• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 1997.11a
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• pp.489-492
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• 1997

Partial discharge characteristics of normal butyl acrylate grafted low density polyethylenes were investigated by an ultrasonic sensor made of ceramic piezoelectric material. It was found that the partial discharging activities in normal butyl acrylate grafted low density polyethylenes were considerably suppressed compared to those in plain low density polyethylene. It was found that acrylic acid grafted polyethylene was more effective than normal butyl acrylate grafted low density polyethylene.

• Journal of Adhesion and Interface
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• v.17 no.2
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• pp.56-61
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• 2016

This study was to investigate the effect of main monomer, butyl acrylate instead of 2-ethylhexyl acrylate, of acrylic PSAs on adhesive properties. The copolymers of butyl acrylate, acrylic acid and 2-hydroxyethyl acrylate were synthesized and their adhesive properties were investigated after crosslinking with two different agents. Comparing to 2-hydroxyethyl acrylate-based one which has branch-like side groups, butyl acrylate-based PSA with linear side groups show poor adhesive properties. In case of crosslinking agent, epoxy-typed agent than isocyanate-typed one showed better properties than isocyanate-typed one because epoxy-typed agent has more crosslinking sites and produces more flexible bonds, ester and ether, than isocynate-typed one. Most adhesive properties of PSAs were increased with acid content.

• Macromolecular Research
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• v.11 no.6
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• pp.425-430
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• 2003

Two types of poly(n-butyl acrylate) copolymer/silicate nanocomposites have been produced: poly(n-butyl acrylate-co-methyl methacrylate) [P(BA-co-MMA)]/silicate nanocomposites and poly(n-butyl acrylate-co-styrene) [P(BA-co-ST)]/silicate nanocomposites. The P(BA-co-MMA)/silicate nanocomposites shows the exfoliated structures but a P(BA-co-ST)/silicate nanocomposites have intercalated structures, because the BA/MMA comonomer has a higher polarity (e-value in Q-e scheme) than the BA/ST comonomer. The BA/MMA comonomer expanded the interlayer space of the silicate wider than did the BA/ST comonomer. The thermal degradation onset point of the P(BA-co-MMA)/silicate nanocomposites was 43$^{\circ}C$ higher than that of pure P(BA-co-MMA). P(BA-co-MMA)T5%, P(BA-co-MMA)T10%, and P(BA-co-MMA)T20% exhibit 134,302, and 195% increases, respectively, in their storage moduli at -20$^{\circ}C$ relative to the pure copolymer.

• Polymer(Korea)
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• v.35 no.4
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• pp.320-324
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• 2011

Two functional urethane acrylates were synthesized by using polycarprolactonediol (PCLD) and diisocyanate. The synthesized fuctional urethane acrylate was mixed with butyl acrylate(BA) or adhesion promoters, and their properties were investigated. To synthesize an excellent transparent urethane acrylate, isophorone diisocyanate(IPDI) was used. In addition, the effect of adding butyl acrylate for the improvement of shrinkage of urethane acrylate was studied. The results showed that the addition of butyl acrylate improved the shrinkage, and the optimum butyl acrylate content was 15 wt%. Both 2-ethyl hexyl acrylate (2-EHA) and ethyl acrylate(EA) were polymerized at $85^{\circ}C$ for 4 hrs to use as adhesion promoters, and the polymerized adhesion promoters were mixed to the UV-curing resin. The results showed that the adhesion properties increased with the increase of adhesion promoters content up to 15 wt%.

• Applied Chemistry for Engineering
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• v.10 no.6
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• pp.889-894
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• 1999

Preparation of micron size polymer particles which have desired morphology, size, and structure by emulsion polymerization is very difficult due to coagulation of latex particles and formation of second generation particles. But there are attractive merits such as preparation of structural and functional polymer particles in seeded emulsion polymerization. Seeded emulsion polymerization of n-butyl acrylate(BA) was carried out to investigate the effects of stirring rate, reaction temperature, concentration of initiator, emulsifier, and cross-linking agent on the particle size and size distribution. By the combination of suitable reaction conditions, we succeeded in preparing $0.14{\sim}3.67{\mu}m$ diameter of poly(n-butyl acrylate)(PBA) particles using sequential seeded emulsion polymerization.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 1996.11a
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• pp.278-282
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• 1996

Electrical properties of acrylic acid and n-butyl acrylate grafted polyethylene were investicated. Charge accumulation characterist-ics of acrylic acid grafted PE are changed by graft ratio, but it remains not changed in n-butyl acrylate grafted PE. It was also observed that anti-treeing and AC breakdown strength of grafted PE were increased due to the graft ratio. The change of electrical properties of grafted PE were attributed to the polar group introduced by the graft reaction.

