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皮革废水中含大量难降解有机物,导致常规好氧生化处理速率低、效果差。实验考察了在US(超声波)、UV(紫外光)、US/Fenton、UV/Fenton等高级氧化技术强化作用下的生化处理效果,结果表明,在相同水质和实验条件下。废水经US、UV处理30min后可使后续生化反应速率显著提高,分别反应8h、24h后的COD去除率即可达到直接经微生物处理48h后达到的48%,但延长反应时间至48h对COD去除率没有明显提高;Fenton试剂强化US、UV的处理效果要高于单独US、UV工艺.经30min预处理,随后在徽生物作用下分别反应4h和8h即可达到45%和51%的COD去除率,同时延长反应时间也能使最终COD去除率明显提高,反应48h后,COD去除率可分别提高至64%和72%。 相似文献
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Occurrence and photochemical degradation of 17alpha-ethinylestradiol in Acushnet River Estuary 总被引:1,自引:0,他引:1
17alpha-Ethinylestradiol (EE2), a major constituent of common contraceptive pills, and three other estrogenic hormones, estrone (E1), 17beta-estradiol (E2) and mestranol (MeEE2) have been determined in Acushnet River Estuary seawater using a GC-MS technique. Among three estrogenic compounds detected, EE2 has the highest concentration, up to 4.7 ng/l, at which EE2 may affect lobster and other fish abundance in the coastal seawater due to its high biological activity on fish feminization. Two natural estrogenic hormones, E1 and E2 have also been found in the estuary at concentrations up to 1.2 ng/l and 0.83 ng/l, respectively. Although EE2 is persistent to microbial degradation, it can undergo a rapid photodegradation in estuarine seawater under natural sunlight irradiation, with a half-life of less than 1.5 days in spring sunny days. 相似文献
325.
从褐菖鲉肝脏中克隆了热休克蛋白HSC70基因,利用环介导等温扩增技术(loop-mediated isothermal amplification,LAMP)建立HSC70基因的定量检测方法。为检测该方法的可行性,将褐菖鲉分别暴露于石油水溶性成分(water-soluble fraction,WSF) 20、60、180 μg·L-1 1 d后,利用real-time PCR及LAMP技术同时测定褐菖鲉肝HSC70 mRNA表达量,两种方法测定结果基本一致,证实LAMP技术可用于褐菖鲉肝HSC70基因的定量。为更细致了解石油WSF影响褐菖鲉肝脏HSC70基因表达的剂量-效应关系,将褐菖鲉分别暴露于25、50、75、100、125、150、175 μg·L-1 WSF中,5天后采样,用LAMP技术定量检测HSC70 mRNA。结果表明,HSC70 mRNA表达量在50 μg·L-1浓度组即被显著诱导,在75 μg·L-1浓度下达到最大值,这说明褐菖鲉肝HSC70基因对石油污染较敏感,有潜力作为海洋石油污染的生物标志物。 相似文献
326.
ABSTRACTSustainable forest management on a regional scale requires accurate biomass estimation. At present, technologically comprehensive forecasting estimates are generated using process-based ecological models. However, isolation of the ecological factors that cause uncertainty in model behavior is difficult. To solve this problem, this study aimed to construct a meliorization model evaluation framework to explain uncertainty in model behavior with respect to both the mechanisms and algorithms involved in ecological forecasting based on the principle of landsenses ecology. We introduce a complicated ecological driving mechanism to the process-based ecological model using analytical software and algorithms. Subsequently, as a case study, we apply the meliorization model evaluation framework to detect Eucalyptus biomass forest patches at a regional scale (196,158 ha) using the 3PG2 (Physiological Principles in Predicting Growth) model. Our results show that this technique improves the accuracy of ecological simulation for ecological forecasting and prevents new uncertainties from being produced by adding a new driving mechanism to the original model structure. This result was supported by our Eucalyptus biomass simulation using the 3PG2 model, in which ecological factors caused 21.83% and 9.05% uncertainty in model behavior temporal and spatial forecasting, respectively. In conclusion, the systematic meliorization model evaluation framework reported here provides a new method that could be applied to research requiring comprehensive ecological forecasting. Sustainable forest management on regional scales contributes to accurate forest biomass simulation through the principle of landsenses ecology, in which mix-marching data and a meliorization model are combined. 相似文献
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以粉煤灰和钢渣为主要原料,采用水玻璃和Na OH作为碱激发剂,制备出一种具有较高早期强度的地质聚合物胶凝材料。通过实验探讨了各因素对该地质聚合物强度发展的影响。同时,考察了钢渣的加入量对地质聚合物强度的影响。结果表明,当钢渣的加入量(质量分数)为25%,碱加入量为16%,水灰比为0.16,水玻璃加入量为24%时,各组试样的7 d和28 d抗压强度均在20 MPa以上。由XRD、FT-IR进一步分析得出,粉煤灰和钢渣的协同作用制备地质聚合物复合胶凝材料具有较好的早期和后期强度。 相似文献
330.
Zuo Tong How Ina Kristian Francesco Busetti Kathryn L. Linge Cynthia A. Joll 《环境科学学报(英文版)》2017,29(8):2-18
This paper is a critical review of current knowledge of organic chloramines in water systems,including their formation, stability, toxicity, analyticalmethods for detection, and their impact
on drinking water treatment and quality. The term organic chloramines may refer to any
halogenated organic compounds measured as part of combined chlorine (the difference
between themeasured free and total chlorine concentrations), andmay include N-chloramines,
N-chloramino acids, N-chloraldimines and N-chloramides. Organic chloramines can form
when dissolved organic nitrogen or dissolved organic carbon react with either free chlorine
or inorganic chloramines. They are potentially harmful to humans and may exist as an
intermediate for other disinfection by-products. However, little information is available on the
formation or occurrence of organic chloramines in water due to a number of challenges. One of
the biggest challenges for the identification and quantification of organic chloramines in water
systems is the lack of appropriate analytical methods. In addition, many of the organic
chloramines that formduring disinfection are unstable,which results in difficulties in sampling
and detection. To date research has focussed on the study of organic monochloramines.
However, given that breakpoint chlorination is commonly undertaken in water treatment
systems, the formation of organic dichloramines should also be considered. Organic
chloramines can be formed frommany different precursors and pathways. Therefore, studying
the occurrence of their precursors in water systems would enable better prediction and
management of their formation. 相似文献