采用高效菌提高普通活性污泥系统抗2,4-DCP负荷冲击能力

研究了用于处理生活污水的普通活性污泥反应器(CAS)受到2,4-二氯酚(2,4-DCP)间歇性负荷冲击时,投加高效菌的生物强化系统和对照系统对污染物的响应及系统稳定性,并考察了长期运行过程中强化系统对目标污染物去除能力的变化.结果表明,投加5%和15% 2,4-DCP复合高效菌的强化CAS系统,其对目标污染物的降解能力及抗负荷冲击能力得到显著提高.当系统受到间歇性2,4-DCP负荷冲击[110.37～171.60 mg/(L·d)]时,对于单次投菌后前30日内发生的间歇性负荷冲击,强化系统有效保持了对目标污染物的强化效果;在无2,4-DCP存在的情况下连续运行70d,当系统再次受到2,4-DCP负荷冲击时,强化系统的强化效果与前几次相比已明显下降,不能够快速有效去除污染物并维持系统稳定,因此有必要再次投加高效菌.     

Submerged vegetation removal promotes shift of dominant phytoplankton functional groups in a eutrophic lake

Historical data indicate that the dominance of submerged plants in Dianchi Lake in the 1960 s was characterized by low algal density with dominance of non-toxic group J（Scenedesmus,Pediastrum,etc.）. The removal of submerged plants,which began in the 1970 s,resulted in the expansion of bloom-forming Microcystis（group M）. Laboratory experiments suggested that Microcystis aeruginosa was inclined to grow and develop at elevated temperatures. The growth of Scenedesmus obliquus was slower than that of co-cultivated M. aeruginosa in the absence of Ceratophyllum demersum,especially at higher temperatures. The existence of submerged plant C. demersum could inhibit the growth of the harmful algae M. aeruginosa and this inhibitory effect by C. demersum was enhanced with an increase in temperature. Instead,with C. demersum,the growth of S. obliquus was not inhibited,but the co-cultivated M. aeruginosa was eliminated in a short time. Combined with the historical data and laboratory experiments,it was indicated that the submerged plants might play important roles in the dominance of the non-toxic group J in the historical succession. Consequently,the introduction of the submerged plant such as C. demersum might alter the dominant phytoplankton functional groups from M to J and benefit the restoration of the eutrophic lake.     

污水处理厂中红霉素抗药性基因的污染特征及选择性因子

采用固相萃取-高效液相色谱串联质谱(SPE-HPLC-MS/MS)检测分析了上海某污水处理厂中12种不同药品和个人护理品(pharmaceutical and personal care products,PPCPs)的含量水平和分布特征,采用实时荧光定量PCR方法定量检测分析了7种红霉素抗药性基因(ERY-ARGs)在污水处理厂中的分布和丰度变化.结果表明,在污水处理厂中共检出5种PPCPs(包括磺胺甲唑、红霉素、四环素、卡马西平和三氯生),浓度范围分别为24.5~38.7、47.5~49.2、43.1~85.4、2.5~3.9和423.2~8 973.3ng·L-1.两段A/O生物处理工艺对三氯生具有较好的去除效果,但对其余4种PPCPs的去除效果较差.与此同时,目标ERY-ARGs在污水处理厂中均被检出,在原水中的丰度达9.28×103(erm A)~1.83×108(ere A)copies·L-1,虽然两段A/O工艺能够显著降低污水中的ERY-ARGs(1.19 log~3.97 log),但其在最终处理出水中的浓度仍然较高.通过相关性分析可知,ERY-ARGs与红霉素和三氯生之间均具有显著相关性(P<0.05),表明污水处理厂中红霉素对ERY-ARGs的产生和传播具有重要影响,而三氯生对ERY-ARGs可能存在交叉选择性作用.     

上海市大气细菌污染研究

采用平皿沉降法对上海市６个采用点的大气细菌，进行了为期一年的监测，并进行了菌株鉴定和影响因素的研究分析，结果表明，上海市全年大气细菌数量变化曲线呈双峰型；空气中优势菌群为：微球菌属，葡萄球菌属，奈瑟氏菌属，干燥棒状杆菌属和芽孢杆菌属等。     

球衣细菌胞内PHB的提取和精制

报道了一种从球衣细菌胞内提取和精制PHB的有效方法。通过红外光谱、紫外光谱及1H谱分析得知 ,利用该方法制得的PHB精制品在结构上与标准品 (美国Sigma公司提供 )一致 ,纯度达 99 4 %以上。     

氚水在大豆土壤系统中的迁移与分布

采用模拟污染物的同位素示踪技术研究氚水在大豆-土壤模拟生态系统中的迁移、分布规律.通过为期50d的模拟试验,测定了植物和土壤样品中2种形态氚(自由水氚和结合态氚)的比活度.结果表明:引入土壤中的氚水,不仅在系统各分室间转移和分配,而且迅速向系统外散逸;氚水中的氚以自由水氚和结合态氚形态存在于大豆植株和土壤中;大豆植株中的自由水氚比活度于6h时即达最大值(根19.4Bq·g^-1;茎叶12.3Bq·g^-1),随后便逐渐下降,而结合态氚呈缓慢增加;大豆根中的总氚比活度开始时高于茎叶中的比活度,而后趋于平衡,表层土中2种形态氚基本呈逐渐下降.运用示踪动力学分室模型原理对实验数据拟合得:土壤中的比活度C_s=88.37e^-11.847t+7.38e^-0030t;大豆植株中的比活度C_b=10.30(e^-0.030t-e^-11.847t).     

