FTIR Spectra Research Articles

An efficient synthesis, structural analysis, and computational studies of benzothiazole derivatives activated by formic acid under solvent-free conditions

In the present work, formic acid was used as a low-cost and eco-friendly catalyst to synthesize 2-(2-hydroxyphenyl)benzothiazole (HB) through a cycloaddition process in a solvent-free reaction medium. Imine molecule was synthesized with the help of acetic acid (B). The ring closure and formation of the thiazole moiety give acetic acid distinctiveness as a catalyst. The cyclization of fused HB failed without an acid catalyst. The chemical structures were characterized using microanalysis techniques such as IR, 1H-NMR, and 13C-NMR. The obtained FT-IR spectra were compared to theoretical data using the B3LYP/6-31G* level of theory. The electronic characteristics of molecules can be predicted utilizing wave function-dependent features, such as Average localized ionization energy (ALIE), Localized orbital locator (LOL), Electron localized function (ELF), Reduced density gradient (RDG), and Noncovalent interactions NCI studies, which have provided a wealth of knowledge. The molecular docking study was investigated to explore binding energy and interaction type. Docking analysis displayed binding energies (kcal/mol) of HB with values of -8.29, -6.80, -6.68, -7.43, and -6.69 of acetylcholinesterase (AChE) and butylcholinesterase (BuChE)), SARS-CoV-2 main protease (Mpro), human immunodeficiency virus reverse transcription (HIV RT)) and cytochrome (P450), respectively, which was the most active compound against all receptors. The dramatic improvement of the proposed approach over the existing methods can be used to derive an efficient and successful route for the synthesis of HB. This process provides a fresh and high-yield method for the synthesis of benzimidazoles.

The structural and optical properties of PVA/CMC copolymer cured by UV irradiation for different times

Poly(vinyl alcohol) (PVA)/carboxymethylcellulose (CMC) blend films with equal amounts (0.25 g) of both polymers were prepared through a simple and low-cost comparative casting method. Then, the PVA/CMC blend films were exposed to ultraviolet (UV) radiation for varied time intervals (1, 12, 26, 32, 40 and 48 h). The UV-irradiation effect on the physical properties of as-prepared films, including the structure, morphology, composite and optical properties (transmittance, absorbance and band gap (E g)), was examined. Field-emission scanning electron microscopy images showed that UV irradiation had a strong effect on the shape of PVA/CMC blend films. The X-ray diffraction patterns showed various crystalline qualities in the microstructure of as-synthesized samples. The Fourier transform infrared spectra showed that the UV-irradiation time and CMC film had a positive impact on the blend polymer structure since covalent connections were formed between CMC and PVA. Furthermore, the analysis results of optical inspections showed that the absorbance of the PVA/CMC films improved with an increment in irradiation time from 1 to 40 h. Important tuning of the E g values of blend films was realized. It showed a slight increase from 4.64 to 4.84 eV with increasing irradiation time from 1 to 40 h. The E g value (3.21 eV), however, displayed an inverted behavior due to an increased irradiation time of 48 h. This reduction could be ascribed to the creation of defects inside the blend band gap. Finally, the physical property modification of PVA/CMC blend film using UV irradiation made it an amazing contender in the optoelectronic field.

Synthesis of Green Carbon Dots from Nephelium Lappaceum L. Seeds

In this study, rambutan (Nephelium Lappaceum L.) seeds were used to fabricate green carbon dots (gCDs) by employing a hydrothermal process. The synthesized CDs were evaluated using Fourier transform infrared (FT-IR) and X-ray photoelectron spectroscopy (XPS) for the structural properties as well as UV-Vis and fluorescence spectrophotometry for the optical properties. UV-Vis examination revealed that the produced gCDs showed emission-dependent photoluminescence excitation, with two absorption peaks at 265 nm and 330 nm. The presence of functional groups and chemical composition such as C=C, C=O, -COOH, and -OH on the surface of gCDs was confirmed by the results of FTIR and XPS spectra. Consequently, gCDs present several opportunities for exploration in a range of applications.

