Abstract: There are provided methods of treating a catalyst-containing reactor system with a liquid solvent to remove contaminants from the reactor system. An exemplary method includes the steps of: isolating the reactor system to be treated from upstream and downstream equipment; reducing the temperature and pressure of the isolated reactor system by flushing with a hydrogen rich gas; injecting a non-aqueous liquid solvent into the reactor system at an injection point while continuously flowing hydrogen-rich gas through the reactor system; maintaining the solvent in a liquid state while flowing the solvent continuously through the reactor system; and terminating the step of injecting solvent and terminating the continuous flowing of hydrogen-rich gas. The exemplary method is free of the injecting of a carrier gas into the reactor system comprising alkanes selected from the methane, ethane, propane, butane and pentane.

Abstract: A method for preparing a ruthenium catalyst, including a step of reducing a ruthenium catalyst precursor by holding the ruthenium catalyst precursor in an aqueous solution containing a metal salt at a temperature within the range of more than 180° C. and 220° C. or less and a hydrogen partial pressure within the range of 0.6 MPa or more and 5 MPa or less. A method for producing a cycloolefin, including a step of preparing a ruthenium catalyst by the method including a step of reducing a ruthenium catalyst precursor in an aqueous solution containing a metal salt by holding the ruthenium catalyst precursor at a temperature within the range of more than 180° C. and 220° C. or less and a hydrogen partial pressure within the range of 0.6 MPa or more and 5 MPa or less, and a step of partially hydrogenating a monocyclic aromatic hydrocarbon by use of the ruthenium catalyst obtained.

Abstract: The present invention relates to a method for preparing a synthetic fuel on a vessel above a stranded gas field or an oil & gas field by a GTL-FPSO process, more particularly to a method for preparing a synthetic fuel with superior economic feasibility, productivity and efficiency using a compact GTL (gas to liquid) apparatus that can be used for a stranded gas field or an oil & gas field and an FPSO (floating production, storage and offloading) process under a condition optimized for the ratio of carbon dioxide in the stranded gas field or the oil & gas field and an apparatus for the same.

Abstract: A process for separating xylene from a feedstock in which the feedstock is separated into a xylene stream, a benzene rich stream and a light ends stream. Two separation zones may be utilized in which liquid from both is sent to a stabilization zone and the vapor from the stabilization zone is combined with a stream prior to the stream entering the second separation zone.

Abstract: A process is presented for the management of sulfur on a catalyst. The catalyst is a dehydrogenation catalyst, and sulfur accumulates during the dehydrogenation process. Sulfur compounds are stripped from the spent catalyst and the catalyst is cooled before the regeneration process. The process includes controlling the amount of sulfur that needs to be removed from the catalyst before regeneration.

Abstract: This invention relates to the field of Fischer-Tropsch catalysis, in particular to activation of a Fischer-Tropsch catalyst. More particularly the invention relates to a method of activating an iron based Fischer-Tropsch catalyst which includes iron in a positive oxidation state by contacting in a reactor said iron based catalyst with a reducing gas selected from the group consisting of CO and a combination of H2 and CO; at a temperature of at least 245° C. and below 280° C.; at a reducing gas pressure of above 0.5 MPa and not more than 2.2 MPa; and at a GHSV of total gas fed to the reactor of at least 6000 ml(N)/g cat/h, thereby reducing the iron that is in a positive oxidation step in the catalyst.

Abstract: A process for regenerating a fixed bed of Fischer-Tropsch catalyst particles, of which at least 40 wt % of the catalyst particles have a size of at least 1 mm, in situ in a Fischer-Tropsch reactor tube. The process comprises the steps of: (i) optionally oxidizing the catalyst at a temperature between 200 and 400° C.; (ii) oxidizing the catalyst at a temperature above 580° C. and below 670° C.; and (iii) reducing the catalyst with hydrogen or a hydrogen comprising gas. This process may be preceded by a step in which Fischer-Tropsch product is removed from the catalyst.

