Abstract: A process for increasing the yield of C3 and C4 olefins by injecting light cat naphtha and cat cycle oil together with steam into an upstream reaction zone of a FCC riser reactor. The products of the upstream reaction zone are conducted to a downstream reaction zone and combined with fresh feed in the downstream reaction zone.

Abstract: A C4+naphtha hydrocarbon feed is converted to light olefins and aromatics, by contacting the feed with a catalyst containing ZSM-5 and/or ZSM-11, a substantially inert matrix material such as silica and/or clay, having less than about 20 wt % active matrix material based on total catalyst composition, and phosphorus.

Abstract: The invention is related to a two step process wherein the first step comprises cracking an olefinic naphtha resulting in a cracked product having a diminished total concentration of olefinic species. The second step comprises hydroprocessing at least a portion of the cracked product, especially a naphtha fraction, to provide a hydroprocessed cracked product having a reduced concentration of contaminant species but without a substantial octane reduction.

Abstract: A process for producing propylene from a catalytically cracked or thermally cracked naphtha stream is disclosed herein. The naphtha stream is contacted with a catalyst containing from about 10 to 50 wt. % of a crystalline zeolite having an average pore diameter less than about 0.7 nanometers at reaction conditions which include temperatures from about 500° C. to 650° C. and a hydrocarbon partial pressure from about 10 to 40 psia. A separate stream containing aromatics may be co-fed with the naphtha stream.

Abstract: Olefins may be produced by thermally steam cracking residuum containing a short residuum having a boiling point range greater than 565° C. wherein at least 3 weight percent of the short residuum has a boiling point greater than or equal to 650° C. The residuum has pentane insolubles less than or equal to 1.2, ASTM 893. Further, the weight percent of hydrogen of the residuum is greater than or equal to 12.5. Such feedstocks are produced by hydrotreating, where necessary, a petroleum residuum having pentane insolubles less than 1.0, ASTM 893, until the weight percent of hydrogen of the petroleum residuum is 12.5. Where necessary, the petroleum residuum may be deasphalted prior to subjecting it to hydrotreatment.

Abstract: Disclosed are silicoaluminates (SAPOs) having unique silicon distributions, a method for their preparation and their use as naphtha cracking catalysts. More particularly, the new SAPOs have a high silica:alumina ratio and favorable Si atom distribution.

Abstract: Olefins may be produced by thermally steam cracking a crude oil having pentane insolubles less than or equal to 1.2, ASTM D-893, and a weight percent of hydrogen greater than or equal to 12.5.

Abstract: A method and apparatus for decoking and suppressing coke formation during pyrolysis has been discovered that does not require complete shut down of the pyrolysis furnace. For the decoking step, the hydrocarbon feed is cut off to one or more coils for usually less than about three hours during which a decoking additive is added to the steam flow in that coil. This additive is comprised of an aqueous solution of a group IA metal salt and a group IIA metal salt and catalyzes the coke removal. The hydrocarbon feed continues in the other coils during this procedure. After decoking, a suppression additive also comprising group IA and IIA metals is added to the steam and hydrocarbon feed. This suppression additive will melt onto the inner surfaces of the pyrolysis furnace coils, coating the coils with a glass layer which inhibits coke formation.

Abstract: A hydrocarbon feed containing C4-C7 olefins and/or paraffins is converted to light olefins, by contacting the feed with a catalyst containing ZSM-5 and/or ZSM-11, having an initial silica to alumina ratio greater than about 300:1, and phosphorus.

Abstract: An integrated process for converting a hydrocarbon feedstock having components boiling above about 100° C. into steam cracked products is described. The process first involves passing the feedstock to a hydrotreating zone at a pressure in the range of from about 400 psig to about 1,250 psig to effect substantially complete decomposition of organic sulfur and/or nitrogen compounds. The product from the hydrotreating zone is passed to a steam cracking zone. Hydrogen and C1-C4 hydrocarbons, steam cracked naphtha, steam cracked gas oil and steam cracked tar are recovered, where the amount of steam cracked tar produced is reduced by at least about 15 percent, basis the starting hydrocarbon feedstock which has not been subject to hydrotreating.

Abstract: A process for selectively producing C.sub.2 -C.sub.4 olefins from a catalytically cracked or thermally cracked naphtha stream. The naphtha stream is contacted with a catalyst containing from about 10 to 50 wt. % of a crystalline zeolite having an average pore diameter less than about 0.7 nanometers at reaction conditions which include temperatures from about 500 to 650.degree. C. and a hydrocarbon partial pressure from about 10 to 40 psia.