Carboxylic acid modulated in situ growth of Zr-based MOFs on carboxylated cotton fabrics for removal of Cr(VI) from aqueous solutions

In this paper, carboxylated cotton fabric (CF-Ph-COOH) were obtained as active substrate by diazonium radical polymerization modification of cotton fibers. Then the MOF fabric composites were prepared by in situ growth of metal zirconium ions (Zr) and organic ligands on the surface of carboxylated cotton fabrics under carboxylic acid modifier. MOF fabric composites with controllable morphologies structures were achieved by regulating organic ligands, reaction time the type and dosage of regulator (formic acid and acetic acid). The prepared acetic acid regulated MOF fabric composites were designated as CF-HAc1-UiO-66, CF-HAc2-UiO-66, CF-HAc1-UiO-66-NH2, and CF-HAc2-UiO-66-NH2, respectively, and the formic acid regulated as CF-FA-UiO-66 and CF-FA-UiO-66-NH2. The fabricated carboxylic acid modulated MOF fabric composites were well characterized using SEM, TGA, XRD, FTIR, and XPS spectra. The adsorption experiment results show that carboxylic acid modulated Zr based MOF fabric composites can serve as adsorbent for effective removal of Cr(VI) from water, in which the CF-FA-UiO-66-NH2 was prepared under the ratio of ZrCl4 and BDC-NH2 is 1.006 and with 5.47 M formic acid regulator exhibits that the optimal adsorption efficiency and the removal efficiency is 79.5 %. In addition, the adsorption of Cr(VI) in water by CFA-UiO-66-NH2 showed a quasi-secondary kinetic model following the Langmuir adsorption model, showing a a typical of chemisorption. What’s more, the Cr(VI) removal efficiency and saturated adsorption capacity of CF-FA-UiO-66-NH2 was up to 80 % and 318.85 mg/g, respectively. The prepared CF-FA-UiO-66-NH2 MOF fabric composite was recyclable for removal of Cr(VI), and could be used as the potential adsorbent membrane for waste water treatment.

Green Synthesis of Iron Nanoparticles Using an Aqueous Extract of Strawberry (Fragaria × ananassa Duchesne) Leaf Waste

In this study, we analysed the potential use of dried strawberry leaves and calyces for the production of nanoparticles using inorganic iron compounds. We used the following iron precursors FeCl3 × 6H2O, FeCl2 × 4H2O, Fe(NO3)3 × 9H2O, Fe2(SO4)3 × H2O, FeSO4 × 7H2O, FeCl3 anhydrous. It was discovered that the content of polyphenols and flavonoids in dried strawberries and their antioxidant activity in DPPH and FRAP were 346.81 µM TE/1 g and 331.71 µM TE/1 g, respectively, and were similar to these of green tea extracts. Microimages made using TEM techniques allowed for the isolation of a few nanoparticles with dimensions ranging from tens of nanometres to several micrometres. The value of the electrokinetic potential in all samples was negative and ranged from −21,300 mV to −11,183 mV. XRF analyses confirmed the presence of iron ranging from 0.13% to 0.92% in the samples with a concentration of 0.01 mol/dm3. FT-IR spectra analyses showed bands characteristic of nanoparticles. In calorimetric measurements, no increase in temperature was observed in any of the tests during exposure to the electromagnetic field. In summary, using the extract from dried strawberry leaves and calyxes as a reagent, we can obtain iron nanoparticles with sizes dependent on the concentration of the precursor.