Abstract: The present invention provides a process for hydrocarbon conversion, especially for producing aromatic hydrocarbons, which comprises: (a) alternately contacting a hydrocarbon feed, especially a lower alkane feed, with a hydrocarbon conversion catalyst, especially an aromatization catalyst, under hydrocarbon conversion, especially aromatization reaction conditions, in a reactor for a short period of time, preferably 30 minutes or less, to produce reaction products and then contacting the catalyst with hydrogen-containing gas at elevated temperature for a short period of time, preferably 10 minutes or less, (b) repeating the cycle of step (a) at least one time, (c) regenerating the catalyst by contacting it with an oxygen-containing gas at elevated temperature and (d) repeating steps (a) through (c) at least one time.

Abstract: A process is disclosed for separation and recovery of vanadium, molybdenum, iron, tungsten, cobalt and nickel from alumina-based materials, mattes, ores, manufacturing by-products and waste. These elements are oxidized. The oxides are reacted with gaseous HCl to form volatile chloride-bearing compounds that subsequently sublimate. The volatile compounds are condensed in a downward-stepped thermal gradient that allows collection of moderate to high purity compounds of individual elements with exception of a nickel-cobalt co-condensate. Nickel is separated from cobalt by precipitation of nickel chloride from concentrated HCl pressurized with gaseous HCl.

Abstract: A combination of moving bed regeneration technology and CO oxidation technology is used in a novel moving bed regeneration apparatus containing an integral CO oxidation zone to solve the problem of regenerating a coke-containing catalyst that does not contain a CO oxidation promoter without generating an effluent flue gas stream containing hazardous and undesired amounts of CO. The CO oxidation zone is located in the flue gas collection zone within the moving bed regeneration apparatus and functions autogenously to eliminate the CO hazard by oxidizing CO to CO2 with a portion of the unreacted oxygen withdrawn from the coke combustion zone of the moving bed regeneration apparatus.

Abstract: Disclosed is a process for combusting dry gas to heat the air supplied to an FCC regenerator to increase its temperature and minimize production of undesirable combustion products. Preferably, the dry gas is a selected FCC product gas. Alternatively or additionally, dry gas from an FCC product stream is separated and delivered to an expander to recover power before combustion.

Abstract: A process is disclosed for separation and recovery of vanadium, molybdenum, iron, tungsten, cobalt and nickel from alumina-based materials, mattes, ores, manufacturing by-products and waste. These elements are oxidized. The oxides are reacted with gaseous HCl to form volatile chloride-bearing compounds that subsequently sublimate. The volatile compounds are condensed in a downward-stepped thermal gradient that allows collection of moderate to high purity compounds of individual elements with exception of a nickel-cobalt co-condensate. Nickel is separated from cobalt by precipitation of nickel chloride from concentrated HCl pressurized with gaseous HCl.

Abstract: A process for regenerating a fixed bed of Fischer-Tropsch catalyst particles, of which at least 40 wt % of the catalyst particles have a size of at least 1 mm, in situ in a Fischer-Tropsch reactor tube. The process comprises the steps of: (i) optionally oxidising the catalyst at a temperature between 200 and 400° C.; (ii) oxidising the catalyst at a temperature above 580° C. and below 670° C.; and (iii) reducing the catalyst with hydrogen or a hydrogen comprising gas. This process may be preceded by a step in which Fischer-Tropsch product is removed from the catalyst.

Abstract: A catalyst for purification of exhaust gas in which a noble metal is supported on a metal-oxide support wherein, in a oxidation atmosphere, the noble metal exists on the surface of the support in high oxidation state, and the noble metal binds with a cation of the support via an oxygen atom on the surface of the support to form a surface oxide layer and, in a reduction atmosphere, the noble metal exists on the surface of the support in a metal state, and an amount of noble metal exposed at the surface of the support, measured by CO chemisorption, is 10% or more in atomic ratio to a whole amount of the noble metal supported on the support.

