Abstract: This invention relates to hydrolysis resistant, water-soluble ammonium salt solids which are biologically active and which are described by the formula ##STR1## wherein m has a value of from 1 to 3; n has a value of from 1 to 4 and is equal to the free valences in anion R; p has a value of from 1 to 3; R.sub.1, R.sub.2 and R.sub.3 are each independently selected from the group of hydrogen, and C.sub.1 to C.sub.2 alkyl; R.sub.5 and R.sub.6 are each independently selected from the group of hydrogen, hydroxyalkyl and alkoxyalkyl radicals having from 1 to 10 carbon atoms and R is the anion of a biologically active, water-insoluble anion having at least 1 deprotonized hydrogen and is derived from a biologically active, acidic, organic compound selected from the group of a carboxylic, thiocarbonic, sulfonic, sulfinic, thiosulfonic, thioacid, mono- and di-thiophosphate and phosphorous containing acid, having a pKa* value less than 5.

Abstract: Crosslinkable copolymers of (a) 80-99% by wt. vinylpyrrolidone (VP) and 1-20% by wt. of a tertiary-amine-containing polymerizable monomer, e.g. vinylimidazole (VI) or 4-vinylpyridine (VPy), and (b) 80-99% by wt. VP and 1-20% by wt. of an epoxide-containing polymerizable monomer, e.g. allyl glycidyl ether (AGE) or glycidyl acrylate (GA), are reacted in solution, e.g. water, alcohol, or mixtures thereof, at a predetermined temperature, e.g. 50.degree.-70.degree. C., in a wt. ratio (solids basis) of (a):(b) of about 2:1 to 1:2, preferably about 1:1, in a solution concentration of about 10-30% of each, to provide a crosslinked PVP product, in gel form, suitable for use as an electrolead on a conductive foilbacking, or for bandages and wound dressings, and as a controlled release media for pharmaceuticals.

Abstract: A process for making a solution of PVP K-90 polymer having a weight average molecular weight, Mw, of about 630,000 to 750,000 and a molecular weight distribution, Mw/Mn, where Mn is the number average molecular weight of the polymer, of 5 or less, which comprises free radical polymerizing about 5-30% by weight vinylpyrrolidone, preferably 10-20%, at about 40.degree.-100.degree. C., preferably 60.degree.-75.degree. C., in an aqueous-alcohol solvent selected from the group consisting of about (a) 5% isopropanol-95% water, (b) 10% ethanol-90% water and (c) 20% methanol-80% water.

Abstract: The invention relates to properties and uses of N-hydrocarbon substituted lactams, particularly N-alkyl substituted lactams having the formula ##STR1## wherein R' is a hydrophobic radical such as linear or branched chain alkyl group containing from 8 to 27 carbon atoms, most preferably micelle forming pyrrolidones having 12 to 16 carbon atoms in the R' group. The invention particularly relates to the uses of the N-hydrocarbon substituted lactams which involve surfactant properties, such as solubility, wetting, viscosity building, emulsifying and/or complexing properties.

Abstract: Crosslinkable copolymers of (a) 80-99% by wt. vinylpyrrolidone (VP) and 1-20% by wt. of a tertiary-amine-containing polymerizable monomer, e.g. vinylimidazole (VI) or 4-vinylpyridine (VPy), and (b) 80-99% by wt. VP and 1-20% by wt. of an epoxide-containing polymerizable monomer, e.g. allyl glycidyl ether (AGE) or glycidyl acrylate (GA), are reacted in solution, e.g. water, alcohol, or mixtures thereof, at a predetermined temperature, e.g. 50.degree.-70.degree. C., in a wt. ratio (solids basis) of (a):(b) of about 2:1 to 1:2, preferably about 1:1, in a solution concentration of about 10-30% of each, to provide a crosslinked PVP product, in gel form, suitable for use as an electrolead on a conductive foilbacking, or for bandages and wound dressings, and as a controlled release media for pharmaceuticals.

Abstract: A pharmaceutical tablet is provided herein having an effective dissolution rate. The tablet contains a pharmaceutically-active ingredient and a substantially linear, i.e. non-crosslinked K-30 to K-120 PVP as a binding agent. The PVP used herein is made by an initiated polymerization process in which vinyl pyrrolidone monomer is polymerized in the presence of an initiator which produces a linear PVP polymerization, i.e. is a poor hydrogen abstractor of PVP polymer backbones, which would produce a disadvantageous crosslinked PVP product. Suitable initiators include low energy peroxyester free radical initiators, such as t-amylperoxy pivalate, an azo initiator, or a redox initiator which can perform at low temperatures.Preferably the residual initiator level in the PVP is reduced to less than 500 ppm, thereby further precluding the possibility of crosslinking of the PVP polymer during the shelf-life of the tablet.

