Abstract: The process for converting feed materials of high mineral content containing primary metal values and fluorine values to the primary metal or useful compounds thereof and to fluorine values or useful compounds thereof, wherein the feed materials constitutes a difficultly soluble matrix, the process having the steps of contacting the feed materials in a reactor with a humidified, gaseous system at from about 200.degree. C. to about 1600.degree. C., the contacting being carried out such as to convert the primary metal values to oxide residues at commercially acceptable rates and to evolve gaseous fluoride from the feed, digesting said oxide residues in an acidic digest medium and separating the primary metal values from the resulting digest liquor and from other components of the residues.

Abstract: An infants pacifier and medicine administering unit having a generally shield-shaped body with first and second sides and having an aperture extending therethrough around a generally transverse axis. The aperture being defined by a first wall. A flexible nipple having an inlet and a sucking orifice spaced therefrom, and a substantially sealed, compressible fluid dispenser having an outlet being mounted on opposite sides of the body with the inlet and the outlet being juxtaposed for fluid communication with each other thru a pressure openable valve whereby fluid in the dispenser can be injected under pressure into the nipple.

Abstract: Compositions comprising polyester or polycarbonate having reacted therein a total of from about 1.0 to about 5,000 parts by weight per million parts by weight of polyester of at least one UV absorbing compound of the formula ##STR1## wherein R is alkyl or the like, X is carbonyl or sulfonyl, R.sup.1 is hydrogen or a substituent, and Y and Z are hydrogen or substituents such as cyano or alkoxycarbonyl, with the provision that at least one of R, R.sup.1, Y, and Z is, or forms part of, or contains one or more reactive groups capable of undergoing a condensation reaction under polyester forming conditions, such that the UV absorbing compound is reacted into the polymer. The compound has a maximum light absorbance within the range of from about 320 nm to about 380 nm, which is nonextractable from the polyester and stable under the polyester processing conditions, for imparting UV screening properties to the polymer.

Abstract: The present invention relates to a novel acrylic composition, novel acrylic castings prepared therefrom, and a novel process for the preparation of the acrylic castings. The composition comprises methyl methacrylate, about 0.5 to 20% by weight of a carboxylated cellulose ester, and about 1 to 100 ppm of a vanadium promoter. Optionally, a heat dissipative material, such as a plasticizer or an additional monomer, can also be employed. In accordance with the process of the present invention, an acrylic monomer comprising methyl methacrylate is combined with about 0.5 to 20% by weight of a carboxylated cellulose ester so as to form an easily pourable syrup, about 1 to 100 ppm of a vanadium promoter is added to the syrup and the resulting solution is poured into a suitable mold, and the solution is cured at room temperature so as to form a hard acrylic casting.

Abstract: Compounds of the formula ##STR1## and their preparation wherein R.sup.1 and R.sup.2 are each selected from H and alkyl wherein the alkyl moieties are straight or branched chain of 1-20 carbons, preferably 1-6 carbons. Readily prepared therefrom are the corresponding unsaturated esters of the formula R.sup.2 S(R.sup.1)CH--CH.sub.2 --CH.dbd.CH--COO-alkyl which are useful as intermediates in the preparation of herbicides.

Abstract: Molding or fiber grade condensation polymer having copolymerized therein a total of from 1.0 to about 5,000 ppm of at least one methine moiety having one or more methine units defined as "the group >C.dbd.C< conjoined with a conjugated aromatic system," said moiety absorbing in the range of from about 350 nm to about 650 nm, and being nonextractable from said polymer and stable under the polymer processing conditions. The moieties preferably have molecular weights of from about 200 to about 600 although lower and higher molecular weights are also operable and are derived from reactants (monomers) having one or more groups such as hydroxyl, carboxyl, carboxylic ester, acid halide, amino and the like which condense during condensation or polycondensation to enter the moiety into the polymer chain.

Abstract: Polyester compositions useful in formed articles such as beverage bottles and having condensation reacted therein at least one UV-absorbing compound of the formula ##STR1## wherein: R is hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, cycloalkyl, substituted cycloalkyl, or alkenyl;R.sup.1 is hydrogen, or alkyl, aryl, or cycloalkyl, all of which may be substituted;R.sup.2 is hydrogen, or alkyl, cycloalkyl or aryl, all of which may be substituted;R.sup.3 is hydrogen or 1-3 substituents; andP is cyano or a group such as carbamoyl, aryl, alkylsulfonyl, arylsulfonyl, alkanoyl or aroyl, all of which groups may be substituted;whereby the polyester composition has maximum light radiation absorbance within the range of from about 320 nm to about 380 nm.

Abstract: A process for removing iron pentacarbonyl from carbon monoxide feed gas, comprising contacting the gas with a removal agent comprising alkali metal hydroxide in association with a high boiling hydroxylic solvent to form a nonvolatile iron carbonylate salt, and separating the gas from said agent and the salt. Preferably, the removal agent is adsorbed on a porous support such as diatomaceous earth at a concentration of from about 1% to about 40% by weight of the support, and the solvent is selected from one or mixtures of ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, 2,2,4-trimethyl-1,3-pentanediol, glycerine, triethanolamine, 1,4-butanediol, 1,2-propanediol, 1,3-butanediol, 2,5-hexanediol, 1-hexanol and 2-hexanol.

