• 제목/요약/키워드: thermal gel

검색결과 600건 처리시간 0.028초

저온 경화형 에폭시 매트릭스 수지의 경화거동 및 화학유변학에 대한 연구 (Cure Behavior and Chemorheology of Low Temperature Cure Epoxy Matrix Resin)

  • 나효열;염효열;윤병철;이성재
    • 폴리머
    • /
    • 제38권2호
    • /
    • pp.171-179
    • /
    • 2014
  • 우수한 성능을 지닌 대형 구조의 섬유강화 고분자(FRP) 복합재료 제품을 제조하기 위해 저온 경화형 프리프레그 개발이 활발히 진행되고 있다. 본 연구에서는 저온 경화형 프리프레그 제조에 적합한 매트릭스 수지를 확보하기 위하여 에폭시 수지, 경화제, 경화 촉진제로 구성된 저온 경화형 에폭시 수지 조성물의 경화거동 및 화학유변학을 고찰하였다. 경화반응 특성은 시차주사열량분석법과 유변물성측정법을 활용하여 승온 및 등온 조건에서 분석하였다. 연구 결과 매트릭스 수지로 제안된 저온 경화형 에폭시 수지 조성물은 $80^{\circ}C$에서 3시간에 경화시킬 수 있었고, 80과 $90^{\circ}C$에서의 젤화 시간은 각각 120분과 20분인 것으로 나타났다. 저온 경화형 수지를 경화시킨 수지 경화물의 열적, 기계적 물성은 고온 경화형 수지 경화물의 물성과 거의 동등하였다.

Overexpression, Purification, and Characterization of $\beta$-Subunit of Group II Chaperonin from Hyperthermophilic Aeropyrum pernix K1

  • Shin, Eun-Jung;Lee, Jin-Woo;Kim, Jeong-Hwan;Jeon, Sung-Jong;Kim, Yeon-Hee;Nam, Soo-Wan
    • Journal of Microbiology and Biotechnology
    • /
    • 제20권3호
    • /
    • pp.542-549
    • /
    • 2010
  • In the present study, overexpression, purification, and characterization of Aeropyrum pernix K1 chaperonin B in E. coli were investigated. The chaperonin $\beta$-subunit gene (ApCpnB, 1,665 bp ORF) from the hyperthermophilic archaeon A. pernix K1 was amplified by PCR and subcloned into vector pET21a. The constructed pET21a-ApCpnB (6.9 kb) was transformed into E. coli BL21 Codonplus (DE3). The transformant cell successfully expressed ApCpnB, and the expression of ApCpnB (61.2 kDa) was identified through analysis of the fractions by SDS-PAGE (14% gel). The recombinant ApCpnB was purified to higher than 94% by using heat-shock treatment at $90^{\circ}C$ for 20 min and fast protein liquid chromatography on a HiTrap Q column step. The purified ApCpnB showed ATPase activity and its activity was dependent on temperature. In the presence of ATP, ApCpnB effectively protected citrate synthase (CS) and alcohol dehydrogenase (ADH) from thermal aggregation and inactivation at $43^{\circ}$ and $50^{\circ}$, respectively. Specifically, the activity of malate dehydrogenase (MDH) at $85^{\circ}$ was greatly stabilized by the addition of ApCpnB and ATP. Coexpression of pro-carboxypeptidase B (pro-CPB) and ApCpnB in E. coli BL21 Codonplus (DE3) had a marked effect on the yield of pro-CPB as a soluble and active form, speculating that ApCpnB facilitates the correct folding of pro-CPB. These results suggest that ApCpnB has both foldase and holdase activities and can be used as a powerful molecular machinery for the production of recombinant proteins as soluble and active forms in E. coli.

