4-Aminoantipyrine derived cationic surfactants: Synthesis, characterization, surface activity and screening for potential antimicrobial activities

A series of cationic surfactants were synthesized from chemical modification of 4-aminoantipyrine. The chemical structures were confirmed using infrared (FTIR) and nuclear magnetic resonance (1H NMR) spectroscopy. The surface activities of the surfactants in their solutions were determined by surfac...

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Main Authors: Ismail A. Aiad, Salah M. Tawfik, Mohamed El-Shafie, Abdel Latif A. Rhman
Format: Article
Language:English
Published: Elsevier 2018-09-01
Series:Egyptian Journal of Petroleum
Online Access:http://www.sciencedirect.com/science/article/pii/S1110062117300417
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spelling doaj-257db6c3ebcc4f758da3de584d51dd3f2020-11-24T21:30:05ZengElsevierEgyptian Journal of Petroleum1110-06212018-09-012733273344-Aminoantipyrine derived cationic surfactants: Synthesis, characterization, surface activity and screening for potential antimicrobial activitiesIsmail A. Aiad0Salah M. Tawfik1Mohamed El-Shafie2Abdel Latif A. Rhman3Corresponding author.; Egyptian Petroleum Research Institute, Nasr City, Cairo, EgyptEgyptian Petroleum Research Institute, Nasr City, Cairo, EgyptEgyptian Petroleum Research Institute, Nasr City, Cairo, EgyptEgyptian Petroleum Research Institute, Nasr City, Cairo, EgyptA series of cationic surfactants were synthesized from chemical modification of 4-aminoantipyrine. The chemical structures were confirmed using infrared (FTIR) and nuclear magnetic resonance (1H NMR) spectroscopy. The surface activities of the surfactants in their solutions were determined by surface tension measurements. Increasing the hydrophobic chain length increased the surface activity of the surfactants in solutions. Measurements of interfacial tension between surfactants solutions and light paraffin oil showed that the interfacial tension values were decreased with increasing the alkyl chain length. The emulsion stability measurements showed the applicability of these surfactants as emulsifying agents. The foaming power measurements showed the synthesized surfactants have low ability for foam formation. Thermodynamic properties of adsorption and micellization processes showed their tendency towards adsorption at solution interface and micellization in their solutions. Results showed reasonable surface activities compared to conventional cationic surfactants. The antimicrobial activity of the synthesized surfactants against Gram-positive bacteria (Bacillus subtilis and Staphyl. aureus, Gram-negative bacteria (Pseudomonas aeruginosa and E. coli.) and Fungi (Candida albicans and Aspergillus niger) was evaluated. The efficiency of these compounds as antimicrobial agents) was increased with the hydrophobicity and carbon chain length. Keywords: Antipyrine, Cationic surfactants, Surface, Adsorption, Antimicrobial Activity and CTAB (cetyl trimethyl ammonium bromide)http://www.sciencedirect.com/science/article/pii/S1110062117300417
collection DOAJ
language English
format Article
sources DOAJ
author Ismail A. Aiad
Salah M. Tawfik
Mohamed El-Shafie
Abdel Latif A. Rhman
spellingShingle Ismail A. Aiad
Salah M. Tawfik
Mohamed El-Shafie
Abdel Latif A. Rhman
4-Aminoantipyrine derived cationic surfactants: Synthesis, characterization, surface activity and screening for potential antimicrobial activities
Egyptian Journal of Petroleum
author_facet Ismail A. Aiad
Salah M. Tawfik
Mohamed El-Shafie
Abdel Latif A. Rhman
author_sort Ismail A. Aiad
title 4-Aminoantipyrine derived cationic surfactants: Synthesis, characterization, surface activity and screening for potential antimicrobial activities
title_short 4-Aminoantipyrine derived cationic surfactants: Synthesis, characterization, surface activity and screening for potential antimicrobial activities
title_full 4-Aminoantipyrine derived cationic surfactants: Synthesis, characterization, surface activity and screening for potential antimicrobial activities
title_fullStr 4-Aminoantipyrine derived cationic surfactants: Synthesis, characterization, surface activity and screening for potential antimicrobial activities
title_full_unstemmed 4-Aminoantipyrine derived cationic surfactants: Synthesis, characterization, surface activity and screening for potential antimicrobial activities
title_sort 4-aminoantipyrine derived cationic surfactants: synthesis, characterization, surface activity and screening for potential antimicrobial activities
publisher Elsevier
series Egyptian Journal of Petroleum
issn 1110-0621
publishDate 2018-09-01
description A series of cationic surfactants were synthesized from chemical modification of 4-aminoantipyrine. The chemical structures were confirmed using infrared (FTIR) and nuclear magnetic resonance (1H NMR) spectroscopy. The surface activities of the surfactants in their solutions were determined by surface tension measurements. Increasing the hydrophobic chain length increased the surface activity of the surfactants in solutions. Measurements of interfacial tension between surfactants solutions and light paraffin oil showed that the interfacial tension values were decreased with increasing the alkyl chain length. The emulsion stability measurements showed the applicability of these surfactants as emulsifying agents. The foaming power measurements showed the synthesized surfactants have low ability for foam formation. Thermodynamic properties of adsorption and micellization processes showed their tendency towards adsorption at solution interface and micellization in their solutions. Results showed reasonable surface activities compared to conventional cationic surfactants. The antimicrobial activity of the synthesized surfactants against Gram-positive bacteria (Bacillus subtilis and Staphyl. aureus, Gram-negative bacteria (Pseudomonas aeruginosa and E. coli.) and Fungi (Candida albicans and Aspergillus niger) was evaluated. The efficiency of these compounds as antimicrobial agents) was increased with the hydrophobicity and carbon chain length. Keywords: Antipyrine, Cationic surfactants, Surface, Adsorption, Antimicrobial Activity and CTAB (cetyl trimethyl ammonium bromide)
url http://www.sciencedirect.com/science/article/pii/S1110062117300417
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