(Na, K) NbO3 thick film was successfully achieved using a sol-gel coating process with the addition of polyvinylpyrrolidone (PVP) to a metal alkoxide solution. The transparent coating solution, mixed with Nb:PVP = 1:1 in a molar ration, was synthesized by evaporating the solvent to over 62.5 wt%. Additive PVP increased the viscosity of the solution so that the coating thickness could be enhanced. The thickness of the (Na, K) NbO3 film assisted by PVP was ca. 320 nm at the time of deposition; this value is four times thicker than that of the sample fabricated without PVP. Also, due to PVP binding with the OH groups of the metal alkoxide, the condensation reaction in the film was suppressed. The crystalline size of the (Na, K) NbO3 films assisted by PVP was ca. 15 nm smaller than that of the film fabricated without PVP. After the sintering process at 700˚C, the (Na, K) NbO3 films were mainly composed of randomly oriented (Na, K) NbO3 phase of perovskite crystal structure, including a somewhat secondary phase of K2Nb4O11. However, by adding PVP, the content of the secondary phase became quite smaller than that of the sample without PVP. It was thought that the addition of PVP might have the effect of restraining the loss of potassium and that PVP could hold metalloxane by strong hydrogen bonding before complete decomposition. Therefore, the film thickness of the (Na, K) NbO3 films could be considerably advanced and made more crack-free by the addition of PVP.

We have examined the co-doping effects of 1/2mol% NiO and 1/4mol% Cr2O3 (Ni:Cr=1:1) on the reaction,microstructure, and electrical properties, such as the bulk defects and the grain boundary properties, of ZnO-Bi2O3-Sb2O3 (ZBS;Sb/Bi=0.5, 1.0, and 2.0) varistors. The sintering and electrical properties of Ni,Cr-doped ZBS, ZBS(NiCr) varistors werecontrolled using the Sb/Bi ratio. Pyrochlore (Zn2Bi3Sb3O14), α-spinel (Zn7Sb2O12), and δ-Bi2O3 were detected for all ofcompositions. For the sample with Sb/Bi=1.0, the Pyrochlore was decomposed and promoted densification at lowertemperature by Ni rather than by Cr. A homogeneous microstructure was obtained for all of the samples affected by α-spinel.The varistor characteristics were not dramatically improved (non-linear coefficient, α=5~24), and seemed to formZni..(0.17eV) and Vo.(0.33eV) as dominant defects. From impedance and modulus spectroscopy, the grain boundaries werefound to have been divided into two types, i.e., one is tentatively assigned to ZnO/Bi2O3 (Ni,Cr)/ZnO (0.98eV) and the otheris assigned to a ZnO/ZnO (~1.5eV) homojunction.

In this study we aimed to examine the co-doping effects of 1/6mol% Co3O4 and 1/4mol% Cr2O3 (Co:Cr=1:1)on the reaction, microstructure, and electrical properties, such as the bulk defects and the grain boundary properties, of ZnO-Bi2O3-Sb2O3 (ZBS; Sb/Bi=0.5, 1.0, and 2.0) varistors. The sintering and electrical properties of Co,Cr-doped ZBS, ZBS(CoCr)varistors were controlled using the Sb/Bi ratio. Pyrochlore (Zn2Bi3Sb3O14), α-spinel (Zn7Sb2O12), and δ-Bi2O3 were formed inall systems. Pyrochlore was decomposed and promoted densification at lower temperature on heating in Sb/Bi=1.0 by Cr ratherthan Co. A more homogeneous microstructure was obtained in all systems affected by α-spinel. In ZBS(CoCr), the varistorcharacteristics were improved (non-linear coefficient, α=20~63), and seemed to form Zni..(0.20eV) and Vo.(0.33eV) asdominant defects. From impedance and modulus spectroscopy, the grain boundaries were found to be composed of anelectrically single barrier (0.94~1.1eV) that is, however, somewhat sensitive to ambient oxygen with temperature. The phasedevelopment, densification, and microstructure were controlled by Cr rather than by Co but the electrical and grain boundaryproperties were controlled by Co rather than by Cr.

We aimed to examine the co-doping effects of 1/6mol% Mn3O4 and 1/4mol% Cr2O3 (Mn:Cr=1:1) on the reaction,microstructure, and electrical properties, such as the bulk defects and grain boundary properties, of ZnO-Bi2O3-Sb2O3 (ZBS;Sb/Bi=0.5, 1.0, and 2.0) varistors. The sintering and electrical properties of Mn,Cr-doped ZBS, ZBS(MnCr) varistors werecontrolled using the Sb/Bi ratio. Pyrochlore (Zn2Bi3Sb3O14), α-spinel (Zn7Sb2O12), and δ-Bi2O3 (also β-Bi2O3 at Sb/Bi≤1.0)were detected for all of the systems. Mn and Cr are involved in the development of each phase. Pyrochlore was decomposedand promoted densification at lower temperature on heating in Sb/Bi=1.0 system by Mn rather than Cr doping. A morehomogeneous microstructure was obtained in all systems affected by α-spinel. In ZBS(MnCr), the varistor characteristics wereimproved dramatically (non-linear coefficient, α=40~78), and seemed to form Vo.(0.33eV) as a dominant defect. Fromimpedance and modulus spectroscopy, the grain boundaries can be seen to have divided into two types, i.e. one is tentativelyassigned to ZnO/Bi2O3 (Mn,Cr)/ZnO (0.64~1.1eV) and the other is assigned to the ZnO/ZnO (1.0~1.3eV) homojunction.

Yellow phosphor dispersed color conversion glasses are promising phosphor materials for white LED applications because of their good thermal durability, chemical stability, and anti-ultraviolet property. Six color conversion glasses were prepared with high Tg and low Tg specimens of glass. Luminous efficacy, luminance, CIE (Commission Internationale de l'Eclairage) chromaticity, CCT (Correlated Color Temperature), and CRI (Color Rendering Index) of the color conversion glasses were analyzed according to the PL spectrum. Color conversion glasses with high Tg glass frit, sintered at higher temperature, showed better luminous properties than did color conversion glasses with low Tg glass frit. The characteristics of the color conversion glass depended on the glass composition rather than on the sintering temperature. The XRD peaks of the YAG phosphor disappeared in the color conversion glass with major components of B2O3-ZnO-SiO2-CaO and, in the XRD results, new crystalline peaks of BaSi2O5 appeared in the color conversion glass with major components of Bi2O3-ZnO-B2O3-MgO. The characteristics of CIE chromaticity, CCT, and the CRI of low Tg color conversion glasses showed worse color properties than those of high Tg color conversion glasses. However, these color characteristics of low Tg glasses were improved by thickness variation. So color conversion glasses with good characteristics of both luminous and color properties were attained.

ZnO nanorods were successfully fabricated on Zn foil by chemical bath deposition (CBD) method. The ZnO precursor concentration and immersion time affected the surface morphologies, structure, and electrical properties of the ZnO nanorods. As the precursor concentration increased, the diameter of the ZnO nanorods increased from ca. 50 nm to ca. 150 nm. The thicknesses of the ZnO nanorods were from ca. 1.98μm to ca. 2.08μm. ZnO crystalline phases of (100), (002), and (101) planes of hexagonal wurtzite structure were confirmed by XRD measurement. The fabricated ZnO nanorods showed a photoluminescene property at 380 nm. Especially, the ZnO nanorods deposited for 6 h in solution with a concentration of 0.005M showed a stronger (101) peak than they did (100) or (002) peaks. In addition, these ZnO nanorods showed a good electrical property, with the lowest resistance among the four samples, because the nanorods were densely in contact and relatively without pores. Therefore, a ZnO nanorod substrate is useful as a highly sensitive biochip substrate to detect biomolecules using an electrochemical method.

The electrical properties of a laminated SMD type PTC thermistor for microcircuit protection were investigated as a function of polymer blowing agent addition. Green ceramics for multilayered BaTiO3-based PTCRs were formed by doctor blade method of barium titanate powders; we successfully laminated the sintered ceramic chips to obtain 10 layer chip PTCRs with PTC effect. The sintered density increases with increasing sintering temperature. The electrical properties of the sintered samples were strongly dependent on the calcination and addition of a polymer blowing agent. When BaTiO3 powders containing 0.2 mol% of Y2O3 were calcined at 1000˚C for 2 hrs, the resistivity jump was of 1-2 orders of magnitude. The resistivity at room temperature increases according to the polymer blowing agent addition. Also, the sample using the calcined powder showed a lower resistivity than that of the sample prepared using powders without calcinations. With an increase in the OBSH, the magnitude of the resistivity jumped as a function of the temperature increase. The resistivity of the sintered bodies after the addition of 0.5 wt% polymer blowing agent at 1290˚C for 2 h was shown to be about 8.5Ω·cm; the jump order of the sintered bodies was shown to be on the order of 102.

For the purpose of improving the durability problem, translucent opal glass was fabricated as a substitute for the polycarbonate diffuser of LED lighting. Calcium phosphate was used as an opacifier of opal glass and melted in an electric furnace. The opaque effect was identified according to the change of the cooling procedure. As results, translucent opal glass was obtained by the melting of a batch with a composition of 3.8% calcium phosphate at 1550˚C for 2 hrs and then the cooling of the material in the furnace. For the cooling condition of the glass sample, HTCG (High Temperature Cooled Glass) was found to have better optical properties than LTAG (Low Temperature Annealed Glass). It had excellent optical properties for a diffuser of LED lighting, with no dazzling from direct light due to its high haze value of over 99% and low parallel transmittance value of under 1%. For the thermal properties, it had an expressed thermal expansion coefficient of 5.7×10-6/˚C and a softening point of 876˚C; it also had good thermal properties such as good thermal shock resistance and was easy to apply to the general manufacturing process in the forming of glass tubes and bulbs. Therefore, it is concluded that this translucent opal glass can be used as a glass diffuser material for LED lighting with high heat resistance and high durability; this material is suitable as a substitute for polycarbonate diffusers.

In the limitless competition era of the 21st century, cost reduction is being highlighted as one of survival strategies of businesses. The first item for cost reduction of businesses is logistical costs. The most keenly required thing for this is to remove unnecessary elements, and the best way to realize it to cut down processes using automatic facilities. Packing container in logistics is like a facility. This study is intended to analyze reduction of costs, improvement of business process and reduction of working force through standardization of standardization, and logistics effects through improvement of environmental images in enterprises.

This paper focuses on the spatial analysis of traditional houses in Huizhou during the Ming and Qing period in China. It first reviews the spatial characteristics of the houses in Huizhou. Typical configurations, spatial elements and spatial compositions of the houses are briefly examined. It then discusses how those spatial characteristics are applied to the houses. To do so, the review of existing research and literature on the houses was conducted. For a detailed analysis of the houses, a field survey was performed to collect research materials of the houses and to assess the application of the characteristics in the houses. At times, the plans of the houses were redrawn for a further analysis of the spatial compositions of the houses. Attempts have been made to understand the underlying principles of their spatial organization. For example, Jin (2010) examined the spatial organization of unit plans. Boyd (1989), Berliner (2003) and Dan (2005) similarly categorized the organizational typology of its varying designs. Son(1995) further interpreted the spatial relations of the variety of houses in a comprehensive manner. Nevertheless, their analytic methodology falls short of a complete explanation of the spatial expansion and transformation in the houses. Therefore, this paper examines the basic principles behind the spatial expansion and transformation of a variety of traditional houses in Huizhou. In doing so, it strives to make logical sense of design variations in the houses and reveal the theory behind them.

has the characteristic is controlling the inhibition or promotion of particle growth by adsorbing onto specific facets of platinum nanoparticles. Therefore, in this study, was added to control the shape of platinum nanoparticles during the liquid phase reduction process. Consequently, platinum cubes were synthesized when of 1.1 mol% (with respect to the Pt concentration) was added into the solution. Platinum octahedrons were synthesized when 32 mol% (with respect to the Pt concentration) was added into the solution. These results demonstrate that the metal salt , effectively controlled the relative growth rates of each facet of Pt nano particles.

본 연구에서는 2007년 7월부터 2010년 7월까지 4년 동안 강원도 삼척시에서 산불 유형(비산불조사구: 산불피해를 입지 않은 지역, 수관화: 산불에 의해 교목의 수관까지 전소한 지역, 지표화: 산불에 의해 교목의 수관 하층만 전소한 지역)과 산불 후 식생의 재생정도(산불피해 후 식피의 재생정도가 1/3이하인 지역: 1, 산불피해 후 식피의 재생정도가 1/3 ~ 2/3인 지역: 2, 산불피해 후 식피의 재생정도가 2/3이상인 지역: 3)에 따른 현존생물량과 순생산량을 비교하였다. 비산불조사구(Un), 수관화 발생 조사구(C-1, C-3), 지표화 발생 조사구(G-2)에서 4년간 평균 현존생물량은 각각 181.20±5.39, 62.04±4.38, 131.09±14.83, 63.39±2.72ton·ha-1로 나타났다. 비산불조사구, 수관화 발생 조사구(C-1, C-3), 지표화 발생 조사구(G-2)에서 4년간 평균 순생산량은 각각 4.17±0.56, 3.27±1.56, 11.51±0.53, 2.10±0.31ton·ha-1·yr-1로 나타났다. 각 조사구의 공통수종인 신갈나무의 DH10(지상으로부터 10cm 높이에서의 직경, mm)의 생장률을 비교하여 보면 수관화 발생 조사구(C-1)에서 1.21±0.55mm·yr-1로 가장 높았으며 수관화 발생조사구(C-3), 지표화 발생 조사구(G-2), 비산불조사구(Un)의 순으로 나타났다. 수고생장률로 비교하였을 때 수관화 발생 조사구(C-3)에서 15.43±4.57cm·yr-1로 가장 높았으며 수관화 발생 조사구(C-1), 지표화 발생 조사구(G-2), 비산불조사구(Un)의 순으로 나타났다.

