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      Biochar bound urea boosts plant growth and reduces nitrogen leaching

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          Abstract

          Over use of N fertilizers, most commonly as urea, had been seriously concerned as a major source of radiative N (Nr) for severe environment impacts through leaching, volatilization, and N2O emission from fertilized croplands. It had been well known that biochar could enhance N retention and use efficiency by crops in amended croplands. In this study, a granular biochar-mineral urea composite (Bio-MUC) was obtained by blending urea with green waste biochar supplemented with clay minerals of bentonite and sepiolite. This Bio-MUC material was firstly characterized by microscopic analyses with FTIR, SEM-EDS and STEM, subsequently tested for N leaching in water in column experiment and for N supply for maize in pot culture, compared to conventional urea fertilizer (UF). Microscopic analyses indicated binding of urea N to particle surfaces of biochar and clay minerals in the Bio-MUC composite. In the leaching experiment over 30 days, cumulative N release as NH4+-N and of dissolved organic carbon (DOC) was significantly smaller by >70% and by 8% from the Bio-MUC than from UF. In pot culture with maize growing for 50 days, total fresh shoot was enhanced by 14% but fresh root by 25% under Bio-MUC compared to UF. This study suggested that N in the Bio-MUC was shown slow releasing in water but maize growth promoting in soil, relative to conventional urea. Such effect could be related mainly to N retention by binding to biochar/mineral surfaces and partly by carbon bonds of urea to biochar in the Bio-MUC. Therefore, biochar from agro-wastes could be used for blending urea as combined organo/mineral urea to replace mineral urea so as to reduce N use and impacts on global Nr. Of course, how such biochar combined urea would impact N process in soil-plant systems deserve further field studies.

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          Author and article information

          Journal
          Science of The Total Environment
          Science of The Total Environment
          Elsevier BV
          00489697
          September 2019
          September 2019
          : 134424
          Article
          10.1016/j.scitotenv.2019.134424
          31726412
          fb26e4bb-defa-4063-9ad8-c733f6289624
          © 2019

          https://www.elsevier.com/tdm/userlicense/1.0/

          http://creativecommons.org/licenses/by/4.0/

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