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铁碳微电解辅助 UASB 系统强化费托废水的厌氧降解。

Enhanced anaerobic degradation of Fischer-Tropsch wastewater by integrated UASB system with Fe-C micro-electrolysis assisted.

机构信息

State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090, China.

State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090, China.

出版信息

Chemosphere. 2016 Dec;164:14-24. doi: 10.1016/j.chemosphere.2016.08.074. Epub 2016 Aug 26.

Abstract

Coupling of the Fe-C micro-electrolysis (IC-ME) into the up-flow anaerobic sludge blanket (UASB) was developed for enhanced Fischer-Tropsch wastewater treatment. The COD removal efficiency and methane production in R with IC-ME assisted both reached up to 80.6 ± 1.7% and 1.38 ± 0.11 L/L·d that higher than those values in R with GAC addition (63.0 ± 3.4% and 0.95 ± 0.09 L/L·d) and R with ZVI addition (74.5 ± 2.8% and 1.21 ± 0.09 L/L·d) under the optimum HRT (5 d). The Fe corrosion as electron donor reduced the ORP values and stimulated the activities of hydrogenotrophic methanogens to lower H partial pressure in R and R. Additionally, Fe as by-product of iron corrosion, its presence could effectively increase the percentage of protein content in tightly bound extracellular polymeric substances (TB-EPS) to promote better bioflocculation, increasing to 90.5 mg protein/g·VSS (R) and 106.3 mg protein/g·VSS (R) while this value in R1 was simply 56.6 mg protein/g·VSS. More importantly, compared with R, the excess accumulation of propionic acid and butyric acid in system was avoided. The macroscopic galvanic cells around Fe-C micro-electrolysis carriers in R, that larger than microscopic galvanic cells in R, further accelerate to transfer the electrons from anodic Fe to cathodic carbon that enhance interspecies hydrogen transfer, making the decomposition of propionic acid and butyric acid more thermodynamically feasible, finally facilitate more methane production.

摘要

铁碳微电解(IC-ME)与上流式厌氧污泥床(UASB)耦合,用于增强费-托废水处理。带有 IC-ME 辅助的 R 中的 COD 去除效率和甲烷生成量分别达到了 80.6 ± 1.7%和 1.38 ± 0.11 L/L·d,高于 GAC 添加(63.0 ± 3.4%和 0.95 ± 0.09 L/L·d)和 ZVI 添加(74.5 ± 2.8%和 1.21 ± 0.09 L/L·d)条件下最佳 HRT(5 d)下的值。铁的腐蚀作为电子供体降低了 ORP 值,并刺激了氢营养型产甲烷菌的活性,从而降低了 R 和 R 中的 H 分压。此外,铁作为铁腐蚀的副产物,其存在可以有效地增加紧密结合的胞外聚合物物质(TB-EPS)中蛋白质含量的百分比,以促进更好的生物絮凝,增加到 90.5 mg 蛋白质/g·VSS(R)和 106.3 mg 蛋白质/g·VSS(R),而 R1 中的这一值仅为 56.6 mg 蛋白质/g·VSS。更重要的是,与 R 相比,系统中丙酸和丁酸的过度积累得以避免。R 中 Fe-C 微电解载体周围的宏观原电池,大于 R 中的微观原电池,进一步加速将电子从阳极 Fe 转移到阴极碳,从而增强种间氢转移,使丙酸和丁酸的分解在热力学上更可行,最终促进更多的甲烷生成。

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