• 대한화학회지
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• 제21권1호
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• pp.60-66
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• 1977

m-Phenylenediamine(以下 MPD로 略함)과 resorcinol(以下 RES로 略함)을 몰比를 달리하면서 포름알데히드와 酸化觸媒 존재하에서 反應시켜 生成되는 附加共縮合型 樹脂를 流動파라핀을 사용하여 서스펜젼重合시켜 60∼80 mesh의 粒狀重合體를 合成하고 이를 精製한후 5, 10, 15, 20, $25{\%}$의 水酸化 나트륨 水溶液으로 처리한후, 原樹脂와 이들 알칼리 處理樹脂의 金屬이온들에 대한 吸着性을 檢討하였다. $Cd^{2+}$이온에 대한 흡착성은 原樹脂보다 水酸化나트륨水溶液을 처리한 경우 현저히 吸着性은 向上되지만 MPD : RES의 몰比 가 增加함에 따라 原樹脂의 경우와는 달리 減少하는 경향을 나타내며 $Pb^{2+}와\;Al^{3+}$이온들은 알칼리처리로 吸着能增加와 더불어 MPD : RES의 몰比가 2 : 1에서 最大値를 나타내며 $Ca^{2+}$이온의 경우는 MPD : RES의 몰比가 1 : 1에서 최대치를 나타내고 있다. $Mg^{2+}과\;Co^{2+}$이온들은 거의 類似한 傾向을 나타내어 MPD : RES의 몰比增加와 더불어 吸着能은 減少하는 傾向을 나타낸다. $Hg^{2+}$이온의 경우는 特異하며 MPD : RES의 몰比가 減少함에 따라 吸着能은 현저히 增加하는 경향을 나타내어 窒素含宥킬레이트와의 結合性이 强한 一般性과 잘 一致하고 있다. 이 系의 樹脂들은 輕金屬 이온(例 $Ca^{2+},\;Mg^{2+}$) 들보다 重金屬이온(例 $Cd^{2+},\;Hg^{2+}$)들에 對한 吸着力이 현저히 優秀하다.

• 한국어병학회지
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• 제26권3호
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• pp.265-274
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• 2013

동해안의 3개 정점(삼척, 영덕, 포항)과 서해안의 2개 정점(학암포, 만리포)에서 여름철(7, 8월)에 진두발을 채집하여 생장, 성숙, 배우체와 사분포자체 비율 및 질병에 대한 연구를 실시하였다. 진두발의 체장은 개체군별로 평균 6.10~9.69 cm였으며 만리포에서 최소였고 포항에서 최대로서 동해안 개체가 서해안 개체에 비해 큰 것으로 확인되었다. 개체가 서해안 진두발에 비해 큰 것을 확인하였다. 진두발 개체군의 영양체 비율은 26.7~66.7 %였으며, 영양체를 resorcinol 방법으로 구분한 후 배우체:사분포자체 비율은 동해안에서 1.7:1로 배우체가 우점하였고 서해안에서는 학암포에서 1:1.1, 만리포에서 1:2.3로서 포자체가 번무하였다. 본 연구에서 한국산 진두발은 다양한 질병(백색증과 녹반증 등), 내생조류와 착생조류를 가지고 있었으며, 여름철의 진두발은 건강한 조체는 20~40 %로서 많은 개체가 질병을 가지고 있었다. 진두발은 현재까지 동정되지 않은 사상형 녹조류인 내생하는 Ulvella sp.를 가지고 있었다. 이러한 내생조류는 유럽과 캐나다의 주름진두발에서 관찰되는 감염성 병원체로서 보다 많은 관심과 연구가 요구된다.

• Journal of the Korean Wood Science and Technology
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• 제46권3호
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• pp.213-220
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• 2018

리기다소나무를 구조용 집성재의 재료로 이용하기 위해 판면의 옹이와 대패가공 후 방치시간에 따른 수지 삼출량이 레조르시놀수지로 접착한 판재의 접착성능에 미치는 영향을 검토하였다. 고온($120{\sim}95^{\circ}C$) 및 저온($65{\sim}50^{\circ}C$)에서 건조한 리기다소나무의 수지 삼출량은 판목면이 정목면 보다 저온건조재가 고온건조재보다 많았다. 방치시간별로는 저온건조재는 3일째 고온건조재는 7일째에 최고함량을 보였고, 이후부터는 서서히 감소하여 15~90일에는 거의 차이가 없었다. 접착성능은 수지의 삼출이 많은 2~3일까지는 낮았으나 15일 이후에는 큰 차이가 없었으며, 고온 및 저온 건조재 모두 방치시간에 관계없이 KS 기준의 접착성능을 만족하였다. 옹이부가 포함된 적층 구성에서의 접착강도는 KS의 접착강도 기준 이상이었으나 목파율은 기준인 65% 이상을 만족하지 못하였다. 적층 단면구성(정목+정목, 판목+판목, 정목+판목)에 따른 접착성능은 고온 및 저온건조재 모두 모든 적층구성에서 KS의 기준을 크게 상회하였다.

