Abstract: Lithium metal is continuously prepared, in specially adapted electrolytic cell, by (i) continuously electrolyzing a mixture of molten salts including lithium chloride, said mixture comprising the medium of electrolysis, (ii) continuously withdrawing admixture of product lithium metal with said mixture of molten salts, and (iii) continuously discharging formed chlorine gaseous phase therefrom, wherein the medium of electrolysis is maintained at a temperature ranging from the melting point of said mixture of molten salts, at the eutectic composition thereof, to 400.degree. C., and said gaseous chlorine phase is maintained at a temperature not exceeding 300.degree. C.
Type:
Grant
Filed:
December 15, 1986
Date of Patent:
February 9, 1988
Assignee:
Rhone-Poulenc Specialites Chimiques
Inventors:
Eric Le Roux, Philippe Nataf, Serge Jacubert
Abstract: Substituted phenols are nitrated by contacting same with a 10 to 70% by weight concentrated aqueous solution of nitric acid. The subject nitration process is well adopted for the preparation, e.g., of 2,6-dichloro-4-nitrophenol, a valuable intermediate in the production of various agrochemicals/pharmaceuticals.
Abstract: An organopolysilazane composition that can be crosslinked by an energy input. The organopolysilazane composition comprises an organopolysilazane and a free radical generator in an amount effective to crosslink the organopolysilazane. The energy input capable of generating the radical may be provided in the form of heat, ultraviolet radiation, an electron beam, and the like.The crosslinked organopolysilazane compositions exhibit good thermal behavior and, in particular, can be used, after pyrolysis, as precursors of ceramic products.
Abstract: Process for the preparation of aromatic aldehydes by hydrocarbonylation of chloro- or bromoaromatic compounds. In the presence of an acceptor for an oxygen-free acid, a palladium/phosphine complex and, if appropriate, a phosphine, a mixture of carbon monoxide and hydrogen is reacted with chloro- or bromoarenetricarbonylchromiums.
Abstract: Homogeneous, flexible block copolyetheramides having a melting/softening point of at least 170.degree. C., a glass transition temperature, measured at ZHE, of at most -5.degree. C.
Abstract: Mechanically strong, H.sub.2 O-stable, macroporous spheroidal silica particulates, well adopted as catalysts/catalyst supports, are produced by (i) granulating and agglomerating a particular hydrosol of silica with a particular silica xerogel or aerogel, and (ii) drying the resultant silica particulates.
Abstract: Mixed polyester molding compositions comprising at least a pair of structurally different thermoplastic polyesters are stabilized against transesterification, whether during formulation or the downstream molding thereof, by having incorporated therein an effective amount of at least one mono-, di- or triester of orthophosphoric acid.
Abstract: A semi-permeable membrane structure that is particularly adapted for plasmapheresis includes a frame having two tubes each forming an internal conduit opening inside the frame, and a membrane on either side of the frame, each membrane being mounted with its periphery disposed on the frame. Two external rigid plates each having a suitable support for a membrane on its internal face clamp the frame and membrane between themselves. Appropriate structure is provided for keeping the two rigid plates fixed to one another and thereby maintaining the spatial relationship of the frame, membranes and plates.
Type:
Grant
Filed:
May 23, 1983
Date of Patent:
October 27, 1987
Assignee:
Rhone-Poulenc Specialites Chimiques
Inventors:
Michel Cronenberger, Paul Lateltin, Robert Rustant
Abstract: A process for preparing trifluoroacetic or trichloroacetic acid esters, wherein trifluoroacetic or trichloroacetic acid is brought together with a non-perfluorinated alcohol in liquid hydrofluoric acid and wherein the ester obtained is separated by decantation. The trifluoroacetic or trichloroacetic acid esters are used as synthesis intermediates in the pharmaceutical or the plant-protection industry.
Abstract: Novel platinum/olefin complexes, useful for the hydrosilylation curing catalysis of hardenable organopolysiloxane compositions, are facilely prepared by reacting a platinum halide with at least one alkali or alkaline earth metal carbonate or bicarbonate in the presence of an alkenylcyclohexene ligand having the general formula: ##STR1## wherein R.sub.1 is an alkenyl radical having from 2 to 6 carbon atoms, and R.sub.2 is a hydrogen atom or an inert organic radical, and said complex having a ratio, in gram-atoms of halogen to gram-atoms of platinum, ranging from virtually 0 to 4.
Abstract: Storage-stable polyisocyanurate-polyisocyanates, essentially devoid of polyisocyanate monomer and dimer over time, are conveniently prepared by catalytically cyclotrimerizing an aliphatic, cycloaliphatic or aromatic polyisocyanate in the presence of a catalytically effective amount of an aminosilyl catalyst, and terminating the cyclotrimerization reaction when predetermined desired amount of isocyanurate group has been reached, by adding to the reaction mixture a reaction terminating amount of water.
