Publication:
Formation and breakage of flocs using dual polymers

dc.contributor.authorsYukselen, M. A.; Gregory, J.; Soyer, E.
dc.date.accessioned2022-03-10T15:25:00Z
dc.date.accessioned2026-01-11T14:24:23Z
dc.date.available2022-03-10T15:25:00Z
dc.date.issued2006
dc.description.abstractThe effect of shear on the formation and break-up of flocs generated using cationic, anionic and non-ionic polymers, and dual combinations of these, has been investigated using conventional jar test procedure and by continuous optical monitoring. The breakage of flocs was followed at a high stirring speed, corresponding to average shear rate (G) of approximately 520 s(-1). Most of the breakage occurred within a few seconds of increasing the shear rate. After each breakage, the stirring rate was reduced to the original value of 50 rpm (G approximate to 23s(-1)) to allow the flocs to regrow. For cationic-anionic polymers case, the regrowth of flocs was fully reversible and the breakage factors were smallest indicating highest floc strength. In contrast, flocs formed using non-ionic polymer together with anionic or cationic did not produce as strong flocs. It is found that the sequence of polymer addition is not very significant for floc formation and reformation when the cationic-anionic dual system is used.
dc.identifier.doi10.2166/wst.2006.226
dc.identifier.eissn1996-9732
dc.identifier.issn0273-1223
dc.identifier.pubmed16752784
dc.identifier.urihttps://hdl.handle.net/11424/220057
dc.identifier.wosWOS:000238143200027
dc.language.isoeng
dc.publisherIWA PUBLISHING
dc.relation.ispartofWATER SCIENCE AND TECHNOLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectdual polyelectrolytes
dc.subjectdual polymers
dc.subjectfloc
dc.subjectfloc breakage
dc.subjectfloc strength
dc.subjectRE-FORMATION
dc.subjectFLOCCULATION
dc.subjectPOLYELECTROLYTES
dc.titleFormation and breakage of flocs using dual polymers
dc.typereview
dspace.entity.typePublication
oaire.citation.endPage223
oaire.citation.issue7
oaire.citation.startPage217
oaire.citation.titleWATER SCIENCE AND TECHNOLOGY
oaire.citation.volume53

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