GB1003029A - Improvements in or relating to polyesteramides - Google Patents

Improvements in or relating to polyesteramides

Info

Publication number
GB1003029A
GB1003029A GB3198360A GB3198360A GB1003029A GB 1003029 A GB1003029 A GB 1003029A GB 3198360 A GB3198360 A GB 3198360A GB 3198360 A GB3198360 A GB 3198360A GB 1003029 A GB1003029 A GB 1003029A
Authority
GB
United Kingdom
Prior art keywords
fatty acids
ethylene diamine
oil
epoxy
examples
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
Application number
GB3198360A
Inventor
Alec Frank Wilson
Alec Richard Hornsey Tawn
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Coates Brothers and Co Ltd
Original Assignee
Coates Brothers and Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority to NL128830D priority Critical patent/NL128830B/xx
Priority to NL70290D priority patent/NL70290C/xx
Priority to NL269272D priority patent/NL269272A/xx
Application filed by Coates Brothers and Co Ltd filed Critical Coates Brothers and Co Ltd
Priority to GB3198360A priority patent/GB1003029A/en
Priority to DE19611445305 priority patent/DE1445305A1/en
Priority to FR870901A priority patent/FR1333725A/en
Priority to DE19611445308 priority patent/DE1445308A1/en
Priority to FR873254A priority patent/FR81308E/en
Priority to CH1076861A priority patent/CH440511A/en
Priority to BE608234A priority patent/BE608234R/en
Priority to DK367261A priority patent/DK107763C/en
Publication of GB1003029A publication Critical patent/GB1003029A/en
Expired legal-status Critical Current

Links

Classifications

    • G—PHYSICS
    • G09—EDUCATION; CRYPTOGRAPHY; DISPLAY; ADVERTISING; SEALS
    • G09F—DISPLAYING; ADVERTISING; SIGNS; LABELS OR NAME-PLATES; SEALS
    • G09F7/00—Signs, name or number plates, letters, numerals, or symbols; Panels or boards
    • G09F7/18—Means for attaching signs, plates, panels, or boards to a supporting structure
    • 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
    • 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
    • E—FIXED CONSTRUCTIONS
    • E04—BUILDING
    • E04F—FINISHING WORK ON BUILDINGS, e.g. STAIRS, FLOORS
    • E04F13/00—Coverings or linings, e.g. for walls or ceilings
    • E04F13/07—Coverings or linings, e.g. for walls or ceilings composed of covering or lining elements; Sub-structures therefor; Fastening means therefor
    • E04F13/08—Coverings or linings, e.g. for walls or ceilings composed of covering or lining elements; Sub-structures therefor; Fastening means therefor composed of a plurality of similar covering or lining elements
    • E04F13/18—Coverings or linings, e.g. for walls or ceilings composed of covering or lining elements; Sub-structures therefor; Fastening means therefor composed of a plurality of similar covering or lining elements of organic plastics with or without reinforcements or filling materials or with an outer layer of organic plastics with or without reinforcements or filling materials; plastic tiles
    • G—PHYSICS
    • G09—EDUCATION; CRYPTOGRAPHY; DISPLAY; ADVERTISING; SEALS
    • G09F—DISPLAYING; ADVERTISING; SIGNS; LABELS OR NAME-PLATES; SEALS
    • G09F7/00—Signs, name or number plates, letters, numerals, or symbols; Panels or boards
    • G09F7/18—Means for attaching signs, plates, panels, or boards to a supporting structure
    • G09F2007/1843—Frames or housings to hold signs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Architecture (AREA)
  • Polymers & Plastics (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Civil Engineering (AREA)
  • Theoretical Computer Science (AREA)
  • General Physics & Mathematics (AREA)
  • Physics & Mathematics (AREA)
  • Structural Engineering (AREA)
  • Paints Or Removers (AREA)
  • Polyamides (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A method of making a concentrated thixotropic material comprises reacting an alphaomega diprimary amine with a polymeric fatty acid under conditions promoting polyamideformation and in the presence of a suitable epoxy or hydroxy compound, the amount of polymeric fatty acid being sufficient to afford a stoichiometrical excess over the amine and epoxy or hydroxy compound. The epoxy and hydroxy compounds are defined as being (a) hydroxyl terminated polyalkylene oxides of the formula R(OR1)nOR2 and tri- or tetrahydric alcohols, one or more hydroxyl groups of which are etherified with hydroxyl terminated polyalkylene oxides of the formula (HO)pR3(OR1)n(OH)m, where R is H, alkyl or hydroxyalkyl, R1 is alkylene, R2 is H or hydroxyalkyl, R3 is the hydrocarbon residue of a tri- or tetrahydric alcohol and either p is 0, 1 or 2 and m is (3-p) when R3 is the residue of a trihydric alcohol or p is 0, 1, 2 or 3 and m is (4-p) when R3 is the residue of a tetrahydric alcohol; (b) aliphatic diols containing 4 or more carbon atoms, the hydroxyl groups being separated by 4 or more carbon atoms; (c) aliphatic monohydric alcohols; (d) partial esters of fatty acids or polymerized fatty acids or resin acids or mixtures of such acids and polyhydric alcohols, said partial esters containing free hydroxyl groups; (e) alkyd resins containing an excess of free hydroxyl groups over carboxyl groups and (f) epoxidized fatty oils or alkyl esters of epoxy fatty acids; many such compounds being exemplified. Examples (1) to (6) describe the preparation of thixotropic materials from dimerized fatty acid and: (1) ethylene diamine, the fatty acids of sunflower seed oil and polyethylene glycol; (2) ethylene diamine, the fatty acids of soya bean oil and polyethylene glycol; (3) ethylene diamine, sebacic acid, the fatty acids of soya bean oil and polyethylene glycol; (4) ethylene diamine, the fatty acids of soya bean oil and a polyoxypropylene derivative of trimethylol propane; (5) hexamethylene diamine and stearyl alcohol and (6) ethylene diamine, the fatty acids of soya bean oil and a partial ester of linseed oil with pentaerythritol. In Example (7) an alkyd derived from linseed oil-pentaerythritol and phthalic anhydride is mixed with white spirit and separately with the products of Examples (1) to (5). In Examples (8) and (9) the product of Example (6) is mixed with linseed stand oil and white spirit; the products of Examples (7) to (9) being thixotropic gels.
GB3198360A 1960-08-24 1960-09-16 Improvements in or relating to polyesteramides Expired GB1003029A (en)

