子分类：
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 41 | 圧電磁器組成物及びその製造方法 | JP2012547394 | 2012-03-02 | JPWO2013128651A1 | 2015-07-30 | 流田 賢治; 賢治 流田; 敦灼 薫 |
| 【課題】良好な圧電特性を有しかつ特性バラツキが少ない圧電磁器組成物を提供すること。【解決手段】圧電磁器組成物10は、組成式ABO3で表されるペロブスカイト構造の結晶相を主相として含む。A元素は、K,Na,Liから選択される1つ以上の元素であり、B元素は、Nb,Ta,Sbから選択される1つ以上の元素である。圧電磁器組成物10には、A元素及びB元素とは異なる他の元素が添加されている。圧電磁器組成物10の粉末試料のX線回折プロファイルにおいて、主相と、組成式AsBtOu(s | ||||||
| 42 | 安定な酸素終端半導体ナノ粒子の製造方法 | JP2011508013 | 2009-04-09 | JP5650103B2 | 2015-01-07 | デイビッド・トーマス・ブリトン; マルギット・ヘルティング |
| 43 | Electrode active material and a method of manufacturing the same for a secondary battery | JP2011537364 | 2009-11-20 | JP2012509564A | 2012-04-19 | ウーム、インスン; オー、ビュン、フン; キム、ジェヤン; クウォン、ウジュン; チェ、スンユン; リー、ヨンジュ |
| 本発明は、（ａ）リチウムと合金化が可能な（準）金属の酸化物からなる第１粒子相；及び（ｂ）前記（準）金属と同一の（準）金属及びリチウムを同時に含有する酸化物からなる第２粒子相を含むことが特徴である電極活物質、及びこのような電極活物質を含む二次電池に関する。 本発明に係る電極活物質は、アノード活物質に用いるとき、電池の初期充／放電以前に既に前記第２粒子相内にリチウムが含有されているので、電池の初期充／放電時にリチウム酸化物やリチウムメタル酸化物のような非可逆相がより少なく生成され、これによりカソード側のデッドボリューム（dead volume）が最小化できるので、高容量の電池が製造可能である。 | ||||||
| 44 | Nanoparticles and methods for their preparation with a rutile-like crystalline phase | JP2003547308 | 2002-09-16 | JP4276077B2 | 2009-06-10 | エス． アーニー，デイビッド; ジェイ．ザ フォース スタディナー，チャールズ; エー． ヒギンス，ジェイムズ; ダブリュ． ファーガソン，ロバート; ティー． ブラディー，ジョン |
| 45 | JPS583905B2 - | JP14459777 | 1977-11-29 | JPS583905B2 | 1983-01-24 | JON SHII SHUUMAAKAA; ANDORE RAGENDEIKU |
| 46 | Method of and vessel for treating materials | JP14459777 | 1977-11-29 | JPS5369917A | 1978-06-21 | JIYON SHII SHIYUUMAAKAA; ANDORE RAGENDEIKU |
| 47 | SOLUTION PROCESS FOR INSB NANOPARTICLES AND APPLICATION FOR IR DETECTORS | US15578063 | 2016-05-06 | US20180163070A1 | 2018-06-14 | Ranjan Deepak DESHMUKH; Rebekah HOOKER; Yudhisthira SAHOO; Pawel MISKIEWICZ |
| This invention relates to a process for synthesizing InSb nanoparticles, a method to stabilize them, and a method to provide a photodetector to detect infrared light. | ||||||
| 48 | METHOD FOR REMOVING PENTAVALENT ANTIMONY CONTAMINANTS IN WATER AND FUEL CELL | US15622054 | 2017-06-13 | US20180115005A1 | 2018-04-26 | Guowang Zhou; Rujun TAO; Guanglv YU; Hao YU; Xiaodong LIN |
| The present invention provides a method for removing pentavalent antimony contaminants in water without adding a DC power supply and also provides a fuel cell capable of removing the pentavalent antimony contaminants in water by utilizing self-generated electric energy. A technical solution of the present invention is as follows: waste water is pumped into a reactor for reaction after a pH value of the waste water containing the pentavalent antimony contaminants adjusted to 3-6.5; the inside of a reactor is an anaerobic environment; and an iron anode is arranged in the reactor, a through hole is formed in a side wall of the reactor, a cathode for reducing oxygen by electrons and protons sealed and inlaid in the through hole, and a resistor is connected between the iron anode and the cathode in series. The present invention is suitable for a water treatment technology. | ||||||
| 49 | USE OF NOVEL COMPOUNDS AS NEGATIVE ELECTRODE ACTIVE MATERIAL IN A SODIUM-ION BATTERY | US14897255 | 2014-06-16 | US20160141611A1 | 2016-05-19 | Laure Monconduit; Ali Darwiche; Julien Fullenwarth; Lorenzo Stievano; Moulay Tahar Sougrati |
| Precursor compounds of sodium alloy(s), for use as negative electrode active material in a sodium-ion battery, as well as to a negative electrode have the precursor compound of sodium alloy(s), as well as a sodium-ion battery having a negative electrode of this kind. | ||||||
| 50 | Peroxide indicator | US14380853 | 2013-02-27 | US09244016B2 | 2016-01-26 | Ryo Karato; Nobuyuki Ando |
