用微电极测定曝气量对SBR系统中硝化作用的影响

为了研究曝气量对硝化作用的影响,实验采用3个相同的SBR装置,分别在曝气量为4、10和16 L/h的条件下处理人工污水,并采用自制的溶解氧、NO3-、NH4+和pH微电极测定了活性污泥絮体内部微元环境中相应基质的浓度。结果表明,曝气量为4 L/h时,活性污泥絮体内存在厌氧微区,NO3--N浓度减小了,发生了反硝化作用;而曝气量为10 L/h和16 L/h时,活性污泥絮体内发生的都是硝化反应,且NH4+-N浓度的减小量、NO3--N浓度的增大量都随着曝气量的增大而增大,pH随着曝气量的增大而减小。     

A Novel Design for Anaerobic Chemical Oxygen Demand and Nitrogen Removal from Leachate in a Semiaerobic Landfill

Abstract

The removal capacity of carbon and nitrogen from an artificial leachate was evaluated by using laboratory-scale columns, and a design was proposed to remove nitrogen more efficiently from a semiaerobic landfill. Five columns (i.e., two artificial municipal waste columns under anaerobic and semiaerobic conditions, an artificial construction waste column under semiaerobic conditions, and two crushed stone columns under anaerobic and semiaerobic conditions) were used. The influent load rates of organics [g chemical oxygen demand (COD)/m³ ·day], NH₄ ⁺, NO₃ ^?, and aeration conditions for the columns were varied, and the removal capacities of the columns for COD, NH₄ ⁺-N, and NO₃ ^?-N were measured.

Among the packed column materials, crushed stone was shown to be most effective in removing COD, NH₄ ⁺-N, and NO₃ ^?-N from artificial leachate. Average removal rates of crushed column under the semiaerobic condition (column D) for COD and NH₄ ⁺-N were estimated at about 150 g COD/m³·day and 20 g COD/m³ ·day, while those of crushed column under anaerobic condition (column E) for COD and NO₃ ^?-N at about 400 and 150 g COD/m³ ·day, respectively. It also was found that denitrification and nitrification reactions in column D occurred at the same time, and the ratio of denitrification to nitrification was estimated to be about 80%. Therefore, an anaerobic structure, which could be attached to the bottom of a main pipe in a semiaerobic landfill, is suggested to remove nitrogen and organic substances more effectively.     

复合沸石滤床修复北方景观水体的实验研究

以天然矿物质沸石、细砂及煤渣取代传统滤料构建复合基质生态床，表面种植景观植物，采用下向流-上向流运行方式修复北方景观水体。分别进行静态实验及不同循环速率下的动态实验，考察对水体污染物去除过程。结果表明，2种运行方式下对水体NH⁺₄-N去除率都在85%以上，其中以1 h为循环周期的运行方式去除率达97%，较静态提高12.8%；TN去除率最高为84%；TP去除不稳定，过程缓慢。煤渣层对NH⁺₄-N的去除效果差，硝化作用不彻底与反硝化作用的加强使下层出水NH⁺₄-N 、NO^-₂-N及NO^-₃-N浓度均高于上层。提高循环速率有利于对氮的去除。     

Ammonium,Nitrate and Nitrite Nitrogen and Nitrate Reductase Enzyme Activity in Groundnut (Arachis hypogaea L.) Fields After Diazinon,Imidacloprid and Lindane Treatments

