Cathode-ray tube cathode and alloy therefor

Electric lamp and discharge devices – Electrode and shield structures – Cathodes containing and/or coated with electron emissive...

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C313S337000, C313S355000, C313S270000, C313S341000, C216S041000, C216S090000, C216S100000

Reexamination Certificate

active

06798128

ABSTRACT:

The invention relates to cathode-ray tube oxide cathodes, used as sources of electrons emitted by the thermionic effect, and more particularly to the composition of the metal forming the basis of the cathode.
BACKGROUND OF THE INVENTION
A conventional oxide cathode consists of a layer of alkaline-earth oxides, such as a mixture of barium oxide (BaO), strontium oxide (SrO) and calcium oxide (CaO) or a mixture of BaO and SrO, which is deposited on a basis metal made of nickel or a nickel alloy and comprising one or more reducing elements, such as magnesium (Mg), aluminium (Al), silicon (Si), chromium (Cr), zirconium (Zr) or any other element capable of reducing oxides. The alkaline-earth oxide mixture may itself be doped with other oxides, such as, for example, Sc
2
O
3
and Y
2
O
3
.
A conventional oxide cathode is constructed of a tube made of a Ni alloy (generally Ni—Cr) to which a cap made in the basis metal is welded. Deposited on the basis metal is a layer made of a mixture of Ba and Sr carbonates or a mixture of Ba, Sr and Ca carbonates. These carbonates, which are stable in air, are subsequently converted to oxides in the vacuum inside the cathode-ray tube. This oxide layer, heated to a cathode working temperature of approximately 800° C., becomes the electron-emitting layer when some of the BaO is converted to barium metal.
The formation of barium metal is maintained by the following mechanisms; the cathode, during operation, is heated to a temperature of approximately 800° C., causing the reducing elements to diffuse towards the interface between the nickel and the alkaline-earth oxides. These reducing elements, for example, Mg, Al and Si, constantly react with the barium oxide and reduce it, in order to form barium metal according to the reactions:
The reducing elements added to the nickel are therefore consumed by the chemical oxidation-reduction reactions with BaO. The lifetime of the cathode is directly connected with the consumption of these elements so that, for each of the addition reducing elements chosen, a minimum content is desirable in order to guarantee a minimum lifetime. Furthermore, it is known that some of the compounds resulting from the Ba reduction reactions described above, such as Ba
2
SiO
4
or BaAl
2
O
4
, are so highly stable that they can accumulate at the interface [A. Eisenstein, H. John et al., J. Appl. Phys., T.24, No. 5, p. 631, 1953] between the nickel and the alkaline-earth oxides. These compounds, because of their high resistivity, increase the impedance of the interface, thereby reducing the current density of the cathode. In addition, they degrade the lifetime of the cathode because they permanently accumulate at the interface during operation of the cathode. By accumulating, they limit the diffusion of the reducing elements and thus decrease the reactions between the latter and BaO, which in turn reduces the amount of Ba metal formed, which is necessary for emission [E. S. Rittner, Philips Res. Rep., T.8, p.184, 1953]. Another major drawback is that an excessively high accumulation of these compounds may degrade the adhesion of the alkaline-earth oxides to the nickel.
The invention aims to avoid these drawbacks by properly choosing a composition of the material forming the basis of the cathode, which material consists of a nickel alloy for which the content of reducing elements must be chosen within a defined weight concentration range according to the elements in question. Each reducing element is added to the nickel in a concentration range defined by a lower limit and an upper limit, which range guarantees a long lifetime as well as optimum emission performance and reliability. To achieve this result, the metal alloy according to the invention, intended for the manufacture of cathodes for cathode-ray tubes, mainly comprises nickel, together with magnesium (Mg), the weight concentration C
Mg
of which is between 0.01% and 0.1%. Advantageously, it also includes aluminium, the weight concentration C
Al
of which satisfies the relationship:
C
Al
≦0.14×(0.1−C
Mg
),
where:
C
mg
is the Mg concentration in the nickel expressed as a percentage by weight;
C
Al
is the Al concentration in the nickel expressed as a percentage by weight.


REFERENCES:
patent: 4184100 (1980-01-01), Takanashi et al.
patent: 4215180 (1980-07-01), Misumi et al.
patent: 4376009 (1983-03-01), Kunz
patent: 4382206 (1983-05-01), Kumada et al.
patent: 4441957 (1984-04-01), Poff et al.
patent: 4536259 (1985-08-01), Oda et al.
patent: 4636681 (1987-01-01), Misumi
patent: 4820954 (1989-04-01), Kimura et al.
patent: 4849066 (1989-07-01), Deal et al.
patent: 4904896 (1990-02-01), Chiang
patent: 4924137 (1990-05-01), Watanabe et al.
patent: 5220238 (1993-06-01), Lee
patent: 5900692 (1999-05-01), Jung et al.
patent: 6124666 (2000-09-01), Saito et al.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Cathode-ray tube cathode and alloy therefor does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Cathode-ray tube cathode and alloy therefor, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Cathode-ray tube cathode and alloy therefor will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-3253406

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.