WO2012089827A1 - Soft touch coating composition - Google Patents

Soft touch coating composition Download PDF

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Publication number
WO2012089827A1
WO2012089827A1 PCT/EP2011/074270 EP2011074270W WO2012089827A1 WO 2012089827 A1 WO2012089827 A1 WO 2012089827A1 EP 2011074270 W EP2011074270 W EP 2011074270W WO 2012089827 A1 WO2012089827 A1 WO 2012089827A1
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WO
WIPO (PCT)
Prior art keywords
diisocyanate
coating composition
soft touch
touch coating
composition according
Prior art date
Application number
PCT/EP2011/074270
Other languages
French (fr)
Inventor
Hu SHENGKUI
Original Assignee
BECKERS HIGH PERFORMANCE COATINGS (TIANJIN) Ltd.
BECKER INDUSTRIAL COATINGS (GUANGZHOU) Ltd.
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Application filed by BECKERS HIGH PERFORMANCE COATINGS (TIANJIN) Ltd., BECKER INDUSTRIAL COATINGS (GUANGZHOU) Ltd. filed Critical BECKERS HIGH PERFORMANCE COATINGS (TIANJIN) Ltd.
Publication of WO2012089827A1 publication Critical patent/WO2012089827A1/en

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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D175/00Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04Polyurethanes
    • C09D175/06Polyurethanes from polyesters
    • 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
    • C08G18/42Polycondensates having carboxylic or carbonic ester groups in the main chain
    • 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
    • C08G18/42Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/44Polycarbonates
    • 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
    • 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
    • C08G18/4854Polyethers containing oxyalkylene groups having four carbon atoms in the alkylene group
    • 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
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/80Masked polyisocyanates
    • C08G18/8003Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen
    • C08G18/8045Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with water
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D175/00Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04Polyurethanes
    • C09D175/08Polyurethanes from polyethers

