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Difference between revisions of "Advancement"

From Bioblast
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|info=[[Gnaiger_1993_Pure Appl Chem |Gnaiger (1993) Pure Appl Chem]], [[Gnaiger 2020 BEC MitoPathways]]
|info=[[Gnaiger_1993_Pure Appl Chem |Gnaiger (1993) Pure Appl Chem]], [[Gnaiger 2020 BEC MitoPathways]]
}}
}}
Ā  Communicated by [[Gnaiger E]] (last update 2018-11-02)
Ā  Communicated by [[Gnaiger E]] (2018-11-02) last update 2021-01-27
[[File:Advancement Table 1 Gnaiger 1993 Pure Appl Chem.png|400px|link=Gnaiger 1993 Pure Appl Chem |thumb|d<sub>el</sub>''Q''<sub>''i''</sub> (d<sub>th</sub>''Q''<sub>''i''</sub>) are the changes in electric charge (heat) at the compartments of high or low electric potential (temperature) within the discontinuous system (from ref. [2]).]]
Ā 
== Synonyms ==
::::* advancement
::::* extent (of reaction)
::::* displacement (of a moving particle)


[[File:Advancement Table 1 Gnaiger 1993 Pure Appl Chem.png|400px|link=Gnaiger 1993 Pure Appl Chem |thumb|d<sub>el</sub>''Q''<sub>''i''</sub> (d<sub>th</sub>''Q''<sub>''i''</sub>) are the changes in electric charge (heat) at the compartments of high or low electric potential (temperature) within the discontinuous system (from ref. [2]).]]


== Advancement per volume ==
== Advancement per volume ==
:::: The advancement of a transformation in a closed homogenous system (chemical reaction) or discontinuous system (diffusion) causes a change of [[concentration]] of substances ''i''. Ā 
:::: The advancement of a transformation in a closed homogenous system (chemical reaction) or discontinuous system (diffusion) causes a change of [[concentration]] of substances ''i''. Ā 
:::: The advancement causes a ''change'' of concentration due to a transformation, Ī”<sub>tr</sub>''c'', in contrast to a difference of concentrations calculated between difference states, Ī”<sub>tr</sub>''c''. Ā 
:::: The advancement causes a ''change'' of concentration due to a transformation, Ī”<sub>tr</sub>''c'', in contrast to a difference of concentrations calculated between difference states, Ī”<sub>tr</sub>''c''. Ā 
::::Ā» [[Advancement per volume]], d<sub>tr</sub>''Y'' = d<sub>tr</sub>''Ī¾''āˆ™V<sup>-1</sup>
::::Ā» [[Advancement per volume]], d<sub>tr</sub>''Y'' = d<sub>tr</sub>''Ī¾''āˆ™''V''<sup>-1</sup>




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:::# Gnaiger E (1993) Nonequilibrium thermodynamics of energy transformations. Pure Appl Chem 65:1983-2002. - [[Gnaiger 1993 Pure Appl Chem |Ā»Bioblast linkĀ«]]
:::# Gnaiger E (1993) Nonequilibrium thermodynamics of energy transformations. Pure Appl Chem 65:1983-2002. - [[Gnaiger 1993 Pure Appl Chem |Ā»Bioblast linkĀ«]]
:::# Prigogine I (1967) Introduction to thermodynamics of irreversible processes. Interscience New York, 3rd ed:147 pp. - [[Prigogine 1967 Interscience |Ā»Bioblast linkĀ«]] Ā 
:::# Prigogine I (1967) Introduction to thermodynamics of irreversible processes. Interscience New York, 3rd ed:147 pp. - [[Prigogine 1967 Interscience |Ā»Bioblast linkĀ«]] Ā 
:::# Grosholz Emily R (2007) Representation and productive ambiguity in mathematics and the sciences. Oxford Univ Press 312 pp. - [[Prigogine 1967 Interscience |Ā»Bioblast linkĀ«]] ā€” ".. distance that is re-conceptualized to mean displacement, since we are instructed to suppose that a moving particle is traversing it."


