An adhesive agent produced by crosslinking an adhesive agent composition containing a polyester resin (i) having a structural portion derived from a polycarboxylic acid compound (a) and a structural portion derived from a polyol component (b), wherein the polyester resin (i) contains a structural portion derived from at least one selected from the group consisting of a dimer acid compound, a sebacic acid compound, and a dimer diol in a proportion of not less than 60 wt. % based on the weight of the polyester resin (i), wherein the polyol component (b) includes a glycol (b1) having an even carbon number (excluding the dimer diol), wherein the polyester resin (i) has an ester group concentration of not less than 2 mmol/g. The adhesive agent has an adhesive force (α) of not less than 1 N/25 mm as measured under predetermined conditions.

A hot melt adhesive (HMA), which is solid at room temperature, comprises the reaction product of 5 to 25% by weight of an isocyanate component having an NCO content of from about 20 to about 50% by weight, 75 to 85% by weight of a polyester, and 1 to 10% by weight of a hydroxy-polymer having an OH number of from about 40 to about 50. A method of forming the adhesive comprises the step of combining the isocyanate component, polyester, and hydroxy-polymer to form the adhesive. The adhesive can be used for various purposes, such as for forming an adhesive layer which adhesively couples surfaces together.

A hot melt adhesive (HMA), which is solid at room temperature, comprises the reaction product of 5 to 25% by weight of an isocyanate component having an NCO content of from about 20 to about 50% by weight, 75 to 85% by weight of a polyester, and 1 to 10% by weight of a hydroxy-polymer having an OH number of from about 40 to about 50. A method of forming the adhesive comprises the step of combining the isocyanate component, polyester, and hydroxy-polymer to form the adhesive. The adhesive can be used for various purposes, such as for forming an adhesive layer which adhesively couples surfaces together.

The present invention relates to a polyurethane which is the reaction product of a polyisocyanate and polyester, wherein said polyester is formed from a dimer fatty acid, a C.sub.2 to C.sub.4 diol, and a C.sub.8 to C.sub.16 dicarboxylic acid or C.sub.6 to C.sub.12 lactide. The inventions also relates to a polyester for use in forming the polyurethane of the first aspect, said polyester formed from a dimer fatty acid, a C.sub.2 to C.sub.4 diol, and a C.sub.8 to C.sub.16 dicarboxylic acid or C.sub.6 to C.sub.12 lactide.

The present invention relates to a polyurethane which is the reaction product of a polyisocyanate and polyester, wherein said polyester is formed from a dimer fatty acid, a C.sub.2 to C.sub.4 diol, and a C.sub.8 to C.sub.16 dicarboxylic acid or C.sub.6 to C.sub.12 lactide. The inventions also relates to a polyester for use in forming the polyurethane of the first aspect, said polyester formed from a dimer fatty acid, a C.sub.2 to C.sub.4 diol, and a C.sub.8 to C.sub.16 dicarboxylic acid or C.sub.6 to C.sub.12 lactide.

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 still free NCO groups in the material including the fusible polymer.

The invention concerns a two-component polyurethane composition including a polyol component K1 and a polyisocyanate component K2, the polyol component K1 including castor oil A1 and 1,2,3-propane triol A2, and the polyisocyanate component K2 including at least one aromatic polyisocyanate B1, the ratio in weight percent of (A1/A2) being between 4 and 50 and the ratio of all NCO groups of the aromatic polyisocyanates B1 to all the OH groups totaling (A1+A2)=1.15:1-85:1, and the total of all the OH groups of (A1+A2) being >93% of the total of all the OH groups of the two-component polyurethane composition, characterized by controllable hydrolytic degradability.

The invention concerns a two-component polyurethane composition including a polyol component K1 and a polyisocyanate component K2, the polyol component K1 including castor oil A1 and 1,2,3-propane triol A2, and the polyisocyanate component K2 including at least one aromatic polyisocyanate B1, the ratio in weight percent of (A1/A2) being between 4 and 50 and the ratio of all NCO groups of the aromatic polyisocyanates B1 to all the OH groups totaling (A1+A2)=1.15:1-85:1, and the total of all the OH groups of (A1+A2) being >93% of the total of all the OH groups of the two-component polyurethane composition, characterized by controllable hydrolytic degradability.

Provided herein are novel and improved weight coating systems suitable for use with pipes, particularly pipes that are submerged in liquid, such as water, in environments including oceans, seas, marshes, lakes and rivers. The novel coating systems provided herein comprise an aggregate and a polyurethane binder, wherein the polyurethane binder is a two -component composition comprising an isocyanate component and an iso-cyanate-reactive component. The coating systems provided have increased durability, as well as flexibility allowing for efficiencies related to transportation, storage, use and resistance to corrosive effects. Furthermore, the coating systems are cost effective and have minimal or zero impact on the environments in which they are utilized.

A method for reducing coefficient of friction of a laminate comprising a polyurethane adhesive is provided. The method comprises providing the polyurethane adhesive; and adhering at least two substrates with the polyurethane adhesive to form a laminate, wherein the polyurethane adhesive is formed by reacting (A) an isocyanate component comprising a prepolymer derived from the reaction of a diisocyanate, a polyethylene glycol and optionally an additional polyol; with (B) a polyol component. The method can achieve minimized COF and viscosity, while retaining other performance properties such as bond strength, heat seal strength and boil in bag resistance. A composition for preparing the adhesive, a laminate product prepared with said composition as well the method for preparing the laminate product are also provided.