Search results for "Ambient ionization"
showing 10 items of 13 documents
Characterization of oligomeric compounds in secondary organic aerosol using liquid chromatography coupled to electrospray ionization Fourier transfor…
2009
The components of secondary organic aerosols (SOAs) generated from the gas-phase ozonolysis of two C(10)H(16)-terpenes (alpha-pinene; sabinene) and a cyclic C(6)H(10) alkene (cyclohexene) were characterized by the use of a Fourier transform ion cyclotron mass spectrometer equipped with an electrospray ionization source operated in the negative ion mode. Reversed-phase high-performance liquid chromatography was used to achieve chromatographic separation of highly oxidized organic compounds. In addition to the well-known group of low molecular weight oxidation products (monomers; e.g. dicarboxylic acids), higher molecular weight compounds (dimers) were also detected and their exact elemental …
Determination of the first ionization potential of einsteinium by resonance ionization mass spectroscopy (RIMS)
1998
Abstract The first ionization potential of einsteinium (IP Es ) was determined by resonance ionization mass spectroscopy (RIMS) using samples with ≤10 12 atoms of 254 Es ( T 1/2 =276 days). This method is based on the measurement of photoionization thresholds as a function of applied electric field strength, followed by extrapolation to zero field strength to yield IP Es . An atomic beam of Es was created by heating a filament on which einsteinium was electrodeposited from an aqueous solution onto a tantalum backing and covered with titanium metal. Es atoms were ionized via a three-step excitation scheme, and the ions mass-selectively detected in a time-of-flight (TOF) mass spectrometer. Th…
Determination of the first ionization potential of nine actinide elements by resonance ionization mass spectroscopy (RIMS)
1998
The high sensitivity of RIMS enables the precise determination of the first ionization potential of actinide elements with a sample size of ≤1012 atoms. By multiple resonant laser excitation, the actinide atoms under investigation are ionized in the presence of an electric field, and the ions are mass-selectively detected in a time-of-flight spectrometer. The first ionization potential is obtained by scanning the wavelength of the laser used for the last excitation step across the ionization threshold Wth—indicated by a sudden increase of the ion count rate—at various electric field strengths. Extrapolation of Wth to electric field strength zero leads directly to the first ionization potent…
Critical assessment of ionization patterns and applications of ambient desorption/ionization mass spectrometry using FAPA-MS
2016
Ambient desorption/ionization mass spectrometry (MS) has gained growing interest during the last decade due to its high analytical performance and yet simplicity. Here, one of the recently developed ambient desorption/ionization MS sources, the flowing atmospheric-pressure afterglow (FAPA) source, was investigated in detail regarding background ions and typical ionization patterns in the positive as well as the negative ion mode for a variety of compound classes, comprising alkanes, alcohols, aldehydes, ketones, carboxylic acids, organic peroxides and alkaloids. A broad range of signals for adducts and losses was found, besides the usually emphasized detection of quasimolecular ions, i.e. […
A new interface to couple thin-layer chromatography with laser desorption/atmospheric pressure chemical ionization mass spectrometry for plate scanni…
2005
An interface to allow on-line qualitative and quantitative full-plate detection and analysis of compounds separated by thin-layer chromatography (TLC) is presented. A continuous wave diode laser is employed as a desorption source. Atmospheric pressure chemical ionization mass spectrometry ionizes and subsequently identifies the desorbed sample molecules. Besides direct laser desorption on untreated TLC plates, graphite particles were used as a matrix to couple in the laser power and improve the efficiency of desorption.
Measurement of nanoparticle mass distributions by laser desorption/ionization time-of-flight mass spectrometry.
2011
In this paper, access to the mass distribution analysis of nanoparticles is described based on laser desorption/ionization and time of flight mass spectrometry. Two examples are given, demonstrating the accurate mass distribution analysis of nanoparticles fabricated both ex situ and in situ during the laser-assisted desorption process. The potentials and the limitations of the method are discussed, with special emphasis on carbonaceous clusters and molecules.
Use of Ambient Ionization High-Resolution Mass Spectrometry for the Kinetic Analysis of Organic Surface Reactions
2016
In contrast to homogeneous systems, studying the kinetics of organic reactions on solid surfaces remains a difficult task due to the limited availability of appropriate analysis techniques that are general, high-throughput, and capable of offering quantitative, structural surface information. Here, we demonstrate how direct analysis in real time mass spectrometry (DART-MS) complies with above considerations and can be used for determining interfacial kinetic parameters. The presented approach is based on the use of a MS tag that - in principle - allows application to other reactions. To show the potential of DART-MS, we selected the widely applied strain-promoted alkyne-azide cycloaddition …
Study of short-lived tin isotopes with a laser ion source
1995
A chemically selective laser ion source based on resonance ionization of atoms in a hot cavity has been applied for the study of short-lived silver isotopes at CERN/ ISOLDE. Silver atoms were ionized by two resonant excitations and final laser ionization into the continuum. Decay properties of the neutron-rich isotopes121–127Ag were studied with a neutron long-counter and aβ-detector.
A laser ion source for trace analysis
1988
A laser ion source has been set up which is based on resonant stepwise excitation and ionization of atomic vapor confined in an ionization chamber. Using a pulsed copper vapor/dye laser system with a high repetition rate (6.5 kHz) one expects high efficiency and high selectivity for this new type of ion source. First test experiments with lead are reported.
Production of negative osmium ions by laser desorption and ionization.
2010
The interest to produce negative osmium ions is manifold in the realm of high-accuracy ion trap experiments: high-resolution nearly Doppler-free laser spectroscopy, antihydrogen formation in its ground state, and contributions to neutrino mass spectrometry. Production of these ions is generally accomplished by sputtering an Os sample with Cs(+) ions at tens of keV. Though this is a well-established method commonly used at accelerators, these kind of sources are quite demanding and tricky to operate. Therefore, the development of a more straightforward and cost effective production scheme will be of benefit for ion trap and other experiments. Such a scheme makes use of desorption and ionizat…