Accelerator mass spectrometry measuring method and system

Abstract

An accelerator mass spectrometry measuring system is disclosed, including: an ECR high-current positive ion source subsystem; an injector subsystem; a high-current accelerator subsystem; a high-energy analysis subsystem; and a high-resolution detector subsystem; of which, the ECR high-current positive ion source subsystem, the injector subsystem, the high-current accelerator subsystem, high-energy analysis subsystem and a high-resolution detector subsystem are connected sequentially; the ECR high-current positive ion source subsystem is configured for generating high-current positive ions of multi-charge states; the high-current accelerator subsystem is configured for accelerating the high-current positive ions. The AMS system is high in beam, high in overall efficiency, and strong in how-down capability, and can greatly improve the abundance sensitivity of measurement.

Claims

1. An accelerator mass spectrometry measuring system, comprising: an ECR high-current positive ion source subsystem; an injector subsystem; a high-current accelerator subsystem; a high-energy analysis subsystem; and a high-resolution detector subsystem; wherein, the ECR high-current positive ion source subsystem, the injector subsystem, the high-current accelerator subsystem, high-energy analysis subsystem and a high-resolution detector subsystem are connected sequentially; the ECR high-current positive ion source subsystem is configured to process elements to generate high-current positive ions of multi-charge states; the high-current accelerator subsystem is configured for accelerating the high-current positive ions; wherein, the elements processed by the ECR high-current positive ion source subsystem comprise at least one of H to super actinide; the multi-charge states comprise charge states greater than or equal with +2; the high-current positive ions of multi-charge states do not comprise molecular ions; wherein the high-current accelerator subsystem is a high-current single stage electrostatic accelerator without a stripper.

2. The accelerator mass spectrometry measuring system of claim 1, wherein, the high-current single stage electrostatic accelerator comprising a plurality of accelerating tube units; a beam intensity of the high-current accelerator subsystem ranges from 10 μA to 100 mA.

3. The accelerator mass spectrometry measuring system of claim 1, wherein, the high-energy analysis subsystem comprises: a first magnetic analyzer, a first absorption membrane, an electrostatic analyzer and a second magnetic analyzer, the first magnetic analyzer, the first absorption membrane, the electrostatic analyzer and the second magnetic analyzer are connected in sequence; the first absorption membrane is in a stationary state or a rotating state after the high-energy analysis subsystem is started.

4. The accelerator mass spectrometry measuring system of claim 1, wherein, the high-resolution detector subsystem comprises a second absorption membrane and a high-resolution detector which are connected in sequence; the second absorption membrane is in a stationary state or in a rotating state after the high-resolution detector subsystem is activated.

5. The accelerator mass spectrometry measuring system of claim 1, wherein, the high-resolution detector subsystem is a gas detector with two cathodes and two anodes.

6. The accelerator mass spectrometry measuring system of claim 1, wherein, the injector subsystem comprises: a pre-acceleration section and a low-energy end magnetic analyzer which are connected in sequence; the low-energy magnetic analyzer is configured for selecting mass-to-charge ratio of ions to be accelerated.

7. The accelerator mass spectrometry measuring system of claim 1, further comprising: a control subsystem that is respectively connected with the ECR high-current positive ion source subsystem, the injector subsystem, the high-current accelerator subsystem, the high-energy analysis subsystem and the high-resolution detector subsystem to control operation of all subsystems.

8. An accelerator mass spectrometry measuring method comprising: generating high-current positive ions of multi-charge states by processing elements by an ECR high-current positive ion source subsystem; injecting the high-current positive ions into a high-current accelerator subsystem by an injector subsystem; wherein the high-current accelerator subsystem is a high-current single stage electrostatic accelerator without a stripper; accelerating the high-current positive ions by the high-current accelerator subsystem with an accelerating voltage corresponding to the high-current positive ions; carrying out high-energy analysis on ion beams outputted from the high-current accelerator subsystem by a high-energy analysis subsystem; detecting positive ions after high-energy analysis by a high-resolution detector subsystem; wherein, the elements processed by the ECR high-current positive ion source subsystem comprise at least one of H to super actinide; the multi-charge states comprise charge states greater than or equal with +2; the high-current positive ions of multi-charge states do not comprise molecular ions.

9. An accelerator mass spectrometry measuring system, comprising: an ECR high-current positive ion source subsystem; an injector subsystem; a high-current accelerator subsystem; a high-energy analysis subsystem; and a high-resolution detector subsystem; wherein, the ECR high-current positive ion source subsystem, the injector subsystem, the high-current accelerator subsystem, high-energy analysis subsystem and a high-resolution detector subsystem are connected sequentially; the ECR high-current positive ion source subsystem is configured to process elements to generate high-current positive ions of multi-charge states; the high-current accelerator subsystem is configured for accelerating the high-current positive ions; wherein, the elements processed by the ECR high-current positive ion source subsystem comprise at least one of H to super actinide; the multi-charge states comprise charge states greater than or equal with +2; the high-current positive ions of multi-charge states do not comprise molecular ions; the high-resolution detector subsystem is a gas detector with two cathodes and two anodes.

10. The accelerator mass spectrometry measuring system of claim 9, wherein, the high-current accelerator subsystem is a high-current single stage electrostatic accelerator, the high-current single stage electrostatic accelerator comprising a plurality of accelerating tube units; a beam intensity of the high-current accelerator subsystem ranges from 10 μA to 100 mA.

11. The accelerator mass spectrometry measuring system of claim 9, wherein, the high-energy analysis subsystem comprises: a first magnetic analyzer, a first absorption membrane, an electrostatic analyzer and a second magnetic analyzer, the first magnetic analyzer, the first absorption membrane, the electrostatic analyzer and the second magnetic analyzer are connected in sequence; the first absorption membrane is in a stationary state or a rotating state after the high-energy analysis subsystem is started.

12. The accelerator mass spectrometry measuring system of claim 9, wherein, the high-resolution detector subsystem comprises a second absorption membrane and a high-resolution detector which are connected in sequence; the second absorption membrane is in a stationary state or in a rotating state after the high-resolution detector subsystem is activated.

13. The accelerator mass spectrometry measuring system of claim 9, wherein, the injector subsystem comprises: a pre-acceleration section and a low-energy end magnetic analyzer which are connected in sequence; the low-energy magnetic analyzer is configured for selecting mass-to-charge ratio of ions to be accelerated.

14. The accelerator mass spectrometry measuring system of claim 9, further comprising: a control subsystem that is respectively connected with the ECR high-current positive ion source subsystem, the injector subsystem, the high-current accelerator subsystem, the high-energy analysis subsystem and the high-resolution detector subsystem to control operation of all subsystems.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIG. 1 is a structural diagram of the prior AMS system;

(2) FIG. 2 is a structural diagram of an accelerator mass spectrometry measuring system according to embodiments of the present disclosure;

(3) FIG. 3 is a structural diagram of an ECR high-current positive ion source according to embodiments of the present disclosure;

(4) FIG. 4 is a flow chart of an accelerator mass spectrometry measuring method according to embodiments of the present disclosure.

DESCRIPTION OF EMBODIMENTS

(5) To make the aim, purpose and advantage more understandable, a further description to the present disclosure will be laid out hereinafter.

First Embodiment

(6) With reference to FIG. 2, which is a structural diagram of an accelerator mass spectrometry measuring system according to embodiments of the present disclosure. The accelerator mass spectrometry measuring system includes:

(7) an ECR high-current positive ion source subsystem 20;

(8) an injector subsystem 21; a high-current accelerator subsystem 22;

(9) a high-energy analysis subsystem 23 and a high-resolution detector subsystem 24;

(10) the ECR high-current positive ion source subsystem 20, the injector subsystem 21, the high-current accelerator subsystem 22, the high-energy analysis subsystem 23 and the high-resolution detector subsystem 24 are connected sequentially.

(11) As shown in FIG. 2, the ECR high-current positive ion source subsystem 20 is connected with an input end of the injector subsystem 21, an output end of the injector subsystem 21 is connected with an input end of the high-current accelerator subsystem 22, an output end of the high-current accelerator subsystem 22 is connected with an input end of the high-energy analysis subsystem 23; an output end of the high-energy analysis subsystem 23 is connected with an input end of the high-resolution detector subsystem 24.

(12) Additionally, the ECR high-current positive ion source subsystem 20 is configured for generating high-current positive ions of multi-charge states.

(13) According to embodiments of the present disclosure, the ECR high-current positive ion source subsystem 20 is configured for generating high-current positive ions of multi-charge states, i.e. ions with +2, +3 etc., for instance, ions of Be.sup.2+ or Be.sup.3+.

(14) The ECR ion source heat plasmas by using microwave, electrons obtain power from the microwave to become high-energy electrons. Free atoms in the high-energy electrons generate ECR plasmas. The ECR plasmas is restrained by a magnetic field with minimum B. Therefore, the ions in the plasmas have plenty of time to be gradually separated to generate ions of high-charge state; the ions are proceeded by high voltage to form ion beams that are supplied to an accelerator. Microwaves are fed into the plasma area via a waveguide or coaxial line. When the microwave frequency ωRF is equal to the electron's cyclotron motion frequency ωce in the magnetic field, that is, ωce=ωRF=eB/me, resonance will occur and energy will be absorbed from the microwave to produce high-energy electrons. For a fixed ωRF, B is also determined. As shown in FIG. 3, which shows a structural diagram of an ECR high-current positive ion source according to embodiments of the present disclosure. The ECR high-current positive ion source in FIG. 3 includes following structures: a wire package 1, an insulation cover 2, a permanent magnet 3, an extraction electrode 4, an arc cavity 5, a plasma 6, a quartz tube, an injection cone 8, a coaxial inner tube 9, a cooling water inlet and outlet 10, a wave guide 11, an air inlet □ 12 and a microwave tube 13. As shown in FIG. 3, the wire package 1 and the permanent magnet 3 form the needed magnetic field. The microwave is fed through a microwave window and transmitted along the coaxial inner tube into the are cavity, heats the plasma, and generates ions that is further drawn out through the system. To obtain ions of high-charge state, ECR plasma must be well confined, which requires a reasonable magnetic confinement field shape. Generally, the magnetic field is a superposition of the multi-pole radial field in the axial situation. The axial field is composed of a pair of magnetic mirrors. The electrons are restricted by the magnetic mirror field and move back and forth between the magnetic mirrors, increasing the chance of being heated. The radial field is generally composed of multi-pole permanent magnets, which can confine the plasma well in a radial direction. Of course, in the embodiments of the present application, based on the principle of ECR, ECR high-current positive ion source subsystems in other structural components may also be used, which is not limited in the embodiments of the present application.

(15) Preferably, elements processed by the ECR high-current positive ion source subsystem 20 include at least one of H to Pu, actinide, and super actinide.

(16) In embodiments of the present disclosure, the elements selected from at least one of H to Pu, actinide, and super actinide, processed by the ECR high-current positive ion source subsystem 20, are capable of generating ions of multi-charge states such as +1, +2, +3, +4, etc.

(17) In embodiments of the present disclosure, the subsystem can measure .sup.10Be and .sup.14C and also measure isotopes such as .sup.3H, .sup.26Al, .sup.32Si, .sup.36Cl, .sup.41Ca, .sup.129I, U and Pu, and super actinide, more especially realize highly sensitive measurement of other inert gases such as 39Ar, .sup.85Kr and .sup.133Xe.

(18) In which, the high-current accelerator subsystem 22 is configured for accelerating high-current positive ions.

(19) In the embodiments of the present disclosure, since the injector subsystem 21 injects high-current positive ion beams, but when the ECR high-current positive ion source subsystem 20 generates high-current ions of multi-charge states such as +2, +3, +4 etc., they are positive ions, not molecular ions. Therefore, the high-current accelerator subsystem 22 may only have acceleration function without the stripper S04 in the traditional AMS. In the traditional AMS, Since it uses a sputtering negative ion source 10 as shown in FIG. 1, the negative ion source 10 would generate molecular ions when it generates negative ions. Therefore, the tandem accelerator system M12 in use must include the stripper S04, which strips the negative ions into Positive ions, and molecular ions are unstable after being stripped into positive ions, leading to dissociate, and thus may be separated.

(20) Preferably, the high-current accelerator subsystem 22 is a high-current single stage electrostatic accelerator, the high-current single stage electrostatic accelerator includes a plurality of accelerating tube units; a beam intensity of the high-current accelerator subsystem ranges from 10 μA to 100 mA.

(21) Understandable, the high-current single stage electrostatic accelerator has no gas or solid glass components, the beam intensity that can be accelerated is in the range of 10 μA˜100 mA. The high-current single stage electrostatic accelerator has no stripper with consequently simple structure, and easy to be maintained.

(22) Preferably, the accelerating voltage of the high-current accelerator subsystem 22 ranges from 0˜800 kV.

(23) There may also be a control system that controls other subsystems to work, such as controlling the accelerating voltage of the high-current accelerator subsystem 22.

(24) Preferably, in another embodiment, with reference to FIG. 2, the injector subsystem 21 includes: a pre-accelerating section A01 and a low-energy magnetic analyzer A02; the pre-accelerating section A01 and the low-energy magnetic analyzer A02 are connected in sequence. The low-energy magnetic analyzer is configured for selecting mass-to-charge ratio of the ions to be accelerated.

(25) As shown in FIG. 2, an output end of the high-current accelerator subsystem 22 is connected with an input end of the pre-accelerating section A01, an output end of the pre-accelerating section A01 is connected with an input end of the low-energy magnetic analyzer A02. The output end of the low-energy magnetic analyzer A02 is connected with the input end of the high-current accelerator subsystem 22.

(26) It needs to be illustrated, the pre-accelerating section A01 may be an accelerating tube of 20 kV˜80 kV, used for acceleration beforehand, after the ions pass through the low-energy end magnetic analyzer A02, a good mass resolution can be obtained, in which, the low-energy end magnetic analyzer A02 can be used to inject the magnet, which is used to select the mass-to-charge ratio of the ion to be accelerated, where the mass-to-charge ratio is the ratio of the mass number to the charge state. For example, if .sup.9Be.sup.3+ is selected for acceleration, its mass-to-charge ratio is 9/3.

(27) Preferably, in another embodiment, with reference to FIG. 2, the high-energy analyzer subsystem 23 includes a first magnetic analyzer A03, a first absorption membrane A04, an electrostatic analyzer A05 and a second magnetic analyzer A06; the first magnetic analyzer A03, the first absorption membrane A04, the electrostatic analyzer A05 and the second magnetic analyzer A06 are connected in sequence; the first absorption membrane A09 is in a stationary state or a rotating state after the high-energy analysis subsystem is started.

(28) As shown in FIG. 2, an output end of the high-current accelerator subsystem 22 is connected with an input end of the first magnetic analyzer A03; between an output end of the first magnetic analyzer A03 and the electrostatic analyzer A05 has the first absorption membrane A04; an output end of the electrostatic analyzer A05 is connected with an input end of the second magnetic analyzer A06.

(29) In which, the first magnetic analyzer A03 is configured for eliminating the isotopic background with the same charge state. For instance, when measuring 10Be.sup.3+, there is an interference with stable isotope .sup.9Be.sup.3+ etc., thus the first magnetic analyzer A03 is configured for eliminating .sup.9Be.sup.3+. The first absorption membrane A04 is configured for eliminating the interference with the isobars. When measuring .sup.10Be.sup.3+, there is an strong interference with .sup.10B.sup.3+, thus the first absorption membrane A04 can eliminate .sup.10B.sup.3+. Since the absorption of the membrane is related to the atomic number of incident ions, when both .sup.10Be.sup.3+ and .sup.10B.sup.3+ pass through this absorption membrane A04, the energy therebetween would be different. The electrostatic analyzer A05 and the second magnetic analyzer A06 may select .sup.10Be.sup.3+ and eliminate .sup.10B.sup.3+.

(30) In which, a Faraday cup is also provided at the output end of the first magnetic analyzer A03, which is used to measure the isotope which is not in the high-resolution detector subsystem 24.

(31) In some embodiments, the first absorption membrane (Si3N4) A04 can stand still, which is similar with the traditional AMS.

(32) Preferably, the first absorption membrane (Si3N4) can be rotated, by rotating the first absorption film, the thickness of high-energy particles passing through the absorption film can be changed, which is more conducive to the elimination of isobaric background.

(33) Preferably, in another embodiment, with reference to FIG. 2, the high-resolution detector subsystem 24 includes a second absorption membrane A07 and a high-resolution detector A08 which are connected in sequence; the second absorption membrane A07 is in a stationary state or in a rotating state after the high-resolution detector subsystem 24 is activated.

(34) With reference to FIG. 2, between an output end of the second magnetic analyzer A06 and the high-resolution detector A08 has a second absorption membrane A07.

(35) In practice, the second absorption membrane A07 is disposed before the window of the high-resolution detector A08.

(36) In practice, the second absorption membrane (SiN) A07 may stand still, which is similar to the traditional AMS.

(37) Preferably, the second absorption membrane A07 may be rotated, rotating the second absorption membrane A07 may change thickness of the high-energy ions passing through the absorption membrane, which is more convenient to eliminate the isobaric background.

(38) Since the high-energy analysis subsystem 23 cannot completely eliminate the interference of the isobars, for example, when measuring .sup.10Be.sup.3+, there would still be a certain amount of .sup.10B.sup.3+, and the second absorption membrane A07 is used to make the energy difference between .sup.10Be.sup.3+ and .sup.10B.sup.3+ again. In this way, the high-resolution detector A08 may be used to eliminate .sup.10B.sup.3+ while recording .sup.10Be.sup.3+.

(39) Preferably, the high-resolution detector subsystem is a 4ΔE gas detector.

(40) Understandable, 4ΔE represents a gas detector with two cathodes and two anodes. The energy resolution of the 4ΔE gas detector is significantly improved, and combined with the energy difference produced by the second absorption membrane A07, the detector subsystem 24 has a greatly enhanced ability to eliminate isobaric background. The 4ΔE gas detector can be understood as a gas ionization chamber.

(41) Of course, according to embodiments of the present disclosure, a gas detector with more cathodes and more anodes can be used, no limitation thereto in the present application.

(42) Preferably, the system further includes a control subsystem that is respectively connected with the ECR high-current positive ion source subsystem, the injector subsystem, the high-current accelerator subsystem, the high-energy analysis subsystem and the high-resolution detector subsystem to control operation of all subsystems.

(43) In this embodiment, the control subsystem may be set up by a computer system, in which the computer system sends requests to control subsystems.

(44) In the AMS technical field, taking into account two things: first, the tandem accelerator has good unity and high energy, which is beneficial for eliminating background; second, the negative ion source has a capability of eliminating isobaric background. The isobars of some radionuclide cannot form negative ions, for instance, the isobar .sup.14N cannot form negative ions when measuring .sup.14C; the isobar .sup.26Mg cannot form negative ions when measuring .sup.26Al. Therefor, since the AMS started to show up, sputtering negative ion source has been used. However, along with developing of geological, environmental, archaeology and marine sciences, the isotope abundance ratio of radionuclides to be measured ranges from 10.sup.−12 to 10.sup.−17, the current AMS apparatus cannot satisfy the need for the abundance sensitivity.

