• 한국재료학회지
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• 제9권11호
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• pp.1148-1152
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• 1999

본 연구에서는 기존에 알려진 구리 전구체와 새롭게 개발된 전구체인 hfac (hexafluoroacetylacetonate) Cu(I) DMB (3,3-dimethyl-1-butene)를 비교 평가해보았다. (Hfac)Cu(I) (DMB)의 증가압은 $40^{\circ}C$에서 3 torr 정도로 기존에 잘 알려진 (hfac)Cu(I) vinyltrimethylsilane (VTMS) 보다 10배 정도 높은 것으로 나타났으며 그럼에도 불구하고 상당히 안정하여 $65^{\circ}C$에서 일주일 이상 가열하여도 변하지 않았다. 이 전구체로 100-$280^{\circ}C$에서 구리 박막을 증착할 수 있었으며 150-$250^{\circ}C$온도 범위에서 2.0$\mu\Omega$-cm의 순수한 구리 박막을 얻었다. 구리 박막의 증착 속도는 기존의 전구체보다 7~8배 정도 높은 것으로 나타났다.

• Journal of Pharmaceutical Investigation
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• 제34권6호
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• pp.513-519
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• 2004

A sensitive method for quantification of pinaverium bromide in human plasma was established using liquid chromatography-electrospray ionization tandem mass spectrometry(LC-ESI-MS/MS). Glimepiride was used as internal standard. Pinaverium bromide and internal standard in plasma sample were extracted using tert-butylmethylether(TBME). A centrifuged upper layer was then evaporated and reconstituted with mobile phase of acetonitrile-5 mM ammonium formate (80/20, pH 3.0). The reconstituted samples were injected into a $C_{18}$ reversed-phase column. Using MS/MS with multiple reaction monitoring (MRM) mode, pinaverium and glimepirde were detected without severe interference from human plasma matrix. Pinaverium produced a protonated precursor ion $([M+H]^+)$ at m/z 510.3 and a corresponding product ion at m/z 228.9. Internal standard produced a protonated precursor ion $([M+H]^+)$ at m/z 491.5 and a corresponding product ion at m/z 352.0. Detection of pinaverium bromide in human plasma was accurate and precise, with limit of quantitation at 0.5 ng/ml. The method has been successfully applied to bioavailability study of pinaverium bromide tablet in Korean healthy male volunteers. Pharmacokinetic parameters such as $AUC_t,\;C_{max},\;T_{max},\;K_{el}\;and\;t_{1/2}$ were calculated.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제45회 하계 정기학술대회 초록집
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• pp.283.2-283.2
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• 2013

The variation of chemical and interfacial state during the growth of Ta2O5 films on the Si substrate by atomic layer deposition (ALD) was investigated using in-situ synchrotron radiation photoemission spectroscopy. A newly synthesized liquid precursor Ta(NtBu)(dmamp)2Me was used as the metal precursor, with Ar as a purging gas and H2O as the oxidant source. The core-level spectra of Si 2p, Ta 4f, and O 1s revealed that Ta suboxide and Si dioxide were formed at the initial stages of Ta2O5 growth. However, the Ta suboxide states almost disappeared as the ALD cycles progressed. Consequently, the Ta5+ state, which corresponds with the stoichiometric Ta2O5, only appeared after 4.0 cycles. Additionally, tantalum silicate was not detected at the interfacial states between Ta2O5 and Si. The measured valence band offset value between Ta2O5 and the Si substrate was 3.08 eV after 2.5 cycles.

• 한국재료학회지
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• 제3권3호
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• pp.292-299
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• 1993

본 연구에서는 탄소/탄소복합재료의 마모특성에 대한 탄소섬유 길이의 영향을 고찰하였다. 매트릭스 precursor로 레졸형의 페놀수지와 강화재로 표면처리를 하지않은 PAN계 단섬유형 탄소섬유를 사용하여 액상함침법으로 1회의 고온열처리 공정과 4회의 탄화공정을 통하여 탄소/탄소복합재료를 제조하였다. Disk-on-disk형의 마모시험기를 통하여 상대 마찰재로 AISI 304 stainliss steel을 사용하여 0.6MPa(61 ${\times}{10^3}$Kg/$m^2$)의 압력과 0.71m/sec의 미끄러짐 속도하에서 측정된 탄소/탄소복합재료의 마찰계수는 0.2-0.3이었다. 마찰계수에 대한 섬유의 길이의 영향은 크게 나타나지 않았지만, 마모 속도는 섬유의 길이가 증가함에 따라 증가하는 경향이 나타났다. 본 실헙 결과를 섬유 강화 플라스틱의 마모 모델을 적용하여 고찰하여 본 결과, 섬유의 길이가 증가함에 따라 탄소/탄소복합재료의 마모 속도가 증가되는 경향은 생성된느 마모조각의 크기가 커기기 때문에 나타난 현상으로 판단되었다.

