Geopolymer is an alumina silicate-based ceramic material that has good heat-resistance and fire-resistance; it can be cured at room temperature, and thus its manufacturing process is simple. Geopolymer can be used as a reinforcement or floor finish for high-speed curing applications. In this manuscript, we investigate a high-speed curing geopolymer achieved by adding calcium to augment the curing rate. Metakaolin is used as the main raw material, and aqueous solutions of KOH and K2SiO3 are used as the activators. As a result of optimizing the high bending strength as a target factor for geopolymers with SiO2 / Al2O3 ratio of 4.1 ~ 4.8, the optimum ranges of the active agent are found to be 0.1 ≤ K2O / SiO2 ≤ 0.4 and 10 ≤ H2O / K2O ≤ 32.5, and the optimum range of the curing accelerator is found to be 0.82 Ca (OH)2 / Al2O3 2.87. The maximum flexural strength is found to be 1.35 MPa at Ca (OH)2 / Al2O3 = 2.82, K2O / SiO2 = 0.3, and H2O / K2O = 11.3. The physical and thermal properties are analyzed to validate the applicability of these materials as industrial insulating parts or repairing·finishing materials in construction.

Corrosion inhibitors including calcium hydroxide have been used to prevent corrosion in the pipes for tap water supply. The corrosion index (i.e., Langelier Index) differs by area and water quality. The corrosion indices of the areas studied differed by more than 2.0. The ‘homogenized’ calcium hydroxide was added to the treated water at the K water treatment plant, in order to increase the value of the corrosion index and the concentration of calcium. As the result, the concentration of calcium was increased while the turbidity and pH changed little. The corrosion rate of the tap water with the 'homogenized' calcium hydroxide could be slowed down pretty much. The results suggested that the technology of 'homogenization' of calcium hydroxide can applied to tap water and desalinated water to prevent corrosion in water pipes even in corrosive pipes.

Researches on the elimination of sulfur and nitrogen oxides with catalysts and absorbents reported many problems related with elimination efficiency and complex devices. In this study, decomposition efficiency of harmful gases was investigated. It was found that the efficiency rate can be increased by moving the harmful gases together with SPCP reactor and the catalysis reactor. Calcium hydroxide(Ca(OH)2), CaO, and TiO2 were used as catalysts. Harmful air polluting gases such as SO2 were measured for the analysis of decomposition efficiency, power consumption, and voltage according to changes to the process variables including frequency, concentration, electrode material, thickness of electrode, number of electrode winding, and additives to obtain optimal process conditions and the highest decomposition efficiency. The standard sample was sulfur oxide(SO2). Harmful gases were eliminated by moving them through the plasma generated in the SPCP reactor and the Ca(OH)2 catalysis reactor. The elimination rate and products were analyzed with the gas analyzer (Ecom-AC,Germany), FT-IR(Nicolet, Magna-IR560), and GC-(Shimazu). The results of the experiment conducted to decompose and eliminate the harmful gas SO2with the Ca(OH)2 catalysis reactor and SPCP reactor show 96% decomposition efficiency at the frequency of 10 kHz. The conductivity of the standard gas increased at the frequencies higher than 20 kHz. There was a partial flow of current along the surface. As a result, the decomposition efficiency decreased. The decomposition efficiency of harmful gas SO2 by the Ca(OH)2 catalysis reactor and SPCP reactor was 96.0% under 300 ppm concentration, 10 kHz frequency, and decomposition power of 20 W. It was 4% higher than the application of the SPCP reactor alone. The highest decomposition efficiency, 98.0% was achieved at the concentration of 100 ppm.

