• 전기학회논문지
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• 제61권9호
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• pp.1362-1367
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• 2012

High porous silica aerogel/polyurethane polymer composite was manufactured by cross-linking polymerization of polyurethane foaming process. The properties of microstructure, mechanical strength, and thermal properties were investigated for its various applications. The superhydrophobic silica aerogel powders were used for highly thermal insulation filler materials. The thermal conductivities can be resulted 0.07 W/mK to 0.13 W/mK, by decreasing the contents of silica aerogels in composite materials. It is found that the polymerization formulation by organic binders can be applied to heavy industires, building materials, and various industries.

• Macromolecular Research
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• 제17권11호
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• pp.926-930
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• 2009

A new method for encapsulating nanomaterials within intermediary layer cross-linked (ILCL) polymeric micelles using a bifunctional photo-cross-linking agent was developed. For ILCL polymeric micelles, an amphiphilic triblock copolymer of poly(ethylene glycol)-b-poly(2-hydroxyethyl methacrylate)-b-poly(methyl methacrylate) (PEG-PHEMA-PMMA) was synthesized via consecutive atom transfer radical polymerization (ATRP), Di(4-hydroxyl benzophenone) dodecanedioate (BPD) was used as a bifunctional photo-cross-linking agent. The PMMA-tethered Au nanoparticles and BPD, or pyrene and BPD were encapsulated in the PEG-PHEMA-PMMA micelles, and their intermediary layers were photo-cross-linked by UV irradiation for 1 h. The HEMA units donated labile hydrogens to the excited-state benzophenone groups in BPD, and they were subsequently cross-linked by BPD through radical-radical combination. The spherical structures of the PEG-PHEMA-PMMA micelles containing the Au nanoparticles or pyrene were unaffected by the photo-cross-linking process.

• 한국응용과학기술학회지
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• 제21권4호
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• pp.370-379
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• 2004

Highly crosslinked micron-size monodispersed PMMA/PDVB and PS/PDVB particles were prepared using seeded multi-stage emulsion polymerization. PMMA and PS seed particles were synthesized by seeded multi-stage emulsion polymerization and soap-free emulsion polymerization. Then PMMA/PDVB and PS/PDVB particles were obtained using semi-batch type emulsion polymerized using divinyl benzene as a cross-linkable monomer in the presence of seed particles. PMMA particles with size of ca. 730 nm and polydispersity of 1.03 were successfully prepared in this experiment. PS particles with size of ca. 1.5 ${\mu}m$ and polydispersity of 1.01 were prepared in this experiment. Highly crosslinked PS/PDVB particles with size of ca. 1.3 ${\mu}m$ and polydispersity of 1.00 were obtained.

• Bulletin of the Korean Chemical Society
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• 제29권10호
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• pp.1941-1945
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• 2008

A new chromatographic stationary phase has been prepared by cross polymerization between allylsilica and perallyloxycucurbit[6]uril and characterized by elemental analysis and FT-IR spectroscopy. The double endcapping has been proven to improve the separation efficiency of the cucurbituril-based stationary phase material. The first end-capping was carried out when allylsilica was made. The second end-capping was done as the final step of the whole process, and the use of a mixture of hexamethyldisilazane (HMDS) and trimethylchlorosilane (TMCS) as an end-capping reagent was found better than the use of only HMDS or TMCS. Our stationary phase has shown generally good results in separation of nonpolar and polar analytes. This phase showed even better separation performance than the commercial C18 phase for the case where hostguest chemistry was properly incorporated in solute retention.

