Halide Concentration Research Articles

Chemometrics and elemental mapping by portable LIBS to identify the impact of volcanogenic and non-volcanogenic degradation sources on the mural paintings of Pompeii

Crystallization of soluble salts is a common degradation phenomenon that threatens the mural paintings of Pompeii. There are many elements that contribute to the crystallization of salts on the walls of this archaeological site. Notably, the leachates of the pyroclastic materials ejected in 79 AD by Mount Vesuvius and local groundwater, rich in ions from the erosion of volcanic rocks. Both sources could contribute to increase the concentration of halides (fluorides and chlorides) and other salts in these walls. The distribution of volcanogenic salts and their impact on the conservation of Pompeian mural paintings have however not yet been fully disclosed. In this work, an analytical methodology useful to determine the impact of the main sources of degradation affecting the mural paintings of Pompeii is presented. This methodology combines the creation of qualitative distribution maps of the halogens (CaF and CaCl) and related alkali metals (Na and K) by portable Laser Induced Breakdown Spectroscopy (LIBS) and a subsequent Principal Component Analysis of these data. Such maps, together with the in-situ identification of sulfate salts by portable Raman spectroscopy, provided information about the migration and distribution of volcanogenic halides and the influence of ions coming from additional sources (marine aerosol and modern consolidation mortars). Additionally, the thermodynamic modeling developed using the experimentally determined ionic content of Pompeian rain- and groundwater allowed to determine their specific role in the formation of soluble salts in the mural paintings of Pompeii.

Study of the Stability of Citrate Capped AgNPs in Several Environmental Water Matrices by Asymmetrical Flow Field Flow Fractionation.

Asymmetrical flow field-flow fractionation (AF4) coupled to UV-Vis and dynamic light scattering (DLS) detectors in series, was tested for stability studies of dispersions of citrate-capped silver nanoparticles (AgNPs) in several water matrices. The main goal is to provide knowledge to understand their possible behavior in the environment for short times since mixturing (up to 180 min). Ultrapure (UPW), bottled (BW1, BW2), tap (TW), transitional (TrW) and sea water (SW) matrices were assayed. Observations were compatible with the aggregation of AgNPs, a change in the plasmon band and a size growth with time were done. Fractograms showed different evolution fingerprints in the function of the waters and batches. The aggregation rate order was BW2, SW, TrW, BW1 and TW, being BW2 the lowest and TW the highest. NP aggregation can be induced by increasing the salt concentration of the medium, however transitional and sea waters did not follow the rule. Both matrices presented a lower aggregation rate in comparison with other aqueous matrices with much lower ionic strength (BW1 and TW), which can be explained by the potential presence of dissolved organic matter and/or the high concentration of halides providing their stabilization and passivation, respectively. AF4 provides relevant information with respect to static DLS and UV-Vis Spectroscopy showing that at least two populations of aggregates with different sizes between them, depending on both, the mixture time for a given matrix and type of water matrix for the same time.

Non-equilibrium solvent extraction in milliflow reactors: Precious and base metal separations with undiluted ionic liquids

Milliflow devices operating under slug flow (Taylor-flow) conditions provide an efficient mass transfer, a highly uniform droplet morphology and a narrow residence time distribution i.e. characteristics which are excellent for the performance of reactions under kinetic control. Milliflow devices have also been proposed in combination with ionic liquids, due to their ability to intensify the solvent use of these rather expensive and viscous liquids. In present research, the solvent extraction separation of a mixture of Au(III), Pd(II), Cu(II) and Fe(III) was studied using the chloride and bromide forms of the undiluted quaternary ammonium ionic liquid Aliquat 336 in a slug flow reactor channel with an internal diameter of 1.0 mm. The extraction of Au(III) and Pd(II) was found to be faster than that of Cu(II) and Fe(III), allowing the precious/base metal separation to be improved by modification of the contact time between both phases. An apparent correlation between the observed extraction rates and the equilibrium distribution ratio D was found. The most significant separation improvement was achieved at those conditions where the equilibrium separation was best i.e. low halide and metal concentrations and low organic-to-aqueous flow rate ratios. At a residence time of 25 s, quantitative Au(III) and Pd(II) recovery was achieved and decontamination factors increased by a factor up to 2, which corresponds to an increase in product purity of up to 14%. Upon substituting the chloride system for a bromide extraction medium, similar observations were made, except for a reversed Cu(II)/Fe(III) selectivity. Experiments were also conducted on the separation of Pt(IV), Pd(II) and Rh(III), where a reduced Rh(III) extraction rate was observed, allowing to suppress its co-extraction by up to 20%. A hydrodynamic analysis of the obtained flow regime of the ionic liquids revealed a stable and uniform slug flow characterized by a decreasing plug length and width with increasing flow rates. A comparison of the applied and observed phase ratio revealed a stagnant ionic liquid excess (i.e. hold-up) inside the reactor of up to 40% which effectively reduced the reactor diameter and consequently plug residence time.

