Probing Coagulation Behavior of Individual Aluminum Species for Removing Corresponding Disinfection Byproduct Precursors: The Role of Specific Ultraviolet Absorbance

Coagulation behavior of aluminum chloride and polyaluminum chloride (PACl) for removing corresponding disinfection byproduct (DBP) precursors was discussed in this paper. CHCl3, bromine trihalomethanes (THM-Br), dichloroacetic acid (DCAA) and trichloroacetic acid (TCAA) formation potential yields were correlated with specific ultraviolet absorbance (SUVA) values in different molecular weight (MW) fractions of humic substances (HS), respectively. Correlation analyses and principal component analysis were performed to examine the relationships between SUVA and different DBP precursors. To acquire more structural characters of DBP precursors and aluminum speciation, freeze-dried precipitates were analyzed by fourier transform infrared (FTIR) and C 1s, Al 2p X-ray photoelectron spectroscopy (XPS). The results indicated that TCAA precursors (no MW limits), DCAA and CHCl3 precursors in low MW fractions (MW<30 kDa) had a relatively good relations with SUVA values. These DBP precursors were coagulated more easily by in situ Al13 of AlCl3 at pH 5.0. Due to relatively low aromatic content and more aliphatic structures, THM-Br precursors (no MW limits) and CHCl3 precursors in high MW fractions (MW>30 kDa) were preferentially removed by PACl coagulation with preformed Al13 species at pH 5.0. Additionally, for DCAA precursors in high MW fractions (MW>30 kDa) with relatively low aromatic content and more carboxylic structures, the greatest removal occurred at pH 6.0 through PACl coagulation with aggregated Al13 species.


Introduction
Humic substances (HS), which widely exists in raw water, can react with chlorine in water treatment process to form halogenated disinfection byproducts (DBPs) [1]. For DBPs control, enhanced coagulation is considered to be one of the best available techniques (BATs) [2,3]. Aluminum salts, such as aluminum sulfate, aluminum chloride (AlCl 3 ) and polyaluminum chloride (PACl) coagulants, are commonly used for reducing DBP precursors in drinking water treatment [4][5][6][7][8]. Previous investigations demonstrated aluminum species showed in situ Al 13 species of AlCl 3 at pH 5.0 (or aggregated Al 13 of PACl at pH 6.0) were preferentially bound to DBP precursors with aromatic and carboxylic structures [7]. Other studies reported that Al 13 species selectively bound to carboxylic groups at pH 6.0, and to phenolic moieties at pH 8.0 [9].
Recently, the role of aluminum speciation in the coagulation has attracted more attention. Our previous study indicated both structure characterization of DBP precursors and aluminum speciation could affect coagulation. However, few associate the coagulation behavior of individual aluminum species with corresponding DBP using SUVA. Furthermore, the role of SUVA as an indicator of aromaticity in coagulation behavior still needs further investigation.
The primary objective of the present research was to probe coagulation behavior of aluminum species for removing corresponding DBP precursors. DBPs formation potential (DBPsFP) in different MW fractions (including CHCl 3 FP/DOC, THMFP-Br/DOC, DCAAFP/DOC and TCAAFP/DOC) were correlated with specific ultraviolet absorbance (SUVA) values. Correlation analyses (CA) and principal component analysis (PCA) were performed to examine the relationships between SUVA and different DBP precursors. To acquire more structural distribution, freeze-dried raw waters and flocs by AlCl 3 and PACl coagulation were analyzed by fourier transform infrared (FTIR). We further identified surface component of organics and aluminum in the flocs by C 1s and Al 2p X-ray photoelectron spectroscopy (XPS).

