Context: Biochar can affect the storage and forms of nitrogen; thus, it may also play a role in altering the nitrogen cycle during the fermentation process of cow dung into organic fertilizer. Objective: To elucidate the mechanism and process of nitrogen transformation during the composting of cow manure with biochar, a comparative experiment was conducted. Method: This study investigates the use of biochar as a medium to enhance nitrogen storage during the aerobic composting of cow manure. The effectiveness was verified through a rapid composting experiment. Result and Conclusions: The results demonstrated that adding 5% biochar to the compost pile increased the total nitrogen content in manure by 12%. Specifically, the pyrrolic nitrogen in the composted cow manure increased from 38% to 44%, and the carbon-nitrogen ratio improved from 35% to 37%. Analysis of surface functional groups indicated that the C=O and C=C bonds in biochar played a key role in modifying nitrogen storage. Microbial analysis showed that biochar could significantly enhance the regional competitiveness of microorganisms, such as Cellvibrio, thereby boosting the expression of functional genes involved in the nitrification process, including amoABC, hao, and nxrAB. Therefore, adding 5% biochar not only enhances nitrogen storage in organic fertilizer but also changes the microbial population structure. Significance: This study carries substantial implications for the application of Biochar in the field, as well as for the development of microbial fertilizers based on cow manure.
Lignin is a promising bio-based filler for poly(butylene adipate-co-terephthalate) (PBAT), yet its true contribution to biodegradation remains unclear—most studies rely on weight loss alone, neglecting CO2 mineralization and lignin’s antibacterial activity. Here, lignin/PBAT composites with 1 wt% (LP-1) and 3 wt% (LP-2) lignin are assessed under composting conditions using both weight loss and mineralization rate. Lignin exhibits a dual role: it promotes hydrolytic weight loss (18.3% and 28.6% for LP-1 and LP-2 at 40 days), but significantly inhibits ultimate mineralization (one-year mineralization: 65.71% for pure PBAT vs. 48.74% and 29.53% for LP-1 and LP-2). A negative initial mineralization rate suggests transient antibacterial activity from released phenolic compounds. Lignin increases crystallization temperature (48.4 → 92.6 °C) and Tg (−28.5 → 49.1 °C), with 1% loading largely preserving mechanical properties. These findings demonstrate that weight loss alone is insufficient to assess degradation; mineralization must be included. Appropriate lignin loading enables balanced performance and degradation controllability, offering new insights into lifecycle assessment of green composites.