High-temperature Activation Research Articles

Preliminary investigation of the effects of high-temperature thermal activation on the activity of graphite tailings and the mechanical properties of graphite tailings mortar

The disposal of graphite tailings, a byproduct of graphite mining, poses significant recycling challenges. This study explores eco-friendly cement mortar by partially replacing sand with activated graphite tailings, focusing on waste utilization. Activating the pozzolanic properties of graphite tailings at various thermal activation temperatures converts them into high-quality binder materials. Quantitative assessments of graphite tailings' activity, conducted through ion leaching tests and raw material diffraction analysis, produce an activity index Ka, evaluating their performance under different thermal activation temperatures. Variable testing of substitution rates and activation temperatures examines changes in mechanical properties, microstructure, and pore distribution of the graphite tailings mortar. Optimum results reveal a 30 % substitution rate and a 750°C activation temperature. Graphite tailings, as pozzolanic binder materials, enhance mortar strength by improving particle size distribution, reducing "micro-area bleeding" and "boundary effects". After thermal activation, reactive minerals on the tailings' surface undergo secondary hydration reactions with cementitious products, modifying chemical structures and micro-morphology at the interface. Semi-quantitative XRD analysis and FT-IR spectroscopy characterize the ensuing chemical reactions, unveiling molecular bond and functional group changes. The superior performance of thermally activated graphite tailings primarily stems from increased active SiO2 and Al2O3 post-activation. The active SiO2 and Al2O3 reacts with cementitious products to form C-(A)-S-H gels, filling micro-pores at the tailings-mortar interface, which is the key characteristic that enables graphite tailings to serve as high-quality pozzolanic binder aggregates. A predictive model for compressive strength, utilizing reference models from solid waste mortar concrete, quantifies the positive impact of chemical activation. The theoretical results obtained from this predictive model closely align with the experimental findings.

Characterize the high-temperature steady-state rheological behavior and Arrhenius activation of PEEK via strain rate jump tensile tests

Polyetheretherketone (PEEK) is a high-performance thermoplastic polymer with diverse industrial applications, such as aerospace, automotive, electronics, and medical devices. However, systematic research on its high-temperature rheological characteristics is inadequate. In this study, strain rate jump tensile tests were introduced to examine the steady-state rheology phenomena and strain rate sensitivity of PEEK at four different temperatures and nine different strain rates. Theoretical analysis based on the free volume theory and the Arrhenius law was also carried out to further analyze the transition of PEEK from Newtonian flow to non-Newtonian flow. Results indicate that PEEK materials exhibit a transition from Newtonian flow to non-Newtonian flow similar to metal materials at high temperatures. The transition point from Newtonian flow to non-Newtonian flow is marked by the emergence of steady-state rheology and its characteristic stress. Theoretical analysis demonstrates that the transition of PEEK is in accordance with the Arrhenius low. Moreover, its apparent activation energy (1.42 eV) is significantly lower than that of metal materials (5.28 eV), indicating a lower energy barrier and an easier transition. The strain rate sensitivity index correlates negatively with rising temperatures, especially at lower rates. This study enhances understanding of PEEK's rheological characteristics at high temperatures, aiding the development and application of high-performance thermoplastic materials.

Local and regional enhancements of CH4, CO, and CO2 inferred from TCCON column measurements

Abstract. In this study, we demonstrate the utility of available correlative measurements of carbon species to identify regional and local air mass characteristics as well as their associated source types. In particular, we combine different regression techniques and enhancement ratio algorithms with carbon monoxide (CO), carbon dioxide (CO2), and methane (CH4) total column abundance from 11 sites of the Total Carbon Column Observing Network (TCCON) to infer relative contributions of regional and local sources to each of these sites. The enhancement ratios provide a viable alternative to univariate measures of relationships between the trace gases that are insufficient in capturing source-type and transport signatures. Regional enhancements are estimated from the difference between bivariate regressions across a specific time window of observed total abundance of these species (BERr for bulk enhancement regression ratio) and inferred anomalies (AERr for anomaly enhancement regression ratio) associated with a site-specific background. Since BERr and AERr represent the bulk and local species enhancement ratio, respectively, its difference simply represents the site-specific regional component of these ratios. We can then compare these enhancements for CO2 and CH4 with CO to differentiate between combustion and non-combustion air masses. Our results show that while the regional and local influences in enhancements vary across sites, dominant characteristics are found to be consistent with previous studies over these sites and with bottom-up anthropogenic and fire emission inventories. The site in Pasadena shows a dominant local influence (> 60 %) across all species enhancement ratios, which appear to come from a mixture of biospheric and combustion activities. In contrast, Anmyeondo shows more regionally influenced (> 60 %) air masses associated with high-temperature and/or biofuel combustion activities. Ascension Island appears to only show a large regional influence (> 80 %) on CO / CO2 and CO / CH4, which is indicative of transported and combustion-related CO from the nearby African region, consistent with a sharp rise in column CO (3.51 ± 0.43 % ppb yr−1) at this site. These methods have important applications to source analysis using spaceborne column retrievals of these species.

