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101.
102.
Yuanhang Zhang Yuesi Wang Xin Jin Zirui Liu Gehui Wang Guiqian Tang Keding Lu Bo Hu Shanshan Wang Guohui Li Xinqin An Chao Wang Qihou Hu Lingyan He Fenfen Zhang 《环境科学学报(英文版)》2023,123(1):350-366
Atmospheric oxidizing capacity (AOC) is an essential driving force of troposphere chemistry and self-cleaning, but the definition of AOC and its quantitative representation remain uncertain. Driven by national demand for air pollution control in recent years, Chinese scholars have carried out studies on theories of atmospheric chemistry and have made considerable progress in AOC research. This paper will give a brief review of these developments. First, AOC indexes were established that represent apparent atmospheric oxidizing ability (AOIe) and potential atmospheric oxidizing ability (AOIp) based on aspects of macrothermodynamics and microdynamics, respectively. A closed study refined the quantitative contributions of heterogeneous chemistry to AOC in Beijing, and these AOC methods were further applied in Beijing-Tianjin-Hebei and key areas across the country. In addition, the detection of ground or vertical profiles for atmospheric OH·, HO2·, NO3· radicals and reservoir molecules can now be obtained with domestic instruments in diverse environments. Moreover, laboratory smoke chamber simulations revealed heterogeneous processes involving reactions of O3 and NO2, which are typical oxidants in the surface/interface atmosphere, and the evolutionary and budgetary implications of atmospheric oxidants reacting under multispecies, multiphase and multi-interface conditions were obtained. Finally, based on the GRAPES-CUACE adjoint model improved by Chinese scholars, simulations of key substances affecting atmospheric oxidation and secondary organic and inorganic aerosol formation have been optimized. Normalized numerical simulations of AOIe and AOIp were performed, and regional coordination of AOC was adjusted. An optimized plan for controlling O3 and PM2.5 was analyzed by scenario simulation. 相似文献
103.
Yuanhang Zhang Yanhui Liu Jiayin Li Yufang M Ming Zhou Zhaofeng Tan Limin Zeng Keding Lu 《环境科学学报(英文版)》2023,123(1):522-534
The atmospheric chemical mechanism is an essential component of airshed models used for investigating the chemical behaviors and impacts of species. Since the first tropospheric chemical mechanism was proposed in the 1960s, various mechanisms including Master Chemical Mechanism (MCM), Carbon Bond Mechanism (CBM), Statewide Air Pollution Research Center (SAPRC) and Regional Atmospheric Chemistry Mechanism (RACM) have been developed for different research purposes. This work summarizes the development and applications of these mechanisms, introduces their compositions and lumping methods, and compares the ways the mechanisms treat radicals with box model simulations. CBM can reproduce urban pollution events with relatively low cost compared to SAPRC and RACM, whereas the chemical behaviors of radicals and the photochemical production of ozone are described in detail in RACM. The photolysis rates of some oxygenated compounds are low in SAPRC07, which may result in underestimation of radical levels. As an explicit chemical mechanism, MCM describes the chemical processes of primary pollutants and their oxidation products in detail. MCM can be used to investigate certain chemical processes; however, due to its large size, it is rarely used in regional model simulations. A box model case study showed that the chemical behavior of OH and HO2 radicals and the production of ozone were well described by all mechanisms. CBM and SAPRC underestimated the radical levels for different chemical treatments, leading to low ozone production values in both cases. MCM and RACM are widely used in box model studies, while CBM and SAPRC are often selected in regional simulations. 相似文献
104.
重金属环境背景值是评价环境中重金属污染和制定环境质量标准的前提和基础,为确定厦门西港近岸海域沉积物中重金属元素的背景值水平,以厦门西港近岸海域柱状沉积物样品为研究对象,对不同深度沉积物样品的重金属元素含量进行测定,在分析重金属元素垂直分布特征的基础上,筛选未受人为活动影响的沉积层位,根据数据分布类型计算得到17种重金属元素的背景值(范围):Sc 13. 85(11. 52~16. 69)、V 101. 03(94. 61~107. 45)、Cr 63. 50(55. 00~69. 20)、Co 14. 62(13. 70~15. 54)、Ni 29. 92(27. 23~32. 54)、Cu 21. 48(17. 95~25. 01)、Zn 118. 81(96. 39~141. 23)、Pb 41. 80(38. 41~57. 35)、Sr 97. 78(93. 22~102. 34)、Mo 1. 39(0. 59~2. 19)、Sb 0. 58(0. 53~0. 63)、Ba 407. 00(378. 15~427. 00)、Tl 0. 93(0. 72~1. 05)、Bi 0. 71(0. 51~0. 82)、Fe 32 610. 27(19 903. 73~53 428. 67)、Mn 393. 20(306. 67~793. 63)、Cd 0. 066(0. 056~0. 076) mg/kg。以上背景值与福建省海岸带土壤、厦门A层土壤、中国陆壳、中国浅海沉积物和全国水系沉积物元素背景值相比,总体上比较接近,但Sr含量略低,Pb和Zn含量略高,说明可信度较高且具有地域性。影响厦门西港近岸海域沉积物中重金属元素背景值的主要因素是陆源物质、沉积物粒度和地球化学特征。 相似文献
105.
106.
107.
地下水除草剂阿特拉津污染微生物治理的实验研究 总被引:4,自引:0,他引:4
采用了从农药厂阿特拉津生产车间排污口污泥中分离出的菌种AT菌,进行了农药阿特拉津的静态降解实验及其污染地下水的微生物治理模拟实验研究结果表明,AT菌在pH值为5.0~10.0时对农药污染质阿特拉津均具有降解能力,且适宜的pH值范围为6.5~8.0;在实验条件(t=10℃,pH=7.5)与野外含水层的条件基本一致情况下,难于生物降解的污染质阿特拉津的一次投菌降解率达到31.08%;同时环境因素也随着AT菌作用的变化而变化,其中,DO、pH随AT菌作用加强而其值减小.另外,设计了细菌的投放方式以模拟野外条件下的菌种投加条件.并且AT菌的作用会造成被治理含水层的渗透性能降低,实验后含水层的渗透系数下降60.54%.清水冲洗10d的渗透性恢复率为48.96%,说明清水渗透恢复的方法效果明显. 相似文献
108.
生态技术创新政府启动模式的机理与启示 总被引:2,自引:0,他引:2
生态技术创新是经济可持续发展的必要条件。由于环境资源的公共性,时滞性等特点,政府在生态技术创新过程中发挥重要的作用,是企业生态技术创新的主要推动力。政府启动模式的本 于政府借助法律或经济手段促使企业部分边际外部费用内部化。 相似文献
109.
提出重庆三峡库区实施农林复合经营的重要性及其可持续发展理论和结构类型,并针对存在的问题,提出农林复合经营可持续发展对策。 相似文献
110.