Metal Oxide Content Research Articles

FEATURES AND EXPERIENCE OF CONVERTING GAS-OIL BOILERS OF INDUSTRIAL CHP PLANTS TO BURNING BIOMASS AND SUB-BITUMINOUS COAL

The paper examines the features of biomass as a fuel and substantiates that for agrobiomass waste with a high content of alkali metal oxides and slag properties of ash, it is more appropriate to burn it in a dense bed in the form of pellets, which ensures a temperature at the exit from the furnace of no more than 900 °C, a low part of fly ash and low content of unburned carbon in it, and so eliminates the risk of smoldering deposits with their melting and slagging. Technical solutions are given and the experience is presented of gas and oil boilers of CHP plants of sugar factories reconstruction with their transfer to the burning of biomass and/or coal in a dense bed on a direct-flow grate with the replacement of the air heater with air-water heater, with the addition of stages of the boiling economizer to compensate for the decrease in the heat perception of the furnace screens, maintaining the overall height of the boiler and the plane of the boiler cell. The reconstruction of boilers according to the developed technical solutions is possible to perform in the interval between production seasons, its implementation on boilers BKZ-75 GMA of Radekhiv and Chortkiv sugar factories allowed to achieve acceptable technical, economic and environmental indicators and ensured payback due to the difference in commercial prices of gas and of agrobiomass pellets. It is proposed to replicate the positive experience in the creation of decentralized regulating thermal generation capacities of the country. Bibl. 30, Fig. 3, Tab. 4.

Self-protected Chlorella@Mn catalyst with excellent resistance to alkali/alkaline earth metal for NOx reduction by NH3

In the selective catalytic reduction of NOx by NH3 (NH3-SCR), conventional Mn-based denitration catalysts often suffered from susceptibility to poisoning by alkali and alkaline earth metals, this paper presented an innovative self-protected Chlorella@Mn denitration catalyst. Remarkably, in the presence of high concentrations (2 wt%) of alkali and alkaline earth metal oxides, the Chlorella@Mn catalyst sustained a NOx conversion exceeding 96 % at 175 °C. At an even higher concentration (4 wt%), NOx conversion above 90 % at 175 °C, surface analysis revealed that POMn sites acted as sacrificial sites, binding to the alkali and alkaline earth metals, the Chlorella@Mn catalyst surface naturally carried a spectrum of acidic species (such as SO42−, PO3−, SiO32−), proficient in capturing alkali/alkaline earth metal effectively, elements such as S, P, and Si formed bonds with K, Na, Ca, and Mg. The synergistic protection of the active sites and the surface elements avoided the deactivation of the catalyst. The detrimental effects of high concentrations of alkali and alkaline earth metals were primarily due to promoting an excessively high valence state of Mn on the catalyst surface and the reduction or loss of NH3 adsorption and activation at Brønsted acid sites. This research provided valuable insights for advancing the development of low-temperature denitration catalysts with improved resistance to alkali and alkaline earth metal poisoning.

Efficient removal of aqueous ciprofloxacin antibiotic by ZnO/CuO-bentonite composites synthesized via carbon-bed pyrolysis of bentonite and metal co-precipitation

Antibiotics are of emerging concern due to their widespread use, lack of adequate treatment, and for their potential to threaten human health and the environment. Here, a facile fabrication approach for synthesizing ZnO/CuO-bentonite composites was investigated via carbon-bed pyrolysis of bentonite followed by ZnO/CuO co-precipitation. Sorbents were synthesized using a range of bentonite pyrolysis temperatures, metal oxide contents, and ZnO:CuO mass ratios. The ZnO/CuO-bentonite composites exhibited diverse functional groups, excellent mesoporosity, and high specific surface area (135.0 m2 g−1, four times that of pyrolyzed bentonite-only control). Ciprofloxacin removal was maximized at a bentonite pyrolysis temperature of 450 °C, a total metal oxide content of 25 %, and a Zn/Cu ratio between 95:5 and 93:7, and this material had an observed experimental CIP adsorption of 451 mg g−1 and a calculated maximum adsorption capacity of 1249.3 mg g−1. This excellent CIP sorption ability was attributed to its abundant surface active sites and multiple sorption mechanisms, including hydrogen-bond interaction, ion exchange, and electrostatic interaction. These results illustrate that ZnO/CuO-bentonite composite sorbents have excellent potential for use in environmental remediation and water treatment applications.

