GB818157A - Improvements in linear polyesters and polyesteramides - Google Patents
Improvements in linear polyesters and polyesteramidesInfo
- Publication number
- GB818157A GB818157A GB10439/56A GB1043956A GB818157A GB 818157 A GB818157 A GB 818157A GB 10439/56 A GB10439/56 A GB 10439/56A GB 1043956 A GB1043956 A GB 1043956A GB 818157 A GB818157 A GB 818157A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- chdm
- ester
- polyesteramides
- dibutyl
- 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
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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
- C08G63/688—Polyesters containing atoms other than carbon, hydrogen and oxygen containing sulfur
- C08G63/6884—Polyesters containing atoms other than carbon, hydrogen and oxygen containing sulfur derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/6888—Polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
- C08G63/199—Acids or hydroxy compounds containing cycloaliphatic rings
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/60—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/78—Preparation processes
- C08G63/80—Solid-state polycondensation
-
- 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
- C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
- C08G64/02—Aliphatic polycarbonates
- C08G64/0208—Aliphatic polycarbonates saturated
-
- 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
- C08G69/44—Polyester-amides
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
- Polyamides (AREA)
Abstract
New linear polyesters and polyesteramides are obtained by using the compound 1 : 4-cyclohexane dimethanol (CHDM) as the glycol. The substance may be used in its cis-form or transform or as a mixture thereof. In the preparation of polyesters, the dibasic acid with which the CHDM is condensed may be orthophthalic, terephthalic, isophthalic, hexahydroorthophthalic, transhexahydroterephthalic, p : p1-sulphonyl dibenzoic, 4 : 41-diphenic, 4 : 41-benzophenone dicarboxylic, 1 : 4 - naphthalene dicarboxylic or 1 : 5-naphthalene dicarboxylic acid; also 1 : 2 - di - (p - carboxyphenoxy)ethane, 1 : 2 - di - (p-carboxyphenyl)ethane or 4 : 41-dicarboxydiphenyl ether; also oxalic, carbonic, succinic, adipic, sebacic, azelaic, alpha-ethylsuberic, alpha : alpha - diethyladipic or dimethylmalonic acid; also dicarboxydiethyl ether. Ester-forming derivatives of the acids may be used, e.g. the alkyl or aryl esters, the acid halides or the anhydrides. Glycols which may be used in addition to the CHDM are ethylene glycol, 1 : 5-pentanediol, 1 : 10-decanediol, diethylene glycol, triethylene glycol, 2 : 2-dimethyl-1 : 3-propanediol, 2 - methyl - 1 : 5 - pentanediol and 1 : 4-di-(hydroxyethyl)benzene. As a modifier, hydroxypinalic, hydroxybutyric, hydroxycaproic or p-hydroxybenzoic acid may be used. In the manufacture of polyesteramides, the CHDM is condensed with a dibasic acid, e.g. one of those specified above, and also a diamine, e.g. hexamethylene diamine, ethylene diamine, benzidine or p-xylylene-a : a 1-diamine), and/or a hydroxyamine, e.g. 3 - amino - 2 : 2 - dimethylpropanol, hydroxyethylamine, hydroxyoctamethyleneamine or p-xylylene-a -hydroxy-a 1-amine, and/or an aminoacid, e.g. p-aminoethylbenzoic acid, 6-aminocaproic acid, 6-aminohexanoic acid, 7-aminohexanoic acid or 2-methyl-6-aminohexanoic acid. Hydroxyacids may be used as modifiers. "Block" polyesteramides may be prepared by the processes of U.S.A. Specifications 2,547,113 and 2,691,006. The polyesters or polyesteramides are useful in the manufacture of fibres, films, supports for photographic emulsions and moulding compositions. In examples, polyesters are prepared from (1), (2), (7)-(20), (38), (53) CHDM and dimethyl terephthalate; (3), (21)-(36), (37), (39), (40), (41), (43), (44), (45), (54), (55), (59) and (60) CHDM, dimethyl terephthalate and sebacic acid or its dibutyl ester, succinic acid or anhydride, adipic acid, azelaic acid, isophthalic acid or its dibutyl ester, dimethylmalonic acid, hydroxypinalic acid, hexahydroterephthalic acid, the dibutyl or diethyl