• Title/Summary/Keyword: reaction time

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Sequential use of real-time polymerase chain reaction and enzyme-linked immunosorbent assay techniques verifies adulteration of fermented sausages with chicken meat

  • Benli, Hakan;Barutcu, Elif
    • Animal Bioscience
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    • 제34권12호
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    • pp.1995-2002
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    • 2021
  • Objective: Detection of adulteration in processed meats is an important issue for some countries due to substitution of beef with a cheaper source of protein like poultry. In this study, the presence of chicken meat was investigated using real-time polymerase chain reaction (real-time PCR) and enzyme-linked immunosorbent assay (ELISA) techniques to verify adulteration of fermented sausage samples. Methods: A total of 60 commercial samples were collected from 20 establishments in three replicates including 10 fermented sausage manufacturers and 10 butchers to investigate the presence of chicken meat with the sequential use of real-time PCR and ELISA techniques. In addition, pH, moisture content, water activity and color values of the samples were determined. Results: Both real-time PCR and ELISA showed agreement on the presence or absence of chicken meat in 55 out of 60 fermented sausage samples and chicken meat was identified with both methods in 16 samples. Five samples produced inconsistent results for the presence of chicken meat in the first run. Nevertheless, the presence of chicken meat was verified with both methods when these samples were analyzed for the second time. In addition, the average physico-chemical values of the fermented sausage samples tested positive for chicken meat were not significantly different from some of those fermented sausage samples tested negative for the chicken meat. Conclusion: The sequential use of real-time PCR and ELISA techniques in fermented sausages could be beneficial for the government testing programs to eliminate false negatives for detection of adulteration with chicken meat. Furthermore, consumers should not rely on some of the quality cues including color to predict the adulteration of fermented sausages with chicken meat since there were no statistical differences among some of the samples tested positive and negative for chicken meat.

페놀 수지의 경화 공정 (Curing Process of Phenolic Resin)

  • 이윤배;성시창;신은정
    • 공업화학
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    • 제16권2호
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    • pp.292-295
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    • 2005
  • 자동차 브레이크 패드 만들 때 페놀 수지의 경화 시간은 원가 질감의 중요한 요인이 된다. 이 경화 시간은 페놀수지와 경화제인 Hexamethylenetetramine의 반응 시간을 측정함으로써 알 수 있다. 이 반응 시간은 적외선 분광법(FT-IR), 열치사 주사법(DSC) 및 열중량 분석법(TGA)에 의하여 화학 반응의 완결을 추적하여 알아낼 수 있었다.

Modeling reaction injection molding process of phenol-formaldehyde resin filled with wood dust

  • Lee, Jae-Wook;Kwon, Young-Don;Leonov, A.I.
    • Korea-Australia Rheology Journal
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    • 제20권2호
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    • pp.59-63
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    • 2008
  • A theoretical model was developed to describe the flow behavior of a filled polymer in the packing stage of reaction injection molding and predict the residual stress distribution of thin injection-molded parts. The model predictions were compared with experiments performed for phenol-formaldehyde resin filled with wood dust and cured by urotropine. The packing stage of reaction injection molding process presents a typical example of complex non-isothermal flow combined with chemical reaction. It is shown that the time evolution of pressure distribution along the mold cavity that determines the residual stress in the final product can be described by a single 1D partial differential equation (PDE) if the rheological behavior of reacting liquid is simplistically described by the power-law approach with some approximations made for describing cure reaction and non-isothermality. In the formulation, the dimensionless time variable is defined in such a way that it includes all necessary information on the cure reaction history. Employing the routine separation of variables made possible to obtain the analytical solution for the nonlinear PDE under specific initial condition. It is shown that direct numerical solution of the PDE exactly coincides with the analytical solution. With the use of the power-law approximation that describes highly shear thinning behavior, the theoretical calculations significantly deviate from the experimental data. Bearing in mind that in the packing stage the flow is extremely slow, we employed in our theory the Newtonian law for flow of reacting liquid and described well enough the experimental data on evolution of pressure.

