• Title/Summary/Keyword: $\beta$-Pinene

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Monoterpenoid of Korean Valerian Roots (국산 길초근의 Monoterpenoid)

  • Ryu, Kyung-Soo
    • Korean Journal of Pharmacognosy
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    • v.5 no.1
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    • pp.1-6
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    • 1974
  • Essential oils were separated by steam distillation from the roots of four species of the genus Valeriana and subjected to gas chromatography to screen monoterpenic hydrocarbons and related components. The amounts of the common components were contained in the following order: camphene, ${\alpha}-pinene$, bornyl-, myrtenyl isovalerate, myrtenylacetate and ${\beta}-pinene$, and small amounts of terpineol and terpinylacetate were also contained. Of the four species, the root of Valeriana fauriei $B_{RIQUET}$ var. dasycarpa $H_{ARA}$ contained the largest amounts of these components and the root of V. dageletiana $N_{AKAI}$ ex $M_{AEKAWA}$ the least. Since the root of V. dageletiana contained for less amounts of pinene, camphene and bornylacetate and none of dipentene and terpineol, this plant appears to be distinguished from the other three species.

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Seasonal Variation of Monoterpenes in Artemisia Japonica Leaf (제비쑥(Artemisia japonica) 잎에서의 Monoterpenes의 계절적 변이)

  • 김종희
    • The Korean Journal of Ecology
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    • v.21 no.3
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    • pp.263-268
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    • 1998
  • The composition and concentration of monoterpenes in the leaves of Artemisia japonica were determined. And seasonal variation in monoterpenes of A. japonica were investigated. Samples were taken from five sites at Mt. Muhak. Monoterpenes in the leaves were analyzed using gas chromatography-mass spectrometry. The leaf monoterpene fractions were dominated by R.T. 5.026, ${\alpha}-thujene$, sabinene, ${\beta}-pinene$, cyclohexane (R.T.=12.859) and R.T. 23.149. There were marked seasonal differences in concentration and composition of leaf monoterpenes. There were many kinds of monoterpenes in leaf of spring time, however most of monoterpenes concentration was small. On the other hand, there were not many kinds of monoterpenes in late time, but monoterpene concentrations were increased.

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Autoxidation of Cycloalkenes by the System “Molecular Oxygen-bis(acetylacetonato) Cobalt (II) Complex-butyraldehyde”

  • Fang, Zhao;Tang, Rui-Ren;Zhang, Rui-Rong;Huang, Ke-long
    • Bulletin of the Korean Chemical Society
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    • v.30 no.10
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    • pp.2208-2212
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    • 2009
  • Oxidation of cycloalkenes with $O_2$ promoted by heterogeneous bis(acetylacetonato) cobalt (II) complex catalyst which can be recycled has been performed under mild conditions. It was found that $\beta$-ionone, cyclohexene, 1-methylcyclohexene, and $\alpha$-ionone were efficiently oxidized with $O_2$ in the presence of Co (II) complex and butyraldehyde at $55\;{^{\circ}C}$. A simple treatment of the resulting products led to epoxides as predominant products and a small amounts of allylic oxides, the chemoselectivity for the former being 82.1 - 90.8% with a 70.6 - 98.6% substrate conversion. On the other hand, oxidation of 1-phenylcyclohexene, 1-cyclohex-1-enylethan-1-one, $\alpha$-pinene, and $\beta$-pinene gave allylic oxides as major products.

Seasonal Variations of Monoterpene Concentrations in a Pine Forest in Florida, USA

  • Kim, Ki-Hyun;Kim, Jo-Chunn
    • Journal of Korean Society for Atmospheric Environment
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    • v.18 no.E3
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    • pp.175-180
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    • 2002
  • In order to study the distribution characteristics of natural volatile organic compounds (NVOCs), we investigated the seasonal variations of $\alpha$-and $\beta$-pinene levels in a pine forest in Florida for a you. The mean concentrations of $\alpha$- and $\beta$-pinene measured during the whole study period were computed to be 125: 86 (N = 65) and 86$\pm$52 pptv (N = 56), respectively. According to our data grouping scheme, the seasonal means for both pinones were observed to peak during fall with their max and min values in summer and winter, respectively. The overall results of our study suggest that terpenes are subject to highly strong temporal variability because of changes in their major source characteristics across seasons.

