摘要:
A layered multimetallic oxide catalyst having the formula M1 M2 M3 Oδ wherein: M1 is selected from the group of Ag, Au, Zn, Sn, Rh, Pd, Pt, Cu, Ni, Fe, Co, an alkaline metal, an alkaline earth metal, a rare earth metal, and mixtures thereof; M2 is selected from the group of Ti, Hf, Zr, Sn, Bi, Sb, V, Nb, Ta and P, and mixtures thereof; M3 is selected from the group of Mo, W and Cr, and mixtures thereof; and where said multilayered metallic oxide exhibits a major X-ray diffraction peak between 5
摘要:
The present invention relates to a process for modifying the physical and chemical properties of Faujasite Y-type zeolites (FAU), mainly used as a base material of catalyst used in the Fluid Catalytic Cracking (FCC) process, for the interest of the oil refining industry, in which the conversion of oil heavy fractions into lighter fractions, with a higher commercial value, is carried out. The process produces a modified Faujasite Y-type zeolite, with lower sodium content, as low as 75%, than that of the starting Faujasite Y-type zeolite. A mesoporous material associated with the modified Faujasite Y-type zeolite has an average pore size ranging from 2 to 100 nm, having a bimodal or multimodal pore size distribution. The proportion of modified Faujasite Y-type zeolite with respect to the meso-porous material associated to the Faujasite Y type Zeolite can be regulated through the process operation conditions.
摘要:
The present invention relates to the preparation of Multimetallic Anionic Clays (MACs) through a simple method, which are then shaped by spray-drying into microspheres with adequate mechanical properties, suitable to be fluidized. The microspheres are appropriate for application as additives in the Fluid Catalytic Cracking (FCC) process, i.e. blended with the conventional catalyst, to in situ remove sulfur oxides (SOx) from the combustion gases produced in the regeneration stage of the FCC process, when cracking sulfur-containing hydrocarbon feeds. An oxidation promoter is added to the MACs in order to promote the oxidation of SO2 to SO3, a key step in SOx removal, providing more efficient and versatile materials, which are apt to be used in atmospheres with variable oxygen concentration.
摘要:
The present invention is related to a catalytic process, which includes catalytic compositions for depolymerisation and deoxygenation of lignin contained in the biomass for obtaining aromatic hydrocarbons. The catalytic composition consists of at least one non-noble element from group VIIIB of the periodic table supported on a mesoporous matrix composed of an inorganic oxide, which can be alumina surface-modified with a second inorganic oxide with the object of inhibiting the interaction between the active component and the support. The process of lignin depolymerisation consists of dissolving lignin in a mixture of protic liquids, reacting it I a reaction system by batch or in continuous flow at inert and/or reducing atmosphere, at a temperature of between 60 to 320° C. and a pressure of from 5 to 90 kg/cm2. When the reaction is developed into a batch system, oxygenated aromatic hydrocarbons are mainly produced, both by thermal as well as catalytic depolymerisation, whereas in a continuous flow reaction system, deoxygenated aromatic hydrocarbons are produced.
摘要:
The present invention is related to a catalytic process, which includes catalytic compositions for depolymerisation and deoxygenation of lignin contained in the biomass for obtaining aromatic hydrocarbons. The catalytic composition consists of at least one non-noble element from group VIIIB of the periodic table supported on a mesoporous matrix composed of an inorganic oxide, which can be alumina surface-modified with a second inorganic oxide with the object of inhibiting the interaction between the active component and the support. The process of lignin depolymerisation consists of dissolving lignin in a mixture of protic liquids, reacting it|a reaction system by batch or in continuous flow at inert and/or reducing atmosphere, at a temperature of between 60 to 320° C. and a pressure of from 5 to 90 kg/cm2. When the reaction is developed into a batch system, oxygenated aromatic hydrocarbons are mainly produced, both by thermal as well as catalytic depolymerisation, whereas in a continuous flow reaction system, deoxygenated aromatic hydrocarbons are produced.