Examination of literature on colloidal dispersion gels for oil recovery

This paper examines literature that claims,suggests,or implies that floods with"colloidal dispersion gels"(CDGs)are superior to polymer floods for oil recovery.The motivation for this report is simple.If CDGs can propagate deep into the porous rock of a reservoir,and at the same time,provide resistance factors or residual resistance factors that are greater than those for the same polymer formulation without the crosslinker,then CDGs should be used in place of polymer solutions for most/all polymer,surfactant,and ASP floods.In contrast,if the claims are not valid,(1)money spent on crosslinker in the CDG formulations was wasted,(2)the mobility reduction/mobility control for CDG field projects was under-designed,and(3)reservoir performance could have been damaged by excessive loss of polymer,face-plugging by gels,and/or excessive fracture extension.From this review,the clear answer is that there is no credible evidence that colloidal dispersion gels can propagate deep into the porous rock of a reservoir,and at the same time,provide resistance factors or residual resistance factors that are greater than those for the same polymer formulation without the crosslinker.CDGs have been sold using a number of misleading and invalid arguments.Very commonly,Hall plots are claimed to demonstrate that CDGs provide higher resistance factors and/or residual resistance factors than normal polymer solutions.However,because Hall plots only monitor injection pressures at the wellbore,they reflect the composite of face plugging/formation damage,in-situ mobility changes,and fracture extension.Hall plots cannot distinguish between these effects-so they cannot quantify in situ resistance factors or residual resistance factors.Laboratory studiesdwhere CDG gelants were forced through short cores during 2-3 h-have incorrectly been cited as proof that CDGs will propagate deep(hundreds of feet)into the porous rock of a reservoir over the course of months.In contrast,most legitimate laboratory studies reveal that the gelation time for CDGs is a day or less and that CDGs will not propagate through porous rock after gelation.A few cases were noted where highly depleted Al and/or HPAM fluids passed through cores after one week of aging.Details about these particular formulations/experiments were sparse and questions remain about their reproducibility.No credible evidence indicates that the CDG can propagate deep into a reservoir(over the course of weeks or months)and still provide a greater effect than that from the polymer alone.With one exception,aluminum from the CDG was never reported to be produced in a field application.In the exception,Chang reported producing 1-20%of the injected aluminum concentration.The available evidence suggests that some free(unreacted)HPAM and aluminum that was associated with the original CDG can propagate through porous media.However,there is no evidence that this HPAM or aluminum provides mobility reduction greater than that for the polymer formulation without crosslinker.

NEW METHOD FOR EFFECTIVE VISCOSITY OF COLLOIDAL DISPERSIONS WITH PERIODIC MICROSTRUCTURES

One of the central theoretical problems in the colloid field is to determine the rheological relation between the macroscopic properties of colloidal suspensions and the microstructures of the systems. In this work, the authors develop a method of transformation field by which one call calculate the effective viscosity of an incompressible: viscous fluid containing colloidal particles (either solid particles: or liquid drops) fixed at the points of a periodic lattice. The effective viscosity of a colloidal dispersion of spherical particles is calculated. The predictions of the theory are in good agreement with the Einstein's formula for suspensions and the Taylor's formula for emulsions at low particle concentrations. At higher particle concentrations, the theory reproduces the results of Nunan and Keller. The method is also applicable to the viscosity of colloidal systems with non-spherical particles.

A THEORETICAL RESEARCH TO EFFECTIVE VISCOSITY OF COLLOIDAL DISPERSIONS

Colloidal dispersions are common in nature with wide industrial applications. One of the central theoretical problems in the field is to determine the rheological properties of the colloidal dispersion from the microstructures of the systems. Because of the difficulties associated with the boundary-value problems of the many-particle system, existing theories for colloidal suspensions are limited to low particle concentrations. In this work, a method of transformation field is developed by which one can calculate the effective viscosity of an incompressible viscous fluid containing colloidal particles ( either solid particles or liquid drops). The predictions of the theory are in goad agreement with the Einstein's formula for suspensions and the Taylor's formula for emulsions at low particle concentrations. At higher particle concentrations, the results of Nunan and Keller are produced. The method is also applicable to the viscosity of colloidal systems with non-spherical particles.

Polydisperse spherical colloidal silica particles：Preparation and application

A new industrial method has been developed to produce polydisperse spherical colloidal silica particles with a very broad particle size,ranging from 20-95 nm.The process uses a reactor in which the original seed solution is heated to 100 ℃,and then active silicic acid and the seed solution are titrated to the reactor continuously with a constant rate.The original seeds and the titrated seeds in the reactor will go through different particle growth cycles to form different particle sizes.Both the particles＇ size distribution and morphology have been characterized by dynamic light scattering（DLS）and the focus ion beam（FIB） system.In addition,the as-prepared polydisperse colloidal silica particle in the application of sapphire wafer＇s chemical mechanical polishing（CMP） process has been tested.The material removal rate（MRR） of this kind of abrasive has been tested and verified to be much faster than traditional monodisperse silica particles.Finally,the mechanism of sapphire CMP process by this kind of polydisperse silica particles has been investigated to explore the reasons for the high polishing rate.

Effect of pH on rheology of aqueous Al_(2)O_(3)/SiC colloidal system

The rheological behavior of aqueous Al_(2)O_(3)/SiC suspensions at different pH values was investigated by rheological measurement.Experimental results showed that at pH=3-6,Al_(2)O_(3) and SiC particles have opposite surface charges,and the binary suspensions have lower viscosity than the unary suspensions at shear rates of 0-300 s^(-1).Furthermore,at pH=3-12,the stability of the Al_(2)O_(3) component seemed to dominate the overall rheological behavior of the Al_(2)O_(3)/SiC binary suspensions.The tendency mentioned above showed little variations in various ionic strengths,particle diameters and component fractions.

