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公开(公告)号:JP2003089662A
公开(公告)日:2003-03-28
申请号:JP2001285573
申请日:2001-09-19
Applicant: UBE INDUSTRIES
Inventor: NINOMIYA KOHEI , SUGIMOTO TSUNEMI , YAMANAKA MITSUO , KUGIMOTO JUNICHI , FUJITA TOSHIYUKI , FUNATSU JOJI
IPC: C07C7/04 , C07C7/148 , C07C7/20 , C07C13/277
Abstract: PROBLEM TO BE SOLVED: To provide a method for efficiently distilling crude cyclododecatriene with leaving little residue. SOLUTION: In the method for distilling crude cyclododecatriene by distillation, the distillation is carried out by controlling the content of peroxides included in the crude cyclododecatriene to
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公开(公告)号:JP2000210560A
公开(公告)日:2000-08-02
申请号:JP1513299
申请日:1999-01-25
Applicant: UBE INDUSTRIES
Inventor: SUGIMOTO TSUNEMI , YADA HIROHIDE , FUKUDA YASUNORI , MATSUZAKI TOKUO
Abstract: PROBLEM TO BE SOLVED: To enable a high decomposition performance to be maintained for a long time under practical reaction conditions by forming a catalyst for decomposing a gaseous compound containing fluorine from a perfluorocompound and/or a chlorofluorocarbon compound by adding a specific ratio of silicon dioxide to 100 γ-alumina. SOLUTION: The catalyst for decomposing a gaseous compound containing fluorine from a perfluorocompound and/or a chlorofluorocarbon compound is formed by adding 1-10 pts.wt. silicone dioxide to 100 pts.wt. γ-alumina. When this catalyst is used, the catalyst obtained by adding 1-10 pts.wt. silicon dioxide to 100 pts.wt. γ-alumina heated at 300-1,000 deg.C is brought into contact with a compound containing fluorine. Thus it is possible to maintain the high decomposition performance originally possessed by the γ-alumina to the compound containing fluorine for a long time by controlling the transition of the γ phase to the α phase which occurs in the alumina following a chemical reaction. Especially it is desirable to use the γ-alumina having 100 ppm or less Na content in terms of a metal.
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33.
公开(公告)号:JPH11179201A
公开(公告)日:1999-07-06
申请号:JP35071697
申请日:1997-12-19
Applicant: UBE INDUSTRIES
Inventor: ATOKUCHI TAKASHI , YADA HIROHIDE , SUGIMOTO TSUNEMI
Abstract: PROBLEM TO BE SOLVED: To continuously decomposite fluorine-contg. compds. including hardly decomposable perfluoro compds. under practical treatment conditions by prepar ing a catalyst showing high activity for continuous decomposition treatment of fluorine-contg. compds. from alumina having a specified Na amt. as a metal. SOLUTION: In the preparation of a catalyst having high activity for catalytic decomposition of fluorine-contg. compds. especially perfluoro compds. such as fluorocarbons, nitrogen fluoride and sulfur fluoride, an alumina having
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公开(公告)号:JPH09255628A
公开(公告)日:1997-09-30
申请号:JP7025496
申请日:1996-03-26
Applicant: UBE INDUSTRIES
Inventor: YAMAMOTO YOSHIFUMI , SUGIMOTO TSUNEMI , KURATO TOSHIO
Abstract: PROBLEM TO BE SOLVED: To readily produce a diaryl carbonate useful as a raw material for producing a polycarbonate at a sufficient rate of reaction by using a diaryl oxalate as a raw material with out using strongly toxic phosgene. SOLUTION: A diaryl oxalate is heated in the presence of an oxide of an alkaline earth metal in the vapor phase in a reactor to carry out the decarbonylating reaction. For example, diphenyl oxalate is cited as the diaryl oxalate and an oxide of magnesium, calcium, etc., is preferred as the oxide of the alkaline earth metal. The oxide may be supported on a catalyst carrier such as alumina, silica or active carbon for use. The decarbonylating reaction is preferably carried out under conditions of 200-600 deg.C, preferably about 300-500 deg.C and 10-10,000hr , preferably about 50-5,000hr space velocity by feeding a raw material gas containing an inert gas such as N2 gas to the reactor.
