• Title/Summary/Keyword: 2N 이중화

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고분자(高分子) 재료(材料)의 오존열화(劣化) 및 방지(防止) 메커니즘

  • Heo, Dong-Seop
    • Elastomers and Composites
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    • v.16 no.4
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    • pp.217-227
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    • 1981
  • 오존은 PE나 고무 등 고분자재료(高分子材料)의 표면(表面)에 존재하는 이중결합(二重結合)에 대(對)하여 친전자적부가반응(親電子的付加反應)으로 ozonide가 생성되고 이어서 제(第)3급(級) 수소(水素)를 공격하므로서 주쇄(主鎖)가 절단된다. 따라서 aldehyde, ketone 등의 carbonyl 화합물(化合物)이 생성된다. 이들이 재료표면(材料表面)의 굴곡변형(變形)의 증가에 따라 열(熱) 또는 공(光)에 의하여 다시 분해(分解)를 촉진시킨다. 2개(個)의 N분자(原子)에 방향족(芳香族) 및 지방족기(脂肪族基)를 각각 치환시킨 p - phenylene diamine 유도체(誘導體) 등과 같은 전자공흥성(電子供與性)이 큰 화합물(化合物)은 친전자적(親電子的)인 오존과 우선적으로 3급(級) 수소에 비하면 약 100 배(倍)로 반응성이 크다는것을 표(表)3으로 알수 있다. 미단이중결합(未端二重結合)에 대한 오존과의 반응은 다음 반응식과 같이 이중결합(二重結合)에 오존의 부가반응(付加反?)으로 개시(開始)되어 peroxi methylene이 유리되면서 미단(未端)은 aldehyde로 변화한다. 또 1개의 반응은 제(第)3급(級) 탄소-수소 결합에 오존이 삽입되고 계속 일어나는 분해반응으로서 hydroperoxide의 생성 및 탈염화수소(脫鹽化水素)반응이 일어난다. 이와같은 반응(反?)으로 생성(生成)된 내부(內部) 이중결합(二重結合)에 대한 오존의 반응은 olefin의 경우와 마찬가지로 molozonide나 ozonide의 과정을 거쳐 주쇄(主鎖)가 개열(開裂)되는 것이다.

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Stress analysis of the CR lens using the chrome conversion (Chrome 변환을 이용한 CR 렌즈의 미세응력 시각화)

  • Kim, Yong-Geun
    • Journal of Korean Ophthalmic Optics Society
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    • v.10 no.1
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    • pp.9-15
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    • 2005
  • The polariscope to measure the microscopic stress in CR lens consists of light source polarizer, model, polarizer, CCD, computer, chrome conversion orderly and the principal-stressed difference, (${\sigma}_1-{\sigma}_2$) and the fringe order n were measured by analyzing two components of light wave $E_1$ and $E_2$ following each polarizer's steps. The two-dimensional model could be determined from the fact that the optical axes of sample concide with the principal-stress directions. The bi-refringence acted to a light wave and the phase retardation were in proportion to the principal-stressed difference(${\sigma}_1-{\sigma}_2$) and the intensity of final light wave was proportioned to $sin2({\Delta}/2)$ and when ${\Delta}/2=n{\pi}$ (n=0, 1, 2, ${\ldots}$) the extinction occurs. Photoelastic's image by microscopic stress could analyzed using chrome conversion, and the image showed clearly.

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The effect of hydrogen dilution ratio on the crystallization of hydrogenated amorphous silicon thin films (수소화된 비정질 실리콘 박막의 결정화에 수소의 희석비가 미치는 영향)

  • 이유진;신진국
    • Proceedings of the Materials Research Society of Korea Conference
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    • 2003.03a
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    • pp.98-98
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    • 2003
  • 비정질 실리콘 박막을 태양전지, 박막 트랜지스터, 이미지 센서, 컬러 디텍터 등에 적용하기 위한 많은 연구가 진행되고 있다. 이중 태양전지에 적용하기 위한 비정질 실리콘 박막은 p/i/n 다이오드 구조를 형성하게 되는데, 태양전지의 효율을 증가시키기 위해 결정질을 형성하거나 실리콘 화합물 박막을 적용한다. 본 연구에서는 비정질 태양전지의 흡수층(absorption layer)으로 사용되는 수소화된 비정질 박막의 결정화에 수소의 희석비가 미치는 영향을 파악하고자 하였다. PECVD 장비로 실란(SiH$_4$)과 수소(H$_2$) 가스를 이용하여 실리콘 박막을 증착하였고, 수소의 희석비(dilution ratio)를 변화시켜 비정질 실리콘 박막 내에 결정질 실리콘이 형성되는 정도를 관찰하였다. SEM과 Raman Spectroscopy를 이용해 박막의 두께 및 결정화도를 측정하였다. 실란에 대한 수소의 희석비가 증가할수록 증착률은 낮아지지만, 결정화도가 높아지는 것을 관찰할 수 있었다. 본 연구에서 형성한 결정질 실리콘 박막을 태양전지의 흡수층에 적용하면 효율 증가에 크게 기여할 것으로 판단된다.

