• DocumentCode
    3151429
  • Title

    Research on adsorption mechanism and regeneration of organic modified montmorillonite

  • Author

    Miao, Xianfeng ; Gu, Linyuan ; Na, Ping

  • Author_Institution
    Sch. of Chem. Eng. & Technol., Tianjin Univ., Tianjin, China
  • fYear
    2011
  • fDate
    16-18 April 2011
  • Firstpage
    5163
  • Lastpage
    5166
  • Abstract
    The adsorption of thiophene from thiophene-octane mixture has been investigated using organic-montmorillonite under proper conditions. The adsorbents were prepared by a xerogel process, followed by thermo - treatment. The adsorptive experiments show that C-P-MMT adsorbent has the higher capacity, 3.8mg/g (mg of sulfur per g of adsorbent). BET, XRD, NMR were used to characterize the adsorbents. It was found that a new spinel-phase was formed during thermal treatment, and the layer spacing of C-P-MMT absorbent was larger than that of Na-MMT. The organic montmorillonite prepared by PTMAB and CTMAB has lower crystallinity and surface area but larger pore diameter than it was prepared only by PTMAB. The XRD and NMR results also showed that the structure of the adsorbents has not changed after adsorption, suggesting that the prepared adsorbents could be easily regenerated.
  • Keywords
    X-ray diffraction; adsorption; aerogels; clay; heat treatment; nuclear magnetic resonance; organic compounds; BET; NMR; XRD; adsorbents; adsorption; cetyltrimethylammonium bromide; crystallinity; organic modified montmorillonite; phenyl-trimethyl ammonium bromide; regeneration; spinel-phase; surface area; thermal treatment; thiophene-octane mixture; xerogel process; Compounds; Nuclear magnetic resonance; Petroleum; Surface treatment; X-ray diffraction; X-ray scattering; adsorption mechanism; deep desulfurization; modified MMT;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Consumer Electronics, Communications and Networks (CECNet), 2011 International Conference on
  • Conference_Location
    XianNing
  • Print_ISBN
    978-1-61284-458-9
  • Type

    conf

  • DOI
    10.1109/CECNET.2011.5768392
  • Filename
    5768392