垃圾焚烧飞灰磷酸洗涤对重金属的固定效应研究

重金属的固定是垃圾焚烧飞灰资源化技术的核心问题.通过系统试验,研究了垃圾焚烧飞灰磷酸洗涤对重金属溶出、后续烧结过程中重金属挥发,以及重金属化学形态变迁的影响.试验结果表明,磷酸洗涤在有效洗脱飞灰中氯盐的情况下,能够显著减少洗涤过程中重金属的溶出,抑制烧结过程中重金属的挥发,从而避免了飞灰处理过程的二次污染;同时,磷酸洗涤使飞灰中的重金属在烧结前后均向更为稳定的化学形态转化,烧结产物中重金属主要以残留态存在,从而提高了烧结产物资源化利用的长期环境安全性.     

城市生活污泥烧结制陶粒的两种工艺比较研究

通过试验比较了"湿法造粒-烧结"和"干化-烧结"2种利用城市生活污泥烧结制陶粒的工艺路线.分析了工艺路线、原料配比和烧结温度对污泥陶粒的产品强度、吸水率和密度等性能指标的影响,同时指出了沸石粉和粘土作为助熔剂的不同作用机理和作用温度.实验结果表明,污泥"干化-烧结"制陶粒更有优势.烧结陶粒不会造成二次污染.综合考虑产品性能与经济性,适宜的物料配比为干污泥50%、粉煤灰30%～40%、粘土10%～20%.     

把安全理念贯穿于企业管理的全过程

众所周知,坚持以人为本、安全发展、切实维护好职工群众的身体健康和生命安全,这既是新形势下认真贯彻落实科学发展观的重要内容,也是切实构建和谐社会和打造安全本质型企业的应有之义。近年来,职工队伍分布重庆、山西、贵州和四川等省市几十个工点流动施工的重庆能投巨能集团一公司坚持“把安全生产贯穿企业管理全过程”,并辅之系列以人为本保安全生产的工作措施,     

MnOx/介孔γ-Al2O3催化臭氧化降解水中安替比林的研究

以自制的介孔γ-Al₂O₃为载体,通过等体积浸渍法合成了MnO_x/介孔γ-Al₂O₃催化剂。采用X射线衍射(XRD)、透射电镜 (TEM) 以及紫外可见漫反射（UV-Vis DRS）等手段对其进行表征。结果表明,锰氧化物在介孔氧化铝载体上具有较高的分散度,并且锰以多种价态存在。高度分散以及多价态的MnO_x能够提高催化臭氧化过程中电荷转移,引起更高     

Equilibrium and kinetics of adsorption of phosphate onto iron-doped activated carbon

Purpose

Two series of activated carbons modified by Fe (II) and Fe (III) (denoted as AC/N-Fe^II and AC/N-Fe^III), respectively, were used as adsorbents for the removal of phosphate in aqueous solutions.

Method

The synthesized adsorbent materials were investigated by different experimental analysis means. The adsorption of phosphate on activated carbons has been studied in kinetic and equilibrium conditions taking into account the adsorbate concentration, temperature, and solution pH as major influential factors.

Results

Maximum removals of phosphate are obtained in the pH range of 3.78?C6.84 for both adsorbents. Langmuir isotherm adsorption equation well describes the experimental adsorption isotherms. Kinetic studies revealed that the adsorption process followed a pseudo-second order kinetic model. Results suggest that the main phase formed in AC/N-Fe^II and AC/N-Fe^III is goethite and akaganeite, respectively; the presence of iron oxides significantly affected the surface area and the pore structure of the activated carbon.

Conclusions

Studies revealed that iron-doped activated carbons were effective in removing phosphate. AC/N-Fe^II has a higher phosphate removal capacity than AC/N-Fe^III, which could be attributed to its better intra-particle diffusion and higher binding energy. The activation energy for adsorption was calculated to be 22.23 and 10.89 kJ mol^?1 for AC/N-Fe^II and AC/N-Fe^III, respectively. The adsorption process was complex; both surface adsorption and intra-particle diffusion were simultaneously occurring during the process and contribute to the adsorption mechanism.     

Assessment of typical pollutants in waterborne by combining active biomonitoring and integrated biomarkers response

Organic pollutants, heavy metals and pharmaceuticals are continuously dispersed into the environment and have become a relevant environmental emerging concern. In this study, a situ assay to assess ecotoxicity of mixed pollutants was carried out in three typical sites with different priority contaminations in Guangzhou, China. Chemical analysis of organic pollutants, metals and quinolones in three exposure sites were determined by GC-ECD/MS, ICP-AES and HPLC, as well as, a combination of biomarkers including: ethoxyresorufin O-deethylase (EROD); aminopyrine N-demethylase (APND); erythromycin N-demethylase (ERND); glutathione S-transferase (GST); malondialdehyde (MDA); CYP1A; and P-glycoprotein (P-gp) mRNA expressions were evaluated in Mugilogobius abei. Results of chemical analysis in sediment samples revealed that the dominant chemicals were organic pollutants and heavy metals in Huadi River while quinolones in the pond. Bioassays indicated that differences among sites were in relation to some specific biomarkers. EROD and GST activities significantly increased after 72 h in situ exposure, but no difference was observed among the exposure sites. APND, ERND and MDA exhibited dissimilar change patterns for different priority pollutants. CYP1A and P-gp mRNA expressions were significantly induced at all exposure sites, whilst P-gp activity was typical for S2 with the highest levels of quinolones. The molecular biomarkers seemed to be more susceptible than enzyme activities. These assays confirmed the usefulness of applying a large array of various combined biomarkers at different levels, in assessing the toxic effects of mixed pollutants in a natural aquatic environment.     

