National Institute of Advanced Industrial Science and Technology

Agency of Industrial Science and Technology

Nissan Motor Company Limited

Nok Corporation

National Institute of Advanced Industrial Science

Makoto Toba

Fujio Mizukami

Shuichi Niwa

Yuji Yoshimura

Takehisa Mochizuki

Takashi Matsui

Kazuyuki Maeda

Shih-Yuan Chen

Nobuyuki Matsubayashi

Yuuji Yoshimura

Yohko Abe

Kazuhiko Haba

Tomonari Saito

Junichi Mine

Naotsugu Itoh

Kazuo Shimizu

Sumi Imai

Takemi Nanba

Hiroshi Shoji

Yoko Abe

Hirosi Shoji

The purpose of the present invention is to provide a method for producing a high quality biodiesel fuel having excellent oxidation stability and few low-temperature deposits. This purpose can be achieved by the following: hydrogenating a biodiesel fuel so as to selectively convert unsaturated fatty acid monoglycerides and then removing fatty acid monoglycerides through precipitation; or using an adsorbent to further remove fatty acid monoglycerides to a high degree from the biodiesel fuel produced using the method mentioned above.

Method for producing high quality biodiesel fuel

An object of the present invention is to provide a method for hydrogenating a biodiesel fuel for producing a biodiesel fuel having an excellent oxidation stability and cold flow property. The present invention serves to produce a biodiesel fuel excellent in oxidation stability, by hydrogenating a biodiesel fuel with oxygen present in the reaction system in the presence of a catalyst containing at least one type of noble metal selected from metals of Groups 8 to 10 in the periodic table.

Biodiesel fuel hydrogenation method

To provide a catalyst for production of a biodiesel fuel, which is capable of producing a biodiesel fuel with high selectivity, at a high yield, and at a low cost even in the presence of a water content and a free fatty acid, and a biodiesel fuel production method using the catalyst. Use of a titanium-containing mesoporous silica containing Ti and Si as skeleton constituent elements and having a pore diameter of 5 nm or greater as a transesterification catalyst enables a biodiesel fuel to be produced with high selectivity at a high yield through transesterification between an oil and an alcohol.

Transesterification catalyst and method for producing biodiesel fuel using transesterification catalyst

Provided is a method for producing biodiesel fuel having an excellent oxidative stability and fluidity at low temperature, wherein the method provides selective hydrogenation of a poly-unsaturated fatty acid alkyl ester to the mono-unsaturated fatty acid alkyl ester while inhibiting the formation of the trans-isomer, and a biodiesel fuel composition. In the method for producing biodiesel fuel, a fatty acid alkyl ester prepared from fat and/or waste edible oil by transesterification reaction, and/or (2) a fatty acid alkyl ester treated by esterification reaction of a fatty acid is hydrogenated in the presence of a hydrogenation catalyst containing at least one of noble metals selected from those of Groups 8-10 in the periodic table under low hydrogen pressure.

Method for producing biodiesel fuel and biodiesel fuel composition

A porous inorganic oxide support comprising an oxygen-containing carbonaceous material supported thereon, preferably a porous inorganic oxide support wherein the oxygen-containing carbonaceous material is a carbide of an oxygen-containing organic compound, wherein the ratio of the supported carbon amount with respect to the mass of the support for preparing the catalyst is from 0.05 to 0.2, the atomic ratio of the supported hydrogen amount with respect to the supported carbon amount is from 0.4 to 1.0, and the atomic ratio of the supported oxygen amount with respect to the supported carbon amount is from 0.1 to 0.6; and a hydrotreating catalyst of catalytic cracking gasoline which comprises the support and a catalyst containing a Group 8 metal of the periodic table, molybdenum (Mo), phosphorus and sulfur which is supported on the support are useful as a desulfurization catalyst of, for example, catalytic cracking gasoline at a hyperdesulfurized level, because of having functions of suppressing the hydrogenation activity of olefins and minimizing the decrease in the octane number even under reaction conditions with a high desulfurization ratio.

Porous inorganic oxide support and hydrotreating catalyst of catalytic cracking gasoline using the same

A hydrotreating catalyst comprising a Group 8 metal of the periodic table, molybdenum (Mo), phosphorus and sulfur, wherein the average coordination number [N(Mo)] of the molybdenum atoms around the molybdenum atom is from 1.5 to 2.5 and the average coordination number [N(S)] of the sulfur atoms around the molybdenum atom is from 3.5 to 5.0 when MoSstructure in the catalyst is measured in accordance with extended X-ray absorption fine structure (EXAFS) analysis.

Hydrotreating catalyst of catalytic cracking gasoline

A method for carrying out a reaction of one substance capable of being activated by a catalyst with another substance capable of reacting with said one substance activated, characterized in that the substance capable of being activated is activated by passing the substance through a diaphragm type catalyst and the reaction is thus performed in one reaction step; a method for producing an aromatic alcohol utilizing the above method; and a reaction apparatus suitable for these reactions. In the method, one substance is activated by passing through a diaphragm type catalyst and an objective reaction is carried out by using the activated substance, and the reaction can be performed in one reaction step and with safety. Moreover, the contact of the above activated substance with a compound to be reacted therewith can be freely controlled, and therefore, over-reaction can be prevented and an objective product can be produced in high yield. The method is thus markedly advantageous from an economical view point as a commercial process for producing oxygen-containing organic compounds such as an aromatic alcohol, a ketone, an aldehyde, a carboxylic acid and an epoxide.

Reaction method utilizing diaphram type catalyst and apparatus therefor

A process for preparing a cordierite, which includes dissolving a silicon compound, an aluminum compound and a magnesium compound in a molar ratio of 1:0.7 to 1:0.3 to 0.5 in a complexing agent represented by the formula R(OCH.sub.2 CH.sub.2).sub.n OH, wherein R is an alkyl group and n is an integer of 1 to 4; heating the resulting solution to bring about a ligand exchange reaction of the silicon compound, aluminum compound and magnesium compound with the complexing agent; conducting hydrolysis to form a gel; drying the gel and sintering the dried gel at 800.degree. to 1450.degree. C.

Process for preparing cordierite

A process of production of alumina includes method for controlling specific surface area of alumina. Control of specific surface area is performed by controlling porous structure of alumina. In the process, aluminum alkoxide is subject hydrolysis for forming alumina sol. During hydrolysis process, polyether is used as organic solvent in order to control the porous structure of produced alumina.

Method for controlling specific surface area of alumina

A mixture of a cyclodextrin and an alkoxy silane compound, e.g., tetraethoxy silane, is admixed with water and an acidic or alkaline catalyst, e.g., acetic acid, to effect ligand exchange and hydrolysis of the alkoxy silane followed by gelation into a gelled mass which is dried and, preferably, leached with water to remove excess of the cyclodextrin. The thus obtained gelled material is a composite having a structure in which the cyclodextrin molecules are incorporated into the matrix of amorphous silica presumably by forming Si-O-C linkages. The composite has characteristics as a combination of the properties of both of the component materials and can expand the applicability of the materials, for example, as a carrier of catalysts and immobilized enzymes, absorbent and adsorbent and so on.

Growing community of inventors

Ibaraki, Japan

Makoto Toba