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    • 52. 发明授权
    • Epitaxial growth and cloning of a precursor chiral nanotube
    • 外延生长和克隆前体手性纳米管
    • US08038795B2
    • 2011-10-18
    • US12174356
    • 2008-07-16
    • Delmar L. BarkerWilliam R. Owens
    • Delmar L. BarkerWilliam R. Owens
    • C30B25/18
    • C30B29/602B82Y30/00B82Y40/00C01B32/16C01B33/02C01B35/023C30B11/12C30B25/00C30B29/02Y10S977/722Y10S977/734Y10S977/74Y10S977/742Y10S977/748Y10S977/75Y10S977/751
    • A precursor chiral nanotube with a specified chirality is grown using an epitaxial process and then cloned. A substrate is provided of crystal material having sheet lattice properties complementary to the lattice properties of the selected material for the nanotube. A cylindrical surface(s) having a diameter of 1 to 100 nanometers are formed as a void in the substrate or as crystal material projecting from the substrate with an orientation with respect to the axes of the crystal substrate corresponding to the selected chirality. A monocrystalline film of the selected material is epitaxially grown on the cylindrical surface that takes on the sheet lattice properties and orientation of the crystal substrate to form a precursor chiral nanotube. A catalytic particle is placed on the precursor chiral nanotube and atoms of the selected material are dissolved into the catalytic particle to clone a chiral nanotube from the precursor chiral nanotube.
    • 使用外延工艺生长具有指定手性的前体手性纳米管,然后克隆。 提供了具有与所选择的纳米管材料的晶格特性互补的片状晶格特性的晶体材料的衬底。 形成直径为1至100纳米的圆柱形表面作为基底中的空隙,或者形成为相对于与所选择的手性对应的晶体基板的轴线从基板突出的晶体材料。 所选材料的单晶膜在圆柱形表面上外延生长,该圆柱形表面承受晶体基板的晶格特性和取向以形成前体手性纳米管。 将催化颗粒置于前体手性纳米管上,并将所选材料的原子溶解到催化颗粒中以从前体手性纳米管克隆手性纳米管。
    • 54. 发明授权
    • Carbon nanotube structure-selective separation and surface fixation
    • 碳纳米管结构选择性分离和表面固定
    • US07785472B2
    • 2010-08-31
    • US10597790
    • 2005-02-10
    • Kei Murakoshi
    • Kei Murakoshi
    • B01D15/08C09C1/44
    • H01M4/96B82Y15/00B82Y30/00B82Y40/00C01B32/172C01B2202/02C01B2202/30C01B2202/36G01N2030/8859G01P15/08G01P15/0802H01M4/8605H01M4/9083Y10S977/745Y10S977/748Y10S977/751Y10S977/845Y10S977/848
    • A method of separating, concentrating or purifying uniform carbon nanotubes with desired properties (diameter, chiral vector, etc) in a highly sensitive manner by the use of structure-sensitive properties peculiar to carbon nanotubes; and an apparatus therefor. There is provided a method of separating, concentrating, or purifying carbon nanotubes with the desired properties contained in a sample, comprising the steps of (a) irradiating a sample containing carbon nanotubes with light; and (b) selecting carbon nanotubes with desired properties. In a preferred embodiment, the light irradiation of the step (a) can be carried out in the presence of a metal so as to cause specified carbon nanotubes to selectively induce a photocatalytic reaction, resulting in metal deposition. Further, in a preferred embodiment, a given magnetic filed can be applied in the steps (b) so as to attain accumulation or concentration or carbon nanotubes with metal deposited.
    • 通过使用碳纳米管特有的结构敏感性质,以高度敏感的方式分离,浓缩或纯化具有所需性质(直径,手性载体等)的均匀碳纳米管的方法; 及其装置。 提供了一种分离,浓缩或净化样品中包含的所需性质的碳纳米管的方法,包括以下步骤:(a)用光照射含有碳纳米管的样品; 和(b)选择具有所需性质的碳纳米管。 在优选的实施方案中,步骤(a)的光照射可以在金属的存在下进行,以使特定的碳纳米管选择性地诱导光催化反应,导致金属沉积。 此外,在优选实施例中,可以在步骤(b)中施加给定的磁场,以便获得积聚或浓缩或者沉积金属的碳纳米管。
    • 58. 发明授权
    • Single-wall carbon nanotubes from high pressure CO
    • 单壁碳纳米管由高压CO
    • US07204970B2
    • 2007-04-17
    • US10730630
    • 2003-12-08
    • Richard E. SmalleyKen A. SmithDaniel T. ColbertPavel NikolaevMichael J. BronikowskiRobert K. BradleyFrank Rohmund
    • Richard E. SmalleyKen A. SmithDaniel T. ColbertPavel NikolaevMichael J. BronikowskiRobert K. BradleyFrank Rohmund
    • C01B11/02
    • B01J4/002B01J3/04B01J3/042B01J19/121B01J19/26B01J2219/0875B82Y30/00B82Y40/00C01B32/162C01B2202/02C01B2202/36D01F9/1278Y10S977/75Y10S977/751Y10S977/843Y10S977/845Y10S977/951Y10T428/30
    • The present invention discloses the process of supplying high pressure (e.g., 30 atmospheres) CO that has been preheated (e.g., to about 1000° C.) and a catalyst precursor gas (e.g., Fe(CO)5) in CO that is kept below the catalyst precursor decomposition temperature to a mixing zone. In this mixing zone, the catalyst precursor is rapidly heated to a temperature that results in (1) precursor decomposition, (2) formation of active catalyst metal atom clusters of the appropriate size, and (3) favorable growth of SWNTs on the catalyst clusters. Preferably a catalyst cluster nucleation agency is employed to enable rapid reaction of the catalyst precursor gas to form many small, active catalyst particles instead of a few large, inactive ones. Such nucleation agencies can include auxiliary metal precursors that cluster more rapidly than the primary catalyst, or through provision of additional energy inputs (e.g., from a pulsed or CW laser) directed precisely at the region where cluster formation is desired. Under these conditions SWNTs nucleate and grow according to the Boudouard reaction. The SWNTs thus formed may be recovered directly or passed through a growth and annealing zone maintained at an elevated temperature (e.g., 1000° C.) in which tubes may continue to grow and coalesce into ropes.
