• 제목/요약/키워드: Synthesis condition

검색결과 912건 처리시간 0.024초

Alum Catalyzed Simple and Efficient Synthesis of Bis(indolyl)methanes by Ultrasound Approach

  • Sonar, Swapnil S.;Sadaphal, Sandip A.;Kategaonkar, Amol H.;Pokalwar, Rajkumar U.;Shingate, Bapurao B.;Shingare, Murlidhar S.
    • Bulletin of the Korean Chemical Society
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    • 제30권4호
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    • pp.825-828
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    • 2009
  • Alum $(KAl(SO_4)_2{\cdot}12H_2O)$ is an inexpensive, efficient, non‐toxic and mild catalyst for the synthesis of bis(indolyl)methanes by the reaction of 1H-indole with various aldehydes/ketones under the influence of ultrasound irradiation in solvent‐free condition. The remarkable advantages of this method are the simple experimental procedures, shorter reaction times, high yields of product and green aspects by avoiding toxic catalysts and solvents.

Immobilization of L-Lysine on Zeolite 4A as an Organic-Inorganic Composite Basic Catalyst for Synthesis of α,β-Unsaturated Carbonyl Compounds under Mild Conditions

  • Zamani, Farzad;Rezapour, Mehdi;Kianpour, Sahar
    • Bulletin of the Korean Chemical Society
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    • 제34권8호
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    • pp.2367-2374
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    • 2013
  • Lysine (Lys) immobilized on zeolite 4A was prepared by a simple adsorption method. The physical and chemical properties of Lys/zeolite 4A were investigated by X-ray diffraction (XRD), FT-IR, Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and UV-vis. The obtained organic-inorganic composite was effectively employed as a heterogeneous basic catalyst for synthesis of ${\alpha},{\beta}$-unsaturated carbonyl compounds. No by-product formation, high yields, short reaction times, mild reaction conditions, operational simplicity with reusability of the catalyst are the salient features of the present catalyst.

Design and Synthesis of Chromenone derivatives as Potential Antioxidants

  • Kang, Hae-Eun;Lee, Kum-Ho;Lee, Dae-Hee;Cho , Jung-Sook;Lee, Hee-Soon
    • 대한약학회:학술대회논문집
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    • 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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    • pp.351.3-353
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    • 2002
  • Oxygen radicals are produced in many pathophysiologic states whether the event is a causal factor of illness or is a result of their progression. Oxygen radicals including superoxide anions. hydrogen peroxide are thought to be involved in a number of type of acute. and chronic pathologic condition in the brain and neural tissue. So the antioxidants have recently received much attention as therapeutic agent for the treatment of neurodegenerative disease. In this study. we describe synthesis of a series of chromenone derivatives as antioxidant agents. The target compounds are designed to include the structural frature of caffeic acid. flavoniod. and focopherol known as antioxidants.

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초음파 조건에서 산화제를 이용한 풀러렌 산화물의 제조 (Preparation of Fullerene Oxides by Fullerenes[$C_{60},C_{70}$] with Several Oxidants under Ultrasonic Condition)

  • 권석찬;정홍석;고원배
    • Elastomers and Composites
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    • 제38권2호
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    • pp.147-156
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    • 2003
  • 풀러렌[$C_{60},\;C_{70}$]을 benzoylperoxide, trichloroisocyanuric acid, methyltrioxorhenium(VII), iodosobenzene 그리고 phosphorous pentoxide 등의 산화제를 사용하여 상온, 초음파 조건에서 풀러렌 산화물을 제조하였다. MALDI-TOF MS, UV-VIS 그리고 HPLC를 사용하여 분석한 결과 생성된 풀러렌 산화물은 [$C_{60}(O)_n$], ($n=1{\sim}3$ 또는 n=1)과 [$C_{70}(O)_n$], ($n=1{\sim}2$ 또는 n=1)임을 알 수 있었다. 한편, 동일한 실험 조건에서 $C_{60}$ 반응속도는 $C_{70}$ 보다 높았다.

