• Journal of Pharmaceutical Investigation
• /
• v.18 no.2
• /
• pp.83-88
• /
• 1988

We examined effects of crosslinking agents, i.e., ethyleneglycol dimethacrylate (EGD) and butanediol dimethacrylate (BDD) containing ester groups on chloromethylation of crosslinked polystyrene resin matrices. It was proved that the ester group in methylmethacrylate (MMA) accelerates the chloromethylation of the divinylbenzene (DVB)-crosslinked styrene-MMA copolymer. As the MMA content increased in the styrene-MMA copolymers, the chloromethylation was enhanced. Complete chloromethylation was obtained at about 25% MMA content.

• Proceedings of the Korean Environmental Health Society Conference
• /
• 2005.06a
• /
• pp.355-358
• /
• 2005

Nitrate-selective ion exchange resins involving bulky trialkyl amino as functional group were synthesized by the reaction of chloromethylated polystyrene-divinylbenzene copolymer and the corresponding tripropylamine in ethanol. Fundmental properties such as bulk density, water content, effeative diameter, uniformity coefficient, appearance index, exchange capacity and particle size distribution were fully measured. The synthesized resins appeared to be good for nitrate selection.

• Journal of Integrative Natural Science
• /
• v.6 no.3
• /
• pp.151-157
• /
• 2013

The ion exchange resins were synthesized from 1-aza-18-crown-6 macrocyclic ligand attached to styrene (2th petroleum in 4th class hazardous material) divinylbenzene (DVB) copolymer with crosslinks of 1%, 6%, and 15% by substitution reaction. These synthetic resins were confirmed by chlorine content, elementary analysis, surface area, and IR-spectrum. The object of this study was to seperate the metal ion absorbed in reinforcement water fire extinguishing agent. As the results of the effects of pH, equilibrium arrival time, and crosslink of synthetic resin on metal ion adsorption for resin adsorbent, the metal ions were showed high adsorption at pH 3 or over and adsorption equilibrium of metal ions was about 2 hours. In addition, adsorption selectivity for the resin in water was the order of Al (III) > Ni (II) > Sm (III) ions, adsorbability of the metal ions was in the crosslinks order of 1%, 6%, and 15%.

• Journal of Integrative Natural Science
• /
• v.10 no.4
• /
• pp.225-231
• /
• 2017

Cryptand resins were synthesized by mixing 1-aza-18-crown-6 macrocyclic ligand with styrene divinylbenzene copolymer having 1%, 2%, 5%, and 10% crosslink by a substitution reaction. These synthetic resins were confirmed by chlorine content, elementary analysis, SEM, surface area, and IR-spectrum. As the results of the effects of pH, crosslink of synthetic resin, and dielectric constant of a solvent on uranium ion adsorption for resin adsorbent, the uranium ion showed high adsorption at pH 3 or over. Adsorption selectivity for the resin in methanol solvent was the order of uranium ($UO_2{^{2+}}$) > calcium ($Ca^{2+}$) > neodymium ($Nd^{3+}$) ion, adsorbability of the uranium ion was the crosslink in order of 1%, 2%, 5%, and 10% and it was increased with the lower dielectric constant.

• Proceedings of the Polymer Society of Korea Conference
• /
• 2006.10a
• /
• pp.318-318
• /
• 2006

4-Vinylbenzyl maltohexaoside peracetate, 1, was copolymerized with divinylbenzene using the initiator for nitroxide-mediated living radical polymerization, 2, to afford the polystyrene microgel with acetyl maltohexaose, 3. The deacetylation of 3 was achieved by treatment with sodium methoxide in dry 1,4-dioxane to produce the polystyrene microgel with maltohexaose, 4. A good coating property of the polystyrene microgel was combined with an excellent hydrophilic property derived from maltohexaose. In addition, 4 showed the ability to solubilize fullerene in aqueous solution. Therefore, 4 has a potential application as a special coating using functional but incompatible compounds such as fullerene on the surface of various hydrophilic materials.

