• 폴리머
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• 제34권1호
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• pp.38-44
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• 2010

탄산칼슘/유기계 core-shell 입자를 제조하기 위해 core로는 침강성 탄산칼습을 사용하였고, shell로서는 여러 종류의 methyl methacrylate(MMA), ethyl acrylate(EA), n-butyl acrylate(BA), styrene(St), 2-ethylhexyl acylate(2-EHA)을 사용하여, 반응 온도 유화제, 개시제의 종류와 첨가량을 변화시킨 후에 유화중합을 시켜 최적의 유화중합 조건을 구하였다. 생성된 core-shell 입자의 구조는 FT-IR로, 입자크기와 형태는 입도 분석, SEM, TEM으로 각각 측정하였다. 그리고, 이 core-shell 입자에 부직포를 함침시켜 처리전후의 표면변화는 접촉각으로 확인하였다. 또한, 함침 처리 전후의 부직포/부직포 소재와 관능성 단량체 첨가한 부직포/부직포 소재의 박리 접착강도를 측정하여 상호 비교하였다. 탄산칼슘/유기 core-shell 입자 합성의 경우에는 유화제인 SDBS를 0.5 wt% 첨가한 탄산칼슘을 core로 하여 MMA와 0.1 wt% 농도의 APS를 단계적으로 주입하여 중합함으로써 탄산칼슘입자 표면에 단량체의 중합이 잘 유도될 수 있었으며 중합 도중에 새로운 중합체 입자의 생성이 적었다.

• 상하수도학회지
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• 제31권6호
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• pp.491-499
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• 2017

The chemical structures of perfluorinated compounds(PFCs) have unique properties such as thermal and chemical stability that make them useful components in a wide variety of consumer and industrial products. Two of these PFCs, perfluorooctane sulfonate(PFOS) and perfluorooctanoic acid(PFOA), have received attention and were the most commonly detected. In this study it was analyzed the concentrations of 8 PFCs in samples were collected from drinking water treatment plants for 5 years(2012-2016). PFOS and PFOA were also high concentration and frequency. The mean concentrations of PFOA and PFOS were detected $0.0026-0.0069{\mu}g/L$ and $0.0009-0.0024{\mu}g/L$ in samples from drinking water treatment plants. These were relatively lower or similar compared to PFOS concentrations in Osaka(Japan). In general, these levels are below health-based values set by international authoritative bodies for drinking water. These results will be serve as the first monitoring data for PFCs in drinking water and be useful for characterizing the concentration distribution and management of PFCs in future studies.

• 공업화학
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• 제7권1호
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• pp.101-108
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• 1996

본 연구에서는 수용액 내에서 생분해도가 우수하고 인체에 mild한 비이온성 계면활성제 GL12와 범용 음이온성 계면활성제인 linear laurylbenzene sulfonate(LAS) 또는 sodium polyoxyethylene(3) glycol lauryl ether sulfate(SLES) 각각 용액의 dynamic surface tension과 이들 계면활성제 혼합용액의 dynamic surface tension이 혼합비에 따라 어떻게 변화되는지 maximum bubble pressure method를 이용하여 조사하였다. 또한 salting-cut 효과가 있는 NaCl, CsCl과 salting-in 효과가 있는 요소를 계면활성제 용액에 첨가하여 이들 염들이 용액의 dynamic surface tension에 미치는 영향에 대하여도 연구하였다. 비이온성 계면활성제인 GL12의 dynamic surface tension은 염의 존재에 영향을 크게 받지 않았으나 음이온성인 SLES와 LAS는 크게 영향을 받았다. 또한 GL12/SLES와 GL12/LAS 혼합계에서도 GL12의 함량이 많을수륵 용액의 dynamic surface tension에 대한 염의 영향이 감소하였으나 LAS 또는 SLES의 함량이 증가할수록 염의 영향은 증가하였다.

• 한국환경과학회지
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• 제6권1호
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• pp.45-52
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• 1997

Methyl methanesulfonate (MMS) was fed to Drosophila melnogaster in order to investigate its toxic capability at developmental and adult stages, and the hereditary effect of toxicity and the potency for induction of sex-linked lethal mutation during the slyer-matogenesis by the means of an attached-X method. In the control group, the egg to adult viability of D. melnogaster was 95.2%, while 3. 5mM and 5.0mM treated groups were 90.0% and 84.1%, respectively. In the case of their progenies (Fl), the viability was 96.9% in the control group, while 3.5mM and 5.0mM treated groups were 54.5% and 1.6%, respectively. Therefore, these differences between two generations show significant physiological toxic effects in the next generation. In the parental generation, the developmental time was calculated 11.05 days in the control group, 12.43 days In 3.5%mM treated group, and 13.23 days in 5.0mM. In the case of Fl it was estimated 10.35 days in the control group, and 11.43 days In 3.5mM treated group. Compared with the control groups In two generations, the developmental time generally delayed as the dose of MMS increased. As to the sex-ratio, there was no differences between the control and MMS treated groups. The toxic values of adult stage showed which increased the frequency of mortality with MMS concentrations. The mortality at 120hr In the control group was 1.67% and it in 0.5mM MMS treated group 3.33%. In 2.5mM MMS treated group, it was 33.3% at 72hr, and it 95% at 120hr The increase of the morality was shown from 72hr in 4.0mM treated group which was 100% at 96hr. There was the concentration-dependent induction of sex-linked lethal mutation during the spermatogenesis by means of an attached-X method, MMS had more pronounced effect in sperm and spermaid stages in D. melnogaster.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2008년도 추계학술대회 논문집 Vol.21
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• pp.396-396
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• 2008

