DE2724363C3 - Aqueous isocyanate emulsions for gluing chipboard - Google Patents

Aqueous isocyanate emulsions for gluing chipboard

Info

Publication number
DE2724363C3
DE2724363C3 DE2724363A DE2724363A DE2724363C3 DE 2724363 C3 DE2724363 C3 DE 2724363C3 DE 2724363 A DE2724363 A DE 2724363A DE 2724363 A DE2724363 A DE 2724363A DE 2724363 C3 DE2724363 C3 DE 2724363C3
Authority
DE
Germany
Prior art keywords
chipboard
gluing
polyglycol
emulsion
emulsions
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
DE2724363A
Other languages
German (de)
Other versions
DE2724363B2 (en
DE2724363A1 (en
Inventor
Wolfgang Dipl.-Chem. Dr. 6904 Ziegelhausen Reuther
Adolph Dipl.- Chem. Dr. 6702 Bad Duerkheim Segnitz
Juergen Ing.(Grad.) 6940 Weinheim Winter
Otto Ing.(Grad.) 6710 Frankenthal Wittmann
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.)
BASF SE
Original Assignee
BASF SE
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 BASF SE filed Critical BASF SE
Priority to DE2724363A priority Critical patent/DE2724363C3/en
Priority to IT31357/77A priority patent/IT1090372B/en
Priority to NLAANVRAGE7800040,A priority patent/NL186170C/en
Priority to SE7800804A priority patent/SE440363B/en
Priority to CH73978A priority patent/CH633303A5/en
Priority to AT0058278A priority patent/AT370749B/en
Priority to DK38278A priority patent/DK148359C/en
Priority to FR7802356A priority patent/FR2378810A1/en
Publication of DE2724363A1 publication Critical patent/DE2724363A1/en
Publication of DE2724363B2 publication Critical patent/DE2724363B2/en
Application granted granted Critical
Publication of DE2724363C3 publication Critical patent/DE2724363C3/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C263/00Preparation of derivatives of isocyanic acid
    • C07C263/18Separation; Purification; Stabilisation; Use of additives
    • 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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/10Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • 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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/4833Polyethers containing oxyethylene units
    • 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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/62Polymers of compounds having carbon-to-carbon double bonds
    • C08G18/6212Polymers of alkenylalcohols; Acetals thereof; Oxyalkylation products thereof
    • 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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/703Isocyanates or isothiocyanates transformed in a latent form by physical means
    • C08G18/705Dispersions of isocyanates or isothiocyanates in a liquid medium
    • C08G18/706Dispersions of isocyanates or isothiocyanates in a liquid medium the liquid medium being water

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Dispersion Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Description

Die Erfindung nach der Patentschrift 27 03 271 betrifft ein Verfahren zur Herstellung wäßriger Polyisocyanatemulsionen, wobei man die Polyisocyanate in Gegenwart eines Emulgator* auf der Grundlage eines Polyglykols mit einem Molekulargewicht von etwa 4000 his 20 000, wobei die OH-Gruppen im Emulgator 40% oder weniger der NCO-Gruppen ausmachen, in Wasser dispergiert bzw. emulgiert.The invention according to patent specification 27 03 271 relates to a process for the production of aqueous Polyisocyanate emulsions, the polyisocyanates in the presence of an emulsifier * based on a polyglycol with a molecular weight from about 4000 to 20,000, with the OH groups in the emulsifier being 40% or less of the NCO groups make up, dispersed or emulsified in water.

Die Erfindung betrifft eine weitere Ausgestaltung des Verfahrens nach dem Hauptpatent, indem man zusätzlich 1 bis 30 Gewichtsprozent, bezogen auf das Polyglykoi, eines Polypeptids verwendet.The invention relates to a further embodiment of the method according to the main patent by additionally 1 to 30 percent by weight, based on the polyglycol, of a polypeptide is used.

