Simha Prithvi, Vasiljev Anastasija, Randall Dyllon G, Vinnerås Björn
Swedish University of Agricultural Sciences, Department of Energy and Technology, Box 7032, SE-750 07 Uppsala, Sweden.
Swedish University of Agricultural Sciences, Department of Energy and Technology, Box 7032, SE-750 07 Uppsala, Sweden.
Sci Total Environ. 2023 Jun 25;879:163053. doi: 10.1016/j.scitotenv.2023.163053. Epub 2023 Mar 24.
To feed the world without transgressing regional and planetary boundaries for nitrogen and phosphorus, one promising strategy is to return nutrients present in domestic wastewater to farmland. This study tested a novel approach for producing bio-based solid fertilisers by concentrating source-separated human urine through acidification and dehydration. Thermodynamic simulations and laboratory experiments were conducted to evaluate changes in chemistry of real fresh urine dosed and dehydrated using two different organic and inorganic acids. The results showed that an acid dose of 1.36 g HSO L, 2.86 g HPO L, 2.53 g CHO·2HO L and 5.9 g CHO L was sufficient to maintain pH ≤3.0 and prevent enzymatic ureolysis in urine during dehydration. Unlike alkaline dehydration using Ca(OH) where calcite formation limits the nutrient content of fertiliser products (e.g. <15 % nitrogen), there is greater value proposition in acid dehydration of urine, as the products contain 17.9-21.2 % nitrogen, 1.1-3.6 % phosphorus, 4.2-5.6 % potassium and 15.4-19.4 % carbon. While the treatment recovered all phosphorus, recovery of nitrogen in the solid products was 74 % (±4 %). Follow-up experiments revealed that hydrolytic breakdown of urea to ammonia, chemically or enzymatically, was not the reason for the nitrogen losses. Instead, we posit that urea breaks down to ammonium cyanate, which then reacts with amino and sulfhydryl groups of amino acids excreted in urine. Overall, the organic acids evaluated in this study are promising for decentralised urine treatment, as they are naturally present in food and therefore already excreted in human urine.
为了在不跨越氮和磷的区域及全球界限的情况下养活世界,一个有前景的策略是将生活污水中的养分返还至农田。本研究测试了一种通过酸化和脱水浓缩源分离的人类尿液来生产生物基固体肥料的新方法。进行了热力学模拟和实验室实验,以评估使用两种不同的有机和无机酸对实际新鲜尿液进行加药和脱水时的化学变化。结果表明,酸剂量为1.36 g H₂SO₄/L、2.86 g H₃PO₄/L、2.53 g C₆H₈O₇·2H₂O/L和5.9 g C₄H₆O₄/L足以在脱水过程中保持尿液pH≤3.0并防止酶促尿素分解。与使用Ca(OH)₂进行碱性脱水不同,在碱性脱水中方解石的形成会限制肥料产品的养分含量(例如氮含量<15%),尿液的酸脱水具有更大的价值主张,因为产品含有17.9 - 21.2%的氮、1.1 - 3.6%的磷、4.2 - 5.6%的钾和15.4 - 19.4%的碳。虽然该处理回收了所有的磷,但固体产品中氮的回收率为74%(±4%)。后续实验表明,尿素通过化学或酶促方式水解为氨并不是氮损失的原因。相反,我们认为尿素分解为氰酸铵,然后与尿液中排出的氨基酸的氨基和巯基反应。总体而言,本研究中评估的有机酸对于分散式尿液处理很有前景,因为它们天然存在于食物中,因此已经通过人类尿液排出。