• Journal of the Korean Ceramic Society
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• v.44 no.6 s.301
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• pp.325-330
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• 2007

High porous AlO(OH) gel is used in precursor of ceramic material, coating material and porous catalyst. For use of these, not only physiochemical control for particle morphology, pore characteristic and peptization but also studies of synthetic method for preparation of high porous AlO(OH) gel were required. In this study, high porous AlO(OH) gel was prepared through the aging and filtration process of aluminum hydroxides gel precipitated by the hydrolysis reaction of $Na_2CO_3$ solution and $Al_2(SO_4)_3$ and $Na_2SO_4$ mixed solution. In this process, optimum synthetic condition of AlO(OH) gel having excellent pore volume as studying the effect of hydrolysis pH on gel precipitates has been studied. Hydrolysis pH brought about numerous changes on crystal morphology, surface area, pore volume and pore size. Physiochemical properties of gel were investigated as using XRD, TEM, TG/DTA, FT-IR and $N_2$ BET method.

• Applied Chemistry for Engineering
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• v.16 no.3
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• pp.391-396
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• 2005

This study was conducted to neutralize acid mine drainage (AMD) of Soo and Hambaek mines, located in Kangwon-Do Korea, using $Ca(OH)_2$. When 0.295 g $Ca(OH)_2/L$(AMD) was added to the drainage in a neutralization reactor, pH of liquid in the reactor and the effluent were maintained at 9.5 and 8.4, respectively. The pH met the required effluent standard. With 10~50% of feedback of effulent sludge to the reactor, the pH of neutralized fluid in the reactor remained nearly constant, but $SO{_4}^{-2}$ concentration in the effluent increased adversely compared to the non-return sludge case. With 30% of sludge feedback, it was possible to decrease suspended solids (SS) concentration in the effluent without a problem in Fe concentration. When 100 mL of 0.1 M $BaCl_2$ was added to 1 L of AMD treated with $Ca(OH)_2$, removal efficiency of $SO{_4}^{-2}$ increased to over 90%. Aanalyses of pH, Fe, and $SO{_4}^{-2}$ showed that the optimal results were obtained when pH of neutralizatio reactor and sludge return ratio were maintained at 9.5 and 30%. This can result in possible cost reduction of 31.4% for maintenance and 29.8% for facility construction by alternating $Ca(OH)_2$ to NaOH.

• Analytical Science and Technology
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• v.19 no.4
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• pp.309-315
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• 2006

Two piperazine-templated metal sulfate complexes, $(C_4N_2H_{12})[Ni(H_2O)_6](SO_4)_2$, I and ($C_4N_2H_{12}$) $[Co(H_2O)_6](SO_4)_2$, II, have been synthesized by hydro/solvothermal reactions and their crystal structures analyzed by single crystal X-ray diffraction methods. Complex I crystallizes in the monoclinic system, $P2_1/n$ space group, a=12.920(3), b=10.616(2), $c=13.303(2){\AA}$, ${\beta}=114.09(1)^{\circ}$, Z=4, $R_1=0.030$ for 3683 reflections; II: monoclinic $P2_1/n$, a=12.906(3), b=10.711(2), $c=13.303(2){\AA}$, ${\beta}=114.10(2)^{\circ}$, Z=4, $R_1=0.032$ for 4010 reflections. The crystal structures of the piperazine-templated metal(II) sulfates demonstrate zero-dimensional compound constituted by diprotonated piperazine cations, metal(II) cations and sulfate anions. The structures of complex I and II are substantially isostructural to that of the previously reported our piperazine-templated copper(II) sulfate complex $(C_4N_2H_{12})[Cu(H_2O)_6](SO_4)_2$. The central metal(II) atoms are coordinated by six water molecules in the octahedral geometry. The crystal structures are stabilized by three-dimensional networks of the $O_{water}-H{\cdots}O_{sulfate}$ and $N_{pip}-H{\cdots}O_{sulfate}$ hydrogen bonds between the water molecules and sulfate anions and protonated piperazine cations. Based on the results of thermal analysis, the thermal decomposition reactions of the complex I was analyzed to have three distinctive stages whereas the complex II proceed through several stages.

