Nuclear chemistry

Catalysis

Adsorption

Carbon steel

Composite number

Antimicrobial

Electrochemistry

Materials science

Biochemistry

Carbon fibers

Inorganic chemistry

Physical chemistry

Polymer

Combinatorial chemistry

Cationic polymerization

Tafel equation

Organic chemistry

Composite material

Pulmonary surfactant

Mannich base

Mannich reaction

Corrosion

Chemistry

Electrode

Monomer

Journal of Molecular Liquids

Morpholinomethylnaphthalene-1-ol (MMN-OH) and 2, 6-Bismorpholinomethyl naphthalene-1, 5-diol (BMND-OH) were synthesized via Mannich reaction. The novel monomeric cationic surfactant (DHNMMB) and gemini cationic surfactant (DHNBMBDMB) were obtained based on the previous Mannich compounds through quaternization reaction. The resulting structures confirmed by IR, 1HNMR, and mass spectroscopies. Gravimetric and electrochemical techniques were utilized to assess the inhibitory activity of the synthesized surfactants on CS deterioration in 5% HCl. We note that DHNBMBDMB is better than DHNMMB. This is due to the chemical structure and surface properties. The maximum inhibition performance of DHNBMBDMB and DHNMMB at 2.5 × 10−3 M is 96.14 and 94.65%, respectively. Tafel curves indicated that the DHNMMB and DHNBMBDMB were hybrid-type inhibitors. Adsorption of DHNMMB and DHNBMBDMB onto CS surface obey Langmuir model. Both DFT and MC simulation studies of DHNMMB and DHNBMBDMB compounds are discussed thoroughly and agree with the laboratory experimental corrosion tests. SEM & AFM photos show a good CS surface in the presence of DHNMMB and DHNBMBDMB versus the absence of them. The antimicrobial activities of all the synthesized Mannich bases and their surfactants were tested. The surfactants had a talented effect against Candida albicans.

Novel macrocyclic cationic surfactants: Synthesis, experimental and theoretical studies of their corrosion inhibition activity for carbon steel and their antimicrobial activities