Hydroxyapatite organofunctionalized with silylating agents to heavy cation removal

被引:56
作者
da Silva, Oberto G.
da Silva Filho, Edson C.
da Fonseca, Maria G. [1 ]
Arakaki, Luiza N. H.
Airoldi, Claudio
机构
[1] Univ Fed Paraiba, Dept Quim, CCEN, BR-58059900 Joao Pessoa, Paraiba, Brazil
[2] Univ Estadual Campinas, Inst Quim, BR-13084971 Sao Paulo, Brazil
关键词
organofunctionalization; alkoxysilanes; adsorption; hydroxyapatite;
D O I
10.1016/j.jcis.2006.07.010
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hydroxyapatite surface silylation with organosilane derivatives (H(3)CObSiR, R being the corresponding organic moieties -CH2CH2CH2NH,), -CH2CH2CH2NHCH2CH2NH2, and -CH2CH2CH2NHCH2CH2NHCH2CH2NH2, was carried out to yield organofunctionalized nanomaterials, named HApR1, HApR2. and HApR3, respectively. The products were characterized by elemental analysis, infrared spectroscopy, X-ray diffraction. thermogravimetry, and P-31 and C-13 NMR in the solid state. The amounts of groups grafted onto surfaces were 0.75 +/- 0.05, 2.35 +/- 0.14, and 2.48 +/- 10.18 mmol g(-1) for HApRx (x = 1,2, 3) surfaces, respectively. Linear correlations between elemental analysis, mass loss, 31 p chemical shift data, and the characteristics of the chain of each alkoxysilane were observed. The organic basic centers distributed onto the external surface have the ability to adsorb divalent copper and cobalt cations from aqueous solution. The degree of adsorption obtained from batchwise processes showed the best performance of these synthesized nanomaterials when compared with the pristine hydroxyapatite. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:485 / 491
页数:7
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