A Multienzyme Cascade Pathway Immobilized in a Hydrogen-Bonded Organic Framework for the Conversion of CO2.

The reduction of carbon dioxide to valuable chemicals through enzymatic processes is regarded as a promising approach for the reduction of carbon dioxide emissions. In this study, an in vitro multi-enzyme cascade pathway is constructed for the conversion of CO2 into dihydroxyacetone (DHA). This pathway, known as FFFP, comprises formate dehydrogenase (FDH), formaldehyde dehydrogenase (FaldDH), formolase (FLS), and phosphite dehydrogenase (PTDH), with PTDH serving as the critical catalyst for regenerating the coenzyme NADH. Subsequently, the immobilization of the FFFP pathway within the hydrogen-bonded organic framework (HOF-101) is accomplished in situ. A 1.8-fold increase in DHA yield is observed in FFFP@HOF-101 compared to the free FFFP pathway. This enhancement can be explained by the fact that within FFFP@HOF-101, enzymes are positioned sufficiently close to one another, leading to the elevation of the local concentration of intermediates and an improvement in mass transfer efficiency. Moreover, FFFP@HOF-101 displays a high degree of stability. In addition to the establishment of an effective DHA production method, innovative concepts for the tailored synthesis of fine compounds from CO2 through the utilization of various multi-enzyme cascade developments are generated by this work.

Arsenite S-Adenosylmethionine Methyltransferase Is Responsible for Antimony Biomethylation in Nostoc sp. PCC7120.

Antimony (Sb) biomethylation is an important but uninformed process in Sb biogeochemical cycling. Methylated Sb species have been widely detected in the environment, but the gene and enzyme for Sb methylation remain unknown. Here, we found that arsenite S-adenosylmethionine methyltransferase (ArsM) is able to catalyze Sb(III) methylation. The stepwise methylation by ArsM forms mono-, di-, and trimethylated Sb species. Sb(III) is readily coordinated with glutathione, forming the preferred ArsM substrate which is anchored on three conserved cysteines. Overexpressing arsM in Escherichia coli AW3110 conferred resistance to Sb(III) by converting intracellular Sb(III) into gaseous methylated species, serving as a detoxification process. Methylated Sb species were detected in paddy soil cultures, and phylogenetic analysis of ArsM showed its great diversity in ecosystems, suggesting a high metabolic potential for Sb(III) methylation in the environment. This study shows an undiscovered microbial process methylating aqueous Sb(III) into the gaseous phase, mobilizing Sb on a regional and even global scale as a re-emerging contaminant.

A Novel Whole-Cell Biosensor for Bioavailable Antimonite in Water and Sediments.

Antimony (Sb) is an emerging contaminant, and its on-site speciation analysis is central to the accurate evaluation of its bioavailability and toxicity. The whole-cell biosensors (WCBs) for Sb(III) are promising but challenging due to the lack of Sb(III)-specific recognition components. Here, we constructed a novel Sb(III)-specific WCB using an Sb(III) transcriptional regulator (antR) and its cognate promoter (Pant). To prevent the promoter leakage of Pant, an additional regulatory gene, antR, was inserted downstream of the Sb(III)-inducible promoter, improving the sensitivity of the WCB by an order of magnitude and reaching the detection limit at 0.009 µM, which is lower than the WHO drinking water standard of Sb. Moreover, the WCB with double antR showed a high specificity toward Sb(III) compared with interfering ions at 3 orders of magnitude higher concentrations. This WCB was capable of measuring Sb(III) bioavailability in natural waters and sediments on-site, and its results were not statistically different from the chemical analysis. The insights gained from this work demonstrate that the addition of regulatory genes prevents promoter leakage and improves the sensitivity of WCBs in field applications. IMPORTANCE Antimony (Sb) is a redox-sensitive pollutant ubiquitous in the environment. Sb(III) is dominant in the subsurface and is readily oxidized to less toxic Sb(V) upon exposure to air, and therefore, on-site Sb speciation analysis is essential to evaluate its bioavailability and toxicity. Dissolved Sb concentration and speciation can be determined accurately using on-site chemical sensors, but chemical sensors have difficulty determining the bioavailable Sb(III) that is taken up by the cells. Here, we constructed an Sb(III)-specific whole-cell biosensor (WCB) using double Sb(III) transcriptional regulators (antR) downstream of its cognate promoter Pant. With an additional antR, the sensitivity of the WCB was improved by approximately 10 times, and the promoter leakage commonly found in WCBs was inhibited. Integrated with a tea-bag design, the WCB is able to measure Sb(III) bioavailability in natural water and sediments on-site. This study demonstrates the importance of inserting one more regulatory gene to improve sensitivity.

