Liquid phase fluorination

Claim 1

A method for producing an essentially perfluorinated compound by liquid-phase fluorination, comprising: a. continuously introducing a hydrogen-containing compound into a liquid, perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium while agitating the medium so that the hydrogen-containing compound is dissolved or dispersed within the liquid medium, wherein the hydrogen containing compound is a carboxylic acid or carboxylic acid derivative; b. introducing fluorine gas diluted with an inert gas into the medium to fluorinate the hydrogen-containing compound, the fluorine being diluted so that the liquid perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium and fluorine in the vapor space do not form a flammable mixture, the amount of fluorine gas being in excess of the stoichiometric amount needed to replace all of the hydrogen atoms of the hydrogen-containing compound with fluorine; and c. continuing the fluorination until the hydrogen-containing compound is essentially perfluorinated.

Claim 2

A method for producing an essentially perfluorinated compound by liquid-phase fluorination, comprising: a. continuously introducing a hydrogen-containing compound into a liquid, perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium while agitating the medium so that the hydrogen-containing compound is dissolved or dispersed within the liquid medium, wherein the hydrogen containing compound is a carboxylic acid or carboxylic acid derivative; b. introducing fluorine gas diluted with an inert gas into the medium to fluorinate the hydrogen-containing compound, the fluorine being diluted so that the liquid perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium and fluorine in the vapor space do not form a flammable mixture, the amount of fluorine gas being in excess of the stoichiometric amount needed to replace all of the hydrogen atoms of the hydrogen-containing compound with fluorine; and c. continuing the fluorination until the hydrogen-containing compound is essentially perfluorinated.

Claim 10

A method for producing an essentially perfluorinated compound by liquid-phase fluorination, comprising: a. continuously introducing a hydrogen-containing compound into a liquid, perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium while agitating the medium so that the hydrogen-containing compound is dissolved or dispersed within the liquid medium, wherein the hydrogen-containing compound is a sulfonic acid or sulfonic acid derivative; b. introducing fluorine gas diluted with an inert gas into the medium to fluorinate the hydrogen-containing compound, the fluorine being diluted so that the liquid perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium and fluorine in the vapor space do not form a flammable mixture, the amount of fluorine gas being in excess of the stoichiometric amount needed to replace all of the hydrogen atoms of the hydrogen-containing compound with fluorine; and c. continuing the fluorination until the hydrogen-containing compound is essentially perfluorinated.

Claim 11

A method for producing an essentially perfluorinated compound by liquid-phase fluorination, comprising: a. continuously introducing a hydrogen-containing compound into a liquid, perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium while agitating the medium so that the hydrogen-containing compound is dissolved or dispersed within the liquid medium, wherein the hydrogen-containing compound is a sulfonic acid or sulfonic acid derivative; b. introducing fluorine gas diluted with an inert gas into the medium to fluorinate the hydrogen-containing compound, the fluorine being diluted so that the liquid perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium and fluorine in the vapor space do not form a flammable mixture, the amount of fluorine gas being in excess of the stoichiometric amount needed to replace all of the hydrogen atoms of the hydrogen-containing compound with fluorine; and c. continuing the fluorination until the hydrogen-containing compound is essentially perfluorinated.

Claim 13

A method for producing an essentially perfluorinated compound by liquid-phase fluorination, comprising: a. continuously introducing a hydrogen-containing compound into a liquid, perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluorether medium while agitating the medium so that the hydrogen-containing compound is dissolved or dispersed within the liquid medium, wherein the hydrogen-containing compound is a monocyclic or polycyclic aromatic compound having 6 to 30 carbon atoms; b. introducing fluorine gas diluted with an inert gas into the medium to fluorinate the hydrogen-containing compound, the fluorine being diluted so that the liquid perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium and fluorine in the vapor space do not form a flammable mixture, the amount of fluorine gas being in excess of the stoichiometric amount needed to replace all of the hydrogen atoms of the hydrogen-containing compound with fluorine; and c. continuing the fluorination until the hydrogen-containing compound is essentially perfluorinated.

