• 한국산학기술학회논문지
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• 제17권4호
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• pp.100-105
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• 2016

3D 프린터의 증가에 따라 대량 생산이 아닌 소량 제품의 빠른 개발 시간을 고려하여 3D 스캐너의 활용도 점차 증가하고 있다. 소량 생산 개발 트렌드뿐만 아니라 최근 자동차 및 전자부품의 제조업에 있어서도 정밀 부품의 개발 및 검사, 측정 등의 품질 문제가 중요한 이슈로 떠오르고 있다. 최근 3D 스캐너 장비 효율성 및 인식기술은 지속적으로 향상되었지만, 이에 반해, 이를 준비하는 스프레이 작업은 시간이 많이 걸리고 환경문제가 유발되기 때문에 제조업 제품 개발자들은 자동스프레이 도포 시스템 개발에 대해 지속적으로 요구해 왔다. 본 연구를 통해서 3D 스캔 준비 작업으로 필요한 스프레이 자동 도포 장비를 개발하였으며, 스프레이 도포 시 균일하게 미세 분말이 도포 될 수 있도록 파라미터 세팅에 대해 실험적으로 연구하였다. 결과적으로 빠르고 쉬운 자동 스프레이 도포 장비가 개발 되었고, 이를 활용해서 3D 측정을 위한 준비 시간이 기존 대비 1/10수준으로 단축되었다. 또한 다양한 조건에 대한 비교를 통해 최적의 도포 조건을 실험적으로 제시하였다.

• 감성과학
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• 제14권1호
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• pp.165-174
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• 2011

최근 IT 융합 기술이 글로벌 시장의 핵심 화두로 떠오르면서, 스마트 의류 분야에서도 '의류+서비스 제공(service provider)' 기능을 갖는 PSS형 제품 디자인에 대한 수요가 크게 증가하고 있다. 본 연구에서는PSS형 제품 디자인의 일환으로서 안전보호 기능의 산악복 용도에 적합한 발광특성을 지닌 유연 광섬유 기반 직물 디스플레이의 제직구성을 모색하고, 이를 적용한 산악복 모형 디자인을 제시하였다. 이를 위하여 제직 구성, 즉 직물조직과 광섬유 밀도가 다른 총 15개 광섬유 직물 디스플레이 시료를 제직하여, 이를 대상으로 각각의 휘도를 측정함으로써 발광특성을 분석하였다. 그 결과, '주자직 2:1', '주자직 3:1' 및 '능직 2:1', '능직 3:1'인 경우가 안전보호 기능을 위한 산악복으로서 적용이 가장 적합한 발광효과를 보이는 것으로 나타났다. 발광특성에 관한 분석 결과 및 최근 스포츠 패션 트렌드를 기초로 하여, 유연 광섬유 직물 디스플레이 적용 산악복 모형 디자인을 전개하였다.

• Corrosion Science and Technology
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• 제9권4호
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• pp.147-152
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• 2010

Conventional paints for conversion coating applications in steel production derived mainly from water-based polymer dispersions containing several additives actually show good general performance, but suffer from poor scratch and abrasion resistance during use. The reason for this is because the relatively soft organic binder matrix dominates the mechanical surface properties. In order to maintain the high quality and decorative function of coated steel sheets, the mechanical performance of the surface needs to be improved significantly. In fact the wear resistance should be enhanced without affecting the optical appearance of the coatings by using appropriate nanoparticulate additives. In this direction, nanocomposite coating compositions (Nanomer$^{(R)}$) have been derived from water-based polymer dispersions with an increasing amount of surface-modified nanoparticles in aqueous dispersion in order to monitor the effect of degree of filling with rigid nanoparticles. The surface of nanoparticles has been modified for optimum compatibility with the polymer matrix in order to achieve homogeneous nanoparticle dispersion over the matrix. This approach has been extended in such a way that a more expanded hybrid network has been condensed on the nanoparticle surface by a hydrolytic condensation reaction in addition to the quasi-monolayer type small molecular surface modification. It was expected that this additional modification will lead to more intensive cross-linking in coating systems resulting in further improved scratch-resistance compared to simple addition of nanoparticles with quasi-monolayer surface modification. The resulting compositions have been coated on zinc-galvanized steel and cured. The wear resistance and the corrosion protection of the modified coating systems have been tested in dependence on the compositional change, the type of surface modification as well as the mixing conditions with different shear forces. It has been found out that for loading levels up to 50 wt.-% nanoparticles, the mechanical wear resistance remains almost unaffected compared to the unmodified resin. In addition, the corrosion resistance remained unaffected even after $180^{\circ}$ bending test showing that the flexibility of coating was not decreased by nanoparticle addition. Electron microscopy showed that the inorganic nanoparticles do not penetrate into the organic resin droplets during the mixing process but rather formed agglomerates outside the polymer droplet phase resulting in quite moderate cross linking while curing, because of viscosity. The proposed mechanisms of composite formation and cross linking could explain the poor effect regarding improvement of mechanical wear resistance and help to set up new synthesis strategies for improved nanocomposite morphologies, which should provide increased wear resistance.