Facet-Dependent Atomic Distances Shape Vanadate Adsorption Complexes on Hematite Nanocrystals.

The environmental fate of vanadate (V(V)) is significantly influenced by iron oxide nanocrystals through adsorption. Nevertheless, the underlying driving force controlling V(V) adsorption on hematite (Fe2O3) facets is poorly understood. Herein, V(V) adsorption on the {001}, {110}, and {214} Fe2O3 facets was explored using batch adsorption experiments, spectroscopic studies, and density functional theory (DFT) calculations. Adsorption experiments suggested that the order of V(V) adsorption capacity followed {001} > {110} > {214}. However, the affinity of V(V) to the {001} facet was the weakest, as evidenced by its least resistance to phosphate and sulfate competition. Our extended X-ray absorption fine structure (EXAFS) study indicated the formation of the inner-sphere monodentate mononuclear (1V) complex on the {001} facet and bidentate corner-sharing (2C) complexes on the {110} and {214} facets. Density functional theory (DFT) calculations showed the 1V complex is preferable when the adjacent Fe-Fe atomic distance is significantly larger than the O-O atomic distance of V(V). Otherwise, the 2C complex is formed if the distance is comparable. This determining factor in surface complex formation can be safely extended to other oxyanions that the compatibility in the atomic distance of Fe-Fe on Fe2O3 facets and O-O in oxyanions shapes the surface complex. The molecular-level understanding of the facet-dependent adsorption mechanism provides the basis for the design and application of oxyanion adsorbents.

Occurrence, Fate, Human Exposure, and Toxicity of Commercial Photoinitiators.

Photoinitiators (PIs) are a family of anthropogenic chemicals used in polymerization systems that generate active substances to initiate polymerization reactions under certain radiations. Although polymerization is considered a green method, its wide application in various commercial products, such as UV-curable inks, paints, and varnishes, has led to ubiquitous environmental issues caused by PIs. In this study, we present an overview of the current knowledge on the environmental occurrence, human exposure, and toxicity of PIs and provide suggestions for future research based on numerous available studies. The residual concentrations of PIs in commercial products, such as food packaging materials, are at microgram per gram levels. The migration of PIs from food packaging materials to foodstuffs has been confirmed by more than 100 reports of food contamination caused by PIs. Furthermore, more than 20 PIs have been detected in water, sediment, sewage sludge, and indoor dust collected from Asia, the United States, and Europe. Human internal exposure was also confirmed by the detection of PIs in serum. In addition, PIs were present in human breast milk, indicating that breastfeeding is an exposure pathway for infants. Among the most available studies, benzophenone is the dominant congener detected in the environment and humans. Toxicity studies of PIs reveal multiple toxic end points, such as carcinogenicity and endocrine-disrupting effects. Future investigations should focus on synergistic/antagonistic toxicity effects caused by PIs coexposure and metabolism/transformation pathways of newly identified PIs. Furthermore, future research should aim to develop "greener" PIs with high efficiency, low migration, and low toxicity.

Hydration of TiO2 Facets Regulates As(III) Adsorption: DFT and DRIFTS Study.

