GB1513010A - Polythiodiethanol millable gums - Google Patents
Polythiodiethanol millable gumsInfo
- Publication number
- GB1513010A GB1513010A GB49650/75A GB4965075A GB1513010A GB 1513010 A GB1513010 A GB 1513010A GB 49650/75 A GB49650/75 A GB 49650/75A GB 4965075 A GB4965075 A GB 4965075A GB 1513010 A GB1513010 A GB 1513010A
- Authority
- GB
- United Kingdom
- Prior art keywords
- units
- polythioether
- iii
- derived
- diglycidyl ether
- 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
- C08G65/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group
- C08G65/4006—(I) or (II) containing elements other than carbon, oxygen, hydrogen or halogen as leaving group (X)
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/48—Polymers modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- 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
- C08G2650/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G2650/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterized by the type of post-polymerisation functionalisation
- C08G2650/20—Cross-linking
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2312/00—Crosslinking
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Polyethers (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Compounds (AREA)
Abstract
1513010 Sulphur - containing polymers AMERICAN CYANAMID CO 3 Dec 1975 [19 Dec 1974] 49650/75 Heading C3R An elastomeric copolymer of formula is obtained by reacting a diepoxide containing radical R with the terminal -OH groups of a polythioether polyol of formula where -(-OG-)- represents randomly alternating units (i) derived from thiodiethanol and units (iv) derived from an aliphatic diol that provides unsaturation in the polymer chain in such a manner that is it possible to pass from one end of the chain to the other without traversing the allylic structure. Also in -(-OG-)- there may be units (ii) -(-OR<1>-)- and (iii) -(-OR<11>-)- derived from aliphatic and aromatic diols, respectively. The ratio of units (i) to the total of units (ii), (iii) and (iv) is greater than 1 : 1, (ii) and (iii) being optional, and the content of units (iv) is from 1 to 10 mole per cent of the total mole content of -(-OG-)-. In the polymer x is an integer such that the Mooney value of the polythioether polyol is less than 20 and n is an integer such that the Mooney value of the copolymer is higher than the Mooney value of the polythioether polyol, thus enabling the elastomer to be processed on a rubber-mill. In examples polythioether polyols are obtained by reacting thiodiethanol with 4,4<1>-isopropylidenebisphenol and 3-cyclohexene-1,1-dimethanol, with the monoallyl ether of 2-ethyl-2- (hydroxymethyl)-1,3-propane diol and 4,4<1>. isopropylidene-bisphenol, with the monoallyl ether of 2-ethyl-2-hydroxymethyl)-1,3-propane. diol and with 3 - cyclohexene - 1,1 - dimethanol; the polythioether polyols are then extended by reaction with the diglycidyl ether of 4,4<1> - isopropylidenebisphenol, with the diglycidyl ether of 1,4-butanediol, with dicyclopentadiene diepoxide and with diglycidyl ether.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US53454474A | 1974-12-19 | 1974-12-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1513010A true GB1513010A (en) | 1978-06-01 |
Family
ID=24130522
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB49650/75A Expired GB1513010A (en) | 1974-12-19 | 1975-12-03 | Polythiodiethanol millable gums |
Country Status (7)
Country | Link |
---|---|
JP (1) | JPS6039692B2 (en) |
BR (1) | BR7508288A (en) |
CA (1) | CA1054294A (en) |
DE (1) | DE2557167C2 (en) |
FR (1) | FR2295078A1 (en) |
GB (1) | GB1513010A (en) |
NL (1) | NL7514645A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0987567A1 (en) * | 1998-09-08 | 2000-03-22 | Mitsui Chemicals, Inc. | A sulfur-containing (thio)ether (co)polymer and a use thereof |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1056824B (en) * | 1956-05-19 | 1959-05-06 | Bayer Ag | Process for the production of high molecular weight plastics from polythioethers and polyisocyanates |
-
1975
- 1975-11-27 CA CA240,631A patent/CA1054294A/en not_active Expired
- 1975-12-03 GB GB49650/75A patent/GB1513010A/en not_active Expired
- 1975-12-15 BR BR7508288*A patent/BR7508288A/en unknown
- 1975-12-16 FR FR7538507A patent/FR2295078A1/en active Granted
- 1975-12-16 NL NL7514645A patent/NL7514645A/en not_active Application Discontinuation
- 1975-12-18 DE DE2557167A patent/DE2557167C2/en not_active Expired
- 1975-12-19 JP JP50150717A patent/JPS6039692B2/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0987567A1 (en) * | 1998-09-08 | 2000-03-22 | Mitsui Chemicals, Inc. | A sulfur-containing (thio)ether (co)polymer and a use thereof |
US6320020B1 (en) | 1998-09-08 | 2001-11-20 | Mitsui Chemicals, Inc. | Sulfur-containing (thio)ether (co)polymer and a use thereof |
Also Published As
Publication number | Publication date |
---|---|
DE2557167A1 (en) | 1976-06-24 |
DE2557167C2 (en) | 1985-12-19 |
FR2295078B1 (en) | 1979-03-16 |
CA1054294A (en) | 1979-05-08 |
JPS5186557A (en) | 1976-07-29 |
NL7514645A (en) | 1976-06-22 |
AU8730275A (en) | 1977-06-09 |
JPS6039692B2 (en) | 1985-09-07 |
BR7508288A (en) | 1976-08-24 |
FR2295078A1 (en) | 1976-07-16 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19921203 |