Fourier Transform Infrared Spectra Research Articles

Chlorine Dioxide Delays Enzymatic Browning in Postharvest Cherimoya and Enables Establishment of Kinetics Substrate Model

Cherimoya (Annona squamosa L.) is a nutrient-rich fruit. However, it is not easy to store because of its susceptibility to browning. In order to prolong the storage period of cherimoya, the fruit was treated with chlorine dioxide (ClO2) at different concentrations (20, 40, 60, 80, and 100 mg L−1) and stored at 15 °C for 8 days. The quality and biochemical indexes of the fruit were investigated using a chromameter, high-performance liquid chromatography and scanning electron microscopy, etc. The results showed that all the treatments with various concentrations of ClO2 could delay the increase in the browning index, loss of weight, and decrease in hardness. Meanwhile, ClO2 treatment effectively reduced the consumption of starch, titratable acids, and phenolics as well as inhibited the polyphenol oxidase (PPO) activity and enzymatic oxidation. It can be seen from the Fourier transform infrared spectrum (FTIR) that the C=O stretching peak at 1731 cm−1 disappeared at a ClO2 concentration of 60 mg L−1. We think the ClO2 treatment may inhibit the oxidation of phenol to quinone. According to the Arrhenius formula, the values of the apparent activation energy (Ea) for enzymatic browning reaction were estimated. The Ea with catechol in cherimoya pericarp and flesh were 67.00 and 47.83 kJ mol−1, respectively. It was found that the phenolic enzyme reaction with catechol has a much smaller Ea and a higher affinity for PPO. Therefore, treatment with ClO2 at a suitable concentration for cherimoya stored at 15 °C could effectively maintain fruit quality and prolong the storage period; the most appropriate concentration is 60 mg L−1.

Synthesis and characterization of MoS2-COOH /Co composite as electrode material for Asymmetric supercapacitors (SCs) and devices

Transition Metal Dichalcogenide (TMD) supercapacitors have garnered significant interest due to their considerable potential. Contributing to the advancements in this field, our study focuses on the first successful synthesis of nanoparticle Co-doped MoS2-COOH using a hydrothermal approach. We examine its performance in electrochemical applications, specifically as an electrode for a supercapacitor. The MoS2-COOH/Co composite was characterized using various techniques, including X-Ray diffraction (XRD), Fourier-transform infrared spectrum (FTIR), scanning electron microscopy (SEM), energy-dispersive X-ray (EDX) spectroscopy, adsorption–desorption isotherm, and thermogravimetric analysis (TGA). The supercapacitive characteristics of MoS2-COOH/Co composite in a 1 M KCl electrolyte were analyzed through cyclic voltammetry (CV), continuous current charge-discharge cycling (CD), and electrochemical impedance spectroscopy (EIS). Following 3000 charge-discharge cycles, the MoS2-COOH/Co electrode, constructed on Ni foam, exhibited a unique capacitance of 2500 F g−1 with a cyclic retention of 85 % at a density of 20 mA cm−2. The synthesized material demonstrated excellent electrochemical performance for supercapacitor applications, as evidenced by Nyquist and Bode phase angle results.

Green Synthesis of Iron Nanoparticles (FeNPs) using Aqueous Extract of Murraya koenigii Leaves: Synthesis Mechanism, Characterization Process and Antibacterial Activity

