Formation of sulfur oxide groups by SO2 and their roles in mercury adsorption on carbon-based materials

The presence of SO₂ display significant effect on the mercury (Hg) adsorption ability of carbon-based sorbent. Yet the adsorption and oxidation of SO₂ on carbon with oxygen group, as well as the roles of different sulfur oxide groups in Hg adsorption have heretofore been unclear. The formation of sulfur oxide groups by SO₂ and their effects on Hg adsorption on carbon was detailed examined by the density functional theory. The results show that SO₂ can be oxidized into SO₃ by oxygen group on carbon surface. Both C-SO₂ and C-SO₃ can improve Hg adsorption on carbon site, while the promotive effect of C-SO₂ is stronger than C-SO₃. Electron density difference analyses reveal that sulfur oxide groups enhance the charge transfer ability of surface unsaturated carbon atom, thereby improving Hg adsorption. The experimental results confirm that surface active groups formed by SO₂ adsorption is more active for Hg adsorption than the groups generated by SO₃.     

在役储运装置安全控制系统改造要求

基于对国内在役储运装置(大型储油罐区、站场、长输管道)安全控制/管理现状调研分析,并结合国际国内标准IEC61508和IEC61511(GB/T20438和GB/T21109)及国外石油公司良好的工程实践,开展在役储运装置安全控制系统可靠性研究,制定适应于储运装置成套的安全控制方案,形成在役储运装置安全控制系统设置/管理要求。     

Synthesis of a novel ternary HA/Fe-Mn oxides-loaded biochar composite and its application in cadmium(II) and arsenic(V) adsorption

Cadmium (Cd) and arsenic (As) are two of the most toxic elements. However, the chemical behaviors of these two elements are different, making it challenging to utilize a single adsorbent with high adsorption capacity for both Cd(II) and As(V) removal. To solve this problem, we synthesized HA/Fe-Mn oxides-loaded biochar (HFMB), a novel ternary material, to perform this task, wherein scanning electron microscopy (SEM) combined with EDS (SEM-EDS) was used to characterize its morphological and physicochemical properties. The maximum adsorption capacity of HFMB was 67.11?mg/g for Cd(II) and 35.59?mg/g for As(V), which is much higher compared to pristine biochar (11.06?mg/g, 0?mg/g for Cd(II) and As(V), respectively). The adsorption characteristics were investigated by adsorption kinetics and the effects of the ionic strength and pH of solutions. X-ray photoelectron spectroscopy (XPS) and Fourier-transform infrared spectroscopy (FT-IR) revealed that chelation and deposition were the adsorption mechanisms that bound Cd(II) to HFMB, while ligand exchange was the adsorption mechanism that bound As(V).     

Improved activity and durability of Rh-based three-way catalyst under diverse aging atmospheres by ZrO2 support

The catalytic activity and durability of Rh/ZrO_2 catalyst were investigated compared with Rh/Al_2O_3 catalyst under diverse aging atmospheres, including lean, rich and lean–rich cyclic aging atmospheres, to simulate the real working conditions of three-way catalyst.Oxidation states and microstructures of rhodium species were investigated to correlate with the catalytic performance of the catalysts. The catalytic performance and durability of the Rh catalyst under diverse aging atmospheres were drastically enhanced by ZrO_2 support. ZrO_2 support was confirmed to be able to effectively inhibit rhodium sintering even under diverse aging conditions. It can also successfully keep Rh species in an active low-valence state on the surface of the catalyst. The superiority of ZrO_2 support compared to Al_2O_3 was verified by the Rh-based monolith catalyst.     

Chemical characterization and source apportionment of atmospheric submicron particles on the western coast of Taiwan Strait, China

Taiwan Strait is a special channel for subtropical East Asian Monsoon and its western coast is an important economic zone in China. In this study, a suburban site in the city of Xiamen on the western coast of Taiwan Strait was selected for fine aerosol study to improve the understanding of air pollution sources in this region. An Aerodyne high-resolution time-of-flight aerosol mass spectrometer(HR-To F-AMS) and an Aethalometer were deployed to measure fine aerosol composition with a time resolution of 5 min from May 1to 18, 2015. The average mass concentration of PM1 was 46.2 ± 26.3 μg/m~3 for the entire campaign. Organics(28.3%), sulfate(24.9%), and nitrate(20.6%) were the major components in the fine particles, followed by ammonium, black carbon(BC), and chloride. Evolution of nitrate concentration and size distribution indicated that local NOx emissions played a key role in high fine particle pollution in Xiamen. In addition, organic nitrate was found to account for 9.0%–13.8% of the total measured nitrate. Positive Matrix Factorization(PMF)conducted with high-resolution organic mass spectra dataset differentiated the organic aerosol into three components, including a hydrocarbon-like organic aerosol(HOA) and two oxygenated organic aerosols(SV-OOA and LV-OOA), which on average accounted for 27.6%,28.8%, and 43.6% of the total organic mass, respectively. The relationship between the mass concentration of submicron particle species and wind further confirmed that all major fine particle species were influenced by both strong local emissions in the southeastern area of Xiamen and regional transport through the Taiwan Strait.     

