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    庆大霉素菌渣共厌氧沼渣微波水热炭化特性研究

    Microwave-Assisted Hydrothermal Carbonization Characteristics of Digestate from Gentamicin Residue Co-Anaerobic Digestion

    • 摘要: 抗生素菌渣厌氧发酵沼渣因残留抗生素、抗性基因(ARGs)及未降解有机污染物的持久累积,面临着严峻的环境风险与资源化瓶颈。为消除生物毒害并促进高值化资源回收,本研究构建了微波辅助水热炭化(HTC)技术方案,对比评估了庆大霉素菌渣(GBR)单发酵沼渣与GBR/玉米秸秆(CS)共发酵沼渣的处置效果,系统阐明了水热炭理化演变、孔隙结构构建、ARGs削减及氮元素留存规律。分析表明,共发酵显著促进了易降解纤维组分的转化,但沼渣中仍残留约50%(质量分数)的木质纤维素,蕴含较大的炭化与能量回收潜力。经微波水热炭化处理后,产物挥发分有效降低,固定碳及芳香化程度大幅提升。在160 ℃、90 min条件下,共发酵水热炭的高位发热量达17.13 MJ/kg,能量回收率高达88.22%;相比单发酵产物,其展现出更发达的比表面积、孔隙结构及更丰富的表面含氧官能团,显著增强了吸附应用潜力。此外,在180 ℃、120 min的微波水热条件下实现了目标ARGs高达98.40%的彻底削减;同时,氮主要以稳定有机氮形式留存,最大留存量为23.58 mg/g。综上所述,共厌氧发酵−微波水热炭化联用技术构筑了兼具危废无害化、固碳及保氮的综合调控框架,为工业危险生物质废物高值转化为多功能炭基材料提供了创新技术与理论支撑。

       

      Abstract: Anaerobic digestate derived from antibiotic-producing bacterial residues poses severe environmental risks due to the persistent accumulation of residual antibiotics, antibiotic resistance genes (ARGs), and undegraded organic contaminants. To address these hazards while promoting high-value resource recovery, this study developed a microwave-assisted hydrothermal carbonization (HTC) process to treat digestates obtained from both the single anaerobic digestion of gentamicin-producing bacterial residues (GBR) and the co-anaerobic digestion of GBR with corn stover (CS). The physicochemical properties, structural characteristics, ARG elimination, and nitrogen retention behavior of the resulting hydrochars were systematically investigated. Initial composition analysis revealed that co-anaerobic digestion effectively enhanced the degradation of cellulose and hemicellulose. However, approximately 50 wt% of lignocellulose remained in the digestate, highlighting substantial potential for downstream carbonization and energetic conversion. Following microwave-assisted HTC, the hydrochars exhibited significantly decreased volatile matter, increased fixed carbon content, and elevated degrees of aromatization and carbonization. Under optimal reaction conditions of 160 °C for 90 min, the hydrochar produced from the co-fermented digestate achieved a higher heating value of 17.13 MJ/kg with a high energy yield of 88.22%. Compared with hydrochars from the single-digestate treatment, the co-fermented hydrochar possessed a superior specific surface area, an expanded total pore volume, and a higher abundance of oxygen-containing surface functional groups, thereby enhancing its potential as an effective adsorbent. Furthermore, microwave-assisted HTC demonstrated remarkable performance in biological risk mitigation, achieving a 98.40% total reduction rate in target ARGs at 180 °C for 120 min. Meanwhile, nitrogen in the hydrochar remained predominantly in organic forms, with a maximum total nitrogen retention of 23.58 mg/g recorded at 160 °C for 90 min. Overall, coupling co-anaerobic digestion with microwave-assisted HTC provides an effective integrated framework for simultaneously detoxifying hazardous antibiotic residues, sequestering carbon, and conserving valuable nutrient nitrogen. This work offers an innovative technology and theoretical basis for transforming hazardous industrial biowastes into multi-functional hydrochar materials suitable for solid fuel, environmental remediation, and sustainable agricultural soil amendment.

       

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