• 제목/요약/키워드: X-ray diffractometry

검색결과 307건 처리시간 0.026초

백금담지 활성탄소 촉매의 요오드화수소 분해 특성 연구 (A Study on the HI Decomposition by Carbon-Supported Platinum Catalyst)

  • 박정은;김정민;강경수;김창희;김영호;박주식;배기광
    • 한국수소및신에너지학회논문집
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    • 제17권3호
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    • pp.301-308
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    • 2006
  • The present work explores the effect of carbon-supported platinum catalyst on the HI decomposition using gas adsorption analyzer, thermogravimetry, X-ray diffractometry, scanning electron microscopy, and gas chromatography. For this purpose, three types of activated carbon (C), Pt/C-1 wt.%, and Pt/C-5 wt.% were prepared. The HI gas conversion is crucially influenced by the amount of Pt on the carbon support. The more the amount of Pt was, the higher results in the HI gas conversion. For three types of catalysts, HI conversion increased with increasing the decomposition temperature but with decreasing the space velocity. The increase of HI conversion with temperature was more pronounced in activated carbon than that in Pt/C. From EDX result, it was found that the activated carbon comprised higher amount of iodine than the Pt/C after the decomposition reaction. This implies that the HI conversion is closely related to the amount of Iodine.

리튬이차전지용 바나듐계 복합양극의 특성 (The Characteristics of Vanadium based Composite Cathode for Lithium Secondary Battery)

  • 김종진;손원근;김재용;박수길
    • 전기화학회지
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    • 제2권2호
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    • pp.61-65
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    • 1999
  • 리튬이차전지용 양극물질로서 $LiV_3O_8$의 새로운 합성방법이 그 전기화학적 거동을 향상시키는 것으로 제안되고 있다. $LiV_3O_8$을 수용성 lithium trivanadate 겔의 탈수에 의해 잘 분산된 형태로 얻어진다. $LiV_3O_8$의 초음파처리방법은 solutionmethod에 의해 만들어진 초기상태의 $LiV_3O_8$과 비교된다. 수용액상에서 초음파처리 된 물질은 XRD, TGA, SEM등으로 물리적특성을 확인하였다. 이런 방법들은 수용성 $LiV_3O_8$의 초음파처리공정이 결정성을 감소시키고 비표면적과 공간용량을 향상시키는 것으로 나타났다. 특히 2시간 동안 초음파처리한 것은 높은 방전용량을 가지며, 대용량의 손실없이 충방전사이클이 이루어졌다. 따라서, 초음파처리 된 $LiV_3O_8$은 공간용량을 향상시킬 뿐만 아니라 사이클거동 역시 향상되었다.

Isolation, Physicochemical Properties and Toxicities of Territrem A' and B'

  • Ling, Kuo Huang;Peng, Fu Chuo;Chen, Bai Jiun;Wang, Yu;Lee, Gene Hsiang
    • 생약학회지
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    • 제17권2호
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    • pp.153-160
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    • 1986
  • We have isolated two new metabolites of territrem, designated as territrem $A'\;(TRA';\;C_{28}H_{30}O_{10})$ and $B'\;(TRB';\; C_{29}H_{34}O_{10})$ from chloroform extract of rice culture of Aspergillus terreus 23-1, using the same isolation procedure as that for territrem A, B and C(TRA, TRB, TRC). The present isolation procedure gave about 5 mg of TRA' and 10 mg of TRB' from 4 kg of rice culture per batch. Analysis of the high resolution mass spectrum showed that the molecular composition of TRA' and TRB' are $C_{28}H_{30}O_{10}$ and $C_{29}H_{34}O_{10}$ respectively, Some results of physicochemical properties were presented in this paper. Single crystal X-ray diffractometry of TRB' showed that the three dimensional structure of TRB' has not changed significantly from that of $TRB\;(C_{29}H_{34}O_9)$, except for the insertion of one oxygen atom into TRB to make additional pyran in the E-ring. It is also suggested that the aromatic moiety of TRA' is similar to that of $TRA\;(C_{28}H_{30}O_9)$ and the rest non-aromatic portions resemble to those of TRB'. The tremorgenic activity, lethality and inhibitory effect on acetylcholine esterase of TRA' and TRB' are greatly reduced comparing to that of TRA and TRB.

