SE503559C2 - Strålningshärdbar hypergrenad polyester, förfarande för dess framställning samt dess användning - Google Patents

Strålningshärdbar hypergrenad polyester, förfarande för dess framställning samt dess användning

Info

Publication number: SE503559C2
Authority: SE; Sweden
Prior art keywords: anhydride; meth; hydroxyl groups; acrylate; polyol
Prior art date: 1994-09-08

Application number

SE9402994A

Other languages

English (en)

Swedish (sv)

Other versions

SE9402994D0 (sv

SE9402994L (sv

Inventor

Bengt Raanby

Shi Wenfang

Original Assignee

Inst Polymerutveckling Ab

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.)

1994-09-08

Filing date

1994-09-08

Publication date

1996-07-08

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=20395166&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SE503559(C2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1994-09-08 Application filed by Inst Polymerutveckling Ab filed Critical Inst Polymerutveckling Ab

1994-09-08 Priority to SE9402994A priority Critical patent/SE503559C2/sv

1994-09-08 Publication of SE9402994D0 publication Critical patent/SE9402994D0/xx

1995-09-08 Priority to EP19950931499 priority patent/EP0779908B1/en

1995-09-08 Priority to CN95194947A priority patent/CN1070878C/zh

1995-09-08 Priority to ES95931499T priority patent/ES2140704T3/es

1995-09-08 Priority to DE69513840T priority patent/DE69513840T2/de

1995-09-08 Priority to CA 2198755 priority patent/CA2198755A1/en

1995-09-08 Priority to DK95931499T priority patent/DK0779908T3/da

1995-09-08 Priority to PT95931499T priority patent/PT779908E/pt

1995-09-08 Priority to US08/793,611 priority patent/US5834118A/en

1995-09-08 Priority to RU97105770A priority patent/RU2162861C2/ru

1995-09-08 Priority to AU34893/95A priority patent/AU704344B2/en

1995-09-08 Priority to AT95931499T priority patent/ATE187467T1/de

1995-09-08 Priority to PCT/SE1995/001013 priority patent/WO1996007688A1/en

1995-09-08 Priority to JP50943696A priority patent/JP3459647B2/ja

1996-03-09 Publication of SE9402994L publication Critical patent/SE9402994L/

1996-07-08 Publication of SE503559C2 publication Critical patent/SE503559C2/sv

1997-03-07 Priority to NO19971061A priority patent/NO311300B1/no

2000-01-13 Priority to GR20000400053T priority patent/GR3032356T3/el

Links

229920006150 hyperbranched polyester Polymers 0.000 title claims abstract description 55
238000000034 method Methods 0.000 title claims abstract description 30
238000002360 preparation method Methods 0.000 title claims description 6
230000005855 radiation Effects 0.000 title claims description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 51
150000008064 anhydrides Chemical class 0.000 claims abstract description 36
229920005989 resin Polymers 0.000 claims abstract description 29
239000011347 resin Substances 0.000 claims abstract description 29
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 28
229920005862 polyol Polymers 0.000 claims abstract description 25
230000008569 process Effects 0.000 claims abstract description 25
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 22
150000003077 polyols Chemical class 0.000 claims abstract description 22
-1 aliphatic carboxylic anhydride form ester Chemical class 0.000 claims abstract description 15
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims abstract description 15
238000000576 coating method Methods 0.000 claims abstract description 13
STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 claims abstract description 9
125000003118 aryl group Chemical group 0.000 claims abstract description 9
230000009257 reactivity Effects 0.000 claims abstract description 9
ARJOQCYCJMAIFR-UHFFFAOYSA-N prop-2-enoyl prop-2-enoate Chemical compound C=CC(=O)OC(=O)C=C ARJOQCYCJMAIFR-UHFFFAOYSA-N 0.000 claims abstract description 8
238000004519 manufacturing process Methods 0.000 claims abstract description 4
239000010409 thin film Substances 0.000 claims abstract description 4
239000000853 adhesive Substances 0.000 claims abstract description 3
230000001070 adhesive effect Effects 0.000 claims abstract description 3
239000011888 foil Substances 0.000 claims abstract description 3
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims description 24
238000006243 chemical reaction Methods 0.000 claims description 16
230000003213 activating effect Effects 0.000 claims description 11
239000000126 substance Substances 0.000 claims description 11
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 10
DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical group C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 claims description 8
DCUFMVPCXCSVNP-UHFFFAOYSA-N methacrylic anhydride Chemical group CC(=C)C(=O)OC(=O)C(C)=C DCUFMVPCXCSVNP-UHFFFAOYSA-N 0.000 claims description 7
SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical group OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 claims description 7
239000000178 monomer Substances 0.000 claims description 6
RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical group C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 claims description 6
239000003054 catalyst Substances 0.000 claims description 5
239000003112 inhibitor Substances 0.000 claims description 5
239000003999 initiator Substances 0.000 claims description 5
125000002843 carboxylic acid group Chemical group 0.000 claims description 3
230000003197 catalytic effect Effects 0.000 claims description 3
230000032050 esterification Effects 0.000 claims description 3
238000005886 esterification reaction Methods 0.000 claims description 3
239000000463 material Substances 0.000 claims description 3
239000003733 fiber-reinforced composite Substances 0.000 claims description 2
238000010526 radical polymerization reaction Methods 0.000 claims description 2
150000008065 acid anhydrides Chemical class 0.000 claims 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 claims 1
125000001931 aliphatic group Chemical group 0.000 claims 1
239000011541 reaction mixture Substances 0.000 claims 1
229920000728 polyester Polymers 0.000 abstract description 19
150000002148 esters Chemical class 0.000 abstract description 4
238000009281 ultraviolet germicidal irradiation Methods 0.000 abstract description 2
239000002131 composite material Substances 0.000 abstract 1
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 45
239000000047 product Substances 0.000 description 28
230000009477 glass transition Effects 0.000 description 7
238000002329 infrared spectrum Methods 0.000 description 7
239000007788 liquid Substances 0.000 description 7
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
239000011248 coating agent Substances 0.000 description 6
239000000203 mixture Substances 0.000 description 6
