Association Constant

14,000,000 Leading Edge Experts on the ideXlab platform

Scan Science and Technology

Contact Leading Edge Experts & Companies

Scan Science and Technology

Contact Leading Edge Experts & Companies

The Experts below are selected from a list of 47448 Experts worldwide ranked by ideXlab platform

Jiazhen Yang - One of the best experts on this subject based on the ideXlab platform.

  • thermodynamics of ion pairs in mixed solvents i the standard Association Constant of the ion pair mgso4 oin 0 03226 co nh2 2 0 96774 h2o
    The Journal of Chemical Thermodynamics, 2001
    Co-Authors: Jiazhen Yang, Rubo Zhang, Hong Liu, Jie Wang
    Abstract:

    Abstract The standard potential of the (Ag, AgCl) electrode E o , the standard second ionization Constant of sulfuric acid K 2 , and the standard Association Constant of the ion pair [MgSO 4 ] o , K in {0.03226 CO(NH 2 ) 2  +  0.96774 H 2 O } at five temperatures from 278.15 K to 318.15 K were determined from precise e.m.f. measurements of different cells without liquid junction. The dependence of p K on temperature T is expressed by the empirical equation p K  =  6.617  −  777.9 · ( K  /  T )  −  0.02001 · ( T  /  K ). The other thermodynamic functions of the Association process were also calculated and show that the driving force for the process is the entropy of Association.

  • thermodynamics of ionic Association 1 the standard Association Constant of the ion pair li b oh 4
    Thermochimica Acta, 2000
    Co-Authors: Jiazhen Yang, Bai Sun, Pengsheng Song
    Abstract:

    Abstract Values of emf for the cell without liquid junction Pt, H 2 (101.325 kPa) |Li 2 B 4 O 7 ( m 1 ), LiCl ( m 2 )|AgCl–Ag are reported at five temperatures from 278.15 to 318.15 K. The standard Association Constant of ionic pair Li + B(OH) 4 − , K a , is determined by a fitting with the cell results. The dependence of p K a on temperature T is expressed in empirical equation: p K a =−131.6 K / T −0.08996−1.856×10 −3 T / K . The other thermodynamic quantities of the Association process are calculated and show that there truly exists ion pair Li + B(OH) 4 − and the driving force for the ion Association reaction is Association entropy.

  • thermodynamic study of aqueous borates iii the standard Association Constant of the ion pair li b oh 4
    The Journal of Chemical Thermodynamics, 1997
    Co-Authors: Jiazhen Yang, Pengsheng Song, Dongbao Wang
    Abstract:

    Abstract Values of e.m.f. for the cell without liquid junction: Pt H 2 ( p = 101.325kPa)|K 2 B 4 0 7 ( m 1 ) LiCl( m 2 )|AgCl Ag are reported at seven Constant ionic strengths from 0.07 to 2.0 mol·kg −1 at five temperatures from 278.15 K to 318.15 K. The standard Association Constant K a of the ionic pair Li + B(OH) 4 − , is determined by a fit with the cell results. The dependence of p K a on temperature T is expressed by the empirical equation: p K a = −149.8(K/ T ) + 0.09024 − 2.112·10 −3 ( T /K). The other thermodynamic quantities of the Association process were also calculated and show that the driving force for the ion Association reaction is the Association entropy.

Pengsheng Song - One of the best experts on this subject based on the ideXlab platform.

  • thermodynamics of ionic Association 1 the standard Association Constant of the ion pair li b oh 4
    Thermochimica Acta, 2000
    Co-Authors: Jiazhen Yang, Bai Sun, Pengsheng Song
    Abstract:

    Abstract Values of emf for the cell without liquid junction Pt, H 2 (101.325 kPa) |Li 2 B 4 O 7 ( m 1 ), LiCl ( m 2 )|AgCl–Ag are reported at five temperatures from 278.15 to 318.15 K. The standard Association Constant of ionic pair Li + B(OH) 4 − , K a , is determined by a fitting with the cell results. The dependence of p K a on temperature T is expressed in empirical equation: p K a =−131.6 K / T −0.08996−1.856×10 −3 T / K . The other thermodynamic quantities of the Association process are calculated and show that there truly exists ion pair Li + B(OH) 4 − and the driving force for the ion Association reaction is Association entropy.

