• 제목/요약/키워드: $CH_{4}$

검색결과 3,760건 처리시간 0.028초

Estimation of CH4 oxidation efficiency in an interim landfill cover soil using CO2/CH4 ratios

  • Park, Jin-Kyu;Lee, Won-Jae;Ban, Jong-Ki;Kim, Eun-Cheol;Lee, Nam-Hoon
    • Environmental Engineering Research
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    • 제20권2호
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    • pp.191-197
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    • 2015
  • The first objective of this study was to discuss the applicability of the $CO_2/CH_4$ ratio method in order to assess $CH_4$ oxidation efficiency. To achieve this objective, a comparison between $CO_2/CH_4$ ratios and the mass balance method was conducted. The second objective of this study was to estimate the $CH_4$ oxidation efficiency in an interim landfill soil cover and assess how a $CH_4$ influx influences the $CH_4$ oxidation efficiency. The results showed that despite the $CO_2$ problems brought by respiration, the $CH_4$ oxidation efficiencies obtained by the $CO_2/CH_4$ ratio method led to similar results compared to the mass balance method. In this respect, the $CO_2/CH_4$ ratio method can be an indicator of the $CH_4$ oxidation efficiencies for landfill cover soils. The $CH_4$ oxidation efficiencies derived in this study through the $CO_2/CH_4$ ratio method ranged between 46% and 64%, and between 41% and 62% through the mass balance method. The results imply that the Intergovernmental Panel on Climate Change's (IPCC) default value of 10% for the $CH_4$ oxidation efficiency is an underestimation for landfill cover soils. $CH_4$ oxidation efficiency tends to be negatively correlated with $CH_4$ influx. Therefore, $CH_4$ influx reaching a landfill cover should be limited in order to increase the $CH_4$ oxidation efficiency.

부틸아미드옥심 유도체의 몰리브덴(Ⅵ) 사핵 착물의 합성과 성질 (Synthesis and Characterization of Tetranuclear Molybdenum(Ⅵ) Complexes with Butylamidoxime Derivatives)

  • 로수균;오상오
    • 대한화학회지
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    • 제39권7호
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    • pp.552-558
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    • 1995
  • 배위자인 이소부틸, 노르말 부틸 및 메틸티오아세트아미드옥심과 출발 물질인 단핵 및 다핵 착물과의 반응에서 $X_2[M_{O4}O_12{R'C(NH_2)NO}_2](X=n-Bu_4N^+$, $R'=(CH_3)_2CH$, $CH_3CH_2CH_2$, $CH_3SCH_2$; $X=(CH_3)_2CHC(=NH_2)NH_2^+$, $R'=(CH_3)_2CH$; $X=CH_3CH_2CH_2C(=NH_2)NH_2^+$, $R'=CH_3_CH_2CH_2$; $X=CH_3SCH_2C(=NH_2)NH_2^+$, $R'=CH_3SCH_2)$을 합성하였다. 합성한 착물은 원소분석, 적외선 및 핵자기공명에 의해 구조를 규명하였다. 얻은 착물중 ${(CH_3)_2CHC(NH_2)_2}_2[M_{O4}O_{12}{(CH_3)_2CHC(NH_2)NO}_2]$은 X-선 단결정 회절에서 결정구조를 밝혔고, 얻은 데이타는 Monoclinic, $P2_{1/c}$, $a=10.168(3){\AA}$, $b=11.768(1){\AA}$, $c=13.557(1){\AA}$, ${\beta}=102.08(1)^{\circ}$, $V=1586.2(5){\AA}^3$, Z = 2이었고, 회절강도 2951개($F_0>3s(F_0)$)에 대한 최종 신뢰도 인자는 0.026이었다. 이 착물의 구조는 평면상의 환형$[Mo_4({\mu}-O)_4]$과 두 개의 ${\mu}_4$-아미드옥시메이트로 구성되어 있다.

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Iridium(Ⅲ) Complexes of η$^6$-Arenes with Olefinic and Cyclopropyl Substituents: Facile Conversion to η ³-henylallyl Complexes

