Drop In Conductivity Research Articles

Controls of low injectivity caused by interaction of reservoir and clogging processes in a sedimentary geothermal aquifer (Mezőberény, Hungary)

Low injectivity is often experienced in geothermal doublets installed in sandstone reservoirs. This even led to a shutdown of the Mezőberény (Hungary) geothermal site. An on-site campaign was carried out in January 2021 to prepare a stimulation aiming to enhance the transmissivity of the sedimentary reservoir and the near-wellbore zone of this site. Previous studies have concluded that insufficient injectivity may be linked to a high skin effect in the near well-bore zone and pore clogging in combination with the low net sandstone content of the fluvio-deltaic reservoir. A chemical soft stimulation based on the injection of hydrochloric acid (HCl) was successfully used to unclog and recover the well injectivity. Despite such empirical evidence, the geochemical mechanisms leading to both, detrimental formation of clogging and the HCl-driven transmissivity restoration, have not yet been elucidated. This work presents the results of a novel analysis aiming at (a) predicting the dominant type of clogging forming in the near-well bore zone; (b) quantifying the drop in hydraulic conductivity as clogging occurs; and (c) supporting the optimization of the HCl dosage during the chemical soft stimulation. The study is supported by new experimental datasets never presented before from the Mezőberény site and a geochemical model set-up simulating the main mechanisms involved in the clogging and unclogging processes. It is concluded that the biofilm formation was the dominant, while the precipitation of calcite and amorphous ferrihydrite—later reduced to magnetite by microbes—was the secondary clogging mechanism: In the long-term (yearly scale) simulating the hydraulic conductivity showed a decline with forming scales; therefore, biofilm was presumably responsible for the experienced rapid (1 month) clogging. When modelling the chemical stimulation, the estimated amount of precipitated minerals was dissolved already with 2.5 mol of HCl per liter of water (~ 10 m/m%). Therefore, the 20 m/m% of HCl chosen during the field campaign might had a beneficial effect dissolving the potentially higher amount of scaling and/or the carbonate minerals of the matrix near the wellbore. Overall, it is concluded that the chemical and the microbial analyses together with the geochemical model were critical to tailor the remediation attempts and to propose further development or reconstruction of the surface system before going into operation to prevent recurrent impairments. Our findings highlight the importance of interactions of various clogging mechanisms with each other as well as with the reservoir processes and provide approaches to tackle the issue of injectivity drop by characterizing and quantifying their effects.

Role of Sintering Aids in Electrical and Material Properties of Yttrium- and Cerium-Doped Barium Zirconate Electrolytes

Ceramic proton conductors have the potential to lower the operating temperature of solid oxide cells (SOCs) to the intermediate temperature range of 400–600 °C. This is attributed to their superior ionic conductivity compared to oxide ion conductors under these conditions. However, prominent proton-conducting materials, such as yttrium-doped barium cerates and zirconates with specified compositions like BaCe1−xYxO3−δ (BCY), BaZr1−xYxO3−δ (BZY), and Ba(Ce,Zr)1−yYyO3−δ (BCZY), face significant challenges in achieving dense electrolyte membranes. It is suggested that the incorporation of transition and alkali metal oxides as sintering additives can induce liquid phase sintering (LPS), offering an efficient method to facilitate the densification of these proton-conducting ceramics. However, current research underscores that incorporating these sintering additives may lead to adverse secondary effects on the ionic transport properties of these materials since the concentration and mobility of protonic defects in a perovskite are highly sensitive to symmetry change. Such a drop in ionic conductivity, specifically proton transference, can adversely affect the overall performance of cells. The extent of variation in the proton conductivity of the perovskite BCZY depends on the type and concentration of the sintering aid, the nature of the sintering aid precursors used, the incorporation technique, and the sintering profile. This review provides a synopsis of various potential sintering techniques, explores the influence of diverse sintering additives, and evaluates their effects on the densification, ionic transport, and electrochemical properties of BCZY. We also report the performance of most of these combinations in an actual test environment (fuel cell or electrolysis mode) and comparison with BCZY.

Chemistry of Reduced Graphene Oxide: Implications for the Electrophysical Properties of Segregated Graphene-Polymer Composites.

