CH291100A - Process for the preparation of a new synthetic polymer. - Google Patents

Process for the preparation of a new synthetic polymer.

Info

Publication number
CH291100A
CH291100A CH291100DA CH291100A CH 291100 A CH291100 A CH 291100A CH 291100D A CH291100D A CH 291100DA CH 291100 A CH291100 A CH 291100A
Authority
CH
Switzerland
Prior art keywords
preparation
synthetic polymer
acid
ethanolamino
undecanoic acid
Prior art date
Application number
Other languages
French (fr)
Inventor
Organico Societe
Original Assignee
Organico Soc
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 Organico Soc filed Critical Organico Soc
Publication of CH291100A publication Critical patent/CH291100A/en

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
    • 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
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/68Polyesters containing atoms other than carbon, hydrogen and oxygen
    • C08G63/685Polyesters containing atoms other than carbon, hydrogen and oxygen containing nitrogen
    • C08G63/6852Polyesters containing atoms other than carbon, hydrogen and oxygen containing nitrogen derived from hydroxy carboxylic acids
    • 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
    • C08G69/02Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
    • C08G69/08Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyamides (AREA)

Description

  

      Proeédé    pour la préparation d'un nouveau     polymère        synthétique.       Le brevet principal porte sur un procédé       pour    la préparation d'une nouvelle résine  synthétique, par polycondensation, à chaud,  de l'acide     N-éthanolamino-1.1-iindécandïque.     



  Le présent brevet concerne un procédé de  préparation d'une nouvelle résine d'un type       analogue,        moulable    à chaud.  



  Ce procédé est caractérisé en ce qu'un mé  lange d'acide     N-éthanolamino-11-undécanoïque     et d'acide     ll.-amino-undécanoïque    est     chauffe.     l'état fondu jusqu'à gélification.  



  Le     copolycondensat    obtenu est     insoluble     dans les solvants du     poly-undécanamide:        form-          amide,    acétamide, acide acétique, acide     mono-          chloracétique.     



  Son point de ramollissement et sa dureté  varient selon la teneur du mélange initial en  acide     N-éthanolamino-11-undécanoïque.     



  La gélification dudit mélange se produit  d'autant plus rapidement que la teneur du  mélange initial en acide     N-éthanolamino-1.1-          undécanoïque    est plus élevée. Le chauffage  (déshydratation) est effectué de préférence  sous vide poussé, du moins pour les faibles  teneurs en acide     N-éthanolamino-1.1-undéca-          noïque.     



  Pour des teneurs de 1 à     51/o,    le mélange  réactionnel passe d'abord par un état thermo  plastique,     filable,    avec un point de fusion  légèrement plus élevé que celui du     poly-undé-          eanamide    (point de fusion:

   195  C par     exem-          ple,        pour        un        pourcentage        de        2%).        Après        géli-          fieation,    la résine thermodurcissable ne fond         plus,    mais se ramollit et devient translucide à  250  C.  



  Pour un pourcentage en acide     N-éthanol-          amino-11-undécanoïque    compris entre 5 et       50        %,        le        mélange        réactionnel        passe        encore        par     un état thermoplastique, mais il devient très  difficilement     filable    à partir d'un pourcen  tage de 10 0/0.  



  La résine obtenue après gélification de  vient extrêmement dure et résistante au choc.  Elle se ramollit, en devenant translucide, entre  300 et 320  C.  



  Pour des teneurs plus élevées que 50     11/o     en acide     N-éthanolamino-11-undécanoïque,    la  gélification se produit très rapidement. Le     co-          polycondensat    devient plus élastique. Il se ra  mollit vers 300  C.



      Process for the preparation of a new synthetic polymer. The main patent relates to a process for the preparation of a novel synthetic resin, by hot polycondensation of N-ethanolamino-1.1-indecandic acid.



  The present patent relates to a process for preparing a novel resin of a similar type, hot moldable.



  This process is characterized in that a mixture of N-ethanolamino-11-undecanoic acid and 11-amino-undecanoic acid is heated. the molten state until gelation.



  The copolycondensate obtained is insoluble in the solvents of the poly-undecanamide: form-amide, acetamide, acetic acid, mono-chloroacetic acid.



  Its softening point and its hardness vary according to the content of the initial mixture of N-ethanolamino-11-undecanoic acid.



  The gelation of said mixture occurs all the more rapidly as the content of the initial mixture of N-ethanolamino-1.1-undecanoic acid is higher. The heating (dehydration) is preferably carried out under high vacuum, at least for the low contents of N-ethanolamino-1.1-undecanoic acid.



  For contents of 1 to 51 / o, the reaction mixture first passes through a thermoplastic, spinnable state, with a melting point slightly higher than that of poly-undeeanamide (melting point:

   195 C for example, for a percentage of 2%). After gelation, the thermosetting resin no longer melts, but softens and becomes translucent at 250 C.



  For a percentage of N-ethanol-amino-11-undecanoic acid of between 5 and 50%, the reaction mixture still passes through a thermoplastic state, but it becomes very difficult to spin from a percentage of 10%.



  The resin obtained after gelation becomes extremely hard and impact resistant. It softens, becoming translucent, between 300 and 320 C.



  For contents higher than 50 11 / o of N-ethanolamino-11-undecanoic acid, gelation occurs very quickly. The co-polycondensate becomes more elastic. It softens around 300 C.

 

Claims (1)

REVENDICATION: Procédé pour la préparation d'un nouveau polymère synthétique, caractérisé en ce qu'un mélange d'acide N-éthanolamino-11-undéca- noïque et d'acide 11-a-mino-undécanoïque est. chauffé à l'état fondu jusqu'à gélification. Le copolycondensat obtenu est une résine, moulable par compression à chaud, insoluble dans le formamide, l'acétamide, l'acide acé tique, l'acide monochloracétique, et se ramol lissant, en devenant translucide, entre 250 et 320 C. CLAIM: Process for the preparation of a novel synthetic polymer, characterized in that a mixture of N-ethanolamino-11-undecanoic acid and 11-a-mino-undecanoic acid is. heated in the molten state until gelling. The copolycondensate obtained is a resin, moldable by hot compression, insoluble in formamide, acetamide, acetic acid, monochloroacetic acid, and softens smoothing, becoming translucent, between 250 and 320 C.
CH291100D 1948-04-19 1949-04-19 Process for the preparation of a new synthetic polymer. CH291100A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR287880X 1948-04-19
FR293363X 1948-04-19
FR291100X 1948-04-19

Publications (1)

Publication Number Publication Date
CH291100A true CH291100A (en) 1953-05-31

Family

ID=29424128

Family Applications (1)

Application Number Title Priority Date Filing Date
CH291100D CH291100A (en) 1948-04-19 1949-04-19 Process for the preparation of a new synthetic polymer.

Country Status (2)

Country Link
CH (1) CH291100A (en)
NL (1) NL67736C (en)

Also Published As

Publication number Publication date
NL67736C (en)

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