253results about "Refining with metal salts" patented technology

Contacting a crude feed with one or more catalysts to produce a total product that includes the crude product is described. The crude feed has a TAN of at least 1. At least one of the catalysts includes one or more metals from Columns 6-10 of the Periodic Table and / or one or more compounds of one or more metals from Columns 6-10 of the Periodic Table. Contacting conditions are controlled contacting such that the crude product has a TAN from about 0.001 to about 0.5.

Contact of a crude feed with one or more catalysts produces a total product that includes a crude product. The crude feed may include Micro-Carbon Residue (MCR), oxygen, sulfur, or mixtures thereof. The crude product is a liquid mixture at 25° C. and 0.101 MPa. The crude product may have a MCR residue and / or oxygen content of at most 90% of the MCR residue content and / or oxygen content of the crude feed. In some instances, the crude product may have a sulfur content of about 30% to about 70% of the sulfur content of the crude feed. One or more other properties of the crude product may be changed by at least 10% relative to the respective properties of the crude feed.

Contact of a crude feed with one or more catalysts produces a total product that include a crude product. The crude feed may a total acid number of at least 0.3. The crude product is a liquid mixture at 25° C. and 0.101 MPa. The crude product may have a total acid number of at most 90% of the total acid number of the crude feed. At least one of the catalysts may include one or more Column 6 metals of the Periodic Table and one or more Column 10 metals of the Periodic Table. One or more other properties of the crude product may be changed by at least 10% relative to the respective properties of the crude feed.

An integrated refining process for the production of high quality gasoline blending components from low value components is disclosed. In addition there is disclosed a method of improving the operating efficiency of a refinery by reducing fuel gas production and simultaneously producing high quality gasoline blending components of low volatility. The processes involve the alkylation of a refinery stream containing pentane with ethylene using an ionic liquid catalyst.

An FCC catalyst which not only deactivates catalyst poison metals, such as nickel, vanadium and the like, in feedstock oils, inhibits the generation of hydrogen or coke, has excellent cracking activity and bottom oil-treating ability, and can yield a gasoline and LCO fraction in high yields, but also retains the performances on a high level over long and has an improved catalyst life; and an FCC method using the catalyst. The FCC catalyst has a compound of a bivalent metal or of bivalent and trivalent metals showing an XRD pattern of a carbonate of the bivalent metal; an inorganic oxide matrix and the compound dispersed therein; or an inorganic oxide matrix and the compound dispersed therein together with a crystalline aluminosilicate zeolite, and relates to an FCC method in which at least one of the catalysts are used in combination with an FCC catalyst obtained by evenly dispersing a crystalline aluminosilicate zeolite in an inorganic oxide matrix.

A catalyst that one or more metals from Column 5 of the Periodic Table and / or one or more compounds of one or more metals from Column 5 of the Periodic Table is described. The catalyst exhibits one or more bands in a range from 650 cm−1 to 1000 cm−1, as determined by Raman Spectroscopy. Methods of contacting a crude feed with hydrogen with the catalyst to produce a crude product with minimal hydrogen uptake are also described.

The present invention provides a high capacity adsorbent for removing sulfur from hydrocarbon streams. The adsorbent comprises a composite material containing particles of a nickel phosphide complex NixP. The adsorbent is utilized in a sulfur removal process that does not require added hydrogen, and run at relatively low temperatures ranging from about 150° C. to about 400° C. The process of this invention enables “ultra-deep” desulfurization down to levels of about 1 ppm and less.

Methods and systems for contacting a crude feed that has a total acid number (TAN) of at least 0.3 with one or more catalysts produces a total product that includes a crude product are described. The one or more catalysts may include a first catalyst and a second catalyst. The crude product is a liquid mixture at 25° C. and 0.101 MPa and the crude product has a TAN of at most 90% of the TAN of the crude feed. One or more other properties of the crude product may be changed by at least 10% relative to the respective properties of the crude feed.

Mercury is removed from crude oils, natural gas condensates and other liquid hydrocarbons by first removing colloidal mercury and solids that contain adsorbed mercury and then treating the hydrocarbons with an organic or inorganic compound containing at least one sulfur atom reactive with mercury. The sulfur compound reacts with dissolved mercury that contaminates the hydrocarbons to form mercury-containing particulates that are then removed from the hydrocarbons to produce a purified product having a reduced mercury content. Preferably, the treating agent is an organic sulfur-containing compound such as a dithiocarbamate or sulfurized isobutylene.

