Hydrogen acid concentration

By far the most widely known classes of pH-sensitive materials are the classes of chemical compounds that iaclude the acids, bases, and iadicators. The most interesting of these are the iadicators. These materials change colors as a function of pH and usually are totally reversible (see Hydrogen-ION concentration). 

Only acids are sour. Sourness is not identical to chemical acidity or pH, which is a function of the hydrogen ion concentration, but also appears to be a function of the entire acid molecule. A combination of pH and acid concentration determines the actual degree of the sour taste. At the same pH, any organic acid, eg, citric acid, exhibits a far greater sourness than a mineral acid, eg, hydrochloric acid (27,28). 

The specific heat of aqueous solutions of hydrogen chloride decreases with acid concentration (Fig. 4). The electrical conductivity of aqueous hydrogen chloride increases with temperature. Equivalent conductivity of these solutions ate summarized in Table 8. Other physicochemical data related to... 

Nickel-based aUoys have superior corrosion resistance to Hon-based aUoys. The only aUoys recommended for hot hydrochloric acid use are Ni—Mo aUoys containing 60—70% Ni and 25—33% Mo. Chlorimet (63 Ni, 32 Mo, 3 Fe) and HasteUoy (60 Ni, 28 Mo, 6 Fe) are found to be stable at aU acid concentrations in the absence of aH and Hon chlorides. Electroless nickel, a Ni—P aUoy containing 2—10% P, shows exceUent resistance to hot hydrogen chloride (71). The corrosion resistance increases with phosphoms content. This coating can be deposited on cast Hon, wrought Hon, mild steel, stainless steels, brass, bron2e, and aluminum (qv). 

A particular concentration measure of acidity of aqueous solutions is pH which usually is regarded as the common logarithm of the reciprocal of the hydrogen-ion concentration (see Hydrogen-ION activity). More precisely, the potential difference of the hydrogen electrode in normal acid and in normal alkah solution (—0.828 V at 25°C) is divided into 14 equal parts or pH units each pH unit is 0.0591 V. Operationally, pH is defined by pH = pH(soln) + E/K, where E is the emf of the cell ... 

A mathematical model of the operating characteristics of a modem HLW storage tank has been developed (60). This model correlates experimental data for the rate of radiolytic destmction of nitric acid, the rate of hydrogen generation owing to radiolysis of water, and cooling coil heat transfer. These are all functions of nitric acid concentration and air-lift circulator operation. 

P-A4 = 7.7 (47). The rates of hydrolysis of the peroxodiphosphate ion are dependent on both pH and temperature, eg, as the hydrogen ion concentration iacreases, the rate iacreases (48). Peroxodiphosphoric acid hydroly2es to peroxomonophosphoric acid according to the foUowiag equation ... 

When equal amounts of solutions of poly(ethylene oxide) and poly(acryhc acid) ate mixed, a precipitate, which appears to be an association product of the two polymers, forms immediately. This association reaction is influenced by hydrogen-ion concentration. Below ca pH 4, the complex precipitates from solution. Above ca pH 12, precipitation also occurs, but probably only poly(ethylene oxide) precipitates. If solution viscosity is used as an indication of the degree of association, it appears that association becomes mote pronounced as the pH is reduced toward a lower limit of about four. The highest yield of insoluble complex usually occurs at an equimolar ratio of ether and carboxyl groups. Studies of the poly(ethylene oxide)—poly(methacryhc acid) complexes indicate a stoichiometric ratio of three monomeric units of ethylene oxide for each methacrylic acid unit. 

Titanium corrodes very rapidly in acid fluoride environments. It is attacked in boiling HCl or H2SO4 at acid concentrations of >1% or in ca 10 wt % acid concentration at room temperature. Titanium is also attacked by hot caustic solutions, phosphoric acid solutions (concentrations >25 wt%), boiling AlCl (concentrations >10 wt %), dry chlorine gas, anhydrous ammonia above 150°C, and dry hydrogen—dihydrogen sulfide above 150°C. 

