Catalytic Distillation Technologies, Chemical Research & Licensing Company, aTexas corporation and Lummus Technology LLC, a Delaware limited liability compa ny ()
45 - Services juridiques; services de sécurité; services personnels pour individus
Produits et services
Licensing of oil refining and petrochemical technologies; consultation services in the field of the licensing of oil refining and petrochemical technology
2.
Selective hydrodesulfurization of FCC gasoline to below 10 ppm sulfur
A process for reducing the sulfur content of a hydrocarbon stream is disclosed. A full range cracked naphtha is contacted with a hydrogenation catalyst to convert at least a portion of the dienes and mercaptans to thioethers and to hydrogenate at least a portion of the dienes. The full range cracked naphtha is fractionated into a light naphtha fraction, a medium naphtha fraction, and a heavy naphtha fraction. The heavy naphtha fraction is hydrodesulfurized. The medium naphtha fraction is mixed with hydrogen and gas oil to form a mixture, which is contacted with a hydrodesulfurization catalyst to produce a medium naphtha fraction having a reduced sulfur concentration. The light, heavy, and medium naphtha fractions may then be recombined to form a hydrodesulfurized product having a sulfur content of less than 10 ppm in some embodiments.
C10G 65/06 - Traitement des huiles d'hydrocarbures, uniquement par plusieurs procédés d'hydrotraitement uniquement par plusieurs étapes en série ne comprenant que des étapes de raffinage au moins une étape étant une hydrogénation sélective des dioléfines
B01D 3/00 - Distillation ou procédés d'échange apparentés dans lesquels des liquides sont en contact avec des milieux gazeux, p. ex. extraction
B01J 8/04 - Procédés chimiques ou physiques en général, conduits en présence de fluides et de particules solidesAppareillage pour de tels procédés avec des particules immobiles, p. ex. dans des lits fixes le fluide passant successivement à travers plusieurs lits
C10G 45/02 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage
C10G 45/32 - Hydrogénation sélective des composés dioléfiniques ou acétyléniques
C10G 65/00 - Traitement des huiles d'hydrocarbures, uniquement par plusieurs procédés d'hydrotraitement
C10G 65/16 - Traitement des huiles d'hydrocarbures, uniquement par plusieurs procédés d'hydrotraitement uniquement par plusieurs étapes en parallèle ne comprenant que des étapes de raffinage
A process and apparatus for improving the production of coke having a high volatile combustible material content are disclosed. The process may include, for example: heating a coker feedstock to a coking temperature to produce a heated coker feedstock; contacting the heated coker feedstock with a quench medium to reduce a temperature of the heated coker feedstock and produce a quenched feedstock; feeding the quenched feedstock to a coking drum; subjecting the quenched feedstock to thermal cracking in the coking drum to (a) crack a portion of the quenched feedstock to produce a cracked vapor product, and (b) produce a coke product having a volatile combustible material (VCM) concentration in the range from about 13% to about 50% by weight, as measured by ASTM D3175.
C10B 41/08 - Dispositifs de sécurité, p. ex. dispositifs de signalisation ou de commande utilisés lors du défournement pour la sortie des gaz de distillation
C10B 27/06 - Parties constitutives des conduites, p. ex. valves
C10G 9/00 - Craquage thermique non catalytique, en l'absence d'hydrogène, des huiles d'hydrocarbures
C10B 41/00 - Dispositifs de sécurité, p. ex. dispositifs de signalisation ou de commande utilisés lors du défournement
C10B 55/00 - Cokéfaction des huiles minérales, bitumes, goudrons ou analogues, ou de leurs mélanges, avec des matières carbonées solides
C10B 57/04 - Autres procédés de carbonisation ou de cokéfactionCaractéristiques générales des procédés de distillation destructive utilisant des charges de composition spéciale
A process for the production of olefins from at least one of an alcohol and ether, the process including: contacting at least one alcohol or ether with a hydrofluoric acid-treated amorphous synthetic alumina-silica catalyst under decomposition conditions to produce an olefin. Also disclosed is a process for the production of isobutylene from methyl tertiary butyl ether, the process including: feeding methyl tertiary butyl ether (MTBE) to a reactor having at least one reaction zone containing a hydrofluoric acid-treated amorphous synthetic alumina-silica catalyst; contacting the MTBE with the hydrofluoric acid-treated amorphous synthetic alumina-silica catalyst under decomposition conditions to produce a reactor effluent comprising isobutylene, unreacted MTBE, heavies, and methanol; feeding the reactor effluent to a first distillation column; separating the isobutylene from the unreacted MTBE, heavies, and the methanol in the first distillation column to recover a first bottoms fraction comprising heavies, unreacted MTBE, and methanol and an isobutylene-rich overheads fraction.
C07C 1/20 - Préparation d'hydrocarbures à partir d'un ou plusieurs composés, aucun d'eux n'étant un hydrocarbure à partir de composés organiques ne renfermant que des atomes d'oxygène en tant qu'hétéro-atomes
B01J 38/54 - Traitement par un liquide ou traitement en phase liquide, p. ex. en solution ou en suspension avec des liquides organiques contenant des halogènes
B01J 38/64 - Traitement par un liquide ou traitement en phase liquide, p. ex. en solution ou en suspension avec une substance alcalineTraitement par un liquide ou traitement en phase liquide, p. ex. en solution ou en suspension avec des sels
B01J 38/60 - Traitement par un liquide ou traitement en phase liquide, p. ex. en solution ou en suspension avec des acides
B01J 38/66 - Traitement par un liquide ou traitement en phase liquide, p. ex. en solution ou en suspension avec une substance alcalineTraitement par un liquide ou traitement en phase liquide, p. ex. en solution ou en suspension avec des sels avec de l'ammoniac ou ses composés
A process for reducing the sulfur content of a hydrocarbon stream is disclosed. A full range cracked naphtha is contacted with a hydrogenation catalyst to convert at least a portion of the dienes and mercaptans to thioethers and to hydrogenate at least a portion of the dienes. The full range cracked naphtha is fractionated into a light naphtha fraction, a medium naphtha fraction, and a heavy naphtha fraction. The heavy naphtha fraction is hydrodesulfurized. The medium naphtha fraction is mixed with hydrogen and gas oil to form a mixture, which is contacted with a hydrodesulfurization catalyst to produce a medium naphtha fraction having a reduced sulfur concentration. The light, heavy, and medium naphtha fractions may then be recombined to form a hydrodesulfurized product having a sulfur content of less than 10 ppm in some embodiments.
C10G 45/02 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage
C10G 45/44 - Hydrogénation des hydrocarbures aromatiques
6.
SELECTIVE HYDRODESULFURIZATION OF FCC GASOLINE TO BELOW 10 PPM SULFUR
A process for reducing the sulfur content of a hydrocarbon stream is disclosed. A full range cracked naphtha is contacted with a hydrogenation catalyst to convert at least a portion of the dienes and mercaptans to thioethers and to hydrogenate at least a portion of the dienes. The full range cracked naphtha is fractionated into a light naphtha fraction, a medium naphtha fraction, and a heavy naphtha fraction. The heavy naphtha fraction is hydrodesulfurized. The medium naphtha fraction is mixed with hydrogen and gas oil to form a mixture, which is contacted with a hydrodesulfurization catalyst to produce a medium naphtha fraction having a reduced sulfur concentration. The light, heavy, and medium naphtha fractions may then be recombined to form a hydrodesulfurized product having a sulfur content of less than 10 ppm in some embodiments.
C10G 45/02 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage
C10G 45/44 - Hydrogénation des hydrocarbures aromatiques
7.
Selective hydrodesulfurization of FCC gasoline to below 10 ppm sulfur
A process for reducing the sulfur content of a hydrocarbon stream is disclosed. A full range cracked naphtha is contacted with a hydrogenation catalyst to convert at least a portion of the dienes and mercaptans to thioethers and to hydrogenate at least a portion of the dienes. The full range cracked naphtha is fractionated into a light naphtha fraction, a medium naphtha fraction, and a heavy naphtha fraction. The heavy naphtha fraction is hydrodesulfurized. The medium naphtha fraction is mixed with hydrogen and gas oil to form a mixture, which is contacted with a hydrodesulfurization catalyst to produce a medium naphtha fraction having a reduced sulfur concentration. The light, heavy, and medium naphtha fractions may then be recombined to form a hydrodesulfurized product having a sulfur content of less than 10 ppm in some embodiments.
C10G 65/06 - Traitement des huiles d'hydrocarbures, uniquement par plusieurs procédés d'hydrotraitement uniquement par plusieurs étapes en série ne comprenant que des étapes de raffinage au moins une étape étant une hydrogénation sélective des dioléfines
C10G 65/16 - Traitement des huiles d'hydrocarbures, uniquement par plusieurs procédés d'hydrotraitement uniquement par plusieurs étapes en parallèle ne comprenant que des étapes de raffinage
C10G 45/02 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage
C10G 45/32 - Hydrogénation sélective des composés dioléfiniques ou acétyléniques
C10G 65/00 - Traitement des huiles d'hydrocarbures, uniquement par plusieurs procédés d'hydrotraitement
A process for the production of dimethyl ether from a methanol reactor effluent is disclosed. The process may include: contacting an aqueous extractant comprising water and an effluent from a methanol synthesis reactor comprising methanol and one or more of methane, water, carbon monoxide, carbon dioxide, hydrogen, and nitrogen. At least a portion of the methanol partitions into the aqueous extractant; recovering an extract fraction comprising the aqueous extractant and methanol. The extract fraction is fed to a catalytic distillation reactor system for concurrently: contacting the methanol with catalyst in a reaction zone thereby catalytically reacting at least a portion of the methanol to form dimethyl ether and water; and fractionating the resulting dimethyl ether and the water to recover a first overheads fraction comprising dimethyl ether and a first bottoms fraction comprising water.
