• 한국실내디자인학회논문집
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• 제19권1호
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• pp.180-189
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• 2010

Since collective houses are started to be supplied, the housing market has been transformed from supplier to demander oriented, and various type with same area of unit households have been deigned and started to be distributed. It can be expected that such transfer phenomenon would be continuously sped-up, and unit household will be more subdivided and varied. Thus, we analysed and studied the planes with subject of unit households in national housing scale ($85m^2$) that is treated as supply standard and has biggest volume in construction by Korean housing corporation. The analysing method is investigating the area of each room within unit household, calculating their minimum, maximum, and average values, studying the efficiency of unit household plane according to the structure of each room by comparative analysis these values, and analysing changing matter by investigating any change of each room area. The analysing results of which are followings. At first, number of BAY on face is increasing. Second, allocation of each room has been vary. Third, area ratio among bedroom1, livingroom, diningroom/kitchen become similar. Fourth, the area of diningroom/kitchen become somewhat bigger. Fifth, the space for passage way is efficiently allocated. Sixth, service area is reduced, Seventh, stereotyped phenomenon Is appeared. Based on many studies so far, any improvements of unit householder in national housing scale are followings. First, in terms of forming style, unit householder in national housing scale is unfolded in various way though, the form of each room is not more than typical style. Second, it shows stereotyped phenomenon. Especially, bathroom 1, 2 show stereotyped feature in terms of their type and area across entire research years, also LDK allocation method is stereotyped, as well as stereotyped trend in bedroom 2, 3, allocation for 4 BAY type.

• 한국정보통신학회논문지
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• 제17권1호
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• pp.190-196
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• 2013

커브형 집적 영상 기술은 렌즈 배열을 이용하여 3D 영상을 공간에 쉽게 표현할 수 있는 기술이며, 넓은 관측각을 제공한다. 본 논문에서는 커브형 집적 영상에서 물체의 인식 향상을 위하여 다이렉트 픽셀 매핑 (DPM) 방법 기반의 비선형 상관기를 제안한다. 제안하는 비선형 상관기는 커브형 집적 영상 시스템에서 장애물에 가려진 물체로부터 픽업된 요소 영상을 DPM 방법을 통하여 해상도가 향상된 새로운 요소 영상을 생성한다. 새로운 생성된 요소 영상을 사용하여 복원한 3D 영상들과 참조 영상간의 비선형 상호상관을 이용하여 3D 물체의 인식 성능 향상시킨다. 제안된 방법의 유용함을 보이기 위하여 기초적인 상관 관계 실험을 수행하고 기존의 방법과의 비교 결과를 보고한다.

• 터널과지하공간
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• 제8권4호
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• pp.296-306
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• 1998

바쿤 수력발전 공사계획은 대형댐과 2,520 MW 출력량의 수력발전소를 건설하는 대형 턴키 프로젝트이며 현재는 발전댐 건설에 앞서 3개의 가베수 터널이 시공중에 있다. 바쿤 지역은 유기물 함량이 높아 쉽게 부서지는 퇴적지층으로 이러한 열대우림지역에서 가배수로 터널의 지보설계를 위해 전체적인 암층단위를 공학적인 목적과 역학적 거동양상을 토대로 주도적인 암종에 따라 분류하였다. 또한 이러한 암층단위를 기준으로 풍화정도와 절리의 빈도 및 특성을 고려하여 다시 4개의 암반유형으로 분류하였고 또한 가배수로 터널의 특성과 현재의 지반특성과 현재의 지반특성을 고려하여 지반내 swelling 광물의 존재를 확인하였다. 다양한 암반과 지보조건에 적합한 다양한 Swellex 록볼트를 적용하였으며 지지력이 낮은 록볼트를 사용할 대 발생되는 문제는 볼트의 면적에 따른 록볼트의 양을 조절하여 해결하였다. 또한 계측결과와 전산해석 결과에 따라 지보재의 설치간격, 수량을 조절하였으며, 계측결과에 따른 역해석을 실시하여 최적의 지보패턴을 결정하였다.

• 터널과지하공간
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• 제23권3호
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• pp.228-240
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• 2013

퇴적암에서 나타나는 이방성은 층리에 의한 영향이 크며, 암석의 수리적 특성에도 영향을 주게 된다. 본 연구에서는 층리가 발달한 다공질 사암을 대상으로, 층리구조에 의해 발생한 공극구조 이방성이 사암의 수리 이방성에 미치는 영향을 분석하였다. 사암의 공극구조 이방성 파악을 위해 X-ray CT(computed tomography)를 이용하여 내부 공극률의 변화양상을 분석하였다. 층리방향에 따른 수리이방성은 층리면과 수평면이 이루는 각도를 $0^{\circ}$에서 $90^{\circ}$까지 $15^{\circ}$간격으로 코어링한 샘플을 제작하여 투수실험을 통해 파악하였다. 투수실험 결과 층리면과 투수방향이 수직인 경우 투수율이 가장 작은 값을 나타낸 반면, 층리면과 투수방향이 평행일 때 가장 높은 투수율을 나타내었으며, 평균 수리이등방비($k_{90^{\circ}}/k_{0^{\circ}}$)가 1.8로 층리에 따른 수리 이방성이 확연하게 나타났다. 또한, 이러한 사암의 수리이방특성은 층리에 의해 공극특성이 서로 다른 층상구조가 형성되기 때문임을 확인하였다.

• 한국항행학회논문지
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• 제17권5호
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• pp.491-496
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• 2013

본 논문에서는 보안등의 통합 모니터링과 제어를 위한 3G 이동통신용 RF모듈에 적용 가능한 반파장 폴디드 슬롯 안테나를 제안하였다. 제안된 안테나는 입력임피던스가 $50{\Omega}$에 가까운 총 길이가 ${\lambda}g$인 전형적인 폴디드 슬롯 안테나의 장점을 유지하면서 절반의 크기를 가지고 PCB의 가장자리에 위치할 수 있도록 변형된 폴디드 슬롯 구조이다. 제안된 안테나는 국내 3G 이동통신 대역용으로, $40.5{\times}62mm^2$의 기판 중 상단 $40.5{\times}10mm^2$의 공간을 이용하여 설계 및 제작하였다. 제작된 안테나를 측정한 결과, 390 MHz의 대역폭, 2 dBi의 이득을 얻을 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제14권1호
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• pp.82-86
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• 1993

Two crystal structures of dehydrated $Ag_{3.3}Ca_{4.35}-A ({\alpha} = 12.256(2){\AA})$ and of its ethylene sorption complex (${\alpha} = 12.259(2){\AA}$) have been determined by single-crystal X-ray diffraction techniques in the cubic space group Pm3m at 21(l)$^{\circ}$C. Both crystals were dehydrated at 360$^{\circ}$C and $2{\times}10^{-6}$ Torr for 2 days and one crystal was treated with 200 Torr of ethylene at 24(2)$^{\circ}$C. The structures were refined to final error indices, $R_1$=O.065 and $R_2$ = 0.088 with 202 reflections and $R_1$=0.049 and $R_2$ = 0.044 with 259 reflections, respectively, for which I>3${\sigma}$(I). In these structures, all Ag$^+$ and Ca$^{2+}$ ions are located on two and three different threefold axes associated with 6-ring oxygens, respectively. In $Ag_{3.3}Ca_{4.35}-A{\cdot}6.65\;C_2H_4,\;3.3\;Ag^+\;and\;3.35\;Ca^{2+}$ ions are recessed 1.09 ${\AA}$ and 0.21 ${\AA}$, respectively, into the large cavity from the (111) plane at O(3). Each Ag$^+$ and Ca$^{2+}$ ion in the large cavity forms a complex with one $C_2H_4$$^{2+}$ ions and ethylene molecules are longer than those between Ag$^+$ ions and ethylene molecules.

• Bulletin of the Korean Chemical Society
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• 제14권1호
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• pp.137-143
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• 1993

The tetranuclear heterometallic complex CpMo$Os_3(CO)_{10}({\mu]-H)2[{\mu}3-{\eta}^2-C(O)CH_2Tol]\;(1,\;Cp={\eta}^5-C_5H_5,\;Tol=p-C_6H_4Me)$ has been examined by variable-temperature $^{13}$C-NMR spectroscopy and by a full three-dimensional X-ray structual analysis. Complex 1 crystallizes in the orthorhombic space group Pna2$_1$ with a = 12.960(1) ${\AA}$, b = 11.255(l) ${\AA}$, c = 38.569(10)${\AA}$, V = 5626(2) ${\AA}^3$ and ${\rho}$(calcd) = 2.71 gcm$^{-3}$ for Z = 8 and molecular weight 1146.9. Diffraction data were collectedon a CAD4 diffractometer, and the structure was refined to $R_F$ = 9.7% and $R_{W^F}$ = 9.9% for 2530 data (MoK${\alpha}$ radiation). There are two essentially equivalent molecules in the crystallographic asymmetric unit. The tetranuclear molecule contains a triangulated rhomboidal arrangement of metal atoms with Os(2) and Mo at the two bridgehead positions. The metal framework is planar; the dihedral angle between Os(l)-Os(2)-Mo and Os(3)-Os(2)-Mo planes is 180$^{\circ}$. A triply bridging (${\mu}_3,\;{\eta}^2$) acyl ligand lies above the Os(l)-Os(2)-Mo plane; the oxygen atom spans the two bridgehead positions, while the carbon atom spans one bridgehead position and an acute apical position. The molecular architecture is completed by an ${\eta}^5$-cyclopentadienyl ligand and a semi-triply bridging carbonyl ligand on the molybdenum atom, and nine terminal carbonyl ligands-four on Os(3), three on Os(l), and two on Os(2). The two hydride ligands are inferred to occupy the Os(l)-Os(2) and Mo-Os(3) edges from structural and NMR data.

• 대한원격탐사학회지
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• 제18권1호
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• pp.53-59
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• 2002

The MSC is a payload on the KOMPSAT-2 satellite to perform the earth remote sensing. The instrument images the earth using a push-broom motion with a swath width of 15 km and a GSD(Ground Sample Distance) of 1 m over the entire FOV(Field Of View) at altitude 685 km. The instrument is designed to haute an on-orbit operation duty cycle of 20% over the mission lifetime of 3 years with the functions of programmable gain/offset and on-board image data compression/storage. The MSC instrument has one channel for panchromatic imaging and four channel for multi-spectral imaging covering the spectral range from 450nm to 900nm using TDI(Time Belayed Integration) CCD(Charge Coupled Device) FPA(Focal Plane Assembly). The MSC hardware consists of three subsystem, EOS(Electro Optic camera Subsystem), PMU(Payload Management Unit) and PDTS(Payload Data Transmission Subsystem) and each subsystems are currently under development and will be integrated and verified through functional and space environment tests. Final verified MSC will be delivered to spacecraft bus for AIT(Assembly, Integration and Test) and then COMSAT-2 satellite will be launched after verification process through IST(Integrated Satellite Test). In this paper, the introduction of MSC, the configuration of MSC electronics including electrical interlace and design of CEU(Camera Electronic Unit) in EOS are described. MSC Operation parameters induced from the operation concept are discussed and analyzed to find the influence of system for on-orbit operation in future.

• Bulletin of the Korean Chemical Society
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• 제16권9호
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• pp.823-826
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• 1995

The crystal structure of a sulfur sorption complex of the dehydrated partially Co2+ exchanged zeolite A (a=12.058(2) Å) has been determined by single-crystal X-ray techniques. The crystal structure was solved and refined in cubic space group Pm3m at 21(1) ℃. Ion Exchange with aqueous 0.05 M Co(NO3)2 was done by the static method. The crystal of Na4Co4-A was dehydrated at 380 ℃ and 2 × 10-6 Torr for 2 days, followed by exposure to about 100 Torr of sulfur at 330 ℃ for 72 h. Full matrix least-squares refinement converged to R1=0.084 and Rw=0.074 with 102 reflections for which I > 3σ(I). Crystallographic analysis shows that 2.8 Co2+ ions and 4 Na+ ions per unit cell occupy 6-ring sites on the threefold axes. 1.2 Co2+ ions occupy the 8-ring sites on fourfold axes. 2.8 Co2+ ions at Co(1) are recessed 0.66 Å into the large cavity and 4 Na+ ion at Na(1) are recessed 0.77 Å into the sodalite cavity from the (111) plane of O(3)'s. Approximately 16 sulfur atoms were sorbed per unit cell. Two S8 rings, each in a butterfly form, are found in the large cavity. The bond length between S and its adjacent S is 2.27(3) Å. The distance between 6-ring Co2+ ion and its adjacent sulfur is 2.53 (2) Å and that between 8-ring Co2+ ions and its adjacent sulfur is 2.72(9) Å. The angles of S-S'-S and S'-S-S'/ in octasulfur rings are 119.0(2)°and 113.0(2)°, respectively.

• Bulletin of the Korean Chemical Society
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• 제10권5호
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• pp.426-430
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• 1989

Two crystal structures of iodine sorption complexes of dehydrated partially Co(Ⅱ )-exchanged zeolite A, $Co_{3.5}Na_5-A{\cdot}xI_2$, x = 2.5 and 5.0, have been determined by single crystal X-ray diffraction techniques. Both structures were solved and refined in cubic space group, Pm3m at $21(1)^{\circ}C$. The structures of $Co_{3.5}Na_5-A{\cdot}2.5I_2$(a = 12.173(1) ${\AA}$) and $Co_{3.5}Na_5-A{\cdot}5.0I_2$(a = 12.130(1) ${\AA}$) were refined to the final error indices, $R_1$ = 0.081 and $R_2$ = 0.077 with 261 reflections and $R_1$ = 0.103 and $R_2$ = 0.112 with 225 reflections, respectively, for which I>3${\sigma}$(I). In both structures, 3.5 $Co^{2+}$ ions and 4.5 $Na^+$ ions per unit cell lie at two crystallographically different 6-ring positions. 0.5 $Na^+$ ion lines in an 8-oxygen ring plane. Dehydrated $Co_{3.5}Na_5$-A sorbs 2.5 iodine molecules per unit cell at $70^{\circ}C$ (vapor pressure of $I_2$ is ca. 8.3 torr) within 30 minutes and 5 iodine molecules per unit cell at $80^{\circ}C$ (vapor pressure of $I_2$ is ca. 14.3 torr) within 24 hours. Each iodine molecule makes a close approach, along its axis to framework oxygen atom with I-I-O = $175^{\circ}$.