• 제목/요약/키워드: high-purity purification

검색결과 159건 처리시간 0.025초

고령토 침출용액으로부터 고순도 염화알루미늄 결정화 분리 (Crystallization and high purification of aluminium chloride hexahydrate from kaolin leaching solution)

  • 김우식;장희동
    • 한국결정성장학회지
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    • 제6권4호
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    • pp.584-594
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    • 1996
  • 본 연구에서는 고령토 침출용액으로부터 고순도의 염화알루미늄 결정을 분리하고자 침출용액의 용존 염화알루미늄의 농도, 결정화 온도 및 염소가스 주입속도 등의 결정화 조건이 염화알루미늄 결정의 순도에 미치는 영향에 대해 연구하였다. 결정의 순도는 침출용액의 염화 알루미늄의 과포화 농도 수준에 크게 영향을 받았다. 결정화의 조건에 따라 염화알루미늄의 과포화 농도가 낮게 형성되면 철이온의 함유가 낮은 고순도의 염화알루미늄 결정이 생성되었다. 침출용액 내의 과포화 농도 수준은 용액 내의 용존 염화알루미늄의 농도, 염산 농도, 결정화 온도 등에 의해 결정되었다. 그러나 이와 같은 결정화 조건의 변화에도 불구하고 염화알루미늄의 결정 모양은 침상형으로 일정하게 나타났다. 고령토 침출용액의 염산농도 측정을 위하여 Shank [9]가 제시한 Oxalate 적정법을 적용하였으며 고령토 침출용액과 같은 다성분 이온 용액에서도 정확한 염산 농도 측정이 이루어질 수 있음을 알 수 있었다.

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Isolation of Fucosterol from Pelvetia siliquosa by High-speed Countercurrent Chromatography

  • Hwang, Seung Hwan;Jang, Jai Man;Lim, Soon Sung
    • Fisheries and Aquatic Sciences
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    • 제15권3호
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    • pp.191-195
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    • 2012
  • We report here the use of high-speed countercurrent chromatography (HSCCC) in the preparative isolation and purification of the bioactive component, fucosterol, from Pelvetia siliquosa. A crude extract was obtained by ultrasonic extraction of powdered P. siliquosa using methylene chloride and was then subjected to separation and purification by HSCCC, coupled with evaporative light-scattering detection. Preparative HSCCC was performed successfully using a two-phase solvent system, n-heptane:methanol (3:2, v/v), to obtain 10.96 mg fucosterol with 96.8% purity from 50 mg of crude extract; the recovery rate was approximately 90.5%.

High-Level Production of High-Purity Human and Murine Recombinant Prion Proteins Functionally Compatible to In Vitro Seeding Assay

  • Hwang, Hae-Gwang;Kim, Dae-Hwan;Lee, Jeongmin;Mo, Youngwon;Lee, Se-Hoon;Lee, Yongjin;Hyeon, Jae Wook;Lee, Sol Moe;Cheon, Yong-Pil;Choi, Eun-Kyoung;Kim, Su Yeon;Lee, Yeong Seon;Son, Young-Jin;Ryou, Chongsuk
    • Journal of Microbiology and Biotechnology
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    • 제28권10호
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    • pp.1749-1759
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    • 2018
  • Recombinant (rec) prion protein (PrP) is an extremely useful resource for studying protein misfolding and subsequent protein aggregation events. Here, we report mass production of high-purity rec-polypeptide encoding the C-terminal globular domain of PrP; (90-230) for human and (89-231) for murine PrP. These proteins were expressed as His-tagged fusion proteins in E. coli cultured by a high cell-density aerobic fermentation method. RecPrPs recovered from inclusion bodies were slowly refolded under reducing conditions. Purification was performed by a sequence of metal-affinity, cation-exchange, and reverse-phase chromatography. The current procedure yielded several dozens of milligrams of recPrP per liter with >95% purity. The purified recPrPs predominantly adopted an ${\alpha}$-helix-rich conformation and were functionally sufficient as substrates to measure the seeding activity of human and animal prions. Establishment of a procedure for high-level production of high-purity recPrP supports the advancement of in vitro investigations of PrP including diagnosis for prion diseases.

