Time-Resolved and Steady-State Fluorescence Studies of Hydrophobically Modified Water-Soluble Polymers

2003 ◽  
Vol 107 (46) ◽  
pp. 12605-12621 ◽  
Author(s):  
J. Seixas de Melo ◽  
Telma Costa ◽  
Maria da G. Miguel ◽  
Björn Lindman ◽  
Karin Schillén
SPE Journal ◽  
2010 ◽  
Vol 16 (01) ◽  
pp. 43-54 ◽  
Author(s):  
Guillaume Dupuis ◽  
David Rousseau ◽  
René Tabary ◽  
Bruno Grassl

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.


1994 ◽  
Vol 79 (1) ◽  
pp. 167-177 ◽  
Author(s):  
John R. Ebdon ◽  
David M. Lucas ◽  
Ian Soutar ◽  
Linda Swanson

1982 ◽  
Vol 104 (15) ◽  
pp. 4146-4150 ◽  
Author(s):  
Michiya Itoh ◽  
Kunihiro Tokumura ◽  
Yoshifumi Tanimoto ◽  
Yoko Okada ◽  
Hiroshi Takeuchi ◽  
...  

2017 ◽  
Vol 17 (1) ◽  
pp. 86
Author(s):  
Marco Sandjaja ◽  
Maria Lucia Ardhani Dwi Lestari

This present study was conducted to investigate the effect of adding hydrophobically modified end-capped (HM) polymers with various polyethylene oxide (PEO) chain lengths on the structure and viscosity of anionic vesicles dispersion. A pronounced increase in viscosity was observed upon adding small amount of such polymers. Based on the dynamic light scattering (DLS) and small angle neutron scattering (SANS) analysis, 10 to 30 polymer molecules per vesicles can reach maximum viscosity and where polymer molecules can interconnect the vesicles without disrupting their structure. In addition, the kinetic stability of the vesicle dispersion also enhanced. From the measurement of the electrical conductivity of the dispersion, it was observed that the presence of the PEO and polypropylene oxide (PPO) group could induce the permeability of the vesicle membrane by altering their internal structure. Controlling viscosity of vesicles dispersion without changing its structure is useful for the further application of vesicles system such as in drug delivery, cosmetics and biomedical.


1993 ◽  
Vol 331 ◽  
Author(s):  
Shun-Yuan Wu ◽  
Carol A. Steiner

AbstractThe temperature response of hydrogels made from hydrophobically modified water soluble polymers is complicated by the fact that while the hydrophobilic backbone becomes dehydrated and thus less compatible with aqueous solvents as the temperature is increased, the hydrophobic side chains become more compatible. These opposing effects taken together will govern gel properties such as volume, storage modulus, etc. We will discuss the effects of temperature on the composition, volume and reheological properties of hydrogels made from hydrophobically modified hydroxyethyl cellulose (HMHEC) in aqueous solutions containing the surfactant sodium dodecyl sulfate (SDS).


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