High-carbon-content biochar from chemical manufacturing plant sludge for effective removal of ciprofloxacin from aqueous media.

Biochar is considered a promising biosorbent for harmful organic pollutants in aqueous media. However, only a limited number of biochars derived from industrial sludges have been utilized due to their problematic high ash content and heavy metal leaching. In this study, a highly effective biochar was prepared as a superabsorbent for ciprofloxacin (CIP) from chemical manufacturing plant sludge via K2CO3-activated pyrolysis, and its CIP removal behavior was evaluated. Unlike sewage sludge, chemical manufacturing plant sludge contains low SiO2, resulting in an ultra-pure carbon (95.4%) based biochar with almost negligible ash content. As the pyrolysis temperature increased from 400 to 800 °C, the ordered graphitic carbon structure transformed into an amorphous carbon phase, and most oxygen-containing groups disappeared. However, the pore size significantly decreased to ∼4.5 nm due to the corrosive carbon volatilization caused by K2CO3, resulting in an extremely large surface area of 2331.8 m2/g. Based on its large surface area and porous carbon structure, the activated biochar at 800 °C (CAB-800) exhibited an outstanding CIP adsorption capacity of 555.56 mg/g. The CIP adsorption isotherm, kinetic, and thermodynamic studies were systematically investigated. The CIP adsorption on CAB-800 was mainly attributed to π-π interactions and hydrogen bond formation, with electrostatic interactions partially contributing to the adsorption reaction. From pH 2 to 12, CAB-800 showed an excellent CIP adsorption capacity of over 316.7 mg/g, with adsorption favored under acidic conditions. Except for HCO3- and CO32-, the presence of anions and humic acids did not significantly affect CIP adsorption capacity. These results demonstrate that biochar produced from chemical manufacturing industry sludge via K2CO3 activation is a highly feasible material for the removal of CIP from aqueous media.

Synthesis and characterisation of K2CO3-activated carbon produced from distilled spent grains for the adsorption of CO2.

Activated carbon was prepared from distilled spent grains (DSG) using K2CO3 activation and chitosan modification. The effects of activator dosage, activation temperature, and the incorporation of chitosan as a nitrogen source on the adsorption performance were studied in this paper. The activated carbons were characterised by scanning electron microscopy, X-ray photoelectron spectroscopy, and nitrogen and carbon dioxide gas adsorption. Under the optimal conditions, the BET-specific surface area, total pore volume, and microporous volume of the activated carbon were as high as 1142 m2/g, 0.62 cm3/g, and 0.40 cm3/g, respectively. Chitosan was used as the nitrogen source, and surface modification was carried out concurrently with the K2CO3 activation process. The results revealed a carbon dioxide adsorption capacity of 5.2 mmol/g at 273.15 K and 1 bar without a nitrogen source, which increased to 5.76 mmol/g after chitosan modification. The isosteric heat of adsorption of CO2 all exceed 20 kJ/mol, hinting at the coexistence of both physisorption and chemisorption. The adsorption behaviour of the DSG-based activated carbon can be well-described by the Freundlich model.

Dynamic Intermediate-Temperature CO2 Adsorption Performance of K2CO3-Promoted Layered Double Hydroxide-Derived Adsorbents.

