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11.
As a remedial option, the natural attenuation capacity of a petroleum contaminated groundwater at a military facility was examined. Hydrogeological conditions, such as high water level, permeable uppermost layer and frequent heavy rainfall, were favorable to natural attenuation at this site. The changes in the concentrations of electron acceptors and donors, as well as the relevant hydrochemical conditions, indicated the occurrence of aerobic respiration, denitrification, iron reduction, manganese reduction and sulfate reduction. The calculated BTEX expressed biodegradation capacity ranged between 20.52 and 33.67 mg/L, which appeared effective for the reduction of the contaminants levels. The contribution of each electron accepting process to the total biodegradation was in the order: denitrification > iron reduction > sulfate reduction > aerobic respiration > manganese reduction. The BTEX and benzene point attenuation rates were 0.0058-0.0064 and 0.0005-0.0032 day-1, respectively, and the remediation time was 0.7-1.2 and 2.5-30 years, respectively. The BTEX and benzene bulk attenuation rates were 8.69 × 10-4 and 1.05 × 10-3 day-1, respectively, and the remediation times for BTEX and benzene were 7.2 and 17.5 years, respectively. However, most of the natural attenuation occurring in this site can be attributed to dilution and dispersion. Consequently, the biodegradation and natural attenuation capacities were good enough to lower the contaminants levels, but their rates appeared to be insufficient to reach the remediation goal within a reasonable time frame. Therefore, some active remedial measures would be required.  相似文献   
12.
为研究管道内金属丝网对甲烷/空气预混火焰传播的影响,通过实验和三维数值模拟研究安装金属丝网的管道内火焰传播特性以及流场、温度场的变化。结果表明:40目4层的金属丝网可以使火焰淬熄,30目4层的金属丝网无法淬熄,但可以使火焰停滞3 ms;大涡模型可以很好地对管道内火焰淬熄现象进行模拟;当火焰穿过30目4层金属丝网时,速度增大,在Kelvin Helmholtz不稳定和Rayleigh Taylor不稳定的耦合作用下形成湍流;金属丝网的目数会影响热量在丝网层中的扩散,当金属丝网为30目4层时,火焰热量扩散快,而当金属丝网为40目4层时,火焰热量扩散慢且温度大幅度衰减,衰减率达到83%。  相似文献   
13.
李吉刚 《环境技术》2006,24(6):31-32
我国正在建设的青藏铁路是世界上海拔最高、线路最长的高原铁路.其气候特点对橡胶制品提出了新的技术要求,为适应在该气候条件下的运用需要,进行了针对空气弹簧胶囊用橡胶的耐紫外线老化试验研究工作,试验表明随着紫外线老化时间的增加,其硬度和300%定伸强度均提高,但拉伸强度和扯断伸长率随着紫外线老化时间的增加而降低;通过与胶料的耐臭氧试验和大气老化试验比较,基本可以认为引起空气弹簧胶囊表面龟裂的主要原因是受力状况、臭氧和大气老化的作用,而紫外线对橡胶的表面龟裂影响作用不大,因此,为提高空气弹簧胶囊的耐老化性能,主要考虑降低橡胶的受力,提高耐臭氧和耐大气老化性能.  相似文献   
14.
选取某城市L型综合管廊电缆舱为研究对象,采用FDS数值模拟软件研究了不同火源位置对L型管廊电缆火灾温度纵向衰减规律、烟气浓度分布规律及烟气危害性的影响。研究结果表明,L型廊道构型影响了不同火源位置的管廊电缆火灾最高温度纵向衰减的连续性,基于热边界层理论提出了适用于L型管廊的二维平面最高温度纵向衰减模型。基于峰宽时间计算了L型管廊火灾的烟气总危害性参数,不同火源位置的烟气危害性总在靠近管廊节点位置处最低。这些结果可对综合管廊的消防设计与火灾防控提供参考。  相似文献   
15.
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   
16.
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   
17.
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   
18.
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   
19.
对强夯施工的现场进行了近距离的测量 ,得到了最大地动位移值随距离的变化特征 ,其衰减规律较好地符合负幂函数衰减规律 ,水平径向与垂直向的衰减指数分别为 1 495 3,0 4714。  相似文献   
20.
This study characterized organic compounds found in New York State manufactured gas plant (MGP) coal tar vapors using controlled laboratory experiments from four separate MGP sites. In addition, a limited number of deep (0.3–1.2 m above coal tar) and shallow (1.2–2.4 m above coal tar) soil vapor samples were collected above the in situ coal tar source at three of these sites. A total of 29 compounds were consistently detected in the laboratory-generated coal tar vapors at 50°C, whereas 24 compounds were detected at 10°C. The compounds detected in the field sample results were inconsistent with the compounds found in the laboratory-generated samples. Concentrations of compounds in the shallow soil vapor sample were either non-detectable or substantially lower than those found in deeper samples, suggesting attenuation in the vadose zone. Laboratory-generated data at 50°C compared the (% non-aromatic)/(% aromatic) ratio and indicated that this ratio may provide good discrimination between coal tar vapor and common petroleum distillates.  相似文献   
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