The present invention relates generally to a dielectric tube for use as a reflectron lens in a time of flight mass spectrometer, and more particularly, to a glass tube having a conductive surface for use as a reflectron lens in a time of flight mass spectrometer.
Time of Flight Mass Spectrometry (TOF-MS) is rapidly becoming the most popular method of mass separation in analytical chemistry. This technique is easily deployed, can produce very high mass resolution, and can be adapted for use with many forms of sample introduction and ionization. Unlike quadrupoles and ion traps, time of flight mass analyzers perform well at very high mass. Descriptions of described time of flight analyzers maybe found in Wiley and McLaren (Rec. Sci. Instrum., 26, 1150 (1950)), Cotter (Anal. Chem., 1027A (1992)), and Wollnik (Mass Spectrom Rev., 12, 89 (1993)).
Time of flight mass spectrometers are produced in two main configurations: linear instruments and reflectron instruments. In operation of either configuration of mass spectrometer an unknown sample is converted to ions. For example, a sample may be ionized using a MALDI (Matrix Assisted Laser Desorption Ionization) instrument 100, as illustrated in
t2=m/z (d2/2Vse), (1)
where m/z is the mass to charge ratio of the ion, d is the distance to the detector 20, and Vse is the acceleration potential. The lighter ions (low mass) travel faster than the higher mass ions and therefor arrive at the detector 20 earlier than the higher mass ions. If the flight tube 10 is long enough, the arrival times of all of the ions at the detector will be distributed according to mass with the lowest mass ions arriving first, as shown in
When the ions arrive at the detector 20, e.g., a multi-channel plate detector, the ions initiate a cascade of secondary electrons, which results in the generation of very fast voltage pulses that are correlated to the arrival of the ions. A high-speed oscilloscope or transient recorder maybe used to record the arrival times. Knowing the exact arrival times, equation (1) can be used to solve for the mass to charge ratio, m/z, of the ions.
The second type of time of flight mass spectrometer is a reflectron instrument 300 as shown in
The reflectron instrument 300 includes a reflectron analyzer 350 comprising a flight tube 310, reflectron lens 330, and a detector 320. The flight tube 310 includes a first, input end 315 at which the detector 320 is located and a second, reflectron end 317 at which the reflectron lens 330 is located. The ions are injected into the flight tube 310 at the input end 315 in a similar manner as a linear instrument. However, rather than detecting the ions at the opposing second end 317 of the flight tube 310, the ions are reflected back to the input end 315 of the flight tube 310 by the reflectron lens 330 where the ions are detected. As shown in
The reflection of the ions is effected by the action of an electric field gradient created by the reflectron lens 330 along the lens axis. Ions traveling down the flight tube 310 enter the reflectron lens 330 at a first end 340 of the reflectron lens 330. The electrostatic field created by applying separate high voltage potentials to each of a series of metal rings 332 of the lens 330, slows the forward progress of the ions and eventually reverses the direction of the ions to travel back towards the first end 340 of the lens 330. The ions then exit the lens 330 and are directed to the detector 320 at the first end 315 of the flight tube 310. The precision ground metal rings 332 are stacked in layers with insulating spacers 334 in between the metal ring layers. The rings 332 and spacers 334 are held together with threaded rods. This assembly may have hundreds of components which must be carefully assembled (typically by hand) in a clean, dust free environment. Such a lens assembly having many discrete components can be costly and complicated to fabricate. Moreover, the use of discrete metal rings 332 necessitates the use of a voltage divider at each layer of rings 332 in order to produce the electrostatic field gradient necessary to reverse the direction of the ions.
Accordingly, it would be an advance in the state of the art to provide a reflectron lens having a continuous conductive surface and which could introduce an electric field gradient without the use of multiple voltage dividers.
In response to the above needs, the present invention provides a reflectron lens for use in a reflectron analyzer. The reflectron lens comprises a tube having a continuous conductive surface along the length of the tube for providing an electric field interior to the tube that varies in strength along the length of the tube. The tube may comprise glass, and in particular, a glass comprising metal ions, such as lead, which may be reduced to form the conductive surface. In one configuration of the present invention, the conductive surface may be the interior surface of the tube. The tube may comprise a ceramic material and the conductive surface a glass coating on the ceramic material.
The present invention also provides a method for reflecting a beam of ions. The method includes a step of introducing a beam of ions into a first end of a dielectric tube having a continuous conductive surface along the length of the tube. The method further includes a step of applying an electric potential across the tube to create an electric field gradient that varies in strength along the length of the tube so that the electric field deflects the ions to cause the ions to exit the tube through the first end of the tube.
