| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 1 | 金属络合物和过氧化氢的制造方法 | CN201380048834.3 | 2013-08-02 | CN104640854B | 2016-08-24 | 小江诚司; 加藤贤治; 长田昌辉 |
| 本发明的目的在于，提供能够替代以往的蒽醌法的、新型的过氧化氢的基于直接合成的制造方法以及该制造方法中使用的催化剂。本发明为下述通式(1)、(2)、(3)或(4)所示的金属络合物。 | ||||||
| 2 | 在自动氧化过氧化氢生产中回收水性过氧化氢 | CN200880008163.7 | 2008-03-14 | CN101631743A | 2010-01-20 | X·周; K·哈马克; D·S·塞斯 |
| 在具有小截面尺寸的长通道的装置中，用水性介质通过液-液萃取从含H<sub>2</sub>O<sub>2</sub>的有机溶液中回收自动氧化方法中产生的过氧化氢，所述通道有利于从有机溶液中有效萃取水性过氧化氢。 | ||||||
| 3 | 过氧化氢的制备方法 | CN93114940.1 | 1993-11-20 | CN1087600A | 1994-06-08 | 平山秀二; 广本和彦; 门前博之; 近藤信幸; 石上春树; 石村善正 |
| 在反应介质中，通过氢和氧接触制造过氧化氢的方法中，使用在铌氧化物、铌复合氧化物、钽氧化物、钽复合氧化物、钼氧化物，或钨氧化物上载持有铂族金属的铂族金属催化剂。 | ||||||
| 4 | 纳米氧化铜模拟半胱氨酸氧化酶 | CN201710157957.0 | 2017-03-16 | CN106955704A | 2017-07-18 | 陈伟; 胡爱玲; 邓豪华; 彭花萍; 林秀玲 |
| 本发明公开一种纳米氧化铜模拟半胱氨酸氧化酶，所述的纳米氧化铜是以快速沉淀法制备得到。纳米氧化铜具有优良的半胱氨酸氧化酶活性，可催化氧气氧化半胱氨酸生成胱氨酸和过氧化氢。可用于将半胱氨酸快速转化为胱氨酸、将氧气转化为过氧化氢等。本发明所使用的纳米氧化铜制备过程简单快速。本发明纳米氧化铜模拟半胱氨酸氧化酶，可实现半胱氨酸快速转化为胱氨酸以及氧气快速转化为过氧化氢。 | ||||||
| 5 | 金属络合物和过氧化氢的制造方法 | CN201380048834.3 | 2013-08-02 | CN104640854A | 2015-05-20 | 小江诚司; 加藤贤治; 长田昌辉 |
| 本发明的目的在于，提供能够替代以往的蒽醌法的、新型的过氧化氢的基于直接合成的制造方法以及该制造方法中使用的催化剂。本发明为下述通式(1)、(2)、(3)或(4)所示的金属络合物。 | ||||||
| 6 | 在自动氧化过氧化氢生产中回收水性过氧化氢 | CN200880008163.7 | 2008-03-14 | CN101631743B | 2014-10-01 | X·周; K·哈马克; D·S·塞斯 |
| 在具有小截面尺寸的长通道的装置中，用水性介质通过液-液萃取从含H2O2的有机溶液中回收自动氧化方法中产生的过氧化氢，所述通道有利于从有机溶液中有效萃取水性过氧化氢。 | ||||||
| 7 | 利用光过氧化方法的聚合物组合物和聚合引发剂 | CN200980153851.7 | 2009-12-21 | CN102264837A | 2011-11-30 | O·卡巴舍斯库 |
| 本发明公开了一种橡胶改性聚合物组合物，其主要具有核-壳形态。所述橡胶改性聚合物组合物可以是包含苯乙烯、聚丁二烯和高接枝引发剂的聚苯乙烯，其中高接枝引发剂通过使单重态氧接触包含烯丙氢或二烯的烯烃，形成氢过氧化物或过氧化物来形成。所述单重态氧可通过使基态氧接触光催化剂形成，如曝光的光敏染料。 | ||||||
| 8 | 过氧化氢的制备方法 | CN93114940.1 | 1993-11-20 | CN1035320C | 1997-07-02 | 平山秀二; 广本和彦; 门前博之; 近藤信幸; 石上春树; 石村善正 |
| 在反应介质中，通过氢和氧接触制造过氧化氢的方法中，使用在铌氧物、铌复合氧化物、钽氧化物、钽复合氧化物、钼氧化物，或钨氧化物上载持有铂族金属的铂族金属催化剂。 | ||||||
| 9 | 金属錯体及び過酸化水素の製造方法 | JP2012205229 | 2012-09-19 | JP6063681B2 | 2017-01-18 | 小江 誠司; 加藤 賢治; 長田 昌輝 |
| 10 | Recovery of aqueous hydrogen peroxide in the auto-oxidation h2o2 manufacturing | JP2009553812 | 2008-03-14 | JP2010521398A | 2010-06-24 | エス セチ，ダルビール; チョー，シンリャン; ハムマック，ケビン |
| 約５ミクロンから約５ｍｍの範囲内の少なくとも１つの断面の大きさを有する長いチャンネルをもつ装置中で自動酸化プロセス例えばアントラキノン自動酸化におけるＨ
２ Ｏ
２含有有機溶液と水性抽出媒体とを接触させて有機溶液から水性媒体への過酸化水素の液体−液体抽出を行い、次にＨ
２ Ｏ
２の減少した有機溶液から抽出された過酸化水素を含む水性媒体を分離してＨ
２ Ｏ
２含有水溶液を得る自動酸化プロセスで生成された過酸化水素を回収する方法であって、抽出による物質移動で従来のシーブトレーカラムよりも能率的であり、しかもこのようなカラムよりもコストが低い抽出装置において、過酸化水素含有有機溶液から水性過酸化水素の液体−液体抽出を行う改善された方法の提供。
【選択図】図１ |
||||||
| 11 | Direct manufacturing method of hydrogen peroxide | JP27851598 | 1998-09-30 | JP3382860B2 | 2003-03-04 | イン リー ウォー; エオン パルク サン; ウェー リー チュール; ワー ヨー ユン; キ パルク ヨン; サン チャン ヨン |
| 12 | PORTABLE CHEMICAL OXYGEN GENERATOR | US15811148 | 2017-11-13 | US20180154192A1 | 2018-06-07 | Richard P. Imbruce; David Cowan |
| A portable chemical oxygen generator for delivering oxygen to a patient is described. The generator includes a housing containing a reaction chamber. Within the reaction chamber is a quantity of a peroxide adduct. A valve is provided with a lower portion of the valve in fluid communication with the reaction chamber. An upper portion of the valve is in fluid communication with a reservoir that holds a quantity of an aqueous solution. An internal chamber is formed within the valve by releasable seals that separate the internal chamber from the upper portion of the valve and a lower portion of the valve. The internal chamber holds a quantity of a