Abstract: This invention provides thermally stable urea-sulfuric acid compositions and methods for manufacturing and using such compositions. The novel compositions comprise combinations of urea and sulfuric acid which contain less than about one weight percent water based on the combined weight of urea and sulfuric acid. Such compositions are substantially more stable thermally than are compositions which contain more than about one weight percent water.The thermally stable compositions are prepared by forming the urea-sulfuric acid component in the presence of less than one weight percent water based on the combined weight of urea and sulfuric acid and/or by physically and or chemically removing water from the urea-sulfuric acid component. Water can be removed by evaporation and/or by contacting the urea-sulfuric acid component, either during or after its formation, with one or more chemical dehydrating agents capable of chemically combining with water in the composition.

Abstract: Cellulosic materials are physically and/or chemically modified by contact with a combination of urea and sulfuric acid in which at least 25 percent of the sulfuric acid is present as the monourea adduct of sulfuric acid. The cellulosic materials thus treated possess uniquely modified physical and chemical properties. The methods of the invention can be employed to weaken the physical structure of the cellulosic material and thereby to assist in clearing land of vegetation and vegetation residue and in compacting and other processing of waste cellulosic materials. The methods of the invention can also be employed to increase the food value of cellulosic materials for animals, including humans, and, in particular, to increase the food value of such materials for ruminant mammals.

Abstract: Plant seeds are beneficiated by contacting them with an aqueous solution of a urea-sulfuric acid component containing the monourea adduct of sulfuric acid. The molar ratio of urea to sulfuric acid in the aqueous solution is preferably within the range of about 1/4 to about 7/4 so that at least about 25 percent of the sulfuric acid is present in the solution as the monourea adduct. The treatment of plant seeds with the aqueous urea-sulfuric acid components is particularly useful for removing residual plant matter from plant seeds, scarifying and improving the germination of plant seeds, and improving the processability and digestibility of plant seeds. Improvements in processability result from softened seed hulls or husks, improved extractability of oil from oil-containing seeds, and improved quality of treated seeds for the manufacture of seed derived products, particularly for the manufacture of grain-derived products.

Abstract: Plant seeds are beneficiated by contacting them with an aqueous solution of a urea-sulfuric acid component containing the monourea adduct of sulfuric acid. The molar ratio of urea to sulfuric acid in the aqueous solution is preferably within the range of about 1/4 to about 7/4 so that at least about 25 percent of the sulfuric acid is present in the solution as the monourea adduct. The treatment of plant seeds with the aqueous urea-sulfuric acid components is particularly useful for removing residual plant matter from plant seeds, scarifying and improving the germination of plant seeds, and improving the processability and digestibility of plant seeds. Improvements in processability result from softened seed hulls or husks, improved extractability of oil from oil-containing seeds, and improved quality of treated seeds for the manufacture of seedderived products, particularly for the manufacture of grain-derived products.

Abstract: Compositions containing sulfuric acid and one or more of certain chalcogen-containing compounds in which the chalcogen compound/H.sub.2 SO.sub.4 molar ratio is below 2 contain the mono-adduct of sulfuric acid which is catalytically active for promoting organic chemical reactions. Suitable chalcogen-containing compounds have the empirical formula ##STR1## wherein X is a chalcogen, each of R.sub.1 and R.sub.2 is independently selected from hydrogen, NR.sub.3 R.sub.4, and NR.sub.5, at least one of R.sub.1 and R.sub.2 is other than hydrogen, each of R.sub.3 and R.sub.4 is hydrogen or a monovalent organic radical, and R.sub.5 is a divalent organic radical. Such compositions are useful for catalyzing organic reactions such as oxidation, oxidative addition, reduction, reductive addition, esterification, transesterification, hydrogenation, isomerication (including racemization of optical isomers), alkylation, polymerization, demetallization of organometallics, nitration, Friedel-Crafts reactions, and hydrolysis.

Abstract: Certain urea-sulfuric acid components, comprised of urea and sulfuric acid in a 1/4 to 7/4 molar ratio, contain a monourea adduct of sulfuric acid, which is catalytically active for promoting organic chemical reactions. The invention provides methods employing such urea-sulfuric acid components for catalyzing organic reactions such as oxidation, oxidative addition, reduction, reductive addition, esterification, transesterification, hydrogenation, isomerization (including racemization of optical isomers), alkylation, polymerization, demetallization of organometallics, nitration, Friedel-Crafts reactions, and hydrolysis. Novel catalysts are disclosed which involve combinations of the urea-sulfuric component with one or more transition metal halides and/or with one or more surfactants. The surfactant-containing compositions are particularly useful for the treatment of materials containing lipophilic substances.

