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Physical Properties and Phenomena

The viscosity of nonliving systems (13,38) and protoplasm (81) has been so thoroughly and so often reviewed that it will be sufficient here to refer briefly to some recent work. [Pg.36]

Many competent investigators regard viscosity as one of the most significant of protoplasmic properties. On it, they say, do such basic activities as amoeboid movement, cyclosis, and metabolism depend but this is only indirectly true. It is contractility and not viscosity on which protoplasmic movement primarily depends the two properties are independent variables. Viscosity plays its ]iart in protoplasmic movement, but it is not a cause. If the force responsible remains constant, the rate of movement will be inversely proportional to the viscosity of the protoplasm but, if the motive force varies, the rate of flow will vary in direct proportion to it, and the viscosity need not change at all. The situation is similar in the case of metabolism viscosity plays a secondary part. Lh6risson (44) has pointed out that metabolic rate is inversely proportional to viscosity. He bases this conclusion on the fact that the rate of chemical reactions is dependent upon diffusion and rate of diffusion is proportional to viscosity. [Pg.37]

Anomalous osmosis presents a similar situation. We expect a certain result, namely, the movement of a liquid in conformity with the laws of diffusion, and get instead movement in the reverse direction so again we say, anomalous osmosis. But again it is some other force, of which we are unaware, which upsets the expected situation and causes diffusion against a concentration gradient. The anomalous osmosis is in full obedience to some other force, which may be an electric potential. [Pg.37]

Once an anomalous situation is understood it ceases to be disturb- [Pg.37]

Anomalous viscosity has revealed more of the structure of fluids, and of such physical properties as birefringence, elasticity, and thixotropy, than any other single physical characteristic. The physicist had stated the laws of normal flow, but it remained for the colloid chemist to investigate the non-Newtonian, nonlawful fluids which exhibit anomalous viscosity. The Society of Rheology was a direct result of interest in the non-Newtonian behavior of liquids. Indeed, it may well be said that the raison d etre of colloid chemistry is the digression of physical apd chemical systems from classical laws. [Pg.38]


Behavior. Diffusion, Brownian motion, electrophoresis, osmosis, rheology, mechanics, and optical and electrical properties are among the general physical properties and phenomena that are primarily important in coUoidal systems (21,24—27). Of course, chemical reactivity and adsorption often play important, if not dominant, roles. Any physical and chemical feature may ultimately govern a specific industrial process and determine final product characteristics. [Pg.394]

AccuracyAJncertainty The lack of specific data on component failure characteristics, chemical and physical properties, and phenomena severely limit accuracy and can produce large uncertainties. [Pg.46]

The static dipole polarizability is the linear response of an atomic or molecular system to the application of a weak static electric field [1], It relates to a great variety of physical properties and phenomena [2-5]. Because of its importance, there have been numerous ab initio calculations of isolated atomic and molecular polarizabilities [6-14]. Particular theoretical attention has been dedicated to the polarizability of free atomic anions [15-21] because of its fragility and difficulty in obtaining direct experimental results. In recent years theoretical studies have... [Pg.141]

The choice of the force field is the key to accurate results that reproduce or predict physical properties and phenomena in the system under study. The forces acting on the nuclei are derived from the gradients of the potential energy function... [Pg.234]

Once the unit is running well, it is often assumed that the aeration system is sized properly, but changes in the catalyst physical properties and/or catalyst circulation rate may require a different purge rate. It should be noted that aeration rate is directly proportional to catalyst circulation rate. Trends of the E-cat properties can indicate changes in the particle size distribution, which may require changes in the aeration rate. Restriction orifices could be oversized, undersized, or plugged with catalyst, resulting in over-aeration, under-aeration, or no aeration. All these phenomena cause low pressure buildup and low slide valve differential. [Pg.242]