Conductive polymer composites (CPCs) with nanocarbon fillers are at the high end of modern materials science, advancing current electronic applications. Herein, we establish the interplay between the chemistry and electrophysical properties of reduced graphene oxide (rGO), separately and as a filler for CPCs with the segregated structure conferred by the chemical composition of the initial graphene oxide (GO). A set of experimental methods, namely X-ray photoelectron spectroscopy (XPS), ultraviolet-visible spectroscopy, van der Paw and temperature-dependent sheet resistance measurements, along with dielectric spectroscopy, are employed to thoroughly examine the derived materials. The alterations in the composition of oxygen groups along with their beneficial effect on nitrogen doping upon GO reduction by hydrazine are tracked with the help of XPS. The slight defectiveness of the graphene network is found to boost the conductivity of the material due to facilitating the impact of the nitrogen lone-pair electrons in charge transport. In turn, a sharp drop in material conductivity is indicated upon further disruption of the π-conjugated network, predominantly governing the charge transport. Particularly, the transition from the Mott variable hopping transport mechanism to the Efros-Shklovsky one is signified. Finally, the impact of rGO chemistry and physics on the electrophysical properties of CPCs with the segregated structure is evaluated. Taken together, our results give a hint at how GO chemistry manifests the properties of rGO and the CPC derived from it, offering compelling opportunities for their practical applications.

Thermoelectric properties of A-site deficient reduced Sr0.775La0.15-xEuxTiO3-δ (0 ≤ x ≤ 0.15)

There are numerous different schemes to improve the figure of merit (ZT) in oxide thermoelectrics, including creating additional electrons using oxygen vacancies, chemical doping, and A-site nonstoichiometry. A-site deficient (Sr,La)0.925TiO3- δ has shown promise as an n-type oxide thermoelectric; herein, additional A-site substitutional doping with Eu was used to improve ZT, through a combination of A-site size mismatch and non-stoichiometry. A solid solution series Sr0.775La0.15-xEuxTiO3-δ (0 ≤ x ≤ 0.15) was synthesised, showing a modest improvement in thermoelectric properties for x = 0.05, with a ZT of 0.18 at 600 °C, vs a ZT of 0.16 in the end member composition. Upon full characterisation, the additional electrons provided by the formation of oxygen vacancies were being used up by reduction of the added europium dopants, leading to a drop in electrical conductivity, and correspondingly, ZT. This gives a useful perspective in choosing dopants for schemes such as these.

Characterising the discharge of hillslope karstic aquifers from hydrodynamic and physicochemical data (Sierra Seca, SE Spain)

Groundwater flow has been investigated in the Sierra Seca, Spain. Maximum recharge to the central core of the mountain occurs at high elevations, which provides recharge to two overlapping karst aquifers constituting a groundwater storage zone at a lower elevation break in slope. Both karst aquifers are associated with three springs arising from the upper part of the permeable formations. The climate is characterized by long and intense periods of drought and short periods of rainfall, which trigger discharges from the springs. Spring flow recession curve analysis, cross-correlation and monitoring of groundwater temperature and electrical conductivity have demonstrated contrasts observed in the hydrodynamic and physicochemical response of the three springs during flood events. One spring records floods with narrow and short peaks of high discharge accompanied by sharp drops in temperature and electrical conductivity. Another spring records floods with somewhat wider peaks and sharp increases in temperature and electrical conductivity (piston effect), whereas the third spring shows great consistency in all monitored characteristics. It is concluded that the absence of a piston effect in the spring with the highest flow rates is due to the contribution of rapidly circulating water that is expelled by semi-active karst networks (overflow) before reaching the saturated zone, which does not occur in the other springs due to the absence of overflow hydrological pathways. The most regular spring owes its functioning to the contribution of infiltrated water in the bed of an upstream riverbed, which explains this regularity.

Co-application of biochars and Piriformospora indica improved the quality of coastal saline soil and promoted the growth of forage.