Halogen Radicals Contribute to the Halogenation and Degradation of Chemical Additives Used in Hydraulic Fracturing.

In hydraulic fracturing fluids, the oxidant persulfate is used to generate sulfate radical to break down polymer-based gels. However, sulfate radical may be scavenged by high concentrations of halides in hydraulic fracturing fluids, producing halogen radicals (e.g., Cl•, Cl2•-, Br•, Br2•-, and BrCl•-). In this study, we investigated how halogen radicals alter the mechanisms and kinetics of the degradation of organic chemicals in hydraulic fracturing fluids. Using a radical scavenger (i.e., isopropanol), we determined that halogenated products of additives such as cinnamaldehyde (i.e., α-chlorocinnamaldehyde and α-bromocinnamaldehyde) and citrate (i.e., trihalomethanes) were generated via a pathway involving halogen radicals. We next investigated the impact of halogen radicals on cinnamaldehyde degradation rates. The conversion of sulfate radicals to halogen radicals may result in selective degradation of organic compounds. Surprisingly, we found that the addition of halides to convert sulfate radicals to halogen radicals did not result in selective degradation of cinnamaldehyde over other compounds (i.e., benzoate and guar), which may challenge the application of radical selectivity experiments to more complex molecules. Overall, we find that halogen radicals, known to react in advanced oxidative treatment and sunlight photochemistry, also contribute to the unintended degradation and halogenation of additives in hydraulic fracturing fluids.

Direct dynamics simulations on the atomic mechanisms of 4O+ + CH3I reaction

The reactions of oxygen radical cation O+ with haloalkanes are of importance in gas phase ion chemistry, but the studies on reactive patterns and dynamics are quite limited. In this work, the direct dynamics simulations have been carried out at the B3LYP/ECP/d level of theory for 4O+ + CH3I reaction at Ecoll = 4.5 eV, and the results are compared with the available experiments. The properties of stationary points on the potential energy surface for 4O+ + CH3I reaction have been characterized and supplemented in terms of our simulations. Variety of atomic reaction mechanisms are revealed and are found to be energetically accessible at high collision energy, including charge transfer, dissociative charge transfer, proton transfer, substitution, and complex rearrangement, which exclusively proceed by direct mechanism due to the high collision energy. Our work has confirmed the existence of the charge transfer product CH3I+, which is highly exothermic. The major product CH3+ can be produced in concert with IO molecule, besides the dissociative charge transfer process of CH3I+. Similarly, including the possible dissociation of CH3I+, product I+ can be formed by substitution reaction. Some trace products, i.e., CH2I+, H2CO+, and CH3O+, are also found in our simulations. This work is expected to enrich our understanding of the significant atmospheric concentrations of these methyl halides and their anthropogenic origins.

New Perception to Proto History Burial Site in Andarawewa: An Archaeological and Geochemical Prospection

The megalithic burial site at Galgamuwa Andarawewa is situated at Anamaduwa Secretariat Division in the North Western Province, Sri Lanka. It is evident that 2500 years ago the proto history people had settled in this region. For burying of bodies, they have constructed different types of burials in several places in this region. Thus, to examine the geochemical prospection soil samples from the context (n=12), the glass bead samples from the furnace (n=3) and slag (n=2) were analyzed using X-Ray Fluorescence (XRF) for 22 major and trace elements. For the archaeological prospection, new findings of proto-history burials were found in the excavation carried out at Andarawewa and also many archaeological evidences were found through the field survey and excavations such as beads, inscriptions, pots and shard and chisels. The elemental values of the slag show that, Pb (470-483 mg/Kg) and Cu (855-1083 mg/Kg) are very much higher than Upper Continental Crustal Values. The white part contains higher Pb and Cu than the dark part of the slag. The concentrations of halides F, Br and I are almost similar in the white (glass) part and dark (slag) part. The Pb, Cu and as in the glass beads of the Andrawewa furnace shows that they range between 390-2920, 275-1411 and 12-127 mg/Kg respectively. However, the Fe and Ti concentrations are much lower than in the contexts though P2O5 is higher in the bead samples. The soil samples from the contexts of the area does not show high values for almost all the measured elements. Thus, indicating that the soils are local while the beads may have been prepared with sands brought from other areas. The carbon dating has dated that this burial belongs to the period from 500- 507 B.C.