Jar Tests
The HS was extracted from the sediments of Hanshiqiao Wetland in Beijing, China. The elemental composition of C, H, N and O was 31.17, 4.07, 3.56, and 30.34 wt %, respectively. Fractionation of HS was performed on a stirred ultrafiltration cell device (Model 8200, Amicon, Millipore, USA) with nominal MW cutoffs of 3, 10, 30, 100, 300 kDa regenerated cellulose membranes (PL, 63.5mm, Millipore, USA). Details were in accordance with previous study [6]. Raw HS and each fraction were first diluted in 1 L of deionized water to form a DOC concentration of 4.83 mg/L (±0.06 mg/L). Sodium bicarbonate was added to produce a final alkalinity of 100 mg/L as CaCO 3 , potassium chloride was added to bring the ionic strength to 3.3 mmol/ L, and kaolinite was added to produce an approximate turbidity of 20 NTU. This solution was mixed for 2 h, and then left in a closed container overnight before it was used in jar tests. This interval allowed the clay material to equilibrate with the water.
Jar tests were performed on a programmable jar tester (MY3000-6, MeiYu, China) in 500 mL beakers at room temperature. After the coagulants were injected into the HA samples, 2 min of rapid mixing at 200 rpm, and 15 min of slow stirring at 40 rpm was provided, followed by 30 min of quiescent settling. The pH of solutions was adjusted during rapid mixing.
AlCl 3 Á6H 2 O (Guaranteed Reagent, Beijing Chemical Regents Company) and PACl with high Al 13 content (obtained from Prof. Baoyou Shi in Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences [28]) were used for all jar tests. The basicity value (OH/ Al molar ratio) of PACl is 2.1, and the content of Al 13 is 81.2%. After supernatants through 0.45 μm cellulose acetate membrane filters for testing DOC, UV 254 and DBPsFP, precipitates were freeze-dried for infrared and XPS analysis.

DBPs formation potential
Prior to the addition of chlorine, all water samples were adjusted to pH 7.0 ± 0.2. Buffer solution of NaOH/KH 2 PO 4 (pH 7.0) and HOCl stock solution (an applied chlorine dosage of 20 mg/L) were injected into each water sample, and then it was capped and put in a 20°C incubator. After the 72-hour incubation, residual chlorine in the water samples was measured by the DPD titrimetric method. All samples were found to have measurable free chlorine residual. Water samples were then added with sodium sulfite and analyzed to determine THMFP and HAAFP concentrations.

Characterization of flocs
The infrared spectra were obtained on a Nicolet 5700 FTIR spectrometer (Thermo Electron Corporation, U.S.A.), using 2-5mg of flocs in potassium bromide pellets. XPS analysis was performed on an X-ray photoelectron spectrometer (ESCALAB 250, Thermo VG Scientific, UK) with a monochromatized Al Kα X-ray source (1486.7 eV) working at 150 W and 15 kV. High resolution scans were conducted with pass energy of 20 eV and step size of 0.1 eV.

Statistical analyses
CA and PCA were performed with SPSS 13.0 software. PCA was conducted using the relative abundance of DBP precursors in different MW fractions by two principal components analyses. CA was used to examine the relationships between SUVA and different DBP precursors. Significance levels are reported as non-significant (NS) (p > 0.05), significant ( Ã , 0.05 > p > 0.01) or highly significant ( ÃÃ , p < 0.01).

