• Polymer(Korea)
• /
• v.27 no.4
• /
• pp.358-363
• /
• 2003

Dispersion polymerization of acrylamide was carried out in the media of ethyl alcohol/water mixtures using hydroxypropyl cellulose and ammonium persulfate as steric stabilizer and initiator, respectively. The effects of concentrations of initiator and steric stabilizer, amount of monomer, polymerization temperature, ethyl alcohol/water ratio, and purification of monomer and nitrogen purge on the particle size of the latices and molecular weight of the polymers were investigated. The average particle diameter increased with increasing concentration of initiator, water content in ethyl alcohol/water media, and polymerization temperature, but decreased with monomer and stabilizer concentrations. The viscosity average molecular weight increased with increasing concentrations of monomer, steric stabilizer, and water content in dispersion media, but decreased with initiator concentration and polymerization temperature. The PAM polymers prepared with the purified monomer and the nitrogen purging before the reaction showed the highest molecular weight. In this study, PAM latices of 0.5∼2.4 $\mu\textrm{m}$ with 20000∼335000 in M$\_$v/ were prepared and the resulting PAM latices were all dissolved in water instantly.

• Polymer(Korea)
• /
• v.34 no.1
• /
• pp.38-44
• /
• 2010

Core-shell particles of inorganic/organic pair were synthesized from $CaCO_3$ absorbed sodium dodecyl benzene sulfonate(SDBS) surfactant. Shell components were synthesized by sequential emulsion polymerization. Various monomers were used as shell components such as methyl methacrylate(MMA), ethyl acrylate(EA), butyl acrylate(BA), and styrene(St). Ammonium persulfate(APS) was used as an initiator and 2-ethylhexyl acylate(2-EHA) was used as a functional monomer, In the $CaCO_3$/organic core-shell particle polymerization, $CaCO_3$ absorbed surfactant SDBS of 0.5 wt% was prepared first and then core $CaCO_3$ was encapsulated by emulsion polymerization. 0.1 wt% of APS was added sequentially to minimize the formation of new monomer particle during shell polymerization. The structure of inorganic/organic core-shell particles were characterized by measuring the decomposition degree of $CaCO_3$ using HCl solution, thermogravimetric analyzer, scanning electron microscope, and transmission electron microscope.

• Polymer(Korea)
• /
• v.24 no.5
• /
• pp.629-637
• /
• 2000

Dispersion polymerization of acrylamide in the media of t-butyl alcoho1/$H_2O$ mixtures at 30~5$0^{\circ}C$ in the presence of hydroxypropyl cellulose and ammonium persulfate as steric stabilizer and initiator, respectively, was carried out. It was studied the effects of concentrations of initiator and steric stabilizer, amount of monomer, polymerization temperature, t-butyl alcohol/$H_2O$ ratio, concentration of crosslinker, purification of monomer and nitrogen purge on the particle size of the resulting acrylamide latices and molecular weight of the latex-poly(acrylamide). In this study, poly(acrylamide) latices of 0.1~0.5 ${\mu}{\textrm}{m}$ with 470000~2080000 in (equation omitted) were prepared and the resulting PAM latices were all dissolved in water in stantly.

• Polymer(Korea)
• /
• v.34 no.4
• /
• pp.341-345
• /
• 2010

Effects of modification of silver nanoparticles on the polymerization rate and morphology of poly(methyl methacrylate)(PMMA)/silver microspheres prepared by suspension polymerization of MMA were investigated. The silver nanoparticles and their surface hydrophilicity played an important role in the polymerization rate and the morphology of poly(methyl methacrylate) (PMMA)/silver microspheres. The polymerization rate increased slightly with modified silver nanoparticles. PMMA/silver microspheres with conversion up to 85% were obtained in spite of the low polymerization temperature. Due to the change of hydrophilicity of silver nanoparticles, different appearances of the microspheres having golf ball-like convex surfaces or concave surfaces were observed. As the hydrophilicity of silver was decreased, stable nanocomposites were prepared.

• Restorative Dentistry and Endodontics
• /
• v.35 no.1
• /
• pp.51-58
• /
• 2010

Dental composites have improved significantly in physical properties over the past few decades. However, polymerization shrinkage and stress is still the major drawback of composites, limiting its use to selected cases. Much effort has been made to make low shrinking composites to overcome this issue and silorane-based composites have recently been introduced into the market. The aim of this study was to measure the volumetric polymerization shrinkage kinetics of a silorane-based composite and compare it with conventional methacrylate-based composites in order to evaluate its effectiveness in reducing polymerization shrinkage. Five commercial methacrylate-based (Beautifil, Z100, Z250, Z350 and Gradia X) and a silorane-based (P90) composites were investigated. The volumetric change of the composites during light polymerization was detected continuously as buoyancy change in distilled water by means of Archemedes' principle, using a newly made volume shrinkage measurement instrument. The null hypothesis was that there were no differences in polymerization shrinkage, peak polymerization shrinkage rate and peak shrinkage time between the silorane-based composite and methacrylate-based composites. The results were as follows: 1. The shrinkage of silorane-based (P90) composites was the lowest (1.48%), and that of Beautifil composite was the highest (2.80%). There were also significant differences between brands among the methacrylate-based composites. 2. Peak polymerization shrinkage rate was the lowest in P90 (0.13%/s) and the highest in Z100 (0.34%/s). 3. The time to reach peak shrinkage rate of the silorane-based composite (P90) was longer (6.7 s) than those of the methacrylate-based composites (2.4-3.1 s). 4. Peak shrinkage rate showed a strong positive correlation with the product of polymerization shrinkage and the inverse of peak shrinkage time (R = 0.95).