Yield stress measurements and microstructure of colloidal kaolin powders clusterized and dispersed in different liquids

Rheologicat measurements of four colloidal kaolin powders dispersed in water, paraffinic oil and liquid rubber have been done at solid concentration （9 （VS/VL） in the range 8-33%. In quasi-static conditions the yield stress τ° values were derived. An S-shaped relationship between τ° and （9 exists, that allows to evaluate the percolation threshold θc values. In water θc ranges between 29% and 33%, while it is between 17% and 21% in oil and in liquid rubber. In water the microstructure units, i.e. the primary clusters among kaolin crystallites, are denser and bigger than the ones in the two other liquids. Furthermore, in quasistatic condition, the aqueous microstructure units have less tendency to cling together to form a network that can span all over the liquid phase. The different kaolin dispersions at θ equal to 22% are characterized by yield stress ranging between 7.S Pa and 59 Pa in water, 66-250 Pa in oil and 230-770 Pa in liquid rubber. It has been found that for any kaolin types the log τ°/ θ evaluated near to the percolation threshold is a conservative parameter of the three different liquids. These results are useful to design colloidal dispersions with selected microstructure.

Preparation of stable colloidal suspensions of superdisintegrants via wet stirred media milling

Superdisintegrants are cross-linked polymers that can be used as dispersants for fast release of drug nanoparticles from nanocomposite microparticles during in vitro and in vivo dissolution. Currently avail- able superdisintegrant particles have average sizes of approximately 5-130 μm, which are too big for drug nanocomposite applications. Hence, production of stable superdisintegrant suspensions with less than 5 μm particles is desirable. Here, we explore the preparation of colloidal suspensions of anionic and nonionic superdisintegrants using a wet stirred media mill and assess their physical stability. Sodium starch glycolate （SSG） and crospovidone （CP） were selected as representative anionic and nonionic superdisintegrants, and hydroxypropyl cellulose （HPC） and sodium dodecyl sulfate （SDS） were used as a steric stabilizer and a wetting agent/stabilizer, respectively. Particle sizing, scanning electron microscopy, and zeta potential measurements were used to characterize the suspensions. Colloidal superdisintegrant suspensions were prepared reproducibly. The extensive particle breakage was attributed to the swelling-induced softening in water. SSG suspensions were stable even in the absence of stabilizers, whereas CP suspensions required HPC-SDS for minimizing particle aggregation. These findings were explained by the higher absolute （negative） zeta potential of the suspensions of the anionic superdisintegrant （SSG） as compared with those of the nonionic superdisintegrant （CP）.

POLYMER COLLOIDS FORMED BY POLYELECTROLYTE COMPLEXATION OF VINYL POLYMERS AND POLYSACCHARIDES IN AQUEOUS SOLUTION

The polyelectrolyte complex formed from the polyanion and polycation was studied by turbidimetry, static and electrophoretic light scattering, and elementary analysis. Sodium salts of polyacrylate （PA） and heparin （Hep） were chosen as the polyanion, and hydrochloric salts of poly（vinyl amine） （PVA） and chitosan （Chts） as the polycation. Although these vinyl polymers and polysaccharides have remarkably different backbone chemical structures and linear charge densities, all the four combinations PA-PVA, PA-Chts, Hep-PVA, and Hep-Chts provide almost stoichiometric polyelectrolyte complexes which are slightly charged owing to the adsorption of the excess polyelectrolyte component onto the neutral complex. The charges stabilize the complex colloids in aqueous solution of a non-stoichiometric mixture, and the aggregation number of the complex colloids increases with approaching to the stoichiometric mixing ratio. The mixing ratio dependence of the aggregation number for the four complexes is explained by the model proposed in the previous study.

A Deblurring Procedure for Two-dimensional Small Angle X-ray Scattering Patterns

A general pre-processing procedure of the measured SAXS patterns for reducing the effect of beam stop and beam stop holder is described. A proper method for automatically choosing the regularization parameter is implemented. The method works out on the two-dimensional SAXS patterns. After deblurring, the corresponding two-dimensional patterns will be converted into one-dimensional integrated intensity distribution curves. We tested the program using both calculated artificial data and real experimental data such as polystyrene and poly（methyl methacrylate） latices. The deblurred results are satisfactory showing the effectiveness of the method. The deblurring process of a typical two-dimensional SAXS pattern using the Matlab based program can be completed in few seconds on normal personal computers.

Synthesis and Characterization of Polyaniline/Partially Phosphorylated Poly(vinyl alcohol) Nanoparticles

The polyaniline/partially phosphorylated poly（vinyl alcohol）（PANI/P-PVA） nanoparticles were prepared by the chemical oxidative dispersion polymerization of aniline monomer in 0.5 mol/L HC1 aqueous media with the partially phosphorylated poly（vinyl alcohol） （P-PVA） as the stabilizer and co-dopant. The PANI/P-PVA nanoparticles were characterized by transmission electron microscopy （TEM）, Fourier transform infrared spectroscopy （FTIR）, thermal gravimetric analysis （TGA）, X-ray diffraction （XRD）, electrical conductivity measurements and re-dispersion stability testing. All the results were compared with the properties of the conventional polyaniline in the emeraldine salt form （PANI ES）. It was found that the feeding ratio of P-PVA obviously affected the morphology, re-dispersion stability and electrical conductivity of the PANI/P-PVA nanoparticles. When the feeding ratio of P-PVA ranged from 40 wt% to 50 wt%, the PANI/P-PVA nanoparticles showed spherical shape with good uniformity, significant re-dispersion stability in aqueous media and good electrical conductivity.