• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
• /
• 1999.05a
• /
• pp.133-136
• /
• 1999

We report on the electrochemical properly of LiZ $n_{x}$Mn $_{2-x}$ $O_4$ for different degrees of Zn substitution(x) Though all cathode material showed spinel phase based on cubic phase in X-ray diffraction, other peaks(M $n_2$ $O_3$ or M $n_3$ $O_4$) gradually exhibited and became intense with the increase of x vague in LiZ $n_{x}$Mn $_{2-x}$ $O_4$. In addtion, TG-DTA analysis exhibited that both LiM $n_2$ $O_4$ and LiZ $n_{0.1}$ M $n_{1.9}$ $O_4$ occurred the weight loss(TG) and the endothermic and exothermic reaction(DTA) until 80$0^{\circ}C$ When x=0.1 in LiZ $n_{x}$Mn $_{2-x}$ $O_4$ cathode materials showed the charge and discharge capacity of about 100mAh/g at first cycle and about 70mAh/g after tooth cycle.cle.e.cle.e.e.e.

• Journal of Plant Biology
• /
• v.29 no.1
• /
• pp.53-65
• /
• 1986

The montane forests of Ulreung Island, Korea, were investigated by the ZM school method. By comparing the montane forests of this island with those of Korean Peninsula and of Japan, a new order, F a g e t a l i a m u l t i n e r v i s, a new alliance, F a l g i o n m u l t i n e r v i s, a new association, H e p a t i c o-F a g e t u m m u l t i n e r v i s and Rhododendron brachycarpum-Pinus parviflora community were recognized. The H e p a t i c o - F a g e t u m m u l t i n e r v i s was further subdivided into four subassociations; Subass. of Sasa kurilensis, Subass. of Rumohra standishii, Subass. of Rhododendron brachycarpum and Subass. of typicum. Each community was described in terms of floristic, structural and environmental features.

• Honam Mathematical Journal
• /
• v.35 no.2
• /
• pp.303-310
• /
• 2013

In this paper, we first show that $z_{{\kappa}X}:E_{cc}({\kappa}X){\rightarrow}{\kappa}X$ is $z^{\sharp}$-irreducible and that if $\mathcal{G}(E_{cc}({\beta}X))$ is a base for closed sets in ${\beta}X$, then $E_{cc}({\kappa}X)$ is $C^*$-embedded in $E_{cc}({\beta}X)$, where ${\kappa}X$ is the extension of X such that $vX{\subseteq}{\kappa}X{\subseteq}{\beta}X$ and ${\kappa}X$ is weakly Lindel$\ddot{o}$f. Using these, we will show that if $\mathcal{G}({\beta}X)$ is a base for closed sets in ${\beta}X$ and for any weakly Lindel$\ddot{o}$f space Y with $X{\subseteq}Y{\subseteq}{\kappa}X$, ${\kappa}X=Y$, then $kE_{cc}(X)=E_{cc}({\kappa}X)$ if and only if ${\beta}E_{cc}(X)=E_{cc}({\beta}X)$.

• Restorative Dentistry and Endodontics
• /
• v.8 no.1
• /
• pp.155-159
• /
• 1982

The author has studied comparatively the sealing quality of conventional Z.O.E. cement, chloropercha and FR cement by means of penetration of 2% methylene blue solution through the apex of human teeth in 112 cases as the time elapsed. The results were as follows; 1. All the specimen, of which dye immersion time is three days, showed dye penetration of low degree unrelated to the kinds of root canal cement and the degree of dye penetration was increased as the time elapsed. 2. Of all the experimental group, the Z.O.E. cement group showed the lowest degree of dye penetration and the FR filling group showed the highest degree of dye penetration. 3. The degree of dye penetration of FR cement group was higher than that of the Z.O.E. cement group but lower than that of the chloropercha group.

