Continuous ion separation via electrokinetic-driven ion migration path differentiation: Practical application to lithium extraction from brines

2022 ◽  
Author(s):  
Geunbae Lim ◽  
Hyukjin Jean Kwon ◽  
Minsoo Lee ◽  
Woochul Jung
Keyword(s):  
Chemical Properties ◽  
Practical Application ◽  
Ion Migration ◽  
Migration Path ◽  
Ion Separation ◽  
Effective Separation ◽  
Similar Chemical

The effective separation of Mg2+ from Li+ is the key for realizing efficient and economic lithium extraction from brine, but remains challenging due to their similar chemical properties. Recent approaches...

scholarly journals Shellfish Chitosan Potential in Wine Clarification

2021 ◽  
Vol 11 (10) ◽  
pp. 4417
Author(s):  
Veronica Vendramin ◽  
Gaia Spinato ◽  
Simone Vincenzi
Keyword(s):  
Molecular Structure ◽  
Chemical Properties ◽  
Allergic Reactions ◽  
Chitin Content ◽  
Deacetylation Degree ◽  
Physical Chemical ◽  
Similar Chemical ◽  
Fungal Chitosan ◽  
Significant Difference ◽  
Fish Industry

Chitosan is a chitin-derived fiber, extracted from the shellfish shells, a by-product of the fish industry, or from fungi grown in bioreactors. In oenology, it is used for the control of Brettanomyces spp., for the prevention of ferric, copper, and protein casse and for clarification. The International Organisation of Vine and Wine established the exclusive utilization of fungal chitosan to avoid the eventuality of allergic reactions. This work focuses on the differences between two chitosan categories, fungal and animal chitosan, characterizing several samples in terms of chitin content and degree of deacetylation. In addition, different acids were used to dissolve chitosans, and their effect on viscosity and on the efficacy in wine clarification were observed. The results demonstrated that even if fungal and animal chitosans shared similar chemical properties (deacetylation degree and chitin content), they showed different viscosity depending on their molecular weight but also on the acid used to dissolve them. A significant difference was discovered on their fining properties, as animal chitosans showed a faster and greater sedimentation compared to the fungal ones, independently from the acid used for their dissolution. This suggests that physical–chemical differences in the molecular structure occur between the two chitosan categories and that this significantly affects their technologic (oenological) properties.

Group III-Sb Metamorphic Buffer on Si for p-Channel all-III-V CMOS: Electrical Properties, Growth and Surface Defects

2015 ◽  
Vol 1790 ◽  
pp. 13-18
Author(s):  
Shun Sasaki ◽  
Shailesh Madisetti ◽  
Vadim Tokranov ◽  
Michael Yakimov ◽  
Makoto Hirayama ◽  
...  
Keyword(s):  
Surface Defects ◽  
Lattice Mismatch ◽  
Chemical Properties ◽  
Antiphase Domain ◽  
Hole Transport ◽  
Heteroepitaxial Growth ◽  
Group Iii ◽  
Similar Chemical ◽  
Unintentional Doping ◽  
P Type

ABSTRACTGroup III-Sb compound semiconductors are promising materials for future CMOS circuits. Especially, In1-xGaxSb is considered as a complimentary p-type channel material to n-type In1-xGaxAs MOSFET due to the superior hole transport properties and similar chemical properties in III-Sb’s to those of InGaAs. The heteroepitaxial growth of In1-xGaxSb on Si substrate has significant advantage for volume fabrication of III-V ICs. However large lattice mismatch between InGaSb and Si results in many growth-related defects (micro twins, threading dislocations and antiphase domain boundaries); these defects also act as deep acceptor levels. Accordingly, unintentional doping in InGaSb films causes additional scattering, increase junction leakages and affects the interface properties. In this paper, we studied the correlations between of defects and hole carrier densities in GaSb and strained In1-xGaxSb quantum well layers by using various designs of metamorphic superlattice buffers.

