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    • 专利摘要:
    ionic source for direct sample analysis. The present invention relates to a direct sample analysis (dsa) ion source system operating essentially at atmospheric pressure that is configured to facilitate the ionization or desorption and ionization of sample species from a wide variety of gaseous, liquid samples and/or solids for chemical analysis by mass spectrometry or other gas phase ion detectors. The dsa system includes one or more means of ionizing samples and includes a sealed enclosure that provides protection against high voltages and hazardous vapors and in which the former local gaseous environment can be monitored and well controlled. the dsa system is configured to accommodate single or multiple samples at any time and provide external control of individual sample positioning, sample conditioning, sample heating, position detection and temperature measurement.
    公开号:BR112013031106B1
    申请号:R112013031106-1
    申请日:2012-06-01
    公开日:2021-06-22
    发明作者:Craig M. Whitehouse
    申请人:Perkinelmer Health Sciences, Inc；
    IPC主号:
    专利说明:

    Technical Field
    [001] The present invention relates to direct sample analysis systems that include ionic sources that operate at atmospheric pressure and are interfaced to a mass spectrometer or other gas phase detectors. Ion sources can generate ions from multiple samples having widely diverse properties, the samples being introduced directly into the ion sources of the direct sample analysis system. Background
    [002] There has been a rapid growth in recent years in the prevalence and variety of techniques for desorption and ionization of sample species from solid surfaces under ambient atmospheric conditions, without significant sample preparation, followed by chemical analysis by mass spectrometry. Examples of such techniques include, but are not limited to: "electrospray desorption ionization" (DESI); "chemical ionization at atmospheric pressure and by thermal desorption" (TD/APCI); "real-time direct analysis" (DART); "chemical ionization at atmospheric pressure and by desorption" (DAPCI); and "electrospray ionization/laser desorption" (LD/ESI). Recent reviews that enumerate and elucidate such techniques are provided by: Van Berkel GJ, et. al, "Established and emerging atmospheric pressure surface sampling/ionization techniques for mass spectrometry", J. Mass Spectrom. 2008, 43, 1161-1180; and, Venter A., et al, "Ambient desorption ionization mass spectrometry", Trends in Analytical Chemistry, 2008, 27, 284-290.
    [003] Most of such techniques have been demonstrated with ion source configurations that have been open to the environment. Opening configurations is attractive because they can enable easy optimization of analysis conditions such as sample placement and reagent source placement, easy sample handling during analysis such as heating or cooling, and a direct sample changeover. However, the open configuration of the ion source can exhibit serious shortcomings with respect to security concerns that preclude its use in unregulated installations and are inadvisable elsewhere for the same reasons. For example, open source configurations may not provide adequate protection for the operator from accidental exposure to the high voltages and/or high temperatures typically employed in such sources. Open sources may also lack vaporized sample and reagent material which is often very toxic.
    [004] Apart from such safety concerns, ionic sources operating at atmospheric pressure often rely on chemical reactions involving gaseous species that are naturally present in the local environment, such as water vapor, oxygen, and/or nitrogen. As such, the performance of such sources can vary significantly as the local concentration of such reagents drifts uncontrollably, resulting in degrading performance and/or poor reproducibility. There is a significant need for a direct sample analysis system that provides real-time monitoring, response, conditioning and control of sample background and ionization conditions.
    [005] Until now, only a few attempts are known to have been made to configure such an ion source of atmospheric pressure with an enclosure that provides safe operation, and the ability to better control and manipulate the environment. However, such attempts to supply ion sources to the ambient atmosphere with an envelope have, at the same time, compromised some of the most advantageous opening characteristics of ionic sources, such as: the ability to readily optimize the position of samples as well as positions of various desorption and/or ionization components for maximum ionization efficiency and vacuum ion transport during operation; to readily access a sample surface, for example, to monitor surface temperature, or to visualize surface appearance; and the ability to configure mechanisms that allow multiple samples to be loaded into a source at the same time; and, consequently, provide the possibility of automated operation. Accordingly, there has been a need for ambient pressure ion sources that are configured with an enclosure that provides operator protection and environmental control of the environment, while also providing these advantageous characteristics otherwise available with open ambient ion sources.
    [006] Additionally, before the ionic source of the ambient atmosphere was configured to accommodate only a single type of solid, liquid or gaseous samples. Consequently, there is a need for an ambient atmosphere ion source that is capable of accommodating one or more samples of one or more sample types in a relatively compact space, without requiring substantial reconfiguration or operator intervention. Furthermore, there has been a need for ionic sources included in the ambient atmosphere that provide automated identification and automated position optimization, and guidance of samples and auxiliary components such as desorption and/or ionization probes. SUMMARY
    [007] The description refers to modalities of Direct Sample Analysis (DSA) systems that include sample ionization means that operate at atmospheric pressure and enable the direct introduction of a single sample or multiple samples. These samples can vary in homogeneity and states of matter including, but not limited to gas, liquid, solid, emulsions, and mixed phases. The DSA ion source system interfaces with a mass spectrometer or other gas phase detectors, such as an ion mobility analyzer, which analyzes the mass-to-charge or mobility of ions produced in the ion source of the species. sample. The DSA ion source system is configured to generate sample-related ions from samples introduced directly into the housing of the DSA ion source system or near atmospheric pressure. In some embodiments, the ion source includes at least a subset of the following elements: 1. a means for loading and holding single or multiple samples, for example, a set of sample holders having removable grid sample holders, 2. a means for moving and positioning each sample to optimize the analysis of each single or multiple sample, eg a translator set with multiple axes (eg four axes) translator set having one or more linear and rotary degrees of freedom or multiple connections or gear sets, 3. a means to introduce one or more samples of gas, liquid or solid or variable properties automatically, while minimizing the introduction of contamination into the ion source, 4. a means to sense type , size, physical characteristics and position of each sample entered, eg a sensor position, 5. a means to automatically identify types of sample holders, eg for example, laser distance sensors, 6. a means to monitor and eliminate unwanted background or species of contamination, eg an upstream gas flow, a mass spectrometer, 7. a means to heat or condition the surface of the sample before analysis, eg a heating source, 8. a means of heating the sample to dry and/or form samples related to gas phase molecules, eg a light source, 9. a means of sensing the temperature of the surface of the sample, for example, pyrometers and thermocouples, 10. a means to generate reactant ions, electrons, neutral molecules in an excited state (metastable species) or charged droplets to facilitate the ionization of molecules related to the sample, for example, a gloss charge, 11. an angled reagent ion generator that enables the introduction and analysis of multiple samples positioned on a variety of sample holder types and shapes without mechanical or clogging interference. alor, 12. an angled reagent ion generator that includes a rotating output end with interchangeable output channels to maximize sample ionization and ion sampling efficiency, 13. a reagent ion generator that includes multiple gas inlets, a liquid inlet with pneumatic nebulization of the introduced liquid, 14. a means to manually or automatically position the reactant ion, or means for generating electrospray charged droplets to provide optimal performance, for example, positioning sensors used in conjunction with agent assemblies translation, 15. a means for directing sample-related ions generated at atmospheric pressure in a mass spectrometer operating in vacuum for mass analysis for charge, eg, voltages applied to electrodes and optical ions, 16. a casing surrounding the ion source and charged sample holder which isolates the ionization region and the charged sample from the environment outside the enclosure, 17. u A means to automatically control the sample holder, sense, move, purge, ionize and mass spectrometric or ion mobility analysis of ions related to the sample, while the housing of the DSA system is sealed, for example, by control software that includes automated tuning algorithms, 18. other modalities that generate sample-related ions based on one or more methods of electrospray, atmospheric pressure chemical ionization (APCI), photoionization and ionization, and; 19. a moisture sensor to measure the moisture content in the purge gas.
    [008] In some embodiments, the Direct Sample Analysis ionic source simultaneously includes means to introduce one or more gas samples or one or more solid or liquid samples. For example, these means include one or more gas inlets and liquid inlets. Gas samples can be ionized directly in a corona discharge region or through charge exchange with gas phase reagent ions. Solid or liquid samples introduced into the ionic source are evaporated and ionized through charge exchange with corona discharge of generated reactant ions; charge exchange or ionization through collisions with electrospray-generated ions or charged droplets; or with photoionization. Additionally, the sample solution can be introduced directly into the reagent ion generator where the solution is nebulized, vaporized and ionized as it passes through the corona discharge region.
    [009] The means for retaining single or multi-phase solid, liquid or multi-phase samples includes sample holders of different shapes and configurations to accommodate variations in the shape, type, compositions and size of the analyzed sample. The sample holder is positioned in an automatic translation state that moves the sample holder in and through the ion source envelope. In some embodiments, the sample holder translator includes a four-axis motion controller with two axes of rotation and two axes of linear motion. Round rod seals are provided for three axes of motion, providing an efficient, plus low friction seal between the indoor ion source and the environment outside the ion source. A linear motion shaft is completely contained within the ion source housing, eliminating the need for a linear seal from the outside environment. The sample translation agent assembly within the ion source housing includes materials that are chemically inert and do not produce chemical contamination that can contribute to unwanted noise ions or chemical interference in the acquired mass spectrum.
    [0010] In some embodiments, the sample translation agent is configured to enable the loading and unloading of liquid or solid phase samples through a door that is sealed when closed and minimizes the introduction of environmental contamination when open. By sequencing the flow of clean purge gas through the sealed ion source housing, it minimizes the introduction of environmental contamination when loading or unloading sample holders. Purging gas also helps to reduce cross-contamination between sequential samples when generating ions in the sealed housing. When loading or unloading solid and liquid samples, the purge gas is controlled to minimize exposure to the user of volatilized samples within the sealed ion source enclosure. Process clearance of indoor contamination species can be monitored directly using the mass spectrometer or with additional sensors such as a moisture sensor in the purge gas outlet vent. In this way of monitoring, with response depending on the data for the control system, optimal and reproducible conditions for analysis can be carried out after loading samples, drying samples or between sample analyzes to avoid sample to sample propagation.
