
FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 20
238000002360 preparation method Methods 0.000 description 20
239000007858 starting material Substances 0.000 description 19
150000001875 compounds Chemical class 0.000 description 18
239000002904 solvent Substances 0.000 description 15
239000000243 solution Substances 0.000 description 14
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
238000006243 chemical reaction Methods 0.000 description 12
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 12
239000011347 resin Substances 0.000 description 12
229920005989 resin Polymers 0.000 description 12
239000000203 mixture Substances 0.000 description 11
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 10
150000002148 esters Chemical class 0.000 description 10
BLDLRWQLBOJPEB-UHFFFAOYSA-N 2-(2-hydroxyphenyl)sulfanylphenol Chemical group OC1=CC=CC=C1SC1=CC=CC=C1O BLDLRWQLBOJPEB-UHFFFAOYSA-N 0.000 description 9
229940090248 4-hydroxybenzoic acid Drugs 0.000 description 9
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 9
239000004020 conductor Substances 0.000 description 9
239000006185 dispersion Substances 0.000 description 9
125000003118 aryl group Chemical group 0.000 description 8
125000001931 aliphatic group Chemical group 0.000 description 7
238000009835 boiling Methods 0.000 description 7
238000000034 method Methods 0.000 description 7
239000011541 reaction mixture Substances 0.000 description 7
QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 6
VWGKEVWFBOUAND-UHFFFAOYSA-N 4,4'-thiodiphenol Chemical compound C1=CC(O)=CC=C1SC1=CC=C(O)C=C1 VWGKEVWFBOUAND-UHFFFAOYSA-N 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
239000002253 acid Substances 0.000 description 5
238000007906 compression Methods 0.000 description 5
230000006835 compression Effects 0.000 description 5
229920001577 copolymer Polymers 0.000 description 5
238000004519 manufacturing process Methods 0.000 description 5
VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
229920001634 Copolyester Polymers 0.000 description 4
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
125000000217 alkyl group Chemical group 0.000 description 4
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
238000002156 mixing Methods 0.000 description 4
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
150000005690 diesters Chemical class 0.000 description 3
230000032050 esterification Effects 0.000 description 3
238000005886 esterification reaction Methods 0.000 description 3
150000002170 ethers Chemical class 0.000 description 3
238000000605 extraction Methods 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
239000000178 monomer Substances 0.000 description 3
239000002245 particle Substances 0.000 description 3
239000007921 spray Substances 0.000 description 3
150000001911 terphenyls Chemical class 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
239000005711 Benzoic acid Substances 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
150000001491 aromatic compounds Chemical class 0.000 description 2
125000004429 atom Chemical group 0.000 description 2
235000010233 benzoic acid Nutrition 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
235000010290 biphenyl Nutrition 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
239000000084 colloidal system Substances 0.000 description 2
239000002131 composite material Substances 0.000 description 2
239000002612 dispersion medium Substances 0.000 description 2
239000000835 fiber Substances 0.000 description 2
HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 2
239000000155 melt Substances 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
239000012299 nitrogen atmosphere Substances 0.000 description 2
150000002989 phenols Chemical group 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
229920005604 random copolymer Polymers 0.000 description 2
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
238000005245 sintering Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 2
239000008096 xylene Substances 0.000 description 2
MHCVCKDNQYMGEX-UHFFFAOYSA-N 1,1'-biphenyl;phenoxybenzene Chemical compound C1=CC=CC=C1C1=CC=CC=C1.C=1C=CC=CC=1OC1=CC=CC=C1 MHCVCKDNQYMGEX-UHFFFAOYSA-N 0.000 description 1
BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
PFHTYDZPRYLZHX-UHFFFAOYSA-N 2-(2,5-dihydroxyphenyl)benzene-1,4-diol Chemical compound OC1=CC=C(O)C(C=2C(=CC=C(O)C=2)O)=C1 PFHTYDZPRYLZHX-UHFFFAOYSA-N 0.000 description 1
GOWCECVOTUONTI-UHFFFAOYSA-N 3-(3-hydroxyphenyl)sulfanylphenol Chemical compound OC1=CC=CC(SC=2C=C(O)C=CC=2)=C1 GOWCECVOTUONTI-UHFFFAOYSA-N 0.000 description 1
SKWKXBZGGSUEBW-UHFFFAOYSA-N 3-(4-hydroxyphenyl)sulfanylphenol Chemical compound C1=CC(O)=CC=C1SC1=CC=CC(O)=C1 SKWKXBZGGSUEBW-UHFFFAOYSA-N 0.000 description 1
TWPCOQWVKILGIN-UHFFFAOYSA-N 4-(2-methylpropoxycarbonyl)benzoic acid Chemical compound CC(C)COC(=O)C1=CC=C(C(O)=O)C=C1 TWPCOQWVKILGIN-UHFFFAOYSA-N 0.000 description 1
