Matches in UGent Biblio for { <https://biblio.ugent.be/publication/181292#aggregation> ?p ?o. }
Showing items 1 to 34 of
34
with 100 items per page.
- aggregation classification "A1".
- aggregation creator B30957.
- aggregation creator person.
- aggregation creator person.
- aggregation date "1996".
- aggregation format "application/pdf".
- aggregation hasFormat 181292.bibtex.
- aggregation hasFormat 181292.csv.
- aggregation hasFormat 181292.dc.
- aggregation hasFormat 181292.didl.
- aggregation hasFormat 181292.doc.
- aggregation hasFormat 181292.json.
- aggregation hasFormat 181292.mets.
- aggregation hasFormat 181292.mods.
- aggregation hasFormat 181292.rdf.
- aggregation hasFormat 181292.ris.
- aggregation hasFormat 181292.txt.
- aggregation hasFormat 181292.xls.
- aggregation hasFormat 181292.yaml.
- aggregation isPartOf urn:issn:0022-0248.
- aggregation language "eng".
- aggregation rights "I have transferred the copyright for this publication to the publisher".
- aggregation subject "Chemistry".
- aggregation title "Influence of the solution composition on the stoichiometry of Na+- and of K+-containing carbonated apatites obtained by the hydrolysis of monetite".
- aggregation abstract "In this study, Na+- and CO32--containing hydroxyapatites (NCAps) and K+- and CO32-- containing hydroxyapatites (KCAps) were prepared by the hydrolysis of monetite in solutions with independently varied CO32- and alkalimetal (M(+)) concentration. The chemical and physical analysis results show that both the CO32- and the M(+) incorporation in apatite can affect the dimensions of the hexagonal lattice. From the composition of the unit cell of these apatites, the contributions of the substitution mechanisms for the incorporation of CO32- and M(+) could be calculated. Generally, the contributions of the predominant mechanisms, (Ca2++PO43-+OH-<->V-Ca+CO32-+V-OH) and (Ca2++PO43-<->M(+)+CO32-) with V-X a vacancy on a regular X lattice site, vary as can be expected on the basis of the variation of the driving force in the hydrolysis solution. Their behavior seems to suppress the appearance of the less stable mechanisms: (Ca2++OH-<->M(+)+V-OH) for the NCAps and (Ca2++2PO(4)(3-)<->V-Ca+2CO(3)(2-)) for the KCAps. This suggests that, although there is no intrinsic coupling between the fundamental substitution mechanisms, an indirect correlation can occur.".
- aggregation authorList BK78469.
- aggregation endPage "547".
- aggregation issue "3".
- aggregation startPage "539".
- aggregation volume "169".
- aggregation aggregates 1053376.
- aggregation isDescribedBy 181292.
- aggregation similarTo S0022-0248(96)00424-1.
- aggregation similarTo LU-181292.