• Restorative Dentistry and Endodontics
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• v.40 no.4
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• pp.290-298
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• 2015

Objectives: Sodium hypochlorite (NaOCl) is an excellent bactericidal agent, but it is detrimental to stem cell survival, whereas intracanal medicaments such as calcium hydroxide ($Ca[OH]_2$) promote the survival and proliferation of stem cells. This study evaluated the effect of sequential NaOCl and $Ca(OH)_2$ application on the attachment and differentiation of dental pulp stem cells (DPSCs). Materials and Methods: DPSCs were obtained from human third molars. All dentin specimens were treated with 5.25% NaOCl for 30 min. DPSCs were seeded on the dentin specimens and processed with additional 1 mg/mL $Ca(OH)_2$, 17% ethylenediaminetetraacetic acid (EDTA) treatment, file instrumentation, or a combination of these methods. After 7 day of culture, we examined DPSC morphology using scanning electron microscopy and determined the cell survival rate with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. We measured cell adhesion gene expression levels after 4 day of culture and odontogenic differentiation gene expression levels after 4 wk using quantitative real-time polymerase chain reaction. Results: DPSCs did not attach to the dentin in the NaOCl-treated group. The gene expression levels of fibronectin-1 and secreted phosphoprotein-1 gene in both the $Ca(OH)_2$- and the EDTA-treated groups were significantly higher than those in the other groups. All $Ca(OH)_2$-treated groups showed higher expression levels of dentin matrix protein-1 than that of the control. The dentin sialophosphoprotein level was significantly higher in the groups treated with both $Ca(OH)_2$ and EDTA. Conclusions: The application of $Ca(OH)_2$ and additional treatment such as EDTA or instrumentation promoted the attachment and differentiation of DPSCs after NaOCl treatment.

• Journal of the Korean institute of surface engineering
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• v.19 no.4
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• pp.133-139
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• 1986

The effects of alternating voltage, $Cl^-$ ion and pH on the corrosion of Zn and Zn-Fe alloys have been investigated by using electrochemical techniques in $Ca(OH)_2$ solutions. The passive film $Zn(OH)_2$ was initially formed on the Zn surface and gradually transformed to $Ca(Zn(OH)_3)_2{\cdot}2H_2O$, which was identified with the X-ray diffraction method, SEM micrograph and EPMA. The passivity current increased with increasing alternating voltage and decrease AC frequency. ${\xi}$ phase in Zn-Fe alloys reduced the effects of AC. The effect of $Cl^-$ ion on the passivity current of Zn was similar to the AC effect, resulting in pits on Zn. It was also found that the passive region of Zn decreased rapidly below pH 10.3 of the solution.

• Korean Chemical Engineering Research
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• v.47 no.6
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• pp.727-733
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• 2009

Effects of $Ca(OH)_2$ concentration(0.16~0.64 wt%), total volumetric flow rate(3~6 L/min) and $CO_2$ volume fraction(0.3~0.6) on morphology of the precipitated $CaCO_3$ and the mean particle size of the precipitated $CaCO_3$ were investigated in the slurry bubble column reactor. Experiments were carried out in acrylic reactor($0.11m-ID{\times}1.0m-high$) with a internal tube($0.04m-ID{\times}1.0m-high$). The calibration curve on the mass ratio of $CaCO_3$ to $Ca(OH)_2$ was obtained by FT-IR for the conversion of $Ca(OH)_2$ with the reaction time. The reaction rate of $Ca(OH)_2$ increased with increasing the volumetric flow rate of $CO_2$. From SEM images, the crystal size of $CaCO_3$ increased with increasing the reaction rate in the saturated concentration of $Ca(OH)_2$ (0.16 wt%). In addition, the crystal size of precipitated $CaCO_3$ decreased with increasing the concentration of $Ca(OH)_2$, but the mean particle size of precipitated $CaCO_3$ increased with increasing the concentration of $Ca(OH)_2$.

