• Proceedings of the Membrane Society of Korea Conference
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• 1997.06a
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• pp.93-104
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• 1997

The objective of this study is to develop a method to reduce arsenic concentrations in contaminated water. This work is also aimed at increasing the specificity of membrane separation processes. Arsenic in contaminated waters is often present in the form of negatively charged oxyanions. These are relatively small molecules which cannot be separated directly by ultrafiltration. Oxyanions can be captured by polyelectrolytes and separated by ultrafiltration. Results will be presented on the use of two polyelectrolytes; polyethylenimine (PEI) and poly-diallyl dimethyl ammonium chloride (DADMAC) at various feed concentrations. A semi-continuous process utilizing PEI in a circulation loop was tested. The restfits indicate that better than 99.6 % recovery (permeate concentration < 0.001 $\mu$g/L) can be achieved based on an initial arsenic concentration of 300 $\mu$g/L. The results indicate that this treatment method is suitable as a main treatment process for drinking water or a polishing step after arsenic precipitation.

• Macromolecular Research
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• v.11 no.5
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• pp.322-327
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• 2003

Two kinds of mutually cross-linkable copolymers were prepared to be used as humidity-sensing materials. The humidity-sensitive thin films consist of cross-linked polyelectrolytes of the following component: 4-vinylbenzyl dimethyl 2-(dimethylphosphino)ethyl phosphonium chloride (1)/ bis(2-methoxyethyl)itaconate (2)= 3/l, 2/l, 1/1 and 1/2 and 4-vinylbenzyl chloride (3)/ vinylbenzyl tributyl phosphonium chloride (4)= 3/l, 2/l, 1/1 and 1/2. The humidity sensor prepared from the reaction of 1/2= 2/l with 3/4= 2/l showed an average resistance of 723,36.2 and 2.42 ㏀ at 30, 60 and 90%RH, respectively. Temperature dependence, frequency dependence, and response time were measured and the reliability test such as water durability and long-term stability were also estimated.

• Bulletin of the Korean Chemical Society
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• v.22 no.6
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• pp.559-564
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• 2001

A method for calculating the main characteristics of a potentiometric titration curve in a carboxylic ion exchanger has been investigated. The potentiometric titration curves of simple electrolyte and ion exchangers (polyelectrolytes) showed a great difference between them. The acidity parameters of the ion exchangers, the thermodynamic constant (pK0), apparent equilibrium constant (K), and correction for the apparent equilibrium constant (b), were introduced and used to express the characteristics of the carboxylic ion exchanger. A characteristic equation related to the acidity parameters of the ion exchangers systems was derived. A fibrous carboxylic cation exchanger was used and potentiometric titration curves at different concentrations of the supporting electrolyte were obtained . To prove the validity of the characteristic equation, the concentration of the supporting electroyte was varied. In the present study, good agreement between the data points and the fitted curves was found in all the cases. The g (number of moles of alkali to 1 g of ion exchanger) of carboxylic ion exchanger was calculated from the concentration of supporting electrolyte (C), pH of the solution, and degree of neutralization of ion exchanger (x).

• Bulletin of the Korean Chemical Society
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• v.30 no.9
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• pp.2165-2168
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• 2009

• Polymer Science and Technology
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• v.25 no.1
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• pp.28-37
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• 2014

• Journal of Korea Technical Association of The Pulp and Paper Industry
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• v.46 no.1
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• pp.46-55
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• 2014

In this study, we modified the surface of nanofibrillated cellulose (NFC) through LbL (Layer-by-Layer) multilayering process with polyelectrolytes and investigated the effects of the NFC modification on the charge of NFC surface and the dewatering ability of NFC suspension. The multilayering process was done onto NFC fibers using polydiallyldimethylammonium chloride (PDADMAC) and poly-sodium 4-styrene sulfonate (PSS) under different dosage and washing conditions. When the washing was carried out in every adsorption stage, the modified NFC had strong cationic or anionic charge depending on the type of polyelectrolyte in the outermost layer and the dewatering ability was not affected. In the case of no washing treatment or washing in the final adsorption stage, however, the zeta potential of NFC was close to an isoelectric point so that the dewatering ability increased remarkably. Low addition level of polyelectrolytes also showed the similar results. The mixing of NFC suspensions with opposite charge resulted in higher network strength and improved dewatering ability due to the flocculation.

