• 한국통신학회논문지
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• 제33권3C호
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• pp.271-280
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• 2008

M채널 NPR(Near-Perfect Reconstruction) pseudo-QMF(Quadrature Mirror Filter) 뱅크의 설계는 일반적으로 SF(Spectral Factorization) 접근 방식을 혼합하여 많이 사용하며, 분리와 합성 필터들은 프로토타입 저역통과 필터(prototype lowpass filter : p-LPF)를 코사인 변조하여 사용한다. 그러나 이 방식은 $2M^{-th}$ 대역 필터 $G(z)=z^{-(N-1)}H(z^{-1})H(z)$의 SF 방식에 의해 p-LPF H(z)을 설계하기 때문에 p-LPF가 선형위상을 갖지 못할 뿐만 아니라 진폭왜곡이 최적화되지도 않았다. 따라서 대부분의 방법들이 재생 진폭왜곡 보다는 중첩상쇄왜곡을 줄이기 위한 p-LPF 설계를 제안하였다. 본 논문에서는 NPR pseudo-QMF 뱅크 구현에 필요한 p-LPF 설계를 위해 폐쇄형전달함수를 갖는 선형위상의 Maxflat(maximally flat) FIR 필터를 이용하는 새로운 방식을 제안하였다. 또한 폐쇄형주파수함수를 이용하여 $2M^{-th}$ 대역 필터 $G(z)=H^2(z)$로 표현되는 2M개 채널들의 전체진폭응답이 단일응답을 갖도록 p-LPF H(z)을 최적화하는 방법이 제안되었다. 실험 결과 시스템 최대진폭 왜곡이 $3.5{\times}10^{-4}\;({\simeq}-70dB)$보다 적고 각 분리 및 합성 필터들의 저지대역 감쇠가 -100dB 이상의 매우 뛰어난 NPR pseudo-QMF 뱅크 설계가 가능함이 증명되었다.

• 대한수학회논문집
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• 제34권4호
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• pp.1049-1067
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• 2019

In this paper, we discuss the number of distinct fuzzy subgroups of the group ${\mathbb{Z}}_{p^n}{\times}{\mathbb{Z}}_{q^m}{\times}{\mathbb{Z}}_r$, m = 1, 2, 3 where p, q, r are distinct primes for any $n{\in}{\mathbb{Z}}^+$ using the criss-cut method that was proposed by Murali and Makamba in their study of distinct fuzzy subgroups. The criss-cut method first establishes all the maximal chains of the subgroups of a group G and then counts the distinct fuzzy subgroups contributed by each chain. In this paper, all the formulae for calculating the number of these distinct fuzzy subgroups are given in polynomial form.

• 한국지반공학회논문집
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• 제36권3호
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• pp.15-23
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• 2020

지표면에서의 지반운동을 예측하는 지반운동예측모델은 30m까지의 평균전단파속도인 V_S30을 부지효과를 나타내는 주요한 변수로 사용한다. V_S30은 만약 V_S주상도 깊이(z)가 30m 이상이면 주상도로부터 바로 계산할 수 있다. 하지만, 모든 부지에서 z가 30m 까지 있는 것은 아니다. 따라서, z < 30m일 경우 30m까지 연장하는 모델로부터 V_S30을 예측할 필요가 있다. 이번 연구에서는 국내 지반 환경에 맞게 z가 30m 미만인 부지에서 V_S30을 추정하는 예측 모델에 대한 새로운 계수를 제안하였다. 분석 자료로 기상청과 국토지반정보 통합DB센터에서 획득한 297개의 V_S주상도를 활용하였고, 선행연구에서 제안한 식의 계수들을 회귀분석을 통해 새롭게 제시하였다. 분석 결과, z ≥ 15m 일 경우 대수로그 잔차의 표준편차가 약 0.061이내이므로 신뢰성 높은 V_S30를 예측하는 것으로 확인하였다. z < 15m 일 경우 σ가 계속 증가하며, z = 5m일 경우 σ = 0.1으로 나타났다. 따라서, 매우 얕은 심도의 V_S주상도를 모델에 적용하는 경우 주의를 요하며, 가능하다면 30m깊이까지 지반조사를 실시하여 V_S30을 계산하는 것을 추천한다.

