长江徐六泾黑碳的季节变化及环境意义

2009年8月~2010年7月,每月在长江口徐六泾对水中悬浮颗粒物进行了采样,分析悬浮颗粒物中有机碳及黑碳含量,研究它们的季节变化特征,并计算出相应的输送通量。结果显示,水体中颗粒有机碳（Particulate organic carbon,POC）含量在034~092 mg/L,黑碳（Black carbon,BC）含量在0035~0096 mg/L;POC含量与水中总悬浮颗粒物（Total suspended material,TSM）含量有显著的正相关,但POC％随着TSM浓度的增加而减小;此外,水体中BC含量与人类的燃烧活动密切相关。观测期间长江的POC通量为234×106 t/yr,BC通量为277×105 t/yr,且BC通量占到颗粒有机碳通量的129%     

含硝基苯类化合物废水处理技术研究进展

综述了近年来处理含硝基苯类化合物废水的物理法（包括吸附法和溶剂萃取法）、化学法（包括电化学法、铁碳微电解法、超声波氧化法和臭氧氧化法及复合技术）和生物法的研究进展。指出将现有的处理技术高效整合并降低成本是今后处理含硝基苯类化合物废水的研究方向和重点。     

人工湿地基质对NH4＋-N吸附性能

为研究建筑废物红砖和工业废物煤渣用作人工湿地脱氮基质的可行性,分别通过静态吸附实验和动态NHf—N去除效果实验进行考察。结果表明,红砖和煤渣对NH4＋-N最大静态吸附量分别为0．2533mg／g和0．0533mg／g,其吸附等温曲线均符合Freundlich型吸附方程,吸附常数分别为0．0419和0．0091;红砖煤渣组合对污水中NH4＋-N平均动态脱除率达到41．18％,高于红砖的37．63％和煤渣的30．92％。     

以聚己内酯作为生物反硝化固体碳源的研究

为解决水体因低碳氮比而导致脱氮效率差的问题,将颗粒聚己内酯(PCL)重新塑形为阶梯环状,研究其作为反硝化过程的生物膜载体与固相碳源的反硝化性能。结果表明,在静态实验中,平均反硝化速率为8.57 mg NO3-N/(L·h);反硝化过程为零级反应。连续填充床实验中,超过90%的硝酸盐可被去除,出水NO2-N质量浓度低于0.20 mg/L;出水NH3-N质量浓度略有上升;出水溶解性有机碳(DOC)先上升后降低至1 mg/L左右。电子扫描显微镜扫描显示,PCL阶梯环反应表面空隙率较高,表面生物膜以杆菌为主,反应后被明显腐蚀;液相色谱检测显示PCL阶梯环分子量反应前后略有下降,其结构未受到破坏;表明该材料适合作为反硝化反应的碳源的同时,又可以作为载体供微生物附着生长。     

Comparison of lignin peroxidase and horseradish peroxidase for catalyzing the removal of nonylphenol from water

Concentrations of aqueous-phase nonylphenol (NP), a well-known endocrine-disrupting chemical, are shown to be reduced effectively via reaction with lignin peroxidase (LiP) or horseradish peroxidase (HRP) and hydrogen peroxide. We systematically assessed their reaction efficiencies at varying conditions, and the results have confirmed that the catalytic performance of LiP toward NP was more efficient than that of HRP under experimental conditions. Mass spectrum analysis demonstrated that polymerization through radical–radical coupling mechanism was the pathway leading to NP transformation. Our molecular modeling with the assistance of ab initio suggested the coupling of NP likely proceeded via covalent bonding between two NP radicals at their unsubstituted carbons in phenolic rings. Data from acute immobilization tests with Daphnia confirm that NP toxicity is effectively eliminated by LiP/HRP-catalyzed NP removal. The findings in this study provide useful information for understanding LiP/HRP-mediated NP reactions, and comparison of enzymatic performance can present their advantages for up-scale applications in water/wastewater treatment.     

Tree bark as a passive air sampler to indicate atmospheric polybrominated diphenyl ethers (PBDEs) in southeastern China

The different barks were sampled to discuss the influence of the tree species, trunk circumference, and bark thickness on the accumulation processes of polybrominated diphenyl ethers (PBDEs) from air into the bark. The results of different PBDE concentrations indicated that barks with a thickness of 0–3 mm collected from weeping willow, Camphor tree, and Masson pine, the trunk circumferences of which were 100 to 150 cm, were better PBDEs passive samplers. Furthermore, tree bark and the corresponding air samples were collected at Anji (AJ), Hangzhou (HZ), Shanghai (SH), and Wenling (WL) to investigate the relationship between the PBDE concentrations in bark and those in air. In addition, the significant correlation (r ²?=?0.906; P?<?0.05) indicated that atmospheric PBDEs were the principle source for the accumulation of PBDEs in the barks. In this study, the log K _BA (bark–air partition coefficient) of individual PBDE congeners at the four sites were in the range from 5.69 to 6.79. Finally, the total PBDE concentration in WL was 5 to 20 times higher than in the other three cities. The result indicated that crude household workshops contributed a heavy amount of PBDEs pollution to the environment, which had been verified by the spatial distribution of PBDEs levels in barks collected at Wenling (range, 26.53–1317.68 ng/g dw). The good correlation between the PBDE concentrations in the barks and the air samples and the variations of the PBDE concentrations in tree barks collected from different sites reflected that the bark could be used as a passive sampler to indicate the atmospheric PBDEs.     