Definitions

  • the present invention relates an improved soft touch coating composition, in particular to a soft touch coating composition having improved properties in terms of maintenance of their features over the time
  • soft touch coating products are desired by the consumers because of their pleasant tactile feeling, non-slip grip and ergonomic comfort.
  • the coating has to function constantly over the desired service time demanded in the market where daily interaction between the users and the coating surfaces occur, such as in the consumer electronic goods and automobile interior surfaces.
  • the coating Apart from robust adhesion to the coated surface, the coating itself has to perform well when exposed to common chemicals, such as human sweat, various cosmetics, including sun screens, food items, such as coffee and ketchups.
  • a di-functional polyol binder is normally required in order to achieve the desired tactile feeling for the coating surface.
  • polyester-based diols or polyols are used as binders. These types of diols normally react relatively slow at the desired cure temperature. In order to process the coating composition effectively, it has to dry within an acceptable period of time.
  • a suitable catalyst is added to promote the reaction between the polyol and the polyfunctional isocyanates. Such catalysts normally cause rapid reaction between the binder and the cross linker immediately after the two components are mixed.
  • Soft touch coatings known in the prior arts do normally provide most of the desired performance characteristics when the coating is freshly applied under a control application environment.
  • the resulting soft touch coating products often experience unexpected random failures in various physical property performances.
  • Most commonly seen performance deteriorations are adhesion loss and stickiness already after six months of use.
  • Chemical resistance properties are normally also reduced but are less apparent than adhesion loss or becoming sticky.
  • a deterioration of the coating performances can be expected when the coating is exposed to harsh environments or demanding usage conditions.
  • the main aim of the present invention is to provide a soft touch coating composition, and in particular a polyurethane-based soft touch coating composition, which enables the above problems to be overcome.
  • an object of the present invention is to provide a soft touch coating composition with improved resistance to common chemicals, such as human sweat, cosmetics, food items, beverages and similar.
  • Another object of the present invention is to provide a soft touch coating composition with improved resistance to harsh environments.
  • Yet another object of the present invention is to provide a soft touch coating composition that does not have performance deteriorations such as adhesion loss and stickiness after a relatively short period of use
  • Last but not least object of the present invention is to provide a soft touch coating composition which is highly reliable, relatively simple to produce and with competitive costs.
  • the present invention relates to a polyurethane soft touch coating composition characterized in that it comprises the reaction product of:
  • binders most commonly used are normal hydrolysable polyesters and they are extremely susceptible to poor performance.
  • Non-hydrolysable binders such as polyether or polycarbonate diols have been found to provide stable performance. Polyesters where the ester linkage is protected from hydrolysis with structures to provide steric hindrance have been also found to be effective.
  • the polyurethane soft touch coating composition according to the invention is not able to scratch off after six weeks aging test with artificial sweat under standard conditions.
  • the scratch test after six weeks aging with artificial sweat under standard conditions is the one reported below under the heading STAND ARS TEST CONDITIONS.
  • compounds usable as binders A for the production of the soft touch coating composition of the invention are non-hydrolysable binders such as polyether, polycarbonate or polyester diols where the ester linkage is protected from hydrolysis with structures to provide steric hindrance.
  • binders may in each case be used individually or in combination with one another.
  • Any desired organic polyisocyanates, preferably diisocyanates may be used, individually or in combination, as component B for the production of the soft touch coating composition of the invention.
  • the polyisocyanates may, for example, be of an aromatic, aliphatic and/or cycloaliphatic nature and have a molecular weight of preferably 126 - 500. These may also comprise diisocyanates containing ether or ester groups.
  • diisocyanates examples include trimethylene diisocyanate, tetramethylene diisocyanate, pentamethylene diisocyanate, hexamethylene diisocyanate, propylene diisocyanate, ethylene diisocyanate, 2,3- dimethylethylene diisocyanate, 1-methyltrimethylene diisocyanate, 1,3-cyclopentylene diisocyanate, 1,4-cyclohexylene diisocyanate, 1,2-cyclohexylene diisocyanate, 1,3-phenylene diisocyanate, 1,4-phenylene diisocyanate, 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, 4,4-diisocyanatodiphenylether, 1,5- dibutylpentamethylene diisocyanate, 2,3- bis(8-isocyanatooctyl)-4-octyl-5- hexylcyclohexane, 3-iso
  • the polyurethane soft touch coating composition of the present invention may contain conventional coating additives.
  • Examples of conventional coating additives are matting agents, levelling agents, rheological agents, such as highly disperse silica, polymeric urea compounds or layered silicates, thickeners, defoamers, wetting agents, anticratering agents, dispersants, UV stabilizers, light stabilizers and catalysts.
  • the additives are used in conventional amounts known to the person skilled in the art, for example, of 0.1 to 5 wt.%, relative to the solids content of the coating composition.
  • Conventional coating solvents may also be present in the preparation of the soft-touch coating compositions of the invention.
  • Polyol A Desmophen 1652 polyol, Bayer Science Material
  • Polyol B T5652 polyol, Asahi Kasei;
  • Polyol C Desmophen 670BA polyol, Bayer Science Material
  • Polyol D SY-951 polyol, DSM;
  • Polyol E PolyTHF650 polyol, BASF;
  • Polyol F PE6003 polyol, Human Chemicals co.
  • Tinuvin 1130, CIBA Tinuvin 1130, CIBA.
  • Tinuvin 292, CIBA Tinuvin 292, CIBA.
  • formulation B was prepared by mixing 25.82 parts b.w. Desmodur N-75 with 37.09 parts b.w. of Butyl Acetate and 37.09 parts b.w. of Xylene Vehicle Solvents.
  • the damp heat cycle was the following:
  • Formulation A-I to A-III which do not pass the test, are based on conventional normal hydrolysable polyesters since Desmophen 1652 (Formulation A-I) is a linear polyester and Desmophen 670BA is a slightly branched polyester. By using this latter in combination with a polycarbonate polyol (T5652 polyol - see formulation A-II) the situation is slightly improved, but since the hydrolysable polyesters is the predominant binder the test was not passed.
  • the polyurethane soft touch coating composition of the invention can withstand exposure to relatively harsh environment maintaining robust long term physical performance.
  • the polyurethane soft touch coating composition according to the present invention may advantageously be used for coating manufatured articles.
  • Manufactured article such as consumer electronic articles or an automobile interior surfaces, in which at least a portion of their surface is coated with a polyurethane soft touch coating composition as described herein are also part of the present invention.

