Calculating pH in pig manure taking into account ionic strength

2008 ◽  
Vol 57 (11) ◽  
pp. 1785-1790 ◽  
Author(s):  
A. M. Nielsen ◽  
H. Spanjers ◽  
E. I. P. Volcke

Models such as the Anaerobic Digestion Model No. 1 (ADM1) assume that pH can be calculated directly from the concentration of hydrogen ions. However because pH is, by definition, the negative logarithm of the hydrogen ion activity, and thus pH measurements represent hydrogen ion activities, this approach may lead to a bias between measured and predicted pH values. Implementing ionic strength effects into the charge balance equation and the calculation of pH is a theoretical improvement to this. In this study a model, implementing a procedure for calculating pH, was developed to analyse the effect of ionic strength on pH in a pig manure. By adding KCl to samples of pig manure, experimental results could be analysed with help from the model. A modified form of the Davies equation was found to give the most accurate prediction of pH in the pig manure studied in this paper with changing ionic strength.

1927 ◽  
Vol 8 (6) ◽  
pp. 543-599 ◽  
Author(s):  
S. P. L. Sørensen ◽  
K. Linderstrøm-Lang ◽  
Ellen Lund

Introduction. A description is given of the principle followed in the experimental determination of the ionisation of egg albumin, its capacity to combine with acids and bases. Egg albumin is regarded as an ampholyte, and in accordance with J. N. Brønsted's definition of acids and bases, ampholytes are considered as substances capable of both taking up and giving off hydrogen ions. The theoretical treatment of the capacity of ampholytes to combine with acids (and bases) has been carried out on this basis. Section A. Several experimental series are noted, comprising the determination of the activity coefficient of the hydrogen ion (fH) in ammonium chloride solutions of different concentration. Section B. The general method of experimental determination of the ionisation (capacity to combine with adds and bases) of egg albumin in ammonium chloride and potassium chloride solutions is briefly described, and the results of the experiments are compared. Section C. 1). In a brief theoretical survey we have suggested that distinction should be made between isoelectric and isoionic reaction of an ampholyte, the former defined as the hydrogen ion activity (value of paH) at which the mean valency of the ampholyte is 0, the latter as the hydrogen ion activity at which the quantity of acid or base combined with the ampholyte is 0; or, as we prefer to express it, the hydrogen ion activity at which the specific hydrogen ionisation of the ampholyte is 0. If the ampholyte does not combine with other ions than the hydrogen ion, then isoelectric and isoionic reaction coincide. Isoionic reaction is determined by acid-combining experiments. The principle of this determination is briefly described. A theoretical investigation of the alteration with salt concentration of both isoelectric (isoionic) reaction and the shape and direction of the ionisation curves is made, with regard to ampholytes capable only of combining with hydrogen ions, on the basis of the Debye-Hückel formulæ and Linderstrøm-Lang's theory for the ionisation of polyvalent ampholytes of simple type. It is shown that the salt effect, in accordance with the theory, and in qualitative agreement with the experiments, consists in a turning of the ionisation curves, indicating the relation between the quantity of combined acid (specific hydrogen ionisation) and paH, and the turning of the curves, which leaves the isoelectric reaction unaltered, tends in such a direction that the quantity of combined acid at constant ampholyte concentration and constant pan increases with increasing salt concentration. The possibility of chemical combining of other ions than the hydrogen ion is discussed. 2). Following on 1), a brief survey of the experimental results is given. 3). The isoionic reaction is found from the experimental material and proved to be independent of the ammonium chloride concentration. As the mean of all determinations we have paH0 = 4.898 (isoionic reaction). The difference between this value and that formerly found for ammonium sulphate solutions (4.844) is discussed. 4). Finally, on the basis of the theory in Section 1), some simple calculations of the ionisation curves for egg albumin are made, and it appears that the theory can reproduce the experimental results in a rough quantitative way when we assume that the egg albumin has a radius of 2.21·10–7 cm. (answering to a molecular weight of 35,000 in aqueous solution), and contains 30 acid and base groups.


1984 ◽  
Vol 41 (5) ◽  
pp. 811-815 ◽  
Author(s):  
Jay J. Messer ◽  
Jimmy Ho ◽  
William J. Grenney

Previously published tabulations of percent ammonia ionization inherently define pH in terms of concentration (molality) rather than the measured entity, hydrogen ion activity. In hard waters this may result in overestimation of the un-ionized NH3 concentration by 10–20%. The thermodynamic basis for current empirical methods for temperature correction is examined, and a tabulation of NH3 ionization fraction as a function of pH, temperature, and dissolved solids, together with a corresponding predictive equation, is presented.


1932 ◽  
Vol 15 (5) ◽  
pp. 575-603 ◽  
Author(s):  
Harold A. Abramson

1. By combining the theories of Smoluchowski, Debye and Hückel, and Henry it is possible to state explicitly (making necessary assumptions) under what conditions the following simple rule should be valid for proteins: In solutions of the same ionic strength, the electric mobilities of the same protein at different hydrogen ion activities should be proportional to the number of hydrogen (hydroxyl) ions bound. 2. Data of Tiselius and of the writer confirm this rule for (a) egg albumin, (b) serum albumin, (c) deaminized gelatin and gelatin, and (d) casein. 3. On the basis of the confirmed theory the titration curves of certain proteins are predicted from their mobilities. 4. It is shown that when certain proteins are adsorbed by quartz the apparent dissociation constant of the adsorbed protein is practically unchanged. The mass law must also be valid at the phase boundary. 5. The facts of paragraphs (1) to (4) are discussed in connection with the mechanism of (a) protein adsorption, (b) enzyme activity, (c) immune reactions, (d) the calculation of the electric charge of cells, and (e) criteria of surface similarity.


