Synthesis, Characterisation and Corrosion Inhibition of Mild Steel by Butyltin(IV) 2-Acetylpyridine 4-Methyl-3-Thiosemicarbazone in HCl

Authors

  • Nur Nadira Hazani Faculty of Applied Sciences, Universiti Teknologi MARA, Shah Alam, Selangor 40450, Malaysia
  • Nur Nadia Dzulkifli School of Chemistry and Environment, Faculty of Applied Sciences, Universiti Teknologi MARA Cawangan Negeri Sembilan, Kampus Kuala Pilah, Pekan Parit Tinggi, Kuala Pilah, Negeri Sembilan 72000, Malaysia
  • Sheikh Ahmad Izaddin Sheikh Mohd Ghazali School of Chemistry and Environment, Faculty of Applied Sciences, Universiti Teknologi MARA Cawangan Negeri Sembilan, Kampus Kuala Pilah, Pekan Parit Tinggi, Kuala Pilah, Negeri Sembilan 72000, Malaysia
  • Yusairie Mohd Faculty of Applied Sciences, Universiti Teknologi MARA, Shah Alam, Selangor 40450, Malaysia

DOI:

https://doi.org/10.48048/tis.2022.4615

Keywords:

Organotin (IV), Thiosemicarbazone, Corrosion, EIS, Langmuir isotherm

Abstract

Schiff base ligand, 2-acetylpyridine 4-methyl-3-thiosemicarbazone (Me-LH), and its organotin complex (BuSn(Me-LH)Cl2) were synthesized, characterized, and subjected to corrosion inhibition study. The spectra and crystal structure obtained revealed that the ligand is coordinated by pyridyl nitrogen, azomethine nitrogen, and thiolate sulfur to organotin (IV) ion. Corrosion inhibition of the synthesized compounds on mild steels in 1 M HCl solution at different concentrations were tested using weight loss, Electrochemical Impedance Spectroscopy (EIS), potentiodynamic polarization, Scanning Electron Microscopy (SEM) and adsorption analyses. Corrosion inhibition results showed that the complex had a strong corrosion inhibitory effect in comparison to the ligand. The inhibition efficiency of all the techniques improved with an increase in the concentration of corrosion inhibitor. Polarization analysis results showed that the compounds can be categorized as mixed-type inhibitors. Meanwhile, the EIS study indicates that with an increase in the concentration of corrosion inhibitor, the resistance to charge transfer increased. This resulted in the adsorption of inhibitors and the development of a protective layer on the mild steel surface which was further confirmed by SEM analysis. The adsorption isotherm of compounds on a mild steel surface followed the Langmuir isotherm model.

HIGHLIGHTS

  • The efficient method to inhibit the corrosion rate of mild steel in an acidic medium is a corrosion inhibitor
  • The electrochemical and weight loss analysis proved that the corrosion inhibition efficiency increases when the concentration of inhibitor is increased
  • The study proved that the thiosemicarbazone complex showed the potential as corrosion inhibitors at low concentrations


GRAPHICAL ABSTRACT

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

References

MP Binsi, TK Joby, K Ragi, VC Sini and J Reeja. Interaction of two heterocyclic Schiff bases derived from 2-acetyl pyridine on mild steel in hydrochloric acid: Physicochemical and corrosion inhibition investigations. Curr. Chem. Lett. 2020; 9, 19-30.

NN Hazani, Y Mohd, SAIS Ghazali. Electrochemical studies of thiosemicarbazone derivative and its tin(IV) complex as corrosion inhibitor for mild steel in 1 M hydrochloric acid. Chem. J. Mold. 2019; 14, 98-106.

KF Khaled, OA Elhabib, A El-mghraby, OB Ibrahim and MAM Ibrahim. Inhibitive effect of thiosemicarbazone derivative on corrosion of mild steel in hydrochloric acid solution. J. Mater. Environ. Sci. 2010; 1, 139-50.

Y Meng, W Ning, B Xu, W Yang, K Zhang, Y Chen, L Li, X Liu, J Zheng and Y Zhang. Inhibition of mild steel corrosion in hydrochloric acid using two novel pyridine Schiff base derivatives: A comparative study of experimental and theoretical results. RSC Adv. 2017; 7, 43014-29.

AEAS Fouda, AAE Samir, HE Elsherbiny, AE Hazem and SA Ashraf. Experimental and surface morphological studies of corrosion inhibition on carbon steel in HCl solution using some new hydrazide derivatives. RSC Adv. 2021; 11, 13497-512.

A Dadgarinezhad and F Baghaei. A new synthesized corrosion inhibitor for mild steel in 0.5 M H2SO4. Gazi Univ. J. Sci. 2011; 24, 219-26.

