• 한국식품과학회지
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• 제27권3호
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• pp.370-374
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• 1995

Aspergillus niger CF-34가 생산하는 대두세포벽분해 효소 복합액을 알칼리로 처리하여 조효소액 중에 함유된 protease만을 선택적으로 제거할 수 있었다. 조효소액을 알칼리로 처리하였을 때 세포벽분해활성에는 영향을 적게 주고, 대두 단백질을 분해시켜 쓴 맛의 peptide를 생성하는 protease만을 선택적으로 불활성화시킬 수 있었다. 조효소액의 pH를 $9.0{\pm}0.1$로 조절하여 $20^{\circ}C$에서 약 30분 동안 서서히 교반한 후 다시 pH를 5.0로 조절하는 것이 최적 조건이었다. 이때 조효소액 중 protease 활성은 초기의 약 10% 미만으로 감소하였으며, 각 효소의 잔존 활성을 살펴보면 pectinase는 약 80%, polygalacturonase는 약 85%, xylanase는 약 95%, carboxymethyl cellulase는 약 100% 정도이었고, 대두세포벽분해활성은 초기의 약 90% 정도 유지할 수 있어 protease만이 선택적으로 제거되었다. 이렇게 처리된 효소액을 사용하여 비지 중의 대두 단백질을 추출할 경우 생산효율은 비록 감소하였지만, 대두단백질의 분해를 막고, 쓴맛 생성을 억제하여 품질 및 관능적으로 우수한 제품을 생산할 수 있었다.

• 한국분말재료학회지
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• 제20권3호
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• pp.180-185
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• 2013

The iron oxides nanoparticles and iron oxide with other compounds are of importance in fields including biomedicine, clinical and bio-sensing applications, corrosion resistance, and magnetic properties of materials, catalyst, and geochemical processes etc. In this work we describe the preparation and investigation of the properties of coated magnetic nanoparticles consisting of the iron oxide core and organic modification of the residue. These fine iron oxide nanoparticles were prepared in air environment by the co-precipitation method using of $Fe^{2+}$: $Fe^{3+}$ where chemical precipitation was achieved by adding ammonia aqueous solution with vigorous stirring. During the synthesis of nanoparticles with a narrow size distribution, the techniques of separation and powdering of nanoparticles into rather monodisperse fractions are observed. This is done using controlled precipitation of particles from surfactant stabilized solutions in the form organic components. It is desirable to maintain the particle size within pH range, temperature, solution ratio wherein the particle growth is held at a minimum. The iron oxide nanoparticles can be well dispersed in an aqueous solution were prepared by the mentioned co-precipitation method. Besides the iron oxide nanowires were prepared by using similar method. These iron oxide nanoparticles and nanowires have controlled average size and the obtained products were investigated by X-ray diffraction, FESEM and other methods.

• 한국식품영양과학회지
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• 제19권6호
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• pp.612-616
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• 1990

전상이 일어나기 직전의 W/O형 에멀젼에는 W/O형 에멀젼과 섞여 O/W/O 형 에멀젼이 생성한다는 것을 알았다. 그래서 W/O형 에멀젼 중에 분산된 O/W/O형 분산의 정도를 평가하기 위한 목적으로 시료 에멀젼(수상 :물, 유상 TGCR을 함유한 올리브유)을 원추 평판형 회전 점도계를 사용하여 전단속도 1.92-384sec$^{-1}$(온도 25$\pm$0.1$^{\circ}C$)에서 점도를 측정하고 이 값을 Mooney의 점도식에 대입하여 이론치와 실측치의 차로부터 O/W/O형 분산의 정도를 평가했다. O/W/O형 에멀젼의 생성은 전상 직전의 시료에서 높았고, 유화제인 TGCR의 농도가 낮을수록 O/W/O형 에멀젼의 생성이 증가되는 경향이 나타났다. 이러한 사실로부터 W/O형 에멀젼이 전상 직전 부근에서 이론적으로 설명할 수 없는 고점도 현상이 전상직전의 O/W/O형 에멀젼의 생성에 의해서도 일어날 가능성이 있다고 사료된다.

