• Polymer(Korea)
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• v.38 no.5
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• pp.671-675
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• 2014

Well-defined star shaped and linear block copolymers were synthesized to study the dispersion stability of copper phthalocyanine (CuPc). We synthesized dispersants using (2-dimethylamino) ethyl methacrylate (DMAEMA) and poly(ethylene glycol) methyl ether methacrylate) (PEGMA) by activators generated by electron transfer (AGET) atom transfer radical polymerization (ATRP). pDMAEMA-b-pPEGMA copolymers were characterized by GPC and NMR. Furthermore, we studied the effect of the dispersion stability of copper phthalocyanine by controlling the degree of polymerization of PEGMA as a stabilizing group. The 4-arm star shaped polymeric dispersant showed better dispersion stability of CuPc at $25^{\circ}C$ for 7 days.

• Journal of Radiation Industry
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• v.8 no.1
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• pp.49-52
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• 2014

Kenaf fibers have excellent properties and possess the potential to be outstanding reinforcing fillers in cement. The grafting of poly(ethylene glycol) methacrylate (PEGMA) to the kenaf fibers is important in improving the compatibility between the fibers and the cement. PEGMA was grafted onto kenaf fibers using gamma-ray radiation. The radiation dose ranged from 20 to 60 kGy, and the dose rate was $10kGy\;h^{-1}$. The degree of grafting increased with increased radiation doses. FT-IR analysis revealed an increase in PEGMA content after gamma-ray radiation induced grafting, further evincing the attachment of PEGMA to the kenaf fibers. The mechanical properties of the gamma-ray grafted kenaf fiber/cement composites were superior to those of the ungrafted kenaf fiber/cement specimens.

• Journal of Industrial and Engineering Chemistry
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• v.68
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• pp.42-47
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• 2018

This work reports a facile and effective antibacterial coating for oxide substrates. As a coating material, a random copolymer, abbreviated as poly(TMSMA-r-PEGMA), was synthesized by radical polymerization of 3-(trimethoxysilyl)propyl methacrylate (TMSMA) and poly(ethylene glycol) methyl ether methacrylate (PEGMA). Polymeric self-assembled monolayers of poly(TMSMA-r-PEGMA) were formed on various inorganic oxide substrates, including silicon oxide, titanium dioxide, aluminum oxide, and glass, via the simple dip-coating process. The polymer-coated substrates were characterized by ellipsometry, contact angle measurements, and X-ray photoelectron spectroscopy. The bacterial adhesion on the polymer-coated substrates was completely suppressed compared to that on the uncoated substrates.

• Membrane Journal
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• v.23 no.2
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• pp.112-118
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• 2013

Polyancrylonitrile nanofiber membrane (PAM) was prepared by using the electrospinning method with a solution of polyacrylonitrile (PAN) in DMF. The pore-diameter of PAMs and the number of PAM's layer were controlled for the microfiltration (MF) application. In addition, in order to improve the water-flux, AN-PEGMA copolymers have been synthesized via free radical polymerization with poly (ethylene glycol) methyl ether methacrylate and azobisisobutylronitrile (AIBN), and then PAN/AN-PEGMA nanofiber membranes (PAM/APM) were prepared by electrospinning with a mixture of PAN (9 wt%) and AN-PEGMA (3 wt%) in DMF (88 wt%). The prepared membranes were investigated with FT-IR and E.D.S. It was confirmed through scanning electron microscope (SEM), porometer, and porosity analysis that the porous membrane with a uniform diameter (400~600 nm) and a uniform pore characteristics (0.5~0.4 ${\mu}m$) was prepared. For the MF application, water-flux measurements were investigated and then the result was shown that the water permeability value of PAM/APMs introduced AN-PEGMA copolymers was relatively higher than that of the PVdF commercial membrane. From these results, PAN nanofiber membranes prepared by electrospinning could be utilized as a MF membrane.

• Journal of the Korean Electrochemical Society
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• v.18 no.1
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• pp.1-6
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• 2015

In this study polystyrene derivative, VBCE, having a cyclic carbonate was synthesized by Williamson reaction and polymerized to poly(VBCE) successfully in an usual polymerization conditions. The obtained polymer was blended with PEGMA and the effect of composition on the ionic conductivity was investigated. Interestingly, the ionic conductivity was decreased from $4.2{\times}10^{-5}S\;cm^{-1}$ to $3.93{\times}10^{-6}S\;cm^{-1}$ with the poly(VBCE) contents of 5.8mol%. From the DSC study, it was found that the $T_g$ of the blend was increased from $-50^{\circ}C$ to $-21^{\circ}C$ by the addition of poly(VBCE). Therefore, it is believed that the presence of a polar cyclic carbonate makes polymer matrix harder and it is necessary to design new structures less hindered the mobility of the matrix.