S Kumar, H Vashisht, LO Olasunkanmi, I Bahadur, H Verma, G Singh, IB Obot and EE Ebenso. Experimental and theoretical studies on inhibition of mild steel corrosion by some synthesized polyurethane tri-block co-polymers. Sci. Rep. 2016; 6, 1-18.

P Mourya, S Banerjee, RB Rastogi and MM Singh. Inhibition of mild steel corrosion in hydrochloric and sulfuric acid media using a thiosemicarbazone derivative. Ind. Eng. Chem. Res. 2013; 52, 12733-47.

SV Sanap, RM Patil and RAMS Dubey. Corrosion inhibition of mild steel by using mixed ligand metal complexes. Int. J. Chem. Sci. 2013; 1, 503-17.

EA Florez-Frias, V Barba, R Lopez-Sesenes, LL Landeros-Martínez, JP Flores-De los Ríos, M Casales and JG Gonzalez-Rodriguez. Use of a metallic complex derived from curcuma longa as green corrosion inhibitor for carbon steel in sulfuric acid. Int. J. Corros. 2021; 2021, 1-13.

MH Mahross, K Efil, TAS El-nasr and OA Abbas. Experimental and theoretical study on corrosion inhibition of mild steel in oilfield formation water using some Schiff base metal complexes. J. Electrochem. Sci. Technol. 2017; 8, 222-35.

RB Rastogi, K Singh and JL Maurya. Synthesis and characterization of organotin(IV) thiobiurets. Synth. React. Inorg. M. 2012; 42, 616-20.

KL Rajesh and KS Amirthagadeswaran. Corrosion and wear behaviour of nano Al2O3 reinforced copper metal matrix composites synthesized by high energy ball milling. Part. Sci. Technol. 2019; 1-8.

M Benabdellah, A Yahyi, A Dafali, A Aouniti, B Hammouti and A Ettouhami. Corrosion inhibition of steel in molar HCl by triphenyltin2-thiophene carboxylate. Arab. J. Chem. 2011; 4, 243-47.

H Kurniasih, M Nurissalam, B Iswantoro, H Afriyani, HI Qudus and S Hadi. The synthesis, characterization and comparative anticorrosion study of some organotin(IV) 4-chlorobenzoates. Orient. J. Chem. 2015; 31, 2377-83.

RB Rastogi, MM Singh, K Singh and M Yadav. Organotin dithiobiurets as corrosion inhibitors for mild steel-dimethyl sulfoxide containing HCl. Afr. J. Pure Appl. Chem. 2011; 5, 19-33.

S Hadi, H Afriyani, HI Qudus and Noviany. The anticorrosion activity of dibutyltin(IV) and diphenyltin(IV) dihydroxybenzoate compounds towards HRP mild steel in NaCl. J. Chem. Pharm. Res. 2016; 8, 975-80.

S Hadi, H Afriyani, DW Anggraini, IH Qudus and T Suhartati. Synthesis and potency study of some dibutyltin(IV) dinitrobenzoate compounds as corrosion inhibitor for mild steel HRP in DMSO-HCl solution. Asian J. Chem. 2015; 27, 1509-12.

Bruker. 2009. SMART, SAINT and SADABS. Bruker AXS, Madison, Wisconsin, USA.

AL Spek. Structure validation in chemical crystallography. Acta Cryst. D: Biol. Cryst. 2009; 65, 148-55.

NN Hazani, NN Dzulkifli, SAISM Ghazali, Y Mohd, Y Farina and F Ngatiman. Synthesis, characterisation, crystal structure and anti-corrosion studies of an organotin (IV) complex of 2-acetylpyridine 4-ethyl-3- thiosemicarbazone (LH): N-BuSn (L)Cl2. ASM Sci. J. 2019; 12, 1-15.

D Daoud, T Douadi, H Hamani, S Chafaa and M Al-noaimi. Corrosion inhibition of mild steel by two new S-heterocyclic compounds in 1 M HCl: Experimental and computational study. Corros. Sci. 2015; 94, 21-37.

M Muralisankar, R Sreedharan and S Sujith. N(1)-pentyl isatin-N(4)-methyl-N(4)-phenyl thiosemicarbazone (PITSc) as a corrosion inhibitor on mild steel in HCl. J. Alloys Compd. 2017; 695, 171-82.

NZN Hashim, K Kassim and Y Mohd. Corrosion inhibition of mild steel by N-phenyl-1,4-phenylenediamine and its Schiff base derivatives in 1 M HCl. Adv. Mat. Res. 2012; 554-556, 408-13.

