GB1592721A - Silane-terminated polycarbodiimide - Google Patents
Silane-terminated polycarbodiimide Download PDFInfo
- Publication number
- GB1592721A GB1592721A GB41869/77A GB4186977A GB1592721A GB 1592721 A GB1592721 A GB 1592721A GB 41869/77 A GB41869/77 A GB 41869/77A GB 4186977 A GB4186977 A GB 4186977A GB 1592721 A GB1592721 A GB 1592721A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polymer
- aromatic
- carbon atoms
- primer
- hydrogen
- 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
- 229920000642 polymer Polymers 0.000 claims description 27
- 238000000576 coating method Methods 0.000 claims description 21
- 125000003118 aryl group Chemical group 0.000 claims description 18
- 239000011248 coating agent Substances 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 15
- 239000001257 hydrogen Substances 0.000 claims description 15
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 239000000758 substrate Substances 0.000 claims description 11
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 10
- 150000002430 hydrocarbons Chemical class 0.000 claims description 10
- 125000001931 aliphatic group Chemical group 0.000 claims description 9
- 238000005299 abrasion Methods 0.000 claims description 8
- 229930195733 hydrocarbon Natural products 0.000 claims description 8
- 229910000077 silane Inorganic materials 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 7
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 7
- 239000004215 Carbon black (E152) Substances 0.000 claims description 6
- VPKDCDLSJZCGKE-UHFFFAOYSA-N carbodiimide group Chemical group N=C=N VPKDCDLSJZCGKE-UHFFFAOYSA-N 0.000 claims description 5
- 150000001718 carbodiimides Chemical class 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- 229920001059 synthetic polymer Polymers 0.000 claims 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 125000002924 primary amino group Chemical class [H]N([H])* 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 36
- 239000000853 adhesive Substances 0.000 description 19
- 230000001070 adhesive effect Effects 0.000 description 19
- 239000007787 solid Substances 0.000 description 18
- 238000010276 construction Methods 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- 239000012948 isocyanate Substances 0.000 description 8
- 150000002513 isocyanates Chemical class 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 229920000139 polyethylene terephthalate Polymers 0.000 description 7
- 239000005020 polyethylene terephthalate Substances 0.000 description 7
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- 125000005442 diisocyanate group Chemical group 0.000 description 5
- 239000000543 intermediate Substances 0.000 description 5
- -1 siloxanes Chemical class 0.000 description 5
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 4
- MAMVLIAIZBKNFL-UHFFFAOYSA-N CC1CCP(=O)=C1C1=CC=CC=C1 Chemical compound CC1CCP(=O)=C1C1=CC=CC=C1 MAMVLIAIZBKNFL-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 238000000746 purification Methods 0.000 description 4
- 150000004756 silanes Chemical class 0.000 description 4
- FRGPKMWIYVTFIQ-UHFFFAOYSA-N triethoxy(3-isocyanatopropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCN=C=O FRGPKMWIYVTFIQ-UHFFFAOYSA-N 0.000 description 4
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 3
- 229940093499 ethyl acetate Drugs 0.000 description 3
- 235000019439 ethyl acetate Nutrition 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229920006378 biaxially oriented polypropylene Polymers 0.000 description 2
- 239000011127 biaxially oriented polypropylene Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- SQNZJJAZBFDUTD-UHFFFAOYSA-N durene Chemical compound CC1=CC(C)=C(C)C=C1C SQNZJJAZBFDUTD-UHFFFAOYSA-N 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 150000003141 primary amines Chemical class 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- VGHSXKTVMPXHNG-UHFFFAOYSA-N 1,3-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC(N=C=O)=C1 VGHSXKTVMPXHNG-UHFFFAOYSA-N 0.000 description 1
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
- KDLIYVDINLSKGR-UHFFFAOYSA-N 1-isocyanato-4-(4-isocyanatophenoxy)benzene Chemical compound C1=CC(N=C=O)=CC=C1OC1=CC=C(N=C=O)C=C1 KDLIYVDINLSKGR-UHFFFAOYSA-N 0.000 description 1
- ULFQXMOHNAYWPP-UHFFFAOYSA-N 1-isocyanato-4-(4-isocyanatophenyl)sulfinylbenzene Chemical compound C1=CC(N=C=O)=CC=C1S(=O)C1=CC=C(N=C=O)C=C1 ULFQXMOHNAYWPP-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- 229920002799 BoPET Polymers 0.000 description 1
