同步厌氧生物脱氮除硫工艺性能的研究

研究了同步厌氧生物脱氮除硫工艺的性能。该工艺具有很高的硫化物和硝酸盐转化潜能,稳态运行时的容积硫化物去除率和容积硝酸盐去除率分别为3.73kg/(m3.d)和0.80kg/(m3.d);能够耐受580mg/L的硫化物浓度和110mg/L的硝酸盐浓度,适宜浓度分别为280mg/L和67.5mg/L;能够耐受较高的水力负荷,适宜的水力停留时间为0.13d,反应器运行性能会因缩短水力停留时间而突发性恶化。     

实验室模拟高负荷SPAC厌氧反应器运行

采用模拟废水, 对新型高负荷螺旋式自循环(Spiral automatic circulation, SPAC)厌氧反应器的运行性能进行了实验室模拟研究。结果表明: 在30oC, 水力停留时间(HRT)为12 h, 进水COD浓度从8000 mg/L升至20 000 mg/L的条件下, 反应器的COD去除率为91.1%~95.7%, 平均去除率为93.6％。在进水浓度为20 000 mg/L, HRT由5.95 h缩短至1.57 h的工况下, COD去除率从96.0%降低至78.7%, 反应器达到最高容积负荷率306 g COD/(L·d), 最大容积COD去除率240 g/(L·d), 最高容积产气率131 L/(L·d)。该反应器对基质浓度的连续提升具有良好的适应能力。进水COD浓度由8000 mg/L提升至20 000 mg/L时, 出水COD浓度一直处在较低水平(平均为852?mg/L), 容积COD去除率和容积产气率分别提高162%和119%。该反应器对HRT的连续缩短也有良好的适应能力。HRT由5.95 h缩短至1.57 h时,反应器容积COD去除率和容积产气率分别升高191%和195%。     

生产性短程硝化-厌氧氨氧化装置处理制药废水的启动性能

为拓展新型生物脱氮技术的应用领域,研究了生产性短程硝化-厌氧氨氧化装置处理制药废水的启动性能。制药废水氨氮浓度为(430.40±55.43)mg/L时,氨氮去除率达(81.75±9.10)%,实现了短程硝化-厌氧氨氧化工艺对制药废水的生物脱氮。制药废水短程硝化系统的启动时间约为74 d,亚硝氮积累率达(52.11±9.13)%,证明了结合模拟废水和实际废水的"两步法"模式对短程硝化系统启动的适用性。制药废水厌氧氨氧化系统的启动时间约为145 d,最大容积氮去除速率达6.35 kg N/(m3·d),容积效能为传统硝化-反硝化工艺的数十倍,证明了结合菌种自繁和菌种流加的模式对厌氧氨氧化系统启动的适用性。     

中试厌氧氨氧化反应器的启动与调控

研究了中试厌氧氨氧化(Anaerobic ammonium oxidation,Anammox)反应器的启动性能。结果表明,以硝化反硝化污泥、短程硝化污泥、厌氧絮体污泥和厌氧颗粒污泥混合接种,经过255d的运行,可在常温下(5oC～27oC)成功启动中试Anammox反应器,反应器的基质氮去除速率可达1.30kg/(m3·d)。厌氧氨氧化是致碱反应,厌氧氨氧化成为反应器内的主导反应后,进水pH宜控制在厌氧氨氧化适宜范围的偏低水平(6.8左右)。亚硝酸盐既是Anammox菌的基质,也是抑制剂,控制进水亚硝酸盐浓度(13～36mg/L)有助于厌氧氨氧化反应。菌种是生物反应器的功能之源,向中试装置投加少量厌氧氨氧化污泥(投加比2%),可大大加速中试Anammox反应器的启动进程。     

