Exploring Cold plasma technology: Enhancements in Carob seed germination, phytochemical Composition, and antioxidant activity.

The cultivation of carob tree does not need many climatic and ecological requirements. The main limit to its large-scale cultivation is the defects for propagation with seeds. Addressing this, our study evaluated the effect of cold plasma pretreatment on carob seed germination. Impressively, cold plasma showcased beneficial effects by significantly increasing water uptake in seeds (CS: 1.71 ± 0.59; PS/3.99 ± 1.56) and decreasing the contact angle from 80.7° to 57.9°, enhancing the seed surface's hydrophilicity. While the germination rate enhancement was subtle, the treatment presented an innovative route to modifying the seed's physiochemical properties. Specifically, storage proteins like albumin, globulin, and prolamin were notably reduced (Albumin (from 7.67 to 4.95 mg/g DW), Globulin (from 8.52 to 5.80 mg/g DW) and Prolamin (from 3.53 to 1.66 mg/g DW)). Additionally, there was a decline in the overall content of polyphenols (from 846.88 to 760.94 mg GAE/100g DW) and flavonoids (from 790.93 to 502.95 mg GAE/100g DW) and a decrease in the ferric reducing power (from 34.48 to 26.39 mg AAE/g DW). However, radical scavenging activity remained consistent. Intriguingly, FTIR-ATR spectral analysis post plasma treatment indicated oxidative alterations in the seed coat, marked by a distinctive intensity at 1732 cm⁻1. This investigation suggests that the application of eco-friendly technology could provide improvements in seed surface's hydrophilicity, but appropriate conditions could be chosen to increase germination efficiency.

Green solid-liquid extraction of cactus (Opuntia ficus-indica) cladode dietary fibers. I- optimization, pilot-scale production, and characterization.

In this research work, an optimization of an environment friendly extraction method of cactus (Opuntia ficus indica) cladode dietary fibers was conducted. For this purpose, a central composite experimental design with two factors (temperature and time) and five levels was established. The basic objective of this optimization was to maximize fiber yield using hot water as an extraction eco-solvent. The optimum extraction time (330 min) and temperature (100 °C) were determined with a constant medium agitation rate. Additionally, this study also aimed at establishing the validation of the statistical model to carry out the extrapolation of the extraction process at the pilot scale. The fibers extracted at the pilot scale showed yields (45.2 ± 0.01%) in agreement with those obtained through the optimization and validation lab-scale steps (44.97 ± 0.02). Fourier Transform Infrared (FTIR) spectroscopy, X-ray Diffraction (XRD) and Scanning electron microscopy (SEM) analysis were conducted to investigate the structure and microstructure of pilot scale-produced fibers. FTIR spectrum and XRD pattern were typical to lignocellulosic fibers results. Sharp and thin peaks characteristic of cellulose were detected. Pure and crystallized phases were recorded with a 45% crystallinity index. SEM analysis presented elongated and organized cells with a uniform structure comparable to cellulosic fibers microstructure.

An Overview of Recent Developments in Improving the Photocatalytic Activity of TiO2-Based Materials for the Treatment of Indoor Air and Bacterial Inactivation.

Indoor air quality has become a significant public health concern. The low cost and high efficiency of photocatalytic technology make it a natural choice for achieving deep air purification. Photocatalysis procedures have been widely investigated for environmental remediation, particularly for air treatment. Several semiconductors, such as TiO2, have been used for photocatalytic purposes as catalysts, and they have earned a lot of interest in the last few years owing to their outstanding features. In this context, this review has collected and discussed recent studies on advances in improving the photocatalytic activity of TiO2-based materials for indoor air treatment and bacterial inactivation. In addition, it has elucidated the properties of some widely used TiO2-based catalysts and their advantages in the photocatalytic process as well as improved photocatalytic activity using doping and heterojunction techniques. Current publications about various combined catalysts have been summarized and reviewed to emphasize the significance of combining catalysts to increase air treatment efficiency. Besides, this paper summarized works that used these catalysts to remove volatile organic compounds (VOCs) and microorganisms. Moreover, the reaction mechanism has been described and summarized based on literature to comprehend further pollutant elimination and microorganism inactivation using photocatalysis. This review concludes with a general opinion and an outlook on potential future research topics, including viral disinfection and other hazardous gases.