peroxide-decomposing catalyst. The generator also includes a valve actuator. Operation of the valve actuator releases the seals in the valve and creates a fluid path from the reservoir through the internal chamber into the reaction chamber. When the valve is actuated, the aqueous solution flows from the reservoir through the internal chamber and into the reaction chamber. This flow washes the catalyst into the reaction chamber along with the aqueous solution. The solution and catalyst mix with the peroxide adduct and cause an oxygen-generating reaction. | ||||||
| 13 | Portable chemical oxygen generator | US15366891 | 2016-12-01 | US09849312B1 | 2017-12-26 | Richard P. Imbruce; David Cowan |
| A portable chemical oxygen generator for delivering oxygen to a patient is described. The generator includes a housing containing a reaction chamber. Within the reaction chamber is a quantity of a peroxide adduct. A valve is provided with a lower portion of the valve in fluid communication with the reaction chamber. An upper portion of the valve is in fluid communication with a reservoir that holds a quantity of an aqueous solution. An internal chamber is formed within the valve by releasable seals that separate the internal chamber from the upper portion of the valve and a lower portion of the valve. The internal chamber holds a quantity of a peroxide-decomposing catalyst. The generator also includes a valve actuator. Operation of the valve actuator releases the seals in the valve and creates a fluid path from the reservoir through the internal chamber into the reaction chamber. When the valve is actuated, the aqueous solution flows from the reservoir through the internal chamber and into the reaction chamber. This flow washes the catalyst into the reaction chamber along with the aqueous solution. The solution and catalyst mix with the peroxide adduct and cause an oxygen-generating reaction. | ||||||
| 14 | Chemical process | US11476894 | 2006-06-29 | US20070012579A1 | 2007-01-18 | Magnus Rosvall; Rolf Edvinsson Albers |
| The invention relates to a process for the production of alkali metal chlorate comprising: providing an electrochemical cell comprising an anode and a cathode in separate anode and cathode compartments; contacting the cathode with an electrolyte comprising at least one organic mediator and one or more organic or mineral acids; reacting the organic mediator at the cathode to form at least one reduced form of the mediator; reacting the at least one reduced form of the mediator with oxygen to form hydrogen peroxide; contacting the anode with an anolyte comprising alkali metal chloride; reacting chloride at the anode to form chlorine that is hydrolysed; and, reacting the hydrolysed chlorine to form chlorate. | ||||||
| 15 | Agents and methods for generation of active oxygen | US700592 | 1996-08-14 | US5741887A | 1998-04-21 | Ken-ichi Morita; Shigeru Otsuka; Kiyoshi Saito |
| Agents containing polyaniline of one or more specified kinds shown by Formulas (1)-(4) given below can generate active oxygen efficiently and economically when contacted with a liquid having oxygen dissolved therein: ##STR1## where A is a negative ion, n is an integer between 2 and 5000, x and y are numbers such that x+y=1 and 0.ltoreq.y.ltoreq.0.5. | ||||||
| 16 | Photochemical production of hydrogen peroxide | US402463 | 1989-09-05 | US4946566A | 1990-08-07 | R. D. Samuel Stevens; Stephen R. Cater; Clarke E. Slemon |
