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Impact of Synthesis Methods on the Transport of Single Walled Carbon Nanotubes in the Aquatic Environment

机译:合成方法对单壁碳纳米管在水环境中迁移的影响

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摘要

In this study, a systematic approach has been followed to investigate the fate and transport of single walled carbon nanotubes (SWCNTs) from synthesis to environmentally relevant conditions. Three widely used SWCNT synthesis methods have been investigated in this study including high pressure carbon monoxide (HiPco), SWeNT CoMoCat, and electric arc discharge technique (EA). This study relates the transport of three SWCNTs (HiPco-D, SG65-D, and P2-D) with different synthesis methods and residual catalyst content revealing their influence on the subsequent fate of the nanotubes. To minimize nanotube bundling and aggregation, the SWCNTs were dispersed using the biocompatible triblock copolymer Pluronic, which allowed the comparison in the transport trends among these SWCNTs. After purification, the residual metal catalyst between the SWCNTs follows the trend: HiPco-D > SG65-D > P2- D. The electrophoretic mobility (EPM) and hydrodynamic diameter of SWCNTs remained insensitive to SWCNT type, pH, and presence of natural organic matter (NOM); but were affected by ionic strength (IS) and ion valence (K~+, Ca~(2+)). In monovalent ions, the hydrodynamic diameter of SWCNTs was not influenced by IS, whereas larger aggregation was observed for HiPco-D with IS than P2-D and SG65-D in the presence of Ca~(2+). Transport of HiPco-D in the porous media was significantly higher than SG65-D followed by P2-D. Release of HiPco-D from porous media was higher than SG6S-D followed by P2-D, though negligible amount of all types of SWCNTs (<5%) was released. Both transport and release patterns follow a similar trend to what was observed for residual metal catalysts in SWCNTs. Addition of NOM increased the transport of all SWCNTs primarily due to electrosteric repulsion. HiPco-D was notably more acidic than SG65-D followed by P2-D, which is similar to the transport trend. Overall, it was observed that the synthesis methods resulted in distinctive breakthrough trends, which were correlated to metal content These findings will facilitate the safe design of environmental friendly SWCNTs by minimizing mobility in aquatic environments.
机译:在这项研究中,已遵循一种系统的方法来研究单壁碳纳米管(SWCNT)从合成到环境相关条件的命运和运输。在这项研究中,研究了三种广泛使用的SWCNT合成方法,包括高压一氧化碳(HiPco),SWeNT CoMoCat和电弧放电技术(EA)。这项研究将三种SWCNT(HiPco-D,SG65-D和P2-D)的运输方法与不同的合成方法和残留的催化剂含量联系起来,揭示了它们对纳米管后续命运的影响。为了最小化纳米管的束缚和聚集,使用生物相容性三嵌段共聚物Pluronic分散了SWCNT,从而可以比较这些SWCNT之间的传输趋势。纯化后,SWCNT之间的残留金属催化剂遵循以下趋势:HiPco-D> SG65-D> P2-D。SWCNT的电泳迁移率(EPM)和流体力学直径对SWCNT类型,pH和天然有机物的存在不敏感物质(NOM);但受离子强度(IS)和离子价(K〜+,Ca〜(2+))的影响。在单价离子中,SWCNTs的流体动力学直径不受IS的影响,而在有Ca〜(2+)的情况下,带有IS的HiPco-D的聚集作用大于P2-D和SG65-D。 HiPco-D在多孔介质中的转运明显高于SG65-D,其次是P2-D。 HiPco-D从多孔介质中的释放高于SG6S-D,其次是P2-D,尽管所有类型的SWCNT的释放量都可以忽略不计(<5%)。转运和释放方式都遵循与SWCNT中残留金属催化剂相似的趋势。 NOM的添加主要是由于空间电斥力增加了所有SWCNT的传输。 HiPco-D的酸性明显高于SG65-D,其次是P2-D,这与运输趋势相似。总的来说,观察到合成方法导致了独特的突破趋势,这与金属含量有关。这些发现将通过最大程度地减少在水生环境中的迁移率而促进安全环保的碳纳米管的设计。

著录项

  • 来源
    《Environmental Science & Technology》 |2012年第21期|11752-11760|共9页
  • 作者单位

    Department of Chemical and Environmental Engineering, University of California, Riverside, California 92521, United States;

    Departments of Material Science and Engineering, Chemistry, and Medicine, Northwestern University, Evanston, Illinois 60201, United States;

    Departments of Material Science and Engineering, Chemistry, and Medicine, Northwestern University, Evanston, Illinois 60201, United States;

    Departments of Material Science and Engineering, Chemistry, and Medicine, Northwestern University, Evanston, Illinois 60201, United States;

    Department of Chemical and Environmental Engineering, University of California, Riverside, California 92521, United States;

  • 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);
  • 原文格式 PDF
  • 正文语种 eng
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