Changes in organic matter composition during composting of two digested sewage sludges

Changes in the chemical and chemical-structural composition of the organic matter of two different sewage sludges (aerobic and anaerobic) mixed with sawdust (1:1 and 1:3, v/v) during composting were determined by monitoring chemical and microbiological parameters as well as by pyrolysis-gas chromatography. Composting was carried out in periodically turned outdoor piles, which were sampled for analysis 1, 30, 60 and 90 days after the beginning of the composting process. Both volatile organic matter and the water soluble C fraction decreased during composting, indicating that the more labile C fractions are mineralized during the process. Microbial activity as measured by microbial respiration (CO(2) evolved from compost samples during incubation) also decreased with composting, reflecting the more stable character of the resulting compost. No major differences were observed between the four composts studied as regards their chemical-structural characteristics. The acetonitrile, acetic acid and phenol pyrolytic fragment tended to increase with composting. Although the final composts were more aromatic in nature than the starting materials, a low degree of humification was observed in all four composts studied, as determined by their high proportion of polysaccharides and alkyl compounds. For this reason, the relationship between pyrolytic fragments, such as benzene/toluene or benzene+toluene/pyrrol+phenols, which are used as indices of humification for soil organic matter, are not of use for such poorly evolved sludge composts; instead, ratios that involve carbohydrate derivatives and aromatic compounds, such as furfural+acetic/benzene+toluene or acetic/toluene, are more sensitive indices for reflecting the transformations of these materials during composting. Both the chemical and microbiological parameters and pyrolytic analysis provided valuable information concerning the nature of the compost's organic matter and its changes during the composting process.     

Changes in soil chemical and microbiological properties during 4 years of application of various organic residues

A 4-year field trial was established in eastern Sweden to evaluate the effects of organic waste on soil chemical and microbiological variables. A simple crop rotation with barley and oats was treated with either compost from household waste, biogas residue from household waste, anaerobically treated sewage sludge, pig manure, cow manure or mineral fertilizer. All fertilizers were amended in rates corresponding to 100kgNha(-1)year(-1). The effects of the different types of organic waste were evaluated by subjecting soil samples, taken each autumn 4 weeks after harvest, to an extensive set of soil chemical (pH, Org-C, Tot-N, Tot-P, Tot-S, P-AL, P-Olsen, K-AL, and some metals) and microbiological (B-resp, SIR, microSIR active and dormant microorganisms, PDA, microPDA, PAO, Alk-P and N-min) analyses. Results show that compost increased pH, and that compost as well as sewage sludge increased plant available phosphorus; however, the chemical analysis showed few clear trends over the 4 years and few clear relations to plant yield or soil quality. Biogas residues increased substrate induced respiration (SIR) and, compared to the untreated control amendment of biogas residues as well as compost, led to a higher proportion of active microorganisms. In addition, biogas residues increased potential ammonia oxidation rate (PAO), nitrogen mineralization capacity (N-min) as well as the specific growth rate constant of denitrifiers (microPDA). Despite rather large concentrations of heavy metals in some of the waste products, no negative effects could be seen on either chemical or microbiological soil properties. Changes in soil microbial properties appeared to occur more rapidly than most chemical properties. This suggests that soil microbial processes can function as more sensitive indicators of short-term changes in soil properties due to amendment of organic wastes.     

Bioremediation of contaminated soil and sediment by composting

There are many well‐established bioremediation technologies applied commercially at contaminated sites. One such technology is the use of compost material. Composting matrices and composts are rich sources of microorganisms, which can degrade contaminants to innocuous compounds such as carbon dioxide and water. In this article, composting of contaminated soil and sediment was performed on a laboratory bench‐scale pile. Fertilizer was added to increase the nutrient content, and the addition of commercial compost provided a rich source of microorganisms. After maintaining proper composting conditions, the feasibility of composting was assessed by monitoring pH, total volatile solids, total microbial count, temperature, and organic contaminant concentration. The entire composting process occurred over a period of five weeks and resulted in the degradation of contaminants and production of compost with a high nutritional content that could be further used as inocula for the treatment of hazardous waste sites. © 2006 Wiley Periodicals, Inc.     