Hydration of TiO2 facets controls the reactions occurring at the mineral-water interfaces. However, the underlying mechanism of the facet-dependent hydration and the effect of hydration on contaminant adsorption are still ambiguous. Herein, arsenite [As(III)] adsorption on hydrated {001}, {100}, {101}, and {201} TiO2 was explored by integrating multiple characterizations and density functional theory (DFT) calculations. Our macroscopic adsorption results show an As(III) adsorption density order of {201} > {100} > {101} > {001}, though As(III) on each facet formed a bidentate binuclear structure, as evidenced by the extended X-ray absorption fine structure analysis. The in situ diffuse reflectance infrared Fourier transform spectroscopy analysis identified distinctive surface hydroxyls on four-faceted TiO2 upon water adsorption. The hydrated surface regulated the subsequent As(III) adsorption, giving an As(III) adsorption energy order of {201} (-0.95 eV) < {100} (-0.38 eV) < {101} (-0.005 eV) < {001} (0.04 eV) according to DFT calculations. The As(III) adsorption energy on hydrated facets was linearly correlated with the macroscopical As(III) adsorption density (R2 = 0.99, p < 0.05), revealing that the impregnable water binding highly suppressed the exchange of As(III) molecules with adsorbed water. Our study provided a novel insight into the facet-dependent interfacial adsorption.

Genome-Resolved Metagenomics and Metatranscriptomics Reveal that Aquificae Dominates Arsenate Reduction in Tengchong Geothermal Springs.

Elevated arsenic (As) is common in geothermal springs, shaping the evolution of As metabolism genes and As transforming microbes. Herein, genome-level microbial metabolisms and As cycling strategies in Tengchong geothermal springs were demonstrated for the first time based on metagenomic and metatranscriptomic analyses. Sulfur cycling was dominated by Aquificae oxidizing thiosulfate via the sox system, fueling the respiration and carbon dioxide fixation processes. Arsenate reduction via arsC [488.63 ± 271.60 transcripts per million (TPM)] and arsenite efflux via arsB (442.98 ± 284.81 TPM) were the primary detoxification pathway, with most genes and transcripts contributed by the members in phylum Aquificae. A complete arsenotrophic cycle was also transcriptionally active as evidenced by the detection of aioA transcripts and arrA transcript reads mapped onto metagenome-assembled genomes (MAGs) affiliated with Crenarchaeota. MAGs affiliated with Aquificae had great potential of reducing arsenate via arsC and fixing nitrogen and carbon dioxide via nifDHK and reductive tricarboxylic acid (rTCA) cycle, respectively. Aquificae's arsenate reduction potential via arsC was observed for the first time at the transcriptional level. This study expands the diversity of the arsC-based arsenate-reducing community and highlights the importance of Aquificae to As biogeochemistry.

New Mobilization Pathway of Antimonite: Thiolation and Oxidation by Dissimilatory Metal-Reducing Bacteria via Elemental Sulfur Respiration.

Antimony (Sb) mobilization is widely explored with dissimilatory metal-reducing bacteria (DMRB) via microbial iron(III)-reduction. Here, our study found a previously unknown pathway whereby DMRB release adsorbed antimonite (SbIII-O) from goethite via elemental sulfur (S0) respiratory reduction under mild alkaline conditions. We incubated SbIII-O-loaded goethite with Shewanella oneidensis MR-1 in the presence of S0 at pH 8.5. The incubation results showed that MR-1 reduced S0 instead of goethite, and biogenic sulfide induced the formation of thioantimonite (SbIII-S). SbIII-S was then oxidized by S0 to mobile thioantimonate (SbV-S), resulting in over fourfold greater Sb release to water compared with the abiotic control. SbIV-S was identified as the intermediate during the oxidation process by Fourier transform ion cyclotron resonance mass spectrometry and electron spin resonance analysis. The existence of SbIV-S reveals that the oxidation of SbIII-S to SbV-S follows a two-step consecutive one-electron transfer from Sb to S atoms. SbV-S then links with SbIII-S by sharing S atoms and inhibits SbIII-S polymerization and SbIII2S3 precipitation like a "capping agent". This study clarifies the thiolation and oxidation pathway of SbIII-O to SbV-S by S0 respiration and expands the role of DMRB in the fate of Sb.

