Differential scanning calorimetry

About: Differential scanning calorimetry is a research topic. Over the lifetime, 50315 publications have been published within this topic receiving 1152335 citations. The topic is also known as: DSC.

Crystallization in Poly(l-lactide)-b-poly(∊-caprolactone) Double Crystalline Diblock Copolymers: A Study Using X-ray Scattering, Differential Scanning Calorimetry, and Polarized Optical Microscopy

Abstract: The crystallization of well-defined poly(L-lactide)-b-poly(epsilon-caprolactone) diblock copolymers, PLLA-b-PCL, was investigated by time-resolved X-ray techniques, polarized optical microscopy (POM), and differential scanning calorimetry (DSC). Two compositions were studied that contained 44 and 60 wt % poly(L-lactide), PLLA (they are referred to as (L44C5614)-C-11 and (L60C409)-C-12, respectively, with the molecular weight of each block in kg/mol as superscript). The copolymers were found to be initially miscible in the melt according to small-angle X-ray scattering measurements (SAXS). Their thermal behavior was also indicative of samples whose crystallization proceeds from a mixed melt. Sequential isothermal crystallization from the melt at 100 degreesC (for 30 min) and then at 30 degreesC (for 15 min) was measured. At 100 degreesC only the PLLA block is capable of crystallization, and its crystallization kinetics was followed by both WAXS and DSC; comparable results were obtained that indicated an instantaneous nucleation with three-dimensional superstructures (Avrami index of approximately 3). The spherulitic nature of the superstructure was confirmed by POM. When the temperature was decreased to 30 degreesC, the PCL block was able to crystallize within the PLLA negative spherulites (with an Avrami index of 2, as opposed to 3 in homo-PCL), and its crystallization rate was much slower than an equivalent homo-PCL. Time-resolved SAXS experiments in (L60C409)-C-12 revealed an initial melt mixed morphology at 165 degreesC that upon cooling transformed into a transient microphase-separated lamellar structure prior to crystallization at 100 degreesC.

High-Temperature Behavior of CsH2PO4 under Both Ambient and High Pressure Conditions

Abstract: The high-temperature behavior of CsH₂PO₄ has been carefully examined under both ambient and high pressure (1.0 ± 0.2 GPa) conditions. Ambient pressure experiments encompassed thermal analysis, AC impedance spectroscopy, ¹H NMR spectroscopy, and polarized light microscopy. Simultaneous thermogravimetric analysis, differential scanning calorimetry, and evolved gas analysis by mass spectroscopy demonstrated that a structural transition with an enthalpy of 49.0 ± 2.5 J/g occurred at 228 ± 2 °C, just prior to thermal decomposition. The details of the decomposition pathway were highly dependent on sample surface area, however the structural transformation, a superprotonic transition, was not. Polarized light microscopy showed the high temperature phase to be optically isotropic in nature, consistent with earlier suggestions that this phase is cubic. The conductivity of CsH₂PO₄, as revealed by the impedance measurements, exhibited a sharp increase at the transition temperature, from 1.2 × 10⁻⁵ to 9.0 × 10⁻³ Ω¹⁻cm⁻¹, followed by a rapid decline due to dehydration. In addition, chemically adsorbed surface water was shown to increase the conductivity of polycrystalline CsH₂PO₄ over well-dried samples, even at mildly elevated temperatures (>200 °C). At high pressure an apparent irreversible phase transition at 150 °C and a reversible superprotonic phase transition at 260 °C were observed by impedance spectroscopy. At the superprotonic transition, the conductivity increased sharply by ~3 orders of magnitude to 3.5 × 10⁻² Ω¹⁻cm⁻¹ at 275 °C. This high conductivity phase was stable to the highest temperature examined, 375 °C, and exhibited reproducible and highly Arrhenius conduction behavior, with an activation energy for charge transport of 0.35 eV. Upon cooling, CsH₂PO₄ remained in the high-temperature phase to a temperature of 240 °C.

Physical properties of crosslinked hyaluronic acid hydrogels

Abstract: In order to improve the mechanical properties and control the degradation rate of hyaluronic acid (HA) an investigation of the structural and mechanical properties of the hydrogels crosslinked using divinyl sulfone (DVS), glutaraldehyde (GTA) and freeze-thawing, or autocrosslinking has been carried out. The thermal and mechanical properties of the gels were characterised by differential scanning calorimetry (DSC), dynamic mechanical thermal analysis (DMTA) and compression tests. The solution degradation products of each system have been analysed using size exclusion chromatography (SEC) and the Zimm-Stockmayer theory applied. Autocrosslinked gels swell the most quickly, whereas the GTA crosslinked gels swell most slowly. The stability of the autocrosslinked gels improves with a reduction in solution pH, but is still poor. GTA and DVS crosslinked gels are robust and elastic when water swollen, with glass transition values around 20 degrees C. SEC results show that the water soluble degradation products of the gels show a reduction in the radius of gyration at any particular molecular weight and this is interpreted as indicating increased hydrophobicity arising from chemical modification.

Crystallization kinetics of poly(L‐lactide) in contact with pressurized CO2

Abstract: The effect of CO 2 on the isothermal crystallization kinetics of poly(L-lactide). PLLA, was investigated using a high-pressure differential scanning calorimeter (DSC), which can perform calorimetric measurements while keeping the sample polymer in contact with pressurized CO 2 . It was found that the crystallization rate followed the Avrami equation. However, the crystallization kinetic constant was changed depending upon the crystallization temperature and concentration of CO 2 dissolved in the PLLA. The crystallization rate was accelerated by CO 2 at the temperature in the crystal-growth rate controlled region (self-diffusion controlled region), and depressed in the nucleation-controlled region. CO 2 has also decreased the glass transition temperature. T g , and the melting temperature. T m . As a result, the CO 2 -induced change in the crystallization rate can be predicted from the magnitudes of depression of both T g and the equilibrium melting temperature. The crystalline structure and crystallinity of polymers crystallized in contact with pressurized CO 2 were also investigated using a wide angle X-ray diffractometer (WAXD). The resulting crystallinity of the sample was increased with the pressure level of CO 2 , although the presence of CO 2 did not change the crystalline structure.