Fourier Transform Infrared Spectroscopy Data Research Articles

Мultivariate analysis for rapid screening and prediction of solid-state compatibility in pharmaceutical preformulation studies-paving the road for machine learning

Multivariate analysis models were developed to evaluate the results obtained from a compatibility study designed for ibuprofen with a large group of different types of excipients, as a possible approach for rapid screening of the incompatibility between the active pharmaceutical ingredient (API) and excipients. The solid-state characterization of the binary mixtures was performed by Fourier transform infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC). Principal component analysis (PCA) and partial least squares-discriminant analysis (PLS-DA) using SIMCA® software were applied for evaluation of the experimentally obtained results. The optimal PCA model for the FTIR spectra explains 96.2 % of the variations in the dataset with good statistical indicators (R2X = 0.960, Q2 = 0.900), which was also the case for the PCA model for the DSC curves (R2X = 0.981, Q2 = 0.866). The applied PLS-DA models have shown similar behaviour to the PCA. Moreover, the main spectral variations in the FTIR spectra and the thermal events in the DSC data were attributed the highest variable importance for the projection (VIP) scores in the corresponding VIP plots, confirming the model capability for predicting ibuprofen interactions. Furthermore, the prediction power of the optimal models for FTIR and DSC experimental data was evaluated by the root mean square error of prediction (RMSEP) of 0.10 and 0.16, respectively. The obtained results demonstrated the potential of multivariate statistical analysis as a machine learning-based technique for screening and prediction of ibuprofen-excipients solid-state compatibility in the preformulation phase of the pharmaceutical development of dosage forms.

Improved photocatalytic activity of (Ni, Mn) co-doped ZnO nanoparticles prepared via green synthesis route using orange peel extract

(Ni–Mn) co-doped ZnO nanoparticles were synthesized for different doping concentrations (1 %, 2 %, and 3 %) and compared with the purely synthesized ZnO nanoparticles. Green synthesis route was followed to fabricate both pure and co-doped ZnO nanoparticles and the orange peel extract was used as the reducing agent. The main objectives of this research were to reduce the use of toxic chemicals and develop an eco-friendly green route for both pure and doped ZnO nanoparticle synthesis. Additionally, the co-doping effect on the photocatalytic activity was also observed. The synthesized particles were extensively characterized by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM) analysis, Fourier Transform Infrared spectroscopy (FTIR), and Ultraviolet–visible (UV–vis) spectroscopy. XRD analysis confirmed the exitance of ZnO nanoparticles with wurtzite structure. No extra peaks were found for the co-doped sample confirming the successful doping. The crystallite size decreased after doping and the range varied from 36 nm to 35 nm with increasing doping concentration. SEM analysis revealed the average particle size ranging from 66.42 nm to 37.52 nm with increasing doping concentration, the particle was irregular in shape, and agglomeration was observed. The FTIR data unveiled the existence of Ni–O, Mn–O, and Zn–O bands in the synthesized materials. The band gap of the NPs was determined from the UV–Visible spectroscopy analysis which varied from 3.30 eV to 2.71 eV with increasing doping concentration. The photocatalytic activity significantly improved with the increment of the doping concentration. The 2 % and 3 % doped samples degraded almost 97 % of the methylene blue dye at 30 min.

Influence of Biogenic Material Content on the Biodegradability of Styrene-Butadiene Composites with Incorporated Chlorella vulgaris Biomass.

