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Injection pressure values

Because C, 0 are the functions of the water content ratio, is also related to the strata incidence and water content ratio. Before developing an oil reservoir, in-situ stresses should be obtained firstly. Using the in-situ stress values and strata incidence, the maximum pore pressure can be calculated through numerical simulation. In this way, reasonable water injection pressure values can be decided. [Pg.636]

Strengthening Techniques Code-Deficient R/C Buildings, Table 2 Recommended resin viscosity and injection pressure values for diffeitait tnack widths (ETEP 2012)... [Pg.3538]

Process details may be summarized powder sizes are fine (usually < 20 Ilm) low (generally < 69 MPa (10,000 psi)) injection pressure low (ca I49°C) mol ding temperature shrinkage (molded part to finished size) typically 20% final part densities are usually 95—98% + of maximum pore-free density and ductility is exceptionally high, elongation values are > 30%. [Pg.185]

In ntosl respects the process is similar to the injection moulding of thermoplastics and the sequence of operations in a single cycle is as described earlier. For thermosets a special barrel and screw are used. The screw is of approximately constant depth over its whole length and there is no check value which might cause material blockages (see Fig. 4.50). The barrel is only kept warm (80-110°C) rather than very hot as with thermoplastics because the material must not cure in this section of the machine. Also, the increased viscosity of the thermosetting materials means that higher screw torques and injection pressures (up to 200 MN/m are needed). [Pg.305]

Influence of Intermolecular Spacing on Enzymic Hydrolysis of Lecithin Monolayers. When snake venom phospholipase A is injected under a lecithin monolayer, it splits lecithin into lysolecithin and free fatty acid. The change in polar groups of the monolayer results in a change of surface potential. However, if prior to injection of enzyme into the subsolution, a lecithin monolayer is compressed to such a surface pressure that the active site of the enzyme is unable to penetrate the monolayer, hydrolysis does not proceed. For monolayers of dipalmitoyl, egg, soybean, and dioleoyl lecithins the threshold surface pressure values at which hydrolysis does not proceed are 20, 30, 37, and 45 dynes per cm., respectively (40). This is also the same order for area per molecule in their surface pressure-area curves, indicating that enzymic hydrolysis of lecithin monolayers is influenced by the unsaturation of the fatty acyl chains and hence the intermolecular spacing in monolayers (40). [Pg.200]

From Eq. (5.19) it follows that the value of T, corresponding to minimal filling time for the given plastisol, is determined by the only parameter S which in turn is dependent on the injection pressure P0 and geometric factors (parameters a, b0, m, K are constants for individual plastisol at a given temperature T0). [Pg.120]

The analysis shows that the minimal filling time at maximal temperature of a hot mould Tm is attained at maximal acceptable injection pressure P0. Since the value of Tw is also limited by safety considerations (thermal decomposition), the optimal value of injection pressure must be chosen on the basis of this limitation on the value of T. ... [Pg.120]

Garcia et al. plotted Ap2/Ap as a function of for various values of pressure dependence b. They used a power law index n = 0.3 and two typical low and high injection pressures of 40 MPa (400 bar) and 100 MPa (1000 bar), respectively. Figure 4.17 presents a plot of the pressure increase as a function of the down-scaled thickness, (R. As expected, the pressure increases with a decrease in thickness and with an increase in the pressure dependence coefficient, b. The process that already begins with a high pressure requirement of 1000 bars,... [Pg.203]

Figures 8.44, 8.45, 8.46 and 8.47 present the dimensionless injection pressures and clamping forces. Values from these graphs can be used to estimate injection pressure and... Figures 8.44, 8.45, 8.46 and 8.47 present the dimensionless injection pressures and clamping forces. Values from these graphs can be used to estimate injection pressure and...
If we assume the compressibility is constant and equal to some average value and again assuming the injection is isothermal, after some manipulation the injection pressure can be calculated as follows ... [Pg.218]

One caution when using this equation It is possible that inserting the values for the parameters in this equation results in a negative injection pressure. Obviously, this cannot occur. Physically, this means that at some point in the injection well, the fluid begins to vaporize and there is a gas cap on the column of fluid. [Pg.220]

Figure 9.1 shows the injection profile and the phase envelope for this case. This is a relatively simple case since the fluid does not change phase in the wellbore. The calculated injection pressure is 8770 kPa (1272 psia), which is about 17% larger than the value of 7446 kPa (1080 psia) given by Lock (1997). [Pg.229]

