Other cases

Other Cases In some cases, a reaction takes place in one of the phases in a multiphase reactor but not in the others. Obviously, it is critical to know the phase in which the reaction occurs. If the definition of the reaction rate is based on the total reactor volume, serious trouble wiU result when the ratio of the phases changes. The ratio of the phases generally will depend on variables such as the reactor dimensions, the intensity of mechanical agitation, and the feed rates and compositions of the various fluids. Therefore, difficulty is inevitable, especially on scaleup, if the reaction rate is misdefined. [Pg.10]

In a few industrial processes, the reaction occurs at the interface between two phases. The inteifacial area then is the appropriate parameter to use in making the reaction rate intensive. The synthesis of poly(bisphenol A carbonate) (polycarbonate) finm bisphenol A and phosgene is an example of a reaction that occurs at the interface between two fluidphases. [Pg.10]

On occasion, a reaction takes place in more than one phase of a multiphase reactor. An example is the so-called catalytic combustion. If the temperature is high enough, a hydrocarbon fuel such as propane can be oxidized catalyticaUy, on the surface of a heterogeneous catalyst, at the same time that a homogeneous oxidation reaction takes place in the gas phase. This situation calls for two separate definitions of the reaction rate, one for the gas phase and the other for the heterogeneous catalyst. [Pg.10]

In addition to the three cases discussed above, in which the building blocks based on functionalized pillararenes and pillararene complexes performed as the amphiphiles, pillararene-based supramolecular networks can also be wrapped into hollow vesicular spheres. For example, pillararene trimer [Pg.219]

Fig ure 9.7 Illustrative mechanism for dual bioimaging by delivering G9.10, FITC, RhB, and DOX from biocompatible pillararene-based [Pg.220]

Reproduced with permission from ref. 26. Copyright 2013 American Chemical Society. [Pg.220]

Adapted from Ref. 7 with permission from The Royal Society of Chemistry. [Pg.222]

Shift and spin patterns for protons and deuterons in solution [Pg.47]

Estimated A/h values (MHz) for H, 13C and l4N nuclei of nitrogen- and sulfur-containing ligands of nickel(II) [Pg.47]

The case of the hexa(pyridine) nickel(II) complex has been extensively debated in the early literature of NMR of paramagnetic complexes [17-21]. The shift pattern with a-H y-H (i-H (Fig. 2.11 and Table 2.3) was soon recognized to be predominantly of a-type. The ligand has a a MO system which has the correct symmetry to overlap with the dx2 y2 and dz2 orbitals. However, spin polarization can induce V2 spin density in the it system. Once some unpaired spin density is in a p orbital, it spin-polarizes the electrons of the C—H a bond, thus producing a further mechanism for transferring spin density on the proton. The proton A/h value from this mechanism is proportional to the spin density on the carbon pz orbital, p , through a proportionality constant ch [Pg.47]

If the spin delocalization mechanism on the pyridine ring were a solely, substitution of y-H with Y-CH3 would produce almost zero spin density on the y-CH3 protons. On the contrary (Table 2.3 and Fig. 2.11), some upheld (negative) shift is observed [22,23]. Spin polarization, from e.g. positive spin density on the pz orbital of an sp2 carbon, produces negative spin density on the attached proton (Fig. 2.12), and positive spin density again on the protons of an attached CH3 moiety (see also Section 2.4). Therefore, if the y-CH3 protons experience upheld [Pg.48]

Patents describe the preparation (by chlorination) of 2,3,5-trichloro-6-cyano-pyrazine (794,795) and the chlorination of 2-methoxy-3-methoxycarbonylpyrazine (product not stated) has been described (155). [Pg.97]

Chlorination of tetrafluoropyrazine has been shown to give 3,6-dichloro-2,2,5,5-tetrafluoro-2,5-dihydropyrazine (2) (50%) and 5,6-dichloro-2,2,33-tetrafluoro-23-dihydropyrazine (3) (10%) (796). [Pg.97]

The absorbed light may act as calalv. i for a spontaneous reaction, but in other cases it may supply energy to make possible a reaction which, without light, would be thermodynamically impossible. In some cases, such a reaction reverses itselfby thermal reaction (e.g. if left in the dark) and, hence, during irradiation a phoiostationary state is reached. [Pg.310]

Inequality Re > H corresponds to the other case, when only a part of a penetrant is extracted by a developer and can form crack s indication. Such a situation can take place when one use kaolin powder as the developer. We measured experimentally the values Rj for some kaolin powders. For the developer s layer of kaolin powder, applied on tested surface. Re = 8 - 20 pm depending on powder s quality. [Pg.614]

In both cases special probes were designed and manufactured For the first ease a special probe which fits geometrically exactly to the contour of the turbine blade and in the other case a combined transducer system was developed which enables a continuous measurement of... [Pg.764]

In wide sectors of industry there is a growing need of inspection methods which go without liquid coupling media. The excitation of bulk and surface waves by means of air-coupled ultrasonic probes is therefore an attractive tool for NDE. This is tme e.g. for the rapid scanning of large composite structures in the aerospace industry [1]. In other cases, the use of liquid couplants is prohibitive like the thickness measurement of powder layers. [Pg.840]

