苏南典型河段磷的分布及释放特性研究

通过测定常州典型河段河水和底泥中的磷含量,同时分析了磷在不同底泥颗粒中含量分布的变化,阐述了河流中磷的分布和转移趋势。结果表明:河水中的磷含量通常低于底泥间隙水中的磷含量,但当河流发生富营养化后,底泥中的磷大量向上层水体释放,使得河水中的磷含量不断增加。底泥有效磷与总磷含量之间没有明显相关性,而与底泥间隙水的磷含量之间存在着交换平衡。底泥颗粒以2μm~50μm的粒级为主,即以细砂和粉砂质有机-无机聚合体矿物颗粒为主。磷在底泥颗粒中的含量随着底泥粒径的增大而减少,且粒径越大的颗粒对磷的吸附能力越弱,其中的磷向外释放的可能性越大。     

Research based on double coverage rate and reliability of gas detector layout optimization

The gas detector layout should be highly attuned to combustible gas leakage and attain a good reliability in avoiding detector malfunction, which is an important guarantee for the normal production of the chemical industry and other related enterprises. Herein, a gas detector layout optimization method based on double coverage and reliability is proposed. The key gas leakage monitoring area is determined through layout scene field investigation. To improve the detection probability and detection system reliability, the dual coverage target and voting mechanism are set, and the gas detector layout is determined with the ray-casting algorithm according to the coverage target. Combined with FLACS software to simulate a variety of typical leakage conditions under different layout scenarios, the relationship between the leaked gas concentration detected by gas detectors in each layout scheme and time is obtained, and the gas leakage detection probability in each layout scheme, number of detectors that can trigger the alarm, shortest time to trigger the alarm and reliability are comprehensively evaluated. The decision-maker selects the final gas detector layout plan according to the evaluation results and actual site needs. The study shows that the detection probability of each layout scheme set according to the double coverage is high, and multiple detectors can trigger the alarm (up to 100%), which ensures that the alarm can be triggered within 10 s under all applicable conditions. According to the evaluation results, the decision-maker can obtain a layout scheme that not only agrees with the actual site conditions but also attains a high detection probability, short detection time and strong reliability.     

Modeling the chemical and toxic water status of the Scheldt basin (Belgium), using aquatic invertebrate assemblages and an advanced modeling method

Self-Organizing Maps have been used on monitoring sites in several Scheldt sub-basins to identify the main aquatic invertebrate assemblages and relate them to the physico-chemical and toxic water status. 12 physico-chemical variables and 2 estimates of toxic risk were available for a dataset made up of a total of 489 records. Two of the five defining clusters reflecting a relatively clean environment were composed by very well diversified functional feeding groups and sensitive taxa. The cleanest assemblage was mainly linked to the sites from the Nete sub-basin. The three other clusters were inversely described with a dominance of oligochaetes and deposit feeders as well as a bad water quality.Such an analysis can be used to support ecological status assessment of rivers and thus might be useful for decision-makers in the evaluation of chemical and toxic water status, as required by the EU Water Framework Directive.     

Concentration and chemical speciation for the determination of Cu,Zn, Ni,Pb and Cd from refuse dump soils using the optimized BCR sequential extraction procedure

The optimized BCR sequential extraction procedure (proposed by the Standards, Measurements and Testing Programme (SM&T) of the European Union) was applied to seven topsoil samples from refuse dump sites for the determination of Cu, Zn, Ni, Pb and Cd. The metals were partitioned into four operationally defined chemical fractions: acid extractable, reducible, oxidizable and residual, and analysed using flame atomic absorption spectrophotometry, FAAS. The results were compared with total metal concentrations obtained using HNO₃, HClO₄ and HF digestion procedures. Results for total metal analysis ranged from - 15.55 to 43.45 for Cu, 37.15 to 222.35 for Zn, 5.15 to 12.10 for Ni, 10.30 to 93.05 for Pb and 0.35 to 3.75 for Cd in μgg⁻¹ dry weight. The results of the partitioning study showed that zinc prevailed in the more soluble fractions and was distributed between the acid-extractable (32.4%) and the reducible (40.3%) fractions, whereas Pb was distributed mainly in the reducible fraction. Copper and nickel were predominantly associated with the reducible and residual fractions - 53.4, 33.3 and 51.1, 24.1% respectively. The ranking of the four fractions for the partitioning of cadmium was: reducible > residual > oxidizable > acid extractable. The percentage recovery for all metals when comparing total metal concentration with the fractional sum of the optimized BCR procedure, were of the order: Zn(93%) > Pb(83%) > Cu(78) > Cd > (68%) > Ni(63%).     

