Magnesium Acetate Research Articles

Salvianolate injection ameliorates cardiomyopathy by regulating autophagic flux through miR-30a/becn1 axis in zebrafish.

Salvianolate is a compound mainly composed of salvia magnesium acetate, which is extracted from the Chinese herb Salvia miltiorrhiza. In recent years, salvianolate injection has been widely used in the treatment of cardiovascular diseases, but the mechanism of how it can alleviate cardiotoxicity remains unclear. The cardiac injury model was constructed by treatment with doxorubicin (Dox) or azithromycin (Azi) in zebrafish larvae. Heart phenotype, heart rate, and cardiomyocyte apoptosis were observed in the study. RNA-seq analysis was used to explore the underlying mechanism of salvianolate treatment. Moreover, cardiomyocyte autophagy was assessed by in situ imaging. In addition, the miR-30a/becn1 axis regulation by salvianolate was further investigated. Salvianolate treatment reduced the proportion of pericardial edema, recovered heart rate, and inhibited cardiomyocyte apoptosis in Dox/Azi-administered zebrafish larvae. Mechanistically, salvianolate regulated the lysosomal pathway and promoted autophagic flux in zebrafish cardiomyocytes. The expression level of becn1 was increased in Dox-induced myocardial tissue injury after salvianolate administration; overexpression of becn1 in cardiomyocytes alleviated the Dox/Azi-induced cardiac injury and promoted autophagic flux in cardiomyocytes, while becn1 knockdown blocked the effects of salvianolate. In addition, miR-30a, negatively regulated by salvianolate, partially inhibited the cardiac amelioration of salvianolate by targeting becn1directly. This study has proved that salvianolate reduces cardiomyopathy by regulating autophagic flux through the miR-30a/becn1 axis in zebrafish and is a potential drug for adjunctive Dox/Azi therapy.

Solvent-free mechanochemical synthesis of Mg-gallic acid complex for the fabrication of high-performance supercapacitor porous carbon

At molecular level, it is challenging to construct a porous carbon from magnesium based template and low cost precursor by a facile route for supercapacitive energy storage, e.g. solvent-free approach because the coordination of magnesium ion with organic ligands usually needs participation of solvent. Herein, a balling milling mediated coordination of magnesium acetate and gallic acid was developed in the absence of solvent to prepare porous carbon. The key of the present strategy lies in the generation of volatile HAc, orienting the reaction in a favorable direction for the formation of complexes. The resultant porous carbon (denoted BGMC) owns a high microporostiy ratio (24.2 % vs template-free derived ones of 11.1 %), open accessed microstructure and hydrophobic character. As electrode for supercapacitor, in aqueous electrolyte, the BGMC based supercapacitor achieves a high energy density of 19.2 Wh kg−1@900 W kg−1, while, in organic electrolyte of 1.0 M TEABF4/AN, the symmetric device based on BGMC delivers energy in a wide voltage window of 0–3.5 V with large energy of 34.4 Wh kg−1@1750 W kg−1, which is superior to those of recently reported carbon based devices. And more, at high current density of 10 A g−1, the BGMC device can resist continual charge/discharge for 30 000 cycles, showing an excellent cycling stability. Our strategy involving solvent-freely coordination of template and precursor molecule to prepare porous carbon open up a route with facile, scalable and easy-operable attributes towards the preparation of functional porous carbon.

An Optimized CRISPR/Cas12a Assay to Facilitate the BRAF V600E Mutation Detection.

