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Carbon dioxide/carbonic acid system

The chemistry of the carbonic acid system in seawater has been one of the more intensely studied areas of carbonate geochemistry. This is because a very precise and detailed knowledge of this system is necessary to understand carbon dioxide cycling and the deposition of carbonate sediments in the marine environment. A major concept applicable to problems dealing with the behavior of carbonic acid and carbonate minerals in seawater is the idea of a constant ionic medium. This concept is based on the observation that the salt in seawater has almost constant composition, i.e., the ratios of the major ions are the same from place to place in the ocean (Marcet s principle). Possible exceptions can include seawater in evaporative lagoons, pores of marine sediments, and near river mouths. Consequently, the major ion composition of seawater can generally be determined from its salinity. It has been possible, therefore, to develop equations in which the influence of seawater composition on carbonate equilibria is described simply in terms of salinity. [Pg.3535]

Wachter, E. A. J. M. Hayes, 1985. Exchange of oxygen isotopes in carbon-dioxide-phosphoric acid systems. Chem. Geol. (Isot. Geosci. Sect.) 52 365-374. [Pg.371]

Carbon dioxide used in pH control or other wet service will form carbonic acid. Systems handling aqueous carbon dioxide should be fabricated from acid-resistant materials such as stainless steel. See CGA G-6.1 for more information [4]. [Pg.305]

Protonated and diprotonated carbonic acid and carbon dioxide may also have implications in biological carboxylation processes. Although behavior in highly acidic solvent systems cannot be extrapolated to in vivo conditions, related multidentate interactions at enzymatic sites are possible. [Pg.197]

In the course of mixture separation, the composition and properties of both mobile phase (MP) and stationary phase (SP) are purposefully altered by means of introduction of some active components into the MP, which are absorbed by it and then sorbed by the SP (e.g. on a silica gel layer). This procedure enables a new principle of control over chromatographic process to be implemented, which enhances the selectivity of separation. As a possible way of controlling the chromatographic system s properties in TLC, the pH of the mobile phase and sorbent surface may be changed by means of partial air replacement by ammonia (a basic gaseous component) or carbon dioxide (an acidic one). [Pg.99]

The scrubbing liquid must be chosen with specific reference to the gas being removed. The gas solubility in the liquid solvent should be high so that reasonable quantities of solvent are required. The solvent should have a low vapor pressure to reduce losses, be noncorrosive, inexpensive, nontoxic, nonflammable, chemically stable, and have a low freezing point. It is no wonder that water is the most popular solvent used in absorption devices. The water may be treated with an acid or a base to enhance removal of a specific gas. If carbon dioxide is present in the gaseous effluent and water is used as the scrubbing liquid, a solution of carbonic acid will gradually replace the water in the system. [Pg.478]

Both iron- and copper-based alloys are corroded more easily on either side of the neutral pH band. In low pH conditions e.g. due to carbon dioxide, the acidic environments attack the alloys readily, causing damage both at the points of initial corrosion and perhaps, consequentially, further along the system, by screening the surface with corrosion products and permitting the development of differential aeration cells. [Pg.843]

Hindered rotation, 33, 34 internal, 367 Homopolymer, 168, 183 Hot bands, 374 Hot lattice, 4, 11, 21 Hydrates, 7, 9, 21, 31, 41 crystallization, 44 Hydrochloric acid clathrates, 2 in hydroquinone, 7 Hydrogen, bound, 4, 175 bromine hydrate, 35 4- carbon dioxide system, 110 4 carbon monoxide system, 96, 108 chloride hydrate, 35 clathrates, 2 chloride, 30... [Pg.407]

Carbon dioxide, which damages condensate return systems via the formation of carbonic acid. [Pg.102]

These factors severely enhance the risks of condensate system corrosion by carbonic acid (resulting from a breakdown of the alkalinity in the boiler water and carbon dioxide [C02] carryover into the steam) and BW carryover. In addition, boiler operation is more difficult because the possible COC is severely limited, there-... [Pg.194]

In steam-condensate systems, we are primarily concerned with the effect of carbon dioxide on pH levels. For example (and assuming all carbon dioxide is fully hydrated to carbonic acid) ... [Pg.521]

In the human body, carbon dioxide provides the buffer. This is called the carbonic acid-hydrogen carbonate ion buffer system. This buffer system maintains the body s blood pH within acceptable levels. The main threat to the bloods pH is excess hydrogen ions produced by various chemical reactions in the body. When hydrogen ions are produced, hydrogen carbonate ions in the blood pick them up and convert them to carbonic acid ... [Pg.79]

The circulatory system carries out many important functions that contribute to homeostasis. It obtains oxygen from the lungs nutrients from the gastrointestinal tract and hormones from the endocrine glands and it delivers these substances to the tissues that need them. Furthermore, it removes metabolic waste products, such as carbon dioxide, lactic acid, and urea, from the tissues. Finally, it contributes to the actions of the immune system by transporting antibodies and leukocytes to areas of infection. Overall, the circulatory system plays a vital role in maintenance of optimal conditions for cell and tissue function. [Pg.194]