239000002904 solvent Substances 0.000 description 6
239000011230 binding agent Substances 0.000 description 5
238000001723 curing Methods 0.000 description 5
239000010408 film Substances 0.000 description 5
229920000642 polymer Polymers 0.000 description 5
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
238000003848 UV Light-Curing Methods 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
238000005259 measurement Methods 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
241000284156 Clerodendrum quadriloculare Species 0.000 description 3
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
238000009826 distribution Methods 0.000 description 3
239000004645 polyester resin Substances 0.000 description 3
239000000376 reactant Substances 0.000 description 3
238000004448 titration Methods 0.000 description 3
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
238000004458 analytical method Methods 0.000 description 2
239000012298 atmosphere Substances 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
230000007423 decrease Effects 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000012467 final product Substances 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
230000004048 modification Effects 0.000 description 2
238000012986 modification Methods 0.000 description 2
229920000139 polyethylene terephthalate Polymers 0.000 description 2
239000005020 polyethylene terephthalate Substances 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 2
229920006305 unsaturated polyester Polymers 0.000 description 2
NNNLYDWXTKOQQX-UHFFFAOYSA-N 1,1-di(prop-2-enoyloxy)propyl prop-2-enoate Chemical compound C=CC(=O)OC(CC)(OC(=O)C=C)OC(=O)C=C NNNLYDWXTKOQQX-UHFFFAOYSA-N 0.000 description 1
VOBUAPTXJKMNCT-UHFFFAOYSA-N 1-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound CCCCCC(OC(=O)C=C)OC(=O)C=C VOBUAPTXJKMNCT-UHFFFAOYSA-N 0.000 description 1
238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 1
BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 1
NJNFCDQQEIAOIF-UHFFFAOYSA-N 2-(3,4-dimethoxy-2-methylsulfanylphenyl)ethanamine Chemical compound COC1=CC=C(CCN)C(SC)=C1OC NJNFCDQQEIAOIF-UHFFFAOYSA-N 0.000 description 1
IHCCLXNEEPMSIO-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 IHCCLXNEEPMSIO-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
HOSGXJWQVBHGLT-UHFFFAOYSA-N 6-hydroxy-3,4-dihydro-1h-quinolin-2-one Chemical group N1C(=O)CCC2=CC(O)=CC=C21 HOSGXJWQVBHGLT-UHFFFAOYSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
239000002253 acid Substances 0.000 description 1
238000004220 aggregation Methods 0.000 description 1
230000002776 aggregation Effects 0.000 description 1
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
238000012512 characterization method Methods 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000010276 construction Methods 0.000 description 1
239000002537 cosmetic Substances 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
WHHUWYZKGIHNPI-UHFFFAOYSA-N cyclohexa-2,4-diene-1,1,4-tricarboxylic acid Chemical compound OC(=O)C1=CCC(C(O)=O)(C(O)=O)C=C1 WHHUWYZKGIHNPI-UHFFFAOYSA-N 0.000 description 1
239000000539 dimer Substances 0.000 description 1
XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
150000002016 disaccharides Chemical class 0.000 description 1
238000004821 distillation Methods 0.000 description 1
239000003814 drug Substances 0.000 description 1
238000005265 energy consumption Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
238000013467 fragmentation Methods 0.000 description 1
238000006062 fragmentation reaction Methods 0.000 description 1
230000004927 fusion Effects 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
229920000587 hyperbranched polymer Polymers 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-M methacrylate group Chemical group C(C(=C)C)(=O)[O-] CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
150000002772 monosaccharides Chemical class 0.000 description 1
SASNBVQSOZSTPD-UHFFFAOYSA-N n-methylphenethylamine Chemical compound CNCCC1=CC=CC=C1 SASNBVQSOZSTPD-UHFFFAOYSA-N 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
150000002924 oxiranes Chemical class 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
229920001225 polyester resin Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
239000011148 porous material Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000004321 preservation Methods 0.000 description 1
238000012545 processing Methods 0.000 description 1
238000003847 radiation curing Methods 0.000 description 1
239000002994 raw material Substances 0.000 description 1
238000011160 research Methods 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000004611 spectroscopical analysis Methods 0.000 description 1
235000011150 stannous chloride Nutrition 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
238000012360 testing method Methods 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
238000002076 thermal analysis method Methods 0.000 description 1
230000000930 thermomechanical effect Effects 0.000 description 1
AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
229960005486 vaccine Drugs 0.000 description 1
238000005292 vacuum distillation Methods 0.000 description 1
239000003643 water by type Substances 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
- C08G83/00—Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
- C08G83/002—Dendritic macromolecules
- C08G83/005—Hyperbranched macromolecules
- 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
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/123—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
- C08G63/127—Acids containing aromatic rings
- 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
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/20—Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups
- 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
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/20—Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups
- C08G63/21—Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups in the presence of unsaturated monocarboxylic acids or unsaturated monohydric alcohols or reactive derivatives thereof
- 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
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/52—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
- C08G63/56—Polyesters derived from ester-forming derivatives of polycarboxylic acids or of polyhydroxy compounds other than from esters thereof
- C08G63/58—Cyclic ethers; Cyclic carbonates; Cyclic sulfites ; Cyclic orthoesters
- 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.]
- 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.]
- Y10T428/31794—Of cross-linked polyester