Invention of Ultralow - n SiO2 Thin Films

  • Dung, Mai Xuan;Lee, June-Key;Soun, Woo-Sik;Jeong, Hyun-Dam
    • 한국진공학회:학술대회논문집
    • /
    • 한국진공학회 2010년도 제39회 하계학술대회 초록집
    • /
    • pp.281-281
    • /
    • 2010
  • Very low refractive index (<1.4) materials have been proved to be the key factor improving the performance of various optical components, such as reflectors, filters, photonic crystals, LEDs, and solar cell. Highly porous SiO2 are logically designed for ultralow refractive index materials because of the direct relation between porosity and index of refraction. Among them, ordered macroporous SiO2 is of potential material since their theoretically low refractive index ~1.10. However, in the conventional synthesis of ordered macroporous SiO2, the time required for the crystallization of organic nanoparticles, such as polystyrene (PS), from colloidal solution into well ordered template is typical long (several days for 1 cm substrate) due to the low interaction between particles and particle - substrate. In this study, polystyrene - polyacrylic acid (PS-AA) nanoparticles synthesized by miniemulsion polymerization method have hydrophilic polyacrylic acid tails on the surface of particles which increase the interaction between particle and with substrate giving rise to the formation of PS-AA film by simply spin - coating method. Less ordered with controlled thickness films of PS-AA on silicon wafer were successfully fabricated by changing the spinning speed or concentration of colloidal solution, as confirmed by FE-SEM. Based on these template films, a series of macroporous SiO2 films whose thicknesses varied from 300nm to ~1000nm were fabricated either by conventional sol - gel infiltration or gas phase deposition followed by thermal removal of organic template. Formations of SiO2 films consist of interconnected air balls with size ~100 nm were confirmed by FE-SEM and TEM. These highly porous SiO2 show very low refractive indices (<1.18) over a wide range of wavelength (from 200 to 1000nm) as shown by SE measurement. Refraction indices of SiO2 films at 633nm reported here are of ~1.10 which, to our best knowledge, are among the lowest values having been announced.

  • PDF

Immobilization of Fungal Laccase on Keratin-Coated Soil and Glass Matrices

  • Ginalska, G.;Lobarzewski, J.;Cho, Nam-Seok;Choi, T.H.;Ohga, S.;Jaszek, M.;Leonowicz, A.
    • Journal of the Korean Wood Science and Technology
    • /
    • 제29권3호
    • /
    • pp.112-122
    • /
    • 2001
  • Laccase enzymes from Cerrena unicolor and Trametes versicolor were immobilized on the activated glass beads (CPG), silica gel (SG) and soil (SL). The heterogeneous matrices were activated by ${\gamma}$-aminopropyltriethoxysilane (APTES) and glutaraldehyde (GA), and their surfaces were coated by keratin (KER) on activated or non-activated CPG, SG and SL. The laccase activities were tested in the aqueous solution for the native and immobilized preparations using different pH and temperature conditions. By keratin coating on supports, in the cases of CPG-KER and SL-KER, the immobilization yield was increased from about 80% to 90%. Moreover, much less protein was immobilized in keratin coated matrices than in inorganic ones alone (e.g. on CPG-KER 57.6%, whereas on CPG alone 80.6%). Laccase immobilization on keratin coated inorganic matrices was generally more effective than that of non-coated matrices. Concerned to pH dependency, the optima pH for immobilized laccases generally shifted towards to higher values, 5.5-5.8 and even 5.9 in the case of keratin for C. unicolor and from 5.3 to 5.7 for T. versicolor, respectively, and decreased less gradually both in acidic and alkaline regions. The immobilized laccase was more stable against thermal denaturation. This seems particularly true at $75^{\circ}C$ in the case of C. unicolor, where the activity of immobilized enzyme is > 50% higher than that of the free enzyme. For T. versicolor the respective values were $65^{\circ}C$, and 50%.

  • PDF

반응형 히드록시프로필 메틸셀룰로오스 프탈레이트를 이용한 셀룰로오스 혼성 폴리스티렌 나노입자의 합성 및 특성 분석 (Synthesis and Characterization of Cellulose-Hybrid Polystyrene Nanoparticles by Using Reactive Hydroxypropyl Methylcellulose Phthalate)

  • 정인우
    • 폴리머
    • /
    • 제30권5호
    • /
    • pp.437-444
    • /
    • 2006
  • Hydroxypropyl methylcellulose phthalate (HPMCP)에 isophorone diisocyanate (IPDI)와 2-hydroxyethyl methacrylate (HEMA)를 순차적으로 반응하여 우레탄 그룹을 형성하고 HPMCP에 비닐 그룹을 도입하여 반응형(reactive) HPMCP를 합성하였다. 제조된 반응형의 HPMCP와 반응전의 순수한 HPMCP의 분자량, 산가, 임계 미셀 농도(CMC) 등을 측정하였으며, 스티렌의 유화 중합에 고분자 유화제로서 도입하였다. HPMCP의 함량을 단량체인 스티렌 대비로 6, 9, 12, 18, 24 wt%로 도입하여 HPMCP 혼성 폴리스티렌 나노입자를 제조하고, 최대 중합 속도($R_{p,max}$), 입자당 평균라디칼 개수(n), 입자 크기 분포 등을 분석하였다. 또한 제조된 HPMCP 혼성 폴리스티렌 나노입자의 모폴로지를 TEM으로 분석하여 core-shell 구조임을 확인하였으며, TGA를 이용하여 열적안정성의 변화를 분석하였다. 반응형 HPMCP는 순수 HPMCP와는 달리 HEMA의 비닐 그룹으로 인해 높은 중합속도와 작은 입자 크기, 높은 표 값을 나타내었으며, 높은 젤 함량을 나타내었다.

