Retention Factors Research Articles

Focusing on the corrosion resistance enhancement of HRB400 rebar by Cr addition in the marine envrionment

The corrosion resistance of Cr reinforced HRB400 rebar in the marine environment was investigated. The addition of Cr increases the amount of Cr(OH)3 and α-FeOOH in the passivate film, resulting in a denser passivate film structure. This enhanced passivation film inhibits localized corrosion. The pitting potential and critical chloride concentration (CTL) of the steel increased with the increase in chromium content, indicating improved corrosion resistance of the steel. On the other hand, an increase in the concentration of Cl- in solution leads to a decrease in the pitting potential and resistance of the steel, which reduces the corrosion resistance. At higher Cl- concentrations, the Cl- ions form an electrochemical interface with the steel surface, resulting in a sharp decrease in the Rf value. In addition, the gradual decrease in solution pH leads to a decrease in the pitting potential and CTL of HRB400 and 1.5Cr steel. The corrosion resistance was also found to be reduced, pH reduction accelerated the intrusion of chloride ions, which led to a severe breakdown of the passivation film.

Estimation of Effective Fracture Aperture in Glacial Tills by Analysis of Dye Tracer Penetration.

This study advances a methodology to estimate effective apertures of fractures in glacial tills based on dye tracer infiltration tests and numerical simulations. The approach uses the visible penetration depth of the dye tracer along fracture flow paths as primary information to calculate effective fracture apertures. Further data used in the calculation are the dye tracer input concentration and retardation, the duration of the tracer injection, and the hydraulic gradient applied to control the infiltrating water fluxes. The method does not require measurement of hydraulic conductivity for the fractured till and enables direct observation of flow and transport patterns within the fractures (e.g., uniform flow and dye tracer distribution, channeling due to aperture variability, and presence of biogenic macropores in fractures). The approach was successfully verified by using the estimated effective fracture aperture values in Large Undisturbed Columns (LUCs) to consistently simulate both the observed LUC effluent breakthrough of a conservative bromide tracer and the water fluxes with the hydraulic gradient applied in the experiments. Sensitivity analyses revealed that estimation of small effective fracture apertures (<10 μm) required accurate determination of the dye tracer retardation factor. By contrast, in the case of larger effective apertures (>20 μm), the sensitivity of the estimated effective fracture aperture to variations in the porous material and solute transport parameters was low compared to the dominant sensitivity to the water flow through the fractures (cubic relation between flow and aperture). The proposed approach may be extended beyond laboratory applications and assist in characterizing field-scale fracture networks.

Development and optimization of high-performance extraction chromatography method for separation of rare earth elements

The effectiveness of commonly used extractants for chromatographic separation of rare earth elements (REEs) was compared. Columns loaded with similar molar concentrations of tributyl phosphate (TBP), di-(2-ethylhexyl) phosphoric acid (HDEHP), and N-Methyl-N, N, N-tri-octyl-ammonium chloride (Aliquat-336), with mineral acid as eluent were evaluated. Retention factors were determined, and separation efficiency was assessed based on the resolution data of the REEs acquired under the same elution conditions for each column. HDEHP demonstrated the best separation efficiency for the entire REE series (mean Rs = 2.76), followed by TBP (mean Rs = 1.52), while Aliquat-336 exhibited the lowest performance (mean Rs = 1.42). The HDEHP-coated column was then used to optimize the extraction chromatographic separation of the REEs. The primary challenge was to completely elute the heavy REEs (Tb – Lu) while maintaining adequate separation of the light REEs (La – Gd) within a reasonably short time. The stepwise gradient elution procedure improved the resolution between adjacent REEs, allowing the complete separation of the entire REE series within 25 minutes. Better separation efficiency for light REEs was achieved at higher column temperatures and a mobile phase flow rate of 1.5 mL/min in the tested domain of 20–60 °C, and 0.5–2.0 mL/min, respectively, resulting in plate heights (H) ranging from 0.011 to 0.027 mm.