A Paul, TK Joby, VP Raphael and KS Shaju. Electrochemical and gravimetric corrosion inhibition investigations of a heterocyclic Schiff base derived from 3-formylindole. IOSR J. Appl. Chem. 2012; 1, 17-23.

EE Ebenso, DA Isabirye and NO Eddy. Adsorption and quantum chemical studies on the inhibition potentials of some thiosemicarbazides for the corrosion of mild steel in acidic medium. Int. J. Mol. Sci. 2010; 11, 2473-98.

A Manivel, S Ramkumar, JJ Wu, AM Asiri and S Anandan. Exploration of (S)-4,5,6,7-tetrahydrobenzo[d]thiazole-2,6-diamine as feasible corrosion inhibitor for mild steel in acidic media. J. Environ. Chem. Eng. 2014; 2, 463-70.

SA Aly and SK Fathalla. Preparation, characterization of some transition metal complexes of hydrazone derivatives and their antibacterial and antioxidant activities. Arab. J. Chem. 2020; 13, 3735-50.

LNDA Neto, MDCAD Lima, JFD Oliveira, ERD Souza, MDS Buonafina, MNV Anjos, FA Brayner, LC Alves, RP Neves and FJB Mendonca-Junior. Synthesis, cytotoxicity and antifungal activity of 5-nitro-thiophene-thiosemicarbazones derivatives. Chem. Biol. Interact. 2017; 272, 172-81.

AQ Ali, SG Teoh, A Salhin and N Eltayeb. Synthesis of platinum(II) complexes of isatin thiosemicarbazones derivatives: In vitro anti-cancer and deoxyribosenucleic acid binding activities. Inorganica Chim. Acta 2014; 146, 235-44.

HP Ebrahimi, JS Hadi, TA Alsalim, TS Ghali and Z Bolandnazar. A novel series of thiosemicarbazone drugs: From synthesis to structure. Spectrochim. Acta A Mol. Biomol. Spectrosc. 2015; 137, 1067-77.

PP Netalkar, SP Netalkar and VK Revankar. Transition metal complexes of thiosemicarbazone: Synthesis, structures and invitro antimicrobial studies. Polyhedron 2015; 100, 215-22.

K Sampath, S Sathiyaraj, G Raja and C Jayabalakrishnan. Mixed ligand ruthenium(III) complexes of benzaldehyde 4-methyl-3-thiosemicarbazones with triphenylphosphine/triphenylarsine co-ligands: Synthesis, DNA binding, DNA cleavage, antioxidative and cytotoxic activity. J. Mol. Struct. 2013; 1046, 82-91.

YY Wu, YT Wang, YY Wang, MX Li, YL Lu and YH Zhang. Dimethyltin(IV) and palladium(II) complexes derived from 2-benzoylpyridine N(4)-cyclohexylthiosemicarbazone: Synthesis, crystal structures and biological evaluation. Inorg. Chem. Commun. 2017; 78, 65-9.

GL Parrilha, JG Da Silva, LF Gouveia, AK Gasparoto, RP Dias, WR Rocha, DA Santos, NL Speziali and H Beraldo. Pyridine-derived thiosemicarbazones and their tin(IV) complexes with antifungal activity against Candida spp. Eur. J. Med. Chem. 2011; 46, 1473-82.

MA Affan, FS Wan, Z Ngaini and M Shamsuddin. Synthesis, characterization and biological studies of organotin(IV) complexes of thiosemicarbazone ligand derived from pyruvic acid: X-ray crystal structure of [Me2Sn(PAT)]. Malaysian J. Anal. Sci. 2009; 13, 63-72.

K Venkatesh, P Rayam, KBC Sekhar and K Mukkanti. Synthesis, characterization and biological activity of some new thiosemicarbazide derivatives and their transition metal complexes. Int. J. Appl. Biol. Pharm. Tech. 2016; 7, 258-67.

MA Salam, MA Affan, R Saha, FB Ahmad and N Sam. Synthesis, characterization and in vitro antibacterial studies of organotin(IV) complexes with 2-hydroxyacetophenone-2-methylphenylthiosemicarbazone (H2dampt). Bioinorg. Chem. Appl. 2012; 2012, 1-9.

SA Hosseini-Yazdi, S Hosseinpour, AA Khandar and J White. Synthesis, characterization, and X-ray crystal structures of copper(II) and nickel(II) complexes with two bis(thiosemicarbazone) ligands and investigation of their electrochemical behavior. Transit. Met. Chem. 2016; 41, 65-75.

