• The Korean Journal of Ceramics
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• 제6권3호
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• pp.229-235
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• 2000

The spherical silica powder was synthesized by varying the kinds of solvent and mixing energy in emulsion method. The stirring speed varied from 500 to 1000 r.p.m. at 5$0^{\circ}C$ for 2h. Toluene in benzyl groups and a series of alkanes were used as dispersant. The average size of spherical silica particles decreased with increasing the stirring speed and the chain length o solvents used in this work. The average size was controlled in the range of 134~28$\mu\textrm{m}$ by selecting a proper solvent and stirring speed. The optimum processing parameters were described in details.

• Elastomers and Composites
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• 제33권2호
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• pp.110-116
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• 1998

A new technology was introduced to the emulsion polymerization. It is the ultrasonic activation method which replaced a chemical initiator and the environmentally benign process. In this study, free radicals were produced by a pulse type ultrasound energy irradiation, then polystyrene latex was polymerized without chemical initiator. With ultrasonic energy density, the degree of polymerization, average molecular weight, and particle size were increased, but the polydispersity index for the molecular weight and the particle size were decreased. The optimum condition of emulsifier concentration and temperature was found to be 1.0 wt.% SDS and $40^{\circ}C$, respectively. As a result, the emulsion polymerization process without chemical initiator was proved to be comparable to common latex properties such as average molecular weight, molecular weight distribution, particle size, etc.

• Journal of Ceramic Processing Research
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• 제13권spc1호
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• pp.145-148
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• 2012

Spherical silica aerogel powders were fabricated via an emulsion polymerization method from a water glass. A water-in-oil emulsion, in which droplets of a silicic acid solution are emulsified with span 80 (surfactant) in n-hexane, was produced by a high power homogenizer. After gelation, the surface of the spherical silica hydrogels was modified using a TMCS (trimethylchlorosilane)/n-hexane solution followed by solvent exchange from water to n-hexane. Hydrophobic silica wet gel droplets were dried at 80 ℃ under ambient pressure. A perfect spherical silica aerogel powder between1 to 12 ㎛ in diameter was obtained and its size can be controlled by mixing speed. The tapping density, pore volume, and BET surface area of the silica aerogel powder were approximately 0.08 g·cm-3, 3.5 ㎤·g-1 and 742 ㎡·g-1, respectively.

• 공업화학
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• 제9권2호
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• pp.294-299
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• 1998

입자당 한 개 이상의 성장라디칼이 있는 일반계에서 근사적인 psedo-homopolymerization (PHP)방법의 신뢰성을 간접적으로 증명하기 위하여, 벌크중합의 Mayo-Lewis식이 Interval II 동안 유화중합의 순간공중합조성식으로부터 확률적으로 유도됨을 보였다. Ballard등에 의하여 제안된 유화공중합의 확장된 Smith-Ewart식으로부터 0-1계(입자당 1개 이하의 성장라디칼이 있는 계)에 대하여 완전해를 얻었다. 이 해를 사용하여 입자당 평균라디칼수와 순간공중합조성이 몇 분 이내에 정상상태에 도달함을 예측할 수 있었다. 따라서 0-1계에 국한하여 PHP근사방법의 신뢰성을 직접 증명할 수 있었다. 모델계산의 목적으로 Styrene-butadiene(St-Bu)과 Styrene-methyl methacrylate(St-MMA)계를 예로 들었다.

• 한국응용과학기술학회지
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• 제21권3호
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• pp.191-196
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• 2004

An emulsion of octadecamidoethylaminoethyl dodecate (which provides softness) and an emulsion silicone oil KF-96 (which provides lubricity) were separately synthesized. Then PP finishing softeners (SSA-7) was prepared by blending of the synthesized emulsions with beef tallow hardened oil (a softness improving agent). PP finishing treatment was carried out with the prepared SSA-7 and PP finishing resin by a one bath method, and several physical properties were tested. As a result, crease recovery, tear strength, softness, lubricity, and bending resistance were all good, indicating that the prepared SSA-7 is a good PP finishing softener.

• 한국세라믹학회지
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• 제27권4호
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• pp.487-494
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• 1990

$Al_2O_3$-20w/o $ZrO_2$ composite powders were prepared by the emulsion-coprecipitation method and the effects of preparative conditions on powder characteristics were investigated. In the preparation of $Al_2O_3$-$ZrO_2$ composite powders, toluene was used instead of kerosene as the oil phase in emulsions. After coprecipitation, the emulsion was easily broken into a single liquid phase by adding methanol, and then precipitates could be effectively collected by filteration. The fact that all $ZrO_2$ phases present at room temperature in composite powders calcined at $1100^{\circ}C$ after washed by methanol had a tetragonal structure confirmed that methanol-washing enhanced the dispersibility of fine $ZrO_2$ particles in $Al_2O_3$ matrix. $Al_2O_3$-$ZrO_2$ composite powders were spherical particles of 0.2${\mu}{\textrm}{m}$ diameter. Pellets sintered at $1650^{\circ}C$ for 2hrs showed the relative theoretical density of 97.3% and the fracture toughness of 5.01MN/$m^{3/2}$.