Abstract: The present invention relates to novel graft copolymers and to a novel process for the preparation thereof. The polymeric compositions provided by the present invention comprise the reaction product of an ethylenically unsaturated monomer and a carboxylated cellulose ester having an acid number of at least about 5, an inherent viscosity of from about 0.01 to about 1.00 and wherein the anhydroglucose units thereof have ring substituents comprising by weight based on total polymer weight, of from about 0.05 to about 20% hydroxyl groups, from about 0.5 to about 44% acetyl groups, from 0 to about 54% butyryl groups, from 0 to about 47% propionyl groups, from about 0.4 to about 4.0% total carboxyl groups wherein from about 20% to about 100% of these carboxyl groups are non-saponifiable backbone, and wherein the material has a lactone level of from about 4.52.times.10.sup.-15 to about 6.13.times.10.sup.-4.

Abstract: The present invention relates to a novel acrylic composition, novel acrylic castings prepared therefrom, and a novel process for the preparation of the acrylic castings. The composition comprises methyl methacrylate, about 0.5 to 20% by weight of a carboxylated cellulose ester, and about 1 to 100 ppm of a vanadium promoter. Optionally, a heat dissipative material, such as a plasticizer or an additional monomer, can also be employed. In accordance with the process of the present invention, an acrylic monomer comprising methyl methacrylate is combined with about 0.5 to 20% by weight of a carboxylated cellulose ester so as to form an easily pourable syrup, about 1 to 100 ppm of a vanadium promoter is added to the syrup and the resulting solution is poured into a suitable mold, and the solution is cured at room temperature so as to form a hard acrylic casting.

Abstract: The present invention provides a process for the selective production of ketones under hydroformylation conditions. In particular, the process comprises the hydroformylation of at least one olefin in the presence of hydrogen, carbon monoxide, and a catalyst which consists essentially of triruthenium dodecacarbonyl. The olefin preferably comprises propylene. The reaction is conducted under conditions such that the ratio of olefin:ruthenium is about 200:1 to 3000:1, the ratio of carbon monoxide:hydrogen:olefin to about 1:1.4:4 to 1:6:100, the total pressure is about 500 to 10,000 psig, the carbon monoxide partial pressure is about 50 to 500 psig, and the reaction temperature is about 60.degree. to 250.degree. C.

Abstract: Poly(urea-amides) having an inherent viscosity (I.V.) of 0.4 to about 1.2, and having the repeating units ##STR1## wherein with respect to the total moles of II and III, the mol % of II is 5 to 80, preferably 20 to 60, and conversely the mol % of III is 20 to 95, preferably 40 to 80, R is straight chain alkylene of 3 to 10 carbons, preferably 4 carbons, with the proviso that when R contains 3 carbons, not over 50 mol % thereof is present, up to 40 mol %, preferably 0 mil % of R is aromatic, and wherein up to 30 mol %, preferably 0 mol % of I is the para isomer, the remainder being the meta isomer, are valuable for the manufacture of plastics, fibers, films and other shaped objects, especially multilayer laminated structures which have excellent resistance to the transmission of oxygen, carbon dioxide, and other gases.

Abstract: Poly(ethylene terephthalate), poly(1,4-cyclohexanedicarboxylate), poly(ethylene isophthalate), poly(ethylene naphthalate), their copolymers with each other and with modifying aliphatic dicarboxylic acids, and substituted glycol repeat unit modifications thereof are produced from prepolymer (oligomer) obtained from the esterification of the acid or acids with ethylene carbonate or substituted ethylenecarbonate in the presence of one or more amines compounds selected from trialkylamines, tetraalkyldiamines, N-alkylated heterocyclic amines, and certain quaternary ammonium salts, employing certain mole ratios of ethylene carbonate and substituted ethylene carbonate to the diacid. The prepolymer is formed in an unusually short time and the final polyester of high I.V. exhibits improvement in such properties as desirable light color and low ether-glycol level.

Abstract: Disclosed are new disperse azo dyes prepared from 2-amino-cinnamoylthiophene compounds. These dyes give bright blue shades, for example, on polyester, cellulose acetate and other synthetic fibers and exhibit improvements in one or more of such properties as bathochromic shift, fastness to light, sublimation, chlorine, heat, ozone, gas, perspiration, crock, and wash, build, pH stability, bloom resistance, depth of shade, leveling, strike rate, migration, and the like. The dyes have the general formula: ##STR1## wherein each R is a substituent selected for example from alkyl, substituted alkyl, hydroxy, alkoxy, halogen, nitro, alkoxycarbonyl, alkanoyloxy, alkanoyl, cyano, alkylamino, and dialkylamino, R.sup.14 is hydrogen or alkyl, C.sup.1 represents an aniline, tetrahydroquinoline or benzomorpholine coupling component which may be extensively substituted, and each of R.sup.12 and R.sup.13 is hydrogen or a substituent such as acyl, acylamido, alkyl, halogen, and cyano.

