Soap formation in monomolecular films on aqueous solutions

1955 ◽  
Vol 51 ◽  
pp. 1154 ◽  
Author(s):  
J. A. Spink ◽  
J. V. Sanders

Historical . It has been known for some time that extensive changes occur in monomolecular films of fatty acids on aqueous solutions, as the alkalinity or acidity is varied. These changes are of at least tow kinds; changes in the packing of the molecules in the coherent types of film, and changes in the lateral adhesion between molecules have already been described. Thus Adam found changes in the packing of the molecules in the condensed films on changing from neutral to acid solution; and also a change from condensed to gaseous or vapour expanded films, on changing from natural to strongly alkaline solutions. The second of those effects was considered to be due to a decrease in the lateral adhesion between the molecules, caused by the development of similar electric charges on the end groups, through electrolytic dissociation of the carboxyl group on alkaline solutions. On alkaline solutions, it has previously been noted that the films contract spontaneously; Adam called this "solution," but did not examine it in detail; Lyons and Rideal believed it to be not a complete solution, but the formation of a bimolecular layer two molecules thick; Zocher and Stiebel, by ultramicroscopic examintion, concluded that this disappearance of the film was due to a partial collapse into thick, localized aggregates, not into a uniform bimolecular film.


This paper describes observations, mostly made in 1924 and not hitherto published in detail,* on the surface pressure of γ hydroxy-stearic acid (I) and its lactone (II) spread as monomolecular films on aqueous solutions. CH3 3 CH3 3 (CH 2 ) 13 (CH 2 ) 13 CHOH CH CH 2 CH 2 CH 2 O COOH CH 2 – CO I II Most of the measurements were made with the modification of Langmuir’s apparatus described in Parts I and II of this series of papers,† in which jets of air prevent the film passing the ends of the float. A few confirmatory observations have been made since, with the apparatus of Adam and Jessop, in which thin metallic ribbons block these gaps. The acid and lactone were kindly given me by Dr. P. W. Clutterbuck, of Manchester University.


Author(s):  
K. J. Böhm ◽  
a. E. Unger

During the last years it was shown that also by means of cryo-ultra-microtomy a good preservation of substructural details of biological material was possible. However the specimen generally was prefixed in these cases with aldehydes.Preparing ultrathin frozen sections of chemically non-prefixed material commonly was linked up to considerable technical and manual expense and the results were not always satisfying. Furthermore, it seems to be impossible to carry out cytochemical investigations by means of treating sections of unfixed biological material with aqueous solutions.We therefore tried to overcome these difficulties by preparing yeast cells (S. cerevisiae) in the following manner:


Author(s):  
S.A.C. Gould ◽  
B. Drake ◽  
C.B. Prater ◽  
A.L. Weisenhorn ◽  
S.M. Lindsay ◽  
...  

The atomic force microscope (AFM) is an instrument that can be used to image many samples of interest in biology and medicine. Images of polymerized amino acids, polyalanine and polyphenylalanine demonstrate the potential of the AFM for revealing the structure of molecules. Images of the protein fibrinogen which agree with TEM images demonstrate that the AFM can provide topographical data on larger molecules. Finally, images of DNA suggest the AFM may soon provide an easier and faster technique for DNA sequencing.The AFM consists of a microfabricated SiO2 triangular shaped cantilever with a diamond tip affixed at the elbow to act as a probe. The sample is mounted on a electronically driven piezoelectric crystal. It is then placed in contact with the tip and scanned. The topography of the surface causes minute deflections in the 100 μm long cantilever which are detected using an optical lever.


1988 ◽  
Vol 49 (7) ◽  
pp. 1271-1293 ◽  
Author(s):  
J.C. Earnshaw ◽  
R.C. McGivern ◽  
P.J. Winch

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