Investigation of intermittent aeration and oxic settling anaerobic process combination for nitrogen removal and sewage sludge reduction.

A pilot plant with a conventional activated sludge (CAS) system with intermittent aeration (IA) was monitored. The system was configured as an Oxic Settling Anaerobic (OSA) process with the insertion of one anaerobic side-stream reactor (ASSR). The pilot plant was fed with real wastewater and an intensive experimental campaign was carried out including sludge minimization, nitrogen and carbon removal, GHG emissions and biokinetic parameters. The experimental campaign was divided into periods: Period I, II, and III. In Periods I and II, the ASSR reactor was operated with two different hydraulic retention times (HRT), 4 and 6 h, with an aeration/non-aeration ratio of 30 min/30 min. In Period III, the HRT in the anaerobic reactor was the same as in Period II. In contrast, the biological reactor's aerated/non-aerated ratio was increased to 40 min/20 min. Results demonstrated that combining IA and OSA might be effective in the reduction of excess sludge production. The yield coefficient decreased from Period I to Period II (Yobs from 0.41 to 0.25 gTSS gCOD-1, in Period I and II, respectively). Nevertheless, the HRT increase in the ASSR compromised the system performance regarding nitrification and greenhouse gas emissions and worsened the sludge settleability. However, the increase in the aeration duration was beneficial in restoring the system's nitrification and denitrification ability and carbon footprint. The lowest carbon footprint was obtained during Period III (6.8 kgCO2/d).

Tracing Gadolinium levels throughout wastewater treatment: Insights from a yearly assessment in northern Spain.

Gadolinium (Gd) is a rare earth element (REE) used in the formulation of contrast agents for Magnetic Resonance Imaging (MRI) due to its paramagnetic properties. The growth in population and the improved quality of the healthcare systems over the last years, has promoted the use of MRI as an effective diagnostic tool thus increasing the consumption of gadolinium and its release into the wastewater treatment network. Therefore, the tracking and quantification of this metal in sewage treatment plants and water bodies, is of paramount importance since there are currently no specific rare earth treatment technologies installed in WWTPs, and consequently gadolinium is finally discharged into the environment. In this work, the presence of gadolinium and all other rare earth elements was monitored during a year in three WWTPs in northern Spain (Vuelta Ostrera and San Román in Cantabria and Galindo in País Vasco). These WWTPs are located close to urban centres with hospitals where MRI tests are performed. By tracing Gd throughout the wastewater treatment facilities, its presence was confirmed in water streams, in the order of ng per litter, and in sludge and ashes, in the order of mg per kilogram. A significant human influence was observed, with Gd anomaly values between 3.14 and 79.2 and anthropogenic Gd percentages above 90 %. The presence of Gd in water streams is affected by the sampling period due to the variations of the activity periods of the hospitals nearby the treatment plants. On the contrary, its content in sludge and ashes remains almost constant along the year. The concentration of this metal found in the ashes opens the door to its possible recovery together with other critical raw materials in the context of the circular economy.

Adsorption enhanced biological treatment of hydrothermal liquefaction aqueous phase derived from municipal sludge.

Hydrothermal liquefaction (HTL) is a promising method for municipal sludge valorization through waste minimization and biofuel production. The process wastewater, HTL aqueous, presents a significant challenge for scale-up due to recalcitrant compounds. In this study, granular activated carbon (GAC) was used to remove potential inhibitors from HTL aqueous through adsorption to enhance aerobic and anaerobic biological treatment. GAC removed up to 61 % chemical oxygen demand (COD), 50 % biochemical oxygen demand (BOD) and potential inhibitors, such as total phenolic compounds (87 %) and N-heterocycles (90 % of pyridines) at 100 g/L. Conversely, most volatile fatty acids remained in HTL aqueous. Subsequently, mesophilic and thermophilic specific methane potential increased by up to 97 % and 83 %, respectively. BOD increased by up to 50 %, which enhanced BOD/COD ratio from 81 % to 93 % before and after adsorption. This study established the groundwork for HTL aqueous adsorption, described mechanism for pollutant removal, and provided insights for biological treatment.

Selective adsorption of antibiotics from human urine using biochar modified by dimethyl sulfoxide, deep eutectic solvent, and ionic liquid.

