It is difficult to achieve simultaneous and efficient removal of heterocyclic drugs (HCDs) and total nitrogen (TN) in conventional denitrification biofilter (DNBF). Inspired by the effective degradation of refractory organic matter by cobalt-based advanced oxidation process and the need for in-situ upgrading of DNBF, peracetic acid (PAA)/cobalt-loaded ceramsite-based DNBF system was constructed for the first time to treat biochemical tailwater containing HCDs. Results showed that PAA/Co-DNBF had relatively high removal rates for the four HCDs with the order of CBZ > TMP > SDZ > SMX, and the optimal DNBF was H2 with 150 μg L⁻¹of PAA. Overall, TN and HCDs removal increased by 178%–455% and 2.50%–40.99% respectively. When the influent concentration of NO₃⁻-N, COD and each HCDs of 20 mg/L, 60 mg/L and 20 μg/L, below 15 mg/L of effluent TN and the highest average removal rate of SMX (67.77%) could be achieved, under HRT of 4 h in H2. More even distribution of microbial species and low acute toxicity of effluent were also achieved. More even distribution of microbial species and low acute toxicity of effluent were also achieved. In addition, high extracellular polymeric substance (EPS) content and Gordonia after the addition of PAA contributed to the degradation of HCDs. This study supplied a potentially effective strategy for the treatment of biochemical tailwater containing HCDs and provided new insight into the advance of denitrification technology.

Rising global demand for energy promotes extensive mining of natural resources, such as oil sands extractions in Alberta, Canada. These extractive activities release hazardous chemicals into the environment, such as polycyclic aromatic compounds (PACs), which include the parent polycyclic aromatic hydrocarbons (PAHs), alkylated PAHs, and sulfur-containing heterocyclic dibenzothiophenes (DBTs). In areas adjacent to industrial installations, Indigenous communities may be exposed to these PACs through the consumption of traditional foods. Our objective was to evaluate and compare the concentrations of total PACs (∑PAC), expressed as the sum of the 16 U.S. EPA priority PAHs (∑PAH), 49 alkylated PAHs (∑alkyl-PAH), and 7 DBTs (∑DBT) in plant and animal foods collected in 2015 by the Bigstone Cree Nation in Alberta, Canada. We analyzed 42 plant tissues, 40 animal muscles, 5 ribs, and 4 pooled liver samples. Concentrations of ∑PAC were higher in the lichen, old man’s beard (Usnea spp.) (808 ± 116 ng g⁻¹ w.w.), than in vascular plants, and were also higher in smoked moose (Alces alces) rib (461 ± 120 ng g⁻¹ w.w.) than in all other non-smoked animal samples. Alkylated-PAHs accounted for between 63% and 95% of ∑PAC, while the concentrations of ∑PAH represented 4%–36% of ∑PAC. Contributions of ∑DBT to ∑PAC were generally lowest, ranging from <1% to 14%. While the concentrations of benzo(a)pyrene (B[a]P) and ∑PAH4 (∑benzo[a]anthracene, chrysene, benzo[b]fluoranthene, and B[a]P) in all samples were below guideline levels for human consumption as determined by the European Commission, guideline levels for the more prevalent alkylated PAHs are not available. Given the predominance of alkylated PAHs in all food samples and the potentially elevated toxicity relative to parent PAHs of this class of PACs, it is critical to consider a broader range of PACs other than just parent PAHs in research conducted close to oil sands mining activities.

Groundwater serves as a main drinking water source for rural residents in China. However, little is known regarding the pollution of organic micropollutants in groundwater that may pose health risks. In this study, more than 1300 organic micropollutants were screened in the groundwater samples collected from 13 drinking water wells distributed across five rural regions of Liaodong Peninsula in China. A total of 80 organic micropollutants including 12 polycyclic aromatic hydrocarbons, 11 alkanes, 9 pesticides, 7 substituted phenols, 7 perfluoroalkyl acids, 6 heterocyclic compounds, 5 alcohols, 5 phthalic acid esters, 5 pharmaceutical and personal care products, 3 ketones, 2 polychlorinated biphenyls (PCBs), 2 alkylbenzenes and 2 chlorinated benzenes were detected, with their total concentration of 32–1.5 × 104 ng/L. Noncarcinogenic and carcinogenic risks of a part of pollutants were assessed. Exposure through skin absorption and oral ingestion was considered in the assessment. Generally the risks are within the acceptable limits, except for that the carcinogenic risk at two sites in Jinzhou is higher than 10−6. To the best of our knowledge, this is the first report on health risks of groundwater micropollutants in China.