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Decentralized Composting of Garbage by a Small Composter for a Dwelling House;V. Field experiment (가정용 소형 퇴비화용기에 의한 부엌쓰레기의 분산식 퇴비화;V. 현장조건에서 퇴비화)

  • Seo, Jeoung-Yoon;Joo, Woo-Hong
    • Korean Journal of Environmental Agriculture
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    • v.15 no.2
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    • pp.179-187
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    • 1996
  • This study was conducted to investigate the possibility of composting of household garbage. The composter with the double layer walls was operated for 60 days in each season. The following results were obtained at the end of the experiment, if the time was not specified. 1) The maximum temperature was $31^{\circ}C$ in spring, $36^{\circ}C$ in summer and $50^{\circ}C$ in winter. 2) The mass was reduced to an average of 58.5%. 3) pH values of the compost were 8.21 in spring, 8.29 in summer and 7.94 in winter. 4) The ash contents were 55.8% in spring, 57% in summer and 73.8% in winter. 5) The nitrogen contents were in the range of $0.2{\sim}5.8%$. Its values were the highest in winter and the lowest in summer. 6) Inorganic contents of the compost were in the range of : $P_2O_5$ ; $1.5{\sim}4.41%$, $K_2O$ ; $0.02{\sim}1.31%$, CaO $0.13{\sim}1.68%$ and MgO $0.05{\sim}1.22%$. 7) Heavy metal contents of the compost were in the range of : Zn ; $13{\sim}89mg/kg$, Cu ; $4{\sim}62mg/kg$, Cd ; $1{\sim}21mg/kg$, Pb ; $N.D.{\sim}97mg/kg$, Cr ; $N.D.{\sim}37$ and Hg ; $N.D.{\sim}1.38mg/kg$.

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Studies on the Synthesis of 1-Hydroxycarbapenems (1-히드록시카르바페넴의 합성에 관한 연구)

  • You, Jong Hyeon;Park, Jeong Ho;Goo, Yang Mo;Lee, Yun Yeong
    • Journal of the Korean Chemical Society
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    • v.42 no.1
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    • pp.69-77
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    • 1998
  • (3S,4S)-1-(t-Butoxycarbonylmethyl)-3-[(S)-1-(t-butyldimethylsilyloxy)ethyl]-4-(2-diazo-2-ethoxycarbonyl-1-oxoethyl)-2-azetidinone (14) was prepared from 4-styryl-2-azetidinone 7b via a sequence of reactions involving N-alkylation with bromoacetate, ozonolysis, oxidation, condensation with magnesium ethyl malonate, and diazo transfer reaction. (3S,4S)-3-[(S)-1-(t-Butyldimethylsilyloxy)ethyl]-4-(3-diazo-3-ethoxycarbonyl1-hydroxypropyl)-2-azetidinone (21) was also prepared from 4-formyl-2-azetidinone 5b via a sequence of reactions involving Wittig reaction, 1,3-dipolar cycloaddition with ethoxycarbonylformonitrile oxide, catalytic hydrogenation, and diazotization. However, the final cyclization of 14 or 21 to 1-hydroxycarbapenem or 1-hydroxycarbapenam by treating with $Rh_2(OAc)_4$ was unsuccessful.

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Gas-chromatographic determination of methylthiohydantoin amino acid as N(O)-butyldimethylsilyl derivatives in amino acid sequencing with methylisothiocyanate (Methylisothiocyanate를 이용한 아미노산 배열결정시 N(O)-butyldimethylsilyl 유도체로서의 methylthiohydantoin 아미노산의 기체 크로마토그래피에 의한 분석)

  • Woo, Kang-Lyung
    • Applied Biological Chemistry
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    • v.35 no.2
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    • pp.132-138
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    • 1992
  • For effective determination of methylthiohydantoin amino acids(MTHs) by gas liquid chromatography in the protein sequencing, derivatization with N-methyl-N-(tert.-butyl-dimethylsilyl)trifluoroacetamide(MTBSTFA), a new silylating reagents, was attempted instead of trimethylsilyl(TMSi) derivatives by N,O-bis(trimethylsilyl)trifluoroacetamide(BSTFA) used up to the present and N(O)-butyldimethylsilyl MTHs derivatized by MTBSTFA were analysed on HP-1 capillary column. Twenty one protein amino acids except cystine were indentified. Especially arginine that did not detected with TMSi derivative on packed column until now was resolved by derivatization with MTBSTFA. N(O)-butyldimethylsilyl MTHs showed multiple peaks by MTBSTFA were proline, isoleucine, glycine and tyrosine and hydroxyproline especially showed several extraneous peaks more than two. Calibration curves of N(O)-butyldimethysilyl MTHs of amino acids in the range of $2.5\;nmol{\sim}7.5\;nmole$ showed good linearity. however, those of lysine, histidine and arginine showed linearity in the range of $5.0\;nmole{\sim}15.0\;nmole$. Correlation coefficients and regression coefficients of all calibration curves were highly significant(p<0.001).

