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Sample records for accelerator mass spectrometer

  1. The AMS [Accelerator Mass Spectrometer] program at LLNL

    Livermore will have an operational Accelerator Mass Spectrometer (AMS) by mid-1989 as part of its new Multi-user Tandem Laboratory. The spectrometer was designed primarily for applications in archaeology and the geosciences and was co-funded by the University of California Regents. Radiological control for personnel protection, ion sources and injection systems, the tandem and all beam handling hardware are operated with a distributed processor computer control system. The Tandem is the former University of Washington injector FN which has been upgraded with Dowlish tubes, pelletron charging and SF6 gas. Design goals for the AMS system, computer aided operation, automated measurement capability, initial results and some of our intended applications will be presented. 5 refs., 2 figs

  2. Installation of a tandem-type accelerator mass spectrometer

    Mizushima, Toshihiko; Togawa, Orihiko; Mizutani, Yoshihiko [Japan Atomic Energy Research Inst., Mutsu, Aomori (Japan). Mutsu Establishment; Kabuto, Shoji [Mutsu Marine Laboratory, Japan Marine Science Foundation, Mutsu, Aomori (Japan); Yamamoto, Tadatoshi [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    2000-02-01

    Tandem-type accelerator mass spectrometer (hereinafter referred to as Tandetron) was installed at the Ominato Facility of Mutsu Establishment, JAERI in April, 1997. The objective of its installation is to investigate the mechanism of the mixing and circulation of seawater in the ocean, by collecting seawater samples around Japan and analyzing the horizontal and vertical distributions of {sup 14}C contained in the samples. The Tandetron consists of two lines to measure isotopic ratios of carbon and those of heavier iodine. The adjustment for the carbon line was finished and the measurements of seawater samples were started. The iodine line, on the other hand, is on the final step of its adjustment and performance tests are being carried out with a TOF (Time of Flight) detector. The iodine line will be used to analyze {sup 129}I released from a spent nuclear fuel reprocessing plant and other nuclear facilities. In this report, we summarize the status of installation of the carbon and iodine lines for the Tandetron. The report describes the situations of their adjustments until now, the outline of the Tandetron, tests of measurement performance, evaluation and inspection of shielding performance, problems and their solutions, and so on. (author)

  3. The distributed control system of Shanghai mini-cyclotron accelerator mass spectrometer (SMCAMS)

    It is mainly introduced the composition, structure, hardware and software designing, function, and the method of communication between the host computer and the ADAM modules of the distributed control system on Shanghai Mini-cyclotron Accelerator Mass Spectrometer (SMCAMS). Some detail problems such as controlling the devices staying on high voltage by ADAM-4541 (RS-485 to Fiber Optic Convertor) and optical fiber are also introduced

  4. Performance of the rebuilt SUERC single-stage accelerator mass spectrometer

    Shanks, Richard P.; Ascough, Philippa L.; Dougans, Andrew; Gallacher, Paul; Gulliver, Pauline; Rood, Dylan H.; Xu, Sheng; Freeman, Stewart P. H. T.

    2015-10-01

    The SUERC bipolar single-stage accelerator mass spectrometer (SSAMS) has been dismantled and rebuilt to accommodate an additional rotatable pre-accelerator electrostatic spherical analyser (ESA) and a second ion source injector. This is for the attachment of an experimental positive-ion electron cyclotron resonance (ECR) ion source in addition to a Cs-sputter source. The ESA significantly suppresses oxygen interference to radiocarbon detection, and remaining measurement interference is now thought to be from 13C injected as 13CH molecule scattering off the plates of a second original pre-detector ESA.

  5. Performance report for the low energy compact radiocarbon accelerator mass spectrometer at Uppsala University

    Salehpour, M.; Håkansson, K.; Possnert, G.; Wacker, L.; Synal, H.-A.

    2016-03-01

    A range of ion beam analysis activities are ongoing at Uppsala University, including Accelerator Mass Spectrometry (AMS). Various isotopes are used for AMS but the isotope with the widest variety of applications is radiocarbon. Up until recently, only the 5 MV Pelletron tandem accelerator had been used at our site for radiocarbon AMS, ordinarily using 12 MeV 14,13,12C3+ ions. Recently a new radiocarbon AMS system, the Green-MICADAS, developed at the ion physics group at ETH Zurich, was installed. The system has a number of outstanding features which will be described. The system operates at a terminal voltage of 175 kV and uses helium stripper gas, extracting singly charged carbon ions. The low- and high energy mass spectrometers in the system are stigmatic dipole permanent magnets (0.42 and 0.97 T) requiring no electrical power nor cooling water. The system measures both the 14C/12C and the 13C/12C ratios on-line. Performance of the system is presented for both standard mg samples as well as μg-sized samples.

  6. Design of virtual double-parameter multichannel analyzer to measure 14C on the accelerator mass spectrometer

    The author introduces the design of the virtual double-parameter multichannel analyzer based on PC DAQ board and LabVIEW, the graphical development platform, and the use of it to measure the double-parameter ΔE-Er spectrum of 14C on the accelerator mass spectrometer

  7. 129I level in seawater near a nuclear power plant determined by accelerator mass spectrometer

    129I concentration in the seawater samples near a nuclear power plant was determined in the Xi'an Accelerator Mass Spectrometer (AMS) Center. Isotope dilution method was used via addition of excessive amount of stable iodine (127I) in the sample before separation, and iodine in the seawater was separated by solvent extraction, and the back extracted iodine in iodide form was precipitated as AgI, which was used as AMS target for 129I measurement. 125I tracer was added to monitor the recovery of iodine in the whole separation process. 129I/127I ratios in the prepared target were determined by AMS. The concentration of 127I in seawater samples was determined by inductively coupled plasma mass spectrometry. The results show that the 129I/127I atomic ratios in the seawater range from 8.29x10-11 to 9.45x10-10, approximately one order of magnitude higher than that in seaweed collected in the pre-nuclear era, but fall in the environmental level of global fallout.

  8. Mass Spectrometer Studies of Ion Sources for One Shot AcceleratorTube

    Brumbaugh, R.; Pon, W.; Seaman, W.; Wiegand, C.

    1951-12-12

    A simple mass spectrometer using 60 degree focusing was set up to study the (illegible) of the ions produced by various types of sources. A schematic diagram of the apparatus is shown in Fig. 1, which is to a large extent self-explanatory. The isolation transformer was simply a piece of RG (illegible) cable about three feet long and was used in order to operate the source at high accelerating voltage allowing the collector to be at essentially ground potential. The collimating slits were 0.05 (illegible) wide and were space 4 (illegible-cm?) apart. The coarse slit immediately preceding the collector cup was 0.3 (illegible) wide. The electrometer was the integrating type which indicated the potential due to the charge collected on known capacitance. The vacuum tube voltmeter indicated the potential of the 0.5 (illegible) capacitor due to the total charge reaching the slit system. It thus served as a monitor of the source output for each firing. The neon lamp was a protection for the condenser against breakdown discharges of the tube.

  9. Cyclotrons as mass spectrometers

    Clark, D.J.

    1984-04-01

    The principles and design choices for cyclotrons as mass spectrometers are described. They are illustrated by examples of cyclotrons developed by various groups for this purpose. The use of present high energy cyclotrons for mass spectrometry is also described. 28 references, 12 figures.

  10. Cyclotrons as mass spectrometers

    The principles and design choices for cyclotrons as mass spectrometers are described. They are illustrated by examples of cyclotrons developed by various groups for this purpose. The use of present high energy cyclotrons for mass spectrometry is also described. 28 references, 12 figures

  11. Automated transportable mass spectrometer

    The need has been identified for a Mass Spectrometer (MS) which can be conveniently transported among several facilities for rapid verification of the isotopic composition of Special Nuclear Material. This requirement for a light weight, transportable MS for U and Pu mass analysis was met by deleting the gas chromatograph (GC) portions of a Hewlett-Packard (H-P) Model 5992 Quadrupole GCMS and substituting a vacuum lock sample entry system. A programmable power supply and vacuum gauge were added and circuitry modifications were made to enable use of the supplied software. The single rhenium filament plug-in source is loaded with either a nominal microliter of sample solution and evaporated, or with a prepared resin bead. Using a resin bead in a specially dimpled filament, copious sensitivity is obtained with 30 nanogram uranium samples. After sample insertion the analysis is completely controlled by an H-P Model 9825 calculator. Source vacuum of 2 x 10-7 torr or better is regained within 2 minutes after sample insertion, and total time for a complete analysis is about 7 minutes. Accuracy is better than 1% for isotope ratios less than 20 and better than 2% for ratios of 100. Ions are accelerated at about 1.8 volts into the mass filter which has pole pieces of hyperbolic cross section. Collection is by a Galileo Channeltron multiplier into a log preamp. During a normal run, 1.4 x 106 data point are observed and averaged. Weight of the instrument excluding the calculator is 88 Kg which allows relatively easy transportation over short distances by two persons. The instrument can be carried into a facility and be ready to analyze samples in less than 3 hours

  12. Magnetron mass spectrometer

    A magnetron mass-spectrometer characterized by increased sensitivity at low power is described. The mass-spectrometer contains ion source cylindrical analyzer located on its axis, ion collector and magnetic system. For decreasing consumed power the ion source is fixed at the end of the analyzer and it represents two coaXial cylinders located between plane electrodes, in one of which a ring slot takes place and the other one is connected with positive terminal of discharge voltage source. The magnetic system represents ring-form magnets fixed by similar poles to each other and separated by washers of magnetic-soft material, the washers being placed in the plane of the ion source. The analyzed ions in the described mass-spectrometer are obtained mainly at the expense of resonance recharge that increases accuracy of measurements due to decrease of fragment peak intensity

  13. Mass spectrometers: instrumentation

    Cooks, R. G.; Hoke, S. H., II; Morand, K. L.; Lammert, S. A.

    1992-09-01

    Developments in mass spectrometry instrumentation over the past three years are reviewed. The subject is characterized by an enormous diversity of designs, a high degree of competition between different laboratories working with either different or similar techniques and by extremely rapid progress in improving analytical performance. Instruments can be grouped into genealogical charts based on their physical and conceptual interrelationships. This is illustrated using mass analyzers of different types. The time course of development of particular instrumental concepts is illustrated in terms of the s-curves typical of cell growth. Examples are given of instruments which are at the exponential, linear and mature growth stages. The prime examples used are respectively: (i) hybrid instruments designed to study reactive collisions of ions with surfaces: (ii) the Paul ion trap; and (iii) the triple quadrupole mass spectrometer. In the area of ion/surface collisions, reactive collisions such as hydrogen radical abstraction from the surface by the impinging ion are studied. They are shown to depend upon the chemical nature of the surface through the use of experiments which utilize self-assembled monolayers as surfaces. The internal energy deposited during surface-induced dissociation upon collision with different surfaces in a BEEQ instrument is also discussed. Attention is also given to a second area of emerging instrumentation, namely technology which allows mass spectrometers to be used for on-line monitoring of fluid streams. A summary of recent improvements in the performance of the rapidly developing quadrupole ion trap instrument illustrates this stage of instrument development. Improvements in resolution and mass range and their application to the characterization of biomolecules are described. The interaction of theory with experiment is illustrated through the role of simulations of ion motion in the ion trap. It is emphasized that mature instruments play a

  14. Effective mass spectrometer

    The history and major accomplishments of the Effective Mass Spectrometer (EMS) are described. In the eight years since the EMS turned on, 21 experiments have been completed by groups from nine institutions in 32 months of operation. Over 400 million triggers have been recorded on magnetic tape, resulting in 29 journal publications to date. A list of experimental proposals for the EMS and a sampling of results are presented. 12 figures, 4 tables

  15. In Situ Mass Spectrometer Project

    National Aeronautics and Space Administration — The In Situ Mass Spectrometer projects focuses on a specific subsystem to leverage advanced research for laser-based in situ mass spectrometer development...

  16. Improvements to mass spectrometers

    This invention concerns mass spectrometers and, specifically, an ion beam analyser that facilitates the use of these spectrometers. Its object is to provide an improved apparatus for determining the desorption characteristics by field effect of a sample. It also aims to provide an improved system for carrying out sample analyses by using field effect desorption. Under the invention, facilities are added to the analyser to put out of action a part at least of the separation facilities so that the ion beam coming from the source of ions is not deflected. Detection means are located along the non deflected ion beam to detect the ions of the sample when they effectively appear and finally, actuating facilities are coupled to the out-of-action system so that the mass separation facilities may be brought back into action. This enables the operator to vary the parameters, such as the position of the source (emitter), the temperature and the electric field intensity until ions are released by the unknown sample

  17. Implementation of a mass spectrometer operating in the external beam of a proton accelerator. Application to the study of short-lived isotopes produced by uranium fission

    Implementation and use of a mass spectrometer operating directly in the external beam of a proton accelerator has proven to be a very fruitful way to study short-lived nuclides in both areas covered: measuring production cross sections and nuclear spectroscopy. The results obtained in this work are only a first step and can be developed in different directions in which the study was discussed and an extension to elements other than alkali may be considered. (author)

  18. A new LabVIEW-based control system for the Naval Research Laboratory Trace Element Accelerator Mass Spectrometer

    A new LabVIEW-based control system for the existing tandem accelerator and new AMS components has been implemented at the Trace Element Accelerator Mass Spectrometry (TEAMS) facility at the Naval Research Laboratory. Through the use of Device Interfaces (DIs) distributed along a fiber optic network, virtually every component of the accelerator system can be controlled from any networked computer terminal as well as remotely via modem or the internet. This paper discusses the LabVIEW-based control software, including remote operation, automatic calculation of ion optical component parameters, beam optimization, and data logging and retrieval

  19. High-resolving mass spectrographs and spectrometers

    Wollnik, Hermann, E-mail: hwollnik@gmail.com [New Mexico State University, Department of Chemistry & Biochemistry (United States)

    2015-11-15

    Discussed are different types of high resolving mass spectrographs and spectrometers. In detail outlined are (1) magnetic and electric sector field mass spectrographs, which are the oldest systems, (2) Penning Trap mass spectrographs and spectrometers, which have achieved very high mass-resolving powers, but are technically demanding (3) time-of-flight mass spectrographs using high energy ions passing through accelerator rings, which have also achieved very high mass-resolving powers and are equally technically demanding, (4) linear time-of-flight mass spectrographs, which have become the most versatile mass analyzers for low energy ions, while the even higher performing multi-pass systems have only started to be used, (5) orbitraps, which also have achieved remarkably high mass-resolving powers for low energy ions.

  20. High-resolving mass spectrographs and spectrometers

    Wollnik, Hermann

    2015-11-01

    Discussed are different types of high resolving mass spectrographs and spectrometers. In detail outlined are (1) magnetic and electric sector field mass spectrographs, which are the oldest systems, (2) Penning Trap mass spectrographs and spectrometers, which have achieved very high mass-resolving powers, but are technically demanding (3) time-of-flight mass spectrographs using high energy ions passing through accelerator rings, which have also achieved very high mass-resolving powers and are equally technically demanding, (4) linear time-of-flight mass spectrographs, which have become the most versatile mass analyzers for low energy ions, while the even higher performing multi-pass systems have only started to be used, (5) orbitraps, which also have achieved remarkably high mass-resolving powers for low energy ions.

  1. Biopolymer mass spectrometer with cryogenic particle detectors

    A novel type of biopolymer mass spectrometer is proposed for massive proteins, polypeptides and DNA-fragments by replacing standard ionizing detectors with cryogenic particle detectors. The detection efficiency in ionizing detectors decreases rapidly with increasing biopolymer mass owing to the biopolymer's decreasing velocity. Cryogenic particle detectors, however, record the total kinetic energy deposited by the accelerated biopolymer. In a given electric acceleration field, this kinetic energy is independent of mass and depends only on the biopolymer's charged state. Using the intrinsic properties of cryogenic particle detectors and their specific fabrication techniques, a mass spectrometer has been designed specifically for high-throughput DNA-sequencing. The calculated DNA-fragment separation rate would be increased by several orders of magnitude as compared to standard gel-electrophoresis DNA-sequencers. (orig.)

  2. Imaging mass spectrometer with mass tags

    Felton, James S.; Wu, Kuang Jen J.; Knize, Mark G.; Kulp, Kristen S.; Gray, Joe W.

    2013-01-29

    A method of analyzing biological material by exposing the biological material to a recognition element, that is coupled to a mass tag element, directing an ion beam of a mass spectrometer to the biological material, interrogating at least one region of interest area from the biological material and producing data, and distributing the data in plots.

  3. Advanced Mass Spectrometers for Hydrogen Isotope Analyses

    Chastagner, P.

    2001-08-01

    This report is a summary of the results of a joint Savannah River Laboratory (SRL) - Savannah River Plant (SRP) ''Hydrogen Isotope Mass Spectrometer Evaluation Program''. The program was undertaken to evaluate two prototype hydrogen isotope mass spectrometers and obtain sufficient data to permit SRP personnel to specify the mass spectrometers to replace obsolete instruments.

  4. New schemes of static mass spectrometers

    Different possibilities to increase the 'quality', or Q-quantity, of static mass spectrometers by expanding the ion beam before it enters the magnetic field are analyzed. The design of mass spectrometers using a cone-shaped achromatic prism is discussed. Different variants of achromatic mass spectrometers using electrostatic prisms and sector magnetic fields are also considered.

  5. New schemes of static mass spectrometers

    Baisanov, O.A. [Military Institute of Air Defense Forces, Aktobe (Kazakhstan); Doskeyev, G.A. [Aktobe State University named after K. Zhubanov, Aktobe (Kazakhstan); Spivak-Lavrov, I.F., E-mail: baisanov@mail.ru [Aktobe State University named after K. Zhubanov, Aktobe (Kazakhstan)

    2011-07-21

    Different possibilities to increase the 'quality', or Q-quantity, of static mass spectrometers by expanding the ion beam before it enters the magnetic field are analyzed. The design of mass spectrometers using a cone-shaped achromatic prism is discussed. Different variants of achromatic mass spectrometers using electrostatic prisms and sector magnetic fields are also considered.

  6. AixMICADAS, the accelerator mass spectrometer dedicated to 14C recently installed in Aix-en-Provence, France

    Bard, Edouard; Tuna, Thibaut; Fagault, Yoann; Bonvalot, Lise; Wacker, Lukas; Fahrni, Simon; Synal, Hans-Arno

    2015-10-01

    A compact AMS system dedicated to measuring 14C in ultra-small samples was installed at the CEREGE in Aix-en-Provence at the end of March 2014, together with an automated graphitization system. AixMICADAS operates at around 200 kV with carbon ion stripping in helium leading to a transmission of about 47%. The hybrid ion source works with graphite targets and CO2 gas. It is coupled to a versatile gas interface system that ensures stable gas measurements from different sources: a cracker for CO2 in glass ampoules, an elemental analyzer for combusting organic matter and an automated system to handle carbonate by wet chemistry. The analyses performed during the first half-year of operation show that a precision of about 2‰ is reached on modern samples of about 1 mg of carbon. Measurements of IAEA reference materials of various 14C ages show a good agreement with consensus values. Direct measurements of geological graphites indicate a machine background equivalent to an age of 68,000 years BP. AixMICADAS is thus limited solely by the 14C contamination of samples in the field and in the laboratory. The performances of the gas ion source and its gas interface system were tested with two CO2 production units: the elemental analyzer and the automated carbonate hydrolysis unit. These tests show that samples ranging between 10 and 100 μg C can produce a 12C- ion beam of the order of 10-15 μA during time spans ranging from 3 to 30 min depending on the sample mass. Coupling the automated hydrolysis system to the gas ion source of AixMICADAS, enables us to develop a method involving sequential leaching of carbonate samples with direct 14C measurements of the leached fractions and the residual sample. The main advantage is that all of steps leaching and hydrolysis are performed in the same vial for a particular sample. A sequential leaching was applied to a young carbonate sample (ca. 6600 years BP) whose 14C age agrees with previous determination and which shows no sign of

  7. Multidetector calibration for mass spectrometers

    The International Atomic Energy Agency's Safeguards Analytical Laboratory has performed calibration experiments to measure the different efficiencies among multi-Faraday detectors for a Finnigan-MAT 261 mass spectrometer. Two types of calibration experiments were performed: (1) peak-shift experiments and (2) peak-jump experiments. For peak-shift experiments, the ion intensities were measured for all isotopes of an element in different Faraday detectors. Repeated measurements were made by shifting the isotopes to various Faraday detectors. Two different peak-shifting schemes were used to measure plutonium (UK Pu5/92138) samples. For peak-jump experiments, ion intensities were measured in a reference Faraday detector for a single isotope and compared with those measured in the other Faraday detectors. Repeated measurements were made by switching back-and-forth between the reference Faraday detector and a selected Faraday detector. This switching procedure is repeated for all Faraday detectors. Peak-jump experiments were performed with replicate measurements of 239Pu, 187Re, and 238U. Detector efficiency factors were estimated for both peak-jump and peak-shift experiments using a flexible calibration model to statistically analyze both types of multidetector calibration experiments. Calculated detector efficiency factors were shown to depend on both the material analyzed and the experimental conditions. A single detector efficiency factor is not recommended for each detector that would be used to correct routine sample analyses. An alternative three-run peak-shift sample analysis should be considered. A statistical analysis of the data from this peak-shift experiment can adjust the isotopic ratio estimates for detector differences due to each sample analysis

  8. The Varian MAT-250 mass spectrometer. Steady isotopes laboratory

    This work treats over the performance and applications of the Varian Mat-250 mass spectrometer which is in the environmental isotope laboratory. It can be applied over topics such as: ions formation, acceleration and collimation, ions separation, ions detection, data transformation, sampling, δ notation. (Author)

  9. Low Power Mass Spectrometer employing TOF Project

    National Aeronautics and Space Administration — A low power Mass Spectrometer employing multiple time of flight circuits for parallel processing is possible with a new innovation in design of the Time of flight...

  10. Mass Spectrometer for Airborne Micro-Organisms

    Sinha, M. P.; Friedlander, S. K.

    1986-01-01

    Bacteria and other micro-organisms identified continously with aid of new technique for producing samples for mass spectrometer. Technique generates aerosol of organisms and feeds to spectrometer. Given species of organism produces characteristic set of peaks in mass spectrum and thereby identified. Technique useful for monitoring bacterial makeup in environmental studies and in places where cleanliness is essential, such as hospital operating rooms, breweries, and pharmaceutical plants.

  11. Time of flight spherotron mass spectrometer

    The possibility of using the spherotron, the mass spectrometer with crossed spherical electric and inhomogeneous magnetic fields, as a TOF mass spectrometry instrument has been analyzed. The possibility of achieving triple isochronous focusing has been shown. The estimates for the mass dispersion and resolutions are derived. (author)

  12. Evaluation of Small Mass Spectrometer Systems

    Arkin, C. Richard; Griffin, Timothy P.; Ottens, Andrew K.; Diaz, Jorge A.; Follistein, Duke W.; Adams, Fredrick W.; Helms, William R.; Voska, N. (Technical Monitor)

    2002-01-01

    Various mass analyzer systems were evaluated. Several systems show promise, including the Stanford Research Systems RGA-100, Inficon XPR-2, the University of Florida's Ion Trap, and the Compact Double Focus Mass Spectrometer. Areas that need improvement are the response time, recovery time, system volume, and system weight. Future work will investigate techniques to improve systems and will evaluate engineering challenges.

  13. ELECTRONICS UPGRADE OF HIGH RESOLUTION MASS SPECTROMETERS

    Mcintosh, J; Joe Cordaro, J

    2008-03-10

    High resolution mass spectrometers are specialized systems that allow researchers to determine the exact mass of samples to four significant digits by using magnetic and electronic sector mass analyzers. Many of the systems in use today at research laboratories and universities were designed and built more than two decades ago. The manufacturers of these systems have abandoned the support for some of the mass spectrometers and parts to power and control them have become scarce or obsolete. The Savannah River National Laboratory has been involved in the upgrade of the electronics and software for these legacy machines. The Electronics Upgrade of High Resolution Mass Spectrometers consists of assembling high-end commercial instrumentation from reputable manufacturers with a minimal amount of customization to replace the electronics for the older systems. By taking advantage of advances in instrumentation, precise magnet control can be achieved using high resolution current sources and continuous feedback from a high resolution hall-effect probe. The custom equipment include a precision voltage divider/summing amplifier chassis, high voltage power supply chassis and a chassis for controlling the voltage emission for the mass spectrometer source tube. The upgrade package is versatile enough to interface with valve control, vacuum and other instrumentation. Instrument communication is via a combination of Ethernet and traditional IEEE-488 GPIB protocols. The system software upgrades include precision control, feedback and spectral waveform analysis tools.

  14. Laser resonance ionization mass spectrometer

    The setup is elaborated for the trace detection of transuranium elements by the three-step laser resonance ionization combined with the time-of-flight mass spectrometry. The setup efficiency for detection of plutonium was measured to be about 0.5 centre dot 10-8 ion/atom, and its selectivity relative to atoms of another elements has the order of 1013 atom/atom

  15. Small system for tritium accelerator mass spectrometry

    Roberts, Mark L.; Davis, Jay C.

    1993-01-01

    Apparatus for ionizing and accelerating a sample containing isotopes of hydrogen and detecting the ratios of hydrogen isotopes contained in the sample is disclosed. An ion source generates a substantially linear ion beam including ions of tritium from the sample. A radio-frequency quadrupole accelerator is directly coupled to and axially aligned with the source at an angle of substantially zero degrees. The accelerator accelerates species of the sample having different mass to different energy levels along the same axis as the ion beam. A spectrometer is used to detect the concentration of tritium ions in the sample. In one form of the invention, an energy loss spectrometer is used which includes a foil to block the passage of hydrogen, deuterium and .sup.3 He ions, and a surface barrier or scintillation detector to detect the concentration of tritium ions. In another form of the invention, a combined momentum/energy loss spectrometer is used which includes a magnet to separate the ion beams, with Faraday cups to measure the hydrogen and deuterium and a surface barrier or scintillation detector for the tritium ions.

  16. High-precision accelerator-mass-spectrometer radiocarbon dating of buried tidal-marsh soils - An approach to estimating the frequency and coastal extent of subduction zone earthquakes in Oregon and Washington

    Accurate and precise radiocarbon dating of buried tidal-marsh soils in estuarine stratigraphic sequences in the Pacific Northwest can help distinguish soils submerged during regional plate-boundary earthquakes from soils submerged during local upper-plate earthquakes or by non-tectonic processes. More precise ages than those resulting from conventional methods of radiocarbon analysis can be obtained by averaging multiple accelerator-mass-spectrometer (AMS) 14C ages of rigorously selected and pretreated plant macrofossils at the abrupt upper contacts of tidal-marsh soils. An initial test of this method in Coos Bay, Oregon, shows that standard deviations on AMS ages can be reduced to ± 25-40 radiocarbon years. But consideration of the total analytical errors in AMS analysis and age differences due to variations in the rate of 14C production in the atmosphere over time indicate that 95% confidence limits on calendar-corrected ages for submergence events range from 50 to 450 years

  17. 21 CFR 862.2860 - Mass spectrometer for clinical use.

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Mass spectrometer for clinical use. 862.2860... Instruments § 862.2860 Mass spectrometer for clinical use. (a) Identification. A mass spectrometer for... by means of an electrical and magnetic field according to their mass. (b) Classification. Class...

