Heteropolysaccharides in sustainable corrosion inhibition: 4E (Energy, Economy, Ecology, and Effectivity) dimensions

Carbohydrate polymers (polysaccharides) and their derivatives are widely utilized in sustainable corrosion inhibition (SCI) because of their various fascinating properties including multiple adsorption sites, high solubility and high efficiency. Contrary to traditional synthetic polymer-based corros...

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Published inInternational journal of biological macromolecules Vol. 235; p. 123571
Main Authors Ganjoo, Richika, Sharma, Shveta, Verma, Chandrabhan, Quraishi, M.A., Kumar, Ashish
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 30.04.2023
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Summary:Carbohydrate polymers (polysaccharides) and their derivatives are widely utilized in sustainable corrosion inhibition (SCI) because of their various fascinating properties including multiple adsorption sites, high solubility and high efficiency. Contrary to traditional synthetic polymer-based corrosion inhibitors, polysaccharides are related to the 4E dimension, which stands for Energy, Economy, Ecology, and Effectivity. Furthermore, they are relatively more environmentally benign, biodegradable, and non-bioaccumulative. The current review describes the SCI features of various heteropolysaccharides, including gum Arabic (GA), glycosaminoglycans (chondroitin-4-sulfate (CS), hyaluronic acid (HA), heparin, etc.), pectin, alginates, and agar for the first time. They demonstrate impressive anticorrosive activity for different metals and alloys in a variety of corrosive electrolytes. Through their adsorption at the metal/electrolyte interface, heteropolysaccharides function by producing a corrosion-protective film. In general, their adsorption follows the Langmuir isotherm model. In their molecular structures, heteropolysaccharides contain several polar functional groups like –OH, –NH2, –COCH3, –CH2OH, cyclic and bridging O, –CH2SO3H, –SO3OH, –COOH, –NHCOCH3, –OHOR, etc. that serve as adsorption centers when they bind to metallic surfaces. [Display omitted]
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
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ObjectType-Review-1
ISSN:0141-8130
1879-0003
DOI:10.1016/j.ijbiomac.2023.123571