In-situ magnetic alginate coated chitosan core@shell beads with excellent performance in simulated and real wastewater treatment: Behavior, mechanisms, and new perspectives.

Herein, a new hybrid magnetic core@shell biocomposite was prepared based on an alginate-bentonite core and a chitosan shell layer (mAB@Cs) where magnetic Fe3O4 NPs (50.7 nm) were in-situ generated on the surface via a simple non-thermal co-precipitation approach. The biocomposite has a high ability to magnetically separate and remove organic (ciprofloxacin (CPX)) and seven toxic inorganic (Cu2+, Cd2+, Co2+, Ni2+, Pb2+, Zn2+, and Hg2+) contaminants from simulated wastewater. Experimental results showed a CPX monolayer chemisorption with a Langmuir maximum adsorption capacity of 264.7 mg/g, maintained effectiveness up to the fifth cycle, and high removal rates of heavy metals ranging from 74.89 % to 99.86 % corresponding to adsorption capacities ranging from 12 to 20 mg/g. For a more accurate evaluation, the biocomposite was tested on a real urban wastewater sample (RWW) and it has manifested a noteworthy efficiency in removing a mixture of inorganic pollutants in terms of potassium K+ and orthophosphate phosphorous P-PO43-, and organic matter in terms of biological oxygen demand (BOD) and chemical oxygen demand (COD) with 46 %, 90 %, 84 %, and 64 % removal efficiencies, respectively. On top of this, a high inactivation rate of E. coli of the order of 96 % was recorded, making the prepared magnetic biocomposite adept for the simultaneous removal of emergent wastewater pollutants, from organic, inorganic, to pathogen microorganisms.

Porous polyvinyl fluoride coated cellulose beads for efficient removal of Cd(II) from phosphoric acid.

In order to enhance the removal of cadmium from phosphoric acid, it is imperative to explore novel resources that may be utilized for the development of highly effective and environmentally sustainable adsorbents. Cellulose beads are composed of naturally occurring polysaccharide fibers and find extensive utilization across several industrial sectors and applications. Within this framework, this research paper presents a green and simple method for producing porous cellulose beads using date palm fibers as the preferred raw material. The innovation lies in immersing the obtained cellulose beads in a Polyvinyl fluoride (PVDF)/N,N-dimethylformamide (DMF) suspension as a coating polymer with different concentrations (2.5, 5, 10 %) to maintain their stability in an acidic environment. The surface of cellulose/PVDF beads were subjected to multiple characterizations like Fourier transform infrared (FTIR) spectroscopy, Scanning electron microscopy (SEM), Thermogravimetric analysis (TGA), size distribution then pH stability confirming that the coating has been perfectly achieved and conserved well the shape of the beads. The coated cellulose/PVDF-2.5 % underwent evaluation by the process of batch adsorption experiments while different parameters were varied including contact time (5, 10, 20, 30, 60, 90 min), temperature (25, 35, 45 and 55 °C), and adsorbent mass (20, 40, 60, 80 and 100 mg). The obtained ICP data showed that the adsorption rate of Cd (II) from phosphoric acid medium decreased while increasing both temperature from 25 to 55 °C and contact time from 5 to 90 min while adding more adsorbent dosage from 20 to 100 mg enhanced the removal percentage. The cellulose/PVDF-2.5 % was more effective with an adsorption capacity equal to 3.4998 mg/g at optimal conditions including 25 °C as the temperature after 5 min as contact time and by adding a mass 100 mg of the biosorbent while the pH = 2 of the solution is maintained the same. The examined material's adsorption processes proved to be exothermic and non-spontaneous, and it proved that the pseudo-second-order model provided the best match for the cellulose/PVDF-2.5 % beads kinetics data. Furthermore, the cellulose beads exhibited exceptional reusability for up to four repeated cycles without undergoing desorption. The present study offers a viable approach for producing environmentally sustainable biomass-derived adsorbents. Additionally, the study validates the potential of cellulose/PVDF beads as an intriguing material for phosphoric acid decadmiation.

Cellulose beads supported CoFe2O4: A novel heterogeneous catalyst for efficient rhodamine B degradation via advanced oxidation processes.

