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Abstract Surface Light Scattering Spectroscopy (SLSS) can characterize the dynamics of an interface between two immiscible fluids by measuring the frequency spectrum of coherent light scattered from thermophysical fluctuations—‘ripplons’. In principle, and for many interfaces, SLSS can simultaneously measure surface tension and viscosity, with the potential for higher-order properties, such as surface elasticity and bending moments. Previously, this has been challenging. We describe and present some measurements from an instrument with improvements in optical design, specimen access, vibrational stability, signal-to-noise ratio, electronics, and data processing. Quantitative improvements include total internal reflection at the interface to enhance the typically available signal by a factor of order 40 and optical improvements that minimize adverse effects of sloshing induced by external vibrations. Information retrieval is based on a comprehensive surface response function, an instrument function, which compensates for real geometrical and optical limitations, and processing of almost real-time data to report results and their likely accuracy. Detailed models may be fit to the power spectrum in real time. The raw one-dimensional digitized data stream is archived to allow post-experiment processing. This paper reports a system design and implementation that offers substantial improvements in accuracy, simplicity, ease of use, and cost. The presented data are for systems in regions of low viscosity where the ripplons are underdamped, but the hardware described is more widely applicable. 

Research on colloids is motivated by several factors. They can be used to answer fundamental questions related to the assembly of materials, and they have many potential applications in electronics, photonics, and life sciences. However, the rich variety of colloidal structures observed on the Earth can be influenced by the effects of gravity, which leads to particles settling and the motion of the surrounding fluid. To suppress the gravity effects, experiments on concentrated colloids of spherical and ellipsoidal fluorescent particles were carried out aboard the International Space Station. The particles were suspended in a decalin/tetralin mixture to match the particle refractive index. Confocal microscopy was used to visualize the particle behavior. The work was supported by the NSF CBET grants 1832260 and 1832291 and the NASA grant 80NSSC19K1655. 

Research on colloids is motivated by several factors. They can be used to answer fundamental questions related to the assembly of materials, and they have many potential applications in electronics, photonics, and life sciences. However, the rich variety of colloidal structures observed on the Earth can be influenced by the effects of gravity, which leads to particles settling and the motion of the surrounding fluid. To suppress the gravity effects, experiments on concentrated colloids of spherical and ellipsoidal fluorescent particles were carried out aboard the International Space Station. The particles were suspended in a decalin/tetralin mixture to match the particle refractive index. Confocal microscopy was used to visualize the particle behavior. The work was supported by the NSF CBET grants 1832260 and 1832291 and the NASA grant 80NSSC19K1655. 

The organization of multiple subcellular compartments is controlled by liquid–liquid phase separation. Phase separation of this type occurs with the emergence of interfacial tension. Aqueous two-phase systems formed by two non-ionic polymers can be used to separate and analyze biological macromolecules, cells and viruses. Phase separation in these systems may serve as the simple model of phase separation in cells also occurring in aqueous media. To better understand liquid–liquid phase separation mechanisms, interfacial tension was measured in aqueous two-phase systems formed by dextran and polyethylene glycol and by polyethylene glycol and sodium sulfate in the presence of different additives. Interfacial tension values depend on differences between the solvent properties of the coexisting phases, estimated experimentally by parameters representing dipole–dipole, ion–dipole, ion–ion, and hydrogen bonding interactions. Based on both current and literature data, we propose a mechanism for phase separation in aqueous two-phase systems. This mechanism is based on the fundamental role of intermolecular forces. Although it remains to be confirmed, it is possible that these may underlie all liquid–liquid phase separation processes in biology.