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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 (P(D2)) and helium partial pressure (P(He)) could be obtained. The result shows that deuterium partial pressure could be measured if P(D2) > 10(-6) Pa (limited by ultimate pressure of calibration vessel), and helium pressure could be measured only if P(He)/P(D2) > 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.
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http://dx.doi.org/10.1063/1.4944560 | DOI Listing |
Horm Metab Res
September 2025
Clinical Biochemistry, The Royal Wolverhampton NHS Trust, Black Country Pathology Services, Wolverhampton, United Kingdom of Great Britain and Northern Ireland.
Parathyroid hormone (PTH) assays are not standardized and therefore PTH results are interpreted using manufacturer-provided assay-specific reference intervals. Assay-specific PTH reference intervals, however, do not account for between-assay differences and lead to discordance in the diagnosis of normocalcaemic primary hyperparathyroidism (NCPHPT). PTH increases with age independent of vitamin D, renal function, phosphate and ionized calcium.
View Article and Find Full Text PDFJ Antimicrob Chemother
September 2025
Department of Pharmaceutical Sciences, University of Michigan College of Pharmacy, Ann Arbor, MI 48109, USA.
Background: Synergy between antibiotic pairs is typically discovered using chequerboard assays that assume uniform, static drug exposure; however, such conditions rarely apply in vivo. Dynamic and heterogeneous tissue environments create spatial and temporal mismatches in drug exposure that can uncouple synergistic interactions, leading to unexpected treatment failure.
Objective: This study aims to develop a physiologically relevant in vitro model that integrates infection-site microenvironments and drug-specific pharmacokinetics.
J Am Soc Mass Spectrom
September 2025
School of Life Sciences, The Chinese University of Hong Kong, Sha Tin, N.T., Hong Kong, 999077.
Electrospray ionization (ESI)-mass spectrometry (MS) is a key platform for analyzing post-translationally modified proteins. With continuous advances in MS instruments and data analysis methods, top-down analysis of intact proteoforms has become highly feasible. To accurately quantify proteoforms with varying post-translational modifications (PTMs), the influence of PTMs on the ESI-MS detection efficiency must be considered.
View Article and Find Full Text PDFJ Phys Chem B
September 2025
Université de Lorraine, CNRS, GeoRessources, Nancy F-54000, France.
Quartz is among the most abundant minerals on Earth, but its surface chemistry under varying pH conditions remains not fully understood. In particular, the interplay between pH, amphoteric behavior, and water adsorption properties has been the subject of a long-standing debate. This study presents a comprehensive, multitechnique investigation into the pH-dependent interfacial chemistry of quartz.
View Article and Find Full Text PDFSoft Matter
September 2025
Department of Chemical Engineering, Louisiana State University, Baton Rouge, LA, 70803, USA.
Polyelectrolytes, macromolecules with ionizable groups, play a critical role in applications ranging from energy storage and drug delivery to adhesives, owing to their strong interactions with ionic solutes and water. Despite their widespread utility, an atomistic understanding of how polyelectrolytes interact with ions remains incomplete, limiting the ability to precisely control their conformation and functional properties. To bridge this knowledge gap, we conducted molecular dynamics simulations of two representative polyelectrolytes, poly(vinylbenzyl trimethylammonium chloride) (PVBTACl) and sodium polystyrene sulfonate (NaPSS), across varying salt concentrations.
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