NOTICE: Due to a lapse in annual appropriations, most of this website is not being updated. Learn more.
Form submissions will still be accepted but will not receive responses at this time. Sections of this site for programs using non-appropriated funds (such as NVLAP) or those that are excepted from the shutdown (such as CHIPS and NVD) will continue to be updated.
An official website of the United States government
Here’s how you know
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
Secure .gov websites use HTTPS
A lock (
) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.
Dissolution and Reprecipitation of Barium at the Particulate BaTiO3-Aqueous Solution Interface
Published
Author(s)
U Paik, M Lee, Vincent A. Hackley, Y S. Jung
Abstract
The electrolinetic behavior of BaTO3 particles in an aqueous medium exhibit a hysteresis loop with titration direction. As BaTiO3 suspension was titrated toward acidic pH, the amount of Ba2+ dissolution strongly increases, and in the subsequent titration toward alkaline pH, Ba2+ adsorbed and/or reprecipitated on the Ba-depleted BaTiO3 surface. This dissolution-reprecipitation cycle results in the observed hysteresis behavior. An attempt was made to identify the responsible species of the adsorbed/reprecipitated compound by XPS in conjunction with electrokinetic titrations.
Paik, U.
, Lee, M.
, Hackley, V.
and Jung, Y.
(2002),
Dissolution and Reprecipitation of Barium at the Particulate BaTiO<sub>3</sub>-Aqueous Solution Interface, Materials Research Bulletin
(Accessed October 16, 2025)