Abstract: A process is disclosed for separation and recovery of vanadium, molybdenum, iron, tungsten, cobalt and nickel from alumina-based materials, mattes, ores, manufacturing by-products and waste. These elements are oxidized. The oxides are reacted with gaseous HCl to form volatile chloride-bearing compounds that subsequently sublimate. The volatile compounds are condensed in a downward-stepped thermal gradient that allows collection of moderate to high purity compounds of individual elements with exception of a nickel-cobalt co-condensate. Nickel is separated from cobalt by precipitation of nickel chloride from concentrated HCl pressurized with gaseous HCl.

Abstract: A catalyst for the production of methacrylic acid comprising a heteropolyacid compound containing phosphorus and molybdenum is regenerated by a method comprising the steps of drying a mixture containing a deactivated catalyst, an ammonium ion, a nitrate ion and water, molding the dried mixture, firstly calcining the molded product in an atmosphere of an oxidizing gas at a temperature of 360 to 410° C., and then secondly calcining the product in an atmosphere of a non-oxidizing gas at a temperature of 420 to 500° C. The regenerated catalyst has substantially the same catalytic activity as a fresh catalyst in a gas phase catalytic oxidation reaction of methacrolein, isobutylaldehyde, isobutane or isobutyric acid to prepare methacrylic acid.

Abstract: A process for regeneration of a catalyst that comprises at least one EUO-structural-type zeolite in acid form and at least one hydro-dehydrogenating metal, used in a process for isomerization of a hydrocarbon feedstock that comprises aromatic compounds with eight carbon atoms, comprising at least a) a stage for eliminating a majority of the coke, deposited on said catalyst, by combustion in the presence of a gas that contains oxygen at a temperature that is less than or equal to 600° C., and b) a stage for oxychlorination of the product that is obtained from stage a), carried out between 200 and 550° C. in the presence of at least one gas mixture that contains at least oxygen, water and chlorine and/or at least one chlorinated compound, is described.

Abstract: A process in which halogen is recovered from a cyclic operation for regenerating hydrocarbon conversion catalysts is disclosed. The process uses an arrangement of beds of adsorbent and a circulating stream to return the halogen-containing materials to a regeneration circuit.

Abstract: A process for continuously regenerating catalyst particles comprising: passing deactivated catalyst particles downwards in sequence through the first coke-burning zone, second coke-burning zone, oxychlorination zone, and calcination zone in the regenerator, wherein the catalyst particles are contacted with the regeneration gas from the second coke-burning zone, the supplemented dry air, and an inert gas in the first coke-burning zone; introducing an oxygen-containing regeneration gas from the second coke-burning zone into the regenerator, wherein said gas is contacted with the catalyst particles from the first coke burning zone; withdrawing the regeneration gas from the regenerator through the first coke-burning zone and, after the recovery system, recycling it to the second coke-burning zone. The regeneration gas may pass the catalyst bed in either a centrifugal or centripetal way.

Abstract: The invention relates to a process for converting an oxygenate feedstock into an olefin product stream comprising (a) contacting an oxygenate feedstock with a molecular sieve catalyst in a reactor under conditions effective to convert the feedstock into an olefin product stream and to form carbonaceous deposits on the catalyst; (b) contacting at least a portion of the catalyst having said carbonaceous deposits with an oxygen containing gas under conditions effective to obtain a regenerated catalyst having a reduced carbonaceous deposit level and having an increased molecular oxygen content; (c) removing at least 60% by volume of said molecular oxygen from the regenerated catalyst based upon the total volume of molecular oxygen; (d) returning said regenerated catalyst to said reactor; and (e) repeating steps (a)–(d).

Abstract: A process for regenerating a dehydrogenation catalyst comprises the steps (a)-(f): (a) flushing with inert gas at a pressure of from 0.5 to 2.0 bar and a gas hourly velocity of from 1000 to 50 000 h?1; (b) passing an oxygen-containing gas mixture comprising an inert gas through the catalyst at a pressure of from 2 to 20 bar and a gas hourly velocity of from 1000 to 50 000 h?1 for from 0.25 to 24 hours while increasing the oxygen concentration stepwise or continuously from an initial value of from 0.01 to 1% by volume of O2 to a final value of from 10 to 25% by volume of O2; (c) optionally passing an oxygen-containing gas mixture comprising an inert gas through the catalyst at a pressure of from 0.5 to 20 bar and a gas hourly velocity of from 10 to 500 h?1 for from 0.25 to 100 h, with the oxygen concentration being from 10 to 25% by volume of O2; (d) optionally changing the pressure repeatedly, rapidly and in opposite directions by a factor of from 2 to 20 within the range from 0.

