scholarly journals Structure Formation of the Surface Layer of Soil as a Way to Prevent a Wind and Water Erosion

2012 ◽  
Vol 14 (4) ◽  
pp. 321 ◽  
Author(s):  
S. Aidarova ◽  
N. Bekturganova ◽  
M. Kerimkulova ◽  
K. Musabekov ◽  
A. Sharipova
Keyword(s):  
Structure Formation ◽  
Adsorbed Layer ◽  
Water Erosion ◽  
Water Soluble ◽  
Interpolymer Complex ◽  
Concentrated Suspensions ◽  
Water Soluble Polymers ◽  
Step Process ◽  
Soluble Polymers ◽  
Wind And Water Erosion

The present work describes the results of a study of structuring ability of water-soluble polymers such as polydimethyl diallyl ammonium chloride, saponification product of polyacrylonitrile (uniflok) and their interpolymer complex. On the kinetics of growth of Rehbinder’s plastic durability of coagulation structure of soil concentrated suspensions the effect of water soluble polymers and interpolymer complexes on the structure formation in the dispersions was studied. It was determined that the process is a two-step process which was caused by the adsorption step process: the binding of macromolecules with the soil surface by the random segments and conformational changes of macromolecules in the adsorbed layer. It was found that the soil stability structured by polymers against wind and water erosion increased with the concentration of water-soluble polymers. This is due to the increase of the structure formation in concentrated suspensions of soil in the presence of water soluble polymers. On the basis of the results it can be concluded that the treatment of mineral dispersions by water-soluble polymers alone or in the form of the interpolymer complex leads to a significant reduction of dust-and run-off of soil particles. The PDMDAAC/uniflok interpolymer complex in comparison with polymers reduces intensively the deflation which has a great economic and ecological importance.

Flow of Hydrophobically Modified Water-Soluble-Polymer Solutions in Porous Media: New Experimental Insights in the Diluted Regime

SPE Journal ◽  
2010 ◽  
Vol 16 (01) ◽  
pp. 43-54 ◽  
Author(s):  
Guillaume Dupuis ◽  
David Rousseau ◽  
René Tabary ◽  
Bruno Grassl
Keyword(s):  
Oil Recovery ◽  
Polymer Concentration ◽  
Adsorbed Layer ◽  
Water Soluble ◽  
Water Soluble Polymer ◽  
Improved Oil Recovery ◽  
Water Soluble Polymers ◽  
Resistance Factors ◽  
Soluble Polymers ◽  
Hydrophobically Modified

Summary The specific molecular structure of hydrophobically modified water-soluble polymers (HMWSPs), also called hydrophobically associative polymers, gives them interesting thickening and surface-adsorption abilities compared with classical water-soluble polymers (WSPs), which could be useful in polymer-flooding and well-treatment operations. However, their strong adsorption obviously can impair their injectivity, and, conversely, the shear sensitivity of their gels can be detrimental to well treatments. Determining for which improved-oil-recovery (IOR) application HMWSPs are best suited, therefore, remains difficult. The aim of this work is to bring new insight regarding the interaction mechanisms between HMWSPs and rock matrix and the consequences concerning their propagation in reservoirs. A consistent set of HMWSPs with sulfonated polyacrylamide backbones and alkyl hydrophobic side chains together with an equivalent WSP was synthesized and fully characterized. HMWSP and WSP solutions were then injected in model granular packs. As expected, with HMWSPs, high resistance factors (or mobility reductions, Rm) were observed. Yet, within the limit of the injected volumes, the effluent showed the same viscosity and polymer concentration as the injected solutions. A first significant outcome concerns the specificities of the Rm curves during HMWSP injections. Rm increases took place in two steps. The first corresponded to the propagation of the viscous front, as observed with WSP, whereas the second was markedly delayed, occurring several pore volumes (PV) after the breakthrough. This result is not compatible with the classical picture of multilayer adsorption of HMWSPs but suggests that injectivity is controlled solely by the adsorption of minor polymeric species. This hypothesis was confirmed by reinjecting the collected effluents into fresh cores; no second-step Rm increases were observed. Brine injections in HMWSP-treated cores revealed high residual resistance factors (or irreversible permeability reductions, Rk), which can be attributed to the presence of thick polymer-adsorbed layers on the pore surface. Nevertheless, Rk values strongly decreased when increasing the brine-flow rate. This second significant outcome shows that the adsorbed-layer thickness is shear-controlled. These new results should lead to proposing new adapted filtration and injection procedures for HMWSPs, aimed, in particular, at improving their injectivity.

New quenching media based on water-soluble polymers

1981 ◽  
Vol 23 (2) ◽  
pp. 104-106 ◽  
Author(s):  
A. V. Tolstousov ◽  
O. A. Bannykh
Keyword(s):  
Water Soluble ◽  
Water Soluble Polymers ◽  
Soluble Polymers ◽  
Quenching Media

scholarly journals SANS quantification of bound water in water-soluble polymers across multiple concentration regimes

Soft Matter ◽  
2021 ◽  
Author(s):  
Helen Yao ◽  
Bradley D. Olsen
Keyword(s):  
Neutron Scattering ◽  
Small Angle ◽  
Small Angle Neutron Scattering ◽  
Bound Water ◽  
Water Soluble ◽  
Wide Concentration Range ◽  
Water Molecules ◽  
Water Soluble Polymers ◽  
Soluble Polymers

Small-angle neutron scattering is used to measure the number of bound water molecules associating with three polymers over a wide concentration range. Different fitting workflows are evaluated and recommended depending on the concentration regime.

scholarly journals Flow Enhancement of Water-Soluble Polymers through Porous Media by Preshearing

2021 ◽  
Author(s):  
Mohsen Mirzaie Yegane ◽  
Julia Schmidt ◽  
Fatima Dugonjic-Bilic ◽  
Benjamin Gerlach ◽  
Pouyan E. Boukany ◽  
...  
Keyword(s):  
Porous Media ◽  
Water Soluble ◽  
Water Soluble Polymers ◽  
Soluble Polymers ◽  
Flow Enhancement
Sign in / Sign up

Export Citation Format

Share Document