Bio-fillers are intensively studied for advanced polymer composite circular design and production. In this context, the algal biomass may be considered an important and relatively low-cost resource, when harvested as a by-product from wastewater treatment plants. The biomass of the algal species Chlorella vulgaris is frequently used in this type of environmental process, and its macro constituents' composition ranges from around 15-25% carbohydrates, 10-20% lipids, and 50-60% proteins. Poly (styrene-butadiene-styrene) (SBS) copolymers have a matrix composed of glassy polystyrene domains connected by flexible polybutadiene segments. Although the physical-mechanical properties of SBS copolymers recommend them for many industrial applications, they have the drawback of low biodegradability. This study aimed to assess the aerobic biodegradability of polymer composites by integrating biomass from Chlorella vulgaris at varying mass percentages of 5, 10, and 20% into SBS copolymer composites. Biodegradation tests were conducted under industrial composting conditions (58 °C and 50% relative humidity) for 180 days. The biodegradability of materials was evaluated by measuring the CO2 produced in each vessel during the study period. Potential correlations between the amount of carbon dioxide released and the percentage of biomass added to the polymer matrix were examined. Structural and morphological changes were assessed using Fourier Transform infrared spectroscopy (FTIR), thermal analysis (DSC), and scanning electron microscopy (SEM). Physical and chemical testing revealed a decrease in sample density after the industrial composting test, along with noticeable changes in melt flow index (MFI). The observed physical and chemical changes, coupled with FTIR, SEM, and DSC data, indicate increased cross-linking and higher porosity in biodegraded polymer structures with higher biomass content. This behavior is likely due to the formation of cross-linked connections between polymer chains and polypeptide chains resulting from protein degradation, enhancing connections between polystyrene units facilitated by peptide bonds with the benzene units of the styrene blocks within the polymer matrix.

Binary Mixtures of Meloxicam and L-Tartaric Acid for Oral Bioavailability Modulation of Pharmaceutical Dosage Forms.

Binary mixtures of active pharmaceutical ingredients (API) are researched to improve the oral bioavailability of pharmaceutical dosage forms. The purpose of this study was to obtain mixtures of meloxicam and L-tartaric acid because tartaric acid improves intestinal absorption and meloxicam is more soluble in a weakly basic environment. The mixtures in the 0-1 molar fraction range, obtained from solvent-assisted mechanosynthesis, were investigated by differential scanning calorimetry (DSC), Fourier Transform Infrared (FTIR) spectroscopy, Fourier Transform Raman spectroscopy (FT-Raman), X-ray powder diffraction (XRD) and solubility tests. The physicochemical characteristics of the compounds obtained from DSC data reveal, for the first time, the formation of a co-crystal at meloxicam molar fraction of 0.5. FTIR spectroscopy data show the existence of hydrogen bonds between the co-crystal components meloxicam and L-tartaric acid. FT-Raman spectroscopy was used complementary with FT-IR spectroscopy to analyze the pure APIs and their mixtures, to emphasize the appearance/disappearance and the shifts of the position/intensity of vibrational bands, following the formation of hydrogen-bonded structures or van der Waals interactions, and to especially monitor the crystal lattice vibrations below 400 cm-1. The experimental results obtained by X-ray powder diffraction confirmed the formation of the co-crystal by the loss and, respectively, the apparition of peaks from the single components in the co-crystal diffractogram. The solubility tests showed that the co-crystal product has a lower aqueous solubility due to the acidic character of the other component, tartaric acid. However, when the solubility tests were performed in buffer solution of pH 7.4, the solubility of meloxicam from the co-crystal mixture was increased by 57% compared to that of pure meloxicam. In conclusion, the studied API mixtures may be considered potential biomaterials for improved drug release molecular solids.

Investigation of the affinity and interaction of fibrinogen with trehalose as a protein stabilizer

Trehalose, a remarkable substance, holds great importance in biomedicine for its anti-inflammatory properties and its capacity to hinder scar formation at wounds. This study aims to explore how trehalose interacts with fibrinogen, a crucial protein in wound healing, paying particular attention to their structural characteristics. An array of analytical methods, such as steady-state fluorescence, UV–Vis analysis, circular dichroism (CD), Zeta potential measurements, Dynamic light scattering (DLS), and Fourier-transform infrared spectroscopy (FT-IR), are employed to examine the influence of trehalose on fibrinogen. The findings demonstrate that trehalose induces structural alterations on the surface of fibrinogen, resulting in its compaction. Moreover, computational modeling approaches like docking and molecular dynamics simulations are utilized to enhance the understanding of the interactions between trehalose and fibrinogen. The findings indicate the establishment of a stable complex between the two entities, accompanied by slight modifications in the protein's structure due to their interaction. The main forces facilitating the bonding of trehalose (the ligand) and the protein are hydrogen bonds and van der Waals forces, resulting in an entropy-driven spontaneous bonding process. FT-IR data reveals the emergence of fresh bonds between fibrinogen and trehalose post their interaction, whereas Zeta potential investigations suggest that the engagement with trehalose enhances the stability of the protein structure.Tests assessing cytotoxicity on a typical fibroblast cell line demonstrated that the fibrinogen-trehalose compound displays lower toxicity levels compared to trehalose alone. This suggests a milder impact on cells from the compound. Moreover, molecular docking analysis supports these experimental results, indicating that trehalose molecules primarily bind to the C-terminal end of the coiled-coil segment and the globular area of the Bβ chain within the Dβ fragment. These outcomes highlight the promise of trehalose as a valuable material for wound dressing purposes.

