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公开(公告)号：US20090291039A1
公开(公告)日：2009-11-26
申请号：US12431496
申请日：2009-04-28
IPC分类号： C01B35/14
CPC分类号： C01B35/146 , C01B3/001 , C01B35/14 , Y02E60/324
摘要： The present invention discloses new methods for synthesizing ammonia borane (NH3BH3, or AB). Ammonium borohydride (NH4BH4) is formed from the reaction of borohydride salts and ammonium salts in liquid ammonia. Ammonium borohydride is decomposed in an ether-based solvent that yields AB at a near quantitative yield. The AB product shows promise as a chemical hydrogen storage material for fuel cell powered applications.
摘要翻译： 本发明公开了合成氨硼烷（NH3BH3或AB）的新方法。 硼氢化钠（NH4BH4）由硼氢化物盐和铵盐在液氨中的反应形成。 硼氢化钠在基于醚的溶剂中分解，其产率接近于定量。 AB产品显示了作为燃料电池供电应用的化学储氢材料的前景。
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公开(公告)号：US07897129B2
公开(公告)日：2011-03-01
申请号：US12431496
申请日：2009-04-28
IPC分类号： C01B35/14
CPC分类号： C01B35/146 , C01B3/001 , C01B35/14 , Y02E60/324
摘要： The present invention discloses new methods for synthesizing ammonia borane (NH3BH3, or AB). Ammonium borohydride (NH4BH4) is formed from the reaction of borohydride salts and ammonium salts in liquid ammonia. Ammonium borohydride is decomposed in an ether-based solvent that yields AB at a near quantitative yield. The AB product shows promise as a chemical hydrogen storage material for fuel cell powered applications.
摘要翻译： 本发明公开了合成氨硼烷（NH3BH3或AB）的新方法。 硼氢化钠（NH4BH4）由硼氢化物盐和铵盐在液氨中的反应形成。 硼氢化钠在基于醚的溶剂中分解，其产率接近于定量。 AB产品显示了作为燃料电池供电应用的化学储氢材料的前景。
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3.发明授权System and process for capture of acid gasses at elevated pressure from gaseous process streams 有权用于从气态工艺流高压捕获酸性气体的系统和方法公开(公告)号：US09433892B2
公开(公告)日：2016-09-06
申请号：US14516900
申请日：2014-10-17
申请人： David J. Heldebrant , Phillip K. Koech , John C. Linehan , James E. Rainbolt , Mark D. Bearden , Feng Zheng
发明人： David J. Heldebrant , Phillip K. Koech , John C. Linehan , James E. Rainbolt , Mark D. Bearden , Feng Zheng
CPC分类号： B01D53/40 , B01D53/1475 , B01D53/1493 , B01D53/77 , B01D53/78 , B01D2252/20431 , B01D2252/30 , B01D2252/40 , B01D2257/504 , Y02C10/06
摘要： A system, method, and material that enables the pressure-activated reversible chemical capture of acid gasses such as CO2 from gas volumes such as streams, flows or any other volume. Once the acid gas is chemically captured, the resulting product typically a zwitterionic salt, can be subjected to a reduced pressure whereupon the resulting product will release the captures acid gas and the capture material will be regenerated. The invention includes this process as well as the materials and systems for carrying out and enabling this process.
摘要翻译： 一种系统，方法和材料，其能够从诸如流，流或任何其它体积的气体体积进行压力激活的可逆化学捕获酸性气体（例如CO 2）。 一旦酸性气体被化学捕获，所得到的产物通常是两性离子盐，可以经受减压，于是所得产物将释放捕获的酸性气体并且捕获材料将被再生。 本发明包括该过程以及用于执行和实现该过程的材料和系统。
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4.发明申请SYSTEM AND PROCESS FOR CAPTURE OF ACID GASSES AT ELEVATED-PRESSURE FROM GASEOUS PROCESS STREAMS 审中-公开从气体过程流中获取高压酸的酸度的系统和方法公开(公告)号：US20120061613A1
公开(公告)日：2012-03-15
申请号：US12879579
申请日：2010-09-10
申请人： David J. Heldebrant , Phillip K. Koech , John C. Linehan , James E. Rainbolt , Mark D. Bearden , Feng Zheng
发明人： David J. Heldebrant , Phillip K. Koech , John C. Linehan , James E. Rainbolt , Mark D. Bearden , Feng Zheng
IPC分类号： C07C69/96 , C09K3/00 , C07C215/08
CPC分类号： B01D53/40 , B01D53/1475 , B01D53/1493 , B01D53/77 , B01D53/78 , B01D2252/20431 , B01D2252/30 , B01D2252/40 , B01D2257/504 , Y02C10/06
摘要： A system, method, and material that enables the pressure-activated reversible chemical capture of acid gasses such as CO2 from gas volumes such as streams, flows or any other volume. Once the acid gas is chemically captured, the resulting product typically a zwitterionic salt, can be subjected to a reduced pressure whereupon the resulting product will release the captures acid gas and the capture material will be regenerated. The invention includes this process as well as the materials and systems for carrying out and enabling this process.
