• 제목/요약/키워드: Hwang Ester

검색결과 77건 처리시간 0.038초

P3HT:PCBM-based on Polymer Photovoltaic Cells with PEDOT:PSS-pentacene as a Hole Conducting Layer

  • Kim, Hyun-Soo;Hwang, Jong-Won;Park, Su-Jin;Chae, Hyun-Hee;Choe, Young-Son
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2010년도 제39회 하계학술대회 초록집
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    • pp.313-313
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    • 2010
  • The performance of polymer photovoltaic cells based on blends of poly(3-hexylyhiophene) (P3HT) and phenyl-C61-butyric acid methyl ester (PCBM) is strongly influenced by blend composition and thickness. Polymer photovoltaic cells based on bulk-heterojunction have been fabricated with a structure of ITO/poly(3, 4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS)-pentacene/poly (3-hexylthiophene) (P3HT):phenyl-C61-butyric acid methyl ester (PCBM)/Al. We have prepared PEDOT:PSS by dissolving pentacene in N-methylpyrrolidine (NMP) and mixing with PEDOT:PSS. Pentacene was added a maximum concentration of approximately 5.5mg to the PEDOT:PSS solution and sonicated for 10 min. Active layer (P3HT:PCBM) (1:1) was strongly influenced by PEDOT:PSS-pentacene. We have investigated the performance of photovoltaic device with different concentration of P3HT:PCBM (1:1) 2.0wt%, 2.2wt%, 2.4wt% and 2.6wt%, respectively. The photocurrent and power conversion efficiency (PCE) showed a maximum between 2.0wt% and 2.2wt% concentration of P3HT:PCBM. This implied that both morphology and electron transport properties of the layer influenced the performance of the present photovoltaic cells. As the concentration of P3HT:PCBM blends as an active layer was increased, the power conversion efficiency was decreased. P3HT:PCBM layer and PEDOT:PSS-pentacene layer were characterized by work function, UV-visible absorption, atomic force microscopy (AFM), X-ray diffraction (XRD) and scanning electron microscope (SEM).

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폴리머-콘크리트 복합재료 개발(I) - 폴리머-시멘트 콘크리트의 물성 - (Development of Polymer-Concrete Composite(I) - Physical Properties of Polymer-Cement Concrete Composites -)

  • 황의환;길덕수;오인석
    • 공업화학
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    • 제8권6호
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    • pp.979-984
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    • 1997
  • 폴리머 혼화제로서 styrene-butadiene rubber(SBR)라텍스, ethylene-vinyl acetate(EVA)에멀젼 및 polyacrylic ester(PAE)에멀젼을 사용하여 동일한 스럼프에서 폴리머-시멘트비를 변화시켜 공시체를 제조하여, 압축과 휨강도시험, 흡수시험, 세공분포측정 및 미세구조 관찰 등을 실시하였다. 그 결과 폴리머-시멘트비의 증가와 더불어 압축과 휨강도 모두 향상되었고, 동해에 큰 영향을 주는 모세관 공극범위의 세공량은 감소되었으며, 폴리머 시멘트비 15wt% 이상에서 연속적인 폴리머필름이 형성되었다.

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파라벤류의 방부력에 대한 화장품용 안료의 영향 (Effects of Cosmetic Pigments on the Bactericidal Activities of Parabens)

  • 조완구;이용화;황승진
    • 한국응용과학기술학회지
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    • 제27권4호
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    • pp.501-507
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    • 2010
  • In this study, we evaluate the anti-microbiological activity of paraben in eye shadows that are composed of pigments and oil binders using various analytical methods and microbiological tests. Paraben does not show the microbiological activity properly when it was used with Nylon SP$^{(R)}$ 10, Talc RF SSA$^{(R)}$, OMC Talc AS$^{(R)}$ and $BaSO_4$. In the test of fungi, Nylon SP$^{(R)}$ 10 causes the decrease of microbiological activity regardless of the type of oil binders. The pigment of Mango violet also causes the decrease of microbiological activity when ester oil binder was used. Regardless of the type of oil binder, samples containing nylon SP 10, 0.15% of methyl paraben and 0.05% of propyl paraben had not been able to maintain microbiological activity only if the concentration of parabens were increased. Trace amounts of metal ions present in pigments reduced the activity of preservatives by inactivation of hydroxyl group of paraben. It is thought that swollen nylon SP 10 in ester oil increase the absorption or interaction of parabens and swollen nylon powder causes the inactivation of paraben.

A New Phenylbutanone Glucoside from Salvia plebeia

  • Jin, Qiang-Hao;Han, Xiang-Hua;Hwang, Ji-Hye;Hong, Seong-Su;Park, Mie-On;Lee, Chul;Lee, Chang-Hee;Lee, Dong-Ho;Lee, Mi-Kyeong;Hwang, Bang-Yeon
    • Natural Product Sciences
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    • 제15권2호
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    • pp.106-109
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    • 2009
  • Phytochemical investigations of the EtOAc-soluble fraction of the whole plants of Salvia plebeia using repeated column chromatography with preparative HPLC led to the isolation of a new phenylbutanone glucoside, 4-{4-0-[6-(4-hydroxybenzoyl)-0-${\beta}$-D-glucopyranosyl]-3-hydroxyphenyl}-butan-2-one (salviaplebeiaside, 1) along with two known phenolic compounds, rosmarinic acid methyl ester (2) and luteolin-7-0-${\beta}$-D-glucoside (3). The structures of these compounds were determined on the basis of spectroscopic methods including 1D-, 2D-NMR and MS spectrometry and comparison of spectroscopic data with those of values reported in the literatures.

