Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Other Processes of Interest

Crystal nucleation from the melt is but one type of nucleation in the condensed phase. Other processes of interest include the nucleation of salt crystals from aqueous solution, of one crystalline phase from another or from a glass, and of liquid crystal phases from one another or from the isotropic liquid. In this review we discuss only the nucleation of crystals from the melt. The major emphasis will be on single-component systems, although crystallization of alloys and binary mixtures will also be considered. [Pg.264]

The biodistribution of the ideal radiopharmaceutical would show extremely rapid distribution via the circulatory system to the organs of interest and htfle distribution to others. It would be rapidly extracted by the organ or tissue of interest differentially in a way that reflects the disease process of interest. Ideally, abnormahties should be defined by substantial increases in the concentration of the agent because lesions defined by a decrease from surrounding concentrations, ie, cold-spot imaging, are more difficult to image. [Pg.473]

To solve a flow problem or characterize a given fluid, an instmment must be carefully selected. Many commercial viscometers are available with a variety of geometries for wide viscosity ranges and shear rates (10,21,49). Rarely is it necessary to constmct an instmment. However, in choosing a commercial viscometer a number of criteria must be considered. Of great importance is the nature of the material to be tested, its viscosity, its elasticity, the temperature dependence of its viscosity, and other variables. The degree of accuracy and precision required, and whether the measurements are for quaUty control or research, must be considered. The viscometer must be matched to the materials and processes of interest otherwise, the results may be misleading. [Pg.178]

Cheletropic processes are defined as reactions in which two bonds are broken at a single atom. Concerted cheletropic reactions are subject to orbital symmetry analysis in the same way as cycloadditions and sigmatropic processes. In the elimination processes of interest here, the atom X is normally bound to other atoms in such a way that elimination gives rise to a stable molecule. In particular, elimination of S02, N2, or CO from five-membered 3,4-unsaturated rings can be a facile process. [Pg.591]

Table 4.3 shows the feed of each component and the total flow to each unit. The composition of any other stream of interest can be calculated from these values and the split-fraction coefficients. The compositions and flows should be checked for compliance with the process constraints, the split-fraction values adjusted, and the calculation repeated, as necessary, until a satisfactory fit is obtained. Some of the constraints to check in this example are discussed below. [Pg.183]

Although the basic mechanisms are generally agreed on, the difficult part of the model development is to provide the model with the rate constants, physical properties and other model parameters needed for computation. For copolymerizations, there is only meager data available, particularly for cross-termination rate constants and Trommsdorff effects. In the development of our computer model, the considerable data available on relative homopolymerization rates of various monomers, relative propagation rates in copolymerization, and decomposition rates of many initiators were used. They were combined with various assumptions regarding Trommsdorff effects, cross termination constants and initiator efficiencies, to come up with a computer model flexible enough to treat quantitatively the polymerization processes of interest to us. [Pg.172]

Although current processing temperatures for A1PO dielectrics remain above the threshold for plastic substrates, they are well within the thermal budget of several other substrates of interest for large-area applications. [Pg.124]

The nickel-catalyzed [4 + 4]-cycloaddition of butadiene to form cyclooctadiene was first reported by Reed in 1954.90 Pioneering mechanistic and synthetic studies largely derived from the Wilke group advanced this process to an industrially important route to cyclodimers, trimers, and other molecules of interest.91-94,943 95,96 While successful with simple dienes, this process is not useful thus far with substitutionally complex dienes as needed in complex molecule synthesis. In 1986, Wender and Ihle reported the first intramolecular nickel-catalyzed [4 + 4]-reaction of... [Pg.618]

The substitution reaction of CP with methyl chloride, 2-chloroethyl radical, and allyl chloride has been treated by several different ab initio theoretical models. Depending on the method, the intrinsic barrier for the 5ivr2 process in allyl chloride is 7-11 kcalmoP higher than the barrier for the 5ivr2 reaction of methyl chloride. The reaction of CP with the 2-chloroethyl radical involves an intermediate complex, which is best described as an ethylene fragment flanked by a resonating chloride anion-chloride radical pair. There are many other points of interest. [Pg.325]

The development of the electrodynamic balance and other particle traps has made it possible to perform precise measurements of the properties of small particles by focusing on the single particle. The variety of processes and phenomena that can be investigated with particle traps is quite extensive and includes gas/liquid and gas/solid chemical reactions, chemical spectroscopies, heat and mass transfer processes, interfacial phenomena, thermodynamic properties, phoretic forces, and other topics of interest to chemical engineers. [Pg.3]

The vapor pressures at 1473 K of a few of the actinide elements and other materials of interest are given in Table III. All of the actinide (An) elements through einsteinium can be obtained by this process ... [Pg.5]

In the elimination processes of interest here, the atom X is normally bound to other atoms in such a way that elimination will give rise to a stable molecule. The most common examples involve five-membered rings. [Pg.403]

This topic is well covered by the contributions in this volume. CMP continues to be viewed as a surprisingly unique and flexible semiconductor fabrication technology by virtue of its ability to make manufactureable potential fabrication sequences that are either too cumbersome or too low in yield to be fabricated in any other manner. Using virtually any CMP polisher, a variety of materials of interest to IC fabricators can be planarized. These materials include insulators, semiconductors, interconnect metals, and barrier metallurgies. This means that once a user becomes adept in polishing one kind of material, typically oxide and W at first, other materials of interest and other semiconductor processing sequences become viable. [Pg.3]

Besides the spin-forbidden processes of Sections VII-XII, there are a number of other spin-forbidden processes of interest. Intersystem crossing may occur in certain predissociation phenomena and in P-type delayed fluorescence.198 Also of interest are the heavy atom effect and the direct interaction of radiation with spin. [Pg.48]

In this chapter, Section 10.2 gives an overview of the operation of the Argonne centrifugal contactor. Section 10.3 focuses on the design principles for this contactor. Section 10.4 discusses the worldwide applications of this contactor to solvent-extraction processes of interest to the nuclear and other industries. Comparisons with other types of contactors are made throughout the text, and a separate section is devoted to them in Section 10.4. However, because of their widespread use and the author s particular experience with them, the ANL contactor and its variations remain the primary focus. [Pg.565]


See other pages where Other Processes of Interest is mentioned: [Pg.180]    [Pg.187]    [Pg.116]    [Pg.30]    [Pg.277]    [Pg.26]    [Pg.180]    [Pg.187]    [Pg.116]    [Pg.30]    [Pg.277]    [Pg.26]    [Pg.125]    [Pg.91]    [Pg.169]    [Pg.362]    [Pg.322]    [Pg.387]    [Pg.137]    [Pg.142]    [Pg.92]    [Pg.253]    [Pg.178]    [Pg.194]    [Pg.9]    [Pg.302]    [Pg.125]    [Pg.25]    [Pg.19]    [Pg.98]    [Pg.309]    [Pg.222]    [Pg.288]    [Pg.116]    [Pg.143]    [Pg.340]    [Pg.125]    [Pg.483]    [Pg.103]    [Pg.70]   


SEARCH



Other processes

© 2024 chempedia.info