    [0011] The description includes systems having one or more position sensors to determine zero positions of the sample translation agent, the number of loaded samples, the shape and size of each sample, and the position of each sample surface from the which ions should be generated. Zero position sensors are configured to establish the home or zero position of each translation axis in the sample. In some embodiments, laser distance sensors, eg interferometers, are configured to identify the support type and map the surface contour of the sample supports so that once the samples are loaded, a determination can be made to which the sample positions are filled, the size of each loaded sample and the position of each sample surface. Information provided by the distance sensors is processed by the software and electronic control system to enable optimal placement of each sample for maximum ion generation and mass spectrometer sampling efficiency, avoid collisions between samples with any surface on the housing of the ion source (particularly for large or irregular shaped samples), allocate or move the reagent ion generator to its optimal position, and determine the most efficient sample holder movement sequences for multiple sample analyses.
    [0012] Precise translational control of sample position provides several advantages when using both position sensitivity and ion mobility signal response or by mass spectrometry to respond and optimize. Using both the exact surface position and ion mobility signal response or by mass spectrometry allows the acquisition of more uniform and accurate analytical results particularly for samples having widely variable sizes, surface shapes, topography and properties such as point of Fusion. Optimal ionization and ion collection geometries can be achieved that are independent of sample-to-sample size and surface variations. In addition, inhomogeneous sample surfaces can be positionally manipulated to analyze specific surface features. Surface analysis can be conducted with good spatial resolution by heating the surface with focused light rays or lasers. Surface topography video sensitivity can also be implemented to chemically convey surface features (eg dots on tablets).
    [0013] For many liquid or solid samples, heating is required to vaporize the sample for gas phase ionization. Gas samples may also need heating to prevent sample condensation. Modalities include means for generating heat in a number of different ways, including: distributing heated gas through the reactant ion generator; countercurrent drying gas heating; heating using infrared, white light sources or laser; and direct heating of the sample through the sample holder. Total distributed enthalpy is controlled through heater temperature and gas flow, light or laser intensity, direct heater power, or combinations of multiple heat sources. Enthalpy is a measure of the total energy of a system. In some embodiments, the ion source includes a means for measuring the temperature of samples to provide response temperature control. Such a response improves the uniformity and reproducibility of sample ionization. Examples of means for measuring the temperature of samples include temperature sensors such as thermocouples and pyrometers. Thermocouples provide direct temperature response through gases and samples in contact with thermocouple sensors. Pyrometer sensors configured at the ion source measure temperature of a surface of solid or liquid samples from which evaporating sample molecules are released. Precise temperature measurement and response control enable step-by-step sample conditioning during analysis by applying thermal processes in series including temperature ramps, drying (non-bound water), dehydration (bound water), analyte evaporation, which it is subsequently ionized, and finally, stages of pyrolysis or thermal decomposition that can provide structural information about the sample.
    [0014] The exhibit describes multiple means to generate reactant species to ionize sample molecules through metastable ionization, electron transfer, charge exchange or ion-molecule reactions. Examples of such means include glow discharges. Due to the sealed ion source enclosure during sample analysis, the previous gas composition can be controlled to provide optimal ionization conditions. In particular, the amount of water vapor in the ion source enclosure can be controlled to efficiently generate protonated water while minimizing protonated water clumps. The apparatus characteristic of the description has multiple gas inlets and a liquid inlet with nebulization in the reactant ion generator.
    [0015] Single or multi-phase combinations and species of liquid or gas phases can be introduced and ionized in the heated reactant ion generator. The reactant ion generator heater vaporizes nebulized liquids and some or all of the vapors and gas passing through a corona discharge region positioned near the output end of the reactant ion generator. The corona discharge is positioned within the reagent ion generator, which minimizes distortion of electric fields applied directly to sample ions in the spectrometer and introduced into the reagent ion generator for nebulization, evaporation and ionization through Ionization charge exchange reactions Atmospheric Pressure Chemistry (Atmospheric Pressure Chemical Ionization (APCI)). In some embodiments, the vaporized liquid sample passes directly through the corona discharge region for maximum ionization efficiency.
    [0016] In an example application, water can be completely removed from the ionization region and samples with lower proton affinity than water can be analyzed. Chemical ionization reagents such as methane or ammonia can be introduced to provide higher degrees of selectivity when compared to traditional APCI sources. A wide variety of reagent chemistries can be implemented with this DSA ion source system.
    [0017] In some embodiments, the reagent ion generator, and in some applications the APCI sample ion generator, has an angled geometry. In some embodiments, the axis of the nebulizer and vaporizer is set at an angle to the axis of the output channel generator. The apparatus may include an angled output channel configured to rotate at least 180°, which allows for optimal positioning of the reagent ion generator body and output channel, thereby maximizing analytical performance while minimizing interference from multiple sample holders . The output channel is removable to allow installation of output channel geometries optimized for various sample types. The angled geometry enables optimization of the position and angle of the reagent ion generator output in relation to sample types and in relation to the inlet of the mass spectrometer, while preventing the reagent ion generator body from interfering with the samples and sample holders. The angled geometry also moves the reagent ion generator heater out of the sample holders to prevent pre-heating of samples prior to ionization, thereby minimizing cross-contamination between samples. In some embodiments, the reagent ion generator is positioned entirely within the Direct Analysis Source, which avoids the need for any seals on the enclosure wall except for those seals required for the gas and liquid flow lines. The reagent ion generator includes materials that minimize noise contributions of a chemical nature in the acquired mass spectra.
    [0018] Depending on the sample type and geometry, the reagent ion generator output plane and axis require position adjustment to maximize the efficiency of ionization and ion transport in the mass spectrometer. In some embodiments, the reagent ion generator is mounted to a four-axis translation assembly to enable a wide range of position adjustments within the DSA source housing. The position of the reagent ion generator can be established manually or automatically with feedback from the position sensor to the DSA source control software and electronics. In some embodiments, the position of the reagent ion generator can be automatically established by software and electronics, based on the distance sensor profile of the sample holder type and sample types entered into the ion source housing. Output sections of different diameter and geometry sizes can be swapped in the reagent ion generator to maximize ionization efficiency for different sample types, sizes and species. The reagent ion generator is configured with a replaceable corona discharge needle set. Removal of the angled outlet end facilitates removal and installation of the corona or glow discharge needle assembly.
    [0019] A portion of the sample ions generated by different methods in the ion source chamber is directed to the vacuum inlet port and subsequently into the mass spectrometer where they are mass for analyzed charge. Alternatively, ions generated at the DSA source are directed into a mobile analyzer. In some embodiments of the DSA source, electric fields are applied to one or more electrodes to direct ions through a vacuum orifice against a countercurrent flow of gas. Countercurrent gas flow serves to minimize or prevent unwanted neutral species (particles and molecules) from entering the vacuum, thereby minimizing or eliminating the condensation of neutral species with sample ions in the free jet expansion, and eliminating the contamination of neutral species on the electrode surfaces. Electric fields and electrode geometries are optimized to maximize the sensitivity of the DSA ion source mass spectrometer. The DSA source enclosure minimizes and/or prevents any exposure to high voltage or electrical fields to the user. Mapping sample holder types and sample positions using position sensors to compress the sample holders and the translational agent of the reagent ion generator into the ion source minimizes and/or prevents unwanted contact with electrode surfaces, through samples or by moving the ion source hardware during sample analysis.
    [0020] The description presents the apparatus that includes a sealed housing that reduces and/or prevents ambient contamination of the ion source volume inlet. Such a kind of environment can unpredictably affect the ionization of the sample species or contribute to unwanted interference or chemical noise in the mass spectra. The housing allows for tighter control of the reagent ion species generated in the volume of the ion source, enabling reproducible maximum ionization efficiency and higher ionization specificity for a given sample species.
    [0021] The purge gas flow is configured to sweep the ion source of the sample molecules from the gas phase to reduce the time required between sample analysis and to minimize cross-contamination between samples. Purge gas exits through a vent port where it is exhausted through a safe laboratory vent system. Sealed enclosure with safe gas purge minimizes and/or prevents user exposure to volatilized sample species. In some embodiments, the ion source vent, through which the reagent ion generator gas flows, the countercurrent gas flow, and the purge gas flow outlet are positioned above the sample loading plate in the samples. Gas flow in the DSA source chamber flows through the sample loading plate during sample loading, reducing and/or preventing ambient gas contamination entering the ion source while the sample loading port is open. When the sample loading door is closed, gas flowing over and above the sample loading plate and out of the vent serves to purge the sample loading volume of ambient gas before moving samples into the DSA source volume. This purging process in the sample loading region can also be used to dry the freshly loaded sample if this is desirable for a given sample type. A humidity or humidity sensor positioned in the vent exhaust line or port provides feedback to the control systems and software regarding the degree of drying achieved before moving to the recent loading samples in the DSA source volume. Measuring the degree of drying of each loaded sample provides a way to improve consistency in the moisture remaining (or not remaining) in the sample, which can provide improved consistency across multiple sample analyses.
    [0022] Samples prepared on different days can be conditioned in the DSA system to improve the uniformity of analytical results for the same sample types. For example, the same type of medicinal tablets prepared and run on different days can be dried consistently before analysis to improve the surface uniformity of the sample pill being analyzed.
    [0023] The sealed housing is removable to facilitate cleaning of the ion source. In some embodiments, the housing includes an access door that is sealed when closed. The access door and enclosure have safety sensors that shut off voltages and heaters when the seal on the DSA source enclosure is broken.
    [0024] In some modalities of the DSA source, the translation of the sample holders and the reagent ion generator can be operated in fully automatic mode or with selective manual position adjustment. Sensor position inputs to the software allow the electronics and software control system to establish compressions in the sample holders and in the reagent ion generator translation to avoid hardware collisions or electrical decay in automated or manual translation operation. Ion source control systems are linked to sample lists to provide correlation between generated mass spectrometer data and sample positions on multiple sample holders.
