• Journal of the korean academy of Pediatric Dentistry
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• v.25 no.2
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• pp.259-267
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• 1998

For more than two decades, many investigators have tried a variety of methods for delivering antimicrobial agents to the oral cavity with the objective of eliminating mutans streptococci. In the belief that the effectiveness of chemotherapy might be improved by a more effective delivery system, the intention of the present study was to exploit a new drug delivery system delivering chlorhexidine to the oral cavity. The vehicle delivering chlorhexidine tested in this study was self-curing acrylic resin(polymethyl methacrylate). The powder of the acrylic resin was polymerized with the 5 different liquid preparations, in which $Chlorzoin^{(R)}$ was mixed with five different monomer/Chlorzoin ratios immediately prior to the polymerization, in a stainless steel mold ($40mm{\times}40mm{\times}2mm$). A total of 50 cured resin specimens were divided into 5 groups according to the different monomer preparations. Every specimen was soaked in an airtight container filled with distilled water (100 ml) and then kept in an incubator at $37^{\circ}C$. The solutions (0.8 ml) were collected from the container at every 24 hours, and the amount of released chlorhexidine in the solutions was measured in an ultraviolet spectrophotometer at 250nm. The container was refilled with distilled water every after measurement. This procedure was repeated for 14 days. It was found that chlorhexidine was continuously released from all of the 50 specimens during the experimental period. And it was noted that the pattern of chlorhexidine release was a type of sustained-release preparation, that is, the amount of the released chlorhexidine at the first day in all 5 groups was high (p<0.0001), and then the release was decreased during the rest of the experimental period (p<0.001).

• Clean Technology
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• v.13 no.3
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• pp.208-214
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• 2007

Environmentally-friendly acrylic resin particles having the diameter between $0.1\;and\;1\;{\mu}m$ were prepared using non-aqueous dispersion (NAD) polymerization technique. The first step is to prepare the stabilizer and the next step is the NAD polymerization by dropping an acrylic monomer to stabilizer dispersed in organic media. To obtain a NAD resin with proper level of viscosity, it fumed out that stabilizers having sufficient viscosity such as 1000 cP need to be used, for which the stepwise feeding of monomer and initiator was necessary. It was necessary to put proper amount of stabilizer, but no more increase in viscosity was observed when more than that amount of stabilizer was added. Choice of proper monomers considering solubility parameter was essential to avoid the bimodal particle size distribution in the NAD resin product.

• Journal of Adhesion and Interface
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• v.9 no.1
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• pp.16-21
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• 2008

Hybrid emulsions consisting of polyurethane and acrylic polymer were prepared by emulsion polymerization of acrylic monomers and polyurethane water dispersions (PUD) as an emulsifier. At first, cationic type of PUD was synthesized with IPDI, PTMG1000, MDEA, and acetic acid. Then, acrylic monomers, such as MMA and n-BA, were copolymerized with the PUD without adding further surfactant. The tensile properties and water resistance increased with increasing acrylic monomer ratio. The hybrid emulsions showed better properties than the emulsions simply blended with the PUD and the acrylic emulsions.

• Textile Coloration and Finishing
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• v.10 no.3
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• pp.43-49
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• 1998

Polyvinyl chloride (PVC) sheets were treated with corona discharge to produce peroxy radicals on the surfaces. The peroxy radicals formed on the PVC surfaces were subsequently used as initiators for the graft polymerization of acrylic acid or acrylamide in an aqueous solution. Introduction of acrylic acid and acrylamide on the PVC sheet could be confirmed by the observation of carbonyl and primary amine absorptions based on carboxylic acid and amide, respectively. The water contact angle$(90^\circ)$ of PVC sheet was constant, irrespective of time, while corona-treated and functional monomer-grafted PVCs were slowly increased with time, showing the rearrangement of surface polar groups in air condition. The water contact angle of PVC sheet$(90^\circ)$ was decreased by corona treatment$(78^\circ)$, and further decreased by the grafting of acrylic acid$(55^\circ)$ and acrylamide$(56^\circ)$ , indicating increased hydrophilicity of the modified surfaces. The half-life periods of surface voltage on acrylic acid- (62 sec) and acrylamide-grafted PVC (147sec) were significantly decreased when compared to those on PVC (3,115 sec) and corona-treated PVC (463sec). These results mean that acrylic acid- and acrylamide-grafted PVCs could be used as the antistatic sheets.

