Activation of peroxymonosulfate by Fe,N co-doped walnut shell biochar for the degradation of sulfamethoxazole: Performance and mechanisms.

Fe and N co-doped walnut shell biochar (Fe,N-BC) was prepared through a one-pot pyrolysis procedure by using walnut shells as feedstocks, melamine as the N source, and iron (III) chloride as the Fe source. Moreover, pristine biochar (BC), nitrogen-doped biochar (N-BC), and α-Fe2O3-BC were synthesized as controls. All the prepared materials were characterized by different techniques and were used for the activation of peroxymonosulfate (PMS) for the degradation of sulfamethoxazole (SMX). A very high degradation rate for SMX (10 mg/L) was achieved with Fe,N-BC/PMS (0.5 min-1), which was higher than those for BC/PMS (0.026 min-1), N-BC/PMS (0.038 min-1), and α-Fe2O3-BC/PMS (0.33 min-1) under the same conditions. This is mainly due to the formation of Fe3C and iron oxides, which are very reactive for the activation of PMS. In the next step, Fe,N-BC was employed for the formation of a composite membrane structure by a liquid-induced phase inversion process. The synthesized ultrafiltration membrane not only exhibited high separation performance for humic acid sodium salt (HA, 98%) but also exhibited improved self-cleaning properties when applied for rhodamine B (RhB) filtration combined with a PMS solution cleaning procedure. Scavenging experiments revealed that 1O2 was the predominant species responsible for the degradation of SMX. The transformation products of SMX and possible degradation pathways were also identified. Furthermore, the toxicity assessment revealed that the overall toxicity of the intermediate was lower than that of SMX.

A review on co-metabolic degradation of organic micropollutants during anaerobic digestion: Linkages between functional groups and digestion stages.

The emerging presence of organic micropollutants (OMPs) in water bodies produced by human activities is a source of growing concern due to their environmental and health issues. Biodegradation is a widely employed treatment method for OMPs in wastewater owing to its high efficiency and low operational cost. Compared to aerobic degradation, anaerobic degradation has numerous advantages, including energy efficiency and superior performance for certain recalcitrant compounds. Nonetheless, the low influent concentrations of OMPs in wastewater treatment plants (WWTPs) and their toxicity make it difficult to support the growth of microorganisms. Therefore, co-metabolism is a promising mechanism for OMP biodegradation in which co-substrates are added as carbon and energy sources and stimulate increased metabolic activity. Functional microorganisms and enzymes exhibit significant variations at each stage of anaerobic digestion affecting the environment for the degradation of OMPs with different structural properties, as these factors substantially influence OMPs' biodegradability and transformation pathways. However, there is a paucity of literature reviews that explicate the correlations between OMPs' chemical structure and specific metabolic conditions. This study provides a comprehensive review of the co-metabolic processes which are favored by each stage of anaerobic digestion and attempts to link various functional groups to their favorable degradation pathways. Furthermore, potential co-metabolic processes and strategies that can enhance co-digestion are also identified, providing directions for future research.

Revolutionizing sanitation: Valorizing fecal slags through co-digesting food waste at high-solid content and dosing metallic nanomaterials for anaerobic digestion stability.

To achieve the UN Sustainable Development Goals (SDGs) and the China Toilet Revolution on a global scale, it is crucial to implement a decentralized sanitation management system in developing countries. Fecal slags (FS) generated from septic tanks of toilets pose a challenge for remote villages. This study sought to resourcefully utilize FS through co-digesting with food waste (FW) under high-solid anaerobic co-digestion (HSAD). Besides, two metallic nanomaterials, nano-zerovalent iron (nZVI) and magnetite (Fe3O4), were employed to demonstrate the practical improvement of HSAD. The results showed that nZVI-dosed digesters produced the highest cumulative methane of 295.72 mL/gVS, 371.36 mL/gVS, 360.53 mL/gVS and 296.64 mL/gVS in 10%, 15%, 20% and 25% TS content, respectively, which was 1.15, 1.22, 1.16, 1.12 times higher than Fe3O4 dosed digesters. This increment could be ascribed to the simultaneous production of H2 from Fe2+ release from nZVI and the enrichment of homoacetogen. Changes in carbon degradation and methanogenic pathways, which facilitated stability under high TS contents, were observed. At low solid digestion (10% TS), Syntrophomonas cooperated with Methanosarcina and Methanobacterium to metabolize butyrate and propionate. However, due to the buildup of total ammonia nitrogen and volatile fatty acids, acetoclastic methanogens were inhibited in the high-solid digesters (15%, 20% and 25% TS). Consequently, a more resilient and highly tolerant Syntrophaceticus, alongside hydrogenotrophic methanogens such as Methanoculleus and Methanobrevibacter, maintained stability in the harsh environment.

