• Proceedings of the Korean Fiber Society Conference
• /
• 2001.10a
• /
• pp.368-370
• /
• 2001

폴리비닐알코올(poly(vinyl alcohol) (PVA))은 구조적인 단량체인 비닐알코올의 호변 이성질화 때문에 직접 중합에 의해서는 얻을 수 없으며, 아세트산 비닐 (vinyl acetate (VAc))이나 피발산 비닐 (vinyl pivalate (VPi))같은 비닐에스테르 계열 단량체를 사용하여 중합과 비누화 반응을 거쳐 제조되고 비누화 반응에서 모든 측쇄기가 효과적으로 제거되는 히드록시기 함유 선형 결정성 고분자이다[1-4]. (중략)

• Polymer(Korea)
• /
• v.29 no.3
• /
• pp.304-307
• /
• 2005

The acid-catalyzed hydrolysis reaction of poly(vinyl acetate) (PVAc) in water/acetic acid solution at $35^{circ}C$ was studied at two different solvent compositions. The mole fractions of vinyl acetate (Vac) and vinyl alcohol (VA) during the course of the reaction were determined by NMR, and the equilibrium constant $K_{eq}$ of the reaction was determined using the molar ratio of VAc to VA at the chemical equilibrium. $K_{eq}$ was 0.75 (${\pm}0.01$) when the VAc mole faction at the equilibrium was 0.78 (${\pm}0.01$) and it was 0.69 (${\pm}0.01$) when the VAc mole fraction was 0.57 (${\pm}$0.02). The reaction was found to be a pseudo 1-st order reaction with the rate coefficient at $3.4{\times}10^{-6}/sec$.

• Polymer(Korea)
• /
• v.35 no.5
• /
• pp.390-394
• /
• 2011

Effects of silver nanoparticles on the polymerization rate and morphology of poly(vinyl acetate) (PVAc)/silver microspheres prepared by suspension polymerization of VAc were investigated. Scanning electron microscopy, transmission electron microscopy, X-ray diffraction and atomic absorption spectrometry were used to characterize the morphology and properties of the PVAc/silver microspheres. Due to the change of hydrophilicity of silver nanoparticles, appearance of the microspheres having golf ball-like convave surfaces was observed. Under controlled concentration of surfactant, PVAc/silver microspheres with various hollow structures were synthesized. In the case of silver nanoparticles modified by surfactant, the polymerization rate increased slightly. PVAc/silver microspheres with a conversion up to 80% were prepared via suspension polymerization.

• Proceedings of the Korea Society for Energy Engineering kosee Conference
• /
• 2010.04a
• /
• pp.199-199
• /
• 2010

Polymeric membranes have been widely used to separate gas mixtures, such as $O_2/N_2,\;CO_2/CH_4,\;CO_2/N_2$, and olefin/paraffin. The permeation selectivity is the ratio between composition ratio at the permeate side and composition ratio at the feed side. In addition, the permeation selectivity is a product of solubility selectivity and diffusivity selectivity. We present a novel idea and describe its experimental result, which was achieved by preparing polymer gel films that included a room temperature ionic liquid (RTIL) in a polymer matrix. It is known that $CO_2$ can dissolve easily in imidazolium-based RTILs. We prepared polymer-ionic liquid gel films using an ionic liquid, 1-ethyl-3-methylimidazolium acetate ([emim] acetate, C-tri) and a host polymer, poly (vinyl acetate) (PVAc, Aldrich).

• Journal of the Korean Graphic Arts Communication Society
• /
• v.16 no.2
• /
• pp.61-74
• /
• 1998

Some photopolymer, poly(vinyl cinnamoyl acetate)(PVCiA) was synthesized by esterification of polymer(vinyl alcohol)(PVA) with monochloroacetic acid, followed by reaction poly(vinyl monochloroacetate)(PVAhA) and potassium cinnamate. When esterification of PVA with monochloroacetic acid was reacted in the dimethyl sulfoxide(DMSO), in the synthesis of PVChA, it is very good yield and the successive cinnamoyl acetoxyl esterification of PVCiA can be successfully synthesized. But PVCiA is low photosensitive polymer if net added photosensitizing dyes. Here, we synthesized photosensitizing dyes.

