Disclosed is method for on-site glyoxylation of polyacrylamide in a paper or board mill, where a discontinuous batch glyoxylation reaction of aqueous reaction mixture is performed in reactor vessel having driven agitator to form aqueous polymer composition comprising glyoxylated polyacrylamide. The method comprises forming or obtaining the aqueous reaction mixture comprising polyacrylamide base polymer and glyoxal, determining alkali consumption of the mixture, and adding to the mixture, based on determined alkali consumption, pre-determined amount of alkali for adjusting pH to 8-10. The temperature is optionally adjusted to 15-40° C. and the on-site glyoxylation reaction of polyacrylamide base polymer is allowed to proceed. Viscosity of the mixture and/or a variable related to the viscosity is measured, acid is added to the mixture for lowering pH to <8, when a predetermined end viscosity value is attained, and the aqueous polymer composition comprising glyoxylated polyacrylamide is removed from the reaction vessel.

Disclosed is method for on-site glyoxylation of polyacrylamide in a paper or board mill, where a discontinuous batch glyoxylation reaction of aqueous reaction mixture is performed in reactor vessel having driven agitator to form aqueous polymer composition comprising glyoxylated polyacrylamide. The method comprises forming or obtaining the aqueous reaction mixture comprising polyacrylamide base polymer and glyoxal, determining alkali consumption of the mixture, and adding to the mixture, based on determined alkali consumption, pre-determined amount of alkali for adjusting pH to 8-10. The temperature is optionally adjusted to 15-40° C. and the on-site glyoxylation reaction of polyacrylamide base polymer is allowed to proceed. Viscosity of the mixture and/or a variable related to the viscosity is measured, acid is added to the mixture for lowering pH to <8, when a predetermined end viscosity value is attained, and the aqueous polymer composition comprising glyoxylated polyacrylamide is removed from the reaction vessel.

Disclosed herein are graft polymers having a copolymer backbone and polycyclic aromatic hydrocarbon branches for use as a nanofiller dispersant and methods for making the same. Also disclosed are elastomeric nanocomposite compositions comprising a halobutyl rubber matrix, nanoparticles of graphite or grapheme, and the graft polymer. Such elastomeric nanocomposite compositions are suitable as tire innerliners or innertubes.

Disclosed herein are graft polymers having a copolymer backbone and polycyclic aromatic hydrocarbon branches for use as a nanofiller dispersant and methods for making the same. Also disclosed are elastomeric nanocomposite compositions comprising a halobutyl rubber matrix, nanoparticles of graphite or grapheme, and the graft polymer. Such elastomeric nanocomposite compositions are suitable as tire innerliners or innertubes.

A star block copolymer and a thermoplastic elastomer including plurality of the star block copolymers and a method of making both is taught. The star block copolymers of the present invention include a core component having a styrene oligomer wherein arms emanate from the core component and the arms are poly(isobutylene-block-styrene) diblock copolymers.

A star block copolymer and a thermoplastic elastomer including plurality of the star block copolymers and a method of making both is taught. The star block copolymers of the present invention include a core component having a styrene oligomer wherein arms emanate from the core component and the arms are poly(isobutylene-block-styrene) diblock copolymers.

Polar silane linkers are provided that attach to resins to form silane-functionalized resins. The functionalized resins can be bound to hydroxyl groups on the surface of silica particles to improve the dispersibility of the silica particles in rubber mixtures. Further disclosed are synthetic routes to provide the silane-functionalized resins, as well as various uses and end products that benefit from the unexpected properties of the silane-functionalized resins. Silane-functionalized resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the silane-functionalized resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, and wet braking performance.

Polar silane linkers are provided that attach to resins to form silane-functionalized resins. The functionalized resins can be bound to hydroxyl groups on the surface of silica particles to improve the dispersibility of the silica particles in rubber mixtures. Further disclosed are synthetic routes to provide the silane-functionalized resins, as well as various uses and end products that benefit from the unexpected properties of the silane-functionalized resins. Silane-functionalized resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the silane-functionalized resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, and wet braking performance.

Polar silane linkers are provided that attach to resins to form silane-functionalized resins. The functionalized resins can be bound to hydroxyl groups on the surface of silica particles to improve the dispersibility of the silica particles in rubber mixtures. Further disclosed are synthetic routes to provide the silane-functionalized resins, as well as various uses and end products that benefit from the unexpected properties of the silane-functionalized resins. Silane-functionalized resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the silane-functionalized resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, and wet braking performance.

A dispersant for a lubricating oil, containing at least one compound selected from a specific nitrogen-containing compound which is obtained by using, as raw materials, (A) at least one polyolefin selected from polybutene and polyisobutene, (B) at least one maleic acid compound selected from maleic acid and maleic anhydride, and (C) polyamine; a boride of the specific nitrogen-containing compound; and an acylated product of the specific nitrogen-containing compound. The polyolefin (A) satisfies at least one of the following conditions (α) and (β). (α) a ratio (Sb/Sa) of an integrated value (Sb) of a peak present at 4.40 to 5.00 ppm in a .sup.1H-NMR spectrum to an integrated value (Sa) of a peak present at 5.01 to 5.60 ppm in the 1H-NMR spectrum is 2 or more. (β) a ratio (Sd/Sc) of an integrated value (Sd) of a peak present at 1.76 to 2.10 ppm in the .sup.1H-NMR spectrum to an integrated value (Sc) of a peak present at 1.65 to 1.75 ppm in the .sup.1H-NMR spectrum is 1 or more.