• 제목/요약/키워드: single gradient buffer

검색결과 6건 처리시간 0.021초

Gradient YZO Buffer Deposition on RABiTS for Coated Conductor

  • Kim, T.H.;Kim, H.S.;Ko, R.K.;Song, K.J.;Lee, N.J.;Ha, D.W.;Ha, H.S.;Oh, S.S.;Pa, K.C.
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2007년도 하계학술대회 논문집 Vol.8
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    • pp.240-241
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    • 2007
  • In general, high temperature superconducting coated conductors have intermediary buffers layer consisting of seed, diffusion barrier and cap layers. Simplification of the oxide materials buffer architecture in the fabrication of high temperature superconducting coated conductors is required because the deposition of multi-layers buffer architecture leads to a longer manufacturing time and a higher cost process of coated conductors. Thus, single buffer layer deposition seems to be important for practical coated conductor manufacturing process. In this study, a single gradient layered buffer deposition process of YZO for low cost coated conductors has been tried using DC reactive sputtering technique. About several thick YZO gradient single buffer layers deposited by DC co-sputtering process were found to act as a diffusion layer.

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자원제약조건을 갖는 연속흐름라인에서 Buffer 의 할당에 관한 연구 (The Buffer Allocation with Linear Resource Constraints in a Continuous Flow Line)

  • 성덕현;장수영;홍유신
    • 대한산업공학회지
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    • 제21권4호
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    • pp.541-553
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    • 1995
  • An efficient algorithm is proposed for a buffer allocation in a continuous flow line. The problem is formulated as a non-linear programming with linear constraints. The concept of pseudo gradient and gradient projection is employed in developing the algorithm. Numerical experiments show that the algorithm gives the actual optimal solutions to the problems with single linear constraint limiting the total buffer capacity. Also, even in longer production lines, it gives quite good solutions to the problems with the general linear resource constraints within a few seconds.

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Chromatographic Separation of Maltopentaose from Maltooligosaccharides

  • Lee, Jae-Wook;Kwon, Tae-Ouk;Moon, Il-Shik
    • Biotechnology and Bioprocess Engineering:BBE
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    • 제8권1호
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    • pp.47-53
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    • 2003
  • An experimental study on the chromatographic separation of maltopentaose from a mixture, including glucose, maltose, maltotriose, and maltopentaose, was carried out in a nonionic polymeric sorbent column while varying the operating conditions, such as the solution pH, buffer contents, and isopropyl alcohol (1PA) concentration. Unlike the pH and buffer contents, the IPA concentration had a Significant impact on the single component chromatograms for maltopentaose. The retention times of the maltooligosaccharides with the nonionic polymeric sorbent Sp207 were in the following order: glucose < maltose < maltotriose < maltopentaose. From the experimental binary, ternary, and quaternary chromatograms, gradient chromatographic separation with a changing IPA concentration as a function of time was required to obtain high-purity maltopentaose and reduce the elution time.

FPLC에 의한 Staphylococcal Enterotoxin A와 C의 동시분리 (Simultaneous Purification of Enterotoxin A and C by Fast Protein Liquid Chromatography)

  • 이정희;김종배;신현길
    • 한국식품과학회지
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    • 제20권6호
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    • pp.856-861
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    • 1988
  • 본 실험은 Staphylococcus aureus의 한 균주로부터 A와 C, 두 종류의 toxin이 동시에 생성될 때 이들의 동시분리를 위하여 각종 분리방법을 연구하였다. 혼합된 toxin A와 C는 CM-column chromatography를 이용하여 pH-gradient법으로 용출했을 때 2개의 분획이 나타났으나 서로 완전히 분리되지 않아 다량의 서로 다른 toxin이 함유되어 있었고 Sephadex G-75, Sephacryl S-300, 그리고 ultro gel을 사용한 gel filtration에서는 하나의 분획을 나타내 상호분리가 불가능 하였으며 정제도와 분리도에서 가장 뛰어난 gel column을 이용한 FPLC도 toxin A와 C를 상호분리할 수 없었다. 그러나 CM-column을 이용한 FPLC에서는 enterotoxin A는 pH 6.8에서 그리고 enterotoxin C는 pH 8.6에서 각각 분리되었으며, immunodiffusion test 결과 enterotoxin A의 분획에서는 toxin C가 전혀 검출되지 않았고 enterotoxin C의 분획에서도 toxin A가 검출되지 않았다. 용출방법에 있어서는 CM-column을 이용한 FPLC에서 pH-stepwise법이나 pH-gradient법으로 enterotoxin A와 C type을 쉽게 동시에 분리할 수 있었다.

