FTIR Analysis Research Articles

Electrospun Cellulose Acetate/Poly(Vinyl Alcohol) Nanofibers Loaded with Methyl Gallate and Gallic Acid for Anti-Staphylococcus aureus Applications.

Methyl gallate (MG) and gallic acid (GA) are natural compounds with potent activity against methicillin-resistant Staphylococcus aureus (MRSA), a significant global health concern. In this study, MG and GA were incorporated into cellulose acetate (CA) blended with poly(vinyl alcohol) (PVA) to create electrospun nanofibers aimed at combating both methicillin-susceptible S. aureus (MSSA) and MRSA. Key electrospinning parameters-DC voltage, injection flow rate, and syringe tip-collector distance-were optimized, with the best conditions being a 1.5 mL/h flow rate, 30 cm distance, and 20 kV voltage. The resulting nanofiber mats were characterized by SEM, FTIR, DSC, tensile strength testing, contact angle measurement, swelling behavior, and release profiling. Antibacterial properties were assessed using the agar diffusion test. The obtained nanofibers had diameters ranging from 879.33 to 906.13 nm. Among the samples, MG-GA-CA/PVA exhibited the highest tensile strength, good flexibility, and improved stiffness, which was related to enhanced thermal stability and chemical interactions as shown by DSC and FTIR analyses. This formulation also displayed excellent hydrophilicity, swelling properties, and a consistent release profile over 8 to 24 h. Furthermore, MG-GA-CA/PVA showed superior antibacterial activity against both MSSA and MRSA, suggesting its potential as a strong, flexible, and effective anti-S. aureus material.

Crystal Evolution of Amorphous Poly(lactic acid) During Simultaneous Multi‐step Tensile Deformation and Annealing

ABSTRACTThe cold‐crystallization and crystal evolution of amorphous poly(lactic acid) (PLA) are analyzed during multistep tensile deformation and annealing at 70°C using in situ synchrotron wide‐angle X‐ray scattering (WAXS) measurements. The 2D‐WAXS diffraction pattern reveals that the PLA crystalline structure forms perpendicular to the draw direction. The annealing process lets to a rearrangement of the crystalline structure, while the stretching causes crystal contraction. Both WAXS and FTIR analyses confirm that the crystals developed through stretching and annealing are in the α′‐form. The crystallinity of PLA increases with higher deformation strains and longer annealing times. The orientation degree of both crystalline and amorphous phases of PLA, as indicated by the Hermans orientation factor and dichroic ratio of 956 cm−1 band (evaluated by WAXS and polarized FTIR analysis, respectively) also increase. The enhanced cold‐crystallization ability of PLA is attributed to the synergistic effect of tensile deformation and annealing, rather than either technique alone. The unusual crystallization phenomenon observed during multistep tensile deformation coupled with annealing provides valuable insights into the crystallization and crystal evolution of PLA.

Synthesis of new 1,4-dihydropyridine derivative, anti-cancer, bacterial activity, molecular docking and adsorption, distribution, metabolism and excretion analysis.

Aim: The amination and cyclization method developed a new strategy for designing and assembling new 1,4-dihydropyridine derivatives of compounds 3a-g and 4a-g.Methods & materials: Newly prepared pyridine compounds are more economical, and reduce the reaction time. FT-IR, 1H-NMR, 13C-NMR, mass spectroscopy and elemental analyses elucidated the synthesized derivatives. All the derivatives are subjected to in vitro assay against MCF-7 (breast) and anti-bacterial activity.Results: In the anti-bacterial activity compound 3c is moderately active against Escherichia coli (6.0g/ml), and 4c is extremely active against Lactiplantibacillus plantarum (10.0g/ml) compared with standard Erythromycin. In cytotoxic activity, the compound 3g (lC50 24.5μM) is slightly active against standard doxorubicin. We also present the outcome of a molecular docking study connecting the methoxsalen (Protein Data Bank, PDB ID: 1Z11). Compound 3g shows a higher binding affinity (-7.7Kcal/mol) matching up with doxorubicin(-9.0Kcal/mol). The synthesized analogs were predicted for their adsorption, distribution, metabolism and excretion profiles and pharmacokinetics. The compound 3g has three rotatable bonds (NROB≤10), five hydrogen bond acceptors (HBA≤10) and four hydrogen bond donors (HBD≤5). All the compounds follow Lipinski's rule.Conclusion: Therefore, the compounds 3c and 3g are used as cytotoxic and anti-bacterial drugs in feature.

