Salting out of neon from solutions: Relationship to the structure of the aqueous solution of an electrolyte

1974 ◽  
Vol 14 (6) ◽  
pp. 924-927
Author(s):  
A. K. Lyashchenko ◽  
A. F. Borina
Keyword(s):  
1977 ◽  
Vol 55 (23) ◽  
pp. 4018-4027 ◽  
Author(s):  
Robert Aveyard ◽  
Syed M. Saleem

An approach to the study of the influence of electrolytes on adsorbed nonelectrolytes at liquid surfaces is described. The adsorption of tetrabutylammonium bromide (Bu4NBr) from aqueous solution to the interfaces with octane, decanol, and air has been determined. Results are presented for the effects of some inorganic salts (NaCl, NH4Br, and Na2CO3), and of Bu4NBr on monolayers of butanol at the air – aqueous solution interface, and of Bu4NBr on dodecanol adsorbed at the octane – aqueous solution interface. The interfacial salt effects differ from the bulk effects in the cases studied. The inorganic salts, which salt-out butanol (and alkanols generally) in aqueous solution, have little or no effect on adsorbed butanol. On the other hand, Bu4NBr which salts-in alkanols in bulk aqueous solution has a strong salting-out effect on dodecanol at the liquid–liquid interface; a similar but less marked effect is observed for butanol at the liquid–vapour surface. Salting-in of alkanols by Bu4NBr in bulk has previously been ascribed to hydrophobic interactions between cations and alkyl groups of the alkanol, whereas the surface effect is assumed to result from interactions between alcoholic OH groups and cations.


2013 ◽  
Vol 9 ◽  
pp. 1858-1866 ◽  
Author(s):  
Hai Ming Wang ◽  
Gerhard Wenz

The formation of soluble 1:2 complexes within hydrophilic γ-cyclodextrin (γ-CD) thioethers allows to perform photodimerizations of aromatic guests under controlled, homogenous reaction conditions. The quantum yields for unsubstituted anthracene, acenaphthylene, and coumarin complexed in these γ-CD thioethers were found to be up to 10 times higher than in the non-complexed state. The configuration of the photoproduct reflected the configuration of the dimeric inclusion complex of the guest. Anti-parallel orientation of acenaphthylene within the CD cavity led to the exclusive formation of the anti photo-dimer in quantitative yield. Parallel orientation of coumarin within the complex of a CD thioether led to the formation of the syn head-to-head dimer. The degree of complexation of coumarin could be increased by employing the salting out effect.


2001 ◽  
Vol 76 (7) ◽  
pp. 757-763 ◽  
Author(s):  
Tang Zhigang ◽  
Zhou Rongqi ◽  
Duan Zhanting
Keyword(s):  

2000 ◽  
Vol 78 (2-3) ◽  
pp. 165-171 ◽  
Author(s):  
Xiaoping Lu ◽  
Pingfan Han ◽  
Yaming Zhang ◽  
Yanru Wang ◽  
Jun Shi

1986 ◽  
Vol 25 (4) ◽  
pp. 657-664 ◽  
Author(s):  
Jerzy Budz ◽  
Piotr H. Karpinski ◽  
Jerzy Mydlarz ◽  
Jaroslav Nyvlt
Keyword(s):  

2001 ◽  
Vol 192 (1-2) ◽  
pp. 1-12 ◽  
Author(s):  
Ying Guang Wu ◽  
Masaaki Tabata ◽  
Toshiyuki Takamuku ◽  
Atsushi Yamaguchi ◽  
Tomomi Kawaguchi ◽  
...  

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