A Simple Scan- and Display-Control for Magnetic Sector Mass Spectrometers

Abstract

Magnetically scanned sector mass spectrometers yield excellent spectra, covering a wide mass range. The spectral display is most reproducible if the magnet is cycled continuously in order to establish a constant hysteresis history.

We have adapted a single sweep spectrometer to continuous cycling. A simple and flexible control initiates and times the magnetic up- and down-sweep, erases and triggers a storage oscilloscope, advances and arrests the photographic recording chart and actuates an event marker on the recorder of the associated gas chromatograph.     

Gas Flow in the Capillary of the Atmosphere-to-Vacuum Interface of Mass Spectrometers

Numerical simulations of a gas flow through a capillary being a part of mass spectrometer atmospheric interface were performed using a detailed laminar flow model. The simulated interface consisted of atmospheric and forevacuum volumes connected via a thin capillary. The pressure in the forevacuum volume where the gas was expanding after passing through the capillary was varied in the wide range from 10 to 900 mbar in order to study the volume flow rate as well as the other flow parameters as functions of the pressure drop between the atmospheric and forevacuum volumes. The capillary wall temperature was varied in the range from 24 to 150 °C. Numerical integration of the complete system of Navier-Stokes equations for a viscous compressible gas taking into account the heat transfer was performed using the standard gas dynamic simulation software package ANSYS CFX. The simulation results were compared with experimental measurements of gas flow parameters both performed using our experimental setup and taken from the literature. The simulated volume flow rates through the capillary differed no more than by 10% from the measured ones over the entire pressure and temperatures ranges. A conclusion was drawn that the detailed digital laminar model is able to quantitatively describe the measured gas flow rates through the capillaries under conditions considered.

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High-Speed MALDI-TOF Imaging Mass Spectrometry: Rapid Ion Image Acquisition and Considerations for Next Generation Instrumentation

A prototype matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometer has been used for high-speed ion image acquisition. The instrument incorporates a Nd:YLF solid state laser capable of pulse repetition rates up to 5 kHz and continuous laser raster sampling for high-throughput data collection. Lipid ion images of a sagittal rat brain tissue section were collected in 10 min with an effective acquisition rate of roughly 30 pixels/s. These results represent more than a 10-fold increase in throughput compared with current commercially available instrumentation. Experiments aimed at improving conditions for continuous laser raster sampling for imaging are reported, highlighting proper laser repetition rates and stage velocities to avoid signal degradation from significant oversampling. As new high spatial resolution and large sample area applications present themselves, the development of high-speed microprobe MALDI imaging mass spectrometry is essential to meet the needs of those seeking new technologies for rapid molecular imaging.     

Experimental Characterization of Secular Frequency Scanning in Ion Trap Mass Spectrometers

Secular frequency scanning is implemented and characterized using both a benchtop linear ion trap and a miniature rectilinear ion trap mass spectrometer. Separation of tetraalkylammonium ions and those from a mass calibration mixture and from a pesticide mixture is demonstrated with peak widths approaching unit resolution for optimized conditions using the benchtop ion trap. The effects on the spectra of ion trap operating parameters, including waveform amplitude, scan direction, scan rate, and pressure are explored, and peaks at black holes corresponding to nonlinear (higher-order field) resonance points are investigated. Reverse frequency sweeps (increasing mass) on the Mini 12 are shown to result in significantly higher ion ejection efficiency and superior resolution than forward frequency sweeps that decrement mass. This result is accounted for by the asymmetry in ion energy absorption profiles as a function of AC frequency and the shift in ion secular frequency at higher amplitudes in the trap due to higher order fields. We also found that use of higher AC amplitudes in forward frequency sweeps biases ions toward ejection at points of higher order parametric resonance, despite using only dipolar excitation. Higher AC amplitudes also increase peak width and decrease sensitivity in both forward and reverse frequency sweeps. Higher sensitivity and resolution were obtained at higher trap pressures in the secular frequency scan, in contrast to conventional resonance ejection scans, which showed the opposite trend in resolution on the Mini 12. Mass range is shown to be naturally extended in secular frequency scanning when ejecting ions by sweeping the AC waveform through low frequencies, a method which is similar, but arguably superior, to the more usual method of mass range extension using low q resonance ejection.