Synthesis and Characterization of TiO2 Nanotubes (TiO2-NTs) with Ag Silver Nanoparticles (Ag-NPs): Photocatalytic Performance for Wastewater Treatment under Visible Light.

In this work, we present the influence of the decoration of TiO2 nanotubes (TiO2-NTs) with Ag silver nanoparticles (Ag-NPs) on the photocatalysis of emerging pollutants such as the antibiotic diclofenac sodium. The Ag-NPs were loaded onto the TiO2-NTs by the anodization of metallic titanium foils. Diclofenac sodium is an emerging pollutant target of the pharmaceutical industry because of its negative environmental impact (high toxicity and confirmed carcinogenicity). The obtained Ag-NP/TiO2-NT nanocomposites were characterized by X-ray diffraction (XRD), photoluminescence spectroscopy (PL), scanning electron microscopy (SEM), transmission spectroscopy (TEM), and X-ray photoelectron spectroscopy (XPS). In order to study the photocatalytic behavior of Ag-NPs/TiO2-NTs with visible cold LEDs, the possible photocatalytic mechanism of antibiotic degradation with reactive species (O2°- and OH°) was detailed. Moreover, the Langmuir-Hinshelwood model was used to correlate the experimental results with the optimized catalyst. Likewise, reuse tests showed the chemical stability of the catalyst.

Modelization and implementation of free adsorption and electrosorption of Cr (VI) from wastewater using Al2O3 nanoparticles: assessment and comparison of the two processes.

The objective of this study was to apply the technique of electrosorption in order to assess the capacity of heterogeneous adsorption under an electric field. This was to enhance the adsorption capacity of the nanoparticles, to shorten the adsorption time, and to reduce the cost of the purification of contaminated waters. A final objective of this study was to compare the free adsorption (FA) and the electrosorption (ES) to understand the interface adsorbent/adsorbate at different contact conditions. For these purposes, a potentially efficient, environment-friendly absorbent was synthesized for dechromation purposes. The experimental design method generated optimum conditions as tc = 123 min, T = 318°K, and C0 = 100 mg/L. Freundlich's well-fitted modeling proved that the adsorption of chromate (VI) on nano-Al2O3 occurred on a homogenous surface. In addition, the adsorption coefficient intensity n did not only confirm monolayer adsorption but also indicated a favorable adsorption process. Thermodynamic studies confirmed the reaction spontaneity and the physisorption of the process. The electrosorption process was also tested using 20mA/cm2 as applied current density. Free-adsorption (FA) and electrosorption (ES) processes were compared. The maximum recorded yield was 99% for (EA) against 87% for (FA). EDS analysis recorded 11.3% of chromate adsorbate with free adsorption. The amount of Cr (VI) on nano-Al2O3 was 42.5 %. Nevertheless, the Al2O3 nanoparticles lost their crystallinity and exploded after the ES process. Mechanisms of both (FA) and (ES) were proposed.

Development of novel and ecological keratin/cellulose-based composites for absorption of oils and organic solvents.

Keratin/cellulose cryogels were successfully fabricated using chicken feathers (CF) and cardboard (C) from environmental waste for the first time, to be exploited in oil/solvent absorption. The keratin/cellulose-based composites were obtained by combining the dissolution of CF and C waste in 1-butyl-3-methylimidazolium chloride (Bmim-Cl+) ionic liquid green solvent via regeneration, simply by the freeze-drying method. The characterization analysis of the synthesized keratin/cellulose-based composites was performed using Fourier transform infrared spectrometry, X-ray diffractometry, scanning electron microscopy, and thermogravimetry. The as-prepared cryogel can absorb various oils and organic solvents. Moreover, its sorption capacity can reach up to 6.9-17.7 times the weight of the initial cryogel. This kind of CF/C cryogel revealed good and fast absorption efficiency. It could also be reused by simple absorption/distillation and absorption/desorption methods. Through the kinetic analysis, it was found that the pseudo-second-order model was more appropriate for the keratin/cellulose cryogel oil absorption process. Besides, owing to its low cost, good absorption capacity, and excellent reusability, this cryogel has potential for spill cleanup of oils and organic solvents.