Comparative study of UV spectroscopy, RP-HPLC and HPTLC methods for quantification of antiviral drug lamivudine in tablet formulation

BackgroundIn the current study, estimation of lamivudine (LMU) by UV spectroscopy, reverse-phase HPLC (RP-HPLC) and HPTLC methods in tablet formulation was developed, and comparative studies between the methods were investigated by analytical results and statistical test analysis of variance (ANOVA) to find out best method. In the UV spectral method, LMU was quantified at 271 nm absorption maxima using methanol as the solvent. In the RP-HPLC method, the Shimadzu C18 column (250 mm × 4.6 mm i.d., 5 µm particle size) was employed for chromatographic separation. The mobile phase used consists of methanol: water (70:30 v/v) in an isocratic mode with a 1.0 mL/min flow rate. In the HPTLC method, the chromatogram was developed on a pre-coated plate of silica gel 60 F254 with a mobile phase composition of chloroform: methanol (8:2 v/v). The quantification was performed at an absorbance mode of 271 nm by densitometry. The methods were validated according to the International Conference on Harmonization (ICH) guideline Q2 (R1). The degradation conditions were employed as per ICH guidelines Q1A(R2) and Q1B which include acid, alkaline, neutral, thermal and photostability to determine the intrinsic stability of the drug in varied environmental conditions.ResultsLMU absorption maxima was found to be 271 nm. The retention time of LMU was 3.125 min, and the total analysis time was 5 min. The Rf value of LMU was 0.49–0.62. The methods were linear within 2–12 μg/mL range. The correlation coefficient (r2) for UV, HPLC and HPTLC was 0.9980, 0.9993 and 0.9988, and percent recoveries were calculated as 98.40–100.52%, 99.27–101.18% and 98.01–100.30%, respectively, with percentage relative standard deviation (RSD) less than 2% showing that methods were precise and accurate.ConclusionDeveloped UV, RP-HPLC and HPTLC methods are free from intervention caused by excipients present in tablets and thus can be used for regular quantitative analysis of LMU in tablet formulation. Based on analytical results and statistical tests, ANOVA, it is inferred that the HPLC method is best for LMU quantification tablet formulation due to its high reproducibility, good retention time and sensitivity; it has a higher percent recovery and has less analysis time, i.e., 5 min. The degradation peaks were well separated from the LMU peak indicating stability of the HPLC method.

A logarithmic law for the velocity- and retention-dependency of the eddy dispersion in chromatographic columns

Applying the recently introduced patchwork model for porous media, we present a new step forward in the modelling of eddy dispersion in chromatographic columns. The logarithmic law describing the velocity dependency emerging from this patchwork model is supplemented with a retention factor dependency via first principles modelling of the variations in flow resistance and retention capacity caused by the packing disorder. Furthermore, it is shown the derived expression is also able to fit the eddy dispersion originating from the wall effect on the packing. When applied to literature data of eddy dispersion, the newly introduced logarithmic law has a goodness of fit that is at least equal to that of Knox’ empirical power law (R2>0.98). The main difference is that, whereas Knox’ power law requires a separate fit for each component due to the retention factor dependency, the present model simultaneously fits all plate height curves measured on one chromatographic column, using only two parameters with a clear physical meaning.

Proper retention factor for Avanafil and Dapoxetine Hydrochloride Separation and Validation with RP-HPLC in Bulk, Dosage Form and Rat Plasma; Validation, Degradation, and Pharmacokinetic Application

Proper retention factor for Avanafil and Dapoxetine Hydrochloride Separation and Validation with RP-HPLC in Bulk, Dosage Form and Rat Plasma; Validation, Degradation, and Pharmacokinetic Application

The Effect of Different Ethanol Concentrations as The Extraction Solvent on Total Flavonoid Content of White Mulberry Leaves Extracts (Morus alba L.)

