• 한국대기환경학회지
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• 제15권4호
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• pp.417-428
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• 1999

The measurement of VOSCs(volatile organic sulfur compounds) in the air is nowadays a very important environmental research field. It is, however, very difficult because the concentration of the VOSC in ambient air is usually very low and the high reactivity makes it difficult to keep in container without loss of recovery. In this study, sampling method with cryogenic preconcentration is evaluated for analysis of atmospheric VOSC such as $CH_3SH,\;CH_3CH_2SH,\;CH_3SCH_3,\;CS_2,\;CH_3SSCH_3,\;CH_3SCH_2SCHA_3,\;and\;C_2H_5SSC_2H_5$ analyzed by GC-MS or GC-FID. Repeatabilities of measurement accompanied with preconcentration for 3-successive runs were in the range of 0.2~1.0% as a relative standard deviation. Stabilities up to 13 days were measured in 6 L canister and 10 L tedlar bag filled with VOSCs in ppb level. Higher stability was observed in tedlar bag as compared to canister with glass coated inner walls, and thiol compounds show dramatic losses in canister within 2~3 days. It is found that recovery over 70% was obtained in a week for all tested VOSCs when the compounds from ambient air matrix were stored in tedlar bag. It is also found that the stabilities of VOSCs are depending on humidity and coexisting compounds in matrix gas due to sample adsorption onto inner surface and reactivity. The results indicate the possibility and limitations of VOSC analysis in ambient air using container sampling method with cryogenic preconcentration.

• 한국응용과학기술학회지
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• 제28권3호
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• pp.321-328
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• 2011

The autothermal reforming reaction of methane was investigated to produce hyd rogen with Ni/$CeO_2-ZrO_2$, Ni/$Al_2O_3$-MgO and Ni-Ru/$Al_2O_3$-MgO catalysts. Honeycomb metalli c monolith was applied in order to obtain high catalytic activity and stability in autothermal r eforming. The catalysts were characterized by XRD, BET and SEM. The influence of various catalysts on hydrogen production was studied for the feed ratio($O_2/CH_4$, $H_2O/CH_4$). The $O_2/CH_4$ and $H_2O/CH_4$ ratio governed the methane conversion and temperature profile of reactor. Th e reactor temperature increased as the reaction shifted from endothermic to exothermic reactio n with increasing $O_2/CH_4$ ratio. Among the catalysts used in the experiment, the Ni-Ru/$Al_2O_3$-MgO catalyst showed the highest activity. The 60% of $CH_4$ conversion was obtained, and th e reactor temperature was maintained $600^{\circ}C$ at the condition of GHSV=$10000h^{-1}$ and feed ratio S/C/O=0.5/1/0.5.

• 멤브레인
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• 제24권3호
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• pp.185-193
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• 2014

고무상 고분자인 PDMS (polydimethylsiloxane)에 HNT (halloysite nanotube)의 함량을 5, 10, 20, 30 wt%로 달리하여 PDMS-HNT 복합막을 제조하고, FT-IR, XRD, TGA, SEM에 의해서 막의 특성을 조사하였다. 기체투과 실험은 $25^{\circ}C$, $3kg/cm^2$ 조건에서 수행하였고, PDMS-HNT 복합막의 HNT 함량 변화에 따른 $H_2$, $N_2$, $CH_4$, $CO_2$들의 기체투과도와 선택도를 조사하였다. $H_2$, $N_2$, $CH_4$, $CO_2$의 투과기체에 대해 HNT 함량이 0~30 wt% 범위에서 HNT 함량이 증가할수록 기체들의 투과도는 전체적으로 감소하는 경향을 보였다. 선택도($CO_2/N_2$)는 14~44의 값을 보였고, 선택도($CO_2/CH_4$)는 3.0~7.7의 값을 보였다.

