Recycling of Two-Phase Olive-Mill Cake “Alperujo” by Co-composting with Animal Manures

The use of poultry manure or goat/sheep manure in the co-composting of the two-phase olive-mill cake “alperujo” (ALP) with olive leaf (OL) is compared by studying organic-matter mineralization and humification processes during composting and the characteristics of the end products. For this, two different piles (P1 and P2) were prepared using ALP with OL mixed with poultry manure (PM) and goat/sheep manure (GSM), respectively, and composted by the turned windrow composting system. Throughout the composting process, a number of parameters were monitored, such as temperature, pH, electrical conductivity (EC), organic matter (OM), OM losses, total organic carbon (C_org), total nitrogen (N_t), C_org/N_t ratio, and the germination index (GI). In both piles, the temperature exceeded 55 °C for more than 2 weeks, which ensured maximum pathogen reduction. Organic-matter losses followed a first-order kinetic equation in both piles. The final composts presented a stabilized OM and absence of phytotoxins, as observed in the evolution and final values of the C_org/N_t ratio (C_org/N_t < 20) and the germination index (GI > 50 percent). Therefore, composting can be considered as an efficient treatment to recycle this type of waste, obtaining composts with suitable properties that can be safely used in agriculture.     

Assessment of maturity degree of composts from domestic solid wastes by fluorescence and Fourier transform infrared spectroscopies.

Methods of assessment of compost maturity are needed so the application of composted materials to lands will provide optimal benefits. The aim of the present paper is to assess the maturity reached by composts from domestic solid wastes (DSW) prepared under periodic and permanent aeration systems and sampled at different composting time, by means of excitation-emission matrix (EEM) fluorescence spectroscopy and Fourier transform infrared spectroscopy (FT-IR). EEM spectra indicated the presence of two different fluorophores centered, respectively, at Ex/Em wavelength pairs of 330/425 and 280/330 nm. The fluorescence intensities of these peaks were also analyzed, showing trends related to the maturity of composts. The "contour density" of EEM maps appeared to be strongly reduced with composting days. After 30 and 45 days of composting, FT-IR spectra exhibited a decrease of intensity of peaks assigned to polysaccharides and in the aliphatic region. EEM and FT-IR techniques seem to produce spectra that correlate with the degree of maturity of the compost. Further refinement of these techniques should provide a relatively rapid method of assessing the suitability of the compost to land application.     

Physicochemical,including spectroscopic,and biological analyses during composting of green tea waste and rice bran

The aims of this study were to monitor the changes in physicochemical, including spectroscopic, and biological characteristics during composting of green tea waste–rice bran compost (GRC) and to define parameters suitable for evaluating the stability of GRC. Compost pile temperature reflected the initiation and stabilization of the composting process. The pH, electrical conductivity, NO₃ ⁻-N content, and carbon-to-nitrogen ratio were measured as chemical properties of the compost. The color (CIELAB variables), humification index (the absorption ratio Q _4/6 = A ₄₇₂ / A ₆₆₄ of 0.5 M NaOH extracts), absorption at 665 nm of acetone extracts, and Fourier-transform infrared (FT-IR) spectra were measured to evaluate the organic matter transformation; germination of komatsuna or tomato seeds was measured to assess the potential phytotoxicity of composting materials during composting. No single parameter was capable of giving substantial information on the composting process, the nutrient balance, phytotoxicity, and organic matter decomposition. The FT-IR spectra at 3,300, 2,930, 2,852, and 1,065 cm⁻¹ provided information on the molecular transformation of GRC during composting and they decreased over the composting. Most of the assayed parameters showed no further change after about 90 days of composting suggesting that GRC can be used for agricultural purposes after this period.     

UV–Visible and Fluorescence Green Waste Composts Monitoring: Material Dependency

ABSTRACT

The most frequent way to survey green waste composts is to monitor the temperature during the composting process. However, if the temperature is a good index for global biological processes, it is not for the chemical stability. In order to identify a reliable index, this work investigates water extraction coupled to spectroscopic indexes such as E₂/E₃, E₄/E₆, and SUVA₂₅₄ ratios, and fluorescence indexes such as Kalbitz, Milori, CP/PARAFAC, and Fluorescence Region Integration. The measurements of these indexes are carried out with six samples from different sites with different green waste material composition. The results show that most indexes depend on the green waste origin more than the composting time; some depend mostly on the material origin while others on compost age. A comparison of these results indicates that the biochemical process occurs more rapidly than expected by the compost producers. The combination of these indicators gives useful information on the processes that take place during composting.     