• 멤브레인
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• 제19권4호
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• pp.333-340
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• 2009

본 연구의 목적은 중금속 흡착을 위한 방사선 그라프트 중합법에 의한 이온교환막의 성능 향상을 위한 것이다. 그라프트 체인의 이온교환기에 의해 체인이 막의 pore를 방해하여 투과유속이 크게 저하되는 문제를 해결하고자 그라프트 체인과 체인사이를 N-ethyleneglycoldimethacrylate계 가교제를 첨가하여 투과유속이 저하되는 문제를 해결하고자 했다. 이때 사용된 가교제는 길이가 서로 다른 ethylene glycol dimethacrylate (EDMA)와 diethylene glycol dimethacrylate (DDMA)를 사용하였다. GMA 막에 가교제가 첨가된 이온교환막에 술폰산기를 첨가한 막을 이용하여 중금속 이온($Pb^{2+}$) 흡착을 하였다. 술폰산기 밀도가 1.40 mmol/g인 EDMA막은 13.82 mg/g을 흡착하였고, 술폰산기 밀도가 2.14 mmol/g인 DDMA막은 17.37 mg/g의 흡착량을 보였다.

• 한국응용과학기술학회지
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• 제36권1호
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• pp.305-311
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• 2019

높은 함수율을 갖는 소프트렌즈를 제조하기 위하여 아크릴계 공중합체를 설계, 제조하였다. 공중합체용 모노머로 2-hydroxyethyl methacrylate(HEMA)를 사용하였고 가교제로는 ethylene glycol dimethacrylate(EGDMA), glycerol dimethacrylate(GD) 혹은 glycerol 1,3-diglycerolate diacrylate(GDD)를 이용하여 렌즈를 제조하였다. 함수율 측정결과, 고함수율 렌즈는 기존의 36%에서 46%로 높게 나타났으며 접촉각도 38.6 에서 34.4 로 낮아져 표면 친수성이 높게 나타남을 확인하였다. 인장강도는 가교제의 친수성이 증가함에 따라 0.1MPa 에서 0.08 그리고 0.05 로 감소하였고 전자현미경으로 렌즈의 단면을 확인한 결과 상분리 현상은 나타나지 않았다. 광중합은 Real-time infrared(RTIR)로 측정하였는데 초기 중합 속도가 가교제에 따라 0.6 에서 0.9 로 나타났다.

• 한국진공학회지
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• 제6권3호
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• pp.213-219
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• 1997

본 연구에서는 내전극 정전결합 유동가스형 반응장치를 이용하여 플라즈마 중합 스 티렌 박막을 제작하고 적외선분광스펙트럼, 열분해가tm크로마토그래피, 시차주사열량계 및 겔투과성 크로마토그래피의 분석을 통하여 중합조건이 분자구조 및 분자량 분포에 미치는 영향을 조사하였다. 위의 결과로부터 개시 모노머의 화학적 특성과는 다른 고도로 가교된 박막이 생성되었으며, 방전압력, 방전전력 및 가스의 유량 등의 중합조건 조절에 의해 분자 구조, 가교도, 분자량 분포 등의 제어가 가능함이 판명되었다. 따라서 내전극 정전결합 유동 가스형 반응장치에 의해 수행된 플라즈마중합법은 중합조건의 조절에 의해 센서의 감지막, 광도전성 소자 및 포토 레지스트 등에 응용가능한 기능성 유기박막의 제작에 좋은 특성을 나타내는 것을 알 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제18권3호
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• pp.318-323
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• 1997

ο-(2-Vinyloxyethoxy)benzylidenemalononitrile (3a) and methyl ο-(2-vinyloxyethoxy)-benzylidenecyanoacetate (3b), m-(2-vinyloxyethoxy)benzylidenemalononitrile (4a), and methyl m-(2-vinyloxyethoxy)benzylidenecyanoacetate (4b) were prepared by the condensation of ο-(2-vinyloxyethoxy)benzaldehyde (1) and m-(2-vinyloxyethoxy)benzaldehyde (2) with malononitrile or methyl cyanoacetate, respectively. Bifunctional vinyl ether monomers 3a and 3b polymerized quantitatively with radical initiators in γ-butyrolactone solution at 65 ℃, while meta-isomers 4a and 4b gave lower yields of polymers under the same conditions. The polymers 5-6 obtained from the monomers 3-4 were insoluble in common solvents due to cross-linking. Under the same polymerization conditions ethyl vinyl ether polymerized well with model compounds ο-methoxybenzylidenemalononitrile 7a, methyl ο-methoxybenzylidenecyanoacetate 7b, m-methoxybenzylidenemalononitrile 8a, and methyl m-methoxybenzylidenecyanoacetate 8b, respectively, to give 1:1 alternating copolymers 9-10 in high yields. Cross-linked polymers 5-6 showed a thermal stability up to 300 ℃, and showed a double phase degradation pattern in their TGA thermograms. Polymers 5-6 showed broad endothermic bands around 75-110 ℃ without any characteristic Tg peaks in DSC thermograms. Alternating copolymers 9-10, except copolymer 9b were soluble in common organic solvents. The inherent viscosities of polymer 9-10 were in the range of 0.35-0.62 dL/g. Polymer films cast from acetone solution were cloudy and tough and Tg values obtained from DSC thermograms were in the range of 118-165 ℃.

