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41.
移动床生物膜反应器充氧能力的试验研究 总被引:5,自引:0,他引:5
对移动床生物膜反应器的充氧能力进行了试验研究,结果表明:反应器充氧能力在添加填料比无填料时大;在悬浮载体能够均匀流化的填充率范围内,反应器充氧能力随着填充率的增大而增大;当填充率大于可以均匀流化的最大填充率时,反应器的充氧能力略有下降。 相似文献
42.
Marty D. Matlock Kevin Ray Kasprzak G. Scott Osborn 《Journal of the American Water Resources Association》2003,39(2):267-275
ABSTRACT: The lower reaches of the Arroyo Colorado have historically failed to meet their use under subsection 303(b) of the U.S. Clean Water Act due to fecal coliform bacteria and low dissolved oxygen (DO). Fish kills, especially at the tidal confluence at the Port of Harlingen, Texas, have been reported. Oxygen demand from sediment (SOD) for a river typically has two states‐diffusion limited SOD (SOD) and potential SOD (pSOD), expressed when sediment is resuspended through increased flow or other disturbances. The objective of this research was to measure SOD in the Arroyo Colorado River in situ, estimate pSOD ex situ, and evaluate the relationship between SOD and the depositional environment. We measured SOD and pSOD in the Arroyo Colorado River at up to eight sites over three sampling events. We identified the sample sites based on a modified Rosgen geomorphic index for streambed stabilization. Sites with high sediment deposition potential had high SOD. The average values of SOD between sites were 0.62 g/m2/day (standard deviation 0.38 g/m2/day) and ranged from 0.13 to 1.2 g/m2/day. Potential SOD values ranged from as low as 19.2 to as high as 2,779 g/m3 sediment/ day. Potential SOD can serve as an indicator of the possible impact of SOD from resuspended sediment in stream systems. 相似文献
43.
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45.
人民生活水平的提高使人民对室内环境的舒适程度提出了更高要求 ,室内装饰织物的用量迅速增加 ,室内装饰织物在燃烧时会释放出大量有毒物质和热量 ,对人及环境构成了巨大危害。因此 ,研究装饰织物的燃烧特性非常重要。笔者利用热重 -差热 (TG -DTA)分析仪对纯棉、棉麻和腈纶这几种典型的装饰织物在不同的氧气浓度 (10 % ,15 % ,2 1% )和升温速率 (10K/min ,30K/min)条件下进行了热重分析 (TG)和差热分析 (DTA)实验 ,研究了它们的燃烧特性 ,并着重进行了不同氧浓度下的对比研究 ,发现试样的燃烧分为两个阶段。建立了以一级反应模型为主的动力学方程 ,并得出了各阶段的动力学参数、表观活化能和频率因子。 相似文献
46.
Davey L. Jones John F. Farrar Kevin K. Newsham 《Water, Air, & Soil Pollution: Focus》2004,4(6):169-175
Amino acids constitute one of the largest inputs of organic nitrogen (N) to most polar soils and have been hypothesized to be important in regulating vegetational succession and productivity in Arctic ecosystems. Our understanding of amino acid cycling in these soils, however, is poor. The aim of this study was to investigate the size and rate of turnover of the amino acid pool in a range of Arctic and Antarctic soils. Our results indicate that in polar soils with either high or low ornithogenic inputs the amino acid pool is small in comparison to the inorganic N pool (NO–3 and NH+4). The free amino acid pool constituted only a small proportion of the total dissolved organic nitrogen (DON) pool in these soils. Here we show that these low concentrations may be due to rapid use by the soil microbial community in both Arctic and Antarctic soils. The turnover of the amino acid pool in soil was extremely rapid, with a half-life ranging from 2 to 24 h, indicating that this N pool can be turned over many hundred times each summer when polar soils are frequently unfrozen. The implications of amino acids in N cycling and plant and microbial nutrition are discussed. 相似文献
47.