Accurate detection of the BRAF V600E (1799T > A) mutation status can significantly contribute to selecting an optimal therapeutic strategy for diverse cancer types. CRISPR-based diagnostic platforms exhibit simple programming, cost-effectiveness, high sensitivity, and high specificity in detecting target sequences. The goal of this study is to develop a simple BRAF V600E mutation detection method. We combined the CRISPR/Cas12a system with recombinase polymerase amplification (RPA). Subsequently, several parameters related to CRISPR/Cas12a reaction efficiency were evaluated. Then, we conducted a comparative analysis of three distinct approaches toward identifying BRAF V600E mutations in the clinical samples. Our data suggest that CRISPR/Cas detection is considerably responsive to variations in buffer conditions. Magnesium acetate (MgOAc) demonstrated superior performance compared to all other examined additive salts. It was observed using 150 nM guide RNA (gRNA) in an optimized reaction buffer containing 14 mM MgOAc, coupled with a reduction in the volumes of PCR and RPA products to 1 μL and 3 μL, respectively, resulted in an enhanced sensitivity. Detection time was decreased to 75 min with a 2% limit of detection (LOD), as evidenced by the results obtained from the blue light illuminator. The CRISPR/Cas12a assay confirmed the real-time PCR results in 31 of 32 clinical samples to identify the BRAF V600E mutation status, while Sanger sequencing detected BRAF V600E mutations with lower sensitivity. We propose a potential diagnostic approach that is facile, fast, and affordable with high fidelity. This method can detect BRAF V600E mutation with a 2% LOD without the need for a thermocycler.

LDH@MgSiO3 multi-core@shell catalyst for dry reforming of methane

In this paper, LDH@SiO2 catalyst was prepared via coating a layer of silica over LDH (Layered Double Hydroxide) nanoplates. Then it was calcined and further treated by hydrothermal method with magnesium acetate to convert silica layer into MgSiO3. After H2- reduction, a layer of branch-like MgSiO3 was observed as the shell and nickel nanoparticles with average diameter around 10 nm were encapsulated within the shell, which was called as LDH@MgSiO3 multi-core@shell catalyst. This catalyst was then tested in dry reforming of methane (DRM) at 675 °C and the CH4 conversion was kept stable around 25% for 30 h time on stream at GHSV of 360 L/gcat/h. Besides, the H2/CO ratio in the product gas was 0.85, much higher than that of LDH@SiO2 catalyst, indicating its superb selectivity. Characterization revealed that the formation of MgSiO3 was beneficial to reduce the nickel particle size, modify the porosity and improve the surface alkalinity, which enhanced the DRM activity and selectivity. More importantly, it enhanced the hydrothermal stability, thus preventing the reconstruction of the shell.

Untargeted metabolomics reveals the mechanism for leaching rare earth elements from ion-adsorption rare earth ores using a composite lixiviant

Rare earth elements (REEs) are an important strategic scarce resource, and how to mine and utilise them efficiently and greenly is a difficult problem. In this study, to reduce the use of chemical reagents in the leaching process, Bacillus thuringiensis fermentation broth and magnesium acetate were used as composite lixiviants to leach REEs from ionic rare earth ores via biochemical synergy. The effectiveness of composite lixiviant for leaching REEs was studied, and the optimum leaching conditions were determined. In addition, untargeted metabolomics was used to explore metabolite differences and metabolic pathway profiles before and after leaching with the composite lixiviant. The interaction between the composite lixiviant and the rare earth minerals was also investigated by combining various characterisation tools. The results showed that the leaching rate was 96.3 % when the concentration of magnesium acetate in the composite lixiviant was 0.3 mol/L, the pH was 4, and the liquid–solid ratio was 2:1. Metabolomics analysis showed that lipids and lipid-like molecules, benzenoids, and organic acids, and derivatives contained in the fermentation broth of the complex leach play an important role in the leaching process. This study provides a new composite lixiviant for leaching ionic REEs, which can reduce the dosage of chemical reagents, provide a reference for the biochemical synergistic leaching of ionic rare earth ores, and help guide environmentally friendly and efficient leaching of ionic rare earth ores in the future.

