• Archives of Pharmacal Research
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• 제12권1호
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• pp.42-47
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• 1989

From the roots of Puisatiila koreana, three monodesmosides(pulsatilla saponins A, B and D) and two bisdesmosides(pulsatilla saponins F and H) were isolated. The structure of these saponins have been determined as hederagenin 3-O-${\beta}$-L-rhamnopyranosyl($1{\to}2$)- ${\alpha}$-L-arabinopyranoside(A), hederagenin 3-O-${\beta}$-D-glucopyrano syl($1{\to}4$) - ${\alpha}$-L-arabinopyranoside(B), hederagenin 3-O- ${\alpha}$-L-rhamnopyranosyl ($1{\to}2$)-[${\beta}$-D-glucopyranosyl($1{\to}4$]-${\alpha}$-L-arabinopyranoside(D), 3-O-${\alpha}$-L-rhamnopyranosyl($1{\to}2$)-{${\alpha}$-L-arabinopyranosyl hederagenin 28-O-${\alpha}$-L-rhamnopyrano syl($1{\to}4$)-${\beta}$-D-glucopyrano syl($1{\to}6$)-${\beta}$-D-glucopyranosyI ester (F) and 3-O-${\alpha}$-L-rhamnopyranosyl($1{\to}2$)-[${\beta}$-D-glucopyranosyl($1{\to}4$)]- ${\alpha}$-L-arabinopyranosyl hederagenin 28-O-${\alpha}$-L-lharnnopyranosyl($1{\to}4$)-${\beta}$-D-glucopyranosyl($1{\to}6$)-${\beta}$-D-glucop yranosyl ester(H) on the basis of chemical and spectral studies. Pulsatilla saponin B is the first report of its presence in plants but saponins A, D, F, and H have recently been isolated from the same genus p. cernua.

• The Korean Journal of Ceramics
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• 제4권3호
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• pp.204-206
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• 1998

The Gibbs free energy of formation of $BaThO_3$ from elemental oxides has been measured at temperatures between 853 and 903 K using a $CaF_2$ solid electrolyte galvanic cell. The galvanic cell consisted of Pt, $O_2, CaO+CaF_2 \parallel CaF_2 \parallelBaThO_3+ThO_2+BaF_2, O_2$, Pt EMF gave the standard Gibbs free energy for the reaction $CaF_2+BaThO_3=CaO+BaF_2+ThO_3$ as $\DeltaG^o$,/TEX>=124111.031-117.597 T(J/mol).

• 한국자기학회지
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• 제13권1호
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• pp.36-40
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• 2003

D $y_{x}$B $i_{3-x}$F $e_{5}$ $O_{12}$(x=0.5,1.0,1.5,2.0) 가네트 박막을 sol-gel법의 일종인 Pechini법의 이용하여 $Al_2$ $O_3$, G $d_3$G $a_{5}$ $O_{12}$ (111) 평면에 성장시켰다. 단일 조성의 D $y_{x}$B $i_{3-x}$F $e_{5}$ $O_{12}$ 박막을 얻기 위한 열처리 온도는 기판의 종류에 의존하며, 박막과 같은 구조의 G $d_3$G $a_{5}$ $O_{12}$ (111) 기판의 경우 A1$_2$ $O_3$ 기판을 사용한 경우에 비해 단일 조성을 얻기 위한 열처리 온도가 약 5$0^{\circ}C$ 감소함을 알 수 있었다. G $d_3$G $a_{5}$ $O_{12}$ (111) 기판 위에 성장된 가네트 박막의 낟알들은 대부분 기판과 같은 [111] 방향으로 정렬하며, 이 경우 박막의 자기 이력 곡선은 5000 Oe 이상에서도 포화 자기화에 도달하지 못하는 것으로 확인되었다. 이러한 현상의 원인으로 회전 자기화 과정 (rotation magnetization process)에 의한 것으로 추정하였다. Pechini 법으로 성장시킨 D $y_{x}$B $i_{3-x}$F $e_{5}$ $O_{12}$ 박막에서 단위 세포 당 최대 Bi 이온의 양은 2.0 이하임을 처음으로 확인하였고, 이는 LPE법에 의해 성장된 단결정 가네트의 경우에 알려진 최대 Bi이온의 양 2.3보다 작은 값이다.에 알려진 최대 Bi이온의 양 2.3보다 작은 값이다.은 값이다.

