• Bulletin of the Korean Chemical Society
• /
• v.22 no.12
• /
• pp.1297-1298
• /
• 2001

• Journal of the Korean Chemical Society
• /
• v.29 no.2
• /
• pp.80-87
• /
• 1985

Radiation damage in a single crystal of ammonium sulfate caused by ${\gamma}$-irradiation at room temperature has given rise to several paramagnetic centers. Electron spin resonance (ESR) spectra of crystal are obtained with the X-band EPR spectrometer at room temperature. An intense and isotropic peak of Gaussian shape at g = 2.0036 is assigned to $SO_3^-$, which shows power saturation effects. Angular dependence of spectra is studied for the rotations about three mutually perpendicular axes a, b and c. The g-values are obtained from the relative distances between isotropic peak of $SO_3^-$ and anisotropic peak of the species. Principal $g^-$values and direction cosines were calculated by diagonalizing the 3${\times}$3 matrix whose elements are the $g^-$values for each species. From the analysis of characteristic principal $g^-$values and direction cosines for ammonium sulfate single crystal, anisotropic peaks corresponding to $SO_4^-,\;SO_2^-$ and defect structure corresponding to electron excess type are identified.

• KSBB Journal
• /
• v.5 no.1
• /
• pp.81-85
• /
• 1990

Lignin was extracted from the rice straw by using the solvent mixture of buthyl alcohol and distilled water. And the experiment of vanillin production from extracted lignin was performed with the oxidation catalysts; CuO, Cu(OH)2 and CuSO4.5H2O. The optimum conditions of lignin extraction are the reaction temperature 12$0^{\circ}C$ and the mixture of 250mL buthyloloohol, 250mL, distilled water and 25g rice straw in the presence of 2.5g p-toluenesulfonic acid. The yield of vanillin from extracted lignin increased linearly with the increase of reaction temperature. And it increased with the order of Cu(OH)<$_2$ CuO$_4\cdot \;5H_2$Oas oxidation catalysts. The maximum yield of vanillin was 9% in the presence of 2.5%(w/v) CuSO$_4\cdot \;5H_2$O under the following conditions: temperature, 18$0^{\circ}C$; pressure, 13atm; pH 4.0 and reaction time, two hours.

• Nuclear Engineering and Technology
• /
• v.54 no.6
• /
• pp.2329-2333
• /
• 2022

Base metal corrosion forms a significant issue during the chemical decontamination of the primary coolant loop in nuclear power plants as it is directly related to the economic and safety viability of decommissioning. In this technical note, potentiodynamic evaluations of several base metals (304 stainless steel, SA106 Grade B carbon steel, and alloy 600) were performed to determine their corrosion behavior during the hydrazine (N₂H₄)-based reductive ion decontamination (HyBRID) process. The results suggested that N₂H₄ protected the surface of the base metals in the HyBRID solution, which is primarily composed of H₂SO₄. The corrosion resistance of the carbon steel was further improved through the addition of CuSO₄ to the solution. The corrosion rate of carbon steel in the H₂SO₄-N₂H₄-CuSO₄ solution was lower than that exhibited in an oxalic acid solution, a commonly used reaction medium during commercial decontamination processes. These results indicate the superiority of the HyBRID process with respect to the base metal stability.

• Bulletin of the Korean Chemical Society
• /
• v.27 no.12
• /
• pp.1989-1996
• /
• 2006

The $NiSO_4/CeO_2-ZrO_2 $catalysts containing different nickel sulfate and $CeO_2$ contents were prepared by the impregnation method, where support, $CeO_2-ZrO_2$was prepared by the coprecipitation method using a mixed aqueous solution of zirconium oxychloride and cerium nitrate solution followed by adding an aqueous ammonia solution. No diffraction line of nickel sulfate was observed up to 20 wt %, indicating good dispersion of nickel sulfate on the surface of $CeO_2-ZrO_2$. The addition of nickel sulfate (or $CeO_2$) to $ZrO_2$ shifted the phase transition of $ZrO_2$ from amorphous to tetragonal to higher temperatures because of the interaction between nickel sulfate (or $CeO_2$) and $ZrO_2$. A catalyst (10-$NiSO_4/1-CeO_2-ZrO_2$) containing 10 wt % $NiSO_4$ and 1 mole % $CeO_2$, and calcined at $600{^{\circ}C}$ exhibited a maximum catalytic activity for ethylene dimerization. The catalytic activities were correlated with the acidity of catalysts measured by the ammonia chemisorption method. The role of $CeO_2$was to form a thermally stable solid solution with zirconia and consequently to give high surface area, thermal stability and acidity of the sample.