Water incubation-induced fluctuating release of heavy metals in two smelter-contaminated soils

The soil moisture regime can affect the release of heavy metals in soil. In the previous studies, slightly polluted soils or artificially contaminated soil samples were considered to investigate the effect of soil moisture. We used highly smelter-contaminated and aged soils to study the release of typical heavy metals(Cu, Zn, Cd and Pb) induced by water incubation in batch experiments with characterization via speciation and X-ray diffraction analyses(XRD). The results show that the leachable concentrations of the heavy metals increased slightly in the first 30 days, decreased drastically between 30 and 90 days, and immobilized relatively constant thereafter. The fluctuation was ascribed to the changes of soil Eh and pH, the reductive dissolution of crystalline iron oxides, the formation of new amorphous iron oxides, the absorption of dissolved organic matter and the precipitation of metal sulfide. Speciation analysis indicated that a proportion of the soil heavy metals was transformed from an exchangeable fraction to a less labile fraction after water incubation. And the presence of a lead iron oxide phase and the peak increasing of zinc sulfide were observed via XRD analyses. Finally, water incubation restrained the release of heavy metals after 180 days of incubation, and reduced the leachability of Cu, Zn, Cd and Pb by as much as 1.61%–7.21% for soil A and 0.43%–3.36% for soil B, respectively. The study findings have implications for the formulation of risk control and management strategies for heavy metals in smelter-contaminated soils.     

熔体在岩石形变中的作用综述──来自实验岩石学的证据

实验岩石学的研究表明,岩石中熔体的出现．可诱发断层作用,加强碎裂流动、位错蠕变和扩散蠕变作用。在给定的条件下,上述四种变形机制在部分熔融岩石中都会起作用,但只有那种能产生最快应变速率的机制占主导地位。而应变速率与岩石中熔体的百分数（体积）有关,因此,当熔体的百分数不同时,占主导地位的变形机制会有所不同。临界熔体百分数曾被当作反映部分熔融岩石流变学特征的一个重要参数,但近期的研究表明,临界熔体百分数受诸多因素的影响,或者说部分熔融岩石根本就不存在这样的植。熔体的出现极大地改变了岩石的流变学特征。     

Anaerobic digestion modeling of the main components of organic fraction of municipal solid waste

The organic fraction of municipal solid waste (OFMSW) is composed of several heterogeneous organic and inorganic wastes. The diversity of composition, the high volatile solid content and the biodegradable material that this waste offers make it quite an interesting option for anaerobic digestion (AD). Depending on the substrate composition, the biological degradation and kinetics of the AD could vary. Biochemical methane potential (BMP) tests are used as a tool to evaluate the methane production of several fractions of OFMSW, in order to study the influence of each fraction in the final mixture. The kinetic parameters of methane curves and the prediction of final productions are studied by different approaches to model equations using linear, exponential, logistic and Gaussian models. The analyses of the fractions indicate that organic substrates such as meat/fish which are in a small proportion in the final mixture, obtain major productivities (291 ± 3 mlCH₄/gVS), however others such as paper (217 ± 5 mlCH₄/gVS) could have their productivity enhanced due to their high VS present in the final mixture. Both the Gomperzt and the first order model fit reasonably with all the fractions, although substrates with lag phase adjust only to the Gompertz model explaining 99% of the experimental results.     