Sustainable Management of Agro-Food Wastes Derived from the Olive Mill and Sugar Industry and Clinoptilolite to Produce Novel Adsorptive Materials

Novel sorbents were produced using sustainable and eco-friendly methods, aimed at minimizing environmental impact while utilizing industrial by-products and natural minerals. Olive stones and molasses derived from olive mill and sugar industries, respectively, and an abundant, natural and low-cost mineral, clinoptilolite, were combined in the following proportions: 80/20 clinoptilolite/stone, 80/10/10 clinoptilolite/stone/molasses, 50/50 stone/molasses, w/w. Then, physical carbonization (CL80OL20C, CL80OL10M10C, OL50M50C) or chemical activation (CL80OL20A, CL80OL10M10A, OL50M50A) took place. The adsorbents were characterized through Raman, FT-IR, BET and SEM-EDS analysis. The CL80OL20A material presents the highest ratio of C/O in EDS analysis and the lowest ID/IG in Raman spectroscopy. The increase in the specific surface area is as follows: OL50M50C < OL50M50A < CL80OL10M10C < CL80OL20C < CL80OL20A < CL80OL10M10A. Three applications were conducted: two with dyes (methylene blue and methyl red) in aqueous means and one in olive mill wastewaters for the removal of total phenols and their addition to rice, increasing the total phenolic content and producing novel foods. The well-fitted application of the pseudo-second order kinetic model to the experimental data has shown that chemisorption is the prevailing mechanism. The adsorbed amount of the recovered phenols to rice ranges from 0.14 to 0.93 mg/g. Consequently, olive and sugar by-products can be used as filters either to adsorb dangerous organic compounds or to recover bioactive compounds from wastewater, preventing their disposal in the environment, which could otherwise lead to severe negative effects on the ecosystems.

Study on interfacial tension, wettability and viscosity in different salinities of synthesized a new polymeric surfactant for improving oil recovery

Over 50% of the original oil in place (OOIP) is immobile or trapped in the reservoir. Therefore, today, more efficient methods have been introduced in the tertiary oil recovery sector as a scheme of enhanced oil recovery (EOR). Due to the decline of conventional hydrocarbon reserves, polymers are increasingly used in EOR methods, such as surfactant-polymer (SP) and alkaline-surfactant-polymer (ASP) flooding. SP flooding has a complex formulation and design, leading to undesirable phase separation if improperly mixed. Polymeric surfactants are a promising alternative to SP flooding. They consist of hydrophobic groups attached to hydrophilic polymers, which help to improve the mobility ratio and reduce interfacial tension (IFT). This paper examines the rheological and synthesis properties of a new polymeric surfactant produced through bond co-polymerization reaction using different hydrolyzed polyacrylamide (HPAM) ratios and a zwitterion hydrophobic group. The synthesized hydrophobically modified zwitterionic polyacrylamide (HMZPAM) was characterized by FTIR and HMNR analysis. HMZPAM performed better than other substances in IFT, viscosity, wettability, oil recovery, and resistance to different one and two-valence cations. The results indicate that HPAM reduced the IFT to 13.65, while HMZPAM reduced it to 0.441 mN/m. Wettability change evaluated on a rock carbonate/crude oil/HMZPAM system that changed the water-wet state of the primary oil-wet rock carbonate to strongly water-wet state as wettability change measurements showed a decrease in contact angle from 62.76 to 21.23 degree. Comparative studies on the effectiveness of HPAM and HMZPAM were also conducted according to the measurement of viscosity and shear rate in the presence of salt, which indicates the higher shear rate and viscosity of HMZPAM. Core flooding tests revealed that HMZPAM resulted in better additional recovery due to microscopic displacement, resulting in a total oil recovery of 84%, compared to 48% of residual oil saturation for HPAM. Also, salts decreased oil recovery in HPAM injection but increased oil recovery in HMZPAM injection.

