• 제목/요약/키워드: $NaMnO_2$

검색결과 339건 처리시간 0.028초

Kinetic Studies on the Reaction of the Heterobimetallic Anion, $(OC)_5CrMn(CO)_5{^-}M^+\;(M^+=Na^+,\;PPN^+)$ with Allyl Bromide

  • Park, Yong K.;Kim, Gyu S.;Song, Gwan O.
    • Bulletin of the Korean Chemical Society
    • /
    • 제16권4호
    • /
    • pp.310-315
    • /
    • 1995
  • The heterobimetallic anion, (OC)5CrMn(CO)5-M+ (M+=Na+, PPN+), which has a donor-acceptor metal-metal bond1, was reacted with allyl bromide to yield BrCr(CO)5- and Mn(CO)5(CH2CHCH2). The reaction mechanism has been proposed in terms of the consecutive reaction pathway in which Cr(CO)5(THF) is an important intermediate leading to the corresponding product. Counterion effect on this reaction was also evaluated and the results were compared with those of the corresponding reaction of the mononuclear carbonyl anion, Mn(CO)5-.

$Mn_3O_4$의 합성과 $CO_2$ 분해 및 흡착에 관한 연구 (A Study on the Synthesis of $Mn_3O_4$ and the Decomposition and Adsorption of $CO_2$)

  • 김승호;박영구;고재철
    • 한국가스학회지
    • /
    • 제4권2호
    • /
    • pp.27-32
    • /
    • 2000
  • 본 연구는 염화망간과 수산화나트륨을 이용하여 당량비에 따라 산화망간을 합성하였다. 합성된 산화망간의 결정구조와 비표면적을 측정하였으며, 이산화탄소의 분해 및 흡착에 대하여 연구하였다. 합성된 시료의 결정구조 분석결과 $Mn_3O_4$의 주피크가 나타났으며, 약간의 $MnO_2$$Mn_5O_8$도 관찰되었다. 또한 비표면적은 $13.92m^2/g{\~}32.33m^2/g$으로 측정되었다. 산화망간을 이용하여 $450^{\circ}C$에서 이산화탄소의 분해를 실시하였으며, 당량비 0.75에서 가장 잘 분해되었다. 이산화탄소의 화학흡착량을 측정한 결과 2.885cc/g${\~}$19.628cc/g으로 관찰되었으며, 이산화탄소의 흡착을 위한 최적당량비는 1.00이었다.

  • PDF

토끼 심방근 및 혈관 평활근에서의 $Na^{+}/Ca^{2+}$ 교환기전에 관한 연구 ($Na^{+}/Ca^{2+}$ Exchange System in Atrial Trabeculae and Vascular Smooth Muscle of the Rabbit)

