Catalytic green synthesis of Tin(IV) oxide nanoparticles for phenolic compounds removal and molecular docking with EGFR tyrosine kinase.

In this study, tin dioxide nanoparticles (SnO2 NPs) were successfully synthesized through an eco-friendly method using basil leaves extract. The fabricated SnO2 NPs demonstrated significant adsorption capabilities for phenol (PHE), p-nitrophenol (P-NP), and p-methoxyphenol (P-MP) from water matrices. Optimal conditions for maximum removal efficiency was determined for each phenolic compound, with PHE showing a remarkable 95% removal at a 3 ppm, 0.20 g of SnO2 NPs, pH 8, and 30 min of agitation at 35 °C. Molecular docking studies unveiled a potential anticancer mechanism, indicating the ability of SnO2 NPs to interact with the epidermal growth factor receptor tyrosine kinase domain and inhibit its activity. The adsorption processes followed pseudo-second order kinetics and Temkin isotherm model, revealing spontaneous, exothermic, and chemisorption-controlled mechanisms. This eco-friendly approach utilizing plant extracts was considered as a valuable tool for nano-sorbent production. The SnO2 NPs not only exhibit promise in water treatment and also demonstrate potential applications in cancer therapy. Characterization techniques including scanning electron microscopy, UV-visible spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction spectroscopy (XRD), and energy-dispersive X-ray spectroscopy (EDAX) provided comprehensive insights into the results.

Neodymium adsorption from aqueous solution by ß-cyclodextrin nanosponges and a polymer valorized from potato peels waste: experiments and conventional and statistical physics interpretations.

Using organic waste and residue streams to be turned into valuable and greener materials for various applications has proven an efficient and suitable strategy. In this work, two green materials (nanosponges and a polymer) were synthesized using potato peels and applied for the first time to adsorb and recover Neodymium (Nd3+) from aqueous solutions. The recovery of Nd3+ that belongs to the rare earth elements has attracted important interest due to its/their importance in several industrial and technological applications. The fine potato peel waste (FPPW) polymer presented an irregular shape and porous surface. At the same time, the ß-cyclodextrin (ß-CD) nanosponges had uniform distribution with regular and smooth shapes. ß-CD nanosponges exhibited a much higher total carboxyl content (4.02 mmol g-1) than FPPW (2.50 mmol g-1), which could impact the Nd3+ adsorption performance because carboxyl groups can interact with cations. The adsorption capacity increased with the increase of the pH, reaching its maximum at pHs 6-7 for ß-CD nanosponges and 4-7 for FPPW polymer. The kinetic and equilibrium data were well-fitted by General order and Liu models. ß-CD nanosponges attained adsorption capacity near 100 mg Nd per gram of adsorbent. Thermodynamic and statistical physical results corroborated that the adsorption mechanism was due to electrostatic interaction/complexation and that the carboxyl groups were important in the interactions. ß-CD nanosponges (three cycles of use) were more effective than FPPW (one cycle of use) in the regeneration. Finally, ß-CD nanosponges could be considered an eco-friendly adsorbent to recover Nd3+ from aqueous matrices.

Recovery and separation of glycyrrhizic acid from Natural Deep Eutectic Solvent (NADES) extract by macroporous resin: adsorption kinetics and isotherm studies.