Introduction: Green synthesis is the method of producing metal and metal oxide nanoparticles from the extraction of plant materials. This study aims to synthesize iron nanoparticles (FeNPs) using an aqueous extract of Murraya koenigii leaves as an eco-friendly approach and subsequently characterize the synthesized FeNPs to understand their structural, morphological, compositional and optical properties. Methods: The aqueous extract of Murraya koenigii leaves and 0.1M ferric chloride solution were combined at room temperature in a 1:2 volume ratio. The synthesized FeNPs were characterized using analysis methods of Scanning Electron Microscope (SEM), Energy Dispersive X-ray (EDX), X-ray diffraction (XRD), Fourier Transform Infrared (FTIR), UV-visible (UV-vis) and Tacu plot. Results: SEM images discovered that the particles were in the nanoscale range and their morphology appeared spherical shape. The EDX study was used to identify the composition of the elements of synthesized FeNPs. The crystal structure of the synthesised FeNPs was shown in the XRD spectrum. The FTIR spectrum showed many distinctive bands and the bands revealed active components for functional groups in the synthesized FeNPs. The UV-vis spectrum revealed an absorbance peak range of 240-310 nm for FeNP formation with a maximal peak at 273 nm. The band gap energy of the synthesized FeNPs was found to be 2.07 eV using the Tauc plot method. Also, the synthesized FeNPs exhibited a significant antibacterial effect against bacterial pathogens. Conclusion: The results of the characterization methods strongly suggest that the aqueous leaf extract of Murraya koenigii can be used as a reducing and stabilizing agent in the green synthesis of FeNPs.

Enhancing early identification of high-fertile cattle females using infrared blood serum spectra and machine learning

Artificial insemination (AI) success in bovine reproduction is vital for the cattle industry’s economic sustainability and for advancing the understanding of reproductive physiology. Identify high-fertile animals’ fertility is a complex task due to multifactorial traits, including hormonal, age-related, and body condition factors. Early high-fertility identification is crucial for timely interventions and enhancing AI success. In this study, we present the potential use of Fourier-transform infrared (FTIR) spectroscopy on blood serum for early identification of high-fertile Nellore female cows for AI protocols. Blood serum FTIR spectra were obtained from Nellore female cows before AI. FTIR spectra underwent data analysis and the results demonstrated successful discrimination between animals that exhibit pregnant and non-pregnant diagnoses 30 days after AI. FTIR spectra revealed consistent vibrational modes, emphasizing Amide I and II bands. Principal Component Analysis (PCA) effectively segregated groups based on molecular information. Linear SVM with C = 10 and 4 PCs achieved 100% accuracy in the group classification. This innovative approach using FTIR spectroscopy and ML algorithms offers a promising means of high-fertile cow identification, potentially improving AI outcomes in Nellore cattle. The study presents valuable insights into advancements in reproductive management practices for this economically significant breed.

Fourier-Transform Infrared Spectral Library of MXenes.

Fourier-transform infrared (FTIR) spectroscopy characterization is a powerful and easy-to-use technique frequently employed for the characterization and fingerprinting of materials. Although MXenes are a large and fastest growing family of inorganic 2D materials, the lack of systematic FTIR spectroscopy studies hinders its application to MXenes and often leads to misinterpretation of the results. In this study, we report experimental and calculated FTIR spectra of 12 most typical carbide and carbonitride MXenes with different compositions (5 transition metals) and all four basic structures, including Ti2CT x , Nb2CT x , Mo2CT x , V2CT x , Ti3C2T x , Ti3CNT x , Mo2TiC2T x , Mo2Ti2C3T x , Nb4C3T x , V4C3T x , Ta4C3T x , and Mo4VC4T x . The measurements were performed on delaminated MXene flakes incorporated in KBr pellets in the 4000-400 cm-1 range. We provide detailed instructions for sample preparation, data collection, and interpretation of FTIR spectra of MXenes. Background correction and spectra smoothing are applied to obtain clear FTIR peaks corresponding to bond vibrations in MXenes. Density functional theory calculations were used for the precise assignment of all characteristic FTIR peaks and an in-depth analysis of the vibration modes. This work aims to provide the 2D material community with the FTIR spectroscopy technique as a reliable method for identifying and analyzing MXenes.

