• Journal of Microbiology and Biotechnology
• /
• v.23 no.9
• /
• pp.1308-1321
• /
• 2013

The emergence of microcarrier technology has brought a renewed interest in anchorage-dependent cell culture for high-yield processes. Well-known in vaccine production, microcarrier culture also has potential for application in other fields. In this work, two types of microcarriers were evaluated for small-scale monoclonal antibody (mAb) production by CHO-K1 cells. Cultures (5 ml) of microporous Cytodex 3 and macroporous CultiSpher-S carriers were performed in vented conical tubes and subsequently scaled-up (20 ml) to shake-flasks, testing combinations of different culture conditions (cell concentration, microcarrier concentration, rocking methodology, rocking speed, and initial culture volume). Culture performance was evaluated by considering the mAb production and cell growth at the phases of initial adhesion and proliferation. The best culture performances were obtained with Cytodex 3, regarding cell proliferation (average $1.85{\pm}0.11{\times}10^6$ cells/ml against $0.60{\pm}0.08{\times}10^6$ cells/ml for CultiSpher-S), mAb production ($2.04{\pm}0.41{\mu}g/ml$ against $0.99{\pm}0.35{\mu}g/ml$ for CultiSpher-S), and culture longevity (30 days against 10-15 days for CultiSpher-S), probably due to the collagen-coated dextran matrix that potentiates adhesion and prevents detachment. The culture conditions of greater influence were rocking mechanism (Cytodex 3, pulse followed by continuous) and initial cell concentration (CultiSpher-S, $4{\times}10^5$ cells/ml). Microcarriers proved to be a viable and favorable alternative to standard adherent and suspended cultures for mAb production by CHO-K1 cells, with simple operation, easy scale-up, and significantly higher levels of mAb production. However, variations of microcarrier culture performance in different vessels reiterate the need for optimization at each step of the scale-up process.

• Journal of the Korean Electrochemical Society
• /
• v.12 no.4
• /
• pp.324-328
• /
• 2009

The internal short-circuit between cathodes and anodes has been known to be a critical concern for the safety failures of lithium-ion batteries, which is strongly influenced by the thermal stability of separators. In this study, to effectively suppress the internal short-circuit failures, we developed a new composite separator with the improved thermal stability compared to conventional polyolefin-based separators. The composite separators were prepared by introducing a ceramic coating layer ($Al_2O_3$/PVdF-HFP) onto both sides of a polyethylene (PE) separator. The microporous structure of ceramic coating layers is determined by controlling the phase inversion of coating solutions and becomes more developed with the increase of nonsolvent (water) content. This structural change of ceramic coating layers was observed to greatly affect the thermal stability as well as the electrochemical performance of composite separators, which was systematically discussed in terms of phase inversion.

• Composites Research
• /
• v.35 no.6
• /
• pp.394-401
• /
• 2022

Two polymer precursors, polyvinylidene chloride-resin (PVDC-resin) and polyvinylidene fluoride (PVDF), are assembled into the microporous carbon by pyrolysis. Microporous carbon is advantageous as an electrode for supercapacitors that store electric charges through ion adsorption/desorption. The pyrolysis also turns the various heteroatoms of two precursors into functional groups, contributing to the additional charge storage. The analysis of the porous structure and function group during carbonization are important to develop the carbon for energy storage. Here, we analyzed the functional groups of two polymer-derived carbons through X-ray photoelectron spectroscopy. The electrochemical properties of the functional groups were explored in various pH electrolytes. The specific capacitance of two carbons in the acidic electrolyte (1 M H₂SO₄) was improved compared to that in the neutral electrolyte (0.5 M Na₂SO₄) due to the faradaic charge/discharge reaction of the quinone functional group. In particular, the carbon electrode derived from PVDC-resin exhibits a lower capacity than the carbon from PVDF due to the small micropores. In the alkaline electrolyte (6 M KOH), the highest specific capacitance and rate capability were obtained among the three electrolytes for both electrodes based on the facile adsorption of the constituent electrolyte ions (K⁺, OH^-).

