Hydrochloric acid (HCl) may contain traces of impurities that will change the aggressiveness of the solution. This article discusses the effects of impurities such as fluorides, ferric salts, cupric salts, chlorine, and organic solvents, in HCl. It describes the corrosion resistance of various metals and alloys in HCl, including carbon and alloy steels, austenitic stainless steels, standard ferritic stainless steels, nickel and nickel alloys, copper and copper alloys, corrosion-resistant cast iron, zirconium, titanium and titanium alloys, tantalum and its alloys, and noble metals. The article illustrates the effect of HCl on nonmetallic materials such as natural rubber, neoprene, thermoplastics, and reinforced thermoset plastics. It also tabulates the corrosion of various metals in dry hydrogen chloride.

This article describes the methods used for coloring anodized aluminum coatings: integral coloring, electrolytic coloring, chemical coloring, and organic dyeing. It discusses organic dye chemistry in terms of single-component organic dyes and multicomponent dyes. The article reviews optimal dyeing conditions, such as temperature, time, concentration, and pH. It concludes with a discussion on the factors considered for choosing a coloring method: the desired shade, light fastness, heat fastness, and contamination.

For chemical processing, niobium resists a wide variety of corrosive environments, including mineral acids, many organic acids, liquid metals, and most salt solutions. This article focuses on the mechanisms of corrosion resistance of niobium alloys in these environments. The niobium alloys include Nb-1Zr, Nb-55Ti, Nb-50Ta, and Nb-40Ta. The article describes the use of these corrosion resistant niobium alloys, and provides information on applications of niobium in various industries.

Etching aluminum can be a pretreatment step for anodizing, chemical conversion coating, metal-to-rubber bonding, and a host of other processes. Chemical etching, using either alkaline or acid solutions, produces a matte finish on aluminum products. This article describes the alkaline etching and acid etching of aluminum. Alkaline etching reduces or eliminates surface scratches, nicks, extrusion die lines, and other imperfections. Acid etching can be done without heavy smut problems, particularly on aluminum die castings. Hydrochloric, hydrofluoric, nitric, phosphoric, chromic, and sulfuric acids are used in acid etching. The article presents a flow chart of the operations used in acid etching.

This article discusses the environmental factors and kinetics of atmospheric corrosion, aqueous corrosion, and soil corrosion of carbon steels. It also provides information on corrosion in concrete and steel boilers.

This article describes the eight chemical cleaning methods, namely, circulation, fill and soak, cascade, foam, vapor-phase organic, steam-injected, on-line chemical, and mechanical cleaning. It presents information on deposit types, solvents used to remove them, and construction material incompatibilities in a table. The article summarizes the uses of chemical cleaning solutions, including hydrochloric acid, phosphoric acid, and sulfamic acid, as well as the additives used to neutralize their impact on corrosion. It discusses the chemical cleaning procedures, including selection of cleaning method and solvent, documentation of cleaning, and corrosion monitoring in chemical cleaning.

Mixtures of acids or acids and salts are of great importance to the chemical process industry (CPI) for use in digestion of solids, as a promoter in reactions, as a scale remover, and as a complexant. This article emphasizes the assessment of the performance of Ni-Fe-Cr-Mo alloys in mixed acids and salts in an objective manner. It tabulates the nominal compositions of pertinent Ni-Fe-Cr-Mo corrosion-resistant alloys. The article describes the acid and acid-plus-salt mixtures classified into the following general categories: nonoxidizing acid mixtures (H 2 SO 4 +H 3 PO 4 ), nonoxidizing acids with halides (H 2 SO 4 +HCl), oxidizing acid mixtures without halides (H 2 SO 4 +HNO 3 ), and oxidizing acid mixtures with halides (HNO 3 +HF). It also illustrates the effect of alloying elements on the corrosion rate in the nonoxidizing mixtures and oxidizing acid mixtures.

