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1. 发明专利

JP2012042480A Method of quasi-continuous chromatograph for separating mixture of two or more multicomponents and corresponding device 有权
标题翻译：用于分离两种或多种多组分和相关装置的混合物的连续色谱法
公开(公告)号：JP2012042480A
公开(公告)日：2012-03-01
申请号：JP2011229759
申请日：2011-10-19
申请人： Bayer Technology Services Gmbh , バイエル・テクノロジー・サービシズ・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング
发明人： ABDELAZIZ TOUMI
IPC分类号： G01N30/46 , G01N30/26
CPC分类号： G01N30/44 , B01D15/1828 , B01D15/1842 , B01D15/1857 , G01N30/463
摘要： PROBLEM TO BE SOLVED: To provide a method of a quasi-continuous chromatograph for separating mixture of two or more multicomponents and a corresponding device.SOLUTION: A device comprising a plurality of individual columns which are coupled to each other in the X direction in a circle is used for performing quasi-continuous processes of a chromatogram for separating the mixture of the two or more multicomponents. Two-dimensional separation is attained by supplying supply liquid, an eluent in the X direction or the Y direction.
摘要翻译：要解决的问题：提供一种用于分离两种或多种多组分混合物的准连续色谱仪和相应的装置。解决方案：包括在X方向上以圆圈彼此连接的多个单独的列的装置用于执行用于分离两个或更多个多组分的混合物的色谱图的准连续过程。通过在X方向或Y方向上供应液体，洗脱液来实现二维分离。版权所有（C）2012，JPO＆INPIT

2. 发明专利

JP2010535823A Preparation of thiophene oligomer 审中-公开
公开(公告)号：JP2010535823A
公开(公告)日：2010-11-25
申请号：JP2010520454
申请日：2008-08-01
申请人：バイエル・テクノロジー・サービシズ・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング
发明人：ヘニンガー，ビヨルン , ムレツコ，レスラウ , ラウシヤー，フランク
IPC分类号： C07D333/28 , C07B61/00
CPC分类号： C08G61/126
摘要： The present invention is based on a process for oligothiophene synthesis at elevated temperatures and low catalyst concentrations.

3. 发明专利

JP2010533058A Thermally stable catalysts for the gas phase oxidation of hydrogen chloride 有权
公开(公告)号：JP2010533058A
公开(公告)日：2010-10-21
申请号：JP2010515372
申请日：2008-06-26
申请人：バイエル・テクノロジー・サービシズ・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング
发明人：シユベルト，シユテフアン , シユリユター，オリバー・フエリクス−カール , ボルフ，アウレル , ムレツコ，レスラウ
IPC分类号： B01J23/63
CPC分类号： B01J23/12 , B01J23/18 , B01J23/22 , B01J23/24 , B01J23/32 , B01J23/63 , B01J23/66 , B01J23/83 , B01J37/0201 , C01B7/04
摘要：本発明は、担体が酸化ウラニウムを含むことを特徴とする、酸化反応の触媒反応において活性な少なくとも１つの成分と、そのための担体を含む、酸化反応のための触媒に関する。この触媒は、安定性および活性が高いことにより注目に値する。
【選択図】なし

4. 发明专利

JP2008542773A Quasi-continuous chromatographic method and a corresponding device for separating a mixture of two or more multicomponent 审中-公开
公开(公告)号：JP2008542773A
公开(公告)日：2008-11-27
申请号：JP2008515116
申请日：2006-06-03
申请人：バイエル・テクノロジー・サービシズ・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング
发明人：トウミ，アブデラジズ
IPC分类号： G01N30/46 , G01N30/26
CPC分类号： G01N30/44 , B01D15/1828 , B01D15/1842 , B01D15/1857 , G01N30/463
摘要：本発明は２成分以上の混合物を分離するための準連続的クロマトグラフの方法と対応する装置に関する。

6. 发明专利

JP2010533114A Production method of chlorine by gas-phase oxidation 审中-公开
公开(公告)号：JP2010533114A
公开(公告)日：2010-10-21
申请号：JP2010515385
申请日：2008-07-01
申请人：バイエル・テクノロジー・サービシズ・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング
发明人：シエレン，ラルフ , シユベルト，シユテフアン , シユリユター，オリバー・フエリクス・カール , ボルフ，アウレル , ムレツコ，レスラウ
IPC分类号： C01B7/04
CPC分类号： B01J8/0496 , B01J8/0438 , B01J8/0453 , B01J8/048 , B01J19/02 , B01J23/12 , B01J2208/00212 , B01J2208/00548 , B01J2208/00557 , B01J2208/00628 , B01J2208/025 , B01J2219/0236 , B01J2219/0277 , B01J2219/0286 , B01J2219/029 , C01B7/04 , F28D9/00 , Y02P20/228
摘要： The present invention relates to a process for preparing chlorine by catalytic gas phase oxidation of hydrogen chloride with oxygen, by reacting the process gas mixture in a reactor in at least two separate reaction zones under adiabatic conditions over catalyst beds, and by passing the process gas mixture leaving at least one reaction zone subsequently through a heat exchanger connected downstream of the particular reaction zone. It further relates to a reactor system for preparing chlorine by catalytic gas phase oxidation of hydrogen chloride with oxygen by means of the process according to the invention.