• Toxicological Research
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• 제28권4호
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• pp.235-240
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• 2012

$^{99m}Tc$ tricarbonyl glycine monomers, trimers, and pentamers were synthesized and evaluated for their radiolabeling and in vivo distribution characteristics. We synthesized a $^{99m}Tc$-tricarbonyl precursor with a low oxidation state (I). $^{99m}Tc(CO)_3(H_2O)_3^+$ was then made to react with monomeric and oligomeric glycine for the development of bifunctional chelating sequences for biomolecules. Labeling yields of $^{99m}Tc$-tricarbonyl glycine monomers and oligomers were checked by high-performance liquid chromatography. The labeling yields of $^{99m}Tc$-tricarbonyl glycine and glycine oligomers were more than 95%. We evaluated the characteristics of $^{99m}Tc$-tricarbonyl glycine oligomers by carrying out a lipophilicity test and an imaging study. The octanol-water partition coefficient of $^{99m}Tc$ tricarbonyl glycine oligomers indicated hydrophilic properties. Single-photon emission computed tomography imaging of $^{99m}Tc$-tricarbonyl glycine oligomers showed rapid renal excretion through the kidneys with a low uptake in the liver, especially of $^{99m}Tc$ tricarbonyl triglycine. Furthermore, we verified that the addition of triglycine to prototype biomolecules (AGRGDS and RRPYIL) results in the improvement of radiolabeling yield. From these results, we conclude that triglycine has good characteristics for use as a bifunctional chelating sequence for a $^{99m}Tc$-tricarbonyl-based biomolecular imaging probe.

• 한국초전도ㆍ저온공학회논문지
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• 제20권4호
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• pp.46-49
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• 2018

To improve in-field critical current densities ($J_c$) of $GdBa_2Cu_3O_{7-{\delta}}$ (GdBCO) coated conductors(CCs) fabricated by the reactive co-evaporation by deposition and reaction (RCE-DR) process, employing the nominal composition of Gd:Ba:Cu=1:1:2.5, we tried to refine the $Gd_2O_3$ particles trapped in the GdBCO superconducting matrix. For this purpose, we carefully selected the processing conditions on the stability phase diagram of GdBCO for this composition. By lowering the growth temperature of $Gd_2O_3$ in the liquid, we could refine the average particle size of $Gd_2O_3$ particles trapped in the GdBCO matrix and also achieve the zero-resistive transition temperatures ($T_{c,zero}$) of 92.3~94.2 K. Unfortunately, however, it was unsuccessful to achieve enhanced in-field $J_c$ values from these samples because of an air-contamination of the amorphous precursor film before its conversion into crystalline GdBCO film, suggesting that any exposure of the amorphous precursor film to air is fatal in obtaining high performance GdBCO CCs via the RCE-DR process.

• Journal of Pharmaceutical Investigation
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• 제39권1호
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• pp.73-78
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• 2009

A simple LC-MS/MS method of rabeprazole in human plasma was developed and validated. Rabeprazole and Internal standard (I.S), omeprazole, were extracted from human plasma by liquid liquid extraction, chromatographic separation of rabaprazole in plasma was achieved at $45^{\circ}C$ with a Shiseido UG120 $C_{18}$ column and methanol-10 mM ammonium acetate buffer (pH 9.42 with ammonium water), as mobile phase. Rabeprazole produced a protonated precursor ion [$(M+H)^+$] at m/z 360.10 and corresponding product ion at m/z 242.21. Internal standard produced a protonated precursor ion [$(M+H)^+$] at 346.09 and corresponding product ion at m/z 198.09. This method showed linear response over the concentration range of $1{\sim}500\;ng/mL$ with correalation coefficient greater than 0.99. The lower limit of quantitation (LLOQ) using 0.2 mL plasma was 1 ng/mL, which was sensitive enough for pharmacokinetics studies. The method was specific and validated with a limit of quantitation of 1 ng/mL. The intra-day and inter-day precision and accuracy were acceptable for all samples including the LLOQ. The applicability of the method was demonstrated by analysis of plasma after administration of a single 10 mg dose to 36 healthy subject. From the plasma rabeprazole concentration versus time curves, the mean $AUC_t$ (The area under the plasma concentration-time curve from time 0 to 12 hr ) was $691.36{\pm}321.88\;ng{\cdot}hr/mL$, $C_{max}$ (maximum plasma drug concentration) of $353.21{\pm}131.52\;ng/mL$ reached $3.4{\pm}1.1\;hr$ after adiministration. The mean biological half-life of rabeprazole was $1.37{\pm}0.75\;hr$. Based on the results, this simple method could readily be used in pharmacokinetics studies.