• Journal of Conservation Science
• /
• v.22
• /
• pp.121-134
• /
• 2008

The mechanism of stone exfoliation and its cause in relation to chemical weathering by soluble salt were studied. Chemical, mineralogical and physical analysis was performed in exfoliation samples from stone monuments. The representative salt is gypsum in the exfoliation samples. In order to understand the salt reaction, stone samples(tuff and granite) were treated with two type of the salt, gypsum and sodium sulfate, which have different solubility. The capillary water uptakes are slight increased in impregnated with Na2SO4 and weathering simulation of two rock types. It means that the rock is deteriorated in the near of the surface by $Na_2SO_4$. $CaSO_4{\cdot}2H_2O$ bring out the thicker exfoliation than $Na_2SO_4$ because it is penetrated into the deeper zone and amount of accumulated salt is more abundant in the inner part than in the near of the surface. The exfoliation was formed in the tuff by salt treatment and 30cycle of weathering simulation, but there are not significant symptoms of exfoliation in the granite by same condition. This result was caused by the different capillary water uptakes and porosity of the rocks. In the tuff, salt solutions are penetrated into the inner part due to its high capillary water uptakes and porosity but the granite, which has low value relatively, can be formed thinner exfoliation.

• Journal of the Korea Organic Resources Recycling Association
• /
• v.28 no.3
• /
• pp.5-14
• /
• 2020

This study aims to survey the effect of sulphuric acid (H₂SO₄) treatment for pH adjustment with 6.5 and 7.0 regarding ammonia volatilization on chemical content change in the aerobic liquefying process of co-digesate swine manure and apple pomace. The digestates of swine manure was aerated with 0.3 ㎥ air/㎥·min for 60 days. The untreated digestate showed the increased pH and decreased contents of electrical conductivity (EC) and total nitrogen (T-N). The untreated digestate had a high concentration of NH₃ with 172.6 mg/L, but, ammonia (NH₃) concentration of H₂SO₄-treated digestate was significantly lower than that of untreated digestate. The H₂SO₄-untreated digestate for retaining aeration showed a decreased concentration of 47.2% of ammonium nitrogen. While, the H₂SO₄-treated digestate had a high concentration of ammonium nitrogen compared to the untreated digestate. Also, the H₂SO₄ treatment affected to increase the contents of nitrogen and phosphoric acid content. Therefore, the pH adjustment with H₂SO₄ might be a useful method for the decreased ammonia concentration and nitrogen maintenance in the aerobic liquefying process of swine manure digesate.

• Journal of Korean Society of Environmental Engineers
• /
• v.30 no.9
• /
• pp.918-924
• /
• 2008

This research investigates the influences of the presence of aquatic macrophytes on the changes of biogeochemistry in the sediments through the comparative analysis of porewater and sediments. From the in situ measurements, elevated SO$_4{^{2-}}$ concentrations were observed in the rhizosphere during the growing season, which was resulted from the oxidation of reduced sulfide in the sediments by the oxygen release from the plant roots. There was sufficient AVS in the sediments to induce observed SO$_4{^{2-}}$ concentrations. The amount of oxygen in the oxidation of AVS to produce observed SO$_4{^{2-}}$ concentrations is 0.85 g/m$^2$ day which is relevant to the results of other researches. The AVS concentrations in the vegetated sediments increased with the depth whereas there is higher mass of AVS in the surface of the non-vegetated sediments. This shows that evapotranspiration induces the transportation of SO$_4{^{2-}}$ in the surface water into the anaerobic sediments. In addition, the elevated organic content caused by the presence of plants increased $\beta$-glucosidase activities which play an important role in the carbon cycle of the sediments.

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

• Korean Chemical Engineering Research
• /
• v.51 no.2
• /
• pp.195-202
• /
• 2013

$TiO_2$ powders were prepared from titanium (IV) sulfate ($Ti(SO_4)_2$) solution using ammonia solution at low reaction temperature ($80{\sim}100^{\circ}C$) and atmospheric pressure by hydrothermal precipitation method without calcination. The effect of reaction conditions, such as reaction temperature, initial concentration of titanium (IV) sulfate ($Ti(SO_4)_2$) solution, pH of mixture solution and the physical properties of the prepared $TiO_2$, such as crystallite structure, crystallite size were investigated. The photocatalytic activity of prepared $TiO_2$ was tested by the photolysis of brilliant blue FCF (BB-FCF) under the UV and the analysis of UV-VIS diffuse reflectance spectroscopy (DRS). The physical properties of prepared $TiO_2$ were examined by X-ray diffraction (XRD), scanning electron microscopy (SEM), photoluminescence spectrometer (PL), particle size distribution measurements. The crystallite size and crystallinity of prepared $TiO_2$ increased with increasing titanium (IV) sulfate ($Ti(SO_4)_2$) concentration, but photocatalytic activity decreased. The crystallite size decreased with increasing pH of mixture solution, but photocatalytic activity increased. The crystallinity and photocatalytic activity increased with increasing reaction temperature. The results showed that anatase type $TiO_2$ could be prepared by hydrothermal precipitation method using titanium (IV) sulfate ($Ti(SO_4)_2$) solution and ammonia solution at low reaction temperature and atmospheric pressure without calcination.