- IWDKNSTWZDLDGJ-UHFFFAOYSA-N CC1=P(=O)CCC1 Chemical compound CC1=P(=O)CCC1 IWDKNSTWZDLDGJ-UHFFFAOYSA-N 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- DXCPEDGVEJWXRB-UHFFFAOYSA-N N=C=O.N=C=O.CC1=CC(C)=C(C)C=C1C Chemical compound N=C=O.N=C=O.CC1=CC(C)=C(C)C=C1C DXCPEDGVEJWXRB-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- WSDQIHATCCOMLH-UHFFFAOYSA-N phenyl n-(3,5-dichlorophenyl)carbamate Chemical compound ClC1=CC(Cl)=CC(NC(=O)OC=2C=CC=CC=2)=C1 WSDQIHATCCOMLH-UHFFFAOYSA-N 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 239000013047 polymeric layer Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229920005613 synthetic organic polymer Polymers 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- 125000005628 tolylene group Chemical group 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- 239000003039 volatile agent 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
- 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
- C08G18/71—Monoisocyanates or monoisothiocyanates
- C08G18/718—Monoisocyanates or monoisothiocyanates containing silicon
-
- 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
- C08G18/02—Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only
- C08G18/025—Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only the polymeric products containing carbodiimide 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
- C08G18/28—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
- C08G18/69—Polymers of conjugated dienes
-
- 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]
- Y10T428/31511—Of epoxy ether
-
- 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]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31598—Next to silicon-containing [silicone, cement, etc.] layer
-
- 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]
- Y10T428/31652—Of asbestos
- Y10T428/31663—As siloxane, silicone or silane
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Paints Or Removers (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Polyurethanes Or Polyureas (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Laminated Bodies (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73081076A | 1976-10-08 | 1976-10-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1592721A true GB1592721A (en) | 1981-07-08 |
Family
ID=24936897
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB41869/77A Expired GB1592721A (en) | 1976-10-08 | 1977-10-07 | Silane-terminated polycarbodiimide |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4118536A (enExample) |
| JP (1) | JPS5829972B2 (enExample) |
| BR (1) | BR7706734A (enExample) |
| CA (1) | CA1099844A (enExample) |
| DE (1) | DE2745228C3 (enExample) |
| FR (1) | FR2367089A1 (enExample) |
| GB (1) | GB1592721A (enExample) |
| IT (1) | IT1091304B (enExample) |
| ZA (1) | ZA776017B (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2177710A (en) * | 1985-03-29 | 1987-01-28 | Nisshin Spinning | A thermosetting resin and a method for producing it |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2476666A1 (fr) * | 1980-02-25 | 1981-08-28 | Rhone Poulenc Ind | Nouveau procede de couplage entre un elastomere et une charge notamment a base d'un compose de la silice |
| US4396650A (en) * | 1981-05-20 | 1983-08-02 | Minnesota Mining And Manufacturing Company | Primed inorganic substrates overcoated with curable protective compositions |
| US4396681A (en) * | 1981-06-10 | 1983-08-02 | Essex Chemical Corporation | Process for coating one pot moisture curable coating composition onto non-porous substrate and article |
| US4582887A (en) * | 1984-08-30 | 1986-04-15 | Texaco Inc. | Reaction injection molded elastomers |
| US4585850A (en) * | 1984-08-30 | 1986-04-29 | Texaco Inc. | Flakeglass with sizing, amino, chloro, isocyanate agents coated directly onto the glass in RRIM elastomers |
| US4757014A (en) * | 1985-11-08 | 1988-07-12 | Minnesota Mining And Manufacturing Company | Immobilization of biologically active protein on a polymeric fibrous support |
| US4829001A (en) * | 1985-11-08 | 1989-05-09 | Minnesota Mining And Manufacturing Company | Enzymatic neutralization of hydrogen peroxide |
| GB8916739D0 (en) * | 1989-07-21 | 1989-09-06 | Minnesota Mining & Mfg | Protective layer for magnetic recording media |
| DE69110088T2 (de) * | 1990-06-01 | 1995-10-19 | Nisshin Spinning | Hitzebeständiger Klebstoff und diesen anwendendes Klebeverfahren. |
| JP3708567B2 (ja) * | 1994-07-20 | 2005-10-19 | 日清紡績株式会社 | 生物学的に活性な物質を固定するための方法 |
| KR100304475B1 (ko) * | 1996-01-18 | 2001-11-22 | 야마모토 히데키 | 방향족폴리카보디이미드및이로부터제조된필름 |
| DE69720593T2 (de) * | 1996-05-29 | 2003-11-27 | Nitto Denko Corp., Ibaraki | Aromatisches Polycarbodiimid und daraus hergestellte Folien |