介质阻挡放电等离子体直接分解NOx的影响因素

在以 γ- Al₂O₃小球作为填充物的介质阻挡放电条件下 ,研究放电电压 ( 9～ 16k V)、交流电源频率 ( 50～ 1600 Hz)、NO入口浓度 ( 50～1800 ml/m³)、气体空速 (1000～ 6500 h^-1)、反应温度 ( 20～250℃ )、介质小球比表面积及加入 O₂等因素对 NO分解率的影响 .发现提高放电电压、放电频率及介质小球比表面积能显著增加 NO分解率 ,O₂ 的加入对 NO的等离子体分解有强抑制作用 .     

pH过程控制对铁炭微电解-Fenton影响中试研究

采用铁炭微电解-Fenton联合工艺处理制药废水生化出水,探讨了初始pH对微电解过程COD降解速率、出水中Fe2+和Fe3+变化规律以及后续Fenton氧化效果的影响,为优化联合工艺提出了微电解反应pH过程控制的理论。采用pH过程控制时,微电解对COD降解速率大大提高,降解过程基本符合零级反应动力学,同时可大大提高Fe2+和Fe3+浓度及总铁析出量。试验结果表明:当初始pH=2.5,以3.0L/h连续性投加稀硫酸100 min,曝气微电解反应2 h,出水再投加1.0mL/L的H2O2进行Fenton氧化2 h,出水COD总去除率可达85.6%;采用pH过程控制可将微电解出水ρ(Fe2+)浓度从48.6 mg/L提高至149 mg/L,COD降解速率从10.9 mg/(L·h)提高至23.8 mg/(L·h)。     

Hydroxyl, hydroperoxyl free radicals determination methods in atmosphere and troposphere

The hydroxyl radical (?OH) has a crucial function in the oxidation and removal of many atmospheric compounds that are harmful to health. Nevertheless, high reactivity, low atmospheric abundance, determination of hydroxyl, and hydroperoxyl radical's quantity is very difficult. In the atmosphere and troposphere, hydroperoxyl radicals (HO₂) are closely demanded in the chemical oxidation of the troposphere. But advances in technology have allowed researchers to improve the determination methods on the research of free radicals through some spectroscopic techniques. So far, several methods such as laser-induced fluorescence (LIF), high-performance liquid chromatography (HPLC), and chemical ionization mass spectroscopy have been identified and mostly used in determining the quantity of hydroxyl and hydroperoxyl radicals. In this systematic review, we have advised the use of scavenger as an advance for further researchers to circumvent some of these problems caused by free radicals. The primary goal of this review is to deepen our understanding of the functions of the most critical free radical (?OH, HO₂) and also understand the currently used methods to quantify them in the atmosphere and troposphere.     

A metal-OH group modification strategy to prepare highly-hydrophobic MIL-53-Al for efficient acetone capture under humid conditions

A series of highly-hydrophobic MIL-53-Al (MIL = Materials of Institut Lavoisier) frameworks synthesized via decoration of the Al-OH groups by alkyl phosphonic acid were developed as adsorbents for removing acetone from humid gas streams. The newly prepared materials were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM), N₂ adsorption-desorption and thermogravimetric analysis (TGA). Their adsorption behaviors toward acetone vapor under dry and wet conditions were studied subsequently. Results showed that alkyl phosphonic acid was successfully grafted into MIL-53-Al skeleton through coordinating interaction with Al³⁺ generating [email protected]_x (x = 12, 14, 18). The [email protected]_x exhibited similar crystal structure and thermal stability to parent MIL-53-Al. Furthermore, the modified materials showed significantly enhanced hydrophobicity. The water vapor uptake of [email protected]₁₄ decreased by 72.55% at 75% relative humidity (RH). Dynamic adsorption experiments demonstrated that water vapor had almost no effect on the acetone adsorption performance of [email protected]₁₄. Under the condition of 90% RH, the acetone adsorption capacity of [email protected]₁₄ was 102.98% higher than that of MIL-53-Al. Notably, [email protected]₁₄ presented excellent adsorption reversibility and regeneration performance in 10 adsorption-desorption cycles. Taken together, the strategy of metal-OH group modification is an attractive way to improve the acetone adsorption performance over metal-organic frameworks (MOFs) under humid conditions. Besides, [email protected]₁₄ would be deemed as a promising candidate for capturing acetone in high moisture environment.