• Journal of Food Hygiene and Safety
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• v.38 no.6
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• pp.517-527
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• 2023

This study aimed to examine the possibility of upcycling extracts of Angelica keiskei and Oenanthe javanica juice by-products through comparing enzyme extraction (EE) and complex extraction (CE) methods to increase the extraction yield and flavor of materials. A higher extraction yield was obtained for free amino acid content with EE and CE for A. keiskei and O. javanica juice by-products, respectively, and a higher extraction efficiency was achieved with juice by-products than with extracts prepared from raw materials before juice production. The content of major amino acids varied depending on the extraction method used. When used according to the characteristics of the extract, their use as a functional material was confirmed along with improvement in the flavor of the food. Consistently high extraction yields for organic acid and sugar levels were obtained with CE in A. keiskei and O. javanica juice by-products. The DPPH radical scavenging ability and TPC were consistently high with CE in A. keiskei and O. javanica juice by-products; the increase in extracted content was likely because of the reaction between the ethanol used for CE and the phenolic compounds. However, because the antioxidant capacity of the juice by-product extracts was somewhat lower than that of the extracts from raw materials before juice production, the amount used should be reviewed. The TFC was found to be higher in extracts obtained with EE than with CE for A. keiskei juice by-products; however, no significant difference was observed between EE and CE in the O. javanica juice by-products. Through this study, the taste compounds and antioxidant properties of extracts obtained from juice by-products produced after the production of A. keiskei and O. javanica green juice were analyzed, and the availability of high value-added materials was confirmed. Based on these research results, expanding specific R&D for practical use should be explored.

• Membrane Journal
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• v.23 no.4
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• pp.290-296
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• 2013

Poly(vinylidenefluoride-co-chlorotrifluoroethylene) P(VDF-co-CTFE) polymer was attached to methacrylic acid (MAA) in the presence of 1,8-diazabicyclo[5,4,0]undec-7-ene(DBU) catalyst to prepare P(VDF-co-CTFE)-MAA copolymer. The modified P(VDF-co-CTFE)-MAA was polymerized with 2-sulfoethyl methacrylate (SEMA) monomer in the presence of 4',4'-azobis(4-cyanovaleric acid(ACVA) initiator by free radical polymerization to form the proton conducting membrane. The ratio of the SEMA was increased in the membrane to increase the presence of the acidic group. The maximum IEC value that was observed at 50% SEMA was around 0.82 meq/g, which is consistent with the water uptake value. The highest proton conductivity achieved by P(VDF-co-CTFE)-MAA/SEMA membrane with 50% SEMA was approximately 0.041 S/cm. This indicates that the available ionic group for the proton conduction increases with the increase in the SEMA in the membrane.

• Applied Chemistry for Engineering
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• v.27 no.4
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• pp.433-438
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• 2016

The current study evaluated the air quality of the smoking booth equipped with the air purification system consisting of photocatalysts and air filters by measuring the concentrations of hazardous substances of tobacco smoke such as CO, HCHO, $CH_3CHO$, PM10 and PM2.5. To enhance the removal efficiency of hazardous substances, an infrared ray was exposed to improve the reactivity of OH radical generated from the photocatalyst toward environmental tobacco smoke (ETS) gas phase hazardous materials. It was found that the smoking booth with the air purification system improved the removal efficiency of hazardous substances containing formaldehyde by 85.2% compared to that of the smoking booth without any purification systems. In addition, the removal efficiency of the fine dust after treatment was enhanced up to 89.4%.

• Journal of Korea Soil Environment Society
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• v.5 no.3
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• pp.3-15
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• 2001

The ozone kinetics including ozone auto-decomposition. effect of pH, and solubility were investigated. Diesel decomposition process including TCE & PCE decomposition. effect of hydroxyl radical scavenger, effect of pH, and ozone/$H_2O$$_2$by ozonation process were also examined using deionized water, simulated groundwater. and actual groundwater. Reactions with deionized water and groundwater both stowed the second-order reaction rates, and the reaction rate was much higher in groundwater (half-life of 14.7 min) than in deionized water (hal(half-life of 37.5 min). The reaction rate was accelerated at high pH values in both waters. The use of ozone showed high oxidation rates of TCE. PCE and diesel. Though hydroxyl radical scavengers existing in groundwater were inhibitors for treating diesel, high pH condition and addition of hydrogen peroxide could accelerate to degrade diesel in groundwater, indicating ozone oxidation process could be applied to treating diesel contaminated-groundwater.