In this study, a novel mechanical process was used to produce cellulose beads (CB). These beads were then doped with cobalt ferrite nanoparticles (CoFe2O4 NPs) to serve as catalysts for the degradation of rhodamine B (RhB) through peroxymonosulfate (PMS) activation. The physical and chemical properties of CoFe2O4 and CoFe2O4@CB catalysts were characterized using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) combined with energy dispersive X-ray spectrometer (EDX), scanning transmission electron microscopy (STEM) techniques, and thermogravimetric analysis (TGA). To optimize RhB degradation efficiency, Response Surface Methodology (RSM) was employed, utilizing the Box-Behnken design (BBD). Under the optimized conditions of a catalyst dosage of 0.40 g/L, PMS dosage of 0.98 mM, RhB concentration of 40 mg/L, pH of 5.27, and reaction time of 60 min, a remarkable degradation efficiency of 98.51 % was achieved at a temperature of 25 °C. In quenching experiments, 1O2, SO4•-, and HO• species are produced in the CoFe2O4@CB/PMS system, with 1O2, and SO4•- species dominating RhB degradation. Remarkably, the new CoFe2O4@CB catalyst has demonstrated exceptional stability and reusability, validated by recycling tests (up to 78 % of RhB degradation efficiency after a 5-cycle experiment) and subsequent characterizations (FTIR, SEM, and EDX) emphasizing unchanged bands, uniform distribution, and consistent composition after reuse cycles. These results demonstrate the effectiveness of mechanically produced CoFe2O4@CB catalysts for advanced oxidation processes (AOPs), with promising applications in wastewater treatment.

Hemp cellulose nanocrystals for functional chitosan/polyvinyl alcohol-based films for food packaging applications.

Hemp is known for its swift growth and remarkable sustainability, requiring significantly less water, an adaptable cultivation to a wide range of climates when compared to other fibers sources, making it a practical and environmentally friendly choice for packaging materials. The current research seeks to extract cellulose nanocrystals (CNCs) from hemp fibers using alkali treatment followed by acid hydrolysis and assess their reinforcing capacity in polyvinyl alcohol (PVA) and chitosan (CS) films. AFM analysis confirmed the existence of elongated, uniquely nanosized CNC fibers. The length of the isolated CNCs was approximately 277.76 ± 61 nm, diameter was 6.38 ± 1.27 nm and its aspect ratio was 44.69 ± 11.08. The FTIR and SEM analysis indicated the successful removal of non-cellulosic compounds. Furthermore, the study explored the impact of adding CNCs at varying weight percentages (0, 0.5, 1, 2.5, and 5 wt%) as a strengthening agent on the chemical composition, structure, tensile characteristics, transparency, and water solubility of the bionanocomposite films. Adding CNCs to the CS/PVA film, up to 5 wt%, resulted in an improvement in both the Young's modulus and tensile strength of the bionanocomposite film, which are measured at (412.46 ± 10.49 MPa) and (18.60 ± 3.42 MPa), respectively, in contrast to the control films with values of (202.32 ± 22.50 MPa) and (13.72 ± 2.61 MPa), respectively. The scanning electron microscopy (SEM) images reveal the creation of a CS/PVA/CNC film that appears smooth, with no signs of clumping or clustering. The blending and introduction of CNCs have yielded transparent and biodegradable CS/PVA films. This incorporation has led to a reduction in the gas transmission rate (from 7.013 to 4.159 cm3 (m2 day·0.1 MPa))-1, a decrease in transparency (from 90.23% to 82.47%), and a lowered water solubility (from 48% to 33%). This study is the inaugural effort to propose the utilization of hemp-derived CNC as a strengthening component in the development of mechanically robust and transparent CS/PVA-CNC bio-nanocomposite films, holding substantial potential for application in the field of food packaging.

Emerging advances of composite membranes for seawater pre-treatment: a review.

As the population continues to grow, the preservation of the world's water resources is becoming a serious challenge. The seawater desalination process is considered a sustainable option for the future. The two most common technologies used in desalination are reverse osmosis (RO) and membrane distillation (MD). However, membrane fouling caused by the accumulation of contaminants on the membrane surface is an emerging and growing problem. A pre-treatment stage is required to reach optimal efficiency during the desalination process since this stage is crucial for a successful desalination process. In this regard, the development of new material-based composite membranes has the potential to upgrade the anti-fouling features of RO membranes thereby enhancing desalination efficiency due to their high permeability, hydrophilicity, selectivity mechanical strength, thermal stability, and anti-bacterial properties. The objective of this review is to present various techniques for seawater pre-treatment. The results of the use of several membrane types and methods of modification have also been discussed. The performance of composite membranes for seawater pre-treatment is defined and the future perspectives have been highlighted.

