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Increasing water pollution and decreasing energy reserves have emerged as growing concerns for the environment. These pollution are due to the dangerous effects of numerous pollutants on humans and aquatic organisms, such as hydrocarbons, biphenyls, pesticides, dyes, pharmaceuticals, and metal ions. On the other hand, the need for a clean environment, finding alternatives to fossil and renewable fuels is very important. Hydrogen (H2) is regarded as a viable and promising substitute for fossil fuels, and a range of methodologies have been devised to generate this particular source of energy. Metal-organic frameworks (MOFs) are a new generation of nanoporous coordination polymers whose crystal structure is composed of the juxtaposition of organic and inorganic constituent units. Due to their flexible nature, regular structure, and high surface area, these materials have attracted much attention for removing various pollutants from water and wastewater, and water splitting. MOFs Z-scheme heterojunctions have been identified as an economical and eco-friendly method for eliminating pollutants from wastewater systems, and producing H2. Their low-cost synthesis and unique properties increase their application in various energy and environment fields. The heterojunctions possess diverse properties, such as exceptional surface area, making them ideal for degradation and separation. The development and formulation of Z-scheme heterojunctions photocatalytic systems using MOFs, which possess stable and potent redox capability, have emerged as a successful approach for addressing environmental pollution and energy shortages in recent times. Through the utilization of the benefits offered by MOFs Z-scheme heterojunctions photocatalysts, such as efficient separation and migration of charge carriers, extensive spectrum of light absorption, among other advantages, notable enhancements can be attained. This review encompasses the synthesis techniques, structure, and properties of MOFs Z-scheme heterojunctions, and their extensive use in treating various wastewaters, including dyes, pharmaceuticals, and heavy metals, and water splitting. Also, it provides an overview of the mechanisms, pathways, and various theoretical and practical aspects for MOFs Z-scheme heterojunctions. Finally, it thoroughly assesses existing challenges and suggests further research on the promising applications of MOFs Z-scheme in industrial-scale wastewater treatment.
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Adsorbents synthesized by activation and nanoparticle surface modifications are expensive and might pose health and ecological risks. Therefore, the interest in raw waste biomass materials as adsorbents is growing. In batch studies, an inexpensive and effective adsorbent is developed from raw olive stone (OS) to remove methylene blue (MB) from an aqueous solution. The OS adsorbent is characterized using scanning electron microscopy (SEM), Fourier Transform Infra-Red (FTIR), and Brunauer-Emmett-Teller (BET) surface area. Four isotherms are used to fit equilibrium adsorption data, and four kinetic models are used to simulate kinetic adsorption behavior. The obtained BET surface area is 0.9 m2 g-1, and the SEM analysis reveals significant pores in the OS sample that might facilitate the uptake of heavy compounds. The Langmuir and Temkin isotherm models best represent the adsorbtion of MB on the OS, with a maximum monolayer adsorption capacity of 44.5 mg g-1. The best dye color removal efficiency by the OS is 93.65% from an aqueous solution of 20 ppm at the OS doses of 0.2 g for 90 min contact time. The OS adsorbent serves in five successive adsorption cycles after a simple filtration-washing-drying process, maintaining MB removal efficiency of 91, 85, 80, and 78% in cycles 2, 3, 4, and 5, respectively. The pseudo second-order model is the best model to represent the adsorption process dynamics. Indeed, the pseudo second-order and the Elovich models are the most appropriate kinetic models, according to the correlation coefficient (R2) values (1.0 and 0.935, respectively) derived from the four kinetic models. The parameters of the surface adsorption are also predicted based on the mass transfer models of intra-particle diffusion and Bangham and Burt. According to the thermodynamic analysis, dye adsorption by the OS is endothermic and spontaneous. As a result, the OS material offers an efficient adsorbent for MB removal from wastewater that is less expensive, more ecologically friendly, and economically viable.
