On the Additive Property of Numerical Ranges

2020 ◽  
Vol 10 (03) ◽  
pp. 221-225
Author(s):  
然 许
Keyword(s):  
1999 ◽  
Author(s):  
Richard A. Gaggioli ◽  
David H. Richardson ◽  
Anthony J. Bowman ◽  
David M. Paulus

Abstract The concept of available energy, as defined by Gibbs (1873b) is revisited. He gave representations of available energy for two circumstances. The first was the available energy of a “body,” for the case when a body, alone, is in a nonequilibrium condition and therefore has energy available. In turn, he presented the available energy of “the body and medium,” for the energy which is available because a body is not in equilibrium with some arbitrarily specified medium. Gibbs’ representations were graphical. Since Gibbs, representations with formulas have been developed and are common, for the “available energy of body and medium.” Gaggioli (1998a, b) has developed formulas which are more general, to represent “the available energy of the body (alone)” and to assign an exergy to subsystems of the body as a measure of each sub-system’s contribution to the available energy. In contrast to the available energy, exergy is an additive property, so that balance equations can be written. And the formulas are independent from any “medium,” which is important both theoretically and practically — because of its relevance to proper selection of “the dead state.” These issues are discussed and extended, after reviewing Gibbs development of available energy and additional concepts which he introduced, such as “available vacuum” and “capacity for entropy.” It is argued that these “availabililty” and “capacity” concepts are all equivalent to one another. In turn, because of interconvertability, it is seen that available energy is something more fundamental than “maximum useful work.” Furthermore, it is illustrated that available energy, equilibrium and stability, and thermostatic property relations are relative, to “constraints.”


1969 ◽  
Vol 184 (1) ◽  
pp. 65-77 ◽  
Author(s):  
Klaus J�nich
Keyword(s):  

2004 ◽  
Vol 71 (2) ◽  
pp. 162-167 ◽  
Author(s):  
Jongwon Seok ◽  
Andrew T. Kim ◽  
Timothy S. Cale ◽  
John A. Tichy

A two-dimensional elastohydrodynamic analysis is performed on a system consisting of a viscous fluid flowing between a sliding soft layer of finite thickness and a tilted flat plate. The behavior of a soft layer subject to a distributed contact pressure is described in detail. Green’s functions are obtained for each Fourier coefficient of the distributed applied pressure, utilizing the additive property of linear elasticity theory. The resulting equations are numerically evaluated for some typical cases. As a function of the contact dimension, calculations are performed for the critical thickness of the layer beyond which the deformed shape essentially resembles that of the layer having an infinite thickness, in the case of a uniformly applied pressure. We also investigate the effect of layer thickness on the hydrodynamics, which illustrates that conditions in which the infinite half-space assumptions can be justified are highly limited. The findings of this paper have direct application to the modeling of chemical mechanical planarization (CMP).


2013 ◽  
Vol 46 (9) ◽  
pp. 754-759 ◽  
Author(s):  
Chuan Shi ◽  
Stanley B. Gershwin
Keyword(s):  

2014 ◽  
Vol 1033-1034 ◽  
pp. 521-525
Author(s):  
Cheng Ying Zhou ◽  
Wei Qu ◽  
Liu Lu Cai

This paper determined the total absorbance of phosphorus molybdenum blue and arsenic molybdenum blue by using the additive property of their absorbance values. By eliminating the interference of arsenic by reduction masking with composite reducing agent Na2SO3-Na2S2O3-KBr, the absorbance of phosphorus could be obtained. Thus, the content of phosphorus and arsenic could be calculated, respectively. The results show that the work curves of this method for phosphorus and arsenic are consistent with Beer’s law when the content of phosphorus and arsenic is 0-0.60ug/mL and 0-2.00ug/mL, respectively. The standard addition recovery rate of phosphorus and arsenic is 98.80%-101.04% and 99.00%-101.50%, respectively. The relative standard deviation of phosphorus and arsenic is less than 4.0% with good accuracy and precision. This method is simple and fast to determine phosphorus and arsenic in molybdenum concentrate, and the results are accurate and reliable.


2002 ◽  
Vol 124 (2) ◽  
pp. 105-109 ◽  
Author(s):  
Richard A. Gaggioli ◽  
David H. Richardson ◽  
Anthony J. Bowman

The concept of available energy, as defined by Gibbs is revisited. Being more general, this concept of available energy differs from that referred to commonly by the same name, or as “exergy” or “availability.” He gave representations of available energy for two circumstances. The first was the available energy of a “body,” for the case when a body, alone, is in a nonequilibrium condition and therefore has energy available. In turn, he presented the available energy of “the body and medium,” for the energy that is available because a body is not in equilibrium with some arbitrarily specified medium or “reference environment.” Gibbs’ did not present formulas to represent available energy. His representations were verbal descriptions regarding surfaces, curves and lines. Although his verbiage was augmented by some graphics, visualization of the geometrical entities he described depended largely on the imagination of the reader. In Part I, we take advantage of modern graphics software to illustrate more vividly not only the available energy he described verbally but also his interesting concepts of “available vacuum” and “capacity for entropy.” We argue that all of these concepts are equivalent. Since Gibbs, representations with formulas have been developed and are common for the “available energy of body and medium.” Gaggioli has developed formulas which are more general, to represent “the available energy of the body (alone)” and to assign an exergy to subsystems of the body as a measure of each subsystem’s contribution to the available energy. In contrast to the available energy, exergy is an additive property, so that balance equations can be written. This exergy is independent of any “reference environment,” which is important both theoretically and practically because of its relevance to proper selection of “the dead state.” In those special cases when the dead state is one in equilibrium with a “reference environment,” this more generalized exergy encompasses that concept called (today) exergy in textbooks and journals.


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