• Journal of environmental and Sanitary engineering
• /
• v.20 no.4 s.58
• /
• pp.38-44
• /
• 2005

Cryptand resins were synthesized with 1-aza-15-crown-5 macrocyclic ligand attached to styrene divinylbenzene (DVB) copolymer with crosslink of $1\%,\;2\%,\;5\%\;and\;10\%$ by substitution reaction. The synthesis of these resins was confirmed by content of chlorine, element analysis, and IR-spectrum. The effects of pH, time, dielectric constant of solvent and crosslink on adsorption of uranium$(UO_2^{2+})$ ion were investigated. The uranium ion was showed fast adsorption on the resins above pH 3. The optimum equilibrium time for adsorption of metallic ions was about two hours. The adsorption selectivity determined in ethanol was in increasing order uranium$(UO_2^{2+})$ > zinc$(Zn^{2+})$ > samarium$(Sm^{3+})$ ion. The adsorption was in order of $1\%>2\%>5\%>10\%$ crosslink resin and adsorption of resin decreased in proportion to order of dielectric constant of solvents.

• Analytical Science and Technology
• /
• v.8 no.4
• /
• pp.529-534
• /
• 1995

The metal ion selective resins were prepared by surface template polymerization using monooleyl phosphoric acid (1), oleyl methyl phosphoric acid (2) or oleyl ethyl phosphoric acid (3) as an amphiphilic host surfactant. The $Cu^{2+}$-imprinted resins prepared in the presence of $Cu^{2+}$ adsorbed $Cu^{2+}$ much more effectively than did their reference resins. On the other hand, the $Cu^{2+}$-imprinted resins showed much less binding ability to $Zn^{2+}$. The template-dependent selectivity should be ascribed to a favorable placement of the surface-anchored metallophilic groups for multidentate coordination to specific metal ion.

• Membrane Journal
• /
• v.6 no.4
• /
• pp.273-283
• /
• 1996

A cation-exchange membranes were prepared by polystyrene and poly(sodium 4-styrene sulfonate). The degree of crosslinking of polystyrene membranes was controlled by DVB. At the same time, the structure of PS membranes was changed from RO to MF by varying the concentration of PSS in the casting solution. Water flux increased with PS-PSS membranes due to the sulfonate groups, and final membrane cast from the solution containing 5% of DVB and 3% of PSS showed MF structure.

• Macromolecular Research
• /
• v.16 no.1
• /
• pp.62-65
• /
• 2008

The morphology of the $D_2O$-induced reverse micellar structure of an amphiphilic block copolymer of poly( ethylene oxide )-b-poly(propylene oxide )-b-poly( ethylene oxide )($EO_{76}PO_{29}EO_{76}$) was investigated in hydrophobic media by small angle neutron scattering (SANS). Increasing $D_2O$ in the styrene/divinylbenzene solution of $EO_{76}PO_{29}EO_{76}$ led to a change in morphology of the reverse micelles from a short range ordered molecular aggregate to a hexagonally arranged micelle, and further to a spherical micelle.

• Proceedings of the Membrane Society of Korea Conference
• /
• 1995.04a
• /
• pp.28-29
• /
• 1995

분리막의 고유기능인 분리기능 뿐 아니라 에너지의 절약을 위하여 분리막공정의 활용은 화학산업 전반에 걸쳐 급격히 신장되고 있다. 따라서 분리막의 효율적인 이용을 위한 연구가 활발히 진행되고 있으며, 특히 분리막 공정의 활용범위를 제한하고 있는 단점(fouling)에 대한 연구를 중심으로 분리막의 소재개발 및 이미 개발되어 잇는 소재의 변형을 통하여 분리막의 응용 범위를 넓혀가고 있다. 본 실험에서는 새로운 소재를 개발하고, 개발된 소재를 토대로 변형공정 및 분리막제조 공정의 변화를 첨가하여 최종 분리막의 구조를 관찰하였다. 또한 분리막의 성능에 대한 변형 공정의 영향을 조사하였다. 분리막의 소재로써 PS(polystyrene)을 채택하였으며, DVB(divinylbenzene)을 이용하여 UV 중합으로 기공의 조절을 시도하였고, 변형공정으로 sulfonation을 하였다. 또한 고분자 열중합으로 PSS[poly(sodium4-styrnesulfate)] 분리막을 제조하였으며, 변형공정에 따른 분리막 구조의 변화를 관찰하고 규명하였다.