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公开(公告)号:JPH054897A
公开(公告)日:1993-01-14
申请号:JP15168991
申请日:1991-06-24
Applicant: KOKUSAI CHODENDO SANGYO GIJUTS , UBE INDUSTRIES , SHARP KK , FUJIKURA LTD
Inventor: SUGIMOTO TSUNEMI , SUGAWARA KAZUSHI , NAKAGAWA MIKIO , SHIOBARA TORU
IPC: C01G1/00 , C01G29/00 , C04B35/00 , C04B35/45 , C30B25/18 , C30B29/22 , H01B12/00 , H01B12/06 , H01B13/00 , H01L39/22 , H01L39/24
Abstract: PURPOSE:To provide the subject Bi-Sr-Ca-Cu-O-based superconductor film orientated in the direction of a or b axis to the base plate surface and suitable for production of a Josephson device, a three-terminal device, etc., and to provide a method for production thereof. CONSTITUTION:A Bi-Sr-Ca-Cu-O-based superconductor film formed on a base plate composed of an Mg0 (100) single crystal by chemical vapor phase growth method and preferentially growing in the direction of a or b axis to the base film surface. Film formation on the base plate composed of the MgO (100) single crystal is carried out by using chemical vapor phase growth method at =1.0nm/min film formation rate, thus providing the objective Bi-Sr-Ca-Cu-O-based superconductor film remarkably useful as a Josephson device, a three-terminal device, etc., by chemical vapor phase growth method.
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公开(公告)号:JPH04119923A
公开(公告)日:1992-04-21
申请号:JP23956890
申请日:1990-09-10
Applicant: KOKUSAI CHODENDO SANGYO GIJUTS , UBE INDUSTRIES , NEC CORP
Inventor: SUGIMOTO TSUNEMI , YOSHIDA MASAJI , SHIOBARA TORU , TANAKA SHOJI
Abstract: PURPOSE:To form a Bi-Sr-Ca-Cu-O supercomducting ultrathin film very useful for junction interface utilizing device by carrying out film formation by a chemical vapor deposition mothod at a specified rate of film formation in an atmosphere of an oxidizing gas. CONSTITUTION:Film formation is carried out by a chemical vapor deposition method at
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37.
公开(公告)号:JP2002080469A
公开(公告)日:2002-03-19
申请号:JP2001149699
申请日:2001-05-18
Applicant: UBE INDUSTRIES
Inventor: NINOMIYA KOHEI , SUGIMOTO TSUNEMI , KUGIMOTO JUNICHI , YAMANAKA MITSUO , KAIISO KOJI
IPC: C07B61/00 , C07D301/12 , C07D301/32 , C07D303/04
Abstract: PROBLEM TO BE SOLVED: To provide a process for purifying a reaction mixture from which 1,2-epoxy-5,9-cyclododecadiene can be separated by distillation, obtained from epoxidation of 1,5,9-cyclododecatriene with hydrogen peroxide in the presence of a catalyst comprising a tungsten compound, a quaternary onium salt and a mineral acid. SOLUTION: At least the oil layer in the epoxidation reaction mixture of 1,5,9-cyclododecatriene including the objective product, 1,2-epoxy-5,9- cyclododecadiene, the catalyst components, unreacting hydrogen peroxide and 1,5,9-cyclododecatriene is treated with an aqueous alkali. The oily layer may be separated before or after the alkali treatment.
