Morphological Structure Research Articles

Dope dyeing of tannic acid modified ultra‐high molecular weight polyethylene fabric

AbstractIn this study, we examined dyeing behavior of tannic acid modified ultra high molecular weight polyethylene fabric. Whole study was conducted to see the effect of tannic acid on dope dyeing performance of the fabric. Tannic acid and its complex with sodium salt TA‐Na+ complex were used for pretreatment. After dope dyeing, the color strength of fabrics, color fastness, surface morphology, and fiber structure were characterized by k/s value, color difference, scanning electron microscopy (SEM), electron dispersive spectroscopy (EDS), and Fourier transform infrared spectroscopy (FTIR), respectively. The effect of treatment conditions was also discussed. The results had shown better color strength and washing fastness were obtained after tannic acid treatment, especially after TA‐Na+ complex treatment. SEM observation indicated the tannic acid adhesion on fabric surface. Both EDS and FTIR results showed the enhancement of surface polarity. And the UHMWPE fabric treated with 1% (w/v) TA‐Na+ with pH ranging 4–5 for 6 h showed better color durability over time. Approach was suitable because of sustainable, green behavior of tannic acid and entire process had a low cost.

Electronic Structure and Functions of Carbon Nitride in Frontier Green Catalysis.

ConspectusGraphitic carbon nitride-based materials have emerged as promising photocatalysts for a variety of energy and environmental applications owing to their "earth-abundant" nature, structural versatility, tunable electronic and optical properties, and chemical stability. Optimizing carbon nitride's physicochemical properties encompasses a variety of approaches, including the regulation of inherent structural defects, morphology control, heterostructure construction, and heteroatom and metal-atom doping. These strategies are pivotal in ultimately enhancing their photocatalytic activities. Previous reviews with extensive examples have mainly focused on the synthesis, modification, and application of carbon nitride-based materials in photocatalysis. However, there has been a lack of straightforward and in-depth discussion to understand the electronic characteristics and functions of various engineered carbon nitrides as well as their precise tailoring strategies and ultimately to explain the regularity and specificity of their improved performance in targeted photocatalytic systems. In the past ten years, our group has conducted extensive investigations on carbon nitride-based materials and their application in photocatalysis. These studies demonstrate the close yet intricate relationship between the electronic structure of carbon nitride materials and their photocatalytic reactivity. Understanding the electronic structure and functions of carbon nitride, as well as different engineering strategies, is essential for the improvement of photocatalytic processes from fundamental study to practical applications.To this end, in this Account, we first delve into the nature of the electronic properties of carbon nitride, highlighting the electronic structures, including band structure, density of states, molecular orbitals, and band center, as well as its electronic functions, such as the charge distribution, internal electric field, and external electric force. Subsequently, based on recent research in our group, we present a detailed discussion of the strategic modifications of carbon nitride and the consequential impacts on the physicochemical properties, particularly the optical properties and intrinsic electronic characteristics, for enhancing the photocatalytic performance. These modifications are categorized as follows: (i) component changing, which involves intralayer and interface heterojunctions as well as homojunctions, to modulate the band-edge potentials and reactivity of photoinduced electrons and holes toward surface redox reactions; (ii) dimensional tuning, which engineers the dimensional structure of carbon nitride, to influence the electron transfer direction; (iii) defect and heteroatom modification, which introduces a symmetry break in the carbon nitride framework, to promote charge redistribution for altering the charge density and electronic structure; and (iv) anchoring of single-atom metals to facilitate orbital hybridization and charge transfer enhancement through the unique metal-N coordination configurations. Finally, we propose an appraisal of the prospects and challenges in the precise manipulation and characterization of the electronic structure and functions of carbon nitride. The integration of in situ electronic structure analysis, theoretical calculation based on machine learning, and precise mechanism study may propel its substantial development in the light-driven circular economy. We hope this Account aspires to offer novel insights and perspectives into the operational mechanisms and tailored structure of carbon nitride-based materials in photocatalysis.

Progress on Copper-Based Anode Materials for Sodium-Ion Batteries.