Effect of Metal Oxide Deposition on the Sensitivity and Resolution of E-Beam Photoresist.

Organic-inorganic hybrid resists offer a solution to the issue of low sensitivity in organic photoresists like poly(methyl methacrylate) (PMMA). In this study, an organic-inorganic hybrid resist (PMMA-Al2O3) with high sensitivity and resolution was prepared by depositing metal oxides into PMMA using sequential infiltration synthesis (SIS). PMMA-Al2O3 was prepared by precisely controlling the number of SIS cycles (<23) in various atomic layer deposition (ALD) processes to facilitate the growth of metal oxides within PMMA pores. The impact of different metal oxide contents and distributions on the sensitivity and resolution of electron beam exposure was investigated. Numerical simulations of the deposit formation within the PMMA pores were performed by solving the pore-scale ALD governing equations fed by the reactor-scale boundary conditions. The gradual pore constriction with SIS cycles was predicted and validated by the experimental charaterizations. The results demonstrated that PMMA-Al2O3 was prepared using 20 SIS cycles, which corresponds to the numerically predicted occurrence of the pore blockage at the upper region of the PMMA layer, exhibiting optimal electron beam (e-beam) resolution while enabling line exposure with a width of 50 nm. While the corresponding sensitivity was lower than those of the samples prepared using 5 and 10 SIS cycles, the degradation of the PMMA structure was affected under exposure. The pattern transfer results showed that the line width was well retained for 20 cycles of deposition because of the high etching resistance of Al2O3. This research is expected to provide an effective approach to developing next-generation high-performance photoresists.

Direct aqueous mineral carbonation of secondary materials for carbon dioxide storage

Mineral carbonation of secondary materials offers an innovative way of storing carbon dioxide in materials that instead would mostly go to waste. This study investigates the carbonation efficiency (CE) of 11 different secondaries from refractory production, waste incineration, and the paper industry compared to untreated and thermally activated serpentinite. To determine the chemical and mineralogical composition of the materials, various analytical methods, like X-ray fluorescence, X-ray diffraction, scanning electron microscopy, Brunauer-Emmet-Teller and thermogravimetric analysis have been employed, both before and after the direct aqueous carbonation process. Each material was examined over reaction times of 6 & 10 hours at 180 °C and a starting pressure of 20 bar in a 0.6 L stainless steel batch reactor. The received results were then compared to the theoretical CO2 uptake, defined as the maximum carbon dioxide storage potential achievable if all Ca, Fe and Mg ions were converted to carbonates. The findings indicate carbonation efficiencies of 14–65 % for secondary materials, compared to 0.7–14 % observed in the serpentinite samples. The highest uptakes were achieved by the refractory materials, primarily due to their high metal oxide content. However, a negative impact was observed from graphite-based carbon binders in the refractories, with increased leaching of these binders leading to a decrease in carbonation efficiency. Materials with higher SiO2 content showed reduced performance, suggesting a passivation layer buildup during carbonation.

Efficiency, characterization, and kinetics during removal of COS and H2S in gasified syngas by red soil

Application of red soil in dry desulfurization process for removal of H2S and COS from coal gasified gas is preferable due to its metal oxides content, sustainability, and low cost. This study examined the performance of several red soil types around Taiwan, including Loupi/LP, Houdi/HD, and Dadusan/DDS for removal of COS and H2S. LP red soil presented the best removal efficiency with 91.8 % utilization value and chosen in further assessment on the performance under various operating conditions and cycle test. Moreover, this study was also aimed to explore the type of active metal oxides for removal of COS and H2S, along with the reaction kinetics and exhausted gas analysis after the process. The presence of iron oxides in LP red soil beneficially supported the removal of COS and H2S. Moreover, increasing of CO content in the syngas prolonged the breakthrough time and utilization value. On the other side, higher H2 content triggered the occurrence of water–gas-shift reaction. The cycle test indicated sintering process due to intense reaction under high temperature which led to deterioration of performance. Analysis of reaction kinetics using both Type I and Type II deactivation models indicated their well fitting data with the data of this study.