NZGQHKSLKRFZFL-UHFFFAOYSA-N 4-(4-hydroxyphenoxy)phenol Chemical compound C1=CC(O)=CC=C1OC1=CC=C(O)C=C1 NZGQHKSLKRFZFL-UHFFFAOYSA-N 0.000 description 1
SGPZSOQUJLFTMQ-UHFFFAOYSA-N 4-o-ethyl 1-o-methyl benzene-1,4-dicarboxylate Chemical compound CCOC(=O)C1=CC=C(C(=O)OC)C=C1 SGPZSOQUJLFTMQ-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
229910000640 Fe alloy Inorganic materials 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
239000004809 Teflon Substances 0.000 description 1
229920006362 Teflon® Polymers 0.000 description 1
238000012644 addition polymerization Methods 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000007824 aliphatic compounds Chemical class 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
239000003849 aromatic solvent Substances 0.000 description 1
150000008378 aryl ethers Chemical class 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
238000005452 bending Methods 0.000 description 1
235000019445 benzyl alcohol Nutrition 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
125000006267 biphenyl group Chemical group 0.000 description 1
150000004074 biphenyls Chemical class 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000006482 condensation reaction Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
150000001896 cresols Chemical class 0.000 description 1
JLVWYWVLMFVCDI-UHFFFAOYSA-N diethyl benzene-1,3-dicarboxylate Chemical compound CCOC(=O)C1=CC=CC(C(=O)OCC)=C1 JLVWYWVLMFVCDI-UHFFFAOYSA-N 0.000 description 1
FHESUNXRPBHDQM-UHFFFAOYSA-N diphenyl benzene-1,3-dicarboxylate Chemical compound C=1C=CC(C(=O)OC=2C=CC=CC=2)=CC=1C(=O)OC1=CC=CC=C1 FHESUNXRPBHDQM-UHFFFAOYSA-N 0.000 description 1
HPGJOUYGWKFYQW-UHFFFAOYSA-N diphenyl benzene-1,4-dicarboxylate Chemical compound C=1C=C(C(=O)OC=2C=CC=CC=2)C=CC=1C(=O)OC1=CC=CC=C1 HPGJOUYGWKFYQW-UHFFFAOYSA-N 0.000 description 1
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000000374 eutectic mixture Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical compound O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 description 1
150000005165 hydroxybenzoic acids Chemical class 0.000 description 1
238000001746 injection moulding Methods 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
230000002045 lasting effect Effects 0.000 description 1
125000005647 linker group Chemical group 0.000 description 1
238000010309 melting process Methods 0.000 description 1
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
125000000612 phthaloyl group Chemical group C(C=1C(C(=O)*)=CC=CC1)(=O)* 0.000 description 1
229920002959 polymer blend Polymers 0.000 description 1
229920006389 polyphenyl polymer Polymers 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
239000011253 protective coating Substances 0.000 description 1
238000007670 refining Methods 0.000 description 1
239000013557 residual solvent Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000010959 steel Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
230000002194 synthesizing effect Effects 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
- C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/68—Unsaturated polyesters
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
- C08G18/7614—Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring
- C08G18/7621—Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring being toluene diisocyanate including isomer mixtures
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
- C08G63/688—Polyesters containing atoms other than carbon, hydrogen and oxygen containing sulfur
- C08G63/6882—Polyesters containing atoms other than carbon, hydrogen and oxygen containing sulfur derived from hydroxy carboxylic acids
- G—PHYSICS
- G05—CONTROLLING; REGULATING
- G05B—CONTROL OR REGULATING SYSTEMS IN GENERAL; FUNCTIONAL ELEMENTS OF SUCH SYSTEMS; MONITORING OR TESTING ARRANGEMENTS FOR SUCH SYSTEMS OR ELEMENTS
- G05B11/00—Automatic controllers
- G05B11/01—Automatic controllers electric
- G05B11/012—Automatic controllers electric details of the transmission means
- G05B11/016—Automatic controllers electric details of the transmission means using inductance means
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F29/00—Variable transformers or inductances not covered by group H01F21/00
- H01F29/14—Variable transformers or inductances not covered by group H01F21/00 with variable magnetic bias
- H—ELECTRICITY
- H03—ELECTRONIC CIRCUITRY
- H03F—AMPLIFIERS
- H03F9/00—Magnetic amplifiers
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/3154—Of fluorinated addition polymer from unsaturated monomers
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
- Y10T428/31681—Next to polyester, polyamide or polyimide [e.g., alkyd, glue, or nylon, etc.]
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
- Y10T428/31692—Next to addition polymer from unsaturated monomers
- Y10T428/31699—Ester, halide or nitrile of addition polymer
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31786—Of polyester [e.g., alkyd, etc.]