Soil quality is defined as the ability of soil to maintain the soil environment and the biosphere. Due to the limitation of salt and alkali stress, soil quality can be reduced, which in turn affects agricultural production. Biochar is widely used in saline-alkali land improvement because of its special pore structure and strong ion exchange ability, while Piriformospora indica is widely used in saline-alkali land improvement because it can symbiose with plants and improve plant stress resistance. However, the synergistic effect of combined biochar application and inoculation of P. indica on the quality of saline-alkali soil and plant development is uncertain. Hence, we investigated the combined influences of biochar and P. indica on the soil physicochemical characteristics, as well as the growth and chlorophyll florescence of sorghum-sudangrass hybrids (Sorghum bicolor × Sorghum sudane) in our study. The results indicated that after applying biochar and P. indica together, there was a considerable drop in soil pH, conductivity, Na+, and Cl- concentrations. Meanwhile, the soil organic matter (SOM), available phosphorus (AP), and alkaline hydrolyzable nitrogen (AN) increased by 151.81%, 50.84%, and 103.50%, respectively, when the Bamboo biochar was combined with 120 ml/pot of P. indica. Eventually, sorghum-sudangrass hybrid biomass, transpiration rate, and chlorophyll content increased by 111.69%, 204.98%, and 118.54%, respectively. According to our findings, using P. indica and biochar together can enhance soil quality and plant growth. The results also provide insights to enhance the quality of saline-alkali soils and the role of microorganisms in nutrient cycling.

Native Defects Hybridization and Electronic Transport in Cu2Se‐CuGaSe2 Hierarchical Composites

AbstractEngineering the energy distribution of electronic defects in semiconductors can afford the coexistence of degenerate and nondegenerate transport behavior. By leveraging native defects in Cu2Se and CuGaSe2 phases, the tunability of the concentration and energy distribution of active electronic defects in hierarchical (1‐x)Cu2Se‐(x)CuGaSe2 composites is demonstrated. This study found that the electrical conductivity of various composites decreases with rising temperature indicating degenerate semiconducting behavior, whereas the carrier density increases with temperature, which is consistent with non‐degenerate semiconductivity. Remarkably, this study found that while the carrier density and electrical conductivity drop with the increasing CuGaSe2 content for samples with x ≤ 0.45 is consistent with an increase in the activation energy of “active” electronic defects, the sudden increase by 140% in the electrical conductivity and by 109% in the carrier density for near equimolar composition suggests the formation of a large density of electronic defects with lower activation energy. This unusual behavior is understood within the context of the hybridization of coexisting native electronic defects to form degenerate hybrid acceptor states with lower activation energy. The reported unique electronic transport can be leveraged for the development of more versatile electronic and optoelectronic devices with superior performance.

Thermal conductivity loss in WC-Co hard metal due to high-temperature cyclic loading damage as a function of microstructure and temperature

Many structures made of WC-Co hard metal are subject to thermo-mechanical loading and have to conduct heat in order to function properly in industrial application. The current work provides results on a significant drop in thermal conductivity of WC-Co hard metals as a function of material volume damage that accumulates during cyclic high-temperature loading of the materials depending on material microstructure. Average WC grain size and Co binder metal content of the investigated grades ranged from submicron to medium and from 10 to 12 wt%, respectively. The hard metals were subjected to uniaxial cyclic loading in a vacuum for different numbers of load cycles at 700 °C and 800 °C. Damage features accumulated in the material volume were documented by means of scanning electron microscopy. Thermal conductivity properties of virgin and damaged materials were determined via laser flash analysis. The results indicated a significant decrease depending on the materials' microstructure, i.e. the defects' predominant location within the microstructure. The damage features that occurred mainly between WC grains in the coarser-grained grade led to larger drops in thermal conductivity with rising temperature compared to damage features that occurred within the Co binder metal in the finer-grained grade. The presented results are of high relevance to the thermo-mechanical load situation of e.g. milling tools since the heat conduction away from their cutting edges is hindered by the documented effect and deemed to lead to a self-acceleration of the damage accumulation.

Elucidating the role of Ag+, Cu2+, and Fe3+ in tuning the electrical characteristics of polyaniline prepared through post-doping method