• Bulletin of the Korean Chemical Society
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• 제35권2호
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• pp.505-512
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• 2014

A new donor-accepter-donor-accepter-donor (D-A-D-A-D) type 2,1,3-benzothiadiazole-thiophene-based acceptor unit 2,5-di(4-(5-bromo-4-octylthiophen-2-yl)-2,1,3-benzothiadiazol-7-yl)thiophene ($DTBTTBr_2$) was synthesized. Copolymerized with fluorene and indeno[1,2-b]fluorene electron-rich moieties, two alternating narrow band gap (NBG) copolymers PF-DTBTT and PIF-DTBTT were prepared. And two copolymers exhibit broad and strong absorption in the range of 300-700 nm with optical band gap of about 1.75 eV. The highest occupied molecular orbital (HOMO) energy levels vary between -5.43 and -5.52 eV and the lowest unoccupied molecular orbital (LUMO) energy levels range from -3.64 to -3.77 eV. Potential applications of the copolymers as electron donor material and $PC_{71}BM$ ([6,6]-phenyl-$C_{71}$ butyric acid methyl ester) as electron acceptors were investigated for photovoltaic solar cells (PSCs). Photovoltaic performances based on the blend of PF-DTBTT/$PC_{71}BM$ (w:w; 1:2) and PIF-DTBTT/$PC_{71}BM$ (w:w; 1:2) with devices configuration as ITO/PEDOT: PSS/blend/Ca/Al, show an incident photon-to-current conversion efficiency (IPCE) of 2.34% and 2.56% with the open circuit voltage ($V_{oc}$) of 0.87 V and 0.90 V, short circuit current density ($J_{sc}$) of $6.02mA/cm^2$ and $6.12mA/cm^2$ under an AM1.5 simulator ($100mA/cm^2$). The photocurrent responses exhibit the onset wavelength extending up to 720 nm. These results indicate that the resulted narrow band gap copolymers are viable electron donor materials for polymer solar cells.

• 한국재료학회지
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• 제30권8호
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• pp.406-412
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• 2020

SrMoO₄:RE³⁺ (RE=Dy, Sm, Tb, Eu, Dy/Sm) phosphors are prepared by co-precipitation method. The effects of the type and the molar ratio of activator ions on the structural, morphological, and optical properties of the phosphor particles are investigated. X-ray diffraction data reveal that all the phosphors have a tetragonal system with a main (112) diffraction peak. The emission spectra of the SrMoO₄ phosphors doped with several activator ions indicate different multicolor emissions: strong yellow-emitting light at 573 nm for Dy³⁺, red light at 643 nm for Sm³⁺, green light at 545 nm for Tb³⁺, and reddish orange light at 614 nm for Eu³⁺ activator ions. The Dy³⁺ singly-doped SrMoO₄ phosphor shows two dominant emission peaks at 479 and 573 nm corresponding to the ⁴F_9/2→⁶H_15/2 magnetic dipole transition and ⁴F_9/2→⁶H_13/2 electric dipole transition, respectively. For Dy³⁺ and Sm³⁺ doubly-doped SrMoO₄ phosphors, two kinds of emission peaks are observed. The two emission peaks at 479 and 573 nm are attributed to ⁴F_9/2→⁶H_15/2 and ⁴F_9/2→⁶H_13/2 transitions of Dy³⁺ and two emission bands centered at 599 and 643 nm are ascribed to ⁴G_5/2→⁶H_7/2 and ⁴G_5/2→⁶H_9/2 transitions of Sm³⁺. As the concentration of Sm³⁺ increases from 1 to 5 mol%, the intensities of the emission bands of Dy³⁺ gradually decrease; those of Sm³⁺ slowly increase and reach maxima at 5 mol% of Sm³⁺ ions, and then rapidly decrease with increasing molar ratio of Sm³⁺ ions due to the concentration quenching effect. Fluorescent security inks based on as-prepared phosphors are synthesized and designed to demonstrate an anti-counterfeiting application.

