• 한국대기환경학회지
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• 제20권5호
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• pp.593-601
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• 2004

In this study, we are going to compare the chemical composition of the precipitation that falls in the Dangjin and Anmyon-do areas by analyzing the water soluble components (anion and cation). We also examined the effects of seasonal change and regional difference in those data sets. The [$NO_3\;^- \;+\;SO_4\;^{2-}$] at 49.2${\mu}$eq/l is 67% of the total anion of 73.1${\mu}$eq/l, while that of [$NH_4\;^+\;+\;Ca^{2+}$] at 37.7${\mu}$eq/l is 62% of the cation in Dangjin area. Also, the [$NO_3\;^-\;+\;SO_4\;^{2-}$] concentration of 151.8 (${\mu}$eq/l) is 62% for the total anion of 143.5 (${\mu}$eq/l), and the [$NH_4\;^+\;+\;Ca^{2+}$] concentration of 119.7 (${\mu}$eq/l) is 47% for the cation of 254.3 (${\mu}$eq/l) in Anmyon-do area. The ion composition ratio is shown for the order by 22% of $SO_4\;^{2-}$, 20.8% of $NH_4\;^+$ and 15.4% of $Cl^-$ that is the sum of 58.7% for the total ion composition in Dangjin area, and is the order by 33.8% of $NH_4\;^+$, 16.3% of $SO_4\;^{2-}$ and 11.1% of $Cl^-$ in Anmyon-do area. Furthermore, We predicted that even areas which were previously clean will get acid rain if there is large scale construction there or nearby.

• 공업화학
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• 제10권1호
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• pp.51-57
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• 1999

원자로 정지시 냉각제 계통내 탈염 공정의 최적운전에 도움을 줄 목적으로 Amberite IRN 77 양이온 교환수지상에서 Ni(II), Co(II) 및 Ag(I) 이온의 흡착특성을 연구하였다. 양이온 교환수지상에서 Ni(II), Co(II) 및 Ag(I) 이온 각각의 흡착 메카니즘은 Langmuir isotherm에 잘 일치하였다. 양이온교환수지의 형태에 따른 영향으로서 $H^+$-형의 수지의 흡착 및 처리 용량은 $Li^+$-형의 수지보다 우수하였다. 다성분계의 용액을 위한 연속식 이온교환공정에서 양이온교환수지의 흡착선택성은 Ni(II)${\approx}$Co(II)>Ag(I)였으며, 유속의 증가는 수지의 처리용량 뿐만 아니라 파과곡선의 기울기를 감소시켰다.

• 폴리머
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• 제30권4호
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• pp.305-310
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• 2006

전자선 전조사를 이용하여 PE/PP와 PET 복합섬유 기재에 스티렌을 그래프트 공중합하여 복합양이온 교환 섬유를 합성하였다. 공중합체의 그래프트율은 스티렌 단량체의 농도가 80%일때 123%이었으며 설폰화율은 스티렌 농도 70%에서 3.3 mmol/g 이었으며 그 이후에서는 큰 변화가 없었다. 또한 섬유의 인장강도는 기재에 비해 모두 낮게 나타났으며, 공중합체보다 이온교환 섬유의 인장강도가 최대 $0.206kgf/mm^2$ 로 낮게 나타났다 이온교환 섬유의 칼슘 및 마그네슘 이온에 대한 흡착파과 시간은 pH, 온도가 증가할수록 길어졌으며, 혼합 용액의 경우 단일 용액에 비해 마그네슘의 흡착파과가 늦게 나타났다. 한편 칼슘 및 마그네슘에 대한 반응속도 상수는 각각 0.012, 0.011 L/mg.h 이었으며, 최대 이온교환 흡착용량은 각각 47.06, 42.83 mg/g, 활성화 에너지는 각각 2,169, 1,534 J/mol 이었다.

• The Korean Journal of Ecology
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• 제23권2호
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• pp.83-88
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• 2000

When interpreting change over time in forest ecosystems, distinguishing the effects of forest succession from the effects of environmental stress can be difficult. The result may be a simplistic interpretation. citing a specific successional or environmental cause of forest change when both types may be occurring. We present two case studies of changes in the forest floor in northern hardwoods. First, the belief that 50% of soil organic matter is lost in the first 20 years after logging was based on a study comparing northern hardwood stands of different ages. We resampled a series of 13 such stands after an interval of 15 years, and found that the young stands were not, in fact. losing organic matter as rapidly as predicted from the original chronosequence study. The pattern of higher organic matter content in the forest floors of older stands compared to young stands could be equally well explained by changes in logging practices over the last century as by the aging of the stand. The observed pattern of forest floor organic matter as a function of stand age was previously interpreted as a successional pattern, ignoring changes in treatment history. In the second case study, observed losses of base cations from the forest floor were attributed to cation depletion caused by acid rain and declining calcium deposition. We found that young stands were gaining base cations in the forest floor; losses of base cations were restricted to older stands. Differences in litter chemistry in stands of different ages may explain some of the pattern in cation gains and losses. In this case, the contribution of successional processes to cation loss had been overlooked in favor of environmental stress as the dominant mechanism behind the observed changes. Studies of environmental stress use repeated measures over time. but often don't consider stand age as a factor. Studies of successional change often assume that environmental factors remain constant. We were able to consider both forest succession and external factors because we repeatedly sampled stands of different ages.

