• 제목/요약/키워드: linear dynamic range

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용융중합에 의한 분지형 폴리카보네이트의 유변학적 특성 연구 (A Study on the Rheological Properties of Branched Polycarbonates by Melt Polymerization)

  • 최수정;윤경화;김희승;유승윤;김연철
    • 폴리머
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    • 제35권4호
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    • pp.356-362
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    • 2011
  • 폴리카보네이트(polycarbonate, PC)에 화학적 구조가 다른 두 가지의 분지제를 첨가하여 용융중합으로 분지형 폴리카보네이트(branched PC, B-PC)를 합성하였다. 분지제의 함량은 0.001~0.005 mol% 내에서 조절하였다. 합성된 PC의 화학구조는 FTIR, $^1H$ NMR파 $^{13}C$ NMR 스펙트럼을 이용하여 확인하였으며, 분자량, 유리전이온도 및 분해온도는 GPC, DSC와 TGA를 이용하여 측정하였다. Phloro type의 분지제를 가지는 B-PC의 분자량에 낮은 값을 보여주었으며, 유리전이온도는 분자량에 따라 증가하였다. 두 형태의 B-PC 모두 선형 PC와 비교하였을 때 낮은 주파수(frequency) 영역에서 복합점도(complex viscosity)가 높게 나타났고, shear thinning 현상이 크게 나타났다. Shear thinning의 정도를 표시하는 power law index(n)는 선형회귀분석에 의해 계산되었고 0.483~0.996 범위의 값을 보여주었다. Phloro 타입의 B-PC가 높은 shear thinning 경향을 보였으며 이들 B-PC의 유변학적 특성은 동적유변측정기를 이용하여 측정하였다.

Novel Triiodide PVC-Based Membrane Sensor Based on a Charge Transfer Complex of Iodine and Bis(2-hydroxyacetophenone)butane-2,3-dihydrazone

  • Ganjali, Mohammad Reza;Norouzi, Parviz;Shirvani Arani, Simindokht;Salavati Niasari, Masoud
    • Bulletin of the Korean Chemical Society
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    • 제26권11호
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    • pp.1738-1742
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    • 2005
  • In this study a novel triiodide ion-selective electrode based on a charge transfer complex of iodine and Bis(2-hydroxyacetophenone)butane-2,3-dihydrazone (ICT), as a membrane carrier was prepared. The electrode has a linear dynamic range between 1.0 ${\times}$ $10^{-2}$ and 5.0 ${\times}$ $10^{-7}$ M, with a Nernstian slope of 58. 99 ${\pm}$ 0.3 mV $decade^{-1}$ and detection limit of 3.0 ${\times}$ $10 ^{-7}$ M. The potentiometric response of the proposed sensor is independent of the pH of the solution in the pH range of 3.0-10.0. The electrode possesses the advantages of short conditioning time, fast response time, and especially, very good selectivity over a large number of common organic and inorganic anions. The electrode can be used for at least 6 months without any considerable divergences in the potentials. It was used as an indicator electrode in potentiometric titration of triiodide ion with thiosulfate.

Membrane Inlet-based Portable Time-of-flight Mass Spectrometer for Analysis of Air Samples

  • Kim, Tae-Kyu;Jung, Kyung-Hoon;Yoo, Seung-Kyo;Jung, Kwang-Woo
    • Bulletin of the Korean Chemical Society
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    • 제26권2호
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    • pp.303-308
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    • 2005
  • A miniaturized time-of-flight mass spectrometer with an electron impact ionization source and sheet membrane introduction has been developed. The advantages and features of this mass spectrometer include high sensitivity, simple structure, low cost, compact volume with field portability, and ease of operation. A mass resolution of 400 at m/z 78 has been obtained with a 25 cm flight path length. Under optimized conditions, the detection limits for the volatile organic compounds (VOCs) studied were 0.2-10 ppm by volume with linear dynamic ranges greater than three orders of magnitude. The response times for various VOCs using a silicone membrane of 127 $\mu$m thickness were in the range 4.5-20 s, which provides a sample analysis time of less than 1 minute. These results indicate that the membrane introduction/time-of-flight mass spectrometer will be useful for a wide range of field applications, particularly for environmental monitoring.

