• Journal of Integrative Natural Science
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• v.5 no.2
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• pp.127-130
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• 2012

Polymerization of vinyl monomers is promoted by thianthrene cation radical as a part of our research concerning the reactions of various agents with readily isolable, yet highly reactive species and elucidate the biological activity. Thianthrene cation radical initiated the homopolymerization and copolymerization of styrene and ethyl vinyl ether. The polymerization yields decreased as the concentration of phenylacetylene or diphenylethylene increased. Such polymereization by cationic thianthrene radical could provide some clues for the reaction in living animals. Comments on possible polymerization mechanisms were suggested.

• Bulletin of the Korean Chemical Society
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• v.18 no.12
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• pp.1296-1301
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• 1997

Polymerization of terminal alkynes (phenlacetylene and 4-ethynyltoluene) catalyzed by water soluble rhodium (Ⅰ) complex, RhCl(CO)(TPPTS)2 (TPPTS=m-P(C6H4SO3Na)3) (1) selectively produces cis-transoid polymers at room temperature in homogeneous solution of H2O and MeOH as well as in biphasic solutions of H2O and CHCl3. The rate of polymerization is higher in H2O/MeOH than in H2O/CHCl3. The iridium analog, IrCl(CO)(TPPTS)2 (2) shows catalytic activity for the polymerization of phenylacetylene only at elevated temperature to give trans-polymers. The polymerization rate increases significantly when the trimethylamine N-oxide (Me3NO) was added to the reaction mixtures. The electronic absorption spectra of the cis-transoid polymers show three absorption bands whereas the trasn-polymers show only one absorption band. It seems that the electronic absorption bands depend on the configuration of the polymers.

• Macromolecular Research
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• v.17 no.11
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• pp.919-925
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• 2009

The enzymatic polymerization of 12-hydroxystearic acid (12-HSA) was carried out with Lipase $CA^{(R)}$ in benzene to produce poly(12-hydroxystearate) (PHS) with a low molecular weight. When this polymerization was continued for a long reaction time, the PHS once formed was depolymerized into a cyclic diester, 13,16-dihexyl-1,14-dioxacyclohexacosane-2,15-dione (12-HSAD). Similar polymerization and depolymerization were observed when 12-hydroxyoleic acid (12-HOA) was treated with Lipase $CA^{(R)}$, whereas only polymerization occurred when 12-hydroxydodecanoic acid (12-HDA) was treated in a similar manner. The preferential formation of cyclic diesters for 12-HSA was attributed to the structural requirements due to the bulky n-hexyl side groups stemming from the ring systems.

• Applied Chemistry for Engineering
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• v.8 no.5
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• pp.866-871
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• 1997

The com starch was treated with propylene oxide, 1,2-epoxybutane, glycidyl methacrylate, maleic anhydride, caprolactone, respectively, in order to alter the hydrophilicity and the reactivity of starch. When the starch was not dried, poor reaction was observed except the reaction with propylene oxide or maleic anhydride. The treated starches were grafted with styrene by several different polymerization methods. Solution polymerization and redox polymerization using cerium(IV) ion show poor grafting efficiency and poor yield. Encapsulation of starch with polystyrene by suspension polymerization was difficult due to the hydrophilicity of the starch. Among the examined methods, emulsion polymerization was found to be the suitable way to graft styrene onto starch.

• Journal of Sericultural and Entomological Science
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• v.34 no.1
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• pp.49-56
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• 1992

Treatment of vinyl monomers onto silk fiber modifies the properties of the original silk fiber considerably. This field has been the subject of investigation by many workers using chemical and radiation initiation. Many studies on the reaction conditions, polymerization mechanism, physical properties and practical performances of methacrylamide-treated silk fiber have been continued. However, the polymerization mechanism has not been clearly revealed yet and this remains ambiguously whether the grafting is formed on fiber or not. In general, it has been accepted that free radicals were formed and vinyl monomers were polymerized in silk fibroin by graft polymerization mechanism, while active sties were varied by the types of monomer and initiator as well as by the reaction conditions. On the other hand, there is another argument on polymerization mechanism, in which monomers are polymerized and impregnated in the internal side of the fiber by homopolymerization. Though a large number of analytical methods are used to examine the polymerization mechanism of methacrylamide-treated silk fiber, the results on the basis of thermal analysis are merely reported in this paper. In differential scanning calorimetry (DSC) analysis, the thermal decomposition behaviors of the methacrylamie-treated silk fibers were determined and compared to those of the controlled silk fibers. DSC curves obtained from the methacrylamide-treated silk fibers showed double peaks at around 290$^{\circ}C$ (A peak) and 320$^{\circ}C$ (B peak) which are attributed to the thermal decomposition of the methacrylamide polymer and silk fibroin fiber, respectively. The temperature of A and B peak shifted to higher value with the increase of add-on. Also, the moisture regain of the treated silk fibers increased with add-on.

