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Buffers acid-base

How does a buffer solution maintain its pH at a nearly constant value Not only must the acid in the buffer react with added base and the base must react with added acid, but it is also necessary that the acid and base [Pg.196]

Buffer solution Solution of an acid plus a base that controls pH by reacting with added base or acid Buffer Combination of an acid and a base that can control pH [Pg.196]

Finding pH. To find the pH of a solution, it can be tested with an acid-base indicator, for example, (a) the natural indicator in a red cabbage solution, which (from left to right) has the colors shown for solutions of pH 1. 4, 7,10, and 13. (b) For a more accurate determination, an instrument known as a pH meter is used. [Pg.196]

Notice that in these reactions no new substances are produced. The products are always components of the buffer. Both acid and hase are neutralized hy different buffer components to maintain the pH at a constant value. [Pg.197]

Buffers are very important to many industrial and natural processes. In fact, the control of the pH of your blood is essential to your health. The pH of the blood is about 7.40, and your good health depends on the ability of buffers to maintain the pH within a narrow range. If the pH falls below 7.35, a condition known as acidosis occurs increasing pH above 7.45 leads to alkalosis. Both these conditions can be life threatening. [Pg.197]


A mixture of acetic acid and sodium acetate is one example of an acid/base buffer. The equilibrium position of the buffer is governed by the reaction... [Pg.168]

The relationship between the pH of an acid-base buffer and the relative amounts of CH3COOH and CH3COO- is derived by taking the negative log of both sides of equation 6.43 and solving for the pH... [Pg.168]

Acid-base buffers comprise both a weak acid or base and its respective salt. Calculations with buffers employing the Henderson-Hasselbach equation are introduced and evaluated, thereby allowing the calculation of the pH of a buffer. Next, titrations and pH indicators are discussed, and their modes of action placed into context. [Pg.233]

A buffer comprises (1) a weak acid and a salt of that acid, (2) a weak base and a salt of that base, or (3) it may contain an acid salt. We define an acid-base buffer as a solution whose pH does not change after adding (small amounts of) a strong acid or base . Sodium ascorbate is a favourite buffer in the food industry. [Pg.268]

The primary characteristic of an acid/base buffer affecting steam requirements is the temperature dependence of Pgc /P O-Since PSC /P O of the citrate system is independent of temperature, the ideal minimum steam requirement (moles H20/moles SO2) of a simple stripper is equal to the ratio, °f the... [Pg.284]

Zacharis, E., Moore, B.D. and Hailing, P.J., Control of enzyme activity in organic media by solid-state acid-base buffers. J. Am. Chem. Soc., 1997, 119, 12396-12397. [Pg.80]

Clay minerals are important to the crustal-ocean-atmosphere fectory, not just for their abundance, but because they participate in several biogeochemical processes. For example, the chemical weathering reactions responsible for their formation are accompanied by the uptake and release of cations and, thus, have a large impact on the chemical composition of river and seawater. This includes acid/base buffering reactions, making clay minerals responsible for the long-term control of the pH of seawater and, hence, of importance in regulating atmospheric CO2 levels. [Pg.351]

Equations 16-9 and 16-10 are analogous to the Henderson-Hasselbalch equation of acid-base buffers. Prior to the equivalence point, the redox titration is buffered to a potential near E+ = formal potential for Fc 1 Fe2+ by the presence of Fe 1 and Fe2+. After the equivalence point, the reaction is buffered to a potential near E+ = formal potential for Ce4+ Ce3+. [R. de Levie Redox Buffer Strength, J. Chem. Ed. 1999, 76, 574.]... [Pg.673]

Most companies producing ICs today have been quite lax in the quality control of the liquid chemicals used in their processes. These chemicals include acids, bases, buffered etches, photoresists, and organic solvents. Essentially, the producers of ICs have left the quality control of these materials to the chemical manufacturers. Specifications for chemicals are set by SEMI (Semiconductor Equipment Manufacturers International) and are generally met by all chemical manufacturers. The level of metallic contaminations that can exist in U.S. chemicals ranges from 0.1 to 1 ppm. If the levels of metallic impurities were actually this high, U.S. manufacturers would not be able to produce integrated circuits. [Pg.524]

Lucey, J. A., Gorry, C., and Fox, P. F. (1993). Changes in the acid-base buffering curves during the ripening of Emmental cheese. Milchwissenschaft 22, 224-231. [Pg.207]

The presence of acidic functional groups, mostly carboxyl and phenolic OH groups, in the molecular structure of soil HS renders them major players in the acid-base buffering capacity of soils and in the fate, bioavailability, and physico-chemical behavior of macro- and micronutrients, toxic metal ions, and several xenobiotic organic compounds in soil (Ritchie and Perdue, 2003 Senesi and Loffredo, 2005). Consequently, the effects of amendment on the acid-base properties of soil HAs and FAs is a subject of considerable interest. [Pg.154]

Conductivity detection is excellent for ionic or dipolar systems. It is optimal only if the ions under study are contained in solution or suspension, since the sensitivity of detection decreases when other electrolytes or acid-base buffers are added (Bernasconi, 1976). However, Strehlow and Wendt (1963) obtained good precision even in systems where 98% of the conductance was ascribable to inert electrolytes. One way to minimize extra conductance is to add salts with ions of low mobility such as tetra-alkylammonium ions, rather than sodium or potassium ions. [Pg.75]

Hartikainen H. 1996. Soil processes and chemical transport. Soil response to acid percolation Acid-base buffering and cation leaching. J Environ Qual 25 638-645. [Pg.322]