Quantifying Ageing of 35-50 and 70-100 Asphalts Using Fourier Transform Infrared Spectroscopy and Dynamic Shear Rheometer Measurements

In this study, Dynamic Shear Rheometer (DSR) and Fourier Transform Infrared (FTIR) spectroscopy tests were performed on 35-50 and 70-100 penetration-graded asphalts. Both tests were performed on specimens at three different ageing states: unaged, short-term aged using the standard rolling thin film oven (RTFO) device, and long term aged by placing RTFO residue in the pressure aging vessel (PAV) apparatus. The tests were accomplished to quantify how ageing affects the results of both tests, namely the complex shear modulus for the DSR test and the carbonyl, sulfoxide, and ageing indices for the FTIR spectroscopy test. Both sets of measurements confirm that the harder asphalt stays harder than the softer asphalt after undergoing ageing, but the rate of hardness is higher for the softer asphalt. For instance, on average, PAV ageing was found to increase the amplitude of the shear complex modulus, from the unaged state, by 4.3 times and by 6.2 times for the 35-50 and 70-100 asphalts, respectively. It was also found that ageing decreases the phase angle for asphalt and the decrease is more pronounced for the softer asphalt (70-100) than the harder one (35-50). This was attributed to more maltenes content in the softer asphalt that transform into asphaltenes during ageing. Correlation coefficient between FTIR signals from the same samples revealed that FTIR spectroscopy as used in this research has an excellent repeatability. The repeatability was also confirmed using measures of dispersion such as the coefficient of variation, which was found not to exceed the 1.2%. The 35-50 asphalt was found to have more C=O and S=O links than the 70-100 asphalt since it showed more absorbance in the carbonyl and sulfoxide bands. These links are thought to make the asphalt physically harder. An analysis of variance study revealed that ageing is a statistically significant factor as measured using ageing indices calculated from FTIR spectroscopy data with the index AIFTIR being the most sensitive to ageing among all considered indices. Empirical power equations with high coefficient of determination values were established to predict DSR results from FTIR index values, which was possible since both types of measurements show the same trend with ageing.

Pore scale investigation of chelating agents flooding for enhanced oil recovery

Recently, laboratory tests have shown a positive response to chelating agent brines in sandstone and carbonate reservoirs as a new enhanced oil recovery technique. There is little research on direct and visual evidence of underlying mechanisms behind the chelating agent effects. In this study, a microfluidic method was established using glass micromodel to investigate the micro-mechanisms of displacement under ethylenediaminetetraacetic acid (EDTA) and diethylenetriaminepentaacetic acid (DTPA) chelating agent at the pore-scale level. Furthermore, for the study of fluid/fluid interactions, EDTA brine and DTPA brine were brought into contact with two different crude oils to examine the possible compositional changes. For this purpose, sample tests, Fourier Transform Infrared Spectroscopy (FTIR), microscopic image analysis, and dynamic interfacial tension (IFT) measurements were conducted. The FTIR data showed EDTA brine and DTPA brine induced changes in the oil sample composition compared to seawater, which can be related to the formation of water-in-oil micro-dispersions. Microscopic image analysis on samples confirmed the formation of these micro-dispersions. The visual study by the micromodel demonstrated the micro-dispersion formation in the tertiary injection of EDTA and DTPA brine. Based on the observation made, the pore-scale mechanisms of chelating agent flooding involve the chelating agent brine penetrating the crude oil, resulting in micro-dispersion formation. These micro-dispersions tend to alter wettability to a more water-wet state, facilitate oil detachment from the surface, redistribution of oil saturation, and thus leading to improved oil recovery. The observed IFT reduction aids the penetration of EDTA and DTPA brine into the crude oil to form micro-dispersions.

