Abstract: The present invention addresses to a process for the production of aromatic compounds from streams containing linear chains with 5 to 18 carbon atoms, of fossil or renewable origin, and application in the field of catalytic cracking aiming at a regenerator operation at much lower temperature, between 480° C. and 620° C., preferably the temperature should be between 500° C. and 600° C. The coked catalyst generated by the cracking of light streams with low potential for delta coke generation can have the combustion effected at a lower temperature. The regeneration temperature must be at least 40° C. and at most 100° C. higher than the reaction temperature, keeping the catalyst circulation high to maintain the energy balance in the reaction section. The minimum regeneration temperature can be ensured by installing an air preheating furnace before entering the regenerator and passing through the air distributor inside the regenerator. The used catalyst must contain zeolite with pores of intermediate size.

Abstract: The present invention refers to the processing of a 100% renewable load in FCC units, wherein the load comprises triglycerides of vegetable and animal source, free fatty acids, fatty acid esters, ketones, alcohols and long-chain aldehydes, using catalyst and appropriate operating conditions in order to obtain 100% renewable products with a high content of aromatic compounds, in the range of naphtha, kerosene, diesel and heavy gas oil. The product thus obtained complies with all the properties of the ASTM D1655 standard, even for contents of up to 10% renewable content. In addition, there is no need to reduce the freezing point of the fossil QAV for the introduction of the renewable component, with no impact on the yield and economy of the process.

Abstract: The present invention relates to a process for the production of bio-oil-based renewable streams for composing a diesel or aviation kerosene (AVK) pool by combining the technologies of hydroprocessing esters and fatty acids (HEFA) and thermochemical conversion of lignocellulosic biomass for generating bio-oil. The integration of conventional raw material from the HEFA pathway with a bio-oil fraction has the advantages of the use of a stream originating from the conversion of lignocellulosic material, which is widely available on the market, and also the production of a renewable stream containing aromatics in its composition.

Abstract: The present invention addresses to a hydrothermal liquefaction process capable of generating a liquid stream, rich in renewable molecules, with lower oxygen content, lower percentage of water and lower acidity compared to other products of thermochemical processes of biomass conversion. In order to effectively carry out this process, a catalyst was developed, obtained from the calcination of castor bean hull, to be used in the field of biofuels in order to provide an environmentally friendly alternative for the production of fuels.

Abstract: The present invention describes the coprocessing of a lignocellulosic liquid stream and an intermediate fossil stream in the oil refining process comprising the steps of (a) contacting said intermediate fossil stream and said lignocellulosic liquid stream with a stream of solvent of C3-C10 hydrocarbons in an extraction section, obtaining a stream of extract with solvent and a stream of raffinate with solvent; and (b) sending said stream of extract with solvent to a separation section, obtaining a deasphalted oil stream comprising solvent-free carbon of renewable origin and a stream of recovered solvent. The present invention further relates to a process for producing fuels from the deasphalted oil stream comprising carbon of renewable origin, wherein the process comprises sending the deasphalted oil stream to a conversion section of an oil refinery.

Abstract: The present invention describes the coprocessing of a lignocellulosic liquid stream and an intermediate fossil stream in the oil refining process comprising the steps of (a) contacting said intermediate fossil stream and said lignocellulosic liquid stream with a stream of solvent of C3-C10 hydrocarbons in an extraction section, obtaining a stream of extract with solvent and a stream of raffinate with solvent; and (b) sending said stream of extract with solvent to a separation section, obtaining a deasphalted oil stream comprising solvent-free carbon of renewable origin and a stream of recovered solvent. The present invention further relates to a process for producing fuels from the deasphalted oil stream comprising carbon of renewable origin, wherein the process comprises sending the deasphalted oil stream to a conversion section of an oil refinery.

Abstract: The present invention relates to a process for obtaining fuel from biomass which comprises the introduction of the catalyst (3) in the base of an cracking section (4), wherein said catalyst (3) at high temperature comes in contact with a gas stream of light hydrocarbons rich in hydrogen (1), wherein the catalyst (3) and hydrocarbon (1) then come in contact with a lignocellulosic liquid stream (2) in the same cracking section (4), creating the reaction mixture (5) that, soon after, comes into contact with the main stream containing the traditional fossil load of a FCC (6) in a second cracking section (7).

Abstract: Additives for mixing into the base catalyst inventory of the fluid catalytic cracking (FCC) process units, so as to achieve a high selectivity of light olefins (ethylene and propylene), are described. Such additives comprise an FER zeolite and an MFI zeolite, the MFI zeolite preferably being zeolite ZSM-5. The mixture of the additive in a concentration greater than 2% w/w relative to the base catalyst of an FCC unit allows greater selectivity for light olefins, propylene and ethylene, while maintaining catalytic activity.

Abstract: The present invention relates to a process for obtaining fuel from biomass which comprises the introduction of the catalyst (3) in the base of an cracking section (4), wherein said catalyst (3) at high temperature comes in contact with a gas stream of light hydrocarbons rich in hydrogen (1), wherein the catalyst (3) and hydrocarbon (1) then come in contact with a lignocellulosic liquid stream (2) in the same cracking section (4), creating the reaction mixture (5) that, soon after, comes into contact with the main stream containing the traditional fossil load of a FCC (6) in a second cracking section (7).

Abstract: The present invention relates to a method for the production of ethene, CO, and hydrogen in a reactor with a circulating fluidized bed with two independent sections, from feedstocks that contain hydrocarbons with at least 11 carbon atoms or from feedstocks with a high oxygen content, using a catalyst in particulate form. The method teaches that in one of the sections of the reactor, in the absence of oxygen, a catalyst containing a dehydrogenation metal promotes the cracking of the said feedstocks, facilitating the subsequent endothermic reactions. In the other section, the coke is burned with air and the heating of the catalyst is controlled, for the adjustment of the appropriate amount of energy that the heated catalyst will convey to the section in which the endothermic reactions take place. The total ethene yield of the process according to the present invention is approximately 20% by weight in relation to the feedstock.