Results and Discussion
DBPsFP in different MW fractions before and after coagulation Specific CHCl 3 FP, THMFP-Br, DCAAFP and TCAAFP yields in the individual MW fractions of raw waters are presented in Table 1. High MW fraction (>30 kDa) produced lower CHCl 3 FP, THMFP-Br, DCAAFP and TCAAFP yields, whereas 3-10k Da and <3 kDa fractions produced higher DBPsFP. The general trend was that lower MW fractions had more reactive DBPs precursors, especially for TCAA precursors. Organic matter in low MW with higher reactivity of DBPs formation was also observed by other researchers [14,15]. In contrast with THMsFP yields, DCAA and TCAA yields had higher formation potential. That is, DCAA and TCAA precursors were main DBPs precursors in each fraction. It was consistent with the finding that the relative concentration of HAAs usually was greater than THMs in high-SUVA waters [16,30]. Table 1 also summarizes the residual CHCl 3 FP, THMFP-Br, DCAAFP and TCAAFP specific yields in individual MW fractions after coagulation, respectively. Lower DBPsFP yields suggested greater removal efficiencies of DBP precursors by AlCl 3 and PACl coagulation. The greatest removal of specific TCAAFP yields occurred at pH 5.0 by AlCl 3 coagulation in all MW fractions. In contrast to TCAA precursors, AlCl 3 and PACl coagulation were not responsible for reducing the THM-Br precursors, especially for high MW fractions. Comparing with the original yields, residual THMFP-Br yields in >100k Da and 30-100k Da fractions all increased after coagulation. The specific THMFP-Br yields reached minimum at pH 5.0 by PACl coagulation. Increased THMFP-Br yields may be attributed to worse removals for these DBP precursors than average DOC removal by coagulation. For DCAA and CHCl 3 precursors, removals by coagulation were significantly different in high or low MW fractions. For DCAA precursors in low MW fractions (MW<30 kDa), the greatest removal was AlCl 3 coagulation at pH 5.0. In high MW fraction (>100 kDa and 30-100 kDa), the residual DCAAFP yields reached minimum (33.0 and 29.0 μg/mg DOC, respectively) at pH 5.0 by PACl coagulation. In contrast to DCAA precursors, the greatest removals of CHCl 3 precursors by coagulation were different in high MW fractions, but similar with DCAA precursors in low MW fractions. In high MW fractions (MW>30 kDa), the greatest removal of CHCl 3 precursors by coagulation was with PACl at pH 5.0. In low MW fractions (MW<30 kDa), the greatest removal was AlCl 3 coagulation at pH 5.0.

Correlations between SUVA values and individual DBPsFP in different MW fractions
SUVA is a good surrogate for aromatic content of organic matter. It has been reported that SUVA influences significantly on DBPs reactivity [11,15,31]. In this study, correlations of TCAAFP, THMFP-Br and DCAAFP, CHCl 3 FP yields with SUVA values in different MW fractions (including raw and coagulated waters) were investigated (Figs 1 and 2). Spearman's correlation coefficients (R) were calculated ( Table 2 and S1 Table in S1 File). Among the qualitative parameters, there was a significant correlation between SUVA and TCAAFP, CHCl 3 FP, DCAAFP yields (R = 0.727, 0.722, and 0.732, respectively. p < 0.01). In the regression lines, correlation coefficient (R 2 ) and slope were parameters for contribution of SUVA on DBPsFP, and intercept was a parameter for contribution of other function groups (e.g., carboxyl) for DBPsFP. As illustrated in Figs 1 and 2, the slopes and R 2 of correlations mostly increased with MW decreased. Thus, SUVA provided more contribution on DBPsFP in low MW fractions.
The SUVA values showed positive correlations with the TCAAFP yields in all MW fractions (Fig 1). SUVA-TCAAFP correlations had higher slopes and correlation coefficients, but lower intercepts in low MW fractions. SUVA is a good indicator of aromatic carbon contents, and higher SUVA values represent stronger aromaticity [31]. In this study, positive linear relationships and high slope of the SUVA-TCAAFP relations confirmed that aromatic carbon sites gave great contribution to TCAAFP in low MW fractions. S1 Table in S1 File also showed a significant correlation between SUVA and TCAAFP yields in >100 kDa, 30-100 kDa, 10-30 kDa and <10 kDa fractions (R = 0.710, 0.777, 0.824 and 0.828, respectively. p < 0.05).
