A polymerizable composition for an optical material containing two or more different monomers for an optical material, and a polymerization catalyst, in which at least one of the two or more different monomers for an optical material is an isocyanate compound containing an aromatic ring, a content of the polymerization catalyst with respect to a total of 100 parts by mass of the two or more different monomers for an optical material is from 0.010 parts by mass to 0.50 parts by mass, and the viscosity measured by a B-type viscometer at 25° C. and 60 rpm is from 10 mPa.Math.s to 1,000 mPa.Math.s.

In a xylylene diisocyanate-containing container including a xylylene diisocyanate and a container accommodating the xylylene diisocyanate, a resin layer is provided on an inner surface of a container.

A xylylenediisocyanate composition including xylylenediisocyanate and a compound represented by Chemical Formula (1) below, wherein 0.6 ppm or more and 60 ppm or less of the compound represented by Chemical Formula (1) below is contained: ##STR00001##

Display modules typically incorporate a transparent hard material such as glass on the outside of the module in order to better protect the display stack from scratches, dents, and other mechanical deformations. However, as displays move to novel form factors such as bendable, foldable, and reliable display modules, these transparent hard materials (e.g., glass) may not be used due to their limited flexibility. Therefore, it is desirable that replacement materials be sufficiently flexible while maintaining the desirable optical (e.g., >90% transmission and low yellow index) and mechanical properties (e.g., pencil hardness>H) that comparable glass hard materials offer.

A polymerizable composition for an optical material includes (A) one or more isocyanate compounds selected from aliphatic isocyanate compounds and alicyclic isocyanate compounds, (B) an active hydrogen compound having two or more functional groups, and (C) a photochromic compound.

A polythiol composition according to the present invention includes a polythiol compound (A) having three or more mercapto groups and a nitrogen-containing compound (B) in which one of a mercapto group of the polythiol compound (A) is replaced with a group represented by the following formula (a) and other one of a mercapto group of the polythiol compound (A) is replaced with a hydroxyl group, in which the peak area of the nitrogen-containing compound (B) is equal to or less than 3.0 with respect to the peak area of 100 of the polythiol compound (A) in a high performance liquid chromatography measurement. ##STR00001##

The polymerizable composition of the present invention contains (A) an alicyclic isocyanate compound (a1) having two or more functional groups and/or an aliphatic isocyanate compound (a2) having two or more functional groups, (B) a thiol compound having one or more sulfide bonds and/or one or more ester bonds and having two or more functional groups, and (C) an imidazole-based curing catalyst, in which the amount of the imidazole-based curing catalyst (C) is 5 ppm to 3,000 ppm with respect to the total amount of the isocyanate compound (A) and the thiol compound (B).

The invention relates to a non-aqueous coating composition comprising a. a polyisocyanate, b. a polyol having an average functionality of more than 3 hydroxyl groups per molecule, c. a metal based curing catalyst for the addition reaction of isocyanate groups and hydroxyl groups, and d. a mercapto carboxylic acid, wherein the coating composition does not contain a carboxylic acid wherein the carbonyl group of the carboxylic acid is in conjugation with π-electron system.

The present invention relates to an adhesive system, comprising an adhesion promoter composition, containing at least one mercaptosilane, at least one polysilane, at least one transition metal complex comprising substantially only monodentate ligands, and at least one nonalcoholic solvent, and an adhesive, wherein the adhesive, within an hour after application and storage at 23° C. and 50% relative air humidity, has a tensile shear strength of at least 3 MPa, as measured according to ISO 4587, and/or, within an hour after application and storage at 23° C. and 50% relative air humidity, has at least 50%, preferably at least 60%, of the tensile shear strength achievable after application and storage for 7 days at 23° C. and 50% relative air humidity, as measured according to ISO 4587. The adhesive system according to the invention is suited, for example, for bonding glass panes in transport means and also builds up strength very quickly at low temperatures. The present invention further relates to an adhesion promoter system having a liquid container comprising a manually actuable output apparatus, and an adhesion promoter composition, as disclosed above.

The present invention is a method of curing an adhesive composition positioned at least partially under a light-absorbing layer. The method includes providing an adhesive composition, positioning the light-absorbing layer over a surface of the adhesive composition such that there is an exposed area of the adhesive composition and a covered area of the adhesive composition and irradiating the exposed area of the adhesive composition and the covered area of the adhesive composition at the surface at a dosage of between about 100 mJ/cm.sup.2 and about 10,000 mJ/cm.sup.2. The adhesive composition includes a solute (meth)acryolyl oligomer having a molecular weight of 4 to 30 k and a Tg of less than about 20° C., a diluents monomer component and a photoinitiator.