Organic-inorganic hybrid coating films have been used to increase the transmittance and enhance the physical properties of plastic substrates. Sol-gel organic-inorganic thin films were fabricated on polymethylmethacrylate (PMMA) substrates using a dip coater. Metal alkoxide precursor tetraethylsilicate (TEOS) and alkoxy silanes including decyltrimethoxysilane (DTMS), 3-glycidoxypropyltrimethoxysilane (GPTMS), phenyltrimethoxysilane (PTMS), 3-(trimethoxysilyl)propyl methacrylate (TMSPM) and vinyltrimethoxysilane (VTMS) were used to synthesize sol-gel hybrid coating solutions. Sol-gel synthesis was confirmed by the results of FT-IR. Cross-linking of the Si-O-Si network during synthesis of the sol-gel reaction was confirmed. The effects of each alkoxy silane on the coating film properties were investigated. All of the organicinorganic hybrid coatings showed improved transmittance of over 90 %. The surface hardness of all coating films on the PMMA substrate was measured to be 4H or higher and the average thickness of the coating films was measured to be about 500 nm. Notably, the TEOS/DTMS coating film showed excellent hydrophobic properties, of about 97°.
Various types of solidifying materials are used to stabilize and solidify low and intermediatelevel radioactive dispersible waste. Portland cement is generally used to solidify various radioactive wastes because its facilities and processes are simple, less dangerous, and it has excellent compressive strength after curing compared to other materials. However, it is difficult to use Portland cement in radioactive waste containing highly water-soluble harmful substances such as sodium fluoride because it is prone to leaching harmful ingredients in immersion tests due to its low water resistance. In this study, solidification was achieved using an organic-inorganic hybrid solidifying binders consisting of inorganic binders such as Portland cement, blast furnace slag powder, silica fume, and organic binders such as epoxy resin. This material was then compared with a solidification material made of Portland cement alone. The mixing ratio of inorganic binders, water, and organic binders to simulated waste is 35%, 20%, and 25%, respectively. The mixing ratio of inorganic binders and water when using only Portland cement for simulated waste is 100% and 80%, respectively. The mixed paste was poured into a cylinder mold (Φ 5 × 10 cm) to seal the upper part, cured at room temperature for 28 days to produce a solidification specimen, and then subjected to various tests were performed, including compressive strength, immersion compressive strength, hydration peak temperature, length change, and immersion weight change. The compressive strength of the organic-inorganic hybrid solidification test was 13-17 MPa, the immersion compressive strength was 15-18 MPa, the hydration peak temperature was 33-36°C, the length change rate was -0.086%, and the immersion weight change rate was –2.359%. The compressive strength of the Inorganic solidification test using only Portland cement was 16-18 MPa, the immersion compressive strength was 20-21 MPa, the hydration peak temperature was 23-25°C, the length change rate was -0.150%, and the immersion weight change rate was -5.213%. The compressive strength and immersion compressive strength of the organic-inorganic hybrid solidification materials were slightly lower compared to those of Portland cement solidification materials, they still met the compressive strength standard of 7-12 MPa, taking into consideration the strength reduce and economic feasibility of the core drill process. Furthermore, it indicates that the rates of change in length and immersion weight decreased to about 1% and 5%, suggesting an improvement in water resistance. The above results suggest that applying the organic-inorganic hybrid solidification method to radioactive waste treatment can effectively improve water resistance and help secure long-term stability.
휘어지며 투명한 전자기기의 개발을 위해서 최근 유기반도체, 탄소기반 나노소재, 금속산화물 반도체등의 다양한 신소재 반도체 개발에 대한 연구가 관심을 받으며 지속적으로 발전하고 있다. 그러나, 이러한 신소재 반도체 기술의 꾸준하고 지속적인 발전에도 불구하고 트랜지스터를 구성하는 주요 소재중 하나인 유전체에 대한 연구는 반도체의 개발속도에 크게 미치지 못하여, 기계적인 휘어짐의 특성을 갖추고, 높은 캐패시턴스와 좋은 누전전류 특성을 갖는 새로운 유전체 개발에 대한 요구가 지속적으로 커지고 있다. 이에 본 연구는 저전압에서 구동 가능한 박막트랜지스터를 위한 유기-무기 하이브리드소재 박막을 개발하며 이를 저전압 구동이 가능한 유기박막트랜지스터에 적용하였다. 상대적으로 높은 유전상수를 갖는 염화하프늄 (HfO2)과 소수성기를 갖고 있으며 금속산화물과 공유결합이 가능한 실란산 기반의 유기물 (octadecyltrimethoxysilane)을 혼합한 전구체 용액을 합성하며 상대적으로 낮은 온도에서 열처리를 통해 얻을 수 있었다. 제조된 하이브리드 게이트 유전체 박막은 우수한 절연 및 유전체 특성과 함께 소수성 표면 특성을 가질 수 있었고 펜타센 유기박막트랜지스터로 응용하여 저전압에서 구동이 되며 우수한 트랜지스터 성능을 갖는 소자를 개발하였다.
