Investigation of substituent position effects of Schiff base compounds on mild steel corrosion

In this study, three new Schiff base ligands namely 1-((1E)-((8-((2-hydroxybenzylidene)amino)naphthalen-1-yl)imino)methyl)naphthalen-2-ol (L1-2HB), 1-((1E)-((8-((3-hydroxybenzylidene)amino)naphthalen-1-yl)imino)methyl)naphthalen-2-ol (L2-3HB) and 1-((1E)-((8-((4-hydroxybenzylidene)amino)naphthalen-1...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Rashid, Shadatul Hanom, Ishak, Siti Khadijah
Format: Tagungsbericht
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 1
container_start_page
container_title
container_volume 2614
creator Rashid, Shadatul Hanom
Ishak, Siti Khadijah
description In this study, three new Schiff base ligands namely 1-((1E)-((8-((2-hydroxybenzylidene)amino)naphthalen-1-yl)imino)methyl)naphthalen-2-ol (L1-2HB), 1-((1E)-((8-((3-hydroxybenzylidene)amino)naphthalen-1-yl)imino)methyl)naphthalen-2-ol (L2-3HB) and 1-((1E)-((8-((4-hydroxybenzylidene)amino)naphthalen-1-yl)imino)methyl)naphthalen-2-ol (L3-4HB) were synthesized through two-steps process via reflux-reaction. 1H Nuclear Magnetic Resonance (1H NMR) and Fourier Transform Infrared (FTIR) Spectroscopies were used to characterize the synthesized Schiff base ligands and the inhibitory effect of mild steel in 1.0 M hydrochloric acid (HCl) and 1.0 M sodium chloride (NaCl) solutions in the presence of varying concentrations of Schiff bases as corrosion inhibitor was investigated at room temperature using weight loss method. The existence of imine group in the range of 1620 – 1625 cm−1 on IR spectrum revealed the formation of the azomethine linkage indicating the desired compound was successfully achieved. These Schiff base compounds significantly inhibited mild steel corrosion in both solutions. The efficiency of inhibition was observed to improve as the inhibitor concentration was increased. Weight loss analysis confirmed that the Schiff base compounds have effective inhibitory abilities for mild steel in HCl and NaCl medium, with a maximum inhibition efficiency of 99 and 96 % at 0.1 M of additive concentration. The pattern of maximum inhibition efficiency for both solutions increase in the order of ortho>para>meta substituted. According to the experimental findings, it can be proposed that the Schiff base ligand (L1-2HB) containing electron donating substituent at appropriate position exhibited excellent inhibitory action on mild steel surface in the medium investigated.
doi_str_mv 10.1063/5.0127507
format Conference Proceeding
fullrecord <record><control><sourceid>proquest_scita</sourceid><recordid>TN_cdi_scitation_primary_10_1063_5_0127507</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2826494468</sourcerecordid><originalsourceid>FETCH-LOGICAL-p168t-6936f03687e78b563028a43e3a6abab92b91633b29a5fa1fb1875fddcb7b72973</originalsourceid><addsrcrecordid>eNp9kElLBDEQhYMoOI4e_AcBb0KPWTrbUQaXgQEPKngyJN2J9jDTaZO04L83s4A3T0XV-6qK9wC4xGiGEac3bIYwEQyJIzDBjOFKcMyPwQQhVVekpm-n4CylFUJECSEn4H3Rf7uUuw-Tu9DD4GEabenz6PoMh5C63dx575qctvpz89l5D61JDjZhM4Sxb4vQw023bmHKzq3LPMayGvpzcOLNOrmLQ52C1_u7l_ljtXx6WMxvl9WAucwVV5R7RLkUTkjLOEVEmpo6arixxipiFeaUWqIM8wZ7i6Vgvm0bK6woTugUXO3vDjF8jcWQXoUx9uWlJpLwWtU1l4W63lOp6fLOsB5itzHxR2Okt_lppg_5_Qd_h_gH6qH19Bf6ZXIA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>conference_proceeding</recordtype><pqid>2826494468</pqid></control><display><type>conference_proceeding</type><title>Investigation of substituent position effects of Schiff base compounds on mild steel corrosion</title><source>AIP Journals Complete</source><creator>Rashid, Shadatul Hanom ; Ishak, Siti Khadijah</creator><contributor>Shimizu, Kinya ; Sugianto ; Cahyono, Edy ; Masturi ; Lam, Cher Ping ; Aazmi, Shafiq</contributor><creatorcontrib>Rashid, Shadatul Hanom ; Ishak, Siti Khadijah ; Shimizu, Kinya ; Sugianto ; Cahyono, Edy ; Masturi ; Lam, Cher Ping ; Aazmi, Shafiq</creatorcontrib><description>In this study, three new Schiff base ligands namely 1-((1E)-((8-((2-hydroxybenzylidene)amino)naphthalen-1-yl)imino)methyl)naphthalen-2-ol (L1-2HB), 1-((1E)-((8-((3-hydroxybenzylidene)amino)naphthalen-1-yl)imino)methyl)naphthalen-2-ol (L2-3HB) and 1-((1E)-((8-((4-hydroxybenzylidene)amino)naphthalen-1-yl)imino)methyl)naphthalen-2-ol (L3-4HB) were synthesized through two-steps process via reflux-reaction. 