• Journal of the Korean Applied Science and Technology
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• v.4 no.1
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• pp.73-75
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• 1987

Linear alkylbenzene sulfonate (LAS) from the mixture of anionic and nonionic detergents (containing amide type and alkylphenoxy polyethanol type) is identified by Fourier transform infrared spectrometer, separated using physical properties (solubility) and determined by nuclear magnetic resonance spectroscopy.

• Bulletin of the Korean Chemical Society
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• v.22 no.4
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• pp.375-378
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• 2001

The palladium catalyzed dehalogenative homocoupling of haloarylsulfonates under reductive conditions has proceeded selectively depending on the type of the halogen. Thus, an iodo or a bromo leaving group of haloarylsulfonates was homocoupled to gi ve symmetrical biaryls in good yields with the sulfonate group intact, whereas a chloro leaving group gave no reaction under the conditions used. When the more reactive nickel catalyst was employed instead of the palladium catalyst in the reaction, both dehalogenative and desulfonative homocouplings of haloarylsulfonates occurred regardless of the type of the halogen used.

• Bulletin of the Korean Chemical Society
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• v.14 no.5
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• pp.614-618
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• 1993

The photoacid generation efficiency of four N-hydroxyphthalimide sulfonate derivatives was studied by photo-crosslinking reaction of poly(glycidyl methacrylate) in solid film state. The relative photoacid generation efficiency was increased in the order of N-hydroxyphthalimide methanesulfonate > -toluenesulfonate > -nitrobenzenesulfonate > -dinitrobenzensulfonate, and the reaction was efficiently sensitized by benzophenone suggesting that this photoreactions is likely to proceed through its triplet excited state.

• Applied Chemistry for Engineering
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• v.21 no.1
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• pp.93-97
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• 2010

Polyaniline doped with ionic liquid (1,3-dimethylimidazolium methylsulfate, I-DMS) soluble in polar solvents (NMP, DMSO, DMF, m-cresol etc.) were synthesized by nucleophilic addition. Solubilities of PAN/I-DMS powder in polar solvents were observed in the range of 3~6 wt%/vol., respectively. The electrical conductivities of PAN/I-DMS films appeared in the range of $10^{-2}{\sim}7S/cm$. Polyaniline doped with I-DMS (PAN/I-DMS) showed improved thermal stability and conductivity compared to that of HCl doped polyaniline (PAN/HCl) and dimethylsulfate (DMS) doped polyaniline (PAN/DMS) upon heat treatment at $160^{\circ}C$. These improved conductivity and solubility in organic polar solvents was explained with the interactions between the polar sulfonate group and polar solvents.

• Korean Chemical Engineering Research
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• v.50 no.4
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• pp.614-620
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• 2012

Polyurethane prepolymers were prepared from poly (carbonate diol), isophrone diisocyanate and dimethylol propionic acid. Then, aniline terminated waterborne polyurethane dispersion (ATPUD) was synthesized by capping the NCO group of the prepolymer with aniline monomer. Subsequently, ATPUD and waterborne polyurethane dispersion (PUD), respectively, were blended with conducting polymer, poly (3,4-ethylenedioxythiophene)/polystyrene sulfonate [PEDOT/PSS], to yield antistatic coating solutions, and the mixture was coated on the polycarbonate substrates. At adequate addition amounts of PEDOT/PSS less than or equal to 2.5 g, the surface resistances ($1.0{\times}10^{11}{\sim}2.5{\times}10^8{\Omega}/cm^2$) of coating films from ATPUD showed better electronic conductivities than those ($5.0{\times}10^{11}{\sim}6.3{\times}10^9{\Omega}/cm^2$) from PUD. However, at excess amount of PEDOT/PSS of 3.0 g, the surface resistance from ATPUD showed similar electronic conductivity with that from PUD.

