• 공업화학
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• 제10권5호
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• pp.666-671
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• 1999

본 연구에서 술폰화된 poly(phenylene sulfide)(SPPS)는 10%의 발연황산으로 PPST를 술폰화한 후 NaOH 수용액으로 demethylation하여 제조하였다. 유기용매에 용해되는 PPST는 methyl-(phenylthio)phenyl sulfoxide(MPPSO)의 자가축합 반응으로 합성되었다. SPPS는 $1200cm^{-1}$에서 $-SO_{3}H$의 비대칭 O=S=O 신축진동에 의한 흡수피크와 $621cm^{-1}$에서 S-O 신축진동에 의한 흡수피크가 관찰된 것으로 보아 술폰산기가 도입된 것을 알 수 있다. PPST의 술폰화를 $150^{\circ}C$에서 12시간 반응했을 때 반복단위당 1.48개의 술폰산기가 도입되었으며, 고온 GPC로 측정된 PPST와 SPPS의 중량평균분자량(Mw)은 각각 118323과 131204이었다. SPPS의 암모니아 가스 흡착능은 $9.67mmol\;NH_{3}/g$이었고, 활성탄, 실리카겔보다 월등히 높았다.

• 한국건설순환자원학회논문집
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• 제6권2호
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• pp.108-114
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• 2018

콘크리트 구조물은 사용기간 동안 표면 열화 및 오염으로 인해 미관의 저하 및 내구성 저하가 발생된다. 최근 들어 광촉매(photocatalyst)를 이용하여 유기산화물을 제거하고 표면자기정화(self cleaning) 성능을 개선하려는 연구가 시도되고 있다. 본 논문은 실리케이트 기반 광촉매 함침을 위한 기초연구로서 CS와 SC 두 가지 함침 용액을 대상으로 하였다. 실리케이트 기반 용액의 점성과 표면장력을 평가하였으며 콘크리트에 적용하여 부착강도를 평가하였다. 또한 실리케이트 용액에 침지된 콘크리트에 대하여, 광촉매 용액의 침지 및 분무를 한 후 콘크리트 강도 평가와 SEM을 통한 표면상태를 조사하였다. 실리케이트 용액의 침지 후 30분간 기건 상태를 유지하고 분무하는 방법이 가장 효과적으로 광촉매의 표면 흡착을 유도하는 것으로 평가되었으며, 강도 개선에도 효과적임을 알 수 있다.

• Journal of the Korean Wood Science and Technology
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• 제41권4호
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• pp.269-275
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• 2013

본 연구는 유기질 문화재 보존을 위해 한국 전통 약용식물을 대상으로 항균 및 살충활성을 검증한 결과 황벽나무 열매 추출물이 우수한 활성을 나타냄을 확인하였다. 황벽나무 열매 추출물을 비극성 용매로 분획하여 그 중 가장 활성이 우수한 ethylacetate 분획물을 대상으로 실리카젤 및 Sephadex LH-20 컬럼 크로마토그래피를 실시하고 Prep-TLC를 이용하여 화합물을 순수 분리하였다. 화합물은 UV spectrum 분석 결과 260 nm 파장에서 최대흡수피크가 관찰되었고, $^1H$, $^{13}C$, HMQC, HMBC NMR과 ESI mass spectrum을 이용하여 화학구조를 분석한 결과 (4'-ethyl-2'-methylfuranyl)-6-methoxy-7-methylnona-2E,4E,6Z,8E-tetraenoic acid의 새로운 화합물임을 알 수 있었다.

• 분석과학
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• 제16권2호
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• pp.166-173
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• 2003

HRGC/ECD를 이용한 congener specific analysis 방법으로 국내 유통식품 중 PCBs의 오염실태를 조사하였다. Indicator PCB인 IUPAC #28, #52, #101, #118, #138, #153 및 #180 7종을 대상물질로 하였으며, 소고기, 돼지고기, 닭고기, 계란, 고등어, 조기, 멸치, 오징어, 바지락을 대상시료로 선정하여 서울, 부산, 광주 3개 지역에서 수집하였다. 채취한 시료는 균질화하여 알칼리 분해후 유기용매로 추출하여 지방을 분해하고 실리카겔 컬럼으로 정제하여 dual column-HRGC/ECD로 분석하였으며 검출된 시료에 대해서는 HRGC/MSD로 재확인하였다. 분석결과 고등어 등 어류 시료에서 미량수준 (0.0002~0.001 mg/kg)의 PCBs가 검출되었으며 주요 검출물질은 PCB #101과 PCB #118이었다.