1H Nuclear Magnetic Resonance (1H NMR) and Fourier Transform Infrared (FTIR) Spectroscopies were used to characterize the synthesized Schiff base ligands and the inhibitory effect of mild steel in 1.0 M hydrochloric acid (HCl) and 1.0 M sodium chloride (NaCl) solutions in the presence of varying concentrations of Schiff bases as corrosion inhibitor was investigated at room temperature using weight loss method. The existence of imine group in the range of 1620 – 1625 cm−1 on IR spectrum revealed the formation of the azomethine linkage indicating the desired compound was successfully achieved. These Schiff base compounds significantly inhibited mild steel corrosion in both solutions. The efficiency of inhibition was observed to improve as the inhibitor concentration was increased. Weight loss analysis confirmed that the Schiff base compounds have effective inhibitory abilities for mild steel in HCl and NaCl medium, with a maximum inhibition efficiency of 99 and 96 % at 0.1 M of additive concentration. The pattern of maximum inhibition efficiency for both solutions increase in the order of ortho&gt;para&gt;meta substituted. According to the experimental findings, it can be proposed that the Schiff base ligand (L1-2HB) containing electron donating substituent at appropriate position exhibited excellent inhibitory action on mild steel surface in the medium investigated.</description><identifier>ISSN: 0094-243X</identifier><identifier>EISSN: 1551-7616</identifier><identifier>DOI: 10.1063/5.0127507</identifier><identifier>CODEN: APCPCS</identifier><language>eng</language><publisher>Melville: American Institute of Physics</publisher><subject>Corrosion ; Corrosion effects ; Corrosion inhibitors ; Corrosion tests ; Efficiency ; Fourier transforms ; Hydrochloric acid ; Hydrogen chloride ; Imines ; Investigations ; Ligands ; Low carbon steels ; NMR ; Nuclear magnetic resonance ; Protons ; Room temperature ; Sodium chloride ; Weight loss</subject><ispartof>AIP conference proceedings, 2023, Vol.2614 (1)</ispartof><rights>Author(s)</rights><rights>2023 Author(s). Published by AIP Publishing.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://pubs.aip.org/acp/article-lookup/doi/10.1063/5.0127507$$EHTML$$P50$$Gscitation$$H</linktohtml><link.rule.ids>309,310,314,780,784,789,790,794,4510,23929,23930,25139,27923,27924,76155</link.rule.ids></links><search><contributor>Shimizu, Kinya</contributor><contributor>Sugianto</contributor><contributor>Cahyono, Edy</contributor><contributor>Masturi</contributor><contributor>Lam, Cher Ping</contributor><contributor>Aazmi, Shafiq</contributor><creatorcontrib>Rashid, Shadatul Hanom</creatorcontrib><creatorcontrib>Ishak, Siti Khadijah</creatorcontrib><title>Investigation of substituent position effects of Schiff base compounds on mild steel corrosion</title><title>AIP conference proceedings</title><description>In this study, three new Schiff base ligands namely 1-((1E)-((8-((2-hydroxybenzylidene)amino)naphthalen-1-yl)imino)methyl)naphthalen-2-ol (L1-2HB), 1-((1E)-((8-((3-hydroxybenzylidene)amino)naphthalen-1-yl)imino)methyl)naphthalen-2-ol (L2-3HB) and 1-((1E)-((8-((4-hydroxybenzylidene)amino)naphthalen-1-yl)imino)methyl)naphthalen-2-ol (L3-4HB) were synthesized through two-steps process via reflux-reaction. 