Abstract: Disclosed are azo dyes containing diazonium moieties from aminothiazoles, aminoisothiazoles, or aminothiadiazoles (1,2,4- or 1,3,4-), and certain coupler moieties from aniline, tetrahydroquinoline, and benzomorpholine type compounds, wherein the diazonium moieties have at least one cinnamoyl group, and wherein a wide variety of groups, e.g., one or more water-solubilizing substituents such as sulfonic acid groups or their metal or amine salts may be present in the dye molecule. These dyes are useful for dyeing materials selected from polyamide, cellulose ester, polyester, wool and other natural and synthetic fibers and generally exhibit improvements in dyeability and fastness properties.

Abstract: The present invention provides a novel cellulosic material and a process for preparing the same. The cellulosic material is a carboxylated cellulose ester material having an acid number of at least about 5, an inherent viscosity of from about 0.01 to about 1.00 and wherein the anhydroglucose units thereof have ring substituents comprising by weight based on total polymer weight, of from about 0.05 to about 20% hydroxyl groups, from about 0.5 to about 44% acetyl groups, from 0 to about 54% butyryl groups, from 0 to about 47% propionyl groups, from about 0.4 to about 4.0% total carboxyl groups wherein from about 20% to about 100% of these carboxyl groups are non-saponifiable backbone, and wherein the material has a lactone level of from about 4.52.times.10.sup.-5 to about 6.13.times.10.sup.-4. The carboxylated cellulose esters of the present invention are prepared by reacting a cellulose ester with ozone at a temperature of about 25.degree. to 80.degree. C.

Abstract: A hydroformylation process for producing relatively low ratios of normal to branched aldehyde product, wherein olefin having from 2 to 20 carbons, preferably 3-10 carbons, and most preferably one or more of ethylene, propylene and 1-butene is contacted in a reaction zone at a temperature of from about 60.degree. C. to about 250.degree. C., preferably from about 150.degree. C. to about 200.degree. C., and a pressure of from about 750 psig to about 10,000 psig, preferably from about 3,000 psig to about 4,000 psig, with hydrogen and carbon monoxide, in the presence of a catalyst containing from about 10.sup.-6 to about 10.sup.-3, preferably from about 5.times.10.sup.-5 to about 5.times.10.sup.-4, and most preferably from about 1.5.times.10.sup.-4 to about 2.6.times.10.sup.

Abstract: Yellow dyes from substituted 2-aminothiophene and acyclic active methylene coupling components are of particular interest for dyeing polyester fibers. The dyes have the formula: ##STR1## wherein: X is a group such as alkyl, allyloxy, alkoxy, aryl or the like; Y is hydrogen, alkyl, or aryl; Z is alkyl, aryl, alkylsulfonyl, cyano or COX where X is defined above; R is cyano, carbamyl, alkanoyl, aroyl, or the like; R.sub.1 is selected from the R groups and ##STR2## wherein R.sub.2 represents the atoms necessary to complete an azole radial selected from benzothiazole, benzimidazole, benzoxazole, 1,3,4-oxadiazole, 1,3,4-thiadiazole, and pyrazole; and wherein the hydrocarbon moieties of each of the above radicals or groups may be substituted with up to three of --OH, alkoxy, hydroxyalkoxy, alkylcarbamyl, or the like.

Abstract: Thiophen-2-ylazopyrazole dyes useful for dyeing polyesters, cellulose acetate esters, and polyamides in fast yellow shades have the general formula ##STR1## wherein: X is a substituent such as alkyl, allyloxy, alkoxy, aryl, aryloxy, amino, alkylamino, arylamino, cyclohexyloxy, thienyl, cycloalkylamino, or the like; Y is hydrogen, alkyl, or aryl; Z is alkyl, aryl, alkylsulfonyl, 2-benzothiazolyl, cyano or COX; R and R.sub.1 are alkyl or aryl; R.sub.2 is hydrogen, or a substituent such as alkyl, aryl, acyl, benzothiazolyl, pyridyl, sulfolanyl, thiocarbamyl, carbamyl, alkoxycarbonyl, aroyl, or the like; wherein the hydrocarbon moieties of the above radicals may be substituted with up to three of --OH, alkoxy, hydroxyalkoxy, carbamyl, or the like; and wherein the dye molecule contains at least one SO.sub.3 M, OSO.sub.3 M, or SSO.sub.3 M water-solubilizing group.

Abstract: Disclosed are polyester blends and articles produced therefrom, wherein the blends contain copolyester material comprising one or a mixture of copolyesters such as that prepared from ethylene glycol and 1,4-cyclohexanedimethanol in certain molar proportions with terephthalic acid, blended in certain proportions with poly(ethylene isophthalate). Formed amorphous articles such as bottles, films and sheets of these blends unexpectedly are clear and show marked reduction in carbon dioxide permeability, e.g., about 20-40% lower than predicted, and have good oxygen and water vapor barrier properties. The blends are especially useful in food packaging applications such as carbonated drink bottles, where good gas and water vapor barrier properties are highly desirable.