Vapour state intercalation of alkali metals into polyparaphenylene: ESR study

1996 ◽  
Vol 57 (6-8) ◽  
pp. 1141-1144 ◽  
Author(s):  
M. Sebti ◽  
J. Ghanbaja ◽  
A. Merlin ◽  
D. Billaud
Keyword(s):  

It has been uncertain until recently, whether any of the many intermetallic compounds which have been established in liquid and solid alloys can persist into the vapour state, or whether they invariably dissociate into mere mixtures of the individual metal vapours. Volatile compounds have occasionally been suspected ( e. g ., between magnesium and zinc) on account of the deposition of typical crystals of compounds during the distillation of an alloy of the two metals, but such evidence is so indirect that it carries little weight. The most promising way of approaching this question is by a study of the absorption spectra of mixtures of metallic vapours. The metals that are known to possess a measurable proportion of diatomic or polyatomic molecules in the vapour state invariably indicate this property by the appearance of bands in their absorption spectra. In fact, since it has been accepted that band spectra cannot originate from single atoms, the observation of such bands has become the most delicate test for the existence of association in the vapours. For example, the usual methods of molecular weight determination have led to the belief that the alkali metal vapours are solely monatomic. This cannot, however, be true, as each of these metals possesses an extensive band spectrum, which appears at quite low vapour pressures. There can be no doubt, on the basis of this spectroscopic evidence, that an appreciable fraction of the molecules in the vapour of boiling sodium, etc., are di- (or poly-) atomic. This point will be discussed fully below.


2020 ◽  
Author(s):  
Lucas A. Freeman ◽  
Akachukwu D. Obi ◽  
Haleigh R. Machost ◽  
Andrew Molino ◽  
Asa W. Nichols ◽  
...  

The reduction of the relatively inert carbon–oxygen bonds of CO<sub>2</sub> to access useful CO<sub>2</sub>-derived organic products is one of the most important fundamental challenges in synthetic chemistry. Facilitating this bond-cleavage using earth-abundant, non-toxic main group elements (MGEs) is especially arduous because of the difficulty in achieving strong inner-sphere interactions between CO<sub>2</sub> and the MGE. Herein we report the first successful chemical reduction of CO<sub>2</sub> at room temperature by alkali metals, promoted by a cyclic(alkyl)(amino) carbene (CAAC). One-electron reduction of CAAC-CO<sub>2</sub> adduct (<b>1</b>) with lithium, sodium or potassium metal yields stable monoanionic radicals clusters [M(CAAC–CO<sub>2</sub>)]<sub>n</sub>(M = Li, Na, K, <b> 2</b>-<b>4</b>) and two-electron alkali metal reduction affords open-shell, dianionic clusters of the general formula [M<sub>2</sub>(CAAC–CO<sub>2</sub>)]<sub>n </sub>(<b>5</b>-<b>8</b>). It is notable that these crystalline clusters of reduced CO<sub>2</sub> may also be isolated via the “one-pot” reaction of free CO<sub>2</sub> with free CAAC followed by the addition of alkali metals – a reductive process which does not occur in the absence of carbene. Each of the products <b>2</b>-<b>8</b> were investigated using a combination of experimental and theoretical methods.<br>


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Lilla Fijołek ◽  
Joanna Świetlik ◽  
Marcin Frankowski

AbstractIn water treatment technology, activated carbons are used primarily as sorbents to remove organic impurities, mainly natural organic matter, but also as catalysts in the ozonation process. Commercially available activated carbons are usually contaminated with mineral substances, classified into two main groups: alkali metals (Ca, Na, K, Li, Mg) and multivalent metals (Al, Fe, Ti, Si). The presence of impurities on the carbon surface significantly affects the pHpzc values determined for raw and ozonated carbon as well as their acidity and alkalinity. The scale of the observed changes strongly depends on the pH of the ozonated system, which is related to the diffusion of impurities from the carbon to the solution. In an acidic environment (pH 2.5 in this work), the ozone molecule is relatively stable, yet active carbon causes its decomposition. This is the first report that indirectly indicates that contaminants on the surface of activated carbon (multivalent elements) contribute to the breakdown of ozone towards radicals, while the process of ozone decomposition by purified carbons does not follow the radical path in bulk solution. Carbon impurities also change the distribution of the reaction products formed by organic pollutants ozonation, which additionally confirms the radical process. The study showed that the use of unpurified activated carbon in the ozonation of succinic acid (SA) leads to the formation of a relatively large amount of oxalic acid (OA), which is a product of radical SA degradation. On the other hand, in solutions with purified carbon, the amount of OA generated is negligible.


2021 ◽  
Vol 13 (2) ◽  
pp. 2584-2599
Author(s):  
Anetta Platek-Mielczarek ◽  
Cristina Nita ◽  
Camélia Matei Ghimbeu ◽  
Elzbieta Frackowiak ◽  
Krzysztof Fic

2021 ◽  
Vol 60 (3) ◽  
pp. 1948-1956
Author(s):  
Lyudmila A. Lapkina ◽  
Anna A. Sinelshchikova ◽  
Kirill P. Birin ◽  
Vladimir E. Larchenko ◽  
Mikhail S. Grigoriev ◽  
...  

2021 ◽  
Author(s):  
Ahmed H Biby ◽  
Basant A. Ali ◽  
Nageh Allam

Intercalation of alkali metals has proved to be an effective approach for the enhancement of the energy storage performance in layered-2D materials. However, the research so far has been limited...


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