CA2253119A1 - Hydrophilizing agent precursor, a process for its preparation and its use as a dispersing agent for aqueous polyurethane dispersion - Google Patents

Hydrophilizing agent precursor, a process for its preparation and its use as a dispersing agent for aqueous polyurethane dispersion Download PDF

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CA2253119A1
CA2253119A1 CA002253119A CA2253119A CA2253119A1 CA 2253119 A1 CA2253119 A1 CA 2253119A1 CA 002253119 A CA002253119 A CA 002253119A CA 2253119 A CA2253119 A CA 2253119A CA 2253119 A1 CA2253119 A1 CA 2253119A1
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polyurethane dispersion
hydrophilizing agent
agent
precursor
hydrophilizing
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Eberhard Konig
Detlef-Ingo Schutze
Jurgen Meixner
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Bayer AG
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Bayer AG
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/2805—Compounds having only one group containing active hydrogen
    • C08G18/2815—Monohydroxy compounds
    • C08G18/283—Compounds containing ether groups, e.g. oxyalkylated monohydroxy compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C229/06—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton
    • C07C229/10—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings
    • C07C229/14—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings to carbon atoms of carbon skeletons containing rings
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/0804—Manufacture of polymers containing ionic or ionogenic groups
    • C08G18/0819—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups
    • C08G18/0823—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups containing carboxylate salt groups or groups forming them
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/44—Polycarbonates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/48—Polyethers
    • C08G18/4854—Polyethers containing oxyalkylene groups having four carbon atoms in the alkylene group
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/80—Masked polyisocyanates
    • C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
    • C08G18/807—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with nitrogen containing compounds
    • C08G18/8077—Oximes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04—Polyurethanes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14—The ring being saturated

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  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
  • Paints Or Removers (AREA)
  • Polyurethanes Or Polyureas (AREA)
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Abstract

A new hydrophilizing agent precursor made by Michael addition of 1-amino-3,3,5-trimethyl-5-aminomethyl-cyclohexane with an .alpha.,.beta.-unsaturated carboxylic acid; its preparation and use, particularly as a dispersing agent in aqueous polyurethane dispersions.

Description

CA 022~3119 1998-11-09 Le A 32 640-US Eck/ng~/N l / v /~.u~

HYDROP~IT,17,1NG AGENT PRECURSOR, A PROCESS FOR ITS PREP-ARATION AND ITS USE AS A DISPERSING AGENT FOR AQUEOUS
POLYURETHANE DISPERSION

FIELD OF THE INVENTION
The present invention relates to a new hydrophilizing agent and its preparation and use, in particular as a dispersing agent in aqueous polyurethane dispersions.

BACKGROUND OF THE INVENTION
lû It is known that NCO prepolymers are hydrophilized by reaction with suitable molecules with ionic groups, e.g., carboxylate anions. It is also known that poly-urethanes hydrophilized in this way can be converted into polyurethane plastics which can then be dispersed in water for the production of coatings for substrates such as textiles, sheet metals, stone or wood. A review article by Rosthauser and Nachtkamp in "Advances in Urethane Science and Technology", Volume lû, page 121 - 162 (1987) summarizes the knowledge in this field.

ACS Registry Number 8454û-26-1 discloses ~-AIanine, N-[(5-amino-1,3,3-trimethylcyclohexyl)methyl]-,monopotassium salt. British Patent 1,339,357, (British 2û version of DE-A 2,û34,479), discloses dispersing agent building blocks made with the alkali metal salt of the addition product of an a-olefinic carboxylic acid, i.e., acrylic acid, and an aliphatic diprimary diamine. Alkali metal salts used to make the alkali metal salt of the addition product of an a-olefinic carboxylic acid and adiamine are prepared from the hydroxides, carbonates or bicarbonates of sodium, potassium or lithium. The alkali metal salts are critical, and there is no suggestion that the polyurethane lattices can be made without the alkali metal salt of the addition product of an a-olefinic carboxylic acid and a diamine. There is no suggestion that cyclic diamines, e.g., isophorone diisocyanate, can be used. The agents can be used to make polyurethane lattices, which when dried, are intended to have little tendency 3û to swell in water and suitable resistance to water. To make the polyurethane lattices, a prepolymer containing isocyanate group reacts with the alkali metal salt of the LeA32640-US CA 022~3119 1998-11-09 addition product of an a-olefinic carboxylic acid and an aliphatic diamine.