Organic electrochemical transistor on paper for the detection of halide anions in biological analytes

This report describes an open-air, screen-printed organic electrochemical transistor (OECT) fabricated on a paper substrate for the determination of halide ion concentrations within ranges relevant for human disease diagnosis. Chloride ions (Cl−) owing to their prevalence in biochemistry were specifically evaluated and the OECT’s efficacy with regards to measuring biologically relevant Cl− concentrations in the presence of multiple cationic and anionic interference species was studied. Sensor response was evaluated using both bench-top measurements as well as with hybrid data processing and notification circuitry assembled on the same flexible paper substrate as the OECT. To simplify the measurement process, a current-to-voltage converter was screen-printed in series with the OECT channel to facilitate voltage measurements in direct correlation with the drain current modulations. The bio-electronic conductive polymer poly(3,4-ethylenedioxythiophene) poly(styrene sulphonate) (PEDOT:PSS) was utilized as the transistor channel and silver (Ag) was used as the halide-selective gate electrode. Finally, the paper OECT and the on-board hybrid circuitry were powered using Zn-MnO2-ZnCl2 based printed paper cells and the biosensor’s suitability towards distinguishing between Cl− concentrations clinically associated with a diagnosis of cystic fibrosis was evaluated as a proof of concept. This work demonstrates a simple biosensing system working in the faradaic mode of operation without the implementation of selective ionophore films and incorporates aspects of recyclability, biodegradability and eco-friendliness.

Kinetic control of hierarchical growth

Nanomaterials Sequential seeding of nanocrystals can be used to control and develop complex shapes during growth. Smith et al. explored the effects of limiting adatom addition versus diffusion for gold or palladium grown on gold seeds. Fast growth conditions promote branched nanocrystals along the directions. The addition of hydrochloric acid lowered the pH and increased the halide concentration, slowing the rate of metal precursor reduction. Fast growth promoted concave shapes, whereas slower growth favored convex ones. By using the production of one growth cycle as the seed for the next one, 85 distinct hierarchical shapes were grown. ACS Nano 10.1021/acsnano.0c07384 (2020).

Removal of disinfection by-product precursors by ion exchange resins

The removal of dissolved organic carbon (DOC) is a key factor in the control of disinfection by-product (DBP) formation in drinking water. Ion exchange process deals with the removal of naturally negatively charged organic matter. A fluidized bed column test has been chosen to test in parallel the efficiency of 4 different anionic exchange resins (Purolite PPA860S, Dowex TAN-1, Amberlite IRA-958 and IRA-410) in terms of DOC fraction removal and related DBP formation reduction. IRA-410 was shown to be the best performing resin in terms of DOC and DBP formation potential reduction followed by PPA860S. These resins removed respectively 41 and 37 % of DOC, with humic substances as the main target of the two resins (68 and 72 % reduction, respectively, based on size exclusion chromatography with an organic carbon detector). The UV absorbance was reduced in a higher proportion than the DOC demonstrating a preference of the resins for the relatively hydrophobic compounds. The reduction in trihalomethane and haloacetic acid formation was higher than the DOC removal for IRA-410 and PPA860S (53 and 59 %, respectively); whereas IRA-958 on the other hand showed a lower reduction in DBP formation potential than its DOC removal. All the resins showed a much higher reduction of iodinated trihalomethanes formation potential (66–96% reduction compared to raw water) due to the removals of iodide in addition of organic precursors. However, in a context of increasing halide concentrations, the different resins showed a reduction of their efficiency to control the formation of DBPs.