Abstract

A polyurethane softtouch coating composition characterized in that it comprises the reaction product of: A) a non-hydrolysable polyol binder; and B) an organic polyisocianate. The polyurethane softtouch coating composition has an improved resistance to harsh environments and in particular it is not able to scratch off after six weeks aging test with artificial sweat under standard conditions.

Description

SOFT TOUCH COATING COMPOSITION
DESCRIPTION
The present invention relates an improved soft touch coating composition, in particular to a soft touch coating composition having improved properties in terms of maintenance of their features over the time
As it is known, soft touch coating products are desired by the consumers because of their pleasant tactile feeling, non-slip grip and ergonomic comfort. In addition to its unique tactile touch property, the coating has to function constantly over the desired service time demanded in the market where daily interaction between the users and the coating surfaces occur, such as in the consumer electronic goods and automobile interior surfaces. Apart from robust adhesion to the coated surface, the coating itself has to perform well when exposed to common chemicals, such as human sweat, various cosmetics, including sun screens, food items, such as coffee and ketchups.
In case of Polyurethane-based soft touch coatings, a di-functional polyol binder is normally required in order to achieve the desired tactile feeling for the coating surface. In most cases, polyester-based diols or polyols are used as binders. These types of diols normally react relatively slow at the desired cure temperature. In order to process the coating composition effectively, it has to dry within an acceptable period of time. A suitable catalyst is added to promote the reaction between the polyol and the polyfunctional isocyanates. Such catalysts normally cause rapid reaction between the binder and the cross linker immediately after the two components are mixed.
Soft touch coatings known in the prior arts do normally provide most of the desired performance characteristics when the coating is freshly applied under a control application environment. However, when applied in a mass production environment, where process parameters are not precisely controlled, the resulting soft touch coating products often experience unexpected random failures in various physical property performances. Most commonly seen performance deteriorations are adhesion loss and stickiness already after six months of use. Chemical resistance properties are normally also reduced but are less apparent than adhesion loss or becoming sticky. In particular, a deterioration of the coating performances can be expected when the coating is exposed to harsh environments or demanding usage conditions.
The main aim of the present invention is to provide a soft touch coating composition, and in particular a polyurethane-based soft touch coating composition, which enables the above problems to be overcome. Within this aim, an object of the present invention is to provide a soft touch coating composition with improved resistance to common chemicals, such as human sweat, cosmetics, food items, beverages and similar.
Another object of the present invention is to provide a soft touch coating composition with improved resistance to harsh environments.
Yet another object of the present invention is to provide a soft touch coating composition that does not have performance deteriorations such as adhesion loss and stickiness after a relatively short period of use
Last but not least object of the present invention is to provide a soft touch coating composition which is highly reliable, relatively simple to produce and with competitive costs.
It has now been surprisingly found that by appropriately selecting the binder (i.e. the polyol) used in the preparation of soft touch coating compositions, it is possible to obtain a soft touch coating composition having robust long term physical performance under demanding usage conditions.
Thus, the present invention relates to a polyurethane soft touch coating composition characterized in that it comprises the reaction product of:
A) a non-hydrolysable polyol binder; and
B) an organic polyisocianate.
