Patent classifications
C10G2300/1051
Halogen-free ionic liquids in naphtha desulfurization and their recovery
Ionic liquids of the general formula C.sup.+A.sup.− where C.sup.+ represents an organic cation, specifically, but not limited to the imidazolium, pyridinium, isoquinolinium, ammonium types, which have aliphatic and aromatic substituents, while A.sup.− represents a carboxylate, aromatic and aliphatic anion. The ionic liquids are synthesized under conventional heating or microwave irradiation This invention is also related to the application of ionic liquids to remove sulfur compounds of naphthas through a liquid-liquid extraction and the recovery and reuse of ionic liquids by the application of heat, reduced pressure and washing with solvents.
Method for producing olefins and monocyclic aromatic hydrocarbons by a combination of steam cracking, dicyclopentadiene reduction, and cracking and reforming
A method for producing an olefin and a monocyclic aromatic hydrocarbon of the present invention includes a dicyclopentadiene removal treatment step of removing dicyclopentadienes having a dicyclopentadiene skeleton from a feedstock oil which is a thermally-cracked heavy oil obtained from an apparatus for producing ethylene and which has a 90 volume % distillate temperature, as a distillation characteristic, of 390° C. or lower; and a cracking and reforming reaction step of obtaining a product containing an olefin and a monocyclic aromatic hydrocarbon by bringing the feedstock oil having a content of dicyclopentadienes adjusted to 10% by weight or less by treating a part or all of the feedstock oil through the dicyclopentadiene removal step into contact with a catalyst and reacting the feedstock oil.
Processes for the preparation of an olefinic product
The invention provides a process for the preparation of an olefinic product, comprising: (a) reacting an oxygenate feedstock, in a reaction zone in the presence of a molecular sieve catalyst, at a temperature from 350 to 1000° C., to produce a reaction effluent stream, comprising at least oxygenate, olefin, water and acidic by-products; (b) cooling the reaction effluent stream by means of an indirect heat exchange to a temperature greater than the dew point temperature of reaction effluent stream; (c) further rapidly cooling the reaction effluent stream to a temperature lower than the dew point temperature of the reaction effluent stream by direct injection of an aqueous liquid into the reaction effluent stream, to form a first quench effluent stream; and (d) separating the first quench effluent stream into a first liquid quench effluent stream and a first gaseous quench effluent stream, comprising the olefinic product.
HEAVY AMINES AS HYDROGEN SULFIDE AND MERCAPTAN SCAVENGERS
The present invention generally relates to compositions and methods for scavenging hydrogen sulfide and/or mercaptans from fluids. More particularly, the invention relates to the use of compositions comprising a surfactant and the reaction product between a polyamine and a formaldehyde as a hydrogen sulfide or a mercaptan scavenger for hydrocarbon-containing fluids, particularly for natural gas, crude oil, field oil, fuel oil, naphtha, gasoline, kerosene, diesel, slurry oil, gas oil, resid, refinery gas, coal gas, tar, asphalt, coke gas, ammonia synthesis gas, gas from an industrial gas stream, or a sulfurization plant.
Conversion of MEROX process by-products to useful products in an integrated refinery process
An integrated refinery process for removing mercaptans from a hydrocarbon stream containing mercaptans and converting by-product disulfide oil to useful products. The process includes introducing the hydrocarbon stream containing mercaptans into an extraction vessel containing an alkaline solution and passing the hydrocarbon stream through an extraction section of the extraction vessel which includes one or more liquid-liquid contacting decks for reaction to convert the mercaptans to alkali metal alkanethiolates. Further, the process includes withdrawing a hydrocarbon product stream free of mercaptans from the extraction vessel and recovering spent caustic containing alkali metal alkanethiolates from the extraction vessel. Additionally, the process includes subjecting the spent caustic containing alkali metal alkanethiolates to air oxidation to produce a by-product stream containing disulfide oils (DSO) and sulfides and processing the by-product stream in a steam cracking unit to produce a DSO free product stream.
Process for the Production of High Value Chemicals from Biologically Produced Materials
The present invention relates to a process for the production of high value chemicals, preferably including at least ethylene and propylene, by steam cracking a mixture of non-cyclic paraffin stream (A) comprising at least 90% of components having at least 12 carbon atoms, with either a mixture of hydrocarbons having from 3 to 4 carbon atoms or a mixture of hydrocarbons comprising at least 90% of components having a boiling point ranging from 15° C. to 200° C.
Desulfurization and sulfur tolerant hydrogenation processes of hydrocarbon feedstocks
The present invention relates to the use of adsorbents comprising zinc oxide nanowires decorated with catalytically active metal particles for the removal of sulfur from hydrocarbon feedstocks, including the desulfurization of diesel fuels and the deep desulfurization of natural gas, and to the use of decorated zinc oxide nanowire adsorbents for the hydrogenation of naphthalene selectively to tetralin in the presence of sulfur compounds. The adsorbent comprises nickel metal particles or nickel-zinc alloy particles deposited on zinc oxide nanowires.
ADDITIONAL HEAT SOURCE FOR NAPHTHA CATALYTIC CRACKING
Systems and methods for producing olefins and/or aromatics via catalytically cracking a hydrocarbon feed are disclosed. The hydrocarbon feed is cracked in a reaction unit having one or more fluidized bed reactors. The catalyst particles are then separated from at least some of the gas product in a solid-gas separation unit to form separated catalyst particles. Methane is injected into the catalyst regeneration unit. The methane is burnt in the regeneration unit to provide additional heat to the regenerated catalyst such that the regenerated catalyst particles are at a temperature sufficient for the cracking when the regenerated catalyst particles are flowed to the reaction unit.
PROCESS FOR MODIFYING A HETEROGENEOUS CATALYST WITH AN ORGANOMETALLIC COMPOUND, A HETEROGENEOUS CATALYST AND SYSTEM THEREOF
The present disclosure relates to a process and system for modifying heterogeneous catalysts by contacting them with chemical compounds. Specifically, the present disclosure relates to an easy and convenient process for surface functionalizing of a heterogeneous catalyst such as polymetallic catalyst including bimetallic catalyst by employing precursor of inorganic compound, wherein the precursor is organometallic compound and wherein the inorganic compound includes but is not limited to a metal based inorganic compound such as aluminium oxide. The present disclosure thus provides for easy and convenient process and system for surface modification/functionalization of heterogeneous catalysts by employing precursor of inorganic compound at conditions including but not limiting to room temperature and atmospheric pressure.
Catalyst for producing monocyclic aromatic hydrocarbons, and method for producing monocyclic aromatic hydrocarbons
A catalyst for producing monocyclic aromatic hydrocarbons, used for producing monocyclic aromatic hydrocarbons of 6 to 8 carbon number from a feedstock oil having a 10 volume % distillation temperature of at least 140° C. and an end point temperature of not more than 400° C., wherein the catalyst contains a crystalline aluminosilicate, gallium and/or zinc, and phosphorus, the molar ratio between silicon and aluminum (Si/Al ratio) in the crystalline aluminosilicate is not more than 100, the molar ratio between the phosphorus supported on the crystalline aluminosilicate and the aluminum of the crystalline aluminosilicate (P/Al ratio) is not less than 0.01 and not more than 1.0, and the amount of gallium and/or zinc is not more than 1.2% by mass based on the mass of the crystalline aluminosilicate.