Biogas Residue Research Articles

RETRACTED: Activities of functional enzymes involved in C, N, and P conversion and their stoichiometry during agricultural waste composting with biochar and biogas residue amendments

This experiment was carried out to explore the effects of biochar, biogas residue and their combination amendment on enzyme activities and their stoichiometry during agricultural waste composting. A comprehensive analysis of the variation in, and stoichiometric correlations between, β-glucosidase (BG), N-acetylglucosaminidase (NAG), leucine aminopeptidase (LAP), and alkaline phosphatase (AKP) were determined. The results showed that biochar, biogas residue, and their combined addition significantly increased those enzyme activities. The potential C:P and N:P acquisition activities represented by ln(BG): ln(AKP) and ln(LAP + NAG): ln(AKP), were significantly decreased with biogas residue addition. BG, NAG and LAP were significantly negatively correlated with temperature, organic matter and water-soluble carbon. Redundancy analysis also showed that moisture and water-soluble carbon were significantly related to the variations of enzyme activities. Biochar and biogas residue changed the characteristics of the composting substrate, thus affecting the activity and stoichiometry of functional enzymes involved in C, N and P cycling.

Synthesis of biogas-residue-based mesoporous carbons via one-step template-free method for organic and inorganic pollutants removal

Biogas-residue-based mesoporous carbons with high adsorption capacity have been successfully synthesized via a facile template-free and one-step approach by sodium amide activation and applied in the removal of organic and inorganic pollutants in wastewater for the first time in this study. A “waste” and widely available resource, biogas residue, was utilized as carbon precursor. Different mesoporous carbons were prepared by direct co-milling and activation at various conditions, among which largest surface area of 1278 m2/g and maximum adsorption of 556 mg/g on methylene blue were achieved, respectively. It is also verified to possess superior adsorption capacity on typical organic pollutant phenanthrene (112 mg/g) and typical inorganic pollutant N/P element (N, 113 mg/g; P, 12 mg/g). The results show that the prepared mesoporous carbons possess high and universal adsorption performance toward both organic and inorganic pollutants in wastewater. Finally, the adsorption mechanism such as the relationship between the adsorption capacities and characterization results was also discussed. The low-valued raw materials, convenient procedure, energy conservation, minimum pollution and corrosion, high adsorption capacity show feasible manufacture in industry.

The potential of green biochar generated from biogas residue as a heterogeneous persulfate activator and its non-radical degradation pathways: Adsorption and degradation of tetracycline

Advanced oxidation aided by sulfate radicals (SO4−) is an effective option for the treatment of refractory pollutants from aqueous solutions. In this work, a metal-free biochar catalyst was prepared using pyrolyzed biogas residue as the raw material. The biogas residue carbon (BRC) obtained at 800 °C showed excellent catalytic activity and adsorption capacity for the removal of tetracycline (TC) with 97.9% of removal efficiency. Such performance is accounted for by the rich pores and accelerated electron transformability conferred by its defect structure with the crucial role of pyrolysis temperature in regulating catalyst properties. The BRC-800/peroxymonosulfate (PMS) system worked predominantly through non-radical pathways with high stability/recyclability without being interfered by organic/inorganic compounds in an actual water environment. The exceelent removal performance is also supported by the kinetic reaction rate of the BRC-800/PMS system as estimated to be 0.03017 min−1. This work provides a simple and effective path for modifying biogas residue waste for versatile applications.

Antibiotic degradation dominates the removal of antibiotic resistance genes during composting

To identify the key hosts involved in horizontal gene transfer (HGT) and vertical gene transfer (VGT) of antibiotic resistance genes (ARGs) and to determine the extent to and ways in which environmental properties contribute to ARG removal, the changes in ARG profile and key hosts during biogas residue and pig manure composting were investigated using metagenomic sequencing coupled with network analysis. Composting significantly reduced the abundances of ARGs other than bacA. Seventy and 41 hosts from Firmicutes, Actinobacteria, Proteobacteria and Bacteroidetes were associated with HGT and VGT, respectively. The key environmental properties were determined using structural equation modelling. Antibiotics directly affected HGT and determined ARG removal. Temperature indirectly affected HGT, mainly by influencing the degradation of antibiotics. BacA was associated only with hosts involved in VGT, which may lead to its low removal rate. These findings specify the priority and pathway of antibiotics and temperature affecting ARG profile.