Abstract: Compositions containing sulfuric acid and one or more of certain chalcogen-containing compounds in which the chalcogen compound/H.sub.2 SO.sub.4 molar ratio is below 2 contain the mono-adduct of sulfuric acid which is catalytically active for promoting organic chemical reactions. Suitable chalcogen-containing compounds have the empirical formula ##STR1## wherein X is a chalcogen, each of R.sub.1 and R.sub.2 is independently selected from hydrogen, NR.sub.3 R.sub.4, and NR.sub.5, at least one of R.sub.1 and R.sub.2 is other than hydrogen, each of R.sub.3 and R.sub.4 is hydrogen or a monovalent organic radical, and R.sub.5 is a divalent organic radical. Such compositions are useful for catalyzing organic reactions such as oxidation, oxidative addition, reduction, reductive addition, esterification, transesterification, hydrogenation, isomerication (including racemization of optical isomers), alkylation, polymerization, demetallization of organometallics, nitration, Friedel-Crafts reactions, and hydrolysis.

Abstract: Additives comprising an adduct of a calcium salt of a thiocarbonic acid and calcium hydroxide are useful in lubricants to enhance both the extreme pressure/anti-wear and anti-oxidation capabilities thereof. The lubricants are preferably oils of lubricating viscosity, which may be thickened to a grease-like consistency with one or more oil thickeners and contain from about 0.1 to about 20 weight percent of said adduct.

Abstract: Additives comprising a salt or complex of tetrathiocarbonic acid are useful in lubricants to enhance both the extreme pressure/anti-wear and anti-oxidant capabilities thereof. The lubricants preferably are oils of lubricating viscosity, which may be thickened to grease-like consistency with one or more oil thickeners, and contain from about 0.1 to about 20 weight percent of said additives.

Abstract: Additives containing a salt or complex of trithiocarbonic acid are useful in lubricants to enhance the extreme pressure/anti-wear and anti-oxidation capabilities thereof. The lubricants are preferably oils of lubricating viscosity, which may be thickened to a grease-like consistency with one or more oil thickeners, and contains from about 0.1 to about 20 weight percent of said additives.

Abstract: Textile materials having improved physical properties comprise woven and/or non-woven fiber assemblies, the fibers of which are bound to a polymer composition containing polymerized carboxylic acid ester monomers and pendant functional groups attached to a polymer backbone and having the formula: ##STR1## in which R.sub.1 is a divalent organic radical at least 3 atoms in length, and X is organoacyl or cyano. Such polymers markedly increase wet and dry strengths and shape retention of textile materials, and they improve other physical properties without the necessity of employing formaldehyde-releasing monomers, such as the N-methylolamides, or cross-linking agents. Methods for producing such textile materials by applying solutions or dispersions of the described polymers to fiber assemblies are also provided. Aqueous dispersions of these polymers are particularly useful for the manufacture of loose-weaves, kints and non-wovens.

Abstract: Compositions containing sulfuric acid and one or more of certain chalcogen-containing compounds in which the chalcogen compound/H.sub.2 SO.sub.4 molar ratio is below 2 contain the mono-adduct of sulfuric acid which is catalytically active for promoting organic chemical reactions. Suitable chalcogen-containing compounds have the empirical formula ##STR1## wherein X is a chalcogen, each of R.sub.1 and R.sub.2 is independently selected from hydrogen, HR.sub.3 R.sub.4, and NR.sub.5, at least one of R.sub.1 and R.sub.2 is other than hydrogen, each of R.sub.3 and R.sub.4 is hydrogen or a monovalent organic radical, and R.sub.5 is a divalent organic radical. Such compositions are useful for catalyzing organic reactions such as oxidation, oxidative addition, reduction, reductive addition, esterification, transesterification, hydrogenation, isomerication (including racemization of optical isomers), alkylation, polymerization, demetallization of organometallics, nitration, Friedel-Crafts reactions, and hydrolysis.

Abstract: Compositions containing sulfuric acid and one or more of certain chalcogen-containing compounds in which the chalcogen compound/H.sub.2 SO.sub.4 molar ratio is below 2 contain the mono-adduct of sulfuric acid whci is catalytically active for promoting organic chemical reactions. Suitable chalcogen-containing compounds have the empirical formula ##STR1## wherein X is a chalcogen, each of R.sub.1 and R.sub.2 is independently selected from hydrogen, NR.sub.3 R.sub.4, and NR.sub.5, at least one of R.sub.1 and R.sub.2 is other than hydrogen, each of R.sub.3 and R.sub.4 is hydrogen or a monovalent organic radical, and R.sub.5 is a divalent organic radical. Such compositions are useful for catalyzing organic reactions such as oxidation, oxidative addition, reduction, reductive addition, esterification, transesterification, hydrogenation, isomerication (including racemization of optical isomers), alkylation, polymerization, demetallization of organometallics, nitration, Friedel-Crafts reactions, and hydrolysis.

