Inorganic Constituents Research Articles

Passivation Layers in Mg-Metal Batteries: Robust Interphases for Li-Metal Batteries.

In advanced batteries, interphases serve as the key component in stabilizing the electrolyte with reactive electrode materials far beyond thermodynamic equilibria. While an active interphase facilitates the transport of working ions, an inactive interphase obstructs ion flow, constituting the primary barrier to the realization of battery chemistries. Here, a successful transformation of a traditionally inactive passivating layer on Mg-metal anode, characteristic of Mg-metal batteries with typical carbonate electrolytes, into an active and robust interphase in the Li-metal scenario is presented. By further strategically designing magnesiated Li+ electrolytes, the in situ development of this resilient interphase on Li-metal anodes, imparting enduring stability to Li-metal batteries with nickel-rich cathodes is induced. It is identified that the strong affinity between Mg2+ and anions in magnesiated Li+ electrolytes assembles ionic clusters with a bias for reducibility, thereby catalyzing the creation of anion-derived interphases rich in inorganic constituents. The prevalence of ionic clusters induced by magnesiation of electrolytes has brought properties only available in high-concentration electrolytes, suggesting a fresh paradigm of tailing electrolytes for highly reversible LMBs.

Depth-resolved elemental and molecular analysis of polymeric multilayers with EI-MS and ICP-OES using chemometric evaluation

Polymeric composite materials with layered structures have increasingly gained importance as, for specific applications, the required properties cannot be achieved with one single material; thus, for example, multi-layer polymers or special surface coatings are employed.None of the conventionally available techniques enables a comprehensive characterization of composite materials, including depth-resolved information about their organic and elemental constituents.In this work, a previously introduced approach enabling the direct characterization of the organic and inorganic constituents of solid polymer samples was further developed and optimized for depth profiling analysis of stacked layer polymers. For this purpose, the ablation chamber’s washout behavior and transfer line’s transport efficiency were improved. Chemometric methods were applied for the data analysis to gain greater insight and enable more precise differentiation, comparison and classification.The work investigates the feasibility of the developed approach by analyzing a multi-layer stacked polymer sample created from nail polishes and using cluster analysis on the data collected with the bimodal detection. The layers of the sample could be differentiated by their organic and elemental constituents’ fingerprints, achieving a depth resolution of 7 µm.

Luminescent Alendronic Acid-Conjugated Micellar Nanostructures for Potential Application in the Bone-Targeted Delivery of Cholecalciferol

Vitamin D, an essential micronutrient crucial for skeletal integrity and various non-skeletal physiological functions, exhibits limited bioavailability and stability in vivo. This study is focused on the development of polyethylene glycol (PEG)-grafted phospholipid micellar nanostructures co-encapsulating vitamin D3 and conjugated with alendronic acid, aimed at active bone targeting. Furthermore, these nanostructures are rendered optically traceable in the UV–visible region of the electromagnetic spectrum via the simultaneous encapsulation of vitamin D3 with carbon dots, a newly emerging class of fluorescents, biocompatible nanoparticles characterized by their resistance to photobleaching and environmental friendliness, which hold promise for future in vitro bioimaging studies. A systematic investigation is conducted to optimize experimental parameters for the preparation of micellar nanostructures with an average hydrodynamic diameter below 200 nm, ensuring colloidal stability in physiological media while preserving the optical luminescent properties of the encapsulated carbon dots. Comprehensive chemical-physical characterization of these micellar nanostructures is performed employing optical and morphological techniques. Furthermore, their binding affinity for the principal inorganic constituent of bone tissue is assessed through a binding assay with hydroxyapatite nanoparticles, indicating significant potential for active bone-targeting. These formulated nanostructures hold promise for novel therapeutic interventions to address skeletal-related complications in cancer affected patients in the future.