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This study evaluated the application and efficiency of modified activated carbon in the removal of copper (Cu) from synthetic aquatic samples. The surface of activated carbon derived from orange peel (AC-OP) and date seeds (AC-DS) have been modified by Titanium dioxide nanoparticles (TiO2 NPs) (1:10 wt% mixing ratio) and used in a series of experiments designed by Response Surface Methodology (RSM) incorporating Central Composite Design (CCD). The Brunauer-Emmett-Teller (BET) test demonstrated that the modification has increased the surface area of AC-OP from 2.40 to 6.06 m2 g-1 and AC-DS from 51.10 to 81.37 m2 g-1. Effects of pH (1-7), ion initial concentration (10-60 mg L-1), adsorbent dose (0.5-8 g L-1), and contact time (0.4-6 h) have been investigated. The results showed that the optimum conditions for TiO2-modified AC-OP (OP-TiO2) are pH 5, initial concentration of 24.6 mg L-1, adsorbent dose of 4.9 g L-1, and contact time of 3.6 h. The optimum conditions for TiO2-modified AC-DS (DS-TiO2) are pH 6.4, initial concentration of 21.2 mg L-1, adsorbent dose of 5 g L-1, and contact time of 3.0 h. The modified quadratic models represented the results well with regression coefficients of 0.91 and 0.99 for OP-TiO2 and DS-TiO2, respectively. The maximum Cu removal for OP-TiO2 and DS-TiO2 were 99.90 % and 97.40 %, and the maximum adsorption capacity was found to be 13.34 and 13.96 mg g-1, respectively. Kinetic data have been fitted to pseudo first-order, pseudo second-order, intra-particle diffusion, and Elovich models. The pseudo second-order showed a better fit to the experimental data (R2 > 98 %). This study demonstrates the successful development of modified activated carbon derived from orange peels and date seeds, modified by TiO2 nanoparticles, for efficient adsorption of copper ions from water. The findings contribute to understanding the adsorption mechanism and provide valuable insights for designing environmentally friendly adsorbents.
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In this work, the MCM-48 mesoporous material was prepared and characterized to apply it as an active adsorbent for the adsorption of 4-nitroaniline (4-Nitrobenzenamine) from wastewater. The MCM-48 characterizations were specified by implementing various techniques such as; scanning electron microscopy (SEM), Energy dispersive X-ray analysis (EDAX), X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area, pore size distribution (PSD), and Fourier transform infrared (FTIR). The batch adsorption results showed that the MCM-48 was very active for the 4-nitroaniline adsorption from wastewater. The adsorption equilibrium results were analyzed by applying isotherms like Langmuir, Freundlich, and Temkin. The maximum experimental uptake according to type I Langmuir adsorption was found to be 90 mg g-1 approximately. The Langmuir model with determination coefficient R2 = 0.9965 is superior than the Freundlich model R2 = 0.99628 and Temkin model R2 = 0.9834. The kinetic adsorption was investigated according to pseudo 1st order, pseudo 2nd order, and Intraparticle diffusion model. The kinetic results demonstrated that the regression coefficients are so high R2 = 0.9949, that mean the pseudo 2nd order hypothesis for the adsorption mechanism process appears to be well-supported. The findings of adsorption isotherms and kinetics studies indicate the adsorption mechanism is a chemisorption and physical adsorption process.
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Aguas Residuales , Contaminantes Químicos del Agua , Termodinámica , Adsorción , Contaminantes Químicos del Agua/análisis , Espectroscopía Infrarroja por Transformada de Fourier , Cinética , Concentración de Iones de HidrógenoRESUMEN
This study focused on developing a new cocktail extraction agent (CEA) composed of solvent and a new surfactant material (SM) for enhancing the efficiency of fuel recovery from real waste oil sludge (WSO). The effects of different solvents (e.g. methyl ethyl ketone (MEK), naphtha, petrol and kerosene), SMs (Dowfax and sodium thiosulfate), extraction time (10-20 min), extraction temperatures (20-60 °C) and CEA/sludge ratios (1-4) on the extraction performance were investigated. SMs and DBBE design enhanced the extraction efficiency by increasing the dispersion of solvent in WSO and enhancing the mixing and mass transfer rates. Results proved that Dowfax was the best SM for oil recovery under various conditions. The best CEA (e.g. MEK and Dowfax) provides the maximum fuel recovery rate of 97% at a period of 20 min, temperature of 60 °C and 4:1 CEA/sludge ratio. The produced fuel was analysed and fed to the distillation process to produce diesel oil. The characteristics of diesel oil were measured, and findings showed that it needs treatment processes prior its use as a finished fuel.
