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211.
Keeyoon Sung 《Journal of Quantitative Spectroscopy & Radiative Transfer》2007,107(3):385-406
Ground-based solar absorption infrared spectra were recorded in the Canadian Arctic during the early spring of 2004 using a moderate-resolution Fourier transform spectrometer, the Portable Atmospheric Research Interferometric Spectrometer for the Infrared (PARIS-IR). As part of the Canadian Arctic Atmospheric Chemistry Experiment (ACE) validation campaign, the PARIS-IR instrument recorded solar absorption spectra of the atmosphere from February to March 2004 as the Sun returned to the Arctic Stratospheric Ozone Observatory (AStrO) near Eureka, Nunavut, Canada (80.05°N, 86.42°W). In this paper, we briefly outline the PARIS-IR instrument configuration and data acquisition in the high Arctic. We discuss the retrieval methodology, characterization and error analysis associated with total and partial column retrievals. We compare the PARIS-IR measurements of N2O and O3 column amounts with those from the Fourier transform spectrometer (ACE-FTS) onboard the Canadian SCISAT-1 satellite and the ozonesonde data obtained at Eureka during the validation campaign. 相似文献
212.
In this paper, we proposed a novel infrared absorbing structure for uncooled infrared detectors. The infrared absorber makes use of a quarter-wavelength structure composed of a dielectric layer, a protecting layer, an active layer, a supporting layer and a reflecting layer. Sputtered amorphous silicon is used as a dielectric layer because of its high refractive index. We fabricated the uncooled microbolometer with the proposed infrared absorbing structure by surface micromachining method. Then we characterized various bolometric properties such as thermal conductance, thermal time constant, responsivity and infrared absorptance. The fabricated bolometer showed the thermal conductance of 6.72 × 10−7 W/K, the thermal mass of 4.43 × 10−9 J/K, the thermal time constant of 6.6 ms and the responsivity of 7.76 × 103 V/W at 10 Hz chopper frequency and 9.22 μA bias current. From the results, the estimated absorptance is about 80%. We expect that the proposed absorbing structure shows high infrared absorption and high performance of uncooled microbolometer. 相似文献
213.
Hyun Sik Yoon Chung Ho Jeon Jae Hwan Jung Bonguk Koo Changyoung Choi Sung Chul Shin 《国际流体数值方法杂志》2013,73(3):250-265
In the present paper, a direct forcing/fictitious domain (DF/FD)–level set method is proposed to simulate the twophase flow–body interaction. The DF/FD does not sacrifice accuracy and robustness by employing a discrete δ (Dirac delta) function to transfer quantities between the Eulerian nodes and Lagrangian points explicitly as the immersed boundary method. The advantages of this approach are the simple concept, the easy implementation and the utilization of original governing equation without modification. The main idea is to combine DF/FD method with the level set method in the Cartesian coordinates. We present the results of a number of test cases to illustrate the effectiveness of the proposed method for single‐phase flow–body interaction problem and the two‐phase flows with a stationary body. Eventually, the simulations of various water entry problems have been conducted to validate the capability and the accuracy of the present method on solving the twophase flow–body interaction. Consequently, the present results are found to be in good agreement with those of previous studies. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
214.
An experimental and computational investigation into the autoignition of methanol under high‐pressure and low‐to‐intermediate temperature conditions is conducted. The ignition delay results have been obtained using a heated rapid compression machine, over a pressure range of 7–30 bar, a temperature range of 850–1100 K, and an equivalence ratio range of 0.25–2.0. Using kinetic schemes recently reported in the literature for the combustion of methanol, the experimental results are compared to computationally obtained values. The kinetic schemes studied are found to significantly underpredict ignition delays for the conditions investigated. A sensitivity analysis of the computed results to reaction rate constants is also conducted. It is shown that the reaction of methanol with HO2 radical is critical to the predicted values of ignition delays under the current experimental conditions. © 2011 Wiley Periodicals, Inc. Int J Chem Kinet 43: 175–184, 2011 相似文献
215.