Nano Hydroxyapatite (Nano-HA) Based on Pholas Orientalis Shells and Degradation Analysis

Millions of tons of seashells are produced every day as waste around the world. These underutilized seashells waste was executed as calcium precursor by researcher to synthesis the nano-hydroxyapatite (nano-HA). Nano-HA was successfully synthesised from Pholas Orientalis seashells waste via the chemical precipitation method. Different sintering temperatures were implemented to evaluate the physicochemical criteria of nano-HA. The obtained powders were examined by various physicochemical methods such as XRD, FTIR, FESEM, EDX and degradation analysis. The peaks in XRD and FTIR analysis the HA is successfully produced. The FESEM images on the other hand showing the HA particle in nano size range with rice-like structure. Meanwhile, a variation of Ca/P ratio can be observed in respect to sintering temperatures. The Ca/P ratio for HA-WS, HA-S500 and HA-S700 sample is 1.78, 2.03 and 1.57 respectively. Different sintering temperatures result in different crystallinity value which consequently affects its degradation profile.

An environmental approach to cement admixtures: Utilization of waste olive seed powder as a bio-polymeric admixture.

The integration of organic wastes into cement-based materials shows promise as a solution to mitigate environmental pollutants. It achieves this by minimizing waste sent to landfills and in some conditions decreasing Portland cement use. One of these organic wastes that produces positive effects when used in cement products is olive seed. In this study, the effect of a new generation bio-polymeric admixture on the physical and mechanical properties of cement mortars is examined in detail. The bio-polymeric admixture is prepared by grinding olive seeds in 0/125μm sizes. The olive seeds have been used as bio-polymeric admixture in cement mortars at different rates, i.e., 0, 0.2, 0.35, 0.5, 1 and 1.5% of total weight. The olive seed is characterized by XRD, FT-IR analysis and by determining extracts, pectin, cellulose, hemicellulose and lignin content. The characteristics of hydration products were analyzed by SEM/EDS and XRD investigations. Effect of bio-polymeric admixture addition on the unit weight, flowability, setting time, compressive and flexural strength and capillary water absorption was analyzed. The results suggested that the bio-polymeric admixture hindered the cement hydration at low usage rates but promoted at high usage rates. Accordingly, 28days compressive and flexural strength of test samples decreased. However, 1.5 wt% bio-polymeric admixture was associated with a slight increase of 150-days compressive strength. Bio-polymeric admixture improves the hydrophobicity property of the hardened mortar samples by declining effect on the water absorption. Another important effect of the bio-polymeric admixture contribution was also observed on the flowability property of the cement mortars. As the bio-polymeric admixture increased, the flow diameter values of the mortar were also significantly increased. The research outcomes suggested for the first time the beneficial effect of bio-polymeric admixture as a natural and bio-degradable alternative of chemical admixtures on especially flowability, set retarder and hydrophobicity of cement mortars with comparable mechanical properties.

Fabrication of drug loaded polylactic acid/keratin/polyethylene glycol GTR membrane for periodontal application

This study proposes the fabrication of, amoxicillin-loaded composite GTR membranes from polylactic acid (PLA), wool keratin (WK), and polyethylene glycol (PEG) for periodontal therapy. Deep eutectic solvents were employed for the extraction of keratin from wool fibers. For the preparation of the control (C), PLA and PEG were dissolved in a ratio of 60:40 in chloroform. While the experimental groups K2 and K3 were prepared by adding, 2% and 3% WK powder, respectively, to the control mixture. To prepare the experimental groups K2-D and K3-D, 1% AMOX-treated WK powder was mixed with the previously mentioned groups. The prepared GTR membrane was characterized using various analytical techniques. The treatment of sheep wool and the presence of AMOX in the experimental groups were confirmed using FTIR analysis. The Scanning electron microscope (SEM) images of the prepared GTR membranes showed voids and presented a conglomerated appearance. The K2 had the highest tensile strength, whereas K2-D and K3-D which contained drugs had lower tensile strengths but significant antibacterial activity. K2 experienced the greatest mass change after 1 h, while K2-D and K3-D experienced the least. Each membrane was found to be hydrophilic. The Alamar Blue Assay revealed good biocompatibility.

The Stability Challenge of Furanic Platform Chemicals in Acidic and Basic Conditions.

The transition toward renewable resources is pivotal for the sustainability of the chemical industry, making the exploration of biobased furanic platform chemicals derived from plant biomass of paramount importance. These compounds, promising alternatives to petroleum-derived aromatics, face challenges in terms of stability under synthetic conditions, limiting their practical application in the fuel, chemical, and pharmaceutical sectors. Our study presents a comprehensive evaluation of the stability of furan derivatives in various solvents and under different conditions, addressing the significant challenge of their instability. Through systematic experiments involving GC‒MS, NMR, FT‒IR and SEM analyses, we identified key degradation pathways and conditions that either promote stability or lead to undesirable degradation products. These findings demonstrate the strong stabilizing effect of polar aprotic solvents, especially DMF, and reveal the dependence of furan stability on solvent and additive type. This research opens new avenues in the utilization of renewable furans by providing critical insights into their behavior under synthetic conditions, significantly impacting the development of sustainable materials and processes. The broad appeal of this study lies in its potential to guide the selection of conditions for the efficient and sustainable synthesis of furan-based chemicals, marking a significant advance in green chemistry and materials science.

