SYNTHESIS OF CORROSION INHIBITOR BASED ON MONOETHANOLAMINE AND PHOSPHATE ACID
1Ishonkulova GulxonTogaymuratovna, 2Beknazarov Khasan Soyibnazarovich,
3Ishankulova Mehri Muratovna
1Angren university, teacher, 2Angren university, DSc, professor, 3Angren university, teacher https://doi.org/10.5281/zenodo.11114076
Abstract. In this article, the optimal conditions for synthesizing corrosion inhibitors based on monoethanolamine, phosphoric acid, and formalin. The structure of this obtained corrosion inhibitor was analyzed by IR-spectra.
Keywords: monoethanolamine, phosphoric acid, formalin, corrosion inhibitor, IR-spectrum.
Introduction
The process of corrosion is a process of chemical and electrochemical as well as biological degradation of metals as a result of environmental effects [1,2]. According to the mechanism of the process, there is chemical, electrochemical, and biochemical corrosion. Corrosion begins at the surface of the metal and spreads deeper with further development of the process. The environment in which metal corrosion occurs is various liquids and gases [3,4]. Various amines, ketones, aliphatic carboxylic acids, and amino acids, as well as products of the interaction of amino alcohols and their derivatives with sulfonamides, carboxylic acids, ethers, and aldehydes, are used as organic inhibitors [5,6]. Amino acids such as glycine, methionine, and histidine glutamic acid are used as inhibitors against steel corrosion in sulfuric acid, aspartic acid in hydrochloric acid, alanine chloride, and sulfuric acid [7,8].
Experimental part
Materials
Monoethanolamine, Phosphoric acid and Formaldehyde are used to syntheses a new corrosion inhibitor . All chemical reagents: orthophosphoric acid, monoethanolamine, and formaldehyde were purchased "chemically pure" from "Merit Chemicals" company.
Methods. The structure of this synthesized corrosion inhibitor was carried out and analyzed on a SHIMADZU (IRAffinity-1S) device. The gravimetric method was used to determine the inhibition efficiency of the synthesized inhibitor.
Synthesis of MFP-1 brand corrosion inhibitor. It was carried out in a 250 cm3 round-bottomed flask equipped with a stirrer, a reflux condenser and a thermometer. First, monoethanolamine and phosphoric acid were mixed different ratio at a temperature of 65-70 0C for 15 minutes, then formalin was added dropwise and the temperature was increased to a temperature of 95-100 0C, and the reaction was stirred for 90 minutes. Reaction product. It is 88,9 % and it is a pale yellow and dark substance, which dissolves well in hot water.
Results and Discussion
IR spectroscopy analysis. According to the results of the IR spectrum of MFP-1, groups corresponding to absorption maxima in the following range are given: 2931-2819 cm-1 v (ON), 1635-1525 cm-1, v (-CONHR), 1458 cm-1 vs(-O- CH2-), vs(-N-C№), 1340 cm-1 vs(R=O), 1037 cm-1 v (P-O-C) (Fig. 2.1).
EU 8HIMADZU
M<MT1
r Si\ - 2 \ 9~ \ J
? K « I 5 s u /
/
a\ /
Su \
* s U, v £
5
Figure 2.1. IR spectrum image of MFP-1 brand corrosion inhibitor
According to the analysis of the IR spectrum of MFP-1, vibrational lines of the (OH) bound hydroxyl group appeared in the 2931-2819 cm-1 range, valence deformation vibration lines of the secondary amide group appeared in the v (-CONHR) range of 1635-1525 cm-1, and, vs(-O-CH2), vs(-N-CH2) groups in the 1458 cm-1 area, phosphorus oxygen bond in the 1340 cm-1 vs(R=O) area, 1111 cm-1 bond, absorption maxima corresponding to v (P-O-C) ether group at 1037 cm-1 were formed. According to the results of IR analysis, the formula of this substance can be said as follows [9].
Conclusion
In this research, the optimal conditions for the synthesis of MFP-1 brand corrosion inhibitor based on monoethanolamine, phosphoric acid, and formalin were determined. The structure of the synthesized corrosion inhibitor was analyzed using IR spectra. Also, its absorption efficiency in aqueous medium was 88,9 % when it was organized using the gravimetric method.
References
1. Nurilloev Zafar, Beknazarov Khasan and Nomozov Abror, "Production of Corrosion Inhibitors Based on Crotonaldehyde and Their Inhibitory Properties," International Journal of Engineering Trends and Technology., 2022, vol. 70, 8, pp. 423-434, Crossref, https://doi.org/10.14445/22315381/IJETT-V70I8P243.
2. Narzullaev A.X, Beknazarov X.S, Jalilov A.T and Rajabova M.F, "Studying the Efficiency of Corrosion Inhibitor IKTSF-1, IR-DEA, IR-DAR-20 in 1m HCl," International Journal of Advanced Science and Technology , vol. 28, no. 15, pp. 113-122. Available At:. http://sersc.org/journals/index.php/IJAST/article/view/1555.
3. Nomozov A.K et all. Study of processe of obtaining monopotassium phosphate based on monosodium phosphate and potassium chloride. Chemical Problems. 2023 no. 3 (21). DOI: 10.32737/2221-8688-2023-3-279-293.
4. Nomozov A, K, et.all. Salsola Oppositifolia acid extract as a green corrosion inhibitor for carbon steel. Indian Journal of Chemical Technology. 2023, 30, 872-877. https://doi.org/10.56042/ijct.v30i6.6553.
5. Beknazarov, K.S., Dzhalilov, A.T., Ostanov, U.Y., Erkaev, A.M. The inhibition of the corrosion of carbon steel by oligomeric corrosion inhibitors in different media. International Polymer Science and Technology.,2015, 42(4), pp. T33-T37.
6. Beknazarov Kh.S., Jalilov A.T. Comparative assessment of the effectiveness of antioxidants based on oligomeric derivatives of gossypol and Irganok-1010 in stabilizing polyethylene // Composite materials. 2013. No.2.69-73.
7. N.K. Gupta, M.A. Quraishi, C. Verma and A.K. Mukherjee, Green Schiffs bases as corrosion inhibitors for mild steel in 1 M HCl solution: experimental and theoretical approach, RSC Adv., 2016, 6, 102076-102087. doi: 10.1039/C6RA22116E.
8. M. Lagrenee, B. Mernari, M. Bouanis, M. Traisnel and F. Bentiss, Study of the mechanism and inhibiting efficiency of 3,5-bis(4-methylthiophenyl)-4H-1,2,4-triazole on mild steel corrosion in acidic media, Corros. Sci., 2002, 44, no. 3, 573-588. doi:10.1016/S0010-938X(01)00075-0.
9. N.K. Gupta, M.A. Quraishi, C. Verma and A.K. Mukherjee, Green Schiffs bases as corrosion inhibitors for mild steel in 1 M HCl solution: experimental and theoretical approach, RSC Adv., 2016, 6, 102076-102087. doi: 10.1039