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951.
952.
从液氮温度到水的沸点温度范围内,测量了介质分别为钽,涤纶,陶瓷,玻璃釉和陶瓷独石一体化结构的商用固体电容器的电容量-温度之间的关系.拟合测量结果表明,独石陶瓷电容器在正温度段具有较好的线性响应(-10pF/℃),灵敏度(0.1 ℃)和精确度(标准差为0.016);而涤纶电容器在负温度段的特性较好( 17pF/℃,0.06 ℃和0.01).此外,在约0.5特斯拉的恒定磁场作用下,无论在正或负温度段,上述测得的电容量-温度关系几乎不受影响.因此,本研究对开发抗强电磁场,自加热效应小或导热系数小的低温测温器具有较大的参考价值. 相似文献
953.
The CO2-broadened water coefficients (half-widths, line shifts, and temperature dependence of the widths) are predicted using a fully complex Robert-Bonamy formulation for the 937 allowed and forbidden perpendicular type transitions of (000)-(000) between 200 and 900 cm−1 in order to facilitate atmospheric remote sensing of Mars and Venus. In addition, empirical Lorentz line widths and pressure-induced frequency-shifts of CO2-broadened H216O are obtained at room temperature for 257 perpendicular transitions of the (010)-(000) fundamental. For this, calibrated spectra recorded at 0.0054 cm−1 resolution are measured assuming Voigt line shapes. For transitions between 1287 and 1988 cm−1 with rotational quanta up to J = 13 and Ka = 6, the widths vary from 0.045 to 0.212 cm−1 atm−1 at 300 K; the pressure-shifts are quite large and range from −0.0386 to +0.0436 cm−1 atm−1. For the (010)-(000) band, the RMS and mean observed and calculated differences for CO2-broadened H2O half-widths are 12% and −1.9%, respectively, while the RMS and mean ratios of the observed and calculated pressure-induced shift coefficients are 1.6 and 0.79, respectively. For pairs of transitions involving Ka = 0 and 1, such as 20 2 ← 31 3 and 31 3 ← 20 2, both the calculated and observed pressure induced shifts in positions are opposite in sign and often similar in magnitude. The data are too limited to characterize vibrational dependencies of the widths, however. 相似文献
954.
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
955.
Wang-bing Zhang Xin-an Yang Yuan-yuan Ma Hai-xia Zhu Shang-bing Wang 《Microchemical Journal》2011,97(2):201-206
The determination of trace concentrations of Hg in water samples by the use of electrolytic cold vapor generation (ECVG) system and AFS was studied. Several buffer solutions were used and the detection limits with these systems were found to be by a factor of 1–2 lower than in the conventional electrolytic cold vapor generation system. Comparing with the traditional inorganic acid, phosphate buffer solution (PBS) increased the signal intensity of Hg vapor from electrolytic generation on Pt cathode and reduced the impact of cathode erosion on the stability of signal intensity. Moreover, buffer solution has better interference tolerance. The effects of the electrolytic conditions and interference ions on the ECVG have been studied. Under optimized conditions and with PBS as catholyte the detection limit for Hg was found to be 0.27 ng L−1. The relative standard deviation was 2.8% for 11 consecutive measurements of 1 μg L−1 Hg. This method has been applied in the determination of inorganic Hg in Yangtze River water. 相似文献
956.
Eric Morssing Vilén Markus Klinger Corine Sandström 《Magnetic resonance in chemistry : MRC》2011,49(9):584-591
Alginate is a linear copolymer of 1‐4 linked β‐D ‐mannuronic acid (M) and 1‐4 linked α‐L ‐guluronic acid (G). The physical properties of these polysaccharides such as gel properties and viscosity are largely correlated to the monomer composition (M/G ratio), the sequence of the polymer and the molecular weight. Determination of the M/G ratio is therefore important and NMR spectroscopy is among the most common methods used to accurately obtain this ratio. Instead of using time consuming, possibly sample altering, acid hydrolysis to reduce the viscosity of the alginate sample prior to analysis, samples of low concentrations can be used. However, this results in a water peak in the NMR spectrum that is several orders of magnitude larger than the alginate signals and water suppression is required. In this article, a diffusion‐edited NMR experiment that suppresses the water peak while retaining the signals of interest has been used to enable correct M/G ratio determination. This approach exploits the difference in translational diffusion between the larger alginate molecules and the smaller water molecules. Using this method, the monomer composition of 20 different alginate powders was determined. The diffusion parameters were optimized to allow measurement for samples covering a large range of M/G ratios and viscosities. Thus, such method should be useful for analyzing large numbers of unknown alginate samples using, for example, automation procedures. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
957.