Thermoluminescence characteristics of gamma-irradiated Gd:Mg doped silica glass

This study explores the characteristics of thermoluminescence (TL) yield of silica glass doped with Gd2O3 and MgO for dosimetry via sol-gel route, with varying concentrations of rare earth metal oxides, ranging from 0.1 to 0.8 mol%. Gamma irradiation was delivered using 1.25 MeV 60Co, with entrance doses of 2–10 Gy. The characterization of Gd:Mg-doped SiO2 included assessing TL dose response, sensitivity, linearity index, glow curve, and fading. It has been found that 0.2 mol% Gd:Mg-doped SiO2 shows promising TL dosimetric properties due to its high linearity, high sensitivity, and low thermal fading. In addition, it demonstrated exceptional dosimetric response across the entire dose range studied, with a coefficient of determination R2 exceeding 91%. A computerized glow curve deconvolution method was conducted to determine the kinetic parameters by using Glowfit software. The glow curves include five peaks associated with activation energies and frequency factors with values 0.88–2.42 eV and 5.58 × 106–7.22 × 1026 s−1, respectively. The 0.2 mol% Gd:Mg-doped SiO2 demonstrates minimal fading effects, retaining a significant portion of the TL signal with ∼33% of the initial signal lost over 28 days post-irradiation. The results indicate that the Gd:Mg-doped SiO2 offers a promising performance as a low-cost passive radiation dosimeters.

Effect of metal oxide contents on the structure and performance of spray-dried CrVO4/SiO2 catalysts for the ammoxidation of chlorotoluenes

Effect of metal oxide contents on the structure and performance of spray-dried CrVO4/SiO2 catalysts for the ammoxidation of chlorotoluenes

A high-resolution characterization of surface film formed on alloys 800 and 690 exposed to chloride and thiosulfate-containing solution at 300°C

PurposeThis paper aims to characterize the surface film formed on Alloys 800 and 690 in chloride and thiosulfate-containing solution at 300°C.Design/methodology/approachAlloy 800 and 690 were immersed in chloride and thiosulfate-containing solution at 300°C up to five days, and then the surface film was analyzed by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM) and energy dispersive X-ray spectrometers (EDX).FindingsThrough static immersion experiments in a high-temperature and high-pressure water environment, the alloy samples covered by surface film after five days of immersion were obtained. The morphology of the surface film was characterized at both horizontal and cross-sectional scales using SEM and focused ion beam-TEM techniques. It was observed that due to the influence of the quartz lining, the surface film primarily exhibited a bilayered structure. The first layer contained a significant amount of SiO2, with a higher content of metal hydroxides compared to metal oxides. The second layer was predominantly composed of Fe, Ni and Cr, with a higher content of metal oxides compared to metal hydroxides.Originality/valueThe results showed that the materials of the lining of the autoclave could significantly influence the film composition of the tested material, which should be paid attention when analyzing the corrosion mechanism at high temperature.

A Comparison of Different Protocols for the Extraction of Microbial DNA Inhabiting Synthetic Mars Simulant Soil.

Compared with typical Earth soil, Martian soil and Mars simulant soils have distinct properties, including pH > 8.0 and high contents of silicates, iron-rich minerals, sulfates, and metal oxides. This unique soil matrix poses a major challenge for extracting microbial DNA. In particular, mineral adsorption and the generation of destructive hydroxyl radicals through cationic redox cycling may interfere with DNA extraction. This study evaluated different protocols for extracting microbial DNA from Mars Global Simulant (MGS-1), a Mars simulant soil. Two commercial kits were tested: the FastDNA SPIN Kit for soil ("MP kit") and the DNeasy PowerSoil Pro Kit ("PowerSoil kit"). MGS-1 was incubated with living soil for five weeks, and DNA was extracted from aliquots using the kits. After extraction, the DNA was quantified with a NanoDrop spectrophotometer and used as the template for 16S rRNA gene amplicon sequencing and qPCR. The MP kit was the most efficient, yielding approximately four times more DNA than the PowerSoil kit. DNA extracted using the MP kit with 0.5 g soil resulted in 28,642-37,805 16S rRNA gene sequence reads and 30,380-42,070 16S rRNA gene copies, whereas the 16S rRNA gene could not be amplified from DNA extracted using the PowerSoil kit. We suggest that the FastDNA SPIN Kit is the best option for studying microbial communities in Mars simulant soils.