The dynamic adsorption characteristics of K2CO3-promoted layered double hydroxides (LDHs)-based adsorbent, with organic and inorganic anion intercalation, were studied. MgAl-LDH, K2CO3/MgAl-LDH, and K2CO3/MgAl-LDH(C16) with varying K2CO3 loads were prepared and used for intermediate-temperature CO2 sequestration. The adsorbent was thoroughly characterized using X-ray diffraction, Brunauer-Emmett-Teller, scanning electron microscopy, and Fourier Transform Infrared Spectroscopy techniques, which revealed enhanced adsorption properties of MgAl-LDH, due to K2CO3 promotion. Thermogravimetric CO2 adsorption tests on the constructed adsorbent materials showed that the 12.5 wt% K2CO3/MgAl-LDH(C16) adsorbent with organic anion intercalation exhibited optimal adsorption activity, achieving an adsorption capacity of 1.12 mmol/g at 100% CO2 and 350 °C. However, fixed-bed dynamic adsorption tests yielded different results; the 25 wt% K2CO3/MgAl-LDH prepared through inorganic anion intercalation exhibited the best adsorption performance in low-concentration CO2 penetration tests. The recorded penetration time was 93.1 s, accompanied by an adsorption capacity of 0.722 mmol/g. This can be attributed to the faster adsorption kinetics exhibited by the 25 wt% K2CO3/MgAl-LDH adsorbent during the early stages of adsorption, thereby facilitating efficient CO2 capture in low-concentration CO2 streams. This is a conclusion that differs from previous reports. Earlier reports indicated that LDHs with organic anion intercalation exhibited higher CO2 adsorption activity in thermogravimetric analyzer tests. However, this study found that for the fixed-bed dynamic adsorption process, K2CO3-modified inorganic anion-intercalated LDHs perform better, indicating their greater potential in practical applications.

Optimization of K2CO3 exposure conditions using response surface methodology for CO2 capture with 2-methylpiperazine and monoethanolamine as promoters.

In this study, the optimization of potassium carbonate (K2CO3) exposure conditions for CO2 capture with the use of 2-methypiperazine (2MPz) and monoethanolamine (MEA) as promoters was investigated. The tested operating conditions for the CO2 capture process included the pH, temperature, K2CO3 dose, gas flow rate, and pressure, and their effect on the CO2 absorption/desorption rate and CO2 absorption efficiency was assessed. Response surface methodology (RSM) was also employed to determine the equations for the optimal long-term operating conditions. The results showed that the CO2 absorption rate and efficiency increased under K2CO3 exposure with an increase in the pressure and loading rate. Moreover, for the temperature the absorption efficiency first increase and then decreases with increase in temperature, however, the with increase in temperature the faster absorption were observed with lower absorption loading rate. Furthermore, pH had a more complex effect due to its variable effects on the speciation of bicarbonate ions (HCO3-) and carbonate ions (CO32-). Under higher pH conditions, there was an increase in the concentration of HCO3-, which has a higher CO2 loading capacity than CO32-. Contouring maps were also used to visualize the effect of different exposure conditions on the CO2 absorption rate and efficiency and the role of 2MPz and MEA as promoters in the K2CO3 solution for CO2 absorption. The results showed that the mean CO2 absorption rate was 6.76 × 10-4 M/L/s with an R2 of 0.9693 for the K2CO3 solution containing 2MPz. The highest absorption rate (6.56-7.20 × 10-4 M/L/s) was observed at a temperature of 298-313 K, a pressure of >2 bar, a pH of 8-9, and a loading rate of 80-120 L/h for a concentration of 1-3 M K2CO3 and 0.05-1.5 M 2MPz. The CO2 absorption efficiency exhibited a variation of 56-70% under the same conditions.

Mild and Efficient One-Step Synthesis of Nitrogen-Doped Multistage Porous Carbon for High-Performance Supercapacitors.

Biomass-derived carbon materials have broad application prospects in energy storage, but still face problems such as complex synthesis paths and the massive use of corrosive activators. In this study, we proposed a mild and efficient pathway to prepare nitrogen-doped porous carbon material (N-YAC) using one-step pyrolysis with solid K2CO3, tobacco straw, and melamine. The optimized material (N-YAC0.5) was not only enriched with nitrogen, but also exhibited a high specific surface area (2367 m2/g) and a reasonable pore size distribution (46.49% mesopores). When utilized in electrodes, N-YAC0.5 exhibited an excellent capacitance performance (338 F/g at 1 A/g) in the three-electrode system, and benefitted from a high mesopore distribution that maintained a capacitance of 85.2% (288 F/g) at high current densities (20 A/g). Furthermore, the composed symmetric capacitor achieved an energy density of 14.78 Wh/kg at a power density of 400 W/kg. In summary, our work provides a novel and eco-friendly approach for converting biomass into high-performance energy-storage materials.