Natural Deep Eutectic Solvents (NADESs) have emerged as a green and sustainable alternative to conventional organic solvents to extract bioactive compounds. However, the recovery of bioactive compounds from the NADES extracts is challenging, restricting their large-scale applications. The present work investigated the recovery of glycyrrhizic acid (GA) from choline-chloride/lactic acid NADES extract using macroporous resins. GA possesses a wide spectrum of biological activities, and it is extracted from the well-known herb Glycyrrhiza glabra. During resin screening, DIAIONTM SP700 showed high adsorption and desorption capacities. The adsorption kinetics study demonstrated that the adsorption of GA on SP700 followed Pseudo First-order kinetic model. Moreover, the adsorption behaviors were elucidated by the Freundlich isotherm using a correlation coefficient based on a static adsorption study at different temperatures and pH. Furthermore, the thermodynamic parameters, for instance, the change of Gibbs free energy (ΔG*), entropy (ΔS*), and enthalpy (ΔH*), showed that the adsorption process was spontaneous, favorable and exothermic. In addition, the sample after macroporous resin treatment, which is enriched with GA exhibited good anticancer potential analyzed by SRB assay. The regenerated NADES solvent was recycled twice, keeping more than 90% extraction efficiency, indicating good reusability of NADES in the GA extraction process by using macroporous resin.

Biosorption of U(VI) and mechanisms by live and dead cells of Sphingopyxis sp. YF1.

Heavy metal pollution seriously threatens the environment and human health. The biosorption of heavy metals has attracted worldwide attention due to its cost-effectiveness and environmental friendliness. It is significant to develop biosorbents with excellent adsorption performance. Sphingopyxis is widely used in the removal of various organic pollutants, but its potential application in heavy metal adsorption has been largely overlooked. This study investigates the biosorption of U(VI) onto live and dead cells of a Sphingopyxis strain YF1. The effects of pH, contact time and initial ion concentration on U(VI) adsorption investigated, and kinetic and isothermal models were used to fit the adsorption results. The results show that under pH 3-6, the adsorption of U(VI) by YF1 live cells increased with the increase of the pH. Both the pseudo-first order and pseudo-second order models can satisfactorily interpret the adsorption by live and dead cells. Three isothermal adsorption models (Langmuir, Freundlich, and Sips) were used to fit the adsorption process. The adsorption of uranium by live and dead cells was best fitted by the Sips model. The maximal adsorption capacities of U(VI) by live and dead cells were 140.7 mg g-1 and 205.7 mg g-1, respectively. The mechanisms of U(VI) adsorption by Sphingopyxis sp. YF1 were revealed. Scanning electron microscopy and energy dispersive spectroscopy (SEM-EDS) show that U(VI) was deposited on the surface of the bacterial cells. Fourier-transform infrared spectroscopy (FTIR) shows that amine, hydroxyl, alkyl, amide I, amide II, phosphate, carboxylates and carboxylic acids were the major functional groups that are involved in U(VI) adsorption by live and dead cells. X-ray photoelectron spectroscopy (XPS) suggests that the main functional groups of live cells involved in adsorption were O = C-O, C-OH/C-O-C and N-C = O. This study indicates Sphingopyxis sp. YF1 is a high-efficiency U(VI)-adsorbing strain, promising to remove U(VI) from aquatic environment.

Yttrium-modified drinking water treatment residue for efficient phosphorus removal: efficacy, mechanism, and reproducibility.

The excessive presence of phosphate can cause eutrophication in water bodies. Yttrium has an extremely high affinity for phosphorus and is capable of forming stable complexes at low concentrations. Moreover, limitations in the resourcefulness of drinking water treatment residues were observed. In this study, a highly efficient phosphorus removal adsorbent (RJDWTR@Y) was prepared by calcination-alkali leaching-yttrium-loaded composite modification employing domestic drinking water treatment residue as raw material. And the effects of multiple factors on phosphate adsorption by RJDWTR@Y were examined. The results illustrated that the maximum adsorption capacity of the RJDWTR@Y for phosphate was 319.76 mg/g, with the chemical reaction of the multilayer as the predominant adsorption process. The adsorption mechanism is electrostatic gravitational force and the inner sphere complexation effect. RJDWTR@Y was effective against interference even at high concentrations of the coexisting anion. After five cycles, the desorption efficiency of phosphate was 75.11%. Filling the fixed bed with the material can efficiently remove phosphorus from the flowing liquid. The synthesis of RJDWTR@Y and the results of the study indicated that it has good application prospects. In addition to efficiently removing phosphorus, it can also recycle waste and achieve sustainability.

