JP5043647B2 - 多分枝有機／無機ハイブリッドポリマー及びその製造方法 - Google Patents
多分枝有機／無機ハイブリッドポリマー及びその製造方法 Download PDFInfo
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- JP5043647B2 JP5043647B2 JP2007508292A JP2007508292A JP5043647B2 JP 5043647 B2 JP5043647 B2 JP 5043647B2 JP 2007508292 A JP2007508292 A JP 2007508292A JP 2007508292 A JP2007508292 A JP 2007508292A JP 5043647 B2 JP5043647 B2 JP 5043647B2
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- Prior art keywords
- organic
- inorganic hybrid
- hybrid polymer
- unsaturated
- compound
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- Expired - Fee Related
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- 229920000642 polymer Polymers 0.000 title claims abstract description 51
- 238000004519 manufacturing process Methods 0.000 title claims description 13
- 239000000047 product Substances 0.000 claims abstract description 38
- 150000001412 amines Chemical class 0.000 claims abstract description 14
- 150000002118 epoxides Chemical class 0.000 claims abstract description 10
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 8
- 239000002253 acid Substances 0.000 claims abstract description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
- 239000001257 hydrogen Substances 0.000 claims abstract description 7
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 6
- 125000003118 aryl group Chemical group 0.000 claims abstract description 6
- 239000007859 condensation product Substances 0.000 claims abstract description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 6
- 125000000732 arylene group Chemical group 0.000 claims abstract 3
- 238000006460 hydrolysis reaction Methods 0.000 claims description 25
- 230000007062 hydrolysis Effects 0.000 claims description 24
- 150000001875 compounds Chemical class 0.000 claims description 19
- 238000009833 condensation Methods 0.000 claims description 16
- 230000005494 condensation Effects 0.000 claims description 16
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- 229920006395 saturated elastomer Polymers 0.000 claims description 12
- 229910052710 silicon Inorganic materials 0.000 claims description 12
- 229920001169 thermoplastic Polymers 0.000 claims description 12
- 239000004416 thermosoftening plastic Substances 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 11
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 239000007788 liquid Substances 0.000 claims description 9
- 229910000077 silane Inorganic materials 0.000 claims description 9
- 239000010703 silicon Substances 0.000 claims description 9
- 238000003980 solgel method Methods 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
- 229910052796 boron Inorganic materials 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 239000001301 oxygen Substances 0.000 claims description 8
- 229910052698 phosphorus Inorganic materials 0.000 claims description 8
- 239000011574 phosphorus Substances 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 8
- 229920001187 thermosetting polymer Polymers 0.000 claims description 8
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 7
- 150000001299 aldehydes Chemical class 0.000 claims description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- 239000011593 sulfur Substances 0.000 claims description 7
- 229910052717 sulfur Inorganic materials 0.000 claims description 7
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 6
- 239000003963 antioxidant agent Substances 0.000 claims description 5
- 230000003078 antioxidant effect Effects 0.000 claims description 4
- 239000004922 lacquer Substances 0.000 claims description 4
- 125000005647 linker group Chemical group 0.000 claims description 4
- 239000006096 absorbing agent Substances 0.000 claims description 3
- 239000000853 adhesive Substances 0.000 claims description 3
- 230000001070 adhesive effect Effects 0.000 claims description 3
- 239000003431 cross linking reagent Substances 0.000 claims description 3
- 239000002516 radical scavenger Substances 0.000 claims description 3
- 238000006467 substitution reaction Methods 0.000 claims description 3
