钱塘江杭州段沉积物中铁锰的分布特征

针对钱塘江杭州段水污染现状,对钱塘江杭州段12个采样断面的沉积物进行了系统研究。结果表明,沉积物Fe、Mn的平均含量分别为2.05%,449 mg/kg,变异系数分别为16%、27%。主成分分析结果表明,Fe、Mn、K具有一定的同源性,代表沉积物的自然来源,Fe、Al的分布情况反映两者之间可能存在一定的同源性。相关性分析结果表明,Fe、Al、K均与粘粒显著或极显著相关,反映了地球化学作用和水文条件相互作用的结果;Mn与有机污染(OM)呈显著负相关,说明Mn的污染源与OM不存在同源性,相反,有机质污染导致沉积物锰含量有所降低,两者可能存在密切关系。     

膨胀石墨污水净化处理研究

利用膨胀石墨强大的吸附能力来处理城市生活污水,结果发现用膨胀石墨处理污水的前8h,COD的去除率达43％;处理第5～9d将出现第二个高峰,COD的去除率达48％,分析原因可能是存在物理吸附和微生物絮凝两方面的作用。最后经过20d的处理,膨胀石墨对生活污水的COD和BOD总去除率分别达到86％、78．9％,且除臭能力也很显著。     

化工建设规划生态环境影响评价研究

规划环境影响评价是以可持续发展的思想为出发点,通过调整规划布局或规模从规划源头预防环境污染和生态破坏.文章探讨了化工建设规划的生态环境影响评价理论和方法学体系,并以武汉化工新城为例,对该理论方法体系进行探讨.     

基于均匀分布的滑坡数值模拟参数取值概率研究--以甘肃黑方台黄土滑坡为例

针对数值模拟参数选取主观性强、量化难度大的问题,在高精度无人机地形数据的基础上,通过对11起滑坡案例进行了407组参数反演实验,对结果准确度定量评价后,得到基于Massflow数值软件关键参数λ0的分布范围,进而运用小样本极大似然估计理论,分析区间边界长度对反演精度的影响,最终提出基于均匀分布的参数取值概率模型,并选用案例验证该模型的准确性。结果表明:地形约束会导致反演过程中所需的内聚力减小,反演获得的11组最优λ0的极差和方差分别为0.29、0.01,在置信度为95%下,极大似然法得到区间边界估计长度仅为0.0998,表明参数λ收敛性较好;反演过程中质心滑动距离ψ准确度优于堆积面积重叠率η,在λ0±0.05的范围,参数估计区间内任意值对模拟误差影响较小,评价指标ψ、η与λ0对应案例的相对误差不超过15%;所选案例验证了在置信度为95%下,以反演得到的最优参数区间边界中点构建概率分布函数的可行性和准确性,研究方法可为单体滑坡数值模拟风险评价提供理论支撑。     

Effects of metal and acidic sites on the reaction by-products of butyl acetate oxidation over palladium-based catalysts

Catalytic oxidation is widely used in pollution control technology to remove volatile organic compounds. In this study, Pd/ZSM-5 catalysts with different Pd contents and acidic sites were prepared via the impregnation method. All the catalysts were characterized by means of N2 adsorption- desorption, X-ray fluorescence （XRF）, HE temperature programmed reduction （H2-TPR）, and NH3 temperature programmed desorption （NH3-TPD）. Their catalytic performance was investigated in the oxidation of butyl acetate experiments. The by-products of the reaction were collected in thermal desorption tubes and identified by gas chromatography/mass spectrometry. It was found that the increase of Pd content slightly changed the catalytic activity of butyl acetate oxidation according to the yield of CO2 achieved at 90%, but decreased the cracking by-products, whereas the enhancement of strong acidity over Pd-based catalysts enriched the by-product species. The butyl acetate oxidation process involves a series of reaction steps including protolysis, dehydrogenation, dehydration, cracking, and isomerization. Generally, butyl acetate was cracked to acetic acid and 2- methylpropene and the latter was an intermediate of the other by-products, and the oxidation routes of typical by-products were proposed. Trace amounts of 3-methylpentane, hexane, 2-methylpentane, pentane, and 2-methylbutane originated from iso4merization and protolysis reactions.     

Formation pathways of brominated products from benzophenone-4 chlorination in the presence of bromide ions

The brominated products, formed in chlorination treatment of benzophenone-4 in the presence of bromide ions, were identified, and the formation pathways were proposed.Under disinfection conditions, benzophenone-4 would undertake electrophilic substitution generating mono- or di-halogenated products, which would be oxidized to esters and further hydrolyzed to phenol derivatives. The generated catechol intermediate would be transformed into furan-like heterocyclic product. The product species were p H-dependent,while benzophenone-4 elimination was chlorine dose-dependent. When the chlorination treatment was performed on ambient water spiked with benzophenone-4 and bromide ions, most of brominated byproducts could be detected, and the acute toxicity significantly increased as well.     