Abstract: Additives for mixing into the base catalyst inventory of the fluid catalytic cracking (FCC) process units, so as to achieve a high selectivity of light olefins (ethylene and propylene), are described. Such additives comprise an FER zeolite and an MFI zeolite, the MFI zeolite preferably being zeolite ZSM-5. The mixture of the additive in a concentration greater than 2% w/w relative to the base catalyst of an FCC unit allows greater selectivity for light olefins, propylene and ethylene, while maintaining catalytic activity.

Abstract: A process is described for maximization of light olefins, preferably ethylene, by the catalytic cracking of feeds of saturated hydrocarbons, with molecular size in the range from 4 to 6 carbon atoms. The process uses a catalyst based on a zeolite of type ZSM-5 with low sodium content and modified with nickel, with concentration by weight of nickel, expressed in the form of oxide, in the range from 0.1% to 20% relative to the weight of zeolite in the catalyst, and operating conditions that involve a temperature between 400° C. and 650° C. and feed partial pressure between 0.1 and 1.0 MPa, so that the product recovered is rich in light olefins, with ethylene/propylene ratio in the range from 0.25 to 2.00.

Abstract: The process combines hydroconversion and catalytic cracking starting from a feed containing triglycerides, at concentrations of fatty acids above 85%, which maximizes the yields of light olefins, chiefly ethylene and propylene, while reducing the yield of gasoline, with conversion greater than 80 wt. %.

Abstract: The present invention comprises a thermocatalytic cracking process for the production of diesel oil from a charge of vegetable origin made from seeds of oleaginous plants in refineries possessing at least two FCC reactors. At least one of such reactors processes heavy gas oil or residue under conventional conditions while at least one of such reactors processes the charge of vegetable origin made from seeds of oleaginous plants under conditions suitable, for production of diesel oil. Said process employs the same catalyst utilized in the fluid catalytic cracking process which, simultaneously, processes a conventional charge. The diesel, or biodiesel, oil produced by means of said process is of superior quality having a cetane number exceeding 40 given that the cracking reactions occur at low temperatures and the products obtained are less oxidized and consequently purer than products obtained by means of existing technology.

Abstract: A process is described for catalytic cracking of hydrocarbon feedstocks from petroleum refining which increases substantially the yields of light olefins. The process limits the extreme conditions to a first reaction section and introduces a stream of cooling fluid above the feedstock injection point so as to maintain a second reaction section under cracking conditions which produce light olefins propene and ethene, and inhibits reactions undesirable for the process.

Abstract: The present invention relates to a method of production of light olefins, with the objective of maximizing the production of propylene and in particular ethylene by the use of a special catalyst containing high-silica zeolite, whose composition also includes a dehydrogenating metal, so as to generate light olefins and appreciable deposition of coke on the catalyst. Gains in selectivity for light olefins are observed, and at the same time the energy deficiency of catalytic cracking in petrochemical operations with light hydrocarbons is minimized, avoiding problems due to the need to burn heating oil in the catalyst regenerating section to make up for the energy deficit of the converter.

Abstract: A process is described for maximization of light olefins, preferably ethylene, by the catalytic cracking of feeds of saturated hydrocarbons, with molecular size in the range from 4 to 6 carbon atoms. The process uses a catalyst based on a zeolite of type ZSM-5 with low sodium content and modified with nickel, with concentration by weight of nickel, expressed in the form of oxide, in the range from 0.1% to 20% relative to the weight of zeolite in the catalyst, and operating conditions that involve a temperature between 400° C. and 650° C. and feed partial pressure between 0.1 and 1.0 MPa, so that the product recovered is rich in light olefins, with ethylene/propylene ratio in the range from 0.25 to 2.00.

Abstract: The present invention relates to a system for the separation of suspensions of spent catalysts and hydrocarbons formed in an FCC unit with multiple ascending flow reaction tubes, comprising interconnections between each of the ascending flow reaction tubes and the separator vessel, each interconnection also comprises two sections. The outside sections of the separator vessel are inclined and are connected to a single vertical section, which penetrates into the interior of the separator vessel, and which has at its lower end an open device for draining the spent catalyst from the suspensions separated in this sector. In the same vertical section, at the end of its internal part at the separator vessel, a series of two sets of cyclones are installed, the first set containing cyclones without sealing legs, and the second set containing conventional cyclones of the first stage.

Abstract: A method is described for co-processing of ethanol and hydrocarbons from petroleum refining, which are introduced separately in two reaction zones of a reactor of a fluidized catalytic cracking unit. The process combines conversion of ethanol into ethene and conversion of hydrocarbons into other lighter hydrocarbon fractions, to produce ethene in quantities of 15 to 90 wt % in the fuel gas fraction obtained during the process.

Abstract: The present invention relates to a method for the production of ethene, CO, and hydrogen in a reactor with a circulating fluidized bed with two independent sections, from feedstocks that contain hydrocarbons with at least 11 carbon atoms or from feedstocks with a high oxygen content, using a catalyst in particulate form. The method teaches that in one of the sections of the reactor, in the absence of oxygen, a catalyst containing a dehydrogenation metal promotes the cracking of the said feedstocks, facilitating the subsequent endothermic reactions. In the other section, the coke is burned with air and the heating of the catalyst is controlled, for the adjustment of the appropriate amount of energy that the heated catalyst will convey to the section in which the endothermic reactions take place. The total ethene yield of the process according to the present invention is approximately 20% by weight in relation to the feedstock.