    [0025] Some modalities include software-controlled x-y-z translation capability of the sample and sample point position recording, which enables spatial scanning during mass spectra acquisition. For example, the sample analysis point can trace sample separation lines in layer chromatography traces of sample mixtures. The description also covers the DSA system control software that provides sample-specific ionization method information to the mass spectrometer data evaluation software to optimize the evaluation of acquired data data and report generation. Data dependent response can be applied to the DSA system control software to adjust sample ionization conditions to improve performance.
    [0026] The description presents single or multiple means of ionizing samples. Ionization means include, but are not limited to, reactant ion generation and charged droplets using electrospray, atmospheric pressure chemical ionization, photoionization, corona discharge and glow discharge, employed singly or in combination. Sample ionization means include, but are not limited to, charged droplet absorption and ion generation from charged droplet evaporation, gas phase charge exchange or energy exchange reactions, chemical ionization, photoionization, and laser ionization individually or operating with combinations of ionization types.
    [0027] The DSA system can be used to analyze many states of matter including, but not limited to solids, liquids, gases, emulsions, powders, heterogeneous and multiphase samples and mixtures thereof. DESCRIPTION OF DRAWINGS
    [0028] Figure 1 is a diagram of a modality of a Direct Sample Analysis (DSA) ion source and system that includes a position translatable reagent ion generator and square-shaped sample holders, screen sample targets. multiple orifices and a capillary orifice in a mass spectrometer.
    [0029] Figure 2 is a diagram of an embodiment of gas and liquid introducing means and a reagent ion DSA source generator, and countercurrent drying heater configured with a mesh sample holder.
    [0030] Figure 3 is a cross-sectional view of an embodiment of a reagent ion generator and a vacuum capillary orifice with a source of electrospray charge droplets that includes gas and liquid supplies and interconnections.
    [0031] Figure 4 is a closure of a thin layer chromatography sample target in a DSA system that includes the output of the reagent ion generator configured in a downward angled position, focused light source heating and response of pyrometer temperature.
    [0032] Figure 5 is a closure of a thin layer chromatography sample target in a DSA ion source that includes the output of the reagent ion generator configured in the horizontal position, focused light source heating and temperature response of pyrometer.
    [0033] Figure 6 is a diagram of a DSA ion source system embodiment that includes a multi-axis reactant ion generator position translator with a reactant ion generator output configured in a downwardly angled position , a pyrometer temperature sensor response, a video monitor, and a spring clip sample holder.
    [0034] Figure 7 is a side view of an embodiment of a DSA system that includes a multi-sample mesh target, a light heating source with a response pyrometer, and a reagent ion generation with a translation agent. multiple axes configured with a horizontally positioned output.
    [0035] Figure 8 is a partial cross-sectional view of an embodiment of a DSA system that includes a translation stage of a four-axis sample holder, a multi-axis reagent ion generator translation agent, a sensor of sample position, a light heating source with a response pyrometer and a sample tube holder.
    [0036] Figure 9 is a front view of an embodiment of a DSA ion source system that includes a four-axis multiple sample holder translation agent, loaded with a multiple sample holder, positioned for the analysis of samples of solid tablets.
    [0037] Figure 10 is a cross-sectional view of an embodiment of a four-axis sample holder translator that includes rotatable and layered translational rods having seals.
    [0038] Figure 11 is a front view of a multiple sample holders for pills positioned for sample analysis in a DSA ion source housing with purge gas flow.
    [0039] Figure 12 is a top view of a sample holder positioned for sample analysis in a DSA ion source housing with purge gas flow.
    [0040] Figure 13 is a front view of a multiple sample holders positioned for removal of one embodiment of a DSA ion source housing subsequent to conduction analysis of solid tablet samples loaded with purge gas stream.
    [0041] Figure 14 is a top view of a multi-sample holder positioned for removal of one embodiment of a DSA ion source housing system with purge gas flow.
    [0042] Figure 15 is a front view of a multi-sample holder being removed from one embodiment of a DSA ion source system housing with purge gas flow turned off.
    [0043] Figure 16 is a front view of a multi-sample holder being loaded into one embodiment of a DSA ion source system.
    [0044] Figure 17 is a front view of an embodiment of a DSA ion source system in which the volume involved in the ion source and the volume of the sample loading region are purged after a new sample holder is loaded before conducting sample analysis.
    [0045] Figure 18 is a front view of an embodiment of a DSA ion source system during the steps of target sample identification and sample contour mapping using at least one distance sensor.
    [0046] Figure 19 is a top view of an embodiment of a DSA ion source during the steps of target sample identification and sample contour mapping using at least one distance sensor and sample holder translation.
    [0047] Figure 20 is a front view of an embodiment of a DSA ion source configured with the sample holder positioned for conduit analysis and a reagent ion generator moved to a lower position with its output end automatically rotated 180° to provide optimal distribution of reagent ions for a loaded sample in a vertically positioned tube.
    [0048] Figure 21 is a front view of an embodiment of a DSA ion source that includes electrospray ionization of a solid sample holder formed with a liquid supply to electrospray during analysis.
    [0049] Figure 22 is a mass spectrum of turmeric powder analyzed using a DSA modality and ion source system.
    [0050] Figure 23 shows three mass spectra of three different cooking oils analyzed with one modality of a DSA ion source system.
    [0051] Figure 24 shows positive and negative polarity mass spectra acquired from a Diet Coke sample using one modality of a DSA ion source system.
    [0052] Figure 25 shows three mass spectra acquired from three different types of pepper samples using one modality of a DSA ion source system.
    [0053] As different symbols in the various drawings indicate similar elements. DETAILED DESCRIPTION
    [0054] Open configured ion source for direct analysis of samples are subjected to variations in the composition of the indoor air exposes the end user to the sample being analyzed and any kind of reagent being implemented in the analysis. Gaseous reagent species and volatilized sample material can be inhaled by end users performing the analysis. This exposure can be particularly dangerous when analyzing drugs, newly synthesized compounds, medicinal samples, diseased tissues, toxic materials or even unknown samples such as forensic medicine samples with no available history. When operating open ion sources, changes in interior gas composition can affect ionization efficiency, contribute to interior contamination, add peaks of interfering components to mass spectra, change reactant ion composition and unpredictable temperature, leading to results unpredictable analytics. The description presents devices and methods that enable the analysis of multiple samples introduced directly into an ion source volume involved with precisely monitored and controlled interior gas composition, temperature and flow. Reagent ion generation in a DSA ion source system is tightly controlled and reproducible, increasing the strength and reproducibility of sample analysis. Unlike the open ion source where users are potentially exposed to any voltages applied to electrodes, the DSA ion source system includes the application of electrical fields formed from voltages applied to electrodes configured within the volume of the ion source involved. These applied electric fields direct ions through a hole in vacuum, thereby increasing the analytical sensitivity of the mass spectrometer.
    [0055] Commercially available open ion source typically uses neutral gas flow to pull ion samples generated in a vacuum. This same gas stream also traps unionized contaminant molecules and drags these unwanted species into the vacuum where they can condense on contaminating sample ions or mass spectrometer electrodes in a vacuum. The description presents apparatus and methods that include a countercurrent gas flow to prevent unwanted neutral contamination species from entering the vacuum, while directing sample ions through the hole in the vacuum using focusing electric fields. The DSA ion source system includes a capillary dielectric that allows separation of the input and output ends, both electrically and spatially. This electrical electrode isolation enables different voltages to be applied to the capillary input and output electrodes simultaneously, thereby providing ideal voltages in both the atmospheric pressure ion source and in the vacuum regions, as described in U.S. Patent No. 4,542. 293. Electrostatic focusing of ions at atmospheric pressure enables efficient vacuum sampling of ions against countercurrent drying gas, increasing sensitivity while decreasing unwanted neutral contamination gas or vapor molecules from entering the vacuum.
    [0056] Referring to Figures 1 and 2, a DSA ion source system 1 includes a reagent ion generator set 2, a sample set holder 3 with sample holders 20, 21 and 22 of removable grid, a reagent ion generator translation agent assembly 5, a light heater 7, a pyrometer 8, a video camera 10 with fiber optic and focusing lens input 11, a mass spectrometer capillary input electrode 12, an assembly of nozzle piece electrodes 13, and a housing assembly 14. Sample holder assembly 3 includes three removable sample holders 20, 21 and 22 each with 21 individual sample placement locations as diagrammed. Sample Holder Set 3 supports one to four removable sample holders. Sample holders 20, 21 and 22 include a 24 mesh, typically stainless steel or a porous polymer, onto which a liquid sample is loaded. Mesh 24 is sandwiched between metal plates 25 and 26 for support and assembly. The sample holder assembly 3 is positioned through a four-axis translator set 180 shown in Figures 8, 9, 10 and 11. A translator set 180 includes two linear degrees of two rotary translation movement. which performs a vertical 15, rotary 16, horizontal 17, and horizontal 18 X axis movement of the specimen holder assembly 3.
    [0057] As shown in Fig. 1 and in more detail in Fig. 2, the reactant ion generator 2 includes a liquid inlet 40, a nebulizer gas inlet 41, an auxiliary gas inlet 42, a pneumatic nebulizer 43, a heater 44, a thermocouple 45, a corona discharge needle 48 mounted through an electrical insulator 52 and an angled outlet channel 49. Single component or liquid mixtures distributed through liquid inlet 40 are nebulized in pneumatic nebulizer 43 with gas flowing through the inlet of the nebulizer 41. Nebulized liquid and vehicle gas 54 are evaporated and heated as they pass through the heater 44. The temperature of the gas and vapor mixture exiting the heater 44 is measured using thermocouple 45 which is fed back to the software and control electronics to regulate the heater temperature. Heated gas flows through the angled outlet channel 49 surrounded by the removable end piece 51, and passes through the corona or glow discharge 47. The corona or glow discharge 47 is formed by applying kilovolt potentials of typically positive or negative needle polarity of corona discharge or glow 48 while the output end piece 51 remains at ground or zero volt power. Positive polarity voltage applied to the corona discharge needle or glow 48 produces positive polarity reagent ions. Negative polarity reagent ions are produced by applying negative polarity voltage to the corona discharge needle or glow 48. Heated reagent ions are formed in corona discharge 47. Heated reagent ions and carrier gas pass through the output of the reagent ion generator 50 and move to a sample 27 contained in sample holder grid 24. Alternatively, a glow discharge 47 produces energetic metastable ions or atoms or molecules that interact with reagent gas and the sample to form sample and regent ions.