Utilization of Natural Adsorbents in the Purification of Used Sunflower and Palm Cooking Oils

The purification of used oils and their introduction into production cycles lead to reduction in environmental contamination. A simulation was conducted to study the thermal degradation of sunflower oil under varying temperatures over time. In the purification process of used cooking oil, an adsorption technique using zeolite and eggshell as an adsorbent (5, 10, 20, and 30 g/100 mL used oil) was applied. To optimize purification, different doses of thermally and chemically activated adsorbents were used, at different temperatures (30 and 80 °C). Therefore, this study was conducted in batch operations to determine the effect of suitable adsorption for a contact time of the adsorbent of 2 h. In comparison, the purification of used vegetable oils was achieved using a saline solution. The adsorption capacity was evaluated by determining the physicochemical parameters of the oils before and after purification. The characterization of natural adsorbents was carried out using scanning electron microscopy (SEM) and X-ray fluorescence spectrometry (XRF). The results showed that the adsorbent in a dose of 30 g of zeolite activated with NaOH and heat-treated eggshell, respectively, exhibited a larger surface area and greater adsorption capacity. Adsorption increased with contact time. The FT-IR spectra of the oils showed the IR bands at 1097, 1160, and 1237, corresponding to the presence of the ester C-O-, 1743 for C=O ester, 2853, 2922 for (CH2, CH3), and 3008 for (C=C). The acidity and peroxide values decreased with increasing dose and contact time with zeolite or eggshell. Together, our result strongly suggests that natural adsorbents contribute to the purification of used oils.

Static Compaction on Coupled Precursors and Optimizing Molarity for Enhanced Strength and Durability of Geopolymer

The static compaction technique emphasizes the reduced activator dosage required to develop geopolymers. Therefore, it is crucial to comprehend the optimal alkaline activator concentration for blending low-calcium precursor (fly ash) with high-calcium precursor (GGBS) to produce geopolymer blocks. This work was designed to optimize structural blocks’ compressive strength and durability. In experimentation, fly ash (FA) and slag (GGBS) proportions were initially investigated under NaOH solution with varying molarity (8–12) and curing conditions to develop a load-bearing structural block. Subsequently, the durability of the optimized block was evaluated over 56 days through subjection to sulfate and acidic solutions, with efflorescence monitored over the same period. The results reveal that the structural block comprised of 100% FA exhibits the highest compressive strength and lowest bulk density. Conversely, the block incorporating 25% slag that underwent hot curing demonstrates a remarkable 305% strength increase compared to ambient curing. Considering the physico-mechanical performance, the 100% FA block was chosen for durability investigation. The findings indicate a substantial strength loss exceeding 40% after exposure to sulfate and acidic environments over 56 days, coupled with pronounced efflorescence. Catastrophic failure occurs in all cases due to significant strength deterioration. The FTIR spectrum revealed the shifting of the wavenumber to a higher value and verified the depolymerization and leaching of alumina under acidic exposure. However, the developed geopolymer blocks demonstrate superior sustainability and feasibility compared to conventional fired clay bricks and cement-based FA bricks. Despite slightly higher costs, these blocks exhibit greater strength than their counterparts after enduring severe exposures.

Physical and biological study of Lanthanum trioxide/samarium trioxide/graphene oxide/chitosan-based films for Wound healing purpose

Investigations are being conducted on chitosan-based polymeric films that have been encapsulated with lanthanum, samarium, and graphene oxide. The primary distinguishing signals of chitosan (CS) and other components were seen in the FTIR spectra. Additionally, the interaction of the CS with the oxy-components clearly increased the crystallinity, as shown by the XRD pattern. The optical data shows that both Sm2O3 and GO cause diminishing in band gap while lanthanum oxide cause a significant widening in it. Additionally, this study discusses the impact of mixed oxides insertion on the cytotoxicity of La2O3/Sm2O3/GO@CS film toward human lung cell-line. Cell viability is seen to be 123.21 % when 2.2 g/ml is utilized, and 117.95 % when 4.4 g/ml is used. Viability percentages of 29.49 and 27.31 % are obtained using 2250 and 4500 g/ml, respectively. The obtained data showed that the CS-based films behaved in a promising way when it came to healing wounds.