  • 김희주;문형로;엄융의;호원경
    • The Korean Journal of Physiology
    • /
    • 제22권1호
    • /
    • pp.13-29
    • /
    • 1988
  • In order to elucidate the regulatory mechanism of intracellular calcium ion concentrations, contractions or contractures induced by $Na^{+}-removal$, calcium-application or ouabain-treatment as an index of $Na^+/Ca^{2+}$ exchange activity were studied in atrial muscle or vascular smooth muscle (aorta and renal artery) of the rabbit. The magnitude of low sodium contractures in atrial trabeculae increased with sigmoid shape when external sodium concentrations were reduced to sodium-free condition, whereas that of calcium contracture intensified in a parabolic pattern when external calcium concentrations were elevated to 8 mM. $Na^{+}-removal$ contractures were induced in a duration-dependent manner to $K^{+}-free$ exposure and same findings were observed with ouabain treatment. $Na^{+}-free$ contractures were not affected by verapamil treatment, but stimulated by $100{\mu}M\;Mn^{2+}$ and inhibited by high concentrations of $Mn^{2+}\;(2{\sim}8mM)$ in a dose-dependent manner. Ryanodine which is known to suppress the release of calcium from internal store abolished spontaneous twitch contractions induced by $K^{+}-free$ solution, but had no effect on the development $Na^{+}-free$ contractures. Na-free contractures were not always induced in vascular smooth muscle preparations. Contractures by $O\;mM\;Na^+$ were usually seen in aorta, but not often in renal artery.$50\;mM\;K^+$, noradrenaline (NA) and angiotensin II (AII) always evoked very large contraction in all preparations of vascular smooth muscle. Contractures developed by $O\;mM\;Na^+$ were not sensitive to verapamil treatment as in atrial trabeculae, but were abolished by $100{\mu}M\;Mn^{2+}$. In contrast to $Na^{+}-free$ contractures, $Mn^{2+}(100{\mu}M)$ had no effect on the contractures induced by NA or 50 mM$K^+$. Caffeine in the concentration of 10 mM evoked transient contracture in the distal renal artery. The rate of spontaneous relaxation in caffeine contracture was dependent upon the concentrations of external sodium, and had double component of relaxation when the rate of relaxation was plotted in the semilogarithmic scale of relative tension versus time. Especially late components of relaxation had more direct relation to $Na^+$ concentrations. It could be concluded that $Na^+/Ca^{2+}$ exchange mechanism in the heart has a large capacity, inhibited by $Mn^{2+}$ but not by verapamil and ryanodine, while $Na^+/Ca^{2+}$ exchange system in vascular smooth muscle has a very low capacity especially in small artery, inhibited by low concentration of $Mn^{2+}\;(100{\mu}M)$ but not affected by verapamil and ryanodine.

  • PDF

Skaergaard 암체의 감람석의 성분변화 (Compositional Variation in Olivine in the Skaergaard Intrusion)

  • Jang, Yun-Deuk
    • 암석학회지
    • /
    • 제12권3호
    • /
    • pp.110-118
    • /
    • 2003
  • Skaergaard 암체의 감람석의 성분변화를 연구하기 위하여 Layered Series(LS), Upper Border Series (UBS), 및 Marginal Border Series(MBS)에서 산출되는 감람석의 성분을 분석하였다. 분화에 따른 원소조성변 화는 일반적으로 암체 전체에서 유사한 원소조성변화를 보여주는데 감람석의 FeO*, Ti $O_2$, 및 MnO는 증가하고, MgO와 $SiO_2$는 감소하고, $Na_2$O, $K_2$O, A1$_2$ $O_3$, CaO, 및 P$_2$ $O_{5}$는 분화에 따른 주목할 만한 변화를 보이지 않는다. 분화과정의 전반에 걸쳐 Skaergaard 감람석은 어떠한 급격한 원소 변화 또한 보여주지 않는다. 따라서 마그마 분화에 따라 Skaergaard의 감람석이 체계적인 원소조성변화를 보이는 것으로 Skaergaard 마그마 분화 도중에 새로운 마그마의 주입의 가능성은 배제된다. 주목할 만한 급격한 원소변화가 MnO에서 관찰된다. Layered Series(LS) 감람석의 MnO 성분은 분화가 진행됨에 따라 꾸준히 증가하다가 UZc에서 급격히 감소하는데, 유사한 경향이 UBS, 및 MBS에서도 관찰된다. 이와 같이 Skaergaard 마그마 분화 말기에 관찰되는 감람석의 MnO 성분의 급격한 변화는 liquidus상으로 갑자기 출현하는 ferrobustamite에 기인한다.

기계적 합금법을 이용한 리튬 2차 전지용 층상 양극물질 $Li[Ni_xCo_{1-2x}Mn_x]O_2$ 의 합성 및 전기화학적 특성에 관한 연구 (Synthesis and electrochemical properties of layered $Li[Ni_xCo_{1-2x}Mn_x]O_2$ materials for lithium secondary batteries prepared by mechanical alloying)

