• Proceedings of the Korean Vacuum Society Conference
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• 2011.02a
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• pp.366-366
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• 2011

냉중성자원은 하나로 반사체탱크에 위치한 수직공에 설치되어 노심에서 발생하는 열중성자를 감속재인 액체수소층을 통과시켜 냉중성자를 생산하는 설비로 수소가를 충전하고 있는 수소계통이 있으며, 21K의 극저온 액체수소/기체수소 2상(ttwo-phase)을 유지하기 위해 외부에서 유입되는 열침입을 최소화하기 위해 진공계통이 설치되어 있다. 진공계통은 수조내기기 집합체(In-Pool Assembly : IPA)의 액체수소 열사이펀, 감속재 용기 등의 냉중성자원 극저온 부풀들의 단열을 위하여 진공용기 내부진공도를 공정진공도 이하로 유지하기 위한 계통으로 고진공펌프, 진공배기탱크 및 저진공펌프의 조합으로 두 개의 진공펌프시스템과 진공박스, 배기수집탱크 및 밸브박스를 포함한 연결배관으로 설계되었다. 저진공펌프를 이용하여 대기압에서 고진공펌프 작동압력까지 도달한 후 고진공펌프를 가동하여 공정진공도 이하의 진공도를 확보하고, 고진공펌프로부터 배기되는 배출가스는 고진공펌프 후단에 설치된 진공배기탱크에 포집되며, 필요 시 저진공펌프레 의하여 배기수집탱크로 배출된다. 진공펌프시스템은 진공용기 내부의 압력이 공정진동고 이하로 유지되도록 연속적으로 가동되어 진공단열이 가능하다. 본 논문은 감속재인 수소를 액화상태로 유지하며, 공정진공도 이하로 충분히 유지되어 운전되는 진공계통의 특성을 원자로 운전 주기별로 소개하고자 한다.

• Proceedings of the Korean Vacuum Society Conference
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• 2011.02a
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• pp.361-361
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• 2011

하나로 냉중성자원(CNS: Cold Neutron Source)은 원자로 수조내 반사체 탱크에 위치한 수직 조사공에 설치되어 하나로 노심에서 발생하는 열중성자를 감속재인 액체 수소층을 통과시켜 냉중성자를 생산한다. 생성된 냉중성자는 유도관을 통하여 냉중성자 산란장치에 공급되어 이용 연구에 활용된다. 감속재로 사용되는 수소는 헬륨냉동계통의 운전에 따라 수소가 수조내기기 집합체(IPA: In Pool Assembly) 내로 이동되어 액화되어지므로, 극저온의 헬륨가스의 흐름이 중요하다. 헬륨냉동기에 의해 만들어진 극저온인 헬륨은 IPA 내의 수소와 열교환을 하기 위해서 배관을 통해 이동되며, 열손실없이 전달하기 위하여 헬륨 배관은 진공층이 형성된 이중배관으로 설계되어 있다. 헬륨 이중배관은 공급 및 회수 배관으로 구성되어 있으며, 헬륨 배관의 외관에 진공층을 20개의 구간으로 나누어 제작 및 설치되었으며, 각각의 진공도를 유지하고 있다. 이 논문에서는 하나로 냉중성자원 헬륨 이중배관의 특성과 헬륨냉동계통의 운전 및 정지시 온도 변화에 따른 이중배관 진공도의 변화를 분석하였다.

• Proceedings of the Membrane Society of Korea Conference
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• 2008.05a
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• pp.271-272
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• 2008

• Korean Journal of Microbiology
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• v.22 no.3
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• pp.175-181
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• 1984

In order to develope a protoplast fusion system for industrial coryneform bacteria, the optimum conditions for the formation and regeneration of progoplast were examined for Brevibacterium flavum and Corynebacterium glutamicum and the protoplast fusion was performed. For the formation of the protoplast of B. flavum and C. glutamicum, the optimum time for penicillin G. treatment to obtain protoplast was mid-exponential growth phase ($O.D_{580}=0.6-0.8,\;8.0{\times}10^7-1.0{\times}10^8cell/ml$). At the optimum conditions (0.3units/ml penicillin G and $400{\mu}g/ml$ lysoyme for treatement), frequencies of protoplast formation and protoplast regeneration were 99% and 25%, respectively. Protoplast regeneration frequency was highest under the optimum conditions for the protoplast formation. Addition of 25mM $Mg^{2+}\;and\;50mM\;Ca^{2+}$ to the regeneration medium further increased the regeneration frequencies. The protoplast fusion frequencies of B. flavum and C. glutamicum in intraspecies fusion were $1.0{\times}10^{-8}\;and\;7.8{\times}10^{-4}$, of the regenerated protoplast respectively, when 33% of PEG (polythylene glycol) 6,000 was used as the fusing agent.