Abstract Conducting polymers possess inherent electrical conductivity, attracting significant attention in engineering applications, including dye-sensitized solar cells, gas sensors, and energy storage electrodes. Of various conducting polymers, Polyaniline has gained much attention due to its low cost of monomer, ease of bulk synthesis, high flexibility, and good environmental stability. Nevertheless, the conductivity of polyaniline is rather low when it is prepared under an un-doped state. Despite that, there is no clear information regarding how the valency of a metal dopant and its concentration can affect the electrical characteristics and other physicochemical properties of doped polyaniline. This study aims to fill this research gap by elucidating the changes in the electrical characteristics of polyaniline through metal doping. Polyaniline was synthesized through chemical oxidative polymerization in an HCl medium, followed by a post-doping to produce metal-codoped polyaniline. Three dopant materials, namely AgNO3, Cu(NO3)2, and Fe(NO3)3, were used in this synthesis, representing mono-, di-, and tri-valent metal ions, respectively. Results showed that bare PANI (which was doped with HCl only) exhibited a higher electrical conductance value of 8.44 x 10-7 S, while 1 M of Ag-codoped polyaniline, 1 M of Cu-codoped polyaniline, and 1 M of Fe-codoped polyaniline exhibited electrical conductance values of 1.73 x 10-7 S, 4.27 x 10-8 S, and 2.33 x 10-6 S, respectively. Apparently, the trivalent metal dopant was able to improve the conductivity of polyaniline; however, a detrimental effect resulted when the concentration of Fe3+ was increased to 1.5 M (overdose), resulting in a drop in electrical conductance to 4.66 x 10-8 S. In terms of morphological property, Ag-doped polyaniline exhibited a mixture of plate-like and globule-like structures, while both Cu-doped polyaniline and Fe-doped polyaniline predominantly displayed tiny globule-like structures, likely attributed to the stronger acidity of the Cu(NO3)2 and Fe(NO3)3 solutions. Meanwhile, the presence of several common bands of polyaniline such as N-H, C=N, C-H aromatic, quinoid and benzoid units are detected in the produced samples. The project outcomes are expected to guide tailored development of metal-doped polyaniline for specific electrical applications.

Sodium iodide dopant mediated enhancements in energy storage characteristics of polysaccharide polymer electrolytes

Sodium iodide dopant influencing the properties of polysaccharide polymer sodium carboxymethyl cellulose is analyzed in this work by FTIR, XRD, DSC, TGA, SEM, UTM, and electrical. Solvation of I− and Na+ ions by the −OH group has disrupted the intra– and intermolecular hydrogen bonds between the polymers escorting to a decrease in crystallinity and creating a pathway for ion diffusion. The formation of transient crosslink and the physical environment created by the polymer-ion interaction have affected the rigidity of the polymer chains as well as the thermal stability of the NaCMC−NaI system. I− ion influences the ESW of the NaCMC−NaI system by forming various iodine species. Trapping of the I− ion for the NaCMC70−NaI30 sample has resulted in a drop in ionic conductivity manifested in the transient ionic current curve. A cation transference number of 0.14 indicates the dominance of anion in the ion conduction mechanism. An energy density of 720 mWhkg−1 and power density of 60 mWkg−1 was achieved for a dry cell incorporated with a CI25 sample as the electrolyte and separator.

Unveiling zirconium phytate-heteropolyacids-ionic liquids membranes for PEM fuel cells applications up to 150 °C

In the context of escalating energy demands and the pressing issues of climate change, fuel cells emerge as a pivotal, economically feasible, and environmentally sound renewable energy alternative. This study highlights the importance of fuel cells, specifically focusing on high-temperature and Nafion-free membranes. Membranes composed of zirconium phytate, silicotungstic acid, polyethylene glycol, and ionic liquids employing porous polytetrafluoroethylene polymer for support are reported. Investigating varying ratios of silicotungstic acid, polyethylene glycol, and ionic liquids, electrochemical spectroscopy revealed heightened proton conductivity upon ionic liquids integration. Initially, the unmodified zirconium phytate membrane demonstrated a conductivity of 6.65 × 10−4 S/cm, escalating tenfold (2.23 × 10−3 S/cm) with silicotungstic acid addition. Further enhancements, such as incorporating polyethylene glycol, led to an increase in the conductivity to 3.81 × 10−2 S/cm. The maximum conductivity value obtained in this work (0.1 S/cm), comparable to Nafion, was achieved with 5.86 wt% of the 1-Hexyl-3-methylimidazolium tricyanomethanide. Testing at elevated temperatures up to 150 °C revealed a drop in conductivity by two orders of magnitude (10−3 S/cm), highlighting their remarkable conductive properties. Additionally, water uptake analysis demonstrated the membranes' ability to retain more than 60 wt% water molecules within their matrix. Furthermore, thermogravimetric analysis revealed the thermal stability of membranes at high temperatures up to 600 °C. These findings strongly indicate that these synthesized membranes possess considerable potential for high temperature proton exchange membrane fuel cell applications.