C07C 41/42 - SéparationPurificationStabilisationEmploi d'additifs par changement de l'état physique, p. ex. par cristallisation par distillation
B01D 3/00 - Distillation ou procédés d'échange apparentés dans lesquels des liquides sont en contact avec des milieux gazeux, p. ex. extraction
C07C 29/151 - Préparation de composés comportant des groupes hydroxyle ou O-métal liés à un atome de carbone ne faisant pas partie d'un cycle aromatique à six chaînons par réduction exclusivement des oxydes de carbone avec de l'hydrogène ou des gaz contenant de l'hydrogène
C07C 41/09 - Préparation d'éthers par déshydratation de composés contenant des groupes hydroxyle
A process and apparatus for improving the production of coke having a high volatile combustible material content are disclosed. The process may include, for example: heating a coker feedstock to a coking temperature to produce a heated coker feedstock; contacting the heated coker feedstock with a quench medium to reduce a temperature of the heated coker feedstock and produce a quenched feedstock; feeding the quenched feedstock to a coking drum; subjecting the quenched feedstock to thermal cracking in the coking drum to (a) crack a portion of the quenched feedstock to produce a cracked vapor product, and (b) produce a coke product having a volatile combustible material (VCM) concentration in the range from about 13 % to about 50 % by weight, as measured by ASTM D3175.
A process and apparatus for improving the production of coke having a high volatile combustible material content are disclosed. The process may include, for example: heating a coker feedstock to a coking temperature to produce a heated coker feedstock; contacting the heated coker feedstock with a quench medium to reduce a temperature of the heated coker feedstock and produce a quenched feedstock; feeding the quenched feedstock to a coking drum; subjecting the quenched feedstock to thermal cracking in the coking drum to (a) crack a portion of the quenched feedstock to produce a cracked vapor product, and (b) produce a coke product having a volatile combustible material (VCM) concentration in the range from about 13% to about 50% by weight, as measured by ASTM D3175.
C10G 9/14 - Craquage thermique non catalytique, en l'absence d'hydrogène, des huiles d'hydrocarbures dans des tubes ou serpentins avec ou sans dispositifs auxiliaires, p. ex. "digesteurs", chambres de maturation, dispositifs d'expansion
C10B 55/00 - Cokéfaction des huiles minérales, bitumes, goudrons ou analogues, ou de leurs mélanges, avec des matières carbonées solides
C10G 9/00 - Craquage thermique non catalytique, en l'absence d'hydrogène, des huiles d'hydrocarbures
C10B 41/00 - Dispositifs de sécurité, p. ex. dispositifs de signalisation ou de commande utilisés lors du défournement
C10B 57/04 - Autres procédés de carbonisation ou de cokéfactionCaractéristiques générales des procédés de distillation destructive utilisant des charges de composition spéciale
11.
Process and catalyst for cracking of ethers and alcohols
A process for the production of olefins from at least one of an alcohol and ether, the process including: contacting at least one alcohol or ether with a hydrofluoric acid-treated amorphous synthetic alumina-silica catalyst under decomposition conditions to produce an olefin. Also disclosed is a process for the production of isobutylene from methyl tertiary butyl ether, the process including: feeding methyl tertiary butyl ether (MTBE) to a reactor having at least one reaction zone containing a hydrofluoric acid-treated amorphous synthetic alumina-silica catalyst; contacting the MTBE with the hydrofluoric acid-treated amorphous synthetic alumina-silica catalyst under decomposition conditions to produce a reactor effluent comprising isobutylene, unreacted MTBE, heavies, and methanol; feeding the reactor effluent to a first distillation column; separating the isobutylene from the unreacted MTBE, heavies, and the methanol in the first distillation column to recover a first bottoms fraction comprising heavies, unreacted MTBE, and methanol and an isobutylene-rich overheads fraction.
C07C 1/20 - Préparation d'hydrocarbures à partir d'un ou plusieurs composés, aucun d'eux n'étant un hydrocarbure à partir de composés organiques ne renfermant que des atomes d'oxygène en tant qu'hétéro-atomes
Processes for the desulfurization of high end point naphtha, such as naphtha fractions having an ASTM D-86 end point of greater than 450°F, greater than 500°F, or greater than 550°F, and containing hindered sulfur compounds, are disclosed.
C07C 7/04 - Purification, séparation ou stabilisation d'hydrocarburesEmploi d'additifs par distillation
C10G 45/08 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage caractérisé par le catalyseur utilisé contenant du nickel ou du cobalt, ou leurs composés en combinaison avec du chrome, du molybdène ou du tungstène, ou leurs composés
C10G 65/12 - Traitement des huiles d'hydrocarbures, uniquement par plusieurs procédés d'hydrotraitement uniquement par plusieurs étapes en série comprenant des étapes de craquage et d'autres étapes d'hydrotraitement
C10G 67/02 - Traitement des huiles d'hydrocarbures, uniquement par au moins un procédé d'hydrotraitement et au moins un procédé de raffinage en l'absence d'hydrogène uniquement par plusieurs étapes en série
Processes for the desulfurization of high end point naphtha, such as naphtha fractions having an ASTM D-86 end point of greater than 450°F, greater than 500°F, or greater than 550°F, and containing hindered sulfur compounds, are disclosed.
C10G 65/12 - Traitement des huiles d'hydrocarbures, uniquement par plusieurs procédés d'hydrotraitement uniquement par plusieurs étapes en série comprenant des étapes de craquage et d'autres étapes d'hydrotraitement
C10G 45/08 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage caractérisé par le catalyseur utilisé contenant du nickel ou du cobalt, ou leurs composés en combinaison avec du chrome, du molybdène ou du tungstène, ou leurs composés
C10G 67/02 - Traitement des huiles d'hydrocarbures, uniquement par au moins un procédé d'hydrotraitement et au moins un procédé de raffinage en l'absence d'hydrogène uniquement par plusieurs étapes en série
C07C 7/04 - Purification, séparation ou stabilisation d'hydrocarburesEmploi d'additifs par distillation
A process for the production of alkylbenzene, the process including: feeding a Ci to C6 alcohol and benzene to a catalytic distillation reactor system comprising an upper reaction zone containing an alkylation catalyst and a lower reaction zone containing a transalkylation catalyst, which may be the same or different than the alkylation catalyst; concurrently in the catalytic distillation reactor system: reacting a portion of the alcohol with the benzene within the upper reaction zone to form a reaction mixture containing water, alkylbenzene, dialkyl ether, unreacted alcohol, unreacted benzene, and polyalkylate including dialkylbenzene; reacting a portion of the polyalkylate with benzene in the lower reaction zone to form additional alkylbenzene; and fractionally distilling the reaction mixture; recovering an overheads fraction from the catalytic distillation reactor system comprising benzene, unreacted alcohol, water, and dialkyl ether; recovering a bottoms fraction from the catalytic distillation reactor system comprising benzene, alkylbenzene, and polyalkylate.
C07C 2/86 - Préparation d'hydrocarbures à partir d'hydrocarbures contenant un plus petit nombre d'atomes de carbone par condensation d'un hydrocarbure et d'un non-hydrocarbure
C07C 7/04 - Purification, séparation ou stabilisation d'hydrocarburesEmploi d'additifs par distillation
B01J 8/02 - Procédés chimiques ou physiques en général, conduits en présence de fluides et de particules solidesAppareillage pour de tels procédés avec des particules immobiles, p. ex. dans des lits fixes
15.
HYDRODESULFURIZATION PROCESS WITH SELECTED LIQUID RECYCLE TO REDUCE FORMATION OF RECOMBINANT MERCAPTANS
Processes for the desulfurization of a cracked naphtha by the reaction of hydrogen with the organic sulfur compounds present in the feed are disclosed. In particular, processes disclosed herein may use one or more catalytic distillation steps followed by further hydrodesulfurization of the naphtha in a fixed bed reactor. It has been found that the formation of recombinant mercaptans in the fixed bed reactor effluent may be reduced or eliminated by reducing the concentration of hydrogen sulfide and/or olefins at the exit of the fixed bed reactor. The reduction or elimination in the formation of recombinant mercaptans may be accomplished by recycling a select portion of the fixed bed reactor effluent to the fixed bed reactor, where the select portion has a relatively low or nil concentration of olefins. Processes disclosed herein may thus facilitate the production of hydrodesulfurized cracked naphthas having a total sulfur content of less than 10 ppm, by weight.
C10G 45/02 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage
C10G 65/04 - Traitement des huiles d'hydrocarbures, uniquement par plusieurs procédés d'hydrotraitement uniquement par plusieurs étapes en série ne comprenant que des étapes de raffinage
C10G 65/06 - Traitement des huiles d'hydrocarbures, uniquement par plusieurs procédés d'hydrotraitement uniquement par plusieurs étapes en série ne comprenant que des étapes de raffinage au moins une étape étant une hydrogénation sélective des dioléfines
16.