잣나무 송지(松脂)의 화학적(化學的) 성상(性狀)에 관(關)한 연구(硏究) (Study on chemical properties of Pinus koraiensis Sieb. et Zucc. resin)

  • 강하영;황병호
    • Journal of the Korean Wood Science and Technology
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    • 제4권1호
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    • pp.3-7
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    • 1976
  • 본(本) 실험(實驗)은 한국산(韓國産) 잣나무 생송지(生松脂)의 화학적(化學的) 성상(性狀)을 구명(究明)하여 수지화학분야(樹脂化學分野)와 송지가공(松脂加工) 이용분야(利用分野)에 기초자료(基礎資料)를 얻고자 실시(實施)하였던바, 그 화학적(化學的) 성상(性狀)이 상당(相當)한 이용가치(利用價値)가 있는 것으로 고려(考慮)되며 그 결과(結果)를 요약(要約)하면 다음과 같다. 1) 산가(酸價)는 134.12로 나타났다. 2) 영화가(齡化價)는 172.72로 나타났다. 3) 요오드가(價)는 109.93으로 나타났으므로 반건성유(半乾性油)로 인정(認定)되었다. 4) ester가(價)는 41.60이었다. 5) 수분(水分)은 11.28%로 나타났다. 6) 생송지(生松脂)의 불순물(不純物)은 0.06%였다. 7) turpentine oil의 함유량(含有量)은 23.26%로 나타났다. 8) rosin의 함량(含量)은 76.74%였다. 9) 수지산(樹脂酸)의 함량(含量)은 72.33%로 나타났다. 10) 생송지(生松脂) 중(中)의 불감화물은 4.41%였다. 11) 생송지(生松脂)의 굴절율(屈折率)은 $N^{20}_D$에서 1.5045로 측정(測定)되었다.

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제조방법에 따른 생강나무(Lindera obtusiloba BL.) 잎차의 향기 성분의 변화 (Changes on the Flavor Components in the Leaf Teas of Lindera obtusiloba BL. by Processing Methods)

  • 황경아;신승렬;김광수
    • 한국식품저장유통학회지
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    • 제12권1호
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    • pp.68-74
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    • 2005
  • 본 연구에서는 우리나라의 전통차의 계승과 새로운 식품의 개발하고자 생강나무의 잎을 이용한 차의 제조방법에 따른 향기성분의 변화를 조사하였다. 재차방법에 따른 향기성분은 덖음차 81종, 찐후덖음차 78종, 자연건조차 88종, 발효차 86종, 찐차 72종 및 인공건조차 89종의 분리할 수 있었다. 생강나무 잎차의 향기성분은 $\beta-piepne$을 비롯한 hydrocarbone류가 45종이 동정되었으며, 가장 많은 종류의 성분이 분포되었다. Alcohol류는 L-linalool, n-octanoal, phenyl acetaldehyde, $(-)-\alpha-terpineol$, elemol, cholest-5-en-3-ol, 등 16종, 2-nitro-2(3-hydroxybuthyl) -clododexanone, 3-(3-butenyl)-2,3-epoxy-cyclohexanone, 2-ethyl-2-propyl- cyclo-hexanone 등 11종의 ketone류가, phenyl acetaldehyde, tetradecanal, 10-undecanal, 4-Bromo-2- methylbutanal 등 8종의 aldehyde류가 동정되었다. 또한 ester류는 methyl 9, 12, 15-octadecatrienate, didodecyl phthalate, 1,2-benzenediccar-baboxy acid-bis(2-ethylhexyl) ester 3종류가 동정되었고, 또한 phenol류는 2,6-bis(1,1-dimethylethyl)-4-methyl-phenol이 동정되었다.

Amylase와 유화제의 첨가가 빵 반죽특성에 미치는 영향 (Effect of Amylase and Emulsifier on the Characteristics of the Bread Dough)