黑土、潮土和红壤可溶性有机质的光谱特征及结构差异

为探究不同类型土壤可溶性有机质(DOM)含量和结构的差异性,选取黑土、潮土和红壤3种土壤的表层土壤(0~20 cm)为研究对象,提取其中的DOM,应用紫外–可见光谱、荧光光谱等技术,分析土壤中DOM的数量和光谱特征。结果显示:3种不同类型土壤中可溶性有机碳(DOC)含量及其与土壤有机碳(SOC)的比值(SOC/DOC)大小为:红壤>黑土>潮土(P<0.05);A254值大小为黑土>潮土>红壤,但SUVA254值大小为:潮土>黑土>红壤(P<0.05),表明潮土DOM的芳香化程度最高,但芳香性结构物质含量低于黑土DOM,红壤DOM的芳香性结构物质含量和芳香性构化程度均低于黑土和潮土DOM;荧光发射光谱腐殖化指数(HIXem)和荧光效率(Feff)值大小为:红壤>黑土>潮土(P<0.05),说明红壤DOM的腐殖化程度和π电子共轭基团含量比潮土和黑土DOM高;荧光指数(FI)大小为:红壤>潮土>黑土(P<0.05),表明红壤DOM比潮土和黑土DOM含有更多的微生物源组分;荧光同步光谱显示,黑土和潮土DOM以类蛋白质基团为主,红壤DOM以木质素类基团为主;在土壤有机质含量、黏粒含量和黏土矿物种类不同的情况下,土壤对DOM的吸附能力不同,使土壤DOM的提取比例也存在显著差异。     

Evaluation of Parameters During Composting of Two Contrasting Raw Materials

The aims of this work were: i) to evaluate, during a composting process, some parameters in two contrasting raw materials: one a ligneous material (C1) and the other (C2) a mixture of horse and poultry manure with a low straw percentage and ii) to compare results from microbiological and chemical analyses of both composting material during the process. Total carbon, total nitrogen, C: N ratio, ash, organic matter, organic matter destroyed, CEC, soluble organic carbon, soluble ammonium and nitrate, ammonium: nitrate ratio and respiration rate were evaluated during 18 weeks. C1 material showed a lower rate of organic matter mineralization probably due to the high proportion of ligneous material. This material reached a greater CEC during the experiment. Increase in CEC during composting is due to conversion of the remaining organic material into humic substances. These results would imply that C1 presented a greater humification level and consequently, a better quality. On the other hand, the greater decrease in soluble organic carbon and NH₄⁺-N values in C2 is in accordance with greater organic matter mineralization. A high decrease in soluble fractions, especially the more degradable ones (water soluble components) indicates a high mineralization of the organic matter during composting and a lower humification level. According to the data obtained in our experiment, some parameters such as CEC, soluble organic carbon and soluble NH₄⁺-N seem to achieve the stability level for both studied materials, while those parameters or indices such as C: N ratio, NH₄⁺-N: NO₃^?-N ratio indicated stability/maturity only in C2 material during the experimental time.     

Chemical and microbiological parameters for the characterisation of the stability and maturity of pruning waste compost

Composting of pruning waste, leaves and grass clippings was monitored by different parameters. A windrow composting pile, having the dimensions 2.5 m (height) x 30 m (length) was establish. The maturation of pruning waste compost was accompanied by a decline in NH₄ ⁺-N concentration, water soluble C (WSC) and an increase in NO₃ ^–-N content. Both organic matter (OM) content and total N (TN) losses during composting followed a first-order kinetic equation. These results were in agreement with the microbiological activity measured either by the CO₂ respiration or dehydrogenase (DH-ase) activity during the process. Statistically significant correlations were found between DH-ase activity, easily biodegradable organic C forms, NH₄ ⁺-N and NO₃ ^–-N concentrations and organic matter content and N losses. For this reason, DH-ase activity and the CO₂ evolution could be used as good indicators of pruning waste compost maturity. In contrast, humification parameters data from the organic matter fractionation did not agree with the initially expected values and did not contribute to the assessment of compost maturity. Neither the cation exchange capacity nor the germination index showed a clear tendency during the composting time, suggesting that these parameters are not suitable for evaluating the dynamics of the process.     

