Calorimetry dynamic

Other PDMS—sihca-based hybrids have been reported (16,17) and related to the ceramer hybrids (10—12,17). Using differential scanning calorimetry, dynamic mechanical analysis, and saxs, the microstmcture of these PDMS hybrids was determined to be microphase-separated, in that the polysiUcate domains (of ca 3 nm in diameter) behave as network cross-link junctions dispersed within the PDMS oligomer-rich phase. The distance between these... 

MODULATED TEMPERATURE DIFFERENTIAL SCANNING CALORIMETRY/DYNAMIC DIFFERENTIAL SCANNING CALORIMETRY... 

Tg can be measured by dilatometry, refractive index, differential scanning calorimetry, dynamic mechanical methods and by dielectric relaxation techniques. 

Differential Scanning Calorimetry Dynamic (10 C/min., 0 500 psig) Differential Thermal Analysis 1-3 mg 50 °C... 

The glass-transition temperature, melting point, heat distortion temperature, thermal degradation temperature, ete. are important parameters affecting the application and processing of semicrystalline polymer materials. These thermal parameters can be obtained via differential scanning calorimetry, dynamic mechanical analysis, thermogravimetric analysis, etc. 

Wang and co-workers [4] have discussed the thermal stability of PDMS-urethane copolymers using a combination of differential scanning calorimetry, dynamic mechanical analysis and cone calorimetry. 

Thermal analysis is well suited for characterizing and identifying plastics, as their properties are temperature dependent. It involves methods in which the substance is subjected to a controlled temperature program and the changes in the physical and chemical properties are measured as a function of temperature or time. The ambient atmosphere also influences the properties of plastic. Thermal analysis comprises traditional techniques differential scanning calorimetry (DSC), differential thermal analysis, thermogravimetric analysis, thermomechanical analysis, and more recent methods pressure differential scanning calorimetry, dynamic mechanical analysis, and differential photocalorimetry. 

The mechanical, thermal, and dielectric properties of sisal fiber have been studied in detail. X-ray diffraction, Infrared Spectroscopy, Thermal Gravimetric Analysis, Scanning Electron Microscopy, Differential Scanning Calorimetry, Dynamic Mechanical Analysis etc., have been used to determine the characteristics of sisal fiber and provide theoretical support for processing and application of the fiber. 

A novel process for the preparation of latex with high solid content, but maintaining the characteristics of microemulsion polymerisation latex, small particle size (less than 50 nm) and polymer with high molecular weight (more than 10 6) is presented. With the PS latex obtained by microemulsion polymerisation as seed, core shell, styrene-butyl acrylate polymers functionalised with itaconic acid are prepared. Materials were characterised by differential scanning calorimetry, dynamic mechanical thermal analysis and transmission electron microscopy. These polymers have better mechanical properties than the non functionalised or those prepared by emulsion polymerisation. 11 refs. 

Abstract The miscibility behavior in blends of polyethersulfone (Victrex PES) with the polyimide PI 2080, (the condensation product of 3,3, 4,4 -benzophenone tetracarboxylic dianhydride [BDTA] and a 4 1 mixture of 2,4-toluene diisocyanate and 4,4 -diphenylmethane diisocyanate) or with the polyimide XU 218 (the condensation product of BDTA and 5(6)-amino-l-(4 -aminophenyl)-l,3,3 -trimethylindane) was investigated using differential scanning calorimetry, dynamic mechanical analysis and thcmiogravimetric analysis. The effects of solvents (dimethylacetamide, tetramethylene sulfone, dimethyl sulfoxide and l-methyl-2-pyrrolidone) on miscibility were studied and one solvent, tetramethylene sulfone was found to have a plasticizing effect. In the absence of solvent, the equilibrium phase boundary for these blends was in the experimentally inaccessable region below the Tg-composition line. The phase boundary at zero solvent concentration was obtained by extrapolation using data collected in the presence of the plasticizer. 

Because of the link between Tg and the mechanical and thermal properties, the dependence of the glass transition temperature on blend composition is of much interest and has been the subject of many experimental and theoretical papers. The subject is particularly vast since TgS can be determined using various experimental techniques, including differential scanning calorimetry, dynamic mechanical thermal analysis, and dielectric relaxation spectroscopy (DRS). 

---