利用西湖淤泥进行低成本有机型基质栽培试验

以西湖淤泥为主要原料，配以砻糠灰、干鸡粪、菜籽饼等，组配低成本有机型基质，旨在合理开发利用西湖淤泥。处理Ⅰ(西湖淤泥 砻糠灰 干鸡粪)与处理Ⅱ(西湖淤泥 砻糠灰 菜籽饼)均有良好的理化性质，其孔隙度、有机质含量及N、P、K含量适宜樱桃番茄的生长。处理Ⅰ樱桃番茄早期营养生长及前期产量、总产量等方面与对照(泥炭 珍珠岩 泡沫粒)无显著性差异，果实中Vc含量显著高于对照。处理Ⅱ早期营养生长不如对照，但前期产量、总产量与对照无显著性差异，干物质、Vc含量与糖度显著高于对照。处理Ⅰ、处理Ⅱ的成本约为对照的1／2左右。     

活性炭固定床操作参数的优化

研究了操作参数对活性炭固定床处理有机废气的影响。温度升高，吸附容量下降。湿度的存在会减少活性炭对有机物的吸附容量。适当的操作气速为0.1-0.5m/s，在此范围内，气速与压降在对数坐标上呈线性关系。     

Biodegradation during contaminant transport in porous media: 4. Impact of microbial lag and bacterial cell growth

Miscible-displacement experiments were conducted to examine the impact of microbial lag and bacterial cell growth on the transport of salicylate, a model hydrocarbon compound. The impacts of these processes were examined separately, as well as jointly, to determine their relative effects on biodegradation dynamics. For each experiment, a column was packed with porous medium that was first inoculated with bacteria that contained the NAH plasmid encoding genes for the degradation of naphthalene and salicylate, and then subjected to a step input of salicylate solution. The transport behavior of salicylate was non-steady for all cases examined, and was clearly influenced by a delay (lag) in the onset of biodegradation. This microbial lag, which was consistent with the results of batch experiments, is attributed to the induction and synthesis of the enzymes required for biodegradation of salicylate. The effect of microbial lag on salicylate transport was eliminated by exposing the column to two successive pulses of salicylate, thereby allowing the cells to acclimate to the carbon source during the first pulse. Elimination of microbial lag effects allowed the impact of bacterial growth on salicylate transport to be quantified, which was accomplished by determining a cell mass balance. Conversely, the impact of microbial lag was further investigated by performing a similar double-pulse experiment under no-growth conditions. Significant cell elution was observed and quantified for all conditions/systems. The results of these experiments allowed us to differentiate the effects associated with microbial lag and growth, two coupled processes whose impacts on the biodegradation and transport of contaminants can be difficult to distinguish.     

Isotopic modelling of the significance of bacterial sulphate reduction for phenol attenuation in a contaminated aquifer

A Triassic sandstone aquifer polluted with a mixture of phenolic hydrocarbons has been investigated by means of high-resolution groundwater sampling. Samples taken at depth intervals of 1 m have revealed the presence of a diving pollutant plume with a sharply defined upper margin. Concentrations of pollutant phenols exceed 4 g/l in the plume core, rendering it sterile but towards the diluted upper margin evidence for bacterial sulphate reduction (BSR) has been obtained. Groundwaters have been analysed for both delta34S-SO4 and delta18O-SO4. Two reservoirs have been identified with distinct sulphate oxygen isotope ratios. Groundwater sulphate (delta18O-SO4 = 3-5/1000) outside the plume shows a simple linear mixing trend with an isotopically uniform pollutant sulphate reservoir (delta18O-SO4 = 10-12/1000) across the plume margin. The sulphur isotope ratios do not always obey a simple mixing relation, however, at one multilevel borehole, enrichment in 34SO4 at the plume margin is inversely correlated with sulphate concentration. This and the presence of 34S-depleted dissolved sulphide indicate that enrichment in 34SO4 is the result of bacterial sulphate reduction. Delta34S analysis of trace hydrogen sulphide within the plume yielded an isotope enrichment factor (epsilon) of -9.4/1000 for present-day bacterial sulphate reduction. This value agrees with a long-term estimate (-9.9/1000) obtained from a Rayleigh model of the sulphate reduction process. The model was also used to obtain an estimate of the pre-reduction sulphate concentration profile with depth. The difference between this and the present-day profiles then gave a mass balance for sulphate consumption. The organic carbon mineralisation that would account for this sulphate loss is shown to represent only 0.1/1000 of the phenol concentration in this region of the plume. Hence, the contribution of bacterial sulphate reduction to biodegradation has thus far been small. The highest total phenolic concentration (TPC) at which there is sulphur isotope evidence of bacterial sulphate reduction is 2000 mg/l. We suggest that above this concentration, the bactericidal properties of phenol render sulphate-reducing bacteria inactive. Dissolved sulphate trapped in the concentrated plume core will only be utilised by sulphate reducers when toxic phenols in the plume are diluted by dispersion during migration.     

