全文获取类型
收费全文 | 167篇 |
免费 | 25篇 |
国内免费 | 234篇 |
专业分类
安全科学 | 6篇 |
废物处理 | 11篇 |
环保管理 | 5篇 |
综合类 | 258篇 |
基础理论 | 53篇 |
污染及防治 | 91篇 |
评价与监测 | 2篇 |
出版年
2024年 | 1篇 |
2023年 | 9篇 |
2022年 | 9篇 |
2021年 | 16篇 |
2020年 | 24篇 |
2019年 | 25篇 |
2018年 | 21篇 |
2017年 | 16篇 |
2016年 | 27篇 |
2015年 | 18篇 |
2014年 | 21篇 |
2013年 | 32篇 |
2012年 | 21篇 |
2011年 | 21篇 |
2010年 | 12篇 |
2009年 | 12篇 |
2008年 | 12篇 |
2007年 | 20篇 |
2006年 | 24篇 |
2005年 | 13篇 |
2004年 | 16篇 |
2003年 | 11篇 |
2002年 | 8篇 |
2001年 | 6篇 |
2000年 | 8篇 |
1999年 | 7篇 |
1998年 | 5篇 |
1997年 | 4篇 |
1996年 | 3篇 |
1995年 | 1篇 |
1994年 | 2篇 |
1991年 | 1篇 |
排序方式: 共有426条查询结果,搜索用时 46 毫秒
121.
采用高效液相色谱对电化学氧化除氨氮过程,不同电流密度,Cl-浓度及初始pH值的·OH进行定量检测和分析,同时,对不同初始pH值和电流密度下,电化学氧化除氨氮的中间产物进行了定量分析,结果表明:·OH产生量与电流密度成正比,当有Cl-存在,且在碱性条件下会抑制·OH的产生;初始pH值为偏碱性时,NO2-和氯胺的产量均有所增加.建议电化学氧化脱氨氮过程,尽量保持溶液pH值在中性或酸性条件下;电流密度对氨氮电化学氧化过程中各中间产物的量有着较大影响,在电流密度为10mA/cm2时,活性物质产量最高,且有害中间产物产量最低. 相似文献
122.
Xiang ZHANG Xiaogang GU Shuguang LU Zhouwei MIAO Minhui XU Xiaori FU Muhammad DANISH Mark L. BRUSSEAU Zhaofu QIU Qian SUI 《Frontiers of Environmental Science & Engineering》2016,10(3):502-512
Trichloroethene (TCE) degradation by Fe(III)-activated calcium peroxide (CP) in the presence of citric acid (CA) in aqueous solution was investigated. The results demonstrated that the presence of CA enhanced TCE degradation significantly by increasing the concentration of soluble Fe(III) and promoting H2O2 generation. The generation of HO? and O2-? in both the CP/Fe(III) and CP/Fe(III)/CA systems was confirmed with chemical probes. The results of radical scavenging tests showed that TCE degradation was due predominantly to direct oxidation by HO?, while O2-? strengthened the generation of HO? by promoting Fe(III) transformation in the CP/Fe(III)/CA system. Acidic pH conditions were favorable for TCE degradation, and the TCE degradation rate decreased with increasing pH. The presence of Cl-, HCO3-, and humic acid (HA) inhibited TCE degradation to different extents for the CP/Fe(III)/CA system. Analysis of Cl- production suggested that TCE degradation in the CP/Fe(III)/CA system occurred through a dechlorination process. In summary, this study provided detailed information for the application of CA-enhanced Fe(III)-activated calcium peroxide for treating TCE contaminated groundwater. 相似文献
123.
A treatability study was conducted to determine the potential of white rot fungi to remediate soil from a Superfund site that had been contaminated with DDT. A tiered approach was utilized, starting with simple laboratory studies to screen the potential of white rot fungal strains to degrade DDT and culminating with a soil pan study that simulated land farming. Results from early tiers of the study indicated that Phanerochaete sordida had the best potential for remediating the soil. In the soil pan study, the fungus ultimately grew very well after second inoculation. However, the good growth did not translate to higher DDT removal compared to removal in pans that were not inoculated. 14[DDT] fate studies indicated the small amount of removal that did occur for both fungal inoculated and non‐inoculated conditions could be partially attributed to incorporation into humic material. Addition of a surfactant to the soil enhanced the removal of DDT in both inoculated and non‐inoculated soil. Consequently, under simulated land fanning conditions, this strain of fungus was not successful in remediating this soil. 相似文献
124.
