Organic Pollutants Research Articles

Developmental toxicity and potential mechanisms exposed to polystyrene microplastics and polybrominated diphenyl ethers during early life stages of fat greenling (Hexagrammos otakii)

The occurrence of microplastics (MPs) in aquatic ecosystems and their ability to absorb hydrophobic pollutants, such as persistent organic pollutants (POPs), is currently a significant concern. MPs, which are the main breakdown product of plastics, have been frequently detected in the environment, posing serious threats to organisms’ health. One particular pollutant, 2,2′,4,4′-tetrabromodiphenyl ether (BDE-47), is a dominant congener of PBDEs and is highly toxic to organisms. However, there is limited knowledge regarding the exposure of marine fishes to PBDEs through MPs and their combined toxic effects. In this study, the embryo toxicity of Hexagrammos otakii was conducted to investigate the combined effects of MPs and BDE-47. The results showed that MPs and BDE-47 co-exposure had detrimental effects on embryonic development, such as reduced hatchability, increased mortality, decreased heart rate, and body malformation. Moreover, the combined toxicity of these substances appeared more pronounced harmful effects compared to exposure to BDE-47 alone. Histopathological examination revealed that co-exposure can cause greater damage to hatching glands and yolk. The enrichment of Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways included phagosome, metabolism of xenobiotics by cytochrome P450, TCA cycle, and Wnt signaling pathway, which are closely related to embryonic growth. BDE-47 and MPs may activate the Wnt signaling pathway to affect the normal development of embryos. Our results suggest that MPs and BDE-47 exposure may cause growth disorders in the early life stages of H.otakii, leading to abnormal embryonic development. All these results will contribute to the further study of the ecological risk assessment and toxicity of MPs and organic pollutant mixtures in marine fish.

Magnetically separable Z-scheme ZnFe2O4/MoS2 photocatalyst for boosting photo-Fenton degradation activity by a hole-mediated mechanism

The development of high-efficiency and robust photocatalysts is imperative and challenging in advanced oxidation processes (AOPs). Herein, magnetically separable ZnFe2O4/MoS2 photocatalyst was prepared by a simple hydrothermal method. The degradation characteristics of several organic pollutants (rhodamine B (RhB), methyl orange, methylene blue, and antibiotic tetracycline) were investigated with/without the addition of H2O2 under visible light irradiation. It is found that the synergistic effect of Z-scheme ZnFe2O4/MoS2 photocatalyst and photo-fenton-like reaction promotes the decomposition of H2O2, accelerates the separation efficiency of photogenerated electrons and holes, and thus improves the photocatalytic activity. The RhB photo-degradation of the constructed Z-scheme ZnFe2O4/MoS2 (96.3%) photocatalyst in the absence of H2O2 for 100min is better than that of MoS2 (74.8%) and ZnFe2O4 (6.2%), with a rate constant of 0.0332min-1. The slight amount of H2O2 boosts the photocatalytic performance significantly. Its degradation rate is 98.6% within 8min with the rate constant of 0.396min-1, 12 times higher than that of ZnFe2O4/MoS2 photocatalyst without H2O2. The magnetic separation, recycling stability and neutral solution process are also confirmed in ZnFe2O4/MoS2 system, indicating the enormous potential of this photocatalyst in environmental remediation and waste water treatment. The hole-mediated oxidation mechanism has been proposed instead of conventional active radicals of •OH based on the free radicals capture and electron spin resonance experiments. MoS2 plays a crucial role in facilitating the H2O2 decomposition and realizing the conversion circulation from Fe3+ to Fe2+ by the redox cycling as a co-catalyst. This study provides insights into the photocatalytic mechanism of Z-scheme photo-Fenton heterojunction photocatalysts, conducive to the development of high-efficient and stable photocatalysts in AOPs.