Electrical conductivity of siderite and the effect of the spin transition of iron

We have conducted electrical conductivity measurements of FeCO3 siderite under high pressure up to 63 GPa in order to understand the nature and effect of iron spin transition and its influence on the geophysical properties of siderite, which is an end-member of major carbonate minerals. The results from Raman and Mössbauer spectroscopic measurements show that the high- to low-spin transition of iron occurs at around 50 GPa in agreement with previous studies. A sharp decrease of the electrical conductivity was also observed at around 50 GP, which is associated with the spin transition in iron. Although the stability of FeCO3 siderite may be limited under high-temperature conditions along with the mantle geotherm, solid solutions in the MgCO3-FeCO3 system, Mg1-xFexCO3, could be stable up to the pressure-temperature condition of the lowermost mantle. The pressure-temperature range of the spin transition in Mg1-xFexCO3 is narrower than those of the major lower mantle minerals, ferropericlase and bridgmanite, and thus the drop of the electrical conductivity induced by the spin transition could be clearer under lower mantle conditions. Therefore, the existence of Mg1-xFexCO3 may affect the observed heterogeneity of electrical conductivity in the mid-lower mantle.

Electron irradiation effects on the optical properties of Hf- and Zn-doped β-Ga2O3

Optical and electrical properties of Hf- and Zn-doped β-Ga2O3 samples, which are n-type and insulating, respectively, were altered via high-energy electron irradiation at 2.5 or 0.5 MeV. The β-Ga2O3:Hf samples irradiated with 2.5 MeV electrons experienced a color change from blue to yellow and a large drop in conductivity, attributed to the creation of gallium vacancies, which compensate donors. This irradiation resulted in the absence of free carrier absorption and the presence of Cr3+ photoluminescence (PL). PL mapping prior to irradiation revealed optically active ZnO precipitates that formed during the growth of β-Ga2O3:Zn. These precipitates have a 384 nm (3.23 eV) stacking fault emission in the core; in the outer shell of the precipitate, the PL blue-shifts to 377 nm (3.29 eV) and a broad defect band is observed. After 0.5 MeV electron irradiation, the defect band broadened and increased in intensity. The blue PL band (435 nm) of β-Ga2O3 was enhanced for both Hf- and Zn-doped samples irradiated with 0.5 MeV. This enhancement is correlated with an increase in oxygen vacancies.

The effect of amorphous silica on soil–plant–water relations in soils with contrasting textures

This study investigates how amorphous silica (ASi) influences soil–plant–water interactions in distinct soil textures. A sandy loam and silty clay soil were mixed with 0 and 2% ASi, and their impact on soil retention and soil hydraulic conductivity curves were determined. In parallel, tomato plants (Solanum lycopersicum L.) were grown in experimental pots under controlled conditions. When plants were established, the soil was saturated, and a controlled drying cycle ensued until plants reached their wilting points. Soil water content, soil water potential, plant transpiration rate, and leaf water potential were monitored during this process. Results indicate a positive impact of ASi on the sandy loam soil, enhancing soil water content at field capacity (FC, factor of 1.3 times) and at permanent wilting point (PWP, a factor of 3.5 times), while its effect in silty clay loam was negligible (< 1.05 times). In addition, the presence of ASi prevented a significant drop in soil hydraulic conductivity (Kh\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${K}_{h}$$\\end{document}) at dry conditions. The Kh\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${K}_{h}$$\\end{document} of ASi-treated sandy loam and silty clay at PWP were 4.3 times higher than their respective control. Transpiration rates in plants grown in ASi-treated sandy loam soil under soil drying conditions were higher than in the control, attributed to improved soil hydraulic conductivity. At the same time, no significant difference was observed in the transpiration of plants treated with ASi in silty clay soil. This suggests ASi boosts soil–plant–water relationships in coarse-textured soils by maintaining heightened hydraulic conductivity, with no significant effect on fine-textured soils.