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$S^{35}$(1,2-dichloro vinyl) L-Cysteine의 소에 의(依)한 대사물(代謝物)의 분리(分離)

  • 김재욱
    • Applied Biological Chemistry
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    • 제2권
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    • pp.36-39
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    • 1961
  • It has been ascertained that S-(1, 2-dichlorovinyl) L-cysteine (DCVC) is probably the toxic component in the trichloro-ethylene extracted soybean oil meal on the bovine. For the study of the metabolites of DCVC, the components with radioactive $S^{35}$-in the urine of the calf, to which $S^{35}$-DCVC was administrated, were separated using of cellulose powder with propanol-water (70:30 V/V) which is easily removable by evaporation. As the results followings were obtained: Peak 1, which shows fractions containing single $S^{35}$-radioactive components, whose Rf is 0.815 Peak 2, which shows fractions containing jingle $S^{35}$-radioactive component, whose Rf is 0.447 Peak 3, which shows fractions containing both $S^{35}$-radioactive components whose Rfs are 0.090 and 0.171 Peak 4, which shows fractions containing single $S^{35}$-radioactive component, whose Rf is 0.142. Peak 5, which shows fractions containing single $S^{35}$-radioactive component, whose Rf is 0.084. Besides these, two of small peak were obtained. Although, the resolving power of the cellulose powder column is not sufficient, it is applicable for the study of the components of metabolytes of DCVC conveniently with the rest of removable solvent easily. Also the components with radioactive $S^{35}$ in the feces of the calf were separated using citrate buffer gradient system of Moore and stein. As the results; three $S^{35}$-radioactive components were separated.

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A 54 kDa cysteine protease purified from the crude extract of Neodiplostomum seoulense adult worms

  • Choi, Min-Ho;Choe, Seong-Choon;Lee, Soon-Hyung
    • Parasites, Hosts and Diseases
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    • 제37권1호
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    • pp.39-46
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    • 1999
  • As a preliminary study for the explanation of pathobiology of Neodiplostomum seoulense infection. a 54 kDa protease was purified from the crude extract of adult worms by sequential chromatographic methods. The crude extract was subjected to DEAE-Sepharose Fast Flow column, and protein was eluted using 25 mM Tris-HC1 (pH 7.4) containing 0.05. 0.1, 0.2 and 0.4 M NaC1 in stepwise elution. The 0.2 M NaCl fraction was further purified by Q-Sepharose chromatography and protein was eluted using 20 mM sodium acetate (pH 6.4) containing 0.05, 0.1. 0.2 and 0.3 M NaCl, respectively. The 0.1M NaCl fraction showed a single protein band on SDS-PAGE carried out on a 7.5-15% gradient gel. The proteolytic activities of the purified enzyme were specifically inhibited by L-trans-epoxy-succinylleucylamide (4-guanidino) butane (E-64) and iodoacetic acid. The enzyme, cysteine protease. showed the maximum proteolytic activity at pH 6.0 in 0.1 M buffer, and degraded extracellular matrix proteins such as collagen and fibronectin with different activities. It is suggested that the cysteine protease may playa role in the nutrient uptake of N. seoulense from the host intestine.

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