7. 发明专利

JP2010533059A Catalysts and processes for the production of chlorine by gas-phase oxidation of hydrogen chloride 有权
公开(公告)号：JP2010533059A
公开(公告)日：2010-10-21
申请号：JP2010515386
申请日：2008-07-01
申请人：バイエル・テクノロジー・サービシズ・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング
发明人：シユベルト，シユテフアン , シユリユター，オリバー・フエリクス・カール , ボルフ，アウレル , ムレツコ，レスラウ
IPC分类号： B01J23/12 , B01J23/14 , C01B7/04
CPC分类号： B01J23/12 , B01J23/18 , B01J23/22 , B01J23/24 , B01J23/32 , B01J23/63 , B01J23/66 , B01J23/83 , B01J37/0201 , C01B7/04
摘要：本発明は、塩化水素の接触酸化により塩素を製造するための触媒と、方法に関する。この触媒は、少なくともウラニウムまたはウラニウム化合物を含む活性成分と、担体材料を含む。この触媒は、貴金属と比較して低コストで安定性および活性が高いことにより注目に値する。
【選択図】なし

8. 发明专利

JP5127718B2 Measuring method and use of one or more analytes in a sample of biological origin having a complex composition 有权
公开(公告)号：JP5127718B2
公开(公告)日：2013-01-23
申请号：JP2008536938
申请日：2005-10-29
申请人：バイエル・テクノロジー・サービシズ・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング
发明人：パウラク，ミヒヤエル , シク，エジンハルド , ベントウリ，ミロ , エーラト，マルクス
IPC分类号： G01N33/543 , G01N21/78 , G01N33/553 , G01N37/00
CPC分类号： G01N33/54373 , G01N21/6428 , G01N21/6452 , G01N21/648 , G01N33/54306 , Y10S436/807 , Y10S436/809
摘要： Detection of analytes in biological samples with a complex composition, comprises applying diluted/undiluted samples at discrete places on a solid carrier/after prior application of an adhesive mediation layer on the solid carrier, contacting an array of discrete measuring ranges with a first-, second- and third solution containing binding reagents as specific binding partners for the analytes and optionally in the presence of detection reagents, localized measuring of first-, second- and third optical signals, and recording and comparing of optical signals. The detection of analytes in biological samples with a complex composition, comprises applying diluted/undiluted samples at discrete places on a solid carrier/after prior application of an adhesive mediation layer on the solid carrier, contacting an array of discrete measuring ranges with a first-, second- and third solution containing binding reagents as specific binding partners for the analytes and optionally in the presence of detection reagents, localized measuring of first-, second- and third optical signals, and recording and comparing of optical signals. The binding- and detection reagents are applied at the same time or sequentially. The samples are lysates of cell populations, cell extracts, body fluids and components of body fluids. The measuring range represents a material of less than 1 nL. The detection reagents comprise a polyclonal/monoclonal anti-bodies and antibody fragments, nucleic acids and nucleic acid derivatives and their derivatives with artificial bases, biotin, avidin, streptavidin and neutravidin, and also mass label and/or luminescence label. The labels bind/deposit themselves respectively on/to the binding reagents, on/to the detection reagents or on/to the complexes between the analytes. The binding reagents and optional detection reagents, and/or compounds and/or materials, are pre-incubated with one another and the solutions are brought in contact with the arrays of measuring ranges. A multiplicity of different analytes is detected in a multiplicity of arrays of discrete measuring ranges by addition of the arrays of measuring ranges with different binding reagents. The number of different analytes is equal to the number of various detection reagents, which differ from one another in the excitation and/or emission wavelength of a luminescence. The different binding reagents are applied for the detection of every analyte. A known/different concentrations of compounds are added to the applied material as standards, which are analogous to the analytes. The number of measuring ranges and the extent of the known different concentrations are sufficient to produce a calibration curve to determine the unknown quantity concentrations of the analytes by means of the addition step of a first solution. Many analogous arrays of measuring ranges are arranged on a solid carrier in which the same positions of measuring ranges in different arrays with respect to arrangement in rows and columns. The addition of the samples, measurement- and recordings of the signal take place on different analogous arrays of measuring ranges. The first optical signal produced by non-specific interaction with the reagents is determined from the difference between the optical signals measured after the addition of the second/third solution and the first solution. The concentration/quantity of the analyte is determined from the difference between the measured optical signal and the optical signal produced by non-specific interaction. In the method, less than 10% differences of the concentration of analyte are determined in different samples. The ranges between the measuring ranges are passivated for the minimization of non-specific binding of reagents, in which non-binding chemically neutral components are applied between the spatially separated measuring ranges with respect to the mentioned binding reagents and/or detection reagents. The solid carrier is optically transparent to an irradiated excitation light/measuring light and has microscope plates, micro-titer plates, nano-titer plates, filters, membranes, micro-structured carriers, and a single- or multi-layered optical wave guide that is continuous or divided into discrete wave-guiding ranges. The excitation or measuring light of polychromatic or monochromatic sources of light is led to measuring ranges of the arrays and optical signals from the measuring ranges and/or changes or differences of the optical signals from the measuring ranges are measured in a localized manner and recorded. Independent claims are included for: (1) a micro array for quantitative regulation of analytes in samples of biological origin; and (2) a procedure for the quantitative regulation of analytes in samples of biological origin.

9. 发明专利

JP5033794B2 Time-controlled intravenous administration devices anesthetic propofol 有权
公开(公告)号：JP5033794B2
公开(公告)日：2012-09-26
申请号：JP2008516175
申请日：2006-06-03
申请人：バイエル・テクノロジー・サービシズ・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング
发明人：エジントン，アンドレア・ニコル , シユミツト，バルター , ビルマン，シユテフアン
IPC分类号： A61M5/00 , G06F19/00
CPC分类号： A61M5/1723 , G06F19/3481 , G16H50/50
摘要： The invention relates to a device for the time-controlled intravenous administering of the anesthetic propofol by means of a method used for determining an adequate dosage profile and adequately controlling an infusion pump as a metering apparatus.

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