scholarly journals Swelling of iota-carrageenan gels prepared with various CaCl2 content: A fluorescence study

e-Polymers ◽  
2008 ◽  
Vol 8 (1) ◽  
Author(s):  
Özlem Tarı ◽  
Önder Pekcan

AbstractIota carrageenan gels prepared with various CaCl2 content were completely dried and then swelled in water vapor. Steady-state fluorescence (SSF) technique was used to monitor the swelling process of each iota carrageenan gels at various temperatures. Pyranine was used as a fluorescence probe. Apparent fluorescence intensity, I increased as swelling time increased for all gel samples. The increase in I was modelled using Li-Tanaka equation from which the swelling time constants, τ1 and cooperative diffusion coefficients, Dc were determined. It was observed that Dc increased as the swelling temperature was increased. On the other hand at each temperature, it was seen that Dc decreased as CaCl2 content was increased. Activation energies for swelling were obtained and found to be 60.5, 61.0, 61.5 and 62.8 kJmol-1 for the gels prepared with increasing amount of CaCl2 content.

1996 ◽  
Vol 50 (6) ◽  
pp. 740-746 ◽  
Author(s):  
Ming Li ◽  
Frank V. Bright

A steady-state fluorescence study of low-molecular-weight polystyrene (MW = 1060 g/mol and 13,000 g/mol) plasticized in supercritical CO2 is reported. In addition to excitation wavelength, molecular weight, and polystyrene concentration dependencies, CO2 density also strongly affects the emission spectral contours. A major increase in the steady-state fluorescence intensity and a significant decrease in the polystyrene 320- to 365-nm fluorescence intensity ratio are observed when CO2 density is increased. Concentration and conformational changes in the polystyrene molecules are used to explain the observations, and these results are proposed to arise from changes in the plasticization power of supercritical CO2 over the density range studied. A theoretical model is proposed that is based on the assumption that, at low CO2 densities and low polymer concentrations, polystyrene intermolecular interactions are negligible. The proposed model is able to fit our observed fluorescence data from a CO2 reduced density of 0.3 to 1.4.


2001 ◽  
Vol 17 (09) ◽  
pp. 828-831 ◽  
Author(s):  
Fang Yun ◽  
◽  
Liu Xue-Feng ◽  
Xia Yong-Mei ◽  
Yang Yang ◽  
...  

2005 ◽  
Vol 109 (12) ◽  
pp. 2840-2846 ◽  
Author(s):  
Angel Orte ◽  
Ruperto Bermejo ◽  
Eva M. Talavera ◽  
Luis Crovetto ◽  
Jose M. Alvarez-Pez

1993 ◽  
Vol 2 (2) ◽  
pp. 149-151 ◽  
Author(s):  
A. Kantar ◽  
P. L. Giorgi ◽  
R. Fiorini

The effect of PAF on the plasma membrane polarity of polymorphonuclear leukocytes (PMNs) was investigated by measuring the steady-state fluorescence emission spectra of 2-dimethylamino(6-1auroyl) naphthalene (Laurdan), which is known to be incorporated at the hydrophobic-hydrophilic interface of the bilayer, displaying spectral sensitivity to the polarity of its surrounding. Laurdan shows a marked steady-state emission blue-shift in non-polar solvents, with respect to polar solvents. Our results demonstrate that PAF (10−7M) induces a blue shift of the fluorescence emission spectra of Laurdan. These changes are blocked in the presence of the PAF antagonist, L-659,989. Our data indicate that the interaction between PAF and PMNs is accompanied by a decrease in polarity in the hydrophobic-hydrophilic interface of the plasma membrane.


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