Heavy metals fractionation before, during and after composting of sewage sludge with natural zeolite

The main limiting factor, in order to use compost in agriculture, is the total concentration of heavy metals. Natural zeolites, such as clinoptilolite, have the ability to take up and remove those metals by utilizing ion exchange. However, it is important to know about the fractionation of the heavy metals during the thermophilic phase and the maturation phase. The purpose of this work was to determine the changes in the fraction of heavy metals in sewage sludge compost in which clinoptilolite is used as a bulking agent to remove metals. The final result indicates that a significant (p < 0.05) percentage of the metals, which is not removed by the zeolite, is associated with the residual fraction which is considered as an inert form.     

Changes in soil characteristics during landfill leachate irrigation of Populus deltoides

The effects of wastewater application on electrical conductivity, water retention and water repellency of soils planted with Populus deltoides (eastern cottonwood) and irrigated with different concentrations of landfill leachate and compost wastewater, tap water and nutrient solution were evaluated. Substrate water content at field capacity (?0.033 MPa) and at permanent wilting point (?1.5 MPa) was determined with a pressure plate extractor to assess available water capacity of the substrate. A water drop penetration test was used to determine substrate water repellency. The biomass of nutrient and landfill leachate treatments was significantly (P < 0.05) greater compared to the tap water and compost wastewater treatments. All treatments increased substrate water content at field capacity and at permanent wilting point. Landfill leachate significantly increased available water capacity (up to 52%); treatment with compost wastewater significantly decreased it (25–47%). All substrates showed increased water repellency after the experiment at field capacity and permanent wilting point comparing to the original substrate. The strongest influence on water repellency at both field capacity and permanent wilting point showed irrigation with compost wastewater and tap water. Pronounced influence on substrate’s water repellency of compost wastewater could be contributed to a high content of dissolved organic carbon, whereas Mg and Ca cations caused flocculation and consequent water repellency of the substrate irrigated with tap water. The results indicate that soil physical characteristics must be closely monitored when landfill leachate and compost wastewater are used for irrigation to avoid long term detrimental effects on the soil, and consequently on the environment. Due to the complexity of the compost wastewater quality the latter should be applied on open fields only after prior pre-treatment to reduce dissolved organic carbons, or alternatively, compost wastewater should be added only intermittently and in diluted ratios.     

Changes in the chemical and physicochemical properties of the solid fraction of cattle slurry during composting using different aeration strategies

Replacement of peat as a growing medium by a renewable material, such as an organic waste, is an issue of concern since harvesting of peat has a considerable environmental impact and, actually, it is a non-renewable resource. Cattle manure is a readily available organic waste, which means that once it goes through the composting process, it can be used as an alternative to peat, specifically, the solid fraction obtained from mechanical liquid-solid separation of cattle slurry (SF). Studies have shown it to be suitable for such uses. The purpose of this study was to detect possible changes in the physicochemical and chemical properties of SF when it is composted using different aeration strategies, with an emphasis on the changes that would make it feasible for use as a substrate. With this aim in mind, an experiment was designed with three aeration strategies that would be used during composting. The first consisted of applying air through a static method (forced ventilation). The second involved improving aeration by adding a bulking agent and a dynamic turning method. In the third strategy, aeration was carried out by turning (control). The results show that the different aeration strategies had a clear effect on the evolution of pH, electrical conductivity (EC), nitrate-N, ammonia-N and bicarbonate content. Nitrification was favored under good aeration conditions using the static composting method, probably due to the greater availability of ammonia-N that was transformed into nitrate-N. In general, the low buffering capacity allowed for a reduction of the pH during the curing stage of composting (in conjunction with low temperatures during this period), a characteristic that favors the use of this compost as a growing medium. We also conclude that measuring bicarbonate levels during composting could be used as an indicator of the possible acidification of the material and as a way of evaluating the level of material aeration.     

