高浓度氨氮废水同步硝化反硝化性能研究

利用序批式反应器研究了溶解氧浓度和进水碳氮比对高浓度氨氮废水脱氮性能的影响.结果表明,溶解氧浓度降低实现了短程同步硝化反硝化,并提高了反应器脱氮效率.反应器运行经历了外部碳源的摄取、PHB储存、PHB有氧氧化和同步硝化反硝化作用,PHB作为同步硝化反硝化过程中反硝化的电子供体.     

溶解氧和有机碳源对同步硝化反硝化的影响

利用SBR反应器,探讨了溶解氧(DO)和有机碳源(COD)对同步硝化好氧反硝化的影响.结果表明,DO范围在0.5～0.6 mg/L时最适合于同步硝化好氧反硝化脱氮.在同步硝化反硝化过程中出现了亚硝酸盐氮的积累,推断经由短程硝化反硝化途径.总氮的去除率随着COD/N(碳氮比)的增加而增加,当COD/N为10.05时,总氮去除率最高可达70.39%.继续增加碳氮比时,总氮去除率增加不多,并且还会导致硝化作用不完全.当存在足够的易降解有机碳源时,能发生完全的好氧反硝化作用.     

高氨氮污泥脱水液短程硝化反硝化的启动及稳定

采用A/O-CSTR工艺处理高氨氮污泥脱水液。进水氨氮浓度浓度约为375 mg/L，C/N比小于1.0，反硝化碳源明显不足。A/O反应器完成短程硝化反应，CSTR定期投加初沉污泥作为碳源进行反硝化。两者联合达到总氮去除的目的。实验研究短程硝化反应的启动过程，以及CSTR出水回流对短程硝化和系统脱氮效果的影响。实验结果表明系统具有良好的硝化反硝化效果。A/O反应器亚硝酸盐积累率迅速提高并稳定在90%以上。CSTR有效利用初沉污泥实现了稳定的反硝化。出水回流有利于提高总氮去除率，在回流比为200%时，系统平均总氮去除率达到85%以上。     

常温条件下短程硝化反硝化生物脱氮影响因素的研究

试验采用SBR工艺研究了不同盐度、NH 4-N、pH和温度等因素对含盐废水短程硝化反硝化的影响.发现在20～25 ℃,pH＞8.5条件下,通过提高进水氨氮浓度可以使亚硝化率\达到90%以上.实验证明,亚硝酸菌有较高的耐盐性,能在高盐环境中保持良好的活性.     

不同温度对SBBR同步短程硝化反硝化处理炼油催化剂废水的影响

采用SBBR在溶解氧1.0 mg/L条件下考察了不同温度对实际炼油催化剂废水脱氮系统效能的影响.结果表明,SBBR容积负荷及同步硝化反硝化(SND)三氮去除率与进水氨氮浓度正相关.不同进水浓度下,反应器SND三氮去除率最高可达40％左右.33、30及28℃条件下,反应器亚硝积累率均可稳定保持在90％以上.不同温度下短程硝化反硝化pH值及ORP变化趋势基本一致,结合在线监控pH值及ORP变化规律调控反应时间,最大限度保证短程硝化的稳定性.     

盐度对活性污泥硝化功能的影响

利用批量试验研究了盐度对常规活性污泥(非耐盐污泥)硝化功能的影响;通过逐步提高试验水的NaCl浓度驯化活性污泥,考察了驯化污泥的硝化功能;并进一步研究了适应于某NaCl浓度的耐盐硝化菌在受到盐度冲击时,其硝化功能的变化.结果表明,常规活性污泥中的硝化菌对盐度较敏感,当试验水中的NaCl质量浓度达到10.0 g/L时,污泥比硝化速率降低86%;通过逐步提高试验水的NaCl浓度对活性污泥进行长期驯化,可以驯化出耐盐硝化菌,耐盐污泥的比硝化速率接近于常规活性污泥的比硝化速率;适应于某NaCl浓度的耐盐硝化菌在受到盐度冲击时,NaCl浓度突然增加会对其产生更强的抑制作用.     