• Proceedings of the Korean Radioactive Waste Society Conference
• /
• 2015.10a
• /
• pp.287-288
• /
• 2015

• Journal of the Society of Disaster Information
• /
• v.19 no.2
• /
• pp.280-291
• /
• 2023

Purpose: As fire accidents happen at the production and storage sites of superabsorbent polymers for convenience of daily life, an experimental study was conducted to secure basic data to establish practical preventive measures against them. Method: The sample container (20cm width × 20cm length) was made into a rectangular cuboid with the heights of 3cm, 5cm, 7cm, and 14cm, respectively, to allow access to the infinite flat plane. The front and back of the container were covered with a 300-mesh stainless steel mesh for one-dimensional heat transfer. The sample container was placed in the center of the thermostatic bath, which was heated to a predetermined temperature by setting the thermostat program in advance, and it was determined to be 'ignited' when the central temperature of the sample rose by more than 20℃ above the set temperature, and "unignited" when it was maintained at an approximate value of the set temperature. Result: The critical autoignition temperature was calculated to be 217.5℃ when the height of the sample container was 3 cm, 212.5℃ when it was 5 cm, 202.5℃ when it was 7cm, and 187.5℃ when it was 14cm. The ignition induction time to reach the maximum temperature was 34hours for 3cm, 76hours for 5cm, 143hours for 7cm, and 318hours for 14cm. Conclusion: ① As the size of the container increased, the autoignition temperature decreased and the induction time to reach the maximum temperature increased. ② An apparent activation energy was calculated to be 44.92kcal/mol, with a correlation of 96.93%.

• Journal of the Korean Society of Food Science and Nutrition
• /
• v.33 no.7
• /
• pp.1186-1191
• /
• 2004

Bacillus sp. $\beta$-mannanase was purified by DEAE-sephadex ion exchange column chromatography. The partially purified P-mannanase exhibited maximum activity at pH 6.0 and 5$0^{\circ}C$, and was stable at a pH range of 5.5 to 7.0, and at temperature between 30 to 5$0^{\circ}C$. Konjac glucomannan was hydrolyzed by the purified $\beta$-mannanase, and then hydrolysates separated by 1st activated carbon column chromatography and 2nd sephadex G-25 gel filtration. The main hydrolysates were composed of D.P 5 and 7 glucomannooligosaccharides by TLC and FACE method. To investigate the effects of guar gum glucomannooligosaccharides on the in vitro growth of B. longum, B. bifidum, B. infantis, B. adolescentis, B. animalis, and B. breve, Bifidobacterium spp. were cultivated individually on the modified-MRS medium containing carbon SOUTce such as D.P 5, and D.P 7 glucomannooligosaccharides, respectively. B. longum grew up 4.6-fold and 5.3-fold more effectively by the replacement of D.P 5 and 7 glucomannooligosaccharides as the carbon source in a comparasion of standard MRS. Also, B. breve and B. animalis slightly grew up by the treatment of D.P 5 glucomannooligosaccharide.

• Proceedings of the Korean Fiber Society Conference
• /
• 2002.04a
• /
• pp.417-420
• /
• 2002

마이크로 캡슐에 관한 연구는 벽 혹은 내부 물질의 성질, 캡슐화의 방법, 내부 구성물질의 내구성과 안정성 그리고, 확산, 투과, 부식, 용해등에 의한 유출현상등을 중심으로 진행되어 왔으며$^{1.2}$ , 1980년대 후반부터 섬유의 열적 성능을 개선하고자 캡슐화된 상전이 물질을 이용한 연구들이 시작 되었다[3-4]. 본 연구에서는 온도 조절 기능을 가지고 온도 감응형 섬유로의 적용을 위하여 상전이 물질(phase change materials: PCMs)을 함유하는 마이크로 캡슐을 제조하여 그 특성을 분석하고자 하였다. (중략)

• Journal of the Korean Chemical Society
• /
• v.26 no.5
• /
• pp.282-290
• /
• 1982

Several cation exchanged-layer silicate catalysts were prepared from acid clay mainly consisted of montmorillonite, and their catalytic activities for the ethylene polymerization were studied at room temperature. It was found that over$Ni^{2+}$ -Mont, dimerization of ethylene to n-butene proceeded selectively.$Ni^{2+}$ -Mont was activated by evacuation at elevated temperature, giving a maximum temperature, 150$^{\circ}$C . The variations in catalytic activities were closely correlated to the acidity of the catalysts.$Cr^{3+}$ -Mont exhibited a high activity for the polymerization, showing, a maximum at the evacuation temperature of 450$^{\circ}C$. The active site in $Cr^{3+}$-Mont was considered to be $Cr^{3+}$ ion.