Impact of Land Use on Soluble Organic Nitrogen in Soil 总被引:5,自引:0,他引:5
Victoria B. Willett James J. Green Andrew J. Macdonald John A. Baddeley Georg Cadisch Steven M. J. Francis Keith W. T. Goulding Gary Saunders Elizabeth A. Stockdale Christine A. Watson David L. Jones 《Water, Air, & Soil Pollution: Focus》2004,4(6):53-60
Although it has been hypothesized that soluble organic nitrogen (SON) plays a central role in regulating productivity in some terrestrial ecosystems, the factors controlling the size of the SON pool in soil remain poorly understood. Therefore our principal aim in this work was to assess the impact of seven different land use systems (rough and managed grassland, deciduous and coniferous woodland, heathland, wetland and tilled land) on the size of the SON and inorganic N (NO
3
–
, NH
4
+
) pools in the surface soil layer (0–15 cm). After extraction with deionised water, we found that in most cases the size of the water extractable organic N (WEON) pool was similar in size to the inorganic N pool. In contrast, the KCl extractable organic N (KClEON) pool constituted the dominant form of soluble N in soils under all land uses, perhaps indicating that significant amounts were held on the soil exchange phase. In contrast to inorganic N, which varied significantly with land use, the size of the KClEON and WEON pool was similar for all land uses with the exception of KClEON in tilled land, where significantly lower amounts were observed. We conclude that SON constitutes an important soil N pool in a broad range of land uses, and that its role in microbial N assimilation, plant nutrition and ecosystem responses to atmospheric N deposition warrants further attention.
SAFRD, University of Newcastle, Newcastle-upon-Tyne, NE1 7RU, U.K. 相似文献
48.
在对废水中的BOD5进行常规分析时,采用化学稀释法操作繁琐,对稀释倍数估计易发生错误。而利用TraK装置测试样品时,无须进行稀释和化学分析。用该装置对标准样品BOD5的测定结果表明:准确度相对误差为-3.3%~4.3%,精密度的相对误差为-3.5%~5.6%。该仪器测试性能可靠,数据准确度、精密度合格。与化学法对照分析表明,相对误差都在容许范围内,即在可接受范围内。 相似文献
49.
利用紫外-可见光谱与三维荧光光谱,结合拉格朗日混合单粒子轨道模型及火点图,研究了重庆2013年夏、冬两季雨水DOM光谱特征,并对其来源进行解析.结果表明,雨水DOM与水体、土壤DOM具有类似性质光谱特征,证明降雨DOM也是陆地及水环境中DOM地化特征的重要贡献者.雨水DOM中DOC含量为0.88~12.80 mg·L-1,CDOM含量在3.17~21.11m-1之间,夏、冬两季降雨DOM差异明显(P0.05).与夏季相比,冬季降雨DOM分子量较小,芳香性程度较低,腐殖化程度也更低,输入主要以本地和短距离输送为主;而夏季DOM来源较分散.尽管吸收和荧光光谱可用于解析雨水DOM组成和来源,但在光谱特征的解析和来源识别上与其他来源DOM有所区别,传统"内、外源区分"并不适用于雨水DOM. 相似文献
50.
针对重霾污染,在西安市冬季重污染日(2015-11-30~2015-12-09)和清洁日(2016-01-13~2016-01-22)各进行了为期10d的PM_(2.5)采集,测量其中的有机碳、元素碳,及NH_4~+、NO_3~-、SO_4~(2-)等无机水溶性离子,探讨两种污染条件下的组分特征及其成因.结果表明:观测期,重霾日和清洁日PM_(2.5)质量浓度分别为(170±47.5)μg·m~(-3)和(48.6±17.9)μg·m~(-3),且重霾日伴随低能见度、高湿静风等多种不利气象条件;重霾日二次无机离子(NH_4~+、NO_3~-、SO_4~(2-))组分占PM_(2.5)质量浓度的49.8%±13.1%,而清洁日为19.4%±5.95%,并且重霾日硫氧化速率(sulfur oxidation ratio,SOR)和氮氧化速率(nitrogen oxidation ratio,NOR)分别为0.282±0.157和0.269±0.124,远高于清洁日(SOR和NOR分别为0.189±0.057和0.077±0.046),重霾日二次有机组分浓度[(6.22±3.87)μg·m~(-3)]是清洁日[(1.44±1.63)μg·m~(-3)]的5倍,表明二次污染及不利气象条件是造成重霾期间相关组分浓度升高的重要原因.最后,通过二氯荧光黄双乙酸盐(2',7'-DCFH)化学荧光分析法测定了其中活性氧物质(reactive oxygen species,ROS)的浓度,探讨其对于二次无机组分形成的影响,结果表明观测期ROS平均浓度(以H_2O_2计)分别为(4.99±1.54)nmol·m~(-3)(重霾期),(0.492±0.356)nmol·m~(-3)(清洁期),二次反应及积累效应可能是西安重霾条件下ROS浓度升高的主要原因.NO_3~-、SO_4~(2-)与ROS均呈现正相关(P0.05),表明ROS可能通过二次氧化过程参与到二次无机组分形成过程中. 相似文献