투명 전도성 탄소나노튜브(carbon nanotube, CNT) 필름을 터치스크린이나 디스플레이 소자 등의 전극에 응용할 목적으로, CNT 필름의 전기저항 및 광 투과도를 향상시키기 위한 연구가 활발히 진행되고 있다. 본 연구에서는 단일벽 CNT (single-walled CNT)를 여러 가지 계면활성제로 분산시킨 수용액으로부터 제조한 CNT 필름을 산 처리하여 저항 및 투과도의 변화를 관찰하였다. 우선 계면활성제로 분산시킨 CNT 수용액을 알루미나 재질의 필터에서 정량적으로 진공 필터링하여 CNT 필름을 제조하였다. 알루미나 필터를 sodium hydroxide (NaOH) 수용액으로 용해시켜 제거함으로써 얻은 CNT 필름을 유리기판 위에 부착시킨 후 광 투과도와 먼 저항 (sheet resistance)을 측정하였다. CNT 필름을 질산 ($HNO_3$) 용액에 처리하였을 때 투과도는 1~5 % 향상되었으며, 면 저항은 계면활성제로 분산시킨 CNT 필름 대부분에서 감소하였다. 이는 CNT 표면에 코팅되어 있던 계면활성제들이 산에 의해 제거되었기 때문일 것으로 추측된다. 특히 sodium dodecylbenzene sulfonate (NaDDBS)로 제조한 CNT 필름의 경우, 질산을 처리 전에는 투과도 83%, 면 저항 450 $\Omega$/sq.의 특성을 보였으나, 처리 후에는 각각 86 %, 350 $\Omega$/sq.로 향상되었다. Polyvinyl pyrrolidone (PVP)과 cetyltrimethylammonium bromide (CTAB)를 사용하여 제조한 CNT 필름의 면 저항이 가장 뚜렷한 감소를 보였다. 제조된 필름과 삼 처리된 필름 특성을 Raman spectroscopy, scanning electron microscopy, UV-Vis spectroscopy 등을 이용하여 분석하였고, 4-point probe로 면 저항을 측정하였다.

• 한국환경과학회지
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• 제22권8호
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• pp.1009-1017
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• 2013

Perfluorooctanoic acid (PFOA) and perfluorooctyl sulfonate (PFOS) is a new persistent organic pollutants of substantial environmental concern. This study investigated the potential of magnetic ion exchange resin (MIEX$^{(R)}$) as the adsorbent for the removal of PFOA and PFOS from Nakdong River water. In our batch experiments, we studied the effect of some parameters (pH, temperature, sulfate concentration) on the removal of PFOA and PFOS. The results of sorption kinetics on MIEX$^{(R)}$ show that it takes 90 min to reach equilibrium but the economical contact time and dosage were 30 min and 10 mL/L. An increase in pH (pH 6~10) leads to a decrease in PFOA (2.0%) and PFOS (3.6%) sorption on MIEX$^{(R)}$. The sorption of both PFOA and PFOS decreases with an increase in ionic strength for sulfate ion (${SO_4}^{2-}$), due to the competition phenomenon. An increase in water temperature ($8^{\circ}C{\sim}28^{\circ}C$) in water leads to a increase in PFOA (2.8%) and PFOS (4.3%) sorption on MIEX$^{(R)}$. Based on the sorption behaviors and characteristics of the adsorbents and adsorbates, ion exchange and hydrophobic interaction were deduced to be involved in the sorption, and hemi-micelles possibly formed in the intraparticle pores.

• 전기화학회지
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• 제11권4호
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• pp.304-308
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• 2008

Noble Poly (lithium 2-acrylamido-2-methyl propane sulfonate) and its copolymer with N-vinyl formamide based on trihexyl (tetradecyl) phosphonium acetate [$(C_6H_{13})_3$ P ($C_{14}H_{29}$) $CH_3COO$; $P_{66614}$ $CH_3COO$] and trihexyl (tetradecyl)phosphonium bis(trifluoromethane sulfonyl) amide ([$(C_6H_{13})_3P(C_{14}H_{29})$] [TFSA];$P_{66614}TFSA$) were prepared and analyzed to determine their characteristics and properties. The ionic conductivity of a copolymer based $P_{66614}TFSA$ ionic liquid system exhibits a higher conductivity ($8.9{\times}10^{-5}Scm^{-1}$) than that of a copolymer based $P_{66614}CH_3COO$ system ($1.57{\times}10^{-5}Scm^{-1})$. The charge on the TFSA anion is spread very diffusely through the S-N-S core and particularly in the trifluoromethane groups, and this diffusion results in a decreased interaction between the cation and the anion. The viscosity of $P_{66614}TFSA$ (39 cP at 343 K) and $P_{66614}CH_3COO$ (124 cP at 343 K), which is very hydrophobic, was fairly high. High viscosity leads to a slow rate of diffusion of redox species. The ionic conductivity of copolymer of a phosphonium ionic liquid system also exhibits higher conductivity than that of a homopolymer system. Phosphonium ionic liquids were thermally stable at temperatures up to $400^{\circ}C$.