  18. Automation of a thermal ionisation mass spectrometer

    A thermal ionization mass spectrometer was upgraded in order to be monitored by a PC. A PC-LMP-16 National Instruments data acquisition board was used for the ion current channel and the Hall signal channel. A dedicated interface was built to allow commands from the computer to the current supply of the analyzing magnet and to the high voltage unit of the mass spectrometer. A software application was worked out to perform the adjustment of the spectrometer, magnetic scanning and mass spectra acquisition, data processing and isotope ratio determination. The apparatus is used for isotope ratio 235 U/238 U determination near the natural abundance. A peak jumping technique is applied to choose between the 235 U and 238 U signal, by switching the high voltage applied to the ion source between two preset values. This avoids the delay between the acquisition of the peaks of interest, a delay that would appear in the case of a 'pure' magnetic scanning. Corrections are applied for the mass discrimination effects and a statistical treatment of the data is achieved. (authors)

  19. Measuring transfer of 14C-PCB from maternal diet to milk in a goat model using an accelerator mass spectrometer (AMS)

    Environmental pollutants pose a substantial risk to nursing infants. Many of these toxicants (i.e. PCBs, PBDEs, mercury) are passed from the maternal diet to the nursing infant in breast milk. Determining the toxicokinetics has been difficult to measure due to ethical limitations. Since extremely small amounts of 14C can be measured using Accelerator Mass Spectrometry (AMS), a goat model was used to establish a minimum oral dose of 14C-labeled PCB (2,2',4,4',5,5'-hexachlorobiphenyl-UL-14C) that could be given to a lactating animal and traced into the milk. An oral dose of 66 nCi/kg body weight (1.84 μg PCB/kg bw) was administered. Plasma and milk samples were collected for 2 months after dosing. The concentration of 14C label reached a peak value of 1.71 ng/ml PCB equivalents in the milk on day 2 and then declined to about 135 pg/ml PCB equivalents in the milk at 3 weeks. A second goat was administered a smaller dose (22 nCi/kg bw; 616 ng PCB/kg bw). A peak concentration of 485 pg PCB equivalents/ml milk occurred at 3 days and declined to 77.6 pg PCB equivalents/ml milk by 3 weeks. Our results indicated that an even lower dosage of labeled-PCB could be used due to the extreme sensitivity of AMS measurement. Extrapolating from current data it is estimated that the dose could be reduced by a factor of 20 (31 ng PCB/kg bw; 1.1 nCi/kg bw) and still be detectable after 2 months. Thus, the potential exists for developing protocols for studying toxicokinetics in humans using radiologically- and toxicologically-benign doses of labeled environmental toxicants

  20. Accelerator mass spectrometry: state of the art

    Tuniz, C. [Australian Nuclear Science and Technology Organisation, Lucas Heights, NSW (Australia)

    1996-12-31

    Accelerator Mass Spectrometry (AMS) is the analytical technique of choice for the detection of long-lived radionuclides which cannot be practically analysed with decay counting or conventional mass spectrometry. The main use of AMS has been in the analysis of radiocarbon and other cosmogenic radionuclides for archaeological, geological and environmental applications. In addition, AMS has been recently applied in biomedicine to study exposure of human tissues to chemicals and biomolecules at attomole levels. There is also a world-wide effort to analyse rare nuclides of heavier masses, such as long-lived actinides, with important applications in safeguards and nuclear waste disposal. The use of AMS is limited by the expensive accelerator technology required and there are several attempts to develop smaller and cheaper AMS spectrometers. 5 refs.

  1. Effective mass spectrometer. [History and accomplishments

    Ayres, D.

    1979-10-12

    The history and major accomplishments of the Effective Mass Spectrometer (EMS) are described. In the eight years since the EMS turned on, 21 experiments have been completed by groups from nine institutions in 32 months of operation. Over 400 million triggers have been recorded on magnetic tape, resulting in 29 journal publications to date. A list of experimental proposals for the EMS and a sampling of results are presented. 12 figures, 4 tables.

  2. Double focussing stigmatic image mass spectrometer

    The mass spectrometer for the analysis of ions, which occur in matetial pulverisation by a radiation micro probe, contains one lens a 450 spherical condenser lens, from which the ion beam emerhes as a parallel beam, an intermediate shutter, a 900 magnetic field and an outlet shutter. The angle of entry and energy bandwidth can be set independently of each other. An optimum transmission is obtained with the least possible image errors. (DG)

  3. Mass spectrometer for the analyses of gases

    A 6-in-radius, 600 magnetic-sector mass spectrometer (designated as the MS-200) has been constructed for the quantitative and qualitative analyses of fixed gases and volatile organics in the concentration range from 1 ppM (by volume) to 100%. A partial pressure of 1 x 10-6 torr in the inlet expansion volume is required to achieve a useful signal at an electron-multiplier gain of 10,000

  4. Progress with the PENTATRAP mass spectrometer

    Bekker, Hendrik; Crespo Lopez-Urrutia, Jose; Doerr, Andreas; Eliseev, Sergey; Goncharov, Mikhail; Repp, Julia; Rischka, Alexander; Roux, Christian; Sturm, Sven; Blaum, Klaus [Max-Planck-Institut fuer Kernphysik, 69117 Heidelberg (Germany); Boehm, Christine [Max-Planck-Institut fuer Kernphysik, 69117 Heidelberg (Germany); ExtreMe Matter Institute EMMI, Helmholtz Gemeinschaft, 64291 Darmstadt (Germany); Novikov, Yuri [PNPI, Gatchina, 188300 St. Petersburg (Russian Federation)

    2014-07-01

    The five-trap mass spectrometer PENTATRAP has been constructed and is currently being characterized at the Max-Planck-Institut fuer Kernphysik, Heidelberg. It aims for high-precision mass ratio measurements with a relative mass uncertainty of a few 10{sup -12}. Long-lived and stable, highly charged nuclides with masses up to uranium will be addressed to perform e.g. stringent tests of quantum electrodynamics and neutrino oriented mass measurements. The main part of the experiment is a stack of five cylindrical cryogenic Penning traps. An ultra-stable voltage source is required to supply the Penning trap electrodes with appropriate and stable potentials. Therefore, an elaborated source was developed and built at MPIK. Recently, first ions have been successfully trapped. Details about the progress of the installation, especially the status of the voltage source and first ion signals are presented in the talk.

  5. Differentially pumped dual linear quadrupole ion trap mass spectrometer

    Owen, Benjamin C.; Kenttamaa, Hilkka I.

    2015-10-20

    The present disclosure provides a new tandem mass spectrometer and methods of using the same for analyzing charged particles. The differentially pumped dual linear quadrupole ion trap mass spectrometer of the present disclose includes a combination of two linear quadrupole (LQIT) mass spectrometers with differentially pumped vacuum chambers.

  6. Recent exploits of the ISOLTRAP mass spectrometer

    Highlights: • Update on ISOLTRAP. • Reference carbon clusters for heavy species. • Ion-beam yield analysis with MR-TOF MS. Q -- Abstract: The Penning-trap mass spectrometer ISOLTRAP, located at the isotope-separator facility ISOLDE (CERN), is presented in its current form taking into account technical developments since 2007. Three areas of developments are presented. The reference ion sources have been modified to guarantee a sufficient supply of reference ions for mass measurements and systematic studies. Different excitation schemes have been investigated for manipulation of the ion motion in the Penning trap, to enhance either the purification or measurement process. A multi-reflection time-of-flight mass separator has been implemented and can now be routinely used for purification and as a versatile tool for beam analysis

  7. Recent exploits of the ISOLTRAP mass spectrometer

    Kreim, S; Naimi, S; Blaum, K; Breitenfeldt, M; Rossel, R E; Fink, D; Stanja, J; Atanasov, D; Borgmann, Ch; Cocolios, T E; Zuber, K; Wolf, R N; George, S; Neidherr, D; Nicol, T; Rosenbusch, M; Lunney, D; Boehm, Ch; Manea, V; Herlert, A; Koester, U; Beck, D; Wienholtz, F; Kellerbauer, A; Ramirez, E Minaya; Schweikhard, L

    2013-01-01

    The Penning-trap mass spectrometer ISOLTRAP, located at the isotope-separator facility ISOLDE (CERN), is presented in its current form taking into account technical developments since 2007. Three areas of developments are presented. The reference ion sources have been modified to guarantee a sufficient supply of reference ions for mass measurements and systematic studies. Different excitation schemes have been investigated for manipulation of the ion motion in the Penning trap, to enhance either the purification or measurement process. A multi-reflection time-of-flight mass separator has been implemented and can now be routinely used for purification and as a versatile tool for beam analysis. (C) 2013 Elsevier B.V. All rights reserved.

  8. Symposium on accelerator mass spectrometry

    None

    1981-01-01

    The area of accelerator mass spectrometry has expanded considerably over the past few years and established itself as an independent and interdisciplinary research field. Three years have passed since the first meeting was held at Rochester. A Symposium on Accelerator Mass Spectrometry was held at Argonne on May 11-13, 1981. In attendance were 96 scientists of whom 26 were from outside the United States. The present proceedings document the program and excitement of the field. Papers are arranged according to the original program. A few papers not presented at the meeting have been added to complete the information on the status of accelerator mass spectrometry. Individual papers were prepared separately for the data base.

  9. Symposium on accelerator mass spectrometry

    The area of accelerator mass spectrometry has expanded considerably over the past few years and established itself as an independent and interdisciplinary research field. Three years have passed since the first meeting was held at Rochester. A Symposium on Accelerator Mass Spectrometry was held at Argonne on May 11-13, 1981. In attendance were 96 scientists of whom 26 were from outside the United States. The present proceedings document the program and excitement of the field. Papers are arranged according to the original program. A few papers not presented at the meeting have been added to complete the information on the status of accelerator mass spectrometry. Individual papers were prepared separately for the data base

  10. MEMS mass spectrometers: the next wave of miniaturization

    Syms, Richard R. A.; Wright, Steven

    2016-02-01

    This paper reviews mass spectrometers based on micro-electro-mechanical systems (MEMS) technology. The MEMS approach to integration is first briefly described, and the difficulties of miniaturizing mass spectrometers are outlined. MEMS components for ionization and mass filtering are then reviewed, together with additional components for ion detection, vacuum pressure measurement and pumping. Mass spectrometer systems containing MEMS sub-components are then described, applications for miniaturized and portable systems are discussed, and challenges and opportunities are presented.

  11. MEMS mass spectrometers: the next wave of miniaturization

    This paper reviews mass spectrometers based on micro-electro-mechanical systems (MEMS) technology. The MEMS approach to integration is first briefly described, and the difficulties of miniaturizing mass spectrometers are outlined. MEMS components for ionization and mass filtering are then reviewed, together with additional components for ion detection, vacuum pressure measurement and pumping. Mass spectrometer systems containing MEMS sub-components are then described, applications for miniaturized and portable systems are discussed, and challenges and opportunities are presented. (topical review)

  12. Resolution of time-of-flight mass spectrometers evaluated for secondary neutral mass spectrometry

    Kato, Makoto; Mogami, Akinori; Naito, Motohiro; Ichimura, Shingo; Shimizu, Hazime

    1988-09-01

    Mass resolution of a time-of-flight mass spectrometer with a two-stage electrostatic reflector is calculated for secondary neutral mass spectrometry. The instrument parameters are optimized for energy and space focusing: correcting the flight time difference due to the energy width ΔE of sputtered particles and the spatial width Δs of an ionizing laser beam. The effect of Δs can be compensated by applying an acceleration field to the ionizing region, and the maximum resolution becomes about 1000 for ΔE=10 eV and Δs=1.0 mm.

  13. Zinc isotope discrimination effect in inductively coupled plasma mass spectrometer

    Inductively coupled plasma mass spectrometry (ICPMS) has recently been used for isotope ratio analysis. The isotope discrimination effect in the mass spectrometer is a primary factor contributing to loss of precision and accuracy in isotope ratio analysis. The discrimination effect of zinc isotopes was investigated by comparing the results obtained using a quadrupole type ICPMS with those obtained using a thermal ionization mass spectrometer

  14. Passive neutron dosemeter-spectrometer for high-energy accelerators

    A passive neutron dosemeter-spectrometer (PNDS) with fission fragments converters is described. The results obtained show that it is a convenient and reliable instrument for neutron dose equivalent measurement in the calibration performing and response investigations of personnel dosemeters in mixed radiation fields behind accelerator shielding. Because of the possibility of neutron spectrum estimation in a wide energy range PNDS using is promissing in the neutron radiation fields research and also as an accidental neutron dosemeter. 23 refs.; 10 figs.; 4 tabs

  15. Analysis of corrosive materials on GD-150 mass spectrometer

    A study has been made to extend the use of Varian Mat GD-150 mass/spectrometer for the corrosive gas analysis. Chlorine, bromine and thiophosgene have been used for this purpose. The feasibility studies, calibration of mass spectrometer and the measuring techniques have been discussed for the aforesaid analysis. (author)

  16. Estimation of the Beam Width in Magnetic Mass Spectrometer

    O.N. Peregudov

    2010-01-01

    Full Text Available A method for estimation of the beam width in magnetic sector mass spectrometers is proposed. This method consists in the restoration of the initial ion density distribution function in a beam cross-section before the receiving collector slit and can be used for the qualitative estimation of the mass spectrometer ion-optical scheme.

  17. Accelerator mass spectrometry programme at Mumbai pelletron accelerator facility

    The Accelerator Mass Spectrometry (AMS) programme and the related developments based on the Mumbai Pelletron accelerator are described. The initial results of the measurement of the ratio, 36Cl / Cl in water samples are presented. (author)

  18. Neuroscience and Accelerator Mass Spectrometry

    Palmblad, M N; Buchholz, B A; Hillegonds, D J; Vogel, J S

    2004-08-02

    Accelerator mass spectrometry (AMS) is a mass spectrometric method for quantifying rare isotopes. It has had great impact in geochronology and archaeology and is now being applied in biomedicine. AMS measures radioisotopes such as {sup 3}H, {sup 14}C, {sup 26}Al, {sup 36}Cl and {sup 41}Ca, with zepto- or attomole sensitivity and high precision and throughput, enabling safe human pharmacokinetic studies involving: microgram doses, agents having low bioavailability, or toxicology studies where administered doses must be kept low (<1 {micro}g/kg). It is used to study long-term pharmacokinetics, to identify biomolecular interactions, to determine chronic and low-dose effects or molecular targets of neurotoxic substances, to quantify transport across the blood-brain barrier and to resolve molecular turnover rates in the human brain on the timescale of decades. We will here review how AMS is applied in neurotoxicology and neuroscience.

  19. Mass spectrometer experiments for the European space probe Giotto

    Neumann, G.

    The Particulate Impact Analyzer (PIA) and Neutral Mass Spectrometer (NMS) experiments to be carried on board the Giotto cometary probe are presented. The NMS is designed to determine the chemical composition of gases and ions in the coma of Halley's Comet based on the ue of two spectrometers: an electrostatic parallel-plate analyzer, and a similar analyzer coupled with a magnetic analyzer with double-focusing geometry. The sensor structure consists of a monolithic multi-rib milled body with integral fixation points, with provisions for electromagnetic and thermal isolation, and dust protection. The PIA is intended for the measurement of the physical and chemical characteristics of cometary dust particles. It is based on an instrument comprising an entrance baffle and shutter unit, a target unit at which the dust is ionized, a light flash detector marking the flash of ionization, an acceleration grid sending the ions into the time-of-flight unit, and a multiplier unit for recording the time of flight spectrum. A microprocessor-based electronics system housed in a separate case next to the sensor performs tasks of power supply, signal processing, data processing and flow control.

  20. Multiple-ion-beam time-of-flight mass spectrometer

    An innovative approach to increase the throughput of mass spectrometric analyses using a multiple-ion-beam mass spectrometer is described. Two sample spots were applied onto a laser desorption/ionization target and each spot was simultaneously irradiated by a beam of quadrupled Nd:YLF laser radiation (261.75 nm) to produce ions by laser-desorption ionization. Acceleration of the ions in an electric field created parallel ion beams that were focused by two parallel einzel lens systems. After a flight path of 2.34 m, the ions were detected with a microchannel plate-phosphor screen assembly coupled with a charge coupled device camera that showed two resolved ion beams. Time-of-flight mass spectra were also obtained with this detector. Experiments were performed using both metal atom cations (Ti+ and Cr+) produced by laser desorption/ionization and the molecular ions of two different proteins (myoglobin and lysozyme), created by matrix assisted laser desorption/ionization using an excess of nicotinic acid as matrix

  1. Miniature Mass Spectrometer for Earth Science Research Project

    National Aeronautics and Space Administration — By drastically reducing the physical footprint of a mass spectrometer to the size of a beverage can, Ceramitron could set a new performance/price standard in the...

  2. Quadrupole Time-of-Flight Mass Spectrometer

    Federal Laboratory Consortium — FUNCTION: The system generates superior quality mass spectrometry (MS) and tandem mass spectrometry (MS/MS) data from both atmospheric pressure ionization (API) and...

  3. Mass spectrometers based on a cone-shaped acromatic prism

    We have elaborated a mass spectrometer without lenses consisting of one conic achromatic prism. It has a specific mass dispersion which is equal to 67.5 mm/m per 1% change of mass. (By specific dispersion we mean linear dispersion related to the main path.) The pass of charged particles with different emittance is investigated with the help of integrating precise equations for tracks of charged particles in natural curvilinear coordinates. We have calculated the resolving power and aberration of a mass spectrometer for different beams of particles. It is evident that the mass spectrometer is particularly effective in use when we deal with rather wide ion beams having an insignificant angular divergence in the mean plane. (orig.)

  4. Mass spectrometers based on a cone-shaped acromatic prism

    Spivak-Lavrov, I.F. [Pedagogical Inst. of Aktyubinsk (Kazakhstan)

    1995-09-01

    We have elaborated a mass spectrometer without lenses consisting of one conic achromatic prism. It has a specific mass dispersion which is equal to 67.5 mm/m per 1% change of mass. (By specific dispersion we mean linear dispersion related to the main path.) The pass of charged particles with different emittance is investigated with the help of integrating precise equations for tracks of charged particles in natural curvilinear coordinates. We have calculated the resolving power and aberration of a mass spectrometer for different beams of particles. It is evident that the mass spectrometer is particularly effective in use when we deal with rather wide ion beams having an insignificant angular divergence in the mean plane. (orig.).

  5. Real time spectrometer for thermal neutrons from radiotherapic accelerators

    Mozzanica, A. [Universita degli Studi di Brescia e INFN sezione di Pavia (Italy)], E-mail: mozzanica@bs.infn.it; Bartesaghi, G.; Bolognini, D.; Conti, V.; Mascagna, V.; Prest, M.; Scazzi, S. [Universita degli Studi dell' Insubria e INFN sezione di Milano/Milano Bicocca (Italy); Cappelletti, P.; Frigerio, M.; Gelosa, S.; Monti, A.; Ostinelli, A. [Fisica Sanitaria, Ospedale S. Anna di Como (Italy); Bevilacqua, R.; Giannini, G.; Totaro, P.; Vallazza, E. [INFN, sezione di Trieste e Universita degli Studi di Trieste (Italy)

    2007-10-15

    Radiotherapy accelerators can produce high energy photon beams for deep tumour treatments. Photons with energies greater than 8 MeV produce neutrons via photoproduction. The PHONES (PHOto NEutron Source) project is developing a neutron moderator to use the photoproduced neutrons for BNCT (Boron Neutron Capture Therapy) in hospital environments. In this framework we are developing a real time spectrometer for thermal neutrons exploiting the bunch structure of the beam. Since the beam is produced by a linear accelerator, in fact, particles are sent to the patient in bunches with a rate of 150-300 Hz depending on the beam type and energy. The neutron spectrum is usually measured with integrating detectors such as bubble dosimeters or TLDs, which integrate over a time interval and an energy one. We are developing a scintillator detector to measure the neutron spectrum in real time in the interval between bunches, that is in the thermal region. The signals from the scintillator are discriminated and sampled by a dedicated clock in a Cyclone II FPGA by Altera, thus obtaining the neutron time of flight spectrum. The exploited physical process in ordinary plastic scintillators is neutron capture by H with a subsequent {gamma} emission. The measured TOF spectrum has been compared with a BF{sub 3} counter one. A dedicated simulation with MCNP is being developed to extract the energy spectrum from the TOF one. The paper will present the results of the prototype measurements and the status of the simulation.

  6. Design of the multi-reflection time-of-flight mass spectrometer for the RAON facility

    Yoon J. W.

    2014-03-01

    Full Text Available Electrodes design for the multi-reflection time-of-flight mass spectrometer (MR-TOF-MS has been performed for the high precision mass measurement system in RAON accelerator facility, which will be constructed in Korea. Calculated mass resolution is 105 for the condition of an energy spread of ± 30 eV and an emittance of 0.75 π mm mrad. MR-TOF-MS will be used for the isobar separation and the mass measurement for very short-lived isotopes.

  7. Development of an ion mobility spectrometer for use in an atmospheric pressure ionization ion mobility spectrometer/mass spectrometer instrument for fast screening analysis

    Sysoev, A; Adamov, A; Vildanoja, J; Ketoja, RA; Kostiainen, R; Kotiaho, T

    2004-01-01

    An ion mobility spectrometer that can easily be installed as an intermediate component between a commercial triple-quadrupole mass spectrometer and its original atmospheric pressure ionization (API) sources was developed. The curtain gas from the mass spectrometer is also used as the ion mobility sp

  8. Glow discharge electron impact ionization source for miniature mass spectrometers.

    Gao, Liang; Song, Qingyu; Noll, Robert J; Duncan, Jason; Cooks, R Graham; Ouyang, Zheng

    2007-05-01

    A glow discharge electron impact ionization (GDEI) source was developed for operation using air as the support gas. An alternative to the use of thermoemission from a resistively heated filament electron source for miniature mass spectrometers, the GDEI source is shown to have advantages of long lifetime under high-pressure operation and low power consumption. The GDEI source was characterized using our laboratory's handheld mass spectrometer, the Mini 10. The effects of the discharge voltage and pressure were investigated. Design considerations are illustrated with calculations. Performance is demonstrated in a set of experimental tests. The results show that the low power requirements, mechanical ruggedness, and quality of the data produced using the small glow discharge ion source make it well-suited for use with a portable handheld mass spectrometer. PMID:17441220

  9. Double focusing mass spectrometers of second order

    The resolution of the on-line mass spectrograph is normally several hundred and this is sufficient to separate nuclei having different mass number A. If the nuclei to be analyzed have the same A but different charge number Z, they can not be separated by this amount of resolution. However, the complete separation of nuclei (both A and Z) can be possible if the resolution is raised by about hundred times, that is, up to several ten thousands. The resolving power of about 30,000 would be sufficient to resolve all nuclei far from the valley of beta-stability. Besides, the direct mass measurement of short lived nuclei would be possible with such a high resolution mass spectrograph. The determination of masses of nuclei far from beta-stability is also a very interesting and important problem. For this purpose, a mass spectrograph which can collect many ions and still has a high resolution is necessary. In order to satisfy such conditions, it is essentially necessary to realize good focusing. Therefore, the possibility of correcting for second order image aberrations of a double focusing instrument is investigated and several suitable designs are found by computer calculation

  10. Shotgun lipidomics on a LTQ Orbitrap mass spectrometer by successive switching between acquisition polarity modes

    Schuhmann, K.; Almeida, R.; Baumert, M.;

    2012-01-01

    accuracy. Here, we report on a method to rapidly acquire high-resolution spectra in both polarity modes with sub-ppm mass accuracy and demonstrate that it not only simplifies and accelerates shotgun lipidomics analyses but also improves the lipidome coverage because more lipid classes and more individual......Topdown shotgun lipidomics relies on direct infusion of total lipid extracts into a high-resolution tandem mass spectrometer and implies that individual lipids are recognized by their accurately determined m/z. Lipid ionization efficiency and detection specificity strongly depend on the acquisition...... polarity, and therefore it is beneficial to analyze lipid mixtures in both positive and negative modes. Hybrid LTQ Orbitrap mass spectrometers are widely applied in topdown lipidomics; however, rapid polarity switching was previously unfeasible because of the severe and immediate degradation of mass...

  11. Cherenkov detectors and a new effective-mass spectrometer method

    Hladký, Jan

    2006-01-01

    Roč. 75, - (2006), s. 854-855. ISSN 0969-806X Institutional research plan: CEZ:AV0Z10100502 Keywords : Cherenkov radiation * spectrometer * effective mass method Subject RIV: BF - Elementary Particles and High Energy Physics Impact factor: 0.868, year: 2006

  12. Enrichment of rare isotopes using a quadrupole mass spectrometer

    A small quadrupole mass spectrometer was operated in the static mode to enrich selected rare gas isotopes. Memory effects in the apparatus were observed and attributed to the re-emission of atoms implanted by the electron-impact ion source. Studies of the pumping mechanism led to a practical means for reducing the rate of noble gas pumping. (author)

  13. SMAD-2A mass spectrometer core isotopic analysis of water

    SMAT-2A is a small mass spectrometer for water isotopes analysis, double collector method (HD/H2 ratio). Improvements in maintenance automation data acquisition and processing are presented. Analyses of liquid and gaseous samples were made and internal reproducibility and precision are calculated. (Author)

  14. The History of Planetary Exploration Using Mass Spectrometers

    Mahaffy, Paul R.

    2012-01-01

    At the Planetary Probe Workshop Dr. Paul Mahaffy will give a tutorial on the history of planetary exploration using mass spectrometers. He will give an introduction to the problems and solutions that arise in making in situ measurements at planetary targets using this instrument class.

  15. Micro mass spectrometer on a chip.

    Cruz, Dolores Y.; Blain, Matthew Glenn; Fleming, James Grant

    2005-11-01

    The design, simulation, fabrication, packaging, electrical characterization and testing analysis of a microfabricated a cylindrical ion trap ({mu}CIT) array is presented. Several versions of microfabricated cylindrical ion traps were designed and fabricated. The final design of the individual trap array element consisted of two end cap electrodes, one ring electrode, and a detector plate, fabricated in seven tungsten metal layers by molding tungsten around silicon dioxide (SiO{sub 2}) features. Each layer of tungsten is then polished back in damascene fashion. The SiO{sub 2} was removed using a standard release processes to realize a free-hung structure. Five different sized traps were fabricated with inner radii of 1, 1.5, 2, 5 and 10 {micro}m and heights ranging from 3-24 {micro}m. Simulations examined the effects of ion and neutral temperature, the pressure and nature of cooling gas, ion mass, trap voltage and frequency, space-charge, fabrication defects, and other parameters on the ability of micrometer-sized traps to store ions. The electrical characteristics of the ion trap arrays were determined. The capacitance was 2-500 pF for the various sized traps and arrays. The resistance was in the order of 1-2 {Omega}. The inductance of the arrays was calculated to be 10-1500 pH, depending on the trap and array sizes. The ion traps' field emission characteristics were assessed. It was determined that the traps could be operated up to 125 V while maintaining field emission currents below 1 x 10{sup -15} A. The testing focused on using the 5-{micro}m CITs to trap toluene (C{sub 7}H{sub 8}). Ion ejection from the traps was induced by termination of the RF voltage applied to the ring electrode and current measured on the collector electrode suggested trapping of ions in 1-10% of the traps. Improvements to the to the design of the traps were defined to minimize voltage drop to the substrate, thereby increasing trapping voltage applied to the ring electrode, and to

  16. A microelectromechanical systems-enabled, miniature triple quadrupole mass spectrometer.

    Wright, Steven; Malcolm, Andrew; Wright, Christopher; O'Prey, Shane; Crichton, Edward; Dash, Neil; Moseley, Richard W; Zaczek, Wojciech; Edwards, Peter; Fussell, Richard J; Syms, Richard R A

    2015-03-17

    Miniaturized mass spectrometers are becoming increasingly capable, enabling the development of many novel field and laboratory applications. However, to date, triple quadrupole tandem mass spectrometers, the workhorses of quantitative analysis, have not been significantly reduced in size. Here, the basis of a field-deployable triple quadrupole is described. The key development is a highly miniaturized ion optical assembly in which a sequence of six microengineered components is employed to generate ions at atmospheric pressure, provide a vacuum interface, effect ion guiding, and perform fragmentation and mass analysis. Despite its small dimensions, the collision cell efficiently fragments precursor ions and yields product ion spectra that are very similar to those recorded using conventional instruments. The miniature triple quadrupole has been used to detect thiabendazole, a common pesticide, in apples at a level of 10 ng/g. PMID:25708099

  17. Laser Proton acceleration from mass limited silicon foils

    Zeil, K.; Kraft, S.; Richter, T.; Metzkes, J.; Bussmann, M.; Schramm, U.; Sauerbrey, R.; Cowan, T. E.; Fuchs, J.; Buffechoux, S.

    2009-11-01

    We present recent studies on laser proton acceleration experiments using mass limited silicon targets. Small micro machined silicon foils with 2 μm thickness and 20x20 μm2 to 100x100μm2 size mounted on very tiny stalks were shot with the 100 TW LULI Laser (long pulse 150 fs) and with the new 150 TW DRACO Laser facility (short pulse 30 fs) of the Research Centre Dresden-Rossendorf. The experiments were carried out using high contrast levels. Proton spectra have been measured with magnetic spectrometers and radio chromic film stacks.

  18. Interface for the rapid analysis of liquid samples by accelerator mass spectrometry

    Turteltaub, Kenneth; Ognibene, Ted; Thomas, Avi; Daley, Paul F; Salazar Quintero, Gary A; Bench, Graham

    2014-02-04

    An interface for the analysis of liquid sample having carbon content by an accelerator mass spectrometer including a wire, defects on the wire, a system for moving the wire, a droplet maker for producing droplets of the liquid sample and placing the droplets of the liquid sample on the wire in the defects, a system that converts the carbon content of the droplets of the liquid sample to carbon dioxide gas in a helium stream, and a gas-accepting ion source connected to the accelerator mass spectrometer that receives the carbon dioxide gas of the sample in a helium stream and introduces the carbon dioxide gas of the sample into the accelerator mass spectrometer.