• Polymer(Korea)
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• v.39 no.3
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• pp.468-474
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• 2015

Electrically conductive polymer nanocomposites were prepared by the inclusion of graphene-based nanofillers. Graphene oxide (GO) and reduced graphene oxide wrapped by poly(styrene sulfonate) (PSS-RGO) were used as nanofillers to make good dispersion with the aqueous dispersion of polystyrene (PS) particles. GO sheets were synthesized by the modified Hummers' method from graphite, and PSS-RGO sheets were prepared by the reduction of GO-dispersed PSS solution with hydrazine monohydrate. Morphology and properties of PS/GO and PS/PSS-RGO nanocomposites via latex technology were investigated. Both nanofillers showed well dispersed morphology in PS matrix. Rheological and electrical percolation thresholds were 0.28 and 0.51 wt% for GO, and 0.50 and 1.01 wt% for PSS-RGO respectively. It is speculated that PS/GO nanocomposites showed better conductivity than PS/PSS-RGO counterparts due to the partial recovery of GO by thermal reduction during molding.

• Journal of the Korean Chemical Society
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• v.29 no.4
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• pp.335-340
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• 1985

The crystal structure of ethylenediammonium bis (p-methylbenzenesulfonate) monohydrate, $C_2H_{10}N_{22}^{+2}{\cdot}(C_7O_3H_7S^-){\cdot}H_2O$ has been determined by X-ray diffraction techniques. The space group is P21, in 2 unit cell with a = 12.649 (2) ${\AA}$, b = 7.727 (1) ${\AA}$, c = 11.295 (2) ${\AA}$, ${\beta}$ =111.8(1)$^{\circ}$, and z = 2. The structure was solved by direct methods and refined to R = 0.060 for 1134 reflections measured with Mo-K${\alpha}$ radiation. Two p-methylbenzenesulfonates, fragment A and B, from a pair through the hydrogen bonds to the ethylenediammonium ion. The sulfonate group in the fragment B are disordered. There are six unique hydrogen bonds, of which four are between the ethylenediammonium ion and the sulfonate groups and remaining two involve the water molecule.

• Analytical Science and Technology
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• v.6 no.4
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• pp.405-409
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• 1993

Spectrophotometric assay for memantine HCl was developed by using sodium 1-(4-methoxypheyl) cinnamonitrile-2-sulfonate (MPCN) as an UV labelling reagent. The optimum derivatizing condition was obtained by incubation for 30 min at pH 5.0 in the presence of 20-fold molar excess of the labelling reagent. The absorbance of reaction product was measured at 324.5 nm and detection limit was $0.43{\mu}g/ml$. A linear range was $5.0{\times}10^{-6}{\sim}6.5{\times}10^{-5}M$ of memantine HCl. The linear regression analysis of absorbance at various drug concentration was r=0.9998 (n=6). When applied to memantine HCl ampule and tablet, it gave the mean contents of $100.08{\pm}0.72%$ and $99.75{\pm}0.77%$, respectively.

• Journal of the Korean Electrochemical Society
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• v.19 no.4
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• pp.129-133
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• 2016

In this study, a polymer-carbon composite material is prepared for environmental-friendly organic anode. On poly(styrenesulfonate)(PSS)-carbon composite anode, the carbon is coated by PSS as a core-shell structure and the PSS-carbon composite anode has $524mAh\;g^{-1}$ theoretical capacity with <0.6V voltage. Moreover, the PSS-carbon composite anode shows $519.6mAh\;g^{-1}$, $461.2mAh\;g^{-1}$, $411.8mAh\;g^{-1}$ and $315.9mAh\;g^{-1}$ discharge capacities at 0.1, 0.5, 1 and 10 C, respectively, and stable cycle performance up to 30 cycles. The PSS-carbon composite anode, containing polystyrene and sulfonate functional groups, is suitable for high electrochemical properties organic rechargeable battery.

• Applied Chemistry for Engineering
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• v.7 no.5
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• pp.843-848
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• 1996

Porous resin beads of Poly(styrene-co-divinylbenzene) have been prepared by suspension polymerization. The bead could be made porous in the region above 30wt% of the crosslinking agent(divinylbenzene ) and the porogenic agent(toluene), respectively. The specific surface area of porous beads increased with increasing the concentrations of divinylbenzene and toluene. The specific surface area of the porous resin bead decreased, when sulfonated with concentrated sulfuric acid. The catalytic activity of sulfonated resin catalyses increased with increasing the degree of crosslinking in the liquid-phase reesterification of ethyl acetate with 1-propanol. The adsorbed quantity of sodium dodecylbenzene sulfonate in an aqueous solution also increased with increasing surface area of porous resins.