• 제목/요약/키워드: Molar extinction coefficient

검색결과 21건 처리시간 0.025초

Determination of some useful radiation interaction parameters for waste foods

  • Akman, F.;Gecibesler, I.H.;Sayyed, M.I.;Tijani, S.A.;Tufekci, A.R.;Demirtas, I.
    • Nuclear Engineering and Technology
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    • 제50권6호
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    • pp.944-949
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    • 2018
  • The mass attenuation coefficients (${\mu}/{\rho}$) of food waste samples (pomegranate peel, acorn cap, lemon peel, mandarin peel, pumpkin peel, grape peel, orange peel, pineapple peel, acorn peel and grape stalk) have been measured employing a Si(Li) detector at 13.92, 17.75, 20.78, 26.34 and 59.54 keV. Also, the theoretical values of the mass attenuation coefficients have been evaluated utilizing mixture rule from WinXCOM program. The results showed that the lemon peel has the highest values of ${\mu}/{\rho}$ among the selected samples. From the obtained mass attenuation coefficients, we determined some absorption parameters such as effective atomic number ($Z_{eff}$), electron density ($N_E$) and molar extinction coefficient (${\varepsilon}$). It was found that the $Z_{eff}$ values of all food wastes lie within the range of 4.034-7.595, whereas the $N_E$ of the studied food wastes was found to be in the range of $0.301-1.720{\times}10^{25}$ (electrons/g) for present energy region.

띠미로버섯 중 25-Epi, $3{\alpha}-Carboxyacetylquercinic$ Acid의 분리정제, 구조결정 및 생리활성 (Isolation, Structure Determination and Biological Activity of 25-Epi, $3{\alpha}-Carboxyacetylquercinic$ Acid in Daedalea dickinsii)

  • 배강규;민태진
    • 대한화학회지
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    • 제44권1호
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    • pp.37-44
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    • 2000
  • 띠미로버섯의 에탄올 추출물 중 25-Epi, $3{\alpha}-carboxyacetylquercinic$ acid의 두 구조, 항균활성 및 항암활성을 연구하였다. 화합물 1의 녹는점과 분자량은 각각 $167{\sim}168^{\circ}C$, 572였고, 몰 흡광 계수는 208 nm에서 5,040이었다. 여러 분광학적 성질로부터 이는 24S, 25S, $3{\alpha}-carboxyacetylquercinic$ acid로 확인되었고, 곰팡이, 효모 및 세균들에 대한 항균활성과 항암활성($IC_{50}=64.5\;{\mu}M$)이 있었다. 화합물 2의 녹는점, 분자량 및 몰흡광 계수는 각각 $233{\sim}235^<\circ}$, 572 및 208 nm에서 5,080이었다. 이는 24S, 25R, $3{\alpha}-carboxyacetylquercinic$ acid로 확인되었고, 화합물 1과 서로 다른 항균활성을 보였다.

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1-Isonicotinoyl-2-furfurylidene Hydrazine-Cu(II) 착화합물에 관한 분석화학적연구 (Studies on 1-Isonicotinoyl-2-furfurylidene hydrazine-Cu(II) Complex Compound.)

  • 백남호;최윤수
    • 약학회지
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    • 제9권1_2호
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    • pp.18-22
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    • 1965
  • A new organic reagent, 1-isonicotinoyl-2-furfurylidene hydrazine was synthesized from isonicotinic acid hydrazide and furfural, gives precipitate with copper(II), mercury(II) and argent(I), whereas, it gives a water soluble yellow complex with iron(III). Copper complex of the reagent is soluble in EtOH MtOH, pyridine, dioxane and dimethylformamide with green yellow coloration. The complex has a maximum absorption at 385 m.$\mu$ and molar ratio of copper; reagent was estimated as 1:1 by continuous variation method, slop method and chelate titration method. Molar extinction coefficient (9600) and apparant formation constant of this complex was spectrophotometrically determined. K=1.7 * $10^{7}$ (Babko's method) K=2.1 * $10^{7}$ (Anderson's method). This reagent reacted with copper so sensitive that it would be available for determination of Cu (II).

