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11.
Most native polymers used in processing and application technologies are admittedly disposable from the environment in a biologic manner, but products possess low mechanical strength. One of the paths to increasing this attribute (if feasible) is their cross-linking, which may, however, affect their readiness to biodegradation. In the presented work this condition was observed on the example of waste protein (Hykol B) cross-linking by means of glutardialdehyde and glyoxal. Degree and course of cross-linking were determined through impedance spectroscopy. The objective of this work also was to obtain data for constructing a sensor capable of following the cross-linking course in real time, for potential industrial application of Hykol in continuous production. Impedance spectroscopy proved to be applicable even to this kind of material marked by considerable water content and exhibiting relatively high electric conductivity; so far it had been used only for materials of low conductivity. An aqueous environment inoculated with digested anaerobic sludge from a municipal wastewater treatment plant was selected for modeling anaerobic conditions. The relation was studied between cross-linking degree given by content of cross-linking agent (determined by impedance spectroscopy) and biodegradation degree under anaerobic conditions. It was confirmed that network density as given by quantity of added agent not only reduced breakdown degree but also slowed the course of the process. This fact is particularly obvious with cross-linking by means of glyoxal; network density is thus dependent on type of employed substance, which affect type and structure of created network. That not merely forms an obstacle during polymer swelling and dissolution but also prevents access of bacteria to source of metabolized organic carbon.  相似文献   
12.
选用0.1μm的PVDF中空纤维内压式微滤膜组件,在死端微滤工况下,研究了酵母(平均粒径5.3μm)和高岭土(平均粒径0.7μm)体系在浓度和压力变化时的污染机理及过滤阻力、膜渗透通量的变化规律性。通过恒压堵塞定律积分式的具体形式与实验数据的拟合及根据堵塞过滤定律计算的结果都表明:死端微滤时,酵母体系和高岭土体系均符合滤饼过滤机理。  相似文献   
13.
The chemistry of high mountain snowpacks is a result of the long-range atmospheric transport and deposition of elements. Pyrenean snowpacks contain information about the fluxes of elements over SW Europe in winter. Here we analysed Al, Ti, Mn, Fe, Ni, Cu, Zn, As, Se, Cd and Pb in the 2004–05 winter snowpack in the Central Pyrenees, at an altitude range of 1820–3200 m a.s.l. Ni, As, Se and Cd were not detected in most cases. The concentrations of the remaining elements were comparable to those found in other high mountain areas in Europe and North America considered representative of regional background of atmospheric deposition in populated areas. In contrast, our measurements were higher than those of polar areas, which represent the global background. Single measurements of concentrations and snow accumulation were subject to considerable spatial variability, which may be attributable to strong wind drift and other post-depositional processes. The major ions chemistry of the snow indicated three possible origins for the solutes: terrigenous dust, sea salt spray and polluting S and N aerosols. We found no association between Cu, Zn and Pb and any of these possible sources. This observation therefore indicates that these elements were not preferentially bound to any particular kind of aerosol. Snow collected at altitudes of up to 2050 m a.s.l. presented higher concentrations of several elements than snow above this altitude, thereby indicating a local influence. Snow collected above 2300 m a.s.l. was therefore more representative of broad regional inputs. At these higher altitudes, snow was not enriched in Al, Ti, Mn, Fe or As compared with the composition of the upper continental crust and the local lithology, and these elements (except Mn) appeared almost exclusively in the particulate fraction. This observation indicates that Al, Ti, Mn, Fe and As were present mainly as part of dust particles of terrigenous origin. In contrast, Cu, Zn, and Pb presented medium to high enrichment factors and showed a higher proportion of soluble forms, thereby indicating their polluting character.  相似文献   
14.
以共沉淀法制备的纳米Fe3O4为核,以正硅酸乙酯为硅源,通过溶胶-凝胶法制备了SiO2@Fe3O4壳-核结构纳米颗粒,再以钛酸四丁酯为钛源,通过溶胶-凝胶法、经焙烧制得TiO2/SiO2@γ-Fe2O3磁性纳米光催化剂。采用X射线衍射仪、透射电子显微镜、比表面分析仪、振动磁强计对光催化剂的结构进行了表征,以苯酚溶液为模拟废水对光催化剂的光催化性能进行了评价。实验结果表明:经500℃焙烧的光催化剂活性相为锐钛矿型TiO2;在苯酚溶液初始浓度为0.2mmol/L、苯酚溶液pH为7的条件下,COD去除率为70.9%。  相似文献   
15.
工业废水中多金属离子的吸附净化   总被引:2,自引:1,他引:2  
以含有Si、Al、Ca、C元素的矿物材料作为基质,经特定条件处理后造粒成型加工成轻质多孔Si-Al-Ca-C结构的吸附材料。研究了该吸附材料对工业废水中多种金属离子的吸附性能,探讨了影响吸附性能的因素。研究结果表明,在一定条件下,Si-Al-Ca-C吸附材料对工业废水中Al3+、Ca2+、Mn2+、Cu2+、Fe3+、Mg2+、As3+和Zn2+的净化率分别高达99.34%、99.82%、98.26%、98.16%、97.76%、97.01%、100%和89.09%。金属离子残留浓度分别为0.152、0.07、0.012、0.02、0.119、0.311、0和0.259 mg/L,均低于国家污水综合排放标准(GB8978-1996)一级标准。  相似文献   
16.