SA Hosseini-Yazdi, S Hosseinpour, AA Khandar, WS Kassel and NA Piro. Copper(II) and nickel(II) complexes with two new bis(thiosemicarbazone) ligands: Synthesis, characterization, X-ray crystal structures and their electrochemistry behavior. Inorganica Chim. Acta. 2015; 427, 124-30.

O Abdalla, Y Farina and N Ibrahim. Synthesis, characterization and antibacterial study of copper(II) complexes of thiosemicarbazones. Malaysian J. Anal. Sci. 2015; 19, 1171-8.

HL Singh, JB Singh and KP Sharma. Synthetic, structural, and antimicrobial studies of organotin(IV) complexes of semicarbazone, thiosemicarbazone derived from 4-hydroxy-3- methoxybenzaldehyde. Res. Chem. Intermed. 2012; 38, 53-65.

S Wang, QL Li, RF Zhang, JY Du, YX Li and CL Ma. Novel organotin(IV) complexes derived from 4-carboxybenzenesulfonamide: Synthesis, structure and in vitro cytostatic activity evaluation. Polyhedron 2019; 158, 15-24.

DG Calatayud, E López-Torres, MA Mendiola and JR Procopio. Tin(IV) complexes with thiosemicarbazide and 4-methyl-3-thiosemicarbazide derivatives. Z. Anorg. Allg. Chem. 2007; 633, 1925-31.

N Khan, Y Farina, LK Mun, NF Rajab and N Awang. Syntheses, characterization, X-ray diffraction studies and in vitro antitumor activities of diorganotin(IV) derivatives of bis(p-substituted-N-methylbenzylaminedithiocarbamates). Polyhedron 2015; 85, 754-760.

W Rehman, MK Baloch and A Badshah. Synthesis, spectral characterization and bio-analysis of some organotin(IV) complexes. Eur. J. Med. Chem. 2008; 43, 2380-85.

AD Khalaji, G Grivani, SJ Akerdi, K Gotoh, H Ishida and H Mighani. Synthesis, spectroscopic characterization, crystal structures, and theoretical studies of (E)-2-(2,4-dimethoxybenzylidene) thiosemicarbazone and (E)-2-(2,5-dimethoxybenzylidene)thiosemicarbazone. Struct. Chem. 2010; 21, 995-1003.

MA Affan, MA Salam, FB Ahmad, F White and HM Ali. Organotin(IV) complexes of 2-hydroxyacetophenone-N(4)-cyclohexylthiosemicarbazone (H2dact): Synthesis, spectral characterization, crystal structure and biological studies. Inorganica Chim. Acta. 2012; 387, 219-25.

MHSA Hamid, ANAH Said, AH Mirza, MR Karim, M Arifuzzaman, MA Ali and PV Bernhardt. Synthesis, structures and spectroscopic properties of some tin(IV) complexes of the 2-acetylpyrazine Schiff bases of S-methyl- and S-benzyldithiocarbazates. Inorganica Chim. Acta. 2016; 453, 742-50.

MX Li, D Zhang, LZ Zhang, JY Niu and BS Ji. Diorganotin(IV) complexes with 2-benzoylpyridine and 2-acetylpyrazine N(4)-phenylthiosemicarbazones: Synthesis, crystal structures and biological activities. J. Organomet. Chem. 2011; 696, 852-8.

A Pérez-Rebolledo, GM de Lima, NL Speziali, OE Piro, EE Castellano, JD Ardisson and H Beraldo. Tin(IV) complexes obtained by reacting 2-benzoylpyridine-derived thiosemicarbazones with SnCl4 and Ph2SnCl2. J. Organomet. Chem. 2006; 691, 3919-30.

SR Batten. Structural and spectral studies of a new copper(II) complex with a tridentate thiosemicarbazone ligand. Struct. Chem. 2008; 9, 137-42.

H Keles, DM Emir and M Keles. A comparative study of the corrosion inhibition of low carbon steel in HCl solution by an imine compound and its cobalt complex. Corros. Sci. 2015; 101, 19-31.

NZN Hashim, K Kassim and Y Mohd. (E)-N1-(4-chlorobenzylidene)-N4-phenylbenzene-1,4-diamine as mild steel corrosion inhibitor in 1 M HCl. APCBEE Procedia. 2012; 3, 239-44.

KS Jacob and G Parameswaran. Corrosion inhibition of mild steel in hydrochloric acid solution by Schiff base furoin thiosemicarbazone. Corros. Sci. 2010; 52, 224-8.

FM Mahgoub and SM Al-Rashdi. Investigate the corrosion inhibition of mild steel in sulfuric acid solution by thiosemicarbazide. Open J. Phys. Chem. 2016; 6, 54-66.

