Compounds containing, in one molecule thereof, a structure represented by formula (1), a structure represented by formula (2), and a structure represented by formula (3) (all the symbols are those described in the specification).

##STR00001##

are useful as epoxy resin curing agents.

A RMA crosslinkable coating composition, a method for the preparation thereof and a resulting coating having easy to clean properties useful in applications like graffiti resistant, sanitisable coatings and in flooring, the composition comprising RMA crosslinkable component with at least 2 RMA donor groups and at least 2 RMA acceptor groups characterized by having fatty components selected from the group of fatty acids, fatty alcohols, fatty amines, fatty thiols and dimeric fatty acid in an amount represented by an Oil Content OC between 0, preferably 4 and 40 wt %, and crosslinking density XLD of at least 1.4 a glass transition Tg of at least 290 in combination providing a easy to clean value ΔE less than 20. The invention also relates to RMA crosslinkable fatty resins for use in RMA crosslinkable top coatings.

A coating composition includes: (a) 60 to 90 percent by weight of an active hydrogen-containing polyester having a number average molecular weight of at least 23,000, an acid value below 5 and a hydroxyl value below 10, (b) 0.1 to 10 percent by weight of a polyanhydride, and (c) 5 to 30 percent by weight of a curing agent reactive with the active hydrogens associated with (a) and (b), the percentages being based on weight of resin solids of the coating composition, where the reaction product of the coating composition forms a single coating without including a thermoplastic polymer. The coating composition is useful in coating food and beverage containers, particularly 2-piece cans formed by drawing and redrawing (DRD).

The invention described herein generally pertains to a composition that includes a silyl-terminated polymer having silyl groups linked to a polymer backbone via triazole. The silyl-terminated polymer is a reaction product of a functionalized polymer backbone and a functionalized silane. The polymer backbone includes a first functional group, which may be one of an azide or an alkyne. The functionalized silane includes a second functional group may also be one of an azide or an alkyne, but is also different from the first functional group. The functionalized polymer backbone is reacted with the functionalized silane in the presence of a metal catalyst.

The invention described herein generally pertains to a composition that includes a silyl-terminated polymer having silyl groups linked to a polymer backbone via triazole. The silyl-terminated polymer is a reaction product of a functionalized polymer backbone and a functionalized silane. The polymer backbone includes a first functional group, which may be one of an azide or an alkyne. The functionalized silane includes a second functional group may also be one of an azide or an alkyne, but is also different from the first functional group. The functionalized polymer backbone is reacted with the functionalized silane in the presence of a metal catalyst.

The present application relates to a Michael Addition curable composition, coating composition containing the same and coated article made therefrom. In particular, the Michael Addition curable composition comprises at least one reactive donor capable of providing two or more nucleophilic carbanions; at least one reactive acceptor comprising two or more carbon-carbon double bonds; and at least one catalyst for catalyzing a Michael Addition crosslinking reaction between the at least one reactive donor and the at least one reactive acceptor, wherein the at least one reactive donor comprises at least one branched polyester comprising at least one polyester backbone and at least one —C(O)—CH.sub.2—C(O)-moiety; wherein the at least one polyester backbone is derived from an alcohol component comprising at least one alcohol having at least three hydroxyl groups; and wherein the at least one branched polyester has a —C(O)—CH.sub.2—C(O)-moiety equivalent of no more than 700 g/mol.

A macromolecule comprises a ring-opened polymerized product of β-lactone monomers of formula I:

##STR00001## and having a structure of formula IA:

##STR00002## wherein R.sub.1 is an alkyl group having at least 8 carbon atoms. The macromolecule may be hydroxy-terminated, and may be copolymerized with other β-lactone monomers having different substituting groups and/or with higher lactone monomers. The macromolecule may be used as a reactant to form an alkoxysilane-terminated polymer, a polyurethane, or a (co)polyester, or may be used as an elastomeric midblock in a triblock copolymer having hard end blocks, such as polylactic acid. Such triblock systems demonstrate two discreet regions having properties similar to styrene block copolymers and are therefore suitable for use as hot melt or pressure-sensitive adhesives. In some embodiments, such triblock polymers may be entirely bio-sourced and compostable.

A method of preparing polyester elastomer meltblown nonwoven fabric membrane with porous and high bonding strength includes the following steps of: (a) Adding a reaction solvent to a reaction solvent to thermoplastic polyester elastomer (TPEE) powder or granules to prepare a solvent mixture. (b) Adding a modifier to the solvent mixture, and mixing uniformly to prepare a first mixture, the modifier includes at least one of o-xylylenediamine, m-xylylenediamine, alpha, alpha′-diamino-p-xylene, 2,3,5,6-Tetrachloro-p-xylene-alpha,alpha′-diamine, and 1,3,5,7-Tetraazatricyclodecane. (c) Adding an initiator to the first mixture, and mixing uniformly to prepare a second mixture. (d) Drying the second mixture to form a masterbatch, and (e) preparing the polyester elastomer meltblown nonwoven fabric membrane by passing the masterbatch through a meltblown process.

A process of preparing a compounded hydrostable poly(aliphatic ester-carbonate) comprises providing a hydrostable poly(aliphatic ester-carbonate), compounding in an extruder the hydrostable poly(aliphatic ester-carbonate) and 0.05 wt % to 0.60 wt % of a multifunctional epoxide compounding stabilizer, based on the total weight of the compounded hydrostable poly(aliphatic ester-carbonate), under vacuum of 17000 to 85000 Pascals, and a torque of 30% to 75%, to provide the compounded hydrostable poly(aliphatic ester-carbonate). After compounding, at least one of the following apply: the inter-sample variability in molecular weight is less than 5%, wherein inter-sample variability is determined by comparing five 100 mil chips of the compounded hydrostable poly(aliphatic ester-carbonate); the % weight average molecular weight (MW) difference is less than 5% after hydroaging at 85° C. and 85% humidity; or the compounded poly(aliphatic ester-carbonate) has less than 75 ppm of unreacted —COOH end groups measured by .sup.31P NMR.

The invention provides a method for the production of a cross-linked polyester moulded article.