Abstract: A process for the preparation of compounds containing a difluoromethylene group in a position .alpha. to an oxygen atom. An alcohol or a phenol is brought into contact with trifluoroacetic acid or a halide or anhydride thereof in anhydrous liquid hydrofluoric acid, in the presence of boron trifluoride, in a quantity such that the absolute pressure of boron trifluoride is at least about one bar. The compounds obtained according to the invention are used as synthesis intermediates in the pharmaceutical, plant-protection, and dye industries, as anesthetics and as additives for lubricating oils.
Abstract: A process for the treatment of polyorganosilazanes and/or polyorgano(disilyl)silazanes with an effective quantity of a catalyst system comprising (i) an ionic inorganic salt of the formula M.sup.30 A.sup.-, and (II) a compound capable of complexing with the cation M.sup.+ of the salt. The M.sup.+ cation is a metal ion or a quaternary ammonium ion, and A.sup.- is a compatible anion.The polysilazanes are selected from organopolysilazanes and organopoly(disilyl)silazanes. When treated in this manner, the polysilazanes are characterized by good thermal behavior and can, in particular, be used, after pyrolysis, as precursors of ceramic products.
Abstract: Improved heat-curable organopolysiloxane compositions, easily vulcanizable into silicone elastomers, are comprised of (A) a major amount of a diorganopolysiloxane gum, (B) a reinforcing filler therefor, (C) optionally, a diorganopolysiloxane oil, (D) an organic peroxide catalyst, and minor amounts of at least three of the following four additives: (E) an organohydrogenopolysiloxane, (F) an organofluorinated polymer, (G) an organosilonxane irgabcompound bearing at least one acroyloxyalkyl or methacroyloxyalkyl substituent covalently bonded to a silicon atom thereof, and (H) a boron compound.
Abstract: A crosslinkable composition comprising at least one polysilazane containing at least 2, preferably at least 3, .tbd.SiH groups per molecule and at least 2 SiR.sub.2 groups per molecule, R.sub.2 being an unsaturated hydrocarbon radical and a catalytically effective quantity of a metal element or of a metal compound to catalyze the hydrosilylation reaction SiH/SiR.sub.2.The compositions according to the invention can crosslink under the effect of heat and can be used for coating or impregnating substrates with ceramic material after pyrolysis. The mechanical properties of the crosslinked compositions are assessed by evaluating the relative rigidity RR measured by the fiber torsion pendulum method (FIG. 1).
Abstract: The present invention relates to a process for the treatment of polysilazane in a homogeneous phase with a catalytically effective quantity of an acid catalyst selected from HClO.sub.4 and CF.sub.3 SO.sub.3 H. The polysilazane is preferably selected from the group consisting of organopolysilazane, organopoly(disilyl)silazane and mixtures thereof. The organic radicals bonded to the silicon atoms are preferably saturated or aromatic hydrocarbon radicals and the silicon atoms of the polysilazane are substantially free from any hydrogen atom bonded directly to the silicon atoms.The polysilazanes treated in this manner have good thermal behavior and, are particularly useful as precursors of ceramic products.
Abstract: Novel platinum/olefin complexes, useful for the hydrosilylation curing catalysis of hardenable organopolysiloxane compositions, are facilely prepared by reacting a platinum halide with at least one alkali or alkaline earth metal carbonate or bicarbonate in the presence of an aliphatic triene ligand having the general formula: ##STR1## wherein R.sub.1 is a linear or branched chain alkyl radical having from 1 to 6 carbon atoms, and R.sub.2 is R.sub.1 or a linear or branched chain alkenyl radical having from 2 to 16 carbon atoms and at least one site of ethylenic unsaturation, and said complex having a ratio, in gram-atoms of halogen to gram-atoms of platinum, ranging from virtually 0 to 4.
Abstract: Dimethyldichlorosilane is selectively and efficiently prepared by reacting methyl chloride with a solid contact mass comprising silicon and a catalytically effective amount of copper or a copper compound, said copper catalyst comprising (i) from about 10 to 1000 ppm of tin, antimony, or admixture thereof, or of a tin or antimony compound, or admixture thereof, (ii) from about 0.01 to 2% by weight of at least one of the metallic additives beryllium, calcium and magnesium, or compound thereof, and, optionally, (iii) from about 0.01 to 3% by weight of zinc or a zinc compound.
Abstract: Hydroquinone is selectively nascently chlorinated to monochlorohydroquinone, by reacting same with an aqueous solution of hydrochloric acid and hydrogen peroxide, in the presence of an organic solvent for, and inert to, said hydroquinone.
Abstract: Cerium and rare earth values are separated from an aqueous medium comprised thereof, by (i) anodically electrolytically treating such aqueous medium and oxidizing the Ce (III) values therein to Ce (IV) values, (ii) extracting said electrolyzed aqueous medium with a selective organic extractant for said Ce (IV) values, and permitting the extracted medium to separate into an organic phase enriched in Ce (IV) values and a product aqueous phase enriched in rare earth values, (iii) reducing the Ce (IV) values in said organic phase to Ce (III) values and admixing same with an aqueous medium, and (iv) permitting said admixture to separate into an organic phase and a product aqueous phase enriched in Ce (III) values.