Abstract: Sulphur-containing hydrocarbon feedstocks are desulphurized prior to being subjected to steam cracking in the presence of one or more thiohydrocarbons wherein the sulphur is part of aromatic heterocycles, preferably thiophene and/or benzothiophene. Optimum results are obtained in terms of the combination of reduced coking rate and reduced carbon monoxide formation.

Abstract: A process to convert propane into ethylene, propene, and C.sub.4 olefins, is provided. This process comprises: contacting propane with a composition under converting conditions.

Abstract: A feed mixture containing C.sub.4 -olefins to C.sub.7 -olefins is evaporated and mixed with steam in a weight ratio of H.sub.2 O:hydrocarbons in the range from 0.5:1 to 3:1. The steam containing feed mixture with an inlet temperature in the range from 380.degree. to 500.degree. C. is introduced into a reactor, which contains a bed of granular, form-selective zeolite catalyst. The zeolite is of the pentasil type and has an atomic ratio of Si:Al of 10:1 to 200:1. From the bed a product mixture is withdrawn whose temperature is 20.degree. to 80.degree. lower than the inlet temperature, and whose total content of propylene and butene isomers is at least 60 wt-% of the olefinic constituents of the feed mixture.

Abstract: A continuous pyrolysis and decoking process and apparatus is described for the production of acetylenic compounds, in which hydrocarbons and steam are circulated in at least one tube (31) of a steam cracking reactor (30) and steam is circulated in at least one tube (32) of that reactor. The hydrocarbon effluent and steam then circulate in at least one row (1) of a pyrolysis reactor (40) and the decoking effluent comprising steam circulate in at least one other row (2) of that reactor (4) to effect decoking. A set of valves V1, V2, V11, V12 is used to alternate the pyrolysis step path and the decoking step path. The temperature in the steam cracking furnaces is lower than that in the pyrolysis reactor.

Abstract: A tertiary butyl alcohol feedstock is dehydrated to form isobutylene and water in a reactive distillation column having a reactive distillation section in the middle portion thereof containing a bed of a TBA dehydration catalyst and a substantially anhydrous lower boiling isobutylene fraction is recovered adjacent the top of the reactive distillation column and a higher boiling aqueous fraction is recovered adjacent the bottom of the reactive distillation column.

Abstract: The invention includes a method for skeletal isomerization of C.sub.4-5 olefins. The method includes contacting in a FCC zone, at FCC conditions, an n-C.sub.4-5 olefins-containing etherification zone raffinate, with an FCC catalyst, where at least a portion of the n-C.sub.4-5 olefins in the n-C.sub.4-5 olefins-containing etherification zone raffinate are converted to iso-C.sub.4-5 olefins.

Abstract: An alkene skeletal isomerization process is employed in an integrated process for the production of tertiary ether, e.g., tertiary amyl methyl ether (TAME) from the reaction of isoamylenes (iC.sub.5.sup.= 's) with methanol in the presence of an acid cation exchange resin. A light naphtha from a fluid catalytic cracking unit is used as the source of the iC.sub.5.sup.= 's in a process which separates the C.sub.5 containing fraction from the light naphtha, selectively hydrogenates the di-olefins contained in the C.sub.5 containing fraction, reacts the iC.sub.5.sup.= 's contained in the C.sub.5 containing fraction with methanol to form TAME, separates the TAME from the unreacted materials as a product, separates methanol from the unreacted materials, isomerizes a portion of the nC.sub.5.sup.= 's to iC.sub.5.sup.= 's , for example using a zeolite or an alumina treated with methanol, and use of the isomerization product as feed for a TAME reactor.

Abstract: A thermal cracking process is provided which comprises contacting a thermal cracking furnace with a fluid stream which comprises steam and a polysulfide such as di-t-nonylpolysulfide under a condition sufficient to effect the suppression of the formation of carbon monoxide and thereafter introducing a steam fluid containing a saturated hydrocarbon such as ethane and a polysulfide such as di-t-nonylpolysulfide under a condition sufficient to convert the saturated hydrocarbon to an olefinic compound such as ethylene.

Abstract: Steam-free non-catalytic cracking of hydrocarbons in reaction zomes each having surfaces heated externally and a heated surface to volume ratio above 3 cm-.sup.1, at a rate such that the flow through each reaction zone is essentially laminar.