White mulberry leaves (Morus alba L.) contain flavonoid which empirically have many health benefits, such as reducing fever, relieving headaches and throats, coughs, dysentery, digestive disorders, flu, and according to research it has antioxidant activity. Many factors effect the total flavonoid content, one of which is the concentration of the extraction solvent. The purpose of the research was to determine the effect of different ethanol concentrations as the extraction solvent on total flavonoid content of white mulberry (Morus alba L.) leaves extract. White mulberry leaves (Morus alba L.) were extracted using the maceration method, the extract was tested for phytochemical screening and thin layer chromatography using chloroform: ethyl acetate (6: 4) as the eluent. The resulting spots were observed visually and with λ 254 nm and λ 366 nm UV light. Determination of flavonoid content by UV-Vis spectrophotometry using the AlCl3 colorimetric method at a maximum wavelength of 415 nm. The research results showed that the yield of 50% and 96% ethanol extract of white mulberry leaves (Morus alba L.) was 17.42 % and 11.04 %. Phytochemical screening showed that both extracts positively contained flavonoids. The presence of flavonoids was confirmed using a thin layer chromatography test, resulting in an average Rf value for 50% and 96% ethanol extracts are 0.71 and 0.70, close to quercetin Rf standard is 0,73 as comparison. The total flavonoid content obtained from the 50% ethanol extract was 36.0902 mgQE/g and the 96% ethanol extract was 56.4699 mgQE/g. The conclusions are the concentration of the extraction solvent effect the yield and total flavonoid content.

Risk factors for postoperative urinary retention in fragility hip fracture patients: a prospective study

BackgroundPostoperative urinary retention (POUR) among older patients with hip fractures is common and may result in delayed ambulation, prolonged hospital stays, and urinary tract infections. Although preoperative urinary catheter indwelling and early postoperative removal can prevent perioperative urinary retention, this condition may occur in some patients after catheter removal, which requires urinary catheter re-indwelling or intermittent catheterization. Therefore, this study aims to identify risk factors and develop a screening tool for postoperative urinary retention in patients who have undergone operative treatment for fragility hip fractures subsequent to urinary catheter removal.MethodsA prospective cohort study of 145 fragility hip fracture in older patients who were operatively treated between September 2020 and May 2022 was conducted. All patients were evaluated for urine retention after urinary catheter removal using a bladder scan. In addition, factors related to urinary retention were collected and utilized for screening tool development.ResultsOf the included patients, 22 (15.2%) were diagnosed with POUR. A multivariable logistic regression model using a stepwise backward elimination algorithm identified the current use of drugs with anticholinergic effect (OR = 11.9, p = 0.012), international prostate symptom score (IPSS) ≥ 8 (OR = 9.3, p < 0.001), and inability to independently get out of bed within 24 h postoperatively (OR = 6.5, p = 0.051) as risk factors of POUR. The screening tool that has been developed revealed an excellent performance (AuROC = 0.85, 95%CI 0.75 to 0.91) with good calibration and minimal optimism.ConclusionsCurrent use of drugs with anticholinergic effects, IPSS ≥ 8, and inability to independently get out of bed within 24 h postoperatively are significant variables of POUR. For additional external validation, a proposed scoring system for POUR screening was developed.Trial registrationThe study protocol was retrospectively registered in The Thai Clinical Trials Registry (TCTR20220502001: 2 May 2022).

Extraction and Purification of Squalene from Virgin Olive Oil via Catalytic Transesterification and Molecular Distillation

