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231.
污染物负荷对曝气生物滤池处理效果的影响研究 总被引:1,自引:0,他引:1
考察了进水有机负荷和氨氮负荷对曝气生物滤池出水水质的影响.结果表明,系统COD、氨氮和TN的去除率随进水有机负荷的增加而下降,在氨氮为28.3~33.6 mg/L、TN为39.0~45.8 mg/L条件下,有机负荷小于3.53 kg/(ms3·d)时,出水COD、氨氮和TN分别小于50、5、15 mg/L,去除率分别在85%、85%和65%以上;氨氮和TN的去除率随氨氮负荷的增加而下降,在COD为287.6~313.4 mg/L、氨氮负荷小于0.56 kg/(m3·d)时,出水氨氮小于8 mg/L,去除率在85%以上,出水TN小于15mg/L,去除率在65%以上. 相似文献
232.
提出了一种利用移动监测技术研究区域大气环境中PM2.5/PM10空间分布的方法,并在2004年12月进行了宁波市全市域PM2.5/PM10空间分布的研究。数据显示:相同路径所代表的地区PM2.5和PM10具有很好的相关性,多数路径上PM2.5与PM10数据的相关系数平方在0.95以上,而不同路径上PM2.5与PM10的比值不同。文中给出了宁波市PM2.5/PM10污染的空间分布图,直观地显示出PM2.5/PM10污染的空间分布情况,突出了污染的重点点位和地区。 相似文献
233.
Yu Ren Aijun Ding Tao Wang Xinhua Shen Jia Guo Jiamin Zhang Yan Wang Pengju Xu Xinfeng Wang Jian Gao Jeffrey L. Collett 《Atmospheric environment (Oxford, England : 1994)》2009,43(9):1702-1711
Measurement of ambient gas-phase total peroxides was performed at the summit of Mount Tai (Mt. Tai, 1534 m above sea level) in central-eastern China during March 22–April 24 and June 16–July 20, 2007. The hourly averaged concentration of peroxides was 0.17 ppbv (± 0.16 ppbv, maximum: 1.28 ppbv) and 0.55 ppbv (± 0.67 ppbv, maximum: 3.55 ppbv) in the spring and summer campaigns, respectively. The average concentration of peroxides at Mt. Tai, which is in a heavily polluted region, was much lower than hydrogen peroxide measurements made at some rural mountain sites, suggesting that significant removal processes took place in this region. An examination of diurnal variation and a correlation analysis suggest that these removal processes could include chemical suppression of peroxide production due to the scavenging of peroxy and hydroxy radicals by high NOx, wet removal by clouds/fogs rich in dissolved sulfur dioxide which reacts quickly with peroxides, and photolysis. These sinks competed with photochemical sources of peroxides, resulting in different mean concentrations and diurnal pattern of peroxides in the spring and summer. A principal component analysis was conducted to quantify the major processes that influenced the variation of peroxide concentrations. This analysis shows that in the spring photochemical production was an important source of peroxides, and the major sink was scavenging during upslope transport of polluted and humid air from the lower part of the planetary boundary layer (PBL) and wet removal by synoptic scale clouds. During the summer, highly polluted PBL air (with high NOx) was often associated with very low peroxides due to the chemical suppression of HO2 by high NOx and wet-removal by clouds/fogs in this sulfur-rich atmosphere, especially during the daytime. Higher concentrations of peroxides, which often appeared at mid-nighttime, were mainly associated with subsidence of air masses containing relatively lower concentrations of NOy. 相似文献
234.
Songjun Guo Sheng Wen Xinming Wang Guoying Sheng Jiamo Fu Ping Hu Yingxin Yu 《Atmospheric environment (Oxford, England : 1994)》2009,43(22-23):3489-3495
Formaldehyde and acetaldehyde are two most abundant carbonyls in ambient air. Biogenic emission has been proposed as a significant source other than anthropogenic emissions and atmospheric secondary formation. Here at a forest site in South China, the carbon isotopic compositions of formaldehyde and acetaldehyde emitted from leaves of three tree species (Litsea rotundifolia, Canarium album and Castanea henryi) were measured in comparison with the bulk carbon isotopic compositions of tree leaves. δ13C data of the emitted aldehydes (from ?31‰ to ?46‰) were quite different for tree species, which were all more depleted in 13C than the tree-leaf bulk δ13C values (from ?27‰ to ?32‰). Formaldehyde in ambient air at the forest site had δ13C values different from those of leaf-emitted formaldehyde, indicating other sources for ambient formaldehyde apart from direct emission from leaves, most probably the photooxidation of biogenic hydrocarbon like isoprene and monoterpene. The δ13C differences of acetaldehyde between ambient data and those of tree leaves emission were less than 1‰, implying direct biogenic emission as the dominant source. 相似文献
235.