  • 정현목;주광석;진종식
    • Bulletin of the Korean Chemical Society
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    • 제18권4호
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    • pp.402-405
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    • 1997
  • Olefinic and cyclopropyl group substituted arenes (C6H5Y) react with [Cp*Ir(CH3COCH3)3]A2 (A=ClO4-, OTf-) to give η6-arene complexes, [Cp*Ir(η6-C6H5Y)]2+ (1a: Y=-CH=CH2 (a),-CH=CHCH3 (b),-C(CH3)=CH2 (c),-CH-CH2-CH2 (d)). Complex 1b-1d are readily converted into η3-allyl complexes, [Cp*(CH3CN)Ir(η3-CH(C6H5)CHCH2)]+ (2a) and [Cp*(CH3CN)Ir(η3-CH2(C6H5)CH2)]+ (2b), in the presence of Na2CO3 in CH3CN. The η6-styrene complex, 1a reacts with NaBH4 to give η5-cyclohexadienyl complex, [Cp*Ir(η5-C6H6-CH=CH2)]+ (3), while with H2 it gives η6-ethylbenzene complex [Cp*Ir(η6-C6H5CH2CH3)]2+ (4). Complex 1a and 1c react with HCl to give [Cp*Ir(η6-C6H5CH2CH2Cl)]2+ (5a) and [Cp*Ir(η6-C6H5CH(CH3)CH2Cl]2+ (5b), respectively.

Synthesis and Characterization of Various Di-N-Functionalized Tetraaza Macrocyclic Copper(II) Complexes

  • Kang, Shin-Geol;Kim, Na-Hee;Lee, Rae-Eun;Jeong, Jong-Hwa
    • Bulletin of the Korean Chemical Society
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    • 제28권10호
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    • pp.1781-1786
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    • 2007
  • Two copper(II) complexes, [CuL3](ClO4)2 bearing one N-CH2CH2CONH2 group as well as one N-CH2CH2CN group and [CuL4](ClO4)2 bearing two N-CH2CH2CONH2 groups, have been prepared by the selective hydrolysis of [CuL2](ClO4)2 (L2 = C-meso-1,8-bis(cyanoethyl)-5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane). The complex [CuL5](ClO4)2 bearing one N-CH2CH2C(=NH)OCH3 and one N-CH2CH2CN groups has been prepared as the major product from the reaction of [CuL2](ClO4)2 with methanol in the presence of triethylamine. In acidic aqueous solution, the N-CH2CH2C(=NH)OCH3 group of [CuL5](ClO4)2 undergoes hydrolysis to yield [CuL6](ClO4)2 bearing both N-CH2CH2COOCH3 and N-CH2CH2CN groups. The crystal structure of [CuL5](ClO4)2 shows that the complex has a slightly distorted square-pyramidal coordination polyhedron with an apical Cu-N (N-CH2CH2C(=NH)OCH3 group) bond. The apical Cu-N bond distance (2.269(3) A) is ca. 0.06 A longer than the apical Cu-O (N-CH2CH2CONH2 group) bond of [CuL4](ClO4)2. The pendant amide group of [CuL3](ClO4)2 is involved in coordination. The carboxylic ester group of [CuL6](ClO4)2 is also coordinated to the metal ion in various solvents but is removed from the coordination sphere in the solid state.

Reactions, Hydrogenation and Isomerization of Unsaturated Esters with a Rhodium(I)-Perchlorato Complex

  • Jeong Hyun Mok;Chin Chong Shik
    • Bulletin of the Korean Chemical Society
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    • 제7권6호
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    • pp.468-471
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    • 1986
  • The isolated products from the reactions of $Rh(ClO_4)(CO)(PPh_3)_2$ (1) with CH_2$ = $CHCO_2C_2H_5$ (2) and trans-$CH_3CH$ = $CHCO_2C_2H_5$ (3) contain 80∼ 90% of $[Rh(CH_2 = CHCO_2C_2H_5)(CO)(PPh_3)_2]ClO_4$ (4) and [Rh(trans-$CH_3CH = CHCO_2C_2H_5(CO)(PPh_3)_2]ClO_4$ (5), respectively where 2 and 3 seem to be coordinated through the carbonyl oxygen. It has been found that complex 1 catalyzes the isomerization of $CH_2 = CH(CH_2)_8CO_2C_2H_5$ (6) to $CH_3(CH_2)_nCH = CH(CH_2)_{7-n}CO_2C_2H_5$ (n = 0∼7) under nitrogen at 25$^{\circ}C$. The isomerization of 6 is slower than that of $CH_2 = CH(CH_2)_9CH_3$ to $CH_3(CH_2)_nCH$ = $CH(CH_2)_{8-n}CH_3$ (n = 0∼8), which is understood in terms of the interactions between the carbonyl oxygen of 6 and the catalyst. It has been also observed that complex 1 catalyzes the hydrogenation of 2, 3, 6, trans-$C_6H_5CH = CHCO_2C_2H_5$ (7), $CH_3(CH_2)_7CH = CH(CH_2)_7CO_2C_2H_5$ (8) and $CH_2 = CH(CH_2)_9CH_3$ (9), and the isomerization (double bond migration) of 6 and 9 under hydrogen at 25$^{\circ}C$. The interactions between the carbonyl oxygen of the unsaturated esters and the catalyst affect the hydrogenation in such a way that the hydrogenation of the unsaturated esters becomes slower than that of simple olefins.