Squalene, a highly valuable compound abundant in various natural sources, shows great potential in pharmaceutical, cosmetic, and nutraceutical applications. This research article outlines a comprehensive methodology for extracting and purifying squalene from virgin olive oil, a rich source of the compound. The extraction process begins with degumming, which involves heating the olive oil to 60-70°C to reduce viscosity, followed by the addition of 2-3% warm water to hydrate phospholipids. Food-grade phosphoric acid is then added to react with the phospholipids, forming precipitates. The mixture is stirred for 20-30 minutes and allowed to rest for an additional 20-30 minutes, enabling impurities to settle. The upper layer of degummed oil is separated via decantation or centrifugation and washed with warm water for pH adjustment. Next, transesterification is performed by mixing 100 ml of virgin olive oil with 25% methanol (w/w) and a catalyst (0.5% sodium methoxide or PTSA), and heating the mixture to 80-90°C under reflux for 1-2 hours. Following transesterification, the solvent and acetone are distilled out, and acetone precipitation is repeated 2-3 times to remove unsaponified matter, which is then filtered and evaporated. The concentrated oil undergoes molecular distillation at 180°C and 0.0033 bar pressure for 1 hour, yielding the distillate and residue for further analysis. Qualitative analysis using Thin Layer Chromatography (TLC) involves Merck TLC plates with silica gel 60 F254 and a hexane: chloroform (9:1) mobile phase. Spots are developed with a 10% HCl solution, confirming the presence of squalene with an RF value of 0.93. Quantitative analysis via High-Performance Thin-Layer Chromatography (HPTLC) employs Merck TLC plates with cyclohexane as the mobile phase and CAMAG at 254 nm and 366 nm wavelengths, revealing a squalene purity of 67% and a recovery rate of 69.8%. The initial purification through transesterification facilitated the conversion of ester groups, yielding squalene-rich fractions, while acetone precipitation effectively removed saponified matter. Molecular distillation further enhanced squalene purity. TLC analysis confirmed the qualitative presence of squalene, and HPTLC provided precise quantitative measurements. The obtained squalene purity of 67% significantly enriches the initial content in virgin olive oil, though further optimization could enhance purity and yield. Complementary techniques like GC-MS or HPLC could validate the purification process. This study presents an efficient, replicable procedure for extracting and purifying squalene from virgin olive oil, with significant implications for pharmaceutical, cosmetic, and nutraceutical industries. The findings support a sustainable and ethical shift towards vegetable-derived squalene, meeting market demands while ensuring high-quality production.

Preparation of carboxyl-functionalized silica core-shell microspheres and their applications in weak cation exchange chromatography, heavy metal removal, and lysozyme enrichment.

Chromatography is a technique of separation based on adsorption and/or interaction of target molecules with stationary phases. Herein, we report the design and fabrication of BTDA@SiO2 core-shell microspheres as a new class of stationary phase and demonstrate its impressive performance for chromatographic separations. The silica microspheres of BTDA@SiO2 were synthesized by in situ method with 1,3,5-benzenetricarboxaldehyde and 3,5-diaminobenzoic to separate peptides and proteins on high-performance liquid chromatography. The BTDA@SiO2 core-shell structure has a high specific surface area and retention factor of 4.27 and 8.31 for anionic and cationic peptides, respectively. The separation factor and resolution were high as well. A typical chromatogram illustrated nearly baseline resolution of the two peptides in less than 3 min. The BTDA@SiO2 was also highly stable in the pH range of 1 to 14. Furthermore, the prepared BTDA@SiO2 core-shell material not only be used for chromatographic separation but also as heavy metal removal from water. Using a BTDA@SiO2, we also achieved a lysozyme enrichment with a maximum saturated adsorption capacity reaching 714mg/g. In summary, BTDA@SiO2 has great application prospects and significance in separation and purification systems.

Retention mechanisms of dipeptides on superficially porous particle vancomycin- and teicoplanin-based chiral stationary phases

Retention mechanisms of dipeptides on superficially porous particle vancomycin- and teicoplanin-based chiral stationary phases

Comprehensive in vitro evaluation of Indigofera hochstetteri Baker extract: Effect of chemicals in antimicrobial, anticancer, anti-inflammatory, and anti-diabetic activities

