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摘要
在上流式反应器中添加尼龙填料,并以小颗粒单质硫和NaHCO3作为底物构建自养高效脱氮系统。在(35±1)℃下,经过70 d运行,在HRT为2.4 h、进水NO3--N浓度为150 mg/L时,达到1.3 kg/(m3·d)的最大稳定脱氮能力。启动初期,应该缓慢提高进水NO3--N负荷来驯化反应器。S/N(摩尔)批次试验发现,在最佳摩尔比为10时,NO3--N的转化率为90%;而摩尔比低于10时,NO3--N转化速率随着单质硫粉浓度增大而增大,且摩尔比为1.1时,会出现NO2--N积累。由于传质效率低和单质硫流失问题,连续流反应器中S/N(摩尔)比宜在5.5以上,防止出现NO2--N积累。当进水NO3--N浓度为150 mg/L、HRT为2.4 h时,控制温度从(35±1)℃缓慢降至(20±0.5)℃,反应器脱氮能力稳定在1.4~1.5 kg/(m3·d),说明本反应器对温度下降适应性较强,具备常温下高效运行的能力。
Abstract
A high efficient autotrophic nitrogen-removing system is developed by adding nylon filler in an upflow reactor and using fine elemental sulfur particles and NaHCO3 as substrates.The maximum stable nitrogen removal capacity 1.3 kg/(m3·d) is achieved after 70 days' operation with an influent NO3--N concentration of 150 mg·L-1 and a HRT of 2.4 h at 35±1℃.At the beginning of the startup,the volumetric loading rate of NO3--N in influent shall be increased slowly in order to acclimate the reactor.It is found from the S/N (mol) batch experiments that the conversion rate of NO3--N can reach 90% under the optimum S/N molar ratio of 10.When the molar ratio of S/N is lower than 10,the conversion rate of NO3--N increases with the increase of the concentration of elemental sulfur.The NO2--N accumulation occurs when the molar ratio of S/N is 1.1.Due to the problems of low mass transfer efficiency and elemental sulfur loss,it is necessary to ensure S/N molar ratio above 5.5 in the continuous reactor to prevent the occurrence of NO2--N accumulation.The nitrogen removal rate of the reactor can remain stable at 1.4-1.5 kg/(m3·d) when the NO3--N concentration in influent is 150 mg·L-1,HRT is 2.4 h,the temperature decreases slowly from 35±1℃ to 20±0.5℃.It reveals that the reactor has strong adaptability to temperature drop and has the ability to run efficiently at normal temperature.
关键词
单质硫
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温度影响
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S/N(摩尔)比
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生物膜反应器
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自养反硝化
Key words
elemental sulfur
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influence of temperature
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S/N (mol) ratio
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biofilm reactor
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autotrophic denitrification
Author summay
新型单质硫自养生物膜反应器脱氮性能研究[J].
现代化工, 2018, 38(5): 181-186 DOI:10.16606/j.cnki.issn0253-4320.2018.05.041