Antibiotics present in human urine pose significant challenges for the use of urine-based fertilizers in agriculture. This study introduces a novel two-stage approach utilizing distinct biochar types to mitigate this concern. Initially, a modified biochar selectively adsorbed azithromycin (AZ), ciprofloxacin (CPX), sulfamethoxazole (SMX), trimethoprim (TMP), and tetracycline (TC) from human urine. Subsequently, a separate pristine biochar was employed to capture nutrients. Biochar, derived from sewage sludge and pyrolyzed at 550 and 700°C, was modified using dimethyl sulfoxide, deep eutectic solvent, and ionic liquid to enhance antibiotic removal in the first stage. The modifications introduced hydrophilic functional groups (-OH/-COOH), which favor antibiotic adsorption. Adsorption kinetics followed the pseudo-second-order model, with the Langmuir isotherm model best describing the adsorption data. The maximum adsorption capacities for AZ, CPX, SMX, TMP, and TC after the modification were 196.08, 263.16, 81.30, 370.37, and 833.33 µg/g, respectively. Pristine biochar exhibited a superior ammonia adsorption capacity compared to the modified biochar. Hydrogen bonding, electrostatic attraction, and chemisorption drove antibiotic adsorption on the modified biochar. Regeneration efficiency declined due to solvent accumulation and potential byproduct formation on the biochar surface (<30% removal capacity after three cycles). This study presents innovative biochar modification strategies for selective antibiotic adsorption, laying the groundwork for environmentally friendly urine-based fertilizers in agriculture.

Investigation of thermal alkaline pretreatment of primary and waste activated sludge on the energy efficiency of sludge digestion.

Because of the naturally limited anaerobic degradability and limited biogas yield of raw sludge (RS), this study aims to increase the biogas production of primary sludge (PS) and waste activated sludge (WAS) by the integration of thermal alkaline process (TAP). PH 11 is confirmed to be the most suitable pH value for the TAP of both sludges. Moreover, with the pretreatment at pH 11 and 160 °C (6 bar) for 30 min, the investigated PSs and WASs achieved an increased biogas production of up to 81 % and 72 %, respectively. The improved net electricity production of WASs after TAP varied between 15-43 % compared to conventional WAS digestion. However, the TAP of PS at pH 11 enhanced the biogas production by 1-81 %, which did not constantly contribute to an improved net electricity production.

The effect of an acidic environment during the hydrothermal carbonization of sewage sludge on solid and liquid products: The fate of heavy metals, phosphorus and other compounds.

The pH of sewage sludge is a crucial factor during the hydrothermal carbonization process that influences the characteristics of the resulting products and migration of certain compounds from the solid to liquid phase. Accordingly, this work is focused on examining the pH impact during the HTC process, in particular, pH equals 2, 3, 4, 5 and 6 on the individual hydrothermally carbonized products generated at 200 °C and 2 h residence time. For this reason, the chemical and physical indicators describing the post-processing liquid and hydrochar were determined. For instance, it was observed that the phosphorus content detected in the liquid, derived at pH2, rose significantly by 80%. Furthermore, decreasing the pH of sewage sludge had a significant impact on the ash content and the calorific value of the hydrochar. Additionally, changes in the specific surface area of hydrochar were noticed: pH = 5 and pH = 6 showed an increase of 20-30%, while for lower pH values a decrease of c.a. 26% was achieved. The distribution of heavy metals between the obtained fractions in the HTC process (solid and liquid) indicated that 92 to almost 100% of the tested heavy metals were transferred to the hydrochar. A significant effect of pH on the distribution between these fractions was observed only for Zn and Ni. For instance, for pH = 2, Zn and Ni in post-processing liquid were 34% and 29%, respectively. In addition, the sequential extraction of heavy metals from hydrochar was also performed in order to identify mobile and non-mobile phases. It was noticed that the acidic environment favours a higher amount of mobile heavy metals in hydrochar. The largest effect was observed for Cd, Pb, Cr and Cu, for which, at pH = 2, their respective amounts in the mobile fraction were 2.7; 3.6; 1.8; 6.2 times higher, compared to the hydrochar without pH correction.

Biodiesel production from sewage sludge using supported heteropolyacid as heterogeneous acid catalyst.