비선형을 고려한 파랑중 선체 운동과 강도 응답에 관한 연구 (A Study on the Response of the Motions and Strength of Ships in Waves taking account of Non-linerities)

  • 김창렬;김진안;김사수;홍봉기;배동명
    • 대한조선학회지
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    • 제24권1호
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    • pp.51-66
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    • 1987
  • In this paper, the authors investigate theoretically the motion and longitudinal strength of ships among waves talking account of the effects of nonlinearities such as the hull shape, bottom emergence, and hydrodynamic impact. Incidentally the ship is treated as an elastic beam in heading wave condition regarding characteristics of slamming and whipping-according to the variation in the range of a quarter length of the ship forward and the increase of the elastic modes up to 4-th vibration mode were investigated by the present theory. Calculations are performed for 97m container ship and its validity is confirmed by a series of model tests. Conclusions obtained are as follows; 1) Acceleration and pressure estimated by the present theory are in good accordance with experiments. 2) The present non-linear theory may be applied for estimating longitudinal bending moment of ships in slamming and whipping conditions. 3) In investigation of the characteristic in response according to shape variation for parts under draft and vow-flare in the range of a quarter length of the ship forward, dynamic responses due to the former were much more conspicuous than those due to the later. 4) In the maximum bending moment, the considering case up to 2-the mode are larger, about $10{\sim}15%$, than that up to 4-th mode.

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Anodic Stripping Differential Pulse Voltammetric Determination of Trace Amounts of Lead after Preconcentration of Its Complex with 2-(5-Bromo-2-pyridylazo)-5-diethylaminophenol onto Natural Analcime Zeolite by Column Method

  • Taher, Mohammad Ali;Mostafavi, Ali;Afzali, Darush;Rezaeipour, Ebrahim
    • Bulletin of the Korean Chemical Society
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    • 제25권8호
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    • pp.1125-1129
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    • 2004
  • This work assesses the potential of natural Analcime Zeolite as an adsorbent for preconcentration of lead (II) traces. Lead is quantitatively retained on 2-(5-bromo-2-pyridylazo)-5-diethylaminophenol by column method with Analcime in the pH range of 5-6.5 and 2 mL $min^{?1}$ flow rate. Lead was removed from the column with 10.0 mL of 4 M hydrochloric acid and was determined by anodic stripping differential pulse voltammetry. 0.5ppb detection limit was obtained and linear dynamic range was 3 to $1.2{\times}10^5$ ppb in final solution with correlation coefficient of 0.999 and relative standard deviation of ${\pm}$ 1.2% (for eight replicate determination of 2.5 ${\mu}g\;mL^{?1}$ of lead). Various parameters such as the effect of pH, flow rate, instrumental conditions and interferences of some ions on the determination of lead have been studied in detail for optimization of conditions. The method was successfully applied for determination of lead in various samples.

Sensors Comparison for Observation of floating structure's movement

  • Trieu, Hang Thi;Han, Dong Yeob
    • 한국항해항만학회:학술대회논문집
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    • 한국항해항만학회 2014년도 추계학술대회
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    • pp.219-221
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    • 2014
  • The objective of this paper is to simulate the dynamic behavior of a floating structure model, using image processing and close-range photogrammetry, instead of the contact sensors. Previously, the movement of structure was presented through the exterior orientation estimation of a single camera by space resection. The inverse resection yields the 6 orientation parameters of the floating structure, with respect to the camera coordinate system. The single camera solution is of interest in applications characterized by restriction in term of costs, unfavorable observation conditions, or synchronization demands when using multiple cameras. This article discusses the theoretical determinations of camera exterior orientation based on Direct Linear Transformation and photogrammetric resection using least squares adjustment. The proposed method was used to monitor the motion of a floating model. The results of six degrees of freedom (6-DOF) by inverse resection show that the appropriate initial values by DLT can be effectually applied in least squares adjustment, to obtain the precision of exterior orientation parameters. Additionally, a comparison between the close-range photogrammetry and total station results was feasibly verified. Therefore, the proposed method can be considered as an efficient solution to simulating the movement of floating structure.

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Lead(II)-selective Polymeric Electrode Using a Schiff Base Complex of N,N'-Bis-thiophene-2-ylmethylene-ethane-1,2-diamine as an Ion Carrier

  • Jeong, Tae-Jun;Jeong, Dae-Cheol;Lee, Hyo-Kyoung;Jeon, Seung-Won
    • Bulletin of the Korean Chemical Society
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    • 제26권8호
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    • pp.1219-1224
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    • 2005
  • We prepared lead ion-selective PVC membranes that were based on N,N'-bis-thiophene-2-ylmethylene-ethane-1,2-diamine as a membrane carrier. The membrane electrode has a linear dynamic range between 1.0 ${\times}$ $10^{-5}$ and 1.0 ${\times}$ $10^{-1}$ M with a Nernstian slope of 29.79 mV per decade, and its detection limit was 2.04 ${\times}$ $10^{-6}$ M at room temperature. The potentiometric response is independent of the pH of the solution in the pH range of 5-7. The proposed electrode revealed good selectivity and response for $Pb^{2+}$ over a wide variety of other metal ions in pH 5.0 buffer solutions, and there was good reproducibility of the base line on the subsequent measurements. The membrane electrode has a relatively fast response time, satisfactory reproducibility and a relatively long life time.

