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To better characterize properties governing the sorption of per- and polyfluoroalkyl substances (PFAS) to biochar, twenty-three diverse biochars were characterized and evaluated as sorbents for perfluorooctanoic acid (PFOA). Biochars were produced at various temperatures, using two different technologies, and made from sewage sludge, food waste reject, wood wastes, and one reference substrate (wood pellets). The biochars were characterized in terms of surface area, pore volume and pore size distributions, elemental composition, leachable elements, ash content, pH, zeta potential, condensed aromatic carbon (ConAC) content (determined by benzenepolycarboxylic acid (BPCA) markers), and their -OH functional group content (infrared spectroscopy). PFOA sorption isotherms were determined using Polanyi-Dubinin-Manes (PDM) and Freundlich models. The sludge-based biochars [Freundlich coefficients (log K F ) between 2.56 ± 0.11 and 6.72 ± 0.22 (μg/kg)/(μg/L) nF ; fitted free energy of adsorption (E) and pore volume (V o ) from the PDM model between 13.27 and 17.26 kJ/mol, and 0.50 and 523.51 cm 3 /kg] outperformed wood biochars [log K F between 1.02 and 4.56 ± 0.22 (μg/kg)/(μg/L) nF ; E between 9.87 and 17.44 kJ/mol; V o between 0.21 and 7.16 cm 3 /kg] as PFOA sorbents. Multivariate statistical analysis revealed that the sorption capacity was mainly controlled by pore volume within the pore diameter region that could accommodate the molecular size of PFOA (3-6 nm). Hydrophobic interactions between PFOA and aromatic carbon rich regions controlled sorption affinity, especially in the wood biochars., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)

Biomass pyrolysis is the anoxic thermal conversion of biomass into a carbon rich, porous solid, often called biochar. This could be a better waste management alternative for contaminated organic wastes than incineration, due to the useful properties of biochar and potential for carbon sequestration. There are, however, concerns about the potential formation/destruction of polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs) and polychlorinated dibenzo-p-dioxins and furans (PCDD/Fs). Six organic wastes, including digested sewage sludges, wood wastes, and food waste reject, were pyrolyzed (500-800°C) in a full-scale relevant unit (1-5 kg biochar hr -1 ). Removal efficiencies for PCBs and PCDD/Fs were > 99% in the produced biochars. Biochar PAH-content (2.7-118 mgkg -1 ) was not significantly correlated to feedstock or temperature. PAHs (2563-8285 mgkg -1 ), PCBs (22-113 µgkg -1 ), and PCDD/Fs (1.8-50 ngTEQ kg -1 ) accumulated in the pyrolysis condensate, making this a hazardous waste best handled as a fuel for high temperature combustion. Emission concentrations for PAHs (0.22-421 µgNm -3 ) and PCDD/Fs (≤2.7 pgTEQ Nm -3 ) were mainly associated with particles and were below the European Union's waste incineration thresholds. Emission factors ranged from 0.0002 to 78 mg tonne -1 biochar for PAHs and 0.002-0.45 µgTEQ tonne -1 biochar for PCDD/Fs. PCDD/F-formation was negligible during high temperature (≥500 °C) biomass pyrolysis (69-90% net loss)., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.)