| US5916675A (en) * | 1996-06-14 | 1999-06-29 | Shin-Etsu Chemical Co., Ltd. | Polycarbodiimide resin-containing adhesive and flexible printed circuit board |
| US6319311B1 (en) | 1998-04-24 | 2001-11-20 | Osi Specialties, Inc. | Powder coatings employing silyl carbamates |
| EP1780231A1 (en) | 1998-04-24 | 2007-05-02 | General Electric Company | Powder coatings or adhesives employing silanes or silane treated filters |
| US6063890A (en) * | 1998-07-01 | 2000-05-16 | Basf Corporation | Polycarbodiimide polymers and their use as adhesive intermediate layers in automotive coatings |
| JP3851749B2 (ja) * | 1999-12-16 | 2006-11-29 | 日清紡績株式会社 | 樹脂付き金属箔 |
| DE102004024204A1 (de) * | 2004-05-13 | 2005-12-08 | Basf Ag | Kunststoffe enthaltend Carbodiimid |
| DE102004024195A1 (de) * | 2004-05-13 | 2005-12-01 | Basf Ag | Carbodiimide enthaltend Silangruppen |
| DE102004024196A1 (de) * | 2004-05-13 | 2005-12-01 | Basf Ag | Carbodiimide enthaltend Harnstoffgruppen und Silangruppen |
| US7405259B2 (en) * | 2005-04-29 | 2008-07-29 | Momentive Performance Materials Inc. | Silylated polymer derived from butadiene and solvent-resistant pressure sensitive adhesive composition containing same |
| JP5409011B2 (ja) * | 2006-01-19 | 2014-02-05 | ビーエーエスエフ ソシエタス・ヨーロピア | シラン基およびカルボジイミド基を有するポリウレタン接着剤 |
| JP4719065B2 (ja) * | 2006-04-20 | 2011-07-06 | 株式会社東芝 | 未臨界度測定体系の位置決め方法及び中性子検出装置 |
| AU2009309692B2 (en) | 2008-10-29 | 2015-02-05 | Basf Se | A proppant |
| US9714378B2 (en) | 2008-10-29 | 2017-07-25 | Basf Se | Proppant |
| NL2005163C2 (nl) * | 2010-07-28 | 2012-01-31 | Stahl Int Bv | Werkwijze voor de bereiding van multifunctionele polycarbodiimides, welke gebruikt worden als vernettingsmiddel. |
| EP2460649A1 (de) * | 2010-12-02 | 2012-06-06 | Rhein Chemie Rheinau GmbH | Elastomer-Faser-Verbund, Verfahren zur Herstellung und dessen Verwendung |
| JP6505676B2 (ja) * | 2014-05-23 | 2019-04-24 | 関西ペイント株式会社 | 塗料組成物、塗装物品及び塗膜形成方法 |
| EP3985046A1 (en) * | 2020-10-15 | 2022-04-20 | Essilor International | Crosslinked gel formulation |
| WO2022178091A1 (en) * | 2021-02-18 | 2022-08-25 | Ppg Industries Ohio, Inc. | Coating compositions and methods including carbodiimides |
| CN113402963B (zh) * | 2021-07-12 | 2022-05-24 | 黎明化工研究设计院有限责任公司 | 一种聚氨酯玻璃底涂剂及其制备方法 |
| FR3125423B1 (fr) | 2021-07-23 | 2024-04-26 | Oreal | Composition cosmétique comprenant au moins un composé (poly)carbodiimide et au moins un alcoxysilane aminé |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1190176B (de) * | 1961-04-25 | 1965-04-01 | Bayer Ag | Verwendung von Carbodiimiden gemeinsam mit siliciumorganischen Verbindungen als stabilisierende Mittel in estergruppenhaltigen Polyurethanen |
| US3450562A (en) * | 1965-06-18 | 1969-06-17 | Du Pont | Cellulosic materials coated with an organic polycarbodiimide |
| BE790977A (fr) * | 1971-11-06 | 1973-05-07 | Bayer Ag | Procede de preparation de produits de poly-addition silicies |
| BE790976A (fr) * | 1971-11-06 | 1973-05-07 | Bayer Ag | Derives silyles de l'uree et leur preparation |
| US3972933A (en) * | 1974-05-28 | 1976-08-03 | Monsanto Company | Preparation of carbodiimides from ureas by dehydration |
-
1977
- 1977-08-24 CA CA285,375A patent/CA1099844A/en not_active Expired
- 1977-08-25 US US05/827,784 patent/US4118536A/en not_active Expired - Lifetime
- 1977-10-07 GB GB41869/77A patent/GB1592721A/en not_active Expired
- 1977-10-07 FR FR7730235A patent/FR2367089A1/fr active Granted
- 1977-10-07 IT IT5133677A patent/IT1091304B/it active
- 1977-10-07 ZA ZA00776017A patent/ZA776017B/xx unknown
- 1977-10-07 BR BR7706734A patent/BR7706734A/pt unknown
- 1977-10-07 DE DE2745228A patent/DE2745228C3/de not_active Expired
- 1977-10-08 JP JP52121346A patent/JPS5829972B2/ja not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2177710A (en) * | 1985-03-29 | 1987-01-28 | Nisshin Spinning | A thermosetting resin and a method for producing it |
| GB2177710B (en) * | 1985-03-29 | 1989-04-26 | Nisshin Spinning | A thermosetting resin and a method for producing it |
Also Published As
| Publication number | Publication date |
|---|---|
| ZA776017B (en) | 1978-05-30 |
| CA1099844A (en) | 1981-04-21 |
| DE2745228A1 (de) | 1978-04-13 |
| IT1091304B (it) | 1985-07-06 |
| DE2745228B2 (de) | 1979-07-19 |
| DE2745228C3 (de) | 1980-03-27 |
| US4118536A (en) | 1978-10-03 |
| JPS5347499A (en) | 1978-04-27 |
| BR7706734A (pt) | 1978-07-04 |
| FR2367089A1 (fr) | 1978-05-05 |
| FR2367089B1 (enExample) | 1983-02-18 |
| JPS5829972B2 (ja) | 1983-06-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| 732 | Registration of transactions, instruments or events in the register (sect. 32/1977) | ||
| PCNP | Patent ceased through non-payment of renewal fee |