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재사용이 가능한 MFB로부터 Aromatic Ester가 도입된 4,4'-Di((E)-styryl)-1,1'-biphenyl의 골격을 갖는 새로운 Fluorescent Whitening Agent의 개발 연구 (Development of New Fluorescent Whitening Agent with 4,4'-Di((E)-styryl)-1,1'-biphenyl Skeleton Attached with Aromatic Ester from Recyclable Source MFB)

  • ;김석찬
    • 공업화학
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    • 제29권3호
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    • pp.303-306
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    • 2018
  • DMT 생산과정의 부산물로서 폐기 처리되어 왔던 methyl 4-formylbenzoate (MFB)를 출발 물질로 하여 고급 형광 증백제 family와 동일한 4,4'-di((E)-styryl)-1,1'-biphenyl 기본 골격을 갖고 aromatic ester가 도입된 새로운 형광 증백제(fluorescent whitening agent) 후보 물질 6종을 합성하였다. 후보 물질 6종은 MFB 및 그의 유도체와 tetraethyl biphenyl-4,4'-diylbis(methylene)diphosphonate와 Wittig-Horner 반응을 이용하여 합성하였다. 합성된 6종에 대하여 형광증백제로의 가능성을 확인하기 위하여 UV 스펙트럼을 기록하여 흡광 계수를 얻었으며, 6종 모두 전반적으로 기존 상용 제품(log ${\varepsilon}$ 4.85)과 유사한 몰 흡광 계수(log ${\varepsilon}$ 4.59~5.00)를 보여주고 있다. 특별히 화합물 디메톡시 페닐그룹을 갖는 16, 17은 기존 상용 제품보다 우수한 몰흡광 계수를 나타내고 있어 상용화를 위한 현장 테스트를 진행할 예정이다.

순수 폴리프로필렌 섬유용 알킬치환 안트라퀴논계 염료의 색상발현 특성 (The Coloration Properties of Alkyl-substituted Anthraquinoid Dyes for Pure Polypropylene Fiber)

  • 김태경;정종석;윤석한;김미경;손영아
    • 한국염색가공학회지
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    • 제19권6호
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    • pp.28-34
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    • 2007
  • The optical and physical properties of alkyl-substituted anthraquinoid dyes were investigated in terms of dyeing of pure polypropylene fiber. The length of alkyl substituents of the dyes did not affect the molar extinction coefficient and maximum absorption wavelength of them. The use of a double-tailed cationic surfactant, didodecyldimethylammonium bromide(DDDMAB), could make the hydrophobic dyes dispersed in water effectively. As the amount of DDDMAB increased, the average particle size of dye dispersion decreased. Maximum color strength of the fabrics was shown in the case that 1.5 molar ratio of DDDMAB was used. As for the fastness properties, commercially acceptable result was obtained in general.

Relation between Chemical Structure of Yellow Disperse Dyes and Their Lightfastness

  • Kim, Sung-Dong;Park, Eun-Jin
    • Fibers and Polymers
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    • 제2권3호
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    • pp.159-163
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    • 2001
  • Five yellow disperse dyes were synthesized and their dyeing, fastness and photodegradation behaviors were investigated. It was found that dyes derived from phenylindole and N-alkylaminobenzene showed dye uptake directly proportional to the dye concentration, but the build-up of dyes derived from carbazole and pyridone were not good. The wavelength at maximum absorption. molar extinction coefficient. and the tendency to the photodegradation were strongly dependent on the electron donating ability of the coupling component. The dye, whose coupling component was phenylindole, possessed the excellent dyeing properties and the high degree of lightfastness. UVA had an effect on the inhibition of the photodegradation especially for the easily photodegradabte dyes.

