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31.
研究温压炸药爆炸初期弹内爆炸波作用过程,可以进一步分析温压炸药分散爆轰的作用机理,为温压炸药武器设计和系统优化提供可靠依据.设计了用测时法研究温压炸药爆轰波传播速度的试验装置,并用探针对相同组分和密度条件下、温压战斗部弹内爆炸初期的爆炸作用过程进行了对比试验,记录了触发时间信号,计算并分析了温压炸药弹内爆炸波的传播特性,得到了波阵面与弹径方向夹角α的变化规律.试验结果表明,温压炸药的爆轰波传播速度为4.632km/s,其弹内爆轰波的传播特性与中心高能分散药的爆轰波有密切联系,通过合理设计弹体结构和比药量,可以实现温压炸药的分散爆轰,提高温压炸药的爆炸威力. 相似文献
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采空区遗煤自燃过程及其规律的数值模拟研究 总被引:16,自引:5,他引:16
李宗翔 《中国安全科学学报》2005,15(6):15-19
基于非均质多孔介质中的连续性方程、多相气体渗流———扩散方程和综合传热方程,建立了工作面动态推进下的采空区自燃数值模型。结合实例,从理论上描绘了工作面开采过程中采空区的漏风流态、氧、CO、瓦斯和温度等分布状态及其动态过程。计算中考虑了瓦斯涌出对自燃的耦合作用;工作面动态推进对自燃的影响,以及沿边界冒落非压实性对漏风供氧、自燃高温区产生的影响。从理论上重点讨论了采空区自燃与各因素的定量化关系,得出自然发火期与煤氧化速度、工作面风量二者均呈显著的反比例关系;对于综放工作面采场漏风供氧系统,自然发火期主要取决于煤的耗氧能力,提高工作面风量仅能扩大自燃高温区的范围,增大自燃的发生几率;提高推进度能显著延长采空区自然发火期,呈指数变化。 相似文献
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A new potassium permanganate reagent with slow-release properties was designed and tested for possible application in in situ chemical oxidation. For this purpose, MnO2-coated KMnO4 particles (MCP) were prepared by partial reduction of solid KMnO4 using the acid-catalyzed reaction with n-propanol or the comproportionation of Mn(VII) and Mn(II) in n-propanol as reaction medium. Column tests showed that, for MCP with a residual KMnO4 fraction of 70 wt%, the duration of permanganate release under flow-through conditions was prolonged by a factor of 10 compared to untreated KMnO4. While KMnO4 is too soluble to be used in reactive barriers, MCP could be introduced into the aquifer by filling of trenches or boreholes; this would allow a prolonged passive dosing of permanganate into the flowing groundwater. In addition, experiments were conducted in order to determine the oxidation capability of native KMnO4 particles and MCP in CH2Cl2, a representative non-polar non-aqueous phase liquid (NAPL). It may be possible to utilize the significantly higher reactivity of MCP under these conditions for the design of slow-release permanganate particles for NAPL source treatment. 相似文献
35.
Alexander V. Fedorov Alexey V. Shulgin 《Journal of Loss Prevention in the Process Industries》2007,20(4-6):317-321
The distributed mathematical model of magnesium particle ignition is developed taking into account the heterogeneous chemical reaction and the domain of particle thermal influence on gas. The problem solvability in the stationary case has allowed one to expand classification of regular modes of heating as well as the modes of extinction and ignition of a particle. The limiting size of a gas layer near a particle is found that determines an ignition mode. It is shown that the ignition delay time grows if we take into account the gas layer near the particle. Stability of some heating modes within the framework of finite and infinitesimal perturbations is studied. An opportunity to control the ignition process by high-frequency thermal action on the unstable particle gas states is shown. 相似文献
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An interaction of a detonation wave propagating in the cellular detonation mode with a cloud of inert particles is investigated numerically. The analysis of results allows the regimes of propagation of the heterogeneous plane Chapman–Jouguet and cellular detonations and their suppression to be identified. The influence of various parameters of the inert cloud is demonstrated. The critical length of the cloud sufficient for detonation suppression is determined. It is shown that the disperse composition and the nonuniform distribution of particles in the cloud are important parameters affecting the detonation propagation mode. 相似文献
38.