Abstract: What is provided herein are conditioning hair care compositions comprising (a) a stabilized silicone product obtained by in situ polymerization of a water-soluble vinyl monomer, preferably vinylpyrrolidone, in the presence of discrete microdroplets of a silicone oil in water, (b) an emulsifiers, (c) a thickener, optionally, (d) a cationic surfactant, and the balance being (e) water.

Abstract: What is provided herein are conditioning shampoo hair care compositions comprising (a) a stabilized silicone product obtained by in situ polymerization of a water-soluble vinyl monomer, preferably vinylpyrrolidone, in the presence of discrete microdroplets of a silicone oil in water, (b) a surfactant, (c) a foam stabilizer, and the balance being (d) water.

Abstract: Vinylpyrrolidone and vinylcaprolactam residual monomers are removed from their respective crosslinked and non-crosslinked, vinyl lactam homopolymers, vinyl lactam copolymers and vinyl lactam terpolymers containing substantially contaminating amounts of residual vinylpyrrolidone or vinylcaprolactam monomer by a process which comprises (1) adjusting the pH of the vinyl lactam polymer slurry containing from about 1 to about 30 wt. % solids or a solution of the vinyl lactam polymer to a pH of less than 5 with an acid selected from the group of sulfuric, phosphoric, carbonic, formic and acetic acids and mixtures thereof; (2) reacting the acid with the residual vinyl lactam monomer at a temperature of from about 50.degree. to about 150.degree. C. for a period of from about 0.5 to about 10 hours until the residual monomer is reduced to less than 5 ppm and (3) drying said solids to a substantially pure vinyl lactam polymeric product in a free-flowing particulate state.

Abstract: A method of crosslinking polyvinylpyrrolidone (PVP) at a predetermined pH which comprises (a) providing a tertiary amino-functional PVP as a starting material, (b) condensing said starting material with a predetermined amount of epichlorohydrin to form an epichlorohydrin-functional PVP copolymer, and, if less than an equivalent of epichlorohydrin in use, unreacted starting material, (c) acidifying the resultant copolymer to form a solution of a storage stable glycidyl quat intermediate, and (d) increasing the pH of the solution to above 7 to convert the glycidyl quat into a glycidyl epoxide, and (e) crosslinking the glycidyl epoxide with free amine group on the copolymer or as added amine functional PVP copolymer to form a crosslinked PVP polymer.

Abstract: A charge imbalanced polymer is made by:reacting 1 mole of an anhydride compound having the formula ##STR1## where R is C.sub.1 -C.sub.4 alkyl, with less than 1 mole of a mixture of about 0.1-0.8 mole of a compound having the formula ##STR2## where n is 1-6, R.sub.1 and R.sub.2 are independently C.sub.1 -C.sub.6 alkyl, and R.sub.3 is H or lower alkyl, and about 0.50-0.4 mole of a compound having the formula ##STR3## where R.sub.4 is C.sub.12 -C.sub.24 alkyl, and where (A) is 2-6 times (B), isolating the product, andhydrolyzing any residual anhydride compound in water to the corresponding diacid compound.

Abstract: A hair spray composition is provided herein which is capable of delivering a fine finishing mist at a high resin solids level. The composition is substantially moisture resistant, provides a stiff resin film having excellent hair holding power, and has a relatively low concentration of volatile organic compounds therein. The composition of the invention attains its unique attributes by including therein a water soluble or dispersible alkylated polyvinylpyrrolidone (PVP) copolymer powders having a predetermined blend of two monomer components, one being PVP having a defined molecular weight (K-value 15-120, preferably 30-90) and concentration (80-99%, preferably 90-95%) and the other being an alkylene having a selected number of carbon atoms (C.sub.4 -C.sub.10, preferably (C.sub.6 -C.sub.8), linear or branched, in a defined concentration (1-20%, preferably 5-10%).

Abstract: This invention relates to hydrolysis resistant, water-soluble ammonium salt solids which are biologically active and which are described by the formula ##STR1## wherein m has a value of from 1 to 3; n has a value of from 1 to 4 and is equal to the free valences in anion R; p has a value of from 1 to 3; R.sub.1, R.sub.2 and R.sub.3 are each independently selected from the group of hydrogen, and C.sub.1 to C.sub.2 alkyl; R.sub.5 and R.sub.6 are each independently selected from the group of hydrogen, hydroxyalkyl and alkoxyalkyl radicals having from 1 to 10 carbon atoms and R is the anion of a biologically active, water-insoluble anion having at least 1 deprotonized hydrogen and is derived from a biologically active, acidic, organic compound selected from the group of a carboxylic, thiocarbonic, sulfonic, sulfinic, thiosulfonic, thioacid, mono- and di- thiophosphate and phosphorous containing acid, having a pKa* value less than 5.

