A study of factors affecting on the zeta potential of kaolinite and quartz powder

Yukselen-Aksoy Y., Kaya A.

ENVIRONMENTAL EARTH SCIENCES, cilt.62, sa.4, ss.697-705, 2011 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 62 Sayı: 4
  • Basım Tarihi: 2011
  • Doi Numarası: 10.1007/s12665-010-0556-9
  • Dergi Adı: ENVIRONMENTAL EARTH SCIENCES
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.697-705
  • Anahtar Kelimeler: Isoelectric point, Kaolinite, pH, Quartz, Zeta potential, HYDROLYZABLE METAL-IONS, ELECTROKINETIC PROPERTIES, INTERFACIAL BEHAVIOR, SOIL REMEDIATION, ADSORPTION, MICROELECTROPHORESIS, SUSPENSIONS, MINERALS, CHARGE
  • Dokuz Eylül Üniversitesi Adresli: Hayır

Özet

The purpose of this study was to determine the effects of pH, ion type (salt and metal cations), ionic strength, cation valence, hydrated ionic radius, and solid concentration on the zeta potential of kaolinite and quartz powder in the presence of NaCl, KCl, CaCl2, CuCl2, BaCl2, and AlCl3 solutions. The kaolinite and quartz powder have no isoelectric point (iep) within the entire pH range (3 < pH < 11). In the presence of hydrolysable metal ions, kaolinite and quartz powder have two ieps. As the cationic valence increases, the zeta potential of kaolinite and quartz powder becomes less negative. Monovalent cation, K+, yields more negative zeta potential values than the divalent cation Ba2+. As concentration of solid increases, the zeta potential of the minerals becomes more positive under acidic conditions; however, under alkaline conditions as solid concentration increases the zeta potential becomes more negative. Hydrated ionic radius also affects the zeta potential; the larger the ion, the thicker the layer and the more negative zeta potential for both kaolinite and quartz powder.