• Solar Energy
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• v.17 no.1
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• pp.67-77
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• 1997

To develop chemical heat pump of higher energy density and efficiency heat-release characteristics accompanied by exothermic hydration reaction in packed bed, $Ca(OH)_2/CaO$ reactor, are examined in a lab-scale unit. We have studied the enhancement effect of inserted fins in cylindical packed bed reactor. The results obtained by numerical analysis about profiles of temperature, completion time of reaction and exothermic heat amount released from the reactor read the insertion of fins in reactor can reduce the reaction completion time by half and the rate of thermochemical reaction depends on the temperature and concentration, and it is also governed by the boundary conditions and the rate of heat transfer in the particle packed bed.

• Journal of the Korean Ceramic Society
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• v.29 no.1
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• pp.74-82
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• 1992

Ultra-fine calcium phosphate powders were synthesized by the reaction of Ca(OH)2 suspension with various phosphoric aqueous solutions such as (NH4)2HPO4, H4P2O7 and H3PO4, and the characterization of powders was examined for each synthetic condition. When (NH4)2HPO4 and H3PO4 were used, hydroxyapatite powders with poor crystallinity were obtained. In the case of H4P2O7, amorphous calcium phosphate was obtained up to 0.3 mol/ι Ca(OH)2 suspension, but above the concentration, poor crystalline hydroxyapatite was produced. Crystalline phases of powders heat-treated at 80$0^{\circ}C$ were hydroxyapatite, $\beta$-tricalcium phosphate and $\beta$-tricalcium phosphate for the case of (NH4)2HPO4, H4P2O7 and H3PO4, respectively. SEM observation revealed that the shapes of synthesized powders were vigorously agglomerated spherical with the size below 100 nm, but TEM observation revealed that primary shapes of particles were rod for (NH4)2HPO4 and H3PO4 and were sphere for H4P2O7. There was no dependence of the concentration of Ca(OH)2 suspension. In the case that reaction temperature and pH of the suspension were raised, the inclination to the hydroxyapatite were remarkable. The amorphous calcium phosphate synthesized in this experiment contained water about 20% , and was crystallized to $\beta$-tricalcium phosphate at 69$0^{\circ}C$.

• Journal of Korean Society of Environmental Engineers
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• v.35 no.5
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• pp.340-349
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• 2013

The present paper investigates the availability of seawater as the absorbents to capture carbon dioxide ($CO_2$) emitted from the coal fired power plant (CFPP). For the purpose of the study, readily obtainable alkali materials in CFPP such as coal fly ash (FA), NaOH and $Ca(OH)_2$ are added to seawater to prepare the absorbents and their $CO_2$ capture performances are discussed. FA can be effectively used the additives to increase $CO_2$ capture capacity of seawater to a some extent. This is ascribed that some alkali components in FA are leached into seawater and they contribute to $CO_2$ capture in the solution. However, their leaching amount and rate are restricted by the various ions in seawater. The performance of NaOH added seawater is even lower than that of NaOH added water because $OH^-$ is substantially consumed on $Ma(OH)_2$ production prior to carbonation. $CO_2$ absorption capacity of $Ca(OH)_2$ added seawater is slightly larger than that of $Ca(OH)_2$ added water. This is because that $Ca^{2+}$ which originally present in raw seawater can participate in carbonation reaction.

• Journal of Korean Society of Water and Wastewater
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• v.11 no.1
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• pp.53-63
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• 1997

The corrosion problems in water distribution system are reduced by decreasing the agressivity of drinking water which is evaluated by marble test and saturation indices(LSI or CCPP etc.). Marble test is a reliable method to determine the actual saturation condition of treated water. This study was done to determined the aggressivity of tap water and the effectiveness of $Ca(OH)_2$ and NaOH dosage for corrosion control. The drinking water in Seoul were evaluated by marble test and Langelier Index(LSI) and Calcium Carbonate Precipitation Potential(CCPP). The results indicated that the drinking water in Seoul were undersaturated as Calcium Carbonate($CaCO_3$). The LSI and CCPP of the water treated with $Ca(OH)_2$ were higher than that of water treated with NaOH. Therefore, to increase the Alkalinity and Calcium Hardness for corrosion control in water distribution system, $Ca(OH)_2$ is more effective than NaOH.

