DE1595112A1 - Verfahren zur Herstellung von modifizierten Mischpolymerisaten eines alpha-Olefins und einer aethylenisch alpha,ss-ungesaettigten Monocarbonsaeure - Google Patents

Verfahren zur Herstellung von modifizierten Mischpolymerisaten eines alpha-Olefins und einer aethylenisch alpha,ss-ungesaettigten Monocarbonsaeure

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Publication number
DE1595112A1
DE1595112A1 DE1965P0036182 DEP0036182A DE1595112A1 DE 1595112 A1 DE1595112 A1 DE 1595112A1 DE 1965P0036182 DE1965P0036182 DE 1965P0036182 DE P0036182 A DEP0036182 A DE P0036182A DE 1595112 A1 DE1595112 A1 DE 1595112A1
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Prior art keywords
alpha
olefin
unsaturated monocarboxylic
ethylenically
acid groups
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Granted
Application number
DE1965P0036182
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English (en)
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DE1595112C3 (de
DE1595112B2 (de
Inventor
Rees Richard Watkin
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EIDP Inc
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EI Du Pont de Nemours and Co
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Publication of DE1595112A1 publication Critical patent/DE1595112A1/de
Publication of DE1595112B2 publication Critical patent/DE1595112B2/de
Application granted granted Critical
Publication of DE1595112C3 publication Critical patent/DE1595112C3/de
Expired legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/09Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • C08K5/098Metal salts of carboxylic acids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/1055Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
    • B32B17/10743Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer containing acrylate (co)polymers or salts thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F255/00Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/30Introducing nitrogen atoms or nitrogen-containing groups
    • C08F8/32Introducing nitrogen atoms or nitrogen-containing groups by reaction with amines
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/44Preparation of metal salts or ammonium salts
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/09Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/17Amines; Quaternary ammonium compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2800/00Copolymer characterised by the proportions of the comonomers expressed
    • C08F2800/20Copolymer characterised by the proportions of the comonomers expressed as weight or mass percentages
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • C08L23/0846Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
    • C08L23/0869Acids or derivatives thereof
    • C08L23/0876Neutralised polymers, i.e. ionomers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S260/00Chemistry of carbon compounds
    • Y10S260/31Ionic cross-link
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S273/00Amusement devices: games
    • Y10S273/22Ionomer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S36/00Boots, shoes, and leggings
    • Y10S36/02Plastic
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/91Product with molecular orientation
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/13Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1352Polymer or resin containing [i.e., natural or synthetic]
    • Y10T428/139Open-ended, self-supporting conduit, cylinder, or tube-type article
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/13Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1352Polymer or resin containing [i.e., natural or synthetic]
    • Y10T428/1397Single layer [continuous layer]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31678Of metal
    • Y10T428/31692Next to addition polymer from unsaturated monomers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/31938Polymer of monoethylenically unsaturated hydrocarbon