A feasible biochar derived from biogas residue and its application in the efficient adsorption of tetracycline from an aqueous solution

The recovery of carbon materials from biogas residue (BR) could efficiently promote the efficient utilization of waste and the preparation of novel materials. In this study, a green and feasible reagent of citric acid was introduced and applied in the modification of biogas residue biochar (BRC). The modified biogas residue biochar (CABRC) showed a superior adsorption ability due to its higher specific surface area (approximately 6 times that of the BRC). Additionally, the adsorption capacities of CABRC and BRC for TC were 58.25 mg/g and 20.77 mg/g, respectively, while the TC adsorption performance of CABRC was 2.8 times that of BRC. The adsorption of TC by both BRC and CABRC was primarily controlled by physical adsorption and chemical adsorption (including pore filling, hydrogen bonding, π−π DEA interaction, and electrostatic interaction). Therefore, CABRC should be considered an environmentally friendly material due to its higher adsorption performance, which could expand its application in wastewater treatment.

Insights into selective adsorption mechanism of copper and zinc ions onto biogas residue-based adsorbent: Theoretical calculation and electronegativity difference

Modified biomass-based adsorption technique has attracted much attention in heavy metal ions removal, but selective adsorption behavior and mechanism of heavy metal ions adsorption onto biosorbent still need to be further clarified. Herein, a carboxylated biogas residue (BR-COOH) was prepared to remove the Cu2+ and Zn2+ from single/binary heavy metal ions solution and explore selective adsorption mechanism. The results exhibited that the adsorption capacities of BR-COOH for Cu2+ was higher than that for Zn2+ obviously, whether in the single or binary heavy metal ions solution. Meanwhile, the introduced carboxy groups were identified as the main sites for metal ions adsorption. Density functional theory (DFT) calculation results exhibited that the adsorption energy of Cu2+ (-0.51 eV) onto BR-COOH was lower than that of Zn2+ (-0.47 eV), indicating that the Cu2+ adsorbed on BR-COOH was more stable than Zn2+. Moreover, the metal ions adsorption capacity of BR-COOH was positively correlated with their electronegativity, which was due to that the metal ions with stronger electronegativity was more easily interacted with the negatively charged oxygen in carboxyl groups. The same results were also verified in the control experiment conducted with two other biosorbents. Therefore, the work provided a new and in-depth insight into selective adsorption of metal ions onto carboxylated biosorbent.

Recovery of Nitrogen from Low-Cost Plant Feedstocks Used for Bioenergy: A Review of Availability and Process Order

The cost of feedstock is often a major barrier to commercialization for lignocellulosic biofuels. Much of the research on biofuel and biobased chemical production has focused on the carbohydrate, lignin, and lipid components of biomass. There are numerous opportunities for the use of lower-cost feedstocks if more attention were devoted to the recovery and utilization of the protein and other N-containing components. This review compiles data from the last two decades on nonedible/nonpalatable agricultural residues, deoiled seedcakes, bioethanol and biogas residues, and food wastes, with a focus on the amounts and types of N-containing components. Given the challenges of removing N-containing compounds from biofuel intermediates postconversion, a case is made for the extraction and purification of proteins (and other N-containing compounds) from low-cost lignocellulosic biomass before conversion to fuel. The goal of such processes is to avoid difficult fuel upgrading steps while enhancing the opportunities for additional biorefinery products and sustainable nitrogen cycles.

Metal-tolerant Pantoea sp. WP-5 and organic manures enhanced root exudation and phytostabilization of cadmium in the rhizosphere of maize.

This study investigated the phytoremediation potential of maize (Zea mays L.) in Cd-contaminated soil through co-inoculation of metal-tolerant plant beneficial rhizobacteria (MtPBR: Pantoea sp. strain WP-5) with organic manures (PM, poultry manure, and BGR, biogas residues). The objectives of this study were to (i) examine comparative efficiency of MtPBR, PM and BGR alone or in combined form to improve maize biomass and physiology and (ii) understand the role of organic acid production in root exudates of maize for Cd accumulation and translocation. Pantoea sp. WP-5 showed organic acid production and tolerance to high Cd concentration (1000 mg L-1), thereby inoculated to maize seeds sown in soil spiked with 75 mg Cd kg-1 soil and 500 g each of the organic manures per pot. The co-inoculation of MtPBR + BGR significantly (P<0.05) increased chlorophyll contents, root/shoot dry weight, photosynthetic rate, stomatal conductance, and relative water contents and decreased electrolyte leakage, malondialdehyde contents, ascorbate peroxidase, and catalase activity in maize over the control treatment. The co-inoculation of MtPBR + BGR produced significantly (P<0.05) higher concentrations of acetic and citric acid (52.7±0.5 and 22.8±0.08 μg g-1 root fwt, respectively) in root exudates of maize, which immobilized Cd within plant roots inferred by the positive relation (root Cd vs. organic acids; R2 = 0.80-0.92) and reduced Cd translocation to shoots inferred by the negative relation (shoot Cd vs. organic acids; R2 = 0.81-0.90). It is concluded that the application of MtPBR + BGR enhanced organic acid induced phytostabilization and accumulation of Cd in roots and restricted its translocation to shoots.