• Proceedings of the Membrane Society of Korea Conference
• /
• 1996.04a
• /
• pp.16-19
• /
• 1996

Separation with synthetic membrane have become increasingly important processes in many fields. In the most application of membrane process, polymer membrane is used. the main advantage of polymers as a material for membrane preparation is the relative simplicity of this film formation which enables one to obtain rather high permeability rates. However, polymeric membranes have several limitations, such as high temperature instability, swelling and decomposition in organic solvent, et. al.. These limitations can be overcome by inorganic membrane. At the present time, commercially available inorganic membranes have pore diameters ranging 5nm to 50mm, and the predominant flow regime in such membrane is Knudsen diffusion. Since the Knudsen permeability is directly proportional to the molecular velocity, gases can be separated due to their molecular masses. However, this separation mechanism is only of important for light gases such as H2 and He. Other separation mechanisms like surface diffusion, active diffusion can play an important role only with very small pore diameters(2nm) and give rise to large permselectivities. Therefore, preparation of inorganic membrane with nano-sized pore have been attracting more and more attention.

• Carbon letters
• /
• v.12 no.3
• /
• pp.152-161
• /
• 2011

Activated carbon was prepared from pre-carbonized petroleum coke. Textural properties were determined from studies of the adsorption of nitrogen at 77 K and the surface chemistry was obtained using the Fourier-transform infrared spectrometer technique and the Boehm titration process. The adsorption of three aromatic compounds, namely phenol (P), p-nitrophenol (PNP) and benzoic acid (BA) onto APC in aqueous solution was studied in a batch system with respect to contact time, pH, initial concentration of solutes and temperature. Active carbon APC obtained was found to possess a high surface area and a predominantly microporous structure; it also had an acidic surface character. The experimental data fitted the pseudo-second-order kinetic model well; also, the intraparticle diffusion was the only controlling process in determining the adsorption of the three pollutants investigated. The adsorption data fit well with the Langmuir and Freundlich models. The uptake of the three pollutants was found to be strongly dependent on the pH value and the temperature of the solution. Most of the experiments were conducted at pH 7; the $pH_{(PZC)}$ of the active carbon under study was 5.0; the surface of the active carbon was negatively charged. The thermodynamic parameters evaluated for APC revealed that the adsorption of P was spontaneous and exothermic in nature, while PNP and BA showed no-spontaneity of the adsorption process and that process was endothermic in nature.

• Journal of the Korean Electrochemical Society
• /
• v.13 no.4
• /
• pp.240-245
• /
• 2010

This work explored the catalytic effect of Pt in multi-wall carbon nanotube and poly-pyrrole conductive polymer electrocatalysts (Pt/PPy/MWCNT). A home-made Pt/PPy/MWCNT catalyst was first evaluated by comparing its electrochemical active surface area (ESA) with E-Tek commercial catalysts by cyclic voltammetry in $H_2SO_4$ solution. Then, the methanol oxidation currents of Pt/PPy/MWCNT and the hydrogen peaks in $H_2SO_4$ solution were serially measured with microporous electrode. This provided the current density of methanol oxidation based on the ESA, allowing a quantitative comparison of catalytic activity. The current densities were also measured for Pt/C catalysts of E-Tek and Tanaka Precious Metal Co. The current densities for the different catalysts were similar, implying that catalytic activity depended directly on the ESA rather than charge transfer or electronic conductivity.

• Journal of Korea Foresty Energy
• /
• v.21 no.2
• /
• pp.17-24
• /
• 2002

Activated carbons were prepared from pine bark by steam activation, and pore structures and specific surface areas were then investigated. Three different types of kilns were used for the activation. When the stationary-vertical-or stationary-horizontal-type kiln was used for the steam activation to prepare an activated carbon from the bark, it was not possible to produce activated carbon having high specific surface areas exceeding 1,000 $m^2／g$. Using bark powder improved the specific surface area, but it was still not high enough. When the rotary-horizontal-type kiln was used for the activation, the activated carbons prepared had high specific surface areas of more than 1,000$m^2／g$, which was similar to a commercial first-grade activated carbon. The activated carbon prepared by the rotary kiln had a wide distribution of pore size ranging from microporous to mesoporous.