The study aimed to analyze the pharmacological properties of medicinal plant Indigofera hochstetteri Baker extracts. Preliminary phytochemical analysis revealed a diverse range of secondary metabolites present in it. TLC analysis detected numerous phytochemicals with varying Rf values, aiding in different solvent systems. GC-MS analysis revealed the presence of 29 bioactive compounds with diverse pharmacological activities, including anti-inflammatory, antioxidant, analgesic and antimicrobial properties. Antimicrobial effect of I. hochstetteri Baker methanolic extract showed significant inhibitory effects against E. coli, E. aerogenes, S. flexneri, P. aeruginosa, S. aureus, E. faecalis, B. cereus, and fungal strain C. albicans. The methanol extract also showed significant antifungal activity by inhibiting the growth of Sclerotium rolfsii in food poisoning method. MTT assays revealed significant cytotoxic activity of methanolic extract against human leukemia HL-60 cancer cells with IC50 of 116.01 μg/mL. In apoptotic study, I. hochstetteri Baker methanolic extract showed 28.84% viable cells, 30.2% early apoptosis, 35.54% late apoptosis, and 5.86% necrosis comparatively similar with standard used. The extract showed significant anti-inflammatory effect on HRBC stabilization, and protein denaturation of BSA and egg albumin denaturation with IC50 of 193.62 μg/mL, 113.94 μg/mL respectively. In anti-diabetic assays like α-amylase, α-glucosidase, and Glucose uptake assay, I. hochstetteri extract showed good anti-diabetic effect with IC50 of 60.64 μg/mL, 169.34 μg/mL, and 205.63 μg/mL respectively. In conclusion I. hochstetteri Baker have promising bioactive metabolites with significant biological activities, it can be good substitute for the chemical drugs after successful clinical studies.

A microchip gas chromatography column assembly with a 3D metal printing micro column oven and a flexible stainless-steel column

In this work, a microchip gas chromatography (GC) column assembly utilizing a three-dimensional (3D) printed micro oven and a flexible stainless steel capillary column was developed. The assembly's performance and separation capabilities were characterized. The key components include a 3D printed aluminum plate (7.50 × 7.50 × 0.16 cm) with a 3-meter-long circular spiral channel, serving as the oven, and the column coiled on the channel with an inner diameter of 320 μm and a stationary phase of OV-1. A heating ceramic plate was affixed on the opposite side of the plate. The assembly weighed 40.3 g. The design allows for easy disassembly, or stacking of heating devices and columns, enabling flexibility in adjusting column length. When using n-C13 as the test analyte at 140 °C, a retention factor (k) was 8.5, and 7797 plates (2599 plates/m) were obtained. The assembly, employing resistance heating, demonstrated effective separation performance for samples containing alkanes, aromatics, alcohols and ketones, with good reproducibility. The reduction in theoretical plates compared to oven heating was only 2.95 %. In the boiling point range of C6 to C18, rapid temperature programming (120 °C/min) was achieved with a power consumption of 119.512 W. The assembly was successfully employed to separate benzene series compounds, gasoline and volatile organic compounds (VOCs), demonstrating excellent separation performance. This innovative design addresses the challenges of the complexity and low repeatability of the fabrication process and the high cost associated with microchip columns. Furthermore, its versatility makes it suitable for outdoor analysis applications.

Optimization of Culturing Conditions for the Production of Antimicrobial Metabolite by Bacillus Carotarum

Forest soil antagonistic bacteria Bacillus carotarum was isolated and tested for optimum antimicrobial metabolite production. Maximum antimicrobial metabolite production was found at temperature 30°C and pH 7.0 and on Ist day of incubation at stationary condition. The medium consisting of beef extract - 0.3%, peptone - 0.5% and NaCl - 0.05%, was screened out as a suitable medium for maximum antimicrobial production supplemented individually with four carbon sources of which starch was found as the best carbon source. The active agent was best extracted with petroleum ether. Homogeneity of the crude bioactive metabolites were also tested by paper chromatographic analysis where a single type of bioactive metabolite was found with a Rf value of 0.94 in the solvent system n- butanol: acetic acid : water = 4 : 1 : 5 . The antimicrobial spectrum of the metabolite was wide and showed activity against Shigella dysenteriae (AE14612), Salmonella typhi(AE14296), Vibrio cholerae (A214748), Pseudomonas aeruginosa (CRL, ICDDR’ B), Bacillus cereus (BTCC19), and Bacillus subtilis (BTTC17). The Chittagong Univ. J. B. Sci. 8(1&amp;2): 01-10, 2013

Chiral Hydroxy Metabolite of Mebendazole: Analytical and Semi-Preparative High-Performance Liquid Chromatography Resolution and Chiroptical Properties.