Kyung Hwan Kim Dae Sung Chung Chan Eon Park Dong Hoon Choi 《Journal of polymer science. Part A, Polymer chemistry》2011,49(1):55-64
New dithienothiophene‐containing conjugated polymers, such as poly(2,6‐bis(2‐thiophenyl‐3‐dodecylthiophene‐2‐yl)dithieno[3,2‐b;2′,3′‐d]thiophene, 4 and poly(2,6‐bis (2‐thiophenyl‐4‐dodecylthiophene‐2‐yl)dithieno[3,2‐b;2′,3′‐d]thiophene, 8 have been successfully synthesized via Stille coupling reactions using dodecyl‐substituted thiophene‐based monomers, bistributyltin dithienothiophene, and bistributyltin bithiophene; these polymers have been fully characterized. The main difference between the two polymers is the substitution position of the dodecyl side chains in the repeating group. Grazing‐incidence X‐ray diffraction (GI‐XRD) gave clear evidence of edge‐on orientation of polycrystallites to the substrate. The semiconducting properties of the two polymers have been evaluated in organic thin film transistors (OTFTs). The two conjugated polymers 4 and 8 exhibit fairly high hole carrier mobilities as high as μave = 0.05 cm2/Vs (ION/OFF = 3.42 × 104) and μave = 0.01 cm2/Vs, (ION/OFF = 1.3 × 105), respectively, after thermal annealing process. The solvent annealed films underwent reorganization of the molecules to induce higher crystallinity. Well‐defined atomic force microscopy (AFM) topography supported a significant improvement in TFT device performance. The hole carrier mobilities of the solvent annealed films are comparable to those obtained for a thermally annealed sample, and were one‐order higher than those obtained with a pristine sample. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010 相似文献
216.
Jaehong Kim Sung Heum Park Jinwoo Kim Shinuk Cho Youngeup Jin Joo Young Shim Hyunmin Shin Sooncheol Kwon Il Kim Kwanghee Lee Alan J. Heeger Hongsuk Suh 《Journal of polymer science. Part A, Polymer chemistry》2011,49(2):369-380
Newly designed 2H‐benzimidazole derivatives which have solubility groups at 2‐position have been synthesized and incorporated into two highly soluble carbazole based alternating copolymers, poly[2,7‐(9‐(1′‐octylnonyl)‐9H‐carbazole)‐alt‐5,5‐(4′,7′‐di(thien‐2‐yl)‐2H‐benzimidazole‐2′‐spirocyclohexane)] (PCDTCHBI) and poly[2,7‐(9‐(1′‐octylnonyl)‐9H‐carbazole)‐alt‐5,5‐(4′,7′‐di(thien‐2‐yl)‐2H‐benzimidazole‐2′‐spiro‐4′′‐((2′′′‐ethylhexyl)oxy)‐cyclohexane)] (PCDTEHOCHBI) for photovoltaic application. These alternating copolymers show low‐band gap properties caused by internal charge transfer from an electron‐rich unit to an electron‐deficient moiety. HOMO and LUMO levels are –5.53 and –3.86 eV for PCDTCHBI, and –5.49 and –3.84 eV for PCDTEHOCHBI, respectively. Optical band gaps of PCDTCHBI and PCDTEHOCHBI are 1.67 and 1.65 eV, respectively. The new carbazole based the 2H‐benzimidazole polymers show 0.11–0.13 eV lower values of band gaps as compared to that of carbazole based benzothiadiazole polymer, poly[N‐9′‐heptadecanyl‐2,7‐carbazole‐alt‐5,5‐(4′,7′‐di‐2‐thienyl‐2′,1′,3′‐benzothiadiazole)] (PCDTBT), while keeping nearly the same deep HOMO levels. The power conversion efficiencies of PCDTCHBI and PCDTEHOCHBI blended with [6,6]phenyl‐C71‐butyric acid methyl ester (PC71BM) are 1.03 and 1.15%, respectively. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
217.
You Jin Cho Hyo Jin No Mi Sung Kim Ju‐Yeon Lee 《Journal of polymer science. Part A, Polymer chemistry》2011,49(8):1784-1790
Novel Y‐type polyester 4 containing 5‐methyl‐4‐{5‐(1,2,2‐tricyanovinyl)‐2‐thiazolylazo}resorcinoxy groups as nonlinear optical (NLO) chromophores, which are parts of the polymer backbone, was prepared, and its NLO properties were investigated. Polyester 4 is soluble in common organic solvents such as N,N‐dimethylformamide and dimethylsulfoxide. Polymer 4 shows a thermal stability up to 250 °C from thermogravimetric analysis with glass‐transition temperature obtained from differential scanning calorimetry of approximately 94 °C. The second harmonic generation (SHG) coefficient (d33) of poled polymer film at 1560‐nm fundamental wavelength is 8.12 × 10?9 esu. The dipole alignment exhibits a thermal stability even at 6 °C higher than glass‐transition temperature (Tg), and no significant SHG decay is observed below 100 °C due to the partial main‐chain character of polymer structure, which is acceptable for NLO device applications. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
218.