Mechanistic Study for Antimony Adsorption and Precipitation on Hematite Facets.

Heterogeneous reactions at the mineral-water interface are of paramount importance in controlling the transport of contaminants. Herein, antimony (Sb) adsorption and subsequent precipitation on Fe2O3 facets were explored to understand its partitioning mechanisms by multiple complementary techniques. Our extended X-ray absorption fine structure spectroscopy and density functional theory results provided a consensus on the local coordination environment of Sb(III) and Sb(V) on Fe2O3 facets. We observed that Sb adsorption and the following precipitation are associated with both Sb concentrations and Fe2O3 facets, and a change in the Sb surface-binding mode from edge-sharing to corner-sharing is preferred in precipitation. Fe2O3 facets determine Sb binding structures, resulting in a facet-dependent transformation of adsorption to precipitation. The preferred corner-sharing complexes on the {001} facet facilitated the formation of Sb2O3 and NaSb(OH)6 precipitates at a lower Sb concentration compared with other two {110} and {214} facets. In addition, the facet-specific binding configuration renders a heterogeneous epitaxial growth of Sb2O3. Our study provides a molecular understanding of facet effects on Sb adsorption and precipitation on minerals.

Immobilization and transformation of co-existing arsenic and antimony in highly contaminated sediment by nano zero-valent iron.

Arsenic (As) and antimony (Sb) are usually coexistent in mine wastes and pose a great threat to human health. The As immobilization by nano zero-valent iron (nZVI) is promising, however, the stabilization for co-occurring As and Sb is not known. Herein, the immobilization and transformation of As and Sb in nZVI-treated sediments were evaluated using complementary leaching experiments and characterization techniques. Raw sediment samples from a gold-antimony deposit revealed the co-existence of ultrahigh As and Sb at 50.3 and 14.9 g/kg, respectively. Leaching results show that As was more efficiently stabilized by nZVI than Sb, which was primarily due to the soluble fraction that was readily absorbed by nZVI of As was higher. As the nZVI treatment proceeds, the oxidation and reduction of As and Sb occur simultaneously as evidenced by XPS analysis. The primary oxidant, hydroxyl radicals, was detected by EPR studies, proving the occurrence of nZVI induced Fenton reaction. This study sheds light on differences in the interaction and immobilization of nZVI with Sb and As in co-contaminated sediments.

Arsenic biotransformation in industrial wastewater treatment residue: Effect of co-existing Shewanella sp. ANA-3 and MR-1.

Shewanella sp. ANA-3 with the respiratory arsenate reductase (ArrAB) and MR-1 with ferric reduction ability always coexist in the presence of high arsenic (As)-containing waste residue. However, their synergistic impacts on As transformation and mobility remain unclear. To identify which bacterium, ANA-3 or MR-1, dominates As mobility in the coexisting environment, we explored the As biotransformation in the industrial waste residue in the presence of Shewanella sp. ANA-3 and MR-1. The incubation results show that As(III) was the main soluble species, and strain ANA-3 dominated As mobilization. The impact of ANA-3 was weakened by MR-1, probably due to the survival competition between these two bacteria. The results of micro X-ray fluorescence and X-ray photoelectron spectroscopy analyses further reveal the pathway for ANA-3 to enhance As mobility. Strain ANA-3 almost reduced 100% surface-bound Fe(III), and consequently led to As(V) release. The dissolved As(V) was then reduced to As(III) by ANA-3. The results of this study help to understand the fate of arsenic in the subsurface and highlight the importance of the safe disposal of high As-containing industrial waste.

