Since the directly bonded interface between TiAl alloy and SCM440 includes lots of cracks and generated intermetallic compounds(IMCs) such as TiC, FeTi, and Fe2Ti, the interfacial strength can be significantly reduced. Therefore, in this study, Cu is selected as an insert metal to improve the lower tensile strength of the joint between TiAl alloy and SCM440 during friction welding. As a result, newly formed IMCs, such as Cu2TiAl, CuTiAl, and TiCu2, are found at the interface between TiAl alloy and Cu layer and the thickness of IMCs layers is found to vary with friction time. In addition, to determine the relationship between the thickness of the IMCs and the strength of the welded interfaces, a tensile test was performed using sub-size specimens obtained from the center to the peripheral region of the friction-welded interface. The results are discussed in terms of changes in the IMCs and the underlying deformation mechanism. Finally, it is found that the friction welding process needs to be idealized because IMCs generated between TiAl alloy and Cu act to not only increase the bonding strength but also form an easy path of fracture propagation.

There are several manufacturing techniques for developing thermionic cathodes for vacuum ultraviolet(VUV) ionizers. The triple alkaline earth metal emitters(Ca-Sr-Ba) are formulated as efficient and reliable thermo-electron sources with a great many different compositions for the ionizing devices. We prepare two basic suspensions with different compositions: calcium, strontium and barium. After evaluating the electron-emitting performance for europium, gadolinium, and yttrium-based cathodes mixed with these suspensions, we selected the yttrium for its better performance. Next, another transition metal indium and a lanthanide metal neodymium salt is introduced to two base emitters. These final composite metal emitters are coated on the tungsten filament and then activated to the oxide cathodes by an intentionally programmed calcination process under an ultra-high vacuum(~10-6 torr). The performance of electron emission of the cathodes is characterized by their anode currents with respect to the addition of each element, In and Nd, and their concentration of cathodes. Compared to both the base cathodes, the electron emission performance of the cathodes containing indium and neodymium decreases. The anode current of the Nd cathode is more markedly degraded than that with In.

In this study, 40 residents of the Gwangyang and Yeosu areas were assessed for their level of exposure to heavy metals (As, Cd, Ni) from April 2017 to June 2018. The aim was to understand the differences in levels of indoor exposure to heavy metals (As, Cd, Ni), and a health risk assessment was conducted to determine whether there was any fatal cause from carcinogenic elements. The mean concentrations of PM10 particles indoors were As 0.24 μg/m3, Cd 0.07 μg/m3, and Ni 0.89 μg/m3. The health risk assessment for the arsenic, cadmium, and nickel in indoor air confirmed that the mean values exceeded the cancer risk tolerances specified by the U.S. EPA, for As (males 3.07 × 10−4, females 3.35 × 10−4), Cd (males 3.83 × 10−5, females 4.18 × 10−5), and Ni (males 6.36 × 10−5, females 6.95 × 10−5).

Dual porous structures are observed for the first time on a metallic Cu surface underneath anodic Cu oxide by the application of an anodizing voltage to Cu in oxalic acid. The as-prepared porous Cu surface contains macropores of less than 1 μm diameter and mesopores of about tens of nanometers diameter with circular shapes. The size and density (number of pores/area) of the macropores are dependent on the applied voltage. It is likely that the localized dissolution (corrosion) of Cu in oxalic acid under the anodizing voltages is responsible for the formation of the mesopores, and the combination of a number of the mesopores might create the macropores, especially under a relatively high anodizing voltages or a prolonged anodizing time. The variations of pore structure (especailly macropores) with applied voltage and time are reasonably explained on the basis of the proposed mechanism of pore formation.

