An XPS study of the dissolution kinetics of chrysotile in 0.1 N oxalic acid at different temperatures

1977 ◽  
Vol 1 (4) ◽  
pp. 385-398 ◽  
Author(s):  
J. H. Thomassin ◽  
J. Goni ◽  
P. Baillif ◽  
J. C. Touray ◽  
M. C. Jaurand
Keyword(s):  
Oxalic Acid ◽  
Dissolution Kinetics ◽  
Different Temperatures ◽  
Xps Study ◽  
Kinetics Of

Characterization of Type B Carbonate Apatite Sintered Bodies

2011 ◽  
Vol 1301 ◽  
Author(s):  
N. Watanobe ◽  
T. Yoshioka ◽  
T. Ikoma ◽  
T. Kuwayama ◽  
T. Higaki ◽  
...  
Keyword(s):  
Dissolution Kinetics ◽  
Carbonate Apatite ◽  
Artificial Bone ◽  
Type B ◽  
Desorption Process ◽  
Different Temperatures ◽  
Acidic Conditions ◽  
Kinetics Of ◽  
Potential Use

ABSTRACTThe dissolution kinetics of type B carbonate apatite (CAp) disks sintered at different temperatures were investigated under acidic conditions similar to an osteoclastic desorption process in bone remodeling. The type B CAp disks, which were uniaxially pressed at 98MPa and sintered at temperatures of 600 to 700 ºC, showed single crystalline phase and a high relative density of 60-62 % compared to the stoichiometric density of 3.16g/cm3 of hydroxyapatite (HAp). The dissolution rate of type B CAp disks sintered at 650 ºC was 3.5 times faster than that of HAp disks at 650 ºC. These results indicate that the Type B CAp sintered disks show potential use as a biodegradable material for artificial bone.

scholarly journals Application of the Shrinking-Core Models for Determination of Dissolution Kinetics of Mn and Zn from Spent Zinc–Carbon Battery Powder in Organic Acid Solution

2019 ◽  
Vol 27 (1) ◽  
pp. 99-109 ◽  
Author(s):  
Tevfik Agacayak ◽  
Hasan Ali Taner
Keyword(s):  
Acetic Acid ◽  
Acid Solution ◽  
Acetic Acid Solution ◽  
Dissolution Kinetics ◽  
Kinetic Studies ◽  
Product Layer ◽  
Different Temperatures ◽  
Shrinking Core ◽  
Kinetics Of Dissolution ◽  
Kinetics Of

Abstract In this study, dissolution kinetics of manganese and zinc from spent zinc–carbon batteries in acetic acid solution was investigated. To determine the kinetics of dissolution of manganese and zinc, shrinking core model was applied to dissolution recoveries obtained at different temperatures. As a result of kinetic studies, it was determined that manganese and zinc were dissolved in acetic acid solution by diffusion from product layer and then activation energies (Ea) were calculated.

Influence of oxalic acid on the dissolution kinetics of manganese oxide

2012 ◽  
Vol 2012 (11) ◽  
pp. 935-941 ◽  
Author(s):  
E. B. Godunov ◽  
I. V. Artamonova ◽  
I. G. Gorichev ◽  
Yu. A. Lainer
Keyword(s):  
Oxalic Acid ◽  
Manganese Oxide ◽  
Dissolution Kinetics ◽  
Kinetics Of

scholarly journals Kinetics of dissolution of calcium phosphate (Ca-P) bioceramics

2008 ◽  
Vol 2 (1) ◽  
pp. 57-62 ◽  
Author(s):  
Lukas Brazda ◽  
Dana Rohanova ◽  
Ales Helebrant
Keyword(s):  
Calcium Phosphate ◽  
Dissolution Rate ◽  
Dissolution Kinetics ◽  
Weight Changes ◽  
Enhanced Dissolution ◽  
Different Temperatures ◽  
Sbf Solution ◽  
Kinetics Of Dissolution ◽  
Unexpected Findings ◽  
Kinetics Of

Hydroxyapatite (HAp) and ?-tricalcium phosphate (?-TCP) are widely used bioceramics for surgical or dental applications. This paper is dealing with dissolution kinetics of synthetically prepared ?-TCP and four types of HAp granules. Two groups of HAp, treated at different temperatures, each of them with two different granule sizes, were tested. Three corrosive solutions with different pH and simulated body fluid (SBF) were used for immersing of the samples. Changes in concentrations of calcium and phosphate ions, pH level and weight changes of the samples were observed. It was found that presence of TRIS buffer enhanced dissolution rate of the ?-TCP approximately two times. When exposed to SBF solution, calcium phosphate (most probably hydroxyapatite) precipitation predominates over ?-TCP dissolution. Results from HAp samples dissolution showed some unexpected findings. Neither heat treatment nor HAp particle size made any major differences in dissolution rate of the same mass of each HAp sample.

Comparative Labelling and Biokinetic Studies of 99mTc-EDTA(Sn) and 99mTc-DTPA(Sn)

1977 ◽  
Vol 16 (01) ◽  
pp. 30-35 ◽  
Author(s):  
N. Agha ◽  
R. B. R. Persson
Keyword(s):  
Complex Formation ◽  
Significant Influence ◽  
Room Temperature ◽  
Ph Value ◽  
Maximum Activity ◽  
Reduction Step ◽  
Labelling Yield ◽  
Different Temperatures ◽  
Kinetics Of

SummaryGelchromatography column scanning has been used to study the fractions of 99mTc-pertechnetate, 99mTcchelate and reduced hydrolyzed 99mTc in preparations of 99mTc-EDTA(Sn) and 99mTc-DTPA(Sn). The labelling yield of 99mTc-EDTA(Sn) chelate was as high as 90—95% when 100 μmol EDTA · H4 and 0.5 (Amol SnCl2 was incubated with 10 ml 99mTceluate for 30—60 min at room temperature. The study of the influence of the pH-value on the fraction of 99mTc-EDTA shows that pH 2.8—2.9 gave the best labelling yield. In a comparative study of the labelling kinetics of 99mTc-EDTA(Sn) and 99mTc- DTPA(Sn) at different temperatures (7, 22 and 37°C), no significant influence on the reduction step was found. The rate constant for complex formation, however, increased more rapidly with increased temperature for 99mTc-DTPA(Sn). At room temperature only a few minutes was required to achieve a high labelling yield with 99mTc-DTPA(Sn) whereas about 60 min was required for 99mTc-EDTA(Sn). Comparative biokinetic studies in rabbits showed that the maximum activity in kidneys is achieved after 12 min with 99mTc-EDTA(Sn) but already after 6 min with 99mTc-DTPA(Sn). The long-term disappearance of 99mTc-DTPA(Sn) from the kidneys is about five times faster than that for 99mTc-EDTA(Sn).

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