These agents are disadvantageous because they are permanently hydrophilized (dueto the presence of the non-volatile base content, e.g., sodium), and do not have the lower hydrophilicity that is desired in some applications. Correspondingly, the coatings formed by the dispersing agents after being applied and stoving of a polyurethane dispersion such that the textile coatings or the lacquers produced with them still have an increased sensitivity to water. It would be desired to develop a hydrophilizing agent sufficiently versatile so that it can have either temporary hydro-philicity or permanent hydrophilicity. Another disadvantage of this group of dispersing agents is the intense yellow-brown intrinsic color, which manifests itself noticeably in a troublesome manner in pale-colored coatings.

The object of the invention is to overcome the disadvantages above, and therefore provide a dispersing agent which on the one hand is colorless and on the other hand can be temporarily hydrophilized or permanently hydrophilized. It is a further object of the invention to develop a simple process for making the dispersing agent. This object has been achieved with the discovery of the compound according to the invention.
SUMMARY OF THE INVENTION
The invention relates to a hydrophilizing agent precursor prepared by the Michael addition of 1-amino-3,3,5-trimethyl-5-aminomethyl-cyclohexane with an oc,~-unsaturated carboxylic acid. The term "Michael Addition" is known and refers to the overall addition to a"B-unsaturated carbonyl compounds in which an a,~-unsaturated carbonyl compound undergoes a nucleophilic attack at the end of the double bond further from the carbonyl group. The hydrophilizing agent precursor can be perma-nently or temporarily neutralized to form a hydrophilizing agent, depending on the desired application. The invention also relates to the use of the hydrophilizing agent as a chain lengthener of NCO prepolymers for use in the preparation of an aqueous polyurethane dispersion. The invention also relates to a hydrophilized polyurethane coating on a substrate, e.g., leather and textiles.

LeA32640-US CA 022~3119 1998-11-09 DETAILED DESCRIPTION OF THE INVENTION
The invention relates to a hydrophilizing agent precursor prepared by Michael addition of 1-amino-3,3,5-trimethyl-5-aminomethyl-cyclohexane with an a,~-unsaturated carboxylic acid. IPDA is a known compound which can be obtained 5 from commercial sources. The a,~-unsaturated carboxylic acids include but are not limited to acrylic acid, methacrylic acid or crotonic acid and can also be obtained commercially. Generally, the a"~-unsaturated carboxylic acid is used in an amount ranging from 1 to 2 mol. Specific amounts are given in the examples below or canbe readily obtained with routine experimentation. The fact that an a"B-unsaturated 10 acid is reacted directly with IPDA and that this reaction product is a storage stable, almost colorless compound is essential to the invention. This storage-stable compound can be incorporated into NCO prepolymer chains and then neutralized.

Preferably, the invention relates to the Michael addition product of IPDA and acrylic 15 acid, in which a compound mixture of unreacted IPDA, mono-adduct and di-adduct forms. The mono-adduct predominantly formed has the formula ~ CH--NH CH2--CH2 COOM
in which M represents H, an alkali/alkaline earth metal, such as Na, K, "2Ca or "2Mg, or an amine moiety. Suitable amine moieties include NH4+ and N(R)3, where R
is methyl, ethyl and/or hydroxyether.

25 The hydrophilizing agent precursor of the invention is neutralized permanently or temporarily, depending on the needs of a specific application. Suitable neutralizing agents for temporary hydrophilization include but are not limited to (i) volatile tertiary amines, e.g., dimethyl ethanol amine or triethylamine, and (ii) diprimary CA 022~3119 1998-11-09 Le A 32 640-US

amines which can be incorporated by isophoronediamine or 4,4' diamino-dicyclohexylmethane, and the like. Suitable neutralizing agents for permanently hydrophilization include metal bases, e.g., alkali/alkaline earth metal hydroxide.
Generally, the neutralizing agent is used in an amount up to the equivalent of the 5 COOH groups. Specific amounts of the neutralizing agent are given in the examples below or can be readily obtained with routine experimentation.

