• 한국염색가공학회지
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• 제2권4호
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• pp.223-230
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• 1990

This study was carried out with the view of fundamental investigating to improve the tactile and the hygroscopicity of Poly (ethylene terephthalate) (PET) fibers. Mono-sodium ethylene glycolate in ethylene glycol (MSEG-EG) solution was prepared and PET films were treated with it. The following conclusions were obtained. 1. The tensile strength decreased with increasing decomposition ratio while density, crystallinity and crystallite size increased with increasing decomposition ratio when PET films were treated with MSEG-EG solution. 2. Number of carboxyl end groups was increased until 10-20% decomposition ratio when PET films were treated with MSEG-EG solution. However, the decomposition ratio became more than 20%, the number of carboxyl end groups had tendency to decreased. 3. The surface tension of PET films increased for treating with MSEC-EG solution. Hydrogen bonding force and poler force among the components of surface tension increased while dispersion force among those decreased. 4. The moisture region of PET films increased with increasing decomposition ratio when PET films were treated with MSEG-EG solution.

• 한국가축번식학회지
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• 제8권1호
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• pp.22-28
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• 1984

This experiment was carried out to investigate effects of DMSO or ethylene glycol as a cryopotectant and of freezing methods on survival rate of forozen-thawed rat 2-cell embryos by morphological observation. 2-cell embryos were recovered from oviducts of Sprague Dawley females mated with males of same strain on day 2 of pregnancy after inducing superovulation by intrapertioneal injection of PMSG and HCG. In slow freezing and thawing groups, embryos were frozen to -79$^{\circ}C$ or -196$^{\circ}C$ in a glass test tube containing 0.2ml PBI with 1.5M DMSO or 1.2M ethylene glycol at a rate of 0.3-1.0C/min. and thawed slowly. When samples were frozen to -79$^{\circ}C$, higher survival rate was obtained in the medium containing DMSO (43.9%) than ethylene glycol (41%). And similar result was obtained (32.5% in DMSO vs. 31.4% in ethylene glycol) when samples were frozen. In rapid freezing and thawing groups, embryos were frozen to -79 or -196$^{\circ}C$ in a glass test tube containing 0.2ml of PBI with 1.5M DMSO or 1.2M ethylene glycol by rapid cooling, and thawed rapidly. When samples were frozen to -79$^{\circ}C$, 1.5M DMSO (13.2%) was more effective than 1.2M ethylene glycol (6.1%). When the storage temperature was -196$^{\circ}C$, survival rates were 9.8% in 1.5M and 5.4% in 1.2M ethylene glycol.

• 한국식품저장유통학회지
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• 제5권1호
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• pp.29-34
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• 1998

This study was carried out to investigate the effects of calcium and galactose treatments on ethylene productions in persimmon fruits for the study on the study of persimmon fruits. Ethylene was producted in green mature persimmon fruits treated with water, calcium and galactose after 24hrs of treatment. Ethylene productions of persimmon fiuits treated with galactose was very higher than those of persimmon fruits treated with water and calcium after 72hrs of treatment. Ethylene productions of persimmon fruits teated with water and calcium were similarly to that of persimmon fruit tested with calcium. The treatment of glucose was not effected on ethylene production of persiommn fruits. The ACC contents and ACC synthase activity in persimmon fruit treated with galactose were higher than those of other groups after 72hrs of storage, but the ACC contents and ACC synthase activity of persimmon fruits treated with calcium were lower than those of control and persimmon fruits treated with water.

