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In high-resolution adiabatic scanning calorimetry (ASC) experiments, data for the temperature dependence of the specific enthalpy, h(T), and of the specific heat capacity, cp(T), are simultaneously obtained, from which the order of the phase transition and critical behaviour can be evaluated. ASC was applied to study the nematic to ferroelectric nematic phase transition (N–NF) in the liquid crystal molecule 4-[(4-nitrophenoxy)carbonyl]phenyl 2,4-dimethoxybenzoate (RM734). The N–NF was found to be very weakly first order with a latent heat Δh = 0.115 ± 0.005 J/g. The pretransitional specific heat capacity behaviour is substantially larger in the high-temperature N phase than in the low-temperature NF phase. In both phases the power-law analysis of cp(T) resulted in a critical exponent α = 0.50 ± 0.05 and amplitude ratio ANF/AN = 0.42 ± 0.03. The very small latent heat and the value of α indicate that the N–NF transition is close to a tricritical point. This is confirmed by a value of the order parameter exponent β ≈ 0.25, recently obtained from electric polarisation measurements. Invoking two-scale-factor universality, it follows from the low value of ANF/AN ratio that the size of the critical fluctuations is much larger in the NF phase than in the N phase. [ABSTRACT FROM AUTHOR]

Adiabatic scanning calorimetry was used to study four ionic liquid crystals whose phase sequences include highly ordered crystal smectic phases (crystal smectic E or T phases). The ionic liquids were based on piperidinium or morpholinium cations with long alkyl chains; the anions were tetrafluoroborate or hexafluorophosphate. High-resolution heat capacity and enthalpy data were obtained, from which the total transition heat and latent heat for the observed phase transitions were determined. All transitions displayed a non-zero latent heat and were thus found to be first order. [ABSTRACT FROM AUTHOR]

The phase transition behaviour of the chiral liquid crystal CE6 doped with spherical surface-functionalised CdSe nanoparticles has been examined by means of high-resolution adiabatic scanning calorimetry and polarising microscopy. The addition of nanoparticles results in an essentially stabilised blue phase III. The phase diagram is displayed upon heating and cooling and the enthalpy changes involved in the conversion between the blue phases are determined. The dispersion of functionalised nanoparticles is prominent for the stabilisation of blue phase III, which is potentially useful for applications, especially if applied on liquid crystals that exhibit blue phases close to room temperature. [ABSTRACT FROM AUTHOR]

High-resolution calorimetric techniques have substantially contributed in characterising and understanding the delicate thermal behaviour near many phase transitions in liquid crystals. In this paper we describe a high-resolution adiabatic scanning calorimetric technique that has proven to be an important tool in discriminating between first-order and second-order phase transitions in addition to rendering high-resolution information on fluctuations-induced pretransitional specific heat capacity behaviour. The capabilities of adiabatic scanning calorimetry are illustrated with experimental results for the isotropic to nematic and the isotropic to smectic A transitions for a series of alkylcyanobiphenyl compounds. For the nematic to smectic A transition results are presented for pure compounds and mixtures of liquid crystals as well as on the effects of added non-mesogenic solutes and nanoparticles. For chiral molecules results for phase transitions involving blue phases and twist grain boundary phases are considered. [ABSTRACT FROM AUTHOR]

We have employed high-resolution calorimetric techniques in order to investigate the unresolved issue of the existence of a nematic phase for the liquid crystal dodecylcyanobiphenyl. Various heating and cooling runs were performed on dodecylcyanobiphenyl samples of different origin and their analysis did not reveal any signature of a nematic phase. The calorimetric results are presented in detail and they are additionally supported by optical polarising microscopy observations. [ABSTRACT FROM AUTHOR]