• 제목/요약/키워드: Reaction Products

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촉매를 이용한 폐고분자 물질의 자원화 II. 연질 폴리우레탄 폼의 글리콜분해반응 메카니즘 (Catalytic Recycling of Waste Polymer II. A Study of the Mechanism on the Catalytic Glycolysis of Flexible Polyurethane Foam)

  • 박종래;김성익;김영철;박남국;서곤
    • 공업화학
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    • 제10권3호
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    • pp.388-393
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    • 1999
  • 폴리우레탄 폼은 반복된 우레탄과 우레아 그룹을 가지고 있는 고분자 물질이다. 연질 폴리우레탄 폼을 이루고 있는 이 두 그룹들은 반응온도 $200^{\circ}C$, 글리콜, 초산 칼륨 촉매 존재 하에서 가열시키면 에스테르교환반응에 의해 분해되어 액상의 생성물을 형성한다. GPC, IR 분석을 이용한 생성물의 분자량과 성분 함량분포 측정을 통하여 촉매글리콜분해 반응기구를 조사하였다. 폴리우레탄 폼의 에스테르교환 반응에서는 우레탄 그룹이 우레아 그룹의 분해 반응속도보다 빨랐다. 이온화 경향이 큰 potassium acetate 촉매를 사용함으로써 alkoxide의 친핵성이 증진되어 에스테르교환 반응속도를 촉진시킴을 알 수 있다. 또한, potassium acetate와 strontium acetate 촉매를 사용한 촉매글리콜분해반응은 서로 같은 반응경로로 반응이 진행되지만 반응속도의 차이로 생성물을 구성하는 성분의 함량이 다름을 알 수 있었다.

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폐오일을 이용한 아마이드계 아스팔트 박리방지제의 합성 및 특성 분석 (The Synthesis and characterization of of asphalt anti-stripping agents, amides synthesized from waste oils)

  • 이상아;김지웅;조남준
    • 분석과학
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    • 제29권6호
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    • pp.300-304
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    • 2016
  • 폐지방산과 ethylenediamine 또는 N,N'-bis (2-hydroxyethyl)ethylenediamine으로부터 아스팔트 박리방지제를 합성하였다. FT-IR과 NMR을 이용하여 분석한 결과 아마이드결합의 생성 및 박리방지제의 합성이 성공적으로 수행되었음이 확인하였다. 합성된 여러 종류의 박리방지제의 접착특성은 접촉각과 BBS 시험을 통해 비교하였다. 접촉각 측정으로부터 에틸렌다이아민과 동물유지로부터 제조된 시료가 가장 소수성이 컸으며, BBS 시험으로부터 수분저항성도 94%로 가장 우수한 것으로 나타났다. 그러나 에틸렌다이아민과 폐식용유의 반응생성물이 수분처리 전과 후의 절대적인 접착력은 각각 약 3610 및 3227 kPa로 가장 우수하였다. 전반적으로 접착력은 ED의 반응생성물이 HEED의 반응생성물보다 우수하였으며, 폐식용유나 동물유지의 반응생성물들이 순수한 콩기름의 반응생성물들보다 우수하였다.

Amino-carbonyl 반응에 의한 glucose-poly-${\gamma}$-glutamate (Glu-PGA) 갈변 반응물질의 항산화적 특성 연구 (Antioxidative Characteristics of Browning Reaction Products of Glucose-Poly-${\gamma}$-Glutamate (GIu-PGA) obtained from Amino-carbonyl Reaction)