• Economic and Environmental Geology
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• v.50 no.1
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• pp.27-34
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• 2017

Mineral carbonation for the storage of carbon dioxide is a CCS option that provides an alternative for the more widely advocated method of geological storage in underground formation. Carbonation of magnesium- or calcium-based minerals, especially the carbonation of waste materials and industrial by-products is expanding, even though total amounts of the industrial waste are too small to substantially reduce the $CO_2$ emissions. The mineral carbonation was performed with steelmaking reduction slag as starting material. The steelmaking reduction slag dissolution experiments were conducted in the $H_2SO_4$ and $NH_4NO_3$ solution with concentration range of 0.3 to 1 M at $100^{\circ}C$ and $150^{\circ}C$. The hydrothermal treatment was performed to the starting material via a modified direct aqueous carbonation process at the same leaching temperature. The initial pH of the solution was adjusted to 12 and $CO_2$ partial pressure was 1MPa for the carbonation. The carbonation rate after extracting $Ca^^{2+}$ under $NH_4NO_3$ was higher than that under $H_2SO_4$ and the carbonation rates in 1M $NH_4NO_3$ solution at $150^{\circ}C$ was dramatically enhanced about 93%. In this condition well-faceted rhombohedral calcite, and rod or flower-shaped aragonite were appeared together in products. As the concentration of $H_2SO_4$ increased, the formation of gypsum was predominant and the carbonation rate decreased sharply. Therefore it is considered that the selection of the leaching solution which does not affect the starting material is important in the carbonation reaction.

• Journal of the Korean Chemical Society
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• v.9 no.1
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• pp.16-22
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• 1965

The time-lag-effect of alkali salts on the gelation of sodium alginate-$CaSO_4{\cdot}$1/2 $H_2O$ is compared with Miyake's data, and then the formation rate of the elastics measured by the continuous method (an improved Schwedoff's method) and the change of rigidity with metallic oxides are studied as follows: (1) The gelation processes of sodium alginate and $CaSO_4{\cdot}$1/2 $H_2O$-aqueous sol are studied by measuring, continuously the increases of tensions ofsamples. (2) The time-lag-effect of $Na_3PO_4$ on the formation rate of the elastic gel is larger than that of $Na_2CO_3$, but the difference between the effects of the two alkali salts on the rate is found not so greater than predicted in Miyake's data. (3) Any regularities of the effect on the rate by metallic oxides are not observed. The increasing effects of the rates of $SiO_2$ and MgO are relatively large, and that of ZnO is relatively small. However, $Al_2O_3$, $Sb_2O_3$ and $TiO_2$show some decreasing effects. As a result it is noted that the regularities do not depend on the effect of oxide species and their amounts. (4) It is not found proportionality between the rigidity and the gelation rate. However, the increasing effect of the rigidity with the addition of metallic oxides can be observed. The rigidity increasing rate of MgO is the largest of them.

• Korean Journal of Environmental Agriculture
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• v.10 no.1
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• pp.59-66
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• 1991

This study was carried out to investigate the chemical characteristics of the rain water in rural, urban and industrial areas which are located in Kyongbuk province, namely. Songju, Kumi, Kimchon, Yongdok and Teagu. The experiments were sampled the rain by amount of rain water from July to August in 1989, and analyzed the pH. EC, $SO_4\;^{2-}$, $NO_3^-$ and $Cl^-$ contents in the rain water. The results are summarized as follows : 1. The acid rain showed at the begining rain water of all surveyed sites, but there were difference by sites, and particulary severe in Kumi. 2. The content of $SO_4\;^{2-}$ in rain water was high in urban and industrial area, such as Teagu, Kumi and Kimchon. 3. According to the increasing rain water amount, the pH in rain water was high, and the contents of other components were low. This phenomenon remarkably presented at higher concentration of components and earlier rain water. 4. The electric conductivity was high significantly positive correlation with contents of $SO_4\;^{2-}$, $NO_3\;^-$ and $Cl^-$ in rain water, and pH was high significantly negative correlation with contents of $SO_4^{2-}$ and $NO_3\;^-$ in rain water, respectively.