A walnut shell biochar-nano zero-valent iron composite membrane for the degradation of carbamazepine via persulfate activation.

In this study, novel walnut shell biochar-nano zero-valent iron nanocomposites (WSBC-nZVI) were synthesized using a combined pyrolysis/reduction process. WSBC-nZVI displayed a high removal efficiency (86 %) for carbamazepine (CBZ) compared with walnut shell biochar (70 %) and nano zero-valent iron (76 %) in the presence of persulfate (PS) (0.5 g/L catalyst, 10 mg/L CBZ, 1 mM persulfate). Subsequently, WSBC-nZVI was applied for the fabrication of the membrane using a phase inversion method. The membrane demonstrated an excellent removal efficiency of 91 % for CBZ in a dead-end system (2 mg/L CBZ, 1 mM persulfate). In addition, the effect of various operating conditions on the degradation efficiency in the membrane/persulfate system was investigated. The optimum pH was close to neutral, and an increase in CBZ concentration from 1 mg/L to 10 mg/L led to a drop in removal efficiency from 100 % to 24 %. The degradation mechanisms indicated that oxidative species, including 1O2, OH, SO4-, and O2-, all contribute to the degradation of CBZ, while the role of 1O2 is highlighted. The CBZ degradation products were also investigated, and the possible pathways and the predicted toxicity of intermediates were proposed. Furthermore, the practical use of the membrane was validated by the treatment of real wastewater.

Life cycle assessment of municipal biowaste management - a Czech case study.

As part of coming targets to transition to a sustainable society and actively set a circular economy, one of the EU objectives is to decrease the amount of municipal solid waste and initiate the separation of its organic fraction, i.e., biowaste. Consequently, the question of how to best manage biowaste at the municipal level is of high importance, and previous research has shown the strong influence of local factors on the most sustainable treatment option. Life Cycle Assessment is a valuable tool for comparison of waste management impacts and was used to assess environmental impacts of the current biowaste management in Prague and give insight for improvements. Different scenarios were created regarding EU and Czech biowaste targets for separated collection. Results show the significant influence of the source of energy that is substituted. Consequently, in the current situation of an energy mix highly based on fossil fuels, incineration is the most sustainable option in most impact categories. However, community composting was found to have a better potential to reduce ecotoxicity and resource use of minerals and metals. Furthermore, it could supply a significant proportion of the minerals need of the region while increasing the autonomy of the Czech Republic regarding mineral fertilisers. To meet targets of EU directives for separated collection of biowaste, a combination of anaerobic digestion, to avoid use of fossil fuels, and composting, to increase circular economy, is most likely the best option. The outputs of this project would be of great significance for municipalities.

Sustainability insights into the synthesis of engineered nanomaterials - Problem formulation and considerations.

Engineered nanomaterials (ENMs) have been introduced into the market for a wide range of applications. As per the literature review, the fabrication of new generations of ENMs is starting to comply with environmental, economic, and social criteria in addition to technical aspects to meet sustainability criteria. At this stage, identification of the appropriate criteria for the synthesis of ENMs is critical because the technologies already developed at the lab scales are being currently transferred to pilot and full scales. Hence, the development of scientific-based methodologies to identify, screen, and prioritize the involved criteria is highly necessary. In the present manuscript, a fuzzy-Delphi methodology is adopted to identify the main criteria and sub-criteria encompassing the sustainable fabrication of ENMs, and to explore the "degree of consensus" among the experts on the relative importance of the mentioned criteria. The "health and safety risks" respecting the equipment and the materials, solvent used, and availability of "green experts" were identified as the most critical criteria. Furthermore, although all the criteria were identified as being important, some criteria, such as "solvent" and "raw materials cost", raised a lower degree of consensus, indicating that various "degrees of uncertainties" still exist regarding the level of importance of the studied criteria.

Immobilization of photocatalytic materials for (waste)water treatment using 3D printing technology - advances and challenges.

