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191.
A biomass-generated soot was sequentially treated by HCl-HF solution, organic solvent, and oxidative acid to remove ash, extractable native organic matter (EOM), and amorphous carbon. The compositional heterogeneity and nano-structure of the untreated and treated soot samples were characterized by elemental analysis, thermal gravimetric analysis, BET-N2 surface area, and electron microscopic analysis. Sorption properties of polar and nonpolar organic pollutants onto the soot samples were compared, and individual contributions of adsorption and absorption were quantified. The sorption isotherms for raw sample were practically linear, while were nonlinear for the pretreated-soot. The removal of EOM enhanced adsorption and reduced absorption, indicating that EOM served as a partitioning phase and simultaneously masked the adsorptive sites. By drastic-oxidation, the outer amorphous carbon and the inner disordered core of the soot particles were completely removed, and a fullerene-like nanoporous structure (aromatic shell) was created, which promoted additional π-π interaction between phenanthrene and the soot. 相似文献
192.
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194.
垂直流人工湿地水力学特性研究 总被引:6,自引:2,他引:4
通过示踪剂实验从停留时间分布(RTD)曲线及其统计特征值等方面对垂直流人工湿地的水力学特性进行了定性和定量的分析。研究表明水流在垂直流人工湿地中的流动是一种非理想的不均匀流动,存在一定的死区和水流的扩散;垂直流人工湿地较大的死区率与其表面布水的不均匀性有关,这也可能是其死区率大于表流人工湿地的最主要的原因。实验还表明,进水流量对垂直流人工湿地停留时间分布影响较大,随着进水流量的增加,平均停留时间减小,但标准平均停留时间增大,死区率减小;当进水流量为15L/h(水力负荷为620mm/d)时,水流在湿地中的散度最大,水流更接近全混流,不利于污染物的降解。 相似文献
195.
城市轨道交通噪声的声源特性研究进展 总被引:1,自引:0,他引:1
分析了城市轨道交通噪声的主要类型、基本特性、传播规律及其影响因素;综述了国内外城市轨道交通噪声的预测及测量分析技术的研究成果,并对其进行了总结比较,阐述了各种方法的特点、主要成就和局限;最后探讨了城市轨道交通噪声领域今后的研究方向和发展趋势,为解决城市轨道交通发展中的噪声问题提供了参考. 相似文献
196.
强化生物通风修复过程中柴油衰减规律及其影响因素研究 总被引:1,自引:0,他引:1
强化生物通风技术对于修复因地下储油罐泄漏引起的土壤污染具有很大的应用前景。通过室内土柱模拟柴油泄漏污染土壤,从土柱中总石油烃(total petroleum hydrocarbon,TPH)剖面分布随时间的变化及降解模式角度,分析了其自然衰减和强化生物通风过程。结果表明:初始柴油浓度直接影响着各柱在自然衰减和强化生物通风过程中柱内的残余TPH平衡分布曲线的形状和浓度峰值位置;在前期自然衰减过程中(约1个月),当土壤中的柴油浓度为5 000~40 000 mg油/kg土时,整个柱内TPH变化的主要原因是重力扩散迁移的结果;当土壤中的柴油浓度≤5 000 mg油/kg土时,其TPH的变化不仅是重力扩散迁移作用的结果,生物降解作用也存在;通风约2个月后,抽提作用对于保持土柱上部柴油浓度稳定变化的意义较为突出。 相似文献
197.
地铁运行引起的地面振动实测及传播规律分析 总被引:6,自引:0,他引:6
对地铁线路某区间段的地面振动进行实测,采集不同测线和不同测点处的水平方向、竖直方向加速度,并转化为傅里叶幅值谱对其进行衰减规律分析。利用公式将加速度记录换算为振级和分频振级,参照相关的国家标准分析不同距离处的振级和频率成分。对比同一加速度记录中的两对开方向列车引起的地面振动,进一步分析振动衰减的规律。所得到的结果可供地面建筑的隔振减振及城市轨道的规划和设计参考。 相似文献
198.
长江口及其邻近海域表层沉积物分布特征 总被引:4,自引:0,他引:4
根据长江口和杭州湾北部沉积物粒度分析数据,研究表层沉积物类型、分布以及分区特征。结果表明:沉积物的分布特征受水动力条件、地貌类型以及泥沙来源等因素的综合影响,长江口表层沉积物在纵向分布上,自西向东粒径从粗到细、分选程度从好至差,在横向上自北港-北槽-南槽,沉积物粒度逐渐变细;水流动力作用强的河槽和波浪作用强的口门浅滩沉积物粒度较粗,水动力较弱的河口边滩及口外海滨区沉积物则较细。根据沉积物分布特征可将长江口及其邻近海域分为河口分汊河段沉积区、河口拦门沙沉积区、口外海滨沉积区和杭州湾北部沉积区等4个沉积区。 相似文献
199.
