Shear Stability of EOR Polymers

SPE Journal ◽  
2012 ◽  
Vol 17 (02) ◽  
pp. 335-339 ◽  
Author(s):  
A.. Zaitoun ◽  
P.. Makakou ◽  
N.. Blin ◽  
R.S.. S. Al-Maamari ◽  
A.R.. R. Al-Hashmi ◽  
...  

Summary An experimental study of shear stability of several high-molecular-weight polymers used as mobility-control agents in EOR projects has been performed in well-controlled conditions. The shearing device was made of a capillary tube with an internal diameter (ID) of 125 μm, through which polymer solution was injected at a controlled rate. The setup enables a precise measurement of the shear rate to which the polymer macromolecule is submitted. The degradation rate was measured by the viscosity loss induced by the passage into the capillary tube. The shear rate was gradually increased up to 106 sec–1 while checking degradation rate at each stage. Different commercial EOR polymer products were submitted to the test with polyacrylamide backbone and different substitution monomer groups. All macromolecules behave as flexible coils in solution. The parameters investigated were Molecular weight (between 6 and 20×106)Nature of substitution group (acrylate, ATBS/sulfonate, nVP/ vinyl-pyrrolidone)Salinity Polymer shear degradation increases with molecular weight and salinity, but decreases with the presence of acrylate, ATBS, and nVP. All results can be interpreted in terms of chain flexibility. The highly flexible polyacrylamide homopolymer is the most sensitive to shear degradation. Introduction of acrylate groups in the polymer chain induces some stability because of the rigidity provided by charge repulsion, which vanishes in the presence of high salinity because of the screening of acrylate negative charges. ATBS and VP groups, which are larger in size, provide significant chain rigidity, and thus better shear stability. It is also shown that some very-high-molecular-weight polymers, after passing the shearing device, attain a final viscosity lower than lower-molecular-weight products with the same chemical composition. This factor has to be taken into account in the final choice of a polymer for a given field application. As a comparison, although less popular today than 2 decades ago, xanthan gum (XG), which behaves like a semirigid rod, is shown to be much less sensitive to the shear-degradation test than the coiled polyacrylamides (Sorbie 1991).

e-Polymers ◽  
2011 ◽  
Vol 11 (1) ◽  
Author(s):  
Ming Duan ◽  
Shenwen Fang ◽  
Liehui Zhang ◽  
Fuxiao Wang ◽  
Peng Zhang ◽  
...  

AbstractAn experimental study of the flow-induced scission behaviour of four star hydrolyzed polyacrylamides (HPMA) with different arms during planar elongational flow in a cross-slot flow cell is described. The results showed that the shear stability of linear HPAM in distilled water was not essentially different from star HPAM. Polymer scission was not observed in either system in a shear rate range from 20,000 to 100,000s-1, which can be attributed to the strong polyelectrolyte behaviour of HPAM in distilled water. However, at the same shear rate, the star HPAMs exhibited superior shear stability in comparison to the linear HPAMs in aqueous solutions containing NaCl (CNaCl=0.2-1.0%wt) and, in particular, the initial reduction rate of relative viscosity (R) decreased with the degree of branching of the HPAMs. In addition, it was found that the R of five HPAMs in NaCl aqueous solutions exhibited an exponential dependence on shear rate, in which the coefficient C1 can be used to quantitatively evaluate shear stability. In star HPAM NaCl aqueous solutions, the increase of R with shear rate is very likely due to the decrease of the hydrodynamic radius (Rh) of these HPAMs, while the increase of R with NaCl concentrations can be attributed to the relatively low viscosity of these polymers at high NaCl concentrations.


1945 ◽  
Vol 18 (4) ◽  
pp. 874-876
Author(s):  
Richard F. Robey ◽  
Herbert K. Wiese

Abstract Peroxides are found in synthetic rubbers either as the result of attack by oxygen, usually from the air, or as a residue from polymerization operations employing peroxide catalysts. Because of possible detrimental effects of active oxygen on the properties of the rubber, a method of quantitative determination is needed. The concentration of peroxides in substances of lower molecular weight may be determined with ferrous thiocyanate reagent, either titrimetrically as recommended by Yule and Wilson or colorimetrically as by Young, Vogt, and Nieuwland. Unfortunately, many highly polymeric substances are not soluble in the acetone and methanol solutions employed in these procedures. This is also the case with hydrocarbon monomers, such as butadiene, containing appreciable concentrations of soluble high molecular weight polymers. Bolland, Sundralingam, Sutton and Tristram recommended benzene as a solvent for natural rubber samples and the reagent made up in methanol. However, most synthetic rubbers are not readily soluble even in this combination. The following procedure employs the ferrous thiocyanate reagent in combination with a solvent capable of maintaining considerable concentrations of synthetic rubber in solution. The solvent comprises essentially 20 per cent ethanol in chloroform.


Sign in / Sign up

Export Citation Format

Share Document