Heavy metals in stream water and sediments around industrial complex were studied in order to assess the contamination and to identify the potential source of metals. High variability has been observed for both dissolved and particulate phases in stream water with coefficient of variation (CV) ranging from 1.3 to 2.8. The highest metal concentrations in both phases were observed in Gunja for Ni and Cu, in Jungwang for Zn and Pb and in Shiheung for Cd, respectively. These results indicate that the different metal sources could be existing. The concentrations of the heavy metals in sediments decreased in the order of Cu>Zn>Pb>Cr>Ni>As>Cd>Hg, with mean of 2,549, 1,742, 808, 539, 163, 17.1, 5.8, 0.07 mg kg-1, respectively. Mean of metal concentrations (except for As) in sediments showed the highest values at Shiheung stream comparing with other streams. In sediments, the percent exceedance of class II grade that metal may potentially harmful impact on benthic organism for Cr, Ni, Cu, Zn, Cd, Pb was about 57%, 62%, 84%, 60%, 68%, 81% for all stream sediments, respectively. Sediments were classified as heavily to extremely polluted for Cu and Cd, heavily polluted for Zn and Pb, based on the calculation of Igeo value. About 59% and 35% of sediments were in the categories of “poor” and “very poor” pollution status for heavy metals. Given the high metal concentrations, industrial wastes and effluents, having high concentrations of most metals originated from the manufacture and use of metal products in this region, might be discharged into the stream through sewer outlet. The streams receive significant amounts of industrial waste from the industrial facilities which is characterized by light industrial complexes of approximately 17,000 facilities. Thus, the transport of metal loads through streams is an important pathway for metal pollution in Shihwa Lake.

파이로프로세싱의 전해환원공정에서 생산된 금속전환체의 조성은 전해정련공정 운전의 중요한 운전변수인 용융염 중 UCl3 의 농도변화에 영향을 미친다. 따라서, 본 연구에서는 금속전환체에 함유된 TRU와 RE 원소의 함량 및 금속전환체에 동반 되어 전해정련 전해조에 유입될 수 있는 Li2O 농도가 전해정련 전해조의 UCl3 농도 변화에 미치는 영향을 검토하였다. 금속 전환체의 TRU 원소와 RE 원소의 농도만을 고려하였을 때 전해정련 운전 batch 수 증가에 따라 UCl3 농도가 감소하였다. 전 해정련 1 campaign(20 batch)를 운전하기 위해서는 UCl3를 3회 이상 추가 보충해야 함을 알 수 있었다. 한편, 금속전환체에 동반되어 전해정련 전해조에 유입되는 Li2O의 유입량 증가에 따라 UCl3 농도 감소의 영향이 크게 나타났으며, 이에 따라 운전 가능 batch 수가 급격히 감소하게 되어 전해정련 운전에 중요한 운전 변수임을 보여주었다. 이러한 결과는 전해정련 운전 중 UCl3 농도 유지를 위해 금속전환체에 포함된 TRU 및 RE 원소뿐만 아니라 금속전환체에 동반되어 유입될 가능성이 있는 Li2O의 영향도 고려하여 전해정련 운전모드를 설정하여야 함을 보여주었다.

본 연구는 인삼과 산양삼의 부위별 중금속 분포양상을 조사하여 중금속 식이노출 저감화 방안을 모색하고자 하였다. 인삼과 산양삼은 지역별 배분을 통해 각각 14개 지역 및 5개 지역에서 시료를 채취하였으며, 각 부위별 중량 및 중금속 함량을 분석하였다. 중금속 분석을 위해 microwave 장치를 이용해 전처리한 후 납, 카드뮴 및 비소는 ICP-MS로 측정하고 알루미늄은 ICP를 이용한 분석법을 확립하였다. 인삼의 겉껍질은 전체의 16.2% 중량비를 차지하였으며, 산양삼의 겉껍질 및 잔뿌리는 각각 전체의 21.8%, 16.8%의 중량비를 차지하였다. 각 부위별 중량비와 중금속 농도를 고려하여 각 부위별 중금속 분포도를 산출하였다. 인삼 및 산양삼의 겉껍질은 전체에 차지하는 중량비에 비해 높은 중금속 함유량을 보이고 있었으며, 인삼의 경우 납의 40.3%, 카드뮴 25.9%, 비소 47.6%, 알루미늄 89.9%가 겉껍질에 잔존하고 있었으며 산양삼의 경우 납 27.2%, 카드뮴 28.2%, 비소 48.3%, 알루미늄 56.8%가 겉껍질에 존재하였다. 알루미늄을 제외하고 산양삼의 잔뿌리내 중금속 분포량은 겉껍질과 유의적 차이가 없었다. 따라서, 인삼 및 산양삼의 겉껍질을 벗기고 섭취 한다면 중금속 식이노출량을 크게 줄일 수 있음을 확인하였다.

The physical treatment such as chemical precipitation or adsorption was usually added after biological treatment in wastewater treatment process since it was enforced to reduce the concentration of phosphate for wastewater effluent to 0.2 mg/L as P which was well known as one of main nutrient causing eutrophication in waterbody. Therefore, the new material functioned for both adsorption and disinfection was prepared with Fe and Cu, and TiO2, respectively, by changing the ratio of concentration referred to tri-metal (TM). According to SEM-EDS, TiO2 was 30~40% composition for any TM regardless of any synthesis condition. However, the ratio of composition for Fe and Cu was dependent on the initial Fe and Cu concentration, respectively. The removal efficiency of phosphate was obtained to 15% at low initial concentration and the maximum uptake (Q) was calculated to ~11 mg/g through Langmuir isotherm model using TM1 which was synthesized at 1000 mg/L, 1000 mg/L, and 2 g (10 g/L) for Fe(NO3)3, Cu(NO3)2, TiO2, respectively. In disinfection test, the efficiency of virus removal using TM was increased with increase of dosage of TM and can be reached 98% at 0.2 g.

The recent development of information and communication technologies brings new changes to automobile traffic systems. The most typical example is the advancement of dedicated short range communication(DSRC). DSRC mainly consists of an intelligent transportation system(ITS), an electronic toll collection system(ETCS) and an advanced traveler information system(ATIS). These wireless communications often cause unnecessary electromagnetic waves, and these electromagnetic waves, in turn, cause frequent system malfunction. To solve this problem, an absorber of electromagnetic waves is suggested. In this research, various materials, such as powdered metal and iron oxides, are used to test the possibility for an effective absorption of the unnecessary electromagnetic waves. The various metal powders are made into a thin sheet form by compositing through processing. The electromagnetic characteristics(complex permittivity, complex permeability) of the fabricated sheet are measured. As a result, we achieve –6.5 dB at 940 MHz(77.6 % absorption rate) with a 1.0 mm-thickness electromagnet wave absorber, and –9.5 dB at 940 MHz(88.8 % absorption rate) with a 2.0 mm-thickness absorber.

가속화되는 산업화로 인해 중금속 이온의 침출이 환경문제로 떠오르고 있다. 수질 정화를 위한 몇 가지 방법 중 기능성 고분자 섬유를 이용한 흡착은 효율적이며 경제적이라는 장점이 있다. 특히, 폴리아크릴로나이트릴(polyacrylonitrile, PAN)은 금속 이온을 흡착할 수 있는 작용기가 많아 관심을 끌고 있다. PAN은 쉽게 전기방사를 통해 고분자 나노 섬유화될 수 있으며 높은 표면적을 가질 수 있다. 본 총설에서 다룰 복합 PAN 섬유는 폐수 처리를 위한 또 다른 유형의 고분자이다.

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 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.

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.

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.