• Membrane Journal
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• v.12 no.4
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• pp.207-215
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• 2002

The hindered diffusion in confined spaces is an important phenomenon to understand in a micro-scale the filtration mechanism determined by the particle motion in membrane pores. Compared to the case of spherical colloids, both the theoretical investigations and the experiments on the hindered diffusion of polyelectrolytes is actually more difficult, due to lots of relevant parameters resulting from the complicated conformational properties of the polyelectrolyte chain. We have successfully performed the Brownian dynamics simulations upon a single polyeiectrolyte confined in a slit-like pore, where a coarse-grained bead-spring model incorporated with Debye-Huckel interaction is properly adopted. For the given sizes of both the polyelectrolyte and the pore width, the hindered diffusion coefficient decreases as the solution ionic concentration decreases. It is evident that a charge effect of the pore wall enhances the hindered diffusion of polyelectrolyte. Simulation results allow us to make sense of the diffusive transport through the micro-pore, which is restricted by the influences of the steric hindrance of polyelectrolytes as well as the electrostatic repulsion between the polyelectrolytes and pore wall.

• Applied Chemistry for Engineering
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• v.5 no.3
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• pp.443-450
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• 1994

Polyelectrolytes of various ionization degrees, which are prepared by neutralization of poly(acrylic acid)(PAA), were crosslinked by ethylane glycol diglycidyl ether(EGDE) in aqueous solution. $C_{gel}$, the minimum polymer concentration at which gelation occurs, was higher than expected. $C_{gel}$ was comparable with that of neutral polymer. This is considered to be due to the size contraction of polyelectrolyte, which comes from ionic strength increase as polymer concentration is increased. $C_{gel}$ is low when molecular weight of the sample becomes high. It reveals that polyelectrolyte is crosslinked in coil form not in extended rod form. This behavior is similar to the crosslinking of neutral polymers. Polyelectrolytes of partially ionized sample generally follow the behavior of fully ionized polyelectrolyte. Polyelectrolyte with added salt was also studied. Considering the pH dependence of EDGE reactivity it was difficult to compare the system which differs in pH significantly.

• Proceedings of the Korea Technical Association of the Pulp and Paper Industry Conference
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• 2006.06a
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• pp.99-103
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• 2006

Use of recycled fibers in papermaking has been increased for economical and environmental reasons. Recycled panels are major liber resources for brown grades and newsprints. Since the recycled fibers have disadvantageous properties as raw materials for papermaking it is of great importance to optimize the use of these recycled fibers. OCC (Old Corrugated Containers) is the major fiber source for linerboards and corrugating mediums that require diverse specification in strength properties. Many studies have been focused to overcome the problems of strength reduction of brown grades when recycled fibers are used as raw materials. The problem of strength loss for papers made from recycled fibers is closely associated with the increased amount of fines in recycled fibers and hornification of fibers. Fines contained in the recycled fiber resources cause problems not only in paper properties but also in process runnability. This shows that the optimal management and proper use of fines in recycling papermaking system are critical to get most benefits of using recycled fibers. In this study some approaches for optimal use of fiber fines in recycled paper mill have been investigated. Stock samples, prepared in the laboratory and obtained from a recycling plant were used. Fractionation of these samples was made using Sweco screen. And the effect of the addition of polyelectrolytes including cationic PAM and PEI on drainage and retention was evaluated. Different methods of polymer addition were compared to find the most effective ways of treating recycled fiber stocks with polyelectrolytes. Addition of polyelectrolytes to the short fiber fraction was most effective in retention and drainage. The influence of the charge and molecular weight of these two polymers has been examined and discussed.

• Analytical Science and Technology
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• v.8 no.4
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• pp.561-568
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• 1995

Two methods, precipitation and ultrafiltration, were applied in order to recover platinum group metals(PGM) by complexing them with water-soluble polyelectrolytes, e.g., polyethyleneimine [PEl], poly(2-vinylpyridine) [2-PVP], poly (4-vinylpyridine) [4-PVP], and poly (styrene sulfonic acid) [PSSA]. In the precipitation method, the PGM-polyelectrolyte complex that was formed by mixing first with polybase, e.g.,4-PVP at pH 1 was precipitated by further mixing with polyacid, e.g., PSSA. However, the recovery of PGM obtained by this method was not quantitative(less than 70%). The "sandwiching" binding between the metal anions and two polyelectrolytes was examined by X-ray photoelectron spectroscopy(XPS). The XPS studies indicated that the PGM atom was bound with the acdic and basic polyelectrolyte via its oxygen and nitrogen atom, respectively. The recovery of PGM using polyelectrolyte was further studied by ultrafiltration methods as follows : The PGM ions, eomplexed at pH 1 with polyelectrolyte, allowed the applicntion of membrane filtration by virtue of the great differences in molecular weights between PGM and other low molecular weight species. By applying this method, Pd and Pt (ca. $10^{-4}M$) were selectively separated almost quantitatively from coexisting metal ions, e.g., $Cu^{2+}$ and $Ni^{2+}$. The EPR spectra and viscosity measurements indicated that these polyelectrlytes were not bound to $Cu^{2+}$ and $Ni^{2+}$ ions at this pH, which provided the basis for selective separation of PGM(Pd, Pt and Rh) from these coexisting ions.