Isolation and Identification of Volatile Compounds extracted from Twigs of Pinus densiflora with Likens-Nickerson Apparatus (Likens-Nickerson 장치로 추출한 솔가지의 휘발성 성분의 분리 및 동정)

  • 이양봉;이미정;양지영;권혜순;윤정로
    • Journal of the Korean Society of Food Science and Nutrition
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    • v.27 no.4
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    • pp.568-573
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    • 1998
  • Volatile compounds in Pinus densiflora were extracted with Likens-Nickerson apparatus for three hours, and were separated and identified by gas chromatography(GC) and mass selective detector(MSD). Twenty six compounds were isolated from Pinus densiflora, identified by GC-MSD and twelve compounds were confirmed by matching retention times of the pure comounds. The main valatile compounds were terpenoids such as limonene(36.2%), $\beta$-pinene(16.9%), $\beta$-myrcene(12.6%) and $\alpha$-pinene(10.9%), and the total amount of these main compounds was 367.9$\mu\textrm{g}$ per 1g of pine twigs.

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Comparison of Major Monoterpene Concentrations in the Ambient Air of South Korea Forests

  • Oh, Gil-Young;Park, Gui-Hwan;Kim, Ik-San;Bae, Ju-Soon;Park, Hye-Young;Seo, Yun-Gyu;Yang, Soo-In;Lee, Joong-Ki;Jeong, Sun-Ho;Lee, Wan-Jin
    • Journal of Korean Society of Forest Science
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    • v.99 no.5
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    • pp.698-705
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    • 2010
  • The concentration of monoterpenes (12 species) was measured from spring to fall in 2008 in ambient air at six different forests located in the southern parts of Korea. Sampling - using a Solid Adsorption Tube - was conducted at 2-hour-interval a day (24 hours) of each season. The highest annual average concentration of total monoterpene was 0.715 ppbv, which occurred at Mt. Baega. ${\alpha}$-Pinene, sabinene and ${\beta}$-pinene were the most abundant compounds throughout the sampling periods and areas. The concentrations of monoterpene were higher in spring than in any other seasons. The compositions and concentrations of monoterpene displayed a distinct pattern by area. Most of monoterpenes had diurnal variations with higher concentrations during the daytime, and lower during the nighttime. This may be due to the fact that the amount of monoterpenes emitted increases at elevated ambient temperatures and increased sunlight intensity. The results of this study showed that each area had distinct monoterpene compositions, which depended on the tree species, topography and local climate at each area.

Changes in terpenes of three kinds of pine needles during litter decomposition

  • Jo, Gyu-Gap;Kim, Jong-Hee
    • Journal of Ecology and Environment
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    • v.33 no.2
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    • pp.175-186
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    • 2010
  • This study was designed to evaluate changes in the terpene composition of 3 types of pines (Pinus densiflora, Pinus thunbergii and Pinus rigida), while decomposing their leaf litter. Needle litters were placed at two different organic layer depths, one on the surface and the other beneath the litter layer. Changes in the terpene composition of this litter were detected using a gas chromatograph-mass spectrometer. Among the monoterpenes acquired from the fresh needles of P. densiflora and P. rigida, $\alpha$-pinene (12.05% and 19.87%, respectively) was the major one, followed by $\beta$-pinene (2.90% and 14.07%). However, from the needles of P. thunbergii, $\beta$-pinene (20.77%) was the major one, followed by $\alpha$-pinene (10.79%). Among the sesquiterpenes detected in P. densiflora, trans-caryophyllene (3.12%) was the highest composition compound, whereas germacrene-D (6.09%) for P. thunbergii and 1,6-cyclodecadiene (7.41%) and endo-1-bourbonanol (7.41%) for P. rigida were the highest content compounds. However, the total amounts of terpenes decreased sharply by 40-85.4% in all three types of pine needle after 90-120 days of the experiment. The concentration of each terpene differed during decomposition, and the majority of compounds disappeared from beneath the litter layer. It was determined that three types of reducing patterns of each compound appeared on the rate of loss of concentration during decomposition; one pattern decreasing sharply during the initial period, another pattern steadily or slowly decreasing, and a newly detected pattern at low concentration occurring during decomposition.