- 239000013538 functional additive Substances 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 150000001728 carbonyl compounds Chemical class 0.000 claims 1
- -1 sulphinyl Chemical group 0.000 abstract description 6
- 150000001298 alcohols Chemical class 0.000 abstract description 3
- 150000007513 acids Chemical class 0.000 abstract description 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 2
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 abstract 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical group O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000005328 phosphinyl group Chemical group [PH2](=O)* 0.000 abstract 1
- 239000000412 dendrimer Substances 0.000 description 31
- 229920000736 dendritic polymer Polymers 0.000 description 30
- 238000002474 experimental method Methods 0.000 description 21
- 229920000587 hyperbranched polymer Polymers 0.000 description 18
- 239000007795 chemical reaction product Substances 0.000 description 13
- 239000000463 material Substances 0.000 description 12
- 239000000654 additive Substances 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- 239000003381 stabilizer Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- JWUXJYZVKZKLTJ-UHFFFAOYSA-N Triacetonamine Chemical compound CC1(C)CC(=O)CC(C)(C)N1 JWUXJYZVKZKLTJ-UHFFFAOYSA-N 0.000 description 9
- 125000000524 functional group Chemical group 0.000 description 9
- 238000000576 coating method Methods 0.000 description 8
- 230000008569 process Effects 0.000 description 8
- 230000015556 catabolic process Effects 0.000 description 7
- 238000006731 degradation reaction Methods 0.000 description 7
- 238000012986 modification Methods 0.000 description 7
- 230000004048 modification Effects 0.000 description 7
- 238000012545 processing Methods 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- 229920005992 thermoplastic resin Polymers 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
- 150000003512 tertiary amines Chemical class 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 229920000333 poly(propyleneimine) Polymers 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 239000007805 chemical reaction reactant Substances 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 229920002521 macromolecule Polymers 0.000 description 4
- 150000004756 silanes Chemical class 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000005292 vacuum distillation Methods 0.000 description 4
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 3
- IAVREABSGIHHMO-UHFFFAOYSA-N 3-hydroxybenzaldehyde Chemical compound OC1=CC=CC(C=O)=C1 IAVREABSGIHHMO-UHFFFAOYSA-N 0.000 description 3
- 150000001414 amino alcohols Chemical class 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 239000007857 degradation product Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000011368 organic material Substances 0.000 description 3
- 238000010525 oxidative degradation reaction Methods 0.000 description 3
- 229920000962 poly(amidoamine) Polymers 0.000 description 3
- 239000002861 polymer material Substances 0.000 description 3
- 230000000750 progressive effect Effects 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- SFJRUJUEMVAZLM-UHFFFAOYSA-N 2-[(2-methylpropan-2-yl)oxymethyl]oxirane Chemical compound CC(C)(C)OCC1CO1 SFJRUJUEMVAZLM-UHFFFAOYSA-N 0.000 description 2
- 239000004971 Cross linker Substances 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 2
- 229910008051 Si-OH Inorganic materials 0.000 description 2
- 229910002808 Si–O–Si Inorganic materials 0.000 description 2
- 229910006358 Si—OH Inorganic materials 0.000 description 2
- 150000004703 alkoxides Chemical class 0.000 description 2
- 125000003368 amide group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 125000003636 chemical group Chemical group 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 238000007306 functionalization reaction Methods 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 150000002605 large molecules Chemical class 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920000620 organic polymer Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 229920005629 polypropylene homopolymer Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- 229920003319 Araldite® Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- 238000005684 Liebig rearrangement reaction Methods 0.000 description 1