Fossil fuels have clearly failed to meet people's growing energy needs due to their limited reserves, potential pollution of the environment, and high costs. The development of cleaner, renewable energy sources as well as secondary batteries for energy storage is imminent, in a modern society where energy demand is soaring. Sodium-ion batteries (SIBs) have become the focus of large-scale energy storage systems as a promising alternative to lithium-ion batteries. The development of SIBs relies on the construction of high performance electrode materials. The design of low cost and high performance anode materials is a key link in this regard. Copper-based anodes are characterized by high theoretical capacity, abundant reserves, low cost and environmental friendliness. A variety of copper-based anode materials, which include cobalt oxides, sulfides, selenides and phosphides, have been synthesized and evaluated in the scientific literature for sodium storage. In detail, the preparation methods, response mechanisms, strengths and weaknesses, the relationship between morphology structure and electrochemical performance are discussed, as well as highlighting strategies to improve the electrochemical performance of copper-based anode materials. Finally, we offer our perspective on the challenges and potential for the development of copper-based anodes as a means of developing practical and high performing SIBs.

Unveiling the potential of Fe2O3/TiO2 system to produce clean water: An effective and low‒cost approach for arsenic removal from ground water

The aim of this project is to estimate and eliminate arsenic by using cost‒effective approach. For the purpose, anatase TiO2 has been synthesized and sensitized with Fe2O3 using hydrothermal approach. As‒synthesized adsorbents namely Fe2O3/TiO2 were employed to remove the arsenic (III and V) contents in the form of arsenomolybdate complex (AMC). The structural morphologies and optical characteristics have been examined and assessed by various advance approaches like XRD, FTIR, Raman, SEM and AFM techniques. The BET, EDX and XPS techniques have confirmed the porosity, phase purity and chemical compositions. The stability of adsorbents was evaluated using thermo–gravimetric analysis. To extend the utility of adsorbents for successful implementation, various ground drinking water samples have been collected from Tehsil Jahania‒PK. For the quick removal and spectroscopic quantifications, arsenic contents were first converted to the arsenomolybdate complex (AMC) and then extracted via adsorption. Langmuir and Freundlich isotherm models were employed to evaluate and confirm the adsorption efficiencies, whereas Temkin model was employed to assure the electrostatic attraction between Fe2O3/TiO2 and AMC. Results indicate that the maximum adsorption capacity of Fe2O3/TiO2 is 130.1 mg/g. On the basis of survey reports and results, it has been concluded that this approach hold potential to replace the traditional adsorbents used for arsenic removal technologies.

Effect of 60 °C sustained temperature conditions on the mechanical properties and microstructure of alkali-activated fly ash-slag pastes and mortars

The temperature effect has been proven to affect the mechanical properties and microstructure of alkali-activated materials greatly. The research on the long-term complex high-temperature environment for alkali-activated materials remains blank. In this paper, the actual working temperature is selected to study the effects of long-term exposure at 60 °C on the mechanical properties of static/impact load, quality, shrinkage deformation, hydration products, pore structure, and microscopic morphology of alkali-activated fly ash-slag (AAFS). The results show that the mass loss rate of AAFS tends to be stable, the shrinkage deformation rate decreases, and the compressive strength decreases after 28d of sustained high-temperature action. The sustained high temperature causes changes in the hydration product phase, mean chain length (MCL) of the gel phase, pore structure, and micro-morphology. When the duration for 7d and 28d at 60 °C temperature, the compressive strength under static and impact loads increases, which is related to the increase of diffraction peak and MCL of the gel phase; when the duration is 60d and 90d, the compressive strength under static/impact loads decreases, which is related to the increase of cumulative pore volume and the decrease of MCL. Sustained high temperature refines the pore diameter of AAFS samples.

Investigation of the macro performance and mechanism of biochar modified ultra-high performance concrete

Ultra-high performance concrete (UHPC), an extraordinary category of cementitious composites, showcases unparalleled mechanical and durability properties. Given the current disparity in carbon levels and the environmental hazards associated with cement production, various types of biochar materials have been incorporated into cement composites. This approach offers a mutually advantageous solution, effectively reducing CO2 emissions while simultaneously preserving natural resources. This study aims to evaluate the use of palm shells, a waste biomass, as a substitute for aggregate in the UHPC matrix. The investigation focused on replacing 1–40 % of sand, specifically considering apricot, date, and peach shells biochar at an 8 % replacement. A comprehensive analysis was carried out on a total of 12 combinations, encompassing a control group. For biochar-mortar admixtures, a decrease in workability and density were observed. Replacing 1 % of sand with biochar in UHPC mortar improved compressive strength, but increasing biochar dosage weakened it. Biochar-mortar was demonstrated a dual impact on drying shrinkage. Mixtures with higher biochar dosages showed a slight increase in permeability. Incorporating 1 % biochar into UHPC led to a slightly lower electrical flux value. SEM images were obtained, highlighting the compact morphological structure seen in both the control and the 1 % biochar mortar. MIP test showed nearly 1.6 times increase in the 2-dimensional porosity, from 10.49 % (control) to 16.83 % for sample which had 30 % biochar. Based on the results obtained, it could be concluded that biochar possesses the capability, which enhances the properties of UHPC mortar when used as a partial replacement for conventional fine aggregate in minor fractions.