Catalytic Gasification of Petroleum Coke with Different Ratios of K2CO3 and Evolution of the Residual Coke Structure.

The catalytic gasification of petroleum coke with different ratios of K2CO3 was investigated by a thermogravimetric analyzer (TGA) using the non-isothermal method. The initial, peak, and final gasification temperatures of the petroleum coke decreased greatly as the amount of K2CO3 increased, and the catalytic reaction became saturated at a concentration of K+ higher than 5 mmol/g; with the further increase in catalyst; the gasification rate varied slightly, but no inhibition effect was observed. The vaporization of the catalyst was confirmed during the gasification at high temperatures. The structural evolution of the residual coke with different carbon conversions was examined by X-ray diffraction (XRD), Raman spectroscopy, and N2 adsorption analyses during gasification with and without the catalyst. The results showed that the carbon crystallite structure of the residual coke varied in the presence of the catalyst. As the carbon conversion increased, the structure of the residual coke without the catalyst became more ordered, and the number of aromatic rings decreased, while the graphitization degree of the residual coke in the presence of the catalyst decreased. Meanwhile, the surface area and pore volume of petroleum coke increased in the gasification process of the residual coke, irrespective of the presence of the catalyst. However, the reactivity of the residual coke did not change much with the variation in the carbon and pore structure during the reaction.

Use of K2CO3 to Obtain Products from Starch-Oil Mixtures by Extrusion.

Mixtures of potato starch with oils (rapeseed and sunflower) were extruded. To improve the complexation of edible oils, a catalyst was added in amounts of 3 g, 6 g, and 9 g per 100 g of sample. The aim was to obtain potato starch extrudates with a high degree of complexation and edible oils during physical modification (extrusion) with the innovative use of K2CO3 as a catalyst. Selected functional properties (water solubility index and fat absorption index) and technological properties of the obtained extrudates (radial expansion index); color in the L*, a*, and b* systems, and the specific surface area was determined from the water vapor adsorption isotherm (SBET). The fat content was determined as external, internal, or bound, and complexed by amylose to assess the degree and manner of fat complexation during extrusion. Iodine-binding capacity and the complexing index were determined to confirm the formation of amylose-lipid complexes. The incorporation of edible oils resulted in a decrease in the radial expansion index and water solubility index compared to control samples. The extrudates were dark orange. Extrudates obtained at the temperature profile L: 80/80/80/60/60/50 °C, depending on the cooking oil, complexed from 48-79% of the introduced rapeseed oil and from 36-40% of the sunflower oil. The extrusion temperature profile (H: 100/100/100/75/75/60 °C) reduced the amount of bound lipid fractions. Using potassium carbonate in the extrusion of starch-lipid systems gives hope for further increasing the share of lipids in extruded mixtures.

Chemiluminescence method based on the KIO4 -K2 CO3 -Mn2+ reaction for rapid and sensitive determination of forchlorfenuron in dried fruit.

Forchlorfenuron is a low-toxic phenylurea plant growth regulator. Excessive intake of forchlorfenuron can lead to metabolic disorders of the matrix and be harmful to human health. The chemiluminescence intensity of the KIO4 -K2 CO3 -Mn2+ reaction decreased in the presence of forchlorfenuron. Based on this result, a rapid and sensitive chemiluminescence method was established to determine forchlorfenuron by combining it with a batch injection static device. The injection speed, injection volume and reagent concentration of the forchlorfenuron-KIO4 -K2 CO3 -Mn2+ chemiluminescence reaction were optimized. Under these optimized conditions, the linear range of the method was 1.0-200.0 µg/L, and the limit of detection was 0.29 µg/L (S/N = 3). The chemiluminescence method for the determination of forchlorfenuron could be completed in 10 s. The method was applied to detect the residual forchlorfenuron in dried fruit samples, and the results are consistent with high-performance liquid chromatography-mass spectrometry. This method has the advantages of high sensitivity, rapid response, less reagent consumption, and convenient operation. It will provide a new perspective for chemiluminescence for the rapid and sensitive determination of forchlorfenuron in various complex samples.