{{Keywords: Force and membrane potential}}
{{Keywords: Force and membrane potential}}

Revision as of 14:37, 27 January 2021


high-resolution terminology - matching measurements at high-resolution


Advancement

Description

In an isomorphic analysis, any form of flow is the advancement of a process per unit of time, expressed in a specific motive unit [MUāˆ™s-1], e.g., ampere for electric flow or current, Iel = delĪ¾/dt [Aā‰”Cāˆ™s-1], watt for thermal or heat flow, Ith = dthĪ¾/dt [Wā‰”Jāˆ™s-1], and for chemical flow of reaction, Ir = drĪ¾/dt, the unit is [molāˆ™s-1] (extent of reaction per time). The corresponding motive forces are the partial exergy (Gibbs energy) changes per advancement [Jāˆ™MU-1], expressed in volt for electric force, Ī”elF = āˆ‚G/āˆ‚elĪ¾ [Vā‰”Jāˆ™C-1], dimensionless for thermal force, Ī”thF = āˆ‚G/āˆ‚thĪ¾ [Jāˆ™J-1], and for chemical force, Ī”rF = āˆ‚G/āˆ‚rĪ¾, the unit is [Jāˆ™mol-1], which deserves a specific acronym [Jol] comparable to volt [V]. For chemical processes of reaction (spontaneous from high-potential substrates to low-potential products) and compartmental diffusion (spontaneous from a high-potential compartment to a low-potential compartment), the advancement is the amount of motive substance that has undergone a compartmental transformation [mol]. The concept was originally introduced by De Donder [1]. Central to the concept of advancement is the stoichiometric number, Ī½i, associated with each motive component i (transformant [2]).

In a chemical reaction r the motive entity is the stoichiometric amount of reactant, drni, with stoichiometric number Ī½i. The advancement of the chemical reaction, drĪ¾ [mol], is defined as,

drĪ¾ = drniĀ·Ī½i-1

The flow of the chemical reaction, Ir [molĀ·s-1], is advancement per time,

Ir = drĪ¾Ā·dt-1

This concept of advancement is extended to compartmental diffusion and the advancement of charged particles [3], and to any discontinuous transformation in compartmental systems [2],

Advancement.png

Abbreviation: dtrĪ¾ [MU]

Reference: Gnaiger (1993) Pure Appl Chem, Gnaiger 2020 BEC MitoPathways

Communicated by Gnaiger E (2018-11-02) last update 2021-01-27
delQi (dthQi) are the changes in electric charge (heat) at the compartments of high or low electric potential (temperature) within the discontinuous system (from ref. [2]).

Synonyms

  • advancement
  • extent (of reaction)
  • displacement (of a moving particle)


Advancement per volume

The advancement of a transformation in a closed homogenous system (chemical reaction) or discontinuous system (diffusion) causes a change of concentration of substances i.
The advancement causes a change of concentration due to a transformation, Ī”trc, in contrast to a difference of concentrations calculated between difference states, Ī”trc.
Ā» Advancement per volume, dtrY = dtrĪ¾āˆ™V-1


References

  1. De Donder T, Van Rysselberghe P (1936) Thermodynamic theory of affinity: a book of principles. Oxford, England: Oxford University Press:144 pp.
  2. Gnaiger E (1993) Nonequilibrium thermodynamics of energy transformations. Pure Appl Chem 65:1983-2002. - Ā»Bioblast linkĀ«
  3. Prigogine I (1967) Introduction to thermodynamics of irreversible processes. Interscience New York, 3rd ed:147 pp. - Ā»Bioblast linkĀ«
  4. Grosholz Emily R (2007) Representation and productive ambiguity in mathematics and the sciences. Oxford Univ Press 312 pp. - Ā»Bioblast linkĀ« ā€” ".. distance that is re-conceptualized to mean displacement, since we are instructed to suppose that a moving particle is traversing it."


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Bioblast links: Force and membrane potential - >>>>>>> - Click on [Expand] or [Collapse] - >>>>>>>
Fundamental relationships
Ā» Force
Ā» Affinity
Ā» Flux
Ā» Advancement
Ā» Advancement per volume
Ā» Stoichiometric number
mt-Membrane potential and protonmotive force
Ā» Protonmotive force
Ā» Mitochondrial membrane potential
Ā» Chemical potential
Ā» Faraday constant
Ā» Format
Ā» Uncoupler
O2k-Potentiometry
Ā» O2k-Catalogue: O2k-TPP+ ISE-Module
Ā» O2k-Manual: MiPNet15.03 O2k-MultiSensor-ISE
Ā» TPP - O2k-Procedures: Tetraphenylphosphonium
Ā» Specifications: MiPNet15.08 TPP electrode
Ā» Poster
Ā» Unspecific binding of TPP+
Ā» TPP+ inhibitory effect
O2k-Fluorometry
Ā» O2k-Catalogue: O2k-FluoRespirometer
Ā» O2k-Manual: MiPNet22.11 O2k-FluoRespirometer manual
Ā» Safranin - O2k-Procedures: MiPNet20.13 Safranin mt-membranepotential / Safranin
Ā» TMRM - O2k-Procedures: TMRM
O2k-Publications
Ā» O2k-Publications: mt-Membrane potential
Ā» O2k-Publications: Coupling efficiency;uncoupling



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MitoPedia concepts: MiP concept, Ergodynamics