• Magazine of the Korea Concrete Institute
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• v.7 no.2
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• pp.175-182
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• 1995

Styrene-Maleic anhydride copolymer (SMA) was prepared by the radical copolmerization of styrene and maleic anhydride using ${\alpha}-{\alpha}'$ azobis(isobutyronitrile) as an initiatrr. SMA was further reacted with m-amino phenol to obtain aminophenol-substituted SMR (mSMA). Sulfonated SMA and mSMA were also prepared by the reaction of copolymers with sulfuric acid The copolyniers were characterized by infrared spectroscopy. It was found from the results of elemental analysis that the substitution degree of aminophenol in the mSMR is 44% and the degree is lowered to 35% after sulfonation. The percentage of copolymers adsorbed on the surface of cement particles was increased with a decrease of added copolymers. While, the arnourit of sulfonated SMA absorbed on the surface of cement particles was larger than that of the sulfonated mSMA The copolymers synthesized in this study are probably expected as a high range water reducer for coiicxte.

• Applied Chemistry for Engineering
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• v.20 no.4
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• pp.386-390
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• 2009

In this study, sulfadiazine acrylamide monomer was synthesized by the reaction of sulfadiazine, known as an antibiotic substance, with acryloyl chloride. The monomer was characterized by $^1H-NMR$, and $^{13}C-NMR$. Using the synthesized sulfadiazine acrylamide monomer and styrene monomer, a copolymer, poly(styrene-co-sulfadiazine), was obtained by the free radical copolymerization and characterized by $^1H-NMR$, GPC, DSC and TGA. The copolymer nanofibers web has been successfully prepared by electrospinning technique under DMF solution. The diameter of the nanofibers was in the range between 500 and 800 nm. Antibacterial activity of the nanofiber web was evaluated utilizing the colony counting method against Staphylococcus aureus and Escherichia coli.

• Polymer(Korea)
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• v.25 no.5
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• pp.736-743
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• 2001

An electro- active polymer (EAP) (poly(2-acrylamido-2- methyl propane sulfonic acid), PAMPS) gel crosslinked with N,N-methylenebisacrylamide (MBAA) has been prepared by free radical polymerization in aqueous solution with potassium persulfate as initiator PAMPS gel was swollen in surfactant solution to substitute surfactant for using as actuator. PAMPS gel showed a large movement in the surfactant solution by electric field. PAMPS gel showed the reversible binding and fast response rate. Bending mechanism of gel is related to the cooperative process of hydrophobic interaction, swelling-deswelling of gel and the electrostatic attraction between anode (+) and the anions of PAMPS gel. The response rate of PAMPS gel was increased as the applied potential and the degree of cross-linkage were increased. The response rate was increased as the bending cycle was repeated, but it was decreased with increasing the gel thickness.

• Journal of the Korean Ceramic Society
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• v.42 no.4
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• pp.237-244
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• 2005

We prepared the cylindrical $\gamma-alumina$ pellets of 5 mm in diameter and 10 mm in average length using amorphous alumina and pore generating agent. The pellets were immersed in an aqueous solution of the mixture of $Fe(NO_{3})_{3}{\cdot}9H_{2}O$ and $CH_{3}COOH$. They were then hydrothermally treated at $200^{\circ}C$ for 3 h in autoclave, dried and calcined. For the application as an environmental catalyst, we investigated the decomposition characteristics of aniline and the initiation characteristics of $OH^{\cdot}$ conversion action in $O_{3}$ environment with or without the $Fe_{2}O_{3}$ supported y-alumina catalyst and $O_{3}$ molecule.