However, in contrast to SUVA-TCAAFP, the correlations of SUVA and THMFP-Br were different. In high MW fractions (MW>30k Da), the SUVA values showed negative correlations with the yields of THMFP-Br in MW>100 and 30-100k Da fractions (R = -0.645 and -0.767, respectively. p < 0.05). Though the correlation coefficients of SUVA-THMFP-Br in low MW fractions were positive, the low slopes indicated that aromatic structures only did a little contribution to the THMFP-Br formation, especially in the 10-30k Da fraction. There was no obvious correlation between the SUVA and the THMFP-Br yields in the 10-30k Da fraction (R = 0.0135). The negative relationships in high MW fractions were explained by some researchers [16] that certain functional groups in DBP precursors may affect the formation of THM-Br. This result also compares favorably with the observations that bromine was more reactive with aliphatic precursors than with aromatic precursors, and the reverse was true for chlorine [32]. Through negative relationships between SUVA and THMFP-Br in high MW fractions, it can be concluded that aromatic structures with high MW were no contribution to THMFP-Br, but other structures (e.g., aliphatics) may be a contributor.
As present in Fig 2, the SUVA values also correlated with both DCAAFP yields and CHCl 3 FP yields in all MW fractions. The correlations of SUVA-DCAAFP and SUVA-CHCl 3 FP were   [16]. Their results indicated that TCAA precursors are relatively more hydrophobic than DCAA and THM precursors. Furthermore, comparing with the correlations of SUVA-CHCl 3 FP, higher intercepts of the SUVA-DCAAFP relations indicated that other functional groups (e.g., carboxyl) provided more contribution for DCAAFP. Some researchers presented that DCAA and TCAA species had different formation mechanisms or different precursors, while THMs may have relatively more aliphatic moieties as their precursors in addition to aromatic structures [1,16]. However, in this study, it should be noted that activated aromatic structures are still an important part for DCAA and CHCl 3 precursors, especially in low MW fractions. It can be inferred that different coagulation efficiencies for removing individual DBPsFP (Table 1) Fig 3 showed the property-property plots between first and second factor loadings. All the parameters except THMFPBr showed positive factor 1 loadings. Wherein, the THMFPBr component was less significant related to factor 1 axe than the other four parameters, while showed highly positive factor 2 loadings. The other four parameters (SUVA, TCAAFP, CHCl 3 FP and DCAAFP) were close to the factor 1 axis and neared zero for the factor 2 loadings. The PCA results indicated that TCAAFP, CHCl 3 FP and DCAAFP maybe had close relations with SUVA dominated by factor 1. Hence, the PCA in our present study could separate the characteristics of the SUVA with different DBPsFP.
The PCA factors 1 and 2 scores of all 40 samples are plotted in Fig 4. The figure showed a marked difference between individual MW samples. The scores of different MW samples were relatively scattered. This result indicated that the effect of SUVA to DBPsFP was variable by different MWs. In general, with the decreasing of MWs, the factor 2 scores of DBPsFP samples decreased accompanied with the increasing of factor 1 scores.
Most lower MWs samples clustered with higher factor 1 and lower factor 2 scores, with MW <3k Da samples ranging from -0.04 to 2.6 for PCA 1 and -1.08 to 0.48 for PCA 2, MW 3-10k Da samples ranging from -0.66 to 2.04 for PCA 1 and -1.71 to 0.37 for PCA 2, respectively. In contrast, most of the higher MWs samples were located in the regions with lower factor 1 and higher factor 2 scores (approximate -0.97 to 0.28 for PCA 1 and -1.2 to 2.43 for PCA 2 in MW 30-100kDa fractions, -0.89 to 0.15 for PCA 1 and -1.19 to 1.96 for PCA 2 in MW >100kDa fractions, respectively). While there was no apparent pattern for most of the MW 10-30kDa fractions with ranging from -1.22 to 1.40 for PCA 1 and -0.90 to 1.13 for PCA 2. Obviously, it can be identified that DBPsFP in lower MWs was mainly influenced by factor 1, while DBPsFP in higher MWs was mainly dominated by factor 2. Therefore, lower MW fractions were more relevant to SUVA index in our study.

