GB1304112A - - Google Patents
Info
- Publication number
- GB1304112A GB1304112A GB416170A GB416170A GB1304112A GB 1304112 A GB1304112 A GB 1304112A GB 416170 A GB416170 A GB 416170A GB 416170 A GB416170 A GB 416170A GB 1304112 A GB1304112 A GB 1304112A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acrylate
- bicyclohept
- ethylene
- copolymer
- polyester
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 9
- 229920000728 polyester Polymers 0.000 abstract 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 6
- 150000001252 acrylic acid derivatives Chemical class 0.000 abstract 6
- 229920001577 copolymer Polymers 0.000 abstract 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 5
- 239000005977 Ethylene Substances 0.000 abstract 5
- YDKNBNOOCSNPNS-UHFFFAOYSA-N methyl 1,3-benzoxazole-2-carboxylate Chemical compound C1=CC=C2OC(C(=O)OC)=NC2=C1 YDKNBNOOCSNPNS-UHFFFAOYSA-N 0.000 abstract 4
- 239000002202 Polyethylene glycol Substances 0.000 abstract 3
- CMEXTRZFPFCOJU-UHFFFAOYSA-N bis(2-isocyanatoethyl) 7-cycloheptylcyclohept-4-ene-1,2-dicarboxylate Chemical compound N(=C=O)CCOC(=O)C1C(CC=CCC1C(=O)OCCN=C=O)C1CCCCCC1 CMEXTRZFPFCOJU-UHFFFAOYSA-N 0.000 abstract 3
- -1 dimethylsiloxane Chemical class 0.000 abstract 3
- 229920001223 polyethylene glycol Polymers 0.000 abstract 3
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 abstract 2
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 abstract 2
- JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 abstract 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 abstract 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 2
- 239000012965 benzophenone Substances 0.000 abstract 2
- 238000004132 cross linking Methods 0.000 abstract 2
- 239000003431 cross linking reagent Substances 0.000 abstract 2
- XWNVSPGTJSGNPU-UHFFFAOYSA-N ethyl 4-chloro-1h-indole-2-carboxylate Chemical compound C1=CC=C2NC(C(=O)OCC)=CC2=C1Cl XWNVSPGTJSGNPU-UHFFFAOYSA-N 0.000 abstract 2
- 239000003999 initiator Substances 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 239000000178 monomer Substances 0.000 abstract 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 2
- 150000002978 peroxides Chemical class 0.000 abstract 2
- 239000003504 photosensitizing agent Substances 0.000 abstract 2
- 229920001610 polycaprolactone Polymers 0.000 abstract 2
- 239000004632 polycaprolactone Substances 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 abstract 2
- 150000003254 radicals Chemical class 0.000 abstract 2
- SZCWBURCISJFEZ-UHFFFAOYSA-N (3-hydroxy-2,2-dimethylpropyl) 3-hydroxy-2,2-dimethylpropanoate Chemical compound OCC(C)(C)COC(=O)C(C)(C)CO SZCWBURCISJFEZ-UHFFFAOYSA-N 0.000 abstract 1
- PZJRUIBKSWBZFG-FJOGWHKWSA-N (z)-but-2-enedioic acid;ethane-1,2-diol;phthalic acid Chemical compound OCCO.OC(=O)\C=C/C(O)=O.OC(=O)C1=CC=CC=C1C(O)=O PZJRUIBKSWBZFG-FJOGWHKWSA-N 0.000 abstract 1
- 229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 abstract 1
- XQLXSGCTOLBFAK-UHFFFAOYSA-N 1-prop-2-enoyloxypentyl prop-2-enoate Chemical compound CCCCC(OC(=O)C=C)OC(=O)C=C XQLXSGCTOLBFAK-UHFFFAOYSA-N 0.000 abstract 1
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 abstract 1
- HFCUBKYHMMPGBY-UHFFFAOYSA-N 2-methoxyethyl prop-2-enoate Chemical compound COCCOC(=O)C=C HFCUBKYHMMPGBY-UHFFFAOYSA-N 0.000 abstract 1
- RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 abstract 1
- HPSGLFKWHYAKSF-UHFFFAOYSA-N 2-phenylethyl prop-2-enoate Chemical compound C=CC(=O)OCCC1=CC=CC=C1 HPSGLFKWHYAKSF-UHFFFAOYSA-N 0.000 abstract 1
- FTWUUVFSUOVZDD-UHFFFAOYSA-N 3-(2-isocyanatoethoxycarbonyl)bicyclo[2.2.1]hept-5-ene-2-carboxylic acid Chemical compound C1C2C=CC1C(C2C(=O)O)C(=O)OCCN=C=O FTWUUVFSUOVZDD-UHFFFAOYSA-N 0.000 abstract 1