Abstract: An improved method of thermally cracking hydrocarbons to produce olefin wherein a gaseous stream containing hydrocarbons is passed through a heated metal tube in a pyrolysis furnace, the improvement comprising enhancing the olefin yield by exposing the gaseous stream to a barium silicate glass-ceramic as the gaseous stream passes through the tube.

Abstract: A process for the production of olefins in an olefin plant, which includes an olefin pyrolysis furnace having pyrolysis tubes in which hydrocarbon feedstock is cracked, comprises introducing hydrocarbon feed substantially free of phosphorous-containing compounds into the pyrolysis furnace and operating the furnace under pyrolysis conditions producing olefin-containing effluent therefrom wherein the pyrolysis tubes have an effective passivator of metal catalytic sites bonded to the exposed metal surface by injecting an effective passivator into the furnace at a point above the dew point of water.

Abstract: A process for the thermal pyrolysis of hydrocarbons in a reactor (1) of elongate shape comprising at a first end supply means (5) for a gaseous mixture containing at least one hydrocarbon, at the opposite end discharge means (10) for the effluents produced and between these two ends supply means (9) for effluent cooling fluid, the reactor comprising in a first part (first end side) a plurality of electric heating means (3) enclosed by casings (4) disposed in substantially mutually parallel layers perpendicular to the axis of the reactor, in such a way as to define between the casings and/or the casings and the walls (22), spaces or passages for circulation of the gaseous mixtures and/or effluents. The heating means heat the passages in successive, individual, transverse sections which are substantially perpendicular to the axis of the reactor. The reactor comprises means for introducing into the casings (4) a gas G known as a casing gas which preferably contains water vapour and/or hydrogen.

Abstract: A composite fluid catalytic cracking catalyst comprising a non-zeolitic component of at least 45% Al.sub.2 O.sub.3 and containing .ltoreq.30% Y zeolite with unit cell size .ltoreq.24.29 .ANG., the matrix (non-zeolitic component) of said catalyst having a B.E.T. surface area .gtoreq.50 m.sup.2 /g and a catalyst Lewis/Bronsted acid site ratio of .gtoreq.1.5 wherein the total number of Bronsted acid sites is .ltoreq.30 micromoles/g of catalyst. The catalyst is used to increase the isobutylene and isoamylenes content of cracked products obtained in a fluid catalytic cracking unit.

Abstract: Olefins are converted to lower alkene hydrocarbon products, e.g., propene, butenes, and isoalkenes with zeolite MCM-22 catalyst. This catalytic conversion is particularly useful in the selective separation of linear olefins in mixed hydrocarbon streams, employing MCM-22 catalyst to convert these straight-chain unsaturated components to lighter products, particularly, C.sub.3 -C.sub.4 olefins. One potential application of this selective separation is in the removal of linear olefins from FCC gasoline.

Abstract: A paraffin having 5 to 10 carbon atoms is catalytically cracked in the presence of a catalytically cracking catalyst having a strong acidity, especially a rare earth metal ion-exchanged mordenite or a dealuminized mordenite, to form a paraffin having 3 or 4 carbon atoms. The formed paraffin is contacted with a dehydrogenation catalyst to obtain an olefin having 3 or 4 carbon atoms.

Abstract: A method for upgrading paraffinic naphtha to high octane fuel by contacting a feedstock, such as C7-C22 fresh virgin naphtha, with porous acid cracking catalyst under low pressure selective cracking conditions effective to produce C4 -C5 isoalkenes and C4-C5 isoalkanes. The preferred feedstock is straight run naphtha containing C7+ alkanes, at least 15 wt % C7+ cycloaliphatic hydrocarbons and less than 20% aromatics, which can be converted with a fluidized zeolite catalyst in a vertical riser reactor during a short contact period.The isoalkane products of cracking are dehydrogenated and etherified to provide high octane fuel components.

Abstract: Light olefins are converted to isoalkene-rich hydrocarbon products, e.g., isobutene and isoamylenes with zeolite MCM-22 catalyst.

Abstract: The present invention provides a method and an apparatus for pyrolytically cracking a hydrocarbon vapor feedstock. The hydrocarbon vapor feedstock is contacted with water prior to cracking. While the hydrocarbon vapor feedstock is being contacted with water, both the feedstock and the water are heated by indirect heat exchange with at least one process stream containing waste heat. Consequently, a portion of the water vaporizes and combines with the hydrocarbon vapor feedstock. The hydrocarbon vapor feedstock is subsequently cracked in the presence of the vaporized water.

