Abstract: Water-displacing compositions based on fluorocarbon solvent FC-113 (1,1,2-trifluoro-1,2,2-trichloroethane) and certain surfactants are provided. These solutions serve to displace water from a broad range of substrates, including metals such as stainless-steel, aluminum alloys and brass, as well as from glass and ceramic surfaces such as lime glasses, borosilicate glass, unglazed alumina and fired alumina. In addition, these compositions do not form emulsions with the displaced water. This latter property is important to efficient water removal by decantation when the drying solvent is used in commercial drying processes and apparatus.The surfactants are chosen from a combination of: (a) the isopropyl amine salt of a dodecylbenzene sulfonic acid; (b) 2,4,7,9-tetramethyl-5-decyn-4,7-diol combined with an aliphatic primary alcohol in the range of hexanol to dodecanol; and (c) certain aliphatic esters of polyphosphoric acid, in the free-acid form.

Abstract: A process is described whereby gadolinium and gallium containing by-products can be reprocessed to yield the oxides of these elements in sufficient purity to be re-used in the process for manufacturing Gd.sub.3 Ga.sub.5 O.sub.12 (GGG) single crystal boules thereby improving the economics of production of GGG wafers significantly. The gadolinium and gallium oxides are recovered and separated from transition metal impurities introduced during fabrication of GGG wafers by precipitating the gadolinium as oxalate which is thereafter pyrolyzed to gadolinium oxide and eluting the gallium containing filtrate over an ion exchange resin and precipitating therefrom as an oxalate the gallium present. The gallium precipitate is also pyrolyzed to the gallium oxide. The process can be extended to include purification and re-use of by-products generated in other grinding and polishing operations which may result in the recycling of the order of 80% of the generated by-products.

Abstract: A process for preparing block, and/or graft copolymeric compositions by forming an intimate mixture of two or more polymers, at least one of which includes one or more amino junctions and at least one of the remaining polymers includes one or more carboxylic acid junctions and an effective amount of a phosphite compound, and thereafter heating the intimate mixture at a temperature and for a time sufficient to form the desired block, and/or graft copolymers.

Abstract: Formed from trifunctional units (M) having attached, to one of the two terminal carbon atoms of an alkylene hydrocarbon diradical, the functional group A', and having attached, to the other terminal carbon atom, a different functional group B' reactive with A' to form a linkage AB; and having attached, to a third carbon of the skeleton of unit (M), the functional group A" (preferably the same as A') reactive with B' whereby a macromolecule is built up of successive layers of units (M). The process involves successive stages in the first of which, the functional groups A' are blocked and group B is blocked with a "source" unit (S); then groups A' are liberated to form Compound I. In the second stage, Compound II is formed from the starting material (such as lysine) by first blocking groups A', then converting group B' to a form reactive with A'.

Abstract: A polymer composition having improved physical properties, and a method of preparing same.

Abstract: An electrodialytic distillative process for recovery of anhydrous hydrogen fluoride from an aqueous solution of fluosilicic acid and hydrogen fluoride wherein the concentration of hydrogen fluoride in said solution is such that hydrogen fluoride cannot be recovered therefrom by distillation, which comprises subjecting the solution to electrodialysis thereby increasing the total acids concentration in said solution to equal to or greater than about 46 weight percent, and thereafter recovering anhydrous hydrogen fluoride by distillation.

Abstract: Formed from trifunctional units (M) having attached, to one of the two terminal carbon atoms of an alkylene hydrocarbon diradical, the functional group A', and having attached, to the other terminal carbon atom, a different functional group B' reactive A' to form a linkage AB; and having attached, to a third carbon of the skeleton of unit (M), the functional group A" (preferably the same as A') reactive with B' whereby a macromolecule is built up of successive layers of units (M). The process involves successive stages in the first of which, the functional groups A' are blocked and group B is blocked with a "source" unit (S); then groups A' are liberated to form Compound I. In the second stage, Compound II is formed from the starting material (such as lysine) by first blocking groups A', then converting group B' to a form reactive with A'.

Abstract: This invention relates to fire retarded polymeric composition comprising a polymeric material, red phosphorus and a phosphine suppressant which is a copper salt.

Abstract: Partially unsaturated polymers are dissolved in a two component solvent comprising a first component having a reactivity toward ozone less than carbon-carbon double bonds but more reactive than carbon-carbon single bonds and a second component being inert toward ozone. Introduction of ozone into the solution produces ozonides which are readily cleft into difunctional aliphatic species that can be converted to e.g. carboxy-terminated or multifunctional carboxy substituted aliphatic compounds. These may be used as monomeric species in various polymerization schemes as such, in preparation of polyamides, for example, or may be reduced to aldehydes or alcohols to be used in the preparation of such polymers as polyesters, polyurethanes, poly (Schiff bases), etc. The carboxylated products may also be employed as ionomers, which are useful as surfactants. Monocarboxyl terminated polyethylene having a number average molecular weight of from about 4,000 to 100,000 are provided.

Abstract: A polyester based composition comprising sodium citrate as a nucleating agent.

Abstract: Aqueous phosphoric acid solutions containing uranium values are contacted with an organic solution of a mixture of organophosphorus compounds produced from a carboxylic acid and PCl.sub.3 in the presence of water or from corresponding acid halides or anhydrides and phosphorous acid to extract the uranium values. The organophorus compounds generally include an alkane-1,1,2-triphosphonic acid or a 1-hydroxy-1,1-alkanediphosphonic acid or both, which differ from common organophosphorus extractants in having a carbon-phosphorus bond. The extraction has high distribution coefficients even when the phosphoric acid solution is 10 molar or more and even when the extraction is conducted at elevated temperatures such as 60.degree. C. While distribution coefficients in the presence of iron are higher for tetravalent uranium, efficient extraction can be conducted of hexavalent uranium as well.