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Direct indicating viscometer

Direct Indicating Viscometer. This is a rotational type instrument powered by an electric motor or by a hand crank. Mud is contained in the annular space between two cylinders. The outer cylinder or rotor sleeve is driven at a constant rotational velocity its rotation in the mud produces a torque on the inner cylinder or bob. A torsion spring restrains the movement. A dial attached to the bob indicates its displacement. Instrument constants have been so adjusted that plastic viscosity, apparent viscosity, and yield point are obtained by using readings from rotor sleeve speeds of 300 and 600 rpm. [Pg.652]

Figure 4-107. Typical flow curve of mud using a direct-indicating viscometer. Figure 4-107. Typical flow curve of mud using a direct-indicating viscometer.
Plastic Viscosity and Yield Point. Plastic viscosity and yield point measurements are obtained from a direct indicating viscometer. Due to the temperature effect on the flow properties of oil-base mud, the testing procedure is modified. The mud sample in the container is placed into a cup heater [23]. The heated viscometer cup provides flow property data under atmospheric pressure and bottomhole temperature. [Pg.657]

Gel Strength. The gel strength of oil-base muds is measured with a direct indicating viscometer exactly like that of water-base muds. [Pg.657]

The study was conducted to explore the use of this water-soluble LGC as a prospective drilling mud multi-functional additive and evaluate its thermal stability in both fresh-water and saline-water drilling muds. The mud rheological tests were performed according to the American Petroleum Institute (API] standard specifications by means of a direct-indicating viscometer with... [Pg.133]

Consistency Indices for the reciprocating capillary viscometers are calculated In a similar manner except that 1C 1s determined directly from log shear rate vs log shear stress data. [Pg.110]

Table I indicates good agreement between the molecular weight distribution statistics obtained by coupled GPC/Viscometer method and the nominal values for t BS 706. The discrepancy between the Mark-Houwink parameters obtained here and the reported values for polystyrene standard ( ) in THF at 25°C (i.e., a = 0,706 and k = 1.60 x 10 ) may in part be due to the uncertainty involved in the determination of the dead volume between DRI and viscometer detectors. Our simulation studies over a range of dead volume values (0 to 120u)l) showed that a and k are quite sensitive to the dead volume between the detectors. Larger dead volume results in smaller o and larger k values. This is a direct result of a clockwise rotation of log [q] vs. log M(v) curve (Figure 12) which occurs when the dead volume correction is applied in quantitative analysis. The effect on the molecular weight statistics, however, appeared to... Table I indicates good agreement between the molecular weight distribution statistics obtained by coupled GPC/Viscometer method and the nominal values for t BS 706. The discrepancy between the Mark-Houwink parameters obtained here and the reported values for polystyrene standard ( ) in THF at 25°C (i.e., a = 0,706 and k = 1.60 x 10 ) may in part be due to the uncertainty involved in the determination of the dead volume between DRI and viscometer detectors. Our simulation studies over a range of dead volume values (0 to 120u)l) showed that a and k are quite sensitive to the dead volume between the detectors. Larger dead volume results in smaller o and larger k values. This is a direct result of a clockwise rotation of log [q] vs. log M(v) curve (Figure 12) which occurs when the dead volume correction is applied in quantitative analysis. The effect on the molecular weight statistics, however, appeared to...
Since fluid shear rates vary enormously across the radius of a capillary tube, this type of instrument is perhaps not well suited to the quantitative study of thixotropy. For this purpose, rotational instruments with a very small clearance between the cup and bob are usually excellent. They enable the determination of hysteresis loops on a shear-stress-shear-rate diagram, the shapes of which may be taken as quantitative measures of the degree of thixotropy (G3). Since the applicability of such loops to equipment design has not yet been shown, and since even their theoretical value is disputed by other rheologists (L4), they are not discussed here. These factors tend to indicate that the experimental study of flow of thixotropic materials in pipes might constitute the most direct approach to this problem, since theoretical work on thixotropy appears to be reasonably far from application. Preliminary estimates of the experimental approach may be taken from the one paper available on flow of thixotropic fluids in pipes (A4). In addition, a recent contribution by Schultz-Grunow (S6) has presented an empirical procedure for correlation of unsteady state flow phenomena in rotational viscometers which can perhaps be extended to this problem in pipe lines. [Pg.143]

Here the relationship F /S is not a constant — when the shear rate varies, the shear stress does not vary in the same proportion or even necessarily in the same direction. The viscosity of such fluids will therefore change as the shear rate varies. Thus, the experimental parameters of the viscometer model, spindle and speed all have an effect on the measured viscosity. This measured viscosity is called the apparent viscosity and is accurate only when explicit experimental parameters are adhered to and indicated in the recorded measure. [Pg.29]


See other pages where Direct indicating viscometer is mentioned: [Pg.422]    [Pg.349]    [Pg.991]    [Pg.19]    [Pg.423]    [Pg.279]    [Pg.3375]    [Pg.188]    [Pg.316]    [Pg.118]   
See also in sourсe #XX -- [ Pg.652 ]




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