期刊
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 17, 期 21, 页码 13882-13894出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cp00552c
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资金
- Compagnia di San Paolo
- University of Turin [ORTO114XNH]
- European COST Action [MP1202]
We report the synthesis and surface functionalization of MCM-41-like mesoporous silica nanoparticles (MSNs) with spheroidal shape and particle size of 141 +/- 41 nm. The success of surface functionalization with aminopropyl and sodium ethylcarboxylate groups (giving amino-MSN and carboxy-MSN, respectively) was ascertained by infrared spectroscopy and zeta potential measurements. The former showed the decrease of surface silanol groups and the corresponding appearance of signals related to NH2 bending mode (delta NH2) at 1595 cm(-1) and COO stretching (v(as) and v(sym)) at 1562 and 1418 cm(-1). The latter showed a change in surface charge, in that the isoelectric point (IEP) changed from pH 3-4.5 to 8.5 when the MSN was functionalized with the amino groups, while carboxy-MSN showed a more negative charge in the whole pH range with respect to MSN. The hydrophilic character of the prepared materials was ascertained by quantitative microgravimetric measurements, allowing the calculation of the average isosteric adsorption heat ((q) over bar (st)). This was found to be 51 +/- 3 kJmol(-1), 61 +/- 4, and 65 +/- 3 kJmol(-1) for MSN, amino-MSN, and carboxy-MSN samples, respectively. The increase in (q) over bar (st) after functionalization can be ascribed to the specific interaction of water molecules with the functionalizing agents, in agreement with a higher basicity with respect to silanol groups. Moreover, the possibility of multiple H-bonding interactions of water molecules with the carboxylate anion is put forward to account for the higher water uptake with respect to parent MSN.
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