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Macromonomer-Based Addition Polymer (AREA)
Polyesters Or Polycarbonates (AREA)
Polymerisation Methods In General (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Manufacture Of Macromolecular Shaped Articles (AREA)
Laminated Bodies (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

SE9402994A 1994-09-08 1994-09-08 Strålningshärdbar hypergrenad polyester, förfarande för dess framställning samt dess användning SE503559C2 (sv)

Priority Applications (16)

Application Number	Priority Date	Filing Date	Title
SE9402994A SE503559C2 (sv)	1994-09-08	1994-09-08	Strålningshärdbar hypergrenad polyester, förfarande för dess framställning samt dess användning
PCT/SE1995/001013 WO1996007688A1 (en)	1994-09-08	1995-09-08	Radiation curable resins comprising hyperbranched polyesters
JP50943696A JP3459647B2 (ja)	1994-09-08	1995-09-08	超分枝状ポリエステル及びその製造方法並びにそれを含む放射線硬化性樹脂含有組成物
PT95931499T PT779908E (pt)	1994-09-08	1995-09-08	Resinas curaveis por radiacao compreendendo poliesteres hiper-ramificados
AU34893/95A AU704344B2 (en)	1994-09-08	1995-09-08	Radiation curable resins comprising hyperbranched polyesters
ES95931499T ES2140704T3 (es)	1994-09-08	1995-09-08	Resinas curables por radiacion que comprenden poliesteres hiperramificados.
DE69513840T DE69513840T2 (de)	1994-09-08	1995-09-08	Strahlungshärtbare harze aus hyperverzweigten polyestern
CA 2198755 CA2198755A1 (en)	1994-09-08	1995-09-08	Radiation curable resins comprising hyperbranched polyesters
DK95931499T DK0779908T3 (da)	1994-09-08	1995-09-08	Strålingshærdelige harpikser omfattende hyperforgrenede polyestere
EP19950931499 EP0779908B1 (en)	1994-09-08	1995-09-08	Radiation curable resins comprising hyperbranched polyesters
US08/793,611 US5834118A (en)	1994-09-08	1995-09-08	Radiation curable resins comprising hyperbranched polyesters
RU97105770A RU2162861C2 (ru)	1994-09-08	1995-09-08	Сверхразветвленный полиэфир, способ его получения и отверждаемые излучением смолы, содержащие сверхразветвленный полиэфир
CN95194947A CN1070878C (zh)	1994-09-08	1995-09-08	含高度分支聚酯的可辐射固化树脂
AT95931499T ATE187467T1 (de)	1994-09-08	1995-09-08	Strahlungshärtbare harze aus hyperverzweigten polyestern
NO19971061A NO311300B1 (no)	1994-09-08	1997-03-07	Hyperforgrenede polyestere, fremgangsmåte for fremstilling av slike, herdbare polymerer omfattende slike, og anvendelse av disse
GR20000400053T GR3032356T3 (en)	1994-09-08	2000-01-13	Radiation curable resins comprising hyperbranched polyesters