Biochars are considered potential sustainable sorbents to reduce the leaching of per- and polyfluoroalkyl substances (PFAS) from contaminated soils. However, biochar characteristics must probably be optimized to achieve useful sorption capacity. In the present work, eight waste timber biochars were produced, including biochars activated to different degrees, at different temperatures, and using both steam and CO 2 . In laboratory batch experiments, the eight biochars were amended to soil samples from two different horizons, with low and high total organic carbon (TOC, 1.6% and 34.2%, respectively), of a heavily PFAS-contaminated soil (1200-3800 μg kg -1 PFAS tot ), at varying doses (0, 0.1, 0.5, 1.0 and 5.0%). With a 5% amendment to the low-TOC soil, all eight biochars resulted in strongly reduced leachate PFAS concentrations (by 98-100%). At the same amendment dose in the high-TOC soil, leachate concentration reductions were more modest (23-100%). This was likely due to a strong PFAS-sorption to the high-TOC soil itself, as well as biochar pore clogging in the presence of abundant organic matter, resulting in fewer sorption sites available to PFAS. Reduction in PFAS leaching was proportional to the degree of activation and activation temperature. Thus, lower amendment doses of activated biochars were needed to reduce PFAS leaching to the same level as with the non-activated biochar. Activation however, came at a tradeoff with biochar yield. Furthermore, the adsorption ability of these biochars increased proportionally with PFAS-fluorocarbon chain length, demonstrating the role of hydrophobic interactions in reduction of PFAS leaching. Development of internal surface area and porosity was proposed as the main factor causing the improved performance of activated biochars. This study shows that woody residues such as waste timber can be used to produce effective sorbents for the remediation of PFAS-contaminated soil. It also highlights the desirability of sorbate and matrix-specific optimization of biochar production., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 The Author(s). Published by Elsevier B.V. All rights reserved.)

The aim of the present study was to evaluate the secondary ecotoxicological effects of soil amendment materials that can be added to contaminated soils in order to sequester harmful pollutants. To this end, a nonpolluted agricultural soil was amended with 0.5, 2, and 5% of the following four amendments: powder activated carbon (PAC), granular activated carbon, corn stover biochar, and ferric oxyhydroxide powder, which have previously been proven to sequester pollutants in soil. The resulting immediate effects (i.e., without aging the mixtures before carrying out tests) on the springtail Folsomia candida, the earthworm species Aporectodea caliginosa and Eisenia fetida, the marine bacteria Vibrio fischeri, a suite of ten prokaryotic species, and a eukaryote (the yeast species Pichia anomalia) were investigated. Reproduction of F. candida was significantly increased compared to the unamended soil when 2% biochar was added to it. None of the treatments caused a negative effect on reproduction. All amendments had a deleterious effect on the growth of A. caliginosa when compared to the unamended soil, except the 0.5% amendment of biochar. In avoidance tests, E. fetida preferred biochar compared to all other amendments including the unamended soil. All amendments reduced the inhibition of luminescence to V. fischeri, i.e., were beneficial for the bacteria, with PAC showing the greatest improvement. The effects of the amendments on the suite of prokaryotic species and the eukaryote were variable, but overall the 2% biochar dose provided the most frequent positive effect on growth. It is concluded that the four soil amendments had variable but never strongly deleterious effects on the bacteria and invertebrates studied here during the respective recommended experimental test periods.

The aim of the present study was to determine the toxicity of a mixture containing the biocides picoxystrobin, esfenvalerate, and triclosan to the reproduction and adult survival of two consecutive generations of Eisenia fetida (Savigny, 1826). Concentration addition and independent action were used to predict mixture toxicity. Due to degradation of mixture components during the course of the experiment, predictions were based both on the mixture composition at the beginning and the end of the exposure period. As degradations were dose-dependent, none of the calculated predictions were precise for the entire concentration range, although combining both predictions led us to conclude that lethal toxicity was well predicted by concentration addition and sublethal toxicity by independent action. Reproduction of the F1 generation was inhibited more (p < 0.0001) than reproduction of the F0 generation. Adult survival did not differ between generations. The accuracy of the mixture toxicity predictions thus depended on both the time-dependent mixture composition and the earthworm generation. The results of this study underline the need for more advanced mixture toxicity prediction models that consider degradation kinetics and changes in toxic effects over time., (Copyright © 2013 SETAC.)

A field lysimeter study was carried out to investigate whether the amendment of 2% powder and granular activated carbon (PAC and GAC) to a soil with moderate PAH contamination had an impact on the PAH bioaccumulation of earthworms and plants, since AC is known to be a strong sorbent for organic pollutants. Furthermore, secondary effects of AC on plants and earthworms were studied through growth and nutrient uptake, and survival and weight gain. Additionally, the effect of AC amendments on soil characteristics like pH, water holding capacity, and the water retention curve of the soil were investigated. Results show that the amendment of 2% PAC had a negative effect on plant growth while the GAC increased the growth rate of plants. PAC was toxic to earthworms, demonstrated by a significant weight loss, while the results for GAC were less clear due to ambiguous results of a field and a parallel laboratory study. Both kinds of AC significantly reduced biota to soil accumulation factors (BSAFs) of PAHs in earthworms and plants. The GAC reduced the BSAFs of earthworms by an average of 47 ± 44% and the PAC amendment reduced them by 72 ± 19%. For the investigated plants the BSAFs were reduced by 46 ± 36% and 53 ± 22% by the GAC and PAC, respectively., (Copyright © 2012 Elsevier Ltd. All rights reserved.)

