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91.
饮用水中五种有机磷农药的快速检测法 总被引:6,自引:0,他引:6
本文介绍了使用Waters OASIS-HLB固相萃取小柱从水中分离富集敌百虫、敌敌畏、乐果、甲基对硫磷,对硫磷五种有机磷农药的快速检测法。 相似文献
92.
研究了用空气/乙炔火焰原子吸收分光光度法测定水中锶时酸的影响,以及铝和钙的干扰及消除,线性范围0.05~5.00mg/l,最低检测浓度为0.04mg/l,回收率为98.2%~101.4%。 相似文献
93.
测定了九种具不同结构特征的有机磷农药的消光系数、光量子产率和在环境中的光稳定性。探讨了分子结构与光稳定性的关系。结果表明,农药光稳定性主要取决于分子是否具有共轭结构及共轭程度大小;共轭程度愈大,农药的紫外光吸收能力愈强,光量子产率愈小。根据分子结构将有机磷农药分为六类。并以此法对30种结构较为简单的农药的光稳定性作了预测。 相似文献
94.
有机磷农药在土壤环境中的降解转化 总被引:19,自引:1,他引:19
有机磷农药是世界上应用最广泛的农药种类之一 ,它属于比较容易降解的、对环境污染较小的农药。从有机磷农药的性质出发 ,着重讨论了有机磷农药的水解、光解和微生物降解 ,这也是有机磷农药在土壤中的主要降解转化过程 相似文献
95.
96.
有机磷农药废水碱性水解生物处理技术 总被引:2,自引:0,他引:2
本文报道了碱性水解和生物氧化两步法,处理有机磷农药-乐果、甲胺磷生产废水的研究结果.废水经碱性水解后,COD和有机磷浓度基本不变,但可生化性有明显改善.在遵循常规生物处理必须满足的条件下,碱性废水进一步用间歇或连续活性污泥法处理.COD去除率90%左右,有机磷去除率85%以上,有机磷含量以毒性磷计小于0.5mg/L.深入考察了碱解剂种类、水溶液的pH和温度等各种因素对碱性水解的影响,结果表明:NaOH作碱解剂时的碱解速率比Ca(OH),提高28%;碱解速率随pH和温度的升高而增大,pH每增加一个单位,碱解速率增加2~11倍;温度每升高10℃,碱解速率增加2~5倍. 相似文献
97.
通过计算43种有机磷农药的各种结构参数,运用多元线性回归分析方法比较了适用于有机磷农药色谱保留值的定量关系表达式,建立了有机磷农药结构参数对色谱保留值的QSPR模型.模型分析表明:磷酸酯与硫逐磷酸酯两类有机磷农药的模型非交叉验证相关系数R2分别为0.991和0.998,标准误差SE分别为0.0539和0.2874,交叉验证相关系数Q2分别为0.976和0.990,标准偏差Scv分别为0.086和0.610.在已知磷酸酯与硫逐磷酸酯两类有机磷农药结构参数的情况下,此模型可有助于有机磷农药的色谱分析. 相似文献
98.
Organophosphorus flame retardants and plasticizers in the atmosphere of the North Sea 总被引:1,自引:0,他引:1
Möller A Xie Z Caba A Sturm R Ebinghaus R 《Environmental pollution (Barking, Essex : 1987)》2011,159(12):3660-3665
Air samples collected in the German part of the North Sea from March to July 2010 were investigated for organophosphorus compounds (OPs) being applied as flame retardants and plasticizers. The ∑8OPs concentration ranged from 110 to 1400 pg m−3 while tris(2-chloroisopropyl) phosphate (TCPP) dominated all samples with individual concentrations up to 1200 pg m−3. The highest concentrations were observed in continental air masses showing the high influence of industrialized regions including production sites on atmospheric emissions and concentrations. The occurrence of OPs even in oceanic/Arctic air masses shows that OPs can undergo long-range atmospheric transport. Dry particle-bound deposition fluxes from 9 to 240 ng m−2 d−1 for ∑8OPs were estimated leading to a minimum annual flux of 710 ± 580 kg y−1 OPs into the German North Sea. This study presents the first occurrence of OPs in the marine atmosphere together with important information on their long-range transport potential. 相似文献
99.
Zhang Y Wu JP Luo XJ Wang J Chen SJ Mai BX 《Environmental pollution (Barking, Essex : 1987)》2011,159(12):3647-3652
Information on tissue distribution of Dechlorane Plus (DP) and its dechlorinated analogs in wildlife is scarce. DP isomers and two dechlorinated compounds, anti-Cl11-DP and anti-Cl10-DP, were examined in the muscle, liver, and brain tissues of two bottom fish species collected from an electronic waste recycling site, South China. The median levels of syn-, anti-, and anti-Cl11-DP isomers in the tissues ranged 0.18-39.1, 0.22-52.9, and 0.01-5.63 ng/g wet wt, respectively. Anti-Cl10-DP was only detected in one muscle sample of mud carp (0.01 ng/g wet wt), although it was consistently detected in the sediments (0.42-0.83 ng/g dry wt). Preferential distribution in liver relative to muscle was observed for syn-DP and anti-Cl11-DP. However, a high persistent retention in the brain compared to the liver was observed for anti-DP, suggesting that this isomer can across the blood-brain barrier of fish, and may cause adverse effects to the nervous system in the exposed biota. 相似文献
100.
Dechlorane Plus (DP) has been determined in surface sediments from three Chinese coastal bays, e.g. Jiaozhou, Sishili and Taozi Bay in North China. DP concentrations ranged from <1.2 to 187 pg g−1 dry weight (dw) (mean: 24.7 pg g−1 dw) in Jiaozhou Bay, <1.2 to 135 pg g−1 dw (mean 69.9 pg g−1 dw) in Sishili Bay and <1.2 to 66.7 pg g−1 dw (mean: 40.4 pg g−1 dw) in Taozi Bay, respectively. Additionally, two dechlorinated species were quantified, which accounted for 0.6-5.1% of the ∑DP concentration.The fsyn values (syn-isomer/(syn- + anti-isomer)) in sediments from Jiaozhou Bay (mean 0.29) were close to the technical DP mixture (0.2-0.4), probably indicating local inputs of DP. In contrast, sediments in Sishili and Taozi Bay showed much lower fsyn values (mean 0.16). During transportation the DP isomers are subject to stereo selective degradation which partly resulted in the relative enrichment of anti-DP in coastal sediments. 相似文献