Impacts of diazinon (O,O-diethyl O-2-isopropyl-6-methylpyrimidin-4-yl phosphorothioate), imidacloprid [1-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylideneamine] and lindane (1,2,3,4,5.6-hexachlorocyclohexane) treatments on ammonium, nitrate, and nitrite nitrogen and nitrate reductase enzyme activities were determined in groundnut (Arachis hypogaea L.) field for three consecutive years (1997 to 1999). Diazinon was applied for both seed- and soil-treatments but imidacloprid and lindane were used for seed treatments only at recommended rates. Diazinon residues persisted for 60 days in both the cases. Average half-lives (t_1/2) of diazinon were found 29.3 and 34.8 days respectively in seed and soil treatments. In diazinon seed treatment, NH₄ ⁺, NO₃ ^?, and NO₂ ^? nitrogen and nitrate reductase activity were not affected. Whereas, diazinon soil treatment indicated significant increase in NH₄ ⁺-N in a 1-day sample, which continued until 90 days. Some declines in NO₃ ^?N were found from 15 to 60 days. Along with this decline, significant increases in NO₂ ^?N and nitrate reductase activity were found between 1 and 30 days. Imidacloprid and lindane persisted for 90 and 120 days with average half-lives (t_1/2) of 40.9 and 53.3 days, respectively. Within 90 days, imidacloprid residues lost by 73.17% to 82.49% while such losses for lindane residues were found 78.19% to 79.86 % within 120 days. In imidacloprid seed-treated field, stimulation of NO₃ ^?N and the decline in NH₄ ⁺NO₂ ^?-N and nitrate reductase enzyme activity were observed between 15 to 90 days. However, lindane seed treatment indicated significant increases in NH₄ ⁺-N, NO₂ ^?-N and nitrate reductase activity and some adverse effects on NO₃ ^?N between 15 and 90 days.     

固态碳源去除地下水硝酸盐的模拟实验

选取了5种研究较少的固体材料,棉花、丝瓜络、甘蔗渣、可降解餐盒、木屑作为去除地下水硝酸盐的外加碳源。在锥形瓶中进行反硝化对比实验,研究了不同固态碳源下NO3--N、NO2--N、NH4+-N及pH的变化情况,分析了NO3--N及总氮的去除率。研究结果表明,反硝化过程中pH呈升高趋势,在6.9～8.5范围内浮动。可降解餐盒和丝瓜络相对于其他的固态碳源来说,对NO3--N和总氮有较高的去除率,但丝瓜络的总氮去除率明显低于可降解餐盒。可降解餐盒的硝酸盐去除率达到98.28%,总氮去除率达到93.48%。可降解餐盒能够有效地去除地下水硝酸盐,达到以废治废的效果,是经济有效的最佳固态碳源。     

基于SIMULINK的硝化反应动力学模型的仿真

利用MATLAB/SIMULINK对序批式生物膜反应器内的氨氧化细菌与亚硝酸盐氧化菌的生化反应进行仿真预测。模型的验证结果表明,适当的选择模型中的溶解氧浓度、碱度以及温度3种参数,SIMULINK仿真动力学模型能够比较准确地对氨氧化细菌与亚硝酸氧化细菌处理生活污水的过程进行仿真和预测.NH4+-N、NO2--N和NO3--N 3种基质仿真值的绝对平均误差最大为15.88,最小为1.13;NH4+-N、NO2--N和NO3--N的Nash.Suttcliffe模拟效率系数分别为99.36%、98.64%和99.25%;此外,还对SIMULINK仿真动力学模型中的溶解氧浓度、碱度以及温度进行了灵敏度分析,结果表明,温度的灵敏度最大、溶解氧次之、碱度灵敏度相对最小。     

分段进水SBR短程生物脱氮过程中N2O产生及控制

利用SBR,控制曝气量为60 L/h,利用在线pH曲线控制曝气时间,成功实现了短程生物脱氮过程,并考察了不同进水方式下SBR运行性能及N2O产量。结果表明,分段进水能够有效降低短程生物脱氮过程中外加碳源投加量。在原水进水碳氮比较低时,采用递增进水量的进水方式,能够有效降低生物脱氮过程中NO-2积累量,从而降低系统N2O产量。1次进水、2次等量进水和2次递增进水方式下,生物脱氮过程中N2O产量分别为11.1、8.86和5.04 mg/L。硝化过程中NO-2-N的积累是导致系统N2O产生的主要原因。部分氨氧化菌(AOB)在限氧条件下以NH+4-N作为电子供体,NO-2-N作为电子受体进行反硝化,最终产物是N2O。     

Simultaneous nitrification and denitrification by Pseudomonas sp. Y-5 in a high nitrogen environment

