Organic Chlorine Research Articles

Analysis of environmental factors affecting the incidence of testicular cancer, with particular emphasis on testicular germ cell tumors (TGCTs). Literature review

Introduction: Testicular cancer is the most common malignancy among men in the 20-44 age group. Most of the incidence is testicular germ cell tumor. In recent years there has been a steady increase in the incidence of this cancer. For this reason, we analyzed available articles on environmental risk factors that may influence the incidence of increased testicular malignancies Material and methods: Review of the specialized literature in the field of urology and articles available on PubMed, searching by the keywords “testicular cancer,” “testicular cancer risk factors,” “germ cell tumor,” “tgct‘’Aim of the study: The purpose of the study is to review the available literature and research papers regarding risk factors for malignant tumors of the testis. Summary: In recent years, there has been an increase in the incidence of testicular cancer, especially among men aged 20-44 years. The vast majority of it is germ cell tumors (TGCT). This article discusses the influence of environmental factors on the development of testicular cancer, with particular emphasis on the induction of TGCT. Studies indicate an association between exposure to trichloroethylene and other solvents and the risk of TGCT induction. The role of exposure to pesticides (especially fungicides), organic chlorine compounds, and viruses was also indicated to increase the risk of developing TGCTs,. The association of neoplasia with marijuana and tobacco use has also been studied, but needs further research. There is a need for continued research regarding heavy metals, infertility and factors related to pregnancy and the perinatal period. It is necessary to know the mechanisms that induce the process of carcinogenesis in the testis, which will enable the use of prevention and prophylaxis.

Co-selective effect of dissolved organic matter and chlorine on the bacterial community and their antibiotic resistance in biofilm of drinking water distribution pipes

The proliferation of pathogenic bacteria and antibiotic resistance genes (ARGs) in the biofilm of drinking water distribution pipes poses a serious threat to human health. This work adopted 15 polyethylene (PE) pipes to study the co-selective effect of dissolved organic matter (DOM) and chlorine on the bacterial community and their antibiotic resistance in biofilm. The results indicated that ozone and granular activated carbon (O3-GAC) filtration effectively removed lignins and proteins from DOM, and chlorine disinfection eliminated carbohydrate and unsaturated hydrocarbons, which both contributed to the inhibition of bacterial growth and biofilm formation. After O3-GAC and disinfection treatment, Porphyrobacter, unclassified_d_bacteria, and Sphingopyxis dominated in the biofilm bacterial community. Correspondingly, the bacterial metabolism pathways, including the phosphotransferase system, phenylalanine, tyrosine and tryptophan biosynthesis, ABC transporters, and starch and sucrose metabolism, were downregulated significantly (p < 0.05), compared to the sand filtration treatment. Under such a situation, extracellular polymeric substances (EPS) secretion was inhibited in biofilm after O3-GAC and disinfection treatment, postponing the interaction between EPS protein and pipe surface, preventing bacteria, especially pathogens, from adhering to the pipe surface to form biofilm, and restraining the spread of ARGs. This study revealed the effects of various water filtration and disinfection processes on bacterial growth, metabolism, and biofilm formation on a molecular level, and validated that the O3-GAC filtration followed by chlorine disinfection is an effective and promising pathway to control the microbial risk of drinking water.

Assessment of an Advanced Water Filtration System for Enhanced Water Purification

The study confirms the effectiveness of a state-of-the-art water filtration system in purifying urban tap water, river water, and groundwater. The system, which uses activated carbon, ceramic, and reverse osmosis (RO) filtration, significantly improved water quality by removing physical, chemical, and biological contaminants. Key results include: The system achieves a turbidity reduction of up to 99.5%, adhering to WHO standards. The system removes over 96% of volatile organic compounds (VOCs) and chlorine, and more than 99% of heavy metals like lead and arsenic. The water is completely free of harmful bacteria, guaranteeing its microbiologic safety. There has been a 98.2% reduction in total dissolved solids (TDS) in groundwater. The study highlights the system's adaptability to diverse environments, including urban, rural, and industrial settings. Future research could focus on improving the system's energy efficiency and sustainability.

