A method of forming a three-dimensional object (e.g. comprised of polyurethane, polyurea, or copolymer thereof) is carried out by: (a) providing a carrier and an optically transparent member having a build surface, the carrier and the build surface defining a build region therebetween; (b) filling the build region with a polymerizable liquid, the polymerizable liquid comprising a mixture of: (i) a light polymerizable liquid first component, and (ii) a second solidifiable component that is different from the first component; (c) irradiating the build region with light through the optically transparent member to form a solid blocked polymer scaffold and advancing the carrier away from the build surface to form a three-dimensional intermediate having the same shape as, or a shape to be imparted to, the three-dimensional object, with the intermediate containing the second solidifiable component; and then (d) contacting the three-dimensional intermediate to water to form the three-dimensional object.

Disclosed are compositions comprising a liquid carrier, a polysulfide rubber curing agent, a metal cation, and an ionic liquid. Also disclosed are methods for curing a surface of an uncured polysulfide rubber. These methods involve applying the disclosed compositions to the surface of the uncured polysulfide rubber.

Disclosed are compositions comprising a liquid carrier, a polysulfide rubber curing agent, a metal cation, and an ionic liquid. Also disclosed are methods for curing a surface of an uncured polysulfide rubber. These methods involve applying the disclosed compositions to the surface of the uncured polysulfide rubber.

Disclosed is a reaction mixture for the manufacturing of a polyurethane foam, which mixture can be obtained by reacting a polyfunctional isocyanate with an isocyanate-reactive compound, in the presence of a scavenger and at least one catalyst; and curing such reaction mixture enables providing a foam with reduced aldehyde emissions particularly useful in means of transport, such as interior part of cars.

Disclosed is a reaction mixture for the manufacturing of a polyurethane foam, which mixture can be obtained by reacting a polyfunctional isocyanate with an isocyanate-reactive compound, in the presence of a scavenger and at least one catalyst; and curing such reaction mixture enables providing a foam with reduced aldehyde emissions particularly useful in means of transport, such as interior part of cars.

The present invention relates to two-component clear-coat systems comprising polyaspartic esters having primary amino groups and small amounts of dialkyl fumarates, to a process for the production thereof, and to the use thereof in the production of coatings for vehicle repair applications and to substrates coated therewith.

A coating composition containing a. polyvinyl chloride b. one or more compounds of formula (I) ##STR00001## in which R.sup.1a and R.sup.1b are C.sub.7- to C.sub.12-alkyl c. one or more compounds having plasticizing properties selected from adipates comprising C.sub.1- to C.sub.6-radicals, glutarates comprising C.sub.1- to C.sub.6-radicals, sebacates comprising C.sub.2- to C.sub.6-radicals, dibenzoates, monobenzoates comprising a C.sub.5- to C.sub.10-alkyl radical or a benzyl radical, compounds of formula (II), compounds of formula (III), phenyl esters of pentadecylsulfonic acid, cresyl esters of pentadecylsulfonic acid, terephthalates, levulinic esters, isosorbitol valerate, trimellitates and 2,2,4-trimethyl-1-3-pentanediol-diisobutyrate, d. one or more compounds of general formula (IV) ##STR00002##

A coating composition containing a. polyvinyl chloride b. one or more compounds of formula (I) ##STR00001## in which R.sup.1a and R.sup.1b are C.sub.7- to C.sub.12-alkyl c. one or more compounds having plasticizing properties selected from adipates comprising C.sub.1- to C.sub.6-radicals, glutarates comprising C.sub.1- to C.sub.6-radicals, sebacates comprising C.sub.2- to C.sub.6-radicals, dibenzoates, monobenzoates comprising a C.sub.5- to C.sub.10-alkyl radical or a benzyl radical, compounds of formula (II), compounds of formula (III), phenyl esters of pentadecylsulfonic acid, cresyl esters of pentadecylsulfonic acid, terephthalates, levulinic esters, isosorbitol valerate, trimellitates and 2,2,4-trimethyl-1-3-pentanediol-diisobutyrate, d. one or more compounds of general formula (IV) ##STR00002##

The present disclosure is directed to peelable, heat-sealable lidding films for containers of diverse polymer compositions storing various products such as foodstuffs and pharmaceuticals. The lidding films disclosed herein can be heat-sealed to crystalline polyester trays (CPET), easily peeled, and contain improved antifogging performance by incorporating a non-migratory antifogging additive into the heat sealable layer of the film without deteriorating seal strengths.

The present document describes a polyamide hot-melt resin having a chemical structure consisting of dimerized fatty acids and diamines, loaded with an active ingredient. The dimerized fatty acids may have 12 to 24 carbons and the diamines may have 2 to 14 carbons. The amine residual functional groups and acid residual functional groups within the polyamide hot-melt resin may have a [NH.sub.2]/[COOH] molar ratio below 5, and the active ingredient may be incorporated in quantities of between about 0.01 and about 55% by weight of weight of the resin. The present document also describes items molded from the polyamide hot-melt resins, and processes of preparing the polyamide hot-melt resins.