Photocatalysis has been considered a promising technology for the elimination of a wide range of pollutants in water. Various types of photocatalysts (i.e., homojunction, heterojunction, dual Z-scheme photocatalyst) have been developed in recent years to address the drawbacks of conventional photocatalysts, such as the large energy band gap and rapid recombination rate of photogenerated electrons and holes. However, there are still challenges in the design of photocatalytic reactors that limit their wider application for real (waste)water treatment, such as difficulties in their recovery and reuse from treated (waste)waters. 3D printing technologies have been introduced very recently for the immobilization of materials in novel photocatalytic reactor designs. The present review aims to summarize and discuss the advances and challenges in the application of various 3D printing technologies (i.e., stereolithography, inkjet printing, and direct ink writing) for the fabrication of stable photocatalytic materials for (waste)water treatment purposes. Furthermore, the limitations in the implementation of these technologies to design future generations of photocatalytic reactors have been critically discussed, and recommendations for future studies have been presented.

Bifunctional g-C3N4/carbon nanotubes/WO3 ternary nanohybrids for photocatalytic energy and environmental applications.

Ternary nanohybrids based on mesoporous graphitic carbon nitride (g-C3N4) were synthesized and presented for developing stable and efficient Hydrogen (H2) production system. Based on photocatalytic activity, optimization was performed in three different stages to develop carbon nanotubes (CNTs) and WO3 loaded g-C3N4 (CWG-3). Initially, the effect of exfoliation was investigated, and a maximum specific surface area of 100.77 m2/g was achieved. 2D-2D interface between WO3 and g-C3N4 was targeted and achieved, to construct a highly efficient direct Z-scheme heterojunction. Optimized binary composite holds the enhanced activity of about 2.6 folds of H2 generation rates than the thermally exfoliated g-C3N4. Further, CNT loading towards binary composite in an optimized weight ratio enhances the activity by 6.86 folds than the pristine g-C3N4. Notably, optimized ternary nanohybrid generates 15,918 µmol h-1. g-1cat of molecular H2, under natural solar light irradiation with 5 vol% TEOA as a sacrificial agent. Constructive enhancements deliver remarkable H2 production and dye degradation activities. Results evident that, the same system can be useful for pilot-scale energy generation and other photocatalytic applications as well.

Water splitting by MnFe2O4/Na2CO3 reversible redox reactions.

Future energy systems must call upon clean and renewable sources capable of reducing associated CO2 emissions. The present research opens new perspectives for renewable energy-based hydrogen production by water splitting using metal oxide oxidation/reduction reactants. An earlier multicriteria assessment defined top priorities, with MnFe2O4/Na2CO3/H2O and Mn3O4/MnO/NaMnO2/H2O multistep redox cycles having the highest potential. The latter redox system was previously assessed and proven difficult to be conducted. The former redox system was hence experimentally investigated in the present research at the 0.5 to 250 g scale in isothermal thermogravimetry, an electrically heated furnace, and a concentrated solar reactor. Over 30 successive oxidation/reduction cycles were assessed, and the H2 production efficiencies exceeded 98 % for the coprecipitated reactant after these multiple cycles. Tentative economics using a coprecipitated reactant revealed that 120 cycles are needed to achieve a 1 € per kg H2 cost. Improving the cheaper ball-milled reactant could reduce costs by approximately 30 %. The initial results confirm that future research is important.

Producing hydrogen by catalytic steam reforming of methanol using non-noble metal catalysts.

Current energy systems have a significant environmental impact and contribute to the climate change. The future energy systems must call upon clean and renewable sources, capable of producing energy with low CO2 emission, hence partly decarbonizing the energy sector. Producing H2 by catalytic steam reforming of methanol (CSRM) is gaining interest for its specific applications in fuel cells, in a decentralized H2 production, or to locally boost the heat content of e.g. natural gas. Supported metal catalysts enhance the endothermic steam-driven methanol conversion. The paper discusses the CSRM manufactures and assesses 2 novel, cheap and efficient catalysts (Co/α-Al2O3 and MnFe2O4). The performance of the Co/α-Al2O3 catalyst is significantly superior to MnFe2O4. The methanol conversion exceeds 95% with high H2 yields (>2.5 mol H2/mol CH3OH) and low CO and CO2 by-product formation. The methanol reaction is very fast and a nearly constant product distribution is achieved for gas-catalyst contact times in excess of 0.3 s. The catalyst maintains its efficiency and selectivity for several days of reaction. The hydrogen productivity of the Co/α-Al2O3 is about 0.9 L H2 gcat-1 h-1., nearly a fourfold of the MnFe2O4 alternative. The different occurring reactions are combined in a kinetics analysis and demonstrate the high rate of reaction and the predicted product distribution. A catalytic sintered metal fleece reactor is finally developed, mostly in view of its integration with a solid oxide fuel cell (SOFC). The assessed CSRM system clearly merits further pilot plant research.

