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191.
为解决低C/N污水的脱氮问题,本实验自行研制开发了一种新型碳聚合物载体.对该载体进行低C/N污水的生物膜脱氮研究,考察了HRT、pH、DO、温度等因素对系统同步硝化反硝化脱氮效果的影响.结果表明:在C/N比为4、pH=8、DO=1 mg/L、HRT=6 h,T=24℃的条件下,氨氮及总氮的去除率分别可以达到90%和70...  相似文献   
192.
采用GC/MS方法对某苯板厂火灾后产生的固体废弃物进行检测分析.结果表明,在苯板火灾后产生的固体废弃物中检测出61种化合物,其中被美国EPA列入优先污染物的苯系物、萘和蒽等占总有机物12.2%.  相似文献   
193.
水中总氮测定相关问题的实验探讨   总被引:1,自引:0,他引:1  
通过对国家标准测定方法《碱性过硫酸钾消解紫外分光光度法》进行水样中总氮的测定,进一步理解在220nm、275nm波长处进行吸光度测定的重要性。并提出:在已经知道水样中没有氨氮、亚硝酸盐氮,只有硝酸盐氮的情况下.就能通过快速的方法一即不加氧化剂、不加压,可以进行总无机氮的测定。快速测定无机总氮对于工程应用来说很有意义。因为国标的方法需要半天时间测定。而用此方法则仅需几分钟就可完成测定。、另外对于有机物对于测定结果的影响,参考吸光度比值(A275/A220×100%)应小于20%,越小越好,超过时应予鉴别。  相似文献   
194.
采用超滤膜法将2-丁烯醛生产废水中的有机物分为相对分子质量不同的7个级分,并应用溶解性有机碳(dissolved organic carbon,DOC)、紫外吸收光谱(ultraviolet spectrum,UV)、傅里叶变换红外光谱(fourier transform infrared spectrometer,FT-IR)和气相色谱/质谱联用仪(gas chromatography with mass spectrometry,GC-MS)技术对不同相对分子质量区间的有机物所占比例及物质结构进行了研究.结果表明,废水中相对分子质量1×103的有机物所占比例最高,达到88.57%;采用GCMS对废水中相对分子质量1×103的级分进行分析,定性出27种化合物,包含醛、酮、酯、醇、酚、酸、烷烃类及其他苯系物等,其峰面积占有机物峰面积总和的比例分别为6.9%、5.3%、35.4%、13.2%、4.6%、0.4%、1.7%、16.8%,总和为84%.UV和FT-IR分析结果均显示不同相对分子质量区间的光谱吸收特征没有明显差别,级分中存在含有不饱和双键、羟基、羰基化合物及芳香族化合物,与GC-MS检测结果相吻合.研究结果为废水处理工艺的开发与优化提供了重要的指导作用.  相似文献   
195.
Catalytic oxidation is widely used in pollution control technology to remove volatile organic compounds. In this study, Pd/ZSM-5 catalysts with different Pd contents and acidic sites were prepared via the impregnation method. All the catalysts were characterized by means of N2 adsorption- desorption, X-ray fluorescence (XRF), HE temperature programmed reduction (H2-TPR), and NH3 temperature programmed desorption (NH3-TPD). Their catalytic performance was investigated in the oxidation of butyl acetate experiments. The by-products of the reaction were collected in thermal desorption tubes and identified by gas chromatography/mass spectrometry. It was found that the increase of Pd content slightly changed the catalytic activity of butyl acetate oxidation according to the yield of CO2 achieved at 90%, but decreased the cracking by-products, whereas the enhancement of strong acidity over Pd-based catalysts enriched the by-product species. The butyl acetate oxidation process involves a series of reaction steps including protolysis, dehydrogenation, dehydration, cracking, and isomerization. Generally, butyl acetate was cracked to acetic acid and 2- methylpropene and the latter was an intermediate of the other by-products, and the oxidation routes of typical by-products were proposed. Trace amounts of 3-methylpentane, hexane, 2-methylpentane, pentane, and 2-methylbutane originated from iso4merization and protolysis reactions.  相似文献   
196.
