C08G18/3256

Latent curing agent and curable polyurethane composition
11535694 · 2022-12-27 · ·

A compound of formula (I) having advantageous properties when used as a latent curing agent for compositions containing isocyanate groups, and to compositions containing the compound of formula (I). The compound of formula (I) is odourless, is liquid and has comparatively low viscosity at room temperature and is stable in storage together with isocyanates. It makes possible odourless single-component polyurethane compositions which have good stability in storage, do not produce bubbles when cured in the presence of moisture, and cause no problematic odour emissions, giving a cured elastic material having good mechanical properties, good heat stability, a surprisingly non-adhesive surface and little tendency towards plasticizer migration.

Latent curing agent and curable polyurethane composition
11535694 · 2022-12-27 · ·

A compound of formula (I) having advantageous properties when used as a latent curing agent for compositions containing isocyanate groups, and to compositions containing the compound of formula (I). The compound of formula (I) is odourless, is liquid and has comparatively low viscosity at room temperature and is stable in storage together with isocyanates. It makes possible odourless single-component polyurethane compositions which have good stability in storage, do not produce bubbles when cured in the presence of moisture, and cause no problematic odour emissions, giving a cured elastic material having good mechanical properties, good heat stability, a surprisingly non-adhesive surface and little tendency towards plasticizer migration.

Blocking agent for amines, latent hardeners and polyurethane compositions
11518736 · 2022-12-06 · ·

The use of an aldehyde mixture containing 70 to 95 wt % of aldehydes of formula (I) and 5 to 30 wt % of alkylbenzene compounds not corresponding to formula (I) as a blocking agent for amines results in odorless, especially economically blocked amines, which at room temperature are typically liquid and have a surprisingly low viscosity. Such blocked amines are particularly suitable as latent hardeners in isocyanate-group-containing compositions. Single-component moisture-curing polyurethane compositions formulated therewith are surprisingly stable in storage, can be used for low-emission applications without odor problems and do not trigger any problems with plasticizer migration. Surprisingly, said compositions even have advantages over corresponding compositions having latent hardeners based on purified aldehydes of formula (I), in particular with respect to viscosity, storage stability and especially strength.

Blocking agent for amines, latent hardeners and polyurethane compositions
11518736 · 2022-12-06 · ·

The use of an aldehyde mixture containing 70 to 95 wt % of aldehydes of formula (I) and 5 to 30 wt % of alkylbenzene compounds not corresponding to formula (I) as a blocking agent for amines results in odorless, especially economically blocked amines, which at room temperature are typically liquid and have a surprisingly low viscosity. Such blocked amines are particularly suitable as latent hardeners in isocyanate-group-containing compositions. Single-component moisture-curing polyurethane compositions formulated therewith are surprisingly stable in storage, can be used for low-emission applications without odor problems and do not trigger any problems with plasticizer migration. Surprisingly, said compositions even have advantages over corresponding compositions having latent hardeners based on purified aldehydes of formula (I), in particular with respect to viscosity, storage stability and especially strength.

MOISTURE-CURABLE POLYURETHANE COMPOSITION WITH REDUCED SURFACE TACKINESS
20220363803 · 2022-11-17 · ·

A moisture-curable composition, including: a) at least one polyurethane polymer P having isocyanate groups; b) at least one blocked polyamine BA having blocked, hydrolytically activatable amino groups; and c) at least one monoamine MA of formula (V),

##STR00001##

where R.sup.a represents a linear, cyclic, or branched alkyl or alkenyl radical or optionally substituted aryl radical with 1 to 12 C atoms and optionally including ether oxygen atoms; R.sup.b and R.sup.c either independently represent a rest R.sup.a or a hydrogen atom, where at least one of R.sup.b and R.sup.c is a hydrogen atom, or R.sup.b and R.sup.c together with the N atom of monoamine MA form an aldimine group that under influence of water hydrolyzes to a aldehyde and an amine R.sup.a—NH.sub.2; wherein polymer P is the reaction product of 2,4- and/or 2,6-toluylene diisocyanate (TDI) and at least one polyol, wherein the polyol has an average functionality of >2.

MOISTURE-CURABLE POLYURETHANE COMPOSITION WITH REDUCED SURFACE TACKINESS
20220363803 · 2022-11-17 · ·

A moisture-curable composition, including: a) at least one polyurethane polymer P having isocyanate groups; b) at least one blocked polyamine BA having blocked, hydrolytically activatable amino groups; and c) at least one monoamine MA of formula (V),

##STR00001##

where R.sup.a represents a linear, cyclic, or branched alkyl or alkenyl radical or optionally substituted aryl radical with 1 to 12 C atoms and optionally including ether oxygen atoms; R.sup.b and R.sup.c either independently represent a rest R.sup.a or a hydrogen atom, where at least one of R.sup.b and R.sup.c is a hydrogen atom, or R.sup.b and R.sup.c together with the N atom of monoamine MA form an aldimine group that under influence of water hydrolyzes to a aldehyde and an amine R.sup.a—NH.sub.2; wherein polymer P is the reaction product of 2,4- and/or 2,6-toluylene diisocyanate (TDI) and at least one polyol, wherein the polyol has an average functionality of >2.

Clearcoat compositions and methods of forming clearcoat compositions

Clearcoat compositions and methods for forming a clearcoat compositions are provided. In one example, a clearcoat composition includes a binder portion A that includes a polyaspartic ester resin. An activator portion B includes a polyol-modified isocyanate that is a reaction product of a polyisocyanate component and a polyol component. The polyol component includes polycaprolactone polyol.

Flame-retardant adhesive and sealant with improved mechanical properties

A moisture-curable composition having flame retardant properties and to the use thereof as an adhesive, sealant or coating. The composition according to the invention contains at least one moisture-reactive polymer in a proportion of 10% to 50% by weight, at least one precipitated, surface-coated aluminum trihydrate in a proportion of 30% to 60% by weight and in preferred embodiments up to 25% by weight of at least one phosphorus-containing compound and up to 20% by weight of at least one carbon additive. The inventive moisture-curable composition has excellent flame retardant properties and after curing remains resistant for a long time at high heat levels.

Flame-retardant adhesive and sealant with improved mechanical properties

A moisture-curable composition having flame retardant properties and to the use thereof as an adhesive, sealant or coating. The composition according to the invention contains at least one moisture-reactive polymer in a proportion of 10% to 50% by weight, at least one precipitated, surface-coated aluminum trihydrate in a proportion of 30% to 60% by weight and in preferred embodiments up to 25% by weight of at least one phosphorus-containing compound and up to 20% by weight of at least one carbon additive. The inventive moisture-curable composition has excellent flame retardant properties and after curing remains resistant for a long time at high heat levels.

THIXOTROPIC AGENT FOR CURABLE COMPOSITIONS

A thixotropic agent for increasing the yield point of a curable composition, wherein the thixotropic agent includes (i) at least one urea compound from the reaction of at least one isocyanate with at least one amine and (ii) at least one polyether having blocked hydroxyl groups. The thixotropic agent is preparable in a simple manner and forms a spreadable paste which is firm at room temperature. It is particularly suitable as a constituent of moisture-curing polyurethane or SMP compositions, giving a good increase in the yield point thereof, without adversely affecting storage stability or migration characteristics. It enables phthalate-free adhesives, sealants or coatings that have surprisingly good conveyability coupled with a high yield point, and do not cause any problems with odor or fogging.