scholarly journals Synthesis and Dissolution of Metal Oxides in Ionic Liquids and Deep Eutectic Solvents

Molecules ◽  
2019 ◽  
Vol 25 (1) ◽  
pp. 78 ◽  
Author(s):  
Janine Richter ◽  
Michael Ruck
Keyword(s):  
Ionic Liquids ◽  
Low Temperature ◽  
Metal Oxide ◽  
Metal Oxides ◽  
High Temperatures ◽  
Deep Eutectic Solvents ◽  
Wide Range ◽  
Oxide Phases

Ionic liquids (ILs) and deep eutectic solvents (DESs) have proven to be suitable solvents and reactants for low-temperature reactions. To date, several attempts were made to apply this promising class of materials to metal oxide chemistry, which, conventionally, is performed at high temperatures. This review gives an overview about the scientific approaches of the synthesis as well as the dissolution of metal oxides in ILs and DESs. A wide range of metal oxides along with numerous ILs and DESs are covered by this research. With ILs and DESs being involved, many metal oxide phases as well as different particle morphologies were obtained by means of relatively simple reactions paths. By the development of acidic task-specific ILs and DESs, even difficultly soluble metal oxides were dissolved and, hence, made accessible for downstream chemistry. Especially the role of ILs in these reactions is in the focus of discussion.

Prebiotic studies on the interaction of zirconia nanoparticles and ribose nucleotides and their role in chemical evolution

2021 ◽  
Vol 20 (2) ◽  
pp. 142-149
Author(s):  
Avnish Kumar Arora ◽  
Pankaj Kumar
Keyword(s):  
Electron Microscopy ◽  
Metal Oxide ◽  
Metal Oxides ◽  
Chemical Evolution ◽  
Ribonucleic Acid ◽  
Zirconium Oxide ◽  
Origins Of Life ◽  
Neutral Ph ◽  
Interaction Studies

AbstractStudies on the interaction of biomolecules with inorganic compounds, mainly mineral surfaces, are of great concern in identifying their role in chemical evolution and origins of life. Metal oxides are the major constituents of earth and earth-like planets. Hence, studies on the interaction of biomolecules with these minerals are the point of concern for the study of the emergence of life on different planets. Zirconium oxide is one of the metal oxides present in earth's crust as it is a part of several types of rocks found in sandy areas such as beaches and riverbeds, e.g. pebbles of baddeleyite. Different metal oxides have been studied for their role in chemical evolution but no studies have been reported about the role of zirconium oxide in chemical evolution and origins of life. Therefore, studies were carried out on the interaction of ribonucleic acid constituents, 5′-CMP (cytidine monophosphate), 5′-UMP (uridine monophosphate), 5′-GMP (guanosine monophosphate) and 5′-AMP (adenosine monophosphate), with zirconium oxide. Synthesized zirconium oxide particles were characterized by using vibrating sample magnetometer, X-Ray Diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy. Zirconia particles were in the nanometre range, from 14 to 27 nm. The interaction of zirconium oxide with ribonucleic acid constituents was performed in the concentration range of 5 × 10−5–300 × 10−5 M. Interaction studies were carried out in three mediums; acidic (pH 4.0), neutral (pH 7.0) and basic (pH 9.0). At neutral pH, maximum interaction was observed. The interaction of zirconium oxide with 5′-UMP was 49.45% and with 5′-CMP 67.98%, while with others it was in between. Interaction studies were Langmurian in nature. Xm and KL values were calculated. Infrared spectral studies of ribonucleotides, metal oxide and ribonucleotide–metal oxide adducts were carried out to find out the interactive sites. It was observed that the nitrogen base and phosphate moiety of ribonucleotides interact with the positive charge surface of metal oxide. SEM was also carried out to study the adsorption. The results of the present study favour the important role of zirconium oxide in concentrating the organic molecules from their dilute aqueous solutions in primeval seas.