Mebendazole (MBZ) is a benzimidazole carbamate anthelmintic used worldwide for the treatment and prevention of parasitic disorders in animals and humans. A large number of in vivo and in vitro studies have demonstrated that MBZ also has anticancer activity in multiple types of cancers. After oral administration, the phenylketone moiety of MBZ is rapidly reduced to the hydroxyl group to form the chiral hydroxy metabolite (MBZ-OH). To the best of our knowledge, there is no information in the literature on the stereochemical course of transformation and the anthelmintic and antitumor activity of individual enantiomers of MBZ-OH. In the present study, we describe in detail the direct HPLC resolution of MBZ-OH on a 100 mm × 4.6 mm Chirapak IG-3 column packed with 3 μm silica particles containing amylose (3-chloro-5-methylphenylcarbamate) as a selector. At 25 °C and using pure methanol as the mobile phase, the enantioseparation and resolution factors were 2.38 and 6.13, respectively. These conditions were scaled up at a semi-preparative scale using a 250 mm × 10 mm Chiralpak IG column to isolate multi-milligram amounts of both enantiomeric forms of the chiral metabolite. The chiroptical properties of the collected enantiomers were determined and, through a theoretical study, were related to the more stable conformations of MBZ-OH. The first and second eluted enantiomers were dextrorotatory and levorotatory, respectively, in dimethylformamide solution. Finally, by recording the retention factors of the enantiomers as the water content in the water-acetonitrile mobile phases was progressively varied, U-shaped retention maps were generated, indicating a dual and competitive hydrophilic interaction liquid chromatography and reversed-phase liquid chromatography retention mechanism on the Chirapak IG-3 chiral stationary phase.

Dynamic changes in dissolved organic matter during transport of landfill leachate in porous medium.

The dynamic changes in dissolved organic matter (DOM) during the transport of landfill leachate (LL) in porous medium should be explored, considering the high levels of DOM in the LL of municipal solid waste. Column experiments were carried out at 25°C at a Darcy's flux of 0.29cm/h for 2722h to compare the transport of Cl-, ultraviolet absorbance at 254nm (UV254), chemical oxygen demand (COD), and dissolved organic carbon (DOC) in the simulated porous medium by using the CXTFIT2.1 code. Results showed that the convection-dispersion equation (CDE) could describe Cl- transport well. The high levels of λ and D could be highly correlated with the physicochemical properties of the porous medium. The transport of the studied DOM with evident aromatic character could be described appropriately by the CDE model with the first-order reaction assumption, considering the similar variation trends of UV254, COD, and DOC in the effluent during experiments. Specifically, the values of retardation factor (R) were in the following order: DOC > UV254 > COD, whereas the low values of the first-order decay coefficient (k1) for DOC and COD were still higher than that for UV254. High contents of humic-like substances in the DOM with complex toxic components resulted in the natural low removal efficiencies of COD, DOC, and UV254 (≤ 23%), which could be confirmed by the variations of fluorescence index (FI) and humification index (HIX) in the effluent. The results should be helpful in evaluating the environmental risk induced by the LL leakage in a landfill site.

Factor Influencing Employee Retention in Cooperatives in the City of Mati, Davao Oriental

The general objective of this study was to identify the factors that influence employee retention in the cooperatives in the City of Mati. Specifically, to addressed the following specific objectives; (a) to determine the socio-demographic profile of cooperative employees in the City of Mati, (b) to determine the potent and least factor in employee retention, (c) to examine the significant difference in potent and least factor when group according to their socio-demographic profile. Descriptive research design was utilized in the study. It selected 317 respondents using complete enumeration sampling technique. Questionnaires were uploaded to KoBoToolbox and used in data collection. Then analyzed using descriptive and inferential. Frequency count and percentage, EFA, and ANOVA were utilized and presented in a table. The findings of the study revealed that majority of the cooperative employees were males ages 41 years old and above with less than five years in service. Also, most of their services offered were agricultural products. However, four factors were identified. Base pay was the potent factor and shows significant difference when group by age and length of service. However, organizational values and policy was the least factor and shows significant difference when group by age.