• 전기화학회지
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• 제12권1호
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• pp.54-60
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• 2009

The redox characteristics of 2-arylaldehydehydrazono-3-phenyl-5-substituted-2, 3-dihydro-1, 3, 4-thiadiazoles (1a-h) have been investigated in nonaqueous solvents such as 1, 2-dichloroethane (DCE), dichloromethane (DCM), acetonitrile (AN), Tetrahydrofuran (THF), and dimethylsulfoxide (DMSO) at platinum electrode. Through controlled potential electrolysis, the oxidation and reduction products of the investigated compounds had been separated and indentified. The redox mechanism had been suggested and proved. It had been found that all the investigated compounds were oxidized in two irreversible one-electron processes following the well-known pattern of The EC-mechanism; the first electron loss gives the corresponding cation-radical which is followed by proton removal from the ortho-position in the N-phenyl ring forming the radical. The obtained radical undergoes a second electron uptake from the nitrogen in the N = C group forming the unstable intermediate (di-radical cation) which undergoes ring closure forming the corresponding cation. The formed cation was stabilized in solution through its combination with a perchlorate anion from the medium. On the other hand, these compounds are reduced in a single two-electron process or in a successive two one-electron processes following the well known pattern of the EEC-mechanism according to the nature of the substituent; the first one gives the anion-radical followed by a second electron reduction to give the dianion which is basic enough to abstract protons from the media to saturate the (C = O) bond.

• Journal of Advanced Marine Engineering and Technology
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• 제29권6호
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• pp.654-661
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• 2005

Copper is a well known alloying element that is used to improve the resistance to general corrosion of stainless steel And also Cu cation have the anti-fouling effect to inhibit adhesion of the marine algae and shellfish to the surface of heat exchanger cooling pipe or outside wall of the ship, Therefore there are some anti-fouling methods such as anti-fouling Paint mixed with copper oxide or MGPS(Marine Growth Preventing System) by using Cu cation dissolved to the sea wather solution. Cu cation can be dissolved spontaneously by galvanic current due to Potential difference between Cu and cooling pipe of heat exchanger with Ti material, which may be one of the anti-fouling designs. In this study the effect of annealing heat treatment to galvanic current and Polarization behavior was investigated with a electrochemical points of view such as measurement of corrosion Potential, anodic polarization curve. cyclic voltammetric curve, galvanic current etc The grain size of the surface in annealed at $700^{\circ}C$ was the smallest than that of other annealing temperatures. and also the corrosion Potential showed more positive potential than other annealing temperatures. The galvanic current between Ti and Cu with annealed at $700^{\circ}C$ was the largest value in the case of static condition. However its value in the case of flow condition was the smallest than the other temperatures. Therefore in order to increase anti-fouling effect by Cu cation, the optimum annealing temperature in static condition of sea water is $700^{\circ}C$, however non- heat treated specimen in the case of flow condition may be desirable.

• Asian-Australasian Journal of Animal Sciences
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• 제17권12호
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• pp.1712-1716
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• 2004

Copper-bearing montmorillonite (Cu-MMT) was produced by $Cu^{2+}$ cation exchange reaction. X-ray diffraction analysis showed that that the (001) basal spacing of the MMT crystal lattice increased from 1.544 to 1.588 nm after $Cu^{2+}$ exchange. This indicated that $Cu^{2+}$ entered into interlayer position of MMT as a hydrated cation or composite cation. In vitro results indicated that Cu-MMT had antibacterial activity on Escherichia coli $K_{88}$. Cu-MMT had unbalanced positive charge after cation exchange. Its antibacterial activity resulted from two aspects, one was electrostatic attraction which made E. coli $K_{88}$ being adhered on the montmorillonite surface, the other was the $Cu^{2+}$ slowly released, which could kill bacteria. In an in vivo study, four replicates of eight weanling pigs were assigned to each of two dietary treatments to study the effects of Cu-MMT on diarrhea, E. coli in the lumen of the jejunum and morphology of jejunal mucosa. As compared to the control, supplementation of the diet with 0.2% Cu-MMT improved average daily gain by 12.50% (p<0.05) and decreased F/G by 9.42% (p<0.05). The mean diarrhrea incidence was decreased by 71.80% (p<0.05). The viable counts of Escherichia coli in jejunal contents were significantly reduced (p<0.05). Villus height and the villus height to crypt depth ratio at the jejunal mucosa were increased by 19.09% (p<0.05) and 37.10% (p<0.05), respectively.