Experimental study on carbon capture characteristics of marine engine exhaust gas by activated potassium carbonate absorbent.

Post-combustion carbon capture is a direct and effective way for onboard carbon capture. Therefore, it is important to develop onboard carbon capture absorbent that can both ensure a high absorption rate and reduce the energy consumption of the desorption process. In this paper, a K2CO3 solution was first established using Aspen Plus to simulate CO2 capture from the exhaust gases of a marine dual-fuel engine in diesel mode. The lean and rich CO2 loading results from the simulation were used to guide the selection and optimization of the activators used in the experiment. During the experiment, five amino acid salt activators including SarK, GlyK, ProK, LysK, and AlaK and four organic amine activators including MEA, PZ, AEEA, and TEPA were used. Experiments only considered the activation effect of CO2 loading between lean and rich conditions. The results showed that after adding a small amount of activator, the absorption rate of CO2 by the absorbent was greatly improved, and the activation effect of organic amine activators was stronger than that of amino acid salts. Among the amino acid salts, the SarK-K2CO3 composite solution showed the best performance in both absorption and desorption. Among the amino acid salts and the organic amino activators, SarK-K2CO3 showed the best performance in strengthening the CO2 desorption while PZ-K2CO3 enhanced the CO2 absorption process the most. In the study of the concentration ratio, it was found that when the mass concentration ratio was 1:1 for SarK:K2CO3 and PZ:K2CO3, the CO2 absorption and desorption processes improved well.

Microstructural tailoring of porous few-layer graphene-like biochar from kitchen waste hydrolysis residue in molten carbonate medium: Structural evolution and conductive additive-free supercapacitor application.

Biomass-derived graphene-like material is a promising candidate for supercapacitor electrodes, while it is critical to controllably convert biomass into structure-tunable graphene. Herein, few-layer graphene-like biochar (FLGBS) was successfully fabricated from waste biomass in molten carbonate medium. Molten carbonate acted as the effective catalyst for graphitizing and the liquid medium for microcrystal relinking to achieve the rearrangement of carbon structure. It was found that the stacking of graphene layer and formation of porous structure were influenced by the volume of reaction medium and biomass pre­carbonation. Namely, increasing the dosage of molten K2CO3 was in favor to form few layer-type graphene structure, but excess dosage could destroy the nanopore structure to expand the aperture. In addition, pre­carbonation at high temperature impeded the exfoliation of graphene layers. When FLGBSs were applied to fabricate conductive additive-free electrode, they displayed a superior supercapacitor performance (up to 237.4 F g-1 at 0.5 Ag-1). This excellent performance should be attributed to the large specific surface area, hierarchical pore structure and graphene-like structure. In short, this work could help to get insights into the structural evolution of biomass carbon to graphene-like biochar in molten carbonate medium and achieve the tailoring of microstructure for further application in energy storage.

High-Energy-Density Zinc-Air Microbatteries with Lean PVA-KOH-K2CO3 Gel Electrolytes.

Small-scale, primary electrochemical energy storage devices ("microbatteries") are critical power sources for microelectromechanical system (MEMS)-based sensors and actuators. However, the achievable volumetric and gravimetric energy densities of microbatteries are typically insufficient for intermediate-term applications of MEMS-enabled distributed internet-connected devices. Further, in the increasing subset of Internet of Things (IoT) nodes, where actuation is desired, the peak power density of the microbattery must be simultaneously considered. Metal-air approaches to achieving microbatteries are attractive, as the anode and cathode are amenable to miniaturization; however, further improvements in energy density can be obtained by minimizing the electrolyte volume. To investigate these potential improvements, this work studied very lean hydrogel electrolytes based on poly(vinyl alcohol) (PVA). Integration of high potassium hydroxide (KOH) loading into the PVA hydrogel improved electrolyte performance. The addition of potassium carbonate (K2CO3) to the KOH-PVA gel decreased the carbonation consumption rate of KOH in the gel electrolyte by 23.8% compared to PVA-KOH gel alone. To assess gel performance, a microbattery was formed from a zinc (Zn) anode layer, a gel electrolyte layer, and a carbon-platinum (C-Pt) air cathode layer. Volumetric energy densities of approximately 1400 Wh L-1 and areal peak power densities of 139 mW cm-2 were achieved with a PVA-KOH-K2CO3 electrolyte. Further structural optimization, including using multilayer gel electrolytes and thinning the air cathode, resulted in volumetric and gravimetric energy densities of 1576 Wh L-1 and 420 Wh kg-1, respectively. The batteries described in this work are manufactured in an open environment and fabricated using a straightforward layer-by-layer method, enabling the potential for high fabrication throughput in a MEMS-compatible fashion.