Diamonds are Forever and Zirconium is for Submarines

2013 ◽  
Author(s):  
Lars Öhrström
Keyword(s):  
Transition Metals ◽  
Periodic Table ◽  
Chemical Properties ◽  
Pure Metal ◽  
Cubic Zirconia ◽  
Love Story ◽  
Zirconium Silicate ◽  
Similar Chemical ◽  
Engagement Rings

The appearance of a diamond engagement ring in the long and convoluted love story between Botswana’s First Lady Detective, Mma Ramotswe, and the owner and brilliant mechanic of Tlokweng Road Speedy Motors, Mr J. L. B. Matekoni, seems to signal an end to this particular sub-plot, stretching over several volumes of Alexander McCall Smith’s bestselling and original series of crime novels (that we met in Chapter 1). However, a slight problem involving cubic zirconia is discovered, and the story lingers on until the next book in the series. Similar names for elements and their compounds are a nuisance in chemistry, but oft en arise historically, and zirconium is just one such example. Apart from the pure metal we have zircon and zirconia, all three of which have important applications. Zircon is zirconium silicate, with the formula ZrSiO4, and cubic zirconia is a special form of zirconium dioxide, ZrO2. The latter, as you may have guessed, is an excellent diamond substitute in, among other applications, engagement rings. We are not going to dwell on the details of the element zirconium, but you should know that within the Periodic Table it is located in the large middle chunk called the transition metals. You have probably heard of its cousin titanium, immediately above it, and a sibling, hafnium, straight down the ladder. Why do I call them siblings? Because in the Periodic Table elements in the same column tend to have similar chemical properties. In particular, in the family of transition metals in the central section containing 27 elements—each with a number of properties in common—the two lower elements in each column tend to be the most similar. The similar chemical properties of zirconium and titanium means that we can usually find zirconium where we mine the much more plentiful titanium, and also that once we have separated the titanium from zirconium there will be a small quantity of hafnium trailing along—an impurity that is much harder to get rid of. The sleek jeweller in Gaborone will not care if his fake diamonds contain trace levels of HfO2 mixed with the ZrO2.

Analytical Methodology from Lavoisier to Mendeleev

2014 ◽  
Author(s):  
Marco Fontani ◽  
Mariagrazia Costa ◽  
Mary Virginia Orna
Keyword(s):  
Chemical Change ◽  
Chemical Properties ◽  
Professional Activity ◽  
Analytical Methodology ◽  
Long Run ◽  
Similar Chemical ◽  
Experimental Errors ◽  
Ancient Times ◽  
Almost All ◽  
Physical And Chemical

Within the period covered by Part II, 1789–1869, 37 true elements, almost all of them metals, were discovered. Prior to this time, about 14 metals had been discovered, excluding those that had been known from ancient times. The discovery of the elements during this period of interest is intimately related to the analytical methodologies available to chemists, as well as to a growing consciousness of just what an element is. Because these methods were also available to the less competent who may have lacked the skills to use them or the knowledge to interpret their results, their use also led to as many, if not more, erroneous discoveries in the same period. One can number among the major sources of error faulty interpretation of experimental data, the “rediscovery” of an already known element, sample impurities, very similar chemical properties (as in the case of the rare earths), the presence of an element in nature in very scarce or trace amounts, gross experimental errors, confusion of oxides and earths with their metals, and baseless dogmatic pronouncements by known “authorities” in the field. Antoine Laurent Lavoisier’s conceptualization of what constitutes an element was a radical break from the principles of alchemy. His stipulation that an element is a substance that cannot be further decomposed conferred an operational, pragmatic, concrete definition on what had previously been a more abstract concept. At the other end of the spectrum was the intuition of Dmitri Mendeleev who, contrary to the prevailing acceptance of Lavoisier’s concept, stressed the importance of retaining a more abstract, more fundamental sense of an element—an idea that in the long run enabled the development of the periodic table. What both men had in common is that they defined and named individual elements as those components of substances that could survive chemical change and whose presence in compounds could explain their physical and chemical properties. Mendeleev’s table has been immortalized in every chemistry classroom—and also concretely in Saint Petersburg, the city that saw most of his professional activity, by a spectacular building-sized model The analytical chemist depends on both of these concepts and indeed, analytical practice preceded Lavoisier’s concept by at least a century.

