• Bulletin of the Korean Chemical Society
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• v.19 no.11
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• pp.1156-1160
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• 1998

Alternating multilayer films of a cationic bipolar amphiphile and an anionic polyelectrolyte were prepared by a self-assembly method based on electrostatic attraction between opposite charges. The bipolar amphiphile contains an azobenzene unit in order to allow for a trans-cis photoisomerization to take place. Optical birefringence or dichroism was induced in the self-assembled film upon linearly polarized light irradiation. This dichroism could be reversibly written and erased by irradiation with light of an appropriate wavelength.

• Journal of Korea Technical Association of The Pulp and Paper Industry
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• v.46 no.6
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• pp.78-86
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• 2014

Since cellulose nanofibrils (CNF) has large specific surface area and high water holding capacity, it is very difficult task to remove water from the CNF suspension. However, dewatering of CNF suspension is a prerequisite of following processes such as mat forming and drying for the application of CNF. In this study, we evaluated the drainage of cellulose fibers suspension under vacuum and pressure conditions depending on the number of grinding passes. Also, the effect of the addition of cationic polyelectrolyte on dewatering ability of CNF suspension was investigated. Regardless of dewatering condition, the total drained water amount as well as the drainage rate were decreased with an increase in the number of grinding passes. Pressure dewatering equipment enables us to prepare wet CNF mat with relatively higher grammage. The cationic polyelectrolytes improved the dewatering ability of CNF suspension by controlling the zeta potential of CNF. The fast drainage was obtained when CNF suspension had around neutral zeta potential.

• Journal of Korea Technical Association of The Pulp and Paper Industry
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• v.43 no.3
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• pp.35-42
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• 2011

In this study, ground calcium carbonate (GCC) was modified by Layer-by-Layer (LbL) multilayering with polyelectrolytes. Cationic polyacrylamide (C-PAM) and poly sodium 4-styrene sulfonate (PSS) were used as cationic and anionic polyelectrolytes to modify GCC. The characteristics of the modified GCC were examined in terms of zeta potential and particle size with the addition level of polyelectrolyte and layer number. The GCC could form an assembly of cationic and anionic polyelectrolytes through consecutive adsorption process. The zeta potential of the modified GCC moved toward the cationicity and reached the plateau with the increase of the addition level of C-PAM. With layering of anionic PSS, the GCC had the negative charge. The particle size was dependent on the zeta potential. It was also observed by optical microscope. As the PSS was in the presence of the outermost layer, the GCC showed the better dispersability. It indicated that the surface charge and particle size can be controlled by adjusting the addition level of polyelectrolyte and the layer number.

• Bulletin of the Korean Chemical Society
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• v.29 no.1
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• pp.104-110
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• 2008

Poly(allylamine) hydrochloride is a weak cationic polyelectrolyte that exhibits different aggregation properties at different solution pH values and aging times. Specifically, after several days aging in a pH 3 buffer, less than 1 mg/mL poly(allylamine) hydrochloride became turbid, and the hydrodynamic radius increased with a single diffusion mode. However, the hydrodynamic radius did not change at high concentrations. The dynamic processes of polymer aggregations at different pH values were verified by a light scattering and zeta-potential apparatus. The major interaction was caused by the capturing of counterions by the polyelectrolyte, which generates electrostatic, hydrophobic and cation-p interactions.

• Macromolecular Research
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• v.13 no.3
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• pp.265-272
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• 2005

Polyelectrolyte membranes for humidity-sensing were fabricated using a layer-by-layer adsorption process based on the spontaneous self-assembly of alternating layers of cationic and anionic polymers on a silanized ITO patterned glass substrate. The substrate is dipped successively into dilute solutions of a polyanion and a polycation. The homopolymers and copoymers of diallyldimethylammonium chloride (DDA), allylamine hydrochloride (AA), 2-[(methacryloyloxy)ethyl]trimethyl ammonium chloride (METAC) and vinylbenzyl tributyl phosphonium chloride(VTBPC) were used as the polycations. In this experiment, it was found that the resistance varied according to the chemical structure of the polycation. The resistance varied from $10^7$ to $10^5$ $\Omega$, as the humidity was increased from 60 (relative humidity) to $95\%$RH, which is the range of RH values required for a dew sensor operating at high humidity.

• Proceedings of the Korea Technical Association of the Pulp and Paper Industry Conference
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• 1999.11b
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• pp.79-83
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• 1999

A cationic demand(CD) is a very useful indication for determining the optimum dosage rate of retention aids to the papermaking stock at the wet end. Polyelectrolyte titration has been most often used to determine a CD. Highly accurate results can be obtained by this method when the ionic strength of sample is low. But this is accompanied by the serious errors when the ionic strength is higher than that corresponding to 20 milli molar(mM) monovalent, 2 mM divalent or 0.2 mM trivalent ions because of no occurrence of the end point of titration. Therefore, it is very difficult or almost impossible for the conventional method to be applied to the industrial suspensions such as papermaking stock and industrial waste water. Then a novel method using chromophoric labeled cationic polymer which can be applicable to the sample with high ionic strength has been developed.