Rod-shaped Mo(vi) trichalcogenide–Mo(vi) oxide decorated on poly(1-H pyrrole) as a promising nanocomposite photoelectrode for green hydrogen generation from sewage water with high efficiency

Abstract The synthesis of rod-shaped Mo(vi) trichalcogenide–Mo(vi) oxide, cleverly adorned on a poly(1-H pyrrole) (P1HP) matrix (MoS3–MoO3/P1HP), is achieved through a one-pot preparation method. This process occurs under the pyrrole oxidation employing the oxidizing agent Na2MoO4. Notably, this oxidation process facilitates the direct incorporation of the inorganic constituents into the polymer matrix. Of particular significance is the material’s bandgap, which is optimally situated at 1.4 eV, rendering it highly suitable for its intended applications. The material assumes a rod-like structure, characterized by an average length of 400 nm and width of 30 nm, further enhancing its desirability. In practice, this thin film serves as an exceptionally promising photoelectrode. It finds its forte in the generation of hydrogen from sewage water, achieving an impressive efficiency rate of 12.66%, specifically at 340 nm. In addition to that, it boasts a remarkable hydrogen generation rate of 1.2 moles·h−1·cm−2. Moreover, the material exhibits remarkable versatility in its response to light. Its sensitivity to monochromatic light across a broad optical spectrum (UV till IR), underscores its potential for hydrogen generation applications for industrial applications.

Insights into the generation of multiple reactive species in UV254/PMS/I− system and their roles for degradation of phenolic and non-phenolic pollutants

An innovative technology for the removal of phenolic and non-phenolic organic pollutants from aqueous solution was developed by combining UV254 irradiation, peroxymonosulfate (PMS), and iodide ions (I−). Effects of pH, ratio of [I−]/[PMS], initial concentration of pollutant, dissolved organic matter (DOM) and typical inorganic constituents of environmental water on the degradation of studied pollutants with UV254/PMS/I− system were examined. The results showed that pH and [I−]/[PMS] exhibited significant impact on the degradation of pollutants during UV254/PMS/I− process. As the ratio of [I−]/[PMS] increased from 0.1 to 10.0, the removal efficiencies of phenolic pollutants remarkably increased, but those of non-phenolic pollutants decreased. The DOM at high concentration obviously inhibited the degradation of pollutants during UV254/PMS/I− process. Meanwhile, the occurrence of NO3− can slightly enhance the degradation of pollutants, and SO42−, Cl−, and HCO4− ions had no significant effects on UV254/PMS/I− system. The abundant reactive species including OH, SO4−, and I/I2− during UV254/PMS/I− process were generated based on electron spin resonance, fluorescence spectroscopy and steady-state concentration analysis. Quenching experimental results indicated that I/I2− can selectively degrade phenolic pollutants via one-electron oxidation. This study provided a reference for the application of reactive radicals involved oxidative technique in water purification.

Ingenious Architecture and Coloration Generation in Enamel of Rodent Teeth.

Teeth exemplify architectures comprising an interplay of inorganic and organic constituents, resulting in sophisticated natural composites. Rodents (Rodentia) showcase extraordinary adaptations, with their continuously growing incisors surpassing human teeth in functional and structural optimizations. In this study, employing state-of-the-art direct atomic-scale imaging and nanoscale spectroscopies, we present compelling evidence that the release of material from ameloblasts and the subsequent formation of iron-rich enamel and surface layers in the constantly growing incisors of rodents are complex orchestrated processes, intricately regulated and independent of environmental factors. The synergistic fusion of three-dimensional tomography and imaging techniques of etched rodent́s enamel unveils a direct correlation between the presence of pockets infused with ferrihydrite-like material and the acid resistant properties exhibited by the iron-rich enamel, fortifying it as an efficient protective shield. Moreover, observations using optical microscopy shed light on the role of iron-rich enamel as a microstructural element that acts as a path for color transmission, although the native color remains indistinguishable from that of regular enamel, challenging the prevailing paradigms. The redefinition of "pigmented enamel" to encompass ferrihydrite-like infusion in rodent incisors reshapes our perception of incisor microstructure and color generation. The functional significance of acid-resistant iron-rich enamel and the understanding of the underlying coloration mechanism in rodent incisors have far-reaching implications for human health, development of potentially groundbreaking dental materials, and restorative dentistry. These findings enable the creation of an entirely different class of dental biomaterials with enhanced properties, inspired by the ingenious designs found in nature.

