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Jeong Kyungjun Hong Jiyeon Lee Yongjin Yang Jiyeon Lim Youngwook Shin Dongchun Kim Changsoo 《Environmental science and pollution research international》2021,28(28):37506-37519
Environmental Science and Pollution Research - Preschool children aged 3–6 years are vulnerable to exposed to particulate matter (“PM10” and “PM2.5”). It is required... 相似文献
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Kahouadji Lyes Batchvarov Assen Adebayo Idris T. Jenkins Zachary Shin Seungwon Chergui Jalel Juric Damir Matar Omar K. 《Environmental Fluid Mechanics》2022,22(2):367-382
Environmental Fluid Mechanics - In this article, we present a full three-dimensional numerical study of thin liquid films falling on a vertical surface, by solving the full three-dimensional... 相似文献
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Juntaek LIM Seung Gu SHIN Seungyong LEE Seokhwan HWANG 《Frontiers of Environmental Science & Engineering》2011,5(1):28-39
Real-time quantitative polymerase chain reaction (qPCR) has gained popularity as a technique to detect and quantify a specific group of target microorganisms from various environmental samples including soil, water, sediments, and sludge. Although qPCR is a very useful technique for nucleic acid quantification, accurately quantifying the target microbial group strongly depends on the quality of the primer and probe used. Many aspects of conducting qPCR assays have become increasingly routine and automated; however, one of the most important aspects, designing and selecting primer and probe sets, is often a somewhat arcane process. In many cases, failed or non-specific amplification can be attributed to improperly designed primer-probe sets. This paper is intended to provide guidelines and general principles for designing group-specific primers and probes for qPCR assays. We demonstrate the effectiveness of these guidelines by reviewing the use of qPCR to study anaerobic processes and biologic nutrient removal processes. qPCR assays using group-specific primers and probes designed with this method, have been used to successfully quantify 16S ribosomal Ribonucleic Acid (16S rRNA) gene copy numbers from target methanogenic and ammonia-oxidizing bacteria in various laboratory- and full-scale biologic processes. Researchers with a good command of primer and probe design can use qPCR as a valuable tool to study biodiversity and to develop more efficient control strategies for biologic processes. 相似文献
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Polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and dioxin-like polychlorinated biphenyls (DL-PCBs) were measured in ambient air samples collected from different parts of South Korea in 2008, and the measured levels were used for assessing the spatial and temporal distribution of atmospheric PCDDFs and DL-PCBs in South Korea. The average concentrations of atmospheric PCDD/Fs and DL-PCBs among the 37 sites were 28 fg I-TEQ m−3 (ND ∼ 617) and 1 fg WHO-TEQ m−3 (ND ∼ 0.016). Elevated atmospheric levels of PCDD/Fs and DL-PCBs observed at residential/industrial sites and in the north-west of Korea, indicated a potential contribution and impacts of anthropogenic sources of PCDD/Fs and DL-PCBs. These levels were similar or lower than those previously reported in other ambient air surveys. Average concentrations of PCDD/Fs showed small seasonal variations (ANOVA analysis, p = 0.144). The highest concentrations of PCDD/Fs were observed during winter, followed by spring, autumn and summer. Atmospheric PCDD/Fs and DL-PCBs in South Korea rapidly decreased during the last 10 years (1998-2008), demonstrating the efficiency of stricter regulations and the application of best available technologies/best environmental practices at emission sources. Comparison of the congener profiles and principal component analysis showed that current atmospheric PCDD/Fs are mostly influenced by industrial sources and PCBs from old commercial PCB uses. Nationwide POPs monitoring will continue and allows an effective evaluation of the implementation of the Stockholm Convention on POPs. 相似文献
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The effect of polarity on the oxidation of Hg0 was examined in the presence of O2 via a pulsed corona discharge (PCD). The experimental result showed no difference in the energy yield of Hg0 oxidation at both positive and negative PCDs (∼8 μg Hg W h−1 at following conditions: total flow rate = 2 L min−1 (Hg0 = 50 μg N m−3, O2 = 10%, and N2 balance), temperature = 150 °C, and specific energy density = 5-15 W h N m−3). This suggests that the positive PCD process used to control gaseous air pollutants may play an essential key role in Hg0 oxidation because it consumes enough energy (∼15 W h N m−3) but an electrical precipitator could not because it consumes less energy (∼0.3 W h N m−3) to oxidize Hg0. 相似文献
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Shin D Moon HS Lin CC Barkay T Nam K 《Environmental pollution (Barking, Essex : 1987)》2011,159(2):509-514
A phenanthrene-degrading bacterium, Sphingomonas paucimobilis EPA505 was used to construct two fluorescence-based reporter strains. Strain D harboring gfp gene was constructed to generate green fluorescence when the strain started to biodegrade phenanthrene. Strain S possessing gef gene was designed to die once phenanthrene biodegradation was initiated and thus to lose green fluorescence when visualized by a live/dead cell staining. Confocal laser scanning microscopic observation followed by image analysis demonstrates that the fluorescence intensity generated by strain D increased and the intensity by strain S decreased linearly at the phenanthrene concentration of up to 200 mg/L. Such quantitative increase and decrease of fluorescence intensity in strain D (i.e., from 1 to 11.90 ± 0.72) and strain S (from 1 to 0.40 ± 0.07) were also evident in the presence of Ottawa sand spiked with the phenanthrene up to 1000 mg/kg. The potential use of the reporter strains in quantitatively determining biodegradable or toxic phenanthrene was discussed. 相似文献
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