The goal of this study is to propose the effective method of investigating the injurious factors and making improved plans that prevents the workers against musculoskeletal disorders at an autopart company and the same business field with similar working conditions and process. A questionnaire were adopted to analyze the symptoms of workers' musculoskeletal disorders, and an ergonomic assessment method such as QEC, RULA, S.I were performed to find out harmful factors of workplace and working posture. Based on the result of the evaluation, to enhance the working environment, improvement of worktable, working space, tools, and outfit was suggested, and induction of mechanical system was also suggested. It can be concluded that the method and process described in this paper could be helpful for diagnosing the musculoskeletal disorders and making improvement plans to the autopart company and the same business field with similar working conditions and process.

The alumina nano powders synthesized by levitational gas condensation (LGC) method were applied to catalyst in manufacturing process of Hanzsch reaction for Nitrendipine. The L-tartaric acid on the surface is carried out with participation of carbonyl fragments, O-H, C-H bonds which affects stereo selectivity, yield on the reagents positively. From the analysis of the IR-spectroscopy, the carbonyl fragments, O-H, and C-H bond were created by the catalytic reaction. From the analysis of the rR-spectroscopy, the carbonyl fragments, O-H, and C-H bond were created by the catalytic reaction. The newly created bonds made a chiral center on the final product.

It is well known that thermal plasma process has lots of advantages such as high temperature and good quality for synthesis of nano particles. In this research, we attempt the synthesis of nano unitary and composite powder (Ag, Mg-Al, Zr-V-Fe) using transferred thermal plasma. Nano particles of metal alloy, ranging from 20 nm to 150 nm, have been synthesized by this process.

Cu-Ni-P alloy nano powders were fabricated by the electrical explosion of electroless Ni plated Cu wires. The effect of applied voltage on the explosion was examined by applying pulse voltage of 6 and 28 kV, The estimated overheating factor, K, were 1.3 for 6 kV and 2.2 for 28 kV. The powders produced with pulse voltage of 6 kV were composed of Cu-rich solid solution, Ni-rich solid solution, and phase. While, those produced with 28 kV were complete Cu-Ni-P solid solution and small amount of phase. The initial P content of 6.5 at.% was reduced to 2-3 at.% during explosion due to its high vapour pressure.

Ultrasonic-milling of metal oxide nanopowders for the preparation of tungsten heavy alloys was investigated. Milling time was selected as a major process variable. XRD results of metal oxide nanopowders ultrasonic-milled for 50 h and 100 h showed that agglomerate size reduced with increasing milling time and there was no evidence of contamination or change of composition by impurities. It was found that nanocomposite powders reduced at in a hydrogen atmosphere showed a chemical composition of 93.1W-4.9Ni-2.0Fe from EDS analysis. Hardness of sintered part using 50 h and 100 h powder samples was 399 Hv and 463 Hv, respectively, which is higher than the that of commercial products (330-340 Hv).

The magnetic alloys of Cu-Fe () were prepared by a mechanical alloying method and their structural and magnetic behaviors were examined by X-ray diffraction and Mossbauer spectra. The magnetization curves did not distinctly show the saturation at 70 kOe for the concentrated alloys of . The Mossbauer spectrum of at room temperature shows one Lorentzian line of the paramagnetic phase, whereas the Mossbauer spectrum of consists of sextet Lorentzian line at room temperature and a centered doublet line. The Mossbauer spectra of measured in the temperature ranges from 13 to 295 K, implies that to consists of two magnetic phases. One superimposed sextet corresponds to the ferromagnetic iron in Cu and the other one indicates the superparamagnetic iron rich phase.