Chromium adsorption efficiency by functional polymeric nanocomposite membrane: A case study for environmental sustainability

AbstractWe have designed and developed nonwoven fabric supported electrospun polymeric nanofibrous‐based membrane for robust filtration system for ecological sustainability of clean water. The fabricated nanocomposites filters were tested for the removal of chromium (VI) toxic heavy metal ions from contaminated feedstock water. The interpenetrating network like morphological structure obtained from pure and composite nanofibers‐based membranes have been thoroughly investigated to understand the structure–properties of highly entangled system. It has been found that incorporating functional moieties onto nanocomposite membranes significantly impacts the absorption efficiency of toxic metals. The pore sizes of the hierarchical geometries have been varied to insight into its impact on flow rate and efficiency of filtration. The strategy of interfacing the multifunctional composite polyethylene terephthalate nanofiber membrane supported on nonwoven fabric to generate heterostructures has found to provide mechanically stable platform for efficient metal ion removal. It has been found by BET surface area analysis that the nanofibers reinforced with functional nanomaterials has controlled pore geometry compared to pristine PET electrospun nanofibers which lead to higher absorption of metal ions. We have highlighted the importance of mechanically stable electrospun polymeric nanofibers membrane‐based mitigation strategies to meet the huge demand of potable water for long‐term environmental sustainability.Highlights Mechanically toughened freestanding nanofibers mat supported on nonwoven fabric. Functionally upgrade nanofibers by incorporation of carbon based nanofillers. Controlled porosity by morphological optimization for removal of contaminates.

Ferulic acid-g-tamarind gum/guar gum based in situ gel-forming powders as wound dressings

The current research endeavour aimed to synthesize ferulic acid grafted tamarind gum/guar gum (FA-g-TG/GG) based powders as wound dressings, which could form in situ gels upon contact with wound exudates. In this context, variable amounts of FA were initially grafted with TG via the Steglich esterification reaction protocol and the resulting conjugates were subsequently amalgamated with GG and lyophilized to produce dry powders (F-1 – –F-3) with average particle size within 5.10–5.54 μm and average angle of repose ∼30°. These powders were structurally characterized with 1H NMR, FTIR, DSC, TGA, XRD and SEM analyses. Pristine TG, FA-g-TG and FA-g-TG/GG powders (F-2) revealed their distinct morphological structures and variable negative zeta potential values (−11.06 mV–25.50 mV). Among various formulation (F-1–F-3), F-2 demonstrated an acceptable powder-to-gel conversion time (within 20 min), suitable water vapour transmission rates (WVTR, 2564.94 ± 32.47 g/m2/day) and excellent water retention abilities and swelling profiles (4559.00 ± 41.57 %) in wound fluid. The powders were cytocompatible and conferred antioxidant activities. The powders also displayed fibroblast cell proliferation, migration and adhesion properties, implying their wound-healing potentials. Thus, the developed in situ gel-forming powders could be employed as promising dressings for wound management.

Effect of magnesia additive on the morphology and physico‐mechanical properties of kaolinitic clays ceramics