Hydrodesulfurization process with selected liquid recycle to reduce formation of recombinant mercaptans
Processes for the desulfurization of a cracked naphtha by the reaction of hydrogen with the organic sulfur compounds present in the feed are disclosed. In particular, processes disclosed herein may use one or more catalytic distillation steps followed by further hydrodesulfurization of the naphtha in a fixed bed reactor. It has been found that the formation of recombinant mercaptans in the fixed bed reactor effluent may be reduced or eliminated by reducing the concentration of hydrogen sulfide and/or olefins at the exit of the fixed bed reactor. The reduction or elimination in the formation of recombinant mercaptans may be accomplished by recycling a select portion of the fixed bed reactor effluent to the fixed bed reactor, where the select portion has a relatively low or nil concentration of olefins. Processes disclosed herein may thus facilitate the production of hydrodesulfurized cracked naphthas having a total sulfur content of less than 10 ppm, by weight.
Processes for the desulfurization of a cracked naphtha by the reaction of hydrogen with the organic sulfur compounds present in the feed are disclosed. In particular, processes disclosed herein may use one or more catalytic distillation steps followed by further hydrodesulfurization of the naphtha in a fixed bed reactor. It has been found that the formation of recombinant mercaptans in the fixed bed reactor effluent may be reduced or eliminated by reducing the concentration of hydrogen sulfide and/or olefins at the exit of the fixed bed reactor. The reduction or elimination in the formation of recombinant mercaptans may be accomplished by recycling a select portion of the fixed bed reactor effluent to the fixed bed reactor, where the select portion has a relatively low or nil concentration of olefins. Processes disclosed herein may thus facilitate the production of hydrodesulfurized cracked naphthas having a total sulfur content of less than 10 ppm, by weight.
C10G 65/04 - Traitement des huiles d'hydrocarbures, uniquement par plusieurs procédés d'hydrotraitement uniquement par plusieurs étapes en série ne comprenant que des étapes de raffinage
C10G 45/02 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage
C10G 65/06 - Traitement des huiles d'hydrocarbures, uniquement par plusieurs procédés d'hydrotraitement uniquement par plusieurs étapes en série ne comprenant que des étapes de raffinage au moins une étape étant une hydrogénation sélective des dioléfines
18.
Process to hydrodesulfurize FCC gasoline resulting in a low-mercaptan product
C10G 45/02 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage
19.
PRODUCTION OF JET AND OTHER HEAVY FUELS FROM ISOBUTANOL
A process for the production of jet and other heavy fuels, the process including: contacting at least one C3 to C5 isoalkanol with a first catalyst to convert at least a portion of the isoalkanol to isoalkene, isoalkene dimers, and water; contacting at least a portion of the isoalkene dimers with a second catalyst to convert at least a portion of the isoalkene dimers to isoalkene trimers; hydrotreating the isoalkene trimers to form isoalkanes useful as a jet fuel, kerosene, or other heavy fuels.
B01J 31/06 - Catalyseurs contenant des hydrures, des complexes de coordination ou des composés organiques contenant des composés organiques ou des hydrures métalliques contenant des polymères
C07C 1/20 - Préparation d'hydrocarbures à partir d'un ou plusieurs composés, aucun d'eux n'étant un hydrocarbure à partir de composés organiques ne renfermant que des atomes d'oxygène en tant qu'hétéro-atomes
C07C 2/00 - Préparation d'hydrocarbures à partir d'hydrocarbures contenant un plus petit nombre d'atomes de carbone
C10G 45/04 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage caractérisé par le catalyseur utilisé
C10L 1/04 - Combustibles carbonés liquides à base essentielle de mélanges d'hydrocarbures
20.
Production of jet and other heavy fuels from isobutanol
A process for the production of jet and other heavy fuels, the process including: contacting at least one C3 to C5 isoalkanol with a first catalyst to convert at least a portion of the isoalkanol to isoalkene, isoalkene dimers, and water; contacting at least a portion of the isoalkene dimers with a second catalyst to convert at least a portion of the isoalkene dimers to isoalkene trimers; hydrotreating the isoalkene trimers to form isoalkanes useful as a jet fuel, kerosene, or other heavy fuels.
C07C 1/24 - Préparation d'hydrocarbures à partir d'un ou plusieurs composés, aucun d'eux n'étant un hydrocarbure à partir de composés organiques ne renfermant que des atomes d'oxygène en tant qu'hétéro-atomes par élimination d'eau
C07C 2/04 - Préparation d'hydrocarbures à partir d'hydrocarbures contenant un plus petit nombre d'atomes de carbone par addition d'hydrocarbures non saturés entre eux par oligomérisation d'hydrocarbures non saturés bien définis, sans formation de cycle
C07C 5/03 - Préparation d'hydrocarbures à partir d'hydrocarbures contenant le même nombre d'atomes de carbone par hydrogénation de liaisons doubles carbone-carbone non aromatiques
C07C 2/12 - Procédés catalytiques avec des alumino-silicates cristallins, p. ex. avec des tamis moléculaires
C07C 2/28 - Procédés catalytiques avec des hydrures ou des composés organiques avec des résines échangeuses d'ions
C10G 3/00 - Production de mélanges liquides d'hydrocarbures à partir de matières organiques contenant de l'oxygène, p. ex. huiles, acides gras
C10G 69/12 - Traitement des huiles d'hydrocarbures par au moins un procédé d'hydrotraitement et au moins un autre procédé de conversion uniquement par plusieurs étapes en série comprenant au moins une étape de polymérisation ou d'alkylation
21.
PRODUCTION OF JET AND OTHER HEAVY FUELS FROM ISOBUTANOL
A process for the production of jet and other heavy fuels, the process including: contacting at least one C3 to C5 isoalkanol with a first catalyst to convert at least a portion of the isoalkanol to isoalkene, isoalkene dimers, and water; contacting at least a portion of the isoalkene dimers with a second catalyst to convert at least a portion of the isoalkene dimers to isoalkene trimers; hydrotreating the isoalkene trimers to form isoalkanes useful as a jet fuel, kerosene, or other heavy fuels.
C07C 2/00 - Préparation d'hydrocarbures à partir d'hydrocarbures contenant un plus petit nombre d'atomes de carbone
C07C 1/20 - Préparation d'hydrocarbures à partir d'un ou plusieurs composés, aucun d'eux n'étant un hydrocarbure à partir de composés organiques ne renfermant que des atomes d'oxygène en tant qu'hétéro-atomes
C10L 1/04 - Combustibles carbonés liquides à base essentielle de mélanges d'hydrocarbures
C10G 45/04 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage caractérisé par le catalyseur utilisé
B01J 31/06 - Catalyseurs contenant des hydrures, des complexes de coordination ou des composés organiques contenant des composés organiques ou des hydrures métalliques contenant des polymères
22.
Gasoline hydrodesulfurization and membrane unit to reduce mercaptan type sulfur
A process for the hydrodesulfurization of gasoline is disclosed, the process including: feeding (1) a cracked naphtha containing mercaptans and other organic sulfur compounds and (2) hydrogen to a first hydrodesulfurization reactor containing one or more beds of a hydrodesulfurization catalyst; contacting sulfur compounds comprising the other organic sulfur compounds in the cracked naphtha with hydrogen in the presence of a hydrodesulfurization catalyst to convert a portion of the other organic sulfur compounds to hydrogen sulfide; withdrawing from the hydrodesulfurization reactor an effluent comprising hydrocarbons and hydrogen sulfide. The effluent from the hydrodesulfurization reactor is fed to a membrane separation system containing a membrane for partitioning the hydrocarbons from the hydrogen sulfide. For example, the membrane may be selective to hydrogen sulfide, to separate a permeate fraction comprising hydrogen sulfide from a residue fraction comprising the hydrocarbons.
C10G 31/09 - Raffinage des huiles d'hydrocarbures, en l'absence d'hydrogène, par des méthodes non prévues ailleurs par filtration
C10G 45/02 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage
23.
GASOLINE HYDRODESULFURIZATION AND MEMBRANE UNIT TO REDUCE MERCAPTAN TYPE SULFUR
A process for the hydrodesulfurization of gasoline is disclosed, the process including: feeding (1) a cracked naphtha containing mercaptans and other organic sulfur compounds and (2) hydrogen to a first hydrodesulfurization reactor containing one or more beds of a hydrodesulfurization catalyst; contacting sulfur compounds comprising the other organic sulfur compounds in the cracked naphtha with hydrogen in the presence of a hydrodesulfurization catalyst to convert a portion of the other organic sulfur compounds to hydrogen sulfide; withdrawing from the hydrodesulfurization reactor an effluent comprising hydrocarbons and hydrogen sulfide. The effluent from the hydrodesulfurization reactor is fed to a membrane separation system containing a membrane for partitioning the hydrocarbons from the hydrogen sulfide. For example, the membrane may be selective to hydrogen sulfide, to separate a permeate fraction comprising hydrogen sulfide from a residue fraction comprising the hydrocarbons.
C10G 67/02 - Traitement des huiles d'hydrocarbures, uniquement par au moins un procédé d'hydrotraitement et au moins un procédé de raffinage en l'absence d'hydrogène uniquement par plusieurs étapes en série
B01D 61/00 - Procédés de séparation utilisant des membranes semi-perméables, p. ex. dialyse, osmose ou ultrafiltrationAppareils, accessoires ou opérations auxiliaires, spécialement adaptés à cet effet
C10G 45/00 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène
A process for the conversion of an alcohol to an olefin is disclosed. The process may include: contacting at least one C2 to C 5 alcohol with an organic acid in the presence of an esterification catalyst to convert at least a portion of the at least one C2 to C5 alcohol and the organic acid to an ester; at least one of catalytically and thermally degrading the ester to form an organic acid and an olefin.