    [0058] The nebulizer gas inlet 41 is connected to the gas pressure regulator or flow controller 81, which controls the flow rate of the nebulizer gas through the nebulizer 43. The nebulizer gas pressure regulator 81 is connected and controlled through the DSA 82 ion source system electronics and software system. The composition of the nebulizing gas is typically, but not limited to, nitrogen or dry purified air. The liquid inlet 40 is connected to syringe pumps 58 and 59 loaded with syringes 60 and 61 respectively. Syringe pumps 58 and 59 can be processed separately to dispense individual liquid species with controlled flow rate or can be processed simultaneously to generate a flow of mixed liquid composition or form gradients of liquid compositions entering reagent ion generator 2. Alternatively , syringe pumps 58 and 59 can be replaced with any fluid dispensing system known in the art such as a liquid chromatography pump or vials holding pressurized liquid. For many sample types, a desirable positive polarity reagent ion is hydronium or protonated water (H30)+ because hydronium has a very low proton affinity and will readily carry gas phase exchange with any molecule having a higher proton affinity . Protonated water aggregates are less desirable because of the affinity of proton water aggregates with the number of water molecules in the aggregate. Consequently, protonated water aggregates can remove protons from the protonated sample ions in the gas phase, reducing the sensitivity of the sample ion. Due to the closed environment of the DSA source ionization region, the percentage of water in the interior reactant gas can be tightly controlled to maximize hydronium ion production while minimizing protonated water agglomerates.
    [0059] The percentage of water in the gas flowing through the outlet channel 49 is determined by the flow rate of water flowing through the liquid inlet 40, which is nebulized in the pneumatic nebulizer 43, and the total flow of the nebulizer gas and gas auxiliary flowing through gas inlets 41 and 42, respectively. For example, with one liter per minute of nebulizer gas flowing through inlet 41, and syringe pump 58 delivering a flow rate of one microliter per minute to nebulizer 43, after vaporization of the water, which results in approximately 1000x a expansion in volume, the water vapor will have a concentration of approximately 0.1% by volume flowing through outlet channel 49 and corona discharge or glow 47. The percentage of water in this reactant ion gas flow can be accurately adjusted by switching the flow rate delivered by syringe 58 or the flow rates of gas passing through gas inlets 41 and 42. The corona or glow discharge 47 ionizes the nitrogen gas molecules flowing through it, which in turn forms nitrogen ions. hydronium through a series of gas phase reactions known to those skilled in the art. The heated reagent ion gas leaving output channel 49 reagent ion generator at output 50 flows through grid 24, evaporating the sample deposited at sample point 27. The evaporated sample molecules exchange with hydronium ions and form ions of protonated sample, if the sample molecules have a higher proton affinity than passing hydronium ions. Sample ions will be formed in the region 84 downstream of the sample point 27. Sample ions formed then continue to focus on the electric field lines formed by the voltages applied to the nozzle piece electrode 13 and capillary inlet electrode 12 and the sample holder of volt grounded or zero 22. Triggered by the electric field, the sample ions move against the countercurrent gas flow of dry nitrogen 60. The countercurrent gas flow 60 snatches away any neutral water molecule or water clumps and dries water clumps protonated moving with the electric field, thereby reducing and/or preventing neutral water clumps from removing charge from newly formed sample ions, and eliminating neutral sample molecules or water from entering the vacuum. Neutral nitrogen gas and ions enter the vacuum through jet expansion, free from cooling and rapidly formed at the outlet end 85 of capillary orifice 30 in capillary 80 with little or no neutral molecule condensation occurring on the sample ions. The DSA ion source system configured per description provides precise control of reagent ion production and distribution, enabling strong, consistent and reproducible analytical operation. As is desired, the sample itself is a variable being analyzed, because of the reproducible controls and conditions surrounding the sample during operation.
    [0060] Samples with low proton affinity in the case of positive ions can be ionized using reagent ion composition other than water. For example, a sample molecule may not accept a proton from a hydronium ion if it does not have protonation sites, as it may form a coupling with a protonated ammonia ion to form a sample ion with a coupled ammonia ion. Such gas phase reactions are known in the field of Atmospheric Pressure Chemical Ionization (APCI) and Vacuum Chemical Ionization (CI). Ammonia can be distributed in reagent ion generator 2 in liquid form using a 58 or 59 syringe pump as described for water above, or ammonia can be extracted as headspace gas 90 or 91 in vials 87 or 88 respectively. Control of headspace gas flow from vials 87 and 88 is provided by pressure regulator 92 and valve 95. Headspace gas flow from one or both of vials 87 and 88 can be selected by opening or closing valves 96 and 97 respectively. Gas from headspace 90 or 91 flows through connection 99 and inlet 42 on heater 44.
    [0061] Alternatively, different kinds of auxiliary gas flow 98 can be introduced into reagent ion generator 2 via inlet 42. Auxiliary gas flow 98, controlled via gas flow controller 93 and valve 94, can be supplied from a pressurized gas tank. For example, it may be desirable to introduce helium as a reactant gas, because the metastable ionized helium formed in the corona or glow discharge 47 has a high ionization potential, which improves the charge transfer efficiency when this metastable helium or species of ion collide with an atom or molecule of gas phase. Helium is a relatively expensive gas and may not be needed to ionize many sample species. Helium can be mixed with nitrogen or other gases to form a reactant ion mixture. Valves 94, 95, 96 and 97, pressure regulator 92 and gas flow controller 93 are connected to electronic controller 82 or DSA source software to provide software and automated control of some or all of the gas and liquid flows in the reagent ion generator 2. Alternatively, the composition and flow of the auxiliary gas can be controlled manually.
    [0062] As shown in Figures 1 and 2, the syringe pumps or dispensing fluid 58 and 59 and T fluid 83 are positioned outside the sealed housing assembly 14 of the DSA ion source system 1. Similarly, solution vials reagents 87 and 88 with valves following 94 through 97, pressure regulator 92 and flow controller 93 are positioned outside the sealed housing assembly 14, as is the electronics controller module 82. Only inert materials that do not significantly contribute to interior noise of chemistry in the mass spectra, or effect the ionization efficiency of the gas phase sample molecules are configured within the sealed housing assembly 14 of the DSA ion source system 1. Materials configured within the sealed housing assembly 14 are typically , but not limited to metal, ceramic or glass. Fluid or gas fluid channels are connected to the sealed supply through which the housing assembly 14 passes. Wires to the heater 44, thermocouple 45 and electrospray electrodes or needles positioned within the housing assembly 14 are typically electrically insulated with electrical insulators. ceramics. Electrical insulators sealed within the DSA ion source housing assembly 14 may include materials other than ceramic as such materials do not degas to the point where such degassing interferes with sample ionization or to the point where such degassing results in interference spikes or chemical noise in the acquired mass spectra.
    [0063] The reagent ion generator 2 can alternatively be operated as an Atmospheric Pressure Chemical Ionization probe in which a sample is directly ionized. With the sample holder assembly 3 moved from region 84 between the output 50 of the reagent ion generator and the input of the nosepiece 70, the ions generated in corona discharge 47 can be delivered directly to the capillary orifice 30, driven by the fields. electrical equipment as described above. Effectively, reagent ion generator 2 can be operated as a field-free APCI input probe, as described in U.S. Patent Number 7,982,185. For example, a gas sample from a gas chromatograph can be delivered through inlet 40 directly to heater 44 to prevent condensation of the sample component. The carrier gas from gas chromatography is typically helium which provides efficient ionization of the elution gas samples as they pass through the corona or luminescent discharge 47. Alternatively, the gas samples can be introduced into inlet 41 or 42 of the ion generator reagent allowing the introduction of additional reagent ion species in parallel to maximize ionization efficiency. Liquid samples may also be introduced through the inlet 40 of liquid chromatographs, injection valves or other fluid flow systems known to those skilled in the art. For example, the calibration solution, the injected flow from syringe 58 through 40, is nebulized in pneumatic nebulizer 43, vaporized as the nebulized drops pass through heater 44 and ionized as calibration vapor passes through the corona or luminescent discharge 47. Calibration ions directed to mass spectrometer 78 through capillary orifice 30 can be used to adjust and calibrate mass spectrometer 78. Similarly, such calibration ions can also be added during sample 27, or any other sample, ionization can provide internal standard calibration ions for accurate mass measurements in high resolving power mass spectrometers. The mass spectrometer 78 can be, among others, a quadrupole, triple quadrupole, Time of Flight (TOF), Hybrid Quadrupole Time of Flight, Orbitrap, Hybrid Quadrupole Orbitrap, 2D or 3D Ion Trap, Time of Flight mass spectrometer Flight-Time of Flight or Fourier Transformer.
    [0064] Referring to Figures 1 and 2, the countercurrent gas 61 initially passes through the countercurrent gas heater 62, exiting at the outlet of the objective port 70. The countercurrent gas flow rate is controlled through the flow regulator 72 connected to software and electronic controllers 82. Voltages are applied to capillary input electrode 12 and objective holder electrode 13 to direct sample ions into capillary orifice 30, which move against the countercurrent drying gas 60. The carrier gas expanding to the vacuum draws the trapped ions to the vacuum stage 74. Voltages are applied to the capillary exit electrode 76 and the separator electrode 75 to direct the ions exiting capillary port 31 to mass spectrometer 78 to the mass/load analysis.
    [0065] Countercurrent gas flow 60, typically but not limited to nitrogen or dry air, drags out unwanted contaminating neutral molecules, preventing neutral contaminant species from entering the vacuum. Countercurrent gas flow 60 eliminates or minimizes condensation of contamination molecules on sample ions on expansion from the free jet to vacuum and minimizes electrode contamination by unwanted neutral molecule in vacuum. The capillary inlet electrode 12 and the output electrode 76 are spatially and electrically separated.
