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Base pressure

Natural-mbber-based pressure-sensitive adhesives can be cured by standard mbber curatives, eg, sulfur plus an accelerator (see Rubber, natural) ... [Pg.234]

A vacuum system can be constmcted that includes a solar panel, ie, a leak-tight, instmmented vessel having a hole through which a gas vacuum pump operates. An approximate steady-state base pressure is estabUshed without test parts. It is assumed that the vessel with the test parts can be pumped down to the base pressure. The chamber is said to have an altitude potential corresponding to the height from the surface of the earth where the gas concentration is estimated to have the same approximate value as the base pressure of the clean, dry, and empty vacuum vessel. [Pg.368]

In general, the test object caimot be heated above its operating temperature in space. As free molecular conditions are obtained around the object, it outgases and, if solar-spectmm photons impinge on the object, increases the release of gas. Because the object is in a vessel and the area of the hole lea ding to the gas pump is small compared with the projected interior area of the vessel, molecules originating from the test object can return to the test object provided that they do not interact in some manner with the vessel walls and the other components of the molecular environment. The object inside the vessel estabhshes an entirely different system than the clean, dry, and empty vacuum vessel. The new system no longer has the capabiUty to reach the clean, dry, and empty base pressure within a reasonable time. [Pg.368]

Figure 3.7. Variation of base pressure and velocity versus distance. Figure 3.7. Variation of base pressure and velocity versus distance.
Qb = flow rate, SCFD Pb = base pressure, psia Tb = base temperature, °R... [Pg.9]

Electron spectroscopic techniques require vacuums of the order of 10 Pa for their operation. This requirement arises from the extreme surface-specificity of these techniques, mentioned above. With sampling depths of only a few atomic layers, and elemental sensitivities down to 10 atom layers (i. e., one atom of a particular element in 10 other atoms in an atomic layer), the techniques are clearly very sensitive to surface contamination, most of which comes from the residual gases in the vacuum system. According to gas kinetic theory, to have enough time to make a surface-analytical measurement on a surface that has just been prepared or exposed, before contamination from the gas phase interferes, the base pressure should be 10 Pa or lower, that is, in the region of ultrahigh vacuum (UHV). [Pg.9]

Wherry, R.W., Resin dispersions for water based pressure sensitive adhesives. Pressure Sensitive Tape Council Seminar (May, 1979). [Pg.674]

Plant Failure Rate Data Base. Pressure Vessel Reliability. 4.4-1... [Pg.127]

C. Allowance for control valve (base pressure drop at full-open position [9]... [Pg.93]

B = base pressure drop for control valve t dth valve in wde-open position, psi. (see list above). [Pg.94]

G = gas specific gravity Z = compressibility correction term P = pressure, psi, absolute Pq = base pressure, (14.73 psi, absolute)... [Pg.121]

Base pressure drop for control valve from manufacturer, psi... [Pg.154]

Experiments were carried out in a pulse reactor system based on the TAP-2 reactor described by Cleaves et al. [3]. This consists of a small tubular reactor and a detector housed in a vacujun system pumped by a 1,500 Is" turbomolecular pump to a base pressure of... [Pg.677]

The apparatuses used for the studies of both ammonia synthesis emd hydrodesulfurization were almost identical, consisting of a UHV chamber pumped by both ion and oil diffusion pumps to base pressures of 1 x10 " Torr. Each chamber was equipped with Low Energy Electron Diffraction optics used to determine the orientation of the surfaces and to ascertain that the surfaces were indeed well-ordered. The LEED optics doubled as retarding field analyzers used for Auger Electron Spectroscopy. In addition, each chamber was equipped with a UTI 100C quadrupole mass spectrometer used for analysis of background gases and for Thermal Desorption Spectroscopy studies. [Pg.155]

During the last year we have built an FTMS instrument specifically designed for laser-induced thermal desorption from single-crystal surfaces. Figure 5 is a perspective drawing of the Instrument. The chamber is pumped by a 150 1/s ion pump and has a base pressure of 2.0 X 10- torr. Gases are Introduced through sapphire-sealed leak valves from a diffusion pumped gas manifold. [Pg.243]

ESCA measurements were performed with an AEI ES200 spectrometer equipped with an A1 anode (1486.6 gV) and operated at 12 kV and 22 mA with a base pressure of 4 x 10 torr. The Nl 2p,2> 3p ... [Pg.306]

HREELS experiments [66] were performed in a UHV chamber. The chamber was pre-evacuated by polyphenylether-oil diffusion pump the base pressure reached 2 x 10 Torr. The HREELS spectrometer consisted of a double-pass electrostatic cylindrical-deflector-type monochromator and the same type of analyzer. The energy resolution of the spectrometer is 4-6 meV (32-48 cm ). A sample was transferred from the ICP growth chamber to the HREELS chamber in the atmosphere. It was clipped by a small tantalum plate, which was suspended by tantalum wires. The sample was radia-tively heated in vacuum by a tungsten filament placed at the rear. The sample temperature was measured by an infrared (A = 2.0 yum) optical pyrometer. All HREELS measurements were taken at room temperature. The electron incident and detection angles were each 72° to the surface normal. The primary electron energy was 15 eV. [Pg.6]

Electrocatalytic activity of supported metal particles has been investigated on surfaces prepared in an ultrahigh vacuum (UHV) molecular beam epitaxy system (DCA Instruments) modified to allow high throughput (parallel) synthesis of thin-film materials [Guerin and Hayden, 2006]. The system is shown in Fig. 16.1, and consisted of two physical vapor deposition (PVD) chambers, a sputtering chamber, and a surface characterization chamber (CC), all interconnected by a transfer chamber (TC). The entire system was maintained at UHV, with a base pressure of 10 °mbar. Sample access was achieved through a load lock, and samples could be transferred... [Pg.572]

QMS) and an ellipsometer complete the setup. The typical pressure is in the range of 0.15-0.5 mbar. The deposition chamber has a volume of 180 1. During processing it is pumped by a stack of two Roots blowers and one forepump (total pumping capacity is about 1500 m /h) otherwise it is pumped by a turbo pump (4501/s), with which a base pressure of 10 mbar is reached. [Pg.165]

Estimate base pressure, assume column efficiency of 60 per alent to one stage. [Pg.579]

Note 100 mm was assumed to calculate the base pressure. The calculation could be repeated with a revised estimate but the small change in physical properties will have little effect on the plate design. 138 mm per plate is considered acceptable. [Pg.583]


See other pages where Base pressure is mentioned: [Pg.365]    [Pg.371]    [Pg.517]    [Pg.52]    [Pg.53]    [Pg.65]    [Pg.71]    [Pg.93]    [Pg.204]    [Pg.574]    [Pg.403]    [Pg.403]    [Pg.93]    [Pg.158]    [Pg.170]    [Pg.166]    [Pg.319]    [Pg.51]   
See also in sourсe #XX -- [ Pg.18 , Pg.131 ]




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