Transforming tire-derived char into powerful arsenic adsorbents by mild modification

A large amount of arsenic-containing wastewater discharged by the non-ferrous metal industry will cause serious environmental problems if it is not properly treated. Pyrolysis char of waste tire is a kind of solid waste. Since the surface properties of tire derived char (TC) are affected by tar/ash adhesion during pyrolysis, it is necessary to modify TC to treat wastewater containing As(V) effectively as an adsorbent. At present, most studies on the modification of TC are prepared into activated carbon by high temperature activation in N2 atmosphere. In this study, TC was modified at room temperature and air atmosphere, and Fe(OH)3-TCNaOH adsorbent with particle size of 61–75 μm was obtained under the premise of the removal rate of As(V) and the settling performance of the adsorbent. When the initial concentration of As(V) was 5 mg/L, the removal rate of As(V) by Fe(OH)3-TCNaOH with a particle size of 61–75 μm could reach 90% within 30 min under a wide pH range (3–9). The adsorption of As(V) by Fe(OH)3-TCNaOH was most affected by the coexistence of PO43-, which resulted in the removal rate of As(V) decreased by about 20%. The adsorption mechanism shows that the significant increase in the number of 3–5 nm mesoporous pores of Fe(OH)3-TCNaOH and the formation of H bonds are beneficial to the adsorption of Fe(OH)3-TCNaOH to As(V), and improve the stability of Fe-As complex.

Identification and biochemical characterization of a novel halolysin from Halorubellus sp. PRR65 with a relatively high temperature activity.

Extracellular proteases from haloarchaea, also referred to as halolysins, are in increasing demand and are studied for their various applications in condiments and leather industries. In this study, an extracellular protease encoding gene from the haloarchaeon Halorubellus sp. PRR65, hly65, was cloned and heterologously expressed in E. coli. The novel halolysin Hly65 from the genus Halorubellus was characterized by complete inhibition of phenylmethanesulfonyl fluoride (PMSF) on its enzyme activity. Experimental determination revealed a triad catalytic active center consisting of Asp154-His193-Ser348. Deletion of the C-terminal extension (CTE) resulted in loss of enzyme activity, while dithiothreitol (DTT) did not inhibit the enzyme activity, suggesting that Hly65 may function as a monomer. The Km, Vmax and Kcat for the Hly65 were determined to be 2.91mM, 1230.47 U·mg-1 and 1538.09 S-1, respectively, under 60°C, pH 8.0 and 4.0M NaCl using azocasecin as a substrate. Furthermore, a three-dimensional structure prediction based on functional domains was obtained in this study which will facilitate modification and reorganization of halolysins to generate mutants with new physiological activities.

Porous nitrogen-doped carbons derived from poultry feathers for electrochemical capacitors

The synthesis of a nitrogen doped carbon material (NDCM) from the ball-milling and chemical activation of high temperature carbonised waste chicken feathers is reported. Synthesised NDCMs with nitrogen content ranging from 2.2 to 6.6 wt% were analysed via a range of physio and electrochemical characterisation methods. The effects of carbonisation temperature, mechanical milling and chemical activation were evaluated on specific capacitance and charge retention. Electrochemical testing demonstrated that the optimised NDCM (carbonised at 700 °C followed by ball milling and chemical activation) possessed a specific capacitance of 195 F g−1 at 1 A g−1 current density. At the higher current density of 40 A g−1 89 % of the capacitance is retained. Moreover, this material showed a cycle life of 1000 galvanostatic charge/discharge cycles with a 1 % loss in capacitance at a current density of 5 A g−1.