  • 이남근;함영태
    • 한국식품과학회지
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    • 제37권5호
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    • pp.812-815
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    • 2005
  • 청국장 점질물인 PGA의 갈변 및 갈변 반응물질의 분획에 따른 갈변도와 전자 공여능에 따른 항산화력을 알아보았다. PGA의 갈변은 자체적으로는 갈변이 잘 일어나지 않고, 염기적 조건 하에서 glucose을 첨가하고 가열하면 갈변이 급격하게 일어나며 전자 공여능 또한 높게 나타났다. 염기적 조건 하에서 얻은 PGA 갈변 반응 물질(Glu-PGA, pH 8.2)을 Sephadex G-50을 이용하여 분획하고, 분획에 따른 갈변도 및 DPPH를 이용한 전자 공여능을 측정하였다. 분획된 갈변 반응 물질들은 비교적 광범위한 갈변도 및 전자 공여능을 보여 주었다. 이들 중 갈변도 및 전자 공여능이 상대적으로 높은 F-7과 F-20의 UV-VIS 흡수대에 있어서는 F-20은 멜라노이딘의 흡수대인 260-320nm에 걸쳐 완만한 흡수곡선을 나타내었고, F-7은 270nm 부근에서 특징적인 최대 흡수대를 나타내었다. 두 분획 물질의 분자량은 SDS-PAGE로 분석한 결과 F-7은 대략 35kDa 이상으로 나타났고, F-20은 SDS-PAGE상에서 뚜렷한 크기는 알 수 없었으나, F-7 보다는 비교적 저분자량을 갖는 물질이라는 것을 알 수 있었다.

고온 자전 연소합성법과 기계적 미분에 의한 준나노 크기의 Ba-Zn Ferrite 분말의 제조 (Preparation of Quasi-nano-sized of Ba-Zn Ferrites Powders by Self-Propagating High Temperature Synthesis and Mechanical Milling)

  • 최경숙;이종재;김혁돈;최용;이상헌
    • 전기학회논문지
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    • 제57권4호
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    • pp.625-628
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    • 2008
  • Ba-Zn ferrite powders for electromagnetic insulator were synthesized by self-propagating high-temperature synthesis(SHS) with a reaction of $xBaO_2+(1-x)ZnO+0.5Fe_2O_3+Fe{\rightarrow}Ba_xZn_{1-x}Fe_2O_4$. In this study, phase indentification of SHS products was carried out by using x-ray diffractometry and quasi-nano sized Ba-Zn powders were prepared by a pulverizing process. SHS mechanism was studied by thermodynamical analysis about oxidation reaction among $BaO_2,\;ZnO,\;Fe_2O_3$, and Fe. As oxygen pressure increases from 0.25 MPa to 1.0 MPa, the SHS reactions occur well and make clearly the SHS products. X-ray analysis shows that final SHS products formed with the ratio of $BaO_2/ZnO$ of 0.25, 1.0 and 4.0, are mainly $Ba_xZn_{1-x}Fe_2O_4$. Based on thermodynamical evaluation, the heat of formation increases in the order of $ZnFe_2O_4,\;BaFe_2O_4$, and $Ba_xZn_{1-x}Fe_2O_4$. This supports that $Ba_xZn_{1-x}Fe_2O_4$ phase is predominately formed during SHS reaction. The SHS reactions to form $Ba_xZn_{1-x}Fe_2O_4$ depends on oxygen partial pressure, and the heat of formation during the SHS reaction. The SHS reactions tends to occur well with increasing the oxygen partial pressure and BaO2/ZnO ratio in the reactants This means that the SHS reaction for the formation of Ba-Zn ferrite includes the reduction of BaO2/ZnO and the oxidation of Fe. $Ba_xZn_{1-x}Fe_2O_4$ powders after pulverizing is agglomeratedwith a size of about $50{\mu}m$, in which quasi-nano sized particles with about 300nm are present.

Simultaneous Analysis of Cholesterol Oxidation Products (COPs) in Powdered Milk Using HPLC/UV-Vis