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The main challenges of liquid hydrogen (H2) storage as one of the most promising techniques for large-scale transport and long-term storage include its high specific energy consumption (SEC), low exergy efficiency, high total expenses, and boil-off gas losses. This article reviews different approaches to improving H2 liquefaction methods, including the implementation of absorption cooling cycles (ACCs), ejector cooling units, liquid nitrogen/liquid natural gas (LNG)/liquid air cold energy recovery, cascade liquefaction processes, mixed refrigerant systems, integration with other structures, optimization algorithms, combined with renewable energy sources, and the pinch strategy. This review discusses the economic, safety, and environmental aspects of various improvement techniques for H2 liquefaction systems in more detail. Standards and codes for H2 liquefaction technologies are presented, and the current status and future potentials of H2 liquefaction processes are investigated. The cost-efficient H2 liquefaction systems are those with higher production rates (>100 tonne/day), higher efficiency (>40%), lower SEC (<6 kWh/kgLH2), and lower investment costs (1-2 $/kgLH2). Increasing the stages in the conversion of ortho- to para-H2 lowers the SEC and increases the investment costs. Moreover, using low-temperature waste heat from various industries and renewable energy in the ACC for precooling is significantly more efficient than electricity generation in power generation cycles to be utilized in H2 liquefaction cycles. In addition, the substitution of LNG cold recovery for the precooling cycle is associated with the lower SEC and cost compared to its combination with the precooling cycle.
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The objective of this study was to obtain start-up strategies for the operation of a dry anaerobic digestion (DAD) system treating pig-manure (PM) solids at low-temperatures, and evaluate the effects of operation mode, adapted inoculum, and bedding material on the performance. A DAD system coupled with an inoculum system (two-stage DAD) was operated at 20 ± 1 °C to digest PM solids (Total Solids, TS: 27%) with wheat straw or woodchips as bedding materials (TS substrate-mixture: 45%) using a liquid inoculum. Static DAD was also operated in parallel for comparison purposes. Overall, the percolation-recirculation mode of operation was superior to the static mode; the former had more than a 3-fold increase in specific methane yield in cycle 3. Using the adapted inoculum in cycle-2 improved methane yield by 7% and 26% for cycles 1 and 3, respectively, under the percolation-recirculation mode of operation. In addition, the digestate resulting from the digestion of woodchips + PM solids had better physical characteristics than wheat straw + PM solids. Thus, anaerobic digestion of pig-manure solids at low-temperatures with appropriate start-up strategies, inoculum, and bedding material is a promising technology for transforming PM solids into biogas and using its digestate as biofertilizer.
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To assess biohydrogen for future green energy, this review revisited dark fermentation and microbial electrolysis cells (MECs). Hydrogen evolution rate in mesophilic dark fermentation is as high as 192 m3 H2/m3-d, however hydrogen yield is limited. MECs are ideal for improving hydrogen yield from carboxylate accumulated from dark fermentation, whereas hydrogen production rate is too slow in MECs. Hence, improving anode kinetic is very important for realizing MEC biohydrogen. Intracellular electron transfer (IET) and extracellular electron transfer (EET) can limit current density in MECs, which is proportional to hydrogen evolution rate. EET does not limit current density once electrically conductive biofilms are formed on anodes, potentially producing 300 A/m2. Hence, IET kinetics mainly govern current density in MECs. Among parameters associated with IET kinetic, population of anode-respiring bacteria in anode biofilms, biofilm density of active microorganisms, biofilm thickness, and alkalinity are critical for current density.
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Fuentes de Energía Bioeléctrica , Electrólisis , Biopelículas , Electrodos , Fermentación , HidrógenoRESUMEN
In this study, a mesoporous SBA-15 silica catalyst was prepared and modified with encased 1% platinum (Pt) metal nanoparticles for the hydrocracking and hydroisomerization of n-heptane in a heterogeneous reaction. The textural and structural characteristics of the nanostructured silica, including both encased and non-encased nanoparticles, were measured using small-angle X-ray diffraction (XRD), nitrogen adsorption-desorption porosimetry, Brunauer-Emmett-Teller (BET) surface area analysis, Fourier-transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Catalytic testing was carried out in a plug-flow reactor under highly controlled operating conditions involving the reactant flow rate, pressure, and temperature. Gas chromatography was used to analyze the species as they left the reactor. The results demonstrated that 1% Pt/SBA-15 has a high n-heptane conversion activity (approximately 85%). Based on the results of this experimental work, there is no selectivity in the SBA-15 catalysts for isomerization products because they are inactive at the relatively low temperature that is essential for hydroisomerization. On the other hand, the SBA-15 catalysts have a considerable selectivity for products that have cracks, owing to their ability to withstand extremely high temperatures (300-400 â°C) as well as the availability of Lewis acid sites within the catalyst structure.