In fact, it has been found that the nature of the di-functional binders determines the performance of the soft touch coating when it is exposed to harsh environments under extended period of time.
The binders most commonly used are normal hydrolysable polyesters and they are extremely susceptible to poor performance. Non-hydrolysable binders such as polyether or polycarbonate diols have been found to provide stable performance. Polyesters where the ester linkage is protected from hydrolysis with structures to provide steric hindrance have been also found to be effective.
As better shown in the examples below, the polyurethane soft touch coating composition according to the invention is not able to scratch off after six weeks aging test with artificial sweat under standard conditions.
For the purposes of the present invention, the scratch test after six weeks aging with artificial sweat under standard conditions is the one reported below under the heading STAND ARS TEST CONDITIONS.
Preferably, compounds usable as binders A for the production of the soft touch coating composition of the invention are non-hydrolysable binders such as polyether, polycarbonate or polyester diols where the ester linkage is protected from hydrolysis with structures to provide steric hindrance. Such binders may in each case be used individually or in combination with one another.
Any desired organic polyisocyanates, preferably diisocyanates may be used, individually or in combination, as component B for the production of the soft touch coating composition of the invention.
The polyisocyanates may, for example, be of an aromatic, aliphatic and/or cycloaliphatic nature and have a molecular weight of preferably 126 - 500. These may also comprise diisocyanates containing ether or ester groups. Examples of suitable diisocyanates are trimethylene diisocyanate, tetramethylene diisocyanate, pentamethylene diisocyanate, hexamethylene diisocyanate, propylene diisocyanate, ethylene diisocyanate, 2,3- dimethylethylene diisocyanate, 1-methyltrimethylene diisocyanate, 1,3-cyclopentylene diisocyanate, 1,4-cyclohexylene diisocyanate, 1,2-cyclohexylene diisocyanate, 1,3-phenylene diisocyanate, 1,4-phenylene diisocyanate, 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, 4,4-diisocyanatodiphenylether, 1,5- dibutylpentamethylene diisocyanate, 2,3- bis(8-isocyanatooctyl)-4-octyl-5- hexylcyclohexane, 3-isocyanatomethyl-l-methylcyclohexyl isocyanate and/or 2,6- diisocyanatomethyl caproate.
In principle, the components A and B are reacted in the manner known to the person skilled in the art. Details on the condition used are given in the examples below.
In addition to the components A and B, the polyurethane soft touch coating composition of the present invention may contain conventional coating additives.
Examples of conventional coating additives are matting agents, levelling agents, rheological agents, such as highly disperse silica, polymeric urea compounds or layered silicates, thickeners, defoamers, wetting agents, anticratering agents, dispersants, UV stabilizers, light stabilizers and catalysts. The additives are used in conventional amounts known to the person skilled in the art, for example, of 0.1 to 5 wt.%, relative to the solids content of the coating composition.
Conventional coating solvents may also be present in the preparation of the soft-touch coating compositions of the invention.
EXAMPLES
The following compounds were used in the preparation of comparison and inventive polyurethane soft touch coating compositions.
Polyols
Polyol A: Desmophen 1652 polyol, Bayer Science Material; Polyol B: T5652 polyol, Asahi Kasei;
Polyol C: Desmophen 670BA polyol, Bayer Science Material;
Polyol D: SY-951 polyol, DSM;
Polyol E: PolyTHF650 polyol, BASF;
Polyol F: PE6003 polyol, Human Chemicals co.
Polyisocyanates
Desmodur N-75, Bayer Science Material.
Matting Agents
TS100 matting agent, Evonik Deggusa;
OK520 matting agent, Evonik Deggusa.
Flow Control Agents
Aerosil R974.
Wax
ZA-07 wax, Gifu-Shellac.
Levelling Agents
BYK370 levelling agent, BYK Chemie;
BYK103 levelling agent, BYK Chemie
UV Adsorber
Tinuvin 1130, CIBA.
Light Stabilizer
Tinuvin 292, CIBA.
COMPARATIVE EXAMPLES I-III AND EXAMPLE IV- V.
In the following Table 1 the weight ratios of the compounds used for the preparation of formulation A are reported.