AbstractNigeria is rich in various minerals, including crude oil and solid minerals. However, despite this abundance, effectively utilizing these resources remains a challenge. Kaolin, also known as white China clay, is a crucial raw material used in industries such as ceramics, paper, paint, plastic, and welding electrodes. Despite its plentiful availability in Nigeria, kaolin has not been adequately exploited. Consequently, Nigeria spends approximately 14.35 million USD annually to import refined kaolin to meet local demand, due to the lack of capacity to process it to the required industrial standards. This study investigates the effect of magnesia (MgO) on the morphology and physico‐mechanical properties of kaolinitic clay ceramics using the slip‐casting method. Various analytical techniques were employed to examine the kaolin, including X‐ray fluorescence (XRF), X‐ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier Transform Infrared Spectroscopy (FTIR), and Scanning Electron Microscopy (SEM). Also, compressive and flexural tests were conducted. The XRF analysis revealed that all samples contained SiO2 (54.41%wt), Al2O3 (34.05%wt), and other trace elements. The main mineral phases identified were quartz, microcline, and orthoclase. Among the samples, 30–200 exhibited the highest compressive strength at 218 MPa, while the highest flexural rigidity was observed in sample 15–200. The results indicated that MgO significantly affected the properties of kaolin, as the control sample had a compressive strength of 59 MPa. The study also found that the quantities of additives should align with stoichiometric requirements. Results showed hypo‐stoichiometry in samples 30–600 and 15–400, and hyper‐stoichiometry in sample 60–200. XRF, XRD, and FTIR spectra confirmed the elemental and chemical compositions of the samples, while SEM analysis revealed the morphological structure. It was observed that increasing the magnesia content from 10% to 30% led to an increase in pore spaces within the samples. TGA analysis provided insights into the relationship between mass loss and temperature variation in the ceramic samples, While The DTG curves explain the endothermic phase changes over changes in temperature; at 50–150°C, loss of the water phase is complete, at 300–400°C burning of organic matter phase is achieved and at 500–700°C endothermic dihyroxylation phase begins forming armorphous meta‐kaolin.

Molecular Composition of Humic Acids and Soil Organic Matter Stabilization Rate of the First Arctic Carbon Measurement Supersite “Seven Larches”

In the framework of the implementation of the all-Russian climatic project “Carbon measurement test sites”, reference soils of “Seven Larches” carbon supersite, which is a benchmark and the only monitoring site in the Artistic latitudes, were investigated. The morphological structure of representative soils was specified, and it was found that soils are classified as Cryosols of different types (Histic, Stagnic or Gleyic). The basic physico-chemical characteristics of the soils were studied. By means of elemental analysis and 13C NMR spectroscopy, the composition and molecular structure of humic acids from organic and mineral soil horizons were studied. The surface (organic) soil horizons are characterized by high values of H:C molar ratios (1.2–1.3), which indicates a lower degree of the molecular structure aromaticity of humic acids from organic soil horizons. Analysis of the molecular structure of humic acids by 13C NMR spectroscopy showed that humic acids of the studied soils are characterized by the predominance of non-substituted aliphatic (0–47 ppm) and aromatic (108–164 ppm) fragments. Mineral soil horizons are characterized by higher stabilization of organic matter (with lower SOC content—0.5–0.9%) and higher hydrophobicity of humic acid molecules. Comparison of the obtained results with previously published data on the structural and elemental composition of humic acids isolated from soils of similar genesis and geographical location did not reveal any significant differences between the data obtained by us and previously published data. Thus, for “Seven Larches” carbon supersite “reference” parameters of elemental composition of humic acids, their molecular composition and degree of stabilization of soil organic matter were identified.

Classification, density, and spatial distribution of polychaete reefs in the Coorong, South Australia

The cosmopolitan species Ficopomatus enigmaticus is one of the most prominent providers of polychaete reefs in shallow and brackish waters. The effects of polychaete reefs on the environment can be positive or negative subject to their structural complexity and vary with local environmental conditions and over time. The Coorong is a large temperate estuarine and lagoonal system with extensive polychaete reefs built by F. enigmaticus. The aims of this study were to (1) classify polychaete reefs based on size and morphology, (2) quantify reef density, (3) assess their spatial distribution and (4) assess the correlation between reefs (e.g., density, size) with the environmental gradient. Structural morphologies of F. enigmaticus were classified as either halo, circular, irregular, platform or fringing reef types. The largest densities of polychaete reefs were recorded in the vicinity of the mouth of the estuary with 224 reefs per ha compared to the lagoon (62 reefs per ha). The most common reef morphology was circular and largest sizes in the lagoon were positively correlated with salinity, chlorophyll a, TRIX (trophic index) and bicarbonate. The largest reef diameter recorded was 11.3 m, exceeding previously known F. enigmaticus circular reef formations globally. The growth of large circular reefs may have benefitted from low flows and eutrophic conditions in the Coorong during the last two decades. This study serves as an important baseline for future assessments of reef change in a Ramsar listed wetland. Furthermore, this study highlights reef characteristics of F. enigmaticus across an environmental gradient, which can be informative for the management of flow and eutrophication in estuaries and coastal lagoons.

