Vapor phase polymerization can be used to synthesize a 3D porous network of polystyrene-containing, branched carbon nanofibers on polyurethane(s), optionally using natural light (NL) initiation. NL styrene polymerization in a confined reactor containing CNF-grafted PU can provide a stable porous network. The NL can vaporize the styrene by increasing the reactor temperature and generate styrene radicals. Without CNF, the polymerization on polyurethane (PU) provides a delicate, fragile surface. Radical styrene in vapor phase can interact with CNF to produce polystyrene branches by generating active sites on CNF, while reinforcing the 3D porous structure. After polymerization, the PU surface area increased from 9 to 184 m.sup.2/g and pore size decreased from 2567 to 10 . 3D porous networks of NL-assisted PS branched CNF supported PU can provide a hydrophobic, oleophilic surface with a water contact angle of approx 1483, rapidly gravity separating hexane and water without external force.

Provided is a rubber-containing graft polymer which is excellent in mechanical strength such as weld strength or impact strength, required as a rubber-containing graft polymer. A rubber-containing graft polymer (A) of the present invention is a rubber-containing graft polymer having a graft chain, in which when the rubber-containing graft polymer is mixed with an organic solvent and separated into an organic solvent insoluble component and an organic solvent soluble component, a caprolactone unit is contained in a graft chain contained in the organic solvent insoluble component.

Provided is a rubber-containing graft polymer which is excellent in mechanical strength such as weld strength or impact strength, required as a rubber-containing graft polymer. A rubber-containing graft polymer (A) of the present invention is a rubber-containing graft polymer having a graft chain, in which when the rubber-containing graft polymer is mixed with an organic solvent and separated into an organic solvent insoluble component and an organic solvent soluble component, a caprolactone unit is contained in a graft chain contained in the organic solvent insoluble component.

The invention relates to an aqueous dispersion for use as open time improver in a coating composition which aqueous polymer dispersion comprises a first polymer having a number average molecular weight (Mn) of from 2,000 to 120,000 (determined by gel permeation chromatography using a mixture of tetrahydrofurane and acetic acid as eluent), an acid value of from 30 to 150 mg KOH/g, and an ethylene-oxide wt % (on total solid polymer) of from 1 to 20 wt %, said first polymer dispersion being obtainable by free radical polymerization of a monomer mixture in the presence of at least one free-radical initiator and at least one surfactant, said monomer mixture comprising: a) 5 to 20 wt %, preferably 7 to 10 wt %, acid functional ethylenically unsaturated monomers or precursors thereof or ethylenically unsaturated monomers comprising ionic group precursors; b) 5 to 25 wt %, preferably 7 to 20 wt %, ethylenically unsaturated monomers containing polyethylene oxide, polyethylene glycol or mono-alkoxypolyethylene glycol moeity c) up to 90 wt % of non-ionic ethylenically unsaturated monomers other than a) or b); d) 0 to 10 wt % ethylenically unsaturated monomers with a functional group for cross-linking e) 0 to 10 wt % of chain transfer agents; f) up to 90 wt % non-ionic ethylenically unsaturated monomers other than c), wherein 30 to 90 wt %, more preferably 60 to 80 wt % comprise crosslinkable groups or precursors thereof; wherein the sum of a) through f) is 100 wt %.

The invention further relates to a method for making the first polymer dispersion, the use of said aqueous dispersion as an open time improver in a coating composition, to aqueous coating compositions comprising a blend of at least a first aqueous polymer dispersion and a second aqueous polymer dispersion comprising a film-forming second polymer and to a method for making said coating composition

The invention relates to an aqueous dispersion for use as open time improver in a coating composition which aqueous polymer dispersion comprises a first polymer having a number average molecular weight (Mn) of from 2,000 to 120,000 (determined by gel permeation chromatography using a mixture of tetrahydrofurane and acetic acid as eluent), an acid value of from 30 to 150 mg KOH/g, and an ethylene-oxide wt % (on total solid polymer) of from 1 to 20 wt %, said first polymer dispersion being obtainable by free radical polymerization of a monomer mixture in the presence of at least one free-radical initiator and at least one surfactant, said monomer mixture comprising: a) 5 to 20 wt %, preferably 7 to 10 wt %, acid functional ethylenically unsaturated monomers or precursors thereof or ethylenically unsaturated monomers comprising ionic group precursors; b) 5 to 25 wt %, preferably 7 to 20 wt %, ethylenically unsaturated monomers containing polyethylene oxide, polyethylene glycol or mono-alkoxypolyethylene glycol moeity c) up to 90 wt % of non-ionic ethylenically unsaturated monomers other than a) or b); d) 0 to 10 wt % ethylenically unsaturated monomers with a functional group for cross-linking e) 0 to 10 wt % of chain transfer agents; f) up to 90 wt % non-ionic ethylenically unsaturated monomers other than c), wherein 30 to 90 wt %, more preferably 60 to 80 wt % comprise crosslinkable groups or precursors thereof; wherein the sum of a) through f) is 100 wt %.