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EFFECT OF DEPOSITION METHODS ON PHYSICAL PROPERTIES OF POLYCRYSTALLINE CdS

  • Lee, Y.H.;Cho, Y.A.;Kwon, Y.S.;Yeom, G.Y.;Shin, S.H.;Park, K.J.
    • 한국표면공학회지
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    • 제29권6호
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    • pp.862-868
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    • 1996
  • Cadmium sulfide is commonly used as the window material for thin film solar cells, and can be prepared by several techniques such as sputtering, spray pyrolysis, close spaced sublimation (CSS), thermal evaporation, solution growth methods, etc. In this study, CdS films were deposited by thermal evaporation, close spaced sublimation, and solution growth methods, respectively, and the effects of the methods on physical properties of polycrystalline CdS deposited on ITO/glass were investigated. Also, the effects of variously prepared CdS thin films on the physical properties of CdTe deposited on the CdS were investigated. The thickness of polycrystalline CdS films was maintained at $0.3\mu\textrm{m}$ except for the solution grown CdS when $0.2\mu\textrm{m}$ thick CdS was deposited. After the deposition, all the samples were annealed at $400^{\circ}C$ or $500^{\circ}C$ in H2 atmosphere. To investigate physical properties of the deposited and annealed CdS thin films, UV-VIS spectro-photometry, X-ray diffractometry (XRD), and Auger electron spectroscopy (AES), and cross sectional transmission electron microscopy(XTEM) were used to analyze grain size, crystal structure, preferred orientation, optical properties, etc. The annealed CdS showed the bandedge transition at 510nm and the optical transmittance high than 80% for all of the variously deposited films. XRD results showed that CdS thin films variously deposited and annealed had the same hexagonal structures, however, showed different preferred orientations. CSS grown CdS had [103] preferred orientation, thermally evaporated CdS had [002], and CdS grown by the solution growth had no preferred orientation. The largest grain size was obtained for the CSS grown CdS while the least grain size was obtained for the solution grown CdS. Some of the physical properties of CdTe deposited on the CdS thin film such as grain size at the junction and grain orientation were affected by the physical properties of CdS thin films.

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Pranoprofen Argininate 및 Pranoprofen Lysinate의 약제학적 연구 (Pharmaceutical Study on Pranoprofen Argininate and Pranoprofen Lysinate)

  • 지웅길
    • Journal of Pharmaceutical Investigation
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    • 제17권4호
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    • pp.197-204
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    • 1987
  • Novel pranoprofen algininate and lysinate salts were manufactured and their salt formation was confirmed by melting point, infrared spectroscopy, nuclear magnetic resornance spectroscopy, differential scanning calorimetry and powder X-ray diffractometry. The physical properties of pranoprofen lysinate and argininate salts were compared with those of pranoprofen through in vitro and in vivo tests. Solubility, $pK_a$ and lipid-water partition coefficient were measured through in vitro experiments, while antiinflammatory efficacy, analgesic effect, acute toxicity and in situ absorption were tested through in vivo experiments. The results obtained were as follows: 1) The solubilities of pranoprofen argininate and lysinate salts were increased markedly in pH 6.8 and pH 7.5 phosphate buffer solutions, comparing with that of pranoprofen itself. 2) $pK_a$ values of pranoprofen, pranoprofen argininate and lysinate salts were 6.34, 7.99 and 7.56 in carbon tetrachloride, and 5.86, 6.69 and 7.92 in chloroform, respectively by liquid-liquid partition method. 3) The lipid-water partition coefficients of pranoprofen argininate and lysinate salts were increased more than that of pranoprofen in carbon tetrachloride, chloroform, or benzene-pH 6.8 buffer system, but were nearly identical using pH 1.2 buffer as water phase. 4) Antiinflammatory effects of pranoprofen argininate and lysinate salts were remarkably increased and analgesic effects of the salts were as same as that of pranoprofen. 5) Pranoprofen argininate and lysinate salts were safer than pranoprofen itself in acute toxicity, and the in situ absorption rates of pranoprofen, pranoprofen argininate and lysinate salts were 0.392, 0.960 and $0.762\;hr^{-1}$, respectively according to the rat intestine recirculation experiment.