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公开(公告)号:JPH11171830A
公开(公告)日:1999-06-29
申请号:JP33849497
申请日:1997-12-09
Applicant: UBE INDUSTRIES
Inventor: SUGIMOTO TSUNEMI , FUKUDA YASUNORI , MATSUZAKI TOKUO
IPC: B01J27/188 , C07B41/12 , C07B61/00 , C07C67/04 , C07C69/06
Abstract: PROBLEM TO BE SOLVED: To provide a method for easily separating a catalyst from a reaction mixture and enabling production of the objective compound in high yield in an industrially advantageous way, by adding a carboxylic acid to a cycloolefln in a two-liquid heterogeneous system consisting of a reaction mixture liquid phase and a heteropoly acid catalyst liquid phase. SOLUTION: This method comprises carrying out reaction in a two-liquid heterogeneous system consisting of a reaction mixture liquid phase and a heteropoly acid catalyst liquid phase, when a carboxylic acid is added to a cycloolefin. Preferably, this addition reaction is conducted at 60-150 deg.C and 1-20 kg/cm . To make the catalytic phase a liquid one, it is preferable that the heteropoly acid is previously treated under heating at 200-380 deg.C for 0.5-5 h in air or in, an inert gas atmosphere. The cycloolefin is preferably cyclooctene or cyclododecene. The carboxylic acid is, for example, acetic acid or propionic acid. It is preferable that the molar ratio of the carboxylic acid to cyclododecene is 5-20.
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39.
公开(公告)号:JPH11165071A
公开(公告)日:1999-06-22
申请号:JP33149297
申请日:1997-12-02
Applicant: UBE INDUSTRIES
Inventor: ATOKUCHI TAKASHI , YADA HIROHIDE , SUGIMOTO TSUNEMI
IPC: B01J21/02 , B01J27/053 , B01J27/16 , C07B35/06
Abstract: PROBLEM TO BE SOLVED: To continuously decompose a fluorine-containing compound containing also perfluoro-compound, which is difficult to decompose, by carrying a metal selected from group VIA, group VIII and group IIIB and an inorganic acid selected from sulfuric acid, phosphoric acid and boric acid on alumina. SOLUTION: The metal carried on the alumina is at least one or more kinds selected from group VIA, group VIII and group IIIB and Cr, Fe, Co, Ni, Pd and Pt, which are the transition metal elements, and B and Ga, which are the typical metal elements, among them produces good result. A preferable result is attained by controlling the quantity of the metal to be carried on the alumina carrier to 0.01-20 pts.wt. expressed in terms of metal per 100 pts.wt. carrier. The inorganic acid is limited to sulfuric acid, phosphoric acid and boric acid from the view point of the reaction condition and sulfuric acid having strong acidity and low splash property is most preferably used among them. The suitable result is attained by controlling the content of the inorganic acid in the catalyst to 0.1-20 pts.wt. per 100 pts.wt. alumina.
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公开(公告)号:JPH10286439A
公开(公告)日:1998-10-27
申请号:JP9715497
申请日:1997-04-15
Applicant: UBE INDUSTRIES
Inventor: ATOKUCHI TAKASHI , YADA HIROHIDE , SUGIMOTO TSUNEMI , MATSUZAKI TOKUO
IPC: A62D3/00 , B01D53/86 , B01J21/06 , B01J23/08 , B01J23/22 , B01J23/26 , B01J23/28 , B01J23/30 , B01J23/42 , B01J23/44 , B01J23/46 , B01J23/72 , B01J23/74
Abstract: PROBLEM TO BE SOLVED: To enable continuous decomposition of a perfluoro compd. by bringing a gaseous fluorine-contg. compd. into contact with molecular oxygen and water in the presence of catalyst prepared by depositing at least one kind of metal selected from among 4A, 5A, 6A, 7A, 8 and 1B groups and 3B groups on a carrier. SOLUTION: When a gaseous fluorine-contg. compd. (such as perfluoro compds. and fluorinated hydrocarbons) is decomposed, the fluorine-contg. compd. is brought into contact with molecular oxygen and water in the presence of a catalyst which is prepared by depositing at least one kind of metal selected from among 4A, 5A, 6A, 7A, 8, 1B and 3B groups on a carrier. As for the carrier, for example, alumina such as γ-alumina is preferably used. Its shape is not limited but properly selected according to the reactor and the reaction method. The amt. of the metal deposited is preferably 0.01 to 20 wt.% calculated as a metal to the carrier. As for the molecular oxygen, air is preferably used.
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