Photocatalytic Performance of the BaSn-based Nanoscale Materials for the Organic Pollutants Enhanced by Sm (Er) Doping

Background: Sm (Er) doping is an effective strategy for enhancing the photocatalytic activity of the semiconductor photocatalysts for the degradation of organic pollutants. BaSnbased nanorods possess wide band gap energy, which limits the photocatalytic application. It is important to research the feasibility of the improved photocatalytic performance of the BaSnbased nanorods by doping with Sm (Er). Objective: The aim is to synthesize Sm (Er)-doped BaSn-based nanoscale materials through a simple hydrothermal process and research the photocatalytic performance of the Sm (Er)-doped BaSn-based nanoscale materials for the gentian violet degradation. Methods: Sm (Er)-doped BaSn-based nanoscale materials with a polycrystalline structure were synthesized through a simple hydrothermal process. The Sm (Er)-doped composites were analyzed by X-ray diffraction, electron microscopy, solid diffuse reflectance spectrum, X-ray photoelectron spectroscopy, photoluminescence, and electrochemical impedance spectroscopy. Results: Sm (Er) doping induces the morphological evolution of the BaSn-based nanoscale materials from the nanorods to irregular nanoscale particles. Sm (Er) in the doped BaSn-based nanoscale materials exists in the form of the cubic Sm2Sn2O7 and orthorhombic ErF3 phases. The band gap value is decreased with increasing the Sm (Er) dopant contents. Sm (Er)-doped BnSnbased nanoscale materials with the Sm (Er) content of 8wt.% have the lowest band gap and show the strongest light absorption ability. Compared with the un-doped BaSn-based nanoscale materials, the Sm (Er)-doped BnSn-based nanoscale materials exhibit higher photocatalytic activity for the gentian violet degradation. 8wt.% Sm-doped BnSn-based nanoscale materials show the highest photocatalytic activity for the degradation of the gentian violet. 20 mL gentian violet solution (concentration of 10 mg·L-1) can be totally degraded using 20 mg 8wt.% Sm-doped BnSnbased nanoscale materials under UV light illumination for 150 min. Conclusion: The enhanced photocatalytic activity of the Sm (Er)-doped BnSn-based nanoscale materials can be attributed to the decreased band gap, enhanced light absorption ability, and decreased recombination of the photo-generated electron-hole pairs.

Chemical contamination affecting filter-feeding bivalves in no-take marine protected areas from Brazil

Marine protected areas (MPAs) are zones geographically delimited under pre-defined management goals, seeking to reduce anthropogenic threats to biodiversity. Despite this, in recent years reports of MPAs affected by chemical contamination has grown. Therefore, this study addresses this critical issue assessing legacy and current chemical contamination in filter-feeder bivalves obtained in very restrictive no-take MPAs from Brazil. The detected pollutants encompass polycyclic aromatic hydrocarbons (PAHs), linear alkylbenzenes (LABs), and persistent organic pollutants (POPs) like dichlorodiphenyltrichloroethane (DDTs) and polychlorinated biphenyls (PCBs). Despite protective measures, bivalves from nine MPAs exhibited high LABs (13.2–1139.0 ng g−1) and DDTs levels (0.1–62.3 ng g−1). PAHs were present in low concentrations (3.1–29.03 ng g−1), as PCBs (0.7–6.4 ng g−1), hexachlorobenzene (0.1–0.2 ng g−1), and Mirex (0.1–0.3 ng g−1). Regardless of the sentinel species, MPAs and management categories, similar accumulation patterns were observed for LABs, DDTs, PAHs, and PCBs. Based on the limits proposed by Oslo Paris Commission, the measured levels of PAHs, PCBs and were below the environmental assessment criteria. Such findings indicate the no biological effects are expected to occur. However, they are higher considering background conditions typically measured in remote or pristine areas and potential simultaneous exposure. Such findings indicate an influence of anthropogenic sources, emphasizing the urgency for monitoring programs guiding strategic management efforts to safeguard these areas.

