A normal incidence, vacuum ultraviolet, spectrograph/monochromator for time resolved plasma spectroscopy

1976 ◽  
Vol 9 (5) ◽  
pp. 333-334 ◽  
Author(s):  
R S Turnbull ◽  
R Illingworth
Keyword(s):  
Vacuum Ultraviolet ◽  
Normal Incidence ◽  
Plasma Spectroscopy ◽  
Time Resolved

Comparison between Intensified Photodiode Array and Charge-Coupled Device Detectors in the Vacuum Ultraviolet for Laser-Induced Plasma Spectroscopy

2001 ◽  
Vol 55 (10) ◽  
pp. 1430-1433 ◽  
Author(s):  
Mohamed A. Khater ◽  
Paul Van Kampen ◽  
John T. Costello ◽  
Jean-Paul Mosnier ◽  
Eugene T. Kennedy
Keyword(s):  
Vacuum Ultraviolet ◽  
Plasma Spectroscopy ◽  
Charge Coupled Device ◽  
Laser Induced Plasma ◽  
Photodiode Array

Microanalysis by Laser-Induced Plasma Spectroscopy in the Vacuum Ultraviolet

2004 ◽  
Vol 76 (6) ◽  
pp. 1648-1656 ◽  
Author(s):  
Igor Radivojevic ◽  
Christoph Haisch ◽  
Reinhard Niessner ◽  
Stefan Florek ◽  
Helmut Becker-Ross ◽  
...  
Keyword(s):  
Vacuum Ultraviolet ◽  
Plasma Spectroscopy ◽  
Laser Induced Plasma

scholarly journals Tracking ground state Ba+ions in an expanding laser–plasma plume using time-resolved vacuum ultraviolet photoionization imaging

2004 ◽  
Vol 22 (3) ◽  
pp. 207-213 ◽  
Author(s):  
J.S. HIRSCH ◽  
K.D. KAVANAGH ◽  
E.T. KENNEDY ◽  
J.T. COSTELLO ◽  
P. NICOLOSI ◽  
...  
Keyword(s):  
Spatial Distribution ◽  
Laser Plasma ◽  
Ground State ◽  
Column Density ◽  
Vacuum Ultraviolet ◽  
Plasma Plume ◽  
Experimental System ◽  
Time Resolved ◽  
Density Maps ◽  
Ccd Array

We report results from a study of the integrated column density and expansion dynamics of ground-state-selected Ba+ions in a laser–plasma plume using a new experimental system—VPIF (vacuum-ultraviolet photoabsorption imaging facility). The ions are tracked by recording the attenuation of a pulsed and collimated vacuum ultraviolet beam, tuned to the 5p–6dinner-shell resonance of singly ionized barium, as the expanding plasma plume moves across it. The attenuated beam is allowed to fall on a CCD array where the spatial distribution of the absorption is recorded. Time-resolved ion velocity and integrated column density maps are readily extracted from the photoionization images.

Kinetic Studies of Atomic Carbon, C[2p2 (3PJ)], with Thiols by Time-Resolved Atomic Resonance Absorption Spectroscopy in the Vacuum Ultraviolet

2005 ◽  
Vol 30 (1-2) ◽  
pp. 115-125 ◽  
Author(s):  
Mahendra P. Deeyamulla ◽  
David Husain
Keyword(s):  
Vacuum Ultraviolet ◽  
Dimethyl Sulfide ◽  
Kinetic Studies ◽  
Reaction Rates ◽  
Atomic Spectroscopy ◽  
Atomic Carbon ◽  
Time Resolved ◽  
Sulfur Containing ◽  
Electronic Ground ◽  
Pulsed Irradiation

Reaction rates of atomic carbon in its electronic ground state, C[2p2 (3PJ)], with a range of large sulfur-containing molecules have been investigated using time-resolved atomic spectroscopy in the vacuum ultraviolet following pulsed irradiation. Absolute rate data for the collisional removal at 300 K of C(23PJ) by the gases 1-propanethiol, 1-butanethiol, 1-pentanethiol, 2-propanethiol, 2-methyl-1-propanethiol, 2-methyl-2-propanethiol and dimethyl sulfide are reported. All processes proceed at rates of the order of the collision numbers, supporting an overall mechanism of C-atom insertion into the S–H bond following initial addition, which is energetically favourable, a mechanism demonstrated analogously hitherto with H2S and where H-atom abstraction would also be endothermic.

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