In nanosized pores, liquid water can be thermodynamically stable down to temperatures well below the limit of homogeneous nucleation of bulk water ( approximately 235 K). Studies of water in such pores therefore offer an opportunity to reveal the anomalous behavior of deeply supercooled water. Herein we focus on recent studies of the limits of freezing and melting of water in the cylindrical pores of ordered mesoporous silicas with pore diameters in the range of 2-10 nm, based on vapor sorption measurements, calorimetric studies, NMR spectroscopy and cryoporometry, and neutron diffraction studies.

Organic coatings based on inhibitor loaded inorganic containers for smart corrosion inhibition are presented. The overall coating performance is strongly infl uenced by the containers as well as their inhibitor capacity, compatibility with the coating matrix, and size. The important effect of container size is described for the fi rst time in this work by investigating two types of mesoporous silica containers of different diameters: 80 and 700 nm. The coating physical properties (thickness and adhesion) are comparable for both container types. In contrast, the coating barrier properties are strongly infl uenced by the container size as assessed with electrochemical impedance spectroscopy (EIS). The incorporation of bigger containers reduces the coating resistance by a factor of two. Surprisingly, despite the similar amounts (20 wt%) of loaded inhibitor (2-mercaptobenzothiazole), different active inhibition ability is detected with the scanning vibrating electrode technique (SVET). Therefore, it is found that coatings with smaller containers exhibit better self-healing performance.

MCM-41 and SBA-15 silicas were studied by (29)Si solid-state NMR and (15)N NMR in the presence of (15)N-pyridine with the aim to formulate generic structural parameters that may be used as a checklist for atomic-scale structural models of this class of ordered mesoporous materials. High-quality MCM-41 silica constitutes quasi-ideal arrays of uniform-size pores with thin pore walls, while SBA-15 silica has thicker pore walls with framework and surface defects. The numbers of silanol (Q(3)) and silicate (Q(4)) groups were found to be in the ratio of about 1:3 for MCM-41 and about 1:4 for our SBA-15 materials. Combined with the earlier finding that the density of surface silanol groups is about three per nm(2) in MCM-41 (Shenderovich, et al. J. Phys. Chem. B 2003, 107, 11924) this allows us to discriminate between different atomic-scale models of these materials. Neither tridymite nor edingtonite meet both of these requirements. On the basis of the hexagonal pore shape model, the experimental Q(3):Q(4) ratio yields a wall thickness of about 0.95 nm for MCM-41 silica, corresponding to the width of ca. four silica tetrahedra. The arrangement of Q(3) groups at the silica surfaces was analyzed using postsynthesis surface functionalization. It was found that the number of covalent bonds to the surface formed by the functional reagents is affected by the surface morphology. It is concluded that for high-quality MCM-41 silicas the distance between neighboring surface silanol groups is greater than 0.5 nm. As a result, di- and tripodical reagents like (CH(3))(2)Si(OH)(2) and CH(3)Si(OH)(3) can form only one covalent bond to the surface. The residual hydroxyl groups of surface-bonded functional reagents either remain free or interact with other reagent molecules. Accordingly, the number of surface silanol groups at a given MCM-41 or SBA-15 silica may not decrease but increase after treatment with CH(3)Si(OH)(3) reagent. On the other hand, nearly all surface silanol groups could be functionalized when HN(Si(CH(3))(3))(2) was used.

The hydrogen bond interaction of pyridine with sulfonic and phosphonic acid moieties at the surface of SBA-15 ordered mesoporous silica has been studied by a combination of solid-state NMR techniques. The composition of the materials is characterized by 29Si MAS NMR, the residual water content is inspected by 1H MAS NMR, and the hydrogen bond interactions are characterized by 15N CPMAS NMR at 130 K using pyridine-15 N as a probe molecule. It is shown that (i) all acid moieties at the surface are accessible for pyridine; (ii) each sulfonic acid moiety interacts with one pyridine molecule; (iii) each phosphonic acid moiety can interact simultaneously with two pyridine molecules; (iv) for both materials the interaction of the acid moieties with the base results in proton transfer to pyridine. The observed proton-donating ability of the acid moieties depends on the presence of residual water. In contrast to nonfunctionalized SBA-15, the sulfonic acid-functionalized SBA-15 material contains about six water molecules per acid moiety after drying at 420 K in high vacuum. From the 15N chemical shift of pyridine in the hydrogen-bonded complex, it is estimated that the proton-donating ability of the acidic functional groups solvated by such small water clusters is equivalent to that of acids in water exhibiting a pK a of about 0.6 and 1.3, respectively, for the sulfonic and phosphonic acid moieties. The O···H and H···N distances in the hydrogen bond of the pyridine complex are r OH ≈ 1.69 Å and r HN ≈ 1.05 Å for sulfonic acid, as compared to r OH ≈ 1.53 Å and r HN ≈ 1.09 Å for phosphonic acid.