Polyethylene terephthalates (PETs) with well‐defined chemical structures were prepared by molecular design, and the effect of the chemical structure on the physical properties of PET was investigated. Hydroxyl‐group end‐capped PETs with ηinh = 0.4–0.6 dL/g exhibited a viscosity behavior similar to Bingham fluids, although other PETs with similar molecular weights (MWs) showed Newtonian flow behavior. This rheological feature was more noticeable for hydroxyl‐group end‐capped branched PETs. In addition, hydroxyl‐group end‐capped branched PETs became solidlike from 80 rad/s as the frequency was increased. On the other hand, hydroxyl end‐capped linear PETs showed a noticeable viscoelastic transition peak around 20 rad/s. High MW linear and branched PETs with ηinh ≥ 0.9 prepared by multistep synthesis showed non‐Newtonian fluid behavior. © 2001 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 39: 1027–1035, 2001 相似文献
219.
Alexander Ryabchun Alexey Bobrovsky Sung‐Ho Chun Valery Shibaev 《Journal of polymer science. Part A, Polymer chemistry》2013,51(19):4031-4041
A new approach to the synthesis of photoactive comb‐shaped homo‐ and copolyamides containing azobenzene, cinnamate, and coumarin side groups for photoalignment of liquid crystals was elaborated. Photooptical properties and photoorientational ability of these polymers with respect to liquid crystals were studied. It was shown that polarized UV irradiation of all spin‐coated polyamides leads to orientation of liquid crystalline molecules deposited on the polyamide thin films. The synthesized polymers containing cinnamate and coumarin side groups as well as azobenzene‐containing cyano‐ and nitro‐substituted polymers demonstrated good orientation ability in relation to liquid crystals displaying photoinduced planar orientation with high dichroism values within the range of 0.68–0.72. Contrary to the above‐mentioned polyamides, azobenzene‐containing fluorosubstituted polymers induced a homeotropic orientation of liquid crystals. It was shown that the synthesized photoactive polyamides can be considered as promising photoalignment materials for application in display technology, photonics, and other “smart” optical devices. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013 , 51, 4031–4041 相似文献
220.
Sung Joong Lee Semin Park Jin Young Choi Jae‐Han Shim Eun‐Ho Shin Jeong‐Heui Choi Soo Taek Kim A. M. Abd El‐Aty Jong Sung Jin Dong Won Bae Sung Chul Shin 《Biomedical chromatography : BMC》2009,23(7):719-731
It would be preferable for pesticide residues substituted by hydrolyzable functionality to be analyzed after cooking because their structures are apt to degrade during boiling and/or heating. A liquid chromatography–tandem mass spectrometry (LC‐MS/MS) method for the quantitative determination of 44 pesticide residues with hydrolyzable functional group in five typical vegetable widely consumed in Republic of Korea is described. The sample clean‐up was carried out according to the method of Food Code No. 83 established by the Korea Food and Drug Administration (KFDA). Zorbox XDB‐C18 column was selected for the analysis because of the best peak separation. The LC mobile phase consisted of water and 5 mm methanolic ammonium formate, which resulted in a peak shape with good symmetry at each run. Tandem mass spectroscopic (MS/MS) experiments were performed in ESI positive mode and the multiple reaction monitoring modes. A conventional matrix effect was modified to more comprehensive form 100γij (%). A high matrix effect (30%) was detected for the seven polar pesticides, namely thiamethoxam, clothianidin, acetamiprid, aldicarb, thiacloprid, pirimicarb and methabenzthiazuron. The limits of detection were in the range of 0.1–8.1 µg/kg, indicating a good sensitivity. Most of the recoveries ranged from 70 to 131% with RSDs ≤ 20%. The current method allowed rapid quantitation and identification of low pesticide levels in the cooked vegetable samples. Of the screened pesticide residues, only fluquinconazole and dimethomorph below the maximum residue levels established by the KFDA were detected in onion and cucumber samples. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献