• 대한화학회지
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• 제55권3호
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• pp.405-411
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• 2011

Methyl hydro-peroxide의 methyl group과 O-H에 F를 치환 시킨 fluoromethyl fluoroperoxide($CH_nF_{3-n}OOF$)의 안정한 conformers와 isomers에 대하여 MP2/6-311G(d,p) 방법과 B3LYP/6-311++G(d,p) 방법으로 최적화 계산을 수행하였고 vibrational frequencies를 구하였다. $CH_3OOF$와 $CH_2FOOF$, $CHF_2OOF$, $CF_3OOF$ 분자 모두 가장 안정한 형태는 skew 구조로 나타났으며 $CH_3OOH$와 비교할 때 대단히 짧은 O-O 결합길이를 갖는다. Trans, cis conformers의 경우 skew 형태보다 8-12 kcal/mol 정도 높은 에너지를 갖으며 O-O 결합길이는 훨씬 길어진다. $CH_2FOOF$, $CHF_2OOF$, $CF_3OOF$ 분자들은 methyl group의 F에 의한 induction 효과로 짧은 C-O 결합길이를 갖고 O-F 결합길이는 길어지나 치환된 F 원자의 수에 따른 구조변화는 그리 크지 않다.

• 한국방사선학회논문지
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• 제9권1호
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• pp.39-45
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• 2015

본 연구는 고상법으로 형광체를 합성하였다. 모체 물질은 $La_2W_3O_{12}$에 활성제로 $Eu^{3+}$이온을 첨가하여 활성제 조성변화에 따른 XRD 분석과 여기 및 방출 스펙트럼 및 온도에 따른 형광 스펙트럼 분석과 수명시간을 측정하였다. $La_2W_3O_{12}:Eu^{3+}$의 1 mol%의 XRD 스펙트럼은 ICSD 카드 (78180)에 보고된 데이터 스펙트럼과 비교하였을 때 XRD 스펙트럼이 잘 일치함을 확인 하였다. $La_2W_3O_{12}$ 형광체에 활성제로 $Eu^{3+}$이온 1 mol%를 첨가한 여기 스펙트럼에서는 286 nm 근처에서 286 nm 넓은 전하전달밴드가 관찰된다. 이 전하전달밴드는 $WO_4$그룹과 $Eu^{3+}$이온의 전하 전달 밴드이며 $O^{2-}-W^{6+}$, $O^{2-}-Eu^{3+}$의 ligand-to-metal 전하 전달 흡수가 이루어진다. 350~500 nm 영역에서는 $Eu^{3+}$의 f-f 전이에 의한 피크가 나타났다. 여기 스펙트럼에서 $Eu^{3+}$의 $^7F_0{\rightarrow}{^5D_4},{^5D_4},{^5L_6},{^5G_4},{^5D_3},{^5D_2}$ 전이에 해당한다. 방출 스펙트럼은 280, 395 nm로 각각 여기한 결과 $Eu^{3+}$이온의 $^5D_0{\rightarrow}^7F_2$(618nm)에서 강한 피크가 보였다. 희토류 이온이 도핑 되지 않은 $La_2W_3O_{12}$ 형광체를 266 nm로 여기하여 온도에 변화 따른 방출 스펙트럼은 저온에서 상온으로 갈수록 형광의 세기가 약하게 나타났다. 온도에 따른 수명시간은 7 K($114{\mu}s$), 100 K($94{\mu}s$), 200 K($10{\mu}s$), 300 K($0.5{\mu}s$)로 나타났다.

• 천문학논총
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• 제8권1호
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• pp.119-136
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• 1993

Optimum hypering conditions are found for IIIa-J, IIIa-F, 103a-O, 103a-D, and IIa-O plates using hypersensitization machine in KAO. For every experimental plate we get speed gain, fog increment, signal to noise ratio and relative DQE according to hypering time and temperature. The hypersensitization method is baking with 8% hydrogen mixed gas. For IIIa-J, 103a-O, and 103a-D plates treated $65^{\circ}C$, 3 hours baking, the speed gains arc increased by about 10 times, 2 times, and 2 times compared to untreated plates, respectively. The fogs are increased by 0.08, 0.10, and 0.08, respectively. For IIIa-F, IIa-O plates treated $65^{\circ}C$, 2 hours baking, the speed gains are increased by about 4.7 times and 1.8 times compared to untreated plates, respectively. The fogs are increased by 0.15 and 0.04, respectively.

• 반도체디스플레이기술학회지
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• 제16권4호
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• pp.86-90
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• 2017

$Tb^{3+}$ or $Eu^{3+}$ or $Ce^{3+}$-doped $CaYAlO_4$ phosphor were synthesized by solid-state method. $CaYAlO_4:Tb^{3+}$ is shown that the $Tb^{3+}$-doping concentration has a significant effect on the $^5D_4/^5D_3{\rightarrow}7F_J$ (J=6,...,0) emission intensity of $Tb^{3+}$. The $CaYAlO_4:Tb^{3+}$ phosphors show tunable photoluminescence from blue to yellow with the change of doping concentration of $Tb^{3+}$ ions. The $CaYAlO_4:Eu^{3+}$ phosphors exhibit a red-orange emission of $Eu^{3+}$ corresponding to $^5D_0$, $_{1,2}{\rightarrow}^7F_J$ (J=4,...,0) transitions. The $CaYAlO_4:Ce^{3+}$ phosphors show a blue emission due to $Ce^{3+}$ ions transitions from the 5d excited state to the $^2F_{5/2}$ and $^2F_{7/2}$ ground states. The decay time of $CaYAlO_4:Tb^{3+}$ phosphors decrease from 1.33 ms to 0.97 ms as $Tb^{3+}$ concentration increases from 0.1 mol% to 7 mol%. The decay time of $CaYAlO_4:Eu^{3+}$ phosphors increase from 0.94 ms to 1.17 ms as $Eu^{3+}$ concentration increases from 1 mol% to 9 mol%.