The effects of metal-oxide content in MnO2-activated carbon composites on reactive adsorption and catalytic oxidation of formaldehyde and toluene in air

The deterioration in air quality caused by volatile organic compounds (VOCs) has become an important environmental issue. Here, activated carbon (AC) composites with manganese oxide (MnO2: 1 % to 50 %) are synthesized as MAC for the removal of formaldehyde (FA) and toluene in air through a combination of reactive adsorption and catalytic oxidation (RACO) at room temperature (RT). The best-performing composite (MAC-20: 20 % of MnO2) exhibits a 10 % breakthrough volume (BTV10%) of FA and toluene at 41.2 and 377 L g−1, respectively while realizing complete oxidation of FA and toluene into carbon dioxide (CO2) at 100 °C and 275 °C, respectively. The reaction kinetic rates (r) for 10 % removal efficiency of FA and toluene (XFA or T) at RT are estimated as 9.82E-02 and 3.20E-02 mmol g−1 h−1, respectively. The high performance of MAC-20 can be attributed to its enriched adsorption capacity of oxygen vacancy (OV) and the presence of adsorbed oxygen (OA), as shown by an Mn3+/Mn4+ ratio of 0.729 and an OA/lattice‑oxygen (OL) ratio of 1.50. The results of this study highlight the interactive roles of oxygen abundance and temperature in the generation of distinctive oxidation patterns for FA in reference to toluene. This study is expected to offer practical guidance for the implementation of RACO against diverse VOCs for efficient management of air quality.

PVA-TiO2 Nanocomposite Hydrogel as Immobilization Carrier for Gas-to-Liquid Wastewater Treatment

This study investigates the development of polyvinyl alcohol (PVA) gel matrices for biomass immobilization in wastewater treatment. The PVA hydrogels were prepared through a freezing–thawing (F-T) cross-linking process and reinforced with high surface area nanoparticles to improve their mechanical stability and porosity. The PVA/nanocomposite hydrogels were prepared using two different nanoparticle materials: iron oxide (Fe3O2) and titanium oxide (TiO2). The effects of the metal oxide nanoparticle type and content on the pore structure, hydrogel bonding, and mechanical and viscoelastic properties of the cross-linked hydrogel composites were investigated. The most durable PVA/nanoparticles matrix was then tested in the bioreactor for the biological treatment of wastewater. Morphological analysis showed that the reinforcement of PVA gel with Fe2O3 and TiO2 nanoparticles resulted in a compact nanocomposite hydrogel with regular pore distribution. The FTIR analysis highlighted the formation of bonds between nanoparticles and hydrogel, which caused more interaction within the polymeric matrix. Furthermore, the mechanical strength and Young’s modulus of the hydrogel composites were found to depend on the type and content of the nanoparticles. The most remarkable improvement in the mechanical strength of the PVA/nanoparticles composites was obtained by incorporating 0.1 wt% TiO2 and 1.0 wt% Fe2O3 nanoparticles. However, TiO2 showed more influence on the mechanical strength, with more than 900% improvement in Young’s modulus for TiO2-reinforced PVA hydrogel. Furthermore, incorporating TiO2 nanoparticles enhanced hydrogel stability but did not affect the biodegradation of organic pollutants in wastewater. These results suggest that the PVA-TiO2 hydrogel has the potential to be used as an effective carrier for biomass immobilization and wastewater treatment.

