Studies on the adsorption and corrosion inhibition of substituted benzylidene schiff bases on mild steel in 1 M HCI / Nor Zakiah Nor Hashim

The objective of this thesis is to investigate the performance of newly synthesized substituted benzylidene Schiff bases as corrosion inhibitors of mild steel in 1 M HC1 at 25°C. To accomplish this intention, a series of (E)-JV’-benzyl idene-A^- phenylbenzene-1,4-diamine Schiff bases that contain d...

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Main Author:	Nor Hashim, Nor Zakiah
Format:	Thesis
Language:	English
Published:	2015
Subjects:	Metals
Online Access:	http://ir.uitm.edu.my/id/eprint/15995/ http://ir.uitm.edu.my/id/eprint/15995/1/TP_NOR%20ZAKIAH%20NIR%20HASHIM%20AS%2015_5.PDF

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recordtype	eprints
spelling	uitm-159952017-01-03T07:54:51Z http://ir.uitm.edu.my/id/eprint/15995/ Studies on the adsorption and corrosion inhibition of substituted benzylidene schiff bases on mild steel in 1 M HCI / Nor Zakiah Nor Hashim Nor Hashim, Nor Zakiah Metals The objective of this thesis is to investigate the performance of newly synthesized substituted benzylidene Schiff bases as corrosion inhibitors of mild steel in 1 M HC1 at 25°C. To accomplish this intention, a series of (E)-JV’-benzyl idene-A^- phenylbenzene-1,4-diamine Schiff bases that contain different substituent groups at para position of benzylidene were synthesized and characterized via physical and spectroscopic analysis. The azomethine double bond (C=N) infrared spectra found for the Schiff bases are at around 1590-1604 cm'1. From *H Nuclear Magnetic Spectroscopy (NMR) spectra, the azomethine proton (singlet) shifted in the range of 8 8.634-8.531 ppm, while the peaks at around 8 157.32-155.82 ppm found in 13C NMR spectra are assigned for azomethine carbon. The corrosion inhibition performance of N-phenyl-1,4-phenylenediamine (NPPD), (£ )- //-benzylidene-V-phenylbenzene-1,4- diamine (Kl), jV-[(£)-4-chlorobenzylidene]-Af-phenylbenzene- 1,4-diamine (K2) and iV-[(£)-4-methoxybenzylidene]-iV-phenylbenzene- 1,4-diamine (K3) was measured in 1 M HC1 using electrochemical methods which are polarization, Linear Polarization (LPR) and Electrochemical Impedance Spectroscopy (EIS). The analysis of substrate’s surface via Scanning Electron Microscopy (SEM), Atomic Force Microscopy (AFM) and X-ray Photoelectron Spectroscopy (XPS) was employed to determine the Schiff base adsorption behaviour on the surface of mild steel in the acidic solution. The electrochemical results revealed that the corrosion inhibition efficiencies of the Schiff bases are higher and achieved up to 96.0% as found for K2,thus more effective than the other Schiff base in the series, and the parent amine of NPPD. The adsorption of inhibitors at the metal-solution interface are well described based on Langmuir adsorption isotherm because R2 and slope values are almost to the value of 1. In further work, the temperature effect of Schiff bases in 1 M HC1 also has been evaluated using polarization method. The inhibition efficiencies found for K2 inhibitor retains its great inhibitive effect and increase slightly until become almost constant at the highest temperature of 55°C. XPS measurements showed that studied Schiff bases mainly adsorbed via chemisorption interaction which involves coordination bond mainly electron donation from n electrons in the benzene ring and azomethine double to the empty orbital of metal. This is supported by AGadS values which suggests the adsorption of Schiff base inhibitors on mild steel surface are due to the both combination of chemisorption and physisorption. The multilayers adsorption of inhibitors is due to subsequent layer physisorbed on the inner most (chemisorbed) layer via weak intermolecular hydrogen bonding of C-H-7T between Schiff base molecules. The relationship between the corrosion inhibition efficiency with physicochemical and electronic properties of TV-phenyl-1,4-phenylenediamine and Schiff bases was examined via density functional theory method. Theoretical results clearly shown that the corrosion inhibition efficiency of inhibitors are essentially depends on the frontier orbitals parameters as example by the increase of inhibition effciency always directly related to the decrease of band gap energy between HOMO and LUMO. It is proven there is an electron transfer interaction among the Schiff base molecules with the active sites at the metal surface 2015 Thesis NonPeerReviewed text en http://ir.uitm.edu.my/id/eprint/15995/1/TP_NOR%20ZAKIAH%20NIR%20HASHIM%20AS%2015_5.PDF Nor Hashim, Nor Zakiah (2015) Studies on the adsorption and corrosion inhibition of substituted benzylidene schiff bases on mild steel in 1 M HCI / Nor Zakiah Nor Hashim. PhD thesis, Universiti Teknologi MARA.
repository_type	Digital Repository
institution_category	Local University
institution	Universiti Teknologi MARA
building	UiTM Institutional Repository
collection	Online Access
language	English
topic	Metals
