金属浓度,半透膜孔径,水温及配位体对半透膜囊吸收铜的影响

在实验室条件下，研究了影响树脂－半透膜囊吸收铜的主要因素，重点探讨了水相铜含量，半透膜孔径，温度以及天然河水中的有机配位体对吸收的影响。结果表明，半透膜囊吸收量与水相游离铜浓度，水温及半透膜孔径的非整数次幂成正比，其中包括ＥＤＴＡ，河水富里酸，以及河水中的各种天然有机物在内的配位体均与铜生成不能被半透膜囊吸收的络合物，研究结果进一步证实了半透膜囊对水环境中游离态微量金属进行长期监测的可行性。     

南黄海鳀鱼产卵场大型底栖生物次级生产力研究

根据2001至2003年南黄海鳀鱼产卵期在鳀鱼产卵场33个站考察采集的大型底栖生物定量样品资料,利用Brey's(1990)的经验公式对调查海区进行了大型底栖生物栖息密度、生物量、次级生产力和P/B值的研究计算.结果表明,该海域大型底栖生物平均栖息密度为194.3 ind.m-2,平均生物量以去灰干重计,为4.08 g m-2,平均次级生产力以去灰干重计,为4.09 g m-2a-1.研究表明,生物量和次级生产力受水深的影响.平均P/B值在研究海域为1.32a-1.对研究结果与整个南黄海、渤海和东海的结果进行了比较与讨论,证明生产力随水深的加大而降低,P/B值随水温升高而升高.图2表1参25     

杭州城市及其边缘区湿地磷化学特征的研究

对杭州城市及其边缘区湿地土壤的磷形态组成、固磷能力和释放潜力等方面进行了初步的研究。结果表明,杭州城市及边缘地区的湿地由于受人类影响的不同及所处环境的差异,性质已有很大的分异。城区的西湖、水塘和河流底泥中磷的积累、磷的饱和度和零吸附磷平衡浓度均明显高于城市边缘地区的湿地;湿地土壤中的磷主要呈不稳定、或亚稳定态,可提取态磷约占总磷的80%,62%的湿地土壤磷饱和度在25%以上。最大磷吸附量的大小主要与湿地中无定形氧化铁、铝含量有关。零吸附时磷的浓度(EPC)较高,在0.10~2.48mg·L-1之间,具有较强的释放潜力。半透膜渗析法测得的磷释放量与磷积累呈正相关,但当磷饱和度超过25%时,其磷释放量显著增加。研究表明杭州市及其边缘区湿地土壤磷已普遍达到较高水平,这在一定程度上影响磷净化功能的正常发挥。     

臭氧与TiO2/UV协同降解对氯苯酚

利用O3／UV、TiO2／UV和O3／TiO2／UV降解对氯苯酚表明，臭氧与TiO2／UV具有明显的协同作用，如在本实验条件下降解5min后，上述3者对对氯苯酚的去除率分别为55％、10％和77%。O3／TiO2／UV协同作用的本质是由于臭氧能带走二氧化钛光致电子空穴对中的电子，从而产生了更多的羟基自由基，加速了有机物的降解。     

Induced alkoxyresorufin-O-dealkylases in tilapias (Oreochromis niloticus) from Guandu river, Rio de Janeiro, Brazil

The activity of fish monooxygenases has been extensively used as a monitoring tool to detect contamination of water bodies by cytochrome P450-inducing agents. In this study we evaluated the activities of ethoxy- (EROD), methoxy- (MROD) and pentoxy- (PROD) resorufin-O-dealkylases in the liver of Nile tilapias (Oreochromis niloticus) collected at the Guandu river, at a reference clean site (Lake 1) and at two other sampling sites (Lakes 2 and 3) in Rio de Janeiro state, Brazil. Alkoxyresorufin-O-dealkylases were measured fluorimetrically in the hepatic S9 fraction. EROD (17.7-fold), MROD (14.2-fold) as well as PROD activities were considerably higher in tilapias from Guandu river. A moderate increase of EROD (5.0-fold) and MROD (5.4-fold) was also found in tilapias from Lake 3. These findings suggest that Guandu river watershed, the main source of urban drinking water supply in Rio de Janeiro, is polluted with CYP1A-inducing xenobiotics. Furthermore, we also found a good linear relationship between EROD and MROD, a finding that agrees with the hypothesis that the two reactions are catalysed by the same CYP1A isoform in O. niloticus.     

