Which value for the first dissociation constant of carbonic acid should be used in biological work?

1991 ◽  
Vol 260 (5) ◽  
pp. C1113-C1116 ◽  
Author(s):  
R. W. Putnam ◽  
A. Roos

The apparent first dissociation constant of carbonic acid has been defined in different ways in the literature. Harned and co-workers (8-10) have defined it in terms of molalities of the participating species, including H ions: Ks = mHmHCO3/mCO2. In contrast, Hastings and Sendroy have defined an apparent constant in which acidity is expressed as H ion activity: K'1 = aHmHCO3/mCO2. These constants differ by a factor gamma H, the activity coefficient of H ions at the prevailing ionic strength. Therefore, pK'1 is greater than pKs by an amount equal to -log gamma H, which, at mu = 0.16 M, is approximately 0.1. It is important that the correct value for the apparent dissociation constant or its logarithmic form be entered in the mass action expression or in the Henderson-Hasselbalch equation in order to prevent significant errors in the computation by means of these equations of quantities that cannot be directly measured. Specifically, for the derivation of bicarbonate concentration from PCO2 and pH (-log aH), pK'1 is to be used and not an uncorrected pKs.

1989 ◽  
Vol 257 (1) ◽  
pp. C29-C35 ◽  
Author(s):  
J. P. Manfredi ◽  
R. Marquetant ◽  
A. D. Magid ◽  
E. W. Holmes

The muscle isozyme of adenylosuccinate synthetase (AdSS), an enzyme of the purine nucleotide cycle, has previously been shown to bind to purified F-actin in buffers of low ionic strength and pH (Ogawa et al. Eur. J. Biochem. 85: 331-338, 1978). We have extended these observations by measuring the association of both crude and purified AdSS with the contractile proteins of muscle in buffers of physiological ionic strength and pH. Under these conditions, the enzyme binds to F-actin, actin-tropomyosin complexes, reconstructed thin filaments, and myofibrils but not to myosin. The apparent dissociation constant of 1.2 microM and binding maximum of 2.6 nmol enzyme/mg myofibrils indicate that binding of AdSS to myofibrils can be physiologically significant. The results suggest that AdSS in muscle may be associated with the thin filament of myofibrils.


2018 ◽  
Vol 61 (2) ◽  
pp. 559-570
Author(s):  
Dyan L. Pratt ◽  
Terrance A. Fonstad

Abstract. In the event of a mass livestock mortality situation, disposal routes such as burial are commonly chosen. The impact of burial on the environment could be substantial, but the composition of the leachate arising from a burial site has not been well documented. This study was performed to determine the chemical composition of leachate arising from animal mortalities in a burial setting. Three species of livestock were used: bovine, swine, and poultry. Leachate collected from lined burial pits over two years of decomposition was analyzed for major and minor ions. Analysis indicated that livestock mortality leachate contains, on average, concentrations of 46,000 mg L-1 of alkalinity (as bicarbonate), 12,600 mg L-1 of ammonium-N, 2600 mg L-1 of chloride, 3600 mg L-1 of sulfate, 2300 mg L-1 of potassium, 1800 mg L-1 of sodium, and 1500 mg L-1 of phosphorus, along with lesser amounts of iron, calcium, and magnesium. Select samples had maximum concentrations of ammonium-N and bicarbonate up to 50% higher than these average values. In comparison to earthen swine manure storages and landfills, the ionic strength of the leachate was 2 to 4 times higher, and therefore its impact on water resources could be greater. Following the study of the chemical composition of livestock mortality leachate, the potential impacts of this leachate on the soil/water systems below a burial site were investigated. The ionic strength of the leachate presents its own set of challenges. Basic modeling of ion activity using the five most common activity coefficient equations (Debye-Hückel, extended Debye-Hückel, Truesdell-Jones, Davies, and Pitzer) were considered to assess the sensitivity of these methods for calculated ion activity as impacted by the ionic strength of the leachate. This was completed to further enhance the modeling and speciation efforts. Based on the results and the applicability of the Truesdell-Jones equation, PHREEQC was used to assess the chemical speciation of the leachate. The speciation of this leachate provides evidence of phosphate and sulfate compounds available for potential unattenuated transport. Understanding the geochemical implications of livestock mortality burial will give scientists and regulators more information for performing future risk analyses when considering mortality burial as a management option, either routinely or during a mass mortality event. Keywords: Ion activity coefficient, Ionic strength, Leachate chemical composition, Livestock burial leachate, Speciation.


