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In situ study of aggregate sizes formed in chalcopyrite-quartz mixture using temperature-responsive polymers

Date

2018-05-08

Authors

Sung Ng, Wei
Connal, Luke
Forbes, Elizaveta
Mohanarangam, Krishna
Franks, G. V.

Journal Title

Journal ISSN

Volume Title

Publisher

Elsevier BV

Abstract

An interesting property of temperature-responsive polymers, such as poly(N-isopropylacrylamide) (PNIPAM), is the ability to behave as flocculants above a lower critical solution temperature (LCST). This study examines the aggregation of a chalcopyrite-quartz mixture using a sulfide-selective temperature-responsive polymer, P(NIPAM-co-ethyl xanthate methacrylate (EXMA)) in a continuously-sheared suspension, relative to polyacrylamide (PAM). The investigation was carried out in situ using imaging and Focused Beam Reflectance Measurement techniques to obtain real-time chord length distributions. While particle aggregates were observed in the presence of PNIPAM only upon heating above the LCST, P(NIPAM-co-EXMA) induced particle aggregation below the LCST, due to the attraction between the xanthate moiety and the sulfide surfaces. The largest aggregates were observed with P(NIPAM-co-EXMA) (1.5 MDa), followed by PNIPAM, PAM, and P(NIPAM-co-EXMA) (115 kDa). Particle aggregates formed with PAM did not exhibit further breakage under increasing shear to 1100 s^−1, while large-scale fragmentation was observed with the PNIPAM-based flocculants. Unlike PNIPAM, addition of P(NIPAM-co-EXMA) to suspension above the LCST was able to yield particle aggregation, attributed to the formation of charge-stabilised micelles. The influence of the shear rate on the size of the aggregates formed with P(NIPAM-co-EXMA) is unaffected by the polymer addition and measurement temperature below or above the LCST.

Description

Keywords

Temperature-responsive polymers, Particle aggregation, Aggregate size, Sulfide minerals, Shear breakage

Citation

Source

Advanced Powder Technology

Type

Journal article

Book Title

Entity type

Access Statement

License Rights

DOI

10.1016/j.apt.2018.04.027

Restricted until

2037-12-31