Manufacturing of Copper(II) Oxide Powder for Electroplating from NaClO3 Type Etching Wastes

  • Hong, In Kwon;Lee, Seung Bum;Kim, Sunhoe
    • Journal of Electrochemical Science and Technology
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    • 제11권1호
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    • pp.60-67
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    • 2020
  • In this study, copper (II) oxide powder for electroplating was prepared by recovering CuCl2 from NaClO3 type etching wastes via recovered non-sintering two step chemical reaction. In case of alkali copper carbonate [mCuCo3·nCu(OH)2], first reaction product, CuCo3 is produced more than Cu(OH)2 when the reaction molar ratio of sodium carbonate is low, since m is larger than n. As the reaction molar ratio of sodium carbonate increased, m is larger than n and Cu(OH)2 was produced more than CuCO3. In the case of m has same values as n, the optimum reaction mole ratio was 1.44 at the reaction temperature of 80℃ based on the theoretical copper content of 57.5 wt. %. The optimum amount of sodium hydroxide was 120 g at 80℃ for production of copper (II) oxide prepared by using basic copper carbonate product of first reaction. At this time, the yield of copper (II) oxide was 96.6 wt.%. Also, the chloride ion concentration was 9.7 mg/L. The properties of produced copper (II) oxide such as mean particle size, dissolution time for sulfuric acid, and repose angle were 19.5 mm, 64 second, and 34.8°, respectively. As a result of the hole filling test, it was found that the copper oxide (II) prepared with 120 g of sodium hydroxide, the optimum amount of basic hydroxide for copper carbonate, has a hole filling of 11.0 mm, which satisfies the general hole filling management range of 15 mm or less.

Influence of Reaction Conditions on the Grafting Pattern of 3-Glycidoxypropyl trimethoxysilane on Montmorillonite

  • He, Wentao;Yao, Yong;He, Min;Kai, Zhang;Long, Lijuan;Zhang, Minmin;Qin, Shuhao;Yu, Jie
    • Bulletin of the Korean Chemical Society
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    • 제34권1호
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    • pp.112-116
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    • 2013
  • Surface modification of montmorillonite (MMT) with 3-glycidoxypropyl trimethoxysilane (3GTO) in mild methanol/water mixture has been investigated in detail. The influence of reaction conditions (including silane concentration in feed, reaction time and reaction temperature) on the grafting amount and yield of silane, and further on the grafting pattern of silanes was studied by thermogravimetric analysis, elemental analysis, X-ray diffraction (XRD) and BET. Higher silane concentration, longer reaction time and higher reaction temperature are all benefit to higher grafting amount. When the grafting reaction was performed with 3 mmol/g silane concentration, at $90^{\circ}C$ for 24 h, the grafted amount and yield of silane reached 1.4443 mmol/g and 30%, respectively. Based on the XRD and BET data analysis, a speculation that the grafting pattern of silanes was concentration dependence was proposed.

카올리나이트 KGa-1b (표준 점토)의 인산염 탈착 특성 (Phosphate Desorption of Kaolinite KGa-1b (Source Clay))

  • 조현구;김순오;추창오;도진영
    • 한국광물학회지
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    • 제22권4호
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    • pp.289-295
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    • 2009
  • 카올리나이트 KGa-1b (표준 점토)의 인산염 탈착 특성을 규명하기 위하여 벳치(batch) 흡착-탈착 실험을 실시하였으며, 탈착 과정은 연속추출법에 따라 pH 4에서 시행하였다. 인의 함량은 UV 분광분석기를 시용하여 측정하였으며, 이 때 파장은 820 nm를 이용하였다. 카올리나이트의 인산염 흡착-탈착 반응은 비가역적으로 일어나며, 흡착된 대부분의 인산염은 고착되는 경향을 나타낸다. 인산염 탈착 등온선은 반응 시간이 짧은 경우 프로인드리히 등온선에, 반응 시간이 긴 경우 탬킨 등온선에 더 일치하는 경향을 보인다. 인산염 탈착 반응은 초기의 빠른 반응과, 후기의 느린 반응으로 구분된다. 흡착된 인산염의 농도가 높아질수록 탈착률은 감소하는 경향을 보이며, 탈착 시간이 길어지면 탈착률은 감소하는 경향을 보여준다.

실리카 나노입자 표면에 결합된 아미노기와 Glycidyl Methacrylate의 반응에 관한 분광학적 연구 (Spectroscopic Studies on the Reaction between Amino Groups on Silica Nanoparticle Surface and Glycidyl Methacrylate)

  • 이상미;하기룡
    • 폴리머
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    • 제37권6호
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    • pp.777-783
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    • 2013
  • 본 연구에서는 실리카 나노입자를 dipodal 형태의 bis[3-(trimethoxysilyl)propyl]amine(BTMA) 실란 커플링제로 실리카 표면을 개질한 후, glycidyl methacrylate(GMA)로 표면 처리를 하여 실리카에 결합된 BTMA의 N-H기와 GMA의 epoxide기의 개환 반응에 의하여 실리카 표면에 중합용 methacrylate기를 도입하는 연구를 수행하였다. 반응시간, 반응온도 및 투입하는 GMA의 농도 변화가 BTMA의 N-H기와 GMA의 epoxide기 사이의 반응에 미치는 영향을 Fourier transform infrared spectroscopy(FTIR), elemental analysis(EA) 및 고체상태 $^{13}C$ cross-polarization magic angle spinning(CP/MAS), nuclear magnetic resonance spectroscopy(NMR)법을 사용하여 분석하였다. BTMA로 개질된 실리카를 GMA로 처리하면 실리카 입자에 결합되어 있는 BTMA의 N-H기와 GMA의 epoxide기가 열리면서 상호 반응이 일어났으며, 실험한 조건에서는 반응시간, 반응온도 및 투입하는 GMA 농도가 증가할수록 실리카 표면에 도입되는 methacrylate기가 증가함을 확인하였다.