• 대한소아치과학회지
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• 제25권2호
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• pp.368-382
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• 1998

The purpose of this study is to evaluate and compare the results of argon laser for 5 seconds, argon laser for 10 seconds, and visible light for 40 seconds photo-polymerization in compressive strength, microhardness, curing depth, temperature rising during polymerization, and polymerization shrinkage. Hybrid type composite resin(Z-100) and compomer(Dyract) were used to be compared. The compressive strength was measured by an Instron(1mm/min cross head speed) in 60 specimens and the microhardness of the surface was expressed by Vickers Hardness Number(VHN) in 30 specimens. The curing depth was evaluated comparing the different values of upper and lower VHN according to irradiation time and thickness for the light source polymerization in 60 specimens. The temperature rising during photopolymerization was observed by the temperature change with thermocouple sensitizer beneath 40 specimens at the argon laser for 10 seconds and visible light 40 seconds irradiation. The polymerization shinkage was evaluated by calculating the decrease of % volume by using a dilatometer in 30 specimens. The results were as follows ; 1. In the case of compressive strength, the argon laser polymerization groups were higher than visible light group in Z-100 (p<0.05). In Dyract, the argon laser 5 seconds group did not show a significant difference with the visible light 40 seconds group. The argon laser 10 seconds group showed the markedly low value when compared with other groups (p<0.05) 2. In microhardness, Z-100 was better than Dyract when comparing by VHNs (p<0.05); however, there was not a significant difference between two materials in the visible light 40 seconds group and the argon laser 10 seconds group. 3. In the study of curing depth, Z-100 showed the consistent polymerization in argon laser irradiation because there was no difference in the VHN decrease according to the thickness change. Over the thickness control, the results did not show a significant difference between visible light and argon laser group in Z-100; however, in the case of Dyract, the visible light 40 seconds group was better than the argon laser groups(p<0.05). 4. There was a significant difference between the two materials in temperature rising during polymerization (p<0.05), but not a significant difference between irradiation times, 5. There was not a significant difference between the two materials in polymerization shrink age. The argon laser 5 seconds group was smaller than the other groups (p<0.05). It could be concluded that Z-100 polymerization was recommended to use the argon laser for reduction of the irradiation time while Dyract was recommended to use the visible light polymerization.

• 공업화학
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• 제17권1호
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• pp.33-36
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• 2006

광경화 접착제로 많이 사용되는 우레탄-아크릴레이트 올리고머의 광경화 거동을 자체촉매화 반응모델식을 통해 중합온도 및 올리고머의 관능성에 따른 영향을 확인하여 보았다. 중합온도가 증가함에 따라 최대중합속도는 감소하여 중합온도가 경화 거동에 대한 영향인자임을 확인할 수 있었으며, 반응속도상수 k는 온도증가에 따라 거의 일정한 값을 보이나 반응차수 m과 n은 증가하는 경향을 보였는데 이는 가교구조에 의한 반응성 기의 확산제한 및 유동성의 제한으로 인한 것으로 판단되어진다. 온도증가에 따른 중합속도의 감소는 주로 반응차수 n의 증가에 의해 진행되었다.