全文获取类型
收费全文 | 2995篇 |
免费 | 413篇 |
国内免费 | 1101篇 |
专业分类
安全科学 | 503篇 |
废物处理 | 121篇 |
环保管理 | 203篇 |
综合类 | 2641篇 |
基础理论 | 368篇 |
污染及防治 | 263篇 |
评价与监测 | 268篇 |
社会与环境 | 47篇 |
灾害及防治 | 95篇 |
出版年
2024年 | 53篇 |
2023年 | 119篇 |
2022年 | 166篇 |
2021年 | 224篇 |
2020年 | 193篇 |
2019年 | 186篇 |
2018年 | 148篇 |
2017年 | 132篇 |
2016年 | 140篇 |
2015年 | 195篇 |
2014年 | 309篇 |
2013年 | 200篇 |
2012年 | 222篇 |
2011年 | 210篇 |
2010年 | 152篇 |
2009年 | 165篇 |
2008年 | 189篇 |
2007年 | 190篇 |
2006年 | 182篇 |
2005年 | 174篇 |
2004年 | 145篇 |
2003年 | 87篇 |
2002年 | 111篇 |
2001年 | 84篇 |
2000年 | 83篇 |
1999年 | 78篇 |
1998年 | 60篇 |
1997年 | 52篇 |
1996年 | 61篇 |
1995年 | 40篇 |
1994年 | 38篇 |
1993年 | 25篇 |
1992年 | 32篇 |
1991年 | 27篇 |
1990年 | 9篇 |
1989年 | 17篇 |
1988年 | 4篇 |
1987年 | 6篇 |
1986年 | 1篇 |
排序方式: 共有4509条查询结果,搜索用时 62 毫秒
171.
青岛大气气溶胶中氨基化合物的分布特征 总被引:2,自引:1,他引:1
氨基化合物是大气气溶胶和雨水中常被检出的一类有机氮化合物,由于其可作为生物生长直接的氮源,因此可能对海洋生态系统产生直接作用.利用2008年1~12月在青岛采集的66个总悬浮颗粒物样品,采用邻苯二甲醛/N-乙酰-L-半胱氨酸柱前衍生高效液相色谱法,分析了其中溶解态(DAC)和颗粒态氨基化合物(PAC)的浓度.气溶胶中DAC浓度为2.4~40.9nmol·m-3,在春季最高,夏季次之,秋季、冬季最低.PAC浓度为0.7~76.1nmol·m-3,呈现春季冬季秋季夏季的变化趋势.不同季节氨基化合物的组成不同.依据气团的后向轨迹,气溶胶样品可分为受北方陆源、南方陆源和海洋源影响,DAC和PAC在受南方陆源影响的气溶胶中浓度最高,北方陆源次之,海洋源气溶胶中最低.不同来源的气溶胶中氨基化合物的组成不同,蛋白质类氨基化合物对总氨基化合物的贡献在海洋源气溶胶中最高,在南方源气溶胶中最低. 相似文献
172.
173.
反硝化反应受到抑制导致硝化反应消耗的碱度未能得到平衡,偏低的PH使微生物的代谢速度减慢。因而生化系统的处理能力降低,同时较高的亚硝酸盐氮、硝酸盐氮含量使二沉池极易发生污泥上浮。通过增加有机负荷来降低溶解氧确实可以抑制硝化反应。让问题得到缓解,但通过污泥龄来控制硝化程度,确保比较彻底的反硝化、氮最大程度的得以脱除,使生化系统形成良性循环,这才是根本的解决措施。 相似文献
174.
当前,我国各种污水处理的构筑物在设计上大部分都是基于理想情况,虽然在设计中已经比较保守,考虑到不利因素,但往往仍难以达到预期的处理效果。通过对水处理构筑物的水流流态进行分析,辅以计算流体力学和计算机技术,可以模拟并改进构筑物中的流体流态,进而提高处理效率,为管理提供科学依据。 相似文献
175.
以Al2(SO)4和PDMDAAC为原料进行了无机-有机复合絮凝剂的复合实验研制,确定其制备工艺条件,并对油田现场采集的钻井废水作絮凝沉降实验,所研制的PAS-PDMDAAC复合絮凝剂对COD的去除效率可大大提高. 相似文献
176.
177.