• Bulletin of the Korean Chemical Society
• /
• v.27 no.7
• /
• pp.981-985
• /
• 2006

Novel copolymers consisting of poly(2-hydroxyethyl aspartamide-co-N,N'-dimethyl-1,3-propane aspartamide) (PHEA-DPA) were prepared from polysuccinimide (PSI), which is the thermal polycondensation product of aspartic acid, via a ring-opening reaction with N,N'-dimethyl-1,3-propane diamine (DPA) and ethanolamine. The prepared water-soluble copolymer was then crosslinked by reacting it with hexamethylene diisocyanate to provide the corresponding gel. The swelling behavior and morphology of the crosslinked hydrogels were investigated. The degree of swelling decreased with increasing crosslinking reagent due to the higher crosslinking density. It was also confirmed that the swelling property is affected by pH. At low pH (< pH 4), swelling is increased due to the ionization of DPA with a tertiary amine moiety. In addition, a reversible swelling and de-swelling behavior was demonstrated by adjusting the pH of the solution. The prepared hydrogels showed a well-interconnected microporous structure with regular 5-20 $\mu$m sized pores.

• Polymer(Korea)
• /
• v.27 no.4
• /
• pp.307-312
• /
• 2003

Hollow fiber was prepared from the blend of a high density polyethylene (HDPE)/ultra high molecular weight polyethylene (UHMWPE). The changes in the morphology and mechanical property of the hollow fiber were investigated. The commercial product (Sterapore), having a high water permeability, was analyzed with viscosity measurement and FT-IR. The molecular weight of Sterapore was very high and its surface was coated with a vinyl alcohol/vinyl acetate copolymer. The content of UHMWPE in the HDPE/UHMWPE blend was limited below 10 wt%. In order to improve the dispersion of UHMWPE, a mineral oil should be introduced in the blend. The morphology and mechanical property of the hollow fiber of HDPE/UHMWPE blend were similar to those of the commercial product.

• Proceedings of the Materials Research Society of Korea Conference
• /
• 2009.11a
• /
• pp.46.1-46.1
• /
• 2009

산업이 점차 발달함에 따라 발생하는 환경오염으로 인해 인간의 삶에 있어 불가분의 관계에 있는 물에 대한 관심이 지속적으로 높아지고 있는 추세이다. 각종 질병의 요인이 되는 박테리아는 주로 물을 운송 매개체로 하기 때문에 이로 인한 물의 오염으로 인도의 경우 모든 질병 발생의 80%를 차지하는 것으로 세계보건기구(WHO)에 의해 보고되었다. 현재까지물 또는 공기의 항균 및 살균 정화를 위해 화학적, 생물학적 방식 등 다양한 기술이 개발되었으나 박테리아와같은 세균제거에는 무리가 있는 실정이다. 따라서 본 연구에서는 여러 물질 중에서도 특히 항균작용(Antibacterial activity)이 탁월한 은(Ag)을 나노입자화하여 in-situ 코팅을 통한 다공성 알루미늄 하이드록사이드 나노복합재의 제조함으로써 생물학, 생체의용공학, 약학 등에 응용될 수 있는 새로운 형태의 항균재료제조방법을 제안하였다. 우선, 다공성 알루미늄 하이드록사이드기판은 알루미늄 기판에 알칼리 표면개질을 실시함으로서 표면에 마이크로포어가 형성된 알루미늄 하이드록사이드 기판을 제조하였다. 이렇게 제조된 다공성 기판에 Polyol 공정으로 은나노입자를 합성 및 분산시킴으로서 in-situ로 은나노입자가 분산된 알루미늄 하이드록사이드 나노복합재 기판을 만들수 있었다. 본 연구를 통하여 제조된 은나노입자가 분산된 알루미늄 하이드록사이드 나노복합재 기판은 주사전자현미경(SEM) 및 투과전자현미경(TEM)을 통하여 미세구조와 상분석을 실시하였으며 X선 광전자분석(XPS)를 이용하여 기판 표면의 화학적 상태를 분석하였다.