Synthesis, characterization and correlation studies on the Ni–Zn–Mn ferrite as a photocatalyst

Samples of Ni0.3Zn0.7−xMnxFe2O4 (x = 0, 0.15, 0.25, 0.35, 0.45, 0.55) nanoparticles (NPs) were synthesized by auto-combustion flash method. These ferrites were used as catalysts for photodegradation of methylene blue (MB) dye utilizing visible light energy. Structural analysis was carried out using the X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy, while nanoparticle dimensions were elucidated through transmission electron microscopy (TEM). The magnetic and optical behaviours were unveiled via vibrating sample magnetometer and UV–VIS spectroscopy, respectively. The XRD outcomes established the presence of a cubic spinel-type structure for the studied ferrite samples. The FTIR spectra unveiled two absorption characteristic bands of the spinel ferrite. TEM images revealed nanoscale dimensions of ferrite NPs with the range from 21.1 to 51.8 nm. The optical features exhibited an indirect band gap energy spanning from 4.25 to 4.36 eV. Magnetization behaviour displayed a sinusoidal trend corresponding to varying Mn concentrations. The ferrite NPs catalyst (10 mg) yield photodegradation efficiency ranged from 22.8 to 33.9% for 100 ml MB dye solution after 120 min of light irradiation. The effects of dye concentration and catalyst dose on the degradation efficiency were examined using the Ni0.3Zn0.35Mn0.35Fe2O4 catalyst with highest degradation (= 33.9%). On the other hand, the dependence of the degradation efficiency on the structure, morphological, magnetic and optical properties of the photocatalyst was investigated. The findings of this study underscore the potential of the prepared ferrite nanoparticles for advanced applications in environmental restoration.Graphical abstract

Alocasia Indica Assisted Green Synthesis of Metallic Cu Nanoparticles for Enhanced Antimicrobial Activities

In the past several years, the widespread utility of copper nanoparticles (CuNPs) has spurred global interest in streamlining synthesis methodologies. Notably, this study introduces an environmentally conscious strategy for synthesizing CuNPs using the extract of Alocasia indica. Employing a chemical reduction process, A. indica, abundant in phenolics and flavonoids, acts as a potent reducing agent. The nanoparticles (NPs) synthesized by A. indica have been carefully characterized by Ultraviolet–Visible (UV–Viz) spectroscopy, Fourier Transform Infrared (FTIR) spectroscopy, Scanning Electron Microscopy (SEM), Energy Dispersive X-ray (EDX), Transmission Electron Microscopy (TEM), X-ray Diffraction (XRD) analysis and antimicrobial analysis. UV testing, spanning wave length, elucidates light absorption attributed to the newly formed CuNPs by showcasing a surface plasmonic resonance peak at 204 nm. The evolution of the FTIR spectrum of the produced CuNPs confirms the presence of diverse biomolecules. TEM delineates the synthesis of irregularly shaped particles. Elemental composition analysis via EDX identifies the presence of various elements, including C, O, Al, Cl, K and Cu, with detailed insights into their mass percentages, standard deviations, atom percentages and characteristic X-ray energy levels. The successful synthesis of CuNPs is validated by XRD, which reveals characteristic copper peaks at 2[Formula: see text] = [Formula: see text], [Formula: see text] and [Formula: see text]. The synthesized NP showed 98.99% inhibition against Staphylococcus aureus and 99.99% inhibition against Escherichia coli. This research presents an easy, economical and ecologically friendly process for producing CuNPs utilizing A. indica extracts.

Trehalose–whey protein conjugates prepared by structural interaction: Mechanisms for improving the multilevel structure and their water solubility and protein digestibility

