Methods for forming latexes are provided. In an embodiment, such a method comprises adding a monomer emulsion comprising water, a monomer, an acidic monomer, a hydrophilic monomer, a difunctional monomer, a first reactive surfactant, and a chain transfer agent, to a reactive surfactant solution comprising water, a second reactive surfactant, and an initiator, at a feed rate over a period of time so that monomers of the monomer emulsion undergo polymerization reactions to form resin particles in a latex. The reactive surfactant solution does not comprise monomers other than the second reactive surfactant, the reactive surfactant solution does not comprise a resin seed, and the monomer emulsion does not comprise the resin seed. The latex is characterized by a viscosity in a range of from about 10 cP to about 100 cP as measured at a solid content of about 30% and at room temperature. The latexes are also provided.

Methods for forming latexes are provided. In an embodiment, such a method comprises adding a monomer emulsion comprising water, a monomer, an acidic monomer, a hydrophilic monomer, a difunctional monomer, a first reactive surfactant, and a chain transfer agent, to a reactive surfactant solution comprising water, a second reactive surfactant, and an initiator, at a feed rate over a period of time so that monomers of the monomer emulsion undergo polymerization reactions to form resin particles in a latex. The reactive surfactant solution does not comprise monomers other than the second reactive surfactant, the reactive surfactant solution does not comprise a resin seed, and the monomer emulsion does not comprise the resin seed. The latex is characterized by a viscosity in a range of from about 10 cP to about 100 cP as measured at a solid content of about 30% and at room temperature. The latexes are also provided.

An example composition is disclosed. For example, the composition includes a ultra-violet (UV) curable mixture of water, an acid, a phosphine oxide with one or more photoinitiators, a water miscible polymer, a salt, and a neutralizing agent. The composition can be used to form an electrolyte layer that can be cured in the presence of air when printing the thin-film battery.

An example composition is disclosed. For example, the composition includes a ultra-violet (UV) curable mixture of water, an acid, a phosphine oxide with one or more photoinitiators, a water miscible polymer, a salt, and a neutralizing agent. The composition can be used to form an electrolyte layer that can be cured in the presence of air when printing the thin-film battery.

Fabric care compositions that include a graft copolymer, which may include (a) a polyalkylene oxide, such as polyethylene oxide (PEG); (b) N-vinylpyrrolidone (VP); and (c) a vinyl ester, such as vinyl acetate. Methods and uses relating to such compositions and/or graft copolymers.

The present invention refers to a method for the preparation of a polymer polyol which comprises: (i) preparing an intermediate in a first reactor by polymerizing a mixture comprising: (a) a base polyol in an amount from 60 to 100 wt % of the total amount of base polyol, (b) at least one ethylenically unsaturated monomer, (c) an acylperoxide radical initiator in an amount from 50 to 90 wt % of the total amount of acylperoxide radical initiator, and (d) a preformed stabilizer in an amount from 70 to 100 wt % of the total amount of preformed stabilizer or a macromer in an amount of from 70 to 100 wt % of the total amount of macromer; (ii) polymerizing in a second reactor a mixture comprising the intermediate prepared in step (i), the balance acylperoxide radical initiator proportion, the balance preformed stabilizer or macromer proportion and the balance base polyol proportion;
wherein the at least one ethylenically unsaturated monomer is added only to the first reactor.

The present invention refers to a method for the preparation of a polymer polyol which comprises: (i) preparing an intermediate in a first reactor by polymerizing a mixture comprising: (a) a base polyol in an amount from 60 to 100 wt % of the total amount of base polyol, (b) at least one ethylenically unsaturated monomer, (c) an acylperoxide radical initiator in an amount from 50 to 90 wt % of the total amount of acylperoxide radical initiator, and (d) a preformed stabilizer in an amount from 70 to 100 wt % of the total amount of preformed stabilizer or a macromer in an amount of from 70 to 100 wt % of the total amount of macromer; (ii) polymerizing in a second reactor a mixture comprising the intermediate prepared in step (i), the balance acylperoxide radical initiator proportion, the balance preformed stabilizer or macromer proportion and the balance base polyol proportion;
wherein the at least one ethylenically unsaturated monomer is added only to the first reactor.

Disclosed herein is an aqueous latex composition comprising a substantially acrylic core-shell latex, wherein a water-retaining monomer is copolymerized to the shell. The Tg of the core ranges from about 0° C. to about 12° C., and the Tg of the shell ranges from about 13° C. to about 40° C. The mean volume average particle size of the latex ranges from about 125 nm to about 200 nm. The core-shell latex comprises at least one acrylic monomer having a solubility that ranges about 10 g/L to about 30 g/L at 30° C., and this at least one acrylic monomer is present in the shell polymer in an amount greater than about 50 wt. % of all monomers in the shell. Preferably, the at least one acrylic monomer is methyl methacrylate.

Disclosed herein is an aqueous latex composition comprising a substantially acrylic core-shell latex, wherein a water-retaining monomer is copolymerized to the shell. The Tg of the core ranges from about 0° C. to about 12° C., and the Tg of the shell ranges from about 13° C. to about 40° C. The mean volume average particle size of the latex ranges from about 125 nm to about 200 nm. The core-shell latex comprises at least one acrylic monomer having a solubility that ranges about 10 g/L to about 30 g/L at 30° C., and this at least one acrylic monomer is present in the shell polymer in an amount greater than about 50 wt. % of all monomers in the shell. Preferably, the at least one acrylic monomer is methyl methacrylate.

This invention relates to improved flexible foams prepared from polymer polyols and to a process for preparing these improved flexible foams.