• Title/Summary/Keyword: $\delta$ $^{15}N$

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Excess Volumes, Speeds of Sound, Isentropic Compressibilities and Viscosities of Binary Mixtures of N-Ethyl Aniline with Some Aromatic Ketones at 303.15 K

  • Gowrisankar, M.;Sivarambabu, S.;Venkateswarlu, P.;Kumar, K. Siva
    • Bulletin of the Korean Chemical Society
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    • v.33 no.5
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    • pp.1686-1692
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    • 2012
  • Densities (${\rho}$), Viscosities (${\eta}$) and ultrasonic speeds (u) of pure acetophenone (AP), propiophenone (PP), $p$-methyl acetophenone ($p$-MeAP), $p$-chloroacetophenone ($p$-ClAP) and those of their binary mixtures with $N$-ethyl aniline ($N$-EA) as a common component, were measured at 303.15 K over the entire composition range. These experimental data were used to calculate the excess volume $V^E$, deviation in ultrasonic speeds ${\Delta}u$, isentropic compressibility $K_s$, intermolecular free length $L_f$, acoustic impedance Z, deviations in isentropic compressibility ${\Delta}K_s$, deviation in viscosity ${\Delta}{\eta}$ and excess Gibbs free energy of activation of viscous flow ($G^{*E}$) at all mole fractions of $N$-ethyl aniline. These parameters, especially excess functions, are found to be quite sensitive towards the intermolecular interactions between component molecules. Theoretical values of viscosity of the binary mixtures were calculated using different empirical relations and theories. The relative merits of these relations and theories were discussed. The experimental results were correlated by using the polynomial proposed by Redlich-Kister equation.

Near-IR Spectroscopic Studies of the Hydrogen Bonding Between Thiopropionamide and N,N-Dimethylalkylamide in Carbon Tetrachloride (사염화탄소 중에서 Thiopropionamide와 N,N-Dimethylalkylamide사이의 수소결합에 관한 분광학적 연구)

  • Byung-Chul Kim;Chang-Ju Yoon;Kyuseok Song;Young Sang Choi
    • Journal of the Korean Chemical Society
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    • v.33 no.2
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    • pp.156-163
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    • 1989
  • The $ν_a+amide II$ combination band of thiopropionamide has been recorded for investigation of Hydrogen bonding between thiopropionamide (TPA) and N,N-dimethylalkylamide (DMF, DMA and DMP) in carbon tetrachloride over the range of $5^{\circ}$ to $55^{\circ}$. The combination band of monomeric TPA and hydrogen-bonded TPA can be resolved by Lorentzian-Gaussian product function into monomeric TPA and hydrogen-bonded TPA with amides. The association constants ($K_1$) for the hydrogen-bonded TPA were calculated by the concentrations of the monomeric TPA and the hydrogen-bonded TPA obtained from the computer resolved absorption bands. Thermodynamic parameters for the Hydrogen bonding have been evaluated by the analysis of the temperature dependent spectra. The ${\Delta}$$H^{\circ}$ of hydrogen-bonded TPA with DMF, DMA and DMP have been found to be-12.5, -13.5 and -14.1 kJ/mol, respectively. The corresponding ${\Delta}$$S^{\circ}$for the above system were -15.2, -17.9 and -22.3 J/mol${\cdot}$deg, respectively.

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Near-IR Spectroscopic Studies of the Hydrogen Bonding between Thioacetamide and N,N-Dimethylacetamide in $CCl_4$ ($CCl_4$중에서 Thioacetamide와 N,N-Dimethylacetamide사이의 수소 결합에 관한 분광학적인 연구)

  • Kang Bong Lee;Byung-Chul Kim;Chang-ju Yun;O. D. Bonner;Young-Sang Choi
    • Journal of the Korean Chemical Society
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    • v.30 no.6
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    • pp.510-515
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    • 1986
  • Spectra for the $v_3$+ Amide II combination band of thioacetamide(TA) were obtained in carbon tetrachloride solutions and in very dilute solutions of TA-N,N-dimethlylacetamide (DMA) in carbon tetrachloride in the range of 5~55$^{\circ}$C. The combination band in the three component system can be resolved into components due to monomeric TA, 1 : 1 TA-DMA complex and 1 : 2 TA-DMA complex. In the dilute solutions the experimental spectrum was resolved by using the computer into its two Lorentzian-Gaussian product components which have been identified with the monomeric TA and the 1 : 1 complex. The equilibrium constants and thermodynamic parameters of 1 : 1 complex were determined by analysis of concentration and temperature dependent spectra. The ${\Delta}H^{\circ}$ and ${\Delta}S^{\circ}$ for the 1 : 1 complex were -14.4 KJ mol$^{-1}$ and -15.6 J mol$^{-1}deg^{-1}$, respectively.

