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排序方式: 共有575条查询结果,搜索用时 15 毫秒
61.
We report methods for preparation and tomographic reconstruction of an arbitrary single-photon path qubit. The arbitrary single-photon path qubit is prepared losslessly by passing the heralded single-photon state from spontaneous parametric down-conversion through variable beam splitter. Quantum state tomography of the single-photon path qubit is implemented by introducing path-projection measurements based on the first-order single-photon quantum interference. Using the state preparation and path-projection measurements methods for the single-photon path qubit, we demonstrate preparation and complete tomographic reconstruction of the single-photon path qubit with arbitrary purity. 相似文献
62.
Chang Dae Han Jinhwan Kim Deog Man Baek Sung Gun Chu 《Journal of Polymer Science.Polymer Physics》1990,28(3):315-341
The viscoelastic behavior, order-disorder transition, and phase equilibria in mixtures of a block copolymer and an endblock-associating resin were investigated. The block copolymer was a polystyrene-block-polyisoprene-block-polystyrene (KRATON® D-1107, Shell Development Co.) copolymer. The endblock-associating resins investigated were two different grades of a commercially available random copolymer of poly(α-methyl styrene) and polystyrene, one with a weight-average molecular weight \[\bar M_{\rm w}\] of 710 (KRISTALEX® 3085, Hercules Inc.) and the other with \[\bar M_{\rm w}\] = 4100 (KRISTALEX® 5140, Hercules Inc.). Mixtures of various proportions of the block copolymer and the endblock-associating resin were prepared in toluene solvent. With the mixtures, measurements of dynamic viscoelastic properties were made, namely, dynamic storage modulus G″ and dynamic loss modulus G″ as a function of temperature from temperature scans of the samples using a Rheometrics Mechanical Spectrometer. The following observations were made. (1) The plateau modulus of the block copolymer increased with increasing amount of KRISTALEX 3085 or KRISTALEX 5140, indicating that the low-molecular-weight resin was associated with the polystyrene microdomains of the block copolymer. (2) When KRISTALEX 3085 (up to 30 wt %) was added to the block copolymer, the glass transition temperature (Tg) of the polyisoprene midblock of the SIS block copolymer was shifted toward higher temperatures, indicating that part of the KRISTALEX 3085 added had associated with the rubbery midblock of the block copolymer. Also investigated was the order-disorder transition behavior of the mixtures, using a rheological technique (log G′ versus log G″ plots) recently introduced by Han and Kim. It has been found that the order-disorder transition temperature Tr of mixtures of the SIS block copolymer and KRISTALEX 3085 decreased steadily with increasing amount of KRISTALEX 3085, whereas the addition of KRISTALEX 5140 increased the Tr of the block copolymer. It was found by light scattering and hot-stage microscopy that macrophase separation occurred in the KRATON 1107/KRISTALEX 5140 mixtures while microdomains of polystyrene were present in the block copolymer. 相似文献
63.
Jong‐Beom Baek Frank W. Harris 《Journal of polymer science. Part A, Polymer chemistry》2005,43(24):6465-6479
A series of extended 6‐substituted quinoxaline AB monomer mixtures, 2‐(4‐fluorophenyl)‐3‐[4‐(4‐hydroxyphenoxy)phenyl]‐6‐substituted quinoxaline and 3‐(4‐fluorophenyl)‐2‐[4‐(4‐hydroxyphenoxy)phenyl]‐6‐substituted quinoxaline, were prepared and polymerized to afford phenylquinoxaline oligomers. High‐molecular‐weight polymers could not be obtained because of the formation of cyclic oligomers. On the basis of matrix‐assisted laser desorption/ionization time‐of‐flight analysis and molecular modeling results, the formation of a cyclic dimer could be a favorable process resulting in low‐molecular‐weight oligomers. They were completely soluble and amorphous, with glass‐transition temperatures varying from 165 to 266 °C, and they had thermooxidative stability, with samples displaying 5% weight loss temperatures of 419–511 °C in nitrogen. The thermal properties of the monomers and resultant polymers dramatically depended on the polarity of the substituents. The monomers and resultant oligomers displayed high fluorescence in tetrahydrofuran solutions and N‐methyl‐2‐pyrrolidinone solutions, respectively. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 6465–6479, 2005 相似文献
64.
Jong‐Beom Baek Frank W. Harris 《Journal of polymer science. Part A, Polymer chemistry》2004,42(24):6318-6330
A phenylquinoxaline (PQ) AB monomer mixture was treated with monofunctional and difunctional end‐capping agents and with and without a coupling agent to afford phenylethynyl‐terminated linear PQ oligomers. The resulting PQ oligomers were soluble in common organic solvents and had intrinsic viscosities (IVs) of 0.21–0.30 dL/g. The glass‐transition temperature (Tg) of the diphenylethynyl‐end‐capped PQ oligomer on both sides increased the most, from 215 °C (before curing) to 251 °C (after curing). The PQ AB2 monomer, which acted as both a coupling agent and a monomer for the hyperbranched polymer, was treated with an AB monomer and end‐capping agents to afford phenylethynyl‐terminated hyperbranched polyphenylquinoxalines (PPQs). They were also soluble in common organic solvents, had IVs of 1.00–1.65 dL/g and Tg's of 251–253 °C, and underwent exothermic cure with maxima around 412–442 °C. The Tg's of the cured hyperbranched PPQs ranged from 258 to 261 °C, depending on the number of phenylethynyl groups on the surface. After further curing, they displayed a Tg of 316 °C in one sample and turned into a fully crosslinked network. The dynamic melt viscosities of a linear oligomer (IV = 0.21 dL/g), a hyperbranched sample (IV = 1.00 dL/g), and a linear reference PPQ (IV = 1.29 dL/g) were compared with respect to the processing temperature. The PQ oligomer and hyperbranched PPQ had low melt viscosities. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 6318–6330, 2004 相似文献
65.