| An indicator for detecting peroxide can detect the peroxide through change of hue thereof by reacting the peroxide according to a predefined concentration and a predefined sterilization treatment condition thereof. The indicator has better resistance against weather or light and preservation stability than those of prior indicators including inorganic compounds or organic compounds as discoloration components, can clearly change an arbitrary hue thereof under suitable discoloration rate, and has visible distinguishability. The indicator for detecting peroxide includes powdery metal sulfide, that undergoes discoloration by reacting with the peroxide. In particular a discoloration layer including the metal sulfide is applied onto at least a portion of a base substrate. | ||||||
| 51 | ANTIMONY-DOPED TIN OXIDE POWDER AND METHOD OF PRODUCING THE SAME | US14388478 | 2013-03-28 | US20150090943A1 | 2015-04-02 | Shinya Shiraishi; Hirotoshi Umeda; Suzuo Sasaki |
| This antimony-doped tin oxide powder is an antimony-doped tin oxide powder characterized by: (A) including at least three kinds of ions selected from the group consisting of Sn2+, Sn4+, Sb3+ and Sb5+; (B) having a ratio of average Sn ionic radius to average Sb ionic radius of 1:(0.96 to 1.04); and (C) having an Sb content of 5 to 25 moles relative to a total of 100 moles of Sb and Sn, wherein the average Sn ionic radius is the average of ionic radii of Sn2+ and Sn4+, while the average Sb ionic radius is the average of ionic radii of Sb3+ and Sb5+. | ||||||
| 52 | P-TYPE OXIDE, COMPOSITION FOR PRODUCING P-TYPE OXIDE, METHOD FOR PRODUCING P-TYPE OXIDE, SEMICONDUCTOR ELEMENT, DISPLAY ELEMENT, IMAGE DISPLAY DEVICE, AND SYSTEM | US14360791 | 2012-11-28 | US20140353648A1 | 2014-12-04 | Yukiko Abe; Naoyuki Ueda; Yuki Nakamura; Mikiko Takada; Shinji Matsumoto; Yuji Sone; Ryoichi Saotome |
| To provide is a p-type oxide, including an oxide, wherein the oxide includes: Cu; and an element M, which is selected from p-block elements, and which can be in an equilibrium state, as being present as an ion, wherein the equilibrium state is a state in which there are both a state where all of electrons of p-orbital of an outermost shell are lost, and a state where all of electrons of an outermost shell are lost, and wherein the p-type oxide is amorphous. | ||||||
| 53 | Electrode active material for secondary battery and method for preparing the same | US13130153 | 2009-11-20 | US08546019B2 | 2013-10-01 | Yongju Lee; Jeyoung Kim; Oujung Kwon; Byung Hun Oh; Insung Uhm; Seungyoun Choi |
| The disclosure relates to an electrode active material including: (a) first particulate of a metal (or metalloid) oxide alloyable with lithium; and (b) second particulate of an oxide containing lithium and the same metal (or metalloid) as that of the metal (or metalloid) oxide, and to a secondary battery including the electrode active material. When the electrode active material is used as an anode active material, reduced amounts of an irreversible phase such as a lithium oxide or a lithium metal oxide are produced during initial charge-discharge of a battery since lithium is already contained in the second particulate before the initial charge-discharge, and thus a dead volume on the side of the cathode can be minimized and a high-capacity battery can be fabricated. | ||||||
| 54 | Method of producing stable oxygen terminated semiconducting nanoparticles | US12991879 | 2009-04-09 | US08434704B2 | 2013-05-07 | David Thomas Britton; Margit Harting |
| A method and apparatus of producing inorganic semiconducting nanoparticles having a stable surface includes providing an inorganic bulk semiconductor material milled in the presence of a selected reducing agent. The reducing agent acts to chemically reduce oxides of the semiconductor material, or prevent the formation of such oxides to provide semiconducting nanoparticles having a stable surface, allowing electrical contact between the nanoparticles. The milling media and/or one or more components of the mill include the selected reducing agent. The milling media or mill are typically composed of a metal selected from the group comprising iron, chromium, cobalt, nickel, tin, titanium, tungsten, vanadium, and aluminum, or an alloy containing one or more of these metals. Alternatively, the selected reducing agent includes a liquid contained in the mill during milling, which is typically an acidic solution containing any of hydrochloric, sulphuric, nitric, acetic, formic, or carbonic acid, or a mixture thereof. | ||||||
