scholarly journals Examining the Deliquescence of Lithium Salts and Those of Other Alkali Metals Through a Range of Humidity

2021 ◽  
Vol 7 (2) ◽  
pp. 90
Author(s):  
Charles Allen ◽  
Ivanescu Andrew ◽  
Justus Lee

It is well known that lithium chloride is able to extract moisture from the ambient air. Our research in this area has examined a variety of lithium salts for their ability to do so, as well as their counterparts containing sodium and potassium. Additionally, we have made and utilized chambers that allow us to examine deliquescence of these salts in conditions of various humidity. We will present the results, and how these experiments can be adapted to the teaching of laboratory courses.

2020 ◽  
Vol 2020 ◽  
pp. 1-7
Author(s):  
Kuanysh Samarkhanov ◽  
Mendykhan Khasenov ◽  
Erlan Batyrbekov ◽  
Inesh Kenzhina ◽  
Yerzhan Sapatayev ◽  
...  

The luminescence of Kr-Xe, Ar-Kr, and Ar-Xe mixtures was studied in the spectral range 300–970 nm when excited by 6Li (n, α)3 H nuclear reaction products in the core of a nuclear reactor. Lithium was deposited on walls of experimental cell in the form of a capillary-porous structure, which made it possible to measure up to a temperature of 730 K. The temperature dependence of the radiation intensity of noble gas atoms, alkali metals, and heteronuclear ionic noble gas molecules was studied. Also, as in the case of single-component gases, the appearance of lithium lines and impurities of sodium and potassium is associated with vaporization during the release of nuclear reaction products from the lithium layer. The excitation of lithium atoms occurs mainly as a result of the Penning process of lithium atoms on noble gas atoms in the 1s states and subsequent ion-molecular reactions. Simultaneous radiation at transitions of atoms of noble gases and lithium, heteronuclear ion molecules of noble gases allows us to increase the efficiency of direct conversion of nuclear energy into light.


1970 ◽  
Vol 16 (2) ◽  
pp. 139-143 ◽  
Author(s):  
John Pybus ◽  
George N Bowers

Abstract Lithium concentrations in the serum of patients undergoing therapy with lithium salts were measured by atomic absorption spectroscopy. Serum was diluted 10-fold with water. Physiological amounts of sodium and potassium were included in the blank and standard solutions because these cations enhance the lithium signal by 2%. Calcium, magnesium, bicarbonate, sulfate, and phosphate at the concentrations found in serum were without effect. Protein clogging of the triple-slot Boling burner was not observed. The relative standard deviation of within-run variability was 0.6% (n = 20 and x = 0.88 mEq/liter), and of daily precision, tested over a month, it was 2.5% (n = 30, x = 0.91 mEq/liter). Recovery of 1.00 mEq of lithium added per liter of serum ranged from 97 to 103%, averaging 99.8%.


2002 ◽  
Vol 85 (3) ◽  
pp. 219-241 ◽  
Author(s):  
Peter J. Cragg

Transport of alkali metals, particularly sodium and potassium, across cell membranes is an essential function performed by special proteins that enable cells to regulate inter- and extracellular ion concentrations with exceptional selectivity. The importance of these channel-forming proteins has led to researchers emulating of their structural features: an ion-specific filter and conduction at rates up to 108 ions per second. Synthetic helical and cyclic polypeptides form channels, however, the specificity of ion transport is often low. Ion-specific macrocycles have been used as filters from which membrane-spanning derivatives have been prepared. Success has been limited as many compounds act as ion carriers rather than forming transmembrane channels. Surfactant compounds also allow ions to cross membranes but any specificity is serendipitous. Overall it seems possible to mimic either ion specificity or efficient transmembrane ion transport. The goal for the future will be to combine both characteristics in one artificial system.


Author(s):  
Pietro Cremaschi ◽  
Aldo Gamba ◽  
Gabriele Morosi ◽  
Cesare Oliva ◽  
Massimo Simonetta

1953 ◽  
Vol 26 (3) ◽  
pp. 543-558
Author(s):  
Avery A. Morton ◽  
Frank H. Bolton ◽  
Frances W. Collins ◽  
Edward F. Cluff

Abstract The alfin catalyst is a combination of sodium salts which causes butadiene to polymerize at extreme rapidity in such a fashion that a greater difference exists between sodium and alfin polymerization than between sodium and emulsion polymerization. Hitherto the combination has been assumed to be binary—allylsodium and sodium isopropoxide—but a new method of preparation has revealed that a halide or pseudohalide salt is essential. Chloride, bromide, and iodide salts of sodium and potassium can be used as the halide component, but fluoride and lithium salts, as a rule, cannot be so employed unless the small size of each ion is compensated by a large cation or anion, respectively, as found in cesium fluoride or lithium iodide. The sodium cation is required for the catalyst. The potassium ion can be tolerated in the alkoxide or halide, but not simultaneousely in both. The lithium ion is in general unsuitable. Alfin polybutadiene is differentiated from sodium-polymerized butadiene by a high proportion of 1,4-structure and by an abnormally high intrinsic viscosity. Iodine chloride causes the polymer to precipitate from solution. All results indicate that polymerization by sodium reagents is in considerable degree controlled by the association of other salts with the sodium reagent.


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