Recent progress on Ag/TiO2 photocatalysts: photocatalytic and bactericidal behaviors.

For many decades, titanium dioxide (TiO2) semiconductor has been extensively applied in several environmental applications due to its higher photocatalytic performances toward different organic pollutants, pharmaceutical compounds, and bacteria. However, its shortfall response to visible light, and the expeditious recombination rate of the photogenerated electron-hole pairs, hampers its utilization. Doping TiO2 semiconductor with silver nanoparticles is a sound strategy to (1) extend its photocatalytic activity to visible light, (2) prevent the electron/holes pairs recombination due to the formation of the Schottky barrier at the interfaces with TiO2 that act as an electron-trapping center, and (3) enhance its bactericide performances. This review focuses on the recent progress on silver-doped titanium dioxide (Ag/TiO2)-based photocatalysts. It addresses a wide range of Ag/TiO2 synthesis techniques, their physicochemical properties and discusses thoroughly the important role of silver (Ag) nanoparticles in enhancing the removal capacity and antibacterial performances of the Ag/TiO2 photocatalysts.

Efficient hybrid bionanocomposites based on iron-modified TiO2 for dye degradation via an adsorption-photocatalysis synergy under UV-Visible irradiations.

To overcome the titanium oxide limitations, Fe2O3- and Fe3O4-modified TiO2 (3:1) nanoparticles were synthesized by a humid and solid path, respectively. These nanoparticles were embedded in sodium alginate biopolymer to prepare beads with efficient adsorption and photocatalytic behaviors in cationic dye degradation under both UV and visible irradiations. Operating conditions were investigated such as initial methylene blue (MB) concentration and contact time to evaluate their impact on the process. The bead recycling was also scrutinized. We have come to the conclusion that Fe2O3-modified TiO2-Alg displayed superiorities, including expanded responsive wavelength range in the visible region (up to 700 nm), narrower band gap (1.79 eV), and better efficiency for MB removal in terms of adsorption capacities and photocatalytic effectiveness under both UV and visible irradiations. Furthermore, these beads can be effortlessly recovered from the reaction medium after the photocatalytic process and reused up to 5 cycles without any noteworthy decline in their initial properties.

Effect of iron doped titanium oxide encapsulated in alginate on photocatalytic activity for the removal of dye pollutants.

The focal point of this work is the design and comparison of two types of iron doped TiO2 prepared by a simple sol-gel method and then encapsulated in an alginate matrix. The as-prepared recyclable bio-nanocomposite photocatalysts were made of different amounts of TiO2-Fe2O3 and TiO2-Fe3O4 (1%, 2.5%, 5%, and 10%) and were developed to improve the photocatalytic efficiency of TiO2 and simultaneously to achieve an expanded visible-light response range with high visible-light absorption potential in order to degrade organic pollutants from aqueous solutions, as a potential application. As it is essential to characterize a material to better understand it, accurate characterization of the resulting bio-nanocomposites was carried out using X-ray diffraction (XRD), scanning electron microscopy coupled to energy dispersive X-ray spectroscopy (SEM-EDX), Fourier transform infrared spectroscopy (FTIR) and UV-diffuse reflectance spectroscopy (UV-DRS). In this study, the emphasis on blending the alginate and the iron doped-TiO2 photocatalyst nanoparticles results in a multicomponent particular shaped system that exhibits a porous structure, an exceptional surface area and a smaller band gap due to the presence of iron nanoparticles that could also maintain e-/hole separation for better photocatalytic activity under visible light.

Surface chemistry effects on the performance of an electrochemical DNA sensor.

E-DNA sensors are a reagentless, electrochemical oligonucleotide sensing platform based on a redox-tag modified, electrode-bound probe DNA. Because E-DNA signaling is linked to hybridization-linked changes in the dynamics of this probe, sensor performance is likely dependent on the nature of the self-assembled monolayer coating the electrode. We have investigated this question by characterizing the gain, specificity, response time and shelf-life of E-DNA sensors fabricated using a range of co-adsorbates, including both charged and neutral alkane thiols. We find that, among the thiols tested, the positively charged cysteamine gives rise to the largest and most rapid response to target and leads to significantly improved storage stability. The best mismatch specificity, however, is achieved with mercaptoethanesulfonic and mercaptoundecanol, presumably due to the destabilizing effects of, respectively, the negative charge and steric bulk of these co-adsorbates. These results demonstrate that a careful choice of co-adsorbate chemistry can lead to significant improvements in the performance of this broad class of electrochemical DNA sensors.