scholarly journals Synthesis and Solution Properties of Hydrophobically Modified Polysaccharides

2017 ◽  
Vol 7 (2) ◽  
pp. 99 ◽  
Author(s):  
Vitaliy V. Khutoryanskiy
Keyword(s):  
Aqueous Solutions ◽  
Oil Recovery ◽  
Micelle Formation ◽  
Synthetic Methods ◽  
Solution Properties ◽  
Cellulose Ethers ◽  
Pectic Acid ◽  
Practical Applications ◽  
Amphiphilic Macromolecules ◽  
Hydrophobically Modified

Hydrophobically modified polymers are amphiphilic macromolecules mainly constituted of a hydrophilic backbone and hydrophobic side groups. In aqueous solutions these polymers undergo inter- or intra-molecular hydrophobic association, which results in unusual properties useful for a number of practical applications. The areas of application of these polymers include associative thickeners for enhanced oil recovery, pharmaceuticals, personal care formulations, coatings, adhesives, surfactants, emulsifiers, etc. This review presents the analysis of a literature data on preparation of hydrophobically modified polysaccharides (HMP) and their properties in aqueous solutions. Some of the synthetic methods used for hydrophobic modification of non-ionic (cellulose ethers, starch, dextran, pullulan, etc.), anionic (carboxymethylcellulose, hyaluronic<br />acid, pectic acid, alginic acid, heparin) and cationic  olysaccharides (chitosan) are presented. The methodology used for the investigation of solution properties of hydrophobically modified polysaccharides is discussed. Special attention is paid to aggregate and micelle formation in solutions of hydrophobically<br />modified polysaccharides, solubilization of hydrophobic compounds, their rheological properties and surface activity. The effects of polymer architecture (level of hydrophobic substitution, nature of hydrophobic groups, molecular weight of a hydrophilic backbone, etc.), concentration, temperature, presence of inorganic salts and organic solvents on solution properties of hydrophobically modified polysaccharides are discussed. Some applications of hydrophobically modified polysaccharides are briefly highlighted.

scholarly journals Rheological behaviours of guar gum derivatives with hydrophobic unsaturated long-chains

RSC Advances ◽  
2020 ◽  
Vol 10 (53) ◽  
pp. 32050-32057
Author(s):  
Minghua Zhang ◽  
Jianping He ◽  
Mingyu Deng ◽  
Peixin Gong ◽  
Xi Zhang ◽  
...  
Keyword(s):  
Aqueous Solutions ◽  
Guar Gum ◽  
Rheological Behaviors ◽  
Practical Applications ◽  
Hydrophobically Modified ◽  
Long Chains

The rheological behaviors of three hydrophobically modified guar gum derivatives in aqueous solutions were systematically studied for practical applications.

scholarly journals Interaction and Adsorption of Hydrophobically Modified Polyacrylamide on Silica and Asphaltene Surfaces

2019 ◽  
Vol 2019 ◽  
pp. 1-8 ◽  
Author(s):  
Wenjie Zou ◽  
Zichuan Fang ◽  
Zhijun Zhang ◽  
Zhenzhen Lu
Keyword(s):  
Oil Recovery ◽  
Adhesion Force ◽  
Interaction Mechanism ◽  
Surface Force ◽  
Industrial Applications ◽  
Oil Sand ◽  
Continuous Adsorption ◽  
Hydrophobically Modified Polyacrylamide ◽  
Hydrophobically Modified ◽  
Modified Polyacrylamide

The adsorption of polymers affects the cost and oil recovery in oil reservoir exploitation and the flocculation effect in the treatment of oil sand tailings. The adhesion and adsorption of a hydrophobically modified polyacrylamide (HMPAM), i.e., P(AM-NaAA-C16DMAAC), on silica and asphaltene were investigated using surface force measurements, thermodynamic analysis and quartz crystal microbalance with dissipation (QCM-D) measurement. Our study indicates that HMPAM polymer has strong interaction with both silica and asphaltene. The adhesion force of HMPAM on silica was stronger than that on asphaltene surface. Consistently, the adsorption of HMPAM was also greater on silica surface, with a more rigid layer formed on the surface. For HMPAM/silica system, the attractive interaction and the strong adhesion are mainly driven by the hydrogen bonding and electrostatic interaction. For HMPAM/asphaltene system, it is mainly due to hydrophobic interaction between the long hydrocarbon chains of HMPAM and asphaltene. Furthermore, continuous adsorption of HMPAM was detected and multiple layers formed on both silica and asphaltene surfaces, which can be attributed to the hydrophobic chains of HMPAM polymers. This work has illustrated the interaction mechanism of HMPAM polymer on hydrophilic silica and hydrophobic asphaltene surfaces, which provide insight into the industrial applications of hydrophobically modified polymer.

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.

scholarly journals Specific-Ion Effects Directed Noble Metal Aerogels: Versatile Manipulation for Electrocatalysis and Beyond

2019 ◽  
Author(s):  
RAN DU ◽  
YUE HU ◽  
René Hübner ◽  
Jan-Ole Joswig ◽  
Xuelin Fan ◽  
...  
Keyword(s):  
Porous Materials ◽  
Noble Metal ◽  
Noble Metals ◽  
Sol Gel ◽  
Synthetic Methods ◽  
Superior Performance ◽  
Gelation Mechanism ◽  
Practical Applications ◽  
Specific Ion Effects ◽  
Ion Effects

<div>Noble metal foams (NMFs) are a new class of functional porous materials featuring properties of both noble metals and monolithic porous materials, providing impressive prospects in catalysis, bio-sensing, plasmonic technologies, etc...Among reported synthetic methods to date, the sol-gel approach manifests overwhelming advantages for versatile synthesis of controlled nanostructured NMFs under mild condition. However, limited gelation methods and insufficient understanding of the underlying mechanism retards structure/composition manipulation of NMFs, hampering ondemand designing for practical applications. Herein highly tunable NMFs are fabricated at room temperature by activating specific-ion effects and regulating ion-nanoparticle interactions, affording various single/alloy NMFs with adjustable compositions (Au, Ag, Pd, Pt), ligament sizes (3.1~142.0 nm), and special morphologies. Their superior performance in programmable self-propulsion devices and electrocatalytic alcohol oxidation are demonstrated. This study provides not only a conceptually new route to fabricate and manipulate functional NMFs, but also an overall picture in understanding the gelation mechanism. It may pave the way for on-target designing versatile NMFs for various applications.</div>

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