WRF-CMAQ 모델을 이용한 한반도 CH4 배출의 기여농도 추정 및 검증 (Verification and Estimation of the Contributed Concentration of CH4 Emissions Using the WRF-CMAQ Model in Korea)

  • 문윤섭;임윤규;홍성욱;장은미
    • 한국지구과학회지
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    • 제34권3호
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    • pp.209-223
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    • 2013
  • 이 연구의 목적은 한반도에서 $CH_4$ 농도의 수치모의 검증을 통하여 $CH_4$ 배출원의 기여 농도를 추정하는 것이고, 이 수치모의에 사용된 $CH_4$ 배출량을 상자모델로부터 추정된 $CH_4$ 배출량과 비교하는 것이다. 한반도에서 2010년 4월 1일부터 8월 22일까지 $CH_4$의 평균 농도를 추정하기 위해 WRF-CMAQ 모델이 사용되었다. 모델에서 $CH_4$ 배출량은 전지구 배출량인 EDGAR와 한국에서의 온실기체 배출량인 GHG-CAPSS로부터 인위적 배출 인벤토리와 전지구 자연적 인벤토리인 MEGAN이 적용되었다. 이들 $CH_4$ 배출량은 안면도 및 울릉도에서 측정된 $CH_4$ 농도와 모델링 농도 자료를 비교함으로써 검증되었다. 울릉도에서 국내 배출원으로부터 추정된 $CH_4$의 기여 농도는 약 20%로 나타났고, 이것은 한반도 내 농장(8%), 에너지 기여 및 산업공정(6%), 일반폐기물(5%), 생체 및 토지이용(1%) 등 $CH_4$ 배출원으로부터 기원하였다. 그리고 중국으로부터 수송된 $CH_4$의 기여 농도는 약 9%였고, 나머지 배경농도는 약 70%로 나타났다. 박스모델로 추정된 $CH_4$ 배출량은 WRF-CMAQ 모델에서 사용한 $CH_4$ 배출량과 유의미한 결과를 얻었다.

A Comparison of the Leaving Group Ability of Transition Metal Carbonyl Anions vs. Halides : Reaction of $MH^-$ with M'-R $(MH^-\;=\;HW(CO)_4\;-P(OMe)_3\;^-,\;HW(CO)_5\;^-,\;HCr(CO)_5\;^-,\;HFe(CO)_4\;^-;\;M'-R=CpMo(CO)_3(CH_3),\;CpMo(CO)_3{CH_2CH(CH_2)_2})$

  • Yong Kwang Park;Seon Joong Kim;Carlton Ash
    • Bulletin of the Korean Chemical Society
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    • 제11권2호
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    • pp.109-114
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    • 1990
  • The anionic transition metal hydrides $(HW(CO)_4P(OMe)_3\;^-,\;HW(CO)_5\;^-,\;HCr(CO)_5\;^-,\;HFe(CO)_4\;^-)$ react with transition metal alkyl $(CpMo(CO)_3(CH_3)$ to yield $CH_4\;and\;CH_3CHO$ in addition to the inorganic products $(CpMo(Co)_3\;^-$, etc.). The reaction of these anionic metal hydrides with CpMo(CO)3{CH2CH(CH2)2} may lead to an elucidation of the reaction mechanisms involved; the organic product distributions are among $CH_4,\;CH_2\;=\;CHCH_2CH_3$, and $CH_3CH(CH_2)_2$, depending upon the anionic metal hydride used. These anionic metal hydrides also are reported to undergo a hydride-halide exchange reaction with organic halides; therefore, these similar reactions have been compared in terms of leaving group ability $(CpMo(CO)_3\;^-\;vs.\;Br^-)$ and the mechanistic pathways.