Recovery of precious metals from aqua regia leachate of e-wastes using dithiocarbamate-modified cellulose and development of a novel kinetic model

The escalating demand and dwindling natural supplies of precious metals (PMs) necessitate innovative hydrometallurgical recovery approaches with rapid kinetics and reduced environmental impact. The current study investigated the sorption and recovery of PMs from electronic waste (e-waste) utilizing dithiocarbamate-modified cellulose (DMC) and its proline derivative with epoxy cross-linkage (DMC-Pro-Epo-6) in aqua regia (AR). The effects of various sorption parameters, such as sorbent dose in feed, HCl:HNO3 ratio, AR dilution times, etc., on PM recovery were explored. Equilibrium for AuIII and PtIV sorption by DMC and DMC-Pro-Epo6 was reached in less than an hour, which is significantly faster than most reported sorbents. The maximum sorption capacities in AR settings, calculated using the Langmuir equation, were 348.0 mg g−1 for AuIII and 34.7 mg g−1 for PtIV for DMC, while DMC-Pro-Epo6 achieved 350.3 mg g−1 for AuIII and 31.1 mg g−1 for PtIV. These capacities, particularly for the higher sorption capacity of AuIII by DMCs, are attributed to the relativistic effects of gold, soft–soft interactions, and strong sulfur binding. FT-IR, FE-SEM, and EDX analyses elucidated the chelation bonding and mechanisms involved in PM sorption onto DMCs. By utilizing AR-DMC integrated techniques, step-by-step protocols were established for Au recovery from diverse e-waste sources, such as smartphones and smart chip cards. The study also highlighted the importance of chemical pre-concentration of e-waste to remove base metals, facilitating efficient PM recovery. Finally, a key innovation of this work is introducing a new pseudo-mix order fractional model, based on the preference of active sites with fractional assumptions, which more accurately correlates the sorption kinetics observed in complex systems.

Physicochemical and biological evaluation of ‘click’ synthesized vinyl epoxide-chitosan film for active food packaging

Chitosan (Cs) being a natural biopolymer serves as an excellent template to construct active packaging materials for achieving sustainable development. In this study, Cs was chemically modified via epoxide ring opening click reaction using vinyl epoxide to obtain a novel chitosan vinyl epoxide (Cs-VE) derivative with hydroxyl and olefinic functional groups. The Cs-VE transparent film was fabricated through the eco-friendly solution casting technique. A meticulous investigation into the chemical structure and physicochemical properties of the synthesized films was conducted using FT-IR, 1H NMR and XRD analyses. The thermal stability and homogeneity of the film were verified by thermogram and FE-SEM images respectively. Improved mechanical properties (tensile strength of 24.64 MPa and 12.08 % elongation at break) and excellent UV-light blocking ability (9.3 % transmittance at 350 nm and 22.15 % transparency at 600 nm) were observed. Also, important parameters such as water vapor permeability (WVP), swelling degree, water solubility and UV-barrier properties were found to be adequate for food packaging application. Similarly, enhanced antioxidant activity with 27.2 % and 73.6 % radical scavenging against DPPH and ABTS radicals respectively was observed for the synthesized Cs-VE film. The film showed antimicrobial activity against both bacteria and fungi. These results along with food packaging studies on Grewia asiatica fruit established the developed Cs-VE film as a suitable candidate for active food packaging application.