  • 박상호;신선식;선양국
    • 한국결정학회:학술대회논문집
    • /
    • 한국결정학회 2002년도 정기총회 및 추계학술연구발표회
    • /
    • pp.16-16
    • /
    • 2002
  • The presently commercialized lithium-ion batteries use layer structured LiCoO₂ cathodes. Because of the high cost and toxicity of cobalt, an intensive search for new cathode materials has been underway in recent years. Recently, a concept of a one-to-one solid state mixture of LiNO₂ and LiMnO₂, i.e., Li[Ni/sub 0.5/Mn/sub 0.5/]O₂, was adopted by Ohzuku and Makimura to overcome the disadvantage of LiNiO₂ and LiMnO₂. Li[Ni/sub 0.5/Mn/sub 0.5/]O₂ has the -NaFeO₂ structure, which is characteristic of the layered LiCoO₂ and LiNiO₂ structures and shows excellent cycleability with no indication of spinel formation during electrochemical cycling. Layered Li[Ni/sub x/Co/sub 1-2x/Mn/sub x/]O₂ (x = 0.5 and 0.475) materials with high homogeneity and crystallinity were synthesized using a mechanical alloying method. The Li[Ni/sub 0.475/Co/sub 0.05/Mn/sub 0.475/]O₂ electrode delivers a high discharge capacity of 187 mAh/g between 2.8 and 4.6 V at a high current density of 0.3 mA/㎠(30 mA/g) with excellent cycleability. The charge/discharge and differential capacity vs. voltage studies of the Li[Ni/sub x/Co/sub 1-2x/Mn/sub x/]O₂ (x = 0.5 and 0.475) materials showed only one redox peak up to 50 cycles, which indicates that structural phase transitions are not occurred during electrochemical cycling. The magnitude of the diffusion coefficients of lithium ions for Li[Ni/sub x/Co/sub 1-2x/Mn/sub x/]O₂(x = 0.5 and 0.475) are around 10/sup -9/ ㎠/s measured by the galvanostatic intermittent titration technique (GITT).

  • PDF

Effect of MnO2 Addition on Microstructure and Piezoelectric Properties of 0.95(Na0.5K0.5)NbO3-0.05CaTiO3 Piezoelectric Ceramics

  • Kim, Jong-Hyun;Seo, In-Tae;Hur, Joon;Kim, Dae-Hyeon;Nahm, Sahn
    • 한국세라믹학회지
    • /
    • 제53권2호
    • /
    • pp.129-133
    • /
    • 2016
  • $MnO_2$ was added to the $0.95(Na_{0.5}K_{0.5})NbO_3-0.05CaTiO_3$ (NKN-CT) ceramics in order to promote the densification and improve the poling efficiency by increasing the resistance of the specimens. Densification and abnormal grain growth occurred in the $MnO_2$-added NKN-CT ceramics sintered at $1020^{\circ}C$, indicating that $MnO_2$ assisted the liquid-phase sintering of these materials. $Mn^{3+}$ ions were considered to enter the A-site of the matrix, thereby producing the free electrons, which interacted with the holes resulting from the evaporation of alkali ions. This interaction results in an increase in the resistance of the specimens. The increased resistance improved the poling efficiency and, hence, the dielectric and piezoelectric properties of the NKN-CT ceramics. A few of the $Mn^{3+}$ ions that entered the B-site of the NKN-CT matrix led to a slight increase in the mechanical quality factor.

산화제 NaOCl와 $H_2O_2$를 이용한 광산배수 정화에 관한 연구 (Studies on Purification of Mine Drainage with NaOCl and $H_2O_2$)