- RDFQSFOGKVZWKF-UHFFFAOYSA-N 3-hydroxy-2,2-dimethylpropanoic acid Chemical compound OCC(C)(C)C(O)=O RDFQSFOGKVZWKF-UHFFFAOYSA-N 0.000 abstract 1
- SOSZGLNDFITMMF-UHFFFAOYSA-N 5-bicyclo[2.2.1]hept-2-enylmethyl bicyclo[2.2.1]hept-2-ene-5-carboxylate Chemical compound C1C(C=C2)CC2C1C(=O)OCC1C(C=C2)CC2C1 SOSZGLNDFITMMF-UHFFFAOYSA-N 0.000 abstract 1
- ZIIZNCAZYYDEAB-UHFFFAOYSA-N 5-hydroxy-2-(1-hydroxyethyl)-2,4,4-trimethylpentanoic acid Chemical compound CC(C(C)(CC(C)(C)CO)C(=O)O)O ZIIZNCAZYYDEAB-UHFFFAOYSA-N 0.000 abstract 1
- XAMCLRBWHRRBCN-UHFFFAOYSA-N 5-prop-2-enoyloxypentyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCOC(=O)C=C XAMCLRBWHRRBCN-UHFFFAOYSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 abstract 1
- OONXKOLYWJZOHG-UHFFFAOYSA-N C(C1=CC=C(C(=O)O)C=C1)(=O)O.C(C(C)O)O.C(C=C/C(=O)O)(=O)O Chemical compound C(C1=CC=C(C(=O)O)C=C1)(=O)O.C(C(C)O)O.C(C=C/C(=O)O)(=O)O OONXKOLYWJZOHG-UHFFFAOYSA-N 0.000 abstract 1
- MZFMQOZGAIVWSO-UHFFFAOYSA-N C(N)(OCC1C(CC=CCC1)C1CCCCCC1)=O.C(C)(=O)O Chemical compound C(N)(OCC1C(CC=CCC1)C1CCCCCC1)=O.C(C)(=O)O MZFMQOZGAIVWSO-UHFFFAOYSA-N 0.000 abstract 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 abstract 1
- 239000004698 Polyethylene Substances 0.000 abstract 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 abstract 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 abstract 1
- RUWBKDBLSHCCQF-UHFFFAOYSA-N [2-methyl-2-(prop-2-enoyloxymethyl)butyl] prop-2-enoate Chemical compound C=CC(=O)OCC(C)(CC)COC(=O)C=C RUWBKDBLSHCCQF-UHFFFAOYSA-N 0.000 abstract 1
- IKPLNCWDUQWFBT-UHFFFAOYSA-N [5-cycloheptyl-7-(hydroxymethyl)cyclohept-3-en-1-yl]methanol Chemical compound OCC1CC=CC(CC1CO)C1CCCCCC1 IKPLNCWDUQWFBT-UHFFFAOYSA-N 0.000 abstract 1
- 229910052786 argon Inorganic materials 0.000 abstract 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 abstract 1
- 150000008366 benzophenones Chemical class 0.000 abstract 1
- 239000004359 castor oil Substances 0.000 abstract 1
- 235000019438 castor oil Nutrition 0.000 abstract 1
- 229920002301 cellulose acetate Polymers 0.000 abstract 1
- FCSHDIVRCWTZOX-DVTGEIKXSA-N clobetasol Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H](C)[C@@](C(=O)CCl)(O)[C@@]1(C)C[C@@H]2O FCSHDIVRCWTZOX-DVTGEIKXSA-N 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004386 diacrylate group Chemical group 0.000 abstract 1
- 239000004205 dimethyl polysiloxane Substances 0.000 abstract 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 abstract 1
- 150000002009 diols Chemical class 0.000 abstract 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 abstract 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 abstract 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 abstract 1
- 239000004744 fabric Substances 0.000 abstract 1
- 239000002657 fibrous material Substances 0.000 abstract 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 abstract 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 abstract 1
- 229910052743 krypton Inorganic materials 0.000 abstract 1
- DNNSSWSSYDEUBZ-UHFFFAOYSA-N krypton atom Chemical compound [Kr] DNNSSWSSYDEUBZ-UHFFFAOYSA-N 0.000 abstract 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- LUCXVPAZUDVVBT-UHFFFAOYSA-N methyl-[3-(2-methylphenoxy)-3-phenylpropyl]azanium;chloride Chemical compound Cl.C=1C=CC=CC=1C(CCNC)OC1=CC=CC=C1C LUCXVPAZUDVVBT-UHFFFAOYSA-N 0.000 abstract 1
- 229910052754 neon Inorganic materials 0.000 abstract 1
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 abstract 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 abstract 1
- 229920000620 organic polymer Polymers 0.000 abstract 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 abstract 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 abstract 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 abstract 1
