• Title/Summary/Keyword: tin catalyst

검색결과 34건 처리시간 0.037초

금속염화물을 첨가한 루이스산 이온성 액체 촉매를 이용한 대두유로부터 바이오디젤 합성 (Synthesis of Biodiesel from Soybean Oil Using Lewis Acidic Ionic Liquids Containing Metal Chloride Salts)

  • 최재형;박용범;이석희;천재기;최재욱;우희철
    • Korean Chemical Engineering Research
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    • 제48권5호
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    • pp.643-648
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    • 2010
  • 본 연구에서는 이온성 액체인 염화콜린에 5가지의 금속염화물을 첨가하여 루이스산 이온성 액체 촉매를 제조하고, 이 촉매를 사용하여 대두유로부터 바이오디젤을 합성하였다. 먼저 단독의 금속염화물인 염화주석과 염화아연, 염화알루미늄, 염화철(III), 염화구리(I) 촉매에 대하여 363~423 K 온도 범위에서 에스터 교환 반응의 반응성을 조사하였다. 5가지의 금속염화물 중 염화주석이 우수한 촉매 활성을 나타내었고, 이러한 경향과 같이 5가지의 루이스산 이온성 액체 촉매 중 $[Me_3NC_2H_4OH]Cl-2SnCl_2$의 촉매가 403 K에서 14시간 동안 유지:메탄올:촉매의 몰 비율 1:12:0.9인 조건으로 최대 91.1%의 높은 반응수율을 나타내었다. 단독의 염화주석 촉매와는 달리, $[Me_3NC_2H_4OH]Cl-2SnCl_2$의 촉매는 반응 후 액체-액체 이상계를 형성하여 반응물과 생성물로부터 쉽게 분리할 수 있으며, 5회 이상 재사용 후에도 활성이 거의 감소하지 않았다. 이러한 결과는 촉매의 수분에 대해 안정성과 강한 루이스 산성도의 특성에 기인한 것으로 생각된다. 또한 촉매에 대한 반응시간과 촉매 및 메탄올 몰 비율 등의 반응변수들에 대한 영향이 조사되었다.

무전해 주석도금시의 문제점과 그 대책에 대한 연구 (Study on tin immersion plating on printed circuit boads)

  • 김동필;염희택
    • 한국표면공학회:학술대회논문집
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    • 한국표면공학회 2001년도 추계학술발표회 초록집
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    • pp.3-3
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    • 2001
  • Two companies plating baths were selected for plating on phenol and epoxy resin boards as well as on flexible p polyimide boards. After plating, deposited i&IIk&.ness al1d physical properties, as well as solder wettabilities by aging with $150^{\circ}C$ heating and 100% humidity were compared. After plating and aged with two different tin baths, deposited thickness and physical properties were not so great differences, but solder wettabilities were superior used polymer catalyst than the other. Furthermore depend upon the compactness and fineness of metallic sturctures of the base copper, the amounts of the plated copper were big differel1lces. These differences seems to be inherited from the kind and amount of additives. as well as current densities, which are influences upon structures of Copper layers. Generally the tin thickness are hetween 0.5 to $1.0\mu\textrm{m}$ and thicker the solder wettabilities are the better, and also me compact structures of deposits showed gooo soidierabiiities. In this study, with our own deveiotaedl plating equipment could get more than $0.5\mu\textrm{m}$ of till thickness and piating speed was $0.1\mu\textrm{m}$ per minutes.

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Synthesis and Characteristic of Polyurethane Modified Silicone

  • Lee, Kangseok;Shim, Sang Eun
    • Elastomers and Composites
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    • 제50권3호
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    • pp.210-216
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    • 2015
  • Polyurethane modified silicone (PUMS) was synthesized from various molecular weights of polydimethylsiloxane (PDMS 2000, PDMS 6000, PDMS 20000), polypropyleneglycol with molecular weight of 3000 g/mol (PPG 3000) and 2,4-toluenediisocyanate (TDI) under tin catalyst. Their structures were confirmed by the measurement of FT-IR and $^1H-NMR$, and the thermal properties were studied from DSC and TGA. Glass transition temperature of PUMS exhibited exothermic peak at $-63{\sim}-69^{\circ}C$, and residual weight was 19~35% at $800^{\circ}C$.

