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公开(公告)号:US5898009A
公开(公告)日:1999-04-27
申请号:US968959
申请日:1997-11-12
Applicant: Gregory W. Shaffer , Richard Frank Hill
Inventor: Gregory W. Shaffer , Richard Frank Hill
IPC: C04B35/5831 , C08K3/38 , C04B35/5833
CPC classification number: C08K3/38 , C01B21/064 , C01B21/0648 , C04B35/5831 , C01P2004/45 , C01P2004/50 , C01P2006/10 , C01P2006/12
Abstract: A method of forming pellets or agglomerates of high density boron nitride from high purity hexagonal boron nitride by crushing the high purity hexagonal boron nitride into boron nitride particles extending over a size range of at least 100 microns with the majority of the particles having a particle size above 50 microns and cold pressing the crushed particles into a compacted form. The compacted form is then granulated into a granulated powder and again cold pressed to form pellets or agglomerates of boron nitride particles with the operations of cold pressing and granulation occurring in one or more stages.
Abstract translation: 通过将高纯度六方氮化硼粉碎至在至少100微米的尺寸范围内延伸的氮化硼颗粒,从高纯度六方氮化硼形成高密度氮化硼的颗粒或附聚物的方法,其中大部分颗粒具有粒径 高于50微米,并将压碎的颗粒冷压成压实形式。 然后将压制形式造粒成造粒粉末,并再次冷压以形成氮化硼颗粒的颗粒或附聚物,其中冷压和造粒的操作在一个或多个阶段中发生。
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公开(公告)号:US5635154A
公开(公告)日:1997-06-03
申请号:US448025
申请日:1995-05-23
Applicant: Kunio Arai , Tadafumi Ajiri
Inventor: Kunio Arai , Tadafumi Ajiri
IPC: C01G49/00 , C01B13/18 , C01B13/32 , C01F1/00 , C01F7/34 , C01G49/06 , C01G49/08 , C01G51/04 , C01G53/04 , C01B13/14 , C01F11/00 , C01G3/02 , C01G49/02
CPC classification number: B82Y30/00 , C01F7/34 , C01G49/06 , C01G51/04 , C01G53/04 , C01P2004/03 , C01P2004/04 , C01P2004/10 , C01P2004/20 , C01P2004/22 , C01P2004/30 , C01P2004/32 , C01P2004/41 , C01P2004/45 , C01P2004/50 , C01P2004/61 , C01P2004/62 , C01P2004/64 , Y02P20/544
Abstract: Disclosed herein is a process for producing fine metal oxide particles comprising the step of heat-treating an aqueous solution of a metal salt at a temperature of not lower than 200.degree. C. under a pressure of not less than 160 kg/cm.sup.2 for 1 second to 1 hour so as to bring into the decomposition reaction of said metal salt.
Abstract translation: 本文公开了一种金属氧化物微粒的制造方法,其特征在于,在不低于160℃/ cm2的压力下,在不低于200℃的温度下对金属盐水溶液进行1秒钟的热处理, 至1小时,以进入所述金属盐的分解反应。
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公开(公告)号:US5480630A
公开(公告)日:1996-01-02
申请号:US714225
申请日:1991-06-12
Applicant: Kunio Arai , Tadafumi Ajiri
Inventor: Kunio Arai , Tadafumi Ajiri
IPC: C01G49/00 , C01B13/18 , C01B13/32 , C01F1/00 , C01F7/34 , C01G49/06 , C01G49/08 , C01G51/04 , C01G53/04 , C01F7/02
CPC classification number: B82Y30/00 , C01F7/34 , C01G49/06 , C01G51/04 , C01G53/04 , C01P2004/03 , C01P2004/04 , C01P2004/10 , C01P2004/20 , C01P2004/22 , C01P2004/30 , C01P2004/32 , C01P2004/41 , C01P2004/45 , C01P2004/50 , C01P2004/61 , C01P2004/62 , C01P2004/64 , Y02P20/544
Abstract: Disclosed herein is a process for producing fine metal oxide particles comprising the step of heat-treating an aqueous solution of a metal salt at a temperature of not lower than 200.degree. C. under a pressure of not less than 160 kg/cm.sup.2 for 1 second to 1 hour so as to bring into the decomposition reaction of said metal salt.
