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291.
292.
人工浮床对汾江河水质净化的研究 总被引:1,自引:0,他引:1
对佛山市汾江河内布置浮床的水域的7个断面进行采样监测,分析了布置浮床侧与未布置浮床侧各水质指标的差异,以考察人工浮床对汾江河水质的净化效果。同时比较了圆币草、水罂粟、梭鱼草、狐尾草、美人蕉和鸢尾6种浮床植物的生物量和氮磷吸收量。结果表明,布置人工浮床一侧的水质TN、TP、COD和NH4+-N含量均显著低于未布置浮床一侧的水质,表明人工浮床对水体水质的有净化效果。总面积约4 900 m2的浮床植物经过3个月的生长,从水体中共吸收了192.5 kg的氮和76.1 kg的磷。6种浮床植物中,狐尾草的净增生物量最高,达到64.2 kg/m2;圆币草次之,为62.2 kg/m2。狐尾草和圆币草对氮磷的吸收能力在6种植物中处于较高水平,每平方米狐尾草和圆币草从水体中分别吸收了51.61g氮、19.79 g磷和46.90 g氮、22.93 g磷。综合比较得出,狐尾草和圆币草在生物量和氮磷吸收量上均保持在较高水平,是较好的浮床植物。本研究为人工浮床在南方类似河流中的应用及植物选择提供了参考依据。 相似文献
293.
根据污染源头控制和废水回用的要求,对典型棉针织染整厂的不同生产过程废水排水水质特征进行了统计分析,提出了较实用的废水源头清浊分流方案。在此基础上重点研究了混凝-臭氧组合工艺对清废水处理效果,确定了最优的工艺条件。结果表明,清废水主要为洗水,占废水总量的25%~30%;混凝-臭氧组合工艺的最优工艺条件为:pH为6~9,PAC投加量为48 mg/L,PAM投加量为1.0 mg/L,臭氧接触时间为12 min(臭氧浓度为14.5 mg/L),这时,清废水COD、色度去除率分别为71%和98%,实践证明,出水水质完全能够满足染整生产。 相似文献
294.
偕胺肟合铁(Ⅲ)纤维对α-萘酚的吸附 总被引:1,自引:0,他引:1
以腈纶纤维为原料络合Fe3+制得偕胺肟合铁(Ⅲ)纤维,用其处理α-萘酚溶液,研究了偕胺肟合铁(Ⅲ)纤维对α-萘酚的吸附工艺条件和吸附动力学参数。实验结果表明,偕胺肟合铁(Ⅲ)纤维对α-萘酚的最佳吸附工艺条件为pH=3.0、吸附温度313.15K和吸附时间45min。在最佳工艺条件下,偕胺肟合铁(Ⅲ)纤维对α-萘酚的吸附在所研究的α-萘酚浓度范围内符合Freundlich等温吸附方程。未达到饱和吸附前,偕胺肟合铁(Ⅲ)纤维对α-萘酚的吸附符合一级反应动力学特征。 相似文献
295.
296.
高膜通量厌氧微网生物反应器处理生活污水的研究 总被引:3,自引:1,他引:2
将动态膜技术与厌氧膜生物反应器相结合,形成一体式厌氧微网生物反应器(AnFBR),用于城市生活污水的处理,研究了在高膜通量条件下,AnFBR的运行情况和对生活污水的处理效果。结果表明,AnFBR在膜通量为72 L/(m2.h)条件下可连续稳定运行40 d;系统对COD平均去除率为58.4%,对TN和NH3-N有一定的去除效果;出水SS最高为15.0 mg/L,出水中污染物粒径在10μm以下;微网动态膜对小分子物质的截留量不高,但对分子量大于1 000 kU的物质有明显的截留效果,进水中的大部分大分子物质被转化为小分子物质;AnFBR在保留了泥水分离特点的情况下还具有结构简单、膜通量高、微网过滤周期长等优点。 相似文献
297.
Xueyuan Wang Xin-Zhong Liang Weimei Jiang Zhining Tao Julian X.L. Wang Hongnian Liu Zhiwei Han Shuyan Liu Yuyan Zhang Georg A. Grell Steven E. Peckham 《Atmospheric environment (Oxford, England : 1994)》2010,44(5):660-669
This study develops fine temporal (seasonal, day-of-week, diurnal) and vertical allocations of anthropogenic emissions for the TRACE-P inventory and evaluates their impacts on the East Asian air quality prediction using WRF-Chem simulations in July 2001 at 30-km grid spacing against available surface measurements from EANET and NEMCC. For NO2 and SO2, the diurnal and vertical redistributions of emissions play essential roles, while the day-of-week variation is less important. When all incorporated, WRF-Chem best simulates observations of surface NO2 and SO2 concentrations, while using the default emissions produces the worst result. The sensitivity is especially large over major cities and industrial areas, where surface NO2 and SO2 concentrations are reduced by respectively 3–7 and 6–12 ppbv when using the scaled emissions. The incorporation of all the three redistributions of emissions simulates surface O3 concentrations higher by 4–8 ppbv at night and 2–4 ppbv in daytime over broad areas of northern, eastern and central China. To this sensitivity, the diurnal redistribution contributes more than the other two. 相似文献
298.
