Abstract: Reverse flow reactor (RFR) apparatuses exhibiting asymmetric feed profiles and improved purge mode efficiency, and methods of using same to transform a hydrocarbon feed into a pyrolysed hydrocarbon product are disclosed. The RFR apparatus includes an RFR body with a reaction zone having at least one bed. The RFR body has a central vertical axis and flanked by first and second void spaces. The method utilizes at least two oxygen-containing feeds, a combustion fuel feed, a purge feed, and a hydrocarbon pyrolysis feed. The RFR apparatus can cycle between an exothermic heating mode (heated to ?700° C.

Abstract: An apparatus and method are provided for processing hydrocarbon feeds. The method enhances the conversion of hydrocarbon feeds into conversion products, such as ethylene and propylene. In particular, the present techniques utilize a high-severity reactor integrated with another reactor type to convert hydrocarbons to other petrochemical products.

Abstract: A process is presented for the dehydrogenation of hydrocarbons in a radial flow reactor. The process includes the continuous feeding of catalyst into the reactor and the continuous withdrawal of catalyst from the reactor, where the catalyst is modified to increase the increased density. The catalyst is a layered structure with a dense core and an active catalytic outer layer.

Abstract: A processing scheme and arrangement for enhanced olefin production involves cooling or treating an olefin cracking reactor effluent stream by contacting the olefin cracking reactor effluent stream with a quench oil stream in a single contact cooler contact zone to produce a cooled vapor stream and to form a heated quench oil stream. A pressure differential across the single contact cooler is less than about 3.5 kPa. The heated quench oil stream can be subsequently cooled and returned to the single contact cooler.

Abstract: The conversion of a charge comprising at least one oxygen compound is performed in a reactor C, into which the charge is introduced by the pipe (11), the solid catalytic particles forming the dense phase D1 by the pipe (14) and the solid entrainment gas by the pipe (12). The reactor is connected by a pipe (1) to a cocurrent cyclone separator-mixer (MS) making it possible to separate a solid phase from a gaseous phase containing the conversion products recovered by the pipe (4'), while carrying out a quenching of said gaseous phase by a product M2 introduced by the pipe (3). The phase D1 is fed by the pipe (7) to a regenerator R before being returned by the pipe (13) into the reactor C. The mixture of the gaseous phase and the product M2 is separated in a separator and the product M2, optionally after cooling, is recycled to the mixer-separator (MS).

Abstract: Process for the production of synthesis gas and higher hydrocarbons in which a saturated hydrocarbon and an oxygen containing gas having a ratio of hydrocarbon to oxygen of greater than the stoichiometric ratio for complete combustion are introduced into a bed of an inert particulate material. The upward flow rate of the hydrocarbon/oxygen containing gas stream is sufficient to fluidize or to produce a spouting action of the bed material, whereby the particulate material is thrown up above the bed surface and subsequently falls back into the bed. The hydrocarbon and oxygen containing gas are ignited reacted together, and the products of the reaction withdrawn.

Abstract: A method for converting a lower molecular weight alkane to synthesis gas to higher molecular weight materials comprising (a) passing a reaction mixture comprising the alkane and air at a pressure of from about 1 to about 50 pounds per square inch gauge through an elongated first reactor packed with a bed of refractory particles having three zones: (1) an upstream zone for heating the mixture, (2) a middle zone wherein alkane and oxygen react exothermically to produce hot CO, H.sub.2, and N.sub.2 and (3) a downstream zone for cooling the hot CO, H.sub.2, and N.sub.2 ; and (b) passing cooled CO, H.sub.2, and N.sub.2 to a reactor packed with Fischer-Tropsch catalyst to form higher molecular weight materials.

Abstract: A process for cracking lignin-containing feed materials, such as precipitated from black liquor, to produce hydrocarbon products such as ethylene, utilizing dual fluidized beds of particulate solids in series flow arrangement. In the process, the feedstock is introduced with a diluent gas such as steam into the first or fast fluidized bed for cracking reactions at superficial gas velocity exceeding about 5 ft/sec. A particulate solids carrier material, which can comprise at least partly coke produced in the process, is circulated between the beds, and coke deposited on the carrier in the first or cracking bed at 1000.degree.-1600.degree. F. temperature is burned off in a second or combustion bed maintained at 1400.degree.-2000.degree. F. temperature by an oxygen-containing gas and diluent steam introduced therein. Superficial upward gas velocity in the fast fluidized bed zone exceeds about 5 ft/sec. and the bed density exceeds about 3 lb/cu.ft.

Abstract: A thermal cracking process and apparatus are disclosed for economical manufacture of lower olefins and valuable coproducts by pyrolysis of liquid or gaseous hydrocarbon feedstocks ranging from ethane to tar sands, particularly feedstocks, such as gas oil, naphtha, residual oils or tar sands. The pyrolysis unit is a riser reactor heated by hot agglomerated ash particles and designed for short residence time to minimize the time of contact of the feedstock with the hot ash. The agglomerated ash is continually produced in a fluidized bed combustion unit by burning particles of coal or other solid carbonaceous material, and the hot agglomerated ash is continually forced upwardly through the riser by superheated steam which is further superheated in the riser reactor and which serves as dilution steam for hydrocarbon partial pressure reduction. Additional dilution steam enters the reactor with the preheated feedstock.