• Proceedings of the Korean Fiber Society Conference
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• 2003.10b
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• pp.177-178
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• 2003

Many researchers have made efforts to control the stereoregularity in radical polymerization of vinyl monomers because the physical and chemical properties of the polymer are significantly affected by the stereostructure.[1]-[4] In general, monomer design, reaction conditions(e.g. solvent, temperature, and monomer concentration), and additives can alter the stereochemistry of the radical polymerization of acrylic monomer. (omitted)

• Proceedings of the Optical Society of Korea Conference
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• 2006.07a
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• pp.411-412
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• 2006

Photopolymers have been of considerable due to their easy of processing and high sensitivity. Exposure of photopolymers to optical source produce recroding mark where the light initiates a photoreaction that occurs preferentially in regions of high illumination. The photoreaction typically involves polymerization of an acrylic or epoxy monomer dispersed together with a photoinitiators in a polymeric binder. A number of photopolymerizable materials have been developed to apply them in 3D optical recording such as holographic or 3-dimensional data storage. In this presentation, photopolymers derived from sol-gel matrix and transparent polymer binder are summarized. The effect of monomer composition and plasticizers on optical recording will be discussed based on the monomer transport during the photopolymerization.

• The International Journal of Costume Culture
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• v.6 no.2
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• pp.134-146
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• 2003

Polyester of linear homopolymer poly(ethylene terephthalate)(PET) was chemically modified through the formation of branched copolymer to improve the undesirable properties of fiber. Photo-induced graft copolymerization of the acrylic monomers acrylic acid (AA) and methyl acrylate (MA) in the liquid and vapor phase, respectively, onto N,N-dimetylformamide (DMF)-pretreated PET fibers was carried out. The effect of various synthesis conditions and DMF pretreatment of the PET on the graft yield was investigated. Grafting mechanism was analysed. The grafting was promoted by increasing DMF pretreatment temperature and amount of DMF retention in the fiber. The increasing biacetyl and monomer flow time, and irradiation time enhanced the grafting up to a certain amount and thereafter it decreased.

• Fibers and Polymers
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• v.7 no.3
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• pp.223-228
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• 2006

Hydrogels of semi-interpenetrating polymer networks (semi-IPNs) were prepared by two step reactions. Dimethylaminoethyl methacrylate (DMAM) and poly(ethylene glycol)-dimethacrylate (PEGDM) were copolymerized to yield hydrogels, and then acrylic acid (AA) monomer were adsorbed in the hydrogels followed by polymerization of AA to produce semi-IPNs. The swelling behavior of semi-IPNs depends largely on pH of medium, showing that the degree of swelling of the semi-IPNs exhibits a minimum at pH 6.0. It is observed that the elastic modulus of semi-IPNs is closely related to its swelling behavior.

• Journal of the Korean Applied Science and Technology
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• v.18 no.2
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• pp.142-152
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• 2001

Acrylic resin(ACR) was blended with a curing agent, hexamethoxymethylmela-mine(HMMM), in which blending ratio was 70:30. The curing behavior was examined using Rheovibron. Cross-linking reaction started at $170^{\circ}C$ in 2 min of reaction and curing was completed in 10 min. It was found that the extent of cross-linking increased with the content of acetoacetoxyethyl methacrylate monomer in the ACR.

• Journal of the Korean Chemical Society
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• v.26 no.4
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• pp.235-246
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• 1982

The free radical polymerization and copolymerization of N-acetyl ${\alpha}$-aminoacrylic acid were investigated. From the result of kinetic investigation of N-acetyl ${\alpha}$-aminoacrylic acid in DMF at $60^{\circ}C$, a rate equation of $R_p$ = $k_p[M]^{0.97}[I]^{0.59}$ was obtained. The overall activation energy for the polymerization was found to be 25.2 kcal/mole. Copolymerization of N-acetyl ${\alpha}$-aminoacrylic acid with acrylic acid and styrene was carried out for the determination of monomer reactivity ratios. The monomer reactivity ratios for the monomer pairs determined at 70.0{\pm}0.1^{\circ}C$ using benzoyl peroxide as an initiator are; $r_1$(N-acetyl ${\alpha}$-aminoacrylic acid) = 0.49, $r_2$(acrylic acid) = 1.41, $r_1$(N-acetyl ${\alpha}$-aminoacrylic acid) = 0.44, $r_2$(styrene) = 0.91. The values of Alfrey-Price's Q and e parameters for N-acetyl ${\alpha}$-aminoacrylic acid were calculated to be 0.51 and 0.16 for the both systems. Differential thermal analysis and thermogravimetry showed that acrylic acid copolymers have poorer thermal stability as compared with the homopolymer of N-acetyl ${\alpha}$-aminoacrylic acid.