Abstract: Process and apparatus for upgrading paraffinic naphtha to high octane fuel by contacting a fresh virgin naphtha feedstock stream medium pore acid cracking catalyst comprising MCM-22 zeolite under low pressure selective cracking conditions effective to produce increased yield of total C4-C5 branched aliphatic hydrocarbhons. The preferred feedstock is straight run naptha containing C7+ alkanes, at least 15 wt % C7+ cycloaliphatic hydrocarbons and less than 20% aromatics, which can be converted with a fluidized bed catalyst in a vertical riser reactor during a short contact period.The isoalkene products of cracking are etherified to provide high octane fuel components.

Abstract: Process and apparatus for upgrading paraffinic naphtha to high octane fuel by contacting a fresh virgin naphtha feedstock stream medium pore acid cracking catalyst under low pressure selective cracking conditions effective to produce at least 10 wt % C4-C5 isoalkene to obtain a light olefinic fraction rich in C4-C5 isoalkene and a C6+ liquid fraction of enhanced octane value. The preferred feedstock is straight run naphtha containing C7+ alkanes, at least 15 wt % C7+ cycloaliphatic hydrocarbons and less than 20% aromatics, which can be converted with a fluidized bed catalyst in a vertical riser reactor during a short contact period.The isoalkene products of cracking are etherified to provide high octane fuel components.

Abstract: Improved operation of the ACR process is achieved by regulating the reactions within a small area in the combustion feedstock mixing zone, "Scorch Zone", by the addition of steam or other fluid such as ethane at the point of feed injection.

Abstract: Gum and sediment formation in liquid hydrocarbon mediums are inhibited by adding to the medium an alkyl 1,2-dihydroquinoline compound, dimer, trimer or polymer thereof. The invention is particularly well-suited for use in hydrodesulfurizer processes wherein the hydrocarbon medium is typically a naphtha, diesel, kerosene, light gas and or residual fuel charge and the charge or medium is subjected to high temperature and pressure treatment in the presence of a catalyst.

Abstract: Dilution steam for steam cracking hydrocarbons to produce lower olefins is economically provided by saturating gaseous hydrocarbon feed with water at a temperature selected to achieve the particular steam to hydrocarbon ratio desired in the steam cracking step. Complete saturation of the feed gas is ensured by injecting the gas into the flooded portion of an indirectly heated tubular saturation zone.

Abstract: There is provided a process for converting propane to ethylene over a zeolite catalyst comprising ZSM-50. This zeolite may be contacted with an anhydrous acidic oxide gas capable of accepting hydrogen by reacting therewith, such as sulfur dioxide (SO.sub.2), in order to enhance the ethylene selectivity of the conversion. The zeolite may either be pretreated with this acidic oxide gas or contacted in situ by cofeeding the acidic oxide gas along with the propane reactant. Particularly in view of the tendency of zeolites such as ZSM-5 to further convert olefins produced into aromatics and other hydrocarbons, the large degree of ethylene selectivity achieved by the process of the present invention is surprising.

Abstract: A process is disclosed for converting a gaseous or vaporized hydrocarbon feedstock to a product comprising ethylene, acetylene or a mixture thereof.

Abstract: This invention relates to a method for on-line decoking of flame-cracking reactors whereby decoking is achieved without interruption of the normal operation of such reactors and without the necessity to change feed equipment and/or disassemble reactor components. While maintaining the temperature of the effluent at 1000.degree. C. to 2000.degree. C., the flow of the hydrocarbon feedstock in the reactor is periodically stopped for a time sufficient to reduce the carbon deposits to an acceptable level.

Abstract: The invention relates to a process for operation of a plant for the cracking of hydrocarbons. In this process, the hydrocarbons in the cracking furnaces are indirectly heated by the heat incurred in the combustion of a heating medium with an oxygen containing gas. In order to reduce operating costs of such a process, it is suggested to mix the waste gas of a gas turbine with air and to pass the gas mixture to the cacking furnace for combustion of the heating medium whereby an electric generator is powered by the gas turbine.

Abstract: Methods for inhibiting coke formation in pyrolytic reactors and furnaces are disclosed wherein effective alkaline earth metal salt coke retardant treatments are used. Exemplary coke retardant treatments include magnesium and calcium salts such as the acetate, chloride, and nitrate, and magnesium sulfate salt.