The first example of a polyhedral boron derivative of gadolinium(III) phthalocyaninate as a promising prototype of a theranostic agent

We report the first synthesis of a polyhedral boron derivative of gadolinium(III) phthalocyaninate. Initially, reaction of 4-nitrophthalonitrile with 4-formylphenol in the presence of base was carried out to give 4-(4-formylphenoxy)phthalonitrile. This compound was then converted to 4-(4-hydroxymethylphenoxy)phthalonitrile using sodium tris-acetoxy borohydride in THF. Sequential cyclotetramerisation of this semiproduct in the presence of magnesium acetate, treatment of the resulting complex with trifluoroacetic acid, and complexation with gadolinium(III) acetate afforded gadolinium(III) phthalocyanine containing four hydroxymethylphenoxy groups at the peripheral (β) positions. Then, a nucleophilic addition reaction of this complex with acetonitrilium derivative of [B10H10]2- anion afforded gadolinium(III) phthalocyaninate decorated with four closo-decaborate units in good/satisfactory yield. The new product was characterised by various techniques (CHN analysis, MALDI-TOF mass spectrometry and UV–Vis spectroscopy). The boron content in this product is 21.5 wt% (40 atoms), and the r1 relaxivity of the conjugate 6.1 ± 0.7 mM-1s−1 (at 3.0 T, 20 °C in water), which makes it a promising prototype for theranostic agents for MRI-guided BNC therapy in future investigations.

Novel promising aqueous electrolytes for manganese dioxide/stainless steel pseudocapacitor electrode

Manganese dioxide (MnO2) films are developed by potentiostatic electrodeposition on a stainless steel sheet as a current collector using manganese acetate tetrahydrate solution at a concentration of 0.25 mol L−1. The deposited sample layer is found to be amorphous as confirmed by the scanning electron microscope (SEM) and X-ray diffraction (XRD) analyses. The capacitive property of the prepared electrodes is characterized by charging/discharging, cyclic voltammetry, and electrochemical impedance spectroscopy techniques in four different aqueous solutions; sodium sulfate, magnesium acetate, nickel acetate, and a mixture of sodium chloride + sodium bicarbonate + borax. Charge–discharge curves reveal higher specific capacitance (Cs) of 1580 F g−1 at 0.5 mA cm−2 for the investigated MnO2 film which is characterized in Ni acetate aqueous solution. The structural, morphological, and electrochemical properties of the electrodeposited manganese oxide films are also studied. The results indicate that the specific capacitance of the deposited samples showed a strong dependency on the electrolyte aqueous solutions, resulting in developing new electrolytes which is a top priority effort in comparison to seeking new electrode materials. It is found that the matching between the pore size structure of the electrode and the ion size of the electrolyte is of great importance for the improved capacity of prepared capacitors.

Unlocking precision: Advancing rapid field molecular identification of Tuta absoluta across its life cycle using locked nucleic acid strategies

Rapid and accurate insect identification is crucial for effective plant quarantine procedures. This study introduced a reverse transcription recombinase-assisted amplification-lateral flow strip (RT RAA-LFS), specifically designed for on-site detection of the globally quarantined pest, Tuta absoluta, within a 25-minute timeframe. A pivotal strategy involved integrating three locked nucleic acid (LNA) modifications into a species-specific probe, enabling RT RAA to selectively and efficiently amplify the unique haplotype of T. absoluta's mitochondrial cytochrome c oxidase subunit I (COI) gene. After determining the amplification product dilution factor and the volumes of primers, magnesium acetate, and nucleic acid lysate in the amplification system, the finalized RT RAA-LFS system is capable of direct visual detection, complemented by handheld fluorescence detection for quantum dots (QDs) fluorescence on the lateral flow strip. This technique successfully identifies various developmental stages of T. absoluta in crude nucleic acid lysates without the need for genomic DNA extraction. Moreover, it detected the target gene in the genomic solution, reaching concentrations as low as 1.6 pg or 51 copies per 50-µL reaction system, aligning with qPCR results. Field validation with 50 insect samples supports the correlation between RT RAA-LFS quantum dots' fluorescence intensity and LFS color intensity, affirming the system's reliability in estimating the target gene copy number (R=0.584, p < 0.01). This validation emphasizes the practical efficacy of the RT RAA-LFS system for T. absoluta detection, highlighting its potential as a rapid on-site tool in agricultural pest management.