Plants' use of different nitrogen forms in response to crude oil contamination

In this study, we investigated Phragmites australis’ use of different forms of nitrogen (N) and associated soil N transformations in response to petroleum contamination. ¹⁵N tracer studies indicated that the total amount of inorganic and organic N assimilated by P. australis was low in petroleum-contaminated soil, while the rates of inorganic and organic N uptake on a per-unit-biomass basis were higher in petroleum-contaminated soil than those in un-contaminated soil. The percentage of organic N in total plant-assimilated N increased with petroleum concentration. In addition, high gross N immobilization and nitrification rates relative to gross N mineralization rate might reduce inorganic-N availability to the plants. Therefore, the enhanced rate of N uptake and increased importance of organic N in plant N assimilation might be of great significance to plants growing in petroleum-contaminated soils. Our results suggest that plants might regulate N capture under petroleum contamination.     

Distribution characteristics and source analysis of dioxins in sediments and mussels from Qingdao coastal sea

Seven of surface sediments, one sediment core and two mussel samples were collected from the Qingdao coastal sea of the western Yellow Sea and analyzed to determine the horizontal distribution, deposition flux, and toxicity equivalency (TEQs) of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs). The total PCDD/Fs concentrations in the surface sediments ranged between 10.7 and 428 ng kg(-1) dry wt. The horizontal distribution of PCDD/F congeners in the sediments was characterized by elevated concentrations at the locations in the east of Jiaozhou Bay with the highest concentration occurring near the Haibo River mouth. Physical parameters (total organic carbon contents and sediment types) and the current circulation systems in Jiaozhou Bay can be important factors controlling the horizontal distribution pattern of PCDD/Fs in the bay. The influence of the Haibo River as a source of pollution was evidenced by PCDD/F homologue profiles, indicating a contribution from sewage sludge in addition to other possible sources. Records from the sediment core revealed that the total PCDD/Fs in the Qingdao coastal sea were nearly constant since 1951 till 1980s and increased remarkably after 1980s. The total 2,3,7,8-substituted PCDD/Fs and total TEQs of PCDD/Fs on the lipid basis in the mussel sample inside the bay were significantly higher than in the adjacent sediment. The homologue profiles of PCDD/Fs in the mussels were quite different from those of the sediments, characterized by high TCDF (50% of the total PCDD/Fs).     

有机氯农药硫丹的生殖毒性及其机制研究进展

硫丹作为一种广谱有机氯农药,在农业区域周边的土壤和水体中都存在较高残留,2011年被斯德哥尔摩公约列入持久性有机污染物(POPs)名单。硫丹已被证实对神经系统、心血管系统、肝、肾等具有毒性作用,关于其生殖毒性的研究很多,但潜在机制尚不完全清楚。本文总结了硫丹导致的不同动物的生殖毒性,并从生殖器官和生殖细胞损伤、氧化应激以及DNA损伤、生殖细胞周期阻滞及细胞凋亡等方面,对近年来硫丹生殖毒性及其作用机制研究进展进行综述,并对其中存在的问题进行讨论,以期有助于深入了解硫丹的毒性效应。     

Characteristics and impacts of trace elements in atmospheric deposition at a high-elevation site,southern China

To investigate the regional background trace element (TE) level in atmospheric deposition (dry and wet), TEs (Fe, Al, V, Cr, Mn, Ni, Cu, Zn, As, Se, Mo, Cd, Ba, and Pb) in 52 rainwater samples and 73 total suspended particles (TSP) samples collected in Mt. Lushan, Southern China, were analyzed using inductively coupled plasma-mass spectrometry (ICP-MS). The results showed that TEs in wet and dry deposition of the target area were significantly elevated compared within and outside China and the volume weight mean pH of rainwater was 4.43. The relative contributions of wet and dry depositions of TEs vary significantly among elements. The wet deposition fluxes of V, As, Cr, Se, Zn, and Cd exceeded considerably their dry deposition fluxes while dry deposition dominated the removal of pollution elements such as Mo, Cu, Ni, Mn, and Al. The summed dry deposition flux was four times higher than the summed wet deposition flux. Prediction results based on a simple accumulation model found that the content of seven toxic elements (Cr, Ni, Cu, Zn, As, Cd, and Pb) in soils could increase rapidly due to the impact of annual atmospheric deposition, and the increasing amounts of them reached 0.063, 0.012, 0.026, 0.459, 0.076, 0.004, and 0.145 mg kg^?1, respectively. In addition, the annual increasing rates ranged from 0.05% (Cr and Ni) to 2.08% (Cd). It was also predicted that atmospheric deposition induced the accumulation of Cr and Cd in surface soils. Cd was the critical element with the greatest potential ecological risk among all the elements in atmospheric deposition.