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Relevant bibliographies by topics / Association of polymers

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Journal articles

Academic literature on the topic 'Association of polymers'

Author: Grafiati

Published: 28 June 2021

Last updated: 9 February 2022

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Journal articles on the topic "Association of polymers"

1

Shi, Lei Ting, Zhe Na Shen, Wei Zhou, Zhong Bin Ye, and Jun Feng Wang. "Study on the Performance of Hydrophobic Association Water-Soluble Polymer with Strong Association Ability." Advanced Materials Research 418-420 (December 2011): 232–36. http://dx.doi.org/10.4028/www.scientific.net/amr.418-420.232.

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In this article, the viscosifying abilities, rheological properties, and flow characteristics of hydrophobic association water-soluble polymer with high association ability were studied using technical methods of viscosity measurement, rheological and core flow experiments. The results illustrate that hydrophobic associated polymers with low molecular weight rely on a strong hydrophobic interaction, the intermolecular and intramolecular micellar structure formed in solution with a strong ability to increase viscosity. Hydrophobic association water-soluble polymer, comparing with partially hydr

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2

Shapiro, Karen, Colin Krusor, Fernanda F. M. Mazzillo, et al. "Aquatic polymers can drive pathogen transmission in coastal ecosystems." Proceedings of the Royal Society B: Biological Sciences 281, no. 1795 (2014): 20141287. http://dx.doi.org/10.1098/rspb.2014.1287.

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Gelatinous polymers including extracellular polymeric substances (EPSs) are fundamental to biophysical processes in aquatic habitats, including mediating aggregation processes and functioning as the matrix of biofilms. Yet insight into the impact of these sticky molecules on the environmental transmission of pathogens in the ocean is limited. We used the zoonotic parasite Toxoplasma gondii as a model to evaluate polymer-mediated mechanisms that promote transmission of terrestrially derived pathogens to marine fauna and humans. We show that transparent exopolymer particles, a particulate form o

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3

Wei, Ming-Hsin, Boyu Li, R. L. Ameri David, et al. "Megasupramolecules for safer, cleaner fuel by end association of long telechelic polymers." Science 350, no. 6256 (2015): 72–75. http://dx.doi.org/10.1126/science.aab0642.

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We used statistical mechanics to design polymers that defy conventional wisdom by self-assembling into “megasupramolecules” (≥5000 kg/mol) at low concentration (≤0.3 weight percent). Theoretical treatment of the distribution of individual subunits—end-functional polymers—among cyclic and linear supramolecules (ring-chain equilibrium) predicts that megasupramolecules can form at low total polymer concentration if, and only if, the backbones are long (>400 kg/mol) and end-association strength is optimal. Viscometry and scattering measurements of long telechelic polymers having polycyclooctadi

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4

Schertzer, Jeffrey W., and Eric D. Brown. "Use of CDP-Glycerol as an Alternate Acceptor for the Teichoic Acid Polymerase Reveals that Membrane Association Regulates Polymer Length." Journal of Bacteriology 190, no. 21 (2008): 6940–47. http://dx.doi.org/10.1128/jb.00851-08.

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ABSTRACT The study of bacterial extracellular polysaccharide biosynthesis is hampered by the fact that these molecules are synthesized on membrane-resident carrier lipids. To get around this problem, a practical solution has been to synthesize soluble lipid analogs and study the biosynthetic enzymes using a soluble system. This has been done for the Bacillus subtilis teichoic acid polymerase, TagF, although several aspects of catalysis were inconsistent with the results obtained with reconstituted membrane systems or physiological observations. In this work we explored the acceptor substrate p

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5

Okawa, Kaori, Jian Ping Gong, and Yoshihito Osada. "Self-Propagating Association of Zwitterionic Polymers Initiated by Ionene Polymers." Macromolecular Rapid Communications 23, no. 7 (2002): 423. http://dx.doi.org/10.1002/1521-3927(20020401)23:7<423::aid-marc423>3.0.co;2-f.

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6

Srebnik, Simcha. "Physical association of polymers with nanotubes." Journal of Polymer Science Part B: Polymer Physics 46, no. 24 (2008): 2711–18. http://dx.doi.org/10.1002/polb.21605.

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7

Zhang, Zhijie, Chongwen Huang, R. A. Weiss, and Quan Chen. "Association energy in strongly associative polymers." Journal of Rheology 61, no. 6 (2017): 1199–207. http://dx.doi.org/10.1122/1.4997586.

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8

Quan, Xie, Su, and Feng. "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 11, no. 10 (2019): 1702. http://dx.doi.org/10.3390/polym11101702.

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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-P

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9

Donato, Ricardo K., and Alice Mija. "Keratin Associations with Synthetic, Biosynthetic and Natural Polymers: An Extensive Review." Polymers 12, no. 1 (2019): 32. http://dx.doi.org/10.3390/polym12010032.

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Among the biopolymers from animal sources, keratin is one the most abundant, with a major contribution from side stream products from cattle, ovine and poultry industry, offering many opportunities to produce cost-effective and sustainable advanced materials. Although many reviews have discussed the application of keratin in polymer-based biomaterials, little attention has been paid to its potential in association with other polymer matrices. Thus, herein, we present an extensive literature review summarizing keratin’s compatibility with other synthetic, biosynthetic and natural polymers, and

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10

Peng, Yuankun, Tongkui Yue, Sai Li, et al. "Rheological and structural properties of associated polymer networks studied via non-equilibrium molecular dynamics simulation." Molecular Systems Design & Engineering 6, no. 6 (2021): 461–75. http://dx.doi.org/10.1039/d1me00017a.

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The physical polymer network formed by molecular association via non-covalent interactions between end groups alters a great many rheological properties of polymers and produces some fascinating rheological phenomena.

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