The hydrophilizing agent precursor according to the invention can be used in anyway to meet the objects of the invention. The hydrophili7.ing agent precursors 10 according to the invention, for instance, can be prepared by first introducing 1 mol of IPDA into a reaction vessel, preferably in water or isopropanol. ~,~-unsaturated car-boxylic acid, e.g., acrylic acid, can then be added dropwise into the reaction vessel at room temperature with stirring. The reaction manifests itself by a slight exothermicity. After the addition of the acid, the mixture is subsequently stirred at 15 40~C for 1 hour, and a clear colorless solution results. The clear and colorless solution of the hydrophilizing agent can then be suitably employed. For example, the solution can be added in a suitable amount to an acetonic NCO prepolymer solution at approx. 40~C, so that the hydrophilizing agent becomes incorporated into the polyurethane chains. Neutralization is then carried out with the calculated amount of 20 base. It can then be decided whether a permanent hydrophilization, that is to say a neutralization with non-volatile metal hydroxides, or only a temporary hydrophilization, e.g., without an alkali metal. That is to say a neutralization with amines, is desired. An acetonic polyurethane solution can be dispersed in water in accordance with known techniques and further processed into an aqueous 25 polyurethane dispersion for coatings by removal of the acetone by distillation. The preparation method generally does not utilize acyclic diamines. Specific amountscan be obtained by routine experimentation. Coatings can be made by applying thedispersion over a suitable substrate and drying the dispersion at a suitable temperature, e.g., 80~C.
The resulting film (coating) has properties which are suitable for substrates such as LeA32640-US CA 022~3119 1998-11-09 textile materials, paper, plastics, metals, and glass. Film properties can be characterized by determining the film's modulus, tensile dry strength, elongation at break dry, tensile wet strength, elongation at break wet, and the like. Example S
below shows film properties of a coating prepared in accordance to the invention.
5 Properties of other coatings can be determined by routine experimentation.

As already mentioned in part, the hydrophilizing agents according to the invention have the following advantageous properties:
- easy preparation 10 - no yellow coloration, and instead colorlessness - possibility of choice of salt formation with non-volatile bases (metal hydroxides) or with volatile bases (amines) - good compatibility with NCO prepolymers - extension of the range of carboxylate-containing dispersing agents available.
The last two points are explained as follows. Carboxylate-containing hydrophiIizing agents have a weaker permanent hydrophilicity than sulfonate-containing hydrophilizing agents, and for this reason the former are also preferred for aqueous lacquer applications or textile coatings with a high level of properties. However, 20 only few such hydrophilization building blocks exist on the market, such as carboxylate-containing compounds of dimethylolpropionic acid.

The hydrophilizing agents according to the invention supplement the range available in this respect and extend the possibilities of combinations of chemicals, because the 25 new hydrophilizing components are based on the IPDA hard segment, which is known to have a good compatibility. They are therefore particularly suitable forcoating surfaces of the most diverse working substances and materials, e.g., textile materials, paper, plastics, metals, glass, etc., can be coated with them.

30 The invention is further described in the following illustrative examples. All parts are by weight unless otherwise indicated.

LeA32640-US CA 022~3119 1998-11-09 EXAMPLES
Example 1 Batch:
85.0 g (1 eq NH2)* isophoronediamine 36.0 g (0.5 mol) acrylic acid 282.0 g water 403.0 g (1 eq NH/NH2) dispersing agent solution solids: calc. 30%
1 acid equivalent: 806 g * based on the C=C double bond Procedure:

IPDA and water were initially introduced into the reaction vessel at room 5 temperature. Acrylic acid was added dropwise to this mixture, while stirring, the mixture warming slightly. When the addition of the acrylic acid has ended, the mixture was subsequently stirred at 45~C for 1 hour. A clear, colorless dispersing agent solution (30%) with an NH/NH2 equivalent weight of 403 g and an acid equivalent of 806 g was obtained.
This dispersing agent solution can also easily be prepared in concentrated form, for example 50 or 60%. However, there was then the risk of crystallizing out at roomtemperature. Nevertheless, if these high-solids variants were stored at 60 to 70~C, they also remain liquid.

LeA32640-US CA 022~3119 1998-11-09 Example 2 (use example) Batch:
235.0 g (0 236 eq) of a polycarbonate based on hexane-1,6-diol of OH number 56 80.0 g (0.080 eq) of a polytetramethylene glycol of OH
number 56 10.0 g (0.020 eq) of a monofunctional ethylene oxide polyether of molecular weight 500 4.3 g (0.064 eq) dimethylpropionic acid 33.6 g (0.400 eq) 1,6-diisocyanatohexane (HDI) 35.6 g (0.320 eq) 1 -isocyanato-3,3,5-trimethyl-5-isocyanato-methyl-cyclohexane (IPDI) 28.2 g (0.070 eq) dispersing agent according to Example 1 7.65 g (0.090 eq) 1-amino-3,3,5-trimethyl-5-aminomethyl-cyclohexane (IPDA) 8.08 g (0.08 eq) triethylamine 612.0 g water 1,055.43 g dispersion (40%) viscosity (23~C) approx. 900 mPa s Procedure:

The above polyols were dewatered at 100~C under 40 mbar for 30 min. and cooled to approx. 90~C. The two diisocyanates were added all at once, while stirring, and the reaction was carried out at 90~C for approx. 2 hours. An NCO content of 3.2% wasmeasured, the calculated content being 3.36%. The mixture was diluted with 400 gacetone and a mixture of aqueous dispersing agent solution, IPDA and triethylamine was added to the acetonic NCO prepolymer solution, which has been heated to approx. 45~C. Thereafter, the mixture was subsequently stirred at 45~C for approx.

