• JSTS:Journal of Semiconductor Technology and Science
• /
• 제2권1호
• /
• pp.41-48
• /
• 2002

This paper presents a 18-mW, 2.5-㎓ fractional-N frequency synthesizer with l-bit $4^{th}$-order interpolative delta-sigma ($\Delta{\;}$\sum$)modulator to suppress fractional spurious tones while reducing in-band phase noise. A fractional-N frequency synthesizer with a quadruple prescaler has been designed and implemented in a $0.5-\mu\textrm{m}$ 15-GHz $f_t$ BiCMOS. Synthesizing 2.1 GHzwith less than 200 Hz resolution, it exhibits an in-band phase noise of less than -85 dBc/Hz at 1 KHz offset frequency with a reference spur of -85 dBc and no fractional spurs. The synthesizer also shows phase noise of -139 dBc/Hz at an offset frequency of 1.2 MHz from a 2.1GHz center frequency.

• 한국토양비료학회지
• /
• 제32권1호
• /
• pp.47-56
• /
• 1999

경기도 군포시 및 수원시에서 축산지역과 영농지역 및 주거지역의 토지이용방식을 반영하는 14곳의 지하수 과측정을 대상으로 1997년 1원부터 12월까지 지하수 시료를 채취하여 지하수질의 화학성과 질산태 질소농도를 소사한 결과 지하수의 양이온 조성은 토지이용방식에 따라 큰 차이가 없었지만, 음이온 조성에서는 축산지역 소재 지하수의 $NO{_3}^-$의 비율이 상대적으로 높았다. 영농지역 지하수의 질산태질소 농도는 영농활동의 영향으로 4월과 7월사이에서 증가하는 것으로 나타났으며, 축산지역 지하수는 강우유형에 영향을 받는 것으로 판단할 수 있었고 주거지역의 질산태질소농도는 시기에 상관없이 일정한 수준을 유지했다. 질산태 질소의 오염원을 구명하기 위해 Urea, Ammonium sulfate, 축산 폐수, 청정지역 지하수 중에 포함된 질소의 동위원소비를 측정한 결과 각각 +1.4, -2.7, +27.2, +5.5% 로 나타나 이 ${\delta}^{15}N$ 값을 근거로 지하수중 질산태질소의 ${\delta}^{15}N$ 값이 +5% 이하인 경우 화학비료영향 +5~+10‰은 토양 질소, +10‰ 이상은 축산폐수 또는 생활하수 영향으로 오염원 구분기준을 설정할 수 있었다. 관측정 지하수중 질산태 질소의 ${\delta}^{15}N$ 값은 대부분 토지이용방식에 따른 오염원을 반영했지만, 영농과 축산이 복합적으로 운영되는 농촌지역의 특성상 단일 오염원보다는 두 종류 이상의 오염원이 공동으로 지하수질에 영향을 미치는 것으로 판단할 수 있었다. 또한 각 오염원의 오염 기여도는 관측정 주위의 토지이용방식에 따라 차이가 있었지만, 같은 관측정 내에서도 시기에 따라 그 기여도가 변함을 알 수 있었다.

• 한국환경과학회지
• /
• 제28권1호
• /
• pp.7-18
• /
• 2019

This study aimed to assess the impact of livestock excreta discharged from an Intensive Livestock Farming Area (ILFA) on river water quality during a rainfall event. The Bangcho River, which is one of the 7 tributaries in the Cheongmi River watershed, was the study site. The Cheongmi River watershed is the second largest area for livestock excreta discharge in Korea. Our results clearly showed that, during the rainfall event, the water quality of the Bangcho River was severely deteriorated due to the COD, $NH_4-N$, T-N, $PO_4-P$, T-P, and heavy metals (Cu, Zn, and Mn) in the run-off from nearby farmlands, where the soil comprised composted manure and unmanaged livestock excreta. In addition, stable isotope analysis revealed that most of nitrogen ($NH_4-N$ and $NO_3-N$) in the run-off was from the ammonium and nitrate in the livestock excreta. The values of ${\delta}^{15}N_{NH4}$ and ${\delta}^{15}N_{NO3}$ for the Bangcho River water sample, which was obtained from the downstream of mixing zone for run-off water, were lower than those for the run-off water. This indicates that there were other nitrogen sources upstream river in the river. It was assumed from ${\delta}^{15}N_{NH4}$ and ${\delta}^{15}N_{NO3}$ stable isotope analyses that these other nitrogen sources were naturally occurring soil nitrogen, nitrogen from chemical fertilizers, sewage, and livestock excreta. Therefore, the use of physicochemical characteristics and nitrogen stable isotopes in the water quality impact assessment enabled more effective analysis of nitrogen pollution from an ILFA during rainfall events.

• 자원환경지질
• /
• 제45권1호
• /
• pp.23-30
• /
• 2012

농업지역인 충북 영동 지역 지하수의 지화학적 특성과 질산염의 기원을 규명하기 위하여 지화학 및 질소동위원소 연구가 수행되었다. 지하수의 pH는 평균 7.2 (6.0~8.2)로 약산성 내지 약알칼리성으로 나타났다. 지하수의 평균 전기전도도, 산화환원전위 및 용존산소량은 각각 369 ${\mu}S/cm$ (70~729 ${\mu}S/cm$), 165.6 mV (29-383.2 mV), 4.3 mg/L(1.8~8.0 mg/L)이다. 지하수 내 양이온을 함량이 높은 순으로 나열하면, $Ca^{2+}$>$Na^{2+}$>$Mg^{2+}$>$K^{2+}$이고, 음이온의 경우는 ${HCO_3}^-$>${NO_3}^-$>${SO_4}^{2-}$>$Cl^-$>$F^-$이다. 연구지역 지하수의 대부분은 물-암석과의 반응으로 기인된 Ca-$HCO_3$ 유형으로 나타났으며, Ca-Cl 유형 (2.5%) 과 Na-$HCO_3$ (2.5%) 유형은 농업활동 등의 영향으로 전이된 것으로 밝혀졌다. 지하수 내 질산성 질소의 함량은 10.2 mg/l~26.9 mg/l 범위로 검출되어 오염이 우려되는 것으로 밝혀졌다. 지하수 내 질산성 질소의 기원을 파악하기 위한 질소 동위원소 분석 결과, 질산성 질소의 동위원소비 (${\delta}^{15}N_{-}NO_3$)는 1.9‰~19.4‰ (평균 10.1‰)로 측정되었으며, 동위원소비에 따른 질산염의 기원은 축사의 동물 분뇨나 농지에 시비된 유기물 비료임을 나타낸다.

• 한국농공학회논문집
• /
• 제52권5호
• /
• pp.37-45
• /
• 2010

Manure recycling as fertilizer is one of solutions for the environmental problem related with livestock manure treatment as well as the ocean dumping ban act prohibiting manure disposal to the ocean. For the manure disposal, forest area can be a candidate place because the area has a wide range of applicable sites. However, the manure application to the forest has a possibility of causing environmental impacts including water quality problems due to nutrient loading. Therefore it is necessary to investigate water quality impact from manure disposal to the forestry plantation. In this study, ground and soil water quality had been monitored in the bio-circulation experimental forest where low concentration liquid manure (LCLM) was applied. Soil and groundwater samples were collected and analyzed weekly from April to October in 2008 and 2009. The mean and variation of NO3-N concentration in soil water of LCLM treatment places showed higher concentration than the reference places declining during growing season. In the case of groundwater from monitoring well in the downstream of disposal site, the $NO_3$-N concentration was 3.59 mg/L in 2008 and 3.26 mg/L in 2009 in average showing higher concentration than the reference well although the concentration was not exceed the national drinking water standard. To investigate the source of nitrate, $\delta^{15}N$ isotope analysis was also implemented. Its result showed that the LCLM application could be the nitrate source requiring further long-term monitoring soil and water quality.

• 대한지하수환경학회지
• /
• 제6권4호
• /
• pp.171-179
• /
• 1999

충북 초청지역에서 산출되는 탄산수는 낮은 pH(5.0~5.8), 높은 이산화탄소분압(about 1 atm, Pc $o_2$) 및 높은 총용존이온함량(＜989 mg/L, TDS)을 보이며. 화학적으로 Ca-HC $O_3$ 유형을 갖는 특징을 보인다. 산소. 수소안정동위원소 및 삼중수소 결과에 따르면 초정탄산수는 천수기원이며. 지표수나 천층지하수와 상당히 혼합된 특성을 보여준다. 탄소동위원소결과($\delta$$^{13}$ $C_{{\Sigma}CO2}$)는 탄산수(-8.6~-5.3$ extperthousand$, $\delta$$^{13}$C)는 심부기원으로부터 유래된 특성을 보여주며. 화강암지역 일반지하수 (-14.4~-6.8$\textperthousand$. $\delta$$^{13}$C)는 탄산수의 영향을 받았으며. 변성퇴적암지역 일반지하수(-17.9~-15.2$\textperthousand$. $\delta$$^{13}$C)는 토양기원탄소와 방해석과의 반응에 의해 조절된 특성을 보여준다. 황동위원소특성($\delta$$^{34}$ $S_{SO4}$＝＋3.5~＋11.3$\textperthousand$)은 탄산수와 지표수와의 혼합과정을 뒷받침해준다. 스트론튬동위원소비($^{87}$ Sr/$^{86}$Sr)는 탄산수(0.7138~0.7156)는 천매암중의 방해석(0.7281~0.7346) 또는 부악광산의 방해석(0.7184)과의 반응과는 무관함을 보여준다. 또한 질소동위원소($\delta$$^{15}$ $N_{NO3}$)를 통하여 탄산수내 높은 함량의 질산염(최대 55.0 mg/L, N $O_3$) 기원으로서는 비료와 축산분뇨임을 확인할 수 있었으며. 질소순환과정에서 탈질산화작용이 수반되었을 가능성을 보여준다. 초정지역 탄산수에 대한 수리화학자료와 각종 동위원소자료를 근거로 초정지역 탄산수에 대한 가능한 직화학적 진화모델을 설정하였다. 탄산수는 심부기원의 $CO_2$의 공급으로 형성된 탄산수가 화강암과의 반응을 통해서 진화되었으며. 이러한 탄산수는 천부로 상승하는 과정에서 지표기원의 지하수와 상당히 혼합되어 형성되었음을 지시한다.시한다.

• Bulletin of the Korean Chemical Society
• /
• 제24권3호
• /
• pp.350-356
• /
• 2003

The mechanism of the decomposition of a bronchodilator, S-nitroso-N-acetyl-D,L-penicillamine (SNAP) by a bronchoconstrictor, aqueous sulfite, has been investigated in detail. The decomposition was studied using a conventional spectrophotometer at 336 nm over the ranges: 0.010 ≤ $[S^{IV}]_T$ ≤ 0.045 mol $dm^{-3}$, 3.96 ≤ pH ≤ 6.80 and 15.0 ≤ θ≤ 30.0 ℃, 0.60 ≤ I ≤ 1.00 mol $dm^{-3}$, and at ionic strength 1.00 mol $dm^{-3}$ (NaCl). The rate of reaction is dependent on the total sulfite concentration and pH in a complex manner, i.e., $k_{obs}\;=\;k_1K_2[S^{IV}]_T/ ([H^+]\;+\;K_2)$. At 25.0 ℃, the second order rate constant, $k_1$, was determined as $12.5\;{\pm}\;0.15\;mol^{-1}\;dm^3\;s^{-1}$. ${\Delta}H^{neq}\;=\;+32\;{\pm}\;3 kJ\;mol^{-1}\;and\;{\Delta}S^{\neq}\;=\;-138\;{\pm}\;13\;J\;mol^{-1}K^{-1}$. The N-nitrosohydroxylamine-N-sulfonate ion was detected as an intermediate before the formation of any of the by-products, namely, N-acetyl-D,L-penicillamine. The effect of concentration of aqueous copper(Ⅱ) ions on this reaction was also examined at pH 4.75, but there was no dependence on $[Cu^{2+}]$. In addition, the $pK_a$ of SNAP was determined as 3.51 ± 0.06 at 25.4 ℃ [I = 1.0 mol $dm^{-3}$ (NaCl)].

• Transactions on Electrical and Electronic Materials
• /
• 제15권4호
• /
• pp.226-229
• /
• 2014