• Bulletin of the Korean Chemical Society
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• 제33권7호
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• pp.2320-2324
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• 2012

A novel approach for metabolite extraction and fingerprinting was introduced based upon the nano-baskets and emulsion liquid membrane-nuclear magnetic resonance (ELM-NMR) technique. The objective of this method is optimizing the fingerprints, minimizing the metabolic variation from analysis, increasing the likelihood differences, and obtaining the maximum extraction yield. Low molecular weight metabolites in rat serum were recovered by ELMs using 12 nano-baskets of calixarene, as both emulsifier and carrier. The yields of ELMs were optimized by the method of one-at-a-time. According to NMR data, the maximum metabolic variation was achieved using scaffold 4 (4 wt %), n-decane membrane, stirring rate of 300 rpm, treat and phase ratios of 0.3 and 0.8, respectively. The results revealed that some calixarenes tend to extract non-specific macromolecules; and repeatability of fingerprints for 7-mediated ELM was maximum and for 3-mediated ELM was minimum. The yield of extractions was obtained to be higher for n-decane and lower for carbon tetrachloride. Among different membranes, the fingerprints by chlorinated liquid membranes were more repeatable than using toluene or n-decane.

• 한국재료학회지
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• 제16권6호
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• pp.355-359
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• 2006

Fine silica powders were synthesized via w/o emulsion method using sodium silicate, ammonium sulfate, Triton N-57, and cyclohexane as silica source, precipitating agent, surfactant, and oil phase, respectively. The powders were prepared under a conventional process and an ultrasonic process using the same reactants at room temperature for 1 hr varying the concentration of $Na_2SiO_3$ solution and the mol ratio of $H_2O$/surfactant, respectively. The particle size of the silica powder was reduced with decreasing the concentration of sodium silicate solution and with increasing the mol ratio of $H_2O$/surfactant under with and without ultrasounds. The size of powder with ultrasounds was smaller than that without ultrasounds, which indicates that the application of ultrasound in the synthesis of silica powder is an efficient way to reduce particle size.

• 한국식품과학회지
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• 제31권4호
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• pp.1077-1083
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• 1999

다른 유지상(bulk, oil-in-water)에 친수성 항산화제로서 gallic acid를 소수성 항산화제로서 ${\delta}-tocopherol$을 처리하고, HLB(hydrophilic lipophilic balance)에 따른 유화제를 처리하여 기질의 차이에 따른 항산화제와 유화제가 유지의 산화안정성에 미치는 정도를 실험하였다. 유지는 정제하지 않은 콩기름을 사용하였고 bulk상에서 12일 경과시 gallic acid를 첨가한 처리구의 유도기간이 Rancimat method로 측정시 4.13인데 비해 ${\delta}-tocopherol$을 첨가한 처리구의 유도기간은 1.18로 친수성 항산화제를 처리한 것이 3배 정도의 유지산화지연효과를 보였다. 또한 유화제의 처리에 있어서는 lecithin을 처리한 것의 유도기간이 5.07로 tween 20 처리 2.23, span 60의 경우 2.9인것에 비해 산화안정성면에서 우수하였다. 이와 같은 결과는 과산화물가와 공액이중산함량에서도 같은 경향을 보였다. Emulsion상(oil-in-water)에서도 bulk상과 같은 경향을 보였으며 이것은 emulsion상에 소수성 항산화제를 처리한 것이 유지 산화안정성면에서 더 효과적이라는 결과와는 차이가 있는데 기질의 차이, 즉 정제하지 않은 시판 콩기름을 사용한 것에 의한 차이인 것 같다. Emulsion상에서 유지방구의 크기는 저장하면서 모든 처리구에서 작아지는 경향을 보였으며, 이것은 유지방구의 크기가 작아지면서 표면적이 증가하고 따라서 공기와 접하는 면이 커지게 되므로 유지상은 안정해지나 산화는 더 촉진되므로 상의 안정과 산화안정성의 적절한 설정기준이 필요할 것으로 보인다.

• Macromolecular Research
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• 제9권5호
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• pp.267-276
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• 2001

In order to endow with new bioactive functionality from demineralized bone particle (DBP) as natural source to poly(L-lactide) (PLA) synthetic biodegradable polymer, porous DBP/PLA as natural/synthetic composite scaffolds were prepared and compared by means of the emulsion freeze drying and solvent casting/salt leaching methods for the possibility of the application of tissue engineered bone and cartilage. For the emulsion freeze drying method, it was observed that the pore size decreased in the order of 79$\mu\textrm{m}$ (PLA control) > 47$\mu\textrm{m}$ (20% of DBP) > 23 $\mu\textrm{m}$ (40% of DBP) > 15$\mu\textrm{m}$ (80% of DBP). Porosities as well as specific pore areas decreased with increasing the amount of DBR. It can be explained that DBP acts like emulsifier resulting in stabilizing water droplet in emulsion. For the solvent casting/salt leaching method, a uniform distribution of well interconnected pores from the surface to core region were observed the pore size of 80 ∼70 $\mu\textrm{m}$ independent with DBP amount. Porosities as well as specific pore areas also were almost same. For pore size distribution by the mercury intrusion porosimeter analysis between the two methods, the pore size distribution of the emulsion freeze drying method was broader than that of the solvent casting/salt leaching method due to the mechanism of emulsion formation. Scaffolds of PLA alone, DBP/PLA of 40 and 80%, and DBP powder were implanted on the back of athymic nude mouse to observe the effect of DBP on the induction of cells proliferation by hematoxylin and eosin staining for 8 weeks. It was observed that the effect of DBP/PLA scaffolds on bone induction are stronger than PLA scaffolds, even though the bone induction effect of DBP/PLA scaffold might be lowered than only DBP powder, that is to say, in the order of DBP only > DBP/PLA scaffolds of 40 and 80% DBP > PLA scaffolds only for osteoinduction activity. In conclusion, it seems that DBP plays an important role for bone induction in DBP/PLA scaffolds for the application of tissue engineering area.