Pseudomonas sp. Y-5, a strain with simultaneous nitrification and denitrification (SND) capacity, was isolated from the Wuhan Municipal Sewage Treatment Plant. This strain could rapidly remove high concentrations of inorganic nitrogen. Specifically, Pseudomonas sp. Y-5 removed 103 mg/L of NH₄⁺-N in 24 h without nitrate or nitrite accumulation when NH₄⁺-N was its sole nitrogen source. The NH₄⁺-N removal efficiency (RE) was 97.26%, and the average removal rate (RR) was 4.30 mg/L/h. Strain Y-5 also removed NO₃^?-N and NO₂^?-N even in aerobic conditions, with average RRs of 4.39 and 4.23 mg/L/h, respectively, and REs of up to 99.34% and 95.81% within 24 h. When cultured in SND medium (SNDM-1), strain Y-5 achieved an NH₄⁺-N RE of up to 97.80% and a total nitrogen (TN) RE of 93.01%, whereas NO₃^?-N was fully depleted in 48 h. Interestingly, high nitrite concentrations did not inhibit the nitrification capacity of Y-5 when grown in SNDM-2, the RE of NH₄⁺-N and TN reached 96.29% and 94.26%, respectively, and nitrite was consumed completely. Strain Y-5 also adapted well to high concentrations of ammonia (~401.68 mg NH₄⁺-N/L) or organic nitrogen (~315.12 mg TN/L). Our results suggested that Pseudomonas sp. Y-5 achieved efficient simultaneous nitrification and denitrification, thus demonstrating its potential applicability in the treatment of nitrogen-polluted wastewater.

     

不同滤料及挂膜方式对养殖污水处理效果的研究

实验研究了填装不同滤料的4种生物滤池在3种挂膜方式下生物功能启动的情况。结果表明,相同挂膜方式下不同生物滤池中,氨氮浓度都随着系统运行时间的延长而逐渐下降,亚硝态氮浓度先上升达到峰值后下降,但悬浮球形滤料处理污水的效果明显优于其他滤料。悬浮球形滤料下不同挂膜方式,系统稳定时间不同,自然挂膜、活性污泥挂膜、优势菌挂膜三者依次约为39、30和21 d,但采用优势菌挂膜由于生物膜容易脱落,氨氮的处理效果较差。采用活性污泥法加入悬浮球形生物滤料是处理养殖污水行之有效的方法。系统运行27 d可使氨氮的浓度降低到0.033 mg/L,系统运行33 d,亚硝态氮浓度可下降到0.045 mg/L左右。     

ANAMMOX与反硝化协同作用及氮素负荷研究

向成功启动并稳定运行630 d后的UASB生物膜反应器系统连续添加有机物,分析其对厌氧氨氧化反应脱氮效果的影响,并进行氮素浓度负荷试验.在厌氧氨氧化反应器系统中连续投加有机COD(葡萄糖),系统运行稳定,有机COD(葡萄糖)存在对系统去除氮素能力影响不大,有机COD去除率达到92.0%,仅用23 d,在同一反应器系统中成功实现了厌氧氨氧化与反硝化协同作用脱氮.氮素浓度负荷试验阶段,进水氨氮(NH 4-N)、亚硝氮(NO-2-N)以及总氮(TN)浓度负荷分别从0.063 kg/(m3·d)和0.063 kg/(m3·d)和0.126 kg/(m3·d)提升到了0.239 kg/(m3·d)、0.315 kg/(m3·d)和0.554 kg/(m3·d),相应去除率分别为84.0%、93.0%和85.0%,厌氧氨氧化工艺的UASB生物膜反应器对氮素浓度负荷仍有很大提升空间.     

Effects of high ammonium level on biomass accumulation of common duckweed Lemna minor L.