  • Lee, Jin Joo;Myung, Seung-Woon
    • Bulletin of the Korean Chemical Society
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    • 제34권9호
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    • pp.2787-2794
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    • 2013
  • Cholesterol and cholesterol oxidation products (COPs) may accumulate in foods of animal origin during processing or storage. An effective and sensitive analytical method was developed by increasing the UV absorption of compounds through derivatization by attaching a chromophore to the functional groups of cholesterols (cholesterol, 20-hydroxycholesterol, 7-ketocholesterol, cholestane-$3{\beta}$-$5{\alpha}$-$6{\beta}$-triol, 25-hydroxycholesterol, and $5,6{\alpha}$-epoxycholesterol). The influences of the reaction time, volume of reaction solvent, amounts of derivatizing reagent, and extraction solvents were investigated, as they may influence the reaction and extraction yield. The derivatized COPs were analyzed simultaneously on a C18 column (2.1 mm i.d. ${\times}$ 100 mm length, $3.5{\mu}m$ particle size) using a gradient elution with water and acetonitrile. The derivatized COPs showed increased sensitivity and selectivity in HPLC/UV-Vis. The LOD and LOQ were in the concentration ranges of 0.018-0.55 mg/kg and 0.059-1.84 mg/kg from the powdered milk. And the accuracy and precision were 78.1-116.7% and 1.1-9.9%, respectively.

저농도 은이 함유된 LTCC 전극공정부산물로부터 은 회수 및 나노입자 제조 연구 (Study on the Recovery Silver and Nanoparticles Synthesis from LTCC By-products of Lowly Concentrated Silver)

  • 주소영;안낙균;이찬기;윤진호
    • 한국분말재료학회지
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    • 제25권3호
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    • pp.232-239
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    • 2018
  • In this paper, the recovery and nanoparticle synthesis of Ag from low temperature co-fired ceramic (LTCC) by-products are studied. The effect of reaction behavior on Ag leaching conditions from the LTCC by-products is confirmed. The optimum leaching conditions are determined to be: 5 M $HNO_3$, a reaction temperature of $75^{\circ}C$, and a pulp density of 50 g/L at 60 min. For the selective recovery of Ag, the [Cl]/[Ag] equivalence ratio experiment is performed using added HCl; most of the Ag (more than 99%) is recovered. The XRD and MP-AES results confirm that the powder is AgCl and that impurities are at less than 1%. Ag nanoparticles are synthesized using a chemical reduction process for recycling, $NaBH_4$ and PVP are used as reducing agents and dispersion stabilizers. UV-vis and FE-SEM results show that AgCl powder is precipitated and that Ag nanoparticles are synthesized. Ag nanoparticles of 100% Ag are obtained under the chemical reaction conditions.

Use of Hydrazine for Pitting Corrosion Inhibition of Copper Sprinkler Tubes: Reaction of Hydrazine with Corrosion By-Products

  • Suh, Sang Hee;Kim, Sohee;Suh, Youngjoon
    • Corrosion Science and Technology
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    • 제16권5호
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    • pp.247-256
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    • 2017
  • The feasibility of using hydrazine for inhibiting pitting corrosion in copper sprinkler tubes was investigated by examining microscopical and structural evolution of corrosion by-products with SEM, EDS, and XRD. Hydrazine removed dissolved oxygen and reduced CuO and $Cu_2O$ as well. The stable phase was changed from CuO to $Cu_2O$ or Cu depending on hydrazine concentration. Hydrazine concentration of 500 ppm could convert all CuO corrosion by-products to $Cu_2O$. In a tightly sealed acryl tube filled with aqueous solution of 500 ppm hydrazine, octahedral $Cu_2O$ particles were formed while plate-like structures with high concentration of Cu, O, N and C were formed near a corrosion pit. The inside structure of a corrosion pit was not altered by hydrazine aqueous solution. Uniform corrosion of copper was almost completely stopped in aqueous solution of 500 ppm hydrazine. Corrosion potential of a copper plate was linearly dependent on log (hydrazine concentration). The concept of stopping pitting corrosion reaction by suppressing oxygen reduction reaction could be verified by applying this method to a reasonable number of real sprinkler systems before full-scale application.