막 축전식 탈염용 비불소계 아민화 Poly(vinylbenzyl chloride-co-ethyl methacrylate-co-styrene) 음이온교환막의 합성 및 특성 (Synthesis and Properties of Nonfluoro Aminated Poly(vinylbenzyl chloride-co-ethyl methacrylate-co-styrene) Anion Exchange Membranes for MCDI Process)

  • 구진선;곽노석;황택성
    • 폴리머
    • /
    • 제36권5호
    • /
    • pp.564-572
    • /
    • 2012
  • 본 연구에서는 막축전식 탈염(membrane capacitive deionization, MCDI) 공정용 음이온교환막의 제조를 위하여 vinylbenzyl chloride-co-ethyl methacrylate-co-styrene(VBC-EMA-St) 공중합체를 합성하였으며, 아민화 반응과 열처리를 통하여 음이온교환막을 제조하였다. 구조확인을 위하여 FTIR 분석을 하였고, GPC와 TGA를 통하여 합성한 고분자의 분자량과 분자분포, 열안정성을 분석하였으며, 함수율 및 이온교환용량을 측정하였다. 또한 LCR meter로 전기저항을 측정하고, MCDI 공정에 적용하기 위하여 제조한 음이온교환막을 충방전 시험 측정하였다. 이온교환용량, 함수율, 전기저항, 분자량은 각각 1.69 meq/g, 23.7%, 1.61 ${\Omega}{\cdot}cm$, $3.4{\times}10^4$ g/mol이었으며, CDI 충방전 시험 결과 상용화막인 AMX보다 우수한 성능을 나타내었다.

Amplicilin biosynthesis by immobilized enzyme

  • Kim, Young-Sik;Ryu, Dewy-D.Y.
    • Archives of Pharmacal Research
    • /
    • 제3권1호
    • /
    • pp.7-12
    • /
    • 1980
  • Ampliciline was synthesized from 6-amino-pencillanic acid (6-APA) and D-.alpha. phenylglycine methyl ester by using amplicilin synthesizing enzyme from Peudomonas melanogenum (IAM 1655). The whole cell enzyme was immobilized by entrapping it in the polyacrylamide gel lattices. The polymer used in the enzyme entrapment was made from 150 mg per ml of acrylamide monomer and 8 mg per ml of N, N'-methylenebisacrylamide. About 200 mg/whole cell enzyme was mixed in the polymer for entrapment. The maximal activity retention after immobilization was 56%. The optimal pH values for the whole cell enzyme and the immobilized whole cell enzyme were 6.0 and 5.9, respectively. The optimal temperature for the enzyme activity were the same for both type of preparations. The enzyme stabilities against pH and heat increased for immobilized whole cell enzyme. Immobilized cell was more stable especially in the acidic condition while both type were found to be very suceptible to thermal inactivation at a temperature above 4.deg.C. The kinetic constants obtained from Lineweaver-Burk plot based on two substate reaction mechanism showed somewhat higher value for immobilized whole cell enzyme as compared to the whole cell enzyme : the Km value for 6-APA were 7.0 mM and 12.5 mM while Km values for phenylglycine methyl ester were 4.5 mM and 8.2 mM, respectively. Using the immobilized whole cell enzyme packed in a column reactor, the productivity of ampiciline was studied by varying the flow rate of substrate solution. At the space velocity, SV, 0.14 hr$^{-1}$ the conversion was 45%. Operational stability found in terms of half life was 30 hr at SV = 0.2 hr.

