scholarly journals Intelligent Numerical Computing Methods for Determining the Concentration of Citric Acid by Accurate Measurement and Calculation

2021 ◽  
Vol 2083 (3) ◽  
pp. 032089
Author(s):  
Yueyang Fu

Abstract According to the Bronsted-Lowry theory, an acid is a proton donor, and a base is a proton acceptor. An acid-base reaction involves the proton transfer between chemicals, where a base containing hydroxide ion (OH-) accepts a proton (H+) from an acidic solution to form water (Khan,2016). In the above equation, HCl as an acid donates one H+ ion, and NaOH as a base accepts the proton to form one water molecule (H2O). So, a proton from the acid is transferred to the anion of the base. Then, the metal cation (Na+) and the conjugate base anion (Cl-) form the salt NaCl.

2010 ◽  
Vol 8 (4) ◽  
pp. 766-782
Author(s):  
Oleksiy Grygorovych ◽  
Oleksiy Nevskii ◽  
Sofia Moskalenko ◽  
Vasyl Pivovarenko ◽  
Andrey Doroshenko

AbstractProtolytic interactions in the series of prospective fluorescent ratiometric wide-range pH indicators — structurally rigid analogs of 2,6-distyrylpyridine — (3E,5E)-3,5-dibenzylidene-8-phenyl-1,2,3,5,6,7-hexahydrodicyclopentano[b,e]pyridine — were investigated. The pyridine nitrogen atom basicity in these compounds is significantly lower in comparison with that of unsubstituted heterocycle and 2,6-distyrylpyridine. The photochemical E→Z photoisomerization and the side benzene rings substituents influence on the acid-base equilibria were studied. The complex multi-stage mechanism of the acid-base interactions of the polysubstituted compounds was elucidated. The most significant spectral effects were typical to the N,N-dialkylamino substituted compounds of the investigated series. The widest pH sensitivity interval covering nearly the full range of 0–14 units was demonstrated for compounds with both proton donor and proton acceptor substituents.


Reactions ◽  
2011 ◽  
Author(s):  
Peter Atkins

One of the most remarkable chemists of the twentieth century, Gilbert Lewis (1875–1946), who died in a rather peculiar event involving cyanide (which will figure further in this account) took the story of acids and bases that I described in Reaction 2, extended its reach, and thereby captured a further huge swathe of chemical countryside. As I remarked in that section, chemists seek patterns of behaviour, partly because it systematizes their subject but also because it gives insight into the molecular events accompanying a reaction. Lewis contributed greatly to this enlargement of chemistry’s vision, as I shall unfold in this section. I explained in Reaction 2 how Lowry and Brønsted had extended Arrhenius’s vision of acids and bases by proposing that all reactions between acids and bases involve the transfer of a proton (a hydrogen ion, H+) from the acid, the proton donor, to the base, the proton acceptor. For instance, hydrochloric acid, HCl, can provide a proton that sticks to an ammonia molecule, NH3, 1, converting it into NH4+, 2. The Lowry–Brønsted account of an acid–base reaction involves a proton as an essential part of the definition: if protons aren’t around, then Lowry and Brønsted are silent on whether a substance is an acid or a base. There are, however, many reactions that resemble acid–base reactions but in which no protons are transferred. I will give what might seem to be a rather esoteric example, but it makes the point in a simple and direct way, so please bear with me; you will soon see the relevance of this presentation to everyday life. The esoteric example I have in mind is a reaction in which a boron trifluoride molecule, BF3, 3, sticks to an ammonia molecule to form NH3BF3, 4. This reaction clearly resembles the proton transfer reaction in which H+ attaches to NH3 to form NH4+, but with BF3 playing the role of H+. Lewis brought these aspects together in a very simple idea in 1923, at about the same time as Lowry and Brønsted made their proposals. A base, he proposed, is any species that can use two of its electrons to attach to an incoming species.


2017 ◽  
Author(s):  
Herbert Chen ◽  
Jason Primus ◽  
Colin Martin

This review is a summary of the acid-base physiology that is essential to understanding acid-base pathophysiology. An acid is defined as a proton donor; a base is defined as a proton acceptor. The body fluids are composed of acids and bases, which are tightly regulated by our organ systems, specifically the respiratory system and kidneys. Derangements in the body’s acid-base homeostatic mechanisms or overloading the capacity of the body’s ability to respond can lead to acid-base disorders. These include acidosis and alkalosis, which can be further classified into respiratory, metabolic, or mixed disorders. The approach to these disorders is to stabilize the patient, focusing on respiratory and circulatory status and treating the underlying cause of the acid-base derangement. This review contains 4 highly rendered figures, 2 tables, and 26 references. Key words: acid-base disorders, acid-base homeostasis, acid-base physiology, acidemia, alkalemia, metabolic acidosis, metabolic alkalosis, mixed acid-base disorders, respiratory acidosis, respiratory alkalosis 


2017 ◽  
Author(s):  
Herbert Chen ◽  
Jason Primus ◽  
Colin Martin

This review is a summary of the acid-base physiology that is essential to understanding acid-base pathophysiology. An acid is defined as a proton donor; a base is defined as a proton acceptor. The body fluids are composed of acids and bases, which are tightly regulated by our organ systems, specifically the respiratory system and kidneys. Derangements in the body’s acid-base homeostatic mechanisms or overloading the capacity of the body’s ability to respond can lead to acid-base disorders. These include acidosis and alkalosis, which can be further classified into respiratory, metabolic, or mixed disorders. The approach to these disorders is to stabilize the patient, focusing on respiratory and circulatory status and treating the underlying cause of the acid-base derangement. This review contains 4 highly rendered figures, 2 tables, and 26 references. Key words: acid-base disorders, acid-base homeostasis, acid-base physiology, acidemia, alkalemia, metabolic acidosis, metabolic alkalosis, mixed acid-base disorders, respiratory acidosis, respiratory alkalosis   