- 229920001921 poly-methyl-phenyl-siloxane Polymers 0.000 abstract 1
- 229920000573 polyethylene Polymers 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 239000004926 polymethyl methacrylate Substances 0.000 abstract 1
- 229920001451 polypropylene glycol Polymers 0.000 abstract 1
- 230000005855 radiation Effects 0.000 abstract 1
- 239000000758 substrate Substances 0.000 abstract 1
- 239000000725 suspension Substances 0.000 abstract 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 1
- 150000007964 xanthones Chemical class 0.000 abstract 1
- 229910052724 xenon Inorganic materials 0.000 abstract 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 abstract 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
- C08F2/50—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light with sensitising agents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C71/00—After-treatment of articles without altering their shape; Apparatus therefor
- B29C71/04—After-treatment of articles without altering their shape; Apparatus therefor by wave energy or particle radiation, e.g. for curing or vulcanising preformed articles
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F10/02—Ethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/01—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to 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
- C08G18/28—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
- C08G18/675—Low-molecular-weight compounds
- C08G18/676—Low-molecular-weight compounds containing the unsaturation at least partially in a non-aromatic carbocyclic ring
-
- 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
- C08G18/683—Unsaturated polyesters containing cyclic groups
- C08G18/686—Unsaturated polyesters containing cyclic groups containing cycloaliphatic 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
- 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
- C08G18/81—Unsaturated isocyanates or isothiocyanates
-
- 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
- C08G63/06—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from hydroxycarboxylic acids
-
- 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
- C08G63/54—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation the acids or hydroxy compounds containing carbocyclic rings
- C08G63/553—Acids or hydroxy compounds containing cycloaliphatic rings, e.g. Diels-Alder adducts
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/28—Treatment by wave energy or particle radiation
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M14/00—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials
- D06M14/18—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials using wave energy or particle radiation
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/44—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins
- H01B3/441—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins from alkenes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C35/00—Heating, cooling or curing, e.g. crosslinking or vulcanising; Apparatus therefor
- B29C35/02—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould
- B29C35/08—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation
- B29C35/0805—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using electromagnetic radiation
- B29C2035/0833—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using electromagnetic radiation using actinic light
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/02—Ethene
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Toxicology (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Polymerisation Methods In General (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79475269A | 1969-01-28 | 1969-01-28 | |
