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Introduction to Nanotechnology

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10.2. CATALYSIS 269<br />

are also other materials such as silicas and aluminas which can be prepared so that<br />

they have a porous structure of a more or less random type; that is, they serve as<br />

sponges on a mesoscopic or micrometer scale. It is quite common for these materials<br />

<strong>to</strong> have pores with diameters in the nanometer range. Pore surface areas are<br />

sometimes determined by the Brunauer-Emmett-Teller (BET) adsorption isotherm<br />

method in which measurements are made of the uptake of a gas such as nitrogen<br />

(N2) by the pores.<br />

Most commercial heterogeneous catalysts have a very porous structure, with<br />

surface areas of several hundred square meters per gram. Ordinarily an hetero-<br />

geneous catalyst consists of a high-surface-area material that serves as a catalyst<br />

support or substrate, and the surface linings of its pores contain a dispersed active<br />

component, such as acid sites or platinum a<strong>to</strong>ms, which bring about or accelerate the<br />

catalytic reaction. Examples of substrates are the oxides silica (Si02), gamma-<br />

alumina (y-A1203), titania (Ti02 in its tetragonal anatase form), and zirconia (ZrOz).<br />

Mixed oxides are also in common use, such as high-surface-area silica-alumina.<br />

A porous material ordinarily has a range of pore sizes, and this is illustrated by the<br />

upper right spectrum in Fig. 10.8 for the organosilicate molecular sieve MCM-41,<br />

which has a mean pore diameter of 3.94 nm (39.4 A). The introduction of relatively<br />

large trimethylsilyl groups (CH3)3Si <strong>to</strong> replace pro<strong>to</strong>ns of silanols SiH30H in the<br />

pores occludes the pore volume, and shifts the distribution of pores <strong>to</strong> a smaller<br />

range of sizes, as shown in the lower left spectrum of the figure. The detection of the<br />

nuclear magnetic resonance (NMR) signal from the 29Si iso<strong>to</strong>pe of the trimethylsilyl<br />

groups in these molecular sieves, with its +12ppm chemical shiR shown in<br />

Fig. 10.9, confirmed its presence in the pores after the trimethylsilation treatment.<br />

-1<br />

7.<br />

Parent MCM-41<br />

[ '" Silylated MCM-41<br />

1.2 30.4 a<br />

0.4 F- \<br />

0 20 25 30 35 40 45 !<br />

Pore Diameter, A<br />

Figure 10.8 Distribution of pore diameters in two molecular sieves with mean pore diameters of<br />

3.04 and 3.94 nm, determined by the physisorption of argon gas. [From J. S. Beck, J. C. Vartuli,<br />

W. J. Roth, M. E. Leonowicz, C. T. Kresge, K. D. Schmitt, C. T.-W. Chu, D. H. Olson,<br />

E. W. Sheppard, S. B. McCullen, J. B. Higgins, and J. L. Schenkler, J. Am. Chem. SOC. 114,<br />

10834 (1 962).]

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