• Applied Chemistry for Engineering
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• v.4 no.3
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• pp.627-636
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• 1993

Anionic acrylic resin utilizing macromer(TBMA-g-MMA) copolymer was synthesized by preparing (TBMA) macromer using anionic living polymerization, followed by graft copolymerization with MMA macromer. To control the anionic site content in graft copolymer, the relative composition((TBMA) macromer/MMA ratio) of the graft copolymer was controlled at 7/3, 10/90, 15/85, 20/80, 30/70, 40/60, 50/50 in weight content. In the course of anionic living polymerization of(TBMA) macromer, broad molecular weight distribution (1.4~1.5) was obtained by using n-butyllithium-diphenyethylene initiatior system at $-78^{\circ}C$. To introduce the double bond at the end of chain in termination step, methacryloyl chloride was reacted after insertion of benzaldehyde as capping material. Moreover, TBMA parts in graft copolymer were hydrolyzed in the presence of p-toluenesulfonic acid catalyst, and neutralization of graft copolymer with triethylamine was granted acrylic resin to anionic site. Molecular weight and molecular weight distribution of(TBMA) macromer were determined by GPC, and the hydrolysis of TBMA with neutralization of acrylic resin were determined by IR and NMR. From water dispersion and stability point of view, stable dispersion state appeared at low molecular weight(TBMA) macromer with a small TBMA content as a result of scrutiny about the relation to TBMA content and branch length for(TBMA) macromer molecular weight in graft copolymer.

• Journal of the Korean Society of Food Science and Nutrition
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• v.29 no.4
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• pp.635-641
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• 2000

In order to utilize the protein source from a fish proessing by-product, cod was hydrolyzed with various enzymes such as tuna pyloric caeca crude enzyme (TPCCE), a-chymotrypsin, trypsin, papain and pronase E. The TPCCE hydrolysate acquired the highest sensory properties on taste, odor and color. The resultant cod rfame protein hydrolysate (CFPH) which was hydrolyzed with TPCCE, was separated through a series of ultrafiltration membranes with molecular weight cut-off (MWCO) of 30, 10, 5 and 1 kDa, and four types of permeates in cluding 30 K (permeate from 30 kDa membrane), 10 K (permeate from 10 kDa membrane), 5 K (permeate from 5 kDa membrane) and 1 K (permeate from 1 kDa membrane) were obtained. The natural sauces were prepared with 30 K, 10 K, 5 K and 1 K hydrolysate, and the sauce prepared with 1 K hydrolysate was the best score in sensory evaluations. In addition the mixed sauce prepared with 1 K hydrolysate and commercial soy sauce was similar to commercial sauce in sensory properties. These results suggest that the mixed sauce would be utilized as the substitute of acid-hydrolysis sauce.

• Applied Chemistry for Engineering
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• v.9 no.4
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• pp.561-564
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• 1998

The radial distribution functions of a linear spheroidal type gas molecule $C_2H_4$ were calculated by using the Stockmayer molecular molel, which assumed the $C_2H_4$ molecule as simple quadrupolar molecule. To examine the validity of the calculated radial distribution of $C_2H_4$ gas, the density dependent pressures of $C_2H_4$ gas at several temperatures were calculated and compared with literarily known experimental pressure data of $C_2H_4$ gas. The temperatures examined was 50, 100 and $150^{\circ}C$ and the densities were up to $0.02/{\AA}^3$ (maximum pressure = 1500 atm). The radial distribution function expression used was derived by Yoon, Hacura, and Baglin (YHB) with Baker and Henderson's perturbation theory. The calculated results by a computer showed that the $C_2H_4$ pressures calculated agreed well with the experimental values within ${\pm}5%$ of error range. This indicated that the YHB radial distribution function expression is good enough to obtain various physical quantities sensitive to density such as pressure with resonable accuracy.

• Korean Journal of Food Science and Technology
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• v.23 no.3
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• pp.366-369
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• 1991

In order to elucidate texturization mechanism of extrudated protein, egg white lysozyme was heated under high pressure conditions, and its solubility and changes of molecular weight were investigated. Under high pressure conditions of $100,\;300\;and\;600\;kg/cm^2$, solubility decreased gradually with increasing temperature in the samples heated at $70,\;120\;and\;150^{\circ}C$ and decreased notably with increasing pressure at $200^{\circ}C$. Polymerization was found in the samples heated at $150\;and\;200^{\circ}C$ while a band which located below monomer(low-molecular) could be recognized. Molecular weight of the low-molecular was estimated to be about $6,000{\sim}9,000$ and no smaller peptide was recognized. The polymerization may have occured by disulfide crosslinking in the samples heated at $120^{\circ}C$ but other crosslinking may have played a role in those at $150\;and\;200^{\circ}C$.

• The Korean Journal of Rheology
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• v.8 no.2
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• pp.103-118
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• 1996