At the molecular level, the buffering capacity of the cellular solution may block the pollutant in its course. Pollutants that generate acids or bases may be neutralized by acid-base buffers. Excess calcium or other cations may complex fluoride, and redox systems may buffer S02, 03, or PAN, or the free radicals they generate. On another level, enzyme structure determines whether the pollutant will penetrate and react with an active site, and the functioning of an enzyme, apparently through effects on its structure, also modifies its susceptibility to the pollutant (6). Moreover, inhibition of a susceptible enzyme may not affect a pathway the enzyme affected may not be rate-limiting in a particular pathway, and considerably greater inhibition must occur before it is. [Pg.67]

Melton et al. [452] noticed that if NaCl is added to acidic A1C13-MEIC melts, it acts as a Lewis acid-base buffer. In these melts, NaCl reacts with A12C17 and a neutral salt results, as follows ... [Pg.573]

Phosphorus is an electrolyte (anion) in intracellular fluid that is converted by the body into phosphate. Phosphorus is involved in the function of red blood cells, muscles, the nervous system, acid-base buffering, and metabolizing carbohydrates, proteins, and fats. Phosphorus is mostly stored in bones, absorbed in the GI tract, and excreted in urine and a small amount in feces. [Pg.114]

There are compatibility issues for chromatographic methods and NMR. Protic solvents such as water or methanol are usually replaced with deuterated solvents although solvent suppression algorithms can be used with shallow gradient methods. Organic modifiers such as ion-pair reagents must be avoided, and mineral acid based buffer systems are preferred (the opposite of the LC-MS situation).34... [Pg.355]

Because the dissociation of acid-base pairs is an equilibrium reaction, the relationship between hydrogen ion concentration or pH and the relative concentrations of the acid and base can be described mathematically in terms of the dissociation constant for the acid-base buffer pair. When expressed as a logarithmic relationship, where pK is the negative logarithm of the dissociation constant this is known as the Henderson-Hasselbalch equation ... [Pg.984]

Dolman, M., Hailing, P. J., and Moore, B. D., Functionalized dendritic polyben-zylethers as acid/base buffers for biocatalysis in nonpolar solvents, Biotechnol. Bioeng., 55, 278-282, 1997. [Pg.224]

The redoxbuffer strength serves the same role for the potential of a solution as the acid-base buffer strength serves for its pH. In both cases it is assumed that the corresponding equilibria are established quickly on the time scale of the experiment. With redox equilibria, which often involve bond breaking, this condition is less often met than with acid-base equilibria, where fast establishment of equilibrium is the norm. [Pg.219]

Of course, if the hydrogen ion concentration changes, the extraction efficiency (D) will change. In this example, the hydrogen ion concentration will increase with increasing benzoic acid concentration, unless an acid-base buffer is added to maintain the hydrogen ion concentration constant (see Chapter 7 for a discussion of buffers). [Pg.543]

An acid-base buffer is a solution containing high concentrations of a... [Pg.615]

Consider just a few cases of aqueous equilibria. The magnificent formations i n limestone caves and the vast expanses of oceanic coral reefs result from subtle shifts in carbonate solubility equilibria. Carbonates also influence soil pH and prevent acidification of lakes by acid rain. Equilibria involving carbon dioxide and phosphates help organisms maintain cellular pH within narrow limits. Equilibria involving clays in soils control the availability of ionic nutrients for plants. The principles of ionic equilibrium also govern how water is softened, how substances are purified by precipitation of unwanted ions, and even how the weak acids in wine and vinegar influence the delicate taste of a fine French sauce. In this chapter, we explore three aqueous ionic equilibrium systems acid-base buffers, slightly soluble salts, and complex ions. [Pg.616]


See other pages where Buffers acid-base is mentioned: [Pg.171]    [Pg.171]    [Pg.171]    [Pg.177]    [Pg.115]    [Pg.319]    [Pg.322]    [Pg.15]    [Pg.45]    [Pg.36]    [Pg.413]    [Pg.730]    [Pg.730]    [Pg.789]    [Pg.218]    [Pg.283]    [Pg.400]    [Pg.235]    [Pg.252]    [Pg.253]    [Pg.255]    [Pg.265]    [Pg.615]    [Pg.616]    [Pg.616]   
See also in sourсe #XX -- [ Pg.196 , Pg.197 ]




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Acid) buffer

Acid-base balance buffers

Acid-base buffer strength

Acid-base buffer systems

Acid-base buffer systems Henderson-Hasselbalch equation

Acid-base buffer systems defined

Acid-base buffer systems described

Acid-base buffer systems preparing

Acid-base chemistry buffer solutions

Acid-base equilibria buffer solutions

Acid-base equilibria buffered solutions

Acid-base equilibrium problems with buffered solutions

Acid-base reactions buffer solutions

Acid-base reactions buffers

Acidic buffering

Acidic buffers

Acids and bases buffers

Acids buffering

Addition of Strong Acids or Bases to Buffers

Aqueous equilibria acid-base buffer systems

Base buffer

Buffer acid-base titration

Buffer capacity, acid-base

Buffer index, acid-base

Buffer mixture, acid-base

Buffer weak acid plus its salt with a strong base

Buffered acids

Equilibria of Acid-Base Buffer Systems

Equilibrium/equilibria Acid-base chemistry Buffers

Ionic equilibria acid-base buffer systems

Systems for Acid-Base Buffering

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