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91.
以3类常用的碳源(乙酸钠、葡萄糖和甲醇)为研究对象,在3个稳定运行的SBR系统内考察了碳源种类对污水生物脱氮过程中N_2O释放的影响。结果显示,各系统内N_2O的释放主要发生在好氧硝化阶段,且在以乙酸钠为碳源的系统内氨氧化速率最快,TN去除率最大,但同时N_2O的释放速率、累积释放量(4.44 mg)和转化率(1.3%)也最大。而以甲醇为碳源的小试系统脱氮效果较差,TN去除率仅为59.5%,但N_2O的释放速率、累积释放量和转化率均最低。在实际污水处理过程中,当以温室气体N_2O释放作为判断标准时,此研究结果可为碳源的选择提供依据。  相似文献   
92.
本文针对传统基于时差的声发射定位方法精度及稳定性不足且易受检测环境影响的问题,提出了一种基于收敛算法的声发射源定位方法,经过循环迭代不断优化声发射信号的到达时刻计算方式,使得定位计算重构的定位源稳定收敛在近似同一区域,从而提高声发射源的定位准确度。  相似文献   
93.
The acoustic behaviour of Eptesicus serotinus was investigated in the field using a 13.5-m vertical, linear microphone array that allowed for simultaneous recordings at three different heights and for the calculation of flight altitude and distance from the array. Recordings were made at two locations that differed in bat species diversity. E. serotinus hunted on average at an altitude of 10.7 m (±2.7) at one location and 6.8 m (±3.6) at the other location. Search signals were 5–17 ms long depending on flight altitude, and consisted of two to three frequency-modulated harmonics. For bats flying below 8–10 m altitude, signal duration decreased with decreasing flight altitude, whereas signal interval, terminal frequency, peak frequency and frequency range of the first harmonic increased. Above 8–10 m flight altitude, the signal parameters were fairly constant. The –10 dB bandwidth and duty cycle did not change with flight altitude. Source levels were calculated to between 121 and 125 dB peSPL re 20 μPa at 10 cm. For bats flying higher than 9 m, the microphone placed 1.5 m above the ground recorded significantly reduced signal durations and frequency ranges of the first harmonic compared to the same signals recorded with the microphones at heights of 7 or 15 m. We caution the use of ground recordings to fully describe the echolocation signals of high-flying bats. We demonstrate that flight altitude significantly influences the structure of sonar signals from E. serotinus. Received: 17 May 1999 / Received in revised form: 20 September 1999 / Accepted: 25 September 1999  相似文献   
94.
Particles from ambient air and combustion sources including vehicle emission, coal combustion and biomass burning were collected and chemically pretreated with the purpose of obtaining isolated BC (black carbon) samples. TEM (transmission electron microscopy) results indicate that BC from combustion sources shows various patterns, and airborne BC appears spherical and about 50 nm in diameter with a homogeneous surface and turbostratic structure. The BET (Barrett–Emmett–Teller) results suggest that the surface areas of these BC particles fall in the range of 3–23 m2/g, with a total pore volume of 0.03–0.05 cm3/g and a mean pore diameter of 7–53 nm. The nitrogen adsorption–desorption isotherms are indicative of the accumulation mode and uniform pore size. O2-TPO (temperature programmed oxidation) profiles suggest that the airborne BC oxidation could be classified as the oxidation of amorphous carbon, which falls in the range of 406–490°C with peaks at 418, 423 and 475°C, respectively. Generally, the BC characteristics and source analysis suggest that airborne BC most likely comes from diesel vehicle emission at this site.  相似文献   
95.
为考察氯代硝基苯的共代谢降解过程中,有机碳源类型和电子受体对氯代硝基苯厌氧降解过程的影响,以对氯硝基苯(p-CNB,para-chloronitrobenzene)为目标污染物,通过间歇试验考察了葡萄糖、乙醇、乙酸钠等有机碳源及SO2--4、NO3等竞争性电子受体对厌氧微生物降解对氯硝基苯的影响。结果显示,葡萄糖、乙醇和乙酸钠作为碳源时,菌种获得的还原能力大小依次为:乙醇葡萄糖乙酸钠。SO2-4对菌种降解对氯硝基苯过程不产生竞争性抑制。NO-3对对氯硝基苯降解过程的影响与碳源的量有关,当乙醇-COD为100 mg/L时,硝酸盐产生竞争性抑制,且抑制作用随着NO-3浓度升高而增强;当乙醇-COD为600 mg/L时,硝酸盐对菌种降解对氯硝基苯过程不产生竞争性抑制作用。  相似文献   
96.
