Abstract: An extractive distillation process is provided for the separation of phenol and/or cresol from mixtures with high boiling oxygenated compounds such as alkanols, alkanones, cycloalkanones, cycloalkanols, aryl alcohols, aryl ketones or mixtures thereof that have a boiling point of at least about 175.degree. C. The process involves distilling the phenol and/or cresol-high boiling oxygenated compound mixture in the presence of at least one extractive solvent comprising a substituted phenol and/or substituted cresol that has a boiling point between about 195.degree. C. and about 400.degree. C.

Abstract: A process for the production of oligomeric mixtures useful as surfactants is disclosed. The initial step of the process comprises reacting pyromellitic dianhydride with a fluoroalcohol using a mole ratio of about one mole pyromellitic dianhydride per two moles of fluoroalcohol to produce an intermediate which contains two fluorinated ester moieties and two free acid moieties. Thereafter, the intermediate diester-diacid is reacted with an excess of an oxirane compound such as epichlorohydrin, epibromohydrin or propylene oxide wherein said oxirane compound reacts with the free acid moieties to produce ester moieties containing a primary or secondary alcohol moiety. In the final step of the process, additional pyromellitic dianhydride is added to the reaction mixture so that the alcohol moieties may react with anhydride moieties to produce ester linking groups (between pyromellitate nuclei) and additional free acid moieties capable of reacting with the oxirane compound.

Abstract: Purified aromatic dicyanates are cured with a catalyst which is an Mn(II), Ag(II), Fe(III), Bi(III), In(III) or Hf(IV) salt at 150.degree.-200.degree. C. and then at 200.degree.-300.degree. C. for a time sufficient to cure the dicyanate without causing color formations to the extent of a Yellowness Index over 30. In some forms the dicyanate is combined with the catalyst and a thermoplastic.

Abstract: Solutions of ultrahigh molecular weight polymers such as polyethylene in a relatively non-volatile solvent are extruded through an aperture at constant concentration through the aperture and cooled to form a first gel of indefinite length. The first gels are extracted with a volatile solvent to form a second gel and the second gel is dried to form a low porosity xerogel. The first gel, second gel or xerogel, or a combination, are stretched. Among the products obtainable are polyethylene fibers of greater than 30 or even 40 g/denier tenacity and of modulus greater than 1000 or even 1600 or 2000 g/denier.

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 process for preparing substituted or unsubstituted benzoxazoline compound by reacting ammonia, a cycloalkanone and oxygen in the presence of metal cations.

Abstract: Tetraesters of pyromellitic dianhydride are disclosed wherein two ester moieties are saturated hydrocarbon groups and two ester moieties are halohydroxyalkyl groups. The compounds may be used as diluents for fluorinated pyromellitates that are useful as soil and water repelling agents. Mixtures formed by dissolving the compounds of this invention and known fluorinated pyromellitates in a common solvent are capable of imparting soil and water repelling properties to various fibers that are essentially equivalent to soil and water repelling properties imparted to such fibers by fluorinated pyromellitates alone. Additionally, the hydrocarbon pyromellitates of this invention may be used alone as water repellents.

Abstract: Benzene, or an alkylbenzene, is hydrogenated by reaction with hydrogen in the presence of a Group IVa (titanium family) or Va metal hydride catalyst. The catalyst may be a simple hydride such as ZrH.sub.2 or a hydride of an alloy such as Cu.sub.3 Zr or may be a complex material. One complex material is the reaction product of a Group IVa or Va metal halide, such as ZrCl.sub.4 with an alkyllithium or aryllithium, such as n-butyllithium, in a hydrocarbon solvent.

Abstract: Silicon tetrafluoride is reacted with sodium hydride in a cyclic ether reaction medium such as tetrahydrofuran or 1,4-dioxane or in dimethoxyethane. Sodium aluminum hydride is dissolved in the solvent and catalyzes the reaction in amounts of 4-25%, by weight of combined sodium hydride and sodium aluminum hydride.

Abstract: Electrically conducting polyacetylene compositions are described having incorporated therein a fluorine-containing peroxide, such as FSO.sub.2 --O--O--SO.sub.2 F. Preferred compositions exhibit novel metal-like conductivity at temperatures above about 150.degree. K., and specific conductivities above about 10.sup.2 ohm.sup.-1 -cm.sup.-1 at room temperature, as measured by the standard four-probe method. A process for producing the compositions is also described in which polyacetylene is contacted with the peroxide, preferably in an inert liquid solvent at low temperatures.

