1. Technical Field
The invention relates to vacuum gauges and, particularly, to an ionization vacuum gauge employed with carbon nanotubes.
2. Description of Related Art
Ionization vacuum gauges have been used for several years. The conventional ionization vacuum gauge includes a cathode, an anode surrounding the cathode, and an ion collector surrounding the anode. The cathode, the anode and the ion collector are separated from one another so as to not to be in direct electrical contact with each other. In operation, electrons emitted from the cathode travel towards and through the anode and eventually are collected by the ion collector. In their travels, electrons may collide with the molecules and atoms of gas in the vacuum system. Thus, ions may be produced, and collected by the ion collector. As is well known, the pressure of the vacuum system can be calculated by the formula P=(1/k)(Iion/Ielectron), wherein k is a constant with the unit of 1/torr and is a parameter of a particular gauge geometry and electrical parameters, Iion is a current of the ion collector, and Ielectron is a current of the anode.
In the process described above, some electrons may collide with the anode when the electrons travel though the anode and cause the anode to emit X rays. A virtual current Ix may be produced when the X ray irradiates the ion collector. The virtual current Ix will produce a virtual pressure Px which will affect the sensitivity of the ionization vacuum gauge. As is well known, the value of Px can be calculated by the formula Px=(1/k)(Ix/Ielectron). And, the pressure of the vacuum system measured by ionization vacuum gauges is Pm, and Pm=P+Px. As such, the greater the value of Ix is, the less sensitive the ionization vacuum gauges have. As is well known, the value of Ix is related to the atomic number of the anode material, and the greater the atomic number of the anode material, the greater the value of Ix. However, the anode material of the conventional ionization vacuum gauge is metal, which has a relatively high atomic number so as that the virtual current Ix may have a greater value. Therefore, the conventional ionization vacuum gauge tends to be unsuitable for high vacuum systems that are sensitive to temperature and/or light and/or that have extremely high vacuum levels.
What is needed, therefore, is an ionization vacuum gauge that has a small value of virtual current and is suitable for being used in the high vacuum systems.
Many aspects of the present ionization vacuum gauge can be better understood with reference to the following drawings. The components in the drawings are not necessarily to scale, the emphasis instead being placed upon clearly illustrating the principles of the present ionization vacuum gauge.
Corresponding reference characters indicate corresponding parts throughout the several views. The exemplifications set out herein illustrate at least one preferred embodiment of the ionization vacuum gauge.
Reference will now be made to the drawings to describe in detail embodiments of the present ionization vacuum gauge.
Referring to
The ionization vacuum gauge 100 further includes a housing 120 and three leads 122. The housing 120 may be part of a vacuum system in which the linear cathode 102, the helix anode 104, and the ion collector 106 are contained. The housing 120 is connected to a chamber (not shown) whose pressure is to be determined. The three leads 122 are electrically connected to the linear cathode 102, the helix anode 104, and the ion collector 106, respectively. It is to be understood that the vacuum system can incorporate one or more known evacuation mechanisms (not shown), as needed to achieve the desired level of vacuum.
The linear cathode 102 may be a hot cathode or a cold electrode. In the present embodiment, the linear cathode 102 is a cold electrode. The linear cathode 102 includes a linear core 108 and a field emission film 110 coated on the linear core 108. The linear core 108 is an electric conductive element, such as oxidation-resistant metal thread made, e.g., of nickel (Ni), tungsten (W), or copper (Cu). A diameter of the linear core 108 is in a range from about 0.2 mm to about 2 mm. In this embodiment, the diameter is about 0.3 mm. The field emission film 110 mainly consists of carbons, metal, or silicon dioxide. In the present embodiment, the field emission film 110 is composed of carbon nanotubes, low-melting-point glass powders, conductive particles, and an organic carrier/binder. The weight percents of the foregoing ingredients are respectively: about 5%˜15% of carbon nanotubes, about 10%˜20% of conductive particles, about 5% of low-melting-point glass powders, and about 60%˜80% of an organic carrier/binder. The organic carrier/binder will be evaporated and/or burned off in a drying step. The other three ingredients will be left in the final film composition. Carbon nanotubes can be obtained by a conventional method such as chemical vapor deposition, arc discharging, or laser ablation. In this embodiment, the carbon nanotubes are obtained by chemical vapor deposition. The carbon nanotubes have a length of from about 5 microns (μm) to about 15 μm.