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Addition of Nucleophiles to Fragment Ions in Mass Spectrometers under Electrospray-Ionization Conditions

Mass spectra of several aromatic compounds containing an amino or thiol group were recorded under electrospray conditions with a Finnigan TSQ 700, as well as on a Bruker Esquire-LC spectrometer. The MS/MS spectra displayed two main peaks: the first one arising from the cleavage of the amino or thiol group; the second one appeared at 18 Da higher than the first one. It could be shown that the second peak resulted from a nucleophilic addition of one water molecule to the fragment ion.     

Homolytic Reactive Mass Spectrometry of Fullerenes: Peculiarities of the Reactions of C60 with Aromatic Compounds in the Ionization Chambers of Mass Spectrometers and in Solution

C₆₀ reacted with PhH, PhCl, BnH, BnNH₂, and o-C₂H₂B₁₀H₁₀ in the electron impact (EI) ion source of a mass spectrometer at 300 °C forming phenyl, benzyl, and o-carboranyl adducts, respectively, stabilized by hydrogen addition and loss. Besides, the additions to C₆₀ of methyl and phenyl radicals for toluene, and a phenyl radical for benzylamine were observed. A homolytic reaction mechanism was suggested involving the reaction of the radicals formed from the aromatics under EI with C₆₀ at the ionization chamber walls. While the ion/molecule reaction of C₆₀ with benzene performed by Sun et al. under chemical ionization conditions at 200 °C afforded the complex C₆₀?PhH^+?, quite a different isomer, HC₆₀Ph^+?, was detected in the present study as a sequence of the different reaction mechanisms. C₆₀ also reacted with benzyl bromide in the laser desorption/ionization (LDI) source of a mass spectrometer to give C₆₀CPh⁺. Phenyl and benzyl derivatives of C₆₀ were found, respectively, when the reactions of the fullerene with PhCl, BnH, and BnBr were performed in solution under ultra violet irradiation. For the reaction with toluene, the strong chemically induced dynamic electron polarization of the intermediate benzylfullerenyl radical with the reverse phase effect was found. The coincidence of the results of the mass spectrometry and solution reactions of C₆₀ with aromatics, even though incomplete, additionally supports the hypothesis, formulated earlier, that the former results can predict the latter ones to a significant extent and shows that this conclusion is valid for both EI and LDI initiated reactions in mass spectrometers.      

Cold Active Pectinases: Advancing the Food Industry to the Next Generation

Pectinase has been an integral part of commercial food processing, where it is used for degradation of pectin and facilitates different processing steps such as liquefaction, clarification and juice extraction. The industry currently uses pectinases from mesophilic or thermophilic microorganisms which are well established, but recently, there has been is a new trend in the food industry to adopt low-temperature processing. This trend is due to the potential economic and environmental advantages which the industry envisages. In order to achieve this change, an alternative for the existing pectinases, which are mostly mesophilic and temperature-dependent, must be identified, which can function efficiently at low temperatures. Psychrophilic pectinases derived from cold-adapted microorganisms, are known to function at low to freezing temperatures and may be an alternative to address the problem. Psychrophilic pectinases can be obtained from the vast microflora inhabiting various cold regions on earth such as oceans, Polar Regions, snow-covered mountains, and glaciers. This article is intended to study the advantages of cold active pectinases, its sources, and the current state of the research.     

Comparison of Triple Quadrupole and Double Focusing Mass Spectrometers to Investigate Collision-Induced Dissociation and Metastable Ions of Glycoconjugates

Glycoconjugates, such as chromophore-labeled disaccharides and permethylated glycosphingolipids (GSL) were used for comparison of triple quadrupole and double focusing mass spectrometers in analysis of product ions. A profound effect of collision energy was observed in the product ion spectra of ceramide ions (fragment ions of permethylated GSL): more product ions were observed from a double focusing mass spectrometer. Besides collision energy, the structure of the analyte had a significant effect on the formation of product ions. Despite the fact that masses of protonated molecular ions (MH⁺) of permethylated GSL are significantly larger than their ceramide fragments, the low-energy and high-energy product ion spectra of MH⁺ are, in general, similar. In a double focusing mass spectrometer of reversed geometry, more metastable ions were observed in the first field free region (FFR) than in the second FFR. The metastable ions observed in the second FFR were similar to those observed in low-energy collision-induced dissociation (CID). Although a double focusing mass spectrometer is superior to triple quadrupole instrument for detection of product ions, the poor resolution in either the selection of precursor ion or in the product ion spectra can be a serious problem in analysis of a mixture with similar masses.     