  19. Preliminary results from LADEE's Neutral Mass Spectrometer (NMS)

    Benna, Mehdi; Mahaffy, Paul; Hodges, Richard

    2014-05-01

    The Neutral Mass Spectrometer (NMS) of the Lunar Atmosphere and Dust Environment Explorer (LADEE) Mission is a high sensitivity quadrupole mass spectrometer designed to measure the composition and variability of the tenuous lunar atmosphere. The instrument has been observing the lunar exosphere since 10/17/2013, initially from a near circular 250 km altitude orbit and since 11/11/2013 from an elliptical orbit that reaches to 30-60 km altitude near the sunrise terminator. During its first four months in orbit, the NMS instrument successfully detected exospheric helium, argon and neon and mapped their spatial and temporal variability. Furthermore, the NMS instrument was able to establish new upper limits for many other exospheric species either sputtered or thermally evolved from the lunar surface. This talk will summarize these preliminary results from the NMS measurements.

  20. A new computerized mass spectrometer for isotopic analyses of solids

    VARIAN MAT's new MAT 260 mass spectrometer system which is intended for automatic precision analysis of isotope ratios in solids (U, Pu, Rb, Sr, Pb and others) is described. The MAT 260 features exceptional performance for exceeding previous standards. The programmable desk calculator and the exceptionally sensitive ion source which contribute to the excellent standard of the system are discussed. The specifications and the applications to which the system can be put are also discussed. (K.B.)

  1. Commissioning of the AEI MS702 mass spectrometer

    The setting-up and commissioning of the AEI MS702 mass spectrometer is described. Its individual components and their use are discussed, as well as the sample preparation, analysis, and reduction of data. A comprehensive list is given of instrumental breakdowns, and the application of the technique to several matrices is outlined. Improvements and modifications to the technique, including the use of a minicomputer, are suggested

  2. Determining gaseous composition of fluid inclusions with quadrupole mass spectrometer

    朱和平; 王莉娟

    2002-01-01

    Quadrupole mass spectrometer (QMS) is an instrument for effectively determining gaseous composition of fluid inclusion. The gaseous component is extracted from inclusions with thermal decrepitation method and then determined with the sensitive QMS instrument. The method is characterized by high sensitivity and high accuracy with the relative standard deviation (RSD, n = 6) of less than 3%. It has been successfully used for analyzing fluid inclusions. The analytical re-sults meet the requirement of geological study.

  3. A high efficiency thermal ionization source adapted to mass spectrometers

    A tungsten crucible thermal ionization source mounted on a quadrupole mass spectrometer is described. The crucible is a disposable rod with a fine hole bored in one end; it is heated by electron bombardment. The schematic design of the assembly, including water cooling, is described and depicted. Historically, the design is derived from that of ion sources used on ion separators at Los Alamos and Dubna, but the crucible is made smaller and simplified. 10 refs., 4 figs

  4. Method development of gas analysis with mass spectrometer

    Dissolved gas content in deep saline groundwater is an important factor, which has to be known and taken into account when planning the deep repository for the spent nuclear fuel. Posiva has investigated dissolved gases in deep groundwaters since the 1990's. In 2002 Posiva started a project that focused on developing the mass spectrometric method for measuring the dissolved gas content in deep saline groundwater. The main idea of the project was to analyse the dissolved gas content of both the gas phase and the water phase by a mass spectrometer. The development of the method started in 2003 (in the autumn). One of the aims was to create a parallel method for gas analysis with the gas chromatographic method. The starting point of this project was to test if gases could be analysed directly from water using a membrane inlet in the mass spectrometer. The main objective was to develop mass spectrometric methods for gas analysis with direct and membrane inlets. An analysis method for dissolved gases was developed for direct gas inlet mass spectrometry. The accuracy of the analysis method is tested with parallel real PAVE samples analysed in the laboratory of Insinoeoeritoimisto Paavo Ristola Oy. The results were good. The development of the membrane inlet mass spectrometric method still continues. Two different membrane materials (silicone and teflon) were tested. Some basic tests (linearity,repeatability and detection limits for different gases) will be done by this method. (orig.)

  5. Augmenting Ion Trap Mass Spectrometers Using a Frequency Modulated Drift Tube Ion Mobility Spectrometer.

    Morrison, Kelsey A; Siems, William F; Clowers, Brian H

    2016-03-15

    Historically, high pressure ion mobility drift tubes have suffered from low ion duty cycles and this problem is magnified when such instrumentation is coupled with ion trap mass spectrometers. To significantly alleviate these issues, we outline the result from coupling an atmospheric pressure, dual-gate drift tube ion mobility spectrometer (IMS) to a linear ion trap mass spectrometer (LIT-MS) via modulation of the ion beam with a linear frequency chirp. The time-domain ion current, once Fourier transformed, reveals a standard ion mobility drift spectrum that corresponds to the standard mode of mobility analysis. By multiplexing the ion beam, it is possible to successfully obtain drift time spectra for an assortment of simple peptide and protein mixtures using an LIT-MS while showing improved signal intensity versus the more common signal averaging technique. Explored here are the effects of maximum injection time, solution concentration, total experiment time, and frequency swept on signal-to-noise ratios (SNRs) and resolving power. Increased inject time, concentration, and experiment time all generally led to an improvement in SNR, while a greater frequency swept increases the resolving power at the expense of SNR. Overall, chirp multiplexing of a dual-gate IMS system coupled to an LIT-MS improves ion transmission, lowers analyte detection limits, and improves spectral quality. PMID:26854901

  6. Weighing excited nuclear states with a Penning trap mass spectrometer

    We report on high-accuracy mass measurements and isomer identification of 187Pb. In this nuclide, two close-lying isomeric states are known from α-decay studies. With the combined use of the ISOLDE resonance ionization laser ion source and the Penning trap mass spectrometer ISOLTRAP the energy difference of 187Pb and 187mPb was determined to be E = 33(13) keV. This is the lowest isomeric excitation energy ever determined by weighing nuclei. (orig.)

  7. Accelerator mass spectrometry programme at BARC-TIFR pelletron accelerator

    Accelerator based mass spectrometry (ABMs) is an ultra sensitive means of counting individual atoms having sufficiently long half life and available in small amount. The 14 U D Pelletron Accelerator is an ideal machine to carry out ABMs studies with heavy isotopes like 36Cl and 129I. Cosmogenic radio isotope 36Cl is widely being detected using ABMs as it has got applications in ground water research, radioactive waste management, atmospheric 36Cl transport mechanism studies of Arctic Alpine ice core etc. As a part of the ongoing ABMs programme at 14UD Pelletron Accelerator Facility at Mumbai, a segmented gas detector developed for identification of 36Cl was tested for performance. Recently a beam chopper required for this measurement has been developed. Further progress made in this programme is discussed in this paper. (author)

  8. Mass spectrometry by means of tandem accelerators

    Mass spectrometry based on an accelerator allows to measure rare cosmogenic isotopes found in natural samples with isotopic abundances up to 10E-15. The XTU Tandem of Legnaro National Laboratories can measure mean heavy isotopes (36Cl, 41Ca, 129I) in applications interesting cosmochronology and Medicine. The TTT-3 Tandem of the Naples University has been modified in view of precision studies of C14 in Archeology, Paleantology and Geology. In this paper a review is made of principles and methodologies and of some applicationy in the framework of the National Program for mass spectrametry research with the aid of accelerators

  9. The high-precision Penning trap mass spectrometer PENTATRAP

    Doerr, Andreas; Bekker, Hendrik; Blaum, Klaus; Goncharov, Mikhail; Hoekel-Schmoeger, Christian [Max-Planck-Institut fuer Kernphysik, Heidelberg (Germany); Fakultaet fuer Physik und Astronomie, Ruprecht-Karls-Universitaet, Heidelberg (Germany); Boehm, Christine [Max-Planck-Institut fuer Kernphysik, Heidelberg (Germany); Fakultaet fuer Physik und Astronomie, Ruprecht-Karls-Universitaet, Heidelberg (Germany); Extreme Matter Institute EMMI, Helmholtz Gemeinschaft, Darmstadt (Germany); Crespo Lopez-Urrutia, Jose; Eliseev, Sergey; Repp, Julia; Roux, Christian; Sturm, Sven [Max-Planck-Institut fuer Kernphysik, Heidelberg (Germany); Novikov, Yuri [Petersburg Nuclear Physics Institute, Gatchina (Russian Federation); Ulmer, Stefan [Max-Planck-Institut fuer Kernphysik, Heidelberg (Germany); RIKEN Advanced Science Institute, Hirosawa, Wako, Saitama (Japan)

    2013-07-01

    Currently, the high-precision Penning trap mass spectrometer PENTATRAP is being built up at the Max-Planck-Institut fuer Kernphysik, Heidelberg, Germany. It aims at mass-ratio measurements of medium- to high-Z elements with uncertainties of a few parts in 10{sup 12}. Mass-ratios will be determined by the measurement of cyclotron frequency-ratios in the strong magnetic field of the trap. The experiment will host five identical cylindrical Penning traps and will allow for simultaneous cyclotron frequency determinations in all measurement traps. It will feature access to highly charged ions provided by EBITs. Measurements at PENTATRAP will contribute to various fields of physics. For example, input parameters for neutrino mass determinations will be provided with measurements of Q-values of relevant β-transitions. The current status of the experiment will be outlined in the talk.

  10. Ion mobility analyzer - quadrupole mass spectrometer system design

    Cuna, C; Leuca, M; Lupsa, N; Mirel, V; Cuna, Stela; Cosma, V; Tusa, Florina [National Institute for Research and Development of Isotopic and Molecular Technologies, 65-103 Donath, 400293 Cluj-Napoca (Romania); Bocos-Bintintan, V, E-mail: cornel.cuna@itim-cj.r [Babes-Bolyai University, Faculty of Environmental Sciences, 3 Fantanele, 400294 Cluj Napoca (Romania)

    2009-08-01

    Because of their extremely high sensitivity for chemicals with elevated electronegativity or high proton affinity the ion mobility analysers are ideal for the ultra-trace detection of toxic or explosive chemicals, most of these situated often at concentration levels of sub-ppb (parts-per-billion). Ion mobility spectrometers (IMS) can be used to identify illicit drugs or environmental pollutants. Since resolution of an IMS is relatively low, to achieve an accurate identification of target analyte it is recommended to couple the IMS with a quadrupole mass spectrometer (QMS) or a time of flight mass spectrometer, acquiring in this way confirmatory information. This coupling is made through a specific interface. In this paper, an experimental model of such a tandem instrument, IMS-QMS is described. Accomplishment of this general purpose will be done, overcoming a series of specific issues. This implies the solving, using innovative solutions, of a series of complex issues: ensuring the stability of the ions beam generated by ion source; transfer with a good efficiency of the ionic current from IMS analyser to QMS; and realization of a special electronic circuitry which will be able to detect both positive and negative ions.

  11. Ion mobility analyzer - quadrupole mass spectrometer system design

    Because of their extremely high sensitivity for chemicals with elevated electronegativity or high proton affinity the ion mobility analysers are ideal for the ultra-trace detection of toxic or explosive chemicals, most of these situated often at concentration levels of sub-ppb (parts-per-billion). Ion mobility spectrometers (IMS) can be used to identify illicit drugs or environmental pollutants. Since resolution of an IMS is relatively low, to achieve an accurate identification of target analyte it is recommended to couple the IMS with a quadrupole mass spectrometer (QMS) or a time of flight mass spectrometer, acquiring in this way confirmatory information. This coupling is made through a specific interface. In this paper, an experimental model of such a tandem instrument, IMS-QMS is described. Accomplishment of this general purpose will be done, overcoming a series of specific issues. This implies the solving, using innovative solutions, of a series of complex issues: ensuring the stability of the ions beam generated by ion source; transfer with a good efficiency of the ionic current from IMS analyser to QMS; and realization of a special electronic circuitry which will be able to detect both positive and negative ions.

  12. Non-accelerator neutrino mass searches

    Zuber, K.

    2000-01-01

    The current status of non-accelerator based searches for effects of a non-vanishing neutrino mass is reviewed. Beside the direct kinematical methods this includes searches for magnetic moments and a discussion of the solar neutrino problem. Double beta decay is not included.

  13. Linear electric field time-of-flight ion mass spectrometer

    Funsten, Herbert O.; Feldman, William C.

    2008-06-10

    A linear electric field ion mass spectrometer having an evacuated enclosure with means for generating a linear electric field located in the evacuated enclosure and means for injecting a sample material into the linear electric field. A source of pulsed ionizing radiation injects ionizing radiation into the linear electric field to ionize atoms or molecules of the sample material, and timing means determine the time elapsed between ionization of atoms or molecules and arrival of an ion out of the ionized atoms or molecules at a predetermined position.

  14. Instruction manual for ORNL tandem high abundance sensitivity mass spectrometer

    Smith, D.H.; McKown, H.S.; Chrisite, W.H.; Walker, R.L.; Carter, J.A.

    1976-06-01

    This manual describes the physical characteristics of the tandem mass spectrometer built by Oak Ridge National Laboratory for the International Atomic Energy Agency. Specific requirements met include ability to run small samples, high abundance sensitivity, good precision and accuracy, and adequate sample throughput. The instrument is capable of running uranium samples as small as 10/sup -12/ g and has an abundance sensitivity in excess of 10/sup 6/. Precision and accuracy are enhanced by a special sweep control circuit. Sample throughput is 6 to 12 samples per day. Operating instructions are also given.

  15. A gas monitoring facility with a quadrupole mass spectrometer for the ZEUS transition-radiation chambers

    A gas analysis facility for the ZEUS transition-radiation chambers based on a quadrupole mass spectrometer is described. After a description of the spectrometer, the vacuum system, and the software, some test results are presented. (HSI)

  16. One-step membrane feed system for a mass spectrometer

    The data on the gas permeability of membranes made of the Soviet silicon rubber which are used in the feed system for a mass spectrometer to analyze gaseous mixtures and gases dissolved in the liquid at atmospheric and increased pressures, are presented. Membranes of a rubber mixture have been made in the form of tubes with the wall thickness of outer and inner diameters of approximately 0.15 mm and 1 mm, respectively. No alterations in the mumbrane permeability at the measurement accuracy level of 5-10 % have been noticed in the process of investigations into the gaseous mixture composition at the atmospheric pressure during 500 hours with the total exploitation time of one year. The temperature increase from 22 to 35 deg C leads to the increase of nitrogen permeability by 35%. No mutual effect on the permeability is noticed for the mixture of N2, O2, C2 gases. The gas dynamic time constant of membranes is 3-5 s. The results obtained permit to consider one-step membrane feed systems for mass-spectrometers to be perspective when studying the composition of gaseous and liquid media in a wide range of pressures

  17. Accelerator Mass Spectrometry: practice and prospects

    Accelerator mass spectrometry (AMS) is an established technique for detecting rare isotopes, at isotope ratios in the range ∼10-12 to ∼10-15. As the name indicates, the technique uses an accelerator to produce high-energy ion beams, which are then analyzed by mass spectrometry. AMS is not only useful for determining anthropogenic or cosmogenic isotopes, but can also be used for trace element analysis, because every element except In has an isotope for which no other element has a stable isobar. This is significant for semiconductors and mineral analysis. The success of AMS arises from three factors: the use of negative ions at injection, which can suppress isobars (e.g.in the case of C-14); the stripping process at the accelerator terminal, which destroys molecular ions; and the high energy of the accelerated particles, which, by overcoming detector background, permits the use of sensitive particle identification and detection techniques. The 'standard' AMS isotopes are Be-10, C-14, Al-26, Cl-36, Ca-41, Ni-59, I-129. Prospective isotopes include Mn-53, Fe-60, Se-79, Tc-99, Pd-107, Sn-126, Cs-135. The following developed or prospective techniques are briefly discussed: total stripping; resonant ionization; static electric field ionization; the gas-filled magnet; isobaric laundering; negative molecular ions; laser photodetachment; X-ray identification. 9 refs., 4 tabs

  18. Accelerator mass spectrometry for radiocarbon dating

    Bronk, Christopher Ramsey.; Hedges, Robert; Robert Hedges

    1987-01-01

    Accelerator mass spectrometry (AMS) has been used routinely for radiocarbon measurements for several years. During this period it has become evident neither the accuracy nor the range of the technique were as great as had originally been hoped. This thesis describes both theoretical work to understand the reasons for this and practical solutions to overcome some of the problems. The production and transport of the ions used in the measurements are found to be the most crucial stages in...

  19. The five-Penning trap mass spectrometer PENTATRAP

    Repp, Julia; Boehm, Christine; Goncharov, Mikhail; Roux, Christian; Blaum, Klaus [Max-Planck-Institut fuer Kernphysik, 69117 Heidelberg (Germany); Physikalisches Institut, Ruprecht-Karls-Universitaet, 69120 Heidelberg (Germany); Crespo Lopez-Urrutia, Jose; Eliseev, Sergey [Max-Planck-Institut fuer Kernphysik, 69117 Heidelberg (Germany); Doerr, Andreas [Physikalisches Institut, Ruprecht-Karls-Universitaet, 69120 Heidelberg (Germany); Novikov, Yuri [St. Petersburg Nuclear Physics Institute, 188300 Gatchina (Russian Federation); Sturm, Sven [Johannes Gutenberg-Universitaet, Institut fuer Physik, 55099 Mainz (Germany); Ulmer, Stefan [Physikalisches Institut, Ruprecht-Karls-Universitaet, 69120 Heidelberg (Germany); Johannes Gutenberg-Universitaet, Institut fuer Physik, 55099 Mainz (Germany)

    2011-07-01

    Currently the new mass spectrometer PENTATRAP is being developed at the Max-Planck-Institut fuer Kernphysik in Heidelberg. Ions of interest are stable and long-lived highly charged nuclides up to uranium. PENTATRAP aims for an accuracy of few parts in 10{sup 12} for mass ratios of mass doublets and a relative uncertainty of {approx} 10{sup -11} for absolute mass ratios. The measured mass values will contribute among others to Q-value determinations of relevant {beta}-processes for neutrino physics, stringent tests of quantum electrodynamics in the regime of extreme fields, and a test of special relativity. The five-trap setup allows to choose an optimal measurement scheme for each ionic species of interest. Main features of PENTATRAP are an access to highly charged ions, highly sensitive cryogenic non-destructive detection systems, a fast exchange between different ions and a continuous monitoring of magnetic field fluctuations. This talk presents the experimental setup and the present status of the PENTATRAP experiment.

  20. Quantitative determination of carbonaceous particle mixing state in Paris using single particle mass spectrometer and aerosol mass spectrometer measurements

    Healy, R. M.; Sciare, J.; Poulain, L.; Crippa, M.; Wiedensohler, A.; Prévôt, A. S. H.; Baltensperger, U.; Sarda-Estève, R.; McGuire, M. L.; Jeong, C.-H.; McGillicuddy, E.; O'Connor, I. P.; Sodeau, J. R.; Evans, G. J.; Wenger, J. C.

    2013-04-01

    Single particle mixing state information can be a powerful tool for assessing the relative impact of local and regional sources of ambient particulate matter in urban environments. However, quantitative mixing state data are challenging to obtain using single particle mass spectrometers. In this study, the quantitative chemical composition of carbonaceous single particles has been estimated using an aerosol time-of-flight mass spectrometer (ATOFMS) as part of the MEGAPOLI 2010 winter campaign in Paris, France. Relative peak areas of marker ions for elemental carbon (EC), organic aerosol (OA), ammonium, nitrate, sulphate and potassium were compared with concurrent measurements from an Aerodyne high resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS), a thermal/optical OCEC analyser and a particle into liquid sampler coupled with ion chromatography (PILS-IC). ATOFMS-derived mass concentrations reproduced the variability of these species well (R2 = 0.67-0.78), and ten discrete mixing states for carbonaceous particles were identified and quantified. Potassium content was used to identify particles associated with biomass combustion. The chemical mixing state of HR-ToF-AMS organic aerosol factors, resolved using positive matrix factorization, was also investigated through comparison with the ATOFMS dataset. The results indicate that hydrocarbon-like OA (HOA) detected in Paris is associated with two EC-rich mixing states which differ in their relative sulphate content, while fresh biomass burning OA (BBOA) is associated with two mixing states which differ significantly in their OA/EC ratios. Aged biomass burning OA (OOA2-BBOA) was found to be significantly internally mixed with nitrate, while secondary, oxidized OA (OOA) was associated with five particle mixing states, each exhibiting different relative secondary inorganic ion content. Externally mixed secondary organic aerosol was not observed. These findings demonstrate the heterogeneity of primary and

  1. Quantitative determination of carbonaceous particle mixing state in Paris using single-particle mass spectrometer and aerosol mass spectrometer measurements

    R. M. Healy

    2013-09-01

    Full Text Available Single-particle mixing state information can be a powerful tool for assessing the relative impact of local and regional sources of ambient particulate matter in urban environments. However, quantitative mixing state data are challenging to obtain using single-particle mass spectrometers. In this study, the quantitative chemical composition of carbonaceous single particles has been determined using an aerosol time-of-flight mass spectrometer (ATOFMS as part of the MEGAPOLI 2010 winter campaign in Paris, France. Relative peak areas of marker ions for elemental carbon (EC, organic aerosol (OA, ammonium, nitrate, sulfate and potassium were compared with concurrent measurements from an Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS, a thermal–optical OCEC analyser and a particle into liquid sampler coupled with ion chromatography (PILS-IC. ATOFMS-derived estimated mass concentrations reproduced the variability of these species well (R2 = 0.67–0.78, and 10 discrete mixing states for carbonaceous particles were identified and quantified. The chemical mixing state of HR-ToF-AMS organic aerosol factors, resolved using positive matrix factorisation, was also investigated through comparison with the ATOFMS dataset. The results indicate that hydrocarbon-like OA (HOA detected in Paris is associated with two EC-rich mixing states which differ in their relative sulfate content, while fresh biomass burning OA (BBOA is associated with two mixing states which differ significantly in their OA / EC ratios. Aged biomass burning OA (OOA2-BBOA was found to be significantly internally mixed with nitrate, while secondary, oxidised OA (OOA was associated with five particle mixing states, each exhibiting different relative secondary inorganic ion content. Externally mixed secondary organic aerosol was not observed. These findings demonstrate the range of primary and secondary organic aerosol mixing states in Paris. Examination of the

  2. Quantitative determination of carbonaceous particle mixing state in Paris using single particle mass spectrometer and aerosol mass spectrometer measurements

    R. M. Healy

    2013-04-01

    Full Text Available Single particle mixing state information can be a powerful tool for assessing the relative impact of local and regional sources of ambient particulate matter in urban environments. However, quantitative mixing state data are challenging to obtain using single particle mass spectrometers. In this study, the quantitative chemical composition of carbonaceous single particles has been estimated using an aerosol time-of-flight mass spectrometer (ATOFMS as part of the MEGAPOLI 2010 winter campaign in Paris, France. Relative peak areas of marker ions for elemental carbon (EC, organic aerosol (OA, ammonium, nitrate, sulphate and potassium were compared with concurrent measurements from an Aerodyne high resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS, a thermal/optical OCEC analyser and a particle into liquid sampler coupled with ion chromatography (PILS-IC. ATOFMS-derived mass concentrations reproduced the variability of these species well (R2 = 0.67–0.78, and ten discrete mixing states for carbonaceous particles were identified and quantified. Potassium content was used to identify particles associated with biomass combustion. The chemical mixing state of HR-ToF-AMS organic aerosol factors, resolved using positive matrix factorization, was also investigated through comparison with the ATOFMS dataset. The results indicate that hydrocarbon-like OA (HOA detected in Paris is associated with two EC-rich mixing states which differ in their relative sulphate content, while fresh biomass burning OA (BBOA is associated with two mixing states which differ significantly in their OA/EC ratios. Aged biomass burning OA (OOA2-BBOA was found to be significantly internally mixed with nitrate, while secondary, oxidized OA (OOA was associated with five particle mixing states, each exhibiting different relative secondary inorganic ion content. Externally mixed secondary organic aerosol was not observed. These findings demonstrate the heterogeneity of

  3. Quantitative determination of carbonaceous particle mixing state in Paris using single-particle mass spectrometer and aerosol mass spectrometer measurements

    Healy, R. M.; Sciare, J.; Poulain, L.; Crippa, M.; Wiedensohler, A.; Prévôt, A. S. H.; Baltensperger, U.; Sarda-Estève, R.; McGuire, M. L.; Jeong, C.-H.; McGillicuddy, E.; O'Connor, I. P.; Sodeau, J. R.; Evans, G. J.; Wenger, J. C.

    2013-09-01

    Single-particle mixing state information can be a powerful tool for assessing the relative impact of local and regional sources of ambient particulate matter in urban environments. However, quantitative mixing state data are challenging to obtain using single-particle mass spectrometers. In this study, the quantitative chemical composition of carbonaceous single particles has been determined using an aerosol time-of-flight mass spectrometer (ATOFMS) as part of the MEGAPOLI 2010 winter campaign in Paris, France. Relative peak areas of marker ions for elemental carbon (EC), organic aerosol (OA), ammonium, nitrate, sulfate and potassium were compared with concurrent measurements from an Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS), a thermal-optical OCEC analyser and a particle into liquid sampler coupled with ion chromatography (PILS-IC). ATOFMS-derived estimated mass concentrations reproduced the variability of these species well (R2 = 0.67-0.78), and 10 discrete mixing states for carbonaceous particles were identified and quantified. The chemical mixing state of HR-ToF-AMS organic aerosol factors, resolved using positive matrix factorisation, was also investigated through comparison with the ATOFMS dataset. The results indicate that hydrocarbon-like OA (HOA) detected in Paris is associated with two EC-rich mixing states which differ in their relative sulfate content, while fresh biomass burning OA (BBOA) is associated with two mixing states which differ significantly in their OA / EC ratios. Aged biomass burning OA (OOA2-BBOA) was found to be significantly internally mixed with nitrate, while secondary, oxidised OA (OOA) was associated with five particle mixing states, each exhibiting different relative secondary inorganic ion content. Externally mixed secondary organic aerosol was not observed. These findings demonstrate the range of primary and secondary organic aerosol mixing states in Paris. Examination of the temporal

  4. The advantages of orthogonal acceleration in ICP time-of-flight mass spectrometry

    The OptiMass 8000 incorporates an orthogonal acceleration time-of-flight mass spectrometer. A general schematic of the instrument is given. The continuous ion beam is chopped by an orthogonal accelerator. A push out pulse supply is coupled to the accelerator for providing repetitive push-out voltages at a frequency of 30 kHz. The ion packets that are sliced out of the beam then travel within the field free space towards the SMARTGATE ion blanker. Orthogonal accelerator parameters are set to enable temporal-spatial focusing at the SMARTGATE ion blanker, so that iso-mass ion packets are resolved in time. Any ion packets of unwanted specie are ejected from the direction of travel by supplying pulsed voltages onto the deflection plates of the SMARTGATE. The ions to be measured are let through SMARTGATE and travel further down the field free space, to enter the ion reflectron. The ion reflectron increases the resolution of the mass spectrometer by means of temporal-energy focussing. After reflection, the ions travel within the field free space towards the discrete-dynode detector. In comparison to other acceleration geometries used in elemental time-of-flight mass spectrometry the OptiMass 8000 orthogonal acceleration geometry ultimately leads to superior resolution. As the energy spread is about 3 orders of magnitude lower in the time-of-flight direction for an oaTOFMS in comparison to an on-axis system, aberration acquired in the initial stages of acceleration are much lower. As a result the orthogonal acceleration scheme provides superior resolution at the first spatial focus point and the detector. The orthogonal acceleration time-of-flight analyzer of the OptiMass 8000 is able to provide resolution of at least 1800 at mass 238. (author)

  5. Broadband Single-Shot Electron Spectrometer for GeV-Class Laser Plasma Based Accelerators

    Nakamura, K.; Wan, W.; Ybarrolaza, N.; Syversrud, D.; Wallig, J.; Leemans, W.P.

    2008-05-01

    Laser-plasma-based accelerators can provide electrons over a broad energy range and/or with large momentum spread. The electron beam energy distribution can be controlled via accurate control of laser and plasma properties, and beams with energies ranging from'0.5 to 1000 MeV have been observed. Measuring these energy distributions in a single shot requires the use of a diagnostic with large momentum acceptance and, ideally, sufficient resolution to accurately measure energy spread in the case of narrow energy spread. Such a broadband single-shot electron magnetic spectrometer for GeV-class laser-plasma-based accelerators has been developed at Lawrence Berkeley National Laboratory. A detailed description of the hardware and the design concept is presented, as well as a performance evaluation of the spectrometer. The spectrometer covered electron beam energies raging from 0.01 to 1.1 GeV in a single shot, and enabled the simultaneous measurement of the laser properties at the exit of the accelerator through the use of a sufficiently large pole gap. Based on measured field maps and 3rd-order transport analysis, a few percent-level resolution and determination of the absolute energy were achieved over the entire energy range. Laser-plasma-based accelerator experiments demonstrated the capability of the spectrometer as a diagnostic and its suitability for such a broadband electron source.