Determination of Ultra Trace Levels of Copper in Whole Blood by Adsorptive Stripping Voltammetry

  • Attar, Tarik;Harek, Yahia;Larabi, Lahcen
    • 대한화학회지
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    • 제57권5호
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    • pp.568-573
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    • 2013
  • A selective and sensitive method for simultaneous determination of copper in blood by adsorptive differential pulse cathodic stripping voltammetry is presented. The procedure involves an adsorptive accumulation of Cu(II)-ETSC (4- ethyl-3-thiosemicarbazide) on a hanging mercury drop electrode, followed by a stripping voltammetry measurement of reduction current of adsorbed complex at about -715 mV. The optimum conditions for the analysis of copper (II) ion are : pH 10.3, concentration of 4-ethyl-3-thiosemicarbazide $3.25{\times}10^{-6}$ M and an accumulation potential of -100 mV. The peak current is proportional to the concentration of copper over the range 0.003-125 ng/mL with a detection limit of 0.001 ng/mL and an accumulation time of 60 s. Moreover, with the use of the proposed method, there is a considerable improvement in the detection limit, the linear dynamic range and the deposition time, compared with the methods of adsorptive stripping voltammetry for the determination of copper. The developed method was validated by analysis of whole blood certified reference materials.

Novel Thallium(I)-Selective Membrane Electrode Based on a Podal Ligand

  • Ganjali, Mohammad Reza;Pourjavid, Mohammad Reza;Mouradzadegun, Arash;Hosseini, Morteza;Mizani, Farhang
    • Bulletin of the Korean Chemical Society
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    • 제24권11호
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    • pp.1585-1589
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    • 2003
  • A PVC-based membrane electrode for thallium(I) ions based on 1,21,23,25-tetramethyl-2,20: 3,19-dimetheno-[H, 2] H, 23H, 25H-bis-[1,3] dioxocino[5,4-i:5',4'-i] benzo [1,2-d: 5.4-d'] bis [1,3] benzodioxocin(II) has been prepared. The electrode displays a linear dynamic range of $1.0{\times}10^{-1}-1.0{\times}10^{-5}$ M, with a Nernstian slope of $59.8{\pm}0.2\;mV\;{decad^-1}$, and a detection limit $5.0{\times}10^{-6}$ M. It has a very fast response time of<10 s and can be used for at least ten weeks without a considerable divergence in potentials. This electrode revealed comparatively good selectivity with respect to alkali, alkaline earth, and some transition and heavy metal ions and was effective in a pH range of 2.0-10.0. It was used as an indicator electrode in potentiometric titration of thallium ion with sulfide ion.

Studies on the Spectrophotometric Determination and Electrochemical Behavior of Heavy Lanthanide Ions in Nonaqueous System and Heavy Metal Chelate Complexes with Bidentate Legands: (Part I) Flow Injection Spectrophotometric Determination of Heavy Lanthanide Ions with Xylenol Orange

  • Sam-Woo Kang;Chong-Min Park;Kwang-Hee Cho;Hong-Seock Han
    • Bulletin of the Korean Chemical Society
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    • 제14권1호
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    • pp.59-62
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    • 1993
  • Spectrophotometric determination of some heavy lanthanide ions by flow injection method is described. Xylenol Orange forms water soluble chelates with lanthanide ions in a tris[hydroxymethyl]-aminomethane-buffered medium having pH 8.3 and containing cetyltrimethylammonium bromide. The molar absorptivities of Ln(III)-XO complexes were increased by the ternary system with cetyltrimethylammonium bromide with the concomitant bathochromic shift of absorption maxium compared to those of the binary system without cetyltrimethylammonium bromide. The calibration curves are linear in the range 0.25-1.00 ppm for Gd(III), Dy(III), Er(III), Tm(III) and Yb(III) and the dynamic range are very wide. The detection limits (S/N=2) are from 2 ppb for Gd(III) to 30 ppb for Yb(III) and the relative standard deviations are from 1.2% for 0.5 ppm Gd(III) to 1.8% for 0.5 ppm Yb(III). The sample throughput was ca. 50 $h^{-1}$.