Preparation and Characterization of a New Polymeric Multi-Layered Material Based K-Carrageenan and Alginate for Efficient Bio-Sorption of Methylene Blue Dye

The current study highlights a novel bio-sorbent design based on polyelectrolyte multi-layers (PEM) biopolymeric material. First layer was composed of sodium alginate and the second was constituted of citric acid and k-carrageenan. The PEM system was crosslinked to non-woven cellulosic textile material. Resulting materials were characterized using FT-IR, SEM, and thermal analysis (TGA and DTA). FT-IR analysis confirmed chemical interconnection of PEM bio-sorbent system. SEM features indicated that the microspaces between fibers were filled with layers of functionalizing polymers. PEM exhibited higher surface roughness compared to virgin sample. This modification of the surface morphology confirmed the stability and the effectiveness of the grafting method. Virgin cellulosic sample decomposed at 370 °C. However, PEM samples decomposed at 250 °C and 370 °C, which were attributed to the thermal decomposition of crosslinked sodium alginate and k-carrageenan and cellulose, respectively. The bio-sorbent performances were evaluated under different experimental conditions including pH, time, temperature, and initial dye concentration. The maximum adsorbed amounts of methylene blue are 124.4 mg/g and 522.4 mg/g for the untreated and grafted materials, respectively. The improvement in dye sorption evidenced the grafting of carboxylate and sulfonate groups onto cellulose surface. Adsorption process complied well with pseudo-first-order and Langmuir equations

Preparation and Characterization of a New Polymeric Multi-Layered Material Based K-Carrageenan and Alginate for Efficient Bio-Sorption of Methylene Blue Dye

The current study highlights a novel bio-sorbent design based on polyelectrolyte multi-layers (PEM) biopolymeric material. First layer was composed of sodium alginate and the second was constituted of citric acid and k-carrageenan. The PEM system was crosslinked to non-woven cellulosic textile material. Resulting materials were characterized using FT-IR, SEM, and thermal analysis (TGA and DTA). FT-IR analysis confirmed chemical interconnection of PEM bio-sorbent system. SEM features indicated that the microspaces between fibers were filled with layers of functionalizing polymers. PEM exhibited higher surface roughness compared to virgin sample. This modification of the surface morphology confirmed the stability and the effectiveness of the grafting method. Virgin cellulosic sample decomposed at 370 °C. However, PEM samples decomposed at 250 °C and 370 °C, which were attributed to the thermal decomposition of crosslinked sodium alginate and k-carrageenan and cellulose, respectively. The bio-sorbent performances were evaluated under different experimental conditions including pH, time, temperature, and initial dye concentration. The maximum adsorbed amounts of methylene blue are 124.4 mg/g and 522.4 mg/g for the untreated and grafted materials, respectively. The improvement in dye sorption evidenced the grafting of carboxylate and sulfonate groups onto cellulose surface. Adsorption process complied well with pseudo-first-order and Langmuir equations

Bioactive composites of hydroxyapatite/polyvinylpyrrolidone for bone regeneration applications

<p>The implantation of bioactive composites for bone repair applications has recently gained the attention of many research groups. The present paper introduces a method for grafting of polyvinylpyrrolidone on the surface of hydroxyapatite (CaHAp) microcrystals by wet precipitation method to manufacture new composite scaffolds with suitability for bone tissue engineering. After grafting with the polymer, the degree of CaHAp crystallinity decreased, and its thermal behavior changed indicating a strong interaction between them. Homogenous clusters of CaHAp particles within the polymeric matrix were observed in combination with an increase in the roughness of the resulting structures. Bioactivity of the composites was tested using MTT assay; a higher viability of the seeded cells was observed relative to those cultured with CaHAp powder.</p

Characterization of Raw and Treated Calotropis Gigantea Fibers: Application to the Adsorption of Methylene Blue Dye

