SEM Micrographs Research Articles

A sustainable green-approach for biofabrication of chitosan nanoparticles, optimization, characterization, its antifungal activity against phytopathogenic Fusarium culmorum and antitumor activity.

Chitosan is a natural non-toxic, biocompatible, biodegradable, and mucoadhesive polymer. It also has a broad spectrum of applications such as agriculture, medical fields, cosmetics and food industries. In this investigation, chitosan nanoparticles were produced by an aqueous extract of Cympopogon citratus leaves as a reducing agent. According to the SEM and TEM micrographs, CNPs had a spherical shape, and size ranging from 8.08 to 12.01 nm. CNPs have a positively charged surface with a Zeta potential of + 26mV. The crystalline feature of CNPs is determined by X-ray diffraction. There are many functional groups, including C꞊C, CH2-OH, C-O, C-S, N-H, CN, CH and OH were detected by FTIR analysis. As shown by the thermogravimetric study, CNPs have a high thermal stability. For the optimization of the green synthesis of CNPs, a Face centered central composite design (FCCCD) with 30 trials was used. The maximum yield of CNPs (13.99 mg CNPs/mL) was produced with chitosan concentration 1.5%, pH 4.5 at 40°C, and incubation period of 30 min. The antifungal activity of CNPs was evaluated against phytopathogenic fungus; Fusarium culmorum. A 100% rate of mycelial growth inhibition was gained by the application of 20mg CNPs/mL. The antitumor activity of the green synthesized CNPs was examined using 6 different cell lines, the viability of the cells reduced when the concentration of green synthesized CNPs increased, the IC50 dose of the green synthesized CNPs on the examined cell lines HePG-2, MCF-7, HCT-116, PC-3, Hela and WI-38 was 36.25 ± 2.3, 31.21 ± 2.2, 67.45 ± 3.5, 56.30 ± 3.3, 44.62 ± 2.6 and 74.90 ± 3.8; respectively.

Centrifuge modeling of levees with geocomposite chimney drain subjected to flooding

The objective of the present study is to evaluate the performance of a levee section when subjected to flooding and subsequent seepage through centrifuge model tests. For this, six centrifuge model tests were conducted on a 240 mm high levee model at 30g in a 4.5 m radius large beam geotechnical centrifuge available at the Indian Institute of Technology Bombay, India. A custom-developed flooding simulator is employed to induce identical flood rates on the upstream side of the levee models. Further, using (a) geocomposite (GC) and (b) sand-sandwiched geocomposite (SSGC) as internal chimney drain, the suitability of GC material for dissipation of pore-water pressure (PWP) is also studied. The results of the centrifuge tests are presented and discussed in terms of the development of upstream flood function, subsequent PWP development within the levee body, and the surface settlements observed at the levee's crest. Further, the influence of an internal chimney drain, the material used for its construction, and its type and composition on the seepage response of the levee is discussed in detail. The performance GC chimney drain placed within the levee section subjected to flooding-induced seepage is compared with a conventional sand chimney drain. It is observed that a GC-based chimney drain with sand cushioning on both sides in the horizontal portion of the chimney drain performs well. Further, digital image analysis of SEM micrographs of exhumed GC after centrifuge tests and the analyzed PWP data during sustained flooding-induced seepage is found to corroborate well.

Field-assisted sintering of high-entropy alloy-reinforced aluminium matrix composites: phase identification and microstructural properties

AbstractThis study investigates the design, phase identification, and microstructural properties of high-entropy alloy (HEA)-reinforced aluminium (Al) matrix composites. Thermophysical expressions for HEAs were employed during the design phase of the HEA; both theoretical frameworks and experimental analyses were used to anticipate stable phases while a field-assisted sintering technique was employed to consolidate the samples. Calculation of phase diagram (CALPHAD) predictions for the phases present in the HEA align with valence electron concentration (VEC) calculations as both predicted the presence of BCC and FCC phases. The microhardness results reveal a substantial increase in the hardness value of the composites as compared to the pure Al, such that as low as 5 wt% HEA addition resulted in over a 100% improvement, while the densification of the composites was found to decrease with an increase in the wt% of HEA. SEM micrographs and XRD analyses show fair dispersion, bonding, and phase integration in the HEA-reinforced composites.