SPG (Shirasu porous glass) 관형 막이 설치된 회분식 막유화 장치를 사용하여 이온성 약물이 담지된 단분산 polycaprolactone (PCL) 마이크로캡슐을 제조하기 위한 막유화 공정변수의 최적조건을 결정하였다. 마이크로캡슐에 담지된 이온성 약물로는 양이온성인 lidocaine-hydrochloride, 중성인 sodium salicylate와 음이온성인 4-acetaminophen의 3가지를 사용하였으며, PCL 마이크로캡슐로부터 이들 모델약물의 방출거동을 검토하였다. 캡슐제조에 사용된 PCL의 농도와 분자량, 막간 압력차, 분산상과 연속상에 첨가시킨 유화제의 농도, 연속상의 교반속도가 막유화법으로 제조된 PCL 캡슐의 크기와 크기분포에 미치는 영향을 검토하였다. 이들 공정변수의 조절을 통해 평균 크기 약 5 μm의 균일한 마이크로캡슐을 제조할 수 있었다. 약물 방출실험 결과 산성조건에서 알칼리조건으로 방출환경이 변화됨에 따라 약물 방출속도가 증가하였다.

Methane combustion over perovskite catalysts was investigated. For the preparation of catalysts, Co, Mn, Fe, and Ni were used as B-site components of the perovskite catalysts (ABO3) and La was used as A-site component. The effect of calcination temperature on methane combustion and perovskite structure was also investigated. The structure of perovskites, surface area, and adsorbed oxygen species were tested with XRD, BET apparatus, and O2-TPD, respectively. The formation of perovskite structure was affected by the calcination temperature. The catalyst desorbing oxygen at a lower temperature showed better activity for the methane combustion, therefore, the oxygen species desorbing at lower temperatures is responsible for the methane combustion.

본 연구에서는 나노여과막과 역삼투막의 표면 개질을 통하여 유량의 향상 및 내오염성을 향상시키는 제조 방법을 개발하였다. 실란 화합물이 코팅된 복합막의 표면 성질이 막 오염 지수 MFI 값에 미치는 영향을 살펴보았다. 상용화된 역삼투막(RE1812-LP)과 나노여과막(ESNA 4040-LF) 복합막을 기저막으로 사용하여 실란 커플링제의 농도를 달리하여 개질 복합막을 제조하였다. 실란 커플링제 aminopropylmethoxydiethoxysilane은 아민 관능기와 3개의 알콕시 관능기를 가지며 아민 관능기가 가지는 친수성 특성이 개질막의 투과 수량 및 내오염성에 미치는 영향을 조사하였다. 개질막의 실란층의 안정적인 형성을 확인하기 위하여 FE-SEM, 접촉각 측정 및 제타 전위값 등의 표면 특성 변화를 살펴보았다. 특히 개질된 나노여과막의 2가 이온 수용액을 공급수로 할 경우 염제거율에 대한 영향 없이 내오염성이 현저히 증가함을 확인하였다.

당뇨병 환자의 혈당치 측정을 위하여 폴리우레탄으로 만들어진 진단막을 제조하였다. 플라즈마와 혈액속의 글루코오즈의 농도를 변화시켜가며 활성화된 폴리우레탄 진단막을 가지고 680 nm에서의 최종흡광도를 측정하였다. 여러 가지 보관온도에서 3일, 1주, 3주, 5주간 보관 후 온도가 글루코오즈의 농도 측정에 미치는 영향을 조사하였다. 우레탄 진단막의 안정성을 상대습도 80%에서 측정하였다.

Polyethersulfone (PES)와 Bovine Serum Albumin (BSA) 용액으로 전기방사법을 이용하여 단백질 친화막을 제조하였다. 방사운전조건(방사용액의 농도, 전압, 방사속도, 방사거리)을 다양하게 조절하여 나노섬유의 크기를 관찰하였으며, 최적의 친화막 제조 조건을 확인할 수 있었다. XPS와 FT-IR로써 PES와 BSA의 결합을 확인하였으며, PES-BSA 나노섬유의 최적 방사 온도와 습도는 20~22℃와 45~55% 임을 알 수 있었다. 또한 PES 함량이 증가할수록 섬유의 크기가 증가하고, BSA의 경우 나노섬유의 크기에 큰 영향이 없음을 알았다. PES 7 wt%, BSA 0.7 wt%. Hexafluropropanol (HFP) 92.3 wt%의 용액을 이용하여 전압 10.0 kV, 방사거리 10 cm, 방사속도 1.0 mL/hr의 조건에서 방사한 경우 균일한 크기의 PES-BSA 나노섬유가 얻어졌다.