마이크로파 플라즈마의 광방출 스펙트럼 (optical emission spectra of microwave plasma)

  • 박상현;구효근;심정봉;김경환;박재윤;이덕출
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 1998년도 추계학술대회 논문집 학회본부 C
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    • pp.895-897
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    • 1998
  • The optical spectra of microwave plasma by four kinds of gases($N_2$, $N_2-CH_4$, $H_{2}-CH_{4}$ and Air-$CH_4$) have been measured for investigating 388.4[nm] peak which has the same intensity as $H_{\alpha}$(656.4[nm]) peak. A 388.4[nm] peak by $N_2$ plasma, $N_{2}-CH_{4}$ plasma and Air-$CH_4$ plasma may be CN peak because it is with 337.1, 357.8 and 316.0[nm] peaks by $N_2$. And a 388.4[nm] peak by $H_{2}-CH_{4}$ plasma without by $N_2$ 337.1, 357.8 and 316.0[nm] peaks may be CH peak. In the investigation results for optical spectra by $H_{2}-CH_{4}$ plasma and $H_{2}-CH_{4}-O_{2}$ plasma, the density of hydrogen atom was increased because oxygen decompose hydrogen molecules in $H_{2}-CH_{4}$ plasma with oxygen. These hydrogen atom decompose $CH_4$ and increase CH radical. And the crystalline of deposited diamond was good and the growth rate increased.

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SnO2:Cu 나노 구조물의 CH4, CH3CH2CH3 가스 감응 특성 (Gas Sensing Behaviors of SnO2:Cu Nanostructures for CH4, CH3CH2CH3 Gas)

  • 이지영;유윤식;유일
    • 한국전기전자재료학회논문지
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    • 제25권12호
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    • pp.974-978
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    • 2012
  • The effect of Cu coating on the sensing properties of nano $SnO_2:Cu$ based sensors for the $CH_4$, $CH_3CH_2CH_3$ gas was studied. This work was focussed on investigating the change of sensitivity of nano $SnO_2:Cu$ based sensors for $CH_4$, $CH_3CH_2CH_3$ gas by Cu coating. Nano sized $SnO_2$ powders were prepared by solution reduction method using stannous chloride($SnCl_2{\cdot}2H_2O$), hydrazine($N_2H_2$) and NaOH and subsequent heat treatment. XRD patterns showed that nano $SnO_2$ powders with rutile structure were grown with (110), (101), (211) dominant peak. The particle size of nano $SnO_2:Cu$ powders at 8 wt% Cu was about 50 nm. $SnO_2$ particles were found to contain many pores, according to SEM analysis. The sensitivity of nano $SnO_2:Cu$ based sensors was measured for 5 ppm $CH_4$ gas and $CH_3CH_2CH_3$ gas at room temperature by comparing the resistance in air with that in target gases. The sensitivity for both $CH_4$ and $CH_3CH_2CH_3$ gases was improved by Cu coating on the nano $SnO_2$ surface. The response time and recovery time of the $SnO_2:Cu$ gas sensors for the $CH_4$ and $CH_3CH_2CH_3$ gases were 18~20 seconds, and 13~15 seconds, respectively.

고리형 아민이 포함된 메탄 하이드레이트의 튜닝과 가스 저장 연구 (Tuning Behavior of (Cyclic Amines + Methane) Clathrate Hydrates and Their Application to Gas Storage)

  • 박기훈;김동현;차민준
    • Korean Chemical Engineering Research
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    • 제61권3호
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    • pp.394-400
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    • 2023
  • 이 연구에서는 메탄 가스(CH4)와 함께 사이클로프로필아민(cyclopropylamine, CPrA)과 사이클로펜틸아민(cyclopentylamine, CPeA)을 이용한 하이드레이트의 튜닝효과, 가스 저장량, 그리고 하이드레이트의 열팽창 거동에 대해 논의하였다. 메탄 가스의 저장량을 극대화시킬 수 있도록 하이드레이트 튜닝 효과를 하이드레이트에 투입된 객체 분자의 농도를 달리 함에 따라 알아보았다. (CPrA+CH4) 하이드레이트의 경우, 0.5 mol% 정도의 농도에서 최대 튜닝효과가 발생하였으며, (CPeA+CH4) 하이드레이트는 기존 연구와 유사한 1.0 mol% 정도의 농도에서 최대 튜닝 효과가 발생하였다. (CPrA + CH4), (CPeA + CH4) 하이드레이트 모두 구조 II 하이드레이트를 형성한다고 알려진(테트라하이드로퓨란 + CH4), (사이클로펜탄 + CH4) 하이드레이트보다 더 많은 가스량을 저장하는 것으로 밝혀졌다. 100, 150, 200, 250 K의 조건에서(CPrA + CH4), (CPeA + CH4) 하이드레이트의 분말 X-선 회절 분석을 통해 각 온도별 격자 크기를 알아내고 그 차이를 분석하여 열팽창 거동을 분석하였다. 이에 따라, 객체 분자의 크기 차이로 인해(CPeA + CH4) 하이드레이트의 격자 상수가 더 큰 것으로 확인되었다.