• 농약과학회지
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• 제2권3호
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• pp.79-84
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• 1998

콩나물중 carbendazim 잔류분을 정량하고 확인할 수 있는 새로운 분석법을 확립하고자 tandem HPLC(UV & FL) 및 APcI를 source로 사용한 LC/MS를 이용하였다. 이를 위해 FL(fluorescence) 검출기를 UV(ultraviolet) 검출기와 나란히 연결하여 UV 검출기의 경우 280 nm 파장을 그리고 FL 검출기의 경우는 excitation파장과 emission파장을 각각 280 mn와 310 nm로 설정하였다. 분석결과 carbendazim의 검출한계는 $0.04{\mu}g/kg$이었다. 콩나물에 carbendazim을 0.5, 1.0 및 2.0 ppm 수준으로 첨가하여 회수율을 측정한 결과 그 평균값은 89.1%이었다. APcI source를 사용한 LC/MS 질량스펙트럼 방법은 콩나물중 carbendazim 잔류분을 최종 확인할 수 있었다. APcI LC/MS 방법은 전자충격에 의한 질량스펙트럼에 비해 훨씬 간단한 fragment를 형성할 뿐 만 아니라 carbendazim의 경우 m/z 133, m/z 159, m/z 191($M^{+}$)의 전형적인 fragment 이온을 형성하므로, 이 방법을 병행한다면 콩나물중 carbendazim 잔류분을 효과적으로 확인할 수 있을 것으로 사료되었다.

• Korean Journal of Mathematics
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• 제4권2호
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• pp.83-88
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• 1996

In 1994 Z.Liang constructed an iterative method for the solution of nonlinear equations involving m-accretive operators in uniformly smooth Banach spaces. In this paper we apply the slight variants of Liang's iterative methods and generalize the results of Z.Liang. Moreover our proof is more simple than Liang's proof.

• Bulletin of the Korean Chemical Society
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• 제25권1호
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• pp.109-114
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• 2004

A sensitive method for quantitation of glimepiride in human plasma has been established using liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI/MS/MS). Glipizide was used as an internal standard. Glimepiride and internal standard in plasma sample was extracted using diethyl etherethyl acetate (1 : 1). A centrifuged upper layer was then evaporated and reconstituted with the mobile phase of acetonitrile-5 mM ammonium acetate (60:40, pH 3.0). The reconstituted samples were injected into a $C_{18}$ reversed-phase column. Using MS/MS in the multiple reaction monitoring (MRM) mode, glimepiride and glipizide were detected without severe interference from human plasma matrix. Glimepiride produced a protonated precursor ion ([M+H]$^+$) at m/z 491 and a corresponding product ion at m/z 352. And the internal standard produced a protonated precursor ion ([M+H]]$^+$) at m/z 446 and a corresponding product ion at m/z 321. Detection of glimepiride in human plasma by the LC-ESI/MS/MS method was accurate and precise with a quantitation limit of 0.1 ng/mL. The validation, reproducibility, stability, and recovery of the method were evaluated. The method has been successfully applied to pharmacokinetic studies of glimepiride in human plasma.

• Archives of Pharmacal Research
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• 제10권1호
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• pp.50-59
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• 1987

(E)-2-Phenylcyclopropylamine ((E)-TCP), (Z)-2-Phenylacyclopropylamine ((Z)-TCP), (E)-1-methyl-2-phenylcyclopropylamine ((E)-MTCP), and (Z)-1-methyl-2-phenylcyclopropylamine ((Z)-MTCP) were synthesized and used to determine to what extent 1-methylsubstitution and stereochemistry of 2-phenycyclopropylamines affect inhibition of monoamine oxidase (MAO). Inhibition of rat brain mitochondrial MAO-A and B by the compounds were measured using serotonin and benzylamine as the substrate, respectively and $IC_{50}$ values obtianed with 95% confidence limits by the method of computation. For the inhibition of MAO-A, (E)-MTPC ($IC_{50}$ = 6.2 * $10^{-8}$M) was found to be 37 times more potent than (Z)-MTCP ($IC_{50}$ = 7.8 * $10^{-8}$M), was 7 times more potent than (Z)-MTCP($IC_{50}$= 4.7 * $10^{-7}$M) and (E)-TCP($IC_{50}$ =7.8 * $10^{-8}$M),0.6 times as potent as (Z)- TCP ($IC_{50}$ = 4.4 * $10^{-8}$M). The results suggested that while without 1-methyl group, potency of a (Z)-isomer was comparable to that of (E)-isomer, the methyl group in its (Z)-position was very unfavorable to the inhibition of MAO and that in its (E)-position, the methyl group contributed positively to the potency as found by the fact that (E)-MTCP was 1-5 times more potent than (E)-TCP. In view of the selective inhibition of MAO-A- or B over MAO-A and 1-methyl substitution as well as the stereochemical factors did not significantly influence the selectivity.

• 한국축산식품학회지
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• 제34권6호
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• pp.749-756
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• 2014

A rapid and simple analytical method for L-carnitine was developed for infant and toddler formulas by liquid chromatography tandem mass spectrometry (LC-MS/MS). A 0.3 g of infant formula and toddler formula sample was mixed in a 50 mL conical tube with 9 mL water and 1 mL 0.1 M hydrochloric acid (HCl) to chemical extraction. Then, chloroform was used for removing a lipid fraction. After centrifuged, L-carnitine was separated and quantified using LC-MS/MS with electrospray ionization (ESI) mode. The precursor ion for L-carnitine was m/z 162, and product ions were m/z 103 (quantitative) and m/z 85 (qualitative), respectively. The results for spiked recovery test were in the range of 93.18-95.64% and the result for certified reference material (SRM 1849a) was within the range of the certificated values. This method could be implemented in many laboratories that require time and labor saving.

• 대한원격탐사학회지
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• 제24권5호
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• pp.483-496
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• 2008

Qualified ground control points (GCPs) are required to construct a digital elevation model (DEM) from a pushbroom stereo pair. An inverse geolocation algorithm for extracting GCPs from ERS SAR data and the SRTM DEM was recently developed. However, not all GCPs established by this method are accurate enough for direct application to the geometric correction of pushbroom images such as SPOT, IRS, etc, and thus a method for selecting and removing inaccurate points from the sets of GCPs is needed. In this study, we propose a method for evaluating GCP accuracy and winnowing sets of GCPs through orientation modeling of pushbroom image and validate performance of this method using SPOT stereo pair of Daejon City. It has been found that the statistical distribution of GCP positional errors is approximately Gaussian without bias, and that the residual errors estimated by orientation modeling have a linear relationship with the positional errors. Inaccurate GCPs have large positional errors and can be iteratively eliminated by thresholding the residual errors. Forty-one GCPs were initially extracted for the test, with mean the positional error values of 25.6m, 2.5m and -6.1m in the X-, Y- and Z-directions, respectively, and standard deviations of 62.4m, 37.6m and 15.0m. Twenty-one GCPs were eliminated by the proposed method, resulting in the standard deviations of the positional errors of the 20 final GCPs being reduced to 13.9m, 8.5m and 7.5m in the X-, Y- and Z-directions, respectively. Orientation modeling of the SPOT stereo pair was performed using the 20 GCPs, and the model was checked against 15 map-based points. The root mean square errors (RMSEs) of the model were 10.4m, 7.1m and 12.1m in X-, Y- and Z-directions, respectively. A SPOT DEM with a 20m ground resolution was successfully constructed using a automatic matching procedure.

• 한국환경과학회지
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• 제31권2호
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• pp.171-180
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• 2022

Zeolitic material, Z-Y3, was synthesized from coal fly ash (CFA) under low-alkaline conditions (NaOH/CFA ratio = 0.3 and NaOH solution concentrations of 0.0, 0.5, and 1.0 M) using a fusion/hydrothermal method. The adsorption capacities of the fabricated Z-Y3 samples for Cs and Sr ions and the desorption capacity of Na ions were evaluated. The XRD patterns of the Z-Y3 sample fabricated using a 1.0 M NaOH solution (Z-Y3 (1.0 M)) indicated the successful synthesis of a zeolitic material, because the diffraction peaks of Z-Y3 coincided with those of the Na-A zeolite in the 2θ range of 7.18-34.18. Moreover, the SEM images revealed that morphology of the Z-Y3 (1.0 M) sample, which presented zeolitic materials characteristics, consisted of sharp-edged cubes. The adsorption isotherms of Cs and Sr ions on all the fabricated Z-Y3 samples were described using the Langmuir model, and the maximum adsorption capacities of Cs and Sr were calculated to be 0.14-0.94 mmol/g and 0.19-0.78 mmol/g, respectively. The desorption of Na ions from the Cs and Sr ions adsorbed Z-Y3 samples followed the Langmuir desorption model. The maximum desorption capacities of Na ions from the Cs and Sr ions adsorbed Z-Y3 (1.0 M) samples were 1.28 and 1.49 mmol/g, respectively.