Related Experiment Video
Updated: Jul 17, 2025

Multiscale Sampling of a Heterogeneous Water/Metal Catalyst Interface using Density Functional Theory and Force-Field Molecular Dynamics
Published on: April 12, 2019
Dissolution mechanism of Fe3O4 scale by 1-hydroxyethane-1,1-diphosphonic acid: an ab initio molecular metadynamics
Xiaoyang Zhao1, Guo Jin2, Ding Guo1
1School of Geomatic and Environmental Engineering, Henan Polytechnic Institute, Nanyang 473000, P. R. China.
Abstract:
Using the ab initio molecular metadynamics method, the adsorption of the structure of 1-hydroxyethane-1,1-diphosphonic acid (HEDP) on the Fe3O4 surface and subsequent detachment of Fe atoms from the surface were simulated, and the dissolution mechanism by which HEDP dissolves Fe3O4 scale at room temperature while other organic acids cannot was elucidated. The adsorbed hydroxyl groups, water and HEDP on the Fe3O4 surface play a synergistic role in detaching the Fe ions, which increases the coordination number of the Fe atoms and weakens the original Fe-O bond strength. In addition, the strong coordination ability and flexible molecular structure of HEDP also facilitate dissolution of Fe3O4 scale by breaking down the chemical bonds and forming Fe-HEDP complexes. The free energy surface for the dissolution reaction shows a low barrier, and the descaling reaction is easily accomplished.
Related Concept Videos
Leveling Effect and Non-Aqueous Acid-Base Solutions
The Leveling Effect of a Solvent
A generic acid (HA) reacts with the generic base (B-) to yield the corresponding conjugate base (A-) and conjugate acid (HB):
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
Theories of Dissolution: The Danckwerts' Model and Interfacial Barrier Model

