Interfacial Behaviour in Ferroalloys: The Influence of Sulfur in FeMn and SiMn Systems

The present study has investigated the influence of sulfur content in synthetic FeMn and SiMn from 0 to 1.00 wt pct on interfacial properties between these ferroalloys and slags. The effect of experimental parameters such as temperature and holding time was evaluated. Interfacial interaction between ferroalloys and slags was characterized by interfacial tension and apparent contact angle between metal and slag, measured based on the Young–Laplace equation and an inverse modelling approach developed in OpenFOAM. The results show that sulfur has a significant influence on both interfacial tension and apparent contact angle, decreasing both values and promoting the formation of a metal-slag mixture. Despite the fact that sulfur was added only to the ferroalloys, most of sulfur is distributed into slag after reactions with the metal phase. Increasing the maximum experimental temperature in the sessile drop furnace also resulted in a decrease of both interfacial properties, resulting in higher mass transfer rates and intensive reactions between metal and slag. The effect of holding time demonstrated that after reaching equilibrium in FeMn-slag and SiMn-slag systems (both with and without sulfur), interfacial tension and apparent contact angle remain constant.

Motion of water monomers reveals a kinetic barrier to ice nucleation on graphene

The interfacial behaviour of water remains a central question to fields as diverse as protein folding, friction and ice formation. While the properties of water at interfaces differ from those in the bulk, major gaps in our knowledge limit our understanding at the molecular level. Information concerning the microscopic motion of water comes mostly from computation and, on an atomic scale, is largely unexplored by experiment. Here, we provide a detailed insight into the behaviour of water monomers on a graphene surface. The motion displays remarkably strong signatures of cooperative behaviour due to repulsive forces between the monomers, enhancing the monomer lifetime ( ≈ 3 s at 125 K) in a free-gas phase that precedes the nucleation of ice islands and, in turn, provides the opportunity for our experiments to be performed. Our results give a molecular perspective on a kinetic barrier to ice nucleation, providing routes to understand and control the processes involved in ice formation.