Removal of the precursors of regulated DBPs and TOX from surface waters and wastewater effluents using mixed anion exchange resins

Both organic and inorganic precursors play important roles in the formation and speciation of disinfection by-products (DBPs). This study aimed to investigate the efficacy of three different anion exchange resins for removing both organic and inorganic DBP precursors simultaneously in a single treatment system. Resins in the single (Purolite®-Br, MIEX®-Br, and MIEX®-Gold) and mixed (Purolite®-Br with MIEX®-Gold and MIEX®-Br with MIEX®-Gold) application modes were tested and compared for the removal of dissolved organic carbon (DOC), bromide (Br−), and iodide (I−) from a raw source water and a treated wastewater effluent. Uniform formation condition (UFC) tests were conducted to measure the concentrations of trihalomethanes (THM4), haloacetic acids (HAA9), haloacetonitriles (HAN6), and total organic halides (TOX): total organic chlorine (TOCl), total organic bromine (TOBr), and total organic iodine (TOI) before and after the anion exchange resin treatments. The anion exchange treatment substantially lowered the DOC, UV254 absorbing matter, dissolved nitrogen (DN), Br−, and I−. Consequently, the formation of THM4, HAA9, HAN6, and TOX in the examined chlorinated water samples were reduced significantly. The maximum reduction in THM4 and TOX (66–69% and 61%, respectively) from wastewater effluent was achieved by the mixed resin system, which also reduced the THM4 and TOX by 77% and 77%, respectively, from raw source water. Overall, mixed resin systems (a DOC-selective and a Br-selective resin) resulted in lower amounts of THM4 and HAA9 formation during subsequent chlorination with lower bromine incorporation as compared to single resin systems. Furthermore, they exhibited lower TOBr formation, while TOI formation was not detected.

Degradation of Acetaminophen via UVA-induced advanced oxidation processes (AOPs). Involvement of different radical species: HO[rad], SO4[rad]− and HO2[rad]/O2[rad

In this work, UVA radiation that is part of solar light is taken as the irradiation source and radicals (HO, SO4− and HO2/O2−) are generated through activation of hydrogen peroxide (H2O2), sodium persulfate (Na2S2O8) and Bismuth catalyst (BiOCl), respectively. The distinguished performance in removing acetaminophen (ACTP), a model pharmaceutical pollutant, by these three radicals was compared for the first time. Effect of pH, halide ions concentration and interfacial mechanism have been investigated in detail. Interestingly, results show that heterogeneous UVA/BiOCl process has higher degradation efficiency than homogeneous UVA/H2O2 and UVA/Na2S2O8 systems whatever the solution’s pH. To explain these results, second order reaction rate constant (kradical, ACTP) have been determined with laser flash photolysis (LFP) or radical scavenging experiments. The strongly interfacial-depended HO2/O2− radicals have the lowest second order rate constant with ACTP but highest steady state concentration. BiOCl is much easier activated by UVA, and outstanding ACTP mineralization can be achieved. Combination of BiOCl and Na2S2O8 exhibits synergistic effects rather than antagonism effects with H2O2. This study highlights the relative effective utilization of solar light through interfacial directed BiOCl photocatalysis and its synergistic effects with traditional oxidants.

Performance analysis of an efficient and stable perovskite solar cell and a comparative study of incorporating metal oxide transport layers

As poor stability is the primary constraint for the commercialization of perovskite solar cells, improving stability has been the primary focus of recent research works regarding solar cells that make use of perovskite materials. Different metal oxide transport layers are being used with the aim of fabricating stable perovskite solar cells. A stable and efficient solar cell with both metal oxide transport layers (ZnO and N i O X ) and a perovskite (methyl ammonium lead iodide) absorber layer is simulated in this work, and a comparison of performance parameters is made with other transport layers from the literature. The issue of optimization regarding the thickness of the absorber layer and the doping concentration in the absorber and transport layers has been addressed, and the effect of defect concentration at the interface has been investigated. Optimum performance is achieved with an absorber layer of thickness 800 nm. Linear grading is also introduced in the absorber layer by varying the concentration of different halides, which increases the efficiency by approximately 8% owing to the increase in the short circuit current density.

Predicting Residual Adsorbable Organic Halides Concentrations in Industrial Wastewater Using Typical Wastewater Parameters

