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Interactions between

Although the composite curves can be used to set energy targets, they are not a suitable tool for the selection of utilities. The grand composite curve is a more appropriate tool for understanding the interface between the process and the utility system. It is also, as is shown in later chapters, a useful tool for study of the interaction between heat-integrated reactors and separators and the rest of the process. [Pg.185]

Interactions between the reactor and the rest of the process are extremely important. Reactor conversion is the most significant optimization variable because it tends to influence most operations through the process. [Pg.252]

Economic tradeoffs. Interactions between the reactor and the rest of the process are extremely important. Reactor conversion is the most significant optimization variable because it tends to influence most operations through the process. Also, when inerts are present in the recycle, the concentration of inerts is another important optimization variable, again influencing operations throughout the process. ... [Pg.402]

Langmuir adsorption isotherm A theoretical equation, derived from the kinetic theory of gases, which relates the amount of gas adsorbed at a plane solid surface to the pressure of gas in equilibrium with the surface. In the derivation it is assumed that the adsorption is restricted to a monolayer at the surface, which is considered to be energetically uniform. It is also assumed that there is no interaction between the adsorbed species. The equation shows that at a gas pressure, p, the fraction, 0, of the surface covered by the adsorbate is given by ... [Pg.234]

Although still used the Langmuir equation is only of limited value since in practice surfaces are energetic inhomogeneous and interactions between adsorbed species often occur. [Pg.234]

Raoult s law When a solute is dissolved in a solvent, the vapour pressure of the latter is lowered proportionally to the mole fraction of solute present. Since the lowering of vapour pressure causes an elevation of the boiling point and a depression of the freezing point, Raoult s law also applies and leads to the conclusion that the elevation of boiling point or depression of freezing point is proportional to the weight of the solute and inversely proportional to its molecular weight. Raoult s law is strictly only applicable to ideal solutions since it assumes that there is no chemical interaction between the solute and solvent molecules. [Pg.341]

Ziegler catalysts Complex catalysts prepared by interaction between an organometallic derivative and a transition metal derivative. A typical catalyst is the product of the interaction of TiCU and AIBU3. These catalysts polymerize olefins, particularly ethylene, to polyolefins, the polymerization generally being in a siereoregular manner. [Pg.432]

The higher the eluting force of the solvent, the more easily the components are desorbed. This force is represented by the solvent s polarity which results in mainly three types of interaction between the solvent and the solute ... [Pg.26]

The more-or-less pronounced interactions between the added component and the receiving system are identified, for example, as follows ... [Pg.206]

Viscosity additives are aliphatic polymers of high molecular weight whose main chain is flexible. It is known that in a poor solvent, interactions between the elements making up the polymer chain are stronger than interactions between the solvent and the chain (Quivoron, 1978), to the point that the polymer chain adopts a ball of yarn configuration. The macromolecules in this configuration occupy a small volume. The viscosity of a solution being related to the volume occupied by the solute, the effect of polymers on the viscosity in a poor solvent will be small. [Pg.355]

Consider that at low temperatures, a lubricant is a poor solvent for polymer chains. When the temperature increases, interactions between polymer chains decrease the space occupied by the polymer ball takes on greater volume and consequently, the viscosity decrease due to the lubricant temperature increase is compensated by the unfolding of the polymer chain and the result is a reduction of the difference between the viscosities at low and high temperature, and therefore an Increase in viscosity index. [Pg.355]

Polymethacrylates are less soluble than hydrocarbon polymers in mineral oils, they thicken less at low temperatures and are more effective at high temperatures. In this respect, it is important to note that the modification of rheoiogical properties is based on interactions between polymer and oil it will therefore be always dependent of the nature of oil. [Pg.356]

Imagine for a moment that the exploration activities carried out in the previous section have resulted in a successful discovery well. Some time will have passed before the results of the exploration campaign have been evaluated and documented. The next step will be the appraisal of the accumulation, and therefore at some stage a number of additional appraisal wells will be required. The following section will focus on these drilling activities, and will also investigate the interactions between the drilling team and the other E P functions. [Pg.29]

The choice of drilling fluid has a major impact on the evaluation and" production of a well. Later in this section, we will investigate the interaction between drilling fluids, logging operations and the potential damage to well productivity caused by mud invasion into the formation. [Pg.40]

The comparison between measured data and simulated data are good for both real and imaginary parts. The measured signal has a low resolution due to the low interaction between the eddy current and the slot. [Pg.144]

