LU81879A1 - Copolyesters de p-oxybenzoyle et produits les comprenant - Google Patents

Copolyesters de p-oxybenzoyle et produits les comprenant Download PDF

Info

Publication number: LU81879A1
Authority: LU; Luxembourg
Prior art keywords: copolyester; polyester; order; value; copolyesters
Prior art date: 1978-11-09

Application number

LU81879A

Other languages

English (en)

French (fr)

Inventor

R 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

1979-11-09

Publication date

1980-04-22

1979-11-09 Application filed by Dart Ind Inc filed Critical Dart Ind Inc

1980-04-22 Publication of LU81879A1 publication Critical patent/LU81879A1/fr

Links

229920001634 Copolyester Polymers 0.000 claims description 60
238000000576 coating method Methods 0.000 claims description 25
229920000728 polyester Polymers 0.000 claims description 23
229920000642 polymer Polymers 0.000 claims description 22
-1 polytetrafluoroethylene Polymers 0.000 claims description 20
239000011248 coating agent Substances 0.000 claims description 17
229920001343 polytetrafluoroethylene Polymers 0.000 claims description 17
239000004810 polytetrafluoroethylene Substances 0.000 claims description 17
239000012634 fragment Substances 0.000 claims description 14
239000003960 organic solvent Substances 0.000 claims description 9
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 7
229910052717 sulfur Inorganic materials 0.000 claims description 5
125000004429 atom Chemical group 0.000 claims description 4
125000004430 oxygen atom Chemical group O* 0.000 claims description 4
125000004434 sulfur atom Chemical group 0.000 claims description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
239000011593 sulfur Substances 0.000 claims description 2
230000003252 repetitive effect Effects 0.000 claims 1
230000003678 scratch resistant effect Effects 0.000 claims 1
239000000047 product Substances 0.000 description 22
238000004519 manufacturing process Methods 0.000 description 19
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 18
239000002904 solvent Substances 0.000 description 17
FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 15
239000000243 solution Substances 0.000 description 14
238000006243 chemical reaction Methods 0.000 description 12
150000001875 compounds Chemical class 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
239000003153 chemical reaction reagent Substances 0.000 description 11
BLDLRWQLBOJPEB-UHFFFAOYSA-N 2-(2-hydroxyphenyl)sulfanylphenol Chemical compound OC1=CC=CC=C1SC1=CC=CC=C1O BLDLRWQLBOJPEB-UHFFFAOYSA-N 0.000 description 10
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 10
239000002253 acid Substances 0.000 description 10
239000006185 dispersion Substances 0.000 description 10
238000000034 method Methods 0.000 description 10
239000000203 mixture Substances 0.000 description 10
125000003118 aryl group Chemical group 0.000 description 9
229940090248 4-hydroxybenzoic acid Drugs 0.000 description 7
238000009835 boiling Methods 0.000 description 7
229920001577 copolymer Polymers 0.000 description 7
150000002148 esters Chemical class 0.000 description 7
239000000376 reactant Substances 0.000 description 7
239000000463 material Substances 0.000 description 6
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
125000001931 aliphatic group Chemical group 0.000 description 5
238000001035 drying Methods 0.000 description 5
238000000605 extraction 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
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 4
239000007795 chemical reaction product Substances 0.000 description 4
150000005690 diesters Chemical class 0.000 description 4
238000002156 mixing Methods 0.000 description 4
239000002245 particle Substances 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
239000011541 reaction mixture Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
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
150000002170 ethers Chemical class 0.000 description 3
229910052739 hydrogen Inorganic materials 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
238000002347 injection Methods 0.000 description 3
239000007924 injection Substances 0.000 description 3
239000000155 melt Substances 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
239000000178 monomer Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
150000001911 terphenyls Chemical class 0.000 description 3
RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 3
239000005711 Benzoic acid Substances 0.000 description 2
241000790917 Dioxys <bee> Species 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
239000004809 Teflon Substances 0.000 description 2
229920006362 Teflon® Polymers 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
125000000217 alkyl group Chemical group 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
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
230000015572 biosynthetic process Effects 0.000 description 2
235000010290 biphenyl Nutrition 0.000 description 2
239000000084 colloidal system Substances 0.000 description 2
238000007334 copolymerization reaction Methods 0.000 description 2
238000005336 cracking Methods 0.000 description 2
239000000835 fiber Substances 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
238000001746 injection moulding Methods 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
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 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
238000001556 precipitation Methods 0.000 description 2
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000007921 spray Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 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
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
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
229920013807 TRITON DF-12 Polymers 0.000 description 1
238000012644 addition polymerization Methods 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
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
235000019445 benzyl alcohol Nutrition 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
125000006267 biphenyl group Chemical group 0.000 description 1
VCCBEIPGXKNHFW-UHFFFAOYSA-N biphenyl-4,4'-diol Chemical group C1=CC(O)=CC=C1C1=CC=C(O)C=C1 VCCBEIPGXKNHFW-UHFFFAOYSA-N 0.000 description 1
150000004074 biphenyls Chemical class 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000007810 chemical reaction solvent 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
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
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
230000005496 eutectics Effects 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
150000005165 hydroxybenzoic acids Chemical class 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
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
238000010309 melting process Methods 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
150000002989 phenols Chemical group 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
229920006389 polyphenyl polymer Polymers 0.000 description 1
239000011253 protective coating Substances 0.000 description 1
238000010298 pulverizing process Methods 0.000 description 1
238000005488 sandblasting Methods 0.000 description 1
238000002791 soaking Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000010959 steel Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000009466 transformation Effects 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003739 xylenols Chemical class 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)

