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561.
Luo W Lu Y Wang B Tong X Wang G Shi Y Wang T Giesy JP 《Environmental monitoring and assessment》2009,158(1-4):507-517
Fifty-seven typical surface soils and 108 deeper soils were collected from five former industrial sites in Beijing and concentrations of total Hg (SigmaHg) as well as pH, total carbon (TC), total nitrogen (TN), total sulfur, and dissolved organic carbon concentrations determined. The mean concentration of SigmaHg in surface soils was significantly greater than background concentrations in the vicinity of Beijing. Forty-eight percent of the samples exceeded the "critical" concentration of 1.0 mg Hg/kg, dry weight in soils, which has been established by the Chinese government. At depths of 0-80 cm in the soil, profile concentrations of SigmaHg also exceeded the background value. There were significant correlations between concentrations of SigmaHg, TC, and TN in the industrial soils. The greater concentration of SigmaHg in most soils could have been due in part to combustion of coal and leakage from industrial processes. 相似文献
562.
Tao Chuanjiang Li Dahui Zhang Xinzhong Chen Shanshan Fu Lijuan Piao Xiuying Shi Jie Jiang Hui Li Chongjiu Li Jianzhong 《Environmental monitoring and assessment》2010,165(1-4):685-692
To analysze the dynamic degradation and final residues of acephate and its metabolite methamidophos, field-experiments with pakchoi (Brassica campestris L.) in open field and greenhouse were carried out in Beijing, China in 2004 and 2005. The degradation dynamics and final residues were determined by gas chromatography (GC) equipped with a pulsed flame photometric detector and GC coupled to mass spectrometry (MS)/MS after acephate was applied on open field and green house pakchoi (B. campestris L.). The dynamic degradation results showed that the half-lives of acephate and methamidophos in open field pakchoi were 1.36 days with dynamic degradation equation C t ?=?133.01e???0.5107t , and 2.86 days with C t ?=?6.5753e???0.2422t , respectively. While the half-lives of acephate and methamidophos in the greenhouse were 1.07 days with C t ?=?59.134e???0.4353t and 0.79 days with C t ?=?0.2703e???0.2595t , respectively. The final residue analysis demonstrated that >50% of total methamidophos were resulted from the degradation of acephate 7 and 18 days after it was applied on the greenhouse pakchoi, respectively. While in the open-field pakchoi, >90% of total methamidophos was found to be the metabolite of acephate. 相似文献
563.
Size and resin fractionations of dissolved organic matter and trihalomethane precursors from four typical source waters in China 总被引:3,自引:0,他引:3
Wei Q Wang D Wei Q Qiao C Shi B Tang H 《Environmental monitoring and assessment》2008,141(1-3):347-357
Dissolved organic matter (DOM) and its potential to form disinfection by-products (DBPs) during drinking water treatment raise
challenges to water quality control. Understanding both chemical and physical characteristics of DOM in source waters is key
to better water treatment. In this study, the DOM from four typical source waters in China was fractionated by XAD resin adsorption
(RA) and ultrafiltration (UF) techniques. The trihalomethane formation potential (THMFP) of all fractions in the DOM were
investigated to reveal the major THM precursors. The fraction distributions of DOM could be related to their geographical
origins in a certain extent. The dominant chemical fraction as THM precursors in the DOM from south waters (East-Lake reservoir
in Shenzhen and Peal rivers in Guangzhou) was hydrophobic acid (HoA). The size fraction with molecular weight (MW) <1 kDa
in both south waters had the highest THMFP. The results of cluster analysis showed that the parameters of fractions including
DOC percentage (DOC%), UV254%, SUVA254 (specific UV254 absorbance) and THMFP were better for representing the differences of DOM from the studied waters than specific THMFP (STHMFP).
The weak correlation between SUVA254 and STHMFP for either size or XAD fractions suggests that whether SUVA254 can be used as an indicator for the reactivity of THM formation is highly dependent on the nature of organic matter. 相似文献
564.
Farming Endangered Turtles to Extinction in China 总被引:1,自引:0,他引:1
565.
运输应激对二花脸和皮特兰猪血浆应激和代谢相关激素水平的影响 总被引:3,自引:0,他引:3
比较二花脸和皮特兰猪在2h运输过程中血浆ACTH、皮质醇、胰岛素和T3、T4水平的动态变化模式,以分析内分泌激素变化的品种特征.选用雄性二花脸猪10头,皮特兰猪6头,体重达20kg时安装颈静脉瘘管,1wk后运输试验,运输过程中不同时间点采集血样,放射免疫分析法测定血浆激素水平.上车后两品种猪ACTH水平缓慢上升,60min后达到峰值,下车后15min恢复至基础水平,运输过程中ACTH水平及变化幅度均未表现显著的品种差异;运输前皮质醇水平二花脸显著高于皮特兰猪,上车后两品种皮质醇均迅速上升,出发后15min达到峰值,下车后15min均快速恢复至基础水平,运输过程中皮特兰皮质醇上升的幅度显著高于二花脸猪;两品种胰岛素水平上车后均呈下降趋势,二花脸胰岛素水平总体上显著高于皮特兰猪;T3水平在上车后也表现快速下降,无论是T3水平还是其变化幅度均不表现显著的品种差异;皮特兰猪上车后T4水平稍微下降而二花脸猪显著下降,皮特兰T4水平总体显著高于二花脸猪.运输应激伴随血浆ACTH和皮质醇水平升高,而胰岛素、T3和T4水平下降,皮质醇水平升高的幅度能够反映猪的应激敏感性.图1参25 相似文献
566.