NDT inspection in the thin-skin regime is well adapted to finding the length of a surface slot or crack from eddy current data. With the electromagnetic skin depth smaller than the slot depth, the interaction between the eddy current induced in the test block and tbe slot is strong at the surface of the block. [Pg.145]

According to some remarks concerning the physical interaction between the incident ultrasonic wavelet and the defects [4-6], we consider that an Ascan signal, may be described as a weighted sum of few delayed and phase-shifted replicas of the ultrasonic incident wavelet j(r). We can express this mathematically as ... [Pg.174]

Theoretical studies of the interaction between an ultrasonic beam and planar defects have been widely carried out and shown that the upper and lower tip diffraction echoes are characterized by phase inversion. In other words, the measurement of 180° phase shift between these two echoes proves the plane nature of the defect that has generated them. [Pg.178]

For conventional probes, acoustic verification aims at characterizing the beam pattern, beam crossing, beam angle, sensitivity, etc., which are key characteristics in the acoustic interaction between acoustic beam and defect. For array transducers, obviously, it is also a meaning to check the acoustic capabilities of the probe. That is to valid a domain (angle beam, focus, etc.) in which the probe can operate satisfactorily. [Pg.822]

Equations II-12 and 11-13 illustrate that the shape of a liquid surface obeying the Young-Laplace equation with a body force is governed by differential equations requiring boundary conditions. It is through these boundary conditions describing the interaction between the liquid and solid wall that the contact angle enters. [Pg.13]

The surface free energy can be regarded as the work of bringing a molecule from the interior of a liquid to the surface, and that this work arises from the fact that, although a molecule experiences no net forces while in the interior of the bulk phase, these forces become unbalanced as it moves toward the surface. As discussed in connection with Eq. Ill-IS and also in the next sections, a knowledge of the potential function for the interaction between molecules allows a calculation of the total surface energy if this can be written as a function of temperature, the surface free energy is also calculable. [Pg.56]

As circular domains grow in size or number, the dipolar interactions between them increase until they form a hexagonal array of spacing... [Pg.139]

The influence of electrical charges on surfaces is very important to their physical chemistry. The Coulombic interaction between charged colloids is responsible for a myriad of behaviors from the formation of opals to the stability of biological cells. Although this is a broad subject involving both practical application and fundamental physics and chemistry, we must limit our discussion to those areas having direct implications for surface science. [Pg.169]

Marlow and Rowell discuss the deviation from Eq. V-47 when electrostatic and hydrodynamic interactions between the particles must be considered [78]. In a suspension of glass spheres, beyond a volume fraction of 0.018, these interparticle forces cause nonlinearities in Eq. V-47, diminishing the induced potential E. [Pg.188]

At the same level of approximation, the corresponding interaction between two different atoms is [I]... [Pg.229]

Contributions to van der Waals s Interactions between Neutral Molecules... [Pg.230]

The total interaction between two slabs of infinite extent and depth can be obtained by a summation over all atom-atom interactions if pairwise additivity of forces can be assumed. While definitely not exact for a condensed phase, this conventional approach is quite useful for many purposes [1,3]. This summation, expressed as an integral, has been done by de Boer [8] using the simple dispersion formula, Eq. VI-15, and following the nomenclature in Eq. VI-19 ... [Pg.232]

All the long-range forces discussed in this chapter play a role in biological processes. Interactions between membranes, proteins, ligands, antibodies... [Pg.246]

In an extensive SFA study of protein receptor-ligand interactions, Leckband and co-workers [114] showed the importance of electrostatic, dispersion, steric, and hydrophobic forces in mediating the strong streptavidin-biotin interaction. Israelachvili and co-workers [66, 115] have measured the Hamaker constant for the dispersion interaction between phospholipid bilayers and find A = 7.5 1.5 X 10 erg in water. [Pg.247]


See other pages where Interactions between is mentioned: [Pg.9]    [Pg.63]    [Pg.129]    [Pg.114]    [Pg.233]    [Pg.361]    [Pg.369]    [Pg.384]    [Pg.50]    [Pg.142]    [Pg.543]    [Pg.696]    [Pg.698]    [Pg.182]    [Pg.182]    [Pg.202]    [Pg.225]    [Pg.227]    [Pg.233]    [Pg.234]    [Pg.247]    [Pg.247]   


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