摘要翻译： 一种系统，方法和材料，其能够从诸如流，流或任何其它体积的气体体积进行压力激活的可逆化学捕获酸性气体（例如CO 2）。 一旦酸性气体被化学捕获，所得到的产物通常是两性离子盐，可以经受减压，于是所得产物将释放捕获的酸性气体，捕获材料将被再生。 本发明包括该过程以及用于执行和实现该过程的材料和系统。
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5.发明申请SYSTEM AND PROCESS FOR CAPTURE OF ACID GASSES AT ELEVATED PRESSURE FROM GASEOUS PROCESS STREAMS 审中-公开从气体过程流中获取高压酸的酸度的系统和方法公开(公告)号：US20150050203A1
公开(公告)日：2015-02-19
申请号：US14516900
申请日：2014-10-17
申请人： David J. Heldebrant , Phillip K. Koech , John C. Linehan , James E. Rainbolt , Mark D. Bearden , Feng Zheng
发明人： David J. Heldebrant , Phillip K. Koech , John C. Linehan , James E. Rainbolt , Mark D. Bearden , Feng Zheng
CPC分类号： B01D53/40 , B01D53/1475 , B01D53/1493 , B01D53/77 , B01D53/78 , B01D2252/20431 , B01D2252/30 , B01D2252/40 , B01D2257/504 , Y02C10/06
摘要： A system, method, and material that enables the pressure-activated reversible chemical capture of acid gasses such as CO2 from gas volumes such as streams, flows or any other volume. Once the acid gas is chemically captured, the resulting product typically a zwitterionic salt, can be subjected to a reduced pressure whereupon the resulting product will release the captures acid gas and the capture material will be regenerated. The invention includes this process as well as the materials and systems for carrying out and enabling this process.
摘要翻译： 一种系统，方法和材料，其能够从诸如流，流或任何其它体积的气体体积进行压力激活的可逆化学捕获酸性气体（例如CO 2）。 一旦酸性气体被化学捕获，所得到的产物通常是两性离子盐，可以经受减压，于是所得产物将释放捕获的酸性气体，捕获材料将被再生。 本发明包括该过程以及用于执行和实现该过程的材料和系统。
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6.发明授权Process of forming compounds using reverse micelle or reverse microemulsion systems 失效使用反胶束或反相微乳液体系形成化合物的方法
公开(公告)号：US5770172A
公开(公告)日：1998-06-23
申请号：US725840
申请日：1996-10-04
申请人： John C. Linehan , John L. Fulton , Roger M. Bean
发明人： John C. Linehan , John L. Fulton , Roger M. Bean
IPC分类号： B01J19/00 , C01B13/32 , C01G49/00 , C01G49/06 , C01G49/08 , C01G49/12 , C10G1/08 , C01G49/02
CPC分类号： B82Y30/00 , B01J35/0013 , C01B13/328 , C01G49/009 , C01G49/06 , C01G49/08 , C01G49/12 , C10G1/086 , C01P2004/64
摘要： The present invention is directed to a process for producing a nanometer-sized metal compound. The process comprises forming a reverse micelle or reverse microemulsion system comprising a polar fluid in a non-polar or low-polarity fluid. A first reactant comprising a multi-component, water-soluble metal compound is introduced into the polar fluid in a non-polar or low-polarity fluid. This first reactant can be introduced into the reverse micelle or reverse microemulsion system during formation thereof or subsequent to the formation of the reverse micelle or microemulsion system. The water-soluble metal compound is then reacted in the reverse micelle or reverse microemulsion system to form the nanometer-sized metal compound. The nanometer-sized metal compound is then precipitated from the reverse micelle or reverse microemulsion system.
