Mitsui Toatsu Chemicals, Incorporated

Mitsui Chemicals, Inc.

Petroleum Energy Center

Masamitsu Inomata

Minato Karasawa

Hiroshi Ozawa

Tetsuya Oishi

Kanemitsu Miyama

Atsuyoshi Yamauchi

Hiroharu Kageyama

Izumi Mega

Hiroshi Ono

Sinji Tokunoh

Kazuo Sugazaki

Jin Suzuki

Kouhei Ohkawa

Satoshi Furusawa

Kazunori Kamada

Akito Watanabe

Tatsunobu Nakashima

Katsumi Sakamoto

Shigeru Nakahata

Takeshi Hiraiwa

Kenichi Yamamoto

Kenji Fujiwara

Isao Fukada

Hiroki Mizutani

Yoshimitsu Kokubu

Harushige Sugawara

Takeshi Oomatsuzawa

Akio Numa

Masahiro Tokumitsu

Masahiro Takeno

Masanobu Ebina

Methanol is produced by reacting carbon monoxide and hydrogen in the presence of a Raney copper catalyst containing 80 to 99.9 wt. % of copper in a solvent. The catalysts employed in the present invention showed a much higher activity even under the conditions of a low temperature in methanol production, than any of the known catalysts. The process of the methanol production may eliminate necessity for recycling an unreacted synthesis gas into the reaction system, and makes it feasible to conduct methanol synthesis at a lower pressure than conventional processes.

Process for methanol production

In a process for preparing a Diels-Alder addition product of a conjugated diolefin and acrylonitrile by reacting the conjugated diolefin with acrylonitrile, a vessel type reactor is used. The pressure of the gaseous phase in the reactor is increased by using an inert gas in the reaction. A premixed solution of the conjugated diolefin or a compound which produces the conjugated diolefin in the reactor and acrylonitrile is released through an upper portion of the reactor into the gaseous phase and then dropped into a liquid phase to react. A reaction product is taken out through a lower portion of the reactor. The process can be carried out continuously in a safe manner over an extended period of time without any adhesion of an insoluble polymer to the reactor or to the inlet or outlet pipes, and without sudden pressure fluctuations.

Process for preparing diels-alder addition product from conjugated

Provided by the present invention are novel diguanamine derivatives, led by 2,5/2,6-bis(4,6-diamino-1,3,5-triazin-2-yl)-bicyclo[2.2.1]heptanes and 1,3/1,4-bis(4,6-diamino-1,3,5-triazin-2-yl)-cyclohexanes, and derivatives thereof, applications of these compounds in fields such as adhesives and paints, utilization of these compounds in flame-retarding, thermal stabilization and compatibilization methods of resins, thermosetting molding compositions and thermosetting expansion-molding compositions making use of these compounds, as well as polymeric microspheres also using these compounds. These compounds are expected to find wide spread industrial utility as various excellent properties can be obtained by using them.

Diguanamines and preparation process, derivatives and use thereof

Alpha-hydroxy-isobutyramide is produced by continuously hydrating acetone cyanohydrin in a liquid phase in the presence of a manganese dioxide catalyst and in the presence of a particular oxide dissolved in water, oxoacid, heteropolyacid or a salt of the acids.

Process for producing .alpha.-hydroxy-isobutyramide

Amides are produced by reacting nitriles with water in a liquid phase in the presence of a manganese oxide containing an element selected from Groups IIIA, IVA, VA, IIIB, IVB, VB , VIB and VIII of the Periodic Table.

Process for producing amide compounds

An .alpha., .beta.-unsaturated carboxylic acid is produced by catalytically reacting an .alpha.-hydroxycarboxylic acid amide of the formula (1), ##STR1## where R.sub.1 and R.sub.2 are independently selected from the group consisting of hydrogen and C.sub.1 -C.sub.4 alkyl groups, provided that at least one of R.sub.1 and R.sub.2 is the alkyl group, with water in the presence of a solid acid catalyst containing a high surface area rare earth phosphate anhydride having the monoclinic system structure producible by heating a rare earth phosphate of the hexagonal system structure at 60.degree.-200.degree. C. in a solution of an inorganic acid, an inorganic acid salt and/or an inorganic acid ester where the molar ratio of the inorganic acid component to the rare earth phosphate of the hexagonal system structure is 0.5-400.

Process for producing .alpha., .beta.-unsaturated carboxylic acid

.alpha.,.beta.-Unsaturated carboxylic acid esters are produced by a catalytic reaction of .alpha.,.beta.-unsaturated carboxylic acids and/or .alpha.,.beta.-unsaturated carboxylic acid amides with aliphatic alcohols in the presence of a solid acid catalyst comprising zirconium oxide, titanium oxide or a composite oxide thereof containing phosphorus.

Process for producing .alpha.,.beta.-unsaturated carboxylic acid esters

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Chiba, Japan

Masamitsu Inomata