• Journal of the Korea Concrete Institute
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• v.18 no.6 s.96
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• pp.785-791
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• 2006

The purpose of this study is to clarify the effect of the monomer ratio on properties of the polymer-modified mortars based on styrene and butyl acrylate latexes, and to obtain basic data necessary to develop appropriate latexes for cement modifiers. This paper deals with the effects of monomer ratio on the typical properties of the polymer-modified mortars with styrene and butyl acrylate latexes. The polymer-modified mortars using the styrene and butyl acrylate latexes polymerized with various monomer ratios are prepared with different polymer-cement ratios, and tested for the particle size of polymer latexes, air contents, water-cement ratios, flexural and compressive strengths, water absorption, and chloride-ion penetration. From the test results, the polymer-modified mortars using styrene and butyl acrylate latexes with the mix proportions of synthesis having monomer ratios of 50:50 to 60:40 for the appropriate mix proportions can be recommended for practical applications. Their basic properties are greatly affected by the polymer-cement ratio rather than the monomer ratio, and are improved over un-modified mortar.

• Elastomers and Composites
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• v.45 no.4
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• pp.256-262
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• 2010

Dispersion polymerization of methyl acrylate, ethyl acrylate, butyl acrylate, and glycidyl methacrylate were performed in supercritical $CO_2$ at $80\;^{\circ}C$ and 346 bar. Glycidyl methacrylate linked poly(dimethylsiloxane) (GMS-PDMS) surfactant, which was prepared by linking glycidyl methacrylate to monoglycidyl ether terminated PDMS with amino-propyltriethoxysilane, was used as surfactant for the dispersion polymerization in $CO_2$. The yield of the poly(alkyl acrylate) polymers, synthesized in $CO_2$ medium, decreased as the alkyl tail of the acrylate monomers increased. Poly(glycidyl methacrylate) and poly(methyl acrylate) were produced in bead form whereas poly(ethyl acrylate) and poly(butyl acrylate) were viscous liquid. The poly(glycidyl methacrylate) particles had a number average diameter of 2.45 ${\mu}m$ and monodisperse distribution. The poly(methyl acrylate) had a number average diameter of 0.52 ${\mu}m$ and the particle size distribution was bimodal. The glass transition temperatures ($T_g$) of the poly(glycidyl methacrylate) and the poly(alkyl acrylate) products were 4~9 K higher than the $T_g$ of the corresponding acrylate polymers synthesized in conventional processes.

• Elastomers and Composites
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• v.44 no.2
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• pp.175-181
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• 2009

The solution polymerization was conducted to synthesize pressure sensitive adhesive for polarizer film using acrylic monomers. 2-Ethylhexyl acrylate, butyl acrylate, acrylic acid were used as acrylic monomers, benzoyl peroxide as initiator, ethyl acetate as solvent. The ratio of monomers was 2-ethylhexyl acrylate: butyl acrylate: acrylic acid = 25:50:3.6 reflecting $-40^{\circ}C$ of glass transition temperature in the pressure sensitive adhesive. The amount of initiator was determined as 0.09% to monomer considering wetting power and initial tackiness. The ratio of monomer to solvent was determined as 1:1.7 considering wetting power and transmissivity. The transmissivity of pressure sensitive adhesive increased with decreasing both viscosity and molecular weight due to reducing of refractive index by low entanglement between molecules. In the measurement of pot life, it was found that the storage stability was good at 1:1.7 of monomer: solvent without large change of viscosity during 200 min.

• Journal of Adhesion and Interface
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• v.13 no.2
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• pp.64-72
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• 2012

Vinyl acetate/alkyl acrylate copolymers were prepared by water-born emulsion copolymerization according to the compositional change of vinyl acetate and various alkyl acrylates such as methyl acrylate (MA), ethyl acrylate (EA), and n-butyl acrylate (BA). Ammonium persulfate (APS) was used as an initiator and poly(vinyl alcohol) (PVA) was used as a protective colloid. The significant result was described as follows. The activation energy determined by an isothermal analysis in the temperature region between $100{\sim}200^{\circ}C$ of the copolymer had the order of PVAc/PMA > PVAc/PEA > PVAc/PBA. The peel strengths before and after the plasma treatment were the order of PVAc/PMA > PVAc/PEA > PVAc/PBA.