Efficient removal of tetracycline from aqueous solution by K2CO3 activated penicillin fermentation residue biochar.

In this study, biochar was prepared using penicillin fermentation residue (PR) as the raw material by different methods. The adsorption behavior and adsorption mechanism of biochar on tetracycline (TC) in an aqueous environment were investigated. The results showed that K2CO3 as an activator could effectively make porous structures, and that biochar with mesoporous or microporous could be prepared in a controlled manner with two kinds of different activation methods, the dry mixing method and the impregnation method. The dry mixing method could create more mesopores, while the impregnation method could prepare more micropores. Microporous biochar (IKBCH) with a high specific surface area could be prepared by the impregnation method combined with HCl soaking, which has an excellent adsorption effect on tetracycline. When the concentration of tetracycline was 200 mg/L, the removal rate of 99.91% could be achieved with the dosage of microporous biochar at 1 g/L. The adsorption process was in accordance with the Langmuir model and the pseudo-second-order model, respectively. The maximum adsorption capacity of IKBCH was 268.55 mg/g (25°C). The adsorption mechanisms were pore filling, π-π interaction, electrostatic adsorption, and hydrogen bond. Its stable and wide applicability adsorption process does not cause ecological pollution in the aqueous environment, and it is a promising biochar adsorbent.

Effect of ZnO Nanofiller on Structural and Electrochemical Performance Improvement of Solid Polymer Electrolytes Based on Polyvinyl Alcohol-Cellulose Acetate-Potassium Carbonate Composites.

In this study, a solution casting method was used to prepare solid polymer electrolytes (SPEs) based on a polymer blend comprising polyvinyl alcohol (PVA), cellulose acetate (CA), and potassium carbonate (K2CO3) as a conducting salt, and zinc oxide nanoparticles (ZnO-NPs) as a nanofiller. The prepared electrolytes were physicochemically and electrochemically characterized, and their semi-crystalline nature was established using XRD and FESEM. The addition of ZnO to the polymer-salt combination resulted in a substantial increase in ionic conductivity, which was investigated using impedance analysis. The size of the semicircles in the Cole-Cole plots shrank as the amount of nanofiller increased, showing a decrease in bulk resistance that might be ascribed to an increase in ions due to the strong action of the ZnO-NPs. The sample with 10 wt % ZnO-NPs was found to produce the highest ionic conductivity, potential window, and lowest activation energy (Ea) of 3.70 × 10-3 Scm-1, 3.24 V, and 6.08 × 10-4 eV, respectively. The temperature-frequency dependence of conductivity was found to approximately follow the Arrhenius model, which established that the electrolytes in this study are thermally activated. Hence, it can be concluded that, based on the improved conductivity observed, SPEs based on a PVA-CA-K2CO3/ZnO-NPs composite could be applicable in all-solid-state energy storage devices.

Experimental Research on the Preparation of K2CO3/Expanded Vermiculite Composite Energy Storage Material.

