进水氨氮浓度对好氧/缺氧/延长闲置SBR脱氮除磷性能的影响

以合成废水为研究对象,考察了不同进水氨氮浓度(20,40和60 mg/L)条件下好氧/缺氧/延长闲置SBR的脱氮除磷效果,并通过分析典型周期内氮磷元素及微生物体内各储能物质的变化,探究了进水氨氮浓度对好氧/缺氧/延长闲置SBR脱氮除磷性能的影响机理.结果表明,进水氨氮浓度为20,40和60 mg/L时,系统总磷(TP)去除率分别为96.6%、90.1%和81.8%,总氮去除率分别为93.1%、74.9%和60.0%.研究表明,进水氨氮浓度可影响好氧释磷与吸磷、聚羟基脂肪酸酯(PHAs)合成、缺氧反硝化以及闲置段释磷.进水氨氮浓度越高,用于微生物生长的碳源越多,PHAs的合成量越少,则好氧段吸磷减少;较高的进水氨氮浓度使缺氧段反硝化不彻底,较多的硝态氮将抑制下一周期好氧段释磷,系统脱氮除磷性能减弱.     

催化湿式氧化法处理有机废水的催化剂研究

催化湿式氧化法是处理高浓度、有毒有害、难降解有机废水的一种有效手段.本文分析总结了过渡金属、贵金属和稀土金属等作为均相催化剂与非均相催化剂,采用催化湿式氧化法处理有机废水的性能,特别是比较了它们处理多种有机废水时对COD的去除效率和载体的使用情况.从分析中可以看出,氧化铝是非常好的载体,多组分复合催化剂比单组分催化剂具有更好的催化性能,以Cu、Mn、Ce为主要活性组分的复合催化剂具有很高的催化活性,并且应用范围广.最后探讨了催化剂的反应机理和发展前景.     

水和废水中多种金属元素ICP－AES通用测定方法的研究

研究水和废水中多种元素ＩＣＰ－ＡＥＳ的通用分析方法，探讨了样品的前处理过程、最佳实验条件的选择、干扰的判断和校正及在整个分析过程中应注意的问题等。实验结果表明：此方法准确可靠，测定值基本能很好地与质控样的标准值相符合，加人回收率多在９０％－１１０％范围内，精密度多低于５％，检出限为０．ｌ—１００μｇ／Ｌ，线性分析范围达４—６个数量级。该方法简便快速易于掌握，可同时进行多元素分析。     

Distribution of PAEs in the middle and lower reaches of the Yellow River, China

Samples of water, sediment and suspended particulates were collected from 13 sites in the middle and lower reaches of the Yellow River in China. Phthalic acid esters (PAEs) concentrations in different phases of each sample were determined by Gas Chromatogram GC-FID. The results are shown as follows: (1) In the Xiao Langdi–Dongming Bridge section, PAEs concentrations in water phase from the main river ranged from 3.99 × 10⁻³ to 45.45 × 10⁻³ mg/L, which were similar to those from other rivers in the world. The PAEs levels in the tributaries of the Yellow River were much higher than those of the main river. (2) In the studied branches, the concentration of PAEs in sediment for Luoyang Petrochemical Channel (331.70 mg/Kg) was the highest. The concentrations of PAEs in sediment phase of the main river were 30.52 to 85.16 mg/Kg, which were much higher than those from other rivers in the world. In the main river, the concentration level of PAEs on suspended solid phases reached 94.22 mg/Kg, and it reached 691.23 mg/Kg in the Yiluo River – one tributary of the Yellow River. (3) Whether in the sediment or on the suspended solid phases, there was no significant correlation between the contents of PAEs and TOC or particle size of the solid phase; and the calculated Koc of Di (2-Ethylhexyl) Phthalate (DEHP) in the river were much less than the theoretical value, which inferred that PAEs were not on the equilibrium between water and suspended solid phases/sediment. (4) Among the measured PAEs compounds, the proportions of DEHP and di-n-butyl phthalate (DBP) were much higher than the others. The concentrations of DEHP exceeded the Quality Standard in all the main river and tributary stations except those in the Mengjin and Jiaogong Bridge of the main river. This indicates that more attention should be paid to pollution control and further assessment in understanding risks associated with human health.     

