• 농업과학연구
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• 제44권4호
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• pp.463-476
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• 2017

Climate change is considered as the greatest threat to our future and descendants. The Korean government has set a target for 2030 to reduce emission of greenhouse gases (GHGs) by 37% from the business-as-usual levels which are projected to reach 851 million metric tons of $CO_2eq$ (Carbon dioxide equivalent). In Korea, GHGs emission from agriculture account for almost 3.1% of the total of anthropogenic GHGs. The GHGs emitted from agricultural land are largely classified into three types: carbon dioxide ($CO_2$), methane ($CH_4$), and nitrous oxide ($N_2O$). In Korea, rice paddies are one of the largest agricultural $CH_4$ sources. In order to analyze domestic research trends related to $CH_4$ emission from rice paddies, 93 academic publications including peer reviewed journals, books, working papers, reports, etc., published from 1995 to September 2017, were critically reviewed. The results were classified according to the research purposes. $CH_4$ characteristics and assessment were found to account for approximately 65.9% of the research trends, development of $CH_4$ emission factors for 9.5%, $CH_4$ emission reduction technology for 14.8%, and $CH_4$ emission modeling for 6.3%, etc. A number of research related to $CH_4$ emission characteristics and assessment have been studied in recent years, whereas further study on $CH_4$ emission factors are required to determine an accurate country-specific GHG emission from rice paddies. Future research should be directed toward both studies for reducing the release of $CH_4$ from rice paddies to the atmosphere and the understanding of the major controlling factors affecting $CH_4$ emission.

• 대한화학회지
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• 제36권5호
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• pp.770-779
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• 1992

$Fe(CO)_5와 알킨일리튬의 반응에서 생성된 아실 음이온 착물을 CH_3CH_2OSO_2F로 처리하는 방법으로 5종의 철 알킨일카르벤 착물 유도체(1)들을 합성하였다. [R-C≡C-C(OCH_2CH_3)]Fe(CO)_4(R = n-프로필, 시클로헥실, t-부틸, 트리메틸실릴, 페닐). 트리메틸시릴기가 치환된 유도체(1d)와 8종의 열린 고리 1,3-디엔과의 반응에서 {\eta}^3-비닐카르벤 착물 유도체(2)를 주생성물로 얻었다.$

• Bulletin of the Korean Chemical Society
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• 제35권9호
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• pp.2615-2620
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• 2014

Ni/$La_2O_3$ with a high dispersion was prepared by reduction of $La_2O_3$ perovskite oxide to examine the catalytic activity for the $CO_2-CH_4$ reaction. The Ni/$La_2O_3$ catalyst was found to be highly active for the reaction. The ratios of $H_2$/CO were measured in a flow of the reaction mixture containing $CO_2/CH_4$/Ar using an on-line gas chromatography system operated at 1 atm and found to be varied with temperature between 0.66 and 1 in the temperature range of $500-800^{\circ}C$. A kinetic study of the catalytic reaction was performed in a static reactor at 40 Torr total pressure of $CO_2/CH_4/N_2$ by using a photoacoustic spectroscopy technique. The $CO_2$ photoacoustic signal varying with the concentration of $CO_2$ during the catalytic reaction was recorded as a function of time. Rates of $CO_2$ disappearance in the temperature range of $550-700^{\circ}C$ were obtained from the changes in the $CO_2$ photoacoustic signal at early reaction stage. The plot of ln rate vs. 1/T showed linear lines below and above $610^{\circ}C$. Apparent activation energies were determined to be 10.4 kcal/mol in the temperature range of $550-610^{\circ}C$ and 14.6 kcal/mol in the temperature range of $610-700^{\circ}C$. From the initial rates measured at $640^{\circ}C$ under various partial pressures of $CO_2$ and $CH_4$, the reaction orders were determined to be 0.43 with respect to $CO_2$ and 0.33 with respect to $CH_4$. The kinetic results were compared with those reported previously and used to infer a reaction mechanism for the Ni/$La_2O_3$-catalyzed $CO_2-CH_4$ reaction.

• 청정기술
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• 제17권4호
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• pp.389-394
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• 2011

바이오가스로부터 이산화탄소와 질소를 제거하기 위한 흡착공정은 많이 논의되고 있다. 특히 흡착공정 중에서 압력변동흡착(Pressure swing adsorption)공정은 에너지소모가 적고 가격이 경제적이기 때문에 기체의 분리와 정제를 위한 공정으로 적절하다. 물리적 흡착을 사용하는 PSA공정은 흡착과 탈착이 가능하다. 각 cycle단계의 구성은 가압, 주입 및 흡착, 압력 균등화, 감압 및 세정으로 이루어져있다. 본 실험에서 PSA공정은 이산화탄소와 질소를 제거하기 위한 흡착제로 zeolite 13X와 carbon molecular sieve (CMS)로 구성되어 있으며, 혼합 가스의 농도는 $CH_4/CO_2/N_2$ (75:21:4 vol%)의 비율을 갖고 있다. 각각 zeolite 13X와 CMS는 선택적으로 혼합가스로부터 질소와 이산화탄소를 흡착하여 분리하고 제거한다. 또한 CMS의 경우는 빠르게 분산되는 이산화탄소의 처리량이 높다. 상부탱크, 하부탱크, 주입탱크의 가스 조성은 TCD 검출기를 이용하는 gas chromatography (GC)에 의해서 측정되었다.