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Deletion of N-terminal End Region of ErmSF Leads to an Amino Acid Having Important Role in Methyl Transfer Reaction (ErmSF에서 특이적으로 발견되는 N-terminal End Region의 점차적인 제거에 의한 활성에 중요한 아미노산의 규명)

  • Lee Hak Jin;Jin Hyung Jong
    • Korean Journal of Microbiology
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    • v.40 no.4
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    • pp.257-262
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    • 2004
  • ErmSF is one of the ERM proteins which transfer the methyl group to A2058 in 23S rRNA to confer the resis­tance to MLS (macrolide-lincosamide-streptogramin B) antibiotics on microorganism. Unlike other ERM pro­teins, ErmSF contains long N-terminal end region (NTER), of which $25\%$ is composed of arginine that is known to interact with RNA well. Gradual deletion of NTER leaded us to the point where mutant protein lost much of activity in vivo. Overexpressed and purified mutant protein showed much reduced activity in vitro: $2\%$ activity relative to that of wild type protein. This fact suggests that this amino acid interact with RNA close to meth­ylatable adenine to locate it at an active site properly.

Numerical study of double diffusive convection due to lateral heating in a rotating annulus (회전하는 환형용기내의 옆면 가열에 의한 이중확산대류에 관한 수치해석)

  • Gang, Sin-Hyeong;Lee, Gyo-Seung;Lee, Jin-Ho
    • Transactions of the Korean Society of Mechanical Engineers B
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    • v.21 no.11
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    • pp.1422-1436
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    • 1997
  • Numerical investigations were conducted to study the convective phenomena of an initially stably stratified salt water solution with lateral heating in a uniformly rotating annulus. The method of investigation is the finite difference analysis of the basic conservation equation for an axisymmetric, unsteady, double-diffusive convection and calculation is made for R $a_{\eta}$=2*10$^{5}$ and Ta=10$^{7}$ ~ 2.5*10$^{8}$ . Formation of layered flow structure, merging process of layers, the corresponding temperature and concentration distributions, Nu variation with time are examined. Numerical results show that in each layer, the temperature profile looks 'S'-shaped and the concentration profile is uniform due to the convective mixing. At the interface between adjacent layers, the temperature changes smoothly but the concentration changes rapidly. As the effect of the rotation increases, the generation of rolls at hot wall, the formation and merging of layers are delayed. The average Nu shows the trend of conduction heat transferees the effect of the rotation increases.n increases.

A Study on the Silicidation of Thick Co/Ti Bilayer (두꺼운 이중층 Co/Ti 막의 실리사이드화에 관한 연구)

  • 이병욱;권영재;이종무;김영욱
    • Journal of the Korean Ceramic Society
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    • v.33 no.9
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    • pp.1012-1018
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    • 1996
  • To investigate the final structures and reactions of silicides a somewhat thick Ti monolayer Co monolayer and Co/Ti bilayer films were deposited on single Si(100) wafer by electron beam evaporation followed by heat treatment using RTA system in N2 ambient. TiO2 film formed between Ti and TiSi2 layers due to oxgen or moisture in the Ti monolayer sample. The final layer structure obtained after the silicidation heat-treatment of the Co/Ti bilayer sample turned out to be TiSi2/CoSi2/Ti-Co-Si alloy/CoSi2/Si sbustrate. This implies that imperfect layer inversion occurred due to the formation of Ti-Co-Si intermediate phase.

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Pyran and Pyridine as Building Blocks in Heterocyclic Synthesis (이중고리 합성에 블록제로서 이용된 피란과 피리딘)

  • El-Hashash, Maher.A.;El-Sawy, Abdallah.A.;Eissa, Abdelmonem.M.F.
    • Journal of the Korean Chemical Society
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    • v.53 no.3
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    • pp.308-324
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    • 2009
  • The present work is devoted to study the interaction of $\beta$-aroylacrylic acid derivative (3) with malononitrile in (DMF) in the presence of piperidine and/or ammonium acetate, then using the formed compounds as starting materials for synthesizing fused and isolated heterocyclic systems. It has been established that the $\beta$-aroylacrylic acid (3) reacts with malononitrile in (DMF) in the presence of piperidine as a catalyst with the formation of 4H-pyran derivative (4). By changing the catalyst into ammonium acetate, pyridine derivative (5) has been obtained. Also the N-maleamic acid derivatives (19) and (27) have been synthesized via the interaction of (4) and (5) with maleic anhydride. The purpose of this step is to study the behavior of the formed maleamic acid derivatives – as analogies of $\beta$-aroylacrylic acids – towards different active methylene compounds under Michael addition reaction.