An XAS study of Hg(II) sorption to Al-based drinking water treatment residuals

Drinking water treatment residuals (DWTRs) are produced from the coagulation and flocculation processes in conventional drinking water treatment. The abundant metal oxide content of these materials resulting from the use of coagulants, like alum and ferric chloride, has driven strong research interest into the reuse of DWTRs as sorptive materials. Using a suite of aluminum-based DWTRs, we provide new insights into Hg(II) sorption mechanisms. Experiments performed at circum-neutral pH show that sorption capacities are related to the amount of organic carbon/matter present in DWTRs. We found that carbon rich samples can scavenge about 9000 mg/kg of Hg, in contrast to 2000 mg/kg for lime based DWTRs. X-ray absorption spectroscopy (XAS) at the Hg L3 edge further characterizes mercury coordination. X-ray absorption near edge structure (XANES) and extended x-ray absorption fine structure (EXAFS) results point to a partial association of mercury with sulfur at low mass loadings, transitioning to a full association with oxygen/carbon at higher concentrations of sorbed Hg(II) and in DWTRs with limited sulfur content. These results suggest that sorption of Hg(II) is primarily controlled by the carbon/organic matter fraction of DWTRs, but not by the coagulants.

A comparative study on the surface chemistry and electronic transport properties of Bi2Te3 synthesized through hydrothermal and thermolysis routes

Bismuth telluride-Bi2Te3 is the most promising material for harvesting thermal energy near room temperature. There are numerous works on Bi2Te3 reporting significantly different transport properties, with no clear connection to the synthetic routes used and the resultant surface chemistry of the synthesized materials. It is of utmost importance to characterize the constituent particles’ surface and interfaces to get a better understanding of their influence on the transport properties, that will significantly improve the material design starting from the synthesis step. Electrophoretic deposition (EPD) is a promising technique, enabling the formation of thick films using colloidally stabilized suspensions of pre-made nanoparticles, which can enable the study of the effect of surface chemistry, in connection to the synthetic route, on the material’s transport properties. In order to explore the differences in surface chemistry and the resultant transport properties in relation to the synthetic scheme used, here we report on Bi2Te3 synthesised through two wet-chemical routes in water (Hydro-) and oil (Thermo-) as the solvents. XRD analysis showed a high phase purity of the synthesized materials. SEM analysis revealed hexagonal platelet morphology of the synthesized materials, which were then used to fabricate EPD films. Characterization of the EPD films reveal significant differences between the Hydro- and Thermo-Bi2Te3 samples, leading to about 8 times better electrical conductivity values in the Thermo-Bi2Te3. XPS analysis revealed a higher metal oxides content in the Hydro-Bi2Te3 sample, contributing to the formation of a resistive layer, thus lowering the electrical conductivity. Arrhenius plots of electrical conductivity vs inverse temperature was used for the estimation of the activation energy for conduction, revealing a higher activation energy need for the Hydro-Bi2Te3 film, in agreement with the resistive barrier oxide content. Both the samples exhibited negative Seebeck coefficient (S) in the order of 160–170 mV/K. The small difference in S of Hydro- and Themo-Bi2Te3 films was explained by the effective medium theory, revealing that the magnitude of S is linearly correlated with the surface oxide content. Based on the findings, TE materials synthesized through thermolysis route is recommended for further studies using soft treatment/processing of pre-made TE materials. EPD platform presented here is shown to clearly expose the differences in the electronic transport in connection to nanoparticle surface chemistry, proving a promising methodology for the evaluation of morphology, size and surface chemistry dependence of electronic transport for a wide range of materials.

Single-Step Formation of Metal Oxide Nanostructures Wrapped in Mesoporous Silica and Silica–Niobia Catalysts for the Condensation of Furfural with Acetone

The integration of metal oxide nanomaterials with mesoporous silica is a promising approach to exploiting the advantages of both types of materials. Traditional synthesis methods typically require multiple steps. This work instead presents a fast, one-step, template-free method for the synthesis of metal oxides homogeneously dispersed within mesoporous silica, including oxides of W, Ti, Nb, Ta, Sn, and Mo. These composites have tunable metal oxide contents, large surface areas, and wide mesopores. The combination of Nb2O5 nanoparticles (NPs) with SiO2 results in an increased surface area and a larger number of acid sites compared to pure Nb2O5 NPs. The surface texture and acidity of the silica–niobia composites can be tuned by adjusting the Nb/Si molar ratio. Moreover, the silica provides protection to the niobia NPs, preventing sintering during thermal treatment at 400 °C. The silica–niobia materials exhibit superior performance as catalysts in the aldol condensation of furfural (Fur) with acetone compared to pure niobia, leading to an up to 62% in product yield. Additionally, these catalysts show remarkable stability, retaining their performance over multiple runs. This work demonstrates the potential of the proposed synthesis approach for preparing more sustainable, high-performance, durable, and stable nanoscale metal oxide-based catalysts with a tunable composition, surface area, and active site density.

