Electrostatic , generally accelerators

Fig. 2.9. General schematic of a sector mass analyzer. Ions extracted from the ion source are accelerated by an electrostatic field (accelerating potential, 10 and enter the sector analyzer with velocity, v. Electric (electric flux density, E) or magnetic (magnetic flux density, 6) fields bend the trajectory of the ions into curved paths with radius, r. Trajectories of ions with larger m/z are affected more than smaller ones. An illustration of the direction-focusing ion beam approach in a magnetic sector mass analyzer is shown in the insert. Due to the dependence of the radius of an ion s trajectory on its kinetic energy ( ) in the electrostatic sector mass analyzer and on its momentum (mv) in the magnetic sector mass analyzer, the systems are also referred to as ion energy and ion momentum filters.

Rotary atomisation produces the most uniform atomisation of any of the aforementioned techniques, and produces the smallest maximum particle sise. It is almost always used with electrostatics and at lower rotational speeds the electrostatics assist the atomisation. At higher rotational speeds the atomisation is principally mechanical in nature and does not depend on the electrical properties of the coating material. If the viscosity of a coating material is sufficiendy low that it can be deUvered to a rotary atomiser, the material can generally be atomised. The prime mover is usually an ak-driven turbine and, provided that the turbine has the requked power to accelerate the material to the angular velocity, Hquid-dow rates of up to 1000 cm /min can be atomised using an 8-cm diameter beU. 

On the basis of the above, the rate acceleration afforded by lysozyme appears to be due to (a) general acid catalysis by Glu (b) distortion of the sugar ring at the D site, which may stabilize the carbonium ion and the transition state) and (c) electrostatic stabilization of the carbonium ion by nearby Asp. The overall for lysozyme is about 0.5/sec, which is quite slow (Table... 

MICELLAR CATALYSIS. Chemical reactions can be accelerated by concentrating reactants on a micelle surface or by creating a favorable interfacial electrostatic environment that increases reactivity. This phenomenon is generally referred to as micellar catalysis. As pointed out by Bunton, the term micellar catalysis is used loosely because enhancement of reactivity may actually result from a change in the equilibrium constant for a reversible reaction. Because catalysis is strictly viewed as an enhancement of rate without change in a reaction s thermodynamic parameters, one must exercise special care to distinguish between kinetic and equilibrium effects. This is particularly warranted when there is evidence of differential interactions of substrate and product with the micelle. Micelles composed of optically active detergent molecules can also display stereochemical action on substrates. ... 

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