scholarly journals The Thermoviscosifying Behavior of Water-Soluble Polymer Based on Graft Polymerization of Pluronic F127 with Acrylamide and 2-Acrylamido-2-methylpropane Sulfonic Acid Sodium Salt

Polymers ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 1702 ◽  
Author(s):  
Quan ◽  
Xie ◽  
Su ◽  
Feng
Keyword(s):  
Molecular Weight ◽  
Polymer Solution ◽  
Sodium Salt ◽  
Polymer Concentration ◽  
Water Soluble ◽  
Pluronic F127 ◽  
Water Soluble Polymer ◽  
Practical Applications ◽  
Acid Sodium Salt ◽  
Methylpropionic Acid

A new concept of thermoviscosifying polymers is proposed to address the problems about decreasing viscosity of polymer solution under high temperatures. However, existing thermoviscosifying polymers have complicated synthesis processes and high costs, and both of them restrict the wide practical applications of thermoviscosifying polymers. Although polyethers have the characteristics of thermal gelatinization, they just display thermoviscosifying behaviors only under extremely high concentrations (>15 wt %). Therefore, the graft copolymerization of the commercialized Pluronic F127 (PEO100-PPO65-PEO100) with acrylamide and 2-acrylamide-methylpropionic acid sodium salt was studied here. A series of graft modified polyether polymers were prepared and it was expected to get thermoviscosifying polymers with high molecular weights and low association temperatures. Several factors on thermoviscosifying behaviors were investigated, such as polymerization condition, polymer concentration, hydrophilic monomer, molecular structure and molecular weight. It was also proven that the apparent viscosity of polymer solution is influenced by polymer concentration, molecular weight of polymer, and content of anion groups.

Modification of Near-Wall Turbulent Structure in Channel Flow by Dosing a Small Amount of Polymer Solution

2017 ◽  
Author(s):  
Yushi Okamura ◽  
Tomohiro Kurose ◽  
Yasuo Kawaguchi
Keyword(s):  
Velocity Distribution ◽  
Polymer Solution ◽  
Polymer Concentration ◽  
Water Soluble ◽  
Polymer Additives ◽  
Normal Velocity ◽  
Water Soluble Polymer ◽  
Low Speed ◽  
Wide Range ◽  
Near Wall

The phenomenon known as Toms effect can impart viscoelasticity to a water flow when a small amount of water-soluble polymer is added. The resulting viscoelastic fluid generates viscoelastic stress in the flow, dramatically reducing the turbulent stress. In this study, the spatial distribution of velocity is measured using a stereo-PIV method in the streamwise-spanwise plane parallel to the wall. Modification of the near wall turbulence by the polymer solution blown slowly from a permeable wall was investigated by analyzing the velocity distribution acquired by stereo-PIV measurements. Experimental results reveal that streamwise local mean velocity decreases as the dosed polymer concentration increases. The skewness factor at this height shifts from 0 to positive by adding the polymer, which indicates intensified turbulent coherent structure. Moreover, the spatial two-point correlation function calculated from streamwise velocity fluctuations maintains its high correlation with the streamwise direction. It is consistent with the finding from the instantaneous velocity distribution, which shows that the flection of low-speed streaks is suppressed. Next, it is revealed that the normal velocity at the wall for low-speed fluid is decreased dramatically by polymer additives. Moreover, applying the quadrant analysis, it is confirmed that ejection events are suppressed with decreasing normal velocity at the wall. Suppression of ejection motion affects to the turbulence in the log law layer. We conclude that this is one reason that turbulence is suppressed in a wide range of the shear layer by polymer additives present only in the vicinity of the wall.

Crosslinking of Guar and Guar Derivatives

SPE Journal ◽  
2007 ◽  
Vol 12 (03) ◽  
pp. 316-321 ◽  
Author(s):  
Cuiyue Lei ◽  
Peter E. Clark
Keyword(s):  
Polymer Solution ◽  
Critical Concentration ◽  
Polymer Concentration ◽  
Water Soluble ◽  
Solution Behavior ◽  
Water Soluble Polymer ◽  
Important Indicator ◽  
Low Concentrations ◽  
Wide Range ◽  
Overlap Concentration