C07C 1/20 - Préparation d'hydrocarbures à partir d'un ou plusieurs composés, aucun d'eux n'étant un hydrocarbure à partir de composés organiques ne renfermant que des atomes d'oxygène en tant qu'hétéro-atomes
A process for the conversion of an alcohol to an olefin is disclosed. The process may include: contacting at least one C2 to C5 alcohol with an organic acid in the presence of an esterification catalyst to convert at least a portion of the at least one C2 to C5 alcohol and the organic acid to an ester; at least one of catalytically and thermally degrading the ester to form an organic acid and an olefin.
C07C 1/213 - Préparation d'hydrocarbures à partir d'un ou plusieurs composés, aucun d'eux n'étant un hydrocarbure à partir de composés organiques ne renfermant que des atomes d'oxygène en tant qu'hétéro-atomes à partir de composés carbonylés par scission d'esters
Processes for the alcoholysis, inclusive of transesterification and/or disproportionation, of reactants are disclosed. The alcoholysis process may include feeding reactants and a trace amount of soluble organometallic compound to a reactor comprising a solid alcoholysis catalyst, wherein the soluble organometallic compound and the solid alcoholysis catalyst each independently comprise a Group II to Group VI element, which may be the same element in various embodiments. As an example, diphenyl carbonate may be continuously produced by performing transesterification over a solid catalyst followed by disproportionation, where a trace amount of soluble organometallic compound is fed to the transesterification reactor. Also disclosed is a process for reactivating a spent solid alcoholysis catalyst, such as a catalyst useful for transesterifications and/or disproportionations, the process including removing polymeric materials deposited on the catalyst and re-depositing catalytically active metals on the solid catalyst.
A process for the dimerization of isoolefins is disclosed. The process may include: contacting an isoolefin with sulfurous acid in a reaction zone at conditions of temperature and pressure sufficient to dimerize at least a portion of the isoolefin.
A process for the production of dimethyl ether from a methanol reactor effluent is disclosed. The process may include: contacting an aqueous extractant comprising water and an effluent from a methanol synthesis reactor comprising methanol and one or more of methane, water, carbon monoxide, carbon dioxide, hydrogen, and nitrogen. At least a portion of the methanol partitions into the aqueous extractant; recovering an extract fraction comprising the aqueous extractant and methanol. The extract fraction is fed to a catalytic distillation reactor system for concurrently: contacting the methanol with catalyst in a reaction zone thereby catalytically reacting at least a portion of the methanol to form dimethyl ether and water; and fractionating the resulting dimethyl ether and the water to recover a first overheads fraction comprising dimethyl ether and a first bottoms fraction comprising water.
B01J 8/02 - Procédés chimiques ou physiques en général, conduits en présence de fluides et de particules solidesAppareillage pour de tels procédés avec des particules immobiles, p. ex. dans des lits fixes
A process for the production of dimethyl ether from a methanol reactor effluent is disclosed. The process may include: contacting an aqueous extractant comprising water and an effluent from a methanol synthesis reactor comprising methanol and one or more of methane, water, carbon monoxide, carbon dioxide, hydrogen, and nitrogen. At least a portion of the methanol partitions into the aqueous extractant; recovering an extract fraction comprising the aqueous extractant and methanol. The extract fraction is fed to a catalytic distillation reactor system for concurrently: contacting the methanol with catalyst in a reaction zone thereby catalytically reacting at least a portion of the methanol to form dimethyl ether and water; and fractionating the resulting dimethyl ether and the water to recover a first overheads fraction comprising dimethyl ether and a first bottoms fraction comprising water.
A process for recovering benzene, the process including: feeding hydrogen and a hydrocarbon fraction comprising benzene, components lighter than benzene, components heavier than benzene, and diolefins to a catalytic distillation reactor system comprising at least one reaction zone comprising a hydrogenation catalyst; concurrently in the catalytic distillation reactor system: contacting the diolefins and hydrogen in the presence of the hydrogenation catalyst to selectively hydrogenate at least a portion of the diolefins; and fractionating the hydrocarbon fraction to form a fraction comprising benzene and other C6 hydrocarbons, and a heavies fraction comprising C7+ hydrocarbons; recovering the heavies fraction from the first catalytic distillation reactor system as a bottoms fraction; and withdrawing the fraction comprising benzene and other C6 hydrocarbons from the catalytic distillation reactor system as a benzene concentrate fraction.
C07C 7/04 - Purification, séparation ou stabilisation d'hydrocarburesEmploi d'additifs par distillation
C07C 5/10 - Préparation d'hydrocarbures à partir d'hydrocarbures contenant le même nombre d'atomes de carbone par hydrogénation de cycles aromatiques à six chaînons
B01J 8/02 - Procédés chimiques ou physiques en général, conduits en présence de fluides et de particules solidesAppareillage pour de tels procédés avec des particules immobiles, p. ex. dans des lits fixes
C07C 5/09 - Préparation d'hydrocarbures à partir d'hydrocarbures contenant le même nombre d'atomes de carbone par hydrogénation de liaisons triples carbone-carbone en liaisons doubles carbone-carbone
A process for fractionating isobutene from normal butenes, including: introducing hydrogen and a feed stream comprising isobutene, 1-butene, and 2-butene into a first column including a reaction zone containing a hydroisomerization catalyst operating at a first pressure and concurrently: (i) converting at least a portion of the 1-butene to 2-butene, and (ii) separating isobutene from the 2-butene; recovering a first overheads fraction comprising isobutene from the first column; recovering a first bottoms fraction comprising isobutene, 2-butene, and unreacted 1-butene from the first column; introducing the first bottoms fraction into a top portion of a second column comprising a fractionation column operating at a second pressure lower than the first pressure; separating the first bottoms into a second overheads fraction comprising isobutene and 1-butene and a second bottoms fraction comprising 2-butene; compressing the second overheads fraction; and introducing the compressed second overheads fraction to a lower portion of the first column.
A process for fractionating isobutene from normal butenes, including: introducing hydrogen and a feed stream comprising isobutene, 1-butene, and 2-butene into a first column including a reaction zone containing a hydroisomerization catalyst operating at a first pressure and concurrently: (i) converting at least a portion of the 1-butene to 2-butene, and (ii) separating isobutene from the 2-butene; recovering a first overheads fraction comprising isobutene from the first column; recovering a first bottoms fraction comprising isobutene, 2-butene, and unreacted 1-butene from the first column; introducing the first bottoms fraction into a top portion of a second column comprising a fractionation column operating at a second pressure lower than the first pressure; separating the first bottoms into a second overheads fraction comprising isobutene and 1-butene and a second bottoms fraction comprising 2-butene; compressing the second overheads fraction; and introducing the compressed second overheads fraction to a lower portion of the first column.
A process for the dimerization of isoolefins, including: contacting an isoolefin with a solid catalyst composition passivated with at least one of an ether, an alcohol, and water; wherein the solid catalyst composition comprises at least one of a solid phosphoric acid catalyst and a resin of a macroporous matrix of polyvinyl aromatic compound crosslinked with a divinyl compound and having thereon from about 3 to 5 milli equivalents of sulfonic acid groups per gram of dry resin; and wherein at least 50% to less than 100% of acid groups in the solid catalyst composition are neutralized with a metal of Al, Fe, Zn, Cu, Ni, or mixtures thereof. The catalyst may be metalized prior to placement in a reactor or may be metalized in situ.
C07C 2/04 - Préparation d'hydrocarbures à partir d'hydrocarbures contenant un plus petit nombre d'atomes de carbone par addition d'hydrocarbures non saturés entre eux par oligomérisation d'hydrocarbures non saturés bien définis, sans formation de cycle
A process for oligomerization of isobutene, the process including: feeding a hydrocarbon stream comprising n-butane, 1-butene, 2-butene, isobutane, and isobutene to a catalytic distillation reactor system comprising a hydroisomerization catalyst; feeding hydrogen to the catalytic distillation reactor system; concurrently in the catalytic distillation reactor system: contacting the 1-butene with the hydrogen in the presence of the hydroisomerization catalyst to convert at least a portion of the 1-butene to 2-butene; separating the isobutane and the isobutene from the n-butane and the 2-butene; recovering the isobutane and the isobutene from the catalytic distillation reactor system as an overheads fraction; recovering the n-butane and the 2-butene from the catalytic distillation reactor system as a bottoms fraction; contacting the overheads fraction in an oligomerization reaction system with an oligomerization catalyst to convert a portion of the isobutene to oligomers.
A process for oligomerization of isobutene, the process including: feeding a hydrocarbon stream comprising n-butane, 1-butene, 2-butene, isobutane, and isobutene to a catalytic distillation reactor system comprising a hydroisomerization catalyst; feeding hydrogen to the catalytic distillation reactor system; concurrently in the catalytic distillation reactor system: contacting the 1-butene with the hydrogen in the presence of the hydroisomerization catalyst to convert at least a portion of the 1-butene to 2-butene; separating the isobutane and the isobutene from the n-butane and the 2-butene; recovering the isobutane and the isobutene from the catalytic distillation reactor system as an overheads fraction; recovering the n-butane and the 2-butene from the catalytic distillation reactor system as a bottoms fraction; contacting the overheads fraction in an oligomerization reaction system with an oligomerization catalyst to convert a portion of the isobutene to oligomers.