• 한국세라믹학회지
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• 제53권5호
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• pp.529-534
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• 2016

Nanocrystalline powder of zirconia stabilized with 8 mol% yttria (YSZ) has been synthesized through oxalate process using $ZrOCl_2{\cdot}8H_2O$ and $Y(NO_3)_3{\cdot}6H_2O$ as starting materials. Understanding of the characteristic changes of YSZ powder as a function of processing conditions is crucial in developing dense and porous microstructures required for fuel cell applications. In this research, microstructure change, surface area, particle shape and particle size were measured as a function of different processing conditions such as calcination temperature, stirring speed and concentration of starting materials. The resultant crystallite sizes were calculated by XRD-LB (X-Ray Diffraction Line-Broadening) method, BET method, and morphology of the crystal was observed in TEM and FE-SEM. The TEM examination showed that the powder synthesized with 0.7 M of YSZ concentration had a spherical morphology with sizes ranging from 20 to 40 nm. However, the powder was gradually aggregated above 1.0 M of YSZ concentration with the aggregation being intensified as the YSZ concentration was increased.

• 스마트미디어저널
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• 제8권3호
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• pp.95-103
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• 2019

세계 제조업은 장기적인 경기침체, 노동 원가 및 원자재 가격 상승으로 성장 한계에 봉착하게 되었으며, 이에 대한 해결방안으로 ICT와 센서 기술을 바탕으로 제조업의 4차 산업혁명을 진행하고 있다. 이러한 흐름에 따라 화학 산업에서의 스마트공장보급 확산과 스마트제조 기술 향상을 위해, 본 논문은 스마트 제조혁신을 위한 보호필름 공정 제조데이터 활용모델의 설계를 제안한다. 보호필름 공정 중에서 원료 배합 및 교반, 압출, 그리고 검수 공정에 대해서 온도, 압력, 습도, 그리고 동영상 및 열화상의 제조 데이터를 획득한다. 또한 획득된 제조 데이터는 대용량 스토리지에 저장되며, AI 서비스에 의한 시계열 및 이미지 분석과 시각화가 진행된다.

• 대한금속재료학회지
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• 제49권1호
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• pp.79-84
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• 2011

Double-walled carbon nanotubes (DWCNTs) with high purity were produced by the catalytic decomposition of tetrahydrofuran (THF) using a Fe-Mo/MgO catalyst at $800^{\circ}C$. The as-synthesized DWCNTs typically have catalytic impurities and amorphous carbon, which were removed by a two-step purification process consisting of acid treatment and oxidation. In the acid treatment, metallic catalysts were removed in HCl at room temperature for 5 hr with magnetic stirring. Subsequently, the oxidation, using air at $380^{\circ}C$ for 5 hr in the a vertical-type furnace, was used to remove the amorphous carbon particles. The DWCNT suspension was prepared by dispersing the purified DWCNTs in the aqueous sodium dodecyl sulfate solution with horn-type sonication. This was then air-sprayed on ITO glass to fabricate DWCNT field emitters. The field emission properties of DWCNT films related to transmittance were studied. This study provides the possibility of the application of large-area transparent CNT field emission cathodes.