• Applied Chemistry for Engineering
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• v.10 no.6
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• pp.889-894
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• 1999

Preparation of micron size polymer particles which have desired morphology, size, and structure by emulsion polymerization is very difficult due to coagulation of latex particles and formation of second generation particles. But there are attractive merits such as preparation of structural and functional polymer particles in seeded emulsion polymerization. Seeded emulsion polymerization of n-butyl acrylate(BA) was carried out to investigate the effects of stirring rate, reaction temperature, concentration of initiator, emulsifier, and cross-linking agent on the particle size and size distribution. By the combination of suitable reaction conditions, we succeeded in preparing $0.14{\sim}3.67{\mu}m$ diameter of poly(n-butyl acrylate)(PBA) particles using sequential seeded emulsion polymerization.

• Journal of the Korean Ceramic Society
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• v.44 no.2 s.297
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• pp.71-78
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• 2007

A [TEACOOH]-Montmorillonite intercalations complex obtained from Na-Montmorillonite and 10-Carboxy-n-triethylammonium bromide was used to attempt the polymerization of ${\varepsilon}$-caprolactone between the layer spaces of the intercalations complex to achieve Montmorillonite-Polycaprolactone nanocomposites in which the inorganic material (montmorillonite) is chemically combined with the organic polymer (polycaprolactone). The results of X-ray-, IR-, and TEM-analyses for samples obtained after polymerization showed that a polycondensation reaction was successfully produced. For a more precise investigation of the polymeric reaction products the polymerized products were separated from the silicate layers and analyzed with an IR-spectrometer. A comparison of the results of the IR-analyses of the separated polymer with that of the polymer synthesized by the reaction of ${\varepsilon}$-caprolactone with only the organic cation and without montmorillonite showed that the two obtained polymers are the same compound.

• Journal of the Korean Ceramic Society
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• v.43 no.4 s.287
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• pp.207-212
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• 2006

[ ${\varepsilon}-caprolactam$ ] was polymerized in the layers of the [DEACOOH]-Montmorillonite intercalations complex at high temperatures ranging from 250% to 260% formed from Na-Montmorillonite and 10-Carboxy-n-decyldimethylethylammonium bromide to achieve [DEACOOH]-Polycaprolactam-Montmorillonite, in which an inorganic polymer (montmorillonite) is chemically combined with an organic polymer (polycaprolactam). The results of X-ray and IR analyses for the samples obtained after polymerization showed that the polymerization reaction was successfully accomplished. For the purpose of studying the polymeric reaction product more precisely, the polymerized product was separated from the silicate layers and analyzed with an X-ray diffractometer and an IR-spectrometer. A comparison of the results of the X-ray and IR analyses of the separated polymer and the polymer that was synthesized by the reaction of ${\varepsilon}-caprolactam$ solely with the organic cation without montmorillonite showed that the obtained both polymers are identical compounds.

• Applied Chemistry for Engineering
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• v.16 no.5
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• pp.684-688
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• 2005

Aniline was polymerized in various protonic acid (HF, HC1, HBr, HI, $H_2SO_4$) aqueous solutions with different acidity. During the reaction, the dimer formation and the reaction rate were examined as functions of acidity (pH) and the size of counter ions. Open-circuit potential measurements were carried out to investigate the effect of protonic acid on the reaction rate. The results showed that polymerization rate in HF aqueous solution was very slow and polymerization did not occur in HI aqueous solution. These results were explained in terms of acidity and power of oxidation. The ratio of formation of dimers varied with the kind of protonic acid, and the results were explained with the nucleophilicity, solvation effect, and mobility of counter ions.

• Applied Chemistry for Engineering
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• v.31 no.4
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• pp.383-389
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• 2020

Mesoporous silica solid catalysts modified with sulfonic acid were prepared for cationic ring-opening polymerization of octamethylcyclotetrasiloxane (D₄). Two sets of MCM-41 (1.7 and 2.8 nm) and SBA-15 (8.1 and 15.9 nm) with different pore sizes were used as catalyst supports. The surface of silica materials was modified with (3-mercaptopropyl)trimethoxysilane by silylation reaction and oxidized to sulfonic acid. The structures of the prepared catalysts were examined by X-ray diffraction and nitrogen adsorption-desorption. The pore size, specific surface area, and pore volume of the modified solid catalysts decreased slightly. In addition, the modification of the sulfonic acid on the silica surface was confirmed by using infrared spectroscopy and nuclear magnetic resonance spectroscopy. To observe the effect of the particle size on the catalytic activity, it was observed with a scanning electron microscope. The catalysts were used to synthesize PDMS through a ring-opening polymerization of D₄, and the conversion and polymerization rate of the polymerization reaction depended on the pore size, specific surface area, particle size, and particle agglomeration of the catalysts. In order for the polymerization rate, the catalyst prepared with SBA-15 of 8.1 nm pore size had the fastest reaction rate and showed the best catalytic activity.