GB1138142A - New polyamides and a process for their manufacture - Google Patents
New polyamides and a process for their manufactureInfo
- Publication number
- GB1138142A GB1138142A GB1245066A GB1245066A GB1138142A GB 1138142 A GB1138142 A GB 1138142A GB 1245066 A GB1245066 A GB 1245066A GB 1245066 A GB1245066 A GB 1245066A GB 1138142 A GB1138142 A GB 1138142A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diamine
- acid
- condensation
- fatty acid
- aliphatic
- 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
- 239000004952 Polyamide Substances 0.000 title abstract 3
- 229920002647 polyamide Polymers 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 239000000203 mixture Substances 0.000 abstract 4
- -1 aliphatic diamine Chemical class 0.000 abstract 3
- 230000005494 condensation Effects 0.000 abstract 3
- 238000009833 condensation Methods 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
- CNPURSDMOWDNOQ-UHFFFAOYSA-N 4-methoxy-7h-pyrrolo[2,3-d]pyrimidin-2-amine Chemical compound COC1=NC(N)=NC2=C1C=CN2 CNPURSDMOWDNOQ-UHFFFAOYSA-N 0.000 abstract 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 abstract 2
- 239000000178 monomer Substances 0.000 abstract 2
- DPQHRXRAZHNGRU-UHFFFAOYSA-N 2,4,4-trimethylhexane-1,6-diamine Chemical compound NCC(C)CC(C)(C)CCN DPQHRXRAZHNGRU-UHFFFAOYSA-N 0.000 abstract 1
- FZZMTSNZRBFGGU-UHFFFAOYSA-N 2-chloro-7-fluoroquinazolin-4-amine Chemical compound FC1=CC=C2C(N)=NC(Cl)=NC2=C1 FZZMTSNZRBFGGU-UHFFFAOYSA-N 0.000 abstract 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 239000000853 adhesive Substances 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000000539 dimer Substances 0.000 abstract 1
- 229920001971 elastomer Polymers 0.000 abstract 1
- 125000004494 ethyl ester group Chemical group 0.000 abstract 1
- 150000002193 fatty amides Chemical class 0.000 abstract 1
- 239000010985 leather Substances 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 150000002739 metals Chemical class 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 150000002763 monocarboxylic acids Chemical class 0.000 abstract 1
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-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
- 239000004033 plastic Substances 0.000 abstract 1
- 229920003023 plastic Polymers 0.000 abstract 1
- 239000005060 rubber Substances 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 239000013638 trimer Substances 0.000 abstract 1
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B3/00—Ohmic-resistance heating
- H05B3/10—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor
- H05B3/16—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor the conductor being mounted on an insulating base
-
- 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
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B3/00—Ohmic-resistance heating
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
1,138,142. Polyamides. SCHERING A.G. 22 March, 1966 [1 April, 1965], No. 12450/66. Heading C3R. The invention comprises polyamides derived by condensation of (A) a polymerized fatty acid or amide-forming derivative thereof containing monomer and 55-90% of dimer, and (B) a mixture of ethylene diamine and an aliphatic diamine containing a chain of 4 to 12 carbon atoms in a molar ratio between 1 and 4 to 1. The fatty acid may be saturated or mono- or polyolefinically or acetylenically unsaturated. Amide-forming derivatives specified are methyl and ethyl esters. The polymerized fatty acid may contain up to 6 parts by weight of trimer per part by weight of monomer. The aliphatic diamine may be alkyl substituted. Compounds specified include 2,2,4- and 2,4,4- trimethylhexamethylene diamine, hexamethylene diamine, nonamethylene diamine, 2,5-dimethylhexamethylene diamine and mixtures thereof. The condensation mixture may also contain an aliphatic dicarboxylic acid having a chain of 6 to 10 carbon atoms, an aromatic or arylaliphatic dicarboxylic acid and/or an additional monocarboxylic acid. The arylaliphatic acid may be alkyl substituted. Acids specified include adipic, azelaic, sebacic, terephthalic and mixtures thereof. The condensation may be at 180-250‹ C. and a reduced pressure may be applied in the latter stages. The products may be used as adhesives for metals, plastics, rubber and leather.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DESC036817 | 1965-04-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1138142A true GB1138142A (en) | 1968-12-27 |
Family
ID=7434015
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1245066A Expired GB1138142A (en) | 1965-04-01 | 1966-03-22 | New polyamides and a process for their manufacture |
Country Status (3)
Country | Link |
---|---|
CH (1) | CH465229A (en) |
GB (1) | GB1138142A (en) |
SE (1) | SE352647B (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4051087A (en) * | 1976-05-20 | 1977-09-27 | Phillips Petroleum Company | Copolyamide |
US4341671A (en) | 1979-10-23 | 1982-07-27 | Schering Ag | Polyester amide melt adhesives |
US4373085A (en) | 1980-09-03 | 1983-02-08 | Schering Aktiengesellschaft | Polyesteramide adhesives |
US4397991A (en) | 1981-04-24 | 1983-08-09 | Schering Aktiengesellschaft | Polyesteramide adhesives and sealing compounds |
-
1966
- 1966-02-04 CH CH160366A patent/CH465229A/en unknown
- 1966-03-03 SE SE281766A patent/SE352647B/xx unknown
- 1966-03-22 GB GB1245066A patent/GB1138142A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4051087A (en) * | 1976-05-20 | 1977-09-27 | Phillips Petroleum Company | Copolyamide |
US4341671A (en) | 1979-10-23 | 1982-07-27 | Schering Ag | Polyester amide melt adhesives |
US4373085A (en) | 1980-09-03 | 1983-02-08 | Schering Aktiengesellschaft | Polyesteramide adhesives |
US4397991A (en) | 1981-04-24 | 1983-08-09 | Schering Aktiengesellschaft | Polyesteramide adhesives and sealing compounds |
Also Published As
Publication number | Publication date |
---|---|
SE352647B (en) | 1973-01-08 |
CH465229A (en) | 1968-11-15 |
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