Group corrosion

Pushkarev, Yu., and Figovsky, O. Protective Vulcanized Coatings on the Base of Oligobutadienes without Functional Groups, Corrosion Reviews 7, no. 1 (1999) 33-46. 

Crevice corrosion Stress corrosion cracking Intergranular corrosion Selective leaching Erosion corrosion Flydrogen damage Dilon [12] grouped corrosion into two categories. 

NACE CORROSION NETWORK (2002) Discussion Group Corrosion within offshore jacket legs... 

Stainless steel. A group of Cr or Cr —Ni steels showing an unusually high resistance to corrosion by the atmosphere and many chemical reagents. In order to achieve this resistance to corrosion > 12% Cr is necessary. 

Of the general formula, R - S — H, where R represents an aliphatic or cyclic radical, the thiols —also known as mercaptans— are acidic in behavior owing to their S—H functional group they are corrosive and malodorous. Their concentration in crude oils is very low if not zero, but they are created from other sulfur compounds during refining operations and show up in the light cuts, as illustrated in Table 8.6. 

Corrosion suppression by inhibitors can be achieved by adding chemical species to tlie environment, which lead to a strong reduction of tlie dissolution rate. Depending on tlieir specific action, corrosion inliibitors can be divided into tlie following groups. 

These fibers may find use in controUed release of dmgs, bactericides, and corrosion prevention chemicals (103). Fibers with different active groups have been made for sorption of chemicals. These fibers are designed to replace granular sorbents for air purification, for example, in air filtration masks (104). 

AH corrosion inhibitors in use as of this writing are oil-soluble surfactants (qv) which consist of a hydrophobic hydrocarbon backbone and a hydrophilic functional group. Oil-soluble surfactant-type additives were first used in 1946 by the Sinclair Oil Co. (38). Most corrosion inhibitors are carboxyhc acids (qv), amines, or amine salts (39), depending on the types of water bottoms encountered in the whole distribution system. The wrong choice of inhibitors can lead to unwanted reactions. Eor instance, use of an acidic corrosion inhibitor when the water bottoms are caustic can result in the formation of insoluble salts that can plug filters in the distribution system or in customers vehicles. Because these additives form a strongly adsorbed impervious film at the metal Hquid interface, low Hquid concentrations are usually adequate. Concentrations typically range up to 5 ppm. In many situations, pipeline companies add their own corrosion inhibitors on top of that added by refiners. 

Chromium is the most effective addition to improve the resistance of steels to corrosion and oxidation at elevated temperatures, and the chromium—molybdenum steels are an important class of alloys for use in steam (qv) power plants, petroleum (qv) refineries, and chemical-process equipment. The chromium content in these steels varies from 0.5 to 10%. As a group, the low carbon chromium—molybdenum steels have similar creep—mpture strengths, regardless of the chromium content, but corrosion and oxidation resistance increase progressively with chromium content. 

Standard Wrought Steels. Steels containing 11% and more of chromium are classed as stainless steels. The prime characteristics are corrosion and oxidation resistance, which increase as the chromium content is increased. Three groups of wrought stainless steels, series 200, 300, and 400, have composition limits that have been standardized by the American Iron and Steel Institute (AlSl) (see Steel). Figure 8 compares the creep—mpture strengths of the standard austenitic stainless steels that are most commonly used at elevated temperatures (35). Compositions of these steels are Hsted in Table 3. 

Shipment of hydrazine solutions is regulated in the United States by the Department of Transportation (DOT) which classifies all aqueous solutions between 64.4 and 37% N2H4 as "Corrosive" materials with a subsidiary risk of "Poison". Hydrazine has been identified by both the Environmental Protection Agency and the DOT as a hazardous material and has been assigned a reportable quantity (RQ) of 0.450 kg (1 lb) if spilled. Dmms for the shipment of these solutions must bear both the DOT specification "Corrosive" and "Poison" labels in association with the markings "RQ Hydrazine Aqueous Solution UN 2030." Aqueous solutions of 37% concentration or less are a hazard Class 6.1, UN 3293, Packing Group III and require "Keep Away From Food" placards and labels. 

Lubrication oil additives represent another important market segment for maleic anhydride derivatives. The molecular stmctures of importance are adducts of polyalkenyl succinic anhydrides (see Lubrication and lubricants). These materials act as dispersants and corrosion inhibitors (see Dispersants Corrosion and corrosion control). One particularly important polyalkenyl succinic anhydride molecule in this market is polyisobutylene succinic anhydride (PIBSA) where the polyisobutylene group has a molecular weight of 900 to 1500. Other polyalkenes are also used. Polyalkenyl succinic anhydride is further derivatized with various amines to produce both dispersants and corrosion inhibitors. Another type of dispersant is a polyester produced from a polyalkenyl succinic anhydride and pentaerythritol [115-77-5]. 

Zinc phosphate, Zn2(P0 2> forms the basis of a group of dental cements. Chromium and zinc phosphates are utilized in some metal-treating appHcations to provide corrosion protection and improved paint adhesion. Cobalt(II) phosphate octahydrate [10294-50-5] Co2(P0 2 8H20, is a lavender-colored substance used as a pigment in certain paints and ceramics. Copper phosphates exhibit bioactivity and are used as insecticides and fungicides. Zinc, lead, and silver phosphates are utilized in the production of specialty glasses. The phosphate salts of heavy metals such as Pb, Cr, and Cu, are extremely water insoluble. 

Table 3. Corrosion Resistance of Platinum-Group Metals ...

These oxazolines have cationic surface-active properties and are emulsifying agents of the water-in-oil type. They ate acid acceptors and, in some cases, corrosion inhibitors (see Corrosion). Reaction to oxazoline also is useful as a tool for determination of double-bond location in fatty acids (2), or for use as a protective group in synthesis (3). The oxazolines from AEPD and TRIS AMINO contain hydroxyl groups that can be esterified easily, giving waxes (qv) with saturated acids and drying oils (qv) with unsaturated acids. 

There is a health benefit associated with hindering hydrogen bonding. Alkylphenols as a class are generally regarded as corrosive health hazards, but this corrosivity is eliminated when the hydroxyl group is flanked by bulky substituents in the ortho positions. In fact, hindered phenols as a class of compounds are utilized as antioxidants in plastics with FDA approval for indirect food contact. 

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