Asenic removal from groundwater using granular chitosan-titanium adsorbent.

Arsenic (As) contamination poses an urgent environmental risk, and its removal from groundwater remains a challenge due to the lack of efficient adsorbents. Herein, a novel granular chitosan-titanium (CS-Ti) adsorbent was fabricated by the sol-gel method. Batch experiments show that As(V) adsorption on CS-Ti followed the pseudo-second-order kinetic model, and the adsorption isotherm conformed to the Freundlich model with the correlation coefficient of 0.99. In situ FTIR spectra revealed that the CS-Ti adsorbent was composed of amorphous TiOx and chitosan by forming C-O-Ti and N-Ti bonds, and the amorphous TiOx was responsible for As(V) adsorption. Rapid small-scale column tests show that 165.6 µg/L of As in groundwater were effectively removed in approximately 126-bed volumes, and the spent adsorbents were regenerated with 0.01 mol/L NaOH and maintained the adsorption efficiency after four cycles. This study provides a simple and practical route to fabricate adsorbents for water treatment.

Hairpin-Structured Magnetic SERS Sensor for Tetracycline Resistance Gene tetA Detection.

Antibiotic resistance genes (ARGs) have become emerging environmental contaminants, and the effective on-site detection of ARGs is urgently needed. Herein, we constructed a hairpin-structured magnetic sensor for the analysis of a widespread ARG, tetA, using surface-enhanced Raman scattering (SERS). The SERS sensor was assembled by immobilizing core-satellite structured Fe3O4@SiO2-Au with single-stranded DNA in a folded hairpin structure. The SERS sensor exhibited good sensitivity and specificity for the detection of laboratory-synthesized tetA ssDNA fragments. In addition, this SERS strategy is the first of its kind to be employed for monitoring environmental samples in the field, with a limit of detection reaching as low as 25 copies µL-1. Univariate and multivariate linear regression equations verify the practicability of the SERS sensor for quantitative tetA determination, showing the prospect for an amplification-free alternative platform for sensitive and reliable on-site detection of ARGs in the environment.

Genetic Identification of Antimonate Respiratory Reductase in Shewanella sp. ANA-3.

Microbial antimonate [Sb(V)] respiratory reduction is an important process regulating Sb redox transformation in the environment. However, little is known about the microbial respiratory reductase for Sb(V). Herein, we report Sb(V)-respiring reduction by Shewanella sp. ANA-3 through an arsenate respiratory reductase encoded by arrAB. Incubation experiments showed that Shewanella sp. ANA-3 mediated Sb(V)-respiring reduction, which was dependent on the cell concentration. Both protein analysis and reverse transcriptase-polymerase chain reaction results revealed that arrAB was highly expressed in Sb(V)-respiring reduction. In vivo evidence with mutants indicated that neither ANA-3-ΔarrA nor ANA-3-ΔarrB was capable of reducing Sb(V) as efficiently as the wild type, whereas complementation by the wild-type sequences of arrA and arrB rescued the mutants' ability. Our in vitro results showed that ArrAB purified by His-Tag was able to mediate Sb(V) reduction, though with much suppressed catalytic kinetics compared with As(V) reduction. The cell-concentration-dependent reduction of Sb(V) was regulated by quorum sensing via the luxS gene. This study opens a new chapter in the mechanistic understanding of microbial Sb(V) respiratory reduction.

Enhanced Hydrolysis of p-Nitrophenyl Phosphate by Iron (Hydr)oxide Nanoparticles: Roles of Exposed Facets.