Olefins and Vinyl Polar Monomers: Bridging the Gap for Next Generation Materials

The inherent differences in reactivity between activated and non‐activated alkenes prevents copolymerization using established polymer synthesis techniques. Research over the past 20 years has greatly advanced the copolymerization of polar vinyl monomers and olefins. This Review highlights the challenges associated with conventional polymerization systems and evaluates the most relevant methods which have been developed to “bridge the gap” between polar vinyl monomers and olefins. We discuss advancements in heteroatom tolerant coordination–insertion polymerizations, methods of controlling radical polymerizations to incorporate olefinic monomers, as well as combined approaches employing sequential polymerizations. Finally, we discuss state‐of‐the‐art stimuli‐responsive systems capable of facile switching between catalytic pathways and provide an outlook towards applications in which tailored copolymers are ideally suited.     

DNA Architectonics: towards the Next Generation of Bio‐inspired Materials

The use of DNA in nanobiotechnology has advanced to a stage at which almost any two or three dimensional architecture can be designed with high precision. The choice of the DNA sequences is essential for successful self‐assembly, and opens new ways of making nanosized monomolecular assemblies with predictable structure and size. The inclusion of designer nucleoside analogues further adds functionality with addressable groups, which have an influence on the function of the DNA nano‐objects. This article highlights the recent achievements in this emerging field and gives an outlook on future perspectives and applications.     

臭氧的应用及产生技术

主要阐述了臭氧的性质、用途及产生技术,并重点介绍了臭氧的用途和臭氧产生技术的现状。     

The Design of a Next Generation Force Field: The X-POL Potential

An electronic structure-based polarization method, called the X-POL potential, has been described for the purpose of constructing an empirical force field for modeling polypeptides. In the X-POL potential, the internal, bonded interactions are fully represented by an electronic structure theory augmented with some empirical torsional terms. Non-bonded interactions are modeled by an iterative, combined quantum mechanical and molecular mechanical method, in which the molecular mechanical partial charges are derived from the molecular wave functions of the individual fragments. In this paper, the feasibility of such an electronic structure force field is illustrated by small model compounds. A method has been developed for separating a polypeptide chain into peptide units and its parameterization procedure in the X-POL potential is documented and tested on glycine dipeptide. We envision that the next generation of force fields for biomolecular polymer simulations will be developed based on electronic structure theory, which can adequately define and treat many-body polarization and charge delocalization effects.     

Self‐Cleaning and Next Generation Anti‐Fog Surfaces and Coatings

Due to their high surface energy, hydrophilic surfaces are susceptible to contaminations which are difficult to remove and often ruin the surface. Traditional anti‐fog coatings are especially limited by contaminants, as the prevention of fogging is enhanced as hydrophilicity increases. Thus, advanced solutions to fogging are required which incorporate some degree of self‐cleaning ability without significant losses in anti‐fog character. Potential next generation anti‐fog surfaces are characterized with particular emphasis on extended lifetime stimuli‐responsive surfaces. Surfactant‐based surfaces exhibited simultaneous hydrophilicity, necessary for anti‐fogging, and oleophobicity, necessary for contamination resistance. The combination of these features rendered the surface as self‐cleaning.

     

TEMPO-Assisted Free Radical-Initiated Peptide Sequencing Mass Spectrometry (FRIPS MS) in Q-TOF and Orbitrap Mass Spectrometers: Single-Step Peptide Backbone Dissociations in Positive Ion Mode

The present study demonstrates that one-step peptide backbone fragmentations can be achieved using the TEMPO [2-(2,2,6,6-tetramethyl piperidine-1-oxyl)]-assisted free radical-initiated peptide sequencing (FRIPS) mass spectrometry in a hybrid quadrupole time-of-flight (Q-TOF) mass spectrometer and a Q-Exactive Orbitrap instrument in positive ion mode, in contrast to two-step peptide fragmentation in an ion-trap mass spectrometer (reference Anal. Chem. 85, 7044–7051 (30)). In the hybrid Q-TOF and Q-Exactive instruments, higher collisional energies can be applied to the target peptides, compared with the low collisional energies applied by the ion-trap instrument. The higher energy deposition and the additional multiple collisions in the collision cell in both instruments appear to result in one-step peptide backbone dissociations in positive ion mode. This new finding clearly demonstrates that the TEMPO-assisted FRIPS approach is a very useful tool in peptide mass spectrometry research.