고에너지 밀링 및 합성반응에 의한 Fe-TiC 복합분말 제조 (Fabrication of Fe-TiC Composite Powder by High-Energy Milling and Subsequent Reaction Synthesis)

  • 안기봉;이병훈;이용희;;김지순
    • 한국분말재료학회지
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    • 제20권1호
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    • pp.53-59
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    • 2013
  • Fe-TiC composite powder was fabricated via two steps. The first step was a high-energy milling of FeO and carbon powders followed by heat treatment for reduction to obtain a (Fe+C) powder mixture. The optimal condition for high-energy milling was 500 rpm for 1h, which had been determined by a series of preliminary experiment. Reduction heat-treatment was carried out at $900^{\circ}C$ for 1h in flowing argon gas atmosphere. Reduced powder mixture was investigated by X-ray Diffraction (XRD), Field Emission-Scanning Electron Microscopy (FE-SEM) and Laser Particle Size Analyser (LPSA). The second step was a high-energy milling of (Fe+C) powder mixture and additional $TiH_2$ powder, and subsequent in-situ synthesis of TiC particulate in Fe matrix through a reaction of carbon and Ti. High-energy milling was carried out at 500 rpm for 1 h. Heat treatment for reaction synthesis was carried out at $1000{\sim}1200^{\circ}C$ for 1 h in flowing argon gas atmosphere. X-ray diffraction (XRD) results of the fabricated Fe-TiC composite powder showed that only TiC and Fe phases exist. Results from FE-SEM observation and Energy-Dispersive X-ray Spectros-copy (EDS) revealed that TiC phase exists uniformly dispersed in the Fe matrix in a form of particulate with a size of submicron.

자체반응열 고온합성법을 이용한 Titanium Carbonitride의 합성에 관한 연구 (A Study on the Synthesis of Titanium Carbonitride by SHS(Self-propagating High-temperature Synthesis) Method)

  • 하호;황규민;이희철
    • 한국세라믹학회지
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    • 제31권6호
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    • pp.637-642
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    • 1994
  • Using SHS(Self-propagating High-temperature Synthesis) method, the optimum synthetic condition of titanium carbonitride was established by controlling the parameters such as relative density of mixture (Ti+C), nitrogen pressure, additive amounts of titanium hydride(TiH1.924) and protecting heat loss. Under 1 atm nitrogen pressure, nitridation ratio with changing relative density of the sample compacts has a maximum (87.2%) at about 55%, and in the case of enveloping the pellet with a quartz tube, the highest nitridation ratio of 90% was obtained at about 68%. At relative density of 55%, nitridation ratio with the nitrogen pressure has a miximum (87.3%) at 7 atm. As the amounts of additive titanium hydride increased, nitridation ratio decreased at below 7 atm nitrogen pressure and, increased at above this pressure until percent of addition percent reached 15 wt% and decreased abruptly upon futher increases in titanium hydride. In the synthesis of TiCxNy by combustion reaction, heat transfer from combustion zone to preheating zone and nitrogen gas penetration into the compact were found to be important factors affecting the TiCxNy formation. It was difficult to obtain high nitridation ratio when the conbustion temperature was either too high or too low, and it seems that the retention of high temperature after a combustion wave sweeped through the reactant mixture pellet is critical to obtain a satisfactory nitridation ratio.

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역미셀을 이용한 감마-알루미나 나노입자 합성에 대한 통계적 분석 (Statistical Analysis of Synthesis of Gamma-alumina (γ-Al2O3) Nanoparticles Using Reverse Micelles)

  • 이길우;유계상
    • 공업화학
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    • 제28권3호
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    • pp.351-354
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    • 2017
  • 역미셀법을 이용하여 열적 안정성이 우수한 감마-알루미나의 합성 공정을 최적화하기 위하여 실험계획법을 사용하였다. 먼저 합성공정에 주 요소인 계면활성제, 물 및 오일의 비에 대한 최적의 실험조건을 설계하기 위하여 혼합물 실험법을 이용하여 12가지 실험조건을 도출하였다. 설계된 조건에서 역미셀법을 이용하여 합성한 입자를 $900^{\circ}C$에서 소성한 결과 입자의 크기에 차이는 있었지만 모두 감마-알루미나 결정구조를 가졌다. 도출된 실험결과를 이용하여 계산된 2차 회귀모델의 결정계수는 93.68%이었으며, P- 값이 0.002로서 유의하다고 할 수 있다. 다양한 입자크기를 가지는 감마-알루미나의 합성조건을 모든 범위에서 대하여 표면도와 등고선도를 이용하여 제시하였다. 그 결과 Surfactant/Water/Oil의 질량비가 0.3450/0.0729/0.5821인 조건에서 합성할 때 약 2.8 nm의 가장 작은 입자가 합성되는 것으로 계산되었다.

