4.6 Article

Combined determination analysis of surface properties evolution towards bentonite by pH treatments

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DOI: 10.1016/j.colsurfa.2021.127067

关键词

Charged clay surface; Surface charge properties; Ion exchange; Protonation; Dissolution

资金

  1. Doctoral Start-Up Research Fund of Northwest AF University [2452018041]
  2. Open Fund of State Key Laboratory of Soil Erosion and Dryland Farming on the Loess Plateau [A314021402-1906]
  3. National Key Research and Development Program of China [2017YFD0200205]

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This study investigated the evolution of surface properties of bentonite clay under different pH conditions, revealing that the surface potential, surface electric field strength, and surface charge numbers of bentonite are influenced by pH variations. The results showed that the surface potential of bentonite is considerably negative and more sensitive to pH changes, while the surface electric field strength and surface charge numbers are inversely proportional to hydrogen ion concentrations at multiple pH settings.
Bentonite possesses multiple physicochemical properties because of a large number of charges on the surface. Understanding charges-related surface characteristics at various aqueous solution conditions is critical for bentonite application in various fields, including material modification and environmental restoration. In this study, the evolution of surface properties (surface potential, surface electric field strength, specific surface area, and surface charge numbers) for bentonite samples was investigated using simple ion-exchange experiments and extended combined determination method at different pH conditions. Zeta potential, X-ray diffraction (XRD), and attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR) techniques were used to examine changes in bentonite structure and surface functional groups. The results demonstrated that surface potential was considerably negative (larger in absolute value) and more sensitive to pH variation than the zeta potential of bentonite under identical conditions. At multiple pH settings, the surface electric field strength and the numbers of bentonite's surface charges were inversely proportional to hydrogen ion concentrations. Cations covalently bonded to clay's surface might reduce negative surface charges and diminish surface electric field strength, particularly as ionic strength increased. Although moderate pH variation has no discernible effect on bentonite interlayer structural alterations, moderate clay dissolution and changes in mineralogical properties may increase the specific surface area of bentonite, particularly when the solvent chemical conditions are acidic. This study comprehensively sheds light on the evolution of surface properties of bentonite clay under acidic, neutral and alkaline conditions, which is helpful in understanding and optimizing its surface performance for material and environmental applications.

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