• 멤브레인
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• 제18권3호
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• pp.226-233
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• 2008

PTMSP에 $0{\sim}20$ wt% PMMH dendrimer 나노입자를 가하여 PTMSP/PMMH dendrimer 복합막을 제조하였다. 복합막의 기체 투과특성에 미치는 PMMH denimer의 영향을 조사하였다. $H_2,\;N_2,\;CO_2,\;CH_4$의 투과도는 PTMSP 내 PMMH endrimer의 함량이 증가하면서 감소하였다. PTMSP/PMMH dendrimer 복합막에서 수소를 제외한 다른 기체들의 투과도 순서는 $N_2\;<\;CH_4\;<\;CO_2$이며, 이것은 기체의 임계온도의 순서 $N_2\;<\;CH_4 <\;CO_2$와 일치하고 있다. $N_2$에 대한 기체의 선택도는 PTMSP 내의 PMMH denimer의 함량이 증가하면서 증가하였다. $CO_2/N_2$ 선택도는 5.6에서 16.9로 증가하였다.

• 폴리머
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• 제27권6호
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• pp.528-535
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• 2003

불소계 섬유용 발수$.$발유제의 제조에 일반적으로 쓰이는 과불소알킬아크릴레이트 및 노말알킬아크릴레이트의 공중합체를 유화 중합법으로 제조할 시 계면활성제, 유기용매, 내구성 향상 목적으로 소량 첨가되는 기능성 단량체 및 공중합체의 결정 용융 온도 (T$_{m}$ )변화에 따른 고분자 라텍스의 입자 직경 변화와 그들의 표면 특성 (접촉각 및 발수도)의 변화를 관찰하였다 또한 WAXD 실험을 통해 공중합체의 T$_{m}$ 의 변화에 따른 공중합체의 곁사슬의 채움구조 변화를 조사하였으며 이를 통해 표면 특성과의 관계를 연구하였다. 그리고 과불소알킬아크릴레이트와 더불어 말단기가 약간 다른 불소아크릴레이트, [CH$_2$= CH$CO_2$CH$_2$(CF$_2$CF$_2$)nH] (n=4,5,6)를 사용한 불소아크릴레이트 공중합체도 동시에 합성하여 공중합체의 곁사슬의 채움구조, 말단기($CH_3$-,CF$_3$-,CHIF$_2$-)의 종류 및 농도변화에 따른 표면 특성 (접촉각, 발수도 등)의 변화를 관찰하였다.

• 한국전기전자재료학회논문지
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• 제22권5호
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• pp.448-454
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• 2009

Hydrogen was produced from water plasma excited in high frequency (HF) inductively coupled tubular reactor. Mass spectrometry was used to monitor gas phase species at various process conditions, Water dissociation rate depend on the process parameters such as ICP power, $H_{2}O$ flow-rate and process pressure, Water dissociation percent in ICP reactor decrease with increase of chamber pressure, while increase with increase of ICP power and $H_{2}O$ flow rate. The effect of $CH_4$ gas addition to a water plasma on the hydrogen production has been studied in a HF ICP tubular reactor. The main roles of $CH_4$ additive gas in $H_{2}O$ plasma are to react with 0 radical for forming $CO_x$ and CHO and resulting additional $H_2$ production. Furthermore, $CH_4$ additives in $H_{2}O$ plasma is to suppress reverse-reaction by scavenging 0 radical. But, process optimization is needed because $CH_4$ addition has some negative effects such as cost increase and $CO_x$ emission.

• Korean Chemical Engineering Research
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• 제45권6호
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• pp.663-668
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• 2007

$Ni/CeO_2-ZrO_2$ 촉매를 이용하여 수소 제조를 위한 메탄의 자열개질반응 특성을 조사하였다. 메탄의 자열개질반응에서 촉매의 활성과 안정성을 향상시키기 위해 알루미나가 코팅된 금속 모노리스를 사용하였으며, 금속모노리스 촉매체는 높은 반응온도에서 분말형태의 촉매에 비해 높은 메탄 전환율을 나타내었다. 자열개질반응에 있어서 $H_2O/CH_4/O_2$의 비는 전환율에 영향을 미치는 중요한 변수임을 알 수 있었다. $H_2O/CH_4$ 비가 증가함에 따라 수소 수율은 증가되고, 또한 $O_2/CH_4$ 비가 증가함에 따라 메탄 전환율은 증가하지만 수소 수율은 감소하였다. $Ni/CeO_2-ZrO_2$ 촉매에 0.5 wt%의 귀금속 촉매인 Ru 첨가로 인해 낮은 반응온도에서 촉매 활성이 향상되었다.