• 한국결정성장학회지
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• 제23권2호
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• pp.93-100
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• 2013

지구 온난화의 대표적인 주범인 $CO_2$를 저감하기 위하여 많은 연구가 진행되고 있다. 특히 가스 하이드레이트 형성원리를 이용한 $CO_2$ 분리 및 저장 공정이 주목을 받고 있다. 본 연구는 필름형 $CO_2$ 하이드레이트의 결정성장 거동에 관하여 성장 메커니즘을 규명하였다. 다양한 압력조건에서 반회분식 교반 반응기를 이용하여 $CO_2$ 하이드레이트를 형성시켰으며 객체가스의 용해도 차이를 최소화하기 위하여 모든 실험에서 온도는 고정하였다. 공급된 가스는 순도 99.999 %의 $CO_2$ 가스를 사용하였고, CCD 카메라(Nikon DS-5M/Fi1/2M-U2)가 장착된 광학현미경을 사용하여 관찰 결과를 실시간 기록하였다. 실험에 적용되는 압력에 따라서 하이드레이트 성장형태와 성장속도는 매우 큰 차이를 보였다. 특히 2.0 MPa 이상의 압력에서 가장 큰 변화를 관찰하였으며, 이것은 $CO_2$의 농도 차이와 모세관 힘에 의한 것으로 사료된다.

• 한국정보통신학회논문지
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• 제8권6호
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• pp.1107-1114
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• 2004

시스템 패킷 인터페이스 4레벨 2단계(System Packet Interface Leve14 Phase 2)는 10Gbps 이더넷응용 뿐만 아니라, OC-192 대역폭의 ATM 및 POS를 통한 패킷 또는 셀 전송을 위한 물리계층과 링크계층 소자간의 인터페이스이다. SPI-4.2 코어는 전송 인터페이스 블록과 수신 인터페이스 블록으로 구성되어 있으며, 전이중 통신을 지원한다. 전송부는 사용자 인터페이스로부터 64비트의 데이터와 14비트의 헤더 정보를 비동기 FIFO에 쓰고, PL4 인터페이스를 통해 DDR 데이터를 전송한다. 그리고 수신부의 동작은 전송부와 역으로 동작한다. 전송부와 수신부는 캘런더 메모리를 컨피규레이션함으로서 최대 256개의 채널 지원이 가능하고, 대역폭 할당을 제어할 수 있도록 설계하였다 DIP-4 및 DIP-2 패리티 생성 및 체크를 자동적으로 수행하도록 구현하였다. 설계된 코어는 자일링스 ISE 5.li 툴을 이용하여 VHDL언어를 사용하여 기술하였으며, Model_SIM 5.6a를 이용하여 시뮬레이션 하였다. 설계된 코어는 라인당 720Mbps의 데이터 율로 동작하였다. 따라서 총 11.52Gbps의 대역폭을 지원할 수 있다. SPI-4.2 인터페이스 코어는 기가비트/테라비트 라우터, 광학 크로스바 스위치 및 SONET/SDH 기반의 전송 시스템에서 라인카드로 사용할 경우 적합할 것으로 사료된다.

• 전기의세계
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• 제28권4호
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• pp.53-63
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• 1979

Interface recombination velocity in $Al_{x}$G $a_{1-x}$ As-GaAs and $Al_{0.85}$, G $a_{0.15}$ As-GaA $s_{1-y}$S $b_{y}$ heterojunction systems is studied as a function of lattice mismatch. The results are applied to the design of highly efficient III-V heterojunction solar cells. A horizontal liquid-phase epitaxial growth system was used to prepare p-p-p and p-p-n $Al_{x}$G $a_{1-x}$ As-GaA $s_{1-y}$S $b_{y}$-A $l_{x}$G $a_{1-x}$ As double heterojunction test samples with specified values of x and y. Samples were grown at each composition, with different GaAs and GaAs Sb layer thicknesses. A method was developed to obtain the lattice mismatch and lattice constants in mixed single crystals grown on (100) and (111)B oriented GaAs substrates. In the AlGaAs system, elastic lattice deformation with effective Poisson ratios .mu.$_{eff}$ (100=0.312 and .mu.$_{eff}$ (111B) =0.190 was observed. The lattice constant $a_{0}$ (A $l_{x}$G $a_{1-x}$ As)=5.6532+0.0084x.angs. was obtained at 300K which is in good Agreement with Vegard's law. In the GaAsSb system, although elastic lattice deformation was observed in (111) B-oriented crystals, misfit dislocations reduced the Poisson ratio to zero in (100)-oriented samples. When $a_{0}$ (GaSb)=6.0959 .angs. was assumed at 300K, both (100) and (111)B oriented GaAsSb layers deviated only slightly from Vegard's law. Both (100) and (111)B zero-mismatch $Al_{0.85}$ G $a_{0.15}$As-GaA $s_{1-y}$S $b_{y}$ layers were grown from melts with a weight ratio of $W_{sb}$ / $W_{Ga}$ =0.13 and a growth temperature of 840 to 820 .deg.C. The corresponding Sb compositions were y=0.015 and 0.024 on (100) and (111)B orientations, respectively. This occurs because of a fortuitous in the Sb distribution coefficient with orientation. Interface recombination velocity was estimated from the dependence of the effective minority carrier lifetime on double-heterojunction spacing, using either optical phase-shift or electroluminescence timedecay techniques. The recombination velocity at a (100) interface was reduced from (2 to 3)*10$^{4}$ for y=0 to (6 to 7)*10$^{3}$ cm/sec for lattice-matched $Al_{0.85}$G $a_{0.15}$As-GaA $s_{0.985}$S $b_{0.015}$ Although this reduction is slightly less than that expected from the exponential relationship between interface recombination velocity and lattice mismatch as found in the AlGaAs-GaAs system, solar cells constructed from such a combination of materials should have an excellent spectral response to photons with energies over the full range from 1.4 to 2.6 eV. Similar measurements on a (111) B oriented lattice-matched heterojunction produced some-what larger interface recombination velocities.ities.ities.s.