  6. Multi-stage magnetic induction mass accelerator

    The magnetic induction method of mass acceleration readily lends itself to multi-staging. In the limit of many stages, such an accelerator approaches a distributed energy source system where only closing switches are necessary. We describe the design and performance of a three-stage accelerator, each driven by a separate capacitor bank. This system was modeled using a previously reported computer code. In order to do this the code was modified to calculate projectile acceleration through a succession of driver coils: Thermal conductivity and surface melting models were also added. The former is necessary due to the extended transit time through many stages. The latter is needed in anticipation of the more extreme ohmic heating when the capacitor banks are replaced by explosive-driven, magnetic flux compression generators. The performance goal of this system is to at least double the kinetic energy of a 0.3 kgm copperclad, steel projectile injected at a velocity of 300 m/sec from an explosive-driven gun. We then plan to test the system at the thermal and mechanical limit by using explosive-driven, magnetic flux compression generators as energy sources. We envision a six-stage system driven by three generators

  7. Mass measurements near the $r$-process path using the Canadian Penning Trap mass spectrometer

    Van Schelt, J.; Lascar, D.; G. Savard; Clark, J. A.; Caldwell, S.; Chaudhuri, A.; Fallis, J.; Greene, J. P.; Levand, 1 A. F.; Li, G.; Sharma, K. S.; Sternberg, M. G.; Sun, T.; Zabransky, B. J.

    2012-01-01

    The masses of 40 neutron-rich nuclides from Z = 51 to 64 were measured at an average precision of $\\delta m/m= 10^{-7}$ using the Canadian Penning Trap mass spectrometer at Argonne National Laboratory. The measurements, of fission fragments from a $^{252}$Cf spontaneous fission source in a helium gas catcher, approach the predicted path of the astrophysical $r$ process. Where overlap exists, this data set is largely consistent with previous measurements from Penning traps, storage rings, and ...

  8. Electrical recording system for laser mass spectrometer with double focusing

    Paper describes a system to record ion currents for EMAL-2 laser mass spectrometer with double focusing. The recording system consists of an original geometry multichannel collector, a controlled multiplexer and a data entry circuit. A receiving collector represents a set of metal plates separated by insulator plates of similar thickness. The collector has 384 channels at 38.4 cm length and 0.5 mm thickness of one collector unit. Every collector is put under condenser load. To measure discharge at accumulating systems and to enter data to a computer one applies a multichannel analog-to-digital converter (ADC) and a controlled multiplexer. One elaborated a special software enabling on-line displaying of signals from ADC

  9. Actinides analysis by accelerator mass spectrometry

    At the ANTARES accelerator at ANSTO a new beamline has been commissioned, incorporating new magnetic and electrostatic analysers, to optimise the efficiency for Actinides detection by Accelerator Mass Spectrometry (AMS). The detection of Actinides, particularly the isotopic ratios of uranium and plutonium, provide unique signatures for nuclear safeguards purposes. We are currently engaged in a project to evaluate the application of AMS to the measurement of Actinides in environmental samples for nuclear safeguards. Levels of certain fission products, Actinides and other radioactive species can be used as indicators of undeclared nuclear facilities or activities, either on-going or in the past Other applications of ultra-sensitive detection of Actinides are also under consideration. neutron-attenuation images of a porous reservoir rock

  10. Diagnostics aid for mass spectrometer trouble-shooting

    The ''MS Expert'' system provides problem diagnostics for instruments used in the Mass Spectrometry Laboratory (MSL). The most critical results generated on these mass spectrometers are the uranium concentration and isotopic content data used for process control and materials accountability at the Idaho Chemical Processing Plant. The two purposes of the system are: (1) to minimize instrument downtime and thereby provide the best possible support to the Plant, and (2) to improve long-term data quality. This system combines the knowledge of several experts on mass spectrometry to provide a diagnostic tool, and can make these skills avilable on a more timely basis. It integrates code written in the Pascal language with a knowledge base entered into a commercial expert system ''shell.'' The user performs some preliminary status checks, and then selects from among several broad diagnostic categories. These initial steps provide input to the rule base. The overall analysis provides the user with a set of possible solutions to the observed problems, graded as to their probabilities. Besides the trouble-shooting benefits expected from this system, it will also provide structures diagnostic training for lab personnel. In addition, development of the system knowledge base has already produced a better understanding of instrument behavior. Two key findings are that a good user interface is necessary for full acceptance of the tool, and a development system should include standard programming capabilities as well as the expert system shell. 22 refs., 5 figs

  11. Diagnostics aid for mass spectrometer trouble-shooting

    The MS Expert system provides problem diagnostics for instruments used in the Mass Spectrometry Laboratory (MSL). The most critical results generated on these mass spectrometers are the uranium concentration and isotopic content data used for process control and materials accountability at the Idaho General Processing Plant. The two purposes of the system are: (1) to minimize instrument downtime and thereby provide the best possible support to the Plant, and (2) to improve long-term data quality. This system combines the knowledge of several experts on mass spectrometry to provide a diagnostic tool, and can make these skills available on a more timely basis. It integrates code written in the Pascal language with a knowledge base entered into a commercial expert system shell. The user performs some preliminary status checks, and then selects from among several broad diagnostic categories. These initial steps provide input to the rule base. The overall analysis provides the user with a set of possible solutions to the observed problems, graded as to their probabilities. Besides the trouble-shooting benefits expected from this system, it also provides structured diagnostic training for lab personnel. In addition, development of the system knowledge base has already produced a better understanding of instrument behavior. Two key findings are that a good user interface is necessary for full acceptance of the tool, and, a development system should include standard programming capabilities as well as the expert system shell

  12. New directions for accelerator mass spectrometry technology

    The influence on accelerator mass spectrometry (AMS) of developments in other fields is reviewed and three examples are discussed in detail. The appropriate use of electric and magnetic analysers with small AMS systems (129I, for nuclear fuel monitoring and ocean circulation tracer studies. The inclusion of gas chromatography technology extends the capability of AMS to applications which require large numbers of samples with rapid turn-around. The adaptation of chemical reaction cell technology to negative ion beams adds new isobar selection capability to AMS and will permit analyses of isotopes such as 36Cl on small AMS systems. (author)

  13. 10 K Ring Electrode Trap - Tandem Mass Spectrometer for Infrared Spectroscopy of Mass Selected Ions

    A novel instrumental setup for measuring infrared photodissociation spectra of buffer gas cooled, mass-selected ions is described and tested. It combines a cryogenically cooled, linear radio frequency ion trap with a tandem mass spectrometer, optimally coupling continuous ion sources to pulsed laser experiments. The use of six independently adjustable DC potentials superimposed over the trapping radio frequency field provides control over the ion distribution within, as well as the kinetic energy distribution of the ions extracted from the ion trap. The scheme allows focusing the ions in space and time, such that they can be optimally irradiated by a pulsed, widely tunable infrared photodissociation laser. Ion intensities are monitored with a time-of-flight mass spectrometer mounted orthogonally to the ion trap axis.

  14. 10 K Ring Electrode Trap—Tandem Mass Spectrometer for Infrared Spectroscopy of Mass Selected Ions

    Goebbert, Daniel J.; Meijer, Gerard; Asmis, Knut R.

    2009-03-01

    A novel instrumental setup for measuring infrared photodissociation spectra of buffer gas cooled, mass-selected ions is described and tested. It combines a cryogenically cooled, linear radio frequency ion trap with a tandem mass spectrometer, optimally coupling continuous ion sources to pulsed laser experiments. The use of six independently adjustable DC potentials superimposed over the trapping radio frequency field provides control over the ion distribution within, as well as the kinetic energy distribution of the ions extracted from the ion trap. The scheme allows focusing the ions in space and time, such that they can be optimally irradiated by a pulsed, widely tunable infrared photodissociation laser. Ion intensities are monitored with a time-of-flight mass spectrometer mounted orthogonally to the ion trap axis.

  15. Fast mass programming controller for a supersonic gas chromatography mass spectrometer

    In a gas chromatograph mass spectrometer employing a quadrupole mass filter, molecules are ionized and transferred to a mass analyzer, where their mass to charge ratios (m/z) are measured. After the ionization step, the ions pass through a series of ion lenses that focus and guide them into the mass analyzer. The voltages on these lenses can be optimized for each specific m/z value (as the rest of the system is also optimized) to increase the number of ions reaching the mass analyzer. In certain cases, this dynamic mass-dependent optimization of the lenses can increase the signal by a factor of 2 or more. To implement this dynamic optimization, a digital circuit was developed, based on a digital signal controller and high-voltage (HV) amplifiers, that is able to optimize eight independent HV channels ranging between ±150 V at a rate of 100 µs

  16. Accelerator mass spectrometry for radiocarbon dating

    Accelerator mass spectrometry (AMS) has been used routinely for radiocarbon measurements for several years. This thesis describes theoretical work to understand the reasons for low accuracy and range and offers practical solutions. The production and transport of the ions used in the measurements are found to be the most crucial stages in the process. The theories behind ion production by sputtering are discussed and applied to the specific case of carbon sputtered by caesium. Experimental evidence is also examined in relation to the theories. The phenomena of space charge and lens aberrations are discussed along with the interaction between ion beams and gas molecules in the vacuum. Computer programs for calculating phase space transformations are then described; these are designed to help investigations of the effects of space charge and aberrations on AMS measurements. Calculations using these programs are discussed in relation both to measured ion beam profiles in phase space and to the current dependent transmission of ions through the Oxford radiocarbon accelerator. Improvements have been made to this accelerator and these are discussed in the context of the calculations. C- ions are produced directly from carbon dioxide at the Middleton High Intensity Sputter Source. Experiments to evaluate the performance of such a source are described and detailed design criteria established. An ion source designed and built specifically for radiocarbon measurements using carbon dioxide is described. Experiments to evaluate its performance and investigate the underlying physical processes are discussed. (author)

  17. Determining gaseous composition of fluid inclusions with quadrupole mass spectrometer

    ZHU; Heping

    2002-01-01

    [1]Joseph, R. G., Stephen, E. K., Factors affecting gas analysis of inclusion fluid by quadrupole mass spectrometry, Geo-chimica et Acta, 1995, 59(19): 3977-3986.[2]Masakatsu, S., Takayuki, S., Naoto, T., Analysis of fluid inclusion gases from geothermal systems, using a rapid-scanning quadrupole mass spectrometer, Eur. J. Mineral., 1992, 4: 895-906.[3]Van den Kerkhof, A. M., Isochoric phase diagrams in the systems CO2-CH4 and CO2-N2: Application to fluid inclusions, Geochimica et Cosmochimica Acta, 1990, 54: 621-629.[4]Colin, B., Michael, P. S., Mass spectrometric determination of gases in individual fluid inclusions in natural minerals, Anal. Chem., 1986, 58: 1330-1333.[5]David, I. N., Fredrick, J. S., Analysis of volatiles in fluid inclusions by mass spectrometry, Chemical Geology, 1987, 61: 1-10.[6]Yoichi, M., Ryo, K., Takayuki, S. et al., Gas composition of fluid inclusion from the Mori Geothermal Reservoir, South-western Hokkaido, Japan, Resource Geology, 1997, 47(5): 283-291.[7]Lu Huanzhang, Guo Dijiang, Progress and trends of researches on fluid inclusions, Geological Review, 2000, 46(4): 385-392.[8]Xia Xinyu, Wang Xianbin, Chen Jiangfeng, Geningjie, composition of fluid inclusions and CO2 carbon isotope of ultra-high pressure metamorphic rocks in Shuanghe area, Dabieshan Mountain, Science in China (in Chinese), Ser. D, 1999, 29(4): 314-320.

  18. Miniature Ion Optics Towards a Micro Mass Spectrometer

    Chaudhary, Ashish

    This PhD dissertation reports the development of miniature ion optics components of a mass spectrometer (MS) with the ultimate goal to lay the foundation for a compact low-power micromachined MS (microMS) for broad-range chemical analysis. Miniaturization of two specific components a) RF ion traps and b) an ion funnel have been investigated and miniature low-power versions of these components have been developed and demonstrated successfully in lab experiments. Power savings, simpler electronics and packaging schemes required to operate the micro-scale RF cylindrical ion traps have been the key motivation driving this research. Microfabricated cylindrical ion traps (microCITs) and arrays in silicon, silicon-on-insulator and stainless steel substrates have been demonstrated and average power of as low as 55 mW for a low mass range (28 to 136 amu) and mass spectra with better than a unit-mass-resolution have been recorded. For the ion funnel miniaturization effort, simple assembly, small form factor and ease of integration have been emphasized. A simplification of the conventional 3D ion funnel design, called the planar ion funnel, has been developed in a single plate and has been tested to demonstrate ion funneling at medium vacuum levels (1E-5 Torr) using DC voltages and power less than 0.5 W. Miniaturization of these components also enables use of other novel ion optics components, packaging and integration, which will allow a new class of microMS architectures amenable for radical miniaturization.

  19. Recent results from the Penning trap mass spectrometer JYFLTRAP

    Accurate mass determination employing Penning ion traps has gained increasing importance after the installation of several new on-line facilities at accelerator labs. These setups combine unique production possibilities for rare isotopes with elaborate ion-capture and manipulation techniques. Since the final commissioning of the JYFLTRAP setup at the IGISOL facility in Jyvaeskylae, the masses of more than 200 short-lived nuclides have been measured. Their knowledge applies to studies on nuclear structure, the modeling of nucleosynthesis processes, tests of the conserved vector current (CVC) hypothesis and the unitarity of the CKM matrix, and furthermore, can help to assist in ongoing searches of neutrinoless double-beta decays. This presentation focuses on recent highlights studied at JYFLTRAP

  20. Recent results from the Penning trap mass spectrometer JYFLTRAP

    Weber, Christine; Elomaa, Viki-Veikko; Eronen, Tommi; Hakala, Jani; Jokinen, Ari; Kankainen, Anu; Rahaman, Saidur; Rissanen, Juho; Aeystoe, Juha [Department of Physics, (YFL), University of Jyvaeskylae (Finland)

    2009-07-01

    Accurate mass determination employing Penning ion traps has gained increasing importance after the installation of several new on-line facilities at accelerator labs. These setups combine unique production possibilities for rare isotopes with elaborate ion-capture and manipulation techniques. Since the final commissioning of the JYFLTRAP setup at the IGISOL facility in Jyvaeskylae, the masses of more than 200 short-lived nuclides have been measured. Their knowledge applies to studies on nuclear structure, the modeling of nucleosynthesis processes, tests of the conserved vector current (CVC) hypothesis and the unitarity of the CKM matrix, and furthermore, can help to assist in ongoing searches of neutrinoless double-beta decays. This presentation focuses on recent highlights studied at JYFLTRAP.

  1. Using a fully automatic mass spectrometer for fissile material control

    The demand for higher accuracy and a shorter delay in the analysis together with better objectifiability and data security needed in safeguards, lead to the automation of a mass spectrometer. Starting with a continuous feeding of samples via a high vacuum lock and including the subsequent heating, focussing and scanning of the samples as well as the final evaluation of the source data (taking alpha spectrometry and the weights required for the isotope dilution technique into account), the mass spectrometric procedure was completely automated. For this purpose, a serial CH-5 instrument of varian mat was modified to be operated by a varian 620/I computer. A newly developed three chamber high vacuum lock was attached to this system and the final evaluation is made with an IBM 370. The system has been used in operation for the isotope analysis of U, Pu and Nd for one year. Major breakdowns of the hardware did not occur, however, the computer programmes had to be steadily improved according to the changing characteristics of the samples. Compared to manual operation, the automat is superior in its throughput and speed of analysing series of similar samples. The automatic procedure objectifies the analysis and the complete evaluation ensures a better data security. (Orig./HP). (author)

  2. A New Multi Collector Isotope Ratio Mass Spectrometer

    Appelhans, A. D.; Olson, J. E.; Ward, M. B.; Dahl, D. A.

    2007-12-01

    With the goal of improving the sensitivity of isotope ratio measurements, particularly for actinides, a new magnetic sector mass spectrometer that utilizes up to seven full-sized discrete dynode electron multipliers operating simultaneously has been designed, constructed and is in the early stages of testing. The design is based on a newly developed ion dispersion lens that enables the mass dispersed individual isotope beams to be separated by 35 mm; this allows a full-sized discrete dynode pulse counting multiplier to be used for each beam. The ion dispersion lens (US patents 6,297,501 and pending) is a two element electrostatic 90 degree sector device that causes the beam-to-beam dispersion to increase faster than the intra-beam dispersion. Each of the multipliers is housed in an isolated case and is equipped with a deflector/condenser lens at the entrance to optimize pulse generation. The instrument includes a 9-sample filament cartridge mounted on a micro-manipulator X-Y stage that enables adjustment of the filament position with 10 micron resolution within the ion lens. Initial testing has shown that the instrument is performing as predicted by the ion optics model of the design.

  3. Detection electronics at the Penning trap mass spectrometer PENTATRAP

    Doerr, Andreas; Boehm, Christine; Repp, Julia; Roux, Christian; Blaum, Klaus [Physikalisches Institut, Ruprecht-Karls-Universitaet, 69120 Heidelberg (Germany); Max-Planck-Institut fuer Kernphysik, 69117 Heidelberg (Germany); Crespo Lopez-Urrutia, Jose; Eliseev, Sergey; Goncharov, Mikhail [Max-Planck-Institut fuer Kernphysik, 69117 Heidelberg (Germany); Novikov, Yuri [St. Petersburg Nuclear Physics Institute, 188300 Gatchina (Russian Federation); Sturm, Sven [Johannes Gutenberg-Universitaet, Institut fuer Physik, 55099 Mainz (Germany); Ulmer, Stefan [Physikalisches Institut, Ruprecht-Karls-Universitaet, 69120 Heidelberg (Germany); Johannes Gutenberg-Universitaet, Institut fuer Physik, 55099 Mainz (Germany)

    2011-07-01

    The ''five Penning trap'' mass spectrometer PENTATRAP is currently under construction at the Max-Planck-Institut fuer Kernphysik in Heidelberg. Measurements of masses of single stable and long lived highly charged ions with a relative uncertainty on the order of 10{sup -11} are aimed at. The experiment is based on the non-destructive detection of image currents the ion induces in the trap electrodes. Essential part of each detection circuit is an inductance, configured either as a copper wire coil or as a superconducting toroid, in both cases mounted in a copper housing. Since signals are small ({proportional_to}fA), low-noise detection electronics is needed to obtain a sufficient signal-to-noise ratio. Therefore the first amplification stage is a cryogenic GaAs amplifier. Currently, we evaluate the possible use of a SQUID based amplifier. Furthermore, an axial frequency down converter providing a high level of sideband rejection has been set up. Further details on the detection electronics mentioned above will be presented in the poster.

  4. Detection electronics at the Penning-trap mass spectrometer PENTATRAP

    Doerr, Andreas; Repp, Julia; Roux, Christian; Blaum, Klaus [Fakultaet fuer Physik und Astronomie, Ruprecht-Karls-Universitaet, 69120 Heidelberg (Germany); Max-Planck-Institut fuer Kernphysik, 69117 Heidelberg (Germany); Boehm, Christine [Fakultaet fuer Physik und Astronomie, Ruprecht-Karls-Universitaet, 69120 Heidelberg (Germany); Max-Planck-Institut fuer Kernphysik, 69117 Heidelberg (Germany); ExtreMe Matter Institute EMMI, Helmholtz Gemeinschaft, 64291 Darmstadt (Germany); Eliseev, Sergey; Goncharov, Mikhail [Max-Planck-Institut fuer Kernphysik, 69117 Heidelberg (Germany); Sturm, Sven [Max-Planck-Institut fuer Kernphysik, 69117 Heidelberg (Germany); Institut fuer Physik, Johannes Gutenberg-Universitaet, 55099 Mainz (Germany); Ulmer, Stefan [Atomic Physics Laboratory, RIKEN Advanced Science Institute, Hirosawa, Wako, Saitama 351-0198 (Japan)

    2012-07-01

    The five Penning-trap mass spectrometer PENTATRAP is currently being built at the Max-Planck-Institut fuer Kernphysik in Heidelberg. Measurements of masses of single stable and long lived highly charged ions with a relative uncertainty on the order of 10{sup -11} are aimed for. The experiment is based on the non-destructive detection of image currents the ion induces in the trap electrodes. Essential part of each detection circuit is a cryogenic high-Q inductance, configured either as a copper wire coil or as a superconducting toroid, in both cases mounted in a copper housing. The following amplification stages consist of cryogenic GaAs FET amplifiers, which provide high input impedances and have low input-related noise densities. With these cryogenic detection systems, the tiny image currents ({proportional_to}fA) induced by a single ion become detectable. The current status of the detection electronics as well as future perspectives are presented in the talk.

  5. High-precision masses of neutron-deficient rubidium isotopes using a Penning trap mass spectrometer

    Kellerbauer, A G; Beck, D; Blaum, K; Bollen, G; Guénaut, C; Herfurth, F; Herlert, A; Kluge, H J; Lunney, D; Schwarz, S; Schweikhard, L; Weber, C; Yazidjian, C

    2007-01-01

    The atomic masses of the neutron-deficient radioactive rubidium isotopes $^{74-77,79,80,83}$Rb have been measured with the Penning trap mass spectrometer ISOLTRAP. Using the time-of-flight cyclotron resonance technique, relative mass uncertainties ranging from $1.6 \\times 10^{-8}$ to $5.6 \\times 10^{-8}$ were achieved. In all cases, the mass precision was significantly improved as compared with the prior Atomic-Mass Evaluation; no significant deviations from the literature values were observed. The exotic nuclide $^{74}$Rb with a half-life of only 65 ms, is the shortest-lived nuclide on which a high-precision mass measurement in a Penning trap has been carried out. The significance of these measurements for a check of the conserved-vector-current hypothesis of the weak interaction and the unitarity of the Cabibbo-Kobayashi-Maskawa matrix is discussed.

  6. High-Precision Mass Measurements of Exotic Nuclei with the Triple-Trap Mass Spectrometer Isoltrap

    Blaum, K; Zuber, K T; Stanja, J

    2002-01-01

    The masses of close to 200 short-lived nuclides have already been measured with the mass spectrometer ISOLTRAP with a relative precision between 1$\\times$10$^{-7}$ and 1$\\times$10^{-8}$. The installatin of a radio-frequency quadrupole trap increased the overall efficiency by two orders of magnitude which is at present about 1%. In a recent upgrade, we installed a carbon cluster laser ion source, which will allow us to use carbon clusters as mass references for absolute mass measurements. Due to these improvements and the high reliability of ISOLTRAP we are now able to perform accurate high-precision mass measurements all over the nuclear chart. We propose therefore mass measurements on light, medium and heavy nuclides on both sides of the valley of stability in the coming four years. ISOLTRAP is presently the only instrument capable of the high precision required for many of the proposed studies.

  7. Mass Spectrometer Sounding of the Turbopause Region on Commercial Vehicles

    Thurairajah, B.; Bailey, S. M.; Syrstad, E. A.; Fish, C. S.; Siskind, D. E.; Russell, J. M.

    2013-12-01

    The turbopause region near 100 km remains one of the most poorly explored yet crucial regions of the upper atmosphere. In the vicinity of this altitude, the atmosphere reaches its lowest temperature and changes from being well mixed to being in diffusive equilibrium. Dynamical energy in the form of tides as well as gravity and planetary waves propagate from the lower atmosphere up to the ionosphere and thermosphere. Some energy and reactive chemical species are transported down across the turbopause to lower altitudes where the impact is significant. There is a significant dearth of composition observations near the turbopause. Few measurement techniques work well at this altitude, and it is too low for satellite orbits. Amazingly, major species with relatively large abundances such as O2, O, and CO2 are all poorly understood at these attitudes. While there are several experiments that measure temperature, the uncertainties in the temperature measurements are large because the techniques that are used rely on knowledge of CO2 or sometimes of O2. The lack of composition information thus hinders those observations that do occur near the turbopause and mesopause and leaves us with an overall poor understanding of this altitude region. We are soon to enter a new era in space exploration. Routine visits to the 100km region by commercial vehicles are on the verge of becoming a reality. The relevant organizations have expressed a willingness and even enthusiasm for including scientific instrumentation with their tourism and related commercial goals. We propose a major step forward in understanding the turbopause region by developing a mass spectrometer capable of being manifested on these commercial vehicles. Such an implantation could ultimately result in daily sounding of the turbopause region and greatly expand the database of measurements there. Our suggested instrument is a cryogenic time-of-flight mass Spectrometer. This technique has heritage, and our

  8. IBM PC based data acquisition and processing package for an organic mass spectrometer (VG micro mass 7070F)

    The manual processing and mass marking of data obtained from mass spectrometer through UV oscillograph is tedious and quite time consuming. This report describes interconnection of an IBM PC through an ADC interface to the mass spectrometer to acquire and store the mass spectral data and offline processing. A menu driven software in Turbo Pascal has been developed for this purpose which is described in detail. (author). 3 refs., 17 figs., 2 tabs

  9. Desorption electrospray ionization using an Orbitrap mass spectrometer: Exact mass measurements on drugs and peptides.

    Hu, Qizhi; Talaty, Nari; Noll, Robert J; Cooks, R Graham

    2006-01-01

    Desorption electrospray ionization (DESI) is implemented on an Orbitrap mass spectrometer. The ion source is described and applications which utilize the high-resolution capabilities of the Orbitrap are emphasized, including the characterization of peptides and active ingredients in pharmaceutical tablets. Measurements are made in less than 1 s at a resolution of 60,000. The implications of the data for the mechanisms of DESI are discussed. PMID:17051609

  10. Radiocarbon dating with accelerator mass spectrometry

    Radiocarbon dating by means of accelerator mass spectrometry (AMS) has two great advantages over conventional dating: 1) much smaller samples can be handled and 2) counting time is significantly shorter. Three examples are given for Holocene-age material from east-central Ellesmere Island. The results demonstrate the potential use of this technique as a powerful research tool in studies of Quaternary chronology. Individual fragments of marine shells as small as 0.1 g have been dated successfully at the IsoTrace Laboratory, University of Toronto. In the case of an aquatic moss from a lake sediment core, an increment 0.5 cm thick could be used instead of a 5 cm-thick slice, thus allowing a much more precise estimate of the onset of organic sedimentation

  11. Ambient mass spectrometry with a handheld mass spectrometer at high pressure.

    Keil, Adam; Talaty, Nari; Janfelt, Christian; Noll, Robert J; Gao, Liang; Ouyang, Zheng; Cooks, R Graham

    2007-10-15

    The first coupling of atmospheric pressure ionization methods, electrospray ionization (ESI) and desorption electrospray ionization (DESI), to a miniature hand-held mass spectrometer is reported. The instrument employs a rectilinear ion trap (RIT) mass analyzer and is battery-operated, hand-portable, and rugged (total system: 10 kg, 0.014 m(3), 75 W power consumption). The mass spectrometer was fitted with an atmospheric inlet, consisting of a 10 cm x 127 microm inner diameter stainless steel capillary tube which was used to introduce gas into the vacuum chamber at 13 mL/min. The operating pressure was 15 mTorr. Ions, generated by the atmospheric pressure ion source, were directed by the inlet along the axis of the ion trap, entering through an aperture in the dc-biased end plate, which was also operated as an ion gate. ESI and DESI sources were used to generate ions; ESI-MS analysis of an aqueous mixture of drugs yielded detection limits in the low parts-per-billion range. Signal response was linear over more than 3 orders of magnitude. Tandem mass spectrometry experiments were used to identify components of this mixture. ESI was also applied to the analysis of peptides and in this case multiply charged species were observed for compounds of molecular weight up to 1200 Da. Cocaine samples deposited or already present on different surfaces, including currency, were rapidly analyzed in situ by DESI. A geometry-independent version of the DESI ion source was also coupled to the miniature mass spectrometer. These results demonstrate that atmospheric pressure ionization can be implemented on simple portable mass spectrometry systems. PMID:17867653

  12. Reproducibility of cardioventilatory measurements using a respiratory mass spectrometer.

    Narang, Indra; Rosenthal, Mark; Bush, Andrew

    2007-08-01

    The aim of this study was to assess the within subject reproducibility of cardioventilatory measurements and the maximum permitted 'normal' variability over time at rest and exercise using the respiratory mass spectrometer (RMS). Ten subjects underwent an incremental exercise test on three separate occasions utilising rebreathing (RB) and helium dilution mixed expired gas analysis (HME) functions of the RMS. Measurements included heart rate (HR), oxygen consumption (V(O2)), carbon dioxide excretion (V(VO2)), effective pulmonary blood flow (Q(eff)), stroke volume (SV), arteriovenous oxygen content difference (AVO), transfer factor (Dl(CO)), functional residual capacity (FRC), minute ventilation (VE), tidal volume (VT) and respiratory quotient (RQ). The coefficients of variation for each variable for the 10 subjects were calculated. At rest, the 90th centile variability for measured cardiopulmonary variables (RB only) was <35%. During exercise, the 90th centile for variability for measured cardiopulmonary variables for HME and RB were < or =20 and <40%, respectively. These measurements in healthy adults should inform sample size in research studies. PMID:17188945

  13. SCAPS, a two-dimensional ion detector for mass spectrometer

    Yurimoto, Hisayoshi

    2014-05-01

    Faraday Cup (FC) and electron multiplier (EM) are of the most popular ion detector for mass spectrometer. FC is used for high-count-rate ion measurements and EM can detect from single ion. However, FC is difficult to detect lower intensities less than kilo-cps, and EM loses ion counts higher than Mega-cps. Thus, FC and EM are used complementary each other, but they both belong to zero-dimensional detector. On the other hand, micro channel plate (MCP) is a popular ion signal amplifier with two-dimensional capability, but additional detection system must be attached to detect the amplified signals. Two-dimensional readout for the MCP signals, however, have not achieve the level of FC and EM systems. A stacked CMOS active pixel sensor (SCAPS) has been developed to detect two-dimensional ion variations for a spatial area using semiconductor technology [1-8]. The SCAPS is an integrated type multi-detector, which is different from EM and FC, and is composed of more than 500×500 pixels (micro-detectors) for imaging of cm-area with a pixel of less than 20 µm in square. The SCAPS can be detected from single ion to 100 kilo-count ions per one pixel. Thus, SCAPS can be accumulated up to several giga-count ions for total pixels, i.e. for total imaging area. The SCAPS has been applied to stigmatic ion optics of secondary ion mass spectrometer, as a detector of isotope microscope [9]. The isotope microscope has capabilities of quantitative isotope images of hundred-micrometer area on a sample with sub-micrometer resolution and permil precision, and of two-dimensional mass spectrum on cm-scale of mass dispersion plane of a sector magnet with ten-micrometer resolution. The performance has been applied to two-dimensional isotope spatial distribution for mainly hydrogen, carbon, nitrogen and oxygen of natural (extra-terrestrial and terrestrial) samples and samples simulated natural processes [e.g. 10-17]. References: [1] Matsumoto, K., et al. (1993) IEEE Trans. Electron Dev. 40

  14. A collinear tandem time-of-flight mass spectrometer for infrared photodissociation spectroscopy of mass-selected ions

    WANG GuanJun; CHI ChaoXian; XING XiaoPeng; DING ChuanFan; ZHOU MingFei

    2014-01-01

    An apparatus based on collinear tandem time-of-flight mass spectrometer has been designed for the measurement of infrared photodissociation spectroscopy of mass-selected ions in the gas phase.The ions from a pulsed laser vaporization supersonic ion source are skimmed and mass separated by a Wiley-McLaren time-of-flight mass spectrometer.The ion of interest is mass selected,decelerated and dissociated by a tunable IR laser.The fragment and parent ions are reaccelerated and mass analyzed by the second time-of-flight mass spectrometer.A simple new assembly integrated with mass gate,deceleration and reacceleration ion optics was designed,which allows us to measure the infrared spectra of mass selected ions with high sensitivity and easy timing synchronization.