반응 표면 분석법을 이용한 일체형 흡착제의 합성 조건 최적화 (Optimization of Synthesis Condition of Monolithic Sorbent Using Response Surface Methodology)

  • 박하은;노경호
    • 공업화학
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    • 제24권3호
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    • pp.299-304
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    • 2013
  • Box-Behnken design (BBD) 방법은 일체형 흡착제의 합성조건을 최적화하기 위해 사용되었다. 단량체(monomer)의 양(mL), 가교제(crosslink)의 양(mL), porogen의 양(mL)에 대한 효과를 조사했다. 실험 값은 여러 회귀분석 및 통계적인 방법에 의해 2차 다항 방정식을 얻었다. 이 모델의 결정계수($R^2$)는 0.9915이고 결정계수의 p value는 0.0001보다 작은 값으로 모델이 매우 유의미하다는 것을 나타낸다. RSM 모델에 의해 예측된 최적의 일체형 흡착제 합성조건은 단량체의 양 0.30 mL, 가교제의 양 1.40 mL, porogen의 양 1.47 mL이고 이 조건 아래서 합성된 일체형 흡착제의 양은 2120.15 mg이다. 이 결과는 이 모델이 적절하다는 것을 나타내었다.

Controllable Biogenic Synthesis of Intracellular Silver/Silver Chloride Nanoparticles by Meyerozyma guilliermondii KX008616

  • Alamri, Saad A.M.;Hashem, Mohamed;Nafady, Nivien A.;Sayed, Mahmoud A.;Alshehri, Ali M.;El-Shaboury, Gamal A.
    • Journal of Microbiology and Biotechnology
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    • 제28권6호
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    • pp.917-930
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    • 2018
  • Intracellular synthesis of silver/silver chloride nanoparticles (Ag/AgCl-NPs) using Meyerozyma guilliermondii KX008616 is reported under aerobic and anaerobic conditions for the first time. The biogenic synthesis of Ag-NP types has been proposed as an easy and cost-effective alternative for various biomedical applications. The interaction of nanoparticles with ethanol production was mentioned. The purified biogenic Ag/AgCl-nanoparticles were characterized by different spectroscopic and microscopic approaches. The purified nanoparticles exhibited a surface plasmon resonance band at 419 and 415 nm, confirming the formation of Ag/AgCl-NPs under aerobic and anaerobic conditions, respectively. The planes of the cubic crystalline phase of the Ag/AgCl-NPs were confirmed by X-ray diffraction. Fourier-transform infrared spectra showed the interactions between the yeast cell constituents and silver ions to form the biogenic Ag/AgCl-NPs. The intracellular Ag/AgCl-NPs synthesized under aerobic condition were homogenous and spherical in shape, with an approximate particle size of 2.5-30nm as denoted by the transmission electron microscopy (TEM). The reaction mixture was optimized by varying reaction parameters, including temperature and pH. Analysis of ultrathin sections of yeast cells by TEM indicated that the biogenic nanoparticles were formed as clusters, known as nanoaggregates, in the cytoplasm or in the inner and outer regions of the cell wall. The study recommends using the biomass of yeast that is used in industrial or fermentation purposes to produce Ag/AgCl-NPs as associated by-products to maximize benefit and to reduce the production cost.

규산알루민산마그네슘의 합성조건과 유동학적 특성 (Synthesis Conditions and Rheological Characteristics of Aluminum Magnesium Silicate)

  • 신화우;정동훈
    • 약학회지
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    • 제39권1호
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    • pp.68-77
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    • 1995
  • Aluminum magnesium silicate was synthesized by reacting the mixed solutions of sodium aluminate and magnesium chloride with sodium silicate solution in this study. The optimal synthesis conditions based on the yield of the product has been attained according to Box-Wilson experimental design. It was found that the optimal synthetic conditions of aluminum magnesium silicate were as follows: Reaction temperature=$69~81^{\circ}C$; concentration of two reactants, sodium aluminate and magnesium chloride= 13.95~14.44 w/w%; molar concentration ratio of the two reactants, [NaAlO$_{2}$]/MgCl$_{2}$]=3.63~4.00; reaction time= 12~15 min; drying temp. of the product=$70~76^{\circ}C$. Aluminum magnesium silicate synthesized under the optimal synthesis condition was dispersed in 0.75, 1.0 and 1.5w/w% aqueous solution or suspension of six dispersing agents, and the Theological properties of the dispersed systems prepared have been investigated at $15^{\circ}C$ and $25^{\circ}C$ using Brookfield LVT Type Viscometer. The acid-consuming capacity of the most excellent product was 272~278 ml of 0.1N-HCl per gram of the antacid. The flow types of 5.0 w/w% aluminum magnesium silicate suspension were dependent upon the kind and concentration of dispersing agents added. The apparent viscosity of the suspension was generally increased with concentration of dispersing agents and was not significantly changed or decreased as the temperature was raised. A dispersing agent, hydroxypropyl cellulose suspension, exhibited an unique flow behavior of antithixotropy. The flow behavior of the suspension dispersed in a given dispersing agent not always coincided with that of the dispersing agent solution or suspension itself.

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