{"id":161341,"date":"2026-01-22T09:13:50","date_gmt":"2026-01-22T08:13:50","guid":{"rendered":"https:\/\/stalesia.com\/types-and-forms-of-corrosion\/"},"modified":"2026-10-01T14:43:45","modified_gmt":"2026-10-01T12:43:45","slug":"types-and-forms-of-corrosion","status":"publish","type":"post","link":"https:\/\/stalesia.com\/en\/knowledge-base\/types-and-forms-of-corrosion\/","title":{"rendered":"Types and Forms of Corrosion"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\"><strong>Corrosion<\/strong> is a physicochemical interaction between a metal and its environment. This interaction results in changes in the properties of the metal (e.g. stainless steel), which may lead to significant impairment of the function of the metal, the environment or the technical system of which they are part. Corrosion phenomena are most often classified by mechanism, type of corrosion damage, environment and occurrence in a given branch of industry.<br\/>Corrosion is the natural enemy of metals. Ordinary carbon steel reacts with oxygen in the air, which causes a layer of iron oxide to form on the steel surface. This layer is porous and allows further oxidation of the steel, causing corrosion that results in rust. In other words, corrosion is the gradual deterioration of metallic and non-metallic materials under the chemical and electrochemical action of the environment, as a result of which the condition and properties of the affected material change.<\/p>\n\n<p class=\"wp-block-paragraph\"><strong>Bimetallic corrosion<\/strong>, also known as galvanic corrosion, is corrosion caused by a corrosion cell in which the components of the installation, e.g. the electrodes, are two different metals. If two different metals are in an electrolyte, this allows an electric current to flow from the less noble metal (the anode) to the more noble metal (the cathode), and the anodic metal will corrode faster than if the metals were not in contact. In electrochemical couples, stainless steels usually act as the cathodic material, so in such a joint it is usually the other metal that is exposed to corrosion.<\/p>\n\n<p class=\"wp-block-paragraph\"><strong>Erosion corrosion<\/strong> \u2013 a process in which corrosion and erosion occur simultaneously \u2013 surface, mechanical wear of the material, e.g. by flowing liquids or gases containing fine solid particles. In stainless steel installations, erosion corrosion often occurs where the cross-section or the direction of flow of the medium changes. Erosion corrosion also depends closely on the flow velocity of the medium in the installation.<\/p>\n\n<p class=\"wp-block-paragraph\"><strong>Localised corrosion<\/strong> occurs locally on the surface of a metal exposed to a corrosive environment. Corrosion-resistant steels may be subject to various types of localised corrosion, such as pitting, crevice corrosion, intergranular corrosion and stress corrosion.<\/p>\n\n<p class=\"wp-block-paragraph\"><strong>Intergranular corrosion<\/strong> occurs when a solution attacks the grain boundaries without affecting the grain interiors. In other words, it is the selective dissolution of grain boundaries or adjacent areas as a result of a corrosion process. The factor initiating this process is the potential difference between the grain boundary depleted of Cr (chromium) in the case of chromium carbides \u2013 the anode \u2013 and an inclusion, intermetallic phase or impurities forming at the grain boundary. It depends on the chemical composition and heat treatment. This corrosion progresses from the surface into the metal. Strength and ductility then decrease sharply. A sample of material affected by this corrosion does not give a metallic ring and cracks during bending tests. In extreme cases it may crumble into powder. This type of corrosion is very dangerous. Determining exactly how far it has progressed is very difficult. It is assessed by microscopic examination and by measuring the increase in electrical resistance.<\/p>\n\n<p class=\"wp-block-paragraph\"><strong>Stress corrosion<\/strong> (stress corrosion cracking, season cracking) \u2013 localised corrosion occurring in a material subject to constant residual (manufacturing) or service stresses. Stress corrosion results from the combined action of an aggressive environment and mechanical stresses on materials susceptible to this type of corrosion. Stress corrosion causes cracking of metal (e.g. steel, brass or aluminium) or polymer components. Corrosion of metals is electrochemical in nature.<br\/>Stress corrosion occurs mainly in relatively mildly aggressive solutions, mainly chlorides (also bromides and iodides).