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Photon pressure potential

Fig. 1. Rates of CO2 assimilation, A (/miol s ) leaf conductance, g (mol m s ) intercellular partial pressure of CO2, Pi (Pa) soil water potential and leaf water potential, xp (MPa) during gas-exchange measurements of a 30-day-old cotton plant, plotted against day after watering was withheld. Measurements were made with 2 mmol m sec" photon flux density, 30 °C leaf temperature, and 2.0 kPa vapour pressure difference between leaf and air (S.C. Wong, unpublished data). Fig. 1. Rates of CO2 assimilation, A (/miol s ) leaf conductance, g (mol m s ) intercellular partial pressure of CO2, Pi (Pa) soil water potential and leaf water potential, xp (MPa) during gas-exchange measurements of a 30-day-old cotton plant, plotted against day after watering was withheld. Measurements were made with 2 mmol m sec" photon flux density, 30 °C leaf temperature, and 2.0 kPa vapour pressure difference between leaf and air (S.C. Wong, unpublished data).
Fig. 2. Rates of CO2 assimilation,. 4, and leaf conductances, g, as functions of intercellular partial pressure of CO2, p in Zea mays on various days after withholding watering. Measurements made with 9.5,19.0,30.5, and 38.0 Pa ambient partial pressure of CO2, 2 mmol m" s" photon flux density, 30 °C leaf temperature, and 2.0 kPa vapour pressure differences between leaf and air. Closed symbols represent measurements with 30.5 Pa ambient partial pressure of COj. Leaf water potentials were 0.05, - 0.2, - 0.5 and - 0.8 MPa on day 0, 4, 11 and 14, respectively (after Wong et al., 1985). Fig. 2. Rates of CO2 assimilation,. 4, and leaf conductances, g, as functions of intercellular partial pressure of CO2, p in Zea mays on various days after withholding watering. Measurements made with 9.5,19.0,30.5, and 38.0 Pa ambient partial pressure of CO2, 2 mmol m" s" photon flux density, 30 °C leaf temperature, and 2.0 kPa vapour pressure differences between leaf and air. Closed symbols represent measurements with 30.5 Pa ambient partial pressure of COj. Leaf water potentials were 0.05, - 0.2, - 0.5 and - 0.8 MPa on day 0, 4, 11 and 14, respectively (after Wong et al., 1985).
According to Eq. (20), we measure only q, q, and the pressure of a gas in the chamber to obtain the absolute values of the photoabsorption cross sections (cr), and then we obtain the values of from a following Eq. (18) or Eq. (19). If we use a rare gas as reference, of which is unity in the whole range above its first ionization potential, then /q is obtained. Thus the relation between Iq and the signal from the incident photon detector,... [Pg.111]

Figure 4. (a) Potential-energy diagram for HI, with arrows showing the one- and three-photon paths whose interference is used to control the ratio of products formed in the branching reactions HI - I+ + e and HI H + I. (b) Modulation of the HI+ and I+ signals as a function of phase difference between the one- and three-photon pathways (proportional to the H2 pressure in the cell used to phase shift the beams). (From Ref. 15.)... [Pg.225]

But any complete description of the evolution of perturbations in the universe will link all of these terms initial velocity and density perturbations to the various components (baryons, dark matter, photons) evolve prior to last scattering as discussed above, and so photon overdensities occur in potential wells, and velocity perturbations occur in response to gravitational and pressure forces. Indeed, to solve this problem in its most general form, we must resort to the Boltzmann equation. The Boltzmann equation gives the evolution of the distribution function, fi(xp,Pp) for a particle of species i with position Xp, and momentum p/(. In its most general form, the Boltzmann equation is formally... [Pg.184]

The APPI source is one of the last arrivals of atmospheric pressure sources [80,81]. The principle is to use photons to ionize gas-phase molecules. The scheme of an APPI source is shown in Figure 1.34. The sample in solution is vaporized by a heated nebulizer similar to the one used in APCI. After vaporization, the analyte interacts with photons emitted by a discharge lamp. These photons induce a series of gas-phase reactions that lead to the ionization of the sample molecules. The APPI source is thus a modified APCI source. The main difference is the use of a discharge lamp emitting photons rather than the corona discharge needle emitting electrons. Several APPI sources have been developed since 2005 and are commercially available. The interest in the photoionization is that it has the potential to ionize compounds that are not ionizable by APCI and ESI, and in particular, compounds that are non-polar. [Pg.56]


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Pressure potential

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