• Bulletin of the Korean Chemical Society
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• 제1권3호
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• pp.101-104
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• 1980

A sequential copolypeptide with repeating unit sequences, in which a glycyl residue is flanked progressively by two ${\gamma}$-benzyl-L-glutamyl residues, has been synthesized by poymerizing p-nitrophenyl ester of ${\gamma}$-benzyl-L-glutamyl-${\gamma}$ -benzyl-L-gutamyl-glycine. Polymers obtained were characterized by viscosity and infra-red spectral data. The highest molecular weight obtained was 21,000. Molecular conformation in solid state was found to be a mixed form of and |${\beta}$-structure. Polymers obtained were insoluble in the most of the organic solvents except in a strong acid like dichloroacetic acid, but in binary mixtures of solvents such as dichloroacetic acid-ethylene dichloride or dichloroacetic acid-chloroform, they were soluble within certain ranges of solvent compositions.

• Bulletin of the Korean Chemical Society
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• 제16권11호
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• pp.1109-1112
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• 1995

Bis(silyl)alkylbenzenes such as bis(1-sila-sec-butyl)benzene (1) and 2-phenyl-1,3-disilapropane (2) were prepared in high yields by reduction of the corresponding chlorosilanes with LiAlH4. The dehydropolymerization of 1 and 2 was carried out with group 4 metallocene complexes generated in situ from Cp2MCl2/Red-Al and Cp2MCl2/n-BuLi (M=Ti, Hf), producing two phases of polymers. The TGA residue yields of the insoluble polymers were in the range of 64-74%. The molecular weights of the soluble polymers produced ranged from 700 to 5000 (Mw vs polystyrene) and from 500 to 900 (Mn vs polystyrene). The dehydropolymerization of 1 and 2 seemed to initially produce a low-molecular-weight polymer, which then underwent an extensive cross-linking reaction of backbone Si-H bonds, leading to an insoluble polymer.

• Bulletin of the Korean Chemical Society
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• 제22권12호
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• pp.1337-1340
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• 2001

The bulk photopolymerization of methyl methacrylate (MMA) with para-substituted phenylsilanes such as F-C6H4SiH3 (1), H3C-C6H4SiH3 (2), and H3CO-C6H4SiH3 (3) was performed to produce poly(MMA)s containing the respective silyl moiety as an end group. For all the hydrosilanes, the polymerization yields and the polymer molecular weights decreased, whereas the TGA residue yields and the relative intensities of Si-H IR stretching bands increased as the relative silane concentration over MMA increased. The polymerization yields and polymer molecular weights of MMA with 1-3 increased in the order of 3 < 1 < 2. These hydrosilanes influence significantly upon the photopolymerization of MMA as both chain-initiation and chain-transfer agents.

• 폴리머
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• 제24권3호
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• pp.431-436
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• 2000

폴리락트산의 열적 안정성과 기계적 물성을 개선하고자 측쇄에 벤젠고리를 함유한 천연 $\alpha$-히드록시산인 만델린산(mandelic acid)과 L-락트산을 직접 용액 축중합법으로 공중합체를 합성하고 그 열적, 물리적 성질 등을 조사하였다. 합성된 공중합체는 무정형이었으며, 만델린산의 함량이 증가할수록 유리전이온도와 분해개시온도가 상승함을 열분석을 통해 알 수 있었다. 또한 만델린산을 5, 10 wt% 함유한 공중합체의 필름의 경우 그 기계적 성질이 다소 향상된 결과를 얻었다.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2008년도 춘계학술대회 논문집
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• pp.479-482
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• 2008

Since late of 2000, KIER has developed a novel pyrolysis process for production of fuel oils from polymer wastes. It could have been possible due to large-scale funding of the Resource Recycling R&D Center. The target was to develop an uncatalyzed, continuous and automatic process producing oils that can be used as a fuel for small-scale industrial boilers. The process development has proceeded in three stages bench-scale unit, pilot plant and demonstration plant. As a result, the demonstration plant having capacity of 3,000 tons/year has been constructed and is currently under test operation for optimization of operation conditions. The process consisted of four parts ; feeding system, cracking reactor, refining system and others. Raw materials were pretreated via shredding and classifying to remove minerals, water, etc. There were 3 kind of products, oils(80%), gas(15%), carbonic residue(5%). The main products i.e. oils were gasoline and diesel. The calorific value of gas has been found to be about 18,000kcal/$m^3$ which is similar to petroleum gas and shows that it could be used as a process fuel. Key technologies adopted in the process are 1) Recirculation of feed for rapid melting and enhancement of fluidity for automatic control of system, 2) Tubular reactor specially-designed for heavy heat flux and prevention of coking, 3)Recirculation of heavy fraction for prevention of wax formation, and 4) continuous removal & re-reaction of sludge for high yield of main product (oil) and minimization of residue. The advantages of the process are full automation, continuous operation, no requirement of catalyst, minimization of coking and sludge problems, maximizing the product(fuel oil) yield and purity, low initial investment and operation costs and environment- friendly process. In this presentation, background of pyrolysis technology development, the details of KIER pyrolysis process flow, key technologies and the performances of the process will be discussed in detail.

