Abstract: This invention relates to a process for making an ion exchange material, the process comprising:(A) forming an aqueous solution comprising a water-soluble polymer containing pendent carboxyl groups and a water-soluble polyol, the number of carboxyl groups provided by said polymer being in excess of the number of hydroxyl groups provided by said polyol;(B) forming a thin film or a composite with the solution from step (A), the composite comprising the solution from step (A) in contact with a support material;(C) drying the solution to form a dried polymer;(D) heating the dried polymer from step (C) under esterification conditions to produce a water-insoluble partially esterified crosslinked polymer; and(E) contacting said partially esterified crosslinked polymer from step (D) with alkali or alkaline earth metal ions to form said ion exchange material.

Abstract: A bead is provided which consists essentially of peat moss immobilized by crosslinked neutralized poly(carboxylic acid) binder, sodium silicate binder, or polysulfone binder. The bead is effective to remove metal contaminants from dilute aqueous solutions. A method of making metal-ion-sorbing beads is provided, comprising combining peat moss or other nonliving biomass and binder solution (preferably in a pin mixer where it is whipped), forming wet beads, and heating and drying the beads. The binder solution is preferably poly(acrylic acid) and glycerol dissolved in water and the wet beads formed from such binder solution are preferably heated and crosslinked by radio frequency heating.

Abstract: The use of guanidine salts of organic fatty acids (guanidine soaps) as vehicles and binders for coating substrate surfaces is disclosed. Being completely organic, the guanidine soaps can be burned off leaving no undesirable residue. Of special interest is the use of guanidine 2-ethyl hexanoate as the vehicle and binder for coating problematic surfaces such as in coating alumina fibers with platinum or zirconia. For this application the guanidine soap is used as a melt. For other applications the guanidine soap may be used in a solution with a variety of solvents, the solution containing chlorometalates or powdered metals, refractories or ceramics.

Abstract: An ion exchange polymer comprised of an alkali metal or alkaline earth metal salt of a poly(carboxylic acid) in a poly(vinyl acetal) matrix is described. The polymer is made by treating a mixture made of poly(vinyl alcohol) and poly(acrylic acid) with a suitable aldehyde and an acid catalyst to cause acetalization with some cross-linking. The material is then subjected to an alkaline aqueous solution of an alkali metal salt or an alkali earth metal salt. All of the film forming and cross-linking steps can be carried out simultaneously, if desired.

Abstract: Guanidine oxalate is used as a precipitating agent in the coprecipitation of multicomponent oxide powder precursors. A solution of a soluble inorganic salt is combined with a solution of guanidine oxalate. A resultant metal oxalate is precipitated from the solution and can thereafter be subjected to heat to convert the metal oxalate into a multicomponent ceramic powder.

Abstract: The use of guanidine salts of organic fatty acids (guanidine soaps) as vehicles and binders for coating substrate surfaces is disclosed. Being completely organic, the guanidine soaps can be burned off leaving no undesirable residue. Of special interest is the use of guanidine 2-ethyl hexanoate as the vehicle and binder for coating problematic surfaces such as in coating alumina fibers with platinum or zirconia. For this application the guanidine soap is used as a melt. For other applications the guanidine soap may be use in a solution with a variety of solvents, the solution containing chlorometalates or powdered metals, refractories or ceramics.

Abstract: Guanidine oxalate is used as a precipitating agent in the coprecipitation of multicomponent oxide powder precursors. A solution of a soluble inorganic salt is combined with a solution of guanidine oxalate. A resultant metal oxalate is precipitated from the solution and can thereafter be subjected to heat to convert the metal oxalate into a multicomponent ceramic powder.

Abstract: Ceramic structures having high strength at temperatures above 1000.degree. C. after sintering are made by mixing ceramic powders with binder deflocculants such as guanidine salts of polymeric acids, guanidine salts of aliphatic organic caboxylic acids or guanidine alkylsulfates with the foregoing guanidine salts.

Abstract: A battery separator for an alkaline battery. The separator comprises a cross-linked copolymer of vinyl alcohol units and unsaturated carboxylic acid units. The cross-linked copolymer is insoluble in water, has excellent zincate diffusion and oxygen gas barrier properties and a low electrical resistivity. Cross-linking with a polyaldehyde cross-linking agent is preferred.