Effect of high-pressure treatment and germination on the functional, rheological, and microstructural characteristics of red quinoa (Chenopodium quinoa) gels

This study investigates the effect of germination and high-pressure (HP) treatment on the functional and gelling behaviour of red quinoa (RQ) (Chenopodium quinoa). The grains were subjected to germination for 48 h followed by the application of four pressures (200, 300, 400 and 500 MPa) as well as their combinations to germinated quinoa (GQ) samples. The samples were ground, and the flour was analysed for functional, rheological, and microstructural attributes. Germination and HP treatment improved the functional and gelling properties of RQ samples significantly. The degradation of protein, fat, and starch-lipid complex of the flour led to an increase in the swelling capacity of flour. The treatments increased the oil absorption capacity from 50.02 ± 0.47 to 80.86 ± 0.88 % and emulsification capacity from 57.85 ± 0.71 to 64.17 ± 0.53 %. This increase is attributed to the dissociation and unfolding of polypeptides that expose the hydrophobic sites of amino acids. The decrease in least gelling capacity from 18 to 14% signified a decrease in the amount of flour required for the gelation. Rheometric and texture profile analysis demonstrated an improved gel strength. Moreover, the SEM micrographs showed an increased structure density and reduced porosity which further support the improved gel strength. The study would help to widen the scope of accommodating RQ flour as a gelling or thickening agent in the food industries.

Radical scavenging potential of spectrophotometric, spectroscopic, microscopic, and EDX observed zinc oxide nanoparticles from leaves, buds, and flowers extract of Bauhinia Variegata Linn: A thorough comparative insight.

The present study incorporated an environment-friendly and cost-efficient green synthesis method for fabricating zinc oxide nanoparticles (ZnO-NPs) using various parts (leaves, buds, and flowers) of Bauhinia Variegate Linn. UV-Spectrophotometric analysis was used to confirm the synthesis of ZnO-NPs, which showed an absorption band within 360-380 nm range. Further techniques like FT-IR spectroscopy and (SEM) scanning electron microscopy equipped with a novel EDX were also included to confirm the synthesis, size, and shape of ZnO-NPs. Results obtained by FT-IR showed that the phytochemicals present in the ethanolic extract successfully acted as a capping agent. SEM micrographs confirmed irregularly shaped nanoparticles with an average size of 70-80 nm. The presence of Zinc and Oxygen peaks in EDX also confirmed the successful synthesis of ZnO nanoparticles. The radical scavenging (antioxidant) potential of prepared nanoparticles was also evaluated by DPPH radical assay. The ZnO-NPs obtained from the ethanolic extract of buds showed the highest %RSA (86%) as compared to the flowers (79%) and leaves (76%). The current study findings showed the versatile morphology of all parts of the plant with significant antioxidant potential, establishing the use of Bauhinia Variegate in biological systems for various biomedical applications. RESEARCH HIGHLIGHTS: A thorough comparative analysis of the radical scavenging power of major parts of the Bauhinia Variegate, which is 1st of its kind. Extensive characterization using UV-Vis spectrophotometry, FT-IR, SEM, and EDX to observe the conformational and morphological changes. Analysis of the reduction potential of leaves, buds, and flowers of a single plant for future directions in green synthesis.

Low-Cycle Fatigue Behavior and the Combined Cyclic Hardening Material Model of Plate-Shaped Zn-22Al Alloy for Seismic Dampers.