• 한국안광학회지
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• 제5권2호
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• pp.87-90
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• 2000

Poly(HEMA)는 소프트 콘택트렌즈의 재료로써 널리 사용되어 왔다. $phSiH_3$, $phMeSiH_2$, $ph2SiH_2$와 같은 다양한 hydrosilane들과 hydroxyethyl methacrylate(HEMA)와의 열중합은 Phenylsilyl 말단기를 포함하는 poly(HEMA)를 생성시켰다. 열중합 반응 동안에는 Phenylsilane의 농도가 증가함에 따라 고분자의 분자량과 고분자 수득률이 감소됨을 보였으며 광중합 반응에서 보다 중합 수득률, 고분자의 분자량, TGA 잔여 수율 등이 더 높았다.

• 한국재료학회지
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• 제2권1호
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• pp.35-42
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• 1992

실릴콘 산화막을 $CHF_3/C_2F_6$ 혼합가스를 사용하여 반응성이온 건식식각을 행할 때 실리콘 표면에 형성되는 잔류막과 손상충의 열적 거동을 X-선 광전자 분광기(XPS)와 이차이온 질량 분석기 (SIMS)를 사용, 연구하였다. 저항가열을 통한 in-situ 분석에 의해 폴리머 잔류막은 $200^{\circ}C$부터 분해가 시작되고 $400^{\circ}C$ 이상의 가열에서는 graphite 형태의 탄소 결합체를 형성하며 분해됨을 알았다. 질소 분위기하의 급속 열처리를 통해 잔류막의 열분해는 $800^{\circ}C$ 이상에서 완료되고 손상층을 형성하는 침투 불순원소의 기판 외부로의 확산이 관찰되었다.

• 폴리머
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• 제36권3호
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• pp.315-320
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• 2012

아크릴 공중합체의 구조와 다관능성 단량체의 관능성 및 함량을 조절하여 반도체 제조공정에 적합한 자외선 경화형 점착제를 제조하였다. 아크릴 공중합체는 점착력을 부여하는 기본수지로 사용되었고 다관능성 단량체는 광가교 특성으로 인하여 3차원 가교구조와 가교밀도를 변화시키기 위해 사용하였다. 아크릴 공중합체는 단량체 조성에서 2-ethylhexyl acrylate의 함량이 감소할수록 자외선 조사 후의 박리 점착력이 감소하였다. 광경화 특성을 갖는 다관능성 단량체의 탄소 이중결합 관능성이 증가할수록 자외선 조사 후 가교밀도가 증가하여 박리 점착력이 감소하였고 박리 후 웨이퍼 표면에 남게 되는 점착제 잔사물도 크게 감소하였다. 6관능성 단량체를 20 phr 포함하는 광가교형 감압점착제가 자외선 조사 전 점착력이 높고, 자외선 조사 후 박리 점착력이 낮고, 박리 후 웨이퍼 표면에 남게 되는 점착제 잔사물이 가장 적었다.

• 폴리머
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• 제32권2호
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• pp.125-130
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• 2008

A commercial cyclic diphosphonate ester (TPMP) and melamine (MA) was combined and added to polyamide 6 (PA6) to prepare the fire retardant PA6. An increase of the oxygen index to 28.6 as well as an improvement of the UL-94 classification to V-0 rating was observed. Cone measurements explained the rate of heat release (RHR) decreased and TGA showed the early decomposition and high solid residue due to co-addition of TPMP and MA, suggesting the occurrence of synergistic effect of TPMP and MA on fire resistance of PA6. The morphology of the char developed during combust ion showed the appearance of thick, intumescent cells on the surface of retardant PA6, which protects the underlying material from the action of the heat flux or flame and limits the diffusion of combustible volatile products towards the flame and oxygen.

• 한국고분자학회:학술대회논문집
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• 한국고분자학회 2006년도 IUPAC International Symposium on Advanced Polymers for Emerging Technologies
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• pp.139-140
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• 2006

Some of novel halogen-free, elastomeric flame retardants for nylon-6 have been developed. It is found that the S-ENP and clay have a synergistic flame retardant effect on nylon-6 resulted from the formation of two barriers on the nanocomposite residue surface at the end of combustion. A novel flame retardant ternary nanocomposite of nylon-6/ENP/nano-Magnesium hydroxide was also fabricated. The new ternary composite has better flame retardancy and thermal stability than the conventional one because nano-MH can disperse much more homogeneous in the new ternary composite than in the conventional one.