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61.
安全生产监管是政府的重要职责,直接关系到国家财产和人民生命安全.安全生产监管中,以危险化学品的监管为重中之重.提高安全生产监管的信息化程度是降低监管强度、提高监管效率行之有效的方法.构建了由管理Agent、采集Agent、故障诊断Agent、通信Agent组成的分布式信息采集多Agent系统,将安监局监管中心对危险化学品生产过程监管的信息采集任务下移到企业端,利用多Agent系统实现危险源生产状态参数的采集、监控及分析;设计了该信息采集系统各类Agent的结构和功能.利用多Agent系统实现分散于各企业的危险源生产状态参数的信息采集、监控及分析,预测和诊断生产过程中的异常状况.通过Agent之间的合作、并行求解使危险化学品安全生产信息采集的问题得到较好地解决. 相似文献
62.
以我国210起典型危险化学品火灾爆炸事故为样本,对造成事故的不安全动作进行归类统计,应用云模型云发生器算法计算大类不安全动作的云模型参数值并绘制隶属云图,得出了危险化学品火灾爆炸事故中不安全动作类型和发出者分布规律及特点。结果表明:造成火源型火灾爆炸事故的违规型不安全动作平均发生次数最多,分布不均匀且不稳定,其中现场工作缺乏指导或监护发生次数最多,发出对象为监理;蓄热型火灾爆炸事故中技术型不安全动作分布表现出较大的随机性,其中物料添加不当和隐患排查不彻底发生次数最多,发出对象分别为基层人员和监理。 相似文献
63.
64.
水体颗粒物以及土壤对有机物吸附常数的测定 总被引:10,自引:2,他引:10
本文介绍了用批量平衡测定水体悬浮颗粒物以及土壤对有机物吸附常数的测定方法,并给出实例和方法的注意事项。 相似文献
65.
应用化学清洗剂去除包气带石油污染物的实验研究 总被引:7,自引:0,他引:7
本文探讨了应用化学法清除包气带残油的技术,研究分两个方面,(1)分析包气带土壤与第四纪沉积物对石油烃类的吸附特征,(二)在对单种表面活性剂优选的基础上,确定了清洗效率较高的阴离子-非离子表面活性剂的混合配方,通过一次性淋洗和土柱淋洗实验,了解表面活性剂等清洗剂对油类物质的去除效率。 相似文献
66.
依据经济合作与发展组织(OECD)关于定量结构-活性关系(QSAR)模型构建和使用导则,将780个有机化合物,以4:1的比例随机划分为训练集(624个化合物)和验证集(156个化合物),通过多元线性回归(MLR)方法构建了一个包含12个描述符的有机化合物鱼类生物富集因子(BCF)的QSAR模型。QSAR模型的调整决定系数R2ad j=0.809,去一法交叉验证系数Q2LOO=0.803,外部验证系数Q2EXT=0.732,表明模型具有较好的拟合优度、稳健性和预测能力。采用欧几里德距离方法表征模型应用域,通过威廉姆斯图分析模型离群点,并对模型进行机理解释。所构建的模型,可以用于预测应用域内有机化学品的生物富集因子。 相似文献
67.
本文对化学品登记时所要求的部分健康效应数据一急性毒性和急性刺激做了解释.涉及到的测试参数包括:急性经口毒性、急性经皮毒性、急性吸入毒性、急性皮肤刺激/腐蚀和急性眼睛刺激/腐蚀. 相似文献
68.
Petroleum products are complex mixtures of hydrocarbons. They are important as constituents of fuels and lubricants, and as key raw materials for the chemicals industry. Since there is a potential for accidental releases to the aquatic environment, bioaccumulation of higher hydrocarbons is of concern. Here, the bioconcentration behaviour of two representative hydrocarbons, the dodecane isomers n-dodecane and 2,2,4,6,6-pentamethylheptane (PMH), was investigated in fathead minnows at concentrations in water below their maximum aqueous solubility. The concentration of n-dodecane in fish did not exceed our method limit of detection of 60 μg/kg. In contrast, PMH could be quantified in fish. No significant increase in the ratio of PMH concentrations in fish to water could be detected indicating that an exposure time of 4–10 days is sufficient to approach steady-state. For n-dodecane the upper limit of the bioconcentration factor (BCF) is estimated by dividing the method limit of detection by the exposure concentration and a value of 240 l/kg is derived. For PMH the bioconcentration factor, estimated as the average fish/water concentration ratio during the steady-state part of the experiment, ranges between 880 and 3500 l/kg. The BCFs of both compounds are small compared to their hydrophobicity. Given that both linear and branched hydrocarbons are known to be biotransformed by fish, it appears that efficient metabolism of the test compounds in fathead minnows prevents bioaccumulation. 相似文献
69.
