Supersonic jet spectrometry of chemical species resulting from thermal decomposition of polystyrene and polycarbonate

1992 ◽  
Vol 64 (19) ◽  
pp. 931A-940A ◽  
Author(s):  
Totaro Imasaka ◽  
Masami Hozumi ◽  
Nobuhiko Ishibashi
1992 ◽  
Vol 64 (19) ◽  
pp. 2206-2209 ◽  
Author(s):  
Totaro. Imasaka ◽  
Masami. Hozumi ◽  
Nobuhiko. Ishibashi

2003 ◽  
Vol 75 (7) ◽  
pp. 975-998 ◽  
Author(s):  
Totaro Imasaka ◽  
D. S. Moore ◽  
T. Vo-Dinh

When cooled to a temperature of a few K using supersonic jet expansion into a vacuum, a molecule exists in the lowest vibrational level of the ground electronic state and is isolated at collision-free conditions. The absorption or excitation/fluorescence spectrum is then greatly simplified, when transitions occur from this single vibrational level to a limited number of vibrational levels in the excited electronic state. This method, called supersonic jet spectrometry, is a powerful analytical technique because of its high selectivity, since the chemical species can be accurately identified and selectively quantified using the sharp spectral features even for large molecules. Supersonic jet spectrometry has distinct advantages over other low-temperature spectrometries,in that it can be combined with gas-phase separation and detection techniques such as chromatography or mass spectrometry. Therefore, this spectrometric technique can be used as a versatile analytical means, not only for basic research on pure substances, but also for practical trace analysis of chemical species in multicomponent samples (e.g., in biological monitoring or in environmental monitoring).


2010 ◽  
Vol 176 (1-3) ◽  
pp. 575-578 ◽  
Author(s):  
Ilaria Di Somma ◽  
Antonino Pollio ◽  
Gabriele Pinto ◽  
Maria De Falco ◽  
Elio Pizzo ◽  
...  

Author(s):  
C. S. Chen ◽  
M. M. El-Wakil

This paper presents an experimental and theoretical study of the self-ignition and burning behaviour of drops of hydrocarbon mixtures. In the experimental work, the mass histories, as well as temperature, shape, and flame histories, of drops of heavy hydrocarbon mixtures, suspended on fine thermocouple beads and subjected to heated air streams, were obtained. Due to thermal decomposition and irregular burning, the masses could not be determined from temperature and size and were measured by a liquid-nitrogen quenching technique. Temperature, flame, and shape histories were obtained in the usual manner by thermocouple and photographic means. Drops of grade 6 fuel oil and grade 6 fuel oil minus its asphaltene constituent, of 1·2 and 1·7 mg initial mass, subjected to 1450 and 1600°F air-stream temperatures, were studied. The drop histories can be divided into four phases: (1) pre-ignition, (2) self-ignition and combustion, (3) thermal decomposition, and (4) carbon residue, or cenosphere, burning. The asphaltenes contributed a great deal to burning irregularities but not to burning rates or temperatures. The latter were higher the higher the air temperature, but were affected less by changes in air velocity. In the theoretical work, a generalized treatment predicting the histories of drops undergoing unsteady vaporization, burning, thermal decomposition, or combinations of these was formulated. Based on a spherically symmetric model, governing equations of state, continuity, chemical species conservation, and energy conservation were solved with the aid of simplifying assumptions. A computer program was developed covering a wide range of operating conditions. The theoretical model showed reasonable agreement with the experimental results. A universal plot estimating drop histories of heavy residual fuels was prepared. The distribution of the total heat input into sensible heat, latent heat of vaporization, and endothermic heat of decomposition was also plotted versus dimensionless time.


1989 ◽  
Vol 61 (14) ◽  
pp. 1530-1533 ◽  
Author(s):  
Totaro. Imasaka ◽  
Kouji. Tashiro ◽  
Nobuhiko. Ishibashi

Author(s):  
R. H. Duff

A material irradiated with electrons emits x-rays having energies characteristic of the elements present. Chemical combination between elements results in a small shift of the peak energies of these characteristic x-rays because chemical bonds between different elements have different energies. The energy differences of the characteristic x-rays resulting from valence electron transitions can be used to identify the chemical species present and to obtain information about the chemical bond itself. Although these peak-energy shifts have been well known for a number of years, their use for chemical-species identification in small volumes of material was not realized until the development of the electron microprobe.


Author(s):  
William J. Baxter

In this form of electron microscopy, photoelectrons emitted from a metal by ultraviolet radiation are accelerated and imaged onto a fluorescent screen by conventional electron optics. image contrast is determined by spatial variations in the intensity of the photoemission. The dominant source of contrast is due to changes in the photoelectric work function, between surfaces of different crystalline orientation, or different chemical composition. Topographical variations produce a relatively weak contrast due to shadowing and edge effects.Since the photoelectrons originate from the surface layers (e.g. ∼5-10 nm for metals), photoelectron microscopy is surface sensitive. Thus to see the microstructure of a metal the thin layer (∼3 nm) of surface oxide must be removed, either by ion bombardment or by thermal decomposition in the vacuum of the microscope.


Sign in / Sign up

Export Citation Format

Share Document