• The Korean Journal of Rheology
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• v.9 no.1
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• pp.6-15
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• 1997

계면활성제용액에 서로 다른 기능을 하는 두 종류의 첨가제를 투입하여 미셀의 미 세구조 전이현상을 규명하였다. 양이온 계면활성제는 CMC 이상의 농도에서 2단계의 미세 구조 전이거동을 나타낸다. 우선 구형 미셀은 첨가제의 투입에 의하여 표면에서의 친수성기 간의 반발력이 감소됨으로써 실린더형 또는 디스크형미셀로 전이가 일어난다. 더욱 농도가 증가하면 이방성을 가지는 실린더형 미셀간의 중첩 또는 hooking 현상에 의한 두 번째 전 이가 일어난다. 이때 미셀 용액은 흔히 점탄성을 나타내거나 확연한 비뉴톤성 유체거동을 나타낸다. 본 연구에선 heptanol의 화확구조적 차이가 물성에 나타내는효과를 규명하고 wormlike 미셀을 형성하는 MaSal에 의한 점탄성 거동을 살펴보았다. Heptanol의 화학구조 의 영향을 보면 약친수성기인 OH기가 알킬그룹과 나란하게 존재하여 밀집된 구조를 가지 기 쉬운 primary heptanol이 가장효과적으로 미세구조 전이를 유도함을 관찰하였다. 다른 이성질 hetanol의 경우 secondary heptanol이 teriary heptanol에 비하여 효과적임을 보이지 만 화학재할수 있는 농도범위가 매우 좁아 대부분 영역에서 비뉴톤성거동을 나타냄을 확인 하였다. 즉 NaSal를 사용한 경우 실린더형 미셀이 존재할 수 있는농도범위가 매우 좁아 대 부분 영역에서 비뉴톤성 거동을 나타냄을 확인하였다. 즉 NaSal 이 첨가된 용액은 선형점탄 성거동을 보이며 몰비가 증가함에 따라 scission 과정이 관찰되었다. 또한 몰농도비에 따라 항복응력과 shear thickening 특징을 보이는데 이는 흐름장의 세기에 따라 미세구조 변화가 일어나기 때문이다.

• Polymer(Korea)
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• v.27 no.1
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• pp.17-25
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• 2003

Using atom transfer radical polymerization (ATRP), polystyrene macroinitiators and polystyrene-b-poly(t-butyl acrylate) (PS-b-P(tBA) block copolymers were synthesized by CuBr/PMDETA catalyst system in solution. After hydrolysis, polystyrene-b-poly(acrylic acid), amphiphilic block copolymers, were formed. Subsequent neutralization of polyacid block led to the block ionomers. The molecular weight of the synthesized PS-b-P(tBA) block copolymers was easily-controlled to 5000-10000 and their distributions were less than 1.2. The chemical structures of the synthesized block copolymers were characterized by $^1$H-NMR and FT-IR. In the DSC thermograms, $T_g$ appeared in the vicinity of 100 $^{\circ}C$ because of higher styrene content. In addition, the phase separation of the block ionomers was observed by TEM.

• Proceedings of the Korean Vacuum Society Conference
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• 2013.08a
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• pp.182.2-182.2
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• 2013