Phosphotungstic acid (HPW) and silicotungstic acid (HSiW) were tested as homogeneous and as heterogeneous catalysts (after immobilized on different supports as high surface area graphite -HSAG500-, montmorillonite -MMT- and alumina -Al2O3-) for the in situ transesterification of sewage sludge lipids. Both catalysts exhibited similar performance in homogeneous phase, with slightly higher biodiesel yield for HPW. When the different supports were tested with HPW, the maximum yield obtained follow the trend: MMT > HSAG500 > Al2O3, but a greater leaching of the heteropolyacid (HPA) was observed with MMT. Therefore, HSAG500 showed the best results with a good FAMEs profile. The percentage of active phase was optimized from 1 to 40%, reaching the optimum at 10%. A more heterogeneous surface is obtained with larger quantities, also favouring the HPA leaching. The reaction temperature and the use of sonication as pre-treatment were also optimized. The best results were obtained after sonication with HPW-HSAG500 (10%) as catalyst, catalyst/sludge ratio 1:2, MeOH/sludge ratio 33:1, 120 °C and 21 h of reaction time with a maximum biodiesel yield of 31.1 % (FAMEs/lipids). In view of the results obtained HPW supports on HSAG500 offers a novel alternative as heterogeneous acid catalyst for in situ transesterification using sewage sludge as raw material.

Guidelines for efficient nitrogen preservation in sewage sludge-based fertilizers.

This study explores sustainable methods to mitigate nitrogen (N) loss in agriculture amid rising food demands and limited arable land. It examines sewage sludge (SS) as an alternative to synthetic N fertilizers. SS is rich in nitrogen (4.21 ± 0.42 %) and phosphorus (3.60 ± 0.72 %), making it suitable for nutrient recovery and soil enhancement. Unfavorable sludge management methods result in the loss of 950,000 tons of nitrogen, meeting almost 10 % of the EU's nitrogen fertilization demand. This research evaluates SS treatment methods, including chemical conversion, thermal treatment, and biological composting, focusing on nitrogen conservation efficiency. Results show nitrogen loss during hydrolysis is minimized at pH 4 to 8 but increases significantly as ammonia (NH3) at pH 9 to 11, ranging from 4.2 % to 9 %. Neutralizing the hydrolysate is crucial; using solid KOH resulted in 13.5 % nitrogen loss, 11 times more than using slightly alkaline ash (1.22 %). Adding ash during drying reduced nitrogen emissions by 30 % compared to traditional drying at 105 °C. Improving the C/N ratio with food residues reduced nitrogen losses by 46.3 % during composting. These findings highlight the importance of pH control in chemical processes and temperature regulation in thermal treatments. Adding residues from other processes, such as biomass combustion waste, enhances SS processing conditions. Understanding nitrogen retention mechanisms is crucial for the environmental sustainability of SS usage. Efficient nitrogen retention strategies improve the fertilization value of SS and reduce its environmental footprint by lowering greenhouse gas emissions, particularly ammonia. Reducing nitrogen loss during SS treatment significantly lowers ammonia emissions, a major contributor to greenhouse gas emissions. These results help determine optimal methods for managing and processing SS to minimize emissions and increase agricultural usability.

Combined effect of thermal hydrolysis process and low-temperature pyrolysis on the classification and bioavailability of phosphorus in sewage sludge.

Existing phosphorus (P) resources are becoming increasingly scarce, so it is necessary to recover P from potential sources. This paper is based on thermal hydrolysis process (THP) at 140-180 °C, coupled with low-temperature pyrolysis at 300 °C, to study its effect on the recovery and conversion of P from sewage sludge. Most significant change was observed in apatite P, which increased from 3.43 ± 0.48 mg/g in raw sludge to 30.17 ± 1.17 mg/g in biochar (BTHP-180-4-300) during optimal process (THP condition: 180 °C, 4 h; pyrolysis condition: 300 °C). Reactions between phosphates and metal ions became more complete during this combined process. Unstable forms of P were converted into more stable forms, with transformations from Al-P and Fe-P toward Ca-P compounds like Ca3(PO4)2, Ca3Mg3(PO4)4, Ca2P2O7, and Ca(H2PO4)2, making P less degradable and more suitable as slow-release fertilizers. Additionally, P characteristics of actual THP in a sewage treatment plant were similar to those of laboratory THP.

