Determination of phase transition temperatures of polymer binding agents by differential scanning calorimetry

2015 ◽  
Vol 8 (1) ◽  
pp. 17-21 ◽  
Author(s):  
G. V. Malysheva ◽  
E. Sh. Akhmetova ◽  
Yu. Yu. Shimina
1980 ◽  
Vol 35 (1) ◽  
pp. 98-102 ◽  
Author(s):  
P. Franzosini ◽  
M. Sanesi ◽  
A. Cingolani ◽  
P. Ferloni

Abstract The phase transition temperatures and enthalpies were determined by differential scanning calorimetry between room temperature and the isotropic liquid region for the lithium n.alkanoates from tridecanoate to eicosanoate. The number and nature of the phases involved were discussed in comparison with the literature data available for some of the homologues concerned. For diffe-rent kinds of transitions, the significant features of the plots AS vs. number of carbon atoms were put into evidence.


2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
S. Sreehari Sastry ◽  
B. Gowri Sankara Rao ◽  
K. B. Mahalakshmi ◽  
K. Mallika ◽  
C. Nageswara Rao ◽  
...  

Phase transition temperatures of ferroelectric liquid crystals ((S)-(-)-2-methylbutyl 4′-(4″-n-alkanoyloxybenzoyloxy) biphenyl-4-carboxylates (where n=16 and 18)) are studied through two techniques of image analysis. One is a statistical method, applied to compute the statistical parameters from the textures of each sample and the other, computation of Legendre moments being applied as image moment analysis, both of which are considered as a function of temperature. The textures of the samples are recorded with the polarizing optical microscope (POM) attached to the hot stage and high resolution camera. The phase transition temperatures of samples are inferred by the abrupt changes in the computed parameter values. The results obtained from the present methodology are in good agreement with those published in earlier literature done by the different techniques, like differential scanning calorimetry (DSC).


Volume 1 ◽  
2004 ◽  
Author(s):  
Adrian S. Sabau ◽  
Wallace D. Porter

Differential Scanning Calorimetry (DSC) measurements are routinely used to determine enthalpies of phase change, phase transition temperatures, glass transition temperatures, and heat capacities. In order to obtain data on the amount of phases during phase change, time-temperature lags, which are inherent to the measurement process, must be estimated through a computational analysis. An analytical model is proposed for the systematic error of the instrument. Numerical simulation results are compared against experimental data obtained at different heating and cooling rates.


2010 ◽  
Vol 663-665 ◽  
pp. 759-762 ◽  
Author(s):  
Qing Lan Ma ◽  
Yuan Ming Huang

A series of cholesterol liquid crystal compounds was synthesized. Phase-transition temperatures and mesomorphic textures of these synthesized compounds were characterized with differential scanning calorimetry and polarized optical microscopy, respectively. In these molecules the terminal ester chains CnH2n-1COO-, where n was the number of carbon atoms in the terminal ester chains, were linked to the cholesterol core. All of the synthesized cholesterol compounds exhibited mesophases for the first heating. However, as temperature decreased from their clearing points, their micrographs can also be divided into two categories, the first category exhibits branch-like mesophase textures for n in the range of 1-10 while the second category exhibits branch-like crystal textures for n in the range of 11-18.


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