• Macromolecular Research
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• v.10 no.3
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• pp.140-144
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• 2002

Dispersion polymerization of acrylamide was carried out in the media of methyl alcohol/$H_2O$ mixtures using hydroxypropyl cellulose and ammonium persulfate as steric stabilizer and initiator, respectively. The effects of concentrations of initiator and steric stabilizer, amount of monomer, polymerization temperature, methyl alcohol/$H_2O$ ratio, and purification of monomer and nitrogen purge on the particle size of the latices and molecular weight of the polymers were investigated. The average particle diameter increased with increasing concentration of initiator, water content in methyl alcohol/$H_2O$ media, and polymerization temperature, but decreased with monomer and stabilizer concentrations. The viscosity average molecular weight increased with increasing concentrations of monomer, steric stabilizer, and water content in dispersion media, but decreased with initiator concentration and polymerization temperature. The PAM polymers prepared with the purified monomer and the nitrogen purging before the reaction showed the highest molecular weight.

• Bulletin of the Korean Chemical Society
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• v.27 no.2
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• pp.251-254
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• 2006

The formation of polyaniline (PANI) in the reverse micelles of poly(oxyethylene) nonylphenyl ether, $(NP5, H(CH_2)_9Ph(OC_2H_4)_5OH)$, was investigated by small-angle neutron scattering (SANS). The reverse micellar solution containing initiators in the inner part of reverse micelle was prepared with surfactant (NP5), water, cyclohexane and an initiator (ammonium persulfate (APS)). The core-shell sphere model containing smearing effect reveals that the polymerization occurs on the shell layer of the reverse micelles. Shell thickness averages varied from 48 $\AA$ to 109 $\AA$ with increases of monomer concentration.

• Journal of the Korean Society of Safety
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• v.17 no.4
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• pp.133-139
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• 2002

Core-shell polymers of inorganic/organic pair, which are consisted of both core and shell component, were synthesized by sequential emulsion polymerization using ethyl methacrylate (EMA) as a shell monomer and ammonium persulfate as initiator. We found that $CaCO_3$ core should be prepared by adding 2.0wt% SDBS(sodium dodecyl benzene sulfonate), $CaCO_3$ core/PEMA shell polymerization was carried out on the surface of $CaCO_3$ particle during EMA shell polymerization in the core-shell polymer preparation. The structure of core-shell polymer were investigated by measuring the degree on decomposition of $CaCO_3$ by HCI solution, thermal decomposition of polymer composite on thermogravimetric analyzer, glass transition temperature on differential scanning calorimeter, and morphology using scanning electron microscope.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2007.11a
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• pp.109-110
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• 2007

Pyrrole and DNA can be used for synthesis of conducting nanowires. Protonated pyrrole and negatively charged DNA are absorbed by electrostatic interaction. The level of absorbance is related to pH of pyrrole. Therefore, DNA immobilized and aligned on the 3-aminopropyltrimethoxysi1ane (APTES) modified Si surface. Positive pyrrole monomers was deposited on aligned DNA for the synthesis of nanowire in various pH condition. And polypyrrole nanowires were synthesized by polimerization with ammonium persulfate (APS). These polypyrrole nanowires were measured by AFM, and then we found optimal pH level for the synthesis of nanowires.

• Macromolecular Research
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• v.17 no.8
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• pp.609-615
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• 2009

Two types of nano composite were obtained by in situ chemical method in polyaniline (PANI)/dodecyl-benzenesulfonic acid (DBSA) system depending on the use of either ammonium persulfate (APS) or ferric chloride ($FeCl_3$) as the oxidant. In order to study the difference of the two composites in the surface characteristics, thermal stability, and electric properties, the composite films were studied by transmission electron microscopy (TEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and temperature dependent DC electrical conductivity. The results revealed a large difference in the surface morphology, thermal stability, and the microstructure properties between the two composites, and these differences were considered responsible for the molecular order and conductivity.

• Journal of the Korean Wood Science and Technology
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• v.25 no.3
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• pp.75-82
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• 1997

To improve the quality of coated paper, the continuous research to the coating components and development of alternative latices is required. Recently, amphoteric latex is getting a great concern due to their changable properties of surface charge through controlling pH and some methods have been tried to prepare amphoteric latices. This study was carried out to synthesize amphoteric latex using seeding polymerization method with low concentration emulsifier. Styrene was used as a main monomer in addition to acrylonitrile for a hydrophilic comonomer. acrylic acid for a anionic comonomer and N,N-dimethylaminoethyl methacrylate for a cationic comonomer. Particle size and viscosity of latex were greatly affected by addition of acrylic acid and ammonium persulfate as an initiator. Negative charge of latex in alkali condition was changed to zero to positive charge in around pH 4.

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

• Korean Journal of Metals and Materials
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• v.47 no.2
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• pp.91-98
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• 2009

The titania nanotubular layer for photocatalytic application was synthesized by anodization process in HF solution and the photocatalytic efficiencies of nanotubular film were evaluated by the decomposition rate of aniline blue. In order to facilitate the photocatalytic reaction, the electron acceptors such as potassium bromate, hydrogen peroxide and ammonium persulfate were added to aniline blue solution and the effects of electron acceptors on the dye degradation efficiency were evaluated. The results showed that the photocatalytic efficiency has markedly improved by adding the electron acceptors.

• Journal of Digital Convergence
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• v.17 no.1
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• pp.357-364
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• 2019

This study comparatively analyzed hair damage by hair bleach particles and identified three different bleach particle sizes using a scanning electron microscope (SEM). The powdered bleaching agents made of ammonium persulfate (APS) and potassium persulfate had particle sizes of $131{\mu}m$, $72{\mu}m$ and $48.8{\mu}m$. According to a hair damage test, cuticle lift-up or peeling hardly occurred when small bleach particles were used. In terms of hair color, the hair bleached with larger bleach particles was the darkest, while the hair bleached with small bleach particles was the brightest. The results found that for bleaching agents that are more effective in easing hair damage, those with little particles should be used. In addition, it appears that the selection of particles depending on the degree of hair bleaching would enhance bleaching effects and reduce hair damage. The above process is a way to get great results in selecting a bleaching agent. It is anticipated that hair damage could be reduced during hair bleaching based on the above results.

• Journal of Sensor Science and Technology
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• v.10 no.2
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• pp.125-133
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• 2001

Conducting polymer sensors show high sensitivity when exposed to volatile organic compounds gases at room temperature. The 8 sensor array using by polypyrrole and polyaniline has been fabricated by chemical polymerization for measuring sensing characteristics of VOCs gases. Conducting polymer was polymerized by using distilled pyrrole, aniline as a monomer and ammonium persulfate (APS) as an oxidant and dodecylbenzene sulfonic acid (DBSA) as a dopant. Dedoped film was synthesized by reverse voltage and redoped film was synthesized by using 1-octanesulfonic acid sodium salt as another dopant in electrochemical cell. The sensitivity and reversibility were influenced by doping, dedoping, redoping and thickness for the polypyrrole and polyaniline. We investigated the relation between the structure of conducting polymer and sensitivity of these sensors through the analysis of scanning electron microscope (SEM), scanning probe microscope (SPM) and $\alpha$-step.