• Journal of Pharmaceutical Investigation
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• 제37권4호
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• pp.223-227
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• 2007

A rapid, simple and sensitive LC/MS/MS method for the determination of lercanidipine in human serum was validated and applied to the pharmacokinetic study of lercanidipine. Lercanidipine and internal standard, amlodipine, were extracted from human serum by liquid-liquid extraction with hexan-isoamyl alcohol (100: 1, v/v) and analyzed on a $Symmetry^{(R)}$ MS $C_{18}$ column with the mobile phase of acetonitrile-0.2% aqueous formic acid (70: 30, v/v). Using MS/MS with multiple reaction monitoring (MRM) mode, lercanidipine and amlodipine were detected without severe interferences from human serum matrix. Lercanidipine produced a protonated precursor ion ($[M+H]^+$) at m/z 612.3 and a corresponding product ion at m/z 280.0. Internal standard produced a protonated precursor ion ($[M+H]^+$]) at m/z 409.0 and a corresponding product ion at m/z 238.0. The ruggedness of this method was investigated using quality control (QC) samples. This method showed linear response over the concentration range of 0.05-20 ng/mL with correlation coefficient greater than 0.999. The lower limit of quantitation using 0.5 mL of serum was 0.05 ng/mL, which was sensitive enough for pharmacokinetic studies. The overall accuracy of the developed method ranged from 85.51 to 112.2% for lercanidipine with overall precision (% C.V.) being 3.56-13.1%. This method showed good ruggedness (within 15% C.V.) and was successfully applied for the analysis of lercanidipine in human serum samples for the pharmacokinetic studies, demonstrating the suitability of the method.

• 전기화학회지
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• 제13권2호
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• pp.145-152
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• 2010

본 연구에서는 organophosphate를 기반으로 한 과불소화된 아크릴레이트 가교제를 사용하여 제조한겔 고분자 전해질의 이온 전도도 및 전기화학적 특성을 평가하였다. 과불소화된 아크릴레이트 가교제를 사용하여 만든 겔 고분자 전해질은 액체전해질의 함량이 최대 97 wt%까지 안정한 겔 상태를 유지하였다. 본 연구에서 제조한 겔 고분자 전해질의 이온전도도는 $30^{\circ}C$에서 $1.0\;{\times}\;10^{-2}\;S/cm$의 값을 가졌다. 또한 전기화학적 안정성 테스트에서도 약 4.5V로 이상까지 산화에 의한 열화가 없이 안정하였다. 합성된 겔고분자 전해질을 리튬이온 고분자 전지에 적용하여 그 활용성을 평가하였다. 양극으로는 $LiCoO_2$를 사용하였으며 음극으로는 카본을 사용하였다. 이렇게 만든 리튬이온 고분자 전지는 0.1C에서 136.11 mAh/g의 용량으로 이론용량과 거의 비슷한 값을 나타내었으며, 2C 방전에서도 초기 용량의 91%를 유지하였다. 또한 500번의 충방전 후에도 초기 용량의 70%정도의 용량을 유지하였다.

• Korean Chemical Engineering Research
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• 제43권5호
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• pp.609-615
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• 2005

$1{\mu}l$ 정도의 미량 titanium tetraisopropoxide(TTIP)를 주사기를 사용하여 1 cc 부피의 증발관에 주입하여 기화시킨 후 질소에 의해 직경 4 mm, 길이 35 cm의 관형 에어로졸반응기로 운반하여 열분해 시킴으로써 30-300 nm 크기의 $TiO_2$ 나노입자를 제조하였으며, 반응온도 및 TTIP 증기 농도가 생성된 $TiO_2$ 입자의 형상, 크기, 결정성 등에 미치는 영향을 조사하였다. 전구체 증기 농도 1 mol%에서 반응온도를 300, 500, $700^{\circ}C$로 변화시킨 결과 반응온도가 증가함에 따라 응집체를 구성하고 있는 1차 입자 크기가 감소하였고, $700^{\circ}C$에서는 입자 크기분포가 bimodal 형태를 나타내었다. 반응온도를 $700^{\circ}C$로 유지하고 전구체 증기 농도를 1, 3.5, 7 mol%로 변화시킨 결과 전구체 증기 농도 3.5 mol% 이상에서는 1 mol%에서 관찰되었던 bimodal 분포가 사라지고 응집체 내 1차 입자들의 개수가 상대적으로 많이 증가하였다. 반응온도 및 전구체 농도가 입자의 형상, 크기분포에 미치는 이와 같은 영향들을 이전의 연구결과들과 함께 비교 분석하였다.