• Journal of Electrochemical Science and Technology
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• v.1 no.1
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• pp.57-62
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• 2010

The lithium ion concentration dependant ionic conductivity and thermal properties of poly(ethylene glycol) methyl ether methacrylate (PEGMA)/acrylonitrile-based copolymer electrolytes with $LiClO_4$ have been studied by differential scanning calorimetry (DSC), linear sweep voltammetry (LSV) and AC complex impedance measurements. In systems with 11 wt% of acrylonitrile all liquid electrolytes were obtained regardless of lithium ion concentration. Complex impedance measurements with stainless steel electrodes give ambient ionic conductivities $8.1\times10^{-6}\sim1.4\times10^{-4}S cm^{-1}$. On the other hand, a hard and soft films at ambient temperature were obtained in copolymer electrolyte system consists of 15 wt% acrylonitrile with 6 : 1 and 3 : 1 of [EO] : [Li] ratio, respectively. DSC measurements indicate the crystalline melting temperature of poly(PEGMA) disappeared completely after addition of $LiClO_4$ in this system due to the complex formation between ethylene oxide (EO) unit and lithium salt. As a result, free standing film with room temperature ionic conductivity of $1.7\times10^{-4}S cm^{-1}$ and high electrochemical stability up to 5.5V was obtained by controlling of acrylonitrile and lithium salt concentration.

• Journal of the Korean Society of Visualization
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• v.12 no.1
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• pp.49-53
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• 2014

In this study, a novel FDR-SPC is first synthesized in this study. The drag reducing functional radical such as PEGMA (Poly(ethylene) glycol methacrylate) has been utilized to participate in the synthesis process of the SPC. The types of the baseline SPC monomers, the molecular weight and the mole fraction of PEGMA were varied in the synthesis process. The resulting SPCs were coated to the substrate plates for the subsequent hydrodynamic test for skin friction measurement. In a low-Reynolds number flow measurement using PIV (Particle Image Velocimeter), a significant reduction in Reynolds stress was observed in a range of specimen, with the maximum drag reduction being 15.9% relative to the smooth surface.

• Journal of Radiation Industry
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• v.6 no.3
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• pp.251-255
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• 2012

Pulp is typically used for paper industry to manufacturing various types of papers. However simply chemical modification makes enable the pulp to a wide range of application in various industrial fields. To bring the polymerization the gamma ray irradiated on the mixture of kenaf and PEGMA in various dose ranges from 20 to 60 kGy. As a results, the graft degree of 20.0% was obtained from 475 g of gamma ray irradiated pulp and PEGMA. After the polymerization, the chemical structure and morphology of the surfaces were examined by Fourier transform infrared spectroscopy, thermogravimetric analysis, and scanning electron microscope. Chemical structure of grafted pulp has significantly growth in carbonyl content with increasing the radiation dose. Also surface morphology was distinctly changed with decreased the degree of roughness and increasing the diameter. These results were explained gamma ray irradiation improve performance of graft polymerization efficiency.

• Macromolecular Research
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• v.17 no.3
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• pp.174-180
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• 2009

Chemical modification of titanium/titanium oxide (Ti/$TiO_2$) substrates has recently gained a great deal of attention because of the applications of Ti/$TiO_2$-based materials to biomedical areas. The reported modification methods generally involve passive coating of Ti/$TiO_2$ substrates with protein-resistant materials, and poly(ethylene glycol) (PEG) has proven advantageous for bestowing a nonbiofouling property on the surface of Ti/$TiO_2$. However, the wider applications of Ti/$TiO_2$ based materials to biomedical areas will require the introduction of biologically active moieties onto Ti/$TiO_2$, in addition to nonbiofouling property. In this work, we therefore utilized surface-initiated polymerization to coat the Ti/$TiO_2$ substrates with polymers presenting the nonbiofouling PEG moiety and subsequently conjugated biologically active compounds to the PEG-presenting, polymeric films. Specifically, a Ti/$TiO_2$ surface was chemically modified to present an initiator for atom transfer radical polymerization, and poly(ethylene glycol) methacrylate (pEGMA) was polymerized from the surface. After activation of hydroxyl groups of poly(pEGMA) (pPEGMA) with N,N'-disuccinimidyl carbonate, biotin, a model compound, was conjugated to the pPEGMA films. The reactions were confirmed by infrared spectroscopy, X-ray photoelectron spectroscopy, contact angle goniometry, and ellipsometry. The biospecific binding of target proteins was also utilized to generate micropatterns of proteins on the Ti/$TiO_2$ surface.

• Macromolecular Research
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• v.17 no.4
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• pp.259-264
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• 2009

Chemical modification of magnetic nanoparticles(MNPs) with functional polymers has recently gained a great deal of attention because of the potential application of MNPs to in vivo and in vitro biotechnology. The potential use of MNPs as capturing agents and sensitive biosensors has been intensively investigated because MNPs exhibit good separation-capability and binding-specificity for biomolecules after suitable surface functionalization processes. In this work, we demonstrate an efficient method for the surface modification of MNPs, by combining surface-initiated polymerization and the subsequent conjugation of the biologically active molecules. The polymeric shells of non-biofouling poly(poly(ethylene glycol) methacrylate)(pPEGMA) were introduced onto the surface of MNPs by surface-initiated, atom transfer radical polymerization(SI-ATRP). With biotin as a model of biologically active compounds, the polymeric shells underwent successful post-functionalization via activation of the polymeric shells and bioconjugation of biotin. The resulting MNP hybrids showed a biospecific binding property for streptavidin and could be separated by magnet capture.