Synchronous-scan fluorescence spectra of Chlorella vulgaris solution

The characterization of the Chlorella vulgaris solution was carried out using synchronous-scan spectroscopy. The range of concentration of algae and Fe(III) in aqueous solutions were 5 × 10⁸–8 × 10⁹ cells l⁻¹ and 10–60 μM, respectively. Effective characterization method used was synchronous-scan fluorescence spectroscopy. The wavelength difference (Δλ) of 90 nm was maintained between excitation and emission wavelengths; 90 nm was found to be the best Δλ for effective characterization of Chlorella vulgaris solution with or without quencher species (e.g., Fe(III), humic acid (HA)) for the first time. The peak was observed at about EX 236.6 nm/EM 326.6 nm for synchronous-scan fluorescence spectra. The fluorescence quenching of algae in system of algae–Fe(III)–HA was studied using synchronous-scan spectroscopy for the first time. Fe(III) was clearly the effective quencher. The relationship between I₀/I (quenching efficiency) and c (concentration of Fe(III) added) was a linear correlation for the algae solution with Fe(III). Also, Aldrich humic acid was found to be an effective quencher. pH effect on synchronous-scan fluorescence intensity of algal solution with Fe(III) and/or HA was evident.     

Solubilization of substituted indole compounds by beta-cyclodextrin in water

The solubilization of four pairs of substituted indole compounds (SICs) by β-cyclodextrin (β-CD) in water was investigated. The results show that 1,2,3,4-tetrahydrocarbazole and N-methyl-1,2,3,4-tetrahydrocarbazole form 1:1 inclusion complexes with β-CD, while the other six SICs form 1:2 inclusion complexes, respectively. To each pair of SICs with similar structures, the differences between their solubilization in β-CD/water solutions has been explained by the difference of their contact area within the β-CD cavity, the difference of their molecule polarity, or the presence of hydrogen bond between SIC molecule and β-CD molecule.     

制备条件对Fe/AC脱硫活性的影响

考察了Fe/AC脱硫剂的煅烧温度和载铁量对脱硫活性的影响，并对脱硫剂进行了X－射线衍射（XRD）和EXAFS表征，结果表明：经250℃煅烧的Fe/AC脱硫剂具有最高的脱硫活性，200℃煅烧，前驱体未完全分解，高于250℃煅烧，会使活性组分聚集，二者均导致脱硫活性降低。Fe/AC脱硫剂适宜的载铁量为3．5－14％，大于14％担载量使脱硫剂微孔堵塞严重，致使其脱硫活性下降。     

Degradation of Benzo[a]Pyrene in Soil with Arbuscular Mycorrhizal Alfalfa

Mycorrhizal and non-mycorrhizal alfalfa (Medicago sativa) was grown in pots containing soil artificially contaminated with various levels of benzo[a]pyrene (B[a]P)(0, 1, 10 and 100 mg kg^–1). Soil and plants were sampled after 30, 40, 50, 60 and 90 days and compared with unlanted pots. The percentage of mycorrhizal root length colonized by Glomus caledoniun was not significantly affected by the addition of B[a]P up to 10 mg kg^–1 but was significantly lower at 100 mg kg^–1B[a]P compared with low concentrations (p < 0.05). There was no difference in soil polyphenol oxidase and dehydrogenase activity among the controls and applications of 1 and 10 mg kg^–1 of B[a]P. However, enzyme activities were significantly higher at 100 mg kg^–1B[a]P compared with the other three treatments, and there was no mycorrhizal effect. Over a period of 90 days the concentration of B[a]P in soil in which alfalfa was grown was significantly lower than in unplanted soil (p < 0.05). Degradation rates of B[a]P added at 1, 10 and 100 mg kg^–1 without G. caledonium were 76, 78 and 53%, and with mycorrhizal inoculation were 86, 87 and 57%. The degradation rate in unplanted soil was significantly lower than in planted soil, and was significantly higher in medium- and low-B[a]P treatments than in the high B[a]P concentration tested. There is a possibility of enhancement phytoremediation of PAHs in rhizosphere soil with arbuscular mycorrhizal fungi.     

17O-NMR研究Al(Ⅲ),Fe(Ⅲ)盐对水缔合的影响

测试了AlCl3,Al2(SO4)3,FeCl3,Fe2(SO4)3等对水的^17O-NMR化学位移和半峰宽的影响。并利用水^17O-NMR化学位移和半峰宽的变化与氢键的关系，分析了AlCl3,Al2(SO4)3。FeCl3,Fe2(SO4)3等对水缔合的影响，研究表明，AlCl3,Al2(SO4)3。FeCl3,Fe2(SO4)3等对水缔合有促进作用。且Fe^3 对水缔合的作用大于Al^3 。