GB1281752A - Unsaturated polyesteramides and their production - Google Patents

Unsaturated polyesteramides and their production

Info

Publication number
GB1281752A
GB1281752A GB2845769A GB2845769A GB1281752A GB 1281752 A GB1281752 A GB 1281752A GB 2845769 A GB2845769 A GB 2845769A GB 2845769 A GB2845769 A GB 2845769A GB 1281752 A GB1281752 A GB 1281752A
Authority
GB
United Kingdom
Prior art keywords
diol
aminoalcohol
hydroxyacid
diols
diacid
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
GB2845769A
Inventor
Devendra Jain
Isaac Goodman
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries 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
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB1307528D priority Critical patent/GB1307528A/en
Priority to GB2845769A priority patent/GB1281752A/en
Publication of GB1281752A publication Critical patent/GB1281752A/en
Expired legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H03ELECTRONIC CIRCUITRY
    • H03GCONTROL OF AMPLIFICATION
    • H03G3/00Gain control in amplifiers or frequency changers without distortion of the input signal
    • H03G3/02Manually-operated control
    • H03G3/04Manually-operated control in untuned amplifiers
    • H03G3/10Manually-operated control in untuned amplifiers having semiconductor devices
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/44Polyester-amides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/48Polymers modified by chemical after-treatment
    • HELECTRICITY
    • H03ELECTRONIC CIRCUITRY
    • H03GCONTROL OF AMPLIFICATION
    • H03G5/00Tone control or bandwidth control in amplifiers
    • H03G5/02Manually-operated control
    • H03G5/04Manually-operated control in untuned amplifiers
    • H03G5/10Manually-operated control in untuned amplifiers having semiconductor devices
    • H03G5/12Manually-operated control in untuned amplifiers having semiconductor devices incorporating negative feedback
    • HELECTRICITY
    • H03ELECTRONIC CIRCUITRY
    • H03GCONTROL OF AMPLIFICATION
    • H03G9/00Combinations of two or more types of control, e.g. gain control and tone control
    • H03G9/02Combinations of two or more types of control, e.g. gain control and tone control in untuned amplifiers
    • H03G9/12Combinations of two or more types of control, e.g. gain control and tone control in untuned amplifiers having semiconductor devices
    • H03G9/14Combinations of two or more types of control, e.g. gain control and tone control in untuned amplifiers having semiconductor devices for gain control and tone control
    • H03G9/16Combinations of two or more types of control, e.g. gain control and tone control in untuned amplifiers having semiconductor devices for gain control and tone control incorporating negative feedback

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)
  • Macromonomer-Based Addition Polymer (AREA)
  • Amplifiers (AREA)

Abstract

1281752 Unsaturated polyesteramides IMPERIAL CHEMICAL INDUSTRIES Ltd 6 Aug 1970 [5 June 1969] 28457/69 Headings C3P and C3R Hardenable polyesters having improved solvent resistance are derived from one or more diols, at least one of which contains at least one amide group in the chain between the hydroxyl groups, and one or more dicarboxylic acids; at least one of the components containing crosslinkable unsaturation. Preferred polymers are those in which at least 5 mole per cent (based on the total number of diacid and diol residues) of the diacid and/or diol units contain unsaturation and at least some of the diol residues have the Formula (II) where R<SP>1</SP>-R<SP>4</SP> are each selected from hydrogen atoms and monovalent hydrocarbon groups or R<SP>1</SP> and R<SP>2</SP> and/or R<SP>3</SP> and R<SP>4</SP> in combination represent a divalent hydrocarbon group, R<SP>5</SP> and R<SP>7</SP> are each divalent organic groups containing up to 11 atoms between the terminal valencies, a is 0 or 1, Z and Z<SP>1</SP> are each -CO.NH- or -NH.CO- or are both -NH.CO.NH- and R<SP>6</SP> is a divalent organic radical having up to 12 atoms between the valencies or a direct link, in which case Z must be -NH.CO- and Zi -CO.NH-. The polyesteramides are prepared in the normal manner from the diol corresponding to Formula (II), other diols if required, and dicarboxylic acid(s), the latter usually containing the unsaturation. The diols are the reaction products of e.g. (a) an aminoalcohol and a dicarboxylic acid, (b) a hydroxyacid and a diamine, (c) an aminoalcohol and a hydroxyacid, (d) an aminoalcohol, an aminoacid and a hydroxyacid or (e) an aminoalcohol with a carbonic acid derivative or a di-isocyanate. Polyesters in which at least 10% of the diol units have the formula corresponding to (II) and at least 5% of the diol and/or diacid units are unsaturated are claimed per se. The examples describe the use of N,N<SP>1</SP>- di(6 - hydroxycaproyl)hexamethylenediamine, N,N<SP>1</SP> - di(2 - hydroxyethyl)oxamide, N - (6- hydroxycaproyl)isopropanolamine, N,N<SP>1</SP>-di(2- hydroxypropyl)isophthalamide and N,N<SP>1</SP>-di(6- hydroxyhexyl)urea as the amide-containing diol. These are reacted with propylene glycol and maleic anhydride or fumaric acid and also, in some examples, phthalic anhydride. A freeradical inhibitor is added to prevent premature gelation. Hardenable compositions useful e.g. for making glass fibre laminates, comprise a polyesteramide according to the invention together with a vinyl monomer, e.g. styrene or 2-hydroxyethyl methacrylate, and a hardening catalyst.
GB2845769A 1969-06-05 1969-06-05 Unsaturated polyesteramides and their production Expired GB1281752A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB1307528D GB1307528A (en) 1969-06-05 1969-06-05 Gain control of electronic amplifier arrangements
GB2845769A GB1281752A (en) 1969-06-05 1969-06-05 Unsaturated polyesteramides and their production

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2845769A GB1281752A (en) 1969-06-05 1969-06-05 Unsaturated polyesteramides and their production

Publications (1)

Publication Number Publication Date
GB1281752A true GB1281752A (en) 1972-07-12

Family

ID=10275935

Family Applications (2)

Application Number Title Priority Date Filing Date
GB2845769A Expired GB1281752A (en) 1969-06-05 1969-06-05 Unsaturated polyesteramides and their production
GB1307528D Expired GB1307528A (en) 1969-06-05 1969-06-05 Gain control of electronic amplifier arrangements

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB1307528D Expired GB1307528A (en) 1969-06-05 1969-06-05 Gain control of electronic amplifier arrangements

Country Status (1)

Country Link
GB (2) GB1281752A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0042614A1 (en) * 1980-06-23 1981-12-30 Union Carbide Corporation Curable physical mixtures and composites therefrom
WO2007099397A2 (en) * 2005-06-16 2007-09-07 Dow Global Technologies Inc. Aliphatic polyester-amide compositions and a process for producing the same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0042614A1 (en) * 1980-06-23 1981-12-30 Union Carbide Corporation Curable physical mixtures and composites therefrom
WO2007099397A2 (en) * 2005-06-16 2007-09-07 Dow Global Technologies Inc. Aliphatic polyester-amide compositions and a process for producing the same
WO2007099397A3 (en) * 2005-06-16 2007-11-29 Dow Global Technologies Inc Aliphatic polyester-amide compositions and a process for producing the same
US8080617B2 (en) 2005-06-16 2011-12-20 Dow Global Technologies Llc Aliphatic polyester-amide compositions and a process for producing the same

Also Published As

Publication number Publication date
GB1307528A (en) 1973-02-21

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee