RussianPatents.com

Time-of-flight mass spectrometre

Time-of-flight mass spectrometre
IPC classes for russian patent Time-of-flight mass spectrometre (RU 2381591):

H01J49/40 - Time-of-flight spectrometers (H01J0049360000 takes precedence);;
Another patents in same IPC classes:
Mass-sensitive selective concentrator for ion mobility spectroscopy (ims) Mass-sensitive selective concentrator for ion mobility spectroscopy (ims) / 2379678
Invention relates to analytical instruments, particularly, to devices intended for preliminary concentration of analyzed sample and combined with analytical instrument that can be used to produce fast-operation analyzers of poisonous or explosive substance concentration in air. Proposed concentrator comprises analyzed sample fast-desorption absorbing element and acoustic transducer with its output signal depending upon mass of absorbed sample. Acoustic transducer represents a piezoelectric plate-sound conductor with two built-in interdigital electromechanical transducers (IDT), designed to excite and receive surface acoustic waves (SAW). While absorbing element represents a film made from molecular imprinting polymer applied onto said plate-sound receiver surface and consisting of two sections, i.e. small-area detecting section located on SAW propagation line, and larger-area concentrating section located outside acoustic line. Said concentrating section can comprise two additional sections to double as SAW-absorbing coatings. To this end, said additional sections are arranged on plate-sound receiver surface, on SAW propagation line outside the space between IDT.
Mass spectrometer for macromolecule analysis Mass spectrometer for macromolecule analysis / 2332748
Mass spectrometer contains holder with analysed substance, ionisator and supplier of macromolecules to mass analyser, and detector. Mass analyser is connected to holder with analysed substance, and detector is based on matrix of micromechanical cantilevers providing determination of interaction time point and point where accelerated macromolecule contacts with petal surface of micromechanical cantilever, providing macromolecule pulse transfer to micromechanical cantilever petal, and following deviation of petal by the distance determined by weight and energy of macromolecule. Thus detector is implemented within consistently optically connected emitting sources, collimating optics, micromechanical cantilever matrix, projecting optics and photodetector, while micromechanical cantilever matrix thereof is designed as detector substrate where micromechanical cantilevers are mounted, thus micromechanical cantilever is designed as part of leg, arm, reflecting layer. Micromechanical cantilever matrix is multielement.
Method and device for identification of organic compounds Method and device for identification of organic compounds / 2329563
Invention is related to the field of gas analysis, in particular of vapours of explosive, narcotic and poisoning substances. Method of organic compounds identification consists in measurement of volt-ampere characteristics with application of surface-ionisation source of ions, in which measurement of volt-ampere dependence is carried out in interval of voltages "thermal emitter of ions - electrode for ion current control" from U1 to U4, volt-ampere dependence section is separated from U2 to U3>U1, in which value of current of organic compounds ions quadratically depends on value of voltage "thermal emitter of ions - electrode for ion current control", at that U1 and U4 are selected based on conditions U4>U3, U1<U2, at that volt-ampere dependence is used for determination of value of organic compounds ions drift mobility and/or for determination of energy activation value of organic compounds molecules ionisation on thermal emitter surface, at that for determination of organic compounds ions drift mobility value section is used from U2 to U3 of volt-ampere characteristic, and for determination of energy activation value of organic compounds molecules ionisation section is used from U3 to U4 of volt-ampere characteristic. Device is suggested for identification of organic compounds, which contains two structurally identical surface-ionisation sources of organic compounds ions, at that inlet openings of channels of nozzles for intake of analysed air flows of the first and second sources of ions are combined into common channel of common nozzle for intake of analysed air flow.
Ion mobility spectrometer Ion mobility spectrometer / 2328791
Ion mobility spectrometer contains the neoformation chamber with installed ion source, drift chamber with the ion collector and aperture mesh, ejecting electrode and the mesh gate which form the ejection area, holes for supplying the mixture of the analised substance with carrier gas, and drifting gas and for outputting the drift gas and the mixture of the analised substance with carrier gas. The chamber of ion-formation with the ion source is placed out of the ejection area and connected with it via adapter with the canal for ion transportation; at that, the ion-formation chamber has the potential of the mesh gate. The adaptor canal has the conical shape, at the ion-formation chamber, which becomes slit-like at the ejection area. The planes of the slit-like canal are parallel to the mesh gate. The length of the slit-like canal is selected so as to guide the ion and carrier gas flow along the ejecting electrode and the mesh gate. The length of the slit-like canal is more or equal to the canal's width, and the canal's width is equal to or less than the distance between the mesh gate and the ejecting electrode.
Mass selective device and analysis method for drift time of ions Mass selective device and analysis method for drift time of ions / 2327245
Invention pertains to the field of dynamic mass analysis of charged particles in alternating HF fields. The mass-selective method of separating ions is based on the use of an analyser, consisting of two flat parallel electrodes with linear-discrete and anti-phased HF potential distributions on the Y axis and a flat earthed electrode, and a limiting electrode with values y≥0. The discrete electrodes are made in the form of capacitor or inductive linear HF voltage dividers. Applied to the electrodes are two anti-phased HF voltages with constant amplitude Um and frequency, ω for which a linear alternating electrical field is formed in the analyser on the X and Y axis. Ions are put into the analyser through the opening in the flat earthed electrode with initial coordinates xn>0, уn=0 and initial velocities vu, inversely proportional to the masses, m of the analysed ions. Ions on the X and Y axes have almost harmonic oscillations with the same amplitude уm and period T, proportional to mass m. During the analysis period the x coordinate of the ions changes to the opposite x(tA)=-xn, while the y coordinate becomes equal to y(tA)=0. The sorted out ions in accordance of their mass m, successively pass into the analyser and reach the registration system.
Dust impact mass spectrometer Dust impact mass spectrometer / 2326465
Invention relates to the instrument engineering, automation means, and control systems, namely, to the space research area. The dust impact mass spectrometer contains a hemispheric target with one opening in the middle of its surface, which increases the probability of target impact with a micrometeorite at the same dimensions of the mass spectrometer. The accelerating gap is a limited by a hemispheric target and a hemispheric grid, located concentrically, which provides equal ion trajectory lengths, thus eliminating the measurement result dependence on the impact location and increases the measurement result reliability. The parabolic reflector focuses ions into a parallel beam directed exactly to the hemispheric target opening.
Transit-time method for metering charge and mass composition of plasma ions Transit-time method for metering charge and mass composition of plasma ions / 2314594
Proposed method involves immersion of drift tube into plasma followed by acceleration of ions by applying negative-polarity voltage pulse across drift tube, pulse length being shorter than its transit time within drift tube carrying analyzed plasma accelerated ions at highest Z/Mi ratio, where Z is degree of ion charge in plasma; Mi is ion mass; this is followed by separating ions with respect to their mass, charge, and energy as they are conveyed through equipotential space of drift tube, as well as measurement of ion current pulse at drift tube outlet; then second measurement similar to first one is made but for different length of negative-polarity voltage pulse supplied to drift tube; charge and mass composition of plasma ions is evaluated by subtracting results of measuring ion current pulses at outlet of drift tube obtained at different lengths of negative-polarity voltage pulses.
Transit-time mass spectrometer Transit-time mass spectrometer / 2295797
Proposed mass spectrometer that can be used for solving problems in organic chemistry, biochemistry, immunology, medicine, biotechnology, environment control, for evaluating composition and properties of materials in industry and scientific research has pulsed ion source, drift space with two flat braking-field wire-net capacitors and detector installed in tandem at its end is provided with second drift space formed by common electrodes of flat wire-net capacitors spaced along device axis; potential of second drift space is braking one with respect to first drift space.
Analyzer of energies of charged particles Analyzer of energies of charged particles / 2294579
Analyzer of charged particles energy contains sample (emitting charged particles), external electrode and internal electrode with two circular slits and detecting system. Axial and radial gradients of energy analyzer field potential are synchronized along movement route of charged particles by setting appropriate configuration of equipotential surfaces of analyzer electrodes.
Ion spectrum measurement process and transit-time ion spectrometer Ion spectrum measurement process and transit-time ion spectrometer / 2266587
Charge and mass composition is measured by accelerating ions in accelerating gap formed in vacuum chamber between input end of drift tube and plasma when negative-polarity voltage pulse of length shorter than transit time in drift tube of accelerated ions of plasma being analyzed is applied to drift tube at maximal Z/Mi ratio, where Z is ion charge in plasma; Mi is ion mass. Voltage pulse is supplied from negative-polarity accelerating-voltage pulse source whose high-voltage lead is electrically connected to drift tube and other lead, to vacuum-chamber ground. When in transit, accelerated ions are divided within drift tube into mass, charge, and energy clots and separated clots are recorded by detector.
Ion spectrum measurement process and transit-time ion spectrometer Ion spectrum measurement process and transit-time ion spectrometer / 2266587
Charge and mass composition is measured by accelerating ions in accelerating gap formed in vacuum chamber between input end of drift tube and plasma when negative-polarity voltage pulse of length shorter than transit time in drift tube of accelerated ions of plasma being analyzed is applied to drift tube at maximal Z/Mi ratio, where Z is ion charge in plasma; Mi is ion mass. Voltage pulse is supplied from negative-polarity accelerating-voltage pulse source whose high-voltage lead is electrically connected to drift tube and other lead, to vacuum-chamber ground. When in transit, accelerated ions are divided within drift tube into mass, charge, and energy clots and separated clots are recorded by detector.
Analyzer of energies of charged particles Analyzer of energies of charged particles / 2294579
Analyzer of charged particles energy contains sample (emitting charged particles), external electrode and internal electrode with two circular slits and detecting system. Axial and radial gradients of energy analyzer field potential are synchronized along movement route of charged particles by setting appropriate configuration of equipotential surfaces of analyzer electrodes.
Transit-time mass spectrometer Transit-time mass spectrometer / 2295797
Proposed mass spectrometer that can be used for solving problems in organic chemistry, biochemistry, immunology, medicine, biotechnology, environment control, for evaluating composition and properties of materials in industry and scientific research has pulsed ion source, drift space with two flat braking-field wire-net capacitors and detector installed in tandem at its end is provided with second drift space formed by common electrodes of flat wire-net capacitors spaced along device axis; potential of second drift space is braking one with respect to first drift space.
Transit-time method for metering charge and mass composition of plasma ions Transit-time method for metering charge and mass composition of plasma ions / 2314594
Proposed method involves immersion of drift tube into plasma followed by acceleration of ions by applying negative-polarity voltage pulse across drift tube, pulse length being shorter than its transit time within drift tube carrying analyzed plasma accelerated ions at highest Z/Mi ratio, where Z is degree of ion charge in plasma; Mi is ion mass; this is followed by separating ions with respect to their mass, charge, and energy as they are conveyed through equipotential space of drift tube, as well as measurement of ion current pulse at drift tube outlet; then second measurement similar to first one is made but for different length of negative-polarity voltage pulse supplied to drift tube; charge and mass composition of plasma ions is evaluated by subtracting results of measuring ion current pulses at outlet of drift tube obtained at different lengths of negative-polarity voltage pulses.
Dust impact mass spectrometer Dust impact mass spectrometer / 2326465
Invention relates to the instrument engineering, automation means, and control systems, namely, to the space research area. The dust impact mass spectrometer contains a hemispheric target with one opening in the middle of its surface, which increases the probability of target impact with a micrometeorite at the same dimensions of the mass spectrometer. The accelerating gap is a limited by a hemispheric target and a hemispheric grid, located concentrically, which provides equal ion trajectory lengths, thus eliminating the measurement result dependence on the impact location and increases the measurement result reliability. The parabolic reflector focuses ions into a parallel beam directed exactly to the hemispheric target opening.
Mass selective device and analysis method for drift time of ions Mass selective device and analysis method for drift time of ions / 2327245
Invention pertains to the field of dynamic mass analysis of charged particles in alternating HF fields. The mass-selective method of separating ions is based on the use of an analyser, consisting of two flat parallel electrodes with linear-discrete and anti-phased HF potential distributions on the Y axis and a flat earthed electrode, and a limiting electrode with values y≥0. The discrete electrodes are made in the form of capacitor or inductive linear HF voltage dividers. Applied to the electrodes are two anti-phased HF voltages with constant amplitude Um and frequency, ω for which a linear alternating electrical field is formed in the analyser on the X and Y axis. Ions are put into the analyser through the opening in the flat earthed electrode with initial coordinates xn>0, уn=0 and initial velocities vu, inversely proportional to the masses, m of the analysed ions. Ions on the X and Y axes have almost harmonic oscillations with the same amplitude уm and period T, proportional to mass m. During the analysis period the x coordinate of the ions changes to the opposite x(tA)=-xn, while the y coordinate becomes equal to y(tA)=0. The sorted out ions in accordance of their mass m, successively pass into the analyser and reach the registration system.
Ion mobility spectrometer Ion mobility spectrometer / 2328791
Ion mobility spectrometer contains the neoformation chamber with installed ion source, drift chamber with the ion collector and aperture mesh, ejecting electrode and the mesh gate which form the ejection area, holes for supplying the mixture of the analised substance with carrier gas, and drifting gas and for outputting the drift gas and the mixture of the analised substance with carrier gas. The chamber of ion-formation with the ion source is placed out of the ejection area and connected with it via adapter with the canal for ion transportation; at that, the ion-formation chamber has the potential of the mesh gate. The adaptor canal has the conical shape, at the ion-formation chamber, which becomes slit-like at the ejection area. The planes of the slit-like canal are parallel to the mesh gate. The length of the slit-like canal is selected so as to guide the ion and carrier gas flow along the ejecting electrode and the mesh gate. The length of the slit-like canal is more or equal to the canal's width, and the canal's width is equal to or less than the distance between the mesh gate and the ejecting electrode.
Method and device for identification of organic compounds Method and device for identification of organic compounds / 2329563
Invention is related to the field of gas analysis, in particular of vapours of explosive, narcotic and poisoning substances. Method of organic compounds identification consists in measurement of volt-ampere characteristics with application of surface-ionisation source of ions, in which measurement of volt-ampere dependence is carried out in interval of voltages "thermal emitter of ions - electrode for ion current control" from U1 to U4, volt-ampere dependence section is separated from U2 to U3>U1, in which value of current of organic compounds ions quadratically depends on value of voltage "thermal emitter of ions - electrode for ion current control", at that U1 and U4 are selected based on conditions U4>U3, U1<U2, at that volt-ampere dependence is used for determination of value of organic compounds ions drift mobility and/or for determination of energy activation value of organic compounds molecules ionisation on thermal emitter surface, at that for determination of organic compounds ions drift mobility value section is used from U2 to U3 of volt-ampere characteristic, and for determination of energy activation value of organic compounds molecules ionisation section is used from U3 to U4 of volt-ampere characteristic. Device is suggested for identification of organic compounds, which contains two structurally identical surface-ionisation sources of organic compounds ions, at that inlet openings of channels of nozzles for intake of analysed air flows of the first and second sources of ions are combined into common channel of common nozzle for intake of analysed air flow.
Mass spectrometer for macromolecule analysis Mass spectrometer for macromolecule analysis / 2332748
Mass spectrometer contains holder with analysed substance, ionisator and supplier of macromolecules to mass analyser, and detector. Mass analyser is connected to holder with analysed substance, and detector is based on matrix of micromechanical cantilevers providing determination of interaction time point and point where accelerated macromolecule contacts with petal surface of micromechanical cantilever, providing macromolecule pulse transfer to micromechanical cantilever petal, and following deviation of petal by the distance determined by weight and energy of macromolecule. Thus detector is implemented within consistently optically connected emitting sources, collimating optics, micromechanical cantilever matrix, projecting optics and photodetector, while micromechanical cantilever matrix thereof is designed as detector substrate where micromechanical cantilevers are mounted, thus micromechanical cantilever is designed as part of leg, arm, reflecting layer. Micromechanical cantilever matrix is multielement.
Mass-sensitive selective concentrator for ion mobility spectroscopy (ims) Mass-sensitive selective concentrator for ion mobility spectroscopy (ims) / 2379678
Invention relates to analytical instruments, particularly, to devices intended for preliminary concentration of analyzed sample and combined with analytical instrument that can be used to produce fast-operation analyzers of poisonous or explosive substance concentration in air. Proposed concentrator comprises analyzed sample fast-desorption absorbing element and acoustic transducer with its output signal depending upon mass of absorbed sample. Acoustic transducer represents a piezoelectric plate-sound conductor with two built-in interdigital electromechanical transducers (IDT), designed to excite and receive surface acoustic waves (SAW). While absorbing element represents a film made from molecular imprinting polymer applied onto said plate-sound receiver surface and consisting of two sections, i.e. small-area detecting section located on SAW propagation line, and larger-area concentrating section located outside acoustic line. Said concentrating section can comprise two additional sections to double as SAW-absorbing coatings. To this end, said additional sections are arranged on plate-sound receiver surface, on SAW propagation line outside the space between IDT.

FIELD: physics.

SUBSTANCE: proposed invention relates to mass spectrometry with orthogonal entry of ions and is widely used in organic and bioorganic chemistry, immunology, biotechnology and medicine when ionising analysed substances using an electron impact method, electrospray etc. The time-of-flight mass spectrometre consists of an electrospray type ion source, an orthogonal ion accelerator (pulser), which includes regions for accumulation and acceleration of ions, field-free drift space, two-stage mirror and detector. The accumulation region of the pulser is made in form of a monopole whose grounded electrode edge is combined with the grounded grid of the acceleration region. There is an ion exit slit in the grounded electrode edge of the monopole.

EFFECT: increased resolution of the time-of-flight mass spectrometre.

2 cl, 3 dwg

 

The present invention relates to the field of mass spectrometry with orthogonal input ions and will find wide application in solving problems in organic and Bioorganic chemistry, immunology, biotechnology and medicine during ionization of the compounds under investigation by electron impact, "electrospray" and others. At the existing time-of-flight mass spectrometers with orthogonal input ions there are several factors limiting the resolution of the device, two of which are essential for time-of-flight mass spectrometer with orthogonal input, the first due to the width of the ion beam in the area of accumulation, and the other by the range of ion velocities at the moment of start. In other words, the decisive factor limiting resolution time-of-flight instruments, is the presence of non-zero phase volume (φ=ΔvΔx) of the ion beam in the area of accumulation of the orthogonal accelerator (PALSAR).

Orthogonal to the velocity dispersion of the ions in the field of accumulation Pulsera leads to time reversal (turn around time), which cannot be compensated by any analyzers, containing only homogeneous field and bespravie intervals. Therefore, time reversal is the main factor limiting resolution time-of-flight instrument with orthogonal input ion PU is CA.

Known time-of-flight mass spectrometer [1], consisting of a pulsed ion source, bespolovogo drift space, a two-stage electrostatic mirror and the detector, which is good enough (to second order) is compensated by the variation of the initial energies of the ions of the same type. However, it is not possible to obtain a higher degree of ion focusing on energy, and consequently, to achieve a significant increase resolution without significantly increasing the dimensions of the device.

Also known time-of-flight mass spectrometer [2], consisting of a pulsed ion source, bespolovogo drift space, two flat net capacitors inhibitory fields separated by the second bespaleva interval, and the ion detector. This mass spectrometer is achieved by focusing the third order energy, however, and its resolution is significantly limited uncompensated effect of time reversal ions in the orthogonal input method.

The closest of the known devices is time-of-flight mass spectrometer MX 5303 [3] with orthogonal input ion beam, selected as a prototype. It consists of an ion source for producing ions of Bioorganic substances used method of extraction of ions from solutions at atmospheric pressure (electrospray"); system of differential pumping with a cooling gas transport and focusing quadrupole systems; orthogonal accelerator (pulser) with a uniform electrostatic field in the area of accumulation of ions (from the plate with UPusha grounded grid), and their acceleration (from a grounded grid to the electrode with UAcc); span bespolovogo space, two-stage mirror and the detector. The disadvantage of the prototype is not sufficiently high resolution (R0~ 10000), which is organic, a large time spread of the ions when they are orthogonal acceleration Pulsera with a homogeneous field.

Object of the invention is the reduction of the time-reversal and, consequently, an increased resolution time-of-flight mass spectrometer.

The problem is solved due to the fact that in the known time-of-flight mass spectrometer comprising an ion source of the type "electrospray"orthogonal accelerator (PALSAR), including the area of accumulation and ion acceleration, bespolovogo span space, two-stage mirror and the detector, the area of accumulation Pulsera made in the form of a monopole, the edge of the grounded electrode which is combined structurally combined with the grounded grid area of acceleration.

Offer vremjaproletnyj the th mass spectrometer differs from the prototype in that in the field of accumulation Pulsera using monopole creates an inhomogeneous electrostatic field, which first generates a temporary focus on the field boundary for strictly parallel beam and, secondly, it greatly reduces the time reversal ions for weakly diverging beam that despite a slight increase in the energy spread in the ion package gives the effect of increasing the resolution is approximately two times at a constant geometrical and electrical parameters of the device.

The invention is explained in mathematical calculations and drawings, in which figure 1 is a schematic representation of a mass spectrometer Pulsera with inhomogeneous field figa presents the monopole in the scheme of orthogonal accelerator (PALSAR), figb presents the orthogonal accelerator (PALSAR), creating a uniform electrostatic field - pulser prototype.

Consider the work of the proposed mass spectrometer.

The proposed new device (figure 1) consists of an ion source 1, creating a continuous ion beam, orthogonal accelerator (PALSAR), including the area of accumulation 2 and acceleration 3 ions, bespolovogo drift space 4, the first mirror 5 with a retarding potential, the second mirror 6 having potential, and the ion detector 7.

The proposed device works follow the way.

Continuous ion beam generated in the source 1, falls in the region of accumulation Pulsera 2, where when applying a pulsed potential UPushcreates an inhomogeneous electrostatic field, which cuts out a continuous beam and orthogonal to the original direction accelerates the ion packet, which, falling into the acceleration region with a homogeneous electrostatic field 3, accelerated to an energy of qUAccthat flies in the fieldless span the space of 4; slowing field of the first mirror 5, is reflected in the second mirror 6; accelerated in the field of the first mirror 5, is flying in fieldless space 4 and falls on the detector 7. It is assumed that the velocity vector of the ion package is a small angle with the axis X, as in the prototype.

Let us prove that the proposed device has the effect of reducing the time reversal, bringing with it an increased resolution of the instrument is approximately two times.

In the absence of an electrostatic field of a continuous ion beam is injected along the Z-axis in the region of accumulation Pulsera as close to the rod monopole strictly parallel to the edge of the grounded electrode of the monopole and perpendicular to the X axis pulser. When submitting eject UPushpulse to hyperbolic (or cylindrical) electrode monopole and pull pulse UPullnext after aseminae grid electrode ion package is accelerated first to the ground potential in a two-dimensional field of the monopole, and then to the accelerating potential in a uniform field. Orthogonal accelerated ions enter into the mass analyzer, the parameters of which are identical to the parameters of the prototype.

When submitting eject pulse UPushat the core of the monopole in the field of accumulation palser, i.e. in the space between the electrodes of the monopole, is a two-dimensional field, the potential distribution which is determined by the expression (I):

where UPush- eject the potential on the rod monopole,

anddistance from the rod to the ribs grounded electrode monopole.

The electric field and its components are defined by the relations:

In the field with the potential (1) can be easily integrated the exact equations of motion for ions:

where m, q are the mass and charge of the ion. The solutions of the equations (4) will be:

where x0, y0and V0xV0y- the initial coordinates and the components of the initial velocity of the ion along the axes X and Y, respectively,

For strictly parallel beam, i.e. beam, in which all ions have no tangential component of the velocity (V0x=0), system (5) takes the form:

From the system (6) shows that for any initial coordinates (x0, y0) all ions even from the ribbon beam, and not just a narrow cylindrical, get in the plane of the exit slit of the accumulation area (x=0) at the same time, spending time, defined by the expression (7):

This indicates the presence of intermediate temporary focus on the output of the inhomogeneous field of the proposed device.

Time reversal in an inhomogeneous field, τ is determined from the first equation of system (5).

Putting the arctangent of the expression (8) in a Taylor series, keeping only the first member and given that x0and, we obtain the expression (9)connecting time reversal for heterogeneous τ and uniform τ0fields:

Thus, as (ΔT, ΔT0)<<τ, T≈T0, the resolution R of the proposed mass spectrometer with Pulsera-monopole with respect to time reversal is approximately two times larger than that of the prototype R0, that is, a mass spectrometer with Pulsera with a homogeneous field:

and, thus, the execution of the field of accumulation Pulsera in the form of a monopole contributes to the achievement of the objectives.

Literature

1. Veerathai, Bagamery, Dwick. A new principle focus of IO is different packets in flight mass spectrometers. // ZH - 1971 - v.41, V, s-1501.

2. Ukhalov, Navkrishna, Roublev. // Russian Federation patent No. 2295797. Application for invention No. 2005119734 priority from 16.06.2005 G., "time-of-Flight mass spectrometer.

3. Time-of-flight mass spectrometer with elektrorazpredelenie MX 5303. // Prospectus of the Institute for analytical instrumentation RAS. http://www.iai.rssi.ru

1. Time-of-flight mass spectrometer comprising an ion source of the type "electrospray"orthogonal accelerator (PALSAR), span bespolovogo space, two-stage mirror and the detector, characterized in that the area of accumulation Pulsera made in the form of monopole, creating a quadratic electrostatic field, and the edge of the grounded electrode monopole combined with grounded grid fostering Pulsera with a homogeneous field.

2. Time-of-flight mass spectrometer according to claim 1, characterized in that the edge of the grounded electrode monopole has a slot exit of ions.

 

© 2013-2014 Russian business network RussianPatents.com - Special Russian commercial information project for world wide. Foreign filing in English.