Enhanced Cu(II) adsorption using sodium trimetaphosphate-modified cellulose beads: equilibrium, kinetics, adsorption mechanisms, and reusability.

The current study is focused on the simple synthesis of two novel biosorbent beads: BASB/STMP and CNFB/STMP, derived respectively from bleached almond shell (BAS) and cellulose nanofiber from almond shell (CNF) by means of chemical crosslinking with sodium trimetaphosphate (STMP). These biosorbents were thoroughly characterized in terms of structure (FTIR), texture (N2 adsorption-desorption), thermal behavior (TGA/DTG), morphology (SEM), and surface properties (XPS). The adsorption kinetics of Cu(II) ions onto BASB/STMP and CNFB/STMP materials proved the chemisorption interaction between Cu(II) ions and the STMP functionalized beads. The BASB/STMP equilibrium data were successfully described by the Redlich-Peterson model and the CNFB/STMP data by the Sips model which disclosed maximum adsorption capacities of 141.44 mg g-1 and 147.90 mg g-1, respectively. Furthermore, the BASB/STMP bioadsorbent offers easy regeneration and better reusability with high efficiency (> 83%). This study sheds light on the preparation of low-cost adsorbents for wastewater treatment in order to improve the competitiveness and eco-friendliness of agrowaste-based processes.

Optimization of synergistic biosorption of oxytetracycline and cadmium from binary mixtures on reed-based beads: modeling study using Brouers-Sotolongo models.

The first aim of this study was to synthesize and characterize reed-based-beads (BBR), an enhanced adsorbent from Tunisian reed. The second purpose was to evaluate and optimize the BBR efficiency for the simultaneous removal of oxytetracycline (OTC) and cadmium (Cd(II)), using central composite design under response surface methodology. The third goal was to elucidate the biosorption mechanisms taking place. It was shown that under optimum conditions (4.19 g L-1 of BBR, 165.54 µmol L-1 of OTC, 362.16 µmol L-1 of Cd(II), pH of 6, and 25.14-h contact time) the highest adsorption percentages (63.66% for OTC and 99.99% for Cd(II)) were obtained. It was revealed that OTC adsorption mechanism was better described by Brouers-Sotolongo fractal equation, with regression coefficient (R2) of 0.99876, and a Person's chi-square (χ2) of 0.01132. The Weibull kinetic equation better explained Cd(II) biosorption (R2 = 0.99959 and χ2 = 0.00194). FTIR and isotherm studies confirmed that the BBR surface was heterogeneous, and that adsorption mechanisms were better described by the Freundlich/Jovanovich equation (R2 = 0.99276 and χ2 = 0.04864) for OTC adsorption, and by the Brouers-Sotolongo model (R2 = 0.9851 and χ2 = 0.77547) for Cd(II) biosorption. Overall results indicate that, at last, the BBR lignocellulosic biocomposite beads could be considered as cost-effective and efficient adsorbent, which could be of socioeconomic and environmental relevance. Graphical abstract.

Calcination Improves the In Vivo Efficacy of a Montmorillonite Clay to Bind Aflatoxin G1 in Broiler Chickens: A Toxicokinetic Approach.

The goal of this study was to investigate the toxicokinetic characteristics of aflatoxin G1 (AFG1) in broiler chickens and the effect of calcination of a Tunisian montmorillonite clay on the in vivo absorption of AFG1. In this study, broiler chickens were randomly distributed into four groups of 10 animals. Group 1 was administered AFG1 (2 mg/kg body weight (BW)) by single intravenous injection (IV), group 2 received an intra-crop bolus (PO) of AFG1 without any clay, group 3 was dosed AFG1 PO together with an oral bolus of purified clay (CP), and group 4 received AFG1 PO with an oral bolus of calcined clay. A significant difference in the area under the curve (AUC0-t) was observed for group 4 (6.78 ± 4.24 h*ng/mL) in comparison with group 2 (12.83 ± 4.19 h*ng/mL). A significant reduction of the oral bioavailability of AFG1 was observed for group 4 (7.61 ± 4.76%) compared with group 2 (14.40 ± 4.70%), while no significant effect was observed of CP. In this experiment, no phase I nor phase II metabolites of AFG1 were observed. These findings confirm that calcination of the purified montmorillonite clay enhances the adsorption of AFG1 in the gastrointestinal tract after oral administration, thereby reducing its bioavailability, thus reducing its toxic effects.