This study investigates the potential of the plate-shaped Zn-22 wt.% Al (Zn-22Al) alloy as an innovative energy dissipation material for seismic damping devices, since plate-shaped material is more suitable to fabricate large-scale devices for building structures. The research begins with the synthesis of Zn-22Al alloy, given its unavailability in the commercial market. Monotonic tensile tests and low-cycle fatigue tests are performed to analyze material properties and fatigue performance of plate-shaped specimens. Monotonic tensile curves and cyclic stress-strain curves, along with SEM micrographs for microstructure and fracture surface analysis, are acquired. The combined cyclic hardening material model is calibrated to facilitate finite element analysis. Experimental results reveal exceptional ductility in Zn-22Al alloy, achieving a fracture strain of 200.37% (1.11 fracture strain). Fatigue life ranges from 1126 to 189 cycles with increasing strain amplitude (±0.8% to ±2.5%), surpassing mild steel by at least 6 times. The cyclic strain-life relationships align well with the Basquin-Coffin-Manson relationship. The combined kinematic/isotropic hardening model in ABAQUS accurately predicts the hysteretic behavior of the material, showcasing the promising potential of Zn-22Al alloy for seismic damping applications.

Enhancing sp3 content in diamond-like carbon thin film electrodes by pulsed laser annealing for durable charge storage performance

In this work, diamond-like carbon (DLC) thin film electrodes were grown on Si substrate by pulsed laser deposition (PLD) technique, and the implication of pulsed laser annealing (PLA) treatment on their electrochemical supercapacitor performance was examined by three electrode systems in 1 M Na2SO4 electrolyte solutions. The SEM micrographs exhibit a sheet-like wrinkled surface of DLC film on Si which later transformed into tiny hierarchical heap-like structures with enhanced surface roughness. The Raman spectra confirm signature of the D and G peaks of pristine DLC film at ~1352 cm−1 (1356 cm−1 after PLA) and 1591 cm−1 (1589 cm−1 after PLA), and appearance of minor T2g (diamond) (1332 cm−1) peaks with an increment of the sp3 content after PLA treatment. The X-ray photoelectron spectroscopy (XPS) spectra were deconvoluted into three different contributions CC (sp2), CC (sp3), and CO, and their sp3 percentages were estimated ~48.9 %, and 64.7 % before and after annealing. The area under cyclic voltammetry (CV) curve and galvanostatic charging discharging (GCD) performance of PLA-treated DLC film were improved and the highest areal-specific capacitance was obtained to be ~48.25 mF/cm2 for scan rate of 5 mV/s and 36.01 mF/cm2 for current density of 2 mA/cm2, respectively. Excellent charging discharging cyclic stability of PLA treated electrode was observed over 5000 cycles, and Coulombic efficiency and capacitance retention were determined to be ~93.5 % and ~ 97.3 %, respectively. The electrochemical impedance spectroscopy (EIS) was performed to obtain the Nyquist plot (Z′vs.Z′′) of both electrodes before and after the stability test, and a small degradation in impedance was observed. The Nyquist plots were fitted with the well-known Randles equivalent circuit model Rs(Cdl(RctZw)) and substantial curtailment of Warburg resistance (Zw) in PLA-induced DLC electrode signifies the dominance of the diffusion-controlled region in the charging-discharging process. Minor changes in the Nyquist plot before and after the stability test manifest the enduring charge kinetics of both electrodes and PLA-treated DLC exhibits better cyclic stability. PLA techniques have a great impact on upgrading the areal-specific capacitance, capacitance retention with high Coulombic efficiency, and stability with negligible impedance loss of the DLC film electrodes.

Novel synthesis of trans-ferulic acid loaded tragacanth-chitosan nanoformulations and evaluation of their biological activities