The Influence of Humification Degree of Humic Acid on Its Sorption of Norfloxacin During Sewage Sludge Composting

Norfloxacin (NOR), an antibiotic widely used in livestock and poultry production, has become ubiquitous in the aquatic and terrestrial ecosystems as a result of veterinary excretion of the parent compound or its active metabolites. The sorption of NOR onto humic acid (HA) may influence the fate of NOR in the environment. In the present study, HA was extracted from sewage sludge in different composting stages of days 0, 10, 30, and 70 to investigate the sorption of NOR onto HA as affected by the humification degree of HA. The results of elemental and Fourier transform infrared (FTIR) spectrum analyses showed that the contents of aromatic and carboxylic groups in HA increased with composting time, indicating an increase of humification degree. The result of sorption experiments demonstrated that the HA had a high sorption capacity for NOR with strong nonlinearity. A two-stage sorption was observed in the sorption process with an equilibration time of 48 h. Both the Freundlich model (Adj. R² range 0.988–0.994) and Langmuir model (Adj. R ² range 0.917–0.928) fitted well with all sorption isotherms of the HA samples of different humification degrees. Moreover, the increase of sorption distribution coefficient (K _d ) value with composting time indicated that the sorption affinity of HA for NOR increased with increasing humification degree of HA. The major sorption mechanism was the interaction between NOR and rich aromatic moieties and carboxylic group in the HA.     

Uncomposted Sheep and Cow Manures as a Source of Commercial Humic Amendments: An Exploratory Study

Liquid humic amendments are widely used in many countries as an enhancer of crop production (particularly root growth). While leonardite is the main substrate for obtaining these products, there is growing concern about obtaining them from plant-derived residual materials, rich in lignin and polyphenolics, thus making possible a residue valorization. Composting is a necessary step for converting these residues into a source of humic substances. In arid countries, obtaining humic products from sources other than leonardite faces two main challenges: (i) often such countries are devoid of forested areas or tree crops capable of supplying lignin-rich residues in large amounts and (ii) water is scarce (or very expensive if obtained by desalination) and therefore composting on an industrial scale is very difficult. Thus it is essential to find alternative sources capable of yielding humic or humic-like compounds without any previous composting. Here we present the main results obtained using sheep and cow manure, two materials widely available in the Kingdom of Saudi Arabia (KSA). Both were extracted using potassium hydroxide (KOH) at a variety of concentrations (from 0.25 to 2 M), times (from 20 to 120 min), temperatures (from 100 to 150 °C), and pressures. Sheep manure, much easier to extract than cow manure, appears the more promising as a source of commercial humic amendments. No lengthy extraction times are needed to obtain alkaline extracts; 20 min yields only slightly less humic-like matter than 2 h. The relative abundance of humic-like substances in the extract tends to decrease with time, but some optical indicators of humification (E₄/E₆ ratio, absorption at 280 nm, ratios of absorption at 253/203 and 253/220 nm) tend to increase. Polysaccharides, the dominant form of organic matter in the original manure, strongly resist alkaline extraction: their prior hydrolysis may be necessary to increase the yields of humic-like matter from the studied manures.     

Fluorescence spectroscopy of aqueous pine litter extracts: effects of humification and aluminium complexation

Fluorescence excitation, emission, and synchronous-scan spectra were obtained for aqueous extracts of needle and litter layer (O-horizon) samples from ponderosa pine collected at a plantation site. The spectral lineshapes differed markedly between the needle and litter samples, and showed an increasing overall intensity with increasing extent of humification (increasing depth in the litter layer). At a dissolved organic C (DOC) concentration of 100 g m^?3, these effects were accompanied by a general shift in spectral density from lower to higher wavelength such that, in the excitation spectra, there was increasing prominence of a peak at 390 nm. When the DOC concentration was decreased from 100 to 25 g m^?3, the overall spectral intensity decreased and the peak at 390 nm in the excitation spectra of the litter samples gave way to a rising peak at 340 nm. Changes in pH from 4 to 5, characteristic of the undiluted litter extracts, produced little effect on the spectra. The addition of A1 at 40 mmol m^?3 generally produced enhancement of the fluorescence intensity in all three kinds of spectra for the needle and upper litter-layer extracts at 100 g C m^?3 and pH 4. Spectral density below 320 nm in the excitation and synchronous-scan spectra of the needle solution (possibly attributable to gentisic acid on the basis of model experiments) was, however, diminished by Al addition. For the lower litter-layer extracts, A1 addition decreased the fluorescence intensity in excitation and emission spectra, whereas it increased the intensity in synchronous-scan spectra. These trends indicated that the water-soluble fluorophores in the litter layer differed significantly from those in the fresh needles, and changed with the extent of humification. The 390-nm peak in the excitation spectrum, particularly its behaviour in the presence of added Al, may be useful as a spectral signature of products formed by litter humification processes.     