Activated carbon (AC) amendment is an innovative method for the in situ remediation of contaminated soils. A field-scale AC amendment of either 2% powder or granular AC (PAC and GAC) to a PAH contaminated soil was carried out in Norway. The PAH concentration in drainage water from the field plot was measured with a direct solvent extraction and by deploying polyoxymethylene (POM) passive samplers. In addition, POM samplers were dug directly in the AC amended and unamended soil in order to monitor the reduction in free aqueous PAH concentrations in the soil pore water. The total PAH concentration in the drainage water, measured by direct solvent extraction of the water, was reduced by 14% for the PAC amendment and by 59% for GAC, 12 months after amendment. Measurements carried out with POM showed a reduction of 93% for PAC and 56% for GAC. The free aqueous PAH concentration in soil pore water was reduced 93% and 76%, 17 and 28 months after PAC amendment, compared to 84% and 69% for GAC. PAC, in contrast to GAC, was more effective for reducing freely dissolved concentrations than total dissolved ones. This could tentatively be explained by leaching of microscopic AC particles from PAC. Secondary chemical effects of the AC amendment were monitored by considering concentration changes in dissolved organic carbon (DOC) and nutrients. DOC was bound by AC, while the concentrations of nutrients (NO(3), NO(2), NH(4), PO(4), P-total, K, Ca and Mg) were variable and likely affected by external environmental factors., (Copyright © 2012 Elsevier Ltd. All rights reserved.)

A combined soil amendment was tested in microcosm experiments with an aim to enhance the aerobic biodegradation of propylene glycol (PG)-based aircraft de-icing fluids during and following the infiltration of contaminated snowmelt. A key objective under field conditions is to increase degradation of organic pollutants in the surface soil where higher microbial activity and plant rhizosphere effects may contribute to a more efficient biodegradation of PG, compared to subsoil ground layers, where electron acceptors and nutrients are often depleted. Microcosm experiments were set up in Petri dishes using 50 g of soil mixed with appropriate additives. The samples contained an initial de-icing fluid concentration of 10,000 mg/kg soil. A combined amendment using calcium peroxide, activated carbon and 1 x Hoagland solution resulted in significantly higher degradation rates for PG both at 4 and 22 degrees C. Most probable numbers of bacteria capable of utilizing 10,000 mg/kg de-icing fluid as a sole carbon source were about two orders of magnitude higher in the amended soil samples compared to unamended controls at both temperatures. The elevated numbers of such bacteria in surface soil may be a source of cells transported to the subsoil by snowmelt infiltration. The near-surface application of amendments tested here may enhance the growth of plants and plant roots in the contaminated area, as well as microbes to be found at greater depth, and hence increase the degradation of a contaminant plume present in the ground.

Activated carbon (AC) amendment to polluted sediment or soil is an emerging in situ treatment technique that reduces freely dissolved porewater concentrations and subsequently reduces the ecological and human health risk of hydrophobic organic compounds (HOCs). An important question is the capacity of the amended AC after prolonged exposure in the field. To address this issue, sorption of freshly spiked and native HOCs to AC aged under natural field conditions and fresh AC amendments was compared for one soil and two sediments. After 12-32 months of field aging, all AC amendments demonstrated effectiveness for reducing pore water concentrations of both native (30-95%) and spiked (10-90%) HOCs compared to unamended sediment or soil. Values of K(AC) for field-aged AC were lower than freshly added AC for spiked HOCs up to a factor of 10, while the effect was less for native HOCs. The different behavior in sorbing native HOCs compared to freshly spiked HOCs was attributed to differences in the sorption kinetics and degree of competition for sorption sites between the contaminants and pore-clogging natural organic matter. The implications of these findings are that amended AC can still be effective in sorbing additional HOCs some years following amendment in the field. Thus, a certain level of long-term sustainability of this remediation approach is observed, but conclusions for decade-long periods cannot be drawn solely based on the present study.