Corrective role of endophytic exopolysaccharides from Clerodendrum infortunatum L. on arsenic-induced ovarian steroidogenic dysfunction and associated inflammatory responses

The present investigation aimed to evaluate the therapeutic potential of exopolysaccharides (EPSs) derived from endophytic fungi against arsenic [As(III)]-mediated metabolic and reproductive ailments. Two endophytic fungi, Diaporthe arengae (CleR1) and Fusarium proliferatum (CleR3), were isolated from Clerodendrum infortunatum (Cle), and used for the extraction of two types of EPSs. GC–MS analysis confirmed the presence of hydroxymethyl furfural (HMF) and α-d-glucopyranose in the EPS1 (CleR1) and EPS2 (CleR3), respectively. FTIR analysis revealed the potential As(III)-chelation properties of both EPSs. EPS1 and EPS2 significantly mitigated As(III)-induced oxidative stress and lipid peroxidation by restoring the activities of antioxidative enzymes. EPSs successfully corrected the gonadotropin imbalance and steroidogenic alterations. The downregulation of proinflammatory (NF-κB and TNF-α) and proapoptotic (BAX) mediators and the upregulation of antiapoptotic (Bcl-2) markers were also detected following the treatment with EPSs. Histomorphological restoration of reproductive and metabolic organs was also observed in both the EPS groups. Moreover, the As(III)-induced increase in the immunoreactivity of the androgen receptor (AR) was successfully reversed by these EPSs. Molecular docking predicted that HMF and α-d-glucopyranose of EPS1 and EPS2 interact with the active site of AR by limiting its activity. Hence, EPS could be effective for developing new therapeutic strategies for managing As(III) toxicity.

The Effect of Carbodiimide Crosslinkers on Gelatin Hydrogel as a Potential Biomaterial for Gingival Tissue Regeneration

Connective tissue grafts for gingival recession treatment present significant challenges as they require an additional surgical site, leading to increased morbidity, extended operative times, and a more painful postoperative recovery for patients. Gelatin contains the arginine–glycine–aspartic acid (RGD) sequence, which supports cell adhesion and interactions. The development of gelatin hydrogels holds significant promise due to their biocompatibility, ease of customization, and structural resemblance to the extracellular matrix, making them a potential candidate for gingival regeneration. This study aimed to assess the physical and biological properties of crosslinked gelatin hydrogels using EDC/NHS with two crosslinker concentrations (GelCL12 and GelCL24) and compare these to non-crosslinked gelatin. Both groups underwent morphological, rheological, and chemical analysis. Biological assessments were conducted to evaluate human gingival fibroblast (HGF) proliferation, migration, and COL1 expression in response to the scaffolds. The crosslinked gelatin group exhibited greater interconnectivity and better physical characteristics without displaying cytotoxic effects on the cells. FTIR analysis revealed no significant chemical differences between the groups. Notably, the GelCL12 group significantly enhanced HGF migration and upregulated COL1 expression. Overall, GelCL12 met the required physical characteristics and biocompatibility, making it a promising scaffold for future gingival tissue regeneration applications.

“Chacco” clay from the Peruvian highlands as a potential adsorbent of heavy metals in water

This research aimed to remove Cd (II), Cr (VI), Ni (II), Pb (II), and V (V) from aqueous solutions prepared in distilled water using “Chacco” clay from the Peruvian highlands as adsorbent. The adsorption process was carried out in Batch type systems for 120 min using solutions of each metal at a concentration of 5 mg/L in aqueous systems of a single metal or monometallic (MAS) and solutions of the five metals simultaneously or multimetallic (MMAS). For this purpose, the “Chacco” clay was first characterized by SEM-EDS analysis, finding a laminated clay structure with an elemental composition of C, Al, Fe, Na, Mg, Ca, K, As, Cu, Pd, O, and Ta. The results using 10 g/L of “Chacco” clay showed that the best adsorption efficiency in both MAS and MMAS aqueous systems is achieved at pH = 4 achieving in MAS aqueous systems the removal of 64.16 ± 0.98 % of Cd (II), 95.70 ± 0.81 % of Cr (VI), 97.20 ± 0.89 % of Ni (II), 92. 78 ± 0.79 % of Pb (II), and 95.80 ± 0.67 % of V (V), on the other hand, in aqueous MMAS systems a decrease in adsorption efficiency was observed, managing to remove 6.88 ± 0.53 % of Cd (II), 63.04 ± 0.94 of Cr (VI), 7.81 ± 0.43 % of Ni (II), 62.34 ± 0.77 % Pb (II), and 14.33 ± 0.56 % of V (V). The kinetic study showed that the adsorption mechanism would correspond to chemisorption since the process fitted best to the pseudo-second order model and Elovich. SEM-EDS analysis after adsorption confirmed the presence of the heavy metals under study in the “Chacco” clay. Metal adsorption is evidenced at 1418 cm−1 by -CH2-metal deformation vibrations according to FTIR analysis. In conclusion, the “Chacco” clay would be a promising adsorbent of heavy metals in polluted waters so that scaling up to real environments could be feasible. On the other hand, the “Chacco” clay is consumed by the population of Puno, Peru, therefore its potential impact on health should be evaluated due to its capacity to accumulate metals and the presence of Al in this clay.