Changes in the microbiota during biological treatment of palm oil mill waste: A critical review.

Palm oil mill waste has a complex cellulosic structure, is rich in nutrients, and provides a habitat for diverse microbial communities. Current research focuses on how the microbiota and organic components interact during the degradation of this type of waste. Some recent studies have described the microbial communities present in different biodegradation processes of palm oil mill waste, identifying the dominant bacteria/fungi responsible for breaking down the cellulosic components. However, understanding the degradation process's mechanisms is vital to eliminating the need for further pretreatment of lignocellulosic compounds in the waste mixture and facilitating the commercialization of palm oil mill waste treatment technology. Thus, the present work aims to review microbial community dynamics via three biological treatment systems comprehensively: composting, vermicomposting, and dark fermentation, to understand how inspiration from nature can further enhance existing degradation processes. The information presented could be used as an umbrella to current research on biological treatment processes and specific research on the bioaugmentation of indigenous microbial consortia isolated during the biological degradation of palm oil mill waste.

A redox-based strategy to enhance propionic and butyric acid production during anaerobic fermentation.

This study investigated the selective production of volatile fatty acids (VFAs) during anaerobic mixed-culture fermentation. The experiment used chicken manure (CM) as a potential substrate to produce high added-value propionic acid and butyric acid under an alkaline environment. The conversion of CM into selective VFAs depends highly on operational conditions such as pH and redox balance. Therefore, the current experiment is designed to employ amino acid addition and develop a redox balance control method to control the final VFA profile. This study showed that 0.2-5.0 % valine and threonine addition successfully enhanced propionic acid and butyric acid production during alkaline fermentation and hence decreased the proportion of acetic acid from 83 % to approximately 47 %. The oxidation-reduction potential (ORP) and redox cofactor ratio (NADH/NAD+) were measured to support the selective VFA production mechanism. The results obtained in this study bring extra value to the valorization of CM within the circular economy concept for selective value-added VFA production.

Novel approach to ammonia recovery from anaerobic digestion via side-stream stripping at multiple pH levels.

Ammonia recovery from anaerobic digesters via side-stream stripping is a technique to recover nitrogen from manure wastes. This study demonstrated a novel approach to determining ammonia recovery to maintain total ammonia concentrations in the digester in the range of 1.7-2.1 gN/L. Increasing the pH during stripping from 8, 8.5 to 9.5 did not affect the stability of the digester. Methane yields of 60-80 mL/(gVS.d) and volatile fatty acid concentrations of 0-500 mg/L were reported throughout its operation. The low solubilisation increase upon recirculation of the digestate explained the lack of change in methane yields due to side-stream stripping. Increasing the pH during stripping also did not affect the digester's operating pH, which was attributed to the neutralising effect of biogas as stripping gas. Therefore, total ammonia concentrations in the digester can be controlled by determining the extent of ammonia recovery, and the pH during stripping can be increased without compromising the digester's stability.

Adsorption of acid fuchsine dye from wastewater by Mg-ferrite particles.

Adsorption is a widely applied waste water treatment technology, especially for removing micro-pollutants and dyes of industrial effluents. Over the past decade, adsorbing metal oxide micron- and nano-particles have been successfully developed and investigated as adsorbents. In the present research, Mg-ferrite adsorbent particles were synthesized and their properties were fully determined. The pore volume is 0.139 cm3/g. The BET analysis reveals a surface area of 94.4 m2/g. The porosity is of meso- and microporous nature. The adsorbent was used to adsorb acid fuchsine, an important industrial dye. The equilibrium adsorption capacity was 796.4 mg/g, with an adsorption yield of 78.7-82.0%. The adsorption kinetics can be adequately fitted by a pseudo-second-order model. The isotherms of both Langmuir and Freundlich are applicable. The stability, recovery and reuse of the ferrite particles were proven in multi-cycle experiments, and the adsorption activity decreased by less than 3% between the first and fifth cycle. Experimental and fitting results were finally used to design a batch adsorber to remove a given concentration of acid fuchsine from different volumes of wastewater.

ZnO/γ-Fe2O3/Bentonite: An Efficient Solar-Light Active Magnetic Photocatalyst for the Degradation of Pharmaceutical Active Compounds.

