Patent classifications
C08G18/4808
AMPHIPHILIC SILOXANE POLYURETHANE COATING COMPOSITIONS AND METHODS OF MAKING AND USING THEREOF
The invention relates to a curable amphiphilic siloxane polyurethane coating composition. The invention also relates to methods of making and using the curable amphiphilic siloxane polyurethane coating composition of the invention. The invention also relates to methods for reducing or preventing biofouling of a surface exposed to an aqueous environment comprising the use of the curable amphiphilic siloxane polyurethane coating composition of the invention.
PARTIALLY COATED FILMS AND PACKAGES FORMED FROM SAME
The present invention provides coated films and packages formed from such films. In one aspect, a partially coated film comprises (a) a film having two outer surfaces, wherein a first outer surface is provided by a film layer that comprises from 70 to 100 percent by weight of a polyolefin having a density of 0.860 to 0.965 g/cm.sup.3; and (b) a coating on the first outer surface of the film comprising polyurethane, wherein the coating covers less than 25% of the surface area of the first outer surface of the film and wherein the coated portion of the film exhibits an Elmendorf tear in at least one of the machine direction or cross direction that is at least 20% less than the Elmendorf tear of the uncoated portion in the same direction, with the Elmendorf tear being measured in accordance with ASTM D1922.
NON-IONIC WATER BASED POLYURETHANE AND PREPARATION METHOD AND USE THEREOF
The disclosure provides a non-ionic water based polyurethane, which is prepared from the following components in parts by weight: 120-185 parts of polymeric polyol, 30-40 parts of diisocyanate, 0.3-0.6 parts of antioxidant, 0.1-0.5 parts of organometallic catalyst, 1-3 parts of intramolecular crosslinking agent, 4-6 parts of silicone oil, 2.1-5.5 parts of auxiliary, 1-2 parts of chain extender, and 600-750 parts of water, where the polymeric polyol includes a polyether diol and a polyester diol, and the auxiliary includes a wetting agent, a leveling agent and a defoamer. The non-ionic water based polyurethane provided by the disclosure has excellent water resistance, mechanical properties and compatibility. Moreover, no organic solvent is added, thus, the disclosure results in no secondary pollution, and ensures environmental protection.
Polyurethanes for contact lenses
The present invention provides a poly(ethylene) glycol based polyurethane polymer composition, particularly useful in the production of contact lenses. Generally the reactant mixture used to form the polymer includes a branched chain extender. There is also provided a method of manufacturing a contact lens formed from such a polymer.
Coating composition
The present invention relates to a coating composition, a coating system comprising the coating composition, a coating method and application of the coating system, and a product coated with the coating system. The coating composition comprises: (A) at least one aqueous polyurethane dispersion and/or one aqueous polyacrylate dispersion, wherein the aqueous polyurethane dispersion comprises at least one polyurethane polymer (a), wherein the polyurethane polymer (a) is obtained by a reaction comprising at least one polyurethane prepolymer (a1) and at least one isocyanate-reactive component (a2), wherein the polyurethane prepolymer (a1) is obtained by a reaction comprising the following components: (a1-1) at least one polyisocyanate having an isocyanate functionality of no less than 2, and (a1-2) at least one polyfunctional polyether polyol having a hydroxyl functionality of no less than 3, wherein the polyfunctional polyether polyol has an amount of 1 wt % to 20 wt %, based on the amount of the components for preparing the polyurethane prepolymer being 100 wt %, and (B) at least one crosslinking agent.
Method for applying a material containing a meltable polymer with blocked NCO groups
A method of applying a material comprising a fusible polymer comprises the step of: applying a filament of the at least partly molten material comprising a fusible polymer from a discharge opening of a discharge element to a first substrate. The fusible polymer has the following properties: a melting point (DSC, differential scanning calorimetry; 2nd heating at heating rate 5° C./min) within a range from ≥35° C. to ≤150° C.; a glass transition temperature (DMA, dynamic-mechanical analysis to DIN EN ISO 6721-1:2011) within a range from ≥−70° C. to ≤110° C.;
wherein the filament, during the application process, has an application temperature of ≥100° C. above the melting point of the fusible polymer for ≤20 minutes. There are furthermore blocked NCO groups present in the material comprising the fusible polymer.
WOOD PRESERVATIVES
A method for preserving wood by contacting wood with a composition comprising a polyurethane polymer, non-aqueous solvents, and a wood preservative.
Polyurethane polymer having a hardness of less than or equal to 60 shore A and good abrasion resistance
The present invention relates to a novel thermoplastically processible polyurethane polymer having a hardness of ≤60 Shore A, to compositions containing this polyurethane polymer, to the uses thereof and to articles containing this polyurethane polymer.
Two component polyurethane composition
The present invention relates to a composition comprising a first component containing at least one polyol, and a second component containing at least one polyisocyanate, the composition further comprising at least one aldimine of formula (I). The composition exhibits a long open time and fast curing without odor immissions, wherein a bubble-free, elastic material having a non-tacky surface and good strength, extensibility, elasticity and resistance is produced, which does not tend to problems arising with plasticizer migration.
AZIRIDINYL FUNCTIONAL COMPOUND
The present invention relates to compount (I) comprising at least one functional group A and at least one functional group B, wherein the functional groups A has structural formula A: wherein R.sub.1 is H, R.sub.2, R.sub.3 and R.sub.4 are independently chosen from H, methyl or ethyl, m is 1-6; and the functional groups B has structural formula B: R.sub.5 is H or methyl, X is O or NH, Z′ is a polyalkoxy group or an omega-alkoxy polycaprolacton group, Y′ is a collection of atoms covalently connected in linear or branched configuration n″ is 0 or 1, and m′ is an integer from 1-6; with the proviso that the summed amount of the number of functional groups A and the number of functional groups B in compound (I) is from 2-13; and the compound has a molecular weight in the range from 800-10000 Dalton.
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