    • 本发明公开了提供已被预热(例如,约1000℃)的高压(例如30个大气压)的CO和催化剂前体气体(例如Fe(CO)5) >)在CO中,其保持低于催化剂前体分解温度至混合区。 在该混合区中,将催化剂前体快速加热到导致(1)前体分解的温度,(2)形成适当尺寸的活性催化剂金属原子簇,和(3)在催化剂簇上的SWNT的有利生长 。 优选使用催化剂簇成核剂来使催化剂前体气体快速反应以形成许多小的活性催化剂颗粒,而不是几个大的非活性催化剂颗粒。 这样的成核机构可以包括比主要催化剂更快地聚集的辅助金属前体,或者通过提供精确地指向需要簇形成的区域的额外的能量输入(例如来自脉冲或CW激光)。 在这些条件下,SWNT根据Boudouard反应成核并生长。 如此形成的SWNT可以直接回收或通过保持在高温(例如1000℃)的生长和退火区域,其中管可以继续生长并聚结成绳索。
    • 60. 发明申请
    • Single-wall carbon nanotubes from high pressure CO
    • 单壁碳纳米管由高压CO
    • US20040223901A1
    • 2004-11-11
    • US10730630
    • 2003-12-08
    • William Marsh Rice University
    • Richard E. SmalleyKen A. SmithDaniel T. ColbertPavel NikolaevMichael J. BronikowskiRobert K. BradleyFrank Rohmund
    • D01F009/12
    • B01J4/002B01J3/04B01J3/042B01J19/121B01J19/26B01J2219/0875B82Y30/00B82Y40/00C01B32/162C01B2202/02C01B2202/36D01F9/1278Y10S977/75Y10S977/751Y10S977/843Y10S977/845Y10S977/951Y10T428/30
    • The present invention discloses the process of supplying high pressure (e.g., 30 atmospheres) CO that has been preheated (e.g., to about 1000null C.) and a catalyst precursor gas (e.g., Fe(CO)5) in CO that is kept below the catalyst precursor decomposition temperature to a mixing zone. In this mixing zone, the catalyst precursor is rapidly heated to a temperature that results in (1) precursor decomposition, (2) formation of active catalyst metal atom clusters of the appropriate size, and (3) favorable growth of SWNTs on the catalyst clusters. Preferably a catalyst cluster nucleation agency is employed to enable rapid reaction of the catalyst precursor gas to form many small, active catalyst particles instead of a few large, inactive ones. Such nucleation agencies can include auxiliary metal precursors that cluster more rapidly than the primary catalyst, or through provision of additional energy inputs (e.g., from a pulsed or CW laser) directed precisely at the region where cluster formation is desired. Under these conditions SWNTs nucleate and grow according to the Boudouard reaction. The SWNTs thus formed may be recovered directly or passed through a growth and annealing zone maintained at an elevated temperature (e.g., 1000null C.) in which tubes may continue to grow and coalesce into ropes.
    • 本发明公开了在被保留的CO中提供已被预热(例如,约1000℃)的高压(例如,30个大气压)的CO和催化剂前体气体(例如,Fe(CO)5)的过程。 催化剂前体分解温度低于混合区。 在该混合区中,将催化剂前体快速加热到导致(1)前体分解的温度,(2)形成适当尺寸的活性催化剂金属原子簇,和(3)在催化剂簇上的SWNT的有利生长 。 优选使用催化剂簇成核剂来使催化剂前体气体快速反应以形成许多小的活性催化剂颗粒,而不是几个大的非活性催化剂颗粒。 这样的成核机构可以包括比主要催化剂更快地聚集的辅助金属前体,或者通过提供精确地指向需要簇形成的区域的额外的能量输入(例如来自脉冲或CW激光)。 在这些条件下,SWNT根据Boudouard反应成核并生长。 如此形成的SWNT可以直接回收或通过保持在高温(例如1000℃)的生长和退火区域,其中管可以继续生长并聚结成绳索。