• Elastomers and Composites
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• 제29권5호
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• pp.444-452
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• 1994

Emulsion graft copolymerizations of vinyl monomers, butyl acrylate(BA), methyl methacrylate(MMA), 2-ethylhexyl acrylate (EHA), glycidyl methacrylate (GMA), 2-hydroxyethyl methacrylate(HEMA), methacrylonitrile(MAN), dimethylaminoethyl methacrylate(DAMA) or 2-vinyl pyridine(VP), onto carboxyl-terminated SBR latex were carried out under different experimental conditions. In case of synthesizing SBR-g-poly(butyl acrylate), the degree of grafting was increased with increasing the amount of emulsifier, polymerization temperature and the amount of initiator. Pull-out strength of resorcinol-formaldehyde-latex(RFL) adhesives formulated with modified latexes was very higher than that of RFL adhesive formulated with ungrafted latex. When the modified latexes with GMA, HEMA, MAN, DAMA or VP were used, the break occurred at cords. Peel strength of RFL adhesives formulated with SBR-g-poly(GMA), SBR-g-poly(HEMA) or SBR-g-poly(VP) was higher by about 1.3 times than that of RFL adhesives formulated with unmodified SBR against nylon cord and was higher by about 2.0 times against polyester cord.

• Bulletin of the Korean Chemical Society
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• 제34권6호
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• pp.1755-1762
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• 2013

A graphene-Zn/Al layered double hydroxide composite film was simultaneously prepared by electrochemical deposition on the surface of a glassy carbon electrode (G-LDH/GCE) from the mixture solution containing GO and nitrate salts of $Zn^{2+}$ and $Al^{3+}$. The modified electrode showed good electrochemical performances toward the simultaneous electrochemical detection of hydroquinone (HQ), catechol (CA) and resorcinol (RE) due to the unique properties of graphene (G) and LDH such as large active surface area, facile electronic transport and high electrocatalytic activity. The redox characteristics of G-LDH/GCE were investigated with cyclic voltammetry and differential pulse voltammetry. The well-separated oxidation peak potentials, corresponding to the oxidation of HQ, CA and RE, were observed at 0.126 V, 0.228 V and 0.620 V respectively. The amperometric response of the modified electrode exhibited that HQ can be detected without interference of CA and RE. Under the optimized conditions, the oxidation peak current of HQ is linear with the concentration of HQ from 6.0 ${\mu}M$ to 325.0 ${\mu}M$ with the detection limit of 0.077 ${\mu}M$ (S/N=3). The modified electrode was successfully applied to the direct determination of HQ in a local tap water, showing reliable recovery data.

• 한국재료학회지
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• 제26권12호
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• pp.696-703
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• 2016

In this study, we intensively investigated the effect of conductive additive amount on electrochemical performance of organic supercapacitors. For this purpose, we assembled coin-type organic supercapacitor cells with a variation of conductive additive(carbon black) amount; carbon aerogel and polyvinylidene fluoride were employed as active material and binder, respectively. Carbon aerogel, which is a highly mesoporous and ultralight material, was prepared via pyrolysis of resorcinol-formaldehyde gels synthesized from polycondensation of two starting materials using sodium carbonate as the base catalyst. Successful formation of carbon aerogel was well confirmed by Fourier-transform infrared spectroscopy and $N_2$ adsorption-desorption analysis. Electrochemical performances of the assembled organic supercapacitor cells were evaluated by cyclic voltammetry, galvanostatic charge/discharge, and electrochemical impedance spectroscopy measurements. Amount of conductive additive was found to strongly affect the charge transfer resistance of the supercapacitor electrodes, leading to a different optimal amount of conductive additive in organic supercapacitor electrodes depending on the applied charge-discharge rate. A high-rate charge-discharge process required a relatively high amount of conductive additive. Through this work, we came to conclude that determining the optimal amount of conductive additive in developing an efficient organic supercapacitor should include a significant consideration of supercapacitor end use, especially the rate employed for the charge-discharge process.