C07C 2/06 - Préparation d'hydrocarbures à partir d'hydrocarbures contenant un plus petit nombre d'atomes de carbone par addition d'hydrocarbures non saturés entre eux par oligomérisation d'hydrocarbures non saturés bien définis, sans formation de cycle d'alcènes, c.-à-d. d'hydrocarbures acycliques ne comportant qu'une seule liaison double carbone-carbone
C07C 5/25 - Déplacement de liaisons doubles carbone-carbone
A process for the regeneration of spent sulfuric acid including contacting spent sulfuric acid containing acid soluble oils (ASO) with sulfur dioxide to extract at least a portion of the ASO from the spent sulfuric acid into the sulfur dioxide. The sulfuric acid phase having a reduced ASO content and a sulfur dioxide phase containing at least a portion of the ASO may be recovered. The resulting sulfuric acid and sulfur dioxide phases may be further separated to recover ASO, sulfur dioxide, and sulfuric acid.
A process for oligomerizing isoolefins, the process including: feeding an isoolefm to an oligomerization reaction zone; feeding an oxygen-containing reaction moderator to the oligomerization reaction zone; concurrently in the oligomerization reaction zone: contacting the isoolefin with an oligomerization catalyst to convert at least a portion of the isoolefin to oligomers comprising dimers and trimers of the isoolefin; reacting a portion of the moderator with a portion of at least one of the isoolefin and the oligomers to form an oxygenated oligomerization byproduct; recovering an effluent from the oligomerization reaction zone comprising the oligomers and the oxygenated oligomerization byproduct; fractionating at least a portion of the effluent to recover a fraction comprising the oxygenated oligomerization byproduct and the trimers and a fraction comprising the dimers.
C10G 50/00 - Production de mélanges d'hydrocarbures liquides à partir d'hydrocarbures à nombre inférieur d'atomes de carbone, p. ex. par oligomérisation
A process for oligomerizing isoolefins, the process including: feeding an isoolefin to an oligomerization reaction zone; feeding an oxygen-containing reaction moderator to the oligomerization reaction zone; concurrently in the oligomerization reaction zone: contacting the isoolefin with an oligomerization catalyst to convert at least a portion of the isoolefin to oligomers comprising dimers and trimers of the isoolefin; reacting a portion of the moderator with a portion of at least one of the isoolefin and the oligomers to form an oxygenated oligomerization byproduct; recovering an effluent from the oligomerization reaction zone comprising the oligomers and the oxygenated oligomerization byproduct; fractionating at least a portion of the effluent to recover a fraction comprising the oxygenated oligomerization byproduct and the trimers and a fraction comprising the dimers.
C07C 2/28 - Procédés catalytiques avec des hydrures ou des composés organiques avec des résines échangeuses d'ions
C07C 29/04 - Préparation de composés comportant des groupes hydroxyle ou O-métal liés à un atome de carbone ne faisant pas partie d'un cycle aromatique à six chaînons par addition de groupes hydroxyle à des liaisons carbone-carbone non saturées, p. ex. à l'aide de H2O2 par hydratation de liaisons doubles carbone-carbone
C10L 1/02 - Combustibles carbonés liquides à base essentielle de composants formés uniquement de carbone, d'hydrogène et d'oxygène
C10G 69/12 - Traitement des huiles d'hydrocarbures par au moins un procédé d'hydrotraitement et au moins un autre procédé de conversion uniquement par plusieurs étapes en série comprenant au moins une étape de polymérisation ou d'alkylation
C10G 50/00 - Production de mélanges d'hydrocarbures liquides à partir d'hydrocarbures à nombre inférieur d'atomes de carbone, p. ex. par oligomérisation
C07C 41/06 - Préparation d'éthers par addition de composés à des composés non saturés uniquement par addition de composés organiques
A process for treating an alkylation feedstock comprising olefins, n-alkanes, iso-alkanes, and impurities including one or more of butadiene, oxygenates, nitrogen- containing compounds, and sulfur-containing compounds, the process including: contacting an alkylation feedstock containing at least one of oxygenates and nitrogen-containing compounds with water to produce a hydrocarbon fraction having a reduced concentration of the at least one of oxygenates and nitrogen-containing compounds and an aqueous fraction comprising at least a portion of the at least one of oxygenates and nitrogen-containing compounds; separating water from the hydrocarbon fraction having a reduced concentration to produce a hydrocarbon fraction having a reduced water content; contacting the hydrocarbon fraction having a reduced water content with an oligomerization catalyst in a first oligomerization reaction zone under oligomerization conditions to react at least a portion of the olefins to form a reactor effluent comprising olefin oligomers; and feeding at least a portion of the reactor effluent to an alkylation unit.
C10G 69/12 - Traitement des huiles d'hydrocarbures par au moins un procédé d'hydrotraitement et au moins un autre procédé de conversion uniquement par plusieurs étapes en série comprenant au moins une étape de polymérisation ou d'alkylation
C10G 27/02 - Raffinage des huiles d'hydrocarbures, en l'absence d'hydrogène, par oxydation avec un halogène ou des composés donneurs d'halogèneAcide hypochloreux ou ses sels
C10G 27/04 - Raffinage des huiles d'hydrocarbures, en l'absence d'hydrogène, par oxydation avec de l'oxygène ou des composés donnant de l'oxygène
C10G 25/03 - Raffinage des huiles d'hydrocarbures, en l'absence d'hydrogène, au moyen d'absorbants ou d'adsorbants solides avec échangeur d'ions avec des alumino-silicates cristallins, p. ex. avec des tamis moléculaires
C07C 7/05 - Purification, séparation ou stabilisation d'hydrocarburesEmploi d'additifs par distillation à l'aide de composés auxiliaires
C07C 7/13 - Purification, séparation ou stabilisation d'hydrocarburesEmploi d'additifs par adsorption, c.-à-d. purification ou séparation d'hydrocarbures à l'aide de solides, p. ex. à l'aide d'échangeurs d'ions par la technique du tamis moléculaire
A process for treating an alkylation feedstock comprising olefins, n-alkanes, iso-alkanes, and impurities including one or more of butadiene, oxygenates, nitrogen-containing compounds, and sulfur-containing compounds, the process including: contacting an alkylation feedstock containing at least one of oxygenates and nitrogen-containing compounds with water to produce a hydrocarbon fraction having a reduced concentration of the at least one of oxygenates and nitrogen-containing compounds and an aqueous fraction comprising at least a portion of the at least one of oxygenates and nitrogen-containing compounds; separating water from the hydrocarbon fraction having a reduced concentration to produce a hydrocarbon fraction having a reduced water content; contacting the hydrocarbon fraction having a reduced water content with an oligomerization catalyst in a first oligomerization reaction zone under oligomerization conditions to react at least a portion of the olefins to form a reactor effluent comprising olefin oligomers; and feeding at least a portion of the reactor effluent to an alkylation unit.
C07C 2/06 - Préparation d'hydrocarbures à partir d'hydrocarbures contenant un plus petit nombre d'atomes de carbone par addition d'hydrocarbures non saturés entre eux par oligomérisation d'hydrocarbures non saturés bien définis, sans formation de cycle d'alcènes, c.-à-d. d'hydrocarbures acycliques ne comportant qu'une seule liaison double carbone-carbone
C07C 2/56 - Addition à des hydrocarbures acycliques
43.
Process for the alkylation of isobutane with dilute propylene
A process for alkylation of propylene, the process including: contacting a stream comprising propylene and propane with sulfuric acid in a first reaction zone under conditions to form propylene sulfate esters; contacting the propylene sulfate esters with isoparaffin and sulfuric acid in an alkylation reaction zone under conditions to react the propylene sulfate esters and the isoparaffin to form a reactor effluent comprising an acid phase and a hydrocarbon phase comprising unreacted isoparaffin and alkylate product; separating the hydrocarbon phase from the sulfuric acid; separating the hydrocarbon phase to form a fraction comprising unreacted isoparaffin and a fraction comprising the alkylate product.
A process for alkylation of propylene, the process including: contacting a stream comprising propylene and propane with sulfuric acid in a first reaction zone under conditions to form propylene sulfate esters; contacting the propylene sulfate esters with isoparaffin and sulfuric acid in an alkylation reaction zone under conditions to react the propylene sulfate esters and the isoparaffin to form a reactor effluent comprising an acid phase and a hydrocarbon phase comprising unreacted isoparaffin and alkylate product; separating the hydrocarbon phase from the sulfuric acid; separating the hydrocarbon phase to form a fraction comprising unreacted isoparaffin and a fraction comprising the alkylate product.
C07C 5/03 - Préparation d'hydrocarbures à partir d'hydrocarbures contenant le même nombre d'atomes de carbone par hydrogénation de liaisons doubles carbone-carbone non aromatiques
A process for reducing the concentration of benzene in a hydrocarbon stream, the process including: fractionating a reformate to form a benzene concentrate fraction comprising benzene and other C6 hydrocarbons, and a heavies fraction comprising C7+ hydrocarbons; and hydrogenating the benzene concentrate fraction to form a hydrocarbon fraction having a reduced benzene concentration.
C10G 69/04 - Traitement des huiles d'hydrocarbures par au moins un procédé d'hydrotraitement et au moins un autre procédé de conversion uniquement par plusieurs étapes en série comprenant au moins une étape de craquage catalytique en l'absence d'hydrogène
C10G 45/02 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage
C07C 7/163 - Purification, séparation ou stabilisation d'hydrocarburesEmploi d'additifs par traitement provoquant une modification chimique d'au moins un composé par hydrogénation
C10G 45/44 - Hydrogénation des hydrocarbures aromatiques
C10G 65/04 - Traitement des huiles d'hydrocarbures, uniquement par plusieurs procédés d'hydrotraitement uniquement par plusieurs étapes en série ne comprenant que des étapes de raffinage
4 olefins, heavy hydrocarbons, and the catalyst; separating the catalyst from the effluent; separating the benzene from the monoalkylate product and the heavy hydrocarbons within the liquid effluent; separating the monoalkylate product from the heavy hydrocarbons within the liquid effluent; and recovering the monoalkylate product.