ABR结合SBR法处理印染废水的研究

采用实验室规模的厌氧折流板反应器(ABR)与序批式活性污泥曝气反应器(SBR)结合工艺处理印染废水。通过对ABR-SBR处理系统工艺条件的试验,在ABR段HRT为24~36 h,污泥负荷为0.43~2.46 kg COD/(m3.d),进水pH值为6.5~8.0,温度20℃~35℃;SBR段的溶解氧为2 mg/L,曝气时间为3~10 h,沉淀时间为2 h的条件下,经处理的印染工业废水COD、色度和苯胺去除率分别为32%~95%、89%~99%和50%~98%,其COD为30.0~97.1 mg/L,色度为8~40倍,苯胺浓度为0.20~0.95mg/L,达到了国家一级排放标准。     

短程硝化启动运行中功能菌群变化研究

【目的】短程硝化-厌氧氨氧化是可实现的最短生物脱氮工艺,短程硝化是实现该工艺的重要环节和必要条件。【方法】采用序批式反应器(SBR)来实现短程硝化过程的启动和稳定运行,并对该过程中的相关功能菌群变化进行检测分析。【结果】通过控制低DO浓度(<1 mg/L)和逐步提高氨氮进水负荷,可抑制氨氧化细菌(NOB)菌群增殖并促进亚硝酸氧化菌(AOB)菌群规模显著扩大,实现短程硝化过程的启动和稳定运行。在氨氮进水负荷为0.055 kg/(m3.d)时,平均氨氮去除容积负荷和污泥负荷可达到0.043kg/(m3.d)和0.16 kg/(kg.d),平均亚硝酸盐积累率可达到83.4%。在短程硝化启动和稳定运行过程中,NOB菌群密度从2.0×105CFU/mL降至1.5×104CFU/mL,相对丰度从5.51%降至2.14%;AOB菌群密度从4.5×104CFU/mL增加至1.5×107CFU/mL,相对丰度从0.18%增加至7.25%。【结论】AOB菌群规模的扩大是实现短程硝化和氨氮去除能力提高的主要原因,同时较高的进水氨氮浓度和负荷也会造成亚硝化活性的抑制。     

厌氧氨氧化膨胀床反应器的运行性能

试验研究了以竹炭为载体的厌氧氨氧化膨胀床反应器的运行性能.接种反硝化污泥,用模拟废水可成功启动该反应器:运行至144 d时,容积总氮去除率达到3.02 kg N/m3/d.这是国内文献报道的最高水平.动力学分析表明.这种反应器的最大容积总氮去除率可迭12.77 kg N/m3/d.具有很大的脱氮潜能.反应器的启动过程可分为菌体自溶、活性延滞和活性提高三个阶段.与此相应,污泥性状也从黄褐色絮状污泥变为棕灰色颗粒污泥和红色颗粒污泥.红色颗粒污泥以杆茵和球菌为主.厌氧氨氧化活性可达0.56mg TN/(mgprotein)/h,它们是反应器厌氧氨氧化功能的主要承载者.     

Anammox反应器启动过程中颗粒污泥性状变化特性

以厌氧颗粒污泥作为接种物,通过185 d的运行,成功启动了上流式厌氧氨氧化污泥床(Upflow anaerobic sludge blanket,UASB)反应器。反应器的进水氨氮与亚硝氮浓度分别提升至224 mg/L和255 mg/L,容积氮去除速率提升至3.76 kg/(m3·d)。采用红外光谱、扫描电镜和透射电镜等对厌氧氨氧化颗粒污泥的性状进行观察,发现颗粒污泥在启动过程中经历了污泥颗粒裂解到污泥颗粒重组的过程,且厌氧氨氧化颗粒污泥表面含有丰富的官能团,说明厌氧氨氧化颗粒污泥可能具有良好的吸附性能。采用宏基因组测序的方法对启动前后颗粒污泥的生态结构进行分析,发现原接种污泥优势菌群(变形菌门、厚壁菌门、拟杆菌门)丰度大幅减少,厌氧氨氧化菌所属的浮霉状菌门丰度则由1.59%提升到23.24%。     