1975 ◽  
Vol 53 (4) ◽  
pp. 604-609 ◽  
Author(s):  
J. Vaes ◽  
F. Foubert ◽  
Th. Zeegers-Huyskens

The stability constants of complexes formed between ethanol and phenols with some N,N-dimethyl-N′-phenylformamidine derivatives are determined by i.r. spectrometry. The application of the Hammett relation shows the existence, in addition to the first degree terms depending on the substitution parameters of the proton donor (∑σa) and the proton acceptor (∑σb), of a crossed term depending on the ∑σa∑σb product. The different parameters are discussed as a function of the acid–base properties of the molecules. The results suggest that the formation of the hydrogen bond takes place on the imino nitrogen atom. The stability constant of the complexes of 2:1 stoichiometry is calculated; in this complex the second molecule of phenol seems to be preferentially bonded to the oxygen atom of the first molecule rather than to the amino nitrogen atom.


Author(s):  
Oleg A. Petrov ◽  
Aleksandr S. Semeykin ◽  
Mariya V. Shilovskaya ◽  
Tatiana V. Lyubimova

The reaction of acid-base interaction of octa(4-tert-butylphenyl)tetrapyrazinophosphyrazine with pyridine, 2-methylpyridine, morhpoline, pipyridine, n-butylamine, tert-butylamine, diethylamine, triethylamine and dimethylsulfoxide in benzene was investigated. It is shown that the researched porphyrazine forms kinetically stable proton transfer complexes with pyridine, 2-methylpyridine, morpholine and dimethylsulfoxide. In benzene-base system an acid-base equilibrium between the molecular form of octa(4-tert-butylphenyl)tetrapyrazinoporphyrazine and its proton transfer complex was established. The interaction of substituted tetrapyrazinoporphyrazine with morpholine in benzene was revealed to be a kinetically controllable process which occurs with low reaction rate and high values of activation energy. Such values are not inherent to most of relatively simple liquid-phase acid-base systems. The kinetic equation of the process was found, and, based on the spectral changes accompanying the reaction, a cheme of two-stage process of proton transfer of NH-groups of octa(4-tert-butylphenyl)tetrapyrazinoporphyrazine to morpholine in benzene was proposed. A possible structure of proton transfer complex of octa(4-tert-butylphenyl)tetrapyrazinoporphyrazine with organic bases is shown. In these complexes the inner hydrogen atoms of the cycle, bonded with base molecules, lie under and above the plane of the molecule, and the proton transfer from acid to base is limited either by the H-complex or the ion-ion associates constituting an H-bonded ion pair. Depending on the proton accepting tendency of the base, the acid-base equilibrium can shift towards or away from the more or less polarized structure. It was revealed that in benzene - n-butylamine (tri-butylamine, diethylamine, triethylamine, pipyridine) system the acid-base interaction involving octa(4- tert-butylphenyl)tetrapyrazinoporphyrazine occurs incredibly fast, with rates not measurable by standard spectrophotography methods. The forming proton transfer complexes are highly labile due to concurrent proton reaction occurring, leading to the formation of dianion form of octa(4- tert-butylphenyl)tetrapyrazinoporphyrazine. This form undergoes spontaneous dissolution into low-molecular colorless products due to the lack of compensation of excess charge in the macrocycle.


2013 ◽  
Vol 288 (29) ◽  
pp. 21254-21265 ◽  
Author(s):  
Sergei P. Balashov ◽  
Lada E. Petrovskaya ◽  
Eleonora S. Imasheva ◽  
Evgeniy P. Lukashev ◽  
Andrei K. Dioumaev ◽  
...  

A lysine instead of the usual carboxyl group is in place of the internal proton donor to the retinal Schiff base in the light-driven proton pump of Exiguobacterium sibiricum (ESR). The involvement of this lysine in proton transfer is indicated by the finding that its substitution with alanine or other residues slows reprotonation of the Schiff base (decay of the M intermediate) by more than 2 orders of magnitude. In these mutants, the rate constant of the M decay linearly decreases with a decrease in proton concentration, as expected if reprotonation is limited by the uptake of a proton from the bulk. In wild type ESR, M decay is biphasic, and the rate constants are nearly pH-independent between pH 6 and 9. Proton uptake occurs after M formation but before M decay, which is especially evident in D2O and at high pH. Proton uptake is biphasic; the amplitude of the fast phase decreases with a pKa of 8.5 ± 0.3, which reflects the pKa of the donor during proton uptake. Similarly, the fraction of the faster component of M decay decreases and the slower one increases, with a pKa of 8.1 ± 0.2. The data therefore suggest that the reprotonation of the Schiff base in ESR is preceded by transient protonation of an initially unprotonated donor, which is probably the ϵ-amino group of Lys-96 or a water molecule in its vicinity, and it facilitates proton delivery from the bulk to the reaction center of the protein.


2009 ◽  
Vol 106 (44) ◽  
pp. 18539-18544 ◽  
Author(s):  
E. W. Debler ◽  
R. Muller ◽  
D. Hilvert ◽  
I. A. Wilson

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