Efficiently tuning the electrical performance of PBTTT-C14 thin film via in situ controllable multiple precursors (Al2O3:ZnO) vapor phase infiltration

Conjugated polymer-based organic/inorganic hybrid materials become the current research frontier and show great potential to integrate flexible polymers and rigid solid materials, which have been widely used in the field of various flexible electronics and optical devices. In this study, based on the multiple vapor phase infiltration (VPI) process, various precursor molecules (diethylzinc DEZ, trimethylaluminum TMA, H2O) are applied for the in situ modification of PBTTT-C14 films. The conductivity of the PBTTT-C14/Al2O3:ZnO (AZO) film is significantly enhanced, and the maximum value of conductivity is 1.16 S cm−1, which is eight orders of magnitude higher than the undoped PBTTT-C14 thin film. Here, the change of morphologies and crystalline states are analyzed via SEM, AFM, and XRD. And the chemical changes during the VPI process of PBTTT-C14 are characterized through Raman, XPS, and UV–vis. During the AZO VPI process, the formation of new ZnS matrix in the polymer subsurface can generate new additional electron conduction pathways through the crosslinking of polymer chains with inorganic materials, and the addition of Al2O3 can bring about the increase of average grain size of ZnO crystals, which is also benefit to the conductivity increase of PBTTT-C14 thin film. Generally, the synergistic effect between the inorganic and polymer constituents results in the significantly enhancement of the conductivity of PBTTT-C14/AZO thin films.

Inorganic and organic chemical constituents of trona, alum and palm ash: Potential alternatives to conventional antifungal drugs?

There is high demand for the development of novel, effective, clinically safe and affordable antifungal agents to manage the ever emerging and re-emerging fungal infections. Natural compounds may be a source of novel chemical structures for development of antimicrobials. The aim of this study was to determine the inorganic and organic chemical constituents of trona, alum and palm ash; as potential alternatives to conventional antifungal drugs. The fungal isolates were obtained from high vaginal swab samples of patients suffering from vulvo-vaginal candidiasis. The isolates were identified based on their macroscopic, physiological, biochemical and molecular characteristics. The minimal inhibitory concentration (MIC) and minimal fungicidal concentrations (MFC) of the test agents were determined using the broth dilution method. Gas chromatography-mass spectroscopy (GC-MS) was used to determine the organic constituents; while x-ray fluorescence spectroscopy, for inorganic constituents. The isolates include Candida albicans, C. tropicalis, C. glabrata and C. parapsilosis. The MIC and MFC of alum against the isolates ranged from 12.50 mg/ml to 50 mg/ml, trona (6.25 mg/ml to 100 mg/ml) and palm ash (100 mg/ml to 200 mg/ml). Alum comprises oxides of sulphur (44.5 %), aluminium (14.49 %) while lead, arsenic and nickel all accounted for <0.0010 %. The naturally occurring fatty acids include vaccenic acid (40.39 %), decanoic acid (13.21 %) and linoelaidic acid (9.84 %). Trona comprises of sulphur (2.14 %), chlorine (5.8 %), potassium (1.7 %), lead (0 %), arsenic and nickel (<0.003 %); while the organic constituents include linoelaidic acid (32.99 %), nonanoic acid (14.81 %) and decanoic acid (6.8 %). The inorganic components of palm ash include potassium (28.8 %), sulphur (3.4 %), calcium (2.8 %) and chlorine (15 %) while the heavy metals all accounted for <0.0007 %. The organic constituents were urea (8.65 %) and fatty acids (<6 %). The antimicrobial properties of the natural compounds were probably due to their various organic and inorganic constituents; thus, could serve as potential raw materials in antifungal drugs production.

Inorganic geochemical attributes of Jaintia Hills coals, India: Implications for paleo-depositional conditions

The Paleogene coal deposits of the Jaintia Hills of Meghalaya have undergone examinations by various researchers, primarily focusing on organic petrography and geochemistry and highlighting the rank, type, and grade, with perspectives on potential utilization. However, the genesis of these coals has received limited attention from the researchers. This research article addresses this gap by conducting a comprehensive examination of the geochemical and mineralogical aspects of these coals. Coal samples from two coal seams at nine locations in the Sampar coalfield in Jaintia Hills were collected and studied. The samples are subjected to X-ray fluorescence spectroscopy, X-ray diffraction analyses, Fourier transform infrared spectroscopy, proximate, and ultimate analysis to study geochemical and mineralogical composition and ash yield. The study utilizes various geochemical proxies based on the inorganic constituents, providing insights into the paleo-depositional conditions and contributing to a deeper understanding of the unique characteristics of Meghalayan coals. The research indicates that these coals were formed in coastal swamps and lagoons on stable platforms, experiencing minimal tectonic activity, influenced by seawater incursions. These coals were deposited in reducing to significantly reducing conditions and warm and humid to semi-arid climatic conditions. No signature of a geothermally active fluid has been recorded.

