|
|
|
| United States Patent | 3984727 |
| Link to this page | http://www.wikipatents.com/3984727.html |
| Inventor(s) | Young; Robert A. (R.R. No. 2, Loretto, Ontario, CA) |
| Abstract | A low power, sealed, optically thin resonance lamp having a controllable
chemical decomposition source of a triatomic gas and a chemical getter
sink in a sealed RF excited discharge. The discharge occurs in a second,
extremely pure gas which is present in great excess over the gas produced
by chemical decomposition. Excitation of species whose emission is desired
occurs by electron impact or energy transfer from the major species which
are, in turn, excited by the electron impact. |
|
|
|
Title Information  |
|
|
|
|
|
Drawing from US Patent 3984727 |
|
|
Resonance lamp having a triatomic gas source |
|
|
|
|
|
| Publication Date |
*
October 5, 1976 |
|
|
|
|
|
| Filing Date |
March 10, 1975 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Title Information  |
|
|
Description  |
|
|
This invention relates generally to resonance lamps and more particularly
to self-breakdown gas discharge lamps suitable for excitation by low
power, low voltage, radio frequency power.
Such a lamp used as either an oxygen resonance lamp or a hydrogen resonance
lamp is described in U.S. Pat. No. 3,851,214, issued Nov. 26, 1974 in the
name of the present inventor. These lamps use a source of diatomic gas.
The use of resonance absorption and fluoresence is becoming more important
in the field of chemical kinetic research.
Most lamps used to produce resonance radiation of atoms derived from
gaseous compounds utilize an AC electrical discharge in a low pressure gas
which flows away from the emission direction. Since dissociation must
coincide or preceed excitation, it is difficult to obtain bright resonance
lamps without absorption within the lamp. Such absorption decreases the
sensitivity of measuring devices using resonance lamps, and introduces
complications in relating intensity measurements to the concentration of
absorbers.
Although non-flowing, sealed resonance lamps have considerable convenience,
they are difficult to control since the discharge interacts with the walls
of the lamp to either remove or provide constituents.
Accordingly, it is an object of this invention to provide a very intense
resonance lamp which emits radiation such that direct detection of the
transmitted or scattered radiation, without the intervention of filters or
dispersal devices, can be used to measure the concentration of the
absorbing species while preserving a Doppler line profile unmodified by
absorption within the lamp.
A further object of this invention is to provide a lamp as described above
using a source of triatomic gases.
These and other objects of the invention will become apparent from the
following description when taken in conjunction with the drawings wherein;
FIG. 1 is a schematic diagram of the tube of the present invention,
FIG. 2 is a perspective view of a preferred embodiment of the present
invention, and
FIGS. 3 and 4 are perspective views of alternate embodiments of the present
invention.
Broadly speaking, the present invention utilizes a controllable chemical
decomposition source of parent species and a chemical getter sink in a
sealed RF excited discharge. This discharge occurs in a second, extremely
pure gas which is present in great excess over the gas produced by
chemical decomposition. Excitation of species whose emission is desired
occurs by electron impact or energy transfer from the major species which
are, in turn, excited by the electron impact.
Illustrated in FIG. 1 is a vacuum tight cylindrical body 11 having a glass
wall 13 and a hollow reentrant element 15. Reentrant element 15 extends
coaxially substantially the length of the cylinder. An electrical
conductor 17 is contained within the hollow reentrant element and extends
outwardly to connect to an RF energy source 18.
A first hollow arm 19 is integral with cylinder 13 and extends outwardly
therefrom. The arm is closed at the outer end and is filled with a getter
or scavenger 21 such as uranium or a barium containing compound. A gas
permeable barrier 23, such as a glass frit, in hollow arm 19 prevents the
getter from moving into the cylinder. Heating means 25 here illustrated as
an electrical heater, is provided about the arm so as to heat the getter
material if necessary.
A second arm 27 also extends from the cylinder and is closed at its outer
end. This arm contains the source 29 of the species whose emission is
desired. A barrier 31 and a heater 33 are also provided on arm 27.
