• 폴리머
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• 제36권2호
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• pp.216-222
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• 2012

콘크리트 제조 시 잉여수의 지연 흡수를 위하여 가교된 crosslinked poly(styrene-$alt$-maleic anhydride)(PSMA)가 core이고, PSMA가 shell인 마이크로캡슐 흡수제를 침전중합법으로 제조하였다. Shell의 두께를 조절하기 위하여 (core 단량체의 질량)/(shell 단량체의 질량) 비가 1/1, 1/2 및 1/3이 되도록 하여 cPSMA-PSMA를 중합하였다. FTIR spectrometer를 사용하여 시멘트 포화 수용액 내에서 PSMA가 가수 분해 반응이 일어남을 확인하였다. TEM 분석으로 core/shell 단량체 비가 1/2(cPSMA #3)일 때 마이크로캡슐 구조를 잘 형성하는 것을 관찰하였고, 1/1(cPSMA #2)과 1/3(cPSMA #4)은 불완전한 마이크로캡슐 구조임을 관찰하였다. 시멘트 포화 수용액에서 cPSMA #3의 팽윤비는 초기 20분까지 증가한 후 2시간까지는 감소하였으며, 그 후 24시간까지는 다시 증가하였다. 제조된 cPSMA #3을 시멘트 페이스트에 첨가한 후 시간에 따른 점도 측정 결과 1시간까지는 거의 변화가 없었지만, 그 후 급격한 점도 증가가 일어났다. Core로만 구성된 cPSMA #1을 0.5 wt% 첨가한 시멘트 모르타르의 압축강도는 무첨가 시멘트 모르타르에 비해 약 5% 높게 나타났으며, cPSMA #3을 첨가한 모르타르는 약 7% 증가로 가장 높게 나타났다.

• 폴리머
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• 제34권1호
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• pp.38-44
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• 2010

탄산칼슘/유기계 core-shell 입자를 제조하기 위해 core로는 침강성 탄산칼습을 사용하였고, shell로서는 여러 종류의 methyl methacrylate(MMA), ethyl acrylate(EA), n-butyl acrylate(BA), styrene(St), 2-ethylhexyl acylate(2-EHA)을 사용하여, 반응 온도 유화제, 개시제의 종류와 첨가량을 변화시킨 후에 유화중합을 시켜 최적의 유화중합 조건을 구하였다. 생성된 core-shell 입자의 구조는 FT-IR로, 입자크기와 형태는 입도 분석, SEM, TEM으로 각각 측정하였다. 그리고, 이 core-shell 입자에 부직포를 함침시켜 처리전후의 표면변화는 접촉각으로 확인하였다. 또한, 함침 처리 전후의 부직포/부직포 소재와 관능성 단량체 첨가한 부직포/부직포 소재의 박리 접착강도를 측정하여 상호 비교하였다. 탄산칼슘/유기 core-shell 입자 합성의 경우에는 유화제인 SDBS를 0.5 wt% 첨가한 탄산칼슘을 core로 하여 MMA와 0.1 wt% 농도의 APS를 단계적으로 주입하여 중합함으로써 탄산칼슘입자 표면에 단량체의 중합이 잘 유도될 수 있었으며 중합 도중에 새로운 중합체 입자의 생성이 적었다.

• 한국응용과학기술학회지
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• 제25권1호
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• pp.83-90
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• 2008

The core-shell latex particles were prepared by sequential emulsion polymerization using alkyl methacrylate as a shell monomer and potassium persulfate (KPS) as an initiator. We study the effects of core-shell structure of calcium carbonate/alkyl methacrlyate in the presence of an anionic surfactant sodium lauryl sulfate (SLS) and polyoxyethylene alkyl ether sulfate (EU-S133D)). The structure of core-shell polymer were investigated by measuring to the thermal decomposition of polymer composite using thermogravimetric analyzer and morphology of latex by transmission electron microscope (TEM).

• Bulletin of the Korean Chemical Society
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• 제30권7호
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• pp.1485-1488
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• 2009

A facile, seed-mediated preparation method of trimetallic Au@Pb@Pt core-shell nanoparticles is developed. Au nanoparticles are the template seeds onto which sequentially reduced Pb and Pt are deposited. The trimetallic core-shell structure is confirmed by UV-Vis spectroscopy, TEM and EDS analysis, and cyclic voltammetry. The trimetallic Au@Pb@Pt core-shell nanoparticles show high electrocatalytic activity for formic acid and methanol electrooxidation.