The invention further relates to a method for making the first polymer dispersion, the use of said aqueous dispersion as an open time improver in a coating composition, to aqueous coating compositions comprising a blend of at least a first aqueous polymer dispersion and a second aqueous polymer dispersion comprising a film-forming second polymer and to a method for making said coating composition

The invention relates to an aqueous dispersion for use as open time improver in a coating composition which aqueous polymer dispersion comprises a first polymer having a number average molecular weight (Mn) of from 2,000 to 120,000 (determined by gel permeation chromatography using a mixture of tetrahydrofurane and acetic acid as eluent), an acid value of from 30 to 150 mg KOH/g, and an ethylene-oxide wt % (on total solid polymer) of from 1 to 20 wt %, said first polymer dispersion being obtainable by free radical polymerization of a monomer mixture in the presence of at least one free-radical initiator and at least one surfactant, said monomer mixture comprising: a) 5 to 20 wt %, preferably 7 to 10 wt %, acid functional ethylenically unsaturated monomers or precursors thereof or ethylenically unsaturated monomers comprising ionic group precursors; b) 5 to 25 wt %, preferably 7 to 20 wt %, ethylenically unsaturated monomers containing polyethylene oxide, polyethylene glycol or mono-alkoxypolyethylene glycol moeity c) up to 90 wt % of non-ionic ethylenically unsaturated monomers other than a) or b); d) 0 to 10 wt % ethylenically unsaturated monomers with a functional group for cross-linking e) 0 to 10 wt % of chain transfer agents; f) up to 90 wt % non-ionic ethylenically unsaturated monomers other than c), wherein 30 to 90 wt %, more preferably 60 to 80 wt % comprise crosslinkable groups or precursors thereof; wherein the sum of a) through f) is 100 wt %. The invention further relates to a method for making the first polymer dispersion, the use of said aqueous dispersion as an open time improver in a coating composition, to aqueous coating compositions comprising a blend of at least a first aqueous polymer dispersion and a second aqueous polymer dispersion comprising a film-forming second polymer and to a method for making said coating composition.

The invention relates to an aqueous dispersion for use as open time improver in a coating composition which aqueous polymer dispersion comprises a first polymer having a number average molecular weight (Mn) of from 2,000 to 120,000 (determined by gel permeation chromatography using a mixture of tetrahydrofurane and acetic acid as eluent), an acid value of from 30 to 150 mg KOH/g, and an ethylene-oxide wt % (on total solid polymer) of from 1 to 20 wt %, said first polymer dispersion being obtainable by free radical polymerization of a monomer mixture in the presence of at least one free-radical initiator and at least one surfactant, said monomer mixture comprising: a) 5 to 20 wt %, preferably 7 to 10 wt %, acid functional ethylenically unsaturated monomers or precursors thereof or ethylenically unsaturated monomers comprising ionic group precursors; b) 5 to 25 wt %, preferably 7 to 20 wt %, ethylenically unsaturated monomers containing polyethylene oxide, polyethylene glycol or mono-alkoxypolyethylene glycol moeity c) up to 90 wt % of non-ionic ethylenically unsaturated monomers other than a) or b); d) 0 to 10 wt % ethylenically unsaturated monomers with a functional group for cross-linking e) 0 to 10 wt % of chain transfer agents; f) up to 90 wt % non-ionic ethylenically unsaturated monomers other than c), wherein 30 to 90 wt %, more preferably 60 to 80 wt % comprise crosslinkable groups or precursors thereof; wherein the sum of a) through f) is 100 wt %. The invention further relates to a method for making the first polymer dispersion, the use of said aqueous dispersion as an open time improver in a coating composition, to aqueous coating compositions comprising a blend of at least a first aqueous polymer dispersion and a second aqueous polymer dispersion comprising a film-forming second polymer and to a method for making said coating composition.

The present invention involves a 100% solids, radiation curable adhesive formulation for adhesion to EVA. This formulation may have varying compositions, as discussed in detail herein. However primarily the composition may comprise at least a monomer, and a chlorinated additive. Photo initiators may be used to allow for low temperature UV or other radiation curing. Other additives may be used to enhance functional features in various ways. In use, the present invention may be coated on a surface of EVA and then cured, and may be adhered to a substrate using only a layer of adhesive on the substrate, in contrast to the structures of the prior art, which require at least two sided adhesive application, among other complexities.

The present invention involves a 100% solids, radiation curable adhesive formulation for adhesion to EVA. This formulation may have varying compositions, as discussed in detail herein. However primarily the composition may comprise at least a monomer, and a chlorinated additive. Photo initiators may be used to allow for low temperature UV or other radiation curing. Other additives may be used to enhance functional features in various ways. In use, the present invention may be coated on a surface of EVA and then cured, and may be adhered to a substrate using only a layer of adhesive on the substrate, in contrast to the structures of the prior art, which require at least two sided adhesive application, among other complexities.

The present invention discloses a method of preparing polymeric photoluminescent dots in water using inexpensive non-conjugated polymers. The resulting polymeric photoluminescent dots display the following properties: excellent water dispersibility, low toxicity, high absorptivity, good photo-stability and high quantum yield. The photoluminescent properties are not influenced by aggregation-caused quenching effect. The method is amenable to scale-up and is environmentally friendly.