GB924622A - Improvements in polyesters - Google Patents

Improvements in polyesters

Info

Publication number
GB924622A
GB924622A GB16253/59A GB1625359A GB924622A GB 924622 A GB924622 A GB 924622A GB 16253/59 A GB16253/59 A GB 16253/59A GB 1625359 A GB1625359 A GB 1625359A GB 924622 A GB924622 A GB 924622A
Authority
GB
United Kingdom
Prior art keywords
mixture
polyesters
acids
acid
melt
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
GB16253/59A
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.)
3M Co
Original Assignee
Minnesota Mining and Manufacturing Co
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 Minnesota Mining and Manufacturing Co filed Critical Minnesota Mining and Manufacturing Co
Publication of GB924622A publication Critical patent/GB924622A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/16Dicarboxylic acids and dihydroxy compounds
    • C08G63/20Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/22Plastics; Metallised plastics
    • C09J7/25Plastics; Metallised plastics based on macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
    • C09J7/255Polyesters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Artificial Filaments (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A method of making a polyester comprises heating a mixture of terephthalic acid and another dicarboxylic acid whose glycol ester is stable at 230 DEG C., or of the lower alkyl esters of said acids, and an approximately stoichiometrically equivalent amount of a mixture of a polymethylene glycol of the formula HO-(CH2)n-OH where n is from 2 to 10, and an amount, not in excess of 3 mol. per cent based on the mixture of dibasic acids, of a polyhydric alcohol having at least three hydroxyl groups attached to non-tertiary carbon atoms, at a temperature sufficiently high to melt the mixture, simultaneously removing by distillation volatile products of condensation, and continuing the heating until a stage is reached where filaments formed from the melt can be cold-drawn. Specified dicarboxylic acids are isophthalic acid, sebacic acid and naphthalene dicarboxylic acid. The examples describe the preparation of polyesters in the presence of manganese acetate tetrahydrate from dimethyl terephthalate, dimethyl isophthalate, ethylene glycol and:-(1) and (4) 1:1:1-trimethylol propane; (2) 1:1:1-trimethylol ethane and (3) glycerol, the polyesters being extruded into film form and tensilized.
GB16253/59A 1958-05-12 1959-05-12 Improvements in polyesters Expired GB924622A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US1223904XA 1958-05-12 1958-05-12
US73452458A 1958-05-12 1958-05-12

Publications (1)

Publication Number Publication Date
GB924622A true GB924622A (en) 1963-04-24

Family

ID=26820466

Family Applications (1)

Application Number Title Priority Date Filing Date
GB16253/59A Expired GB924622A (en) 1958-05-12 1959-05-12 Improvements in polyesters

Country Status (2)

Country Link
FR (1) FR1223904A (en)
GB (1) GB924622A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4286011A (en) * 1978-03-30 1981-08-25 Minnesota Mining And Manufacturing Company Polyester films with improved processability and tear resistance

Also Published As

Publication number Publication date
FR1223904A (en) 1960-06-21

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