• Proceedings of the Korean Fiber Society Conference
• /
• 2003.10b
• /
• pp.52-54
• /
• 2003

Poly(vinyl alcohol) (PVA) obtained by the saponification of poly(vinyl ester) is a linear semicrystalline polymer; these polymers have been widely used as fibers for clothes and industries, binders, films, membranes, medicines for drug delivery system, and cancer cell-killing embolic materials. PVA fibers have high tensile and compressive strength, tensile modulus, and abrasion resistance because of the highest crystalline lattice modulus. (omitted)

• Macromolecular Research
• /
• v.14 no.1
• /
• pp.59-65
• /
• 2006

We report a new approach to fabricate electrospun polymer nonwoven mats with porous surface morphology by varying the collector temperature during electrospinning. Polymers such as poly(L-lactide) (PLLA), polystyrene (PS), and poly(vinyl acetate) (PVAc) were dissolved in volatile solvents, namely methylene chloride (Me) and tetrahydrofuran (THF), and subjected to electrospinning. The temperature of the collector in the electrospinning device was varied by a heating system. The resulting nonwoven mats were characterized by using scanning electron microscopy (SEM), field emission SEM (FESEM), and atomic force microscopy (AFM). We observed that the surface morphology, porous structure, and the properties such as pore size, depth, shape, and distribution of the nonwoven mats were greatly influenced by the collector temperature.

• Advances in concrete construction
• /
• v.11 no.4
• /
• pp.323-333
• /
• 2021

The main objective of this study is to characterize and evaluate the hydrophobic performance of polymer-based water-repellent coatings on cementitious mortar surfaces. Different concentrations of poly(vinyl acetate) (PVAc) and poly(1,4-butylene adipate) (PBA) were prepared in the laboratory and their applicability and performance was tested experimentally by water absorption test and analysis of surface contact angles of cementitious mortar specimens. According to the results of this study, it can be stated that incorporation of nano polymer particles on the surface of cementitious mortar specimens can enhance contact angles and reduce water absorption by increasing hydrophobicity. However, a dosage limit exists for polymer materials in coating, and observed hydrophobic improvements decreases when polymer dosage reached beyond the limit. Additionally, it is observed that water absorption of polymer coated cementitious mortars is closely related with the results of surface contact angle.

• Proceedings of the Korean Fiber Society Conference
• /
• 1998.04a
• /
• pp.135-139
• /
• 1998

Poly(vinyl acetate) (PVAc) from which atactic poly(vinyl alcohol) (PVA) is derived, is always noncrystalline. This was attributed to the irregular steric arrangement of the acetyl groups in PVAc. However, the X-ray diffraction patterns of atactic PVA, a derivative of PVAc, were found to show distinct crystallinity, and to give an identity period of 2,52 ${\AA}$ along the fiber axis, despite the expectation of an irregular arrangement of the hydroxyl groups in atactic PVA, in the same manner as that of the acetyl groups in PVAc.(omitted)

• Membrane Journal
• /
• v.27 no.2
• /
• pp.147-153
• /
• 2017

In this study, we investigated permeation properties of single gas ($N_2$, $O_2$, $CO_2$) through membranes composed of poly(ethylene oxide) (PEO) and poly(ethylene-co-vinyl acetate) (EVA) blend. The prepared membranes showed no new absorbance peaks, which indicate the physical blending of PEO and EVA by FT-IR analysis. SEM observation showed that the crystalline phase of PEO decreased with increasing EVA content in the PEO/EVA mixed matrix. DSC analysis showed that the crystallinity of the PEO/EVA blend membrane decreased with increasing EVA content. Gas permeation experiment was performed with various feed pressure (4~8 bar). The permeability increased in the following order: $N_2$ < $O_2$ < $CO_2$. The permeability of $CO_2$ in PEO/EVA blend membranes were increased with increasing feed pressure, However, the permeability of $N_2$ and $O_2$ were independent of feed pressure. On the other hand, the permeability of all the gases in PEO/EVA blend membranes increased with increasing amorphous EVA content in semi-crystalline PEO. In particular, the blend membrane with 40 wt% EVA showed $CO_2$ permeability of 64 Barrer and $CO_2/N_2$ ideal selectivity of 61.5. The high $CO_2$ permeability and $CO_2/N_2$ ideal selectivity are attributed to strong affinity between the polar ether groups of PEO or the polar ester groups of EVA and polar $CO_2$.