GB718822A - Synthetic polyisocyanate polymers and methods for their preparation - Google Patents
Synthetic polyisocyanate polymers and methods for their preparationInfo
- Publication number
- GB718822A GB718822A GB20367/51A GB2036751A GB718822A GB 718822 A GB718822 A GB 718822A GB 20367/51 A GB20367/51 A GB 20367/51A GB 2036751 A GB2036751 A GB 2036751A GB 718822 A GB718822 A GB 718822A
- Authority
- GB
- United Kingdom
- Prior art keywords
- adduct
- parts
- diisocyanate
- examples
- rubber
- 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
- 229920001228 polyisocyanate Polymers 0.000 title abstract 4
- 239000005056 polyisocyanate Substances 0.000 title abstract 4
- 229920000642 polymer Polymers 0.000 title abstract 4
- 229920001971 elastomer Polymers 0.000 abstract 6
- 239000005060 rubber Substances 0.000 abstract 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical class OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical class CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract 3
- 229920000728 polyester Polymers 0.000 abstract 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 abstract 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical class OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 abstract 2
- 238000004132 cross linking Methods 0.000 abstract 2
- 125000005442 diisocyanate group Chemical group 0.000 abstract 2
- 239000000806 elastomer Substances 0.000 abstract 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 239000012948 isocyanate Substances 0.000 abstract 2
- 150000002513 isocyanates Chemical class 0.000 abstract 2
- 239000000126 substance Substances 0.000 abstract 2
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 abstract 2
- ZXHZWRZAWJVPIC-UHFFFAOYSA-N 1,2-diisocyanatonaphthalene Chemical compound C1=CC=CC2=C(N=C=O)C(N=C=O)=CC=C21 ZXHZWRZAWJVPIC-UHFFFAOYSA-N 0.000 abstract 1
- LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 abstract 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 abstract 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 235000011037 adipic acid Nutrition 0.000 abstract 1
- 239000001361 adipic acid Substances 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 150000001414 amino alcohols Chemical class 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- MIHINWMALJZIBX-UHFFFAOYSA-N cyclohexa-2,4-dien-1-ol Chemical compound OC1CC=CC=C1 MIHINWMALJZIBX-UHFFFAOYSA-N 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 150000003949 imides Chemical class 0.000 abstract 1
- 150000003951 lactams Chemical class 0.000 abstract 1
- 229920000768 polyamine Polymers 0.000 abstract 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 abstract 1
- 150000003336 secondary aromatic amines Chemical class 0.000 abstract 1
- 229960002317 succinimide Drugs 0.000 abstract 1
- 150000005846 sugar alcohols Polymers 0.000 abstract 1
- 150000003509 tertiary alcohols Chemical class 0.000 abstract 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
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/80—Masked polyisocyanates
- C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2380/00—Tyres
-
- 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
- C08G2390/00—Containers
-
- 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
- C08G2410/00—Soles
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US718822XA | 1950-11-01 | 1950-11-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB718822A true GB718822A (en) | 1954-11-24 |
Family
ID=22104196
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB20367/51A Expired GB718822A (en) | 1950-11-01 | 1951-08-29 | Synthetic polyisocyanate polymers and methods for their preparation |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE506816A (enrdf_load_stackoverflow) |
| FR (1) | FR1043008A (enrdf_load_stackoverflow) |
| GB (1) | GB718822A (enrdf_load_stackoverflow) |
| LU (1) | LU30715A1 (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3375224A (en) * | 1964-01-10 | 1968-03-26 | Upjohn Co | Polyurethane impregnating and bonding resin |
| WO2008033348A1 (en) * | 2006-09-14 | 2008-03-20 | Bayer Materialscience Llc | New liquid diisocyanates prepared via modification with 1,3-dicarbonyl compounds |
| US20120302693A1 (en) * | 2011-05-23 | 2012-11-29 | E I Du Pont De Nemours And Company | Fluorine containing graft copolymer coating composition |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE959227C (de) * | 1952-12-10 | 1957-02-28 | Bayer Ag | Verfahren zur Herstellung eines Polyesteramids |
| DE3046409A1 (de) | 1980-12-10 | 1982-07-15 | Bayer Ag, 5090 Leverkusen | Beschichtungsmittel und ein verfahren zur herstellung von ueberzuegen |
| DE3312028A1 (de) * | 1983-04-02 | 1984-10-11 | Chemische Werke Hüls AG, 4370 Marl | Blockierte polysocyanate, ihre herstellung und verwendung |
| DE3739478A1 (de) * | 1987-11-21 | 1989-06-01 | Huels Chemische Werke Ag | Verfahren zur herstellung von einkomponenten-pur-einbrennlacken |
| DE3739477C2 (de) * | 1987-11-21 | 1994-04-07 | Huels Chemische Werke Ag | Verfahren zur Herstellung von monoblockierten (cyclo)-aliphatischen Diisocyanaten |
-
0
- LU LU30715D patent/LU30715A1/xx unknown
- BE BE506816D patent/BE506816A/xx unknown
-
1951
- 1951-05-21 FR FR1043008D patent/FR1043008A/fr not_active Expired
- 1951-08-29 GB GB20367/51A patent/GB718822A/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3375224A (en) * | 1964-01-10 | 1968-03-26 | Upjohn Co | Polyurethane impregnating and bonding resin |
| WO2008033348A1 (en) * | 2006-09-14 | 2008-03-20 | Bayer Materialscience Llc | New liquid diisocyanates prepared via modification with 1,3-dicarbonyl compounds |
| US20120302693A1 (en) * | 2011-05-23 | 2012-11-29 | E I Du Pont De Nemours And Company | Fluorine containing graft copolymer coating composition |
Also Published As
| Publication number | Publication date |
|---|---|
| LU30715A1 (enrdf_load_stackoverflow) | |
| FR1043008A (fr) | 1953-11-05 |
| BE506816A (enrdf_load_stackoverflow) |
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