京津冀地区主要排放源减排对PM2.5污染改善贡献评估   总被引:1,自引:2,他引:1  
研究选取2012年1月和7月作为冬夏两季代表时段,利用CMAQ/2D-VBS模型分析了冬夏两季京津冀地区主要排放源减排30%对改善区域PM_(2.5)污染的效果.结果表明,工业源对PM_(2.5)污染的贡献最大,其次是民用源,但工业源单位减排量贡献低于民用源,交通源和电厂源的整体贡献和单位减排量贡献均较小.工业部门内贡献最大的为钢铁冶金行业,其次是水泥、工业锅炉、炼焦、石灰砖瓦和化工行业.与各部门各物种排放量的比较反映出各排放源贡献大小与其一次PM_(2.5)排放水平高度相关.因京津冀地区冬季NO_x减排对PM_(2.5)形成的促进作用,以及冬季较弱的大气垂直扩散作用,各排放源夏季减排比冬季普遍更有效,交通源、电厂源以及工业源中的水泥、工业锅炉和石灰砖瓦行业夏季减排效果相比冬季优势明显.民用源由于采暖季排放较高而冬季贡献更明显,农业源因秸秆开放燃烧量大,冬季单位减排量贡献十分显著.从同等幅度减排考虑,应将工业源作为控制重点,优先控制其一次PM_(2.5)排放,在部门内进一步重点控制钢铁冶金行业的NO_x和SO_2排放、水泥行业的夏季NO_x排放以及炼焦行业的SO_2和NMVOC排放.民用源排放应着重在冬季采暖期控制.  相似文献   
17.
小流域土地利用结构对氮素输出的影响   总被引:10,自引:9,他引:10  
以丹江口库区的胡家山小流域为研究区,以资源二号卫星影像图为底图,通过实地调查获取胡家山小流域土地利用图,利用ArcGIS的水文模拟、空间分析模块提取15个集水区,并分析其土地利用结构.根据2008年1~12月各个集水区的出口的总氮、硝态氮浓度的监测数据,定量地分析土地利用结构对氮素输出时空变化的影响.结果表明,胡家山小流域内旱地、居民地对氮素输出起显著源作用,与TN、NO-3-N的Pearson相关系数分别为0.869、0.856和0.826、0.867.林地、疏林地、草地等对氮素输出起汇作用,其中林地、草地汇作用显著,与TN、NO-3-N的Pearson相关系数分别为-0.820、-0.851和-0.602、-0.518.土地利用结构是氮素输出空间变化的关键因素,土地利用类型的空间分布使得汇土地利用类型旱地、居民地对小流域氮素输出影响最大;在不同时间尺度上,土地利用结构对氮素输出浓度影响有所不同.年度上,对氮素输出影响最大的是旱地,季节上,春、夏、秋、冬四季对氮素输出影响最大的分别是旱地、居民地、居民地、旱地;土地利用结构对氮素输出浓度的影响受到降雨、气温、人为等因素的作用.  相似文献   
18.

In tropical areas, pioneer occupation fronts steer the rapid expansion of deforestation, contributing to carbon emissions. Up-to-date carbon emission estimates covering the long-term development of such frontiers depend on the availability of high spatial–temporal resolution data. In this paper, we provide a detailed assessment of carbon losses from deforestation and potential forest degradation from fragmentation for one expanding frontier in the Brazilian Amazon. We focused on one of the Amazonia’s hot-spots of forest loss, the BR-163 highway that connects the high productivity agricultural landscapes in Mato Grosso with the exporting harbors of the Amazon. We used multi-decadal (1984–2012) Landsat-based time series on forested and non-forested area in combination with a carbon book-keeping model. We show a 36% reduction in 1984s biomass carbon stocks, which led to the emission of 611.5 TgCO2 between 1985 and 1998 (43.6 TgCO2 year−1) and 959.8 TgCO2 over 1999–2012 (68.5 TgCO2 year−1). Overall, fragmentation-related carbon losses represented 1.88% of total emissions by 2012, with an increasing relevance since 2004. We compared the Brazilian Space Agency deforestation assessment (PRODES) with our data and found that small deforestation polygons not captured by PRODES had increasing importance on estimated deforestation carbon losses since 2000. The comparative analysis improved the understanding of data-source-related uncertainties on carbon estimates and indicated disagreement areas between datasets that could be subject of future research. Furthermore, spatially explicit, annual deforestation and emission estimates like the ones derived from this study are important for setting regional baselines for REDD+ or similar payment for ecosystem services frameworks.

  相似文献   
19.
Regional Environmental Change - By 2014 approximately 2.2 million km2 (~43%) of Brazil’s Legal Amazonia region had been incorporated into an extensive network of 718 protected areas, which...  相似文献   
20.
Regional Environmental Change - The adaptation of social-ecological systems such as managed forests depends largely on decisions taken by forest managers who must choose among a wide range of...  相似文献   
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