Abstract translation: 本文公开了一种金属氧化物微粒的制造方法,其特征在于,在不低于160℃/ cm2的压力下,在不低于200℃的温度下对金属盐水溶液进行1秒钟的热处理, 至1小时,以进入所述金属盐的分解反应。
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44.
公开(公告)号:US5075269A
公开(公告)日:1991-12-24
申请号:US484283
申请日:1990-02-26
Applicant: Thomas F. Degnan , Ernest W. Valyocsik
Inventor: Thomas F. Degnan , Ernest W. Valyocsik
CPC classification number: B01J29/703 , C01B33/185 , C01B39/48 , C01P2004/03 , C01P2004/20 , C01P2004/45 , C01P2006/80 , C10G2400/10
Abstract: Waxy hydrocarbon oils, e.g., of petroleum origin, are catalytically dewaxed to produce high viscosity index lubricating oil stocks utilizing as catalyst acidic zeolite ZSM-48.
Abstract translation: 将石油来源的蜡质烃油进行催化脱蜡以产生用作催化剂酸性沸石ZSM-48的高粘度指数润滑油原料。
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45.
公开(公告)号:US4888160A
公开(公告)日:1989-12-19
申请号:US47318
申请日:1987-05-08
Applicant: John A. Kosin , Claude R. Andrews
Inventor: John A. Kosin , Claude R. Andrews
IPC: C01F11/18
CPC classification number: C01F11/182 , C01F11/181 , C01P2004/03 , C01P2004/04 , C01P2004/38 , C01P2004/39 , C01P2004/45 , C01P2004/61 , C01P2004/62 , Y10T428/24479
Abstract: A process for producing calcium carbonate from calcium hydroxide derived from, for example, limestone, comprises injecting a gas containing carbon dioxide into a recirculating stream flowing in a recycle piping system in communication with a reaction vessel. The carbon dioxide containing gas is injected at a turbulent area located in the recycle piping system. By controlling reaction parameters including pH and temperature, novel calcium carbonate products are formed by the process.
Abstract translation: 从由例如石灰石衍生的氢氧化钙制备碳酸钙的方法包括将含有二氧化碳的气体注入到与反应容器连通的循环管道系统中流动的再循环流中。 含二氧化碳的气体被注入位于再循环管道系统中的湍流区域。 通过控制包括pH和温度的反应参数,通过该方法形成新的碳酸钙产物。
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46.
公开(公告)号:US20240253989A1
公开(公告)日:2024-08-01
申请号:US18040588
申请日:2021-08-19
Applicant: Denka Company Limited
Inventor: Mana YAMAMOTO , Kenji MIYATA , Yusuke SASAKI
IPC: C01B21/064 , C08K3/38
CPC classification number: C01B21/0648 , C08K3/38 , C01P2002/74 , C01P2004/03 , C01P2004/45 , C01P2006/90 , C08K2003/385 , C08K2201/004
Abstract: A boron nitride particle having a long and thin shape, in which, when the boron nitride particle is subjected to a loading and unloading test comprising a loading step and unloading step in this order, at least a part of a length in the lateral direction of the boron nitride particle compressed in the loading step returns in the unloading step, in which the loading step includes gradually applying a load from 0.2 mN up to 20 mN at a loading rate of 0.27 mN/second in a lateral direction of the boron nitride particle to compress the boron nitride particle, and the unloading step includes gradually unloading the boron nitride particle to 0.2 mN at an unloading rate of 0.27 mN/second.
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公开(公告)号:US20240117193A1
公开(公告)日:2024-04-11
申请号:US18510764
申请日:2023-11-16
Applicant: CarbonX IP 3 B.V.