메탄올 용매추출을 이용한 콜타르 흡수유 중의 인돌 결정화 (Indole Crystallization in Coal Tar Absorption Oil using Methanol Solvent Extraction)

  • 류희용;이상헌;신성순
    • 공업화학
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    • 제33권2호
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    • pp.166-172
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    • 2022
  • 콜타르 흡수유에 함유되어 있는 성분 중 고부가가치의 인돌을 효율적으로 분리, 회수 하기 위하여 추출-증류-결정화의 과정을 거치는 방법으로 천연 인돌 확보 기술을 연구하였다. 본 연구에 사용된 콜타르 흡수유의 주요 성분은 1.2% 나프탈렌, 0.1% 퀴놀린, 0.4% 이소퀴놀린, 6.4% 인돌, 21.0% 1-메틸나프탈렌, 48.8% 2-메틸나프탈렌 그리고 11.7% 비페닐을 포함하고 있다. 인돌의 분리, 정제를 위해 먼저 메탄올을 용매로 사용하여 콜타르 흡수유 중 인돌 성분을 추출상으로 분리한 후, 증류법으로 메탄올을 회수하였다. 계속해서 메탄올이 제거된 추출용액에 노말헥산을 혼합한 후 결정화하여 순도 99.3%의 인돌을 회수하였다. 또한 본 연구 결과를 바탕으로 개략적인 콜타르 흡수유 중 인돌 회수의 공정을 제안하였다.

Synthesis of High Purity Carbon Nano Fibers and Hydrogen from Propane Decomposition

  • Hussain, S.Tajammul;Gul, Sheraz;Mazhar, M.;Larachi, Faical
    • Bulletin of the Korean Chemical Society
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    • 제29권2호
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    • pp.389-392
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    • 2008
  • High purity carbon nano fibers/tubes (CNF/Ts) which contain 97% pure graphitic carbon are prepared by a new catalytic method. These carbon nano fibers/tubes are ready to use without any further purification. The striking feature of this method is the production of carbon nano fibers/tubes of narrow distribution range. The developed catalytic method also produces pure hydrogen. An additional advantage of this catalytic method is that catalyst can be reused without reactivation. Ni:Cu catalyst system is embodied into SCHOTT-DURAN filter disc of large pore size (40-100 mm). Due to the production of hydrogen in the reaction catalyst stability is enhanced and deactivation process is considerably slowed down.

강제대류시 고순도 Al괴의 응고조직에 미치는 유동의 영향 (A Study on the Effect of Fluid Flow on the Microstructure of High Purity Al Ingot under Forced Flow)

  • 김경민;김헌주;하기윤;윤의박
    • 한국주조공학회지
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    • 제13권6호
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    • pp.540-546
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    • 1993
  • The effects of fluid flow on the purification of aluminum were studied. As the revolution rate(N) increased, the size of columnar grain decreased gradually. The concentration of solidified crystal was decreased with increasing distance from chill and revolution rate(N). Distribution boundary layer thickness(${\delta}$) was calculated from the solute distribution obtained in solid experimentally and by use of BPS equation. The value of ${\delta}$ changed from about $60{\mu}m$ at N value of 27rpm to about $15{\mu}m$ at N value of 1000rpm. From this result, high purification was obtained by decreasing the diffusion boundary layer under forced convection.

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Use of Triton X-100 and Sephacryl S-500 HR for the Purification of Cymbidium Mosaic Virus from Orchid Plants

  • Han, Jung-Heon;La, Yong-Joon;Lee, Cheol-Ho
    • The Plant Pathology Journal
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    • 제15권1호
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    • pp.34-37
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    • 1999
  • Cymbidium mosaic virus (CyMV) was purified from CyMV infected orchid plant leaves by Sephacryl S-500 HR column chromatography. Partial purification was done by solubilization with Triton X-100 (alkylphenoxypolyethoxy ethanol) and precipitation with polyethylene glycol (PEG 6,000) followed by ultracentrifugation on 30% sucrose cushion. Based on the spectrophotometric analysis, 33 mg of CyMV could be obtained form 100 g of CyMV-infected orchid plant leaves. The purified CyMV represented one distinct homogeneous band by SDS-PAGE, and electron microscopy revealed that it was highly homogeneous and not fragmented. Bioassay demonstrated that the purified CyMV had a normal infectivity to Chenopodium amaranticolor and orchid plants. Based on these results, the purification method in this work could be served as an improved method for the purification of CyMV and similar viruses with good yield, high purity and native integrity.

