Title:
pH tempted Micellization of β-Cyclodextrin based Diblock copolymer and its application in solid/liquid separation

dc.contributor.authorKiran Kiran
dc.contributor.authorRudramani Tiwari
dc.contributor.authorKranthikumar Tungala
dc.contributor.authorS. Krishnamoorthi
dc.contributor.authorKrishna Kumar
dc.date.accessioned2026-02-07T09:21:31Z
dc.date.issued2020
dc.description.abstractThis work focuses on facile synthesis of pH responsive diblock copolymers based on acrylamide (AM) and 2-Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) grafted on β-Cyclodextrin and have application in solid/liquid separation. β-CD based chain transfer agent (CTA) has been synthesized by one pot synthesis method. Three different grades of β-Cyclodextrin based Macro CTA were synthesized through RAFT polymerization technique. Macro CTA have been used further in synthesis of five different grades of β-CD grafted pH-responsive diblock copolymers i.e. (β-CD-PRP’s) by varying the amount of AMPS. The polymeric materials were characterized by Fluorescence Spectroscopy, FT-IR, GPC, 1H-NMR, SEM, TEM, TGA, and XRD. β-CD-PRP’s shows their micellization properties at acidic pH < 6.57 with polymer conc. > 0.336 mg/mL and has also been studied for removal of model contaminant (kaolin). Among all grades of diblock copolymers, grade 3 shows best performance in the removal of kaolin from aqueous solution at 7 and 5 pH values. [Figure not available: see fulltext.]. © 2020, The Polymer Society, Taipei.
dc.identifier.doi10.1007/s10965-020-02095-4
dc.identifier.issn10229760
dc.identifier.urihttps://doi.org/10.1007/s10965-020-02095-4
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/35613
dc.publisherSpringer
dc.subjectBlock copolymers
dc.subjectMicellization
dc.subjectRAFT polymerization
dc.subjectSolid/liquid separation
dc.subjectβ-Cyclodextrin based pH responsive polymers
dc.titlepH tempted Micellization of β-Cyclodextrin based Diblock copolymer and its application in solid/liquid separation
dc.typePublication
dspace.entity.typeArticle

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