  15. The time-of-flight isochronous (TOFI) spectrometer for direct mass measurements of exotic light nuclei

    A new type of time-of-flight recoil spectrometer designed to measure the masses of neutron-rich light nuclei has recently been completed at LAMPF. The spectrometer relies on an isochronous design that directly correlates an ion's time-of-flight through the spectrometer with its mass-to-charge ratio. Additional measurements of the ion's velocity and energy enable the charge state of the recoil to be uniquely defined and thus permit precision mass measurements given sufficient statistics. The performance of the spectrometer has been investigated in both-off line (using alpha sources) and on-line tests. The design resolution of ΔM/M=1/2000 (fwhm) has been achieved. Initial performance results of the spectrometer are described with emphasis placed on the techniques used to achieve the overall high mass resolution and large solid angle/momentum acceptance. (orig.)

  16. The Time-of-Flight Isochronous (TOFI) spectrometer for direct mass measurements of exotic light nuclei

    A new type of time-of-flight recoil spectrometer designed to measure the masses of neutron-rich light nuclei has recently been completed at LAMPF. The spectrometer relies on an isochronous design that directly correlates an ion's time-of-flight through the spectrometer with it's mass-to-charge ratio. Additional measurements of the ion's velocity and energy enable the charge state of the recoil to be uniquely defined and thus permit precision mass measurements given sufficient statistics. The performance of the spectrometer has been investigated in both off-line (using alpha sources) and on-line tests. The design resolution of Δm/M = 1/2000 (FWHM) has been achieved. Initial performance results of the spectrometer are described with emphasis placed on the techniques used to achieve the overall high mass resolution and large solid angle/momentum acceptance

  17. SIEMENS ADVANCED QUANTRA FTICR MASS SPECTROMETER FOR ULTRA HIGH RESOLUTION AT LOW MASS

    Spencer, W; Laura Tovo, L

    2008-07-08

    The Siemens Advanced Quantra Fourier Transform Ion Cyclotron Resonance (FTICR) mass spectrometer was evaluated as an alternative instrument to large double focusing mass spectrometers for gas analysis. High resolution mass spectrometers capable of resolving the common mass isomers of the hydrogen isotopes are used to provide data for accurate loading of reservoirs and to monitor separation of tritium, deuterium, and helium. Conventional double focusing magnetic sector instruments have a resolution that is limited to about 5000. The Siemens FTICR instrument achieves resolution beyond 400,000 and could possibly resolve the tritium ion from the helium-3 ion, which differ by the weight of an electron, 0.00549 amu. Working with Y-12 and LANL, SRNL requested Siemens to modify their commercial Quantra system for low mass analysis. To achieve the required performance, Siemens had to increase the available waveform operating frequency from 5 MHz to 40 MHz and completely redesign the control electronics and software. However, they were able to use the previous ion trap, magnet, passive pump, and piezo-electric pulsed inlet valve design. NNSA invested $1M in this project and acquired four systems, two for Y-12 and one each for SRNL and LANL. Siemens claimed a $10M investment in the Quantra systems. The new Siemens Advanced Quantra demonstrated phenomenal resolution in the low mass range. Resolution greater than 400,000 was achieved for mass 2. The new spectrometer had a useful working mass range to 500 Daltons. However, experiments found that a continuous single scan from low mass to high was not possible. Two useful working ranges were established covering masses 1 to 6 and masses 12 to 500 for our studies. A compromise performance condition enabled masses 1 to 45 to be surveyed. The instrument was found to have a dynamic range of about three orders of magnitude and quantitative analysis is expected to be limited to around 5 percent without using complex fitting algorithms

  18. "Fast Excitation" CID in Quadrupole Ion Trap Mass Spectrometer

    Murrell, J. [Defence Science and Detection Department (Dstl), Wiltshire, UK; Despeyroux, D. [Defence Science and Detection Department (Dstl), Wiltshire, UK; Lammert, Stephen {Steve} A [ORNL; Stephenson Jr, James {Jim} L [ORNL; Goeringer, Doug [ORNL

    2003-01-01

    Collision-induced dissociation (CID) in a quadrupole ion trap mass spectrometer is usually performed by applying a small amplitude excitation voltage at the same secular frequency as the ion of interest. Here we disclose studies examining the use of large amplitude voltage excitations (applied for short periods of time) to cause fragmentation of the ions of interest. This process has been examined using leucine enkephalin as the model compound and the motion of the ions within the ion trap simulated using ITSIM. The resulting fragmentation information obtained is identical with that observed by conventional resonance excitation CID. ''Fast excitation'' CID deposits (as determined by the intensity ratio of the a{sub 4}/b{sub 4} ion of leucine enkephalin) approximately the same amount of internal energy into an ion as conventional resonance excitation CID where the excitation signal is applied for much longer periods of time. The major difference between the two excitation techniques is the higher rate of excitation (gain in kinetic energy) between successive collisions with helium atoms with ''fast excitation'' CID as opposed to the conventional resonance excitation CID. With conventional resonance excitation CID ions fragment while the excitation voltage is still being applied whereas for ''fast excitation'' CID a higher proportion of the ions fragment in the ion cooling time following the excitation pulse. The fragmentation of the (M + 17H){sup 17+} of horse heart myoglobin is also shown to illustrate the application of ''fast excitation'' CID to proteins.

  19. Plasma Desorption Mass Spectrometry using TANDEM accelerator in National Industrial Research Inst. of Nagoya

    Mizota, Takeshi; Nakao, Setsuo; Niwa, Hiroaki; Saito, Kazuo [Particle Beam Sceince Laboratory, Multi-Function Material Science Department, National Industrial Research Inst. of Nagoya, Nagoya (Japan)

    2001-02-01

    Plasma Desorption Mass Spectrometry (PDMS) analysis was studied using TANDEM accelerator. The heavy ions of MeV range emit the secondary ions of atoms, molecules, polymers and clusters from the irradiated samples without destruction. The analysis system of PDMS designed and set-up using a mass spectrometer of Time of Flight and the TANDEM accelerator. The system performance was tested for C-60 fullerene on the surface of the samples using 11.2 MeV {sup 28}Si beams produced by the TANDEM accelerator of 1.7MV. The result shows that the hydrogen and hydrocarbons can be analyzed in the range of 1amu unit. The resolution (M/{delta}M) of the Mass Spectrometry system is confirmed to be about 1000 from the separation of the 720 and 721amu peaks, which is attributed to the C-60 fullerene including {sup 13}C atoms. (H. Katsuta)

  20. Measurement of mass and isotopic fission yields for heavy fission products with the LOHENGRIN mass spectrometer

    In spite of the huge amount of fission yield data available in different libraries, more accurate values are still needed for nuclear energy applications and to improve our understanding of the fission process. Thus measurements of fission yields were performed at the mass spectrometer Lohengrin at the Institut Laue-Langevin in Grenoble, France. The mass separator Lohengrin is situated at the research reactor of the institute and permits the placement of an actinide layer in a high thermal neutron flux. It separates fragments according to their atomic mass, kinetic energy and ionic charge state by the action of magnetic and electric fields. Coupled to a high resolution ionization chamber the experiment was used to investigate the mass and isotopic yields of the light mass region. Almost all fission yields of isotopes from Th to Cf have been measured at Lohengrin with this method. To complete and improve the nuclear data libraries, these measurements have been extended in this work to the heavy mass region for the reactions 235U(nth,f), 239Pu(nth,f) and 241Pu(nth,f). For these higher masses an isotopic separation is no longer possible. So, a new method was undertaken with the reaction 239Pu(nth,f) to determine the isotopic yields by spectrometry. These experiments have allowed to reduce considerably the uncertainties. Moreover the ionic charge state and kinetic energy distributions were specifically studied and have shown, among others, nanosecond isomers for some masses. (author)

  1. A Micro Cylindrical Ion Trap (5-CIT) Micro Mass Spectrometer Instrument System (5MSIS) for NASA Planetary Exploration Project

    National Aeronautics and Space Administration — The project aims to develop a miniature packaging platform for the integration of MEMS mass spectrometer components to form the basis of a Micro Mass Spectrometer...

  2. Pluto Integrated Camera-Spectrometer (PICS): A Low Mass, Low Power Instrument for Planetary Exploration

    Beauchamp, Patricia; Brown, Robert; Rodgers, David; Chrisp, Michael; Chen, Gun-Shiog; Fraschetti, George; Krabach, Timothy; Petrick, Walter; Soderblom, Laurance; Yelle, Roger; Benoit, Robert; Curcio, Michael; Glasheen, Richard; Tucker, Theodore; Wang, Dexter

    1994-01-01

    The concept we describe is an integrated instrument (a Pluto Integrated Camera Spectrometer, PICS) that will perform the functions of all three optical instruments required by the Pluto Fast Flyby Mission: the near-IR spectrometer, the camera, and the UV spectrometer. This integrated approach minimizes mass and power use. It also forced us early in the conceptual design to consider integrated observational sequences and integrated power management, thus ensuring compatible duty cycles (i.e. e...

  3. Fundamental studies of MALDI with an orthogonal TOF mass spectrometer

    Qiao, Hui

    The interaction between the matrix and analyte molecules are studied with a high resolution MALDI imaging technique in an orthogonal-injection time of flight (TOF) mass spectrometer. The analyte incorporation and distribution patterns have been clearly demonstrated. Purified protein analytes were found to be homogeneously incorporated in large single crystals of DHB and sinapinic acid matrices, with no evidence for preferred crystal faces. Segregation of some species was observed and appeared to correlate with analyte hydrophobicity, and to a lesser extent analyte mass or mobility. Similar segregation phenomena were observed with confocal laser scanning microscopy of the same analytes labeled with fluorescent dyes in 2,5-DHB single crystals. The above investigations may shed some light on optimizing sample preparation with different matrices. The influence of incident laser parameters on sensitivity in MALDI has been investigated using orthogonal-injection TOF instruments. A qualitative comparison was first made between the beam profiles obtained with a N 2 laser and a Nd:YAG laser using 2-m long optical fibers. The N 2 laser gives better sensitivity, consistent with a more uniform fluence distribution and therefore better coverage of the N2 laser profile. Most of the difference disappears when a 30-m long fiber is used or when the fibers are twisted during irradiation to smooth out the fluence distribution. In more systematic measurements, the total integrated ion yield from a single spot (a measure of sensitivity) was found to increase rapidly with fluence to a maximum, and then saturate or decrease slightly. Thus, the optimum sensitivity is achieved at high fluence. For a fluence near threshold, the integrated yield has a steep (cubic) dependence on the spot size, but the yield saturates at higher fluence for smaller spots. The area dependence is much weaker (close to linear) for fluence values above saturation, with the result that the highest integrated yields

  4. Mass measurement of halo nuclides and beam cooling with the mass spectrometer Mistral

    Halo nuclides are a spectacular drip-line phenomenon and their description pushes nuclear theories to their limits. The most critical input parameter is the nuclear binding energy; a quantity that requires excellent measurement precision, since the two-neutron separation energy is small at the drip-line by definition. Moreover halo nuclides are typically very short-lived. Thus, a high accuracy instrument using a quick method of measurement is necessary. MISTRAL is such an instrument; it is a radiofrequency transmission mass spectrometer located at ISOLDE/CERN. In July 2003 we measured the mass of the Li11, a two-neutron halo nuclide. Our measurement improves the precision by a factor 6, with an error of 5 keV. Moreover the measurement gives a two-neutron separation energy 20% higher than the previous value. This measurement has an impact on the radius of the nucleus, and on the state of the two valence neutrons. At the same time, a measurement of the Be11 was performed with an uncertainty of 4 keV, in excellent agreement with previous measurements. In order to measure the mass of the two-neutron halo nuclide Be14, an ion beam cooling system is presently under development which will increase the sensitivity of the spectrometer. The second part of this work presents the development of this beam cooler using a gas-filled Paul trap. (author)

  5. Search for doubly-charged negative ions via accelerator mass spectrometry

    The Argonne FN tandem accelerator in conjunction with an Enge split-pole magnetic spectrograph has been used as a highly sensitive mass spectrometer to search for doubly charged negative ions of 11B, 12C and 16O. No evidence for the formation of these ions in an inverted sputter source and the subsequent acceleration in the tandem has been found. The following limits for the ratio of doubly-charged to singly-charged ions were measured: X--/X- -15, 11B; -15, 12C; -14, 16O. A relatively abundant formation of the short lived, metastable He- ion in the sputter source has been observed

  6. Large acceptance spectrometers for invariant mass spectroscopy of exotic nuclei and future developments

    Nakamura, T.; Kondo, Y.

    2016-06-01

    Large acceptance spectrometers at in-flight RI separators have played significant roles in investigating the structure of exotic nuclei. Such spectrometers are in particular useful for probing unbound states of exotic nuclei, using invariant mass spectroscopy with reactions at intermediate and high energies. We discuss here the key characteristic features of such spectrometers, by introducing the recently commissioned SAMURAI facility at the RIBF, RIKEN. We also investigate the issue of cross talk in the detection of multiple neutrons, which has become crucial for exploring further unbound states and nuclei beyond the neutron drip line. Finally we discuss future perspectives for large acceptance spectrometers at the new-generation RI-beam facilities.

  7. Continuation of Mass determinations through a Double Focusing Mass Spectrometer on Line with ISOLDE

    2002-01-01

    In a previous experiment (1976-77) we have demonstrated the interest and feasibility of atomic mass determinations from the direct measurements of mass ratios on Rb, Cs and Fr isotopes. Masses of long series of isotopes on both side of stability were determined with an accuracy of a few tens to 300 keV (for th exotic). Interesting nuclear structure features could be observed as for example the indication for an onset of deformation, at N~=~60 for Z~=~37, which stimulated further experiments and theoretical calculations. The many mass values, until then unknown, we obtained in our experiments, gave in addition the possibility to make detailed tests of the nuclear mass predictions. Due to improvements on our mass spectrometer (better transmission and higher resolving power) and increased ISOLDE production yields, some new and valuable measurements can be performed. We plan: \\item a) to continue the measurements towards even heavier isotopes and explore the deformation regions which start at |9|7Rb and |1|4|6Cs;...

  8. Characterization of a time-of-flight mass spectrometer and its applications in the study of solid surfaces; Charakterisierung eines Flugzeitmassenspektrometers und seine Anwendungen in der Festkoerperoberflaechenuntersuchung

    Mazarov, P.

    2006-12-21

    The object and the purpose of the present work was to develop, to assemble and to start running a new TOF (time of flight) mass spectrometer for imaging SNMS analytic which is optimized for the analysis of highly molecular secondary ions. The most important purpose was the characterization of the TOF mass spectrometer. The obtained mass spectra of indium, tantalum and silver clusters reflect the excellent properties of the TOF mass spectrometer for the detection of large clusters with good detection efficiency up to masses of 16000 amu. The possibility of the deflection of selected saturated atom and cluster peaks serves for further improvement of the detection efficiency for large molecules. The accessible mass resolution was determined to be of the order of m/{delta}m=1000 in the high mass region. Numerous measurements were carried out to characterize the useful yield of this spectrometer. For a best possible adaptation of the TOF mass spectrometer for the detection of highly molecular particles, a device for post-acceleration of the detected particles by up to 10 keV were inserted directly before the MCP detector. The detection efficiency of positive secondary ions was determined for different post-acceleration voltages for the example of sputtered indium cluster ions. In addition, a new method was developed for the quantitative determination of the spectral ionization probability {alpha}{sup +}({nu}) of sputtered particles as a function of the emission velocity. The next application of the TOF mass spectrometer is the analysis of complicated organic molecules in solid state surfaces. During measurements of the photo-ionization behaviour of neutral tryptophan molecules, it was found out that a stable molecular ion signal is generated in the SNMS spectrum with h{nu}=7.9 eV can only be observed by the use of a continuous ion beam or very long (ms range) ion pulses. (orig.)

  9. A statistical investigation of the mass discrepancy-acceleration relation

    Desmond, Harry

    2016-01-01

    We use the mass discrepancy-acceleration relation (the correlation between the ratio of dark-to-visible mass and acceleration in galaxies; MDAR) to test the galaxy-halo connection. We analyse the MDAR using a set of 14 statistics which quantify its four most important features: its shape, its scatter, the presence of a "characteristic acceleration scale," and the correlation of its residuals with other galaxy properties. We construct an empirical framework for the galaxy-halo connection in $\\...

  10. Indigenous realisation of measurement electronics for ion signal from mass spectrometer

    A PC based data measurement electronics has been realised for a Faraday cup detector signal. The Faraday cup detector serves as a complementary to a Daly detector of the thermal ionisation mass spectrometer. This report discusses about its indigenous development

  11. Development and Deployment of Retrofit PolarisQ Ion Trap Mass Spectrometer for Isotope Ratio Measurements

    This report describes Oak Ridge National Laboratory's (ORNL) FY15 progress in support of National Nuclear Security Administration's (NNSA) Portable Mass Spectrometer project. A retrofit PolarisQ ion trap mass spectrometer (RPMS) has been assembled from components of two PolarisQ ion trap mass spectrometers used in previous isotope ratio programs. The retrofit mass spectrometer includes a custom Hastelloy vacuum chamber which is about ¼ the size of the standard aluminum vacuum chamber and reduces the instrument weight from the original by nine pounds. In addition, the new vacuum chamber can be independently heated to reduce impurities such as water, which reacts with UF6 to produce HF in the vacuum chamber. The analyzer and all components requiring service are mounted on the chamber lid, facilitating quick and easy replacement of consumable components such as the filament and electron multiplier.

  12. Miniature Time of Flight Mass Spectrometer for Space and Extraterrestrial Applications Project

    National Aeronautics and Space Administration — The PI has developed a miniature time-of-flight mass spectrometer (TOF-MS), which can be op-timized for space and extraterrestrial applications, by using a...

  13. Development and Deployment of Retrofit PolarisQ Ion Trap Mass Spectrometer for Isotope Ratio Measurements

    Thompson, Cyril V. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Whitten, William B. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

    2015-11-01

    This report describes Oak Ridge National Laboratory’s (ORNL) FY15 progress in support of National Nuclear Security Administration’s (NNSA) Portable Mass Spectrometer project. A retrofit PolarisQ ion trap mass spectrometer (RPMS) has been assembled from components of two PolarisQ ion trap mass spectrometers used in previous isotope ratio programs. The retrofit mass spectrometer includes a custom Hastelloy vacuum chamber which is about ¼ the size of the standard aluminum vacuum chamber and reduces the instrument weight from the original by nine pounds. In addition, the new vacuum chamber can be independently heated to reduce impurities such as water, which reacts with UF6 to produce HF in the vacuum chamber. The analyzer and all components requiring service are mounted on the chamber lid, facilitating quick and easy replacement of consumable components such as the filament and electron multiplier.

  14. Automatic isotope ratio measurements with a double collector magnetic mass spectrometer

    This paper describes a measuring procedure and the instrumentation of automatic measurements of isotope ratios with double collector magnetic mass spectrometers. This is essentially achieved by discriminating the desired peak plateau for ion current integration during the high voltage variation. The resolution is nearly uneffected by offset drifts of the electronic system. Prior to every isotope ratio measurement the offset values are determined, digitally stored, and finally compensated when the isotope ratio is calculated with an arithmetic unit. Several mass spectrometers have been compared on the basis of an uranium isotope analysis in a long time experiment. The developed system proved reliable and showed the same resolution as more sophisticated spectrometer systems. (orig.)

  15. Double-arm time-of-flight mass-spectrometer of nuclear fragments

    A double-arm time-of-flight spectrometer of nuclear fragments for the investigation of heavy nuclei photofission in the intermediate energy range is described. The calibration results and working characteristics of the spectrometer, obtained using 252Cf as a source of spontaneous fission, are presented. A mass resolution of σ m ∼2-3 a.m.u. was obtained within the registered fragments mass range of 80-160 a.m.u. The spectrometer was tested in the experiment on the investigation of 238U nuclei fission by Bremsstahlung photons with Eγ max=1.75 GeV

  16. First direct mass measurements on nobelium and lawrencium with the Penning trap mass spectrometer SHIPTRAP

    The Penning trap mass spectrometer SHIPTRAP at GSI Darmstadt was set up for high-precision mass measurements of heavy radionuclides produced in fusion evaporation reactions and separated from the primary beam by the velocity filter SHIP. It consists of a gas stopping cell for the deceleration of the high energetic reaction products, an RFQ cooler and buncher for cooling and accumulation of the ions, and a double Penning trap system to perform mass measurements. The mass is determined by measuring the cyclotron frequency of the ion of interest in a strong homogeneous magnetic field and comparing it to the frequency of a well-known reference ion. With this method relative uncertainties in the order of 10-8 can be achieved. Recently, mass measurements of the three nobelium isotopes 252-254No (Z=102) and the lawrencium isotope 255Lr (Z=103) were performed successfully. These were the first direct mass measurements of transuranium elements ever per- formed. The production rate of the atoms of interest was about one per second or less. The results of the measurements on nobelium confirm the previous mass values which were deduced from Qα values. In the case of 255Lr the mass excess value, which was previously only estimated from systematic trends, was for the first time directly measured. These results mark the first step in the exploration of the region of transuranium elements which is planned at SHIPTRAP. The main objective is to fix the endpoints of α decay chains which are originating from superheavy elements close to the predicted island of stability. (orig.)

  17. First direct mass measurements on nobelium and lawrencium with the Penning trap mass spectrometer SHIPTRAP

    Dworschak, Michael Gerhard

    2009-12-08

    The Penning trap mass spectrometer SHIPTRAP at GSI Darmstadt was set up for high-precision mass measurements of heavy radionuclides produced in fusion evaporation reactions and separated from the primary beam by the velocity filter SHIP. It consists of a gas stopping cell for the deceleration of the high energetic reaction products, an RFQ cooler and buncher for cooling and accumulation of the ions, and a double Penning trap system to perform mass measurements. The mass is determined by measuring the cyclotron frequency of the ion of interest in a strong homogeneous magnetic field and comparing it to the frequency of a well-known reference ion. With this method relative uncertainties in the order of 10{sup -8} can be achieved. Recently, mass measurements of the three nobelium isotopes {sup 252-254}No (Z=102) and the lawrencium isotope {sup 255}Lr (Z=103) were performed successfully. These were the first direct mass measurements of transuranium elements ever per- formed. The production rate of the atoms of interest was about one per second or less. The results of the measurements on nobelium confirm the previous mass values which were deduced from Q{sub {alpha}} values. In the case of {sup 255}Lr the mass excess value, which was previously only estimated from systematic trends, was for the first time directly measured. These results mark the first step in the exploration of the region of transuranium elements which is planned at SHIPTRAP. The main objective is to fix the endpoints of {alpha} decay chains which are originating from superheavy elements close to the predicted island of stability. (orig.)

  18. High mass resolution time of flight mass spectrometer for measuring products in heterogeneous catalysis in highly sensitive microreactors

    Andersen, Thomas; Jensen, Robert; Christensen, M. K.;

    2012-01-01

    We demonstrate a combined microreactor and time of flight system for testing and characterization of heterogeneous catalysts with high resolution mass spectrometry and high sensitivity. Catalyst testing is performed in silicon-based microreactors which have high sensitivity and fast thermal...... response. Gas analysis is performed with a time of flight mass spectrometer with a modified nude Bayard-Alpert ionization gauge as gas ionization source. The mass resolution of the time of flight mass spectrometer using the ion gauge as ionization source is estimated to m∕Δm > 2500. The system design...

  19. Radio-tracing 'without' radioactivity: accelerator mass spectrometry in biomedicine

    Accelerator mass spectrometry (AMS) is a form of isotope-ratio mass spectrometry that quantifies concentrations of certain long-lived radioisotopes independently of their radioactive decay. AMS is primarily used in the geosciences for determining the age of a material that contains naturally occurring radioisotopes. AMS uses the same high specificity for enriched levels of these radioisotopes in tracing low chemical doses for long periods in biological systems, including humans. AMS provides the safety of low radiative exposure to experimental subjects and investigators, while obtaining attomole sensitivities that are not possible with stable isotope tracers because of their natural isotopic abundances. AMS isotope tracing was first applied to quantifying the genotoxicity of low level environmental chemicals in animals and later in humans. Physiologic concentrations of 14C-labeled trace nutrients (folate, carotene, and tocopherol) are now measured directly in humans without concern about radiation. The radiative exposure is less than the commonly accepted risks of natural background radiation or the radiation fields found in high altitude air flights. AMS measures very small biological samples (such as 20 microliters of blood) that are easily obtained from human volunteers or model animals at frequent intervals for detailed analysis of kinetic profiles. This high data density enables the construction of compartmental models that elucidate nutrient behavior in tissues that cannot be directly sampled. The pharmaceutical industry is enthusiastic about AMS as a detector for 'micro-dosing' in which the human kinetics of an assuredly non-toxic dose of a candidate drug is tested early in a development project. Molecular tracing uses 3H or 14C as common isotopic labels, but AMS contributes to elemental tracing with certain radioisotopes having very long lives, such as 26AL or 41Ca. Calcium-41 is a particularly useful isotope in biomedical research because it is used to

  20. A novel high-capacity ion trap-quadrupole tandem mass spectrometer

    Krutchinsky, Andrew N.; Cohen, Herbert; Chait, Brian T.