Methylchlorosilanes 합성촉매에 관한 연구 (A New Catalytic System for Methylchlorosilanes(MCS) Synthesis)

  • 조철군;한기도
    • 공업화학
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    • 제8권5호
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    • pp.804-810
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    • 1997
  • 실리콘의 모노머로 사용되고 있는 MCS 합성촉매계에 관한 연구를 수행하였다. 기존 3원촉매계(Cu/Zn/Sn)에 조촉매 Cd를 추가시킨 4원촉매계(CuCl/$ZnCl_2$/Sn/Cd)는 원료 규소와 염화메틸로부터 MCS를 합성하는 촉매로서 성능이 3원촉매계 보다 우수하였다. 4원촉매계는 조성이 혼합촉매/규소=5/95, Zn/Cu=0.1, Sn/Cu=0.001, Cd/Cu=0.001가 되도록 구성하고, 슬러리상태에서 혼합한 후 활성화된 접촉물질을 제조하여 MCS 합성에 사용하였을 때, 규소소모율 92%에서 평균선택도 92%, 규소소모율 40%에서 반응속도는 175(g-MCS/hr.kg-Si)이었다.

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Synthesis of High Molecular Weight 3-Arm Star PMMA by ARGET ATRP

  • Jeon, Hyun-Jeong;Youk, Ji-Ho;Ahn, Sung-Hee;Choi, Jin-Hwan;Cho, Kwang-Soo
    • Macromolecular Research
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    • 제17권4호
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    • pp.240-244
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    • 2009
  • High molecular weight(MW), 3-arm star poly(methyl methacrylate)(PMMA) with a narrow MW distribution($M_n$=570,000 g/mol, PDI=1.36) was successfully synthesized by activators regenerated by electron transfer(ARGET) atom transfer radical polymerization(ATRP). The polymerization was carried out with a trifunctional initiator/$CuBr_2$/N,N,N',N",N"-pentamethyldiethy lenetriamine(PMDETA) initiator/catalyst system in the presence of a tin(II) 2-ethylhexanoate [$Sn(EH)_2$] reducing agent at $90^{\circ}C$. The concentration of the copper catalyst was as low as 30 ppm, and a high initiation efficiency of the initiating sites was obtained. The chain-end functionality of the high MW, 3-arm star PMMA was confirmed by a chain extension experiment with styrene via ARGET ATRP, using the same catalyst system.

Copolymerization of L-Lactide and ${\varepsilon}$-Caprolactone in Supercritical Fluid

  • Prabowo, Benedictus;Choi, Dong-Hoon;Kim, Soo-Hyun
    • Macromolecular Research
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    • 제17권8호
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    • pp.575-579
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    • 2009
  • Copolymerization of L-lactide and s-caprolactone initiated by tin (II) octoate (Sn(Oct)$_2$) was carried out in supercritical chlorodifluoromethane (R22) with varying reaction conditions (time and temperature) and amounts of monomer and catalyst, under a pressure of 250 bar. The optimum conditions were a reaction time of 10 h and a temperature of 130 $^{\circ}C$, which is similar to the temperature used in bulk copolymerization system. The conversion increased from 56% to 76% by increasing the reaction time from 1 to 10 h. The molecular weight also increased to 75,900 g.mol$^{-1}$ over the same period, while the increased monomer concentration resulted in a high molecular weight of 86,400 g.mol$^{-1}$ and a monomer conversion of 84%. Raising the reaction temperature from 90 to 130 $^{\circ}C$ increased the monomer conversion as well as the poly-L-lactide-co-${\varepsilon}$-caprolactone (PLCL) molecular weight. The variation on the stannous octoate catalyst suggested that less catalyst would decrease the caprolactone content of the polymer.

Malic acid 함유 공중합체의 합성 및 필름표면의 RGD 고정화 (RGD Fixation of Film Surface and Synthesis of Copolymer Comprising Malic acid)

  • 이찬우;송경헌
    • 폴리머
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    • 제26권3호
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    • pp.300-306
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    • 2002
  • 본 연구에서는 세포접착성에 관한 영향을 검토하기 위하여 L-malic acid (L-MA)와 glycolic acid (GA)의 복합단위로 된 3-(S)-[(dodecyloxycarbonyl)methyl] -1,4-dioxane-2,5-dione (DMD)의 합성 및 DMD와 L-lactide의 공중합을 촉매로서 tin (II) octanoate를 사용하여 행하였다. 얻어진 공중합체를 필름으로 제작하여 RGD고정화를 실시한 결과, 필름표면에 세포접착성 펩티드를 고정화할 수 있었고, MA단위의 도입량의 증가에 따라 RGD의 고정화량이 증가하는 것을 확인하였으며, glycolic acid-$\beta$-dodecylmalate-lactic acid (D-PGML)는 서서히 분해되어 장기간에 있어 잔류 및 축적이 발생하지 않아 생체재료로서 크게 기대된다.