scholarly journals Role of salicylic acid in acclimation to low temperature

2013 ◽  
Vol 61 (2) ◽  
pp. 161-172 ◽  
Author(s):  
M. Pál ◽  
O. Gondor ◽  
T. Janda
Keyword(s):  
Salicylic Acid ◽  
Low Temperature ◽  
Plant Species ◽  
Membrane Integrity ◽  
Stress Factors ◽  
Limiting Factors ◽  
Wide Range ◽  
Metabolic Reactions ◽  
Related Compounds

Low temperature is one of the most important limiting factors for plant growth throughout the world. Exposure to low temperature may cause various phenotypic and physiological symptoms, and may result in oxidative stress, leading to loss of membrane integrity and to the impairment of photosynthesis and general metabolic processes. Salicylic acid (SA), a phenolic compound produced by a wide range of plant species, may participate in many physiological and metabolic reactions in plants. It has been shown that exogenous SA may provide protection against low temperature injury in various plant species, while various stress factors may also modify the synthesis and metabolism of SA. In the present review, recent results on the effects of SA and related compounds in processes leading to acclimation to low temperatures will be discussed.

scholarly journals CO Oxidation over Metal Oxide (La2O3, Fe2O3, PrO2, Sm2O3, and MnO2) Doped CuO-Based Catalysts Supported on Mesoporous Ce0.8Zr0.2O2 with Intensified Low-Temperature Activity

Catalysts ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 724 ◽  
Author(s):  
Yan Cui ◽  
Leilei Xu ◽  
Mindong Chen ◽  
Chufei Lv ◽  
Xinbo Lian ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Low Temperature ◽  
Metal Oxide ◽  
Metal Oxides ◽  
Co Oxidation ◽  
Active Sites ◽  
Earth Metal ◽  
High Dispersion ◽  
Impregnation Method ◽  
X Ray

CuO-based catalysts are usually used for CO oxidation owing to their low cost and excellent catalytic activities. In this study, a series of metal oxide (La2O3, Fe2O3, PrO2, Sm2O3, and MnO2)-doped CuO-based catalysts with mesoporous Ce0.8Zr0.2O2 support were simply prepared by the incipient impregnation method and used directly as catalysts for CO catalytic oxidation. These mesoporous catalysts were systematically characterized by X-ray powder diffraction (XRD), N2 physisorption, transmission electron microscopy (TEM), energy-dispersed spectroscopy (EDS) mapping, X-ray photoelectron spectroscopy (XPS), and H2 temperature programmed reduction (H2-TPR). It was found that the CuO and the dopants were highly dispersed among the mesoporous framework via the incipient impregnation method, and the strong metal framework interaction had been formed. The effects of the types of the dopants and the loading amounts of the dopants on the low-temperature catalytic performances were carefully studied. It was concluded that doped transition metal oxides could regulate the oxygen mobility and reduction ability of catalysts, further improving the catalytic activity. It was also found that the high dispersion of rare earth metal oxides (PrO2, Sm2O3) was able to prevent the thermal sintering and aggregation of CuO-based catalysts during the process of calcination. In addition, their presence also evidently improved the reducibility and significantly reduced the particle size of the CuO active sites for CO oxidation. The results demonstrated that the 15CuO-3Fe2O3/M-Ce80Zr20 catalyst with 3 wt. % of Fe2O3 showed the best low-temperature catalytic activity toward CO oxidation. Overall, the present Fe2O3-doped CuO-based catalysts with mesoporous nanocrystalline Ce0.8Zr0.2O2 solid solution as support were considered a promising series of catalysts for low-temperature CO oxidation.