Underestimation of phosphorus fraction change in the supernatant after phosphorus adsorption onto iron oxides and iron oxide–natural organic matter complexes

The phosphorus(P) fraction distribution and formation mechanism in the supernatant after P adsorption onto iron oxides and iron oxide-humic acid(HA) complexes were analyzed using the ultrafiltration method in this study.With an initial P concentration of 20 mg/L(I =0.01 mol/L and pH = 7),it was shown that the colloid(1 kDa-0.45 μm) component of P accounted for 10.6%,11.6%,6.5%,and 4.0%of remaining total P concentration in the supernatant after P adsorption onto ferrihydrite(FH),goethite(GE),ferrihydrite-humic acid complex(FH-HA),goethite-humic acid complex(GE-HA),respectively.The 1 kDa component of P was still the predominant fraction in the supernatant,and underestimated colloidal P accounted for 2.2%,55.1%,45.5%,and 38.7%of P adsorption onto the solid surface of FH,FH-HA,GE and GE-HA,respectively.Thus,the colloid P could not be neglected.Notably,it could be interpreted that Fe~(3+) hydrolysis from the adsorbents followed by the formation of colloidal hydrous ferric oxide aggregates was the main mechanism for the formation of the colloid P in the supernatant.And colloidal adsorbent particles co-existing in the supernatant were another important reason for it.Additionally,dissolve organic matter dissolved from iron oxide-HA complexes could occupy large adsorption sites of colloidal iron causing less colloid P in the supernatant.Ultimately,we believe that the findings can provide a new way to deeply interpret the geochemical cycling of P,even when considering other contaminants such as organic pollutants,heavy metal ions,and arsenate at the sediment/soil-water interface in the real environment.     

Impact of soil organic matter on the distribution of polycyclic aromatic hydrocarbons (PAHs) in soils

The knowledge on the distribution of hydrophobic organic contaminants in soils can provide better understanding for their fate in the environment. In the present study, the n-butanol extraction and humic fractionation were applied to investigate the impact of SOM on the distribution of polycyclic aromatic hydrocarbons (PAHs). The results indicated that 80.5%-94.8% of the target PAHs could be extracted by n-butanol and 63.1%-94.6% of PAHs were associated with fulvic acid (FA). Concentrations of un-extracted PAHs increased significantly with the increasing soil organic matter (SOM), however, such an association was absent for the extractable fractions. The results suggested that the sequestration played a critical role in the accumulation of PAHs in soils. SOM also retarded the diffusion of PAHs into the humin fractions. It implied that sequestration in SOM was critical for PAH distribution in soils, while the properties of PAH compounds also had great influences.     

Distributed generation by energy from waste technology: A life cycle perspective

Municipal Solid Waste in general and its organic fraction in particular is a potential renewable and non-seasonal resource. In this work, a life cycle assessment has been performed to evaluate the environmental impacts of two future scenarios using biogas produced from the organic fraction of municipal solid waste (OFMSW) to supply energy to a group of dwellings, respectively comprising distributed generation using solid oxide fuel cell (SOFC) micro-CHP systems and condensing boilers. The London Borough of Greenwich is taken as the reference case study. The system is designed to assess how much energy demand can be met and what is the best way to use the digestible waste for distributed energy purposes.The system is compared with two alternative scenarios fuelled by natural gas: a reference scenario, where the electricity is supplied by the grid and the heat is supplied from condensing boilers, and a fuel cell micro-CHP system. The results show that, although OFMSW alone can only supply between 1% and 4% of the total energy demand of the Borough, a saving of ∼130 tonnes of CO₂ eq per year per dwelling equipped with micro-CHP is still achievable compared with the reference scenario. This is primarily due to the surplus electricity produced by the fuel cell when the micro-CHP unit is operated to meet the heat demand. Use of biogas to produce heat only is therefore a less desirable option compared with combined heat and power production. Further investigation is required to identify locally available feedstock other than OFMSW in order to increase the proportion of energy demand that can be met in this way.