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41.
本文基于渤海海峡北部沿岸一观测站点长时间序列海流观测数据分析了海峡北部沿岸流的季节变化特征。冬夏两季余流平均流速均呈现表层最大,中层最小,底层较中层略微增大的分布态势。冬夏底层余流均存在跨等深线向岸的分量,表明底层水向岸的运动是两季都存在的现象。对余流用矢量经验正交分解得到的第一模态空间分量显示,两季余流主要是沿着等深线变化的,冬季各层余流主体变化步调一致,夏季表层与其他各层变化位相相反。风应力是引起余流变化的因素之一,但并不是主要因素。交叉谱分析亦表明,冬季余流变化滞后风应力18 h,与风应力在周期为6 d的波动成分上相关性显著;夏季余流变化滞后风应力9 h,与风应力在周期为0.8 d的波动成分上相关性显著。 相似文献
42.
Zheng Yali He Xiaoyi Wang Hewu Wang Michael Zhang Shaojun Ma Dong Wang Binggang Wu Ye 《Mitigation and Adaptation Strategies for Global Change》2020,25(3):355-370
Mitigation and Adaptation Strategies for Global Change - Electric vehicles (EVs) play a crucial role in addressing climate change and urban air quality concerns. China has emerged as the global... 相似文献
43.
Long Xingle Sun Chuanwang Wu Chao Chen Bin Boateng Kofi Agyenim 《Mitigation and Adaptation Strategies for Global Change》2020,25(7):1243-1260
Mitigation and Adaptation Strategies for Global Change - Considering government and market failure of environmental regulation to combat increasing GHG (greenhouse gas) emissions, green innovation... 相似文献
44.
根据深圳市龙华区观澜子站空气质量监测数据,对龙华区近年来空气质量状况、主要大气污染物浓度时间变化特征、气象条件和污染物浓度相关性,以及典型臭氧(O_3)污染过程进行了分析。结果表明龙华区空气质量以优良为主,空气质量指数(AQI)超标日中,O_3浓度超标天数最多,其次依次是PM_(2.5)、PM_(10)和二氧化氮(NO_2)。PM_(2.5)、PM_(10)和NO_2在秋冬季的浓度最高,春季次之,夏季最低;而O_3浓度则在夏秋季最高,春季次之,冬季最低。除O_3(日间浓度高于夜间浓度)以外,PM_(2.5)、PM10和NO_2晚间浓度高于日间浓度。此外,相关性研究表明,颗粒物污染以细颗粒物为主,O_3(8 h)和NO_2与颗粒物浓度均呈正相关性。由于地域差异的存在,O_3(8 h)和颗粒物浓度的相关性在不同地域表现也不同。同时,大气污染物浓度与气象条件和人为排放源的相关性较高。 相似文献
45.
采用两步水热法制备了新型磁性纳米Fe3O4@α-MnO2复合材料作为催化剂,用于活化过一硫酸盐(PMS)产生强氧化性的硫酸根自由基(SO4-·)氧化降解偶氮染料活性黑5(RBK5).采用透射电子显微镜(TEM),X射线粉末衍射仪(XRD)和振动样品磁强计(VSM)对制备的催化剂进行表征,证明成功合成了纳米α-MnO2包覆Fe3O4形态的Fe3O4@α-MnO2催化剂,催化剂的饱和磁化强度为39.89emu/g.Fe3O4@α-MnO2催化剂活化PMS与单一的Fe3O4和α-MnO2活化PMS相比,具有更高的催化效率,说明铁锰双金属存在协同作用.同时研究了催化剂的投加量、PMS的浓度和初始pH值等各种因素对RBK5的降解效率以及反应动力学的影响.实验结果表明,Fe3O4@α-MnO2催化剂活化PMS降解RBK5的过程符合准一级反应动力学,在催化剂投加量为1.2g/L,PMS的浓度为4mmol/L,初始pH值为7.0,反应时间为60min的情况下,浓度为30mg/L的RBK5的降解效率可达到91%,此时RBK5的降解速率常数也达到最高值0.023min-1.此外,通过加入自由基淬灭剂甲醇、叔丁醇和硝基苯判断了Fe3O4@α-MnO2/PMS体系中起主要氧化降解作用的活性物种为SO4-·. 相似文献
46.