- 229910003849 O-Si Inorganic materials 0.000 description 1
- WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical compound C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 description 1
- 229910003872 O—Si Inorganic materials 0.000 description 1
- 229910018557 Si O Inorganic materials 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 210000001787 dendrite Anatomy 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000010096 film blowing Methods 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 150000002432 hydroperoxides Chemical group 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229920000592 inorganic polymer Polymers 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 239000008204 material by function Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- SENLDUJVTGGYIH-UHFFFAOYSA-N n-(2-aminoethyl)-3-[[3-(2-aminoethylamino)-3-oxopropyl]-[2-[bis[3-(2-aminoethylamino)-3-oxopropyl]amino]ethyl]amino]propanamide Chemical compound NCCNC(=O)CCN(CCC(=O)NCCN)CCN(CCC(=O)NCCN)CCC(=O)NCCN SENLDUJVTGGYIH-UHFFFAOYSA-N 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000004597 plastic additive Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 150000003141 primary amines Chemical group 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000004224 protection Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 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
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/48—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
- C08G77/54—Nitrogen-containing linkages
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
- C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
- C08G77/388—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Silicon Polymers (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Paints Or Removers (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NO20041544 | 2004-04-15 | ||
| NO20041544A NO322777B1 (no) | 2004-04-15 | 2004-04-15 | Polyforgrenet organisk/uorganisk hybridpolymer, fremgangsmåte til dens fremstilling samt anvendelse av samme |
| PCT/NO2005/000125 WO2005100449A1 (en) | 2004-04-15 | 2005-04-15 | Polybranched, organic / inorganic hybrid polymer and method for its manufacture |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012116631A Division JP2012180528A (ja) | 2004-04-15 | 2012-05-22 | 多分枝有機／無機ハイブリッドポリマー及びその製造方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2007532748A JP2007532748A (ja) | 2007-11-15 |
| JP2007532748A5 JP2007532748A5 (https=) | 2008-05-29 |
| JP5043647B2 true JP5043647B2 (ja) | 2012-10-10 |
Family
ID=34859262
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007508292A Expired - Fee Related JP5043647B2 (ja) | 2004-04-15 | 2005-04-15 | 多分枝有機／無機ハイブリッドポリマー及びその製造方法 |
| JP2012116631A Pending JP2012180528A (ja) | 2004-04-15 | 2012-05-22 | 多分枝有機／無機ハイブリッドポリマー及びその製造方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012116631A Pending JP2012180528A (ja) | 2004-04-15 | 2012-05-22 | 多分枝有機／無機ハイブリッドポリマー及びその製造方法 |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US7960492B2 (https=) |
| EP (1) | EP1740643B1 (https=) |
| JP (2) | JP5043647B2 (https=) |
| KR (1) | KR101187691B1 (https=) |
| CN (1) | CN1976978B (https=) |
| AT (1) | ATE505505T1 (https=) |
| AU (1) | AU2005233483B2 (https=) |
| CA (1) | CA2563108C (https=) |
| DE (1) | DE602005027448D1 (https=) |
| DK (1) | DK1740643T3 (https=) |
| ES (1) | ES2363125T3 (https=) |
| NO (1) | NO322777B1 (https=) |
| PL (1) | PL1740643T3 (https=) |
| WO (1) | WO2005100449A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012180528A (ja) * | 2004-04-15 | 2012-09-20 | Sinvent As | 多分枝有機／無機ハイブリッドポリマー及びその製造方法 |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NO322911B1 (no) * | 2002-10-16 | 2006-12-18 | Sinvent As | Herder for herding av epoksyharpikser samt gjenstand fremstilt av epoksiharpiks og slik herder |