利用有机基质厌氧生物产氢的试验研究

对利用有机基质厌氧生物产氢过程进行了试验研究 ,结果表明 ,污泥种类、基质种类、基质浓度和起始 p H对厌氧产氢反应有显著影响。当校河底泥在以 2 0 g COD/L的果糖为基质 ,起始 p H为 6.5时 ,产氢效果最佳 ,停滞期仅为 5 h,产气速率高达5 0 .1m L/g VSS·h,且可持续 12 h,累积产气量高达 60 4.9m L/g VSS,其中氢气含量约为 5 0 %。半连续试验的结果表明 ,若及时更换和补充基质 ,适当调节 p H,就可实现持续产氢 ,在 16h内平均产气速率可达 60 .0 m L /g VSS· h,氢气含量约为 45 %。     

汽车尾气净化催化剂涂层改性研究

汽车尾气净化催化剂的净化转化效果及其耐久性，与催化剂涂层的涂覆量以及涂层和载体的结合强度密切相关。本文研究了几种不同类型表面活性剂对浆料固体含量、涂层涂覆量以及涂层结合强度的影响。研究结果表明，不使用表面活性剂时，30％为最佳的固体含量；在使用表面活性剂的情况下，浆料的固体含量可以提高至35％。非离子型表面活性剂有助于提高催化剂涂层涂覆量，而使用离子型表面活性剂的浆料球磨过程中产生大量泡沫，无法涂覆。使用非离子型表面活性剂的催化剂涂层的结合强度最好。     

Characterization of submicron particles during autumn in Beijing, China

In this study, we performed a highly time-resolved chemical characterization of nonrefractory submicron particles(NR-PM_1) in Beijing by using an Aerodyne high-resolution time-of-flight aerosol mass spectrometer(HR-ToF-AMS). The results showed the average NR-PM_1 mass concentration to be 56.4 ± 58.0 μg/m~3, with a peak at 307.4 μg/m~3. Due to the high frequency of biomass burning in autumn, submicron particles significantly increased in organic content, which accounted for 51% of NR-PM_1 on average. Secondary inorganic aerosols(sulfate + nitrate + ammonium) accounted for 46% of NR-PM_1, of which sulfate,nitrate, and ammonium contributed 15%, 20%, and 11%, respectively. To determine the intrinsic relationships between the organic and inorganic species, we used the positive matrix factorization(PMF) model to merge the high-resolution mass spectra of the organic species and NO+and NO_2~+ions. The PMF analysis separated the mixed organic and nitrate(NO+and NO_2~+) spectra into four organic factors, including hydrocarbon-like organic aerosol(HOA), oxygenated organic aerosol(OOA), cooking organic aerosol(COA), and biomass burning organic aerosol(BBOA), as well as one nitrate inorganic aerosol(NIA) factor. COA(33%) and OOA(30%) contributed the most to the total organic aerosol(OA) mass, followed by BBOA(20%) and HOA(17%). We successfully quantified the mass concentrations of the organic and inorganic nitrates by the NO+and NO2+ions signal in the organic and NIA factors. The organic nitrate mass varied from 0.01-6.8 μg/m~3, with an average of 1.0 ±1.1 μg/m~3, and organic nitrate components accounted for 10% of the total nitrate mass in this observation.     