A radial space exist between the linear cathode 102 and the ion collector 106 (referred to as D) is in a range from about 10 mm to about 15 mm. The ion collector 106 is made of an oxidation-resistant, conducting metal, such as aluminum (Al), copper (Cu), tungsten (W), or an alloy thereof. The ion collector 106 has an porous and/or planar structure, such as a metallic ring, a metal-enclosed aperture, a metallic net, or a metallic sheet.
A radial space “d” between the anode 104 and the linear cathode 102 is in a range from about 1 millimeter (mm) to about 8 mm. The anode 104 can be a hollow structure including a carbon nanotube wire structure.
The carbon nanotube wire structure includes carbon nanotube wires and carbon nanotube cables. The anode 104 is a helix structure. The carbon nanotube wire structure surrounds the linear cathode 102 as a helix that has the pitch of about 100 μm to about 1 cm.
The carbon nanotube wire includes a plurality of successive and oriented carbon nanotubes. The carbon nanotubes in the carbon nanotube wire are joined end to end by van der Waals attractive force. The carbon nanotube wire 30 can also be twisted or untwisted. Referring to
The carbon nanotube cable includes two or more carbon nanotube wires. The carbon nanotube wires in the carbon nanotube cable can be parallel with each other or twisted with each other. When the carbon nanotube cable can be twisted or untwisted. In an untwisted carbon nanotube cable, the carbon nanotube wires are parallel with each other. In a twisted carbon nanotube cable, the carbon nanotube wires are twisted with each other.
Referring to
The anode 204 in the second embodiment can be a carbon nanotube structure. The carbon nanotube structure can include at least one carbon nanotube film. A plurality of micropores can be formed and distributed uniformly in the carbon nanotube structure. Diameters of the micropores range from about 1 μm to about 10 μm. The anode 204 includes one carbon nanotube film or two or more than two carbon nanotube films overlapped or stacked with each other. Each carbon nanotube film includes a plurality of carbon nanotubes arranged along a same direction (e.g., collinear and/or parallel). The carbon nanotubes in the carbon nanotube film are joined by van der Waals attractive force therebetween. Referring to
When the anode 204 is cylinder, the ionization vacuum gauge 200 can further include a supporter (not shown). The supporter is configured to support the anode 204. The material of the supporter can be selected from the materials that have a low atomic number, such as beryllium (Be), boron (B) or carbon (C). The supporter may be a yarn or net, surrounding the linear cathode 202. The supporter is coaxial with the anode 204, and the anode 204 is disposed on a surface of the supporter.
The carbon nanotubes in the carbon nanotube structure can be selected from a group consisting of single-walled, double-walled, and/or multi-walled carbon nanotubes.
In operation of the ionization vacuum gauge, an electric voltage is applied between the cathode and the anode, the cathode emits electrons. The electrons are drawn and accelerated towards the anode by the electric field force, then tend to pass through the anode because of the inertia of the electrons thereof. The ion collector is supplied with a negative electric potential for decelerating the electrons. Therefore, before arriving at the ion collector, electrons are drawn back to the anode, and an electric current (Ielectron) is formed. In the travel of the electrons, electrons collide with gas molecules, and ionize some of gas molecules, and thus ions are produced in this process. Typically, the ions are in the form of positive ions and are collected by the ion collector, and, thus, an ion current (Iion) is formed. A ratio of Iion to Ielectron is proportional to the pressure in the ionization vacuum gauge, within a certain pressure range, covering the primary range of interest for most vacuum devices. Therefore, the pressure in the ionization vacuum gauge and, by extension, the vacuum device (not shown), to which it is fluidly attached, can be measured according to the above.
In the process discussed above, some electrons may collide with the anode, which causes the anode to emit X rays. A virtual current Ix may be produced when the X rays irradiates the ion collector. The virtual current Ix will affect the sensitivity of the Ionization vacuum gauge. The value of Ix is related to the atomic number of the anode material. The higher the atomic number is, the greater the value of Ix. Since the anode material of the ionization vacuum gauge comprises carbon nanotube, the atomic number is much smaller than the conventional anode material, therefore the ionization vacuum gauge is suitable for measuring high vacuum systems.
Referring to
Finally, it is to be understood that the above-described embodiments are intended to illustrate rather than limit the invention. Variations may be made to the embodiments without departing from the spirit of the invention as claimed. The above-described embodiments illustrate the scope of the invention but do not restrict the scope of the invention.
Number | Date | Country | Kind |
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2008 1 0066962 | May 2008 | CN | national |
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