Synthesis and Characterization of Ni/Al Layered Double Hydroxides Composite Based-Material with Chitosan, Cellulose, and Graphene Oxide

In this study, the synthesis of composite materials produced from Ni/Al with three types of carbon-based materials namely chitosan (Ch), cellulose (Ce), and graphene oxide (GO) was successfully carried out supported by X-ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FT-IR), and Brunauer-Emmett-Teller (BET) analysis. The combined characteristics of the two starting materials are present in the composite material based on XRD and FT-IR data. The surface area of Ni/Al-LDH increased after compositing with Ch, Ce, and GO, from 3.3 m2/g to 9.5 m2/g in Ni/Al-Ch, 5.1 m2/g in Ni/Al-Ce, and 78.4 m2/g in Ni/Al-GO. These findings indicate that the materials are suitable for various applications such as photocatalytic and adsorption as effective materials in further research.

Discrimination of Cheese Products Regarding Milk Species’ Origin Using FTIR, 1H-NMR, and Chemometrics

The present study deals with the discrimination of various European cheese products based on spectroscopic data and chemometric analysis. It is the first study that includes cheese products from Cyprus along with cheese samples from abroad and several different cheese types. Therefore, forty-nine samples were collected, freeze-dried, and measured by using spectroscopic techniques, such as FTIR (Fourier-Transform Infrared Spectroscopy) and 1H-NMR (proton nuclear magnetic resonance). Discriminant analysis was applied, particularly OPLS-DA. All data obtained from 1H-NMR were included, whereas, regarding the FTIR data, only the spectral subregion between 1900 and 400 cm−1 was used in the extracted model. The cheese samples were classified according to the milk species’ origin. In the future, the samples of this study will be enriched for further testing with spectroscopic techniques and chemometrics.

Physical characterization, magnetic interactions and DC electrical resistivity properties of La3+ substituted NiZnCd nano ferrites

In this article, we substituted La3+ ions to explore the structural, magnetic, and DC electrical resistivity properties of Ni0.5Zn0.4Cd0.1Fe2-xLaxO4 (x = 0.0, 0.02, 0.04, 0.06, and 0.08) nano-structured spinel ferrites. We employed X-ray diffraction (XRD), Field-emission scanning electron microscopy (FESEM) with Energy dispersive X-ray (EDX), Fourier transform infrared spectroscopy (FTIR), Vibrating sample magnetometry (VSM), and electrical measurements to characterize the studied samples, which were synthesized using the sol–gel auto-combustion process. XRD analysis confirmed that the prepared materials formed a single-phase nanostructure. Using Debye-Scherer's formula, we calculated the average crystallite size, which ranged from 29.01 to 21.52 nm. FESEM images demonstrated that each sample exhibited spherical nanocrystalline behavior. The variations of the prepared samples were confirmed constitutionally by EDX. The FTIR data revealed two absorption bands for all synthesized materials at υ1 = 562.18 to 590.51 cm−1 and υ2 = 410.18 to 430.51 cm−1, corresponding to the tetrahedral and octahedral sites of the spinel structure, respectively. Vibrant sample magnetometry spectra were utilized to investigate how La3+-doping affects the magnetic characteristics of NiZnCd ferrite. Due to enhanced La3+-doping, saturation magnetization, and coercivity values decreased. The La3+ doping of NiZnCd nano ferrites resulted in changes in saturation magnetization (from 83.66 to 69.57 emu/g), coercivity (from 33.75 to 60.51 Oe), and remanence magnetization (from 29.62 to 33.12 emu/g). These variations suggest the potential utility of the samples for magnetic recording and memory applications. The semiconducting behavior has been confirmed by the DC electrical resistivity measured values using a two-probe method. Data on DC electrical resistivity were also utilized to determine carrier concentration and activation energy, establishing a connection with La3+ replacement.