Biosolids management and utilizations: A review

Biosolids, derived from wastewater treatment processes, have garnered increasing attention as a valuable resource due to their rich organic and inorganic constituents, which can be beneficially utilized in multiple sectors, including agriculture, civil engineering, and energy recovery. The present review article begins by providing an overview of biosolids, including their production methods and classification based on treatment processes. Subsequently, the chemical composition of biosolids is explored, highlighting the diverse array of organic and inorganic components present. The characterization techniques employed for analyzing biosolids, such as spectroscopy, chromatography, and microscopy, are thoroughly discussed, emphasizing their role in determining the quality and suitability of biosolids for different applications. Furthermore, the environmental impacts associated with biosolids disposal are extensively examined. This includes the potential risks posed by heavy metals, pathogens, and emerging contaminants, as well as strategies for mitigating these risks through proper treatment and management practices. In addition to environmental considerations, the article explores the various products that can be derived from biosolids. These include organic matter-rich soil amendments for agricultural applications, inorganic nutrient supplements for enhancing plant growth, and the potential for energy recovery through anaerobic digestion and thermal conversion technologies. The utilization of biosolids in civil engineering projects, such as landfill capping and construction materials, is promising. Land application of biosolids also can have economic and waste management benefits (e.g., conservation of landfill space; reduced demand on non-renewable resources like phosphorus; and a reduced demand for synthetic fertilizers).

Fabrication and Characterization of Granulated β-Tricalcium Phosphate and Bioactive Glass Powders by Spray Drying

Biocomposite materials are widely implemented in various applications in clinical dentistry and orthopedics since it is possible to combine multiple materials by relying on their compatibility. Ceramic-based materials have osteogenic and osteoconductive features owing to their inorganic constituents with dental and bone tissue. β-tricalcium phosphate (β-TCP) and bioactive glass have excellent biocompatibility, bioresorbability, and bioactivity. In this study, β-TCP and BG powders were fabricated by spray pyrolysis (SP) and spray drying (SD). These fabrication methods are suitable for the mass production and synthesis of spherical particles. At first, β-TCP and BG spherical particles were synthesized by SP and characterized using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and scanning electronic microscopy (SEM). After that, these powders were granulated with the different weight ratios of β-TCP/BG = 100/0, 75/25, 50/50, 25/75, and 0/100 by SD. The resulting granulation powders were characterized using XRD, FT-IR, and SEM to investigate phase compositions and microstructures. In addition, cytotoxicity was investigated using the MTT assay.

Soil adsorption potential: Harnessing Earth's living skin for mitigating climate change and greenhouse gas dynamics

Soil adsorption, which could be seen as a crucial ecosystem service, plays a pivotal role in regulating environmental quality and climate dynamics. However, despite its significance, it is often undervalued within the realms of research and policy frameworks. This article delves into the multifaceted aspects of soil adsorption, incorporating insights from chemistry and material science, ecological perspectives, and recent advancements in the field. In exploring soil components and their adsorption capacities, the review highlights how organic and inorganic constituents orchestrate soil's aptitude for pollutant mitigation and nutrient retention/release. Innovative materials and technologies such as biochar are evaluated for their efficacy in enhancing these natural processes, drawing a link with the sustainability of agricultural systems. The symbiosis between soil microbial diversity and adsorption mechanisms is examined, emphasizing the potential for leveraging this interaction to bolster soil health and resilience. The impact of soil adsorption on global nutrient cycles and water quality underscores the environmental implications, portraying it as a sentinel in the face of escalating anthropogenic activities. The complex interplay between soil adsorption mechanisms and climate change is elaborated, identifying research gaps and advocating for future investigations to elucidate the dynamics underpinning this relation. Policy and socioeconomic aspects form a crucial counterpart to the scientific discourse, with the review assessing how effective governance, incentivization, and community engagement are essential for translating soil adsorption's functionality into tangible climate change mitigation and sustainable land-use strategies. Integrating these diverse but interconnected strata, the article presents a comprehensive overview that not only charts the current state of soil adsorption research but also casts a vision for its future trajectory. It calls for an integrated approach combining scientific inquiry, technological innovation, and proactive policy to leverage soil adsorption's full potential to address environmental challenges and catalyze a transition towards a more sustainable and resilient future.