Decline in extractable antibiotics in manure-based composts during composting

A wide variety of antibiotics have been detected in natural water samples and this is of potential concern because of the adverse environmental effects of such antibiotic residues. One of the main sources of antibiotics effluence to the surrounding environment is livestock manures which often contain elevated concentrations of veterinary antibiotics (VAs) which survive digestion in the animal stomach following application in animal husbandry practices. In Korea, livestock manures are normally used for compost production indicating that there is potential for antibiotic release to the environment through compost application to agricultural lands. Therefore, reduction of the amount of VAs in composts is crucial. The purpose of this study was to understand the influence of the composting process and the components of the compost on the levels of three common classes of antibiotics (tetracyclines, sulfonamides, and macrolides). Composted materials at different stages of composting were collected from compost manufacturing plants and the variation in antibiotic concentrations was determined. Three different antibiotics, chlortetracycline (CTC), sulfamethazine (SMZ), and tylosin (TYL) at three different concentrations (2, 10, and 20 mg kg⁻¹) were also applied to a mixture of pig manure and sawdust and the mixtures incubated using a laboratory scale composting apparatus to monitor the changes in antibiotic concentrations during composting together with the physicochemical properties of the composts. During composting, in both field and lab-scale investigations, the concentrations of all three different antibiotics declined below the relevant Korean guideline values (0.8 mg kg⁻¹ for tetracyclines, 0.2 mg kg⁻¹ for sulfonamides and 1.0 mg kg⁻¹ for macrolides). The decline of tetracycline and sulfonamide concentrations was highly dependent on the presence of sawdust while there was no influence of sawdust on TYL decline.     

Depletion of chlortetracycline during composting of aged and spiked manures

Chlortetracycline (CTC) is one of the most important pharmaceuticals occurring in the environment. An increase of its application as feed supplement for livestock and poultry in the world leads to a substantial CTC contamination of manures, because most of the CTC is excreted to manure. The simulation experiment of aerobic composting was adopted to investigate CTC depletion in aged and spiked manure composting, and to address the extent of CTC depletion during composting. The results showed that the extractable CTC initial concentration was markedly different between the different manures, with 94.71mgkg(-1) in broiler manure and 879.6mgkg(-1) in hog manure. The concentration of extractable CTC decreased rapidly at the initial stage of composting, and subsequently declined slowly during aged and spiked manure composting. At the end of composting, more than 90% of CTC in the manure composting process (42 days) was depleted, except for hog manure composting with a removal of only 27%. The CTC half-lives were 11.0 days in broiler manure, 86.6 days in hog manure, 12.2 days in layer-hen manure (150.3mgkg(-1) CTC), 12.0 days in layer-hen manure (100.0mgkg(-1) CTC) and 4.39 days in layer-hen manure (53.10mgkg(-1) CTC), all according to the first order kinetics. The significance of experimental parameters in CTC depletion was assessed by the Pearson correlation approach. Microbial degradation of CTC was not effective from manure composting. CTC depletion was in good correlation with total organic carbon, total nitrogen, total phosphorus, C/N, N/P and total heavy metals.     

Utilization of solar energy in sewage sludge composting: Fertilizer effect and application

Three reactors, ordinary, greenhouse, and solar, were constructed and tested to compare their impacts on the composting of municipal sewage sludge. Greenhouse and solar reactors were designed to evaluate the use of solar energy in sludge composting, including their effects on temperature and compost quality. After 40 days of composting, it was found that the solar reactor could provide more stable heat for the composting process. The average temperature of the solar reactor was higher than that of the other two systems, and only the solar reactor could maintain the temperature above 55 °C for more than 3 days. Composting with the solar reactor resulted in 31.3% decrease in the total organic carbon, increased the germination index to 91%, decreased the total nitrogen loss, and produced a good effect on pot experiments.     