This article reviews the corrosion behavior in various environments for seven important nickel alloy families: commercially pure nickel, Ni-Cu, Ni-Mo, Ni-Cr, Ni-Cr-Mo, Ni-Cr-Fe, and Ni-Fe-Cr. It examines the behavior of nickel alloys in corrosive media found in industrial settings. The corrosive media include: hydrochloric acid, sulfuric acid, phosphoric acid, hydrofluoric acid, hydrobromic acid, nitric acid, organic acids, salts, seawater, and alkalis. The modes of high-temperature corrosion include oxidation, carburization, metal dusting, sulfidation, nitridation, corrosion by halogens, and corrosion by molten salts. Applications where the corrosion properties of nickel alloys are important factors in materials selection include the petroleum, chemical, and electrical power industries. Most nickel alloys are much more resistant than the stainless steels to reducing acids, such as hydrochloric, and some are extremely resistant to the chloride-induced phenomena of pitting, crevice attack, and stress-corrosion cracking (to which the stainless steels are susceptible). Nickel alloys are also among the few metallic materials able to cope with hot hydrofluoric acid. The conditions where nickel alloys suffer environmentally assisted cracking are highly specific and therefore avoidable by proper design of the industrial components.

This article provides a description of the classification, industrial applications, microstructures, physical, chemical, corrosion, and mechanical properties of zirconium and its alloys. It discusses the formation of oxide films and the effects of water, temperature, and pH on zirconium. The delayed hydride cracking of zirconium is also described. The article provides information on the resistance of zirconium to various types of corrosion, including pitting corrosion, crevice corrosion, intergranular corrosion, galvanic corrosion, microbiologically induced corrosion, erosion-corrosion, and fretting corrosion. The article explains the effects of tin content in zirconium and effects of fabrication on corrosion. Corrosion control measures for all types of corrosion are also highlighted. The article concludes with information on the safety precautions associated with handling of zirconium.

Filiform corrosion has been observed to occur under a wide range of organic coatings and proceeds with the same general characteristics on steel, aluminum, and magnesium. This article describes the standard tests for filiform corrosion, characteristics and mechanisms of filiform corrosion in steels, as well as coated aluminum and magnesium. It concludes with information on the prevention and mitigation of filiform corrosion accomplished through the adjustment of the environment and changes in the substrate and coating systems.

Cast cobalt alloys were developed to bridge the gap between high-speed steels and carbides. Although comparable in room-temperature hardness to high-speed steel tools, cast cobalt alloy tools retain their hardness to a much higher temperature and can be used at higher cutting speeds than high-speed steel tools. This article provides an overview of the processing, properties, and applications of these alloys.

Surface treatments are applied to magnesium parts primarily to improve their appearance and corrosion resistance. Mechanical and chemical cleaning methods are used singly or in combination, depending on the specific application and product involved to ensure repetitive reliability. This article focuses on mechanical finishing methods, namely, barrel tumbling, polishing, buffing, vibratory finishing, fiber brushing, and shot blasting. It provides useful information on process control and difficulties with chemical and anodic treatments of magnesium alloys. The use and applications of plating and organic finishing of magnesium alloys are also reviewed. The article concludes with a description of health and safety precautions to be followed during the surface treatment process.

Soluble salts on a surface can affect a steel substrate or coating in two principal ways: corrosion acceleration and osmotic blistering. This article provides a detailed discussion on the mechanisms for each of these deleterious effects. It describes the most detrimental anions with regard to corrosion, namely, chlorides, sulfates, and nitrates, and provides information on recognition and testing of the presence of soluble salts. The salt-measurement techniques and commercially available equipment are also described. The article provides information on research regarding tolerable levels of salts beneath coatings. The information shows that there appears to be a threshold limit to the salt contamination that a given coating/coating system can tolerate in a given environment.

