Abstract: The present invention provides a catalytic cracking process. The process includes introducing at least one species of a natural or synthetic residuum containing feedstock and a catalyst into a catalytic cracker reaction zone, and thereafter cracking the feedstock into a lower molecular weight gaseous product and spent cracking catalyst with hydrocarbonaceous product deposited thereon. Among others, the lower molecular weight gaseous product includes ethylene or propylene. The spent cracking catalyst obtained from the catalytic cracker reaction zone may then be regenerated using a first and a second regeneration zone. The first regeneration zone may be operated in an oxidizing mode resulting in a remaining coke of reduced hydrogen content which lowers the moisture content of flue gas in subsequent regeneration zones.

Abstract: The present invention provides a method of producing a synthesis gas from a regeneration of a spent cracking catalyst. The method includes introducing a spent cracking catalyst into a first regeneration zone in a presence of a first atmosphere comprising a first oxygen containing gas at a first regeneration temperature. For example, a temperature that does not exceed about 1400° F., and more preferable, a temperature that ranges from about 1150° F. to about 1400° F., may be used as the first regeneration temperature. The method further includes introducing the spent cracking catalyst from the first regeneration zone into a second regeneration zone. The spent cracking catalyst is introduced into the second regeneration zone in a presence of a second atmosphere comprising a second oxygen containing gas and a carbon dioxide rich stream, and at a second regeneration temperature substantially greater than the first regeneration temperature.

Abstract: The present invention provides a catalytic cracking process. The process includes introducing at least one species of a natural or synthetic residuum containing feedstock and a catalyst into a catalytic cracker reaction zone, and thereafter cracking the feedstock into a lower molecular weight gaseous product and spent cracking catalyst with hydrocarbonaceous product deposited thereon. Among others, the lower molecular weight gaseous product includes ethylene or propylene. The spent cracking catalyst obtained from the catalytic cracker reaction zone may then be regenerated using a first and a second regeneration zone. The first regeneration zone may be operated in an oxidizing mode resulting in a remaining coke of reduced hydrogen content which lowers the moisture content of flue gas in subsequent regeneration zones.

Abstract: The present invention provides a method of producing a synthesis gas from a regeneration of a spent cracking catalyst. The method includes introducing a spent cracking catalyst into a first regeneration zone in a presence of a first atmosphere comprising a first oxygen containing gas at a first regeneration temperature. For example, a temperature that does not exceed about 1400° F., and more preferable, a temperature that ranges from about 1150° F. to about 1400° F., may be used as the first regeneration temperature. The method further includes introducing the spent cracking catalyst from the first regeneration zone into a second regeneration zone. The spent cracking catalyst is introduced into the second regeneration zone in a presence of a second atmosphere comprising a second oxygen containing gas and a carbon dioxide rich stream, and at a second regeneration temperature substantially greater than the first regeneration temperature.

Abstract: The present invention provides a method of producing a synthesis gas from a regeneration of spent cracking catalyst. The method includes introducing a spent cracking catalyst into a first regeneration zone in a presence of a first oxygen and carbon dioxide atmosphere and at a first regeneration temperature. For example, a temperature that does not exceed about 1400° F., and more preferable a temperature that ranges from about 1150° F. to about 1400° F., may be used as the first regeneration temperature. The method further includes introducing the spent cracking catalyst from the first regeneration zone into a second regeneration zone in a presence of a second oxygen and carbon dioxide atmosphere, and producing a synthesis gas from cracking deposits located on the spent cracking catalyst within the second regeneration zone at a second regeneration temperature substantially greater than said first regeneration temperature.

Abstract: The present invention provides a method of producing a synthesis gas from a regeneration of spent cracking catalyst. The method includes introducing a spent cracking catalyst into a first regeneration zone in a presence of a first oxygen and carbon dioxide atmosphere and at a first regeneration temperature. For example, a temperature that does not exceed about 1400° F., and more preferable a temperature that ranges from about 1150° F. to about 1400° F., may be used as the first regeneration temperature. The method further includes introducing the spent cracking catalyst from the first regeneration zone into a second regeneration zone in a presence of a second oxygen and carbon dioxide atmosphere, and producing a synthesis gas from cracking deposits located on the spent cracking catalyst within the second regeneration zone at a second regeneration temperature substantially greater than said first regeneration temperature.