• 폴리머
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• 제34권2호
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• pp.89-96
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• 2010

Methyl methacrylate(MMA), ethyl acrylate(EA), n-butyl acrylate(BA), styrene(St) 단량체를 수용성 개시제인 ammonium persulfate(APS)와 음이온 유화제인 sodium dodecyl benzene sulfonate(SDBS)를 사용하여 organic/organic core-shell 구조의 접착바인더를 중합 후 부직포와 피혁에 함침시키고 플라즈마 표면 처리 후 속도론적인 해석과 기계적인 물성을 평가하였다. Core-shell 바인더 중합시 전환율은 단량체의 조성이 등몰에서 MMA/EA, MMA/BA core-shell 복합입자 모두 90% 이상이 되었다. 등몰에서 부직포/부직포에 core-shell 복합입자를 함침시키고 플라즈마 처리 후의 상태접착 박리강도는 MMA/St, EA/BA, BA/MMA, EA/St, EA/MMA의 순으로 되었고, 또한 부직포/피혁에 core-shell 복합입자를 함침시키고 플라즈마 처리 후의 상태접착 박리강도는 MMA/BA, BA/EA, MMA/EA, St/MMA, EA/St의 순으로 되었다.

• Bulletin of the Korean Chemical Society
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• 제28권12호
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• pp.2279-2282
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• 2007

Highly crystalline, uniform Fe nanoparticles were successfully synthesized and encapsulated in zirconia shell using sol-gel process. Two different approaches have been employed for the coating of Fe nanoparticle with zirconia. The thickness of zirconia shell can be readily controlled by altering molar ratio of Fe nanoparticle core to zirconia precursor in the first case where as reaction time was found to be most effective parameter to controlled the shell thickness in the second method. The structure and magnetic properties of the ZrO2-coated Fe nanoparticles were studied. TEM and HRTEM images show a typical core/shell structure in which spherical α-iron crystal sized of ~25 nm is surrounded by amorphous ZrO2 coating layer. TGA study showed an evidence of weight loss of less than 2% over the temperature range of 50-500 °C. The nanoparticles are basically in ferromagnetic state and their magnetic properties depend strongly on annealing temperature. The thermal treatment carried out in as-prepared sample resulted in reduction of coercivity and an increase in saturation magnetization. X-ray diffraction experiments on the samples after annealing at 400-600 °C indicate that the size of the Fe@ZrO2 particles is increased slightly with increasing annealing temperature, indicating the ZrO2 coating layer is effective to interrupt growing of iron particle according to heat treatment.

• 한국분말재료학회지
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• 제25권5호
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• pp.420-425
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• 2018

Core-shell structured nanoparticles are garnering attention because these nanoparticles are expected to have a wide range of applications. The objective of the present study is to improve the coating efficiency of gold shell formed on the surface of silica nanoparticles for $SiO_2@Au$ core-shell structure. For the efficient coating of gold shell, we attempt an in-situ synthesis method such that the nuclei of the gold nanoparticles are generated and grown on the surface of silica nanoparticles. This method can effectively form a gold shell as compared to the conventional method of attaching gold nanoparticles to silica particles. It is considered possible to form a dense gold shell because the problems caused by electrostatic repulsion between the gold nanoparticles in the conventional method are eliminated.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
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• pp.531-531
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• 2012

So many groups have been researching the green quantum dots such as InP, InP/ZnS for overcoming the semiconductor nanoparticles composed with heavy metals like as Cd and Pb so on. In spite of much effort to keep up CdSe quantum dots, it does not reach the good properties compared with CdSe/ZnS quantum dots. This quantum dot has improved its properties through the generation of core/shell CdSe/ZnS structure or core/multi-shell structures like as CdSe/CdS/ZnS and CdSe/CdS/ CdZnS/ZnS. In this research, we try to synthesize the InP multi-shell structure by the successiveion layer absorption reaction (SILAR) in the one pot. The synthesized multi-shell structure has improved quantum yield and photo-stability. To generate white light, highly luminescent InP multi-shell quantum dots were mixed with yellow phosphor and integrated on the blue LED chip. This InP multi-shell improved red region of the LEDs and generated high CRI.

• 한국분말재료학회지
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• 제17권4호
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• pp.295-301
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• 2010

Multi shell graphite coated Ag nano particles with core/shell structure were successfully synthesized by pulsed wire evaporation (PWE) method. Ar and $CH_4$ (10 vol.%) gases were mixed in chamber, which played a role of carrier gas and reaction gas, respectively. Graphite layers on the surface of silver nano particles were coated indiscretely. However, the graphite layers are detached, when the particles are heated up to $250^{\circ}C$ in the air atmosphere. In contrast, the graphite coated layer was stable under Ar and $N_2$ atmosphere, though the core/shell structured particles were heated up to $800^{\circ}C$. The presence of graphite coated layer prevent agglomeration of nanoparticles during heat treatment. The dispersion stability of the carbon coated Ag nanoparticles was higher than those of pure Ag nanoparticles.

• 한국염색가공학회지
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• 제17권3호
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• pp.26-33
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• 2005

EVA microsphere was prepared by a thermally induced phase separation. EVAL microsphere was made by a saponification on sheath of EVA microsphere. And microcapsule with EVA core-PU shell structure was synthesized by interfacial polymerization using diisocyanates with PEG in gelatin aqueous solution as the stabilizing agent. The effects of chemical structure of diisocyanate on the average particle size and distribution, morphology, color strength and friction fastness of core-shell particles were investigated to design microcapsule. The friction fastness of the fabrics printed with EVA core-PU shell microcapsules had the 4-5 grade.