C07C 6/12 - Préparation d'hydrocarbures à partir d'hydrocarbures contenant un nombre différent d'atomes de carbone par des réactions de redistribution par conversion d'une liaison carbone-carbone saturée exclusivement dans les hydrocarbures contenant un cycle aromatique à six chaînons
A process for reducing benzene content in a reformate stream, including: fractionating a full range reformate comprising benzene, C7 to C9 monoalkyl aromatics, and C1O+ polyalkyl aromatics into at least three fractions including a light reformate fraction comprising the benzene; a medium reformate fraction comprising the C7 to C9 monoalkyl aromatics; and a heavy reformate fraction comprising the C10+ polyalkyl aromatics; feeding the light reformate fraction, the heavy reformate fraction and a transalkylation catalyst to a transalkylation reaction zone; contacting the light fraction and the heavy fraction in presence of the transalkylation catalyst in the transalkylation reaction zone to react at least a portion of the benzene with C1O+ polyalkyl aromatics to form monoalkyl aromatics; separating an effluent from the transalkylation reaction zone to form a catalyst fraction and a liquid fraction comprising the monoalkyl aromatics.
A process for alkylation of benzene, including: feeding benzene, a polyalkylate, and a catalyst to a reactor comprising a first and a second reaction zone; reacting the benzene and the polyalkylate in the first reaction zone under transalkylation conditions to form a monoalkylate product; feeding a C2-C4 olefin to the reactor intermediate the first and second reaction zones; reacting benzene and the C2-C4 olefin in the second reaction zone under alkylation conditions to form additional monoalkylate product; recovering an effluent from the reactor, wherein the effluent comprises benzene, the monoalkylate product, any unreacted C2-C4 olefins, heavy hydrocarbons, and the catalyst; separating the catalyst from the effluent; separating the benzene from the monoalkylate product and the heavy hydrocarbons within the liquid effluent; separating the monoalkylate product from the heavy hydrocarbons within the liquid effluent; and recovering the monoalkylate product.
C07C 5/03 - Préparation d'hydrocarbures à partir d'hydrocarbures contenant le même nombre d'atomes de carbone par hydrogénation de liaisons doubles carbone-carbone non aromatiques
Catalytic Distillation Technologies, Chemical Research & Licensing Company, a Texas Corporation and Lummus Technology LLC, a Delaware Limited Liability Company ()
Column packing for reactive distillation columns, namely, mesh wire with a multi-filament component or expanded metal intertwined with a multi-filament component, the multi-filament selected from inert polymers, catalytic polymers, catalytic metals or mixtures thereof for producing alkylate in a sulfuric acid alkylation
5 olefins; fractionating the dilute alkylate product to form an isobutane-rich fraction, a n-butane-rich fraction, a fraction containing isopentane, and an alkylate product having a Reid vapor pressure less than 0.35 bar (5 psi); recycling at least a portion of the fraction containing isopentane to the alkylation reactor.
C07C 2/02 - Préparation d'hydrocarbures à partir d'hydrocarbures contenant un plus petit nombre d'atomes de carbone par addition d'hydrocarbures non saturés entre eux
A process for the production of ethylene, the process including: feeding hydrogen, a heavy solvent, a light solvent, and acetylene to a down-flow reactor comprising at least one reaction zone comprising a hydrogenation catalyst; concurrently in the down-flow reactor: contacting acetylene and hydrogen in the presence of the hydrogenation catalyst to convert at least a portion of the acetylene to ethylene; boiling at least a portion of the light solvent from a liquid phase to a vapor phase; recovering a reactor effluent comprising heavy solvent, light solvent, and ethylene; condensing at least a portion of the light solvent in the vapor phase; recovering a solvent fraction comprising the heavy solvent and the light solvent; recovering a product fraction comprising ethylene.
C07C 5/09 - Préparation d'hydrocarbures à partir d'hydrocarbures contenant le même nombre d'atomes de carbone par hydrogénation de liaisons triples carbone-carbone en liaisons doubles carbone-carbone
53.
CATALYST AND PROCESS FOR THE SELECTIVE HYDRODESULFURIZATION OF AN OLEFIN CONTAINING HYDROCARBON FEEDSTOCK
A catalyst composition having a low surface area of less than 100 m2/g and a high mean pore diameter of greater than 200 A, wherein the catalyst composition comprises a cobalt component, a molybdenum component, a phosphorus component and an alumina support which support is predominantly in the form of theta-alumina and delta-alumina. The catalyst composition is highly active toward the hydrodesulfurization of an olef in-containing feedstock having a sulfur concentration while being selective toward the hydrogenation of the olefins contained in the feedstock and is used in a novel process for the selective desulfurization of an olef in-containing feedstock.
C10G 45/36 - Hydrogénation sélective des composés dioléfiniques ou acétyléniques caractérisée par le catalyseur utilisé contenant du nickel ou du cobalt, ou leurs composés
A process for selective hydrodesulfurization of a sulfur and olef in-containing hydrocarbon feedstock boiling in the naphtha or gasoline boiling range utilizing a particularly defined high activity hydrodesulfurization (HDS) catalyst composition comprising a cobalt component, a molybdenum component and little or no phosphorus, prepared on a special alumina support containing a low concentration of silica and having a high surface area of at least 280 m2/g. In another aspect the process involves separating the feedstock into a light and a heavy fraction, followed by selectively hydrodesulfurizing the heavy fraction using a particularly defined high activity HDS catalyst and hydrodesulfurizing the light fraction with a particularly defined high selectivity HDS catalyst. The process also includes performing the separation into fractions and the selective hydrodesulfurization of the fractions in a distillation column reactor utilizing different particularly defined HDS catalysts.
C10G 45/06 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage caractérisé par le catalyseur utilisé contenant du nickel ou du cobalt, ou leurs composés
C10G 45/08 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage caractérisé par le catalyseur utilisé contenant du nickel ou du cobalt, ou leurs composés en combinaison avec du chrome, du molybdène ou du tungstène, ou leurs composés
A process for the reduction of benzene in a gasoline stream, the process including: feeding a gasoline fraction including benzene and C6+ hydrocarbons and at least one of an alcohol and an ether to a catalytic distillation column comprising at least one reaction zone containing an alkylation catalyst, wherein the at least one reaction zone is above a gasoline fraction feed location; concurrently in the catalytic distillation column: separating the C6 hydrocarbons from C7+ hydrocarbons, wherein the C6 hydrocarbons and benzene distill upward into the at least one reaction zone; contacting benzene and the at least one of an alcohol and an ether in the at least one reaction zone in the presence of the alkylation catalyst to convert at least a portion of the benzene and alcohol /ether to an alkylate; recovering an overheads fraction including C6 hydrocarbons, any unreacted alcohol and ether, and water; and recovering a bottoms fraction including C7+ hydrocarbons and the alkylate.
C10G 55/06 - Traitement des huiles d'hydrocarbures, en l'absence d'hydrogène, par au moins un procédé de raffinage et par au moins un procédé de craquage uniquement par plusieurs étapes en série comprenant au moins une étape de craquage catalytique
Processes for the alcoholysis, inclusive of transesterification and/or disproportionation, of reactants are disclosed. The alcoholysis process may include feeding reactants and a trace amount of soluble organometallic compound to a reactor comprising a solid alcoholysis catalyst, wherein the soluble organometallic compound and the solid alcoholysis catalyst each independently comprise a Group II to Group VI element, which may be the same element in various embodiments. As an example, diphenyl carbonate may be continuously produced by performing transesterification over a solid catalyst followed by disproportionation, where a trace amount of soluble organometallic compound is fed to the transesterification reactor. Also disclosed is a process for reactivating a spent solid alcoholysis catalyst, such as a catalyst useful for transesterifications and/or disproportionations, the process including removing polymeric materials deposited on the catalyst and re-depositing catalytically active metals on the solid catalyst.
C07C 68/06 - Préparation des esters de l'acide carbonique ou de l'acide formique halogéné à partir de carbonates organiques
C11C 3/00 - Graisses, huiles ou acides gras obtenus par transformation chimique des graisses, huiles ou acides gras, p. ex. ozonolyse
B01J 31/38 - Catalyseurs contenant des hydrures, des complexes de coordination ou des composés organiques contenant en outre des composés métalliques inorganiques non prévus dans les groupes du titane, du zirconium ou du hafnium
B01J 31/12 - Catalyseurs contenant des hydrures, des complexes de coordination ou des composés organiques contenant des composés organiques ou des hydrures métalliques contenant des composés organométalliques ou des hydrures métalliques
C07C 269/00 - Préparation de dérivés d'acide carbamique, c.-à-d. de composés contenant l'un des groupes l'atome d'azote ne faisant pas partie de groupes nitro ou nitroso
58.