Tuning metal oxide defect chemistry by thermochemical quenching

2020 ◽  
Vol 22 (11) ◽  
pp. 6308-6317
Author(s):  
Shehab Shousha ◽  
Sarah Khalil ◽  
Mostafa Youssef
Keyword(s):  
Low Temperature ◽  
Metal Oxide ◽  
Metal Oxides ◽  
First Principles ◽  
Growth Conditions ◽  
Defect Chemistry ◽  
First Principles Calculations

Based on first-principles calculations, we show how to tune the low temperature defect chemistry of metal oxides by varying growth conditions.

scholarly journals Nanocrystalline Metal Oxides for Methane Sensors: Role of Noble Metals

2009 ◽  
Vol 2009 ◽  
pp. 1-20 ◽  
Author(s):  
S. Basu ◽  
P. K. Basu
Keyword(s):  
Metal Oxide ◽  
Metal Oxides ◽  
Noble Metal ◽  
Gas Sensors ◽  
Noble Metals ◽  
Industrial Applications ◽  
Metal Catalyst ◽  
Nanocrystalline Metal ◽  
Sensing Properties

Methane is an important gas for domestic and industrial applications and its source is mainly coalmines. Since methane is extremely inflammable in the coalmine atmosphere, it is essential to develop a reliable and relatively inexpensive chemical gas sensor to detect this inflammable gas below its explosion amount in air. The metal oxides have been proved to be potential materials for the development of commercial gas sensors. The functional properties of the metal oxide-based gas sensors can be improved not only by tailoring the crystal size of metal oxides but also by incorporating the noble metal catalyst on nanocrystalline metal oxide matrix. It was observed that the surface modification of nanocrystalline metal oxide thin films by noble metal sensitizers and the use of a noble metal catalytic contact as electrode reduce the operating temperatures appreciably and improve the sensing properties. This review article concentrates on the nanocrystalline metal oxide methane sensors and the role of noble metals on the sensing properties.

scholarly journals The effect of metal oxide on the cure, morphology, thermal and mechanical characteristics of chloroprene and butadiene rubber blends

2019 ◽  
Vol 77 (8) ◽  
pp. 4131-4146 ◽  
Author(s):  
Aleksandra Smejda-Krzewicka ◽  
Anna Olejnik ◽  
Krzysztof Strzelec
Keyword(s):  
Metal Oxide ◽  
Metal Oxides ◽  
Cross Linking ◽  
Butadiene Rubber ◽  
Rubber Blends ◽  
Chloroprene Rubber ◽  
Index Value ◽  
Positive Effect ◽  
Very High

Abstract This paper discusses the role of metal oxides (MeO) in the cross-linking process and useful properties of chloroprene and butadiene rubber (CR/BR) blends. Iron(III) oxide (Fe2O3), iron(II,III) oxide (Fe3O4), silver(I) oxide (Ag2O) or zinc oxide were used. It has found that every proposed metal oxide can be used as a cross-linking agent of the CR/BR blends. The degree of cross-linking was evaluated by means of vulcametric parameters, equilibrium swelling in selected solvents and Mooney–Rivlin elasticity constants. The properties of the cured CR/BR products, such as tensile strength, stress at elongation, tension set under constant elongation and compression set, were also investigated. The results revealed that all CR/BR/MeO vulcanizates were characterized by a high cross-linking degree and satisfying mechanical properties. The most important advantage of obtained rubber goods is very high resistance to flame. The increase in the oxygen index value for the CR/BR/Fe2O3, CR/BR/Fe3O4 and CR/BR/Ag2O vulcanizates compared to the standard cross-linked chloroprene rubber showed that presented metal oxides provided a positive effect on the resistance to flame of the new CR/BR/MeO composites. Satisfactory properties of the studied blends are related to the presence of the interelastomer bonding of both rubbers in the compositions.

scholarly journals The Key Role of Active Sites in the Development of Selective Metal Oxide Sensor Materials

Sensors ◽  
2021 ◽  
Vol 21 (7) ◽  
pp. 2554
Author(s):  
Artem Marikutsa ◽  
Marina Rumyantseva ◽  
Elizaveta A. Konstantinova ◽  
Alexander Gaskov
Keyword(s):  
Metal Oxide ◽  
Metal Oxides ◽  
Active Sites ◽  
Noble Metals ◽  
Material Composition ◽  
Mixed Metal Oxides ◽  
Mixed Metal ◽  
Sensor Materials ◽  
The Impact