Green synthesis of anethole-loaded zinc oxide nanoparticles enhances antibacterial strategies against pathogenic bacteria.

The threat of antibiotic resistance is escalating, diminishing the effectiveness of numerous antibiotics due to the rapid development of resistant bacteria. In response, the use of green-synthesized nanoparticle, alone or combined with antimicrobial agents, appears promising. This study explores the effectiveness of zinc oxide nanoparticles (ZnONPs) synthesized using Loranthus cordifolius leaf extracts and subsequently coated with anethole. The fabrication of these nanoparticles was confirmed via UV-Vis, FTIR and TEM analyses, ensuring the nanoparticles were produced as intended. Utilizing a nanoprecipitation process that excludes evaporation and drying, a high drug loading capacity of 16.59% was accomplished. The encapsulation efficiency for anethole was recorded at 88.23 ± 4.98%. Antibacterial efficacy was assessed by com paring the green-synthesized ZnONPs (average size: 14.47nm), anethole-loaded ZnONPs (average size: 14,75nm), and commercially sourced ZnONPs. The ZnONPs with anethole demonstrated superior inhibition against all tested bacterial strains, including Gram-negative species like Pseudomonas aeruginosa and Escherichia coli, and Gram-positive species like Bacillus subtilis and Staphylococcus aureus, outperforming the commercially available ZnONPs. Additionally, anethole-coated ZnONPs showed the greatest inhibition of Gyr-B activity (IC50 = 0.78 ± 0.2M), better than both green-synthesized and commercially available ZnONPs. These findings emphasize the enhanced antimicrobial properties of ZnONPs, particularly when combined with green synthesis and anethole loading, highlighting their potential in various biomedical applications.

Efficient conversion of xylose and corncob to furfural using a novel carbon-based solid acid derived from black liquor lignin-tin complexes

The novel carbon-based solid acid catalyst was prepared by carbonizing the mixture of metal salts and black liquor, followed by sulfonating. The physicochemical properties of the catalysts were characterized by SEM, FTIR, BET, NH3-TPD, Py-IR, XPS, ICP, and elemental analysis. The catalytic ability of the catalyst was explored by converting xylose and corncob to furfural via a one-step process. The effects of solvent types and water contents, catalyst dosage, substrate concentration, reaction temperature, and reaction time on furfural yield were evaluated. 93.4 % of furfural yield was achieved using 200 mg xylose at 170 °C for 120 min with 150 mg catalysts. Moreover, the furfural yields of 82.5 % were obtained from corncob. This work provides a promising strategy for synthesizing carbon-based solid acid catalysts from pulp waste black-liquid resources, which has a potential application for producing furfural from hemicellulose.

Characterization of the natural fibers extracted from the aninga's stem and development of a unidirectional polymeric sheet.

A unidirectional sheet was made with oriented fibers in an epoxy matrix. Natural fibers were extracted from the stem of Montrichardia linifera (Arruda) Schott., traditionally known as aninga, characterized and used to produce a unidirectional polymeric sheet. FTIR, XRD, SEM, TG, and DTG analyses were performed to characterize these cellulose fibers. Peaks observed at 1024cm- 1, 1600cm- 1, and 3328cm- 1 revealed the stretching vibration of the O-H bond, the stretching of the carbonyl in hemicellulose, and the vibration of aromatic rings, respectively. XRD analysis demonstrated a crystallinity index of 62.21%. Morphological analysis revealed the microstructural quality of the fiber surface, with grooves for mechanical anchoring, as well as its interior, which is composed of microfibrils. EDS analysis confirmed the presence of the main elements composing natural fibers, with carbon being the major component (70%). The thermal stability of aninga fibers was up to 450 ºC for the degradation of 50% of their initial mass. The mechanical properties of untreated aninga fibers showed a tensile strength of 332MPa and an elastic modulus of 13.000MPa. The unidirectional sheet had a tensile strength of 4.5MPa and an elasticity modulus of 332.9MPa. These outcomes ensured that aninga fiber is considered high-performance (> 200MPa) and can be used for internal automobile components.