Comparative Effectiveness of Biogas Residue Acidification and Nitrification Inhibitors in Mitigating CO2 and N2O Emissions from Biogas Residue-Amended Soils

Owing to their high carbon and nitrogen contents, biogas residues may lead to higher carbon dioxide (CO2) and nitrous oxide (N2O) emissions from soils. Acidification of biogas slurry and application of nitrification inhibitors (NIs) could mitigate the emission of these gases. An incubation experiment was therefore carried out to investigate the effect of NIs, DMPP (3, 4-dimethylpyrazole phosphate), and PIADIN (active ingredients: 3.00–3.25% 1,2,4-triazole and 1.50–1.65% 3-methylpyrazole), on CO2 and N2O emissions from soils fertilized with biogas residues and acidified biogas residues. Biogas residues produced higher ammonium-nitrogen (NH4+-N) and nitrate-nitrogen (NO3−-N) concentrations in soils which resulted in higher emissions of CO2-C and N2O-N than that from acidified biogas residues. Both DMPP and PIADIN significantly decreased the emissions of CO2-C (8.1–55.8%) and N2O-N (87–98%) and maintained lower NH4+-N and NO3−-N concentrations when compared to control (without nitrification inhibitors). However, the DMPP had a higher reduction capability for CO2-C emissions than PIADIN in acidified biogas residue applied soil. In conclusion, the acidification of biogas residues and application of NIs are effect in reducing gaseous emission from biogas residue fertilized soils and thus could improve the fertilizer effectiveness of the residues.

Effect of bioaugmentation on lignocellulose degradation and antibiotic resistance genes removal during biogas residues composting

In this study, six strains belonging to Alcaligenes, Enterobacter and Bacillus were employed to enhance the composting process of biogas residues and agricultural wastes. The dynamic changes of dissolved organic matter (DOM), microbial community and functional genes in composting was monitored. It was found bioaugmentation reduced the content of lignocellulose in the compost by 27.14–66.30%, and increased the seed germination index (GI) of the compost by 37.59%. Metagenomics analysis of the composting process indicated Proteobacteria (35.38%-64.19%), Actinobacteria (11.24%-28.93%) and Bacteroidetes (3.65%-9.57%) are the dominant microorganisms during the bioaugmented composting. The abundance of genes associated with glycoside hydrolase was obviously enhanced and the antibiotic resistance genes (ARGs) was significantly reduced during the bioaugmented composting. Following nursery investigation indicated the seedling substrates composed of bioaugmented compost increased the dry weight of tomato seedlings by 1.7 times, revealing obvious large-scale application potential in the resource utilization of agricultural wastes.

Optimization of Granulation Process for Binder-Free Biochar-Based Fertilizer from Digestate and Its Slow-Release Performance

Granulation of biochar-based fertilizer is one potential method to reduce transportation costs, provide for enhanced handling, and decrease the loss of fertilizer during soil application. This study aimed to synthesize binder-free biogas residue biochar-based fertilizer (RBF) pellets and investigate their physical properties and slow-release potential. Results showed that the physical properties and forming quality of the pellets reached the best when the moisture content was 7.84%, the diameter was 7 mm, the compression speed was 49.54 mm/min, and the molding pressure was 7.5 MPa. Sustained-release kinetic analysis and characterization results identified that the RBF had excellent nitrogen (N), phosphorus (P), and potassium (K) sustained release properties. The sustained release of nutrients gradually increased with the drying temperature, and the sustained-release effect of P was the best, followed by that of N and K. Therefore, RBF pellets may be applied as a green slow-release fertilizer in agricultural production. Physical, chemical, and slow-release properties could be improved by optimizing the drying and granulation process parameters, thus providing a new idea for the combination of kitchen waste recycling and sustainable agricultural development.