Shin‐Ichi Yusa Shigeki Awa Masanori Ito Takeshi Kawase Tadao Takada Kenichi Nakashima Dian Liu Shigeru Yamago Yotaro Morishima 《Journal of polymer science. Part A, Polymer chemistry》2011,49(13):2761-2770
Water‐soluble diblock copolymer, poly(N‐isopropylacrylamide)‐block‐poly(N‐vinyl‐2‐pyrroridone) (PNIPAMm‐b‐PNVPn), was found to associate with fullerene (C60), and thus C60 can be solubilized in water. The 63C60/PNIPAMm‐b‐PNVPn micelle formed a core‐shell micelle‐like aggregate comprising a C60/PNVP hydrophobic core and a thermoresponsive PNIPAM shell. The C60‐containing polymer micelle formation and its thermoresponsive behavior were characterized using light scattering and 1H NMR techniques. The hydrodynamic radius (Rh) of the C60‐bound polymer micelle increased with increasing temperature, which was ascribed to the hydrophobic association between dehydrated PNIPAM shells above lower critical solution temperature (LCST). 1H NMR data suggest that the motion of the PNIPAM block is restricted above LCST due to the dehydration of the PNIPAM shell in water. The generation of singlet oxygen by photosensitization by the C60‐bound polymer micelle was confirmed from photooxidation of 9,10‐anthracenedipropionic acid. Furthermore, DNA was found to be cleaved by visible light irradiation in the presence of the C60‐bound polymer micelle. Therefore, there may be a hope for a pharmaceutical application of the C60‐bound polymer micelle to cancer photodynamic therapy. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011. 相似文献
958.
Lin Gu Xianhong Wang Xuesi Chen Xiaojiang Zhao Fosong Wang 《Journal of polymer science. Part A, Polymer chemistry》2011,49(24):5162-5168
Aliphatic poly(urethane‐amine) (PUA) was synthesized from copolymerization of CO2 and 2‐methylaziridine (MAZ) using Y(CCl3COO)3‐ZnEt2‐glycerine coordination catalyst, the urethane content of PUA was over 80%, and its yield could reach 90%. PUA with molecular weight as high as 31.0 kg/mol was obtained when the copolymerization reaction was carried out in N,N‐dimethylacetamide (DMAc), mainly due to the good solubility of PUA in DMAc. PUA exhibited reversible thermo‐responsive property in deionized water, and the lower critical solution temperature (LCST) was highly sensitive to its urethane content and molecular weight, which was observed in a broad window from 37 to 90 °C. Furthermore, the phase transition behavior could also be controlled by change of pH value. When the pH value of the PUA aqueous solution changed from 9.2 to 13, the LCST value of the solution decreased from 48.4 °C to 30 °C. Therefore, the PUA showed thermo‐ and pH‐ dual responsive performance in water. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
959.
Valerio Caleffi 《国际流体数值方法杂志》2011,67(9):1135-1159
Hermite weighted essentially non‐oscillatory (HWENO) methods were introduced in the literature, in the context of Euler equations for gas dynamics, to obtain high‐order accuracy schemes characterized by high compactness (e.g. Qiu and Shu, J. Comput. Phys. 2003; 193 :115). For example, classical fifth‐order weighted essentially non‐oscillatory (WENO) reconstructions are based on a five‐cell stencil whereas the corresponding HWENO reconstructions are based on a narrower three‐cell stencil. The compactness of the schemes allows easier treatment of the boundary conditions and of the internal interfaces. To obtain this compactness in HWENO schemes both the conservative variables and their first derivatives are evolved in time, whereas in the original WENO schemes only the conservative variables are evolved. In this work, an HWENO method is applied for the first time to the shallow water equations (SWEs), including the source term due to the bottom slope, to obtain a fourth‐order accurate well‐balanced compact scheme. Time integration is performed by a strong stability preserving the Runge–Kutta method, which is a five‐step and fourth‐order accurate method. Besides the classical SWE, the non‐homogeneous equations describing the time and space evolution of the conservative variable derivatives are considered here. An original, well‐balanced treatment of the source term involved in such equations is developed and tested. Several standard one‐dimensional test cases are used to verify the high‐order accuracy, the C‐property and the good resolution properties of the model. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
960.
The nature of the strong hydrogen bonds found in p-cresol/formaldehyde (PCF) resins, compared to ordinary phenolic compounds, is studied. The evidence from FTIR spectroscopy indicates that this strong interaction is due to intramolecular hydrogen bonding from “calixarene-like” structures. The formation of this structure in PCF is enabled by its “linear” (all-ortho-linkage) structure, which is not present in branched resins. Additionally, a transition is observed at around 175 to 200°C where the intramolecular hydrogen bonded structure is lost. This structure cannot be recovered upon cooling or annealing due to restrictions on conformational rotations that are coupled to a new pattern of intermolecular hydrogen bonding. However, the structure is reformed by dissolving the resin in solution and casting new films. 相似文献