Department of Chemistry and Biochemistry, Seton Hall University, South Orange, NJ 07079, USA.
J Colloid Interface Sci. 2011 Apr 15;356(2):690-8. doi: 10.1016/j.jcis.2011.01.033. Epub 2011 Jan 21.
This work describes adsorption and wetting characterization of hydrophobic ordered mesoporous silicas (OMSs) with the SBA-15 motif. Three synthetic approaches to prepare hydrophobic SBA-15 silicas were explored: grafting with (1) covalently-attached monolayers (CAMs) of C(n)H(2)(n+1)Si(CH(3))(2)N(CH(3))(2), (2) self-assembled monolayers (SAMs) of C(n)H(2)(n+1)Si(OEt)(3), and (3) direct ("one-pot") co-condensation of TEOS with C(n)H(2)(n+1)Si(OEt)(3) in presence of P123 (n=1-18). The materials prepared were characterized by nitrogen adsorption, TEM, and chemical analysis. The surface properties of the materials were assessed by water contact angles (CAs) and by BET C constants. The results showed that, while loadings of the alkyl groups (%C) were comparable, the surface properties and pore ordering of the materials prepared through different methods were quite different. The best quality hydrophobic surfaces were prepared for SBA-15 grafted with CAMs of alkylsilanes. For these materials, the water CAs were above ∼120°/100° (adv/rec) and BET C constants were in the range of ∼15-25, indicating uniform low-energy surfaces of closely packed alkyl groups on external and internal surfaces of the pores respectively. Moreover, surfaces grafted with the long-chained (C(12)-C(18)) silanes showed super-hydrophobic behavior (CAs∼150-180°) and extremely low adhesion for water. The pore uniformity of parental SBA-15 was largely preserved and the pore volume and pore diameter were consistent with the formation of a single layer of alkylsilyl groups inside the pores. Post-synthesis grafting of SBA-15 with SAMs worked not as well as CAMs: the surfaces prepared demonstrated lower water CAs and higher BET C constants, thereby indicating a small amount of accessible polar groups (Si-OH) related to packing constrains for SAMs supported on highly curved surfaces of mesopores. The co-condensation method produced substantially more disordered materials and less hydrophobic surfaces than any of the grafting methods. The surfaces of these materials showed low water CAs and high BET C constants (∼100-200) thereby demonstrating a non-uniform surface coverage and presence of unmodified silica. It is concluded that CAMs chemistry is the most efficient approach in preparation of the functionalized OMS materials with uniform surfaces and pores.
本文描述了具有 SBA-15 结构的疏水有序介孔硅(OMS)的吸附和润湿特性。探索了三种合成疏水 SBA-15 硅的方法:(1)通过共价键接枝(C(n)H(2)(n+1)Si(CH(3))(2)N(CH(3))(2)的单层(CAMs),(2)通过自组装单层(SAMs)的 C(n)H(2)(n+1)Si(OEt)(3),以及(3)在 P123 存在下直接(“一锅法”)共缩合 TEOS 和 C(n)H(2)(n+1)Si(OEt)(3)。通过氮吸附、TEM 和化学分析对制备的材料进行了表征。通过水接触角(CA)和 BET C 常数评估了材料的表面性质。结果表明,尽管烷基基团的负载量(%C)相当,但通过不同方法制备的材料的表面性质和孔有序性却大不相同。用烷基硅烷的 CAM 接枝的 SBA-15 制备出了质量最好的疏水表面。对于这些材料,水 CA 大于约 120°/100°(adv/rec),BET C 常数在约 15-25 的范围内,表明分别在孔的内外表面上紧密堆积的烷基基团具有均匀的低能表面。此外,用长链(C(12)-C(18))硅烷接枝的表面表现出超疏水性(CA 约为 150-180°)和极低的水附着力。原始 SBA-15 的孔均匀性得到了很大的保留,孔体积和孔径与孔内单层烷基硅烷的形成一致。SBA-15 的后合成接枝与 SAMs 不如 CAMs 有效:制备的表面表现出较低的水 CA 和较高的 BET C 常数,从而表明与高度弯曲的介孔表面上的 SAM 支撑相关的受限的可及极性基团(Si-OH)的数量较少。共聚方法产生的无序材料和疏水性表面比任何接枝方法都多。这些材料的表面显示出低水 CA 和高 BET C 常数(约 100-200),从而表明表面覆盖率不均匀,并且存在未改性的二氧化硅。因此得出结论,CAMs 化学是制备具有均匀表面和孔的功能化 OMS 材料的最有效方法。