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131.
132.
133.
It is established that the activity of marmots (the genusMarmota) on the surface is timed to the daylight period. In the Arctic, under conditions of continuous illumination (the polar day),
the diurnal rhythm of black-capped marmotsMarmota camtschatica bungei on the surface has a “daylight” pattern. The main external regulator of the diurnal rhythm is the altitude of the sun above
the horizon. In the cold period, however, the effect of air temperature on animal activity becomes stronger. 相似文献
134.
传统概念的地气测量是指地下上升到地表并扩散到大气空间的天然状态气体 ,如CO2 、CH4 、Rn、Hg、H2 等。近十多年的研究证实地气还包含着新的内涵 ,即地壳岩石以及地表土壤中还存着痕量的金属与非金属气体 ,通过捕集这些气体 ,可以获得更多的深部地质构造、矿床信息。据报导 ,国内外的研究主要是在已知矿床上做的正演研究。本文是在已知隐伏断层构造上方地表 ,试验金属与非金属地气存在的可能性。 相似文献
135.
底泥中重金属毒性的室内孔隙水分析技术 总被引:1,自引:0,他引:1
根据孔隙水中重金属的浓度可以判定底泥中重金属的毒性但获得真正的底泥孔隙水十分困难。本文提供了一套简便易行的室内原状孔隙水取样技术,将碳化硅砂芯埋入底泥,添加表层水并静置90d,通过渗滤获得孔隙水,测定孔隙水中重的浓度,所得结果与微生态系统暴露试验中生物指示的重金属的毒性大小相吻合,与生物积累重金属的浓度显著正相关。 相似文献
136.
聚苯乙烯基硫代磺酸钾树脂的合成及其与卤代烃的反应 总被引:2,自引:2,他引:0
由聚苯乙烯基磺酰氯树脂与硫化氢钾反应制备聚苯乙烯基硫代磺酸钾树脂(I),树脂I与亲电的卤代烃反应,生成聚苯乙烯基硫代磺酸酯树脂(Ⅱ),树脂Ⅱ经过乙硫醇处理,使卤代烃结构部分以不对称二硫醚的形式游离下来,用GC/MS对其结构进行鉴定。从不对称二硫醚的结构可推导出原卤代烃的结构,所制备的聚苯乙烯基硫代磺酸钾树脂的转化效率为1.11mmol·g^-1。 相似文献
137.
生物过滤技术在大气污染控制中的应用 总被引:6,自引:0,他引:6
周琪 《城市环境与城市生态》1998,11(1):17-21
生物过滤是控制大气污染的经济有效技术,具有较好的发展前景。本文介绍了生物过滤技术处理废气的研究,应用历史,现状,和生物过滤理论,分析了工艺的使用范围,设计及运行控制要点,列举了应用的范例。 相似文献
138.
A. A. Olajire E. T. Ayodele F. E. Imeokparia 《Environmental monitoring and assessment》1999,57(2):183-194
Samples of compost-amended soil from waste dumping sites in Lagos Metropolis were extracted with dichloromethane (3 × 20 cm3) and the extract was evaporated at 35 °>C. The residue was extracted with 2,2,4-trimethylpentane, and portions of the solution were applied to a column containing silica gel from which aliphatic and aromatic hydrocarbons were eluted with n-hexane and toluene respectively. Analysis of the n-hexane fraction using gas chromatography showed the presence of a mixture of aliphatic hydrocarbons, ranging from C9 to C25, while ultraviolet analysis of the toluene fraction suggested 1,2-benzanthracene; 2,3-benzphenanthrene, chrysene and pyrene as polyaromatic compounds present in samples analyzed. The crude extracts were highly coloured and viscous. Total extractable organic residues in the 2,2,4-trimethylpentane extracts ranged from 36 to 89 mg g-1 of soil. 相似文献
139.