PAHs pass through the cell wall and partition into organelles of arbuscular mycorrhizal roots of ryegrass

The subcellular process and distribution of polycyclic aromatic hydrocarbons (PAHs) in arbuscular mycorrhizal plants remains to be elucidated. This work used a greenhouse experiment to show that, accompanied by the apoplastic and symplastic water movement through the root, acenaphthene (ACE) as a representative PAH passed through the cell-wall boundary, dissolved in the cell solution, and partition organelles in arbuscular mycorrhizal roots of ryegrass (Lolium multiflorum Lam.). The observed concentrations of ACE in organelles were 0.6 to 4.4 times higher than in the cell walls. The cell wall and organelles were the dominant storage domains for ACE in the root, and the distribution of ACE in cells of mycorrhizal ryegrass roots was, in descending order, cell organelles (40.8-70.8%) > cell wall (19.7-3.8%) cell solution (9.6-20.5%).     

Ecology of hemiepiphytism in fig species is based on evolutionary correlation of hydraulics and carbon economy

Woody hemiepiphytic species (Hs) are important components of tropical rain forests, and they have been hypothesized to differ from non-hemiepiphytic tree species (NHs) in adaptations relating to water relations and carbon economy; but few studies have been conducted comparing ecophysiological traits between the two growth forms especially in an evolutionary context. Using common-garden plants of the genus Ficus, functional traits related to plant hydraulics and carbon economy were compared for seven NHs and seven Hs in their adult terrestrial "tree-like" growth phase. We used phylogenetically independent contrasts to test the hypothesis that differences in water availability selected for contrasting suites of traits in Hs and NHs, driving evolutionary correlations among functional traits including hydraulic conductivity and photosynthetic traits. Species of the two growth forms differed in functional traits; Hs had substantially lower xylem hydraulic conductivity and stomatal conductance, and higher instantaneous photosynthetic water use efficiency. Leaf morphological and structural traits also differed strikingly between the two growth forms. The Hs had significantly smaller leaves, higher leaf mass per area (LMA), and smaller xylem vessel lumen diameters. Across all the species, hydraulic conductivity was positively correlated with leaf gas exchange indicating high degrees of hydraulic-photosynthetic coordination. More importantly, these correlations were supported by correlations implemented on phylogenetic independent contrasts, suggesting that most trait correlations arose through repeated convergent evolution rather than as a result of chance events in the deep nodes of the lineage. Vatiation in xylem hydraulic conductivity was also centrally associated with a suite of other functional traits related to carbon economy and growth, such as LMA, water use efficiency, leaf nutrient concentration, and photosynthetic nutrient use efficiency, indicating important physiological constraints or trade-offs among functional traits. Shifts in this trait cluster apparently related to the adaptation to drought-prone canopy growth during the early life cycle of Hs and clearly affected ecophysiology of the later terrestrial stage of these species. Evolutionary flexibility in hydraulics and associated traits might be one basis for the hyper-diversification of Ficus species in tropical rain forests.     

任务驱动式教学在高职《环境法学》课程中的应用

在任务驱动教学法下,在自主学习中提出问题、解决问题是重点,进行学习效果评价、形成反馈信息是总结提高阶段,每一个环节都必须统筹安排,合理兼顾。《环境法学》课程教学活动中合理采用任务驱动教学法,不仅充分体现了以学生为主体、老师为主导的现代教育思想,而且极大地调动了学生的积极性和创造性,也为提高学生的实践能力和创新能力营造了良好的氛围。     

Threats to China’s Biodiversity by Contradictions Policy

China has among the highest biodiversities in the world, but faces extreme biodiversity losses due to the country’s huge population and its recent explosive socioeconomic development. Despite huge efforts and investments by the government and Chinese society to conserve biodiversity, especially in recent decades, biodiversity losses may not have been reversed, and may even have been exacerbated by unintended consequences resulting from these projects. China’s centralized approach to biodiversity conservation, with limited local participation, creates an inflexible and inefficient approach because of conflicts between local communities and national administrators over the benefits. Although community-based conservation may be an imperfect approach, it is an essential component of a successful future national conservation plan. Biodiversity conservation should be considered from the perspective of systems engineering and a governance structure that combines centralization with community-level conservation. In this paper, we describe China’s complex challenge: how to manage interactions between humans and nature to find win–win solutions that can ensure long-term biodiversity conservation without sacrificing human concerns.     

聚(苯乙烯-甲基丙烯酸)复合磁性微球的吸附性能

以共沉淀法制备纳米Fe3O4,通过分散聚合法制备了磁性聚(苯乙烯-甲基丙烯酸)(Fe3O4@P(St-MMA))微球,采用光学显微镜、红外光谱、样品磁力振荡计和X射线衍射(XRD)对磁性微球进行了表征。考察了复合磁性微球在不同的p H、离子强度和吸附时间等条件下对其吸附性能的影响,运用吸附动力学和吸附等温线研究了磁性微球对亚甲基蓝的表面吸附机理。结果表明,制备的磁性微球粒径在100~200μm之间,表面含有羧基,饱和磁化强度为9.44 emu/g,在外加磁场的作用下能够快速分离出来。亚甲基蓝的吸附符合准二级动力学模型,在100 min内基本达到吸附平衡;25℃下,最大吸附量高达144.9 mg/g,且吸附随着p H值的升高而增加,当p H7时,吸附量基本不变;随着离子强度增加,吸附量逐渐下降;Langmuir等温线能比较好地拟合磁性微球对溶液中亚甲基蓝的吸附。