Capillary electrokinetic chromatography for studying interactions between ß-blockers and Intralipid emulsion.

Toxicity of ß-blockers is one of the most common causes of poison-induced cardiogenic shock throughout the world. Therefore, methodologies for in vivo removal of the drugs from the body have been under investigation. Intralipid emulsion (ILE) is a common commercial lipid emulsion used for parenteral nutrition, but it has also been administered to patients suffering from drug toxicities. In this work, a set of ß-blockers of different hydrophobicity's (log KD values ranging from 0.16 to 3.8) were investigated. The relative strength of the interactions between these compounds and the ILE was quantitatively assessed by means of binding constants and adsorption constants of the formed ß-blocker-ILE complexes. The binding constants were determined by capillary electrokinetic chromatography and the adsorption constants were calculated based on different adsorption isotherms. Expectedly, the binding constants were strongly related to the log KD values of the ß-blockers. The binding and adsorption constants also show that less hydrophobic ß-blockers interact with ILE, suggesting that this emulsion could be useful for capturing such compounds in cases of their overdoses. Thus, the use of ILE for treatment of toxicities caused by a larger range of ß-blockers is worth further investigation.

New ion-imprinted polymer for selective removal of Cu2+ ion in aqueous solution using extracted Aloe vera leaves as a monomer.

The objective of this project is to create a unique type of polymer known as an ion imprinted polymer (IIP) and a non-imprinted polymer (NIP) utilizing natural waste biosorbent materials. One example of this type of waste is Aloe vera, a plant with many medicinal uses that is grown globally. Aloe vera is considered one of the most valuable medicinal plants with a wide range of applications. Extracted Aloe vera was used as functional monomers for the first time to prepare new IIPs, epichlorohydrin, and Cu2+ ion as the cross-linking agent and template, respectively. The NIP was also synthesized for comparison, without the use of the Cu2+ salt. Following polymerization, the IIP particles were cleansed of template ions through a 0.1 M EDTA leaching process, resulting in the formation of cavities within the particles, these cavities in the polymer provide selective linking zones for these specific template ions. The synthesized IIPs were characterized using the most recent identification instruments. The experimental parameters for adsorption, such as pH of a solution, contact time, initial copper concentration, adsorbent dosage, and temperature have been optimized. The most effective conditions for metal adsorption onto the ionic imprinted polymer were found to be a pH of 8.0, a temperature of 30 °C, a concentration of 0.03 g/100 mL, and a contact time of 50 min. Based on the ANOVA statistical value, the adsorption of Cu2+ ion on IIP is significant with very low probability (p) values (<0.001). The Langmuir isotherm model and a second-order reaction were both used in the adsorption process. According to thermodynamic characteristics, Cu2+ adsorption over IIPs and NIP was an endothermic, spontaneous process. Compared to NIP, the imprinted polymer exhibits a significantly better capacity and selectivity for Cu2+ adsorption, the maximum removal percentage of IIPs and NIP was 96.02 % and 74.3 % respectively. Moreover, the research showed that ion imprinting can be a promising technique for preparing selective adsorbents to separate and preconcentrate metal in a medium of multiple competitive metals (Co2+, Cd2+, Ni2+, Zn2+, Fe2+, and Pb2+) The most important point for this new Cu2+-IIPs was shown superior reusability up to 8 cycles with small decrees in uptake capability.

Enhanced adsorption of ceftriaxone antibiotics from water by activated carbon derived from agriculture products waste.