常温下连续流短程硝化反硝化研究

常温(26～30℃)下应用连续流短程硝化反硝化工艺处理模拟城市生活污水,对连续流短程硝化反硝化污泥的运行参数进行了研究.结果表明,在常温、进水NH4 -N为50 mg/L、曝气区pH为7.5～8.0、曝气量为0.3 L/min、曝气区水力停留时间为4 h的条件下,NO2- -N/(NO3- -N NO2- -N)达0.677,TN去除率为35%左右;在上述条件下,无需调节曝气区pH,选择前置反硝化区与曝气区的体积比为1:2、前置反硝化区水力停留时间为2 h、回流比为2:1时,连续流短程硝化反硝化工艺的TN去除率达88.9%,COD去除率达92.7%;pH的变化规律正确反映了系统运行状况,可作为系统运行的实时控制参数.     

实时控制SBR系统中的短程硝化反硝化

以人工模拟高氨氮废水为研究对象,采用循环间歇式曝气方式,以溶解氧浓度(DO)和pH值为过程控制参数,对SBR系统进行实时控制、全程跟踪.根据此过程中COD、NH4 -N、NO2--N和NO3--N 4项水质指标的变化情况,研究SBR系统中的短程硝化反硝化工艺.实验结果表明,在短程硝化反硝化工艺中,采用较高曝气量,并且在曝气过程中用DO和pH值作为过程控制参数是可行的.     

SBR法短程硝化处理纤维素乙醇废水的中试研究

针对纤维素产乙醇废水高有机物、高氨氮、难降解的特点,运用短程硝化反硝化脱氮工艺,基于序批式活性污泥反应器(SBR)的调试运行,研究反应器运行方式对COD去除和脱氮效能的影响,为日后纤维素乙醇废水处理的工程化提供借鉴。结果表明:通过控制DO(0.5 mg·L~(-1))、p H(7.6~8.5)和投加碳源等条件,可实现亚硝酸盐氮的积累和转化,最终三氮去除率稳定在70%以上;通过投加不同碳源对比实验,发现乙酸钠作为反硝化外加碳源比葡萄糖具有更高的效率;厌氧工艺处理过的纤维素乙醇废水经短程硝化反硝化工艺处理后,COD去除率维持在20%上下,表明废水可生化性极低,已不适应生物法处理,须利用化学氧化法才能进一步去除;通过周期实验,发现硝化阶段碱度过量对短程硝化进程影响并不明显,相反充足的碱度是保证硝化反应进行的必要条件。     

短程反硝化聚磷的反硝化特征研究

研究了温度、pH值、电子供体种类及电子受体种类对反硝化的影响.试验结果表明,(1)在相同试验条件下,亚硝酸型反硝化与硝酸型反硝化的速率与硝态氮的浓度有关.在温度为25℃、pH为7的条件下,基质浓度＜300mg/L时短程反硝化速率较快;基质浓度≥300 mg/L时,以NO3-为基质的反硝化速率较大.(2)具有大量碳源储存物(PHB)的细菌可实现快速的内源性反硝化脱氮,而处于饥饿状态的细菌的内源性反硝化效率极低.     

不同碳源下的间歇曝气反硝化实验研究

本实验研究在序批式模式下高浓度硝酸盐的反硝化,比较用甲醇、醋酸钠和消化污泥上清液作碳源。实验发现,间歇曝气有助于提高反硝化污泥的沉降性能,而厌氧条件下,污泥的沉降性能差。污泥浓度4~5gVSS/L下,3种碳源都能有效地进行反硝化。最大硝酸盐去除率为0486gNO3N/gVSS·d。开始阶段,亚硝酸盐浓度增加,但用醋酸盐和硝化污泥上清液作碳源,其浓度最终下降为零。     

碳源类型及进水量分配对CMICAO工艺脱氮除磷的影响

研究了分别以葡萄糖和乙酸钠为碳源时多点交替进水阶式A2/O(CMICAO)工艺氮磷的去除效果,以及在不同进水C/N比时各进水量分配对脱氮除磷效果的影响.结果表明,在相同的进水COD浓度下,乙酸钠比葡萄糖更适合作为碳源,更能提高脱氮除磷效率.以葡萄糖为碳源时,COD为200 mg/L、C/N比为5、缺氧池与厌氧池进水配比为1∶2时,出水COD、TN、氨氮和TP浓度分别为28.5、10.8、2.1和0.5 mg/L,均达到国家一级A排放标准.若采用葡萄糖作为碳源,投加量以使进水C/N比为5～7.5为宜,外加碳源时缺氧池与厌氧池进水分配比可统一采用1∶1.     