CA 022~3119 1998-11-09 Le A 32 640-US

another 1 hour and dispersed with water. After the acetone has been distilled off (45~C/100 mbar), a milky-blue dispersion with a solids content of approx. 40% and a viscosity (23~C) of approx. 900 mPa-s was obtained.

5 As a leather coating, the dispersion has suitable fastnesses to creasing, in particular cold creasing (over 10,000 at -10~C and -30~C).

Example 3 lO This example describes the preparation of the hydrophilizing agent in an organic solvent.

Batch:
170.0 g (2.0 eq) isophoronediamine 72.0 g (l.0 mol) acrylic acid 358.0 g isopropanol 600.0 g (2.0 eq NH/NH2) dispersing agent solution solids: calc. approx. 40%
l acid equivalent: calc. 600 g l 5 Procedure:

Isophoronediamine and isopropanol were initially introduced into the reaction vessel and heated up to 40~C. Acrylic acid was added dropwise to this mixture, while stirring, a slight exothermicity being observed. After the addition of the acrylic acid, 20 the mixture was subsequently stirred at 45~C for 2 hours. A ready-to-use colorless dispersing agent solution with an NH/NH2 equivalent of 300 g and an acid equivalent of 600 g was obtained .

LeA32640-US CA 022~3119 1998-11-09 Example 4 (according to the invention) In contrast to Example 1, there is a 10% neutralization of the carboxyl groups with KOH here.

Batch:
85.0 g (1 eqNH2) isophoronediamine 36.0 g (0.5 mol) acrylic acid 282.2g water 2.8 g (0.05 mol) potassium hydroxide 406.0 g (1.0 eq NH/NH2) dispersing agent solution solids: calc. approx. 30.1%
1 acid equivalent: 902 g Procedure:

10 The procedure was as described in Example 1, and when the reaction has ended, the stated amount of solid potassium hydroxide was also stirred in. A clear, colorless dispersing agent solution (approx. 30%) which already contains permanent salt groups to the extent of 10 equivalent % and also 90 equivalent % non-neutralizedcarboxyl groups was obtained. The equivalent weight, based on the NH or NH2 groups was 406 g.

Example 5 (use example) In this example, neutralization of the dispersing agent was carried out to the extent of 20 30 equivalent % with 4,4'-diamino-dicyclohexyl-methane, which was incorporated during curing (heat) of the coating. Consequently, a permanent hydrophilization of only 10 equivalent % on the part of the KOH exists in the cured coating.

LeA32640-US CA 022~3119 1998-11-09 Batch:
49.5 g (0.022 eq) of a monofunctional ethylene oxide/propylene oxide polyether of OH
number 25 80.0 g (0.080 eq) of a polypropylene glycol of OH number 110.0 g (0.110 eq) of a polycarbonate based on 1,6-dihydroxyhexane of OH number 56 110.0 g (0.110 eq) of a propylene oxide polyether started on trimethylolpropane of OH number 56 76.5 g (0.612 g) 4,4'-diisocyanato-diphenylmethane 12.18 g (0.14 eq) butanone oxime 60.90 g (0.15 eq) dispersing agent according to Example 4 14.70 g (0.14 eq) 4,4'-diamino-dicyclohexylmethane 533 57 water 1047.35 g dispersion solids: 45%
viscosity (23~C): approx. 500 mPa s Procedure:

