序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
181 Conversion of chlorinated alkene into less chlorinated useful substance JP19407794 1994-08-18 JPH07149680A 1995-06-13 RARII ENU ITOO; EE DEIRU HAAREE; MAIKERU TEII HORUBURUTSUKU; DEBITSUDO DEII SUMISU; KUREIGU BII MAACHISON
PURPOSE: To convert a chlorinated hydrocarbon into a less chlorinated product, and to obtain a catalyst used therein. CONSTITUTION: A chlorinated alkene feedstock containing two or more chlorine atoms is converted into a reaction product containing a less chlorinated alkene at a commercially substantial proportion. The chlorinated alkene feedstock is allowed to react with hydrogen in the presence of a catalyst substantially comprising a group VIII metal or a group IB metal other than rhodium, palladium or ruthenium on a support. COPYRIGHT: (C)1995,JPO
182 Catalytic transfer hydrogenation by aromatic nitro compound as hydrogen receptor JP12603288 1988-05-25 JPS63316741A 1988-12-26 TOONI DOTSUKUNAA; HERUBERUTO KURUUBU; MANFUREETO ZAUERUWARUTO
183 Selective production of perhydroacenaphthene cis form JP10796986 1986-05-12 JPS62265238A 1987-11-18 NARUSE YOSHIHIRO; SUZUKI TOSHIHIDE
PURPOSE: To obtain the titled substance useful as a high-boiling oil or an intermediate for synthesizing adamantanes in high yield and selectively, by hydrogenating acenaphthene in the presence of a ruthenium type and/or rhodium type catalyst at a specific temperature. CONSTITUTION: In obtaining the titled substance by hydrogenating acenaphthene, the reaction is carried out in the presence of a ruthenium type and/or a rhodium type catalyst at 80W200°C for 20minW4hr. A catalyst having carbon as a carrier is preferable and the amount of the catalyst used is preferably 0.5W2wt% based on acenaphthene. EFFECT: By using the above-mentioned method, perhydroacenaphthene is obtained in high yield and cis-form having the maximum boiling point can be selectively obtained. COPYRIGHT: (C)1987,JPO&Japio
184 JPS62502402A - JP50196086 1986-03-27 JPS62502402A 1987-09-17
185 Production of catalyst carrier JP14465986 1986-06-20 JPS6238240A 1987-02-19 CHIYAARUZU ARUFURETSUDO DOREIK
186 JPS5926333B2 - JP10646475 1975-09-01 JPS5926333B2 1984-06-26 JON JEEMUZU MATSUKAAROORU; JON TOREBAA KENTO KURAAKU; SUCHIIFUAN ROBAATO TENISON
187 Condensation of natural gas or methane to gasoline zone hydrocarbons JP15248182 1982-09-01 JPS5874783A 1983-05-06 JIYOOJI ANDORIYUU UURAA
188 JPS5822129B2 - JP2262481 1981-02-17 JPS5822129B2 1983-05-06 SHIMIZU KAZUO
189 Cyclohexylphenyl derivatives, dielectric body and electronically optical display element JP17152281 1981-10-28 JPS5799537A 1982-06-21 MIHAERU REMERU; YOAHIMU KURAUSU; RUUTOBUITSUHI POORU
190 Manufacture of 1*77octadiene JP3516079 1979-03-27 JPS54132507A 1979-10-15 KENJI NOZAKI
191 Synthesis of hydrocarbons from co and h2 by using ruthenium supported by vb group metal oxide JP12901378 1978-10-19 JPS5470205A 1979-06-05 EMU ARUBAATO BUANNAISU; SAMIERU JIEI TOOSUTAA
192 Novel carbonaceous matter and method of producing high calorific gas from said matter JP8891178 1978-07-20 JPS5448806A 1979-04-17 MAKUSHIMIRIAN BAAKU; JIYATSUKU RUISU BURUMENTARU
193 Process for preparing ethene JP9656178 1978-08-08 JPS5436203A 1979-03-16 HERUSHIO BARURADARESU BARUROKA; YOAO BAPUTEISUTA DE KASUTORO E; RUI KOUTEINHO DE ASUSHISU
194 Hexahydroterphenyl derivative JP324978 1978-01-13 JPS5390251A 1978-08-08 RUDORUFU AIDENSHINKU; YOAHIMU KURAUZE; RUUDEITSUHI POORU
195 Preparation of styrene JP5300377 1977-05-09 JPS52136133A 1977-11-14 AIIDERU HOWAAN
196 JPS5221479B2 - JP7942571 1971-10-11 JPS5221479B2 1977-06-10
197 Catalysts and method for reducing carbon monoxide JP12478376 1976-10-18 JPS5250988A 1977-04-23 BIRUHERUMU FUOOKUTO; HERUMAN KURAAZERU; YURUGEN KOTSUHO
198 Platinum group metal catalysts JP10646475 1975-09-01 JPS51125693A 1976-11-02 JIYON JIEEMUZU MATSUKAAROORU; JIYON TOREBAA KENTO KURAAKU; SUCHIIFUAN ROBAATO TENISON
199 JPS5120195B1 - JP9485671 1971-11-25 JPS5120195B1 1976-06-23
200 JPS511233B1 - JP9457771 1971-11-26 JPS511233B1 1976-01-14
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