• 한국식품영양학회지
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• 제32권6호
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• pp.611-619
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• 2019

The purpose of this study was to investigate the antioxidant activity and tyrosinase inhibitory activity of Codonopsis lanceolata 50% ethanol extract, and its solvent fractions (n-hexane, ethyl acetate (EA), n-butanol, water). The main components of the EA fraction were qualitatively analyzed using UPLC Q-ToF/MS. Additionally, a quantitative analysis was performed using UPLC. As a result, the total polyphenol content was 113.36 mg gallic acid/g in the EA fraction, which contained the largest amount of the C. lancolata solvent fractions. Also EA showed the highest antioxidant activity than other fractions. The IC₅₀ of DPPH(2,2-diphenyl-1-picrylhydrazyl) radical scavenging activity was 0.03 mg/mL and the IC₅₀ of ABTS [2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate)] radical scavenging activity was 0.049 mg/mL. The EA fraction showed tyrosinase inhibitory activity than other fractions and especially inhibited monophenolase oxidase reaction higher than diphenolase oxidase reaction. The monophenolase oxidase inhibited 55% when the concentration of the EA fraction was 0.25 mg/mL. As a result of Q-ToF/MS analysis, it was confirmed that tangshenoside I and lobetyolin were the main components of EA fraction. Thus, these results suggest that C. lanceolata may be used as a potent source of cosmetic agents.

• 한국결정성장학회지
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• 제14권1호
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• pp.12-16
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• 2004

본 실험은 대형의 고품질 DAST 결정을 위한 결정안정성과 재현성의 향상에 관하여 연구하였다. DAST 결정은 냉각법에 의한 메탄을 포화용액에서 성장시켰으며, 4-methyl-n-methyl pyridinum tosylate의 축합상태로 합성하였다. DAST 분말은 piperidine이 존재한 상태에서 r-picoline. methyl p-tolune sulfonate 그리고 P-dimethylaminobenzaldehyde로부터 제조하였다. 이때 DAST $H_2O$의 생성을 피하기 위하여 dry Argon분위기에서 합성하였다. 이것은 DAST분자가 습한 분위기에서 결정화될 경우 결정구조는 중심 대칭이 되고 그러한 경우에 DAST 미세결정이 습기를 함유하면 2차 비선형 광학특성은 사라지기 때문이다. 우리는 성장방향을 (001)면으로 고정시켰다. 성장조건은 $H_2O$/day로 서냉시켰으며 기간은 4일 동안이었다. seed 결정의 크기는 $2.5\times 3.6\times0.4\textrm{mm}^3$이며 $10\times 10.5\times3.0\textrm{mm}^3$의 DAST 결정을 제조했다. 육성된 DAST는 빨간색이며 메탈릭그린처림 보이는 표면특성을 나타내였다.

• Journal of Electrochemical Science and Technology
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• 제11권1호
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• pp.50-59
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• 2020

Birnessite-type manganese dioxide (δ-MnO₂) with hierarchical micro-/mesoporosity was synthesized via sacrificial graphene template approach under mild hydrothermal conditions for the first time. Graphene template was obtained by a surfactant (cetyltrimethylammonium bromide, CTAB) assisted liquid phase exfoliation (LPE) in water. A thin PEDOT:PSS (poly (3,4-ethylene dioxythiophene): poly (styrene sulfonate)) layer was applied to improve electrical conductivity and rate capability of MnO₂. The MnO₂ (535 F g^-1 at 1 A g^-1 and 45 F g^-1 at 10 A g^-1) and MnO₂/PEDOT:PSS nanocomposite (550 F g^-1 at 1 A g^-1 and 141 F g^-1 at 10 A g^-1) delivered electrochemical performances superior to their previously reported counterparts. An asymmetric supercapacitor, composed of MnO₂/PEDOT:PSS (positive) and Fe₃O₄/Carbon (negative) electrodes, provided a maximum specific energy of 18 Wh kg^-1 and a maximum specific power of 4.5 kW kg^-1 (ΔV= 2 V, 1M Na₂SO₄) with 85% capacitance retention after 1000 cycles. The graphene-templated MnO₂/PEDOT:PSS nanocomposite obtained by a simple and green approach promises for future energy storage applications with its remarkable capacitance, rate performance and cycling stability