Synthesis and characterization of functionally graded SiC-mullite thermal material

SiC-mullite is considered for high temperature applications due to its high mechanical strength and thermal shock-resistance. However, maintaining these properties is challenged by the high processing temperature requirement for the formation and densification of the mullite phase which leads to abundant surface oxidation of SiC into cristobalite. Cristobalite has relatively poor mechanical strength and thermal properties compared to SiC. Herein, we report on using coal fly ash as a source of alumina (Al2O3) that reacts in situ with the silica (SiO2), oxidation product of SiC. The instantaneous mullite formation on the surface of SiC facilitated due to the presence of minor concentrations of metal oxides in coal fly ash, resulted in a strong bonding zone between the two phases at relatively low temperature. In this work, SiC was mixed with coal fly ash at weight ratios of 90SiC/10ash, 85SiC/15ash, 80SiC/20ash, and 75SiC/25ash and sintered at 1400 °C. Measurements of mechanical properties showed that the 85SiC/15ash composition had the highest mechanical strength among samples. XRD analysis showed the phase composition of thermally treated 85SiC/15ash to be 81.8 wt% SiC, 11.4 wt% mullite, and 6.8 wt% cristobalite. SEM-EDX revealed a concentration gradient of Al in the cristobalite which enhanced formation of functionally graded bonding zones between phases and resulted in SiC-mullite composite with high thermomechanical properties. The compressive strength, nanoindentation elastic modulus, and Vickers hardness were 434 ± 20 MPa, 370.9 ± 22.6 GPa, and 11.5 ± 1.2 GPa respectively. The thermal shock resistance test showed high dimensional and mechanical stabilities after quenching in liquid nitrogen (−196 °C) from 1400 °C. The SiC-mullite composite showed low thermal expansion co-efficient from 3.17 × 10−7/K to 5.615 × 10−6/K when the sample was heated from 182 K to 354 K. The specific heat capacity, thermal diffusivity, and thermal conductivity were 7.83 ± 0.0014 J/g.K, 1.04 ± 0.013 mm2/s, and 17 W/m.K at 100 °C, respectively. The SiC-mullite composite exhibited moderate electrical conductivity of 3.48 × 10−2 S/m at 1000 °C.

Hydrothermal synthesis of high-purity zeolite X from coal fly ash for heavy metal removal: Kinetic and isotherm analysis

Treated fly ash (TCFA) yielded high-purity, single-phase zeolite-X, efficiently removing Ni and V ions from aqueous solutions. The pretreatment process of raw fly ash (RCFA) involved magnetic fraction separation, followed by acid washing. Zeolites were synthesized by the fusion prior step to the hydrothermal treatment method. The VSM test shows that the MS value dropped from 2.19 to 1.43 emu/g due to removing the magnetic fraction. These findings align with XRF results showing a 98 % reduction in Fe2O3 content, while acid washing lowered other metal oxide content to below 12 %. XRD results indicate the successful synthesis of high-crystallinity, single-phase zeolite X-TCFA, achieved at 90 °C for 12 h. SEM images further confirm the purity of the product, revealing pyramidal octahedral-shaped single crystals. Additionally, BET analysis shows a high surface area of 452 m2/g, featuring mesopores from 2 to 50 nm. The FTIR spectrum displayed the characteristic peaks of Zeolite X, confirming the success of the preparation process. TCFA-zeolite X has high thermal stability based on TGA analysis. The pseudo-second-order model fits the kinetic data, suggesting that chemical adsorption mechanisms control Ni and V adsorption. Langmuir isotherm best-explained results, with max adsorption of 41.55 mg/g Ni and 32.38 mg/g V.