• Korean Journal of Environmental Agriculture
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• v.29 no.2
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• pp.102-108
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• 2010

The effects of foliar spray of calcium hydroxide ($Ca(OH)_2$) during fruit growth period was investigated by changes of the shoot growth and fruit quality in 'Daewol' peach (Prunus persica). Since foliar spray of $Ca(OH)_2$ 1, 2, 5, and 10 $g{\cdot}L^{-1}$ at 7 day-intervals after fruit thinning, shoot growth was remarkably decreased compared with control group. An average SPAD value of fifth leaf from proximal part of the shoot was higher as 42.1 specific color difference sensor value (SCDSV) of $Ca(OH)_2$ foliar spraying treatments than 40.9 SCDSV of control group. Photosynthesis rates were also significantly increased by treating $Ca(OH)_2$ of higher concentration. Among fruit characteristics affecting quality, fruit weight was increased depending on concentration of $Ca(OH)_2$ treatment. The soluble solids content was lowest in control group (8.78 $^{\circ}Brix$) compare with higher concentrations of $Ca(OH)_2$ foliar spraying treatment in each 9.17, 9.22, 9.71, 10.58 $^{\circ}Brix$. The acidity and anthocyanin contents were no significant differences among treatment, but firmness of pericarp and flesh of fruits was significantly increased by $Ca(OH)_2$ foliar spray treatment. As a results of morphological observation of leaf, thickness of palisade parenchyma was thinner in control group (63.5 ${\mu}m$) than those of each 86.5, 87.5, 93.6, 107.4 ${\mu}m$ in $Ca(OH)_2$ foliar spraying treatment. Higher $Ca(OH)_2$ foliar spray also increased the thickness of cell wall of epidermis and hypodermis in 'Daewol' fruit.

• Journal of the Korean Chemical Society
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• v.39 no.7
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• pp.578-584
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• 1995

An aqueous solution of $Ca(OH)_2$ containing a small amount of dissolved $Sr(OH)_2$ was carbonated with $CO_2$ gas, and the effects of the reaction temperature and $Sr(OH)_2$ on the carbonation were investigated. The higher the reaction temperature and the larger the ratio of $Sr(OH)_2(aq)$ to $Ca(OH)_2(aq)$, which amounts to the larger the ratio of $OH^-$ to $CO_2(aq)$, the better pillar aragonite was formed. $Sr(OH)_2$ played an important role in the formation of pillar aragonite, because it is easily formed itself into rhombic $SrCO_3$ during the initial period of carbonation process and acting as a seed for the pillar aragonite of similar morphology. In addition, due to its substantially higher solubility compared with $Ca(OH)_2$, $OH^-$ concentration in the carbonation mixture and subsequently $CO_3^{2-}$ necessary for the crystal growth are increased.

• Corrosion Science and Technology
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• v.15 no.6
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• pp.303-310
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• 2016

The tap water used in Seoul was found to be corrosive. Its corrosivity was effectively reduced by that the additions of alkali agent such as NaOH, $Ca(OH)_2$ and corrosion inhibitor such as $H_3PO_4$. For the corrosion test, carbon steel pipe 50 m long was exposed to the drinking water produced by a pilot plant at $36.5^{\circ}C$, similar to the existing process where it takes about 20 minutes to reduce the initial chlorine content of 0.5 mg/L to 0.05 mg/L. $CO_2$ and $Ca(OH)_2$ was added not only to control the Langelier index (LI) above -1.0 and but also, to increase the duration time of residual chlorine by about 6 times. The persistence effect of residual chlorine was in the order of $H_3PO_4$ > $Ca(OH)_2$ > NaOH. Measurements of weight loss showed that corrosion inhibition was effective in order of $Ca(OH)_2$ > $H_3PO_4$ > NaOH > no addition, where the concentrations of $Ca(OH)_2$ and phosphate were 5 ~ 10 mg/L (as $Ca^{2+}$) and 1 mg/L (as $PO{_4}^{3-}$), respectively.