In methods of preparing asphalt including asphalt / elastomeric polymer compositions, it has been discovered that the emission or evolution of H2S can be reduced by adding certain H2S scavengers to the asphalt mixture, but that not every known H2S scavenger can be effective in this method. Particularly helpful H2S scavengers include inorganic metal salts. Suitable inorganic or organic metal salt H2S scavengers include, but are not necessarily limited to those where the metal of the salt is zinc, cadmium, mercury, copper, silver, nickel, platinum, iron, or magnesium, and mixtures of these salts.

A process for the conversion of paraffin hydrocarbon feed stock via skeletal isomerisation by contacting this feed with a catalyst comprised of an ionic liquid formed from an N-containing heterocyclic and / or N-containing aliphatic organic cation and an inorganic anion derived from metal halides.

Contact of a crude feed with one or more catalysts produces a total product that includes a crude product. The crude product is a liquid mixture at 25° C. and 0.101 MPa. The one or more catalysts may include a catalyst that has a median pore diameter of at least 90 Å. One or more properties of the crude product may be changed by at least 10% relative to the respective properties of the crude feed.

Methods and systems for contacting of a crude feed with one or more catalysts produces a total product that includes a crude product are described. The crude product is a liquid mixture at 25° C. and 0.101 MPa. One or more properties of the crude product may be changed by at least 10% relative to the respective properties of the crude feed. The produced crude product may include oxygen, sulfur, residue, or mixtures thereof.

A method of upgrading a heteroatom-containing hydrocarbon feed by removing heteroatom contaminants is disclosed. The method includes contacting the heteroatom-containing hydrocarbon feed with an oxidant to oxidize the heteroatoms, contacting the oxidized-heteroatom-containing hydrocarbon feed with caustic and a selectivity promoter, and removing the heteroatom contaminants from the heteroatom-containing hydrocarbon feed. The oxidant may be used in the presence of a catalyst.

This invention relates to improved methods, processes and apparatus for the removal of sulfides from a gas, liquid or solid (substance) wherein the substance is contacted with an aqueous solution. The instant invention presents methods and processes wherein at least one of H2S, SO2 and CS2 is chemically converted in an aqueous media to a salt and / or compound comprising sulfur and a cationic moiety. Said salt and / or compound comprising sulfur and a cationic moiety is herein termed a “Sulfur Salt”. After formation of the Sulfur Salt, the Sulfur Salt is converted to elemental sulfur with a bacterium capable of metabolizing sulfur. The preferred bacterium for metabolizing sulfur is a strain from the genus Thiobacillus. The most preferred strain from the genus Thiobacillus is Thiobacillus denitrificans. The instant invention prefers an aqueous operating pH of between 6.0 and 8.0, while the most preferred aqueous pH is between 6.0 and 7.0.

Methods for separating di-olefins from mono-olefins, and olefins from non-olefins such as paraffins, oxygenates and aromatics; are provided. The methods use metal salts which complex both mono-olefins and di-olefins, but which selectively complex di-olefins in the presence of mono-olefins. The metal salts are dissolved or suspended in ionic liquids, which tend to have virtually no vapor pressure. Preferred salts are Group IB salts, more preferably silver and copper salts. A preferred silver salt is silver tetrafluoroborate. A preferred copper salt is silver CuOTf. Preferred ionic liquids are those which form stable solutions, suspensions or dispersions of the metal salts, which do not dissolve unwanted non-olefins, and which do not isomerize the mono- or di-olefins. The equivalents of the metal salt can be adjusted so that di-olefins are selectively adsorbed from mixtures of mono- and di-olefins. Alternatively, both mono- and di-olefins can be adsorbed, and the mono-olefins selectively desorbed. The latter approach can be preferred when non-olefins are also to be separated. The mono- and di-olefin-containing mixture can be in the gas phase or in the liquid phase. The flow of mono- and di-olefin-containing mixture over / through the ionic liquid can be, for example, co-current, counter-current, or staged in stirred tanks, with countercurrent being preferred.