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Power Engineering (AREA)
Physics & Mathematics (AREA)
Automation & Control Theory (AREA)
General Physics & Mathematics (AREA)
Polyesters Or Polycarbonates (AREA)
Paints Or Removers (AREA)

FI793407A 1978-11-09 1979-10-31 Flexibla och/eller i organiska loesningsmedel loesliga p-oxibenzoylsampolyestrar laempliga foer press- och ytbelaeggningsprodukter FI65790C (fi)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US95927578		1978-11-09
US05/959,275 US4219629A (en)	1978-11-09	1978-11-09	P-Oxybenzoyl copolyesters comprising thiodiphenol components and having improved flexibility and solubility in organic solvents

Publications (3)

Publication Number	Publication Date
FI793407A7 FI793407A7 (fi)	1980-05-10
FI65790B FI65790B (fi)	1984-03-30
FI65790C true FI65790C (fi)	1984-07-10

Family

ID=25501865

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
FI793407A FI65790C (fi)	1978-11-09	1979-10-31	Flexibla och/eller i organiska loesningsmedel loesliga p-oxibenzoylsampolyestrar laempliga foer press- och ytbelaeggningsprodukter

Country Status (29)

Country	Link
US (1)	US4219629A (de)
JP (1)	JPS5566924A (de)
AR (1)	AR218561A1 (de)
AT (1)	AT383605B (de)
AU (1)	AU519289B2 (de)
BE (1)	BE879936A (de)
BR (1)	BR7907240A (de)
CA (1)	CA1129586A (de)
CH (1)	CH643274A5 (de)
DE (1)	DE2945370C3 (de)
DK (1)	DK472879A (de)
ES (1)	ES8103763A1 (de)
FI (1)	FI65790C (de)
FR (1)	FR2441638A1 (de)
GB (1)	GB2035347B (de)
GR (1)	GR66809B (de)
IE (1)	IE49111B1 (de)
IL (1)	IL58613A (de)
IT (1)	IT1209132B (de)
LU (1)	LU81879A1 (de)
MA (1)	MA18637A1 (de)
NL (1)	NL186173C (de)
NO (1)	NO150121C (de)
NZ (1)	NZ192016A (de)
PH (1)	PH18753A (de)
PL (1)	PL128087B1 (de)
PT (1)	PT70434A (de)
SE (1)	SE440661B (de)
ZA (1)	ZA795796B (de)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5594930A (en) *	1979-01-10	1980-07-18	Sumitomo Chem Co Ltd	Preparation of aromatic polyester by improved bulk polymerization process
JPS55149321A (en) *	1979-05-11	1980-11-20	Sumitomo Chem Co Ltd	Preparation of oxybenzoylcopolyester
IE54564B1 (en) *	1982-07-26	1989-11-22	Dart Ind Inc	Polyester moulding compositions and ovenware therefrom
US4626557A (en) *	1982-07-26	1986-12-02	Dart Industries, Inc.	Plastic ovenware containing talc
US4510205A (en) *	1983-05-26	1985-04-09	Eastman Kodak Company	Copolyesterethers coated with saran
