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Surface tension is one of the fundamental properties of the colloids, which can be altered by concentration and size of colloidal particles. In the current work, modeling of the surface tension of suspension as it would be analyzed by maximum bubble pressure method has been performed. A new modified equation to correlate the surface tension with the bubble pressure is derived by applying fundamental thermodynamic relation considering the presence of particles in suspension and curvature of the interface between the particles and bubbles inside liquid. Moreover, the change of particles concentration in air-water interface due to capillary force is also considered. The predicted surface tension using the developed model has been verified by numerous experimental data with deviation less than 5% in most of cases. It was found that the calculated surface tension is altered by contact angle and particle radius as well as particle concentration. The obtained model may have potential application to predict the surface tension of colloidal suspension. [ABSTRACT FROM AUTHOR]

A new generalised model of the electrowetting of microfluids has been proposed. Instead of the conventional Young-Lippmann formula, dynamic minimising of the total energy of system which is superposition of capillary free energy and electric energy has been utilised to calculate the contact angle as indicator of wetting behaviour. The change of interfacial energy of liquid/solid interface and change in relative permittivity of solution in the presence of colloid particles have also been considered in the developed model. The model predicts that contact angle saturation decreases in the presence of colloid particles both in DC and AC conditions. The model also predicts that the reduction of contact angle by applying potential is higher in the case of TiO2/water microfluidic system which is in agreement with experimental data reported in literature. [ABSTRACT FROM AUTHOR]

In order to understand the physics behind the surface properties and nano-scale phenomena, we are motivated first to investigate the inner bond strengths as well as the effect of number of neighboring atoms and their relative distance in addition to space positions (crystallography). Therefore, in order to study the effect of the nature of metallic bond on their physico-chemical properties, we first tried to investigate and introduce a mathematical model for transforming the bulk molar cohesion energy into microscopic bond strengths between atoms. Then an algorithm for estimating the nature of bond type including the materials properties and lattice scale "cutoff" has been proposed. This leads to a new fundamental energy scale free from the crystallography and number of atoms. The results of our model in case of fundamental energy scale of metals not only perfectly describe the inter relation between binding and melting phenomena but also adequately reproduce the bond strength for different bond types with respect to other estimations reported in literatures. The generalized algorithm and calculation methodology introduced here by us are suggested to be used for developing energy scale of bulk crystal materials to explain or predict any particular materials properties related to bond strengths of metallic elements. [ABSTRACT FROM AUTHOR]

In order to understand the physics behind the surface properties and nano-scale phenomena, we are motivated first to investigate the inner bond strengths as well as the effect of number of neighboring atoms and their relative distance in addition to space positions (crystallography). Therefore, in order to study the effect of the nature of metallic bond on their physico-chemical properties, we first tried to investigate and introduce a mathematical model for transforming the bulk molar cohesion energy into microscopic bond strengths between atoms. Then an algorithm for estimating the nature of bond type including the materials properties and lattice scale "cutoff" has been proposed. This leads to a new fundamental energy scale free from the crystallography and number of atoms. The results of our model in case of fundamental energy scale of metals not only perfectly describe the inter relation between binding and melting phenomena but also adequately reproduce the bond strength for different bond types with respect to other estimations reported in literatures. The generalized algorithm and calculation methodology introduced here by us are suggested to be used for developing energy scale of bulk crystal materials to explain or predict any particular materials properties related to bond strengths of metallic elements.