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.

The present work evaluates the action of nitroreductase enzyme immobilized on Tosylactivated magnetic particles (MP-Tosyl) on three disperse dyes which contain nitro and azo groups. The dyes included Disperse Red 73 (DR 73), Disperse Red 78 (DR 78), and Disperse Red 167 (DR 167). The use of a magnet enabled the rapid and easy removal of the immobilized enzyme after biotransformation; this facilitated the identification of the products generated using high-performance liquid chromatography with diode array detector (HPLC-DAD) and mass spectrometry (LC-MS/MS). The main products formed by the in vitro biotransformation were identified as the product of nitro group reduction to the correspondent amine groups, which were denoted as follows: 50% of 2-(2-(4-((2-cyanoethyl)(ethyl)amino)phenyl)hydrazinyl)-5-nitrobenzonitrile, 98% of 3-((4-((4-amino-2-chlorophenyl) diazenyl)phenyl) (ethyl)amino)propanenitrile and 99% of (3-acetamido-4 - ((4-amino-2-chlorophenyl) diazenyl) phenyl) azanediyl) bis (ethane-2,1-diyl) for DR 73, DR 78 and DR 167, respectively. Based on the docking studies, the dyes investigated were found to be biotransformed by nitroreductase enzyme due to their favorable interaction with the active site of the enzyme. Theoretical results show that DR73 dye exhibits a relatively lower rate of degradation; this is attributed to the cyanide substituent which affects the electron density of the azo group. The docking studies also indicate that all the dyes presented significant reactivity towards DNA. However, Disperse Red 73 was found to exhibit a substantially higher reactivity compared to the other dyes; this implies that the dye possesses a relatively higher mutagenic power. The docking results also show that DR 73, DR 78 and DR 167 may be harmful to both humans and the environment, since the mutagenicity of nitro compounds is associated with the products formed during the reduction of nitro groups. These products can interact with biomolecules, including DNA, causing toxic and mutagenic effects.

Organic contaminants deposited on glacier snow and ice are subject to partitioning and degradation processes that determine their environmental fate and, consequently, their accumulation in ice bodies. Among these processes, organic compound metabolism by supraglacial bacteria has investigated to a lesser extent than photo- and chemical degradation. We investigated biodegradation of the organophosphorus insecticide chlorpyrifos (CPF), a xenobiotic tracer that accumulates on glaciers after atmospheric medium- and long-range transport, by installing in situ microcosms on an Alpine glacier to simulate cryoconite hole systems. We found that biodegradation contributed to the removal of CPF from the glacier surface more than photo- and chemical degradation. The high concentration of CPF (2–3 μg g−1 w.w.) detected in cryoconite holes and the estimated half-life of this compound (35–69 days in glacier environment) indicated that biodegradation can significantly reduce CPF concentrations on glaciers and its runoff to downstream ecosystems. The metabolic versatility of cryoconite bacteria suggests that these habitats might contribute to the degradation of a wide class of pollutants. We therefore propose that cryoconite acts as a “biofilter” by accumulating both pollutants and biodegradative microbial communities. The contribution of cryoconite to the removal of organic pollutants should be included in models predicting the environmental fate of these compounds in cold areas.

Plastic ingestion has been widely investigated to understand its adverse harms on fauna, but the role of fauna itself in plastic fragmentation has been rarely addressed. Here, we review and discuss the available experimental results on the role of terrestrial and aquatic macrofauna in plastic biofragmentation and degradation. Recent studies have shown how biting, chewing, and stomach contractions of organisms shatter ingested plastic along their digestive tracts. Gut microbial communities can play a role in biodegradation and their composition can shift according to the type of plastic ingested. Shifts in molecular weights, chemical bond forming and breaking, and changes in thermal modification detected in the plastic debris present in the faeces also suggest active biodegradation. A few studies have also shown interactions other than ingestion, such as burrowing, may actively or passively promote physical plastic fragmentation by fauna. We suggest that further investigations into the role of fauna in physical fragmentation and chemical degradation linked to active ingestion and gut associated microbiota metabolism, respectively, should be conducted to better evaluate the impact of these mechanisms on the release of micro- and nano-plastic in the environment. Knowledge on macrofauna other than marine invertebrates and terrestrial soil dwelling invertebrates is particularly lacking, as well as focus on broader types of plastic polymers.