Trans-ferulic acid, is one of the many biologically significant bioactive components of Datura. It has wide range of potential applications in the food industry, health, and cosmetics industries. Trans-ferulic acid possess myriad properties like anti-inflammatory, anti-aging, antiangiogenic, anticancer, antimicrobial, and antioxidant properties. To exploit its antioxidant and anti-inflammatory properties, first of all, trans-ferulic acid loaded tragacanth/chitosan nanoparticles (TFA loaded TGCA-NPs) were synthesized by ionic gelation method using tragacanth and chitosan as polymers. Tragacanth used to encapsulate the trans-ferulic acid is a polysaccharide gum, which is used all over the world in industries ranging from the food industry to healthcare systems due to its availability, affordability, non-toxicity, and environmental friendliness. The synthesized nanoparticles were then characterized by using techniques like FTIR, UV–Vis Spectroscopy, SEM and TEM. The particle size of nanoparticles thus obtained ranged from 105 nm to 250 nm. SEM micrograph of nanoparticles showed tiny rod-like structures, which appear to be coated on the polymer. TEM images showed somewhat sphere-shaped nanoparticles with a projecting rod-like structure that might be due to the trans-ferulic acid encapsulation in tragacanth-chitosan polymer. Decent antimicrobial activity of synthesized nanoparticles was observed against pathogenic bacteria named Staphylococcus aureus. Hemocompatibility of trans-ferulic acid loaded tragacanth-chitosan nanoparticles was also examined. The antioxidant activity was evaluated by DPPH radical scavenging assay, in which synthesized nanoparticles showed 41.62 % radical scavenging activity. For in-vitro anti-inflammatory activity Human Red Blood Cell membrane stabilization method (HRBC method) was used, and the results showed higher protection by the synthesized nanoparticles in comparison to the pure trans-ferulic acid and blank nanoparticles.

Durability and ecological assessment of low-carbon high-strength concrete with short AR-glass fibers: Effects of high-volume of solid waste materials

The goal of this research is to improve the mechanical characteristics and durability of concrete while adhering to green and sustainable development principles. Portland cement (PC) was replaced with ceramic waste powder (CWP), glass powder (GP), and granite waste powder (GWP) to create the low-carbon, high-strength concrete (HSC). These materials were incorporated at 0–50% as a partial replacement of PC. The short alkali-resistant (AR-) glass fiber content was added by 1.0% of the PC content. The changes in strength, microstructure, pore structure, as well as ecological assessment of HSCs was investigated. Various experiments on the durability properties and elevated temperature resistance of HSC were performed. The experimental results show that mechanical properties of HSC with 10%GP and 20%GWP were maximally enhanced at 28d, while the mechanical properties of HSC with 50% of all wastes are decreased. It was found also that HSC containing CWP showed significant reductions in carbonation depth (up to 65.89% lower than the control mixture), especially at higher replacement levels. Furthermore, the increment in substitution level of CWP has found an increment in pore volume, resulting in a reduction in preliminary strength performance. It was observed that a 50% substitution level of GP and GWP reduced the water penetration depth by 47.71% and 65.7% compared to the control mixture, respectively. The residual strength after 600 °C exposure for 10%CWP, 10% GP, and 20% GWP retained about 34.10%, 32.32%, and 43.29%, respectively, from their original strength. XRD tests and SEM micrographs showed that adding 10%GP and 20%GWP improve the hydration reactions. Finally, environmental assessments revealed that incorporating CWP, GP, and GWP into HSC led to reduced costs, energy consumption, and carbon footprint.

Investigations on the microbial activity and anti-corrosive efficiency of nickel oxide nanoparticles synthesised through green route

Abstract Researchers have shown considerable interest in the environmentally friendly synthesis of several nanoparticles particularly metal nano particles due to their multifaceted applications. The target of the current research includes the synthesis of nickel oxide nanoparticles (NiO-NPs) through the green route using the bark extract from Acacia Nilotica, and analyzed their chemical and surface morphological features using XRD, SEM, EDX, IR, UV–vis and photoluminescence spectroscopy. In addition, the corrosion inhibition ability and antimicrobial activity of the extract were also studied. The XRD analysis indicated that the NiO exist in the form of nanoparticles. It showed the formation of pure cubic NiO-NP with a prominent peak at 43.28° reflected from the plane (200). The crystallite size was found to be 15.83 nm. The SEM micrographs revealed that NiO-NPs appeared to be a bulk cluster-like structure on their surface.The EDX analysis displayed the presence of Ni and oxygen atoms. The photoluminescence spectrum demonstrated that the green synthesized metal oxide nanoparticles have a modified emission band due to the presence of oxygen deficiencies and induced surface imperfections. The Fourier transform infrared spectroscopy (FTIR) confirmed the association of peaks with the C–H and Ni–O bonds. The UV–vis study showed a maximum absorption at 264 nm. A study on the inhibition efficiency towards microbes confirmed that the prepared NiO-NPs have a good inhibition against selected microbes such as S. aureus, E. coli, Candida albicans, A. Niger. The mass loss system showed restraint 93.68 % effectiveness in the mild steel, and the electrochemical study supported the formation of a defensive protective layer on the cathodic locales of the carbon steel surface inhibiting corrosion.