Sulfur-containing soft Lewis base polymers for improved lithium-ion conductivity under polymer-in-salt conditions

Abstract Solid polymer electrolytes have been intensively studied to improve the safety and energy density of lithium-ion batteries (LiBs). Although high-rate performance of LiBs has been reported in electrolytes under polymer-in-salt conditions with an excess of lithium salts and polymers, effective conditions for achieving high ionic conductivity remain unresolved. In this study, we elucidate the mechanism and high Li-ion transportability of poly(sulfone-thioether) under polymer-in-salt conditions. In particular, the composition of the polymer with an asymmetric Li salt, lithium(fluorosulfonyl)(trifluoromethane sulfonyl)imide (LiFTFSI), induced a high ionic conductivity above 10−5 S/cm, which is higher than that of the poly(ethylene oxide) (PEO)-Li salt system. Under polymer-in-salt conditions, the enhanced conductivity of poly(sulfone-thioether) contrasts with the conductivity drop observed in the conventional PEO system. These results show the superiority of polymers with soft Lewis bases, such as sulfur donor atoms, for Li-ion transport under polymer-in-salt conditions.

Physico-electrical properties of starch-based bioplastic enhanced with acid-treated cellulose and graphene oxide fillers

Biopolymer composites represent an emerging alternative to petroleum-derived polymers for applications in electronic devices. Cellulose from Luffa cylindrical was treated with acid, and graphene oxide was produced from waste battery rod graphite. The two products were characterized using FTIR, SEM, TGA and XRD. After that, starch-based bioplastic films with varying amounts of acid-treated cellulose (ALC-cellulose) and graphene oxide (GO) as fillers were prepared, and the physical and electrical properties were determined. XRD data revealed a crystallinity of 62% for the ALC-cellulose and 52% for the cellulose precursor. GO had a d-spacing of 0.76 nm compared to 0.29 nm for battery-sourced graphite. TEM micrograph analyses revealed an average fibre diameter of 44.7 nm for acid-treated cellulose and 99.7 nm for cellulose. The density, thickness, opacity, and tensile strength of the bioplastic films increased from 1.31 to 1.44 g/cm3, 0.21–0.48 mm, 14.78–38.64, and 0.98–1.42 MPa, respectively, while the moisture content, swelling ability, and porosity reduced, with an increase in percentage composition of the filler materials. The dielectric constant and conductivity increased from 50.3 to 6965.2 and 0.0036–0.0147 S/m with an increase in percentage composition of the filler materials except for Filmcr4, which showed a drop in dielectric constant (3033.73) and conductivity (0.0074 S/m). Overall, this study has demonstrated that bioplastic filler materials can be sourced from waste materials and that these fillers improved the starch-based bioplastic film's physical and electrical properties.

Statistical Mechanics of Electrowetting.

We derive the ab initio equilibrium statistical mechanics of the gas-liquid-solid contact angle on planar periodic, monodisperse, textured surfaces subject to electrowetting. To that end, we extend an earlier theory that predicts the advance or recession of the contact line amount to distinct first-order phase transitions of the filling state in the ensemble of nearby surface cavities. Upon calculating the individual capacitance of a cavity subject to the influence of its near neighbors, we show how hysteresis, which is manifested by different advancing and receding contact angles, is affected by electrowetting. The analysis reveals nine distinct regimes characterizing contact angle behavior, three of which arise only when a voltage is applied to the conductive liquid drop. As the square voltage is progressively increased, the theory elucidates how the drop occasionally undergoes regime transitions triggering jumps in the contact angle, possibly changing its hysteresis, or saturating it at a value weakly dependent on further voltage growth. To illustrate these phenomena and validate the theory, we confront its predictions with four data sets. A benefit of the theory is that it forsakes trial and error when designing textured surfaces with specific contact angle behavior.

Contrasting Regulation of Phaseolus vulgaris Root Hydraulic Properties Under Drought and Saline Conditions by Three Arbuscular Mycorrhizal Fungal Species From Soils with Divergent Moisture Regime

