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Frequency light

The above fomuilae for the absorption spectrum can be applied, with minor modifications, to other one-photon spectroscopies, for example, emission spectroscopy, photoionization spectroscopy and photodetachment spectroscopy (photoionization of a negative ion). For stimulated emission spectroscopy, the factor of fflj is simply replaced by cOg, the stimulated light frequency however, for spontaneous emission... [Pg.248]

One of the most interesting features of the Raman spectmm is its dependence on tire incident light frequency, coj. When Wj is on resonance with the excited electronic state, the scattering process closely resembles a process of absorption followed by emission. However, as Uj is detuned from resonance there are no longer... [Pg.250]

Altliough an MOT functions as a versatile and robust reaction cell for studying cold collisions, light frequencies must tune close to atomic transitions and an appreciable steady-state fraction of tire atoms remain excited. Excited-state trap-loss collisions and photon-induced repulsion limit achievable densities. [Pg.2471]

Fig. 1. Pumping methods for lasers where is the pump light frequency and is the laser frequency, wavy lines represent radiationless transitions, and the dashed line collisions (a) optical pumping in three-level systems (b) optical pumping in four-level systems (c) pumping by electron impact and... Fig. 1. Pumping methods for lasers where is the pump light frequency and is the laser frequency, wavy lines represent radiationless transitions, and the dashed line collisions (a) optical pumping in three-level systems (b) optical pumping in four-level systems (c) pumping by electron impact and...
The vibrational motions of the chemically bound constituents of matter have fre-quencies in the infrared regime. The oscillations induced by certain vibrational modes provide a means for matter to couple with an impinging beam of infrared electromagnetic radiation and to exchange energy with it when the frequencies are in resonance. In the infrared experiment, the intensity of a beam of infrared radiation is measured before (Iq) and after (7) it interacts with the sample as a function of light frequency, w[. A plot of I/Iq versus frequency is the infrared spectrum. The identities, surrounding environments, and concentrations of the chemical bonds that are present can be determined. [Pg.32]

There are three spectral regions or ranges of light frequencies that are particularly useful to chemists in learning atomic sizes. We shall discuss each briefly. [Pg.248]

Turbidity measurements were determined using the dipping probe colorimeter. The light frequency was 650 nm. Deionized water transmittance was set at 90. The surfactant test solutions were stirred ( — 3500 rpm) and maintained at 75°C. Active surfactant concentration was 0.1% wt. Solution volume was 100 cm1. A 26.5% CaCU (95,699 ppm CaJ+) solution was added via syringe in 0,10 ml increments to the lower portion of the surfactant solution. [Pg.379]

P = arccos(/ J /JJ1), which does not influence the scattered light frequency. The result is... [Pg.99]

Retinal responses to different light frequencies are encoded in the retina and conveyed to the thalamus and visual cortex 808... [Pg.807]

The potential for sunlight (or selected other light frequencies) to transform a drug or product is both a useful tool for activating some drugs and a cause of significant adverse effects for others (such as the quinolone antibiotics [Horio et al., 1995 and... [Pg.389]

If one is interested in spectroscopy involving only the ground Born Oppenheimer surface of the liquid (which would correspond to IR and far-IR spectra), the simplest approximation involves replacing the quantum TCF by its classical counterpart. Thus pp becomes a classical variable, the trace becomes a phase-space integral, and the density operator becomes the phase-space distribution function. For light frequency co with ho > kT, this classical approximation will lead to substantial errors, and so it is important to multiply the result by a quantum correction factor the usual choice for this application is the harmonic quantum correction factor [79 84]. Thus we have... [Pg.63]

Nonlinear optical organic materials such as porphyrins, dyes, and phthalocyanines provide optical limiting properties for photonic devices to control light frequency and intensity in a predictable manner. The optical limit of CNTs composites is saturated at CNTs exceeding 3.8wt% relative to the polymer mass (Chen et al., 2002). Polymer/ CNT composites could also be used to protect human eyes, for example, optical elements, optical sensors, and optical switching (Cao et al., 2002). [Pg.200]