spellingShingle	Metals Nor Hashim, Nor Zakiah Studies on the adsorption and corrosion inhibition of substituted benzylidene schiff bases on mild steel in 1 M HCI / Nor Zakiah Nor Hashim
description	The objective of this thesis is to investigate the performance of newly synthesized substituted benzylidene Schiff bases as corrosion inhibitors of mild steel in 1 M HC1 at 25°C. To accomplish this intention, a series of (E)-JV’-benzyl idene-A^- phenylbenzene-1,4-diamine Schiff bases that contain different substituent groups at para position of benzylidene were synthesized and characterized via physical and spectroscopic analysis. The azomethine double bond (C=N) infrared spectra found for the Schiff bases are at around 1590-1604 cm'1. From *H Nuclear Magnetic Spectroscopy (NMR) spectra, the azomethine proton (singlet) shifted in the range of 8 8.634-8.531 ppm, while the peaks at around 8 157.32-155.82 ppm found in 13C NMR spectra are assigned for azomethine carbon. The corrosion inhibition performance of N-phenyl-1,4-phenylenediamine (NPPD), (£ )- //-benzylidene-V-phenylbenzene-1,4- diamine (Kl), jV-[(£)-4-chlorobenzylidene]-Af-phenylbenzene- 1,4-diamine (K2) and iV-[(£)-4-methoxybenzylidene]-iV-phenylbenzene- 1,4-diamine (K3) was measured in 1 M HC1 using electrochemical methods which are polarization, Linear Polarization (LPR) and Electrochemical Impedance Spectroscopy (EIS). The analysis of substrate’s surface via Scanning Electron Microscopy (SEM), Atomic Force Microscopy (AFM) and X-ray Photoelectron Spectroscopy (XPS) was employed to determine the Schiff base adsorption behaviour on the surface of mild steel in the acidic solution. The electrochemical results revealed that the corrosion inhibition efficiencies of the Schiff bases are higher and achieved up to 96.0% as found for K2,thus more effective than the other Schiff base in the series, and the parent amine of NPPD. The adsorption of inhibitors at the metal-solution interface are well described based on Langmuir adsorption isotherm because R2 and slope values are almost to the value of 1. In further work, the temperature effect of Schiff bases in 1 M HC1 also has been evaluated using polarization method. The inhibition efficiencies found for K2 inhibitor retains its great inhibitive effect and increase slightly until become almost constant at the highest temperature of 55°C. XPS measurements showed that studied Schiff bases mainly adsorbed via chemisorption interaction which involves coordination bond mainly electron donation from n electrons in the benzene ring and azomethine double to the empty orbital of metal. This is supported by AGadS values which suggests the adsorption of Schiff base inhibitors on mild steel surface are due to the both combination of chemisorption and physisorption. The multilayers adsorption of inhibitors is due to subsequent layer physisorbed on the inner most (chemisorbed) layer via weak intermolecular hydrogen bonding of C-H-7T between Schiff base molecules. The relationship between the corrosion inhibition efficiency with physicochemical and electronic properties of TV-phenyl-1,4-phenylenediamine and Schiff bases was examined via density functional theory method. Theoretical results clearly shown that the corrosion inhibition efficiency of inhibitors are essentially depends on the frontier orbitals parameters as example by the increase of inhibition effciency always directly related to the decrease of band gap energy between HOMO and LUMO. It is proven there is an electron transfer interaction among the Schiff base molecules with the active sites at the metal surface
format	Thesis
author	Nor Hashim, Nor Zakiah
author_facet	Nor Hashim, Nor Zakiah
author_sort	Nor Hashim, Nor Zakiah
title	Studies on the adsorption and corrosion inhibition of substituted benzylidene schiff bases on mild steel in 1 M HCI / Nor Zakiah Nor Hashim
title_short	Studies on the adsorption and corrosion inhibition of substituted benzylidene schiff bases on mild steel in 1 M HCI / Nor Zakiah Nor Hashim
title_full	Studies on the adsorption and corrosion inhibition of substituted benzylidene schiff bases on mild steel in 1 M HCI / Nor Zakiah Nor Hashim
title_fullStr	Studies on the adsorption and corrosion inhibition of substituted benzylidene schiff bases on mild steel in 1 M HCI / Nor Zakiah Nor Hashim
title_full_unstemmed	Studies on the adsorption and corrosion inhibition of substituted benzylidene schiff bases on mild steel in 1 M HCI / Nor Zakiah Nor Hashim
title_sort	studies on the adsorption and corrosion inhibition of substituted benzylidene schiff bases on mild steel in 1 m hci / nor zakiah nor hashim
publishDate	2015
url	http://ir.uitm.edu.my/id/eprint/15995/ http://ir.uitm.edu.my/id/eprint/15995/1/TP_NOR%20ZAKIAH%20NIR%20HASHIM%20AS%2015_5.PDF
first_indexed	2023-09-18T22:55:07Z
last_indexed	2023-09-18T22:55:07Z
_version_	1777417802357932032

Studies on the adsorption and corrosion inhibition of substituted benzylidene schiff bases on mild steel in 1 M HCI / Nor Zakiah Nor Hashim

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