A process for alkane chlorination comprising: (a) providing an aqueous solution comprising dissolved alkanes selected from methane, ethane or combinations thereof; (b) providing an 0.005 to 0.050 M aqueous solution of trichloroisocyanuric acid, wherein the trichloroisocyanuric acid in solution forms cyanuric acid and hypochlorous acid; and (c) contacting the aqueous solution comprising dissolved alkanes with the aqueous solution of trichloroisocyanuric acid, wherein a liquid phase reaction between the dissolved alkanes and the hypochlorous acid forms a gaseous product stream comprising at least one of chloromethane and chloroethane.

A process for alkane chlorination comprising: (a) providing an aqueous solution comprising dissolved alkanes selected from methane, ethane or combinations thereof; (b) providing an 0.005 to 0.050 M aqueous solution of trichloroisocyanuric acid, wherein the trichloroisocyanuric acid in solution forms cyanuric acid and hypochlorous acid; and (c) contacting the aqueous solution comprising dissolved alkanes with the aqueous solution of trichloroisocyanuric acid, wherein a liquid phase reaction between the dissolved alkanes and the hypochlorous acid forms a gaseous product stream comprising at least one of chloromethane and chloroethane.

The invention relates to biosourced vinylidene difluoride. The invention also relates to methods for preparation of biosourced vinylidene difluoride from various renewable raw materials. The invention also relates to homopolymers of vinylidene difluoride obtained from polymerization of said monomer, and also copolymers obtained by copolymerization of said monomer with one or several compatible comonomers. Finally, the invention relates to the use of said homopolymers or copolymers in applications, such as chemical engineering or electronics, in particular mass-market electronic devices.

The invention relates to biosourced vinylidene difluoride. The invention also relates to methods for preparation of biosourced vinylidene difluoride from various renewable raw materials. The invention also relates to homopolymers of vinylidene difluoride obtained from polymerization of said monomer, and also copolymers obtained by copolymerization of said monomer with one or several compatible comonomers. Finally, the invention relates to the use of said homopolymers or copolymers in applications, such as chemical engineering or electronics, in particular mass-market electronic devices.

The invention relates to biosourced vinylidene difluoride. The invention also relates to methods for preparation of biosourced vinylidene difluoride from various renewable raw materials. The invention also relates to homopolymers of vinylidene difluoride obtained from polymerization of said monomer, and also copolymers obtained by copolymerization of said monomer with one or several compatible comonomers. Finally, the invention relates to the use of said homopolymers or copolymers in applications, such as chemical engineering or electronics, in particular mass-market electronic devices.

A process for alkane chlorination comprising: (a) providing an aqueous solution comprising dissolved alkanes selected from methane, ethane or combinations thereof; (b) providing an 0.005 to 0.050 M aqueous solution of trichloroisocyanuric acid, wherein the trichloroisocyanuric acid in solution forms cyanuric acid and hypochlorous acid; and (c) contacting the aqueous solution comprising dissolved alkanes with the aqueous solution of trichloroisocyanuric acid, wherein a liquid phase reaction between the dissolved alkanes and the hypochlorous acid forms a gaseous product stream comprising at least one of chloromethane and chloroethane.

A process for alkane chlorination comprising: (a) providing an aqueous solution comprising dissolved alkanes selected from methane, ethane or combinations thereof; (b) providing an 0.005 to 0.050 M aqueous solution of trichloroisocyanuric acid, wherein the trichloroisocyanuric acid in solution forms cyanuric acid and hypochlorous acid; and (c) contacting the aqueous solution comprising dissolved alkanes with the aqueous solution of trichloroisocyanuric acid, wherein a liquid phase reaction between the dissolved alkanes and the hypochlorous acid forms a gaseous product stream comprising at least one of chloromethane and chloroethane.

The present application discloses a 3,3,3′,3′-tetramethyl-1,1′-spirobiindane-based phosphine ligand, an intermediate, a preparation method and uses thereof. The compound of phosphine ligand is a compound having a structure represented by formula I or formula II, or an enantiomer, a raceme, or diastereomer thereof. The phosphine ligand can be prepared via a preparation scheme in which the cheap and easily available 6,6′-dihydroxyl-3,3,3′,3′-tetramethyl-1,1′-spirobiindane is used as a raw material and the compound represented by formula III serves as the key intermediate. The new phosphine ligand developed by the present application can be used in catalytic organic reaction, in particular as a chiral phosphine ligand that is widely used in many asymmetric catalytic reactions including asymmetric hydrogenation and asymmetric allyl alkylation, and thus it has economic practicability and industrial application prospect. ##STR00001##

The present application discloses a 3,3,3′,3′-tetramethyl-1,1′-spirobiindane-based phosphine ligand, an intermediate, a preparation method and uses thereof. The compound of phosphine ligand is a compound having a structure represented by formula I or formula II, or an enantiomer, a raceme, or diastereomer thereof. The phosphine ligand can be prepared via a preparation scheme in which the cheap and easily available 6,6′-dihydroxyl-3,3,3′,3′-tetramethyl-1,1′-spirobiindane is used as a raw material and the compound represented by formula III serves as the key intermediate. The new phosphine ligand developed by the present application can be used in catalytic organic reaction, in particular as a chiral phosphine ligand that is widely used in many asymmetric catalytic reactions including asymmetric hydrogenation and asymmetric allyl alkylation, and thus it has economic practicability and industrial application prospect. ##STR00001##

The present disclosure provides a method for co-production of hydrofluorocarbons, which includes the steps of: preheating a mixture of chlorinated olefin and hydrogen fluoride; transferring the mixture to the top of a reactor; simultaneously introducing 1,1,1,2,3,3-hexafluoropropene and dichloromethane to the middle of the reactor for reaction; dividing the reactor into three to six sections; filling each section with a catalyst; obtaining reaction products at an outlet of the reactor; and separating the reaction products to obtain various hydrofluorocarbon products, respectively. The present disclosure has the advantages of a high yield, an optimal selectivity and a low energy consumption.