• Journal of Pharmaceutical Investigation
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• v.41 no.2
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• pp.95-102
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• 2011

An amphiphilic cationic branched methoxy poly (ethylene glycol)-branched polyethylenimine - poly(L-phenylalanine) (mPEG-bPEI-pPhe) block copolymer was successfully synthesized by ring-opening polymerization (ROP) of N-carboxyanhydride of L-phenylalanine (Phe-NCA) with mPEG-bPEI for the preparation of more stable polyelectrolyte complex (PEC) included a hydrophobic interaction. mPEG-bPEI was firstly prepared by the coupling of mPEG and bPEI using hexamethylene diisocyanate (HMDI). The structural properties of mPEG-bPEI-pPhe copolymers were confirmed by $^1H$ NMR. The copolymers exhibited a self-assemble behavior in water above critical aggregate concentration (CAC) in the range of 0.01-0.14 g/L. The CAC of copolymers obviously depended on the hydrophobic block content in the copolymers (the value decreased with the increase of the pPhe block content). The cationic copolymers have the ability to form multi-interaction complex (MIC) with bovine serum albumin (BSA) and plasmid DNA through multi-interaction (electrostatic and hydrophobic interaction). The physicochemical characterization of the complex was carried out by the measurement of zeta potential and particle size. Their zeta-potentials were positive (approximately +10 mV) and their sizes decreased with increasing pPhe contents in the copolymers (PPF/BSA wt% ratio = 2). The complex showed good stability at high ionic strength. Therefore, mPEG-bPEI-pPhe block copolymer was considered as a potential material to enhance the stability of complex including biotherapuetic drugs.

• Journal of Environmental Health Sciences
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• v.30 no.3
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• pp.253-258
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• 2004

Synthetic organic polyelectrolytes can be used to condition sludges to enhance their dewaterability. Intermittent aerobic digestion is an useful digestion technology and has many advantages like neutral pH, low installation cost and easiness to operation. The objectives of this study were to investigate the dewaterability of intemittent aerobic digestion sludge and to find the relationship between dewaterability and particle size distribution change under the conditioning of intermittent aerobic digestion sludge by cationic polyelectrolyte. Digested sludge from intermittent aerobic digestion was used and cationic polyacrylamide polymer was added as a conditioner. CST(capillary suction time), TTF(time-to-filtration) were tested as a dewaterability index and the number of particle distribution was analyzed using particle size analyzer. The results indicate that cationic polyelectrolytes is useful to enhance dewaterability of intermittent aerobic digestion sludge. Mean particle diameter was increased as polymer dosage increased and its value was reached up to 100 mm on the condition of optimal cationic polymer dosage. CST and TTF are well correlated with mean particle diameter when the weighting order is 1.7. By the optimal conditioning with cationic polymer, particles in the filtrate are also reduced significantly and this means that conditioning is helpful to main stream by reducing SS loading from return flow.

• Applied Chemistry for Engineering
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• v.9 no.4
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• pp.569-573
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• 1998

A water soluble polymer, polycondensate of 1-butylamine and epichlorohydrin (PBE), was synthesized by condensation of 1-butylamine and epichlorohydrin. The characteristics of PBE were determined by IR spectroscopy, low angle light scattering measurement, and $\zeta$ potential measurement. Its interactions with colloidal bentonite particles in aqueous medium were also studied. The results of the studies are as follows : PBE is a cationic polyelectrolyte carrying tertiary ammonium ions on its backbone. The average molecular weight of PBE is found to be about 1,600. The adsorption of PBE on the colloidal bentonite particles are well described with Langmuir adsorption isotherm. As the amounts of PBE adsorbed on the bentonite particles increase, the $\zeta$ potential of the particles changes its sign from negative to positive. This inversion of charge confirms that PBE is cationic in nature. The adsorption of PBE onto the bentonite particles was found to occur through cation exchange reaction. It has been shown that PBE has flocculation effects on the colloidal suspension of bentonite. It has also enhanced effects of filtrability on the digested sludge.

• Journal of Environmental Science International
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• v.14 no.8
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• pp.723-737
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• 2005

The effects of pH (5, 7 and 9) and ionic strength of different salts on the flocculation characteristics of humic acid by inorganic (alum, polyaluminum chloride (PAC) with degree of neutralization, r=(OH/Al) of 1.7) and organic (cationic polyelectrolyte) coagulants, have been examined using a simple continuous optical technique, coupled with measurements of zeta potential. The results are compared mainly by the mechanisms of its destabilization and subsequent removal. The destabilization and subsequent removal of humic acid by PAC and cationic polyelectrolyte occur by a simple charge neutralization, regardless of pH of the solution. However, the mechanism of those by alum is greatly dependent on pH and coagulant dosage, i.e., both mechanisms of charge neutralization at lower dosages and sweep flocculation at higher dosages at pH 5, by sweep flocculation mechanism at pH 7, and little flocculation because of electrostatic repulsion between negatively charged humic acid and aluminum species at pH 9. The ionic strength also affects those greatly, mainly based on the charge of salts, and so is more evident for the salts of highly charged cationic species, such as $CaCl_2$ and $MgCI_2.$ However, it is found that the salts have no effect on those at the optimum dosage for alum acting by the mechanism of sweep flocculation at pH 7, regardless of their charge.