236.
237.
Gas/particle partitioning of atmospheric PCDD/Fs in a satellite town in Eastern China 总被引:3,自引:0,他引:3
Meng-xia Xu Jian-hua Yan Sheng-yong Lu Xiao-dong Li Tong Chen Ming-jiang Ni Hui-fen Dai Fei Wang Ke-fa Cen 《Chemosphere》2009,76(11):1540-1549
Gas/particle partitioning of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in ambient air was investigated in a satellite town in Eastern China from April 2007 to January 2008 comprehending large temperature variations (from 3 to 34 °C, daily average). Molecular weight, molecular structure and ambient temperatures are the three major factors that govern the gas/particle partitioning of atmospheric PCDD/Fs throughout the year. Generally, good agreements were obtained (except for winter) between measured particulate fractions and theoretical estimates of both the Junge–Pankow adsorption model and Harner Bidleman absorption model using different sets of subcooled liquid vapor pressure and octanol–air partition coefficient (Koa), respectively. Models utilizing estimates, derived from gas chromatographic retention indices (GC-RIs), are more accurate than that of entropy-based. Moreover, during winter, the Koa-based model using the GC-RIs approach performs better on lower chlorinated PCDD/Fs than that of -based. Furthermore, possible sources of mismatch between measured and predicted values in winter (3–7 °C) were discussed. Gas adsorption artifact was demonstrated to be of minor importance for the phenomena observed. On the other hand, large deviations of slopes (mr) and intercepts (br) in logKp vs. plots from theoretical values are observed in the literature data and these are found to be linearly correlated with ambient temperatures (P<0.001) in this study. This indicates that the non-equilibrium partitioning of PCDD/Fs in winter may be significantly influenced by the colder temperatures that may have slowed down the exchange between gaseous and particulate fractions. 相似文献
238.
采用浸渍法制备了CuCoOx/TiO2催化剂,考察了焙烧温度、反应温度、氧含量、NO浓度和空间速度对催化剂催化氧化NO性能的影响,并考察了催化剂的抗硫抗水性能。XRD、TPR和BET分析表明,350℃焙烧的催化剂具有CuCo2O4尖晶石结构,比表面积大,对NO的氧化效果好。在空速为5 000 h-1,NO进口浓度500 mg/m3,含氧量10%的条件下,反应温度300℃时NO转化率可达79.5%,250℃时NO转化率接近50%。该催化剂具有良好的单独抗SO2、抗H2O毒化性能,H2O和SO2同时存在时很快失活。该催化剂可用于不同时含H2O和SO2的含NO气体催化氧化后再吸收处理。 相似文献
239.
沸石改性及其去除水中氨氮的实验研究 总被引:13,自引:4,他引:9
通过实验研究了沸石改性条件及其对水中氨氮吸附去除的影响。结果表明,加热改性与无机酸改性不能显著提高沸石对氨氮的吸附量。利用NaOH改性的最佳浓度为1 mol/L,此条件下对氨氮吸附量可提高到650.68 mg/kg,为天然沸石的2.82倍。利用无机盐改性时,对氨氮吸附效果最好的是NaCl改性沸石,其次为KCl改性沸石与CaCl2改性沸石。随着NaCl溶液浓度和改性时间的增加,改性沸石对氨氮的吸附量显著增加,可达天然沸石的3~4倍;在NaCl浓度为150 g/L与改性时间为18 h条件下,改性沸石对氨氮吸附量可达887.35 mg/kg,为天然沸石的3.84倍。 相似文献
240.
伞罩型湿式脱硫除尘塔入口结构优化模拟 总被引:1,自引:1,他引:0
利用商用CFD软件Fluent,采用k-ε湍流模型和SIMPLE算法,对新型伞罩型湿式脱硫除尘塔内的三维两相流场进行数值模拟,发现了塔内烟气入口处流场所存在的不均匀性。为将其流场调节均匀从而提高脱硫除尘效率,在数值模拟的基础上提出在入口处加装直导流板、阶梯导流板和弯曲导流板,并分析塔内y=0截面速度的分布,以及z=0.21 m截面上的颗粒浓度、速度和压力等参数的分布。结果表明:通过加装阶梯导流板和弯曲导流板均可以将流场调节均匀,达到较理想状态,从而实现高效净化气体的目的。模拟结果对设备的优化设计和实际运行有一定的指导作用。 相似文献