Reevaluation of the ultrasonic absorption spectra of aqueous samarium(III) sulfate solutions

1975 ◽  
Vol 79 (19) ◽  
pp. 1995-1999 ◽  
Author(s):  
Michael M. Farrow ◽  
Neil Purdie ◽  
Edward M. Eyring
Keyword(s):  
Absorption Spectra ◽  
Ultrasonic Absorption ◽  
Sulfate Solutions

Ultrasonic absorption spectra of vanadium benzohydroxamic acid in 1-butanol

1977 ◽  
Vol 49 (6) ◽  
pp. 881-882
Author(s):  
A. Ford ◽  
I. Wakabayashi ◽  
C. E. Meloan
Keyword(s):  
Absorption Spectra ◽  
Ultrasonic Absorption ◽  
Benzohydroxamic Acid

Ultrasonic Absorption in Magnesium Sulfate Solutions

1953 ◽  
Vol 25 (4) ◽  
pp. 658-660 ◽  
Author(s):  
Philip L. Connolly ◽  
Francis E. Fox
Keyword(s):  
Magnesium Sulfate ◽  
Ultrasonic Absorption ◽  
Sulfate Solutions

scholarly journals Analysis and Kinetic Interpretation of Ultrasonic Absorption Spectra.

1969 ◽  
Vol 23 ◽  
pp. 1007-1016 ◽  
Author(s):  
Jørgen Rassing ◽  
Hans Lassen ◽  
H. Lid ◽  
Carl-Gunnar Lindblad ◽  
Alf A. Lindberg ◽  
...  
Keyword(s):  
Absorption Spectra ◽  
Ultrasonic Absorption

Ultraviolet Absorption of Refractory Elements by a Dual Laser Plasma Method

1988 ◽  
Vol 102 ◽  
pp. 243-246
Author(s):  
J.T. Costello ◽  
W.G. Lynam ◽  
P.K. Carroll
Keyword(s):  
Absorption Spectra ◽  
Laser Plasma ◽  
Optical Pulse ◽  
Ionic Species ◽  
Neutral Species ◽  
Plasma Method ◽  
Plasma Technique ◽  
Refractory Elements ◽  
Delay Times ◽  
Dual Laser

AbstractThe dual laser-produced plasma technique for the study of ionic absorption spectra has been developed by the use of two Q-switched ruby lasers to enable independent generation of the absorbing and back-lighting plasmas. Optical pulse handling is used in the coupling cicuits to enable reproducible pulse delays from 250 nsec. to 10 msec, to be achieved. At delay times > 700 nsec. spectra of essentially pure neutral species are observed. The technique is valuable, not only for obtaining the neutral spectra of highly refractory and/or corrosive materials but also for studying behaviour of ionic species as a function of time. Typical spectra are shown in Fig. 1.

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