• Fibers and Polymers
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• 제2권2호
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• pp.86-91
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• 2001

Liquid crystalline (LC) poly(ethylene terephthalate-co-2(3)-chloro-1,4-phenylene terephthalate) [copoly(ET/CPT)] was prepared using poly(ethylene terephthalate) (PET) as a flexible spacer, terephthalic acid (TPA), and chlorohydroquinone diacetate (CHQDA). All reactions involved in the copolymerization were investigated using some model compounds: TAP was used for acidolysis, diphenylethyl terephthalate (DPET) for interchange reaction between PET chains, and 야-o-chlorophenyl terephthalate (DOCT) and di-m-chlorophenyl terephthalate (DMCT) for interchange reaction between PET and rigid rodlike segments. Activation energies obtained for the acidolysis of PET with TPA and for interchange reaction of PET with DPET, DOCT, and DMCT were 19.8 kcal/mol, 26.5 kcal/mole, and 45.9 kcal/mole, respectively. This result supports that the copolymerization proceeds through the acidolysis of PET with TPA first and subsequent polycondensation between carboxyl end group and CHQDA or acetyl end group, which is formed from the reaction of CHQDA and TPA. Also, it was found that ester-interchange reaction can be influenced by the steric hindrance. Copoly(ET/CPT)s obtained has ethylene acetate end groups formed from acetic acid hydroxy ethylene end groups and showed almost the random sequence distribution for all compositions.

• 대한의용생체공학회:의공학회지
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• 제12권1호
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• pp.57-62
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• 1991

ABA type block copolymers composed of poly($\gamma-benzyl$ L-glutamate) (PBLG) as the A component and poly (ethylene glycol) as the B component were obtained by polymerization of $\gamma-benzyl$ L-gletamate N -carboxyanhydride, initiated by amino groups at both ends of poly(ethylene glycol) . From circular dichroism measurements in ethylene dichloride solution as well as from infrared spectTa measurements in solid state, it was found that the polypep- tide block exists in the a-helical conformation, as in PBLG homopolymer. $Poly-N^5$ (3-hydroxypropyl glutamine) (PHPG)/poly(ethylene glycol)block copolymer hydrogel was obtained by the treatment of PBLG/PBG block copolymer with the mixture of 3-ammine-1-propanol and diamlnooctane. The water content of PHPG/PEG block copolymer hydrogel was about 80wt% when the concentration of crosslinking agent was below 5 mole % per polymer.

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 2003년도 가을 학술발표회 논문집
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• pp.167-168
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• 2003

Dimethyl-2,6-naphthalenedicarboxylate(2,6-NDC)와 ethylene glycol(EG)로부터 유도되는 폴리에틸렌 나프탈레이트(PEN)는 폴리에틸렌 테레프탈레이트(PET)보다 열적 및 기계적 특성이 우수한 열가소성 고분자이며[1-2], 폴리에틸렌 글리콜(PEG)은 diol기를 함유한 친수성 고분자로서 의약품 및 기타 가공제로 널리 쓰이는 물질이다. 이미 PET는 이러한 PEC를 PET 합성과정에서 공단량체로 사용해 공중합시킴으로서 친수성을 갖는 PET로 개질하고자 하는 연구[3-4]가 다수 보고되어 왔으나, PEN의 경유는 아직 이에 관한 연구보고가 없는 실정이다. (중략)

• 폴리머
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• 제36권6호
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• pp.822-830
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• 2012

본 연구에서는 실리카 나노입자를 우수한 내가수분해성을 가지는 dipodal 형태의 bis[3-(trimethoxysilyl)propyl]amine(BTMA) 실란 커플링제로 표면 개질한 후, 실리카에 도입된 BTMA의 2차 아미노기인 N-H기와 마이클 부가반응이 가능한 acrylate기를 1분자당 2개씩 가지는 poly(ethylene glycol)diacrylate(PEGDA)로 표면 처리하여 acrylate기를 실리카 입자 표면에 도입하는 연구를 수행하였다. PEGDA의 몰수 및 3가지 서로 다른 분자량의 PEGDA(M.W. 258, 575, 700) 처리가 실리카 표면에 도입되는 acrylate기의 구조에 미치는 영향을 fourier transform infrared spectroscopy(FTIR), elemental analysis(EA, 원소분석) 및 고체 상태 $^{13}C$ cross-polarization magic angle spinning(CP/MAS) nuclear magnetic resonance spectroscopy(NMR)법을 사용하여 분석하였다. 액체상태의 순수 PEGDA와 순수 BTMA를 같은 몰 비로 반응시키면 PEGDA 1분자당 2개씩 존재하는 acrylate기 중 1개 acrylate기는 순수 BTMA의 N-H기와 1:1의 비율로 마이클 부가반응이 일어나 ${\beta}$-amino acid ester를 형성하고, 나머지 1개의 acrylate기는 남아서 중합반응이 가능한 단량체 합성이 가능하다. 하지만, BTMA로 개질된 실리카 입자를 PEGDA와 반응시키면, PEGDA 1분자당 2개씩 결합있는 acrylate기 대부분이 실리카 입자에 결합되어 있는 BTMA의 N-H기와 마이클 부가반응으로 ${\beta}$-amino acid ester를 형성하여, acrylate기의 C=C기 대부분이 C-C로 변화함을 확인하였다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2016년도 제50회 동계 정기학술대회 초록집
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• pp.376-376
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• 2016