Chlorine evolution and char characteristics during pyrolysis upgrading of Xinjiang high chlorine coal

Xinjiang ShaErHu (SEH) coal, characterized by a high chlorine concentration exceeding 1 %, can cause severe chlorine corrosion when directly burned. To utilize this high-chlorine coal in an effective and clean way, specific pretreatments such as low-temperature pyrolysis upgrading are required. In this paper, the changes in tar, pyrolysis gas, combustion characteristics, and chlorine evolution features were analyzed during the low-temperature pyrolysis of SEH coal. The effects of increasing temperature (350 °C, 450 °C, and 550 °C) were studied. The results show that the proportion of aromatic compounds released consistently increases with temperature, reaching a peak of 80 % at 550 °C in the tar. It is noteworthy that chlorine is hardly detected in tar. The percentage of chlorine released in the pyrolysis gas remains relatively stable as the temperature rises from 350 °C to 550 °C, accounting for approximately 17.5 % of the total chlorine. The percentages of water-soluble chlorine in raw coal, char-350 °C, char-450 °C and char-550 °C are 74.3 %, 80.4 %, 82.2 %, and 55.1 % respectively. The majority of the chlorine in the char produced at 350 °C and 450 °C is inorganic, making up 68.9 % and 69.4 %, respectively. In contrast, char generated at 550 °C has 58.4 % chlorine that is primarily organic. About 40 % of the inorganic chlorine is converted to organic chlorine when the pyrolysis temperature is raised to 550 °C. This conversion likely occurs as a result of the inorganic chlorine ions combining with carbon to form C-Cl bonds. In order to effectively prevent high temperature corrosion, high-chlorine coal can be treated by pyrolysis at temperatures between 350 and 450 °C, followed by water washing and burning. This research provides a theoretical foundation for the clean and efficient use of high-chlorine coal.

Solar-driven chloride activation via 3D oxygen-vacancy-rich TiO2 network photoanode for ultrafast and durable purification of saline wastewater

Photoelectrochemical chloride activation (PEC-Cl) is a promising and reagent-free strategy to treat saline organic wastewater by activation of chloride (Cl–) using sunlight. However, the low efficiency and Cl– corrosion of photoelectrode, and the limited mass transfer of pollutant hinder its application. Herein we successfully solve these challenges by developing porous oxygen-vacancy-rich TiO2 nanoneedle arrays (TiO2 NNs-r400) photoanode. Under illumination, the photoinduced holes in TiO2 NNs-r400 oxidize Cl– to reactive species (e.g., HOCl, Cl•, Cl2•− and ClO•), resulting in the degradation rate of tetracycline hydrochloride (HTC, 0.861 min−1) by TiO2 NNs-r400/PEC-Cl system is 2–3 orders of magnitude higher than the state-of-the-art. Experiments and computational analysis indicate that oxygen vacancies (Ovs) on TiO2 NNs-r400 promote the photocarriers separation efficiency and more importantly, facilitate Cl– adsorption with intermediary strength and reduce the energy barriers of Cl– oxidation. Furthermore, we design a continuous flow-through PEC reactor for TiO2 NNs-r400/PEC-Cl technology. The process exhibits 100% HTC degradation (TOC = 60.23%) for over 2000 h flow-through operation, which maintains high activity in the treatment marine aquaculture wastewater with nearly zero energy consumption by directly utilize natural sunlight. In the final effluent, the toxicity of almost all degradation intermediates is decreased, and the formation of total organic chlorine is low (17.2 µg L–1). This work provides insights into Cl– activation on Ov-rich photoanode and strategy for practical application of solar energy in efficient, sustainable and eco-friendly wastewater decontamination.

