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Abstract The corrosion is a great problem, which faced the world, we can not hide this problem from our live but we can reduce it by several methods as the environment need. This work discusses the corrosion inhibition of carbon steel in 1 M HCl solution by Cationic surfactants This work contains three chapters:- Chapter 1: ”Introduction” Which including that:- An introduction about surfactant (definition, classification and applications), An introduction about corrosion (definition, forms and inhibition), A literature survey on the previous studies on corrosion inhibition of carbon steel in aqueous solution is given. Chapter 2: ”Materials and experimental techniques” The experimental part includes complete description of synthesis of inhibitors used, preparation of solution, carbon steel electrode pretreatment, electrolytic cell working procedures, weight loss measurements. Chapter3: “Results and discussion” This chapter included the following parts:- 1-Preparation of surfactants The target compounds were prepared through two steps. In the first step, the ester compounds were synthesized by reaction of triethanol amine and different fatty acids (dodecanoic acid, tetradecanoic acid and hexadecanoic acid), the molar ratio is 1:1, the reaction carry out in presence of xylene as solvent and p-toluene sulfonic acid as dehydrating agent, the product is (2-hydroxyethyl)amino)ethyl alkyl ester. The reaction was completed when the water was removed from reaction system and its concentration was 1 mol. The reaction mixture was distilled under vacuum to remove the solvent. In the second step, the end products were prepared by a reaction of hexadecyl bromide with appropriate amount of 2-(bis(2- hydroxyethyl)amino)ethyl alkyl ester in the molar ratio of 1:1 to produce 2-(alkylcarbonyloxy)ethyl)hexadecyl-bis(2-hydroxy-ethyl)ammonium; bromide .The reactants were allowed to reflux in ethanol for 12 h. Then the reaction mixture was left to cool to room temperature. 2- Characterization of the synthesized surfactants The chemical structures of the prepared surfactants were confirmed by the FTIR and 1HNMR spectra. All prepared compounds have the same signals. The only difference between the signals of these compounds is the signal intensity of methylene proton. 3-The prepared compounds were tested as corrosion inhibitors using three techniques. a) Weight loss measurements The data reveals that, the inhibition efficiencies for all prepared cationic surfactants compounds increases with increasing its concentration. The inhibition efficiencies decrease in the temperature rang (30-40ºC) and increase in the temperature rang (40-50ºC). The percentage inhibition efficiency increases by increasing the alkyl chain in the surfactant. The values of inhibition efficiency obtained from the weight loss measurements are in good agreement with those obtained from potentiodynamic polarization method and electrochemical impedance spectroscopy (EIS). The values of activation energy (Ea) were calculated from Arrhenius equation. The data reveals that, the activation energy decrease in the presence of cationic surfactants which indicates that chemical adsorption (strong adsorption of surfactant molecules on the metal surface). The change in enthalpy and entropy of activation values (ΔHo, ΔSo) were calculated from the transition state theory The adsorption of these cationic surfactants on the carbon steel surface obeys the Langmuir adsorption isotherm. Thermodynamic parameters for adsorption process such as free energy (ΔGo ads) enthalpy (ΔHo ads) and entropy (ΔSo ads) for the prepared surfactants were determined. The negative values of ΔGo ads indicating that, the adsorption of surfactants on the metal surface is spontaneous process. All prepared surfactants have positive sign of ΔHo ads indicating that the adsorption of prepared surfactants on the carbon steel surface in 1M HCl solution is endothermic process. The positive sign of ΔSo ads attributed to the increase of disorder due to the adsorption of only one surfactant molecule by desorption of more water molecules. b) Surface tension (γ) The data reveals that the values of surface tension decreases as the activity (concentration) of cationic surfactants increases. The values of effectiveness (ΠCMC), Maximum surface excess (Tmax) and the minimum surface area (Amin) were calculated. The data reveals that the most effective surfactant is one that gives the greater lowering in surface, by increasing the hydrophobic character of the cationic surfactants shifts Γmax to lower concentrations and the minimum area per molecule at the aqueous solution/air interface increases with increasing length of the hydrophobic part. Specific conductivity (K) measurements were performed in order to evaluate the CMC and the degree of counter ion dissociation, β. The data reveals that the degree of dissociation increases by increasing carbon chain length. The values of standard free energy (ΔGo mic) were calculated. The data reveals that the standard free energies of micellization for the synthesized surfactants are always negative, indicating that the micellization is a spontaneous process 3- Antimicrobial Activity Most of the synthesized compounds were evaluated for their antimicrobial activity using the agar diffusion technique (Cooper, 1972). 1 mg/ml solution in dimethyl formamide was used. The tested organisms were Gram-negative bacteria (Escherichia coli, NCTC-10416 & Pseudomonas aerogenasa, NciB9016), Gram-positive bacteria (Bacillus subtilis, NCIB-3610 & Staphylococcus aureus, NCTC-7447) and fungi (Aspergillus niger, ferm-BAM C-21) and unicellular fungi as Candida albicans. The bacteria and fungi were maintained on nutrient agar medium and Czapeks Dox agar medium, respectively. DMF showed no inhibition zones. The agar media were inoculated with different test microorganism. After 24 hrs. of incubation at 30°C for bacteria and 48 hrs. of incubation at 28°C for fungi, the diameter of inhibition zone (mm) was measured. |