Characterization of raw waters and flocs in MW fractions by FTIR
As illustrated in Fig 5a, FTIR spectra of raw waters indicated significant differences among the MW fractions. The MW>100k Da fraction showed very strong absorption at 1445 cm -1 . Pronounced absorbance at 1440-1460 cm -1 , which was assigned as C-H deformation vibration of aliphatic structure [33,34], became progressively weaker with a decrease in MW. It indicated an increase in aliphatic content with increasing MW. A point of interest was that peaks at 1655 and 1568 cm -1 were inversely related to the intensity of absorption in the 1445 cm -1 . The peak at 1620-1660 cm -1 and 1540-1570 cm -1 mainly due to aromatic C = C stretching (or C = O stretching of conjugated carbonyl groups) and C = O stretching vibration of ketones/quinones [33][34][35]. The intensities of bands in the 1655 and 1568 cm -1 were stronger in low MW fractions than those in high MW fractions, indicating higher contents of aromatic structures and carbonyl groups in low MW fractions. Additionally, shoulder peaks appeared at near 1386 cm -1 in <3k Da and 3-10k Da fractions also indicated higher carboxylic or other oxygen-containing groups in low MW fractions. This shoulder peak was commonly assigned to O-H deformation and C-O stretching of phenolic or carboxylic group [33,35]. Accordingly, it suggested that high MW fractions had more aliphatic carbon structures and low MW fractions had higher contents of aromatic structures and oxygen-containing groups. It was consistent with the results of relationships between SUVA and DBPsFP yields in different MW fractions (Figs 1-4) discussed above. Due to more aromatic structures and less aliphatic structures in low MW fractions, almost all SUVA-DBPsFP relations in MW<30k Da fractions had higher slopes and correlation coefficients (Figs 1 and 2).
FTIR analysis of the coagulation precipitates are presented in Fig 5 and Table 3. The region of 1440-1460 cm -1 was greatly reduced in intensity by coagulation. The peak at 1655 cm -1 corresponding to aromatic structures [33,35] shifted to lower frequency with higher energy (1620-1640 cm -1 ) and increased in intensity. 1630/2923 (1630/2854) values indicated the ratios of aromatic to aliphatic structures. The 1630/2923 (1630/2854) ratios of flocs reached maximum at pH 5.0 by AlCl 3 coagulation, while that achieved minimum mostly at pH 5.0 by PACl coagulation in all MW fractions. These results demonstrated the trends of aromatic and aliphatic moieties in the flocs under different coagulation conditions. This was consistent with the hypothesis proposed above (Table 1 and Figs 1 and 2) that different coagulation removal of individual DBPsFP was due to structural characteristics of DBPs precursors.
The C = O stretching band at 1568 cm −1 [34] also shifted to lower frequency (1540-1550 cm -1 ), but intensity decreased to less. The peak at 1386 cm -l , which belonged to carboxylic or other oxygen-containing groups [33,35], shifted to slightly higher frequency (1390-1410 cm -l ) and increased in intensity. The 1404/2923, 1542/2923 and 1103/2923 ratios corresponded to carboxyl/aliphatics, C = O/aliphatics and C-O/aliphatic, respectively. Due to high ratios, flocs by PACl coagulation at pH 6.0 had more carboxylic structures, C = O and C-O groups than other flocs in all MW fractions. Accordingly, flocs by PACl coagulation at pH 5.0 with lower 1404/2923, 1542/2923 and 1103/2923 ratios had more aliphatics in all MW fractions. These were consistent with the results from 1404/2854, 1542/2854 and 1103/2854 ratios. Additionally, the differences between flocs at individual coagulation conditions did not related with MW obviously. Therefore, more aromatic structures were removed by AlCl 3 coagulation at pH 5.0, while PACl coagulation at pH 6.0 and pH 5.0 removed more carboxylic structures and aliphatic structures, respectively. This agreed with previous research that Al 13 species selectively bound to carboxylic groups at pH 6.0 [9].