Nanoplastics aggravated TDCIPP-induced transgenerational developmental neurotoxicity in zebrafish depending on the involvement of the dopamine signaling pathway

Plastics pose a hazard to the environment. Although plastics have toxicity, microplastics (MPs) and nanoplastics (NPs) are capable of interacting with the rest pollutants in the environment, so they serve as the carriers and interact with organic pollutants to modulate their toxicity, thus resulting in unpredictable ecological risks. PS-NPs and TDCIPP were used expose from 2h post-fertilization (hpf) to 150 days post-fertilization (dpf) to determine the bioaccumulation of tris(1,3-dichloro-2-propyl) phosphate (TDCIPP) and its potential effects on neurodevelopment in F1 zebrafish (Danio rerio) offspring under the action of polystyrene nano plastics (PS-NPs). The exposure groups were assigned to TDCIPP (0, 0.4, 2 or 10µg/L) alone group and the PS-NPs (100µg/L) and TDCIPP co-exposed group. F1 embryos were collected and grown in clean water to 5 dpf post-fertilization. PS-NPs facilitated the bioaccumulation of TDCIPP in the gut, gill, head，gonad and liver of zebrafish in a sex-dependent manner and promoted the transfer of TDCIPP to their offspring, thus contributing to PS-NPs aggravated the inhibition of offspring development and neurobehavior of TDCIPP-induced. In comparison with TDCIPP exposure alone, the combination could notably down-regulate the levels of the dopamine neurotransmitter, whereas the levels of serotonin or acetylcholine were not notably different. This result was achieved probably because PS-NPs interfered with the TDCIPP neurotoxic response of zebrafish F1 offspring not through the serotonin or acetylcholine neurotransmitter pathway. The increased transfer of TDCIPP to the offspring under the action of PS-NPs increased TDCIPP-induced transgenerational developmental neurotoxicity, which was proven by a further up-regulation/down-regulation the key gene and protein expression related to dopamine synthesis, transport, and metabolism in F1 larvae, in contrast to TDCIPP exposure alone. The above findings suggested that dopaminergic signaling involvement could be conducive to the transgenerational neurodevelopmental toxicity of F1 larval upon parental early co-exposure to PS-NPs and TDCIPP.

Blood and Tissue Levels of Persistent Organic Pollutants and Genetic Susceptibility in Patients with Breast Cancer

We investigated possible associations between the internal concentrations of POPs and correlations between blood and tumor tissue concentrations in patients who underwent surgery for breast cancer and breast reduction as controls. Genetic variations in CYP1A1, GSTP1, GSTM1, and GSTT1 and hOGG1 were evaluated to determine whether they represent risk factors for breast cancer. Certain POPs have been found to be associated with breast cancer development. GST-P1 polymorphism represented a significant risk for breast cancer with unadjusted OR. However, the GSTT1 null polymorphism represented a significant risk for breast cancer when OR adjusted for age and smoking status. CYP1A1 polymorphism was a significant risk factor for breast cancer, regardless of whether the OR was adjusted. These results suggest that exposure to certain POPs, GSTT1 and CYP1A1 polymorphisms, age, and smoking status are risk factors for breast cancer. In addition, the blood concentrations of some POPs represent surrogates for breast tissue concentrations.

Plasmon AgNPs/MoS2/ZnO nanorods array ternary heterojunctions enabling high-efficiency solar-light energy utilization for photocatalysis and recyclable SERS detection

BackgroundSurface-enhanced Raman scattering (SERS) has gained widespread use in molecule-level detection benefiting from its high sensitivity, nondestructive data acquisition, and capacity for providing molecular fingerprint information. However, the strong adhesion of target molecules to the substrate (known as the "memory effect") inherently hinders the reusability of SERS substrates. Research has shown that self-cleaning SERS substrates based on versatile semiconductor materials with SERS enhancement capabilities and solar photocatalytic properties offer an effective platform for the sensitive detection and degradation of harmful molecules. ResultsIn this research, a resuable SERS-active substrate was facilely fabricated by anchoring silver nanoparticles (AgNPs) to the edges of MoS2 nanosheet decorated on ZnO nanorod arrays (NRAs). This innovative design exhibited a remarkable SERS enhancement factor (EF) of 4.6 × 107 and demonstrated significant solar photocatalytic efficiency. Such superior characteristics of ternary plasma heterojunction were ascribable to the synergistic effect of the “Schottky barrier” and “hot spots” between MoS2 and AgNPs, the inherent chemical enhancement proficiency of the MoS2/ZnO NRAs heterojunction, as well as the ultrafast electron transfer within the ternary heterojunction. SignificanceThe developed ternary heterojunction substrate enabled highly sensitive SERS detection of trace amounts of organic molecules. Moreover, this SERS substrate exhibited self-cleaning and recyclability via solar-light-driven photocatalysis. This bifunctional recyclable SERS substrate proved capable of meeting various requirements for routine monitoring of environmental organic pollutants and provided a robust avenue for advancing energy utilization materials that serve as high-performance SERS sensors and catalysts.