In many respects, this is the kernel of this book. For years it has not been too clear how one could consistently account for the wide variety of transition-metal chemistry in a way that does not conflict with the equally varied phenomena of spectroscopy and magnetochemistry that are so well rationalized by ligand-field theory. There is a tendency - psychologically quite natural, no doubt - for those interested in synthetic and mainstream chemistry not to look too closely at theory and physical properties, and, of course, vice versa. However, there has always been the need, surely, to build a logical synthesis of, or bridge between, these two aspects of the same subject. We hope that our presentation in this book goes some way towards providing that overview. [Pg.128]

The examples that follow assume constant physical properties and use Equation (5.28). Their purpose is to explore nonisothermal reaction phenomena rather than to present detailed design calculations. [Pg.167]

Phosphorus is one of the most remarkable of the many remarkable substances known to the chemist. The curious method of its discovery, the universality of its distribution, its intimate connection with the phenomena of animal and vegetable life, its extraordinary physical properties and chemical activity, its abnormal molecular constitution, the protean ease of its allotropie transformation, all combine to make up a history which abundantly justifies its old appellation of the phosphorus miraibilia.—T. E. Thorpe. [Pg.729]

The manufacture of products by reactive molding results in the superposition of interrelated chemical and physical phenomena. These include polymerization, crystallization, vitrification, heat transfer, rheokinetic effects, changes in the physical properties and volume of a material injected into a mold. It is quite natural that special experimental methods are required to study and control the complex processes which take place in molds. [Pg.97]

IC Khoo. Liquid crystals Physical Properties and Nonlinear Optical Phenomena. New York Wiley, 1995. [Pg.360]

Figure 3.29 Illustrations of changes occurring in physical properties and other phenomena in the region of the optimal salinity for enhanced oil recovery using surfactant flooding. From Sharma [235]. Copyright 1991, Plenum Press. Figure 3.29 Illustrations of changes occurring in physical properties and other phenomena in the region of the optimal salinity for enhanced oil recovery using surfactant flooding. From Sharma [235]. Copyright 1991, Plenum Press.
The reactions considered in previous sections have involved hypothetical components A, B, C, and I) for which arbitrary physical properties and kinetics could be selected to illustrate various phenomena. Simple Matlab programs can be easily generated for these systems. [Pg.72]

Successful model building is at the very heart of modern science. It has been most successful in physics but, with the advent of quantum mechanics, great inroads have been made in the modelling of various chemical properties and phenomena as well, even though it may be difficult, if not impossible, to provide a precise definition of certain qualitative chemical concepts, often very useful ones, such as electronegativity, aromaticity and the like. Nonetheless, all successful models are invariably based on the atomic hypothesis and quantum mechanics. The majority, be they of the ah initio or semiempirical type, is defined via an appropriate non-relativistic, Born-Oppenheimer electronic Hamiltonian on some finite-dimensional subspace of the pertinent Hilbert or Fock space. Consequently, they are most appropriately expressed in terms of the second quantization formalism, or even unitary group formalism (see, e.g. [33]). [Pg.483]

Khan, M.I., Tabussum, S., and Doedens, R.J., Chem. Commun., 532, 2003. Riddick, J.A., Bunger, W.B., and Sakano, T.K., Organic Solvent Physical Properties and Methods of Purification, 4th ed., John Wiley Sons, New York, 1986. Amis, E.S., and Hinton, J.R, Solvent Effects on Chemical Phenomena, Academic Press, New York, 1973. [Pg.325]


See other pages where Physical Properties and Phenomena is mentioned: [Pg.273]    [Pg.231]    [Pg.35]    [Pg.36]    [Pg.128]    [Pg.273]    [Pg.231]    [Pg.35]    [Pg.36]    [Pg.128]    [Pg.947]    [Pg.739]    [Pg.272]    [Pg.337]    [Pg.354]    [Pg.417]    [Pg.210]    [Pg.126]    [Pg.92]    [Pg.1327]    [Pg.8]    [Pg.97]    [Pg.200]    [Pg.319]    [Pg.173]    [Pg.308]    [Pg.7]    [Pg.262]    [Pg.683]    [Pg.133]    [Pg.3]    [Pg.613]    [Pg.948]    [Pg.428]   


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