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New Schiff base ligand: 4-methoxy salicaldhyde-2-2-phenyl-hydrazono acetaldehíyde prepared by facile method. The molecular structures characterized by elemental analysis and proton magnetic resonance spectra (1H-NMR spectra). This spectra at the chemical shifts (3.5–10.39 ppm) confirmed the types and the numbers of protons. The sharp melting point at the range 110–112 °C confirmed purity. New optically active metal (samarium, terbium and gadolinium) complexes of the Schiff base synthesized in a one pot reaction. Vibrational IR spectra confirmed functional groups. Scanning electron microscopy micrographs confirmed that the modified microstructure of the metal complexes differed in morphology than the ligand. Powder X-ray diffraction patterns confirmed good crystalline structure. The optically activity of the solid metal complexes confirmed from electronic absorption spectra. The UV absorbance band at the wavelength range 280–390 nm and the intense phosphorescence bands up to 830 nm enabled application in photo dynamic therapy for apoptosis cancer cells by conversion triplet oxygen in the tissues into reactive singlet oxygen. Low charge transfer energy: 2.59–2.61 eV, high molar extinction coefficients (ε) at the order of magnitude M− 1 cm− 1 and the intense phosphorescence bands reflected good photodynamic activity. The metal complexes are thermally stable. [ABSTRACT FROM AUTHOR]

The goal of this study is to develop a new effective guar gum-grafted acrylamide hydrogel for wastewater treatment, abbreviated as (guar gum-g-acrylamide). For the non-biodegradable and hazardous synthetic acid red 8, the produced guar gum-g-acrylamide hydrogel is a promising thermally stable adsorbent. Microwave-aided technique, ammonium persulfate initiator, and N,N′-methylene-bis-acrylamide cross-linker are used to make a hydrogel comprising natural polysaccharides guar gum grafted by poly acrylamide. Fourier transformer infrared (FTIR) spectra and scanning electron microscopy (SEM) demonstrate that varied percentages of acrylamide successfully graft the backbone of guar gum. When the grafting percentage of acrylamide is raised, the hydrogel's maximum adsorption capacity (qe) increases. At pH 1 of dye solution, maximum adsorption capacity (qe) is 18 mg.g−1, at pH 9; qe is decreased up to 8 mg.g−1. At 0.5 g.L−1 hydrogel, the dye has a low removal percentage (34%), but when the hydrogel dosage is increased to 8 g.L−1, the removal percentage increases to 90%. When the initial AR8 dye concentration was increased from 50 to 300 mg.L−1, the removal percentage reduced to 20% and the adsorbed quantity dye increased from 17 to 44 mg.g−1, but both parameters became limited above this dye concentration. Other ideal conditions for AR8 dye removal by the hydrogel include 60 min of contact time, 150 revolutions per minute (rpm), and a temperature of 20 degrees Celsius. The AR8 dye adsorption kinetic is pseudo-second order, assuming electrostatic interaction between the negatively charged AR8 dye molecules and the positively charged hydrogel-functional group. The adsorption values fit the Langmuir isotherm, with qmax. of 54.054 mg.g−1. The adsorbed quantity (qe) decreases as the temperature rises, indicating that dye molecules physisorbed on the hydrogel pores, and the maximum adsorption capacity is at 20 °C. The exothermic and spontaneity of adsorption were confirmed by the negative values of heat of adsorption (∆H°ads.) and standard Gibbs free energy of adsorption (∆G°ads.). The reusability of the hydrogel was validated after three cycles of desorption of AR8 dye from the hydrogel surface in alkaline solution. [ABSTRACT FROM AUTHOR]

Heterogeneous membranes are generally prepared by mixing ion-exchange (IE) resins, whether cation or anion resins, with a polymer matrix, in which the resin is well embedded within the polymer in a homogeneous manner. In the present paper, novel membranes were fabricated and different variables were investigated, such as types of polymer matrix whether cellulose acetate (CA) or cellulose acetate butyrate (CAB), source (properties) of CA, de-esterified membranes, type of IE resins (cationic, anionic, or nonionic), and ground or pristine resins. It was found that ground resins gave thinner membranes with better perm-selectivity for both cationic and anionic IE resins with the two brands of CA tested. The nonionic IE resin gave adverse results as expected, especially when it was pulverized before mixing with the polymers. CAB gave unfavorable results compared with the two types of CA polymers studied and gave lower perm-selectivity especially when the IE resins were ground before mixing to the CAB polymer. [ABSTRACT FROM AUTHOR]