1950 ◽  
Vol 27 (2) ◽  
pp. 158-174 ◽  
Author(s):  
L. LEVENBOOK

1. The pH of the blood of the third instar Gastrophilus larva is 6.64 at 38° C. with a pH-temperature coefficient of -0.007 Per 1° C. rise in temperature. 2. The total CO2 content of the blood varies from 40.6 to 131.4 vol. % with an average of 72.4 vol. %. The CO2 content of the tissues minus the cuticle is very close to, and follows the variations in, the CO2 content of the blood. 3. The CO2 tension in the blood is from 300 to 500 mm. Hg. From 30 to 50% of the CO2 is in solution, the rest in the form of bicarbonate. Carbamate formation does not occur in the blood. 4. The ‘apparent’ dissociation constant for carbonic acid, (pK'1), has a value of 6.08 (S.D. ±0.06) at 38° C. and 6.19 (s.d. ±0.13) at 16° C. 5. CO2 dissociation curves have been drawn for 38 and 16° C. The slope of the curves indicates that the whole of the CO2 is given off at zero CO2 tension, and that the blood is adapted for functioning at high CO2 tensions.


1955 ◽  
Vol 6 (1) ◽  
pp. 115 ◽  
Author(s):  
AW Turner ◽  
VE Hodgetts

Experiments are described which emphasize the importance of avoiding loss of carbon dioxide when estimating the pH or bicarbonate concentration of ruminal fluid. The high pCO2 of ruminal fluid is stressed; this may be 10 times or more as great as that of arterial blood. The relationship between pCO2, pH, and [HCO3-] was examined in terms of the Henderson-Hasselbalch equation over a wide range of pCO2. From this, the pK1' of the carbonic acid system in four ruminal fluids was determined as 6.21-6.28, mean 6.25. The higher pH of saliva-free samples of ruminal fluid withdrawn by suction through a tube passed down the oesophagus, as compared with that of the bulk fluid obtained through a ruminal fistula, is considered to be due to loss of carbon dioxide during collection. A better estimate of intraruminal pH is obtained, even when salivary contamination occurs, if such samples are equilibrated with a sample of the animal's ruminal gas; if this is not practicable, an arbitrary gas mixture of high pCO2, e.g. 50 per cent. carbon dioxide and nitrogen, may be used.


1994 ◽  
Vol 2 (2) ◽  
pp. 101-107 ◽  
Author(s):  
I. Mottet ◽  
R. Demeure ◽  
B. Gallez ◽  
C. Grandin ◽  
B. E. Van Beers ◽  
...  

2003 ◽  
Vol 81 (12) ◽  
pp. 1462-1470 ◽  
Author(s):  
Jaakko I Partanen ◽  
Pekka M Juusola ◽  
Pentti O Minkkinen ◽  
Virginie Verraes

Equations were determined for the calculation of the second stoichiometric (molality scale) dissociation constant, Km2, of glycine, in aqueous NaCl and KCl solutions at 298.15 K, from the thermodynamic dissociation constant, Ka2, of this acid and the ionic strength, Im, of the solution. The ionic strength of the solutions considered in this study is determined mostly by the salt alone, and the equations for Km2 were based on the single-ion activity coefficient equations of the Hückel type. New data measured by potentiometric titrations in a glass electrode cell were used in the estimation of the parameters for the Hückel equations of glycine species. By means of the calculation method suggested in this study, Km2 can be obtained almost within experimental error up to an Im of about 1.0 mol kg–1 for glycine in NaCl and KCl solutions. The Km2 values obtained by these methods were also compared with the values suggested in the literature for this quantity.Key words: ionic strength dependence, stoichiometric dissociation constant, Debye–Hückel equation, potentiometry, glycine.


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