편마암-물 반응계에서 지하수의 지화학적 진화 및 이차광물 생성에 관한 반응경로 모델링 (Reaction Path Modelling on Geochemical Evolution of Groundwater and Formation of Secondary Minerals in Water-Gneiss Reaction System)

  • 정찬호;김천수;김통권;김수진
    • 한국광물학회지
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    • 제10권1호
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    • pp.33-44
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    • 1997
  • The reaction path of water-gneiss in 200m borehole at the Soorichi site of Yugu Myeon, Chungnam was simulated by the EQ3NR/EQ6 program. Mineral composition of borehole core and fracture-filling minerals, and chemical composition of groundwater was published by authors. In this study, chemical evolution of groundwater and formation of secondary minerals in water-gneiss system was modelled on the basis of published results. The surface water was used as a starting solution for reaction. Input parameters for modelling such as mineral assemblage and their volume percent, chemical composition of mineral phases, water/rock ratio reactive surface area, dissolution rates of mineral phases were determined by experimental measurement and model fit. EQ6 modelling of the reaction path in water-gneiss system has been carried out by a flow-centered flow through open system which can be considered as a suitable option for fracture flow of groundwater. The modelling results show that reaction time of 133 years is required to reach equilibrium state in water-gneiss system, and evolution of present groundwater will continue to pH 9.45 and higher na ion concentration. The secondary minerals formed from equeous phase are kaolinite, smectite, saponite, muscovite, mesolite, celadonite, microcline and calcite with uincreasing time. Modeling results are comparatively well fitted to pH and chemical composition of borehole groudwater, secondary minerals identified and tritium age of groundwater. The EQ6 modelling results are dependent on reliability of input parameters: water-rock ratio, effective reaction surface area and dissolution rates of mineral phases, which are difficult parameters to be measured.

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Zn bath 프로세스에 의한 폐초경합금의 재활용에 관한 기초연구(I) (A Basic Study on the Recycling of Wasted Cemented Carbide by the Zn Bath Process(I))

  • 김경식;김인호;이찬기;송창빈
    • 자원리싸이클링
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    • 제29권6호
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    • pp.35-40
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    • 2020
  • 본 연구에서는 zinc bath 프로세스에 의한 폐초경합금의 재활용 시 중요한 반응온도, 시간 및 아연의 첨가량 등 반응 메카니즘을 조사하기 위해 기초실험을 수행하였다. 그 결과, zinc bath 반응은 용융 아연(Zn)과 폐초경합금 내측의 코발트(Co)의 반응을 촉진시키기 위해 800℃ 이상에서 가열하는 것이 요구되었다. 또한 폐초경합금의 두께는 800℃에서 0.5~2시간 동안의 zinc bath 프로세스에 있어서 반응시간의 증가에 따라 선형적으로 감소하였으며, 아연의 증발 감소량을 줄이기 위해서는 800℃이하에서 3시간 가열된 후에 2.0×10 torr-2이상의 진공분위기로 900℃이상에서 1시간 동안 가열하는 것이 적합한 것으로 조사되었다.

고질소 둔감에너지 물질인 DNAM(Dinitroammeline) 합성공정 개발 (Synthesis of a Nitrogen-rich Insensitive Energetic Material, DNAM(Dinitroammeline))

  • 설민정;김민준;김진석;김승희
    • 한국추진공학회지
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    • 제20권1호
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    • pp.50-57
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    • 2016
  • 본 논문은 DNAM(Dinitroammeline)합성공정 개발을 위한 Lab scale 합성 과정을 소개하고 분석결과를 기록한 것으로 주요 내용은 다음과 같다 Melamine을 출발물질로 하여 니트로화와 산화 반응을 통해 DNAM을 합성하였다. 수율과 순도의 최적 조건을 찾기 위해 투입순서, 반응시간, 반응물 당량 등을 변경하여 실험을 수행하였다. DNAM 합성의 최적화된 조건은 3시간에서 3시간 30분 정도 반응시간이고, 니트로화 혼합물의 무게비는 1:1.4(아세트산 무수물:농질산)이며, 최종 수율은 60% 이상이다.