Abstract: The present invention relates to a process for preparing a bio-diesel, comprising the steps of, in the presence of an additional free fatty acid source, reacting a raw oil-fat with C1-C6 monohydric alcohol in a reactor, and separating fatty acid esters from the reacted materials, so as to produce the bio-diesel, wherein the amount of the free fatty acid in the free fatty acid source ranges from 2-100 wt % and is higher than the amount of the free fatty acid in the raw fat-oil. The present process can increase the fatty acid ester yield and purity of raw oil-fats having a low reaction activity, and has a high adaptability to raw materials.

Abstract: The present invention provides a process for preparing a bio-diesel, comprising, in the presence of an alkaline metal compound, reacting an oil-fat with C1-C6 monohydric alcohol in a reactor at a reaction temperature of from 130 to 280° C. and a reaction pressure of from 1 to 12 MPa, separating fatty acid esters from the reacted materials, so as to produce the bio-diesel, wherein said alkaline metal compound is present in an amount of 0.001-0.07 wt %, in terms of the metal thereof, relative to the weight of the oil-fat. The process provided in the present invention has the advantages of great throughput and high yield of the bio-diesel.

Abstract: The present invention provides a process for preparing a bio-diesel, comprising, in the presence of an alkaline metal compound, reacting an oil-fat with C1-C6 monohydric alcohol in a reactor at a reaction temperature of from 130 to 280° C. and a reaction pressure of from 1 to 12 MPa, separating fatty acid esters from the reacted materials, so as to produce the bio-diesel, wherein said alkaline metal compound is present in an amount of 0.001-0.07 wt %, in terms of the metal thereof, relative to the weight of the oil-fat. The process provided in the present invention has the advantages of great throughput and high yield of the bio-diesel.

Abstract: The present invention relates to a process for preparing a bio-diesel, comprising the steps of, in the presence of an additional free fatty acid source, reacting a raw oil-fat with C1-C6 monohydric alcohol in a reactor, and separating fatty acid esters from the reacted materials, so as to produce the bio-diesel, wherein the amount of the free fatty acid in the free fatty acid source ranges from 2-100 wt % and is higher than the amount of the free fatty acid in the raw fat-oil. The present process can increase the fatty acid ester yield and purity of raw oil-fats having a low reaction activity, and has a high adaptability to raw materials.

Abstract: A Y-zeolite-containing composite material made from materials comprising kaolin by in-situ crystallization, said composite material comprises nest-like structure. Content of Y-zeolite is in the range of 30–85% by weight of said composite material. The nest-like structure is essentially comprised of rodlike crystal, further comprises flaky crystal or blocky crystal. Y-zeolite in the composite material may be HY, REY, or REHY. Said composite material is suitable to be used as catalysts for catalytic cracking of heavy oil or resid. The invention further relates to a process for preparing the composite material.

Abstract: The present invention relates to a cracking catalyst comprising layered clays and a process for cracking hydrocarbon oils using said catalyst. Said catalyst is prepared by the process comprising the following steps: mixing and slurrying an expandable clay, a modifier component, pseudo-boehmite and water for 0.1-10 h to obtain a slurry, aging the slurry at 50-85° C. for 0.1-10 h, then drying and forming the slurry to obtain a formed material, water washing and aging the solid, and finally drying and calcining the solid, and said modifier being one or more selected from the group consisting of hydroxyl polymers of silicon, aluminum, zirconium or titanium, and substances comprising one or more of said hydroxyl polymers.

Abstract: A process for adsorptive desulfurization of gasoline or diesel oil or aromatics lower than C12 containing organic sulfide impurities, wherein these feedstocks contact an amorphous alloy adsorbent comprising nickel as a major active component in a fluidized bed reactor or a magnetic-stabilized fluidized bed reactor or a slurry bed reactor. There is only a single diffuse peak at 2?=45° in the 2? range from 20° to 80° in the X-ray diffraction (XRD) pattern of the adsorbent. The adsorbent consists of 50-95 wt % of nickel, 1-30 wt % of aluminum, 0-35 wt % of iron, and 0-10 wt % of one or more metals selected from copper, zinc, molybdenum, chromium, and cobalt.