Poly(ethylene oxide) (PEO)/functionalized bacterial cellulose nanowhiskers (f-BCNW) (0.1 wt%) composite nanofibers were fabricated by electrospinning process and the thermomechanical properties were significantly enhanced more than the PEO and PEO/bacterial cellulose nanowhiskers (BCNW) (0.1 wt%) composite nanofibers. The functionalization of BCNW (f-BCNW) was performed by microwave plasma treatment for effects of nitrogen functionalization of chemically-driven BCNW. The N-containing functional groups of f-BCNW enhanced chemical bonding between the hydroxyl groups of the polymer chains in the PEO matrix and diameter size of PEO/f-BCNW (0.1 wt%) composite nanofibers were decreased more than PEO and PEO/BCNW (0.1 wt%) composite nanofibers on the same concentration. The strong interfacial interactions between the f-BCNW nanofillers and polymer matrix were improved the thermomechanical properties such as crystallization temperature, weight loss and glass transition temperature (Tg) compared to PEO and PEO/BCNW composites nanofibers. The results demonstrated that N2 plasma treatment of BCNW is very useful in improving thermal stability for bio-applications.

• 한국염색가공학회지
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• 제21권5호
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• pp.16-20
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• 2009

Films of Poly(ethylene oxide), PEO, were modified to impart hydrophilicity via UV irradiation. The UV irradiation treatment produced new photo-oxidized groups of carbonyl and ether groups as indicated in ATR and ESCA analysis. It was found that water contact angle decreased from $15^{\circ}C$ to $10^{\circ}C$ and total surface energy of PEO increased from 54.2 mN/m to 76.6 mN/m with increasing UV energy, which was attributed to significant contribution of acid base interaction of the photo-oxidized PEO rather than nonpolar interaction originating from the dominant increase in Lewis acid parameter. The increased hydrophilicity and surface energy were also proved by the decreased water wetting time.

• Macromolecular Research
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• 제9권6호
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• pp.332-338
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• 2001

Waterborne polyurethane as a new polymer electrolyte was synthesized by using relatively hydrophilic polyols. The morphology of polyurethane was changed as it was dispersed in water. In contrast to polyurethane ionomer, waterborne polyurethane did not form an ionic cluster but produced a binary system composed of hydrophilic and hydrophobic groups. In the colloidal system, the former and the latter existed at outward and inward, respectively. Waterborne polyurethane was prepared from poly(ethylene glycol) (PEG) /poly(propylene glycol) (PPG) copolymer, 4,4'-diphenylmethane diisocyanate(MDI), ethylene diamine as a chain extender, and three ionization agents, 1,3-propane sultone, sodium hydride and lithium hydroxide. PEG/PPG copolymer was used for suppressing the crystallinity of PEG and N-H bond was ionized for increasing the electrochemical stability of polyurethane. Low molecular weight poly(ethylene glycol) and poly(ethylene glycol dimethyl ether) (PEGDME) were used as plasticizers. DSC, FT-IR and $^1$H-NMR of the waterborne polyurethane were measured. Also, the ionic conductivity of solid polymer electrolytes based on waterborne polyurethane and various concentrations of low molecular weight poly(ethylene glycol) or PEGDME were measured by AC impedance.