• Restorative Dentistry and Endodontics
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• 제26권5호
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• pp.393-398
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• 2001

Polymerization of light-activated restorations results in temperature increase caused by both the exothermic reaction process and the energy absorbed during irradiation. Within composite resin, temperature increases up to 2$0^{\circ}C$ or more during polymerization. But, insulation of hard tissue of tooth lowers this temperature increase in pulp. However, many clinicians are concerned about intrapulpal temperature injury. The purpose of this study was to evaluate temperature changes in the pulp according to various restorative materials and bases during curing procedure. Caries and restoration-free mandibular molars extracted within three months were prepared Class I cavity of 3$\times$6mm with high speed handpiece fissure bur. 1mm depth of dentin was evaluated with micrometer in mesial and distal pulp horns. Pulp chambers were filled with 37.0$\pm$0.1$^{\circ}C$ water to CEJ. Chromium-alumina thermocouple was placed in pulp horn below restorative materials for evaluating of temperature changes. This thermocouple was connected to temperature-recording device(Multiplication analyzer MX, 6.000, JAPAN). Temperature changes was evaluated from initial 37.$0^{\circ}C$ after temperature changes to 37.$0^{\circ}C$. Tip of curing unit was placed in the center of prepared cavity separated 1mm from restorative materials. Curing time was 40s. The restorative materials were used with Z 100, Fuji II LC, Compoglass flow and bases were used with Vitrebond, Dycal. Resrorative materials were placed in 2mm. The depth of bases were formed in 1mm and in this upper portion, resin of 2mm depth was placed. This procedure was performed 10 times. The results were as follows. 1. All the groups showed that the temperature in pulp increased as curing time increased 2. The temperature increase of glass ionomer was significantly higher than that of Resin and Compomer during curing procedure (P<0.05). 3. The temperature increase in glass ionomer base was significantly higher than that of Calcium hydroxide base during Resin curing procedure (P<0.05).

• 한국막학회:학술대회논문집
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• 한국막학회 1998년도 춘계 총회 및 학술발표회
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• pp.99-101
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• 1998

1. Introduction : The conventional grafting polymerization technique requires chemically reactive groups on the surface as well as on the polymer chains. For this reason, a series of prefunctionalization steps are necessary for covalent grafting. The surface prefunctionalizational technique for grafting can be used to ionization radiation, UV, plasma, ion beam or chemical initiators. Of these techniques, radiation method is one of the useful methods because of uniform and rapid creation of active radical sites without catalytic contamination in grafted samples. If the diffusion of monomer into polymer is large enough to come to the inside of polymer substrate, a homogeneous and uniform grafting reaction can be carried out throughout the whole polymer substrate. Radiation-induced grafting method may attach specific functional moieties to a polymeric substrate, such as preirradiation and simultaneous irradiation. The former is irradiated at backbone polymer in vacuum or nitrogen gas and air, and then subsequent monomer grafting by trapped or peroxy radicals, while the latter is irradiated at backbone polymer in the presence of the monomer. Therefore, radiation-induced polymerization can be used to modification of the chemical and physical properties of the polymeric materials and has attracted considerable interest because it imparts desirable properties such as blood compatibility. membrane quality, ion excahnge, dyeability, protein adsorption, and immobilization of bioactive materials. Synthesizing biocompatible materials by radiation method such as preirradiation or simultaneous irradiation has often used $\gamma$-rays to graft hydrophilic monomers onto hydrophobic polymer substrates. In this work, in attempt to produce surfaces that show low levels of anti-fouling of bovine serum albumin(BSA) solutions, hydroxyethyl methacrylate(HEMA) was grafted polypropylene membrane surfaces by preirradiation technique. The anti-fouling effect of the polypropylene membrane after grafting was examined by permeation BSA solution.

• Membrane and Water Treatment
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• 제9권4호
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• pp.211-220
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• 2018

