• Applied Chemistry for Engineering
• /
• v.4 no.3
• /
• pp.627-636
• /
• 1993

Anionic acrylic resin utilizing macromer(TBMA-g-MMA) copolymer was synthesized by preparing (TBMA) macromer using anionic living polymerization, followed by graft copolymerization with MMA macromer. To control the anionic site content in graft copolymer, the relative composition((TBMA) macromer/MMA ratio) of the graft copolymer was controlled at 7/3, 10/90, 15/85, 20/80, 30/70, 40/60, 50/50 in weight content. In the course of anionic living polymerization of(TBMA) macromer, broad molecular weight distribution (1.4~1.5) was obtained by using n-butyllithium-diphenyethylene initiatior system at $-78^{\circ}C$. To introduce the double bond at the end of chain in termination step, methacryloyl chloride was reacted after insertion of benzaldehyde as capping material. Moreover, TBMA parts in graft copolymer were hydrolyzed in the presence of p-toluenesulfonic acid catalyst, and neutralization of graft copolymer with triethylamine was granted acrylic resin to anionic site. Molecular weight and molecular weight distribution of(TBMA) macromer were determined by GPC, and the hydrolysis of TBMA with neutralization of acrylic resin were determined by IR and NMR. From water dispersion and stability point of view, stable dispersion state appeared at low molecular weight(TBMA) macromer with a small TBMA content as a result of scrutiny about the relation to TBMA content and branch length for(TBMA) macromer molecular weight in graft copolymer.

• Journal of the Korean Electrochemical Society
• /
• v.12 no.2
• /
• pp.173-180
• /
• 2009

In order to develop a novel polymer electrolyte membrane for direct methanol fuel cell (DMFC), styrene monomer was graft-polymerized into poly(tetrafluoroethylene perfluoropropyl vinyl ether) (PFA) film followed by a sulfonation reaction. The graft polymerization was prepared by the $\Upsilon$-ray radiation-grafting method. Subsequently, sulfonation of the radiation-grafted film was carried out in a chlorosulfonic acid/1,2-dichloroethane (2 v/v%) solution. The chemical, physical, electrochemical and morphological properties of the radiation-grafted membranes (PFA-g-PSSA) were characterized by fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The water uptake, ionic conductivity, and methanol permeability of the PFA-g-PSSA membrane were also measured. The cell performances of MEA prepared with the PFA-g-PSSA membranes were evaluated and the cell resistances were measured by an impedance analyzer. The MEA using PFA-g-PSSA membranes showed superior performance for DMFCs in comparison with the commercial Nafion 112 membrane.

• Clean Technology
• /
• v.19 no.4
• /
• pp.393-400
• /
• 2013

In this study, Polyethylene wax, which was produced in manufacturing process of high density polyethylene was grafted with maleic anhydride (MAH). The influences of reaction parameters on the graft polymerization as well as the effect of hydrolysis of the anhydride functions were investigated. The results show that the grafting degree increased and conversion of maleic anhydride decreased with an increase in MAH monomer content. This means the highest grafting efficiency for the reaction can be met when MAH monomer content is about 15 wt%. DCP (dicumyl peroxide) and DTBP (di-tert-butyl peroxide) have been used as the initiator and the highest yield of grafting was obtained when the initiator content is about 0.5 wt%. However, It can be seen that the gel content values of this polyethylene wax grafted MAH were below 2%. It was also observed that the grafting degree increased with an increase in reaction temperature and the maximum value was reached 2 hours later. Although MAH functions grafted onto polyethylene wax were mainly in the carboxylic acid forms, some anhydride form of MAH appeared in over 5% of grafting degree. As a result of hydrolysis reaction, it was observed that the conversion of anhydride group into carboxylic acid group was reached up to 10%.

• Applied Chemistry for Engineering
• /
• v.9 no.3
• /
• pp.451-456
• /
• 1998

By grafting acrylic acid, fumalic acid and maleic acid onto chitosan, graft copolymers, CsAa, CsFa and CsMa, respectively were prepared for potential uses as flocculants in waste water treatment. When 40 ppm of each grafted chitosan sample was added into the waste water, CsMa showed the best removal rate of COD and suspended solids(SS), followed by CsFa and CsAa and chitosan. The transmittance and removal rate of COD and SS were the highest at pH 5. All grafted chitosan exhibited better performance than chitosan itself, resulting from the amphiphilic property of grafted chitosan copolymer with carboxy groups.

• Polymer(Korea)
• /
• v.24 no.2
• /
• pp.174-181
• /
• 2000

The ACF/PP-g-AN copolymers were synthesized by the irradiational grafting of acrylonitrile onto ACF/PP hybrid fabric. The synthesis of the ACF/PP-g-AN copolymer was evidenced by the band of -C=N absorption peak at 2250 $cm^{-1}$ / and amidoximation was evidenced by the band of -OH and -NH$_2$ peak at 3450 $cm^{-1}$ / on FT-IR spectrum. The optimal time for the uranium ion adsorption equilibrium on ACF/PP-g-AN copolymers was 8 days and the optimal pH was 8. The adsorption capacities of ACF/PP-g-AN copolymers increased according to the content of amidoxime and were not varied even after more than 10 times of regeneration.