Inventor: Rutger Alexander David van Raalten , Daniela Sordi
IPC: C09C1/50 , C01B32/00 , C01B32/05 , C01B32/152 , C01B32/158 , C01B32/182
CPC classification number: C09C1/50 , C01B32/00 , C01B32/05 , C01B32/152 , C01B32/158 , C01B32/182 , C01P2004/03 , C01P2004/13 , C01P2004/16 , C01P2004/45 , C01P2006/10 , C01P2006/22 , C01P2006/32 , C01P2006/40
Abstract: The invention pertains to a process for the production of crystalline carbon structure networks in a reactor 3 which contains a reaction zone 3b and a termination zone 3c, by injecting a thermodynamically stable micro-emulsion c, comprising metal catalyst nanoparticles, into the reaction zone 3b which is at a temperature of above 600° C., preferably above 700° C., more preferably above 900° C., even more preferably above 1000° C., more preferably above 1100° C., preferably up to 3000° C., more preferably up to 2500° C., most preferably up to 2000° C., to produce crystalline carbon structure networks e, transferring these networks e to the termination zone 3c, and quenching or stopping the formation of crystalline carbon structure networks in the termination zone by spraying in water d.
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公开(公告)号:US20240109789A1
公开(公告)日:2024-04-04
申请号:US18266839
申请日:2022-02-03
Applicant: LG Chem, Ltd.
Inventor: Ji Hun Jung , Hyun Ah Park , Eung Ju Lee , Min Hee Son
IPC: C01G53/00 , H01M10/052
CPC classification number: C01G53/50 , H01M10/052 , C01P2004/03 , C01P2004/45 , C01P2006/40 , C01P2006/90
Abstract: A positive electrode active material, a method of preparing the same, and a positive electrode and lithium secondary battery including the same are disclosed herein. In some embodiments, a positive electrode active material includes a lithium transition metal oxide which contains 60 mol % or more of nickel based on a total number of moles of transition metals excluding lithium in the lithium transition metal oxide, wherein the oxide is in a form of a secondary particle which is an aggregate of primary particles, wherein the lithium transition metal oxide satisfies Equation 1:
1
≤
x
y
≤
20
Wherein x is a minimum area of a rectangle including all pores having an area greater than 0.002 μm2 among closed pores distributed in the secondary particle, and y is a total sum of areas of the pores having an area greater than 0.002 μm2 among the closed pores distributed in the secondary particle.-
公开(公告)号:US11820667B2
公开(公告)日:2023-11-21
申请号:US16971606
申请日:2019-02-20
Applicant: IMERTECH SAS
Inventor: Nigel V. Jarvis , Graham M. Pring , Desmond Charles Payton , Andrew Findlay , Matthew Cheeseman
CPC classification number: C01F11/183 , C01F11/185 , C09D1/00 , D21H19/385 , D21H21/28 , D21H21/52 , C01P2004/45 , C01P2004/53 , C01P2006/12
Abstract: The present application relates to aqueous slurries comprising precipitated calcium carbonates having a bimodal particle size distribution with a first maximum in particle size distribution and a second maximum in particle size distribution, as well as methods for making them and their uses.
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50.
公开(公告)号:US20230312357A1
公开(公告)日:2023-10-05
申请号:US18044607
申请日:2021-09-10
Applicant: BASF CORPORATION
Inventor: Ming Ming WEI , Shi LIHUA , Vivek VATTIPALLI , Li MENGLU , Liu HAITAO , Li JIN
CPC classification number: C01B39/48 , B01D53/9418 , B01D2257/40 , B01D2255/50 , C01P2004/32 , C01P2004/45
Abstract: Disclosed herein is a process for preparing a zeolite material having an AFX framework structure including X2O3 and YO2 via interzeolite conversion, the process including (1) providing a mixture including a first zeolite material having a non-FAU framework structure including X2O3 and YO2 and an organic structure directing agent selected from the group consisting of diquaternary ammonium cation containing compounds, and (2) heating the mixture from (1) to form a second zeolite material having an AFX framework structure including X2O3 and YO2, wherein X is a trivalent element and Y is a tetravalent element, and where the organic structure directing agent is not 1,4-bis(1,4-diazabicyclo[2.2.2]octane)butyl dihydroxide when the first material zeolite has a CHA framework structure. Further disclosed herein is the zeolite material having an AFX framework structure as obtainable or obtained from the process, and a method of using the same as a catalytically active material.
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