Claim 14

A method for producing an essentially perfluorinated compound by liquid-phase fluorination, comprising: a. continuously introducing a hydrogen-containing compound into a liquid, perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluorether medium while agitating the medium so that the hydrogen-containing compound is dissolved or dispersed within the liquid medium, wherein the hydrogen-containing compound is a monocyclic or polycyclic aromatic compound having 6 to 30 carbon atoms; b. introducing fluorine gas diluted with an inert gas into the medium to fluorinate the hydrogen-containing compound, the fluorine being diluted so that the liquid perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium and fluorine in the vapor space do not form a flammable mixture, the amount of fluorine gas being in excess of the stoichiometric amount needed to replace all of the hydrogen atoms of the hydrogen-containing compound with fluorine; and c. continuing the fluorination until the hydrogen-containing compound is essentially perfluorinated.

Claim 15

A method for producing an essentially perfluorinated compound by liquid-phase fluorination, comprising: a. continously introducing a hydrogen-containing compound into a liquid, perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluorether medium while agitating the medium so that the hydrogen-containing compound is dissolved or dispersed within the liquid medium, wherein the hydrogen-containing compound is a hydrocarbon polymer having 10 to 10,000 carbon atoms; b. introducing fluorine gas diluted with an inert gas into the medium to fluorinate the hydrogen-containing compound, the fluorine being diluted so that the liquid perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium and fluorine in the vapor space do not form a flammable mixture, the amount of fluorine gas being in excess of the stoichiometric amount needed to replace all of the hydrogen atoms of the hydrogen-containing compound with fluorine; and c. continuing the fluorination until the hydrogen-containing compound is essentially perfluorinated.

Claim 16

A method for producing an essentially perfluorinated compound by liquid-phase fluorination, comprising: a. continously introducing a hydrogen-containing compound into a liquid, perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluorether medium while agitating the medium so that the hydrogen-containing compound is dissolved or dispersed within the liquid medium, wherein the hydrogen-containing compound is a hydrocarbon polymer having 10 to 10,000 carbon atoms; b. introducing fluorine gas diluted with an inert gas into the medium to fluorinate the hydrogen-containing compound, the fluorine being diluted so that the liquid perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium and fluorine in the vapor space do not form a flammable mixture, the amount of fluorine gas being in excess of the stoichiometric amount needed to replace all of the hydrogen atoms of the hydrogen-containing compound with fluorine; and c. continuing the fluorination until the hydrogen-containing compound is essentially perfluorinated.

Claim 17

A method for producing an essentially perfluorinated compound by liquid phase fluorination, comprising: a. providing a perfluorination reactor, wherein the reactor comprises a reaction vessel having a means for agitating a liquid contained therein; a means for introducing a hydrogen-containing compound into the reactor; means for introducing a gas into the reactor; means for removing a vaporized liquid from the reaction vessel operatively linked to a means for condensing the vaporized liquid; and a liquid return line operatively linked downstream from the condensing means wherein condensed liquid is returned to the reaction vessel; b. placing a liquid perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium in the reaction vessel; c. continuously introducing a hydrogen-containing compound into the reaction vessel while agitating the liquid medium so that the hydrogen-containing compound is dispersed within the liquid medium, wherein the hydrogen-containing compound is selected from the group consisting of a carboxylic acid, carboxylic acid derivative, sulfonic acid, sulfonic acid derivative, monocyclic or polycyclic aromatic compound having 6 to 30 carbon atoms, and hydrocarbon polymer having 10 to 10,000 carbon atoms; d. introducing fluorine gas diluted with an inert gas into the reaction vessel to fluorinate the hydrogen-containing compound, the fluorine being diluted so that the liquid perfluorobeing diluted so that the liquid perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium and fluorine in the vapor space do not form a flammable mixture, the amount of fluorine gas being in excess of the stoichiometric amount necessary to replace all of the hydrogen atoms in the hydrogen-containing compound; and e. continuing the fluorination reaction until the hydrogen-containing compound is essentially perfluorinated.