• Journal of the Korean Chemical Society
• /
• v.36 no.1
• /
• pp.131-136
• /
• 1992

New graft copolymers were synthesized by grafting 2,2,2-trifluoroethylmethacrylate on polyvinylalcohol in aqueous solution with $Ce^{4+}$ ions as initiator. Surface free energies of copolymers having various grafting percentages were studied by measurements of contact angles for various liquids. As the grafting of perfluoroalkyl group increases, surface free energy of solid decreases. Estimation of critical surface free energy should be accounted for molecular properties because the polar force components of these solids are relatively great. ${\gamma}_c$ was calculated from the plot of ${\gamma}_{si}$ vs ${\Phi}_{sl}$.

• Journal of the Korean Society of Clothing and Textiles
• /
• v.27 no.11
• /
• pp.1252-1259
• /
• 2003

The purpose of this study is to develop multi-functional fabrics by chitosan added on acrylic acid grafted cotton kintted fabrics. Therefore physical properties such as antimicrobial activity, deodorization rate, moisture regain, whiteness, and tensile strength of chitosan added on acrylic acid grafted cotton kintted fabrics were investigated. The results are as follows; According to increased chitosan's concentration, grafting yield was decreased. Therefore thickness of film by treated chitosan added on acrylic acid grafted cotton kintted fabric became thin. FT-IR spectra of chitosan add on acrylic acid grafted cotton kintted fabric clearly showed peaks of COOH and NH$_2$. Antimicrobial activity and deodorization rate of chitosan add on acrylic acid grafted cotton kintted fabrics were increased greatly than untreated. And their durability of laundry were good, Moisture regain of treated fabrics was higher than untreated. Whiteness and tensile strength of treated fabrics were lower than untreated.

• Proceedings of the Membrane Society of Korea Conference
• /
• 1992.10a
• /
• pp.45-46
• /
• 1992

최근들어 많은 연구자들에 의해서 고분자 재료를 이용하여 약물의 방출속도를 조절하며 이를 통해서 장기간에 걸쳐 치료 유효농도이상의 혈중농도를 유지 함으로써 치료효과를 극대화 하려는 연구가 진행되고 있다. 특히 고분자 재료를 이용한 macromolecular drug의 방출조절에 관한 연구가 활발히 진행되고 있다. Macromolercular drug은 인슐린, 알부민등의 단밸질과 유로키나제등의 효소와 같이 약효는 매우 높으나 적절한 투여 수단이 발견되지 않아 투여가 매우 번거로운 단점을 가지고 있다. 이와같은 macromolecular drug의 대부분은 구강을 통해서 투여하는 것은 거의 불가능하며 체내 반감기도 매우 짧아서 절절한 투여방법의 개선이 필요하다. 따라서 본 연구실에서는 macromolecular drug의 투여방법을 개선하고자 다공성 고분자막을 이용하였으며 생체 환경의 변화에 대해서 투과속도가 변화하는 자극감응성 고분자 막을 개발하고저 기질로 사용한 고분자 막의 표면에 기능성 모노머를 그라프트 반응을 통해서 도입하고 이의 이용 가능성을 확인하였다.

• Textile Coloration and Finishing
• /
• v.11 no.3
• /
• pp.41-48
• /
• 1999

The removal of hemoglobin from acrylic acid grafted Nylon fabrics has been investigated. In order to change detergency of Nylon 6 fabric, acrylic acid(AA) were graft copolymerized on Nylon fabric using ammonium persulfate(APS) as a initiator, and then acrylic acid grafted Nylon was treated with NaOH solution. The graft ratio increased linearly with increasing acrylic acid concentration. The graft ratio was the highest when the concentration of APS was 0.05%, and it decreased as the concentration of APS increased. The surface of Nylon fabric became rough due to graft. Moisture regain was increased by graft and alkaline treatment, contact angle was also improved compared with the ungrafted. The hemoglobin was easily solubilized and removed from grafted Nylon fabric, while it was difficult to remove hemoglobin from ungrafted Nylon fabric. The effects of graft on removal of hemoglobin was related with increase of moisture regain and transformation of COOH to COONa by alkaline treatment.

• Textile Coloration and Finishing
• /
• v.6 no.2
• /
• pp.17-23
• /
• 1994

Carboxylic acid group gradient surface where the density of carboxylic acid groups changes gradually along the sample length was prepared. Carboxylic acid group gradient surface was produced by the treatment of low density polyethylene sheet using a corona with gradually increasing power, followed by the grad polymerization of acrylic acid. The prepared gradient surface was characterized by the measurement of water contact angle, Fourier-transform infrared spectroscopy in the attenuated total reflectance mode, and electron spectroscopy for chemical analysis.