• Membrane Journal
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• v.18 no.3
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• pp.219-225
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• 2008

In this research, polydimethylsiloxane-polymethylmethacrylate (PDMS-PMMA) block copolymer was synthesized from polydimethylsiloxane (PDMS) and methylmethacrylate (MMA) monomer using atom transfer radical polymerization (ATRP). The synthesis characterization of the PDMS-b-PMMA copolymer membrane was carried out by a FT-IR, $^1H$-NMR, GPC and DSC. The permeabilities of nitrogen and hydrogen gases were observed being $1.2{\sim}l.5$ barrer and $6.2{\sim}10.5$ barrer, respectively. Simultaneously, selectivities of hydrogen against nitrogen were $5.3{\sim}6.9$. The permeability and selectivity of PDMS-b-PMMA copolymer membrane were showed lower than the PDMS membrane, but higher than the PMMA membrane.

• Korean Journal of Optics and Photonics
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• v.8 no.1
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• pp.68-72
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• 1997

Using one of the absorption lines of $^{13}C_2H_2$ molecules near the zero dispersion wavelength(1549.49nm) of dispersion shifted fiber, we stabilized center frequency of an optical fiber Fabry-Perot filter. The free spectral range of the filter is 100 GHz for 100 GHz channel allocation. For equi-spaced three channel multiplexing, channel locking of three DFB-LDs to transmission peaks of the fiber Fabry-Perot filter was tried. To investigate the effect of dithering current applied to each DFB-LD, the change of DFB-LD linewidth was measured.

• Journal of the Society of Cosmetic Scientists of Korea
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• v.41 no.4
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• pp.315-324
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• 2015

In this study, we prepared liquid crystal emulsion composed of amphiphilic substance $C_{14-22}$ alcohol, $C_{12-20}$ alkyl glucoside, behenyl alcohol and studied liquid crystal emulsion of properties and in vitro skin permeation. The results of formulation experiments, the clear liquid crystalline structure was observed in the ratio of $C_{14-22}$ alcohol 0.8%, $C_{12-20}$ alkyl glucoside 3.2%, behenyl alcohol 4% in the formulation. The results of physical property measurements, the viscosity of liquid crystal emulsion and O/W emulsion applied as a control group was respectively $1871.26{\sim}1.15Pa{\cdot}s$, $1768.69{\sim}1.14Pa{\cdot}s$ and the shear stress of O/W emulsion was 178.68 ~ 909.18 Pa, that of liquid crystal emulsion was 190.45 ~ 919.38 Pa. The storage modulus of O/W emulsion was 3428.53 ~ 9157.45 Pa, that of liquid crystal emulsion was 4487.82 ~ 8195.59 Pa. The tan (delta) value of O/W emulsion which means a ratio of viscosity to elasticity was 0.43 ~ 0.19, and that of liquid crystal emulsion was 0.23 ~ 0.25. The water content value on the skin for liquid crystal emulsion was significantly higher from 1 h to 6 h compared with that of O/W emulsion and the transepidermal water loss on the skin was significantly superior in skin moisture loss suppression from 30 min to 4 h compared with that of O/W emulsion. The results of skin permeation using glycyrrhizic acid, the result of skin permeation amount of liquid crystal emulsion for 24 h was $64.58{\mu}g/cm^2$, that of O/W emulsion was $37.07{\mu}g/cm^2$, that of butylene glycol solution was $41.05{\mu}g/cm^2$. Hourly permeability results, it is showed that skin penetration effect of the liquid crystal emulsion increases after 8 h. These results suggest that liquid crystal emulsions are effective for skin moisturizing effect and function as potential efficacy ingredient delivery system for the transdermal delivery.

• Membrane Journal
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• v.25 no.4
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• pp.320-326
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• 2015

In this study, permeation experiments were carried out using the symmetric and asymmetric sinusoidal flux continuous operation (SFCO) modes for the submerged flat sheet membrane in the 0.5 wt% emulsion type cutting oil solution. The effective area and nominal pore size of the used microfiltration membrane were $0.02m^2$ and $0.15{\mu}m$, respectively. The emulsion cutting oil was rejected over 99% based on turbidity. Transmembrane pressure increased lower as the aeration rates increased. The symmetric SFCO mode was a little more effective than the symmetric SFCO mode in low permeate flux between 10 and $15L/m^2{\cdot}h$. However, the symmetric SFCO mode was shown very effectively in high permeate flux between 25 and $30L/m^2{\cdot}h$.