    2007-12-01

    We describe a prototype tandem mass spectrometer that is designed to increase the efficiency of linked-scan analyses by >100-fold over conventional linked-scan instruments. The key element of the mass spectrometer is a novel high ion capacity ion trap, combined in tandem configuration with a quadrupole collision cell and a quadrupole mass analyzer (i.e. a TrapqQ configuration). This ion trap can store >106 ions without significant degradation of its performance. The current mass resolution of the trap is 100-450 full width at half maximum for ions in the range 800-4000 m/z, yielding a 10-20 m/z selection window for ions ejected at any given time into the collision cell. The sensitivity of the mass spectrometer for detecting peptides is in the low femtomole range. We can envisage relatively straightforward modifications to the instrument that should improve both its resolution and sensitivity. We tested the tandem mass spectrometer for collecting precursor ion spectra of all the ions stored in the trap and demonstrated that we can selectively detect a phosphopeptide in a mixture of non-phosphorylated peptides. Based on this prototype instrument, we plan to construct a fully functional model of the mass spectrometer for detecting modification sites on proteins and profiling their abundances with high speed and sensitivity.

  1. Mass Spectrometric Analysis of Eight Common Chemical Explosives Using Ion Trap Mass Spectrometer

    Park, Sehwan; Lee, Jihyeon; KIm, Jeongkwon [Chungnam National Univ., Daejeon (Korea, Republic of); Cho, Soo Gyeong; Goh, Eun Mee [Agency for Defense Development, Daejeon (Korea, Republic of); Lee, Sungman; Koh, Sungsuk [Sensor Tech Inc., Seoul (Korea, Republic of)

    2013-12-15

    Eight representative explosives (ammonium perchlorate (AP), ammonium nitrate (AN), trinitrotoluene (TNT), 2,4-dinitrotoluene (DNT), cyclonite (RDX), cyclotetramethylenetetranitramine (HMX), pentaerythritol tetranitrate (PETN), and hexanitrostilbene (HNS)) were comprehensively analyzed with an ion trap mass spectrometer in negative ion mode using direct infusion electrospray ionization. MS/MS experiments were performed to generate fragment ions from the major parent ion of each explosive. Explosives in salt forms such as AP or AN provided cluster parent ions with their own anions. Explosives with an aromatic ring were observed as either [M.H]{sup -} for TNT and DNT or [M]{sup ·-}. for HNS, while explosives without an aromatic ring such as RDX, HMX, and PETN were detected as an adduct ion with a formate anion, i. e., [M+HCOO]{sup -}. These findings provide a guideline for the rapid and accurate detection of explosives once portable MS instruments become more readily available.

  2. Mass Spectrometric Analysis of Eight Common Chemical Explosives Using Ion Trap Mass Spectrometer

    Eight representative explosives (ammonium perchlorate (AP), ammonium nitrate (AN), trinitrotoluene (TNT), 2,4-dinitrotoluene (DNT), cyclonite (RDX), cyclotetramethylenetetranitramine (HMX), pentaerythritol tetranitrate (PETN), and hexanitrostilbene (HNS)) were comprehensively analyzed with an ion trap mass spectrometer in negative ion mode using direct infusion electrospray ionization. MS/MS experiments were performed to generate fragment ions from the major parent ion of each explosive. Explosives in salt forms such as AP or AN provided cluster parent ions with their own anions. Explosives with an aromatic ring were observed as either [M.H]- for TNT and DNT or [M]·-. for HNS, while explosives without an aromatic ring such as RDX, HMX, and PETN were detected as an adduct ion with a formate anion, i. e., [M+HCOO]-. These findings provide a guideline for the rapid and accurate detection of explosives once portable MS instruments become more readily available

  3. Compact Ion and Neutral Mass Spectrometer with Ion Drifts, Temperatures and Neutral Winds

    Paschalidis, Nikolaos

    2016-07-01

    In situ measurements of atmospheric neutral and ion composition and density, temperatures, ion drifts and neutral winds, are in high demand to study the dynamics of the ionosphere-theremosphere-mesosphere system. This paper presents a compact Ion and Neutral Mass Spectrometer (INMS) with impended ion drifts and temperature, and neutral winds capability for in situ measurements of ions and neutrals H, He, N, O, N2, O2. The mass resolution M/dM is approximately 10 at an incoming energy range of 0-20eV. The goal is to resolve ion drifts in the range 0 to 3000m/sec with a resolution better than 50m/sec, and neutral winds in the range of 0 to 1000m/sec with similar resolution. For temperatures the goal is to cover a dynamic range of 0 to 5000K. The INMS is based on front end optics for ions and neutrals, pre acceleration, gated time of flight, top hat ESA, MCP detectors and compact electronics. The instrument is redundant for ions and neutrals with the ion and neutral sensor heads on opposite sides and with full electronics in the middle. The ion front end includes RPA for temperature scanning and neutral front end includes angular modulation and thermionic ionization and ion blocking grids. The electronics include fast electric gating, TOF electronics, TOF binning and C&DH digital electronics. The data package includes 400 mass bins each for ions and neutrals and key housekeeping data for instrument health and calibration. The data sampling can be commanded from 0.1 to 10 sec with 1sec nominal setting. The instrument has significant onboard storage capability and a data compression scheme. The mass spectrometer version of the instrument has been flown on the Exocube mission. The instrument occupied 1.5U volume, weighed only 560 g and required nominal power of 1.6W The ExoCube mission was designed to acquire global knowledge of in-situ densities of [H], [He], [O] and H+, He+, O+ in the upper ionosphere and lower exosphere in combination with incoherent scatter radar and

  4. Electronics for processing of data from a double collector isotopic ratio mass spectrometer

    The output data available from the mass spectrometer type MS-660 developed in the mass spectrometry section of Technical Physics Division of the Bhabha Atomic Research Centre, Bombay, for the determination of H/D ratios in liquid/gas sample consist of uncompensated mass 3 and mass 2 signals. After the mass 3 signal has been compensated for H3+ formation, the on-line ratio of compensated mass 3 to mass 2 is calculated, displayed, and then printed on a printer for record. The electronic compensation circuit, the discrete voltage-to-frequency (V/F) converter circuit, the ratio calculating system using V/F converters, and a digital interface system for Hindustan Teleprinter to print out the ratios are explained. Results obtained on mass spectrometer MS-660 are presented. (auth.)

  5. High-throughput mass-directed parallel purification incorporating a multiplexed single quadrupole mass spectrometer.

    Xu, Rongda; Wang, Tao; Isbell, John; Cai, Zhe; Sykes, Christopher; Brailsford, Andrew; Kassel, Daniel B

    2002-07-01

    We report on the development of a parallel HPLC/MS purification system incorporating an indexed (i.e., multiplexed) ion source. In the method described, each of the flow streams from a parallel array of HPLC columns is directed toward the multiplexed (MUX) ion source and sampled in a time-dependent, parallel manner. A visual basic application has been developed and monitors in real-time the extracted ion current from each sprayer channel. Mass-directed fraction collection is initiated into a parallel array of fraction collectors specific for each of the spray channels. In the first embodiment of this technique, we report on a four-column semipreparative parallel LC/MS system incorporating MUX detection. In this parallel LC/MS application (in which sample loads between 1 and 10 mg on-column are typically made), no cross talk was observed. Ion signals from each of the channels were found reproducible over 192 injections, with interchannel signal variations between 11 and 17%. The visual basic fraction collection application permits preset individual start collection and end collection thresholds for each channel, thereby compensating for the slight variation in signal between sprayers. By incorporating postfraction collector UV detection, we have been able to optimize the valve-triggering delay time with precut transfer tubing between the mass spectrometer and fraction collectors and achieve recoveries greater than 80%. Examples of the MUX-guided, mass-directed fraction purification of both standards and real library reaction mixtures are presented within. PMID:12141664

  6. Analysis of isotopic ratio 235U/238U of UF6 with quadrupole mass spectrometer

    The uranium enrichment assay is vital to the research and development of uranium enrichment technology. In order to develop a small, light and high speed mass scanning quadrupole mass spectrometer as an on-line mass spectrometer, the design and trial fabrication of the system have been carried out, together with various performance evaluation tests. For the system, it is desirable to select the structure capable of making the preliminary experiments for on-line assay. The essential conditions for the uranium enrichment assay include enough resolution to identify uranium isotopes; good accuracy and precision; and small memory effect. The mass spectrometer fabricated for trial was confirmed to nearly satisfy these requirements. Residual UF6 in the ionization chamber reaches 1/50,000 in three minutes after evacuation, so that the memory effect is negligible. The necessary conditions for the on-line assay include the stable operation of the system for long time and small consumption of UF6. The measurement of reproducibility of isotopic ratio was made by introducing UF6 continuously and operating the system for long time. While the quadrupole mass spectrometer fabricated for trial was judged to be applicable to uranium enrichment test, the applicability as an on-line mass spectrometer will be evaluated in the field test of the cascade in future. (Kobatake, H.)

  7. The development of accelerator mass spectroscopy system

    Mitarai, Shiro; Machida, Atsushi; Iwata, Yasunao; Tsubusaki, Yoshihiro; Tanaka, Katsuhiko; Maeda, Toyokazu; Nakajima, Takao [Kyushu Univ., Fukuoka (Japan)

    2001-02-01

    Inverse PIXE method was applied to the differentiation of Chlorine 36 and Sulfur 36. The contaminated soil from the USSR nuclear test site was measured. Terminal potential of the tandem accelerator was controlled by GVM. A new AMS system, using time-of flight method is under development. The development of beam buncher and beam chopper for the system is briefly described. (A. Yamamoto)

  8. A computer controlled mass spectrometer system for investigating the decomposition of non-metallic materials under atmospheric conditions

    Thompson, J. M.

    1985-01-01

    A PDP 11/23 quadrupole mass spectrometer system was coupled to a nondiscriminating gas inlet system permitting gases at atmospheric pressure to be admitted into a high vacuum chamber containing the ion source of the mass spectrometer without separation of the gaseous components. The resolution of related software problems has resulted in a convenient computer-mass spectrometer system capable of generating masses, relative intensities and related data on the gaseous products resulting from the atmospheric thermal decomposition of nonmetallic materials.

  9. Hybrid micropixel detector at the focal plane of the mass-spectrometer

    Results on testing TimePix micropixel chip as a detector of low energy ions in a focal plane of the laser mass-spectrometer are presented. Two options were tested: hybrid micro-pixel detector as well as metal micro-pixel detector (naked read-out chip with a metal mesh to improve a charge collection). For both cases a response uniformity of pixels over ion mass, energy and detection position has been thoroughly studied. The results obtained illustrate capability of both detector modes to be used for creating 'electronic focal plane' of a mass-spectrometer with obvious advantages of real time devices.

  10. A GPU Accelerated Spring Mass System for Surgical Simulation

    Mosegaard, Jesper; Sørensen, Thomas Sangild

    2005-01-01

    There is a growing demand for surgical simulators to dofast and precise calculations of tissue deformation to simulateincreasingly complex morphology in real-time. Unfortunately, evenfast spring-mass based systems have slow convergence rates for largemodels. This paper presents a method to accele...... accelerate computation of aspring-mass system in order to simulate a complex organ such as theheart. This acceleration is achieved by taking advantage of moderngraphics processing units (GPU)....

  11. Mass resolution of accelerated ions in LNR cyclotrons

    The possibiliti of separating in cyclotron accelerated ions with different mass-to-charge ratios is considered. The calculations and experiment have demonstrated that mass resolution of accelerated ions for the U-400 cyclotron is approximately 3600; for U-200 cyclotron, approximately 1500. Ion beams which have not been separated in the cyclotron may be separated during beam extraction by means of the charge exchange in thin targets

  12. Studies on reducing the scale of a double focusing mass spectrometer

    Several groups have developed miniaturized sector mass spectrometers with the goal of remote sensing in confined spaces or portability. However, these achievements have been overshadowed by more successful development of man-portable quadrupole and ion trap mass spectrometers. Despite these accomplishments the development of a reduced-scale sector mass spectrometer remains attractive as a potentially low-cost, robust instrument requiring very simple electronics and low power. Previous studies on miniaturizing sector instruments include the use of a Mattauch-Herzog design for a portable mass spectrograph weighing less than 10 kg. Other work has included the use of a Nier-Johnson design in spacecraft-mountable gas chromatography mass spectrometers for the Viking spacecraft as well as miniature sector-based MS/MS instrument. Although theory for designing an optimized system with high resolution and mass accuracy is well understood, such specifications have not yet been achieved in a miniaturized instrument. To proceed further toward the development of a miniaturized sector mass spectrometer, experiments were conducted to understand and optimize a practical, yet nonideal instrument configuration. The sector mass spectrometer studied in this work is similar to the ones developed for the Viking project, but was further modified to be low cost, simple and robust. Characteristics of this instrument that highlight its simplicity include the use of a modified Varian leak detector ion source, source ion optics that use one extraction voltage, and an unshunted fixed nonhomogeneous magnetic sector. The effects of these design simplifications on ion trajectory were studied by manipulating the ion beam along with the magnetic sector position. This latter feature served as an aid to study ion focusing amidst fringing fields as well as nonhomogeneous forces and permitted empirical realignment of the instrument

  13. Time-of-flight mass spectrometer for fullerene and recoil ions: design and construction

    the machining of most components. The entire mass spectrometer will be mounted on a support to rise the mass spectrometer mean plane to the level of the accelerated particle beam. (authors)

  14. Mass separation of deuterium and helium with conventional quadrupole mass spectrometer by using varied ionization energy

    Yu, Yaowei; Hu, Jiansheng; Wan, Zhao; Wu, Jinhua; Wang, Houyin; Cao, Bin

    2016-03-01

    Deuterium pressure in deuterium-helium mixture gas is successfully measured by a common quadrupole mass spectrometer (model: RGA200) with a resolution of ˜0.5 atomic mass unit (AMU), by using varied ionization energy together with new developed software and dedicated calibration for RGA200. The new software is developed by using MATLAB with the new functions: electron energy (EE) scanning, deuterium partial pressure measurement, and automatic data saving. RGA200 with new software is calibrated in pure deuterium and pure helium 1.0 × 10-6-5.0 × 10-2 Pa, and the relation between pressure and ion current of AMU4 under EE = 25 eV and EE = 70 eV is obtained. From the calibration result and RGA200 scanning with varied ionization energy in deuterium and helium mixture gas, both deuterium partial pressures (PD2) and helium partial pressure (PHe) could be obtained. The result shows that deuterium partial pressure could be measured if PD2 > 10-6 Pa (limited by ultimate pressure of calibration vessel), and helium pressure could be measured only if PHe/PD2 > 0.45, and the measurement error is evaluated as 15%. This method is successfully employed in EAST 2015 summer campaign to monitor deuterium outgassing/desorption during helium discharge cleaning.

  15. Mass separation of deuterium and helium with conventional quadrupole mass spectrometer by using varied ionization energy.

    Yu, Yaowei; Hu, Jiansheng; Wan, Zhao; Wu, Jinhua; Wang, Houyin; Cao, Bin

    2016-03-01

    Deuterium pressure in deuterium-helium mixture gas is successfully measured by a common quadrupole mass spectrometer (model: RGA200) with a resolution of ∼0.5 atomic mass unit (AMU), by using varied ionization energy together with new developed software and dedicated calibration for RGA200. The new software is developed by using MATLAB with the new functions: electron energy (EE) scanning, deuterium partial pressure measurement, and automatic data saving. RGA200 with new software is calibrated in pure deuterium and pure helium 1.0 × 10(-6)-5.0 × 10(-2) Pa, and the relation between pressure and ion current of AMU4 under EE = 25 eV and EE = 70 eV is obtained. From the calibration result and RGA200 scanning with varied ionization energy in deuterium and helium mixture gas, both deuterium partial pressures (PD2 ) and helium partial pressure (PHe) could be obtained. The result shows that deuterium partial pressure could be measured if PD2 > 10(-6) Pa (limited by ultimate pressure of calibration vessel), and helium pressure could be measured only if PHe/PD2 > 0.45, and the measurement error is evaluated as 15%. This method is successfully employed in EAST 2015 summer campaign to monitor deuterium outgassing/desorption during helium discharge cleaning. PMID:27036832

  16. Size-exclusion chromatography with organic carbon detection using a mass spectrometer.

    Warton, Ben; Heitz, Anna; Allpike, Bradley; Kagi, Robert

    2008-10-17

    A novel organic carbon detector for size-exclusion chromatography (SEC) is described. The instrument uses the conventional UV-persulfate oxidation method to convert organic carbon to CO(2), which is then detected using a mass spectrometer. This system, using the mass spectrometer, had lower limits of detection (LOD) and limits of quantification (LOQ) than a previously described system using a Fourier transform infrared (FTIR) spectroscopy 'lightpipe' detector (i.e. when quantification was based on calibration using phthalate standards). When used to analyse natural organic matter (NOM) in water, it also had a superior signal-to-noise ratio to the previously described system. The use of a mass spectrometer to detect organic carbon (as CO(2)) enables the possibility of further characterisation of NOM by measuring the stable carbon isotope ratios of the various molecular size fractions of organic carbon, as obtained by SEC. PMID:18790486

  17. The analysis of uranium in environmental sample by mass spectrometer combined with isotopic dilution

    Uranium in the environmental sample was analyzed by mass spectrometer combined with isotopic dilution. Before mass spectrometer analysis, samples were dissolved in a concentrated acidic solution containing HNO3, HF and HClO4 and chemically processed to suit the analysis requirement. Analysis results indicated that the uranium content was 0.08 μg/g in river water, 0.1 μg/g in evergreen foliage, and 5-11 μg/g in surface soil respectively. (authors)

  18. Fabrication and testing of recoil mass spectrometer at Mumbai Pelletron

    The main motivation for the recoil mass separator, which has been designed and constructed at the Mumbai Pelletron, has been to study the exotic nuclei far off from the line of β-stability, produced through fusion-evaporation reactions. These have very low cross sections, of the order of a few microbarns and the reaction products recoil in the forward direction along with the beam particles. The recoil mass separator enables one to study these reaction products by separating them from the main beam and from each other

  19. Study of Odor Approximation by Using Mass Spectrometer

    Ohno, Masashi; Nihei, Yasunori; Nakamoto, Takamichi

    2011-09-01

    Since a set of odor components to cover wide range of smells has not been revealed yet, we studied the selection of odor components using essential-oil mass spectrum database. Basis vectors were extracted using non-negative matrix factorization method1 and then non-negative least squares method was used to determine the recipe. The odor approximations of three typical essential oils were confirmed by the sensory test. It was found that the mass spectrum data were correlated with the sensory test result. Moreover, this correlation was remarkable in the high m/z region.

  20. Accelerator mass spectrometry in biomedical research

    Vogel, J.S.; Turteltaub, K.W.

    1993-10-20

    Biological effects occur in natural systems at chemical concentrations of parts per billion (1:10{sup 9}) or less. Affected biomolecules may be separable in only milligram or microgram quantities. Quantification at attomole sensitivity is needed to study these interactions. AMS measures isotope concentrations to parts per 10{sup 13--15} on milligram-sized samples and is ideal for quantifying long-lived radioisotopic labels that are commonly used to trace biochemical pathways in natural systems. {sup 14}C-AMS has now been coupled to a variety of organic separation and definition technologies. The primary research investigates pharmacokinetics and genotoxicities of toxins and drugs at very low doses. Human subject research using AMS includes nutrition, toxicity and elemental balance studies. {sup 3} H, {sup 41}Ca and {sup 26}Al are also traced by AMS for fundamental biochemical kinetic research. Expansion of biomedical AMS awaits further development of biochemical and accelerator technologies designed specifically for these applications.

  1. Accelerator mass spectrometry in biomedical research

    Biological effects occur in natural systems at chemical concentrations of parts per billion (1:109) or less. Affected biomolecules may be separable in only milligram or microgram quantities. Quantification at attomole sensitivity is needed to study these interactions. AMS measures isotope concentrations to parts per 1013--15 on milligram-sized samples and is ideal for quantifying long-lived radioisotopic labels that are commonly used to trace biochemical pathways in natural systems. 14C-AMS has now been coupled to a variety of organic separation and definition technologies. The primary research investigates pharmacokinetics and genotoxicities of toxins and drugs at very low doses. Human subject research using AMS includes nutrition, toxicity and elemental balance studies. 3 H, 41Ca and 26Al are also traced by AMS for fundamental biochemical kinetic research. Expansion of biomedical AMS awaits further development of biochemical and accelerator technologies designed specifically for these applications

  2. High Energy Collisions on Tandem Time-of-Flight Mass Spectrometers

    Cotter, Robert J.

    2013-05-01

    Long before the introduction of matrix-assisted laser desorption/ionization (MALDI), electrospray ionization (ESI), Orbitraps, and any of the other tools that are now used ubiquitously for proteomics and metabolomics, the highest performance mass spectrometers were sector instruments, providing high resolution mass measurements by combining an electrostatic energy analyzer (E) with a high field magnet (B). In its heyday, the four sector mass spectrometer (or EBEB) was the crown jewel, providing the highest performance tandem mass spectrometry using single, high energy collisions to induce fragmentation. During a time in which quadrupole and tandem triple quadrupole instruments were also enjoying increased usage and popularity, there were, nonetheless, some clear advantages for sectors over their low collision energy counterparts. Time-of-flight (TOF) mass spectrometers are high voltage, high vacuum instruments that have much in common with sectors and have inspired the development of tandem instruments exploiting single high energy collisions. In this retrospective, we recount our own journey to produce high performance TOFs and tandem TOFs, describing the basic theory, problems, and the advantages for such instruments. An experiment testing impulse collision theory (ICT) underscores the similarities with sector mass spectrometers where this concept was first developed. Applications provide examples of more extensive fragmentation, side chain cleavages, and charge-remote fragmentation, also characteristic of high energy sector mass spectrometers. Moreover, the so-called curved-field reflectron has enabled the design of instruments that are simpler, collect and focus all of the ions, and may provide the future technology for the clinic, for tissue imaging, and the characterization of microorganisms.

  3. Mass spectrometer for real-time metabolism monitoring during anesthesia

    Elizarov, A. Yu.; Levshankov, A. I.

    2012-06-01

    Mass-spectrometric monitoring of metabolism (CO2/O2) in the inspiration-expiration regime is used to estimate the anesthetic protection of the patient against surgical stimulation during combined anesthesia. A correlation between the anesthetic protection of the patient and the metabolic rate is demonstrated, and the periodic variation of the metabolic rate with time is found. The sevoflurane metabolism products and intravenous analgesic fentanyl are found in the blowing air of the patient during anesthesia.

  4. Method for selective detection of explosives in mass spectrometer or ion mobility spectrometer at parts-per-quadrillion level

    Ewing, Robert G.; Atkinson, David A.; Clowers, Brian H.

    2015-09-01

    A method for selective detection of volatile and non-volatile explosives in a mass spectrometer or ion mobility spectrometer at a parts-per-quadrillion level without preconcentration is disclosed. The method comprises the steps of ionizing a carrier gas with an ionization source to form reactant ions or reactant adduct ions comprising nitrate ions (NO.sub.3.sup.-); selectively reacting the reactant ions or reactant adduct ions with at least one volatile or non-volatile explosive analyte at a carrier gas pressure of at least about 100 Ton in a reaction region disposed between the ionization source and an ion detector, the reaction region having a length which provides a residence time (tr) for reactant ions therein of at least about 0.10 seconds, wherein the selective reaction yields product ions comprising reactant ions or reactant adduct ions that are selectively bound to the at least one explosive analyte when present therein; and detecting product ions with the ion detector to determine presence or absence of the at least one explosive analyte.

  5. Accelerator-mass spectroscopy with fully stripped 36Cl

    The Garching MP tandem-post accelerator-achromator accelerator facility was extended in such way that by it a very backgroundless accelerator mass spectroscopy with fully stripped medium heavy ions was possible. As first applications microscopical amounts of 36Cl (Tsub(1/2)= 301 000 years) were detected. The detection limit lies at 36Cl/CL=4x10-15. In first measurements the method was applied to the age determination of palaeontological samples and to the study of cosmic-radiation induced reactions in the earth crust. (orig.)

  6. Performance results of a mobile high-resolution MR-TOF mass spectrometer for in-situ analytical mass spectrometry

    Lippert, Wayne; Lang, Johannes [Justus-Liebig-Universitaet Giessen (Germany); Ayet San Andres, Samuel [GSI, Darmstadt (Germany); Dickel, Timo; Geissel, Hans; Plass, Wolfgang; Scheidenberger, Christoph [Justus-Liebig-Universitaet Giessen (Germany); GSI, Darmstadt (Germany); Yavor, Mikhail [RAS St. Petersburg (Russian Federation)

    2014-07-01

    A mobile multiple-reflection time-of-flight mass spectrometer (MR-TOF-MS) has been developed which provides a mass resolving power exceeding 250,000 and sub-ppm mass accuracy in a transportable format. Thus it allows resolving isobars and enables accurate determination of the composition and structure of biomolecules. Furthermore the device offers high mass resolving MS/MS capability via selective ion re-trapping and collisional-induced dissociation (CID). An atmospheric pressure interface (API) provides for routine measurements with various atmospheric ion sources. All supply electronics, DAQ and control system are mounted with the spectrometer into a single frame with a total volume of only 0.8 m{sup 3}. With the current system many applications like waste water monitoring at hot spots, mass-based classification of biomolecules and breath analysis are possible. In addition the mass spectrometer is readily scalable and can be adopted and simplified for even more specific use like in space science for instance. A characterization and first performance results are shown, and the implementation of MS/MS in combination with CID is discussed.

  7. Performance results of a mobile high-resolution MR-TOF mass spectrometer for in-situ analytical mass spectrometry

    A mobile multiple-reflection time-of-flight mass spectrometer (MR-TOF-MS) has been developed which provides a mass resolving power exceeding 250,000 and sub-ppm mass accuracy in a transportable format. Thus it allows resolving isobars and enables accurate determination of the composition and structure of biomolecules. Furthermore the device offers high mass resolving MS/MS capability via selective ion re-trapping and collisional-induced dissociation (CID). An atmospheric pressure interface (API) provides for routine measurements with various atmospheric ion sources. All supply electronics, DAQ and control system are mounted with the spectrometer into a single frame with a total volume of only 0.8 m3. With the current system many applications like waste water monitoring at hot spots, mass-based classification of biomolecules and breath analysis are possible. In addition the mass spectrometer is readily scalable and can be adopted and simplified for even more specific use like in space science for instance. A characterization and first performance results are shown, and the implementation of MS/MS in combination with CID is discussed.

  8. Potentiality evaluation of the MAT 250 UF mass spectrometer for general analysis

    This work presents a study on the potentiality of the MAT 250 UF mass spectrometer. It was formerly used only, for uranium isotopic analysis. It will be used, flow now on, also for the analysis of other gases such as deuterium, helium and hydrogen, as well. (A.C.A.S.)

  9. Desorption electrospray ionization with a portable mass spectrometer: in situ analysis of ambient surfaces.

    Mulligan, Christopher C; Talaty, Nari; Cooks, R Graham

    2006-04-28

    Desorption electrospray ionization (DESI) is implemented on a portable mass spectrometer and used to demonstrate in situ detection of active ingredients in pharmaceutical preparations, alkaloids in plant tissues, explosives, chemical warfare agent simulants and agricultural chemicals from a variety of surfaces; air monitoring applications using DESI are also introduced. PMID:16609779

  10. High resolution (GC/MS) mass spectrometer data acquisition and processing system based on microcomputer

    A high resolution (GC/MS) mass spectrometer data acquisition and processing system based on IBM-PC/AT is introduced in this paper. Its hardware design and system software are described simply, and a comparison between two measurement results on standard samples PFK obtained with this system and minicomputer is given

  11. MEMS Fabrication of Micro Cylindrical Ion Trap Mass Spectrometer for CubeSats Application

    Zheng, Y.

    2015-10-01

    Microelectromechanical Systems (MEMS) technology is used to fabricate arrays of micro Cylindrical Ion Traps (μCIT) which are integrated into a miniaturized mass spectrometer (MS). The micro μCITs are built from silicon wafers and requires high machining precision, smooth surface, and high dimensional uniformity across the array for optimum mass spectrometer performance. In order to build these 3D miniature structures several MEMS processing techniques were explored and a process was developed and tested. By using the developed MEMS process, the required μCIT 4 x 4 arrays were fabricated. This included a chip design variation in which mechanical locking pits and posts were machined in the Ring Electrode (RE) chip and End Plate (EP) chips respectively, for self-assembly. The size of the assembled μCIT is only 12 mm x 12 mm x 1.5 mm. It is a key component for the miniature mass spectrometer. The micro cylindrical ion trap mass spectrometer has the advantages of low-power operation, simpler electronics and less-stringent vacuum system requirements. The MEMS batch production capabilities will also greatly lower the cost. It is a promising candidate for CubeSat and nanoSats applications for exploration of chemical distributions in space.