Carbon dioxide-water systems play an important role in controlling the pH of alkaline and calcareous soils as well as adjusting solubility of most trace elements and their compounds. Carbon dioxide dissolves in water to form dissolved C02 and dissociated carbonic acid, H2CO30 ... [Pg.77]

G. Prakash, G. K. S. Efficient Chemoselective Carboxylation of Aromatics to Arylcarboxylic Acids with Superelectrophilically Activated Carbon Dioxide-Al2CI6/Al System. J. Am. Chem. Soc. 2002, 124, 11379-11391. (d) Klumpp, D. A. Rendy, R. McElrea, A. Superacid Catalyzed Ring-opening Reactions Involving 2-Oxazolines and the Role of Superelectrophilic Intermediates. Tetrahedron Lett. 2004, 45, 7959-7961. [Pg.171]

Most of the available water content charts are applicable only to sweet lean natural gases, Moore, et al, (15) have developed a set of charts which are based on the Heidemann (8, 12) version of the SRK water prediction. The system used in this study contains nearly 6.0% carbon dioxide. The acid gases cause increased water solubility in the vapor phase. Our calculations simply verify these observations. [Pg.347]

The principal buffer system in blood serum is based on the equilibrium between carbonic acid, H2C03(aq), and the hydrogen carbonate ion, HCO3 . Carbonic acid is unstable, however. It is also in equilibrium with carbon dioxide. Therefore, a second equilibrium reaction is involved in the hydrogen carbonate buffer system in the blood the reaction between carbon dioxide and water to produce carbonic acid, and its reverse. The two equilibrium reactions are summarized below. [Pg.568]

The human body is a remarkable machine. It relies on a variety of safeguards to keep blood pH constant. Our blood constitutes a buffer system — meaning, it has components that can react with excess base or excess acid. Carbon dioxide, which is produced by the metabolism of food, dissolves in blood to produce carbonic acid, and carbonic acid can neutralize any excess base. The bicarbonate ion, also present in blood, will promptly take care of any surplus acid. The level of carbon dioxide in the blood adjusts to a body s rate of respiration. If blood pH drops — which actually means that the blood has... [Pg.295]

This buffer system is more complex than other conjugate acid-base pairs because one of its components, carbonic acid (H2C03), is formed from dissolved (d) carbon dioxide and water, in a reversible reaction ... [Pg.68]

As rainwater falls, it absorbs atmospheric carbon dioxide. Once in the rainwater, the carbon dioxide reacts with water to form an acid known as carbonic acid, H2C03, which, as we discuss in this chapter, makes rainwater naturally acidic. As the rainwater passes through the ground, the carbonic acid reacts with various basic minerals, such as limestone, to form products that are water soluble and thus carried away by the underground flow of water. This washing-away action over the course of millions of years creates caves.The world s most extensive cave system is in western Kentucky in Mammoth Cave National Park, where more than 300 miles of networked caves have been mapped. [Pg.329]

When dissolved in a solvent, some solutes combine with the solvent to form solvated species. The two outstanding examples in aqueous solution are carbon dioxide to form COz(aq) (carbonic acid) and ammonia to form NH3(aq) (ammonium hydroxide). In many cases the equilibrium constant for the reaction is unknown or not known with sufficient accuracy for thermodynamic purposes. Conventions have been established for treating such systems thermodynamically. Here we discuss the carbon dioxide-water... [Pg.302]

On the whole, when synthesizing a global model of the C02 biogeochemical cycle, the unit to simulate that part of the cycle spent in the ocean must describe how the ocean carbonate system works. Alekseev et al. (1992), analyzing the system C02 IICO, COj and the distribution of pH values in ocean waters, discovered that more than 80% of dissolved carbon dioxide is in the form of hydrocarbonate ion of HC03. This means that when synthesizing a model of the ocean carbonate system only the first stage of the dissociation of carbonic acid can be reliably considered. As a result, the flux of C02 dissolved in the upper layer of the ocean can be calculated by the formula... [Pg.168]

In January and March of 1988, Radian Corporation made a comprehensive series of performance measurements on the air pollution control system at Modesto (47). As shown in Table 12, the measurements included chlorinated dibenzo-p-dioxins (CDD), chlorinated dibenzofurans (CDF), polycyclic aromatic hydrocarbons (PAH), polychlorinated biphenols (PCB), total hydrocarbons (THC), ammonia, NOx, sulfur trioxide, sulfur dioxide, hydrochloric acid, carbon monoxide, and particulate matter. [Pg.55]


See other pages where Carbon dioxide/carbonic acid system is mentioned: [Pg.400]    [Pg.276]    [Pg.1]    [Pg.26]    [Pg.400]    [Pg.199]    [Pg.18]    [Pg.382]    [Pg.159]    [Pg.19]    [Pg.16]    [Pg.378]    [Pg.325]    [Pg.242]    [Pg.288]    [Pg.322]    [Pg.70]    [Pg.763]    [Pg.766]    [Pg.105]    [Pg.18]    [Pg.450]    [Pg.165]    [Pg.38]    [Pg.267]    [Pg.358]    [Pg.551]   
See also in sourсe #XX -- [ Pg.398 ]




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Carbon dioxide systems

Carbon system

Carbonate systems

Carbonic acid system

Dioxide Systems

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