Intercalation of heavy alkali metals (K, Rb and Cs) in the bundles of single wall nanotubes

2000 ◽  
Author(s):  
L. Duclaux
2021 ◽  
Vol 23 (1) ◽  
pp. 219-228
Author(s):  
Nabanita Saikia ◽  
Mohamed Taha ◽  
Ravindra Pandey

The rational design of self-assembled nanobio-molecular hybrids of peptide nucleic acids with single-wall nanotubes rely on understanding how biomolecules recognize and mediate intermolecular interactions with the nanomaterial's surface.


Author(s):  
S. A. Lurie ◽  
Yu. O. Solyaev ◽  
Ya. I. Estrin ◽  
E. R. Badamshina ◽  
G. S. Kulagina

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 11 (1) ◽  
Author(s):  
Muhammad Bilal ◽  
Hamna Arshad ◽  
Muhammad Ramzan ◽  
Zahir Shah ◽  
Poom Kumam

AbstractThe key objective of the present research is to examine the hybrid magnetohydrodynamics (MHD) nanofluid (Carbon-nanotubes and ferrous oxide–water) CNT–Fe3O4/H2 flow into a horizontal parallel channel with thermal radiation through squeezing and dilating porous walls. The parting motion is triggered by the porous walls of the channel. The fluid flow is time-dependent and laminar. The channel is asymmetric and the upper and lower walls are distinct in temperature and are porous. With the combination of nanoparticles of Fe3O4 and single and multi-wall carbon nanotubes, the hybrid nanofluid principle is exploited. By using the similarity transformation, the set of partial differential equations (PDEs) of this mathematical model, governed by momentum and energy equations, is reduced to corresponding ordinary differential equations (ODEs). A very simple numerical approach called the Runge–Kutta system of order four along with the shooting technique is used to achieve the solutions for regulating ODEs. MATLAB computing software is used to create temperature and velocity profile graphs for various emerging parameters. At the end of the manuscript, the main conclusions are summarized. Through different graphs, it is observed that hybrid-nanofluid has more prominent thermal enhancement than simple nanofluid. Further, the single-wall nanotubes have dominated impact on temperature than the multi-wall carbon nanotubes. From the calculations, it is also noted that Fe2O3–MWCNT–water has an average of 4.84% more rate of heat transfer than the Fe2O3–SWCNT–water. On the other hand, 8.27% more heat flow observed in Fe2O3–SWCNT–water than the simple nanofluid. Such study is very important in coolant circulation, inter-body fluid transportation, aerospace engineering, and industrial cleaning procedures, etc.


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