• 대한화학회지
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• 제43권1호
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• pp.52-57
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• 1999

In($C_6F_5)_3{\cdot}D(D=CH_3CN$, O($C_2H_5)_2$)와 ($CH_3)_3SiC_6F_5$/CsF, $C_6F_5$MgBr 또는 Cd($C_6F_5)_2$을 반응시켜 [In($C_6F_5)_4$]- 음이온 화합물을 합성하였으나, 이들 indium(III) 음이온 화합물들은 온도에 민감하고 습기에 대해 불안정하다. 안정한 indium(III) 음이온 착물은 PNPCl(PNP=bis(triphenylphosphino)ammonium)과의 양이온 치환반응시켜 얻었으며, 관 크로마토 그래피를 이용하여 분리 정제하였다. 합성된 화합물의 특성은 핵자기 공명 분석법, 적외선 분광분석법, 분자량 측정, DTA/TG 그리고 원소분석법을 이용하여 조사하였다.

• 한국응용과학기술학회지
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• 제17권2호
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• pp.67-75
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• 2000

Cosmetic industries have recently developed sun-block products, which are composed of W/O or O/W emulsion system. It was very difficult for waterproofing product to show the stability in W/O emulsion with $TiO_{2}$. To enhance the stability of W/O emulsion, it needs to be combined with the water and oil soluble components as the gelling agents. The emulsifiers used in W/O were 3.0% of cetyl dimethicone copolyol, 2.0% of sorbitan sesquioleate as the basic emulsifiers, and 0.6% of quaternium-18 bentonite and 1.5% of dextrin palmitate as stabilizer were used. The content of titanium dioxide was optimized up to 8.0%. Titanium dioxide was used as the UV scattering powder coated with $Al_{2}O_{3}$(UV-sperse T40/TN). The sunscreen cream prepared with W/O emulsion system by using QB and DP showed higher stability than that of W/O emulsion system by using each QB and DP. W/O emulsion from Formula 3 for passing one year was very durable more than F1 and F2. Within W/O emulsion by observing F1, F2 and F3 for one year, F3 was more excellent than F2 and F3 when they were observed at RT, $4^{\circ}C$, $40^{\circ}C$, because F3 used the mixed QB and DP in W/O emulsion. The zeta potential for F1, F2, and F3 after one year were 21, 30 and 43, respectively. From these result F3 was found best stable emulsion. The in-vitro SPF value for F3 was 35 for the initial product at room temperature and also, the in-vitro SPF values of F3 was 32 for after one year. Finally, the mean in-vivo SPF value of 10 volunteers for F3 was 27.3 by the Korea cosmetic association made the rules of SPF.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제45회 하계 정기학술대회 초록집
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• pp.270.1-270.1
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• 2013

Zinc oxide (ZnO) is one of the most powerful materials for purifying organic pollutants using photocatalytic activity. In this study, we have introduced a novel method to design highly photoreactive flexible 3 dimensional (3D) ZnO nanocomposite [F-ZnO-m (m: reaction time, min)] by electrospinning and simple-step ZnO growth processing (one-step ZnO seed coating/growth processing). Significantly, the F-ZnO-m could be a new platform (or candidate) as a photocatalytic technology for both morphology control and largearea production. The highest photocatalytic degradation rate ([k]) was observed for F-ZnO-m at 2.552 h-1, which was 8.1 times higher than that of ZnO nanoparticles (NPs; [k] = 0.316 h-1). The enhanced photocatalytic activity of F-ZnO-m may be attributed to factors such as large surface area. The F-ZnO-m is highly recyclable and retained 98.6% of the initial decolorization rate after fifteen cycles. Interestingly, the F-ZnO-m samples show very strong antibacterial properties against both Gram-negative Escherichia coli (E. coli) and Gram-positive Staphylococcus aureus (S. aureus) after exposure to UV-light for 30 min. The antibacterial properties of F-ZnO-m samples are more effective than those of ZnO NPs. More than 96.6% of the E. coli is sterilized after ten cycles. These results indicate that F-ZnO-m samples might have utility in several promising applications such as highly efficient water/air treatment and inactivation of pathogenic microorganisms.