Membrane fouling in engineering nanofiltration process for drinking water treatment: The spatial and chemical aspects

Abstract

Nanofiltration (NF) has become an established process for advanced treatment of drinking water, while membrane fouling remains as the main issue slowing the widespread application of the process. In this study, the key foulants were identified, and their spatial distribution and potential interactions were investigated based on a two-stage NF engineering project for municipal drinking water treatment. Over half a year of operation showed that the membrane fouling was mostly chemically reversible. Characterizations of the cleaning waste revealed that inorganic fouling dominated at both stages, which was mainly caused by the deposition of Al, Ca, and Si. While the overall fouling was much more severe at Stage 2, the organic fouling was the reverse. Autopsy of one full-size membrane element from each stage indicated that in addition to Al, P and humic acid-like compounds were abundant in the fouling layer for both stages despite the spatial differences. The spatial distribution of foulants was influenced by both concentration effects and presence of feed channel spacers. For the free membrane area, inorganic foulants and humic acid-like compounds had higher contents at Stage 2 than Stage 1. While for the membrane area contacting with spacers, Al and P at Stage 1 were 0.74 and 1.51 times higher than those at Stage 2, respectively. Moreover, statistical analysis, complexation experiments and engineering operation strongly supported that the residual Al and natural organic matter (NOM) were key foulants for the NF process, mainly by forming Al-NOM complexes. Besides the Al-NOM complexes, condensed phosphate, primarily sourced from the dosed phosphate-containing antiscalants, might also co-precipitate with Al or Al-NOM complexes.