Experimental and numerical investigation of heat sinks constructed by anisotropic 3-D Turing patterns

Heat dissipation is a critical issue for various engineering applications such as electronic devices, turbine blades and batteries. Existing heat sink structures contained inherent shortages in geometric flexibility which prevented further development of heat dissipation technologies. This study proposed a self-organized design method for heat sinks inspired by Turing Patterns (TP) in nature morphogenesis. The biomimetic structures were parametrically controlled with the aid of reaction-diffusion equations in terms of feature size, feature density, structural morphology and structural orientation. The metallic selective laser melting (SLM) technology was adopted to fabricate the three-dimensional (3-D) heat sinks. Experimental and numerical evaluations were conducted to compare TP structures with traditional pin-fin (PF) arrays baselines. Results showed substantial advantages of the TP structures in regulating flow field and enhancing height-wise fluid mixing. The thermal performance factor (TPF) of TP structures is approximately 45 % higher than traditional PF structures with similar feature sizes. The globally averaged magnitude of height-wise velocities of TP structure is around 2.4 times larger than that of PF structures due to the existence of the threshold-like and bridge-like structures. With the aid of three-dimensional structures, full utilization of the coolant was achieved to further increase the heat transfer intensity, while a high synergic level was formed within the flow field and temperature field to reduce the pressure drop. The design method proposed in this study demonstrated strong capability in tuning three-dimensional flow field and is expected to provide new insights to the heat transfer area that faces nonuniform thermal conditions and inhomogeneous flow conditions.

Beyond head and wings: Unveiling influence of diet, body size, and phylogeny on the evolution of the femur in phyllostomid bats.

Phyllostomidae, the most diverse family of Neotropical bats, encompass 230 species with varied dietary habits and food acquisition methods. Their feeding niche diversification has shaped skull and wing morphologies through natural selection, reflecting food processing and flight strategies. Yet, evolution of bat hindlimbs, especially in phyllostomids, remains little understood. Previous studies highlighted the femur's morphology as a key to understanding the evolution of quadrupedalism in yangochiropteran bats, including the adept walking observed in vampire bats (Desmodontinae). Here, we aimed to describe the femoral morphological variation in Phyllostomidae, correlating this with body size and assessing the effects of phylogenetic history, dietary habits, and hindlimb usage. Analyzing 15 femoral traits from 45 species across 9 subfamilies through phylogenetically informed methods, we discovered a significant phylogenetic structure in femoral morphology. Allometric analysis indicated that body mass accounts for about 85% of the variance in phyllostomid femoral size and about 11% in femoral shape. Relatively smaller femurs showed to be typical in Stenodermatinae, Lonchophyllinae, and Glossophaginae, in contrast to the larger femurs of Phyllostominae, Desmodontinae, Micronycterinae, and Lonchorrhininae. Furthermore, extensive femur shape variation was detected, with the most distinct morphologies in vampire bats, followed by frugivorous species. Adaptive evolutionary models related to diet more effectively explained variations in femoral relative size and shape than stochastic models. Contrary to the conventional belief of limited functional demand on bat femurs, our findings suggest that femoral morphology is significantly influenced by functional demands associated with diet and food capture, in addition to being partially structured by body size and shared evolutionary history.

Biomimetic design and integrated biofabrication of an in-vitro three-dimensional multi-scale multilayer cortical model

The lack of accurate and reliable in vitro brain models hinders the development of brain science and research on brain diseases. Owing to the complex structure of the brain tissue and its highly nonlinear characteristics, the construction of brain-like in vitro tissue models remains one of the most challenging research fields in the construction of living tissues. This study proposes a multi-scale design of a brain-like model with a biomimetic cortical structure, which includes the macroscopic structural features of six layers of different cellular components, as well as micrometer-scale continuous fiber structures running through all layers vertically. To achieve integrated biomanufacturing of such a complex multi-scale brain-like model, a multi-material composite printing/culturing integrated bioprinting platform was developed in-house by integrating cell-laden hydrogel ink direct writing printing and electrohydrodynamic fiber 3D printing technologies. Through integrated bioprinting, multi-scale models with different cellular components and fiber structural parameters were prepared to study the effects of macroscopic and microscopic structural features on the directionality of neural cells, as well as the interaction between glial cells and neurons within the tissue model in a three-dimensional manner. The results revealed that the manufactured in vitro biomimetic cortical model achieved morphological connections between the layers of neurons, reflecting the structure and cellular morphology of the natural cortex. Micrometer-scale (10 μm) cross-layer fibers effectively guided and controlled the extension length and direction of the neurites of surrounding neural cells but had no significant effect on the migration of neurons. In contrast, glial cells significantly promoted the migration of surrounding PC12 cells towards the glial layer but did not contribute to the extension of neurites. This study provides a basis for the design and manufacture of accurate brain-like models for the functionalization of neuronal tissues.