Chromium in soil layers and plants on closed landfill site after landfill leachate application

Landfill leachate (LL) usually contains low concentrations of heavy metals due to the anaerobic conditions in the methanogenic landfill body after degradation of easily degradable organic matter and the neutral pH of LL, which prevents mobilization and leaching of metals. Low average concentrations of metals were also confirmed in our extensive study on the rehabilitation of an old landfill site with vegetative landfill cover and LL recirculation after its treatment in constructed wetland. The only exception was chromium (Cr). Its concentrations in LL ranged between 0.10 and 2.75 mg/L, and were higher than the concentrations usually found in the literature. The objectives of the study were: (1) to understand why Cr is high in LL and (2) to understand the fate and transport of Cr in soil and vegetation of landfill cover due to known Cr toxicity to plants. The total concentration of Cr in LL, total and exchangeable concentrations of Cr in landfill soil cover and Cr content in the plant material were extensively monitored from May 2004 to September 2006. By obtained data on Cr concentration in different landfill constituents, supported with the data on the amount of loaded leachate, amount of precipitation and potential evapotranspiration (ETP) during the performance of the research, a detailed picture of time distribution and co-dependency of Cr is provided in this research. A highly positive correlation was found between concentrations of Cr and dissolved organic carbon (r = 0.875) in LL, which indicates the co-transport of Cr and dissolved organic carbon through the system. Monitoring results showed that the substrate used in the experiment did not contribute to Cr accumulation in the landfill soil cover, resulting in percolation of a high proportion of Cr back into the waste layers and its circulation in the system. No negative effects on plant growth appeared during the monitoring period. Due to low uptake of Cr by plants (0.10–0.15 mg/kg in leaves and 0.05–0.07 mg/kg in stems of Salix purpurea), the estimated Cr offtake from LL by plants represented only a small proportion of the LL Cr mass load during the observation period, resulting in no dispersion of Cr into the environment through leaf drop.     

Dynamic of functional microbial groups during mesophilic composting of agro-industrial wastes and free-living (N2)-fixing bacteria application

Although several reports are available concerning the composition and dynamics of the microflora during the composting of municipal solid wastes, little is known about the microbial diversity during the composting of agro-industrial refuse. For this reason, the first parts of this study included the quantification of microbial generic groups and of the main functional groups of C and N cycle during composting of agro-industrial refuse. After a generalized decrease observed during the initial phases, a new bacterial growth was observed in the final phase of the process. Ammonifiers and (N₂)-fixing aerobic groups predominated outside of the piles whereas, nitrate-reducing group increased inside the piles during the first 23 days of composting. Ammonia-oxidizing bacteria (AOB) and nitrite-oxidizing bacteria (NOB), showed an opposite trend of growth since ammonia oxidation decreased with the increase of the nitrite oxidation activity. Pectinolytics, amylolytics and aerobic cellulolytic were present in greater quantities and showed an upward trend in both the internal and external part of the heaps.Several free-living (N₂)-fixing bacteria were molecularly identify as belonging especially to uncommon genera of nitrogen-fixing bacteria as Stenotrophomonas, Xanthomonas, Pseudomonas, Klebsiella, Alcaligenes, Achromobacter and Caulobacter. They were investigated for their ability to fix atmospheric nitrogen to employ as improvers of quality of compost. Some strains of Azotobacter chrococcum and Azotobacter salinestris were also tested. When different diazotrophic bacterial species were added in compost, the increase of total N ranged from 16% to 27% depending on the selected microbial strain being used. Such microorganisms may be used alone or in mixtures to provide an allocation of plant growth promoting rhizobacteria in soil.     

Analysis of bacterial activity, biomass and diversity during windrow composting

Two contrasting compost windrows were monitored for various physical, chemical and microbiological parameters for a period of 106 days. The different input materials and management practises gave rise to different temperature, moisture, and oxygen consumption profiles as composting proceeded. However, despite the different composting conditions, the specific respiratory activity, as determined by oxygen consumption per bacterial cell, was remarkably similar for both windrows. Further investigations into diversity dynamics were done through DGGE and cloning and sequencing of bacterial 16S rDNA PCR products. Although sequence analysis showed differing bacterial communities across time and between the different windrows, similarities in the progression were noted. The majority of sequences recovered from the first sampling period (day 1) were highly similar to previously isolated organisms. The clone libraries from the last sampling period (day 106) contained organisms that showed lower homology to their closest relatives, often with other uncultured organisms, and in phyla that contain few cultured representatives. These data suggest that specific respiratory activity may be an important driver of bacterial diversity in composting environments.     