Multi-scale measurement of constitutive viscoelastic properties of bituminous composites considering moisture and deicing conditions

The use of salt and chemical deicers can cause significant damage to road infrastructures. This study investigates the impact of different deicers on the viscoelastic properties of mastic and asphalt mixtures, with a focus on characterizing their behavior at varying temperatures and loading frequencies. The samples were subjected to conditioning in solutions of distilled water, salt, Calcium Magnesium Acetate (CMA), and Potassium Acetate (KAc) at 60 °C for 96 h, followed by frequency sweep and dynamic modulus tests at different temperatures and loading frequencies. The results indicate that moisture conditioning with distilled water softens asphalt mixtures and mastic at low loading frequencies, while brine softens the former at low temperatures. Salt's high interaction with mixture aggregates cannot be ignored. CMA's effect on the fatigue behavior of mastic samples is highly dependent on loading frequency, while KAc increases stiffness at intermediate and high temperatures. All the deicers reduce resistance to rutting damage, with CMA having the most negative effect. Both the 2S2P1D and the generalized Maxwell model can well (R2 ≥ 0.90, Se/Sy ≤ 0.35) predict the viscoelastic properties of dry asphalt mixture. However, in the presence of distilled water and the deicers, asphalt mixture viscoelastic properties cannot be predicted according to asphalt mastic characteristics by implementing the homothety method which indicates different effects of distilled water and the deicers on various scales of bituminous composites.

Synthesis, Structural, and Optical Properties of 2-(2-methyl 8-hydroxyquinoline) Magnesium Nanorods for Optical Display Systems.

Organic semiconductors find widespread applications in the realm of organic light-emitting diodes (OLEDs) as well as organic photovoltaic cells. In the domain of OLED devices, it is plausible for nano-based Mg metal complexes to play a role as electron and hole-transport layers. In the present investigation, we synthesized 2(2-methyl 8-hydroxyquinoline) magnesium [Mg(mq)2] nanorods through the employment of the precipitation method, using 2-methyl 8- hydroxyquinoline and magnesium acetate. We employed various techniques to characterize the Mg(mq)2 nanorods, including powder XRD, FTIR spectroscopy, SEM, EDX, UV-Vis, and PL spectroscopy studies. The structural aspects of Mg(mq)2 were ascertained through P-XRD analysis. The elemental composition of Mg(mq)2 and its surface texture were established via EDX and HR-SEM analyses. FTIR spectroscopy confirmed the existence of functional groups within the sample. UV-Vis spectroscopy was utilized to evaluate the optical absorbance, bandgap, and Urbach energy of Mg(mq)2. The luminescence properties of the Mg(mq)2 nanorods were determined from the photoluminescence study. The characterization results were compared with the Zn(mq)2 nano samples. The experimental results presented herein serve to demonstrate the practicality of employing Mg(mq)2 nanorods in OLED devices.

Low core loss and high DC bias performance of FeSiAl soft magnetic composites cores with hybrid insulating layers of MgO/SiO2

Soft magnetic composites (SMCs) play an indispensable role in electromagnetic conversion, transmission, and storage. However, in order to achieve miniaturization, energy conservation, and meet the application requirements of premagnetisation in direct-current (DC) components, SMCs are required to have low core loss and high DC bias performance. In this work, FeSiAl SMCs with hybrid insulating layers of MgO/SiO2 have been successfully prepared by the decomposition of magnesium acetate tetrahydrate and silicone resin. The presence of MgO and SiO2 insulating layers can effectively compensate for each other's coating defects, thereby forming complete insulating layers on the surface of FeSiAl powders to reduce the core loss. Finally, the FeSiAl@MgO/SiO2 SMC gets remarkable comprehensive magnetic properties with a low core loss (Pcv) of 163.7 mW/cm3 at 50 mT/100 kHz, a high DC bias performance of 53.7 % at 100 Oe, and an effective permeability (μe) of 46, which is promising for high-frequency and high-power applications.

Wide band gap tuning of Mg doped ZnO thin films for optoelectronic applications.

