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首页> 外文期刊>Chemical engineering journal >New insight into waste activated sludge acetogenesis triggered by coupling sulfite/ferrate oxidation with sulfate reduction-mediated syntrophic consortia
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New insight into waste activated sludge acetogenesis triggered by coupling sulfite/ferrate oxidation with sulfate reduction-mediated syntrophic consortia

机译:通过将亚硫酸盐/加氢酯氧化与硫酸盐还原介导的同步联合引发的废物活性污泥醋生成的新洞察

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摘要

Acetate (HAc) production via acetogenesis is a promising biorefinery approach for waste activated sludge (WAS); however, it is hampered by the thermodynamic constraints of the bioconversion of 3-5 carbon atom short-chain fatty acids (SCFAs). Sulfate radical (SO4 center dot-)-based advanced oxidation is regarded as an appropriate candidate for accelerating WAS fermentation. In this study, we enriched an incomplete-oxidative sulfate reducing bacteria (io-SRB), combined with SO4 center dot- oxidation (generated by potassium ferrate (PF) and sodium sulfite (Na2SO3)), to boost WAS acetogenesis. Generated sulfate during SO4 center dot- oxidation served as the necessary substrates for io-SRB metabolism. A proof-of-concept based on experimental data for the whole process is presented. Results confirmed that the PF + Na2SO3 + SRB test achieved the maximum SCFAs generation (4261 +/- 210 mg COD/L with 60.9 +/- 0.5% HAc) over the PF + Na2SO3 test without io-SRB mediation (2521 +/- 109 mg COD/L with 50.6 +/- 0.3% HAc). Particle size analysis and fluorescence spectroscopy indicated that PF + Na2SO3 oxidation had positive effects on accelerating soluble organics release. SO4 center dot- was the key radical, playing the most important role, as indicated by electron paramagnetic resonance and radical scavenging analysis. X-ray photoelectron spectroscopy revealed that io-SRB mediation further promoted the transformation of polysaccharides and proteins into carboxylic acids, based on SO4 center dot- oxidation. Moreover, 79% Fe(VI) was reduced to Fe(III), and most S(IV) was converted to SO42-, approximately 40% of which was metabolized by io-SRB consortium. Clearly, SO4 center dot- oxidation and io-SRB stimulation significantly altered the composition of the key microbiome, with fermentative acidogenic bacteria predominating. The possible synergistic relationships among io-SRB, hydrolyzing bacteria and acidogens were revealed by molecular ecological network analysis. This study provides new insights into the improvement of value-added bio-metabolite recovery from SO4 center dot--based WAS fermentation.
机译:醋酸乙酸酯(HAC)通过乙酸化产生是一种有前途的废物活性污泥的生物填料方法;然而,它受到3-5个碳原子短链脂肪酸(SCFA)的生物转化的热力学约束的阻碍。基于硫酸盐的自由基(SO4中心DOT - )的晚期氧化被认为是加速的适当候选者是发酵。在该研究中,我们富集了不完全氧化的硫酸盐还原细菌(IO-SRB),与SO4中心点氧化(由叔丙酯(PF)和亚硫酸钠(Na 2 SO 3))组合,以提高乙酰化。在SO4中心点氧化期间产生的硫酸盐作为IO-SRB代谢的必要基材。提出了一种基于整个过程的实验数据的概念。结果证实,PF + Na2SO3 + SRB检验在没有IO-SRB调解的情况下通过PF + Na2SO3测试实现了最大SCFA生成(4061 +/- 0.5%HAC)(2521 +/- 109 mg COD / L为50.6 +/- 0.3%HAC)。粒度分析和荧光光谱表明,PF + Na 2 SO 3氧化对加速可溶性有机物释放具有积极作用。 SO4中心点 - 是关键的激进,播放最重要的作用,如电子顺磁共振和激进清除分析所示。 X射线光电子能谱显示,基于SO4中心点氧化,IO-SRB调解进一步促进多糖和蛋白质转化为羧酸。此外,将79%Fe(VI)还原为Fe(III),大多数S(IV)转化为SO42-,其中约40%由IO-SRB联盟代谢。清楚地,SO4中心点氧化和IO-SRB刺激显着改变了关键微生物组的组成,发酵酸性细菌优势。通过分子生态网络分析揭示了IO-SRB,水解细菌和酸性的可能协同关系。本研究提供了新的见解,进入从SO4中心点的增值生物代谢物回收的改善是发酵。

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