Description

  • Verfahren zur Herstellung von modifizierten Misohpolymerisaten einges αß-undesättigten Monocarbonsäure (Zusatz zu Patent . ... ... (Patentanmeldung P 15 20 518.2) (P 31 004) Das Hauptpatent . ... ... (Patentanmeldung P 15 20 518.2, P 31 004) betrifft ein Verfahren zur Herstellung von modifizierten Mischpolymerisaten aus α-Olefin und äthylenisch αß-ungesättigten Monocarbonsäuren, das sich dadurch kennzeichnet, dass man ein Diamin, welohes mindestens 2 Kohlenstoffatome enthält und eine Dissoziationskonstante von woniger als 1 x 10-08 aufweist, mir; einem Mischpolymerisat aus einem a-Olerin, das die allgemei. ne. Formel RCH=CH2 hat, worin R Wasserstoff oder Alkyl mit 1 bis 8 kohlenstoffatomen ist, wobei der Olefingehalt des Mischpolymerisates mindestens 50 Mol% beträgt, bezogen aur das Misohpolymerisat, und einer äthylenisch α,ß-ungesättigten Monocarbonsäure mit 3 bis 8 Kohlenstoffatomen, wobeider Säuremonomergehalt des Mishcpolymerisates zwischen 0,2 und 25 Molfi liegt, bezogen auf das Mischpolymerisat, umsetzt, wobei in dem Mischpolymerisat mindestens teilweise die Säure in der ionisierten Form, -COO-vorliegt und die Menge des Diamins ausreicht, um mindestens 10 % der Säuregruppen des Mischpolymerisates zu neutralisieren.
  • Nach dem Hauptpatent . ... ... (Patentanmeldung P 31 00@ ##/39c) kann die Vernetzung durehgefUhrt werden, indem man das Caroonsäuregruppen enthaltende Misohpolymerisat mit der Diamin-Verbindung schmelzmischt oder das Diamin direkt oder in gelöster Form einer Lösung der Mischpolymerisat-Grundlage zusetzt und nuasl der Umsetzung das erhaltene Mischpolymerisat isoliert.
  • Gegenstand der Erfindung ist ein verbessertes Verfahren sur Modifixierung des Carbonsäuregruppen enthaltenden Mischpolymerisates, das sich dadurch kennzeichnet, das man die Polymerisatteilohen in einer Fltlssigkeit aufschlämmt, in welcher die mit den Carbonsäuregruppen reagierende Diamin-Komponente enthalten ist. Die Diaminkonzentration in der Fltlssigkeit beträgt vorzugsweise das 2. bis 4fache derjenigen Menge, die stöchiometrisch zur Neutralisation einer vorher festgelegten Menge an Carbonsäuregurppen des MIschpolymerisates, die Uber 10 ß liegt, notwendig ist Å12 α-Olefin in den Mischpolymerisaten kann man wenigstens ein α-Olefin der Formel RCH-CH2 verwenden, worin R Wasserstoff oder einenKohlenwasserstoffrest, bezonders einen Alkylrest, mit 1 bis 8 kohlenstoffatomen bedeutet. Vorzugsweise verwendet man Xthylen, Propylen, Buten-(1), Penten-(1), Hexen-(1), Hepten-(1), $Wethylubten-(1) und 4-Methylbuten-(1).
  • Die Temperatur der Aufschlämmung liegt vorzugsweise zwischen 50 unf 100°C. Die höheren Temperaturen innerhalb dieses Bereiches begünstigen eine schnellere Neutralisation, aber auch eine stärkere Fl üssigkeitsabsorption durch das Mischpolymerisat.
  • Die zum Aufschlämmen verwendete Flussigkeit kann jedes beliebig Lösungsmittel fur das Kationen liefernde Material sein; geeignete Lösungsmittel sind Wasser, das bevorzugt wird. niedere alisphatische Alkohole, beispielsweies Methanol, Äthanol, Propanol und Butanol und Mischungen dieser niederen aliphatisohen Alkohole untereinander und/oder mit Wasser.
  • Die Reaktionszeit hängt von der Temperatur, der Kationen-Konzentration, der Pellegtrösse des Mischpolymerisates und dem gewnnschten Neutralisationsgrad ab; die Zeit beträgt im allgemeinen 30 Minuten bis 8 Stunden.
  • Die Pelletgrösse des Mischplolymerisates ist nicht kritisch, bevorzugt werden jedoch Pellets mit einer Korngrösse von etwa 0,15 mm bis 4,76 mm.
  • In der Aufschlämmung liegt das Mischpolymerisat in einer Menge vor, die 10 bis 40 Gew.%, bezogen auf die Aufschlämmung, ausmacht.
  • Da etwas Flüssigkeit von den Pellets adsorbiert wird, muss diese aus den Pellegs wieder entfarnt werden. Dies @@@@ @@@ @@@@@@@ @@@@ @@@@ einer @@@ektionse@truders er@@@@@hen. in welchem die Flüssigkeit verdampft wird.
  • Das @@@@ende Beisplel erlä@@@@@@ @dung, ohn @@@@ ein, B e i s p i e l 11,34 kg eines Äthylen-Methacrylsäure-Mischpolymerisates, das 90 Gew% Äthylen und 10 Gew.% Methacrylsaure enthält und einen Schmelzindex von 5,8 g/10 Min., eine zerreissfestigkeit von 239,1 kg/cm2 und eine Dehnung von 550% aufweist, achlämmt man in 111,13 kg Methanol auf, das 1,36 kg Hexamethylendiamin enthält. Die Mischpolymerisat-Pellets haben eine solche Grösse, das sie durch ein Sieb mit einer Maschenweite von 0,84 mm gehen. Eine Analyse der flüssigen Phase zeigt, dass nach 2 Stunden 0,65 kg hexamethylendiamin mit den Säuregurppen reagiert haben. Das Mischpolymerisat ist transparenter und zäher als vor der Neutralisation. Der Schmelzindex ist im wesentlichen unverändert

Claims (5)

  1. P a t e n t a n s p r ü c h e 1. Verefahren zur herstellung. von modifizierten Mischpolymerisaten eines a-Olefins und einer äthylenisch α-ß-ungesättigten MOnocarbonsäure nach Patent . ... ... (Patentanmeldung P 15 20 518. 2 - ( P 31 004)), dadurch gekennzeichnet. dass man die Polymperisatteilchen in einer Flüssigkeit aufschlämmt, werche die mit den Carbonsäuregruppen reagierende Diamin-Komponente enthält.
  2. 2. Verfahren nach Anspruoh la: daduroh gekennzeichnet, dass man als Flussigkeit Wasser einsetzt.
  3. 3. Verfahren nach Anspruch 1 und/oder 2, daduroh gekennzeichnet, dass man die Vernetzung bei einer Temperatur zwischen 50 und 100°C durchführt.
  4. 4. Verfahren nach einem oder mehreren der Anspruche 1 bis 3. dadurch gekennzeichnet, dass man das zu vernetzende Polymerisat in Form von Pellets einsetzt, deren Krngrösse zwischen etwa 0,15 mm und 4,76 mm liegt.
  5. 5. Verfahren nach einem oder mehreren der Ansprüche 1 bis X, dadurch gekennzeichnet, dass die Flüssigkeit, in tieloher die Mischpolymeisatteilchen aufgeschlämmt werden, die mit den Carbonsäuregruppen reagierende Diaminkomponente in einer Menge enthält, die 2- bis 4-mal so gross ist wie diejenige Menge, die stöchiometrisch zur Neutralisation einer vorher festgelegten Menge an Carbonsäuregruppen des Mischpolymerisates, die Uber 10 % liegt, erforderlich ist.
DE1595112A 1961-08-31 1965-03-01 Verfahren zur Herstellung von modifizierten Copolymerisaten aus ungesättigten Kohlenwasserstoffen und ungesättigten Carbonsäuren Expired DE1595112C3 (de)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US13514761A 1961-08-31 1961-08-31
US16883962A 1962-01-25 1962-01-25
US27147763 US3264272A (en) 1961-08-31 1963-04-08 Ionic hydrocarbon polymers
US34829364 US3404134A (en) 1961-08-31 1964-02-28 Process of crosslinking polymers