US4606930A (en) *	1984-03-02	1986-08-19	Sumitomo Chemical Company, Limited	Method for treating fibers
JPS61199821A (ja) *	1985-03-01	1986-09-04	住友化学工業株式会社	非粘着性を有するプラスチックオ−ブンウエア
US5015723A (en) *	1988-09-02	1991-05-14	Sumitomo Chemical Company, Limited	Process for producing aromatic polyesters
JP2847188B2 (ja) *	1988-11-04	1999-01-13	住友化学工業株式会社	芳香族ポリエステルの製造方法
US5173562A (en) *	1990-10-29	1992-12-22	Chisso America Inc.	Liquid crystal polymer composition containing bisphenol A in combination with 4,4'-thiodiphenol
CN115746281B (zh) *	2022-11-04	2024-05-14	东华大学	一种热致液晶聚合物及其制备方法和应用

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2600376A (en) *	1949-11-26	1952-06-17	Eastman Kodak Co	Polmesters of hydroxybenzoic acids
US2728747A (en) *	1952-10-22	1955-12-27	Gen Mills Inc	Polyester resins
US3216970A (en) *	1956-12-14	1965-11-09	Gevaert Photo Prod Nv	Production of linear aromatic polyesters containing isophthalic acid
GB907647A (en) *	1960-02-29	1962-10-10	Ici Ltd	New aromatic polyesters
US3240735A (en) *	1961-09-14	1966-03-15	Eastman Kodak Co	Thermoplastic polyesters of bisphenols and dicarboxylic acids having increased modulus of elasticity due to presence of stiffness improving additives
US3310601A (en) *	1963-06-20	1967-03-21	Shell Oil Co	Curing polyepoxides with a mixture of difunctional and polyfunctional mercaptans
US3640965A (en) *	1968-10-02	1972-02-08	Union Carbide Corp	Thermoplastic sulfur-containing polymers
US3637595A (en) *	1969-05-28	1972-01-25	Steve G Cottis	P-oxybenzoyl copolyesters
US3644593A (en) *	1969-05-28	1972-02-22	Carborundum Co	Compositions of matter comprising oxybenzoyl polyesters and polyfluorinated addition polymers
US3600350A (en) *	1970-04-20	1971-08-17	Du Pont	Poly(p-benzamide) composition,process and product
US3857814A (en) *	1970-12-08	1974-12-31	Carborundum Co	Branched aromatic polyesters and cross-linked derivatives thereof
US3873502A (en) *	1972-04-18	1975-03-25	Dow Chemical Co	Cycloaliphatic polythiols and compositions containing same
JPS5629703B2 (de) *	1973-04-03	1981-07-10
JPS505443A (de) *	1973-05-18	1975-01-21
US3972852A (en) *	1973-08-07	1976-08-03	Teijin Limited	Process for preparing aromatic polyesters from diphenols
US4102864A (en) *	1976-02-02	1978-07-25	Monsanto Company	Polyesters of 1,2-bis(hydroxyphenyl) ethanes and aromatic dicarboxylic acids

