垃圾填埋场渗滤液短程生物脱氮的长期稳定性实验研究

以实际高氨氮垃圾渗滤液为研究对象,考察了单级UASB-SBR生化系统除有机物和脱氮特性,重点研究了常、低温条件下,该生化系统生物脱氮的长期稳定性.623 d的实验结果表明,基于UASB反应器内高效的反硝化和厌氧产甲烷联合去除机制,以及SBR反应器内几乎100%的硝化和反硝化,在进水COD浓度为1 000~13 800 mg·L-1条件下,最终出水COD浓度为150~1 234 mg·L-1,在进水NH+4-N浓度为574~2 360 mg·L-1条件下,最终出水NH+4-N小于10 mg·L-1,平均去除率分别在90%和98%以上,尤其是获得了99.2%的TN去除率,出水TN小于30 mg·L-1,实现垃圾渗滤液内有机物和氮的高效、深度去除.整个实验期间,SBR反应器实现并维持了稳定的生物硝化和反硝化,成功跨越2个冬季,15℃以下共计171 d,最低温度为10.2℃.     

基于氮平衡原理对南方污水处理厂中试脱氮工艺调控策略研究

通过建立A2/O工艺中氮的物料平衡方程,预测不同进水TN条件下,如何调控污泥回流比和混合液回流比使出水氮达到国家一级A标准;然后根据预测的运行参数,调试武汉市龙王嘴污水处理厂中试模拟装置,进行工况验证.结果表明,在进水TN低于30 mg·L-1,温度高于15℃时,不需要混合液回流即可实现良好的脱氮效果;在进水TN高于30 mg·L-1,温度在10~15℃之间时,增加混合液回流和DO可以提高脱氮效果,但当温度远远低于10℃时,必须同时提高混合液回流比来保证系统出水.该方法能较好依据水质状况通过调控回流比实现较好的脱氮效果.     

苹果园土壤呼吸的变化及生物和非生物因素的影响

了解果园土壤呼吸变化及其影响因素,有利于深入理解退耕还果条件下黄土高原地区土壤碳源汇功能.在长武农田生态系统国家野外站,以盛产期果园(2000年建成)为对象,利用土壤碳通量测量系统(Li-COR,Lincoln,NE,USA)于2011、2012年监测了果树冠幅下距树干不同距离处土壤呼吸、土壤水分和温度变化,分析了土壤呼吸的时空变化及其影响因素.结果表明:①土壤呼吸速率随着距树干距离延长而降低.与2 m处相比,0.5 m处土壤累积呼吸量2011年提高20%,2012年提高31%;0.5 m和2 m处土壤呼吸的温度敏感性(Q10)2011年相应依次为1.79和1.56,2012年依次为1.79和1.38.②距树干2 m处温度和水分稍高于0.5 m处,但差异不显著(P>0.05).土壤呼吸与土壤温度均呈显著的指数关系,而与土壤水分的相关性不显著.温度变化可解释土壤呼吸的季节性变化,但并不能解释距离树干不同处的差异.③距离树干不同位置处的根系密度差异是影响果园土壤呼吸空间变化及其温度敏感性的重要生物因素;④冠幅下土壤呼吸的变异系数为23%~31%.估算果园土壤呼吸需考虑其距离树干的空间差异性.     

污泥灰渣中重金属煅烧脱除规律研究及安全性评价

污泥目前被认为是磷酸盐矿的二次资源,焚烧处理可实现污泥中磷资源的浓缩富集,但其中重金属毒性问题尚待解决.该文以污泥焚烧灰渣为研究对象,利用马弗炉进行煅烧实验,通过改变反应时间(从10 min到60 min)、温度(从900℃到1200℃)及CaCl2的添加量(以Cl计,从1.5%到8.0%)研究重金属(Pb、Zn和Cu)的去除率及在煅烧灰渣中的赋存形态.结果表明:Pb有较高的去除率,且其去除率均随温度、时间及Cl含量的升高而升高,在1200℃、Cl含量为5.0%的时候有最大值为82.4%;Zn的去除率受温度的影响较大,高温时Zn有较高的去除率,且在1100℃时有最大值为83.9%;Cu的去除率较低,而在温度为1100℃时有最大的去除率为68.2%.就煅烧灰渣中重金属的赋存形态而言,各种工况下Pb在煅烧灰渣中均以残渣态存在;Zn在煅烧灰渣中主要也是以残渣态存在;Cu在煅烧后还存在一定的酸溶态,在900℃、煅烧10min时煅烧灰渣中酸溶态可达29.2%.增加CaCl2的添加量可以促进重金属的去除,同时使煅烧底渣中的重金属更稳定.地累积指数(Igeo)评价结果显示,煅烧底渣中的这3种重金属的污染程度都降低了.     

