Printed circuit board (PCB) based drift tube ion mobility spectrometers enable the use of state-of-the-art production techniques to manufacture compact devices with excellent performance at minimum cost. The new PCB ion mobility spectrometer (PCB-IMS) presented here is equipped with either a 140 MBq tritium or a 95 MBq nickel-63 ionization source and consists of a combination of horizontally arranged 6-layer PCBs for the drift and reaction regions and vertically arranged PCBs for interfacing the ionization source, ion shutter, and detector. The design allows the reproducible manufacturing and thus comparison of different IMS topologies. Here, we investigate different ion shutters, field-switching, Bradbury-Nielsen, and tristate and their effects on resolving power and limits of detection considering two different ionization region geometries and ionization sources, tritium and nickel-63. It is shown that the high resolving power of > 80 at low drift voltage of 3 kV and short drift length of 50 mm can be achieved independent of the used ion shutter mechanism and reaction region geometry. While the resolving power of all ion shutters is excellent, the Bradbury-Nielsen shutter shows a pronounced discrimination of slow ion species when using short shutter opening times for small initial ion cloud widths, as required for high resolving power. Thus, the intensity of the proton-bound dimer of 2-pentanone is reduced by 30% compared to the signal intensity obtained with both the field-switching and tristate shutter. The detection limits employing the Bradbury-Nielsen shutter and a 50 mm reaction region as required for nickel-63 are 58 ppt for the protonated monomer and 3.4 ppb for the proton-bound dimer of 2-pentanone. The detection limits achieved with the tristate shutter utilizing the same reaction region are slightly higher for the protonated monomer at 68 ppt, but lower for the proton-bound dimer at 2 ppb due to the advanced ion shutter principle not discriminating slow ions. However, the lowest detection limits of 13 ppt and 301 ppt can be achieved with the field-switching shutter and a 2 mm reaction region, sufficient for a tritium ionization source.
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http://dx.doi.org/10.1021/acs.analchem.0c04140 | DOI Listing |
Gels
December 2024
Universidad de Buenos Aires, Facultad de Farmacia y Bioquímica, Departamento de Ciencias Químicas, Ciudad Autónoma de Buenos Aires 1113, Argentina.
In this work, the mechanical properties of hydrogels based on linear polyethyleneimine (PEI) chemically crosslinked with ethyleneglycoldiglycidyl ether (EGDE) were improved by the ionic crosslinking with sodium tripolyphosphate (TPP). To this end, the quaternization of the nitrogen atoms present in the PEI structure was conducted to render a network with a permanent positive charge to interact with the negative charges of TPP. The co-crosslinking process was studied by H high-resolution magic angle spinning (H HRMAS) NMR and X-ray photoelectron spectroscopy (XPS) in combination with organic elemental analysis and inductively coupled plasma mass spectrometry (ICP-MS).
View Article and Find Full Text PDFEnergy Environ Sci
December 2024
Department of Physics, University of Oxford, Clarendon Laboratory Oxford OX1 3PU UK
It is widely accepted that mobile ions are responsible for the slow electronic responses observed in metal halide perovskite-based optoelectronic devices, and strongly influence long-term operational stability. Electrical characterisation methods mostly observe complex indirect effects of ions on bulk/interface recombination, struggle to quantify the ion density and mobility, and are typically not able to fully quantify the influence of the ions upon the bulk and interfacial electric fields. We analyse the bias-assisted charge extraction (BACE) method for the case of a screened bulk electric field, and introduce a new characterisation method based on BACE, termed ion drift BACE.
View Article and Find Full Text PDFJ Adv Res
December 2024
College of Agronomy and Biotechnology, China Agricultural University/ The Innovation Center (Beijing) of Crop Seeds Whole-Process Technology Research of Ministry of Agriculture and Rural Affairs/ Beijing Key Laboratory of Crop Genetic Improvement, Beijing 100193, China. Electronic address:
Food Chem
December 2024
School of Life Science, Jiangxi Science &Technology Normal University, Nanchang 330013, China.
In this study, the dynamic effects of ultrasonic treatment (0-400 W) on the volatile flavor compounds of pumpkin juice under different storage periods were investigated systematically using a combination of headspace solid-phase microextraction gas chromatography-mass spectrometry (HS-SPME-GC-MS) and gas chromatography-ion mobility spectrometry (GC-IMS) techniques. A total of 139 and 46 volatile organic compounds (VOCs) were identified by GC-MS and GC-IMS, respectively. The results indicated that complex changes in volatile components occurred during storage.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Organocatalysis Research Group, Institute of Organic Chemistry, HUN-REN Research Centre for Natural Sciences, Magyar tudósok körútja 2, Budapest H-1117, Hungary.
The partial reduction of esters to aldehydes is a fundamentally important transformation for the synthesis of numerous fine chemicals and consumer goods. However, despite the many efforts, limitations have persisted, such as competing overreduction, low reproducibility, use of exigent reaction conditions and hazardous chemicals. Here, we report a novel catalyst family with a unique steric design which promotes the catalytic partial reduction of esters with unprecedented, near-perfect selectivity and efficiency.
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