Ante- and Post-Mortem Fracture Identification Protocol Based on Low- and High-Level Fusion Using Fourier Transform Infrared Spectroscopy and Raman Spectroscopy Association.

In this study, the application of low-level fusion (LLF) and high-level fusion (HLF) strategies using a combination of Fourier transform infrared spectroscopy (FT-IR) and Raman spectroscopy in the identification of antemortem and postmortem fracture at different postmortem intervals (PMIs) was investigated. On a technical level, the same hard tissue sample can be detected using a mix of FT-IR and Raman techniques. At the method level, two cutting-edge chemometrics approaches (LLF and HLF) combining FT-IR and Raman spectroscopic data are explored. The models were ranked in accordance with their parametric quality as follows: HLF and LLF + HLF models > LLF single model > Raman single model > FT-IR single model. The LLF model performed marginally better than the Raman model, however, when compared to other models, the HLF model performed considerably better. The HLF model achieved the best performance, with both cross-validation accuracy and test data set accuracy of 0.88. The importance of the feature wavelengths in the model construction process was subsequently evaluated by intersection fusion, and it was found that the absorbance bands of amide I, PO43- ν1 ν3, and CH2 in FT-IR and phenylalanine, CO32- ν1- PO43- ν3, and amide III in Raman have outstanding contributions to the construction of antemortem and postmortem fractures identification models. Overall, the combination of FT-IR and Raman with the HLF strategy is a novel and promising approach for developing antemortem and postmortem fracture identification models at different PMIs.

Green Synthesis of Narrow-Size Silver Nanoparticles Using Ginkgo biloba Leaves: Condition Optimization, Characterization, and Antibacterial and Cytotoxic Activities.

Natural products derived from medicinal plants offer convenience and therapeutic potential and have inspired the development of antimicrobial agents. Thus, it is worth exploring the combination of nanotechnology and natural products. In this study, silver nanoparticles (AgNPs) were synthesized from the leaf extract of Ginkgo biloba (Gb), having abundant flavonoid compounds. The reaction conditions and the colloidal stability were assessed using ultraviolet-visible spectroscopy. X-ray diffraction, transmission electron microscopy, and Fourier transform infrared spectroscopy (FTIR) were used to characterize the AgNPs. AgNPs exhibited a spherical morphology, uniform dispersion, and diameter ranging from ~8 to 9 nm. The FTIR data indicated that phytoconstituents, such as polyphenols, flavonoids, and terpenoids, could potentially serve as reducing and capping agents. The antibacterial activity of the synthesized AgNPs was assessed using broth dilution and agar well diffusion assays. The results demonstrate antibacterial effects against both Gram-positive and Gram-negative strains at low AgNP concentrations. The cytotoxicity of AgNPs was examined in vitro using the CCK-8 method, which showed that low concentrations of AgNPs are noncytotoxic to normal cells and promote cell growth. In conclusion, an environmentally friendly approach for synthesizing AgNPs from Gb leaves yielded antibacterial AgNPs with minimal toxicity, holding promise for future applications in the field of biomedicine.

Degradation mechanisms of Indian banks promissory notes written in iron‐gall inks and its conservation

AbstractThe objective of this study is to investigate the deterioration of 18th‐century Indian Bank's Promissory Notes written using iron‐gall ink. The research employs non‐destructive techniques such as Fourier transform infrared spectroscopy (FTIR), X‐ray diffraction (XRD) and scanning electron microscopy (SEM) with energy‐dispersive X‐ray spectroscopy to analyze the elemental composition and structural characteristics of both the iron‐gall ink and the paper support. The analytical findings indicate that the acid hydrolysis of the iron‐gall ink complex has led to corrosion and weakening of the document. The reactivity of Fe3+ ions, indirectly assessed through XRD analysis by measuring the crystalline index (Crl) of the paper, indicates a loss of strength in the cellulose fibers. The combination of FTIR and XRD data also reveals the utilization of gypsum as a filler in the paper, likely intended to enhance its gloss and opacity. SEM photomicrographs further illustrate the presence of iron crystals on the paper surface, a result of the non‐uniform distribution of the ink and oxidation of ferrous ions also supported by surface mapping of iron. The paper's composition is identified as cellulose I, a common variety found in nature. These findings collectively provide insights into the degradation processes affecting both the iron‐gall ink and the paper support. The innovative calcium phytate treatment was applied for document conservation.