The influence of organic matter (OM) content on alpha-cypermethrin porewater concentrations and springtail Folsomia candida accumulation was investigated in two soils with different levels of organic matter, a forest soil with a total organic carbon (TOC) content of 5.0% (OM=11.5%) and an agricultural soil with a TOC content of 1.3% (OM=4.0%). Also, the effects of alpha-cypermethrin concentrations in soil and pore water and the influence of soil aging on springtail reproduction were investigated. Springtail reproduction was severely affected by increasing alpha-cypermethrin in soil with 1.3% TOC; the median effective concentration value (EC50) was estimated to 23.4 mg/kg (dry wt). Reproduction was only marginally affected in the soil with 5.0% TOC, and no EC50 value could be estimated. However, when expressing alpha-cypermethrin accumulation as a function of soil alpha-cypermethrin concentrations, no difference was found between the two soil types, and no additional alpha-cypermethrin uptake was observed at soil concentrations above approximately 200 mg/kg (dry wt). By using solid-phase microextraction (SPME), it could be demonstrated that alpha-cypermethrin porewater concentrations were higher in the soil with low organic matter (LOM) content than in the soil with high organic matter (HOM) content. Furthermore, a clear relationship was found between alpha-cypermethrin concentrations in springtails and porewater. Soil aging was not found to exert any effect on alpha-cypermethrin toxicity toward springtails. The study indicates that the springtail's accumulation of alpha-cypermethrin and reproduction is governed by alpha-cypermethrin porewater concentrations rather than the total alpha-cypermethrin concentration in soil., (Copyright (c) 2010 SETAC.)

Activated carbon (AC) strongly sorbs organic pollutants and can be used for remediation of soils and sediments. A method for AC quantification is essential to monitor AC (re)distribution. Since AC is black carbon (BC), two methods for BC quantification were tested for AC mixed in different soils and sediments: i) chemothermal oxidation (CTO) at a range of temperatures and ii) wet-chemical oxidation with a potassium dichromate/sulfuric acid solution. For three soils, the amount of AC was accurately determined by CTO at 375 degrees C. For two sediments, however, much of the AC disappeared during combustion at 375 degrees C, which could probably be explained by catalytic effects by sediment constituents. CTO at lower temperatures (325-350 degrees C) was a feasible alternative for one of the sediments. Wet oxidation effectively functioned for AC quantification in sediments, with almost complete AC recovery (81-92%) and low remaining amounts of native organic carbon (5-16%).

Organic pollutants (e.g. polyaromatic hydrocarbons (PAH)) strongly sorb to carbonaceous sorbents such as black carbon and activated carbon (BC and AC, respectively). For a creosote-contaminated soil (Sigma15PAH 5500 mg kg(dry weight(dw))(-1)) and an urban soil with moderate PAH content (Sigma15PAH 38 mg kg(dw)(-1)), total organic carbon-water distribution coefficients (K(TOC)) were up to a factor of 100 above values for amorphous (humic) organic carbon obtained by a frequently used Linear-Free-Energy Relationship. This increase could be explained by inclusion of BC (urban soil) or oil (creosote-contaminated soil) into the sorption model. AC is a manufactured sorbent for organic pollutants with similar strong sorption properties as the combustion by-product BC. AC has the potential to be used for in situ remediation of contaminated soils and sediments. The addition of small amounts of powdered AC (2%) to the moderately contaminated urban soil reduced the freely dissolved aqueous concentration of native PAH in soil/water suspensions up to 99%. For granulated AC amended to the urban soil, the reduction in freely dissolved concentrations was not as strong (median 64%), especially for the heavier PAH. This is probably due to blockage of the pore system of granulated AC resulting in AC deactivation by soil components. For powdered and granulated AC amended to the heavily contaminated creosote soil, median reductions were 63% and 4%, respectively, probably due to saturation of AC sorption sites by the high PAH concentrations and/or blockage of sorption sites and pores by oil.