1H Nuclear Magnetic Resonance (1H NMR) and Fourier Transform Infrared (FTIR) Spectroscopies were used to characterize the synthesized Schiff base ligands and the inhibitory effect of mild steel in 1.0 M hydrochloric acid (HCl) and 1.0 M sodium chloride (NaCl) solutions in the presence of varying concentrations of Schiff bases as corrosion inhibitor was investigated at room temperature using weight loss method. The existence of imine group in the range of 1620 – 1625 cm−1 on IR spectrum revealed the formation of the azomethine linkage indicating the desired compound was successfully achieved. These Schiff base compounds significantly inhibited mild steel corrosion in both solutions. The efficiency of inhibition was observed to improve as the inhibitor concentration was increased. Weight loss analysis confirmed that the Schiff base compounds have effective inhibitory abilities for mild steel in HCl and NaCl medium, with a maximum inhibition efficiency of 99 and 96 % at 0.1 M of additive concentration. The pattern of maximum inhibition efficiency for both solutions increase in the order of ortho&gt;para&gt;meta substituted. According to the experimental findings, it can be proposed that the Schiff base ligand (L1-2HB) containing electron donating substituent at appropriate position exhibited excellent inhibitory action on mild steel surface in the medium investigated.</description><subject>Corrosion</subject><subject>Corrosion effects</subject><subject>Corrosion inhibitors</subject><subject>Corrosion tests</subject><subject>Efficiency</subject><subject>Fourier transforms</subject><subject>Hydrochloric acid</subject><subject>Hydrogen chloride</subject><subject>Imines</subject><subject>Investigations</subject><subject>Ligands</subject><subject>Low carbon steels</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Protons</subject><subject>Room temperature</subject><subject>Sodium chloride</subject><subject>Weight loss</subject><issn>0094-243X</issn><issn>1551-7616</issn><fulltext>true</fulltext><rsrctype>conference_proceeding</rsrctype><creationdate>2023</creationdate><recordtype>conference_proceeding</recordtype><recordid>eNp9kElLBDEQhYMoOI4e_AcBb0KPWTrbUQaXgQEPKngyJN2J9jDTaZO04L83s4A3T0XV-6qK9wC4xGiGEac3bIYwEQyJIzDBjOFKcMyPwQQhVVekpm-n4CylFUJECSEn4H3Rf7uUuw-Tu9DD4GEabenz6PoMh5C63dx575qctvpz89l5D61JDjZhM4Sxb4vQw023bmHKzq3LPMayGvpzcOLNOrmLQ52C1_u7l_ljtXx6WMxvl9WAucwVV5R7RLkUTkjLOEVEmpo6arixxipiFeaUWqIM8wZ7i6Vgvm0bK6woTugUXO3vDjF8jcWQXoUx9uWlJpLwWtU1l4W63lOp6fLOsB5itzHxR2Okt_lppg_5_Qd_h_gH6qH19Bf6ZXIA</recordid><startdate>20230616</startdate><enddate>20230616</enddate><creator>Rashid, Shadatul Hanom</creator><creator>Ishak, Siti Khadijah</creator><general>American Institute of Physics</general><scope>8FD</scope><scope>H8D</scope><scope>L7M</scope></search><sort><creationdate>20230616</creationdate><title>Investigation of substituent position effects of Schiff base compounds on mild steel corrosion</title><author>Rashid, Shadatul Hanom ; Ishak, Siti Khadijah</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p168t-6936f03687e78b563028a43e3a6abab92b91633b29a5fa1fb1875fddcb7b72973</frbrgroupid><rsrctype>conference_proceedings</rsrctype><prefilter>conference_proceedings</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Corrosion</topic><topic>Corrosion effects</topic><topic>Corrosion inhibitors</topic><topic>Corrosion tests</topic><topic>Efficiency</topic><topic>Fourier transforms</topic><topic>Hydrochloric acid</topic><topic>Hydrogen chloride</topic><topic>Imines</topic><topic>Investigations</topic><topic>Ligands</topic><topic>Low carbon steels</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Protons</topic><topic>Room temperature</topic><topic>Sodium chloride</topic><topic>Weight loss</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rashid, Shadatul Hanom</creatorcontrib><creatorcontrib>Ishak, Siti