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51.
本文介绍了磁电机点火系统的点火提前角测量原理。对点火系统的点火信号和触发信号进行采集、调理,再用单片机进行处理,最后用LabVIEW进行点火提前角数据存储和显示。 相似文献
52.
本文介绍了HSDPA的发展背景,针对HSDPA的主要技术特点,依据市场发展规划、用户需求等方面对HSDPA部署进行探讨,并对HSDPA的覆盖与容量方面进行规划分析. 相似文献
53.
Hydrate formation rate plays an important role in making hydrates for the storage and transport of natural gas. Micellar surfactant solutions were found to increase gas hydrate formation rate and storage capacity. With the presence of surfactant, hydrate could form quickly in a quiescent system and the energy costs of hydrate formation reduced. Surfactants (an anionic surfactant, a non‐ionic surfactant and their mixtures) and liquid hydrocarbons (cyclopentane and methylcyclohexane) were used to improve hydrate formation. The experiments of hydrate formation were carried out in the pressure range 3.69–6.82 MPa and the temperature range 274.05–277.55 K. The experimental pressures were kept constant during hydrate formation in each experimental run. The effect of anionic surfactant (sodium dodecyl sulphate (SDS)) on natural gas storage in hydrates is more pronounced compared to a non‐ionic surfactant (dodecyl polysaccharide glycoside (DPG)). The induction time of hydrate formation was reduced with the presence of cyclopentane (CP). Cyclopentane and methylcyclohexane (MCH) could increase hydrate formation rate, but reduced hydrate storage capacity The higher methylcyclohexane concentration, the lower the hydrate storage capacity. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
54.
Guo Haitao Qiao Weihong Ba Yan Li Zongshi Jin Kun Peng Qinji 《Petroleum Science and Technology》2006,24(1):51-60
The GC/MS and NMR analysis of the reaction products of naphthalene with 1-bromohexane were reported. The products obtained were suggested to have six isomers of linear hexylnaphthalene and the structure of each isomer was determined by GC/MS and NMR spectra. For the first time, the unique chemical shift data were obtained. The content of each isomer calculated by 1H NMR and 13C NMR spectra was consistent with that by GC/MS spectra, which confirmed the accuracy of NMR data. 相似文献
55.
本文主要是在线性解调系统中,利用信道中加性高斯白噪声正交分量(nc与Ns)两者正交性与其中之一(ns)经相移之后形成线性相关性使噪声本身消除噪声,以达到提高信噪比的目的,从而提高抗噪声性能. 相似文献
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Sun Qing-Ping Guo Tian-Fu Li Xue-Jun Zhang Xing 《International Journal of Fracture》1996,78(3-4):315-330
Numerical study by the finite element method (FEM) is performed to investigate the effect of dual-scale microstructure on the toughness of laminar zirconia composite. The computation is based on the micromechanics constitutive model of polycrystal transformation plasticity developed by Sun et al. [10] where both transformation induced shear and softening effects during autocatalytic transformation are taken into account. The numerical simulation presented in this paper successfully reproduced the experimentally observed two effects of the dual-scale microstructure on the toughness of laminar zirconia composite, i.e., the truncation of the elongated transformation frontal zone that forms in single phase Ce-ZrO2 and the propagation of the transformation zone along the layers normal to the crack plane. Quantitative analysis on the role of microstructure in transformation toughening of laminar zirconia composite is first carried out in the present work which will provide a starting point for the microstructural design of this novel advanced composite in the future.Presented at the Far East Fracture Group (FEFG) International Symposium on Fracture and Strength of Solids. 4–7 July 1994 in Xi'an, China. 相似文献
60.
Previously, we showed that the N-terminal recognition domain (T1) of Kv1.3 was not required for assembly of functional channels [Tu et al. (1996) J. Biol. Chem. 271, 18904-18911]. Moreover, specific Kv1.3 peptide fragments including regions of the central core are able to inhibit expression of current produced from a channel lacking the T1 domain, Kv1.3(T1-). To elucidate the mechanism whereby Kv1.3 peptide fragments suppress Kv1.3(T1-) current, we have studied the ability of peptide fragments containing the transmembrane segments S1, S1-S2, or S1-S2-S3 to physically associate with the Kv1.3(T1-) polypeptide subunit in vitro in microsomal membranes. Using c-myc (9E10) epitope-labeled peptide fragments and anti-myc antibody as well as antisera to the Kv1.3 C-terminus, we now demonstrate specific association of these peptide fragments with Kv1.3(T1-). Association of peptide fragments with Kv1.3(T1-) was correlated with integration of both proteins into the membrane. Furthermore, the relative strength and kinetics of this association directly correlated with the ability of fragments to suppress Kv1.3(T1-) current. The rate-limiting step in the sequential synthesis, integration, and formation of a complex was the association of integrated polypeptides within the plane of the lipid bilayer. These results strongly suggest that the physical association of transmembrane segments provides the basis for suppression of K+ channel function by K+ channel peptide fragments in vivo. Moreover, the S1-S2-S3 peptide fragment potently suppressed full-length Kv1.3, thus implicating a role for the S1-S2-S3 region of Kv1.3 in the assembly of the Kv1.3 channel. We refer to these putative association sites as IMA (intramembrane association) sites. 相似文献