Adsorbent calcium hydroxyapatite

The value of for calcium hydroxyapatite can be defined by charge of Ca + and PO ions. From this point of view calcium hydroxyapatite can be used as high-selective adsorbents for high performance liquid chromatography because with increasing of will be rise a selectivity coefficient a. 

The potential of other nuclei for the study of surfaces is yet to be explored. Gottlieb and Luz (388) measured 2H spectra of a number of perdeuterated molecules adsorbed on active alumina and interpreted the results in terms of quadrupolar tensors. Yesinowski and Mobley (369) have shown that 19F MAS NMR can provide useful information about fluorinated surfaces of calcium hydroxyapatite, Cas(0H)(P04)3. In particular, l9F, 2H, and H MAS NMR may become powerful techniques for the study of interface systems in general. 

Calcium hydroxyapatite is an interesting adsorbent which collects cations of heavy metals such as lead and cadmium. Suzuki (1985) suggested that hydroxyapatite is capable of ion exchange not only with... 

Precipitation can occur if a water is supersaturated with respect to a solid phase however, if the growth of a thermodynamically stable phase is slow, a metastable phase may form. Disordered, amorphous phases such as ferric hydroxide, aluminum hydroxide, and allophane are thermodynamically unstable with respect to crystalline phases nonetheless, these disordered phases are frequently found in nature. The rates of crystallization of these phases are strongly controlled by the presence of adsorbed ions on the surfaces of precipitates (99). Zawacki et al. (Chapter 32) present evidence that adsorption of alkaline earth ions greatly influences the formation and growth of calcium phosphates. While hydroxyapatite was the thermodynamically stable phase under the conditions studied by these authors, it is shown that several different metastable phases may form, depending upon the degree of supersaturation and the initiating surface phase. 

Only a few systematic studies have been carried out on the mechanism of interaction of organic surfactants and macromolecules. Mishra et al. (12) studied the effect of sulfonates (dodecyl), carboxylic acids (oleic and tridecanoic), and amines (dodecyl and dodecyltrimethyl) on the electrophoretic mobility of hydroxyapatite. Vogel et al. (13) studied the release of phosphate and calcium ions during the adsorption of benzene polycarboxylic acids onto apatite. Jurlaanse et al.(14) also observed a similar release of calcium and phosphate ions during the adsorption of polypeptides on dental enamel. Adsorption of polyphosphonate on hydroxyapatite and the associated release of phosphate ions was investigated by Rawls et al. (15). They found that phosphate ions were released into solution in amounts exceeding the quantity of phosphonate adsorbed. 

The adsorption of amino acids on rutile and hydroxyapatite exhibits some characteristics of specific adsorption. The results can be interpreted in terms of electrostatic models of adsorption, however, if reorientation of adsorbed molecules is taken into consideration. The electrokinetic behavior of hydroxyapatite in glutamic acid is complicated because of a chemical reaction, possibly involving calcium ions. The study shows that it is necessary to take into consideration the orientation of adsorbed molecules, particularly for zwitterionic surfactants. 

Recently, Bartels and Arends113 studied the adsorption of poly(4-vinylpyridinium fluoride) with different hexadecyl group content on hydroxyapatite. Adsorbance decreased as the hexadecyl content, i.e. the charge density, was increased. Desorption experiments showed that the adsorption of this polyelectrolyte in water is essentially irreversible. However, the polymer partially desorbed when excess calcium ions were added. Bartels and Arends concluded that adsorption of poly(4-vinylpyridinum fluoride) occurs as a result of the uptake of fluoride ions by hydroxyapatite which releases phosphate ions into water. They also suggested that this adsorption phenomenon can be interpreted in terms of an ion-exchange mechanism. 

Adsorption This method is the simplest way to immobilize enzymes. Enzymes can be adsorbed physically on a surface-active adsorbent by contacting an aqueous solution of enzyme with an adsorbent. Commonly employed adsorbents are (Zaborsky, 1973) alumina, amon-exchange resins, calcium carbonate, carbon, cation-exchange resins, celluloses, clays, collagen, colloid-ion, conditioned metal, glass plates, diatomaceous earth, and hydroxyapatite. The advantages of adsorption techniques are as follows ... 

The data in Table IV for the three samples of hydroxyapatite summarize the range for shifts in these samples of hydroxyapatite. Shifts have not been observed in commercially available hydroxyapatites, one sample of natural apatite, or calcium phosphates. Likewise, calcium phosphates prepared by methods which yield high specific surface have also not responded in this manner to adsorbates. 

We wish to report some work on the adsorption of acid and alkali-precursor gelatins, the water-soluble products of collagen. The study of both types allowed us to determine whether the differences exhibited by the two kinds in solution are reflected in the adsorbed state, and offers some insight into the state of flexible molecules at interfaces. The use of two dissimilar adsorbents, glass and stainless steel powders, should yield information on segment-surface interactions during the adsorption process. Some effects of added calcium ions were also studied since the Ca-ions of hydroxyapatite in bone and teeth are intimately related to collagen. 

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