The foregoing summary and the following detailed description of the preferred embodiments of the present invention will be best understood when read in conjunction with the appended drawings, in which:
Referring now to
Reflectron lenses in accordance with the present invention may desirably be fabricated from a dielectric material. For example, the reflectron lens 500 may comprise a glass, such as a lead silicate glass. Examples of suitable glasses for use in reflectron lenses of the present invention include BURLE Electro-Optics Inc (Sturbridge Mass., USA) glasses MCP-10, MCP-12, MCP-9, RGS 7412, RGS 6512, RGS 6641, as well as Corning Glass Works (Corning N.Y., USA) glass composition 8161 and General Electric glass composition 821. Other alkali doped lead silicate glasses may also be suitable. In addition, non-silicate glasses may be used. Generally, any glass susceptible to treatment that modifies at least one surface of the glass tube to create a conducting surface on the glass tube, such as a hydrogen reduction treatment, is suitable for use in the present invention. Non-lead glasses may also be used, so long as the glass contains at least one constituent that may be modified to provide a conducting surface on the glass tube. Alternatively, the reflectron lens 500 may comprise a non-glass tube onto which a glass layer is deposited. Such a glass layer should be deposited on the surface of the reflectron lens 500 which is to be conductive.
A selected glass surface, or all glass surfaces, of the reflectron lens 500 is processed to make the glass surface(s) conductive. In one desirable configuration, the inside surface 510 of the reflectron lens 500 is subjected to a hydrogen reduction process. In this process, a metal oxide in the glass, such as lead oxide, is chemically reduced to a semi-conductive form. A hydrogen reduction process used to make alkali doped lead silicate glass electrically conductive is described by Trap (HJL) in an article published in ACTA Electronica (vol. 14 no 1, pp. 41–77 (1971)), for example. Changing the parameters of the reduction process can vary the electrical conductivity.
The hydrogen reduction process comprises loading the glass tube into a closed furnace through which pure hydrogen or a controlled mixture of hydrogen and oxygen is purged. The temperature is gradually increased, typically at a rate of 1–3 degrees C. per minute. Beginning at approximately 250° C., a chemical reaction occurs in the glass in which a metal oxide in the glass, such as lead oxide, is converted (reduced) to a conductive state. This reaction typically occurs in the first few hundred Angstroms of the surface. Continued heating and exposure to hydrogen produces more reduced metal oxide, which further lowers the resistance along the reflectron lens 500. Temperature, time, pressure and gas flow are all used to tailor the resistance of the conductive surface to the desired application. The soak temperature is selected to be sufficiently high to cause reduction of the metal oxide. The maximum soak temperature is selected to be below the sag point of the glass. If desired, unwanted portions of conductive surfaces can be stripped by chemical or mechanical means.
In operation, a voltage is applied across the reflectron lens 500 from end to end. The conductive inside surface 510 of the reflectron lens 500 produces an electric field gradient along the longitudinal axis of the reflectron lens 500. The field gradient produced by the continuous conductive inside surface 510 causes the ion beam to gradually reverse direction as opposed to the stepwise direction changes caused by a conventional reflectron lens. The smooth, non-stepwise action of the reflectron lens 500 of the present invention permits improved beam confinement, enabling a smaller area detector to be used. Improved ion energy dispersion reduction also results from the use of the reflectron lens 500 of the present invention. A reduction in ion energy dispersion and improved ion beam confinement leads to improved sensitivity and mass resolution in an instrument using a reflectron lens 500 of the present invention.
Reflectron lenses 600,650 of the present invention were fabricated from lead glass tubes of BURLE MCP-10 glass. The first reflectron lens 600 had the following physical dimensions: length of 3.862 inches; inner diameter of 2.40 inches; and, an outer diameter of 2.922 inches. The second reflectron lens 650 had the following physical dimensions: length of 6.250 inches; inner diameter of 1.200 inches; and, outer diameter of 1.635 inches.
The reflectron lenses 600,650 were placed in a hydrogen atmosphere at a pressure of 34 psi and a hydrogen flow of 40 l/m. The lenses 600, 650 were heated in the hydrogen atmosphere according to the following schedule. The temperature was ramped from room temperature to 200° C. over 3 hours. The temperature was then ramped to 300° C. over 1 hour, and then was ramped to 445° C. over 12.5 hours. The tube was held at 445° C. for 3 hours. The end to end resistance of the first reflectron lens 600 was measured to be 2.9×109 ohms, and the end to end resistance of the second reflectron lens 650 was measured to be 3.0×109 ohms.