有机负荷对AMBR 去除高浓度废水的影响

为更好提高厌氧迁移式反应器(AMBR)的处理效能,采用自制有效容积为40.5L的5格室AMBR,通过进水COD质量浓度和水力停留时间(HRT)的调控,探讨了反应器在逐渐升高容积负荷(VLR)及突然受到高负荷冲击时对高浓度废水去除效果的影响。结果表明：VLR在3~9 kg COD×(m3·d) -1之间,COD去除率可稳定在88%以上,VLR为3.5 kg COD×(m3·d) -1时最高,达到92%,VLR超过10 kg COD×(m3·d) -1时,COD去除率开始下降,VLR超过12 kg COD×(m3·d) -1时,有机负荷超出系统承受限度,COD去除率下降到了75%。当VLR从7.5 kg COD×(m3·d) -1突然提升到15 kg COD×(m3·d) -1时,前2 d COD去除率并无明显下降,保持在84%,但在第3 d 降低到了78%,在恢复冲击前有机负荷后第4 d,COD去除率恢复到冲击前水平。     

固定载体卧式厌氧反应器处理糖蜜废水的快速启动

为高效处理高浓度有机废水而设计了固定载体卧式厌氧反应器R1和R2, 它是厌氧折流板反应器(ABR)的改进, 以活性炭纤维作为生物膜载体固定并充当反应器的折流板, 在实验室规模上对R1和R2处理糖蜜废水进行快速启动运行。HRT和ORL是影响R1和R2稳定高效运行及启动的2个重要工艺参数。实验证明: HRT为2 d时, 反应器运行最佳。在第30天时, R1的COD去除率达到84.88%, R2达到81.72%。随着进水ORL由1.25 kg/(m3·d)提升到10 kg/(m3·d), 沼气容积产气率由0.35 L/(L·d)逐渐增加到4.98 L/(L·d)。进水pH值为3.9?4.5之间, 整个启动运行过程中, 未调节pH值, R1和R2的出水pH值均在6.7?7.6之间, 2个反应器均有较强的抗酸能力, R1的pH波动更为平缓。在整个实验过程中, 污泥流失量小, 没有发生堵塞现象, 在处理酸性高浓度有机废水时, 2个反应器均表现出较强的抗负荷冲击能力。     

Combined removal of sulfur compounds and nitrate by autotrophic denitrification in bioaugmented activated sludge system

An autotrophic denitrification process using reduced sulfur compounds (thiosulfate and sulfide) as electron donor in an activated sludge system is proposed as an efficient and cost effective alternative to conventional heterotrophic denitrification for inorganic (or with low C/N ratio) wastewaters and for simultaneous removal of sulfide or thiosulfate and nitrate. A suspended culture of sulfur-utilizing denitrifying bacteria was fast and efficiently established by bio-augmentation of activated sludge with Thiobacillus denitrificans. The stoichiometry of the process and the key factors, i.e. N/S ratio, that enable combined sulfide and nitrogen removal, were determined. An optimum N/S ratio of 1 (100% nitrate removal without nitrite formation and low thiosulfate concentrations in the effluent) has been obtained during reactor operation with thiosulfate at a nitrate loading rate (NLR) of 17.18 mmol N L(-1) d(-1). Complete nitrate and sulfide removal was achieved during reactor operation with sulfide at a NLR of 7.96 mmol N L(-1) d(-1) and at N/S ratio between 0.8 and 0.9, with oxidation of sulfide to sulfate. Complete nitrate removal while working at nitrate limiting conditions could be achieved by sulfide oxidation with low amounts of oxygen present in the influent, which kept the sulfide concentration below inhibitory levels.     

