scholarly journals Influence of pH on the Electropolymerisation of 2-Aminophenol and 2-Aminobenzyl Alcohol

2015 ◽  
Vol 18 (1) ◽  
pp. 037-041
Author(s):  
Ahmad S. Barham

The electrochemical oxidation and polymerisation of 2-aminophenol and 2-aminobenzyl alcohol in aqueous solutions of different pH values has been studied. Polymer films of the studied monomers on gold electrodes were synthesized. The behaviour of both monomers is quite different, illustrating the resonance effect of the hydroxyl group being bound directly to the benzene ring for 2-aminophenol. For each compound it is shown that oxidation in acidic solutions is most difficult due to the protonation of the amine group. These polymer films can be used for applications such as corrosion protection and as structures from which textured electrodes, microelectrode arrays for example, can be generated.

2018 ◽  
Vol 83 (2) ◽  
pp. 251-264 ◽  
Author(s):  
Sofia Sarri ◽  
Panagiotis Misaelides ◽  
Dimitrios Zamboulis ◽  
Jolanta Warchoł

The use of a polyethylenimine?epichlorohydrin resin for the boron removal from aqueous solutions (boron concentration: 100?5000 mg L-1) of non-adjusted and pre-adjusted pH (pHnat, pHinit 8.0, 9.0 and 10.0) aqueous solutions was investigated using a batch technique. The boron concentration in the solutions after sorption was determined photometrically. The results indicated that the pH-dependent boron uptake was related to the protonation/deprotonation of the surface functional groups of the resin and to the boron speciation in solutions of different pH values. The maximum boron sorption capacity observed in solutions of pH 9.0 was 55 mg g-1 exceeding the majority of other commercial or alternative sorbents. Five empirical adsorption equations (Freundlich, Langmuir, Redlich?Peterson, Langmuir?Freundlich and Toth) were applied to the modelling of the boron adsorption equilibrium. The modelling results identified the homogenous boron sorption from acidic and heterogeneous from alkaline solutions. At alkaline pH, the system non-ideality can originate either from the different binding mechanism or from the competitive sorption of different boron species. The homogenous type boron sorption from acidic solutions was further confirmed by kinetic studies


2015 ◽  
Vol 22 (1) ◽  
pp. 95-105 ◽  
Author(s):  
Krzysztof Kuśmierek ◽  
Andrzej Świątkowski

Abstract Adsorptive removal of 2-, 3- and 4-chlorophenol from aqueous solutions by granular activated carbon was studied. The influence of different experimental parameters like initial concentration, carbon dosage and pH on the adsorption of monochlorophenols were evaluated. The influence of type of acid and base used for water acidification or alkalization was also tested. The results indicate that acidic pH is favorable for the adsorption of chlorophenols; however the type of acid or alkali used for the change of pH has a little influence and did not significantly affect the adsorption efficiency. The pH played an important role in the adsorption kinetics of chlorophenols at pH values above the pKa values of the compounds, while little influence on adsorption rate was observed if pH was decreased below the pKa values


1986 ◽  
Vol 49 (5) ◽  
pp. 383-388 ◽  
Author(s):  
PETER SPORNS ◽  
SUET KWAN ◽  
LAWRENCE A. ROTH

Oxytetracycline (OTC), also known commercially as Terramycin, was determined to be more stable in honey than in buffered aqueous solutions at similar pH values and temperatures. A rapid high performance liquid chromatography (HPLC) method was developed to detect and quantitate OTC using a 1:1 dilution (wt/wt) of honey samples in water. Using 355 nm as the wavelength of detection, amounts as low as 0.5 μg/ml could be detected in the above solution. The limits of detection were lowered considerably by a double extraction procedure.