• Macromolecular Research
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• 제15권4호
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• pp.324-329
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• 2007

An octa-functional alkoxyamine initiator, with the 2,2,6,6-tetramethyl-l-piperidinyloxy (TEMPO) free radical, was synthesized based on resorcinarene, with its efficiency to initiate the nitroxide-mediated free radical copolymerization of styrene and methyl methacrylate (MMA) described. A difunctional analogue of this initiator was also synthesized, using resorcinol as the core molecule. The structures of the resulting initiators were confirmed by homolysis studies based on electron spin resonance spectroscopy and molecular modeling. The polymerization behavior and characteristics of the polymers obtained using these two initiators were also compared. Well-defined star-shaped and linear random copolymers, with low polydispersities and controlled molecular weights, were prepared. The efficiencies of these initiators towards copolymerization, as well as the parameters permitting the formation of well-defined polymers, were also investigated. The reactivity ratios were $r_a=0.42(a=styrene)\;and\;r_b=0.33(b=MMA)$ for the octa-functional initiator system and $r_a=0.45\;and\;r_b=0.39$ for the difunctional initiator system.

• 동아시아식생활학회지
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• 제6권2호
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• pp.277-284
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• 1996

마(산마, 재배마)의 생리활성 물질의 기능성을 밝힐 목적으로 마의 갈변물질, 점질물 및 식이섬유를 분리 정제하여 항변이원성을 검색하여 다음과 같은 결과를 얻었다. 1. 마의 갈변효소를 cathol, hydroquinion, resorcinol, pyrogallol 등에 반응시켜 얻은 갈변물질의 항변이원성은 sodium azide에 대하여 기질에 따른 차이가 없었으나, 2-aminofloureno에 대해서는 모든 기질에서 유의적으로 높았다. (P＜0.01) 2. 마의 점질물과 식이섬유($\alpha$-cellulose, hemicellulose, pectin) 의 sodium azide와 2-ami-noflourene에 대한 항변이원성은 $\alpha$-cellulose와 hemicellulose에서 유의적으로 높았으며(p＜0.01), $\alpha$-cellulose와 흡착 반응시킨 2-amino-flourene에 대한 항변이원성은 5시간 반응시 가장 높았고 반응시간이 경과함에 따라 감소하였다.

• 한국응용과학기술학회지
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• 제14권1호
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• pp.109-115
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• 1997

Fluorescent anionic oligo surfactants were synthesized by the condensing products of long chain alkylvinylether-maleic anhydride cooligomers and resorcinol including dye structures. Their various surface activities and dispersing action were studied on the aqueous solution. These oligo surfactants exhibited a remarkable surface tension lowering property, lower foaming and a large dispersing action for the particles of ${\alpha}-copper$ phthalocyanine blue. Further it was ascertained that the binding of oligo surfactant onto the pigment surface caused the deviation towards lower wavelengths at the maximum fluorescent intensity as compared with aqueous oligo surfactant solutions, These surface active properties of the oligo surfactants may be attributed to rigid and hydrophobic structure of dye groups, besides surface-active groups of alkylether groups and carboxylic group of the anionic oligo surfactants.

• 한국염색가공학회지
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• 제11권4호
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• pp.50-56
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• 1999

The adhesive properties of polyester cord in rubber matrix were investigated according to the surface modification. The polyester cord was oxidized in sodium hypochlorite solution, and graft-polymerized with acrylic acid under the irradiation with ultraviolet light, and then coated with resorcinol-formaldehyde latex (RFL). The modified surface was checked with scanning electron microscope. The adhesive properties were measured by the full-Out method, and evaluated with regard to the energy of adhesion and the maximum load. The polyester was not oxidized in sodium hypochlorite solution, so the surface was not able to etch to produce the coarse topology. As the concentration of acrylic acid and the reaction time were increased, the graft yields were also increased. It was considered that the acrylic acid would swell the polyester and diffuse easily to the inner side of substrate. The adhesive properties of polyeser to rubber matrix were affected by the surface condition. Namely, the maximum load was almost same, but the energy of adhesion was rather higher In the polyester grafted with acrylic acid than in control one. We concluded that the flexible aliphatic chains of polyacrylic acid situated in the interface of cord and rubber matrix were distributed well the stress and strain all over the filler resulting the high energy of adhesion.