1995 ◽  
Vol 30 (2) ◽  
pp. 231-242 ◽  
Author(s):  
Göran Westerström

Abstract A 200-m2 lysimeter, representing an urban paved plot, was installed in Lulea, Sweden, instrumented and monitored during the 1986 snowmelt season. Hourly and daily flow-proportional composite samples of snowmelt were collected and analyzed for pH, Cl−, NO3− and SO42− ions. The fractionation of these parameters in snowmelt was observed, indicating low pH values and high concentrations of the ions studied in the early phases of snowmelt relative to the parent snow cover. The corresponding concentration factors ranged from 5 to 8. Fluxes of hydrogen ions in snowmelt showed high values during the early phases of snowmelt, commonly described as an early (first) pollutant flush. For this type of pollutant transport response, the pollution load could be effectively controlled by storing and/or treating the initial heavily polluted part of total snowmelt and allowing the rest to bypass the control facility. By storing and/or treating the first quarter of the total meltwater volume, almost two thirds of the total hydrogen ion load could be controlled.


1930 ◽  
Vol 14 (2) ◽  
pp. 255-275 ◽  
Author(s):  
Philip H. Mitchell ◽  
Jesse P. Greenstein

1. The apparent acid and basic dissociation constants were determined potentiometrically by the methods of hydrolysis and of titration for the following ampholytes: Glycocoll, glycylglycocoll, alanylglycocoll, valylglycocoll, leucylglycocoll, methylleucylglycocoll, phenylalanylglycocoll and glycylglycylglycocoll. The constants were also determined in the presence of KCl and of K2SO4 at equal ionic strength. 2. In general, the relative order of magnitude of the constants decreased as the number of carbon atoms between amino and carboxyl groups increased. An explanation of this is offered on the basis of theories of electronic structure. 3. The application of the modern concepts of solutions to the case of the ampholytic ions is discussed. The inadequacy of the present theories is pointed out. 4. The constants were found, in general, to be functions of the hydrogen ion activity and the ionic strength of the solutions. Apparent contradictions to the Debye-Hückel theory are pointed out and partially explained on the basis of specific ion effects.


1997 ◽  
Vol 62 (11) ◽  
pp. 1730-1736 ◽  
Author(s):  
Petr Munk ◽  
Zdeněk Tuzar ◽  
Karel Procházka

When two electrolyte solutions are separated and only some of the ions can cross the boundary, the concentrations of these ions are different on both sides of the boundary. This is the well-known Donnan effect. When weak electrolytes are involved, the imbalance includes also hydrogen ions: there is a difference of pH across the boundary and the dissociation of nondiffusible weak electrolytes is suppressed. The effect is very pronounced when the concentration of the weak electrolyte is high and ionic strength is low. The significance of this phenomenon is discussed for polyelectrolyte solutions, and particularly for block copolymer micelles with weak polyelectrolyte shells. The effect is quite dramatic in the latter case.


2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Karol Postawa ◽  
Jerzy Szczygieł ◽  
Marek Kułażyński

Abstract Background Increasing the efficiency of the biogas production process is possible by modifying the technological installations of the biogas plant. In this study, specific solutions based on a mathematical model that lead to favorable results were proposed. Three configurations were considered: classical anaerobic digestion (AD) and its two modifications, two-phase AD (TPAD) and autogenerative high-pressure digestion (AHPD). The model has been validated based on measurements from a biogas plant located in Poland. Afterward, the TPAD and AHPD concepts were numerically tested for the same volume and feeding conditions. Results The TPAD system increased the overall biogas production from 9.06 to 9.59%, depending on the feedstock composition, while the content of methane was slightly lower in the whole production chain. On the other hand, the AHPD provided the best purity of the produced fuel, in which a methane content value of 82.13% was reached. At the same time, the overpressure leads to a decrease of around 7.5% in the volumetric production efficiency. The study indicated that the dilution of maize silage with pig manure, instead of water, can have significant benefits in the selected configurations. The content of pig slurry strengthens the impact of the selected process modifications—in the first case, by increasing the production efficiency, and in the second, by improving the methane content in the biogas. Conclusions The proposed mathematical model of the AD process proved to be a valuable tool for the description and design of biogas plant. The analysis shows that the overall impact of the presented process modifications is mutually opposite. The feedstock composition has a moderate and unsteady impact on the production profile, in the tested modifications. The dilution with pig manure, instead of water, leads to a slightly better efficiency in the classical configuration. For the TPAD process, the trend is very similar, but the AHPD biogas plant indicates a reverse tendency. Overall, the recommendation from this article is to use the AHPD concept if the composition of the biogas is the most important. In the case in which the performance is the most important factor, it is favorable to use the TPAD configuration.


Soil Research ◽  
1981 ◽  
Vol 19 (1) ◽  
pp. 93 ◽  
Author(s):  
GP Gillman

The cation exchange capacity of six surface soils from north Queensland and Hawaii has been measured over a range of pH values (4-6) and ionic strength values (0.003-0.05). The results show that for variable charge soils, modest changes in electrolyte ionic strength are as important in their effect on caton exchange capacity as are changes in pH values.


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