The joint impact of PM2.5 constituents on the risk of cerebrovascular diseases hospitalization: A large community-based cohort study

Air pollution poses significant health risks to urban areas, with limited focus on the chronic association of PM2.5 and its constituents on cerebrovascular diseases (CERs), especially regarding the joint associations. This study explores the individual and joint associations between PM2.5 constituents and CER hospitalization risks through a cohort analysis of 36,271 adults in the Pearl River Delta, South China, from 2015 to 2020. Cox proportional hazards regression and quantile-based g-computation models were used to quantify the individual and joint associations of annual mean concentrations of PM2.5 constituents with hospitalization for CERs. 1151 participants were hospitalized due to CERs during the five-year follow-up period. Joint associations analyses identified that one quartile increase in co-exposure may result in hazard ratios of 1.530 (1.441–1.623), 1.840 (1.710–1.980), and 1.609 (1.491–1.737) for CERs, total, and ischemic stroke hospitalization, respectively. The adverse effect was primarily driven by organic matter and chlorine. Men, those with a history of tobacco or alcohol use or with low residential greenness, were more susceptible to CERs hospitalization following PM2.5 constituents co-exposure. Upcoming strategies should focus on monitoring and regulating PM2.5 constituents, encouraging healthy lifestyles, and enhancing urban greenery.

Electrochemical chlorine evolution reaction to improve the desalination of sea sand

Sea sand, a vital sand and gravel resource, is rich in chloride, which causes corrosion of steel reinforcements. This study investigates the effect of the electrochemical chlorine evolution reaction (CER) on the desalination of sea sand. The results indicate that the chlorine removal efficiency (RE) of sea sand increased from 48.76 to 56.40 % under optimal conditions: a current density of 15 mA/cm2, an electrolysis time of 1 min, and a sodium sulphate-supported electrolyte concentration of 0.05 mol/L. After 30 days of resting, the dissolved chlorine content in sea sand was 0.154 %, which was 21.03 % lower than that of the control group. The electrically active chlorine-mediated desalination process demonstrated excellent dechlorination ability, facilitated the transformation of metal and organic chlorine into liquid and gaseous forms, and reduced the slow release of chloride from sea sand. Therefore, CER is expected to be an efficient method for sea sand desalination.

Comparison of chlorine and chlorine dioxide disinfection in drinking water: Evaluation of disinfection byproduct formation under equal disinfection efficiency

Disinfection efficiency and disinfection byproduct (DBP) formation are two important aspects deserving careful consideration when evaluating different disinfection protocols. However, most of the previous studies on the selection of disinfection methods by comparing DBP formation were carried out under the same initial/residual dose and contact time of different disinfectants, and such a practice may cause overdose or underdose of a certain disinfectant, leading to the inaccurate evaluation of disinfection. In this study, a comprehensive and quantitative comparison of chlorine (Cl2) and chlorine dioxide (ClO2) disinfection was conducted with regard to their DBP formation under equal disinfection efficiency. The microbial inactivation models as well as the Cl2 and ClO2 demand models were developed. On such basis, the integral CT (ICT) values were determined and used as a bridge to connect disinfection efficiency and DBP formation. For 3-log10 and 4-log10 reductions of Pseudomonas aeruginosa, ClO2 had 1.5 and 5.8 times higher inactivation ability than Cl2, respectively. In the premise of equal disinfection efficiency (i.e., the ICT ratios of Cl2 to ClO2 = 1.5 and 5.8), the levels of total organic chlorine, total organic bromine, and total organic halogen formed in the Cl2 disinfection were significantly higher than those formed in the ClO2 disinfection. Among the 35 target aliphatic DBPs, trihalomethanes (THMs) and haloacetic acids (HAAs) were the dominant species formed in both Cl2 and ClO2 disinfection. The total THM levels formed in Cl2 disinfection were 14.6 and 30.3 times higher than those in ClO2 disinfection, respectively. The total HAA levels formed in Cl2 disinfection were 3.5 and 5.4 times higher than those in ClO2 disinfection, respectively. Formation of the target 48 aromatic DBPs was much favored in Cl2 disinfection than that in ClO2 disinfection, and the formation levels was dominated by contact time. This study demonstrated that ClO2 had significant advantages over Cl2, especially at higher microorganism inactivation and lower DBP formation requirements.