Whey proteins (WPs) are the most widely used protein supplements worldwide. This study investigates the impact of incorporating trehalose into WPs at different ratios ranging from 1% to 5% (w/v) on the structural characteristics, surface properties, and functionality of trehalose (T) conjugated to WPs (T-WP). The T-WP conjugate was produced using the pH-shifting technique. Our findings demonstrated that conjugating trehalose into WPs significantly altered the Fourier-transform infrared (FTIR) spectrum, tertiary structure, and protein conformation. The surface charge and hydrophobicity of T-WPs were changed significantly (p < 0.05). Structural modifications had a notable effect on the solubility and digestibility of T-WPs. The water solubility of T-WPs increased from 88.12% to 95.53% when conjugated with 5% (w/v) trehalose. Furthermore, the impact of the development of T-WPs on FTIR spectrum was investigated. The β-sheet, random coil, α-helix, and β-turn were changed significantly from 36.17% to 45.21%, 12.38% to 16.39%, 10.69% to 13.44%, and 40.76% to 24.94%, respectively. The results presented in this study offer structural information to enhance the creation of WP products with improved functional properties.

Adsorptive removal of a nitrate ion from the aqueous solution of sodium nitrate by application of double fixed-bed column

This study focuses on the removal of nitrate ions from aqueous solutions using rice husk activated carbon (RHAC). The RHAC was subjected to characterization via Fourier transform infrared (FTIR), scanning electron microscopy coupled with energy dispersive spectroscopy (SEM-EDS), and X-ray florescence (XRF) to ascertain its functional groups, surface morphology, and oxide/elemental composition, respectively. Batch experiments were conducted to assess the impact of nitrate concentration, bed height, and number of packing layers on removal efficiency. FTIR spectra revealed favorable sorption-related functional groups within RHAC, while SEM analysis indicated the presence of effective sorption sites on its surface. EDS analysis of the rice husk adsorbent before adsorption (RHBS) demonstrated a significant composition of Si (42.20%), O (35.30%), and Ca (12.33%). The batch study unveiled a concentration-dependent decrease in nitrate removal efficiency, alongside the enhanced performance with increased bed height and number of packing layers. Kinetic data fitting favored the Yoon–Nelson and Adams–Bohart models. Overall, RHAC exhibited efficient nitrate ion removal, with column performance notably improved by utilizing multiple packing layers. These results will enhance our understanding of the mechanisms involved in removing nitrate ions and highlight the potential effectiveness of RHAC, especially when utilized with multiple packing arrangements in column setups.

Zein film loaded with Fructus Ligustri Lucidi essential oil: Preparation, characterization and application in fresh-cut apple preservation

Fresh-cut fruits and vegetables are a type of convenient, ready-to-use food that offers consumers a healthy choice. However, the peeling and slicing operations make them susceptible to microbial contaminations and oxidation. In this study, zein was used as the film-forming substrate, and Fructus Ligustri Lucidi essential oil (FEO), a natural bacteriostatic agent, was incorporated into zein film to prepare a film with antibacterial and antioxidant properties to prolong the shelf life of fresh-cut fruits and vegetables. Polyethylene glycol 400 (PEG400) and glucose were used as plasticizers, and the optimal formulation of the film (FZF) was obtained by orthogonal experiment: 10% PEG400, 5% glucose and 10% FEO. The films were characterized by scanning electron microscope (SEM), Fourier transform infrared spectrum (FTIR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA), and the influence of FEO on the physical, chemical, and biological characteristics of the films was explored. The results demonstrated that FEO was successfully loaded into zein film and distributed evenly. The FZF film exhibited excellent antioxidant activity, when the concentration of FEO was 200 μg/mL, the scavenging rate of DPPH and ABTS was 81.63 ± 0.69% and 91.44 ± 0.55% respectively. Furthermore, the FZF film showed antibacterial properties against Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) and low cytotoxicity in vitro. Moreover, the FZF film demonstrated anti-browning capabilities, effectively prolonging the shelf life of fresh-cut apple slices. Thus, the FZF film possesses considerable potential for utilization in food packaging.