Oxidative stress parameters and some antioxidant defense systems in the liver of Carassius auratus exposed to glyphosate and its formulation (Roundup®) have been studied. Fish were exposed to glyphosate and its formulation at concentrations of 0.032, 0.16, 0.8, and 4.0 mg L?1, all calculated on glyphosate basis, for 11 days. Hydroxyl radical generation as determined by electron spin resonance spectroscopy of its spin-adduct with α-phenyl-t-butyl nitrone increased with the concentration of Roundup®. Superoxide dismutase activities were decreased relative to control by 21%–46% when exposed to glyphosate and 45%–52% when exposed to Roundup®, suggesting that the formulation is more toxic than glyphosate alone. Catalase showed no difference between both groups. 相似文献
125.
126.
氯自由基(·Cl)的高氧化性及其内陆来源的新发现使得·Cl在评估有机污染物的大气归趋方面起着比以往更为重要的作用。含有NH_x(x=1,2)结构的有机化合物不仅是大气中一类潜在的有机污染物,也是大气中致癌性亚硝胺的前驱体—N中心自由基的重要来源。前人研究发现,·Cl与含有NH_x(x=1,2)结构的有机化合物具有独特的相互作用且其反应具有结构依赖性。目前,大多数研究只关注链状含有NH_x(x=1,2)结构有机化合物的反应,而对于环状含有NH结构有机化合物的反应研究却很少。本研究使用量子化学和动力学模拟相结合的方法研究·Cl引发3种环状含有NH结构有机化合物(吗啉(MOR)、哌啶(PIP)和吡咯烷(PYR))的大气转化机制及动力学。结果发现,·Cl夺取3种环状含有NH结构有机化合物中N—H的H原子形成N中心自由基是最可行的反应路径。在298 K和1 atm下,计算的反应速率常数分别为5.0!10-10(MOR)、5.1!10-10(PIP)和4.9!10-10(PYR) cm~3·molecule-1·s-1,且具有正的温度依附性。结合可获得的·OH引发反应的反应速率常数,评估·Cl对MOR和PIP转化的贡献分别为·OH的2.6%~26%和6.9%~69%。上述研究结果为将来建立·Cl引发含有NH_x(x=1,2)结构有机化合物反应的结构-活性关系、全面评估含有NH_x(x=1,2)结构有机化合物的大气归趋和环境风险提供数据支持。 相似文献
127.
Virender K. Sharma Xin Yu Thomas J. McDonald Chetan Jinadatha Dionysios D. Dionysiou Mingbao Feng 《Frontiers of Environmental Science & Engineering》2019,13(3):37
128.
为了解决目前气体电离放电脱硫方法存在的等离子源体积庞大、能耗高、以及需要依靠传统脱硫方法的协同作用等问题.拟用小流量高浓度氧活性粒子[O2+、O(1D)、O(3P)、O3]及引发剂HO2-分别注入烟道中,与烟气中H2O反应生成·OH;在无吸收剂、无催化剂及没有其他技术协同作用下,进行·OH氧化脱除大烟气量中的微量SO2并生成H2SO4的实验.结果表明:烟气温度为30℃,氧活性粒子与SO2摩尔比为3~4时,脱硫率达到94.6%,回收酸液中SO42-浓度达到9.3g/L. 相似文献
129.
Scott Elliott Gerald E. Streit Jeffrey S. Gaffney James E. Bossert Michael Brown Jon Reisner Laurie A. McNair 《Environmental science and pollution research international》1999,6(2):103-105
The nerve agent sarin has recently been deployed by terrorists in a major city. The molecule is volatile and made its way
to many victims by passing as vapor through a highly reactive medium. Here we estimate rates and pathways for the removal
of gas phase sarin from a generalized urban atmosphere. Only information from the open scientific literature is used. By structure
reactivity comparisons with the organophosphorus pesticides, hydroxyl radical hydrogen abstraction may occur in as little
as one hour. Decomposition of side chains after hydroxyl attack leads to organic oxygenates which preserve the phosphonofluoridate
and so toxicity. The aqueous aerosol surface is contacted in minutes and offers access to a range of dissolved nucleophiles.
Substitution displaces the fluoride leaving group, giving safe phosphoric acid analogs. Because of uncertainties in the electron
distribution and in aqueous decay mechanisms, the time constants must be viewed as lower limits. 相似文献
130.
长光路FTIR研究OH发生体系中的OH浓度 总被引:2,自引:0,他引:2
利用长光路FTIR测定早苯、三本等芳香烃化合物在烟雾箱中光化学反应衰减,确字了NOx-H2O、Air、HONO-H2O-Air和CH3ONO-NO-Air3种体系在我灯自夸下的OH浓度,结果表明三者OH浓度范围分别为:~10^5~10^6、~10^7、~10^7~10^8molecules.cm^-3,并进一步讨论了反应前体物对生成OH浓度的影响。 相似文献