Fifty-six representative samples of topsoil were collected around Guanting Reservoir, which is an important water source for
Beijing. Concentrations of the insecticides HCH, DDT, and their metabolites were quantified by use of gas chromatography (GC)
with electron capture detection (ECD). Organochlorine pesticides (OCPs) are still present in surface soils in the Guanting
area. DDT accounts for about 93% of the total OCP content. Concentrations of α/γ, β/γ, and DDT/DDE are the result not only
of historical use, but also of more recent depositions. Statistical analyses, including principal component analysis (PCA)
and cluster analysis (CA), revealed associations between concentrations of OCPs and major soil characteristics. Geographical
information system (GIS) technology was used to develop maps of the distributions of OCP concentrations. The areas of greatest
contamination were primarily in the central part of the study area and were correlated with greater population density, heavier
traffic, and more industrial activity. 相似文献
567.
Effects of land use on concentrations of metals in surface soils and ecological risk around Guanting Reservoir,China 总被引:7,自引:0,他引:7
Luo W Lu Y Giesy JP Wang T Shi Y Wang G Xing Y 《Environmental geochemistry and health》2007,29(6):459-471
It is accepted that the historical routine use of agrochemicals may have resulted in undesirable concentrations of metals
in the environment. To investigate and assess the effects of land use on concentrations of heavy metals around the Guanting
Reservoir in China, 52 surface soil samples (depth of 2–10 cm) were taken from areas where four types of land use were practiced
(including arable land, woodland, bare land, orchard land). The metals and metalloids (As, Cr, Ni, Cu, Zn, Cd, and Pb) were
analyzed using inductively coupled plasma-atomic emission spectroscopy (ICP-AES). Significant accumulation of As, Cd, and
Cr was found in soils of arable land. Based on correlation and cluster analysis, it can be concluded that Cd and Zn originate
mainly from phosphate fertilizer, Pb from the use of insecticides, fertilizers, and sewage sludge as well as air deposition,
and Cu from copper-based fungicides, while As, Ni and Cr might come from parent soil material. According to an ecological
risk analysis of metals based on the ecological index suggested by Hakanson, the four types of land can be ranked by severity
of ecological risk as follows: arable land > woodland > bare land > orchard land, with a high ecological risk of Cd for all
four types. Management measures for land use planners for avoiding water, soil, and sediment pollution caused by metals around
the Guanting Reservoir are presented. 相似文献
568.
采用共沉淀法制备了一种新型催化剂——铁铈钛复合氧化物催化剂,研究了Fe掺加量、体积空速以及H2O和SO2的加入对其选择性催化还原NO性能的影响;采用XRD和SEM等手段对催化剂的结构和形貌进行了表征。表征结果显示,Fe的掺加使催化剂表面的颗粒更均匀,提高了催化剂的分散度。实验结果表明:以Ce(NO3)3,Fe(NO3)3?9H2O,TiOSO4?2H2O为原料、按n(Ce)∶n(Fe)∶n(Ti)=0.2∶0.8∶1配比制得的Ce0.2Fe0.8TiOx为催化剂,在反应温度250 ℃、反应时间3 h、体积空速25 000 h-1的条件下,NO去除率为99.8%,N2选择性为100%;Fe的掺加显著提高了Ce0.2Fe0.8TiOx催化剂的抗H2O和SO2的能力。 相似文献
569.
采用向十三烷基苯磺酸钠(STBS)和非离子表面活性剂辛基酚聚氧乙烯醚(OP-10)二元复配溶液中添加β-环糊精(β-CD)的方法,降低STBS和OP-10之间定量检测时的相互干扰。实验结果表明:添加β-CD时,可提高STBS的检测准确性,降低STBS对OP-10的检测干扰;在二元复配溶液中,STBS和OP-10的方法回收率分别在100.8%~102.0%,97.4%~102.2%之间,检测误差分别在2.0%和2.6%以内;Cl-,SO42-,Na+,Ca2+的存在对二元复配溶液中STBS和OP-10的检测干扰可忽略;将该方法应用于地层水水样中,仍可准确定量分析STBS和OP-10的含量。 相似文献
570.
以自制铋电极作为工作电极,建立了铋电极差分脉冲伏安法测定2,4-二硝基苯肼的分析方法。实验结果表明:以0.1 mol/L NaOH+0.1 mol/L KCl混合溶液(pH=13.0)配制测定底液,在扫描速率为100 mV/s的条件下,2,4-二硝基苯肼于-0.53 V处产生灵敏的氧化峰;在2,4-二硝基苯肼浓度为3.0×10-8~1.0×10-5 mol/L范围内,空白和试样的氧化峰电流强度差值与对应2,4-二硝基苯肼浓度的对数呈良好的线性关系,检出限达8.37×10-9 mol/L;将该方法应用于工业废水中痕量2,4-二硝基苯肼的检测,回收率为95.6%~103.1%,相对标准偏差小于3%。 相似文献