Removal of phenolic compounds from aqueous solution using MgCl2-impregnated activated carbons derived from olive husk: the effect of chemical structures.

Activated carbon (BC) prepared from olive oil solid waste (olive husk) by slow pyrolysis was chemically activated using MgCl2 (BC-MgCl2). The BC and BC-MgCl2 were used as adsorbents for removal of three phenolic compounds, namely, phenol (P), p-methoxyphenol (PMP) and p-nitrophenol (PNP), from aqueous solution. The uptake of these three phenolic compounds by the BC and BC-MgCl2 was better expressed by the Langmuir and Dubinin-Radushkevich (D-R) isotherm models than by the Freundlich isotherm, and the kinetics of the adsorption process followed the pseudo-second order kinetic model. The maximum monolayer adsorption capacity of P, PMP and PNP were increased from 24.938, 45.455 and 61.728 on BC to 43.860, 98.039 and 121.951 mg/g on BC-MgCl2 by factors of 1.76, 2.16 and 1.98, respectively. Therefore, the chemical activation of BC by MgCl2 is indeed of importance for improving its adsorption performances. For both adsorbents, the adsorption phenomenon for different substituted phenols is a strong function of solubility, polarity, molecule structure, and size. At the tested temperatures (25, 35 and 45 °C), the negative values of ΔG° and positive values of ΔH° and ΔS° for the adsorption of P, PMP and PNP on BC and BC-MgCl2 demonstrated that the adsorption was a spontaneous, endothermic and entropy-increasing process.

Comparison of Jordanian and standard diatomaceous earth as an adsorbent for removal of Sm(III) and Nd(III) from aqueous solution.

In this study, Jordanian diatomaceous earth (JDA) and commercial diatomaceous earth (standard diatomaceous earth, SDA) were used for adsorption of samarium (Sm)(III) and neodymium (Nd)(III) ions from aqueous solutions using batch technique as a function of initial concentration of metal ions, adsorbent dosage, ionic strength, initial pH solution, contact time, and temperature. Both adsorbents were characterized by Fourier transform infrared (FTIR), X-ray fluorescence (XRF), X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer-Emmett-Teller surface area, and cation exchange capacity (CEC). Maximum metal ion uptake was observed after 100 min of agitation, and the uptake has decreased with increasing temperature and reached a maximum at pH ≈ 5. Different types of adsorption isotherms and kinetic models were used to describe the Nd(III) and Sm(III) ion adsorption. The experimental data fitted within the following isotherms in the order Langmuir > Dubinin-Radushkevich (DR) > Freundlich and the pseudo-second-order kinetic model based on their coefficient of determination (R2), chi-square (χ2), and error function (Ferror%) values. Maximum adsorption uptakes, according to the Langmuir model, were obtained as 188.679 mg/g and 185.185 mg/g for Sm(III) and 169.492 mg/g and 149.254 mg/g for Nd(III) by JDA and SDA, respectively. The results of thermodynamic parameters showed that the adsorption of Sm(III) and Nd(III) ions onto JDA and SDA is a feasible, spontaneous, exothermic, and entropy driven. The best recovery for Sm(III) and Nd(III) was obtained when the 0.05 M EDTA + 0.05 M H3PO4 mixture was used as an eluent.

Hypolipidemic effect of novel 2,5-bis(4-hydroxybenzylidenamino)-1,3,4-thiadiazole as potential peroxisome proliferation-activated receptor-α agonist in acute hyperlipidemic rat model.

The development of new antihyperlipidemic agents with higher potency and lower side effects is of high priority. In this study, 1,3,4 thiadiazole Schiff base derivatives were synthesized as potential peroxisome proliferation-activated receptor-α (PPARα) agonists and characterized using elemental analysis, FTIR, 1H-NMR, 13C-NMR and mass spectroscopy and then tested for their hypolipidemic activity in Triton WR-1339-induced acute hyperlipidemic rat model in comparison with bezafibrate. The compounds showed significant hypolipidemic activity. Induced fit docking showed that the compounds are potential activators of PPARα with binding scores - 8.00 Kcal/mol for 2,5-bis(4-hydroxybenzylidenamino)-1,3,4-thiadiazole. PCR array analysis showed an increase in the expression of several genes involved in lipid metabolism through mitochondrial fatty acid ß oxidation and are part of PPARα signaling pathway including Acsm3, Fabp4 and Hmgcs1. Gene expression of Lrp12 and Lrp1b involved in LDL uptake by liver cells and Cyp7a1 involved in cholesterol catabolism were also found to be upregulated.

Phenol adsorption on biochar prepared from the pine fruit shells: Equilibrium, kinetic and thermodynamics studies.