• 분석과학
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• 제21권5호
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• pp.432-437
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• 2008

본 연구에서 초음파 조사하에서 Mg 전극을 사용하여 $CH_3HSiCl_2$, $PhSiCl_3$, $CH_3SiCl_3$ 및 $(CH_3)_2SiCl_2$와 같은 여러 가지 모노머를 가지고 전기환원법에 의하여 폴리실란을 합성하였다. 또한 반응속도에 있어서 모노머와 첨가제 (p-dibromobenzene (DBB), naphthalene (NAPH) 및 anthracene (ANTH))의 효과를 연구하였다. 네 종류의 모노머중에서 $PhSiCl_3$의 고분자화 반응은 아주 높은 반응속도를 보였다. 또한, p-dibromobenzene(DBB)는 가장 좋은 첨가제로 입증되었다. 이들 관찰에 근거하여 이들의 고분자화 반응에서 가능한 반응 메커니즘을 제시하였다.

• 대한화학회지
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• 제42권6호
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• pp.679-695
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• 1998

A series of ${\alpha}{\omega}-bis[4-(4'-(S)-(+)-2-methylbutylbiphenyl-4-carboxy)phenoxy]alkanes$, were synthesized, and their thermal and liquid crystalline properties were studied. The chain length of the central polymethylene spacers, x, of the chiral twin compounds was varied from 3 to 12. These compounds were characterized by elemental analysis, IR and NMR spectroscopy, differential thermal analysis (DSC), and crosspolarized microscopy. All compounds were found to be enantiotropic liquid crystalline, and the values of melting $(T_m)$ and isotropization temperature $(T_i)$ as well as ${\delta}H_I$ and ${\delta}S_I$ decreased in a zig-zag fashion, revealing the so called odd-even effect as x increased. Their mesomorphic properties fell into four categories depending upon x; (a) compounds with x=3, 4 and 5 formed only a cholesteric phase on heating, while on cooling they went through two transitions of isotropic (I)-to-cholesteric (Ch) and Ch-to-smectic $A\;(S_A)$ phases before crystallization. (b) compounds with x=6, 8 and 10 exhibited only a cholesteric phase both on heating and on cooling. (c) compounds with x=7 and 9 went through three transitions of crystal $(C)-to-S_A,\;S_A-to-Ch,$ and Ch-to-I phases on heating while on cooling they went through four transitions of I-to-Ch, $Ch-to-S_A,\;S_A-to-Smectic\;C\;(S_C),\;and\;S_c-to-C$ phases in that order, and (d) compounds with x=11 and 12 went reversibly through four transitions of $C-to-S_C,\;S_C-to-S_A,\;S_A-to-Ch,$ and Ch-to-I phases.

• Macromolecular Research
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• 제16권5호
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• pp.441-445
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• 2008

A series of aluminum complexes supported by $\beta$-ketoamino, ligand-bearing, 3-position substituents $LAlEt_2$ ($L=CH_3C(O)C(Cl)=C(CH_3)NAr\;(L_1)$, $L=CH_3C(O)C(H)=C(CH_3)NAr\;(L_2)$, $L=CH_3C(O)C(Ph)=C(CH_3)NAr\;(L_3)$, and $L=CH_3C(O)C(Me)=C(CH_3)NAr\;(L_4)$, $Ar=2,6-^iPr_2C6H_3$) were synthesized in situ and employed in the ring-opening polymerization (ROP) of $\varepsilon$-caprolactone ($\varepsilon$-CL) and cyclohexene oxide (CHO). The 3-position substituents on the $\beta$-ketoamino ligand backbone of the aluminum complexes influenced the catalyst activity remarkably for both ROP of $\varepsilon$-CL and CHO. Aluminum $\beta$-ketoamino complexes displayed different catalytic behavior in ROP of $\varepsilon$-CL and CHO. The order of the catalytic activity of $LAlEt_2$ was $L_1AlEt_2$>$L_2AlEt_2$>$L_3AlEt_2$>$L_4AlEt_2$ for ROP of $\varepsilon$-CL, being opposite to the electron-donating ability of the 3-position substituents on the $\beta$-ketoamino ligand, while the order of the catalytic activity for ROP of CHO was $L_1AlEt_2$>$L_3AlEt_2$>$L_4AlEt_2$>$L_2AlEt_2$. The effects of reaction temperature and time on the ROP were also investigated for both $\varepsilon$-CL and CHO.