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Total beam collimation

Broadening of the reflected beam does not appreciably worsen resolution if the total beam width remains comparable with the collimator aperture. Such broadening is certainly permissible if it is accompanied by a desirable increase in total reflected intensity. If broadening appreciably exceeds this limit, lines thought to be fully resolved may actually... [Pg.115]

A small fraction of the pump beam generates a broad spectral continuum in a sapphire plate. The larger fraction is frequency doubled and sent by beam splitters into three BBO crystals for parametric amplification. The seed beam collimated from the focal spot in the sapphire plate is also imaged into the three BBO crystals, where they are superimposed on the frequency-doubled pump beams. The three parametric amplifiers can be independently tuned by changing the orientations of the crystals. The total tuning range is only limited by the spectral bandwidth of the seed beam continuum. [Pg.312]

We say then that a crystal is satisfactory for purposes of chemical analysis if the beam it reflects is monochromatic within the limits established by the collimating system. As theory shows,15 some broadening is to be expected on Bragg reflection even from perfect crystals, but this broadening is so small (not over 0.001°) that we need not consider it. Relatively few crystals, notably some diamonds and calcites, approach perfection. Sodium chloride, more useful in x-ray spectrog-raphy, broadens monochromatic x-rays appreciably, but the. total broadening can be smaller than 0.30°,16 the collimator a perture. See Figure 4-9. [Pg.115]

Typically, a source gas such as boron trifluoride [7637-07-2], BF3, is exposed to an ion source that causes the gas to ionize. An analyzer discriminates between all the ionic particles using a magnetic field that can select particles having the correct mass-to-charge ratio to pass through the analyzer to an acceleration tube. The ions are accelerated in the tube and collimated into a beam that is scanned over the substrate wafer. The three primary parameters of any implantation process are the type of dopant species, the accelerating energy used for implantation, and the dose of the source gas. The dose is the total number of ions that enter the wafer. Dose, ( ), can be calculated... [Pg.350]

The property characterizing the collimation of the beam formed is the spatial distribution 1(9, emitted particles. Due to the axial symmetry of the tube, the angle dependence is only on which is the angle of the emitted particles against the tube axis. The connection between 1(9) and the total rate of flow N is given by... [Pg.411]

In this wide-beam simulation, the initial condition is a Gaussian pulse with a phase perturbation. The waist of the initially collimated Gaussian was chosen to be 5 mm, the pulse duration is 500 fs, A = 248 nm, and the maximal intensity is 2 x 1014Wm-2. The total pulse energy is approximately 9mJ. A random phase perturbation is imposed on the pulse to initiate the transverse break-up of the pulse into multiple filaments (see Fig 13.3). We adjusted the amplitude of the perturbation such that it results in the filamentation onset after a few meters of propagation. [Pg.271]

Such a huge amplification factor does not exist for other DNA damages that do not involve strand breaks and CL. In this case, the quantity of fragments produced from a collimated electron beam is not sufficient for chemical analysis. To produce sufficient degraded material the new type of LEE irradiator described in the Section 19.2.2 can be used to bombard much more material. This technique allows the total mixture of products resulting from LEE bombardment of DNA to be... [Pg.537]

Total-ionisation cross sections are easiest to obtain by direct measurement (see section 2.2.2). Generally a well-collimated beam of nearly-monoenergetic electrons is passed through a gas or vapour target, and the positive ions formed are essentially all collected. It is necessary to use a thin target to ensure no secondary ionisation is produced. Then the collected positive current is given by (see equns. (2.8) and (2.11)). [Pg.24]


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