There is described an acrylic polyester resin, obtainable by grafting an acrylic polymer with a polyester material. The polyester material is obtainable by polymerizing (i) a polyacid component, with (ii) a polyol component, including—2,2,4,4-tetraallcylcyclobutane-1,3-diol. One of the polyacid component or the polyol component comprises a functional monomer operable to impart functionality on to the polyester resin, such that an acrylic polymer may be grafted with the polyester material via the use of said functionality. Also provided is an aqueous coating composition comprising the acrylic polyester resin and a metal packaging containing coated with the composition.

An object of the present invention is to provide an antistatic agent which imparts excellent antistatic properties to thermoplastic resins. The antistatic agent (Z) of the present invention contains a block polymer (A) having a block of a polyamide (a) and a block of a polyether (b1) as structure units, wherein the polyether (b1) contains propylene oxide (PO) and ethylene oxide (EO) as constituent monomers, and a weight ratio of the propylene oxide (PO) to the ethylene oxide (EO), i.e., propylene oxide (PO)/ethylene oxide (EO), is 1/99 to 25/75.

An object of the present invention is to provide an antistatic agent which imparts excellent antistatic properties to thermoplastic resins. The antistatic agent (Z) of the present invention contains a block polymer (A) having a block of a polyamide (a) and a block of a polyether (b1) as structure units, wherein the polyether (b1) contains propylene oxide (PO) and ethylene oxide (EO) as constituent monomers, and a weight ratio of the propylene oxide (PO) to the ethylene oxide (EO), i.e., propylene oxide (PO)/ethylene oxide (EO), is 1/99 to 25/75.

A biodegradable polyester is provided. The biodegradable polyester is a transesterification or esterification reaction product of a reactant (a) and a reactant (b). The reactant (a) is a modified linear saccharide oligomer. The reactant (b) is a polyester, or the reactant (b) includes a dicarboxylic acid and a diol. The modified saccharide oligomer is a reaction product of a saccharide oligomer and a modifier.

A resin composition comprising a polycarbonate-polyorganosiloxane copolymer (A) comprising a polycarbonate block (A-1) comprising a repeating unit represented by the following general formula (I) and a polyorganosiloxane block (A-2) comprising a repeating unit represented by the following general formula (II); and carbon fibers (B), the carbon fibers (B) being carbon fibers to which a compound having an epoxy group is attached:

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There is described an aqueous coating composition, the aqueous coating composition comprising an acrylic polyester resin, obtainable by grafting an acrylic polymer and a polyester material, the polyester material being obtainable by polymerizing: (i) a polyacid component, with (ii) a polyol component. At least one of the polyacid component and/or the polyol component comprises a functional monomer operable to impart functionality on to the polyester resin, such that an acrylic polymer may be grafted with the polyester material via the use of said functionality. The coating composition further containing a crosslinking material, wherein the crosslinking material comprises material according to formula (I); as shown in claim 1; wherein R.sub.1 is selected from aryl (such as C.sub.4 to C.sub.24 aryl), or aralkyl (such as C.sub.5 to C.sub.25 aralkyl); R.sub.2 to R.sub.5 are each independently hydrogen, alkyl (such as C.sub.1 to C.sub.20 alkyl), aryl (such as C.sub.4 to C.sub.24 aryl), aralkyl (such as C.sub.5 to C.sub.25 aralkyl) or —CHR.sub.8OR.sub.9; wherein R.sub.8 and R.sub.9 are each independently hydrogen, alkyl (such as C.sub.1 to C.sub.20 alkyl), aryl (such as C.sub.4 to C.sub.24 aryl), aralkyl (such as C.sub.5 to C.sub.25 aralkyl), alkoxyalkyl (such as C.sub.2 to C.sub.40 alkoxyalkyl) or an alkaryl (such as C.sub.5 to C.sub.25 alkaryl); wherein at least one of R.sub.2 to R.sub.5, is —CHR.sub.8OR.sub.9, suitably all of R.sub.2 to R.sub.5, are —CHR.sub.8OR.sub.9.

A cross-linkable hydrogel composition comprising an aqueous base carrier composition and a cross-linkable hydrogel precursor, wherein the aqueous base carrier composition comprises one or more polymers and one or more nanoparticles, wherein the one or more polymers are selectively adsorbed to the one or more nanoparticles, and wherein the one or more polymers and the one or more nanoparticles form a shear-thinning and self-healing hydrogel and wherein the one or more polymers and the one or more nanoparticles and cross-linkable hydrogel precursor are each comprised in the cross-linkable hydrogel composition in a concentration at which neither the one or more polymers nor the nanoparticles, taken alone, form a hydrogel, characterized in that the cross-linkable hydrogel precursor is not selectively adsorbed to the one or more nanoparticles and in that the cross-linkable hydrogel precursor and the one or more nanoparticles don't form a transient shear-thinning and self-healing hydrogel.

A drilling fluid includes an aqueous phase, a clay-based component, and an amphiphilic branched star polymer. The amphiphilic branched star polymer is a crosslinked, polymerized reaction product of crosslinker C, hydrophobic monomer B, and hydrophilic monomer A. The crosslinked polymerized reaction product includes a plurality of block copolymer segments of hydrophobic monomer B and hydrophilic monomer A interconnected via crosslinker C.

Disclosed is a preparation method for polylactic acid grafted chitosan nanowhiskers, and belongs to the technical field of materials. The preparation method of the disclosure is that after lactide, a catalyst and chitosan are uniformly mixed, polymerization grafting is performed to prepare PLA-g-CS, and then the PLA-g-CS is dispersed into an alkali liquor to obtain nanowhiskers by a repeated freezing/unfreezing method, with no solvent used in a polymerization grafting process. The method has advantages that the nanowhiskers can be prepared from the PLA-g-CS without a good solvent, and the whole reaction is efficient, clean, and environmentally friendly.

Disclosed is a preparation method for polylactic acid grafted chitosan nanowhiskers, and belongs to the technical field of materials. The preparation method of the disclosure is that after lactide, a catalyst and chitosan are uniformly mixed, polymerization grafting is performed to prepare PLA-g-CS, and then the PLA-g-CS is dispersed into an alkali liquor to obtain nanowhiskers by a repeated freezing/unfreezing method, with no solvent used in a polymerization grafting process. The method has advantages that the nanowhiskers can be prepared from the PLA-g-CS without a good solvent, and the whole reaction is efficient, clean, and environmentally friendly.