| US83846069A | 1969-07-02 | 1969-07-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1304112A true GB1304112A (es) | 1973-01-24 |
Family
ID=27121544
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB416170A Expired GB1304112A (es) | 1969-01-28 | 1970-01-28 |
Country Status (8)
| Country | Link |
|---|---|
| JP (1) | JPS4917871B1 (es) |
| AU (1) | AU1068270A (es) |
| BE (1) | BE744976A (es) |
| CA (1) | CA935398A (es) |
| DE (1) | DE2003132A1 (es) |
| FR (1) | FR2046111A5 (es) |
| GB (1) | GB1304112A (es) |
| NL (1) | NL7001188A (es) |
Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3992349A (en) * | 1973-12-26 | 1976-11-16 | Uop Inc. | Photodegradable polyolefin composition containing a mixture of an aryl ketone and an alkanolamine |
| US4024324A (en) * | 1975-07-17 | 1977-05-17 | Uop Inc. | Novel polyolefin composition of matter |
| US4071424A (en) * | 1971-10-18 | 1978-01-31 | Imperial Chemical Industries Limited | Photopolymerizable composition |
| US4192685A (en) | 1973-06-28 | 1980-03-11 | Teijin Limited | Photocurable unsaturated polyester resin composition and cross-linking agents |
| US4522693A (en) * | 1980-09-15 | 1985-06-11 | Basf Aktiengesellschaft | Photopolymerizable composition with acylphosphine sulfide photoinitiator and method |
| US4602076A (en) * | 1982-03-04 | 1986-07-22 | Imperial Chemical Industries Plc | Photopolymerizable compositions |
| US4767793A (en) * | 1985-11-12 | 1988-08-30 | The Goodyear Tire & Rubber Company | Method of producing a foam from a radiation-curable composition |
| US4828583A (en) * | 1987-04-02 | 1989-05-09 | Minnesota Mining And Manufacturing Company | Coated abrasive binder containing ternary photoinitiator system |
| US5066231A (en) * | 1990-02-23 | 1991-11-19 | Minnesota Mining And Manufacturing Company | Dental impression process using polycaprolactone molding composition |
| US5403188A (en) * | 1990-02-23 | 1995-04-04 | Oxman; Joel D. | Dental crowns and bridges from semi-thermoplastic molding compositions having heat-stable custom shape memory |
| US5545676A (en) * | 1987-04-02 | 1996-08-13 | Minnesota Mining And Manufacturing Company | Ternary photoinitiator system for addition polymerization |
| US5709548A (en) * | 1990-02-23 | 1998-01-20 | Minnesota Mining And Manufacturing Company | Dental crown liner composition and methods of preparing provisional applications |
| EP1209212A1 (en) * | 1999-08-27 | 2002-05-29 | Sekisui Chemical Co., Ltd. | Adhesive composition and method of bonding with the adhesive composition |
| US6696154B2 (en) | 1999-07-27 | 2004-02-24 | Pirelli Cavi E Sistemi S.P.A. | Cable, in particular for transport or distribution of electrical energy and insulating composition |
| US7297306B2 (en) | 2002-04-26 | 2007-11-20 | Albemarle Corporation | Class of amine coinitiators in photoinitiated polymerizations |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4025386C2 (de) * | 1990-08-10 | 1993-09-30 | Herberts Gmbh | Carboxyphosphanoxide und deren Verwendung als Photoinitiatoren zur Härtung von radikalisch polymerisierbaren Massen, Überzügen und Druckfarben |
| EP2403911A1 (de) | 2009-03-04 | 2012-01-11 | Basf Se | Strahlungshärtbare beschichtungsmassen, enthaltend diacrylate |
| DE102012208818A1 (de) * | 2012-05-25 | 2013-11-28 | Evonik Industries Ag | Direkte Aushärtung von Reaktionsharzen durch Plasmainduktion |
-
1970
- 1970-01-16 CA CA072277A patent/CA935398A/en not_active Expired
- 1970-01-24 DE DE19702003132 patent/DE2003132A1/de active Pending
- 1970-01-27 BE BE744976D patent/BE744976A/xx unknown
- 1970-01-27 AU AU10682/70A patent/AU1068270A/en not_active Expired