Effect of Sodium Laureth Sulfate on Contact Angles of High-Impact Polystyrene and Acrylonitrile–Butadiene–Styrene from Recycled Refrigeration Equipment

This paper investigates the effects of sodium laureth sulfate (SLES) on the wettability of the surface of the two most common recycled plastics in refrigeration equipment: HIPS (high-impact polystyrene) and ABS (acrylonitrile–butadiene–styrene). These plastics, in the form of flakes, were identified on the basis of their FTIR spectra, and then, they were subjected to a study of contact angles using the sessile droplet method. The solutions for the angle analysis included tap water with the addition of SLES. The results of this study showed that at SLES concentrations of 0.1 g/L and 0.2 g/L, the differences in the contact angles for HIPS and ABS were 10.76° and 10.10°, respectively. This research confirmed the potential of using SLES as a support for the flotation separation of plastics with similar densities and surface characteristics, such as HIPS and ABS.

Investigation of the Degree of Monomer Conversion in Dental Composites through Various Methods: An In Vitro Study

The degree of monomer conversion (DC) values of three different dental composites were examined using three different methods: surface microhardness (ratio of bottom/top), Fourier-transform infrared (FT-IR), and differential scanning calorimetry (DSC). Two of the dental composites included in the study were nanohybrid (Dentsply Neo Spectra ST HV and Omnichroma), and one was a microhybrid-labeled newly marketed composite containing nanoparticles (Dentac Myra). Composite discs were prepared according to the methodology for all methods and analyzed (2 mm thickness × 5 mm diameter). Surface microhardness values were measured in Vickers Hardness Number (VHN), while FT-IR and DSC values were obtained in percentage (%). Significant differences were observed in both bottom/top surface microhardness values and DC values obtained from FT-IR. However, there was no statistical difference in the ratio of bottom/top microhardness values. Neo Spectra ST HV exhibited superior performance in both microhardness and monomer conversion compared to the other two composites. Newly marketed Myra showed values close to Omnichroma. It was found that the values obtained by the DSC method were parallel to those obtained by FT-IR. In conclusion, the structure of dental composites leads to different mechanical properties. Additionally, DSC measurements and FTIR spectra were found to be complementary techniques for characterizing monomer conversion values.

Metal-organic decomposed lanthanum cerium oxide thin films: A study of chemical and surface properties

Lanthanum cerium oxide thin films have been deposited on n-type (100) silicon wafers using the spin coating technique. The post-deposition annealing was performed over spin-coated films. The compositional studies were conducted by performing Fourier transform infrared spectroscopy, Energy dispersive X-ray spectroscopy, and X-ray diffraction. Ellipsometry was used to determine the thickness and atomic force microscopy was performed to understand the surface morphology of the deposited thin films. The effect of rapid thermal annealing at different temperatures over the structural and chemical properties of the LaCeO2 thin films was observed. The FTIR spectra show the formation of silicates at the interface of the oxide and semiconductor, while XRD results show that the films become crystalline with increased annealing temperature. The refractive index was observed to be reduced with an increase in the annealing temperature and a minor reduction in the physical thickness as per the sample standard deviation of 0.2981[Formula: see text]nm.

Dystrophic calcinosis: structural and morphological composition, and evaluation of ethylenediaminetetraacetic acid (‘EDTA’) for potential local treatment

BackgroundTo perform a detailed morphological analysis of the inorganic portion of two different clinical presentations of calcium-based deposits retrieved from subjects with SSc and identify a chemical dissolution of these deposits suitable for clinical use.MethodsChemical analysis using Fourier Transform IR spectroscopy (‘FTIR’), Raman microscopy, Powder X-Ray Diffraction (‘PXRD’), and Transmission Electron Microscopy (‘TEM’) was undertaken of two distinct types of calcinosis deposits: paste and stone. Calcinosis sample titration with ethylenediaminetetraacetic acid (‘EDTA’) assessed the concentration at which the EDTA dissolved the calcinosis deposits in vitro.ResultsFTIR spectra of the samples displayed peaks characteristic of hydroxyapatite, where signals attributable to the phosphate and carbonate ions were all identified. Polymorph characterization using Raman spectra were identical to a hydroxyapatite reference while the PXRD and electron diffraction patterns conclusively identified the mineral present as hydroxyapatite. TEM analysis showed differences of morphology between the samples. Rounded particles from stone samples were up to a few micron in size, while needle-like crystals from paste samples reached up to 0.5 µm in length.Calcium phosphate deposits were effectively dissolved with 3% aqueous solutions of EDTA, in vitro. Complete dissolution of both types of deposit was achieved in approximately 30 min using a molar ratio of EDTA/HAp of ≈ 300.ConclusionsStone and paste calcium-based deposits both comprise hydroxyapatite, but the constituent crystals vary in size and morphology. Hydroxyapatite is the only crystalline polymorph present in the SSc-related calcinosis deposits. Hydroxyapatite can be dissolved in vitro using a dosage of EDTA considered safe for clinical application. Further research is required to establish the optimal medium to develop the medical product, determine the protocol for clinical application, and to assess the effectiveness of EDTA for local treatment of dystrophic calcinosis.