盐度对序批式反应器与间歇曝气膜生物反应器污水处理效果的影响

采用序批式反应器(SBR)与间歇曝气膜生物反应器(IAMBR)处理模拟生活污水,考察了进水盐度对两反应器污水处理效果的影响。研究表明,当进水盐度为0g/L(以NaCl质量浓度计,下同)时,SBR和IAMBR对总有机碳(TOC)、NH4+-N及TN的去除能力相当,IAMBR未表现出明显的优势;当进水盐度为10g/L时,SBR和IAMBR对TOC、NH4+-N及TN的去除产生明显的差异。IAMBR因为膜的截留与微生物富集作用,对污染物的去除无明显变化,依然保持了较高的污染物去除率,而SBR受盐度冲击影响较大,TOC、NH4+-N及TN的去除率均大幅降低,说明IAMBR具有较高的抗盐度冲击性能。     

反硝化除磷的影响特性试验

采用SBR反应器(厌氧/缺氧/好氧工艺),分别研究了乙酸盐及硝酸盐浓度变化对反硝化除磷的影响特性。试验结果表明,当进水COD浓度>230mg/L时,乙酸盐浓度的变化对释磷、除磷速率等影响并不显著。在硝酸盐浓度<30mg/L时,硝酸盐浓度越高,缺氧段除磷速率也就越高。在C/P>23,C/N>5条件下,SBR系统对磷、氮去除率在90%以上。     

Influences of influent carbon source on extracellular polymeric substances (EPS) and physicochemical properties of activated sludge

It is necessary to understand the bioflocculation, settling and dewatering characteristics in the activated sludge process in order to establish more efficient operational strategies. The influences of carbon source on the extracellular polymeric substances (EPS) and flocculation, settling and dewatering properties of the activated sludge were investigated. Laboratory-scale completely mixed activated sludge processes were used to grow the activated sludge with different carbon sources of starch, glucose and sodium acetate. The sludge fed with acetate had highest loosely bound EPS (LB-EPS) and that fed with starch lowest. The amount of tightly bound EPS (TB-EPS), protein content in LB-EPS, polysaccharide content and protein contents in TB-EPS, were independent of the influent carbon source. The polysaccharide content in LB-EPS of the activated sludge fed with sodium acetate was lower slightly than those of starch and glucose. The sludge also had a nearly consistent flocs size and the sludge volume index (SVI) value. ESS content of the sludge fed with sodium acetate was higher initially, although it was similar to those fed with glucose and starch finally. However, the specific resistance to filtration and normalized capillary suction time fluctuated first, but finally were stable at around 5.0 × 10⁸ m kg⁻¹ and 3.5 s L g⁻¹ SS, respectively. Only the protein content in LB-EPS weakly correlated with the flocs size and SVI of the activated sludge. But there was no correlation between any other EPS contents or components and the physicochemical properties of the activated sludge.     

Impact of carbon source on nitrous oxide emission from anoxic/oxic biological nitrogen removal process and identification of its emission sources

Wastewater treatment is an important source of nitrous oxide (N₂O), which is a strong greenhouse gas and dominate ozone-depleting substance. The purpose of this study was to evaluate the effect of carbon source on N₂O emission from anoxic/oxic biological nitrogen removal process. The mechanisms of N₂O emission were also studied. Long-term experiments were operated to evaluate the effect of three different carbon sources (i.e., glucose, sodium acetate, and soluble starch) on N₂O emission characteristics. And batch experiments, in the presence or absence of specific inhibitors, were carried out to identify the sources of N₂O emission. The ammonia-oxidizing bacteria (AOB) and denitrifiers community compositions under different circumstances were also analyzed based on which the underlying mechanisms of N₂O emission were elucidated. The conversion ratios of N₂O in reactors with glucose, sodium acetate, and soluble starch were 5.3 %, 8.8 %, and 2.8 %, respectively. The primary process responsible for N₂O emission was nitrifier denitrification by Nitrosomonas-like AOB, while denitrification by heterotrophic denitrifiers acted as the sink. Reactor with sodium acetate showed the highest N₂O emission, together with the highest nitrogen and phosphate removal ratios. Carbon source has a significant impact on N₂O emission quantity and relatively minor effect on its production mechanism.     