  • thermodynamic study of aqueous borates iii the standard Association Constant of the ion pair li b oh 4
    The Journal of Chemical Thermodynamics, 1997
    Co-Authors: Jiazhen Yang, Pengsheng Song, Dongbao Wang
    Abstract:

    Abstract Values of e.m.f. for the cell without liquid junction: Pt H 2 ( p = 101.325kPa)|K 2 B 4 0 7 ( m 1 ) LiCl( m 2 )|AgCl Ag are reported at seven Constant ionic strengths from 0.07 to 2.0 mol·kg −1 at five temperatures from 278.15 K to 318.15 K. The standard Association Constant K a of the ionic pair Li + B(OH) 4 − , is determined by a fit with the cell results. The dependence of p K a on temperature T is expressed by the empirical equation: p K a = −149.8(K/ T ) + 0.09024 − 2.112·10 −3 ( T /K). The other thermodynamic quantities of the Association process were also calculated and show that the driving force for the ion Association reaction is the Association entropy.

Dongbao Wang - One of the best experts on this subject based on the ideXlab platform.

  • thermodynamic study of aqueous borates iii the standard Association Constant of the ion pair li b oh 4
    The Journal of Chemical Thermodynamics, 1997
    Co-Authors: Jiazhen Yang, Pengsheng Song, Dongbao Wang
    Abstract:

    Abstract Values of e.m.f. for the cell without liquid junction: Pt H 2 ( p = 101.325kPa)|K 2 B 4 0 7 ( m 1 ) LiCl( m 2 )|AgCl Ag are reported at seven Constant ionic strengths from 0.07 to 2.0 mol·kg −1 at five temperatures from 278.15 K to 318.15 K. The standard Association Constant K a of the ionic pair Li + B(OH) 4 − , is determined by a fit with the cell results. The dependence of p K a on temperature T is expressed by the empirical equation: p K a = −149.8(K/ T ) + 0.09024 − 2.112·10 −3 ( T /K). The other thermodynamic quantities of the Association process were also calculated and show that the driving force for the ion Association reaction is the Association entropy.

V Ramakrishnan - One of the best experts on this subject based on the ideXlab platform.

  • determination of Association Constant of host guest supramolecular complex molecular recognition of carbamazepine antiseizure drug with calix 4 arene
    Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2015
    Co-Authors: C Meenakshi, P Jayabal, V Ramakrishnan
    Abstract:

    Abstract The thermodynamic property of the host–guest, inclusion complex formed between p - t -butyl calix(4)arene which is a supramolecule, and the antiseizure drug, carbamazepine was studied. p - t -Butyl calix(4)arene has been used as a host molecule and carbamazepine as a guest molecule. Optical absorption spectral studies were carried out to investigate the molecular recognition properties of p - t -butyl calix(4)arene with carbamazepine. The stochiometry of the host–guest complexes formed and the Association Constant were determined. An interesting 1:2 stochiometric host–guest complex was formed. Job’s continuous method of variation and Benesi–Hildebrand expression were used for the determination of binding Constant and the stochiometry of the host–guest complex formed. Molecular dimension of the host molecule plays a vital role in the formation of the host–guest stochiometric complexes.

Jie Wang - One of the best experts on this subject based on the ideXlab platform.

  • thermodynamics of ion pairs in mixed solvents i the standard Association Constant of the ion pair mgso4 oin 0 03226 co nh2 2 0 96774 h2o
    The Journal of Chemical Thermodynamics, 2001
    Co-Authors: Jiazhen Yang, Rubo Zhang, Hong Liu, Jie Wang
    Abstract:

    Abstract The standard potential of the (Ag, AgCl) electrode E o , the standard second ionization Constant of sulfuric acid K 2 , and the standard Association Constant of the ion pair [MgSO 4 ] o , K in {0.03226 CO(NH 2 ) 2  +  0.96774 H 2 O } at five temperatures from 278.15 K to 318.15 K were determined from precise e.m.f. measurements of different cells without liquid junction. The dependence of p K on temperature T is expressed by the empirical equation p K  =  6.617  −  777.9 · ( K  /  T )  −  0.02001 · ( T  /  K ). The other thermodynamic functions of the Association process were also calculated and show that the driving force for the process is the entropy of Association.