PurposeArbuscular mycorrhizal fungi (AMF) may help plants to overcome abiotic stresses, in part by improving their water uptake capacity. However how different AMF isolated from different climatic regions regulate plant abiotic stress tolerance and water uptake capacity is barely studied. The aim of this study was to reveal how three AMF isolated from two Mediterranean climate locations contrasting in annual precipitation, modify bean (Phaseolus vulgaris L.) root hydraulic properties facing drought and salinity.MethodsRhizophagus intraradices (Ri) and Funneliformis mosseae (Fm) were isolated from a humid area, whereas Claroideoglomus etunicatum (Ce) was isolated from a dry location. All plants (inoculated or not) were subjected to four days of withholding water or salt treatment. Root hydraulic properties including root hydraulic conductivity and aquaporin expression and abundance were determined.ResultsAll three AMF isolate induced significant differences in plant physiology regardless their different mycorrhizal colonization extent. Drought treatment diminished root hydraulic conductivity and only Fm inoculated plants featured measurable amount of sap exudate. After salt irrigation, AMF inoculation counterbalanced the drop of root hydraulic conductivity. In such situation two AMF, Fm and Ce, presented lowered phosphorylated (Ser-283) PIP2 AQP amount. AQP gene expression highlighted the importance of PvPIP1;2 and PvPIP2;3 plasticity in plants facing osmotic stress. After drought treatment AMF species from the humid location, Ri and Fm, improved plant water status and Fm enhanced root hydraulic conductivity, whereas all AMF performed similarly after salt irrigation, enhancing stomatal conductance and root hydraulic conductivity.ConclusionUnder drought conditions, the AMF isolates from humid regions were the ones that most effectively improved plant water relations. However, under salt stress, all three AMF isolates exhibited similar behavior. Therefore, to some extent, the climatic origin of the AMF could have influenced the response of host plants to drought stress, suggesting that those originating from dry areas may not necessarily be the most efficient.

Structural, thermal, surface, and electrical properties of Bi2O3 ceramics co–doped with Er–Ho–Tb rare earths

Face–centered cubic–Bi2O3 (δ–phase) material is a better ion conductor when compared to other types of solid electrolytes that have been declared in the literature due to its anion–defective crystal configuration, and hence it can be a promising solid electrolyte choice for intermediate temperature SOFC applications. In this research, Er–Ho–Tb co–doped Bi2O3 compounds were successfully synthesized by the solid–state reaction method and characterized using the XRD, TG & DTA, FPPT, and FE–SEM techniques. Apart from sample 4Er4Ho4Tb, each sample became stable with a cubic δ–phase at room temperature, according to XRD patterns. The DTA curves revealed no exothermic or endothermic peaks, implying a phase change in the constant heating cycle. The conductivity of Ho–rich compositions was higher than that of others, confirming the impact of cation polarizability on conductivity. In addition, at 700 °C, the sample 4Er8Ho4Tb with 1:2:1 content ratios had the highest conductivity of 0.29 S/cm. The porosity on the grain boundaries increased with doping, leading to higher grain boundary resistance, which could be responsible for the conductivity drop.

High-Performance PEEK/MWCNT Nanocomposites: Combining Enhanced Electrical Conductivity and Nanotube Dispersion.

High-performance engineering thermoplastics offer lightweight and excellent mechanical performance in a wide temperature range. Their composites with carbon nanotubes are expected to enhance mechanical performance, while providing thermal and electrical conductivity. These are interesting attributes that may endow additional functionalities to the nanocomposites. The present work investigates the optimal conditions to prepare polyether ether ketone (PEEK)/multi-walled carbon nanotube (MWCNT) nanocomposites, minimizing the MWCNT agglomerate size while maximizing the nanocomposite electrical conductivity. The aim is to achieve PEEK/MWCNT nanocomposites that are suitable for melt-spinning of electrically conductive multifilament's. Nanocomposites were prepared with compositions ranging from 0.5 to 7 wt.% MWCNT, showing an electrical percolation threshold between 1 and 2 wt.% MWCNT (107-102 S/cm) and a rheological percolation in the same range (1 to 2 wt.% MWCNT), confirming the formation of an MWCNT network in the nanocomposite. Considering the large drop in electrical conductivity typically observed during melt-spinning and the drawing of filaments, the composition PEEK/5 wt.% MWCNT was selected for further investigation. The effect of the melt extrusion parameters, namely screw speed, temperature, and throughput, was studied by evaluating the morphology of MWCNT agglomerates, the nanocomposite rheology, and electrical properties. It was observed that the combination of the higher values of screw speed and temperature profile leads to the smaller number of MWCNT agglomerates with smaller size, albeit at a slightly lower electrical conductivity. Generally, all processing conditions tested yielded nanocomposites with electrical conductivity in the range of 0.50-0.85 S/cm. The nanocomposite processed at higher temperature and screw speed presented the lowest value of elastic modulus, perhaps owing to higher matrix degradation and lower connectivity between the agglomerates. From all the process parameters studied, the screw speed was identified to have the higher impact on nanocomposite properties.