Iron improving bio-char derived from microalgae on removal of tetracycline from aqueous system

Novel magnetic carbonaceous bio-char was hydrothermal prepared from microalgae under different loadings of iron and its structures and surface chemistry were characterized with Fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and nitrogen adsorption-desorption isotherm (BET). The morphology of bio-char changed from sheet to particle as iron loading increased and its surface area also increased. When 3.0 g of dried microalgae and 6.0 mmol iron salt ((NH₄)₂SO₄·FeSO₄·6H₂O) were mixed and treated, the obtained bio-char possessing the highest amount of oxygen-containing functional groups resulted in the best adsorption performance on tetracycline (TC). This adsorption process was fitted to Langmuir adsorption isotherm and the maximum adsorption capacity was 95.86 mg/g, which is higher than other bio-char reported. The iron loading contributed to the higher adsorption capacity of bio-char, which may be due to three factors, the high surface area, more hydrogen bonding, and bridging effects of the structural Fe for TC. Our data suggest that bio-char may have more important role in stabilization of pollutants in the environment.     

Medium optimization for the production of anti-cyanobacterial substances by Streptomyces sp. HJC-D1 using response surface methodology

Bioremediation using isolated anti-cyanobacterial microorganism has been widely applied in harmful algal blooms (HABs) control. In order to improve the secretion of activated anti-cyanobacterial substances, and lower the cost, a sequential optimization of the culture medium based on statistical design was employed for enhancing the anti-cyanobacterial substances production and chlorophyll a (Chl a) removal by Streptomyces sp. HJC-D1 in the paper. Sucrose and KNO₃ were selected as the most suitable carbon and nitrogen sources based on the one-at-a-time strategy method, and sucrose, KNO₃ and initial pH were found as major factors that affected the anti-cyanobacterial ability of the isolated stain via the Plackett–Burman design. Based on the response surface and canonical analysis, the optimum condition of culture medium was obtained at 22.73 g l^-1 of sucrose, 0.96 g l^-1 of KNO₃, and initial pH 8.82, and the Chl a removal efficiency by strain HJC-D1 increased from 63?±?2 % to 78?±?2 % on the optimum conditions.     

Simultaneous separation of apigenin,luteolin and rosmarinic acid from the aerial parts of the copper-tolerant plant Elsholtzia splendens

Elsholtzia splendens is a copper-tolerant plant species which grows on copper deposits in China. The generation of a valuable E. splendens biomass on specific contaminated sites has become one of the promising phytotechnologies. The simultaneous separations of apigenin, luteolin, and rosmarinic acid yielded in the ethyl acetate extracts of the flowering aerial parts was achieved by the use of a macroporous resin, polyamide, and silicagel columns during chromatography. Chemical identification confirmed the structures based on the spectra of FTIR, NMR, and HPLC/ESI-MS. The isolated compounds of purity above 98.3 % were evaluated for their in vitro cytotoxic activities against human cancer cell lines including A549 (non-small lung), A431 (skin), and Bcap37 (breast). Among these compounds, luteolin and apigenin presented the best cytotoxic activities against A549, A431, and Bcap37 cells and, therefore, both could be the valuable products for the post-harvest processing of E. splendens biomass.     

添加天然沸石和石灰对土壤镉形态转化的影响

采用土壤培养实验,研究镉污染土壤中添加沸石、石灰及两者配施对土壤pH值和土壤镉形态变化的影响。结果表明,土壤pH值随沸石用量的增加而增加,随培养时间呈现先增加后下降并逐渐趋于稳定的趋势,但均高于对照。高剂量石灰的处理对土壤pH的影响最大,与对照相比土壤pH提高了3.33个单位。在土壤5~50 d培养过程中,石灰处理的土壤交换态镉含量呈现先逐渐降低而后略有升高的趋势,其余处理均呈下降趋势。培养50 d后,高剂量的沸石、石灰及高剂量沸石与石灰配施处理的土壤交换态镉含量从5 d时的67.54、61.95和55.56 mg/kg降低至54.65、49.93和45.96mg/kg。相关分析表明,不同培养时期交换态镉含量与土壤pH值呈负相关关系。在10个处理中,L2Z3(石灰2 g/kg土和沸石60 g/kg土)组合处理效果最好,使土壤交换态镉含量下降了34.68%,碳酸盐结合态镉含量上升了4.30%,铁锰氧化结合态镉含量上升了16.97%,有机结合态镉含量上升了1.31%,残渣态镉含量上升了12.11%。