TUNGSTEN OXIDES AND BRONZES: SYNTHESIS, DIFFUSION AND REACTIVITY

1993 ◽  
Vol 07 (23n24) ◽  
pp. 4145-4164 ◽  
Author(s):  
JING-DONG GUO ◽  
M. STANLEY WHITTINGHAM

The tungsten oxides and bronzes have been extensively studied since their discovery in the last century, because of their brilliant colors and high electrical conductivity. More recently the driving interest resulted from their potential use in electrochromic displays and other electrochemical systems. Their crystalline structures are generally based on the corner sharing of WO 6 octahedra giving tunnels of variable size and shape leading to exciting intercalation chemistry. These structures readily undergo redox reactions, and in the last quarter century these reactions have often involved soft chemistry. Most recently hydrothermal techniques have been used to prepare new sodium tungstates with the hexagonal tungsten bronze and the pyrochlore structures. The phase formed is a function of the pH of the reaction medium. The pyrochlore phase readily undergoes ion-exchange with a wide range of monovalent cations giving the compounds, M x W 2 O 6+x/2 · y H 2 O ; the value of y is strongly dependent on the identity of the cation, M. WO 3 with the pyrochlore structure could be formed from the hydronium and ammonium complexes. Lithium can be readily intercalated either chemically and electrochemically into both these phases, just as in the previously-known bronze phases. Surprisingly more lithium is incorporated in most cases in the hexagonal than in the pyrochlore phase. The ions in the pyrochlore structure show rapid ionic mobility, with the hydronium ion showing the greatest mobility.

2020 ◽  
Vol 75 (11) ◽  
pp. 913-919
Author(s):  
Frank Krumeich

AbstractSince the 1970s, high-resolution transmission electron microscopy (HRTEM) is well established as the most appropriate method to explore the structural complexity of niobium tungsten oxides. Today, scanning transmission electron microscopy (STEM) represents an important alternative for performing the structural characterization of such oxides. STEM images recorded with a high-angle annular dark field (HAADF) detector provide not only information about the cation positions but also about the distribution of niobium and tungsten as the intensity is directly correlated to the local scattering potential. The applicability of this method is demonstrated here for the characterization of the real structure of Nb7W10O47.5. This sample contains well-ordered domains of Nb8W9O47 and Nb4W7O31 besides little ordered areas according to HRTEM results. Structural models for Nb4W7O31 and twinning occurring in this phase have been derived from the interpretation of HAADF-STEM images. A remarkable grain boundary between well-ordered domains of Nb4W7O31 and Nb8W9O47 has been found that contains one-dimensionally periodic features. Furthermore, short-range order observed in less ordered areas could be attributed to an intimate intergrowth of small sections of different tetragonal tungsten bronze (TTB) based structures.


Molecules ◽  
2020 ◽  
Vol 25 (14) ◽  
pp. 3211
Author(s):  
Esakkiammal Sudha Esakkimuthu ◽  
Nathalie Marlin ◽  
Marie-Christine Brochier-Salon ◽  
Gérard Mortha

Lignin is an aromatic biopolymer derived from lignocellulosic biomass. Providing a comprehensive structural analysis of lignin is the primary motivation for the quantification of various functional groups, with a view to valorizing lignin in a wide range of applications. This study investigated the lignin fluorobenzylation reaction and performed a subsequent 19F-NMR analysis to quantify hydroxyl groups, based on a work developed two decades ago by Barrelle et al. The objectives were to check the assignments proposed in this previous study and to examine the reactivity of various types of lignin hydroxyls with the derivatization agent. Selected lignin model compounds containing phenolic and aliphatic hydroxyls were subjected to the fluorobenzylation reaction, and the obtained reaction medium was analyzed by 13C and 19F NMR spectroscopy. The model compound results showed that phenolic hydroxyls were totally derivatized, whereas aliphatic hydroxyls underwent minimal conversion. They also confirmed that 19F NMR chemical shifts from −115 ppm to −117.3 ppm corresponded to phenolic groups. Then, a 19F NMR analysis was successfully applied to Organosolv commercial lignin after fluorobenzylation in order to quantify its phenolic group content; the values were found to be in the range of the reported values using other analytical techniques after lignin acetylation.