Synthesis, characterization, molecular docking, and cytotoxicity study of ruthenium (II/III) polypyridyl complexes

A new polypyridyl ligand 4‐(4‐nitrophenoxy)‐N,N‐bis (pyridin‐2‐ylmethyl)aniline (L1) and its three ruthenium (II/III) complexes, [Ru (Cl)3L1] (C1), [Ru(L1)2]Cl (C2), and [RuCl (dpa)L1] (C3) where dpa = 2,2‐dipyridylamine, have been successfully synthesized and characterized using Fourier‐transform infrared spectroscopy (FTIR), elemental analysis, proton nuclear magnetic resonance (1H NMR), high‐resolution electrospray ionization mass spectrometry (HR‐ESI‐MS), thermal analysis (thermogravimetric analysis [TGA] and differential scanning calorimetry [DSC]), UV/Vis absorption, and magnetic susceptibility. The structures of the ligand and the complexes were optimized, and the structural characteristics were determined by density functional theory (DFT) using the B3LYP‐GD3/6‐311G++(d,p) method. Optimized FTIR vibrational frequencies and 1H NMR chemical shifts agreed well with the corresponding experimental FTIR and 1H NMR data. In vitro cytotoxicity of the ligand and the complexes were evaluated against the MCF‐7 breast cancer cell line. Ligand L1 was the most potent with an IC50 of 38.45 μM, followed by C2 with an IC50 of 45.23 μM. However, the ligand and the complexes showed low antiproliferative activity compared to cisplatin, which had an IC50 of 9.67 μM. To predict the reactivity trend of L1 and the complexes, frontier molecular orbital (FMO) analysis was performed. The FMO energy gap (Eg = ELUMO − EHOMO) for C2 was found to be 1.675 eV, which was the lowest among all the complexes or L1. In addition, molecular docking studies were carried out so as to predict the binding capacity of L1 and the complexes to estrogen receptor alpha (ER‐α). The results showed that C2 has the most negative binding energy score (−9.63 kcal/mol), which indicates more stable adducts with the key amino acid residues at the active sites of ER‐α. Furthermore, C2 displayed the lowest inhibition constant (Ki) of 0.09 μM compared to all the complexes or L1. These results are very promising and show that the novel complex C2 may help in the development of anticancer drugs.

Dielectric analysis of surface modified nano-graphite: effects of frequency and thickness

The nano-graphite (NG) and acid modified nano-graphite (ANG) have been synthesized from graphite powder via mixture of strong acid (sulphuric acid and nitric acid) respectively by a soft chemistry route involving microwave, ultrasonic method and characterized by high-resolution electron microscopy (HR-TEM), scanning electron microscopy (SEM), fourier-transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD), clearly demonstrated the successful synthesis of acid modified NG. SEM images confirmed the surface morphology of NG, and ANG and HR-TEM study shows the nanoparticles size of NG and ANG. FTIR data confirmed the presence of acid functional groups on the surface of synthesized NG powder. XRD data of NG and ANG shows that 2θ is at 26.43° and 0.336 nm is an interlayer distance (d). NG and ANG pellets have been prepared for their dielectric analysis with frequency for different thickness. The dielectric loss tangent (tanδ) spectra show relaxation peak with frequency and peak shifts due to presence of polar groups in the ANG. The capacitance values of NG and ANG decrease with frequency and increase with thicknesses due to the capacitive nature of nanoparticles. The dielectric permittivity decreases with frequency and increases with thickness due to the charge orientation and dipole moment change of functional groups of synthesized NG, and ANG. The electrical conductivity of NG and ANG nanoparticles increases with frequency and thickness of NG and ANG pellets due to the conductive nature. Electrical conductivity and dielectric permittivity of NG and ANG are found to highly rely on thickness, according to the dielectric evaluation.