Overlooked competition and promotion effects in electrochemical oxidation of humic acid and ammonia in landfill leachate

Electrochemical oxidation (EO) can effectively reduce the degree of humification and toxicity of landfill leachate by generating highly active oxidative species in situ. However, the selective and competitive oxidation of humic acid (HA) and ammonia (NH4+) and the role of different oxidative species during the EO process in complex aqueous conditions remain unclear. In this study, a nanostructured tin-antimony electrode (Ti/Sb-SnO2 NFs) was prepared and compared with three types of commercial electrodes (Ti/Ir-RuO2, Ti4O7, Ti/Sb-SnO2) in terms of electrochemical properties and electrocatalytic oxidation of HA and NH4+. The de-humification capacity, interactive effects of HA and NH4+ on each other's oxidation by different oxidative species, as well as the related oxidation byproducts were investigated. The differences in pollutant electrooxidation among the different electrodes were found to be insignificant. The presence of HA was found to be detrimental to NH4+ degradation while reducing the N2 conversion rate. Interestingly, NH4+ initially inhibited the degradation rates of HA while promoted the degradation and reduced the accumulation of organic chlorine during the later EO process. A proposed mechanism accounts for both competitive and promotional effects for simultaneous HA and NH4+ oxidation during the EO process.

Study of the migration and distribution pathways of key corrosive species during high-temperature corrosion by means of atom probe tomography and δ35Cl isotope tracer

This study investigated the migration pathways and the dominant chlorine- and alkali-induced corrosion mechanisms of Ni-28Cr-13Al-0.6B-0.5 W alloy at 600ºC. The distribution of key elements (35Cl, 37Cl, Na, O, Ni, Cr, Al) at the alloy/oxide interface was analyzed by APT coupled with δ35Cl isotope labeling for tracing the competitiveness of organic chlorine and inorganic chlorine. The alloying element`s migration rate was in the order of Al > Cr > Ni > W. Cl diffused through oxide grain-boundaries as Cl- ions formed by the decomposition of sulfate-melt and corrosion in grain-boundaries was dominated by electrochemical reaction mechanisms. Na enhances the diffusion of elements by widening the grain-boundaries.

A validated reverse-phase LC-MS/MS method for the analysis of haloacetic acids in drinking water: supporting the transition from HAA5 to HAA9

ABSTRACT Haloacetic acids (HAAs) are potentially toxic by-products formed from interactions between organic matter and chlorine during disinfection of drinking water, with brominated HAAs forming when bromide is present. Some countries require monitoring of drinking water for five HAAs, but there is increasing health concern related to the more toxic brominated HAAs and monitoring of nine HAAs (HAA9) is becoming more widespread. However, existing methods of analysis for HAA9 are often sub-optimal, involving complex derivatisation steps and/or long analytical run times. This article presents an improved methodology utilising reverse-phase liquid chromatography mass spectrometry (LC-MS/MS) for which sample preparation involves simple pH adjustment and the analytical run takes 10 min. The efficacy of the method was demonstrated by a full validation across four drinking water matrices with good sensitivity (&amp;lt;0.8 μg/L), precision (&amp;lt;7%), and bias (&amp;lt;10%) observed. A direct comparison using real water samples was performed against the widely used existing gas chromatography method. The new LC-MS/MS method was significantly quicker and easier and demonstrated improved performance in terms of accuracy and precision. This has implications for understanding the risk posed by HAAs in chlorinated water by eliminating the possible historical under-estimates of the levels of the more toxic brominated compounds.

Efficiently removing dissolved organic pollutants in landfill leachate concentrate using dual-anode Fe2+/HClO system: The significance of insolubilization based on oxidative coupling of organics

