Abstract: Improved non-crosslinked and non-degraded amphoteric starch derivatives containing tertiary amino or quaternary ammonium groups and anionic phosphate groups are disclosed. The derivatives which are defined by a minimum bound phosphorus content, a minimum viscosity and other criteria have use as wet-end additives and provide improved drainage properties in the manufacture of paper.

Abstract: High solids, low viscosity, alkaline-curable, thermosetting cationic vinyl ester based polymer latices, characterized by the high molecular weight of the polymer therein, are prepared by polymerizing at least 5% of selected vinyl esters (up to C.sub.6), 0.5-10% of a self-crosslinking cationic quaternary ammonium monomer, and optionally a vinyl polymerizable monomer such as butyl acrylate, ethylene, acrylamide, diallyl maleate, and/or 2-hydroxyethyl acrylate. The polymerization is carried out in the presence of water, a watersoluble cationic azo initiator, a water-soluble amino thiol salt chain transfer agent, and a cationic and/or nonionic surfactant. The latices are useful as formaldehyde-free binders for polyester nonwovens.

Abstract: Conventional carboxylated neoprene latex adhesives are improved with respect to their metal adhesion, heat and water resistance and bonding range by the addition thereto of an epoxy resin, preferably an epoxy resin prepared by the reaction of para-aminophenol with epichlorohydrin.

Abstract: This invention provides cementiferous compositions having improved flow characterisitics which are given by the incorporation of certain hydroxy acrylate copolymers. Typical copolymers are of acrylic or methacrylic acid with a hydroxyalkyl acrylate or methacrylate and are used preferably in the range 0.01% to 2.5% w/w on the cement in the cementiferous composition. This invention also provides novel additive compositions for use in the cementiferous compositions.

Abstract: Graft copolymers of cellulose derivatives and N,N-diallyl,N-N-dialkyl ammonium chlorides or bromides are prepared using a dry or substantially solvent-free system by impregnating a concentrated aqueous solution of the N,N-diallyl-N,N-dialkyl ammonium halide, water soluble surfactant and catalyst onto the dry cellulose substrate, heating the reaction mass for sufficient time to achieve polymerization and then drying.

Abstract: The metal adhesion and heat and water resistance of conventional neoprene latex adhesives are improved by the addition thereto of a polyfunctional amine and an epoxy resin wherein for every 100 parts by weight of dry neoprene, the epoxy is added in an amount of 10-40 parts and the amine is added in an amount sufficient to provide 50-150% of the stoichiometric amount required to cure the epoxy.

Abstract: Hot melt adhesive compositions are prepared from ethylene copolymers, atactic polypropylene, tackifying resins and optional additives. The adhesives are non-pressure sensitive and are characterized by high cohesive strength, strong tack, and good heat, creep and cold resistance. In accordance with the preferred embodiment, the adhesives are formulated so as to be particularly adaptable for use in the construction of disposable diapers of the multi-line construction variety.

Abstract: Quaternary ammonium monomers and monomers copoylmerizable therewith are reacted in the presence of anionic polymers to directly form a dry coacervate by a process which comprises forming a solution comprising the monomer(s), the anionic polymer, solvent(s) and a free-radical initiator and simultaneously polymerizing and drying the solution at a temperature above the boiling point of the solvent.

Abstract: A dry, solid, water-swellable absorbent composition of matter is prepared by blending together (a) a water-insoluble absorbent polymer and (b) from 1 to 75%, by weight of the blend, of an extender material selected from uncrosslinked cellulose derivatives, starch, certain clays and minerals, or mixtures thereof. The composition is characterized by having an absorbency exceeding the sum of the absorbencies, calculated proportionately, of the individual components. In one preferred embodiment, the absorbent polymer is a water-swellable ionic complex of a water-soluble anionic polyelectrolyte and a polyvalent metal cation having a valence of at least three.

Abstract: Homo- and copolymers of quaternary ammonium monomers are prepared directly in dry form by a process which comprises forming a solution of the monomer(s), solvent and a free-radical initiator and simultaneously polymerizing the monomers and drying the solution at a temperature above the boiling point of the solvent.

Abstract: Styrene and maleic anhydride monomers are copolymerized in 1,2-dichloroethane employing 3-mercaptopropionic acid or methyl-3-mercaptopropionate chain transfer agents producing an odorless copolymer in the molecular weight range of about 500 to 10,000 which remains soluble in the solvent. The resultant copolymer may be conveniently sulfonated in the 1,2-dichloroethane solvent used for the polymerization thereby producing an odorless sulfonated copolymer.