Analysis of Volatile Flavor Components of Aster glehni (섬쑥부쟁이의 휘발성 향미성분 분석)

  • 이미순;정미숙
    • Korean journal of food and cookery science
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    • v.14 no.5
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    • pp.547-552
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    • 1998
  • Essential oils in leaf of fresh Aster glehni were extracted by SDE (simultaneous steam distillation and extraction) method using diethyl ether as solvent. The yield of the essential oils was 0.05%. And their volatile flavor components were analyzed by gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS) and identified by the RI of GC and mass spectrum of GC-MS. A total of 31 components, including 17 hydrocarbons, 2 aldehydes, 7 alcohols, 3 esters, 1 acid and 1 oxide were identified. The major volatile flavor components of fresh Aster glehni were ${\alpha}$-pinene, limonene, $\delta$-elemene, ${\beta}$-pinene, cis-3-hexenol and myrcene. Volatile flavor patterns of fresh ind dried Aster glehni were analyzed using an electronic nose. Sensor PA2 that was sensitive to alcohols showed the highest resistance for fresh and dried Aster glehni. Resistance of six metal oxide sensors was decreased in fresh sample compared with dried one.

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Studies on the Volatile Flavor Components of Spices in Curry (향신료의 휘발성 향미성분에 관한 연구)

  • Kim, Hyean-Wee;Huh, Kyung-Taek;Choi, Chun-Un
    • Korean Journal of Food Science and Technology
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    • v.21 no.1
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    • pp.127-135
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    • 1989
  • The volatile components of nutmeg, cumin, cardamon, turmeric, coriander, clove, allspice, cassia, fennel, celery seed and black pepper, having a characteristic spicy aroma and being used as an ingradient of curry powder, were investigated. After steam distillation followed by extraction with diethyl ether: n-pentane(2:1, v/v) mixture, the volatile components were identified by capillary GC and GC/MS. As a result, following major compounds were identified. ${\alpha}-pinene(11.06%)$, ${\beta}-pinene(11.17%)$ and myristicin(19.98%) in nutmeg, cuminaldehyde(37.68%) in cumin, ${\alpha}-terpineol(47.33%)$ and 1, 8-cineol(20.56%) in cardamon, linalool(61.72%) in coriander, eugenol(63.63%) and eugenol acetate(20.59%) in clove, eugenol(80.12%) and methyl eugenol(10.85%) in allspice, cinnamaldehyde(82.29%) in cassia, anethole(79.92%) in fennel.

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Emission Characteristics of VOCs in Drying Process for Plywood Manufacturing (합판 제조용 목재 건조공정에서의 휘발성 유기화합물(VOCs) 배출특성)

  • Jang, Jeong-Gook;Kim, Mi-Ran
    • Journal of Environmental Science International
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    • v.17 no.12
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    • pp.1381-1390
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    • 2008
  • Emission characteristics of volatile organic compounds (VOCs) were investigated in the flue gas emitted from wood drying process for plywood manufacturing. The moisture content of raw timber was average 48%, and its density was $831.55kg/m^3$. But the moisture content of dried wood is needed less than around 10%, thus the moisture contents of flue gas should be remarkably high(about 18.2 V/V%). Therefore, the vapor in flue gas is equivalent to 320 ton-vapor/day when 1100 ton-wood/day is treated in the wood drying process. The temperature of flue gas ranges from $140^{\circ}C\;to\;150^{\circ}C$ in each dryer stack with exception of the input site of wood(about $110^{\circ}C$). The velocity of flue gas in each stack ranges from 1.7 to 9.7m/sec. In order to assess the concentrations and attribution rate of odorous compounds, it was analyzed about 40 VOCs in the flue gases. It was found that the major odorous compounds were 8 compounds, and the concentrations of major VOCs(ppm) were as follows; benzene: $0.054{\sim}0.052$, toluene: $1.011{\sim}2.547$, ethylbenzene: $0.472{\sim}2.023$, m,p-xylene: $0.504{\sim}3.245$, styrene: $0.015{\sim}0.148$, o-xylene : $0.271{\sim}1.097$, ethanol: $11.2{\sim}32.5$, ${\alpha}$-pinene: $0.908{\sim}10.578$, ${\beta}$-pinene: $0.982{\sim}14.278$. The attribution rate of terpenes (${\alpha}$-pinene, ${\beta}$-pinene) was about 60.56%, and that of aromatics and alcohols was about 22.77%, and 16.67%, respectively. It is suggested that the adequate control device should be used to control both the water soluble and non-soluble compounds because both compounds were mixed in flue gas.