Static reactivity

Bonaccorsi ct al. [204 defined for the first time the molecular electrostatic potential (MEP), wdicli is dearly tfie most important and most used property (Figure 2-125c. The clcctro.static potential helps to identify molecular regions that arc significant for the reactivity of compounds. Furthermore, the MEP is decisive for the formation of protein-ligand complexes. Detailed information is given in Ref [205]. 

ANSI/lEEE-519/1993 Guide for harmonic control and reactive compensation of static power converters ... 

Although costlier, when a smoother and faster p.f. correction is desirable, without causing an overvoltage or inflow current, static switchings should be chosen. They have most application in large automatic reactive power controls, as discussed in Section 24.10. 

In SVCs Ihe number of switchings is of no relevance, as they arc free from inrush currents. Switching is performed at the instant when the cuiTcnt wave is passing through its natural zero. Static devices in various combinations and feedback control systems, which may be computer-aided, can tilmost instantaneously (< I cycle) generate or absorb reactive power, as may be demanded by the system. Correction... 

This part considers reactive power control with the use of shunt and series capacitors. The controls may be manual or automatic through electromagnetic or static devices. Protection of capacitors and capacitor banks as well as design, manufacturing and test requirements, installation and maintenance are also covered, the main thrust being on the application of power capacitors. 

We can distinguish between static theories, which in essence give a description of the electron density, and dynamic theories, where an attempt is marie to measure the response of a molecule to (e.g.) an approaching N02" " ion. In recent years, the electrostatic potential has been used to give a simple representation of the more important features of molecular reactivity. It can be calculated quite easily at points in space ... 

The excitation system provides the magnetizing current necessary for the generator to operate at the desired voltage and, when in parallel with other generators, supplies the required amount of reactive current. In modern practice the excitation system can be either brushless or static. 

Reaction turbine design also makes use of steam jets (which are produced by steam flowing across static vanes), although the turbine has rotor discs that incorporate movable blades rather than buckets. The design utilizes the reactive force produced by steam accelerating through a nozzle (created by the combination of a stationary vane and a moving blade) to rotate the shaft. 

Barrett and Thomas (10)proposed that these effects of differential monomer adsorption could be modeled by correcting homogeneous solution copolymerization reactivity ratios with the monomer s partition coefficient between the particles and the diluent. The partition coefficient is measured by static equilibrium experiments. Barrett s suggested equations are ... 

Chemical reactions in boundary lubrication are different from static reactions even if the reactive substances involved are the same. The temperature to activate a chemical reaction on rubbing surfaces is usually lower than that required in the static chemical process. Some believe this is because of the naked surfaces and structural defects created by the friction/wear process, which are chemically more active. Kajdas proposed a new concept that accumulations of stress and strain in friction contacts could cause emission of low-... 

Elucidation of degradation kinetics for the reactive extrusion of polypropylene is constrained by the lack of kinetic data at times less than the minimum residence time in the extruder. The objectives of this work were to develop an experimental technique which could provide samples for short reaction times and to further develop a previously published kinetic model. Two experimental methods were examined the classical "ampoule technique" used for polymerization kinetics and a new method based upon reaction in a static mixer attached to a single screw extruder. The "ampoule technique was found to have too many practical limitations. The "static mixer method" also has some difficult aspects but did provide samples at a reaction time of 18.6 s and is potentially capable of supplying samples at lower times with high reproducibility. Kinetic model improvements were implemented to remove an artificial high molecular weight tail which appeared at high initiator concentrations and to reduce step size sensitivity. 

Carbon monoxide chemisorption was used to estimate the surface area of metallic iron after reduction. The quantity of CO chemisorbed was determined [6J by taking the difference between the volumes adsorbed in two isotherms at 195 K where there had been an intervening evacuation for at least 30 min to remove the physical adsorption. Whilst aware of its arbitrariness, we have followed earlier workers [6,10,11] in assuming a stoichiometry of Fe CO = 2.1 to estimate and compare the surface areas of metallic iron in our catalysts. As a second index for this comparison we used reactive N2O adsorption, N20(g) N2(g) + O(ads), the method widely applied for supported copper [12]. However, in view of the greater reactivity of iron, measurements were made at ambient temperature and p = 20 Torr, using a static system. 

