• Carbon letters
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• 제14권2호
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• pp.94-98
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• 2013

Isotropic pitch fibers were stabilized and carbonized for preparing carbon fibers. To optimize the duration and temperature during the stabilization process, a thermogravimetric analysis was conducted. Stabilized fibers were carbonized at 1000, 1500, and $2000^{\circ}C$ in a furnace under a nitrogen atmosphere. An elemental analysis confirmed that the carbon content increased with an increase in the carbonization temperature. Although short graphitic-like layers were observed with carbon fibers heat-treated at 1500 and $2000^{\circ}C$, Raman spectroscopy and X-ray diffraction revealed no significant effect of the carbonization temperature on the crystalline structure of the carbon fibers, indicating the limit of developing an ordered structure of isotropic pitch-based carbon fibers. The electrical conductivity of the carbonized fiber reached $3.9{\times}10^4$ S/m with the carbonization temperature increasing to $2000^{\circ}C$ using a four-point method.

• Journal of the Korean Wood Science and Technology
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• 제23권4호
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• pp.1-9
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• 1995

This study was carried out to experiment the dimensional stabilization of woods of red pine (Pinus densiflora S. et Z.) and sugi(Cryptomeria japonica D. Don) by vacuum impregnation of polyehtylene glycols(PEG) with mo. wt. 200, 400, 600, 1000; polypropylene glycols (PPG) with mo. wt. 425,725 ; PEG-acryloylates, and PPG-acryloylates synthesized, and then by water soaking. The results obtained are as follows: 1. The density of sapwood and heartwood was different from each other in both species. 2. The PEG and PEG-macromers with lower molecular weight by impregnation has increased the density of wood specimens more higher, thereby caused their higher volume expansion, and those with higher molecular weight than 600 has tended to down their density increment. 3. Before and after water soaking, the density decrease of specimen impregnated was high in woods impregnated with simple PEG and PPG, while lower in specimens impregnated with PEG-macromers and PPG-macromers. 4. So PEG-macromer was expected to hold the original dimension of decayed wood for antiques, but it was necessary to develop another penetration method as well as aqueous solvent.

• Macromolecular Research
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• 제17권7호
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• pp.483-490
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• 2009

Stable poly(styrene-co-divinylbenzene) [P(St-co-DVB)] micro spheres with narrow size distribution were synthesized in the presence of 2,2'-azobis(2,4-dimethyl valeronitrile) (V-65) and co-initiator in an acetone/water mixture in the precipitation polymerization at $53^{\circ}C$ for 24 h. Potassium peroxodisulfate (KPS), ammonium peroxodisulfate (APS) and sodium peroxodisulfate (NaPS) were used as co-initiators. The optimum ratio of acetone to water for the formation of a narrow distribution of P(St-co-DVB) particles was 49:11 (g/g). The optimum co-initiator compositions for narrow distribution were 9:1 (g/g) for V-65 to KPS, 11:1 for V-65 to APS and 6:1 for V-65 to NaPS. The yield for these compositions was $54{\sim}57%$ and the largest particle size was obtained with the lowest zeta-potential and CV values. From the XPS measurements, the charge density was increased but the zeta potential decreased with increasing sulfur content, implying that the sulfate group provides the electrostatic stabilization on the particle surface. This suggested that the self-crosslinking between styrene and DVB, the electrostatic stabilization of initiators, and the balanced hydrophobic and hydrophilic properties of the solvents are responsible for the formation of stable P(St-co-DVB) spherical particles with narrow size distribution.

• Macromolecular Research
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• 제17권6호
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• pp.411-416
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• 2009

The color stabilization of antimicrobial blends was studied by using poly(hexamethylene guanidine) phosphate (PHMG) as a highly efficient biocidal and nontoxic agent. The Taguchi method was used to determine the optimum conditions for the blending of PHMG in polypropylene (PP) matrix. To improve the yellowing phenomena, two kinds of stabilizer were used together: tetrakis[methylene(3,5-di-t-butyl-4-hydroxyhydrocinnamate)](IN1010) from phenol and tris(2,4-di-t-butylphenylphosphite) (IF168) from phosphorus. According to blend composition and mixing condition, six factors were chosen, with five levels being set for each factor. The orthogonal array was selected as the most suitable for fabricating the experimental design, L25, with 6 columns and 25 variations. The-smaller-the-better was used as an optimization criterion. The optimum conditions for these parameters were 10 phr for PHMG, 2 phr for IN1010, 1 phr for IF168, 10 min for mixing time, $210^{\circ}C$ for mixing temperature, and 30 rpm for rotation speed. Under these conditions, the yellowness index of the blend was 1.52. The processibility of the blends was investigated by Advanced Rheometric Expansion System (ARES). The blend with 0.5 w% PHMG content, diluted with PP, exhibited an antimicrobial characteristic in the shake flask method.