These and other advantages of the present invention will be apparent to those skilled in the art from the foregoing specification. Accordingly, it will be recognized by those skilled in the art that changes or modifications may be made to the above-described embodiments without departing from the broad inventive concepts of the invention. It should therefore be understood that this invention is not limited to the particular embodiments described herein, but is intended to include all changes and modifications that are within the scope and spirit of the invention as set forth in the claims.
This application claims priority under 35 U.S.C. §119(e) from U.S. Provisional Application No. 60/455,801, filed Mar. 19, 2003, which is incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
2841729 | Wiley | Jul 1958 | A |
3197663 | Norman et al. | Jul 1965 | A |
3424909 | Rougeot | Jan 1969 | A |
3488509 | Goodrich | Jan 1970 | A |
3519870 | Jensen | Jul 1970 | A |
3634712 | Orthuber | Jan 1972 | A |
3673449 | Eschard | Jun 1972 | A |
3675063 | Spindt et al. | Jul 1972 | A |
3885180 | Carts, Jr. | May 1975 | A |
3902089 | Beasley et al. | Aug 1975 | A |
3911167 | Linder | Oct 1975 | A |
3914517 | Pirooz | Oct 1975 | A |
3959038 | Gutierrez et al. | May 1976 | A |
3976905 | Seidman et al. | Aug 1976 | A |
4015159 | Zipfel, Jr. | Mar 1977 | A |
4051403 | Feingold et al. | Sep 1977 | A |
4073989 | Wainer | Feb 1978 | A |
4093562 | Kishimoto | Jun 1978 | A |
4095136 | Niklas | Jun 1978 | A |
4099079 | Knapp | Jul 1978 | A |
4217489 | Rosier | Aug 1980 | A |
4236073 | Martin | Nov 1980 | A |
4267442 | Rosier | May 1981 | A |
4352985 | Martin | Oct 1982 | A |
4454422 | Persyk | Jun 1984 | A |
4468420 | Kawahara et al. | Aug 1984 | A |
RE31847 | Luckey | Mar 1985 | E |
4558144 | Fay et al. | Dec 1985 | A |
4563250 | Becker et al. | Jan 1986 | A |
4577133 | Wilson | Mar 1986 | A |
4589952 | Behringer et al. | May 1986 | A |
4624736 | Gee et al. | Nov 1986 | A |
4624739 | Nixon et al. | Nov 1986 | A |
4659429 | Isaacson et al. | Apr 1987 | A |
4693781 | Leung et al. | Sep 1987 | A |
4698129 | Puretz et al. | Oct 1987 | A |
4707218 | Giammarco et al. | Nov 1987 | A |
4714861 | Tosswill | Dec 1987 | A |
4725332 | Spohr | Feb 1988 | A |
4731559 | Eschard | Mar 1988 | A |
4734158 | Gillis | Mar 1988 | A |
4740267 | Knauer et al. | Apr 1988 | A |
4764245 | Grewal | Aug 1988 | A |
4780395 | Saito et al. | Oct 1988 | A |
4786361 | Sekine et al. | Nov 1988 | A |
4790903 | Sugano et al. | Dec 1988 | A |
4794296 | Warde et al. | Dec 1988 | A |
4800263 | Dillon et al. | Jan 1989 | A |
4802951 | Clark et al. | Feb 1989 | A |
4806827 | Eschard | Feb 1989 | A |
4825118 | Kyushima | Apr 1989 | A |
5086248 | Horton et al. | Feb 1992 | A |
5205902 | Horton et al. | Apr 1993 | A |
5351332 | Cook | Sep 1994 | A |
5378960 | Tasker et al. | Jan 1995 | A |
5726076 | Tasker et al. | Mar 1998 | A |
6008491 | Smentkowski et al. | Dec 1999 | A |
6369383 | Cornish et al. | Apr 2002 | B1 |
6607414 | Cornish et al. | Aug 2003 | B1 |
6717135 | Hansen | Apr 2004 | B1 |
6825474 | Young | Nov 2004 | B1 |
20030230726 | Van der Veer et al. | Dec 2003 | A1 |
Number | Date | Country |
---|---|---|
1121858 | Apr 1982 | CA |
0704879 | Apr 1996 | EP |
2180986 | Apr 1987 | GB |
Number | Date | Country | |
---|---|---|---|
20040183028 A1 | Sep 2004 | US |
Number | Date | Country | |
---|---|---|---|
60455801 | Mar 2003 | US |