scholarly journals Adsorption of the Tartrate Ions in the Hydroxyapatite/Aqueous Solution of NaCl System

Materials ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 3039
Author(s):  
Władysław Janusz ◽  
Ewa Skwarek

The research on the interaction of tartrate ions with the surface of hydroskyapatite was presented, including the measurements of the kinetics of tartrate ion adsorption and tartrate ion adsorption as a function of pH. The adsorption of tartrate ions was calculated from the loss of tartrate concentration in the solution as measured by a radioisotope method using C-14 labeled tartaric acid. In order to explain the mechanism of interaction of tartrate ions with hydroxyapatite, supplementary measurements were carried out, i.e., potentiometric measurements of the balance of released/consumed ions in the hydroxyapatite/electrolyte solution system, zeta potential measurements, FTIR spectrophotometric measurements and the hydroxyapatite crystal structure and particle size distribution were characterized. It was found that the adsorption of tartrate ions occurs as a result of the exchange of these ions with hydroxyl, phosphate and carbonate ions. Replacing the ions with the abovementioned tartrate ions leads to the appearance of a negative charge on the surface of the hydroxapatite. On the basis of XRD study and particle size distribution, a decrease in the size of crystallites and the diameter of hydroxyapatite particles in contact with a solution of 0.001 mol/dm3 of tartaric acid was found.

Author(s):  
Li Bao ◽  
Ting-an Zhang ◽  
Weimin Long ◽  
Anh V. Nguyen ◽  
Guozhi Lv ◽  
...  

2010 ◽  
Vol 638-642 ◽  
pp. 3925-3930 ◽  
Author(s):  
K.G. Wang ◽  
X. Ding

The dynamics of phase coarsening at ultra-high volume fractions is studied based on two-dimensional phase-field simulations by numerically solving the time-dependent Ginzburg-Landau and Cahn-Hilliard equations. The kinetics of phase coarsening at ultra-high volume fractions is discovered. The microstructural evolutions for different ultra-high volume fractions are shown. The scaled particle size distribution as functions of the dispersoid volume fraction is presented. The particle size distribution derived from our simulation at ultra-high volume fractions is close to Wagner's particle size distribution due to interface-controlled ripening rather than Hillert's grain size distribution in grain growth. The changes of shapes of particles are carefully studied with increase of volume fraction. It is found that more liquid-filled triple junctions are formed as a result of particle shape accommodation with increase of volume fraction at the regime of ultra-high volume fraction.


2019 ◽  
Vol 120 (4) ◽  
pp. 345-352
Author(s):  
X. R. Zhou ◽  
Y. S. Li ◽  
Z. L. Yan ◽  
C. W. Liu ◽  
L. H. Zhu

1983 ◽  
Vol 28 ◽  
Author(s):  
R.D. Kissinger ◽  
S.V. Nair ◽  
J.K. Tien

ABSTRACTThe kinetics of powder consolidation, or densification, and the powder morphological changes ocurring during hot isostatic pressing (HIP) are studied as a function of particle size distribution and hold time at HIP temperature for the nickel base superalloy RENE-95. In order to understand the extent of individual powder particle deformation during consolidation and its effect on subsequent prior particle boundaries (PPB), particle size distribution was studied as a variable. Particle size distributions studied include monosized (75–90 um), bimodal ( 75–90 um and 33–35 um) and commercial (<104 um) size distributions. The experimental results of HIP densification kinetics are compared with a newly developed analytical deformation mechanism model for HIP consolidaiton which takes into account the effect of a distribution of particle sizes on the kinetics of densification.


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