대표적인 초식곤충인 나방은 기주식물 특이성을 갖고 있어 기주식물 분포에 따른 식생구조나 서식지 유형을 이해하는데 사용이 가능한 분류군이다. 나방은 종 다양성이 높고 분류학적으로 잘 알려져 있어 조사가 많이 이루 어져 풍부한 데이터가 존재하여 이들의 공간적, 시간적 규모의 생물량 변화 추세를 확인할 수 있다. 본 연구에서는 공간적인 유형에 따라 나방의 생물량을 비교하고자 하였다. 생물량을 추정하기 위해 이용된 분류군은 자나방과, 밤나방과, 태극나방과로 이들 분류군의 앞날개 길이를 기준으로 종별로 계산을 하였다. 공간적인 유형은 숲의 위치(연속된 숲, 파편화된 숲)와 숲의 구성(침엽수림, 활엽수림, 혼효림)을 사용하였다. 그 결과 숲의 위치에 따라 생물량은 차이가 존재했지만(F = 16.76, P < 0.001), 숲의 구성(F = 1.54, P = 0.22)과 숲 위치와 구성의 상호작용은(F = 0.34, P = 0.71) 생물량의 차이를 확인하지 못하였다. 숲 구성에 따라 차이가 나타날 것으로 예상하였지만 나타나 지 않은 데에는 추후 분류군을 더 늘려 확인하는 것이 필요하다. 또한 식물 생물량 추정을 통한 곤충과 먹이자원의 가용 관계를 파악하는 연구도 필요할 것으로 예상한다.

본 연구는 성별다양성이 남성과 여성의 자발적 이직에 미치는 영향을 조사하였다. 본 연구는 성별다양 성을 Blau 지수로 정의하고 남성과 여성의 자발적 이직에 미치는 영향을 확인하였다. 한국노동연구원의 사업체 패널 자료 2007년에서 2013년까지 중 4개년치의 자료를 이용하여 사무직종 중심의 사업장 중 남 성 구성원이 여성 구성원보다 많은 사업장만을 대상으로 패널분석을 실시하였다. 연구 결과에 의하면 성 별다양성은 남성의 자발적 이직에 유의한 정(+)적 영향을 미쳤으며, 여성의 자발적 이직에는 유의한 부 (-)적 영향을 미쳤다. 성별다양성의 증가로 인해 기존 주류집단이었던 남성 구성원들의 유사성과 매력이 감소하였기 때문에 남성의 자발적 이직은 증가했을 것으로 판단된다. 또한 성별다양성의 증가는 소수집 단이 차별받지 않고 일할 환경을 형성하고 조직에 대한 신뢰와 만족감을 증가시키기 때문에 여성의 자발 적 이직을 감소시켰을 것이다. 이는 주류집단이 남성인 조직에서 성별다양성의 증가가 여성 집단과 남성 집단의 이직률에 다른 영향을 미치는 것을 보여주는 결과이다. 또한 최초 지배 성별을 고려하는 것과 고 려하지 않는 것의 결과 차이를 비교해보기 위해 추가분석을 실시하였다. 주요 직종이 사무직종인 모든 사업장을 대상으로 성별다양성이 남성과 여성의 자발적 이직에 미치는 영향을 검증하였다. 성별다양성은 남성의 자발적 이직에 유의한 영향을 미치지 않는 것으로 나타났으며, 여성의 자발적 이직에는 유의한 영향을 미치는 것으로 나타났다. 즉, 최초 지배 성별을 고려하는 것과 고려하지 않는 것은 결과에 차이가 있었다. 이러한 결과들은 최초 지배 성별을 구분하여 성별다양성 연구를 진행해야 함을 시사한다. 후속 연구에서는 최신 데이터를 포함한 종단 자료를 활용하여, 다양한 업종과 직종을 대상으로 성별다양성이 남성과 여성의 자발적 이직에 미치는 차별적인 영향을 분석하는 시도가 필요할 것으로 판단된다.

For the selective catalytic reduction of NOx with ammonia (NH3-SCR), a V2O5WO3/TiO2 (VW/nTi) catalyst was prepared using V2O5 and WO3 on a nanodispersed TiO2 (nTi) support by simple impregnation process. The nTi support was dispersed for 0~3 hrs under controlled bead-milling in ethanol. The average particle size (D50) of nTi was reduced from 582 nm to 93 nm depending on the milling time. The NOx activity of these catalysts with maximum temperature shift was influenced by the dispersion of the TiO2. For the V0.5W2/nTi-0h catalyst, prepared with 582 nm nTi-0h before milling, the decomposition temperature with over 94 % NOx conversion had a narrow temperature window, within the range of 365-391 °C. Similarly, the V0.5W2/nTi-2h catalyst, prepared with 107 nm nTi-2h bead-milled for 2hrs, showed a broad temperature window in the range of 358~450 °C. However, the V0.5W2/Ti catalyst (D50 = 2.4 μm, aqueous, without milling) was observed at 325-385 °C. Our results could pave the way for the production of effective NOx decomposition catalysts with a higher temperature range. This approach is also better at facilitating the dispersion on the support material. NH3-TPD, H2-TPR, FT-IR, and XPS were used to investigate the role of nTi in the DeNOx catalyst.

The synthesis of porous W by freeze-casting and vacuum drying is investigated. Ball-milled WO3 powders and tert-butyl alcohol were used as the starting materials. The tert-butyl alcohol slurry is frozen at –25oC and dried under vacuum at –25 and –10oC. The dried bodies are hydrogen-reduced at 800oC and sintered at 1000oC. The XRD analysis shows that WO3 is completely reduced to W without any reaction phases. SEM observations reveal that the struts and pores aligned in the tert-butyl alcohol growth direction, and the change in the powder content and drying temperature affects the pore structure. Furthermore, the struts of the porous body fabricated under vacuum are thinner than those fabricated under atmospheric pressure. This behavior is explained by the growth mechanism of tert-butyl alcohol and rearrangement of the powders during solidification. These results suggest that the pore structure of a porous body can be controlled by the powder content, drying temperature, and pressure.

The effects of drying temperature on the microstructure of porous W fabricated by the freeze-casting process of tert-butyl alcohol slurry with WO3 powder was investigated. Green bodies were hydrogen-reduced at 800oC for 1 h and sintered at 1000oC for 6 h. X-ray diffraction analysis revealed that WO3 powders were completely converted to W without any reaction phases by hydrogen reduction. The sintered body showed pores aligned in the direction of tertbutyl alcohol growth, and the porosity and pore size decreased as the amount of WO3 increased from 5 to 10v ol%. As the drying temperature of the frozen body increased from -25oC to -10oC, the pore size and thickness of the struts increased. The change in microstructural characteristics based on the amount of powder added and the drying temperature was explained by the growth behavior of the freezing agent and the degree of rearrangement of the solid powder during the solidification of the slurry.

New triple tungstate phosphors NaPbLa(WO4)3:Yb3+/Ho3+ (x = Yb3+/Ho3+ = 7, 8, 9, 10) are successfully fabricated by microwave assisted sol-gel synthesis and their structural and frequency upconversion (UC) characteristics are investigated. The compounds crystallized in the tetragonal space group I41/a and the NaPbLa(WO4)3 host have unit cell parameters a = 5.3927(1) and c = 11.7961(3) Å, V = 343.05(2) Å3, Z = 4. Under excitation at 980 nm, the phosphors have yellowish green emissions, which are derived from the intense 5S2/ 5F4 → 5I8 transitions of Ho3+ ions in the green spectral range and strong 5F5 → 5I8 transitions in the red spectral range. The optimal Yb3+:Ho3+ ratio is revealed to be x = 9, which is attributed to the quenching effect of Ho3+ ions, as indicated by the composition dependence. The UC characteristics are evaluated in detail under consideration of the pump power dependence and Commission Internationale de L'Eclairage chromaticity. The spectroscopic features of Raman spectra are discussed in terms of the superposition of Ho3+ luminescence and vibrational lines. The possibility of controlling the spectral distribution of UC luminescence by the chemical content of tungstate hosts is demonstrated.

In this study, we prepare pure WO3 inverse opal(IO) film with a thickness of approximately 3 μm by electrodeposition, and an ultra-thin TiO2 layer having a thickness of 2 nm is deposited on WO3 IO film by atomic layer deposition. Both sets of photoelectrochemical properties are evaluated after developing dye-sensitized solar cells(DSSCs). In addition, morphological, crystalline and optical properties of the developed films are evaluated through field-emission scanning electron microscopy(FE-SEM), High-resolution transmission electron microscopy(HR-TEM), X-ray diffraction(XRD) and UV/ visible/infrared spectrophotometry. In particular, pure WO3 IO based DSSCs show low VOC, JSC and fill factor of 0.25 V, 0.89 mA/cm2 and 18.9 %, achieving an efficiency of 0.04 %, whereas the TiO2/WO3 IO based DSSCs exhibit VOC, JSC and fill factor of 0.57 V, 1.18 mA/cm2 and 50.1 %, revealing an overall conversion efficiency of 0.34 %, probably attributable to the high dye adsorption and suppressed charge recombination reaction.

“W si wo le” and “W si wo suanle” are two constructions commonly used in modern Chinese spoken language, and they all have a high degree of meaning. The two constructions can sometimes be used interchangeably, there will be some subtle differences in semantics after the switchover; but in some cases, the two are not interchangeable. According to the corpus survey, we found that “W si wo le” is much more commonly used than“W si wo suanle” . “W si wo suanle” as a new construction is used only in a specific context in spoken Chinese, “suanle”as an extremely important component of the construction “W si wo suanle” must affect the choice of the variable W, the meaning of this construction and the syntactic features of this construction. This paper intents to compare the similarities and differences of “W si wo le” and “W si wo suanle” on the use and characteristics of the variable W, the construction meaning and the syntactic features ,we also try to analyze and explain the causes of these differences.

Tungsten trioxide (WO3) is a promising candidate as a photocatalyst because of its outstanding electrical and optical properties. In this study, we prepare WO3 thin films by electrodeposition and characterize the photocatalytic degradation of methylene blue using these films. Depending on the voltage conditions (static and pulse), compact and porous WO3 films are fabricated on a transparent ITO/glass substrate. The morphology and crystal structure of electrodeposited WO3 thin films are investigated by scanning electron microscopy, atomic force microscopy, and X-ray diffraction. An application of static voltage during electrodeposition yields a compact layer of WO3, whereas a highly porous morphology with nanoflakes is produced by a pulse voltage process. Compared to the compact film, the porous WO3 thin film shows better photocatalytic activities. Furthermore, a much higher reaction rate of degradation of methylene blue can be achieved after post-annealing of WO3 thin films.

W-10 wt% Ti alloys that have a homogeneous microstructure are prepared by thermal decomposition of WO3-TiH2 powder mixtures and spark plasma sintering. The reduction and dehydrogenation behavior of WO3 and TiH2 are analyzed by temperature programmed reduction and a thermogravimetric method, respectively. The X-ray diffraction analysis of the powder mixture, heat-treated in an argon atmosphere, shows W- oxides and TiO2 peaks. Conversely, the powder mixtures heated in a hydrogen atmosphere are composed of W, WO2 and TiO2 phases at 600 ℃ and W and W-rich β phases at 800 ℃. The densified specimen by spark plasma sintering at 1500 ℃ in a vacuum using hydrogen-reduced WO3-TiH2 powder mixtures shows a Vickers hardness value of 4.6 GPa and a homogeneous microstructure with pure W, β and Ti phases. The phase evolution dependent on the atmosphere and temperature is explained by the thermal decomposition and reaction behavior of WO3 and TiH2.

Composites of P25 TiO2 and hexagonal WO3 nanorods are synthesized through ball-milling in order to study photocatalytic properties. Various composites of TiO2/WO3 are prepared by controlling the weight percentages (wt%) of WO3, in the range of 1–30 wt%, and milling time to investigate the effects of the composition ratio on the photocatalytic properties. Scanning electron microscopy, x-ray diffraction, and transmission electron microscopy are performed to characterize the structure, shape and size of the synthesized composites of TiO2/WO3. Methylene blue is used as a test dye to analyze the photocatalytic properties of the synthesized composite material. The photocatalytic activity shows that the decomposition efficiency of the dye due to the photocatalytic effect is the highest in the TiO2/ WO3 (3 wt%) composite, and the catalytic efficiency decreases sharply when the amount of WO3 is further increased. As the amount of WO3 added increases, dye-removal by adsorption occurs during centrifugation, instead of the decomposition of dyes by photocatalysts. Finally, TiO2/WO3 (3 wt%) composites are synthesized with various milling times. Experimental results show that the milling time has the best catalytic efficiency at 30 min, after which it gradually decreases. There is no significant change after 1 hour.

The present study demonstrates the effect of raw powder on the pore structure of porous W-Ni prepared by freeze drying of camphene-based slurries and sintering process. The reduction behavior of WO3 and WO3-NiO powders is analyzed by a temperature programmed reduction method in Ar-10% H2 atmosphere. After heat treatment in hydrogen atmosphere, WO3- NiO powder mixture is completely converted to metallic W without any reaction phases. Camphene slurries with oxide powders are frozen at −30 oC, and pores in the frozen specimens are generated by sublimation of the camphene during drying in air. The green bodies are hydrogen-reduced at 800 oC and sintered at 1000 oC for 1 h. The sintered samples show large and aligned parallel pores to the camphene growth direction, and small pores in the internal wall of large pores. The strut between large pores, prepared from pure WO3 powder, consists of very fine particles with partially necking between the particles. In contrast, the strut densification is clearly observed in the Ni-added W sample due to the enhanced mass transport in activation sintering.

In2O3 doped WO3 powders were prepared by a polymer solution route and their NO2 gas sensing properties were analyzed. The synthesized powders showed nano-sized particles with specific surface areas of 6.01~21.5 m2/g and the particle size and shape changed according to the content of In2O3. The gas sensors fabricated with the synthesized powders were tested at operating temperatures of 400~500 oC and 100~500 ppm concentrations of NO2 atmosphere. The particle size and In2O3 content affected on the initial sensor resistance in an air atmosphere. The highest sensitivity (8.57 at 500 oC), which was 1.77 higher than the sensor consisting of the pure WO3 sample, was measured in the 0.5 mol% In2O3 doping sample. In addition, the response time and recovery time were improved by the addition of In2O3.

Transition-metal oxide semiconductors have various band gaps. Therefore, many studies have been conducted in various application fields. Among these, methods for the adsorption of organic dyes and utilization of photocatalytic properties have been developed using various metal oxides. In this study, the adsorption and photocatalytic effects of WO3 nanomaterials prepared by hydrothermal synthesis are investigated, with citric acid added in the hydrothermal process as a structure-directing agent. The nanostructures of WO3 are studied using transmission electron microscopy and scanning electron microscopy images. The crystal structure is investigated using X-ray diffraction patterns, and the changes in the dye concentrations adsorbed on WO3 nanorods are measured with a UV-visible absorption spectrophotometer based on Beer-Lambert’s law. The methylene blue (MB) dye solution is subjected to acid or base conditions to monitor the change in the maximum adsorption amount in relation to the pH. The maximum adsorption capacity is observed at pH 3. In addition to the dye adsorption, UV irradiation is carried out to investigate the decomposition of the MB dye as a result of photocatalytic effects. Significant photocatalytic properties are observed and compared with the adsorption effects for dye removal.

Porous W-10 wt% Ti alloys are prepared by freeze-drying a WO3-TiH2/camphene slurry, using a sintering process. X-ray diffraction analysis of the heat-treated powder in an argon atmosphere shows the WO3 peak of the starting powder and reaction-phase peaks such as WO2.9, WO2, and TiO2 peaks. In contrast, a powder mixture heated in a hydrogen atmosphere is composed of the W and TiW phases. The formation of reaction phases that are dependent on the atmosphere is explained by a thermodynamic consideration of the reduction behavior of WO3 and the dehydrogenation reaction of TiH2. To fabricate a porous W-Ti alloy, the camphene slurry is frozen at -30℃, and pores are generated in the frozen specimens by the sublimation of camphene while drying in air. The green body is hydrogen-reduced and sintered at 1000℃ for 1 h. The sintered sample prepared by freeze-drying the camphene slurry shows large and aligned parallel pores in the camphene growth direction, and small pores in the internal walls of the large pores. The strut between large pores consists of very fine particles with partial necking between them.

A Nanosized WO3 and CuO powder mixture is prepared using novel high-energy ball milling in a bead mill to obtain a W-Cu nanocomposite powder, and the effect of milling time on the structural characteristics of WO3-CuO powder mixtures is investigated. The results show that the ball-milled WO3-CuO powder mixture reaches at steady state after 10 h milling, characterized by the uniform and narrow particle size distribution with primary crystalline sizes below 50 nm, a specific surface area of 37 m2/g, and powder mean particle size (D50) of 0.57 μm. The WO3-CuO powder mixtures milled for 10 h are heat-treated at different temperatures in H2 atmosphere to produce W-Cu powder. The XRD results shows that both the WO3 and CuO phases can be reduced to W and Cu phases at temperatures over 700oC. The reduced W-Cu nanocomposite powder exhibits excellent sinterability, and the ultrafine W-Cu composite can be obtained by the Cu liquid phase sintering process.

Lee, Jee Won. 2017. “The Use and Discourse-Pragmatic Function of wo buzhidao in Naturally Occurring Mandarin Chinese Conversation”. The Sociolinguistic Journal of Korea 25(1). 167~192. This study investigates several aspects of Chinese (wo) buzhidao using both qualitative and quantitative methods, including its distributional properties and discourse-pragmatic functions in conversational contexts. This study has found that (wo) buzhidao occurs in conversational environments other than in reply to information questions and carries more interactive and social implications than had been previously proposed by previous studies. First, (wo) buzhidao marks the speaker’s uncertainty and concerns about the truth of the proposition expressed. Second, (wo) buzhidao constructs the speaker’s neutral position by disattending opinions, assessments, or troubles. Third, (wo) buzhidao avoids an explicit disagreement. The use of (wo) buzhidao as a stance marker allows the speaker to convey his/her consideration for the hearer’s face, and it can help to achieve a range of interactional goals. Native speakers of Mandarin Chinese employ (wo) buzhidao in conjunction with other interactive strategies to organize their speech via their recipient enabling mutual intersubjectivity.

The effects of the heat treatment temperature and of the atmosphere on the dehydrogenation and hydrogen reduction of ball-milled TiH2-WO3 powder mixtures are investigated for the synthesis of Ti-W powders with controlled microstructure. Homogeneously mixed powders with refined TiH2 particles are successfully prepared by ball milling for 24 h. X-ray diffraction (XRD) analyses show that the powder mixture heat-treated in Ar atmosphere is composed of Ti, Ti2O, and W phases, regardless of the heat treatment temperature. However, XRD results for the powder mixture, heat-treated at 600oC in a hydrogen atmosphere, show TiH2 and TiH peaks as well as reaction phase peaks of Ti oxides and W, while the powder mixture heat-treated at 900oC exhibits only XRD peaks attributed to Ti oxides and W. The formation behavior of the reaction phases that are dependent on the heat treatment temperature and on the atmosphere is explained by thermodynamic considerations for the dehydrogenation reaction of TiH2, the hydrogen reduction of WO3 and the partial oxidation of dehydrogenated Ti.

Ho3+/Yb3+/Tm3+ tri-doped NaY1-x(WO4)2 phosphors with proper doping concentrations of Ho3+, Yb3+ and Tm3+ (x = Ho3+ +Yb3+ +Tm3+, Ho3+ = 0.04, 0.03, 0.02, 0.01, Yb3+ = 0.35, 0.40, 0.45, 0.50 and Tm3+ = 0.01, 0.02, 0.03, 0.04) were successfully synthesized via the microwave sol-gel route, and their upconversion properties were investigated. Well-crystallized microcrystalline particles showed fine and homogeneous microcrystalline morphology with particle sizes of 1-2 μm. The optical properties were comparatively examined using photoluminescence emission and Raman spectroscopy. Under excitation at 980 nm, the doped particles exhibited white emissions based on blue, green and red emission bands, which correspond to the 1G4→ 3H6 transitions of Tm3+ in the blue region, the 5S2/ 5F4→ 5I8 transitions of Ho3+ in the green region, the 5F5→ 5I8 transitions of Ho3+, and the 1G4→ 3F4 and 3H4→ 3H6 transitions of Tm3+ in the red region. The pump power dependence of the upconversion emission intensity and the Commission Internationale de L'Eclairage chromaticity coordinates of the phosphors were evaluated in detail.