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Recombinant Expression, Isotope Labeling, and Purification of Cold shock Protein from Colwellia psychrerythraea for NMR Study

  • Moon, Chang-Hun;Jeong, Ki-Woong;Kim, Hak-Jun;Heo, Yong-Seok;Kim, Yang-Mee
    • Bulletin of the Korean Chemical Society
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    • 제30권11호
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    • pp.2647-2650
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    • 2009
  • Cold shock proteins (Csps) are a subgroup of the cold-induced proteins on reduction of the growth temperature below the physiological temperature. They preferentially bind to single-stranded nucleic acids to translational regulation via RNA chaperoning. Csp plays important role in cold adaptations for the psychrophilic microorganism. Recently, Cold shock protein from psychrophilic bacteria, Colwellia psychrerythraea (CpCsp) has been identified. Three dimensional structures of a number of Csps from various microorganisms have been solved by NMR spectroscopy or X-ray crystallography, but structures of psychrophilic Csps were not studied yet. Therefore, cloning and purification protocols for further structural study of psychrophilic Csp have been optimized in this study. CpCsp was expressed in E. coli with pET-11a vector system and purified by ion exchange, size exclusion, and reverse phase chromatography. Expression and purification of CpCsp in M9 minimal media was carried out and $^{15}N$-labeled proteins with high purity over 90% was obtained. Further study will be carried out to investigate the tertiary structure and dynamics of CpCsp.

킬레이트제를 활용한 VRFB용 고순도 오산화바나듐 제조 연구 (Study on the Manufacture of High-purity Vanadium Pentoxide for VRFB Using Chelating Agents)

  • 김선경;권숙철;김희서;서용재;유정현;장한권;전호석;박인수
    • 자원리싸이클링
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    • 제31권2호
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    • pp.20-32
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    • 2022
  • 본 연구에서는 VRFB용 고순도 오산화바나듐을 제조하기 위한 불순물 분리 정제 공정에서 킬레이트제(EDTA)의 영향을 조사하였다. 저순도 바나듐 원료를 이용하여 제조된 바나듐 용액으로부터 NH4VO3 을 침전 회수하여 제조된 최종 V2O5 분말의 순도는 99.7%로 분석되었지만 NH4VO3 침전 회수 공정에서 킬레이트제를 첨가한 경우 최종 V2O5 분말 순도가 99.9% 이상으로 향상되었다. 이러한 결과는 첨가된 킬레이트제가 불순물 이온과 반응하여 complex를 형성하고 불순물 이온이 안정화되기 때문에 침전 회수 공정에서 바나듐에 대한 선택성이 향상된 것으로 판단된다. 하지만 제조된 V2O5 분말내에는 불순물 규격 대비 K, Mn, Fe, Na 및 Al 함유량이 높아 추가적인 불순물 정제 연구가 필요하였다. 고순도 V2O5 분말을 새롭게 개발된 직접 전해공정에 적용하여 바나듐 전해액을 제조하였고 이의 특성을 상용 전해액과 비교 분석하였다. 제조된 바나듐 전해액의 순도는 불순물 K, Ca, Na, Al, Mg 및 Si 성분의 높은 함량으로 인하여 상용 전해액의 순도 99.98%보다 낮은 99.97%로 분석되었다. 따라서 고순도 V2O5 분말 및 전해액 제조 공정의 불순물 분리 정제에 대한 추가적인 최적화 연구가 수행된다면 상용화가 가능한 공정이 개발될 것으로 기대된다.

Thioltransferase (Glutaredoxin) from Chinese Cabbage: Purification and Properties

  • Cho, Young-Wook;Park, Eun-Hee;Lim, Chang-Jin
    • BMB Reports
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    • 제31권4호
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    • pp.377-383
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    • 1998
  • Thioltransferase, also known as glutaredoxin, was purified from Chinese cabbage (Brassica campestris ssp. napus var. pekinensis) by a combination of ion-exchange chromatography and gel filtration. Its purity was confirmed by SDS-polyacrylamide gel electrophoresis and its molecular weight was estimated to be about 12,000 which is comparable with those of most known thioltransferases. The enzyme utilizes 2-hydroxyethyl disulfide, S-sulfocysteine, ${\alpha}-chymotrypsin$, insulin, and trypsin as substrates in the presence of reduced glutathione. The enzyme has Km values of 0.03-0.97 mM for these substrates. It appeared to contain dehydroascorbate reductase activity. The pH optimum of the enzyme was 8.5, when 2-hydroxyethyl disulfide was used as a substrate. It was greatly activated by reduced glutathione. Its activity was not significantly lost when stored at high temperature, indicating its thermostable character. It may play an important role in thiol-disulfide exchange in plant cells.

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