The CsCl/LiCl system has been studied for over a century now. Numerous phases have been predicted - only three have hitherto been found. We present the synthesis and single-crystal structure of the cesium lithium pentachloride CsLiCl, predicted earlier but with a different structure. The anhydrous new phase readily reacts to CsLiCl · 4HO in air. The tetrahydrate can also be obtained through the simplest, most inexpensive and green synthesis possible: an immediate, room-temperature mechanosynthesis from only CsCl and LiCl (3 : 1) in air. Differential scanning calorimetry (DSC) and thermogravimetric analyses (TGA), as well as temperature-dependent powder X-ray diffraction studies on this second ever reported ternary alkali chloride hydrate allowed for a revision of the CsCl/LiCl phase diagram. Density of states and total energy calculations further elucidate the new alkali chlorides and update the relative stability of previous structure predictions.
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http://dx.doi.org/10.1002/ejic.201900774 | DOI Listing |
Materials (Basel)
December 2024
Faculty of Chemical Technology and Engineering, Bydgoszcz University of Science and Technology, Seminaryjna 3, 85-326 Bydgoszcz, Poland.
The growing demand for alkali metals (AMs), such as lithium, cesium, and rubidium, related to their wide application across various industries (e.g., electronics, medicine, aerospace, etc.
View Article and Find Full Text PDFNat Commun
January 2025
Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Renmin Hospital of Wuhan University, Wuhan University, Wuhan, China.
Monovalent salts are generally believed to stabilize DNA duplex by weakening inter-strand electrostatic repulsion. Unexpectedly, our force-induced hairpin unzipping experiments and thermal melting experiments show that LiCl, NaCl, KCl, RbCl, and CsCl at concentrations beyond ~1 M destabilize DNA, RNA, and RNA-DNA duplexes. The two types of experiments yield different changes in free energy during melting, while the results that high concentration monovalent salts destabilize duplexes are common.
View Article and Find Full Text PDFSci Total Environ
December 2024
Xizang Bureau of Geology and Mineral Exploration and Development, Lhasa 850000, China.
High lithium (Li) and cesium (Cs) concentrations in the Qinghai-Xizang Plateau thermal springs pose environmental and health challenges, but their origins and enrichment mechanisms remain unclear. This study focuses on the Sogdoi geothermal field, located along the southern Karakoram Fault, to investigate these processes. Multi-isotope analyses (H, O, Li, Sr) reveal that Li and Cs predominantly originate from the host rocks, especially granitoids and meta-sedimentary rocks, rather than from magmatic fluids.
View Article and Find Full Text PDFSci Total Environ
December 2024
Dipartimento di Ingegneria, Università degli Studi di Palermo, viale delle Scienze ed. 6, 90128 Palermo, Italy.
Brine mining can represent a valuable non-conventional resource for the extraction of Mg, Li, B, Sr and other Trace Elements (TEs) such as Rb, Cs, whose recoveries require chemical reagents such as alkaline and acidic solutions. In a circular strategy, these required chemicals can be produced in-situ through Electrodialysis with Bipolar Membranes (EDBM). In this work, a laboratory EDBM unit was operated using real brines from Trapani saltworks to investigate, for the first time, the migration of minor and trace ions, as Li, B, Sr, Cs and Rb through ion-exchange membranes (IEMs).
View Article and Find Full Text PDFLangmuir
December 2024
ACA Berlin, Max-Planck-Str. 5, D-12489 Berlin, Germany.
This communication represents the chemical alternative to the previous two papers dealing with the influence of positively charged alkali cations on the adsorption properties of the series of the standard surfactant system of alkali-perfluorocarbon octanoates. Now, this contribution describes the adsorption properties of the negatively charged cationic surfactant series of trimethyldodecyl-ammonium halides. In our latest contributions, we have put forward a new model of adsorption of ionic surfactants.
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