Biochar samples were prepared from pine fruit shell (PFS) biomass using slow pyrolysis for 1 h at three different temperatures (350, 450 and 550°C). Batch experiments were carried out for the biosorption of phenol onto these biochars. The effect of biosorption experimental parameters such as adsorbent dosage, ionic strength, initial solution pH, contact time and temperatures has been investigated. Experimental equilibrium data were fitted to Langmuir, Freundlich, and Dubinin-Radushkevich (D-R) isotherms by non-linear regression method. The experimental kinetic data were also fitted to Lagergren pseudo-first order, pseudo-second order, Elovich and intraparticle diffusion models by non-linear regression method. Determination coefficient (R2), chi-squared (χ2) and error function (Ferror%) were used to determine the optimum isotherm and kinetic by non-linear regression method. Kinetics results were best described by pseudo-second order model for phenol onto three biochars. Thermodynamic parameters were estimated and implied that the adsorption process is spontaneous and exothermic in nature.

Conducting cellulose/TiO2 composites by in situ polymerization of pyrrole.

Cellulose/polypyrrole and cellulose/polypyrrole-TiO2 composites were prepared via in situ oxidative chemical polymerization of pyrrole using FeCl3 as oxidant. The concentration effect of pyrrole on the structure and properties of prepared matrix has been investigated. Furthermore, the structure of the prepared materials was characterized using Fourier transform infrared spectroscopy (FTIR), Scanning electron microscopy (SEM), X-ray Diffraction (XRD), and Thermal gravimetrical analysis (TGA). The results exhibited that the addition of cellulose and TiO2 increase the thermal stability of the polypyrrole system. Moreover, dielectric properties of the obtained composites were studied over frequency range from 42Hz to 5MHz. The electrical measurements including dielectric constant, ε'(ω), dielectric loss, ε''(ω), loss tangent, tan δ and ac conductivity, σac were carried.

Characterization of biochar prepared from slow pyrolysis of Jordanian olive oil processing solid waste and adsorption efficiency of Hg2+ ions in aqueous solutions.

Solid waste from Jordanian olive oil processing (OOSW) was used to prepare biochar samples by slow pyrolysis at terminal temperatures of 350, 450, 550 and 630 °C; henceforth known as BC-350, BC-450, BC-550 and BC-630, respectively. These samples were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy and X-ray diffraction, ash content, moisture content and surface area. The ability of the biochar to remove Hg2+ ions from aqueous solutions was investigated in laboratory scale batch experiments. The kinetics, effect of pH and temperature were studied. The optimum pH value for Hg2+ adsorption was 5. Dubinin-Radushkevich (D-R) isotherm model was the best fit for the experimental results. Based on the D-R model, the maximum adsorption capacities at 25 °C were 84.93, 94.48, 96.11 and 104.59 mg.g-1, for BC-350, BC-450, BC-550 and BC-630, respectively. The pseudo-second-order kinetic model was a good fit for the experimental data. The calculated change in free energy ΔG and enthalpy ΔH indicated that the adsorption process was spontaneous and exothermic in nature. The positive value of ΔS showed increased randomness of the solid/solution interface during the adsorption. The results indicated that biochar derived from OOSW can be a good adsorbent for treatment of water contaminated with Hg2+.

The removal of phenol from aqueous solutions by adsorption using surfactant-modified bentonite and kaolinite.

The natural bentonite (BC) and kaolinite (KC) were modified with two surfactant of hexadecyltrimethylammonium bromide (HDTMA) and phenyltrimethylammonium bromide (PTMA) to form four kinds of organic-modified clays, i.e., HDTMA-bentonite (BHM), HDTMA-kaolinite (KHM), PTMA-bentonite (KPM) and PTMA-kaolinite (KPM). The modified minerals were characterized by X-ray fluorescence (XRF), X-ray diffraction (XRD) and FT-IR spectroscopy. The surface areas were determined using methylene blue adsorption method. Cation-exchange capacity (CEC) was estimated using an ethylenediamine complex of copper method and the modifier loading was calculated from the total carbon analysis. The ability of raw and organo-modified clays to remove phenol from aqueous solutions has been carried out as a function of contact time, pH and temperatures using a batch technique. The removal of phenol from aqueous solutions by modified clays seems to be more effective than unmodified samples. The adsorption capacity was found to increase with increasing temperature indication that the adsorptions were endothermic. The adsorption of phenol onto these clays was found to be increased by increasing of pH value and the adsorption patterns data are correlated well by Langmuir and Freundlich isotherm models and that the adsorption is physical in nature. The experimental data fitted very well with the pseudo-second-order kinetic model. The thermodynamic study of adsorption process showed that the adsorption of phenol with these six adsorbents was carried out spontaneously, and the process was endothermic in nature.