Dielectric analysis on phase transition and micelle shape of polyoxyethylene trisiloxane surfactant in dilute aqueous solution

2011 ◽  
Vol 22 (6) ◽  
pp. 745-748 ◽  
Author(s):  
Ya Wen Zhou ◽  
Wei Zhou ◽  
Fu Han ◽  
Bao Cai Xu
1984 ◽  
Vol 62 (1) ◽  
pp. 56-63 ◽  
Author(s):  
O. Desrosiers ◽  
T. Van Dinter ◽  
J. K. Saunders

The 13C chemical shift, T1 and 2H T1 data for 2-butoxyethanol (BE) in D2O as a function of concentration are presented. The nmr parameters are consistent with thermodynamic data for the same system in that it appears that 2-butoxyethanol in water undergoes a pseudo phase transition at about 1.2 M. The chemical shift for each carbon is different in the microphase relative to either aqueous solution or pure BE. The shift differences are due to a combination of factors, conformer population changes, changes in the polarity of the oxygen, and a solvent effect on chemical shift. The more organic the medium, the higher the population of trans relative to gauche conformers. The motion of BE is more restricted in the microphase than in either dilute aqueous solution or in the pure liquid. The number of adsorbed D2O molecules per molecule of BE is less in the microphase than in aqueous solution.


2003 ◽  
Vol 68 (8) ◽  
pp. 1407-1419 ◽  
Author(s):  
Claudio Fontanesi ◽  
Roberto Andreoli ◽  
Luca Benedetti ◽  
Roberto Giovanardi ◽  
Paolo Ferrarini

The kinetics of the liquid-like → solid-like 2D phase transition of adenine adsorbed at the Hg/aqueous solution interface is studied. Attention is focused on the effect of temperature on the rate of phase change; an increase in temperature is found to cause a decrease of transition rate.


1968 ◽  
Vol 17 (3) ◽  
pp. 354-355 ◽  
Author(s):  
Atsushi MIZUIKE ◽  
Shigeki KANO

1965 ◽  
Vol 18 (5) ◽  
pp. 651 ◽  
Author(s):  
RW Green ◽  
PW Alexander

The Schiff base, N-n-butylsalicylideneimine, extracts more than 99.8% beryllium into toluene from dilute aqueous solution. The distribution of beryllium has been studied in the pH range 5-13 and is discussed in terms of the several complex equilibria in aqueous solution. The stability constants of the complexes formed between beryllium and the Schiff base are log β1 11.1 and log β2 20.4, and the distribution coefficient of the bis complex is 550. Over most of the pH range, hydrolysis of the Be2+ ion competes with complex formation and provides a means of measuring the hydrolysis constants. They are for the reactions: Be(H2O)42+ ↔ 2H+ + Be(H2O)2(OH)2, log*β2 - 13.65; Be(H2O)42+ ↔ 3H+ + Be(H2O)(OH)3-, log*β3 -24.11.


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