For applications related to the photocatalytic degradation of environmental contaminants, engineered nanomaterials (ENMs) must demonstrate not only a high photocatalytic potential, but also a low tendency to agglomeration, along with the ability to be easily collected after use. In this manuscript, a two-step process was implemented for the synthesis of ZnO, ZnO/Bentonite and the magnetic ZnO/γ-Fe2O3/Bentonite nanocomposite. The synthesized materials were characterized using various techniques, and their performance in the degradation of pharmaceutical active compounds (PhACs), including ciprofloxacin (CIP), sulfamethoxazole (SMX), and carbamazepine (CBZ) was evaluated under various operating conditions, namely the type and dosage of the applied materials, pH, concentration of pollutants, and their appearance form in the medium (i.e., as a single pollutant or as a mixture of PhACs). Among the materials studied, ZnO/Bentonite presented the best performance and resulted in the removal of ~95% of CIP (5 mg/L) in 30 min, at room temperature, near-neutral pH (6.5), ZnO/Bentonite dosage of 0.5 g/L, and under solar light irradiation. The composite also showed a high degree of efficiency for the simultaneous removal of CIP (~98%, 5 mg/L) and SMX (~97%, 5 mg/L) within 30 min, while a low degradation of ~5% was observed for CBZ (5 mg/L) in a mixture of the three PhACs. Furthermore, mechanistic studies using different types of scavengers revealed the formation of active oxidative species responsible for the degradation of CIP in the photocatalytic system studied with the contribution of h+ (67%), OH (18%), and ·O2- (10%), and in which holes (h+) were found to be the dominant oxidative species.

Kinetics and mechanisms of the carbamazepine degradation in aqueous media using novel iodate-assisted photochemical and photocatalytic systems.

The present study investigates the kinetics and mechanisms of carbamazepine (CBZ) degradation using a novel UV/iodate (IO3-) system for the first time and explores the influence of process conditions on its degradation. UV/IO3- showed high degradation efficiencies in a wide range of pHs, especially under neutral and acidic conditions, indicating that the system can be considered as a promising method to deal with effluents under various pH conditions. Radical scavenging experiments show that both iodine radicals (IO, IO2 and IO3) and hydroxyl radicals play an important role in CBZ degradation. Furthermore, the combination of UV/IO3- with TiO2 was studied to explore the potential of the addition of IO3- to improve the efficiency of the conventional TiO2 photocatalytic system. Scavenging experiments indicated that iodine radicals (IO, IO2 and IO3) were mainly involved in the degradation of CBZ in the UV/IO3-/TiO2 system, and the reaction mechanism equations were proposed for the first time for the studied UV/IO3-/TiO2 system. Several degradation products and four possible pathways of CBZ degradation were also elucidated using ultra-high-performance liquid chromatography in combination with a quadrupole time-of-flight mass spectrometer (Q-TOF MS). Respirometric tests indicated that the treatment has a positive impact on biomass behavior during subsequent biological purification, highlighting that the developed IO3--assisted AOPs are eco-friendly.

Low temperature Moving Bed Bioreactor denitrification as mitigation measure to reduce agricultural nitrate losses.

The negative impact of agriculture on the quality of local water streams is widely recognized. Fertilizer residues not taken up by the crops leach into the drainage water and enter the surface water, resulting in eutrophication. Despite various initiatives to prevent this leaching by optimizing fertilizer schemes, the desired effect was not achieved, and the focus has shifted to denitrifying end-of-pipe techniques. Because the available area for installing such treatment systems is often limited, the development of intensified systems is a trend that has emerged recently. In this scope, the main goal of this study was therefore to investigate the suitability of a denitrifying Moving Bed Bioreactor (MBBR) as a low footprint technology, which can compete with conventional technologies. Two parallel lab-scale pilot MBBRs, one at low temperature and one at ambient temperature, were operated for 850 days to investigate the effectiveness and robustness under changing process parameters (hydraulic retention time (HRT), temperature, shutdown). Eventually, the system was scaled up to a full-scale installation and monitored during a full drainage season in the field. The pilot-scale MBBRs achieved removal efficiencies above 90% under optimal conditions (high C/N ratio and minimal HRT of 8 h), even while operating at low temperatures. The robustness of the system was also demonstrated by the immediate start-up after a shutdown period of 220 days. Overall, the full-scale MBBR treated 2910.1 m3 drainage water and removed approximately 59 kg NO3-N. Unfortunately, the average removal efficiency, i.e., 70%, was lower than the lab-scale system, but by intensifying the mixing in the MBBR, improved results were obtained. Nitrite accumulation was furthermore also prevented.