Coal-based Si self-doped disordered porous carbon for supercapacitor electrodes

In preparing activated carbon for coal-based supercapacitors, silicon in coal usually requires removal with hydrofluoric acid, which is neither economical nor environmentally friendly. However, silicon can be used as the anode in lithium batteries due to its high theoretical capacity. So silicon was retained to study its effect on supercapacitors. By retaining silicon without hydrofluoric acid treatment and activating at lower temperature, the prepared Si-doped activated carbon achieved a high specific capacitance of 318.3F/g at 0.5 A/g in the three-electrode test system. Omitting hydrofluoric acid treatment increased the specific capacitance by 49 %. Experimental results show that this 4.92 % silicon doping, mainly CSiO3, is the main reason for the enhancement. Density functional theory (DFT) simulations confirmed that CSiO3 improves double-layer capacitance by localizing surface charge and enhancing electrolyte ion adsorption, while also boosting quantum capacitance. High activation temperatures increase coal-activator reactions but also decrease disorder of the carbon, reducing specific capacitance. Temperature experiments show that the specific capacitance increases and then decreases in the range of 600 ∼ 950 °C, and reaches a peak at 650 °C. This study presents a simple, effective method to enhance supercapacitor performance with silicon-carbon precursors and provides detailed explanation on the capacitance enhancement mechanism for the first time.

Fe2O3/In2O3 composite materials for dual-selective detection of H2S and NO2: Study on sensing mechanisms and sensing transition

Developing concise and efficient dual-selective gas sensors has been a significant challenge in sensing technology. In this study, a Fe2O3/In2O3 (FIO) composite material was successfully synthesized via a water bath method for highly efficient dual-selective detection of H2S and NO2. The enhanced dual-selectivity of the composite material is attributed to the high-quality heterojunction formed at the Fe2O3 and In2O3 interface, which provides more active sites and optimizes the electronic structure, thereby greatly improving electron transport efficiency. Consequently, this unique structure significantly enhances the gas sensing response and stability of the composite material. The optimal FIO-3 composite shows significant responses: 14.7 at 80 °C with 100 ppm H2S and 64.3 at 100 °C with 700 ppb NO2, achieving 7- and 31-fold improvements over pure Fe2O3. Analysis indicates that the dual-selective response of the FIO composite material is attributed to synergistic enhancement mechanisms, primarily controlled by high-temperature activation effects. Further density functional theory (DFT) studies reveal changes in charge density at the composite material interface, particularly facilitated by the formation of oxygen bridges promoting electron transfer from In2O3 to Fe2O3. This study offers new insights into the sensing transition of dual-selective gas sensors.

Activation technology of steel slag for concrete exposed to plateau climate: a state-of-the-art review.

As a byproduct of steelmaking, steel slag occupies significant land resources and poses potential environmental and safety challenges due to its extensive accumulation. Recently, steel slag has shown promising applications in the field of concrete. However, considering the complexity of the plateau environment, the utilization of steel slag is relatively lacking, and its low reactivity and poor volume stability remain the main factors restricting its application in plateau concrete. This paper reviews the research status of steel slag activation techniques for concrete, including wet grinding, chemi-excitation, high-temperature activation, and carbonation treatment. The effects of different treatment techniques on the mechanical and durability properties of concrete and the potential issues are discussed. Although different modification methods can improve the activity and volume stability of steel slag to varying degrees, a single modification technology is difficult to achieve the high-quality utilization of steel slag in concrete on the plateau. Based on this, a steel slag grading grinding-magnetic separation utilization technique suitable for high-altitude areas is proposed, which is beneficial for improving the added value and utilization rate of steel slag in concrete.

Petrogenesis of magmatic charnockite-biotite granite suite from parts of the Chotanagpur Granite Gneissic Complex (CGGC), eastern Indian shield: Implication for the break down of the Columbia Supercontinent