  • PDF

Synthesis and Characterization of CZTS film deposited by Chemical Bath Deposition method

  • Arepalli, Vinaya Kumar;Kumar, Challa Kiran;Park, Nam-Kyu;Nang, Lam Van;Kim, Eui-Tae
    • 한국재료학회:학술대회논문집
    • /
    • 한국재료학회 2012년도 춘계학술발표대회
    • /
    • pp.99.1-99.1
    • /
    • 2012
  • The thin-film photovoltaic absorbers (CdTe and $Cu(In,Ga)Se_2$) can achieve solar conversion efficiencies of up to 20% and are now commercially available, but the presence of toxic (Cd,Se) and expensive elemental components (In, Te) is a real issue as the demand for photovoltaics rapidly increases. To overcome these limitations, there has been substantial interest in developing viable alternative materials, such as $Cu_2ZnSnS_4$ (CZTS) is an emerging solar absorber that is structurally similar to CIGS, but contains only earth abundant, non-toxic elements and has a near optimal direct band gap energy of 1.4 - 1.6 eV and a large absorption coefficient of ~104 $cm^{-1}$. The CZTS absorber layers are grown and investigated by various fabrication methods, such as thermal evaporation, e-beam evaporation with a post sulfurization, sputtering, non-vacuum sol-gel, pulsed laser, spray-pyrolysis method and electrodeposition technique. In the present work, we report an alternative aqueous chemical approach based on chemical bath deposition (CBD) method for large area deposition of CZTS thin films. Samples produced by our method were analyzed by scanning electron microscopy, X-ray diffraction, transmission electron microscopy, absorbance and photoluminescence. The results show that this inexpensive and relatively benign process produces thin films of CZTS exhibiting uniform composition, kesterite crystal structure, and some factors like triethanolamine, ammonia, temperature which strongly affect on the morphology of CZTS film.

  • PDF

반응압출법에 의해 개질된 폴리카프로락톤의 물성에 관한 연구 (Properties of Polycaprolactone Modified by Reaction Extrusion)

  • 신부영;장상희
    • 청정기술
    • /
    • 제12권4호
    • /
    • pp.198-204
    • /
    • 2006
  • 생분해성 고분자인 폴리카프로락톤을 반응개시제를 첨가하여 반응압출법으로 개질시켰다. 개시제의 함량은 중량 백분율로 0.1, 0.3, 0.5 그리고 1.0% 이었고 이축압출기의 온도는 $130{\sim}180^{\circ}C$로 운전하였다. 개질된 폴리카프로락톤에 대한 열분석, 분자량 분석, 기계적 강도 측정, 유변학적 특성 및 생분해도 연구를 수행하였다. 개질된 폴리카프로락톤은 순수 폴리카프로락톤과 비교하여 여러 물성에서 차이를 보였다. 개시제 1% 개질 폴리카프로락톤은 약 20%의 결정화도 감소, 약 50%의 인장탄성률 상승을 보였고, 복합점도, 유변학적 특성인 저장탄성률 및 손실탄성률의 큰 증가를 보여주었다. 0.1%의 가장 적은 개시제로 개질된 폴리카프로락톤의 생분해도는 순수 폴리카프로락톤과 비슷한 생분해도를 보였으나, 나머지는 생분해도가 증가하였다.

  • PDF

Effects of Mechanically Activated Milling and Calcination Process on the Phase Stability and Particle Morphology of Monoclinic Zirconia Synthesized by Hydrolysis of ZrOCl2 Solution

  • Lee, Young-Geun;Ur, Soon-Chul;Mahmud, Iqbal;Yoon, Man-Soon
    • 한국재료학회지
    • /
    • 제23권10호
    • /
    • pp.543-549
    • /
    • 2013
  • The purpose of this paper was to investigate the effect of a high-energy milling (HEM) process on the particle morphology and the correlation between a thermal treatment and tetragonal/monoclinic nanostructured zirconia powders obtained by a precipitation process. To eliminate chloride residue ions from hydrous zirconia, a modified washing method was used. It was found that the used washing method was effective in removing the chloride from the precipitated gel. In order to investigate the effect of a pre-milling process on the particle morphology of the precipitate, dried $Zr(OH)_4$ was milled using a HEM machine with distilled water. The particle size of the $Zr(OH)_4$ powder exposed to HEM reduced to 100~150 nm, whereas that of fresh $Zr(OH)_4$ powder without a pre-milling process had a large and irregular size of 100 nm~1.5 ${\mu}m$. Additionally, modified heat treatment process was proposed to achieve nano-sized zirconia having a pure monoclinic phase. It was evident that two-step calcining process was effective in perfectly eliminating the tetragonal phase, having a small average particle of ~100 nm with good uniformity compared to the sample calcined by a single-step process, showing a large average particle size of ~300 nm with an irregular particle shape and a broad particle size distribution. The modified method is considered to be a promising process for nano-sized zirconia having a fully monoclinic phase.