Abstract: A Y-zeolite-containing composite material made from materials comprising kaolin by in-situ crystallization, said composite material comprises nest-like structure. Content of Y-zeolite is in the range of 30-85% by weight of said composite material. The nest-like structure is essentially comprised of rodlike crystal, further comprises flaky crystal or blocky crystal. Y-zeolite in the composite material may be HY, REY, or REHY. Said composite material is suitable to be used as catalysts for catalytic cracking of heavy oil or resid. The invention further relates to a process for preparing the composite material.

Abstract: The present invention relates to a cracking catalyst comprising layered clays and a process for cracking hydrocarbon oils using said catalyst. Said catalyst is prepared by the process comprising the following steps: mixing and slurrying an expandable clay, a modifier component, pseudo-boehmite and water for 0.1-10 h to obtain a slurry, aging the slurry at 50-85° C. for 0.1-10 h, then drying and forming the slurry to obtain a formed material, water washing and aging the solid, and finally drying and calcining the solid, and said modifier being one or more selected from the group consisting of hydroxyl polymers of silicon, aluminum, zirconium or titanium, and substances comprising one or more of said hydroxyl polymers.

Abstract: A process for adsorptive desulfurization of gasoline or diesel oil or aromatics lower than C12 containing organic sulfide impurities, wherein these feedstocks contact with a amorphous alloy adsorbent comprising nickel as a major active component in a fluidized bed reactor or a magnetic-stabilized fluidized bed reactor or a slurry bed reactor. There is only a single diffuse peak at 2&thgr;=45° in the 2&thgr; range from 20° to 80° in the X-ray diffraction (XRD) pattern of the adsorbent. The adsorbent consists of 50-95 wt % of nickel, 1-30 wt % of aluminum, 0-35 wt % of iron, and 0-10 wt % of one or more metals selected from the group consisting of copper, zinc, molybdenum, chromium, and cobalt.

Abstract: An amorphous alloy catalyst for hydrogenation and its preparation method are disclosed herein. The catalyst essentially consists of nickel ranging between 60 and 98 wt %, iron ranging between 0 and 20 wt %, one doping metal element selected from the group consisting of chromium, cobalt, molybdenum, manganese and tungsten ranging between 0 and 20 wt %, and aluminum ranging between 0.5 and 30 wt % based on the weight of said catalyst, wherein the weight percentages of iron and the doping metal element component may not be zero at the same time; and just one broad diffusion peak appears at about 2 &thgr;=45±1° on the XRD patterns of the catalyst within 2 &thgr; range from 20 to 80°. The catalyst herein can be used in processes for hydrogenation of unsaturated compounds such as olefin, alkyne, aromatics, nitro, carbonyl groups, nitrile and soon, and for hydrorefining of caprolactam in particular.

Abstract: A process for alkylation of an isoparaffin with an olefin comprising contacting an isoparaffin containing feed with an olefin-containing feed in the presence of a catalyst, said catalyst is a supported heteropoly acid catalyst, which is represented by the following chemical formula: HkYWmMo12-nO40·nH2O, wherein k is 3 or 4, Y is an atom of P, Si, Ge or As, m is a positive integer between 0-12, n is any number in the range of >0-10; the reaction temperature is at least equal to the critical temperature of isoparaffin and up to 300° C.; the reaction pressure is at least equal to the critical pressure of isoparaffin. The advantages of this process are embodied in high olefin conversion, high alkylate yield, and good retention of catalyst stability at the same time.