• Proceedings of the Materials Research Society of Korea Conference
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• 2011.05a
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• pp.23.1-23.1
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• 2011

최근 화석연료를 대체하기 위한 지속가능한 신에너지에 대한 요구가 증대됨에 따라 태양광 발전에 대한 연구도 폭발적으로 늘어가고 있는 추세이다. 태양광이 화석연료 대체에너지로 실효성을 가지기 위해서는 태양광 발전 시스템의 발전효율을 높이고 생산 비용을 저감하는 문제가 선결되어야 한다. 기존 실리콘 태양전지 시스템 설비 비용의 60% 이상을 차지하는 모듈의 제조과정에서 소재 손실을 최소화함으로써 저가격화를 실현하고자 박막형 태양전기 기술이 태동되었다. 현재 박막 태양전지와 관련하여 활발한 기술 개발이 진행되고 있으며 상당한 시장 점유율을 보이고 있는 실정이다. 박막 태양전지 분야에서 CIGS와 같은 화합물 반도체 박막 태양전지 시장이 확대되고 있는 실정을 고려한다면 실리콘 박막 태양전지의 경우 고효율화 저가격화 달성은 더욱 절실한 문제이다. 실리콘 박막의 경우 독성이 없으며 고갈 우려가 없는 소재이면서 기존의 직접회로 산업의 인프라 구조를 활용할 수 있어 많은 기대와 관심을 끌고 있는 박막 태양전지 후보이다. 박막 태양전지 제조에 있어서 핵심기술은 도핑된 실리콘층과 광흡수를 위한 진성 실리콘층을 합성하는 공정 기술이다. 현재 박막 태양전지 산업에서 실리콘 박막 소재의 합성은 주로 PECVD법에 의해 이루어지고 있다. 그러나 스퍼터 공정을 이용한 실리콘 박막 합성 연구 또한 20년 이상의 오랜 기간 동안 연구되어 오고 있다. 스퍼터 공정을 이용한 실리콘 박막합성는 독성 가스를 사용하지 않으며, 디스플레이와 같은 기존의 소자 공정 기술을 채용할 수 있다는 장점을 가지고 있어 주목 받고 있다. 실제로 반응성 마그네트론 스퍼터링에 의해 제조된 실리콘 박막은 PECVD공정에 의한 실리콘 박막에 상응하는 우수한 광전자적 특성을 보인다. 스퍼터 공정에서는 박막 성장을 위한 수송 물질들이 열적 평형 상태에 근접한 라디칼들이라기 보다 대부분 고에너지 원자종과 이온들이 주류를 이루고 있어 합성된 실리콘 박막의 결함 제어가 어렵다는 문제가 있다. 박막 합성 기구의 규명을 통하여 이러한 문제를 해결하기 위한 시도들이 이루어 지고 있으며, 본 발표를 통하여 스퍼터 공정을 이용한 태양전지용 실리콘 박막 합성기술에 대한 현황을 소개하고자 한다.

• Polymer(Korea)
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• v.34 no.1
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• pp.79-83
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• 2010

Alginate beads were prepared using poly(N-isopropylacrylamide-co-dimethylamino ethyl methacrylate)(P(NIPAM-co-DMAEMA)). First, P(NIPAM-co-DMAEMA) was immobilized on the surface of alginate beads by taking advantage of electrostatic interaction between alginate and P(NIPAM-co-DMAEMA). Second, P(NIPAM-co-DMAEMA) was contained in the matrix of alginate beads. P(NIPAM-co-DMAEMA) were prepared by a free radical polymerization at $74^{\circ}C$ for 12 h. The weight ratio of NIPAM to DMAEMA monomer was 95/5. The copolymer was identified by $^1H$-NMR. Releases from the alginate beads were observed at 30, 37, and $45^{\circ}C$ using blue dextran or FITC-dextran(fluorescein isothiocyanate-dextran) as a model drug. The effect of temperature on the degree of release from the beads was insignificant. FITC-dextran was released more than blue dextran possibly due to its smaller molecular weight.