Application of Extended DLVO Theory: Modeling of Flotation and Hydrophobicity of Dodecane

The extended DLVO theory was used to develop a flotation model by considering both hydrodynamic and surface forces involved in the process. A stream function was used to estimate the kinetic energies for thinning the water films between bubbles and particles, which were compared with the energy barriers, created by surface forces, to determine the probability of adhesion. A general expression for the probability of detachment was derived from similar mechanism for chemical reaction, and the kinetic energy for detachment was estimated with French and Wilson's model. The hydrophobic force parameter (K132) calculated from the rate constants of single bubble flotation tests showed that, K132 for bubble-particle interaction were close to the geometric means of K131 for particle-particle interactions and K232 for bubble-bubble interaction, indicating that the combining rules developed for dispersion forces may be useful for hydrophobic forces. The model was used to predict flotation results as functions of several important parameters such as contact angle, double-layer potentials, particle size, bubble size, etc. The predictions were consistent with experience, and could be explained in view of the various subprocesses considered in the model development. Furthermore, the model suggested optimum conditions for achieving the maximum separation efficiency. The extended DLVO theory was also used to determine the hydrophobic force between two oil/solution interfaces from the equilibrium film thicknesses of dodecylammonium chloride (RNH3Cl) solutions obtained using Thin Film Balance (TFB) technique. The results showed that, the oil droplets were inherently hydrophobic, and the hydrophobic force played an important role in the stability of emulsions. This force decreased with increasing surfactant concentration, and also changed with pH and the addition of electrolyte. The interfacial area occupied by molecules indicated that, the dodecane molecules might present between two surfactant ions at interface, thus the hydrophobicity of oil/solution interface was less sensitive to the addition of the surfactant than that of air/solution interface. Thermodynamic analysis suggested that, there might exist a relationship between the interfacial hydrophobicity and the interfacial tension.

Name thesis:degree_name

Ph. D.

Level thesis:degree_level

doctoral

Discipline thesis:degree_discipline

Mining and Minerals Engineering

Department dc:contributor.department

Mining and Minerals Engineering

Grantor dc:publisher

Virginia Tech

Year dc:date.issued

1998

Author dc:creator

• Mao, Laiqun

Chair dc:contributor.committeechair

• Yoon, Roe-Hoan

Committee members dc:contributor.committeemember

• Xu, Zhenghe
• Davis, Richey M.
• Adel, Gregory T.
• Luttrell, Gerald H.

• Dodecane
• Flotation Modeling
• Extended DLVO theory
• Hydrophobic Force

Statement dc:rights

• In Copyright

Licence dc:rights.uri

• http://rightsstatements.org/vocab/InC/1.0/

Dc Identifier Other

etd-100998-123843

OAI identifier oai:identifier

oai:vtechworks.lib.vt.edu:10919/29232