Antibiotic residues in the environment are concerning since results in dispersion of resistance genes. Their degradation is often closely related to microbial metabolism. However, the impacts of soil bacterial community on sulfadiazine (SDZ) dissipation remains unclear, mainly in tropical soils. Our main goals were to evaluate effects of long-term swine manure application on soil bacterial structure as well as effects of soil microbial diversity depletion on SDZ dissipation, using “extinction dilution approach” and ¹⁴C-SDZ. Manure application affected several soil attributes, such as pH, organic carbon (OC), and macronutrient contents as well as bacterial community structure and diversity. Even minor bacterial diversity depletion impacted SDZ mineralization and non-extractible residue (NER) formation rates, but NER recovered along 42 d likely due to soil diversity recovery. However, this period may be enough to spread resistance genes into the environment. Surprisingly, the non-manured natural soil (NS–S1) showed faster SDZ dissipation rate (DT₉₀ = 2.0 versus 21 d) and had a great number of bacterial families involved in major SDZ dissipation pathways (mineralization and mainly NER), such as Isosphaeraceae, Ktedonobacteraceae, Acidobacteriaceae_(Subgroup_1), Micromonosporaceae, and Sphingobacteriaceae. This result is unique and contrasts our hypothesis that long-term manured soils would present adaptive advantages and, consequently, have higher SDZ dissipation rates. The literature suggests instantaneous chemical degradation of SDZ in acidic soils responsible to the fast formation of NER. Our results show that if chemical degradation happens, it is soon followed by microbial metabolism (biodegradation) performed by a pool of bacteria and the newly formed metabolites should favors NER formation since SDZ presented low sorption. It also showed that SDZ mineralization is a low redundancy function.

Bisphenol A, bisphenol S, and fluconazole are ubiquitous environmental pollutants and their removal from water is of utmost importance. As the biodegradation of these compounds is usually not enough effective, often other degradation methods are required. The study presents the difference between biodegradation and photo-Fenton degradation with a much higher efficiency obtained in the latter process. Levels of biodegradation and chemical degradation were assessed based on high-performance liquid chromatography determination. Optimization of the photo-Fenton removal of bisphenol A, bisphenol S, and fluconazole resulted in about 100 % primary degradation of both bisphenols during 10–20 min and almost 90 % primary degradation of fluconazole within an hour. Degradation products formed in the process were identified using liquid chromatography with mass spectrometry and showed central scission of bisphenol S with the formation of phenol and sulfuric acid while for bisphenol A and fluconazole the oxidation resulted in much smaller structural changes.

Investigations of the physicochemical degradation of personal protective equipment (PPE) under controlled environmental conditions are largely lacking. Here the chemical and physical changes of face masks and gloves (recovered from the marine environment) were evaluated after exposure time up to 60 days of simulated environmental conditions. The results suggested that the polymer backbone of PPE suffers typical changes induced by sun exposure. Changes in the intensity of diffraction peaks indicated shifts in the crystallinity of PPE, possibly altering their thermal behavior. Signs of physical degradation in PPE, such as ruptures, and rough surfaces, which exacerbated over time were also detected. Additionally, signals of some elements of concern, such as Cu and Mo, and elements typically found in seawater were detected. The results of this study allowed us to better understand the degradation of typical PPE items in the marine environment, ultimately resulting in the release of microplastics and chemical contaminants.

In this article we compare the efficiency of different methods of rapid-response remediation of beach sand contaminated with microbiological and/or organic matter. Contaminated beach sands were treated in laboratory by different treatment methods (i.e., oxidation, UV-photoexposure, or thermal methods) and the efficiency of disinfection and breakdown of organic matter were evaluated. Contaminants in raw and treated beach sands were measured by membrane filtration method, and by chemical and biochemical oxygen demand, and chromatographic analysis. All the methods tested were efficient for disinfecting beach sand with microbiological contamination, except for the UV-photoexposure method, which showed only moderate disinfection potential. Chemical degradation efficiency of beach sand contaminated by crude petroleum was higher with Fenton and Photo-Fenton (associated with the use of surfactant and ultrasound) methods. Photo-Fenton method improvement can increase the efficiency of contaminated beach sand treatment, and can also help beach managers when selecting which method to adopt for remedial actions.

During typesetting, the image of figure 4 was also used in figure 5. The mistake was discovered after the original article was published online.

Degradation and fate of sulfamethazine (SMZ) were determined under aerobic and anaerobic conditions in soil with and without swine manure amendment. For both aerobic and anaerobic conditions, SMZ disappeared rapidly during the first 7 days followed by slow disappearance which may indicate that SMZ had become more persistent and less available. For soils receiving 100 mg/kg of SMZ, the percent of SMZ remaining in the soil after 63 days were between 25 and 60 %. Depending on the initial SMZ concentration, estimated half-lives for aerobic and anaerobic incubations ranged from 1.2 to 6.6 and 2.3 days to more than 63 days, respectively. Addition of manure (0.054 g/g soil) did not significantly affect the half-lives of SMZ. Inhibitory effects of SMZ on anaerobic microbial respiration were observed in unamended soil at concentrations of 50 mg/kg or higher, but only transient inhibitory effects were found in aerobic soil. Five to 22 % of the¹⁴C[phenyl]-SMZ added were extracted at the end of the incubations while 70 to 91 % of the¹⁴C were converted to bound (non-extractable) forms in both manure amended and unamended soil. Only 0.1 to 1.5 % of¹⁴C-SMZ was mineralized to¹⁴CO₂. Disappearance of SMZ in sterilized soil was not completely halted indicating possible contribution of abiotic processes to the disappearance of SMZ in soil.