Gegenstand des Patents ist somit ein Verfahren zur Herstellung wäßriger Polyisocyanatemulsionen durch Emulgieren bzw. Dispergieren der Polyisocyanate in Wasser in Gegenwart von Emulgatoren auf Grundlage eines Polyglykols mit einem Molekulargewicht von etwa 4000 bis 20 000, wobei die OH Gruppen im Emulgator 40% oder weniger der NCO-Gruppen ausmachen nach Patent 27 03 271, dadurch gekennzeichnet, daß man 1 bis 30% eines Polypeptides bezogen auf das Polyglykol mitverwendet. The subject of the patent is thus a process for the preparation of aqueous polyisocyanate emulsions by emulsifying or dispersing the polyisocyanates in water in the presence of emulsifiers based on a polyglycol with a molecular weight of about 4000 to 20,000, the OH groups in the emulsifier make up 40% or less of the NCO groups according to patent 27 03 271, characterized in that 1 to 30% of a polypeptide based on the polyglycol is also used.

Es entstehen wäßrige Emulsionen von Polyisocyanaten, die gegenüber den nach dem Hauptpatent erhältlichen eine gesteigerte Gebrauchsdauer besitzen und überdies preiswerter sind, da /u ihrer Herstellung weniger Emulgator benötigt wird. Im allgemeinen ist •sine Menge von etwa 03 bis 5% Emulgator, bezogen auf das gesamte Emulsionsgewicht ausreichend, um eine Emulsion herzustellen, deren litrierbarer Gehalt an Isocyanatgruppen in 10 Stunden um nicht mehr als etwa 3% abfallt. Die nachstehende Tabelle, die mit der Emulsion des Herstellbeispiels aufgestellt wurde, /eigi dies.Aqueous emulsions of polyisocyanates are formed which have a longer useful life than those obtainable according to the main patent and, moreover, are cheaper because less emulsifier is required for their production. In general, • sine amount of about 03-5% of emulsifier, based on the total emulsion weight sufficient to produce an emulsion whose litrierbarer content does not fall away more than about 3% of isocyanate groups in 10 hours to. The table below, which was drawn up with the emulsion of the preparation example, / Eigi dies.

Polypeptide im Sinne der Erfindung sind beispielsweise Gelatine. Knochenleime und ähnliche aus Eiweißkörpern gewinnbare Produkte, Diese sind handelsüblich und bedürfen keiner näheren Erläuterung. Sie werden bevorzugt dem Emulgierwasser in entsprechender Konzentration zugesetzt und lassen eine hohe Emulgiergeschwindigkeit zu. Im allgemeinen beträgt der Gehalt an Polyglykol in der Emulsion 1 bis 10%, während 0,1 bis 1 % Polypeptid verwendet werden,Polypeptides in the context of the invention are, for example, gelatin. Bone glue and the like made from protein bodies winnable products, these are commercially available and do not require any further explanation. you will be preferably added to the emulsification water in the appropriate concentration and allow a high emulsification rate to. In general, the content of polyglycol in the emulsion is 1 to 10%, while 0.1 to 1% polypeptide is used,

Angaben zu sonstigen Einzelheiten zur Herstellung und Verwendung der Polyisocyanatemulsionen sind inInformation on other details on the production and use of the polyisocyanate emulsions can be found in

ίο der Beschreibung des Hauptpatents enthalten, auf die hier verwiesen wird.ίο included in the description of the main patent to which referenced here.

Beispielexample

Eine typische Emulsion wird aus 38 Teilen technischem Diphenylmethan-4,4'-diisocyanat (MDt) und 62 Teilen 3,5%iger wäßriger Emulgatorlösung in folgenderA typical emulsion is made up of 38 parts technical Diphenylmethane-4,4'-diisocyanate (MDt) and 62 parts of 3.5% strength aqueous emulsifier solution in the following

Weise erhalten:
Es wird eine 3,5%ige Lösung aus 0,5 Teilen i~"-Älatine
Way to get:
It becomes a 3.5% solution of 0.5 parts of i ~ "-älatine

und 3 Teilen eines Polyglykols in warmem Wasser hergestellt. In 62 Teile der abgekühlten Lösung werden 38 Teile Diphenylmethan-4,4'-diisocyanat eingerührt.and 3 parts of a polyglycol in warm water. Be in 62 parts of the cooled solution 38 parts of diphenylmethane-4,4'-diisocyanate were stirred in.