Samaratunga SS Nishimoto J Tabata M 《Environmental science and pollution research international》2008,15(1):27-30
BACKGROUND, AIMS AND SCOPE: Chromium enters into the aquatic environment as a result of effluent discharge from steel works, electroplating, leather tanning industries and chemical industries. As the Cr(VI) is very harmful to living organisms, it should be quickly removed from the environment when it happens to be contaminated. Therefore, the aim of this laboratory research was to develop a rapid, simple and adaptable solvent extraction system to quantitatively remove Cr(VI) from polluted waters. METHODS: Aqueous salt-solutions containing Cr(VI) as CrO4(2-) at ppm level (4-6 ppm) were prepared. Equal volumes (5 ml) of aqueous and organic (2-PrOH) phases were mixed in a 10 ml centrifuge tube for 15 min, centrifuged and separated. Concentrations of Cr(VI), in both the aqueous and organic phases, were determined by atomic absorption spectrometry. The effects of salt and acid concentrations, and phase-contact time on the extraction of Cr(VI) were investigated. In addition, the extraction of Cr(VI) was assessed in the presence of tetramethylammonium chloride (TMAC) in 2-PrOH phase. Effects of some other metals, (Cd(II), Co(II), Cu(II), Ni(II) and Zn(II)), on the extraction of Cr(VI) were also investigated. RESULTS AND DISCUSSION: The Cr(VI) at ppm level was extracted quantitatively by salting-out the homogeneous system of water and 2-propanol(2-PrOH) using chloride salts, namely CaCl2 or NaCl, under acidic chloride media. The extracted chemical species of Cr(VI) was confirmed to be the CrO3Cl-. The ion-pair complex extracted into the organic phase was rationalized as the solvated ion-pair complex of [2-PrOH2+, CrO3Cl-]. The complex was no longer stable. It implied the reaction between extracted species. Studies revealed that salts and acid directly participated in the formation of the above complex. Use of extracting agents (TMAC) didn't show any significant effect on the extraction of Cr(VI) under high salting-out conditions. There is no significant interference effect on the extraction of Cr(VI) by the presence of other metals. The Cr(VI) in the organic phase was back-extracted using an aqueous ammonia solution (1.6 mol dm(-3)) containing 3 mol dm(-3) NaCl. The extraction mechanism of Cr(VI) is also discussed. CONCLUSIONS: Salting-out of homogeneous mixed solvent of 2-propanol can be employed to extract Cr(VI) quantitatively, as an ion-pair of [2-PrOH2+ * CrO3Cl-] solvated by 2-PrOH molecules. Then, the complex becomes 'solvent-like' and is readily separated into the organic phase. The increase of Cl- ion concentration in the aqueous phase favors the extraction. The 2-PrOH, salts and acid play important roles in the extraction process. There is no need to use an extracting agent at a high salting-out condition. RECOMMENDATIONS AND PERSPECTIVES: Chromium(VI) must be quickly removed before it enters into the natural cycle. As the 2-PrOH is water-miscible in any proportion, ion-pairing between 2-PrOH2+ and CrO3Cl- becomes very fast. As a result, Cr(VI) can easily be extracted. Therefore, the method is recommended as a simple, rapid and adaptable method to quickly separate Cr(VI) from aqueous samples. 相似文献
140.
目的 设计针对L波段射频前端敏感器件的强电磁脉冲防护模块,利用瞬态电压抑制二极管、气体放电管和发夹型微带带通滤波器进行联合仿真设计。方法 瞬态电压抑制二极管具有快速响应时间,气体放电管具有高功率容量,而微带带通滤波器可分离噪声信号,并保留有效信号。通过结合这些器件进行防护设计,可以充分发挥各自优势,提高系统稳定性和强电磁脉冲防护能力。结果 该模块设计工作频段为1.3~ 1.7 GHz,带内插入损耗小于1.5 dB,在70 dBm功率注入的情况下,防护效果可以达到42.5 dB,具有良好的防护效果。结论 通过分析研究不同器件的特性和优化设计,实现了对L波段频谱的防护,具有重要的实用价值和广阔的应用前景。 相似文献