The aim of this study was to predict the residual adsorbable organic halides (AOX) concentration in an industrial wastewater using conventional, easy-to-measure wastewater parameters. In a pilot test unit, the wastewater was subjected to ozonation at various intensities, resulting in an AOX-removal and hence varying AOX concentrations. In first instance, the parameters used for modeling were selected using Pearson and Spearman correlations. Secondly, multiple linear regression (MLR) was used as a modeling tool to predict both the soluble and total AOX concentration in wastewater samples. To prevent overfitting, a 10-fold cross-validation was carried out. It was found that both the soluble and the total AOX concentration can be predicted using typical wastewater parameters. The measured parameters were pH, chloride concentration, Water-Soluble Organic Carbon concentration (WSOC), UV-VIS spectrum, turbidity, and Solids Removable by Filtration (SRF). Out of these parameters, the following parameters were found to be significant for prediction of the total AOX concentration: turbidity; SRF; UV-VIS absorbance at 200; 227, and 250 nm; and pH. UV-VIS absorbance at 200 and 227 nm and turbidity of the wastewater were found to contribute significantly to the final model. For the soluble AOX concentration, the significant parameters were turbidity; SRF; absorbance at 200, 227, and 250 nm; pH, and chloride concentration. Here, UV-VIS absorbance at 200 and 227 nm were found to contribute significantly to the final model. The obtained final models had an adjusted R2 of 0.921 and 0.916 for the total and soluble AOX, respectively. As a result of the obtained models, both AOX concentrations can be predicted using parameters that are easier to determine. This allows for a significant reduction in wastewater sampling and analysis time and offers the opportunity to optimize the ozone dosing in the wastewater treatment process in the future.

Enhanced colloidal stability of perovskite quantum dots via split-ligand re-precipitation for efficient bi-functional interlayer in photovoltaic application

A split-ligand mediated re-precipitation (Split-LMRP) technique for colloidal perovskite quantum dots (QDs) was designed by separately dissolving rich oleic acid (OA) and amine ligands in the synthesis process. OA was used to control the polarity of the nucleation environment and was simultaneously employed as a stabilizer. The Split-LMRP technique allowed purification via the precipitation of QDs from a colloidal solution. The fabrication process is performed under ambient conditions, and the resulting CH3NH3PbX3 (X=Br, I) QDs exhibited strong photoluminescence (PL) emission with a maximum PL quantum yield of 91.5%. The size of the resulting perovskite QDs is tuned in the range of 2–5nm by varying the ligand concentration and type of halide. We also investigated the charge-transport properties of the synthesized QDs using space-charge-limited current analysis and confirmed stable charge carrier mobility even when the QDs solution was spin-coated on a hydrophilic poly (3,4-ethylenedioxythiophene) polystyrene sulfonate film. Furthermore, the enhanced stability of CH3NH3PbX3 (X=Br, I) QDs improved the power conversion efficiency by the uniform surface passivation of the perovskite active layer which induces efficient exciton generation and charge transport.

Tantalum Recycling by Solvent Extraction: Chloride Is Better than Fluoride

The recycling of tantalum (Ta) is becoming increasingly important due to the criticality of its supply from a conflict mineral. It is used extensively in modern electronics, such as in capacitors, and so electronic waste is a potentially valuable secondary source of this metal. However, the recycling of Ta is difficult, not least because of the challenges of its leaching and subsequent separation from other metals. In this work, we show that Ta(V) halides, such as TaCl5 and TaF5, which can potentially be accessed from Ta metal upon acid halide leaching, can be recovered by solvent extraction using a simple primary amide reagent. The need for high halide concentrations in the aqueous phase implies the formation of the hexahalide salts [TaX6]− (X = F, Cl) and that an anion-swing mechanism operates. While extraction of the fluorides is poor (up to 45%), excellent extraction under chloride conditions is found (>99%) and presents an alternative route to Ta recycling.

Determining P, S, Br, and I content in uranium by triple quadrupole inductively coupled plasma mass spectrometry

The trace impurities of a uranium ore concentrate (UOC) can be examined to determine mine source, methods of production, and quality. This study presents a method to determine the concentration of halides and main group elements, specifically P, S, Br and I, utilizing triple quadrupole inductively coupled plasma–mass spectrometry. These analytes were measured in a uranium matrix to simulate a UOC sample. The concentrations determined with this method showed agreement with known values. Solutions with and without uranium were compared. A UOC certified reference material, CUP-2, was analyzed to further demonstrate the effectiveness of the method.

Impact of Perovskite Composition on Film Formation Quality and Photophysical Properties for Flexible Perovskite Solar Cells.

In recent years, flexible perovskite solar cells have drawn tremendous attention in the field of wearable devices, and optimization of perovskite composition plays an important role in improving film quality and photophysical properties. At present, some researchers have only studied A-site organic cations mixing or X-site halide anions mixing in the ABX3 structure of perovskite, but there are few reports on co-mixing of A-site and X-site ions in flexible perovskite solar cells. In this paper, we mainly try to study the effects of different concentrations of mixed formamidine methylamine halide (FAxMA1-xBrxClyI1-x-y) precursor solutions on the quality and photophysical properties of perovskite films under low temperature process. We conclude that the film quality and photophysical properties reached the best results when the optimized precursor solution concentration was 60:6:6. The investigation on composition optimization in this experiment laid the foundation for the improvement of the performance of flexible perovskite solar cells. We also use the results of this experiment to prepare flexible perovskite solar cells based on carbon electrodes, which are expected to be applied in other flexible optoelectronic or electro-optical devices.