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Discovering the low-energy conformations of a molecule is of great interest to computational chemists, with applications in in silico materials design and drug discovery. In this paper, we propose a variable neighbourhood search heuristic for the conformational search problem. Using the structure of a molecule, neighbourhoods are chosen to allow for the efficient use of a binary quadratic optimizer for conformational search. The method is flexible with respect to the choice of molecular force field and the number of discretization levels in the search space, and can be further generalized to take advantage of higher-order binary polynomial optimizers. It is well-suited for the use of devices such as quantum annealers. After carefully defining neighbourhoods, the method easily adapts to the size and topology of these devices, allowing for seamless scaling alongside their future improvements.
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Paraoxonase 1 (PON1) is a high-density lipoprotein (HDL)-associated enzyme that by hydrolysing exogenous and endogenous substrates can provide protection against substrate induced toxicity. To investigate the extent to which PON1 provides protection against lactone induced DNA damage, DNA damage was measured in HepG2 cells using the neutral Comet assay following lactone treatment in the presence and absence of exogenous recombinant PON1 (rPON1). Low dose lactones (10 mM) caused little or no damage while high doses (100 mM) induced DNA damage in the following order of potency: α-angelica lactone > γ-butyrolactone ~ γ-hexalactone > γ-heptalactone ~ γ-octaclactone ~ γ-furanone ~ γ-valerolactone > γ-decalactone. Co-incubation of 100 mM lactone with rPON1, resulted in almost all cells showing extensive DNA damage, particularly with those lactones that decreased rPON1 activity by > 25%. In contrast, with the lactones that are poor rPON1 subtrates (γ-decalactone and γ-furanone), rPON1 did not increase DNA damage. DNA damage induced by a 1 h co-treatment with 10 mM α-angelica lactone and rPON1 was reduced when cells when incubated for a further 4 h in fresh medium suggesting break formation was due to induced DNA damage rather than apoptosis. Preincubation (1-6 h) of α-angelica lactone with rPON1 in the absence of cells, decreased cellular DNA damage by around 40% in comparison to cells treated without preincubation. These results suggest that in addition to its well-recognised detoxification effects, PON1 can increase genotoxicity potentially by hydrolysing certain lactones to reactive intermediates that increase DNA damage via the formation of DNA adducts.
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Arildialquilfosfatasa/metabolismo , Daño del ADN/efectos de los fármacos , Lactonas/toxicidad , Arildialquilfosfatasa/administración & dosificación , Ensayo Cometa , Relación Dosis-Respuesta a Droga , Células Hep G2 , Humanos , Lactonas/administración & dosificación , Factores de TiempoRESUMEN
The synthesis of a [60]fullerene-benzyne building block and its further chemical cycloaddition reaction with graphene has resulted in a new all-carbon hybrid material which has been characterized by TGA, FTIR and Raman spectroscopies, XPS as well as AFM and TEM. Based on computational studies, the formation of both [2+2] and [4+2] cycloadducts on the graphene surface is feasible.
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Zero liquid discharge is currently an objective in livestock manure management to minimize water pollution. This paper reports the start-up phase of a novel psychrophilic (20 °C) dry anaerobic digestion of dairy manure with bedding fed at 35 % total solids and an organic loading rate of 3.0 g total chemical oxygen demand kg(-1) inoculum day(-1) in anaerobic sequence batch reactors. The specific methane (CH4) yield ranged from 165.4 ± 9.8 to 213.9 ± 13.6 NL CH4 kg(-1) volatile solids (VS) with an overall average of 188 ± 17 NL CH4 kg(-1) VS during 11 successive start-up cycles (231 days) and a maximum CH4 production rate of 10.2 ± 0.6 NL CH4 kg(-1) VS day(-1). The inoculum-to-substrate (VS-based) ratio ranged from 4.06 to 4.47. Although methanogenesis proceeded fairly well the hydrolysis seemed to be the rate limiting step. It is possible start up psychrophilic dry anaerobic digestion of cow feces and wheat straw at feed TS of 35 % within 7-10 successive cycles (147-210 days).
