Changes in electrical resistance (delta R), water (delta H2O), and blood variables (Na+, K+, Cl-, protein [Pr], osmolality [Osmo], hemoglobin [Hb], and hematocrit [Hct]) were monitored during hemodialysis in 20 subjects. Average delta H2O was 1.69 +/- 0.91 liters. Blood, R, and circumferences (C) were measured for the upper limb (UL), lower limb (LL), and total body (TB) before, midway, and at the end of dialysis. Segmental volumes (V) and specific resistivity (rho) were computed. delta Hct and delta Pr were stronger predictors of delta H2O than delta R. Forward stepwise regression analysis using delta R at 5, 50, and 548 kHz, delta Pr, and delta Hct showed that delta Hct and delta Pr alone accounted for 77% of the variance in delta TBW. Adding delta R increased this at most to 81%. Both the UL and LL had significant increases in rho. The volumetric change of the UL was nonsignificant, whereas that of the LL accounted for over one half of the delta H2O. Single frequency bioimpedance cannot be used to monitor dialytic delta H2O unless one accounts for fluid composition changes. Monitoring bioimpedance changes over only a single body segment is also questioned.
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http://dx.doi.org/10.1097/00002480-199307000-00089 | DOI Listing |
Nat Commun
January 2025
Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory of Rare Earth Materials Chemistry and Applications, PKU-HKU Joint Laboratory in Rare Earth Materials and Bioinorganic Chemistry, College of Chemistry and Molecular Engineering, Peking University, Beijing, China.
Dual active sites with synergistic valence state regulation under oxidizing and reducing conditions are essential for catalytic reactions with step-wise mechanisms to modulate the complex adsorption sites of reactant molecules on the surfaces of heterogeneous catalysts with maximized catalytic performances, but it has been rarely explored. In this work, uniformly dispersed CuCo alloy and CoO nanosheet composite catalysts with dual active sites are constructed, which shows huge boost in activity for catalyzing water-gas shift reaction (WGSR), with a record high reaction rate reaching 204.2 μmol g s at 300 °C for CuCoO amongst the reported Cu-based and Co-based catalysts.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
The Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi 214122, China.
Electrocatalytic nitrate reduction to ammonia (eNRA) is a promising route toward environmental sustainability and clean energy. However, its efficiency is often limited by the slow conversion of intermediates due to spin-forbidden processes. Here, we introduce a novel A-site high-entropy strategy to develop a new perovskite oxide (LaPrNdBaSr)CoO (LPNBSC) for eNRA.
View Article and Find Full Text PDFDalton Trans
January 2025
State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemical Engineering, Nanjing Tech University, Nanjing 211816, P. R. China.
In the history of magnetochemistry development, lanthanide-transition (3d-4f) heterometallic compounds have been considered an attractive candidate for magnetic refrigerants. Herein, a series of heterometallic compounds have been designed and templated by CO anions, that is, {[LnNi(L)(CO)(HO)]·HO} [Ln = Gd (. Gd2Ni) = Sm (.
View Article and Find Full Text PDFNanomaterials (Basel)
December 2024
Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education, School of Materials Science and Engineering, Institutes of Physical Science and Information Technology, Anhui University, Hefei 230601, China.
Cryogenic magnetic refrigerants based on the magnetocaloric effect (MCE) hold significant potential as substitutes for the expensive and scarce He-3. Gd(III)-based complexes are considered excellent candidates for low-temperature magnetic refrigerants. We have synthesized a series of Ln(III)-based metal-organic framework (MOF) (Ln = Gd/Dy) by the slow release of oxalates in situ from organic ligands (disodium edetate dehydrate (EDTA-2Na) and thiodiglycolic acid).
View Article and Find Full Text PDFInorg Chem
January 2025
School of Science and Technology, Nottingham Trent University, Nottingham, Clifton Lane NG11 8NS, U.K.
We report the synthesis of three radical-cation salts of BEDT-TTF from racemic tris(oxalato)ferrate by electrocrystallization in the presence of chiral molecules. In the presence of enantiopure l-(+)-tartaric acid, we observe spontaneous resolution of the labile tris(oxalato)ferrate anion to produce the chiral radical-cation salt α-(BEDT-TTF)[Δ-Fe(CO)].[l-(+)-tartaric acid] which contains only the Δ enantiomer of Fe(CO).
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