Metal halide perovskite nanocrystals, due to their high absorption coefficient, high diffusion length, and photoluminescence quantum yield, have received significant attention in the fields of optoelectronic applications such as highly efficient photovoltaic cells and narrow-line-width light emitting diodes. Their energy band structure can be controlled via chemical exchange of the halide anion or monovalent cations in the perovskite nanocrystals. Recently, it has been demonstrated that chemical exfoliation of the halide perovskite crystal structure can be achieved by addition of organic ligands such as noctylamine during the synthetic process. In this study, we systematically investigated the quantum confinement effect of methylammonium lead bromide (CH3NH3PbBr3, MAPbBr3) nanocrystals by precise control of the crystal thickness via chemical exfoliation using n-octylammonium bromide (OABr). We found that the crystalline thickness consistently decreases with increasing amounts of OABr, which has a larger ionic radius than that of CH3NH3 + ions. In particular, a significant quantum confinement effect is observed when the amounts of OABr are higher than 60 %, which exhibited a blue-shifted PL emission (~ 100 nm) as well as an increase of energy bandgap (~ 1.53 eV).
본 연구에서는 와편모조류 Alexandrium affine(LIMS-PS-2345)의 생장에 미치는 용존태 무기 및 유기 영양염의 영향을 조사하였 다. 영양염 흡수 동력학 실험에서 A. affine의 최대흡수속도(ρmax)와 반포화상수(Ks)는 질산염에서 77.0 pmol/cell/hr과 17.6 μM, 인산염에서 15.5 pmol/cell/hr과 3.88 μM로 산출되어, 무기영양염에 대하여 높은 요구량 및 낮은 친화성을 가지고 있는 것으로 나타났다. 유기 영양염에 따른 A. affine의 생장속도를 확인한 결과, 유기 질소 urea, glycine와 유기 인 adenosine triphosphate(ATP), glycerol phosphate(Glycerol-P) 첨가구에서 무기 영양염 첨가구의 70 % 이상 생장속도를 보였다. 따라서 낮은 무기 영양염 환경에서 A. affine의 우점화와 종간경쟁에서 우위를 위해서는 용존태 유기 영양염의 이용이 필요할 것으로 생각된다.
Using UV nanoimprint lithography(UV-NIL), 1-dimensional(1-D) pattern structures were fabricated on a hybrid mixture thin film of lanthanum oxide and a UV-curable resin. 1-D pattern on a wafer fabricated by the laser interference lithography was transferred to polydimethylsiloxane and this is used as a mold of UV-NIL process. Conducting an X-ray photoelectron spectroscopy, C 1s and La 3d spectra were analyzed, and it was confirmed that hybrid thin film was successfully deposited on glass substrate. Also, transferred pattern structure was observed by using an atomic force microscopy. Through this, it was revealed that agglomerations between 1-D pattern were increased as UV irradiation time increased and this phenomenon disrupted the quality of NIL process. Additionally, liquid crystal(LC) cells with patterned hybrid thin films were fabricated and LC alignment performances were investigated. Using the polarizing optical microscopy and the crystal rotation method, LC alignment state and pretilt angles were observed. Consequently, the uniform homogeneous LC alignment was achieved at UV irradiation time of 1min and 3min where high resolution pattern transfer was observed.
토양검정에 의한 유기자원 시비처방 효과를 구명하기 위하여 유기자원의 질소, 인산, 칼륨 성분 함량에 무기화율을 적용하여 시비량을 설정하고 골든퀸 벼를 대상으로 포장시험을 실시하였다. 1. 초장, 분얼수, 엽색도와 이삭수, 볏짚수량 및 벼 수량은 유기자원과 화학비료처리간 차이가 없었다. 등숙율은 화학비료구에서 가장 낮았으며, 천립중은 무처리구에서 가장 높았다. 2. 현미쌀의 미량원소 중 철은 시비구에서 높았고, 아연은 유기자원구에서 가장 높았으며, 무처리구에서 가장 낮았다. 3. 수확 후 토양화학성 중 산도는 화학비료구에서 높았다. 칼슘과 마그네슘은 시비구에서 높았고, 유효규산함량은 유기자원>화학비료>무처리 순으로 높았다. 4. 벼 수량과 양(+)의 상관이 인정된 토양 화학성은 칼슘, 마그네슘과 유효규산 함량이며, 수량 구성요소로는 이삭수였다. 등숙율과 천립중은 음(-)의 상관이 인정되었다. 벼 수량과 가장 높은 상관을 보인 이삭수(r=0.98)는 토양 칼슘, 마그네슘 및 토양 유효규산과 양(+)의 상관이었다. 5. 화학비료를 대체하기 위하여 토양검정 후 유기자원에 무기화율을 적용하여 시비처방을 한 결과 벼 생육, 볏짚 및 벼 수량에서 유기자원구와 화학비료구의 차이가 없었으며, 현미 쌀의 아연성분과 토양 유효규산함량은 유기자원구에서 더 높아 유기자원으로 화학비료를 대체할 수 있다.