Iron (hydr)oxide nanoparticles are one of the most abundant classes of naturally occurring nanoparticles and are widely used engineered nanomaterials. In the environment these nanoparticles may significantly affect contaminant fate. Using two goethite materials with different contents of exposed {021} facet and two hematite materials with predominantly exposed {001} and {100} facets, respectively, we show that exposed facets, one of the most intrinsic properties of nanocrystals, significantly affect the efficiency of iron (hydr)oxide nanoparticles in catalyzing acid-promoted hydrolysis of 4-nitrophenyl phosphate (pNPP, selected as a model organophosphorus pollutant). Attenuated total reflectance Fourier-transform infrared spectroscopy analysis and density functional theory calculations indicate that the pNPP hydrolysis reaction on the iron (hydr)oxide surface involves the inner-sphere complexation between the phosphonate moiety of pNPP and the surface ferric iron (Fe(III)), through ligand exchange with primarily the singly coordinated surface hydroxyl groups of iron (hydr)oxides. Both the abundance and affinity of these adsorption sites are facet-dependent. Exposed facets also determine the reaction kinetics of surface-bound pNPP mainly by regulating the Lewis acidity of the surface Fe(III) atoms. These findings underline the important roles of facets in determining the reactivity of naturally occurring metal-based nanoparticles toward environmental contaminants and may shed light on the development of nanomaterial-based remediation strategies.

Low-Molecular-Weight Organic Acid Complexation Affects Antimony(III) Adsorption by Granular Ferric Hydroxide.

Antimony(III) mobility in natural aquatic environments is generally enhanced by dissolved organic matter. Tartaric acid is often used to form complexes with and stabilize dissolved Sb(III) in adsorption studies. However, competition between such low-molecular-weight organic acid complexation and adsorption of Sb(III) has received little attention, which prompted us to measure Sb(III) adsorption by iron oxyhydroxide adsorbents commonly used in water treatment plants. Sb K-edge X-ray absorption fine structure (EXAFS) spectra gave Sb-O and Sb-Fe distances and coordinations compatible with a bidentate binuclear inner-sphere complex with trigonal Sb(O,OH)3 polyhedra sharing corners with Fe(O,OH)6 octahedra and a bidentate mononuclear inner-sphere complex but with Sb(O,OH)4 tetrahedra at alkaline pH. Experimental batch titration data were fitted using the charge-distribution multisite surface complexation (CD-MUSIC) model, constrained by the EXAFS molecular level information and taking competitive effects by the organic ligand into consideration. The proportion adsorbed at acid to neutral pH decreased as the Sb(III) concentration increased. The CD-MUSIC adsorption model indicates that this was solely caused by strong competition from tartrate complexation in solution, which leads to adsorption constants higher than those derived without taking this competition into account. The adsorption model results allow for calculating a pe-pH predominance diagram using the USGS PhreePlot code. The study provides consistent surface complexation stability constants, allowing the new database to be used also to reliably model adsorption of toxic oxyanions in anoxic aqueous environments: for example, to accurately simulate competition between Sb(III) and As(III).

A review of arsenic interfacial geochemistry in groundwater and the role of organic matter.

Recent discoveries on arsenic (As) biogeochemistry in aquifer-sediment system have strongly improved our understanding of As enrichment mechanisms in groundwater. We summarize here the research results since 2015 focusing on the As interfacial geochemistry including As speciation, transformation, and mobilization. We discuss the chemical extraction and speciation of As in environmental matrices, followed by As redox change and (im)mobilization in typical minerals and aquifer system. Then, the microbial-assisted reductive dissolution of Fe (hydr)oxides and As transformation and liberation are summarized from the aspects of bacterial isolates, microbial community and gene analysis by comparing As rich groundwater cases worldwide. Finally, the potential effect of organic matter on As interfacial geochemistry are addressed in the aspects of chemical interactions and microbial respiring activities for Fe and As reductive release.

Simultaneous removal of arsenic and antimony from mining wastewater using granular TiO2: Batch and field column studies.