Development of sensor materials based on metal oxide semiconductors (MOS) for selective gas sensors is challenging for the tasks of air quality monitoring, early fire detection, gas leaks search, breath analysis, etc. An extensive range of sensor materials has been elaborated, but no consistent guidelines can be found for choosing a material composition targeting the selective detection of specific gases. Fundamental relations between material composition and sensing behavior have not been unambiguously established. In the present review, we summarize our recent works on the research of active sites and gas sensing behavior of n-type semiconductor metal oxides with different composition (simple oxides ZnO, In2O3, SnO2, WO3; mixed-metal oxides BaSnO3, Bi2WO6), and functionalized by catalytic noble metals (Ru, Pd, Au). The materials were variously characterized. The composition, metal-oxygen bonding, microstructure, active sites, sensing behavior, and interaction routes with gases (CO, NH3, SO2, VOC, NO2) were examined. The key role of active sites in determining the selectivity of sensor materials is substantiated. It was shown that the metal-oxygen bond energy of the MOS correlates with the surface acidity and the concentration of surface oxygen species and oxygen vacancies, which control the adsorption and redox conversion of analyte gas molecules. The effects of cations in mixed-metal oxides on the sensitivity and selectivity of BaSnO3 and Bi2WO6 to SO2 and VOCs, respectively, are rationalized. The determining role of catalytic noble metals in oxidation of reducing analyte gases and the impact of acid sites of MOS to gas adsorption are demonstrated.

Quantum Diffusion of H(D) In Semiconductors and Metals, and The Role of the Interaction with Impurities

1998 ◽  
Vol 513 ◽  
Author(s):  
G. Cannelli ◽  
R. Cantelli ◽  
F. Cordero ◽  
E. Giovine ◽  
F. Trequattrini
Keyword(s):  
Low Temperature ◽  
Energy Levels ◽  
Relaxation Rates ◽  
Doped Semiconductors ◽  
Higher Symmetry ◽  
Boron Doped ◽  
Wide Range ◽  
Diffusion Studies ◽  
Tunnel System

ABSTRACTThe mobility of hydrogen and its isotopes in metals has been the object of investigation for several years, whereas the diffusion studies of H in doped semiconductors started more recently. Although the H diffusion coefficient in metals may be several orders of magnitudes higher than in semiconductors, the dynamics of H in metals and semiconductors presents many common features, like precipitation, trapping by heavier impurities and, as indicated by recent results, quantum tunneling at low temperature.In boron doped silicon, the relaxation rates τ−1(T) of H around B obtained from anelastic relaxation were joined with those from infrared absorption: the remarkably wide range obtained (11 decades) clearly shows a deviation of τ−1(T) from the classical dependence at low temperature. However, the results obtained and their analysis do not allow yet to draw conclusions on the mechanism governing the H(D) dynamics.Recently, the investigation of the dynamics of H(D) in GaAs doped with Zn revealed a dissipation peak at 20 K in the kHz range. This relaxation has the highest rate found for H in a semiconductor: more than 15 orders of magnitude higher than in all the other semiconductors measured so far. The analysis of the dissipation curves clearly indicates that the nature of the H reorientation is quantistic.In metals two regimes of the H mobility are observed: hopping with deviations from a classical Arrhenius motion, and a much faster tunneling within few close sites. In the latter regime the H dynamics does not consist of jumps but of transitions between the quantized energy levels of the tunnel systems. The types of interactions assisting the H transitions and the geometry of the tunnel systems are an open problem: although the two-level tunnel system (TLS) has been widely used to explain neutron diffusion, specific heat, and acoustic spectroscopy results in interstitial solutions (NbOxHy), recently this model has appeared not to be valid in substitutional solutions (NbZrxHy, NbTixHy) where the tunnel systems have a higher symmetry. The four-level systems seem to be more appropriate, although the corresponding model has not been developed as much as the TLS yet.