<br\/>Stress corrosion cracking of alloys may be caused by factors such as: brasses \u2013 corrode in an atmosphere of ammonia or sulphur dioxide; carbon steels \u2013 corrode in alkaline environments and in the presence of nitrates; aluminium and magnesium alloys and chromium-nickel steels \u2013 corrode in the presence of chlorides<br\/>The stresses may be caused by external forces as well as residual stresses induced, for example, by cold working (drawing) or welding. A material under load and exposed to a corrosive environment is considered to be less resistant to that environment than an unloaded material. As a result of stresses, the metal surface is not energetically uniform. Higher-energy sites are formed, from which metal ions on the surface pass into solution more easily than from a defect-free surface. The defective surface becomes the negative pole and the defect-free surface the positive pole of the cell. In a corrosion cell, oxidation (electrochemical corrosion) takes place at the anode. The cracks run perpendicular to the principal stresses and may run along the grain boundaries (intergranular stress corrosion cracking) or through the grains (transgranular stress corrosion cracking).<br\/>Stress corrosion cracking is explained by the uneven distribution of alloy constituents, especially when they differ in chemical activity (e.g. zinc and copper in brasses). In brasses, stress corrosion cracks form at sites with a locally higher concentration of zinc atoms. For this reason, brasses containing up to 20% zinc (e.g. tombac) are the most resistant to this type of corrosion.<\/p>\n\n<p class=\"wp-block-paragraph\"><strong>Uniform corrosion<\/strong> is corrosion that occurs evenly over the entire surface of a metal in a corrosive environment. This type of corrosion reduces the mechanical properties of the material through a uniform reduction of the cross-section and loss of mass, and consequently lowers the strength properties of the corroded component. Uniform corrosion of corrosion-resistant steels is observed when the steel is in the active state, when the passive layer is unstable.<\/p>\n\n<p class=\"wp-block-paragraph\"><strong>Crevice corrosion<\/strong> \u2013 electrochemical localised corrosion that develops in places that are difficult to access. Joints between components in which the joined surfaces are not fused, e.g. bolted and riveted joints, are exposed to it. Crevice corrosion begins once the oxygen in the poorly accessible surroundings of the crevice has been used up. The process results in poorly soluble compounds being deposited at the mouth of the crevice and readily soluble salts inside it \u2013 acidifying the corrosive environment in the crevice.<\/p>\n\n<p class=\"wp-block-paragraph\"><strong>Pitting corrosion<\/strong> is localised corrosion that causes the formation of pits \u2013 cavities progressing from the surface into the steel. Pitting corrosion of corrosion-resistant steels consists in the formation of pits initiated where the passive oxide layer has been damaged, which may lead to complete perforation of thin-walled products. The main factors affecting the pitting resistance of stainless steels include the surface condition of the material (low surface roughness is beneficial) and the main alloying elements such as chromium, molybdenum and nickel.<\/p>\n\n<p class=\"wp-block-paragraph\"><strong>Passive layer<\/strong> \u2013 a thin, non-porous, stable and impermeable layer of oxides, mainly chromium oxides, covering the entire component and forming on the surface of corrosion-resistant (stainless) steel as a result of oxygen from the air or water combining with the chromium contained in the alloy. The passive layer on stainless steels tends to rebuild itself spontaneously in an oxygen-containing environment. This layer protects corrosion-resistant steel against naturally occurring corrosive agents.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Corrosion is a physicochemical interaction between a metal and its environment. This interaction results in changes in the properties of the metal (e.g. stainless steel), which may lead to significant impairment of the function of the metal, the environment or the technical system of which they are part. Corrosion phenomena are most often classified by [&hellip;]<\/p>\n","protected":false},"author":5,"featured_media":42763,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[2295],"tags":[],"class_list":["post-161341","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-materials"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Types and Forms of Corrosion<\/title>\n<meta name=\"description\" content=\"Learn more about Types and Forms of Corrosion in the Stalesia knowledge base.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/stalesia.com\/en\/knowledge-base\/types-and-forms-of-corrosion\/\" \/>\n<meta property=\"og:locale\" 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