| The present invention relates to a photochemical process for the manufacture of hydrogen peroxidewherein a 9,10-phenanthraquinone compound is exposed, in the presence of an effective amount of a hydrogen donor alcohol, to electromagnetic radiation to photoreduce the 9,10-phenanthraquinone compound to the correpsonding dihydro-compound,wherein the dihydro-compound obtained is oxidized to produce hydrogen peroxide and to regenerate the 9,10-phenanthraquinone compound, andcharacterized in that said 9,10-phenanthraquinone compound is selected from the group of compounds consisting of unsubstituted 9,10-phenanthraquinone and 9,10-phenanthraquinone substituted by one or more members of the class consisting of alkyl groups of 1 to 8 carbon atoms, --CF.sub.3, F and --SO.sub.3 M, M being H or an alkali metal. | ||||||
| 17 | Process for preparing hydrogen peroxide | US547193 | 1983-10-31 | US4547354A | 1985-10-15 | Frances S. Pinault |
| An improved process for the acid-catalyzed hydrolysis tertiary butyl hydroperoxide to form hydrogen peroxide wherein an organic solvent is added to the hydrolysis zone, which solvent promotes the partitioning of hydrogen peroxide and oxidizable organic material into separate aqueous and organic phases, respectively. | ||||||
| 18 | Metal cage complexes and production thereof | US355663 | 1982-03-08 | US4497737A | 1985-02-05 | Alan M. Sargeson; Anthony J. Herlt; John M. Harrowfield |
| Hydrogen peroxide is produced by oxidation of a coordination complex of a metal ion capable of existing in at least two oxidation states and a ligand, the coordination complex being sufficiently stable for the metal ion to be oxidized and reduced without decomposition of the complex and the metal ion being in its lower oxidation state. In a cyclic process, the step of reduction of the complex with the metal ion in its higher oxidation state precedes the oxidation step, and the reduction and oxidation steps are repeated sequentially. Novel coordination complexes which may be used in the process have the formula: ##STR1## in which n represents an integer; M represents a cobalt ion or other metal ion having at least two oxidation states; x and y, which may be the same or different, each represent .tbd.N, .tbd.P or .tbd.C--R', in which R' represents a hydrogen or halogen atom, or a hydroxyl, nitro, nitroso, amino, alkyl, or cyano group, or a group of the formula --COOR", --COCOOR" or --NH--COCH--CHCOOR" in which R" is a hydrogen atom or alkyl group; provided that when M represents a cobalt ion and n is 2, x and y do not both represent .tbd.N. | ||||||
| 19 | Polymer composition and the polymerization initiator using light peroxidation process | JP2011543608 | 2009-12-21 | JP2012514079A | 2012-06-21 | カバシエスク，オルガ |
| A rubber-modified polymeric composition having predominately core-shell morphology is disclosed. The rubber-modified polymeric composition can be a polystyrene comprising styrene, polybutadiene, and a high-grafting initiator formed by contacting singlet oxygen with an olefin containing an allylic hydrogen or a diene to form a hydroperoxide or peroxide. The singlet oxygen can be formed by contacting ground state oxygen with a photo catalyst, such a photosensitive dye exposed to light. | ||||||
| 20 | Method for producing hydrogen peroxide | JP51296494 | 1993-11-16 | JP3394043B2 | 2003-04-07 | 秀二 平山; 和彦 広本; 春樹 石上; 善正 石村; 信幸 近藤; 博之 門前 |
QQ群二维码
意见反馈
意见反馈