Titanium dioxide(TiO2), which is the widely used photo-catalyst, has been synthesized by simple hydrothermal solution containing tetrabutyl titanate and hydrofluoric acid. The synthesized product has been applied to photo-degradation in aqueous phase of chlorinated solvents, namely tetrachloroethene(PCE), trichloroethene(TCE) and 1,1,1-trichloroethane(TCA). The photo-degradation results revealed that the degradation of these harmful chemicals was better in UV/synthesized TiO2 system compared to UV/commercial P25 system and UV only system. The photo-catalytic efficiency of the synthesized TiO2 was 1.4, 1.8 and 3.0 folds higher compared to the commercial P25 for TCA, TCE and PCE degradation, respectively. Moreover, using nitrobenzene(NB) as a probe of hydroxyl radical(.OH), the degradation rate was better over UV/synthesized TiO2, suggesting the high concentration of.OH generated in UV/synthesized TiO2system. In addition,.OH concentration was confirmed by the strong peak displayed in EPR analysis over UV/synthesized TiO2system. The characterization result using XRD and TEM showed that the synthesized TiO2 was in anatase form and consisted of well-defined sheet-shaped structures having a rectangular outline with a thickness of 4 nm, side length of 50 nm and width of 33 nm and a surface 90.3 m2/g. XPS analysis revealed that ≡Ti-F bond was formed on the surface of the synthesized TiO2. The above results on both photocatalytic activity and the surface analysis demonstrated the good applicability of the synthesized TiO2 nano-sheets for the remediation of chlorinated solvent contaminated groundwater.  相似文献   
197.
Higher concentrations of Hg can be emitted from coal pyrolysis or gasification than from coal combustion, especially elemental Hg. Highly efficient Hg removal technology from coal-derived fuel gas is thus of great importance. Based on the very excellent Hg removal ability of Pd and the high adsorption abilities of activated carbon(AC) for H2 S and Hg, a series of Pd/AC sorbents was prepared by using pore volume impregnation, and their performance in capturing Hg and H2 S from coal-derived fuel gas was investigated using a laboratory-scale fixed-bed reactor. The effects of loading amount, reaction temperature and reaction atmosphere on Hg removal from coal-derived fuel gas were studied. The sorbents were characterized by N2 adsorption, X-ray diffraction(XRD) and X-ray photoelectron spectroscopy(XPS). The results indicated that the efficiency of Hg removal increased with the increasing of Pd loading amount, but the effective utilization rate of the active component Pd decreased significantly at the same time. High temperature had a negative influence on the Hg removal. The efficiency of Hg removal in the N2-H2S-H2-CO-Hg atmosphere(simulated coal gas) was higher than that in N2-H2S-Hg and N2-Hg atmospheres, which showed that H2 and CO, with their reducing capacity, could benefit promote the removal of Hg. The XPS results suggested that there were two different ways of capturing Hg over sorbents in N2-H2S-Hg and N2-Hg atmospheres.  相似文献   
198.
采用了等体积浸渍法制备二氧化钛负载钒氧化物催化剂(V2O5/TiO2),研究了V2O5负载量、反应温度、烟气流量、氨氮比以及运行时间各因素对NH3选择性催化还原NO反应(SCR)效率的影响.研究结果表明:经过500℃温度下煅烧,烟气流量为200ml/min,负载量为7wt%的V2O5/TiO2催化剂,在400℃温度下反应,NO脱除率可达70.5%.  相似文献   
199.
通过对丽水、宁波、衢州、诸暨等浙江省境内十几个地区的污水处理厂的调查发现:目前浙江省内的污水处理工艺中,A2/O、A/O、氧化沟三种工艺占了近50%的份额。而SBR因其方法特点正在受到越来越多的重视。在污泥处理工艺中,填埋占了最大的一部分,有近70%的污水处理厂将产生的污泥进行填埋处理。目前,污泥处理技术单一,需要继续探寻污泥的减量和资源化技术,为日益增多的污泥探寻出路。  相似文献   
200.
CMC废水属于高盐分高有机物废水,废水COD为50 000~80 000 mg/L,含盐量为13%左右,不适合直接生化处理。本文采用CMC废水和循环冷却水按一定比例混合后一起处理,混合后的废水采用UASB+接触氧化法的处理工艺处理。工程运行表明:稀释后的CMC废水中的盐分稳定在1.4%以内,该处理工艺能够确保出水达到《污水综合排放标准》(GB8978-1996)中三级排放标准。  相似文献   
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