• 한국자기학회지
• /
• 제6권4호
• /
• pp.264-271
• /
• 1996

본 연구에서는 SQUID를 이용한 생체자기 계측연구에 사용될 자기차폐실의 설치 및 차폐 특성에 대해 소개한다. 차폐실 내부공간의 크기는 $2m(길이){\times}2m(폭){\times}2.5m(높이)$이고 차폐재료는 높은 투자율을 가진 Mumetal과 전기 전도도가 높은 알루미늄으로 구성되어 있다. 직류 지구자장에 대한 차폐율은 차폐실 중심에서 60 dB 이상이며 교류자장에 대한 차폐율은 1 Hz에서는 60 dB, 10 Hz에서는 80~100 dB의 값을 가진다. 차폐실내에서의 자장 잡음은 1 Hz에서 $500\;fT/{\sqrt}Hz$, 10 Hz에서 $100\;fT/{\sqrt}Hz$의 값을 가지며 자장구배잡음은 1 Hz에서 $7\;fT/cm{\sqrt}Hz$ 이하로서 SQUID 자력계에 의한 심자도와 SQUID gradiometer에 의한 뇌자도측정이 가능한 수준이다. 자체 개발된 SQUID 센서를 이용하여 차폐실내에서 심장 및 노로부터 발생하는 자기신호를 검출하였다.

• 아시안잔디학회지
• /
• 제10권1호
• /
• pp.31-40
• /
• 1996

The mechanical expresion provides for the use of Soil property reserves and permanent protec-tion or improvement of soil resources in accordance with measurable standards. If the functions I (initial soil property), E (soil erosion), R (soil renewal), and M. (minimum allowable value) are assumed to be integrable in region A, erosion tolerance over a region is leaded to ${\int}_A{\int}I(m, cl, re, ch, b)dA-{\int}_A{\int}{\{\int}_{to}^{\infty}[E(w, re, c, re, ch, b, t)-R(m, ch, re, b, t)]dt}\dA{\geqq}{\int}_A{\int}M_i(m, cl, re, ch, b)dA$ were variable factors are m=parent material of soil, cl=climate, re=relief or topography, ch=soil characteristics, r=rain or water, w=wind, b=biota, and t=time.

• 마이크로전자및패키징학회지
• /
• 제8권4호
• /
• pp.17-23
• /
• 2001

3차원 홀 센서는 두 개의 수평 자계($\chi$, y성분) 검출부와 한 개의 수직 자계(z 성분) 검출부를 갖는다. 종래의 3차원 홀 센서는 일반적으로 $B_{z}$에 대한 감도가 $B_\chi, B_y$에 대한 감도의 약 1/10정도에 그친다. 본 연구에서는 새로운 구조를 갖는 3차원 홀 센서를 제안하였다. 이방성 식각을 이용하여 트랜치를 형성함으로써 감도를 약 6배 증가시켰다. 또한 자속을 집속시키기 위하여 웨이퍼 후면에 강자성체 박막을 증가시킴으로써 $B_{z}$에 대한 감도를 $B_\chi, B_y$에 대한 감도의 약 80% 정도로 증가시켰다. 전류 3 mA를 인가했을 때, Ni/Fe 박막을 증착하여 제작된 센서의 감도는 $B_\chi, B_y$, B$_{z}$ 에 대하여 각각 120.1 mV/T, 111.7 mV/T, 그리고 95.3 mV/T로 측정되었다. 센서의 선형성을 오차가 $\pm$3%로 우수하였다.

• 대한핵의학회:학술대회논문집
• /
• 대한핵의학회 1990년도 제29차 춘계학술대회
• /
• pp.193.1-193.1
• /
• 1990

• 대한핵의학회:학술대회논문집
• /
• 대한핵의학회 1989년도 제28차 춘계학술대회
• /
• pp.137.2-137.2
• /
• 1989

• 한국응용과학기술학회지
• /
• 제18권3호
• /
• pp.214-232
• /
• 2001

CTA ester bonds in TG molecules were not attacked by pancreatic lipase and lipases produced by microbes such as Candida cylindracea, Chromobacterium viscosum, Geotricum candidium, Pseudomonas fluorescens, Rhizophus delemar, R. arrhizus and Mucor miehei. An aliquot of total TG of all the seed oils and each TG fraction of the oils collected from HPLC runs were deuterated prior to partial hydrolysis with Grignard reagent, because CTA molecule was destroyed with treatment of Grignard reagent. Deuterated TG (dTG) was hydrolyzed partially to a mixture of deuterated diacylglycerols (dDG), which were subsequently reacted with (S)-(+)-1-(1-naphthyl)ethyl isocyanate to derivatize into dDG-NEUs. Purified dDG-NEUs were resolved into 1, 3-, 1, 2- and 2, 3-dDG-NEU on silica columns in tandem of HPLC using a solvent of 0.4% propan-1-o1 (containing 2% water)-hexane. An aliquot of each dDG-NEU fraction was hydrolyzed and (fatty acid-PFB ester). These derivatives showed a diagnostic carboxylate ion, $(M-1)^{-}$, as parent peak and a minor peak at m/z 196 $(PFB-CH_{3})^{-}$ on NICI mass spectra. In the mass spectra of the fatty acid-PFB esters of dTGs derived from the seed oils of T. kilirowii and M. charantia, peaks at m/z 285, 287, 289 and 317 were observed, which corresponded to $(M-1)^{-}$ of deuterized oleic acid ($d_{2}-C_{18:0}$), linoleic acid ($d_{4}-C_{18:0}$), punicic acid ($d_{6}-C_{18:0}$) and eicosamonoenoic acid ($d_{2}-C_{20:0}$), respectively. Fatty acid compositions of deuterized total TG of each oil measured by relative intensities of $(M-1)^-$ ion peaks were similar with those of intact TG of the oils by GLC. The composition of fatty acid-PFB esters of total dTG derived from the seed oils of T. kilirowii are as follows; $C_{16:0}$, 4.6 mole % (4.8 mole %, intact TG by GLC), $C_{18:0}$, 3.0 mole % (3.1 mole %), $d_{2}C_{18:0}$, 11.9 mole % (12.5 mole %, sum of $C_{18:1{\omega}9}$ and $C_{18:1{\omega}7}$), $d_{4}-C_{18:0}$, 39.3 mole % (38.9 mole %, sum of $C_{18:2{\omega}6}$ and its isomer), $d_{6}-C_{18:0}$, 41.1 mole % (40.5 mole %, sum of $C_{18:3\;9c,11t,13c}$, $C_{18:3\;9c,11t,13r}$ and $C_{18:3\;9t,11t,13c}$), $d_{2}-C_{20:0}$, 0.1 mole % (0.2 mole % of $C_{20:1{\omega}9}$). In total dTG derived from the seed oils of M. charantia, the fatty acid components are $C_{16:0}$, 1.5 mole % (1.8 mole %, intact TG by GLC), $C_{18:0}$, 12.0 mole % (12.3 mole %), $d_{2}-C_{18:0}$, 16.9 mole % (17.4 mole %, sum of $C_{18:1{\omega}9}$), $d_{4}-C_{18:0}$, 11.0 mole % (10.6 mole %, sum of $C_{18:2{\omega}6}$), $d_{6}-C_{18:0}$, 58.6 mole % (57.5 mole %, sum of $C_{18:3\;9c,11t,13t}$ and $C_{18:3\;9c,11t,13c}$). In the case of Aleurites fordii, $C_{16:0}$; 