Viscosity formation

The fraction of oil-in-place recoverable from conventional petroleum reservoirs varies greatly with the reservoir type, oil viscosity, formation pressure, production rate, and finesse employed. The positive displacement aspect of water drive reservoirs generally gives them the highest ultimate petroleum recoveries, up to 70% of the oil-in-place [14]. Estimates of ultimate recoveries possible from gas cap drive and dissolved gas drive types of reservoirs are usually much lower, 25-50% for the former and 10-30% for the latter. Recovery from gravity drainage reservoirs will be at the lower end of the ranges of the two gas drive reservoir types. 

Divalent Effect In the brine of low to medium sahnities (monovalent content), the viscosity of polyacrylamide solution increases as hydrolysis proceeds (increases). However, in the presence of divalents, the viscosity behavior will be determined largely by the divalent metal ion concentrations. As hydrolysis increases, more acrylic acid exists in the solution. Hydrolyzed polyacrylamides (negative carboxyl groups) interact strongly with divalent metal cations such as Csi and Mg ". This phenomenon is commonly associated with reduction in solution viscosity, formation of gels or precipitates. 

Viscose formation (dissolution of alkali cellulose by addition of carbon disulfide) ... 

Fluorescence enhancement can be based on the change in environment, such as change of polarity, dielectric strength, pH, viscosity, formation of hydrogen bonds. One principle makes use of polarity sensitive fluorescent probes such as dansyl derivatives or anilinonaph-thalene sulfonic acid, which show fluorescence enhancement properties upon binding to proteins, e.g., antibodies. The second variation is based on the fact that the fluorescence of a fluorescein-labeled analyte is quenched in the presence of heavy atoms, such as iodine. When the labeled probe binds to the antibody, this quenching is partially reversed. 

Time of the 1st data point (sec) . 6830B+04 Radius of invasion front (feet) . 4000B+00 Time of the 2nd data point (sec) . 2962B+05 Radius of invasion front (feet) . 8000B+00 Formation permeability (darcies) . lOOOE-02 Viscosity, formation fluid (cp) . 2000E+01 Trial No. 2 ... 

In oil bearing formations, the presence of polar chemical functions of asphaltenes probably makes the rock wettable to hydrocarbons and limits their production. It also happens that during production, asphaltenes precipitate, blocking the tubing. The asphaltenes are partly responsible for the high viscosity and specific gravity of heavy crudes, leading to transport problems. 

Oxidation first produces soluble oxygenated compounds of molecular weights between 500 and 3000 that increase the viscosity of oil then they polymerize, precipitate, and form deposits. Oxidation also causes formation of low molecular weight organic acids which are very corrosive to metals. 

This section will firstly consider the properties of oils in the reservoir (compressibility, viscosity and density), and secondly the relationship of subsurface to surface volume of oil during the production process (formation volume factor and gas oil ratio). 

The flowrate of oil into the wellbore is also influenced by the reservoir properties of permeability (k) and reservoir thickness (h), by the oil properties viscosity (p) and formation volume factor (BJ and by any change in the resistance to flow near the wellbore which is represented by the dimensionless term called skin (S). For semisteady state f/owbehaviour (when the effect of the producing well is seen at all boundaries of the reservoir) the radial inflow for oil into a vertical wellbore is represented by the equation ... 

The energetics and kinetics of film formation appear to be especially important when two or more solutes are present, since now the matter of monolayer penetration or complex formation enters the picture (see Section IV-7). Schul-man and co-workers [77, 78], in particular, noted that especially stable emulsions result when the adsorbed film of surfactant material forms strong penetration complexes with a species present in the oil phase. The stabilizing effect of such mixed films may lie in their slow desorption or elevated viscosity. The dynamic effects of surfactant transport have been investigated by Shah and coworkers [22] who show the correlation between micellar lifetime and droplet size. More stable micelles are unable to rapidly transport surfactant from the bulk to the surface, and hence they support emulsions containing larger droplets. 