Layered LiNi0.83Co0.11Mn0.06O2 cathode materials single- and dual-doped by the rare-earth elements Ce and Nd are successfully fabricated by using a coprecipitation-assisted solid-phase method. For comparison purposes, nondoping pristine LiNi0.83Co0.11Mn0.06O2 cathode material is also prepared using the same method. The crystal structure, morphology, and electrochemical performances are characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectrometer (EDS) mapping, and electrochemical techniques. The XRD data demonstrates that all prepared samples maintain a typical α-NaFeO2-layered structure with the R-3m space group, and that the doped samples with Ce and/or Nd have lower cation mixing than that of pristine samples without doping. The results of SEM and EDS show that doped elements are uniformly distributed in all samples. The electrochemical performances of all doped samples are better than those of pristine samples without doping. In addition, the Ce/Nd dualdoped cathode material shows the best cycling performance and the least capacity loss. At a 10 C-rate, the electrodes of Ce/Nd dual-doped cathode material exhibit good capacity retention of 72.7, 58.5, and 45.2% after 100, 200, and 300 cycles, respectively, compared to those of pristine samples without doping (24.4, 11.1, and 8.0%).

In aluminum brazing processes, corrosive flux, which is used in preventing oxidation, is currently raising environmental concerns because it generates many pollutants such as dioxin. The brazing process involving noncorrosive flux is known to encounter difficulties because the melting temperature of the flux is similar to that of the base material. In this study, a new brazing filler material is developed based on aluminum and non-corrosive flux composite powder. To minimize the interference of consolidation aluminum alloy powder by the flux, the flux is intentionally embedded in the aluminum alloy powder using a mechanical milling process. This study demonstrates that the morphology of the composite powder can be varied according to the mixing process, and this significantly affects the relative density and mechanical properties of the final filler samples.

In this study, porous Mo-5 wt% Cu with unidirectionally aligned pores is prepared by freeze drying of camphene slurry with MoO3-CuO powders. Unidirectional freezing of camphene slurry with dispersion stability is conducted at -25℃, and pores in the frozen specimens are generated by sublimation of the camphene crystals. The green bodies are hydrogen-reduced at 750℃ and sintered at 1000℃ for 1 h. X-ray diffraction analysis reveals that MoO3- CuO composite powders are completely converted to a Mo-and-Cu phase without any reaction phases by hydrogen reduction. The sintered bodies with the Mo-Cu phase show large and aligned parallel pores to the camphene growth direction as well as small pores in the internal walls of large pores. The pore size and porosity decrease with increasing composite powder content from 5 to 10 vol%. The change of pore characteristics is explained by the degree of powder rearrangement in slurry and the accumulation behavior of powders in the interdendritic spaces of solidified camphene.

In this paper, the experimental study and finite elements analysis were conducted on homogeneous and dissimilar metals single lap-shear bonded joints to investigate the factor that affect the joint failure load. It was found that factors which have the significant effects on the failure load of the joint was stiffness of the adherends. And from experimental results, it can be confirmed that the failure load increases linearly with overlap length increases. And the failure load of dissimilar metal joints is approximately 1KN(10 ～17%) larger than homogeneous metal joints. In order to confirm this phenomenon, the stress distribution and strain distribution of the specimens were analyzed through the finite element analysis. The difference between homogeneous metals joints and dissimilar metals joints is that stress and strain in adhesive are concentrated at the end of the overlap zone close to aluminium which has lower rigidity than aluminium in case of dissimilar metals joints. From high rigidity of steel, the stress concentration in bonds are decreased and it cause increase of the failure strength at dissimilar metal joints.