(45) In the present disclosure, the inventors disclose an AMS measuring system based on the ECR ion sources, the method of the ECR high-current positive ion source subsystem extracting positive ions of multi-charge states is firstly introduced in AMS technical field, the method has the following advantages:

(46) Higher ion power is gained by the ECR high-current positive ion source subsystem extracting positive ions of multi-charge states, when there is higher ion powers, it is more beneficial to eliminate background while provide abundance sensitivity. For instance, if the accelerating voltage of the accelerator is 600 kV, when extracting ions of 1+ charge state, the ion powers of the 10Be.sup.1+ and 10B.sup.1+ are both 600 KV; when extracting ions of 2+ charge state, the ion powers of the 10Be.sup.1+ and 10B.sup.2+ are both 1200 KV, of which the ion energy has positive correlation with the charge state. And the improvement of the ion energy has a positive correlation with how much to eliminate 10B.

(47) The embodiment of the present disclosure has following advantages:

(48) Firstly, high-strength beam intensity, since the ECR high-current positive ion source subsystem may produce ions of multi-charge states such as +2, +3, +4, . . . , etc., the beam intensity thereof may range from 10 μA to 100 mA, which is more than 100 times compared with the beam intensity obtained by the traditional AMS to sputter negative ion sources.

(49) Secondly, high efficiency, the producing efficiency of ion sources and conveying efficiency of the system can reach 1% to 10%, the overall efficiency thereof is higher than 10 to 1000 times compared with traditional AMS.

(50) Thirdly, high-energy, the energy of accelerated ions is proportional to the charge state, only more than +2 charge state are selected, the overall energy may be higher than the energy of the ions generated by traditional AMS (usually less than 1 MV).

(51) Fourthly, high charge state without molecular ion background, the ECR high-current positive ion source subsystem generates multi-charge states without generating molecular ions.

(52) Fifthly, the ability to depress 10B with the 2+ charge state is stronger. 2+10B has low ionization degree and high energy to depress the 10B.

(53) Sixthly, the detecting line is lower, which ranges from 10 to 100 atoms. The detection line of traditional AMS ranges from 100 to 10000 atoms.

(54) Seventhly, inert gas such as .sup.39Ar, .sup.85Kr and .sup.133Xe etc. is available for AMS measuring.

(55) In conclusion, due to the aforementioned advantages, the AMS system of the present disclosure is high in beam, high in overall efficiency and strong in how-down capability, and can greatly improve the abundance sensitivity of measurement. The isotope abundance ratio can reach a range from 10.sup.−16 to 10.sup.−18, which is higher than 10 to 1000 times compared with the traditional AMS.

Second Embodiment

(56) With reference to FIG. 3, which shows a flow chart of an accelerator mass spectrometry measuring method according to the embodiment of the present disclosure, the method includes:

(57) Step 310, generating high-current positive ions of multi-charge states by the ECR high-current positive ion source subsystem.

(58) As described in embodiment one, the ECR high-current positive ion source subsystem may be used to detect objects that need to be measured, generating positive ions of multi-charge states, such as Be.sup.2+ or, Be.sup.3+ etc.

(59) Of course, in some embodiments, the subsystem can measure .sup.10Be and .sup.14C, and also measure for .sup.3H, .sup.26Al, .sup.32Si, .sup.36Cl, .sup.41Ca, .sup.129I, U and Pu, isotope and super actinide, and other nuclide measurement, more especially realize highly sensitive measurement of other inert gases such as .sup.85Kr and .sup.133Xe.

(60) Step 320, injecting the high-current positive ions into a high-current accelerator subsystem by an injector subsystem;

(61) After high-current positive ion beams generated by the ECR high-current positive ion source subsystem is outputted to the injector subsystem, the former accelerating section A01 is used to accelerate the beams beforehand, after the ions pass through the low-energy end magnetic analyzer A02, a good mass resolution can be obtained. The low-energy end magnetic analyzer A02 is used to select the mass-to-charge ratio of the ion to be accelerated, where the mass-to-charge ratio is the ratio of the mass number to the charge state. For example, if .sup.9Be.sup.3+ is selected for acceleration, its mass-to-charge ratio is 9/3.