The physical chemist is very interested in kinetics—in the mechanisms of chemical reactions, the rates of adsorption, dissolution or evaporation, and generally, in time as a variable. As may be imagined, there is a wide spectrum of rate phenomena and in the sophistication achieved in dealing wifli them. In some cases changes in area or in amounts of phases are involved, as in rates of evaporation, condensation, dissolution, precipitation, flocculation, and adsorption and desorption. In other cases surface composition is changing as with reaction in monolayers. The field of catalysis is focused largely on the study of surface reaction mechanisms. Thus, throughout this book, the kinetic aspects of interfacial phenomena are discussed in concert with the associated thermodynamic properties. [Pg.2]

Equation XI-27 shows that F can be viewed as related to the difference between the individual adsorption isotherms of components 1 and 2. Figure XI-9 [140] shows the composite isotherms resulting from various combinations of individual ones. Note in particular Fig. XI-9a, which shows that even in the absence of adsorption of component 1, that of component 2 must go through a maximum (due to the N[ factor in Eq. XI-27), and that in all other cases the apparent adsorption of component 2 will be negative in concentrated solution. [Pg.407]

In addition to the case of a metal in contact with its ions in solution there are other cases in which a Galvani potential difference between two phases may be found. One case is the innnersion of an inert electrode, such as platinum metal, into an electrolyte solution containing a substance S that can exist m either an oxidized or reduced fomi tlirough the loss or gain of electrons from the electrode. In the sunplest case, we have... [Pg.598]

Although this discussion has been in temis of molecules in solution, the same principles apply to other cases, such as precipitates in an alloy or composites of ceramic particles dispersed in a polymer. The density, p(r), is... [Pg.1370]

For a more complete understanding of colloid stability, we need to address the kinetics of aggregation. The theory discussed here was developed to describe coagulation of charged colloids, but it does apply to other cases as well. First, we consider the case of so-called rapid coagulation, which means that two particles will aggregate as soon as they meet (at high salt concentration, for instance). This was considered by von Smoluchowski 1561 here we follow [39, 57]. [Pg.2683]

Consider again the prototypical homogeneous reaction (C2.14.13), which Renyi has analysed in detail 1801. Taking the forward reaction only (other cases are also dealt with in [80]), and supposing that kj. 4 n (d +dj )(Dg+Dj (cf equation (C2.14.20)), then... [Pg.2829]

In other cases, the zeroth-order vibronic levels are generally more than twofold degenerate and the perturbative handling is much more complicated. An exception is the case 07= , U( =li K = 0 with the twofold degenerate zeroth-order level. The basis functions are 1 1 1 1 —) = 1) and 1 —1 1 —l- -)s 2). The zeroth-order energy is... [Pg.544]

The chloride is white, the bromide pale yellow and the iodide deeper yellow. These are examples (uncommon) of a coloured compound being obtained from colourless ions. The silver(I) ion intensifies colour in other cases, for example silver chromate(VI), Ag2Cr04, is brick-red while potassium chromaie(VI). K2Cr04. is yellow. [Pg.427]

During the process of conversion, a program may drop some information produced by other software because the format conventions cannot handle this additional information. For example, when the J ACMP format is converted to a Molfile, its content is reduced to structural data only, without spectra data. In other cases, a... [Pg.46]

Specialty search engines are to be preferred if a database or a detailed menu is available in any other case make use of their directory scan more than one to three result pages. The relevance ranking of a search engine may not correspond to yottr preferences. [Pg.276]

The input to a minimisation program consists of a set of initial coordinates for the system. The initial coordinates may come from a variety of sources. They may be obtained from an experimental technique, such as X-ray crystallography or NMR. In other cases a theoretical method is employed, such as a conformational search algorithm. A combination of experimenfal and theoretical approaches may also be used. For example, to study the behaviour of a protein in water one may take an X-ray structure of the protein and immerse it in a solvent bath, where the coordinates of the solvent molecules have been obtained from a Monte Carlo or molecular dynamics simulation. [Pg.275]

Semiempirical calculations tend to be qualitative. In some cases, the correct trends have been predicted. In other cases, semiempirical methods give incorrect signs as well as unreasonable magnitudes. [Pg.259]

One of the major selling points of Q-Chem is its use of a continuous fast multipole method (CFMM) for linear scaling DFT calculations. Our tests comparing Gaussian FMM and Q-Chem CFMM indicated some calculations where Gaussian used less CPU time by as much as 6% and other cases where Q-Chem ran faster by as much as 43%. Q-Chem also required more memory to run. Both direct and semidirect integral evaluation routines are available in Q-Chem. [Pg.340]

In all other cases the observed result will depend upon both the speed of mixing and the speed of nitration. The relative rate will be greater than unity by an amount peculiar to the conditions of the experiment. Again, if the alkylbenzene is sufficiently reactive to be nitrated upon encounter, whilst benzene is not, the relative rate will be greater than unity and, for the experimental conditions, will be a limiting upper value no matter what aromatic is used. [Pg.65]

It has been necessary to comment upon these various studies because Olah and his co-workers have suggested that whilst nitrations, like those with nitronium salts, which give a relative rate of reaction of toluene with respect to benzene not much greater than unity involve the nitronium ion as the electrophile, this is not so in other cases. It is important to consider these opinions closely. In the earlier of the two relevant papers it is agreed that since nitrations of toluene with nitronium tetrafluoroborate in sulpholan show no abnormal o -ratio there... [Pg.70]

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