The present work determines efficiency of domestic food waste like tea waste in removing pharmaceutical waste such as ceftriaxone (CEF) from synthetic wastewater. Carbonaceous material; Tea waste activated carbon (TAC) has been employed and it showed high removal capacity of 787.5 mg/g. TAC was characterized using; XPS, XRD, SEM, FT-IR, and BET as well as it approved that the adsorbent a has high surface area of .6 m2 /g. Various experimental parameters are evaluated for the removal efficiency of the synthesized adsorbent under the present study. During the adsorption study through batch experiments, it approved that the adsorption isotherm was fitted to Langmuir, while kinetically fitted to pseudo-second-order; the adsorption process was chemisorption process as the adsorption energy was 23.7 kJ mol-1 . From evaluation thermodynamic parameters the adsorption reaction was endothermic and spontaneous reaction. The different real samples spiked with CEF and studies the efficiency of TAC to remove it. On the other hand, investigated the regeneration efficiency of the TAC and exhibit high regeneration efficiency as it will be used after four cycles with good efficiency of about 84.2%.

Heteropolysaccharides in sustainable corrosion inhibition: 4E (Energy, Economy, Ecology, and Effectivity) dimensions.

Carbohydrate polymers (polysaccharides) and their derivatives are widely utilized in sustainable corrosion inhibition (SCI) because of their various fascinating properties including multiple adsorption sites, high solubility and high efficiency. Contrary to traditional synthetic polymer-based corrosion inhibitors, polysaccharides are related to the 4E dimension, which stands for Energy, Economy, Ecology, and Effectivity. Furthermore, they are relatively more environmentally benign, biodegradable, and non-bioaccumulative. The current review describes the SCI features of various heteropolysaccharides, including gum Arabic (GA), glycosaminoglycans (chondroitin-4-sulfate (CS), hyaluronic acid (HA), heparin, etc.), pectin, alginates, and agar for the first time. They demonstrate impressive anticorrosive activity for different metals and alloys in a variety of corrosive electrolytes. Through their adsorption at the metal/electrolyte interface, heteropolysaccharides function by producing a corrosion-protective film. In general, their adsorption follows the Langmuir isotherm model. In their molecular structures, heteropolysaccharides contain several polar functional groups like -OH, -NH2, -COCH3, -CH2OH, cyclic and bridging O, -CH2SO3H, -SO3OH, -COOH, -NHCOCH3, -OHOR, etc. that serve as adsorption centers when they bind to metallic surfaces.

A model for predicting reduction in mobile phosphorus of lake sediment by aluminum drinking water treatment residuals.

Drinking water treatment residual (DWTR) derived from flocculation and sedimentation of raw water using aluminum coagulants is a valuable environmental remediation byproduct capable of inactivating phosphorus (P). However, no generalizable model exists in the literature to describe reduction of releasable (mobile) P in lake sediment as a result of DWTR addition. The reduction of mobile P (sum of labile P and reductant soluble P) was investigated in over 100 sub-samples using five sediment samples from two lakes and three DWTRs from different water treatment plants. A consistent relationship was determined across a range of mobile P contents (0.23 g/m2/cm to 0.92 g/m2/cm, or 15.8 to 186.1 µg/g DW) and DWTRs. The relationship was best described as a function of the mobile P content of the sediment and the oxalate-extractable aluminum content of the DWTR. An empirical model was developed to predict the immediate reduction in mobile P following the addition of DWTR containing aluminum. This model was validated using two additional lake sediments and one additional DWTR (R² = 0.995). Thus, the immediate inactivation of P in lake sediment following DWTR addition can be predicted with this model, which can be used with internal P loading or other water quality goals to determine an appropriate DWTR dose. Further recommendations were made about dosing DWTRs for lake restoration, allowing practitioners to use DWTR to inactivate P in lake sediment without conducting individual sorption experiments.

Study of Interactions between Saponin Biosurfactant and Model Biological Membranes: Phospholipid Monolayers and Liposomes.