The effect of filler loading, biological treatment, and bioplastic blend ratio on flexural and impact properties of blended bioplastic reinforced with spent coffee ground

AbstractIn this study, the mechanical and morphological characteristics of poly(hydroxyalkanoate) (PHA)/poly(lactic acid) (PLA) blend matrix reinforced with spent coffee ground (SCG) were investigated across various weight ratios (100/0, 75/25, 50/50, 25/75, and 0/100) and SCG contents (10–40 wt%). SEM micrographs revealed a phase‐separated structure with cracks on the fracture surface, consistent with the lower flexural properties of biocomposites. The incorporation of SCG reduced mechanical properties, mainly due to its incompatibility with the PHA/PLA matrix. Biocomposites with high SCG content demonstrated lower energy absorption capabilities, likely due to SCG aggregates acting as stress concentrators and disrupting load‐transferring mechanisms. Moreover, increasing PHA content in the blends led to higher PLA crystallinity, as PHA acted as a nucleating agent for PLA. For biological treatment, biocomposites with PHA/PLA ratio (50/50) and SCG loading (20 wt%) were employed. The microscopic analysis highlighted well‐dispersed treated SCG within the matrix and improved interfacial contact. Biocomposites with treated SCG demonstrated remarkable enhancements of 52% and 113% in flexural strength and modulus, respectively. These findings proved the effectiveness of sustainable fungal treatment in enhancing interfacial adhesion and improving the mechanical performance of biocomposites.Highlights Percentage of SCG in bioplastic blend as a significant effect on the flexural properties and impact strength. The ratio of the bioplastic blend has the strong influence on the flexural properties and impact properties. Biological treatment of SCG has improved the interfacial interaction between SCG and bioplastic blend. The treated SCG has rougher surface which facilitates the interfacial locking between bioplastic blend and treated SCG. The biological treatment of SCG has improved the mechanical properties of the composites.

Degradation of rhodamine B dye under visible and solar light on zinc oxide and nickel-doped zinc oxide thin films

The kinetic investigation of rhodamine B dye's photocatalytic degradation, chosen as a model pollutant, was conducted at room temperature using Zinc oxide (ZnO) and nickel-doped zinc oxide (Zn0.97Ni0.03O) photocatalysts synthesized through the spray pyrolysis method. XRD analysis confirmed the formation of hexagonal ZnO and Zn0.97Ni0.03O films, with crystallite sizes ranging from 19 to 29 nm and varying in mean average grain size from 72 nm to 88 nm. The surface morphology of the Ni-doped ZnO films was influenced by nickel doping, observed through SEM and TEM micrographs, revealing a dense structure of spherical-shaped crystals. Light transmission and optical band gap energy of the films ranged between specified values, ranging from 3.27 to 3.24 eV. The degradation process was assessed under various conditions, including different light sources (UV lamp and solar irradiation), pH levels, and substrate concentrations. Degradation followed a pseudo-first-order kinetic model, with rate constants (k) and half-life times (t1/2) calculated accordingly. The degradation efficiency of undoped ZnO and ZnO doped with nickel decreased with increasing concentration under UV irradiation from (0.1–0.5 M) under UV irradiation decreased from (34.29–45.02) (49.61–56.61), while under visible light are (40–45.07 %) (58.46–60.24 %), removal rates ranged within specific percentages. The porous Zn0.97Ni0.03O synthesized at 0.5 M exhibited the highest photocatalytic efficiency due to its enhanced crystallinity, resulting in degradation rates of 9.22 and 11.22 × 10−3 min−1 and half-life times of 75.18 and 61.77 min at 90 min specified for both UV and solar light irradiations, respectively. Acidification of the reaction medium accelerated the photocatalytic degradation kinetics, while alkalization slowed it down. These findings mark a significant advancement in the utilization of oxide semiconductors for water pollutant degradation under natural sunlight.

