The e'ects of re-activation on the surface areas and pore volumes are shown in Table 1. The raw material, AC, has relatively high micropore surface area than other samples. But as the treating temperature increased, the ratio of Smi=SBET decreased gradually. In the case of AC800, microand meso surface areas as well as pore volumes were well developed, simultaneously. For the samples of AC900 and AC1000, the rapid declines of surface areas and pore volumes were observed, especially, in the micropore part. It can be thought that the pore volumes of the activated carbons increase with activation temperatures up to about 800◦C. This indicates that the pores enlarge up to this temperature. Above 800◦C, the excess enlargement causes the combination of pores, resulting in the increase of mesopores and the decrease of micropore volume and the surface area as well. The other reason is the graphitization of samples over 900◦C. In Fig. 6, the evidence of graphitization can be seen in the XRD peak shown around the 2 of 26◦. The inAuences of activation temperature on the pore volume of activated carbons are summarized in Fig. 2. This shows that thepreparedactivatedcarbonshavevariousporositieswhich were intended at the start of the present study.
The e'ects of re-activation on the surface areas and pore volumes are shown in Table 1. The raw material, AC, has relatively high micropore surface area than other samples. But as the treating temperature increased, the ratio of Smi=SBET decreased gradually. In the case of AC800, microand meso surface areas as well as pore volumes were well developed, simultaneously. For the samples of AC900 and AC1000, the rapid declines of surface areas and pore volumes were observed, especially, in the micropore part. It can be thought that the pore volumes of the activated carbons increase with activation temperatures up to about 800◦C. This indicates that the pores enlarge up to this temperature. Above 800◦C, the excess enlargement causes the combination of pores, resulting in the increase of mesopores and the decrease of micropore volume and the surface area as well. The other reason is the graphitization of samples over 900◦C. In Fig. 6, the evidence of graphitization can be seen in the XRD peak shown around the 2 of 26◦. The inAuences of activation temperature on the pore volume of activated carbons are summarized in Fig. 2. This shows that thepreparedactivatedcarbonshavevariousporositieswhich were intended at the start of the present study.
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