The simulated dyes solution containing Basic Red 46(BR 46), Yellow 21(Y 21), and Maxilon Blue 30(MB 30) were electrochemically oxidized using carbon fiber as an anode. The electrolyses were performed in a electrolytic flow cell constructed by Vycor glass tube. The carbon fiber was positioned in the inside of Vycor glass tube and platinum wire coiled around outside of tube as a cathode. Several operating variables, such as current, time, pH and flow rate of solution were studied. Increasing current density would lead to a corresponding increase in the dye removal efficiency 99.2 % at a 200 mA. The electrolyses time could also improve and removal efficiency was about 99 % after 1.5 hours of electrolyses. The removal efficiency was increased with the increase of flow rate of solution and optimum flow rate was 5 mL/min. THe pHs of solution affect the removal efficiency. The removal efficiency was decreased with the increase of pH of solution and optimum pH was 5.05 (0.1 M KNO3).

The adsorption behavior of Eosin Y on activated carbon (AC) in batch system was investigated. The adsorption isotherm could be well fitted by the Langmuir adsorption equation. The kinetics of adsorption followed the pseudo-second-order model. The temperature variation was used to evaluate the values of free energy (ΔG°), enthalpy (ΔH°) and entropy (ΔS°). The positive value of enthalpy change ΔH° for the process confirms the endothermic nature of the process and more favourable at higher temperature, the positive entropy of adsorption ΔS° reflects the affinity of the AC material toward Eosin Y and the negative free energy values ΔG° indicate that the adsorption process is spontaneous. With the increase of the amount of AC, removal efficiency of Eosin Y was increased, but adsorption capacity was decreased. And adsorption capacity was increased with the decrease of particle size. With the increase of the amount of AC, removal efficiency of Eosin Y was increased, but adsorption capacity was decreased. And adsorption capacity was increased with the decrease of particle size.

The aim of this research was to evaluate the performance of insoluble electrode for the purpose of degradation of Rhodamine B (RhB) and oxidants generation [N,N-Dimethyl-4-nitrosoaniline (RNO, indicator of OH radical), O3, H2O2, free Cl, ClO2)]. Methods: Four kinds of electrodes were used for comparison: DSA (dimensional stable anode; Pt and JP202 electrode), Pb and boron doping diamond (BDD) electrode. The effect of applied current (0.5～2.5 A), electrolyte type (NaCl, KCl and Na2SO4) and electrolyte concentration (0.5～3.5 g/L) on the RNO degradation were evaluated. Experimental results showed that the order of RhB removal efficiency lie in: JP202 > Pb > BDD ≒> Pt. However, when concerned the electric power on maintaining current of 1 A during electrolysis reaction, the order of RhB removal efficiency was changed: JP202 > Pt ≒ Pb > BDD. The total generated oxidants (H2O2, O3, free Cl, ClO2) concentration of 4 electrodes was Pt (6.04 mg/W) > JP202 (4.81 mg/W) > Pb (3.61 mg/W) > BDD (1.54 mg/W), respectively. JP202 electrode was the best electrode among 4 electrodes from the point of view of performance and energy consumption. Regardless of the type of electrode, RNO removal of NaCl and KCl (chlorine type electrolyte) were higher than that of the Na2SO4 (sulfuric type electrolyte) RNO removal. Except BDD electrode, RhB degradation and creation tendency of oxidants such as H2O2, O3, free Cl and ClO2, found that do not match. RNO degradation tendency were considered a simple way to decide the method which is simple it will be able to determinate the electrode where the organic matter decomposition performance is superior. As the added NaCl concentration was increases, the of hydrogen peroxide and ozone concentration increases, and this was thought to increase the quantity of OH radical.

The purpose of this study is to investigate electro-generation of free Cl, ClO2, H2O2 and O3 and degradation of Rhodamine B in solution using Ru-Sn-Sb electrode. Electrolysis was performed in one-compartment reactor using a dimensionally stable anode(DSA) of Ru-Sn-Sb/Ti as the working electrode. The effect of applied current (0.5-3 A), electrolyte type (NaCl, KCl, HCl, Na2SO4 and H2SO4) and concentration (0.5-2.5 g/L), air flow rate (0-3 L/min) and solution pH (3-11) was evaluated. Experimental results showed that concentration of 4 oxidants was increased with increase of applied current, however optimum current for RhB degradation was 2 A. The generated oxidant concentration and RhB degradation of the of Cl type-electrolyte was higher than that of the sulfate type. The oxidant concentration was increased with increase of NaCl concentration and optimum NaCl dosage for RhB degradation was 1.75 g/L. Optimum air flow rate for the oxidants generation and RhB degradation was 2 L/min. ClO2 and H2O2 generation was decreased with the increase of pH, whereas free Cl and O3 was not affected by pH. RhB degradation was increase with the pH decrease.