• 공업화학
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• 제5권3호
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• pp.537-546
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• 1994

고분자로써 개질을 시킨 아스팔트의 물리적 특성은 여러 가지 매개변수에 의존한다. 예를 들어 고분자의 특성, 고분자의 사용량 및 아스팔트의 물성 등에 의하여 좌우된다. 본 연구의 목적은 고분자로써 개질된 아스팔트의 온도 의존성을 고찰하는데 있다. 아스팔트는 연질의 200/300과 경질의 85/100 2가지 종류를 사용하였으며 개질을 위한 고분자는 염화 폴리에틸렌으로 플라스틱 성질을 갖는 Tyrin 2552와 탄성체 성질을 갖는 Tyrin CM0730 2가지 종류를 사용하였다. 온도에 대한 의존성은 아스팔트나 고분자로 개질된 아스팔트의 특성을 결정하는 기본적인 요인 중 하나이다. 따라서 온도의존성은 penetration index(PI)와 penetration-점도수(PVN) 등의 지수에 의하여 결정되어지는데 이들 지수들은 개질된 아스팔트의 penetration과 점도를 측정하여 이론식에 대입하여 계산함으로서 얻었다. 2종류의 아스팔트는 개질을 위한 고분자를 첨가하였을 경우 PI와 PVN이 동시에 증가하였다. 그리고 Plastomer로 개질시킨 아스팔트에 비하여 PI및 PW이 더 큰 값을 나타내었다. 아울러 연질의 아스팔트가 경질의 아스팔트에 비하여 온도 의존성이 더 큰 것으로 나타났다.

• 폴리머
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• 제30권1호
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• pp.35-44
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• 2006

폴리(비닐 알코올)을 콜레스테릴 클로로포메이트 또는 8-콜레스테릴옥시카보닐헵타노일 클로라이드(CH8C)와 반응시킴에 의해 폴리[1-(콜레스테릴옥시카보닐옥시)에틸렌](PCOE)와 폴리[1-콜레스테릴옥시카보닐헵타노일옥시)에틸렌](PCOSE)를 합성함과 동시에 이들의 열 및 광학 특성을 검토하였다. CH8C는 단방성 콜레스테릭 상을 형성하는 반면 PCOE와 PCOSE는 쌍방성 콜레스테릭 상들을 형성하였다. CH8C의 경우와 같이, PCOSE의 광학피치$(\lambda_m)$는 온도가 상승함에 따라 감소하였다. PCOE는 PCOSE와 달리 반사색깔을 나타내지 않았다. 이러한 사실은 콜레스테릴 그룹에 의한 나선의 비틀림력은 콜레스테릴 그룹과 주사슬을 연결하는 스페이서의 길이에 민감하게 의존함을 시사한다 PCOE와 PCOSE가 나타내는 액정 특성들은 폴리(콜레스테릴-$\omega$-아크릴로일옥시알카노에이트들)이 나타내는 액정 특성들과 전혀 다르다. 이러한 결과들은 곁사슬과 주사슬의 화학결합의 양식이 콜레스테릭 상의 형성능, 안정성 그리고 $\lambda_m$의 온도 의존성에 중요한 역할을 함을 시사한다.