TI Kashar, M Abdel-Motaal, K Emran and NA Sukar. Preparation and characterization of thiosemicarbazones corrosion inhibition effect and the antimicrobial and anticancer effect on their metal complexes. Eur. Sci. J. 2017; 13, 249-78.

B Xu, W Yang, Y Liu, X Yin, W Gong and Y Chen. Experimental and theoretical evaluation of two pyridinecarboxaldehyde thiosemicarbazone compounds as corrosion inhibitors for mild steel in hydrochloric acid solution. Corros. Sci. 2014; 78, 260-8.

DB Hmamou, R Salghi, A Zarrouk, H Zarrok, R Touzani, B Hammouti and AE Assyry. Investigation of corrosion inhibition of carbon steel in 0.5 M H2SO4 by new bipyrazole derivative using experimental and theoretical approaches. J. Environ. Chem. Eng. 2015; 3, 2031-41.

CG Dariva and AF Galio. Corrosion inhibitors - principles, mechanisms and applications. In: M Aliofkhazraei (Ed.). Developments in corrosion protection. IntechOpen, London, 2014, p. 710.

AM Al-Bonayan. Inhibiting effect of thiosemicarbazide and 4-phenyl thiosemicarbazide towards the corrosion of carbon steel in H3PO4 solutions. Int. J. Electrochem. Sci. 2015; 10, 589-601.

S Chitra, K Parameswari, C Sivakami and A Selvaraj. Sulpha Schiff bases as corrosion inhibitors for mild steel in 1 M sulphuric acid. Chem. Eng. Res. Bull. 2010; 14, 1-6.

M Prajila, J Sam, J Bincy and J Abraham. Electroanalytical studies on the interaction of 4-(N,N-dimethylaminobenzilidine)-3-mercapto-6-methyl-1, 2, 4-triazin (4H)-5-one (DAMMT) with mild steel in perchloric acid. J. Mater. Environ. Sci. 2012; 3, 1045-64.

C Verma, MA Quraishi, K Kluza, M Makowska-Janusik, LO Olasunkanmi and EE Ebenso. Corrosion inhibition of mild steel in 1 M HCl by D-glucose derivatives of dihydropyrido [2,3-d:6,5-d′] dipyrimidine-2, 4, 6, 8(1H,3H, 5H,7H)-tetraone. Sci. Rep. 2017; 7, 1-17.

H Zarrok, H Oudda and A Zarrouk. Weight loss measurement and theoretical study of new pyridazine compound as corrosion inhibitor for C38 steel in hydrochloric acid solution. Der Pharma Chem. 2011; 3, 576-90.

MR Vinutha and TV Venkatesha. Review on mechanistic action of inhibitors on steel corrosion in acidic media. Port. Electrochim. Acta 2016; 34, 157-84.

Z Zhan, M Sun, Y Jiang, L Li and J Li. Effect of tin on the corrosion resistance of 16 Cr ferritic stainless steel in acidic solution and chloride-containing media. Int. J. Electrochem. Sci. 2016; 11, 3963-75.

G Khan, WJ Basirun, SN Kazi, P Ahmed, L Magaji, SM Ahmed, GM Khan and MA Rehman. Electrochemical investigation on the corrosion inhibition of mild steel by quinazoline Schiff base compounds in hydrochloric acid solution. J. Colloid Interface Sci. 2017; 502, 134-45.

AAH Kadhum, AB Mohamad, LA Hammed, AA Al-Amiery, NH San and AY Musa. Inhibition of mild steel corrosion in hydrochloric acid solution by new coumarin. Mater. 2014; 7, 4335-48.

NK Mohd, MJ Ghazali, YS Kian, NA Ibrahim, WMZWS Yunus, MM Nor and Z Idris. Corrosion inhibitor of mild steel in hydrochloric acid solution using fatty acid derivatives. J. Oil Palm Res. 2017; 29, 97-109.

GE Badr. The role of some thiosemicarbazide derivatives as corrosion inhibitors for C-steel in acidic media. Corros. Sci. 2009; 51, 2529-36.

Downloads

Published

2022-06-09

How to Cite

Hazani, N. N. ., Dzulkifli, N. N. ., Ghazali, S. A. I. S. M. ., & Mohd, Y. . (2022). Synthesis, Characterisation and Corrosion Inhibition of Mild Steel by Butyltin(IV) 2-Acetylpyridine 4-Methyl-3-Thiosemicarbazone in HCl. Trends in Sciences, 19(12), 4615. https://doi.org/10.48048/tis.2022.4615

Most read articles by the same author(s)