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Injection points pressure

How are the abrasives introduced into the machine With air compressors, the abrasive can be thrown into the open suction. If the suction or point of injection is pressurized, the abrasives can be introduced with a blow pot. An eductor should be used to put the abrasive leaving the blow pot into a fluidized state before introducing it to the main gas stream. A good starting point for the injection rate is 0.1 weight percent of gas flow. [Pg.750]

It was fortunate that, for the BURRO-9 test, RPTs were anticipated and a pressure transducer was located in the air about 30 m from the LNG injection point. The reflected overpressures at various times are shown in Table Vin. Also given on the same table are the TNT equivalents assuming a free-air, point-source explosion. Some equivalents were significantly higher than noted in the smaller Shell Pipeline tests. [Pg.133]

Because water is generally considered incompressible, applying pressure to the water table surface depresses the water proportionally to the water pressure. This pressure causes a radial depression of the water table about the pressure injection point. The depression dewaters a section of the smear zone and saturated zone proportionally to the pressure applied at the injection point. Dewatering of the smear zone increases the volume of the smear zone and... [Pg.885]

Because of the much better temperature homogeneity of the injected material, the required injection pressure is two to three times lower than in a plunger machine, under comparable conditions regions where the polymer is hardly molten cause a considerable increase in viscosity. Plunger machines are, therefore, only used for mass production of very small articles. A variant is the combination of screw and plunger, each in their own cylinder, both of which are discharged into a chamber just in front of the injection point the screw forms and transports the melt, which is the injected into the mould by the plunger. [Pg.207]

In another process optimization step, the cooling was further improved (from sufficient to efficient ) by using a lower temperature of the cooling liquid, with 0 ° C instead of 20 °C [35]. In this way, a yield of 39% was obtained with only three injection points, thus reducing the complexity of the microdevice and pressure drop (see Figure 5.8). [Pg.236]

Another injection point, which can be used with either extrusion of molding, is before the die or nozzle. A static mixer can be added that mixes the liquid color into the melt. The mixer has a series of channels that split and recombine the melt stream, giving good distributive mixing. Usually, the further downstream a liquid is added to a natural resin, the less chance there is of separation. This may require high pressure pumping to assure the liquid enters the melt stream which is under... [Pg.290]

The combined control of pressure, temperature profile and comonomer content as well as choice of reactor injection points pro-... [Pg.93]

Perhaps the key binary from an acid gas injection point of view is H2S + COz. From the study of Knapp et al. (1982) it can be seen that the PR and SRK equations result in excellent predictions for this binary with errors in the estimated bubble point pressure less than 1.5% and errors in the vapor phase composition less than 1 mol%. [Pg.98]

There is a second effect of the presence of methane in the injection gas. Methane, being more volatile than acid gas, tends to broaden the phase envelope. That is, the dew point pressures are significantly increased. The consequence of this is that it is now easier for the injection profile to intercept the phase envelope. In practical terms this means that presence of methane in the gas will tend to increase the likelihood that the acid gas will vaporize in the injection well. [Pg.224]

At reservoir conditions, the fluid is supercritical (density approximately 385 kg/m3 or 24.0 lb/ft3) and as we move up the injection well the fluid becomes a liquid (the pressure is greater than the bubble point pressure). [Pg.230]

A typical pressure profile obtained from the two transducers is presented in the Figure 2. Curve I along with points A, B and C illustrates the characteristic pressure prorile observed during the operation of the reactor. Meanwhile, curve II depicts the pressure profile inside the vacuum chamber. Point A of curve I indicates the pressure condition inside the Riser Simulator just prior to the hydrocarbon injection. Point B gives the Riser Simulator pressure at the end of the reaction period (just before evacuation commences) and Point C represents the equilibrium pressure once the pressures between the vacuum chamber and the Riser Simulator have stabilized. [Pg.313]

The spatially decoupled activation and deactivation can be also seen in a mode of PP known as low-pressure cascade arc torch (LPCAT) polymerization), which is described in Chapter 16. The activation of a carrier gas (e.g., argon) occurs in a cascade arc generator, and the chemical activation of a monomer or a treatment gas takes place near the injection point of the argon torch in the deposition chamber. The material deposition (deactivation) occurs in the deposition chamber. This is the same situation as the HWCVD, except that the mode of activation is different. [Pg.9]

The upstream pressure is smaller than P,i (tubing pressure at injection point), therefore no gas enters the tubing. The armulus pressure builds up until it reaches F. Then, injection into the tubing starts. [Pg.381]

Feed introduction Feed injection via pump Sample loop Feed container Check the volume behind the injection point Adjust the size, do not use too large loops Control temperature, stir, over-pressurize with nitrogen... [Pg.182]

The act of pumping liquid into a formation creates a zone of high pressure potential. Because of this, the entering fluid flows away from this zone in all directions, locally changing the normal groundwater flow pattern. At low pumping pressure, the excess pressure potential dissipates at short distances from the injection point, and it may be possible to establish new equilibrium conditions with steady-state inflow. [Pg.262]

Figure 4. Liquid pressure at injection point and water flow rale at outflow point. Figure 4. Liquid pressure at injection point and water flow rale at outflow point.

See other pages where Injection points pressure is mentioned: [Pg.236]    [Pg.1166]    [Pg.817]    [Pg.436]    [Pg.555]    [Pg.249]    [Pg.29]    [Pg.328]    [Pg.505]    [Pg.360]    [Pg.886]    [Pg.799]    [Pg.37]    [Pg.403]    [Pg.328]    [Pg.208]    [Pg.213]    [Pg.396]    [Pg.290]    [Pg.37]    [Pg.108]    [Pg.16]    [Pg.37]    [Pg.248]    [Pg.133]    [Pg.456]    [Pg.114]    [Pg.354]    [Pg.876]    [Pg.443]    [Pg.425]    [Pg.183]    [Pg.34]    [Pg.34]   


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