Enzymatic hydrolysis of waste streams originating from wastewater treatment plants.

BACKGROUND: Achieving climate neutrality is a goal that calls for action in all sectors. The requirements for improving waste management and reducing carbon emissions from the energy sector present an opportunity for wastewater treatment plants (WWTPs) to introduce sustainable waste treatment practices. A common biotechnological approach for waste valorization is the production of sugars from lignocellulosic waste biomass via biological hydrolysis. WWTPs produce waste streams such as sewage sludge and screenings which have not yet been fully explored as feedstocks for sugar production yet are promising because of their carbohydrate content and the lack of lignin structures. This study aims to explore the enzymatic hydrolysis of various waste streams originating from WWTPs by using a laboratory-made and a commercial cellulolytic enzyme cocktail for the production of sugars. Additionally, the impact of lipid and protein recovery from sewage sludge prior to the hydrolysis was assessed. RESULTS: Treatment with a laboratory-made enzyme cocktail produced by Irpex lacteus (IL) produced 31.2 mg sugar per g dry wastewater screenings. A commercial enzyme formulation released 101 mg sugar per g dry screenings, corresponding to 90% degree of saccharification. There was an increase in sugar levels for all sewage substrates during the hydrolysis with IL enzyme. Lipid and protein recovery from primary and secondary sludge prior to the hydrolysis with IL enzyme was not advantageous in terms of sugar production. CONCLUSIONS: The laboratory-made fungal IL enzyme showed its versatility and possible application beyond the typical lignocellulosic biomass. Wastewater screenings are well suited for valorization through sugar production by enzymatic hydrolysis. Saccharification of screenings represents a viable strategy to divert this waste stream from landfill and achieve the waste treatment and renewable energy targets set by the European Union. The investigation of lipid and protein recovery from sewage sludge showed the challenges of integrating resource recovery and saccharification processes.

Sustainable Valorisation of Sewage Sludge via Carbon Dioxide-Assisted Pyrolysis.

The escalating volume of sewage sludge (SS) generated poses challenges in disposal, given its potential harm to the environment and human health. This study explored sustainable solutions for SS management with a focus on energy recovery. Employing CO2-assisted pyrolysis, we converted SS into flammable gases (H2 and CO; syngas). Single-stage pyrolysis of SS in a CO2 conditions demonstrated that CO2 enhances flammable gas production (especially CO) through gas phase reactions (GPRs) with volatile matter (VM) at temperatures ≥ 520 ˚C. Specifically, the CO2 partially oxidized the VM released from SS and concurrently underwent reduction into CO. To enhance the syngas production at temperatures ≤ 520 ˚C, multi-stage pyrolysis setup with additional heat energy and a Ni/Al2O3 catalyst were utilized. These configurations significantly increased flammable gas production, particularly CO, at temperatures ≤ 520 ˚C. Indeed, the flammable gas yield in the catalytic pyrolysis of SS increased from 200.3 mmol under N2 conditions to 219.2 mmol under CO2 conditions, representing a 4.4-fold increase compared to single-stage pyrolysis under CO2 conditions (50.0 mmol). By integrating a water-gas-shift reaction, the flammable gases produced from CO2-assisted catalytic pyrolysis were expected to have the potential to generate revenue of US$4.04 billion. These findings highlight the effectiveness of employing CO2 in SS pyrolysis as a sustainable and effective approach for treating and valorising SS into valuable energy resources.

Novel strategy for efficient energy recovery and pollutant control from sewage sludge and food waste treatment.

Considering the high organic matter contents and pollutants in sewage sludge (SS) and food waste (FW), seeking green and effective technology for energy recovery and pollutant control is a big challenge. In this study, we proposed a integrated technology combing SS mass separation by hydrothermal pretreatment, methane production from co-digestion of hydrothermally treated sewage sludge (HSS) centrate and FW, and biochar production from co-pyrolysis of HSS cake and digestate with heavy metal immobilization for synergistic utilization of SS and FW. The results showed that the co-digestion of HSS centrate with FW reduced the NH4+-N concentration and promoted volatile fatty acids conversion, leading to a more robust anaerobic system for better methane generation. Among the co-pyrolysis of HSS cake and digestate, digestate addition improved biochar quality with heavy metals immobilization and toxicity reduction. Following the lab-scale investigation, the pilot-scale verification was successfully performed (except the co-digestion process). The mass and energy balance revealed that the produced methane could supply the whole energy consumption of the integrated system with 26.2 t biochar generation for treating 300 t SS and 120 t FW. This study presents a new strategy and technology validation for synergistic treatment of SS and FW with resource recovery and pollutants control.