Abstract: A conversion process of hydrocarbon oils comprises at least a hydrodemercaptanization process, wherein said hydrodemercaptanization process comprises contacting a feedstock with a hydrofining catalyst containing a tungsten oxide and/or a molybdenum oxide, a nickel oxide and a cobalt oxide supported on an alumina under the conditions of hydrodemercaptanization, in which the content of said tungsten oxide and/or molybdenum oxide is from 4 wt % to less than 10 wt %, the nickel oxide content is 1-5 wt %, the cobalt oxide content is 0.01-1 wt % based on the catalyst, and the ratio of total atom number of nickel and cobalt to total atom number of nickel, cobalt, tungsten and/or molybdenum is 0.3-0.9. Said process can be carried out at a lower temperature and a lower H/oil volume ratio.

Abstract: An amorphous alloy catalyst containing nickel and phosphorus comprising a porous carrier, a Ni--P amorphous alloy supported on the carrier, and a pre-supported catalytic component for inducing and catalyzing the formation of the Ni--P amorphous alloy onto the carrier. In a preferred embodiment, the catalyst contains 0.15-30 wt % of Ni, based on the total weight of the catalyst, 0.03-10 wt % of P, based on the total weight of the catalyst, 0.01-3.5 wt % of B, based on the total weight of the catalyst. The nickel exists in the form of Ni--P or Ni--B amorphous alloy, the atomic ration Ni/P in the Ni--P amorphous alloy is in range of 0.5-10, the atomic ratio Ni/B in the Ni--B amorphous alloy is in range of 0.5-10. The catalyst may further comprise from 0.01 to 20 wt % of a metal additive (M), based on the total weight of the catalyst. The metal additive (M) refers to one or more metal elements, except Ni, which can be reduced from the corresponding salt into its elemental form.

Abstract: A hydrotreating catalyst containing molybdenum and/or tungsten for light oil distillates, said catalyst contains tungsten oxide and/or moybdenum oxide, nickel oxide and cobalt oxide supported on an alumina carrier, the content of said tungsten oxide and/or molybdenum oxide is from 4 wt % to less than 10 wt %, the content of nickel oxide 1.about.5 wt %, the content of cobalt oxide 0.01.about.1 wt %, the atom ratio of nickel-cobalt to nickel, cobalt-tungsten and/or molybdenum is 0.3.about.0.9. Compared with the prior art, the catalyst has lower metal content, but higher activity at low-temperature. The catalyst is especially suitable for use in the hydrodemercaptanization process of light oil distillates.

Abstract: The present invention discloses an amorphous alloy catalyst containing boron, which is composed of a porous carrier, a Q-B amorphous alloy, and a metal additive (M), the content of Q-B amorphous alloy together with metal additive is from 0.1 to 60 wt %, based on the total weight of the catalyst, in which the atomic ratio (Q+M)/B is 0.5-10, and the Q/M atomic ratio is 0.1-1000; wherein Q represents an metal selected from group VIII and B represents boron; and said metal additive (M) refers to those one or more metal elements which can be reduced to its/their elemental states from the corresponding salts by a solution containing BH.sub.4.sup.- with the exception that M is not the one which is used as Q. Said catalyst exhibits high catalytic hydrogenation activity.

Abstract: Disclosed is a process for continuous alkylation of aromatics or their derivatives in the presence of a solid acid catalyst in a liquid-solid circulating fluidized bed system, said system comprising a liquid-solid cocurrent upflow reactor, a sedimentation washing tower for the used catalyst, a liquid-solid cocurrent upflow regenerator, a sedimentation washing tower for the regenerated catalyst, and two vortical liquid-solid separators. By regeneration of the used catalyst, continuous alkylation process is achieved in this system.

Abstract: A class of pillared interlayered clay molecular sieves with large pore size were prepared by cross-linking the regularly interstratified mineral clay. Wherein the cross-linked rectorites possess an extraordinary thermal and hydrothermal stabilities. Said class of pillared interlayered clay molecular sieves are potential commercial catalysts for carbonium-ion type reactions, adsorbents and catalyst carriers.