污泥中活性铝的溶出及形态分布

利用KCl,NH4Ac,HCl,NaOH四种化学浸提液将污水厂初沉污泥中的活性铝溶出,根据不同的溶出机理,得到铝的委员长中化学形态,进行定量测定,得到污泥中活性铝的形态分布,为污泥的合理利用提供一些信息。     

Impact of irreversible sorption of phthalate acid esters on their sediment quality criteria

The equilibrium partitioning (EqP) method has been applied to establish sediment quality criteria (SQC); however, it does not consider the nonlinear irreversible sorption of many organic contaminants. In this research, the sorption and desorption of two phthalate esters (PAEs), dimethyl phthalate (DMP) and di(2-ethylhexyl) phthalate (DEHP), in four natural sediments collected from the Yangtze River and the Yellow River were studied; the impact of irreversible sorption of DMP and DEHP on SQC has been evaluated. Based on the reversible and irreversible biphasic sorption model, the values of maximum irreversible sorption capacity (q(max)(irr)) were 125.19 μg g(-1)-337.37 μg g(-1) for DMP and 515.87 μg g(-1)-591.40 μg g(-1) for DEHP. The q(max)(irr) value was positively related to the organic carbon and black carbon contents, cation exchange capacity, and surface area of the sediments. The values of the irreversible sorption coefficient K(oc)(irr) for both DEHP and DMP in the four sediments approximated to a constant of 10(6.46 ± 0.38), which was 1-2 orders of magnitude higher than their reversible sorption coefficient K(oc)(irr). The values of SQC for PAEs based on the EqP method were modified by involving the irreversible sorption. The modified SQC of DEHP could be 2 to 20 times higher than the value predicted by the EqP method, and the assessment results for DEHP contamination in the sediments with the modified SQC were more reasonable than those with the non-modified SQC. It indicated that the current SQC based on the EqP method may be unnecessarily strict for specific organic compounds and the irreversible sorption should be taken into account.     

Allelopathic interactions between Skeletonema costatum and Alexandrium minutum

Potential allelopathic interactions between Skeletonema costatum and Alexandrium minutum were investigated using mixed cultures and culture filtrate in nutrient-replete medium. A. minutum growth was inhibited when grown in S. costatum filtrate, with the inhibitory effect directly proportional to the percentage of filtrate added. This demonstrates that the release of allelopathic compounds caused the growth inhibition. In contrast, the filtrate of A. minutum exerted no allelopathic activity on S. costatum. An autoinhibitory compound (15(S)-HEPE) extracted and purified from S. costatum culture was added to cultures of both S. costatum and A. mintum. This substance could depress S. costatum growth, but showed no significant inhibitory activity on A. minutum. This documented a second type of allelochemical interaction, termed auto-allelopathy, caused by a different compound from the one or ones that affected A. minutum in the co-cultures with added crude filtrate. Further studies are needed to explore the relative importance of these two types of allelopathy as factors influencing the competition between S. costatum and A. minutum in the field. Furthermore, given the observed decrease in diatom dominance relative to dinoflagellates with increasing eutrophication, one can predict that toxic species like A. minutum might become more prevalent in the future in the East China Sea if the trend of increasing pollution of coastal waters continues.     

Laboratory assessment of uptake and toxicity of lanthanum (La) in the leaves of Hydrocharis dubia (Bl.) Backer

Increasing amounts of lanthanum (La) is released into aquatic environments. However, little information is available on the influence of La on aquatic plants. In this study, physiological and ultrastructural responses of Hydrocharis dubia (Bl.) Backer leaves to elevated concentrations of La (up to 160???M) were investigated. The accumulation of La was found to be increased in a concentration-dependent manner. La disturbed the intrinsic balance of nutrient elements (P, Mg, Ca, Fe, K, and Zn). Pigment content decreased with the rise of the La concentrations and the EC₅₀ value for chlorophyll was 20???M on day?7. The antioxidants (superoxide dismutase, peroxidase, catalase, reduced ascorbate, and reduced glutathione) exhibited varied response to the La treatments. Malondialdehyde content enhanced gradually at all La concentrations. The enhancement in proline content was found in a concentration-dependent manner. The amounts of three polypeptides with apparent molecular weights of 61.9, 51.5, and 16.7?kDa, respectively, were gradually diminished, as well as one existing polypeptides with apparent molecular weight of 22.3?kDa, elevating in response to increasing La concentrations. Significant damage to the chloroplast, mitochondrion, and nucleus was imposed by La indicated a general disarray in the cellular functions. The negative effects of La on H. dubia unequivocally indicate that La could exert an adverse influence on aquatic ecosystem and should lead to a more careful discharge of such elements into water environment.     

热处理对脱水污泥溶解特性及厌氧消化性能的影响

分别对脱水污泥在100、130和170℃条件下进行热处理,研究热处理对脱水污泥溶解特性的影响。此外,在半连续式完全混合反应器中进行厌氧消化实验研究不同热处理污泥的厌氧消化性能。实验结果表明,在100、130和170℃条件下,污泥COD溶解率由处理前的5.23%分别提高至20.08%、22.50%和27.20%,脱水污泥热处理规律和效果与高含水率污泥(总固体含量<5%)基本一致。经130℃2 h和170℃30 min高温热处理后污泥甲烷产率显著提高,较原泥分别提高24.64%和38.61%,沼气中甲烷含量稍有降低。