혈액 속에 있는 글루코우즈의 농도를 측정하기 위해 폴리아크릴로니트릴로 만들어진 진단막을 제조하였다. 혈액속의 글루코우즈의 농도를 변화시켜 가며 폴리아크릴로니트릴 진단막을 가지고 680nm에서의 최종흡광도를 측정하였다. 시간에 따른 흡광도 변화량(K/S)의 최종결과치가 글루코우즈의 농도가 증가함에 따라 직선적으로 증가함을 알 수 있었다. 혈액 속에 존재할 가능성이 있는 화합물들이 글루코우즈의 농도측정에 미치는 영향을 조사하였다. 그 결과 대부분의 화합물들이 글루코우즈의 농도측정에 큰 영향을 미치지 않는 것을 알 수 있었다.

Poly(vinyl chloride) (PVC) 주사슬과 poly(hydroxyethyl acrylate) (PHEA) 곁사슬로 구성된 가지형 공중합체를 원자전달라디칼 중합을 통해 합성하였다. PVC의 2차 염소원자의 직접적인 개시반응에 의해 친수성인 PHEA 단량체를 그래프팅시켰다. 이렇게 합성된 PVC-g-PHEA을 술포석시닉산(SA)를 사용하여 가교시켰으며, 이는 가지형 공중합체의 -OH 그룹과 SA의 -COOH와의 에스테르 반응임을 FT-IR 분광법을 이용하여 분석하였다. 이온교환능(IEC)은 SA 함량이 증가함에 따라 계속하여 증가하여 0.87 meq/g까지 도달하였고, 이는 전해질막에 이온 그룹수가 증가하기 때문이다. 하지만, 함수 율은 SA 함량이 20 wt%까지는 증가하다 그 이상에서는 감소하였다. 또한 수소 이온 전도도도 SA 함량에 따라 증가하여 20 wt% SA 농도에서 0.025 S/cm의 최대값을 나타내었고, 이는 SA 함량이 증가함에 따라 이온 그룹의 수가 증가하는 효과와 가교가 증가하는 효과가 서로 경쟁적으로 일어나기 때문으로 사료된다.

High-pressure abrasive entrained jet have rapidly become important machining technology over the last two decades. However, suspension jet by high-pressure has been recently developed for packaging sawing. Ideally, diamond materials should be used for components in abrasive water-jet systems that are subject to high erosive conditions. Using the diamond orifices improve maintenance and extend wear part life. This paper gives insights to using an abrasive suspension jet with diamond orifice. The influences of orifice material and orifice design are evaluated.

Formation and characteristics of spraying powder for BSCCO High-Tc superconductor prepared by plasma spray coating were investigated. The addition of 3% of binder gives the best flowability of the powder. Ball milling for 30h and 35h gives the best flowability of powder in the case of 2001 and 0212, respectively. The withdraw ratio increases upon binder addition from 12 to 27% in the case of 2001 and from 18 to 31% in the case of 0212 for sieving powder of in size. The built-up efficiency for thickness of spray coating is increased more than 30% by binder addition. The microstructure of the spray coated layers was investigated by XRD and EDS analysis.

Oil-based nanofluids were prepared by dispersing Ag, graphite and carbon black nanoparticles in lubricating oil. Agglomerated nanoparticles were dispersed evenly with a high-speed bead mill and/or ultrasonic homogenizer, and the surfaces of the nanoparticles were modified simultaneously with several dispersants. Their tribological behaviors were evaluated with a pin-on-disk, disk-on-disk and four-ball EP and wear tester. It is obvious that the optimal combination of nanoparticles, surfactants and surface modification process is very important for the dispersity of nanofluids, and it eventually affects the tribological properties as a controlling factor. Results indicate that a relatively larger size and higher concentration of nanoparticles lead to better load-carrying capacity. In contrast, the use of a smaller size and lower concentration of particles is recommended for reducing the friction coefficient of lubricating oil. Moreover, nanofluids with mixed nanoparticles of Ag and graphite are more suitable for the improvement of load-carrying capacity and antiwear properties.

본 연구에서는 소비자들이 선호하는 휴대폰 제조사 브랜드를 평가하기 위하여 무형 자산 평가기법을 적용하여 비교 분석 하였다. 기존의 연구는 기초적인 통계적 사실에 근거하여 단편적으로 평가를 하였다. 하지만 휴대폰 제조사 선호도 평가는 무형자산 평가와 깊은 관련이 있다. 따라서 본 연구에서는 기존 연구와는 다르게 무형자산 평가기법을 적용하여 휴대폰 제조사 브랜드 선호도를 평가하고자 한다.

Nanostructured carbon materials have been found to have applications in fuel cell electrodes, field emitters, electronic devices, sensors and electromagnetic absorbers, etc. Especially, the CNF (carbon nanofiber) can be expected to play an important role in catalyst supporters for fuel cell electrodes and chemical reactions. In this study, we synthesized CNF from a liquid phase carbon source by a solvothermal method. In addition, we studied the parameters for the preparation of CNF by controlling heating and cooling rates, synthesis temperature and time. We characterized the CNF by SEM/TEM, XRD, Raman spectroscopy and EDS. We found that the heating and cooling rate have strong effects on the CNF formation and growth. We were able to prepare the best CNF at the heating rate of 10˚/min, at 450˚ for 60 minutes, and at the cooling rate of 4˚/min. As a result of Raman spectra, we found that the sample showed two characteristic Raman bands at ~1350cm-1 (D band) and ~1600cm-1 (G band). The G band indicates the original graphite feature, but the D band has been explained as a disorder feature of the carbon structure. The diameter and length of the CNF was about 15~20nm, and over 1μ, respectively.