Figure imgf000005_0001
Table 1 - Formulation A {continued)
I II III IV V
(comp.) (comp.) (comp.) (invention) (invention)
Flow Control Agent 1.54
Wax 6.00 6.01 5.95
Drier/Catalyst
1.00
10% Zinc Octoate
Drier/Catalyst
10% DBTL in 1.68 2.49 2.49 2.61 2.49 Butyl Acetate
Levelling Agent BYK 370 0.98 0.98 1.05 0.98
Levelling Agent BYK 103 3.99
UV Adsorber 1.00
Light Stabilizer 0.80
Vehicle Solvent:
Butyl Acetate 14.82 19.54 19.56 28.59 22.57
Methoxy Propyl Acetate 5.99 9.97 9.98 10.46 9.98
Texanol 10.28
Xylene 3.79 7.96 7.97 8.37 7.97
Total 100.00 100.00 100.00 100.00 100.00
For all examples, formulation B was prepared by mixing 25.82 parts b.w. Desmodur N-75 with 37.09 parts b.w. of Butyl Acetate and 37.09 parts b.w. of Xylene Vehicle Solvents.
Then, 50 parts b.w. of each of Formulations A-I to A-V were mixed with formulation B according to the amounts given in Table 2 to prepare a polyurethane coating composition.
Figure imgf000006_0001
In the examples, after thoroughly mixing formulation A and formulation B together, the mixture composition was immediately sprayed and subsequently cured at temperature of 80 °C for 40 min. The cured coating was then covered with artificial sweat solution at pH 2.60 and tested with damp heat cycles for hydrolysis property. The test conditions and test results are as shown below.
STAND ARS TEST CONDITIONS.
Preparation of artificial sweat:
Material used: 1.00 ± 0.01 g of urea (Pro Analysis quality), 5.00 ± 0.01 g of sodium Chloride (Analytical quality) and 1.14 ± 0.02 g DL-lactic acid (>88 %, Analytical quality).
Preparation procedure:
1) The materials mentioned above were added to 900 ml DI water. The solution was stirred until all the added reagents completely dissolved;
2) After calibration, a pH-meter was attached to the solvent and the pH value was adjusted to 2.60 ± O. lOusing dilute ammonia solution (1 %);
3) A further amount of DI water was added to adjust the volume of solution to 1000 ml.
Damp heat cycle:
The damp heat cycle was the following:
25 °C with 95% relative humidity (9 hours);
Temperature increase from 25 °C to 55 °C (3 hours);
55 °C with 95% relative humidity (9 hours).
Scratch resistance test
A Scratch Resistant test was carried out on the above-prepared coating compositions after a continued period in a humidity chamber and covered with artificial sweat. The results are reported in Table 3.
Figure imgf000007_0001
The above results shows the surprising effects of the polyurethane soft touch coating composition according to the invention.
Formulation A-I to A-III, which do not pass the test, are based on conventional normal hydrolysable polyesters since Desmophen 1652 (Formulation A-I) is a linear polyester and Desmophen 670BA is a slightly branched polyester. By using this latter in combination with a polycarbonate polyol (T5652 polyol - see formulation A-II) the situation is slightly improved, but since the hydrolysable polyesters is the predominant binder the test was not passed.
Conversely, when using a polyether polyol (PolyTHF650 - formulation A-IV) or when using a highly modified, sterically hindered polyester (PE6003 - formulation A-V) the test was successfully passed.
It has been seen how the polyurethane soft touch coating composition according to the invention makes it possible to fully achieve the set aim and objects.
As shown by the resistance test carried out on both inventive and comparative composition, the polyurethane soft touch coating composition of the invention can withstand exposure to relatively harsh environment maintaining robust long term physical performance.
The polyurethane soft touch coating composition according to the present invention may advantageously be used for coating manufatured articles.
Manufactured article, such as consumer electronic articles or an automobile interior surfaces, in which at least a portion of their surface is coated with a polyurethane soft touch coating composition as described herein are also part of the present invention.
On the basis of the foregoing description, other characteristics, modifications or improvements are possible and evident to the average person skilled in the art. These characteristics, modifications and improvements must therefore be considered part of the present invention.

