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1. 发明申请

US20070292331A1 Microporous crystals and synthesis schemes 失效
标题翻译：微孔晶体和合成方案
公开(公告)号：US20070292331A1
公开(公告)日：2007-12-20
申请号：US11206330
申请日：2005-08-17
申请人： William Tumas , Kevin Ott , T. McCleskey , Matthew Yates , Eva Birnbaum
发明人： William Tumas , Kevin Ott , T. McCleskey , Matthew Yates , Eva Birnbaum
IPC分类号： B01J27/00
CPC分类号： C01B37/04 , C01B39/54 , Y10S423/30
摘要： Novel zeolites are produced by combining a polar solute, a silicon or phosphorous source, and a structure directing agent. Surfactants and a hydrophobic solvent are added to the previously mixed three species and shaken to disperse the surfactants. The reverse microemulsion is stirred overnight, at about room temperature and then iced for five to ten minutes. A metal source is added vigorously shaken for about two minutes. The mixture is then aged for about two hours at about room temperature. A mineralizer is added and the resultant mixture aged for about two hours at about room temperature. The mixture is heated to about 180° C., for a suitable time period. The final novel product is then isolated.
摘要翻译：通过组合极性溶质，硅或磷源和结构导向剂来制备新型沸石。将表面活性剂和疏水性溶剂加入到先前混合的三种物质中并摇动以分散表面活性剂。将反相微乳液在约室温下搅拌过夜，然后冰化5至10分钟。将金属源剧烈振动约两分钟。然后将混合物在约室温下老化约2小时。加入矿化剂，所得混合物在约室温下老化约2小时。将混合物加热至约180℃，持续合适的时间。然后分离最终的新产品。

2. 发明申请

US20080011956A1 Nanophosphors for large area radiation detectors 失效
标题翻译：用于大面积辐射探测器的纳米荧光粉
公开(公告)号：US20080011956A1
公开(公告)日：2008-01-17
申请号：US11729279
申请日：2007-03-27
申请人： Anthony Burrell , Kevin Ott , John Gordon , Rico Del Sesto , T. McCleskey
发明人： Anthony Burrell , Kevin Ott , John Gordon , Rico Del Sesto , T. McCleskey
IPC分类号： G01T1/20 , C09K11/85
CPC分类号： G01T1/202 , C09K11/7774 , G01T1/2018 , Y10S977/773 , Y10S977/776 , Y10S977/832
摘要： Nanophosphor compositions were was prepared. The compositions can be used for radiation detection.
摘要翻译：制备纳米荧光体组合物。组合物可用于辐射检测。

3. 发明申请

US20060029535A1 Catalyst and method for reduction of nitrogen oxides 失效
标题翻译：用于还原氮氧化物的催化剂和方法
公开(公告)号：US20060029535A1
公开(公告)日：2006-02-09
申请号：US10899749
申请日：2004-07-27
申请人： Kevin Ott
发明人： Kevin Ott
IPC分类号： B01D53/56
CPC分类号： B01J29/7615 , B01D53/8625 , Y02C20/10
摘要： A Selective Catalytic Reduction (SCR) catalyst was prepared by slurry coating ZSM-5 zeolite onto a cordierite monolith, then subliming an iron salt onto the zeolite, calcining the monolith, and then dipping the monolith either into an aqueous solution of manganese nitrate and cerium nitrate and then calcining, or by similar treatment with separate solutions of manganese nitrate and cerium nitrate. The supported catalyst containing iron, manganese, and cerium showed 80 percent conversion at 113 degrees Celsius of a feed gas containing nitrogen oxides having 4 parts NO to one part NO2, about one equivalent ammonia, and excess oxygen; conversion improved to 94 percent at 147 degrees Celsius. N2O was not detected (detection limit: 0.6 percent N2O).
摘要翻译：通过将ZSM-5沸石浆料涂布到堇青石整料上制备选择性催化还原（SCR）催化剂，然后将铁盐升华到沸石上，煅烧整料，然后将整料浸入硝酸锰和铈的水溶液中硝酸盐，然后煅烧，或通过用硝酸锰和硝酸铈的单独溶液进行类似处理。含有铁，锰和铈的载体催化剂在113摄氏度的含有氮氧化物的转化率为80％，所述氮氧化物含有4份NO至1份NO 2，约1当量氨和过量氧 ; 转化率在147摄氏度时提高到94％。未检测到N 2 O（检测限：0.6％N 2 O）。

4. 发明申请

US20060159607A1 Catalyst and method for reduction of nitrogen oxides 失效
公开(公告)号：US20060159607A1
公开(公告)日：2006-07-20
申请号：US11385140
申请日：2006-03-20
申请人： Kevin Ott
发明人： Kevin Ott
IPC分类号： B01J29/04 , B01J29/87 , B01J29/06 , B01D53/86 , B01J8/00
CPC分类号： B01D53/9418 , B01D53/8628 , B01D2251/2062 , B01D2255/2065 , B01D2255/2073 , B01D2255/20738 , B01D2255/50 , B01D2255/504 , B01J29/076 , B01J29/46 , B01J29/48 , B01J35/0006 , B01J37/0246 , Y02C20/10
摘要： A Selective Catalytic Reduction (SCR) catalyst was prepared by slurry coating ZSM-5 zeolite onto a cordierite monolith, then subliming an iron salt onto the zeolite, calcining the monolith, and then dipping the monolith either into an aqueous solution of manganese nitrate and cerium nitrate and then calcining, or by similar treatment with separate solutions of manganese nitrate and cerium nitrate. The supported catalyst containing iron, manganese, and cerium showed 80 percent conversion at 113 degrees Celsius of a feed gas containing nitrogen oxides having 4 parts NO to one part NO2, about one equivalent ammonia, and excess oxygen; conversion improved to 94 percent at 147 degrees Celsius. N2O was not detected (detection limit: 0.6 percent N2O).

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