Abstract: Polystyrene and styrene copolymers are simultaneously crosslinked and sulfonated in a homogeneous reaction mixture by incorporation of from 0.1 to 5 mole percent of specific crosslinking reagents in the polymer sulfonating solution. The crosslinking reagents are selected aryl compounds having at least two --CH.sub.2 X radicals where X is hydroxyl, chlorine or bromine.

Abstract: Novel cationic starch-g-poly(N,N'-methylenebisacrylamide-co-amine) copolymers, useful as pigment retention aids for paper, are prepared by reacting a starch base with N,N'-methylenebisacrylamide and a polyamine or with preformed copolymer. The reactions are carried out at 15.degree. to 80.degree. C. for 0.5 to 20 hours under alkaline conditions using an aqueous slurry or dispersion of a starch base and preferably a salt such as sodium sulfate. The starch base may be derivatized, prior to the graft copolymerization, to introduce ether groups. The polyamines contain at least two amine groups selected from primary and secondary amines; preferably they contain up to 4 amine nitrogens, some of which may be unreactive tertiary amine nitrogens. The starch-g-coplymers are used in amounts of from about 0.05 to 2.0% by weight, based on the dry pulp. The reaction mixture itself may be added directly to the paper stock.

Abstract: Copolymerizable blocked isocyanate diols are prepared by reacting a blocking agent with an isocyanate group of an organic diisocyanate under controlled conditions, thereby forming a blocked isocyanate group, and reacting the second isocyanate group in a subsequent step with the amine portion of a selected amine diol under anhydrous conditions. The resultant products are used to prepare self-crosslinkable, linear polyurethanes of high molecular weight.

Abstract: Hot melt pressure sensitive adhesives are prepared by free-radical copolymerizing an acrylic-based comonomer(s) with allyl acrylate or methacrylate to produce a prepolymer with an ethylenically saturated backbone containing pendant allylic unsaturation which is then applied in fluid form to a substrate and thereafter subjected to electron beam curing.

Abstract: Dried, free-flowing powdered foodstuffs are produced from high fat containing foods by adding thereto a grinding agent comprising a food-grade film-forming material which has been spray-dried from solution in the presence of a latent gas and which is characterized by a bulk density within the range of 3 to 25 pounds per cubic foot and, additionally in the case of solid foodstuffs, grinding the mixture to effect powdering.

Abstract: Primer compositions useful in the cure of adhesive compositions containing acrylate and/or methacrylate monomers, chlorosulfonated polyethylene and a peroxy free radical generator comprise (a) the condensation product of an aldehyde and a primary or secondary amine and (b) a salt of a non-transition metal selected from the group consisting of lead, tin, zinc, calcium, strontium, barium and cadmium. These primers and the two part adhesives prepared therewith are characterized by superior speed of cure and final bond strength.

Abstract: A cold-water dispersible, modified starch characterized by forming a gel having a Bloom strength of at least 50 grams is prepared by reacting a tapioca starch with a crosslinking agent to within defined Brabender viscosity limits; converting the crosslinked starch in a sufficient amount to provide the modified starch with gelling properties; and drum-drying the crosslinked and converted starch to obtain the modified starch product. The gelling instant starch thus prepared is particularly useful in food systems of the type which gel upon standing, such as pie filling, jellies, and puddings.

Abstract: A cold-water dispersible, modified starch characterized by forming a gel having a Bloom strength of at least 60 grams is prepared by reacting a potato starch with a crosslinking agent to within defined Brabender viscosity limits sufficient to provide the modified starch with gelling properties and drum-drying the crosslinked starch to obtain the modified starch product. The starch may be optionally converted to a fluidity starch either before or after the crosslinking step and prior to drum drying. The gelling instant starch thus prepared is particularly useful in food systems of the type which gel upon standing, such as pie fillings, jellies, and puddings.

Abstract: The invention discloses a dual derivatizing process for the preparation of cold water swelling starches and foodstuffs thickened therewith. The starch base is first subjected to a primary crosslinking reaction using sodium trimetaphosphate (STMP) according to conventional techniques, then reslurried, treated with additional STMP and drum dried to effect a secondary crosslinking reaction in situ.