Evaluation of maturity and stability parameters of composts prepared from farm wastes

A composting experiment was carried out to study changes in physical [color, odor, temperature, organic matter (OM) loss], chemical [C:N ratio, water-soluble organic carbon (C_w):organic N (N_org) ratio, NH₄ ⁺-N and NO₃ ^?-N, humic acid (HA):fulvic acid (FA) ratio, humification index (HI) and cation-exchange capacity (CEC):total organic carbon (TOC) ratio)] and biological [seed germination index (GI)] parameters to assess compost maturity and stability over a period of 150 days. Five composts were prepared using a mixture of different farm wastes with or without enrichment of N, rock phosphate (RP) and microorganism (MO) inoculation. All the composts appeared to change to a granular and dark grey color without foul odor, and attained a constant temperature with no measurable changes (ambient level) at 120 days of composting. Correlation analysis showed that the optimal values of the selected parameters for our experimental conditions are as follows: organic matter loss > 42%, C:N ratio < 15, HA:FA ratio > 1.9, HI > 30%, CEC:TOC ratio > 1.7 and C_w:N_org ratio < 0.55. Composts enriched with N + RP or N + RP + MO matured at 150 and 120 days, respectively, whereas composts without any enrichment or enrichment with N or RP + MO did not mature even at 150 days of composting.     

Assessment of Biotransformation of Sludge from Vegetable Oil Refining by Composting

The evolution of organic matter of sludge from vegetable oil refining (50%) mixed with turf (40%) and straw (10%) during 6 months of composting was evaluated by physicochemical and spectroscopy analysis. The intense microbial activity is characterized by a significant increase in temperature (over 67°C) during the thermophilic phase (7 days). The final product is characterized by a decomposition rate of 50, C/N ratio about 12, NH₄⁺/NO₃^? ratio less than 1, and a neutral pH. The lipid analysis showed that total lipids decreased by 83% as a result of biodegradation of lipid compounds of the composted substrate. The degree of polymerization during composting is of about 16%, which provides information on the success of the process. The spectroscopic analysis showed a decrease of the ratios E4/E6 and E2/E6, which clearly shows the humification of organic matter. The physicochemical and spectroscopy parameters of the mixture show the stability and maturity of the final compost, which is confirmed by the germination index (60% for lettuce and turnips, and 90% for cress and lucerna). The results of the evolution of sludge from vegetable oil refining mixed with green wastes produced a mature product that can be applied in agriculture.     

Carbon and Nitrogen Mineralization and Humus Composition Following Municipal Solid Waste Compost Addition to Laterite Soils under Continuous Cassava Cultivation

A glasshouse incubation experiment was conducted to study the carbon (C) and nitrogen (N) mineralization of municipal solid waste compost (MSWC) added at differential rates to a laterite soil where cassava has been continuously cultivated for the past 10 years. The rate of C mineralization from added substrates increased with increasing rates of addition of MSWC. Available N significantly increased with increase in the rate of application of MSWC. There was a decreasing trend in E₄₆₅/E₆₆₅ ratio of humic acid as we increased the rate of application of MSWC from 2.5 to 20 t ha^?1. The Cross Polarization Magic Angle Spinning (CPMAS) ¹³C NMR spectral analysis revealed that there are differences in the rate of humification of added MSWC, and application of MSWC at 15 t ha^?1 resulted in least humification with the greatest alkyl C, lowest aromatic C, and greater O-alkyl C content. The decomposition rate (R) was found to be greater for this treatment. The residual C in soil was found to increase over time coincident with greater rates of MSWC application, indicating increased C stabilization, which could improve soil quality.     