In this study, lead-free $(Ba_{0.85}Ca_{0.15})(Ti_{1-x}Zr_x)O_3$ ceramics and a bimorph-type piezoelectric actuator were fabricated using the normal oxide-mixed sintering method, and their dielectric properties, microstructure, and displacement properties were investigated. From the results of X-ray diffraction, the pattern of the specimen has a pure perovskite structure. In addition, no secondary impurity phases were found. The excellent piezoelectric coefficient of $d_{33}=454pC/N$, the electromechanical coupling factor $k_p=0.51$, the dielectric constant ${\varepsilon}_r=3,657$, the mechanical quality factor $Q_m=239$, and $T_c$(Tetragonal-Cubic) =$90^{\circ}C$ were shown at x= 0.085. ${\Delta}k_p/k_p20^{\circ}C$ and ${\Delta}f_r/f_r20^{\circ}C$ showed the maximum value of -0.255 and 0.111 at $-20^{\circ}C$ and $80^{\circ}C$, respectively. The maximum total-displacement was $60{\mu}m$ under the input voltage of 50 V. As a result, it is considered that lead-free $(Ba_{0.85}Ca_{0.15})(Ti_{1-x}Zr_x)O_3$ ceramics is a promising candidate for piezoelectric actuator application for x= 0.085.

• 한국군사과학기술학회지
• /
• 제3권1호
• /
• pp.164-175
• /
• 2000

Three compounds of Cu(II)-loaded N,N,N'-trimethylethylenediaminated Merrifield-type polymers were synthesized with yields higher than 80%, and the hydrolysis reaction rates of O-isopropylmethyl-phosphonofluoridate(GB) and O-pinacolylmethylphosphonofluoridate (GD) catalyzed by them have been surveyed. GB and GD hydrolysis by Cu(II)-loaded polymers occurs via intermediate complex mechanism where rapid equilibrium to form intermediate complex between substrate and Cu(II)-loaded polymers($K_f$) is followed by rate determining hydrolysis step($k_1$). The measured activation parameters for $k_1$ are ${\Delta}H^{\ddag}$ : $17.75{\pm}0.98kJ/mol$ ${\Delta}S^{\ddag}$ / : $-218.42{\pm}3.35J/mol$ K, $E^{\circ}_a$ : $20.22{\pm}0.98kJ/mo1$ for GB and ${\Delta}H^{\ddag}$ / : $11.16{\pm}1.15kJ/mol,$${\Delta}S^{\ddag}$ /: $-258.57{\pm}3.93J/mol$ K, $E^{\circ}_a$ : $13.64{\pm}1.15 kJ/mol$ for GD. Standard enthalpy/entropy changes corresponding to the intermediate complex formation constant $K_f$ are ${\Delta}H^{\circ}$ : $37.05{\pm}2.19 kJ/mo1,$$ {\Delta}S^{\circ}$ : $163.12{\pm}7.49 J/mol$ K and ${\Delta}H^{\circ}$ : 418.59{\pm}2.04 kJ/mol,$ ${\Delta}S^{\circ}$ : 4111.92{\pm}6.98 J/mol$ K for GB and GD, respectively, The electron push-pull mechanism by Cu(II)-loaded polymers lowers the P-F bond breaking energy(~400 kJ/mol) to less than 1/20 compared to the case in which no Cu(II)-loaded resin presents. Analysis of $K_f$ and 4k_1$ over pH=6.5~8.0 range suggest that the GB and GD hydrolysis occurs intramolecularily with $pK_a$ =7.29 for ligated $H_2O$ and $t_{1/2}$=36.9 sec, $pK_a$ = 7.06 and $t_{1/2}$=177.7 sec for GB and GD, respectively.

• 한국지하수토양환경학회지:지하수토양환경
• /
• 제22권1호
• /
• pp.1-12
• /
• 2017

Nitrate ($NO_3^-$), a common surface water and groundwater pollutant, poses a serious environmental problem in regions with intensive agricultural activities and dense population. It is thus important to identify the source of nitrate contamination to better manage water quality. Due to the distinct isotope compositions of nitrate among different origins, the dual isotope analysis (${\delta}^{15}N$ and ${\delta}^{18}O$) of nitrate has been widely applied to track contamination sources. This paper provided the underlying backgrounds in the isotope analysis of nitrate, which included typical ranges of ${\delta}^{15}N$ and ${\delta}^{18}O$ from various nitrate sources, isotope fractionation, the analytical methods used to concentrate nitrate from samples, and the potential limitations of the dual isotope analysis along with the resolutions. To enhance the applicability of the dual isotope analysis as well as increase the ability to interpret field data, this paper also introduced several case studies. Furthermore, other environmental tracers including ${\delta}^{11}B$ and $Cl^-/Br^-$ ratios were discussed to accompany the dual isotope analysis for better assignment of contamination sources even when microbial transformation of nitrate and/or mixing between contaminant plumes occur.