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수용성 치자 색소의 추출에 관한 연구 (A Study on the Extraction of Soluble Colorants of the Gardenia jasminoides Ellis)

  • Kim, Kwang Soo;Kim, Yeon Joong
    • 한국염색가공학회지
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    • 제9권3호
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    • pp.10-17
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    • 1997
  • The study was performed to obtain the optimum extraction conditions for crocin from gardenia fructus. Generally crocin is unstable on heat, light, acid and base solution. The extraction efficiency of crocin from gardenia depended upon the extraction time, extraction temperature, pH in the extraction bath and the optimum conditions of crocin extraction were determined as 60 minutes of extraction time, 4$0^{\circ}C$ of extraction temperature, pH 7 of extraction bath. The molar extinction coefficient of crocin was 12,515 and the color yield of purified crocin was about six times higher than that of non-purified crocin. The heat-stability at extraction temperature and lightstability in irradiation with xenon lamp for one hour of the purified crocin were higher than those of non-purified crocin. Intensity of &{\lambda}_{max}&of crocin was decreased by irradiation for one hour but UV-Vis. spectra of crocin was not changed. The colors of purified and non-purified crocin dissolved wit methanol was evaluated by means of CIE L* a* b* system.

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페노시아진을 이용한 염료감응형 태양전지 고효율 염료합성 (Synthesis and Photovoltaic Properties of Organic Photosensitizers for Application of Dye Sensitized Solar Cells)

  • 양현식;신소연;김연지;김재홍
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2011년도 춘계학술대회 초록집
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    • pp.119.2-119.2
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    • 2011
  • Dye-sensitized solar cells (DSSC) are currently attracting wide spread academic and commercial interest for the conversion of sunlight into electricity because of their easy manufacturing process and high efficiency. The solar energy conversion efficiencies of DSSC are strongly dependent on dye molecules adsorbed on the TiO2 surface which used for photosensitization of sun light, since an excited state of dye could inject an electron into the conduction band of semiconductor. We have developed novel organic dyes which have phenothiazine moieties as an electron donor in their charge-transfer chromophore for application of DSSCs. We had synthesized a series of phenothiazine derivatives which have different wave length absorbing chromophore in the molecule with high molar extinction coefficient. The photovoltaic performance of DSSC composed of organic chromophores with broad wavelength absorption property were measured and evaluated by comparison with that of pristine ruthenium dye.

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1-isonicotinyl-2-furfurylidene hydrazine-Cd(II) 착화합물에 관한 분석화학적연구 (Spectrophotometric study of the cadmium (II) complex of 1-isonicotinyl-2-furfurylidene hydrazine)

  • 백남호;박만기
    • 약학회지
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    • 제13권1호
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    • pp.33-37
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    • 1969
  • A new organic reagent, 1-isonicotynyl-2-furfurylidene hydrazine synthesized from isonicotinic acid hydrazid and furfural, gives yellow liquid with cadmium (II). Cadmium complex of the reagent is soluble in water with yellow coloration. The complex has a maximum absorption at 363 m${\mu}$ and molar ratio of cadmium to reagent was estimated as 1:1 by continuous variation method and slope method. Molecular extinction coefficient and apparent formation constant of this complex was spectrophotometrically determined. K=4.48 $\times$ 10$^{3}$ (Babko's method) K=1.33 $\times$ 10$^{3}$ (Anderson's method)

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Purification, Structure Determination and Biological Activities of 20(29)-lupen-3-one from Daedaleopsis tricolor(Bull.ex Fr.)Bond.et Sing.

  • 김은미;정해룡;민태진
    • Bulletin of the Korean Chemical Society
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    • 제22권1호
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    • pp.59-62
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    • 2001
  • The dried fruit-body of Daedaleopsis tricolor was extracted by the petroleum ether. The extracts were purified by liquid-liquid extraction, column chromatography, and recrystallization. The purified compound was a colorless orthorhombic crystal form. Its melting point, molecular weight and molar extinction coefficient $(\varepsilon)$ were estimated $168-170^{\circ}C$, 424 and 3,935 at 208 nm, respectively. Its structure was elucidated to be 20(29)-lupen-3-one by UV-Vis, FT-IR, NMR and X-ray crystallographic analysis. It showed antifungal activities against Saccharomyces cerevisiae and Microsporum gypseum, and antibacterial activities against Escherichia coli, Proteus vulgaris, Pseudomonas pyocyanea, Bacillus subtilis, and Staphylococcus aureus. In addition, this compound showed an antioxidative activity on lipid-peroxidation by 6.4%.