• 대한금속재료학회지
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• 제48권4호
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• pp.335-341
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• 2010

High-quality single-walled carbon nanotubes (SWCNTs) were synthesized by catalytic decomposition of $C_2H_2$ using Fe-Mo/MgO catalyst at $800^{\circ}C$. The as-synthesized SWCNTs typically occurred in the form of a bundle with a diameter of 10~20 nm together with amorphous carbon and catalytic impurities, which were removed by a two-step purification process consisting of oxidation and an acid treatment. The oxidation step, using an $O_2$-Ar mixture at $380^{\circ}C$ for 5 hr in a vertical-type furnace and a $HNO_3$ treatment at $100^{\circ}C$ for one hour, was utilized to remove the amorphous carbon particles. Subsequently, metallic catalysts were removed in HCl at room temperature for 5 hr under magnetic stirring. The SWCNT suspension was prepared by dispersing the purified SWCNTs in an aqueous sodium dodecyl benzene sulfonate solution with horn-type sonication. This was then air-sprayed on glass to fabricate CNT field emitters. The samples had a turn-on field value of 4 V/${\mu}m$ and a current density of 0.67 mA/$cm^2$ at 9 V/${\mu}m$. Increasing the HCl treatment time improved the field emission properties.

• Fisheries and Aquatic Sciences
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• 제25권5호
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• pp.264-275
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• 2022

A non-destructive environmental DNA protocol for the genetic analysis of sea cucumber (Apostichopus japonicus) resources DNA was established. Among the several commercial DNA extraction kits, the DNeasy^® Plant Mini Kit was selected as the best choice to obtain the high-quality genomic DNAs from the mucous sea cucumber. As the temperature and incubation time increased, the amount of extracted environmental DNA was also large, but it was judged that the increased amount did not affect as much as 2-3 times. Therefore, these conditions were not considered to be the main factors to consider in actual environmental DNA extraction. However, the amount of seawater relative to the size of the sample was judged as a major consideration, and a sufficient amount of environmental DNA for analysis was secured when stored within 1 min while stirring the volume of seawater corresponding to the total sea cucumber weight (g). In securing the environmental DNA of sea cucumbers, the mortality rate of sea cucumbers in all experiments was 0, and it was judged that the effects of sea cucumbers were not significant through this treatment. Through the results of this study, sea cucumber DNA research, which has been conducted in a destructive method, can be conducted non-destructively through environmental DNA analysis. Through this study, we have secured a standard protocol that can successfully extract the sea cucumber DNA through environmental DNA. It is not only excellent in terms of time and cost of traditional DNA analysis method currently used, but it is completely non-destructive in the ecosystem of the survey area. It is believed that the system can be transformed in a way that does not affect it. However, it is thought that various standard protocols should be established considering the characteristics of each type.

• Corrosion Science and Technology
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• 제21권5호
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• pp.418-421
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• 2022

Stir-accelerated corrosion test of a high chromium cast iron was attempted in 0.1 mol dm^-3 H₂SO₄ + 0.05 mol dm^-3 HCl + 10 wt% SiC solution for 48 h at room temperature or at 45 ℃. The high chromium cast iron was composed of 2.8 wt% C and 27 wt% Cr and balanced with Fe. The high chromium cast iron was positioned into a 500 mL beaker with stirring of the solution at 1050 rpm using a magnetic hot plate. The corrosion rate was increased by agitating the solution. In addition, the corroded depth of the high chromium cast iron surface was increased by agitating the solution. The surface morphology of the high chromium cast iron after the stir-accelerated corrosion test revealed that a dendritic austenite phase partially remained in the corroded region after agitating the solution, indicating that solution movement during agitating could accelerate the corrosion rate of the high chromium cast iron.

• 공학기술논문지
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• 제6권2호
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• pp.125-129
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• 2013

In the pyrochemcial process of spent nuclear fuel, it is necessary to separate rare earth nuclides from LiCl-KCl eutectic waste salt for radioactive waste reduction. This paper presents the phosphorylation of neodymium chloride in LiCl-KCl-NdCl₃ system using Li₃PO₄-K₃PO₄ as a phosphorylation agent in a chemical reactor with pitched blade impellers. The phosphorylation test was performed changing operation temperature, stirring rate, and amount of phosphorylation agent. Neodymium chloride was effectively converted into neodymium phosphate (NdPO₄). It was confirmed that more than 99 wt% of neodymium can be separated from LiCl-KCl-NdCl₃ system using a phosphorylation method l