Synthesis of novel biocomposite powder for simultaneous removal of hazardous ciprofloxacin and methylene blue: Central composite design, kinetic and isotherm studies using Brouers-Sotolongo family models.

Over the past decades, extensive efforts have been made to use biomass-based-materials for wastewater-treatment. The first purpose of this study was to develop and characterize regenerated-reed/reed-charcoal (RR-ChR), an enhanced biosorbent from Tunisian-reed (Phragmites-australis). The second aim was to assess and optimize the RR-ChR use for the removal of binary ciprofloxacin antibiotic (CIP) and methylene blue dye (MB), using Central Composite Design under Response Surface methodology. The third purpose was to explain the mechanisms involved in the biosorption-process. The study revealed that the highest removal-percentages (76.66 % for the CIP and 100 % for the MB) were obtained under optimum conditions: 1.55 g/L of adsorbent, 35 mg/L of CIP, 75 mg/L of MB, a pH of 10.42 and 115.28 min contact time. It showed that the CIP biosorption mechanism was described by Brouers-Sotolongo-fractal model, with regression-coefficient (R2) of 0.9994 and a Person's Chi-square (X2) of 0.01. The Hill kinetic model better described the MB biosorption (R2 = 1 and X2 = 1.0E-4). The isotherm studies showed that the adsorbent surface was heterogeneous and the best nonlinear-fit was obtained with the Jovanovich (R2 = 0.9711), and Brouers-Sotolongo (R2 = 0.9723) models, for the CIP and MB adsorption, respectively. Finally, the RR-ChR lignocellulosic-biocomposite-powder could be adopted as efficient and cost-effective adsorbent.

Synthesis and characterization of eco-friendly cellulose beads for copper (II) removal from aqueous solutions.

In this study, novel cellulose-bead-based biosorbents (CBBAS) were successfully synthesized from almond shell using a simple three-step process: (i) dissolution of bleached almond shell in ionic liquid (1-butyl-3-methylimidazolium chloride), (ii) coagulation of cellulose-ionic liquid solution in water and (iii) freeze-drying. Their morphological, structural and physicochemical properties were thoroughly characterized. These biomaterials exhibited a 3D-macroporous structure with interconnected pores, which provided a high number of adsorption sites. It should be noted that CBBAS biosorbents were efficiently employed for the removal of copper (II) ions from aqueous solutions, showing high adsorption capacity: 128.24 mg g-1. The biosorption equilibrium data obtained were successfully fitted to the Sips model and the kinetics were suitably described by the pseudo-second-order model. Besides, CBBAS biosorbents can be easily separated from the solution for their subsequent reuse, and thus, they represent a method for the removal of copper (II) from aqueous solutions that is not only eco-friendly but also economical.

Synthesis of cost-effective magnetic nano-biocomposites mimicking peroxidase activity for remediation of dyes.

The present study describes preparation of cellulose incorporated magnetic nano-biocomposites (CNPs) by using cellulose as base material. The prepared CNPs were characterised by SEM, EDAX, TEM, XRD, and FT-IR and found to exhibit an intrinsic peroxidase-like activity with a Km and Vmax of 550 µM and 3.8 µM/ml/min, respectively. The CNPs exhibited higher pH and thermal stability compared to commercial peroxidase. These nanocomposites were able to completely remove (i) a persistent azo dye, methyl orange at a concentration of 50 ppm, within 60 min under acidic conditions (pH 3.0) and also (ii) decolourize commercial textile dye mixture under acidic conditions within 30 min. CNP-mediated degradation of dyes into simple products was further confirmed by UV-Vis and AT-IR spectroscopy The added advantage of CNPs separation after decolourization by simple magnet due to their magnetic properties and consequent reusability makes them fairy attractive system for dye remediation from environmental samples or textile industries effluents.

Calcination Enhances the Aflatoxin and Zearalenone Binding Efficiency of a Tunisian Clay.

