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Corrosion inhibitors concentration

After increasing coolant corrosion-inhibitor concentration, coupon corrosion rates decreased by almost 70%. [Pg.91]

The common method of treating rod-pumped wells is to periodically batch inhibitor into them. The treatment period for a given well is selected using empirical rules based on well production volumes. A successful and economic corrosion inhibition program must carefully control the inhibitor concentration in the well fluids. Environmental aspects and efficacious inhibitor usage necessitate the measurement of very low corrosion inhibitor concentrations. Inhibitor concentrations as low as one part per million are significant, thus... [Pg.85]

Online passivation involves elevating the corrosion inhibitor concentration as high as three times normal maintenance levels. At higher concentrations, the rate at which the protective film forms is accelerated. This, in turn, reduces the degree of initial corrosion on clean but unprotected metal surfaces. The rate at which corrosion protection takes place depends on the temperature, pH and inhibitor used. [Pg.189]

The corresponding corrosion potential (Ecorr), corrosion current density (icon), anodic Tafel slope (ba), cathodic Tafel slope (be) and CR for uninhibited and inhibited systems from PP measurement are listed in Table 3. The data demonstrates that the Ecorr values shift to more positive values as the concentration of added studied inhibitors are increased. On the other hand, the corrosion current densities are markedly declined upon addition of the studied corrosion inhibitors. The extent of its decline increases with increasing of the corrosion inhibitor concentration. Moreover, the numerical values of both anodic and cathodic Tafel slopes decreased as the concentration of inhibitors were increased. This means that the three natural products have significant effects on retarding the anodic dissolution of aluminium alloy and inhibiting the cathodic hydrogen evolution reaction. [Pg.381]

The values of Ret and double layer capacitance, Cai for Al-Mg-Si alloy at various concentrations of NH, VL and TS are presented in Table 4. The results show that the Ret values increase with the addition of corrosion inhibitors when compared with those without corrosion inhibitor. Furthermore, the values of Ret are observed to increase with the increasing corrosion inhibitor concentration, which can be attributed to the formation of a protective over-layer at the metal surface. It becomes a barrier for the charge transfers. [Pg.383]

Note The recommended range for corrosion inhibitor concentration is 0.1%-2.0% (depending on temperature and metal),The recommended range for inhibitor-intensifier concentration depends on the type of agent (e,g iodide salts, 0,2%-3% formic acid, 0.5%-5%). Values given are for 24 hours of metal/acid contact time,... [Pg.84]

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. [Pg.186]

Metals. Most metals react with aqueous HCl foUowing equation 22. The reaction rate is dependent on the concentration of the acid, oxidi2ing, reducing, or complexing agents, and corrosion inhibitors, in addition to the metallurgical characteristics of the material and the prevailing hydrodynamic conditions (see Corrosion and corrosion control). [Pg.446]

Nitrate and Nitrite. Nitrate is usually present in trace quantities in surface waters but occasionally occurs in high concentrations in some groundwaters. If present in excessive amounts, it can contribute to the illness infant methemoglobinemia. Nitrate is an essential nutrient for many photosynthetic autotrophs. Nitrite is an intermediate in the reduction of nitrate as well as in the oxidation of ammonia it is also used as a corrosion inhibitor in some industrial processes. [Pg.231]

The freezing point of the coolant should be monitored for coolants in all types of service. Additionally, maintenance of the corrosion inhibitor levels is requited of the heavy-duty service coolants and the stationary engine coolants. Because corrosion inhibitors and combinations of corrosion inhibitors work most effectively at given concentrations and specific ratios to the other inhibitors, appropriate concentrations must be maintained to maximize corrosion protection. Many manufacturers of coolants for stationary engines, and manufacturers of SCAs, provide an analytical service to monitor the effective inhibitor concentrations in the system periodically. Recommendations can then be made for proper maintenance and inhibitor replenishment. [Pg.190]

Approximately 5% of the U.S. consumption of is in agriculture. Boron is a necessary trace nutrient for plants and is added in small quantities to a number of fertilizers. Borates are also used in crop sprays for fast rehef of boron deficiency. Borates, when apphed at relatively high concentration, act as nonselective herbicides. Small quantities of borates are used in the manufacture of alloys and refractories (qv). Molten borates readily dissolve other metal oxides usage as a flux in metallurgy is an important apphcation. Other important small volume apphcations for borates are in fire retardants for both plastics and ceUulosic materials, in hydrocarbon fuels for fungus control, and in automotive antifreeze for corrosion control (see Corrosion and corrosion inhibitors). Borates are used as neutron absorbers in nuclear reactors. Several borates, which are registered with the Environmental Protection Agency (EPA) can be used for insecticidal purposes, eg, TIM-BOR. [Pg.205]

Metal- Working and Hydraulic Fluids. In the preparation of fluids for metal-working and hydrauflcs, the trend has been to replace organic-based materials with aqueous-based materials. Neodecanoic acid has found apphcation in these newer fluids as a corrosion inhibitor and a viscosity improver. For example, neodecanoic acid is used in an aqueous hydrauflc fluid concentrate for corrosion inhibition and improved antiwear properties (101), in the preparation of a thickened aqueous hydrauflc fluid to reduce viscosity loss (102), and in a water-soluble metal working oil to reduce corrosion (103). In a similar vein, neodecanoic acid has been used in antifreeze concentrates for corrosion inhibition (104). [Pg.106]