• Journal of Microbiology and Biotechnology
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• 제10권2호
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• pp.251-257
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• 2000

Chitin synthases are identified as key enzymes of chitin biosynthesis in most of the fungi. Among them, chitin synthase II has been reported to be and essential enzyme in chitin biosynthesis, and exists as a membrane-bound form. To search and screen new antifungal agents from natural resources to inhibit chitin synthase II, the assay conditions were established using the enzyme isolated from Saccharomyces cerevisiae ECY38-38A(pAS6) that overproduces only chitin synthase II. This enzyme was activated only by partial proteolysis with trypsin. Its actibity reached the maximum at $80{\;}\mu\textrm{g}/ml$ of trypsin and was strongly stimulated by 2.0 mM $Co^{2+}$, 1.0 nM UDP-[$^{14}C$]-GicNAc, and 32 mM free-GlcNAc. Under these assay conditions, the highest chitin synthase II activity was observed by incubation at $30^{\circ}C$ for 90 min. However, and extremely narrow range of organic solvents up to as much as 25% of DMSO and 25% of MeOH was useful for determining optimal assay conditions. After a search or potent inhibitors of chitin synthase II from natural resources, prodigiosin was isolated from Serratia marcescens and purified by solvent extration and silica gel column chromatographies. The structure of prodigiosin was determined by UV, IR, Mass spectral, and NMR spectral analyses. Its molecular weight and formula were found to be 323 and $C_{20}H_{25}N_{3}O$, respectively. Prodigiosin ingibited chitin synthase II by 50% at the concentration of $115{\;}\mu\textrm{g}/ml$.

• 상하수도학회지
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• 제9권3호
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• pp.99-107
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• 1995

Various humic substances are widely distributed in natural water body, such as rivers and lakes and cause the yellowish or brownish color to water. The evidence that humic substances are precursors of THMs formation in chlorinated drinking water has been reported m the Jiteratures. For the reason of public health as well as aesthetics, needs for humic substances removal have been increased in the conventional water treatment processes. In this research, the characteristics of aluminium coagulation of humic acids and humic acids were investigated. The optimum pH and coagulants dosage to remove these materials simultaneously by coagulation were alto studied. The results are as followed; 1. UV-254 absorptiometry for measuring the concentration of aquatic humic acids showed good applicability and stable results. 2. The optimal pH range for humic acids removal by aluminium coagulation was 5 to 5.5, however, an increase in aluminium coagulant dosage could enhance the removal rate of humic acids in the wide pH range. 3. Coprecipitation of humic acids in the typical pH range of 6.5 to 8 in water treatment processes may require the sweep coagulation mechanism with the excess aluminium coagulant dosage. 4. Using PAC(poly aluminium chloride) or PASS(poly aluminium silica sulfate) as coagulants was able to expand the operating range for removing humic acids. 5. From the coagulation of humic substances(UV-254) and turbidity at pH range of 5.5 - 6.0 and alum dose of 86 ppm, the removal efficiency of turbidity from the reservoir water was above 90% and that of UV-254 was above 70%. 6. By using the reservoir water, the optimum condition of rapid mixing for simultaneous removal of turbidity and UV-254 absorbance was pH of 5.8 and LAS dose of 86 ppm, in this study.

• Bulletin of the Korean Chemical Society
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• 제32권8호
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• pp.2765-2770
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• 2011

Organic dye-doped glasses, viz., ruthenium (II) tris(4,7'-diphenyl-1,10'-phenanthroline) $[Ru(dpp)_3]^{2+}$ incorporated into thin silica xerogel films produced by the sol-gel method, were prepared and their $O_2$ quenching properties investigated as a function of the $[Ru(dpp)_3]^{2+}$ concentration (3-400 ${\mu}M$) within the xerogel. The ratio of the luminescence from the $[Ru(dpp)_3]^{2+}$-doped films in the presence of $N_2$ and $O_2$ ($I_{N2}/I_{O2}$) was used to describe the film sensitivity to $O_2$ quenching. ($I_{N2}/I_{O2}$ changed three-fold over the $[Ru(dpp)_3]^{2+}$ concentration range. Time-resolved intensity decay studies showed that there are two discrete $[Ru(dpp)_3]^{2+}$ populations within the xerogels (${\tau}_1$ ~ 300 ns; ${\tau}_2$ ~ 3000 ns) whose relative fraction changes as the $[Ru(dpp)_3]^{2+}$ concentration changes. The increased $O_2$ sensitivity that is observed at the higher $[Ru(dpp)_3]^{2+}$ concentrations is a manifestation of a greater fraction of the 3000 ns $[Ru(dpp)_3]^{2+}$ species (more susceptible to $O_2$ quenching). A model is presented to describe the observed response characteristics resulting from $[Ru(dpp)_3]^{2+}$ distribution within the xerogel.