| NO346733B1 (en) | 2019-06-28 | 2022-12-05 | Klingelberg Products As | Flame retardant, method for its preparation and article comprising same |
| NO346598B1 (en) | 2020-12-23 | 2022-10-24 | Klingelberg Products As | Method for the preparation of amidines and amide manufactured by the method |
| CN115850910B (zh) * | 2022-11-11 | 2024-12-27 | 中南民族大学 | 一种生物基超支化聚合物环氧树脂及其制备方法、应用 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4772716A (en) * | 1986-07-14 | 1988-09-20 | Ciba-Geigy Corporation | Oxazolidines containing silane groups |
| EP0486469B2 (en) * | 1986-10-03 | 2000-06-21 | PPG Industries Ohio, Inc. | Organic-inorganic hybrid polymer |
| IT1230062B (it) * | 1989-04-18 | 1991-09-27 | Enichem Sintesi | Nuovi silani contenenti almeno due gruppi oxazolidinici, loro preparazione ed impiego. |
| IT1229257B (it) * | 1989-05-11 | 1991-07-26 | Enichem Sintesi | Composti silicio organici contenenti un gruppo oxazolidinico |
| JPH0873594A (ja) * | 1994-09-08 | 1996-03-19 | Yokohama Rubber Co Ltd:The | オキサゾリジン環を有するオルガノポリシロキサンおよびその組成物 |
| JPH08283580A (ja) * | 1995-04-17 | 1996-10-29 | Yokohama Rubber Co Ltd:The | オキサゾリジン環を有するシリコーンおよびこれを含有するウレタン樹脂組成物 |
| DE19822721A1 (de) * | 1997-12-23 | 1999-07-01 | Fraunhofer Ges Forschung | Filmbildendes gezielt wiederablösbares Material |
| US5997954A (en) * | 1998-07-15 | 1999-12-07 | Dow Corning Corporation | Method of rendering substrates water repellent using hyperbranched polymers containing silicon atoms |
| DE19853971B4 (de) * | 1998-11-23 | 2011-06-16 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Anorganisch/organische Polysiloxanhybridpolymere und ihre Verwendung |
| NO319405B1 (no) | 2000-07-05 | 2005-08-08 | Sintef | Organisk basert lakk eller gel-coat, fremgangsmate til fremstilling samt anvendelse av samme |
| NO322777B1 (no) * | 2004-04-15 | 2006-12-11 | Sinvent As | Polyforgrenet organisk/uorganisk hybridpolymer, fremgangsmåte til dens fremstilling samt anvendelse av samme |
-
2004
- 2004-04-15 NO NO20041544A patent/NO322777B1/no unknown
-
2005
- 2005-04-15 EP EP05737639A patent/EP1740643B1/en not_active Expired - Lifetime
- 2005-04-15 DE DE602005027448T patent/DE602005027448D1/de not_active Expired - Lifetime
- 2005-04-15 US US11/578,471 patent/US7960492B2/en active Active
- 2005-04-15 AT AT05737639T patent/ATE505505T1/de active
- 2005-04-15 AU AU2005233483A patent/AU2005233483B2/en not_active Ceased
- 2005-04-15 ES ES05737639T patent/ES2363125T3/es not_active Expired - Lifetime
- 2005-04-15 DK DK05737639.4T patent/DK1740643T3/da active
- 2005-04-15 KR KR1020067023938A patent/KR101187691B1/ko not_active Expired - Fee Related
- 2005-04-15 CN CN2005800177481A patent/CN1976978B/zh not_active Expired - Fee Related
- 2005-04-15 JP JP2007508292A patent/JP5043647B2/ja not_active Expired - Fee Related
- 2005-04-15 CA CA2563108A patent/CA2563108C/en not_active Expired - Lifetime
- 2005-04-15 WO PCT/NO2005/000125 patent/WO2005100449A1/en not_active Ceased
- 2005-04-15 PL PL05737639T patent/PL1740643T3/pl unknown
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2012
- 2012-05-22 JP JP2012116631A patent/JP2012180528A/ja active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012180528A (ja) * | 2004-04-15 | 2012-09-20 | Sinvent As | 多分枝有機／無機ハイブリッドポリマー及びその製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1740643B1 (en) | 2011-04-13 |
| US20080039607A1 (en) | 2008-02-14 |
| NO20041544D0 (no) | 2004-04-15 |
| EP1740643A1 (en) | 2007-01-10 |
| JP2007532748A (ja) | 2007-11-15 |
| NO20041544L (no) | 2005-10-17 |
| AU2005233483B2 (en) | 2011-02-03 |
| CN1976978A (zh) | 2007-06-06 |
| KR20070027548A (ko) | 2007-03-09 |
| DK1740643T3 (da) | 2011-07-18 |
| ATE505505T1 (de) | 2011-04-15 |
| ES2363125T3 (es) | 2011-07-21 |
| JP2012180528A (ja) | 2012-09-20 |
| PL1740643T3 (pl) | 2011-09-30 |
| DE602005027448D1 (de) | 2011-05-26 |
| NO322777B1 (no) | 2006-12-11 |
| CA2563108A1 (en) | 2005-10-27 |
| CN1976978B (zh) | 2011-04-20 |
| US7960492B2 (en) | 2011-06-14 |
| CA2563108C (en) | 2013-08-06 |
| WO2005100449A1 (en) | 2005-10-27 |
| KR101187691B1 (ko) | 2012-10-08 |
| AU2005233483A1 (en) | 2005-10-27 |
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