首页 / 专利分类库 / 有机化学 / 无环或碳环化合物 / 含有卤原子的无环饱和化合物
序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
81 Combined apparatus of filter*package and method of recovering melt hexachlorobenzene byproduct by using said apparatus JP176079 1979-01-10 JPS54100327A 1979-08-08 JIYON ROSU BURANKU; GUREN FURANKU ROZUMASU
82 Preparation of 1,1-dilalogenated aliphatic compounds JP1869077 1977-02-24 JPS53105403A 1978-09-13 KOUNO HIROMICHI; NAGAI YOUICHIROU; MATSUMOTO HIDEYUKI
PURPOSE: To prepare 1,1-dihalogenated aliphatic compounds easily in high yield, by the reduction of 1,1,1-trihalogenated aliphatic compounds with silane in the presence of a phosphine-group VIII transition metal complex catalyst. COPYRIGHT: (C)1978,JPO&Japio
83 Oxychlorination of hydrocarbons or partially chlorinated hydrocarbons JP13014476 1976-10-29 JPS5356601A 1978-05-23 KOBAYASHI YASUSHI; ARITAKI MASATO; SHIMIZU TAKAAKI
PURPOSE: To carry out oxychlorination reaction of hydrocarbons or partially chlorinated hydrocarbons, with suppressing direct oxidation of raw materials and without lowering the conversion of hydrochloric acid, by use of a mixed molten salt, which comprises copper chloride, and lead chloride, etc. as a catalyst. COPYRIGHT: (C)1978,JPO&Japio
84 Separation by distillation of chlorinated hydrocarbons having two or more carbon atoms. JP9527976 1976-08-09 JPS5321104A 1978-02-27 KATAOKA ARINOBU; TAKAHASHI TAKEO; AGEO KEIZOU; KISHIDA HIROSHI
PURPOSE: When chlorinated hydrocarbons of 2 or more carbon atoms are separated by distillation, water, alcohols, phenols or amines are added before or at the time of distillation, to obtain highly pure chlorinated hydrocarbons free from CCl 4. COPYRIGHT: (C)1978,JPO&Japio
85 JPS5129122B2 - JP7364671 1971-09-20 JPS5129122B2 1976-08-24
86 Ensokatankasuisono seizohoho JP399675 1974-12-28 JPS5180802A 1976-07-15 KOYANAGI SHUNICHI; KOBAYASHI YASUSHI; ARITAKI MASATO
87 JPS5037642B1 - JP5986170 1970-07-10 JPS5037642B1 1975-12-04
88 JPS50112305A - JP2268674 1974-02-26 JPS50112305A 1975-09-03
89 JPS5069039A - JP11854273 1973-10-23 JPS5069039A 1975-06-09
90 JPS5047983A - JP8471974 1974-07-25 JPS5047983A 1975-04-28
91 JPS4988877A - JP14252773 1973-12-21 JPS4988877A 1974-08-24
92 方法 JP2017539498 2015-10-15 JP2017532380A 2017-11-02 オンドルス ズデニェク; クビツェク パベル; フィラス カレル; スラデク ペトル
高純度1,1,1,2,3−ペンタクロロプロパン生成物を調製する方法であって:1−a)エチレン、四塩化炭素、及び触媒を含む反応混合物を主要アルキル化領域に提供して、前記反応混合物中に1,1,1,3−テトラクロロプロパンを生じることと、1−b)工程1−a)で得た反応混合物を処理して、1,1,1,3−テトラクロロプロパン原料を得ることと;2−a)1,1,1,3−テトラクロロプロパン原料を脱塩化素反応領域で触媒と接触させて、1,1,1,3−テトラクロロプロパン及び1,1,3−トリクロロプロペンを含む反応混合物を生じることと、2−b)工程2−a)で得た前記反応混合物を処理して、1,1,3−トリクロロプロペン原料を得ることと;3−a)前記1,1,3−トリクロロプロペン原料を反応領域で塩素と接触させて、1,1,1,2,3−ペンタクロロプロパン及び1,1,3−トリクロロプロペンを含む反応混合物を生じることであって、前記反応領域は前記脱塩化水素反応領域とは異なる、ことと、3−b)工程3−a)で得た反応混合物を処理して、高純度1,1,1,2,3−ペンタクロロプロパン生成物を得ることとを含む、方法を開示する。【選択図】図1
93 Composition for alkylation and method for detoxication of harmful compound using the same composition JP2006118388 2006-04-21 JP2008050265A 2008-03-06 NAKAMURA KOICHIRO; HISHINUMA AKIMITSU; KAMIYA SHINJI; DOKEN SHINJIRO
PROBLEM TO BE SOLVED: To obtain a composition for alkylation, useful for detoxication of inorganic arsenic, etc., and to provide a safe and high-efficiency method for detoxication using the composition. SOLUTION: The composition for alkylation contains an organometallic complex having a cobalt-carbon bond. The detoxication method comprises alkylating a harmful compound containing at least one kind of an element selected from the group consisting of arsenic, antimony and selenium in the presence of the composition so as to detoxicate the harmful compound. COPYRIGHT: (C)2008,JPO&INPIT
