多点泄漏对天然气管道沿线压力的影响研究

为研究不同的多点泄漏工况对管道流动参数的影响,基于流动方程建立数学模型,讨论泄漏后压力下降幅值与泄漏位置、泄漏点数的关系,在室内输气环道采集多点泄漏工况下的压力信号并对理论分析结果进行验证。结果表明:泄漏点的上游和下游压力均减小,越靠近泄漏点压力降越大;2个泄漏点之间压力也下降,越靠近上游泄漏点,压力下降幅度越大;泄漏点距起点越近,泄漏引起的压力降低幅值越大。压力下降的幅值受距离起点最近的泄漏点位置影响最大,且随着泄漏点数的增多而增大。     

油气田含油污泥处理相关标准解析

通过对目前已出台油气田含油污泥处理相关标准的解析,针对标准之间存在着适用范围不一致、检测项目名称及限值不一致、检测方法不统一以及计算基础不统一等,造成油气田环保工作者和管理者认识上的混乱,对含油污泥处理技术的选用和治理市场的管理带来诸多问题。为加快促进油气田含油污泥处理减量化、资源化、无害化技术的发展,建议尽快出台有针对性、普适性强、统一的油气田含油污泥污染控制标准,确保含油污泥处理既科学合理,又经济可行;同时制定针对性强的含油污泥污染物检测方法,检测方法统一、计算公式一致,保证结果真实可靠,具有可比性。     

Catalytic oxidation of CO over Pt/Fe3O4 catalysts: Tuning O2 activation and CO adsorption

• Strong metal-support interaction exists on Pt/Fe₃O₄ catalysts. • Pt metal particles facilitate the formation of oxygen vacancies on Fe₃O₄. • Fe₃O₄ supports enhance the strength of CO adsorption on Pt metal particles. The self-inhibition behavior due to CO poisoning on Pt metal particles strongly impairs the performance of CO oxidation. It is an effective method to use reducible metal oxides for supporting Pt metal particles to avoid self-inhibition and to improve catalytic performance. In this work, we used in situ reductions of chloroplatinic acid on commercial Fe₃O₄ powder to prepare heterogeneous-structured Pt/Fe₃O₄ catalysts in the solution of ethylene glycol. The heterogeneous Pt/Fe₃O₄ catalysts achieved a better catalytic performance of CO oxidation compared with the Fe₃O₄ powder. The temperatures of 50% and 90% CO conversion were achieved above 260°C and 290°C at Pt/Fe₃O₄, respectively. However, they are accomplished on Fe₃O₄ at temperatures higher than 310°C. XRD, XPS, and H₂-TPR results confirmed that the metallic Pt atoms have a strong synergistic interaction with the Fe₃O₄ supports. TGA results and transient DRIFTS results proved that the Pt metal particles facilitate the release of lattice oxygen and the formation of oxygen vacancies on Fe₃O₄. The combined results of O₂-TPD and DRIFTS indicated that the activation step of oxygen molecules at surface oxygen vacancies could potentially be the rate-determining step of the catalytic CO oxidation at Pt/Fe₃O₄ catalysts. The reaction pathway involves a Pt-assisted Mars-van Krevelen (MvK) mechanism.     

In situ hydrothermal fabrication of visible light-driven g-C3N4/SrTiO3 composite for photocatalytic degradation of TC

Environmental Science and Pollution Research - A series of g-C3N4/SrTiO3 (CN/SrTiO3) composites with the different mass ratio of g-C3N4 were prepared by facile in situ hydrothermal growth method,...     

Effects of rainfall on surface environment and morphological characteristics in the Loess Plateau

Environmental Science and Pollution Research - Slope failure is a one of major process that causes severe landform variation and environment variation, and slope failure has become a major hidden...     

底泥性质对重金属生物淋滤效果的影响

生物淋滤技术是一项可以将重金属从污染底泥或土壤中分离出来的环境修复技术,具有反应温和、耗酸少、运行成本较低、去除效率高,以及脱毒后底泥的脱水性能好等优点。然而,底泥成分复杂、流域特异性高,这使得相似的生物淋滤工艺对不同底泥的重金属去除效果不尽相同、淋滤技术的工艺参数标准化难度增加。综述了底泥性质对淋滤反应的3方面影响:底泥中的有机质与酸可挥发性硫化物(AVS)会改变重金属的形态;pH、可还原性硫、水溶性有机物(DOM)会对淋滤功能菌的活性产生影响;底泥粒度和耗酸能力(ACC)也会影响重金属的化学淋出效果。在此基础上提出今后该技术有待开展的研究内容,以期为该技术的进一步推广应用提供理论依据和技术支撑。     

Honeybees (<Emphasis Type="Italic">Apis mellifera</Emphasis>) as a biological barrier for contamination of honey by environmental toxic metals