A voltammetric curve can be viewed in electrochemistry as the emission or absorption spectra in spectroscopy. The current density (i.e., the number of charges per unit of time and area) corresponds to the emitted or absorbed light intensity (the number of quanta per unit of time and area). Finally, when multiplied by the Faraday constant, the potential defines the energy of the system and can thus be treated as an analog of the light frequency, which can also gives energy when multiplied by the Planck constant. [Pg.12]

Both the active medium and the resonator determine the light frequencies generated. [Pg.47]

F ure 4.3 The optical magnitudes, n and k, of an ideal metal (undamped free electrons) versus the light frequency. [Pg.123]

For very accurate line profile measurements, a heterodyne technique has been developed 240) which can be briefly explained as follows the light, scattered into a cone within the angle 0 b9 (50< 1 °). is focused onto the cathode of a photomultiplier. The photocurrent is proportional to the square of the incoming light amplitude but cannot follow the rapid light frequency. Any beat frequencies, however, resulting from interference between the... [Pg.49]

At low temperatures and light frequencies, the separative effect per unit shift (the terms in brackets in eq. 11.44 and 11.45) approaches (figure 11.9) and the Helmholtz free energy difference approaches the differences in zero-point energies. At high T (low frequencies), the separative effect per unit shift approaches zero and the total separative effect sis ")/approaches 1, so that no isotopic fractionation is observed. [Pg.729]

Robinson (1967) has used the Unsold approximation for the energy levels to express the polarizabilities in terms of the electrostatic moments of the ground-state electron distribution. The expressions have been applied to X-ray charge densities by Zyss, Baert, and coworkers (Fkyerat et al. 1995 F. Hamzaoui, F. Baert and J. Zyss, private communication). A detailed description of the derivation and the approximations involved is beyond the scope of this treatise. However, it should be mentioned that the severe approximations are made that all excited-state energy levels are equal, and that the exciting light frequency is equal to zero. [Pg.282]

In a typical IRS experiment, the infrared light is separated into its frequencies so that the variation of the absorbed light,13 A, with the light frequency, V, can be monitored. The separation of light into its frequencies is carried out in a spectrometer. [Pg.80]

The value of measurements of the magnitude of the optic axial angle has been urged by Bryant (1932) and where dispersion of the optic axes occurs, the variation of the optic axial angle with light frequency is a highly characteristic feature which is valuable evidence for identity. (See Bryant, 1941, 1943.)... [Pg.105]

With the laser pulse energy W = 10 5 J, the laser spot diameter d = 10X on the dielectric surface, and the light frequency v = 5x 1014 s 1, the electron velocity variation is Au = 2x 108exp(-z/zo) centimeters per second. This means that an electron beam with an energy E - 100 eV (v = 5.9 x 108 cm/s) reflects at a substantial angle of

evanescent wave produced by a femtosecond laser pulse. [Pg.190]

FIGURE 5.8 The photo- electric effect. A plot of the number of electrons ejected from a metal surface versus light frequency shows a threshold value. Increasing the intensity of the light while keeping the frequency the same increases the number of electrons ejected but does not change the threshold value. [Pg.168]

Physically, equation 23 tells us the polarization consists of a second-order DC field contribution to the static polarization (first term), a frequency component w corresponding to the incident light frequency (second term) and a new frequency doubling component, 2co (third term) ( see Figure 15). [Pg.27]


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Frequency Conversion of Laser Light

Frequency Conversion of Light

Frequency of light

Frequency shift, light from moving particle

Frequency-resolved light modulation methods

Light angular frequency

Light pulse frequency spectrum

Light visible frequency

Light, scattering frequency

Light-chopper frequency

Light-emitting diode emission frequencies

Skill 17.7 Relating photon energy to the wavelength and frequency of light

Wave frequency, light

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