The role of condensed organic matter in the nonlinear sorption of hydrophobic organic contaminants by a peat and sediments

This study examines the effect of soil organic matter heterogeneity on equilibrium sorption and desorption of phenanthrene, naphthalene, 1,3,5-trichlorobenzene (1,3,5-TCB), and 1,2-dichlorobenzene (1,2-DCB) by soils and sediments. Two estuary sediments, a Pahokee peat (PP; Euic, hyperthermic Lithic Haplosaprist), and two subsamples (base- and acid-treated peat [TP] and acid-treated peat [FP]) of the peat were used as the sorbents. The contents of black carbon particles were quantified with a chemical extraction method. Petrographical examinations revealed the presence of the condensed soil and sediment organic matter (SOM) in Pahokee peat. The Freundlich isotherm model in two different forms was used to fit both sorption and desorption data. The results show that the sorption and desorption isotherms are generally nonlinear and that the apparent sorption-desorption hysteresis is present for phenanthrene and TCB. Detailed analysis of sorption data for the tested sorbent-sorbate systems indicates that black carbon is probably responsible for sorption isotherm nonlinearity for the two sediments, whereas the humic substances and kerogen may play the dominant role in nonlinear sorption by the peat. This investigation suggests that the microporosity of SOM is important for the hydrophobic organic contaminant (HOC) sorption capacity on the peat.     

Soil and litter phosphorus-31 nuclear magnetic resonance spectroscopy: extractants, metals, and phosphorus relaxation times

Phosphorus-31 nuclear magnetic resonance (NMR) spectroscopy is an excellent tool with which to study soil organic P, allowing quantitative, comparative analysis of P forms. However, for 31P NMR to be tative, all peaks must be completely visible, and in their correct relative proportions. There must be no line broadening, and adequate delay times must be used to avoid saturation of peaks. The objective of this study was to examine the effects of extractants on delay times and peak saturation. Two samples (a forest litter and a mineral soil sample) and three extractants (0.25 M NaOH, NaOH plus Chelex (Bio-Rad Laboratories, Hercules, CA), and NaOH plus EDTA) were used to determine the differences in the concentration of P and cations solubilized by each extractant, and to measure spin-lattice (T1) relaxation times of P peaks in each extract. For both soil and litter, NaOH-Chelex extracted the lowest concentrations of P. For the litter sample, T1 values were short for all extractants due to the high Fe concentration remaining after extraction. For the soil sample, there were noticeable differences among the extractants. The NaOH-Chelex sample had less Fe and Mn remaining in solution after extraction than the other extractants, and the longest delay times used in the study, 6.4 s, were not long enough for quantitative analysis. Delay times of 1.5 to 2 s for the NaOH and NaOH-EDTA were adequate. Line broadening was highest in the NaOH extracts, which had the highest concentration of Fe. On the basis of these results, recommendations for future analyses of soil and litter samples by solution 31P NMR spectroscopy include: careful selection of an extractant; measurement of paramagnetic ions extracted with P; use of appropriate delay times and the minimum number of scans; and measurement of T1 values whenever possible.     

废钻井液固化实验研究

利用经实验筛选的固化剂配方对废钻井液进行了固化处理的室内配方研究。结果表明,经该固化剂配方处理后的固结材料在水中浸泡5d后的浸出液在色度、化学需氧量、pH值、石油类、悬浮物含量和重金属含量等指标方面可达到国家《污水综合排放标准》(GB8978-1996)中的二级标准。     

催化湿式氧化法处理吡虫啉农药废水

自制了Cu／Mn，Cu／Ce，Cu／Ni，Ce／Mn，Ce／Ag等催化剂，经过性能比较，选择催化活性较高且金属溶出量较小的Cu／Ni作催化剂。用催化湿式氧化法处理吡虫啉农药废水，考察了各种因素对处理效果的影响。实验结果表明：在进水pH为6．93、Cu／Ni加入量为4．0g、反应温度为190oC、氧分压为1．6MPa、反应时间为120min的条件下，COD去除率为95％；处理后废水的BOD5／COD从0．093增至0．590，可生化性明显改善。     

岩溶地基土洞塌陷评价及处理

地下水(地表水)产生的渗透潜蚀作用、崩解作用等是土洞形成和发展的重要原因。对工程实例中的土洞,采用极限平衡法和压力拱分析法进行了稳定性判别。在土洞中充填砼,然后采用压力灌浆,灌浆所采用的水灰比为1∶1~1∶1.5,灌浆压力一般为0.15~0.30 MPa,地基处理效果好。     

节能减排 实现钢铁企业可持续发展

通过对钢铁行业消耗水资源及产生污染情况进行分析，阐述了目前钢铁行业为节能减排而采取的管理、技术、污染治理措施，以达到减少废水外排量、降低污染物浓度、降低新水消耗的目的，对钢铁行业废水回用中尚存和潜在的工艺、设计问题进行了讨论，同时提出了通过清洁生产、优化工艺结构来解决问题的措施和建议，确立了企业近期和长期的节能减排任务目标。     

在线衍生化吹扫捕集-气相色谱/质谱分析水中的五氯酚

建立了通过乙酸酐衍生化-吹扫捕集-气相色谱／质谱分析水中五氯酚的新方法，探讨了吹扫时间、样品池温度、离子强度以及衍生化试剂的加入量等条件对捕集效果的影响。结果表明：采用吹扫时间25min、样品池温度60℃、离子强度20％氯化钠以及衍生化试剂的量200μl等条件对水中的五氯酚有较好的捕集效果，用于水中五氯酚的测定，结果满意。     

Highly selective capture of phosphate ions from water by a water stable metal-organic framework modified with polyethyleneimine

Environmental Science and Pollution Research - In this work, a series of polyethyleneimine (PEI) impregnated metal-organic framework (UiO-66) with varying PEI loadings were prepared and applied as...     

Detailed Ecological Footprint Accounting of Liaoning in 2006

Ecological footprint （EF） has received considerable attention as a useful indicator in the context of sustainable development. So far, EF has been used in numerous studies by academies, organizations and government authorities. However, the results of these studies failed to be comparable directly with each other due to imprecise data sets, unmodified accounting methods of pasture and fossil energy, ignored secondary products, undefined process Of calculating yield factors and improper biocapacity for biodiversity. In this paper, we elaborated on EF estimating methods from six categories of consumption in order to overcome the limitations above. We adopted precise data and revised methods, calculated EF of some secondary products, introduced weighted factor to calculate yield factors and adjusted biocapacity by an appropriate amount. Meanwhile, we investigated the resource consumption of Liaoning Province in 2006 to assess EF. Its results showed that Liaoning Province overused its natural capital and was in an unsustainable state. We concluded that two specific problems that had arisen in EF assessment and gave some suggestions for Liaoning Province to improve its unsustainable state.