Synthesis of Calcium Carbonate from Orange Peel Waste Extract: A Mechanistic Investigation

The present work reports the mechanism and synthesis of calcium carbonate (CaCO3) formation from orange peel, which is one of the most common agriculture waste generated throughout the globe. The zest of oranges was co-distilled with distilled water to separate the essential oil content. Further, the residue was washed twice with distilled water to get the desired extract. For the green synthesis of CaCO3, a saturated solution of calcium nitrate tetrahydrate (Ca(NO3)2·4H2O) was mixed thoroughly with orange peel extract in the 1:3 proportion. This solution was kept on magnetic stirrer while maintaining temperature at 85˚C, heated at 100˚C for 13 h which was further annealed at 300˚C, 500˚C and 700˚C. X-ray diffraction (XRD) shows the presence of calcite phase corresponding to CaCO3. Fourier transform infrared spectra (FTIR) exhibits the bands corresponding to Ca-O, C-O and vibrations of CO3-2 bonds whereas UV–Visible spectroscopy shows the optical behavior of CaCO3. The qualitative analysis of orange peel extract as well as the black-brown gel formed as a result of sol–gel synthesis method was examined using Gas Chromatography & Mass Spectrometry (GCMS). It revealed the presence of acidic groups (2,3-butanediol & 1,4-benzenediol) which led to the development of a mechanism, governing the formation of CaCO3.

Green synthesis and characterisation of silver nanoparticles utilising a bioflocculant obtained from Pichia kudriavzevii isolated from kombucha tea SCOBY

ABSTRACT A Pichia kudriavzevii produced bioflocculant was used in the biosynthesis of silver nanoparticles (AgNPs). The generated Ag nanoparticles were given several analytical treatments to determine their properties. These techniques included transmission electron microscope (TEM), energy-dispersive X-ray spectroscopy (EDX), Fourier-transform infrared (FT-IR), transmission electron microscopy (TEM), scanning electron microscope (SEM), X-ray diffraction spectroscopy (XRD), thermogravimetric analysis (TGA), and UV–vis spectroscopy. The SEM scans showed particles that were smooth and nearly spherical in shape. EDX analysis showed the element silver with a percentage weight of 61.93% in addition to the elements present in the bioflocculant. Through FT-IR spectra functional groups for instance carboxyl, polyphenols, aromatics, alcohol, amine, and halo compounds were observed. The TEM picture displayed spherical particles that had a size range between 7 and 12 nm. TGA analysis revealed that AgNPs are thermally stable with over 85% mass retained at high temperatures, while the bioflocculant retained 60% weight after exposure to higher temperatures. UV–visible spectroscopy revealed an SPR band at 450 nm, while X-ray diffraction showed a crystallite size of 19 nm. Utilising bioflocculant as stabilising and coating agents in the biosynthesis of AgNPs is an ecologically safe technique that offers synthesis rates that are quicker and on par with chemical methods.

FTIR study of light-induced proton transfer and Ca2+ binding in T82D mutant of TAT rhodopsin

Proton transfer reactions play important functional roles in many proteins, such as enzymes and transporters, which is also the case in rhodopsins. In fact, functional expression of rhodopsins accompanies intramolecular proton transfer reactions in many cases. One of the exceptional cases can be seen in the protonated form of marine bacterial TAT rhodopsin, which isomerizes the retinal by light but returns to the original state within 10−5 s. Thus, light energy is converted into heat without any function. In contrast, the T82D mutant of TAT rhodopsin conducts the light-induced deprotonation of the Schiff base at high pH. In this article, we report the structural analysis of T82D by means of difference Fourier transform infrared (FTIR) spectroscopy. In the light-induced difference FTIR spectra at 77 K, we observed little hydrogen out-of-plane vibrations for T82D as well as the wild-type (WT), suggesting that the planar chromophore structure itself is not the origin of the reversion from the K intermediate in WT TAT rhodopsin. Upon relaxation of the K intermediate, T82D forms the following intermediate, such as M, whereas K of WT returns to the original state. Present FTIR analysis revealed the proton transfer from the Schiff base to D82 in T82D upon formation of the M intermediate. It is accompanied by the second proton transfer from E54 to the Schiff base, forming the N intermediate, particularly in membranes. The equilibrium between the M and N intermediates corresponds to the protonation equilibrium between E54 and the Schiff base. We also found that Ca2+ binding takes place in T82D as well as WT but with 6 times lower affinity. An altered hydrogen-bonding network would be the origin of low affinity in T82D, where deprotonation of E54 is involved in the Ca2+ binding.