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
SE9402994A SE503559C2 (sv)	1994-09-08	1994-09-08	Strålningshärdbar hypergrenad polyester, förfarande för dess framställning samt dess användning

Publications (3)

Publication Number	Publication Date
SE9402994D0 SE9402994D0 (sv)	1994-09-08
SE9402994L SE9402994L (sv)	1996-03-09
SE503559C2 true SE503559C2 (sv)	1996-07-08

Family

ID=20395166

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE9402994A SE503559C2 (sv)	1994-09-08	1994-09-08	Strålningshärdbar hypergrenad polyester, förfarande för dess framställning samt dess användning

Country Status (16)

Country	Link
US (1)	US5834118A (da)
EP (1)	EP0779908B1 (da)
JP (1)	JP3459647B2 (da)
CN (1)	CN1070878C (da)
AT (1)	ATE187467T1 (da)
AU (1)	AU704344B2 (da)
CA (1)	CA2198755A1 (da)
DE (1)	DE69513840T2 (da)
DK (1)	DK0779908T3 (da)
ES (1)	ES2140704T3 (da)
GR (1)	GR3032356T3 (da)
NO (1)	NO311300B1 (da)
PT (1)	PT779908E (da)
RU (1)	RU2162861C2 (da)
SE (1)	SE503559C2 (da)
WO (1)	WO1996007688A1 (da)

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1994
- 1994-09-08 SE SE9402994A patent/SE503559C2/sv not_active IP Right Cessation
1995
- 1995-09-08 DE DE69513840T patent/DE69513840T2/de not_active Expired - Fee Related
- 1995-09-08 CA CA 2198755 patent/CA2198755A1/en not_active Abandoned
- 1995-09-08 WO PCT/SE1995/001013 patent/WO1996007688A1/en not_active Ceased
- 1995-09-08 US US08/793,611 patent/US5834118A/en not_active Expired - Fee Related
- 1995-09-08 DK DK95931499T patent/DK0779908T3/da active
- 1995-09-08 AU AU34893/95A patent/AU704344B2/en not_active Ceased
- 1995-09-08 CN CN95194947A patent/CN1070878C/zh not_active Expired - Fee Related
- 1995-09-08 ES ES95931499T patent/ES2140704T3/es not_active Expired - Lifetime
- 1995-09-08 PT PT95931499T patent/PT779908E/pt unknown
- 1995-09-08 EP EP19950931499 patent/EP0779908B1/en not_active Expired - Lifetime
- 1995-09-08 AT AT95931499T patent/ATE187467T1/de not_active IP Right Cessation
- 1995-09-08 RU RU97105770A patent/RU2162861C2/ru not_active IP Right Cessation
- 1995-09-08 JP JP50943696A patent/JP3459647B2/ja not_active Expired - Fee Related
1997
- 1997-03-07 NO NO19971061A patent/NO311300B1/no not_active IP Right Cessation
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Also Published As

Publication number	Publication date
DE69513840D1 (de)	2000-01-13
ATE187467T1 (de)	1999-12-15
GR3032356T3 (en)	2000-04-27
US5834118A (en)	1998-11-10
JP3459647B2 (ja)	2003-10-20
NO971061L (no)	1997-04-30
NO971061D0 (no)	1997-03-07
CA2198755A1 (en)	1996-03-14
SE9402994D0 (sv)	1994-09-08
SE9402994L (sv)	1996-03-09
EP0779908A1 (en)	1997-06-25
PT779908E (pt)	2000-05-31
CN1163626A (zh)	1997-10-29
WO1996007688A1 (en)	1996-03-14
RU2162861C2 (ru)	2001-02-10
JPH10505377A (ja)	1998-05-26
AU3489395A (en)	1996-03-27
AU704344B2 (en)	1999-04-22
NO311300B1 (no)	2001-11-12
ES2140704T3 (es)	2000-03-01
DE69513840T2 (de)	2000-07-27
CN1070878C (zh)	2001-09-12
DK0779908T3 (da)	2000-05-08
EP0779908B1 (en)	1999-12-08

Legal Events

Date	Code	Title	Description
2003-05-06	NUG	Patent has lapsed

Publication	Publication Date	Title
SE503559C2 (sv)	1996-07-08	Strålningshärdbar hypergrenad polyester, förfarande för dess framställning samt dess användning
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