• Restorative Dentistry and Endodontics
• /
• v.6 no.1
• /
• pp.77-81
• /
• 1980

The author has studied comparatively the sealing quality of conventional Z.O.E. cement, Kerr sealer and Nogenol sealer by means of penetration of 2% methylene blue solution through the root apex of human teeth in 72 cases as time elapsed. The results were as follows; 1. All the specimens, whose dye immersion time is two days, showed dye penetration of low degree unrelated to the kinds of root canal sealer. 2. Kerr sealer group, like conventional Z.O.E. group, showed dye penetration of high degree related to increased time of immersion in the dye. 3. In Nogenol group, there was slight increase in penetration related to increased time of immersion in the dye. 4. Kerr sealer group showed comparatively lower grade of dye penetration than conventional Z.O.E. and higher than Nogenel sealer.

• Bulletin of the Korean Chemical Society
• /
• v.20 no.5
• /
• pp.539-542
• /
• 1999

The diastereoselectivity in the photocyclization of α-(o-ethylphenyl)acetophenone(1) to 1-methyl-2-phenyl-2-indanol was studied in zeolites X and Y, and compared with that in isotropic solvents. The yields of E-diastereomer at the irradiation of 1 in protic solvents were higher than those in aprotic solvents. The ratios of E-diastereomer to Z-diastereomer in zeolites X and Y were much higher than those in isotropic solvents. The E/Z ratios at the irradiation of 1 in zeolites X were also found to be dependent on the cations present. As the cation size increased from Li+ to Cs+, the ratio decreased. However, any pattern in the E/Z ratios was not found in zeolites Y. The diastereoselectivity observed in the zeolites was interpreted by the conformational restriction imposed by the cavity size. An efficient oxidation of 1 in zeolites RbX and CsX was also observed.

• Archives of Pharmacal Research
• /
• v.9 no.4
• /
• pp.237-242
• /
• 1986

The Synthesis of E, E, E-12-fluorofarnesol and E, Z-6-fluorofarnesol which are key intermediates for the study of biosynthesis of some sesquiterpenes, is described. E, E-Farnesyl acetate is treated with selenium dioxide to give E, E, E-12-hydroxy farnesyl acetate, whih is transformed by DAST into E, E, E-12-hydroxy farnesyl acetate, which is transformed by DAST into E, E, E,-12-fluorofarnesylacetate. The latter compound is hydrolyzed to E, E, E,-12-fluorofarnesol. The reformatsky reaction of 6-methyl-5-hepten-2-one with ethyl bromofluoroacetate affords ethyl 2-fluoro-3-hydroxy-3, 7 dimethyl-6-octanoate. This ester is acetylated and eliminated to give ethyl (Z)-2-fluoro-3, 7-dimethylocta-2, 6-dienoate, which is transformed to allyl bromide via allylic alcohol. The allyl bromide is treated with dianion of methyl acetate to give-keto ester. The $\beta$-keto ester is converted to diethyl phosphoryloxy compound. The conjugate addition of lithium dimethylcuprate to the latter compound gives fluoro ester, which is treated with DIBAL to afford E, Z-6-fluorofarnesol.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
• /
• 1999.11a
• /
• pp.594-597
• /
• 1999

The new green and red phosphors for PDP application activated by T $b^{3+}$ and E $u^{3+}$ were synthesized, and their photoluminance properties were investigated. It was found that the brightness of $Al_3$Gd $B_4$ $O_{12}$ :T $b^{3+}$ green phosphor under 147nm VUV irradiation was higher than that of commercial Z $n_2$ $SiO_4$:M $n^{2+}$ phosphor. But the emitting intensity of A1$_3$Gd $B_4$ $O^{12}$ :E $u^{3+}$ red phosphor was inferior to the commercial (Y,Gd)B $O_3$:E $u^{3+}$. $Al_3$Gd $B_4$ $O_{12}$ Phosphor had a strong excitation band at 160nm associated with the host absorption, and also the photoluminance excitation intensity of $Al_3$Gd $B_4$ $O_{12}$ :T $b^{3+}$ was higher than that of Z $n_2$ $SiO_4$:M $n^{2+}$, but the intensity of $Al_3$Gd $B_4$ $O_{12}$ :E $u^{3+}$ phosphor was smaller than (Y,Gd)B $O_3$:E $u^{3+}$ phosphor In the VUV range. C $e^{3+}$ co-doping in A1$_3$Gd $B_4$ $O^{12}$ :E $u^{3+}$ and substitution of $Al^{3+}$ by G $a^{3+}$ A1$_3$Gd $B_4$ $O^{12}$ :E $u^{3+}$ phosphor were tried, but they did not improved the optical property .d the optical property .ty .