Clays are known to have promising adsorbing characteristics, and are used as feed additives to overcome the negative effects of mycotoxicosis in livestock farming. Modification of clay minerals by heat treatment, also called calcination, can alter their adsorption characteristics. Little information, however, is available on the effect of calcination with respect to mycotoxin binding. The purpose of this study was to characterize a Tunisian clay before and after calcination (at 550 °C), and to investigate the effectiveness of the thermal treatment of this clay on its aflatoxin B1 (AFB1), G1 (AFG1), B2 (AFB2), G2 (AFG2), and zearalenone (ZEN) adsorption capacity. Firstly, the purified clay (CP) and calcined clay (CC) were characterized with X-ray Fluorescence (XRF), X-ray Diffraction (XRD), Fourier transform infrared spectroscopy (FTIR-IR), cation exchange capacity (CEC), specific surface area (SBET), and point of zero charge (pHPZC) measurements. Secondly, an in vitro model that simulated the pH conditions of the monogastric gastrointestinal tract was used to evaluate the binding efficiency of the tested clays when artificially mixed with aflatoxins and zearalenone. The tested clay consisted mainly of smectite and illite. Purified and calcined clay had similar chemical compositions. After heat treatment, however, some changes in the mineralogical and textural properties were observed. The calcination decreased the cation exchange capacity and the specific surface, whereas the pore size was increased. Both purified and calcined clay had a binding efficacy of over 90% for AFB1 under simulated poultry GI tract conditions. Heat treatment of the clay increased the adsorption of AFB2, AFG1, and AFG2 related to the increase in pore size of the clay by the calcination process. ZEN adsorption also increased by calcination, albeit to a more stable level at pH 3 rather than at pH 7. In conclusion, calcination of clay minerals enhanced the adsorption of aflatoxins and mostly of AFG1 and AFG2 at neutral pH of the gastrointestinal tract, and thus are associated with protection against the toxic effects of aflatoxins.

Nano-Electrochemistry and Nano-Electrografting with an Original Combined AFM-SECM.

This study demonstrates the advantages of the combination between atomic force microscopy and scanning electrochemical microscopy. The combined technique can perform nano-electrochemical measurements onto agarose surface and nano-electrografting of non-conducting polymers onto conducting surfaces. This work was achieved by manufacturing an original Atomic Force Microscopy-Scanning ElectroChemical Microscopy (AFM-SECM) electrode. The capabilities of the AFM-SECM-electrode were tested with the nano-electrografting of vinylic monomers initiated by aryl diazonium salts. Nano-electrochemical and technical processes were thoroughly described, so as to allow experiments reproducing. A plausible explanation of chemical and electrochemical mechanisms, leading to the nano-grafting process, was reported. This combined technique represents the first step towards improved nano-processes for the nano-electrografting.

Localized electrografting of vinylic monomers on a conducting substrate by means of an integrated electrochemical AFM probe.

Combinations of scanning electrochemical microscopy (SECM) with other scanning probe microscopy techniques, such as atomic force microscopy (AFM), show great promise for directing localized modification, which is of great interest for chemical, biochemical and technical applications. Herein, an atomic force scanning electrochemical microscope is used as a new electrochemical lithographic tool (L-AFM-SECM) to locally electrograft, with submicrometer resolution, a non-conducting organic coating on a conducting substrate.

The in situ characterization and structuring of electrografted polyphenylene films on silicon surfaces. An AFM and XPS study.

An atomic force microscope was used so as to structure by nanofriction films of polynitrophenylene electrografted on substrates of n-type silicon (100) with the native oxide on the top of the surface. AFM measurements of thin films thickness have been carried out in the electrolytic solution for different applied potentials during the electrografting. This investigation allows (i) to determine the relationship between the applied potential and the final thickness of electrografted polyphenylene films and (ii) to specify how the thin layers grow. XPS analysis confirmed the AFM observations on (i) the effective shaving of the grafted polymer chains under mechanical stress and (ii) the existence of a potential threshold for electrografting a polyphenylene film on silicon oxide surfaces. The presence of a residual film in the rubbed zone was attributed to stronger interactions between the first electrografted layer and the native oxide of silicon (through Si-C or/and Si-O-C bonds) than those insuring the cohesion of the multilayer (C-C and C-N bonds).