Analysis of asymmetrical supercapacitor with horizontally configured electrodes

Energy is available in several forms but its use to humans is predominantly in the electrical form. Since electrical energy is not immediately consumed post conversion, energy storage devices are required for its storage. This reinforces the importance of research in electrical energy storage devices. Till date, very few energy storage devices have been developed for commercial use. Asymmetrical supercapacitors are the newest addition to this list and have the potential to replace conventional energy storage devices in times to come. They can be further classified based on their electrode orientation namely horizontally and vertically configured electrodes. Research has been conducted on asymmetrical supercapacitors with horizontally configured electrodes as they have a better performance over vertically configured electrode. Analysis of asymmetrical supercapacitor with horizontally configured electrodes through statistical modelling approach is presented in the paper which is useful in setting electrode parameter values during the manufacture of this device. Electrode material loading on current collector of both electrodes is found to be affecting specific-capacitance values; they also add to nonlinearity in the device. Metal oxide contents are an addition to the interaction effect. Modelling approach adopted has provided better insights as to how various electrode parameters interact and in turn affect the specific capacitance. Presented research work also brings out need of extra negative plate or bigger size negative plate in asymmetrical supercapacitors. Findings of this research work can be used as basis for study of other electrical energy storage devices such as battery, fuel cell etc.

Microbial pathways driving stable soil organic carbon change in abandoned Moso bamboo forests in southeast China

Mineral-associated organic carbon (MOC) is a stable component of the soil carbon (C) pool, critical to realize carbon sequestration and coping with climate change. Many Moso bamboo (Phyllostachys edulis) forests in subtropical and tropical areas that used to be intensively managed have been left unmanaged. Still, studies on MOC changes occurring during the transition from intensive management to unmanagement are lacking. Besides, the understanding of the role of microorganisms in MOC accumulation is far from satisfactory. Based on the combination of field investigation and laboratory analysis of 40 Moso bamboo forest sampling plots with different unmanaged chronosequence's in southeast China, we observed the MOC content in Moso bamboo forests left unmanaged for 2–5 years had decreased, whereas that in forests left unmanaged for 11–14 years had increased compared with that in intensively managed forests. Specifically, the MOC contents in forests left unmanaged for 11–14 years were significantly higher than in those under intensive management or unmanaged for 2–5 years. Moreover, we found that microorganisms drove MOC change through two different pathways: (i) more microorganisms led to more soil nutrients, which led to more amino sugars, ultimately resulting in the accumulation of MOC, and (ii) microorganisms promoted the accumulation of MOC by influencing the content of metal oxides (poorly crystalline aluminum oxides and free aluminum oxides). We believe that ignoring the interaction between microorganisms and metal oxides may lead to uncertainty in evaluating the relative contribution of microbial residues to MOC.

Soil Organic Carbon and Total Nitrogen Stocks and Interactions with Soil Metal Oxides in Different Climatic Zones

Studying both soil carbon (C) and nitrogen (N) storages in different climate zones and their relationship with climatic factors is of great significance for understanding soil fertility and predicting global climate change. Climate influences soil minerals, which are important for soil organic carbon (SOC) and N retention. However, there are few studies on SOC and soil total nitrogen (STN) storage in different climatic zones, and of the effects of soil oxidation minerals on SOC and STN storage. We measured the storage of SOC and STN and the content of oxidizable minerals in soils from different climatic regions, then obtained climate data from the China Meteorological Data Service Center, and finally investigated the effects of climate factors and soil oxides minerals on SOC and STN. The results showed that climatic factors (mean annual temperature—MAT, mean annual precipitation—MAP, and ≥10 °C mean annual cumulative temperature—MACT) had significant effects on SOC and STN content, and there was significant epistatic clustering of SOC and STN contents in different climatic zones. When MAT, MAP, and MACT increased, SOC and STN storage showed a trend of increasing and then decreasing, and both SOC and STN storages were largest in the middle temperate zone. The content of soil metal oxides (Al2O3, Fe2O3, Na2O, MgO, CaO, K2O, and TiO2) showed significant positive correlation with climatic factors (MAT, MAP, and MACT). The contents of Al2O3, Fe2O3, CaO, K2O, and TiO2 showed significant negative correlation with SOC and STN contents. In summary, our results showed that, although soil metal oxides (SMO) have a protective effect on SOC and STN to some extent, they do not change the influence of climatic factors on SOC and STN storage.