酸碱调控及底物浓度对木糖发酵产酸特性的影响

以木糖为碳源采用间歇培养方式,对木糖厌氧发酵产酸进行研究。考察木糖浓度和初始pH值对木糖厌氧产酸的影响。结果表明,随着木糖浓度的增加,总产酸量得到提高,但木糖利用率却呈现下降的趋势。当木糖浓度为5 g/L时,其利用率为100%,15 g/L时利用率为73.9%,此时挥发性脂肪酸(VFAs)为9.22 g/L。木糖的分批投加可有效促进产酸,尤其是促进乙酸浓度的提高。pH为5.0和6.0左右时,VFAs主要成分为乙酸和丁酸;而pH为7.0～9.0时,乙酸含量明显增高,在pH值为8.0的条件下乙酸含量占总VFAs的80.1%。在pH=8.0时经过8 d左右的发酵,VFAs浓度可达9.34 g/L。     

SBR脱氮系统污泥对磷的去除研究

为了研究缺氧(75 min)-好氧(294 min)交替运行的SBR系统中除磷的原因,采用静态实验,对比了不同碳源、水质及运行环境下对磷的去除情况。实验结果表明,该SBR脱氮系统中的好氧段磷的减少是生物去除的结果。当供给碳源为丙酸-乙酸混合物(摩尔比为2∶1)、葡萄糖、淀粉或蛋白胨时,污泥都可将磷去除,去除效率依次降低;COD/NO3--N为8.77∶1(400 mg/L∶45.6 mg/L)时除磷效果明显好于5.41∶1(400 mg/L∶73.9 mg/L)和3.57∶1(400 mg/L∶112 mg/L);进水磷浓度为8 mg/L时,COD由50 mg/L增加到400 mg/L,污泥对磷的去除效果基本一样;完全的缺氧或完全的好氧环境下,污泥对磷的去除能力逐渐丧失。     

Formation of aerobic granules in the presence of a synthetic chelating agent

This paper examines the development of aerobic granular sludge in the presence of a synthetic chelating agent, nitrilotriacetic acid (NTA), in sequencing batch reactors (SBR). The growth of seed sludge at 0.26 mM, 0.52 mM and 1.05 mM of NTA was found to be significantly lower as compared to that in the absence of NTA. Aerobic granulation was significantly enhanced in the three SBRs (R2, R3 and R4), which were fed with 0.26 mM, 0.52 mM and 1.05 mM of NTA as a co-substrate, in comparison to the acetate-alone fed SBR (R1). After 2 months of operation, the mean diameter of the biomass stabilized at 0.35 mm in R1 (acetate alone), as compared to 2.18 mm in R4 (1.05 mM NTA+acetate). NTA degradation was established in SBRs, with almost complete removal during the SBR cycle. Batch experiments also showed efficient degradation of NTA by the aerobic granules.     

Model development and application for surfactant biodegradation in an acclimatising activated sludge system

A model for the biodegradation of non-ionic surfactants in an activated sludge system during acclimatisation was developed, based on respirometric and titrimetric experimental data. The data were obtained in a sequencing batch reactor (SBR) using a non-ionic surfactant as sole carbon source and sludge previously acclimatised to a different surfactant. The model was successfully applied to successive SBR-cycles of sludge acclimatisation processes subjected to two ethoxylated surfactants. The model was validated using the corresponding total organic carbon data. The evolution of the model parameters along the acclimatisation process was examined. An acclimatisation model was developed using the evolution of two of these parameters (affinity constant and inhibition constant), supported by two independently calculated acclimatisation indicators. This acclimatisation model was then applied to determine an optimal surfactant concentration sequence to feed non-acclimatised sludge during a period of 41 days, in order to induce pre-acclimatisation to this surfactant before it replaces another one in the wastewater. The model was also useful in the economical assessment of this and alternative procedures to cope with frequent changes in activated sludge feed composition.