Investigations of Morphology and Carrier Transport Characteristics in High‐Performance PEDOT:PSS/Tellurium Binary Composite Fibers Produced via Continuous Wet‐Spinning

AbstractFiber‐based flexible thermoelectric (TE) generators are highly desirable due to their capability to convert thermal energy into electricity and their potential applications in wearable electronics. High‐performance poly(3,4‐ethylene dioxythiophene):poly(styrene sulfonate) (PEDOT:PSS)/Tellurium (Te) composite TE fibers have been successfully developed via a continuous wet‐spinning approach followed by sulphuric acid treatment. With a simple pre‐modification to Te nanowires, the inorganic Te fillers form uniform distribution in PEDOT:PSS. At the optimal condition, the composite fibers exhibit a power factor of 233.5 µW m−1 K−2 and mechanical strength of 205 MPa, which are among the highest values reported so far for the PEDOT:PSS‐based TE fibers. From the viewpoint of TE property enhancement mechanism, understanding the morphology and carrier transport behavior in the 1D organic/inorganic composite fibers remains still challenging. On basis of a series of PEDOT:PSS/Te composite fibers with varying Te fractions, orientations of both the inorganic and organic constituents are quantitatively evaluated. Their electrical conductivities and Seebeck coefficients are also analyzed with modified series‐parallel models and energy filtering theory. This work may not only provide a universal approach to produce high‐performance organic/inorganic composite TE fibers for various wearable applications, but also help to understand the morphology and charge transport between heterogeneous phases in a 1D composite.

Fecal biomarkers in Italian anthropogenic soil horizons and deposits from Middle Ages and bronze age

Archaeological excavations in urban and rural contexts often uncover dark homogeneous anthropogenic deposits, soils and soil horizons, known as Dark Earths, Cultural Layers and Anthrosols. Major scientific questions arise about the processes that lead to the formation of these soils and deposits, as they are often related to a complex combination of environmental, climatic, and anthropogenic factors. Many studies focused on the morphological and physical-chemical investigation of the archaeological remains found as well as the inorganic constituent of the soil. The organic fraction has been only roughly investigated and studies carried out on a molecular level are very limited. However, a more refined investigation of the chemical constituents of these soils can potentially reveal pivotal insights on the archaeological context such as past domestic habits and/or urban organization. It has been demonstrated that, among organic matter constituents, fecal steroids are promising biomarkers to track fecal input in many environmental matrixes such as water, soils, and sediments. In this paper we determine the fecal sterols and stanols content in dark homogeneous anthropogenic deposits and soils found in seven archaeological sites in Italy (from Verona, Como, Florence, Mel and Conegliano) dated from the Late Bronze Age and the Medieval Period, aiming to assess the major contribution of the fecal input using diagnostic fecal indexes obtained from specific fecal sterol proportions. To this purpose, a baseline was established by identifying the fecal fingerprint of domestic herbivores (caprids, ovines, equines and bovines) and omnivores (pigs). Based on their fecal fingerprint, we classified the deposits of seven studied sites into four distinct categories: i) the medieval sites of Verona, presented a strong mixed fecal input from both herbivores and humans; ii) the medieval sites of Como and Florence which showed a similar pattern, with a predominance of human fecal input over livestock; iii) the late medieval soils of Mel and the late bronze age Cultural Layers of Castellar di Leppia (Verona) which exhibited a generally scarce fecal contamination while iv) the final bronze age site of Conegliano (Treviso), a strong fecal contamination from herbivores was detected. These results thus demonstrate that for the Medieval Dark Earth the socio-cultural processes leading to the formation of the Dark Earth differ in terms of sewage and waste management and/or in animal husbandry practices.

Chemical composition and potential antioxidant, anti-inflammatory, and analgesic efficacy of Cistus albidus L.