Energy Dispersive X-Ray Fluorescence (EDXRF) Analysis as a Reliable Nondestructive Industrial Tool

1979 ◽  
Vol 23 ◽  
pp. 157-161
Author(s):  
L. E. Miller ◽  
H. J. Abplanalp
Keyword(s):  
Alloy Composition ◽  
Chemical Properties ◽  
Nondestructive Analysis ◽  
Destructive Testing ◽  
Roughness Effects ◽  
Destructive Sampling ◽  
X Ray ◽  
The Past ◽  
Edxrf Analysis ◽  
Similar Chemical

For the past several years the Boeing Aerospace Company has been implementing advanced nondestructive chemical analysis methods to improve product reliability and reduce material inspection costs. Previous testing of incoming material for conformance to vendor test reports or of production materials for verification of alloy composition, had consisted of either time-consuming destructive testing or nondestructive chemical spot testing, which often was insensitive to differences between alloys of similar chemical properties. Beginning in 1974, development of EDXRF techniques was initiated to provide a rapid nondestructive analysis capability for both laboratory and factory use. For materials containing elements easily excited by EDXRF methods, costly destructive sampling and testing can be avoided. Generally, chips, wire, barstock, sheet or plate can be analyzed using an annular radioactive source. The uniformity of the X-ray flux diminishes sample geometry and surface roughness effects.

Using Electron Energy-Loss Spectroscopy (EELS) To Study Rare Earth Elements In Natural Crystals

2000 ◽  
Vol 6 (S2) ◽  
pp. 206-207
Author(s):  
Huifang Xu
Keyword(s):  
Rare Earth ◽  
Energy Loss ◽  
Rare Earth Elements ◽  
Electron Energy ◽  
Energy Resolution ◽  
Electron Energy Loss Spectroscopy ◽  
Relative Concentration ◽  
Chemical Properties ◽  
Similar Chemical ◽  
Electron Energy Loss

Because of similar chemical properties of the rare earth elements (Ree), whole series of the Ree may occur in natural Ree-bearing crystals. Relative concentration of the Ree may vary as the crystallization environments change. Electron energy-dispersive spectroscopy (EDS) associated with TEM is unable to resolve Ree and other coexistence elements, such as Ba nd Ti, because of peak overlap and energy resolution (∼ 150 eV) of EDS. Figure A indicate multiple peaks from Ce only. The Cu peaks are from Cu grid holding the specimen. Electron energy-loss spectroscopy (EELS) with energy resolution of < 1 eV is able to resolve all Ree in natural Ree-bearing crystals.Natural carbonate crystals from a Ree ore deposit were investigated by using EELS associated with field emission-gun (FEG) TEM. The crystals are in a chemical series of BaCO3 - Ree(CO3)F [1]. In Figure B, EEL spectra A and B are from Ce-rich and La-rich bastnaesite (Ree(CO3)F), respectively; spectrum D is from cordylite (BaCO3 (Ree(CO3)F); spectrum E is from huanghoite (BaCO3 Ree(CO3)F), spectrum F is from BaCO3; spectrum C is from an unknown Ree-rich phase.

scholarly journals Cellulose Nanofibers Preparation from Cassava Peels via Mechanical Disruption

Fibers ◽  
2019 ◽  
Vol 7 (5) ◽  
pp. 44
Author(s):  
Sonny Widiarto ◽  
Edi Pramono ◽  
Suharso ◽  
Achmad Rochliadi ◽  
I Made Arcana
Keyword(s):  
Physical Properties ◽  
Acid Hydrolysis ◽  
Alkali Treatment ◽  
Cellulose Nanofibers ◽  
Chemical Properties ◽  
Bleaching Process ◽  
Mechanical Disruption ◽  
Similar Chemical ◽  
Cassava Peels

In this study, cellulose and cellulose nanofibers (CNF) were extracted and prepared from cassava peels (CPs). The method of the cellulose extraction was performed by alkali treatment followed by a bleaching process. The CNF were prepared by mechanical disruption procedure (homogenization and ultrasonication), and the results were compared with a common acid hydrolysis procedure. The resulting cellulose and CNF from both procedures were then analyzed using FTIR, SEM, TEM, XRD, and TGA. The results show that cellulose and CNF were successfully prepared from both procedures. The physical properties of the produced CNF were different; however, they had similar chemical properties.

scholarly journals Basidiomycotic Yeast Cryptococcus diffluens Converts l-Galactonic Acid to the Compound on the Similar Metabolic Pathway in Ascomycetes