• Proceedings of the Korean Vacuum Society Conference
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• 2011.02a
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• pp.123-124
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• 2011

플라즈마 화학적 기상 증착(plasma enhanced chemical vapor deposition)공정 중 NH3 gas flow rate, RF power, SiH4 gas flow rate을 고정시키고 N2O gas flow rate을 0 sccm부터 250 sccm까지 변화시키는 조건 하에 SiON박막을 증착한 후 그 투과율, 굴절률을 측정하고 분석하였다. N2O gas flow rate조건별 시편들은 증착율을 계산하여 350 nm 두께로 동일하게 SiON을 증착하였고, borofloat위에 SiON을 증착한 샘플은 투과율을, 실리콘기판 위에 SiON을 증착한 샘플로는 굴절률을 측정하였다. 투과율의 경우는 UV/Vis spectrometer를 이용해 633 nm, 1550 nm 두 가지 파장 대 모두에서 N2O gas flow rate이 가장 큰 250 sccm일 때 가장 높은 것을 알 수 있었고 N2O gas flow rate이 낮아질수록 투과율 또한 작아지는 경향을 보였다. 굴절률은 ellipsometer를 이용해 측정하였으며 633 nm 파장에서 N2O gas flow rate가 가장 낮은 0 sccm일 때 굴절률이 가장 큰 값을 가지고 N2O gas flow rate이 커질수록 굴절률은 지수함수적으로 감소되었다(n=1.837~1.494). 이는 N2O gas flow rate이 낮을수록 SiN계열에 커질수록 SiO2계열에 가까워지는 현상으로 이해된다. 이러한 실험분석 결과는 향후 실리카 도파로의 설계 및 최적화를 위해 사용될 수 있다.

• Proceedings of the Membrane Society of Korea Conference
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• 1996.10a
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• pp.55-57
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• 1996

다공성 무기막은 높은투과도와 뛰어난 내열.내화학성, 그리고 경제성 때문에 기존의 PSA공정이나 증류와 같은 고에너지 분리공정을 대체하는 공정으로 각광을 받고 있다. 무기재료막의 제조하는 방법으로 주로 알콕사이드를 사용하는 솔-젤법(1)과 금속(2) 또는 기상반응(3)을 이용하는 화학증착법이 사용된다. 또한 고온에서 수소를 연속적으로 분리하여 화학평형에 기인한 한계를 극복하여 높은 수율을 얻고자하는 막반응기에 관한 연구가 활발히 진행되고 있다. 본 연구에서는 $\alpha$-알루미나 지지체의 미세한 다공성 구조 내부에서 TEOS(Tetraethylorthosilicate)와 산성의 알코올-물 혼합물을 확산시켜 실리카 솔을 생성시킴과 동시에 젤화시켜 기공의 크기를 감소시켜 막을 제조하였다. 이렇게 제조된 막은 높은 투과도와 낮은 수소선택도(selectivity=3-4)를 보였고, 두번째 단계로 silica sol을 제조하여 진공 하에서 dip-coating을 행하였다. 이렇게 2단계로 기공 구조를 개선시킨 실리카 막은 저압에서 상대적으로 높은 수소의 분리도(selectivity=5-7)를 보였으며 여전히 높은 투과도를 갖는다.

• Proceedings of the Korea Society for Energy Engineering kosee Conference
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• 1999.11a
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• pp.181-186
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• 1999

화학 축열 시스템의 성능을 모사하고 이를 해석하여 시스템 성능을 최적화하기 위해서는, 반응층의 열 및 물질 전달 특성을 정확히 아는 것이 중요하다. 본 연구에서는 $Na_2$S-$H_2O$ 반응계를 사용한 화학 열펌프에 대한 연구로, $Na_2$S-팽창흑연 복합체의 열전도도와 기체 투과도를 측정하였고, 소형 시스템을 제작하여 그 성능을 평가하였다. 열전도도는 전이 일차원 열류기법을 사용하여 측정하였고, 기체 투과도는 Darcy's law를 이용하여 측정하였다. 반응층의 열전도도와 기체 투과도는 팽창흑연 지지체의 겉보기 밀도와 반응염의 함량에 따라 각각 6~48W/mㆍK, 1.1$\times$$10^{-13}$~1.0$\times$$10^{-11}$m$^2$의 범위에 있었다. 또한 소형 시스템을 구성하여 445W/kgㆍ$Na_2$S의 냉방 출력을 얻을 수 있었다.