Nadeem W. Shah Steven F. Thornton Simon H. Bottrell Michael J. Spence 《Journal of contaminant hydrology》2009,103(3-4):119-133
The potential for aerobic biodegradation of MTBE in a fractured chalk aquifer is assessed in microcosm experiments over 450 days, under in situ conditions for a groundwater temperature of 10 °C, MTBE concentration between 0.1 and 1.0 mg/L and dissolved O2 concentration between 2 and 10 mg/L. Following a lag period of up to 120 days, MTBE was biodegraded in uncontaminated aquifer microcosms at concentrations up to 1.2 mg/L, demonstrating that the aquifer has an intrinsic potential to biodegrade MTBE aerobically. The MTBE biodegradation rate increased three-fold from a mean of 6.6 ± 1.6 μg/L/day in uncontaminated aquifer microcosms for subsequent additions of MTBE, suggesting an increasing biodegradation capability, due to microbial cell growth and increased biomass after repeated exposure to MTBE. In contaminated aquifer microcosms which also contained TAME, MTBE biodegradation occurred after a shorter lag of 15 or 33 days and MTBE biodegradation rates were higher (max. 27.5 μg/L/day), probably resulting from an acclimated microbial population due to previous exposure to MTBE in situ. The initial MTBE concentration did not affect the lag period but the biodegradation rate increased with the initial MTBE concentration, indicating that there was no inhibition of MTBE biodegradation related to MTBE concentration up to 1.2 mg/L. No minimum substrate concentration for MTBE biodegradation was observed, indicating that in the presence of dissolved O2 (and absence of inhibitory factors) MTBE biodegradation would occur in the aquifer at MTBE concentrations (ca. 0.1 mg/L) found at the front of the ether oxygenate plume. MTBE biodegradation occurred with concomitant O2 consumption but no other electron acceptor utilisation, indicating biodegradation by aerobic processes only. However, O2 consumption was less than the stoichiometric requirement for complete MTBE mineralization, suggesting that only partial biodegradation of MTBE to intermediate organic metabolites occurred. The availability of dissolved O2 did not affect MTBE biodegradation significantly, with similar MTBE biodegradation behaviour and rates down to ca. 0.7 mg/L dissolved O2 concentration. The results indicate that aerobic MTBE biodegradation could be significant in the plume fringe, during mixing of the contaminant plume and uncontaminated groundwater and that, relative to the plume migration, aerobic biodegradation is important for MTBE attenuation. Moreover, should the groundwater dissolved O2 concentration fall to zero such that MTBE biodegradation was inhibited, an engineered approach to enhance in situ bioremediation could supply O2 at relatively low levels (e.g. 2–3 mg/L) to effectively stimulate MTBE biodegradation, which has significant practical advantages. The study shows that aerobic MTBE biodegradation can occur at environmentally significant rates in this aquifer, and that long-term microcosm experiments (100s days) may be necessary to correctly interpret contaminant biodegradation potential in aquifers to support site management decisions. 相似文献
200.
David W. Ostendorf Baoshan Xing Niki Kallergis 《Journal of contaminant hydrology》2009,106(3-4):118-130
At a former wood preservation plant severely contaminated with coal tar oil, in situ bulk attenuation and biodegradation rate constants for several monoaromatic (BTEX) and polyaromatic hydrocarbons (PAH) were determined using (1) classical first order decay models, (2) Michaelis–Menten degradation kinetics (MM), and (3) stable carbon isotopes, for o-xylene and naphthalene. The first order bulk attenuation rate constant for o-xylene was calculated to be 0.0025 d− 1 and a novel stable isotope-based first order model, which also accounted for the respective redox conditions, resulted in a slightly smaller biodegradation rate constant of 0.0019 d− 1. Based on MM-kinetics, the o-xylene concentration decreased with a maximum rate of kmax = 0.1 µg/L/d. The bulk attenuation rate constant of naphthalene retrieved from the classical first order decay model was 0.0038 d− 1. The stable isotope-based biodegradation rate constant of 0.0027 d− 1 was smaller in the reduced zone, while residual naphthalene in the oxic part of the plume further downgradient was degraded at a higher rate of 0.0038 d− 1. With MM-kinetics a maximum degradation rate of kmax = 12 µg/L/d was determined. Although best fits were obtained by MM-kinetics, we consider the carbon stable isotope-based approach more appropriate as it is specific for biodegradation (not overall attenuation) and at the same time accounts for the dominant electron-accepting process. For o-xylene a field based isotope enrichment factor εfield of − 1.4 could be determined using the Rayleigh model, which closely matched values from laboratory studies of o-xylene degradation under sulfate-reducing conditions. 相似文献