Corrosion inhibitors are substances which slow down or prevent corrosion when added to an environment in which a metal usually corrodes. Corrosion inhibitors are usually added to a system in small amounts either continuously or intermittently. The effectiveness of corrosion inhibitors is partiy dependent on the metals or alloys to be protected as well as the severity of the environment. For example, the main factors which must be considered before apphcation of a corrosion inhibitor to an aqueous system are the compatibility of the inhibitor and the metal(s), the salt concentration, the pH, the dissolved oxygen concentration, and the concentration of interfering species such as chlorides or metal cations. In addition, many inhibitors, most notably chromates, are toxic and environmental regulations limit use. Attention is now being given to the development of more environmentally compatible inhibitors (37). [Pg.282]

Removing suspended solids, decreasing cycles of concentration, and clarification all may be beneficial in reducing deposits. Biodispersants and biocides should be used in biofouled systems. Simple pH adjustment may lessen precipitation of certain chemical species. The judicious use of chemical corrosion inhibitors has reduced virtually all forms of aqueous corrosion, including underdeposit corrosion. Of course, the cleaner the metal surface, the more effective most chemical inhibition will be. Process leaks must be identified and eliminated. [Pg.83]

Corrosion Inhibitors. An inhibitor is any substance that retards or slows down a chemical reaction. Thus, when added to the environment in small concentrations, inhibitors reduce the rate, or prevent the attack by the environment on the metal. The basic mechanisms by which inhibitors function are as follows [209] ... [Pg.1327]

Continuous Treatment. Continuous treatment involves introducing a corrosion inhibitor on a regular basis to maintain the specified concentrations of inhibitors in the system. Depending on the prevailing conditions and manufacturer s recommendation, the concentration may vary from a few parts per million to 50 ppm or more. [Pg.1331]

Whatever method of inhibitor application is used, care must be taken to maintain optimum concentration of the corrosion inhibitor. In the event of addition of makeup water or untreated reserve fluids to maintain other fluid properties, care must be taken to ensure the addition of the correct amounts of corrosion inhibitors. [Pg.1331]

Microbiocides may be toxic to humans therefore, care must be taken when used. When selecting the microbiocide, the field engineer can obtain pertinent information on chemicals from the service company providing the chemicals. The microbiocide selected must be compatible with the system in which it is being used. Some chemicals such as quaternary amines have dual functions one as microbiocides and the other as film-forming corrosion inhibitors. Insufficient concentrations of this type of chemical may not be enough to coat the whole surface of metal and can cause pitting corrosion. The selection must also depend on chemicals that can produce the desired control in minimum time limits and... [Pg.1335]

Dissolved mineral salts The principal ions found in water are calcium, magnesium, sodium, bicarbonate, sulphate, chloride and nitrate. A few parts per million of iron or manganese may sometimes be present and there may be traces of potassium salts, whose behaviour is very similar to that of sodium salts. From the corrosion point of view the small quantities of other acid radicals present, e.g. nitrite, phosphate, iodide, bromide and fluoride, have little significance. Larger concentrations of some of these ions, notably nitrite and phosphate, may act as corrosion inhibitors, but the small quantities present in natural waters will have little effect. Some of the minor constituents have other beneficial or harmful effects, e.g. there is an optimum concentration of fluoride for control of dental caries and very low iodide or high nitrate concentrations are objectionable on medical grounds. [Pg.354]

Another mineral constituent of water is silica, present both as a colloidal suspension and dissolved in the form of silicates. The concentration varies very widely and, as silicates are sometimes applied as corrosion inhibitors, it might be thought that the silica content would affect the corrosive properties of a water. In general, the effect appears to be trivial the fact that silicate inhibitors are used in waters with a high initial silica content suggests that the form in which silica is present is important. [Pg.356]

The atmospheric pollution prevailing in special industrial or laboratory locations may induce more severe corrosion, e.g. the vapours from concentrated hydrochloric or acetic acid will etch tin, and moist sulphur dioxide will produce a sulphide tarnish, as will hydrogen sulphide at temperatures above about 100°C. The halogens attack tin readily. The commonly used volatile corrosion inhibitors are without adverse action although the benefit derived from their use is doubtful. [Pg.804]

Maintenance of a correct inhibitor concentration (level) is particularly important where low-level treatments, e.g. less than 100 p.p.m. are used. Such treatments are, however, usually applied (for economic and effluent reasons) in large capacity systems, and plants of this nature will usually have skilled personnel available for control purposes. In smaller closed systems, e.g. automobile engines, higher concentrations of more than approximately 0-1% are commonly used, but in these applications there is usually a good reserve of inhibitor allowed for in the recommended concentration and routine checking is of less importance. Nevertheless, since these inhibitors are often of the dangerous type, gross depletion may lead to enhanced corrosion. [Pg.783]

Terminology The International Standards Organization has recently defined a corrosion inhibitor as a chemical substance which decreases the corrosion rate when present in the corrosion system at a suitable concentration, without significantly changing the concentration of any other corrosive agent. This last point is significant since it excludes chemicals employed for deaeration or pH control from the definition of a corrosion inhibitor. On the other hand, it should be noted that the inhibitor is .. . present in the corrosion system. . . , and thus arsenic when added to brasses to prevent dezin-cihcation may be classified as an inhibitor. [Pg.798]


See other pages where Corrosion inhibitors concentration is mentioned: [Pg.451]    [Pg.1013]    [Pg.457]    [Pg.83]    [Pg.83]    [Pg.451]    [Pg.1013]    [Pg.457]    [Pg.83]    [Pg.83]    [Pg.442]    [Pg.444]    [Pg.359]    [Pg.10]    [Pg.199]    [Pg.244]    [Pg.188]    [Pg.167]    [Pg.87]    [Pg.1326]    [Pg.1328]    [Pg.1331]    [Pg.1339]    [Pg.1342]    [Pg.20]    [Pg.337]    [Pg.777]    [Pg.783]    [Pg.786]    [Pg.787]    [Pg.795]    [Pg.812]   
See also in sourсe #XX -- [ Pg.1331 ]




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