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Full-Text Articles in Physics
Microcalorimetric Study Of Nematic-To-Neat-Soap And Nematic-To-Isotropic Phase Transitions In A Lyotropic Liquid Crystal, T. S. Shin, Satyendra Kumar
Microcalorimetric Study Of Nematic-To-Neat-Soap And Nematic-To-Isotropic Phase Transitions In A Lyotropic Liquid Crystal, T. S. Shin, Satyendra Kumar
Satyendra Kumar
The results of specific-heat measurements at the nematic- (N) to-neat-soap (NS) and nematic-to-isotropic (I) phase transitions in binary mixtures of cesium-perfluoro-octanoate and water are reported. The ratio of specific-heat amplitudes above and below the N-NS transition, A+/A-, and the specific-heat exponent α remain ∼1.0 and ≤0.02, respectively, suggesting 3D XY-type behavior. At the first-order N-I transition, vanishing latent heat and coexistence range at low concentration indicate the existence of a Landau point.
Self-Assembly, Condensation, And Order In Aqueous Lyotropic Chromonic Liquid Crystals Crowded With Additives, Luana Tortora, Heung-Shik Park, Shin-Woong Kang, Victoria Savaryn, Seung-Ho Hong, Konstantine Kaznatcheev, Daniele Finotello, Samuel Sprunt, Satyendra Kumar, Oleg Lavrentovich
Self-Assembly, Condensation, And Order In Aqueous Lyotropic Chromonic Liquid Crystals Crowded With Additives, Luana Tortora, Heung-Shik Park, Shin-Woong Kang, Victoria Savaryn, Seung-Ho Hong, Konstantine Kaznatcheev, Daniele Finotello, Samuel Sprunt, Satyendra Kumar, Oleg Lavrentovich
Satyendra Kumar
Dense multicomponent systems with macromolecules and small solutes attract a broad research interest as they mimic the molecularly crowded cellular interiors. The additives can condense and align the macromolecules, but they do not change the degree of covalentpolymerization. We chose a lyotropic chromonic liquid crystal with reversibly and non-covalently assembled aggregates as a much softer system, reminiscent of “living polymers”, to demonstrate that small neutral and charged additives cause condensation of aggregates with ensuing orientational and positional ordering and nontrivial morphologies of phase separation, such as tactoids and toroids of the nematic and hexagonal columnar phase coexisting with the isotropic …
Novel Examples Of Achiral Bent-Core Azo Compounds Exhibiting B1 And Anticlinic-Antiferroelectric B2 Mesophases, Veena Prasad, Shin-Woong Kang, Satyendra Kumar
Novel Examples Of Achiral Bent-Core Azo Compounds Exhibiting B1 And Anticlinic-Antiferroelectric B2 Mesophases, Veena Prasad, Shin-Woong Kang, Satyendra Kumar
Satyendra Kumar
The first examples of achiral bent-core molecules consisting of an azo linkage and five aromatic rings exhibiting bent-core mesophases are reported. They exhibit B1 and B2 phases as identified by optical microscopy, differential scanning calorimetry, X-ray diffraction, and electro-optical techniques. The B2 phase of these materials is identified to be the anticlinic–antiferroelectric, SmCAPA phase. The mesophases of these compounds have relatively low transition temperatures and wide temperature ranges. The observation of bent-core phases in azo compounds assumes significance from the fact that the introduction of the –NN– linkage adds a new dimension, namely photochromism, to this field.
Relaxation Dynamics Of Rubbed Polystyrene Thin Films, D. M. G. Agra, A. D. Schwab, J-H. Kim, Satyendra Kumar, A. Dhinojwala
Relaxation Dynamics Of Rubbed Polystyrene Thin Films, D. M. G. Agra, A. D. Schwab, J-H. Kim, Satyendra Kumar, A. Dhinojwala
Satyendra Kumar
Optical retardation measurements were used to probe the chain relaxation dynamics in rubbed polystyrene films of varying thicknesses on glass substrates. A model based on Kohlrausch-Williams-Watts relaxation was developed and used to determine the glass transition temperature (Tg) of the films. Results showed reductions of 15–20 K in Tg for thin films of thicknesses comparable to the radius of gyration as well as for cast films rubbed with different strengths. These results provide evidence of a faster relaxation dynamics relative to the polymer-substrate interface for thinner films and enhanced chain mobility at the polymer-air interface.