Thermochemical adsorption energy storage is a potential energy utilization technology. Among these technologies, the composite energy storage material prepared by K2CO3 and expanded vermiculite (EVM) shows excellent performance. In this paper, the influence of the preparation process using the impregnation method and vacuum impregnation method on K2CO3/EVM composite material is studied. The preparation plan is further optimized with the solution concentration and the expanded vermiculite particle size as variables. In the experiment, mercury intrusion porosimetry (MIP) is used to measure the porosity and other parameters. Additionally, with the help of scanning electron microscopy (SEM), the morphological characteristics of the materials are obtained from a microscopic point of view. The effects of different preparation parameters are evaluated by comparing the experimental results. The results show that the K2CO3 specific gravity of the composite material increases with the increase of the vacuum degree, up to 70.440 wt.% (the vacuum degree is 6.7 kPa). Expanded vermiculite with a large particle size (3~6 mm) can carry more K2CO3, and content per cubic centimeter of K2CO3 can be as high as 0.466 g.

The investigation of activated carbon by K2CO3 activation: Micropores- and macropores-dominated structure.

In this study, the K2CO3 activation of bamboo was investigated in detail, and the structure and properties of the prepared activated carbons were tested for the feasibility of CO2 capture application and the potential for both ion and bacteria adsorption for use in the field of hazardous wastewater treatment. Activated carbons were produced with different activator ratios, from 0.5 to 6 according to the sample mass ratio. The ratio of H or O to C (H/C or O/C) increased with the increasing amount of K2CO3 added for the activation. The samples had a highly-porous microporous structure, in which the micropore volume was calculated to be 0.6 cm3 g-1 by the DR method of the CO2 adsorption isotherm at 298 K. The BET surface area and total pore volume estimated from the N2 adsorption isotherms at 77 K of the activated materials increased according to the increase of the K2CO3 impregnation ratio to a maximum value of 1802 m2 g-1 and 0.91 cm3 g-1, respectively. Moreover, the K2CO3-activated samples had a specific morphology, that is, macropores which are presumed to be derived from bubbles. The X-ray-CT images showed that the bubble-like structure is not only on the surface but also inside the samples. The results of gas adsorption methods, mercury porosimetry, and SEM showed the co-existence of micropores (<2 nm) and macropores (100-10,000 nm). The results highlighted the unique pore structure, that is, the coexistence of micropores and macropores that would contribute to forming solutions for carbon sequestration in the atmosphere and wastewater treatment.

Assay system for mesocotyl elongation and hydrotropism of maize primary root in response to low moisture gradient.

We designed and validated a test system that simulates a growth environment for Zea mays L. maize seedlings under conditions of low moisture gradient in darkness. This system allowed us to simultaneously measure mesocotyl elongation and the primary root hydrotropic response in seedlings before the emergence phase in a collection of maize hybrids. We found great variation in these two traits with statistically significant reduction of their elongations under the low moisture gradient condition that indicate the richness of maize genetic diversity. Hence, the objective of designing a new test system that evaluates the association between these underground traits with the potential use to measure other traits in maize seedlings related to early vigor was achieved.

Co-pyrolysis of sewage sludge/cotton stalks with K2CO3 for biochar production: Improved biochar porosity and reduced heavy metal leaching.

The co-pyrolysis of sewage sludge and biomass is considered a promising technique for reducing the volume of sewage sludge, adding value, and decreasing the risk associated with this waste. In this study, sewage sludge and cotton stalks were pyrolyzed together with different amounts of K2CO3 to evaluate the potential of chemical activation using K2CO3 for improving the porosity of the biochar formed and immobilizing the heavy metals present in it. It was found that K2CO3 activation effectively improved the pore structure and increased the aromaticity of the biochar. Moreover, K2CO3 activation transformed the heavy metals (Cu, Zn, Pb, Ni, Cr, and Cd) into more stable forms (oxidizable and residual fractions). The activation effect became more pronounced with increasing amount of added K2CO3, eventually resulting in a significant reduction in the mobility and bioavailability of the heavy metals in the biochar. Further analysis revealed that, during the co-pyrolysis process, K2CO3 activation resulted in a reductive atmosphere, increased the alkalinity of the biochar, and led to the formation CaO, CaCO3, and aluminosilicates, which aided the immobilization of the heavy metals. K2CO3 activation also effectively reduced the leachability, and thus, the environmental risks of the heavy metals. Thus, K2CO3 activation can improve the porosity of the biochar derived from sewage sludge/cotton stalks and aid the immobilization of the heavy metals in it.