This study aims to assess the chemical composition of the aqueous extract of Cistus albidus L. leaves, as well as the potential of aqueous and hydroethanol extracts of the leaves and seeds as analgesic, anti--inflammatory, and antioxidant agents. The contents of phenolics and inorganic constituents were determined in C. albidus seeds and leaves; antioxidant capacity was assessed by 3 complementary and diverse tests. The carrageenan-induced paw edema technique was used to investigate the anti-inflammatory effect in vivo, and albumin denaturation to evaluate the anti-inflammatory effect in vitro. The acetic acid-induced contortion test, the tail-flick test, and the plantar test were used to assess the analgesic effi cacy in vivo. Chemical analysis was performed by UPLC-MS/MS to quantify several phenolic compounds including catechin (1,627.6 mg kg-1), quercitrin (1,235.8 mg kg-1) and gallic acid (628. 2 mg kg-1). The ICP analysis revealed that potassium and calcium were the main inorganic components in the seeds and leaves of C. albidus. The hydroethanolic extract of the leaves showed the highest content of polyphenols/flavonoids, whereas the highest value of proantho cyanidins was detected in the aqueous extract of the seeds. All extracts showed potent antioxidant activity related to different phenolic compounds (quercetin, gallic acid, astragalin, catechin, and rutin). The aqueous extract of the leaves strongly inhibited paw edema (76.1 %) after 6 h of treatment and showed maximal inhibition of protein denaturation (191.0 µg mL-1 for 50 % inhibition) and analgesic activity in different nociceptive models. The presented data reveal that C. albidus extracts potentially show antioxidant, anti-inflammatory, and analgesic activities that could confirm the traditional use of this plant.

Atmospheric aerosol chemistry and source apportionment of PM10 using stable carbon isotopes and PMF modelling during fireworks over Hyderabad, southern India

This study examined the influence of fireworks on atmospheric aerosols over the Southern Indian city of Hyderabad during festival of Diwali using mass closure, stable carbon isotopes and the EPA-PMF model. Identification of chemical species in day and night time aerosol samples for 2019 and 2020 Diwali weeks showed increased concentrations of NH4+, NO3−, SO42−, K+, organic carbon (OC), Ba, Pb and Li, which were considered as tracers for fireworks. PM10 source apportionment was done using inorganic (trace elements, major ions) and carbonaceous (organic and elemental carbon; OC & EC) constituents, along with stable isotopic compositions of TC and EC. K+/Na+ ∼1 and K+nss/OC > 0.5 indicated contribution from fireworks. High NO3−, NH4+, Na+, Cl− and SO42− suggested the presence of deliquescent salts NaCl, NH4NO3 and (NH4)2SO4. TAE/TCE >1 suggested H+ exclusion, indicating possible presence of H2SO4 and NH4HSO4 in the aerosols. Ba, Pb, Sb, Sr and Fe increased by 305 (87), 12 (11), 12 (3), 3 (2) and 3 (4) times on Diwali nights, compared to pre-Diwali of 2019 (2020), and are considered as metallic tracers of fireworks. δ13CTC and δ13CEC in aerosols closely resembled that of diesel and C3 plant burning emissions, with meagre contribution from firecrackers during Diwali period. The δ13CEC was relatively depleted than δ13CTC and δ13COC. For both years, δ13COC-EC (δ13COC - δ13CEC) were positive, suggesting photochemical aging of aerosols during long-range transport, while for pre-Diwali 2019 and post-Diwali 2020, δ13COC-EC were negative with high OC/EC ratio, implying secondary organic aerosols formation. High toluene during Diwali week contributed to fresh SOA formation, which reacted with precursor 12C, leading to 13C depletions. Eight-factored EPA-PMF source apportionment indicated highest contribution from residue/waste burning, followed by marine/dust soil and fireworks, while least was contributed from solid fuel/coal combustion.

Construction of robust solid-electrolyte interphase via electrode additive for high-performance Sn-based anodes of sodium-ion batteries

Alloy-based Sn anode for sodium-ion batteries has attracted tremendous attention due to its low working voltage, high specific capacity, and good availability. Its application is hindered, however, by inferior cycling stability due to its huge volume changes and unstable solid-electrolyte interphase (SEI) film. Herein, tetraphenylphosphonium bis(trifluoromethanesulfonyl)imide (TPPTFSI) is introduced into the electrode and spontaneously adsorbed on the surfaces of commercial Sn microparticles (μ-Sn) to improve the electrochemical performance of the Sn anode. In the first cycle, the TPP+ component of TPPTFSI decomposes to form an organic component of the SEI film, thereby enhancing its flexibility. Meanwhile, the TFSI− component is converted into an inorganic constituent of the SEI, improving its robustness and ionic conductivity. Therefore, the cycling performance of the μ-Sn is enhanced significantly. The modified electrode, TPPTFSI-Sn, delivers a capacity of 619.7 mAh g−1 after 2000 cycles at 2.0 A g−1, while the control sample can only survive for 30 cycles. Importantly, the full cell also exhibits excellent performance, including rate performance and cycling stability. Its simple operation and remarkable electrochemical performance improvement indicate the promising prospects of this strategy for advanced electrodes in SIBs.