졸겔 연소법에 의한 nano crystalline ITO제작 및 특성 (Synthesis of nano porous indium tin oxide by sol-gel combustion hybrid method)

  • 정기영;곽동주;성열문;박차수
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 2009년도 제40회 하계학술대회
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    • pp.1328_1329
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    • 2009
  • Nano porous indium tin oxide (ITO) powder was synthesized employing a new route sol-gel combustion hybrid method using Ketjen Black as a fuel. The nano porous ITO powder was composed of $SnCl_4$-98.0% and $In(NO_3)_3{\cdot}XH_2O$-99.999%, produce with a $NH_4OH$ with sol-gel method as a catalyst [1,2]. Crystal structures were examined by powder X-ray diffraction (XRD), and those results show shaper intensity peak at $25.6^{\circ}(2{\Theta})$ of $SnO_2$ by increased sintering temperature. A particle morphology as well as crystal size was investigated by scanning electron microscopy(FE-SEM), and the size of the nano porous powder was found to be in the range of 20~30nm. ITO films could controlled by nano porous powder at various sintering temperature in this paper[3,4]. The sol-gel combustion method was offered simple and effective route for the synthesis of nano porous ITO powder[5].

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Pd-doped $SnO_2$-based oxide semiconductor thick-film gas sensors prepared by three different catalyst-addition processes

  • Lee, Kyu-Chung;Hur, Chang-Wu
    • Journal of information and communication convergence engineering
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    • 제7권1호
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    • pp.72-77
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    • 2009
  • Three different procedures for adding Pd compounds to $SnO_2$ particles have been investigated. These processes are: (1) coprecipitation; (2) dried powder impregnation; and (3) calcined powder impregnation. The microstructures of $SnO_2$ particles have been analyzed by X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), scanning electron microscope (SEM) and X-ray photoelectron spectroscopy (XPS). In the coprecipitaion method, the process does not restrain the growth of $SnO_2$ particles and it forms huge agglomerates. In the dried powder impregnation method, the process restrains the growth of $SnO_2$ particles and the surfaces of the agglomerates have many minute pores. In the calcined powder impregnation method, the process restrains the growth of $SnO_2$ particles further and the agglomerates have a lot more minute pores. The sensitivity ($S=R_{air}/R_{gas}$) of the $SnO_2$ gas sensor made by the calcined powder impregnation process shows the highest value (S = 21.5 at 5350 ppm of $C_3H_8$) and the sensor also indicates the lowest operating temperature of around $410^{\circ}C$. It is believed that the best result is caused by the plenty of minute pores at the surface of the microstructure and by the catalyst Pd that is dispersed at the surface rather than the inside of the agglomerate. Schematic models of Pd distribution in and on the three different $SnO_2$ particles are presented.

4HBA 변성 하이솔리드 아크릴 우레탄 도료의 반응성 및 물성 연구 (A Study on the Reactivity, Performance of 4HBA Modified High Solid Acrylic Polyurethane Paint)

  • 서석환;서차수;박진환
    • 공업화학
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    • 제20권1호
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    • pp.52-61
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    • 2009
  • 본 연구에서는 2액형 아크릴 우레탄 도료에 있어서 바인더로 사용되는 하이솔리드 아크릴 폴리올 수지를 개발함에 있어서 핵심요소인 반응 개시제로 TAPEH (t-amyl peroxy 2-ethyl hexanoate)를 선택하였다. 그리고 하이드록시 모노머는 Tone M100 (caprolactone acrylate), 4HBA (4-hydroxy butyl acrylate), 2HEMA (2-hydroxy ethyl methacrylate)를 사용하였다. 앞의 물질을 2액형 아크릴 우레탄 도료용으로 응용함에 있어서 적용성과 VOC 저감을 위하여, 알리파틱 폴리이소시아네이트 경화제 종류에 따른 반응성과 도막물성을 검토하였다. 또한 최근 주석계 촉매의 사용 억제에 따라 저독성 금속촉매와의 반응성 및 물성도 비교 시험하였다. 이상의 결과로부터 2액형 하이솔리드 폴리우레탄 수지 도료의 응용에 필요한 기초자료 확보로 도막물성과 작업성 개량 및 친환경 도료개발에 효과적으로 응용 할 수 있는 것을 검토하였다.