Big Chemical Encyclopedia

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

Articles Figures Tables About

Variable Retarders

Fig. 6. Potential distribution and electron kinetic energy functions in a simple ion source using the R.P.D. method (see text) the effect of a variable retarding potential is shown schematically. Fig. 6. Potential distribution and electron kinetic energy functions in a simple ion source using the R.P.D. method (see text) the effect of a variable retarding potential is shown schematically.
Variable retardation can also be achieved using electric birefringence induced in liquid layers. Commercial devices are available that use this method. [Pg.189]

The neutral beam is pulsed by a rotating chopper wheel (E) at a frequency of about 200 Hz to discriminate the product ions formed in the reaction zone from those produced outside the reaction zone. The source is operated at 55°C and is assumed to provide a corresponding Boltzmann distribution. The energy analyser (F) consists of a fine grid (90 lines per in.) at the potential of the last ion lens, followed by a finer screen (375 lines per in.) to which variable retarding potential is applied. [Pg.331]

The electron energy selection is usually made through two different modes fixed analyzer transmission and fixed retardation ratio. The first one is the one used when a quantitative analysis is required. It consists of keeping the analyzer voltages constant, the kinetic energy being swept by a variable retardation voltage... [Pg.285]

Commercially available compensators with variable retardation are of the following types. [Pg.69]

Cblorina.ted Pa.ra.ffins, The term chlotinated paraffins covers a variety of compositions. The prime variables are molecular weight of the starting paraffin and the chlorine content of the final product. Typical products contain from 12—24 carbons and from 40—70 wt % chlorine. Liquid chlotinated paraffins are used as plasticizers (qv) and flame retardants ia paint (qv) and PVC formulations. The soHd materials are used as additive flame retardants ia a variety of thermoplastics. In this use, they are combiaed with antimony oxide which acts as a synergist. Thermal stabilizers, such as those used ia PVC (see vinyl polymers), must be used to overcome the inherent thermal iastabiUty. [Pg.469]

Laboratory experiments using rodents, or the use of gas analysis, tend to be confused by the dominant variable of fuel—air ratio as well as important effects of burning configuration, heat input, equipment design, and toxicity criteria used, ie, death vs incapacitation, time to death, lethal concentration, etc (154,155). Some comparisons of polyurethane foam combustion toxicity with and without phosphoms flame retardants show no consistent positive or negative effect. Moreover, data from small-scale tests have doubtful relevance to real fine ha2ards. [Pg.481]

In an electrooptic material the phase retardation angle is controlled by altering birefringence, which is in turn controlled by the potential of an apphed electric field. An electrooptic device thus acts as a variable phase optical retardation plate, and can be used to modulate the wavelength or intensity of an incident beam. [Pg.340]

There are methods to manipulate the backbones of polymers in several areas that include control of microstructures such as crystallinity, precise control of molecular weight, copolymerization of additives (flame retardants), antioxidants, stabilizers, etc.), and direct attachment of pigments. A major development with all this type action has been to provide significant reduction in the variability of plastic performances, more processes can run at room temperature and atmospheric pressure, and 80% energy cost reductions. [Pg.373]

The retarding influence of the product barrier in many solid—solid interactions is a rate-controlling factor that is not usually apparent in the decompositions of single solids. However, even where diffusion control operates, this is often in addition to, and in conjunction with, geometric factors (i.e. changes in reaction interfacial area with a) and kinetic equations based on contributions from both sources are discussed in Chap. 3, Sect. 3.3. As in the decompositions of single solids, reaction rate coefficients (and the shapes of a—time curves) for solid + solid reactions are sensitive to sizes, shapes and, here, also on the relative dispositions of the components of the reactant mixture. Inevitably as the number of different crystalline components present initially is increased, the number of variables requiring specification to define the reactant completely rises the parameters concerned are mentioned in Table 17. [Pg.249]

It is possible to determine components in complex EPs where matrix effects can be severe. For example, zinc (as zinc borate), chlorine (as dechlorane flame retardant), antimony (as oxide) and fibre-glass have been determined in nylon using just one standard. Many users have refined the universal precalibrated programmes for standardless XRF and made them more efficient for matrix correction by using variable correction coefficients. OilQuant offers possibilities for analysing polymers [243]. Software packages usually provide ... [Pg.633]

Often these design criteria involve competitive requirements. What is best for meeting one criterion may be counterproductive in meeting another. For example, certain excipients such as the hydrophobic stearate lubricants are important for efficient manufacture, yet they have the potential to retard the release of drug from an immediate-release formulation. The design of a dosage form thus frequently requires the optimization of formulation and process variables in a way that best meets all design criteria. [Pg.362]


See other pages where Variable Retarders is mentioned: [Pg.418]    [Pg.160]    [Pg.189]    [Pg.189]    [Pg.26]    [Pg.39]    [Pg.47]    [Pg.218]    [Pg.36]    [Pg.480]    [Pg.214]    [Pg.305]    [Pg.75]    [Pg.160]    [Pg.493]    [Pg.31]    [Pg.418]    [Pg.160]    [Pg.189]    [Pg.189]    [Pg.26]    [Pg.39]    [Pg.47]    [Pg.218]    [Pg.36]    [Pg.480]    [Pg.214]    [Pg.305]    [Pg.75]    [Pg.160]    [Pg.493]    [Pg.31]    [Pg.419]    [Pg.337]    [Pg.340]    [Pg.110]    [Pg.522]    [Pg.327]    [Pg.261]    [Pg.108]    [Pg.211]    [Pg.31]    [Pg.4]    [Pg.142]    [Pg.607]    [Pg.76]    [Pg.141]    [Pg.361]    [Pg.423]    [Pg.208]    [Pg.119]   


SEARCH



Retardation variable

Retardation variable

Variable retardation plates

© 2024 chempedia.info