Abstract: Articles such as vests, helmets and structural elements containing a network of ultrahigh molecular weight, high strength, high modulus polyethylene or polypropylene fibers. The fibers, and especially polyethylene fibers of 15, 20, 25, 30 or more g/denier tenacity, and 300, 500, 1000, 1500 or more g/denier tensile modulus impart exceptional ballistic resistance to the articles in spite of the melting points, e.g. 145.degree.-151.degree. C. for the polyethylene fibers and 168.degree.-171.degree. C. for the polypropylene fibers, which are high for these polymers, but substantially lower than the 200.degree. C. or more melting point previously thought necessary for good ballistic resistance.

Abstract: A flame retarded, injection moldable, saturated, linear polyester composition contains red phosphorus as flame retardant and a metal iodide as phosphine suppressing agent. The metal is one of the groups 1a and 2b of the periodic table of elements with potassium iodide being the most preferred.The phosphine evolution of a poly(ethylene terephthalate) molding composition containing 4% red phosphorus as flame retardant is reduced to 0.3 ppm at the die and to 1.0 ppm in storage by the addition of 0.6% of potassium iodide.

Abstract: Uranium is extracted from phosphoric acid with organophosphorus extractants supported or impregnated on polymeric resins, and especially macroreticular resins. Suitable extractants include mono and dialkylphenyl esters of phosphoric acid. Uranium may be stripped from the supported or impregnated resins with hotter or more concentrated phosphoric acid, optionally with oxidation to hexavalent form, or with aqueous fluoride solutions.

Abstract: A Group IVa metal halide such as methyl trichlorosilane is reacted with an oxime compound such as methyl ethyl ketone oxime in the absence of a base to form in high yields a product oximinosilane, oximinogermane or oximinostannane (e.g. methyl tris(methyl ethyl ketoximo)silane) and a by-product oxime hydrohalide. The oxime above that found in the product may be recovered by neutralization of the by-product oxime hydrohalide.

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

Abstract: A thermotropic poly(ester carbonate) containing diacyl moieties such as terephthalate and carbonate moieties as well as dihydroxy-derived moieties is useful for forming fibers or films. The dihydroxy-derived moieties are at least 40% derived from t-butylhydroquinone, with hydroquinone and methylhydroquinone being exemplary second components. The polymers can be prepared by melt, solution or interfacial polymerization, are liquid crystalline in the melt and have glass transition temperatures above 100.degree. C.

Abstract: Dialkoxyketoximes such as dimethoxycyclohexanone cleave with halogen and water under basic conditions to yield a series of products having an ester functionality and another functionality which is oximohalide, nitrile oxide or furoxan, depending upon the base strength and/or work-up conditions. Each of those products can be further reacted with sulfur dioxide to produce an adduct, from which an isocyanate is derived. Both the adduct and the isocyanate retain the ester functionality.

Abstract: The subject polymers are novel homopolymers and copolymers. The homopolymers are characterized by relatively high T.sub.g of about 120.degree. C. relative to their T.sub.m of about 250.degree. C., whereby they can readily be fabricated into fibers, films and like structures from the melt, and retain strength above 100.degree. C. The copolymers have T.sub.g 's intermediate between those of the homopolymers of the constituent monomers, and can be fabricated as for the subject homopolymers.Novel processes of obtaining the monomer, p-(1,1-dimethyl-2-hydroxyethyl)benzoic acid, are disclosed.

Abstract: A two-compartment water splitter having alternating cation and bipolar membranes is used to remove alkali metal cations from an aqueous alkali metal chloride solution so as to produce an acidified salt solution. The coproduct is a base such as NaOH or KOH. The acidified salt solution may then be fed to a membrane or diaphragm electrolytic cell for production of chlorine and alkali metal hydroxide.

Abstract: A molding composition of a terephthalate polyester such as PET, a plasticizing material and a crystal nucleating agent. The nucleating agent is a powdered metal hydroxide such as aluminum hydroxide, which raises the T.sub.cc of the composition and permits reduced cycling time and enables higher molecular weight polymer to be used in the molding process.