Zinc oxide (ZnO) thin films with magnesium (Mg) doping have demonstrated significant potential due to their wide band gap, which enables efficient absorption of ultraviolet (UV) radiation while maintaining transparency to visible light. Sol-gel spin coating methods were used to deposit Mg-doped ZnO thin films. The solution was made with methanol as the solvent, and the starting materials were magnesium acetate tetrahydrate and zinc acetate dihydrate. The integration of Mg content in deposited ZnO films was investigated for structural, morphological, and optical properties using an X-ray diffractometer (XRD), scanning electron microscope (SEM), energy dispersive X-ray analysis (EDAX), and UV-VIS spectrophotometer. Mg-doped ZnO films were produced on quartz substrates and post-annealed at 400°C. According to absorption coefficient calculations, the optical band gap of Mg-doped ZnO films is in the range of 5.4 eV which is ideal for a variety of applications in the field of optoelectronic devices.

The postbiotic sodium butyrate synergizes the antiproliferative effects of dexamethasone against the AGS gastric adenocarcinoma cells.

A growing body of literature underlines the fundamental role of gut microbiota in the occurrence, treatment, and prognosis of cancer. In particular, the activity of gut microbial metabolites (also known as postbiotics) against different cancer types has been recently reported in several studies. However, their in-depth molecular mechanisms of action and potential interactions with standard chemotherapeutic drugs remain to be fully understood. This research investigates the antiproliferative activities of postbiotics- short-chain fatty acid (SCFA) salts, specifically magnesium acetate (MgA), sodium propionate (NaP), and sodium butyrate (NaB), against the AGS gastric adenocarcinoma cells. Furthermore, the potential synergistic interactions between the most active SCFA salt-NaB and the standard drug dexamethasone (Dex) were explored using the combination index model. The molecular mechanisms of the synergy were investigated using reactive oxygen species (ROS), flow cytometry and biochemometric and liquid chromatography-mass spectrometry (LC-MS)-driven proteomics analyses. NaB exhibited the most significant inhibitory effect (p < 0.05) among the tested SCFA salts against the AGS gastric cancer cells. Additionally, Dex and NaB exhibited strong synergy at a 2:8 ratio (40 μg/mL Dex + 2,400 μg/mL NaB) with significantly greater inhibitory activity (p < 0.05) compared to the mono treatments against the AGS gastric cancer cells. MgA and NaP reduced ROS production, while NaB exhibited pro-oxidative properties. Dex displayed antioxidative effects, and the combination of Dex and NaB (2,8) demonstrated a unique pattern, potentially counteracting the pro-oxidative effects of NaB, highlighting an interaction. Dex and NaB individually and in combination (Dex:NaB 40:2400 μg/mL) induced significant changes in cell populations, suggesting a shift toward apoptosis (p < 0.0001). Analysis of dysregulated proteins in the AGS cells treated with the synergistic combination revealed notable downregulation of the oncogene TNS4, suggesting a potential mechanism for the observed antiproliferative effects. These findings propose the potential implementation of NaB as an adjuvant therapy with Dex. Further investigations into additional combination therapies, in-depth studies of the molecular mechanisms, and in vivo research will provide deeper insights into the use of these postbiotics in cancer, particularly in gastric malignancies.

N-doped hierarchically porous carbons prepared with the assistance of chemical blowing and in-situ hard template as highly efficient CO2 adsorbents: A combined experimental and theoretical study

In the current work, we presented the synthesis of N-doped hierarchically porous carbons (NDHPCs) through chemical activation of hierarchically structured precursor derived from polyvinylpyrrolidone (PVP) and magnesium acetate tetrahydrate. Magnesium acetate tetrahydrate served as the blowing agent, and its decomposition product MgO served as the in-situ formed hard template. Combined with KHCO3 activation, the NDHPCs demonstrated a unique micro-meso-macroporous structure. Owing to the highly porous structure (1560–2545 m2/g) and enriched N-doping (1.48–6.31 wt%), the NDHPCs were investigated as potential CO2 adsorbents in both post-combustion capture and pre-combustion capture applications. When the adsorption temperature was 25 °C, the samples showed outstanding capture performances at both 1 bar (2.97–3.88 mmol/g) and 20 bar (13.24–19.89 mmol/g). The adsorption performances were further analyzed with grand canonical Monte Carlo (GCMC) simulation. Effects of various physicochemical properties on CO2 adsorption at different pressures were thus revealed with a combined experimental-theoretical approach.