Structural, microstructural, dielectric, electrical, and magnetic properties of a scandium-modified bismuth ferrite

ABSTRACT This paper reports on the synthesis method and characterisation of a binary polycrystalline material (Pb0.6Bi0.2Sc0.2)(Fe0.4Ti0.6)O3 ceramic. The room temperature XRD pattern confirms an orthorhombic crystal structure with average crystallite size of 25.3 nm. Study on SEM micrograph reveals the homogeneous dispersal of grains and well-defined grain boundaries and also the compactness of the grains implies the development of a highly dense material. The purity and composition of this material are verified using EDX, and confirms presence of all the constituent elements (Pb, Bi, Sc, Fe, Ti, and O) both in weight and atomic percentage. According to research on dielectric spectra as a function of temperature range of 25°C to 500°C and frequency range of 1 kHz to 1 MHz, there may be Maxwell–Wagner-type dispersion at low frequencies, which considerably decreases towards higher frequencies because of decreasing space charge polarisation. The negative temperature coefficient of resistance behaviour is observed from impedance spectroscopy. The research of modulus spectroscopy demonstrates the existence of a non-Debye type of relaxation. The thermally activated charge carriers regulate the study of the conduction mechanism. The semicircular arcs found both in Nyquist and Cole–Cole plots provide an evidence for the semiconducting nature. The magnetic study reveals the superparamagnetic nature of the sample.

Encapsulation of propolis extracted with methylal in the chitosan nanoparticles and its antibacterial and cell cytotoxicity studies

In this study we develop novel type of antibacterial chitosan-propolis NPs to improve theantimicrobial activity against various pathogens. To this aim, we primarily extracted propolis with methylal and ethanol as green solvents and its encapsulation with chitosan NPs. The developed propolis loaded chitosan NPs indicated antimicrobial and anti-biofilm properties against various gram positive and negative. FTIR revealed the successful encapsulation of the propolis extract with Ethanol (PE) and Methylal (PM) into the chitosan nano career matrix. HPLC and GC-MASS also confirmed the presence of flavonoids and phenols compounds of propolis extracted with both solvents. In addition, we confirmed the total phenolic and flavonoid compounds in propolis by calorimetric method of Folin–Ciocalteu and aluminum trichloride complex formation assays, respectively. PE-CH and PM-CH were optimized regarding physicochemical properties such as particle size, zeta potential, and poly dispersity index (PDI) index. DLS and SEM micrographs confirmed a spherical morphology in a range of 360–420 nm with Z potential values of 30–48 mV and PDI of 0.105–0.166 for PE-CH and PM-CH, respectively. The encapsulation efficiency was evaluated using colorimetric analysis, with median values ranging from 90 to 92%. The MIC values within the range of 2 to 230 µg/ml and MBC values between 3 to 346 μg/ml against both gram-positive and negative bacteria. While both PE and PM showed a significant reduction in the number of E. coli, S. aureus, and S. epidermidis, the use of PE-CH and PM-CH led to a statistically significant and greater reduction in number of E. coli, S. aureus, and S. epidermidis strains on the biofilm, pre-formed biofilm and planktonic phases. Besides, the DPPH assay showed significant antioxidant activity for these NPs within the range of 36 to 92%. MTT assay for MHFB-1, HFF, L929, MDF, and MCF-7 cells exhibited statistically significant differences in each other that show the IC50 between 60–160 µg/ml for normal cells and 20 for cancer cells. Finally the present study indicated that both PM and PM-CH greater than PE and PE-CH in which contain high flavonoid and phenolic contents with a high antioxidation potential antioxidant properties, which could be beneficial for cell proliferation and antibiotic and anticancer applications.