Eco-friendly Synthesis of Gold Nanoparticles of Methanolic Extract of Bauhinia vahlii Leaves and Evaluation of Tyrosinase Inhibitory Activity

Background: The green synthesis of gold nanoparticles (AuNPs) using natural materials has gained significant attention in recent years due to their eco-friendliness and potential applications in various fields. Methods: The present study aimed at the green synthesis and anti-hyperpigmentation potential of gold nanoparticles (AuNPs) using a methanolic extract of Bauhinia vahlii. Furthermore, the green synthesis of the AuNPs was confirmed by UV-visible, FT-IR, XRD, and EMDEX analysis. The size and surface topological significance of green synthesized AuNPs were evaluated through Scanning Electron Microscope and Field Emission Scanning Electron Microscopy. Results: The size of the synthesized AuNPs was found to be in the range of 100-1000 nm. The tyrosinase inhibitory activity of AuNPs was evaluated through the mushroom tyrosinase inhibitory assay method. The tyrosinase inhibitory activities of crude extract, AuNPs, and Kojic acid were found to be 98.7 ±0.7, 75±1.3 and 41±1.1 μg/ml, respectively. Conclusion: Hence, green synthesized AuNPs of B. vahlii leaf extract may be used as a potent antihyperpigmentation agent in the market of nano cosmeceuticals.

Effect of Polyethylene Glycol Concentration on the Structural and Mechanical Properties of Polysulfone-Based Membranes

Water pollution in Indonesia is a growing concern, necessitating the development of advanced treatment technologies. Membrane-based filtration, a promising approach due to its low energy consumption and ability to preserve material properties, has been explored. Polysulfone (PSf), a commonly used membrane material, is known for its thermal stability, chemical resistance, and mechanical strength. However, its hydrophobic nature limits its filtration performance. To enhance hydrophilicity and porosity, polyethylene glycol (PEG) is introduced as a hydrophilic additive. This study investigated the synthesis of PSf/PEG composite membranes with varying PEG concentrations (0%, 9%, and 14%) using the phase inversion method. Characterization of the membranes revealed that increasing PEG content led to thinner membranes with higher porosity, density, and swelling capacity. While Membrane-A (100% PSf) exhibited the highest tensile strength, Membrane-B (9% PEG) demonstrated the greatest elongation. SEM analysis confirmed that higher PEG concentrations resulted in larger and more numerous pores, forming asymmetric structures suitable for filtration. FTIR analysis verified the successful integration of PEG into the PSf matrix. The findings highlight the potential of PEG-modified PSf membranes for industrial wastewater treatment. The M-C membrane, containing 14% PEG, exhibited the highest swelling degree, indicating improved hydrophilicity and permeability. However, increased PEG content also led to decreased tensile strength. The optimized M-C membrane, with a density of 0.9906 g/cm³, a mass of 1.9249 g, and a thickness of 102 µm, meets the requirements for effective water treatment applications. This research contributes to the development of sustainable membrane technologies for environmental management in Indonesia. By addressing the limitations of PSf membranes, PSf/PEG composite membranes offer a promising solution to water pollution challenges in the region.

Effect of Shikimic Acid on Oxidation of Myofibrillar Protein of Duck Meat During Heat Treatment.

The myofibrillar protein (MP) of duck meat is prone to excessive oxidation during thermal processing, resulting in a decline in its overall quality. In this paper, the effect of shikimic acid on the oxidative structure of duck muscle fibrin was studied. The findings showed that, at a mass ratio of 1:50,000 (g/g) between shikimic acid and MP, the carbonyl content of MP was reduced by 74.20%, while the sulfhydryl content was increased by 73.56%. MP demonstrated the highest denaturation temperature, whereas its thermal absorption was the lowest. The percentage of α-helixes and β-sheets increased by 16.72% and 24.74%, respectively, while the percentage of irregular structures decreased by 56.23%. In addition, the surface hydrophobicity index of MP exhibited a significant decrease (p < 0.05), while there was a significant increase in its free radical-scavenging ability (p < 0.05). Molecular fluorescence spectrum analysis showed that shikimic acid could bind to MP, altering the internal environment of MP and enhancing its thermal stability. FTIR analysis showed that shikimic acid could enhance the distribution of protein particle sizes by reducing irregular structures, the proportion of β-rotation, and the degree of protein aggregation. It is hoped that this research can offer scientific support for improving meat processing technology.