Sewage sludge pyrolysis 'kills two birds with one stone': Biochar synergies with persulfate for pollutants removal and energy recovery.

The disposal and resource utilization of sewage sludge (SS) have always been significant challenges for environmental protection. This study employed straightforward pyrolysis to prepare iron-containing sludge biochar (SBC) used as a catalyst and to recover bio-oil used as fuel energy. The results indicated that SBC-700 could effectively activate persulfate (PS) to remove 97.2% of 2,4-dichlorophenol (2,4-DCP) within 60 min. Benefiting from the appropriate iron content, oxygen-containing functional groups and defective structures provide abundant active sites. Meanwhile, SBC-700 exhibits good stability and reusability in cyclic tests and can be easily recovered by magnetic separation. The role of non-radicals is emphasized in the SBC-700/PS system, and in particular, single linear oxygen (1O2) is proposed to be the dominant reactive oxygen. The bio-oil, a byproduct of pyrolysis, exhibits a higher heating value (HHV) of about 30 MJ/kg, with H/C and O/C ratios comparable to those of biodiesel. The energy recovery rate of the SS pyrolysis system was calculated at 80.5% with a lower input cost. In conclusion, this investigation offers a low-energy consumption and sustainable strategy for the resource utilization of SS while simultaneously degrading contaminants.

Extracellular-proton-transfer driving high energy-conserving methanogenesis in anaerobic digestion.

Anaerobic digestion (AD) is a promising technology to realize the conversion from organic matters to methane, which is highly mediated by syntrophic microbial community via mutualistic interactions. However, small energy available in methanogenic conversion usually limits the metabolic activity. To adapt such energy-limited environment, efficient energy conservation is critical to support active physiological functions of anaerobic consortia for methanogenic metabolism. In this study, the contribution of extracellular proton transfer (EPT) enhancement to achieving energy-conserving methanogenesis in AD was explored. Proton-conductive medium (PCM) was applied to construct efficient proton transport pathway, and a large number of protons from extracellular water were found available to upregulate methanogenesis in AD, as indicated by the increase in the content of 2H (D) in methane molecules (over 40.7%), among which CO2-reduction-to-CH4 was effectively enhanced. The increases of adenosine triphosphate (ATP) concentration (+54.1%) and gene expression activities related to ATPase (+100.0%) and proton pump (+580.1%) revealed that enhanced EPT by PCM promoted transmembrane proton motive force generation to facilitate ATP synthesis. Based on genome-centric metatranscriptomic analyses, MAG14, MAG63 and MAG61 with high energy conservation activity displayed most pronounced positive response to the EPT enhancement. In these core MAGs, the metabolic pathway reconstruction and the key genes activity identification further proved that EPT enhancement-driven efficient ATP synthesis stimulated the cross-feeding of carbon and proton/electron to facilitate microbial mutualism, thereby resulting in the high energy-conserving methanogenesis. Overall, our work provides new insights into how EPT enhancement drives high energy-conserving methanogenesis, expanding our understanding of the ecological role of EPT in AD.

Characteristics of nutrients and heavy metals release from sewage sludge biochar produced by industrial-scale pyrolysis in the aquatic environment and its potential as a slow-release fertilizer and adsorbent.