Effect of different direct revegetation strategies on the mobility of heavy metals in artificial zinc smelting waste slag: Implications for phytoremediation

The establishment of vegetation cover is an important strategy to reduce wind and water erosion at metal smelting waste slag sites. However, the mobility of heavy metals in waste slag-vegetation-leachate systems after the application of revegetation strategies is still unclear. Large microcosm experiments were conducted for revegetation of waste slag for 98 d using combined amendments, i.e., phosphate rock and an organic waste coming from the anaerobic digestion of pig manure (named as biogas residue), and by single- and co-planted perennial ryegrass (Lolium perenne L.) and Trifolium repens (T. repens). The results showed that the application of biogas residue slightly increased the concentrations of Zn and Cd in the leachates; however, the establishment of plants could avoid the excessive leaching of heavy metals coming from the biogas residue. The bioavailability of Cu, Zn, and Cd slightly increased, but Pb bioavailability significantly decreased regardless of single- or co-planting patterns. Additionally, the bioavailability of Cu, Zn, and Cd in the waste slag revegetated with perennial ryegrass was lower than that in T. repens under the single-planting pattern. The change in the heavy metals bioavailability under different revegetation strategies was mainly due to the root-induced change in the pH and speciation of heavy metals in the waste slag. The application of biogas residue and phosphate rock tends to the immobilization of Pb. Heavy metals mainly accumulated in the underground parts of the two herbs, and the heavy metal contents in the underground parts of perennial ryegrass were higher than those in T. repens regardless of single- or co-planting patterns. The heavy metals accumulated in T. repens were lower than those in perennial ryegrass in the single-planting pattern. The bioaccumulation and transportation factors of the two herbs were extremely low. Thus, the two herbs are potential candidates for phytostabilization of zinc smelting waste slag sites.

Triple combination of natural microbial action, etching, and gas foaming to synthesize hierarchical porous carbon for efficient adsorption of VOCs

Fungi residue, vinasse, and biogas residue differ from general biomass waste due to natural microbial action. Microbial fermentation helps create natural channels for the permeation of activators and produces proteins for natural nitrogen doping. Inspired by these advantages on porous carbon synthesis, this study adopted dual activators of KOH and KHCO3 to synthesize porous carbon with different pore ratios for efficient adsorption of volatile organic compounds (VOCs). The fungi residue possessed the least lignin due to the most severe microbial action, contributing to the best pore structures after activation. The etching effect from potassium compounds and gas foaming from the carbonate decomposition contributed to creating hierarchical porous carbon with ultra-high surface area, ca. 1536.8–2326.5 m2/g. However, KHCO3 addition also caused nitrogen erosion, such that lower adsorption capacity was attained even with a higher surface area when the mass ratio of KOH/KHCO3 decreased from 2.5:0.5 to 2:1. The maximum adsorption capacities of chlorobenzene (CB) and benzene (PhH) reached 594.0 and 394.3 mg/g, respectively. Pore structure variations after adsorption were evaluated by freeze treatment to discover the adsorption mechanism. The surface area after CB and PhH adsorption decreased 40.3% and 34.5%, respectively. Most of the mesopores might transform into micropores due to the mono/multilayer stacking of adsorbates. The VOC adsorption kinetics were simulated by the Pseudo-first- and -second-order models and Y–N model. This paper provides a new approach for high-value biomass waste utilization after microbial action to synthesize efficient adsorbents for VOCs.

Effects of bentonite on antibiotic resistance genes in biogas slurry and residue from thermophilic and mesophilic anaerobic digestion of food waste

Anaerobic digestion (AD) processes of food waste (FW) have potential risk on environments due to the prevalence and dissemination of antibiotic resistance genes (ARGs). This study investigated the effect of bentonite on methane production and the abundance of ARGs in biogas slurry and residue during AD of FW. Results showed that methane production increased by 68.52% and 56.79% with 3 g/L and 5 g/L of bentonite in mesophilic and thermophilic digestion, respectively. Adding 5 g/L of bentonite effectively reduced the genes of ermB, ermF, tetQ, tetX, sul1, sul2 and intI1 with a range of 80.82% - 100.00% in biogas residue under mesophilic reactor. The abundance of ARGs and intI1 in biogas residue were lower than in slurry under both temperatures with 5 g/L of bentonite. Statistical analysis indicated that bentonite and temperature were main driver factors which could impact ARGs by influencing the abundance and structure of microbial communities.