Optimization of the Electrochemical Performance of a Composite Polymer Electrolyte Based on PVA-K2CO3-SiO2 Composite.

Composite polymer electrolyte (CPE) based on polyvinyl alcohol (PVA) polymer, potassium carbonate (K2CO3) salt, and silica (SiO2) filler was investigated and optimized in this study for improved ionic conductivity and potential window for use in electrochemical devices. Various quantities of SiO2 in wt.% were incorporated into PVA-K2CO3 complex to prepare the CPEs. To study the effect of SiO2 on PVA-K2CO3 composites, the developed electrolytes were characterized for their chemical structure (FTIR), morphology (FESEM), thermal stabilities (TGA), glass transition temperature (differential scanning calorimetry (DSC)), ionic conductivity using electrochemical impedance spectroscopy (EIS), and potential window using linear sweep voltammetry (LSV). Physicochemical characterization results based on thermal and structural analysis indicated that the addition of SiO2 enhanced the amorphous region of the PVA-K2CO3 composites which enhanced the dissociation of the K2CO3 salt into K+ and CO32- and thus resulting in an increase of the ionic conduction of the electrolyte. An optimum ionic conductivity of 3.25 × 10-4 and 7.86 × 10-3 mScm-1 at ambient temperature and at 373.15 K, respectively, at a potential window of 3.35 V was observed at a composition of 15 wt.% SiO2. From FESEM micrographs, the white granules and aggregate seen on the surface of the samples confirm that SiO2 particles have been successfully dispersed into the PVA-K2CO3 matrix. The observed ionic conductivity increased linearly with increase in temperature confirming the electrolyte as temperature-dependent. Based on the observed performance, it can be concluded that the CPEs based on PVA-K2CO3-SiO2 composites could serve as promising candidate for portable and flexible next generation energy storage devices.

An overview on medicinal perspective of thiazolidine-2,4-dione: A remarkable scaffold in the treatment of type 2 diabetes.

Diabetes or diabetes mellitus is a complex or polygenic disorder, which is characterized by increased levels of glucose (hyperglycemia) and deficiency in insulin secretion or resistance to insulin over an elongated period in the liver and peripheral tissues. Thiazolidine-2,4-dione (TZD) is a privileged scaffold and an outstanding heterocyclic moiety in the field of drug discovery, which provides various opportunities in exploring this moiety as an antidiabetic agent. In the past few years, various novel synthetic approaches had been undertaken to synthesize different derivatives to explore them as more potent antidiabetic agents with devoid of side effects (i.e., edema, weight gain, and bladder cancer) of clinically used TZD (pioglitazone and rosiglitazone). In this review, an effort has been made to summarize the up to date research work of various synthetic strategies for TZD derivatives as well as their biological significance and clinical studies of TZDs in combination with other category as antidiabetic agents. This review also highlights the structure-activity relationships and the molecular docking studies to convey the interaction of various synthesized novel derivatives with its receptor site.

Synergistic conversion of coal char and methane for syngas and carbon-based supercapacitor electrodes.

A facile one-pot process for synergistic conversion of coal char and methane is conducted by employing K2CO3 as the catalyst. Besides syngas production, valuable carbon products are obtained and used to serve for supercapacitor electrodes. Effect of the operating parameters (including the catalyst dosage, gas feed flow rate, reaction temperature and time) is evaluated on electrochemical performance of the as-prepared carbon. The appropriate surface and structural properties enable the prepared carbon electrode to have a remarkable capacitive performance, along with a specific capacitance up to 125 F/g at a scan rate of 5 mV/s and 133 F/g at a current density of 1 A/g. According to the potential capacitive contribution of the carbon species, the high capacitive performance is mainly attributed to formation and growth of abundant carbon fibers in the one-pot process.