Carbonyl compounds are important intermediates in atmospheric photochemistry, but their primary sources are still not understood well. In this work, carbonyls, hydrocarbons, and alkyl nitrates were continuously measured during November 2011 at a rural site in the Yangtze River Delta region of China. Mixing ratios of carbonyls and hydrocarbons showed large fluctuations during the entire measurement. The average level for total measured volatile organic compounds during the pollution episode from 25th to 27th November, 2011 was 91.6 ppb, about 7 times the value for the clean period of 7th–8th, November, 2011. To preliminarily identify toluene sources at this site, the emission ratio of toluene to benzene (T/B) during the pollution episode was determined based on photochemical ages derived from the relationship of alkyl nitrates to their parent alkanes. The calculated T/B was 5.8 ppb/ppb, significantly higher than the values of 0.2–1.7 ppb/ppb for vehicular exhaust and other combustion sources, indicating the dominant influence of industrial emissions on ambient toluene. The contributions of industrial sources to ambient carbonyls were then calculated using a multiple linear regression fit model that used toluene and alkyl nitrates as respective tracers for industrial emission and secondary production. During the pollution episode, 18.5%, 69.0%, and 52.9% of measured formaldehyde, acetaldehyde, and acetone were considered to be attributable to industrial emissions. The emission ratios relative to toluene for formaldehyde, acetaldehyde, and acetone were determined to be 0.10, 0.20 and 0.40 ppb/ppb, respectively. More research on industrial carbonyl emission characteristics is needed to understand carbonyl sources better.  相似文献   
97.
水污染源解析技术与应用研究进展   总被引:1,自引:0,他引:1  
阐述了水污染源解析的概念,将水污染源解析方法归纳总结为基于污染负荷估算的方法、基于污染潜力指数的方法及基于源受体污染物特征的方法 3种类型,并分别概述了各种方法的特点,综述了国内外水污染源解析研究的类型与应用进展。最后指出了我国水污染源解析研究在基础资料、研究对象及方法上存在的问题,提出了未来的研究重点。  相似文献   
98.
对2001~2011年固城湖水环境污染状况评价与时空变化特征分析的基础上,探讨了固城湖的特征污染物及污染来源。结果表明,固城湖水质污染的主要超标因子为TN和TP;总体水质呈现先恶化再改善的趋势,污染由拦河网水域向小湖区水域扩散;固城湖湖体水质基本上劣于水环境功能区划要求;固城湖特征污染物为COD+M n、NH4-N、TN、TP、BOD 5;富营养化程度不断加重,之后又有所改善;氮磷污染的主要来源是水产养殖污染。  相似文献   
99.
Despite increasing attention to management of headwater streams as sources of water, sediment, and wood to downstream rivers, the extent of headwater channels and perennial flow remain poorly known and inaccurately depicted on topographic maps and in digital hydrographic data. This study reports field mapping of channel head and perennial flow initiation locations in forested landscapes underlain by sandstone and basalt lithologies in Washington State, USA. Contributing source areas were delineated for each feature using a digital elevation model (DEM) as well as a Global Positioning System device in the field. Systematic source area–slope relationships described in other landscapes were not evident for channel heads in either lithology. In addition, substantial variability in DEM-derived source area sizes relative to field-delineated source areas indicates that in this area, identification of an area–slope relationship, should one even exist, would be difficult. However, channel heads and stream heads, here defined as the start of perennial flow, appear to be co-located within both of the lithologies, which together with lateral expansion and contraction of surface water around channel heads on a seasonal cycle in the basalt lithology, suggest a controlling influence of bedrock springs for that location. While management strategies for determining locations of channel heads and perennial flow initiation in comparable areas could assign standard source area sizes based on limited field data collection within that landscape, field-mapped source areas that support perennial flow are much smaller than recognized by current Washington State regulations.  相似文献   
100.
In the EU-FP7 project APPRAISAL the current practice for integrated assessment modelling (IAM) of air quality in the EU was reviewed, limitations were identified and guidance for improvements was provided. In this article we present the guidance proposed by APPRAISAL. This guidance takes into account that a single IAM solution does not exist but that the different elements of the IAM methodology can be addressed in more or less detail taking into account the available data, the regional/local specificities, the financial resources and the actual purpose of the assessment.  相似文献   
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