Abstract: A film-forming polyvinyl alcohol polymer is mixed with a polyaldehyde-polysaccharide cross-linking agent having at least two monosaccharide units and a plurality of aldehyde groups per molecule, preferably an average of at least one aldehyde group per monosaccharide units. The cross-linking agent, such as a polydialdehyde starch, is used in an amount of about 2.5 to 20% of the theoretical amount required to cross-link all of the available hydroxyl groups of the polyvinyl alcohol polymer. Reaction between the polymer and cross-linking agent is effected in aqueous acidic solution to produce the cross-linked polymer. The polymer product has low electrical resistivity and other properties rendering it suitable for making separators for alkaline batteries. In that event, the mixture of polymer and cross-linking agent is formed into a sheet or film or the like and the film is cut to size and otherwise fabricated into a configuration suitable for a particular end use.

Abstract: A method of producing a cross-linked polyvinyl alcohol structure, such as a battery separator membrane or electrode envelope. An aqueous solution of a film-forming polyvinyl alcohol is admixed with an aldehyde cross-linking agent at basic pH to inhibit cross-linking. The cross-linking agent, preferably a dialdehyde such as glutaraldehyde, is used in an amount of from about 1/2 to about 20% of the theoretical amount required to cross-link all of the hydroxyl groups of the polymer. The aqueous admixture is formed into a desired physical shape, such as by casting a sheet of the solution. The sheet is then dried to form a self-supporting film. Cross-linking is then effected by immersing the film in aqueous acid solution. The resultant product has excellent properties for use as a battery separator, including a low electrical resistivity, the value of which is principally determined by the amount of cross-linking which is easily and closely controlled by the amount of cross-linking agent added to the polymer.

Abstract: A self-supporting sheet structure comprising a water soluble, non-cross-linked polymer such as polyvinyl alcohol which is capable of being cross-linked by reaction with hydrogen atom radicals and hydroxyl molecule radicals is contacted with an aqueous solution having a pH of less than 8 and containing a dissolved salt in an amount sufficient to prevent substantial dissolution of the non-cross-linked polymer in the aqueous solution. The aqueous solution is then irradiated with ionizing radiation to form hydrogen atom radicals and hydroxyl molecule radicals and the irradiation is continued for a time sufficient to effect cross-linking of the water soluble polymer to produce a water-insoluble polymer sheet structure. The method has particular application in the production of battery separators and electrode envelopes for alkaline batteries.

Abstract: A battery separator is produced from a polyvinyl alcohol sheet structure which is subjected to an in situ, self cross-linking process by selective oxidation of the 1,2 diol units present in the polyvinyl alcohol sheet structure. The 1,2 diol units are cleaved to form aldehyde end groups which subsequently cross-link through acetalization of the 1,3 diol units of the polyvinyl alcohol. Selective oxidation is achieved using a solution of a suitable oxidizing agent such as periodic acid or lead tetraacetate.

Abstract: A process for the preparation and isolation of high purity anhydrous lower valence state metal halides comprising dissolving the corresponding higher valence state metal halide of the desired lower valence state metal halide in an organic liquid, which is selected such that the higher valence state metal halide is soluble therein and the lower valence state metal halide is insoluble therein, and subjecting the solution to high energy radiation which reduces the higher valence state metal halide to its corresponding lower valence state metal halide, at a temperature in the range of from about 0.degree.C. to about room temperature.

Abstract: This invention presents a method of making a rigid unitary fertilizer composite for fertilizing plants and trees and articles produced by the method. In the form of a spike, the composite has sufficient strength and toughness so as to enable it to be pushed or pounded into the ground near the roots of plants and trees. The method involves making an aqueous paste containing plant nutrients, acrylamide, and a catalyst for the polymerization of the acrylamide. The paste is then molded to the desired shape. The acrylamide is allowed to polymerize, after which time the excess water is removed by drying. The final product, which should contain at least 5 weight percent polyacrylamide, is a rigid mass.