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4H82J
The reactions of chlorazone with α-chloroethyl esters of n-C 8 H 17 OH, n-C 10 H 21 OH, n-C 12 H 25 OH, CH 3 -CH=CCl-CH 2 OH alcohols for the first time were carried out, and chlorazone esters containing two ROCH 2 groups of these esters were obtained. The reactions of N 1 -alkoxymethyl-N 3 -alkoxymethylguanidine compounds with these chlorazone esters were carried out and 4 new guanidine derivatives (conventionally designated as I-IV) were synthesized, not known in the literature. Studies have been conducted to establish corrosion inhibitory efficiency for each of the newly synthesized compounds of guanidine I-IV in a very strong aggressive environment created in the laboratory. It was established that the inhibitory effectiveness of these compounds in concentrations of 1.0; 2.0; 2.5 mg/l is 99.97-100%. A comparative study of the effective inhibitory properties of the new synthesized guanidine compounds for corrosion protection of steel “St.3” was carried out. Studies have shown that each of the new I-IV compounds of guanidine in terms of environmental safety, economic and environmental efficiency is 5-10 times higher than the inhibitors currently used to protect from corrosion steel processing equipment operating in aggressive environments.
S.R.Hajiyeva. 2020. \u201cSynthesis and Research of New Compounds of Guanidine on the Basis of α-Chlorether and Chlorazone\u201d. Global Journal of Science Frontier Research - B: Chemistry GJSFR-B Volume 20 (GJSFR Volume 20 Issue B2).
Crossref Journal DOI 10.17406/GJSFR
Print ISSN 0975-5896
e-ISSN 2249-4626
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Total Score: 108
Country: Azerbaijan
Subject: Global Journal of Science Frontier Research - B: Chemistry
Authors: S.R.Hajiyeva, G.I.Bayramov, F.Е.Huseynov, T.I.Aliyeva, H.L.Rafiyeva, Z.T.Valiyeva, A.A.Samadova, N.M.Jafarova (PhD/Dr. count: 0)
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Publish Date: 2020 09, Tue
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This study aims to comprehensively analyse the complex interplay between
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