Characterization of composition on flocs surface by XPS analysis
Based on the results mentioned above, we further identified the surface composition of coagulation flocs by XPS. Fig 6 shows the Al 2p XPS spectra of freeze-dried flocs coagulated by AlCl 3 and PACl. Previous study indicated that tetrahedrally coordinated Al (Al IV , 73.7 eV) had a lower binding energy than octahedrally coordinated Al (Al VI , 74.2 eV) [36,37]. In this study, the scans showed two overlapping bands associated with two different Al 2p transitions with binding energies of 73.9 eV and 74.6 eV, which correspond to Al IV and Al VI , respectively. The Al IV /Al VI ratio of flocs by AlCl 3 coagulation at pH 5.0 was approximately 1:13.8 (Fig 6a), which clearly suggested that the flocs contained some amount of Al IV center. This was in accordance with the results of Al speciation in flocs and solution that in situ formed Al 13 were dominated aluminum species of AlCl 3 at pH 5.0-5.5. [4,6,7,[38][39][40]. However, in situ Al 13 -HA complexes formed at pH 5.0 eventually decomposed into oligomeric Al-HA flocs during coagulation process, only a small amount of Al 13 flocs were residual [7]. In this study, flocs still remained Al IV centers, which may originate from in situ Al 13 during coagulation. In the XPS spectrum of flocs by PACl coagulation at pH 5.0, the ratio of Al IV and Al VI was 1:12.1 (Fig 6b). Al IV /Al VI ratio observed was very close to the theoretical value in Al 13 molecules (1:12), where a central Al IV is surrounded by 12 Al VI [36,37]. It implied that preformed Al 13 species played dominated role in coagulation. However, on the surface of flocs by PACl coagulation at pH 6.0, observed Al IV /Al VI ratio was approximately 1:11.4. Some researchers indicated that preformed Al 13 polymers can form aggregated Al 13 clusters at pH 6.0 and higher pH conditions [7,41]. Lin et al. also found that some outer octahedral structures could decompose from Al 13 molecules during the formation of Al 13 aggregates [37]. In this study, due to decreased Al VI during Al 13 aggregation, the Al VI /Al IV ratio was less than 12. Thus, it suggested that Al 13 aggregates were in the flocs by PACl coagulation at pH 6.0. According to surface composition in Al flocs obtained from XPS analysis, predominant hydrolyzed Al species during coagulation can be concluded. For AlCl 3 , major species at pH 5.0 were in situ formed Al 13 . For PACl, preformed Al 13 remained stable at pH 5.0, while aggregated Al 13 clusters dominated at pH 6.0.
Background-subtracted C 1s XPS spectra of the flocs are shown in Fig 7, and the observed peaks are listed in Table 4. Six chemical states were fitted to the C 1s envelopes. Components associated with (1) [42] were included in the three C 1s spectra. According to these assignments, aromatic carbon (28.1%) in the spectrum of flocs with AlCl 3 at pH 5.0 (Fig 7a) was more than that of other flocs. Additionally, compared with other coagulation, flocs by PACl coagulation at pH 5.0 had more aliphatic carbon (25.7%), while flocs by PACl coagulation at pH 6.0 had more C-O (22.3%), C = O (10.7%) and C(O)O (carboxylic carbon, 10.8%). That is, AlCl 3 coagulation removed more aromatic at pH 5.0. On the other hand, more aliphatic structures and carboxylic structures were removed by PACl coagulation at pH 5.0 and pH 6.0, respectively. These results were in accordance with the FTIR analysis mentioned above.

Probing coagulation behavior of aluminum species for corresponding DBP precursors removal
On the basis of SUVA-DBPsFP correlations and FTIR, XPS results in this study, DBP precursors with corresponding characteristics were distinguished by MW and relations with SUVA values. Accordingly, coagulation behavior of aluminum species for DBP precursors differed from each other. Removal Behaviour of DBP during Aluminum Coagulation It can be indicated from the correlations of SUVA and TCAA (Figs 1-3) that main component of the TCAA precursors was aromatic structures, but THM-Br precursors had relatively low aromatic content. In particular, THM-Br precursors in high MW fractions had little aromatic structures. It agreed with the observation that THMs may have relatively more aliphatics as their precursors in addition to aromatic structures [1,16]. For DCAA precursors and CHCl 3 precursors, Observation from the SUVA-DBPsFP relations, clear differences among MW fractions can be found. On one hand, aromatic structures were important part for DCAA and CHCl 3 precursors in low MW fractions (MW<30 kDa). On the other hand, the SUVA-D-CAAFP relations and FTIR in MW>30 kDa fractions indicated that less aromatic structures in high MW fractions caused more contribution of other functional groups (e.g., carboxyl) on the DCAAFP. Furthermore, the FTIR results in this study suggested that high MW fractions contained more aliphatic structures.
