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水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 |