The aim of this study was to determine the effect of saponins-rich plant extract on two model biological membranes: phospholipid monolayers and liposomes. The Langmuir monolayer technique was used to study the interactions of model phospholipid membranes with saponins. The π-A isotherms were determined for DPPE (1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine) monolayer with the addition of various concentrations of licorice saponins extracts and subjected to qualitative as well as quantitative analysis. Additionally, relaxation studies of the obtained monolayers were carried out and morphological changes were examined using Brewster angle microscopy. Moreover, changes in the structure of phospholipid vesicles treated with solutions of saponins-rich plant extracts were assessed using the FTIR technique. The size and zeta potential of the liposomes were estimated based on DLS methods. The obtained results indicated that the saponins interact with the phospholipid membrane formed by DPPE molecules and that the stability of the mixed DPPE/saponins monolayer strongly depends on the presence of impurities in saponins. Furthermore, it was found that the plant extract rich in saponins biosurfactant interacts mainly with the hydrophilic part of liposomes.

Preparation of alumina-supported Fe-Al-La composite for fluoride removal from an aqueous matrix.

Using groundwater for human consumption is an alternative for places with no nearby surface water resources. Fluoride is commonly found in groundwater, and the consumption of this water for a prolonged time in concentrations that exceed established limits by WHO and Brazilian legislation on water potability (1.5 mg L-1) can cause harmful problems to human health. For this reason, fluoride removal is an important step before water consumption. In this work, activated alumina was impregnated with Fe-Al-La composite and employed for the first time as an adsorbent for fluoride removal from an aqueous environment. XRD, SEM/EDS, FT-IR, and point of zero charge were used to characterize the prepared adsorbent. The adsorptive performance of adsorbent material was investigated by employing a 23-central composite design (CCD), and the obtained experimental conditions were pH = 6.5 and adsorbent dosage = 3.0 g L-1. A maximum adsorption capacity of 8.17 mg g-1 at 298 K and pH = 6.5 was achieved by Langmuir isotherm to describe the adsorption. The kinetic model that better described experimental data was Avrami, with the kav parameter increasing with the initial concentration from 0.076 to 0.231 (min-1)nav. The nature of adsorption was found to be homogeneous, and it occurs in a monolayer. The fluoride removal performance for the prepared adsorbent was higher than granular activated alumina, showing that supporting Fe-Al-La at the alumina surface increased its fluoride adsorption capacity from 16 to 42% at the same experimental conditions. Finally, the influence of co-existing ions Cl-, SO42-, and NO3- was evaluated in fluoride adsorption, and the material presented great selectivity to fluoride. Thus, Fe-Al-La/AA adsorbent is a promising material for fluoride removal from water.

Removal of methylene blue dye from aqueous solution using an efficient chitosan-pectin bio-adsorbent: kinetics and isotherm studies.

Wastewater contains organic compounds, including dyes, which have potential risks to the environment. Hence, these compound needs to be eliminated from the aqueous solution. In the present study, chitosan-pectin composite (Cs-Pc) was used as an adsorbent to remove methylene blue dye (MB) from synthetic wastewater. To evaluate the parameters affecting adsorption, including the initial MB concentration, solution pH, contact time, and Cs-Pc dose, batch experiments were carried out. Scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), Fourier transform infrared (FTIR), and pH point of zero charges (pH pzc) were applied for characterizations of Cs-Pc. The optimum conditions were obtained with an initial MB concentration of 50 mg L-1: solution pH ~ 11, Cs-Pc dose: 1.5 g L-1 and 180 min contact time, which caused 97.77% of MB removal. In addition, the removal efficiency of MB was more influenced by pH than by sorbate dose. Also, Cs-Pc had a higher ability to remove MB than chitosan and pectin, probably due to its highly porous structure and rough surfaces that provides active sites and facilitate MB adsorption. The maximum removal efficiency and the adsorption capacity of MB onto Cs-Pc at 500 mg L-1 concentration under optimum conditions were 98.67% and 328.02 mg g-1, respectively. The adsorption kinetics and isotherms were best described by pseudo-second-order and Freundlich equation, respectively. After four times of recycling, the removal efficiency of MB was above 96%. Electrostatic and pi-pi interactions are the main mechanisms for the removal of MB onto the adsorbent. So the application of Cs-Pc is promising for MB removal from polluted solutions not only due to its strong adsorbing capability but also due to its excellent ability to reuse.