• 대한화학회지
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• 제62권5호
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• pp.344-351
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• 2018

이 연구에서는 기체 상태 페난트렌, 페난트렌올, 페난트레닐 라디칼, 하이드록실 페난트렌 라디칼에 대한 IR 스펙트럼을 BLYP/6-311++G(d,p)법을 사용하여 얻었다. 이 스펙트럼들을 비교함으로써 ${\cdot}OH$에 의한 페난트렌의 분해 반응 경로를 동정하는데 IR 스펙트럼 측정이 유용하게 사용될 수 있음을 볼 수 있었다. IR 스펙트럼에서 H 원자 제거 과정은 CH의 out-of-plane 굽힘 진동 영역인 $650{\sim}850cm^{-1}$, ${\cdot}OH$ 첨가 과정은 CH 신축 및 굽힘 진동 영역에서 용이하게 확인 할 수 있음을 알 수 있었다. 또한 5종의 페난트렌-n-올 (n = 1, 2, 3, 4, 9) 모두에 대하여 얻어진 IR 스펙트럼 역시 여기에 주어졌다.

• 유기물자원화
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• 제14권2호
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• pp.63-70
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• 2006

본 연구에서는 폐기물매립지의 안정화 정도를 용이하게 평가하기 위하여 매립폐기물의 분해정도를 수치화 할 수 있는 매립지의 안정화 지수 개발을 목적으로 하였다. 안정화 지수를 개발하기 위하여 50개소의 사용종료 매립지를 대상으로 침출수 수질, 매립가스 조성, 매립폐기물의 물리화학적 특성 자료를 수집하여 이들의 매립연령별 환경특성을 고찰하였다. 그리고 이들 환경지표중 폐기물매립지의 안정화와 상관도가 높은세부 환경지표로서 침출수의 BOD/CODcr, 발생가스중의 $CH_4$농도, 매립폐기물의 C/N가 안정화 지표로 선정하였다. 각 지표에 대한 매립연령별 추세선을 이용하여 지수화한 결과 매립지 안정화 지수로 다음과 같은 식을 얻을 수 있었다. $$I_{LS}=S_L+S_G+S_W$$ $$S_L=-\{4.892+16.587{\cdot}ln[BOD/COD_{Cr]\}$$ $$S_G=53.872-12.782{\cdot}ln[CH_4]$$ $$S_W=79.382-20.013{\cdot}ln[C/N]$$ (단, $S_L$, $S_G$, and $S_W$는 각각 33.3점이 최대값이다.) 여기서, $I_{LS}$ : 매립지 안정화 지수 $S_L$ : 침출수의 안정화 점수 $S_G$ : 매립가스의 안정화 점수 $S_W$ : 폐기물의 안정화 점수.

• Restorative Dentistry and Endodontics
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• 제44권1호
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• pp.10.1-10.11
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• 2019

Objectives: The objective of this study was to assess coronal discoloration induced by the following intracanal medicaments: calcium hydroxide (CH), a mixture of CH paste and chlorhexidine gel (CH/CHX), and triple antibiotic paste (3Mix). Materials and Methods: Seventy extracted single-canal teeth were selected. Access cavities were prepared and each canal was instrumented with a rotary ProTaper system. The specimens were randomly assigned to CH, CH/CHX, and 3Mix paste experimental groups (n = 20 each) or a control group (n = 10). Each experimental group was randomly divided into 2 subgroups (A and B). In subgroup A, medicaments were only applied to the root canals, while in subgroup B, the root canals were completely filled with medicaments and a cotton pellet dipped in medicament was also placed in the pulp chamber. Spectrophotometric readings were obtained from the mid-buccal surface of the tooth crowns immediately after placing the medicaments (T1) and at 1 week (T2), 1 month (T3), and 3 months (T4) after filling. The ${\Delta}E$ was then calculated. Data were analyzed using 2-way analysis of variance (ANOVA), 3-way ANOVA, and the $Scheff{\acute{e}}$ post hoc test. Results: The greatest color change (${\Delta}E$) was observed at 3 months (p < 0.0001) and in 3Mix subgroup B (p = 0.0057). No significant color change occurred in the CH (p = 0.7865) or CH/CHX (p = 0.1367) groups over time, but the 3Mix group showed a significant ${\Delta}E$ (p = 0.0164). Conclusion: Intracanal medicaments may induce tooth discoloration. Use of 3Mix must be short and it must be carefully applied only to the root canals; the access cavity should be thoroughly cleaned afterwards.