Đánh giá mức độ phát thải của các chất polyclodibenzo-p-dioxin và polyclodibenzofuran phát sinh không chủ định từ lò đốt rác chất thải sinh hoạt và rác thải công nghiệp ở Việt Nam

Polychlorinated dibenzo-p-dioxins (PCDD) and polychlorinated dibenzofurans (PCDF) are the most toxic substances among the group of unintentional persistent organic pollutants (U - POP) generated from many sources, in which domestic and industrial waste incinerators are the highest emission risk. Assessment of pollution potential and dioxin/furan emissions from incinerators in developing countries, including Vietnam, is still limited; especially in-depth studies on the content and characteristics of PCDD/PCDF emitted into the atmosphere. Therefore, the research team evaluated the emission potential and characteristics of 07 PCDD and 10 PCDF, those are considered to be the most toxic isomers and congeners, from stack gas samples collected from incinerators at 33 facilities in 11 provinces in Vietnam. The total concentration of PCDD/PCDF in the industrial incinerators’ emission ranged from 37.3 to 3348.6 pg TEQs/m3 and domestic waste incinerators had lower total concentrations and fluctuated within about 37.3-1323.8 pg TEQs/m3. The characteristic of incinerator emissions is that the proportion of 2,3,7,8- TCDD accounts for 2.9 to 9.04%. The highest contributing concentrations were congeners 1,2,3,7,8-PeCDD, with its contributing percentage from 22.95-32.42%. The second largest contributor is congeners 2,3,4,7,8- PeCDF, accounting for 20.94- 21.50% of the total toxic congeners of PCDD/PCDF in both types of incinerators. However, in terms of toxic equivalency (TEQ), the concentration of industrial waste incinerators is much higher than that of domestic waste incinerators. The results of stack gas samples showed that the PCDD/PCDF content for domestic waste incinerators has 5/17 establishments that exceeded the permissible standard threshold: 0.6 ng/Nm3, according to QCVN 61-MT:2016/BTNMT. Industrial waste incinerators have 5/16 establishments that exceeded the permissible standard threshold: 0.6ng/Nm3 for furnaces with a capacity of 300kg/hour according to QCVN 30:2012/BTNMT.

Remediation of arsenic and fluoride from groundwater: a critical review on bioadsorption, mechanism, future application, and challenges for water purification.

In the past few decades, the excessive and inadequate use of technological advances has led to groundwater contamination, mainly caused by organic and inorganic pollutants, which are highly harmful to human health, agriculture, water bodies, and aquaculture. Among all toxic pollutants, As and F- play a significant role in groundwater contamination due to their excellent reactivity with other elements. To mitigate the prevalence of arsenic and fluoride within the water system, the use of biochar gives an attractive strategy for removing them mainly because of the substantial surface area, pore size, pH, aromatic structure, and functional groups inherent in biochar, which are primarily dependent upon its raw material and pyrolysis temperature. Researcher develops different methods like physiochemical and electrochemical for treating arsenic and fluoride contamination. Among all removal methods, bioadsorption using agricultural waste residues shows effective/feasible removal of As and F- due to its low cost, ecofriendly nature, readily available, and efficient reuse compared with several other harmful synthetic materials that demand costly design specifications. This study discusses current developments in bioadsorption methods for As and F- that use agricultural-based biomaterials and describes the prevailing state of arsenic and fluoride removal strategies that use biomaterials precisely.