Das Emulgieren miiteis eines hochtourigen Rührwerks erfordert ca. 10 bis 15 Sekunden.Emulsification with a high speed stirrer takes about 10 to 15 seconds.

Zur Bestimmung der Stabilität der Emulsion wird der 2-, Isocyanatgehalt zum Zeitpunkt der Herstellung gleich 100% gesetzt und die Abnahme laufend gemessen. So ergibt sich bei der beschriebenen 38%igen Emulsion inerhalb von 7 Stunden nur eine Abnahme von 2,6%To determine the stability of the emulsion, the 2, isocyanate content is the same at the time of manufacture 100% set and the decrease measured continuously. This results in the 38% emulsion described only a decrease of 2.6% within 7 hours

Klebstoffgehalt.
mi Die folgende Tabelle gibt eine Übersicht über die gemittelten Isocyanatgehalte für eine Emulsion aus 38 Teilen DiphenyImethan-4,4'-diisocyanat mit 62 Teilen 3,5%iger wäßriger Emulgatorlösung.
Adhesive content.
The following table gives an overview of the averaged isocyanate contents for an emulsion of 38 parts of diphenymethane-4,4'-diisocyanate with 62 parts of 3.5% strength aqueous emulsifier solution.

>'> Tabelle> '> Table

Stundenhours

Isocyunat (%)Isocyanate (%)

0
0,5
0
0.5

I
2
3
4
5
6
7
I.
2
3
4th
5
6th
7th

100,0
99,8
99,5
99,0
98,6
98,4
97,8
97,6
97,4
100.0
99.8
99.5
99.0
98.6
98.4
97.8
97.6
97.4

AnwendungsbeispielApplication example

Mit Her beschriebenen Emulsion, die mittels 5%iger Emulgatorlösung erhalten worden war, wurden in üblicher Weise Spanplatten hergestellt und ihre technologische Anwendung geprüft.With her described emulsion, which means 5% Emulsifier solution had been obtained, particle board was produced in the usual way and their technological application checked.

Isdcyanal her. 100% auf absolut trockene (aim) SpiincIsdcyanal. 100% absolutely dry (aim) Spiinc

Plattenprüfung nach DIN 52 360-65
Biegefestigkeit (N/mm')
Ouerzugfestigkeil V 20 (kp/cm2)
Querzugfestigkeit V KK) (kp/cnv)
Quellung n. 2 h (%)
Qucllung n. 24 h (%)
Plate test according to DIN 52 360-65
Flexural Strength (N / mm ')
Tensile strength wedge V 20 (kp / cm 2 )
Transverse tensile strength V KK) (kp / cnv)
Swelling after 2 h (%)
Swelling after 24 h (%)

27»27 »

.1%.1%

4%4%

21.221.2 23,423.4 26,226.2 .M.M 5,95.9 7,97.9 0.20.2 1,41.4 2,42.4 2.42.4 2.42.4 2,22.2 12.012.0 9.09.0 8.48.4

Claims (1)