The mercurous sulfate [7783-36-OJ, Hg2S04, mercury reference electrode, (Pt)H2 H2S04(y ) Hg2S04(Hg), is used to accurately measure the half-ceU potentials of the lead—acid battery. The standard potential of the mercury reference electrode is 0.6125 V (14). The potentials of the lead dioxide, lead sulfate, and mercurous sulfate, mercury electrodes versus a hydrogen electrode have been measured (24,25). These data may be used to calculate accurate half-ceU potentials for the lead dioxide, lead sulfate positive electrode from temperatures of 0 to 55°C and acid concentrations of from 0.1 to Sm. 

The evolution of hydrogen from the acid molecule can also occur in slightly dissociated weak acids such as HjCOj and HjS. In the case of only slightly dissociated weak acids, such as HjCOj and HjS, production of hydrogen can also occur from the acid molecules. In this case, the acid concentration rather than the pH value is a measure of the aggressiveness of the corrosion. In the same way, hydrogen can be evolved from HjO ... 

Fig. 10-11. The pH scale is a measure of hydrogen ion concentration. The pH of common substances is shown with various values along the scale. The Adirondack Lakes are located in the state of New York and are considered to be receptors of acidic deposition. Source U.S. Environmental Protection Agency, Acid Rain—Research Summary," EPA-600/8-79-028, Cincinnati, 1979.

If the hydrogen peroxide is slightly below 30%, enough should be used to give the amount called for. The acid concentration should be mainlained by increasing the sulfuric acid proportionately. 

The role that acid and base catalysts play can be quantitatively studied by kinetic techniques. It is possible to recognize several distinct types of catalysis by acids and bases. The term specie acid catalysis is used when the reaction rate is dependent on the equilibrium for protonation of the reactant. This type of catalysis is independent of the concentration and specific structure of the various proton donors present in solution. Specific acid catalysis is governed by the hydrogen-ion concentration (pH) of the solution. For example, for a series of reactions in an aqueous buffer system, flie rate of flie reaction would be a fimetion of the pH, but not of the concentration or identity of the acidic and basic components of the buffer. The kinetic expression for any such reaction will include a term for hydrogen-ion concentration, [H+]. The term general acid catalysis is used when the nature and concentration of proton donors present in solution affect the reaction rate. The kinetic expression for such a reaction will include a term for each of the potential proton donors that acts as a catalyst. The terms specific base catalysis and general base catalysis apply in the same way to base-catalyzed reactions. 

Many organic reactions involve acid concentrations considerably higher than can be accurately measured on the pH scale, which applies to relatively dilute aqueous solutions. It is not difficult to prepare solutions in which the formal proton concentration is 10 M or more, but these formal concentrations are not a suitable measure of the activity of protons in such solutions. For this reason, it has been necessaiy to develop acidity functions to measure the proton-donating strength of concentrated acidic solutions. The activity of the hydrogen ion (solvated proton) can be related to the extent of protonation of a series of bases by the equilibrium expression for the protonation reaction. 

Not unexpectedly, this procedure reveals some dependence on the particular type of base used, so no universal Hq scale can be established. Nevertheless, this technique provides a very useful measure of the relative hydrogen-ion activity of concentrated acid solutions which can be used in the study of reactions that proceed only at high acid concentration. Table 4.8 gives Hq values for some water-sulfuric acid mixtures. 

Hydrogen peroxide solutions (27.5-91% by weight) Nitric acid (concentrations >70%)... 

Mathematically, pH is the logarithm (base 10) of the reciprocal of the hydrogen ion concentration. The pH may range from 0 to 14, where 0 is most acidic, 14 most basic, and 7 is neutral. Natural waters usually have a pH between 6.5 and 8.5. 

A decrease in reaction order with respect to hydrogen ion concentration witli increasing acidity has frequently been observed for reactions involving weak acids. 

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