The aim of the study was to investigate the transfer of toxic metals from honeybee workers (Apis mellifera L.) to bee honey in relation to the ecological state of the environment. The materials of the study consisted of samples of honeybee bodies and varietal honeys taken from the same apiary located in three areas: R1—urbanized (16), R2—ecologically clean (16) and R3—industrialized (15) of south-eastern Poland. The contents of 14 elements in all tested samples, including toxic metals (Cd, Pb, Hg, Al, Ni, Tl) as well as bioelements (K, Mg, Ca, Mn, Fe, Zn, Cu, Se), were analysed by the ICP-OES method with prior microwave mineralization. The concentrations of the majority of the studied elements, excluding aluminum and lead, were significantly higher in bee bodies than in honey samples (P?<?0.05). The pollution of bee bodies by toxic metals was dependent on the environmental cleanliness, and the most pollution was observed in the industrialized area. The bee body was the most effective barrier for Cd and Tl transfer to the honey, while the level of Ni was similar in both tested materials. The Al concentration was significantly higher in honey than bee bodies (14.81?±?24.69 and 6.51?±?5.83 mg kg^?1, respectively), which suggests the possibility of secondary contamination of honey. The greatest sensitivity to heavy metal pollution was observed in honeydew honey compared to nectar honeys (P?<?0.05). It was proved for the first time that bees work as biofilters for toxic metals and prevent honey contamination.     

Prediction of the adsorption capability onto activated carbon of a large data set of chemicals by local lazy regression method

Accurate quantitative structure–property relationship (QSPR) models based on a large data set containing a total of 3483 organic compounds were developed to predict chemicals’ adsorption capability onto activated carbon in gas phrase. Both global multiple linear regression (MLR) method and local lazy regression (LLR) method were used to develop QSPR models. The results proved that LLR has prediction accuracy 10% higher than that of MLR model. By applying LLR method we can predict the test set (787 compounds) with Q²_ext of 0.900 and root mean square error (RMSE) of 0.129. The accurate model based on this large data set could be useful to predict adsorption property of new compounds since such model covers a highly diverse structural space.     

Using Si depletion in aerosol to identify the sources of crustal dust in two Chinese megacities

Depletion of Si in transported dust has been recognized for many years. It can be used to distinguish between transported and local dust in cities, although it rarely has been. Here we use the variations of the Si/Al ratio in 15 months of continuous PM_2.5 samples at Beijing (northern China) and Chongqing (southwestern China) to reveal the seasonal patterns of their dust sources. For both cities, peaks of concentration for Si and Al in PM_2.5 corresponded with minima of Si/Al, and could often be linked to pulsed air flow from deserts to the northwest. With significant depletion (up to 80%) and homogeneous distribution at urban and rural sites, Si/Al showed a clear seasonal evolution, which decreased from spring to summer, increased from fall to winter, and collapsed during Chinese Spring Festival, indicating the dominance of transported dust, local fugitive dust and firework influence, respectively. The low ratios implied that desert dust is a common source during spring at Chongqing, whereas its presence during cold season at Beijing was also more frequent than expected. Failing to recognize the depletion of Si may lead to an overestimate of desert dust by 15%–65% when using the average abundance of Al in crust (6%–8%), as in previous studies. The difference in Si/Al ratio between local and transported dust implies that >60% of the dust at Beijing came from outside the city during the springs of 2004–2006. This result can help resolve the contradictory findings on this topic that have been presented earlier.     

Degradation kinetics of anthracene by ozone on mineral oxides

To further understand the role of substrates on the heterogeneous reactions of polycyclic aromatic hydrocarbons, the reactions of ozone with anthracene adsorbed on different mineral oxides (SiO₂, α-Al₂O₃ and α-Fe₂O₃) and on Teflon disc were investigated in dark at 20 °C. No reaction between ozone and anthracene on Teflon disc was observed when the ozone concentration was ～1.18 × 10¹⁴ molecules cm^?3. The reactions on mineral oxides exhibited pseudo-first-order kinetics for anthracene loss, and the pseudo-first-order rate constant (k_1,obs) displayed a Langmuir–Hinshelwood dependence on the gas-phase ozone concentration. The adsorption equilibrium constants for ozone (K_O3) on SiO₂-1, SiO₂-2, α-Al₂O₃ and α-Fe₂O₃ were (0.81 ± 0.26) × 10^?15 cm³, (2.83 ± 1.17) × 10^?15 cm³, (2.48 ± 0.77) × 10^?15 cm³ and (1.66 ± 0.45) × 10^?15 cm³, respectively; and the maximum pseudo-first-order rate constant (k_1,max) on these oxides were (0.385 ± 0.058) s^?1, (0.101 ± 0.0138) s^?1, (0.0676 ± 0.0086) s^?1 and (0.0457 ± 0.004) s^?1, respectively. Anthraquinone was identified as the main surface product of anthracene reacted with ozone. Comparison with previous research and the results obtained in this study suggest that the reactivity of anthracene with ozone and the lifetimes of anthracene adsorbed on mineral dust in the atmosphere are determined by the nature of the substrate.