Journal
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
Volume 649, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.colsurfa.2022.129487
Keywords
Flocculation; Controlled radical polymerization; Polyacrylamide; Adsorption
Categories
Funding
- Campus Alberta Innovates Program (CAIP)
- Institute for Oil Sands Innovation (IOSI)
- Natural Sciences and Engineering Research Council of Canada (NSERC)
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This study investigates the effect of polyacrylamide dispersity on flocculation performance in a kaolinite clay system. It is found that lower dispersity polyacrylamides result in larger clay aggregates, and the low molecular weight fraction has less influence on aggregate size. These findings suggest that polymers with narrow molecular weight distributions can be used in lower dosages.
This article investigates the effect of polyacrylamide dispersity (broad and narrow molecular weight distributions) on their flocculation performance in a system of kaolinite clay suspended in water. A series of uniform chain length (dispersity, D = 1.04 - 1.35) polyacrylamide flocculants were synthesized using reversible addition fragmentation chain-transfer polymerization. These uniform polyacrylamides were used individually, as low dispersity flocculants, and in blends, as high dispersity flocculants. Flocculation of the kaolinite suspension was monitored using a focused beam reflectance measurement system where the chord-length distribution of the clay aggregates could be recorded in real-time. Polyacrylamide flocculants with lower dispersities made larger clay aggregates than those with lower dispersities at equal doses. In the polymer blends, the fraction of the high molecular weight component was the best indicator of aggregate size formation; the low molecular weight fraction influenced less the final aggregate size. These findings suggest that polymers with narrow molecular weight distributions can be used in lower dosages than standard high dispersity flocculants with a similar concentration of high molecular weight polymer chains.
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