Green synthesis of Ag2O nanoparticles using Punica granatum leaf extract for sulfamethoxazole antibiotic adsorption: characterization, experimental study, modeling, and DFT calculation.

Silver oxide (Ag2O) nanoparticles (NPs) were generated by synthesizing green leaf extract of Punica granatum, and afterwards they were used as adsorbent to remove the antibiotic additive sulfamethoxazole (SMX) from aqueous solutions. Prior of their use as adsorbent, the Ag2O NPs were characterized by various methods such as X-ray diffraction, Fourier transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET), scanning electron microscopy/energy-dispersive X-ray (SEM-EDX), and transmission electron microscopy (TEM). The Ag2O NPs were found to be spherically shaped and stabilized by the constituents of the extract. Further, at SMX antibiotic concentration of 100 mg L-1, the Ag2O NPs achieved almost complete removal of 98.93% within 90 min, and by using 0.8 g L-1 of adsorbent dose at pH=4 and temperature T=308 K. In addition, the experimental data were well fitted with the theoretical Langmuir model indicating homogeneous adsorbed layer of the SMX antibiotic on the Ag2O NPs surface. The maximum uptake capacity was 277.85 mg g-1. A good agreement was also found between the kinetic adsorption data and the theoretical pseudo-second-order model. Regarding the thermodynamic adsorption aspects, the data revealed an endothermic nature and confirmed the feasibility and the spontaneity of the adsorption reaction. Furthermore, the regeneration study has shown that the Ag2O NPs could be efficiently reused for up to five cycles. The geometric structures have been optimized and quantum chemical parameters were calculated for the SMX unprotonated (SMX+/-) and protonated (SMX+) using density functional theory (DFT) calculation. The DFT results indicated that the unprotonated SMX+/- reacts more favorably on the Ag2O surface, as compared to the protonated SMX+. The SMX binding mechanism was predominantly controlled by the electrostatic attraction, hydrogen bond, hydrophobic, and π-π interactions. The overall data suggest that the Ag2O NPs have promising potential for antibiotic removal from wastewater.

Thiosulfate impregnated spent tea leaves for the remarkable uptake of malachite green.

Herein we demonstrate an enhanced performance of acid-assisted thiosulfate-impregnated spent/waste tea leaves (TWTL) for the removal of malachite green (MG) from water by batch mode. The material was characterized by pHZPC, FTIR, powder XRD, SEM, and proximate analysis. FTIR suggests the presence of polyphenolic moieties whereas a lignocellulosic peak was observed in powder XRD. SEM image shows a grafted surface texture with intermittent blocks, which upon dye uptake becomes somewhat condensed. Under optimized conditions, the highest removal efficiency of 126.8 mg/g was achieved at pH 7. A fast adsorption process was noticed with >97% removal within the first 10 min. Adsorption follows pseudo-second-order kinetics (R2 = 0.999) and the Langmuir model (R2 = 0.999). The material can be regenerated by dilute hydrochloric acid and can be reused for up to four cycles. Treatment of industrial effluent was successful in up to 47.56%. Our results highlight the potential of thiosulfate-treated spent tea leaves as a choice for the efficient removal of malachite green from water.

Tea, being one of the most popular beverages produces huge waste which requires proper management. With this aim; the thiosulfate-impregnated spent tea leaves have been exercised for effective separation of malachite green from contaminated water. Thiosulfate impregnation under mildly acidic conditions activates the tea leaves and makes the material robust with enhanced water stability than its untreated variety. With a remarkable maximum adsorption capacity of 126.8 mg/g under ambient conditions, the present methodology enjoys the edge over related phytosorbents. The protocol is techno-economic, environment friendly, and could be extended to possible field applications.

