GB845560A - Improvements in or relating to polyamide resins - Google Patents
Improvements in or relating to polyamide resinsInfo
- Publication number
- GB845560A GB845560A GB5109/59A GB510959A GB845560A GB 845560 A GB845560 A GB 845560A GB 5109/59 A GB5109/59 A GB 5109/59A GB 510959 A GB510959 A GB 510959A GB 845560 A GB845560 A GB 845560A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acids
- specified
- carbon atoms
- fatty acid
- alkylene
- 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
- 229920006122 polyamide resin Polymers 0.000 title abstract 2
- 239000002253 acid Substances 0.000 abstract 4
- 150000007513 acids Chemical class 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 3
- 229930195729 fatty acid Natural products 0.000 abstract 3
- 239000000194 fatty acid Substances 0.000 abstract 3
- 150000004665 fatty acids Chemical class 0.000 abstract 3
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 abstract 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 125000005263 alkylenediamine group Chemical group 0.000 abstract 2
- 239000001273 butane Substances 0.000 abstract 2
- 238000001035 drying Methods 0.000 abstract 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 abstract 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 abstract 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 abstract 2
- 229920001281 polyalkylene Polymers 0.000 abstract 2
- 229920000768 polyamine Polymers 0.000 abstract 2
- 238000006116 polymerization reaction Methods 0.000 abstract 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 abstract 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical class C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 abstract 1
- 244000020518 Carthamus tinctorius Species 0.000 abstract 1
- 235000003255 Carthamus tinctorius Nutrition 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 1
- 244000068988 Glycine max Species 0.000 abstract 1
- 235000010469 Glycine max Nutrition 0.000 abstract 1
- 244000020551 Helianthus annuus Species 0.000 abstract 1
- 235000003222 Helianthus annuus Nutrition 0.000 abstract 1
- 240000006240 Linum usitatissimum Species 0.000 abstract 1
- 235000004431 Linum usitatissimum Nutrition 0.000 abstract 1
- 235000010678 Paulownia tomentosa Nutrition 0.000 abstract 1
- 240000002834 Paulownia tomentosa Species 0.000 abstract 1
- 235000004347 Perilla Nutrition 0.000 abstract 1
- 244000124853 Perilla frutescens Species 0.000 abstract 1
- 240000008042 Zea mays Species 0.000 abstract 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 abstract 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 abstract 1
- 150000001279 adipic acids Chemical class 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 239000004359 castor oil Substances 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 235000005822 corn Nutrition 0.000 abstract 1
- 235000012343 cottonseed oil Nutrition 0.000 abstract 1
- 235000004426 flaxseed Nutrition 0.000 abstract 1
- 150000002311 glutaric acids Chemical class 0.000 abstract 1
- 150000002531 isophthalic acids Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- KFDIDIIKNMZLRZ-UHFFFAOYSA-N n'-propan-2-ylpropane-1,3-diamine Chemical compound CC(C)NCCCN KFDIDIIKNMZLRZ-UHFFFAOYSA-N 0.000 abstract 1
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 abstract 1
- 239000003921 oil Substances 0.000 abstract 1
- 235000019198 oils Nutrition 0.000 abstract 1
- 150000003047 pimelic acids Chemical class 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- 239000001294 propane Substances 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 150000003330 sebacic acids Chemical class 0.000 abstract 1
- 150000003442 suberic acids Chemical class 0.000 abstract 1
- 150000003504 terephthalic acids Chemical class 0.000 abstract 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 abstract 1
- -1 trimethylene tetramine Chemical compound 0.000 abstract 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 abstract 1
- 235000021122 unsaturated fatty acids Nutrition 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/26—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
- C08G69/34—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids using polymerised unsaturated fatty acids
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyamides (AREA)
Abstract
A polyamide resin comprises the reaction product of (a) a polymeric fatty acid, (b) a dibasic acid containing from 5 to 10 carbon atoms, (c) an alkylene diamine containing from 2 to 6 carbon atoms and (d) a polyalkylene polyamine containing from 3 to 5 amino groups and in which the alkylene groups contain from 2 to 3 carbon atoms. Specified polymeric fatty acids are those derived from the polymerization of drying or semi-drying oils or from the polymerization of the free acids or simple aliphatic alcohol esters of the acids of soyabean, linseed, tung, perilla, corn, oiticica, cottonseed, tall, sunflower, safflower or dehydrated castor oils. Specified dibasic acids are glutaric, adipic, pimelic, suberic, azelaic, sebacic, terephthalic and isophthalic acids. Alkylene diamines specified are ethylene and hexamethylene diamine, 1 : 3-diamino propane, 1 : 3-diamino butane, 1 : 4-diamino butane and 3-(isopropylamino-)-propylamine. Polyalkylene polyamines specified are diethylene triamine, trimethylene tetramine, tetraethylene pentamine and 3 : 31-imino-bis-propylamine. The examples describe the preparation of resins from ethylene diamine, unsaturated fatty acid monomer, polymerized fatty acid, sebacic acid and diethylene triamine, the products being soluble in a phenol-butanol mixture.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB5109/59A GB845560A (en) | 1959-02-13 | 1959-02-13 | Improvements in or relating to polyamide resins |
| LU36902D LU36902A1 (en) | 1959-02-13 | 1959-02-20 | Polyamide resin |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB36902X | 1959-02-13 | ||
| GB5109/59A GB845560A (en) | 1959-02-13 | 1959-02-13 | Improvements in or relating to polyamide resins |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB845560A true GB845560A (en) | 1960-08-24 |
Family
ID=74183552
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB5109/59A Expired GB845560A (en) | 1959-02-13 | 1959-02-13 | Improvements in or relating to polyamide resins |
Country Status (2)
| Country | Link |
|---|---|
| GB (1) | GB845560A (en) |
| LU (1) | LU36902A1 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3253940A (en) * | 1962-09-10 | 1966-05-31 | Gen Mills Inc | Polyamides of improved melting point and increased solubility for ink binders |
| US3393163A (en) * | 1962-03-08 | 1968-07-16 | Gen Mills Inc | Salts of polymeric secondary amines |
| DE3111815A1 (en) * | 1980-03-25 | 1982-02-25 | Chem-Plast S.p.A., Milano | ADHESIVE IMPROVEMENT FOR PLASTISOLE |
| GB2170813A (en) * | 1985-02-12 | 1986-08-13 | Coates Brothers Plc | Polyamide resins |
-
1959
- 1959-02-13 GB GB5109/59A patent/GB845560A/en not_active Expired
- 1959-02-20 LU LU36902D patent/LU36902A1/en unknown
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3393163A (en) * | 1962-03-08 | 1968-07-16 | Gen Mills Inc | Salts of polymeric secondary amines |
| US3253940A (en) * | 1962-09-10 | 1966-05-31 | Gen Mills Inc | Polyamides of improved melting point and increased solubility for ink binders |
| DE3111815A1 (en) * | 1980-03-25 | 1982-02-25 | Chem-Plast S.p.A., Milano | ADHESIVE IMPROVEMENT FOR PLASTISOLE |
| GB2170813A (en) * | 1985-02-12 | 1986-08-13 | Coates Brothers Plc | Polyamide resins |
| EP0194756A3 (en) * | 1985-02-12 | 1988-05-11 | Coates Brothers Plc | Polyamide resins |
Also Published As
| Publication number | Publication date |
|---|---|
| LU36902A1 (en) | 1959-04-20 |
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