Zhuofei Du Min Hu Jianfei Peng Song Guo Rong Zheng Jing Zheng Dongjie Shang Yanhong Qin He Niu Mengren Li Yudong Yang Sihua Lu Yusheng Wu Min Shao Shijin Shuai 《环境科学学报(英文版)》2018,30(4):348-357
Light-duty gasoline vehicles have drawn public attention in China due to their significant primary emissions of particulate matter and volatile organic compounds(VOCs). However,little information on secondary aerosol formation from exhaust for Chinese vehicles and fuel conditions is available. In this study, chamber experiments were conducted to quantify the potential of secondary aerosol formation from the exhaust of a port fuel injection gasoline engine. The engine and fuel used are common in the Chinese market, and the fuel satisfies the China V gasoline fuel standard. Substantial secondary aerosol formation was observed during a 4–5 hr simulation, which was estimated to represent more than 10 days of equivalent atmospheric photo-oxidation in Beijing. As a consequence, the extreme case secondary organic aerosol(SOA) production was 426 ± 85 mg/kg-fuel, with high levels of precursors and OH exposure. The low hygroscopicity of the aerosols formed inside the chamber suggests that SOA was the dominant chemical composition. Fourteen percent of SOA measured in the chamber experiments could be explained through the oxidation of speciated single-ring aromatics. Unspeciated precursors, such as intermediate-volatility organic compounds and semi-volatile organic compounds, might be significant for SOA formation from gasoline VOCs. We concluded that reductions of emissions of aerosol precursor gases from vehicles are essential to mediate pollution in China. 相似文献
47.
Zhixiang Zhou Tong Shao Mengnan Qin Xiaoyan Miao Yu Chang Wang Sheng Fengshang Wu Yunjiang Yu 《环境科学学报(英文版)》2018,30(4):182-187
The purpose of this study was to examine the direct toxicity of PM2.5 collected from Beijing on human umbilical vein endothelial cells(HUVEC). A Cell Counting Kit 8(CCK8) assay demonstrated that PM2.5 exposure decreased the proliferation of HUVECs in a dosedependent manner. We also found that PM2.5 exposure induced autophagy in HUVECs, as evidenced by:(1) an increased number of double-membrane vesicles;(2) enhanced conversion and punctuation of the microtubule-associated protein light chain 3(LC3); and(3) decreased levels of the selective autophagy substrate p62 in a time-dependent manner.Furthermore, promoting autophagy in PM2.5-exposed HUVECs with rapamycin increased the cell survival rate, whereas inhibiting autophagy via 3-methyladenine significantly decreased cell survival. These results demonstrate that PM2.5 exposure can induce cytotoxicity and autophagy in HUVECs and that autophagy play a protective role against PM2.5-induced cytotoxicity. The findings of the present study imply a direct toxic effect of PM2.5 on HUVECs and provide novel insight into the mechanism of cardiovascular diseases caused by PM2.5 exposure. 相似文献
48.
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
49.
Xiuzheng Zhuang Yanqin Huang Huacai Liu Hongyou Yuan Xiuli Yin Chuangzhi Wu 《环境科学学报(英文版)》2018,30(7):261-270
Sewage sludge (SS) and deinking sludge (DS) were used to comparatively study the hydrothermal dewatering of sludge with different components. For a better overview, an insight into the relationship between physicochemical properties and dewaterability of hydrothermal sludge was provided. Results found that not all kinds of sludge were suitably conditioned by hydrothermal treatment (HT) in term of the elevation of dewaterability. Higher hydrothermal temperature tended to enhance the dewaterability of SS rather than DS, which was supported by the variation of their physicochemical properties (including water distribution, bonding energy, extracellular polymeric substance (EPS), particles size, acid functional groups and zeta potential in this study). In addition, the changes in surface morphology suggested that the reverse effect of HT on sludge dewaterability was mainly due to their dewatering behavior. For SS, the destruction of EPS structure leaded to the release of bound water, thereby strengthening sludge dewatering. Conversely, “Bridging effect” generated by lignocellulose in DS was beneficial for sludge dewatering; however, the increasing hydrothermal temperature degraded part of lignocellulose and weakened “bridging effect”, finally resulting in worse dewaterability of DS. 相似文献
50.
Yanqin Ren Gehui Wang Jianjun Li Can Wu Cong Cao Jiayuan Wang Lu Zhang Fan Meng Hong Li 《环境科学学报(英文版)》2018,30(9):32-44
Size-resolved biogenic secondary organic aerosols(BSOA) derived from isoprene and monoterpene photooxidation in Qinghai Lake, Tibetan Plateau(a continental background site) and five cities of China were measured using gas chromatography/mass spectrometry(GC/MS). Concentrations of the determined BSOA are higher in the cities than in the background and are also higher in summer than in winter. Moreover, strong positive correlations(R2= 0.44–0.90) between BSOA and sulfate were found at the six sites,suggesting that anthropogenic pollution(i.e., sulfate) could enhance SOA formation,because sulfate provides a surface favorable for acid-catalyzed formation of BSOA. Size distribution measurements showed that most of the determined SOA tracers are enriched in the fine mode( 3.3 μm) except for cis-pinic and cis-pinonic acids, both presented a comparable mass in the fine and coarse( 3.3 μm) modes, respectively. Mass ratio of oxidation products derived from isoprene to those from monoterpene in the five urban regions during summer are much less than those in Qinghai Lake region. In addition, in the five urban regions relative abundances of monoterpene oxidation products to SOA are much higher than those of isoprene. Such phenomena suggest that BSOA derived from monoterpenes are more abundant than those from isoprene in Chinese urban areas. 相似文献