Spectral analysis and characterization of Na2O-SiO2-ZrO2 glasses doped with V2O5

Na2O-SiO2-ZrO2 glasses doped with V2O5 were prepared with the melt quenching method, and were then analyzed using various techniques; in particular, with X-ray diffraction (XRD), energy dispersive spectroscopy (EDS), and optical absorption, photoluminescence, electron spin resonance (ESR), and Fourier transform infrared (FT-IR) transmission spectroscopy. The obtained results indicate that, in the studied glasses, vanadyl complexes tend to undergo a reduction from V5+ ions to V4+ ions. XRD and EDS data suggest that the glasses have amorphous nature with randomly distributed grains within the glass matrix. The optical absorption spectra show two transitions: 2B2g→2B1g and 2B2g→2Eg. The photoluminescence spectra exhibit a broad band from 750-900 nm, indicating the 2E→2T2 transition of vanadyl ions. The energies of the band gaps decreased gradually with increasing V2O5 content. The ESR spectra suggest that V4+ ions are situated in octahedral sites with tetragonal compression. The FT-IR spectra confirm the presence of various structural units within the glasses. Finally, the dielectric properties of the glasses were also measured, showing that the dielectric constant (ε′) and the loss tangent (tan δ) increase as the content of vanadium ions increases, indicating presence of V4+ ions within the glass matrix.

Reutilization of post-adsorption lanthanum-loaded straw alleviates phosphorus pollution in rice-wheat system: Subsequent performance and underlying mechanisms

Adsorption technology for phosphorus (P) removal is considered promising and reutilization of post-adsorbent can contribute to promoting sustainable agricultural production. However, the long-lasting impact of the post-adsorbent on crop growth and P remains unclear. This study assessed the effects of P-adsorbed lanthanum-modified straw (La@straw-P) on the rice yield, P fractionation and associated water quality parameters. The findings indicated that, compared with traditional fertilizer regimes, La@straw-P expedited the P reduction in the flooding water achieving a rate of decline to the tertiary standard for surface water (0.20 mg/L) 3.8 times faster and enhanced increased the P harvest index by 17.00 %. Economic estimation proved the positive benefits of La@straw-P in planting-breeding combination system. Redundancy analysis (RDA) and co-occurrence network analysis (CONA) revealed that electrical conductivity (EC) and dissolved Fe played primary roles in regulating total P. Fourier transform infrared spectra (FTIR), X-ray diffraction (XRD), X-ray photoelectron spectra (XPS), and soil P fractions collectively demonstrated that the abundant adsorption sites on La@straw-P could facilitate the transformation of active P into moderately Ca-bound P. This study proposes a strategy for recycling P-adsorbed materials to mitigate agricultural non-point P pollution.

Tagetes erecta-Mediated Biosynthesis of Mn3O4 Nanoparticles: Structural, Electrochemical, and Biological Investigations.