Abstract: A method of recovering halogen-containing materials from the cyclic catalyst regeneration operation of a catalytic hydrocarbon conversion process is disclosed. The method uses an arrangement of beds of adsorbent to return the halogen-containing materials to a circulating regeneration circuit.

Abstract: A method of recovering halogen-containing materials from the cyclic catalyst regeneration operation of a catalytic hydrocarbon conversion process is disclosed. The method uses an arrangement of beds of adsorbent to maintain the halogen-containing materials within a circulating regeneration circuit.

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: Provided is a process for preparing a non-pyrophoric catalyst having about 2 to 20 wt. % of a copper component, wherein at least 50 wt. % of the copper component is in the form of a copper oxide, aluminum oxide-spinel. The catalyst can be prepared by forming a mixture of a copper precursor and an alumina precursor, coextruding the mixture, drying the coextrudate and calcining the dried coextrudate at a temperature of at least 600° C. In other aspects, the invention also relates to processes for the activation of copper-based catalysts and for the regeneration of deactivated copper-based catalysts.

Abstract: A process for regenerating a dehydrogenation catalyst comprises the steps (a)-(f):

Abstract: A deactivated sorbent composition is reactivated by contacting the deactivated sorbent with a reducing stream under activation conditions sufficient to reduce the amount of sulfates associated with the sorbent composition.

Abstract: Catalyst activation of a platinum reforming catalyst system contained in a multiple reactor system by simultaneously reducing the catalyst with hydrogen while introducing a nonmetallic chlorine-containing compound into a reactor of the multiple reactor system in an amount to add from about 0.05 to about 0.3 weight percent chlorine to the catalyst and thereafter purging the system with about 100 to about 50,000 cubic feet of hydrogen per cubic foot of catalyst resulting in a reforming system having increased activity and providing enhanced RON values with reduced cracking of feedstock.

Abstract: A process for continuously regenerating catalyst particles comprising: passing deactivated catalyst particles downwards in sequence through the first coke-burning zone, second coke-burning zone, oxychlorination zone, and calcination zone in the regenerator, wherein the catalyst particles are contacted with the regeneration gas from the second coke-burning zone, the supplemented dry air, and an inert gas in the first coke-burning zone; introducing an oxygen-containing regeneration gas from the second coke-burning zone into the regenerator, wherein said gas is contacted with the catalyst particles from the first coke burning zone; withdrawing the regeneration gas from the regenerator through the first coke-burning zone and, after the recovery system, recycling it to the second coke-burning zone. The regeneration gas may pass the catalyst bed in either a centrifugal or centripetal way.

Abstract: A process for the desulfurization, and reactivation of a sulfur deactivated catalyst constituted of cobalt composited with a titania support. The sulfur deactivated cobalt titania catalyst is first contacted with a gaseous stream of molecular oxygen at temperature sufficiently high to oxidize the sulfur component of the catalyst. The sulfur oxidized catalyst is next contacted with a liquid, preferably water, to remove the oxide, or oxides of the sulfur. The catalyst is then contacted with a reducing agent, suitably hydrogen, to restore the activity of the catalyst. During the treatment there is no substantial loss, if any, of cobalt from the catalyst.

Abstract: Process for regeneration of a catalytic moving bed in which the catalyst successively passes through at least one combustion zone A, at least one halogenation zone B, and at least one calcination zone C, whereby this process operates in a partial-regeneration-mode, the partially coked catalyst that is obtained from the last combustion zone passes into the halogenation zone in which the amount of halogen and the amount of oxygen are essentially zero--the valves of tubes (19) and (20) are then virtually closed--and the catalyst then passes through the calcination zone in which the amount of oxygen is essentially zero--the valve of tube (11) is then virtually closed.

