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Pooyurethane dispersion in alcohol-water system

A polyurethane dispersion, dispersion technology, applied in the direction of polyurea/polyurethane adhesive, body powder, skin care preparations, etc., can solve the problems of unproposed utilization, etc., and achieve the effect of improving hydrolytic stability

Inactive Publication Date: 2005-07-20
3M INNOVATIVE PROPERTIES CO
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0011] Neither of the techniques discussed above recognizes the importance of molecular weight control through the use of chain stoppers to impart cold seal adhesive properties, nor does it address the use of these materials in cosmetic or pharmaceutical formulations

Method used

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  • Pooyurethane dispersion in alcohol-water system
  • Pooyurethane dispersion in alcohol-water system

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1 to 3

[0104] Examples 1 to 3 show how changing the ethanol-water ratio of the polyurethane dispersion changes the molecular weight, and thus the peel adhesion value.

[0105] The following components were added to a 1 liter reactor to make each batch 600 grams: 120.6 grams (1.09 NCO equiv.) isophorone diisocyanate; 147.6 grams (0.089 OH equiv.) KRATON L-2203 hydrogenated polybutadiene diol (OH Equivalent weight 1660) from Shell Chemical Co., Houston, TX, USA; 296.4 grams (0.291 OH equiv.) TERATHANE 2000 polytetrahydrofurandiol (OH equiv. weight 1020) from E I. du Pont Co., Wilmington, DE, USA ; 6 grams (0.05 OH equivalents) of SURFYNOL 104 surfactant, a diol (OH equivalent weight 113.2) from Air Products, Lehigh Valley, PA, USA; and 24 grams (0.110 equivalents) of the sulfopolyester prepared above Diol A. The opaque mixture was heated to about 80°C with stirring under nitrogen and 0.5 grams of dibutyltin dilaurate catalyst was added. An exothermic reaction occurred and the tempera...

Embodiment 4 to 8

[0110] Examples 4 to 8 show how varying the weight ratio of chain extender to chain stopper affects the molecular weight of the polyurethane dispersion.

[0111] Following the procedure used in Example 1, combine 78.8 g (47.5 meq OH) KRATON L-2203 diol, 157.6 g (154.5 meq OH) TERATHANE 2000 diol, 12.0 g (40 meq OH) sulfonic acid prepared above Base polyester diol B, and 51.5 grams (464.3 meq NCO) of isophorone diisocyanate were added to a 500 mL reactor, heated and stirred to approximately 80°C under nitrogen. About two drops of dioctyltin dilaurate were added and an exothermic reaction occurred to about 87°C. After the reaction had proceeded for approximately 2.5 hours, the mixture was cooled slightly and a 30-gram aliquot (with 22.2 milliequivalents of theoretical unreacted NCO) was charged to ethylenediamine (EDA, 45 grams of 85:15 ethanol to water in water) chain extender) and 2-amino-2-methyl-1-propanol (AMP, chain stopper) in various ratios in 100 mL vials. The mixture...

Embodiment 9 and 10

[0115] Following the procedure used in Example 1, 46.7 g (28.1 meq OH) KRATON L-2203 diol, 93.3 g (91.5 meq OH) TERATHANE 2000 diol, 20.0 g (66.7 meq OH) the sulfonic acid prepared above Base polyester diol B, and 40 grams (360.4 meq NCO) of isophorone diisocyanate were added to a 500 mL reactor, heated and stirred to approximately 80°C under nitrogen. One drop of dioctyltin dilaurate was added and an exothermic reaction occurred to about 82°C. After the reaction had proceeded for approximately 2 hours, the mixture was cooled slightly and a 30-gram aliquot (with 26.1 milliequivalents of theoretical unreacted NCO) was charged to 0.81 grams or 0.65 grams containing 45 grams of 85:15 ethanol and water in water (27 meq) EDA and 0.48 g (5.4 meq) AMP in a 100 mL vial. Homogenize the mixture using an Omni Macro homogenizer.

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Abstract

A polyurethane dispersion and a method of making are provided. The polyurethane dispersion is stable in a mixture of alcohol and water. The dispersion comprises the reaction product of (a) an isocyanate terminated polyurethane prepolymer comprising the reaction product of (i) at least one oligomeric polyactive hydrogen compound insoluble in said alcohol, wherein said polyactive hydrogen compound is an alkyl, aryl, or aralkyl structure optionally substituted by N, O, and S; (ii) at least one polyisocyanate, and (iii) at least one polyactive hydrogen compound soluble in said mixture of alcohol and water; (b) a polyfunctional chain extender; and (c) a monofunctional chain terminator; wherein the equivalent ratio of difunctional chain extender to prepolymer isocyanate is 0.60 to 1.20.

Description

technical field [0001] The present invention relates to a cold seal adhesive composition in the form of a stable polyurethane dispersion in an alcohol-water system. Background technique [0002] Polyurethane is a generic term used to describe polymers prepared by the reaction of polyfunctional isocyanates and polyfunctional alcohols to form urethane linkages. The term "polyurethane" is also used in a more generic sense to represent the reaction product of a polyisocyanate and any polyactive hydrogen compound including polyfunctional alcohols, amines and thiols. Polyurethanes are used in many applications including as elastomers, adhesives, coatings and impregnants. [0003] For coating applications, polyurethane polymers can be dispersed in water by incorporating stabilizing groups on the backbone. Including anionic, cationic and nonionic dispersion stabilizing groups that have been used. Various aqueous polyurethane dispersions have been prepared by those skilled in the ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61L15/16A61K8/00A61K8/02A61K8/06A61K8/30A61K8/34A61K8/37A61K8/39A61K8/41A61K8/42A61K8/46A61K8/49A61K8/72A61K8/81A61K8/85A61K8/86A61K8/87A61Q1/00A61Q1/02A61Q1/04A61Q1/06A61Q1/08A61Q1/10A61Q1/12A61Q3/02A61Q5/00A61Q5/02A61Q5/12A61Q17/00A61Q17/02A61Q17/04A61Q19/00C08G18/08C08G18/10C08G18/12C08G18/42C08G18/46C08G18/66C09J175/04C09J175/12
CPCA61Q1/02C08G18/12C08G18/0861A61Q1/10A61K8/87A61Q1/06A61Q5/02A61Q19/00C08G18/0819A61Q17/02A61Q17/04C08G18/0804A61Q3/02A61Q1/08A61Q5/12C08G18/3228C08G18/2825C08G18/08
Inventor 斯蒂芬·S·坎特纳马修·T·肖尔茨凯文·M·莱万多夫斯基
Owner 3M INNOVATIVE PROPERTIES CO