  12. Development of a high vacuum sample preparation system for helium mass spectrometer

    A high vacuum sample preparation system for the 3He/4He ratio mass spectrometer (Helix SFT) has been developed to remove all the gaseous constituents excluding helium from the field gases. The sample preparation system comprises of turbo molecular pump, ion pump, zirconium getter, pipettes and vacuum gauges with controller. All these are fitted with cylindrical SS chamber using all metal valves. The field samples are initially treated with activated charcoal trap immersed in liquid nitrogen to cutoff major impurities and moisture present in the sample gas. A sample of 5 ml is collected out of this stage at a pressure of 10−2 mbar. This sample is subsequently purified at a reduced pressure of 10−7 mbar before it is injected into the ion source of the mass spectrometer. The sample pressure was maintained below 10−7 mbar with turbo molecular vacuum pumps and ion pumps. The sample gas passes through several getter elements and a cold finger with the help of manual high vacuum valves before it is fed to the mass spectrometer. Thus the high vacuum sample preparation system introduces completely clean, dry and refined helium sample to the mass spectrometer for best possible analysis of isotopic ratio of helium.

  13. Acquisition systems and data elaboration for Varian Mat 1129 mass spectrometers

    The data acquisition equipment to be described is used to capture data deriving from the Varian Mat 1125 mass spectrometer. It is based on a system controlled by the microprocessor 8085 and was designed with the aim of advantegeously replacing the photosensitive paper recorder used originally. (Author)

  14. Ultrasensitive resonance ionization mass spectrometer for evaluating krypton contamination in xenon dark matter detectors

    An ultrasensitive resonance ionization mass spectrometer that can be applied to evaluate krypton (Kr) contamination in xenon (Xe) dark matter detectors has been developed for measuring Kr at the parts-per-trillion (ppt) or sub-ppt level in Xe. The gas sample is introduced without any condensation into a time-of-flight mass spectrometer through a pulsed supersonic valve. Using a nanosecond pulsed laser at 212.6 nm, 84Kr atoms in the sample are resonantly ionized along with other Kr isotopes. 84Kr ions are then mass separated and detected by the mass spectrometer in order to measure the Kr impurity concentration. With our current setup, approximately 0.4 ppt of Kr impurities contained in pure argon (Ar) gas are detectable with a measurement time of 1000 s. Although Kr detection sensitivity in Xe is expected to be approximately half of that in Ar, our spectrometer can evaluate Kr contamination in Xe to the sub-ppt level

  15. Frequency-swept detector for ion cyclotron resonance mass spectrometers

    Wronka, J.; Ridge, D. P.

    1982-04-01

    Design, construction, performance, and use of a frequency-swept bridge detector for ion cyclotron resonance mass spectrometry are described. Special features include characterization and simple automatic correction of phase shift to allow broadband detection. The result is a detection system that may be used either at constant field or constant frequency. Drift-mode operation is simplified in that it may be satisfactorily used without the various signal modulation schemes used in previous detectors. In the trapped mode the detector may be pulsed to control the timing of ion detection. This detector makes it possible to do frequency-swept double resonance experiments which provide spectra of all the product ions of a given reactant ion. Circuit schematics and typical frequency- and field-swept spectra are shown.

  16. HD gas analysis with Gas Chromatography and Quadrupole Mass Spectrometer

    Ohta, T; Didelez, J -P; Fujiwara, M; Fukuda, K; Kohri, H; Kunimatsu, T; Morisaki, C; Ono, S; Rouille, G; Tanaka, M; Ueda, K; Uraki, M; Utsuro, M; Wang, S Y; Yosoi, M

    2011-01-01

    A gas analyzer system has been developed to analyze Hydrogen-Deuteride (HD) gas for producing frozen-spin polarized HD targets, which are used for hadron photoproduction experiments at SPring-8. Small amounts of ortho-H$_{2}$ and para-D$_{2}$ gas mixtures ($\\sim$0.01%) in the purified HD gas are a key to realize a frozen-spin polarized target. In order to obtain reliable concentrations of these gas mixtures in the HD gas, we produced a new gas analyzer system combining two independent measurements with the gas chromatography and the QMS. The para-H$_{2}$, ortho-H$_{2}$, HD, and D$_{2}$ are separated using the retention time of the gas chromatography and the mass/charge. It is found that the new gas analyzer system can measure small concentrations of $\\sim$0.01% for the otho-H$_2$ and D$_2$ with good S/N ratios.

  17. Development of a GC/Quadrupole-Orbitrap Mass Spectrometer, Part II: New Approaches for Discovery Metabolomics

    Peterson, Amelia C.; Balloon, Allison J.; Westphall, Michael S.; Coon, Joshua J.

    2014-01-01

    Identification of unknown peaks in gas chromatography/mass spectrometry (GC/MS)-based discovery metabolomics is challenging, and remains necessary to permit discovery of novel or unexpected metabolites that may elucidate disease processes and/or further our understanding of how genotypes relate to phenotypes. Here, we introduce two new technologies and an analytical workflow that can facilitate the identification of unknown peaks. First, we report on a GC/Quadrupole-Orbitrap mass spectrometer...

  18. Design of Portable Mass Spectrometers with Handheld Probes: Aspects of the Sampling and Miniature Pumping Systems

    Chen, Chien-Hsun; Chen, Tsung-Chi; Zhou, Xiaoyu; Kline-Schoder, Robert; Sorensen, Paul; Cooks, R. Graham; Ouyang, Zheng

    2014-01-01

    Miniature mass spectrometry analytical systems of backpack configuration fitted with sampling probes could potentially be of significant interest for in-field, real-time chemical analysis. In this study, various configurations were explored in which a long narrow tube was used to connect the turbo and backing pumps used to create and maintain vacuum. Also, for the first time we introduced two new types of pumps for miniature mass spectrometers, the Creare 130g drag pump and Creare 350g scroll...

  19. On-line monitoring of continuous flow chemical synthesis using a portable, small footprint mass spectrometer.

    Bristow, Tony W T; Ray, Andrew D; O'Kearney-McMullan, Anne; Lim, Louise; McCullough, Bryan; Zammataro, Alessio

    2014-10-01

    For on-line monitoring of chemical reactions (batch or continuous flow), mass spectrometry (MS) can provide data to (1) determine the fate of starting materials and reagents, (2) confirm the presence of the desired product, (3) identify intermediates and impurities, (4) determine steady state conditions and point of completion, and (5) speed up process optimization. Recent developments in small footprint atmospheric pressure ionization portable mass spectrometers further enable this coupling, as the mass spectrometer can be easily positioned with the reaction system to be studied. A major issue for this combination is the transfer of a sample that is representative of the reaction and also compatible with the mass spectrometer. This is particularly challenging as high concentrations of reagents and products can be encountered in organic synthesis. The application of a portable mass spectrometer for on-line characterization of flow chemical synthesis has been evaluated by coupling a Microsaic 4000 MiD to the Future Chemistry Flow Start EVO chemistry system. Specifically, the Hofmann rearrangement has been studied using the on-line mass spectrometry approach. Sample transfer from the flow reactor is achieved using a mass rate attenuator (MRA) and a sampling make-up flow from a high pressure pump. This enables the appropriate sample dilution, transfer, and preparation for electrospray ionization. The capability of this approach to provide process understanding is described using an industrial pharmaceutical process that is currently under development. The effect of a number of key experimental parameters, such as the composition of the sampling make-up flow and the dilution factor on the mass spectrometry data, is also discussed. PMID:25106707

  20. Synchrotron ring as a multi-turn time-of-flight mass spectrometer

    A synchrotron ring can be used as a time-of-flight mass spectrometer under one of the two condition; a) all the particles in the ring are cooled down and have a very small momentum spread: b) the ring is tuned so as to achieve an isochronous condition for particles circulating in the ring. The methods are suited for the on-line mass measurement of short-lived nuclei which are made at an upstream production target before the injection. (author)

  1. Search for doubly-charged negative ions via accelerator mass spectrometry

    Kutschera, W.; Frekers, D.; Pardo, R.; Rehm, K.E.; Smither, R.K.; Yntema, J.L.

    1983-01-01

    The Argonne FN tandem accelerator in conjunction with an Enge split-pole magnetic spectrograph has been used as a highly sensitive mass spectrometer to search for doubly charged negative ions of /sup 11/B, /sup 12/C and /sup 16/O. No evidence for the formation of these ions in an inverted sputter source and the subsequent acceleration in the tandem has been found. The following limits for the ratio of doubly-charged to singly-charged ions were measured: X/sup - -//X/sup -/ < 1 x 10/sup -15/, /sup 11/B; < 2 x 10/sup -15/, /sup 12/C; < 2 x 10/sup -14/, /sup 16/O. A relatively abundant formation of the short lived, metastable He/sup -/ ion in the sputter source has been observed.

  2. Volcanic Gas Emissions Mapping Using a Mass Spectrometer System

    Griffin, Timothy P.; Diaz, J. Andres

    2008-01-01

    The visualization of hazardous gaseous emissions at volcanoes using in-situ mass spectrometry (MS) is a key step towards a better comprehension of the geophysical phenomena surrounding eruptive activity. In-Situ gas data consisting of helium, carbon dioxide, sulfur dioxide, and other gas species, were acquired with an MS system. MS and global position system (GPS) data were plotted on ground imagery, topography, and remote sensing data collected by a host of instruments during the second Costa Rica Airborne Research and Technology Applications (CARTA) mission This combination of gas and imaging data allowed 3-dimensional (3-D) visualization of the volcanic plume end the mapping of gas concentration at several volcanic structures and urban areas This combined set of data has demonstrated a better tool to assess hazardous conditions by visualizing and modeling of possible scenarios of volcanic activity. The MS system is used for in-situ measurement of three-dimensional gas concentrations at different volcanic locations with three different transportation platforms, aircraft, auto, and hand carried. The demonstration for urban contamination mapping is also presented as another possible use for the MS system.

  3. Fast magnetic peak switching for thermal ionization mass spectrometers

    Common practice in thermal ionization mass spectrometry is to make repeated and rapid comparisons between isotopes of interest by switching the magnetic deflection field sequentially between the values required to deflect each isotope through the collector slit. After each step in the field value (peak switch) it is necessary to pause before logging data, in order to allow the system response to settle to the point where it does not affect the precision of the isotopic ratio determination. The dynamics of the field stabilization system are the principle contributors to this delay period. The system characteristics applicable to a field-controlled magnet system are analyzed in this paer. Possible areas where the step response may be improved by the application of modern control theory are outlined. It is shown that any field-stabilized magnet system can be optimized for step response by the synthesis of a discrete control system. Discrete digital control, i.e. a software implementation, allows system optimization without the necessity for hardware modification, which would be difficult, expensive and possibility in some cases impractical. (orig.)

  4. Influence of the Ion Source Operating Conditions on the Characteristics of a Prism Mass Spectrometer With Inhomogeneous Magnetic Field

    P.O. Kuzema

    2010-01-01

    Full Text Available The influence of magnetic field focusing the electron beam in ion source of mass spectrometer on the analytical characteristics of the instrument has been studied. The range of current of ion source's focusing electromagnet providing the optimal performance of the mass spectrometer has been determined.

  5. Mass- and energy-analyses of ions from plasma by means of a miniature Thomson spectrometer

    The paper presents an improved version of a miniature mass-spectrometer of the Thomson-type, which has been adopted for ion analysis near the dense plasma region inside a vacuum chamber. Problems connected with the separation of ions from plasma streams are considered. Input diaphragms and pumping systems, needed to ensure good vacuum inside the analyzing region, are described. The application of the miniature Thomson-type analyzer is illustrated by ion parabolas recorded in plasma-focus facility and rod plasma injector experiment. A quantitative analysis of the recorded ion parabolas is presented. Factors influencing accuracy of the ion analysis are discussed and methods of the spectrometer calibration are described.

  6. Construction status of the three-stage mass spectrometer for plutonium isotope measurements

    The purpose of the three-stage high sensitivity mass spectrometer currently being assembled at the Savannah River Laboratory (SRL) is to provide ultra low-level isotope analyses to support current research programs. Initially, the instrument will measure isotope ratios required for research on plutonium transport in the environment and for determining the characteristics of plutonium-bearing particles. Also, the spectrometer will be expected to support other environmental research, in particular, research programs concerning long-lived fission products in the environment

  7. Accelerator mass spectrometry as a bioanalytical tool for nutritional research

    Vogel, J.S.; Turteltaub, K.W.

    1997-09-01

    Accelerator Mass Spectrometry is a mass spectrometric method of detecting long-lived radioisotopes without regard to their decay products or half-life. The technique is normally applied to geochronology, but recently has been developed for bioanalytical tracing. AMS detects isotope concentrations to parts per quadrillion, quantifying labeled biochemicals to attomole levels in milligram- sized samples. Its advantages over non-isotopeic and stable isotope labeling methods are reviewed and examples of analytical integrity, sensitivity, specificity, and applicability are provided.

  8. High mass resolution time of flight mass spectrometer for measuring products in heterogeneous catalysis in highly sensitive microreactors

    We demonstrate a combined microreactor and time of flight system for testing and characterization of heterogeneous catalysts with high resolution mass spectrometry and high sensitivity. Catalyst testing is performed in silicon-based microreactors which have high sensitivity and fast thermal response. Gas analysis is performed with a time of flight mass spectrometer with a modified nude Bayard-Alpert ionization gauge as gas ionization source. The mass resolution of the time of flight mass spectrometer using the ion gauge as ionization source is estimated to m/Δm > 2500. The system design is superior to conventional batch and flow reactors with accompanying product detection by quadrupole mass spectrometry or gas chromatography not only due to the high sensitivity, fast temperature response, high mass resolution, and fast acquisition time of mass spectra but it also allows wide mass range (0–5000 amu in the current configuration). As a demonstration of the system performance we present data from ammonia oxidation on a Pt thin film showing resolved spectra of OH and NH3.

  9. High mass resolution time of flight mass spectrometer for measuring products in heterogeneous catalysis in highly sensitive microreactors

    Andersen, T.; Jensen, R.; Christensen, M. K.; Pedersen, T.; Hansen, O.; Chorkendorff, I.

    2012-07-01

    We demonstrate a combined microreactor and time of flight system for testing and characterization of heterogeneous catalysts with high resolution mass spectrometry and high sensitivity. Catalyst testing is performed in silicon-based microreactors which have high sensitivity and fast thermal response. Gas analysis is performed with a time of flight mass spectrometer with a modified nude Bayard-Alpert ionization gauge as gas ionization source. The mass resolution of the time of flight mass spectrometer using the ion gauge as ionization source is estimated to m/Δm > 2500. The system design is superior to conventional batch and flow reactors with accompanying product detection by quadrupole mass spectrometry or gas chromatography not only due to the high sensitivity, fast temperature response, high mass resolution, and fast acquisition time of mass spectra but it also allows wide mass range (0-5000 amu in the current configuration). As a demonstration of the system performance we present data from ammonia oxidation on a Pt thin film showing resolved spectra of OH and NH3.

  10. High mass resolution time of flight mass spectrometer for measuring products in heterogeneous catalysis in highly sensitive microreactors

    Andersen, T.; Jensen, R.; Christensen, M. K.; Chorkendorff, I. [Department of Physics, Danish National Research Foundation' s Center for Individual Nanoparticle Functionality (CINF), Technical University of Denmark, Building 312, DK-2800 Kgs. Lyngby (Denmark); Pedersen, T.; Hansen, O. [Department of Micro- and Nanotechnology, Technical University of Denmark, DTU Nanotech Building 345 East, DK-2800 Kgs. Lyngby (Denmark)

    2012-07-15

    We demonstrate a combined microreactor and time of flight system for testing and characterization of heterogeneous catalysts with high resolution mass spectrometry and high sensitivity. Catalyst testing is performed in silicon-based microreactors which have high sensitivity and fast thermal response. Gas analysis is performed with a time of flight mass spectrometer with a modified nude Bayard-Alpert ionization gauge as gas ionization source. The mass resolution of the time of flight mass spectrometer using the ion gauge as ionization source is estimated to m/{Delta}m > 2500. The system design is superior to conventional batch and flow reactors with accompanying product detection by quadrupole mass spectrometry or gas chromatography not only due to the high sensitivity, fast temperature response, high mass resolution, and fast acquisition time of mass spectra but it also allows wide mass range (0-5000 amu in the current configuration). As a demonstration of the system performance we present data from ammonia oxidation on a Pt thin film showing resolved spectra of OH and NH{sub 3}.

  11. High mass resolution time of flight mass spectrometer for measuring products in heterogeneous catalysis in highly sensitive microreactors.

    Andersen, T; Jensen, R; Christensen, M K; Pedersen, T; Hansen, O; Chorkendorff, I

    2012-07-01

    We demonstrate a combined microreactor and time of flight system for testing and characterization of heterogeneous catalysts with high resolution mass spectrometry and high sensitivity. Catalyst testing is performed in silicon-based microreactors which have high sensitivity and fast thermal response. Gas analysis is performed with a time of flight mass spectrometer with a modified nude Bayard-Alpert ionization gauge as gas ionization source. The mass resolution of the time of flight mass spectrometer using the ion gauge as ionization source is estimated to m/Δm > 2500. The system design is superior to conventional batch and flow reactors with accompanying product detection by quadrupole mass spectrometry or gas chromatography not only due to the high sensitivity, fast temperature response, high mass resolution, and fast acquisition time of mass spectra but it also allows wide mass range (0-5000 amu in the current configuration). As a demonstration of the system performance we present data from ammonia oxidation on a Pt thin film showing resolved spectra of OH and NH(3). PMID:22852722

  12. High-performance multiple-reflection time-of-flight mass spectrometers for research with exotic nuclei and for analytical mass spectrometry

    Plaß, Wolfgang R.; Dickel, Timo; Ayet San Andres, Samuel; Ebert, Jens; Greiner, Florian; Hornung, Christine; Jesch, Christian; Lang, Johannes; Lippert, Wayne; Majoros, Tamas; Short, Devin; Geissel, Hans; Haettner, Emma; Reiter, Moritz P.; Rink, Ann-Kathrin; Scheidenberger, Christoph; Yavor, Mikhail I.

    2015-11-01

    A class of multiple-reflection time-of-flight mass spectrometers (MR-TOF-MSs) has been developed for research with exotic nuclei at present and future accelerator facilities such as GSI and FAIR (Darmstadt), and TRIUMF (Vancouver). They can perform highly accurate mass measurements of exotic nuclei, serve as high-resolution, high-capacity mass separators and be employed as diagnostics devices to monitor the production, separation and manipulation of beams of exotic nuclei. In addition, a mobile high-resolution MR-TOF-MS has been developed for in situ applications in analytical mass spectrometry ranging from environmental research to medicine. Recently, the MR-TOF-MS for GSI and FAIR has been further developed. A novel RF quadrupole-based ion beam switchyard has been developed that allows merging and splitting of ion beams as well as transport of ions into different directions. It efficiently connects a test and reference ion source and an auxiliary detector to the system. Due to an increase in the kinetic energy of the ions in the time-of-flight analyzer of the MR-TOF-MS, a given mass resolving power is now achieved in less than half the time-of-flight. Conversely, depending on the time-of-flight, the mass resolving power has been increased by a factor of more than two.

  13. Optimization of an indigenous thermal ionization mass spectrometer for field application in a fuel reprocessing plant

    Reprocessing of spent fuels is an important step in the entire nuclear fuel cycle for a sustained nuclear energy programme in our country. Thermal ionization mass spectrometry (TIMS) has been recognized as the most reliable and suitable method for Input Accountability of plutonium and uranium in reprocessing plant. To meet this requirement, a thermal ionization mass spectrometer (TIMS-3) has been developed indigenously by TPPED, BARC, Mumbai, India and is installed at Accountability laboratory of KARP, Kalpakkam. Instrument has been designed based on user specifications which is in line with current generation commercial thermal ionization mass spectrometer. The objective of this present work is to evaluate performance characteristics of the instrument and optimize its capabilities to make it suitable for regular application in the reprocessing plant. Some of the performances of this instrument and the quality of analytical out-put has been already discussed. Present paper discusses the further works carried out in standardizing the instrument with various calibrations and arbitration

  14. Mobile high-resolution time-of-flight mass spectrometer for in-situ analytics

    Lang, Johannes; Ebert, Jens [II. Physikalisches Institut, JLU, Giessen (Germany); Dickel, Timo; Geissel, Hans; Plass, Wolfgang; Scheidenberger, Christoph [II. Physikalisches Institut, JLU, Giessen (Germany); GSI, Darmstadt (Germany)

    2011-07-01

    A compact multiple-reflection time-of-flight mass spectrometer (MR-TOF-MS) has been developed. For the first time it allows for mass measurements with a resolving power exceeding 100000 and sub ppm accuracy in a mobile device. Thus it allows to resolve isobars and enables to accurately determine the composition and structure of biomolecules. The MR-TOF-MS consists of an atmospheric pressure interface for DESI and REIMS, ion cooler, ion trap, time-of-flight analyzer, MCP detector and DAQ. Vacuum system components, power supplies as well as electronics are mounted together with the ion optical spectrometer parts on a single frame with a total volume of 0.8 m{sup 3}. Applications of the device within the AmbiProbe research program include in-situ mass spectrometry such as real-time tissue recognition in electrosurgery, identification of mycotoxins and analysis of soil samples for environmental studies.

  15. Mobile high-resolution time-of-flight mass spectrometer for in-situ analytics

    A compact multiple-reflection time-of-flight mass spectrometer (MR-TOF-MS) has been developed. For the first time it allows for mass measurements with a resolving power exceeding 100000 and sub ppm accuracy in a mobile device. Thus it allows to resolve isobars and enables to accurately determine the composition and structure of biomolecules. The MR-TOF-MS consists of an atmospheric pressure interface for DESI and REIMS, ion cooler, ion trap, time-of-flight analyzer, MCP detector and DAQ. Vacuum system components, power supplies as well as electronics are mounted together with the ion optical spectrometer parts on a single frame with a total volume of 0.8 m3. Applications of the device within the AmbiProbe research program include in-situ mass spectrometry such as real-time tissue recognition in electrosurgery, identification of mycotoxins and analysis of soil samples for environmental studies.

  16. Laser Ion Acceleration from Mass-Limited Targets with Preplasma

    Lezhnin, K V; Esirkepov, T Zh; Bulanov, S V; Klimo, O; Weber, S; Korn, G

    2016-01-01

    The interaction of high intensity laser radiation with mass-limited target exhibits significant enhancement of the ion acceleration when the target is surrounded by an underdense plasma corona, as seen in numerical simulations. The self-generated quasistatic magnetic field squeezes the corona causing the intensification of a subsequent Coulomb explosion of the target. The electric field intensification at the target edges and plasma resonance effects result in the generation of characteristic density holes and further contributes to the ion acceleration.The interaction of high intensity laser radiation with mass-limited target exhibits significant enhancement of the ion acceleration when the target is surrounded by an underdense plasma corona, as seen in numerical simulations. The self-generated quasistatic magnetic field squeezes the corona causing the intensification of a subsequent Coulomb explosion of the target. The electric field intensification at the target edges and plasma resonance effects result in...

  17. A Bragg curve ionization chamber for acceleration mass spectrometry

    An ionization chamber based on the Bragg curve spectrometry method to be used as the final detector in a accelerator mass spectrometry system is described. The first tests with a Cl beam give energy resolution of 1% and Z resolving power of 72 at Z=17

  18. Neutrino mass and mixing, and non-accelerator experiments

    We review the current status of experimental knowledge about neutrinos derived from kinematic mass measurements, neutrino oscillation searches at reactors and accelerators, solar neutrinos, atmospheric neutrinos, and single and double beta decay. The solar neutrino results yield fairly strong and consistent indication that neutrino oscillations are occurring. Other evidence for new physics is less consistent and convincing

  19. A Method for Estimating Mass-Transfer Coefficients in a Biofilter from Membrane Inlet Mass Spectrometer Data

    Nielsen, Anders Michael; Nielsen, Lars Peter; Feilberg, Anders;

    2009-01-01

    A membrane inlet mass spectrometer (MIMS) was used in combination with a developed computer model to study and improve management of a biofilter (BF) treating malodorous ventilation air from a meat rendering facility. The MIMS was used to determine percentage removal efficiencies (REs) of selected...... sulfur gases and to provide toluene retention profiles for the model to determine the air velocity and overall mass-transfer coefficient of toluene. The mass-transfer coefficient of toluene was used as a reference for determining the mass transfer of sulfur gases. By presenting the model to scenarios of......, knowing the relationship between mass-transfer coefficients and air velocity for a given type of BF allows for an improved dimensioning and managing of this and similar BFs. This research demonstrates that it is possible to estimate mass-transfer coefficients and air velocity in BFs using MIMS in...

  20. Accelerator mass spectrometry at the University of North Texas

    Anthony, J. M.; Matteson, S.; McDaniel, F. D.; Duggan, J. L.

    1989-04-01

    An accelerator mass spectrometry system designed for analysis of electronic materials is being developed and installed on the University of North Texas 3 MV tandem accelerator (National Electrostatics Corporation 9-SDH). High-resolution magnetic (40° deflection, {M}/{ΔM ≈ 350}, maximum mass-energy product 69 MeVu) and electro static (45 ° deflection, E/ q of 4.8 MeV, {E}/{ΔE}≈ 730 ) analysis, coupled with a 1.5 m time-of-flight path and total energy detection (surface barrier detector) forms the basis of the detection system. In order to provide stable element detection capability at the parts-per-trillion level in electronic materials (Si, GaAs, HgCdTe), a custom ion source, incorporating mass analysis of the sputtering beam, ultraclean slits, low cross-contamination and UHV capability, is being constructed.

  1. Solid state magnet control unit for an A.E.I. MS-902 mass spectrometer

    The computerized gas chromatograph-mass spectrometer (GC-MS) technique is used extensively for the study of metabolic disorders. The MS-902 mass spectrometer used by the authors is equipped with a 2-s scanning facility which is used for GC-MS applications. When the spectrometer is operated in a continuous magnetic scanning mode at this scan rate, the magnetic field frequently drifts in the course of a GC analysis. Therefore, it has been impossible to determine automatically the mass peak centroids (usually measured in time from a preset magnetic field) and obtain correct mass to charge (m/z) values for the ions. The instability of the magnetic field arises from the heat generated in the vacuum tube magnet regulator under dynamic scanning conditions. To overcome this problem the vacuum tubes in the regulator must be changed every two to three months. The high cost of some of these tubes, particularly of the three 13 EI control tubes, led to the design and construction of a solid state magnet control unit which is described in this communication. (Auth.)

  2. Direct trace analysis of metals and alloys in a quadrupole ion-trap mass spectrometer

    Song, K S; Yang, M; Cha, H K; Lee, J M; Lee, G H

    1999-01-01

    An ion-trap mass spectrometer adopting a quadrupole ion-trap and laser ablation/ionization method was constructed. The developed system was tested for composition analysis of some metals (Cu, stainless), and alloys (hastalloy C, mumetal) by mass spectrometry. Samples were analyzed by using laser ablation from a sample probe tip followed by a mass analysis with the quadrupole ion-trap. The quadrupole ion-trap was modified to enable laser ablation by a XeCl excimer laser pulse that passed radially through the ring electrode. A mass scan of the produced ions was performed in the mass selective instability mode wherein trapped ions were successively detected by increasing the rf voltage through the ring electrode. Factors affecting the mass resolution, such as pressure of buffer gas and ablation laser power, are discussed.

  3. Accelerating field spectrometer for photons and electrons simultaneous measurement. Application to decay schemes study

    An original spectrometer was built to improve the measurement of the absolute emission intensities of radionuclides with converted low energy gamma transitions. In this spectrometer, the same Si(Li) detector simultaneously measures electrons and photons emitted by the studied radionuclide; an electrostatic field may be established between the source and the detector to modify the electrons energy. This field allows the electron and photon peaks to be separated, and the absorption and energy straggling by detector windows to be decreased. Special attention has been given to determine spectrometer efficiency calibration curves for electrons and photons. 147Nd and 133Ba were used to test the spectrometer improvement and the method used

  4. Recursive least square vehicle mass estimation based on acceleration partition

    Feng, Yuan; Xiong, Lu; Yu, Zhuoping; Qu, Tong

    2014-05-01

    Vehicle mass is an important parameter in vehicle dynamics control systems. Although many algorithms have been developed for the estimation of mass, none of them have yet taken into account the different types of resistance that occur under different conditions. This paper proposes a vehicle mass estimator. The estimator incorporates road gradient information in the longitudinal accelerometer signal, and it removes the road grade from the longitudinal dynamics of the vehicle. Then, two different recursive least square method (RLSM) schemes are proposed to estimate the driving resistance and the mass independently based on the acceleration partition under different conditions. A 6 DOF dynamic model of four In-wheel Motor Vehicle is built to assist in the design of the algorithm and in the setting of the parameters. The acceleration limits are determined to not only reduce the estimated error but also ensure enough data for the resistance estimation and mass estimation in some critical situations. The modification of the algorithm is also discussed to improve the result of the mass estimation. Experiment data on a sphalt road, plastic runway, and gravel road and on sloping roads are used to validate the estimation algorithm. The adaptability of the algorithm is improved by using data collected under several critical operating conditions. The experimental results show the error of the estimation process to be within 2.6%, which indicates that the algorithm can estimate mass with great accuracy regardless of the road surface and gradient changes and that it may be valuable in engineering applications. This paper proposes a recursive least square vehicle mass estimation method based on acceleration partition.