Claims

1. A polyurethane soft touch coating composition characterized in that it comprises the reaction product of:
A) a formulation comprising a non-hydrolysable polyol binder; and
B) a formulation comprising an organic polyisocyanate.
2. The polyurethane soft touch coating composition according to claim 1, characterized in that said composition is not able to scratch off after six weeks aging test with artificial sweat under standard conditions.
3. The polyurethane soft touch coating composition according to claim 1 or 2, characterized in that said non-hydrolysable polyol binder is selected form the group consisting of non-hydrolysable polyether, polycarbonate or polyester diols where the ester linkage is protected from hydrolysis with structures to provide steric hindrance.
4. The polyurethane soft touch coating composition according to one or more of the preceding claims, characterized in that said organic polyisocyanate is an aromatic, aliphatic and/or cycloaliphatic polyisocyanate.
5. The polyurethane soft touch coating composition according to claim 4, characterized in that said organic polyisocianate is selected from: trimethylene diisocyanate, tetramethylene diisocyanate, pentamethylene diisocyanate, hexamethylene diisocyanate, propylene diisocyanate, ethylene diisocyanate, 2,3-dimethylethylene diisocyanate, 1-methyltrimethylene diisocyanate, 1,3-cyclopentylene diisocyanate, 1,4-cyclohexylene diisocyanate, 1,2-cyclohexylene diisocyanate, 1,3-phenylene diisocyanate, 1,4-phenylene diisocyanate, 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, 4,4-diisocyanatodiphenylether, 1,5- dibutylpentamethylene diisocyanate, 2,3-bis(8-isocyanatooctyl)-4-octyl-5-hexylcyclohexane, 3-isocyanatomethyl-l-methyl- cyclohexyl isocyanate and/or 2,6- diisocyanatom ethyl caproate.
6. The polyurethane soft touch coating composition according to one or more of the preceding claims chracaterized in that said formulation A comprise one or more of the following: matting agents, levelling agents, rheological agents, thickeners, defoamers, wetting agents, anticratering agents, dispersants, UV stabilizers, light stabilizers and catalysts.
7. Use of the polyurethane soft touch coating composition according to one or more of the preceding claims for coating manufatured articles.
8. A manufactured article, such as consumer electronic article or an automobile interior surface, characterized in that at least a portion of its surface is coated with a polyurethane soft touch coating composition according to one or more of claims 1 to 6.
PCT/EP2011/074270 2010-12-30 2011-12-29 Soft touch coating composition WO2012089827A1 (en)

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WO2016042143A1 (en) * 2014-09-19 2016-03-24 Jotun A/S Composition
US9566474B2 (en) 2013-03-15 2017-02-14 Nike, Inc. Golf ball with soft coating and hard cover
CN109476812A (en) * 2016-07-28 2019-03-15 科思创德国股份有限公司 Low hardness polyurethane dispersion
JP2020508848A (en) * 2017-02-13 2020-03-26 タクタス テクノロジー, インコーポレイテッドTactus Technology, Inc. Method of forming cast elastomer
EP3828217A1 (en) 2016-03-02 2021-06-02 Arkema France Dual cure soft touch coatings
CN113667082A (en) * 2021-07-26 2021-11-19 清远慧谷新材料技术有限公司 Soft touch hydroxyl polyurethane dispersion and preparation method thereof
US11530333B2 (en) 2016-12-26 2022-12-20 Akzo Nobel Coatings International B.V. Coating composition system, the preparation method, and the use thereof
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US11111410B2 (en) 2016-03-02 2021-09-07 Arkema France Dual cure soft touch coatings
EP3828217A1 (en) 2016-03-02 2021-06-02 Arkema France Dual cure soft touch coatings
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