    [0066] Different voltage values can be simultaneously and independently optimized for the input electrode and the output electrode 13 as described in U.S. Patent No. 4,542,293. For example, the voltage values applied to nosepiece 13, capillary input electrode 12 and capillary output electrode 76 can be set to -300 VDC, -800 VDC and +120 VDC respectively for ion polarity generation positive during DSA ion source operation. An ion-concentrating electric field formed from the voltages applied to the nosepiece electrode 13 and capillary 12 inlet directs sample ions formed near the grounded sample target 27 to capillary orifice 30. The gas flowing through the capillary orifice 30 pushes the ions through the capillary orifice 30 against the decelerating electric field between the capillary inlet and the outlet electrode 12 and 76, respectively. The ions exit capillary orifice 31 at approximately the electrical potential applied to the capillary exit electrode 76 plus the velocity transmitted by the seeded molecular beam. The voltage of the capillary output electrode 76 can be increased relative to the voltage applied to the separator 75 to selectively cause ion fragmentation without changing the electric field in the ionization region of the sample 84. Ion fragmentation may be useful in identifying established compounds or to determine the structure of the compound.
    [0067] Referring to Figure 3, the DSA 1 ion source system can be configured with reagent ion addition sources or charged droplets to increase the ionization efficiency of the sample. The DSA ion source system 1 includes an electrospray needle 103 mounted within housing 14. Liquid delivered from one or more fluid delivery systems or syringe pumps 58 and 59 with syringes 60 and 61 respectively, supplies the reagent liquid. or sample solution through fluid line 107 to electrospray needle 103. The reagent liquid or sample solution is electrosprayed from tip 108 of electrospray needle 103 to form a cloud of charged droplets 104. The electrospray cloud 104 is formed by the difference in voltage applied between the electrospray needle 103 and the nosepiece electrode 13 or the wall 110 of the grounded output channel 49. In some embodiments, the high voltage power supply is connected to the electrospray needle 103 and the voltage adjusted to a value that will sustain a stable electrospray cloud. Alternatively, sufficient voltage can be applied to the nosepiece electrode 13 to provide a stable electrospray with the electrospray needle 103 held at ground potential. Applying voltage to electrospray needle 103 and nosepiece 13 can typically be used to optimize sample ionization efficiency and ion sampling for mass spectrometer 78.
    [0068] Sample molecules are evaporated from sample 102 due to the gas and heated ions of reagent 55 exiting the output of reagent ion generator 50 impinging on sample tube 101. Sample 102 is deposited and/or loaded into glass tube 101 mounted on sample holder 110. Molecules from the evaporated sample can be absorbed into charged electrospray liquid droplets. Sample ions are then formed as the charged liquid droplets evaporate, moving towards the nosepiece electrode 70 orifice against the heated countercurrent drying gas 60, forming ions as the charged droplet evaporation proceeds as is known in technique. Alternatively, reactant ions possibly with multiple charges formed from the electrospray droplets can exchange charge with molecules from the gas phase sample to form the sample ions which are directed to capillary orifice 30 and mass spectrometer 78 for mass analysis. /load, as described above. Sample molecules from the gas phase of sample 102 can be exposed to either reagent ions 55 exiting reagent ion generator 2 or reagent ions generated by electrospray or charged droplets individually or simultaneously. Selection of reagent ion source or charged drop is achieved by controlling the voltages applied to the corona or luminescent discharge needle 48 and electrospray needle 103 and by controlling fluid flow or nebulization and reagent gas sources 111, 58, 59, 87, 88 and 98.
    [0069] The sample gas can be introduced directly into the ionization region 84, where ionization occurs through charge exchange with reagent ions or metastable species formed from the corona or luminescent discharge source 47 or electrospray 103. The ions resulting from the sample are then routed to mass spectrometer 78 for mass/charge analysis, as described above. Referring to Figure 3, sample gas supply 114 delivers sample gas through gas flow tube 115 with sample gas exiting at proximal end 117 to ionization region 84. sample 114 may be, among others, a gas chromatograph, an ambient gas display or breathalyzer, positioned outside the sealed housing assembly 14.
    [0070] The heating of the sample is an important variable to control to achieve reproducible, consistent and reliable sample ionization efficiency. Different samples have different heating capacity and may require different temperatures to effect evaporation of the sample molecule. In some embodiments, the enthalpy required to heat a sample surface can be controllably delivered from multiple sources. A heat source applied to a sample surface is delivered as heated reagent ion gas from reagent ion generator 2, as described above. The amount of enthalpy delivered to the sample surface of the reagent ion and gas flow 55 exiting the output 50 of the reagent ion generator 2 is a function of the temperature and flow rate of the mixture of output gas and ion 55. gas and reactant ion is controlled by adjusting the temperature of heater 44 with some addition of heat from the corona discharge or luminescent 47. The total gas flow rate passing through the output 50 of reactant ion generator 2 is described above. Alternatively or in addition, the heating can also be delivered to a sample surface using a light source.
    [0071] Referring to Figures 1, 2, 4 and 5, the light source 7 includes, among others, an infrared light source, a white light source or a laser which, as shown in Figure 4, includes contacts electrical 120. Some heating light source embodiments 7 include a white or infrared light quartz lamp configured in a reflective envelope 121. The top end 122 of the internally reflective envelope 121 includes an approximate parabolic reflector and the output end 123 , internally molded as a reflective light concentrator as it is known in the sunlight collecting field. The output of the heating light source 124 can include a light concentrating lens, a large aperture, or an internally reflective light pipe, depending on analytical and sample needs. The heating light source 7 is mounted and positioned in the DSA ion source system 1 so that light 125 coming out of the heating light source 7 is cast on the sample being analyzed. The intensity of light falling on the sample surface is adjusted by controlling the voltage applied to the lamp electrodes 120 or the laser strength, if the light source 7 is a laser, and the size of the focused light spot. The light and heated reagent gas can be used individually or simultaneously to controllably heat a sample surface. Depending on the type and composition of the sample, controlled heating or heat gradients applied to a sample surface that includes a mixture of components can cause a separation in time or temperature of different sample components leaving the sample surface. Compost species with low evaporation temperatures evaporate from the sample surface before high evaporation temperature sample species. Creating a sample surface temperature ramp through a temperature gradient can achieve sample component separation in time. This temperature separation of sample species can reduce interferences in the ionization process, increase analytical peak capacity and allow some degree of selectivity with ion fragmentation in the capillary to separator region. Additional analytical information can also be obtained on the surface composition of the sample by monitoring species desorption as a function of temperature in a manner well-known to those skilled in the art of thermal desorption spectroscopy.
    [0072] The heating light source 7 can be configured with an output lens that focuses the emitted light at a smaller point on the sample surface that can be achieved using heated gas flow. This concentrated heat source allows for better spatial resolution on surfaces when analyzing solid phase samples or other types of samples. Referring to Figures 4 and 5, thin layer chromatography (TLC) plates 130 and 131 are mounted on the sample holder assembly 132 and held in place by a spring clip 133. A mixture of sample species is separated along the length of a thin layer chromatography plate, resulting in a row of spatially separated solid phase sample components. The thin layer chromatography plates 130 and 131, as mounted on the sample holder assembly 132, have sample separation lines running approximately perpendicular to the geometric axis of the nosepiece 13. One or more sample separation lines may be run on a single CCD card. To avoid cross talks between CCD channels on the same plate, concentrated application of heat is required with minimal superheat. The concentrated heating light 124 is directed to a sample channel separated by CCD as the sample holder assembly 132 moves the line of the CCD plate 130 in a direction perpendicular to the geometric axis of the objective holder electrode 13. The pyrometer 8 pointed at the heated point of sample 137 on the CCD plate 130 measures the surface temperature being directly heated by the heating light 125. The temperature measurement of the pyrometer 8 is responded to the control software to adjust the light intensity of the source. heat light 8 to maintain the sample surface temperature at sample location 137 at the desired set temperature. When the heating light source 7 includes an infrared light source, the lamp can be turned off briefly when taking a pyrometer measurement to avoid an error in surface temperature reading due to infrared light. The surface temperature of the sample can be measured directly with pyrometer 8 or alternatively with a thermocouple. Direct measurement of sample surface temperature with response to heating controls allows for more consistent, reliable and robust ion source performance when analyzing multiple samples of the same sample type, when analyzing sample surfaces such as plates of CCD or plant or animal tissue or when measuring different types of sample.
    [0073] The intensity of the heating or laser light 8 can be quickly adjusted because it is not subject to the heating capacity of a heating element as is the case with the reagent ion generator heater 44. The adjustment of the gas temperature of a reagent gas 55 leaving output channel 49 takes longer because of the heating capability of the total gas flow path in the reagent ion generator 2 and for the heating generated by the corona or luminescent discharge 47. Figure 4 shows the generator of Reagent ion 2 configured and positioned with outlet angled end 134 directing gas and ion flow through outlet 50 directly to sample point 137. The heated gas and ions 50 focusing on sample surface location 137 supplement heating more concentrated delivered to the surface of sample 137. Referring to Figure 5, the reagent ion generator 2 and angular output end 134 are rotated approximately 180° and move to along angular axis 135. The gas and reactant ions 50 flowing through outlet 50 are directed approximately parallel to location 137 of the sample surface. In the embodiment shown in Figure 5, luminous heater 7 delivers the primary source of enthalpy between sample surface location 137, allowing for tighter control of sample surface temperature and the size of the area being heated at sample location 137. In the modalities shown in Figures 4 and 5, pyrometer 8 is positioned to read the temperature of the location of the sample 137 being heated.
    [0074] The DSA ion source system 1 can be configured with a video camera 10 with or without a fiber optic probe 11. The correctly positioned video camera 10 can be used to view the location of the surface of the sample being analyzed and responds to the software or the user with the visual state of the surface at any time during the analysis. The translation agent control of the four-axis sample holder assembly 3 determines the precise location of a given sample surface relative to the capillary sampling hole 30 of the mass spectrometer 78. The known position of the sample is correlated to the spectral data of mass and can also be correlated to video images during sample analysis. The video camera 10 includes suitable optical light lenses to provide surface magnification of the samples. With the appropriate optics, video camera 10 can be configured outside of housing 14 to minimize exposure of video camera 10 to the sample environment and to reduce and/or eliminate any degassing of camera housing or electronics. Such degassing would add undesirable prior chemical species within the housing 14 of the DSA 1 ion source system.