Investigating the Functional Performance of Plantago Ovate Plant as a Drug Carrier in a Targeted Drug Delivery System

The drug delivery systems that were used in the past were done without any control over the time, place and speed of drug release, and this caused the amount of drug released in the blood to fluctuate, that is, the concentration of the drug in the blood could vary from The therapeutic range will be exceeded and its side effects will also increase. Therefore, with targeted medicine, it is possible to control the place of drug release, its speed and time, and minimize the side effects caused by the drug. In this regard, in this research, the natural hydrogel extracted from the Plantago ovate plant as one of the drug carriers in the body environment in order to increase the efficiency and reduce the degradation of the drug, prevent the side effects caused by the use of the drug and increase the access to the drug and improve Its effect was investigated at the lesion site. In this context, after extracting the natural hydrogel from Plantago ovate plant, the swelling rate of Plantago ovate gel powder was investigated at different pH, the FT-IR spectrum obtained from Plantago ovate hydrogel and the swelling rate of Plantago ovate mucilage at different pH were investigated. Therefore, the obtained results indicate that natural polysaccharides can be used as a natural drug carrier in drug delivery systems due to their high biocompatibility in the body environment, non-toxicity and cheapness.

Characterization of Polyphenol Composition and Starch and Protein Structure in Brown Rice Flour, Black Rice Flour and Their Mixtures

The study investigates the structural and chemical properties of brown rice flour (WRF), black rice flour (BRF) and their mixtures in ratios of 25%, 50% and 75% to provide reference information for the gluten-free bakery industry. BRF contains higher concentrations of proteins, lipids, total minerals, crude fiber, total polyphenols, proanthocyanidins and flavonoids than WRF. A higher amylose content in BRF than in WRF resulted in flour mixtures with slower starch digestion and a lower glycemic response depending on the BRF ratio added. Differences in the chemical composition of WRF and BRF led to improved composition of the flour mixtures depending on the BRF ratio. The presence of anthocyanidins and phenolic acids in higher concentrations in the BRF resulted in a red–blue color shift within the flour mixtures. The deconvoluted FTIR spectra showed a higher proportion of α-helixes in the amide I band of BRF proteins, indicating their tighter folding. An analysis of the FTIR spectra revealed a more compact starch structure in BRF than in WRF. By processing reflection spectra, nine optically active compound groups were distinguished in rice flour, the proportion in BRF being 83.02% higher than in WRF. Due to co-pigmentation, the bathochromic shift to higher wavelengths was expressed by the proanthocyanins and phenolic acids associated with the wavelengths 380 nm to 590 nm and at 695 nm. Anthocyanins, protein–tannin complexes, methylated anthocyanins and acylated anthocyanins, associated with wavelengths 619, 644 and 668 nm, exhibited a hypsochromic effect by shifting the wavelengths to lower values. This research represents a first step in the development of rice-based products with increased nutritional value and a lower glycemic index.