The aim of this research was to apply experimental design methodology in the optimization condition of electrochemical oxidation of Rhodamine B(RhB). The reactions of electrochemical oxidation were mathematically described as a function of parameters amounts of current, NaCl dosage, pH and time being modeled by the use of the central composite design, which was used for fitting quadratic response surface model. The application of response surface methodology using central composite design(CCD) technique yielded the following regression equation, which is an empirical relationship between the removal efficiency of RhB and test variable in actual variables: RhB removal (%) = 3.977 + 23.279․Current + 49.124․NaCl － 5.539․pH － 8.863 ․time － 22.710․Current․NaCl + 5.409․Current․time + 2.390․NaCl․time + 1.061․pH․time － 0.570․time2. The model predicted also agree with the experimentally observed result(R2 = 91.9%).

본 연구에서는 금 나노입자 콜로이드를 이용하여 safranin-O의 광촉매적 분해를 관찰하였다. 금 나노입자는 용액상에서 safranin-O의 분해 속도를 빠르게 하기 위해서 사용되었다. 금 나노입자 콜로이드는 수용액상에서 Na₂CO₃ 와 PVP 고분자(poly(vinyl pyrrolidone))를 이용하는 환원방법에 의하여 제조하였다. Safranin-O의 분해현상은 자외선(UV light)와 과산화수소(H₂O₂)의 존재 하에서 금 나노입자 콜로이드와 염화금의 농도, 반응계의 산도(pH), 반응시간과 같은 실험조건들의 조절을 통해 연구되었다. 분해반응에 사용된 금 나노입자 콜로이드의 농도가 증가함에 따라서 염료가 분해되는 속도가 증가하였다. Safranin-O의 광산화 반응은 광학적으로 측정되었고, 금 나노입자의 기본적인 물성과 촉매 특성은 UV-Vis 광학계를 이용하여 측정되었다.

The photocatalytic decolorization of Rhodamine B (RhB) was studied using packed-bed reactor and immobilized TiO2/UV System. The 20 W UV-A, UV-B and UV-C lamps were employed as the light source. The effect of shape and surface polishing extent of reflector, distance between the reactor and reflector, reactor material were investigated. The results showed that the order of the initial reaction constant with reflector shape was round > polygon > W > rhombus. The optimum distance between the reactor and reflector was 2 cm. The initial reaction constant of quartz reactor was 1.46 times higher than that of the PVDF reactor.

This study was conducted to select the most suitable dye bath soil of mat rush for good quality. Dry stem weight ranged from 102.5 to 107.0 g, dry stem ratio ranged from 34 to 36%, color of stem ranged from soft gray to heavy gray, degree of softness ranged from high to low and degree of floating ranged from extremely high to low. All the good quality components, such as dry stem weight, dry stem ratio, color of stem, degree of softness and degree of floating showed large variations. Hadong white ceramic soil, the superior dye bath soil of mat rush, showed relatively superior values for all the good quality components with 102.5 g in light dry stem weight, 34% in high dry stem ratio, good color of soft gray in color stem, high in degree of softness and extremely high id degree of floating. The results indicate that dye bath soils shows different adaptabilities to a particular dye bath and Hadong white ceramic soil seems to be the most suitable dye bath soil of mat rush for good quality.

천연 갈색 염모제를 개발하기 위하여 한국자생 거북꼬리 추출물로 염색한 머리카락의 염색성 조사와 함께 세정횟수에 따른 색깔변화를 화학 염모제로 염색한 머리카락과 비교하였다. 거북꼬리 추출물로 머리카락을 염색한 결과 대조구에 비해 δE값이 11이상 나타났으며, 모두 YR계열로 염색이 되었다. 매염제 처리에 따른 δE 값은 사스레피나무 회즙을 사용했을 때 15.52로 가장 크게 나타났다. 거북꼬리 추출물로 머리카락을 염색 후 세정 횟수에 따른 L값은 사스레피나무 회즙처리구에서 가장 낮았고, a, b 및 δ 값은 사스레피나무 회즙처리구에서 가장 높게 나타났다. 염색한 머리카락을 30회 세정한 결과 L값은 화학염모제로 염색한 머리카락 보다 거북꼬리 추출물(사스레피나무 회즙 매염)로 염색한 것에서 낮게 나타났다. 염색한 머리카락의 세정횟수에 따른 a, b, 및 δE값의 변화는 화학염모제로 염색한 머리카락 보다 거북꼬리 추출물(사스레피나무 회즙 매염)로 염색한 것에서 적게 나타났다. 따라서 거북꼬리 추출물은 천연 갈색 염모제로서 실용성이 있는 것으로 나타났다.