In Situ Synthesis of Polyaniline Nanohybrid and Formulation of Polyaniline/ Carboxymethyl cellulose/Ethylene Glycol Nanocomposite: Study of its Conducting and Antibacterial Properties

Polyaniline (PANI) has received great attention as a conducting polymer from researchers in the field of organic synthesis and development of conducting nanocomposite polymer technology for superconductors. Different methods of PANI synthesis are being sought for the obtainment of electrically robust PANI composites for electronic and other useful applications. Different inorganic matrices have been considered for this purpose. This study attempts to prepare PANI In situ on arginine-modified nanoclay template by chemical oxidation polymerization. Further, the PANI/Arginine-modified nanoclay was used to prepare PANI/Arginine-Nanoclay/Carboxymethyl cellulose/Ethylene glycol conducting film with robust electric conductivity (EC). Electrical conductivities, anti-bacterial evaluation, Fourier-transform infrared spectroscopy (FT-IR), thermogravimetry analysis (TGA), differential thermogravimetry analysis (DTG) and Scanning Electron Microscopy (SEM) were used for the characterization studies and property evaluation. The electrical conductivities of PANI/Arginine-Nanoclay/Carboxymethyl cellulose/Ethylene glycol nanocomposite film reached 1900 S/Cm. FT-IR data, 3304–3196, 2926–2828, 2200–2022, 1733, 1620 and 1052 cm-1 respectively, confirmed the presence of organic intercalates, CMC, quinoid and benzenoid rings of PANI, and the inorganic nanoclay matter in the nanocomposite film. SEM revealed the presence of spine-like nanoflowers with elongated and expanded particle agglomerations. Thermal stability of the prepared nanocomposite thin film reached 700oC. The zone of inhibition ranged from 24-36 mm against S. typhi, E. coli and S. aureus. In conclusion, PANI nanocomposite thin conducting films had robust EC and antibacterial properties. In addition, the In-situ synthesis of PANI on Arginine-modified nanoclay platform aided the electric conductivity of the nanocomposite system.

Unleashing the power of SAN: Innovative in situ fibrillation and moisture-crosslinking techniques yield stronger, tougher, and Greener material than ABS

Styrene-acrylonitrile (SAN) is widely used in various applications due to its excellent properties, including thermal stability, dimensional stability, and chemical resistance. However, poor toughness has limited its applications. In this study, an innovative in-situ fibrillation technique was employed to create nanofibers of thermoplastic polyurethane (TPU) in the SAN matrix. Silane was initially grafted onto TPU, followed by the development of nanofibril TPU, and lastly, post-crosslinking was conducted to retain the nanofibril structure. The grafting reaction was analyzed using Fourier Transform Infrared Spectroscopy (FTIR) and Proton Nuclear Magnetic Resonance Spectroscopy (1H NMR). FTIR and NMR data were used in conjunction with the gel content test to confirm the involved grafting, hydrolysis, and crosslinking reactions. Observations with a Scanning Electron Microscope (SEM) revealed the formation of nanoscale TPU fibers ranging from 90 to 360 nm for various TPU contents. Because of nanofibril TPU's high aspect ratio and the effective SAN-TPU interaction, the required TPU decreased to 1 wt%. Due to the minimal use of rubber, SAN's stiffness was not compromised and compared to pure SAN and a spherical structure with the same concentration, tensile toughness increased by 350% and 200%, respectively. The fracture mechanism was investigated for both the short and long timeframes of deformation, and several potential hypotheses were proposed. Finally, this novel toughened SAN was compared with one of the most effective toughened acrylonitrile butadiene styrene (ABS) materials that contain 40 wt% spherical butadiene rubber (BR) domains.