PROCESS TO PRODUCE CLEAN GASOLINE/BIO-ETHERS USING ETHANOL
A fuel or fuel blendstock comprising ethanol, ethyl ethers, olefins, and alkanes. In some embodiments, the fuel or fuel blendstock of claim 1, wherein the fuel or fuel blendstock may have an octane number greater than 92 (RON + MON)/2). In other embodiments, the fuel or fuel blendstock may have a Reid vapor pressure less than 7.2 psi. Also disclosed is a process for the production of a fuel, the process including: contacting ethanol and at least one gasoline fraction including alkanes and olefins in the presence of a catalyst to form a fuel mixture including ethyl ethers, alkanes, unreacted olefins, and unreacted ethanol; and recovering the fuel mixture for use as a gasoline or gasoline blendstock without separation of the ethanol from the fuel mixture.
A process for the desulfurization of a fluid catalytically cracked naphtha wherein the valuable olefins are retained and recombinant mercaptans are prevented from forming, resulting in a low sulfur naphtha. Embodiments disclosed herein may allow for more flexibility in varying the end point of the naphtha used in gasoline blending
C10G 51/04 - Traitement des huiles d'hydrocarbures, en l'absence d'hydrogène, uniquement par plusieurs procédés de craquage uniquement par plusieurs étapes en série ne comprenant que des étapes de craquage thermique et catalytique
A process for the desulfurization of a fluid catalytically cracked naphtha wherein the valuable olefins are retained and recombinant mercaptans are prevented from forming, resulting in a low sulfur naphtha. Embodiments disclosed herein may allow for more flexibility in varying the end point of the naphtha used in gasoline blending.
C10G 45/02 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage
63.
PROCESS TO HYDRODESULFURIZE FCC GASOLINE RESULTING IN A LOW-MERCAPTAN PRODUCT
A process for reducing the sulfur content of a hydrocarbon stream, including: feeding a hydrocarbon stream including sulfur compounds to a catalytic distillation reactor having one or more hydrodesulfurization reaction zones; feeding hydrogen to the catalytic distillation reactor; concurrently in the catalytic distillation reactor: fractionating the hydrocarbon stream into a heavy fraction and a light fraction; contacting hydrogen and the light fraction to form H2S and a light fraction of reduced sulfur content; recovering the light fraction, H2S, and hydrogen as an overheads; recovering the heavy fraction; heating the overheads to a temperature from 500 to 700oF; feeding the heated overheads and hydrogen to a high temperature low pressure reactor to form H2S and a reactor effluent of reduced mercaptan content; separating the reactor effluent, H2S, and unreacted hydrogen to form a light hydrocarbon fraction and a fraction including H2S and hydrogen; recycling a portion of the light hydrocarbon fraction to the catalytic distillation reactor.
C10G 11/18 - Craquage catalytique, en l'absence d'hydrogène, des huiles d'hydrocarbures avec catalyseurs solides mobiles préchauffés selon la technique du "lit fluidisé"
C10G 55/06 - Traitement des huiles d'hydrocarbures, en l'absence d'hydrogène, par au moins un procédé de raffinage et par au moins un procédé de craquage uniquement par plusieurs étapes en série comprenant au moins une étape de craquage catalytique
An integrated process for treating pyrolysis gasolines, including: feeding the pyrolysis gasoline to a first stage wherein the pyrolysis gasoline is substantially depentanized and acetylene and diolefins are reacted with hydrogen to produce an effluent having a reduced acetylene and diolefin content; and feeding the effluent to a second stage, wherein the second stage comprises a catalytic distillation hydrotreating process. The second stage may include a first catalytic distillation reactor system comprising a first distillation reaction zone containing a first hydrogenation catalyst, and the process may further include treating a C6-boiling material in the first distillation reaction zone to react sulfur compounds with hydrogen to produce hydrogen sulfide, the treated C6 material being concurrently separated as a second overheads from C7 and heavier material by fractional distillation, the C7 and heavier material being removed from the first distillation reaction zone as a first bottoms.
C10G 65/12 - Traitement des huiles d'hydrocarbures, uniquement par plusieurs procédés d'hydrotraitement uniquement par plusieurs étapes en série comprenant des étapes de craquage et d'autres étapes d'hydrotraitement
C10G 45/04 - Raffinage des huiles d'hydrocarbures au moyen d'hydrogène ou de composés donneurs d'hydrogène pour éliminer des hétéro-atomes sans modifier le squelette de l'hydrocarbure mis en œuvre et sans craquage en hydrocarbures à point d'ébullition inférieurHydrofinissage caractérisé par le catalyseur utilisé
A process for the production of olefins from at least one of an alcohol and ether, the process including: contacting at least one alcohol or ether with a hydrofluoric acid-treated amorphous synthetic alumina-silica catalyst under decomposition conditions to produce an olefin. Also disclosed is a process for the production of isobutylene from methyl tertiary butyl ether, the process including: feeding methyl tertiary butyl ether (MTBE) to a reactor having at least one reaction zone containing a hydrofluoric acid-treated amorphous synthetic alumina-silica catalyst; contacting the MTBE with the hydrofluoric acid-treated amorphous synthetic alumina-silica catalyst under decomposition conditions to produce a reactor effluent comprising isobutylene, unreacted MTBE, heavies, and methanol; feeding the reactor effluent to a first distillation column; separating the isobutylene from the unreacted MTBE, heavies, and the methanol in the first distillation column to recover a first bottoms fraction comprising heavies, unreacted MTBE, and methanol and an isobutylene-rich overheads fraction.
C07C 1/20 - Préparation d'hydrocarbures à partir d'un ou plusieurs composés, aucun d'eux n'étant un hydrocarbure à partir de composés organiques ne renfermant que des atomes d'oxygène en tant qu'hétéro-atomes
A process for the oligomerization of propylene is disclosed wherein a tungstated zirconia catalyst prepared as a distillation structure is used in a reaction distillation zone under conditions of temperature and pressure to concurrently react the propylene to produce oligomers thereof and separate the oligomer products from unreacted propylene by fractional distillation in a distillation column reactor. Compared to the prior art tubular or plug flow reactors, lower temperatures and pressures are used to produce higher conversions and selectivities to preferred isomeric forms useful for preparing neo acids.
C10G 50/00 - Production de mélanges d'hydrocarbures liquides à partir d'hydrocarbures à nombre inférieur d'atomes de carbone, p. ex. par oligomérisation
C10G 51/04 - Traitement des huiles d'hydrocarbures, en l'absence d'hydrogène, uniquement par plusieurs procédés de craquage uniquement par plusieurs étapes en série ne comprenant que des étapes de craquage thermique et catalytique
C10G 11/02 - Craquage catalytique, en l'absence d'hydrogène, des huiles d'hydrocarbures caractérisé par le catalyseur utilisé
B01J 21/06 - Silicium, titane, zirconium ou hafniumLeurs oxydes ou hydroxydes
A process for the production of olefins from at least one of an alcohol and ether, the process including: contacting at least one alcohol or ether with a hydrofluoric acid-treated amorphous synthetic alumina-silica catalyst under decomposition conditions to produce an olefin. Also disclosed is a process for the production of isobutylene from methyl tertiary butyl ether, the process including: feeding methyl tertiary butyl ether (MTBE) to a reactor having at least one reaction zone containing a hydrofluoric acid-treated amorphous synthetic alumina-silica catalyst; contacting the MTBE with the hydrofluoric acid-treated amorphous synthetic alumina-silica catalyst under decomposition conditions to produce a reactor effluent comprising isobutylene, unreacted MTBE, heavies, and methanol; feeding the reactor effluent to a first distillation column; separating the isobutylene from the unreacted MTBE, heavies, and the methanol in the first distillation column to recover a first bottoms fraction comprising heavies, unreacted MTBE, and methanol and an isobutylene-rich overheads fraction.
C07C 1/20 - Préparation d'hydrocarbures à partir d'un ou plusieurs composés, aucun d'eux n'étant un hydrocarbure à partir de composés organiques ne renfermant que des atomes d'oxygène en tant qu'hétéro-atomes
A process for the oligomerization of propylene is disclosed wherein a tungstated zirconia catalyst prepared as a distillation structure is used in a reaction distillation zone under conditions of temperature and pressure to concurrently react the propylene to produce oligomers thereof and separate the oligomer products from unreacted propylene by fractional distillation in a distillation column reactor. Compared to the prior art tubular or plug flow reactors, lower temperatures and pressures are used to produce higher conversions and selectivities to preferred isomeric forms useful for preparing neo acids.
A process for the conversion of tertiary butyl alcohol to ethyl tertiary butyl ether, including: dehydrating tertiary butyl alcohol to form a product stream comprising isobutylene and water; separating the product stream to form an isobutylene-rich fraction and a water-rich fraction; separating the water-rich fraction to recover a hydrocarbon fraction and a water fraction having less than 1 ppm hydrocarbon content; reacting isobutylene in the isobutylene-rich fraction with ethanol to form a reaction product comprising ethyl tertiary butyl ether; separating the reaction product to recover unreacted ethanol and an ethyl tertiary butyl ether stream; and recycling at least a portion of the unreacted ethanol to the reacting; wherein the ethyl tertiary butyl ether stream comprises at least 99 weight percent ethyl tertiary butyl ether.
A process for the conversion of tertiary butyl alcohol to ethyl tertiary butyl ether, including: dehydrating tertiary butyl alcohol to form a product stream comprising isobutylene and water; separating the product stream to form an isobutylene-rich fraction and a water-rich fraction; separating the water-rich fraction to recover a hydrocarbon fraction and a water fraction having less than 1 ppm hydrocarbon content; reacting isobutylene in the isobutylene-rich fraction with ethanol to form a reaction product comprising ethyl tertiary butyl ether; separating the reaction product to recover unreacted ethanol and an ethyl tertiary butyl ether stream; and recycling at least a portion of the unreacted ethanol to the reacting; wherein the ethyl tertiary butyl ether stream comprises at least 99 weight percent ethyl tertiary butyl ether.