Simultaneous Removal of Setazol Navy Blue and Cr(VI) By Mixed Microbial Culture Isolated from the Çubuk Stream

Water samples taken from the Çubuk Stream (Ankara, Turkey) were inoculated into nutrient broth media containing Setazol Navy Blue SBG (SNB), an organic pollutant, and heavy metal Cr(VI), an inorganic pollutant, to obtain a pollutant-resistant mixed microbial culture. Experiments were conducted with this culture to remove SNB and heavy metal. The optimum conditions, where the mixed bacterial culture removed the pollutants most effectively, were determined, showing that the highest capacity for removal took place at pH 8 with removal percentages 96.3% for Cr(VI) and 78.5% for SNB. In media with 50.4 mg/L SNB and 9.7 mg/L Cr(VI), the SNB removal was 87.3%, and the Cr(VI) removal was 96.6% at the end of the 7-day incubation period. The highest removal was observed with a biomass concentration of 8% (v/v) of mixed culture [50 mg/L SNB dye+25 mg/L Cr(VI)]. The removal was 100% for both Cr(VI) and the SNB dye. The bacteria with the highest removal were isolated and identified using 16S rDNA gene sequence analysis as Microbacterium oxydans and Leucobacter aridicollis. The role of various functional groups and the structures of the microorganisms that might be involved in the removal mechanisms were discussed using their FTIR spectra. This report is the first study that investigates a mixed bacterial culture and pure cultures (M. oxydans and L. aridicollis) isolated from that mixed culture, removing both SNB and Cr(VI) simultaneously.

Ultrathin BiOCl-OV/CoAl-LDH S-scheme heterojunction for efficient photocatalytic peroxymonosulfate activation to boost Co (IV)=O generation

Sustainable and rapid production of high-valent cobalt-oxo (Co(IV)=O) species for efficiently removing organic pollutants is challenging in permoxymonosulfate (PMS) based advanced-oxidation-processes (AOPs) due to the limitation of the high 3d-orbital electronic occupancy of Co and slow conversion from Co(III) to Co(II). Herein, S-scheme BiOCl-OV/CoAl-LDH heterojunction were constructed by ultrathin BiOCl with the oxygen-vacancy (OV) self-assembled with ultrathin CoAl-LDH. OV promoted the formation of charge transfer channel (Bi-O-Co bonds) at the interface of the heterojunction and reduced electron occupation of the Co 3d-orbital to facilitate the generation of Co(IV)=O in the BiOCl-OV/CoAl-LDH/PMS/Visible-light system. S-scheme heterojunction accelerated the photogenerated electrons to allow rapid conversion of Co(III) to Co(II), promoting the fast two-electron transfer from Co(II) to Co(IV)=O. Consequently, the developed BiOCl-OV/CoAl-LDH/PMS/Visible-light system showed excellent degradation efficiency for most of organic pollutions, and exhibited very high removal capability for the actual industrial wastewater. This study provides a new insight into the evolution of Co(IV)=O and the coordinative mechanism for photocatalysis and PMS activation.

Enhanced removing of cyanobacterium by NZVI coupled with H2O2: Influencing factors and removal mechanisms