Heterogeneous Fenton-like degradation of 4-chlorophenol using iron/ordered mesoporous carbon catalyst

Ordered mesoporous carbon supported iron catalysts(Fe/OMC) were prepared by the incipient wetness impregnation method and investigated in Fenton-like degradation of 4-chlorophenol(4CP) in this work. XRD and TEM characterization showed that the iron oxides were well dispersed on the OMC support and grew bigger with the increasing calcination temperature. The catalyst prepared with a lower calcination temperature showed higher decomposition efficiency towards 4CP and H2O2, but more metals were leached. The effect of different operational parameters such as initial pH, H2O2 dosage, and reaction temperature on the catalytic activity was evaluated. The results showed that 96.1% of 4CP and 47.4% of TOC was removed after 270 min at 30°C, initial pH of 3 and 6.6 mmol/L H2O2. 88% of 4CP removal efficiency was retained after three successive runs, indicating Fe/OMC a stable catalyst for Fenton reaction. 4CP was degraded predominately by the attack of hydroxyl radical formed on the catalyst surface and in the bulk solution due to iron leaching. Based on the degradation intermediates detected by high performance liquid chromatography, possible oxidation pathways were proposed during the 4CP degradation.     

黄土丘陵区不同有机碳背景下侵蚀坡面土壤呼吸特征

以黄土丘陵区5个不同有机碳背景的坡面S型小区(坡顶为对照区、坡中为侵蚀区、坡脚为沉积区)为研究对象,通过对土壤呼吸速率的动态观测,分析坡面不同类型区土壤呼吸特征及其与土壤温湿度、有机碳和坡位的关系.结果表明,土壤温度的变化对沉积区土壤呼吸影响较大,土壤湿度的变化对侵蚀区土壤呼吸影响较大.有机碳是影响土壤呼吸的首要因子,可解释土壤呼吸变异的54.72%;其次是土壤湿度、坡位和土壤温度,分别可解释土壤呼吸变异的18.86%、16.13%和10.29%.侵蚀对坡面土壤呼吸的影响具有明显的原位和异位效应,侵蚀导致坡面侵蚀区土壤呼吸减小了21.14%,沉积区土壤呼吸增大了21.93%.侵蚀坡面土壤碳排放的源汇效应与有机碳水平有关,当土壤有机碳含量大于6.82 g·kg-1时,坡面侵蚀趋向于碳汇过程;当有机碳含量小于3.03 g·kg-1时,坡面侵蚀趋向于碳源过程.文中模型可以较好地反映有机碳和土壤温湿度与土壤呼吸的关系.     

温度对厨余垃圾两相厌氧消化中水解和酸化过程的影响

实验考查了厨余垃圾在4个温度(25℃、37℃、40℃、50℃)条件下的水解率、挥发酸(VFA)产量和速率、乳酸产量和有机酸的组成.结果表明:温度对水解和酸化过程均有较大影响,在小于37℃范围内水解率和酸化率均随温度升高而增加,最大的VFA浓度在37℃下获得,达34.4g/L.超过37℃,酸化率下降而水解率继续增加,最大水解率在50℃下获得达82%.VFA中以甲酸和乙酸为主,并有少量丙酸和丁酸产生,同时乳酸浓度一直较高.通过实验确定了厨余垃圾水解酸化过程的最优温度条件为37℃.     