To assess the application potential of sewage sludge biochar produced by industrial-scale pyrolysis (ISB), the release characteristics of nutrients (NH4+, PO43-, K, Ca, Mg and Fe) and heavy metals (Mn, Cu, Zn, Pb, Ni and Cr) were investigated. Their release amounts increased with decreasing initial pH and increasing solid-liquid ratios (RS-L) and temperature. The release types of NH4+, K, Mg, and Mn were diffusion/dissolution, while those of Cu, Zn, Pb, Ni, and Cr were diffusion/resorption. The release types of PO43- and Ca varied with initial pH and RS-L, respectively. The chemical actions played dominant roles in their release, while particle surface diffusion and liquid film diffusion determined the rates of diffusion and resorption phases, respectively. The release of NH4+, PO43-, K, Ca, Mg, Mn and Zn was a non-interfering, spontaneous (except PO43-), endothermic, and elevated randomness process. The release efficiency of NH4+, PO43- and K met the Chinese standard for slow-release fertilizers, while the total risk of ISB was low. The eutrophication and potential ecological risks of ISB were acceptable when the dose was less than 3 g L-1 and the initial pH was no lower than 3. In conclusion, ISB had potential as a slow-release fertilizer and adsorbent.

Carbide slag and sodium metasilicate synergistic activation of sludge ash-based alkali-activated materials: Towards a cleaner activation approach.

Traditional activators such as sodium hydroxide and sodium silicate are commonly used in the preparation of alkali-activated materials; however, their significant environmental impact, high cost, and operational risks limit their sustainable use in treating solid waste. This study explores the innovative use of carbide slag (CS) and sodium metasilicate (NS) as alternative activators in the production of sewage sludge ash-based alkali-activated materials (SSAM) with the aim of reducing the carbon footprint of the preparation process. The results demonstrate that CS effectively activates the sewage sludge ash, enhancing the compressive strength of the SSAM to 40 MPa after curing for 28 d. When used in conjunction with NS, it synergistically improves the mechanical properties. Furthermore, the microstructure and phase composition of the SSAM are characterized. Increasing the quantities of CS and NS accelerates the dissolution of the precursor materials, promoting the formation of a higher quantity of hydration products. This significantly reduces the number of voids and defects within the samples, further enhancing the densification of the microstructure. Environmental assessments reveal that CS and NS offer substantial sustainability benefits, confirming the feasibility of activating SSAM using these materials. This approach provides a less energy-intensive and more environmentally friendly alternative to conventional activation methods and presents an effective strategy for managing large volumes of sewage sludge ash and CS.

Direct air capture of CO2 using biochar prepared from sewage sludge: Adsorption capacity and kinetics.

As an emerging carbon-negative emission technology, carbon dioxide (CO2) capture from the air is an essential safeguard for alleviating global warming. Sludge-activated carbon with excellent mesoporous structure is a potential material for CO2 capture. In this paper, the amino modified sewage sludge materials were used to prepare the porous CO2 adsorbent from air. The effect of preparation conditions on the microstructure of sewage sludge-based activated carbon materials was analyzed by microstructural characterization, and the impacts of activator, pyrolysis temperature, and the concentration of modifier on the CO2 adsorption performance of sewage sludge-based activated carbon materials were also systematically investigated. The results show that the pyrolysis temperature, the type of activator and the modifier concentration significantly affect the adsorption performance of sewage sludge-based CO2 adsorption materials. Among them, the sewage sludge-based CO2 adsorption material prepared with solid NaOH as an activator, with an activation temperature of 600 °C and loading concentration of 20 %, exhibited the best performance, that is the CO2 adsorption capacity reached 1.17 mmol/g, and the half time is about four min, which shows better performance, compared with other adsorbents for CO2 capture from air. The research results can reduce CO2 emissions on the one hand, and on the other hand, realize the resourceful utilization of sewage sludge, which sheds light on "treating the wastes with wastes".

Plant litter as a heavy metal migration strategy following application of sewage sludge to subtropical forest soils.

