滑动流气透法测量比表面的研究——Blatne仪器法

本文由粉末床层的滑动流一般公式推导出 Blaine 仪测量计算比表面 S_V 的公式,对一些粉末进行了测量研究,使简便的 Blaine 仪扩大应用到细粉末范围。结果表明,粘滞流公式不适用于亚微米粉末,用粘滞流公式计算的 S_K 对于 S_V 的误差随粉末粒度和床层孔度的减小而增大。本文还讨论了测量计算的 S_V 随孔度变化的复杂原因。

The performance of nano multicomponent cocatalyst in the improvement of catalytic sensor of methane

Based on the deficiency of catalytic elements in methane sensors such as sintering,activity decrease and surface area reduction at high temperature, three differentnano vectors Ce-Zr-Al_2O_3, Ce-Al_2O_3, and Zr-Al_2O_3 were prepared via sol-gel technique inthe experiment.BET surface area, catalytic activity and thermal stability were tested andcompared.It is found from the experiment that the Ce-doped Al_2O_3 vector possesseshigher catalytic activity than pure Al_2O_3 vector.Zr-doped Al_2O_3 vector can enhance thethermal stability of methane sensors.Ce-Zr-Al solid solution can be obtained by the presenceof Ce and Zr doped with Al_2O_3.The reaction activity and thermal stability of catalyticsensors were improved because of the unique synergy effect from Ce-Zr-O.Among themixed cocatalysts, Ce-Zr-O was reported to be an excellent cocatalyst material.The performanceof methane sensors can be improved significantly via the modification ofCe-Zr-Al_2O_3 vector.

Change in the Pore Structure of Carbon-Carbon Composites during Successive Stages of High-Pressure Impregnation and Heat Treatment

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.

Characteristics of Chemical Modified Activated Carbons from Bamboo Scaffolding

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.

What are the practical limits for the specific surface area and capacitance of bulk sp^2 carbon materials?

The possible practical limits for the specific surface area and capacitance performance of bulk sp^2 carbon materials were investigated experimentally and theoretically using a variety of carbon materials. We find the limit for the specific surface area to be 3500–3700 m^2 g^(-1), and based on this, the corresponding best capacitance was predicted for various electrolyte systems. A model using an effective ionic diameter for the electrolyte ions was proposed and used to calculate the theoretical capacitance. A linear dependence of experimental capacitance versus effective specific surface area of various sp^2 carbon materials was obtained for all studied ionic liquid, organic and aqueous electrolyte systems. Furthermore, excellent agreement between the theoretical and experimental capacitance was observed for all the tested sp^2 carbon materials in these electrolyte systems, indicating that this model can be applied widely in the evaluation of various carbon materials for supercapacitors.