This article discusses the procedures used for pickling nickel and nickel alloys. Nickel alloys can be divided into four groups: high-nickel alloys, nickel-copper alloys, nickel-chromium alloys, and nickel-iron-chromium alloys. Alloys within each composition group that has similar surface conditions are pickled in the same solutions using the same procedures. The article discusses three different surface conditions for pickling these nickel alloys: bright annealed white surface requiring removal of tarnish by flash pickling; bright annealed oxidized surface requiring removal of a layer of reduced oxide, sometimes followed by a flash pickle to brighten; and black or dark-colored surface requiring removal of adherent oxide film or scale. The article also reviews specialized pickling operations of nickel alloys and various cleaning and finishing operations, including grinding, polishing, buffing, brushing, and blasting.

This article provides information on the compositions of alkaline and acid baths and process parameters for zinc-iron, zinc-cobalt, zinc-nickel, and tin-zinc plating.

Corrosion of metals is defined as deterioration caused by chemical or electrochemical reaction of the metal with its environment. This article provides information on corrosion of iron and steel by aqueous and nonaqueous media. It discusses the corrosive environments of carbon and alloy steels, namely atmospheric corrosion, soil corrosion, corrosion in fresh water and seawater. The article describes the corrosion process in concrete, which tends to create conditions that increase the rate of attack. The focus is on the stress-corrosion cracking of steels; an environmentally induced crack propagation that results from the combined interaction of mechanical stress and corrosion reactions. The article tabulates a guide on corrosion prevention for carbon steels in various environments. It also discusses protection methods of steel from corrosion, including coatings, such as temporary protection, cleaning, hot dip coating, electroplating, thermal spray coatings, conversion coatings, thin organic coatings, and inhibitors.

Organic acids represent a key group of industrial chemicals. This article provides information on the corrosion characteristics of organic acids. It focuses on corrosion caused by acetic, formic, and propionic acids on various metals and alloy groups. These include steel, aluminum, copper and its alloys, stainless steels, titanium, and nickel alloys. The article also provides information on longer-chain organic acids.

Molten salts, or fused salts, can cause corrosion by the solution of constituents of the container material, selective attack, pitting, electrochemical reactions, mass transport due to thermal gradients, and reaction of constituents and impurities of the molten salt with the container material. This article describes a test method performed using thermal convection loop for corrosion studies of molten salts. It discusses the purification of salts that are used in the Oak Ridge molten salt reactor experiment. The article also reviews the corrosion characteristics of nitrates/nitrites and fluoride salts with the aid of illustrations and equations.

The rate and form of corrosion that occur in a particular situation depend on many complex variables. This article discusses the rate of corrosion of lead in natural and domestic water depending on the degree of water hardness caused by calcium and magnesium salts. Lead exhibits consistent durability in all types of atmospheric exposure, including industrial, rural, and marine. The article tabulates the corrosion of lead in various natural outdoor atmospheres and the corrosion of lead alloys in various soils. It explains the factors that influence in initiating or accelerating corrosion: galvanic coupling, differential aeration, alkalinity, and stray currents. The resistance of lead and lead alloys to corrosion by a wide variety of chemicals is attributed to the polarization of local anodes caused by the formation of a relatively insoluble surface film of lead corrosion products. The article also provides information on the corrosion rate of lead in chemical environments.

Tantalum is one of the most versatile corrosion-resistant metals known. The outstanding corrosion resistance and inertness of tantalum are attributed to a very thin, impervious, protective oxide film that forms on exposure of the metal to slightly anodic or oxidizing conditions. This article provides a discussion on the mechanism of corrosion resistance and on the behavior of tantalum in different corrosive environments, namely, acids; salts; organic compounds; reagents, foods, and pharmaceuticals; body fluids and tissues; and gases. It contains several tables that summarize the effects of acids, salts, and miscellaneous corrosive reagents on tantalum and applications for tantalum equipment in chemical, pharmaceutical, and other industries. Finally, the article presents a discussion on hydrogen embrittlement, the galvanic effects, and cathodic protection of tantalum and describes the corrosion resistance of different types of tantalum-base alloys.