변형된 Maxwell 모델을 모의 데이터와 폴리스티렌의 동적 실험 데이터인 G＇과 G ＂에 적용하여 연속 완화시간 스펙트럼을 결정하였고, Maxwell 모델을 사용했을 때 얻어지 는 불연속 완화시간 스펙트럼과 비교하였다. MGMM과 GMM 모두 선형회귀 방법과 비선 형회귀 방법을 사용하여 완화시간 스펙트럼을 결정하였는데 비선형 방법을 사용했을 때 선 형방법에 비해 좀 더 만족스러운 결과를 얻을수 있었다. 모의 데이터의 경우 사용한 완화시 간의 수가 많은 경우에는 MGMM과 GMM 모두 원래의 스펙트럼을 잘 재현했으나 완화시 간의 수가 작은 경우에는 MGMM이 GMM에 비해 원래의 완화시간 스펙트럼을 보다 잘 나 타내었다. 또 단분산성폴리스티렌의 경우 MGMM과 GMM의 완화시간 스펙트럼이 모두 작 은 완화시간 영역에서는 분자량에 무관했고 큰 완화시간 영역에서는 분자량이 커질수록 스 펙트럼이 완화시간이 커지는 쪽으로 이동하였다. 또 두드러진 terminal 완화시간을 볼수 있 었다. 그러나 다분산성 폴리스티렌의 경우에는 단분산성의 경우와는 달리 두드러진 terminal 완화시간을 볼수 없었다. 그리고 MGMM의 파라미터 m은 분자량 분포에 크게 의존함을 알 수 있었으며 연속 완화시간 스펙트럼에서 계산된 불연속 완화시간 스펙트럼이 GMM에서 얻어진 불연속 완화시간 스펙트럼과 잘 일치함을 볼수 있었다.

• The tire
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• s.75
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• pp.15-23
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• 1978

금속염을 첨가한 고무를 아연판과 접착가황하여 아연면의 첨가금속과 유황의 분포를 XMA에 의해 구했다. 가황중에 아연면으로 이행하는 것은 Co, Cu, Pb를 포함한 유기금속염뿐이였다. 고무 속의 유리유황도 이들 금속염과 함께 아연판으로 이행되어 왔다. 나프텐산코발트 중의 Co는 아연층내에 확산되어 분포된 데 반하여, S는 아연판표면에만 분포되어 있다. 양자가 아연판으로 이행되는 양은 첨가량에 비례해서 증가하였다. 고무와 아연판의 접착력은 Co량 0.6%까지는 증가하고, 그 이상의 첨가에서는 현저하게 저하되었다. 나프텐산코발트의 첨가량을 증가시키면 가황고무 중의 망목쇄농도는 변하지 않으나 유리유황은 감소하였다. 가황고무 중의 잔류나프텐산코발트는 60℃이상의 열처리온도에서 산화를 촉진하고 접착력도 저하시킨다. 카아본블랙을 배합하지 않은 NR의 유전거동보다 첨가한 나프텐산코발트는 가황온도에서 고무 분자의 주쇄 Segment의 완화 mode에 영향을 준다는 것을 알았다.

• Proceedings of the Korean Environmental Sciences Society Conference
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• 2016.10a
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• pp.96-96
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• 2016

• Polymer(Korea)
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• v.36 no.6
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• pp.693-698
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• 2012

In this study aluminum isopropyl oxide ($Al(O-i-Pr)_3$) was supported on the amine-functionalized surface of silica to synthesize high molecular weight (MW) polylactide (PLA), and it was tested for PLA polymerization behaviors. A silica was funtionalized with silane compound having amine groups, then in-situ treated with $Al(O-i-Pr)_3$. $Al(O-i-Pr)_3$ attached to amine group on silica showed activity only in the presence of MAO (methyl aluminoxane). At the polymerization temperature of $115^{\circ}C$, the conversion and the MW of PLA were increased as the amount of silane was increased. At the polymerization temperature of $130^{\circ}C$, the conversion was decreased while the MW was increased drastically and reached to MW 44000 g/mol when the amine concentration was 3.0 mmol/g. A bimodal type GPC curve was shown at the polymerization temperature of $115^{\circ}C$. As the amount of amine group increased, the peaks of GPC curve were merged. At the polymerization of $130^{\circ}C$, a unimodal GPC curve was shown. $Al(O-i-Pr)_3$ supported on amine-functionalized silica was able to produce higher MW PLA with enhanced activity compared to homogeneous $Al(O-i-Pr)_3$.

• Applied Chemistry for Engineering
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• v.10 no.7
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• pp.1028-1034
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• 1999

Poly(lactic acid) is expected to be one of the most promising biodegradable polymers. However, the high molecular weight polymer could be obtained by ring-opening polymerization process conventionally, which raises the production cost and decreases the final yield. In this study, linear and star-shaped poly(L-lactic acid)s were prepared by direct solution polycondensation method and their physical and thermal properties were examined. Tin compounds were found to be effective catalyst for the preparation of high molecular weight polymers. When 0.2g (0.5 wt % of monomer) of $SnCl_2$ and 100 mL of p-xylene were used, the polymer yield and molecular weight were relatively high. As a means to obtain higher molecular weight polymer easily in the direct polycondensation system, dipentaerythritol(dipet) or pentaerythritol(pet) was introduced as a multifunctional branching monomer to provide a star-shaped poly(lactic acid). Moderately high molecular weight polymers with the inherent viscosity values up to 1.14 dL/g(weight-average molecular weight of about 140000 by GPC) were obtained and could be cast strong and transparent films.

• Applied Chemistry for Engineering
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• v.23 no.4
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• pp.388-393
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• 2012

Branched polycarbonates (B-PCs) were synthesized using melt polymerization method with four different end capping agents and vaying concentrations. The chemical structure of the synthesized PC was determined by FT-IR and $^{1}H-NMR$ spectroscopy, and the reaction of the end capping agent was confirmed by the existence of hydroxy group in FT-IR spectrum. The average molecular weight and distribution, glass transition and degradation temperatures were determined by GPC, DSC and TGA. The average molecular weight changed with the chemical structure of end capping agent, and 4-tert-butylphenol was estimated as the optimum end capping agent. The average molecular weights of B-PCs decreased with the increase of the concentration of the agent, the number average molecular weight represented 20000 when 0.05 mol% of 4-tert-butylphenol was added to B-PCs. The melt viscosities of the B-PCs decreased with the decrease of the molecular weight of B-PCs, and adding of the agent was not effected to shear thinning tendency.