Role of carrier characteristics affecting microbial density and population in enhanced nitrogen and phosphorus removal from wastewater.

This research aims to improve simultaneous nitrification-denitrification and phosphorus removal (SNDPR) using novel carriers and to demonstrate the effect of carrier characteristics on nutrient removal in a biofilm reactor. For this purpose, biofilms enriched with both polyphosphate-accumulating organisms (PAOs) and nitrifiers were cultivated in two parallel sequencing batch reactors containing conventional moving bed bioreactor carriers (MBBR) and a novel type of carriers (carbon-based moving carriers (CBMC)). The new carriers were produced based on recycled waste materials via a chemical-thermal process and their specific surface area were 10.4 times higher than typical MBBR carriers of similar dimensions. The results showed that the use of CBMC carriers increased bacterial adhesion by about 18.5% and also affected the microbial population inside the biofilms, leading to an increase in PAOs abundancy and thus an increase in biological phosphorus removal up to 12.5%. Additionally, it was corroborated that the volume of the anoxic zones with dynamic behavior is strictly influenced by the carrier structure and biofilm thickness due to a limitation in oxygen penetration. Accordingly, the formation of broader anoxic zones and shrinkage of these zones to a lesser extent resulted in the continuation of anoxic reactions for longer periods using the novel carriers. Thereby, an increase in nitrogen removal by about 15% was obtained mainly by denitrifying PAOs. The results also exhibited that a higher simultaneous nitrification-denitrification (SND) efficiency can be achieved by selecting an appropriate aeration program influencing the dynamic changes of anoxic zones. Overall, a biofilm system using the new carriers, with phosphorus and nitrogen removal efficiencies of 97.5% and 92.3%, was presented as an efficient, compact, and simple operation SNDPR process.

Indicators for resource recovery monitoring within the circular economy model implementation in the wastewater sector.

The European Union is currently in the process of transformation toward a circular economy model in which different areas of activity should be integrated for more efficient management of raw materials and waste. The wastewater sector has a great potential in this regard and therefore is an important element of the transformation process to the circular economy model. The targets of the circular economy policy framework such as resource recovery are tightly connected with the wastewater treatment processes and sewage sludge management. With this in view, the present study aims to review existing indicators on resource recovery that can enable efficient monitoring of the sustainable and circular solutions implemented in the wastewater sector. Within the reviewed indicators, most of them were focused on technological aspects of resource recovery processes such as nutrient removal efficiency, sewage sludge processing methods and environmental aspects as the pollutant share in the sewage sludge or its ashes. Moreover, other wide-scope indicators such as the wastewater service coverage or the production of bio-based fertilizers and hydrochar within the wastewater sector were analyzed. The results were used for the development of recommendations for improving the resources recovery monitoring framework in the wastewater sector and a proposal of a circularity indicator for a wastewater treatment plant highlighting new challenges for further researches and wastewater professionals.

Efficiency and mechanism of 2,4-dichlorophenol degradation by the UV/IO4- process.

This study explores the efficiency and kinetics of the photoactivated periodate process for the degradation of 2,4-dichlorophenol (2,4-DCP) in water. The obtained results show that the degradation rate was considerably higher for UV/IO4- compared to UV irradiation alone. Pseudo first-order reaction rate kinetics were obtained for all process conditions. The pH did not have a significant impact on the decomposition of 2,4-DCP using photoactivated periodate. Therefore, the applied method can be used to treat (waste)water at various pH. By raising the initial concentration of periodate to 5 mM, the degradation rate increased, while it decreased again at a concentration of 8 mM. As the 2,4-DCP concentration increased, the removal rate decreased. The extent of degradation was observed to be proportional with the UV intensity. A mechanistic study revealed that iodine radicals dominated the degradation of 2,4-DCP by photoactivated periodate, whereas OH and O(3P) only played a minor role. At pH 5.0, all chlorine atoms in 2,4-DCP were released as chloride ions in the UV/IO4- process, hence reaching a total dechlorination. Finally, the presence of inorganic salts, even at high levels, did not significantly impact the degradation. According to the results achieved in this study, the UV/IO4- system can be considered as a valuable alternative to treat effluents containing chlorinated organic compounds such as pulp and paper mill effluents and brine (waste)water.