    [0075] The angular reactant ion generator 2 shown in Figures 1 through 7 includes the swiveling angular end 134 with removable end piece 51 in shown in Figures 1, 2, 3, 6 and 7 and the swiveling reduced diameter end piece 140 shown in Figures 4 and 5. Referring to Figures 2 and 5, the geometry axis 141 of the reactant ion generator heater is angled from the axis 142 of the output end 134. The angle geometry of the reactant ion generator allows analysis of round, square, or other shaped sample holder sets where samples can be loaded along the entire outer edge without interfering with the reagent ion generator 2. For example, in Figure 1, the 20 sample holders , 21 and 22 are mounted along the outer edge of the square-shaped sample target assembly 3. As each sample 27 moves into position for analysis, no contact is made with the reagent ion generator 2 by any other atoms. rear mounted on the sample holder assembly 3. The angular geometry positions of the reagent ion generator 2 isolated the heater body 144 far enough from the loaded samples to prevent unwanted heating of the sample prior to or subsequent to each sample analysis. Due to the angular geometry of reagent ion generator 2 and the four geometric axes translation of sample holder 3, a greater variety of samples having different shapes and dimensions can be positioned and analyzed using a compact geometry of sample holder assembly 3 For example, the six-inch perimeter of the square sample holder assembly is twenty-four inches long. An equivalent linear geometry sample holder would be 24 inches long in one direction, but would require a 48 inch wide ion source to pass some or all of the samples in a line past the ionization region. The more compact geometry of sample holder assembly 3 with mounted samples arranged in three dimensions instead of two dimensions allows for the configuration of a smaller and more compact DSA 1 ion source and a correspondingly smaller housing 14.
    [0076] A smaller volume of DSA ion source 1 and housing 14 includes less volume to purge gas phase contaminants between each sample analysis and when loading and unloading sample holder assemblies 3 110, 132 and 162. use of gas is required to effectively purge a smaller volume from the source and less time is required to remove gaseous species of contamination before starting a new sample analysis set or between each sample analyzed. Faster purging of contaminant species allows for faster analysis times for multiple sets of ion source samples improving overall analytical efficiency.
    [0077] Referring to Figures 6 and 7, the geometry of the angular reagent ion generator 2 with swiveling output end assembly 134 allows for fast, automated positioning of the output 50 for optimal operation with different sample types. Reagent ion generator output 50 is positioned to provide maximum ionization efficiency for each sample type with high ion sampling efficiency for capillary port 30. Heater body 144 does not interfere with samples mounted on sample holder assemblies 3, 110, 132 and 162 shown in Figures 1, 3, 4 and 6 respectively. The linear and angular position of the body and heater output of the reagent ion generator 50 is adjusted with the four-axis translator assembly of the reagent ion generator 150. Reactant ion 150 that are shown in Figures 6 and 7 include horizontal linear axis 151, rotary axis 152, angular linear axis 153 and second rotary axis 154. Each axis can be manually adjusted or automatically adjusted with software-controlled motors driving each geometric axis. Different geometry axis of translation configurations may be substituted for the modality shown at 152 while retaining similar reduced or increased flexibility and function. Sensors can be added to measure the position of each geometric axis in a manual or automated translation agent assembly that provides the software with accurate positioning of reagent ion generator 2 relative to sample position and relative to fixed nosepiece position 13 As will be described in later sessions, the position sensor response on the position of the sample holder sets 3, 110, 132 and 162 and on the position of the reagent ion generator 2 to the software allows for automated and optimized positioning of the reagent ion generator and samples during analysis while avoiding contact with the surface and electrodes of the DSA1 ion source system.
    [0078] Figure 6 diagrams the reactant ion generator 2 in an elevated position with the angular linear axis 153 retracted and the angular output assembly 134 rotated to a position where the output 50 is pointed at an angle downward toward sample 160 held by a sample clamp 161 mounted on the movable sample holder assembly 162. As an example, sample 160 in Figure 6 may be a piece of orange peel where the analysis is run to determine which, if any, pesticides or fungicides are present in the orange peel. Figure 7 diagrams the reagent ion generator 2 at a lower position with the angular axis 153 extended and the rotary angular end assembly 134 rotated approximately 180 degrees from the position shown in Figure 6. The axis of the removable output piece 168 is positioned approximately horizontally to optimally ionize the grid sample 27 on the sample holder 20. In the embodiments shown in Figures 6 and 7, the angle of the heater body of the reagent ion generator 144 relative to the horizontal plane has not changed in the high and lower position. Connection 155 is secured to flexible connection 156 mounted to stationary section 164 of linear angular translator 150 and is secured to flexible connection 157 mounted to swivel ring 141 of swivel angle end assembly 134.
    [0079] Connection 155 causes the rotary angular end assembly 134 to rotate as the angular linear axis translator 153 moves from the retracted position to the extended position. The rotation of the angular end assembly 134 is reversed as the angle linear axis translator 153 moves from the extended to the retracted position. Alternatively, connection 155 with connections 158 and 157 can be replaced with a rack and pinion gear or worm gear assembly appropriately mounted on translation agent assembly 150 and output end assembly 134. Different models of connection assemblies or gear can be employed to automatically rotate the output end assembly 134 to achieve optimal placement for each type of sample. Outlet end assembly 134 may also be manually rotated for optimal positioning of outlet 50.
    [0080] The position of the reagent ion generator output 50 can be adjusted manually or automatically during acquisition to maximize the ion signal using the data response. The four axis translator 150 can be adjusted by the software based on the obtained mass spectral data and the response of the position sensor. Such mechanical regulation dependent on sample data and reagent ion generator positions can be automated using the appropriate algorithm. With such automated tuning algorithms, different sample types, shapes and sizes can be loaded and the sample and reagent ion generator positions can be automatically adjusted for optimal performance with little or no user intervention.
    [0081] The rotating angle end assembly of the reagent ion generator 134 includes the removable end piece 140 shown in figures 4 and 5 and 168 shown in figures 6 and 7. The exit inner diameter of the removable end piece 140 is reduced compared to the outlet inside diameter of the end piece 168. The smaller size end piece 140 delivers the heated gas and reactant ions in a smaller diameter stream which may be desirable for some sample types. For other sample types where the larger flow diameter of the heated gas and reactant ion is most ideal, the larger diameter endpiece 168 would be selected. Longer, shorter or different diameter end pieces may be interchangeable in the rotating angular end assembly 134 of reagent ion generator 2.
    [0082] One or more heating light sources 7 may be mounted on the rotating angular end assembly 134 which includes the rotating ring 141 so that the heating light 125 automatically remains oriented in the direction of the flow of heated reactant gas and ion 55 when end assembly 134 is rotated. Similarly, the pyrometer 8 can be mounted on the swiveling angular end assembly 134 positioned to point to the location of the sample incident by the heating light source 7 and the heated reagent gas and ions 55. Alternatively, one or more heating light sources 7 and one or more pyrometers 8 can be positioned independently of the position of the reagent ion generator 2 and translationally refer instead to the position of the sample and the fixed position nosepiece 13 with appropriate translationally adjustable mounting bracket sets.
    [0083] In some embodiments, the sample holder assemblies 3, 100, 132 and 162 shown in Figures 1, 3, 4 and 6, respectively, are mounted on the translation agent assembly with four geometric axes 180 shown in Figure 8, for automated placement and movement of samples. Some embodiments of such a sample holder assembly over the four axis translator assembly 180 are diagramed in Figures 8, 9 and 10. The four axis translator assembly 180 provides a full range of motion for the analyzing different types of specimen with one or more specimens mounted on three-dimensional specimen holder assemblies 3, 110, 132, 162, 181 and other specimen holder assembly configurations and modalities. The four axis translator assembly 180 includes the rotation axis 182, the horizontal linear translation axis 183, the rotation axis 184, and the vertical linear translation axis 185 of the sample holder assembly 181 The multi-axis swivel swivel assembly 188 extends from bottom base plate 189, through base plate 189 from sealed opening 191 to housing 187 similar to housing 14 diagramed in Figure 1. Translator components with four geometry axes 180 configured within housing 187 include metal or other inert materials to prevent gaseous molecules of prior contamination from interfering with sample analysis.
    [0084] In the embodiments shown in figures 8, 9 and 10, the horizontal linear translation axis 183 includes a rack gear 192 and a rotating pinion gear 193 to effect the horizontal linear translation of the sample holder assembly 181 or 190. slewing pinion gear 193 is mounted on the upper end of the middle shaft 301 in the shaft assembly 188. The rotation of the middle shaft is driven by the motor and sprocket assembly 315 connected via chain or sprocket 344 to the sprocket 313 of the middle axis. The 312 Horizontal Linear Translator Assembly slides through the 318 Linear Bearing Guides allowing for precision linear motion with low friction. Sprockets 195 and 197 are rotatably mounted to the horizontal translation rack assembly 312. sprocket 193 through sprocket 194. Chain 193 involves spring-loaded intermediate sprocket 195, driven sample holder sprocket 197, and driving sprocket 194. The lower sprocket of inner shaft 198 is driven through of the fixed chain or belt 310 by the motor and sprocket assembly 311. The rotation of the rotation axis 184 is effected by the rotation of the external shaft 302 driven by the motor assembly and the sprocket 320, connected through the drive chain or belt sprocket 321 to the lower sprocket of the outer shaft 322. Through bearings 324, the outer shaft 302 is mounted on the bearing block 327 which is in turn. z, mounted on the translation plate 328 of linear vertical axis 185. The movement of the vertical translation plate 328 is effected by turning the lead screw 330, driven by the motor and sprocket assembly 332 connected to the lower sprocket 331 of the screw feed through chain or toothed belt 334. Vertical translation plate 328 slides over rails 335 to effect low-friction precision movement. The rotation of the inner shaft 300 and the middle shaft 301 takes place over bearings 326 and 325, respectively, allowing for precision low-friction rotary motion.