Incorporating nano-materials in thin-film composite (TFC) membranes has been considered to be an approach to achieve higher membrane performance in various water treatment processes. This study investigated the rejection efficiency of three target compounds, i.e., reserpine, norfloxacin and tetracycline hydrochloride, by TFC membranes with different graphene oxide proportions. Graphene oxide (GO) was incorporated into the polyamide active layer of a TFC membrane via an interfacial polymerization (IP) reaction. The TFC membranes were characterized with FTIR, FE-SEM, AFM; in addition, the water contact angle measurements as well as the permeation and separation performance were evaluated. The prepared GO-TFC membranes exhibited a much higher flux ($3.11{\pm}0.04L/m2{\cdot}h{\cdot}bar$) than the pristine TFC membranes ($2.12{\pm}0.05L/m2{\cdot}h{\cdot}bar$) without sacrificing their foulant rejection abilities. At the same time, the GO-modified membrane appeared to be less sensitive to pH changes than the pure TFC membrane. A significant improvement in the anti-fouling property of the membrane was observed, which was ascribed to the favorable change in the membrane's hydrophilicity, surface morphology and surface charge through the addition of an appropriate amount of GO. This study predominantly improved the understanding of the different PA/GO membranes and outlined improved industrial applications of such membranes in the future.

• 대한화학회지
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• 제24권2호
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• pp.155-166
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• 1980

3-(N-Carbonylpyrrolidone)-propanoic acid의 potassium-salt와 3-N-carbonyrrolidone)-propenoic acid의 potassium-salt를 합성하고 이것을 2-pyrrolidone 음이온중합의 개시제로 사용하여 그 효과를 조사하였다. $50^{\circ}C$에서 KOH의 농도를 2mole%로 고정시키고, 개시제를 1.5, 1.0, 0.5mole%로 변화시켰을때 1.0mole%에서 좋은 결과를 얻을 수 있었다. 3-(N-Carbonylpyrrolidone)propenoic acid K-salt/KOH catalysis에 의하여 합성한 nylon 4의 inherent viscosity는 2.3dl/g이였고 3-(N-carbonylpyrrolidone)-propanoic acid K-salt 개시제에 의하여 합성한 중합체의 ingerent viscosity는 1.2dl/g이었다.

• 폴리머
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• 제35권3호
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• pp.244-248
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• 2011

Copper(I) chloride와 아빈 계열의 리간드와의 Cu-amine complex 촉매를 사용한 단량체 2,6-dimethlyphenol (DMP)의 산회중합을 통하여 poly (2,6-dimethyl-1,4-phenylene ether) (PPE)를 제조하였다. 중합반응에 있어서 DMP와 촉매의 비율, 다양한 리간드 및 첨가제로서 2,4,6-trimethylphenol(TMP)의 함량 등 여러 반응 변수들의 영향을 분자량측정, 열분석, 및 광학적 특성분석을 통해 조사하였다. DMP의 산화중합에 사용된 다양한 Cu-amine 촉매 system의 중합활성을 비교하기 위하여 oxygen-uptake 실험을 실시하였다. 또한 제조된 PPE의 EDTA 수용액을 사용한 정제 방법을 통하여 잔류촉매 제거가 PPE의 열 안정성에 미치는 효과를 TGA를 통해 확인하였다.

• 폴리머
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• 제32권6호
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• pp.549-554
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• 2008

분산중합법에 의해 고분자 미립자를 합성하기 위해 스티렌과 n-butylmethacrylate가 알루미나와 함께 중합되었다. 스티렌과 n-butylmethacrylate의 비는 3 : 1이었고, 입자안정제는 poly (N-vinyl pyrrolidon), 중합 개시제로는 2,2'-azobis(isobutyronitrile)를 커플링제는 3-methacryloxypropyl trimethoxysilane을, 분산매로 이소프로판올과 이온교환수를 70 : 30의 비로 사용하였다. TEM 사진을 통해 알루미나가 고분자 미립자에 분산되어 있음을 확인하였고 알루미나의 농도가 증가함에 따라 평균 입자경이 증가하였으며 입자경 분포는 감소되는 경향을 보였다. XRD 측정에 의해 알루미나의 농도 증가는 피크 강도와 2$\theta$값의 증가를 보였으며 TGA 측정으로 알루미나의 농도의 증가는 고분자 미립자의 내열성을 증가시킴을 알 수 있었다. 사용한 개시제의 반감기가 길수록 입자경은 감소하였고 입자인정제의 농도가 증가할수록 반응초기의 핵생성이 증가하여 입자경이 또한 감소함을 알 수 있었다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2009년도 제38회 동계학술대회 초록집
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• pp.458-458
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• 2010