A rare porphyritic charnockite that is girdled by and mineralogically grades to biotite granite occurs as a part of the Chotanagpur Granite Gneissic Complex (CGGC) in and around Massanjore, Jharkhand, India. Preservation of certain textural features, including (a) euhedral to subhedral grains of orthopyroxene, (b) low dihedral angle subtended by orthopyroxene and plagioclase grains, and (c) relict intergranular and porphyritic textures, are consistent with the view that orthopyroxene in the studied rocks has a magmatic origin. Preserved magmatic features and other petrological attributes of these rocks do not support any significant mass change beyond a few tens of microns during the overprinting high-grade metamorphism. The geochemical variation of the felsic rock suite (porphyritic charnockite and biotite granite) indicates that they are cogenetic and are derived from a ferroan A-type granitoid magma by crystal fractionation. The observed geochemical trend of the studied felsic rock suites has been simulated by phase equilibria modelling in the open system using the system components Na2O-CaO-K2O-FeO-MgO-Al2O3-SiO2-H2O-TiO2-O2. The observed mineralogical and geochemical attributes and the results of the modelling study are consistent with a petrogenetic process in which high magma temperature (> 900 °C), low pressure, and low water activity in the parental melt favoured the separation of an orthopyroxene bearing cumulate assemblage (orthopyroxene + plagioclase + quartz + K-feldspar + ilmenite + magnetite) in the initial part of the magmatic differentiation. Removal of this anhydrous cumulitic assemblage raised the bulk H2O content in the residual melt. Orthopyroxene became unstable with respect to biotite in the evolved melt that eventually crystallised minerals that formed the biotite granite. An increase in magma fO2 also restricts the orthopyroxene stability in felsic magma. Taken together all the petrological and geochemical attributes, we demonstrate that fractionation of an orthopyroxene-bearing crystal cumulate from the melt is essential to form the charnockites, and that the biotite granite forms from the evolved melt after the fractionation. The charnockite-biotite granite association of the studied area was formed in an extensional tectonic setting, presumably during the breakdown of the Columbia Supercontinent.

Identifying the genesis of hydrothermal activities in the Xiangcheng fault belt, southwestern China: Evidence from hydrochemistry and stable isotopes

Regional faults are beneficial structures for the formation of hydrothermal activities and have thus become target areas for geothermal resource utilization. Numerous hydrothermal activities have been reported along the Xiangcheng fault belt, particularly concentrating in the Batang, Xiangcheng and Shangri-La areas. In this study, hydrochemistry and stable isotopes were used to identify the genesis of hydrothermal activities in the Xiangcheng fault belt. The pH values of the geothermal water in these regions gradually decreases in this order, while the total dissolved solids gradually increase. The δD and δ18O values indicate the geothermal waters are mainly originated from snowmelt water and meteoric water. The recharge elevation of geothermal waters in Batang, Xiangcheng, and Shangri-La was 4415–4904 m, 4585–5038 m, and 3673–3969 m, respectively. Most geothermal waters belong to the hydrochemical type HCO3-Na, however some Batang geothermal water is of the SO4·HCO3-Na type, influenced by deep geothermal gas, and some Shangri-La geothermal water is of HCO3-Ca·Na type, influenced by shallow cold water and dissolution of carbonate rocks. Correlations of major ions suggest that HCO3-Na type geothermal waters are determined by the dissolution of paragonite, K-feldspar and albite as well as positive ion exchange. According to Na-K-Mg triangle diagram and mineral saturation indices, the geothermal waters do not reach full equilibrium and are mixed with shallow cold. Geothermometers, including cationic and SiO2, and geochemical thermodynamic calculations indicate that the deep and shallow reservoir temperatures are 200–240 °C and 169–193 °C for the Batang area, 194–201 °C and 119–131 °C for the Xiangcheng area, and 156–178 °C and 100–109 °C for the Shangri-La area. Conceptual models of the genesis of hydrothermal activities in the Batang, Xiangcheng, and Shangri-La areas were constructed, respectively. CaCO3 scaling is dominated in the study area. The hydrothermal activities of Batang and Xiangcheng areas with enriched deep materials and high reservoir temperatures are beneficial for rare-alkali metal (e.g., Li). The findings of this study provide a scientific basis for the development and utilization of geothermal resources in the high-temperature hydrothermal activity areas of western Sichuan.

Calcium single atoms stabilized by nitrogen coordination in metal–organic frameworks as efficient solid base catalysts

Considerable attention has been paid to the preparation of single-atom solid base catalysts (SASBCs) owing to their high activity and maximized utilization of basic sites. At present, the reported fabrication methods of SASBCs, such as two-step reduction strategy and sublimation capture strategy, require high temperature. Such a high activation temperature is easy to cause the sublimation loss of alkali or alkaline earth metal atoms and destructive to the support structure. Herein, a new SASBC, Ca1/UiO-67-BPY, is fabricated, in which the alkaline earth metal Ca sites are immobilized onto N-rich metal–organic framework UiO-67-BPY at room temperature. The results show that the atomic configuration of Ca single atoms is coordinated by two N atoms in the framework. The obtained Ca SASBC possesses ordered structure and exhibits high product yield of 87.2% in the Knoevenagel reaction between benzaldehyde and malononitrile. Furthermore, thanks to the Ca single atoms sites anchored on UiO-67-BPY, the Ca1/UiO-67-BPY catalyst also shows good stability during cycles. This work might offer new insight in designing SASBCs for different base-catalyzed reactions.

