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61.
本文综合啮合原理、微分几何和弹性力学的基础理论,对剃齿过程中刀具齿面和被剃齿轮齿面间的失配进行了分析。最后利用径向力求出了齿面间的压切量,从而解释并验证了剃齿过程中产生的齿形中凹现象。这对提高剃齿精度、降低噪音有着重要意义。 相似文献
62.
Tomasz Rolski 《Queueing Systems》1989,4(1):17-26
We study single server periodic queues in the day equilibrium conditions. The following characteristics of interest are considered at time of dayt: Vp(t)-the work load, Lp(t)-the number of customers and up(t)-the departure rate. We give relationships between E[Vp(t)], E[Lp(t)] and up(t). We also prove that E[Vp(t)] < and E[Lp(t)] < provided the second moment of the service time is finite. 相似文献
63.
陶华学 《山东科技大学学报(自然科学版)》1988,(4)
应用模糊数学方法研究和处理矿山测量中存在的具有“模糊性”的问题。例如控制网布设方案及矿山测量图纸质量的综合评判。它能更准确地描述用精确数学模型难以描述的问题。 相似文献
64.
熊楚强 《北京科技大学学报》1988,(4)
本文从热力学第二定律的基本原理出发,概要地总结了论证“最大功原理”的方法,进而讨论了热力学中的一些基本问题。其基本思想是:分析热力学问题切不可忘了环境。由此得出了某些有意义的结论,澄清了在学习热力学过程中人们常产生的一些疑惑。 相似文献
65.
稀土复合变质对新型铸造热锻模具钢组织与性能的影响 总被引:8,自引:1,他引:8
研究了稀土复合变质对新型铸造热锻模具钢(CHD钢)组织与性能的组织。结果表明,稀土复合变质能细化晶粒,并且随着稀土量的增加。细化效果明显;加入适量的稀土复合变质后,夹杂物数量明显减少,夹杂物趋于球化并均匀地分布在钢中,形态和分布得以了改善,向钢中加入稀土进行复合变质,能促进贝氏体、奥氏体和位错亚结构的形成,细化马氏体板条。当残留稀土含量为0.02%时,CHD钢的硬度、强度变化不大,断裂韧性(KIC)和疲劳裂纹扩展门槛值(△Kth)有所提高,冲击韧性、延伸率、断面收缩率提高了近一倍,抗热疲劳性能也最好。 相似文献
66.
聚丙烯/POE共混组成对材料断裂行为的影响 总被引:1,自引:0,他引:1
采用基本断裂功(EWF)方法对聚丙烯(PP)/聚烯烃弹性体(POE)共混物的注射双边缺口拉伸试样的断裂行为进行了研究,比较了不同POE含量对共混物各断裂参数的影响.结果表明,PP和用量为5phr POE的共混物都可完全满足EWF方法的要求,共混物的断裂韧性-比基本断裂功we,较PP有显著提高;POE用量为10phr以上的共混物则出现明显的成颈现象而限制了EWF方法的应用;PP和各种POE用量的共混物都得到了其屈服所需要的比基本断裂功we,y和比塑性功β′wp,y. 相似文献
67.
Thomas P J Linsinger Alexander Bernreuther Philippe Corbisier Marta Dabrio Håkan Emteborg Andrea Held Andrée Lamberty Gaida Lapitajs Marina Ricci Gert Roebben Stefanie Trapmann Franz Ulberth Hendrik Emons 《Accreditation and quality assurance》2007,12(3-4):167-174
The potential approaches for third-party assessment of reference material producers are revisited and the activities of the
Reference Materials (RM) Unit of the Institute for Reference Materials and Measurements (IRMM) to obtain accreditation to
ISO Guide 34 and ISO 17025 are described. Accreditation was related to the Unit as all matrix RM activities of the institute
are concentrated there. A management system was established that allows sufficient flexibility to be applicable to a wide
range of RMs while being precise enough to ensure compliance with ISO Guides 30, 31 and especially 34 and 35. Accreditation
was achieved in 2004 with independent scopes for testing and RM production and was confirmed and extended in 2005. The key
aspects of the RM Unit's management system for RM production are presented.