Fermentation ◽  
2019 ◽  
Vol 5 (3) ◽  
pp. 73
Author(s):  
Matsubara ◽  
Kataoka ◽  
Kishida
Keyword(s):  
Galacturonic Acid ◽  
High Performance ◽  
Chemical Properties ◽  
Value Added ◽  
Anion Exchange Chromatography ◽  
Exchange Chromatography ◽  
Conversion Process ◽  
Nuclear Magnetic Resonance Analysis ◽  
Resonance Analysis ◽  
Similar Chemical

(1) Background: It has been shown that d-galacturonic acid is converted to l-galactonic acid by the basidiomycotic yeast, Cryptococcus diffluens. However, two pathways are hypothesized for the l-galactonic acid conversion process in C. diffluens. One is similar to the conversion process of the filamentous fungi in d-galacturonic acid metabolism and another is the conversion process to l-ascorbic acid, reported in the related yeast, C. laurentii. It is necessary to determine which, if either, process occurs in C. diffluens in order to produce novel value-added products from d-galacturonic acid using yeast strains. (2) Methods: The diethylaminoethy (DEAE)-fractionated enzyme was prepared from the cell-free extract of C. diffluens by the DEAE column chromatography. The l-galactonic acid conversion activity was assayed using DEAE-fractionated enzyme and the converted product was detected and fractionated by high-performance anion-exchange chromatography. Then, the molecular structure was identified by nuclear magnetic resonance analysis. (3) Results: The product showed similar chemical properties to 2-keto-3-deoxy-l-galactonic acid (l-threo-3-deoxy-hexulosonic acid). (4) Conclusions: It is suggested that l-galactonic acid is converted to 2-keto-3-deoxy-l-galactonic acid by dehydratase in C. diffluens. The l-galactonic acid conversion process of C. diffluens is a prioritized pathway, similar to the pathway of ascomycetes.

Reliable organic memristors for neuromorphic computing by predefining a localized ion-migration path in crosslinkable polymer

Nanoscale ◽  
2020 ◽  
Vol 12 (44) ◽  
pp. 22502-22510
Author(s):  
Hea-Lim Park ◽  
Min-Hwi Kim ◽  
Min-Hoi Kim ◽  
Sin-Hyung Lee
Keyword(s):  
Neuromorphic Computing ◽  
Ion Migration ◽  
Migration Path ◽  
Novel Concept

A novel concept for confining filament growth in an organic memristor is demonstrated by exploiting the functionality of crosslinkable polymers.

scholarly journals Understanding Collaborative Effects between the Polymer Gel Structure and the Applied Electrical Field in Gel Electrophoresis Separation

2019 ◽  
Vol 2019 ◽  
pp. 1-15 ◽  
Author(s):  
Jennifer A. Pascal ◽  
Koteswara Rao Medidhi ◽  
Mario A. Oyanader ◽  
Holly A. Stretz ◽  
Pedro E. Arce
Keyword(s):  
Gel Electrophoresis ◽  
Chemical Properties ◽  
Polymer Gels ◽  
Optimal Time ◽  
Polymer Gel ◽  
Gel Structure ◽  
Electrical Field ◽  
Standard Case ◽  
Similar Chemical ◽  
Applied Electrical Field

The collaborative effects between an applied orthogonal electrical field and the internal structure of polymer gels in gel electrophoresis is studied by using microscopic-based electrophoretic transport models that then are upscaled via the format of electro kinetics-hydrodynamics (EKHD). The interplay of the electrical field and internal gel morphology could impact the separation of biomolecules that, because of similar chemical properties, are usually difficult to separate. In this study, we focus on an irregular pore geometry of the polymer-gel structure by using an axially varying pore (i.e., an axially divergent section) and an orthogonal (to the main flow of solutes) applied electrical field. The microscopic-based conservation of species equation is formulated for the standard case of electrophoresis of charged particles within a geometrical domain, i.e., a pore, and upscaled to obtain macroscopic-based diffusion and mobility coefficients. These coefficients are then used in the calculation of the optimal time of separation to study the effect of the varying parameters of the pore structure under different values of the electrical field. The results are qualitatively consistent with those reported, in the literature, by using computational-based approaches as well as with experiments also reported in the literature, previously. The study shows the important collaborative effects between the applied electrical field and the internal geometry of the polymer gels that could lead to improving biomolecule separation in gel electrophoresis.

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