The degradation of Rhodamine B (RhB) in water was investigated in laboratory-scale experiments, using five advanced oxidation processes (AOPs): UV/H2O2, fenton, photo-fenton, UV/TiO2, UV/TiO2/H2O2. The photodegradation experiments were carried out in a fluidized bed photoreactor equipped with an immersed 32 W UV-C lamp as light source. Initial decolorization rate and COD removal efficiency were evaluated and compared. The results obtained showed that the initial decolorization rate constant was quite different for each oxidation process. The relative order of decolorization was: photo-fenton > UV/TiO2/H2O2 > fenton > UV/H2O2 > UV/TiO2 > UV > H2O2. The relative order of COD removal was different from decolorization: photo-fenton ≒ UV/TiO2/H2O2 > UV/TiO2 > fenton > UV/H2O2. The photo-fenton and UV/TiO2/H2O2 processes seem to be appropriate for decolorization and COD removal of dye wastewater.

A magenta azomethine dye(D) was synthesized from the reaction of 3-methyl-1-phenyl-2-pyrazoline-5-one with N,N-diethyl-1,4-phenylenediamine. The magenta azomethine dye was identified on the basis of elemental analysis, 13C-NMR, infrared, and GC/MS studies. The magenta azomethine dye was decomposed in a basic solution. Rate constants of the fading reaction of magenta azomethine dye in ethanol-water solvent were measured spectrophotometrically at 540 nm. Reaction rate was increased with the increase of [OH-] and [H2O] in the region of [H2O]= 11～40 M. The reaction was governed by the following rate law. -d[D]/dt = {ko + kOH[OH-][H2O]}[D] A possible mechanism consistent with the empirical rate law has been proposed.

The photocatalytic decolorization of Rhodamine B (RhB) was studied using immobilized TiO2 and fluidized bed reactor. Immobilized TiO2(length: 1～2 mm, width: 1～3 mm, thickness: 0.5～2 mm) onto silicone sealant was employed as the photocatalyst and a 30 W germicidal lamp was used as the light source and the reactor volume was 4.8 L. The effects of parameters such as the amounts of photocatalyst, initial concentration, initial pH, superficial velocity, H2O2 and anion additives. (NO3-, SO42-, Cl-, CO32-) The results showed that the optimum dosage of the immobilized TiO2 were 87.0 g/L. Initial removal rate of RhB of the immobilized TiO2 was 1.5 times higher than that of the powder TiO2 because of the adsorption onto the surface of immobilized TiO2. In the conditions of acidic pH, initial reaction rate was increased slowly and reaction time was shorted. The effect of anion type on the reaction rate was not much.

Dye wastewater was treated by using an electrochemical oxidation process. Various combinations of electrodes such as carbon, Al and Fe were investigated. In this study, electrode material, electrolyte concentration, electrode distance, current density, and pH value were found to have significant effect on both pollutant removal efficiency and current efficiency in electrochemical oxidation process. After electrolysis for 40min with carbon/Al, it was observed that COD, T-N, NH4+ -N and color of treated wastewater were reduced from 580㎎/ℓ to 145㎎/ℓ, 67.2㎎/ℓ to 26.8㎎/ℓ, 46.8㎎/ℓ to 1.4㎎/ℓ, and 4200 Pt-Co units to 336 Pt-Co units, respectively. The optimal conditions of the electrooxidation process to treat the wastewater for this study were found to be such as : current density ; 16.67mA/㎠, electrode distance ; 2.5cm, pH value ; 5.0 and carbon/Al electrode.

(1-3)-β-glucanase 동위효소의 발현 양상을 등 전점 전기영동 젤에서 직접 검출 확인할 수 있는 방법을 개발하였다. 개발된 방법은 시판되고 있는 (1-3)-β-glucanase활성 측정용 염료착색 기질을 이용하였다. 본 방법은 신속, 간편하며 보리 종자에서 발현되는 것으로 알려져 있는 모든 (1-3)-βglucanase 동위효소를 검출할 수 있을 정도로 민감하고 특이적이었다. 시판되고 있는 Penicillium(1-3)-β-glucanase에 대한 활성 검출 한계단위는 50 u U 정도로 추정되었다. 따라서, 본 방법은 특별한 시설이나 연구 인력을 확보하고 있지 않는 연구실에서 식물체의 (1-3)-β-glucanase발현에 대한 단백질 수준에서의 연구를 수행하는데 유용하게 이용될 수 있을 것으로 생각된다