1978
- 1978-11-09 US US05/959,275 patent/US4219629A/en not_active Expired - Lifetime
1979
- 1979-10-29 ZA ZA00795796A patent/ZA795796B/xx unknown
- 1979-10-31 FI FI793407A patent/FI65790C/fi not_active IP Right Cessation
- 1979-10-31 AU AU52366/79A patent/AU519289B2/en not_active Ceased
- 1979-11-02 IL IL5861379A patent/IL58613A/xx unknown
- 1979-11-02 NZ NZ19201679A patent/NZ192016A/xx unknown
- 1979-11-02 AR AR27874679A patent/AR218561A1/es active
- 1979-11-03 GR GR60410A patent/GR66809B/el unknown
- 1979-11-05 PH PH23240A patent/PH18753A/en unknown
- 1979-11-07 PL PL1979219467A patent/PL128087B1/pl unknown
- 1979-11-07 JP JP14427679A patent/JPS5566924A/ja active Granted
- 1979-11-08 NO NO793604A patent/NO150121C/no unknown
- 1979-11-08 CH CH1001279A patent/CH643274A5/de not_active IP Right Cessation
- 1979-11-08 BR BR7907240A patent/BR7907240A/pt unknown
- 1979-11-08 GB GB7938666A patent/GB2035347B/en not_active Expired
- 1979-11-08 ES ES485810A patent/ES8103763A1/es not_active Expired
- 1979-11-08 DK DK472879A patent/DK472879A/da not_active Application Discontinuation
- 1979-11-08 MA MA18838A patent/MA18637A1/fr unknown
- 1979-11-08 IT IT2714279A patent/IT1209132B/it active
- 1979-11-08 SE SE7909263A patent/SE440661B/sv not_active IP Right Cessation
- 1979-11-08 CA CA339,482A patent/CA1129586A/en not_active Expired
- 1979-11-09 LU LU81879A patent/LU81879A1/fr unknown
- 1979-11-09 DE DE2945370A patent/DE2945370C3/de not_active Expired
- 1979-11-09 PT PT7043479A patent/PT70434A/pt unknown
- 1979-11-09 IE IE2151/79A patent/IE49111B1/en unknown
- 1979-11-09 NL NL7908241A patent/NL186173C/xx not_active IP Right Cessation
- 1979-11-09 FR FR7927755A patent/FR2441638A1/fr active Granted
- 1979-11-09 BE BE0/198049A patent/BE879936A/fr not_active IP Right Cessation
- 1979-11-09 AT AT721279A patent/AT383605B/de not_active IP Right Cessation

Also Published As

Publication number	Publication date
IL58613A0 (en)	1980-02-29
AT383605B (de)	1987-07-27
CH643274A5 (de)	1984-05-30
NO150121B (no)	1984-05-14
ZA795796B (en)	1981-07-29
NO793604L (no)	1980-05-12
SE440661B (sv)	1985-08-12
NL186173B (nl)	1990-05-01
GB2035347A (en)	1980-06-18
NL7908241A (nl)	1980-05-13
SE7909263L (sv)	1980-05-10
GB2035347B (en)	1982-11-24
PL128087B1 (en)	1983-12-31
PL219467A1 (de)	1980-12-01
JPS5645930B2 (de)	1981-10-29
DE2945370A1 (de)	1980-05-14
IL58613A (en)	1982-11-30
MA18637A1 (fr)	1980-07-01
PT70434A (en)	1979-12-01
AR218561A1 (es)	1980-06-13
NZ192016A (en)	1981-04-24
LU81879A1 (fr)	1980-04-22
NL186173C (nl)	1990-10-01
ATA721279A (de)	1986-12-15
PH18753A (en)	1985-09-19
BE879936A (fr)	1980-03-03
AU5236679A (en)	1980-05-15
FI65790B (fi)	1984-03-30
ES485810A0 (es)	1981-03-16
IE792151L (en)	1980-05-09
BR7907240A (pt)	1980-07-08
FR2441638A1 (fr)	1980-06-13
DE2945370C3 (de)	1982-04-01
DE2945370B2 (de)	1981-05-21
ES8103763A1 (es)	1981-03-16
GR66809B (de)	1981-04-30
FI793407A7 (fi)	1980-05-10
FR2441638B1 (de)	1984-12-28
IT7927142A0 (it)	1979-11-08
US4219629A (en)	1980-08-26
IT1209132B (it)	1989-07-10
JPS5566924A (en)	1980-05-20
IE49111B1 (en)	1985-08-07
DK472879A (da)	1980-05-10
NO150121C (no)	1984-08-22
CA1129586A (en)	1982-08-10
AU519289B2 (en)	1981-11-19

