The technique of proton transfer reaction mass spectrometry (PTR-MS) couples a proton transfer reagent, usually H3O+, with a drift tube and mass spectrometer to determine concentrations of volatile organic compounds. Here we describe a first attempt to use chemical ionization (CI) reagents other than proton transfer species inside a PTR-MS instrument. The ability to switch to other types of CI reagents provides an extra dimension to the technique. This capability is demonstrated by focusing on the ability to distinguish several isobaric aldehydes and ketones, including the atmospherically important molecules methacrolein and methyl vinyl ketone. Two CI reagents were selected, H3O+ and NO+, both being cleanly generated in a low intensity radioactive source prior to injection into the drift tube. By recording spectra with both of these reagents, the contributions from different isobaric molecules can be separated by virtue of their unique spectrometric 'fingerprints'. The work demonstrates that this form of instrumentation is not restricted to proton transfer reagents and is the basis of a more general technique, chemical ionization reaction mass spectrometry (CIRMS).
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/rcm.2202 | DOI Listing |
Langmuir
January 2025
National Key Laboratory of Oil and Gas Reservoir Geology and Exploitation, Southwest Petroleum University, Chengdu 610500, P. R. China.
To balance the stability and dissolution of polyacrylamide (PAM), emulsion drag reducers dominate the successful operation of volumetric fracturing. Herein, a pH-switchable four-tailed ionic liquid surfactant (OA/Cyclen) is synthesized by oleic acid (OA) and 1,4,7,10-tetraazacyclododecane (Cyclen). The four-tailed structure of OA/Cyclen enhances the stability of the emulsion polymerization reactor and supplies enough switchable sites for triggering the intensified release of the PAM emulsion.
View Article and Find Full Text PDFSensors (Basel)
December 2024
Institute of Autmatic Control, University of Kaiserslautern-Landau, 67653 Kaiserslautern, Germany.
Harsh operating conditions imposed by vehicular applications significantly limit the utilization of proton exchange membrane fuel cells (PEMFCs) in electric propulsion systems. Improper/poor management and supervision of rapidly varying current demands can lead to undesired electrochemical reactions and critical cell failures. Among other failures, flooding and catalytic degradation are failure mechanisms that directly impact the composition of the membrane electrode assembly and can cause irreversible cell performance deterioration.
View Article and Find Full Text PDFPolymers (Basel)
December 2024
Department of Organic and Polymer Chemistry, College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, China.
Stimulus-responsive luminescent materials are pivotal in the field of sensing. Fluorescent transition metal complexes with a charge transfer excited state, especially terpyridine-coordinated polymers, are of particular interest due to their tunable emission. In this paper, a novel bis-terpyridine ligand was synthesized and assembled into a coordination polymer, which showed intense visible light absorption and fluorescence emission in the solid state that could be regulated by an acidic or basic pH.
View Article and Find Full Text PDFMolecules
December 2024
Institute of Resources and Environmental Engineering, Shanxi University, Taiyuan 030032, China.
The real-time measurement of the content of impurities such as iron and aluminium ions is one of the keys to quality evaluation in the production process of high-purity lithium carbonate; however, impurity detection has been a time-consuming process for many years, which limits the optimisation of the production of high-purity lithium carbonate. In this context, this work explores the possibility of using water-soluble fluorescent probes for the rapid detection of impurity ions. Salicylaldehyde was modified with the hydrophilic group dl-alanine to synthesise a water-soluble Al fluorescent probe (Probe A).
View Article and Find Full Text PDFMolecules
December 2024
Departamento de Química, Universidad Autónoma de Madrid, Cantoblanco, 28049 Madrid, Spain.
Ab initio calculations of cross sections for electron capture by protons in collisions with CO are carried out at energies between 100 eV/u and 50 keV/u, employing a semiclassical method within the Franck-Condon framework. The scattering wave function is expanded in a set of ab initio electronic wave functions of the HCO supermolecule. The calculation is performed on several trajectory orientations to obtain orientation-averaged total cross sections.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!