최근 산화아연이나 산화주석을 기반으로 한 산화물 박막 트랜지스터의 연구가 활발히 진행중이다. 2004년 Hosono 그룹에서 비정질 InGaZnO (IGZO) 박막을 이용한 TFT소자 제작을 보고하고 우수한 특성을 확인 후 산화물 TFT 소자기술에 대한 전 세계적인 연구개발의 발판이 마련되었다. 그러나 다성분계 화합물로 이루어진 산화물 반도체의 경우 복잡한 성분 조합과 조절이 어렵고, 장비의 제약으로 상용화에 어려움을 겪고 있다. 산화아연의 경우 증착시 쉽게 결정화가 이루어져 대면적 균일성을 확보하기 어렵고, 결정립계에 의한 이동도 저하, DC 신뢰성 저하의 문제가 발생한다. 이에 비해 산화주석의 경우 증착공정에 따라 비정질상과 결정립상을 조절할 수 있다. 하지만, 현재까지 발표된 산화주석 기반의 박막 트랜지스터는 내부 캐리어의 조절이 상대적으로 어려운 단점이 보고되었다. 본 연구에서는 산화 주석기반의 박막 트랜지스터를 제작하고 이에 Zr이온을 도핑하여 소자 특성을 개선시키고 동작모드를 조절하는 연구를 진행하였다. Bottom gate 형식의 ZrSnO TFT를 제작하였고 전이 특성을 살펴본 결과 Zr의 함량이 늘어날수록 이동도는 감소하는 경향이 나타났다. 또한 Zr의 미량 함량에도 불구하고 산소결핍에 의한 캐리어 생성을 억제하여, 소자 특성을 공정조건에 따라 조절할 수 있는 가능성을 확인 했다.

• Proceedings of the Korean Vacuum Society Conference
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• 2010.08a
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• pp.103-103
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• 2010

최근 산화물 반도체 기반의 박막 트랜지스터에 대한 연구가 활발히 진행되고 있으며 이는 공간 점유와 시각적 제약을 해소하려는 시장의 요구에 의해 주도되고 있다. 특히, 2004년 Hosono 그룹에서 비정질 InGaZnO (IGZO) 박막을 이용한 TFT소자 제작을 발표하고 우수한 특성을 확인한 후 산화물 TFT 소자기술에 대한 전 세계적인 연구개발의 계기가 마련되었다. 그러나 다성분계 화합물로 이루어진 산화물 반도체의 경우 복잡한 성분 조합과 조절이 어렵고, 장비의 제약으로 인해 상업화에 어려움을 겪고 있다. 따라서 이성분계 물질인 산화아연의 경우 아직까지 상업화 이점이 남아있으며, 우수한 전기적 성질과 광학적 장점이 있기에 그 가능성은 더욱 커지고 있다. 그럼에도 불구하고 산화아연계 박막 트랜지스터의 경우 바이어스에 의해 동작전압이 이동하는 DC신뢰성의 문제점이 남아 있고, 이를 해결하기 위해 안정적인 절연막 또는 보호막을 도입하려는 연구가 많이 시도되고 있다. 본 연구에서는 산화아연기반의 박막 트랜지스터에 Hf이온을 도핑하여 DC 신뢰성을 향상시키는 연구를 진행하였다. Bottom gate 형식의 HfZnO TFT를 제작하였고 전이 특성을 살펴본 결과 Hf의 함량이 늘어날수록 이동도는 감소하는 경향이 나타났다. 또한 Hf의 미량 도핑에도 불구하고 산소결핍에 의한 결함 생성을 억제하여 DC신뢰성이 상당히 향상되었으며, 이는 특히 산화물 반도체와 절연막 사이의 결함을 억제하여 생긴 결과로 생각된다.

• Journal of the Korean Magnetics Society
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• v.16 no.1
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• pp.6-10
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• 2006