Publications (3)

Publication Number Publication Date
DE1595112A1 true DE1595112A1 (de) 1970-04-09
DE1595112B2 DE1595112B2 (de) 1973-07-05
DE1595112C3 DE1595112C3 (de) 1974-03-14

Family

ID=27495141

Family Applications (6)

Application Number Title Priority Date Filing Date
DE1962P0030096 Pending DE1520506B2 (de) 1961-08-31 1962-08-27 Verfahren zum modifizieren von carboxylgruppen enthaltenden aethylenpolymeren
DE1963P0031004 Pending DE1520518B2 (de) 1961-08-31 1963-01-24 Verfahren zur herstellung von modifizierten copolymerisaten aus ungesaettigten kohlenwasserstoffen und ungesaettigten carbonsaeuren
DE1520601A Granted DE1520601B2 (de) 1961-08-31 1964-04-08 Verfahren zum Modifizieren von Carboxylgruppen enthaltenden Äthylenpolymeren
DE1745939A Expired DE1745939C3 (de) 1961-08-31 1965-03-01 Verfahren zum Modifizieren von Carboxylgruppen enthaltenden Äthylenpolymeren
DE1965P0036183 Granted DE1745938B2 (de) 1961-08-31 1965-03-01 Verfahren zum modifizieren von carboxylgruppen enthaltenden aethylenpolymeren
DE1595112A Expired DE1595112C3 (de) 1961-08-31 1965-03-01 Verfahren zur Herstellung von modifizierten Copolymerisaten aus ungesättigten Kohlenwasserstoffen und ungesättigten Carbonsäuren

Family Applications Before (5)

Application Number Title Priority Date Filing Date
DE1962P0030096 Pending DE1520506B2 (de) 1961-08-31 1962-08-27 Verfahren zum modifizieren von carboxylgruppen enthaltenden aethylenpolymeren
DE1963P0031004 Pending DE1520518B2 (de) 1961-08-31 1963-01-24 Verfahren zur herstellung von modifizierten copolymerisaten aus ungesaettigten kohlenwasserstoffen und ungesaettigten carbonsaeuren
DE1520601A Granted DE1520601B2 (de) 1961-08-31 1964-04-08 Verfahren zum Modifizieren von Carboxylgruppen enthaltenden Äthylenpolymeren
DE1745939A Expired DE1745939C3 (de) 1961-08-31 1965-03-01 Verfahren zum Modifizieren von Carboxylgruppen enthaltenden Äthylenpolymeren
DE1965P0036183 Granted DE1745938B2 (de) 1961-08-31 1965-03-01 Verfahren zum modifizieren von carboxylgruppen enthaltenden aethylenpolymeren

Country Status (9)

Country Link
US (2) US3264272A (de)
BE (2) BE627537A (de)
CH (2) CH445861A (de)
DE (6) DE1520506B2 (de)
DK (1) DK125713B (de)
FR (1) FR1430478A (de)
GB (4) GB1011981A (de)
NL (4) NL282755A (de)
SE (2) SE311229B (de)

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DK125713B (da) 1973-03-26
SE303882B (de) 1968-09-09
DE1520518A1 (de) 1969-07-03
DE1745938B2 (de) 1973-07-19
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US3264272A (en) 1966-08-02
NL129542C (de) 1900-01-01
DE1745939A1 (de) 1971-01-14
DE1745938C3 (de) 1974-02-21
NL282755A (de) 1900-01-01
DE1745939B2 (de) 1973-07-19
GB1029035A (en) 1966-05-11
DE1520506B2 (de) 1971-06-09
DE1745938A1 (de) 1971-01-14
DE1595112C3 (de) 1974-03-14
CH435741A (de) 1967-05-15
DE1745939C3 (de) 1974-02-21
GB1011981A (en) 1965-12-01
US3404134A (en) 1968-10-01
GB1063436A (en) 1967-03-30
SE311229B (de) 1969-06-02
DE1520601A1 (de) 1970-05-14
FR1430478A (fr) 1966-03-04
BE621846A (de) 1900-01-01
DE1520506A1 (de) 1970-02-19
DE1520601B2 (de) 1973-01-04
DE1595112B2 (de) 1973-07-05
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