Carbon and nitrogen transformation during composting of sweet sorghum bagasse

Two types of compost, consisting of sweet sorghum bagasse with either sewage sludge or a mixture of pig slurry and poultry manure, were studied in a pilot plant using the Rutgers system. The total degradation of the piles as determined by the weight loss of organic matter during the bio-oxidative and maturation phases accounted for 64% of the organic matter applied and followed a first-order kinetic function. Concentrations of total and organic N increased during the composting process as the degradation of organic C compounds reduced the compost weight. Losses of N through NH₃ volatilization were low, particularly in the compost with sewage sludge due to pH values of <7.0 and the low temperatures reached in the compost during the first 2 weeks. The C:N ratio in the two composts decreased from 24.0 and 15.4 to values between 12 and 10. Increases in cation exchange capacity and in fulvic and humic acid-like C revealed that the organic matter had been humified during composting. The humification index, the C:N ratio, fulvic:humic acid-like C, and cation exchange capacity proved to be the most suitable parameters for assessing the maturity of these composts.     

Changes in Properties of Composting Rice Husk and Their Effects on Soil and Cocoa Growth

The worldwide production of rice husk, a by‐product and agrowaste that causes serious environmental problems, may reach 116 million t y^?1. The objectives of this study were (i) to determine the physicochemical changes of rice husk and its structural chemistry during composting using ¹³carbon nuclear magnetic resonance (¹³C NMR) and (ii) to determine the effect of the composted rice husk (CRH) on the properties of Oxisol and cocoa (Theobroma cacao L.) growth under glasshouse conditions. Results showed an active composting phase occurred at the first 53 days as revealed by high carbon dioxide (CO₂)‐C (40–71 µg g^?1 h^?1) production, followed by a matured composting phase occurring at 54–116 days as revealed by decreasing in CO₂‐C production (10 µg g^?1 h^?1). The active composting was accompanied by increases in electrical conductivity (EC), pH, ammonium (NH₄ ⁺), and nitrate (NO₃), whereas during the matured composting phase, the EC and cation exchange capacity increased but pH, NH₄ ⁺, and NO₃ ^?1 decreased. The ash of the produced compost contains mainly calcium (Ca), potassium (K), sulfur (S), magnesium (Mg), and phosphorus (P) as essential nutrients. The CP/MAS ¹³C NMR spectra before and after various composting times indicated the dominance of sharp and well‐resolved signal peaks at O‐alkyl C and di‐O‐alkyl C regions (67–73%), which are characteristic of cellulose. The percentage of N‐alky/methoxyl was 23–26% whereas phenolic, carboxyl, and alkyl C types were less than 3% each. The application of the CRH to an Oxisol significantly increased soil pH and Ca, Mg, K, sodium (Na), and silicon (Si) ions of in situ soil solution but decreased the amounts of toxic ions [aluminum (Al), manganese (Mn), and iron (Fe)]. The CRH was found to increase cocoa growth up to 37%.     

Evolution of Biochemical Parameters During Composting of Urban Wastes

An experiment was performed for evaluating the most suitable biochemical parameters to measure dynamics of substrate transformation during composting of the organic fraction derived from preselected urban wastes and wood bark mixture. Changes of chemical (organic C, hydrosoluble sugars, total and mineral N, humified fraction, volatile acids and phenolic compounds) and biochemical (microbial respiration, biomass C, qCO₂, dehydrogenase, catalase, urease activities, FDA, and BIF) parameters were monitored for 120 days. Limited changes in organic C, total nitrogen, and humification characteristics were observed during composting. Dehydrogenase and catalase activities, BIF and FDA showed small changes during composting. Urease activity and, with some limitations regarding the early stages of composting, microbial respiration and qCO₂, were found to be the most suitable parameters to measure dynamics of substrate transformation during composting of preselected urban wastes.     