Investigation of an Ionic Liquid As a High-Temperature Electrolyte for Silicon-Lithium Systems

2020 ◽  
Author(s):  
Christopher Rudolf ◽  
Corey Love ◽  
Marriner Merrill
Keyword(s):  
Ionic Liquid ◽  
Ionic Liquids ◽  
Solid State ◽  
High Temperatures ◽  
Room Temperature ◽  
Elevated Temperatures ◽  
Lithium Ion ◽  
Constant Current ◽  
Wide Range ◽  
Solid State Electrolytes

Abstract Electrolytes for lithium ion batteries which work over a wide range of temperatures are of interest in both research and applications. Unfortunately, most traditional electrolytes are unstable at high temperatures. As an alternative, solid state electrolytes are sometimes used. These are inherently safer because they have no flammable vapors, and solid state electrolytes can operate at high temperatures, but they typically suffer from very low conductivity at room temperatures. Therefore, they have had limited use. Another option which has been previously explored is the use of ionic liquids. Ionic liquids are liquid salts, with nominally zero vapor pressure. Many are liquid over the temperature of interest (20–200°C). And, there is a tremendous range of available chemistries that can be incorporated into ionic liquids. So, ionic liquids with chemistries that are compatible with lithium ion systems have been developed and demonstrated experimentally at room temperature. In this study, we examined a silicon-lithium battery cycling at room temperature and over 150°C. Using half-cell vial and split-cell structures, we examined a standard electrolyte (LiPF6) at room temperature, and an ionic liquid electrolyte (1-ethyl-3-methylimidazolium bis(trifluorosulfonyl)imide) at room temperature and up to ∼150°C. The ionic liquid used was a nominally high purity product purchased from Sigma Aldrich. It was selected based on results reported in the open literature. The anode used was a wafer of silicon, and the cathode used was an alumina-coated lithium chip. The cells were cycled either 1 or 5 times (charge/discharge) in an argon environment at constant current of 50 μA between 1.5 and 0.05 volts. The results for the study showed that at room temperature, we could successfully cycle with both the standard electrolyte and the lithium ion electrolyte. As expected, there was large-scale fracture of the silicon wafer with the extent of cracking having some correlation with first cycle time. We were unable to identify any electrolyte-specific change in the electrochemical behavior between the standard electrolyte and the ionic liquid at room temperature. Although the ionic liquid was successfully used at room temperature, when the temperature was increased, it behaved very differently and no cells were able to successfully cycle. Video observations during cycling (∼1 day) showed that flocs or debris were forming in the ionic liquid and collecting on the electrode surface. The ionic liquid also discolored during the test. Various mechanisms were considered for this behavior, and preliminary tests will be presented. All materials were stable at room temperature, and the degradation appeared to be linked to the electrochemical process. As a conclusion, our working hypothesis is that, particularly at elevated temperatures, ionic liquid cleanliness and purity can be far more important than at room temperature, and small impurities can cause significant hurdles. This creates an important barrier to research efforts, because the “same” ionic liquids could cause failure in one situation and not in another due to impurities.

Role of Combustion Chemistry in Low-Temperature Deposition of Metal Oxide Thin Films from Solution

2017 ◽  
Vol 29 (21) ◽  
pp. 9480-9488 ◽  
Author(s):  
Elizabeth A. Cochran ◽  
Deok-Hie Park ◽  
Matthew G. Kast ◽  
Lisa J. Enman ◽  
Cory K. Perkins ◽  
...  
Keyword(s):  
Thin Films ◽  
Low Temperature ◽  
Metal Oxide ◽  
Oxide Thin Films ◽  
Combustion Chemistry ◽  
Metal Oxide Thin Films ◽  
Low Temperature Deposition ◽  
Temperature Deposition
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