• Carbon letters
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• 제11권3호
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• pp.176-183
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• 2010

PAN precursor fibers were produced via wet-spinning process, and effects of polymerization and spinning processes, especially the stretching process, were investigated on mechanical properties and micro-morphologies of precursor fibers. An increase in molecular weight, dope solid and densification and a decrease in surface defects were possible by controlling polymerization temperature, the number of heating rollers for densification and the jet stretch ratio, which improved the mechanical properties of precursor fibers. The curves for strength, modulus, tensile power and diameter as a function of stretch ratio can be divided into three stages: steady change area, little change area and sudden change area. With the increase of stretch ratio, the fiber diameter became smaller, the degree of crystallization increased and the structure of precursor fibers became compact and homogeneous, which resulted in the increase of strength, modulus and tensile power of precursor fibers. Empirical relationship between fiber strength and stretch ratio was studied by using the sub-cluster statistical theory. It was successfully predicted when the strengths were 0.8 GPa and 1.0 GPa under a certain technical condition, the corresponding stretch ratio of the fiber were 11.16 and 12.83 respectively.

• 센서학회지
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• 제27권5호
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• pp.345-351
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• 2018

We employed an unprecedented technique to synthesize porous $WO_3@SnO_2$ nanofibers exhibiting core-shell and fiber-in-tube configurations. Firstly, 2-methylimidazole was uniformly incorporated in as-spun nanofibers containing ammonium metatungstate hydrate and the sacrificial polymer (polyacrylonitrile). Secondly, the 2-methylimidazole on the surfaces of nanofibers was complexed with tin(II) chloride ($SnCl_2$) via simple impregnation of the as-spun nanofibers in ethanol containing tin(II) chloride dihydrate ($SnCl_2{\cdot}2H_2O$). The presence of vacant p-orbitals in tin (Sn) and the nucleophilic nitrogen on the imidazole ring allowed for the reaction between $SnCl_2$ and 2-methylimidazole, forming adducts on the surfaces of the as-spun nanofibers. The calcination of these nanofibers resulted in porous $WO_3@SnO_2$ nanofibers with a higher surface area ($55.3m^2{\cdot}g^{-1}$) and a better response to 1-5 ppm of acetone than pristine $SnO_2$ NFs synthesized using a similar method. An improved response to acetone was achieved upon functionalization of the $WO_3@SnO_2$ nanofibers with catalytic palladium nanoparticles. This work demonstrates the potential application of $WO_3@SnO_2$ nanofibers as sensing layers for chemiresistive sensory devices for the detection of acetone in exhaled breath.

• 멤브레인
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• 제11권1호
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• pp.14-21
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• 2001

막오염을 줄이기 위해 고빈도 역충격 시스템을 적용한 새로운 분리막 모듈을 연구하였다. 폴리아크릴로니트릴(Polyacrilonitrile) 재질의 외경 1.4mm, 내경 0.9mm, 분획분자량 50,000인 한외여과막과 라텍스(latex)용액을 사용하여 실험하였다. 역충격을 중공사막에 적용했을 때 제안된 모델식에 의한 이론치와 실험치를 비교 분석하였고, 역충격을 적용했을 때와 하지 않았을 때의 경우를 비교하였다. 이론치를 계산하기 위해 비저항 계수(specific cake resistance), 케익성장시간상수(time constant for cake growth), 확산계수(diffusion coefficient), 그리고 4가지 오염모델의 속도상수를 구하였다. 고빈도의 역충격을 가한 모듈의 투과율은 역충격이 없을 때의 투과율보다 약 40∼120%가 증가하였고 모델을 이용한 예상값과 1∼14% 내의 오차 범위를 나타냈다. 최적 역충격 세기는 20∼40%의 범위에서 20%였고 최적 역충격 빈도수는 0.67∼3Hz 범위에서 2Hz로 나타났다.