Cylindrical body 13 is closed at the other end by a window 34 which is
transparent to the spectral emission of the species being examined. A
special epoxy cement may be required to attach the window to the body of
the lamp.
In order to complete the necessary path for electrical excitation, the
outside of cylinder 35 may be coated with an electrically conductive
material and this coating is grounded as shown. If the cylinder is largely
contained within a close fitting, grounded conducting enclosure, a
separate coating is not required. In either case, the cylinder is
effectively sheathed by a conductive element.
The lamp of the present invention may be used to produce emission of a
number of desired species. Examples of this are shown below.
The lamp is subjected to the usual vacuum pump down procedures and the lamp
is filled with approximately 1-10 torr of a rare gas such as Argon, Neon,
Krypton, Xenon or Helium.
One arm of the lamp is provided with a getter 21 such as Ur or Ba. The
other arm is supplied with a source of triatomic gas such as water
CO.sub.2, NO.sub.2, or SO.sub.2, for example, from sources 29 such as
CuSO.sub.4.5H.sub.2 O, BaCl.sub.2.2H.sub.2 O, BaO.sub.2.8H.sub.2 O,
CaO.sub.2.8H.sub.2 O, NaSO.sub.4.10H.sub.2 O, or PbCO.sub.3, MgCO.sub.3,
NaHCO.sub.3, ZuCO.sub.3, Ba(NO.sub.2).sub.2 or SnSO.sub.4 and similar
compounds.
For operation of the lamp, high purity is essential. The reason for this is
believed to be due to the role of the rare gas metastable excited species
which builds up in the discharge to a high concentration in the absence of
a triatomic gas from the source. With the application of heat to the
decomposition source, H.sub.2 O, CO.sub.2, NO.sub.2, So.sub.2 or other
triatomic gases are added and the following representative reaction takes
place in the presence of RF excitation at 150 to 600 megahertz.
Ar* + H.sub.2 O .fwdarw. Ar +OH* + H
oh* .fwdarw. oh and h.sub..gamma.(desired radiation)
Although the lamp is shown as cylindrical, this particular geometrical
configuration is not essential so long as the reentrant portion with the
electrode extends coaxially substantially the length of the tube. Further,
the lamp body can be of any sufficiently strong, non-porous material such
as the illustrated glass or a suitable metal.
Under some circumstances, it may be desirable to eliminate the central
element in the tube. With the central element present, the radiation
emanating through the window will include a central black spot, with a
resulting donut shaped view. Such a black spot can be avoided by
constructing the tube as shown in FIGS. 3 and 4 with the central element
eliminated and the exterior electrode split into two electrodes. Thus,
there is provided a more uniform discharge.
The tube 71 of FIG. 3 shows the face 77 opposite the window as being of a
continuous substantially flat configuration. Electrodes 78 and 79 are
mounted on the exterior of the main body of the tube in opposed
relationship. The power is supplied to electrode 78 from the RF generator
while electrode 79 is maintained at ground potential. In this tube, the
discharge occurs within the tube between the two electrodes. The arms 73
and 75 serve the same purpose as the arms described in FIGS. 1 and 2. The
circuit as illustrated acts as a series tuned circuit which includes the
RF generator, the coil, and the plate electrodes 78 and 79 which form the
capacitive elements of the circuit. Such an arrangement reduces the power
requirements for operating the lamp.
FIG. 4 discloses a further configuration of a tube 81. In this embodiment,
electrodes 83 and 85 are secured within the main body of the tube and the
RF generator is connected to electrode 85 through a glass seal 89.
Electrode 83 is also provided with the necessary connection through glass
seal 87. In operation, the tube functions the same as the tube of FIG. 3.
The above description and drawings are illustrative only since variations
in geometrical constructions and power supply could be varied without
departing from the invention. Accordingly, the invention is to be limited
only by the scope of the following claims.
* * * * *
|
|
|
|
|
Description  |
|