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41.
Tetrahedral amorphous hydrogenated carbon (ta-C:H) films with various substrate bias voltages were prepared using a magnetic-field-filter plasma stream deposition system. The microstructural and optical properties were studied using ellipsometric spectra. The refractive index n of each sample was obtained by simulating their ellipsometric spectral using Tauc-Lorentz oscillator model, and then the relative sp3 C ratio of each sample was calculated using Bruggeman effective medium approximation. The sp3 C fraction of each sample was quantified by using electron energy-loss spectroscopy (EELS). The blood compatibility of the samples was evaluated by tests of platelet adhesion, kinetic clotting time and thrombin time. The quantity and morphology of the adherent platelets on the surface of these samples were investigated using scanning electron microscopy. Results show that the spectroscopic ellipsometry is a helpful method to evaluate the sp3 carbon fraction of the carbon films. The substrate bias voltage has an obvious effect on sp3 content and blood compatibility of ta-C:H films. The sample prepared with substrate bias voltage of − 20 V showed the best blood compatibility. A simple bio-physical hypothetical model was proposed to explain the experiment results. 相似文献
42.
TiAl基合金在快速加热循环热处理过程中的结构失稳 总被引:2,自引:0,他引:2
观察了快速加热循环热处理过程中发生的4种结构失稳现象:形成二次层片组织、原始层片球化、晶界处非连续粗化、相界形核。通过比较连续加热与等温加热条件下的相转变开始线,探讨了连续加热与等温加热条件下结构失稳机制的异同。提出了快速加热循环热处理过程中避免结构失稳的途径:确保合金成分均匀,使各区域相变温度一致;使最高温度下的保温时间尽可能短。 相似文献
43.
In this paper the heteropoly complexes K_n[Ga(H_20)MW_(11)O_39)]·xH_20 [M=Cu(Ⅱ), Co(Ⅱ), Cr(Ⅲ),Fe(Ⅲ), Mn(Ⅳ)] have been prepared in this laboratory firstly. The products were characterized by chemicalanalysis, ionexchange, IR, UV and X-ray powder diffraction. 相似文献
44.
G. X. Zhao M. Zheng X. H. Lv X. H. Dong H. L. Li 《Metals and Materials International》2005,11(2):135-140
The corrosion behavior of 13Cr martensitic stainless steel in a CO2 environment in a stimulated oilfield was studied with potentiodynamic polarization and the impedance spectra technique. The
results showed that the microstructure of the surface scale clearly changed with temperature. This decreased the sensitivity
of pitting corrosion and increased the tendency toward general (or uniform) corrosion. The capacitance, the charge transfer
resistance, and the polarization resistance of the corrosion product scale decrease with increasing temperature from 90 to
120 °C, and thus the corrosion is a thermal activation controlled process. Charge transfer through the scale is difficult
and the corrosion is controlled by a diffusion process at a temperature of 150 °C. Resistance charge transfer through the
corrosion product layer is higher than that in the passive film. 相似文献
45.
R. Sarathi 《应用聚合物科学杂志》2002,83(13):2843-2849
In the present work tracking phenomena were studied with high‐density polyethylene (HDPE) materials under dc voltage, with NH4Cl and acid rain as contaminants. It was determined that the tracking time of the material depends on the conductivity and flow rate of the contaminant. Furthermore, physicochemical analysis by wide‐angle X‐ray diffraction studies, differential scanning calorimetry, and luminescence spectroscopy was carried out, whereupon it was concluded that the tracking process is a surface‐degradation process. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2843–2849, 2002; DOI 10.1002/app.10260 相似文献
46.
Andrew J. Morris Rebecca J. Nicholls Chris J. Pickard Jonathan R. Yates 《Computer Physics Communications》2014
We present OptaDOS, a program for calculating core-electron and low-loss electron energy loss spectra (EELS) and optical spectra along with total-, projected- and joint-density of electronic states (DOS) from single-particle eigenenergies and dipole transition coefficients. Energy-loss spectroscopy is an important tool for probing bonding within a material. Interpreting these spectra can be aided by first principles calculations. The spectra are generated from the eigenenergies through integration over the Brillouin zone. An important feature of this code is that this integration is performed using a choice of adaptive or linear extrapolation broadening methods which we show produces higher accuracy spectra than standard fixed-width Gaussian broadening. OptaDOS may be straightforwardly interfaced to any electronic structure code. OptaDOS is freely available under the GNU General Public licence from http://www.optados.org. 相似文献
47.