Combustion ash addition promotes the production of K-enriched biochar and K release characteristics

Biogas residues (BR) and maize silage (MS) from biogas plants were mixed with biomass combustion ash (ASH) for K-enriched biochar preparation. The characteristics and nutrient contents of biochar were determined by thermo-gravimetric apparatus, Fourier-transform infrared spectroscopy, X-ray diffraction, scanning electron microscope, and chemical extraction methods, respectively. The desorption kinetics and slow release mechanism of K in biochar were evaluated after an incubation experiment for 28 days. Results showed that biochar yields were improved from 36.6% to 49.0% for BR-based biochars (BRCs) and 24.9%–38.2% for MS-based biochars (MSCs) with the addition of ASH during pyrolysis. The total potassium (TK) content of composite biochar increased to the highest TK content of 37.29 mg/g in biochar derived from MS with 20 wt% ash (MSCA20%). Furthermore, slow-available K content increased from 0.86 mg/g and 1.62 mg/g of primary biochar derived from BR and MS to 6.88 mg/g and 7.8 mg/g in composite biochar with 20 wt% ash respectively. The formation of K–Si–Al–O species involved unstable clay minerals and stable insoluble minerals during the catalytic pyrolysis improved slow release performance. The composite biochar showed a slower and continuable K+ release property in the incubation experiment, releasing less than 80% of the total available K into water in 28 days. The K+ desorption kinetics fitted the Power function well, indicating release of K+ was a complex reaction process. This lab-scale work showed that the pyrolytic composite biochar from wastes in biogas plants with combustion ash addition has the potential to be slow release fertilizer. The combined thermal conversion of solid wastes provides a sustainable strategy to simultaneously achieve the reclamation of nutrients and generation of environmental benefits via the production of biochar fertilizer.

Insights into the mechanism of hydrogen peroxide activation with biochar produced from anaerobically digested residues at different pyrolysis temperatures for the degradation of BTEXS

The disposal of large amounts of biogas residue from anaerobically digested waste is a burden on environment protection. Porous biochars (BCs) were synthesized from biogas residue at three pyrolysis temperatures (300 °C, 550 °C, and 800 °C) and used to catalyze H2O2 for the degradation of benzene, toluene, ethylbenzene, xylene isomers (ortho, para, and meta), and styrene (BTEXS) to develop a new use for biogas residues. The prepared BCs were characterized through scanning electron microscopy, Brunauer–Emmett–Teller method, Fourier transform infrared spectrometry, and X-ray photoelectron spectroscopy. Results showed that BC800/H2O2 had the highest BTEXS degradation performance over 6 h. The degradation kinetic data were most consistent with the pseudo-second-order model. The different catalytic effect of the three BCs pyrolyzed at different temperatures were attributed to the dominant active sites (C–O/C–OH/C=C/C=O groups, pyridinic N, and graphitic N) that induced the production of reactive oxygen species (ROS). ROS-quenching experiments indicated that the degradation of BTEXS by BC300/H2O2, BC550/H2O2, and BC800/H2O2 involved ∙OH, ∙O2−, and 1O2. ∙OH was the dominant ROS in BC300/H2O2 and BC550/H2O2, and 1O2 was the dominant ROS in BC800/H2O2. Our findings provided new insight into the different catalytic mechanisms for BC production at different pyrolysis temperatures and demonstrated that a porous BC catalyst with high utilization value could be prepared from biogas residue and could hold considerable potential for application in BTEXS treatment in the future.

Biochar production using biogas residue and their adsorption of ammonium nitrogen and chemical oxygen demand in wastewater

Modified biochars prepared from straw, pig manure, and chicken manure biogas residues were used to adsorb and remove ammonium nitrogen (NH4+-N) and chemical oxygen demand (COD) in wastewater. The results showed that at 400–600°C, the adsorption performance of the biogas residue biochars increased with pyrolysis temperature, reaching the maximum at 550°C. Biochar from chicken manure biogas residue exhibited strong NH4+-N (20.3%) and COD (28.1%) adsorption capacity. Through FeCl3 modification, the Fe content on the surface of the biochar increased, and the adsorption data of the modified biochar conformed well to the pseudo-second-order kinetics and Langmuir model, and the reaction was dominated by chemical adsorption. The fitting calculation revealed that the FeCl3-modified biochar from chicken manure biogas residue showed maximum NH4+-N (55.29 mg/g) and COD (186.24 mg/g) absorption capacity. These results indicated that modified biochar from biogas residue could have potential application for the treatment and recycling of biogas slurry.

