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排序方式: 共有2303条查询结果,搜索用时 15 毫秒
1.
Tang Zhi Li Yilian Yang Zhe Liu Danqing Tang Min Yang Sen Tang Ye 《Environmental science and pollution research international》2019,26(20):20277-20285
Environmental Science and Pollution Research - The sorption/desorption behaviors of benzene, toluene, ethylbenzene, and xylene (BTEX) on soil organic matter (SOM) have a significant influence on... 相似文献
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Feng Jingchun Tang YunQing Xue Song Zhang Ke 《Environment, Development and Sustainability》2022,24(1):138-155
Environment, Development and Sustainability - The PPP mode of rural water environment governance was conducive to attracting social capital for giving full play to the decisive role of the market... 相似文献
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Xue Han Xin Ji Xuan M Jun-Ling Liu Zhen-Yu He Wei Chang Fei Tang Ai-Lin Liu 《环境科学学报(英文版)》2020,32(1):310-318
Changes in water quality from source water to finished water and tap water at two conventional drinking water treatment plants(DWTPs) were monitored.Beside the routine water quality testing,Caenorhabditis elegans-based toxicity assays and the fluorescence excitation–emission matrices technique were also applied.Both DWTPs supplied drinking water that met government standards.Under current test conditions,both the investigated finished water and tap water samples exhibited stronger lethal,genotoxic and reprotoxic potential than the relative source water sample,and the tap water sample was more lethal but tended to be less genotoxic than the corresponding finished water sample.Meanwhile,the nearly complete removal of tryptophan-like substances and newly generated tyrosine-like substances were observed after the treatment of drinking water,and humic-like substances were identified in the tap water.Based on these findings,toxic pollutants,including genotoxic/reproductive toxicants,are produced in the drinking water treatment and/or distribution processes.Moreover,further studies are needed to clarify the potentially important roles of tyrosine-like and humic-like substances in mediating drinking water toxicity and to identify the potential sources of these contaminants.Additionally,tryptophan-like fluorescence may be adopted as a useful parameter to monitor the treatment performance of DWTPs.Our observations provided insights into the importance of utilizing biotoxicity assays and fluorescence spectroscopy as tools to complement the routine evaluation of drinking water. 相似文献
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The degradation of pharmaceutical micropollutants is an intensifying environmental problem and synthesis of efficient photocatalysts for this purpose is one of the foremost challenges worldwide. Therefore, this study was conducted to develop novel plasmonic Ag/Ag2O/BiVO4 nanocomposite photocatalysts by simple precipitation and thermal decomposition methods, which could exhibit higher photocatalytic activity for mineralized pharmaceutical micropollutants. Among the different treatments, the best performance was observed for the Ag/Ag2O/BiVO4 nanocomposites (5 wt.%; 10 min's visible light irradiation) which exhibited 6.57 times higher photodegradation rate than the pure BiVO4. Further, the effects of different influencing factors on the photodegradation system of tetracycline hydrochloride (TC-HCl) were investigated and the feasibility for its practical application was explored through the specific light sources, water source and cycle experiments. The mechanistic study demonstrated that the photogenerated holes (h+), superoxide radicals (?O2?) and hydroxyl radicals (?OH) participated in TC-HCl removal process, which is different from the pure BiVO4 reaction system. Hence, the present work can provide a new approach for the formation of novel plasmonic photocatalysts with high photoactivity and can act as effective practical application for environmental remediation. 相似文献
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土壤多酚氧化酶是一种氧化还原酶,能够将土壤中芳香族化合物氧化成醌,促进土壤中石油类物质的分解转化.以距大庆油田工作区不同距离(1、5、15 km)的石油污染地为对象,研究不同温度下石油污染裸地及羊草(Leymus chinensis)修复地的土壤多酚氧化酶活性及其动力学和热力学特征的变化.结果表明:土壤多酚氧化酶活性随温度和底物浓度的增加而逐渐增大,在温度为30℃或40℃、底物浓度为80 mmol/L或160 mmol/L时达到最大值;各样地土壤酶的动力学参数Km(Mihaelis常数)随温度的变化规律不同,Vmax(酶促反应最大速度)和Vmax/Km(催化效率)随温度升高而逐渐增大,均在30℃或40℃时达到最大值;热力学参数Q10(温度系数)、ΔH(活化焓)、ΔS(活化熵)随温度变化差异不显著,ΔG(活化自由能)随温度升高呈逐渐增加趋势.在同一温度下,石油污染裸地土壤多酚氧化酶活性高于羊草修复地;Km和Vmax/Km在各样地均表现为无规律性变化,Vmax最大值出现在距油田工作区5 km处的裸地(BMP),最小值出现在距油田工作区5 km处的羊草修复地(LMP);Q10、Ea(活化能)、ΔH、ΔS的最大值均出现在距油田工作区1 km处的裸地(BVP),最小值均出现在距油田工作区1 km处的羊草修复地(LVP).研究显示,升温和植物修复对土壤多酚氧化酶活性的反应特征有较大影响. 相似文献
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Qingru Wu Shuxiao Wang Mei Yang Haitao Su Guoliang Li Yi Tang Jiming Hao 《环境科学学报(英文版)》2018,30(6):91-99
Large-scale gold production(LSGP) is one of the five convention-related atmospheric mercury(Hg) emission sources in the Minamata Convention on Mercury. However, field experiments on Hg flows of the whole process of LSGP are limited. To identify the atmospheric Hg emission points and understand Hg emission characteristics of LSGP, Hg flows in two gold smelters were studied. Overall atmospheric Hg emissions accounted for 10%–17% of total Hg outputs and the Hg emission factors for all processes were 7.6–9.6 kg/ton. There were three dominant atmospheric Hg emission points in the studied gold smelters, including the exhaust gas of the roasting process, exhaust gas from the environmental fog collection stack and exhaust gas from the converter of the refining process. Atmospheric Hg emissions from the roasting process only accounted for 16%–29% of total emissions and the rest were emitted from the refining process. The overall Hg speciation profile(gaseous elemental Hg/gaseous oxidized Hg/particulate-bound Hg) for LSGP was 34.1/57.1/8.8. The dominant Hg output byproducts included waste acid, sulfuric acid and cyanide leaching residue. Total Hg outputs from these three byproducts were 80% in smelter A and 84% in smelter B. Our study indicated that previous atmospheric Hg emissions from large-scale gold production might have been overestimated.Hg emission control in LSGP is not especially urgent in China compared to other significant emission sources(e.g., cement plants). Instead, LSGP is a potential Hg release source due to the high Hg output proportions to acid and sludge. 相似文献