Microstructural characterization and corrosion behaviour of heat treated standard stainless steels in tar sand

This paper aims to investigate the corrosion behaviour of heat-treated standard duplex stainless steel (UNS S32205) in the recovery of bitumen from Nigerian-rich tar sand, using sodium hydroxide (NaOH) as the process solution. Appropriate material family needs to be identified for the exploitation of tar sand resources to ensure sustainable extraction of bitumen. UNS S32205 offers exceptional mechanical properties and excellent corrosion resistance which makes it a great material choice for demanding applications, including offshore platforms and construction projects. Samples of UNS 32205 were heat-treated and immersed in the digested tar sand, maintaining a process temperature of 90°C. The microstructure of the corrosion coupons was studied using SEM/EDS (Scanning Electron Microscope/Energy Dispersive Spectroscope), and the corrosion rate of the samples was derived using gravimetric technique following ASTM G31 standard. The SEM micrographs indicated varying degrees of pits associated with the passivity of UNS 32205 and an imbalance between its ferrite and austenite phases due to the presence of secondary precipitates formed during heat treatment.The normalized sample, having a corrosion rate of 0.053 mm/year, exhibited the best corrosion resistance, followed by oil quenching (0.054 mm/year), then annealing (0.076 mm/year), and water quenching (0.077 mm/year), where they all showed improved corrosion resistance over the as-received sample having a corrosion rate of 0.078 mm/year.

Structural, morphological, spectral properties and high quantum efficiency of Eu3+, B3+ co-activated double perovskite Ba2GdMO6 (M = Nb, Ta) phosphors

The influence of boron on the structural, morphological, and spectral properties was examined using Ba2Gd1−xMO6 (M = Nb, Ta) double perovskite ceramics co-doped with xEu3+ and yB3+ (x = 10 mol%, y = 0, 5, 15, 30, 50, 70, 100 mol%), which were synthesized through the solid-state method. X-ray diffractions of all the samples revealed a single-phase structure, and SEM micrographs of B3+, Eu3+ doped grains showed that the flux effect of boron promotes grain growth. The optical band gap energy was calculated from UV–Vis reflectance spectra, where Eg values decreased between 0 and 100 B3+. PL emissions of phosphors increase up to 50 mol% B3+ concentration due to increasing grain size and improving crystallinity, while a somewhat increase occurred in the asymmetry ratio for both series. The increase of the Judd-Ofelt (JO) parameters (Ω2 and Ω4) with increasing B3+ was associated with the decreasing local symmetry of Eu3+ sites and the decreasing electron density in the ligands. Moreover, while the increase of boron improved the quantum efficiency of phosphors, the ηQE% values of 50 mol% B3+ concentration were 80.84 % and 98.02 % for Ba2Gd1-xMO6:xEu3+, yB3+ (M = Nb, Ta), respectively. The paper may provide an alternative perspective and a new strategy for the structural, morphology, and luminescence efficiency of RE3+-doped double perovskite phosphors.

Structural and optical properties of ZnO thin films as a function of pH value and its effect on photoelectrochemical water splitting

ZnO nanoparticles were synthesised via sol–gel method, and then, deposited on a glass substrate using the spin-coating procedure to hand in ZnO thin films. In order to study the effect of alkaline sol on different properties of ZnO thin films, the pH value of sol was adjusted with ammonia. Then, the structural, optical, and photoelectrochemical properties of the prepared samples were analysed. According to XRD analyses, by increasing pH values, the size of ZnO particles increases and the films’ crystallinity improves. In addition, SEM micrographs affirm the uniformity of thin films. According to AFM findings, the morphology and roughness of the samples’ surface are affected by pH values in such a way that with increasing the pH, the roughness of the surface decreases, and the crystallinity improves. Also, both UV–vis peaks shift towards lower wavelengths with increasing pH value of ZnO sol. This means that the more the pH values of ZnO sol, the more the excitation energy of electrons. On the other hand, the numerical values of the energy bandgap decrease by increasing pH. According to PL results, the increase of pH causes the separated electrons and holes to have more energy and can move away from each other. So, the recombination process rate decreases; this result affirms by EIS findings. Increasing the optical absorption and reducing charge recombination are in favour of the photocatalytic reactions. Clearly, increasing the pH value causes the stable photocurrent to increase and the threshold voltage of (J-V) diagram to decrease. Also, the samples show recognisable sensitivity to light. As a final result, the best suggested amount of pH to fabricate ZnO photoanods for water splitting is 10.5.