Growing common duckweed Lemna minor L. in diluted livestock wastewater is an alternative option for pollutants removal and consequently the accumulated duckweed biomass can be used for bioenergy production. However, the biomass accumulation can be inhibited by high level of ammonium (NH₄ ⁺) in non-diluted livestock wastewater and the mechanism of ammonium inhibition is not fully understood. In this study, the effect of high concentration of NH₄ ⁺ on L. minor biomass accumulation was investigated using NH₄ ⁺ as sole source of nitrogen (N). NH₄ ⁺-induced toxicity symptoms were observed when L. minor was exposed to high concentrations of ammonium nitrogen (NH₄ ⁺-N) after a 7-day cultivation. L. minor exposed to the NH₄ ⁺-N concentration of 840 mg l^?1 exhibited reduced relative growth rate, contents of carbon (C) and photosynthetic pigments, and C/N ratio. Ammonium irons were inhibitory to the synthesis of photosynthetic pigments and caused C/N imbalance in L. minor. These symptoms could further cause premature senescence of the fronds, and restrain their reproduction, growth and biomass accumulation. L. minor could grow at NH₄ ⁺-N concentrations of 7–84 mg l^?1 and the optimal NH₄ ⁺-N concentration was 28 mg l^?1.     

SBR单级自养脱氮系统氮素转化途径

利用氮素计量关系和批式实验研究了SBR系统中基于短程硝化的单级自养脱氮特性和脱氮途径。结果表明,SBR系统获得良好脱氮效果,TN最高去除负荷和去除速率分别达0.49 kg N/(m3.d)和0.20 kg N/(kg VSS.d);系统中82%的氨氮转化成气体脱除,10%的氨氮转化成硝酸盐氮。批式实验结果表明,SBR系统中的污泥同时具有厌氧氨氧化、亚硝酸盐氧化和自养反硝化活性,三者的反应速率分别为0.12 kg NH4+-N/(kg VSS.d)、0.04 kg NO2--N/(kg VSS.d)和0.03 kg NO2--N/(kg VSS.d)。综上,SBR系统中氮的脱除是短程硝化、厌氧氨氧化和反硝化共同作用的结果,产生的硝酸盐是厌氧氨氧化和硝化作用所致。     

造纸白泥和粉煤灰的添加对污泥消化液中氮磷回收的影响

污泥厌氧消化液中含有丰富的氮磷，若直接排放到环境中，将会对附近水体造成严重污染。由于消化液中Mg^2＋和Ca^2＋的含量很低，严重影响了氮磷的回收效果。把造纸白泥和粉煤灰引入到污泥厌氧消化液氮磷的回收当中，可以明显地提升消化液pH和提高PO4^3-P和NH3-N回收率。实验结果表明：当造纸白泥添加量为4g／（L·h）时，曝气12h后，pH可达10．19，此时PO4^3-P和NH3-N回收率分别达到64％和45％；而当粉煤灰添加量为4g／（L·h）时，曝气12h后，pH达到9．63，PO4^3-P和NH3-N回收率分别为46％和41％。但仅用曝气方式处理，12h后，pH值仅为8．52，PO4^3-P和NH3-N回收率分别只有20％和18％。实验结果还表明，水力停留时间（HRT）越大，pH上升速度越快，幅度越大，氮磷的回收效果就越好。     

不同因素对人工湿地基质脱氮除磷效果的影响

在人工配制的污水中投入一定量的基质,不同条件下振荡培养,评价沸石、炉渣和陶瓷滤料3种基质在不同因素影响下对氨氮(NH4+-N)和总磷(TP)的吸附能力。结果表明,不同吸附时间时,沸石对NH4+-N的吸附效果最好,陶瓷滤料对TP的吸附效果最好;进水浓度对沸石吸附NH4+-N的影响较大,其吸附量随进水浓度的增大而增大,进水浓度对炉渣和陶瓷滤料吸附NH4+-N及炉渣吸附TP影响不大;3种基质对NH4+-N和TP的吸附量均是随吸附剂量的增加而降低,要达到较好的去污效果,应根据实验结果考虑基质投入量;pH值对沸石吸附NH4+-N影响显著,pH值6～7范围内吸附效果最好,pH值8～12的碱性条件有利于基质对TP的吸附。     