Simultaneous Removal of Setazol Navy Blue and Cr(VI) By Mixed Microbial Culture Isolated from the Çubuk Stream

Water samples taken from the Çubuk Stream (Ankara, Turkey) were inoculated into nutrient broth media containing Setazol Navy Blue SBG (SNB), an organic pollutant, and heavy metal Cr(VI), an inorganic pollutant, to obtain a pollutant-resistant mixed microbial culture. Experiments were conducted with this culture to remove SNB and heavy metal. The optimum conditions, where the mixed bacterial culture removed the pollutants most effectively, were determined, showing that the highest capacity for removal took place at pH 8 with removal percentages 96.3% for Cr(VI) and 78.5% for SNB. In media with 50.4 mg/L SNB and 9.7 mg/L Cr(VI), the SNB removal was 87.3%, and the Cr(VI) removal was 96.6% at the end of the 7-day incubation period. The highest removal was observed with a biomass concentration of 8% (v/v) of mixed culture [50 mg/L SNB dye+25 mg/L Cr(VI)]. The removal was 100% for both Cr(VI) and the SNB dye. The bacteria with the highest removal were isolated and identified using 16S rDNA gene sequence analysis as Microbacterium oxydans and Leucobacter aridicollis. The role of various functional groups and the structures of the microorganisms that might be involved in the removal mechanisms were discussed using their FTIR spectra. This report is the first study that investigates a mixed bacterial culture and pure cultures (M. oxydans and L. aridicollis) isolated from that mixed culture, removing both SNB and Cr(VI) simultaneously.

Multiple comonomer concentrations prediction from FTIR spectra with quantum chemistry-based interpretation

Multiple comonomer concentrations prediction from FTIR spectra with quantum chemistry-based interpretation

Synthesis of Green Brucite [NixMg1−x(OH)2] by Incorporation of Nickel Ions in the Periclase Phase (MgO) Applied as Pigments

Magnesium oxide is typically white and can be colorized with transition metal insertion by doping. We present the preparation of a green-colored hydroxide by the exchange of Mg2+ on the crystalline lattice with Ni2+ in MgO, using three nickel salts. MgOst was prepared by the colloidal starch suspension method, using cassava starch. The oxides and hydroxides, before and after, were characterized by X-ray diffraction (XRD), and show that a phase change occurs: a transition from periclase (MgO) to brucite (Mg(OH)2) due to the incorporation of nickel ions from different salts (acetate, chloride, and nitrate), resulting in the solid solution [NixMg1−x(OH)2]. The FTIR spectrum corroborates the crystallographic structure identified through XRD patterns, confirming the formation of a crystal structure resembling brucite. The new samples present a green color, indicative of the incorporation of the Ni2+ ions. The antimicrobial activity of products resulting from the doping of magnesium oxide with nickel and the precursor MgOst was assessed through the minimum inhibitory concentration (MIC) test. The evaluation included three bacterial strains: Staphylococcus aureus (ATCC 25923), Escherichia coli (ATCC 25922), Salmonella gallinarum (ATCC 9184), and a yeast strain, Candida albicans (ATCC 10231). The obtained results were promising; the tested samples exhibited antimicrobial activity, with a MIC ranging from 0.312 to 0.625 μg.μL−1. The nickel compound, derived from the precursor chloride salt, demonstrated superior MIC activity. Notably, all tested samples displayed bactericidal activity against the S. aureus strain and exhibited a broad spectrum of inhibition, encompassing both Gram-positive and Gram-negative strains. Only the nickel compounds derived from precursors with acetate and nitrate anions demonstrated antimicrobial activity against C. albicans, exhibiting a fungistatic behavior. Based on the conducted studies, [NixMg1−x(OH)2] has emerged as a promising antimicrobial agent, suitable for applications requiring the delay or inhibition of bacterial growth.