According to the DBP precursors corresponding characteristics (MW and structure), the removals of DBP precursors by coagulation were distinguished. The greatest reduction of specific TCAAFP yields in all MW fractions occurred at pH 5.0 by AlCl 3 coagulation (Table 1). FTIR and XPS results in this study also confirmed that aromatic structures were removed by AlCl 3 coagulation at pH 5.0 to a more extent than other structures in all MW fractions. It Table 4. Binding energies, full widths at half maximum (FWHM) and percent of total C for different chemical peaks in the C 1s XPS spectra (Fig 7).  agreed with the previous study [7] that more DBP precursors with aromatic and carboxylic structures were removed by AlCl 3 than those by PACl at pH 5.0. TCAA precursors (relatively high aromatic content) regardless MW exhibited similar removal trends to that of aromatic structures. Aluminum salts coagulation was not responsible for removing THM-Br precursors. Especially in high MW fractions, almost all THM-Br yields per DOC increased after coagulation, especially in high MW fractions ( Table 1). The specific THMFP-Br yields reached minimum at pH 5.0 by PACl coagulation for all MW fractions. This agreed with FTIR results and XPS analysis that relatively more aliphatic structures were removed by PACl coagulation at pH 5.0. In contrast to average DOC values, THM-Br still had aliphatic structures as their precursors in all MW fractions. Thus, accordingly to the minimum THMFP-Br yields after coagulation, PACl at pH 5.0 were more responsible for coagulating THM-Br precursors with aliphatic structures and relatively low aromatic content without MW limits.
For DCAA precursors and CHCl 3 precursors, in low MW fractions (MW<30 kDa), the greatest removal for both DCAA and CHCl 3 precursors occurred at pH 5.0 by AlCl 3 coagulation (Table 1), which resembled the best removal of TCAA precursors. Furthermore, the greatest removal of DCAA precursors in high MW fractions (MW>30 kDa) occurred at pH 6.0 by PACl coagulation (Table 1). It was consistent with the FTIR and XPS results that more carboxylic structures could be removed by PACl coagulation at pH 6.0. Accordingly, DCAA precursors with MW>30 kDa had relatively more carboxylic structures as their precursors. Thus, more these DBP precursors were removed by PACl coagulation at pH 6.0. In contrast to DCAA precursors, the greatest removal of CHCl 3 precursors with MW>30 kDa were by PACl coagulation at pH 5.0 (Table 1). These results were consistent with the FTIR and XPS results that more aliphatic structures could be removed by PACl coagulation at pH 5.0. Therefore, similar to THM-Br precursors, CHCl 3 precursors in MW>30 kDa fractions with aliphatics and relatively low aromatic structures were removed preferentially by PACl coagulation at pH 5.0. 3. For DBP precursors with high aromatic content, AlCl 3 coagulation at pH 5.0 removed more TCAAFP, DCAA precursors (MW<30 kDa) and CHCl 3 precursors (MW<30 kDa). More DCAA precursors (MW>30 kDa) with relatively low aromatic content and more carboxylic structures were removed by PACl coagulation at pH 6.0. For DBP precursors with aliphatics and relatively low aromatic structures, THM-Br precursors and CHCl 3 precursors (MW>30 kDa) were preferentially.
Supporting Information S1 File. S1 Table: Correlation matrix of SUVA index and four DBPsFP in different MW fractions. S1 Fig: Property-property plots of PCA factor loadings between SUVA indexand four DBPsFP in different MW fractions. (RAR)