生物脱氮与甲烷化耦合的EGSB-BAF工艺模拟

以活性污泥3号模型(ASM3)为平台,通过引入厌氧氨氧化和甲烷化过程、以2步硝化-反硝化取代1步硝化-反硝化过程以及区分硝酸盐和亚硝酸盐条件下的内源呼吸过程,建立了同时具有甲烷化、厌氧氨氧化和2步硝化反硝化功能的EGSB-BAF工艺模型.该模型包括5种微生物、28个生物过程,同时考虑了温度、pH值和抑制性物质对生物过程的影响.以实验室EGSB-BAF集成工艺的实验数据,结合灵敏度分析对部分模型参数进行了校核.采用校核后的模型对集成工艺EGSB段和BAF段出水的COD、NH4+-N、NO2--N和NO3--N浓度进行模拟,结果表明,EGSB段和BAF段的出水中COD、NH4+-N、NO2--N和NO3--N浓度的模拟值与实测值的误差在可接受范围内.表明模型能够描述工艺的主要生物反应过程,可以作为指导工艺研究、设计和运行优化的手段.     

Effects of operating parameters on in situ NH3 emission control during kitchen waste composting and correlation analysis of the related microbial communities

Ammonia emission during composting results in anthropogenic odor nuisance and reduces the agronomic value of the compost due to the loss of nitrogen. Adjusting the operating parameters during composting is an emerging in situ odor control technique that is cheap and highly efficient. The effects of in situ NH₃ emission control were investigated in this study by simultaneously adjusting key operating parameters (such as C/N ratio, aeration rate, and moisture content) during the composting processes (C1–C9). Results showed that the average NH₃ emission concentrations for different treatments were in the order of C1 > C4 > C2 > C5 > C3 > C6 > C7 > C8 > C9. The total content of NH₃ emission (21.02 g/kg) in C9 (C/N ratio = 35, aeration rate = 15 L/min, and moisture content = 60%) was much lower than that (65.95 g/kg) in C1 (C/N ratio = 15, aeration rate = 5 L/min, and moisture content = 60%). The nitrogen loss ratio was 27.36% for C1, while 16.15% for C9. The microbial diversity and abundance in C9 and C1 were compared using high-throughput sequencing. The relationship between NH₃ emission, operating parameters, and the related functional microbial communities was also investigated. Results revealed that Nitrosospira, Nitrosomonas, Nitrobacter, Pseudomonas, Methanosaeta, Rhodobacter, Paracoccus, and Sphingobacterium were negatively related to NH₃ emission. According to the above results, the optimal values for different operating parameters for the in situ NH₃ control during kitchen waste composting were, respectively, moisture content of 70%, C/N ratio of 35, and aeration rate of 15 L/min, with the order of effectiveness from high to low being aeration rate > C/N > moisture. This information could be used as a valuable reference for the in situ NH₃ emission control during kitchen waste composting.

     

垃圾渗滤液处理工艺运行参数优化与技术比较

垃圾渗滤液是公认的一种成分复杂且难以处理的高浓度有机废水,笔者在北京市海淀区六里屯垃圾填埋场通过2007—2010年垃圾渗滤液处理的工程实践,以COD和氨氮的去除率为指标,研究了不同的垃圾渗滤液处理工艺组合,以及不同运行参数条件下对垃圾渗滤液的处理效果。结果表明,在中温UASB和A/O的平均水力停留时间(HRT)缩短1/3的情况下,通过改进A/O段曝气方式,优化系统的pH、DO等运行参数,用MBR替代絮凝工艺,使整个组合工艺对COD的年平均去除率达到了94.3%,氨氮的去除率维持在99.5%以上,出水氨氮稳定在10 mg/L以内,而改造前的COD与氨氮的年平均去除率仅为82.2%与55.3%。与改造前的UASB+A/O+絮凝工艺组合相比,改造后的UASB+A/O+MBR工艺组合具有更高的污染物去除能力、更好的抗缓冲性和稳定性。     

Size partitioning of particulate inorganic nitrogen species between the fine and coarse mode ranges and its implication to their deposition on the surface ocean