Phytochemical composition, anti-amylase and anti-acetylcholinesterase activities of leaf extracts and herbal tea of Dolichandrone serrulata (DC.) seem

The number of elderly population is continually growing in Thailand. Major health problems mostly occurred in the elder are non-communicable diseases namely Alzheimer's disease and type 2 diabetes mellitus. In current study, phytochemical composition, anti-amylase and anti-acetylcholinesterase activities of leaf extracts and herbal tea from Dolichandrone serrulata (DC.) Seem were determined. The result showed that extracts and herbal tea samples of D. serrulata leaves had effective in inhibition of amylase (an effective concentration at half maximum (EC50) = 1.21 to 23.80 mg/ml) and acetylcholinesterase activities (EC50 = 2.63 to 49.55 mg/ml). The effect of infusion time on the inhibition of amylase indicated that the best infusion time for preparing herbal tea beverage was 3 min, while the inhibition of acetylcholinesterase was 5 min. The fourier transform infrared spectroscopy (FTIR) and gas chromatograph - mass spectrometer (GC–MS) data indicated the presence of phytochemicals in the extracts and herbal tea samples related to phenolic compounds and flavonoids. The principal component analysis (PCA) result from FTIR data could discriminate herbal tea samples from the ethanol and aqueous extracts better than the PCA biplot of anti-amylase activity and anti-acetylcholinesterase activity.

Cinnamon-based rapid biosynthesis of silver nanoparticles; its characterization and antibacterial properties

The development of nanotechnology is generating interest of researchers towards the alternative synthesis procedures of metal nanoparticles that may be employed in various applications like drug delivery, photo-electrochemical devices, diagnostic techniques, antimicrobial sanitizers, sunscreens, single-electron transistors, nano-engineered solar cells, etc. Thus, green synthesis of metal nanoparticles is becoming an attractive method for obtaining particles with nano-scale. The biosynthesized AgNPs were characterized using UV–Visible spectroscopy, X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM), and energy-dispersive X-ray analysis (EDX). The UV–Visible spectrum showed a characteristic absorption peak for Ag at around 420–440 nm with optical bandgaps of about 3.42 eV–3.33 eV of AgNPs. XRD patterns at (111), (020), (022), (131), and (222) lattice planes depicted the production of face-centered cubic silver nano-structure with approximate crystal size ranges from ≈20 to 50 nm by Scherrer’s formula. The FTIR data indicated the presence of active biomolecules responsible for stabilization in the AgNPs structure. We reported the antibacterial properties of silver nanoparticles (AgNPs) derived from cinnamon bark extract against Salmonella typhimurium, Pseudomonas aeruginosa, Staphylococcus aureus, and Escherichia coli. This study on AgNPs might be a promising approach suggesting alternative treatment methods against pathogenic bacteria in the field of medicine.

Spectroscopic Analyses Highlight Plant Biostimulant Effects of Baker's Yeast Vinasse and Selenium on Cabbage through Foliar Fertilization.

The main aim of this study is to find relevant analytic fingerprints for plants' structural characterization using spectroscopic techniques and thermogravimetric analyses (TGAs) as alternative methods, particularized on cabbage treated with selenium-baker's yeast vinasse formulation (Se-VF) included in a foliar fertilizer formula. The hypothesis investigated is that Se-VF will induce significant structural changes compared with the control, analytically confirming the biofortification of selenium-enriched cabbage as a nutritive vegetable, and particularly the plant biostimulant effects of the applied Se-VF formulation on cabbage grown in the field. The TGA evidenced a structural transformation of the molecular building blocks in the treated cabbage leaves. The ash residues increased after treatment, suggesting increased mineral accumulation in leaves. X-ray diffraction (XRD) and Fourier-transform infrared spectroscopy (FTIR) evidenced a pectin-Iα-cellulose structure of cabbage that correlated with each other in terms of leaf crystallinity. FTIR analysis suggested the accumulation of unesterified pectin and possibly (seleno) glucosinolates and an increased network of hydrogen bonds. The treatment with Se-VF formulation induced a significant increase in the soluble fibers of the inner leaves, accompanied by a decrease in the insoluble fibers. The ratio of soluble/insoluble fibers correlated with the crystallinity determined by XRD and with the FTIR data. The employed analytic techniques can find practical applications as fast methods in studies of the effects of new agrotechnical practices, while in our particular case study, they revealed effects specific to plant biostimulants of the Se-VF formulation treatment: enhanced mineral utilization and improved quality traits.