Renbin Zhu Yashu Liu Hua Xu Tao Huang Jianjun Sun Erdeng Ma Liguang Sun 《Atmospheric environment (Oxford, England : 1994)》2010,44(3):304-311
During the summertime of 2007/2008, carbon dioxide (CO2) and methane (CH4) fluxes across air–water interface were investigated in the littoral zones of Lake Mochou and Lake Tuanjie, east Antarctica, using a static chamber technique. The mean fluxes of CO2 and CH4 were ?70.8 mgCO2 m?2 h?1 and 144.6 μgCH4 m?2 h?1, respectively, in the littoral zone of Lake Mochou; The mean fluxes were ?36.9 mgCO2 m?2 h?1 and 109.8 μgCH4 m?2 h?1, respectively, in the littoral zone of Lake Tuanjie. Their fluxes showed large temporal and spatial dynamics. The CO2 fluxes showed a significantly negative correlation with daily total radiation (DTR) and a weakly negative correlation with air temperature and water temperature, indicating that sunlight intensity controlled the magnitude of CO2 fluxes from the open lakes. The CH4 fluxes significantly correlated with local air temperature, water table and total dissolved solids (TDS), indicating that they were the predominant factors influencing CH4 fluxes. Summertime CO2 budgets in the littoral zones of Lake Mochou and Lake Tuanjie were estimated to be ?152.9 gCO2 m?2 and ?79.7 gCO2 m?2, respectively, and net CH4 emissions were estimated to be 312.3 mgCH4 m?2 and 237.2 mgCH4 m?2, respectively. Our results show that shallow, open, alga-rich lakes might be strong summertime CO2 absorbers and small CH4 emitters during the open water in coastal Antarctica. 相似文献
299.
Junyu Zheng Liuju Zhong Tao Wang Peter K.K. Louie Zhicheng Li 《Atmospheric environment (Oxford, England : 1994)》2010,44(6):814-823
The ambient air quality monitoring data of 2006 and 2007 from a recently established Pearl River Delta (PRD) regional air quality monitoring network are analyzed to investigate the characteristics of ground-level ozone in the region. Four sites covering urban, suburban, rural and coastal areas are selected as representatives for detailed analysis in this paper. The results show that there are distinct seasonal and diurnal cycles in ground-level ozone across the PRD region. Low ozone concentrations are generally observed in summer, while high O3 levels are typically found in autumn. The O3 diurnal variations in the urban areas are larger than those at the rural sites. The O3 concentrations showed no statistically significant difference between weekend and weekdays in contrast to the findings in many other urban areas in the world. The average ozone concentrations are lower in urban areas compared to the sites outside urban centers. Back trajectories are used to show the major air-mass transport patterns and to examine the changes in ozone from the respective upwind sites to a site in the center of the PRD (Wanqingsha). The results show higher average ozone concentrations at the upwind sites in the continental and coastal air masses, but higher 1 h-max O3 concentrations (by 8–16 ppbv) at the center PRD site under each of air-mass category, suggesting that the ozone pollution in the PRD region exhibits both regional and super-regional characteristics. 相似文献
300.
Guofeng Shen Wei Wang Yifeng Yang Chen Zhu Yujia Min Miao Xue Junnan Ding Wei Li Bin Wang Huizhong Shen Rong Wang Xilong Wang Shu Tao 《Atmospheric environment (Oxford, England : 1994)》2010,44(39):5237-5243
Coal consumption is one important contributor to energy production, and is regarded as one of the most important sources of air pollutants that have considerable impacts on human health and climate change. Emissions of polycyclic aromatic hydrocarbons (PAHs) from coal combustion were studied in a typical stove. Emission factors (EFs) of 16 EPA priority PAHs from tested coals ranged from 6.25 ± 1.16 mg kg?1 (anthracite) to 253 ± 170 mg kg?1 (bituminous), with NAP and PHE dominated in gaseous and particulate phases, respectively. Size distributions of particulate phase PAHs from tested coals showed that they were mostly associated with particulate matter (PM) with size either between 0.7 and 2.1 μm or less than 0.4 μm (PM0.4). In the latter category, not only were more PAHs present in PM0.4, but also contained higher fractions of high molecular weight PAHs. Generally, there were more than 89% of total particulate phase PAHs associated with PM2.5. Gas-particle partitioning of freshly emitted PAHs from residential coal combustions were thought to be mainly controlled by absorption rather than adsorption, which is similar to those from other sources. Besides, the influence of fuel properties and combustion conditions was further investigated by using stepwise regression analysis, which indicated that almost 57 ± 10% of total variations in PAH EFs can be accounted for by moisture and volatile matter content of coal in residential combustion. 相似文献