Chiyoda Corporation

Nkk Corporation

Chiyoda Chemical Engineering Construction Co., Ltd.

Kenji Shimokawa

Yoshimi Shiroto

Takeshi Minami

Mitsunori Shimura

Hiroaki Taniguchi

Yakudo Tachibana

Yoshio Fukui

Kazuhiko Tate

Kazuhiko Hamato

Sachio Asaoka

Noriyuki Yoneda

Toshiji Makabe

Osamu Togari

Masatoshi Matsuda

Hiroto Tajima

Kazuaki Ueda

In the production step, alcohol is reacted with carbon monoxide in a reaction solvent in the presence of a rhodium-containing solid catalyst obtained by immobilizing rhodium in an insoluble carrier (I) containing a pyridine ring in its resin structure and an alkyl iodide containing an alkyl group of 1 to 5 carbon atoms, to produce a reaction product having a water content of 0.5 to 10% by weight; and in the subsequent removing step, an organic carboxylic acid is separated and recovered from the reaction product, and the recovered organic carboxylic acid is contacted with an insoluble carrier (II) containing a pyridine ring in its resin structure, to remove an iodide contained in the organic carboxylic acid.

Process for preparing organic carboxylic acid

A methanol carbonylation catalyst includes a rhodium complex supported on a porous, cross-linked vinylpyridine resin, wherein the vinylpyridine resin has a cross-linking degree of 30-60%, a pore volume of 0.1-0.4 ml/g and an average pore diameter of 20-100 nm. The catalyst may be prepared by contacting the pyridine ring-containing resin with an aqueous solution containing rhodium ion and then contacting the resulting rhodium ion-carrying resin with carbon monoxide and an alkyl iodide in an organic solvent to convert the rhodium ion to a rhodium complex bound to the resin. Acetic acid is produced by reacting carbon monoxide with methanol at a temperature of 140.degree.-250.degree. C. and a partial pressure of carbon monoxide of 7-30 kg/cm.sup.2 in the presence of an alkyl iodide and the above catalyst.

Supported rhodium catalyst, method of preparing same and process of

A method of separating 2,6-diisopropylnaphthalene from a mixture containing 2,6-diisopropylnaphthalene and structural isomers thereof including the 2,7-isomer is disclosed, wherein the mixture is first subjected to a selective adsorption and desorption treatment using a zeolite absorbent capable of adsorbing the 2,7-isomer to obtain a first extract containing the sorbed 2,7-isomer and a first raffinate containing non-sorbed isomers including the 2,6-isomer, the 2,6-isomer being thereafter separated from the first raffinate.

Method of separating 2,6-diisopropylnaphthalene from a mixture

A process for the production of 2,6-diisopropylnaphthalene is disclosed wherein an isopropylation reaction mixture containing isopropylated naphthalenes is subjected to transalkylation with a triisopropylnaphthalene-containing mixture to obtain a mixture containing mono-, di- and tri-isopropylnaphthalenes which is then separated into a first fraction containing monisopropylnaphthalenes, a second fraction containing diisopropylnaphthalenes and a third fraction containing triisopropylnaphthalenes. The first and third fractions are recycled to the above system, while the second fraction is subjected to separation treatments for the recovery of 2,6-diisopropylnaphthalene. The second fraction from which 2,6-diisopropylnaphthalene has been removed is subjected to transalkylation with naphthalene to obtain a monoisopropylnaphthalene-rich mixture which is to be fed to the isopropylation step.

Process for the production of 2,6-diisopropylnaphthalene

A catalyst for hydrocracking heavy hydrocarbon oils includes a porous inorganic carrier composed mainly of alumina or titania, and two or more catalytic metal components composited with the carrier. The metals of the catalytic metal components are either (a) V and at least one element selected from Zn, Fe, Co, Ni, Cu, Ag, Sn and Pb or (b) Mo and at least one element selected from Zn, Cu, Ag, Sn, Pb and the lanthanum-series elements. The catalyst has at least 60% of its total pore volume in pores with a diameter of 200 .ANG. or more, at least 40% of its totalpore volume in pores with a diameter of 300 .ANG. or more and not more than 20% of its total pore volume in pores with a diameter of at least 1000 .ANG.. Disclosed also is a process for hydrocracking a heavy hydrocarbon oil in the presence of the above catalyst.

Process for hydrocracking heavy hydrocarbon oils and catalyst therefor

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Yokohama, Japan

Kenji Shimokawa