| 55 | ELECTRODE ACTIVE MATERIAL FOR SECONDARY BATTERY AND METHOD FOR PREPARING THE SAME | US13130153 | 2009-11-20 | US20110311875A1 | 2011-12-22 | Yongju Lee; Jeyoung Kim; Oujung Kwon; Byung Hun Oh; Insung Uhm; Seungyoun Choi |
| The disclosure relates to an electrode active material including: (a) first particulate of a metal (or metalloid) oxide alloyable with lithium; and (b) second particulate of an oxide containing lithium and the same metal (or metalloid) as that of the metal (or metalloid) oxide, and to a secondary battery including the electrode active material. When the electrode active material is used as an anode active material, reduced amounts of an irreversible phase such as a lithium oxide or a lithium metal oxide are produced during initial charge-discharge of a battery since lithium is already contained in the second particulate before the initial charge-discharge, and thus a dead volume on the side of the cathode can be minimized and a high-capacity battery can be fabricated. | ||||||
| 56 | Composite compound with mixed crystalline structure | US12316173 | 2008-12-09 | US08052897B2 | 2011-11-08 | Xiaobing Xi; Tangli Cheng; Ye Tian; Lu Bai; Xiaoli Yin |
| A composite lithium compound having a mixed crystalline structure is provided. Such compound can be formed by heating lithium, iron, phosphorous and carbon sources with a lithium metal compound. The resulting mixed metal crystal can exhibit superior electrical property and is a better cathode material for lithium secondary batteries. | ||||||
| 57 | Composite compound with mixed crystalline structure | US12316173 | 2008-12-09 | US20090220860A1 | 2009-09-03 | Xiaobing Xi; Tangli Cheng; Ye Tian; Lu Bai; Xiaoli Yin |
| A composite lithium compound having a mixed crystalline structure is provided. Such compound can be formed by heating lithium, iron, phosphorous and carbon sources with a lithium metal compound. The resulting mixed metal crystal can exhibit superior electrical property and is a better cathode material for lithium secondary batteries. | ||||||
| 58 | Method for obtaining the nano-scale acicular oxidation compound powder | US11706233 | 2007-02-15 | US20080199394A1 | 2008-08-21 | Hsin-Chun Lu; Mei-Ching Chiang; Kai-Yi Wang; Yu-Hsiang Lin |
| The invention, firstly, SnCl4 and SbCl3 are collected as raw materials and all dissolved into water and hydrochloric acid with precipitation. Secondly, NaOH or NH40H can be used for adjusting the pH value. Then, aging, water-washing, filtering and drying process are all carried out. The additive also can be put into and sintering process is applied. Furthermore, washing and drying process are used for obtaining the crystalline nano-level acicular ATO composition powder. | ||||||
| 59 | Nanoparticles having a rutile-like crystalline phase and method of preparing same | US09990604 | 2001-11-21 | US06962946B2 | 2005-11-08 | John T. Brady; David S. Arney; Robert W. Ferguson; James A. Higgins; Charles J. Studiner, IV |
| Nanometer-sized particles comprise a mixed oxide of titanium and antimony and are characterized by rutile-like crystal phases. The particles are easily prepared by hydrothemal processing, and may be used as colloids, or in various compositions and articles. | ||||||
| 60 | Low visibility laser marking additive | US10976777 | 2004-11-01 | US20050137305A1 | 2005-06-23 | James Carroll; Steven Jones |
| Laser marking of plastic material is achieved by incorporating into the plastic a laser marking particulate additive having a particle size of less than 100 nm. A mixed oxide particle of tin and antimony having a particle size of 10-70 nm is useful as a laser marking additive when using a YAG laser. A metallic powder can further be added to improve marking contrast. | ||||||
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