- 1970-01-28 NL NL7001188A patent/NL7001188A/xx unknown
- 1970-01-28 GB GB416170A patent/GB1304112A/en not_active Expired
- 1970-01-28 FR FR7002972A patent/FR2046111A5/fr not_active Expired
-
1972
- 1972-05-24 JP JP47050858A patent/JPS4917871B1/ja active Pending
Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4071424A (en) * | 1971-10-18 | 1978-01-31 | Imperial Chemical Industries Limited | Photopolymerizable composition |
| US4192685A (en) | 1973-06-28 | 1980-03-11 | Teijin Limited | Photocurable unsaturated polyester resin composition and cross-linking agents |
| US3992349A (en) * | 1973-12-26 | 1976-11-16 | Uop Inc. | Photodegradable polyolefin composition containing a mixture of an aryl ketone and an alkanolamine |
| US4024324A (en) * | 1975-07-17 | 1977-05-17 | Uop Inc. | Novel polyolefin composition of matter |
| US4522693A (en) * | 1980-09-15 | 1985-06-11 | Basf Aktiengesellschaft | Photopolymerizable composition with acylphosphine sulfide photoinitiator and method |
| US4602076A (en) * | 1982-03-04 | 1986-07-22 | Imperial Chemical Industries Plc | Photopolymerizable compositions |
| US4767793A (en) * | 1985-11-12 | 1988-08-30 | The Goodyear Tire & Rubber Company | Method of producing a foam from a radiation-curable composition |
| US6017660A (en) * | 1987-04-02 | 2000-01-25 | 3M Innovative Properties Company | Inks containing a ternary photoinitiator system and image graphics prepared using same |
| US5545676A (en) * | 1987-04-02 | 1996-08-13 | Minnesota Mining And Manufacturing Company | Ternary photoinitiator system for addition polymerization |
| US4828583A (en) * | 1987-04-02 | 1989-05-09 | Minnesota Mining And Manufacturing Company | Coated abrasive binder containing ternary photoinitiator system |
| US5066231A (en) * | 1990-02-23 | 1991-11-19 | Minnesota Mining And Manufacturing Company | Dental impression process using polycaprolactone molding composition |
| US5403188A (en) * | 1990-02-23 | 1995-04-04 | Oxman; Joel D. | Dental crowns and bridges from semi-thermoplastic molding compositions having heat-stable custom shape memory |
| US5415544A (en) * | 1990-02-23 | 1995-05-16 | Minnesota Mining And Manufacturing Company | Preloaded thermoplastic dental impression tray |
| US5635545A (en) * | 1990-02-23 | 1997-06-03 | Minnesota Mining And Manufacturing Company | Semi-thermoplastic molding composition having heat-stable custom shape memory |
| US5709548A (en) * | 1990-02-23 | 1998-01-20 | Minnesota Mining And Manufacturing Company | Dental crown liner composition and methods of preparing provisional applications |
| US5753781A (en) * | 1990-02-23 | 1998-05-19 | Minnesota Mining And Manufacturing Company | Blended polycaprolactone thermoplastic molding composition |
| US6696154B2 (en) | 1999-07-27 | 2004-02-24 | Pirelli Cavi E Sistemi S.P.A. | Cable, in particular for transport or distribution of electrical energy and insulating composition |
| EP1209212A1 (en) * | 1999-08-27 | 2002-05-29 | Sekisui Chemical Co., Ltd. | Adhesive composition and method of bonding with the adhesive composition |
| EP1209212A4 (en) * | 1999-08-27 | 2002-10-30 | Sekisui Chemical Co Ltd | ADHESIVE COMPOSITION AND METHOD FOR BONDING TO THIS COMPOSITION |
| US7297306B2 (en) | 2002-04-26 | 2007-11-20 | Albemarle Corporation | Class of amine coinitiators in photoinitiated polymerizations |
Also Published As
| Publication number | Publication date |
|---|---|
| CA935398A (en) | 1973-10-16 |
| FR2046111A5 (es) | 1971-03-05 |
| BE744976A (fr) | 1970-07-27 |
| JPS4917871B1 (es) | 1974-05-04 |
| DE2003132A1 (de) | 1970-07-30 |
| AU1068270A (en) | 1971-07-29 |
| NL7001188A (es) | 1970-07-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |