그래핀 산화물(GO), 폴리에틸렌 글리콜 다이아크릴레이트(PEGDA), 폴리에틸렌 글리콜 메틸 에터 아크릴레이트 (PEGMEA)의 나노복합체를 자외선 광중합을 통해 합성하였다. GO는 가교된 폴리에틸렌 옥사이드(XPEO) 매트릭스 내에 최 대 1.0 wt% 농도까지 균일하게 분산시켰다. 더 높은 농도에서는 GO가 응집되는 경향을 보였다. 잘 분산된 GO는 친수성 PEO 사슬과 추가적인 화학적 가교 네트워크를 형성했다. XPEO-GO 나노복합체는 GO 농도에 따라 기계적 강도 및 염과 가 스에 대한 차단 특성이 향상된 것으로 나타났다. 이 연구는 다양한 GO 농도와 플레이크 크기를 가진 XPEO-GO 하이드로겔 의 제조 및 특성화를 다루고 있다. 이러한 특성은 나노복합 하이드로겔이 강화된 XPEO 기반 바이오소재 및 고급 항균성 한 외여과(UF) 친수성 코팅에서의 잠재적 응용 가능성을 시사한다.

This study investigates the behavior of the thermal conductivity among material properties in order to develop a thermal evaluation methodology of spent fuel assembles in a transport cask. It is inefficient to model each element of the spent fuel assembly in detail, and it is generally calculated by modeling the effective thermal conductivity (ETC). The ETC model was developed to allow a much simpler representation of a spent fuel assembly within a fuel compartment by treating the entire spent fuel rod array and the surrounding fill gas within the confines of the compartment as a homogenous solid material. The fuel rod assembly and surrounding gas are modeled with an effective conductivity that is designed to yield an overall conduction heat transfer rate that is equivalent to the combined effect of local conduction and radiation heat transfer in a plane through the assembly. When this model is applied to the transport cask, it tends to predict the cladding peak temperature lower than the results of detailed model in which the fuel rod arrangement and shape of the fuel assembly are simulated. As for the tendency of the error, the model tended to under-predict when basket temperature was lower than a certain temperature, and over-predict when it was higher. The purpose of this study is to investigate the attenuation effect of the cladding peak temperature on the related variables when the ETC model is applied to the transport cask. In addition, based on the thermal characteristics of this model, a correction factor that can compensate for this attenuation effect is presented. This correction factor is obtained by finding the difference between a separate ETC homogeneous model and a separate detailed fuel model, rather than directly applying the ETC calculated from the detailed fuel model to the transport cask.

Low- and intermediate-level radioactive wastes have been disposed of in the first-phase deep underground silo disposal at Gyeongju in South Korea. These radioactive wastes contain harmful radionuclides such as Uranium-238 (238U), which can pose long-term and deleterious effects on humans and the natural environment. Ethylenediaminetetraacetic acid and isosaccharinic acid, which can be formed via cellulosic waste degradation under high alkaline conditions might considerably enhance the transport behavior of 238U with the intrusion of rainwater and groundwater. In this study, the engineered barriers (concrete and grout) and natural barriers (sedimentary rock and granite) were used to investigate the 238U transport behavior in artificial cementitious porewater of State I (pH 13.3) and State II (pH 12.5) based on groundwater or rainwater. The surface properties and geochemical compositions of barrier samples were characterized using XRD, XRF, SEM-EDX, and BET. The transport behaviors of 238U in various solution conditions were observed by sorption distribution coefficient (Kd) at a range of initial chelating agents concentration (10-5-10-2 M). The sorption behavior of 238U was retarded more in the engineered rock barriers than in the natural rock barriers. The mobility enhancement of 238U was more significant in State I than in State II. In comparison with the absence of chelating agents, negligible changes in the Kd values of 238U were observed at less than initial chelating agent concentrations of 10-4 M. However, the Kd values of 238U were significantly reduced at initial chelating agent concentrations higher than 10-3 M. Therefore, these experimental findings show that the transport behavior of 238U into the geo- and bio-sphere could be accelerated by the presence of chelating agents and the type of cement degradation states.

The “shadow zone” is defined as a region below a flow obstacle, such as a vault, in unsaturated soils. Due to the capillary discontinuity of the cavity, water saturation on the top and side of the cavity is higher than the ambient saturation. On the bottom of the cavity, however, there is a region where water saturation is lower than ambient saturation. Undoubtedly, a shadow zone may also exist below a LILW disposal vault built in subsurface soils above the water table before the vault is fully degraded. During the degradation, flow in the shadow zone is controlled by the rate of water infiltrating the degrading vault. In this study, as one of the efforts to be made for enhancing safety margin by a realistic safety assessment of the engineered vault type LILW disposal facility, the shadow zone effect is investigated by a numerical parametric study using AMBER code. The conceptual model and data were excerpted from IAEA, ISAM Vault Test Case for the liquid release design scenario. It is assumed that the nearfield barriers degrade with time. In order to compare a visible shadow zone effect, the vault degradation period is assumed to be both 500 and 1,000 years, and the shadow zone depth to be varied according to unsaturated zone lithology. It can be seen that with a shorter shadow zone (2.7 m), radionuclides arrive at the water table earlier than with a full shadow zone (55 m) due to increased advection rate in the unsaturated zone. This effect tends to be more visible in the case of a longer degradation period. For radionuclides with short residence time relative to their half-lives in the unsaturated zone, such as Tc-99 and I-129, the radionuclides are shown to come out because they will arrive sooner, thereby allowing less peak release rate, when the shadow zone effect is considered. Once the vault is completely degraded and the infiltration rate of water flowing through the vault is equal to the ambient rate, the shadow zone effect disappears. In this example calculations using IAEA ISAM Vault Test Case input parameters, it might not be shown a significant shadow zone effect. Nevertheless, when the extent of the shadow zone is determined through more sophisticated hydraulic studies in the unsaturated soils surrounding the vault, the shadow zone effect would be checked up on the realistic near-field radionuclide transport modeling in order to contribute to gaining safety margins for post-closure safety assessment of the Wolsong 2nd phase LILW disposal facility.

본 연구에서는 고분자 전해질막을 구성하고 있는 고분자 주쇄의 반복단위 개수를 변경해 가며 수화채널 모폴로지 와 이온전도도의 변화를 비교하였고, 최종적으로 분자동역학 전산모사 수행 시에 적정한 고분자 모델을 선정하기 위한 기준 을 제시하고자 하였다. 고분자 주쇄의 길이가 가장 짧은 모델에서 주쇄 및 술폰산기의 움직임이 커지는 것을 관찰할 수 있었 지만, 수화채널 모폴로지는 특별한 상관관계를 발견할 수 없었다. 또한, 수화채널 모폴로지에 가장 큰 영향을 받는 수소이온 전달 능력의 특성 상, 수소이온 전도도에서도 고분자 주쇄의 길이와 큰 상관관계를 보이지는 않았다. 이러한 결과는 특히 바 인더용 이오노머 제조에 대한 중요한 정보를 제공한다. 일반적으로 바인더용 이오노머의 경우 고분자 전해질막 소재를 저분 자량으로 합성하여 사용하게 되는데, 이때 주쇄/술폰산기의 움직임이 향상되므로 촉매층을 잘 둘러싸는 역할을 할 수 있는 반면에, 수소이온 전달 능력 자체에 있어서는 특별한 변화가 없을 것을 예상할 수 있다. 결론적으로, 바인더용 이오노머 제조 시에는 수소이온 전달 성능보다는 물성에 좀 더 초점을 맞추어 분자량 및 구조 설계가 필요할 것이다.

본 연구에서는 분자동역학에서 원자의 움직임을 정의하는 가장 중요한 요소인 force-field가 실제 고분자 및 기체 분자의 움직임에 어떠한 영향을 주는지 알아보고자 하였다. Repeat unit과 고분자 구조는 본 연구에서 사용된 5종의 force-field 에서 모두 정상적으로 작용을 하였고, 최종 고분자 3D 모델에서 고분자 linear chain의 분포에서도 큰 차이를 보이지 않았다. 그러나 실제 기체 분자의 움직임은 매우 다른 경향을 나타내었으며, 이는 같은 functional form을 사용하는 COMPASS와 pcff 에서도 관찰되었다. 따라서 동일한 구조라고 하더라도 기체 분자의 운동은 시간에 따라 지속적으로 force-field의 영향 하에서 움직이기 때문에, 고분자 linear chain과 같은 거대 분자에 비하여 그 영향을 훨씬 크게 받는다는 것을 알 수 있으며, 결론적으로 서로 다른 force-field의 사용 시에는 결과 비교에 있어서도 매우 신중을 기해야 할 것이다.

ZnO micro/nanocrystals are formed by a vapor transport method. Mixtures of ZnO and TiO powders are used as the source materials. The TiO powder acts as a reducing agent to reduce the ZnO to Zn and plays an important role in the formation of ZnO micro/nanocrystals. The vapor transport process is carried out in air at atmospheric pressure. When the weight ratios of TiO to ZnO in the source material are lower than 1:2, no ZnO micro/nanocrystals are formed. However, when the ratios of TiO to ZnO in the source material are greater than 1:1, the ZnO crystals with one-dimensional wire morphology are formed. In the room temperature cathodoluminescence spectra of all the products, a strong ultraviolet emission centered at 380 nm is observed. As the ratio of TiO to ZnO in the source material increases from 1:2 to 1:1, the intensity ratio of ultraviolet to visible emission increases, suggesting that the crystallinity of the ZnO crystals is improved. Only the ultraviolet emission is observed for the ZnO crystals prepared using the source material with a TiO/ZnO ratio of 2:1.

Effect of the nonuniform grid on the two-dimensional transport equation was investigated in terms of theoretical analysis and finite difference method (FDM). The nonuniform grid having a typical structure of the numerical weather forecast model was incorporated in the vertical direction, while the uniform grid was used in the zonal direction. The staggered and non-staggered grid were placed in the vertical and zonal direction, respectively. Time stepping was performed with the third-order Runge Kutta scheme. An error analysis of the spatial discretization on the nonuniform grid was carried out, which indicated that the combined effect of the nonuniform grid and advection velocity produced either numerical diffusion or numerical adverse-diffusion. An analytic function is used for the quantitative evaluation of the errors associated with the discretized transport equation. Numerical experiments with the non-uniformity of vertical grid were found to support the analysis.

Recent Engineered nanoparticles were increasingly exposed to environmental system with the wide application and production of nanomaterials, concerns are increasing about their environmental risk to soil and groundwater system. In order to assess the transport behavior of silver nanoparticles (AgNPs), a saturated packed column experiments were examined. Inductively coupled plasma-mass spectrometry and a DLS detector was used for concentration and size measurement of AgNPs. The column experiment results showed that solution chemistry had a considerable temporal deposition of AgNPs on the porous media of solid glass beads. In column experiment, comparable mobility improvement of AgNPs were observed by changing solution chemistry conditions from salts (in both NaCl and CaCl2 solutions) to DI conditions, but in much lower ionic strength (IS) with CaCl2. Additionally, the fitted parameters with two-site kinetic attachment model form the experimental breakthrough curves (BTCs) were associated that the retention rates of the AgNPs aggregates were enhanced with increasing IS under both NaCl and CaCl2 solutions.

Flat sheet membranes consisting of a selective layer and a porous support usually require gutter layer to reduce the bulk pores of the substrates. The gutter layer mitigates the geometric restrictions of support, which enables selective layer to have defect-free morphology with thin thickness (< 100 nm). For this reason, the gutter layer has been introduced to many industrial membranes, and the systematical studies of the effects of the gutter layer properties on membrane performance should be needed. Herein, we introduced several gutter layers with different thicknesses into graphene oxide intercalated polymer TFC membranes to determine the relationship between gutter layer properties and total membrane performances. This study provides more practical insight to determine the optimum gutter layer properties in designing TFC membranes.

바이오매스로부터 생산되는 수송용 바이오연료는 온실가스 저감과 지속가능하고 친환경적으 로 석유제품을 대체할 수 있다. 수송용 바이오연료의 의무혼합과 보급 목표는 유럽연합, 미국 등의 많은 나라에서 발표하였고 정부의 정책에 의해 활성화되었다. 본 논문에서는 각국의 수송용 바이오연료 정책 과 품질기준에 대해 논하겠다. 유럽연합의 바이오연료는 온실가스를 저감하는 정책으로 이동하였다. 미 국은 RFS2 하에서 바이오연료의 품질기준을 설정하였고 연방 및 주 정부 수준에서 바이오연료를 촉진 하는 정책을 펴고 있다. 한국은 휘발유에 산소 함량 기준으로 2.3%를 산화물로 허용하고 있으며 바이오 디젤은 2015년 7월 31일부터 B2.5로 의무혼합하고 있다.

용액-확산 메커니즘에 의해 결정되는 기존의 고분자에서와는 달리, 촉진수송은 투과도와 선택도를 동시에 향상시킬 수 있는 기술이다. 본 연구에서는 은 나노입자, 폴리비닐피롤리돈, 7,7,8,8-테트라시야노퀴노디메탄으로 구성된 촉진수송 올레핀 분리막에 있어서, 메조기공 티타늄산화물(m-TiO2)에 대한 영향을 연구하였다. 특히 메조기공 티타늄산화물은 폴리비닐클로라이 드-g-폴리옥시에틸렌 메타크릴레이트 가지형 공중합체를 템플레이트로 하여 쉽고 대량 생산이 가능한 방법으로 제조하였다. 엑 스레이 회절분석에 따르면, 제조된 메조기공 티타늄산화물은 아나타제와 루타일 상의 혼합으로 구성되어 있으며, 결정의 크기가 약 16 nm 정도 되었다. 메조기공 티타늄산화물을 첨가하였을 때, 분리막의 확산도가 증가하여 혼합기체 투과도가 1.6에서 16 GPU로 증가하였고 선택도는 45에서 37로 약간 감소하였다. 메조기공 티타늄산화물이 첨가되지 않은 분리막은 장시간 성능이 유지되었으나, 메조기공 티타늄산화물이 첨가된 분리막의 경우 시간이 지남에 따라 투과도와 선택도가 감소하였다. 이는 티타늄 산화물과 은 사이의 화학적 상호작용으로 은 나노입자의 올레핀 운반체로써의 활성을 감소시키기 때문으로 사료된다.

유기태양전지의 투명전극으로서 기존의 값비싸고 깨지기 쉬운 Indium Tin Oxide (ITO) 전극을 대체하고자, 전도성 고분자인 poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS)를 적용하였다. 솔벤트의 도핑 농도에 따른 PEDOT:PSS 박막의 전기 전도도와 표면 거칠기의 특성 변화를 관찰하고, 그 결과가 PEDOT:PSS를 투명전극으로 사용한 유기태양전지의 특성에 미치는 영향을 연구하였다. PEDOT:PSS의 솔벤트 농도가 증가함에 따라, 박막의 표면 거칠기가 증가하고, 이는 유기태양전지의 단락전류의 변화를 야기했다. 또한, 소자의 홀 이동층이 얇아짐에 따라 광활성층의 단파장영역의 광흡수가 증가하는 것을 관찰할 수 있었다.