ester of hexahydroorthophthalic acid or a mixture of alpha-ethyl suberic acid, alpha : alpha1-diethyladipic acid and sebacic acid or its diisobutyl ester; (6) CHDM and the dibutyl ester of p : p1-sulphonyl dibenzoic acid, (4), (5), (49), (50), (51), (52), (61) and (62) CHDM, the dibutyl ester of sulphonyldibenzoic acid and sebacic acid or dibutyl sebacate, succinic anhydride or dibutyl adipate, (42) CHDM and the dimethyl ester of hexahydroterephthalic acid, (46), (47), (48) CHDM, terephthalic acid or its dimethyl ester and 2 : 2-dimethylpropylene glycol, ethylene glycol or 1 : 5-pentanediol, (56) CHDM and diethyl carbonate, (57) CHDM and succinic anhydride, (58) CHDM and dimethyl isophthalate, (63) CHDM and diethyl oxolate. In further examples polyesteramides are prepared by reacting (64) CHDM, dimethy terephthalate and hexamethylene diamine, (65) CHDM, the dibutyl ester of sulphonyl dibenzoic acid and tetramethylene diamine; (66) CHDM, dimethyl terephthalate and N : N1-bis-(hydroxyethyl)terephthalamide, (67) CHDM and a hexamethylene isophthalamide prepolymer with acid end groups. Fibres and films may be made from the above polyesters or polyesteramides and may be oriented and heat-set. In examples: (53) filaments are made by forcing a fused polyester of cyclohexanedimethanol and terephthalic acid through a spinneret and winding on a conventional package; the resulting yarn is then fed over a roller at 120 DEG C. to a winder revolving at a greater speed, thus drawing it to 3.57 times its original length, and then heated at 165 DEG C. while holding it at constant length, (54) yarn made from a polyester of cyclohexanedimethanol, terephthalic acid and succinic acid is stretched to 4.67 its original length and heat-set in a similar manner; (55) a polyester of cyclohexanedimethanol, terephthalic acid and isophthalic acid is extruded into film, stretched in mutually perpendicular directions and then heat-set.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US818157XA | 1955-12-22 | 1955-12-22 | |
US554639A US2901466A (en) | 1955-12-22 | 1955-12-22 | Linear polyesters and polyester-amides from 1,4-cyclohexanedimethanol |
US823295A US3033826A (en) | 1959-06-29 | 1959-06-29 | Linear polyesters of 1, 4-cyclohexanedimethanol and amino-carboxylic acids |
Publications (1)
Publication Number | Publication Date |
---|---|
GB818157A true GB818157A (en) | 1959-08-12 |
Family
ID=30118990
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB10439/56A Expired GB818157A (en) | 1955-12-22 | 1956-04-05 | Improvements in linear polyesters and polyesteramides |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB818157A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5880220A (en) * | 1995-01-13 | 1999-03-09 | Basf Aktiengesellschaft | Biodegradable polymers, process for the preparation thereof and the use thereof for producing biodegradable moldings |
US5889135A (en) * | 1995-02-16 | 1999-03-30 | Basf Aktiengesellschaft | Biodegradable polymers, process for producing them and their use in preparing biodegradable moldings |
US6111058A (en) * | 1995-01-13 | 2000-08-29 | Basf Aktiengesellschaft | Biodegradable polyesteramide and a process of preparing |
US6353084B1 (en) | 1995-01-13 | 2002-03-05 | Basf Aktiengesellschaft | Biodegradable polyestreramide and a process of preparing |
-
1956
- 1956-04-05 GB GB10439/56A patent/GB818157A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5880220A (en) * | 1995-01-13 | 1999-03-09 | Basf Aktiengesellschaft | Biodegradable polymers, process for the preparation thereof and the use thereof for producing biodegradable moldings |
US6111058A (en) * | 1995-01-13 | 2000-08-29 | Basf Aktiengesellschaft | Biodegradable polyesteramide and a process of preparing |
US6353084B1 (en) | 1995-01-13 | 2002-03-05 | Basf Aktiengesellschaft | Biodegradable polyestreramide and a process of preparing |
US5889135A (en) * | 1995-02-16 | 1999-03-30 | Basf Aktiengesellschaft | Biodegradable polymers, process for producing them and their use in preparing biodegradable moldings |
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