Coexisting arsenic (As) and antimony (Sb) in mining wastewater is a common and great concern. On-site simultaneous removal of As and Sb from mining wastewater was achieved by using a reusable granular TiO2 column in this study. To evaluate the accuracy of the scale-up procedure, As and Sb adsorption from wastewater was studied in both large (600g TiO2) and small columns (12g TiO2) based on the proportional diffusivity rapid small-scale column tests (PD-RSSCTs) design. The comparable As and Sb breakthrough curves obtained from small and large columns confirmed the accuracy of the PD-RSSCT theory in the design of large-scale columns. Meanwhile, the consistent As and Sb adsorption results from batch and column experiments suggested that TiO2 adsorption for As and Sb can be predicted from bench-scale tests. Charge distribution multi-site complexation (CD-MUSIC) and one-dimensional transport modeling integrated in the PHREEQC program were performed to study the adsorption behaviors of As and Sb on the TiO2 surface. Coexisting ions, such as Ca2+, Mg2+, and Si4+, play an important role in As and Sb adsorption, and the breakthrough curves were well simulated after considering the compound ion effects. The results from this study highlight the surface reactions of As and Sb on TiO2 and provide a practical way for on-site remediation of industrial wastewater.

Molecular Insights into Glyphosate Adsorption to Goethite Gained from ATR-FTIR, Two-Dimensional Correlation Spectroscopy, and DFT Study.

Glyphosate (PMG) complexation on iron (hydr)oxides impacts its fate and transport in the environment. To decipher the molecular-level interfacial configuration and reaction mechanism of PMG on iron (hydr)oxides, the PMG protonation process, which influences the chemical and physical properties of PMG, was first determined using ATR-FTIR spectroscopy. The FTIR results reveal that the deprotonation occurs at carboxylate oxygen when pKa1< pH < pKa2, at phosphonate oxygen when pKa2< pH < pKa3, and at amino nitrogen when pH > pKa3. PMG complexation on goethite was investigated using in situ flow-cell ATR-FTIR, two-dimensional correlation spectroscopy (2D-COS), and density functional theory (DFT) calculations. The results indicate that the phosphonate group on PMG interacts with goethite to form inner-sphere complexes with multiple configurations depending on pH: binuclear bidentate (BB) and mononuclear bidentate (MB) without proton under acidic conditions (pH 5), mononuclear monodentate (MM) with proton and BB without proton at pH 6-8, and MM without proton under alkaline conditions (pH 9). Phosphate competition significantly impacted the PMG adsorption capacity and its interfacial configurations. As a result, the stability of the adsorbed PMG was impaired, as evidenced by its elevated leachability. These results improve our understanding of PMG-mineral interactions at the molecular level and have significant implications for risk assessment for PMG and structural analog pollutants.

Competing Interactions of As Adsorption and Fe(III) Polymerization during Ferric Coprecipitation Treatment.

This study revealed the effect of As on the formation and dissolution of iron (hydr)oxides and its further impact on the As removal efficacy of FeCl3 treatment. Adding 6.7 mg/L FeCl3 into 325 µg/L As solution (coprecipitation) resulted in more As removal (99% As(V) and 75% As(III)) at 2 min than adding As into aged FeCl3 solution (preaged, 52-87% As(V) and 7-42% As(III)) at pH 7. However, soluble As gradually increased in the coprecipitation system and decreased in the preaged system to give similar concentrations during 800 h aging. The particle size of the iron (hydr)oxides increased more slowly in the coprecipitation than in the preaged systems. These results suggest the rapid adsorption of As on Fe polymer during the initial polymerization process, which delays the growth of iron (hydr)oxides. Thermodynamically, quantum chemical calculations implied that iron ions adsorption on iron (hydr)oxide polymer was more stable than As adsorption, which is the main driving force for the As release during aging process. This study improved our understanding of the kinetic and thermodynamic processes of As adsorption and iron (hydr)oxide precipitation in the coprecipitation treatment of As, and the potential for As release during aging of sludge generated in the treatment.