The environmental risks of migration of heavy metals (HMs) following applications of sewage sludge (SS) to forest soils are garnering increased attention. Plant litter at the forest floor may modify HM migration pathways through impacts on soil aggregates and water/soil erosion; however, HM migration responses to plant litter are poorly understood. The aim of this study was to determine the effects of plant litter cover on HMs migration, and water and soil erosion following the application of SS to subtropical forest soils. Effects of addition of SS along and SS plus plant litter at 0.75 or 1.5 kg m-2 on the migration of cadmium, chromium, copper, nickel, lead, and zinc in surface runoff, soil interflow, and sediments were quantified across nine simulated rainfall events in a laboratory experiment and following natural intense rain events in a field experiment. Addition of SS elevated HM concentrations in surface runoff by 38.7 to 98.5 %, in soil interflow by 48.3 to 312.5 %, and in sediment by 28.5 to 149.4 %, and increased the production of sediment aggregates <0.05 mm that led to greater cumulative migrations of HMs in surface runoff and sediment; sediment accounted for 89.5 % of HM migrations. Addition of plant litter reduced cumulative migration of HMs by 87.1-97.27 %; however, the higher rate of plant litter led to a decrease in surface runoff and sediment yield, and an increase in soil interflow. Addition of plant litter shifted the main pathway of HM migration from sediment to surface runoff and soil interflow. The potential ecological HM risk index was "low" for each treatment. We found consistency in HM concentrations and migrations via surface runoff between the field and laboratory experiments. Overall, the addition of plant litter with SS mitigated soil erosion and reduced total migration of HMs, resulting in a 88.7-97.3 % decrease in the ecological risk index of the six HMs. We conclude that the addition of plant litter may provide a management strategy for the mitigation of HM risks to environmental safety for the disposal of SS in subtropical forest systems.

Hazards of toxic metal(loid)s: Exploring the ecological and health risk in soil-crops systems with long-term sewage sludge application.

Sewage sludge (SS) is commonly used as agricultural fertilizer worldwide. However, the toxic metal(loid)s in SS raises concerns about soil contamination and the potential risks to human health. This study, conducted since 2007 on the North China Plain, examines the impact of SS use on crops. An experiment was designed with five treatments: conventional fertilization (CK) and four levels of SS application (W1, W2, W3, and W4: 4.5, 9.0, 18.0, and 36.0 t ha-1, respectively). Soil concentrations of eight toxic metal(loid)s (Zn, Cu, Cr, Cd, Ni, Pb, As, and Hg) were analyzed to assess pollution risk using various indices. Health risks associated with maize and wheat grains were also evaluated. Additionally, the impact of long-term SS application on crop yield, soil quality, and human health within a wheat-maize rotation system was examined. SS application increased wheat and maize yields by 5.37 to 19.08 % and 6.97 to 17.94 %, respectively, across treatments W2 to W4. Despite the toxic metal(loid)s in the grains remaining within safe limits, their concentrations showed an upward trend, especially under the W4 treatment. Moreover, SS application significantly increased the soil Zn, Cu, Cr, Cd, Pb, and Hg levels (P < 0.05) without exceeding the national standards. The geo-accumulation index values revealed rising pollution levels for Zn, Cu, Cd, and Hg, which shifted from no contamination to moderate contamination and then to moderate-to-high contamination, yet the overall pollution level remained safe. Soil ecological risks increased from moderate to serious, with Hg posing the greatest risk, particularly under the W4 treatment. Long-term crop intake from the area significantly exposed children and adults to As, contributing 42.12 % and 34.62 % to hazard index (HI), respectively. The HI values for toxic metal(loid)s in these grains surpassed one in both age groups, suggesting health risks from long-term SS cultivated crops.

Effect of polyethylene terephthalate plastics on nitrogen, sulphur and chlorine contaminants via sludge pyrolysis and Pb/Cu adsorption properties of biochar.

Pyrolysis is an effective process for disposing of municipal sewage sludge (SS). Plastics can affect the SS pyrolysis behaviour and pyrolysis products due to their low ash and high hydrocarbon ratio. The secondary pollutants from the pyrolysis process may also be affected. Therefore, polyethylene terephthalate (PET), a typical plastic, was chosen to investigate the release characteristics of pollutants containing nitrogen, sulphur, and chlorine via SS pyrolysis, and the changes of biochar to adsorb two typical heavy metals, Pb and Cu. The pyrolysis of PET plastics facilitates the migration of N toward solid and liquid-phase products, S and Cl to the gas-phase products via pyrolysis. Oxygenated compounds of pyrolytic volatiles decreased from 38.18% to 28.43%, concurrently promoting the formation of phenolic compounds. The co-pyrolysis improved the quality of biochar and the ability to adsorb Pb and Cu. This systematic study can provide some support for the further improvement of SS pyrolysis technology, and will also be beneficial for subsequent applications.