Modification of soil humic matter after 4 years of compost application

Two soil plots, 1 ha each, were amended yearly for 4 years, respectively, with 35.8 and 71.6 Mg ha(-1) yr(-1) of mature compost (CM) obtained from food and vegetable residues. The compost, amended soils, and a control soil plot after 4 years (S4), were analyzed for humin (HUC), humic acid (HAC), fulvic acid (FAC), and non-humic carbon (NHC) content. Compared to S4, the amended soil contained more humified C (HAC, FAC and HUC) and less NHC. Further evidence of the effect of compost on soil organic matter was obtained by the analysis of the humic acid (HA) fractions isolated from both the compost and the soils. These were characterized by elemental analyses and Diffuse Reflectance Infrared Fourier Transformed spectroscopy. The HAs isolated from CM and from S4 were significantly different. The HAs isolated from the amended plots were more similar to HA isolated from CM than to HA isolated from S4. The experimental data of this work indicate that the compost application may affect significantly the soil organic matter composition, and that the approach used in this work allows one to trace the fate of compost organic matter in soil.     

The effect of carbonate and biochar on carbon and nitrogen losses during composting

Journal of Material Cycles and Waste Management - Limited options and high prices have limited the application of additives in composting. The effect of applying carbonate (SRC) and biochar (BC) to...     

A comparison of mesophilic composting and unamended land treatment for the bioremediation of aged tar residues in soil

A field study was conducted to compare the effectiveness of land treatment and mesophilic composting in removing aged polycyclic aromatic hydrocarbons (PAH) from soil. The soil composting treatment, which had 20 percent (w/w) fresh organic matter incorporated into the soil, reached mesophilic temperatures of 45 to 50°C at week 3–4 and was effective in reducing PAH from 2240 mg/kg to 120 mg/kg after 224 days of treatment. Conventional land treatment with and without added cow manure (5 percent w/w) was less effective in removing the PAH from the soil than was the mesophilic soil composting treatment. In a parallel laboratory trial, PAH concentrations were reduced below 500 mg/kg (the target cleanup concentration for the site) when the contaminated soil was amended with 20 to 30 percent (w/w) fresh organic matter after 186 days of treatment. PAH degradation was lower in the laboratory trial compared with the field trial and no self-heating of soil was demonstrated in the laboratory. Based on the relatively high total heterotrophic and naphthalene-degrading microbial populations in the nonsterile treatments, it was apparent that the absence of microorganisms was unlikely to have limited the biodegradation of PAH in the current study. Fresh organic matter amendments of green tree waste and cow manure, regular mixing of the compost, and maintenance of moisture by regular watering were critical factors in achieving the target PAH concentrations.     

Degradation and environmental risk of surfactants after the application of compost sludge to the soil

In this work, the degradation of anionic and non-ionic surfactants in agricultural soil amended with sewage sludge is reported. The compounds analysed were: linear alkylbenzene sulphonates (LAS) with a 10-13 carbon alkylic chain, and nonylphenolic compounds (NPE), including nonylphenol (NP) and nonylphenol ethoxylates with one and two ethoxy groups (NP1EO and NP2EO). The degradation studies were carried out under winter (12.7°C) and summer (22.4°C) conditions in Andalusia region. The concentration of LAS was reduced to 2% of the initial concentration 100 day after sludge-application to the soil. The half-life time measured for LAS homologues were ranged between 4 and 14days at 12.7°C and between 4 and 7 days at 22.4°C. With regard to NPE compounds, after 8 and 4days from the beginning of the experiment at 12.7 and 22.4°C, respectively, their concentration levels were increased to 6.5 and 13.5mg/kgdm (dry matter) as consequence of the degradation of nonylphenol polyethoxylates. These concentration levels were reduced to 5% after 63 and 70 days for 12.7°C and 22.4°C, respectively. The half-life times measured for NPEs were from 8 to 16 days at 12.7°C and from 8 to 18 days at 22.4°C. Environmental risk assessment revealed that for LAS homologues no environment risk could be expected after 7 and 8 days of sludge application to the soil for 22.4 and 12.7°C, respectively; however, potential toxic effects could be observed for the nonylphenolic compounds during the first 56 days after sludge application to the soil.     