Abstract: Method and apparatus for controlling the flow of a molten mass reaction medium into a reaction zone, said method comprising introducing the molten mass medium and a control gas into an elongated, vertical supply conduit leading to the reaction zone whereby the control gas exerts a gas-lift effect on the molten medium and apportioning the flow of control gas to the desired flow of molten medium; said apparatus comprising a reaction zone, supply conduit means for supplying a molten mass reaction medium to said reaction zone, and means for controllably introducing a control gas into said supply conduit means for regulating the flow of said molten mass reaction medium therethrough.

Abstract: A process and apparatus for regenerating fluidizable particulate cracking catalysts wherein a mixture of spent catalyst particles contaminated with carbonaceous deposits from a catalytic cracker and sufficient hot regenerated catalyst particles to bring the temperature of the mixture to the minimum temperature at which rapid oxidation of the carbonaceous deposits will be induced, are entrained in a high velocity gas stream containing sufficient oxygen to oxidize substantially all of the carbonaceous deposits on the spent catalyst particles to carbon dioxide and carbon monoxide and the resulting dilute phase catalyst particle stream is passed upwardly through a primary regeneration zone wherein the carbonaceous deposits are oxidized and the catalyst particles regenerated to a carbon content of less than 0.

Abstract: Disclosed is a process for hydrotreating hydrocarbon feedstocks and for recovering from the resulting effluent stream selected hydrocarbon fractions, and hydrogen for recycle and other uses with improved purity. Relatively pure hydrogen is provided by separating the effluent stream into a hydrogen-containing gaseous stream and a liquid phase hydrocarbon product, and then contacting the gaseous hydrogen-containing stream in a first absorption step with the liquid phase hydrocarbon product obtained in the gas-liquid separation step, and in a second extraction step with a stabilized portion of the liquid phase hydrocarbon product.

Abstract: High-purity C.sub.7 and/or C.sub.8 aromatic hydrocarbons are produced by reforming a C.sub.7 or C.sub.8 full boiling carbon number naphtha feed fraction or combinations thereof under reforming conditions of sufficient severity to convert essentially all of the non-aromatic portion of the naphtha feed boiling in the C.sub.7 to C.sub.8 aromatic boiling range to C.sub.7 and/or C.sub.8 aromatics, and then separating the reformate by fractional distillation into high-purity fractions of C.sub.7 and/or C.sub.8 aromatic hydrocarbons. Preferably, the C.sub.7 and/or C.sub.8 full boiling carbon number naphtha feed fraction is reformed in a plurality of reformer reaction stages with increasingly more severe conditions in order to maximize the yield of the C.sub.7 and C.sub.8 aromatics.

Abstract: Disclosed is a process for the production of highly aromatic reformates in high yield from a naphtha feed fraction by high-severity catalytic reforming using a reforming catalyst which includes a hydrocracking promotor metal. The process comprises reforming the stock under conditions of high severity in a plurality of sequentially arranged reaction zones in which the concentration of the hydrocracking promotor metal of the reforming catalyst is adjusted to provide a minimal hydrocracking activity relative to the other reforming reactions to the catalyst in the first reaction zones, and an enhanced hydrocracking activity to the catalyst in the last reaction zones. The reformates produced according to this process are particularly useful in the blending of high aromatic content gasoline and/or in the production of high purity aromatic hydrocarbons.

Abstract: Disclosed is a process for the production of highly aromatic reformates, having a minimum of nonaromatic material, in high yield from a naphtha feed fraction by high-severity catalytic reforming, using a halogen-promoted reforming catalyst. The process comprises reforming the naphtha feed under reforming conditions of high severity in a plurality of sequentially arranged reaction zones in which the concentration of the halogen component of the reforming catalyst is adjusted to provide a minimal hydrocracking activity relative to the other reforming reactions to the catalyst in the first reaction zones, and an enhanced hydrocracking activity to the catalyst in the last reaction zones. The reformates produced according to this process are particularly useful in the blending of high aromatic content gasolines and/or in the production of high purity aromatic hydrocarbons.