Mn3O4 nanoparticles (NPs) find diverse applications in the fields of medicine, biomedicine, biosensors, water treatment and purification, electronics, electrochemistry, and photoelectronics. The production of Mn3O4 NPs was reported earlier through various physical, chemical, and green routes, but no studies have still been performed on their biosynthesis from Tagetes erecta. We synthesized manganese oxide NPs, i.e., (Mn3O4)L and (Mn3O4)P NPs, by utilizing leaves and petals, respectively, of T. erecta as reducing and stabilizing agents. The investigated green path is eco-friendly and does not involve any hazardous raw materials. The structural properties of NPs were determined by X-ray diffraction (XRD) analysis, spectroscopies (Fourier transform infrared (FTIR), Raman, and UV-visible), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). The NPs were also evaluated for their electrochemical properties by cyclic voltammetry (CV) and galvanostatic charge-discharge (GCD). XRD analysis was performed to verify their tetragonal geometry, and the crystallite size (19.24 nm) of (Mn3O4)P was smaller than that (20.84 nm) of (Mn3O4)L NPs. SEM images displayed a porous and spherical morphology with a diameter of 14-35 nm. FTIR spectra of (Mn3O4)L and (Mn3O4)P displayed Mn-O vibrations at 605.69 and 616.87 cm-1, respectively, and the hydrous nature of the material. Raman spectroscopy revealed the existence of tetrahedral and octahedral units along with A1g, T2g, and Eg active modes of Mn3O4 and 2TO mode. UV-visible analyses of (Mn3O4)L and (Mn3O4)P NPs showed absorption peaks at 272.3 and 268.8 nm, along with band gaps of 4.83 and 5.49 eV, respectively. TGA curves displayed good thermal stabilities up to 600 °C and a loss of moisture content. DSC curves exhibited exothermic/endothermic peaks with glass transition temperatures of 258.9 and 308.7 °C for (Mn3O4)P and (Mn3O4)L, respectively. The CV curves showed redox peaks and confirmed that the electrochemical reaction takes place in the Mn3O4 material. GCD scans revealed the capacitive behavior of NPs and their suitability as electrodes in energy storage devices. However, (Mn3O4)L will act as a good material for energy storage applications as compared to (Mn3O4)P NPs. The synthesized NPs were also tested for their antibacterial efficacy by biofilm inhibition and agar well diffusion methods. The NPs showed higher activities against Staphylococcus aureus (Gram-positive) than against Escherichia coli (Gram-negative), and (Mn3O4)P was more bioactive than (Mn3O4)L.

Evaluation of spectroscopic techniques for on-site drug testing of festival seizures.

Despite the fact that drugs of abuse are illegal, a drug-free festival still remains an utopia in most settings. For law enforcement purposes, it is necessary to rapidly determine whether controlled substances are involved. On-site testing is a challenging task because drugs appear in different physical forms and concentrations. The aim of this study was to compare the performance of two spectroscopic techniques, Raman and Fourier transform-infrared (FT-IR), for the testing of drug seizures at a dance festival. First, samples were measured through packaging with Raman. Subsequently, homogenized samples were analysed with FT-IR. For MDMA tablets, a chemometric model was applied on the FT-IR spectra for the dose estimation. After the festival, results were confirmed in the forensic laboratory with gas chromatography coupled with mass spectrometry (GC-MS) and gas chromatography with flame ionization detection (GC-FID). In total, 166 samples of which 90 tablets, 53 powders, 16 crystals and 7 liquids were analysed. MDMA, cocaine and ketamine were the top three drugs seized. The Raman technique was suitable for powders and crystals (sensitivity of 100% and 81%, respectively). However, in comparison with FT-IR, Raman performance was lower for the analysis of liquids (sensitivity of 67%) and 'ecstasy'-like tablets (sensitivity of 41%). Overall, sensitivities above 95% were obtained with FT-IR. The MDMA doses of the tablets, determined on-site, ranged between 52 mg and 336 mg MDMA hydrochloride. For a quick identification of a variety of drugs on-site, the combination of Raman and FT-IR is recommended. It should be emphasized that optimized settings, in-house libraries and analysis by trained operators are essential to obtain correct results.