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An In-Band Noise Filtering 32-tap FIR-Embedded ΔΣ Digital Fractional-N PLL

  • Lee, Jong Mi;Jee, Dong-Woo;Kim, Byungsub;Park, Hong-June;Sim, Jae-Yoon
    • JSTS:Journal of Semiconductor Technology and Science
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    • v.15 no.3
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    • pp.342-348
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    • 2015
  • This paper presents a 1.9-GHz digital ${{\Delta}{\Sigma}}$ fractional-N PLL with a finite impulse response (FIR) filter embedded for noise suppression. The proposed digital implementation of FIR provides a simple method of increasing the number of taps without complicated calculation for gain matching. This work demonstrates 32 tap FIR filtering for the first time and successfully filtered the in-band phase noise generated from delta-sigma modulator (DSM). Design considerations are also addressed to find the optimum number of taps when the resolution of time-to-digital converter (TDC) is given. The PLL, fabricated in $0.11-{\mu}m$ CMOS, achieves a well-regulated in-band phase noise of less than -100 dBc/Hz for the entire range inside the bandwidth of 3 MHz. Compared with the conventional dual-modulus division, the proposed PLL shows an overall noise suppression of about 15dB both at in-band and out-of-band region.

Inestigation on the Structural Transition of n-type Ceramic Superconductor, $Nd_{2-x}Ce_xCuO_{4-\upsilon}$ System of CBED (수렴성전자회절에 의한 n-형 세라믹 초전도체 $Nd_{2-x}Ce_xCuO_{4-\upsilon}$의 결정구조 전이 연구)

  • 김정식;유광수
    • Journal of the Korean Ceramic Society
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    • v.34 no.2
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    • pp.139-144
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    • 1997
  • Structurally, the rare earth cuprate superconductor of Nd2-xCexCuO4-$\delta$ has T' structure and has been known as having a quite complicated microstructural phenomena, so far. In order to be superconductivity, both small amount of cation substitution of Nd3+ by Ce4+ and oxygen reduction are required. In the present study the crystallographic study on the structural transition for the Nd2-xCexCuO4-$\delta$ crystal has been con-ducted by observing the CBED (Convergent Beam Electron Diffraction) pattern with STEM(Scanning Transmission Electron Microscope). Three different samples of Nd2CuO3,Nd1.85Ce0.15CuO4 and Nd1.85Ce0.15CuO3.965 were prepared by solid-state sintering and their CBED patterns were observed by STEM to study the structural transition accompanying the substitution of Ce and the reduction of oxygen. Experimental HOLZ lines of these samples were compared with those plotted by a computer-programmed simulation to de-termine the lattice parameter of Nd2-xCexCuO4-$\delta$ crystal.

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광주천 인근 지하수의 수질 및 안정동위원소 특성

  • Yoon, Wook;Ji, Se-Jung
    • Proceedings of the KSEEG Conference
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    • 2003.04a
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    • pp.116-120
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    • 2003
  • 광주 지하수의 대수층은 주로 원형의 화강암 저지대 분지에 형성되어 있으며, 동남부 무등산(1,187m) 일대가 지하수의 주요 함양원 이다. 총 7,540 여 개의 지하수 관정으로부터 하루에 양수되는 추정 배출량은 59,455㎥ 이상으로 보고되고 있다(건설교통부,2000년). 도심지에서는 지하수가 생활 및 공업용수로 주로 이용되나, 농촌지역에서는 음용수 및 농업용수로 사용되고 있다. (중략)

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Production of ${\delta}-Aminolevulinic$ Acid in Soybean Curd Wastewater by Rhodobacter capsulatus KK-10 (두부공업폐수에서 Rhodobacter capsulatus KK-10을 이용한 ${\delta}-Aminolevulinic$ Acid의 생산)

  • Cheong, Dae-Yeol;Choi, Yang-Mun;Yang, Han-Chul;Cho, Hong-Yon
    • Applied Biological Chemistry
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    • v.40 no.6
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    • pp.556-560
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    • 1997
  • The removal efficiency of COD and the production of ${\delta}-aminolevulinic$ acid (ALA) were concurrently investigated for both purifying the soybean curd wastewater of high BOD and utilizing the wastewater as a renewable substrate of ALA production using Rhodobacter capsulatus KK-10. Its wastewater was a favorable media for the growth of photosynthetic bacteria in terms of its environmental characteristics having COD/BOD rate of 0.98, ratio of BOD : N : P=100 : 6 : 4, BOD/N ratio of 17.2, lactic acid of 1,080 ppm. Its COD value wastewater was decreased to 94% and dry cell weight was approached to about 1.2 g/l after cultivation of the photosynthetic bacteria for 4 days. By the addition of 15 mM levulinic acid (LA) into the wastewater at the middle log phase of cell growth, the amount of ALA secreted was 55 mg/l. The ALA production was considerably increased to 114 mg/l under the cultural condition of 15 mM supplementations of glycine and succinate with LA at the same period. Furthermore the maximum ALA production of 120 mg/l and COD removal efficiency of 92% were accomplished in the soybean curd wastewater enriched with one addition of 15 mM LA and three serial additions 15 mM ALA precursors.