Environmental remediation of selenium using surface modified carbon nano tubes - Characterization, influence of variables, equilibrium and kinetic analysis.

Selenium is targeted as a priority pollutant to be removed due to its high toxicity level and lethal effects. In this research, a novel nano sorbent was fabricated using ionic liquid on multiwalled carbon nanotubes (IL-MCNT) and employed for Selenium remediation from aqueous media. Besides solution pH, nanocomposite dosage, the initial selenium concentration, temperature and sorption time were also examined as operating variables. At optimal pH 2.0, 96% of the selenium was removed with maximum efficiency with 100 mg/L of IL-MCNT at 308 K, 45 min of contact time, and 110 g of IL-MCNT dosage. From kinetic studies, it appears that the Langmuir isotherm fits the observed data (R2 > 0.9813), supporting the hypothesis that monolayer attachment occurs. The Langmuir isotherm parameters are evaluated as qm = 125 mg/g and KL = 0.172 L/mg. As a result of testing several kinetic models, the pseudo-second-order model was the most suitable for experimental data (R2 > 0.9746). Scanning Electron Microscopy images, FTIR spectra, and thermogravimetric study were used to examine the synthesized nanomaterial.

Efficient removal of total arsenic (As3+/5+) from contaminated water by novel strategies mediated iron and plant extract activated waste flowers of marigold.

In this investigation, marigold flower-waste was activated with iron salts (MG-Fe), subsequently marigold plant extract (MG-Fe-Ex) for the adsorptive elimination of As3+ and As5+ from contaminated water. The governing factor such as medium pH, temperature, pollutant concentration, reaction time, adsorbent dose were considered for the study. The complete elimination of As3+/5+ was recorded with MG-Fe-Ex at pH 8.0, 90 min, 30 °C, dose 4 g/L, 20 mg/L of As3+/5+ and shaking rate 120 rpm, while under the identical experimental condition, MG-Fe exhibited 98.4% and 73.3% removal for As5+ and As3+, respectively. The MG-Fe-Ex contains iron oxides (Fe2O3 and Fe3O4) as a result of iron ions reaction with plant bioactive molecules as evident from x-ray diffraction analysis (XRD), energy dispersive x-ray spectroscopic (EDS) and Fourier transform infrared (FTIR) spectroscopic study. The adsorption data of As3+/5+ on MG-Fe and MG-Fe-Ex was best fitted by pseudo-first order kinetic and freundlich isotherm except As5+ adsorption on MG-Fe-Ex that can be described by langmuir isotherm model. The prevailing mechanism in adsorption of As3+/5+ on both adsorbent might be hydrogen bonding, electrostatic attraction and complexation. From the above, it is confirmed that MG-Fe-Ex adsorbent has high potential and can be used for the adsorptive elimination of As3+/5+ from contaminated water in sustainable and environmentally friendly way.

Effects of Piptoporus betulinus Ethanolic Extract on the Proliferation and Viability of Melanoma Cells and Models of Their Cell Membranes.

Piptoporus betulinus is a fungus known for its medicinal properties. It possesses antimicrobial, anti-inflammatory, and anti-cancer activity. In this study, several tests were performed to evaluate the cytotoxic effect of the ethanolic extract of Piptoporus betulinus on two melanoma human cell lines, WM115 primary and A375 metastatic cell lines, as well as Hs27 human skin fibroblasts. The extract proved to affect cancer cells in a dose-dependent manner, and at the same time showed a low cytotoxicity towards the normal cells. The total phenolic content (TPC) was determined spectrophotometrically by the Folin-Ciocalteu method (F-C), and the potential antioxidant activity was measured by ferric-reducing antioxidant power (FRAP) assay. One of the active compounds in the extract is betulin. It was isolated and then its cytotoxic activity was compared to the results obtained from the Piptoporus betulinus extract. To further understand the mechanism of action of the extract's anticancer activity, tests on model cell membranes were conducted. A model membrane of a melanoma cell was designed and consisted of 1,2-dimyristoyl-sn-glycero-3-phosphocholine, disialoganglioside-GD1a and cholesterol: DMPC:GD1a:chol (5:2:3 mole ratio). Changes in a Langmuir monolayer were observed and described based on Π-Amol isotherm and compressibility modulus changes. LB lipid bilayers were deposited on a hydrophilic gold substrate and analyzed by IR and X-ray photoelectron spectroscopy. Our study provides new data on the effect of Piptoporus betulinus extract on melanoma cells and its impact on the model of melanoma plasma membranes.