The strategy to mineralize dissolved organics for the decontamination of landfill leachate concentrate (LLC) is expensive. Because mineralization requires high stoichiometric ratio of oxidants (e.g., •OH) or electron transfer (i.e., energy) to the pollutant molecules. Whereas, transferring the dissolved organic pollutants into separable insoluble matters is an energy-saving strategy. Herein, we developed a dual-anode Fe2+/HClO system for removing dissolved organic pollutants in LLC through insolubilization based on oxidative coupling. In this system, the majority of dissolved organic pollutants were transferred into insoluble substances, which could be removed easily. As a result, 89.8 % of the dissolved organic carbon (DOC) in LLC was fast removed in 3 h with a low specific energy consumption (SEC, 4.0 kWh kg−1 COD and 17.6 kWh kg−1 DOC), and the formation of toxic by-products can be well controlled to total organic chlorine (TOCl) < 0.1 mg/L. The formation of insoluble substances was attributed to the oxidative coupling of organic small molecules into the macromolecular ones. This was evidenced by the generation of insoluble compounds with the larger molecular mass, and the formation of coupling or polymerization products of the model pollutant (guaiacol). The predominant mechanism was proposed that Fe(IV) was generated in the dual-anode Fe2+/HClO system, and Fe(IV) oxidized pollutants to produce organic radicals, then the organic radicals coupled and polymerized to form larger molecules and insoluble compounds. This work offers a novel electrochemical method for efficient removal of organic pollutants in LLC with minimal toxic by-products generated, and revealed the significance of oxidative coupling process in the electrochemical Fe2+/HClO system.

East Asian summer monsoon delivers large abundances of very short-lived organic chlorine substances to the lower stratosphere

Deep convection in the Asian summer monsoon is a significant transport process for lifting pollutants from the planetary boundary layer to the tropopause level. This process enables efficient injection into the stratosphere of reactive species such as chlorinated very-short-lived substances (Cl-VSLSs) that deplete ozone. Past studies of convective transport associated with the Asian summer monsoon have focused mostly on the south Asian summer monsoon. Airborne observations reported in this work identify the East Asian summer monsoon convection as an effective transport pathway that carried record-breaking levels of ozone-depleting Cl-VSLSs (mean organic chlorine from these VSLSs ~500 ppt) to the base of the stratosphere. These unique observations show total organic chlorine from VSLSs in the lower stratosphere over the Asian monsoon tropopause to be more than twice that previously reported over the tropical tropopause. Considering the recently observed increase in Cl-VSLS emissions and the ongoing strengthening of the East Asian summer monsoon under global warming, our results highlight that a reevaluation of the contribution of Cl-VSLS injection via the Asian monsoon to the total stratospheric chlorine budget is warranted.

Fate of sulfur and chlorine during co-incineration of municipal solid waste and industrial organic solid waste

In China, the co-incineration of municipal solid waste (MSW) with industrial organic solid waste (IOSW) is increasingly adopted. Compared with MSW, IOSW contains higher levels of sulfur (S) and chlorine (Cl), presenting significant challenges for controlling S/Cl emissions in MSW incineration plants. In this study, the impact of co-incinerating IOSW was investigated in a 500 t/d incinerator grate, focusing on the emissions and transformation behaviors of S/Cl. IOSW, with a consistent sulfur content of about 0.22 wt% and a more variable chlorine content averaging 0.53 wt%, contains over 40 % organic sulfur and >90 % organic chlorine, higher than in MSW. The results of co-incineration experiments showed that the median SO2 concentration in the flue gas was stable at 50 mg/m3, while HCl concentration decreased initially and then increased as the co-incineration ratio of IOSW rose from 20 % to 40 %. Furthermore, the concentrations of SO2 and HCl were not significantly influenced by wind flow but were positively affected by the rising furnace temperatures. Besides, the co-incineration ratio had minimal impact on sulfur in fly ash before deacidification, primarily derived from the gas stream. However, the (Na + K)/Cl ratio in fly ash progressively increased from 1.5 to 1.9, and the Ca content decreased from 0.35 % to 0.15 % as the co-incineration ratio rose to 40 %, indicating more chlorine migration into the fly ash at higher co-incineration rates. This research offers essential guidance for effectively controlling pollutant emissions during the co-incineration of IOSW, specifically the S/Cl pollutants.