C07C 41/09 - Préparation d'éthers par déshydratation de composés contenant des groupes hydroxyle
B01J 8/02 - Procédés chimiques ou physiques en général, conduits en présence de fluides et de particules solidesAppareillage pour de tels procédés avec des particules immobiles, p. ex. dans des lits fixes
A process for the production of dialkyl ether, the process including: feeding a stream comprising an alkyl alcohol to a distillation column reactor system; concurrently in the distillation column reactor system: i) contacting the alkyl alcohol with a catalytic distillation structure in a distillation reaction zone thereby catalytically reacting at least a portion of the alkyl alcohol to form a corresponding dialkyl ether and water; and ii) fractionating the resulting dialkyl ether from the water; operating the distillation column reactor system to obtain substantially complete conversion of the alkyl alcohol to form the corresponding dialkyl ether and water; recovering the dialkyl ether from the distillation column reactor as an overheads fraction; recovering the water from the distillation column reactor as a bottoms fraction.
A process for the production of tertiary ethers, including: feeding a hydrocarbon stream comprising isoolefins and propionitrile to a distillation column reactor system containing at least one etherification reaction zone; feeding a C2 to C6 monoalcohol or mixture thereof to the distillation column reactor; concurrently in the distillation column reactor system: reacting a portion of the isoolefins with a portion of the alcohols to form a tertiary ether; and separating the tertiary ether from unreacted isoolefins; withdrawing the tertiary ether and propionitrile from the distillation column reactor system as a bottoms; withdrawing the unreacted isoolefins from the distillation column reactor system as an overheads; and operating the distillation column reactor system such that the etherification reaction zone is substantially free of propionitrile.
6 monoalcohol or mixture thereof to the distillation column reactor; concurrently in the distillation column reactor system: reacting a portion of the isoolefins with a portion of the alcohols to form a tertiary ether; and separating the tertiary ether from unreacted isoolefins; withdrawing the tertiary ether and propionitrile from the distillation column reactor system as a bottoms; withdrawing the unreacted isoolefins from the distillation column reactor system as an overheads; and operating the distillation column reactor system such that the etherification reaction zone is substantially free of propionitrile.
B01D 3/34 - Distillation ou procédés d'échange apparentés dans lesquels des liquides sont en contact avec des milieux gazeux, p. ex. extraction avec une ou plusieurs substances auxiliaires
A catalyst useful for multi-phase reactors that includes an active component surrounded by a coating on a surface of the active component, wherein the coating provides a liquid film around the active component to increase the useful life of the active component as compared to an uncoated active component.
A catalyst useful for multi-phase reactors that includes an active component surrounded by a coating on a surface of the active component, wherein the coating provides a liquid film around the active component to increase the useful life of the active component as compared to an uncoated active component.
A catalyst useful for multi-phase reactors that includes an active component surrounded by a coating on a surface of the active component, wherein the coating provides a liquid film around the active component to increase the useful life of the active component as compared to an uncoated active component.
A process for the removal of aromatic compounds from the olefin feed to a sulfuric acid paraffin alkylation by feeding a olefin containing hydrocarbon stream and a dilute alkylate stream from a paraffin alkylation to a distillation zone and removing unreacted material from said hydrocarbon stream as overheads and removing a more concentrated alkylate product stream and a portion of said aromatic compounds as bottoms and the improved alkylation process resulting therefrom.
A process for the removal of aromatic compounds from an olefin feed to a paraffin alkylation is disclosed. The process may include feeding a olefin and aromatic containing hydrocarbon stream and a dilute alkylate product stream comprising alkylate product and unreacted material from the paraffin alkylation to a distillation zone and removing the unreacted material as overheads and removing a more concentrated alkylate product stream and a portion of the aromatic compounds as bottoms resulting in an improved alkylation process.
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Produits et services
Licensing of oil refining and petrochemical technologies; Consultation services in the field of the licensing of oil refining and petrochemical technology
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Produits et services
Licensing of oil refining and petrochemical technologies; Consultation services in the field of the licensing of oil refining and petrochemical technology
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Produits et services
Licensing of oil refining and petrochemical technologies; Consultation services in the field of the licensing of oil refining and petrochemical technology
Catalytic Distillation Technologies, Chemical Research & Licensing Company, a Texas Corporation and Lummus Technology, LLC., a Delaware Limited Liability Company ()
45 - Services juridiques; services de sécurité; services personnels pour individus
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Licensing of oil refining and petrochemical technologies; Consultation services in the field of the licensing of oil refining and petrochemical technology
Catalytic Distillation Technologies, Chemical Research & Licensing Company, a Texas Corporation and Lummus Technology, Inc., a Delaware Limited Liability Company ()
45 - Services juridiques; services de sécurité; services personnels pour individus
Produits et services
Licensing of oil refining and petrochemical technologies; Consultation services in the field of the licensing of oil refining and petrochemical technology
45 - Services juridiques; services de sécurité; services personnels pour individus
Produits et services
Licensing of oil refining and petrochemical technologies; Consultation services in the field of the licensing of oil refining and petrochemical technology
Catalytic Distillation Technologies, Chemical Research & Licensing Company, a Texas Corporation and Lummus Technology, LLC, a Delaware Limited Liability Company ()
45 - Services juridiques; services de sécurité; services personnels pour individus
Produits et services
Licensing of oil refining and petrochemical technologies; Consultation services in the field of the licensing of oil refining and petrochemical technology
Catalytic Distillation Technologies, Chemical Research & Licensing Company, a Texas Corporation and Lummus Technology, Inc., a Delaware Limited Liability Company ()
45 - Services juridiques; services de sécurité; services personnels pour individus
Produits et services
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Catalytic Distillation Technologies, Chemical Research & Licensing Company, a Texas Corporation and Lummus Technology, LLC., a Delaware Limited Liability Company ()
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An integrated process for he isolation of benzene contained within a fluid catalytically cracked naphtha is disclosed wherein a C6 fraction containing a benzene concentrate is subjected to etherification with alcohol (e.g. methanol and/or ethanol) to convert the C6 isoolefins to ethers which are separated by fractional distillation. If desired the ethers may be dissociated to the isoolefins and alcohol. The remaining material in the benzene concentrate may then be treated to remove olefins and organic sulfur compounds so that the benzene may be removed by solvent extraction. Alternatively the benzene in the remaining material may be subjected to hydrogenation.
C07C 7/148 - Purification, séparation ou stabilisation d'hydrocarburesEmploi d'additifs par traitement provoquant une modification chimique d'au moins un composé
C07C 13/16 - Hydrocarbures monocycliques ou leurs dérivés hydrocarbonés acycliques à cycle hexagonal
A process for the oligomerization of propylene is disclosed wherein MCM-22 zeolite prepared as a distillation structure is used in a reaction distillation zone under conditions of temperature and pressure to concurrently react the propylene to produce oligomers thereof and separate the oligomer products from unreacted propylene by fractional distillation in a distillation column reactor. Compared to the prior art tubular or plug flow reactors, lower temperatures and pressures are used to produce higher conversions and selectivities to preferred isomeric forms.
C07C 2/02 - Préparation d'hydrocarbures à partir d'hydrocarbures contenant un plus petit nombre d'atomes de carbone par addition d'hydrocarbures non saturés entre eux
4 product is then fed to the second alkylation system to provide the isobutane. The effluent from the second alkylation system is fed to a traditional deisobutanizer to prevent any build up of normal butanes in the system.
A process is disclosed for the preferential conversion to 2-butene of a C4 stream containing 1-butene and 2-butene. The process involves mixing the C4 stream with a first hydrogen stream to form a feed stream, hydroisomerizing the feed stream in the presence of a first hydroisomerization catalyst in order to convert at least a portion of the 1-butene to 2-butene, thereby producing a hydroisomerization effluent, separating the hydroisomerization effluent in a fractionation column having an upper end and a lower end to form a 1-butene mixture at the upper end, a top effluent stream containing isobutane and isobutylene and a bottoms stream containing 2-butene, and hydroisomerizing the 1-butene mixture at the upper end of the column using a second hydroisomerization catalyst. A corresponding apparatus also is disclosed.
CATALYTIC DISTILLATION TECHNOLOGIES, Chemical Research and Licensing Company, a Texas corporation, and Lummus Technology Inc., a Delaware corporation ()
Catalytic Distillation Technologies, composed of Chemical Research and Licensing Company, a Texas corporation, and ABB Lummus Crest, Inc., a Delaware corporation ()
Catalytic Distillation Technologies, composed of Chemical Research and Licensing Company, a Texas corporation and Lummus Crest, Inc., a Delaware corporation (USA)
Catalytic Distillation Technologies, composed of Chemical Research and Licensing Company, a Texas corporation and CB&I Technology Inc., a Delaware corporation (USA)
Catalytic Distillation Technologies, composed of Chemical Research and Licensing Company, a Texas corporation and Lummus Crest, Inc., a Delaware corporation (USA)
Catalytic Distillation Technologies, composed of Chemical Research and Licensing Company, a Texas corporation and ABB Lummus Crest, Inc., a Delaware corporation ()
Catalytic Distillation Technologies, composed of Chemical Research and Licensing Company, a Texas corporation, and Lummus Technology Inc., a Delaware corporation ()