(62) Step 330, accelerating the high-current positive ions by the high-current accelerator subsystem with an accelerating voltage corresponding to the high-current positive ions.

(63) The accelerating voltage of the high-current accelerator subsystem 22 ranges from 0˜800 kV. The subsystem 22 can directly accelerate the ion beams selected by the low-energy end magnetic analyzer A02 without the stripper, thus no need to perform stripping operation on the ion beams.

(64) Step 340, carrying out high-energy analysis on ion beams outputted from the high-current accelerator subsystem by a high-energy analysis subsystem.

(65) According to embodiments of the present disclosure, the high-energy analysis subsystem 23 includes: a first magnetic analyzer A03, a first absorption membrane A04, an electrostatic analyzer A05 and a second magnetic analyzer A06. The first absorption membrane A04 is configured for eliminating the interference with the isobars. When measuring .sup.10Be.sup.3+, there is an strong interference with .sup.10B.sup.3+, thus the first absorption membrane A04 can eliminate .sup.10B.sup.3+. Since the absorption of the membrane is related to the atomic number of incident ions, when both .sup.10Be.sup.3+ and .sup.10B.sup.3+ pass through this absorption membrane A04, the energy therebetween would be different. The electrostatic analyzer A05 and the second magnetic analyzer A06 may select .sup.10Be.sup.3+ and eliminate .sup.10B.sup.3+ based on the differential between .sup.10Be.sup.3+ and .sup.10B.sup.3+.

(66) Of course, according to embodiments of the present disclosure, the thickness of high-energy particles passing through the absorption film can be changed, which is more conducive to the elimination of isobaric background.

(67) Step 350, detecting positive ions after high-energy analysis performed by a high-resolution detector subsystem.

(68) As mentioned above, the high-resolution detector subsystem 24 includes a second absorption membrane A07 and a high-resolution detector A08. Because the high-energy analyzer subsystem 23 cannot completely eliminate the interference of the isobars, for example, when measuring .sup.10Be.sup.3+, there would still be a certain amount of .sup.10B.sup.3+, and the second absorption membrane A07 is used to make the energy difference between .sup.10Be.sup.+ and .sup.10B.sup.3+ again. In this case, the high-resolution detector A08 may be used to eliminate .sup.10B.sup.3+ while recording .sup.10Be.sup.3+.

(69) Of course, in embodiments of the present disclosure, by rotating the second absorption membrane A07 may change thickness of the high-energy ions passing through the absorption membrane, which is more convenient to eliminate the isobaric background.

(70) The embodiment of the present disclosure has following advantages:

(71) 1. high-strength beam intensity; 2. high-efficiency; 3. high-energy; 4. high-charge state without molecular ion background; 5. simple structure and easy to be miniaturized; 6. available for AMS measurement on inert gas; 7. strong capability of using 2+ charge state to depress 10B; 2+10B has a low ionization degree, and high-energy to depress 10B; 8. the detecting line is lower, which ranges from 10 to 100 atoms, whereas, the detection line of traditional AMS ranges from 100 to 10000 atoms.

(72) In conclusion, due to the aforementioned advantages, the AMS system of the present disclosure is high in beam, high in overall efficiency and strong in how-down capability, and can greatly improve the abundance sensitivity of measurement. The isotope abundance ratio can reach a range from 10.sup.−16 to 10.sup.−18, which is higher than 10 to 1000 times compared with traditional AMS.

(73) Further, the description for the second embodiment about the measuring method is comparatively simple since the second embodiment is similar with the aforementioned device embodiment.

(74) Further, the description between every embodiment is laid out progressively, the differentials between every embodiment are illustrated purposely, the similarity between every embodiment can be referred each other.