Abstract: A method for the selective gas-phase equilibration of at least one C.sub.3 or greater monoalkene over a HAMS-1B crystalline borosilicate-based catalyst composition employing operating conditions in which the total butylene and t-amylene C.sub.5 and lower fraction of the product are maximized and the formation of C.sub.1 to C.sub.3 hydrocarbons, total aromatics and total paraffins are minimized. In another aspect of the invention the equilibration product is usefully separated by converting the isobutylene and t-amylene fractions to their methyl ethers by reaction with methanol.

Abstract: The present invention relates to a process for the preparation of olefins and diolefins by the cracking of hydrocarbons in the presence of steam, consisting in passing a mixture of hydrocarbons and steam flowing in a cracking tube disposed inside a radiation zone of a furnace. The process is characterized in that the mean dwell time of the mixture of flowing in the cracking tube between the inlet and the outlet of the radiation zone is from 300 to 1800 milliseconds, and the reaction volume is greater in the first half of the tube length than in the second one. The present invention relates also to a cracking furnace in which the ratio between the length and the mean diameter of the cracking tube is from 200 to 600, and the tube diameter decreases from the inlet to the outlet of the radiation zone.

Abstract: The present invention relates to a process for the preparation of olefins by the cracking of hydrocarbons consisting in passing a mixture of hydrocarbons and steam flowing in a cracking tube disposed inside a radiation zone of a furnace. The process is characterized in that an increase of the cracking temperature of the mixture between the inlet and the outlet of the radiation zone is associated to a non-homogeneous distribution of the thermal power of the furnace, greater at the beginning of the cracking tube than at the end, and to a reaction volume which is greater in the second half of the length tube than in the first one.The present invention relates also to a cracking furnace in which between the inlet and the outlet of the radiation zone the diameter of the cracking tube increases and the thermal power of the heating means decreases.

Abstract: A process for the selective production of petrochemical products by thermal cracking is disclosed. The process includes feeding methanol to a thermal cracking atmosphere of hydrocarbons in such a way that the ratio, as carbon atoms, of methanol and at least one starting hydrocarbon is at least 0.05:1, thermally cracking the at least one starting hydrocarbon at a cracking temperature of from 650.degree. to 1300.degree. C., and quenching the resulting reaction product.

Abstract: MTBE can be dissociated with high selectivity to isobutene and methanol over acid action exchange resin catalysts using very high LHSV, e.g. of 7 to 35 at pressure drops of 0.5 to 50 psig through the fixed bed at reaction pressure of 0.5 to 4 atmospheres and bed temperatures in a fixed bed tubular-reactor in the range of 90.degree. C. to 160.degree. C. Good conversions are obtained and undissociated MTBE and by-products of the dissociation may be recycled to a liquid phase MTBE synthesis.

Abstract: A method and apparatus for high volume distillation of impure liquid, particularly of binary mixtures of relatively low boiling organic substances and water, comprises fractionally distilling the impure liquid to form a vapor of a low boiling organic substance; compressing the vapor; passing at least a portion of the compressed vapor through a vapor composition adjustment zone wherein the organic substance may catalytically or otherwise react or merely stabilize following compression; compressing the vapor exiting the adjustment zone to form a recompressed vapor; cooling the recompressed vapor in heat transfer relation with the impure liquid whereby the vapor at least partially condenses, transferring sufficient heat to the impure liquid for evaporating the liquid and to form the aforementioned low boiling organic vapor; and collecting the condensed low boiling organic vapor.

Abstract: Pure tert.-olefins are prepared from mixtures of hydrocarbons, which contain at least one such tert.-olefin, by reaction with an alkanol to give the corresponding alkyl tert.-alkyl ethers, and subsequent cleavage of these ethers back to the corresponding pure tert.-olefins and the alkanol, and the separation of the pure tert.-olefin from the alkanol. For this, the alkanol present after the cleavage of the ether is separated from the tert.-olefin to the extent of 60 to 99% by weight by distillation, and the residual amount of alcohol in the olefin fraction is removed by adsorption from this fraction onto a synthetic ion exchanger as an absorber resin. The admixture of the alkanol to the mixture of hydrocarbons with at least one tert.-olefin is carried out partly by using the alkanol fraction arising from the separating off of the pure tert.-olefin, and partly by desorption of the alkanol from the absorber resin with the aid of the mixture of hydrocarbons containing at least 1 tert.-olefin.