A New Methodological Approach to Study the Interaction of Humic Acids, Minerals and Polyvalent Cations in Soil

ABSTRACT A new methodological approach of humic acid (HA) extraction is applied to study soil samples with contrasting management regimes: natural vegetation (NV) and agricultural (A). This innovative approach involves a modification of the Swift’s method, wherein several steps HCl/HF are replaced by a single-step HCl/HF. This modification enabled us to investigate the ability of HA to retain inorganic constituents. The carbon content was significantly higher in soils under NV (19.8–27.3 g C kg−1) than under A (11.2–13.4 g C kg−1). The same pattern was observed for the HA content. The new methodology revealed that HA from NV soils had a much higher capacity to retain inorganics (ash contents in HA from 12.3–28.3%) than in A soils (ash content in HA from 1.6–2.6%). Similar results were found for Ca+Al+Fe contents in the HA (3.7–2.5 meq g−1 in HA from NV soils; 2.2–.9 meq g−1 in HA from A soils). Some differences were observed in IR spectra, mainly an intense band at around 1050 cm−1 of HA from NV that reflects the high ash content of the HA and its capacity of retaining inorganic material. Ca binding isotherms of HA also showed that the HA differed significantly in their ability to retain inorganic components when extracted. Humic acid from NV was more efficient in retaining metal ions and minerals than HA from A soils. All results point to a better contact between organic and inorganic matter in NV soils, and this contact contributes to the stabilization of organic matter.

Direct Liquefaction of South African Vitrinite- and Inertinite-Rich Coal Fines.

In this investigation, coal fines enriched with inertinite were used for direct liquefaction experiments. For comparison, a vitrinite-rich coal typically utilized in coal-to-liquid processes was also employed. To assess the impact of mineral matter content, demineralization was used to remove most of the inorganic constituents. The findings revealed that the inertinite-rich coal exhibited lower liquefaction conversions due to a reduced proportion of reactive macerals and elevated levels of inorganic mineral matter. These conversion values exhibited a strong correlation with the quantity of reactive macerals present in the parent coals. For the inertinite-rich coal, the presence of inorganic mineral matter impeded the liquefaction process but facilitated the CO2 gasification reactions of the derived chars. To evaluate their potential in gasification processes, CO2 gasification experiments were conducted and the reactivities and apparent gasification activation energies of both coal chars, liquefaction residue chars, and preasphaltene and asphaltene (PAA) chars were calculated. These calculations were carried out using the random pore model (RPM) and volumetric reaction model (VRM). The chemistry, reactivity, and kinetics of residue gasification conversion are not thoroughly understood, yet they hold significant importance in optimizing syngas production within gasification processes. The findings from this work highlight significant differences in liquefaction conversion values, product distribution, and composition. These differences are influenced by factors such as maceral composition, inorganic mineral matter content, hydrogen-donor capabilities of the solvent, and liquefaction reaction temperatures. Additionally, these variables affect the CO2 gasification reactivity of liquefaction solid residue chars.

Persulfate Activation Using Biochar from Pomegranate Peel for the Degradation of Antihypertensive Losartan in Water: The Effects of Pyrolysis Temperature, Operational Parameters, and a Continuous Flow Reactor

Biochar derived from pomegranate peel at different pyrolysis temperatures (450, 600, and 850 °C) was synthesized and characterized by BET, XRD, FTIR, and SEM-EDX. Its catalytic efficiency in the degradation of the antihypertensive losartan (LOS) in the presence of sodium persulfate was examined. The biochar pyrolyzed at 850 °C exhibited higher catalytic activity, which was correlated with the greater surface area and higher concentration of minerals on its surface. Interestingly, despite adsorption being favored at alkaline pH, pH 3 showed the highest LOS degradation. LOS decomposition followed pseudo-first-order kinetics. The addition of persulfate significantly increased LOS reduction, while the presence of inorganic and organic water matrix constituents such as sodium chloride, bicarbonate, and humic acid inhibited the oxidation. Experiments conducted with radical scavengers revealed that both hydroxyl and sulfate radicals, as well as singlet oxygen, participated in LOS decomposition, with the former being the dominant species. Using a continuous flow reactor, the system exhibited a satisfactory steady-state performance of 90% LOS removal for 114 h. Afterward, a moderate decrease in performance was observed, which can be attributed to the alteration of the catalyst’s surface and mineral dissolution due to acidity.