Indranil Roy Dinesh Shetty Raghunandan Hota Kangkyun Baek Jeesu Kim Chulhong Kim Sandro Kappert Kimoon Kim 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2015,127(50):15367-15370
Developing a material that can combat antibiotic‐resistant bacteria, a major global health threat, is an urgent requirement. To tackle this challenge, we synthesized a multifunctional subphthalocyanine (SubPc) polymer nanosphere that has the ability to target, label, and photoinactivate antibiotic‐resistant bacteria in a single treatment with more than 99 % efficiency, even with a dose as low as 4.2 J cm−2 and a loading concentration of 10 nM . The positively charged nanosphere shell composed of covalently linked SubPc units can increase the local concentration of photosensitizers at therapeutic sites. The nanosphere shows superior performance compared to corresponding monomers presumably because of their enhanced water dispersibility, higher efficiency of singlet‐oxygen generation, and phototoxicity. In addition, this material is useful in fluorescence labeling of living cells and shows promise in photoacoustic imaging of bacteria in vivo. 相似文献
66.
Jin Jeong Chang Nyung Kim Baek Youn Young Saeng Kim 《International Journal of Heat and Fluid Flow》2004,25(6):1006-1014
The thermal contact resistance is a principal parameter interfering with heat transfer in a fin–tube heat exchanger. However, the thermal contact resistance in the interface between tubes and fins has not been clearly investigated. The objective of the present study is to examine the thermal contact conductance for various fin–tube heat exchangers with tube diameter of 9.52 mm and to find a correlation between the thermal contact conductance and effective factors such as expansion ratio, fin type, fin spacing and hydrophilic coating. In this study, experiments have been conducted only to measure heat transfer rate between hot and cold water. To minimize heat loss to the ambient air by the natural convection fin–tube heat exchangers have been placed in an insulated vacuum chamber. Also, a numerical scheme has been employed to calculate the thermal contact conductance with the experimental data. As a result, a new correlation including the influences of expansion ratio, slit of fin and fin coating has been introduced, and the portion of each thermal resistance has been estimated in the fin–tube heat exchangers with 9.52 mm tube. 相似文献
67.
68.
Two cellular embeddings i: G → S and j: G → S of a connected graph G into a closed orientable surface S are equivalent if there is an orientation-preserving surface homeomorphism h: S → S such that hi = j. The genus polynomial of a graph G is defined by
$
g\left[ G \right](x) = \sum\limits_{g = 0}^\infty {a_g x^g ,}
$
g\left[ G \right](x) = \sum\limits_{g = 0}^\infty {a_g x^g ,}
相似文献
69.
Yong Hwan Lim Bum Ho Choi Young Baek Kim Dong Chan Shin 《Applied Surface Science》2010,256(23):6997-7000
We investigated the effects of in situ plasma-treatment on optical and electrical properties of index-matched indium tin oxide (IMITO) thin film. To render the IMITO-coated surface hydrophilic and study the optical and electrical characteristics, we performed in situ oxygen plasma post-treatment without breaking vacuum. The 94.6% transmittance in the visible wavelength range (400-700 nm) increased on average to 96.4% and the maximum transmittance reached 98% over a broad wavelength range. The surface roughness and sheet resistance improved from 0.9 nm and 200 Ω/sq to 0.0905 nm and 100 Ω/sq, respectively, by in situ plasma post-treatment. We confirmed by contact angle measurement that the hydrophobic IMITO surface was altered to hydrophilic. The improved optical and electrical characteristics of in situ plasma-treated IMITO makes it adequate for high-resolution liquid crystal on silicon displays. 相似文献
70.
The potential ability of atomic force microscopy (AFM) as a quantitative bioanalysis tool is demonstrated by using gold nanoparticles
as a size enhancer in a DNA hybridization reaction. Two sets of probe DNA were functionalized on gold nanoparticles and sandwich
hybridization occurred between two probe DNAs and target DNA, resulting in aggregation of the nanoparticles. At high concentrations
of target DNA in the range from 100 nM to 10 μM, the aggregation of gold nanoparticles was determined by monitoring the color
change with UV-vis spectroscopy. The absorption spectra broadened after the exposure of DNA–gold nanoparticles to target DNA
and a new absorption band at wavelengths >600 nm was observed. However, no differences were observed in the absorption spectra
of the gold nanoparticles at low concentrations of target DNA (10 pM to 10 nM) due to insufficient aggregation. AFM was used
as a biosensing tool over this range of target DNA concentrations in order to monitor the aggregation of gold nanoparticles
and to quantify the concentration of target DNA. Based on the AFM images, we successfully evaluated particle number and size
at low concentrations of target DNA. The calibration curve obtained when mean particle aggregate diameter was plotted against
concentration of target DNA showed good linearity over the range 10 pM to 10 nM, the working range for quantitative target
DNA analysis. This AFM-based DNA detection technique was three orders of magnitude more sensitive than a DNA detection method
based on UV-vis spectroscopy. 相似文献
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