Übersetzung für "Vapor density" in Deutsch

Furthermore, it is known that the vapor density decreases during smoking.

The gases required for reactive vapor deposition to be reacted with the vaporized substance are supplied to the position of highest vapor density in front of the anode.

The vapor density in the chamber 3 adjusts automatically depending on the electrical energy drawn and the heat flow resulting therefrom.

Due to the presence of a preselected low-pressure gas filling, the electrode erosion is significantly reduced, since the gas filling replaces a significant part of the vapor density necessary for current transport.

The density, vapor pressures and other relevant properties of the formulations were measured, according to which just 22% to 39% of the generated aerosol particles have an aerodynamic diameter of less than or equal to 11.2 ?m.

In this manner of control it is taken into account that a vapor having high density and high pressure, which leads to a correspondingly high pressure on the suction side of the compressor, is present in the evaporator after an extended stoppage of a refrigerating system because of the comparatively high evaporator temperature which is then present and which can possibly correspond to the ambient temperature.

If the refrigerating system is now put into operation the motor which drives the compressor must perform considerable compression work because the compression of high-density vapor requires substantially greater output than the compression of vapors with lower density.

Due to the high vapor density and the liquid film as a result of condensation, the complete heating-up process takes place at an oxygen free environment.

Moreover, the reliable and accurate guided wave radar technology offers a versatile solution that is virtually unaffected by process conditions such as temperature, pressure, vapor gas mixtures, density, turbulence, bubbling/boiling, varying dielectric media, pH, and viscosity.

The effect achieved by the special arrangement of the open-pored, absorbent body in the immediate vicinity of the vapor formation zone—i.e. in a region of high vapor density—is that the condensate residues are absorbed in a very high concentration and therefore highly effectively, and said condensate residues cannot offer the opportunity at all of dispersing into peripheral regions.

It is particularly favorable if the open-pored, absorbent body directly covers the wick capillary structure which is exposed in said section, since the greatest vapor density should be anticipated in this zone.

The mixture as claimed in claim 1, in which physical properties selected from density, vapor pressure, viscosity, heat capacity and thermal conductivity of the mixture, after attainment of a constant temperature between 300° C. and 600° C. under exclusion of air, change by not more than 15% before attainment of an equilibrium composition.

The degree to which the physical properties selected from density, vapor pressure, viscosity, heat capacity and thermal conductivity of the siloxanes of general formula I change in operation, more particularly the degree to which all these properties change in the course of the intended use, amounts to not more than 15%, preferably to not more than 10% and more preferably to not more than 5%.

The composition of the mixture is selected such that at least one of the physical properties of density, vapor pressure, viscosity, heat capacity or thermal conductivity remains nearly constant over time at a constant temperature during thermal stress on the mixture.

The inventive siloxane mixtures have the advantage that at least one physical property selected from density, vapor pressure, viscosity, heat capacity and thermal conductivity can be kept constant over time, even though the chemical composition of the siloxane mixture is still changing until attainment of the equilibrium state.

Preferably, the physical properties, selected from density, vapor pressure, viscosity, heat capacity and thermal conductivity of the mixture, especially all these properties, after attainment of a constant temperature between 300° C. and 600° C. under exclusion of air, change by not more than 15%, preferably not more than 10%, more preferably not more than 5%, before attainment of the equilibrium composition.

The BfR assumes that as vapor density drops down the quantity of substances that are transported and inhaled decreases as well.

The annual average temperature is calculated from deviations of water deuterium concentrations (heavy water DHO has a different dependence of vapor density on condensation temperature compared with H 2 O).

There are indications that the vapor density varies on a case-by-case basis not only for different e-cigarette models but even for identical models.

The Soave-Redlich-Kwong equation of state describes the vapor densities of pure components and mixtures quite well but the deviations of the liquid density prediction are high.

Each of these film samples was then exposed to the light of a high-pressure mercury vapor lamp in a commercial continuous diazo film duplicator under a silver gray wedge which had optical density increments of about 0.15, in such a manner that, after development with moist ammonia vapors, an optical density was obtained under the first exposure step of the silver gray wedge which was by 0.02 density units higher than the density of the completely exposed and developed background of the film sample.

On the other hand, the maintenance-free service life of the ion sources does not correspond to the requirements of industrial application because of the high vapor densities and the attendant high soiling rates.