GB848837A - Improvements in or relating to the production of synthetic elastomers - Google Patents
Improvements in or relating to the production of synthetic elastomersInfo
- Publication number
- GB848837A GB848837A GB1384457A GB1384457A GB848837A GB 848837 A GB848837 A GB 848837A GB 1384457 A GB1384457 A GB 1384457A GB 1384457 A GB1384457 A GB 1384457A GB 848837 A GB848837 A GB 848837A
- Authority
- GB
- United Kingdom
- Prior art keywords
- melting
- polyesteramide
- temperature
- polyester
- diphenyl
- 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
- 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
- C08G18/40—High-molecular-weight compounds
- C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
-
- 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
-
- 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
- C08G2250/00—Compositions for preparing crystalline polymers
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)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
In a process for the manufacture of elastomeric materials from a diisocyanate and a mixture of polyesters, polyesteramides or polyethers containing in addition to at least one component melting at a temperature of less than 160 DEG C. at least one high-melting crystalline polyester or polyesteramide which melts at a temperature not less than 160 DEG C. the diisocyanate and the other ingredients are mixed at a temperature not more than 30 DEG C. below the melting point of the high-melting polyester or polyesteramide, and thereafter the mixture is cured at a temperature at least 20 DEG C. lower than the mixing temperature. Preferably the low-melting polyester, polyesteramide or polyether has a melting point between 0 DEG C. and 60 DEG C. The mixing temperature may be above the melting point of the high-melting component. Suitable high-melting polyesters and polyesteramides are those derived from an aromatic acid, such as terephthalic, 4,41-diphenyl dicarboxylic, 4,41-diphenylethane dicarboxylic or isophthalic acid (with up to 50% of other acids) and glycols, amino alcohols and diamines. The low-melting component may be a polyether, such as those described in Specification 733,624 or a substantially linear polyester or polyesteramide preferably of molecular weight 800 to 5000, e.g. polyethylene adipate, glutarate or azelate, polydiethylene glutarate or adipate, or polypentamethylene glutarate. The proportion of high melting component may be 5 to 60% by weight. The amount of diisocyanate may be 5 to 100% in excess of that required to react with all the end groups of the polyester, polyesteramide and polyether. Diphenylmethane, naphthalene, phenylene, diphenyl, dimethyl-diphenyl, diphenylethane, toluene, dimethyl - diphenyl - methane and dibenzfuran diisocyanates are specified. Curing is usually effected at 70 DEG to 150 DEG C. Curing catalysts such as tertiary amines and fillers such as carbon black, iron oxide, glue, blanc fixe, whiting, inorganic or organic pigments and plasticizers can be added. Specification 765,745 also is referred to.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE567202D BE567202A (en) | 1957-05-01 | ||
NL108885D NL108885C (en) | 1957-05-01 | ||
GB1384457A GB848837A (en) | 1957-05-01 | 1957-05-01 | Improvements in or relating to the production of synthetic elastomers |
FR1205976D FR1205976A (en) | 1957-05-01 | 1958-04-28 | Further development in the manufacture of synthetic elastomers |
DEI14776A DE1092647B (en) | 1957-05-01 | 1958-04-30 | Process for the production of molded articles from polyurethane elastomers |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1384457A GB848837A (en) | 1957-05-01 | 1957-05-01 | Improvements in or relating to the production of synthetic elastomers |
Publications (1)
Publication Number | Publication Date |
---|---|
GB848837A true GB848837A (en) | 1960-09-21 |
Family
ID=10030360
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1384457A Expired GB848837A (en) | 1957-05-01 | 1957-05-01 | Improvements in or relating to the production of synthetic elastomers |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE567202A (en) |
DE (1) | DE1092647B (en) |
FR (1) | FR1205976A (en) |
GB (1) | GB848837A (en) |
NL (1) | NL108885C (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5129559B1 (en) * | 1972-09-05 | 1976-08-26 | ||
US4186257A (en) * | 1977-02-15 | 1980-01-29 | Bayer Aktiengesellschaft | Process for the preparation of new segmented polyurethane resins derived from block copolymers being linked together through ester and/or urethane and/or urea groups |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB765745A (en) * | 1954-01-18 | 1957-01-09 | Ici Ltd | Polyisocyanate modified polyesters and polyesteramides |
-
0
- NL NL108885D patent/NL108885C/xx active
- BE BE567202D patent/BE567202A/xx unknown
-
1957
- 1957-05-01 GB GB1384457A patent/GB848837A/en not_active Expired
-
1958
- 1958-04-28 FR FR1205976D patent/FR1205976A/en not_active Expired
- 1958-04-30 DE DEI14776A patent/DE1092647B/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5129559B1 (en) * | 1972-09-05 | 1976-08-26 | ||
US4186257A (en) * | 1977-02-15 | 1980-01-29 | Bayer Aktiengesellschaft | Process for the preparation of new segmented polyurethane resins derived from block copolymers being linked together through ester and/or urethane and/or urea groups |
US4228249A (en) * | 1977-02-15 | 1980-10-14 | Bayer Aktiengesellschaft | Segmented polyurethane resins |
Also Published As
Publication number | Publication date |
---|---|
NL108885C (en) | |
DE1092647B (en) | 1960-11-10 |
FR1205976A (en) | 1960-02-05 |
BE567202A (en) |
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