2.2 mole % (2.4 mole %, intact TG by GLC), $C_{18:0}$; 1.7 mole % (1.7 mole %), $d_{2}-C_{18:0}$; 5.5 mole % (5.4 mole %, sum of $C_{18:1{\omega}9}$), $d_{4}-C_{18:0}$ ; 8.3 mole % (8.5 mole %, sum of $C_{18:2{\omega}6}$), $d_{6}-C_{18:0}$; 82.0 mole % (81.2 mole %, sum of $C_{18:3\;9c,11t,13t}$ and $C_{18:3 9c,11t,13c})$. In the stereospecific analysis of fatty acid distribution in the TG species of the seed oils of T. kilirowii, $C_{18:3\;9c,11t,13r}$ and $C_{18:2{\omega}6}$ were mainly located at sn-2 and sn-3 position, while saturated acids were usually present at sn-1 position. And the major molecular species of $(C_{18:2{\omega}6})(C_{18:3\;9c,11t,13c})_{2}$ and $(C_{18:1{\omega}9})(C_{18:2{\omega}6})(C_{18:3\;9c,11t,13c})$ were predominantly composed of the stereoisomer of $sn-1-C_{18:2{\omega}6}$, $sn-2-C_{18:3\;9c,11t,13c}$, $sn-3-C_{18:3\;9c,11t,13c}$, and $sn-1-C_{18:1{\omega}9}$, $sn-2-C_{18:2{\omega}6}$, $sn-3-C_{18:3\;9c,11t,13c}$, respectively, and the minor TG species of $(C_{18:2{\omega}6})_{2}(C_{18:3\;9c,11t,13c})$ and $ (C_{16:0})(C_{18:3\;9c,11t,13c})_{2}$ mainly comprised the stereoisomer of $sn-1-C_{18:2{\omega}6}$, $sn-2-C_{18:2{\omega}6}$, $sn-3-C_{18:3\;9c,11t,13c}$ and $sn-1-C_{16:0}$, $sn-2-C_{18:3\;9c,11t,13c}$, $sn-3-C_{18:3\;9c,11t,13c}$. The TG of the seed oils of Momordica charantia showed that most of CTA, $C_{18:3\;9c,11t,13r}$, occurred at sn-3 position, and $C_{18:2{\omega}6}$ was concentrated at sn-1 and sn-2 compared to sn-3. Main TG species of $(C_{18:1{\omega}9})(C_{18:3\;9c,11t,13t})_{2}$ and $(C_{18:0})(C_{18:3\;9c,11t,13t})_{2}$ were consisted of the stereoisomer of $sn-1-C_{18:1{\omega}9}$, $sn-2-C_{18:3\;9c,11t,13t}$, $sn-3-C_{18:3\;9c,11t,13t}$ and $sn-1-C_{18:0}$, $sn-2-C_{18:3\;9c,11t,13t}$, $sn-3-C_{18:3\;9c,11t,13t}$, respectively, and minor TG species of $(C_{18:2{\omega}6})(C_{18:3\;9c,11t,13c})_{2}$ and $(C_{18:1{\omega}9})(C_{18:2{\omega}6})(C_{18:3\;9c,11t,13c})$ contained mostly $sn-1-C_{18:2{\omega6}$, $sn-2-C_{18:3\;9c,11t,13t}$, $sn-3-C_{18:3\;9c,11t,13t}$ and $sn-1-C_{18:1{\omega}9}$, $sn-2-C_{18:2{\omega}6}$, $sn-3-C_{18:3\;9c,11t,13t}$. The TG fraction of the seed oils of Aleurites fordii was mostly occupied with simple TG species of $(C_{18:3\;9c,11t,13t})_{3}$, along with minor species of $(C_{18:2{\omega}6})(C_{18:3\;9c,11t,13t})_{2}$, $(C_{18:1{\omega}9})(C_{18:3\;9c,11t,13t})_{2}$ and $(C_{16:0})(C_{18:3\;9c,11t,13t})$. The sterospecific species of $sn-1-C_{18:2{\omega}6}$, $sn-2-C_{18:3\;9c,11t,13t}$, sn-3-C_{18:3\;9c,11t,13t}$, $sn-1-C_{18:1{\omega}9}$, $sn-2-C_{18:3\;9c,11t,13t}$, $sn-3-C_{18:3\;9c,11t,13t}$ and $sn-1-C_{16;0}$, $sn-2-C_{18:3\;9c,11t,13t}$, $sn-3-C_{18:3\;9c,11t,13t}$ are the main stereoisomers for the species of $(C_{18:2{\omega}6})(C_{18:3\;9c,11t,13t})_2$, $(C_{18:1{\omega}9})(C_{18:3\;9c,11t,13t})_{2}$ and $(C_{16:0})(C_{18:3\;9c,11t,13t})$, respectively.

• 한국생물공학회:학술대회논문집
• /
• 한국생물공학회 2001년도 추계학술발표대회
• /
• pp.646-647
• /
• 2001

The enzymatic synthesis of conjugates of lysine and aspartic acid with D-glucose was studied. Optimase M-440 showed the very poor regioselectivity in the transesterification of $N{\alpha}$,$N'{\varepsilon}-di-t-Boc-L-Lys-OTFE$ and N-t-Boc-L-Asp-diOTFE with D-glucose. The acylation of glycosidic -OH and primary -OH of D-glucose occurred. However, Optimase M-440 catalyzed only the acylation of primary -OH group in the transesterification of $N{\alpha}$,$N'{\varepsilon}-di-t-Boc-L-Lys-OTFE$ and N-t-Boc-L-Asp-diOTFE with ${\alpha}-$ and ${\beta}-methylglucopyranoside$ in high yields without any other transesterification. Optimase M-440 also discriminated carboxyl groups of N-t-Boc-L-Asp-diOTFE.

• 대한수학회보
• /
• 제47권3호
• /
• pp.551-561
• /
• 2010

In this paper we give a new characterization of real hypersurfaces of type B, that is, a tube over a totally geodesic $\mathbb{Q}P^n$ in complex two-plane Grassmannians $G_2(\mathbb{C}^{m+2})$, where m = 2n, with the Reeb vector $\xi$ belonging to the distribution $\mathfrak{D}$, where $\mathfrak{D}$ denotes a subdistribution in the tangent space $T_xM$ such that $T_xM$ = $\mathfrak{D}{\bigoplus}\mathfrak{D}^{\bot}$ for any point $x{\in}M$ and $\mathfrak{D}^{\bot}=Span{\xi_1,\;\xi_2,\;\xi_3}$.

• 한국자기학회지
• /
• 제10권3호
• /
• pp.99-105
• /
• 2000

두 종류의 유전체 층(A: $SiO_2$, B: T $a_2$ $O_{5}$ )을 주기적으로 적층한 구조에, Bi를 다량 치환한 가네트 박막(M: $Y_{1.93}$ B $i_{1.07}$F $e_{5}$ $O_{12}$ )을 결함층으로 삽입한 (A/B)$^{k}$ /M(B/A)$^{k}$ 의 구조를 갖는 1차원 자성 포토닉 결정의 자기 광학 특성을 수치해석하였다. 가시광과 적외선 영역에서 1차원 자성 포토닉 결정의 자성체 층의 두께( $d_{M}$)와 유전체 층의 적층수(k)를 변화시키며, 투과율(T)과 페러데이 회전각($\theta$$_{F}$ ) 및 성능지수(Q)를 조사하였다. 조사한 1차원 자성 포토닉 결정의 각 국재 모드에서의 페러데이 회전각 및 성능지수의 극대값들은 동일 조성의 단층 가네트 박막에 비해 수 배 내지 수 백 배 큰 값이 얻어졌다. 가시광 영역에서는 k = 11이고, $d_{M}$ = 375 nm일때, 최대값 Q = 0.15이 얻어졌다. 이 값은 단층의 가네트 막에 비해 약 30배 큰 값이며, 이 때의 = 720 nm, T = 0.54, $\theta$ = 8.13$^{\circ}$이었다. 적외선 영역에서는 k = 11이고, $d_{M}$ = 800 nm일때 , 최대값 Q = 0.285(단층 가네트 막에 비해 100배 큰 값)이 얻어졌고, 이 때의 = 1114 nm, T = 0.485, $\theta$$_{F}$ = 18$^{\circ}$이었다.

• E2M - 전기 전자와 첨단 소재
• /
• 제16권1호
• /
• pp.63.2-63
• /
• 2003