Luffa vines-derived N, O doped porous carbon with high surface area for supercapacitors

Considerable attention has been devoted to creating porous carbons with exceptional surface area and porosity from biomass waste for energy storage devices. Herein, we employed a straightforward high-temperature carbonization and KOH activation method to synthesize nitrogen (N) and oxygen (O) co-doped porous activated carbons derived from luffa vines (LVACs). The impact of varying KOH concentrations on the morphology, structure, and electrochemical properties of LVACs was thoroughly investigated. The optimal mass ratio of KOH to LVACs at 1:6 achieved the maximum specific surface area of 3369 m2 g−1. At a current density of 1 A g−1, the LASC-6 electrode exhibits an impressive specific capacitance of 348.5 F g−1. It also demonstrates exceptional rate performance, retaining 70.6 % of its capacitance at a current density of 20 A g−1. The electrode possesses robust cycling stability, retaining 90 % of the initial capacitance after 5000 cycles. We assessed the practicality of LVAC-6 by constructing symmetric supercapacitors (SSCs) using KOH and [BMIM]BF4 electrolytes. The KOH and [BMIM]BF4 SSCs achieved specific capacitances of 86.75 and 50.31 F g−1, respectively, at a current density of 0.25 A g−1. Moreover, the [BMIM]BF4 SSC exhibited an impressive energy density of 51.05 Wh kg−1 at a power density of 346.15 W kg−1. Therefore, we propose a simple and cost-effective strategy to produce porous carbon materials with excellent electrochemical performance from discarded biomass waste, facilitating the preparation of environmentally friendly electrode materials for high-performance supercapacitors.

Low-energy thermo-chemical conversion processes of municipal wet waste

Hydrothermal carbonization (HTC) is a low-energy thermochemical process that converts wet biomass into a carbon-rich solid, commonly called hydrochar, for use in a variety of areas, such as soil amendment, biofuels or to produce carbon-based materials. The purpose of this paper is to increase knowledge for the economic valorization of municipal wet waste, considered as a raw material to obtain high value-added products through an HTC process and an additional chemical activation procedure. In the first part of the work, a 4.5-liter batch reactor was designed, built, and used in the HTC experimental campaign by varying the main process parameters, namely reaction time, amount and type of organic waste (e.g. vegetables, fruits, bread, pasta), water concentration, temperature and pressure. In addition, some experiments were conducted by applying the steam explosion technique at the end of the HTC process. The HTC results showed that in biomass with high water content, increasing residence time decreases the hydrochar yield. Considering a dry heterogeneous waste with high carbon content, the yields at the end of the process are much higher. In the second part of this work, the hydrochar samples were treated with a high-temperature activation process based on the use of KOH, obtaining activated carbon. Particularly, the best results were achieved by using high KOH: hydrochar ratios, resulting in high-quality activated carbons with good porosity and a high surface area of 2890 m2/g. Finally, an energy analysis was carried out to evaluate how to make the whole process cost-effective.

Improving the NH3 oxidation and removing NOx during ammonia-rich fuel catalytic combustion using the Ag/CuOx@SiO2 catalyst with high-temperature catalytic activity