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Novel high rate psychrophilic (20°C) anaerobic digestion (PAD) of undiluted cow feces (11.5-13.5% total solids) was demonstrated using sequence batch reactor in long-term operation with successive cycles of 21days treatment cycle length (TCL). At organic loading rates (OLR) 9.0, 10.0, 11.0 and 12.0g TCOD kg(-1) inoculum d(-1) average specific methane yield (SMY) was 154.0±11.7, 152.1±12.2, 126.0±2.8 and 116.0±6.1NL CH4 per kg of VS fed, respectively. Volatile solids removal averaged around 31.7±3.3%, 32.2±1.0%, 27.9±2.2% and 23.4±0.5%, respectively. Substrate-to-inoculum ratio (SIR; wet-mass basis) ranged between 1.17±0.06 and 1.43±0.05. Concentration of volatile fatty acids in the bioreactors during the TCL indicated that hydrolysis was the rate limiting reaction. High rate PAD of undiluted cow feces is possible at OLR (g TCOD kg(-1) inoculum d(-1)) 9.0 and 10.0 with a TCL of 21days; however, OLR of 11.0 and 12.0 are also possible but require longer TCL to maintain the SMY.
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Bacterias Anaerobias/metabolismo , Reactores Biológicos/microbiología , Heces/microbiología , Residuos Industriales/prevención & control , Eliminación de Residuos/métodos , Animales , Biodegradación Ambiental , Bovinos , Simulación por Computador , Industria Lechera/métodos , Modelos BiológicosRESUMEN
Cow manure with bedding is renewable organic biomass available around the year on dairy farms. Developing efficient and cost-effective psychrophilic dry anaerobic digestion (PDAD) processes could contribute to solving farm-related environmental, energy, and manure management problems in cold-climate regions. This study was to increase the organic loading rate (OLR), fed to a novel psychrophilic (20 °C) dry anaerobic digestion of 27% total solid dairy manure (cow feces and wheat straw) in sequence batch reactor (PDAD-SBR), by 133 to 160%. The PDAD-SBR process operated at treatment cycle length of 21 days and OLR of 7.0 and 8.0 g total chemical oxygen demand (TCOD) kg(-1) inoculum day(-1) (5.2 ± 0.1 and 5.8 ± 0.0 g volatile solids (VS) kg(-1) inoculum day(-1)) for four successive cycles (84 days) produced average specific methane yields (SMYs) of 147.1 ± 17.2 and 143.2 ± 11.7 normalized liters (NL) CH4 kg(-1) VS fed, respectively. PDAD of cow feces and wheat straw is possible with VS-based inoculum-to-substrate ratio of 1.45 at OLR of 8.0 g TCOD kg(-1) inoculum day(-1). Hydrolysis was the limiting step reaction. The VS removal averaged around 57.4 ± 0.5 and 60.5 ± 5.7% at OLR 7.0 and 8.0 g TCOD kg(-1) inoculum day(-1), respectively.
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Estiércol/análisis , Anaerobiosis , Animales , Reactores Biológicos , Bovinos , Digestión , Heces/química , Metano/análisis , Tallos de la Planta/química , Triticum/químicaRESUMEN
Zero liquid discharge is increasingly adopted as an objective for waste treatment process. The objective of this study was to increase the feed total solids (TS) and the organic loading rate (OLR) fed to a novel psychrophilic (20°C) dry anaerobic digestion (PDAD). Duplicate laboratory-scale bioreactors were fed cow feces and wheat straw (35% TS in feed) at OLR of 6.0 g TCOD kg(-1) inoculum d(-1) during long-term operation (147 days consisting of 7 successive cycles). An overall average specific methane yield (SMY) of 151.8±7.9 N L CH4 kg(-1) VS fed with an averaged volatile solids removal of 42.4±4.3% were obtained at a volatile solids-based inoculum-to-substrate ratio (ISR) of 2.13±0.2. The operation was stable as indicated by biogas and VFAs profiles and the results were reproducible in successive cycles; a maximum SMY of 163.3±5.7 N L CH4 kg(-1) VS fed was obtained. Hydrolysis was the reaction limiting step. High rate PDAD of 35% TS dairy manure is possible in sequential batch reactor within 21 days treatment cycle length.
