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Abstract Studying the behavior of anisotropic particles at fluid interfaces is a rapidly expanding field, as understanding how the introduced anisotropy affects the resulting properties is essential in the engineering of interfacial systems. Surface anisotropic particles, also known as Janus particles (JPs), offer new possibilities for novel applications due to their amphiphilicity and stronger binding to fluid interfaces compared to homogeneous particles. Introducing surface anisotropy creates complexity as the orientation of interfacially bound particles affects interparticle interactions, a contributing factor to the microstructure formation. In this work, we have investigated the microstructure of JP monolayers formed at the air–water interface using particles with different degrees of amphiphilicity and examined the response of the networks to applied compressions. Our findings demonstrate that JPs amphiphilicity is a crucial factor governing their orientation at the interface, which in turn dictates the complexity of the capillary interactions present and the mechanical properties of the ensuing networks. 

The behavior of colloidal particles near fluid interfaces has attracted significant scientific interest, as particles minimize the contact area between the two fluid phases, stabilizing interfacial systems. This study explores the influence of surface roughness on the properties of particle monolayers at the air–water interface, focusing on colloidal silica particles and fumed silica particles of similar hydrodynamic diameter. This research involves comparing low-surface-area (LSA) and medium-surface-area (MSA) fumed silica particles with spherical colloidal silica particles (250 nm in diameter). Utilizing a Langmuir trough, the interfacial particle networks are compressed and expanded. Analysis of surface pressure isotherms reveals that fumed silica particle monolayers form networks at a lower particle surface coverage compared to spherical particles. The spherical particle monolayer exhibits a higher apparent surface elasticity, indicating greater resistance to the applied compression compared to fumed silica networks. Additionally, monolayers formed by fumed silica particles display hysteresis even after successive compressions and expansions due to irreversible particle interlocking and the formation of multilayered aggregates. These findings provide insights into the impact of surface roughness on the behavior of particle monolayers at fluid interfaces, offering valuable information for designing and optimizing mechanisms involved in emulsion and foam stabilization. 

Abstract Interfacial rheology studies were conducted to establish a connection between the rheological characteristics of particle-laden interfaces and the stability of Pickering foams. The behavior of foams stabilized with fumed and spherical colloidal silica particles was investigated, focusing on foam properties such as bubble microstructure and liquid content. Compared to a sodium dodecyl sulfate-stabilized foam, Pickering foams exhibited a notable reduction in bubble coarsening. Drop shape tensiometry measurements on particle-coated interfaces indicated that the Gibbs stability criterion was satisfied for both particle types at various surface coverages, supporting the observed arrested bubble coarsening in particle-stabilized foams. However, although the overall foam height was similar for both particle types, foams stabilized with fumed silica particles demonstrated a higher resistance to liquid drainage. This difference was attributed to the higher yield strain of interfacial networks formed by fumed silica particles, as compared to those formed by spherical colloidal particles at similar surface pressures. Our findings highlight that while both particles can generate long-lasting foams, the resulting Pickering foams may exhibit variations in microstructure, liquid content, and resistance to destabilization mechanisms, stemming from the respective interfacial rheological properties in each case.