  • 최승원;장윤득;김영훈;김정진
    • 자원환경지질
    • /
    • 제43권1호
    • /
    • pp.21-31
    • /
    • 2010
  • 산화제를 이용한 광산배수 정화에 관한 연구를 위하여 옥동광산으로부터 채수한 갱내수와 침출수를 산화제인 NaOCl와 $H_2O_2$를 이용하여 반응 실험을 실시하였다. 초기 갱내수의 pH와 EC는 각각 5.77, 831 uS/cm 이며, Mg(23.25 mg/l), Mn(14.90 mg/l), Zn(22.99 mg/l)이다. 광미적치장으로부터 유출되는 침출수의 pH와 EC는 6.38, 1920 uS/cm이며, Mg(98.75 mg/l), Mn(3.38 mg/l), Zn(6.16 mg/l)로 갱내수와 다른 양이온 농도 특성을 갖는다. 산화제의 종류와 양에 따라 양이온이 제거 되는 데 소요되는 시간적 차이가 있지만, 갱내수와 침출수에 포함된 Mg, Zn, Mn은 99%이상 제거되었다. Visual MINTEQ 계산결과 포화지수가 0보다 큰 값을 나타내는 화합물이 존재하지 않기때문에 초기 갱내수와 침출수로부터 침전 가능한 광물은 존재하지 않는다. 갱내수와 광미적치장 침출수를 NaOCl과 반응시킬 때 생성되는 침전물은 적갈색의 Mangano-calcite이며, 그 외 Calcite magnesian, Calcite 등의 광물을 포함하고 있다.

담양 지역 음용 지하수에 형성된 망간 스케일에 대한 지구화학 (Geochemistry of Mn Scales Formed in Groundwater in the Damyang Area)

  • 박천영;김성구;신인현;안건상;김영인
    • 한국지구과학회지
    • /
    • 제27권3호
    • /
    • pp.313-327
    • /
    • 2006
  • 담양 지역의 음용 지하수 중에 형성된 망간 스케일의 지구화학적 특성을 규명하고자 하였다. 망간 스케일은 MnO 및 $SiO_2$로 구성되어 있고, MnO의 함량은 56.61wt.%에서 68.69wt.%, 그리고 $SiO_2$ 함량은 1.56wt.%에서10.45wt.%로 나타난다. 망간 스케일 중의 Ba와 Mo 함량은 지하수 심도가 증가할수록 증가하여 나타나고 Zn과 Pb는심도가 증가할수록 감소한다. 망간 스케일을 x-선 회절 분석을 한 결과 birnessite, 석영 및 장석이 분석되었다. IR 분석에서 망간 스케일은 OH, $H_2O$ 그리고 birnessite에 의한 흡수 밴드가 관찰된다. SEM 및 EDS 분석에서 망간 스케일은 포도송이 구조, 과립 구조, 구상 구조 및 속이 빈 straw 구조로 되어 있는 것이 관찰된다. 이들 구조들은 고농도의 망간함량에 의해 단순히 과포화로 침전되었을 것으로 생각되며, 혹은 Lepthothrix discophora에 의해 미생물적으로 침전되었을 것으로 생각된다. 이들 구조들의 표면을 EDS로 분석한 결과 Mn의 원자(atomic) 퍼센트가 28에서 44범위로 나타나고 Si, K, Na, Ca, Cl, Cu, Zn 및 Ba 등이 검출된다.

Synthesis of ZnS:Mn-Gly-C60 Nanocomposites and Their Photocatalytic Activity of Brilliant Green

  • Li, Jiulong;Ko, Weon Bae
    • Elastomers and Composites
    • /
    • 제53권2호
    • /
    • pp.75-79
    • /
    • 2018
  • ZnS:Mn-glycine (ZnS:Mn-Gly) nanocomposites were synthesized by capping ZnS:Mn nanocomposites with glycine. Zinc sulfate heptahydrate ($ZnSO_4{\cdot}7H_2O$), glycine ($C_2H_5NO_2$), manganese sulfate monohydrate ($MnSO_4{\cdot}H_2O$), and sodium sulfide ($Na_2S$) were used as the source reagents. $ZnS:Mn-Gly-C_{60}$ nanocomposites were obtained by heating the ZnS:Mn-Gly nanocomposites and fullerene ($C_{60}$) at a 2:1 mass ratio in an electric furnace at $700^{\circ}C$ for 2 h. X-ray diffraction (XRD) was used to characterize the crystal structure of the synthesized nanocomposites. The photocatalytic activity of the $ZnS:Mn-Gly-C_{60}$ nanocomposites was evaluated, via the degradation of brilliant green (BG) dye under 254 nm irradiation, with a UV-vis spectrophotometer.