AbstractAs advanced oxidation processes (AOPs) is considered to be a highly effective approach for degrading organic pollutants, the simultaneous coagulation and oxidation process by the Fenton‐like reaction of nanoscale zero‐valent iron (NZVI) and hydrogen peroxide (H2O2) is investigated to eliminate the harmful cyanobacterium Microcystis aeruginosa in this study, and the process conditions are optimized using the central composite design of response surface methodology (RSM); in addition, the removal efficiency of M. aeruginosa (in terms of chlorophyll a, Chl a) and the verifications of the antioxidant abilities, as well as extracellular organic matters (EOM) and intracellular organic matters (IOM) are investigated under the optimized conditions. Results indicate that H2O2 concentration is the key factor affecting the Chl a removal efficiency, and the maximum Chl a removal reaches 98.10% under the optimized conditions: NZVI concentration 62.82 mg L−1, H2O2 concentration 54.2 mmol L−1, pH 4.38 and rotating speed 67 rpm. The high correlation coefficient (R2 > 0.80) of analysis of variance (ANOVA) demonstrates the RSM model is extremely significant and suitable for experimental results. Moreover, the total organic carbon (TOC) and fluorescent substances (soluble cyanobacteria metabolic byproducts, aromatic proteins II, humic and fulvic acid‐like compounds) for both EOM and IOM are enhanced removal. It is speculated the removal mechanisms of the Fenton‐like process of NZVI/H2O2 for cyanobacterium belongs to the combined actions of the oxidation of Fe(II)/H2O2 and the coagulation of Fe(III), which destroy the defense system and result in the removal of M. aeruginosa.

Effective electro-removal of glyphosate and glufosinate from aqueous solutions via capacitive deionization

Both glyphosate (Gly) and glufosinate (Glu) are commonly used as herbicides, which has caused rising concerns about their impact on the environment and human health. Capacitive deionization (CDI) is a newly developed energy-efficient water treatment technique that effectively removes inorganic and small organic molecules under the electric field. In this work, a carbon electrode-based CDI device was used in the electro-removal of Gly and Glu in an aqueous solution with an excellent removal rate of up to 95 % under various conditions. Furthermore, maximum electro-removal rates of 1.99 μmol∙cm−2∙min−1 for Gly and 1.33 μmol∙cm−2∙min−1 for Glu were also achieved, except with super-high removal rates of 100 % (Gly) and 97.6 % (Glu) in actual Gly and Glu-containing lake water, demonstrating the feasibility of the CDI device in real aqueous systems. In-situ electro-oxidation that occurred during the electrosorption process was confirmed by analyzing the three-electrode system-based electrochemical behaviors and tracing the time-dependent changes of the suspicious degradation products. Transition state (TS) search and molecular dynamics (MD) simulations were employed to study the microscopic processes theoretically, revealing the degradation pathways and thermodynamic characteristics of Gly and Glu. This research presents a novel avenue for the decomposition and removal of herbicides from water, leveraging the inherent side reactions of CDI systems as an advantage to decontaminate organic pollutants.

Comparative study of photocatalysis with bulk and nanosheet graphitic carbon nitrides enhanced with silver

The main goal of this research is to investigate the effectiveness of graphitic carbon nitride (g-C3N4, g-CN) in both bulk and nanosheet forms, which have been surface-modified with silver nanoparticles (Ag NPs), as photocatalysts for the degradation of acid orange 7 (AO7), a model dye. The photodegradation of AO7 dye molecules in water was used to test the potential photocatalytic properties of these powder materials under two different lamps with wavelengths of 368 nm (UV light) and 420 nm (VIS light). To produce Ag NPs (Ag content 0.5, 1.5, and 3 wt%) on the g-CN materials, a new synthesis route based on a wet and low-temperature method was proposed, eliminating the need for reducing agents. The photodegradation activity of the samples increased with increasing silver content, with the best photocatalytic performances achieved for bulk g-CN samples and nanosheet silver-modified samples (with the highest content of 3 wt% Ag) under UV light, i.e., more than 75% and 78%, respectively. The VIS-induced photocatalytic activity of both examined series was higher than that of UV. The highest activities of 92% and 98% were achieved for the 1.5% Ag-modified g-CN bulk and nanosheet materials. This research presents an innovative, affordable, and environmentally friendly chemical approach to synthesizing photocatalysts that can be used for degrading organic pollutants in wastewater treatment.