Abstract: L-(d)-lactic acid, the dextrorotatory isomer of lactic acid, is an effective plant growth regulant which exhibits classical growth regulant activity at very low concentrations and dosage rates. It can be employed to beneficially stimulate the growth of all plant varieties and is particularly useful for stimulating the growth of commercial crops. As is the case with other growth regulants, L-lactic acid can also be employed to inhibit the growth of plants when applied at sufficiently high concentrations. Thus, L-lactic acid can be employed to stimulate the growth of desired plants, to stimulate the fruit production of fruit-bearing plants, and to inhibit the growth of undesired vegetation. Novel compositions which comprise mixtures of L-(d)-lactic acid and one or more preservatives which are sufficient to prevent the hydrolytic and/or bacterial decomposition of the active isomer are also disclosed.

Abstract: Permanently flexible and non-tacky coating mastic and caulking compositions contain one or more polymers having a T.sub.g of about -50.degree. C. to about -10.degree. C. and pendant functional groups attached to the polymer backbone of the formula: ##STR1## in which R.sub.1 is a divalent organic radical at least 3 atoms in length, and X is organoacyl or cyano. The mastics and caulks typically have total non-volatile matter concentrations of about 60 to about 90 weight percent of which about 15 to about 75 weight percent comprises the described polymers and about 25 to about 85 weight percent is non-volatile solid matter other than the polymer such as pigments, fillers, etc.

Abstract: Vanadium is recovered from vanadium-containing phosphoric acid solutions by adjusting the pH so as to convert the dissolved vanadium to a simple vanadate compound which is insoluble in the phosphoric acid solution at the adjusted pH and separating the resulting insoluble simple vanadate compound from the phosphoric acid solution. The vanadium dissolved in the phosphoric acid solution can be converted to insoluble simple vanadates by reaction with oxidants and/or cations which form phosphoric acid-insoluble simple vanadates. These methods can be employed to selectively recover vanadium from phosphoric acid solutions containing other metals. They also can be employed to recover vanadium compounds from ores, scrap metal, and other vanadium sources by dissolving the vanadium from the vanadium source in phosphoric acid and recovering the vanadium as an insoluble simple vanadate from the phosphoric acid as described.

Abstract: Polysaccharides are at least partially hydrolyzed by contact with a composition containing urea, sulfuric acid, and water in which the urea/sulfuric acid molar ratio is less than 2. Such proportions of urea and sulfuric acid assure the presence of the monourea adduct of sulfuric acid. The polysaccharide can be hydrolyzed to an extent sufficient only to hydrate the polysaccharide to produce a hydrated polysaccharide such as hydrated cellulose, or it can be completely hydrolyzed to its constituent monosaccharides. Thus, cellulose can be converted to glucose.

Abstract: Plant seeds are beneficiated by contacting them with an aqueous solution of a urea-sulfuric acid component containing the monourea adduct of sulfuric acid. The molar ratio of urea to sulfuric acid in the aqueous solution is preferably within the range of about 1/4 to about 7/4 so that at least about 25 percent of the sulfuric acid is present in the solution as the monourea adduct. The treatment of plant seeds with the aqueous urea-sulfuric acid components is particularly useful for removing residual plant matter from plant seeds, scarifying and improving the germination of plant seeds, and improving the processability and digestibility of plant seeds. Improvements in processability result from softened seed hulls or husks, improved extractability of oil from oil-containing seeds, and improved quality of treated seeds for the manufacture of seed-derived products, particularly for the manufacture of grain-derived products.

Abstract: Pests are controlled by applying to the location of and/or to the path traversed by the pests a composition comprising urea and sulfuric acid in which the urea H.sub.2 SO.sub.4 molar ratio is less than 2. Novel compositions useful in such methods are also provided and comprise the described combinations of urea and sulfuric acid dispersed in a hydrocarbon oil. The novel method and compositions are particularly useful for controlling plant pests by applying the useful urea-sulfuric acid components to the plants or to the vicinity of plants occupied or tranversed by such pests.

Abstract: The growth of microorganisms in stored crops, and especially in animal feedstuffs, is inhibited by the application of a preservative composition which comprises ammonia, urease enzyme urea and/or urea polymers in a fluid medium. Urea polymers which are useful include biuret, triuret, cyanuric acid, urea cyanurate and other compounds which decompose to form ammonia. The effect of treatment with the preservative composition is to provide an immediate microorganism-inhibiting ammonia level, which, due to delayed decomposition of the urea and urea polymers, is sustained to some significant degree during prolonged storage of the treated material.