• 폴리머
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• 제38권6호
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• pp.752-759
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• 2014

본 연구에서는 미세 전자 소자용 절연박막 및 차세대 플렉시블 디스플레이 기판으로서 사용이 기대되는 폴리이미드(PI)에 개환 복분해 중합(ring-opening metathesis polymerization)이 가능한 환형 말단 캡핑제(end-capping agent)인 cis-1,2,3,6-tetrahydrophthalic anhydride(CDBA)로 사슬 말단에 가교 반응이 된 가교형 폴리이미드를 합성하였다. 말단 캡핑제의 조성비에 따른 가교형 폴리이미드 박막의 잔류응력 거동은 thin film stress analyzer(TFSA)를 이용한 wafer bending mothod로 온도에 따라 연속적인 거동을 in-situ로 측정하였다. 열특성은 시차 주사 열량계(DSC), 열기계 분석기(TMA) 및 열 중량 분석기(TGA)를 이용하여 측정하였고, 광학 특성은 자외선/가시광선 분광광도계(UV-vis)와 색차계(spectrophotometer)를 이용하였으며, 네트워크 구조의 모폴로지(morphology) 변화를 통해 해석하였다. 말단 캡핑제의 조성비가 증가함에 따라 잔류응력은 27.9에서 -1.3 MPa로 초저응력 및 향상된 열 특성을 나타내었으나, 광학 특성은 감소됨을 보였다. 가교형 폴리이미드 박막의 우수한 특성 발현은 고집적도 다층 구조의 안정성 및 신뢰도가 요구되는 분야의 응용성이 확대될 것으로 기대된다.

• 한국환경보건학회지
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• 제44권1호
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• pp.55-62
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• 2018

Objectives: This study set out to measure the heavy metal concentrations in waste water produced in the casting pickling process at dental technical laboratories and examine the actual state of its treatment. Methods:The investigator measured the concentrations of each heavy metal at 55 dental technical laboratories using an inductively coupled plasma optical emission system. Results: The annual usage of electrolytes was under 10 L in 50 (90.9%), and was 10L or more in five (9.1%) laboratories. Among the laboratories, 15 (27.3%) commissioned the treatment of waste,12 (21.8%) treated the waste with general sewage,and 28 (50.9%) treated the waste in aseptic tank. The arithmetic $mean{\pm}standard$ deviation and the geometric mean of chrome(Cr) were $75.3{\pm}50.9$ and 58.3 mg/L; those of cobalt (Co) were $112.3{\pm}106.7$ and 66.1 mg/L; those of nickel (Ni) were $62.9{\pm}83.5$ and 8.9 mg/L; those of molybdenum (Mo) were $17.1{\pm}13.4$ and 12.0 mg/L; those of iron (Fe) were $31.5{\pm}44.1$ and 6.2 mg/L; those of lead (Pb) were $0.3{\pm}0.3$ and 0.3 mg/L; those of beryllium (Be) were $3.6{\pm}3.6$ and 2.0 mg/L. The hydrogen ion concentration was under pH 2 across all the samples. Conclusions: The findings show that the dental technical laboratories were not doing well with the separation, storage, collection, and treatment of the electrolytes they discarded, and that most of the electrolytes were introduced through the general sewage or aseptic tank. The causes of this include alack of perception among the practitioners at dental technical laboratories and contracted companies avoiding collection for economic reasons. There is a need for education to improve the perceptions of waste water treatment among the practitioners at dental technical laboratories. Environment-related departments should be stricter with legal applications in the central and local governments. It is also required to provide proper management of commissioned treatment.