Evaluation of the technical properties of reactive-MgO cements produced by solar calcination of magnesite in a fluidized bed reactor

Magnesium oxide (MgO)-based cements display very interesting technical properties and environmentally-friendly features. The novel idea investigated in this study is to synthesize MgO cements, using as raw material natural magnesite calcined in fluidized bed heated by concentrated solar energy. Calcination was performed in a lab-scale system equipped with a concentrated solar simulator, operated under different process conditions. The most reactive MgO was mixed with 3% by weight of MgCO3 (nucleation agent) and four different solutions containing magnesium acetate or chloride. The binders were hydrated in air or 20% CO2 atmosphere (accelerated carbonation conditions) until 28 days. X-ray diffraction, differential-thermal and mercury intrusion porosimetry analyses, and compressive mechanical strength tests, were performed on the hydrated systems. Solar calcination produced a highly reactive MgO. The performance of the cement pastes improved at higher curing times, and when using magnesium acetate as hydration agent, as also witnessed by the application of a kinetic model. Accelerated carbonation conditions further enhanced the mechanical properties of the cements thanks to the formation of nesquehonite, allowing to reach a mechanical strength comparable to that of ordinary Portland cements class 32.5. The achieved outcomes encourage the production of low-CO2 magnesite cements from solar calcined magnesite, boosting the green aspect of the entire process.

The Treatment of Natural Calcium Materials Using the Supercritical Antisolvent Method for CO2 Capture Applications

The potential of the supercritical antisolvent micronization (SAS) technique was evaluated for the production of CaO-based particles with a size and a physical structure that could enable high performance for CO2 capture through the calcium looping process. Two sources of calcium derivative compounds were tested, waste marble powder (WMP) and dolomite. The SAS micronization of the derivate calcium acetate was carried out at 60 °C, 200 bar, a 0.5 mL min−1 flow rate of liquid solution, and 20 mg mL−1 concentration of solute, producing, with a yield of more than 70%, needle-like particles. Moreover, since dolomite presents with a mixture of calcium and magnesium carbonates, the influence of the magnesium fraction in the SAS micronization was also assessed. The micronized mixtures with lower magnesium content (higher calcium fraction) presented needle-like particles similar to WMP. On the other hand, for the higher magnesium fractions, the micronized material was similar to magnesium acetate micronization, presenting sphere-like particles. The use of the micronized material in the Ca-looping processes, considering 10 carbonation-calcination cycles under mild and realistic conditions, showed that under mild conditions, the micronized WMP improved CaO conversion. After 10 cycles the micronization, WMP presented a conversion 1.8 times greater than the unprocessed material. The micronized dolomite, under both mild and real conditions, maintained more stable conversion after 10 cycles.

Silver Containing Antimicrobial Coatings on Innovative Ti-30Nb-5Mo β-Alloy Prepared by Micro-Arc Oxidation for Biomedical Implant Applications

Micro-arc oxidation (MAO) is a versatile surface-modification method that promotes higher wear and corrosion resistance, osseointegration, and biological activity to titanium alloys’ surfaces. This study aimed to modify the surface of a recently developed metastable β Ti alloy, which exhibits more favorable mechanical properties for implant applications compared to some commercial Ti alloys, by incorporating Ag into the coatings to introduce a bactericidal function to the surface. The Ti-30Nb-5Mo alloy, with lower elastic modulus, was treated by the MAO method using electrolyte solutions containing calcium acetate, magnesium acetate, β-glycerol phosphate, and varied concentrations of silver nitrate (1.5 mM, 2.5 mM, and 3.5 mM). With an increase in the concentration of silver ions in the electrolyte, the galvanostatic period during the MAO process decreased from 1.7 s to 0.5 s. The Ca/P ratio increased from 0.72 up to 1.36. X-ray diffraction showed that the MAO coatings were formed by rutile and anatase TiO2 main phases and calcium phosphates. X-ray photoelectron spectroscopy analysis detected the presence of amorphous Nb2O5, CaCO3, and MgCO3, and metallic and oxide forms of Ag. The increase in Ag in the electrolyte decreased the coating thickness (from 14.2 μm down to 10.0 μm), increased the contact angle (from 37.6° up to 57.4°), and slightly increased roughness (from 0.64 μm up to 0.79 μm). The maximum inhibition of Enterococcus faecalis, Pseudomonas aeruginosa, and Candida albicans strains growth was of 43%, 43%, and 61%, respectively. The Ag did not negatively affect the differentiation of adipose-tissue-derived mesenchymal stem cells. Therefore, the treatment of the surface of the innovative Ti-30Nb-5Mo alloy by the MAO method was effective in producing a noncytotoxic porous coating with bactericidal properties and improved osseointegration capabilities.