LU81879A 1978-11-09 1979-11-09 Copolyesters de p-oxybenzoyle et produits les comprenant LU81879A1 (fr)

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 (1)

Publication Number	Publication Date
LU81879A1 true LU81879A1 (fr)	1980-04-22

Family

ID=25501865

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU81879A LU81879A1 (fr)	1978-11-09	1979-11-09	Copolyesters de p-oxybenzoyle et produits les comprenant

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
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
FI65790C (fi)	1984-07-10
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

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BR0315525B1 (pt)	2014-02-11	Composição de resina transportada por água de secagem a ar, método para produzir uma composição de resina trasportada por água de secagem a ar e uso de um polímero dentrítico de secagem a ar anfifílico
US4219629A (en)	1980-08-26	P-Oxybenzoyl copolyesters comprising thiodiphenol components and having improved flexibility and solubility in organic solvents
FR2538403A1 (fr)	1984-06-29	Procede pour la production de polyesters aromatiques
EP0015856B1 (de)	1982-11-24	Aromatische thermotrope Copolyester und Verfahren zu ihrer Herstellung
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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
FR2526029A1 (fr)	1983-11-04	Polyester dont le constituant monomere alcool polyatomique est au moins partiellement de 1,2 butanediol
US5464884A (en)	1995-11-07	Coating process and curable compositions
LU82796A1 (fr)	1981-06-04	Composition polymere thermoplastique apte au faconnage,contenant un acetal cyclique en tant qu'agent de nucleation
FR2483937A1 (fr)	1981-12-11	Composition lubrifiee d'un copolymere de polyesters aromatiques
WO2016203136A1 (fr)	2016-12-22	Resine polyester hydroxylee et/ou carboxylee a haut extrait sec et haut pouvoir couvrant pour revetement de feuille metallique
KR850000616B1 (ko)	1985-05-01	옥시벤조일 코폴리 에스테르류의 제조방법
BE560981A (de)
EP0024767B1 (de)	1982-12-01	Chlorbromierte Dicarbonsäuren, Verfahren zu ihrer Herstellung und ihre Verwendung als Feuerschutzzusätze für synthetische Materialien
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BE582626A (de)	1960-01-04
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FR3117493A1 (fr)	2022-06-17	Résines phtalonitriles spécifiques pour applications à hautes températures et procédés de préparation de celles-ci
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EP1285016A2 (de)	2003-02-26	Polyesterpolymere mit hohem molekularen gewicht, verfahren zu ihrer herstellung und verwendung
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FR2786496A1 (fr)	2000-06-02	Procede de fabrication de polyester
BE650793A (de)	1964-11-16