摘要翻译： 本发明涉及一种制备纳米尺寸金属化合物的方法。 该方法包括形成非极性或低极性流体中包含极性流体的反胶束或反相微乳液体系。 将包含多组分水溶性金属化合物的第一反应物以非极性或低极性流体引入极性流体中。 该第一反应物可以在其形成期间或在形成反胶束或微乳液体系之后引入反胶束或反相微乳液体系中。 然后将水溶性金属化合物在反胶束或反相微乳液体系中反应形成纳米级金属化合物。 然后将纳米级金属化合物从反胶束或反相微乳液体系中沉淀出来。
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公开(公告)号：US5652192A
公开(公告)日：1997-07-29
申请号：US412480
申请日：1995-03-28
申请人： Dean W. Matson , John L. Fulton , John C. Linehan , Roger M. Bean , Thomas D. Brewer , Todd A. Werpy , John G. Darab
发明人： Dean W. Matson , John L. Fulton , John C. Linehan , Roger M. Bean , Thomas D. Brewer , Todd A. Werpy , John G. Darab
IPC分类号： B01J3/00 , B01J35/00 , B22F1/02 , B22F9/24 , B22F9/30 , C01B13/32 , C01B13/36 , C01B17/20 , B01J23/10 , B01J23/44 , B01J27/053 , C22B5/20
CPC分类号： B82Y30/00 , B01J3/00 , B01J35/0013 , B22F1/025 , B22F9/24 , B22F9/30 , C01B13/32 , C01B13/366 , C01B17/20 , B22F2998/00 , C01P2002/60 , C01P2002/72 , C01P2004/03 , C01P2004/52 , C01P2004/54 , C01P2004/61 , C01P2004/62 , C01P2004/64 , C01P2006/12 , Y10S505/733
摘要： The material of the present invention is a mixture of catalytically active material and carrier materials, which may be catalytically active themselves. Hence, the material of the present invention provides a catalyst particle that has catalytically active material throughout its bulk volume as well as on its surface. The presence of the catalytically active material throughout the bulk volume is achieved by chemical combination of catalytically active materials with carrier materials prior to or simultaneously with crystallite formation.
摘要翻译： 本发明的材料是催化活性材料和载体材料的混合物，它们本身可具有催化活性。 因此，本发明的材料提供了催化剂颗粒，其整个整体体积以及其表面都具有催化活性材料。 在整个体积体积中催化活性材料的存在通过在微晶形成之前或同时与催化活性材料与载体材料的化学组合来实现。
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公开(公告)号：US5469061A
公开(公告)日：1995-11-21
申请号：US42351
申请日：1993-04-02
CPC分类号： G01N21/05 , G01R33/30 , G01N2021/0346 , G01R33/307
摘要： The present invention is an arrangement of a glass capillary tube for use in spectroscopy. In particular, the invention is a capillary arranged in a manner permitting a plurality or multiplicity of passes of a sample material through a spectroscopic measurement zone. In a preferred embodiment, the multi-pass capillary is insertable within a standard NMR sample tube. The present invention further includes a method of making the multi-pass capillary tube and an apparatus for spinning the tube.
摘要翻译： 本发明是用于光谱学的玻璃毛细管的布置。 特别地，本发明是以允许样品材料通过光谱测量区域的多次或多次通过的方式布置的毛细管。 在优选实施例中，多通毛细管可插入标准NMR样品管内。 本发明还包括制造多通毛细管的方法和用于纺丝管的装置。
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9.发明授权公开(公告)号：US11021661B2
公开(公告)日：2021-06-01
申请号：US13401216
申请日：2012-02-21
申请人： James J. Strohm , John C. Linehan , Benjamin Q. Roberts , Douglas L. McMakin , David M. Sheen , Jeffrey W. Griffin , James A. Franz , Charlene Franz
发明人： James J. Strohm , John C. Linehan , Benjamin Q. Roberts , Douglas L. McMakin , David M. Sheen , Jeffrey W. Griffin , James A. Franz
IPC分类号： C10G32/02 , B01J19/12 , H05H1/46 , B01J19/00 , B01J19/08 , C10G9/24 , C10G1/02 , C10G1/00 , C10G1/08 , C10G15/08
摘要： Conversion of heavy fossil hydrocarbons (HFH) to a variety of value-added chemicals and/or fuels can be enhanced using microwave (MW) and/or radio-frequency (RF) energy. Variations of reactants, process parameters, and reactor design can significantly influence the relative distribution of chemicals and fuels generated as the product. In one example, a system for flash microwave conversion of HFH includes a source concentrating microwave or RF energy in a reaction zone having a pressure greater than 0.9 atm, a continuous feed having HFH and a process gas passing through the reaction zone, a HFH-to-liquids catalyst contacting the HFH in at least the reaction zone, and dielectric discharges within the reaction zone. The HFH and the catalyst have a residence time in the reaction zone of less than 30 seconds. In some instances, a plasma can form in or near the reaction zone.
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