The intrusion-extrusion data are presented as pressure vs AV plots, where AV is the volume variation of the system due to water penetration in the porosity. Derivative representations d(AV)/dP of the intrusion curves allow to determine precisely the range of injection pressures. AV values are expressed in mm per gram of bare silica. [Pg.199]

The significant improvement in flow properties of resin IV vs. V is evident from the data. First, the torque from Brabender mixing indicates that resin IV is an easier-flowing material (Table II). The lower torque values for IV indicate the necessity of a lower-energy input to mix the polymer melt. This lower rotational force therefore indicates the polymer melt has a lower melt viscosity. Secondly, injection-molding conditions demonstrate the improved processability of resin IV (Table III) in comparison with resin V. At the same injection cylinder temperatures, the injection pressure for the tensile bar and Izod/heat distortion bar molds is lowered by 300 psi and 250 psi, respectively. [Pg.147]

The hydrogenation mixture was prepared by stirring 0.15 dm formaldehyde separated aldol solution into 0.15 dm methanol (>99.8 % J. T. Baker). The reaction mixture was saturated with hydrogen for 10-15 min in order to remove dissolved oxygen. The solution was injected into the reactor and temperature and pressure values were adjusted to the desired values. Liquid samples were withdrawn at pre-determined intervals and the duration of the experiments varied depending on process conditions. [Pg.309]

Abstract This paper presents a model for the simulation of two phase flow phenomena in deformable fractured rocks. The main problem is that gas pressure may play an important role on the mechanical behavior specially if discontinuities exist or develop. Fracture aperture changes and fracture failure are accounted by the model. Aperture of the discontinuity is used as the main variable for permeability and capillary pressure variations. Injection pressures that show peak values before steady state regime is attained are obtained with the model as shown in some simulations performed. [Pg.31]

This analysis has been performed for different values of the gas flow rate. The behaviour was similar and the maximum gas pressures achieved are included in Table 2. It can be observed that a flow rate of 0.0576 g/h produces failure, which implies large aperture of the fracture, large permeability increase, sharp drop of the gas injection pressure and, consequently, unstable numerical solution. [Pg.35]

For example, the observed decrease in the shear viscosity with the addition of MAH and PENTA leads to lower pressure in the filling of the mold in the mold-injection operation. In fact, the injection pressure diminishes from 40,680 kPa for PET to 24,822 kPa in the system PET-clay-MAH (1 wt%) and to 13,790 kPa in the system PET-clay-PENTA under the same processing conditions. This corresponds to a threefold decrease in the viscosity. However, it is necessary to point out that the viscosity curves reported are built from simple shear rheometric flows. In the actual process operation, the fluid that fills the mold is subjected to a nonhomogeneous stress field, which is likely to develop slip at the walls and another complicated flow behavior [62]. In these circumstances, the in situ viscosity is probably lower than that measured in the rotational rheometer. Measurements of pressure drop versus flow rate made on the fluid that enters the mold would surely provide a more reliable value of the process viscosity, and hence a better evaluation of the effect of the nanoparticles on the flow behavior of PET. [Pg.587]

The mould cavity must be filled completely without any flash occurring. The simplest control for mould filling uses limit switches on the screw travel. These actuate after the correct volume of melt has been injected, reducing the injection pressure to a lower holding value. However, any melt leakage past the screw non-return valve, or at the nozzle, causes the part mass to vary, with a consequent variation in the product dimensions. A better, more direct, control method uses a melt pressure transducer in the mould, which detects the rapid pressure rise, once the mould is full the... [Pg.164]


See other pages where Injection pressure values is mentioned: [Pg.890]    [Pg.185]    [Pg.358]    [Pg.31]    [Pg.256]    [Pg.259]    [Pg.264]    [Pg.292]    [Pg.369]    [Pg.192]    [Pg.117]    [Pg.120]    [Pg.133]    [Pg.390]    [Pg.394]    [Pg.233]    [Pg.769]    [Pg.821]    [Pg.208]    [Pg.192]    [Pg.23]    [Pg.890]    [Pg.13]    [Pg.224]    [Pg.268]    [Pg.127]    [Pg.132]    [Pg.635]    [Pg.198]    [Pg.863]    [Pg.456]    [Pg.301]   
See also in sourсe #XX -- [ Pg.156 ]




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