Ten peaks were detected in the feed solution by positive and negative ion modes (
Figure 5 and Table 3). A mass spectrum of the 10 peaks ranging from 113 to 494 of molecular weight was obtained. However, the compositions and names of the chemicals could not be identified because of the lack of mass resolution of the LC-MS/MS. These 10 peaks were not detected in the draw solution and product water, and they were perfectly rejected in the FO side and FO–MD system. The high rejection of positively and negatively charged TOrCs was consistent with the previous studies using the FO or FO–RO systems (Hancock
et al. 2011; Xie
et al. 2013a; Coday
et al. 2014). The rejection of charged TOrCs, such as pharmaceuticals in domestic wastewater, that are treated at the facility by a demonstration-scale sequencing batch membrane bioreactor system was greater than 80 and 99% in a bench-scale FO experiment and a hybrid FO–RO process, respectively (Hancock
et al. 2011). Rejection of negatively charged TOrCs tends to increase because of enhanced electrostatic repulsion between the FO membrane and solutes (Xie
et al. 2013a). Additionally, the formation of a larger hydrated layer around the ionic species may also affect the rejection of negatively charged TOrCs (Holloway
et al. 2014). The rejection of positively charged compounds follows the general principle of size exclusion (Coday
et al. 2014). The high rejection of positively charged TOrCs can be explained by a large hydrated radius of ionic species in an aqueous solution (Holloway
et al. 2014). Such high rejection of TOrCs was also observed in a pilot-scale FO–RO system for 40 d (Hancock
et al. 2011). In this pilot-scale experiment, TOrC rejection was greater than that observed in bench-scale experiments. This result was possibly due to membrane compaction, the establishment of a fouling layer, and optimized hydrodynamic conditions in the pilot-scale system (Hancock
et al. 2011).
Table 3Rejection of trace organic compounds (TOrCs) by the FO–MD system
. | Retention time (min)
. | FO side
. | FO–MD
. | Estimated molecular weight
. |
---|
Positive ion mode | | |
#1 | 1.55 | 100 | 100 | 250 |
#2 | 1.93 | 100 | 100 | 113 |
#3 | 7.29 | 100 | 100 | 264 |
#4 | 12.39 | 100 | 100 | 278 |
Negative ion mode | | |
#5 | 1.93 | 100 | 100 | 182 |
#6 | 7.27 | 100 | 100 | 181 |
#7 | 7.66 | 100 | 100 | 188 |
#8 | 7.99 | 100 | 100 | 188 and 194a |
#9 | 16.58 | 100 | 100 | 174 |
#10 | 18.58 | 100 | 100 | 494 |
. | Retention time (min)
. | FO side
. | FO–MD
. | Estimated molecular weight
. |
---|
Positive ion mode | | |
#1 | 1.55 | 100 | 100 | 250 |
#2 | 1.93 | 100 | 100 | 113 |
#3 | 7.29 | 100 | 100 | 264 |
#4 | 12.39 | 100 | 100 | 278 |
Negative ion mode | | |
#5 | 1.93 | 100 | 100 | 182 |
#6 | 7.27 | 100 | 100 | 181 |
#7 | 7.66 | 100 | 100 | 188 |
#8 | 7.99 | 100 | 100 | 188 and 194a |
#9 | 16.58 | 100 | 100 | 174 |
#10 | 18.58 | 100 | 100 | 494 |
Figure 5
Total ion current chromatogram (TICC) of trace organic compounds and mass spectra in each solution. (a) TICC of TOrCs in each solution. (b) Mass spectrum of peak #1. The numbers assigned to the peaks in Figure 5(a) correspond to those in Table 3. The value in parenthesis for each product water indicates the water temperature set in the draw solution.
Figure 5
Total ion current chromatogram (TICC) of trace organic compounds and mass spectra in each solution. (a) TICC of TOrCs in each solution. (b) Mass spectrum of peak #1. The numbers assigned to the peaks in Figure 5(a) correspond to those in Table 3. The value in parenthesis for each product water indicates the water temperature set in the draw solution.
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