Review of in situ remediation technologies for lead,zinc, and cadmium in soil

This article presents a review of in situ technologies for the remediation of soils contaminated with lead, zinc, and/or cadmium. The objective of this review is to assess the developmental status of the available in situ technologies and provide a general summary of typical applications and limitations of these technologies. The literature review identified seven in situ remediation technologies—solidification/stabilization, vitrification, electrokinetic remediation, soil flushing, phytoextraction, phytostabilization, and chemical stabilization. These technologies were considered for their ability to meet a specific set of remediation objectives under a range of conditions. Each of these technologies has both strengths and weaknesses for addressing particular remedial situations discussed in the article for each of the technologies. A general summary of which technologies are most applicable to common remedial scenarios is also provided. © 2004 Wiley Periodicals, Inc.     

Methane and carbon dioxide emission in a two-phase olive oil mill sludge windrow pile during composting

The aim of this work was to make some preliminary evaluations on CO(2) and CH(4) emissions during composting of two-phase olive oil mill sludge (OOMS). OOMS, olive tree leaves (OTL) and shredded olive tree branches (OTB) were used as feedstock for Pile I and Pile II with a 1:1:1 and 1:1:2v/v ratio, respectively. Each pile was originally 1.2m high, 2.0m wide and approximately 15.0m long. Four 500 ml volume glass funnels were inverted and introduced in each pile, two in the core (buried 50-60 cm from the surface) and two near the surface under a thin 10-15 cm layer of the mixture. Thin (0.5 cm diameter) plastic, 80 cm long tubes were connected to the funnels. A mobile gas analyser (GA2000) was used to measure the composition (by volume) of O2, CO2 and CH4 on a daily basis. The funnels were removed prior to each turning and reinserted afterwards. From each pair of funnels (core and surface) of both piles, one was kept closed between samplings. Two way ANOVA was used to test differences between piles and among the tubes. Post hoc Tukey tests were also used to further investigate these differences. There was a significant difference (at p<0.001) in the two piles for all three gases. The average concentrations of O2, CO2 and CH4 in Pile I, from all four funnels was 16.86%, 3.89% and 0.25%, respectively, where for Pile II the average values were 18.07%, 2.38% and 0.04%, respectively. The presence of OOMS in larger amounts in Pile I (resulting in more intense decomposing phenomena), and the larger particle size of OTB in Pile II (resulting in increasing porosity) are the probable causes of these significant differences. Samples from open funnels presented lower, but not significantly lower, O2 composition (higher for CO2 and CH4) in comparison with closed funnels in both depths and both piles. Not significant were also the different mean gas compositions between core and surface funnels in the same pile.     

Characterization and modelling of the heat transfers in a pilot-scale reactor during composting under forced aeration

The paper focused on the modelling of the heat transfers during composting in a pilot-scale reactor under forced aeration. The model took into account the heat production and the transfers by evaporation, convection between material and gas crossing the material, conduction and surface convection between gas and material in bottom and upper parts of the reactor. The model was adjusted thanks to the measurements practised during fifteen composting experiments in which five organic wastes were, each, composted under three constant aeration rates. Heat production was considered proportional to oxygen consumption rate and the enthalpy per mole oxygen consumed was assumed constant. The convective heat transfer coefficients were determined on basis of the continuous measurements of the temperatures of both the lid and the bottom part of the reactor. The model allowed a satisfying prediction of the temperature of the composting material. In most cases, the mean absolute discard between the experimental and the simulated temperatures was inferior to 2.5°C and the peaks of temperature occurred with less than 8h delay. For the half of the experiments the temperature discard between the simulated peak and the experimental one was inferior to 5°C. On basis of the calculation of a stoichiometric production of water through oxidation of the biodegradable organic matter, the simulation of water going out from material as vapour also allowed a rather satisfying prediction of the mass of water in final mixture. The influence of the aeration rate on every type of heat loss was characterized. Finally, the model was used to evaluate the impacts on material temperature caused by the change of the insulation thickness, the ambient temperature, take the lid away, the increase or the decrease of the mass of waste to compost.