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Not all solutions of weak acids or bases function as effective buffers
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Reference literature notes that specific preparation guidelines, such as choosing appropriate pKa ranges and maintaining sufficient conjugate ratios, determine whether weak acid or base solutions function as effective buffers.

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1993 · cited by 5
AbstractA general theory for buffers consisting of one weak acid and one weak base is developed, particular interest being devoted to the special case of doubly weak salts. The pH course as it varies with the acid/base concentration ratio is presented in equations and graphs. The influence of ΔpK′ = pK′b−pK′a, which can be negative as well as positive, is discussed and visualized in graphs. The buffer capacity is deduced as a function of pH. The buffer range is, at a maximum, 2.67 times that of a monovalent weak protolyte for ΔpK′ = 2.7 pH units. The buffer capacity curve has two maxima for ΔpK′ values bigger than 0.77. For negative ΔpK′ values the buffer capacity curve has only one maximum, and the buffer range is not better than that of a monovalent protolyte. A general equation for the ionic concentrations is deduced, and as a corollary the degree of hydrolysis of the doubly weak salt is obtained as a function of ΔpK′. For solutions of this salt, the relation between concentration and pH is elucidated by equations and graphs.
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Greater concentrations will withstand greater additions of base or acid while still resisting a significant pH change. If we were to add so much acid so that it reacted with all of the base in a buffer system, the buffering capacity of the system would be exceeded, and further additions of acid would result in large changes in pH. A guideline for preparing a buffer system is to choose an acid with a pKa within one pH unit of the desired buffer. This ensures that the ratio of base to acid will range between 1 to 10 and 10 to 1, and thus sufficient quantities of both acid and base will be present in the buffering system. pH Titration A pH titration is performed by adding small amounts of a titrant to a solution and simultaneously monitoring the solution pH. A typical titration would be to add small amounts of sodium hydroxide solution to a weak acid solution. In this case, the pH during the titration is related to the pKa of the weak acid. During the titration, acid is being converted to its conjugate base, and a buffer solution is formed. You should try to answer the questions without referring to your textbook. If you get stuck, try asking another group for help. An important property of blood and other physiological components is that they resist change in pH. A buffer system occurs when a weak acid and its conjugate base are present in the same solution. For instance, blood has a pH of about 7.4, and complex chemical systems work to maintain that pH. The most important component of those systems is the carbonic acid buffer system. Not by coincidence, this happens to be the same weak acid found in soft drinks. Buffer systems are an important application of acid–base equilibria. The study of acid–base equilibria is very useful because many other chemical systems can be understood through the same mathematical approach. The most common experimental method used to study acid–base systems is titration analysis, through which we can determine the pK a of a weak acid and the pK b of its conjugate base, the two essential components of a buffer. The Buffer Equation (Henderson-Hasselbach Approximation) Let’s consider a weak acid equilibrium system and its corresponding equilibrium constant: \[HA(aq) \rightleftharpoons H^+(aq) + A^–(aq) \nonumber \] with \[K_a = \dfrac{[H^+] [A^–]}{[HA]} \label{2} \] where \(HA\) represents a weak monoprotic acid, and \(A^–\) is its conjugate base. However, we often find it useful and accurate to make the approximation that the weak acid is only slightly dissociated. Thus the equilibrium concentration of HA is approximately equal to the initial concentration, or \[[HA]_{eq} \approx [HA]_o \nonumber \] A similar assumption is also valid for weak bases: \[[A^–]_{eq} \approx [A^–]_o \nonumber \] The Effectiveness of a Buffer Consider a 100.0 mL solution containing 0.010 mol acetic acid, \(HC_2H_3O_2\), and 0.010 mol sodium acetate, \(NaC_2H_3O_2\). We have \[[A^–][HA] = 1 \nonumber \] and \[\log 1 = 0 \nonumber \] therefore, \(pH = pK_a\). Looking up \(pK_a\) for acetic acid, we find \(pH = pK_a = 4.75\). Now let’s consider what will happen if we add 0.005 mol of HCl to this solution. The strong acid will react with the acetate ion. ICE Table \(H^+(aq)\) \(C_2H_3O^{2–}(aq)\) \(\rightleftharpoons\) \(HC_2H_3O_2(aq)\) I nitial 0.005 0.010 0.010 C hange – 0.005 – 0.005 + 0.005 E quilibrium 0 0.005 0.015 The buffer equation can now be applied to determine the new solution pH: \[pH = pKa + \log_{10} \dfrac{[A^–]}{[HA]} = 4.75 + \log_{10} \left( \dfrac{0.005 \,mol/0.1000 \,L}{0.015 \,mol/0.1000\, L} \right) = 4.27 \nonumber \] The pH of the solution changes from 4.75 to 4.27 upon addition of the acid. The Ineffectiveness of a Non-buffer Let’s compare this to what will happen if we add the same amount of \(HCl\) to a nonbuffered solution that begins at pH = 4.75. A \(1.8 \times 10^{–5} M\) \(HCl\) solution has a pH of 4.75 (full dissociated). The number of moles of \(H^+(aq)\) in this solution is \[(0.1000 L )(1.8 \times 10^{–5} mol L ) = 1.8 A consideration that must be made when preparing a buffer is to have sufficient quantities of both the weak acid and its conjugate base to completely react with any base or acid that may be added to the system. The buffer capacity of a system is defined in terms of the concentrations of the acid–base conjugate pair. Greater concentrations will withstand greater additions of base or acid while still resisting a significant pH change. If we were to add so much acid so that it reacted with all of the base in a buffer system, the buffering capacity of the system would be exceeded, and further additions of acid would result in large changes in pH. A guideline for preparing a buffer system is to choose an acid with a pK a within one pH unit of the desired buffer. This ensures that the ratio of base to acid will range between 1 to 10 and 10 to 1, and thus sufficient quantities of both acid and base will be present in the buffering system. pH Titration A pH titration is performed by adding small amounts of a titrant to a solution and simultaneously monitoring the solution pH. A typical titration would be to add small amounts of sodium hydroxide solution to a weak acid solution. In this case, the pH during the titration is related to the pKa of the weak acid. During the titration, acid is being converted to its conjugate base, and a buffer solution is formed. Eventually, the quantity of base added is such that all of the acid has been converted to its conjugate base, and the equivalence point of the titration has been reached. The solution is no longer a buffer at the equivalence point. Outside Links Barnum, Dennis W. "Predicting Acid-Base Titration Curves without Calculations." J. Chem. Educ. 1999 76 938. de Levie, Robert. "A General Simulator for Acid-Base Titrations." J. Chem. Educ. 1999 76 987.
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  1. LibreTexts: Buffers and Titration Curves (Worksheet)referenceno side taken
  2. On the use of dimensionless parameters in acid‐base theory. V. Buffers composed of binary mixtures of monovalent weak acids and basespeer-reviewedsame source L2no side taken
  3. On the use of dimensionless parameters in acid‐base theory. V. Buffers composed of binary mixtures of monovalent weak acids and basespeer-reviewedsame source L2no side taken
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