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Organic Supercapacitors as the Next Generation Energy Storage Device: Emergence,Opportunity, and Challenges

Harnessing new materials for developing high-energy storage devices set off research in the field of organic supercapacitors. Various attractive properties like high energy density, lower device weight, excellent cycling stability, and impressive pseudocapacitive nature make organic supercapacitors suitable candidates for high-end storage device applications. This review highlights the overall progress and future of organic supercapacitors. Sustainable energy production and storage depend on low cost, large supercapacitor packs with high energy density. Organic supercapacitors with high pseudocapacitance, lightweight form factor, and higher device potential are alternatives to other energy storage devices. There are many recent ongoing research works that focus on organic electrolytes along with the material aspect of organic supercapacitors. This review summarizes the current research status and the chemistry behind the storage mechanism in organic supercapacitors to overcome the challenges and achieve superior performance for future opportunities.     

职责与生成：群众路线的政治逻辑研究

马克思主义认为,代替资产阶级统治的必将是人民统治,即群众管理国家。但是由于群众自身的管理能力问题,需要有一个政治力量来带领群众前进,引导群众管理国家事务,这个政治力量就是共产党。共产党的职责就是引导群众管理国家,克服群众管理国家的障碍。共产党要完成自身的职责,就要密切联系群众,尊重群众的主体地位,坚持群众路线。因而群众路线与共产党履行自身职责使命具有内在相关性。共产党践行群众路线,既要发挥政党主体功能,深入群众,开展调查研究,满足群众需求,教育提升群众,又要把群众首创经验上升为党的政策,群众路线的实现需要共产党与群众双方共同努力,因而群众路线又是一个不断生成的过程。     

Simulation of Duty Cycle-Based Trapping and Ejection of Massive Ions Using Linear Digital Quadrupoles: the Enabling Technology for High Resolution Time-of-Flight Mass Spectrometry in the Ultra High Mass Range

Duty cycle-based trapping and extraction processes have been investigated for linear digitally-driven multipoles by simulating ion trajectories. The duty cycles of the applied waveforms were adjusted so that an effective trapping or ejection electric field was created between the rods and the grounded end cap electrodes. By manipulating the duty cycles of the waveforms, the potentials of the multipole rods can be set equal for part of the waveform cycle. When all rods are negative for this period, the device traps positive ions and when all are positive, it ejects them in focused trajectories. Four Linac II electrodes[1] have been added between the quadrupole rods along the asymptotes to create an electric field along the symmetry axis for collecting the ions near the exit end cap electrode and prompt ejection. This method permits the ions to be collected and then ejected in a concentrated and collimated plug into the acceleration region of a time-of-flight mass spectrometer (TOFMS). Our method has been shown to be independent of mass. Because the resolution of orthogonal acceleration TOFMS depends primarily on the dispersion of the ions injected into the acceleration region and not on the ion mass, this technology will enable high resolution in the ultrahigh mass range (m/z > 20,000).     

数字化矩形离子阱质谱仪的设计及性能

将数字化离子阱技术和矩形离子阱(RIT)技术相结合,建立了数字化矩形离子阱质谱仪.此技术和装置既具有数字化电源的结构简单、输出稳定和易精确控制等特点,又结合了矩形离子阱的高离子存储效率、结构简单以及加工和装配容易等优点.构建了基于电喷雾(ESI)电离源的数字化矩形离子阱质谱仪系统,并使用Fenfluramine和PPG2000分别对此系统的质量分辨率和质量范围进行了测试.研究结果表明:一个用印刷线路板(PCB)制作的简单矩形离子阱,在200 V(半峰值)的数字束缚电压的驱动下,获得了大于500的质量分辨率和超过2600 Th的质量范围.实验证明,数字化离子阱技术的应用可以显著提高矩形离子阱的性能,特别是质量范围等关键的质谱仪指标.     

Generation of Supraclusters and Nanoclusters Using Laser Desorption/Ionisation Mass Spectrometry

Laser desorption/ionisation of discrete molecular clusters combined with time-of-flight (TOF) or Fourier-transform ion cyclotron resonance (FTICR) mass spectrometry affords spectra in which extensive higher mass clusters are observed. The size of the largest cluster aggregates (or supraclusters) is of the same order of magnitude as nanoclusters. The spectra obtained using TOF mass spectrometry sometimes exhibit post-source decay fragmentation, depending upon the operational conditions employed during data acquisition, which, although providing useful data on the ligand dissociation dynamics, complicate spectral interpretation. Complementary FTICR mass spectra are free of such features. The identities of the supra/nanoclusters generated from the molecular cluster precursors have not been conclusively established but are mostly coordinatively unsaturated. Density functional molecular orbital calculations have identified the possible structures of the comparatively simple electronically unsaturated system, [Ru₃(CO)₆]^–, that provides a clue to the aggregation mechanism.