포도즙, 찹쌀, 누룩을 섞어 빚는 우리나라 고유의 포도주 양조 방법을 적용하여 포도막걸리를 제조하고자 하였다. 포도막걸리의 풍미와 색을 고려하여 산 생성능이 크고 술덧의 풍미가 우수한 Fermivin을 양조 효모로 선정하였다. 포도즙의 농도별, 첨가시기에 따른 막걸리에 대한 각각의 관능품질의 평가 결과 원료 멥쌀의 20%에 해당하는 포도 농축액을 첨가하여 발효시킨 시험구에서 풍부하고 조화로운 풍미를 나타내었으나, 발효과정에서 포도 고유의 색 소실이 확인되었으므로 색도 보완을 위하여 발효 원료로 흑미 첨가에 대하여 검토한 결과 흑미 첨가에 따라 적색도의증가 및 색도에 대한 선호도 개선이 확인되었다. 이와 같은 결과로부터 주세법 기준에 적합하고, 포도 고유의 색을 유지하면서 풍미가 우수한 포도막걸리 발효 조건으로 원료 멥쌀의 20%에 해당하는 포도 농축액과 흑미 2.5%를 첨가하여 Fermivin으로 발효하는 것이 포도막걸리 양조에 적합한 것으로 판단되었다.

TiO2 thin films consisting of positively charged poly(diallyldimethylammonium chloride)(PDDA) and negatively charged titanium(IV) bis(ammonium lactato) dihydroxide(TALH) were successfully fabricated on glass beads by a layer-by-layer(LBL) self-assembly method. The glass beads used here showed a positive charge in an acid range and negative charge in an alkaline range. The glass beads coated with the coating sequence of(PDDA/TALH)n showed a change in the surface morphology as a function of the number of bilayers. When the number of bilayers(n) of the(PDDA/TALH) thin film was 20, Ti element was observed on the surface of the coated glass beads. The thin films coated onto the glass beads had a main peak of the (101) crystal face and were highly crystallized with XRD diffraction peaks of anatase-type TiO2 according to an XRD analysis. In addition, the TiO2 thin films showed photocatalytic properties such that they could decompose a methyl orange solution under illumination with UV light. As the number of bilayers of the(PDDA/TALH) thin film increased, the photocatalytic property of the TiO2-coated glass beads increased with the increase in the thin film thickness. The surface morphologies and optical properties of glass beads coated with TiO2 thin films with different coating numbers were measured by field emission scanning electron microscopy(FE-SEM), X-ray diffraction(XRD) and by UV-Vis spectrophotometry(UV-vis).

본 연구는 차나무(Camellia sinensis L.)와 동백나무(C.japonica L.), 제주지역의 주요 과수작물인 귤나무(Citrus unshiu M.) 잎을 대상으로 엽록소형광과 CO2 흡수능을 비교 분석하여 탄소흡수원으로서의 가치를 평가하고자하였다. 차나무의 CO2 고정율은 같은 과의 동백나무보다 높고 과수작물인 귤나무와 유사하였다. 기공전도도 (gs)는 3종 모두 새벽에는 높고 이후 저녁 시간까지 계속하여 감소하였다. 엽육 내 CO2 농도 (Ci)는 3종 모두 새벽(06:00)에 높고 낮에 감소하였다가 저녁에 다시 증가하는 경향을 보였으며, 잎의 증산율 (E)은 낮 시간에 높아졌다가 저녁에 감소하였다. 차나무에서 광계II의 광화학적 효율(Fv/Fm)은 낮시간에 다소 낮아졌다가 저녁에 다시 증가하는 양상을 보였다. 이러한 낮시간의 Fv/Fm 감소는 광억제의 결과로 보이며 그 감소폭이 동백나무보다 적어 빛이나 고온 등에 내성을 가지고 있음을 알 수 있다. 엽면적당 활성상태의 반응중심의 상대적 밀도를 의미하는 RC/CS는 3종 모두 낮시간에 감소하였다. ABS/RC, TRo/RC, ETo/RC와 DIo/RC는 차나무와 동백나무에서 낮시간에 증가하였으며, 귤나무에서도 낮시간에 증가하였으나 유의성이 없는 것으로 나타났다. 일동화율은 차나무가 320.1 mmol m-2 d-1로 가장 높았으며, 귤나무와 동백나무는 각각 292.5 mmol m-2 d-1와 244.8 mmol m-2 d-1로 나타났다. 이상의 결과를 토대로 차나무는 광합성율이 높고 낮 시간의 광억제도 낮을 뿐만 아니라, 귤나무보다 수분요구량이 낮고 수분이용효율은 높아 탄소흡수원으로서 유용한 작물수종인 것으로 보인다.