Ammonia, as a carbon-free, hydrogen-rich and renewable fuel, is of great significance for building the zero-carbon emission energy supply system in the word. However, the drawbacks of high ignition energy and high NOx emissions limit its widespread application. Catalytic combustion provides a reliable option for NH3 combustion. In the study, the catalyst of Ag/CuOx@SiO2 catalyst with high-temperature catalytic activity was prepared, and the catalytic flow reactor was employed to evaluate the ability of the catalyst in enhancing NH3 oxidation and removal NOx during NH3-rich combustion with high temperature region (900 K∼1400 K) and wide equivalence ratio range (0.4 ∼ 1.2). The high-temperature catalytic activity of the catalyst was proved by XPS spectrogram that the valence states of Ag and CuOx species in the catalyst have not been changed after the catalytic combustion. The results of catalytic combustion indicated that the catalyst enhanced the NH3 oxidation significantly. Compared to NH3 combustion, the temperature of 100 %NH3 conversion (T100) was decreased by over 500 K during NH3 catalytic combustion. Moreover, catalytic combustion performed higher efficiency on enhancing NH3 oxidation than the approach of co-firing NH3 with higher reactive gas fuels. The T100 of NH3 catalytic combustion was lower by 200 K∼220 K than that of NH3/H2 and NH3/CH4 combustion. Furthermore, the catalyst reduced the NOx effectively during NH3/H2 and NH3/CH4 combustion. At 1400 K, NO selectivity during NH3/H2 and NH3/CH4 catalytic combustion reduced by 86.80 %∼90.42 % and 43.61 %∼61.42 % compared to the combustion, respectively. Additionally, the peak of N2O selectivity moved to lower temperature range during catalytic combustion. Especially in stoichiometric and fuel rich conditions, the peak temperature reduced by 100 K∼200 K. The study provided references for the development of catalysts in ammonia-rich fuel catalytic combustion.

Promoting metal oxides–zeolite electron interaction on MnCeOx/HY catalyst for boosting nitrogen oxides reduction

The MnOx-CeO2 metal oxides are considered as promising alternative catalysts for selective catalytic reduction with NH3 (NH3-SCR) to remove NOx due to its excellent low temperature performance. However, their strong oxidative ability can lead to NH3 over-oxidation, narrowing the active temperature range and reducing N2 selectivity. Moreover, their weak surface acidity hampers medium to high-temperature activity and alkali metal resistance. Hence, in this study, MnCeOx metal oxides were coupled with HY zeolite to create MnCeOx/HY, demonstrating excellent NH3-SCR performance. The high dispersion of metal oxides on the zeolite surface and their close integration promoted strong electron interaction, effectively reducing oxygen vacancies and surface adsorbed oxygen concentrations. Consequently, the oxidative ability of active metal oxides was appropriately weakened, suppressing undesirable side reactions. MnCeOx/HY also notably suppressed NO adsorption and nitrate formation, promoting the catalytic reaction solely through the E-R mechanism and enhancing N2 selectivity. The abundant strong acid sites on the zeolite surface facilitates NH3 adsorption at moderate to high temperatures, notably expanding the active temperature window. Furthermore, the acid sites of HY zeolite serve as sacrificial sites, preferentially reacting with alkali metals, thus exhibiting excellent resistance to alkali metal poisoning on MnCeOx/HY. Combining with the DFT results, the structure-activity relationships in this study also reveal the importance of the effective synergy between acid sites and redox sites for optimal catalytic performance, offering valuable insights into the development of highly active and alkali-resistant denitrification catalysts.

A novel lytic phage infecting MDR Salmonella enterica and its application as effective food biocontrol.

Salmonella enterica is a foodborne pathogen associated with both typhoid and non-typhoid illness in humans and animals. This problem is further exacerbated by the emergence of antibiotic-resistant strains of Salmonella enterica. Therefore, to meet public health and safety, there is a need for an alternative strategy to tackle antibiotic-resistant bacteria. Bacteriophages or (bacterial viruses), due to their specificity, self-dosing, and antibiofilm activity, serve as a better approach to fighting against drug-resistant bacteria. In the current study, a broad-host range lytic phage phiSalP219 was isolated against multidrug-resistant Salmonella enterica serotypes Paratyphi from a pond water sample. Salmonella phage phiSalP219 was able to lyse 28/30 tested strains of Salmonella enterica. Salmonella phage phiSalP219 exhibits activity in acidic environments (pH3) and high temperatures (70°C). Electron microscopy and genome analysis revealed that phage phiSalP219 is a member of class Caudoviricetes. The genome of Salmonella phage phiSalP219 is 146Kb in size with 44.5% GC content. A total of 250 Coding Sequence (CDS) and 25 tRNAs were predicted in its genome. Predicted open reading frames (ORFs) were divided into five groups based on their annotation results: (1) nucleotide metabolism, (2) DNA replication and transcription, (3) structural proteins, (4) lysis protein, and (5) other proteins. The absence of lysogeny-related genes in their genome indicates that Salmonella phage phiSalP219 is lytic in nature. Phage phiSalP219 was also found to be microbiologically safe (due to the absence of toxin or virulence-related genes) in the control of Salmonella enterica serovar Typhimurium infections in the ready-to-eat meat and also able to eradicate biofilm formed by the same bacterium on the borosilicate glass surface.