Trichoderma koningii에서 분비되는 .$\beta$-D-glucosidase의 반응산물에 대한 핵자기공명분석 ($^{1}$H-NMR spectroscopic evidence on the glycosidic linkages of the transglycosylated products of low-molecular-weight $\beta$-D-glucosidase from trichoderma koningii)

  • 이헌주;정춘수;강사욱;하영칠
    • 미생물학회지
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    • 제27권1호
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    • pp.35-42
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    • 1989
  • The mode of transglycosylation reaction observed during the action of low-molecular-weigh $\beta$-D-glucosidase ($\beta$-D-glucoside glucohydrolase, EC3.2.1.21) purified from Trichoderma koningii ATCC 26113 was investigated using $^{1}H$-NMR spectroscopy. The enzyme was purified by the series of procedures including ammonium sulfate precipitation, and fractionations by column chromatographies on Bio-Gel P-150, DEAE-Sephadex A-50, and SP-Sephadex C-50. The final purification was performed by the band eluation after preparative polyacrylamide gel electrophoresis. The enzyme showed its molecular size of 78,000 through the analysis of sodium dodecyl sulfate-polyacrylamide gel electrophoresis and its isoelectric point of 5.80 through the analysis of analytical isoelectric focusing. The H-1 proton resonances were analyzed. After the reaction of the enzyme with cellobiose, the reaction products were separated by high performance liquid chromatography using refractive index detector. H-1 resonances of the products were consisted with those of gentiobiose [$\beta$-D-glucopyranosyl--(1,6)-D-glucopyranose], and cellotriose [$\beta$-D glucopyranosyl-(1,4)-$\beta$-D-glucopyranosyl]-(1,4)-D-glucopyranose] with minor resonances of sophorose [$\beta$-D-glucopyranosyl-(1,2)-D-glucopyranose], respectively.

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Photo-DSC를 사용한 에틸렌글리콜 단위 길이에 따른 다이메타크릴레이트의 광중합 전환률에 미치는 온도와 광개시제 농도의 영향 (The Effect of Temperature and Photoinitiator Concentration on Conversion of Photopolymerized Multiethylene Glycol Dimethacrylate by Photo-DSC)

  • 도현성;김대준;김현중;이영규
    • 접착 및 계면
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    • 제4권3호
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    • pp.14-20
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    • 2003
  • UV 경화에 사용되는 poly(ethylene glycol 400) dimethacrylate(PEGA400DMA)와 ethylene glycol dimethacrylate(EGDMA)를 사용하여 모노머(monomer)의 종류에 따른 경화거동과 광개시제의 양과 온도에 따른 경화 거동을 photo-DSC를 사용하여 살펴보았다. Ethylene glycol의 단위길이가 늘어날수록, 광개시제의 양이 증가할수록, 반응 온도가 높을수록 경화속도가 빠르게 일어났다. 또한 PEG400DMA의 반응속도가 EGDMA보다 느리게 나타났지만 전환률은 높게 나타남을 알 수 있었다.

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Study on Maillard Reaction Products Derived from Aqueous and Ethanolic Fructose-Glycine and Its Oligomer Solutions

  • Kim, Ji-Sang
    • Preventive Nutrition and Food Science
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    • 제15권4호
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    • pp.297-303
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    • 2010
  • The present study compared the Maillard reaction products (MRPs) derived from aqueous and ethanolic fructoseglycine and its oligomer (dimer and trimer) solutions. The pH was lower in glycine (G) than in diglycine (DG) and triglycine (TG) in both aqueous and ethanolic solutions, but the pH difference between the DG and TG was not significant. MRPs derived from the DG had a greater absorbance at 294 and 420 nm in ethanolic solution than in an aqueous solution. In particular, the loss of sugar was higher in ethanolic solution than in aqueous solution. Enolization of fructose was observed in both aqueous and ethanolic MRP solutions; however, enolization was not observed for the G in aqueous MRP solutions. The glycine oligomer content in ethanolic MRP solutions remained higher than that in aqueous MRP solutions. Furthermore, neither diglycine nor triglycine were detected in the G aqueous or ethanolic MRP solutions, while triglycine was detected in both the DG aqueous and ethanolic MRP solutions. Absorption in the ultraviolet-visible (UV-Vis) spectra was higher with MRPs derived from the ethanolic solution than with those derived from the aqueous solution. MRPs derived from the DG in an ethanolic solution showed the highest absorption intensity.