TY - JOUR
T1 - Assessment of cross flow filtration for the size fractionation of freshwater colloids and particles
AU - Doucet, FJ
AU - Maguire, L
AU - Lead, Jamie
PY - 2005/7/15
Y1 - 2005/7/15
N2 - This research has evaluated the ability of cross-flow filtration (CFF) to perform correct size fractionation of natural aquatic colloids (materials from 1 nm to 1 mu m in size) and particles (>1 mu m) using scanning electron microscopy (SEM) combined with atomic force microscopy (AFM). SEM provided very clear images at high lateral resolution (ca. 2-5 nm), whereas AFM offered extremely low resolution limits (sub-nanometer) and was consequently most useful for studying very small material. Both SEM and AFM were consistent in demonstrating the presence of colloids smaller than 50 nm in all fractions including the retentates (i.e. the fractions retained by the CFF membrane), showing that CFF fractionation is not fully quantitative and not based on size alone. This finding suggests that previous studies that investigated trace element partitioning between dissolved, colloidal and particulate fractions using CFF may need to be re-visited as the importance of particles and large colloids may have been over-estimated. The observation that ultra-fine colloidal material strongly interacted with and completely coated a mica substrate to form a thin film has important potential implications for our understanding of the behaviour of trace elements in aquatic systems. The results suggest that clean, 'pure' surfaces are unlikely to exist in the natural environment. As surface binding of trace elements is of great importance, the nature of this sorbed layer may dominate trace element partitioning, rather than the nature of the bulk particle. (C) 2005 Elsevier B.V. All rights reserved.
AB - This research has evaluated the ability of cross-flow filtration (CFF) to perform correct size fractionation of natural aquatic colloids (materials from 1 nm to 1 mu m in size) and particles (>1 mu m) using scanning electron microscopy (SEM) combined with atomic force microscopy (AFM). SEM provided very clear images at high lateral resolution (ca. 2-5 nm), whereas AFM offered extremely low resolution limits (sub-nanometer) and was consequently most useful for studying very small material. Both SEM and AFM were consistent in demonstrating the presence of colloids smaller than 50 nm in all fractions including the retentates (i.e. the fractions retained by the CFF membrane), showing that CFF fractionation is not fully quantitative and not based on size alone. This finding suggests that previous studies that investigated trace element partitioning between dissolved, colloidal and particulate fractions using CFF may need to be re-visited as the importance of particles and large colloids may have been over-estimated. The observation that ultra-fine colloidal material strongly interacted with and completely coated a mica substrate to form a thin film has important potential implications for our understanding of the behaviour of trace elements in aquatic systems. The results suggest that clean, 'pure' surfaces are unlikely to exist in the natural environment. As surface binding of trace elements is of great importance, the nature of this sorbed layer may dominate trace element partitioning, rather than the nature of the bulk particle. (C) 2005 Elsevier B.V. All rights reserved.
KW - aquatic colloids and particles
KW - atomic force microscopy
KW - scanning electron microscopy
KW - cross-flow filtration
KW - fractionation
UR - http://www.scopus.com/inward/record.url?scp=21344434849&partnerID=8YFLogxK
U2 - 10.1016/j.talanta.2005.02.026
DO - 10.1016/j.talanta.2005.02.026
M3 - Article
C2 - 18970148
SN - 0039-9140
VL - 67
SP - 144
EP - 154
JO - Talanta
JF - Talanta
ER -