Hydrophobic Coating of Vegetable-Tanned Leather with Dodecylamine

Vegetable-tanned leather exhibits a hydrophilic character due to the abundance of hydroxyl groups (-OH). In this study, the surface of vegetable-tanned leather was modified to become hydrophobic. The leather was coated using dodecylamine (DDA) through the padding method in the finishing process. The concentration of DDA varied from 1%, 2%, 3%, and 4% to identify the optimum concentration. The coating process was assisted by an activator, either acid or base, to improve the adhesion of DDA to leather. Uncoated vegetable-tanned leather was used as a control. The success of coating was identified using FT-IR and SEM-EDX analysis. The hydrophobicity of leather was conducted through a water resistance test. The success of coating is shown by the increase in their weight and thickness. Absorption bands of alkyl and amino groups of DDA are observed in FT-IR spectra around 1450 cm-1 and 3400 cm-1, respectively. SEM micrographs show that coated leathers have flatter surfaces as a consequence of DDA attachment on the leather surface. The water resistance test proves that the use of DDA can improve the leather hydrophobicity and enhance the water absorption time by up to 4 times. The optimum water absorption time is obtained when using 2% DDA.

Sustainable bioactive food packaging based on electrospun zein-polycaprolactone nanofibers integrated with aster yomena extract loaded halloysite nanotubes

Compostable zein-polycaprolactone (PZ) electrospun nanofiber integrated with different concentrations of Aster yomena extract loaded halloysite nanotubes (A. yomena-HNT) as bioactive nanofibrous food packaging is reported. SEM micrographs reveal heterogeneous nanofibers. A. yomena extract used in the study showed weak antioxidant activity with AAI and TEAC values of 0.229 and 0.346. In vitro, release profile over 7 days of A. yomena indicates a controlled, sustained, and prolonged release. The prepared nanofibers were effective against both gram-positive and gram-negative bacteria. The prepared composite nanofibers were rendered biocompatible and nontoxic when subjected to WST-1 and LDH assay after incubating with NIH 3T3 mouse fibroblast cell line. PZ-15 nanofiber packaging showed the best postharvest quality preservation in Black mulberry fruits after 4 days of storage at 25 °C and 85 % Rh. Moreover, the in vitro decomposition test reveals that the fabricated nanofibers decompose in the soil and do not pose as a threat to the environment.

Obtaining and Characterizing New Types of Materials Based on Low-Density Polyethylene and Thermoplastic Starch

Significant interest is devoted to the development of new polymer blends by using concepts of the circular economy. Such materials have predetermined properties, are easy to recycle, ecological, and have a low carbon footprint. This research presents obtaining and characterization of polymer blends based on low-density polyethylene (LDPE) and thermoplastic starch (TPS). In the first stage, TPS was obtained through the gelatinization process, and, in the second stage, mixtures of LDPE and TPS were obtained through a melt mixing process at 150 °C for 7 min. The physical–mechanical characteristics of the samples, like hardness, elongation at break, rebound resilience, and tensile strength, were determined. The sample containing maleic anhydride grafted low-density polyethylene (LDPE-g-MA) as a compatibilizer shows improvements in elongation at break and tensile strength (by 6.59% and 40.47%, respectively) compared to the test sample. The FTIR microscopy maps show that samples containing LDPE-g-MA are more homogeneous. The SEM micrographs indicate that TPS-s is homogeneously dispersed as droplets in the LDPE matrix. From the thermal analysis, it was observed that both the degree of crystallinity and the mass loss at high temperature are influenced by the composition of the samples. The melt flow index has adequate values, indicating good processability of the samples by specific methods (such as extrusion or injection).