Hexanitrohexaazaisowurtzitane (CL-20) is an emerging explosive that may replace the currently used explosives such as RDX and HMX, but little is known about its fate in soil. The present study was conducted to determine degradation products of CL-20 in two sandy soils under abiotic and biotic anaerobic conditions. Biotic degradation was prevalent in the slightly acidic VT soil, which contained a greater organic C content, while the slightly alkaline SAC soil favored hydrolysis. CL-20 degradation was accompanied by the formation of formate, glyoxal, nitrite, ammonium, and nitrous oxide. Biotic degradation of CL-20 occurred through the formation of its denitrohydrogenated derivative (m/z 393 Da) while hydrolysis occurred through the formation of a ring cleavage product (m/z 156 Da) that was tentatively identified as CH2N-C(N-NO2)-CHN-CHO or its isomer N(NO2)CH-CHN-CO-CHNH. Due to their chemical specificity, these two intermediates may be considered as markers of in situ attenuation of CL-20 in soil. Two key intermediates of CL-20 degradation are potential markers of its natural attenuation in soil.

Zerovalent iron (Fe0, ZVI) has drawn great interest as an inexpensive and effective material to promote the degradation of environmental contaminants. A focus of ZVI research is to increase degradation kinetics and overcome passivation for long-term remediation. Halide ions promote corrosion, which can increase and sustain ZVI reactivity. Adding chloride or bromide salts with Fe0 (1% w/v) greatly enhanced TNT, RDX, and HMX degradation rates in aqueous solution. Adding Cl or Br salts after 24 h also restored ZVI reactivity, resulting in complete degradation within 8 h. These observations may be attributed to removal of the passivating oxide layer and pitting corrosion of the iron. While the relative increase in degradation rate by Cl- and Br- was similar, TNT degraded faster than RDX and HMX. HMX was most difficult to remove using ZVI alone but ZVI remained effective after five HMX reseeding cycles when Br- was present in solution. The addition of halide ions promotes the degradation of high explosives by zerovalent iron.

Gasification is the thermo-chemical process that converts biomass into producer gas which is used for various applications like heat production, electricity, and hydrocarbon synthesis. In this present work, the steam gasification of biomedical waste such as glucose plastic bottle, syringe, and Indian palm kernel shell is gasified in fluidized bed gasifier. The mixture of palm kernel shell co-feeding with biomedical waste such as 100% palm kernel shell (PKS), 25% biomedical waste (BMW), 50% biomedical waste, and 100% biomedical waste using olivine as a primary catalyst is used. The influences of co-feeding of biomedical waste with palm kernel shell on the gas yield, char yield, tar yield, carbon conversion efficiency, tar composition, and gas composition are investigated. The co-feeding of biomedical waste with palm kernel shell for steam/feedstock mass ratio of 1, the tar content is decreased from 53.56 to 3.6 gNm⁻³ and the char is reduced from 4.9 to 0.4 wt %. Heterocyclic, heavy polycyclic aromatic hydrocarbons and light aromatic compounds are reducing when compared to that of light polycyclic aromatic hydrocarbons at temperature 900 °C. The value of carbon conversion efficiency also increases for palm kernel shell is 78.7% and for biomedical waste is 98% respectively. Hence, the scope of the present study is to optimize the process parameters for the taken feedstock with respect to our environmental condition with the help of lab scale reactors. Later scale up can be done to utilize the product for practical applications.

This study aimed at investigating the photochemical behavior of sulfa drugs containing five and six-membered heterocyclic substituents (sulfamethoxazole (SMX) and sulfadiazine (SDZ), respectively), in an aqueous medium. Despite their importance, studies devoted to the use of photochemical models to predict the environmental phototransformation of pollutants in surface waters, by combining laboratory results and natural aquatic systems parameters, are still scarce in the scientific literature. In this work, the second-order reaction rate constants of SDZ and SMX with hydroxyl radicals (●OH), singlet oxygen (¹O₂), and triplet excited states of chromophoric dissolved organic matter (³CDOM*) were experimentally determined at pH 7, using the competition kinetics approach. The results show that ●OH and ³CDOM* are the key species involved in sulfonamide degradation, with anionic SMX, most prevalent at pH 6–9, being degraded much slower than the anionic form of SDZ. Moreover, SDZ and SMX photodegradation in natural water samples (spring-fed natural pond, public supply reservoir, and sea water) was significantly enhanced relative to depletion in pure water. Finally, from mathematical simulations of the sunlight-driven sulfonamide degradation, half-life times were predicted for these drugs varying from less than 2 to about 90 days, depending on the water depth, concentration of key species (DOC, HCO₃⁻, NO₂⁻, CO₃²⁻) in natural aqueous systems, as well as on the particular heterocyclic substituent.