  • 박범준;황성연;박천석
    • 한국식품과학회지
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    • 제37권5호
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    • pp.763-767
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    • 2005
  • 본 연구에서는 곰팡이과 세균에서 유래된 ${\alpha}-amylase$와 유화제인 monogrlyceride(MG), sodium stearoyl-2-laclylate(SSL) 및 diacetyltartaric acid ester of monol and diglycerides(DATEM)을 첨가하여 반죽을 제조하고, 제빵 반죽의 물리적 특성인 falling number, farinogram, alvogram 및 RVA를 이용한 호화특성을 살펴보았다. ${\alpha}-amylase$의 전분분해로 인하여 falling number는 감소하였으나, MG를 혼합한 반죽의 경우 전분과 높은 결합력으로 falling number가 높게 나타났다. Farinogram 특성에서는 곰팡이와 세균에서 유래된 ${\alpha}-amylase$와 유화제가 반죽의 점탄성과 흡수율, 탄력도를 감소시키고, 흡수시간은 증가시켰다. 다만 유화세로 SSL+MG를 사용하였을 때, 대조구와 유사하거나 탄력도와 흡수시간이 더 높게 나타났다. Alveogram 특성에서는 farinogram과 유사하게 $P_{max}$ 값을 감소시켜 탄력도를 감소시켰으며, 신장성, 팽창성 및 탄력에 대한 저항성을 감소시켰다. 반죽의 호화특성에서는 호화개시온도에서는 ${\alpha}-amylase$와 유화제가 영향을 주지 않았으나, ${\alpha}-amylase$의 전분 분해로 인하여 반죽의 점도를 낮추는 경향을 보여주었다.

The inhibitory effects of 3,4,5-Trimethoxy cinnamate thymol ester(TCTE, Melasolv$\circledR$) on Melanogenesis

  • Hwang, Jae-Sung;Hyunjung Shin;Noh, Ho-Sick;Park, Hyunjung;Ahn, Soo-mi;Park, Dong-Soon;Kim, Duck-Hee;Lee, Byeong-Gon;Ihseop Chang
    • 대한화장품학회지
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    • 제28권1호
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    • pp.135-149
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    • 2002
  • To date, research on the regulation of melanogenesis has focused on factors which affect tyrosinase, the rate-limiting enzyme in the melanogenic pathway, by searching for chemicals which competitively inhibit tyrosinase function. Many types of tyrosinase inhibitors have been developed, but no satisfactory results have been made clinically until now, To find a new whitening agent, which effectively inhibits melanogenesis, we synthesized several compounds and selected compounds by cell-based assay system. Finally, 3, 4, 5-trimethoxy cinnamaie thymol ester(TCTE, Melasolv) was selected and the effects of TCTE on melanogenesis were investigated. Treatment of mouse-derived melanocyte melan-a cells with TCTE results in a marked down-regulation of tyrosinase activity. 80% decrease of tyrosinase activity occurs with 30uM TCTE treatment for 72 hours without affecting cell growth. The inhibition of tyrosinase activity is dose-dependent and melanin content was also decreased to 40%. From the in vitro tyrosinase assay using cell extract, TCTE does not act as a direct inhibitor of the enzyme. Treatment of melan-a cultures with TCTE blocks the increase in tyrosinase activity by either forskolin, 3-isobutyl-1-methtyl-xanthine. TCTE decreased the expression of tyrosinase, TRP-1 without effects on TRP-2 protein expression through the down regulation of tyrosinase and TRP-1 mRNA. From the results of cAMP immunoassays, intracellular levels of the cyclin nucleotide are unaffected in cells treated with TCTE. The inhibitory effects of melanin synthesis were also shown in reconstitute human epidermis model by topical application. These findings suggest that TCTE can be used for studying the regulation of melanogenesis and depigmenting agent.

바이오디젤의 산화 안정성 특성에 관한 고찰 (Review on the oxidation stability of biodiesel)

  • 이미은;황인하;김재곤;나병기
    • 한국응용과학기술학회지
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    • 제35권4호
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    • pp.1013-1030
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    • 2018
  • 바이오디젤은 동물성 유지, 식물성 유지와 그 부산물 등의 원료를 사용하여 지방산 메틸에스테르 형태로 제조된 연료이며, 석유계 에너지를 대체할 수 있는 바이오연료로 각광받고 있다. 그러나 바이오디젤은 저장 및 유통 과정에서 불포화 지방산 메틸에스테르가 산화되면서 연료의 품질이 저하되거나 자동차 엔진부품을 부식시키는 등의 문제를 일으킨다. 따라서 본 연구에서는 바이오디젤의 품질과 산화 특성이 산화 안정성에 미치는 영향을 알아보고, 이와 관련된 평가 방법에 대해 기술하였다. 또한 바이오디젤의 산화 안정성 단점을 개선할 수 있는 방안을 고찰하였다.

Four new cyclic peroxides from the Marine Sponge Plakortis simplex

  • Hwang, Buyng Su;Rho, Jung-Rae
    • 한국자기공명학회논문지
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    • 제17권1호
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    • pp.47-53
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    • 2013
  • Four new cyclic peroxide compounds (1~4) were isolated from the marine sponge Plakortis simplex. Their structures including relative stereochemistry were determined by MS and NMR analysis. All compounds, a side carbon chain with 10 carbons, were very unstable. After transformation into methyl ester analogues, the structure determination was conducted. Compounds 1a and 2a are stereoisomers, assigned as $3S^*$, $4S^*$, $6R^*$ and $3R^*$, $4S^*$, $6R^*$, respectively. Similarly, compounds 3a and 4a, replaced the methoxy group with an aliphatic methyl, are also stereoisomers. Compounds 1a and 2a exhibited the strong antifungal effect against the fungus Candida albicans.