Photocatalyst based on composite of trimetallic metal-organic frameworks for efficient visible-light degradation in pharmaceutical pollutants abatement and process modeling using RSM

In this study, the facile synthesis of both monometallic Co- Metal-Organic Frameworks bimetallic Ni-Co-Metal-Organic Frameworks and trimetallic Ni-Co-Cu-Metal-Organic Frameworks was successfully accomplished with the chelation method. The prepared samples were characterized by using X-ray diffraction (XRD), field emission-scanning electron microscopy (FE-SEM), N2 adsorption–desorption, Fourier transform infrared spectra (FTIR), differential reflectance spectroscopy (UV–vis-DRS), and photoluminescence (PL) techniques was undertaken to examine the physicochemical attributes of the synthesized composites. The photocatalytic efficiency of the antibiotic ceftazidime(CAZ) degradation was investigated under visible light irradiation in 100 min. Kinetic studies revealed a pseudo-first-order model (50.0143, 0.009, and 0.0057 min−1 for Co-MOF, Co-Ni-MOF, and Co-Ni-Cu-MOF, respectively). Response surface methodology (RSM) demonstrated satisfactory predictability for CAZ degradation efficiency. Under optimized conditions (pH 10, 0.25 g L−1 catalyst) more than 97.38 % for the 20.0 mg L−1 of CAZ was degraded. Furthermore, the recyclability and scavenging test for the catalyst was evaluated.

Synergistic Effects of Pea Protein on the Viscoelastic Properties of Sodium Alginate Gels: Findings from Fourier Transform Infrared and Large-Amplitude Oscillatory Shear Analysis

The rheological characteristics of pea protein (PP100%) and alginate (AG100%) as pure and mixed gels with different levels of pea protein (AP90:10, AP80:20, and AP70:30) were investigated via large-amplitude oscillatory shear (LAOS) and Fourier transform infrared (FTIR). Small-angle oscillatory shear (SAOS) was carried out for the samples, and a slight frequency dependence of the storage modulus (G′) and the loss modulus (G″) was observed for the pastes and gels, indicating the formation of a weak network, which is crucial for understanding the gel’s mechanical stability under small levels of deformation. Elastic and viscous Lissajous curves from the LAOS measurement at different levels of strain (1 to 1000%) elucidated that the mixed gels formed a strong network, which showed breakdown at high deformation (>100% strain). The synergistic strengthening of the network of the mixture was noticeable in the Fourier transform and Chevyshev harmonic analyses. This analysis indicated that the nonlinearity of e3/e1 and v3/v1 started at higher levels of strain for the mixed gels. The FTIR spectra revealed that there was no strong interconnection by crosslinking between pea protein and sodium alginate, indicating that the synergistic effect mainly came from electrostatic interactions. These findings suggest that combining alginate with pea protein can enhance the mechanical properties of gels, making them suitable for various food applications.

Enhanced electrochemical performance of nickel cobalt sulfide microspheres for high energy symmetric supercapacitors

Herein, Nickel cobalt sulfide (NCS) microspheres are successfully synthesized by an easy one-step hydrothermal method at different reaction conditions. The as-synthesized samples are used as electrode material to demonstrate their practical application for supercapacitors (SCs). Various techniques including X-ray diffraction (XRD), Fourier transform infrared spectra (FTIR), Scanning electron microscopy (SEM), Energydispersive X-ray (EDX) spectroscopy are used for structural and morphological characterization of the synthesized materials which confirmed the successful formation of NCS. The electrochemical performance of prepared samples is tested using cyclic voltammetry (CV), galvanostatic charge/discharge (GCD) and electrochemical impedance spectroscopy (EIS). The optimized NCSW-200 sample delivered a remarkable specific capacitance of 369 F g−1 at 0.5 A g−1. The energy and power density exhibited by NCSW-200 sample are as high as 32.8 Wh kg−1 and 266.6 W kg−1, respectively. After 2000 consecutive charge/discharge cycles, capacitance retention of 67% is achieved, depicting better cyclic stability. To illustrate the practical feasibility of the prepared symmetric cells of the optimized sample NCSW-200, a lab scale setup of three SC cells connected in series is fabricated and tested using a red light emitting diode (LED). The SC setup is able to illuminate a red LED for 2.5 minutes. The electrochemical performance demonstrated by NCS microspheres suggests its viable application as supercapacitor electrodes.