• Korean Journal of Environmental Agriculture
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• v.14 no.1
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• pp.45-54
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• 1995

esters of the acid analytes were synthesized using $H_2SO_4$ as the catalyst. Efficiency of derivatization and instrumental molecular-response were compared with herbicides methylated with $BF_3-methanol$(14% W/V), $H_2SO_4-methanol$(33% V/V), and diazomethane. The molecular integrity of TFE-2,4-D, TFE-dicamba, and TFE-mecoprop, in the mixture, was confirmed by the GC/MSD method. The TFE-Esterification efficiency was maximized by adjusting the volume of $H_2SO_4$ the reaction time, and temperature. Optimal efficiency for the herbicide mixture was obtained by adding 1 ml of $H_2SO_4$ and 1 ml of TFE to the dried sample and allowing the reaction to proceed at $22^{\circ}C$ for 8 hr or using 0.5 ml $H_2SO_4$ and 1 ml of TFE at $60^{\circ}C$. For 120 min increasing the temperature and decreasing the reaction time were required for maximum esterification efficiency. The sensitivity of the GC/ECD to the TFE esters was about $2{\sim}20$ times greater than that to the methyl ester derivatives. The herbicides were extracted and esterified to TFE derivatives simultaneously from soil leachates previously spiked with the analytes. Herbicide recovery, peak resolution, and detector sensitivity were excellent without using column cleanup procedures.

• Korean Journal of Soil Science and Fertilizer
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• v.40 no.2
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• pp.151-155
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• 2007

The issue of acid precipitation and related environmental problems in East Asia have been emerging. To evaluate the acidity and chemical characteristics of rainwater in Korea, its chemical properties during crop cultivation season from April to October were investigated at Suwon, Korea. Also, to estimate the contribution of ions on its acidity, ion composition characteristics and neutralization effects by cation ions were determined. Ion balance and electrical conductivity balance between the measured and estimated values showed high correlation. Rainwater had distributed highly in the range of pH 4.5~5.6. The pH of rainwater was relatively high at June as compared with other monitoring periods. $Na^+$ was the main cation followed by $NH_4{^+}$, $Ca^{2+}$, $H^+$ > $K^+$ > $Mg^{2+}$. Among these, $Na^+$, $NH_4{^+}$, $Ca^{2+}$ and $H^+$ covered over 93% of total cations. About 86% of anion in rainwater was composed of $SO{_4}^{2-}$ and $NO_3{^-}$. In rainwater samples, $NH_4{^+}$ and $Ca^{2+}$ contributed greatly to neutralization of the rain acidity. Also, 88% of soluble sulfate in rainwater was nss-$SO{_4}^{2-}$(non-sea salt sulfate).

• Journal of environmental and Sanitary engineering
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• v.14 no.3
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• pp.99-106
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• 1999

This research was carried out to investigate chemical pretreatment using lime and limestone in treating abandoned mine drainage with anaerobic treatment. If treating lime with abandoned mine drainage, after 2day, pH was increased to 5.6, and $SO_4^{2-}$, Fe, Al, Pb and Mn were removed 5.7%, 63%, 57, 45% and 28%, respectively. It was estimated that lime dosage was 2,000mg/L for increasing to pH 7. If treating limestone with abandoned mine drainage, after 2day, pH was increased to 3.67, and $SO_4^{2-}$, Fe, Al, Pb and Mn were removed 4.7%, 26%, 22% 18% and 8%, respectively. It could be showed that limestone did slowly react with temperature increasing. If treating anaerobic limestone packing column with abandoned mine drainage, for experimental period, average pH was 4.51, and average $SO_4^{2-}$, Fe, Al, Pb and Mn were removed 4.5%, 15.3%, 20.1%, 23.7% and 5.87%, respectively. So, it would not be suitable for abandoned mine drainage. But if utilizing limestone as pretreatment process for treating abandoned mine drainage with SRB, because it did initally neutralize abandoned mine drainage, it could forward to stabilize system.

• KSBB Journal
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• v.8 no.4
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• pp.409-414
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• 1993

This study was designed to reveal the conditions for $\beta$-glucosidase production from Aspergillus niger. The maximal enzyme production was obtained when the fungus was cultured at $30^{\circ}C$ for 5~6 days in the optimal medium containing 0.8% CMC, 0.5% beef extract, 0.3% Ca(NO3)2, 0.03% K2HPO4, 0.03% FeSO4, 0.05% Li2SO4, 0.2% tween 80, trace solution 1.0ml and initial pH 4.0, and then final enzyme activity under above conditions was 8.5-9.8 unit/ml culture filtrate.