Summary Crosslinking of guar and guar derivatives has played a major role in improving stimulation of oil and gas wells. While crosslinking has been used for a number of years, many facets of crosslinked systems are still not well understood. Part of the problem is that the traditional methods of determining the properties of crosslinked fluids work well for obtaining the data necessary for treatment design, but yield little insight into the nature of the crosslinked system. A good example of this is found in the development of low polymer concentration crosslinked gels. These gels are important because they lower costs and help to minimize formation damage. In this paper, methods for predicting crosslinkability at low concentrations are reported. The polymer literature is filled with methods for characterizing polymer solutions almost none of which find wide use in the development of crosslinked fracturing fluids. Dawson et al. (2000) first reported that the concentration at which a polymer solution transitions from dilute to semidilute could be used as a method for determining the potential for low concentration crosslinking in guar or guar-derivative solutions. To test this assertion, we have conducted a series of experiments that not only shows that the dilute-semidilute transition concentration is an important indicator for the polymers used in this study, but also presents a framework for exploring the potential of other polymer systems. These experiments show conclusively that low-polymer concentration crosslinking is strongly related to the value of the critical overlap concentration, c*. Both the critical overlap concentration and the critical crosslinking concentration increase in the order guar-3 < CMG < CMHPG < guar < HPG. In addition, we show that the critical crosslinking concentration for the range of polymer-crosslinking systems studied is correlated to the critical overlap concentration (). A strong case is presented for the ability to crosslink at low concentrations is a strong function of the polymer type and a weak function of the crosslinker type. Introduction Water-soluble polymers have been used for a number of years as thickening agents for stimulation fluids. Crosslinking was developed to improve the performance of these materials without increasing polymer concentration. Over the years, a number of different crosslinking agents have been used with success. There are several good discussions of polymer and crosslinking systems available (Economides and Nolte 1989; Gidley et al. 1989), and it is not the purpose of this paper to expand these discussions. Rather, we will approach the problem of crosslinking from the prospective of the molecular or solution properties that control or influence crosslinking. When a water-soluble polymer is hydrated, the viscosity of the resulting solution increases as a function of concentration. Starting at low concentrations and building to high concentrations, the viscosity appears to exhibit an exponential increase. This phenomenon has been studied for a wide range of polymer—solvent systems and seems to be universal. Early work divided the viscosity—concentration curve into two regions (Menjivar 1986; Robinson et al. 1982) that were separated at a critical concentration labeled c*. As the understanding of polymer solution behavior progressed and more sensitive instruments and experimental techniques were developed, the solution behavior was determined to be more complex (Rubinstein and Colby 2003).

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.

Synthesis of Ionic Hydrophobic Associating Polymer and it’s Aqueous Solution‘s Viscosity Characteristics

2014 ◽  
Vol 628 ◽  
pp. 120-124
Author(s):  
Fa Yong Feng ◽  
Pei Zhi Yu
Keyword(s):  
Polymer Concentration ◽  
Synthesis Method ◽  
Water Soluble ◽  
Soluble Polymer ◽  
Water Soluble Polymer ◽  
Viscosity Behavior ◽  
Hydrophobically Associating ◽  
Temperature Shear ◽  
Hydrolyzed Polyacrylamide ◽  
Associating Polymer

Brief introduction of research progresses of hydrophobically associating water soluble polymer, as well as a synthesis method of a hydrophobically associating water-soluble polymer P (AM/KAA/MAHB). Meanwhile the molecular structure is characterized, and the viscosity behavior of the ionic hydrophobic-associating polymer solution is analyzed. The influences of polymer concentration, temperature, shear rate and water salinity of the saline solution on apparent viscosity are discussed. The critical associating concentration of polymer in salt solutions and salt thickening effect are also studied. The results show that the polymer possesses obvious temperature resistance and salt tolerance compared with partially hydrolyzed polyacrylamide polymer.

scholarly journals The Preparation of Soluble Cellouronic Acid Sodium Salt by 4-Acetamide-TEMPO Mediated Oxidation of Ultrasound-Pretreated Parenchyma Cellulose from Bagasse Pith

2015 ◽  
Vol 39 (2) ◽  
pp. 267-275 ◽  
Author(s):  
Xin Gao ◽  
Keli Chen ◽  
Heng Zhang ◽  
Lincai Peng
Keyword(s):  
Sodium Salt ◽  
Water Soluble ◽  
Ultrasound Treatment ◽  
Ultrasonic Power ◽  
Cellouronic Acid ◽  
Carboxylate Content ◽  
Acid Sodium Salt ◽  
Oxidation Reactivity ◽  
Ft Ir ◽  
Bagasse Pith

Abstract The parenchyma cellulose isolated from bagasse pith was used as an alternative resource for preparation of water-soluble cellouronic acid sodium salt (CAS). The influence of ultrasound treatment on the cellulose was investigated for obtaining CAS by regioselective oxidization using 4-acetamide-TEMPO and NaClO with NaClO2 as a primary oxidant in an aqueous buffer at pH 6.0. The yield, carboxylate content and polymerization degree (DP) of CAS were measured as a function of ultrasonic power, agitating time and cellulose consistency by an orthogonal test. The ultrasound-treated conditions were further improved by discussion of ultrasonic power, the most important factor influencing the yield and DP. An optimized CAS yield of 72.9% with DP value (DPv) of 212 was found when the ultrasonic strength is 550 W, agitating time is 3 h and cellulose consistency is 2.0%. The oxidation reactivity of cellulose was improved by ultrasonic irradiation, whereas no significant changes in crystallinity of cellulose were measured after ultrasonic treatment. Moreover, the ultrasound treatment has a greater effect on yielding CAS from parenchyma cellulose than from bagasse fibrous' one. The CAS was further characterized by Fourier transform infrared spectroscopy (FT-IR) and Scanning electron microscopy (SEM).

Sign in / Sign up

Export Citation Format

Share Document