The chemical activation of a carbon precursor with KOH generally results in an activated carbon (AC) with a high specific surface area. However, this process generates a large volume of wastewater that includes dissolved alkali metals, existing mainly as K2CO3. Thus, wastewaters with a high concentration of dissolved K2CO3 can potentially be used in place of KOH as a chemical agent. In the present study, to reduce the thermal stability of K2CO3, which decomposes at temperatures greater than 891 °C, K2CO3 was chemically impregnated into carbon precursors prior to activation of the precursors. The thermochemical properties and activation efficiency of the carbon precursors treated with K2CO3 were compared with those of carbon precursors treated with KOH. Analysis by XPS indicated that C–O–K complexes formed on the surface of the carbon precursors; in addition, their peak intensities were approximately the same irrespective of the chemical agent used. However, the specific surface area of the K2CO3-impregnated AC was 2162 m2/g, which was ~70% of that of the KOH-impregnated AC (3047 m2/g) prepared using the same K/C molar ratio of 0.5. XRD results confirmed that both K2CO3 and KOH transformed into KHCO3 and K4H2(CO3)3·1.5H2O during the impregnation. The peak intensities of these compounds in the XRD pattern of the K2CO3-impregnated carbon precursors were two times greater than those in the pattern of the KOH-impregnated carbon precursors. These compounds eventually transformed into K2CO3, which hardly participated as a chemical agent at the temperature used in the present study (850 °C). Therefore, recrystallisation of K2CO3, even during the impregnation, appeared to adversely affect the degree of activation. Nevertheless, the specific surface area of the K2CO3-activated AC was still ~1.6 times greater than that of the untreated carbon precursor (1378 m2/g), suggesting that the use of wastewater as a chemical agent is feasible for resource recycling.

Mass flow meters (MFMs) are widely used to secure reliable flow rates based on the mass value of the gas being measured. However, chemical reactions produce various kinds of gases, and their composition also changes in real time. Thus, there may be a large deviation in the gas flow if the gases’ composition and its mixing ratio are not known. In this study, we derived a gas flow rate measurement method using a chemically stable chemical specie and verified the precision of the proposed method through comparative analysis with an MFM. The flow rate by this method showed reliable results in both single and mixed gases. Notably, the results were within ±2.74% of the injected flowrate values in the gas mixtures. This method is expected to be able to fundamentally overcome the limitations of the mechanical flowmeter because it is not affected by changes in gas composition or mixing ratio during the reaction.