• Bulletin of the Korean Chemical Society
• /
• v.33 no.10
• /
• pp.3253-3257
• /
• 2012

Second-order rate constants for the reactions of phenyl Y-substituted-phenyl carbonates 5a-g with Z-substituted-phenoxides ($k_{Z-PhO^-}$) have been measured spectrophotometrically in 80 mol % $H_2O$/20 mol % DMSO at $25.0{\pm}0.1^{\circ}C$. 4-Nitrophenyl phenyl carbonate (5e) is up to 235 times more reactive than 4-nitrophenyl benzoate (4e). The Br$\o$nsted-type plot for the reactions of 5e with Z-substituted-phenoxides is linear with ${\beta}_{nuc}=0.54$, which is typical for reactions reported previously to proceed through a concerted mechanism. Hammett plots correlated with ${\sigma}^o$ and ${\sigma}^-$ constants for the reactions of 5a-f with 4-chlorophenoxide exhibit highly scattered points. In contrast, the Yukawa-Tsuno plot results in an excellent linear correlation with ${\rho}_Y=1.51$ and r = 0.52, indicating that the leaving-group departure occurs at the rate-determining step (RDS). A stepwise mechanism, in which leaving-group departure occurs at RDS, has been excluded since the incoming 4-$ClPhO^-$ is more basic and a poorer nucleofuge than the leaving Y-substituted-phenoxides. Thus, the reaction has been concluded to proceed through a concerted mechanism. Our study has shown that the modification of the nonleaving group from benzoyl to phenyloxycarbonyl causes a change in the reaction mechanism (i.e., from a stepwise mechanism to a concerted pathway) as well as an increase in the reactivity.

• Journal of the Korean Ceramic Society
• /
• v.37 no.10
• /
• pp.962-967
• /
• 2000

산소 결핍 페라이트 (oxygen deficient ferrites, ODF) MF $e_2$ $O_{4-}$$\delta$/는 약 30$0^{\circ}C$의 낮은 온도에서 온실가스중 하나인 $CO_2$를 C와 $O_2$로 분해시킨다. 본 연구에서는 $CO_2$분해 촉매로서 3원계 초미세 페라이트 N $i_{x}$Z $n_{1-x}$F $e_2$ $O_4$와 N $i_{x}$ $Co_{1-x}$F $e_2$ $O_4$를 수열합성법과 공침법 등의 습식 합성법으로 각각 합성하여 이들 분말의 특성과 $CO_2$분해 특성을 고찰하였다. 페라이트의 XRD 결과, 결정구조는 모두 전형적인 스피넬 구조로 동일하게 나타났다. BET 비표면적은 수열합성법으로 제조한 3원계 페라이트의 경우 110$m^2$/g 이상으로 공침법으로 제조한 페라이트보다 비교적 큰 값을 나타냈고 분말 입자크기 또한 약 10nm의 매우 미세한 분말을 얻을 수 있었다. 3원계 산소 결핍 페라이트의 $CO_2$분해 효율은 공침법으로 합성한 것보다 수열합성법으로 합성한 것이 더 우수하게 나타났으며, N $i_{x}$ $Co_{1-x}$F $e_2$ $O_{4-}$$\delta$/보다 N $i_{x}$Z $n_{1-x}$F $e_2$ $O_{4-}$$\delta$/가 우수한 것으로 나타났다.