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이온교환수지를 이용한 새로운 암로디핀 복합체 개발 (Development of New Amlodipine Complex using Ion Exchange Resin)

  • 정상영;안기영;안건석;길영식;황성주
    • Journal of Pharmaceutical Investigation
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    • 제38권1호
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    • pp.9-14
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    • 2008
  • Cation exchange resin complex of amlodipine free base has been investigated to improve the stability and dissolution profile. The complex was prepared by reacting amlodipine solution with activated cation exchange resin, and amlodipine content in the complex was 31.6% calculated by HPLC determination. Its product was not physical mixture but the complex formed by ionic bond, which was identified by microscope system, differential scanning calorimetry and X-ray diffractometry. Each tablet containing amlodipine free base(I) and its complex(II) was prepared for the accelerated stability test ($40^{\circ}C$, 75%RH) and dissolution test in the pH 1.2 buffer solution and purified water media. Dissolution patterns of formulation II in both media were similar to those of $Norvasc^{(R)}$ tablet, but the pattern of formulation I in purified water was different. After 6 months storage under stability test, amlodipine content of formulation I, II and $Norvasc^{(R)}$ tablet were $99.3{\pm}1.2%,\;98.9{\pm}1.4%\;and\;83.9{\pm}3.4%$, respectively. While amlodipine free base was unstable at the condition, its complex was not only significantly stable, but also similar in the dissolution pattern. These results suggest the usefulness of complex as a stable carrier for amlodipine free base.

$B_t$ Band의 형성 과정 (Origin of Banded $B_t$ Horizons in Sandy Deposits)

  • 오경섭
    • 한국제4기학회지
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    • 제3권1호
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    • pp.35-45
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    • 1989
  • 한국과 서부 유럽의 사질층에 발달해 있는 $B_t$ band의 성인은 퇴적학적인 현상과는 무관하다. 그렇다고 토양학적인 사고만으로도 설명될 수 없다. 본 연구 결과 $B_t$ band는 사질층이 형성된 후 시기를 달리하여 다음과 같이 두 부류의 물질이 서로 다른 메카니즘에 의해 이동.집적되어 형성되었다. 1)먼저 silt중심의 heterometric fine grains과 운모류들이 결빙과 관련된 cryophoresis에 의해 이동되어 이들이 사질층 단면에서 밴드 형태로 집적되었고 2)다음에 철분을 함유한 점토가 토양수에 의해 이미 형성된 맨드에 집적되어 결국 적색의 $B_t$ band가 형성되었다. 이 두 과정에서 전자는 토양의 결빙이 지표에서 3m 정도 이상까지 진전될 정도로 한랭하고 습윤한 환경과, 후자는 podzolization이 진행되는 정도의 냉량.습윤한 환경과 관련된다. 오늘날 갈색토화작용(brunification)이 진전되는 우리나라와 서부 유럽의 경우, $B_t$ band의 polygenetic한 성인과 관련된 한랭.습윤한 환경들은 제4기 근자(주로 Wurm빙기 이래)의 고환경으로 추정된다.

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Trimethyl-indium 소스 고갈에 따른 InGaAsP 에피층의 특성 변화 (Effect of trimethyl-indium source depletion on InGaAsP epilayer grown by MOCVD)