Biogas residue biochar shifted bacterial community, mineralization, and molecular structure of organic carbon in a sandy loam Alfisol

ABSTRACTPyrolysis into biochar as a soil amendment has been treated as an eco‐friendly and environmentally sustainable method to recycle biogas residue (BR). However, the effect of BR biochar on soil bacterial community, mineralization, and structure of organic carbon (OC) remains unrevealed, which limits the soil application of BR biochar. This study performed a microcosm incubation experiment for a sandy soil with BR and BR‐derived biochar produced at relatively low (300°C) and high (600°C) temperature (BC300 and BC600), and explored the shift in bacterial community, mineralization, and structure of OC. Results showed that BR decreased the richness and diversity of bacterial community by 19.0%–28.0%, while BR biochar caused lower reduction (4.0%–7.0%), suggesting the potential of pyrolysis in mitigating the harmful effect of BR in bacterial community. Fourier‐transform ion cyclotron resonance mass spectrometry and 13C nuclear magnetic resonance demonstrated that BR and BR biochar shifted dissolved OC toward components with 12.0%–26.0% higher molecular weight and 18.0%–21.0% more aromatics but 10.0%–22.0% lower polarity and less protein‐, carbohydrate‐, and tannin‐like species, with the shift extent being stronger for BC600. Furthermore, BC600 increased the aromaticity of bulk OC but reduced the carbohydrate, possibly due to more Actinobacteria genera. Additionally, BR significantly elevated the amount and rate of soil carbon mineralization, while the potentially mineralizable C was the lowest in the BC600‐treated soil. These findings suggested that the pyrolysis into biochar at high temperature would be a promising way to treat BR in terms of soil bacterial community richness/diversity and carbon sequestration.

Microbial degradation in the co-composting of pig manure and biogas residue using a recyclable cement-based synthetic amendment

This research investigated a synthetic amendment to improve composting and resource recycling of pig manure and biogas residue. We further examined whether adding a synthetic amendment impacts the microbial ecosystem in the composted materials. Three mixing ratios were used to investigate composting performance: no synthetic amendment (T0), 5% synthetic amendment (T1), and 10% synthetic amendment (T2) (T1 and T2 were measured as a wet weight ratio). There were no significant differences in the fundamental characteristics between composting products in T0 and T1. The moisture content of composting material in T0, T1, and T2 significantly decreased from a baseline of approximately 65% to 35.5%, 37.3%, and 55.9%, respectively. Meanwhile, the germination index significantly increased to 111.6%, 155.6%, and 62.3%, respectively. When an optimal proportion of synthetic amendment was added, T1 showed high degree of humification, lignocellulase activities, and effective biodegradation. Firmicutes, Actinobacteria, Proteobacteria, and Bacteroidetes were the dominant bacteria, while Ascomycota and Basidiomycota were the dominant fungi in all treatment groups. Amino sugar and nucleotide sugar metabolism, glycolysis, starch, and sucrose metabolism were among the primary pathways in predicted functions. The synthetic amendment can generate a mature composting product and can be reused or recycled to conserve resources.

Biogas residues in the battle for terrestrial carbon sequestration: A comparative decomposition study in the grassland soils of the Greater Region

The recycling of biogas residues resulting from the anaerobic digestion of organic waste on agricultural land is among the means to reduce chemical fertilizer use and combat climate change. This in sacco decomposition study investigates (1) the potential of the granulated biogas residue fraction to provide nutrients and enhance soil carbon sequestration when utilized as exogenous organic matter in grassland soils, and (2) the impact of different nitrogen fertilizers on the organic matter decomposition and nutrient release processes. The experiment was conducted in two permanent grasslands of the Greater Region over one management period using rooibos tea as a comparator material. The decomposition and chemical changes of the two materials after incubation in the soil were assessed by measuring the mass loss, total carbon and nitrogen status, and fibre composition in cellulose, hemicellulose and lignin. Overall, after the incubation period, granulated biogas residue maintained up to 68% of its total mass, organic matter and total carbon; increased its content in recalcitrant organic matter by up to 45% and released 45% of its total nitrogen. Granulated biogas residue demonstrated resilience and a higher response uniformity when exposed to different nitrogen fertilizers, as opposed to the comparator material of rooibos tea. However, the magnitude of fertilizer-type effect varied, with ammonium nitrate and the combinatorial treatment of raw biogas residue mixed with urea leading to the highest organic matter loss from the bags. Our findings suggest that granulated biogas residue is a biofertilizer with the potential to supply nutrients to soil biota over time, and promote carbon sequestration in grassland soils, and thereby advance agricultural sustainability while contributing to climate change mitigation.