• 한국결정성장학회지
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• 제12권4호
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• pp.210-214
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• 2002

$450^{\circ}C$ 이하에서 Cu를 이용한 전계 유도 방향성 결정화 공정을 통해 비정질 실리콘의 결정화 거동을 고찰하였다. 열처리와 동시에 전계를 인가하여 Cu가 증착된 패턴의 외부에서 Cu가 존재하지 않는 비정질 실리콘의 영역으로 측면 결정화를 유도하였다. 특히, Cu가 존재하지 않는 영역의 측면결정화는 (-) 전극 쪽에서 (+) 전극 쪽으로 방향성을 가지고 결정화가 진행되었다. 이러한 현상은 Cu와 Si가 반응 할 때, 주확산 종이 금속(Cu)이기 때문에 가능하다고 판단되었다. 또한, FALC 공정을 이용한 $350^{\circ}C$의 온도에서 결정화된 영역 내에 커다란 dendrites 형태의 가지가 형성되었고 전계 방향에 따른 측면 결정화가 진행되었음을 확인하였다. 결론적으로 $350^{\circ}C$의 매우 낮은 온도에서 30 V/cm의 전계 인가를 통해 12$\mu$m/h의 결정화 속도로 결정화가 가능함을 확인하였다.

• 한국물환경학회지
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• 제21권1호
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• pp.59-65
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• 2005

A phosphate recovery system from artificial wastewater was developed using a completely mixed phosphorus crystallization reactor, in which powdered converter slag was used as a seeding crystal. In preliminary test, the optimal pH range for meta-stable hydroxyapatite crystallization for high phosphorus concentration was observed to be 6.0 to 7.0, which was different from the conventionally known pH range (8.0~9.5) for effective crystallization in relatively low phosphorus concentration less than 5 mg/L. The average phosphorus removal efficiency in a lab-scaled completely mixed crystallization system for artificial wastewater with about 100 mg/L of average $PO_4-P$ concentration was shown to be 60.9% for 40 days of lapsed time. XRD analysis exhibited that crystalline of hydroxyapatite formed on the surface of seed crystal, which was also observed in SEM analysis. In EDS mapping analysis, composition mole ratio (=Ca/P) of the crystalline was found to be 1.78, indicating the crystalline on the surface of seed crystal is likely to be hydroxyapatite. Particle size distribution analysis showed that average size of seed crystal increased from $28{\mu}m$ up to $50{\mu}m$, suggesting that phosphorus recycling from wastewater with high phosphorus concentration can be successfully obtained by using the phosphorus crystallization recovery system.

• 공학논문집
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• 제1권1호
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• pp.15-22
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• 1997

코디어라이트(2MgO.$2Al_2 O_3$.$5SiO_2$)계 유리와 겔을 일반 용융법과 졸겔법으로 제조하여 그 결정화 거동을 비교하여 보았다. 졸겔법으로 제조되는 겔의 치밀화 온도는 $810^{\circ}C$이었으며, IR결과 용융유리와 같은 구조를 가짐을 알 수 있었다. 겔의 결정화 개시온도는 $965^{\circ}C$이었으며, 핵형성제로서 10wt%의 $TiO_2$를 첨가한 용융유리의 $978^{\circ}C$ 보다 낮았다. 겔로부터의 결정상의 변화는 스피넬, $\beta$-석영고용 결정에서 $\alpha$-코디어라이트결정으로, 핵형성제로서 $TiO_2$를 넣은 용융유리에서는 (Mg,Al)TiOn 고용결정상과 $\beta$-석영고용결정에서 $\alpha$-코디어라이트로 전이하여감을 알 수 있었다. 핵형성제를 첨가한 용융유리의 결정화는 핵형성제로부터의 체적결정화였으며, 첨가하지 않은 경우는 $\beta$-석영고용결정으로부터의 표면결정화에 의해 결정화가 일어났으며, 겔로부터의 결정화는 치밀화과정에서 미립자사이에 생겨난 계면으로부터의 표면핵형성에 의한 내부 결정화과정을 거쳐 일어남을 알 수 있었다.

• 공업화학
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• 제29권6호
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• pp.799-804
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• 2018

결정화조작에 의해 접촉분해경유(LCO) 유분 중에 함유된 2,6-디메틸나프탈렌(2,6-DMN)의 분리 정제를 검토했다. LCO 유분을 원료로, 이소프로필알코올을 결정화 용매로 각각 사용하여 solute crystallization (SC)을 수행했다. 결정화 조작온도의 상승과 용매/원료의 체적비(S/F)의 증가는 2,6-DMN의 순도를 향상시켰으나, 역으로 수율의 저하를 초래시켰다. LCO 유분(13.9% 2,6-DMN)과 이소프로필알코올을 사용한 SC, SC에 의해 회수한 결정과 메틸아세테이트를 사용한 re-crystallization 1 (RC 1), RC 1에 의해 회수한 결정과 메틸아세테이트를 사용한 RC 2의 3단계로 결정화조작을 행한 결과, 19.5%의 수율로 99.9% 2,6-DMN의 결정을 회수할 수 있었다. SC, RC 1, RC 2의 각 조작을 통해 얻어진 실험적 결과를 이용하여 LCO 유분 중에 함유된 2-6-DMN의 분리 정제공정을 검토했다.