When sulphur is melted viscosity changes occur as the temperature is raised. These changes are due to the formation of long-chain polymers (in very pure sulphur, chains containing about 100 (X)0 atoms may be formed). The polymeric nature of molten sulphur can be recognised if molten sulphur is poured in a thin stream into cold water, when a plastic rubbery mass known as plastic sulphur is obtained. This is only slightly soluble in carbon disulphide, but on standing it loses its plasticity and reverts to the soluble rhombic form. If certain substances, for example iodine or oxides of arsenic, are incorporated into the plastic sulphur, the rubbery character can be preserved. 

Evidence from the viscosities, densities, refractive indices and measurements of the vapour pressure of these mixtures also supports the above conclusions. Acetyl nitrate has been prepared from a mixture of acetic anhydride and dinitrogen pentoxide, and characterised, showing that the equilibria discussed do lead to the formation of that compound. The initial reaction between nitric acid and acetic anhydride is rapid at room temperature nitric acid (0-05 mol 1 ) is reported to be converted into acetyl nitrate with a half-life of about i minute. This observation is consistent with the results of some preparative experiments, in which it was found that nitric acid could be precipitated quantitatively with urea from solutions of it in acetic anhydride at —10 °C, whereas similar solutions prepared at room temperature and cooled rapidly to — 10 °C yielded only a part of their nitric acid ( 5.3.2). The following equilibrium has been investigated in detail ... 

The cellulose molecule contains three hydroxyl groups which can react and leave the chain backbone intact. These alcohol groups can be esterified with acetic anhydride to form cellulose acetate. This polymer is spun into the fiber acetate rayon. Similarly, the alcohol groups in cellulose react with CS2 in the presence of strong base to produce cellulose xanthates. When extruded into fibers, this material is called viscose rayon, and when extruded into sheets, cellophane. In both the acetate and xanthate formation, some chain degradation also occurs, so the resulting polymer chains are shorter than those in the starting cellulose. 

The industrial value of furfuryl alcohol is a consequence of its low viscosity, high reactivity, and the outstanding chemical, mechanical, and thermal properties of its polymers, corrosion resistance, nonburning, low smoke emission, and exceUent char formation. The reactivity profile of furfuryl alcohol and resins is such that final curing can take place at ambient temperature with strong acids or at elevated temperature with latent acids. Major markets for furfuryl alcohol resins include the production of cores and molds for casting metals, corrosion-resistant fiber-reinforced plastics (FRPs), binders for refractories and corrosion-resistant cements and mortars. 

To produce a spandex fiber by reaction spinning, a 1000—3500 molecular weight polyester or polyether glycol reacts with a diisocyanate at a molar ratio of about 1 2. The viscosity of this isocyanate-terrninated prepolymer may be adjusted by adding small amounts of an inert solvent, and then extmded into a coagulating bath that contains a diamine so that filament and polymer formation occur simultaneously. Reactions are completed as the filaments are cured and solvent evaporated on a belt dryer. After appHcation of a finish, the fibers are wound on tubes or bobbins and rewound if necessary to reduce interfiber cohesion. 

Permanent chemical crimp can be obtained by creating an asymmetric arrangement of the skin and the core parts of the fiber cross section. Skin cellulose is more highly ordered than core cellulose and shrinks more on drying. If, during filament formation in the spin bath, the skin can be forced to burst open to expose fresh viscose to the acid, a fiber with differing shrinkage potential from side-to-side is made, and crimp should be obtained (Fig. 5a). 

Incorporation of Flame Retardants in Fiber. Flame retardants suitable for cotton are also suitable for rayon. A much better product is obtained by incorporating flame retardants in the viscose dope before fiber formation. The principal classes of flame retardants used in viscose dope are tabulated aimuaHy (111). 

Atomization. A gas or Hquid may be dispersed into another Hquid by the action of shearing or turbulent impact forces that are present in the flow field. The steady-state drop si2e represents a balance between the fluid forces tending to dismpt the drop and the forces of interfacial tension tending to oppose distortion and breakup. When the flow field is laminar the abiHty to disperse is strongly affected by the ratio of viscosities of the two phases. Dispersion, in the sense of droplet formation, does not occur when the viscosity of the dispersed phase significantly exceeds that of the dispersing medium (13). 

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