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Evidence of Water Adsorption in Hydrophobic Nanospaces of Highly Pure Double-Walled Carbon Nanotubes

机译:高纯双壁碳纳米管疏水纳米空间中水吸附的证据

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The adsorption of water vapor by carbon nanotubes and othernnarrow channels is receiving increasing attention in physical,nchemical, and biological sciences owing to its promise for practicalnapplications such as separation and purification, selective chemicalnsensing, and the efficient design and operation of micro- andnnanofluidic devices. As explained by Sansom and Biggin, one wouldnnot intuitively expect water to enter a narrow hydrophobic carbonnnanotube, but computer simulations surprise us to show that it can.1nThis adsorption phenomenon can also provide clues about thenbehavior of biological pores.1,2 Single-walled carbon nanotubesn(SWCNTs) as well as multiwalled carbon nanotubes (MWCNTs)nwith rigid, chemically simple, and well-defined nanopores providena model system for investigation into the behavior of nanoconfinedninterfacial water, and thus water adsorption by SWCNTs andnMWCNTs has been extensively investigated by means of molecularndynamics (MD) simulations.2,3 Recently, nuclear magnetic resonancenmeasurements have been used to construct water adsorptionnisotherms in SWCNTs.4 Hummer et al. have found that, withinnsubnanometer-diameter channels of SWCNTs, water undergoes anone-dimensional ordering, which leads to a concerted, pulse-likenmovement of water molecules within the nanotube channels duento the tightness of the hydrogen bonding network among the waternmolecules.3 Wang et al. have reported that the hydrophobicity ofnnanoconfined SWCNT surfaces should not be considered annabsolute property without considering the structure of interfacialnwater.4 Their study corroborates the proposal that carbon nanoconfinementnfavors the formation of clusters of water moleculesnand that as these clusters grow the SWCNT pores becomeneffectively hydrophilic.5 These intriguing progresses have givennrise to an intensive interest in water adsorption in nanoscale poresnof carbon nanotubes (CNTs). We need to obtain new knowledgenof water adsorption on different types of CNTs.5,6
机译:碳纳米管和其他窄通道对水蒸气的吸附在物理,化学和生物科学领域受到越来越多的关注,这是由于其有望用于实际应用,例如分离和纯化,选择性化学传感以及微纳米流体装置的高效设计和操作。正如Sansom和Biggin所解释的那样,人们不会凭直觉期望水会进入狭窄的疏水性碳纳米管,但是计算机模拟使我们惊讶地发现水可以做到这一点。1n这种吸附现象还可以提供有关生物孔隙行为的线索。1,2单壁碳具有刚性,化学简单且定义明确的纳米孔的碳纳米管n(SWCNTs)和多壁碳纳米管(MWCNTs)为研究纳米共界面界面水的行为提供了一个模型系统,因此,SWCNTs和nMWCNTs对水的吸附已被广泛研究。分子动力学模拟[2,3]。最近,核磁共振测量已被用于构建SWCNT中的水吸附等温线。4Hummer等人。已经发现,在短壁碳纳米管的亚纳米直径通道内,水经历一维有序的运动,由于水分子之间氢键网络的紧密性,水导致纳米管通道内水分子的一致脉冲状运动。3Wang等。已有报道称,在不考虑界面水结构的情况下,不应将纳米约束的SWCNT表面的疏水性视为绝对性质。4他们的研究证实了碳纳米约束有利于水分子簇的形成的建议,并且随着这些簇的生长,SWCNT的孔将变得无效。5有趣的进展引起人们对碳纳米管(CNT)纳米孔中水吸附的浓厚兴趣。我们需要获得有关不同类型的CNT的水吸附的新知识。5,6

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  • 来源
    《Journal of the American Chemical Society》 |2010年第4期|p.1214-1215|共2页
  • 作者单位

    Institute of Carbon Science and Technology, Shinshu UniVersity, Nagano 380-8553, Japan, and Graduate School ofScience, Chiba UniVersity, Chiba 263-8522, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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