Surface chemical functionalities in bioactive glasses. The gas/solid adsorption of acetonitrile

被引:23
作者
Cerruti, M
Bolis, V
Magnacca, G
Morterra, C
机构
[1] Univ Turin, Dept Chem IFM, I-10125 Turin, Italy
[2] Univ Turin, Res Unit, Consortium INSTM, I-10125 Turin, Italy
[3] Univ Piemonte Orientale, DiSCAFF, I-28100 Novara, Italy
[4] Consortium INSTM, Res Unit Piemonte Orientale, I-28100 Novara, Italy
关键词
D O I
10.1039/b315418a
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
The room temperature adsorption of acetonitrile (ACN) on two sol-gel glassy systems for biomedical applications (58S and 77S; composition: SiO2-CaO-P2O5) was studied by in situ IR spectroscopy/adsorption microcalorimetry, and the influence of the chemical composition on the surface properties of the glasses was investigated. In order to highlight the role played by Ca and P species in modifying the surface properties of a silica matrix, some model systems were also investigated, namely: (i) a pure commercial amorphous silica; (ii) the same silica system, surface modified with dosed amounts of Ca and/or P species. Different effects were observed, depending on the metal (Ca) or non-metal (P) nature of the hetero-atoms. The contact of (perdeuterated) ACN with Ca surface species yielded a nu(CN) IR band at similar to2185 cm(-1), assigned to Ca2+ <-- NCA coordinative interactions. The spectral position of the nu(CN) band is independent of the sample origin (either bioactive glass or Ca-doped silica), whereas population and energy distribution of the species formed depend (strongly) on both sample origin and Ca loading. Surface acidic properties of all systems increase significantly with Ca content, as witnessed by both adsorbed amounts and adsorption enthalpies. The zero-coverage values of the latter quantity are quite high for the 58S and 77S bioactive glasses (similar to95 and similar to80 kJ mol(-1), respectively) and for medium-high Ca-loaded silicas (similar to80 and > 100 kJ mol(-1) for 8 and 16% CaO, respectively). ACN adsorption enthalpy on surface SiOH groups is close to/lower than the enthalpy of ACN liquefaction (30 kJ mol(-1)). In the case of the highest Ca surface loading, the increased ionic nature of the system induces a significant surface reactivity, never observed in the case of bioactive glasses. By contrast, P species do not affect significantly the surface acid/base properties of all silica-based systems, especially when Ca species are present also (in excess).
引用
收藏
页码:2468 / 2479
页数:12
相关论文
共 43 条
[1]   IR STUDY OF ACETONITRILE ADSORPTION ON HYDROXYLATED ZIRCONIUM DIOXIDE - MECHANISM OF ACETONITRILE HYDROLYSIS [J].
ABOULAYT, A ;
BINET, C ;
LAVALLEY, JC .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1995, 91 (17) :2913-2920
[2]   THE DETERMINATION OF PORE VOLUME AND AREA DISTRIBUTIONS IN POROUS SUBSTANCES .1. COMPUTATIONS FROM NITROGEN ISOTHERMS [J].
BARRETT, EP ;
JOYNER, LG ;
HALENDA, PP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (01) :373-380
[3]   HYDROPHILIC AND HYDROPHOBIC SITES ON DEHYDRATED CRYSTALLINE AND AMORPHOUS SILICAS [J].
BOLIS, V ;
FUBINI, B ;
MARCHESE, L ;
MARTRA, G ;
COSTA, D .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1991, 87 (03) :497-505
[4]   Calorimetric and IR spectroscopic study of the interaction of NH3 with variously prepared defective silicalites -: Comparison with ab initio computational data [J].
Bolis, V ;
Busco, C ;
Bordiga, S ;
Ugliengo, P ;
Lamberti, C ;
Zecchina, A .
APPLIED SURFACE SCIENCE, 2002, 196 (1-4) :56-70
[5]   X-ray photoelectron spectroscopy and x-ray absorption near edge structure study of copper sites hosted at the internal surface of ZSM-5 zeolite:: A comparison with quantitative and energetic data on the CO and NH3 adsorption [J].
Bolis, V ;
Maggiorini, S ;
Meda, L ;
D'Acapito, F ;
Palomino, GT ;
Bordiga, S ;
Lamberti, C .
JOURNAL OF CHEMICAL PHYSICS, 2000, 113 (20) :9248-9261
[6]   Structural controls on the solubility of CO2 in silicate melts Part II:: IR characteristics of carbonate groups in silicate glasses [J].
Brooker, RA ;
Kohn, SC ;
Holloway, JR ;
McMillan, PF .
CHEMICAL GEOLOGY, 2001, 174 (1-3) :241-254
[7]   Adsorption of gases in multimolecular layers [J].
Brunauer, S ;
Emmett, PH ;
Teller, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 :309-319
[8]  
Burneau A, 1998, SURFACE PROPERTIES OF SILICAS, P147
[9]   INFRARED SPECTROSCOPIC IDENTIFICATION OF SPECIES ARISING FROM REACTIVE ADSORPTION OF CARBON OXIDES ON METAL-OXIDE SURFACES [J].
BUSCA, G ;
LORENZELLI, V .
MATERIALS CHEMISTRY, 1982, 7 (01) :89-126
[10]   Spectroscopic characterization of the acid properties of metal oxide catalysts [J].
Busca, G .
CATALYSIS TODAY, 1998, 41 (1-3) :191-206