Knowledge about the bioavailability and metabolism of pesticides in soil organisms facilitates interpretation of its toxicity in soil. The present study relates uptake kinetics and metabolism of two insecticides, the pyrethroid alpha-cypermethrin (alpha-CYP) and the organophosphate chlorfenvinphos (CFVP), in the earthworm Eisenia fetida to their lethal and sublethal toxicity. Experiments were conducted in two soils with different organic matter contents to provide media with contrasting sorption capacity for the insecticides. The results showed that organophosphate CFVP was, when taken up by earthworms, rapidly and irreversibly bound to biomolecules and the fraction of extractable parent insecticide and metabolites was low. In contrast, alpha-CYP was rapidly metabolized by earthworms but did not form conjugates. It seems that the phase II metabolism of alpha-CYP is inhibited in earthworms, resulting in an increasing accumulation of its metabolites. Instantaneous binding of non-altered CFVP to the target site presumably resulted in a higher toxicity compared to alpha-CYP and explains the small difference between lethal and reproduction toxicity. For alpha-CYP, however, accumulation of alpha-CYP metabolites in earthworms during chronic exposure may explain the large observed difference between lethal and sublethal toxicity. Bioaccumulation and toxicity of either insecticide decreased with increasing organic matter content in soil, emphasizing the role of compound sorption on bioavailability and toxicity for soil organisms.

Chemical methods to assess bioavailability in soil and sediment often use synthetic polymers that mimic uptake of organic compounds in organisms or microbial degradation. In this paper we have assessed a biomimetic extraction method using hydroxyl-beta-cyclodextrin (HP-beta-CD) to estimate uptake of the two insecticides alpha-cypermethrin (alpha-CYP) and chlorfenvinphos (CFVP) in the earthworm Eisenia fetida. Additionally, a novel approach was developed to estimate the efficiency of biomimetic extractions. The study revealed that HP-beta-CD is a suitable surrogate for estimating the bioaccessibility of hydrophobic chemicals in soil. If one uses a 3.5 times higher amount of HP-beta-CD than soil, effective and reproducible extractions can be achieved within 48 h. Atthese conditions, inclusion of dissolved chemicals by HP-beta-CD mimics uptake of a given compound into earthworms and takes into account sorption-related aspects that control biological uptake. The data indicate that, with increasing hydrophobicity, the affinity of organic chemicals to HP-beta-CD does not increase to the same degree as to soil organic matter. Therefore, a high surplus of HP-beta-CD is necessaryto provide a sufficient extraction capacity in biomimetic extractions.

Alpha-cypermethrin, a synthetic pyrethroid, is used as an insecticide in agricultural settings and is increasingly replacing organophosphates and carbamates because of lower application rates and lower toxicity to mammals. Because very little is known about the acute and chronic toxicity of this compound for soil-living organisms, the present study investigated acute and sublethal toxicity of alpha-cypermethrin for four terrestrial invertebrate species in an agricultural soil from Norway. Bioassays with the earthworm Eisenia fetida, the potworm Enchytraeus crypticus, the springtail Folsomia candida, and the land snail Helix aspersa were performed according to slightly modified versions of Organization for Economic Cooperation and Development (Paris, France) or International Organization for Standardization (Geneva, Switzerland) guidelines and resulted in median lethal concentrations of greater than >1,000 to 31.4 mg/kg and sublethal no-observed-effect concentrations of 2.51 to 82 mg/kg. A high acute to chronic ratio was found, especially in the earthworms. Interspecies differences in sensitivity may be explained by differences in exposure and differences in metabolization rate. When based on measured pore-water concentrations, terrestrial species overall appear to be approximately one order of magnitude less sensitive than aquatic species. Effect assessments conducted according to European guideline for risk assessment of pesticides reveal that assessments based on acute toxicity tests are not always conservative enough to determine environmentally safe concentrations in soil. Mandatory incorporation of sublethal toxicity data will ensure that in regions with temperate climate, the effects of pesticides on populations of soil-living organisms are unlikely.