Bioaerosols from wastewater treatment processes are a significant subgroup of atmospheric aerosols. In the present study,airborne microorganisms generated from a wastewater treatment station(WWTS) that uses an oxidation ditch process were diminished by ventilation.Conventional sampling and detection methods combined with cloning/sequencing techniques were applied to determine the groups,concentrations,size distributions,and species diversity of airborne microorganisms before and after ventilation. There were 3021 ± 537 CFU/m3 of airborne bacteria and 926 ± 132 CFU/m3 of airborne fungi present in the WWTS bioaerosol.Results showed that the ventilation reduced airborne microorganisms significantly compared to the air in the WWTS. Over 60% of airborne bacteria and airborne fungi could be reduced after4 hr of air exchange. The highest removal(92.1% for airborne bacteria and 89.1% for fungi) was achieved for 0.65–1.1 μm sized particles. The bioaerosol particles over 4.7 μm were also reduced effectively. Large particles tended to be lost by gravitational settling and small particles were generally carried away,which led to the relatively easy reduction of bioaerosol particles0.65–1.1 μm and over 4.7 μm in size. An obvious variation occurred in the structure of the bacterial communities when ventilation was applied to control the airborne microorganisms in enclosed spaces. 相似文献
178.
Genotoxicity removal of reclaimed water during ozonation 总被引:1,自引:0,他引:1
Genotoxicity in wastewater and reclaimed water now is gaining increased attention because of genotoxins' potential damage to the ecosystem and human health. The effect of ozonation on genotoxicity in reclaimed water was investigated. It was found that ozonation decreased the genotoxicy dramatically in three tertiary treatment plants. In the further batch ozonation experiment in laboratory,secondary effluent sample used exhibited the genotoxicity of(41.1 ± 4.1) μg 4NQO/L. Ozonation with a dose of 10 mg O3/L completely removed the genotoxicity in secondary effluent. However,after ozonation, the dissolved organic carbonvalue of the sample didn't change much but the specific ultraviolet absorbance(SUVA) value dropped sharply. With the help of Fourier transform infrared spectroscopy, ozonation was found to change chemical aliphatic carbon and C–O of the dissolved arganic matter, which might be the reason of the significant decreases of SUVA and genotoxicity. 相似文献
179.
Xiuying Zhao Xinming Wang Xiang Ding Quanfu He Zhou Zhang Tengyu Liu Xiaoxin Fu Bo Gao Yunpeng Wang Yanli Zhang Xuejiao Deng Dui Wu 《环境科学学报(英文版)》2014,26(1):110-121
Organic acids as important constituents of organic aerosols not only influence the aerosols' hygroscopic property, but also enhance the formation of new particles and secondary organic aerosols. This study reported organic acids including C14–C32fatty acids, C4–C9dicarboxylic acids and aromatic acids in PM2.5collected during winter 2009 at six typical urban, suburban and rural sites in the Pearl River Delta region. Averaged concentrations of C14–C32fatty acids, aromatic acids and C4– C9 dicarboxylic acids were 157, 72.5 and 50.7 ng/m3, respectively. They totally accounted for 1.7% of measured organic carbon. C20–C32fatty acids mainly deriving from higher plant wax showed the highest concentration at the upwind rural site with more vegetation around, while C14–C18fatty acids were more abundant at urban and suburban sites, and dicarboxylic acids and aromatic acids except 1,4-phthalic acid peaked at the downwind rural site. Succinic and azelaic acid were the most abundant among C4–C9dicarboxylic acids, and 1,2-phthalic and 1,4-phthalic acid were dominant aromatic acids. Dicarboxylic acids and aromatic acids exhibited significant mutual correlations except for 1,4-phthalic acid, which was probably primarily emitted from combustion of solid wastes containing polyethylene terephthalate plastics. Spatial patterns and correlations with typical source tracers suggested that C14–C32fatty acids were mainly primary while dicarboxylic and aromatic acids were largely secondary. Principal component analysis resolved six sources including biomass burning, natural higher plant wax, two mixed anthropogenic and two secondary sources; further multiple linear regression revealed their contributions to individual organic acids. It turned out that more than 70% of C14–C18fatty acids were attributed to anthropogenic sources, about 50%–85% of the C20–C32fatty acids were attributed to natural sources, 80%–95% of dicarboxylic acids and 1,2-phthalic acid were secondary in contrast with that 81% of 1,4-phthalic acid was primary. 相似文献
180.