• 공업화학
• /
• 제28권1호
• /
• pp.57-63
• /
• 2017

본 연구에서는 다양한 NCO index에서 물 함량 변화가 자동차용 폴리우레탄 시트 폼 패드의 정적 안락감에 미치는 영향을 알아보았다. 정적 안락감에 영향을 미치는 요인을 파악하기 위해 UTM을 사용한 정하중 특성 시험을 통하여 히스테리시스 곡선을 나타냈으며, 이를 통해 25% 변형 시 경도와 65% 변형 시 경도, hysteresis loop area, hysteresis loss (%), 그리고 Sag factor를 구하였다. 동일한 NCO index에서 물 함량이 증가함에 따라 우레아 결합의 증가로 경도가 증가하고, 가교밀도가 증가하는 경향을 swelling ratio 측정으로 확인하였으며, 이에 따라 복원력은 감소하는 경향을 확인하였다. 또한 표면 경도의 증가로 인해 Sag factor가 감소하는 경향을 확인하였다. 동일한 물 함량에서 NCO index가 증가함에 따라 우레탄과 우레아 결합이 이소시아네이트와 추가 반응하여 가교도와 경도가 증가하고 이에 따라 복원력이 감소함을 확인하였다.

• 한국세라믹학회지
• /
• 제13권1호
• /
• pp.11-19
• /
• 1976

Carbon bond 흑연도가니는 clay bond 형 흑연도가니에 비하여 열전도율이 크고 열팽창율이 적으며, 열간하중성이 좋을 뿐 아니라 열충격에도 안전하여 그 사용 수명이 100여회나 된다. 본 연구결과 carbon bond 형 흑연도가니의 제조에 적합한 원료의 조합비는 인장흑연 40, 탄화규소 15, Ferro-silion 25, 무기질결합제 15, 영정석 3, ferromanganese 2 였으며, 흑연도가니 제조에 소요되는 원료들의 상호관계는 흑연량이 증가할수록 산화율 및 기공률이 증가하고, 기공률의 증가도 흑연의 산화량에 비례하였으며, 탄화규소의 증가는 산화율 및 기공률을 증가 시켰고 ferrosilion의 증가는 기공률 및 산화율에 별영향을 미치지 않었고, 유리질의 증가는 산화율 및 기공율을 감소시키나 과량이면 bloating현상이 일어나 오히려 기공률이 커졌다. 제조된 도가니의 물성은 부피비중2.31, 겉보기비중 2.58, 기공률 15.2%, 흡수율 6.01%, 압축강도 438kg/$cm^3$, 인장강도 256kg/$cm^3$, 산화소모율 3.77%이하이며 평균사용 수명은 105회였다.

• Bulletin of the Korean Chemical Society
• /
• 제34권12호
• /
• pp.3641-3648
• /
• 2013

Energy transfer and bond dissociation of $C-H_{methyl}$ and $C-H_{ring}$ in excited toluene in the collision with $H_2$ and $D_2$ have been studied by use of classical trajectory procedures at 300 K. Energy lost by the vibrationally excited toluene to the ground-state $H_2/D_2$ is not large, but the amount increases with increasing vibrational excitation from 5000 and $40,000cm^{-1}$. The principal energy transfer pathway is vibration to translation (V-T) in both systems. The vibration to vibration (V-V) step is important in toluene + $D_2$, but plays a minor role in toluene + $H_2$. When the incident molecule is also vibrationally excited, toluene loses energy to $D_2$, whereas it gains energy from $H_2$ instead. The overall extent of energy loss is greater in toluene + $D_2$ than that in toluene + $H_2$. The different efficiency of the energy transfer pathways in two collisions is mainly due to the near-resonant condition between $D_2$ and C-H vibrations. Collision-induced dissociation of $C-H_{methyl}$ and $C-H_{ring}$ bonds occurs when highly excited toluene ($55,000-70,400cm^{-1}$) interacts with the ground-state $H_2/D_2$. Dissociation probabilities are low ($10^{-5}{\sim}10^{-2}$) but increase exponentially with rising vibrational excitation. Intramolecular energy flow between the excited C-H bonds occurring on a subpicosecond timescale is responsible for the bond dissociation.

• Bulletin of the Korean Chemical Society
• /
• 제18권8호
• /
• pp.874-880
• /
• 1997

Various classes of phospholipids were investigated for the structural determination of fatty acyl groups by fast atom bombardment tandem mass spectrometry (FAB-MS/MS). Phospholipids were desorbed by FAB as molecules chelated with sodium ion (or ions). Collision-induced dissociation (CID) of intact sodium adduct molecular ions ([M+Na]+, [M-H+2Na]+ or [M+Na-2H]-) produced a series of homologous fragment ions via the charge-remote fragmentation along the fatty acid chains. These ions were found useful to locate the double bond positions even for the polyunsaturated fatty acid chains. The regiospecificity of the acyl chain linkages in phosphatidylcholine (PC) could also be determined based on the ratio of relative abundance of the product ions (i.e., [M+Na-85-R2COOH]+ vs [M+Na-85-R1COOH]+) in CID-MS/MS of [M+Na]+. These are generated by the loss of fatty acyl groups at sn-1 and sn-2, respectively, together with the choline group. In all the phospholipid compounds investigated, loss of the fatty acid at the sn-2 position was dominant. The present method was applied to the structural determination of molecular species of phosphatidylglycerols (PG) isolated from cyanobacterium Synechocystis sp. PCC 6803.