• 한국대기환경학회:학술대회논문집
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• 한국대기환경학회 1999년도 추계학술대회 논문집
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• pp.277-279
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• 1999

대기 중으로 배출되는 $CO_2$, CH$_4$, $N_2$O, $O_3$, CFC 등은 지구온난화에 기여하고, 이러한 온실기체들은 여러 경로를 통해서 대기로 배출되고 있다. 배출원별 온실기체의 기여도를 보면(Green peace, 1997) 화석연료 연소의 경우가 58%로 가장 높고, 농업과 토지이용의 변화에 의해 18%, 17%, 그리고 도시쓰레기의 매립에 의해서도 약 3%정도 기여하는 것으로 보고되었다. 주요 온실기체에 대한 대기 중 농도가 과거보다 현저하게 증가되었음이 확인되고 있고, $CO_2$의 경우 년간 증가율이 0.5%, CH$_4$의 경우는 1%, 그리고 $N_2$O의 경우는 약 0.2% 정도로 보고되고 있다.(Bouwman, 1990).(중략)

• 한국진공학회:학술대회논문집
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• 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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• pp.119-119
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• 2011

This study examined the synthesis of large area graphene and the change of its characteristics depending on the ratio of CH4/H2 by using the thermal CVD methods and performed the experiments to control the electron-hole conduction and Dirac-point of graphene by using chemical doping methods. Firstly, with regard to the characteristics of the large area graphene depending on the ratio of CH4/H2, hydrophobic characteristics of the graphene changed to hydrophilic characteristics as the ratio of CH4/H2 reduces. The angle of contact also increased to 78$^{\circ}$ from 58$^{\circ}$. According to the results of Raman spectroscopy showing the degree of defect, the ratio of I(D)/I(G) increases to 0.42% from 0.25% and the surface resistance also increased to 950 ${\Omega}$ from 750 ${\Omega}$/sq. As for the graphene synthesis at the high temperature of 1,000$^{\circ}$ by using CH4/H2 in a Cu-Foil, the possibility of graphene formation was determined as a function of the ratio of H2 included in the fixed quantity of CH4 as per specifications of every equipment. It was observed that the excessive amount of H2 prevented graphene from forming, as extra H-atoms and molecules activated the reaction to C-bond of graphene. Secondly, in the experiment for the electron-hole conduction and the Dirac-point of graphene using the chemical doping method, the shift of Dirac-point and the change in the electron-hole conduction were observed for both the N-type (PEI) and the P-type (Diazonium) dopings. The ID-VG results show that, for the N-type (PEI) doped graphene, Dirac-point shifted to the left (-voltage direction) by 90V at an hour and by 130 V at 2 hours respectively, compared to the pristine graphene. Carrier mobility was also reduced by 1,600 cm2/Vs (1 hour) and 1,100 cm2/Vs (2 hours), compared to the maximum hole mobility of the pristine graphene.

• 대한화학회지
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• 제36권2호
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• pp.318-323
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• 1992

Vinylsulfilimine 유도체(H, p-$CH_3$, m-TEX>$CH_3$, p-Cl, p-Br, p-$OCH_3$, 및 p-$NO_2$)에 1-methyl-5-mercapto-1,2,3,4-tetrazole을 반응시켜 다음 7가지의 새로운 호합물을 합성하였다. S-Phenyl-S-2-(1-methyl-1,2,3,4-tetrazole-5-thio)-ethyl-N-p-tosylsulfilimine, S-p-tolyl-S-2-(1-methyl-1,2,3,4-tetrazole-5-thio)-ethyl-N-p-tosylsulfilimine, S-m-tolyl-S-2-(1-methyl-1,2,3,4-tetrazole-5-thio)-ethyl-N-p-tosylsulfilimine, S-p-chlorophenyl-S-2-(1-methyl-1,2,3,4-tetrazole-5-thio)-ethyl-N-p-tosylsulfilimine, S-p-bromophenyl-S-2-(1-methyl-1,2,3,4-tetrazole-5-thio)-ethyl-N-p-tosylsulfilimine, S-p-methoxyphenyl-S-2-(1-methyl-1,2,3,4-tetrazole-5-thio)-ethyl-N-p-tosylsulfilimine and S-p-nitrophenyl-S-2-(1-methyl-1,2,3,4-tetrazole-5-thio)-ethyl-N-p-tosylsulfilimine. 이 화합물들의 구조는 원소분석, MP, UV, IR 및 NMR 스펙트럼에 의해 확인되었다.