Rotational and oscillatory shear rheometry were used to quantify the flow behavior under minimal and significant solvent evaporation conditions for polymer solutions used to fabricate isoporous asymmetric membranes by the self‐assembly and non‐solvent induced phase separation (SNIPS) method. Three different A‐B‐C triblock terpolymer chemistries of similar molar mass were evaluated: polyisoprene‐
Controlled release of poly(vinyl sulfonate) scale inhibitor to extend reservoir treatment lifetime
Precipitate scale formation is a major issue for the oil industry, plugging equipment, and reservoirs and resulting in increased operational costs. Poly(vinyl sulfonate) (PVS) is often used as a scale inhibitor to prevent the formation of barium sulfate scale. However, PVS effectiveness is limited by its short lifetime in reservoir. In this article, PVS has been entrapped in polyelectrolyte complex nanoparticles (PECNPs), altering its charge and thus enabling improved adsorption on the rock surface. As the ionic strength of the surrounding brine increases, the PVS is then released from the PECNPs, making it available to inhibit scale formation gradually. Positively charged PECNPs were made using a combination of poly(ethyleneimine) (PEI) and PVS. After NPs optimization, static adsorption tests were performed, which confirm the nanoparticles' rapid and strong adsorption. An increase in the ionic strength of the displacing fluid was used to decompose the PECNPs structure and release the PVS into solution. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci.
- Award ID(s):
- 1632892
- NSF-PAR ID:
- 10078504
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Journal of Applied Polymer Science
- Volume:
- 136
- Issue:
- 12
- ISSN:
- 0021-8995
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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ABSTRACT b ‐polystyrene‐b ‐poly(4‐vinylpyridine) (ISV); polyisoprene‐b ‐polystyrene‐b ‐poly(N ,N ‐dimethylacrylamide) (ISD); and polyisoprene‐b ‐polystyrene‐b ‐poly(tert ‐butyl methacrylate) (ISB). Solvent evaporation resulted in the formation of a viscoelastic film typical of asymmetric membranes. Solution viscosity and film viscoelasticity were strongly dependent on the chemical structure of the triblock terpolymer molecules. A hierarchical magnitude (ISV > ISB > ISD) was observed for both properties, with ISV solutions displaying the greatest solution viscosity, fastest film strength development, and greatest strength magnitude. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci.2019 ,136 , 47038. -
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Abstract This study demonstrates that protein adsorption on end‐grafted, zwitterionic poly(sulfobetaine) (pSBMA) thin films depends on the grafting density, molecular weight, and ionic strength. Zwitterionic polymers exhibit ultralow nonspecific fouling (protein adsorption) and excellent biocompatibility. This picture contrasts with a recent report that soluble pSBMA chains bind proteins and alter the protein folding stability. To address this apparent contradiction, the dependence of protein adsorption on the chain grafting parameters is investigated: namely, the grafting density, molecular weight, and ionic strength. Studies compared the adsorption of phosphoglycerate kinase and positively charged lysozyme versus the scaled grafting parameter
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Membrane separations are simple to operate, scalable, versatile, and energy efficient, but their broader use is curtailed by fouling or performance decline due to feed component depositing on the membrane surface. Surface functionalization with groups such as zwitterions can mitigate the adsorption of organic compounds, thus limiting fouling. This can be achieved by using surface-segregating copolymer additives during membrane manufacture, but there is a need for better understanding of how the polymer structure and architecture affect the effectiveness of these additives in improving membrane performance. In this study, we aim to explore the impact of the architecture of zwitterionic copolymer additives for polyvinylidene fluoride (PVDF)-based membranes in fouling mitigation and ionic strength response. We prepared membranes from blends of PVDF with zwitterionic (ZI) copolymers with two different architectures, random and comb-shaped. As the random copolymer, we used poly(methyl methacrylate- random- sulfobetaine-2-vinyl pyridine) (PMMA- r -SB2VP) synthesized by free radical polymerization. The comb-shaped copolymer was synthesized by grafting SB2VP side-chains from a PVDF backbone by controlled radical polymerization. Membranes were fabricated from PVDF-copolymer blends containing up to 5 wt% ZI copolymer. Compared to the additive-free PVDF membrane, water permeance increased five-fold with 5 wt% addition of either copolymer. The comb copolymer additive led to better resistance to fouling by a saline oil-in-water emulsion and to simulated protein adsorption in Atomic Force Microscopy (AFM) force measurements. The additive architecture had a significant influence on how membranes respond to changes in feed salinity, which is known to affect intra- and inter-molecular interactions in zwitterionic polymers. The random copolymer containing membrane showed a small and mostly reversible decrease in its permeance with salinity. In contrast, the comb copolymer-containing membrane underwent a conformational reorganization in saline solutions that leads to an irreversible permeance decrease, increased zwitterionic group content on the membrane surface, and smoother surface topography. The higher mobility of the zwitterionic groups in the comb-shaped architecture facilitates reorganization of the zwitterionic side-chains in response to ionic strength. Overall, this study establishes a new approach for developing highly fouling resistant membranes and defines how the architecture of a zwitterionic copolymer additive impacts the ionic strength response and fouling resistance of the membrane.more » « less
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