Delpeux Sandrine, Szostak Katarzyna, Frackowiak Elzbieta, Bonnamy Sylvie, Béguin François
CRMD, CNRS-University, 1B, rue de la Férollerie, 45071 Orléans, France.
J Nanosci Nanotechnol. 2002 Oct;2(5):481-4. doi: 10.1166/153348802760394034.
For the first time, multiwalled carbon nanotubes (MWNTs) could be formed selectively in a high yield, free of any disordered carbon by-product, from the catalytic decomposition of acetylene at 600 degrees C on a CoxMg(1-x)O solid solution. Starting from 1 g of catalytic substrate, 4 g of pure MWNTs were obtained after its dissolution in boiling concentrated HCl, without any additional purification in strongly oxidizing medium, as is required for other methods of nanotube production. In situ reduction of CoO by dihydrogen liberated from acetylene decomposition allows highly divided metal particles to be continuously produced as synthesis proceeds. This is undoubtedly the reason for the good performance of the catalyst and for the ability to produce nanotubes in a narrow diameter range, namely from 10 to 15 nm. With the use of acetylene instead of methane, the synthesis proceeds at low temperature, which prevents the growth of carbon shells, in which the metal particles are generally embedded, decreasing their activity. Because of the very low specific surface area of the catalyst support, the amount of disordered carbon by-product formed is negligible.
首次能够在600摄氏度下,通过乙炔在CoxMg(1-x)O固溶体上的催化分解,以高收率选择性地形成多壁碳纳米管(MWNTs),且无任何无序碳副产物。从1克催化底物开始,将其溶解在沸腾的浓盐酸中后,无需像其他纳米管生产方法那样在强氧化介质中进行任何额外纯化,即可获得4克纯MWNTs。乙炔分解释放出的氢气对CoO进行原位还原,使得随着合成的进行能够持续产生高度分散的金属颗粒。这无疑是催化剂性能良好以及能够在10至15纳米的窄直径范围内生产纳米管的原因。使用乙炔而非甲烷时,合成在低温下进行,这可防止通常包裹着金属颗粒并降低其活性的碳壳生长。由于催化剂载体的比表面积非常低,所形成的无序碳副产物的量可忽略不计。