The process window for the etch selectivity of silicon nitride ($Si_3N_4$) layers to extreme ultra-violet (EUV) resist and variation of line edge roughness (LER) of EUV resist were investigated durin getching of $Si_3N_4$/EUV resist structure in a dual-frequency superimposed capacitive coupled plasma (DFS-CCP) etcher by varying the process parameters, such as the $CH_2F_2$ and $N_2$ gas flow rate in $CH_2F_2/N_2$/Ar plasma. The $CH_2F_2$ and $N_2$ flow rate was found to play a critical role in determining the process window for infinite etch selectivity of $Si_3N_4$/EUV resist, due to disproportionate changes in the degree of polymerization on $Si_3N_4$ and EUV resist surfaces. The preferential chemical reaction between hydrogen and carbon in the hydrofluorocarbon ($CH_xF_y$) polymer layer and the nitrogen and oxygen on the $Si_3N_4$, presumably leading to the formation of HCN, CO, and $CO_2$ etch by-products, results in a smaller steady-state hydrofluorocarbon thickness on $Si_3N_4$ and, in turn, in continuous $Si_3N_4$ etching due to enhanced $SiF_4$ formation, while the $CH_xF_y$ layer is deposited on the EUV resist surface. Also critical dimension (and line edge roughness) tend to decrease with increasing $N_2$ flow rate due to decreased degree of polymerization.

• 한국식품과학회지
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• 제28권1호
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• pp.146-151
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• 1996

6종류의 알긴산을 기질로하여 효소 반응을 시켜 알긴산 올리고당 제조를 시도한 결과, 실험에 사용한 효소의 경우 G-rich block에만 특이하게 작용하는 guluronate lyase 일종으로 G-block에 주로 작용하여 올리고당을 생성하는 것으로 확인되었다. 또한 4종류의 시판 알긴산중에서도 1종(Wako Co.)의 Na-alginate에 대해서 특이하게 6-7개의 올리고당 spot가 TLC에서 확인되었고, 그외 3종의 Na-alginate는 2-4개 정도의 올리고당 spot가 TLC에 나타났다. 6-7개의 spot가 확인된 Na-alginate(Wako Co.)를 기질로 대량 분해시킨 후 Sephadex G-25 및 Bio-gel p-2로 분획, 정제를 행하고 중합도를 측정하여 올리고당을 확인한 결과, 중합도가 각각 다른 4개의 올리고당을 확인할 수 있었다.

• 대한화장품학회지
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• 제36권1호
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• pp.17-32
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• 2010

본 총설에서는 이산화탄소에 용해력이 있는 새로운 탄화수소 공중합체의 설계와 개발, 그리고 생체친화성 고분자의 초임계 중합을 위한 효과적인 계면활성제로써의 성능에 대해 소개하고, 초입계 유체의 기본적 개념을 용매로서의 성질과 고분자 합성분야에서의 응용적인 측면에서 기술한다. 이산화탄소에 높은 용해력을 지닌 탄화수소 고분자 중합을 위해 새로운 리빙라디칼 중합기술을 사용하였고, 이 물질들의 이산화탄소 내에서의 상거동을 측정하여 공중합체의 분자량과 구조가 용해도에 미치는 영향을 조사하였다. 초임계 분산중합에서의 효과적인 계면활성력을 확인하였고, 성장하는 입자의 안정화에 필요한 키 파라미터를 결정하기 위해 다양한 조건에서 실험을 수행하였으며, 화장품 분야에 응용될 수 있는 새로운 구조의 친환경 고분자 소재 개발에 이 연구가 작용될 수 있다는 잠재적인 가능성을 확인하였다.

• 폴리머
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• 제38권1호
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• pp.16-23
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• 2014

A novel poly(AM-DMDAAC)/MMT superabsorbent nanocomposites are prepared by radical polymerization using ammonium persulfate (APS) and anhydrous sodium sulfite as a free radical initiator and N,N-methylene bisacrylamide (MBA) as a crosslinker. In this paper, an optimization study on the synthesis of superabsorbent nanocomposites is carried out. Orthogonal array experiment indicates that the optimized conditions is acrylamide (AM) content 23 wt%, diallyl dimethyl ammonium chloride (DMDAAAC) content 6 wt%, montmorillonite (MMT) content 4 wt%, initiator content 0.2 wt% and crosslinker content 0.02 wt%. Under the optimization syntheses conditions concluded, the maximum water absorbency in distilled water is $659.53g{\cdot}g^{-1}$ and in 2 wt% sodium chloride solution is $116.25g{\cdot}g^{-1}$. Compared with the range values of different factors ($R_j$), the order of significance factors in distilled water is C (MMT) > B (DMDAAC) > A (AM) > D (crosslinker) > E (initiator). MMT is intercalated during polymerization reaction and a nanocomposite structure is formed as shown by TEM analysis and XRD analysis.