2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Sung-Wook Yun ◽  
Chan Yu

Decades of mining in South Korea have resulted in the contamination of large amounts of soil by metals. The most feasible approach to site restoration requires the use of a stabilization agent to reduce metal mobility. This study examined the leaching characteristics of limestone used as a stabilization agent when subjected to solutions of differing pH. In a laboratory-scale column test, solutions with pH values of 3.5, 4.6, and 5.6, representing acidic to nonacidic rainfall, were applied to soil mixed with limestone. Test results indicate that metal components can be released with the addition of acidic solutions, even if the soil is highly alkaline. Cd and Zn, in particular, exhibited abrupt or continuous leaching when exposed to acid solutions, indicating the potential for contamination of water systems as metal-laden soils are exposed to the slightly acidic rainfall typical of South Korea. Treatment using stabilization agents such as limestone may reduce leaching of metals from the contaminated soil. Stabilizing metal-contaminated farmland is an economical and feasible way to reduce pollutants around abandoned metal mines.


1969 ◽  
Vol 113 (4) ◽  
pp. 611-615 ◽  
Author(s):  
J. Leichter ◽  
M. A. Joslyn

Results are presented on the rate of thiamin cleavage by sulphite in aqueous solutions as affected by temperature (20–70°), pH(2·5–7·0), and variation of the concentration of either thiamin (1–20μm) or sulphite (10–5000μm as sulphur dioxide). Plots of the logarithm of percentage of residual thiamin against time were found to be linear and cleavage thus was first-order with respect to thiamin. At pH5 the rate was also found to be proportional to the sulphite concentration. In the pH region 2·5–7·0 at 25° the rate constant was 50m−1hr.−1 at pH5·5–6·0, and decreased at higher or lower pH values. The rate of reaction increased between 20° and 70°, indicating a heat of activation of 13·6kcal./mole.


2003 ◽  
Vol 38 (2) ◽  
pp. 393-411 ◽  
Author(s):  
Soufiane Tahiri ◽  
Ali Messaoudi ◽  
Abderrahman Albizane ◽  
Mohamed Azzi ◽  
Mohamed Bouhria ◽  
...  

Abstract In this work, the ability of chrome shavings and of crust leather buffing dusts to remove dyes from aqueous solutions has been studied. Buffing dusts proved to be a much better adsorbent than chrome shavings for cationic dyes. The adsorption of anionic dyes is very important on two studied wastes. The pH has an obvious influence on the adsorption of dyes. Adsorption of cationic dyes is less favourable under acidic conditions (pH <3.5) and at high pH values (pH >10.5). The adsorption of anionic dyes on both adsorbents is more favourable under acidic conditions (pH <3). The adsorption on chrome shavings is improved by the use of finer particles. The kinetic adsorption was also studied. Adsorption isotherms, at the optimum operating conditions, were determined. Adsorption follows the Langmuir model. The isotherm parameters have been calculated. The column technique could be applied to treat significant volumes of solutions.


2019 ◽  
Vol 16 (31) ◽  
pp. 755-764
Author(s):  
Roberto FERNANDEZ-MAESTRE ◽  
Alonso J MARRUGO-GONZÁLEZ

Chalcones (α,β-unsaturated ketones) containing aromatic or heterocyclic radicals are highly reactive, allowing the synthesis of novel organic compounds. In this study, the dissociation constants (pKa) of seven chalcones derived from 8-hydroxyquinoline were determined and the influence on dissociation of substituents in the phenyl group (-CH3, -OCH3, -N(CH3)2, -Cl, -Br, and -NO2) was analysed. pKa values are important because they determine the pH at which ligands are fully deprotonated -when they show their maximum chelating properties- and determine the ligands interactions at different pH values. The chalcones’ pKa’s were calculated by visible ultraviolet spectroscopy in a water-ethanol (1:1) mixture using the Henderson-Hasselbach equation. It was shown that the 8-hydroxyquinolinic fragment has a large electron donor effect on the π system of the chalcones. The introduction of substituents (R) in the phenyl fragment of the chalcones slightly affected the dissociation of the hydroxyl group and the protonation of the nitrogen in the hydroxyquinoline fragment. The acceptor substituents (Cl, Br, NO2) increased the polarity of OH- and its acidity. Nitrogen protonation decreased electron donor properties of this fragment, and deprotonation of the hydroxyl caused the opposite effect. Substituents introduction in the phenyl fragment slightly affected hydroxyl group dissociation and nitrogen protonation.


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