The sulphur spinel $FeCr_{2-x}M_xS_4$(M=Ga, In) have been studied with Mossbauer spectroscopy, x-ray diffraction (XRD), and vibrating sample magnetometer. The XRB patterns for samples $FeCr_{2-x}M_xS_4$(M=Ga, In: x=0.1, 0.3) reveal a single phase, which the Ga and In ions are partially occupied to the tetrahedral (A) site. The Neel temperature for the Ga substituted samples increases from 180 to 188 K, with increase from x=0.1 to 0.3. While, it decreases from 173 to 160 K, for the In substituted samples of the x=0.1 and 0.3, respectively. The Mossbauer spectra were collected from 4.2 K to room temperature. We have analyzed the Mossbauer spectra using eight Lorentzian lines fitting method for the $FeCr_{2-x}In_xS_4$(x=0.1) at 4.2 K, yielding the 1311owing results; $H_{hf}=146.0kOe,\;{\Delta}E_Q=1.88mm/s,\;\theta=36^{\circ},\;\phi=0^{\circ},\;\eta=0.6$, and R=1.9. The Ga ions enter into the both sites octahedral (B) and tetrahedral (A), simultaneously the same amounts of Fe ions migrate from the A to the B site, this result is an agreement with XRD results, too. The ${\Delta}E_Q$ of the A and B site in Mossbauer spectra of the samples $FeCr_{2-x}Ga_xS_4$(x=0.3) are 0.83 and 2.94mm/s, respectively. While they are 0.56 and 2.36mm/s for the $FeCr_{2-x}In_xS_4$(x=0.3). It is noticeable that the ${\Delta}E_Q$ for the Ga doped samples are larger than that of the corresponding In doped samples, in spite of the larger ionic radius for In ions. The bond lengths of Cr-S, for the Ga and In doped samples (x=0.3) are found to be 2.41 and $2.43\;{\AA}$, respectively. We interpret that the larger covalence effect from the smaller bond length induces a large asymmetric charge distribution. Finally, it gives a large quadrupole interaction.

• Journal of dental hygiene science
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• v.11 no.2
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• pp.69-76
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• 2011

The aim of this study was to compare the effects on the resistance to demineralization by the frequency and method of fluoride application in vitro. ninety-one human enamel specimens were embedded in acrylic resin with the labial surfaces exposes. The specimens were divided into 7 groups; (1) non-treated; (2) 1.23% APF gel 1 time; (3) 2% NaF sol 1 time; (4) 2% NaF sol iontophoresis 1 time; (5) 1.23% APF gel 4 time; (6) 2% NaF sol 4 time; (7) 2% NaF sol iontophoresis 4 time. All the groups were immersed in the remineralizing solution (RS) before baseline and divided into 7 test groups of 13 specimens each. All the specimens were exposed to a pH-cycling model which consisted of demineralization (6 hours) and remineralization (18 hours) for 5 days. The Vickers surface micro-hardness number of all the specimens was measured using microhardness tester and the specimen surfaces were observed by scanning electron microscope (SEM). The results were analyzed using one-way ANOVA followed a Tukey's multiple comparison at a significance level of 0.05. The group 7 showed higher level of microhardness after Fluoride application. The group 1 showed lowest level of microhardness but group 7 showed higher level of microhardness after pH-cycling model, there were significant differences between groups. After the modified pH-cycling, the 2% NaF solution with the iontophoresis group showed the best resistance to demineralization(p<0.05). These results were also confirmed by SEM. The fluoride iontophoresis method was the most effective of the regimens in increasing the acid resistance of the enamel.

• Polymer(Korea)
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• v.29 no.2
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• pp.135-139
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• 2005

In this study, poly(ethylene imine) (PEI) modified by methoxypoly(ethylene glycol) (mPEG) and folate as a gene carrier was synthesized to decrease cytotoxicity and to improve in vivo targeting. mPEG was modified by glutaric anhydride (GA) to endow carboxylic end group, followed by the activation reaction with EDC (N-ethyl-N'-(3-dimethyl-aminopropyl) carbodiimide) and NHS (N-hydroxysuccinimide). The activated carboxylic end group of mPEG was reacted with the amines of PEI to give mPEG graft PEI. The mPEG-folate-graft-PEI was synthesized by the reaction of mPEG-PEI with folate pre-activated by EDC/NHS. The obtained copolymers were characterized by $^1H-NMR$ and FT-IR. Gel retardation assay and fluorescence measurement indicated that DNA formed the complexes with the synthesized copolymers above N/P charge ratio 2. The size of complexes was ranging from 100 nm to 300 m. In conclusion, we confirmed that the synthesized copolymer have the possibility as a DNA carrier.