  5. A Compact Ion and Neutral Mass Spectrometer for the Exocube Mission

    Jones, S.; Paschalidis, N.; Rodriguez, M.; Sittler, E. C., Jr.; Chornay, D. J.

    2014-12-01

    Demand is high for in situ measurements of atmospheric neutral and ion composition and density, not only for studies of the dynamic ionosphere-theremosphere-mesosphere system but simply to define the steady state background atmospheric conditions. The ExoCube mission is designed to acquire global knowledge of in-situ densities of [H], [He], [O] and [H+], [He+], [O+] in the upper ionosphere and lower exosphere in combination with incoherent scatter radar ground stations distributed in the north polar region. The Heliophysic Division of GSFC has developed a compact Ion and Neutral Mass Spectrometer (INMS) for in situ measurements of ions and neutrals H, He, N, O, N2, O2 with M/dM of approximately 10 at an incoming energy range of 0-50eV. The INMS is based on front end optics, post acceleration, gated time of flight, ESA and CEM or MCP detectors. The compact sensor has a dual symmetric configuration with the ion and neutral sensor heads on opposite sides and with full electronics in the middle. The neutral front end optics includes thermionic emission ionization and ion blocking grids, and the ion front end optics includes spacecraft potential compensation grids. The electronics include front end, fast gating, HVPS, ionizer, TOF binning and full bi directional C&DH digital electronics. The data package includes 400 mass bins each for ions and neutrals and key housekeeping data for instrument health and calibration. The data sampling can be commanded as fast as 10 msec per frame (corresponding to ~80 m spatial separation) in burst mode, and has significant onboard storage capability and data compression scheme. Experimental data from instrument testing with both ions and neutrals will be presented. The instrument is successfully integrated in the CubeSat and passed vibration, thermal and shock testing. The ExoCube mission is scheduled to fly in Nov 2014 in a 445 x 670 km polar orbit with the INMS aperture oriented in the ram direction. This miniaturized instrument (1

  6. Toward laser ablation Accelerator Mass Spectrometry of actinides

    A project to measure neutron capture cross sections of a number of actinides in a reactor environment by Accelerator Mass Spectrometry (AMS) at the ATLAS facility of Argonne National Laboratory is underway. This project will require the precise and accurate measurement of produced actinide isotopes in many (>30) samples irradiated in the Advanced Test Reactor at Idaho National Laboratory with neutron fluxes having different energy distributions. The AMS technique at ATLAS is based on production of highly-charged positive ions in an electron cyclotron resonance (ECR) ion source followed by acceleration in the ATLAS linac and mass-to-charge (m/q) measurement at the focus of the Fragment Mass Analyzer. Laser ablation was selected as the method of feeding the actinide material into the ion source because we expect it will have higher efficiency and lower chamber contamination than either the oven or sputtering techniques, because of a much narrower angular distribution of emitted material. In addition, a new multi-sample holder/changer to allow quick change between samples and a computer-controlled routine allowing fast tuning of the accelerator for different beams, are being developed. An initial test run studying backgrounds, detector response, and accelerator scaling repeatability was conducted in December 2010. The project design, schedule, and results of the initial test run to study backgrounds are discussed.

  7. Toward laser ablation Accelerator Mass Spectrometry of actinides

    Pardo, R. C.; Kondev, F. G.; Kondrashev, S.; Nair, C.; Palchan, T.; Scott, R.; Seweryniak, D.; Vondrasek, R.; Paul, M.; Collon, P.; Deibel, C.; Youinou, G.; Salvatores, M.; Palmotti, G.; Berg, J.; Fonnesbeck, J.; Imel, G.

    2013-01-01

    A project to measure neutron capture cross sections of a number of actinides in a reactor environment by Accelerator Mass Spectrometry (AMS) at the ATLAS facility of Argonne National Laboratory is underway. This project will require the precise and accurate measurement of produced actinide isotopes in many (>30) samples irradiated in the Advanced Test Reactor at Idaho National Laboratory with neutron fluxes having different energy distributions. The AMS technique at ATLAS is based on production of highly-charged positive ions in an electron cyclotron resonance (ECR) ion source followed by acceleration in the ATLAS linac and mass-to-charge (m/q) measurement at the focus of the Fragment Mass Analyzer. Laser ablation was selected as the method of feeding the actinide material into the ion source because we expect it will have higher efficiency and lower chamber contamination than either the oven or sputtering techniques, because of a much narrower angular distribution of emitted material. In addition, a new multi-sample holder/changer to allow quick change between samples and a computer-controlled routine allowing fast tuning of the accelerator for different beams, are being developed. An initial test run studying backgrounds, detector response, and accelerator scaling repeatability was conducted in December 2010. The project design, schedule, and results of the initial test run to study backgrounds are discussed.

  8. Toward a Micro Gas Chromatograph/Mass Spectrometer (GC/MS) System

    Wiberg, D. V.; Eyre, F. B.; Orient, O.; Chutjian, A.; Garkarian, V.

    2001-01-01

    Miniature mass filters (e.g., quadrupoles, ion traps) have been the subject of several miniaturization efforts. A project is currently in progress at JPL to develop a miniaturized Gas Chromatograph/Mass Spectrometer (GC/MS) system, incorporating and/or developing miniature system components including turbomolecular pumps, scroll type roughing pump, quadrupole mass filter, gas chromatograph, precision power supply and other electronic components. The preponderance of the system elements will be fabricated using microelectromechanical systems (MEMS) techniques. The quadrupole mass filter will be fabricated using an X-ray lithography technique producing high precision, 5x5 arrays of quadrupoles with pole lengths of about 3 mm and a total volume of 27 cubic mm. The miniature scroll pump will also be fabricated using X-ray lithography producing arrays of scroll stages about 3 mm in diameter. The target detection range for the mass spectrometer is 1 to 300 atomic mass units (AMU) with are solution of 0.5 AMU. This resolution will allow isotopic characterization for geochronology, atmospheric studies and other science efforts dependant on the understanding of isotope ratios of chemical species. This paper will discuss the design approach, the current state-of-the art regarding the system components and the progress toward development of key elements. The full system is anticipated to be small enough in mass, volume and power consumption to allow in situ chemical analysis on highly miniaturized science craft for geochronology, atmospheric characterization and detection of life experiments applicable to outer planet roadmap missions.

  9. The suprathermal ion mass spectrometer (SMS) onboard the Akebono (EXOS-D) satellite

    The suprathermal ion mass spectrometer (SMS) was developed to study the thermal and suprathermal ion distributions in the low altitude magnetosphere. The instrument has a mass and plasma density dynamic range sufficient to measure, on a regular basis, the major and the minor ion distribution functions at apogee as well as at perigee. The instrument is a radio frequency type mass spectrometer and has a programmable mass resolution which is independent of energy and mass selected. The present report gives measurements of the thermal ion mass composition near apogee which show that the composition varies from one dominated by H+ and O+ to one in which the density of 'minor' ions (O++, He+, N+) is comparable to or greater than that of H+ and O+. The report also prevents high time resolution mass/energy/angle observations in the topside ionospheric plasma in or near the cusp region where rapid heating of the bulk of the plasma and the formation of conic distributions is evident. These unique observations are compared with other plasma diagnostrics on the spacecraft to improve the understanding of ionospheric ion production, convection and loss processes as well as low altitude ion energization phenomena. (N.K.)

  10. The Multiplexed Chemical Kinetic Photoionization Mass Spectrometer: A New Approach To Isomer-resolved Chemical Kinetics

    Osborne, David L.; Zou, Peng; Johnsen, Howard; Hayden, Carl C.; Taatjes, Craig A.; Knyazev, Vadim D.; North, Simon W.; Peterka, Darcy S.; Ahmed, Musahid; Leone, Stephen R.

    2008-08-28

    We have developed a multiplexed time- and photon-energy?resolved photoionizationmass spectrometer for the study of the kinetics and isomeric product branching of gasphase, neutral chemical reactions. The instrument utilizes a side-sampled flow tubereactor, continuously tunable synchrotron radiation for photoionization, a multi-massdouble-focusing mass spectrometer with 100percent duty cycle, and a time- and positionsensitive detector for single ion counting. This approach enables multiplexed, universal detection of molecules with high sensitivity and selectivity. In addition to measurement of rate coefficients as a function of temperature and pressure, different structural isomers can be distinguished based on their photoionization efficiency curves, providing a more detailed probe of reaction mechanisms. The multiplexed 3-dimensional data structure (intensity as a function of molecular mass, reaction time, and photoionization energy) provides insights that might not be available in serial acquisition, as well as additional constraints on data interpretation.

  11. The ion optics of a miniature 3He/4He mass spectrometer of high resolution

    To measure the isotopic abundance ratio of 3He and 4He in samples by mass spectrometers is an important detection mean for helium isotope geochemistry research. A symmetrically arranged tandem 3He/4He mass spectrometer is described in the paper. The front stage, used to analyse 3He (including HD and H3) and 4He, is a homogeneous analysing magnet with a bending angle of 90 deg and a bending radius of 6 cm. The end stage, used to analyse 3He, HD and H3, is a non-homogeneous analysing magnet with a bending angle of 180 deg, a bending radius of 15 cm and a magnetic field gradient of 0.75. Because of the use of the non-zero second order coefficient β and curved entrance face of the later magnet for eliminating second order aberrations, the resolving power of the system is notably improved, and theoretically reaches about 3800

  12. Development and Evaluation of a Variable-Temperature Quadrupole Ion Trap Mass Spectrometer

    Derkits, David; Wiseman, Alex; Snead, Russell F.; Dows, Martina; Harge, Jasmine; Lamp, Jared A.; Gronert, Scott

    2016-02-01

    A new, variable-temperature mass spectrometer system is described. By applying polyimide heating tape to the end-cap electrodes of a Bruker (Bremen, Germany) Esquire ion trap, it is possible to vary the effective temperature of the system between 40 and 100°C. The modification does not impact the operation of the ion trap and the heater can be used for extended periods without degradation of the system. The accuracy of the ion trap temperatures was assessed by examining two gas-phase equilibrium processes with known thermochemistry. In each case, the variable-temperature ion trap provided data that were in good accord with literature data, indicating the effective temperature in the ion trap environment was being successfully modulated by the changes in the set-point temperatures on the end-cap electrodes. The new design offers a convenient and effective way to convert commercial ion trap mass spectrometers into variable-temperature instruments.

  13. Direct mass measurements of light neutron-rich nuclei using fast recoil spectrometers

    Extensive new mass measurement capabilities have evolved with the development of recoil spectrometers. In the Z = 3 to 9 neutron-rich region alone, 12 neutron-rich nuclei have been determined for the first time by the fast-recoil direct mass measurement method. A recent experiment using the TOFI spectrometer illustrates this technique. A systematic investigation of nuclei that lie along or near the neutron-drip line has provided a valuable first glimpse into the nuclear structure of such nuclei. No evidence for a large single-particle energy gap at N = 14 is observed; however, a change in the two-neutron separation model calculations, and is interpreted in terms of the smaller 1s/sub 1/2/ - 1s/sub 1/2/ interaction compared to that of the 0d/sub 5/2/ - 0d/sub 5/2/ neutron-neutron interaction. 18 refs., 7 figs., 1 tab

  14. Fabrication and testing of the recoil mass spectrometer at Bombay Pelletron

    S Nagaraj; H C Jain; P K Joshi; S D Paul; R Palit; H V Panchal; B S Naidu; A Chatterjee; A Navin

    2001-07-01

    A recoil mass spectrometer (RMS) has been designed, fabricated and installed at the 15°S beam-line of the Pelletron at TIFR. The RMS consists of a quadrupole doublet just after the target chamber followed by an ‘electrostatic deflector’, a magnetic dipole and a second electrostatic deflector. The recoils produced in the 12C+58Ni reaction using 60 MeV 12C beam were focussed with the help of electric and magnetic fields and detected in a strip detector placed at the focal plane of the RMS. Further testing of the spectrometer to obtain mass resolution and efficiency are in progress.

  15. Field test of a thermal quadrupole mass spectrometer for safeguards verification

    A thermal ionization quadrupole mass spectrometer (Finnigan MAT) was tested in the Safeguards Analytical Laboratory of the IAEA with a view to evaluating its potential field applications. Several modifications have been introduced by the manufacturer. The instrument is equipped with an electron multiplier system and a Faraday cup detector. It allows fully automated analysis. Loadings of 1 μg U and 50 ng Pu can be measured without any problem. (author)

  16. Performance Characteristics of a New Hybrid Triple Quadrupole Time-of-Flight Tandem Mass Spectrometer

    Andrews, Genna L.; Simons, Brigitte L.; Young, J. Bryce; Hawkridge, Adam M.; David C Muddiman

    2011-01-01

    The TripleTOF 5600 System, a hybrid triple quadrupole time-of-flight mass spectrometer, was evaluated to explore the key figures of merit in generating peptide and protein identifications which included spectral acquisition rates, data quality, proteome coverage, and biological depth. Employing a Saccharomyces cerevisiae tryptic digest, careful consideration of several performance features demonstrated that the speed of the TripleTOF contributed most to the resultant data. The TripleTOF syste...

  17. CologneAMS, a dedicated center for accelerator mass spectrometry in Germany

    Dewald, A., E-mail: dewald@ikp.uni-koeln.de [CologneAMS, Institute of Nuclear Physics, University of Cologne (Germany); Heinze, S.; Jolie, J.; Zilges, A. [CologneAMS, Institute of Nuclear Physics, University of Cologne (Germany); Dunai, T.; Rethemeyer, J.; Melles, M.; Staubwasser, M. [Institute of Geology and Mineralogy, University of Cologne (Germany); Kuczewski, B. [Division of Nuclear Chemistry, University of Cologne (Germany); Richter, J. [Institute of Prehistoric Archaeology, University of Cologne (Germany); Radtke, U. [Institute of Geography, University of Cologne, Germany, Rectorate, University of Duisburg-Essen (Germany); Blanckenburg, F. von [GFZ, German Research Centre for Geosciences, Potsdam (Germany); Klein, M. [HVEE, Amersfoort (Netherlands)

    2013-01-15

    CologneAMS is a new centre for accelerator mass spectrometry (AMS) at University of Cologne. It has been funded by the German Research Foundation (DFG) to improve the experimental conditions especially for those German scientists that apply the AMS technique for their geologic, environmental, nuclear chemical, and nuclear astrophysical research. The new AMS-device has been built by High Voltage Engineering Europe (HVEE) and has been installed in the existing accelerator area of the Institute of Nuclear Physics. The AMS-facility is designed for the spectrometry of {sup 10}Be, {sup 14}C, {sup 26}Al, {sup 36}Cl, {sup 41}Ca, {sup 129}I in and heavy ions up to {sup 236}U and {sup 244}Pu. The central part of the AMS-facility is a 6 MV Tandetron Trade-Mark-Sign accelerator. Downstream of the high energy mass spectrometer an additional switching magnet is used as a further filter element which supplies also additional ports for future extensions of the detector systems. The current status of CologneAMS and the results of the first test measurements will be presented.

  18. Analytical applications of ion/molecule reactions in a triple quadrupole mass spectrometer

    The development of triple quadrupole mass spectrometers as a means of performing tandem mass spectrometry has provided a versatile instrument on which the ion/molecule reactions of a mass selected ion can be studied. This dissertation details the application of ion/molecule reactions in a triple quadrupole to two analytical problems. Part I. Ion/Molecule Reactions of Ammonia with Translationally Excited C2H5O+/Ions. The ability to impart low center-of-mass translational energies, which upon collision are converted into internal energy, allows the observation of reactions that require energy input. In addition, the systematic variation of the ion kinetic energy, often referred to as energy-resolved mass spectrometer, adds another dimension to the mass spectrum and can allow the observation of thresholds for reactions requiring energy input. This investigation develops methods for determining these thresholds. Part 2. The Use of Ion/Molecule Reactions in selected Reaction Monitoring GC/MSD/MS Analyses. An approach to improving the selectivity of an analysis is to improve the selectivity of the detection method. In GC/MS, one method has been to monitor a selected fragmentation reaction, either metastable or collisionally activated, in a selected reaction monitoring (SRM) analysis. This develops the use of ion/molecule reactions for selected reaction monitoring analyses

  19. Ion-optical studies for improved ion transmission in multistage isotope-ratio mass spectrometers

    Theoretical and experimental ion-optical studies of multistage isotope-ratio mass spectrometers were conducted to determine what improvement in ion transmission efficiency might be attainable through design changes. The computer program GIOS (General Ion Optical Systems) was used to perform theoretical calculations of focusing properties and ion transmission efficiency. Actual transmission through multiple-sector instruments was determined from measurements of the ion beam vertical profile at the focus of each stage. For existing mass spectrometers with tandem magnets of normal geometry, our studies determined a feasible design change that significantly increases ion transmission through the analyzer. The use of a cylindrical einzel lens or an electrostatic quadrupole lens near the focal point between the magnets provides vertical focusing of the ion beam to achieve the improved transmission. We also established a new mass spectrometer design that give 100% transmission through tandem magnetic analyzers and through a third-stage electrostatic analyzer without the use of an intermediate focusing lens. Non-normal magnetic field boundaries provide ion beam focusing in the vertical plant to achieve this complete transmission. 19 refs., 27 figs., 3 tabs

  20. Engineering Sensitivity Improvement of Helium Mass Spectrometer Leak Detection System by Means Global Hard Vacuum Test

    The engineering sensitivity improvement of Helium mass spectrometer leak detection using global hard vacuum test configuration has been done. The purpose of this work is to enhance the sensitivity of the current leak detection of pressurized method (sniffer method) with the sensitivity of 10-3 ∼ 10-5 std cm3/s, to the global hard vacuum test configuration method which can be achieved of up to 10-8 std cm3/s. The goal of this research and development is to obtain a Helium leak test configuration which is suitable and can be used as routine bases in the quality control tests of FPM capsule and AgInCd safety control rod products. The result is an additional instrumented vacuum tube connected with conventional Helium mass spectrometer. The pressure and temperature of the test object during the leak measurement are simulated by means of a 4.1 kW capacity heater and Helium injection to test object, respectively. The addition of auxiliary mechanical vacuum pump of 2.4 l/s pumping speed which is directly connected to the vacuum tube, will reduce 86 % of evacuation time. The reduction of the measured sensitivity due to the auxiliary mechanical vacuum pump can be overcome by shutting off the pump soon after Helium mass spectrometer reaches its operating pressure condition. (author)

  1. A compact permanent magnet cyclotrino for accelerator mass spectrometry

    Young, A.T.; Clark, D.J.; Kunkel, W.B.; Leung, K.N.; Li, C.Y. [Lawrence Berkeley Lab., CA (United States)

    1995-02-01

    The authors describe the development of a new instrument for the detection of trace amounts of rare isotopes, a Cyclotron Mass Spectrometer (CMS). A compact low energy cyclotron optimized for high mass resolution has been designed and has been fabricated. The instrument has high sensitivity and is designed to measure carbon-14 at abundances of < 10{sup {minus}12}. A novel feature of the instrument is the use of permanent magnets to energize the iron poles of the cyclotron. The instrument uses axial injection, employing a spiral inflector. The instrument has been assembled and preliminary measurements of the magnetic field show that it has a uniformity on the order of 2 parts in 10{sup 4}.

  2. Optimized Fast and Sensitive Acquisition Methods for Shotgun Proteomics on a Quadrupole Orbitrap Mass Spectrometer

    Kelstrup, Christian D; Young, Clifford; Lavallee, Richard;

    2012-01-01

    (HCD) tandem mass spectra due to the parallel mode of operation, where the generation, filling, and storage of fragment ions can be performed while simultaneously measuring another ion packet in the Orbitrap mass analyzer. In this study, data-dependent acquisition methods for "fast" or "sensitive......Advances in proteomics are continually driven by the introduction of new mass spectrometric instrumentation with improved performances. The recently introduced quadrupole Orbitrap (Q Exactive) tandem mass spectrometer allows fast acquisition of high-resolution higher-energy collisional dissociation...... h of analysis time. At sample loads below 125 ng, a 156 ms HCD acquisition method improved the sensitivity, mass accuracy, and quality of data and enabled us to identify 30% more proteins and peptides than the faster scanning method. A similar effect was observed when the LC gradient was extended to...

  3. Continuous-flow accelerator mass spectrometry for radiocarbon analysis

    Accelerator Mass Spectrometry (AMS) is a widely used technique for radiocarbon dating of archaeological or environmental samples that are very small or very old (up to 50,000 years before present). Because of the method's extreme sensitivity, AMS can also serve as an environmental tracer and supplements conventional nuclear counting techniques for monitoring 14C emissions from operating nuclear power plants and waste repositories. The utility of present AMS systems is limited by the complex sample preparation process required. Carbon from combusted artefacts must be incorporated into a solid metallic target from which a negative ion beam is produced and accelerated to MeV energies by an accelerator for subsequent analysis. This paper will describe a novel technique being developed by the National Ocean Sciences Accelerator Mass Spectrometry (NOSAMS) Laboratory at the Woods Hole Oceanographic Institution for the production of negative carbon ion beams directly from a continuously flowing sample gas stream, eliminating the requirement for a solid target. A key component of the new technique is a microwave-driven, gaseous-feed ion source originally developed at Chalk River Laboratories for the very different requirements of a high current proton linear accelerator. A version of this ion source is now being adapted to serve as an injector for a dedicated AMS accelerator facility at NOSAMS. The paper begins with a review of the fundamentals of radiocarbon dating. Experiments carried out at NOSAMS with a prototype of the microwave ion source are described, including measurements of sample utilization efficiency and sample 'memory' effect. A new version of the microwave ion source, optimized for AMS, is also described. The report concludes with some predictions of new research opportunities that will become accessible to the technique of continuous-flow AMS. (author)

  4. Development of electrospray ionization of biomolecules on a magnetic sector mass spectrometer

    The initial part of this study involves developments made on an electrospray ionization (ESI) source installed on a large-scale double-focusing reverse-geometry two-sector mass spectrometer. The practical considerations and some basic theory have been given in this thesis for each of the improvements made to the ESI source. The process of partial re-designing the ion optical system showed that the ion beam was affected by both gas dynamics and by the field penetration from the lenses of the ion optical system in the region immediately after second skimmer. More than one order magnitude stronger ion signal intensities at the mass spectrometer final detector and easier ESI source operation conditions and stable ion signals has been achieved. Mass-analyzed ion kinetic energy spectroscopy (MIKES) of different charge-states of relatively small peptides (substance P and bradykinin) for collision-induced dissociation (CID) and the metastable dissociation was carried out successfully. The translational energy losses caused shifts in the fragment ion peaks in the CID spectra, compared with fragment ion peaks in the metastable dissociation spectra. A major part of the study concerned effects of ESI source condition on the charge state distributions of mass spectra. It has been shown that the ion optical effect of the potential difference (VHCT-S) between the heated stainless steel capillary (HCT) and the first skimmer in the intermediate-pressure region (capillary-skimmer region or orifice-skimmer region) of the ESI source was the main factor in determining the charge state distribution of the ESI mass spectra. The temperature of the HCT and the potential difference between the first skimmer and the second skimmer has been shown to be also important factors. The collision-induced dissociation (or so-called capillary-skimmer dissociation) effect of VHCT-S has been shown to be relatively low in this sector-mass spectrometer ESI source. (author)

  5. Development of a dedicated isotope mass spectrometer for the noninvasive diagnostics of humans infected with Helicobacter Pylori

    Blashenkov, N. M.; Sheshenya, E. S.; Solov'ev, S. M.; Gall', L. N.; Sachenko, V. M.; Zarutskii, I. V.; Gall', N. R.

    2013-06-01

    A dedicated isotope mass spectrometer for the noninvasive diagnostics of humans infected with Helicobacter Pylori using the isotope respiratory test is developed. A low-aberration mass analyzer is calculated, an input system that makes it possible to eliminate the memory effects is developed, and a small-size ion detector is constructed. The mass spectrometer is created, and the tests are performed. The measurement accuracy of the 13C/12C and 16O/18O isotope ratios are 1.7 and 2.2‰, respectively. Preliminary medical tests show that the spectrometer can be employed for the desired diagnostics.

  6. Global model of longitude/UT variations in thermospheric composition and temperature based on mass spectrometer data

    Hedin, A. E.; Reber, C. A.; Spencer, N. W.; Brinton, H. C.; Kayser, D. C.

    1979-01-01

    Measurements of N2, O, He, and Ar densities from neutral gas mass spectrometers on four satellites and inferred O2 and H densities from an ion mass spectrometer have been combined to produce a model of longitude/UT variations in thermospheric neutral composition and temperature. The longitude/UT model is an extension of the mass spectrometer-incoherent scatter thermospheric model (Hedin et al., 1977) and uses spherical harmonic terms dependent on geographic latitude, longitude, and UT. The combined longitude and UT variations reflect the influence of the geomagnetic field but indicate that the variations may not simply be represented in magnetic coordinates.

  7. A statistical investigation of the mass discrepancy-acceleration relation

    Desmond, Harry

    2016-01-01

    We use the mass discrepancy-acceleration relation (the correlation between the ratio of dark-to-visible mass and acceleration in galaxies; MDAR) to test the galaxy-halo connection. We analyse the MDAR using a set of 14 statistics which quantify its four most important features: its shape, its scatter, the presence of a "characteristic acceleration scale," and the correlation of its residuals with other galaxy properties. We construct an empirical framework for the galaxy-halo connection in $\\Lambda$CDM to generate predictions for these statistics, starting with conventional correlations (halo abundance matching; AM) and introducing more where required. Comparing to the SPARC data (Lelli, McGaugh & Schombert 2016), we find: 1) The approximate shape of the MDAR is readily reproduced by AM, and there is no evidence that the acceleration at which dark matter becomes negligible has less spread in the data than in AM mocks; 2) Even under conservative assumptions, AM significantly overpredicts the scatter in the...

  8. Design and realization of a space-borne reflectron time of flight mass spectrometer: electronics and measuring head

    The purpose of this thesis is the design of the electronics of a time of flight mass spectrometer, the making and the vacuum tests of a prototype which can be put onboard a satellite. A particular effort was necessary to decrease to the maximum the mass and electric consumption of the spectrometer, which led to the development of new circuits. The work completed during this thesis initially concerns the electronics of the measuring equipment which was conceived in a concern for modularity. A complete 'reflectron' type mass spectrometer was then designed, simulated and developed. The built prototype, which uses the developed electronics, was exposed to ion flows of different masses and energies in the CESR vacuum chambers. Its measured performances validate the implemented principles and show that an identical mass spectrometer can be put onboard a satellite with profit, for planetary or solar missions. (author)

  9. Preliminary description of a dedicated commercial ultra-sensitive mass spectrometer for direct atom counting of 14C

    A description is presented of a commercial, tandem-accelerator centered secondary ion double mass spectrometer dedicated to 14C/13C/12C ratio measurements. Some design philosophy of the instrument is presented and the performance is described. A scanning cesium ion source with primary beam diameters between 100 to 200 micrometers is used to produce C- beam intensities of 10 to 20μA with the intensities remaining constant to better than 0.1% per minute after the source stabilizes. For recent carbon, these currents correspond to 14C count rates from the ion source of 60 to 120 particles per second. Resolution of the first mass defining system, M/ΔM, is greater than 120 with the capability of rapid mass switching between isotopes. The measured isotopic ratios at the ion source for carbon are constant to better than 0.25%. The virtues of the 3MV parallel-fed Cockroft-Walton accelerator supply are presented. At the operating voltage of 2.5MV, the stability is better than 1:4000 with a terminal ripple 13C3+ and 12C3+ ions which originate from mass-14 molecular ions are measured to be 3.6mm away from the beam axis and so can be completely eliminated by the slits. Isotopic ratios have been measured beyond these slits, and it is shown that these ratios are constant to better than half a percent using recent samples. The final strong focusing magnet has a rejection ratio for unwanted carbon ions greater than 107

  10. Solid Phase Microextraction and Miniature Time-of-Flight Mass Spectrometer

    Hiller, j.m.

    1999-01-26

    A miniature mass spectrometer, based on the time-of-flight principle, has been developed for the detection of chemical warfare agent precursor molecules. The instrument, with minor modifications, could fulfill many of the needs for sensing organic molecules in various Defense Programs, including Enhanced Surveillance. The basic footprint of the instrument is about that of a lunch box. The instrument has a mass range to about 300, has parts-per-trillion detection limits, and can return spectra in less than a second. The instrument can also detect permanent gases and is especially sensitive to hydrogen. In volume, the device could be manufactured for under $5000.