• 한국입자에어로졸학회지
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• 제12권3호
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• pp.65-72
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• 2016

Nanoporous $SiO_2$ particles containing different pore volume and size were prepared from silicic acid by a spray pyrolysis. The pore size, pore volume and particle size could be controlled with varying the precursor concentration, reaction temperature, and amount of organic templates such as Urea and poly ethylene glycol (PEG). The pore size distribution, pore volume and specific surface area of as-prepared particles were analyzed by BET and BJH methods, and the average particle sizes were measured by a laser diffraction method. The nanoporous $SiO_2$ particles ranged $0.6-0.9{\mu}m$ in diameter were successfully synthesized and the average particle size increased as the silicic acid concentration increased. The morphology of nanoporous $SiO_2$ particles was spherical and pores ranged 1 - 40 nm in diameter were measured in the particles. In case of Urea added into silicic acid, it showed no much difference in the morphology, pore size and pore volume at different Urea concentration. On the other hand, when PEG was added, it was clearly observed that pore diameter and pore volume of the particles surface increased with respect to PEG concentration.

• Asian-Australasian Journal of Animal Sciences
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• 제12권7호
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• pp.1049-1053
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• 1999

Chopped wheat straw (0.5-1.5 cm) was subjected to different treatment combinations in a $5{\times}4$ factorial arrangement involving the five levels of urea (0, 2, 3, 4 and 5%, w/w) and four levels of lime (0, 2, 4 and 6%, w/w) at 50% moisture and kept for 3 wk reaction period at about $35{^{\circ}C}$ in laboratory. Treated wheat straw samples were analyzed to study the associative effect of urea and lime on chemical composition, in sacco and in vitro digestibilities. Results showed that cell wall constituents (CWC) solubilized significantly (p<0.01) due to urea and lime treatment on one hand and substantially increase the crude protein (CP) on the other in wheat straw. The main effect on synergism of both chemicals was noticed on organic matter (OM), neutral detergent fibre (NDF), hemicellulose (HC), acid detergent lignin (ADL) and silica by solubilising their contents as a result of considerable increase in cell contents in treated wheat straw. The respective decreases were 5.45, 13.0, 37.23, 44.95 and 26.16% in different treatment combinations. The most interesting feature of the treatment was evident by increase in ash content on each level of lime application. CP content increase up to 12.78% due to urea treatment in comparison with untreated wheat straw (2.56%). The effect of solubilization of structural carbohydrates and increased crude protein due to synergistic effect of urea and lime were clearly seen on improved digestibility of OM and DM. The increase in ISOMD, ISDMD, and IVDMD were 21.67, 21.67, 16.24, and 17.5 units. The increase in digestibility were relative to additions of both chemicals and digestibility values increased with increasing levels of urea plus lime concentration in different treatment combination. The maximum improvement was noticed at 4% urea and 4% lime levels at 50% moisture for 3 wk reaction period in treated wheat straw.

• Archives of Pharmacal Research
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• 제26권4호
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• pp.279-285
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• 2003

In our ongoing study to identity antioxidants from natural sources, the antioxidant activity of Nelumbo nucifera stamens was evaluated for their potential to scavenge stable 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radicals, inhibit total reactive oxygen species (ROS) generation, in kidney homogenates using 2 ,7 -dichlorodihydrofluorescein diacetate (DCHF-DA), and scavenge authentic peroxynitrites ($ONOO^-$). A methanol (MeOH) extract of the stamens of N. nucifera showed strong antioxidant activity in the $ONOO^-$system, and marginal activity in the DPPH and total ROS systems, so were therefore fractionated with several organic solvents, such as dichloromethane ($CH_2 Cl_2$), ethyl acetate (EtOAc) and n-butanol (n-BuOH). The EtOAc soluble fraction, which exhibited strong antioxidant activity in all the model systems tested, was further purified by repeated silica gel and Sephadex LH-20 column chromatographies. Seven known flavonoids [kaempferol (1), kaempferol 3-Ο-$\beta$-D-glucuronopyranosyl methylester (2), kaempferol 3-Ο-$\beta$-D-glucopyranoside (3), kaempferol 3-Ο-$\beta$-D-galactopyranoside (4), myricetin 3 ,5 -dimethylether 3-Ο-$\beta$-D-glucopyranoside (5), kaempferol 3-Ο-$\alpha$-L-rhamnopyranosyl-(1$\rightarrow$6)-$\beta$-D-glucopyranoside (6) and kaempferol 3-Ο-$\beta$-D-glucuronopyranoside (7)], along with $\beta$-sitosterol glucopyranoside (8), were isolated. Compound 1 possessed good activities in all the model systems tested. Compounds 2 and 7 showed scavenging activities in the DPPH and $ONOO^-$ tests, while compounds 3 and 4 were only active in the $ONOO^-$ test. Conversely, compound 8 showed no activities in any of the model systems tested.