Ralph W. Howard C. A. McDaniel Dennis R. Nelson Gary J. Blomquist Leslie T. Gelbaum Leon H. Zalkow 《Journal of chemical ecology》1982,8(9):1227-1239
The cuticular hydrocarbon components of four castes ofReticulitermes virginicus (Banks) have been identified and quantitated. Components identified includen-alkanes; 2-, 3-, 11-, 13-, and 15-methyl-alkanes; 11,15-dimethylalkanes, (Z)-9-alkenes; (Z,Z)-7,9-dienes; and (E/Z)-6,9-dienes ranging in carbon number from C21 to C40. All caste forms ofR.virginicus contained the same components, but showed caste-specific proportions. Comparison of these hydrocarbons with those of the sympatric termiteR. flavipes (Kollar) suggest that cuticular hydrocarbons might serve as species- and caste-recognition cues. A bioassay was developed to test this species-recognition hypothesis, with the experimental results supporting the hypothesis.Isoptera: Rhinotermitidae. 相似文献
48.
The booklouse, Liposcelis bostrychophila, is an increasingly common pest of stored food products worldwide. We report here the cuticular lipid composition of this pest (the first report of the hydrocarbons of any member of the Order Psocoptera and the first report of fatty acid amides as cuticular components for any insect). No unsaturated hydrocarbons were present. A homologous series of n-alkanes (C21–C34), monomethyl alkanes (3-, 4-, 5-, 7-, 9-, 11-, 12-, 13- and 15-methyl-) with a carbon chain range of C28–C42, and dimethyl alkanes (3, 7-; 9, 13-; 11, 15-; 13, 17-; 9, 21-; 11, 19-; and 13, 21-); with a carbon number range of C31–C43 were identified. The relative abundances of these hydrocarbons were low, comprising approximately 0.0125% of total biomass. The amides were a homologous series (C16–C22 in chain length), with the major amide being stearoyl amide. In addition to the amides, free fatty acids (C16:1, C16:0, C18:2, C18:1, and C18:0 in chain length) and three straight chain aldehydes (C15, C16, and C17:1 in chain length) also occurred as cuticular components. These findings are discussed in terms of the chemical and physiological ecology of this species. 相似文献
49.
Jing Zhang 《Electrochimica acta》2006,51(20):4262-4270
A copolymer, poly(aniline-co-m-aminophenol), has been synthesized using repeated potential cycling. The monomer concentration ratio, acid concentration and applied potential strongly affect the copolymerization rate and the properties of the copolymer. The optimum conditions for the copolymerization are that the scan potential range is controlled between −0.10 and 0.95 V (vs.SCE), and a solution consists of 0.34 M aniline, 0.012 M m-aminophenol and 2 M H2SO4. The IR spectra of the copolymers demonstrate that the m-aminophenol units are included in the copolymer chains. The cyclic voltammograms of the copolymers in 0.3 M Na2SO4 solution with various pH values were performed at the potential ranges from −0.20 to 0.80 V and at a scan rate of 60 mV s−1. The results indicate that the copolymer still hold 41.7% of the electrochemical activity when the copolymer electrode was transferred from a solution of pH 5.0 to a solution of pH 11.0 in the potential range of −0.20 to 0.80 V. An impedance plot of the copolymer in a solution with pH 12.0 and at 0.40 V is constructed of a semicircle and a Warburg line with a slope of 1. This means that the electrode reaction of the copolymer at pH 12.0 is also under mass transfer control. The conductivity of the copolymer prepared under the optimum conditions is 1.42 S cm−1, and slightly depends on the pH value. Thus, the pH dependence of the electrical properties of the copolymer is improved compared with poly(aniline-co-o-aminophenol), and is much better than that of the parent polyaniline. 相似文献
50.
1-苯基-3-甲基-4-咔唑-N-丁基-4-苯甲酰基呲唑啉-5-酮的合成及其光谱研究 总被引:4,自引:0,他引:4
在苯和50%NaOH介质中,80℃时1,4-二溴丁烷与咔唑(CZ)反应,生成N-溴丁基咔唑(BCZ)。在丙酮和K2CO2介质中,50℃时N-溴丁基咔唑与1-苯基-3-甲基-4-苯甲酰基吡唑啉-5-酮(PMBP)反应,生成1-苯基-3-甲基-4-咔唑-N-丁基-4-苯甲酰基吡唑啉-5-酮(PMCBP),详细研究了CZ,BCZ,PMBP和PMCBP的UV和IR光谱.在氯仿中PMCBP对Nd(Ⅲ)的萃取率是PMBP的2.3倍,PMBP-Nd(Ⅲ)配合物无荧光,但PMCBP-Nd(Ⅲ)配合物有很强的荧光,说明PM-CBP是Nd(Ⅲ)的优良荧光试剂。 相似文献