Abstract: The present invention is directed toward improved processes for the regeneration of noble metal-containing catalysts wherein iron contamination of the catalyst during regeneration is significantly diminished. It has been found that maintenance of any iron present in contact with the catalyst in the oxidized state (e.g., as Fe.sub.2 O.sub.3 or Fe.sub.3 O.sub.4) during contact of the catalyst with a source of halogen in the regeneration haliding step results in a marked decrease in the degree of catalyst contamination by iron species.

Abstract: A process for decreasing the air-sensitivity of a carbon monoxide oxidation catalyst composition is provided. The process can comprise, consist essentially of, or consist of (1) heating the composition at a temperature sufficient to produce an activated composition; (2) contacting the activated composition with an oxygen-containing fluid whereby a deactivated composition is produced; and (3) contacting the deactivated composition under reducing atmosphere and at a low temperature wherein the composition can comprise, consist essentially of, or consist of platinum, iron, and an inorganic support; or can comprise, consist essentially of, or consist of palladium, platinum, iron, and an inorganic support.

Abstract: A method for recovering the activity of a ruthenium catalyst which comprises a step of bringing a ruthenium catalyst decreased in activity by its use in hydrogenation of an unsaturated organic compound into contact with oxygen in a liquid phase, and a step of maintaining the catalyst at a hydrogen partial pressure lower than that at the hydrogenation and a temperature not lower than a temperature lower by 50.degree. C. than the hydrogenation temperature.

Abstract: The present invention is directed toward improved processes for the regeneration of noble metal-containing catalysts wherein iron contamination of the catalyst during regeneration is significantly diminished. It has been found that maintenance of any iron present in contact with the catalyst in the oxidized state (e.g., as Fe.sub.2 O.sub.3 or Fe.sub.3 O.sub.4) during contact of the catalyst with a source of halogen in the regeneration haliding step results in a marked decrease in the degree of catalyst contamination by iron species.

Abstract: A method is disclosed for recovering chlorine-containing species from the outlet gas of a hydrocarbon conversion process with a cyclic regeneration operation. The outlet gas from an off-stream catalyst bed in which regeneration is occurring is passed to another off-stream catalyst bed which contains spent catalyst and which is maintained at sorption conditions. The spent catalyst particles sorb the chlorine-containing species from the outlet gas. This method captures and retains within the hydrocarbon conversion process chlorine-containing species that would otherwise be scrubbed and lost from the process and that would need to be replaced by the injection of make-up chlorine-containing species. This method results in significant savings in operating costs of a cyclic regeneration process. This method is adaptable to many processes for the catalytic conversion of hydrocarbons in which deactivated catalyst are regenerated by a cyclic regeneration operation.

Abstract: The invention concerns a process for the regeneration of a used hydrocarbon treatment catalyst, preferably a reforming catalyst, containing at least one precious metal preferably platinum, optionally at least one additional metal selected from the group formed by metals from groups 7, 8, 9, 10, 13 and 14 of the periodic classification of the elements and copper, optionally and preferably at least one halogen, preferably chlorine, and at least one porous support, preferably alumina, said process comprising at least one of the following two successive steps: at least one step (1) for the combustion of the coke present on said catalyst, carried out in the presence of an oxygen-containing gas, at a temperature in the range of 300.degree. C. to 680.degree. C. for a time in the range 0.3 to 7 hours, at least one step (2) for oxyhalogenation, preferably oxychlorination, carried out in a controlled air atmosphere, at a temperature in the range 350.degree. C. to 550.degree. C., for a time in the range 0.

Abstract: A cobalt catalyst for use in the Fischer Tropsch reaction of synthesis gas to form hydrocarbons is activated or regenerated by treatment of a cobalt containing catalyst with a gas containing carbon monoxide, said gas containing less than 30% v hydrogen. The catalyst obtained has increased activity and greater selectivity towards producing C.sub.5 + hydrocarbons.

