Pore structure of C/C （Carbon-Carbon） composite after several stages of pitch impregnation under the high pressure and heat treatment was investigated by means of low temperature nitrogen adsorption and the standard...Pore structure of C/C （Carbon-Carbon） composite after several stages of pitch impregnation under the high pressure and heat treatment was investigated by means of low temperature nitrogen adsorption and the standard contact porosimetry. Total pore volume, pore size distribution and specific surface area were calculated for samples of composite after several successive stages of treatment. The radius of pores presented in the material changes from 1 nm to 90 tam. Total pore volume and specific surface area both decrease after successive stages of pitch impregnation under the pressure, whereas heat treatment up to 1,750 ℃ and 2,000 ℃ leads to creation of some porous space and pore volume expansion. The bulk porosity of C/C composite comes down from 33.7% to 13.7% after the serial stages of treatment and the specific surface area is reduced by half compared to the initial material.展开更多
In this study, bamboo scaffolding was used to produce activated carbon by carbonization at 600 ℃ and 900 ℃with the purge of nitrogen. The 600 ℃ char was then further modified chemically by acids and alkalis by refl...In this study, bamboo scaffolding was used to produce activated carbon by carbonization at 600 ℃ and 900 ℃with the purge of nitrogen. The 600 ℃ char was then further modified chemically by acids and alkalis by reflux for 6 hours. The produced chars were then characterized by nitrogen adsorption isotherm, He pyncometry, pH, elemental analysis and Boehm titration. For most of the chemically modified carbons, the micropore surface areas and volumes have increased compared with the 600 ~C char, while the mesopore surface areas and volumes slightly decreased, which may have been due to the dissolving of some of the permeated inorganic matter and oxidizing deposited carbon that blocks the pore openings. For the acidic modified carbons, larger amounts of acidic groups were present in the carbons after being activated by phosphoric acid, phosphoric acid furth, er treated with 2 mol-L-1nitric-acid, and calcium hydroxide. Although carbon treated with 2 mol.L-1 and 5 mol·L-1 nitric acid also produced high acidity, the surface areas and pore volumes were relatively low, due to the destruction of pores by nitric acid oxidation. The reduction of porosity may impair the adsorption capacity.展开更多
文摘Pore structure of C/C （Carbon-Carbon） composite after several stages of pitch impregnation under the high pressure and heat treatment was investigated by means of low temperature nitrogen adsorption and the standard contact porosimetry. Total pore volume, pore size distribution and specific surface area were calculated for samples of composite after several successive stages of treatment. The radius of pores presented in the material changes from 1 nm to 90 tam. Total pore volume and specific surface area both decrease after successive stages of pitch impregnation under the pressure, whereas heat treatment up to 1,750 ℃ and 2,000 ℃ leads to creation of some porous space and pore volume expansion. The bulk porosity of C/C composite comes down from 33.7% to 13.7% after the serial stages of treatment and the specific surface area is reduced by half compared to the initial material.
基金the support of Hong Kong University of Science and Technology through the Undergraduate Research Opportunity Program
文摘In this study, bamboo scaffolding was used to produce activated carbon by carbonization at 600 ℃ and 900 ℃with the purge of nitrogen. The 600 ℃ char was then further modified chemically by acids and alkalis by reflux for 6 hours. The produced chars were then characterized by nitrogen adsorption isotherm, He pyncometry, pH, elemental analysis and Boehm titration. For most of the chemically modified carbons, the micropore surface areas and volumes have increased compared with the 600 ~C char, while the mesopore surface areas and volumes slightly decreased, which may have been due to the dissolving of some of the permeated inorganic matter and oxidizing deposited carbon that blocks the pore openings. For the acidic modified carbons, larger amounts of acidic groups were present in the carbons after being activated by phosphoric acid, phosphoric acid furth, er treated with 2 mol-L-1nitric-acid, and calcium hydroxide. Although carbon treated with 2 mol.L-1 and 5 mol·L-1 nitric acid also produced high acidity, the surface areas and pore volumes were relatively low, due to the destruction of pores by nitric acid oxidation. The reduction of porosity may impair the adsorption capacity.