• Carbon letters
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• 제12권4호
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• pp.236-242
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• 2011

The oxyfluorination effects of activated carbon nanofibers (OFACFs) were investigated for $CO_2$ storage. Electrospun CFs were prepared from a polyacrylonitrile/N,N-dimethylformamide solution via electrospinning and heat treatment. The electrospun CFs were chemically activated in order to generate the pore structure, and then oxyfluorination was used to modify the surface. The samples were labeled CF (electrospun CF), ACF (activated CF), OFACF-1 ($O_2:F_2$ = 7:3), OFACF-2 ($O_2:F_2$ = 5:5) and OFACF-3 ($O_2:F_2$ = 3:7). The functional group of OFACFs was investigated using X-ray photoelectron spectroscopy analysis. The C-F bonds formed on surface of ACFs. The intensities of the C-O peaks increased after oxyfluorination and increased the oxygen content in the reaction gas. The specific surface area, pore volume and pore size of OFACFs were calculated by the Brunauer-Emmett-Teller and density functional theory equation. Through the $N_2$ adsorption isotherm, the specific surface area and pore volume slightly decreased as a result of oxyfluorination treatment. Nevertheless, the $CO_2$ adsorption efficiency of oxyfluorinated ACF improved around 16 wt% due to the semi-ionic interaction effect of surface modificated oxygen functional groups and $CO_2$ molecules.

• 멤브레인
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• 제28권4호
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• pp.279-285
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• 2018

이소프로필알코올/물 혼합물은 가교된 폴리비닐알코올 복합막을 이용하여 투과특성평을 알아보았다. 검화도가 다른 3종 PVA를 이용하여 고분자의 농도와 GA 농도에 따라서 투과특성을 확인하였다. 복합막은 PVA 용액을 PAN 지지체 위에 캐스팅한 후, 열가교를 통해 제조하였다. PVA 농도가 증가할수록 투과도는 감소하지만 선택도는 증가하는 것을 확인하였다. PVA-3이 7 wt% 농도로 코팅된 복합막에서 $209g/m^2h$의 투과도를 가지고, 100 이상의 선택도를 가지는 것을 확인하였다. 침지형 분리막을 제조하여 feed tank 온도와 feed 용액의 IPA 농도에 따라서 투과실험을 확인하였다. 또한 IPA 수용액에 농축실험을 지속적으로 한 결과, 60시간 후에 IPA의 농도가 99%까지 증가하는 것을 확인하였다.

• Carbon letters
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• 제11권1호
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• pp.22-27
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• 2010

The precipitation polymerization of acrylonitrile (AN) was carried out in a mixture solution of dimethyl sulfoxide (DMSO) and water at $50{\sim}65^{\circ}C$ using ${\alpha},{\alpha}'$-azobisisobutyronitrile (AIBN) as an initiator. The increased molecular weight polyacrylonitrile (PAN) was prepared with increasing the $H_2O$/DMSO ratio from 10/90 to 80/20. The viscosity average molecular weight of $H_2O$/DMSO solvent was 4.4 times larger than that of $H_2O$/DMF solvent, and precipitation polymerization was accelerlated due to the far decreased chain transfer effect of DMSO. Based on the experimental results, the increased PAN molecular weight was regarded as the summation of two mechanisms: i) particle-particle aggregation and ii) particle-radical attachment. The theoretical equation derived from the mechanisms was well coincided with the experimental results showing the linear relationship between the viscosity average molecular weight and the H2O/DMSO ratio.

• 폴리머
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• 제26권4호
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• pp.468-476
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• 2002

순수한 PAN 섬유의 예비산화와 가수분해의 과정을 통하여 제조된 oxy-PAN은 염기와 산용액에 담그었을 때 신장과 수축 거동을 보임이 알려져 있다. 본 연구에서는, 염기 (NaOH) 용매에서 약 30%의 신장과 산 (HCl) 용매에서 30∼50%의 수축 거동을 관찰하였다. 기계적 특성에 대한 실험에서, oxy-PAN 섬유가 수축되었을 때 향상된 기계적 특성을 나타내었다. 이러한 거동과 기계적 특성은 인체의 근육과 선형 구동체의 그것들과 유사하였다. NaOH와 HCl 용액에서 oxy-PAN 섬유의 길이가 변화하는 중요한 요인으로는 친수화 또는 소수화 구조의 전환에 의한 영향이다. 다른 요인으로는 oxy-PAN 섬유와 용액간의 이온과 물의 교환, 이온의 농도차에 의한 삼투압 등이 영향을 준다. Oxy-PAN 섬유의 신장 및 수축과 기계적 특성에 영향을 미치는 여러 가지 요인들을 규명하기 위한 보다 많은 연구가 필요하지만, 본 연구실에서 제조된 oxy-PAN 섬유가 인공 근육 및 선형 구동체로 적용될 수 있는 충분한 가능성이 있음을 제시한다.