The present paper focuses on the valorization of raw and treated Calotropis gigantea fibers as a natural and low-cost biosorbent for methylene blue. To assess the effect of the fiber treatment, chemical, morphological, thermal, and structural characterizations were performed. The adsorption characteristics were achieved by varying the pH, the initial dye concentrations, temperature, and contact time. The pseudo-first-order kinetic model fits accurately the experimental data. The adsorption isotherms have been fitted using several models. The monolayer model with one energy is finally adopted because the error on the parameters inherent to the model is relatively small. The adsorption isotherms of the raw and treated fibers reveal that when the temperature increases, the adsorption capacity is reduced. The maximum adsorption capacity is obtained at the temperature 25°C. It is equal to 31 mg/g and 13 mg/g for the raw fiber and the treated fiber, respectively. The steric parameter $$n$$ is greater than one for the raw fiber, whereas it is smaller than one for the treated fiber. The adsorption energy is about 19 kJ/mol. The Calotropis gigantea fiber seems to be a potential candidate for the removal of methylene blue from polluted water

A combined experimental and theoretical study on the synthesis, spectroscopic characterization of Magnesium(II) porphyrin complex with DMAP axial ligand and antifungal activity

International audienceWe report in the present paper the synthesis, the spectroscopic, structural, and electrochemical properties of a new magnesium(II) coordination compound namely the bis(4-dimethylaminopyridine)[meso-tetra(p-tolyl)porphyrinato)]magnesium(II) dichloromethane disolvate complex with the formula [Mg(TTP)(DMAP)2]•2CH2Cl2 (I). This species crystallizes in the triclinic crystal system with the centrosymmetric space group P-1. The crystal lattice of (I) is stabilized by C__H…Cg (Cg is the centroid of a phenyl ring) and C__H…Cl intermolecular interactions. Further insights on these weak intermolecular contacts are provided by the Hirshfeld surface analysis. This new Mg(II) porphyrin species was characterized by 1H NMR, IR, fluorescence, UV/Vis spectroscopy and ESI-HRMS mass spectrometry. A cyclic voltammetry investigation of this new metalloporphyrin was also reported. Furthermore, the bioactivity of the H2TTP free base porphyrin, the [Mg(TTP)] starting material and [Mg(TTP)(DMAP)2]•2CH2Cl2 (I) was evaluated in vitro, by examining their inhibitory effect against three strains of Candida viz. C. albicans, C. glabrata and C. tropicalis with MIC values in the range 2.5 to 10 μg.mL−1. The screening of the susceptibility of M. canis and T. rubrum clinical strains on the three porphyrinic derivatives is also reported

Electrochemical sensor based on gum Arabic nanoparticles for rapid and in-situ detection of different heavy metals in real samples

The key solution to combat trace metal pollution and keep the environment, ecosystem, animals, and humans safe is earlier and rapid trace metal detection. For all these reasons, we propose in this work the design of a simple electrochemical sensor functionalized with green nanoparticles for electrochemical detection of the fourth most dangerous heavy metal ions namely copper, zinc, lead, and mercury. The green nanoparticles are fabricated by a one-step, consisting of reducing platinum nanoparticles by a natural gum Arabic polymer. To guarantee the success of these nanoparticles' design, the nanoparticles have been characterized by Fourier-transform infrared spectroscopy FTIR, and thermogravimetric TGA techniques. While, for the electrochemical characterization, we have adopted cyclic voltammetry CV and electrochemical impedance spectroscopy EIS to control different steps of surface modification, and the differential pulse anodic stripping DPAS was monitored to follow up the electrochemical detection of different heavy metals. Results: have confirmed the good chemical and physical properties of the elaborated nanoparticles. As, the developed sensor showed a specific electrochemical response toward the heavy metal ions separately, with a lower limit of detection lower LOD than that recommended by the World Health Organization, in order of 9.6 ppb for Cu2+, 1.9 ppb for Zn2+, 0.9 ppb for Hg2+, and 4.2 ppb for Pb2+. Impressively, the elaborated sensor has demonstrated also high stability, outstanding sensitivity, and excellent analytical performance.In addition, the elaborated analytical tool has been successfully applied to the determination of various heavy metal ions in real samples, reflecting then its promising prospect in practical application