Successful Treatment of Low PAH-Contaminated Sewage Sludge in Aerobic Bioreactors (7 pp) *

Background, Aims and Scope Polycyclic Aromatic Hydrocarbons (PAHs) are known for their adverse and cumulative effects at low concentration. In particular, the PAHs accumulate in sewage sludge during wastewater treatment, and may thereafter contaminate agricultural soils by spreading sludge on land. Therefore, sludge treatment processes constitute the unique opportunity of PAH removal before their release in the environment. In this study, the ability of aerobic microorganisms to degrade light and heavy PAHs was investigated in continuous bioreactors treating trace-level PAH-contaminated sludge. Methods Several aerobic reactors were operated under continuous and perfectly mixed conditions to simulate actual aerobic sludge digesters. Three sterile control reactors were performed at 35°C, 45°C or 55°C to assess PAH abiotic losses under mesophilic and thermophilic conditions. Three biological reactors were also operated at 35°C, 45°C or 55°C. Furthermore, 250 mM methanol were added in an additional mesophilic reactor (35°C). All reactors were fed with long-term PAH-contaminated sewage sludge, and PAH removal was assessed by inlet/outlet mass balance. In this study, PAH compounds ranged from 2 to 5-unsubstituted aromatic rings, i.e. respectively from Fluorene to Indeno(123cd)pyrene. Results and Discussion Significant abiotic losses were observed for the lightest PAHs (fluorene, phenanthrene and anthracene), while biodegradation occurred for all PAHs. More than 80% of the lightest PAHs were removed. Biodegradation rates inversely correlated with the increasing molecular weight, and seemed limited by the low bioavailability of the heaviest PAHs (only 50% of removal). The enhancement of PAH bioavailability by increasing the process temperature or adding methanol was tested. A temperature increase from 35°C to 45°C and then to 55°C significantly enhanced the biodegradation of the heaviest PAHs from 50% to 80%. However, high abiotic losses were observed for all PAHs at 55°C, which was attributed to volatilization. Optimal conditions were found at 45°C considering the low abiotic losses and the high PAH biodegradation rates. Similar performances were achieved by addition of methanol in the sludge. It was concluded that increasing temperatures or addition of methanol favored PAH diffusion from solids to an aqueous compartment, and enhanced their bioavailability to PAH-degrading microorganisms. Conclusion In this study, the use of long-term acclimated aerobic ecosystems showed the high potential of aerobic microorganisms to degrade a wide range of PAHs at trace levels. However, PAH biodegradation was likely controlled by their low bioavailability. Two aerobic processes have been finally proposed to achieve efficient decontamination of sewage sludge, at 45°C or in the presence of methanol. The PAH concentrations in reactor outlet were lower than the French requirements, and allow the treated sludge to be spread on agricultural land. Recommendations and Outlook The two proposed aerobic processes used physical or chemical diffusing agents. The global ecological impact of using the latter agents for treating trace level contamination must be considered. Since methanol was completely removed during the process, no additional harm is expected after treatment. However, an increase of temperature to 45°C could drastically increase the energy demand in full-scale plants, and therefore the ecological impact of the process. Moreover, since bioavailability controls PAH biodegradation, efficiency of the processes could also be influenced by the hydraulic parameters, such as mixing and aeration rates. Further experimentations in a pilot scale are therefore recommended, as well as a final assessment of the global environmental benefit of using such aerobic processes in the bioremediation of trace level compounds. - Abbreviations (PAHs): Ant – anthracene; B(a)A – benzo(a)anthracene ; B(b)F – benzo(b)fluoranthene; B(k)F – benzo(k)fluoranthene; B(ghi)P – benzo(g,h,i)perylene; B(a)P – benzo(a)pyrene; Chrys – chrysene; DB – dibenzo(a,h)anthracene; Fluor – fluoranthene; Fluo - fluorene; Ind – indeno(1,2,3-c,d)pyrene; Phe - phenanthrene; Pyr – pyrene - * The basis of this peer-reviewed paper is a presentation at the 9th FECS Conference on 'Chemistry and Environment', 29 August to 1 September 2004, Bordeaux, France.     

三江源地区1961~2005年气温极端事件变化

利用三江源地区11个气象台站1961~2005年逐日最高气温和最低气温资料，分析了三江源地区极端高温和极端低温的变化趋势。研究表明：近45年来，白天和夜间温度极端偏高的日数明显增多，分别以26 d/10 a和44 d/10 a速度在增加;白天和夜间温度极端偏低的日数显著减缓，分别以41 d/10 a和85 d/10 a的速度显著减少;年极端低温和极端高温分别以042℃/10 a和029℃/10 a的速度增加;白天和夜间温度极端偏高的日数增加主要发生在冬季和夏季，而白天和夜间温度极端偏低的日数减少主要发生在春季和秋季，夜间温度极端偏低的日数减少趋势最为明显;长江源地区极端气温变化对区域增温的响应更为敏感。