    [0085] The Four Axis Sample Holder Translator Assembly 180 includes two rotation seals and a sliding rotation seal that provides a gastight seal across the base 189 of the envelope 187 during all four movements. geometry shafts while not creating detectable chemical contamination within the housing 187. The circular shaft seal 340 provides a sliding and rotary seal to the outer shaft 302. The shaft seal 341 provides a rotary seal against the middle shaft 301 and the shaft seal shaft 342 provides a pivot seal against inner shaft 300. The seal material includes teflon or other material that provides an effective gas-tight seal while having no contribution to prior gas phase contamination within the envelope 187. 188 four axes translation provides a wide range of rotational and linear motion that includes only circular slip and rotary gas-tight seals. No leaky or potentially sticky linear seals were used. The evaporated sample molecules are effectively trapped in the sealed envelope 187 and swept out of the vent port 344 for a safe laboratory ventilation system, preventing any exposure to the user. Conversely, contamination of the environment is prevented from entering enclosure 187 during analysis, thus providing operational and analytical benefits as described above.
    [0086] The 180 four geometric axes translator set provides the full range of motion required for sample surface profiling and shape, sample position verification, optimized analysis, loading and unloading of sample holder sets and to carry out the complete profiling of the sample holder plate to determine the type of sample holder, the type of sample, numbers, positions and heights before analysis. Figures 11 through 20 illustrate an automated progression of sample analysis, unloading an analyzed sample set, loading a new sample set, sensor profiling the new sample set, and analyzing the new sample set .
    [0087] Referring to Figure 11, the rounded sample holder assembly is loaded with a set of sample tablets that are sequentially analyzed by the rotating sample holder assembly with tablets passing in front of the nosepiece 13. The generator of reagent ion 2 is located with the output 50 in a downward angular position similar to that shown in Figure 6. Controlled heating of the samples is effected by the heated gas and reagent ions 55 and the heated light sources 7 with the sample temperature response of pyrometer 8 as described above. Position sensors 334, 345, 347, and 348 detect the position of each geometry axis of the translation agent assembly with four geometry axes of reagent ion generator 2, respectively, and respond to the precise position of reagent ion generator 2 for the software. Purge gas 353, typically nitrogen, flows through baseplate 185 to gas collector 351. Purge gas 352 flowing from gas collector 351 moves through the volume of ion source 354 within envelope 187 dragging the molecules evaporated from the sample out through the 344 vent after the 199 humidity sensor for a safe laboratory ventilation system. Purge gas 352 dragging evaporated sample molecules out of vent 344 minimizes cross-contamination between samples.
    [0088] In conjunction with the purge gas 352 flowing continuously, minimizing cross-contamination between samples can be achieved by moving the sample holder 3, 110, 132, 162, 190 or 371 to a position where the reagent ion generator exiting the gas stream 55 or any source of luminous heating does not impinge on the sample position or sample holder surface. For example, lowering the position of the sample holder assembly 190 in Figure 11 after running a sample prevents preheating the next sample to be analyzed although contamination from previous sample runs has a time to be swept out by the purge gas flow 352. In addition, increasing the intensity of the luminous heater 7 briefly and increasing the heated reagent gas flow 55 will drive the condensed sample species out of the nosepiece 13 surfaces and capillary electrode 12 surfaces. before analyzing the next sample. When the reagent ion generator 2 is positioned with the output 50 oriented in a downward position, the position of the reagent ion generator 2 can be quickly moved to provide a horizontal output position 50 between sample analysis. With the reagent ion generator output 50 oriented in a horizontal position, the heated reagent gas flow 55 and/or luminous heater 7 are directed towards the face of the objective port 13 and the capillary inlet electrode 12. Any contamination that may have accumulated in the objective port 13 or in the capillary inlet electrode 12 will be re-evaporated by this direct heating and the contamination molecules from the previous sample are dragged out by the countercurrent drying gas flow 70 and the purge gas flow 352 and the exit through vent 344 before running the next sample. The intensity of the luminous heater 7 and the flow rate of heated reagent gas flow 55 can be increased to accelerate the contamination molecule evaporation rate, effectively shortening the electrode cleaning time period. Mass spectra can be obtained during this cleaning and purging step to monitor the level of contamination or previous sample remaining. This purge step can be continued until the previous chemical noise in the acquired spectra has been reduced to an acceptable level using data dependent response algorithms or alternatively it can be continued for a programmed duration of time without data dependent response. When an acceptable reduction in the contamination or above signal is achieved, the intensity of the luminous heater 7 turned down and the flow of ion and heated reagent gas 55 is reduced to the ideal level for analysis. The sample holder assembly 190 is then moved to an ideal position for rotated analysis to present the next sample tablet for analysis. The sample analysis and contamination reduction steps between sample analysis can be programmed for automated operation through the software or conducted through manual control. Sample holders can be configured to provide regions where gaps in the specimen or specimen holder surface appear. The sample holder translation agent 180 can be moved into gaps in the sample holder between analyzes to conduct a purge or cleaning step. In this way, a sample support position requires minimal movement between sample analysis.
    [0089] Figure 12 shows a top view of housing 187 of the DSA ion source 1 during sample analysis which includes the sample holder assembly 190 with sample tablets 360 mounted in a pattern. A shield 358 covers the four axis drive assembly 180 and the multi axis assembly 188. The purge gas 352 flowing from the manifold 351 is directed to sweep the entire volume 354 within the housing 187.
    [0090] When some or all of the tablets 360 mounted on the sample holder assembly 190 are analyzed, the sample holder assembly 190 is moved to the unloaded position in the opening 364 of the sample loading and unloading region 363. purge gas flow 365 continues to drag through sample holder assembly 190 through gate 391 between sample holder 192 and opening 364 and drags out of vent port 344. sample 190 to its loaded and unloaded position, the four axis translator assembly 180 passes through or through position sensors 367, 350 and 368 to reestablish the reference location of the horizontal linear axis translation assembly 312 and the sample holder assembly 190 of rotation axis 182 respectively. The zero positions of the rotation axis and vertical linear axis of the translator with four geometric axes 185 are also revalidated by the position sensors located below the base plate 185 outside the envelope 187. Referring to Figure 13, when the sample holder assembly 190 is located in the opening 364, its position is precisely known and validated by the software. Figure 14 shows a top view of sample holder assembly 190 positioned in opening 364 just after discharge.
    [0091] Referring to Figure 15, the sample holder assembly 190 is removed from the housing 187 of the DSA ion source 1. The top cover 370 is opened together with the hinge 373 to facilitate both automated and manual removal of the holder assembly. of sample 190. The remaining sample reference plate 371, fixed to the translator with four geometric axes 180, includes mounting pins for the reference position 372. The purge gas 352 flowing from the collector 351 can be turned off to avoid exposing the user to any residual evaporated sample species still present within enclosure 187. Alternatively, if the source purge time is sufficient to clear the source of residual sample molecules from the gas phase before opening the top cover 370, then purge gas stream 365 can remain on to minimize or prevent ambient contamination from entering the DSA 354 source volume during charging or discharging watering of samples. Referring to Figure 16, new sample holder assembly 380 is loaded onto sample reference plate 371 in loading region 363. Sample holder assembly 380 includes sample tubes 382 with loaded powder samples 383 and the standard of the plate identifier hole 381. The reference alignment pins 372 and the top surface 384 of the sample reference plate 371 establish the precise position of the sample holder assembly 380 which is known to the software. The software has not yet validated how many samples have been loaded and what the specific positions and heights are for each sample. The 352 purge gas flow remains on or off depending on the user or preferred method.
    [0092] Referring to Figure 17, the top cover 370 is closed and seals when closed. The purge gas flow 352 from the gas manifold 351 that forms the purge gas flow 365 is turned on if it was previously turned off or remains on if the previous state was turned on during loading of the sample holder 380. purge gas 365 enters loading region 363 and exits through vent 344 which passes moisture sensor 199 to sample holder assembly with samples 383 down. Moisture sensor 199 configured in vent line 344 or alternatively positioned in the sample loading region 363 measures the moisture content of the output purge gas 365. Again the loaded sample holder 380 and samples 383 are dried by the purge gas 365 with moisture contact response provided to the software by the sensor. humidity 199. When the input humidity level is reduced to the desired level, the sample holder assembly 380 can be moved into the source volume DSA 354. Alternatively, may be preferred. o run liquid or wet samples in the case where pre-drying the sample with purge gas 365 would be minimized after sample loading. The purge region 363 and additional drying of samples, if necessary, with the moisture sensor response from the 199 moisture sensor provides a controlled means to consistently precondition samples prior to analysis. Controlled sample preparation and conditioning prior to analysis allows for consistency and improved reproducibility in sample evaluation.
    [0093] During this region 363 purge after the sample loading region, the reagent 2 ion generator remains on with the mass spectrum being obtained to check the previous chemical contamination level in DSA 354 Source Volume. The purge cycle Sample loading as described above may continue until the previous ambient signal is sufficiently reduced as determined by data-dependent response by mass spectral evaluation during the subsequent sample loading purge cycle. Calibration solution can be introduced into reagent ion generator 2 as described above to adjust and calibrate mass analyzer 78 before samples 383 are run. With continued purging, when the previous chemical noise level observed in the obtained mass spectrum has been reduced to an acceptable level and/or, if desired, the moisture level in the vent purge gas 365 is sufficiently low, the 371 sample with loaded 383 samples is diminished within the DSA 387 ion source region.
    [0094] Referring to Figures 18 and 19, the sample holder assembly 371 is moved under the distance measuring sensor 350. One modality of distance measuring sensor uses a laser beam and a light sensor to measure the height of objects moved under the sensor. The position of the sample holder assembly 371 is translated and rotated under the distance measurement sensor 350 and the hole pattern of the plate identifier 381 is mapped to identify the type of sample holder assembly 390. Alternatively the top surface 393 of the sample holder 380 may include a barcode 394 to identify the type of sample plate holder 380. The optical barcode reader 392 shown in Figures 12 and 19 is used to read the barcode 394 since sample holder 380 is translationally moved under bar code bed 392.