  • 김현수;오대곤;편광의;최인훈
    • 한국진공학회지
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    • 제9권4호
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    • pp.400-405
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    • 2000
  • 유기금속 소스의 농도를 연속적으로 in-situ 측정이 가능한 EPISON ultrasonic monitor를 이용하여 TMIn(trimethly-indium)의 소스 고갈이 InGaAs, InGaAsP bulk 에피층과 1.55 $mu extrm{m}$ InGaAs/InGaAsP SMQW (strained multi-quantum well)에 미치는 영향을 조사하였다. TMIn 소스는 사용량이 80%에서 급격하게 소스 고갈 현상을 보였다. TMIn 소스는 사용량이 80%에서 급격하게 소스 고갈 현상을 보였다. TMIn 소스 고갈에 의한 에피층의 특성 변화를 조사한 결과, bulk 에피층의 경우에는 소스가 고갈 되기 전에 성장한 에피층과 비교하여 DCXRD(double crystal X-ray diffractometry) spectrum에서 피크 분리가 약 300 arcsec정도 Ga-rich 방향으로 이동하였으며 relative FWHM은 약 2배 가량 증가하는 것을 보였다. SMQW 구조에서는 bulk 에피층과는 달리, PL 중심파장에서도 약 40 nm 정도 단파장쪽으로 이동하였으며, 피크 분리는 약 300 arcsec정도 Ga-rich 방향으로 이동하였다. 하지만, EPISON의 closed loop 기능을 사용할 경우에는 TMIn 소스 사용량이 95%에서도 피크 분리가 $\pm$100 arcsec이내의 재현성 있는 에피층 성장이 가능하다는 것을 알 수 있었다.

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${\beta}$-시클로덱스트린과의 포접에의한 디플로페낙나트륨의 용해도 및 생체흡수율 증가 (Solubility and In vivo Absorption Enhancement of Diclofenac Sodium by ${\beta}-Cyclodextrin$ Complexation)

  • 이경태;김종환;김주일;김승조;서희경;서성훈
    • Journal of Pharmaceutical Investigation
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    • 제26권3호
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    • pp.169-174
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    • 1996
  • Inclusion complexes of diclofenac sodium with ${\beta}-cyclodextrin$ were prepared in aqueous solution, alkaline solution and solid phase. The interaction of diclofenac sodium with ${\beta}-cyclodextrin$ in pH 9.0 alkaline solution was evaluated by the solubility method and the instrumental analysis such as thermal analysis, infrared spectroscopy, X-ray diffractometry. The solubility of diclofenac sodium was increased linearly with the increase in the concentration of ${\beta}-cyclodextrin$up to 0.15 mol and showed that the aqueous solubility rate of diclofenac sodium was significantly increased by complex with ${\beta}-cyclodextrin$. The optimum composition of this complex was one molecule of ${\beta}-cyclodextrin$ included 1.59 molecular weight of diclofenac sodium as a guest molecule. The pharmacokinetic parameters of the diclofenac sodium and the complex with ${\beta}-cyclodextrin$ were studied in rats by oral route. $T_{max}$ between drug alone and inclusion complex showed significant difference to be 120 minute and 20 minute respectively. Both of $C_{max}$ and AUC of inclusion complex was about 40% higher than drug alone. It is estimated from the data in this study that complexation of diclofenac sodium with ${\beta}-cyclodextrin$ increased the absorption rate and improved the bioavalability of the diclofenac sodium by the formation of a water-soluble complexes.

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Effects of Bilayer Period on the Microhardness and Its Strengthening Mechanism of CrN/AlN Superlattice Coatings

  • Kim, SungMin;Kim, EunYoung;Kim, DongJun;La, JoungHyun;Lee, SangYul
    • 한국표면공학회지
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    • 제45권6호
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    • pp.257-263
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    • 2012
  • CrN/AlN multilayer coatings with various bilayer periods in the range of 1.8 to 7.4 nm were synthesized using a closed-field unbalanced magnetron sputtering method. Their crystalline structure, chemical compositions and mechanical properties have been investigated with Auger electron spectroscopy, X-ray diffractometry, atomic force microscopy, nanoindentation, scratch tests. The properties of the multilayer coatings varied strongly depending upon the magnitude of the bilayer period. The multilayer coating with a bilayer period of 1.8 nm showed the maximum hardness and an elastic modulus of approximately 37.6 and 417 GPa, respectively, which was 1.54 times higher than the hardness predicted by the rule of mixture from the CrN and AlN coatings. The hardness of the multilayer coating increased as the bilayer period decreased, i.e. as the rotation speed increased. The Hall-Petch type relationship, hardness being related to (1/periodicity)$^{-1/2}$, suggested by Lehoczky was confirmed for the CrN/AlN multilayer coatings with bilayer period close to the 5-10 nm range. With decreasing bilayer period, the surface morphology of the films became rougher and the critical load of films for adhesion strength gradually decreased.