• 공업화학
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• 제3권2호
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• pp.240-246
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• 1992

X선 광전자분광법을 이용하여 교환된 제올라이트내 산소원자의 전자구조를 조사하였다. $Na^+$, $Fe^{2+}$ 및 $Fe^{3+}$로 교환된 X형 및 Y형 제올라이트에 대하여 얻어진 $O_{1S}$스펙트럼은 골격산소의 결합에너지를 밝히기 위하여 분해하였다. 각 스펙트럼에서는 2-3개의 분해띠들이 있었다. 분해된 각 띠들의 특성은 교환된 양이온에 따라서 $O_{1S}$ 전자의 결합에너지와 띠면적의 관점에서 고찰되었다. 분해된 띠들을 각각 골격내 가교산소에 의한 것(띠 1), 양이온에 결합된 산소에 의한 것(띠 2), 양이온에 배위된 물분자내 산소에 의한 것(띠 3)으로 해석되었다. $O_{1S}$스펙트럼 면적의 대부분을 차지하고 있는 띠 1은 제올라이트내 Al함량의 감소에 따라서 결합에너지상의 증가를 나타내었다.

• 공업화학
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• 제10권2호
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• pp.206-211
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• 1999

본 연구에서는 NaCl수용액의 초저이온 농도범위 ($1.0{\times}10^{-4}M$ 이하)에서 양이온 교환수지 대 음이온 교환수지의 비, 수지량, 계의 온도를 함수로 한 혼합층 이온교환의 거동을 실험적으로 연구하였다. 실험실 크기의 연속흐름 칼럼을 통하여 양이온 교환수지와 음이온 교환수지의 교환능이 소모될 때까지의 유출농도를 처리된 유량의 함수로 측정하여 파과곡선을 구하였다. 초기누출은 수지량이 적은 경우 양이온과 음이온의 파과곡선에 나타났으나, 선택도계수가 낮은 양이온의 파과곡선에 현격하게 크게 나타났다. 선택도계수는 파과곡선의 기울기에 영향을 미쳤으며, 계수값이 큰 음이온의 파과곡선의 기울기가 급격하였다. 온도변화는 파과곡선의 기울기에 영향을 미쳤으며, 온도가 증가할수록 이온교환속도가 증가하였다. 이 온도효과는 수지비에 관계없이 수지총량이 증가할수록 또는 이온교환수지의 교환능이 감소하여 파과곡선이 평형에 가까워질수록 감소하였다.

• 대한전기학회:학술대회논문집
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• 대한전기학회 2006년도 추계학술대회 논문집 전기물성,응용부문
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• pp.18-19
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• 2006

In this study, dielectric properties of the ${Mg_5}{B_4}{O_{15}}$ (B=Ta, Nb) cation-deficient perovskite ceramics and its oscillator application are investigated. The cation-deficient perovskite ceramics are prepared through the solid-state route. According to the XRD pattern, ${Mg_4}{Ta_2}{O_9}$ and $Mg{Ta_2}{O_6}$ phase existed in calcined and sintered ${Mg_5}{Ta_4}{O_15}$ powder. Also ${Mg_5}{Ta_4}{O_{15}}$ phase added with increasing sintering temperature. In the case of calcined and sintered ${Mg_5}{Nb_4}{O_{15}}$ powder, single phase of ${Mg_5}{Nb_4}{O_{15}}$ is appeared. In the case of the ${Mg_5}{Ta_4}{O_{15}}$ and ${Mg_5}{Nb_4}{O_{15}}$ ceramics sintered at $1450^{\circ}C$ for 5h, the dielectric constant, quality factor, and temperature coefficient of the resonant frequency (TCRF) were 8.2, 259,473 GHz, $-10.91ppm/^{\circ}C$ and 14, 37,350 GHz, $-52.3\;ppm/^{\circ}C$, respectively. Simulated DR with ${Mg_5}{Ta_4}{O_{15}}$ ceramics had the operating frequency of 10.99 GHz and S(2,1) of -29.795 dB. Size of manufactured oscillator was $56{\times}48{\times}34\;mm^3 and operated at 11.93 GHz. Power output and second harmonic of oscillator were +13.61 dBm and -23.81 dBc at 23.85 GHz, respectively.