4.8 Article

Unique Lead Adsorption Behavior of Activated Hydroxyl Group in Two-Dimensional Titanium Carbide

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 136, Issue 11, Pages 4113-4116

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja500506k

Keywords

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Funding

  1. NSFC [51101142, 50821001, 51102206, 21207112]
  2. NSF of Hebei [B2012203060, 13961002D]
  3. Program for New Century Excellent Talents in University of Ministry of Education of China [NCET-12-0690]
  4. China Postdoctoral Science Foundation [2013T60265]
  5. Foundation for the Excellent Youth Scholars from Universities and Colleges of Hebei Province [Y2011113, Y2012019]

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The functional groups and site interactions on the surfaces of two-dimensional (20) layered titanium carbide can be tailored to attain some extraordinary physical properties. Herein a 20 alk-MXene (Ti3C2(OH/ONa)(x)F-2_x) material, prepared by chemical exfoliation followed by alkalization intercalation, exhibits preferential Pb(II) sorption behavior when competing cations (Ca-(II)/Mg(II)) coexisted at high levels. Kinetic tests show that the sorption equilibrium is achieved in as short a time as 120 s. Attractively, the alk-MXene presents efficient Pb(II) uptake performance with the applied sorption capacities of 4500 kg water per alk-MXene, and the effluent Pb(II) contents are below the drinking water standard recommended by the World Health Organization (10 mu g/L). Experimental and computational studies suggest that the sorption behavior is related to the hydroxyl groups in activated Ti sites, where Pb(II) ion exchange is facilitated by the formation of a hexagonal potential trap.

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