Priority Applications (11)

Application Number Priority Date Filing Date Title
NL128830D NL128830B (en) 1960-09-16
NL70290D NL70290C (en) 1960-09-16
NL269272D NL269272A (en) 1960-09-16
GB3198360A GB1003029A (en) 1960-09-16 1960-09-16 Improvements in or relating to polyesteramides
DE19611445305 DE1445305A1 (en) 1960-08-24 1961-08-14 Process for making thixotropic materials
FR870901A FR1333725A (en) 1960-09-16 1961-08-17 Improvements to and relating to coating compositions
DE19611445308 DE1445308A1 (en) 1960-08-24 1961-09-14 Process for making thioxotropic materials
FR873254A FR81308E (en) 1960-09-16 1961-09-15 Improvements to and relating to coating compositions
CH1076861A CH440511A (en) 1960-08-24 1961-09-15 Process for preparing a thixotropic product
BE608234A BE608234R (en) 1960-09-16 1961-09-15 Improvements in coating compositions
DK367261A DK107763C (en) 1960-09-16 1961-09-15 Process for the preparation of a concentrated thixotropic material.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3198360A GB1003029A (en) 1960-09-16 1960-09-16 Improvements in or relating to polyesteramides

Publications (1)

Publication Number Publication Date
GB1003029A true GB1003029A (en) 1965-09-02

Family

ID=10331291

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3198360A Expired GB1003029A (en) 1960-08-24 1960-09-16 Improvements in or relating to polyesteramides

Country Status (4)

Country Link
BE (1) BE608234R (en)
DK (1) DK107763C (en)
GB (1) GB1003029A (en)
NL (3) NL128830B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0692509A3 (en) * 1994-07-11 1997-07-02 Rheox Int Pourable liquid rheological additives and the use thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH687817A5 (en) * 1994-03-25 1997-02-28 Alusuisse Lonza Services Ag body framework

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0692509A3 (en) * 1994-07-11 1997-07-02 Rheox Int Pourable liquid rheological additives and the use thereof

Also Published As

Publication number Publication date
NL70290C (en)
NL269272A (en)
NL128830B (en)
DK107763C (en) 1967-07-03
BE608234R (en) 1962-01-02

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