Zeolite Synthesis Based Silica from Saccharum officinarum L. with Black Stem Using the Hydrothermal Method

Saccharum officinarum L. has a high amount of silica content, which can be used as the main component of zeolite synthesis. Silica was isolated from Saccharum officinarum L. bagasse with NaOH and HCl. This research aims to synthesize zeolite using silica from Saccharum officinarum L. with black stem and alumina from aluminium foil. The Saccharum officinarum L. used in this research was sourced from Lombok Island, West Nusa Tenggara Province, Indonesia. Silica was sourced from Saccharum officinarum L. using the sol-gel method. The silica from the isolation of dregs ash obtained 20 g of silica with a high percentage (yield) of 50%. This study found that 5.29 g of aluminium foil produced 14.29 g of alumina with the addition of 22.50 g of Na2CO3. The zeolite obtained was 3.88 g with a SiO2:Al2O3 ratio of 5:3. From this study, the percent (%) of obtained zeolite was 48.5% from the weight of the silica and alumina produced. The zeolite results synthesized from Saccharum officinarum L. ash were characterized using FTIR. Based on the FTIR results, absorption was found at wave numbers (cm-1) 960, 729, and 668. The zeolite obtained was pure white and had a FTIR spectrum similar to that of Zeolite X from previous research. It can be predicted that the zeolite obtained from this research has been formed. This research is expected to be useful in increasing the effectiveness of the silica extraction process from Saccharum officinarum L. with black stem. Further analysis using XRD and SEM is needed to determine the characteristics of the zeolite produced.

Extraction of Pithecellobium clypearia Benth polysaccharides by dual-frequency ultrasound-assisted extraction: Structural characterization, antioxidant, hypoglycemic and anti-hyperlipidemic activities

In this research, the extraction process of polysaccharides from Pithecellobium clypearia Benth (PCBPs) was optimized using dual-frequency ultrasound-assisted extraction (DUAE). The biological activities of PCBPs were investigated by in vitro antioxidant, hypoglycemic, and anti-hyperlipidemic assay. High-performance anion-exchange chromatography, high-performance gel permeation chromatography, SEM, UV–Vis spectroscopy, and FT-IR spectra were used to analyze the monosaccharide composition, molecular weight, microscopic morphology, and characteristic structure of PCBPs. The results showed that the maximum extraction rate of PCBPs was 9.90 ± 0.16% when the ultrasonic time was 8 min, the liquid-to-material ratio was 32 mL/g, and the ultrasonic power was 510 W. The PCBPs also possessed excellent in vitro antioxidant, hypoglycemic, and anti-hyperlipidemic activities. In addition, the average molecular weight of PCBPs was 15.07 kDa. PCBPs consisted of rhamnose, arabinose, galactose, glucose, xylose, mannose, and glucuronic acid, with the molar ratios of 11.07%, 18.54%, 48.17%, 10.44%, 4.62%, 4.96%, and 2.20%, respectively. Moreover, the results of SEM showed that PCBPs mainly showed a fine spherical mesh structure. The above studies provided a valuable theoretical basis for the subsequent in-depth study of PCBPs.

Synthesis and characterization of iron oxide nanoparticles from Lawsonia inermis and its effect on the biodegradation of crude oil hydrocarbon.

Crude oil hydrocarbons are considered major environmental pollutants and pose a significant threat to the environment and humans due to having severe carcinogenic and mutagenic effects. Bioremediation is one of the practical and promising technology that can be applied to treat the hydrocarbon-polluted environment. In this present study, rhamnolipid biosurfactant (BS) produced by Pseudomonas aeruginosa PP4 and green synthesized iron nanoparticles (G-FeNPs) from Lawsonia inermis was used to evaluate the biodegradation efficiency (BE) of crude oil. The surface analysis of G-FeNPs was carried out by using FESEM and HRTEM to confirm the size and shape. Further, the average size of the G-FeNPs was observed around 10nm by HRTEM analysis. The XRD and Raman spectra strongly confirm the presence of iron nanoparticles with their respective peaks. The BE (%) of mixed degradation system-V (PP4+BS+G-FeNPs) was obtained about 82%. FTIR spectrum confirms the presence of major functional constituents (C=O, -CH3, C-O, and OH) in the residual oil content. Overall, this study illustrates that integrated nano-based bioremediation could be an efficient approach for hydrocarbon-polluted environments. This study is the first attempt to evaluate the G-FeNPs with rhamnolipid biosurfactant on the biodegradation of crude oil.