    [0095] Using the distance sensor 150 and the sample holder translator 180 the number, location and height of each sample tube 382 are mapped and combined with the list of samples loaded into the software. Using the sample holder plate identification and sample position mapping information generated by the distance measurement sensor 350 and the barcode reader 392, sent to the software and electronic controllers 82, the software adjusts the position of the generator Reagent ionic generator 2 and rotatable angle output assembly 134. The position of the motorized angled linear axis translator 153 is moved to its extended position in the reagent ionic generator four axis translator assembly as described for Figure 7. With the 344 position measurement sensor information response sent to the software, the software automatically checks the new probe position of the new reagent ion generator. Based on input from multiple sensors, the components of the DSA 1 ion source automatically adjust to provide optimal analysis of reloaded 382 sample tubes. previous gas known within envelope 187 before the start of sample analysis. Figure 19 shows a top view of DSA system 1 that includes a position measurement sensor 350 that is used to identify the type of sample holder assembly 390 and to map the sample positions of the reloaded sample holder assembly 390 Alternatively, in addition, the DSA system 1 includes a barcode reader 392 to identify the type of sample holder assembly 390.
    [0096] The distance sensor 150 can be used to map the contour of sample surfaces that enables software algorithms to establish the ideal position of the sample for analysis. The four axis translator 180 moves a sample under the laser beam of the distance sensor 150 to produce a map of the surface elevations and edges of the sample. For example, if an orange peel is loaded into the DSA ion source system 1, as shown in figure 6 held by clamp 161, the surface and edges are mapped using the distance sensor 150. The sample is then ideally positioned with respect to orifice 30 inside vacuum to maximize sensitivity and prevent the sample from contacting the “objective port” (nose piece) 13 or the removable end piece of the reagent ion generator 51. In addition, the position of the reagent ion generator 2 can be established with respect to the sample to provide optimal sample ionization conditions. Each sample can be profiled using the distance sensor 150 or additional sensors from which its position can be optimized for analysis automatically over a sample through the sample base.
    [0097] With reference to figure 20, after the reloaded sample holder assembly 390 has been identified and some or all of the loaded sample positions 383 have been mapped, the sample holder assembly is moved to the ideal position to drive sample analysis of samples loaded 383 by the translator with four geometric axes 180. In addition, the reagent 2 ion generator was ideally positioned automatically via software control to conduct sample analysis. Purge gas 352 remains on during sample analysis 382 to minimize purge cycles that employ transfer of sample contamination between sample analysis as described above. For example, sample holder assembly 390 can be lowered or moved to a position between samples after analyzing a sample to reduce the pre-transfer of sample contamination as described above to pre-sample holder assembly 190.
    [0098] The DSA ion source system 1 can be configured with means to generate sample ions without the need for the reagent ion generator 2. Referring to figure 21, the modified DSA 400 ion source includes fluid delivery needle 103, the sample holder assembly connected to the translation agent assembly with four geometric axes 180, paper or polymer sample sprayers 402 with sample stained on each sprayer, sample sprayer holder 403, syringe pumps 58 and 59 configured with syringes 60 and 61 respectively and the objective port 13 with capillary inlet electrode 12 as previously described above. Voltages applied to objective port electrode 13 and capillary inlet electrode 12 sustain the electrospray of each sprayer 402. Liquid droplets 404 can be delivered from needle 103 to sample spot sprayer 402 during electrospray to move the smeared sample toward spray tip 405 of spray 402. The solution composition and fluid flow rate that are delivered through needle 103 to spray 402 during electrospray are controlled using syringe pumps 58 and 59 with syringe 60 and 61 respectively.
    [0099] Figure 22 shows a mass spectrum in ion-positive polarity mode when turmeric powder was heated in the DSA 1 ion source using a glass tube sample holder similar to the 382 sample tubes shown in Figures 3, 16 and 20. Figure 23 shows three mass spectra obtained in the positive ion polarity mode from three cooking oil oil samples run in the DSA 1 ion source. The liquid cooking oil was evaporated from the removed tips. of the glass tubes after the cooking oils have been drained into small glass spikes. Figure 24 shows the mass spectrum obtained in the positive and negative ion polarity mode of liquid Diet Coca samples run on the DSA 1 ion source loaded onto the mesh targets similar to the mesh set 22 shown in Figure 2. Figure 25 shows three mass spectra of solid chili pepper plant samples performed with no sample propaedeutics on the DSA 1 ion source. The peak height amplitude of capsaicin increases the stinging of the analyzed pepper. Capsaicin is the primary component that makes pepper taste spicy.
    [00100] Several embodiments of the invention have been described. However, it will be understood that various modifications can be made without departing from the spirit and scope of the invention. Accordingly, other embodiments are within the scope of the following claims.
    权利要求:
    Claims (15)
    [0001]
    1. Apparatus (1) for analyzing chemical species, characterized in that it comprises: a housing (14) for operating at approximately atmospheric pressure during operation of the apparatus (1); a reagent ion or metastable species generator (2) comprising: a corona or glow discharge needle (48), positioned in the housing (14), which produces a corona or glow discharge during operation of the apparatus (1) to generate a reactant ion or metastable species; a swiveling angled end (134) and a removable end piece (51); at least one seal configured to prevent gas exchange with ambient air during sample analysis within the housing (14); a sample holder assembly (3) mounted on a translation stage positioned in the housing (14), the sample holder assembly (3) comprising at least one sample holder (20-22) comprising a plurality of sample locations individual; and a gas phase detector (78) for detecting and analyzing a chemical species of ionized sample during operation of the apparatus (1); and a capillary (80) configured to direct chemical species of ionized sample to the gas phase detector (78), where during operation of the apparatus (1), the stable ion or metastable species generator (2) ionizes sample chemical species positioned at a corresponding sample location to generate ionized sample chemical species.
    [0002]
    2. Apparatus (1) according to claim 1, characterized in that the flow of steam or gas from the reagent ionic generator (2) is configured to flow through the corona or glow discharge needle (48).
    [0003]
    3. Apparatus (1) according to claim 1, characterized in that one or more chemical species of sample comprise solid, liquid or gas phase samples or emulsions or powder samples.
    [0004]
    4. Apparatus (1) according to claim 1, further comprising providing a sample gas (114) to introduce a flow of sample gas into the housing (14).
    [0005]
    5. Apparatus (1) according to claim 1, characterized in that the capillarity (80) further comprises an orifice (30) having a voltage applied to it during operation of the apparatus (1).
    [0006]
    Apparatus (1) according to claim 1, characterized in that it further comprises at least one gas flow controller (93), at least one gas heater (62) and at least one temperature control (7,8 ).
    [0007]
    7. Apparatus (1) according to claim 1, characterized in that the plurality of individual sample locations is configured in a two-dimensional array.
    [0008]
    8. Apparatus (1) according to claim 1, characterized in that the sample holder assembly (3) comprises a plurality of sample holders (20-22).
    [0009]
    9. Apparatus (1) according to claim 8, characterized in that two of the plurality of sample holders (20-22) are arranged in intersecting planes.
    [0010]
    10. Apparatus (1) according to claim 1, characterized in that the swiveling angular end (134) is configured to be disposed close to at least one sample holder (20-22).
    [0011]
    Apparatus (1) according to claim 10, characterized in that it further comprises a position sensor (334, 345, 347, 348) for at least one sample holder (20-22), wherein during operation of the apparatus (1), the position sensor (334, 345, 347, 348) provides a response to allow automatic and optimized positioning of the reagent ion generator or metastable species (2) relative to at least one sample holder (20- 22).
    [0012]
    Apparatus (1) according to claim 1, characterized in that it further comprises a heating source (7) configured to apply controlled heating or heat gradient to a sample surface (137) of at least one sample holder ( 20-22) to cause separation in time or temperature of different sample components leaving the sample surface (137).
    [0013]
    13. Apparatus (1) according to claim 1, characterized in that at least one sample holder (20-22) comprises mesh targets (24) configured to hold liquid samples.
    [0014]
    14. Apparatus (1) according to claim 1, characterized in that at least one sample holder (20-22) comprises a substrate having two parallel surfaces, one of the parallel surfaces being positioned adjacent to the reagent ion generator or metastable species (2), and the other of the two parallel surfaces being positioned adjacent to an inlet (30) of the capillary (80).
    [0015]
    15. Apparatus (1) according to claim 4, characterized in that during the operation of the apparatus (1), the sample gas flow charge exchanges with the reagent ions or metastable species formed from the corona or glow discharge.
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    同族专利:
    公开号 | 公开日
    CA2837478A1|2012-12-06|
    CA2837478C|2019-02-26|
    EP2715772A1|2014-04-09|
    CN103797559B|2016-09-28|
    WO2012167183A1|2012-12-06|
    EP2715772A4|2015-04-01|
    EP2715772B1|2016-08-10|
    CN103797559A|2014-05-14|
    US9240311B2|2016-01-19|
    BR112013031106A2|2016-12-06|
    AU2012261885B2|2015-09-24|
    US20120312980A1|2012-12-13|
    AU2012261885A1|2013-12-12|
    JP6182705B2|2017-08-23|
    JP2014517481A|2014-07-17|
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    法律状态:
    2018-12-11| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|
    2019-10-29| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]|
    2021-04-06| B06A| Notification to applicant to reply to the report for non-patentability or inadequacy of the application [chapter 6.1 patent gazette]|
    2021-06-01| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|
    2021-06-22| B16A| Patent or certificate of addition of invention granted|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 01/06/2012, OBSERVADAS AS CONDICOES LEGAIS. |
    优先权:
    申请号 | 申请日 | 专利标题
    US201161493255P| true| 2011-06-03|2011-06-03|
    US61/493,255|2011-06-03|
    PCT/US2012/040587|WO2012167183A1|2011-06-03|2012-06-01|Direct sample analysis ion source|
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