The Corrosion Inhibition of Montmorillonite Nanoclay for Steel in Acidic Solution.

The aim of this research is to study the anticorrosive behavior of a coating consisting of modified montmorillonite nanoclay as an inorganic green inhibitor. The anticorrosion protection for mild steel in 1.0 M HCl solution is studied via weight loss, electrochemical methods, SEM, and XRD. The results proved that montmorillonite nanoclay acts as a good inhibitor with a mixed-type character for steel in an acidic solution. Both anodic and cathodic processes on the metal surface are slowed down. There is a clear direct correlation between the added amount of montmorillonite nanoclay and the inhibition efficiency, reaching a value of 75%. The inhibition mechanism involves the adsorption of the montmorillonite nanoclay onto the metal surface. Weight loss experiments are carried out with steel samples in 1.0 M HCl solution at room temperature, and the same trend of inhibition is produced. SEM was used to image the surface at the different stages of the corrosion inhibition process, and also to examine the starting nanoclay and steel. XRD was used to characterize the nanoparticle structure of the coating. Montmorillonite nanoclay is an environmentally friendly material that improved the corrosion resistance of mild steel in an acidic medium.

Facile Production Method of PbS Nanoparticles via Mechanical Milling of Galena Ore.

In this research, some physical properties such as the density, specific heat capacity, and micro-hardness of galena ore lumps purchased from the public market were determined. The microscopic study, using the scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS), confirmed that the as-received galena ore was mostly lead sulfide (PbS). The XRD pattern of the galena powder also elucidated that all the peaks were assigned to PbS. In addition, the as-received galena was roughly crushed, and fine-milled using a high-vibration milling machine with tungsten carbide rings. Nanoscale particles of about 90 nm were produced in a very short milling time of around 15 min. The obtained nanoscale powder was well investigated in the SEM at low and high magnifications to assess the exact range of particle size. Meanwhile, the SEM was employed to investigate the microstructure of sintered samples, where a part of the milled galena powder was compacted and sintered at 700 °C for 2 h. Again, the result of this investigation proved the formation of PbS with even smaller grain size compared with the grain size of the starting galena ore. A high relative sinter density of approximately 97% for galena powder was achieved by sintering under vacuum.

Extraction of Anthocyanins from Black Grape By-Products and Improving Their Stability Using Cobalt(II) Complexation.

This study was conducted to investigate the effect of cobalt complexation on the spectral properties of anthocyanins (AC) extracted from black grape pomace (Black Magic) and the effect of complexation on the pH stability of AC during storage. Initially, cobalt acetate tetrahydrate aqueous solution was complexed with AC crude extract and diluted separately in buffer solutions with different pH (3.5, 4.5, 5.5, and 6.5). Afterward, spectral changes were determined spectrophotometrically. pH stability was investigated using the same buffer solutions and stored for 7 days in the dark at room temperature, and the absorbance of each solution was measured daily using a spectrophotometer. Results indicated that complexation caused similar hypsochromic and hyperchromic shifts in λmax at all pH values. With regard to pH stability, the degradation of complexed AC followed first-order reaction kinetics causing half-lives to increase up to 80-fold as compared with noncomplexed AC, which was due to the sharp decrease in K (per day), indicating an improved pH stability as compared with noncomplexed AC. Therefore, Co(II) could be used in the stabilization of grape AC for the coloration of a wide range of foods and food products at near-neutral pH environments considering the health benefits of grape AC and the maximum nontoxic dose of Co(II) salt.

Characterization of Chlorhexidine-Impregnated Cellulose-Based Hydrogel Films Intended for the Treatment of Periodontitis.

Periodontitis comprises a chronic inflammation that is initiated by microbiota biofilm. If left untreated, periodontitis may lead to permanent tooth loss. Herein, we propose to design and improve a localized form of therapy comprising a chlorhexidine-impregnated hydrogel. Hydrogel films were prepared by varying the ratio between cellulose (MCC) and carboxymethylcellulose sodium (CMC) using the crosslinker epichlorohydrin (ECH). The hydrogel was loaded with chlorhexidine. Increasing the CMC ratio led to a reduction in the number of pores, an increase in their size, lower glass transition temperature (T g ), decreased Young's modulus, and increased film stretching and affected the time of release. Bacterial and fungal zones of inhibition showed similar activity and were not affected by the CMC and MCC ratio. Hydrogels loaded with chlorhexidine prevented the growth of S. oralis and C. albicans microorganisms and may provide a promising local delivery system for treating periodontitis.

Calculations of the molecular interactions in 1,3-dibromo-2,4,6-trimethyl-benzene: which methyl groups are quasi-free rotors in the crystal?

Dibromomesitylene (DBMH) is one of the few molecules in which a methyl group is a quasi-free rotor in the crystal state. Density functional theory calculations - using the Born-Oppenheimer approximation (BOa) - indicate that in isolated DBMH, Me4 and Me6 are highly hindered in a 3-fold potential V3 > 55 meV while Me2 symmetrically located between two Br atoms has a small 6-fold rotation hindering potential: V6 ∼ 8 meV. Inelastic neutron scattering studies have shown that this is also true in the crystal, the Me2 tunneling gap being 390 µeV at 4.2 K and V6 ∼ 18 meV. In the monoclinic DBMH crystal, molecules are packed in an anti-ferroelectric manner along the oblique a axis, favoring strong van der Waals interactions, while in the corrugated bc planes each molecule has a quasi hexagonal environment and weaker interactions. This results in the nearby environment of Me2 only being composed of hydrogen atoms. This explains why the Me2 rotation barrier remains small in the crystal and mainly 6-fold. Using the same potentials in the Schrödinger equation for a -CD3 rotor has allowed predicting a tunneling gap of 69 µeV for deuterated Me2 in very good agreement with inelastic neutron scattering measurements. Therefore, because of a rare and unexpected local symmetry in the crystal, the Me2 rotation barrier remains small and 6-fold and hydrogen nuclei are highly delocalized and not relevant to the Born-Oppenheimer approximation. This and the neglect of spin states explain the failure of density functional theory calculations for finding the rotation energy levels of Me2.

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+.

Characterization of TiO(2)-chitosan/glass photocatalyst for the removal of a monoazo dye via photodegradation-adsorption process.

In this paper, the newly explored TiO(2)-Chitosan/Glass was suggested as a promising alternative material to conventional means of wastewater treatment. Characterization of TiO(2)-Chitosan/Glass photocatalyst was studied with SEM-EDX, XRD, and Fourier transform infrared spectroscopy (FTIR) analysis. The combination effect of photodegradation-adsorption process for the removal of methyl orange (MO), an acid dye of the monoazo series occur promisingly when four layers of TiO(2)-Chitosan/Glass photocatalyst was used for MO removal. Approximately, 87.0% of total MO removal was achieved. The reactive -NH(2), -OH, and metal oxide contents in the prepared photocatalyst responsible for the photodegradation-adsorption effect were confirmed by FTIR study. Similarly, MO removal behavior was well supported by SEM-EDX and XRD analysis. Significant dependence of MO removal on the TiO(2)-Chitosan loading can be explained in terms of relationship between quantum yield of photocatalytic reactions and photocatalyst structure/activity. Hence, the research work done thus far suggests a new method, having both the advantages of photodegradation-adsorption process in the abatement of various wastewater pollutants.