중금속이 곤충에 미치는 영향을 조사하기 위하여 빨간집모기 (Culex pipiens pallens) 금속용액 (Cu, Cd, Hg, Pb, Zn)에서 사육한 후 50% 치사농도 (LC50) 용화시기, 총 지질함량, 지질조성, 총 단백질 함량변화를 측정하였다. 50% 치사농도 (LC50)는 3령 유충으로 24시간 처리한 Hg 처리군에서 0.45 mg kg-1으로 나타나 다른 금속에 비해 독성이 강한 것으로 나타났고, 용화 시기는 처리군이 대조군 (129시간)에 비해 지연되었으며 Cd가 처리군 중 273시간으로 가장 늦게 용화되었다. 중금속에 노출된 모기시료에서 총 여섯 종류의 지질 band가 분리되었으며, 이 중 5종의 지질이 동정되었다 (phospholipid, cholesterol, fatty acid, triglyceride, cholesterol ester). 모든 처리군의 총 지질함량은 대조군에 비해 감소하였다. 또한, 대조군의 단백질 함량 (0.51 mg ind.-1)이 처리군의 단백질 함량에 비해 높게 나타났으며, 처리군 중 Hg과 Cd을 처리한 유충의 단백질 함량이 매우 낮게 나타났다. 결론적으로 중금속이 처리된 용액에서 사육된 모기유충은 오염된 환경에 의한 먹이섭취의 장애 및 중금속의 독성으로 인해 단백질 함량과 지질의 감소가 일어나 발육이 느려지고 용화시기가 길어지는 것으로 생각되며 이는 중금속에 의한 체내 물질대사의 변화를 의미한다. 이러한 결과는 중금속 오염이 모기의 생존과 성장을 억제시켜 모기 개체군 크기에 영향을 줄 것을 나타내며, 추후 연구를 통해 모기의 생육정도를 이용한 오염도 측정에 활용이 가능할 것으로 기대된다

다양한 산업분야에서 중금속의 사용이 증가할수록, 중금속으로 인한 환경오염과 생물학적 위해성에 대한 우려의 목소리가 커지고 있다. 통계 지수는 배경농도 값과의 비교를 통해 중금속 오염농도를 정규화 시킴으로써 토양 오염의 정도를 수치화하고, 단계 별로 오염 정도를 판단 할 수 있어 많이 사용된다. 본 연구에서는 농축인자(Enrichment factor, EF), 축적 계수(accumulation index), 잠재적 생물학적 위험 지표(potential ecological risk index)등을 이용하여 중공업 근처 토양 내 중금속 오염가능성을 평가하였다. 연구결과, 중금속의 오염 정도는 정부 가이드라인에 비하여 낮은 수준이었으나, 특정 위치에서 아연, 구리, 납 등의 중금속 오염이 관찰 되었다. 농축인자, 축적계수, 생물학적 위험 지표를 통해 일부 토양 내 중금속 오염이 우려할 수준이며, 주변에 존재하는 인위적 오염원에 의한 오염가능성이 있음을 확인하였다. 연구대상지의 추가 시료채취 및 추정되는 오염원의 시료 확보 후, 동위원소 분석 및 x-ray 기반 분석을 통해 오염원 추적연구가 필요할 것으로 판단된다.

The present polymer have a conjugated polymer backbone system with the designed substituents. The photoluminescence peak of polymer was observed at 525nm, which is corresponded to the photon energy of 2.36 eV and the band gap of poly(EBA) was 2.38 eV. The cyclovoltamograms of the polymer exhibited the irreversible electrochemical behaviors. It was found that the kinetics of the redox process of this conjugated polymer might be mainly controlled by the diffusion process from the experiment of the oxidation current density of polymer versus the scan rate.

We developed a facile methodology for fabricating a free-standing mixed-matrix membrane (MMM) containing covalently incorporated vinyl-functionalized UiO-66-CH=CH2 particles up to 60 wt% by utilizing thiol-ene photopolymerization. FTIR, TGA, SEM, EDX, and XRD strongly supported the fact that the desired MMM containing well-dispersed UiO-66-CH=CH2 particles was successfully produced by C–S bond formation. The MMM was highly flexible and showed improved mechanical properties compared to the pristine polymeric membrane, indicating that the covalently immobilized UiO-66-CH=CH2 particles were homogeneously distributed in the polymer matrix. Gas permeability across the MMM was significantly enhanced compared with the pristine polymeric membrane as diffusion of the gas molecules was facilitated in the porous space of the MOF.

Metallic tantalum powder is manufactured by reducing tantalum oxide (Ta2O5) with magnesium gas at 1,073–1,223 K in a reactor under argon gas. The high thermodynamic stability of magnesium oxide makes the reduction reaction from tantalum oxide into tantalum powder possible. The microstructure after the reduction reaction has the form of a mixture of tantalum and magnesium oxide, and the latter could be entirely eliminated by dissolving in weak hydrochloric acid. The powder size in SEM microstructure for the tantalum powder increases after acid leaching in the range of 50–300 nm, and its internal crystallite sizes are observed to be 11.5 to 24.7 nm with increasing reduction temperatures. Moreover, the optimized reduction temperature is found to be 1,173 K as the minimum oxygen concentration is approximately 1.3 wt.%.