Abstract: The method of crosslinking polyvinylpyrrolidone (PVP) which comprises: copolymerizing vinyl pyrrolidone (VP) and an aminoalkene, a hydroxyalkene, or an aminoalkyl acrylamide or methacrylamide, to provide a crosslinkable, functional PVP copolymer as a starting material; then (a) condensing predetermined amounts of the starting material and a haloacetal under basic conditions to form a stable, crosslinkable PVP copolymer intermediate containing an acetal group as a functional appendant on the PVP polymer backbone; (b) acidifying the basic solution to hydrolyze the acetal group to an aldehyde group, and (c) crosslinking the aldehyde-functional PVP copolymer with the amine group of the amine-functional PVP copolymer, present on the polymer as free amine after step (a), or as added amine-functional copolymer to the reaction mixture, under basic conditions.

Abstract: What is provided herein is a stabilized aqueous solution of a C.sub.1 -C.sub.5 alkyl vinyl ether and maleic acid copolymer which includes about 10-500 ppm of an inorganic reducing agent as a stabilizing additive, said reducing agent being effective to prevent oxygen from the air and peroxides contained in polymer system from degrading the copolymer. Preferably the reducing agent is sulfur dioxide and salts derived from sulfur dioxide and alkali metals such as, sodium or potassium bisulfite, sodium or potassium metabisulfite, sodium or potassium thiosulfite, or sodium or potassium sulfite.

Abstract: A charge imbalanced composition comprising:(a) about 10 to 90 mole % of an amphoteric copolymer having the formula ##STR1## where R=alkyl C.sub.1 -C.sub.4,N=1-6,R.sub.1 and R.sub.2 are independently alkyl C.sub.1 -C.sub.6, andR.sub.3 is H,(b) about 10 to 90 mole % of a polymeric diacid having the formula: ##STR2## where R is as defined above, and(c) less than about 8 mole % of by-product salts which are the dialkylaminoalkylamine salts of (a) and (b).The composition described above is made by:reacting 1 mole of an anhydride compound having the formula ##STR3##where R is as defined above,with less than 1 mole of a compound having the formula ##STR4## where n, R.sub.1 and R.sub.2 are as defined above, and R.sub.3 is H, isolating the product, andhydrolyzing any residual anhydride compound in water to the corresponding diacid compound.

Abstract: Crosslinkable, functional polymers of vinylpyrrolidone and aminoalkyl acrylamides are provided herein. Such polymers are readily crosslinked with a crosslinking agent, e.g. a multi-aldehyde, such as a di-, tri- or tetra- aldehyde, preferably, glutaric dialdehyde, to form an aqueous gel of predetermined viscosity suitable for making hydrogels, adhesives and coatings.

Abstract: Urea-hydrogen peroxide-polyvinylpyrrolidone (PVP) in the form of a free-flowing powder is stable against decomposition in water and alcohol solvents. The product is obtained by spraying an aqueous solution of urea-hydrogen peroxide onto a fluidized bed of PVP and drying; it contains about 5%-20% by weight H.sub.2 O.sub.2 and less than about 5% water. The urea-hydrogen peroxide solution is applied onto the fluidized PVP bed at a predetermined rate, suitably about 0.5-30 g of solution/minute/kg PVP in the bed, and, preferably, about 1-3 g/min/kg PVP.

Abstract: What is provided herein are copolymers of a vinyl lactam and a hydroxy or amino alkene monomers, which contain a hydroxy or amino functionality therein. These copolymers are prepared by reaction between a vinyl lactam, e.g. vinylpyrrolidone (VP) or vinyl caprolactam (VCL), a functional polymerizable monomer, e.g. .omega.-amino-1-alkene (AA) or .omega.-hydroxy-1-alkene (HA), in water solution in the presence of a free radical initiator under predetermined reaction conditions.

Abstract: Copolymers of vinyl pyrrolidone and a quaternary ammonium monomer complexed with H.sub.2 O.sub.2 in the form of free-flowing powders is described. The products are made in a fluidized bed of said copolymer maintained at a reaction temperature of from room temperature to about 60.degree. C. The fluidized bed is contacted with finely divided droplets of a 30 to 85% by weight aqueous H.sub.2 O.sub.2 solution at a feed rate of about 1-10 g/minute/kg copolymer present. The copolymer-H.sub.2 O.sub.2 product preferably contains about 10-20% H.sub.2 O.sub.2 (1:1 molar ratio), and less than about 5% water. The product can be used as a hair bleach enhancer which provides dual hair conditioning properties.