Enzymatic activity as a parameter for the characterization of the composting process

Enzymatic activity (EA) was explored as a possible tool for composting characterization. Three composts (yard wastes, cotton wastes and a mixture of the two) were sampled during different phases of the process and divided in two fractions. The first was immediately analysed for microbial biomass C (B_C) and EAs (β-glucosidase, arylsulphatase, acid and alkaline phosphatase). The second fraction was air-dried prior to analysis for the same EAs and for organic C (C_ORG), total N (N_TOT), dissolved organic C (DOC), extractable C (C_E) and humic-like C (C_H).B_C decreased throughout the composting period (149 days), whereas EA in moist fractions stabilized between 50 (β-glucosidase, alkaline phosphatase) and 90 (arylsulphatase, acid phosphatase) days of composting.EA was always reduced by air‐drying (β-glucosidase: 40-80%; arylsulphatase: 10-50%; acid phosphatase: 10-70%; alkaline phosphatase: 50-90%), but this effect was less prominent as composting proceeded, especially for β-glucosidase and alkaline phosphatase.EA in air-dried samples displayed the same trend as in moist ones, except that there was a marked difference (47-66%) between initial and final activities of all four enzymes.EAs in air‐dried compost and content of humic-like substances showed a similar trend: a marked increase in the first 90 days of the process and no significant variations afterwards. This suggests that the formation of humic-enzymatic complexes has taken place and indicates that this process occurs almost totally during the first stage of composting.EA steadiness in air-dried samples occurred concurrently with the achievement of compost stability, as indicated by the conventional indexes (i.e. C_H, C_ORG/N_TOT). Therefore, the development of a stable enzyme activity in air-dried compost could represent a simple measure of compost stabilization in routine analysis of composting process.     

Transformation of Water-Soluble Organic Substances in Litters of Podzols in the Background and Technogenic Areas of the Kola Peninsula

Mineralization of water-soluble organic substances in forest litters of different compositions under conditions of their pollution with heavy metals from aerogenic emissions is considered. Water-soluble organic substances of the pine forest litters are shown to be less stable than that under the spruce forests irrespective of their pollution; the portion of mineralized at 20°C carbon for a month reached 40%. In the spruce litters, mineralizable amounts of carbon are related to their pollution: in the technogenic areas, compared to the background ones, carbon losses from the litters are twice greater. In the course of decomposition, in the spruce and pine litters, phenol compounds accumulate among the water-soluble organic compounds, and this process is more intense in the contaminated areas. After the decomposition of all the litters, irrespectively of their composition and the distance from the pollution sources, the water-soluble organic substances are characterized by higher indices of humification (HIX), more intense fluorescence, and greater coefficients of specific extinction (E₂₆₀). In the ultraviolet spectra, bands appear in the region of aromatic amines absorption. These changes indicate the transformation of water-soluble organic substances: the degrees of their condensation and aromaticity increase and nitrogen-containing aromatic compounds are formed.     

Evaluation of sewage sludge-based compost by FT-IR spectroscopy

The aerobic batch composting fermentations of sewage sludge with wood chips and maturity compost as co-composting additives were carried out in an open type lab-scale reactor. Fourier transform infrared spectroscopy (FT-IR) spectroscopy was used to monitor the composting process, evaluate the degradation rate and thus determine the maturity. Although the composition of the input mixture strongly affects the shape of the infrared (IR) spectra, typical bands of components can be selected and used to follow the composting process.

The appearance, shape and intensity of the nitrate band at 1384 cm^− 1 was well pronounced and evident for a sewage sludge-based compost maturity. An increase of the peak ratio 1384 / 2925 and decrease of 2925 / 1034, 1034 / 1384 correlated with the degree of decomposition. For the composting mixture under study the peak ratios 1034 / 1384 and 1384 / 2925 were more demonstrative. Considering the influence of the composting mixture (components and their ratio) on the shape of the FT-IR spectra the nitrate band at 1384 cm^− 1 can be overlapped by other absorption bands (e.g. lignin bands in 1300–1400 cm^− 1 region) thus appearing in the spectra as a shoulder, and therefore the ratios 1384 / 2925 and 1034 / 1384 become unusable to evaluate the maturity.

FT-IR spectroscopy is a quick and useful method to monitor the composting process; however any particular composting mixture needs preliminary studies of the spectra. Consequently, the most appropriate criteria describing the process (e.g. band ratios, shape and intensity of nitrate band) should be selected and the time / peak ratio curves recorded for a compost mixture under study. Afterwards monitoring of the composting process can be based on the comparison of the controls and definite samples.