Legal Events

Date	Code	Title	Description
2004-08-31	MM	Patent lapsed	Owner name: DART INDUSTRIES INC

Publication	Publication Date	Title
KR920007527B1 (ko)	1992-09-05	혼합 폴리아미드 올리고머
CA1142685A (en)	1983-03-08	Aromatic copolyester
US3946091A (en)	1976-03-23	Aromatic co-polyester articles showing reduced crazing
EP0060531A1 (de)	1982-09-22	Verfahren zur Herstellung einer Zusammensetzung auf Basis eines aromatischen Polyesters
JPS60197759A (ja)	1985-10-07	ポリイミド樹脂組成物
US20210189064A1 (en)	2021-06-24	Polyisoindolinones, methods of manufacture, and compositions and articles formed therefrom
US4219629A (en)	1980-08-26	P-Oxybenzoyl copolyesters comprising thiodiphenol components and having improved flexibility and solubility in organic solvents
US10640645B2 (en)	2020-05-05	Polyisoindolinone compositions, methods of manufacture, and compositions and articles formed therefrom
JP6505829B2 (ja)	2019-04-24	結晶性全芳香族ポリエステルおよびその製造方法
JP3095412B2 (ja)	2000-10-03	ポリ（アリールエーテル）とのポリカーボネート及び／又はポリアリーレートブロックコポリマー並びにそれらの製造方法
Yang et al.	1990	Preparation and properties of polyarylates from 5‐t‐butylisophthaloyl chloride and various bisphenols
PL141794B1 (en)	1987-08-31	Method of obtaining unsaturated polyester resins
Chiou et al.	2008	Synthesis and studies of the physical properties of polyaniline and polyurethane‐modified epoxy composites
EP1165649A1 (de)	2002-01-02	Verfahren zur herstellung von polyketonen
JP7770309B2 (ja)	2025-11-14	ポリアミド－イミドポリマー、ポリマー組成物、及びそれらを含む物品、並びにそれらの製造方法
KR850000616B1 (ko)	1985-05-01	옥시벤조일 코폴리 에스테르류의 제조방법
JP2015187214A (ja)	2015-10-29	ワニスおよびその製造方法
Gui et al.	2013	Preparation and thermal stability of amine-terminated polyesterimide modified epoxy resin
EP0445409A2 (de)	1991-09-11	Estergruppen enthaltende aromatische Polyether
Abd-Alla	1990	Arylidene Polymers VIII. Synthesis, Characterization and Morphology of New Polyesters Based on 2, 7-Diarylidenecycloheptanone
WO2021048075A1 (en)	2021-03-18	Polyamide-imide polymer and process for its manufacture
DE2549528A1 (de)	1977-05-18	Verfahren zur herstellung sulfongruppenhaltiger polyarylate
JP2022146906A (ja)	2022-10-05	繊維用集束剤、繊維束、繊維製品、樹脂組成物及び成形体
JPH0379375B2 (de)	1991-12-18
JPH0512394B2 (de)	1993-02-17