• Transactions of the Korean Society of Automotive Engineers
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• v.13 no.5
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• pp.171-180
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• 2005

Bending performances of aluminum square tube beams reinforced by aluminum plates under three point bending loads have been evaluated using experimental tests combined with theoretical and finite element analyses. A finite element simulation for the three-point bending test was performed. Basic properties of aluminum materials used for initial input data of the finite element simulation were obtained from the true stress-true strain curves of specimens which had been extracted from the Al tube beams. True stresses were determined from applied loads and cross-sectional area records of a tensile specimen with a rectangular cross-section by real-time photographing, and true strains were obtained from in-situ local elongation measurements of the specimen gage portion by the multi-point scanning laser extensometer. Six kinds of aluminum tube beam specimens adhered by aluminum plates were employed fur the bending test. The bending deformation behaviors up to the maximum load described by the numerical simulation were in good agreement with experimental ones. After passing the maximum load, reinforcing plate was debonded from the aluminum tube beam. An aluminum tube beam strengthened by aluminum plate on the upper web showed an excellent bending capability.

• Analytical Science and Technology
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• v.12 no.4
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• pp.346-353
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• 1999

For the non-destructive multi-elemental analysis of environmental and biological materials, instrumental neutron activation analysis (INAA) was applied for the determination of toxic and trace elements in a set of three Algae samples provided by the International Atomic Energy Agency (IAEA). The analytical quality control was evaluated by comparing the analytical results of two standard reference materials of the National Institute of Standards and Technology (NIST); Oyster Tissue (SRM 1566a) and Citrus Leaves (SRM 1572). According to given analytical procedure, the concentration of 15-25 elements including spiked elements such as As, Cd, Cr and Hg in Algae samples were determined. To identify and validate these results, a data intercomparison program using more than 35 analytical methods in 150 laboratories was carried out and the estimated statistical data are summarized. Result of INAA is favorable, therefore, it is illustrated that can be applied for routine analysis of essential and toxic elements in algae samples as well as analytical quality assurance.

• Analytical Science and Technology
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• v.12 no.3
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• pp.184-189
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• 1999

$^{51}V$ NMR and cyclic voltammetry studies on the interaction of vanadate and N-benzyliminodiacetate (Bz-IDA) in aqueous solution have been studied. From the NMR spectra two $^{51}V$ NMR peaks resulting at -515.5 and -500.1 ppm, due to the complexations between vanadate(V) and Bz-IDA at pH 5. has been observed. From the cyclic voltammograms the reduction-oxidation of the vanadate(V) complex has been found to be one-electron reaction.

• Journal of Pharmaceutical Investigation
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• v.28 no.2
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• pp.109-113
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• 1998

This study is purposed to develop the sustained release and bioavailability of piracetam (PA). The use of alginate beads as a means to achieve sustained release of piracetam was evaluated in comparison with that of piracetam alone. In the PA-sodium alginate(SA) beads was confirmed by differential scanning calorimetry thermogram(DSC), indicating a relative shift of an endometric peak of PA to higher temperature. The changes in dissolution rates from PA-SA beads and PASA beads coated by chitosan(CHO) were significantly slower than that of intact PA. The release rate of PA-SA in the gastric fluid was markedly decreased compared with that in the intestinal fluid, suggesting that PA is mostly released in the intestinal fluid. However, the PA/SA ratio scarcely affected the release profile. The blood concentration- time curves of PA, PA-SA and PA-SA-CHO were obtained by oral administration to rats. $T_{max}$ of PA, PA-SA and PA-SA-CHO were 1, 10 and 6 hours, respectively. It was confirmed that the release of PA was prolonged by the formulation of PA-SA beads and PA-SA-CHO beads.

• Textile Coloration and Finishing
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• v.25 no.4
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• pp.292-302
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• 2013

Cotton fabrics treated with hybrid materials were developed and prepared. A halogen-free flame retardant and an aromatic amide were blended and applied to cotton fabrics. Thermal and physical properties of the treated cotton fabrics were investigated. The surface of the pure and coated cotton fabrics was characterized by Fourier transform infrared spectroscopy. The elemental composition of the coated surface of the cotton fabric was measured using X-ray photoelectron spectroscopy and compared with that of pure cotton fabric. After being solved in N,N-dimethylacetamide, m-aramid and triphenylphosphine oxide (TPP) were applied to cotton fabrics through a dip-pad-coagulation process. The treated cotton fabrics with recycled m-aramid/TPP resulted in increased limited oxygen index values and thermal resistance.

• The Journal of the Korean Society for Microbiology
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• v.35 no.4
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• pp.283-288
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• 2000

The PCR primer set JW21-JW22 of Weiss et al. (19), which was reported to amplify a 139-bp fragment of the l6S rRNA gene of Helicobacter pylori, has been recently used for the detection of H. pylori in clinical specimens. However, when we applied JW21-JW22 PCR to other members of the genus Helicobacter and unrelated microorganisms, all of these bacteria produced a 139-bp PCR product. Therefore, we designed a novel primer set, HPU185-HPL826, which produced a 642-bp amplicon of the l6S rRNA gene of H. pylori. Then we further examined the specificity of the novel PCR assay using Southern blot hybridization with an internal probe, HPP225. The PCR assay described in this study was shown to be highly sensitive and specific only to the H. pylori 16S rRNA gene sequences.