A green methodology was developed for the analysis of ten heterocyclic aromatic amines (HAAs) in biomass samples from cigarette combustion such as mainstream smoke, paper ashes, as well as tobacco and paper wraps. The cellulose filter used for sample collection was also evaluated. This strategy was based on ultrasound-assisted extraction (UAE) associated with a solid-phase extraction procedure employing multi-walled carbon nanotubes (MWCNTs-SPE) as a cleanup step followed by ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). Under optimal experimental conditions, the linearity of the method was in the range from 0.08 to 160 ng cig⁻¹, with correlation coefficients (R²) higher than 0.991. The limits of detection resulted to be between 0.03 and 0.63 ng cig⁻¹. Concentrations of the HAAs in the mainstream smoke were from 5.7 to 145.2 ng cig⁻¹ and in paper ashes from 0.1 to 0.6 ng cig ⁻¹, while in tobacco were between 1.0 and 38.5 ng cig⁻¹. Meanwhile, no HAA contribution was observed in the case of paper wraps and the filter used for sample collection. The knowledge of the presence and the concentration levels of the selected HAAs in each cigarette’s physical component after its combustion is essential to understand the formation processes and contribution during cigarette burning. Besides, this is the first report about the presence of some HAAs in the proposed samples. Finally, a comparative study was employed to classify the sustainability of several recent approaches for HAA extraction from cigarette combustion samples using Green Certificate as a metric tool.

Sulfadiazine (SDZ) was effectively removed by the heterogeneous catalytic sulfate radical (SO₄•⁻) oxidation using a novel composite material of mesoporous carbon (MC) loaded nano zero-valent iron (nZVI). Possessing larger specific area (433.3 m² g⁻¹) and high mesopores volume (2.537 cm³ g⁻¹), the composite material (nZVI/MC) was used as the activator to activate persulfate for the degradation of SDZ. The results of degradation experiments indicated that the removal efficiency of SDZ in nZVI/MC+ persulfate (PS) process reached the highest, due to good dispersing property of MC for nZVI. The removal of SDZ was further enhanced by the increase of nZVI loading as well as the nZVI/MC composite content. Quenching experiments showed that SO₄•⁻ acted a crucial role in the degradation process of SDZ. Both the FT-IR and XPS analyses showed that the FeO contents decreased after degradation reaction, which indicated the occurrence of active oxidation reaction between SO₄•⁻ and Fe²⁺ from the breakage of the Fe–O bond. The LC-MS analysis indicated that the cleavages of C–N bond in the heterocyclic ring and N–S bond were the major degradation pathway of SDZ, attributing to the attack of SO₄•⁻ and •OH. These results demonstrated that the novel nZVI/MC composite with excellent stability could be used for the effective degradation of SDZ through activating PS to produce SO₄•⁻. Graphical Abstract

Coal carbonization by-products contain up to 10,000 aliphatic and aromatic compounds. Many of them show toxic, mutagenic, and carcinogenic character. In this study, we examined 51 pure bacterial cultures of their ability of coal tar constituent biodegradation. Bacterial cultures were isolated from both explosives and coal tar-contaminated areas. Among all of the investigated strains, 19 showed biodegradative activity. One of the isolates degraded 40% of the substrate in 14 days at a temperature of 15°C. The most active strain was identified by both classic and 16S ribosomal DNA sequencing methods and designated Rhodococcus erythropolis B10. The biodegradation of coal tar constituents, performed by identified strain, was assessed by GC/MS technique. The comparison of samples analyzed by GC/MS before and after biodegradation indicated high degradative potential of the chosen strain. It was able to degrade n-paraffins, n-olefins, benzene, alkylbenzenes, cadalene, and other PAHs, as well as recalcitrant heterocyclic compounds dibenzofuran and its methyl-substituted derivative. The B10 strain isolated and tested in this research shows promising possibilities to be used in field conditions. The biodegradation experiments indicated that satisfactory results may be obtained even in pure bacterial cultures.