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Heces/química , Estiércol/análisis , Eliminación de Residuos/métodos , Residuos/análisis , Anaerobiosis , Animales , Biocombustibles/análisis , Reactores Biológicos , Bovinos , Femenino , Hidrólisis , Metano/química , Triticum/químicaRESUMEN
Development of efficient processes for valorising animal wastes would be a major advancement in cold-climate regions. This paper reports the results of long term (315 days experiment) of novel psychrophilic (20°C) dry anaerobic digestion (PDAD) of cow feces and wheat straw in laboratory scale sequence batch reactor operated at increasing organic loading rate. The PDAD process fed with a mixture of feces and straw (TS of 27%) over a treatment cycle length of 21 days at organic loading rate (OLR) 4.0, 5.0 and 6.0 g TCOD kg(-1) inoculum d(-1) (of 2.9 ± 0.1, 3.7 ± 0.1, and 4.4 ± 0.1g VS kg(-1) inoculum d(-1), respectively) resulted in average specific methane yield (SMY) of 187.3 ± 18.1, 163.6 ± 39.5, 150.8 ± 32.9 N L CH4 kg(-1)VS fed, respectively. PDAD of cow feces and wheat straw is possible with VS-based inoculum-to-substrate ratio of 1.4 at OLR of 6.0 g TCOD kg(-1) inoculum d(-1). Hydrolysis was the limiting step reaction.
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Estiércol , Eliminación de Residuos/métodos , Triticum , Anaerobiosis , Animales , Biocombustibles , Bovinos , Ácidos Grasos Volátiles/metabolismo , Heces , Femenino , Hidrólisis , Metano/metabolismoRESUMEN
This paper reports experimental results which demonstrate psychrophilic dry anaerobic digestion of cow feces during long-term operation in sequence batch reactor. Cow feces (13-16% total solids) has been anaerobically digested in 12 successive cycles (252 days) at 21 days treatment cycle length (TCL) and temperature of 20 °C using psychrotrophic anaerobic mixed culture. An average specific methane yield (SMY) of 184.9 ± 24.0, 189.9 ± 27.3, and 222 ± 27.7 (N)L CH4 kg(-1) of VS fed has been achieved at an organic loading rate of 3.0, 4.0, and 5.0 g TCOD kg(-1) inoculum d(-1) and TCL of 21 days, respectively. The corresponding substrate to inoculum ratio (SIR) was 0.39 ± 0.06, 0.48 ± .02, 0.53 ± 0.05, respectively. Average methane production rate of 10 ± 1.4(N)L CH4 kg(-1) VS fed d(-1) has been obtained. The low concentration of volatile fatty acids indicated that hydrolysis was the reaction limiting step.
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Reactores Biológicos , Heces/química , Metano/metabolismo , Eliminación de Residuos/métodos , Anaerobiosis , Animales , Bovinos , Femenino , CalorRESUMEN
The main objective of this study was to obtain scientifically sound data on the bioenergy potential of dairy manures from cows fed different levels of corn dried distillers grains with solubles (DDGS). Three diets differing in corn DDGS content were formulated: 0% corn DDGS (DDGS0; control diet), 10% corn DDGS (DDGS10) and 30% corn DDGS (DDGS30). Bioenergy production was determined in psychrophilic (25 ± 1 °C) sequencing batch reactors (SBRs) fed 3 g COD L(-1)·day(-1) during a two-week feeding period followed by a two-week react period. Compared to the control diet, adding DDGS10 and DDGS30 to the dairy cow diet increased the daily amount of fat excreted in slurry by 29% and 70%, respectively. The addition of DDGS30 increased the cows' daily production of fresh feces and slurry by 15% and 11%, respectively. Furthermore, the incorporation of DDGS30 in the diet increased the daily amounts of dry matter (DM), volatile solids (VS), neutral detergent fiber (NDF), acid detergent fiber (ADF) and hemicellulose by 18%, 18%, 30%, 15% and 53%, respectively, compared to the control diet. While the addition of DDGS did not significantly affect the specific CH4 production per kg VS compared to the control diet, DDGS30 increased the per cow daily CH4 production by 14% compared to the control diet.
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Degrading antibiotics discharged in the livestock manure in a well-controlled bioprocess contributes to a more sustainable and environment-friendly livestock breeding. Although most antibiotics remain stable during manure storage, anaerobic digestion can degrade and remove them to various extents depending on the concentration and class of antibiotic, bioreactor operating conditions, type of feedstock and inoculum sources. Generally, antibiotics are degraded during composting > anaerobic digestion > manure storage > soil. Manure matrix variation influences extraction, quantification, and degradation of antibiotics, but it has not been well investigated. Fractioning of manure-laden antibiotics into liquid and solid phases and its effects on their anaerobic degradation and the contribution of abiotic (physical and chemical) versus biotic degradation mechanisms need to be quantified for various manures, antibiotics types, reactor designs and temperature of operations. More research is required to determine the kinetics of antibiotics' metabolites degradation during anaerobic digestion. Further investigations are required to assess the degradation of antibiotics during psychrophilic anaerobic digestion.