Zhaoyue Sun Lisha Feng Guodong Fang Longgang Chu Dongmei Zhou Juan Gao 《环境科学学报(英文版)》2021,33(3):248-259
Nano-Fe2O3 embedded in montmorillonite particles (Fe-Mt) were prepared to degrade diethyl phthalate (DEP) with citric acid (CA) under xenon light irradiation. Compared to pristine montmorillonite (Na-Mt), the embedding process increased 14.5-fold of iron content and 1.8-fold of specific surface area. The synthesized Fe-Mt have more oxygen vacancies than Fe2O3 nanoparticles (nFe2O3), which could induce more reactive oxygen species (ROSs) generation in the presence of CA under xenon lamp irradiation. Fe-Mt with CA enhanced photo-assisted degradation of DEP 2.5 times as compared to nFe2O3 with CA. Quenching experiments, electron paramagnetic resonance (EPR) spectroscopy and identification of products confirmed that surface-bound ?OH was the main radical to degrade DEP. Common anions (i.e., NO3?, CO32?, Cl?) and humic acid could compete ?OH with DEP and cause slower degradation of DEP. The removal efficiency of DEP was more than 56% with Fe-Mt after three recycles, and the dissolved Fe concentration from Fe-Mt was below 75 μmol/L, indicating Fe-Mt had a good stability as a catalyst. Fe-Mt together with CA appeared to be a promising strategy to remove organic pollutants in surface water, or topsoil under solar irradiation. 相似文献
39.
A dynamic and heterogeneous species abundance model generating the lognormal species abundance distribution is fitted to time series of species data from an assemblage of stoneflies and mayflies (Plecoptera and Ephemeroptera) of an aquatic insect community collected over a period of 15 years. In each year except one, we analyze 5 parallel samples taken at the same time of the season giving information about the over-dispersion in the sampling relative to the Poisson distribution. Results are derived from a correlation analysis, where the correlation in the bivariate normal distribution of log abundance is used as measurement of similarity between communities. The analysis enables decomposition of the variance of the lognormal species abundance distribution into three components due to heterogeneity among species, stochastic dynamics driven by environmental noise, and over-dispersion in sampling, accounting for 62.9, 30.6 and 6.5% of the total variance, respectively. Corrected for sampling the heterogeneity and stochastic components accordingly account for 67.3 and 32.7% of the among species variance in log abundance. By using this method, it is possible to disentangle the effect of heterogeneity and stochastic dynamics by quantifying these components and correctly remove sampling effects on the observed species abundance distribution. 相似文献
40.
特别选题:环境微界面过程与污染控制序 总被引:1,自引:0,他引:1
长期以来,人们主要关注的是污染物的均相环境过程,这一点在大气污染化学和水污染化学的研究中尤其明显。然而近年来,人们开始关注环境中的非均相反应过程,从相对微观的尺度思考和探索环境的微界面问题,并从不同的视角不断认识和揭示这一过程在环境污染及其控制中的作用和意义。1997年,由荷兰科学家L.K.Koopal教授发起设立了Interfaces Against Pollution两年一次的系列国际会议,形成了全球范围内有关科学研究组织和科学家探讨和交流环境界面问题的重要平台。中国科学院生态环境研究中心汤鸿霄院士在我国首次提出环境微界面的概念,并于2003年主编了《环境科学学报》之“环境微界面过程研究论文专辑”,为该专辑作序并发表了“环境纳米污染物与微界面水质过程”的研究论文,对环境纳米微界面问题给出了全面和准确的内涵,进而开启了我国在此方面的系统性研究工作。基于汤鸿霄院士提出的环境微界面内涵和思想,2006年中国科学院生态环境研究中心组织了“环境微界面过程与污染控制”创新研究群体,得到国家自然科学基金委员会的资助。群体的研究目标是深入探索污染物在环境微界面的转移转化机制与控制原理,力争在复杂条件下微界面的定量化表征、污染物在环境微界面的转移转化规律及复合效应、基于微界面原理的环境过程调控等方面取得科学与技术突破。该研究群体的建立及深入开展相关的研究工作,将有力推动我国环境微界面理论和技术的研究进展,也将不断培养本研究方向的专业化高级人才。在过去的2年里,该研究群体在不同环境微界面特征及过程表达、污染物在典型介质和界面变化行为的原位观测、水/气/土/生物微界面上污染物的转移转化规律、基于微界面过程的水、气、固等环境的污染控制等方面取得预期研究进展。本专栏所组织的稿件,即试图从不同角度反映我们所关注的环境微界面研究领域,并通过前期研究所获得的一些具体的科学数据和结果,对环境微界面过程给出进一步的认识。然而,由于本群体的研究工作还不够深入,这样一个专栏所发表的内容不论是对环境微界面的概念与内涵,还是在探索与创新上,都还是初步的和不成熟的。或者说,本专栏所反映的只是一个有待发展和完善的科学思路。由于本专栏作者水平有限,这些论文定有不少谬误之处,敬请读者批评指正。
衷心感谢《环境科学学报》编辑部为我们提供这样一个重要的平台和机会,感谢他们为本专栏组稿、编辑和出版所做出的辛苦努力! 相似文献