The impacts of biodegradable and non-biodegradable microplastic on the performance and microbial community characterization of aerobic granular sludge

IntroductionMicroplastics (MPs), identified as emerging contaminants, have been detected across diverse environmental media. Their enduring presence and small size facilitate the adsorption of organic pollutants and heavy metals, leading to combined pollution effects. MPs also accumulate in the food chain thus pose risks to animals, plants, and human health, garnering significant scholarly attention in recent years. Aerobic granular sludge (AGS) technology emerges as an innovative approach to wastewater treatment. However, the impacts of MPs on the operational efficiency and microbial characteristics of AGS systems has been insufficiently explored.MethodsThis study investigated the effects of varying concentration (10, 50, and 100 mg/L) of biodegradable MPs (Polylactic Acid, PLA) and non-biodegradable MPs (Polyethylene Terephthalate, PET) on the properties of AGS and explored the underlying mechanisms.Results and discussionsIt was discovered that low and medium concentration of MPs (10 and 50 mg/L) showed no significant effects on COD removal by AGS, but high concentration (100 mg/L) of MPs markedly diminished the ability to remove COD of AGS, by blocking most of the nutrient transport channels of AGS. However, both PLA and PE promoted the nitrogen and phosphorus removal ability of AGS, and significantly increased the removal efficiency of total inorganic nitrogen (TIN) and total phosphorus (TP) at stages II and III (P < 0.05). High concentration of MPs inhibited the growth of sludge. PET noticeably deteriorate the sedimentation performance of AGS, while 50 mg/L PLA proved to be beneficial to sludge sedimentation at stage II. The addition of MPs promoted the abundance of Candidatus_Competibacter and Acinetobacter in AGS, thereby promoting the phosphorus removal capacity of AGS. Both 50 mg/L PET and 100 mg/L PLA caused large amount of white Thiothrix filamentous bacteria forming on the surface of AGS, leading to deterioration of the sludge settling performance and affecting the normal operation of the reactor. Comparing with PET, AGS proved to be more resistant to PLA, so more attention should be paid to the effect of non-biodegradable MPs on AGS in the future.

Preparation of MWCNT/CoMn2O4 nanocomposite for effectual degradation of picric acid via peroxymonosulfate activation

In recent years, using nanomaterials based on multi-wall carbon nanotubes (MWCNT) through the activation of peroxymonosulfate (PMS) has attracted more attention to the degradation of organic pollutants. This research presented a new route for the synthesis of MWCNT/CoMn2O4 nanocomposite for the degradation of picric acid using advanced oxidation processes (AOPs). Firstly, CoMn2O4 nanoparticles were prepared and then loaded on MWCNT using ultrasonic waves. The results of various analyzes confirmed the successful loading of nanoparticles on carbon nanotubes. As the degradation process proceeds through oxidation processes, the high electronic conductivity of MWCNT and the active sites of Mn and Co in the nanocomposite play an essential role in activating PMS to generate reactive oxygen species (ROS). An investigation of the reaction mechanism in different conditions showed that the highest speed of picric acid decomposition in the presence of nanocomposite (98%) was in 47 min. However, the scavenger test showed that HO· and SO4·− radicals are more important in the degradation process. Meanwhile, the results showed that removing picric acid using MWCNT/CoMn2O4 was more effective than CoMn2O4 alone and confirmed the interaction effect of MWCNT nanotubes with AB2O4 nanocatalyst.

Effectiveness of chemical oxygen demand as an indicator of organic pollution in aquatic environments

Effectiveness of chemical oxygen demand as an indicator of organic pollution in aquatic environments

BiOClxM1-x (M=I, Br) solid solution-coupled CdS photocatalysts for enhanced visible light-driven organic pollutants degradation with simultaneous hydrogen production