Arbuscular mycorrhizal fungal phylogenetic groups differ in affecting host plants along heavy metal levels

Arbuscular mycorrhizal fungi（AMF） are important components of soil microbial communities,and play important role in plant growth. However, the effects of AMF phylogenetic groups（Glomeraceae and non-Glomeraceae） on host plant under various heavy metal levels are not clear. Here we conducted a meta-analysis to compare symbiotic relationship between AMF phylogenetic groups（Glomeraceae and non-Glomeraceae） and host plant functional groups（herbs vs. trees, and non-legumes vs. legumes） at three heavy metal levels. In the meta-analysis, we calculate the effect size（ln（RR）） by taking the natural logarithm of the response ratio of inoculated to non-inoculated shoot biomass from each study. We found that the effect size of Glomeraceae increased, but the effect size of non-Glomeraceae decreased under high level of heavy metal compared to low level. According to the effect size, both Glomeraceae and non-Glomeraceae promoted host plant growth, but had different effects under various heavy metal levels. Glomeraceae provided more benefit to host plants than non-Glomeraceae did under heavy metal condition, while non-Glomeraceae provided more benefit to host plants than Glomeraceae did under no heavy metal. AMF phylogenetic groups also differed in promoting plant functional groups under various heavy metal levels.Interacting with Glomeraceae, herbs and legumes grew better than trees and non-legumes did under high heavy metal level, while trees and legumes grew better than herbs and non-legumes did under medium heavy metal level. Interacting with non-Glomeraceae, herbs and legumes grew better than trees and non-legumes did under no heavy metal. We suggested that the combination of legume with Glomeraceae could be a useful way in the remediation of heavy metal polluted environment.     

Antimony smelting process generating solid wastes and dust：Characterization and leaching behaviors

A large amount of solid waste has been produced by the antimony smelting process in the＂World Capital of Antimony＂, Xikuangshan area in China. This study comprehensively investigated the physical and chemical characteristics of the various solid wastes, as well as the leaching behavior of the solid wastes, which included water-quenched slag,arsenic-alkali residue, desulfurized slag and blast furnace dust. These four types of waste were enriched in a variety of heavy metals and metalloids and more specifically with As and Sb levels up to 8.6 × 104 and 3.16 × 105mg/kg, respectively, in arsenic-alkali residue. For desulfurized slag and water-quenched slag, the leaching concentration of Sb significantly exceeded the acceptable limits during the leaching tests using the toxicity characteristic leaching procedure and the synthetic precipitation leaching procedure. In addition, As leaching in arsenic-alkali residue was extraordinarily hazardous, being three orders of magnitude higher than the regulatory level of As. According to the results of the extraction tests, all the tested wastes were classified as hazardous waste.     

Mo-modified Pd/Al2O3 catalysts for benzene catalytic combustion

Mo-modified Pd/Al2O3catalysts were prepared by an impregnation method and tested for the catalytic combustion of benzene. The catalysts were characterized by N2 isothermal adsorption, X-ray diffraction（XRD）, X-ray photoelectron spectroscopy（XPS）, temperatureprogrammed desorption of NH3（NH3-TPD）, H2temperature-programmed reduction（H2-TPR）, and high-angle annular dark-field scanning transmission electron microscopy（HAADF-STEM）. The results showed that the addition of Mo effectively improved the activity and stability of the Pd/Al2O3catalyst by increasing the dispersion of Pd active components, changing the partial oxidation state of palladium and increasing the oxygen species concentration on the surface of catalyst. In the case of the Pd-Mo/Al2O3catalyst,benzene conversion of 90% was obtained at temperatures as low as 190°C, which was 45°C lower than that for similar performance with the Pd/Al2O3catalyst. Moreover, the 1.0% Pd-5% Mo/Al2O3catalyst was more active than the 2.0% Pd/Al2O3catalyst. It was concluded that Pd and Mo have a synergistic effect in benzene catalytic combustion.     

Photocatalytic activity of Fe-doped CaTiO3 under UV-visible light

The photocatalytic degradation of methylene blue（MB） over Fe-doped CaTiO3 under UV-visible light was investigated. The as-prepared samples were characterized using X-ray diffraction（XRD）, scanning electron microscope（SEM） equipped with an energy dispersive spectrometer（EDS） system, Fourier transform infrared spectra（FT-IR）, and UV-visible diffuse reflectance spectroscopy（DRS）. The results show that the doping with Fe significantly promoted the light absorption ability of CaTiO3 in the visible light region. The Fe-doped CaTiO3 exhibited higher photocatalytic activity than CaTiO3 for the degradation of MB.However, the photocatalytic activity of the Fe-doped CaTiO3 was greatly influenced by the calcination temperature during the preparation process. The Fe-doped CaTiO3 prepared at500°C exhibited the best photocatalytic activity, with degradation of almost 100% MB（10 ppm）under UV-visible light for 180 min.