Degradation of 4-chlorophenol in UASB reactor under methanogenic conditions

Treatment of simulated wastewater containing 40 mg/l of 4-chlorophenol (4-CP) was carried out in an upflow anaerobic sludge blanket (UASB) reactor under methanogenic condition. The performance of this test UASB reactor was evaluated in terms of 4-CP removal. Hydraulic retention time (HRT) and substrate:co-substrate ratio for the 4-CP removal was optimized by varying the influent flow rate (13-34.7 ml/min) and sodium acetate concentration (2-5 g/l), respectively. A control UASB reactor, which was not exposed to 4-CP was also operated under similar conditions. Organic loading rate (OLR) was varied in the range of 2-5.3 kg/m(3)/d and 1.7-4.2 kg/m(3)/d, respectively, for HRT and substrate:co-substrate ratio studies, respectively. The optimum HRT and substrate:co-substrate ratio for the removal of 4-CP was 12h and 1:75, respectively. Removal of 4-CP achieved at optimum HRT and substrate:co-substrate ratio was 88.3+/-0.7%. Removal of 4-CP occurred through dehalogenation and caused increase in chloride ion concentration in the effluent by 0.23-0.27 mg/mg 4-CP removed. The ring cleavage test showed the ortho mode of ring cleavage of 4-CP. Change in the elemental composition of the anaerobic biomass of UASB reactors was observed during the study period. Concentration of Ca(2+) increased in the biomass and this could be attributed to the biosoftening. Specific methanogenic activity of the sludge of control and test UASB reactor was 0.832 g CH(4) COD/g VSS d and 0.694 g CH(4) COD/g VSS d, respectively.     

Effects of hydraulic retention time and sulfide toxicity on ethanol and acetate oxidation in sulfate-reducing metal-precipitating fluidized-bed reactor

The effects of hydraulic retention time (HRT) and sulfide toxicity on ethanol and acetate utilization were studied in a sulfate-reducing fluidized-bed reactor (FBR) treating acidic metal-containing wastewater. The effects of HRT were determined with continuous flow FBR experiments. The percentage of ethanol oxidation was 99.9% even at a HRT of 6.5 h (loading of 2.6 g ethanol L(-1) d(-1)), while acetate accumulated in the FBR with HRTs below 12 h (loading of 1.4 g ethanol L(-1) d(-1)). Partial acetate utilization was accompanied by decreased concentrations of dissolved sulfide (DS) and alkalinity in the effluent, and eventually resulted in process failure when HRT was decreased to 6.1 h (loading of 2.7 g ethanol L(-1) d(-1)). Zinc and iron precipitation rates increased to over 600 mg L(-1) d(-1) and 300 mg L(-1) d(-1), respectively, with decreasing HRT. At HRT of 6.5 h, percent metal precipitation was over 99.9%, and effluent metal concentrations remained below 0.08 mg L(-1). Under these conditions, the alkalinity produced by substrate utilization increased the wastewater pH from 3 to 7.9-8.0. The percentage of electron flow from ethanol to sulfate reduction averaged 76 +/- 10% and was not affected by the HRT. The lowest HRT did not result in significant biomass washout from the FBR. The effect of sulfide toxicity on the sulfate-reducing culture was studied with batch kinetic experiments in the FBR. Noncompetitive inhibition model described well the sulfide inhibition of the sulfate-reducing culture. (DS) inhibition constants (K(i)) for ethanol and acetate oxidation were 248 mg S L(-1) and 356 mg S L(-1), respectively, and the corresponding K(i) values for H(2)S were 84 mg S L(-1) and 124 mg S L(-1). In conclusion, ethanol oxidation was more inhibited by sulfide toxicity than the acetate oxidation.     

Performance of anaerobic contact filter in series for treating distillery spentwash

Investigations were carried out by using rigid polyurethane foam as a packing material in the anaerobic contact filter (series) to treat distillery spentwash. The effect of hydraulic retention time (HRT) in treatment efficiency of reactor (I) and (II) was evaluated at different initial substrate concentrations ranging from 1500 mg/l to 19,000 mg/l. The effect of toxic parameters such as sulphate present in the distillery spentwash and the corresponding parameters such as total sulphide and un-ionized hydrogen sulphide generated during digestion of wastewater were evaluated to assess the reactor performance. The results showed that at 4 d HRT the overall COD removal percent ranged from 98% to 73% for an influent COD of 1500 mg/l to 19,000 mg/l. The overall performance of COD removal percent in reactor (I) and (II) at 2, 3 and 4 d HRT's were investigated. At 3 d HRT the reactor (II) showed a higher COD removal percent when compared to reactor (I), which clearly shows the role of hydraulic retention time in degradation of the organic matter present in the wastewater above an influent COD concentration of 5000 mg/l.