Synthesis of metal-based functional nanocomposite material and its application for the elimination of paracetamol from synthetic wastewater.

Non-steroidal anti-inflammatory medicines (NSAIDs) like paracetamol and other substances released into the water system pose serious environmental issues. The current work examines the synthesis of a nanocomposite combined with Moringa olifera aqueous leaf extract as a reducing and stabilizing agent for the green synthesis of nanocomposites. Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (XRD), Thermogravimetric analysis (TGA), Scanning Electron Microscope (SEM), Transmission Electron Microscope (TEM) were used to investigate metal based functional nanocomposites. The absorption band centered at a wavelength of 243 nm, which corresponds to the surface plasmon resonances of the produced nanocomposite, is confirmed in UV-vis spectra. The distinctive band at this particular wavelength is attributed to a particular group of nanocomposites based on the result from the Fourier transform infrared spectroscopy spectra. The spherical with irregularly shaped aggregates was confirmed by transmission electron microscopy, and the average size of nanoparticles was found to be 1 nm. For the elimination of pharmaceutical contaminants such as paracetamol from aqueous solutions, the adsorptive characteristics of nanocomposites were examined. Temperature, pH, adsorbent dosage, and agitation speed were investigated as adsorption parameters using Box-Behnken Design (BBD). The best removal outcomes were found under the following circumstances: temperature at 303.15 K, pH = 7.5, 0.05 g of nanocomposites at 200 rpm. Based on the adsorption study, the kinetics was found to be pseudo first order (R2 > 0.9481) which was validated and fitted by Langmuir isotherm (R2 > 0.9973). The adsorption study confirms that it was adsorbed onto the synthesized nanocomposite and found to be present on the homogeneous surface.

Wastewater irrigation: An opportunity for improving soil phosphorus availability; PHREEQC modeling and adsorption studies.

Wastewater, an alternative supply of water and nutrients, is being allocated as a priority for human population sustainability in arid and semi-arid regions. This work proposes phosphorus (P), a vital growth-limiting nutrient, adsorption behavior in wastewater irrigated agricultural soils in comparison to non-irrigated soils using laboratory batch experiments. The adsorption mechanism was assessed using different adsorption isotherm models. Saturation indices were modeled, using the hydro-geochemical transport code PHREEQC and MINTEQ geochemical software. Phosphorus buffering parameters were also calculated based on the standard equations. The equilibrium data were well fitted with the Freundlich isotherm model. The physical adsorption mechanism was found based on the calculated isotherm parameters. The maximum adsorption capacity was two times more in non-wastewater irrigated soils than irrigated. Results highlighted the effectiveness of wastewater irrigation in P availability in soil. Based on the PHREEQC modeling data, precipitation of Pb and Zn mineral phases was probable in soils by wastewater influence. Meanwhile, the precipitation of stable calcium phases, that affect the P sorption and/or co-precipitation, in non-wastewater irrigated soils was highlighted in the PHREEQC calculations. The standard buffer capacity (SBC) was 43 and 64 L kg-1 in wastewater irrigated soils and non-irrigated soils, respectively. Findings of the present study demonstrate the importance of wastewater reuse opportunities for agricultural application, especially soil P availability, and are helpful to minimize the environmental impacts of wastewater and solid waste.