Khadijah</creatorcontrib><collection>Technology Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rashid, Shadatul Hanom</au><au>Ishak, Siti Khadijah</au><au>Shimizu, Kinya</au><au>Sugianto</au><au>Cahyono, Edy</au><au>Masturi</au><au>Lam, Cher Ping</au><au>Aazmi, Shafiq</au><format>book</format><genre>proceeding</genre><ristype>CONF</ristype><atitle>Investigation of substituent position effects of Schiff base compounds on mild steel corrosion</atitle><btitle>AIP conference proceedings</btitle><date>2023-06-16</date><risdate>2023</risdate><volume>2614</volume><issue>1</issue><issn>0094-243X</issn><eissn>1551-7616</eissn><coden>APCPCS</coden><abstract>In this study, three new Schiff base ligands namely 1-((1E)-((8-((2-hydroxybenzylidene)amino)naphthalen-1-yl)imino)methyl)naphthalen-2-ol (L1-2HB), 1-((1E)-((8-((3-hydroxybenzylidene)amino)naphthalen-1-yl)imino)methyl)naphthalen-2-ol (L2-3HB) and 1-((1E)-((8-((4-hydroxybenzylidene)amino)naphthalen-1-yl)imino)methyl)naphthalen-2-ol (L3-4HB) were synthesized through two-steps process via reflux-reaction. 1H Nuclear Magnetic Resonance (1H NMR) and Fourier Transform Infrared (FTIR) Spectroscopies were used to characterize the synthesized Schiff base ligands and the inhibitory effect of mild steel in 1.0 M hydrochloric acid (HCl) and 1.0 M sodium chloride (NaCl) solutions in the presence of varying concentrations of Schiff bases as corrosion inhibitor was investigated at room temperature using weight loss method. The existence of imine group in the range of 1620 – 1625 cm−1 on IR spectrum revealed the formation of the azomethine linkage indicating the desired compound was successfully achieved. These Schiff base compounds significantly inhibited mild steel corrosion in both solutions. The efficiency of inhibition was observed to improve as the inhibitor concentration was increased. Weight loss analysis confirmed that the Schiff base compounds have effective inhibitory abilities for mild steel in HCl and NaCl medium, with a maximum inhibition efficiency of 99 and 96 % at 0.1 M of additive concentration. The pattern of maximum inhibition efficiency for both solutions increase in the order of ortho&gt;para&gt;meta substituted. According to the experimental findings, it can be proposed that the Schiff base ligand (L1-2HB) containing electron donating substituent at appropriate position exhibited excellent inhibitory action on mild steel surface in the medium investigated.</abstract><cop>Melville</cop><pub>American Institute of Physics</pub><doi>10.1063/5.0127507</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0094-243X
ispartof AIP conference proceedings, 2023, Vol.2614 (1)
issn 0094-243X
1551-7616
language eng
recordid cdi_scitation_primary_10_1063_5_0127507
source AIP Journals Complete
subjects Corrosion
Corrosion effects
Corrosion inhibitors
Corrosion tests
Efficiency
Fourier transforms
Hydrochloric acid
Hydrogen chloride
Imines
Investigations
Ligands
Low carbon steels
NMR
Nuclear magnetic resonance
Protons
Room temperature
Sodium chloride
Weight loss
title Investigation of substituent position effects of Schiff base compounds on mild steel corrosion
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T02%3A35%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_scita&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=proceeding&rft.atitle=Investigation%20of%20substituent%20position%20effects%20of%20Schiff%20base%20compounds%20on%20mild%20steel%20corrosion&rft.btitle=AIP%20conference%20proceedings&rft.au=Rashid,%20Shadatul%20Hanom&rft.date=2023-06-16&rft.volume=2614&rft.issue=1&rft.issn=0094-243X&rft.eissn=1551-7616&rft.coden=APCPCS&rft_id=info:doi/10.1063/5.0127507&rft_dat=%3Cproquest_scita%3E2826494468%3C/proquest_scita%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2826494468&rft_id=info:pmid/&rfr_iscdi=true