In order to discuss the dry deposition fluxes of atmospheric fixed nitrogen species, observations of aerosol chemistry including nitrate (NO₃^?) and ammonium (NH₄⁺) were conducted at two islands, Rishiri Island and Sado Island, over the Sea of Japan. Although the atmospheric concentrations of particulate NH₄⁺–N showed higher values than those of particulate NO₃^?–N at both sites, the dry deposition fluxes of the particulate NO₃^?–N were estimated to be higher than those of the particulate NH₄⁺–N. This was caused by the difference of particle sizes between the particulate NO₃^? and NH₄⁺; NH₄⁺ was almost totally contained in fine particles (d < 2.5 μm) with smaller deposition velocity, whereas NO₃^? was mainly contained in coarse particles (d > 2.5 μm) with greater deposition velocity. Fine mode NO₃^? was strongly associated with fine mode sea-salt and mineral particles, of which higher concentrations shifted the size of particulate NO₃^? toward the fine mode range. This size shift would decrease the dry deposition flux of the fixed nitrogen species on coastal waters and accelerate atmospheric transport of them to the remote oceanic areas.     

Intercomparison of Clean Air Status and Trends Network Nitrate and Nitric Acid Measurements with Data from Other Monitoring Programs

Abstract

The U.S. Environmental Protection Agency Clean Air Status and Trends Network (CASTNET) utilizes an open-face filter pack system to measure concentrations of atmospheric sulfur and nitrogen species. Concentration data for nitrogen species measured with filter pack systems sometimes deviate from data collected by other measurement systems used to measure the same species. The nature of these differences suggests that more than one sampling mechanism or atmospheric process is involved. The study presented here examines these differences by intercomparing CASTNET data with data from other studies, examining the results from earlier intercomparison studies, and conducting a field test to investigate the effect of particle size on filter pack measurement systems. Measurements of nitrogen species from the Maryland Aerosol Research and Characterization (MARCH) monitoring site were compared with nitrogen concentrations at three nearby CASTNET sites. Results indicate that CASTNET measured higher particulate nitrate (NO₃ ^-) and lower gaseous nitric acid (HNO₃) concentrations. Comparisons of NO₃ ^- from 34 collocated CASTNET and Inter-agency Monitoring of Protected Visual Environments (IMPROVE) sites show that CASTNET NO₃ ^- measurements were typically higher than the corresponding IM PROVE values. Also, results from the Lake Michigan Air Director’s Consortium Midwest Ammonia Monitoring Project demonstrated NO₃ ^- dissociation on Teflon filters. To investigate the effect of particle size, filter pack measurement systems were operated at three CASTNET sites with and without cyclones during six 7-day measurement periods from March to August 2006. Results indicate the size-selection cyclones had a significant effect on both NO₃ ^- and HNO₃ concentrations, but little effect on sulfate (SO₄ ^2-) and ammonium (NH₄ ⁺) levels. NO₃ ^- concentrations sampled with the open-face filters were significantly higher than concentrations measured with a 2.5-μm cut point, as were HNO₃ concentrations. Although limited in spatial and temporal coverage, the field study showed that the use of an open-face filter pack may allow for the collection of coarse NO₃ ^- particles and for the reaction of HNO₃ with metals/salts on the Teflon filter.     

Hazardous Waste Reduction Initiatives and the State Of Rhode Island

A comparative analysis of forest precipitation depositions was performed using pine tree barks as biomonitoring tools and throughfall collectors in pine stands at various test sites in eastern Germany. For the elements sulfate sulfur (SO₄-S), nitrate nitrogen (NO₃-N), ammonium nitrogen (NH₄-N), calcium (Ca), and iron (Fe), regression equations with r² values between 0.81 and 0.96 were derived, enabling yearly conversion of bark loads to throughfall rates (TFRs) in pine stands (g*m^-2*year^-1).

Applying this method to a network of 53 measuring sites in Dübener Heide nature park, north of Leipzig, lead to discovering spatial patterns of TFRs for SO₄-S, NO₃-N, and NH₄-N in 1994. Differences between the TFRs of sulfur and nitrogen were traced back to different emission sources and the temporal trend related to major infrastructural changes in that region since 1990. Results suggest that the bark method will be particularly suited to identifying forest precipitation depositions of ecotoxicologically relevant airborne pollutants on regional scales.