• Korea-Australia Rheology Journal
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• 제20권3호
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• pp.109-116
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• 2008

The effect of intermolecular aggregation induced by hydrophobic and electrostatic interactions on shear and elongational flow properties of aqueous acrylic thickener solutions is discussed. Complex shear modulus is determined at frequencies up to $10^4$ rad/s employing oscillatory squeeze flow. Extensional flow behavior is characterized using Capillary Break-up Extensional Rheometry. Aqueous solutions of poly(acrylic acid)(PAA)/poly(vinylpyrrolidone-co-vinylimidazole) (PVP-VI) mixtures exhibit unusual rheological properties described here for the first time. Zero-shear viscosity of the mixtures increases with decreasing pH and can exceed that of the pure polymers in solution by more than two orders of magnitude. This is attributed to the formation of complexes induced by electrostatic interactions in the pH range, where both polymers are oppositely charged. PAA/PVP-VI mixtures are compared to the commercial thickener Sterocoll FD (BASF SE), which is a statistical co-polymer including (meth) acrylic acid and ethylacrylate (EA) forming aggregates in solution due to "sticky" contacts among hydrophobic EA-sequences. PAA/PVP-VI complexes are less compact and more deformable than the hydrophobic Sterocoll FD aggregates. Solutions of PAA/PVP-VI exhibit a higher zero-shear viscosity even at lower molecular weight of the aggregates, but are strongly shear-thinning in contrast to the weakly shear-thinning solutions of Sterocoll FD. The higher ratio of characteristic relaxation times in shear and elongation determined for PAA/PVP-VI compared to Sterocoll FD solutions reflects, that the charge-induced complexes provide a much stronger resistance to extensional flow than the aggregates formed by hydrophobic interactions. This is most likely due to a break-up of the latter in extensional flow, while there is no evidence for a break-up of complexes for PAA/PVP-VI mixtures. These flexible aggregates are more suitable for the stabilization of thin filaments in extensional flows.

• 한국재료학회지
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• 제31권9호
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• pp.502-510
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• 2021

Hierarchically porous carbon materials with high nitrogen functionalities are extensively studied as high-performance supercapacitor electrode materials. In this study, nitrogen-doped porous carbon textile (N-PCT) with hierarchical pore structures is prepared as an electrode material for supercapacitors from a waste cotton T-shirt (WCT). Porous carbon textile (PCT) is first prepared from WCT by two-step heat treatment of stabilization and carbonization. The PCT is then nitrogen-doped with urea at various concentrations. The obtained N-PCT is found to have multi-modal pore structures with a high specific surface area of 1,299 m² g^-1 and large total pore volume of 1.01 cm³ g^-1. The N-PCT-based electrode shows excellent electrochemical performance in a 3-electrode system, such as a specific capacitance of 235 F g^-1 at 1 A g^-1, excellent cycling stability of 100 % at 5 A g^-1 after 1,000 cycles, and a power density of 2,500 W kg^-1 at an energy density of 3.593 Wh kg^-1. Thus, the prepared N-PCT can be used as an electrode material for supercapacitors.

• 한국재료학회지
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• 제10권5호
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• pp.350-353
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• 2000

강유전성 액정 분자 배향을 위해 열방성 고분자 액정물질을 배향막으로 사용하고 그표면 morphology를 AFM(Atomic Forced Microscope)으로 관찰한 결과 잘 배향된 sample cell에서도 microgroove 구조가 나타나지 않았음을 관찰하였다. 잘 배향된 sample cell 23:1의 contrast ratio를 보이면서 memory 효과를 나타내었다. 또한 20V의 AC field로 안정화시키자 전형적인 stripe-shaped 무늬가 나타났다.

• Journal of Microbiology and Biotechnology
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• 제25권8호
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• pp.1291-1298
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• 2015

Five different polymer nanofibers, namely, polyaniline nanofiber (PANI), magnetically separable polyaniline nanofiber (PAMP), magnetically separable DEAE cellulose fiber (DEAE), magnetically separable CM cellulose fiber (CM), and polystyrene nanofiber (PSNF), have been used for the immobilization of lactase (E.C. 3.2.1.23). Except for CM and PSNF, three polymers showed great properties. The catalytic activities (k_cat) of the free, PANI, PAMP, and magnetic DEAE-cellulose were determined to be 4.0, 2.05, 0.59, and 0.042 mM/min·mg protein, respectively. The lactase immobilized on DEAE, PANI, and PAMP showed improved stability and recyclability. PANI- and PAMP-lactase showed only a 0-3% decrease in activity after 3 months of vigorous shaking conditions (200 rpm) and at room temperature (25℃). PANI-, PAMP-, and DEAE-lactase showed a high percentage of conversion (100%, 47%, and 12%) after a 1 h lactose hydrolysis reaction. The residual activities of PANI-, PAMP-, and DEAE-lactase after 10 times of recycling were 98%, 96%, and 97%, respectively.