5 The above polyols were dewatered at 100~C under 20 mbar and cooled to approx.
60~C. Thereafter, the total amount of polyurethane MDI was added all at once, while stirring, the mixture was heated slowly to 70~C and the reaction was carried out at this temperature for approx. 3 hours, until the NCO content has fallen to approx.
2.75%, an NCO content of 2.86% being calculated. The mixture was diluted with 500 g acetone and brought to approx. 40~C, and another control NCO measurement was carried out. An NCO content of approx. 1.2% was found, the calculated content being 1.3%. Thereafter, butanone oxime was added, the mixture was stirred at 40~C
for approx. 20 min and an NCO content of approx. 0.58% was determined, the LeA32640-US CA 022~3119 1998-11-09 calculated content being 0.67%. The dispersing agent solution according to Example 4 was then added and the mixture was subsequently stirred at 40~C for approx. 30min, until no further NCO content was detectable. The diamine was now stirred in, and after approx. 15 min. the mixture was dispersed with water. After the acetone 5 has been distilled off (45~C/100 mbar), a milky-blue dispersion with a solids content of 45% and a viscosity at 23~C of approx. 500 mPa s was obtained. In spite of the potentially reactive character, the dispersion was stable on storage.

Properties of the coating from the above dispersion 10 The dispersion was processed to a film or a gluing layer between PVC and polyamide according to a particular drying program (approx. I min. 80~C, approx. 1 min. 120~C and approx. 1 min. 140~C).

Film properties:
100% modulus 2.3 MPa Tensile strength dry 11.0 MPa Elongation at break dry 490%
Tensile strength wet 8.8 MPa Elongation at break wet 510%
Swelling vol. EE 502%
Swelling vol. H2O 33%
Film weight 70 g/m2 Adhesive strength on polyamide:
dry (N/2.5 cm) 34 wet (N/2.5 cm) 18 Although the invention has been described in detail in the foregoing for the purpose of illustration, it is to be understood that such detail is solely for that purpose and that variations can be made therein by those skilled in the art without departing from the spirit and scope of the invention.

Claims (12)

1. A method for making an aqueous polyurethane dispersion comprising the sequential steps of:

(a) reacting (i) 1-amino-3,3,5-trimethyl-5-amino-methyl-cyclohexane with (ii) an .alpha.,.beta.-unsaturated carboxylic acid to form a hydrophilizingagent precursor; and (b) adding the hydrophilizing agent precursor to an NCO prepolymer solution, (c) adding a neutralizing agent to the prepolymer solution in an amount up to the equivalent of the COOH groups to form the hydrophilizing agent, the neutralizing agent comprising a component selected from the group consisting of alkali/alkaline earth metal hydroxides and amines.

(d) dispersing the polyurethane solution in water to form the polyurethane dispersion.
2. The method of Claim 1, wherein the .alpha.,.beta.-unsaturated carboxylic acid is used in an amount ranging from about 1 to 2 moles.
3. The method of Claim 1, wherein the .alpha.,.beta.-unsaturated carboxylic acidcomprises a component selected from the group consisting of acrylic acid, methacrylic acid and crotonic acid.
4. The method of Claim 1, wherein the hydrophilizing agent comprises a component having the formula:

wherein M consists of an alkaline metal and an amine moiety.
5. The method of Claim 1, wherein the method does not utilize acyclic diamines.
6. The method of Claim 1, wherein the method does not utilize an alkali metal as a neutralizing agent.
7. The hydrophilizing agent used to make the polyurethane dispersion of Claim 6.
8. The polyurethane dispersion formed by the method of Claim 1.
9. A coating formed by applying the polyurethane dispersion of Claim 8 on a substrate to form a liquid coating and drying the liquid coating.
10. The coating of Claim 9, wherein the substrate comprises a component selected from the group consisting of textile materials, paper, plastics, metals, and glass.
11. A method for making an aqueous polyurethane dispersion by (a) combining a hydrophilizing agent with an NCO prepolymer solution, and (b) dispersing the polyurethane dispersion in water;

wherein the hydrophilizing agent is made by:

(i) reacting (i) 1-amino-3,3,5-trimethyl-5-amino-methyl-cyclohexane with (ii) an .alpha.,.beta.-unsaturated carboxylic acid to form a hydrophilizingagent precursor; and (ii) adding a neutralizing agent to the precursor solution in an amount up to the equivalent of the COOH groups to form the hydrophilizing agent, the neutralizing agent comprising a component selected from the group consisting of alkali/alkaline earth metal hydroxides and amines.
12. The dispersion of Claim 11.
CA002253119A 1997-11-13 1998-11-09 Hydrophilizing agent precursor, a process for its preparation and its use as a dispersing agent for aqueous polyurethane dispersion Abandoned CA2253119A1 (en)

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DE19750186A DE19750186A1 (en) 1997-11-13 1997-11-13 Hydrophilizing agent, a process for its preparation and its use as a dispersant for aqueous polyurethane dispersions
DE19750186.9 1997-11-13

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