• 한국응용과학기술학회지
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• 제14권2호
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• pp.41-48
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• 1997

Separation of EPA and DHA from fish oil fatty acid ethyl ester (FAFE) by urea adductive crystallization method was carried out in the supercritical carbon dioxide (SC $CO_2$) as a solvent. Our results showed that SC $CO_2$ is a good candidate as a solvent in the urea adductive crystallization to separate FAFE by the number of unsaturated bonds. Compared to the separation process using methanol. SC $CO_2$ yielded better performance in the overall selectivity of EPA and DHA. The effect of process variables on separation of EPA and DHA was discussed in detailed. A hybrid technology of SC $CO_2$ fractionation and urea adductive crystallization with SC $CO_2$ was conformed as a viable process to separate and concentrate EPA and DHA from fish oil.

• 한국분말재료학회지
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• 제30권1호
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• pp.41-46
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• 2023

In this study, an Al₈₂Ni₇Co₃Y₈ (at%) bulk metallic glass is fabricated using gas-atomized Al₈₂Ni₇Co₃Y₈ metallic glass powder and subsequent spark plasma sintering (SPS). The effect of powder size on the consolidation of bulk metallic glass is considered by dividing it into 5 ㎛ or less and 20-45 ㎛. The sintered Al₈₂Ni₇Co₃Y₈ bulk metallic glasses exhibit crystallization behavior and crystallization enthalpy similar to those of the Al₈₂Ni₇Co₃Y₈ powder with 5 ㎛ or less and it is confirmed that no crystallization occurred during the sintering process. From these results, we conclude that the Z-position-controlled spark plasma sintering process, using superplastic deformation by viscous flow in the supercooled liquid-phase region of amorphous powder, is an effective process for manufacturing bulk metallic glass.

• 한국세라믹학회지
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• 제53권1호
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• pp.24-33
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• 2016

The grafting reaction for maleic anhydride (MA) onto high density polyethylene (HDPE) was investigated from solution process with initiators. The chemical modification of neat HDPE was carried out with various contents of MA (3-21 wt.%) and initiator (0.2-1 wt.%) at different temperature ($80-130^{\circ}C$). The grafting degree was obtained from the titration and the highest grafting degree was 3.1%. The grafting degree increased as the content of MA and initiator increased, however, the highest grafting degree was demonstrated for a particular content of MA and initiator. In the non-isothermal crystallization kinetics, the Ozawa model was unsuitable method to investigate the crystallization behavior of MA onto HDPE, whereas the Avrami and Liu models found effective. The crystallization rate was accelerated as the cooling rate increased, but postponed by combination of MA onto neat HDPE backbone.

• Macromolecular Research
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• 제14권2호
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• pp.146-154
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• 2006

Organic and inorganic hybrid nanocomposites based on poly(ethylene 2,6-naphthalate) (PEN) and silica nanoparticles were prepared by a melt blending process. In particular, polymer nanocomposites consisting mostly of cheap conventional polyesters with very small quantities of inorganic nanoparticles are of great interest from an industrial perspective. The crystallization behavior of PEN/silica hybrid nanocomposites depended significantly on silica content and crystallization temperature. The activation energy of crystallization for PEN/silica hybrid nanocomposites was decreased by incorporating a small quantity of silica nanoparticles. Double melting behavior was observed in PEN/silica hybrid nanocomposites, and the equilibrium melting temperature decreased with increasing silica content. The fold surface free energy of PEN/silica hybrid nanocomposites decreased with increasing silica content. The work of chain folding (q) for PEN was estimated as $7.28{\times}10^{-20}J$ per molecular chain fold, while the q values for the PEN/silica 0.9 hybrid nanocomposite was $3.71{\times}10^{-20}J$, implying that the incorporation of silica nanoparticles lowers the work required to fold the polymer chains.

• Macromolecular Research
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• 제17권7호
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• pp.476-482
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• 2009

The crystallization behavior of poly(vinyl alcohol) (PVA) in the presence and absence of polypyrrole nanoparticles (PPy NPs) was investigated in terms of the heterogeneous nucleation effect of PPy NPs using FTIR, X-ray diffraction, differential scanning calorimeter and polarized optical microscope analysis. PPy NPs were prepared by dispersion polymerization method stabilized by PVA in aqueous solution. A polymer nanocomposite with uniform dispersity could be readily obtained due to the enhanced compatibility between the filler and matrix. Compared with the PPy NP-absent PVA, the PPy NP/PVA nanocomposite exhibited an enhanced degree of crystallinity. The degree of crystallinity increased up to 17% at the PPy NP concentration of 1 wt%, compared to the pristine PVA. The PPy NP acted as an effective nucleating agent during the crystallization process, thereby enhancing the degree and rate of crystallization. The kinetics study of the crystallization also revealed the decreased value of the Avrami coefficient in the case of the PPy NP/PVA nanocomposite.

• 한국미생물·생명공학회지
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• 제42권3호
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• pp.232-237
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• 2014

본 연구에서는 반응액 부피당 표면적(surface area per volume of reaction solution)이 증가된 반코마이신 결정화 공정에서 표면적 증가물질인 실리카겔의 영향을 조사하였다. 표면적 증가물질로 실리카겔을 사용한 경우, 반코마이신 결정화 시간 단축 측면에서 표면적 증가물질인 실리카겔의 기공지름은 $40-60{\AA}$, 입자크기 230-400 mesh 범위가 적절함을 알 수 있었다. 또한 실리카겔의 첨가량이 증가 할수록 반코마이신의 결정 크기가 감소함을 확인할 수 있었다. 실리카겔을 표면적 증가물질로 사용함으로써 표면적 증가물질이 없을 때 보다 결정화에 소요되는 시간을 4배 정도 단축시킬 수 있었다. 이러한 개선된 결정화 방법은 반코마이신 정제 효율 향상에 상당히 기여할 것으로 판단된다.