From 1933 85>, several theoretical approaches to the problem of the chemical reactivity of planar conjugated molecules began to appear, mainly by the Huckel molecular orbital theory. These were roughly divided into two groups 36>. The one was called the "static approach 35,37-40)j and the other, the "localization approach 41,42). in 1952, another method which was referred to as the "frontier-electron method was proposed 43> and was conventionally grouped 44> together with other related methods 45 48> as the "delocalization approach". 

Thus, the local (static) quantities represent the stationary properties affecting the static pressure and the local reactivity in a nuclear reactor. The flow (dynamic) quantities represent the transport properties affecting the energy, momentum, and mass balances of a flow. 

Contents Structure and reactivity of monomeric, molecular tin(ll) compounds / M. Veith, O. Recktenwald — Chirality, static and dynamic stereochemistry of organotin compounds / M. Gielen — Coordination effects in formation and cross-linking reactions of organotin macromolecules / Z. M. O. Rzaev. 1. Organotin compounds — Addresses, essays, lectures. I. Gielen, M. (Marcel), 1938 — II. Series. 

Although the massive metal is relatively inert, when powdered it becomes very reactive. The dry powder may react explosively at elevated temperatures with nitrogen, phosphorus, oxygen, sulfur and other non-metals. The halogens react similarly, and in contact with hot cone, nitric acid and other oxidants it may explode (often after a delay with nitric acid). The powder is pyrophoric and readily ignitable by friction, heat or static sparks, and if dry bums fiercely. Presence of... 

The general reactivity of the sulfide depends markedly on the physical form, and differences of a factor of 10 may be involved. It is ignitable by friction, sparks or flames, and ignites in dry air if heated close to the m.p., 275 -280°C. The dust (200 mesh) forms explosive mixtures in air above a concentration of 0.5% w/v [1], and maximum explosion pressures of 4.35 bar, with maximum rate of rise exceeding 680 bar/s have been determined [2], The dust can acquire sufficient static electricity from movement for ignition to occur [3],... 

Sonochemistry is strongly affected by a variety of external parameters, including acoustic frequency, acoustic intensity, bulk temperature, static pressure, choice of ambient gas, and choice of solvent. These are important considerations in the effective use of ultrasound to influence chemical reactivity, and are also easily understandable in terms of the cavitational hot-spot mechanism. A summary of these effects is given in Table II. 

The independent reaction time (1RT) model was introduced as a shortcut Monte Carlo simulation of pairwise reaction times without explicit reference to diffusive trajectories (Clifford et al, 1982b). At first, the initial positions of the reactive species (any number and kind) are simulated by convolving from a given (usually gaussian) distribution using random numbers. These are examined for immediate reaction—that is, whether any interparticle separation is within the respective reaction radius. If so, such particles are removed and the reactions are recorded as static reactions. 

A vital activity of the chemical sciences is the determination of structure. Detailed molecular structure determinations require identifying the spatial locations of all of the atoms in molecules, that is, the atomic distances and bond angles of a species. It is important to realize that the three-dimensional architecture of molecules very much defines their reactivity and function. However, molecules are dynamic, a feature that is not reflected by static pictures. This last point requires further explanation. Because the atoms in all molecules move, even in the limit of the lowest temperatures obtainable, molecular structures really describe the average position about some equilibrium arrangement. In addition, rotations about certain bonds occur freely at common temperatures. Consequently, some molecules exist in more than one structure (conformation). Some molecules are so floppy that structural characterizations really refer to averages among several structures. Yet other molecules are sufficiently rigid that molecular structures can be quite precisely determined. 

Pseudomonas luteola Reactive azo dyes, Direct azo dyes and leather dyes The 59-99% color removal after 2-6 days static incubation, at dye concentration of 100 mg L 1, monoazo dyes showing fastest rate of decoloration [78]... 

Pseudomonas luteola Reactive red 22 Flask Sequential batch Static and agitated incubation E Ca arginate, k carageenan polyacryl. gel 0-200 20-47 5-10... 

Pseudomonas luteola Reactive red 22 Flask Batch Static incubation F - 0-400 20-47 5-9... 

Introduction of the static density response function for a system with a constant number of electrons yields the RF - DFT model. This second approach is expected to be more useful in the analysis of chemical reactivity in condensed phases. 

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