不同基质浓度对ANAMMOX菌短期储存的影响

在15℃±1℃条件下,将厌氧氨氧化菌混培物分别置于基质浓度为0、60、120 mg·L~(-1)添加比例为1∶1的NH+4-N和NO-2-N环境中短期(15 d)储存,探究不同基质浓度对厌氧氨氧化污泥短期保存及恢复的影响.经过短期储存后进行恢复实验,结果表明,1、2、3号反应器(分别对应0、60、120 mg·L~(-1)基质浓度中储存的厌氧氨氧化菌混培物)中的厌氧氨氧化活性分别下降41. 8%、17. 4%、33. 4.%,1、3号分别由于过度内源呼吸和高基质浓度抑制,导致活性下降较大,2号反应器由于基质浓度相对合适,避免了过度内源呼吸和高基质浓度抑制,使得菌种活性在该基质浓度下保留较好;储存期间,3个反应器内均发生内源呼吸消耗自身有机物的情况,导致EPS含量下降50. 9%、41. 7%、23. 7%和粒径下降31. 6%、16. 7%、8. 2%,表明在基质匮乏期菌体通过内源呼吸的方式维持自身的活性,较高的基质浓度可以在一定程度上延缓内源呼吸过程;在恢复期间,3个反应器分别经过15、10、7 d实现脱氮性能和厌氧氨氧化活性的恢复,表明同菌种增殖富集相比,原系统通过菌种活性增强的方式脱氮性能恢复更快.     

不同运行策略下厌氧氨氧化的脱氮性能

采用厌氧氨氧化反应器(ASBR)处理模拟生活污水,考察低基质比、降温方式及pH对系统脱氮性能的影响.结果表明,温度为30℃时,控制进水NO_2~--N浓度为(30±0.2)mg·L~(-1),基质比(NO_2~--N/NH_4~+-N)由0.9升至1.4,系统NH_4~+-N和NO_2~--N去除率均值分别从54.4%和65.3%升至95.8%和92.5%;当基质比继续升高至1.6时,NH_4~+-N去除率基本不变,而NO_2~--N去除率降至54.6%,即基质比接近理论值1.32时,其厌氧氨氧化脱氮性能较强.当反应温度一次性从30℃降低至15℃时,NH_4~+-N和NO_2~--N的去除率由97.5%和98.5%分别降至35.2%和40.1%,当采用阶梯式降温方式(30℃→25℃→20℃→15℃)时,NH_4~+-N和NO_2~--N的去除率分别由97.7%和98.6%逐渐降至52.7%和62.4%.控制NO_2~--N/NH_4~+-N为1.4,逐步升高pH由7.7至8.5时,NH_4~+-N和NO_2~--N的去除率先增大后减小,当pH为8.3时系统脱氮性能最佳.     

基质比对厌氧氨氧化脱氮性能的影响

采用厌氧氨氧化反应器(ASBR)处理模拟生活污水,在温度为30℃时,控制进水NO_2~--N浓度为(30.0±0.2)mg·L~(-1),pH为(7.2±0.2),考察了NO_2~--N/NH_4~+-N分别为0.9、1.1、1.3、1.4、1.5和1.6时,对厌氧氨氧化(ANAMMOX)脱氮效果的影响.结果表明,当NO_2~--N/NH_4~+-N为1.4时,出水NH_4~+-N、NO_2~--N及TN的浓度分别为0.8、1.5和7.7 mg·L~(-1),NH_4~+-N、NO_2~--N及TN的去除率分别高达96.2%、95.4%和85.3%,此时脱氮性能最好,与发生厌氧氨氧化时NO_2~--N/NH_4~+-N理论值1.32比较接近.