Claim 18

A method for producing an essentially perfluorinated compound by liquid phase fluorination, comprising: a. providing a perfluorination reactor, wherein the reactor comprises a reaction vessel having a means for agitating a liquid contained therein; a means for introducing a hydrogen-containing compound into the reactor; means for introducing a gas into the reactor; means for removing a vaporized liquid from the reaction vessel operatively linked to a means for condensing the vaporized liquid; and a liquid return line operatively linked downstream from the condensing means wherein condensed liquid is returned to the reaction vessel; b. placing a liquid perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium in the reaction vessel; c. continuously introducing a hydrogen-containing compound into the reaction vessel while agitating the liquid medium so that the hydrogen-containing compound is dispersed within the liquid medium, wherein the hydrogen-containing compound is selected from the group consisting of a carboxylic acid, carboxylic acid derivative, sulfonic acid, sulfonic acid derivative, monocyclic or polycyclic aromatic compound having 6 to 30 carbon atoms, and hydrocarbon polymer having 10 to 10,000 carbon atoms; d. introducing fluorine gas diluted with an inert gas into the reaction vessel to fluorinate the hydrogen-containing compound, the fluorine being diluted so that the liquid perfluorobeing diluted so that the liquid perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium and fluorine in the vapor space do not form a flammable mixture, the amount of fluorine gas being in excess of the stoichiometric amount necessary to replace all of the hydrogen atoms in the hydrogen-containing compound; and e. continuing the fluorination reaction until the hydrogen-containing compound is essentially perfluorinated.

Claim 20

A method for producing an essentially perfluorinated compound by liquid-phase fluorination, comprising: a. continuosly introducing a hydrogen-containing compound into a liquid, perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluorether medium while agitating the medium so that the hydrogen-containing compound is dissolved or dispersed within the liquid medium, wherein the hydrogen-containing compound is selected from the group consisting of a carboxylic acid, carboxylic acid derivative, sulfonic acid, sulfonic acid derivative, monocyclic or polycyclic aromatic compound having 6 to 30 carbon atoms and hydrocarbon polymer having 10 to 10,000 carbon atoms; b. introducing fluorine gas diluted with an inert gas into the medium to fluorinate the hydrogen-containing compound, the fluorine being diluted so that the liquid perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium and fluorine in the vapor space do not form a flammable mixture, the amount of fluorine gas being in excess of the stoichiometric amount necessary to replace all of the hydrogen atoms in the hydrogen-containing compound, the fluorine concentration of the gas mixture being about 10% to about 40%; c. maintaining the fluorination reaction at a temperature of from about -40° C. to about 150° C.; d. contacting the hydrogen-containing compound with a hydrogen-fluoride scavenger during the fluorination, the amount of hydrogen fluoride scavenger in relation to the hydrogen-containing compound being sufficient to react with hydrogen fluoride formed during fluorination; and e. continuing the fluorination until the hydrogen-containing compound is essentially perfluorinated.

Claim 21

A method for producing an essentially perfluorinated compound by liquid-phase fluorination, comprising: a. continuosly introducing a hydrogen-containing compound into a liquid, perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluorether medium while agitating the medium so that the hydrogen-containing compound is dissolved or dispersed within the liquid medium, wherein the hydrogen-containing compound is selected from the group consisting of a carboxylic acid, carboxylic acid derivative, sulfonic acid, sulfonic acid derivative, monocyclic or polycyclic aromatic compound having 6 to 30 carbon atoms and hydrocarbon polymer having 10 to 10,000 carbon atoms; b. introducing fluorine gas diluted with an inert gas into the medium to fluorinate the hydrogen-containing compound, the fluorine being diluted so that the liquid perfluorocarbon, perhalogenated chlorofluorocarbon or chlorofluoroether medium and fluorine in the vapor space do not form a flammable mixture, the amount of fluorine gas being in excess of the stoichiometric amount necessary to replace all of the hydrogen atoms in the hydrogen-containing compound, the fluorine concentration of the gas mixture being about 10% to about 40%; c. maintaining the fluorination reaction at a temperature of from about -40° C. to about 150° C.; d. contacting the hydrogen-containing compound with a hydrogen-fluoride scavenger during the fluorination, the amount of hydrogen fluoride scavenger in relation to the hydrogen-containing compound being sufficient to react with hydrogen fluoride formed during fluorination; and e. continuing the fluorination until the hydrogen-containing compound is essentially perfluorinated.