Sustainability of Electrocoagulation Process in the Removal of Dicofol Pesticide using Aluminium Electrodes

Because of its different concentrations, sewage can cause serious water pollution problems for aquatic organisms. Dicofol is a pesticide derived from organic chlorine that effectively targets ticks, though it is a subject of controversy because of its negative effects on the environment. In this study, an aluminium electrode was employed for the elimination of dicofol from a water-based solution through the process of electrocoagulation. Aluminium electrodes are characterized by SEM and FTIR techniques. The optimization process for several parameters such as the maximum removal percentage of Dicofol by APE was determined under the optimized conditions: electrolysis time, NaCl concentration, voltage, pH, initial Dicofol concentration. The pseudo-first-order rate constant of the aluminium plate electrodes was determined according to the results of the kinetic study. The electrical energy used to remove dicofol in the electrocoagulation process was determined on aluminium plate electrodes.

Evolution and speciation transformation of chlorine during automobile shredder residue pyrolysis

Disposal of automobile shredder residue (ASR) via pyrolysis enables the recovery of valuable products; however, the production of hazardous pollutants and low-value products is inevitable due to its high chlorine content. In this work, chlorine evolution behavior and the conversion mechanism during ASR pyrolysis between 480 and 600 °C were systematically studied. The experimental results for organic chlorine (Org-Cl) showed that released chlorinated gases were complex, and HCl only accounted for 35% of the gas phase products, while short-chain hydrocarbons with carbon atoms between two and four accounted for 52%. Chlorine was predominantly retained in the char, and Org-Cl was the primary contributor to the residual chlorine, accounting for over 50% of the char. The content of inorganic chlorine (InO-Cl) was low in the raw sample but significantly increased in the char. Through the distinction between organic and inorganic chlorine content in char, it was confirmed that Org-Cl could be converted to InO-Cl due to complex secondary reactions with metallic compounds. The conversion was favored by increasing the Org-Cl content and the temperature. Our findings clarified the evolution mechanism of chlorine and the transformation from Org-Cl to InO-Cl, thus providing guidance for chlorine regulation and the efficient recycling of metal resources.

The Migration of Organic Chlorine Pesticide Residues in the Composition of the Soil Samples from Mirzaabad, Gulistan and Boyovut Districts of Syrdarya Region

The thin layer chromatography gas chromatography ECD detector was employed to evaluate soil samples and wheat stalks collected during the spring season for the presence of chlorine organic pesticides, namely DDT, DDE, DDD, HCH alpha, and gamma isomers. The study revealed that the uppermost concentration of pesticides is constrained within the depth interval of 0–10(20) cm, with their infiltration extending to a depth of 2.0–2.5 m. The initial investigation focused on examining the dynamics and movement of OCP, including substances such as DDT, DDD, DDE, alpha HCH, and gamma HCH, throughout the Syrdarya region. This page provides an overview of organochlorine pesticides, their residual presence, their application in agricultural regions, and the constituent makeup of wheat stalks. In April 2023, a collection of samples was obtained from several districts within the Syrdarya region. Subsequently, a comprehensive analysis was conducted on a total of 15 samples. The gas chromatography technique with an electron capture detector (GC/ECD) was employed for the investigation of organic chlorine insecticides. The isolation and quantification of organic chlorine insecticides with low to medium polarity were achieved using a capillary column.

Comparison on the formation and toxicity for chlorinated products during the oxidation of acetic acid (CH3COOH) by three widely used advanced oxidation processes (AOPs) at the presence of [formula omitted]

As a technology for industrial wastewater advanced treatment, there is a lack of relevant information the impacts of the treated effluents by advanced oxidation processes (AOPs) on ecological environment. Therefore, this study mainly compared the differences of the formation types and concentrations of chlorinated organic products（COPs）and active inorganic chlorine species (AICS) and toxicity changes in the oxidation of CH3COOH by three commonly used AOPs technologies as Fenton, ozone and electrochemical advanced oxidation process (EAOP) with the addition of Cl−. The results illustrate that in the EAOP process, trichloromethane (TCM) and Chloroacetic acids (CAAs) were the main COPs in the oxidation of CH3COOH by EAOP at 120 min. CCl4 was major COPs for the Fenton and ozone oxidation of CH3COOH, respectively. Through the algae growth inhibition experiment and the toxicity evaluation by using ECOTOX toxicity database, the toxicity of EAOP oxidation of CH3COOH to algae and fish were much higher than those from Fenton and ozone oxidation as the highest formation concentrations of inorganic by-products. Considering the toxic effects on the environment, when choosing the AOPs for the further treatment of wastewater containing Cl−, try to avoid the use of EAOP technology, and it is better to choose Fenton and ozone oxidation.