The construction of Z-scheme heterojunction stands out as one of the most effective modification methods for enhancing the performance of photocatalysts. Therefore, BiOClxM1-x (M=I, Br) solid solution-coupled CdS (BiOClxM1-x/CdS) Z-scheme photocatalysts were successfully synthesized by a hydrothermal-precipitation method. BiOCl0.8I0.2/CdS exhibited notable photocatalytic performance with a hydrogen yield of 261 μmol/g, which was 2.23, 1.56 and 1.44 times higher than that of CdS, BiOCl/CdS and BiOCl0.5Br0.5/CdS, respectively. This improvement can be attributed to two key factors: (1) the formation of BiOClxM1-x (M=I, Br) solid solution enhances visible light absorption; (2) The formation of BiOCl0.8I0.2/CdS (M=I, Br) Z-scheme heterojunctions inhibit the recombination of photogenerated carriers to prolong the lifetime of photogenerated carriers, thus increasing the utilization of the photogenerated carriers. Moreover, BiOCl0.8I0.2/CdS also showed good photocatalytic activity in ROW-DFHP (residual organic wastewater from dark fermentation for hydrogen production), with a hydrogen production rate of 42.83 μmol/g and a mineralization rate of organic pollutants of 31.73%. Cycling experiments, XRD and SEM of the samples before and after the photocatalytic reaction showed that BiOCl0.8I0.2/CdS has good stability. Furthermore, the mechanism of BiOCl0.8I0.2/CdS for the photocatalytic degradation of organic pollutants and simultaneous hydrogen production was proposed, offering a novel strategy for organic wastewater purification and hydrogen energy recovery.

The catalytic hydro-dechlorination of 2, 4, 4’ trichlorobiphenyl at mild temperatures and atmospheric pressure

ABSTRACT Polychlorinated biphenyls (PCBs), including all 209 congeners, are designated as persistent organic pollutants (POPs) due to their high toxicity and bioaccumulation in human bodies and the ecosystem. The need for PCB remediation still remains long after their production ban. In this study, a catalytic hydro-dechlorination (HDC) method was employed to dechlorinate 2,4,4’-trichlorobiphenyl (PCB 28), a congener found ubiquitously in multiple environmental media. The HDC of PCB 28 was experimentally studied at mild temperatures viz. ~20, 50, and ~ 77°C and atmospheric pressure. Et3N (triethylamine) was added as a co-catalyst. The dechlorination rates increased with temperature as well as Et3N dosage, and the HDC pathway was hypothesized based on the product and intermediates observed. The less chlorinated intermediates suggested that the position of the chlorine strongly impacted HDC rates, and the preference of HDC at para positions can be orders of magnitudes higher than the ortho. The activation energy, was estimated in the range of 12.4-13.9 kJ/mole, indicating a diffusion-controlled HDC system. Implication Statement The remediation need for polychlorinated biphenyls (PCBs) still remains long after their production ban around the world. The development of low cost methods is highly desirable, especially for developing countries, in response to the Stockholm Convention. In this study, the dechorination of a ubiquitously present PCB congener was studied using a catalytic hydro-dechlorination (HDC) method in low temperatures up to ~ 77°C and was able to achieve near 100% dechlorination in six hours. Results indicated that the HDC process can be performed under mild temperatures and atmospheric conditions and can be a potential solution to real world PCB contamination issues.

Environmental transformation and hazards of decachlorobiphenyl on suspended particles under sunlight irradiation.

Decachlorobiphenyl (PCB-209) can be widely detected in suspended particles and sediments due to its large hydrophobicity, and some of its transformation products may potentially threaten organisms through the food chain. Here we investigate the photochemical transformation of PCB-209 on suspended particles from the Yellow River. It was found that the suspended particles had an obvious shielding effect to largely inhibit the photodegradation of PCB-209. Meanwhile, the presence of inorganic ions (e.g. Mg2+ and NO3-) and organic matters (e.g. humic acid, HA) in the Yellow River water inhibited the reaction. The main transformation products of PCB-209 were lower-chlorinated and hydroxylated polychlorinated biphenyls (OH-PCBs), and small amounts of pentachlorophenol (PCP) and polychlorinated dibenzofurans (PCDFs) were also observed. The mechanisms of PCP formation by double •OH attacking carbon bridge and PCDFs formation by elimination reaction of ionic state OH-PCBs were proposed using theoretical calculations, which provided some new insights into the inter-transformations between persistent organic pollutants. In combination with VEGA and EPI Suite software, some intermediates such as PCDFs were more toxic to organisms than PCB-209. This study deepens the understanding of the transformation behavior of PCB-209 on suspended particles under sunlight.