Hollert H Dürr M Holtey-Weber R Islinger M Brack W Färber H Erdinger L Braunbeck T 《Environmental science and pollution research international》2005,12(6):347-360
Goal, Scope and Background In order to evaluate the estrogenic activity of sediments and XAD water extracts of selected sites of the catchment area
of the River Neckar, a river system in Southern Germany, an integrative assessment approach was used to assess the ecological
hazard potential of endocrine-disrupting compounds in sediment and water.
Methods The approach is based on estrogen receptor-mediated vitellogenin synthesis induced in isolated hepatocytes of rainbow trout
and quantified in a non-radioactive dot blot/RNAse protection-assay in parallel to comprehensive chemical analyses of estrogenic
substances.
Results and Discussion Numerous investigated extracts revealed an estrogen activity comparable to that of the positive control (1 nM 17?-estradiol
corresponding to 270 ng/L in the test medium). Based on a concentration factor of 30 in the extracts and a recovery of XAD
resins of approximately 80 %, 17?-estradiol equivalent concentrations between 20 and 26.7 ng/L could be calculated downstream
of a sewage treatment plant (< 0.1 ng/L for a reference site). A comparison of the bioassay-derived Bio-TEQs (toxicity equivalents)
and the Chem-TEQs revealed a high correlation with a Pearson coefficient of 0.85, indicating that the same ranking of the
samples could be obtained with respect to the endocrine disrupting potential with both chemical and bioanalytical analysis.
However, the TEQ concentrations computed from chemical analyses were significantly lower than the bioassay-derived TEQ concentrations.
In fact, in none of the samples, more than 14 % of the vitellogenin-inducing potency could be attributed to the substances
(steroids, alkylphenols, bisphenol A, diethylstilbestrol) analyzed.
A comparison of the endocrine disrupting potential of sediments extracted by the solvents acetone and methanol revealed lower
biological effects for acetone-extracted samples. Possible reasons may be a masking of endocrine effects in acetone extracts
by cytotoxicity, a low extraction efficiency of the solvent acetone, or anti-estrogen potencies of some extracted sediment
compounds.
Using a mass balance approach, the contribution of the compounds analyzed chemically (Chem-TEQs) to the total endocrine activity
(Bio-TEQs) was calculated. Based on the very low detection limits, particularly of the steroids with their high TEF factors,
results revealed that a calculation of the Chem-TEQs is associated with considerable scale inaccuracy: Whereas only 7-15 %
of the biological effectiveness (Bio-TEQs) could be explained by endocrine substances identified above the detection limits,
the assumption of concentrations slightly below the given detection limits would result in a significant over estimation (137-197
%) of the Bio-TEQs. Even the interassay variation of the dot blot assay with different fish donors for primary hepatocyte
(factor 2 - 2.5) is relatively low, when compared to the large range of the Chem-TEQ concentrations (factor 20) obtained when
applying different modes of calculation.
Conclusions and Outlook Overall, only a minor portion of the endocrine activity detected by bioassays could be linked to compounds identified by
chemical analysis. In vitro assays for assessment of endocrine activities are useful as sensitive integrating methods that
provide quantitative estimates of the total activity of particular receptor-mediated responses. Although discrepancies may
also result from different bioanalytical approaches, it is overall likely that bioanalytical and not chemical analytical approaches
give the correct estimate of endocrine disrupting potencies in environmental samples. As a conclusion, assessment of endocrine
disruption based on chemical analysis alone does not appear sufficient and further research into the spectrum of substances
with potential endocrine activity as well as into additive or even synergistic effects in complex environmental samples is
urgently needed. 相似文献
70.