Core taxa, co-occurrence pattern, diversity, and metabolic pathways contributing to robust anaerobic biodegradation of chlorophenol

It is hard to achieve robustness in anaerobic biodegradation of trichlorophenol (TCP). We hypothesized that specific combinations of environmental factors determine phylogenetic diversity and play important roles in the decomposition and stability of TCP-biodegrading bacteria. The anaerobic bioreactor was operated at 35 °C (H condition) or 30 °C (L condition) and mainly fed with TCP (from 28 μM to 180 μM) and organic material. Metagenome sequencing was combined with 16S rRNA gene amplicon sequencing for the microbial community analysis. The results exhibited that the property of robustness occurred in specific conditions. The corresponding co-occurrence and diversity patterns suggest high collectivization, degree and evenness for robust communities. Two types of core functional taxa were recognized: dechlorinators (unclassified Anaerolineae, Thermanaerothrix and Desulfovibrio) and ring-opening members (unclassified Proteobacteria, Methanosarcina, Methanoperedens, and Rubrobacter). The deterministic process of the expansion of niche of syntrophic bacteria at higher temperatures was confirmed. The reductive and hydrolytic dechlorination mechanisms jointly lead to C–Cl bond cleavage. H ultimately adapted to the stress of high TCP loading, with more abundant ring-opening enzyme (EC 3.1.1.45, ∼55%) and hydrolytic dechlorinase (EC 3.8.1.5, 26.5%) genes than L (∼47%, 10.5%). The functional structure (based on KEGG) in H was highly stable despite the high loading of TCP (up to 60 μM), but not in L. Furthermore, an unknown taxon with multiple functions (dechlorinating and ring-opening) was found based on genetic sequencing; its functional contribution of EC 3.8.1.5 in H (26.5%) was higher than that in L (10.5%), and it possessed a new metabolic pathway for biodegradation of halogenated aromatic compounds. This new finding is supplementary to the robust mechanisms underlying organic chlorine biodegradation, which can be used to support the engineering, regulation, and design of synthetic microbiomes.

Pd nanoparticles supported on microflower NiMOF modified roughed nickel foam with the enhanced active site for electrochemical dechlorination of trichloroacetic acid

Electrocatalytic hydrodechlorination (ECH) has been considered as an effective method to convert refractory chlorinated organics into biodegradable chlorine-free organics under mild conditions. In this work, a composite electrode of Pd/NiMOF/roughed nickel foam (Pd/NiMOF/RNF) with excellent dechlorination performance was prepared by electrodeposition of Pd nanoparticles on the flower-shaped NiMOF interlayer grown in-situ. Benefiting from the high specific surface area of NiMOF structure and excellent dispersion of Pd facilitated, the Pd/NiMOF/RNF offered abundant active hydrogen and larger open channels for the easy diffusion of reactants and products in the electrochemical dechlorination process. 97% of 6 μmol/L trichloroacetic acid (TCAA) was dechlorinated at a cathodic potential of −1.2 V within 90 min. The corresponding palladium mass activity was calculated to be 0.39 μg min−1 cm−2 mg−1 Pd, which was approximately 3.5 times greater than other report on ECH cathode. Moreover, the Pd/NiMOF/RNF cathode remained stable even after five consecutive cycle tests. Toxic assessment results indicated that the dechlorination process was beneficial to the detoxification of TCAA at the end of reaction. The hydrodechlorination mechanism of TCAA was proposed by density functional theory (DFT) analysis and electrochemical characterization on the Pd/NiMOF/RNF electrode. The findings of this study have the potential to contribute to the development of electrocatalytic treatment methods for chlorinated organic compounds in drinking water.