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Graphene oxide-assisted preparation of poly(vinyl alcohol)/carbon nanotube/reduced graphene oxide nanofibers with high carbon content by electrospinning technology

机译:通过静电纺丝技术通过高碳含量的聚(乙烯醇)/碳纳米管/碳纳米管/碳纳米管/碳纳米氧化物纳米纤维的辅助制备

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摘要

In this article, poly(vinyl alcohol) (PVA) based nanofibers with high carbon content were prepared via electrospinning technology. Graphene oxide (GO) was used as the dispersing agent to improve the dispersion of the multi-walled carbon nanotubes (MWCNTs) in the electrospinning solution and the PVA based nanofibers, and as the precursor of graphene. The microstructure of the PVA/GO/MWCNT nanofibers was examined via field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM). The FESEM/TEM results show that the MWCNTs were dispersed well in the PVA matrix with the assistance of GO. The stability of the PVA/GO/MWCNT nanofiber mat in aqueous solution is enhanced via the crosslinked network formed after crosslinking with glutaraldehyde (GA). Then, a PVA/RGO/MWCNT nanofiber mat was obtained by the reduction of GO after the crosslinked PVA/GO/MWCNT nanofiber mat was soaked in hydrazine hydrate solution. The ID/IG value of the GO in the nanofibers increased from 0.83 to 1.11 after reduction with hydrazine hydrate at 95 ° C for 1 hour, which indicated that the reduction of GO did take place. After the addition of GO, the tensile strength of the PVA nanofiber mat decreased from 16.7 ± 0.7 MPa to 13.2 ± 0.8 MPa. After the addition of MWCNTs, the tensile strength of the PVA/GO nanofiber mat increased from 13.2 ± 0.8 MPa to 18.1 ± 0.5 MPa. At the same time, the crosslinked network also enhanced the tensile strength of these nanofiber mats. The volume conductivity of the PVA nanofiber mat increased from 5.11 ± 0.96 × 10~(-11) Sm~(-1) to 2.33 ± 0.20 × 10~(-7) Sm~(-1) when the carbon content in the PVA based nanofibers reached 21 wt%.
机译:在本文中,通过静电纺丝技术制备具有高碳含量高碳含量的聚(乙烯醇)(PVA)的纳米纤维。将石墨烯氧化物(GO)用作分散剂,以改善多壁碳纳米管(MWCNT)在静电纺丝溶液和PVA基纳米纤维中的分散,以及作为石墨烯的前​​体。通过现场发射扫描电子显微镜(FESEM)和透射电子显微镜(TEM)检查PVA / GO / MWCNT纳米纤维的微观结构。 FeSEM / TEM结果表明,在PVA矩阵中,MWCNTS在GO的帮助下分散很好。通过与戊二醛(GA)交联后形成的交联网络,通过交联网络增强了PVA / GO / MWCNT纳米纤维垫的稳定性。然后,通过在肼水合物溶液中浸泡交联的PVA / GO / MWCNT纳米纤维垫之后,通过减少PVA / RGO / MWCNT纳米纤维垫。在用95℃下用肼水合物减少1小时后,纳米纤维的纳米纤维的ID / Ig值从0.83升至1.11增加,这表明持续的DE减少。添加后,PVA纳米纤维垫的拉伸强度从16.7±0.7MPa降低至13.2±0.8MPa。添加MWCNT后,PVA / Go纳米纤维垫的拉伸强度从13.2±0.8MPa增加到18.1±0.5MPa。同时,交联网络也增强了这些纳米纤维垫的拉伸强度。该PVA纳米纤维垫的体积电导率从5.11增加到±0.96×10〜(-11)的Sm〜(-1)至2.33±0.20×10〜(-7)的Sm〜(-1)时在PVA中的碳含量基于纳米纤维达到21重量%。

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  • 来源
    《RSC Advances》 |2015年第111期|共10页
  • 作者单位

    College of Materials Science and Engineering Nanjing Tech University Nanjing 210009 China.;

    College of Materials Science and Engineering Nanjing Tech University Nanjing 210009 China.;

    College of Materials Science and Engineering Nanjing Tech University Nanjing 210009 China.;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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