• 폴리머
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• 제25권4호
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• pp.602-607
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• 2001

이중 측쇄 이타코네이트 단위를 가지는 새로운 겔 전해질로 이용하기 위하여 bis(2-methoxyethyl)itaconate (bis(ME)I)를 itaconic acid와 2-methoxyethanol과 에스테르화 반응에 의하여 합성하였다. AN과 bis(ME)I의 공중합체들은 라디칼 중합에 의하여 AN/bis(ME)I = 9/1 ~ 1/1 조성을 가지는 것을 합성하였다. 최적의 기계적 성질과 이온전도도는 AN/bis(ME)I = 5/1 과 6/1 (25 ~ 35 wt%), LiClO$_4$(15 wt%) 그리고 가소제 (EC/PC=1/1) (40 ~ 50 wt%)에서 보여주었다. 가소화 겔 이온전도체는 질기고 안정된 기계적 성질을 보여주었으며 이온전도도는 8.12 ${\times}$ 10$_{-4}$ ~ 1.87 ${\times}$ 10$_{-3}$S/cm을 보여주었다. 최대 이온전도성을 보여주는 이온전도체는 전형적인 PEO를 중심으로 한 이온전도성 고분자보다 10배 이상 높은 이온전도성을 보여주었다.

• Bulletin of the Korean Chemical Society
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• 제30권10호
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• pp.2253-2258
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• 2009

wet spun polyacrylonitrile (PAN) fiber precursors. The process variables chosen were treatment temperature, applied tension in stabilization process. The temperature profile of the stabilization was set on the basis of exothermic peaks of the differential scanning calorimetry (DSC) result. Both tensile strength and modulus increased with holding at onset temperatures of the exothermic peaks for extended duration, and with a higher heating rate up to the onset temperatures at a given applied tension among the experimental conditions. The increase in load monotonously increased the tensile modulus, on the other hand, the tensile strength was maximum at the load of 15 mg/filament (T15). The load 20 mg/ filament (T20) was considered to be exceeded to form oriented crystalline structure, possibly introducing more defects in the fiber than under load of T15. The sample CP3-T15 O5 H30 showed the best tensile properties among the samples experimented whose tensile properties are compatible with the commercialized grade of general purpose carbon fibers even at low carbonization temperature such as $800\;{^{\circ}C}$ (the carbonization temperature in the commercial process. 1300∼$1500\;{^{\circ}C}$).

• 한국재료학회지
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• 제23권2호
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• pp.143-148
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• 2013

Well-distributed $SnO_2$-Sn-$Ag_3Sn$ nanoparticles embedded in carbon nanofibers were fabricated using a co-electrospinning method, which is set up with two coaxial capillaries. Their formation mechanisms were successfully demonstrated. The structural, morphological, and chemical compositional properties were investigated by field-emission scanning electron spectroscopy (FESEM), bright-field transmission electron microscopy (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). In particular, to obtain well-distributed $SnO_2$ and Sn and $Ag_3Sn$ nanoparticles in carbon nanofibers, the relative molar ratios of the Ag precursor to the Sn precursor including 7 wt% polyacrylonitrile (PAN) were controlled at 0.1, 0.2, and 0.3. The FESEM, bright-field TEM, XRD, and XPS results show that the nanoparticles consisting of $SnO_2$-Sn-$Ag_3Sn$ phases were in the range of ~4 nm-6 nm for sample A, ~5 nm-15 nm for sample B, ~9 nm-22 nm for sample C. In particular, for sample A, the nanoparticles were uniformly grown in the carbon nanofibers. Furthermore, when the amount of the Ag precursor and the Sn precursor was increased, the inorganic nanofibers consisting of the $SnO_2$-Sn-$Ag_3Sn$ nanoparticles were formed due to the decreased amount of the carbon nanofibers. Thus, well-distributed nanoparticles embedded in the carbon nanofibers were successfully synthesized at the optimum molar ratio (0.1) of the Ag precursor to the Sn precursor after calcination of $800^{\circ}C$.