MHD lensing in inhomogeneous ISM for qualitative understanding of the morphology of supernova remnants

Morphological evolution of expanding shells of fast-mode magnetohydrodynamic (MHD) waves through an inhomogeneous ISM is investigated in order to qualitatively understand the complicated morphology of shell-type supernova remnants (SNR). Interstellar clouds with high Alfvén velocity act as concave lenses to diverge the MHD waves, while those with slow Alfvén velocity act as convex lenses to converge the waves to the focal points. By combination of various types of clouds and fluctuations with different Alfvén velocities, sizes, or wavelengths, the MHD-wave shells attain various morphological structures, exhibiting filaments, arcs, loops, holes, and focal strings, mimicking old and deformed SNRs.

The morphology of the pygidial glands and the chemical composition of their secretions of four sphodrine ground beetle species (Carabidae: Platyninae)

Ground beetles possess a pair of pygidial glands that produce and release secretions that play an important role in defense against predators. The morphology of these glands and the chemical composition of their products were studied in four species of the tribe Sphodrini: Calathus (Calathus) fuscipes (Goeze, 1777), C. (Neocalathus) cinctus Motschulsky, 1850, C. (N.) melanocephalus (Linnaeus, 1758) and Laemostenus (Antisphodrus) elongatus (Dejean, 1828). The morphological analyzes of the glands of the four taxa mentioned were carried out for the first time using bright-field and nonlinear microscopy. All morphological structures were precisely measured and photographed. The pygidial gland secretions of C. (C.) fuscipes and L. (A.) elongatus were analyzed for the first time using gas chromatography-mass spectrometry. A total of 30 compounds were detected from the extracts of pygidial gland secretions of the four Sphodrini species studied. The simplest chemical mixture was found in L. (A.) elongatus, while the most complex secretion was that of C. (C.) fuscipes. 1-Undecanol, which we were able to detect in all taxa examined here, and dodecyl butyrate, which was detected in the three Calathus species, have never before been detected in the secretions of ground beetles.

The role of carboxylic acid contents in calcium-based metal-organic frameworks for the enhancement of Biginelli reaction

Metal-organic frameworks (MOFs) can carry different functional groups such as COOH, NH2, and SO3H. The most commonly used functional group was COOH due to its Brønsted acidity, polarity, and ability to bond with organic compounds and metals through various interactions. Here, calcium-based MOFs (Ca-MOFs) with different carboxylic arms were successfully prepared and used in heterogeneous Biginelli catalytic reactions. The prepared materials (Ca-BDC-H, Ca-BDC-COOH, and Ca-BDC-(COOH)2) were characterized using different spectroscopic techniques and the morphological structures were determined using microscopic analysis. Besides elucidating the fine form of MOFs, the role of the carboxylic content was tested in multicomponent reaction catalysis in different kinetics and thermodynamic studies, the formation of catalytic products was determined using NMR analysis, and the proposed mechanism was investigated. The results obtained showed that as the carboxylic content in the network increases, the catalytic reaction yield increases which can support the possibility of using the COOH group present in the network with acidic properties in heterogeneous catalysts giving high product yield.