Soil Research ◽  
2012 ◽  
Vol 50 (1) ◽  
pp. 44 ◽  
Author(s):  
M. A. Mojid ◽  
H. Cho

This study explored the effects of water content and temperature on the mobility of exchangeable cations (termed the surface ionic mobility and hereafter ionic mobility) in the hydration layers of bentonite clay. The ionic mobility directly governs the surface conductivity of the clay. The investigation was done by measuring the bulk electrical conductivity (EC) of four sand–bentonite mixtures of different proportions for a wide range of water contents under constant temperature, and three bentonite samples at different water contents over 5–90°C. The ionic mobility was determined from the surface conductivity at the mean ionic strength of the hydration layers. The ionic mobility in the sand–bentonite samples increased with an increase in hydration layer thickness. For a given thickness of the hydration layer, the greater the bentonite content of a sample, the smaller was the ionic mobility. The ionic mobility in the bentonite samples at different water contents also increased, at reduced rates, with a rise in temperature. Consequently, the surface conductivity of the samples increased non-uniformly, at two different rates, with an increase in temperature. The increasing rate of this conductivity depended on temperature; over the low temperature range which depended on the water content, the rate was 0.013 dS/m.K, and over higher temperature range, the rate decreased to 0.008 dS/m.K. The commonly used temperature correction factor, 0.019 dS/m.K, for EC therefore did not hold true for the bentonite samples.


2004 ◽  
Vol 19 (5) ◽  
pp. 1575-1580 ◽  
Author(s):  
Jie Lian ◽  
Rodney C. Ewing ◽  
L.M. Wang ◽  
K.B. Helean

Ceramics with III-IV pyrochlore compositions, A3+2B4+2O7 (A = Y and rare earth elements; B = Ti, Zr, Sn, or Hf), show a wide range of responses to ion-beam irradiation. To evaluate the role of the B-site cations on the radiation stability ofthe pyrochlore structure-type, Gd2Sn2O7 and Gd2Hf2O7 have been irradiated by1 MeV Kr+. The results are discussed in terms of the ionic size and type ofbonding of Sn4+ and Hf4+ and compared to previous results for titanate andzirconate pyrochlores. Gd2Sn2O7 is sensitive to ion beam–induced amorphizationwith a critical amorphization dose of approximately 3.4 displacements per atom(dpa) (2.62 × 1015 ions/cm2) at room temperature and a critical amorphization temperature of approximately 350 K. Gd2Hf2O7 does not become amorphous at adose of approximately 4.54 displacement per [lattice] atom (3.13 × 1015 ions/cm2) at room temperature, but instead is transformed to a disordered fluorite structure upon ion-beam irradiation. Although the radius ratio of the A- to B-site cations provides a general indication of the type of radiation response of different pyrochlore compositions, the results for Gd2Sn2O7 emphasize the importance of bond type, particularly the covalency of the 〈Sn–O〉 bond in determining the radiation response.


2003 ◽  
Vol 21 (2) ◽  
pp. 367-376 ◽  
Author(s):  
Piotr Górecki

Susan Reynolds's article is a culmination and a turning point. It builds on several approaches to medieval law and culture, of which two strike me as especially important. One is a study of legal history as a domain of human activity, especially habitual or routine activity, pursued by a wide range of social groups. The other is a search for the meaning and the criteria of the enormous transition during the central Middle Ages, which Christopher Dawson at the dawn of this subject, and Robert Bartlett in its currently definitive moment, have identified as “the making of Europe.” The first subject exists above all thanks to the work of Reynolds herself, while the second is an outcome of a number of quite distinct scholarly trajectories, spanning several generations. Apart from some suggestive and implicit links, those two subjects have, over the past quarter century, been pursued separately. Reynolds's article brings them together.


Open Physics ◽  
2008 ◽  
Vol 6 (4) ◽  
Author(s):  
Priyadarshini Sahoo ◽  
Anuradha Panigrahi ◽  
Sunanda Patri ◽  
Ram Choudhary

AbstractPolycrystalline samples of Ba4SrRTi3V7O30 (R=Sm and Dy), members of the tungsten-bronze family, were prepared using a high-temperature, solid-state reaction technique and studied their electrical properties (using complex impedance spectroscopy) in a wide range of temperature (31–500°C) and frequency (1 kHz-1 MHz). Preliminary structural (XRD) analyses of these compounds show the formation of single-phase, orthorhombic structures at room temperature. The scanning electron micrographs (SEM) provided information on the quality of the samples and uniform distribution of grains over the entire surface of the samples. Detailed studies of the dielectric properties suggest that they have undergone ferroelectric-paraelectric phase transition well above the room temperatures (i.e., 432 and 355°C for R= Sm and Dy, respectively, at frequency 100 kHz). Measurements of electrical conductivity (ac and dc) as a function of temperature suggest that the compounds have semiconducting properties much above the room temperature, with negative temperature coefficient of resistance (NTCR) behavior. The existence of ferroelectricity in these compounds was confirmed from a polarization study.