• Membrane Journal
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• v.25 no.2
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• pp.115-122
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• 2015

$SiO_2{\cdot}B_2O_3$ was prepared by trimethylborate (TMB)/tetraethylorthosilicate (TEOS) mole ratio 0.01 at $800^{\circ}C$. PDMS[poly(dimethysiloxane)]-$SiO_2{\cdot}B_2O_3$ composite membranes were prepared by adding porous $SiO_2{\cdot}B_2O_3$ to PDMS. To investigate the characteristics of PDMS-$SiO_2{\cdot}B_2O_3$ composite membrane, we observed PDMS-$SiO_2{\cdot}B_2O_3$ composite membrane using TG-DTA, FT-IR, BET, X-ray, and SEM. PDMS-$SiO_2{\cdot}B_2O_3$ composite membrane was studied on the permeabilities of $H_2$ and $N_2$ and the selectivity ($H_2/N_2$). Following the results of TG-DTA, BET, X-ray, FT-IR, $SiO_2{\cdot}B_2O_3$ was the amorphous porous $SiO_2{\cdot}B_2O_3$ with $247.6868m^2/g$ surface area and $37.7821{\AA}$ the mean of pore diameter. According to the TGA measurements, the thermal stability of PDMS-$SiO_2{\cdot}B_2O_3$ composite membrane was enhanced by inserting $SiO_2{\cdot}B_2O_3$. SEM observation showed that the size of dispersed $SiO_2{\cdot}B_2O_3$ in the PDMS-$SiO_2{\cdot}B_2O_3$ composite membrane was about $1{\mu}m$. The increasing of $SiO_2{\cdot}B_2O_3$ content in PDMS leaded the following results in the gas permeation experiment: the permeability of both $H_2$ and $N_2$ was increased, and the permeability of $H_2$ was higher than $N_2$, but the selectivity($H_2/N_2$) was decreased.

• Membrane Journal
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• v.23 no.2
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• pp.119-128
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• 2013

In this research, PEI/PEBAX composite hollow fiber membrane was used for the removal of water vapor from gases. PEI (Polyetherimide) substrate membrane was spinned by dry-wet phase inversion method and coated with PEBAX (Polyether block amides) 3533 and PEBAX1657. Fabricated fibers typically had an asymmetric structure of a dense top layer supported by a sponge-like substructure through scanning electron microscopy (SEM). $H_2O/N_2$ mixture gas was used to compare the performance of separation according to temperature, pressure and water activity. The results of PEBAX3533 and PEBAX1657 composite membranes respectively showed $H_2O/N_2$ selectivity of 61.7~118.5 and 85.3~175.4 according to operating conditions. PEBAX3533 composite hollow fiber membranes module showed the water vapor removal of 90%.

• Journal of the Society of Cosmetic Scientists of Korea
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• v.33 no.3
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• pp.189-196
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• 2007

In order to investigate the potential of very low molecular weight hyaluronic acid(oligo HA) as a cosmetic ingredient, we first measured its cytotoxicity in fibroblast, keratinocyte, and SIRC cell lines. For efficacy test, its moisturizing effect and penetration rate were evaluated in an artificial skin system and Caco-2 cells. Oligo HA did not show any cytotoxicity at a concentration of 300 ${\mu}g/mL$ in fibroblasts and 1,000 ${\mu}g/mL$ in keratinocytes but it showed weak proliferation. In vitro ocular test, oligo HA showed negligible cytotoxicity at the maximum concentrations used(2,000 ${\mu}g/mL$) in SIRC cells. In the test of the single and repeated cutaneous applications, oligo HA under occlusive patch did not provoke any cumulative irritation and sensitization. Oligo HA at a concentration of 0.01 % exhibited a more potent moisturizing effect than hyaluronic acid at a concentration of 0.01 %. In the permeability test using artificial skin and Caco-2 cell lines, hyaluronic acid(M.W. $1.1{\times}10^6$) was hardly observed in the down medium of the inserts. On the other hand, oligo HA(M.W. 5,000) was detected in the down medium up to 16.0 % at 6 h in Caco-2 cell culture and up to 90 % at 6 h in an artificial skin system. These results suggest that oligo HA could be useful as an active ingredient for cosmetics.