Plant extracts are excellent alternatives as corrosion inhibitors because of availability, low toxicity, biodegradability and low cost. In this study, corrosion tests were performed on mild steel to evaluate the effect of concentration of inhibitor, varying immersion period and temperature on the corrosion inhibition properties of Clivia nobilis leaves extract. This was done in H2SO4 and HCl acid solutions using weight loss and gasometric methods. From the weight loss results, corrosion rate and degree of surface coverage were evaluated and plotted as a function of inhibitor concentration at various immersion times. The volume of the cathodic hydrogen gas evolved was also plotted as a function of inhibitor concentration. The efficiency of inhibition in H2SO4 and HCl solutions were also compared. It was observed that corrosion inhibition efficiency increased with increasing concentration of Clivia nobilis leaf extract but not with prolonged immersion period. Experimental data obtained at 313 and 333K fitted the Freundlich and Langmuir isotherms, suggesting adsorption of Clivia nobilis leaves extract on the metal surface. Activation energy data described the interaction as electrostatic.
Densities of binary mixtures of 2-methoxyethanol (2-MeO-EtOH) and 2-ethoxyethanol (2-EtO-EtOH) with hexylamine (HLA), diethylamine (DEA), triethylamine (TEA), tert-butylamine (TBA), aniline (ANL), and benzylamine (BLA) have been determined at varying compositions of the alkoxyalkanols at 298.15 K. The excess molar volumes, VE, of the binary mixtures were calculated from the experimental density data of the mixtures and the component single solvents. The calculated excess molar volumes were fitted into the Redlich-Kister polynomial to obtain the fitting coefficients and standard deviations. The excess molar volumes of the binary mixtures of all the solvent systems investigated were negative over the entire range of the solvents composition. The negative values were attributed to stronger hydrogen bond formations between the unlike molecules of mixtures than those between the like molecules of the pure components. The magnitude of the excess molar volumes of the binary mixtures of 2-methoxyethanol and the aliphatic amines were in the order TBA > TEA > DEA > HEA. For the two aromatic amines, the magnitudes were in the order BLA > ANL. For binary mixtures of the amines and 2-ethoxyethanol, the magnitudes were in the order DEA > TEA > TBA > HEA at compositions where the mole fraction of 2-EtO-EtOH was ≤0.5 and TBA > TEA > DEA > HEA above 0.5 mole fraction of 2-EtO-EtOH.
Sedimentation data of bioactive materials are essential in formulation of suspension with desirable requirements. Batch-wise precipitation and sedimentation tests were conducted to evaluate the effect of sodium carboxymethylcellulose (Na-CMC) biopolymer solution on the sedimentation properties (rate and compaction) of trimagnesium phosphate (TMP), tricalcium phosphate (TCP) and tristrontium phosphate (TSP) precipitates. Fixed volume (1ml) of different concentrations (200ppm -2000ppm) of Na-CMC solution was mixed with fixed volume (50ml) of 0.5M, 0.05M Na3PO4 solutions. Accordingly, the resulting solutions were separately mixed with fixed volumes (50ml) of 0.5M Mg (NO3)2, 0.05M CaCL2 and 0.05M SrCL2 solutions and settling of the precipitates formed monitored. The results showed that whereas for TCP, Na-CMC exhibited a curvilinear relationship with precipitate sedimentation, non-linear relationships were observed for TMP and TSP precipitates. Between 200ppm and 2000ppm of Na-CMC addition, sedimentation rate and compaction of TCP precipitate increased by 187% and 18.5%, whereas for TMP and TSP precipitates, they increased by only (19.89% and 1%) and (30% and 0%), respectively. The results suggest that Na-CMC biopolymer is not the preferred suspending medium for suspension formulations containing TCP. For TMP and TSP precipitates, further study is needed in the light of the fact that magnesium and strontium resemble calcium.
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