GB790083A - Improvements in or relating to hardening agents for epoxide resins - Google Patents
Improvements in or relating to hardening agents for epoxide resinsInfo
- Publication number
- GB790083A GB790083A GB3389655A GB3389655A GB790083A GB 790083 A GB790083 A GB 790083A GB 3389655 A GB3389655 A GB 3389655A GB 3389655 A GB3389655 A GB 3389655A GB 790083 A GB790083 A GB 790083A
- Authority
- GB
- United Kingdom
- Prior art keywords
- parts
- epoxide
- dissolved
- triethylenetetramine
- butanol
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/50—Amines
- C08G59/5006—Amines aliphatic
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/182—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing using pre-adducts of epoxy compounds with curing agents
- C08G59/184—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing using pre-adducts of epoxy compounds with curing agents with amines
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epoxy Resins (AREA)
Abstract
Epoxide resins having an epoxide equivalent of more than one are hardened by reacting therewith products obtained by reacting an epoxide having an epoxide equivalent of less than one with a polyamine. The hardening agent is preferably obtained by condensing dihydric phenols with epi- or dichlorhydrins in proportion ranging between 1 : 0.5 and 1 : 1 in alkaline medium and without isolating the reaction product adding the polyamine dissolved in butanol or ethylene glycol. The epoxide resins are hardened by the amine adduct by heating the mixture for an hour at 70 DEG C. or for one quarter hour at 150 DEG C. In examples: (1) 228 parts by weight of p,p1-dihydroxydiphenylpropane are dissolved in 720 parts of 5 per cent caustic soda solution and condensed at 40 DEG C. with 83 parts of epichlorhydrin. The resinous epoxide obtained is dissolved in butanol, the butanol solution washed with water and the resin freed from volatiles by distillation. 50 Parts of the condensate are dissolved in ethyleneglycol and the solution heated with 50 parts triethylenetetramine for 1 hour at 100 DEG C.; volatile components including excess amine are removed by distillation in vacuo. The hardening agent thus obtained was used to harden epoxide resins having epoxy numbers of 1.6, 3.8 and 6.1; (2) a similar amine adduct was prepared by heating 114 parts p,p1-dihydroxydiphenylpropane with 41.5 parts epichlorhydrin and reacting the product with 90 parts triethylenetetramine; (3) six butanolic solutions obtained as described in (1) were reacted respectively with 130, 100, 50, 30, and 10 parts of triethylenetetramine and products containing respectively 5.19, 4.84, 3.63, 2.73, 2.2 and 1.3 per cent nitrogen were obtained; the hardening effect of these products was found to decrease with fall of nitrogen content. Specifications 691,543 and 779,566 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEC10407A DE1006152B (en) | 1954-12-11 | 1954-12-11 | Process for curing epoxy resins |
Publications (1)
Publication Number | Publication Date |
---|---|
GB790083A true GB790083A (en) | 1958-02-05 |
Family
ID=7014752
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3389655A Expired GB790083A (en) | 1954-12-11 | 1955-11-25 | Improvements in or relating to hardening agents for epoxide resins |
Country Status (5)
Country | Link |
---|---|
CH (1) | CH344843A (en) |
DE (1) | DE1006152B (en) |
FR (1) | FR1136454A (en) |
GB (1) | GB790083A (en) |
NL (2) | NL200828A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3297608A (en) * | 1963-05-31 | 1967-01-10 | Exxon Research Engineering Co | Method for curing epoxy resins under water |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1098199B (en) * | 1958-10-10 | 1961-01-26 | Bayer Ag | Process for accelerating the hardening of epoxy resins |
NL238708A (en) * | 1959-04-29 | |||
BE596954A (en) * | 1959-11-10 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE510201A (en) * | 1949-10-25 | 1900-01-01 |
-
0
- NL NL97242D patent/NL97242C/xx active
- NL NL200828D patent/NL200828A/xx unknown
-
1954
- 1954-12-11 DE DEC10407A patent/DE1006152B/en active Pending
-
1955
- 1955-09-29 CH CH344843D patent/CH344843A/en unknown
- 1955-09-30 FR FR1136454D patent/FR1136454A/en not_active Expired
- 1955-11-25 GB GB3389655A patent/GB790083A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3297608A (en) * | 1963-05-31 | 1967-01-10 | Exxon Research Engineering Co | Method for curing epoxy resins under water |
Also Published As
Publication number | Publication date |
---|---|
NL97242C (en) | |
CH344843A (en) | 1960-02-29 |
FR1136454A (en) | 1957-05-23 |
DE1006152B (en) | 1957-04-11 |
NL200828A (en) |
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