• Bulletin of the Korean Chemical Society
• /
• 제18권1호
• /
• pp.66-70
• /
• 1997

The polymerization of 4, 4-bis(acetoxymethyl)-1, 6-heptadiyne (BAH) was carried out by MoCl5 and WCl6 with various organometallic cocatalysts. MoCl5-based catalysts were more effective than WCl6-based ones for the cyclopolymerization of BAH. Poly(BAH) was characterized to have polymer backbone with conjugated double bond and cyclic structure by IR, UV-visible, and 1H-and 13C NMR spectroscopies. The polymer was stable up to 310 ℃ and 5 % weight loss show up at 350 ℃. The resulting dark violet polymer exhibited good solubility in common organic solvents and could be cast on a glass plate to give film with good mechanical properties. It was found that oxygen permeability (PO2) and permselectivity (PO2/PN2) of the resulting polymer were 15.2 barrer and 2.84, respectively.

• Bulletin of the Korean Chemical Society
• /
• 제13권1호
• /
• pp.83-87
• /
• 1992

The ring expansion of 1,3-thiazolidines 4 derived from ${\beta}$-ketoacid derivatives to the corresponding dihydro-1,4-thiazines 1 by using the action of chlorine on 4 has been achieved. In the chlorinolysis unisolable sulfenyl chlorides 5 may be formed from chlorosulfonium ions 11 by ${\beta}$-elimination involving carbonyl activated methylene hydrogens. Addition of sulfenyl chloride to the internal double bond appears to form probable thiiranium ions 14, which in turn gave 1 with loss of acidic proton. Imminium ions 15 could be hydrolyzed easily to give enol 8. As a side reaction, dihydrothiazine that was formed was further chlorinated to produce dichlorides 16 which were rearranged readily to the chloromethyl compounds 10.

• Bulletin of the Korean Chemical Society
• /
• 제21권4호
• /
• pp.412-418
• /
• 2000

Association of cytochrome c with anionic membranes involved both electrostatic and hydrophobic interactions and their relative contributions depended on the physical state of the membrane and the redox state of cyto-chromec.Hydrophobic interaction was favored by the membranes in gel phase, by the membranes with a large curvature, and by the membranes with a high surface charge density. Ferrocytochrome c was less dissociable by NaCl than ferricytochrome c suggesting that a lower protein stability is beneficial for hydrophobic interac-tion.Hydrophobic interaction induced larger structural perturbations on cytochrome c as monitored by the loss of the Fe-Met bond and by the increase in the distance between heme and Trp-59. When bound to anionic mem-branes,spin-labeled cytochrome c showed an electron paramagnetic resonance spectrum with two or more components, providing a direct evidence for multiple conformations of bound cytochrome c.

• Bulletin of the Korean Chemical Society
• /
• 제21권6호
• /
• pp.557-561
• /
• 2000

Various enaryloxynitriles-terminated reactive polymer precursors containing rigid aromatic units were prepared from various diamines and 1-(p-formylphenyl)-1-phenyl-2,2-dicyanoethene (1). Arylate end-capped model compounds linked with azomethine bond were also prepared by reacting p-formylphenyl benzoate with diamines to compare the curing ability. The oligomers were highly soluble in polar aprotic solvents such as N,N-dimethylformamide, dimethylsulfoxide and N-methyl-2 -pyrrolidinone. They generally showed an exothermic curing process between $280-350^{\circ}C$, attributable to the thermal crosslinking of the dicyanovinyl group in DSC analysis, and no weight loss at curing temperature. Upon heating the polymer precursors, heat-resistant and insoluble network polymers were obtained. Thermogravimetric analyses of the precursors containing rigid aromatic units showed thermal stability with a 77-92% residual weight at $500^{\circ}C$ under nitrogen.

• Bulletin of the Korean Chemical Society
• /
• 제7권4호
• /
• pp.311-314
• /
• 1986

A series of tetramethyl 1-substituted benzyl-3a,7a-dihydro-1H-indole-2,3,3a,4-tetracarboxylates were prepared and their reactions with bromine were examined. The initial reaction seemed to be the formation of the intermediate N-bromo quaternary ammonium bromide. This intermediate underwent aromatization with loss of the 3a-methoxycarbonyl group. Bromine replaced the N-substituent of the p-methoxybenzyl compound and addition of bromine occurred across the $C_6-C_7$ double bond of the indole ring. Bromination of the benzyl ring and aromatization occurred for the m-methoxybenzyl compound.

• 한국펄프종이공학회:학술대회논문집
• /
• 한국펄프종이공학회 2006년도 PAN PACIFIC CONFERENCE vol.1
• /
• pp.129-136
• /
• 2006

Although cleaner and cheaper deinking of ONP could be performed at the neutral or low alkaline condition excessive loss from froth-flotation is unavoidable and so reduction of alkali or caustic soda dosage sacrifices recycling yield. Now the new trade-off regarding alkali dosage versus flotation yield is urgently required in order to set the optimized neutral or low alkaline deinking process of ONP. Lipase from Thermomyces Lanuginosus has an effect on desizing and deacetylation reaction and it could be applied to the stock of pre flotation secondary stage in order to reduce the flotation reject without the sacrifice of optical properties of flotation accepts. Instead of inorganic base, lipase could be applied as a biochemical catalyst for the selective modification of valuable hydrophobic particles in deinking stock, for example cellulose fines and inorganic fillers covered by hydrophobic additives or contaminants. When the enzymatic hydrolysis of ester bond could be made on the surface of hydrophobic particulates, unwanted float of fine particles could be prevented. Now the enhancement of flotation selectivity or the modification of the hydrophobicity of deinking stock is expected to be promoted by the enzymatic pre treatment. And the reduction of recycling cost with the saves of raw material, recovered paper would be possible as a result.