Synthesis of CS/Fe3O4/TiO2@MXene nanocomposite photocatalyst with excellent degradation and bacteriostatic properties by one-step hydrothermal method

With the rapid development of global economy and industrialization, the management and protection of water resources have become increasingly important. In this paper, a novel three-dimensional Chitosan/Fe3O4/TiO2@MXene photocatalyst with excellent degradation and bacterial inhibition properties was prepared by a simple one-step hydrothermal method using FeCl3·6H2O, Chitosan (CS) and MXene (Ti3C2) as main raw materials. TiO2 was generated in-situ on the surface of Ti3C2 nanosheets and modified by loading Fe3O4 nanoparticles and CS films. The conformations and band gaps of the composites were modified, and then photocatalytic mechanisms, phase compositions, morphological structures, magnetic properties and photoelectrochemical properties of the photocatalysts were systematically analysed. The degradation efficiency of the CS/Fe3O4/TiO2@Ti3C2 composite photocatalyst can reach 95.9% when the ration of CS to FeCl3·6H2O is 1:3 and the hydrothermal temperature is 180°C, which showing excellent photocatalytic performance. Meanwhile, the inhibition rate of Staphylococcus aureus (S. aureus) is close to 98.91% under the light condition. This study further reveals that visible light is a cost-effective way to treat pollutions in terms of degradation and bacteriostatic inhibition, and the composite photocatalysts can be efficiently recycled and reused under the action of a magnetic field.

Chromoionophoric molecular probe infused bimodal porous polymer rostrum as solid-state ocular sensor for the selective and expeditious optical sensing of ultra-trace toxic mercury ions

This study presents a distinctive solid-state naked-eye colorimetric sensing approach by encapsulating a chromoionophoric probe onto a hybrid macro-/meso-pore polymer scaffold for fast and selective sensing of ultra-trace Hg(II). The customized structural/surface properties of the poly(VPy-co-TM) monolith are attained by specific proportions of 2-vinylpyridine (VPy), trimethylolpropane trimethacrylate (TM), and pore-tuning solvents. The interconnected porous network of poly(VPy-co-TM), inherent superior surface area and porosity, is captivating for the homogeneous/voluminous incorporation of probe molecules, i.e., 7-((4-methoxyphenyl)diazenyl)quinoline-8-ol (MPDQ), for the target-specific colorimetric detection. The structural morphology, surface topography, and phase characteristics of the bare poly(VPy-co-TM) monolith and MPDQ@poly(VPy-co-TM) sensor are examined using HR-TEM-SAED (High-Resolution Transmission Electron Microscopy - Selected Area Electron Diffraction), FE-SEM-EDAX (Field Emission Scanning Electron Microscopy - Energy Dispersive X-ray Spectroscopy), XPS (X-ray Photoelectron Spectroscopy), p-XRD (Powder X-Ray Diffraction), FT-IR (Fourier Transform Infrared Spectroscopy), UV-Vis-DRS (Ultraviolet-Visible Diffuse Reflectance Spectroscopy), and BET/BJH (Brunauer-Emmett-Teller / Barrett-Joyner-Halenda) analysis. The distinctive properties of the sensor reveal a constrained geometrical orientation of the MPDQ probe onto the long-range continuous monolithic network of meso-/-macropore template, enabling selective interaction with Hg(II) with peculiar color transfiguration from pale yellow to deep brown. The sensor demonstrates a linear spectral-color alliance in the 0–200 ppb concentration range for Hg(II), with quantification and detection limits of 0.63 and 0.19 ppb. The sensor efficacy is verified using certified contaminated water and tobacco samples, with excellent reusability, reliability, and reproducibility of ≥ 99.23 % (RSD ≤1.89 %) and ≥ 99.19 % (RSD ≤1.94 %) of Hg(II), respectively.

Synthesis of carbon nitride nanosheets with N vacancies boosted by S doping for photocatalytic efficient killing of E. coli under visible light

To address the problem of bacterial contamination in drinking water, we synthesized non-metallic photocatalysts for the inactivation of Escherichia coli in drinking water. In this paper, S-g-C3N4 (S-g-CN) composite nanomaterials were synthesized via a one-step calcination method. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance (EPR), and transmission electron microscopy (TEM) analyses confirmed the successful synthesis of S-g-CN with N vacancies. Scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) spectroscopy analyzed the layered morphology and chemical structure of g-C3N4 before and after modification. Optical characterization revealed significantly enhanced light absorption, electron-hole separation efficiency, and carrier mobility in the modified samples. Bactericidal assays demonstrated that under visible light, 0.3 % S-g-CN nanomaterials exhibited superior bactericidal effects against E. coli compared to unmodified g-C3N4. Furthermore, 0.3 % S-g-CN demonstrated excellent degradation of Rhodamine B (RhB) under various conditions (pollutant concentration, pH, and catalyst dosage). Recyclability studies over three cycles confirmed the catalyst's stability and reusability.