Abstract: Macrocyclic polyester oligomers are converted to linear polyesters by contact at a temperature of about 160.degree.-300.degree. C. with a cyclic titanium catalyst such as di-(1-butyl)-2,2-dimethylpropane-1,3-dioxytitanate, bis(2,2-dimethyl-1,3-propylene) titanate or 1-(1-butoxy)-4-methyl-2,6,7-trioxa-1-titanabicyclo[2.2.2]octane. Such catalysts have high activity and produce linear or branched polyesters of very high molecular weight.

Abstract: A cobalt catalyst for use in the Fischer Tropsch reaction of synthesis gas to form hydrocarbons is activated or regenerated by treatment of a cobalt containing catalyst with a gas containing carbon monoxide, said gas containing less than 30% v hydrogen. The catalyst obtained has increased activity and greater selectivity towards producing C.sub.5+ hydrocarbons.

Abstract: There is provided a process for regenerating a coked catalyst comprising a zeolite and a noble metal such as platinum. The process involves treating the coked catalyst under somewhat mild oxidation conditions, whereby a sufficient portion of the coke is removed from the catalyst to restore the hydrocarbon sorption properties of the zeolite component to the level observed in the non-coked form. Surprisingly, the original activity of the catalyst is substantially restored, even though a substantial amount of coke remains on the regenerated catalyst.

Abstract: Disclosed is a method for starting up a cyclic or semi-cyclic reforming reactor after catalyst regeneration. The method mitigates disruptions to the reforming unit after catalyst regeneration, such as excessive light gas make and a decrease in recycle hydrogen purity.

Abstract: A method for regenerating a Group VIII noble metal catalyst which has been contaminated with coke during a reforming process. The method comprises (a) burning off the coke from the catalyst, redispersing the noble metal on the surface of the catalyst support by contacting the catalyst with halogen gas and carbon dioxide, and (c) chemically reducing the catalyst. The presence of carbon dioxide in the redispersing step improves the activity of the regenerated catalyst.

Abstract: A method for countering the adverse effect of contaminating metals on a crystalline aluminosilicate catalyst comprising contacting the catalyst with a reducing gas under suitable conditions. In a preferred embodiment, the catalyst contains antimony.

Abstract: A method for regenerating a Group VIII noble metal catalyst which has been contaminated with coke during a reforming process. The method comprises (a) burning off the coke from the catalyst, (b) redispersing the noble metal on the surface of the catalyst support by contacting the catalyst with halogen gas and carbon dioxide, and (c) chemically reducing the catalyst. The presence of carbon dioxide in the redispersing step improves the activity of the regenerated catalyst.

Abstract: The useful life of the palladium dehydrogenation catalyst used in the preparation of 2-alkylpyrimidines from 1,3-diaminopropane and an appropriate alkanecarboxylic acid in a continuous vapor phase process is substantially increased by employing a stoichiometric excess of the carboxylic acid and by using catalyst pellets of less than 3-4 mm diameters. Additionally, the dehydrogenation catalyst can be regenerated in situ by controlled air oxidation below 350.degree. C.

Abstract: A process for regenerating a coke contaminated reforming catalyst comprising platinum on a molecular sieve, said process consisting essentially of contacting said catalyst with a halogen-free oxygen-containing gas at a temperature of less than 780.degree. F. for a sufficient period of time such that the aromatization activity is restored to within 20.degree. F. of the activity said catalyst possessed at the start of the previous run cycle.

Abstract: A method for countering the adverse effect of contaminating metals on a crystalline aluminosilicate catalyst comprising contacting the catalyst with a reducing gas under suitable conditions.In a preferred embodiment, the catalyst contains antimony.

Abstract: A method for countering the adverse effect of contaminating metals on a cystalline aluminosilicate catalyst comprising contacting the catalyst with a metallic passivating agent to effect some passivation of the effects of the contaminant metals and with a reducing gas under suitable conditions. In a preferred embodiment, the catalyst contains antimony.