High-rate electrochimcal supercapacitor with attractive energy density assembling from infused-undaria-pinnatifida-based activated carbon

In order to achieve attractive energy density and specific capacitance of electrochemical supercapacitor, multi-heteroatom self-doped carbon is prepared by pyrolyzing the aquatic biomass undaria pinnatifida (UP) filled with magnesium acetate (Mg(CH3COO)2). The pyrolysis product of magnesium oxide (MgO), acting as rigid filling, can shape the pore and help to keep the original pore system. The resultant immersed-undaria-pinnatifida-based activated carbon (IUPAC-700) co-doped with multi-heteroatom shows specific surface area of 1116 m2 g−1, pore volume of 1.63 cm3 g−1 and desired pore size distribution. The electrode basing on it delivers specific capacitance of 579.7 F g−1 at the current density of 0.50 A g−1 and 306.0 F g−1 at 100.0 A g−1 in the electrolyte of 1.0 M H2SO4. It exhibits a high specific capacitance of 488.6 F g−1 in the two-electrode system and provides a significant energy density of 28.7 W kg−1 at the power density of 164.0 W kg−1. It also displays perfect cyclic life after 8000 times charge-discharge at the current density of 5.0 A g−1. The assembled supercapacitor can power the LED lights. The sample IUPAC-700 featured with self-doped multi-heteroatoms is a very competitive electrode material for energy storage device with desired comprehensive performance.

Microwave–assisted hydrothermal conversion of crop straw into value–added products via magnesium acetate

Rational utilization of crop straw is conducive to sustainable development of society. This study focused on the mechanism for the effect of magnesium acetate on the microwave–assisted hydrothermal conversion (MHTC) products of crop straw for more efficient use of resources. The results showed that magnesium acetate improves the hydrothermal liquid yield and quality of hydrochar from crop straw under MHTC. With increasing amount of magnesium acetate, there were obvious increases in TOC concentration and organic acid concentration, while notable decreases in total sugar concentration of hydrothermal liquid. Magnesium acetate promoted the conversion of nitrogen and phosphorus elements to inorganic forms and the release of potassium, calcium, and magnesium ions, leading to increases in both conductivity and pH value of the hydrothermal liquid. Furthermore, magnesium acetate promoted the hydrolysis of crop straw, facilitated the formation of carbon microspheres, and greatly increased the surface area, mesopore volume, and average diameter of hydrochar. With increasing addition amount of magnesium acetate, there was an increase in oxygen–containing groups in the hydrochar. The equilibrium moisture content of the hydrochar remained at high levels (54.09–61.30 wt%), with the maximum values ranging from 60.71 wt% to 61.30 wt%. Finally, the concentrations of acetate and magnesium ions were found to be two parameters with the highest correlation and contribution with the organic matter concentration in hydrothermal liquid and also the greatest influence on the physicochemical properties of hydrochar by affecting the hydrolysis process of crop straw.

Interaction of Magnesium Ion and Acetate Anion in Bulk Water: Toward High-Level Machine Learning Potential

Interaction of Magnesium Ion and Acetate Anion in Bulk Water: Toward High-Level Machine Learning Potential