배경목적: 내시경 초음파 유도하 췌장 저류액 배액은 효과적인 시술이나 이 시술에 특화된 맞춤형 부속기구는 부족한 실정이다. 이 연구의 목적은 내시경 초음파 유도하 경위장관 배액술 전용으로 새로 고안된 양측 플랜지가 있는 완전피막형 금속 스텐트의 유용성을 평가하고자 하였다. 방법: 동물연구는 한 마리의 개를 대상으로 하였고 임상연는 췌장 저류액을 가진 5명의 환자 (5명은 췌장가성낭종, 1명은 벽 형성 췌장괴사)를 대상으로 하여 내시경 초음파 유도하 배액술을 시행하였다. 연구의 성과는 기술적, 임상적 성공여부, 합병증, 스텐트 제거 가능 여부로 판단하였다. 결과: 동물연구에서 스텐트는 내시경 초음파 유도하 경십이지장 접근으로 합병증 없이 성공적으로 유치되었다. 시술 직후 시행한 부검에서 담낭-십이지장 연결은 온전하였다. 6명의 환자에서 모두 스텐트는 성공적으로 유치되었다. 모든 환자에서 시술후 합병증과 스텐트 이탈은 없었다. 결론: 새로 고안된 양측 플랜지가 있는 완전피막형 금속스텐트를 사용한 췌장저류액의 내시경 초음파 유도하 경위장관 배액술은 기술적으로 가능하였고 심각한 합병증은 없었다. 스텐트 선단부의 맞춤형 플랜지 형상은 시술의 효과를 배가시켰다.

Nitrogen is a serious contaminant in natural gas because it decreases the energy density. The natural gas specification in South Korea requires a N2 content of less than 1 mol%. Thus, cost-effective N2 removal technology from natural gas is necessary, but until now the only option has been energy-intensive processes, e.g., cryogenic distillation. Using porous materials for the removal process would be beneficial for an efficient separation of CH4/N2 mixtures, but this still remains one of the challenges in modern separation technology due to the very similar size of the components. Among various porous materials, metal-organic frameworks (MOFs) present a promising candidate for the potential CH4/N2 separation material due to their unique structural flexibility. A MIL-53(Al), the most well-known flexible metal-organic framework, creates dynamic changes with closed pore (cp) transitions to open pores (ops), also called the ‘breathing’ phenomenon. We demonstrate the separation performance of CH4/N2 mixtures of MIL-53(Al) and its derivative MIL-53-NH2. The CH4/N2 selectivity of MIL- 53-NH2 is higher than pristine MIL-53(Al), suggesting a stronger CH4 interaction with NH2.

Cu(II) can cause health problem for human being and phosphate is a key pollutant induces eutrophication in rivers and ponds. To remove of Cu(II) and phosphate from solution, chitosan as adsorbent was chosen and used as a form of hydrogel bead. Due to the chemical instability of hydrogel chitosan bead (HCB), the crosslinked HCB by glutaraldehyde (GA) was prepared (HCB-G). HCB-G maintained the spherical bead type at 1% HCl without a loss of chitosan. A variety of batch experiment tests were carried out to determine the removal efficiency (%), maximum uptake (Q, mg/g), and reaction rate. In the single presence of Cu(II) or phosphate, the removal efficiency was obtained to 17 and 16%, respectively. However, the removal efficiency of Cu(II) and phosphate was increased to 50~55% at a mixed solution. The maximum uptake (Q) for Cu(II) and phosphate was enhanced from 11.3 to74.4 mg/g and from 3.34 to 36.6 mg/g, respectively. While the reaction rate of Cu(II) and phosphate was almost finished within 24 and 6 h at single solution, it was not changed for Cu(II) but was retarded for phosphate at mixed solution.