Presented at BERM-10, April 2006, Charleston, SC, USA 相似文献
68.
Paul W. Chun 《International journal of quantum chemistry》2001,85(6):697-712
This communication will demonstrate the existence of a thermodynamic molecular switch in the pairwise, sequence‐specific hydrophobic interaction of Ile–Ile, Leu–Ile, Val–Leu, or Ala–Leu over the temperature range of 273–333 K reported by Nemethy and Scheraga in 1962. Based on Chun's development of the Planck–Benzinger methodology, the change in inherent chemical bond energy at 0 K, ΔH°(T0), is 3.0 kcal mol?1 for Ile–Ile, 2.4 for Leu–Ile, 1.8 for Val–Leu, and 1.2 kcal mol?1 for Ala–Leu. The value of ΔH°(T0) decreases as the length of the hydrophobic side chain decreases. It is clear that the strength and stability of the hydrophobic interaction is determined by the packing density of the side chains, with Ala–Leu being the most stable. At 〈Tm〉, the thermal agitation energy, $\int^{T}_{0}\Delta Cp^{\circ}(T)\,dT$, is about five times greater than ΔH°(T0) in each case. Additionally, the thermal agitation energy for the same series, evaluated at 〈Tm〉, decreases in the same order, that is, as the length of the side chain decreases. This pairwise, sequence‐specific hydrophobic interaction is highly similar in its thermodynamic behavior to that of other biological systems, except that the negative Gibbs free energy change minimum at 〈Ts〉 occurs at a considerably higher temperature, 355 K compared to about 300 K. The melting temperature, 〈Tm〉, is also high, 470 K compared to 343 K in a biological system. The implication is that the negative Gibbs free energy minimum at a well‐defined 〈Ts〉 has it origin in the hydrophobic interactions, which are highly dependent on details of molecular structure. In addition to the four specific dipeptide interactions described, we have shown in our unpublished work the existence of a thermodynamic molecular switch in the interactions of 32 dipeptides wherein a change of sign in ΔCp°(T)reaction leads to a true negative minimum in the Gibbs free energy of reaction, and hence, a maximum in the related Keq. Indeed, all interacting biological systems that we have thus far examined using the Planck–Benzinger approach point to the universality of thermodynamic molecular switches. © 2001 John Wiley & Sons, Inc. Int J Quantum Chem, 2001 相似文献
69.
Rashid A. Zeineh George Kyriakidis Roger Acey Christopher Smith 《Applied biochemistry and biotechnology》1986,13(2):119-125
Citrus tristeza virus (CTV) extracted from Etrog citron (C.medica L.) was immunoprecipitated. The immunoprecipitate was fractionated by SDS-PAGE and western blotted onto nitrocellulose. The CTV
antigens were determined by immunoblot analysis using rabbit anti-CTV IgG, and the protein-band pattern exhibited on the nitrocellulose
was assessed by soft-laser scanning densitometry. The densitometric tracing revealed the presence of bands that were not visible
to the naked eye. Using the superimposition mode of the instrument, it was also revealed that the protein-band patterns of
different CTV samples were not identical. Computer-aided soft-laser scanning densitometry proved to be a powerful approach
in the detection and assessment of protein bands revealed on nitrocellulose immunoblots, which we were previously unable to
do employing conventional methods. 相似文献
70.
The plastic deformation mechanism operating in polymer glasses is analyzed. The whole process consists of two main stages: nucleation of special shear defects, called PSTs (plastic shear transformations), and their disappearance. The important feature of plastic deformation of glasses is the storage of a large amount of internal energy ΔUdef upon straining. Such energy storage is the critical issue for mechanical performance of polymeric material: if the amount of stored energy is high, the appearance of macroscopic failure is very probable while glassy materials collecting a small amount of stored deformation energy are quite ductile. It is proposed that the rate of disappearance of PSTs is a key factor in dissipation of stored deformation energy. A parameter describing the dissipation ability of material upon deformation is introduced. 相似文献