Author(s):  
Negisa Ebadipour ◽  
Sébastien Paul ◽  
Benjamin Katryniok ◽  
Franck Dumeignil

Polyglycerols (PGs) are biocompatible and highly functional polyols with a wide range of applications, such as emulsifiers, stabilizers, antimicrobial agents, in many industries including cosmetics, food, plastic and biomedical. The demand increase for biobased PGs encourages researchers to develop new catalytic systems for glycerol polymerization. This review focuses on alkaline homogeneous and heterogeneous catalysts. The performances of the alkaline catalysts are compared in terms of conversion and selectivity, and their respective advantages and disadvantages are commented. While homogeneous catalysts exhibit a high catalytic activity, they cannot be recycled and reused, whereas solid catalysts can be partially recycled. The key issue for heterogenous catalytic systems, which is unsolved so far, is linked to their instability due to partial dissolution in the reaction medium. Further, this paper also reviews the proposed mechanisms of glycerol polymerization over alkaline-based catalysts and discuss the various operating conditions with an impact on the performances. More particularly, temperature and amount of catalyst proved to have a significant influence on glycerol conversion and on its polymerization extent.


PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e11646
Author(s):  
Liubov Igorevna Trubitsina ◽  
Azat Vadimovich Abdullatypov ◽  
Anna Petrovna Larionova ◽  
Ivan Vasilyevich Trubitsin ◽  
Sergey Valerievich Alferov ◽  
...  

Background Two-domain laccases are copper-containing oxidases found in bacteria in the beginning of 2000ths. Two-domain laccases are known for their thermal stability, wide substrate specificity and, the most important of all, their resistance to so-called «strong inhibitors» of classical fungal laccases (azides, fluorides). Low redox potential was found to be specific for all the two-domain laccases, due to which these enzymes lost the researchers’ interest as potentially applicable for various biotechnological purposes, such as bioremediation. Searching, obtaining and studying the properties of novel two-domain laccases will help to obtain an enzyme with high redox-potential allowing its practical application. Methods A gene encoding two-domain laccase was identified in Catenuloplanes japonicus genome, cloned and expressed in an Echerichia coli strain. The protein was purified to homogeneity by immobilized metal ion affinity chromatography. Its molecular properties were studied using electrophoresis in native and denaturing conditions. Physico-chemical properties, kinetic characteristics, substrate specificity and decolorization ability of laccase towards triphenylmethane dyes were measured spectrophotometrically. Results A novel two-domain recombinant laccase CjSL appeared to be a multimer with a subunit molecular mass of 37 kDa. It oxidized a wide range of phenolic substrates (ferulic acid, caffeic acid, hydroquinone, catechol, etc.) at alkaline pH, while oxidizing of non phenolic substrates (K4[Fe(CN)6], ABTS) was optimal at acidic pH. The UV-visible absorption spectrum of the purified enzyme was specific for all two-domain laccases with peak of absorption at 600 nm and shoulder at 340 nm. The pH optima of CjSL for oxidation of ABTS and 2, 6-DMP substrates were 3.6 and 9.2 respectively. The temperature optimum was 70 °C. The enzyme was most stable in neutral-alkaline conditions. CjSL retained 53% activity after pre-incubation at 90 °C for 60 min. The enzyme retained 26% activity even after 60 min of boiling. The effects of NaF, NaN3, NaCl, EDTA and 1,10-phenanthroline on enzymatic activity were investigated. Only 1,10-phenanthroline reduced laccase activity under both acidic and alkaline conditions. Laccase was able to decolorize triphenylmethane dyes and azo-dyes. ABTS and syringaldehyde were effective mediators for decolorization. The efficacy of dye decolorization depended on pH of the reaction medium.


Polymers ◽  
2019 ◽  
Vol 11 (11) ◽  
pp. 1740 ◽  
Author(s):  
Byoungyun Jeon ◽  
Taehyung Kim ◽  
Dabin Lee ◽  
Tae Joo Shin ◽  
Kyung Wha Oh ◽  
...  

We present polymer nanocomposites of tungsten bronze nanorods (TBNRs) and ethylene propylene diene monomers (EPDM). The combination of these components allows the simultaneous enhancement in the mechanical and photothermal properties of the composites at low filler contents. The as-synthesized TBNRs had lengths and diameters of 14.0 ± 2.4 nm and 2.5 ± 0.5 nm, respectively, and were capped with oleylamine, which has a chemical structure similar to EPDM, making the TBNRs compatible with the bulk EPDM matrix. The TBNRs absorb a wide range of near-infrared light because of the sub-band transitions induced by alkali metal doping. Thus, the nanocomposites of TBNRs in EPDM showed enhanced photothermal properties owing to the light absorption and subsequent heat emission by the TBNRs. Noticeably, the nanocomposite with only 3 wt% TBNRs presented significantly enhanced tensile strain at break, in comparison with those of pristine EPDM, nanocomposites with 1 and 2 wt % TBNRs, and those with tungsten bronze nanoparticles, because of the alignment of the nanorods during tensile elongation. The photothermal and mechanical properties of these nanocomposites make them promising materials for various applications such as in fibers, foams, clothes with cold weather resistance, patches or mask-like films for efficient transdermal delivery upon heat generation, and photoresponsive surfaces for droplet transport by the thermocapillary effect in microfluidic devices and microengines.


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