Biological phosphorus removal is accomplished by exposing PAO(phosphorus accumulating organisms) to anaerobic-aerobic conversion conditions. In the anaerobic condition, PAO synthesize PHB(polyhydroxybutyrate) and simultaneously hydrolysis of poly-p resulting phosphorus(Pi) release. In aerobic condition, PAO uptake phosphorus(Pi) more than they have released. In this study, cyanobacteria Synechococcus sp., which is known to be able to synthesize PHB like PAO, was exposed to anaerobic-aerobic conversion. If Synechococcus sp. can remove excess phosphorus by the same mechanism as PAO, synergistic effects can occur through photosynthesis. Moreover, Synechococcus sp. is known to be capable of synthesizing PHB using inorganic carbon as well as organic carbon, so even if the available capacity of organic carbon decreases, it was expected to show stable phosphorus removal efficiency. In 6 hours of anaerobic condition, phosphorus release occurred in both inorganic and organic carbon conditions but SPRR(specific phosphorus release rate) of both conditions was 10 mg-P/g-MLSS/day, which was significantly lower than that of PAO. When converting to aerobic conditions, SPUR(specific phosphorus uptake rate) was about 9 mg-P/g-MLSS/day in both conditions, showing a higher uptake rate than the control condition showing SPUR of 6.4 mg-P/g-MLSS/day. But there was no difference in terms of the total amount of removal. According to this study, at least, it seems to be inappropriate to apply Synechococcus sp. to luxury uptake process for phosphorus removal.
Organic-inorganic hybrid perovskite nanocrystals have attracted a lot of attention owing to their excellent optical properties such as high absorption coefficient, high diffusion length, and photoluminescence quantum yield in optoelectronic applications. Despite the many advantages of optoelectronic materials, understanding on how these materials interact with their environments is still lacking. In this study, the fluorescence properties of methylammonium lead bromide (CH3NH3PbBr3, MAPbBr3) nanoparticles are investigated for the detection of volatile organic compounds (VOCs) and aliphatic amines (monoethylamine, diethylamine, and trimethylamine). In particular, colloidal MAPbBr3 nanoparticles demonstrate a high selectivity in response to diethylamine, in which a significant photoluminescence (PL) quenching (~ 100%) is observed at a concentration of 100 ppm. This selectivity to the aliphatic amines may originate from the relative size of the amine molecules that must be accommodated in the perovskite crystals structure with a narrow range of tolerance factor. Sensitive PL response of MAPbBr3 nanocrystals suggests a simple and effective strategy for colorimetric and fluorescence sensing of aliphatic amines in organic solution phase.
본 연구에서는 가압식 분리막 여과에서 무기입자의 존재가 유기파울링에 미치는 영향을 관찰하였다. 유기파울링의 유발을 위해 알긴산나트륨(sodium alginate, SA)를 이용한 정밀여과 실험에서 무기 실리카(SiO2) 입자의 존재 유무와 상관 없이 분리막 파울링은 여과초기 완전공극막힘에서 여과시간이 경과할수록 케이크 형성에 의해 주로 지배되었다. 그러나 무기 입자의 존재 시 정압여과에서 알긴산나트륨 파울링 케이크 비저항값과 압축성은 상대적으로 낮게 관찰되었고 이로 인해 낮은 파울링 속도가 관찰되었다. 동일한 시료를 이용한 정량여과 실험을 수행한 결과 정압여과에 비해 정량여과에서 여과초기 공극막힘현상 및 파울링 속도는 더욱 증가하였다. 이와 같은 현상은 파울링층이 지닌 압축성으로 막간차압의 증가 시 케이크 비저항값이 함께 증가하였기 때문인 것으로 판단된다. 알긴산나트륨과 실리카 입자가 함께 존재 시 알긴산나트륨이 단독으로 존재하는 것보다 수리학적 세정을 통한 파울링 제거효과는 더욱 좋은 것으로 관찰되었다.