With industrial development, energy demands continue to rise. Fossil fuels release more air pollutants to produce the same amount of energy compared with other types of fuel. The harmful exhaust gas exacerbated by the increasing uses of vehicles also makes a contribution to the worsening of air pollution. Thus there is a need for various processing methods and technologies to eliminate harmful gases such as sulfur oxides released into the air. Researches on the elimination of sulfur and nitrogen oxides with catalysts and absorbents reported many problems due to elimination efficiency and complex devices. In an attempt to supplement them, this study set out to increase the decomposition efficiency of harmful gases by moving them through the plasma generated in the SPCP reactor and the catalysis reactor specially designed and manufactured. The study used calcium hydroxide(Ca (OH)2),CaO,andTiO2 as catalysts. Harmful air polluting gases such as SO2 were measured for decomposition efficiency, power consumption, and voltage according to changes to the process variables including frequency, concentration, electrode material, thickness of electrode, number of electrode winding, and additives to obtain optimal process conditions and the highest decomposition efficiency. The standard sample was sulfur oxide(SO2). Harmful gases were eliminated by moving them through the plasma generated in the SPCP reactor and the Ca(OH)2 catalysis reactor. The elimination rate and products were analyzed with the gas analyzer (Ecom-AC,Germany), FT-IR(Nicolet, Magna-IR560), and GC-(Shimazu). The results of the experiment conducted to decompose and eliminate the harmful gas SO2with the Ca(OH)2 catalysis reactor and SPCP reactor show 96 decomposition efficiency at the frequency of 10kHz. The conductivity of the standard gas increased according to frequency at high voltage of 20 kHz or more. There was a partial flow of current along the surface. As a result, the decomposition efficiency decreased. The use of tungsten electrode resulted in the highest decomposition efficiency by the Ca(OH)2 catalysis reactor and SPCP reactor, and it was followed by the copper and aluminum electrode in the order. As for the impacts of thickness of electrode at electric discharge, the thicker the electrode was, the higher decomposition efficiency became. As for the number of electrode winding, the more it was wound, the higher decomposition efficiency became. The decomposition efficiency of harmful gas SO2 by the Ca(OH)2 catalysis reactor and SPCP reactor was 96.0% under the conditions of 300ppm concentration, 10kHz frequency, and decomposition power of 20W. It was higher than 92% when only the SPCP reactor was used. Decomposition efficiency was the highest at 98.0% when the concentration was 100ppm. As for the effects of additives to fit actual exhaust gases, the more methane (CH4) was added, the higher decomposition efficiency became over 99%. The higher the oxygen concentration was, the higher decomposition efficiency became, as well

In this study, the air pollutant removal such as sulfur oxides was studied. A combination of the plasma discharge in the reactor by the reaction surface discharge reactor Calcium hydroxides catalytic reactor and air pollutants, hazardous gas SOx, changes in gas concentration, change in frequency, the thickness of the electrode, kinds of electrodes and the addition of simulated composite catalyst composed of a variety of gases, including decomposition experiments were performed by varying the process parameters. The experimental results showed the removal efficiency of 98% in the decomposition of sulfur oxides removal experiment when Calcium hydroxides catalysts and the tungsten(W) electrodes were used. It was increased 3% more than if you do not have the catalytic. If added to methane gas was added the removal efficiency increased decomposition.

Recently, self-healing concrete has been researched as maintenance and repair of concrete structures are important challenges we face. This paper focused on possibility of ion exchange resin as a novelty material directly and actively controlling harmful ions of concrete, whereas most self-healing concrete researches have been focused on methods to automatically filling and repairing internal crack of concrete. Because equilibrium properties between ion exchange resin and harmful ion is important before design of cement mixing proportion, it was conducted to remove chloride or sulfate in saturated Ca(OH)2 solutions containing NaCl or Na2SO4. The removal performance was analyzed using kinetic equation and isothermal equation. Consequently, the removal properties of anion exchange resin were relatively more dependent on pseudo second reaction equation and Langmuir equation than pseudo first reaction equation and Freundlich equation. And it was concluded that each chloride and sulfate can be removed to the maximum 1068 ppm and 1314 ppm.

Carbonation is one of the most critical deterioration phenomena to concrete structures exposed to high CO2 concentration, sheltered from rain. Lots of researches have been performed on evaluation of carbonation depth and changes in hydrate compositions, however carbonation modeling is limitedly carried out due to complicated carbonic reaction and diffusion coefficient. This study presents a simplified carbonation model considering diffusion coefficient, solubility of Ca(OH)2, porosity reduction, and carbonic reaction rate for low concentration. For verification, accelerated carbonation test with varying temperature and MIP (Mercury Intrusion Porosimetry) test are carried out, and carbonation depths are compared with those from the previous and the proposed model. Field data with low CO2 concentration is compared with those from the proposed model. The proposed model shows very reasonable results like carbonation depth and consuming Ca(OH)2 through reduced diffusion coefficient and porosity compared with the previous model.