Fractionation and Identification of Phenolic Compounds from Ethylacetate Fraction of Ageratum Conyzoides Methanolic Leaf Extract

Natural phenols are significant functional substances that are commonly present in plants and provide advantages for human health. Phenolics can be utilized for a variety of therapeutic applications, such as antioxidant, anti-inflammatory, antidiabetic, and antibacterial activities. This work aimed to fractionate and identify the phenolic compounds present in ethylacetate fractions of the methanolic leaf extracts of A. conyzoides. Fractionation and purification of the ethylacetate fraction using column chromatography and TLC, followed by FTIR and LC-MS for identification, were employed in this work. While the FTIR spectroscopy was used to identify the fractions with –OH functional group, LCMS was used to identify the phenolics. After fractionation and purification, six ethylacetate samples were obtained, each with different Rf values, of which three showed a pronounced presence of OH functional groups in phenolics. Subsequently, four phenolic compounds were identified: furocoumaric acid, liquiritin, isorhamnetin, and syringin. This research has demonstrated that ethylacetate fraction of A. conyzoides methanol leaf extract is a good source of the phenolic compounds: Furocoumaric acid, Liquiritin, Isorhamnetin, and syringin.

Biosurfactant production by Bacillus amyloliquefaciens, characterization and its potential applications

Aim: To identify indigenous bacteria responsible for producing biosurfactants in soil contaminated by oil and to investigate their potential uses in the fields of pharmaceuticals and environmental applications. Methodology: The microorganisms of oil-contaminated soil were isolated, screened, and identified using 16S rRNA gene sequencing. Bacillus amyloliquefaciens was utilized to produce biosurfactants, and were characterized by UV, TLC, FTIR, HPTLC, and GCMS analysis. Antibacterial activity, plant growth promotion, biocompatibility, and wound healing activity of surfactant were performed. Results: Six bacterial cultures (B1 to B6) were isolated from the soil samples collected from various locations in Kerala and Tamil Nadu. Among the isolates screened for biosurfactant production, Bacillus amyloliquefaciens exhibited the highest capacity for biosurfactant production, confirmed through 16S rRNA gene sequencing. The biosurfactant produced was identified as surfactin of lipopeptide nature, characterized by various analytical techniques: UV absorption at 400 nm, TLC and HPTLC (Rf value of 0.58), FTIR (prominent peak at 3819 cm-1 corresponding to -OH groups), GCMS with a maximum retention time of 12.03. Surfactin effectively inhibited pathogenic bacteria, enhanced plant growth, was biocompatible, and enhanced the rate of cell migration towards wound scratch. Interpretation: The current study revealed that Bacillus amyloliquefaciens, isolated from oil-contaminated soil, is capable of producing biosurfactant surfactin. Additionally, it unveiled a broad spectrum of applications for surfactin, encompassing wound healing, biocompatibility, antimicrobial activity, and promotion of plant growth. Key words: Antibacterial activity, Biocompatibility, Bacillus amyloliquefaciens, Biosurfactant, Wound healing

Numerical modeling of PFAS movement through the vadose zone: Influence of plant water uptake and soil organic carbon distribution

In this study, we investigated the effects of soil organic carbon (SOC) distribution and water uptake by plant roots on PFAS movement in the vadose zone with a deep groundwater table under temperate, humid climate conditions. Two series of numerical simulations were performed with the HYDRUS computer code, representing the leaching of historical PFOS contamination and the infiltration of water contaminated with PFOA, respectively. We considered soil profiles with three distributions of SOC (no SOC, realistic SOC distribution decreasing with depth, and uniform SOC equal to the content measured in topsoil), three root distributions (bare soil, grassland, and forest), and three soil textures (sand, sandy loam, and loam). The SOC distribution had a profound impact on the velocity of PFOS movement. The apparent retardation factor for realistic SOC distribution was twice as large as for the scenario with no SOC and more than three times smaller than for the scenario with uniformly high SOC content. We also showed that the root distribution in soil profoundly impacts the simulations of PFAS migration through soil. Including the root zone significantly slows down the movement of PFAS, primarily due to increased evapotranspiration and reduced downward water flux. Another effect of water uptake by plant roots is an increase of PFAS concentrations in soil water (evapo-concentration). The evapo-concentration and the slowdown of PFAS movement due to root water uptake are more significant in fine-textured soils than in sand.