海藻糖强化厌氧氨氧化耦合反硝化工艺处理高盐废水的脱氮除碳效能

采用SBR反应器研究海藻糖强化厌氧氨氧化耦合反硝化工艺(SAD)处理高盐水的脱氮除碳效能及其动力学特性.当海藻糖为0.25 mmol·L~(-1)时反应器具有最佳的脱氮效能,NH_4~+-N、NO_2~--N、NO_3~--N和COD均可以被完全去除,与没有添加海藻糖相比,NH_4~+-N、NO_2~--N和总氮去除率分别提高了50%、43%和46%,氨氮去除速率(ARR)和亚硝氮去除速率(NRR)分别提高了81.25%和75%.当海藻糖浓度进一步提升至0.5 mmol·L~(-1)时,NH_4~+-N去除率(ARE)仅为58.82%,出水NH_4~+-N浓度下降为33.25 mg·L~(-1).相比于Haldane模型和Aiba模型,Luong模型更适合拟合海藻糖添加条件下SAD的脱氮性能.由其得到的NRRmax、KS、Sm和n分别为0.954 kg·(m3·d)-1、0 mg·L~(-1)、184.785 mg·L~(-1)和0.718.与修正的Logistic模型和修正的Boltzman模型相比,修正的Gompertz模型得到的预测值与实验值最为贴近,修正的Gompertz模型更适合描述海藻糖添加条件下单周期内基质的降解过程.     

南亚热带森林3层次物种多度之广义泊松分布模型

生物群落中物种多度分布(species abundance distribution)呈典型的倒J形,即其中存在许多稀有种、少量常见种.物种多度分布模型研究有助于解决森林生态恢复中的物种配置等实际问题.本研究考察了一种过分散(over-dispersion,或称超分布,即方差大于均值)的离散型分布,即具有λ和α两个参数...     

中试SAD-ASBR系统处理含盐废水的启动与工艺特性

采用ASBR(530 L)接种A~2/O厌氧污泥,考察了厌氧氨氧化(ANAMMOX)的启动及其与反硝化耦合处理含盐废水的脱氮特性,并对菌群结构进行了分析.结果表明,温度35℃±1℃、反应时间为14 h,160 d可实现ANAMMOX的成功启动.稳定运行阶段,ANAMMOX与反硝化耦合(SAD)使得总氮(TN)去除率和去除负荷分别达91.1%和0.45 kg·(m~3·d)~(-1);污泥呈浅红色颗粒状,厌氧氨氧化菌为优势菌,且主要菌属为Candidatus Brocadia(10.6%).此外,采用按梯度逐步提高盐度的驯化方式,可实现SAD对高盐(Cl-浓度8 000 mg·L-1)模拟火电厂废水的高效脱氮除碳,COD和TN去除率分别达93.2%和90.0%.推测SAD中反硝化主要为NO_3~--N→N_2,部分反硝化(NO_3~--N→NO_2~--N)仅占30.3%.     

厌氧氨氧化耦合反硝化工艺的启动及微生物群落变化特征

为了解厌氧氨氧化耦合反硝化启动过程中脱氮除碳性能与微生物群落的关系,通过逐步提高进水COD浓度研究了SAD启动过程中脱氮除碳性能和微生物群落变化.结果表明,随着进水COD浓度增加,出水NH_4~+-N和NO_2--N的浓度保持稳定,平均去除率均在98%以上; TN去除率逐渐升高,第3阶段TN平均去除率为95. 6%,比厌氧氨氧化理论TN去除率高6. 8%;ΔNO_3~--N/ΔNH_4~+-N明显下降,从0. 15～0. 17逐步降至0. 03～0. 07;厌氧氨氧化脱氮贡献率逐渐下降,反硝化脱氮贡献率逐渐上升,COD去除率逐步增加.污泥活性分析表明SAD启动后污泥反硝化活性明显增加,厌氧氨氧化活性略微降低.高通量测序结果表明,反应器内微生物的优势菌门为绿弯菌门、浮霉菌门、厚壁菌门、装甲菌门和变形菌门,微生物群落特征与SAD脱氮除碳性能密切相关,与脱氮除碳有关的功能微生物主要有厌氧氨氧化菌、厌氧消化菌和反硝化菌,SAD启动后反应器内厌氧氨氧化菌丰度减少,厌氧消化菌和反硝化菌丰度明显增加.     

Insights into simultaneous anammox and denitrification system with short-term pyridine exposure: Process capability,inhibition kinetics and metabolic pathways

• Short-term effect of the pyridine exposure on the SAD process was investigated. • The SAA at 150 mg/L pyridine reduced by 56.7% of the maximum value. • Inhibition kinetics models and inhibitory parameters were indicated. • Collaboration of AnAOB, HDB and PDB promoted the SAD. • Possible metabolic pathways of nitrogen and pyridine were proposed. In-depth knowledge on the role of pyridine as a bottleneck restricting the successful application of anammox-based process treating refractory coking wastewater remains unknown. In this study, the effect of short-term pyridine addition on a simultaneous anammox and denitrification (SAD) system fed with 25–150 mg/L pyridine was explored. The short-term operation showed that the highest total nitrogen (TN) removal efficiency was achieved at 25–50 mg/L of pyridine. As the pyridine addition increased, the contribution of the anammox pathway in nitrogen removal decreased from 99.3% to 79.1%, while the denitrification capability gradually improved. The specific anammox activity (SAA) at 150 mg/L pyridine decreased by 56.7% of the maximum SAA. The modified non-competitive inhibition model indicated that the 50% inhibitory concentration (IC₅₀) of pyridine on anammox was 84.18 mg/L and the substrate inhibition constant (K_i) of pyridine for self-degradation was 135.19 mg/L according to the Haldane model. Moreover, high-throughput sequencing confirmed the abundance of Candidatus Kuenenia as the amount of anammox species decreased, while the amounts of denitrifiers and pyridine degraders significantly increased as the pyridine stress increased. Finally, the possible pathways of nitrogen bioconversion and pyridine biodegradation in the SAD system were elucidated through metagenomic analysis and gas chromatography/mass spectrometry results. The findings of this study enlarge the understanding of the removal mechanisms of complex nitrogenous pyridine-containing wastewater treated by the SAD process.