94 Production method of zinc chloride carrier JP2002336122 2002-11-20 JP4056366B2 2008-03-05 光男 成田; 和久 早川; 正樹 田畑
95 Discharge decomposing device for organohalogen compound and method of the same JP2004055537 2004-02-27 JP2005238206A 2005-09-08 AOI TATSUFUMI; YAMASHITA ICHIRO; IKEDA TETSUYA; TONAKA HIDEKI; NAKATANI IKUO; HORI KEIICHI
<P>PROBLEM TO BE SOLVED: To provide a discharge decomposing device for an organohalogen compound capable of a stable continuous operation without causing damages on a discharge tube or other components due to the occurrence of an abnormal discharge, and a method of the same. <P>SOLUTION: This organohalogen compound discharge decomposing device, in which a thermal plasma is generated by throwing energy using microwaves into a gas containing the organohalogen compound and the organohalogen compound is decomposed in the thermal plasma, is provided with a controller 19 which serves to make the ignition energy thrown when igniting the thermal plasma smaller than the maintenance energy for maintaining the ignited thermal plasma as a thermal plasma exerting decomposability. <P>COPYRIGHT: (C)2005,JPO&NCIPI
96 Reaction tube for organic halogen compound cracking apparatus JP2000318444 2000-10-18 JP2002126500A 2002-05-08 SUZUKI KAZUHIRO; MATSUMOTO SOICHIRO; OKADA YUJI
PROBLEM TO BE SOLVED: To provide a reaction tube for an organic halogen compound cracking apparatus which is capable of assuring both of desired heat resistance and corrosion resistance. SOLUTION: The reaction tube has a cylindrical shape in cross section and has a reaction tube upper part connected to the terminal of a plasma discharge tube and a reaction tube lower part connected across a gasket 51 to the reaction tube upper part. The approximately annular planar gasket 51 has a core material 52 which consists of an approximately annular planar asbestos-base gasket, covering parts 53 which consists of, for example, carbon-base gasket disposed to cover the outside surface, i.e., front surface 52A and rear surface 52B as well as inner peripheral surface 52C and outer peripheral surface of the core material 52 and tacky adhesives 54 which adhere the core material 52 and the covering parts 53. The covering parts 53 have the rear surface side covering parts 53a which cover the rear surface 52B and inner peripheral surface 53C of the core material 52 across the tacky adhesives 54 and the front surface covering parts 53b which cover the front surface 52A and inner peripheral surface 52C of the core material 52 across the tacky adhesives 54 and cover the front surface of the rear surface side covering parts 53a.
97 Stabilized methylene chloride JP2753693 1993-01-22 JP3103452B2 2000-10-30 幸男 大歳; 和男 大石
98 Oxazine compounds containing basic groups JP23650585 1985-10-24 JPH0811784B2 1996-02-07 ペドラツツイ ラインハルト
99 Production method of 1,1,1,2-tetrafluoroethane JP29748091 1991-11-13 JPH0780796B2 1995-08-30 アンドレ・ランテ; エリツク・ラクロワ; ベルナール・シユミナル
100 Production of t-butyl chloride JP15197692 1992-06-11 JPH05339180A 1993-12-21 HOTATE MAKOTO; YASHIMA KIMIO
PURPOSE: To quickly produce t-butyl chloride in high yield. CONSTITUTION: t-Butyl alcohol and hydrogen chloride are charged at a molar ratio of 1:(1.1-1.8) into a reaction zone maintained at 60-100°C and made to react with each other in a short contact time of 2-10sec. The reaction proceeds essentially in a state of a vapor-phase contact reaction as a whole. COPYRIGHT: (C)1993,JPO&Japio
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