Evaluation of hydrogen storage performance of Ti0.25Zr0.25V0.15Nb0.15Ta0.2 high-entropy alloy using calorimetric technique

The features of phase transformations during interaction of BCC-type Ti0.25Zr0.25V0.15Nb0.15Ta0.2 high-entropy alloy (HEA) with hydrogen and the accompanying thermal effects have been examined using the Tian-Calvet calorimetric technique. The alloy was produced by the pendent drop melt extraction method in the form of microfibers and then coated with a thin layer of palladium to eliminate the preliminary high-temperature activation and enable first hydrogenation at room temperature. Two reaction stages were distinguished on the measured heat emission curves. Using XRD data, these stages were attributed to the formation of a BCC-type hydrogen solid solution and a phase transition to FCC-type dihydride phase. Recorded values of the reaction enthalpy decrease in absolute terms from 145 kJ/mol H2 (dilute solid solution) to 73–77 kJ/mol H2 (BCC→FCC) and to 20 kJ/mol H2 (H solution in FCC dihydride). The overall heat emission of the entire process as a whole is 110 kJ/ mol H2. The course of the dehydrogenation process depends strongly on the applied temperature and at 493 K results in the formation of a BCT-type monohydride, which was not detected during hydrogenation. The detailed calorimetric data obtained here significantly change the previously existing ideas about thermal effects during this type HEAs hydrogenation, based on calculations using the Van't-Hoff equation. The reported findings are of special importance for various hydrogen related applications of HEAs

Quantifying the Hydration-Dependent Dynamics of Copper Migration and Activity in Zeolite Omega for the Partial Oxidation of Methane.

Copper-exchanged zeolite omega (Cu-omega) is a potent material for the selective conversion of methane-to-methanol (MtM) via the oxygen looping approach. However, its performance exhibits substantial variation depending on the operational conditions. Under an isothermal temperature regime, Cu-omega demonstrates subdued activity below 230 °C, but experiences a remarkable increase in activity at 290 °C. Applying a high-temperature activation protocol at 450 °C causes a rapid deactivation of the material. This behavioral divergence is investigated by combining reactivity studies, neutron and in situ high-resolution anomalous X-ray powder diffraction (HR-AXRPD), as well as electron paramagnetic resonance spectroscopy, to reveal that the migration of Cu throughout the framework is the primary cause of these behaviors, which in turn is governed by the degree of hydration of the system. This work suggests that control over the Cu migration throughout the zeolite framework may be harnessed to significantly increase the activity of Cu-omega by generating more active sites for the MtM conversion. These results underscore the power of in situ HR-AXRPD for unraveling the behavior of materials under reaction conditions and suggest that a re-evaluation of Cu-zeolites priorly deemed inactive for the MtM conversion across a broader range of conditions and looping protocols may be warranted.

Performance study of high energy storage supercapacitor from waste corn husk biomass electrode materials

Waste biomass carbon materials are used as green and environmentally friendly electrode materials for supercapacitors (SCs) have great development prospects, therefore, miscellaneous elements-rich and recycled renewable porous carbon materials have important applications value in the field of energy storage device. In this paper, waste corn husk as biomass precursor to prepare corn husk porous carbon (CHPC) using two steps of high-temperature carbonization and KOH activation. The CHPC-2 optimized by KOH shows a specific surface area (SSA) of 1103 m2 g−1 and a total pore volume of 0.83 cm3 g−1, achieving a high specific capacitance of 413.4 F g−1 at 0.5 A g−1. After 10,000 cycles, only 4.17 % of the capacitance was lost. In a two-electrode system with 1 M Na2SO4 as the electrolyte, CHPC-2//CHPC-2 exhibits a specific capacitance of 333 F g−1 at a wide voltage window of 0–1.8 V, and energy density of 37.46 Wh Kg−1 when power density is 450 W kg−1, which possesses the capacitance retention rate of 85.16 % after 5000 cycles. The assembled symmetrical SCs contain capacitance of 308.79 F g−1, and 21.02 Wh kg−1 under a power density of 350 W kg−1 in PVA/KOH gel electrolyte. Consequently, CHPC materials provide a scientific and reasonable research idea for the development of SCs with inexpensive, non-polluting, and high energy density.