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Planting Conditions of Korean Cannabis Derived from Stable Isotope Ratio & Tetrahydrocannabinol Contents (안정동위원소 비율 및 테트라하이드로칸나비놀 함량 분석을 통한 한국산 대마의 재배 환경 추론)

  • Lee, Jae-Sin;Park, Yong-Hoon;Rhee, Jong-Sook;Jeong, Jin-Il;Lim, Mi-Ae;Chung, Hee-Sun
    • YAKHAK HOEJI
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    • v.52 no.3
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    • pp.172-175
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    • 2008
  • Stable isotope ratio of carbon and nitrogen ($\delta^{13}C$ & $\delta^{15}N$), and $\Delta^{9}$-tetrahydrocannabinol (THC) contents were measured on 37 Korean cannabis and 10 commercial grade marijuana seized in Korea. Factors influencing on the measured values and their variations were investigated. $\delta^{13}C$ value of cannabis is specified mainly by water availability. Korean cannabis showed relatively low $\delta^{13}C$ values ranging -33.29$\sim$-27.01% (mean=-31.01%), which reflect geographic conditions of Korea where is rainy, especially during summer. $\delta^{15}N$ values, which reflect individual planting conditions, were relatively high up to -0.5$\sim$18.0% (mean=6.44%). It reflects characteristics of Korean cannabis growing wild in forest or cultivated in fertile soil. Tetrahydrocannabinol is the major hallucinogenic compound of cannabis. Ethanol extracts of cannabis leaves were derivatized by N,O-bis(trimethylsilyl)trifluoroacetamide (BSTFA), and the derivatives were analyzed by GC-MS in selected ion monitoring (SIM) mode. THC contents of Korean cannabis ranged 0.11$\sim$4.34% (mean=1.47%), which were relatively low compared with commercial grade marijuana.

Distribution of Fish Assemblage and Stable Isotope Composition of Reeds according to Geomorphic Characteristics of Lagoons along the East Sea (동해안 석호의 지형학적인 특성에 따른 어류군집분포와 갈대의 안정동위원소비)

  • Lee, Jaeyong;Park, Seungchul;Kim, Minseob;Choi, Jae-Seok;Lee, Kwangyeol;Shin, Kyunghoon
    • Korean Journal of Ecology and Environment
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    • v.48 no.1
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    • pp.1-11
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    • 2015
  • Abstract The purpose of study is to identify the relationship between stable isotope composition of reed stems in coastal and understand the structure of the fish community in 10 lagoons along the East Sea. The fish species composition (particularly, anadromous fish species) and relative abundance of trophic guilds was influenced by difference of geomorphic characteristics among lagoons. Reed stems ${\delta}^{13}C$ and ${\delta}^{15}N$ values ranged from $-28.40{\pm}0.11$‰ to $-26.87{\pm}0.25$‰ and $-1.09{\pm}1.45$‰ to $12.08{\pm}0.53$‰, respectively. The differences in reed stem ${\delta}^{15}N$ values might be associated with anthropogenic landuse and the geomorphic characteristics among lagoons. These results provide useful information to improve the conservation of fish habitats (biodiversity), preserve lagoon habitats and contribute to watershed management effect against anthropogenic pollution from watershed in these lagoon ecosystems.

MO Studies on the Electronic Structure and Reactivity of Glycinato, Glycine Ester Ligands (Glycinato 및 Glycine Ester 리간드의 전자구조와 반응성에 관한 분자궤도함수론적 연구)

  • Ja Hong Kim
    • Journal of the Korean Chemical Society
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    • v.24 no.1
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    • pp.15-19
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    • 1980
  • CNDO/2, EHT molecular orbital methods are used to investigate the electronic structure and reactivity of glycinato, glycine ester ligands. The results show that bidentate glycinato has a more stable structure, Gly-I with a $105.9^{\circ}$dihedral angle between ${\Delta}O_4C_3C_2$ and ${\Delta}C_3C_2N_1$ than Gly-Ⅱ. The electron inductive effects in the alkyl group substituted glycine ester ligands can also be derived from the calculation. According to the electron density, qN of ligands on the basis of CNDO/2 MO calculations, it is concluded that the stabilities are in the order of glycinato > Gly-Et-ester > Gly-i-Pr-ester > Gly-Me-ester.

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