The present invention relates to a process for the preparation of a coating, a coated substrate, an adhesive, film or sheet, which process comprises the application of a formulation mixture containing a reactive system onto a substrate. According to the invention a low VOC formulation mixture is used, wherein more than 40% of the carbon in the combined amount of the formulation mixture is modern carbon according to ASTM D6866.

Provided is an aqueous composition comprising dispersed particles that comprise a polyurethane, wherein said polyurethane is a reaction product of a group of reactants (GR1), wherein GR1 comprises one or more aromatic polyisocyanates and, a polyol component, wherein said polyol component comprises (a) 50% to 99% by weight, based on the weight of said polyol component, one or more polyester polyols, (b) 0.1% to 10% by weight, based on the weight of said polyol component, one or more diols having a hydrophilic side chain, and (c) 0.9% to 40% by weight, based on the weight of said polyol component, one or more polyols different from (a) and (b). Also provided is a method of bonding a metal foil to a polymer film using such an aqueous composition.

A radiation curable polyurethane resin includes an ionic group, a polyalkylene oxide in a side chain thereof, and a (meth)acrylate or (meth)acrylamide having a hydroxyl functional group. The polyurethane resin is obtainable by reacting a polyester polyol, a polyether diol, a polyol containing an ionic group, a (meth)acrylate or (meth)acrylamide having a hydroxyl functional group, and a polyisocyanate. The polyester polyol is obtained by reacting a polycarboxylic acid and a polyol. The radiation curable polyurethane resin can be used as binder in an aqueous ink jet ink.

A method for producing an object comprises the step of producing the object by means of an additive manufacturing process from a construction material. The construction material comprises a first polyurethane polymer which has: a weight percentage ratio of O to N of ≥2 to ≤2.5, determined by elementary analysis; a weight percentage ratio of N to C of ≥0.1 to ≤0.25, determined by elementary analysis; a full-width at half maximum of the melting peak of ≤20 K, determined by dynamic differential scanning calorimetry DSC (2.sup.nd heating at heating rate 20 k/min); and a difference between the melting temperature and the recrystallisation temperature of ≥5 K and ≤100 K, determined by dynamic differential scanning calorimetry DSC (2.sup.nd heating) at a heating and cooling rate of 20 K/min.

A medical tubing contains a thermoplastic polyurethane.

The resealable bag has a main body including a resealing layer. The resealable bag is selectively positionable between an open, unsealed position and a closed, sealed position. When the resealable bag is in the closed, sealed position, the resealing layer is in a deformed shape. Advantageously, the resealable bag can be repeatedly rolled and sealed, and unrolled and unsealed, as desired without the use of additional integrated or non-integrated sealing mechanisms.

An embodiment of the present technology is an isocyanate-based adhesive used for a surface-treated crystalline thermoplastic resin base material, the isocyanate-based adhesive having a value represented by (JIS-A hardness)/(strength at break [MPa])×(elongation at break (%))/100 of 2.0 to 70 after being cured by being allowed to stand still under a condition at 23° C. and 50% RH for 3 days, and the crystalline thermoplastic resin base material having a value represented by (δ.sup.d/δ.sup.p+δ.sup.p) of 2.0 to 30.0. δ.sup.p=γ.sup.p−γ.sup.p0 and δ.sup.d=|γ.sup.d−γ.sup.d0|, γ.sup.p0 is a polar term of surface free energy before the surface treatment, γ.sup.p is a polar term of surface free energy after the surface treatment, γ.sup.d0 is a dispersion term of the surface free energy before the surface treatment, and γ.sup.d is a dispersion term of the surface free energy after the surface treatment.

A nonlimiting example method of forming highly spherical carbon nanomaterial-graft-polyurethane (CNM-g-polyurethane) particles may comprising: mixing a mixture comprising: (a) carbon nanomaterial-graft-polyurethane (CNM-g-polyurethane), wherein the CNM-g-polyurethane particles comprises: a polyurethane grafted to a carbon nanomaterial, (b) a carrier fluid that is immiscible with the polyurethane of the CNM-g-polyurethane, optionally (c) a thermoplastic polymer not grafted to a CNM, and optionally (d) an emulsion stabilizer at a temperature greater than a melting point or softening temperature of the polyurethane of the CNM-g-polyurethane and the thermoplastic polymer, when included, and at a shear rate sufficiently high to disperse the CNM-g-polyurethane in the carrier fluid; cooling the mixture to below the melting point or softening temperature to form CNM-g-polyurethane particles; and separating the CNM-g-polyurethane particles from the carrier fluid.

A low-VOC, two-component polyurethane adhesive is provided. The polyurethane adhesive has an A-side that includes an isocyanate and a non-reactive plasticizer, and a B-side that includes an aliphatic polyester polyol, a non-polyester polyol, and a urethane catalyst. The A-side and the B-side are reacted at a volume ratio of 1:1 and formulated at an NCO/OH index within the range of 0.90 to 1.10. The polyurethane adhesive is solvent-free and is particularly suitable for adhering a polymeric membrane to a substrate.

The present embodiments relate to an antifouling article comprising polyurethane and medetomidine, or an enantiomer or salt thereof, from 0.1% by weight of the antifouling article and present in a polymer matrix of the polyurethane.