• Analytical Science and Technology
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• v.35 no.3
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• pp.116-123
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• 2022

Polymer bags, metallic canisters, and glass bottles have been used as containers for analyzing the volatile organic compounds (VOCs) in air. In this study, various sampling containers were compared to investigate the short-term stability of VOCs, that is, from the time they are sampled to the time they are analyzed. Polyvinyl fluoride (PVF), polypropylene (PP), polyester aluminum (PE-Al) bags, canisters, and glass bottles were used as sample containers. A 100 nmol/mol standard gas mixture of benzene, toluene, ethylbenzene, m-xylene, styrene, and o-xylene was used for the VOC comparison. Changes in the concentrations of samples stored for 10~20 day in each container were measured using a thermal desorption-gas chromatograph-flame ionization detector (TD-GC-FID). As a result, VOCs stored in a canister and two kinds of amber glass bottles have shown immaterial decreases in concentration in one week, and more than 80 % of the initial concentration was maintained for two weeks. In the case of polymer bags, the concentration of all VOCs, except benzene and toluene, were remarkably decreased below 70% of the initial concentration in one day. Particularly, ethylbenzene, xylene, and styrene have shown dramatic decreases in concentration below 30 % of the initial concentration in all polymer bags in one day.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.14 no.11
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• pp.6008-6014
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• 2013

This study aimed to understand seasonal variation of physico-chemical factors and biomass of size-fractionated phytoplankton at Ulsan seaport during the period from February 2007 to November 2009. Water temperature, salinity, dissolved oxygen (DO), pH, chemical oxygen demand (COD) and total suspended solid (TSS) varied in the range of 8.94-$24.26^{\circ}C$, 25.06-34.54 psu, 4.30-10.73 mg/L, 7.97-8.53, 0.66-40.70 mg/L and 57.4-103.3 mg/L, respectively. These factors showed no clear spatial variation unlike spatial pattern of inorganic nutrients and total chlorophyll-a (chl-a) concentration as biomass. Concentration of phosphate, nitrate and silicate ranged from 0.01 to 3.03 ${\mu}M$, 0.05 to 21.62 ${\mu}M$, and 0.01 to 27.82 ${\mu}M$, respectively, with 2 times higher concentration at inner stations than that at outer stations during the study period. Within the range of total chl-a concentration (0.36-7.11 ${\mu}gL^{-1}$), higher concentration (avg. 1.88 ${\mu}gL^{-1}$) of total chl-a were observed at inner stations compared to that (avg. 0.90 ${\mu}gL^{-1}$) at outer stations. Micro-sized phytoplankton dominated total biomass of phytoplankton in spring (34.0-81.2%), summer (35.1-65.6%) and winter (3.9-62.0%). Nano- and pico-sized phytoplankton contributed 58.2-74.5% and 22.4-38.2% to total biomass of phytoplankton in autumn, respectively. However, contribution in biomass of size-fractionated phytoplankton to total phytoplankton biomass showed no clear difference between inner and outer stations. Consequently, these results indicated that spatio-temporal distribution of phytoplankton biomass at Ulsan seaport was dominated by micro-phytoplankton (avg. 52.3%) during the study period except autumn, which was closely dependent on the concentration of inorganic nutrients (p<0.05).

• Journal of the Korean Magnetics Society
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• v.20 no.5
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• pp.187-190
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• 2010

$Sn_{0.99}{^{57}Fe}_{0.01}O_2$ prepared by a sol-gel method, and studied by x-ray diffractometer, vibrating magnetometer, Superconducting quantum interference devices and M$\ddot{o}$ssbauer spectroscopy. the crystal structure were found to be a rutile tetragonal structure with space group $P4_2$/mnm, and oxygen deficiency are 5.6 % by Rietveld refinement. magnetization value were $M_s=1.95{\times}10^{-2}{\mu}_B/Fe$ at room temperature, and Curri-weiss temperature were and ${\theta}_{cw}$ = 18 k, measurement of VSM and SQUID, respectively. Mssbauer spectra of $Sn_{0.99}{^{57}Fe}_{0.01}O_2$ have been Sextet taken at various temperatures ranging from 4.2 K to RT, and isomer shift value $\delta$ = 0.18~0.36 mm/s of $^{57}Fe$ ion site all of the temperature range the state shows ferric.