Reverse
osmosis (RO) is widely employed to provide clean water
from nontraditional sources (e.g., seawater or municipal wastewater).
One of its key challenges is membrane fouling, which leads to reduced
flux and increased operational costs. Despite its practical relevance,
fundamental understanding of membrane fouling is limited. Toward this
end, we investigated calcium (Ca) and silicon (Si) fouling under real
RO feed conditions using μ-X-ray fluorescence (μ-XRF)
mapping and μ-X-ray absorption near-edge fine structure (μ-XANES)
spectroscopy. These techniques are distinctly suited to identify the
spatial distribution and (local) chemical speciation of foulants,
thereby providing unique insight into the mechanisms of fouling under
realistic conditions. Specifically, we investigated RO membranes harvested
from a pilot-scale RO system operated at the Orange County Water District
(OCWD) Groundwater Replenishment System (GWRS) Advanced Water Purification
(AWP) Facility, which received the same feed water as the full-scale
plant. Both Ca and Si were found to be abundant in the fouling layer.
Despite the use of a commercial antiscalant to inhibit mineral formation,
several Ca minerals were present in the fouling layer as minority
species, including sulfates, phosphates, and carbonates; most of these
minerals were found in particles that were aligned with the feed spacer
used to separate the membranes. In contrast, organic-bound Ca and
silica occurred across the entire membrane. Our work provides novel
insight into the synergistic mechanism of RO fouling by Ca, Si, and
organics on RO membranes.