The use of a composition including a transition metal salt and at least one water-soluble aldehyde or water-soluble aldehyde precursor scavenges H2S that is present in aqueous fluids (e.g. produced water liquid streams), natural gas and in oil and mixtures thereof (e.g. mixed production streams that contain all three phases) better than either component when used alone. The resulting scavenger combination significantly increases the reaction rate and the overall scavenging efficiency, i.e. capacity over the case where each component is used alone, in the same total amount. Non-limiting examples of the metal salt include zinc or iron carboxylates, and a non-limiting example of a water-soluble aldehyde or water-soluble aldehyde precursor is ethylene glycol hemiformal.

A process for removing mercury of the present invention is characterized in that an ionic mercury-containing liquid hydrocarbon placed in a container equipped with a circulating means is effectively contacted with a sulfur compound represented by the general formula (I): M1-S-M2 (I) wherein M1 and M2 may be the same or different and are each independently a hydrogen atom, an alkali metal or an ammonium group, by introducing the sulfur compound into a suction side and / or a discharge side of the circulating means while circulating the ionic mercury-containing liquid hydrocarbon into the container through the circulating means. By the process for removing mercury of the present invention, the ionic mercury is effectively removed from the liquid hydrocarbon in simple manner.

A process to substantially reduce the sulfur content of a liquid hydrocarbon stream by contacting the hydrocarbon stream with an aqueous stream containing a mixture of one or more extraction agents selected from hypochlorites, cyanurates and alkali metal and alkaline earth metal hydroxides, optionally in the presence of a catalyst, to remove sulfur compounds.

Methods and systems for contacting a crude feed that has a total acid number (TAN) of at least 0.3 with one or more catalysts produces a total product that includes a crude product are described. The one or more catalysts may include a first catalyst and a second catalyst. The crude product is a liquid mixture at 25° C. and 0.101 MPa and the crude product has a TAN of at most 90% of the TAN of the crude feed. One or more other properties of the crude product may be changed by at least 10% relative to the respective properties of the crude feed.

Provided is a particulate sorbent composition comprising a zinc titanate support loaded with a promoter metal in a substantially reduced valence state selected from the group consisting of cobalt, nickel, iron, manganese, copper, molybdenum, tungsten, silver, tin and vanadium, or mixtures thereof , for desulfurizing a cracked gasoline or diesel fuel feed stream in a desulfurization zone by contacting said feed stream in a desulfurization zone with a particulate adsorbent composition and then subjecting the resulting low sulfur content The stream is separated from the sulfided sorbent, which is then regenerated and activated before being recycled back to the desulfurization zone.

Trace amount levels of heavy metals such as mercury in crude oil are reduced by contacting the crude oil with a sufficient amount of a reducing agent to convert at least a portion of the non-volatile mercury into a volatile form of mercury, which can be subsequently removed by any of stripping, scrubbing, adsorption, and combinations thereof. In one embodiment, at least 50% of the mercury is removed. In another embodiment, the removal rate is at least 99%. In one embodiment, the reducing agent is selected from sulfur compounds containing at least one sulfur atom having an oxidation state less than +6; ferrous compounds; stannous compounds; oxalates; cuprous compounds; organic acids which decompose to form CO2 and / or H2 upon heating; hydroxylamine compounds; hydrazine compounds; sodium borohydride; diisobutylaluminium hydride; thiourea; transition metal halides; and mixtures thereof.

A method of desulfurizing / refining a hydrocarbon oil by which sulfur compounds are diminished to an extremely low concentration at a relatively low equipment cost and operating cost. The method of desulfurizing / refining a hydrocarbon oil comprises bringing a hydrocarbon oil containing at least one sulfur compound selected from the group consisting of thiophene compounds, benzothiophene compounds, and dibenzothiophene compounds and optionally further containing aromatic hydrocarbons into contact with a solid acid catalyst and / or an activated carbon having a transition metal oxide supported thereon to thereby desulfurize the oil. The solid acid catalyst preferably is a solid ultrastrong-acid catalyst selected among sulfuric acid radical / zirconia, sulfuric acid radical / alumina, sulfuric acid radical / tin oxide, sulfuric acid radical / iron oxide, tungstic acid / zirconia, and tungstic acid / tin oxide.

The invention is concerned with a supported or unsupported catalyst comprising an active phase constituted by a sulfur-containing group VIB element, the group VIB element being molybdenum, and a hydrodeoxygenation process with a yield of hydrodeoxygenation product which is greater than or equal to 90% of charges from renewable sources using a catalyst according to the invention.