Elucidating sulfate radical-mediated disinfection profiles and mechanisms of Escherichia coli and Enterococcus faecalis in municipal wastewater

Practical applications of disinfection technologies for engineered waters require an in‒depth understanding of disinfection profiles and mechanisms of pathogenic bacteria in a complex matrix. This study investigated the inactivation of E. coli and E. faecalis by SO4•−, an emerging advanced disinfectant, in ultrapure water (UPW) and wastewater effluent (WE). Based on the bacterial inactivation kinetics in UPW in a zerovalent iron/peroxydisulfate system, the second order rate constants (k) for SO4•− reacting with E. coli and E. faecalis were measured to be (1.39 ± 0.1) × 109 M−1 s−1 and (6.71 ± 0.1) × 109 M−1 s−1, respectively. The morphological images of both bacteria by the scanning electron microscope indicated that SO4•− initiates oxidative reactions on the wall/membranes, causing their irreversible damage, ultimately affecting membrane permeability and physiological functions. To profile the inactivation kinetics of two strains of bacteria in WE matrix, a mechanistic process‒based model with the obtained k values was developed. Sensitivity and uncertainty analyses indicated that the key parameters for the model predictions were the concentrations of halide ions (i.e., Br− and Cl−) in WE and their k values reacting with SO4•− accounting for >80% of uncertainty or variance expected in predicted bacterial inactivation. This model allows precise estimation of required disinfectant dose even in complex water matrices, shedding lights on the extension of application of SO4•−‒based technology in wastewater treatments.

Role of Solid-State Miscibility during Anion Exchange in Cesium Lead Halide Nanocrystals Probed by Single-Particle Fluorescence.

In this Letter, we used fluorescence microscopy to image the reversible transformation of individual CsPbCl3 nanocrystals to CsPbBr3, which enables us to quantify heterogeneity in reactivity among hundreds of nanocrystals prepared within the same batch. We observed a wide distribution of waiting times for individual nanocrystals to react as has been seen previously for cation exchange and ion intercalation. However, a significant difference for this reaction is that the switching times for changes in fluorescence intensity are dependent on the concentration of substitutional halide ions in solution (i.e., Br- or Cl-). On the basis of the high solid-state miscibility between CsPbCl3 and CsPbBr3, we develop a model in which the activation energy for anion exchange depends on the density of exchanged ions in the nanocrystal. The heterogeneity in reaction kinetics observed among individual nanocrystals limits the compositional uniformity that can be achieved in luminescent CsPbCl3-xBrx nanocrystals prepared by anion exchange.

Formation of haloacetic acids from different organic precursors in swimming pool water during chlorination

Haloacetic acids (HAAs) were reported to be the most abundant category of DBPs in swimming pool water. In this study, the formation of HAAs from different organic precursors in swimming pool water, including UV filters, human body fluids, and natural organic matter (NOM), during chlorination was examined, and the effects of chlorine dose and halide concentrations on the formation of HAAs were evaluated. The results show that the total HAA yields from benzophenone-3 (BP-3) and Suwannee River humic acid (SRHA) were the highest among the nine organic precursors, and the yields of dichloroacetic acid and bromochloroacetic acid were higher than that of the other HAA species. In all the chlorinated samples of different organic precursors, longer chlorination time enhanced HAA formation. Both chlorine dose and bromide concentration significantly affected the formation of HAAs from BP-3 and SRHA during chlorination. With the increasing chlorine dose, the total HAA yields from SRHA and BP-3 significantly increased. Besides, the proportion of trihaloacetic acids (THAAs) rose while that of dihaloacetic acids (DHAAs) and monohaloacetic acids (MHAAs) declined with the increasing chlorine dose. With the increasing bromide concentration, HAA formation from SRHA increased while that of BP-3 decreased. The bromine incorporation factor (BIF) of the formed MHAAs, DHAAs and THAAs from SRHA and BP-3 both increased with the increasing bromide concentration in the following order: BIFDHAAs > BIFTHAAs > BIFMHAAs, indicating that bromine was easier to be incorporated into DHAAs rather than MHAAs or THAAs. Moreover, bromide promoted the formation of Br-HAAs.