Despite the fact that creosote mainly consists of polycyclic aromatic hydrocarbons (PAHs), more polar compounds like phenolics, benzenes and N-, S-, O-heterocyclics dominate the groundwater downstream from creosote-contaminated sites. In this study, bioassay-directed fractionation, combined with fullscan GC-MS, identified organic toxicants in creosote-contaminated groundwater. An organic extract of creosote-contaminated groundwater was fractionated on a polar silica column using high performance liquid chromatography (HPLC), and the toxicity of the fractions was measured by the Microtox-bioassay. PAHs, which comprise up to 85% of pure creosote, accounted for only about 13% of total toxicity in the creosote-contaminated groundwater, while methylated benzenes, phenolics and N-heterocyclics accounted for ca. 80% of the measured toxicity. The fraction containing alkylated quinolines was the most toxic single fraction, accounting for 26% of the total measured toxicity. The results imply that focus on PAHs may underestimate risks associated with creosote-contaminated groundwater, and that environmental risk assessment should focus to a higher degree on substituted PAHs and phenolics because they are more toxic than the unsubstituted ones. Additionally, benzenes and N-heterocyclics (e.g., alkylated quinolines) should be assessed.

The International Standardization Organization recently launched a soil toxicity test with snails (Helix aspersa). We assessed the sensitivity of this test for seven polycyclic aromatic compounds. Control animals had 100% survival and low variability for growth measurements. Maximum exposure concentrations of 2800 mg/kg (4000 mg/kg for acridine) had no effect on survival. Similarly, growth (biomass and shell size) was not affected by pyrene, fluoranthene, fluorene, carbazole, phenanthrene, or acridine, whereas dibenzothiophene gave a 10% effect concentration of 1600 mg/kg. Measured internal concentrations of carbazole, dibenzothiophene, and acridine increased with increasing soil concentrations, but biota-soil accumulation factors were low (0.002-0.1). Compared to previously tested organisms, with all being exposed in the same soil type and under similar test conditions, the H. aspersa test was relatively insensitive to all substances.

Halogenated flame retardants have a high sorption affinity to particles, making soils and sediments important sinks. Here, three of the most commonly used flame retardants have been tested for sub-lethal toxicity towards soil nitrifying bacteria, a terrestrial plant (seed emergence and growth of the red clover, Trifolium pratense), and a soil invertebrate (survival and reproduction of Enchytraeus crypticus). Tetrabromobisphenol A (TBBPA) was quite toxic to enchytraeids, with significant effects on reproduction detected already at the 10 mgkg(-1) exposure level (EC(10)=2.7 mgkg(-1)). In contrast, decabromodiphenyl ether (DeBDE) was not toxic at all, and short-chain chloroparaffins (CP(10-13)) only affected soil nitrifying bacteria at the highest test concentration (EC(10)=570 mgkg(-1)). Exposure concentrations were verified by chemical analysis for TBBPA and DeBDE, but not for CP(10-13), as a reliable method was not available. Based on the generated data, a PNEC for soil organisms can be estimated at 0.3 mgkg(-1) for TBBPA and 57 mgkg(-1) for short-chain chloroparaffins. No PNEC could be estimated for DeBDE. Measurements of TBBPA in soil are not available, but measured concentrations in Swedish sludge are all lower than the estimated threshold value for biological effects in soil.

Benzotriazole is a commonly used additive in aircraft de-icing fluids. As a result of extensive de-icing activities the compound is detected in the groundwater below de-icing platforms at several international airports. The compound is toxic, and not biodegradable. Laboratory tests have been performed to study if UV irradiation can degrade the compound and reduce the aquatic toxicity. Benzotriazole can be degraded by UV irradiation at pH values below 7. Approximately 65% reduction in the benzotriazole concentration was achieved at a dose of 320 mWs/cm2, and almost 90% reduction was achieved at 1070 mWs/cm2, with an apparent first order relation between the logarithm to the UV dose and the reduction. Benzotriazole is not significantly mineralised by UV irradiation, but transformed into other compounds, of which aniline and phenazine were identified. The metabolites show toxic effects, but they are not as toxic as benzotriazole, resulting in a general decrease in toxicity as a result of UV irradiation.