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    • 4. 发明申请
    • POLYMERIZATION INITIATED AT THE SIDEWALLS OF CARBON NANOTUBES
    • 碳纳米管的开发聚合
    • WO2005030858A3
    • 2005-06-23
    • PCT/US2004019769
    • 2004-06-21
    • UNIV RICE WILLIAM MUNIV HOUSTONTOUR JAMES MHUDSON JARED LKRISHNAMOORTI RAMANANYURELKI KORAYMITCHELL CYNTHIA A
    • TOUR JAMES MHUDSON JARED LKRISHNAMOORTI RAMANANYURELKI KORAYMITCHELL CYNTHIA A
    • C01B31/02C08F292/00C08K3/04C08K7/06C08K7/24
    • C08F4/484B82Y30/00B82Y40/00C01B32/174C01B2202/02C08F2/00C08F112/08C08F292/00C08K3/041C08K9/04C08L67/04
    • The present invention is directed to aryl halide (such as aryl bromide) functionalized carbon nanotubes can be utilized in anionic polymerization processes to form polymer-carbon nanotube materials with improved dispersion ability in polymer matrices. In this process the aryl halide is reacted with an alkyllithium species or is reacted with a metal to replace the aryl-bromine bond with an aryl-lithium or aryl-metal bond, respectively. It has further been discovered that other functionalized carbon nanotubes, after deprotonation with a deprotonation agent, can similarly be utilized in anionic polymerization processes to form polymer-carbon nanotube materials. Additionally or alternatively, a ring opening polymerization process can be performed. The resultant materials can be used by themselves due to their enhanced strength and reinforcement ability when compared to their unbound polymer analogs. Additionally, these materials can also be blended with pre-formed polymers to establish compatibility and enhanced dispersion of nanotubes in otherwise hard to disperse matrices resulting in significantly improved material properties. The resultant polymer-carbon nanotube materials can also be used in drug delivery processes due to their improved dispersion ability and biodegradability, and can also be used for scaffolding to promote cellular growth of tissue.
    • 本发明涉及芳基卤化物(例如芳基溴化物)官能化碳纳米管可以用于阴离子聚合方法以形成具有改进的聚合物基质分散能力的聚合物 - 碳纳米管材料。 在该方法中,芳基卤化物与烷基锂物质反应,或与金属反应,分别用芳基 - 锂或芳基 - 金属键代替芳基 - 溴键。 还已经发现,其它官能化碳纳米管在去质子化脱质子化之后,可以类似地用于阴离子聚合方法中以形成聚合物 - 碳纳米管材料。 另外或者可选地,可以进行开环聚合方法。 所得材料由于与未结合的聚合物类似物相比具有增强的强度和增强能力,可以自己使用。 另外,这些材料也可以与预先形成的聚合物混合以建立纳米管在其它难分散的基质中的相容性和增强的分散,导致显着改善的材料性质。 所得聚合物 - 碳纳米管材料由于其分散能力和生物降解性的改善而可用于药物递送过程中,并且也可用于支架以促进组织的细胞生长。
    • 8. 发明申请
    • HIGHLY OXIDIZED GRAPHENE OXIDE AND METHODS FOR PRODUCTION THEREOF
    • 高度氧化的氧化石墨及其生产方法
    • WO2011016889A3
    • 2011-04-21
    • PCT/US2010034905
    • 2010-05-14
    • UNIV RICE WILLIAM MTOUR JAMES MKOSYNKIN DMITRY V
    • TOUR JAMES MKOSYNKIN DMITRY V
    • C01B31/00
    • C01B31/0476B82Y30/00B82Y40/00C01B32/192C01B32/23C09K8/032
    • A highly oxidized form of graphene oxide and methods for production thereof are described in various embodiments of the present disclosure. In general, the methods include mixing a graphite source with a solution containing at least one oxidant and at least one protecting agent and then oxidizing the graphite source with the at least one oxidant in the presence of the at least one protecting agent to form the graphene oxide. Graphene oxide synthesized by the presently described methods is of a high structural quality that is more oxidized and maintains a higher proportion of aromatic rings and aromatic domains than does graphene oxide prepared in the absence of at least one protecting agent. Methods for reduction of graphene oxide into chemically converted graphene are also disclosed herein. The chemically converted graphene of the present disclosure is significantly more electrically conductive than is chemically converted graphene prepared from other sources of graphene oxide.
    • 在本公开的各种实施例中描述了氧化石墨烯的高度氧化形式及其生产方法。 通常,所述方法包括将石墨源与含有至少一种氧化剂和至少一种保护剂的溶液混合,然后在至少一种保护剂存在下用至少一种氧化剂氧化石墨源以形成石墨烯 氧化物。 通过目前描述的方法合成的氧化石墨烯具有较高的结构质量,其比没有至少一种保护剂时制备的石墨烯氧化物更多地被氧化并保持较高比例的芳族环和芳族域。 本文还公开了将氧化石墨烯还原成化学转化的石墨烯的方法。 本公开内容的化学转化的石墨烯与由其他石墨烯氧化物源制备的化学转化的石墨烯相比导电性明显更高。