Patentanspruch:Claim: Verfahren zur Herstellung wäßriger Polyisocyanatemulsionen durch Emulgieren bzw. Dispergieren der Polyisocyanate in Wasser in Gegenwart von Emulgatoren auf Grundlage eines Polyglykols mit einem Molekulargewicht von etwa 4000 bis 20 000, wobei die OH-Gruppen im Emulgator 40% oder weniger der NCO-Gruppen ausmachen nach Patent 2703271, dadurch gekennzeichnet, daß man 1 bis 30% eines Polypeptides bezogen auf das Polyglykol mitverwendet. Process for the preparation of aqueous polyisocyanate emulsions by emulsifying or dispersing the polyisocyanates in water in the presence of Emulsifiers based on a polyglycol with a molecular weight of about 4,000 to 20,000, where the OH groups in the emulsifier make up 40% or less of the NCO groups Patent 2703271, characterized in that 1 to 30% of one Polypeptides based on the polyglycol are also used.
DE2724363A 1977-01-27 1977-05-28 Aqueous isocyanate emulsions for gluing chipboard Expired DE2724363C3 (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
DE2724363A DE2724363C3 (en) 1977-05-28 1977-05-28 Aqueous isocyanate emulsions for gluing chipboard
IT31357/77A IT1090372B (en) 1977-01-27 1977-12-28 ISOCYANATE WATER EMULSIONS FOR GLUING OF CHIPBOARD SHEETS
NLAANVRAGE7800040,A NL186170C (en) 1977-01-27 1978-01-02 PROCESS FOR PREPARING AQUEOUS POLYISOCYANATE MULSIONS AND FORMED PRODUCT, PREPARED USE THEREOF
SE7800804A SE440363B (en) 1977-01-27 1978-01-23 PROCEDURE FOR THE PREPARATION OF A CHEESE PATCH ADJUSTABLE POLYISOCYANATE EMULSION
CH73978A CH633303A5 (en) 1977-01-27 1978-01-24 Process for the preparation of aqueous polyisocyanate emulsions
AT0058278A AT370749B (en) 1977-01-27 1978-01-26 METHOD FOR PRODUCING AQUEOUS POLYISOCYANATE EMULSIONS
DK38278A DK148359C (en) 1977-01-27 1978-01-26 PROCEDURE FOR MANUFACTURING Aqueous POLYISOCYANATE EMULSIONS FOR LIMITING CHIPBOARDS
FR7802356A FR2378810A1 (en) 1977-01-27 1978-01-27 AQUEOUS ISOCYANATE EMULSIONS FOR BONDING AGGLOMERATE PANELS

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE2724363A DE2724363C3 (en) 1977-05-28 1977-05-28 Aqueous isocyanate emulsions for gluing chipboard

Publications (3)

Publication Number Publication Date
DE2724363A1 DE2724363A1 (en) 1978-11-30
DE2724363B2 DE2724363B2 (en) 1979-11-15
DE2724363C3 true DE2724363C3 (en) 1980-07-31

Family

ID=6010218

Family Applications (1)

Application Number Title Priority Date Filing Date
DE2724363A Expired DE2724363C3 (en) 1977-01-27 1977-05-28 Aqueous isocyanate emulsions for gluing chipboard

Country Status (1)

Country Link
DE (1) DE2724363C3 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2921681A1 (en) * 1979-05-29 1980-12-11 Bayer Ag NEW EMULSIFIERS, AQUEOUS ISOCYANATE EMULSIONS CONTAINING THESE EMULSIFIERS AND THE USE THEREOF AS BINDERS IN A METHOD FOR PRODUCING MOLDED BODIES
DE2921726A1 (en) * 1979-05-29 1980-12-11 Bayer Ag AQUEOUS ISOCYANATE EMULSIONS AND THE USE THEREOF AS BINDERS IN A METHOD FOR PRODUCING MOLDED BODIES
DE3700245A1 (en) * 1987-01-07 1988-07-21 Basf Ag METHOD FOR PRODUCING LIGHT, FLAT-SHAPED MOLDED PARTS USING AQUEOUS DISPERSIONS OR EMULSIONS FROM ORGANIC COMPOUNDS HAVING NCO GROUPS, AND MOLDED PARTS MADE BY THE METHOD

Also Published As

Publication number Publication date
DE2724363B2 (en) 1979-11-15
DE2724363A1 (en) 1978-11-30

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Legal Events

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OAP Request for examination filed
OD Request for examination
C3 Grant after two publication steps (3rd publication)
8340 Patent of addition ceased/non-payment of fee of main patent